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My functional morphology interests include understanding the relationship between form and function of human and non-human primate postcranial skeleton, with applications to understanding the evolution of early hominin bipedal locomotion. My bioarchaeology interests include understanding mobility patterns and subsistence economies of past populations with particular interest in Southern European Holocenic populations. I apply different approaches to the study of living and fossil human and primate postcranial skeleton. These approaches may include bone cross-sectional analysis, joint analysis, geometric morphometric and muscle structure analysis, and integration of all these data with experimental and in-vivo physiological and observational data. <br />The major part of the projects I am working at involves the use of CT-scanned bones and computer 3D virtual modelling techniques.<br /><span class="u-fw700">Phone: </span>+39 050 2211350<br /><b>Address: </b>Damiano Marchi PhD <br />Department of Biology <br />University of Pisa <br />via Derna, 1 <br />56126 Pisa -Italy <br />Fax:+39 050 2211475<br /><div class="js-profile-less-about u-linkUnstyled u-tcGrayDarker u-textDecorationUnderline u-displayNone">less</div></div></div><div class="ri-section"><div class="ri-section-header"><span>Interests</span><a class="ri-more-link js-profile-ri-list-card" data-click-track="profile-user-info-primary-research-interest" data-has-card-for-ri-list="125165">View All (16)</a></div><div class="ri-tags-container"><a 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href="https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_"><img alt="Research paper thumbnail of The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_">The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)</a></div><div class="wp-workCard_item"><span>American journal of biological anthropology</span><span>, Nov 16, 2021</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ObjectivesLong bone variations during growth are susceptible to the combined action of nutritiona...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067167"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067167"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067167; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067167]").text(description); $(".js-view-count[data-work-id=117067167]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067167; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067167']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067167, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067167]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067167,"title":"The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)","translated_title":"","metadata":{"abstract":"ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.","publisher":"Wiley","publication_date":{"day":16,"month":11,"year":2021,"errors":{}},"publication_name":"American journal of biological anthropology"},"translated_abstract":"ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.","internal_url":"https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_","translated_internal_url":"","created_at":"2024-04-04T06:35:02.337-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9047,"name":"Osteology","url":"https://www.academia.edu/Documents/in/Osteology"},{"id":44744,"name":"Sexual dimorphism","url":"https://www.academia.edu/Documents/in/Sexual_dimorphism"},{"id":85893,"name":"Fibula","url":"https://www.academia.edu/Documents/in/Fibula"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":168987,"name":"Bipedalism","url":"https://www.academia.edu/Documents/in/Bipedalism"}],"urls":[{"id":40844199,"url":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajpa.24440"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067166"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067166/Thigh_and_leg_remains_of_Homo_naledi"><img alt="Research paper thumbnail of Thigh and leg remains of Homo naledi" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067166/Thigh_and_leg_remains_of_Homo_naledi">Thigh and leg remains of Homo naledi</a></div><div class="wp-workCard_item"><span>The 85th Annual Meeting of the American Association of Physical Anthropologists, Atlanta, GA</span><span>, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in So...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067166"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067166"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067166; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067166]").text(description); $(".js-view-count[data-work-id=117067166]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067166; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067166']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067166, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067166]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067166,"title":"Thigh and leg remains of Homo naledi","translated_title":"","metadata":{"abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.","publication_date":{"day":null,"month":null,"year":2016,"errors":{}},"publication_name":"The 85th Annual Meeting of the American Association of Physical Anthropologists, Atlanta, GA"},"translated_abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.","internal_url":"https://www.academia.edu/117067166/Thigh_and_leg_remains_of_Homo_naledi","translated_internal_url":"","created_at":"2024-04-04T06:35:02.125-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Thigh_and_leg_remains_of_Homo_naledi","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":54589,"name":"Anatomy","url":"https://www.academia.edu/Documents/in/Anatomy"},{"id":66145,"name":"Hominin evolution","url":"https://www.academia.edu/Documents/in/Hominin_evolution"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":366875,"name":"Fibulae","url":"https://www.academia.edu/Documents/in/Fibulae"},{"id":1146774,"name":"Thigh","url":"https://www.academia.edu/Documents/in/Thigh"},{"id":1737745,"name":"The Rising Star","url":"https://www.academia.edu/Documents/in/The_Rising_Star"},{"id":2104284,"name":"Homo naledi","url":"https://www.academia.edu/Documents/in/Homo_naledi"},{"id":2394726,"name":"Patella","url":"https://www.academia.edu/Documents/in/Patella"}],"urls":[{"id":40844198,"url":"https://meeting.physanth.org/program/2016/session39/marchi-2016-thigh-and-leg-remains-of-homo-naledi.html"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067165"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/117067165/Comparability_of_skeletal_fibulae_surfaces_generated_by_different_source_scanning_dual_energy_scp_CT_scp_scan_vs_high_resolution_laser_scanning_and_scp_3D_scp_geometric_morphometric_validation"><img alt="Research paper thumbnail of Comparability of skeletal fibulae surfaces generated by different source scanning (dual‐energy <scp>CT</scp> scan vs. high resolution laser scanning) and <scp>3D</scp> geometric morphometric validation" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/117067165/Comparability_of_skeletal_fibulae_surfaces_generated_by_different_source_scanning_dual_energy_scp_CT_scp_scan_vs_high_resolution_laser_scanning_and_scp_3D_scp_geometric_morphometric_validation">Comparability of skeletal fibulae surfaces generated by different source scanning (dual‐energy <scp>CT</scp> scan vs. high resolution laser scanning) and <scp>3D</scp> geometric morphometric validation</a></div><div class="wp-workCard_item"><span>Journal of Anatomy</span><span>, Jun 25, 2022</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067165"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067165"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067165; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067160"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur"><img alt="Research paper thumbnail of The locomotion of<i>Babakotia radofilai</i>inferred from epiphyseal and diaphyseal morphology of the humerus and femur" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur">The locomotion of<i>Babakotia radofilai</i>inferred from epiphyseal and diaphyseal morphology of the humerus and femur</a></div><div class="wp-workCard_item"><span>Journal of Morphology</span><span>, Jun 20, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Palaeopropithecids, or &amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Palaeopropithecids, or &amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. The most recently discovered genus of the palaeopropithecids is Babakotia, and it has been described as more arboreal than Mesopropithecus, but less than Palaeopropithecus. In this article, the within-bone and between-bones articular and cross-sectional diaphyseal proportions of the humerus and femur of Babakotia were compared to extant lemurs, Mesopropithecus and Palaeopropithecus in order to further understand its arboreal adaptations. Additionally, a sample of apes and sloths (Choloepus and Bradypus) are included as functional outgroups composed of suspensory adapted primates and non-primates. Results show that Babakotia and Mesopropithecus both have high humeral/femoral shaft strength proportions, similar to extant great apes and sloths and indicative of forelimb suspensory behavior, with Babakotia more extreme in this regard. All three subfossil taxa have relatively large femoral heads, also associated with suspension in modern taxa. However, Babakotia and Mesopropithecus (but not Palaeopropithecus) have relatively small femoral head surface area to shaft strength proportions suggesting that hind-limb positioning in these taxa during climbing and other behaviors was different than in extant great apes, involving less mobility. Knee and humeral articular dimensions relative to shaft strengths are small in Babakotia and Mesopropithecus, similar to those found in modern sloths and divergent from those in extant great apes and lemurs, suggesting more sloth-like use of these joints during locomotion. Mesopropithecus and Babakotia are more similar to Choloepus in humerofemoral head and length proportions while Palaeopropithecus is more similar to Bradypus. These results provide further evidence of the suspensory adaptations of Babakotia and further highlight similarities to both extant suspensory primates and non-primate slow arboreal climbers and hangers. J. Morphol., 2016. © 2016 Wiley Periodicals, Inc.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067160"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067160"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067160; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067160]").text(description); $(".js-view-count[data-work-id=117067160]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067160; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067160']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067160, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067160]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067160,"title":"The locomotion of\u003ci\u003eBabakotia radofilai\u003c/i\u003einferred from epiphyseal and diaphyseal morphology of the humerus and femur","translated_title":"","metadata":{"abstract":"Palaeopropithecids, or \u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,\u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. The most recently discovered genus of the palaeopropithecids is Babakotia, and it has been described as more arboreal than Mesopropithecus, but less than Palaeopropithecus. In this article, the within-bone and between-bones articular and cross-sectional diaphyseal proportions of the humerus and femur of Babakotia were compared to extant lemurs, Mesopropithecus and Palaeopropithecus in order to further understand its arboreal adaptations. Additionally, a sample of apes and sloths (Choloepus and Bradypus) are included as functional outgroups composed of suspensory adapted primates and non-primates. Results show that Babakotia and Mesopropithecus both have high humeral/femoral shaft strength proportions, similar to extant great apes and sloths and indicative of forelimb suspensory behavior, with Babakotia more extreme in this regard. All three subfossil taxa have relatively large femoral heads, also associated with suspension in modern taxa. However, Babakotia and Mesopropithecus (but not Palaeopropithecus) have relatively small femoral head surface area to shaft strength proportions suggesting that hind-limb positioning in these taxa during climbing and other behaviors was different than in extant great apes, involving less mobility. Knee and humeral articular dimensions relative to shaft strengths are small in Babakotia and Mesopropithecus, similar to those found in modern sloths and divergent from those in extant great apes and lemurs, suggesting more sloth-like use of these joints during locomotion. Mesopropithecus and Babakotia are more similar to Choloepus in humerofemoral head and length proportions while Palaeopropithecus is more similar to Bradypus. These results provide further evidence of the suspensory adaptations of Babakotia and further highlight similarities to both extant suspensory primates and non-primate slow arboreal climbers and hangers. J. Morphol., 2016. © 2016 Wiley Periodicals, Inc.","publisher":"Wiley","publication_date":{"day":20,"month":6,"year":2016,"errors":{}},"publication_name":"Journal of Morphology"},"translated_abstract":"Palaeopropithecids, or \u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,\u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. The most recently discovered genus of the palaeopropithecids is Babakotia, and it has been described as more arboreal than Mesopropithecus, but less than Palaeopropithecus. In this article, the within-bone and between-bones articular and cross-sectional diaphyseal proportions of the humerus and femur of Babakotia were compared to extant lemurs, Mesopropithecus and Palaeopropithecus in order to further understand its arboreal adaptations. Additionally, a sample of apes and sloths (Choloepus and Bradypus) are included as functional outgroups composed of suspensory adapted primates and non-primates. Results show that Babakotia and Mesopropithecus both have high humeral/femoral shaft strength proportions, similar to extant great apes and sloths and indicative of forelimb suspensory behavior, with Babakotia more extreme in this regard. All three subfossil taxa have relatively large femoral heads, also associated with suspension in modern taxa. However, Babakotia and Mesopropithecus (but not Palaeopropithecus) have relatively small femoral head surface area to shaft strength proportions suggesting that hind-limb positioning in these taxa during climbing and other behaviors was different than in extant great apes, involving less mobility. Knee and humeral articular dimensions relative to shaft strengths are small in Babakotia and Mesopropithecus, similar to those found in modern sloths and divergent from those in extant great apes and lemurs, suggesting more sloth-like use of these joints during locomotion. Mesopropithecus and Babakotia are more similar to Choloepus in humerofemoral head and length proportions while Palaeopropithecus is more similar to Bradypus. These results provide further evidence of the suspensory adaptations of Babakotia and further highlight similarities to both extant suspensory primates and non-primate slow arboreal climbers and hangers. J. Morphol., 2016. © 2016 Wiley Periodicals, Inc.","internal_url":"https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur","translated_internal_url":"","created_at":"2024-04-04T06:35:00.866-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":167,"name":"Physiology","url":"https://www.academia.edu/Documents/in/Physiology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9658,"name":"Locomotion","url":"https://www.academia.edu/Documents/in/Locomotion"},{"id":10866,"name":"Morphology","url":"https://www.academia.edu/Documents/in/Morphology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":54589,"name":"Anatomy","url":"https://www.academia.edu/Documents/in/Anatomy"},{"id":84915,"name":"Lemur","url":"https://www.academia.edu/Documents/in/Lemur"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":90326,"name":"Fossils","url":"https://www.academia.edu/Documents/in/Fossils"},{"id":360548,"name":"Humerus","url":"https://www.academia.edu/Documents/in/Humerus"},{"id":435540,"name":"Primate Locomotion","url":"https://www.academia.edu/Documents/in/Primate_Locomotion"},{"id":459525,"name":"Hylobates","url":"https://www.academia.edu/Documents/in/Hylobates"},{"id":484321,"name":"Sloths","url":"https://www.academia.edu/Documents/in/Sloths"},{"id":519447,"name":"Hominidae","url":"https://www.academia.edu/Documents/in/Hominidae"},{"id":683170,"name":"Sloth","url":"https://www.academia.edu/Documents/in/Sloth"},{"id":1034861,"name":"Epiphyses","url":"https://www.academia.edu/Documents/in/Epiphyses"},{"id":1299102,"name":"Arboreal Locomotion","url":"https://www.academia.edu/Documents/in/Arboreal_Locomotion"}],"urls":[{"id":40844192,"url":"https://doi.org/10.1002/jmor.20569"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067159"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067159/Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis"><img alt="Research paper thumbnail of Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis" class="work-thumbnail" src="https://attachments.academia-assets.com/113024804/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067159/Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis">Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis</a></div><div class="wp-workCard_item"><span>Journal of Human Evolution</span><span>, Aug 1, 2015</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="7e32d01e3e26469bbbe8ee7310f13c84" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":113024804,"asset_id":117067159,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/113024804/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067159"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067159"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067159; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067159]").text(description); $(".js-view-count[data-work-id=117067159]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067159; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067159']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067159, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "7e32d01e3e26469bbbe8ee7310f13c84" } } $('.js-work-strip[data-work-id=117067159]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067159,"title":"Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis","translated_title":"","metadata":{"publisher":"Elsevier BV","grobid_abstract":"The fibula has rarely been considered in anthropological studies. However differences in morphologyand inferred functionof the fibula between human and non-human apes have been noted in the past and related to differences in locomotor behavior. Recent studies have pointed out the correlation between diaphyseal rigidity of the fibula and tibia and locomotor behavior in living hominids, and its possible application for inferring early hominin locomotor behavior. The problem with the application of the method proposed in these studies is the extreme rarity of associated early hominin fibula and tibia. Additionally, previous studies investigating morphological traits of fibulotalar articular facets to infer the degree of arboreality in fossil australopiths were often qualitative. In the present study, articular measurements of the distal fibula of living great apes and humans (Pongo, Gorilla, Pan and Homo) are quantified and compared to Australopithecus afarensis distal fibulae. Quantitative analysis is carried out for articular areas and breadths of the fibulotalar articular facets, of the angles formed by the fibulotalar articular facets and the longitudinal axis of the fibula, and of the angle between the proximal fibulotalar articular facet and the subcutaneous triangular area. Results show that the fibula of Au. afarensis bears some traits consistent with modern terrestrial bipedalism, like a more laterally facing lateral malleolus, in association with more ape-like traits, like the smaller distal fibulotalar articular facet area and the more inferiorly oriented fibulotalar articular facets, consistent with Au. afarensis being a terrestrial hominin adapted for some form of arboreality.","publication_date":{"day":1,"month":8,"year":2015,"errors":{}},"publication_name":"Journal of Human 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hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis"><img alt="Research paper thumbnail of Nature and relationships of Sahelanthropus tchadensis" class="work-thumbnail" src="https://attachments.academia-assets.com/113024834/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis">Nature and relationships of Sahelanthropus tchadensis</a></div><div class="wp-workCard_item"><span>Journal of Human Evolution</span><span>, Dec 1, 2020</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="265bdfdb2a5f927df43b8ec9e5b0bbb7" 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Sahelanthropus tchadensis","grobid_abstract":"A partial left femur (TM 266-01-063) was recovered in July 2001 at Toros-Menalla, Chad, at the same fossiliferous location as the late Miocene holotype of Sahelanthropus tchadensis (the cranium TM 266-01-060-1). It was recognized as a probable primate femur in 2004 when one of the authors was undertaking a taphonomic survey of the fossil assemblages from Toros-Menalla. We are confident the TM 266 femoral shaft belongs to a hominid. It could sample a hominid hitherto unrepresented at Toros-Menalla, but a more parsimonious working hypothesis is that it belongs to S. tchadensis. The differences between TM 266 and the late Miocene Orrorin tugenensis partial femur BAR 1002 0 00, from Kenya, are consistent with maintaining at least a species-level distinction between S. tchadensis and O. tugenensis. The results of our preliminary functional analysis suggest the TM 266 femoral shaft belongs to an individual that was not habitually bipedal, something that should be taken into account when considering the relationships of S. tchadensis. The circumstances of its discovery should encourage researchers to check to see whether there is more postcranial evidence of S. tchadensis among the fossils recovered from Toros-Menalla.","publication_date":{"day":1,"month":12,"year":2020,"errors":{}},"publication_name":"Journal of Human Evolution","grobid_abstract_attachment_id":113024834},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis","translated_internal_url":"","created_at":"2024-04-04T06:35:00.481-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024834,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024834/thumbnails/1.jpg","file_name":"j.jhevol.2020.10289820240404-1-ti8u8p.pdf","download_url":"https://www.academia.edu/attachments/113024834/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Nature_and_relationships_of_Sahelanthrop.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024834/j.jhevol.2020.10289820240404-1-ti8u8p-libre.pdf?1712240485=\u0026response-content-disposition=attachment%3B+filename%3DNature_and_relationships_of_Sahelanthrop.pdf\u0026Expires=1733264551\u0026Signature=CfMB4xHO4AvV6vhhXfCiXMw7cHF~c4pIG67Wtv-YV1k35JtmxcZDhfy41DAbCZZw5E~8CGGcCJSY~wqPXjfdIJ0rxltb0mc12vbIuW-P4~exerN68QW2bLuwDOLms8mCuE9GF5cY2P0uHD0m~dk07IhmNJ8IXcKSDvv0elzq6KR4RdvHf0Ap22l3CNLInTvptrVr2NiKBJU4ZxLj2VkDZJB~H~QUHzwbXHpEHnScRuJ~HgNKj0T1qm66~ko9Iqw-xXzRfXLTLTsoDcDbCGeSrEeEtVDnr~wzbu~uIMayVWJEMnF5g7cw21jkMarfmcYUEiPZKqV~RAueTrz37FI9GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Nature_and_relationships_of_Sahelanthropus_tchadensis","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":113024834,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024834/thumbnails/1.jpg","file_name":"j.jhevol.2020.10289820240404-1-ti8u8p.pdf","download_url":"https://www.academia.edu/attachments/113024834/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Nature_and_relationships_of_Sahelanthrop.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024834/j.jhevol.2020.10289820240404-1-ti8u8p-libre.pdf?1712240485=\u0026response-content-disposition=attachment%3B+filename%3DNature_and_relationships_of_Sahelanthrop.pdf\u0026Expires=1733264551\u0026Signature=CfMB4xHO4AvV6vhhXfCiXMw7cHF~c4pIG67Wtv-YV1k35JtmxcZDhfy41DAbCZZw5E~8CGGcCJSY~wqPXjfdIJ0rxltb0mc12vbIuW-P4~exerN68QW2bLuwDOLms8mCuE9GF5cY2P0uHD0m~dk07IhmNJ8IXcKSDvv0elzq6KR4RdvHf0Ap22l3CNLInTvptrVr2NiKBJU4ZxLj2VkDZJB~H~QUHzwbXHpEHnScRuJ~HgNKj0T1qm66~ko9Iqw-xXzRfXLTLTsoDcDbCGeSrEeEtVDnr~wzbu~uIMayVWJEMnF5g7cw21jkMarfmcYUEiPZKqV~RAueTrz37FI9GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":261,"name":"Geography","url":"https://www.academia.edu/Documents/in/Geography"},{"id":392,"name":"Archaeology","url":"https://www.academia.edu/Documents/in/Archaeology"},{"id":767,"name":"Anthropology","url":"https://www.academia.edu/Documents/in/Anthropology"},{"id":772,"name":"Human Evolution","url":"https://www.academia.edu/Documents/in/Human_Evolution"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":66145,"name":"Hominin evolution","url":"https://www.academia.edu/Documents/in/Hominin_evolution"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":530866,"name":"Hominid Evolution","url":"https://www.academia.edu/Documents/in/Hominid_Evolution"},{"id":1131312,"name":"Academic","url":"https://www.academia.edu/Documents/in/Academic"}],"urls":[{"id":40844190,"url":"https://www.sciencedirect.com/science/article/am/pii/S0047248420301597"}]}, dispatcherData: dispatcherData }); 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Differences in locomotor behavior among the great apes (knuckle-walking vs. quadrumanous climbing) can produce biomechanical differences that may be elucidated by the parallel study of cross-sectional characteristics of metacarpals and metatarsals. The aim of this work is to study the cross-sectional geometric properties of these bones and their correlation with locomotor behavior in large-bodied hominoids. The comparisons between bending moments of metacarpals and metatarsals of the same ray furnished interesting results. Metacarpals III and especially IV of the knuckle-walking African apes were relatively stronger than those of humans and orangutans, and metatarsal V of humans was relatively stronger than those of the great apes. Interestingly, the relative robusticity of the metacarpal IV of the quadrumanous orangutan was between that of the African apes and that of humans. The main conclusions of the study are: 1) cross-sectional dimensions of metacarpals and metatarsals are influenced by locomotor modes in great apes and humans; 2) interlimb comparisons of cross-sectional properties of metacarpals and metatarsals are good indicators of locomotor modes in great apes and humans; and 3) the results of this study are in accord with those of previous analyses of plantar pressure and morphofunctional traits of the same bones, and with behavioral studies. These results provide a data base from which it will be possible to compare the morphology of the fossils in order to gain insight into the locomotor repertoires of extinct taxa.","publication_date":{"day":1,"month":12,"year":2005,"errors":{}},"publication_name":"Journal of Human Evolution","grobid_abstract_attachment_id":113024839},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067156/The_cross_sectional_geometry_of_the_hand_and_foot_bones_of_the_Hominoidea_and_its_relationship_to_locomotor_behavior","translated_internal_url":"","created_at":"2024-04-04T06:35:00.076-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024839,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024839/thumbnails/1.jpg","file_name":"j.jhevol.2005.08.00220240404-1-xcl7e7.pdf","download_url":"https://www.academia.edu/attachments/113024839/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"The_cross_sectional_geometry_of_the_hand.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024839/j.jhevol.2005.08.00220240404-1-xcl7e7-libre.pdf?1712240476=\u0026response-content-disposition=attachment%3B+filename%3DThe_cross_sectional_geometry_of_the_hand.pdf\u0026Expires=1733264551\u0026Signature=azt7lD3NvcMsUILvatUXNaYSLzxwo-5IkbF1femjUjiksAIFcgWEFsqTt2SjPQx1daLeAzhHl~~6TZDKct2kiUrI6EDHXEV5ZYoVZ0ZLpPNffZQG2ws402D7bg-XMO78MFL8xhcXiO5RdL0xLtHGAuvAJh9Gu2UgiNMbT5mB2mHnNwIjlsKc355rPGUNja97oF3cR1kNNgCeoU55gzXO6Q~yK6npVsR2cvmiBant0Skw9sy6P81KUizRw5b-AFYLmSAtVC0SD53WA4RvL5wHlR6oK8sooXkBNO83reFWBDbxSqFo3BbYHDbiH7cuH9KggYU~EI-Iun3eNyvdei42fw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"The_cross_sectional_geometry_of_the_hand_and_foot_bones_of_the_Hominoidea_and_its_relationship_to_locomotor_behavior","translated_slug":"","page_count":19,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano 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class="js-work-strip profile--work_container" data-work-id="117067155"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso"><img alt="Research paper thumbnail of The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso" class="work-thumbnail" src="https://attachments.academia-assets.com/113024836/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso">The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso</a></div><div class="wp-workCard_item"><span>Homo-journal of Comparative Human Biology</span><span>, 2002</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="36641da1409a839f8832de401680104c" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":113024836,"asset_id":117067155,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067155"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa 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$('.js-work-strip[data-work-id=117067155]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067155,"title":"The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso","translated_title":"","metadata":{"publisher":"Elsevier BV","ai_title_tag":"Skeletal Analysis of Magna Graecia Necropoles: Timmari \u0026 Montescaglioso","grobid_abstract":"The aim of this work is to outline a general picture of life style and conditions of a population living in Magna Graecia between the 7th and the 4th c. BC by the study of human skeletal remains found in two necropoles from the Matera province, Timmari and Montescaglioso, neighbouring Metaponto, one of the main Ionian Greek colonies. The biological reconstruction was attempted by a holistic approach which foresees the use of anthropometric, anthroposcopic, palaeodemographic, palaeopathological data, the study of skeletal and dentoalveolar indicators of environmental stress and the integration with archaeological and historical information. Interpretation of the results was also based on comparisons with coeval sites from Central-Southern Italy, from Greece and with earlier and later sites from the same region. The two samples from Matera did not show appreciable differences with the other Southern Italian coeval series when compared on the basis of metric and morphometric traits. The comparison with Greek samples was hampered by the scarcity of pertinent data. A high level of muscular activity was observed in males and females, with males clearly more mobile than females. Sexual dimorphism and limb bone lateralisation were marked. Health conditions and nutritional status were good. Riassunto Lo scopo di questo lavoro è delineare un quadro generale dello stile di vita e delle condizioni generali della popolazione che viveva nella Magna Grecia nei secoli compresi tra il 7 th e il 4 th a.C. Allo scopo sono stati studiati i resti scheletrici umani provenienti da due necropoli situate in provincia di Matera, Timmari e Montescaglioso, vicino a Metaponto che è stata una delle più importanti colonie greche sullo Ionio. La ricostruzione biologica delle due popolazioni è stata effettuata mediante un approccio olistico che comprende il rilevamento dai dati antropometrici, antroposcopici, paleodemografici e paleopatologici insieme allo studio degli indicatori scheletrici e dentoalveolari di stress ambientale, il tutto integrato con informazioni di carattere storico e archeologico. I risultati di queste analisi sono inoltre stati messi a confronto con campioni scheletrici provenienti da siti coevi dell'Italia centrale e meridionale, dalla Grecia e dalla stessa regione ma antecedenti (neolitici) e posteriori (medievali). Sulla base dei caratteri metrici e morfometrici, i due campioni qui analizzati (Timmari e Montescaglioso Belvedere) non hanno mostrato differenze apprezzabili rispetto alle altre serie coeve provenienti dall'Italia meridionale. Il confronto con le serie provenienti da necropoli greche è stato reso difficile dalla scarsità di dati relativi. E' stato rilevato un alto grado di attività muscolare sia nei maschi sia nelle femmine, con i maschi che mostrano chiari segni di maggiore mobilità. Il dimorfismo sessuale e il grado di lateralizzazione degli arti è risultato marcato. In generale, i campioni qui analizzati sono risultati in buone condizioni nutrizionali e di salute.","publication_date":{"day":null,"month":null,"year":2002,"errors":{}},"publication_name":"Homo-journal of Comparative Human Biology","grobid_abstract_attachment_id":113024836},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso","translated_internal_url":"","created_at":"2024-04-04T06:34:59.881-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024836,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024836/thumbnails/1.jpg","file_name":"0018-442x-0003820240404-1-7tru40.pdf","download_url":"https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"The_skeletal_biology_of_two_Italian_peni.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024836/0018-442x-0003820240404-1-7tru40-libre.pdf?1712240479=\u0026response-content-disposition=attachment%3B+filename%3DThe_skeletal_biology_of_two_Italian_peni.pdf\u0026Expires=1733036086\u0026Signature=MAD9HWdqgjJzmIGFPsh-eDrBQePCZwNWaLLnLNZdic3BDV5RiFTzHhj~c70S~5vo9B4m5Y5~WyVUl7JB4OetEBvfSvf3ZBkMhgdCkKSkuhMMLnjFDhoafvQ7k~vjGrU2YN1WiIS~X8tw6ShLtxT3uaEinN6LCabbRvkXFgUlSasCynxN3TlZ3rozsV~LmyixBrzWV-leXLCd9W2rjbJ013PWQntQd6e~GVmL-y7yh14iHIyfod549GQPIwJOST-rZXF8m9RRwl0~X3nARfRRlpwJHUmeomkO2cdks5Ayg1CN5c6BO3CDwH0teehfvbnRHfZxRiy63CWJiv~T78NA9Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso","translated_slug":"","page_count":20,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":113024836,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024836/thumbnails/1.jpg","file_name":"0018-442x-0003820240404-1-7tru40.pdf","download_url":"https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"The_skeletal_biology_of_two_Italian_peni.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024836/0018-442x-0003820240404-1-7tru40-libre.pdf?1712240479=\u0026response-content-disposition=attachment%3B+filename%3DThe_skeletal_biology_of_two_Italian_peni.pdf\u0026Expires=1733036086\u0026Signature=MAD9HWdqgjJzmIGFPsh-eDrBQePCZwNWaLLnLNZdic3BDV5RiFTzHhj~c70S~5vo9B4m5Y5~WyVUl7JB4OetEBvfSvf3ZBkMhgdCkKSkuhMMLnjFDhoafvQ7k~vjGrU2YN1WiIS~X8tw6ShLtxT3uaEinN6LCabbRvkXFgUlSasCynxN3TlZ3rozsV~LmyixBrzWV-leXLCd9W2rjbJ013PWQntQd6e~GVmL-y7yh14iHIyfod549GQPIwJOST-rZXF8m9RRwl0~X3nARfRRlpwJHUmeomkO2cdks5Ayg1CN5c6BO3CDwH0teehfvbnRHfZxRiy63CWJiv~T78NA9Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":310,"name":"Demography","url":"https://www.academia.edu/Documents/in/Demography"},{"id":1704,"name":"Bioarchaeology","url":"https://www.academia.edu/Documents/in/Bioarchaeology"},{"id":5018,"name":"Anthropometry","url":"https://www.academia.edu/Documents/in/Anthropometry"},{"id":7471,"name":"Life Style","url":"https://www.academia.edu/Documents/in/Life_Style"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":30181,"name":"Gender Identity","url":"https://www.academia.edu/Documents/in/Gender_Identity"},{"id":44744,"name":"Sexual dimorphism","url":"https://www.academia.edu/Documents/in/Sexual_dimorphism"},{"id":45213,"name":"Italy","url":"https://www.academia.edu/Documents/in/Italy"},{"id":85909,"name":"Iron Age Italy","url":"https://www.academia.edu/Documents/in/Iron_Age_Italy"},{"id":90326,"name":"Fossils","url":"https://www.academia.edu/Documents/in/Fossils"},{"id":192551,"name":"Nutritional Status","url":"https://www.academia.edu/Documents/in/Nutritional_Status"},{"id":232534,"name":"Health Status","url":"https://www.academia.edu/Documents/in/Health_Status"},{"id":413192,"name":"Sex Factors","url":"https://www.academia.edu/Documents/in/Sex_Factors"},{"id":1208706,"name":"Environment","url":"https://www.academia.edu/Documents/in/Environment"},{"id":1256683,"name":"Bone and Bones","url":"https://www.academia.edu/Documents/in/Bone_and_Bones"},{"id":2677637,"name":"Sex Characteristics","url":"https://www.academia.edu/Documents/in/Sex_Characteristics"}],"urls":[{"id":40844187,"url":"https://doi.org/10.1078/0018-442x-00038"}]}, dispatcherData: dispatcherData }); 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Genetic evidence suggests that the lineages leading to these taxa began diverging from one another between approximately 1 and 3 million years ago. Thus, gorillas offer a special opportunity to examine the degree to which morphology of recently diverged taxa may be \"fine-tuned\" to differing ecological requirements. Using three-dimensional (3D) geometric morphometrics, we compared talar morphology in a sample of 87 specimens including western (lowland), mountain (highland), and grauer gorillas (lowland and highland populations). Talar shape was captured with a series of landmarks and semilandmarks superimposed by generalized Procrustes analysis. A between-group principal components analysis of overall talar shape separates gorillas by ecological habitat and by taxon. An analysis of only the trochlea and lateral malleolar facet identifies subtle variations in trochlear shape between western lowland and lowland grauer gorillas, potentially indicative of convergent evolution of arboreal adaptations in the talus. Lastly, talar shape scales differently with centroid size for highland and lowland gorillas, suggesting that ankle morphology may track bodysize mediated variation in arboreal behaviors differently depending on ecological setting. Several of the observed shape differences are linked biomechanically to the facilitation of climbing in lowland gorillas and to stability and load-bearing on terrestrial substrates in the highland taxa, providing an important comparative model for studying morphological variation in groups known only from fossils (e.g., early hominins).","publication_date":{"day":1,"month":7,"year":2019,"errors":{}},"publication_name":"Journal of Human 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href="https://www.academia.edu/117067153/Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale"><img alt="Research paper thumbnail of Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/117067153/Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale">Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. 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Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. 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href="https://www.academia.edu/117067149/Cross_sectional_geometry_of_the_humerus_of_a_Western_Liguria_Neolithic_sample"><img alt="Research paper thumbnail of Cross-sectional geometry of the humerus of a Western Liguria Neolithic sample" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/117067149/Cross_sectional_geometry_of_the_humerus_of_a_Western_Liguria_Neolithic_sample">Cross-sectional geometry of the humerus of a Western Liguria Neolithic sample</a></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span 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_.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067149]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067149,"title":"Cross-sectional geometry of the humerus of a Western Liguria Neolithic 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data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/117067148/Relative_robusticity_of_the_Homo_floresiensis_tibia_and_fibula">Relative robusticity of the Homo floresiensis tibia and fibula</a></div><div class="wp-workCard_item"><span>American Journal of Physical Anthropology</span><span>, 2011</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this spec...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this species retained primitive characteristics of body shape and interlimb proportions, the H. floresiensis fibula remains an unexamined part of the equation. The leg of modern humans reflects our status as habitual bipeds and is signaled by a gracile fibula relative to a more robust, weight-bearing tibia. This study investigated whether LB1, the type specimen of H. floresiensis, possesses a robust fibula or displays the gracile fibula that is the signature of our species. CT scans of the fibula and tibia of LB1 and a sample of small-bodied modern humans (N=10) were used to analyze cross-sectional geometric (CSG) properties (e.g., cortical area and polar section modulus, Zp) of the tibia and fibula at midshaft. These new data were added to the much larger sample published by Marchi (2007), which included modern humans, chimpanzees, gorillas, orangutans and gibbons. External contours of additional fossils of the genus Homo (e.g., OH 35, KNM-WT-15000) were also examined in order to evaluate when the modern condition arose during the course of human evolution. Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. This work was supported by grants from the Wenner-Gren Foundation, the Leakey Foundation, the National Geographic Society, and the Australian Research Council.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067148"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067148"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067148; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067148]").text(description); $(".js-view-count[data-work-id=117067148]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067148; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067148']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067148, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067148]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067148,"title":"Relative robusticity of the Homo floresiensis tibia and fibula","translated_title":"","metadata":{"abstract":"ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this species retained primitive characteristics of body shape and interlimb proportions, the H. floresiensis fibula remains an unexamined part of the equation. The leg of modern humans reflects our status as habitual bipeds and is signaled by a gracile fibula relative to a more robust, weight-bearing tibia. This study investigated whether LB1, the type specimen of H. floresiensis, possesses a robust fibula or displays the gracile fibula that is the signature of our species. CT scans of the fibula and tibia of LB1 and a sample of small-bodied modern humans (N=10) were used to analyze cross-sectional geometric (CSG) properties (e.g., cortical area and polar section modulus, Zp) of the tibia and fibula at midshaft. These new data were added to the much larger sample published by Marchi (2007), which included modern humans, chimpanzees, gorillas, orangutans and gibbons. External contours of additional fossils of the genus Homo (e.g., OH 35, KNM-WT-15000) were also examined in order to evaluate when the modern condition arose during the course of human evolution. Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. This work was supported by grants from the Wenner-Gren Foundation, the Leakey Foundation, the National Geographic Society, and the Australian Research Council.","publisher":"Wiley","publication_date":{"day":null,"month":null,"year":2011,"errors":{}},"publication_name":"American Journal of Physical Anthropology"},"translated_abstract":"ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this species retained primitive characteristics of body shape and interlimb proportions, the H. floresiensis fibula remains an unexamined part of the equation. The leg of modern humans reflects our status as habitual bipeds and is signaled by a gracile fibula relative to a more robust, weight-bearing tibia. This study investigated whether LB1, the type specimen of H. floresiensis, possesses a robust fibula or displays the gracile fibula that is the signature of our species. CT scans of the fibula and tibia of LB1 and a sample of small-bodied modern humans (N=10) were used to analyze cross-sectional geometric (CSG) properties (e.g., cortical area and polar section modulus, Zp) of the tibia and fibula at midshaft. These new data were added to the much larger sample published by Marchi (2007), which included modern humans, chimpanzees, gorillas, orangutans and gibbons. External contours of additional fossils of the genus Homo (e.g., OH 35, KNM-WT-15000) were also examined in order to evaluate when the modern condition arose during the course of human evolution. Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. This work was supported by grants from the Wenner-Gren Foundation, the Leakey Foundation, the National Geographic Society, and the Australian Research Council.","internal_url":"https://www.academia.edu/117067148/Relative_robusticity_of_the_Homo_floresiensis_tibia_and_fibula","translated_internal_url":"","created_at":"2024-04-04T06:34:58.597-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Relative_robusticity_of_the_Homo_floresiensis_tibia_and_fibula","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9658,"name":"Locomotion","url":"https://www.academia.edu/Documents/in/Locomotion"},{"id":42996,"name":"American Journal of Physical Anthropology","url":"https://www.academia.edu/Documents/in/American_Journal_of_Physical_Anthropology"},{"id":71579,"name":"Cross-Sectional Geometry","url":"https://www.academia.edu/Documents/in/Cross-Sectional_Geometry"},{"id":85893,"name":"Fibula","url":"https://www.academia.edu/Documents/in/Fibula"},{"id":219868,"name":"Tibia Fibula Biomechanics","url":"https://www.academia.edu/Documents/in/Tibia_Fibula_Biomechanics"}],"urls":[{"id":40844180,"url":"https://arpi.unipi.it/handle/11568/146256"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="13044" id="papers"><div class="js-work-strip profile--work_container" data-work-id="117067167"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_"><img alt="Research paper thumbnail of The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_">The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)</a></div><div class="wp-workCard_item"><span>American journal of biological anthropology</span><span>, Nov 16, 2021</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ObjectivesLong bone variations during growth are susceptible to the combined action of nutritiona...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067167"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067167"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067167; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067167]").text(description); $(".js-view-count[data-work-id=117067167]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067167; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067167']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067167, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067167]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067167,"title":"The relationship between bipedalism and growth: A metric assessment in a documented modern skeletal collection (Certosa Collection, Bologna, Italy)","translated_title":"","metadata":{"abstract":"ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.","publisher":"Wiley","publication_date":{"day":16,"month":11,"year":2021,"errors":{}},"publication_name":"American journal of biological anthropology"},"translated_abstract":"ObjectivesLong bone variations during growth are susceptible to the combined action of nutritional, hormonal, and genetic factors that may modulate the mechanical forces acting upon growing individuals as they progressively acquire a mature gait. In this work, we explore diaphyseal length and breadth variations of tibia and fibula during ontogeny (a) to test the presence of changes in relation to early toddling, and (b) to further our understanding of developmental patterns in relation to sex.Materials and MethodsLengths, breadths, and indices were analyzed on right and left leg bones of 68 subadult individuals (Human Identified Skeletal Collection of the University of Bologna, Italy). Analyses included intersex and age classes (1, 0–1 year; 2, 1.1–3 years; 3, 3.1–6 years) comparisons, linear regressions with age and assessment of correlation among tibial and fibular measurements, as well as principal component analysis.ResultsA significant difference emerged among age class 1 and the others. Age class 1 and 3 differ between them, while age class 2 overlaps with the others. No sex dimorphism was detected. All measurements were strongly correlated with age. Tibial and fibular measurements correlated with each other.ConclusionsOur results relate the progressive emergence of toddling attempts in growing individuals at the end of the first year of age. No significant sex differences were found, suggesting that tibial and fibula growth might diverge between sexes in later childhood. We provide quantitative data regarding tibial and fibular linear growth and its timing in a modern documented osteological sample from Italy.","internal_url":"https://www.academia.edu/117067167/The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_","translated_internal_url":"","created_at":"2024-04-04T06:35:02.337-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"The_relationship_between_bipedalism_and_growth_A_metric_assessment_in_a_documented_modern_skeletal_collection_Certosa_Collection_Bologna_Italy_","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9047,"name":"Osteology","url":"https://www.academia.edu/Documents/in/Osteology"},{"id":44744,"name":"Sexual dimorphism","url":"https://www.academia.edu/Documents/in/Sexual_dimorphism"},{"id":85893,"name":"Fibula","url":"https://www.academia.edu/Documents/in/Fibula"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":168987,"name":"Bipedalism","url":"https://www.academia.edu/Documents/in/Bipedalism"}],"urls":[{"id":40844199,"url":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ajpa.24440"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067166"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067166/Thigh_and_leg_remains_of_Homo_naledi"><img alt="Research paper thumbnail of Thigh and leg remains of Homo naledi" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067166/Thigh_and_leg_remains_of_Homo_naledi">Thigh and leg remains of Homo naledi</a></div><div class="wp-workCard_item"><span>The 85th Annual Meeting of the American Association of Physical Anthropologists, Atlanta, GA</span><span>, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in So...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067166"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067166"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067166; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067166]").text(description); $(".js-view-count[data-work-id=117067166]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067166; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067166']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067166, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067166]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067166,"title":"Thigh and leg remains of Homo naledi","translated_title":"","metadata":{"abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.","publication_date":{"day":null,"month":null,"year":2016,"errors":{}},"publication_name":"The 85th Annual Meeting of the American Association of Physical Anthropologists, Atlanta, GA"},"translated_abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20 out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly, running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067160"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur"><img alt="Research paper thumbnail of The locomotion of<i>Babakotia radofilai</i>inferred from epiphyseal and diaphyseal morphology of the humerus and femur" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur">The locomotion of<i>Babakotia radofilai</i>inferred from epiphyseal and diaphyseal morphology of the humerus and femur</a></div><div class="wp-workCard_item"><span>Journal of Morphology</span><span>, Jun 20, 2016</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Palaeopropithecids, or &amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Palaeopropithecids, or &amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. The most recently discovered genus of the palaeopropithecids is Babakotia, and it has been described as more arboreal than Mesopropithecus, but less than Palaeopropithecus. In this article, the within-bone and between-bones articular and cross-sectional diaphyseal proportions of the humerus and femur of Babakotia were compared to extant lemurs, Mesopropithecus and Palaeopropithecus in order to further understand its arboreal adaptations. Additionally, a sample of apes and sloths (Choloepus and Bradypus) are included as functional outgroups composed of suspensory adapted primates and non-primates. Results show that Babakotia and Mesopropithecus both have high humeral/femoral shaft strength proportions, similar to extant great apes and sloths and indicative of forelimb suspensory behavior, with Babakotia more extreme in this regard. All three subfossil taxa have relatively large femoral heads, also associated with suspension in modern taxa. However, Babakotia and Mesopropithecus (but not Palaeopropithecus) have relatively small femoral head surface area to shaft strength proportions suggesting that hind-limb positioning in these taxa during climbing and other behaviors was different than in extant great apes, involving less mobility. Knee and humeral articular dimensions relative to shaft strengths are small in Babakotia and Mesopropithecus, similar to those found in modern sloths and divergent from those in extant great apes and lemurs, suggesting more sloth-like use of these joints during locomotion. Mesopropithecus and Babakotia are more similar to Choloepus in humerofemoral head and length proportions while Palaeopropithecus is more similar to Bradypus. These results provide further evidence of the suspensory adaptations of Babakotia and further highlight similarities to both extant suspensory primates and non-primate slow arboreal climbers and hangers. J. Morphol., 2016. © 2016 Wiley Periodicals, Inc.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067160"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067160"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067160; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067160]").text(description); $(".js-view-count[data-work-id=117067160]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067160; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067160']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067160, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067160]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067160,"title":"The locomotion of\u003ci\u003eBabakotia radofilai\u003c/i\u003einferred from epiphyseal and diaphyseal morphology of the humerus and femur","translated_title":"","metadata":{"abstract":"Palaeopropithecids, or \u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,\u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. 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Morphol., 2016. © 2016 Wiley Periodicals, Inc.","publisher":"Wiley","publication_date":{"day":20,"month":6,"year":2016,"errors":{}},"publication_name":"Journal of Morphology"},"translated_abstract":"Palaeopropithecids, or \u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot;sloth lemurs,\u0026amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;quot; are a diverse clade of large-bodied Malagasy subfossil primates characterized by their inferred suspensory positional behavior. The most recently discovered genus of the palaeopropithecids is Babakotia, and it has been described as more arboreal than Mesopropithecus, but less than Palaeopropithecus. In this article, the within-bone and between-bones articular and cross-sectional diaphyseal proportions of the humerus and femur of Babakotia were compared to extant lemurs, Mesopropithecus and Palaeopropithecus in order to further understand its arboreal adaptations. Additionally, a sample of apes and sloths (Choloepus and Bradypus) are included as functional outgroups composed of suspensory adapted primates and non-primates. Results show that Babakotia and Mesopropithecus both have high humeral/femoral shaft strength proportions, similar to extant great apes and sloths and indicative of forelimb suspensory behavior, with Babakotia more extreme in this regard. All three subfossil taxa have relatively large femoral heads, also associated with suspension in modern taxa. However, Babakotia and Mesopropithecus (but not Palaeopropithecus) have relatively small femoral head surface area to shaft strength proportions suggesting that hind-limb positioning in these taxa during climbing and other behaviors was different than in extant great apes, involving less mobility. Knee and humeral articular dimensions relative to shaft strengths are small in Babakotia and Mesopropithecus, similar to those found in modern sloths and divergent from those in extant great apes and lemurs, suggesting more sloth-like use of these joints during locomotion. Mesopropithecus and Babakotia are more similar to Choloepus in humerofemoral head and length proportions while Palaeopropithecus is more similar to Bradypus. These results provide further evidence of the suspensory adaptations of Babakotia and further highlight similarities to both extant suspensory primates and non-primate slow arboreal climbers and hangers. J. Morphol., 2016. © 2016 Wiley Periodicals, Inc.","internal_url":"https://www.academia.edu/117067160/The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur","translated_internal_url":"","created_at":"2024-04-04T06:35:00.866-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"The_locomotion_of_i_Babakotia_radofilai_i_inferred_from_epiphyseal_and_diaphyseal_morphology_of_the_humerus_and_femur","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":167,"name":"Physiology","url":"https://www.academia.edu/Documents/in/Physiology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9658,"name":"Locomotion","url":"https://www.academia.edu/Documents/in/Locomotion"},{"id":10866,"name":"Morphology","url":"https://www.academia.edu/Documents/in/Morphology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":54589,"name":"Anatomy","url":"https://www.academia.edu/Documents/in/Anatomy"},{"id":84915,"name":"Lemur","url":"https://www.academia.edu/Documents/in/Lemur"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":90326,"name":"Fossils","url":"https://www.academia.edu/Documents/in/Fossils"},{"id":360548,"name":"Humerus","url":"https://www.academia.edu/Documents/in/Humerus"},{"id":435540,"name":"Primate Locomotion","url":"https://www.academia.edu/Documents/in/Primate_Locomotion"},{"id":459525,"name":"Hylobates","url":"https://www.academia.edu/Documents/in/Hylobates"},{"id":484321,"name":"Sloths","url":"https://www.academia.edu/Documents/in/Sloths"},{"id":519447,"name":"Hominidae","url":"https://www.academia.edu/Documents/in/Hominidae"},{"id":683170,"name":"Sloth","url":"https://www.academia.edu/Documents/in/Sloth"},{"id":1034861,"name":"Epiphyses","url":"https://www.academia.edu/Documents/in/Epiphyses"},{"id":1299102,"name":"Arboreal Locomotion","url":"https://www.academia.edu/Documents/in/Arboreal_Locomotion"}],"urls":[{"id":40844192,"url":"https://doi.org/10.1002/jmor.20569"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067159"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067159/Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis"><img alt="Research paper thumbnail of Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis" class="work-thumbnail" src="https://attachments.academia-assets.com/113024804/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067159/Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis">Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis</a></div><div class="wp-workCard_item"><span>Journal of Human Evolution</span><span>, Aug 1, 2015</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="7e32d01e3e26469bbbe8ee7310f13c84" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":113024804,"asset_id":117067159,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/113024804/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067159"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067159"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067159; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067159]").text(description); $(".js-view-count[data-work-id=117067159]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067159; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067159']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067159, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "7e32d01e3e26469bbbe8ee7310f13c84" } } $('.js-work-strip[data-work-id=117067159]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067159,"title":"Using the morphology of the hominoid distal fibula to interpret arboreality in Australopithecus afarensis","translated_title":"","metadata":{"publisher":"Elsevier BV","grobid_abstract":"The fibula has rarely been considered in anthropological studies. However differences in morphologyand inferred functionof the fibula between human and non-human apes have been noted in the past and related to differences in locomotor behavior. Recent studies have pointed out the correlation between diaphyseal rigidity of the fibula and tibia and locomotor behavior in living hominids, and its possible application for inferring early hominin locomotor behavior. The problem with the application of the method proposed in these studies is the extreme rarity of associated early hominin fibula and tibia. Additionally, previous studies investigating morphological traits of fibulotalar articular facets to infer the degree of arboreality in fossil australopiths were often qualitative. In the present study, articular measurements of the distal fibula of living great apes and humans (Pongo, Gorilla, Pan and Homo) are quantified and compared to Australopithecus afarensis distal fibulae. Quantitative analysis is carried out for articular areas and breadths of the fibulotalar articular facets, of the angles formed by the fibulotalar articular facets and the longitudinal axis of the fibula, and of the angle between the proximal fibulotalar articular facet and the subcutaneous triangular area. Results show that the fibula of Au. afarensis bears some traits consistent with modern terrestrial bipedalism, like a more laterally facing lateral malleolus, in association with more ape-like traits, like the smaller distal fibulotalar articular facet area and the more inferiorly oriented fibulotalar articular facets, consistent with Au. afarensis being a terrestrial hominin adapted for some form of arboreality.","publication_date":{"day":1,"month":8,"year":2015,"errors":{}},"publication_name":"Journal of Human Evolution","grobid_abstract_attachment_id":113024804},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067159/Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis","translated_internal_url":"","created_at":"2024-04-04T06:35:00.672-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024804,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024804/thumbnails/1.jpg","file_name":"Marchi__2015__JHE__Post-Print.pdf","download_url":"https://www.academia.edu/attachments/113024804/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Using_the_morphology_of_the_hominoid_dis.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024804/Marchi__2015__JHE__Post-Print-libre.pdf?1712240504=\u0026response-content-disposition=attachment%3B+filename%3DUsing_the_morphology_of_the_hominoid_dis.pdf\u0026Expires=1733229915\u0026Signature=V4NVT5TS9uchAAQGYqiGK6joumHv4ZuqeOIbosOGmyjng3JWh1BeoiAotGN6pFrfbaBuuSmJ~tLmu-Zq4nRtC74tQy~77MzG82B6fOKDwgRr53fv~EqKF7XRnZrrIs2f~QxkZsRECTKaoDwveTENmnf73RkoRnZoc6i4J5Z2xUpxnWvLvNGFeo7AJJhDk1hjXeqNdwmrfDMeqGuT7-vO54dHdviSltLp20FbZc1y-GGgkarc0Pe9hJY0BjoB1KKYkZwY2kz-nxpilohOHcsf8K8niY7fM5WpgrpTR43LMRDgsnB-ziIWGBrMo8rS9P-w1IBZx3DpBXPWUC8aUkUd-Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Using_the_morphology_of_the_hominoid_distal_fibula_to_interpret_arboreality_in_Australopithecus_afarensis","translated_slug":"","page_count":54,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano 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Terrestriality","url":"https://www.academia.edu/Documents/in/Arboreality_Vs_Terrestriality"},{"id":191815,"name":"Biological evolution","url":"https://www.academia.edu/Documents/in/Biological_evolution"},{"id":219545,"name":"Fibula structure","url":"https://www.academia.edu/Documents/in/Fibula_structure"},{"id":473007,"name":"Early Hominins","url":"https://www.academia.edu/Documents/in/Early_Hominins"},{"id":519447,"name":"Hominidae","url":"https://www.academia.edu/Documents/in/Hominidae"},{"id":1298116,"name":"Hominoid Locomotion","url":"https://www.academia.edu/Documents/in/Hominoid_Locomotion"}],"urls":[{"id":40844191,"url":"https://arpi.unipi.it/bitstream/11568/750330/6/Marchi,%202015,%20JHE,%20Post-Print.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067158"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis"><img alt="Research paper thumbnail of Nature and relationships of Sahelanthropus tchadensis" class="work-thumbnail" src="https://attachments.academia-assets.com/113024834/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis">Nature and relationships of Sahelanthropus tchadensis</a></div><div class="wp-workCard_item"><span>Journal of Human Evolution</span><span>, Dec 1, 2020</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="265bdfdb2a5f927df43b8ec9e5b0bbb7" 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and Characteristics of Sahelanthropus tchadensis","grobid_abstract":"A partial left femur (TM 266-01-063) was recovered in July 2001 at Toros-Menalla, Chad, at the same fossiliferous location as the late Miocene holotype of Sahelanthropus tchadensis (the cranium TM 266-01-060-1). It was recognized as a probable primate femur in 2004 when one of the authors was undertaking a taphonomic survey of the fossil assemblages from Toros-Menalla. We are confident the TM 266 femoral shaft belongs to a hominid. It could sample a hominid hitherto unrepresented at Toros-Menalla, but a more parsimonious working hypothesis is that it belongs to S. tchadensis. The differences between TM 266 and the late Miocene Orrorin tugenensis partial femur BAR 1002 0 00, from Kenya, are consistent with maintaining at least a species-level distinction between S. tchadensis and O. tugenensis. The results of our preliminary functional analysis suggest the TM 266 femoral shaft belongs to an individual that was not habitually bipedal, something that should be taken into account when considering the relationships of S. tchadensis. The circumstances of its discovery should encourage researchers to check to see whether there is more postcranial evidence of S. tchadensis among the fossils recovered from Toros-Menalla.","publication_date":{"day":1,"month":12,"year":2020,"errors":{}},"publication_name":"Journal of Human Evolution","grobid_abstract_attachment_id":113024834},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067158/Nature_and_relationships_of_Sahelanthropus_tchadensis","translated_internal_url":"","created_at":"2024-04-04T06:35:00.481-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024834,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024834/thumbnails/1.jpg","file_name":"j.jhevol.2020.10289820240404-1-ti8u8p.pdf","download_url":"https://www.academia.edu/attachments/113024834/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Nature_and_relationships_of_Sahelanthrop.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024834/j.jhevol.2020.10289820240404-1-ti8u8p-libre.pdf?1712240485=\u0026response-content-disposition=attachment%3B+filename%3DNature_and_relationships_of_Sahelanthrop.pdf\u0026Expires=1733264551\u0026Signature=CfMB4xHO4AvV6vhhXfCiXMw7cHF~c4pIG67Wtv-YV1k35JtmxcZDhfy41DAbCZZw5E~8CGGcCJSY~wqPXjfdIJ0rxltb0mc12vbIuW-P4~exerN68QW2bLuwDOLms8mCuE9GF5cY2P0uHD0m~dk07IhmNJ8IXcKSDvv0elzq6KR4RdvHf0Ap22l3CNLInTvptrVr2NiKBJU4ZxLj2VkDZJB~H~QUHzwbXHpEHnScRuJ~HgNKj0T1qm66~ko9Iqw-xXzRfXLTLTsoDcDbCGeSrEeEtVDnr~wzbu~uIMayVWJEMnF5g7cw21jkMarfmcYUEiPZKqV~RAueTrz37FI9GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Nature_and_relationships_of_Sahelanthropus_tchadensis","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":113024834,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024834/thumbnails/1.jpg","file_name":"j.jhevol.2020.10289820240404-1-ti8u8p.pdf","download_url":"https://www.academia.edu/attachments/113024834/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Nature_and_relationships_of_Sahelanthrop.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024834/j.jhevol.2020.10289820240404-1-ti8u8p-libre.pdf?1712240485=\u0026response-content-disposition=attachment%3B+filename%3DNature_and_relationships_of_Sahelanthrop.pdf\u0026Expires=1733264551\u0026Signature=CfMB4xHO4AvV6vhhXfCiXMw7cHF~c4pIG67Wtv-YV1k35JtmxcZDhfy41DAbCZZw5E~8CGGcCJSY~wqPXjfdIJ0rxltb0mc12vbIuW-P4~exerN68QW2bLuwDOLms8mCuE9GF5cY2P0uHD0m~dk07IhmNJ8IXcKSDvv0elzq6KR4RdvHf0Ap22l3CNLInTvptrVr2NiKBJU4ZxLj2VkDZJB~H~QUHzwbXHpEHnScRuJ~HgNKj0T1qm66~ko9Iqw-xXzRfXLTLTsoDcDbCGeSrEeEtVDnr~wzbu~uIMayVWJEMnF5g7cw21jkMarfmcYUEiPZKqV~RAueTrz37FI9GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":261,"name":"Geography","url":"https://www.academia.edu/Documents/in/Geography"},{"id":392,"name":"Archaeology","url":"https://www.academia.edu/Documents/in/Archaeology"},{"id":767,"name":"Anthropology","url":"https://www.academia.edu/Documents/in/Anthropology"},{"id":772,"name":"Human Evolution","url":"https://www.academia.edu/Documents/in/Human_Evolution"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":66145,"name":"Hominin evolution","url":"https://www.academia.edu/Documents/in/Hominin_evolution"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":530866,"name":"Hominid Evolution","url":"https://www.academia.edu/Documents/in/Hominid_Evolution"},{"id":1131312,"name":"Academic","url":"https://www.academia.edu/Documents/in/Academic"}],"urls":[{"id":40844190,"url":"https://www.sciencedirect.com/science/article/am/pii/S0047248420301597"}]}, dispatcherData: dispatcherData }); 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Differences in locomotor behavior among the great apes (knuckle-walking vs. quadrumanous climbing) can produce biomechanical differences that may be elucidated by the parallel study of cross-sectional characteristics of metacarpals and metatarsals. The aim of this work is to study the cross-sectional geometric properties of these bones and their correlation with locomotor behavior in large-bodied hominoids. The comparisons between bending moments of metacarpals and metatarsals of the same ray furnished interesting results. Metacarpals III and especially IV of the knuckle-walking African apes were relatively stronger than those of humans and orangutans, and metatarsal V of humans was relatively stronger than those of the great apes. Interestingly, the relative robusticity of the metacarpal IV of the quadrumanous orangutan was between that of the African apes and that of humans. 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class="js-work-strip profile--work_container" data-work-id="117067155"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso"><img alt="Research paper thumbnail of The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso" class="work-thumbnail" src="https://attachments.academia-assets.com/113024836/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso">The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso</a></div><div class="wp-workCard_item"><span>Homo-journal of Comparative Human Biology</span><span>, 2002</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="36641da1409a839f8832de401680104c" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":113024836,"asset_id":117067155,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067155"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa 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$('.js-work-strip[data-work-id=117067155]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067155,"title":"The skeletal biology of two Italian peninsular Magna Graecia necropoles, Timmari and Montescaglioso","translated_title":"","metadata":{"publisher":"Elsevier BV","ai_title_tag":"Skeletal Analysis of Magna Graecia Necropoles: Timmari \u0026 Montescaglioso","grobid_abstract":"The aim of this work is to outline a general picture of life style and conditions of a population living in Magna Graecia between the 7th and the 4th c. BC by the study of human skeletal remains found in two necropoles from the Matera province, Timmari and Montescaglioso, neighbouring Metaponto, one of the main Ionian Greek colonies. The biological reconstruction was attempted by a holistic approach which foresees the use of anthropometric, anthroposcopic, palaeodemographic, palaeopathological data, the study of skeletal and dentoalveolar indicators of environmental stress and the integration with archaeological and historical information. Interpretation of the results was also based on comparisons with coeval sites from Central-Southern Italy, from Greece and with earlier and later sites from the same region. The two samples from Matera did not show appreciable differences with the other Southern Italian coeval series when compared on the basis of metric and morphometric traits. The comparison with Greek samples was hampered by the scarcity of pertinent data. A high level of muscular activity was observed in males and females, with males clearly more mobile than females. Sexual dimorphism and limb bone lateralisation were marked. Health conditions and nutritional status were good. Riassunto Lo scopo di questo lavoro è delineare un quadro generale dello stile di vita e delle condizioni generali della popolazione che viveva nella Magna Grecia nei secoli compresi tra il 7 th e il 4 th a.C. Allo scopo sono stati studiati i resti scheletrici umani provenienti da due necropoli situate in provincia di Matera, Timmari e Montescaglioso, vicino a Metaponto che è stata una delle più importanti colonie greche sullo Ionio. La ricostruzione biologica delle due popolazioni è stata effettuata mediante un approccio olistico che comprende il rilevamento dai dati antropometrici, antroposcopici, paleodemografici e paleopatologici insieme allo studio degli indicatori scheletrici e dentoalveolari di stress ambientale, il tutto integrato con informazioni di carattere storico e archeologico. I risultati di queste analisi sono inoltre stati messi a confronto con campioni scheletrici provenienti da siti coevi dell'Italia centrale e meridionale, dalla Grecia e dalla stessa regione ma antecedenti (neolitici) e posteriori (medievali). Sulla base dei caratteri metrici e morfometrici, i due campioni qui analizzati (Timmari e Montescaglioso Belvedere) non hanno mostrato differenze apprezzabili rispetto alle altre serie coeve provenienti dall'Italia meridionale. Il confronto con le serie provenienti da necropoli greche è stato reso difficile dalla scarsità di dati relativi. E' stato rilevato un alto grado di attività muscolare sia nei maschi sia nelle femmine, con i maschi che mostrano chiari segni di maggiore mobilità. Il dimorfismo sessuale e il grado di lateralizzazione degli arti è risultato marcato. In generale, i campioni qui analizzati sono risultati in buone condizioni nutrizionali e di salute.","publication_date":{"day":null,"month":null,"year":2002,"errors":{}},"publication_name":"Homo-journal of Comparative Human Biology","grobid_abstract_attachment_id":113024836},"translated_abstract":null,"internal_url":"https://www.academia.edu/117067155/The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso","translated_internal_url":"","created_at":"2024-04-04T06:34:59.881-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":113024836,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024836/thumbnails/1.jpg","file_name":"0018-442x-0003820240404-1-7tru40.pdf","download_url":"https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"The_skeletal_biology_of_two_Italian_peni.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024836/0018-442x-0003820240404-1-7tru40-libre.pdf?1712240479=\u0026response-content-disposition=attachment%3B+filename%3DThe_skeletal_biology_of_two_Italian_peni.pdf\u0026Expires=1733036086\u0026Signature=MAD9HWdqgjJzmIGFPsh-eDrBQePCZwNWaLLnLNZdic3BDV5RiFTzHhj~c70S~5vo9B4m5Y5~WyVUl7JB4OetEBvfSvf3ZBkMhgdCkKSkuhMMLnjFDhoafvQ7k~vjGrU2YN1WiIS~X8tw6ShLtxT3uaEinN6LCabbRvkXFgUlSasCynxN3TlZ3rozsV~LmyixBrzWV-leXLCd9W2rjbJ013PWQntQd6e~GVmL-y7yh14iHIyfod549GQPIwJOST-rZXF8m9RRwl0~X3nARfRRlpwJHUmeomkO2cdks5Ayg1CN5c6BO3CDwH0teehfvbnRHfZxRiy63CWJiv~T78NA9Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"The_skeletal_biology_of_two_Italian_peninsular_Magna_Graecia_necropoles_Timmari_and_Montescaglioso","translated_slug":"","page_count":20,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":113024836,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/113024836/thumbnails/1.jpg","file_name":"0018-442x-0003820240404-1-7tru40.pdf","download_url":"https://www.academia.edu/attachments/113024836/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"The_skeletal_biology_of_two_Italian_peni.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/113024836/0018-442x-0003820240404-1-7tru40-libre.pdf?1712240479=\u0026response-content-disposition=attachment%3B+filename%3DThe_skeletal_biology_of_two_Italian_peni.pdf\u0026Expires=1733036086\u0026Signature=MAD9HWdqgjJzmIGFPsh-eDrBQePCZwNWaLLnLNZdic3BDV5RiFTzHhj~c70S~5vo9B4m5Y5~WyVUl7JB4OetEBvfSvf3ZBkMhgdCkKSkuhMMLnjFDhoafvQ7k~vjGrU2YN1WiIS~X8tw6ShLtxT3uaEinN6LCabbRvkXFgUlSasCynxN3TlZ3rozsV~LmyixBrzWV-leXLCd9W2rjbJ013PWQntQd6e~GVmL-y7yh14iHIyfod549GQPIwJOST-rZXF8m9RRwl0~X3nARfRRlpwJHUmeomkO2cdks5Ayg1CN5c6BO3CDwH0teehfvbnRHfZxRiy63CWJiv~T78NA9Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":310,"name":"Demography","url":"https://www.academia.edu/Documents/in/Demography"},{"id":1704,"name":"Bioarchaeology","url":"https://www.academia.edu/Documents/in/Bioarchaeology"},{"id":5018,"name":"Anthropometry","url":"https://www.academia.edu/Documents/in/Anthropometry"},{"id":7471,"name":"Life Style","url":"https://www.academia.edu/Documents/in/Life_Style"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":30181,"name":"Gender Identity","url":"https://www.academia.edu/Documents/in/Gender_Identity"},{"id":44744,"name":"Sexual dimorphism","url":"https://www.academia.edu/Documents/in/Sexual_dimorphism"},{"id":45213,"name":"Italy","url":"https://www.academia.edu/Documents/in/Italy"},{"id":85909,"name":"Iron Age Italy","url":"https://www.academia.edu/Documents/in/Iron_Age_Italy"},{"id":90326,"name":"Fossils","url":"https://www.academia.edu/Documents/in/Fossils"},{"id":192551,"name":"Nutritional Status","url":"https://www.academia.edu/Documents/in/Nutritional_Status"},{"id":232534,"name":"Health Status","url":"https://www.academia.edu/Documents/in/Health_Status"},{"id":413192,"name":"Sex Factors","url":"https://www.academia.edu/Documents/in/Sex_Factors"},{"id":1208706,"name":"Environment","url":"https://www.academia.edu/Documents/in/Environment"},{"id":1256683,"name":"Bone and Bones","url":"https://www.academia.edu/Documents/in/Bone_and_Bones"},{"id":2677637,"name":"Sex Characteristics","url":"https://www.academia.edu/Documents/in/Sex_Characteristics"}],"urls":[{"id":40844187,"url":"https://doi.org/10.1078/0018-442x-00038"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="117067154"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/117067154/Three_dimensional_geometric_morphometric_analysis_of_the_first_metacarpal_distal_articular_surface_in_humans_great_apes_and_fossil_hominins"><img alt="Research paper thumbnail of Three-dimensional geometric morphometric analysis of the first metacarpal distal articular surface in humans, great apes and fossil hominins" class="work-thumbnail" src="https://attachments.academia-assets.com/113024845/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/117067154/Three_dimensional_geometric_morphometric_analysis_of_the_first_metacarpal_distal_articular_surface_in_humans_great_apes_and_fossil_hominins">Three-dimensional geometric morphometric analysis of the first metacarpal distal articular surface in humans, great apes and fossil hominins</a></div><div class="wp-workCard_item"><span>Journal of Human Evolution</span><span>, Jul 1, 2019</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="f429691f4f69b907c101e96b00ac7b15" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":113024845,"asset_id":117067154,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/113024845/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067154"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067154"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067154; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "f429691f4f69b907c101e96b00ac7b15" } } $('.js-work-strip[data-work-id=117067154]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067154,"title":"Three-dimensional geometric morphometric analysis of the first metacarpal distal articular surface in humans, great apes and fossil hominins","translated_title":"","metadata":{"publisher":"Elsevier BV","grobid_abstract":"Western gorillas (Gorilla gorilla) are known to climb significantly more often than eastern gorillas (Gorilla beringei), a behavioral distinction attributable to major differences in their respective habitats (i.e., highland vs. lowland). Genetic evidence suggests that the lineages leading to these taxa began diverging from one another between approximately 1 and 3 million years ago. Thus, gorillas offer a special opportunity to examine the degree to which morphology of recently diverged taxa may be \"fine-tuned\" to differing ecological requirements. Using three-dimensional (3D) geometric morphometrics, we compared talar morphology in a sample of 87 specimens including western (lowland), mountain (highland), and grauer gorillas (lowland and highland populations). Talar shape was captured with a series of landmarks and semilandmarks superimposed by generalized Procrustes analysis. A between-group principal components analysis of overall talar shape separates gorillas by ecological habitat and by taxon. An analysis of only the trochlea and lateral malleolar facet identifies subtle variations in trochlear shape between western lowland and lowland grauer gorillas, potentially indicative of convergent evolution of arboreal adaptations in the talus. Lastly, talar shape scales differently with centroid size for highland and lowland gorillas, suggesting that ankle morphology may track bodysize mediated variation in arboreal behaviors differently depending on ecological setting. Several of the observed shape differences are linked biomechanically to the facilitation of climbing in lowland gorillas and to stability and load-bearing on terrestrial substrates in the highland taxa, providing an important comparative model for studying morphological variation in groups known only from fossils (e.g., early hominins).","publication_date":{"day":1,"month":7,"year":2019,"errors":{}},"publication_name":"Journal of Human 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class="js-work-more-abstract-truncated">ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. I risultati dell’analisi dell’analisi biomeccanica dell’arto inferiore suggeriscono che i neolitici liguri fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che queste popolazioni conducessero attività di sussistenza prevalentemente pastorali.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067153"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067153"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067153; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067153]").text(description); $(".js-view-count[data-work-id=117067153]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067153; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067153']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067153, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067153]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067153,"title":"Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale","translated_title":"","metadata":{"abstract":"ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. I risultati dell’analisi dell’analisi biomeccanica dell’arto inferiore suggeriscono che i neolitici liguri fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che queste popolazioni conducessero attività di sussistenza prevalentemente pastorali.","publication_date":{"day":null,"month":null,"year":2014,"errors":{}}},"translated_abstract":"ABSTRACT In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. 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data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/117067148/Relative_robusticity_of_the_Homo_floresiensis_tibia_and_fibula">Relative robusticity of the Homo floresiensis tibia and fibula</a></div><div class="wp-workCard_item"><span>American Journal of Physical Anthropology</span><span>, 2011</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this spec...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this species retained primitive characteristics of body shape and interlimb proportions, the H. floresiensis fibula remains an unexamined part of the equation. The leg of modern humans reflects our status as habitual bipeds and is signaled by a gracile fibula relative to a more robust, weight-bearing tibia. This study investigated whether LB1, the type specimen of H. floresiensis, possesses a robust fibula or displays the gracile fibula that is the signature of our species. CT scans of the fibula and tibia of LB1 and a sample of small-bodied modern humans (N=10) were used to analyze cross-sectional geometric (CSG) properties (e.g., cortical area and polar section modulus, Zp) of the tibia and fibula at midshaft. These new data were added to the much larger sample published by Marchi (2007), which included modern humans, chimpanzees, gorillas, orangutans and gibbons. External contours of additional fossils of the genus Homo (e.g., OH 35, KNM-WT-15000) were also examined in order to evaluate when the modern condition arose during the course of human evolution. Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. This work was supported by grants from the Wenner-Gren Foundation, the Leakey Foundation, the National Geographic Society, and the Australian Research Council.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="117067148"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="117067148"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 117067148; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=117067148]").text(description); $(".js-view-count[data-work-id=117067148]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 117067148; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='117067148']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 117067148, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=117067148]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":117067148,"title":"Relative robusticity of the Homo floresiensis tibia and fibula","translated_title":"","metadata":{"abstract":"ABSTRACT Although previous studies of the long bones of Homo floresiensis revealed that this species retained primitive characteristics of body shape and interlimb proportions, the H. floresiensis fibula remains an unexamined part of the equation. 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Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. 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CT scans of the fibula and tibia of LB1 and a sample of small-bodied modern humans (N=10) were used to analyze cross-sectional geometric (CSG) properties (e.g., cortical area and polar section modulus, Zp) of the tibia and fibula at midshaft. These new data were added to the much larger sample published by Marchi (2007), which included modern humans, chimpanzees, gorillas, orangutans and gibbons. External contours of additional fossils of the genus Homo (e.g., OH 35, KNM-WT-15000) were also examined in order to evaluate when the modern condition arose during the course of human evolution. Results indicate that LB1 manifests tibial/fibular robusticity indistinguishable from that of modern humans. Analysis of external contours suggests that a gracile fibula arose relatively early in human evolution and was already in place by ~1.5 mya. Although analysis of hindlimb vs. forelimb CSG of LB1 suggested a diverse locomotor repertoire (Jungers et al., 2009), this study emphasizes the importance of habitual bipedalism in H. floresiensis. 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His studies dealt mainly with anthropology a...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Sergio Sergi was an Italian physical anthropologist. His studies dealt mainly with anthropology and human biology, though they ranged from primatology, to comparative anatomy, to anthropometry and to palaeoanthropology. Sergio Sergi is known for his interpretation of human evolution, seen as a succession of “cicli di forme” (shape cycles) referring to the shape of the skull. He was also in favour of a “pre-Neanderthal” hypothesis concerning modern human origins. His works in anthropology are acknowledged worldwide and they are still cited in the scientific literature, in particular his monographs on the skulls of Monte Circeo, Saccopastore 1 and Saccopastore 2. He expanded the traditional areas of anthropology by extending the research to all organic systems, including the limbs, the tegumental system, the muscles of facial expression, the mechanism of respiration of anthropoids, and with systematic research on the spinal cord of chimpanzee.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="38959e25628b26cd64477c6dc9f25912" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":57882350,"asset_id":37875691,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/57882350/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="37875691"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="37875691"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 37875691; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=37875691]").text(description); $(".js-view-count[data-work-id=37875691]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 37875691; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='37875691']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 37875691, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "38959e25628b26cd64477c6dc9f25912" } } $('.js-work-strip[data-work-id=37875691]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":37875691,"title":"Sergi, Sergio","translated_title":"","metadata":{"abstract":"Sergio Sergi was an Italian physical anthropologist. His studies dealt mainly with anthropology and human biology, though they ranged from primatology, to comparative anatomy, to anthropometry and to palaeoanthropology. Sergio Sergi is known for his interpretation of human evolution, seen as a succession of “cicli di forme” (shape cycles) referring to the shape of the skull. He was also in favour of a “pre-Neanderthal” hypothesis concerning modern human origins. His works in anthropology are acknowledged worldwide and they are still cited in the scientific literature, in particular his monographs on the skulls of Monte Circeo, Saccopastore 1 and Saccopastore 2. He expanded the traditional areas of anthropology by extending the research to all organic systems, including the limbs, the tegumental system, the muscles of facial expression, the mechanism of respiration of anthropoids, and with systematic research on the spinal cord of chimpanzee.","publication_date":{"day":null,"month":null,"year":2018,"errors":{}},"publication_name":"The International Encyclopedia of Biological Anthropology"},"translated_abstract":"Sergio Sergi was an Italian physical anthropologist. His studies dealt mainly with anthropology and human biology, though they ranged from primatology, to comparative anatomy, to anthropometry and to palaeoanthropology. Sergio Sergi is known for his interpretation of human evolution, seen as a succession of “cicli di forme” (shape cycles) referring to the shape of the skull. He was also in favour of a “pre-Neanderthal” hypothesis concerning modern human origins. His works in anthropology are acknowledged worldwide and they are still cited in the scientific literature, in particular his monographs on the skulls of Monte Circeo, Saccopastore 1 and Saccopastore 2. He expanded the traditional areas of anthropology by extending the research to all organic systems, including the limbs, the tegumental system, the muscles of facial expression, the mechanism of respiration of anthropoids, and with systematic research on the spinal cord of chimpanzee.","internal_url":"https://www.academia.edu/37875691/Sergi_Sergio","translated_internal_url":"","created_at":"2018-11-29T05:10:44.614-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":57882350,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/57882350/thumbnails/1.jpg","file_name":"Marchi_D._2018__Sergi__Sergio.pdf","download_url":"https://www.academia.edu/attachments/57882350/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Sergi_Sergio.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/57882350/Marchi_D._2018__Sergi__Sergio-libre.pdf?1543498045=\u0026response-content-disposition=attachment%3B+filename%3DSergi_Sergio.pdf\u0026Expires=1733229915\u0026Signature=K-BLANuYRVNbXWEYTLOpWYbs27iOb5IYpuLgC4~etdN~aHbX~UfIlH0793Bksr8UmUOHbl8vir5LJ1YNQbIXpmToiWF-xc005mfh53Y2c-7QiWGyyceeOjUPBZJUOs~qOo6jbJVZFWTdz9pATCCFKk~5ZBVe~rRFFLD41YazyxnOvWr6L7DLPJ4TqZVX3G5GC8G~AQthLsxZlB9MpYoy0XzrwEZWcAjVUQowbPFnuSFA-Hh3l2kZ2Q6s8GL1Mif17mR2~ze2Ert5uv93EeLqc~KG5PyQ0f-iRwQL-fp0nPk5PchtwOPfhKhDC8rphYk8ICUNvks4hwZr~afkfwzWIA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Sergi_Sergio","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":57882350,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/57882350/thumbnails/1.jpg","file_name":"Marchi_D._2018__Sergi__Sergio.pdf","download_url":"https://www.academia.edu/attachments/57882350/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Sergi_Sergio.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/57882350/Marchi_D._2018__Sergi__Sergio-libre.pdf?1543498045=\u0026response-content-disposition=attachment%3B+filename%3DSergi_Sergio.pdf\u0026Expires=1733229915\u0026Signature=K-BLANuYRVNbXWEYTLOpWYbs27iOb5IYpuLgC4~etdN~aHbX~UfIlH0793Bksr8UmUOHbl8vir5LJ1YNQbIXpmToiWF-xc005mfh53Y2c-7QiWGyyceeOjUPBZJUOs~qOo6jbJVZFWTdz9pATCCFKk~5ZBVe~rRFFLD41YazyxnOvWr6L7DLPJ4TqZVX3G5GC8G~AQthLsxZlB9MpYoy0XzrwEZWcAjVUQowbPFnuSFA-Hh3l2kZ2Q6s8GL1Mif17mR2~ze2Ert5uv93EeLqc~KG5PyQ0f-iRwQL-fp0nPk5PchtwOPfhKhDC8rphYk8ICUNvks4hwZr~afkfwzWIA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":81953,"name":"Neanderthals","url":"https://www.academia.edu/Documents/in/Neanderthals"},{"id":967464,"name":"Skeletal Morphology","url":"https://www.academia.edu/Documents/in/Skeletal_Morphology"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="19536338"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/19536338/Preface"><img alt="Research paper thumbnail of Preface" class="work-thumbnail" src="https://attachments.academia-assets.com/40680896/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/19536338/Preface">Preface</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">For decades, scientists have relied on the concept of mobility in describing activity patterns of...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">For decades, scientists have relied on the concept of mobility in describing activity patterns of past and present human populations. Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior. For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter. Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility. The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups). It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies. Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility). Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading).</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="947786b3419f3c77c4f5f2b89ae19197" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":40680896,"asset_id":19536338,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/40680896/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="19536338"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="19536338"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 19536338; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=19536338]").text(description); $(".js-view-count[data-work-id=19536338]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 19536338; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='19536338']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 19536338, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "947786b3419f3c77c4f5f2b89ae19197" } } $('.js-work-strip[data-work-id=19536338]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":19536338,"title":"Preface","translated_title":"","metadata":{"abstract":"For decades, scientists have relied on the concept of mobility in describing activity patterns of past and present human populations. Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior. For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter. Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility. The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups). It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies. Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility). Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading)."},"translated_abstract":"For decades, scientists have relied on the concept of mobility in describing activity patterns of past and present human populations. Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior. For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter. Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility. The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups). It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies. Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility). Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading).","internal_url":"https://www.academia.edu/19536338/Preface","translated_internal_url":"","created_at":"2015-12-07T06:28:16.590-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":40680896,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/40680896/thumbnails/1.jpg","file_name":"Carlson___Marchi__2014__Preaface.pdf","download_url":"https://www.academia.edu/attachments/40680896/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Preface.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/40680896/Carlson___Marchi__2014__Preaface-libre.pdf?1449498459=\u0026response-content-disposition=attachment%3B+filename%3DPreface.pdf\u0026Expires=1733229915\u0026Signature=KpNM9a~8F8uc-1J1LUBEpOSwN80VNLI1MvWImo1bnZmJW2SbK62loM0MqIyUVgIU9nV5ASaT3BjIMbbGqYVDLtaSal2r~uwicgz6OIX4IegTXqSsr~xBI2bB5nCZLkLa-tk54thY~qnBds9wgY3PQVgQedocolg119847VeJKB9FTSvImmdzswMFTzfoEkQ7rIZh~y4scc2hfv~n7U50CYTmQINum85xgYYuXdcq-LGnbmjnIk1vmoV29uIgZZ-0iBNVgespZRiq3lzFUNwNR94DRiHbI-3HaN~VQOzX8mI75QD0jUNvFU6c5QlEufLrJH~oc0VEBmlKRxOYELFHCw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Preface","translated_slug":"","page_count":2,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":40680896,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/40680896/thumbnails/1.jpg","file_name":"Carlson___Marchi__2014__Preaface.pdf","download_url":"https://www.academia.edu/attachments/40680896/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Preface.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/40680896/Carlson___Marchi__2014__Preaface-libre.pdf?1449498459=\u0026response-content-disposition=attachment%3B+filename%3DPreface.pdf\u0026Expires=1733229915\u0026Signature=KpNM9a~8F8uc-1J1LUBEpOSwN80VNLI1MvWImo1bnZmJW2SbK62loM0MqIyUVgIU9nV5ASaT3BjIMbbGqYVDLtaSal2r~uwicgz6OIX4IegTXqSsr~xBI2bB5nCZLkLa-tk54thY~qnBds9wgY3PQVgQedocolg119847VeJKB9FTSvImmdzswMFTzfoEkQ7rIZh~y4scc2hfv~n7U50CYTmQINum85xgYYuXdcq-LGnbmjnIk1vmoV29uIgZZ-0iBNVgespZRiq3lzFUNwNR94DRiHbI-3HaN~VQOzX8mI75QD0jUNvFU6c5QlEufLrJH~oc0VEBmlKRxOYELFHCw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":28941,"name":"Musculoskeletal Biomechanics","url":"https://www.academia.edu/Documents/in/Musculoskeletal_Biomechanics"},{"id":30824,"name":"Subsistance Strategies (Archaeology)","url":"https://www.academia.edu/Documents/in/Subsistance_Strategies_Archaeology_"},{"id":50690,"name":"Mobility","url":"https://www.academia.edu/Documents/in/Mobility"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="384114"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/384114/Chapter_13_Mobility_and_lower_limb_robusticity_of_a_pastoralist_Neolithic_population_from_North_Western_Italy"><img alt="Research paper thumbnail of Chapter 13. Mobility and lower limb robusticity of a pastoralist Neolithic population from North-Western Italy" class="work-thumbnail" src="https://attachments.academia-assets.com/1871758/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/384114/Chapter_13_Mobility_and_lower_limb_robusticity_of_a_pastoralist_Neolithic_population_from_North_Western_Italy">Chapter 13. Mobility and lower limb robusticity of a pastoralist Neolithic population from North-Western Italy</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Previous research on the transition from hunting and gathering to production economy has suggeste...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Previous research on the transition from hunting and gathering to production economy has suggested some general trends in past populations, i.e. decreased diaphyseal robusticity, increased cross-sectional circularity and decreased sexual dimorphism in the lower limb bones (femur and tibia), generally explained as a consequence of decreased levels of mobility. Previous results from the study of the Ligurian Neolithic populations from North-Western Italy (6th millennium BP) provide an exception to these trends. In particular, the Ligurian Neolithic lower limb robusticity and diaphyseal shape reflect high levels of terrestrial mobility throughout a rugged terrain. These results argue in favour of the growing consensus that the Neolithic transition was a region-specific process. In this work we expand the sample to include remains from caves from the same area, all within the same pastoral system, and extend the analysis to include the fibula. These new results show that the diaphyseal morphology of the Ligurian sample is more similar to highly mobile European Late Upper Palaeolithic and Mesolithic populations. Furthermore, the degree of sexual dimorphism for mechanical properties indicates behavioural differences between sexes, with males being more mobile than females. The results found here also indicate that inclusion of the fibula may contribute to a better understanding of past population mobility especially when it is considered in association with the tibia.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="61afb3a821173d99673f4fbc0093e747" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":1871758,"asset_id":384114,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/1871758/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="384114"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="384114"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 384114; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=384114]").text(description); $(".js-view-count[data-work-id=384114]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 384114; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='384114']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 384114, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "61afb3a821173d99673f4fbc0093e747" } } $('.js-work-strip[data-work-id=384114]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":384114,"title":"Chapter 13. Mobility and lower limb robusticity of a pastoralist Neolithic population from North-Western Italy","translated_title":"","metadata":{"abstract":"Previous research on the transition from hunting and gathering to production economy has suggested some general trends in past populations, i.e. decreased diaphyseal robusticity, increased cross-sectional circularity and decreased sexual dimorphism in the lower limb bones (femur and tibia), generally explained as a consequence of decreased levels of mobility. Previous results from the study of the Ligurian Neolithic populations from North-Western Italy (6th millennium BP) provide an exception to these trends. In particular, the Ligurian Neolithic lower limb robusticity and diaphyseal shape reflect high levels of terrestrial mobility throughout a rugged terrain. These results argue in favour of the growing consensus that the Neolithic transition was a region-specific process. In this work we expand the sample to include remains from caves from the same area, all within the same pastoral system, and extend the analysis to include the fibula. These new results show that the diaphyseal morphology of the Ligurian sample is more similar to highly mobile European Late Upper Palaeolithic and Mesolithic populations. Furthermore, the degree of sexual dimorphism for mechanical properties indicates behavioural differences between sexes, with males being more mobile than females. The results found here also indicate that inclusion of the fibula may contribute to a better understanding of past population mobility especially when it is considered in association with the tibia.","more_info":"In: \"Human Bioarchaeology of the Transition to Agriculture\", R. Pinhasi and JT Stock (Eds). p. 317-346.","publisher":"Wiley-Blackwell","publication_date":{"day":null,"month":null,"year":2011,"errors":{}}},"translated_abstract":"Previous research on the transition from hunting and gathering to production economy has suggested some general trends in past populations, i.e. decreased diaphyseal robusticity, increased cross-sectional circularity and decreased sexual dimorphism in the lower limb bones (femur and tibia), generally explained as a consequence of decreased levels of mobility. Previous results from the study of the Ligurian Neolithic populations from North-Western Italy (6th millennium BP) provide an exception to these trends. In particular, the Ligurian Neolithic lower limb robusticity and diaphyseal shape reflect high levels of terrestrial mobility throughout a rugged terrain. These results argue in favour of the growing consensus that the Neolithic transition was a region-specific process. In this work we expand the sample to include remains from caves from the same area, all within the same pastoral system, and extend the analysis to include the fibula. These new results show that the diaphyseal morphology of the Ligurian sample is more similar to highly mobile European Late Upper Palaeolithic and Mesolithic populations. Furthermore, the degree of sexual dimorphism for mechanical properties indicates behavioural differences between sexes, with males being more mobile than females. The results found here also indicate that inclusion of the fibula may contribute to a better understanding of past population mobility especially when it is considered in association with the tibia.","internal_url":"https://www.academia.edu/384114/Chapter_13_Mobility_and_lower_limb_robusticity_of_a_pastoralist_Neolithic_population_from_North_Western_Italy","translated_internal_url":"","created_at":"2010-12-06T00:19:17.976-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":1871758,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/1871758/thumbnails/1.jpg","file_name":"Proofs_Marchi_et_al..pdf","download_url":"https://www.academia.edu/attachments/1871758/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_13_Mobility_and_lower_limb_robus.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/1871758/Proofs_Marchi_et_al.-libre.pdf?1390823208=\u0026response-content-disposition=attachment%3B+filename%3DChapter_13_Mobility_and_lower_limb_robus.pdf\u0026Expires=1733229915\u0026Signature=beBY~B5raH~YyMc~8qa2DaiDCg2wNA9p9OCN-sLcV~tIvFPqRo3fq5-NW0VvZ1kcHicZSQc9TNhnvwggpRRbs3zJhy-7pALHRRWzFFr6FVVxbzw-W0heLK7ItLXpM3OiATM1Cfwe0MYpxSuw4UvlPTjeiQ85FjM6kogyZkwQ8qa1y2kN9cSeF8Vpsxk0hxyJs47YXrvoZSCSXSOyDaAbiOVCKC3jC3N5v4vi5FtusGb0NR3lQipLSo0VFVQfu3c30t1PvhaLIUeUzHmR6z9laiMY87CJBK4A81b5CqKl-n7yY3tP8GjV0CMF4r3SvwK2G4QCTOFwAVRQTtHesSKNXw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Chapter_13_Mobility_and_lower_limb_robusticity_of_a_pastoralist_Neolithic_population_from_North_Western_Italy","translated_slug":"","page_count":30,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":1871758,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/1871758/thumbnails/1.jpg","file_name":"Proofs_Marchi_et_al..pdf","download_url":"https://www.academia.edu/attachments/1871758/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_13_Mobility_and_lower_limb_robus.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/1871758/Proofs_Marchi_et_al.-libre.pdf?1390823208=\u0026response-content-disposition=attachment%3B+filename%3DChapter_13_Mobility_and_lower_limb_robus.pdf\u0026Expires=1733229915\u0026Signature=beBY~B5raH~YyMc~8qa2DaiDCg2wNA9p9OCN-sLcV~tIvFPqRo3fq5-NW0VvZ1kcHicZSQc9TNhnvwggpRRbs3zJhy-7pALHRRWzFFr6FVVxbzw-W0heLK7ItLXpM3OiATM1Cfwe0MYpxSuw4UvlPTjeiQ85FjM6kogyZkwQ8qa1y2kN9cSeF8Vpsxk0hxyJs47YXrvoZSCSXSOyDaAbiOVCKC3jC3N5v4vi5FtusGb0NR3lQipLSo0VFVQfu3c30t1PvhaLIUeUzHmR6z9laiMY87CJBK4A81b5CqKl-n7yY3tP8GjV0CMF4r3SvwK2G4QCTOFwAVRQTtHesSKNXw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":2409,"name":"Mobility/Mobilities","url":"https://www.academia.edu/Documents/in/Mobility_Mobilities"},{"id":18561,"name":"Lower Extremity Biomechanics","url":"https://www.academia.edu/Documents/in/Lower_Extremity_Biomechanics"},{"id":26086,"name":"Neolithic Europe","url":"https://www.academia.edu/Documents/in/Neolithic_Europe"},{"id":62617,"name":"Liguria","url":"https://www.academia.edu/Documents/in/Liguria"},{"id":219868,"name":"Tibia Fibula Biomechanics","url":"https://www.academia.edu/Documents/in/Tibia_Fibula_Biomechanics"},{"id":390582,"name":"Subsitence","url":"https://www.academia.edu/Documents/in/Subsitence"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="8008299"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/8008299/Chapter_6_The_Importance_of_Considering_Fibular_Robusticity_When_Inferring_the_Mobility_Patterns_of_Past_Populations"><img alt="Research paper thumbnail of Chapter 6. The Importance of Considering Fibular Robusticity When Inferring the Mobility Patterns of Past Populations" class="work-thumbnail" src="https://attachments.academia-assets.com/34854244/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/8008299/Chapter_6_The_Importance_of_Considering_Fibular_Robusticity_When_Inferring_the_Mobility_Patterns_of_Past_Populations">Chapter 6. The Importance of Considering Fibular Robusticity When Inferring the Mobility Patterns of Past Populations</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this chapter we investigate the lower limb structural rigidity (using cross-sectional geometri...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this chapter we investigate the lower limb structural rigidity (using cross-sectional geometric properties of the diaphyseal midshaft) within a sample of 124 individuals from the Late Upper Paleolithic, Neolithic and Iron Age from Italy, Medieval Germany, and twenty-first Century Britain (long distance runners, field hockey players, and sedentary controls). Late Upper Paleolithic, Neolithic and Iron Age samples were settled in rugged areas, whereas the other samples inhabited plain areas. The aim of this study is to assess whether fibular diaphyseal properties reflect mobility patterns or terrain properties in past populations. Both fibular rigidity and relative fibular rigidity ratio (fibula/tibia) have been analyzed. Results reveal that Late Upper Paleolithic, Neolithic and Iron Age samples show high fibular rigidity and have values of relative fibular rigidity that are most similar to modern hockey players. The relative fibular diaphyseal rigidity of hockey players has been previously explained as the consequence of their dynamic and repetitive change of direction. Late Upper Paleolithic and Neolithic individuals are thought to have been highly terrestrially mobile, while Iron Age people were probably fairly sedentary. However, all of the three groups lived in areas of uneven terrain. We concluded that fibular rigidity and relative fibular rigidity are influenced by factorsthat increase foot eversion/inversion such as frequent directional changes and uneven terrain. The results of this study suggest that inclusion of the fibula provides a valuable additional perspective that complements traditional predictions of mobility patterns based on the femur or the tibia alone.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2df0df9e57258d34282111736a9b1da1" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":34854244,"asset_id":8008299,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/34854244/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="8008299"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="8008299"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 8008299; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=8008299]").text(description); $(".js-view-count[data-work-id=8008299]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 8008299; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='8008299']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 8008299, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "2df0df9e57258d34282111736a9b1da1" } } $('.js-work-strip[data-work-id=8008299]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":8008299,"title":"Chapter 6. The Importance of Considering Fibular Robusticity When Inferring the Mobility Patterns of Past Populations","translated_title":"","metadata":{"abstract":"In this chapter we investigate the lower limb structural rigidity (using cross-sectional geometric properties of the diaphyseal midshaft) within a sample of 124 individuals from the Late Upper Paleolithic, Neolithic and Iron Age from Italy, Medieval Germany, and twenty-first Century Britain (long distance runners, field hockey players, and sedentary controls). Late Upper Paleolithic, Neolithic and Iron Age samples were settled in rugged areas, whereas the other samples inhabited plain areas. The aim of this study is to assess whether fibular diaphyseal properties reflect mobility patterns or terrain properties in past populations. Both fibular rigidity and relative fibular rigidity ratio (fibula/tibia) have been analyzed. Results reveal that Late Upper Paleolithic, Neolithic and Iron Age samples show high fibular rigidity and have values of relative fibular rigidity that are most similar to modern hockey players. The relative fibular diaphyseal rigidity of hockey players has been previously explained as the consequence of their dynamic and repetitive change of direction. Late Upper Paleolithic and Neolithic individuals are thought to have been highly terrestrially mobile, while Iron Age people were probably fairly sedentary. However, all of the three groups lived in areas of uneven terrain. We concluded that fibular rigidity and relative fibular rigidity are influenced by factorsthat increase foot eversion/inversion such as frequent directional changes and uneven terrain. The results of this study suggest that inclusion of the fibula provides a valuable additional perspective that complements traditional predictions of mobility patterns based on the femur or the tibia alone.","more_info":"In, K.J. Carlson and D. Marchi (eds.), Reconstructing Mobility: Environmental, Behavioral, and Morphological Determinants. p. 91-110.","publisher":"Springer","publication_date":{"day":15,"month":8,"year":2014,"errors":{}}},"translated_abstract":"In this chapter we investigate the lower limb structural rigidity (using cross-sectional geometric properties of the diaphyseal midshaft) within a sample of 124 individuals from the Late Upper Paleolithic, Neolithic and Iron Age from Italy, Medieval Germany, and twenty-first Century Britain (long distance runners, field hockey players, and sedentary controls). Late Upper Paleolithic, Neolithic and Iron Age samples were settled in rugged areas, whereas the other samples inhabited plain areas. The aim of this study is to assess whether fibular diaphyseal properties reflect mobility patterns or terrain properties in past populations. Both fibular rigidity and relative fibular rigidity ratio (fibula/tibia) have been analyzed. Results reveal that Late Upper Paleolithic, Neolithic and Iron Age samples show high fibular rigidity and have values of relative fibular rigidity that are most similar to modern hockey players. The relative fibular diaphyseal rigidity of hockey players has been previously explained as the consequence of their dynamic and repetitive change of direction. Late Upper Paleolithic and Neolithic individuals are thought to have been highly terrestrially mobile, while Iron Age people were probably fairly sedentary. However, all of the three groups lived in areas of uneven terrain. We concluded that fibular rigidity and relative fibular rigidity are influenced by factorsthat increase foot eversion/inversion such as frequent directional changes and uneven terrain. The results of this study suggest that inclusion of the fibula provides a valuable additional perspective that complements traditional predictions of mobility patterns based on the femur or the tibia alone.","internal_url":"https://www.academia.edu/8008299/Chapter_6_The_Importance_of_Considering_Fibular_Robusticity_When_Inferring_the_Mobility_Patterns_of_Past_Populations","translated_internal_url":"","created_at":"2014-08-18T01:00:31.150-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":34854244,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/34854244/thumbnails/1.jpg","file_name":"Sparacello_et_al.__2014__Book_Carlson___Marchi.pdf","download_url":"https://www.academia.edu/attachments/34854244/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_6_The_Importance_of_Considering.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/34854244/Sparacello_et_al.__2014__Book_Carlson___Marchi-libre.pdf?1411555501=\u0026response-content-disposition=attachment%3B+filename%3DChapter_6_The_Importance_of_Considering.pdf\u0026Expires=1733229915\u0026Signature=RdyUru~G2aB-aL6sjijFzNM87Y36-qkS6d8drrUuz7RpXoWzaXeD7p4H4WRHjmF5x2irGQhGeJkCfWQm3f~E0RsVJ28kmVQ3grskJ9Qf6sFepZJCuguHANiTZStzTjxIhEyb3FZhBhJoGPZwXsqys2wBIrkpMjg7ckU43B0tf2T7LH3CrSal1U5hgZuRK8A0ZtGx6s2qCfpZupqCv96T6v5NTXK~tbgXMYinaB7XZcan2VUaegjimrX2knIF7kS3j6nwAj--uxSM8lWfiDN2eAXRhIH4w7JCQNSDAw-xVqgEjZL9ULMe9KjYK-yToVgaprBW7nYZ3M2B8ER4erry6g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Chapter_6_The_Importance_of_Considering_Fibular_Robusticity_When_Inferring_the_Mobility_Patterns_of_Past_Populations","translated_slug":"","page_count":20,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":34854244,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/34854244/thumbnails/1.jpg","file_name":"Sparacello_et_al.__2014__Book_Carlson___Marchi.pdf","download_url":"https://www.academia.edu/attachments/34854244/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_6_The_Importance_of_Considering.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/34854244/Sparacello_et_al.__2014__Book_Carlson___Marchi-libre.pdf?1411555501=\u0026response-content-disposition=attachment%3B+filename%3DChapter_6_The_Importance_of_Considering.pdf\u0026Expires=1733229915\u0026Signature=RdyUru~G2aB-aL6sjijFzNM87Y36-qkS6d8drrUuz7RpXoWzaXeD7p4H4WRHjmF5x2irGQhGeJkCfWQm3f~E0RsVJ28kmVQ3grskJ9Qf6sFepZJCuguHANiTZStzTjxIhEyb3FZhBhJoGPZwXsqys2wBIrkpMjg7ckU43B0tf2T7LH3CrSal1U5hgZuRK8A0ZtGx6s2qCfpZupqCv96T6v5NTXK~tbgXMYinaB7XZcan2VUaegjimrX2knIF7kS3j6nwAj--uxSM8lWfiDN2eAXRhIH4w7JCQNSDAw-xVqgEjZL9ULMe9KjYK-yToVgaprBW7nYZ3M2B8ER4erry6g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"},{"id":34854223,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/34854223/thumbnails/1.jpg","file_name":"Sparacello_et_al.__2014__Book_Carlson___Marchi.pdf","download_url":"https://www.academia.edu/attachments/34854223/download_file","bulk_download_file_name":"Chapter_6_The_Importance_of_Considering.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/34854223/Sparacello_et_al.__2014__Book_Carlson___Marchi-libre.pdf?1411555505=\u0026response-content-disposition=attachment%3B+filename%3DChapter_6_The_Importance_of_Considering.pdf\u0026Expires=1733229915\u0026Signature=MgG4j4n3M5KHlSD9q0yExoy0L8-wpfS7DL5HLzNmLJgowPs3ebdb1uWwME3Qzm1Zbyc4odefCyZW2NoNg7MPrzITg5EjvpUkqpSQeafR-BizAeZUEsgRgf~Pvdchjjk-3JLgWoOWON7DB-fYJQdWmNTVbotIwtCEvoH8h8WjIqUgeq-Lk8w2LnYmejU5pP4-cVzgKqnucZ-qKxIJ0axRIsCpHOcIufkIhSxG1mVOPm37N4dAUH4~oSdsBSSQDLN1tAeYoYfsDxCbnTTSPP80KU7394uGPF~svc9srKdTeXCtDEChmHIKtNN8qOvXD~03~Rso6mN~0aAaJcvs94j38w__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":1704,"name":"Bioarchaeology","url":"https://www.academia.edu/Documents/in/Bioarchaeology"},{"id":71579,"name":"Cross-Sectional Geometry","url":"https://www.academia.edu/Documents/in/Cross-Sectional_Geometry"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":168989,"name":"Terrain Conformation","url":"https://www.academia.edu/Documents/in/Terrain_Conformation"},{"id":219868,"name":"Tibia Fibula Biomechanics","url":"https://www.academia.edu/Documents/in/Tibia_Fibula_Biomechanics"},{"id":366875,"name":"Fibulae","url":"https://www.academia.edu/Documents/in/Fibulae"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="9057071"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/9057071/Chapter_1_Introduction_Towards_Refining_the_Concept_of_mobility"><img alt="Research paper thumbnail of Chapter 1. Introduction: Towards Refining the Concept of mobility" class="work-thumbnail" src="https://attachments.academia-assets.com/35360369/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/9057071/Chapter_1_Introduction_Towards_Refining_the_Concept_of_mobility">Chapter 1. Introduction: Towards Refining the Concept of mobility</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Bone has an ability to model and remodel itself such that its distribution and material propertie...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Bone has an ability to model and remodel itself such that its distribution and material properties reflect factors occurring during the lifetime of an individual. Known factors influencing bone properties range from nonmechanical (e.g., age, sex, diet, health, and hormones) to mechanical ones (e.g., activity level and patterns). A lifetime accumulation of these inputs, therefore, should be reflected in the structure of bone diaphyses at the death of an individual. Inferring the inputs of these factors from long bone diaphyses of long dead individuals, whether Holocene agriculturalists or hunter-gatherers, or earlier human ancestors, depends in part on modern analogues being used to help identify and isolate the contributions of these factors. This chapter is both an introduction to and a synthesis of the collaborative effort that is recounted within the volume, and that is aimed at understanding the impact of human mobility as one such input to diaphyseal form.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="98ceec98683aa35998649cbf1b6b880a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":35360369,"asset_id":9057071,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/35360369/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="9057071"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="9057071"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 9057071; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=9057071]").text(description); $(".js-view-count[data-work-id=9057071]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 9057071; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='9057071']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 9057071, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "98ceec98683aa35998649cbf1b6b880a" } } $('.js-work-strip[data-work-id=9057071]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":9057071,"title":"Chapter 1. Introduction: Towards Refining the Concept of mobility","translated_title":"","metadata":{"abstract":"Bone has an ability to model and remodel itself such that its distribution and material properties reflect factors occurring during the lifetime of an individual. Known factors influencing bone properties range from nonmechanical (e.g., age, sex, diet, health, and hormones) to mechanical ones (e.g., activity level and patterns). A lifetime accumulation of these inputs, therefore, should be reflected in the structure of bone diaphyses at the death of an individual. Inferring the inputs of these factors from long bone diaphyses of long dead individuals, whether Holocene agriculturalists or hunter-gatherers, or earlier human ancestors, depends in part on modern analogues being used to help identify and isolate the contributions of these factors. This chapter is both an introduction to and a synthesis of the collaborative effort that is recounted within the volume, and that is aimed at understanding the impact of human mobility as one such input to diaphyseal form.","more_info":"In, K.J. Carlson and D. Marchi (eds.), Reconstructing Mobility: Environmental, Behavioral, and Morphological Determinants. p. 1-11.","publisher":"Springer","publication_date":{"day":6,"month":8,"year":2014,"errors":{}}},"translated_abstract":"Bone has an ability to model and remodel itself such that its distribution and material properties reflect factors occurring during the lifetime of an individual. Known factors influencing bone properties range from nonmechanical (e.g., age, sex, diet, health, and hormones) to mechanical ones (e.g., activity level and patterns). A lifetime accumulation of these inputs, therefore, should be reflected in the structure of bone diaphyses at the death of an individual. Inferring the inputs of these factors from long bone diaphyses of long dead individuals, whether Holocene agriculturalists or hunter-gatherers, or earlier human ancestors, depends in part on modern analogues being used to help identify and isolate the contributions of these factors. This chapter is both an introduction to and a synthesis of the collaborative effort that is recounted within the volume, and that is aimed at understanding the impact of human mobility as one such input to diaphyseal form.","internal_url":"https://www.academia.edu/9057071/Chapter_1_Introduction_Towards_Refining_the_Concept_of_mobility","translated_internal_url":"","created_at":"2014-10-31T20:35:03.327-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":35360369,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/35360369/thumbnails/1.jpg","file_name":"Carlson___Marchi__Chap._1.pdf","download_url":"https://www.academia.edu/attachments/35360369/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_1_Introduction_Towards_Refining.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/35360369/Carlson___Marchi__Chap._1-libre.pdf?1414813369=\u0026response-content-disposition=attachment%3B+filename%3DChapter_1_Introduction_Towards_Refining.pdf\u0026Expires=1733264551\u0026Signature=FTUPHj-BwFokFriKDCPlj-UVIupRg24cVMWUNpvQa09qjZFHMCXde76EgrhAxdqpd4caNkrDetuTEXQllmEZ2acvTPQ-VaYnbVVaAd9DjKKfF-s95e2MLApoPRxMzwRqK25aDU8ljje0v7M9RVxM3NnX-X~uKCKPxbes6l-aw1HlrguRRKz3ZsA7GAIuIvR~P~xL1miZ37YrTZC9I5WURgjuphcAg0jjE9VSvwtWkVvYVOOTcAVxefb-jZ4HSHbP0dzN7MIZw3ow9sqs7QsJH1C4Xlepi9HBy9en-3bFgUIODMnkl0WF6LzLHE9vdsD7YC59aVm~qaKurQT~ZND2ww__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Chapter_1_Introduction_Towards_Refining_the_Concept_of_mobility","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":35360369,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/35360369/thumbnails/1.jpg","file_name":"Carlson___Marchi__Chap._1.pdf","download_url":"https://www.academia.edu/attachments/35360369/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Chapter_1_Introduction_Towards_Refining.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/35360369/Carlson___Marchi__Chap._1-libre.pdf?1414813369=\u0026response-content-disposition=attachment%3B+filename%3DChapter_1_Introduction_Towards_Refining.pdf\u0026Expires=1733264551\u0026Signature=FTUPHj-BwFokFriKDCPlj-UVIupRg24cVMWUNpvQa09qjZFHMCXde76EgrhAxdqpd4caNkrDetuTEXQllmEZ2acvTPQ-VaYnbVVaAd9DjKKfF-s95e2MLApoPRxMzwRqK25aDU8ljje0v7M9RVxM3NnX-X~uKCKPxbes6l-aw1HlrguRRKz3ZsA7GAIuIvR~P~xL1miZ37YrTZC9I5WURgjuphcAg0jjE9VSvwtWkVvYVOOTcAVxefb-jZ4HSHbP0dzN7MIZw3ow9sqs7QsJH1C4Xlepi9HBy9en-3bFgUIODMnkl0WF6LzLHE9vdsD7YC59aVm~qaKurQT~ZND2ww__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":32948,"name":"Hunter-Gatherers (Anthropology)","url":"https://www.academia.edu/Documents/in/Hunter-Gatherers_Anthropology_"},{"id":279638,"name":"Bone Functional Adaptation","url":"https://www.academia.edu/Documents/in/Bone_Functional_Adaptation"},{"id":313518,"name":"Activity patterns","url":"https://www.academia.edu/Documents/in/Activity_patterns"},{"id":1495763,"name":"Travel distance","url":"https://www.academia.edu/Documents/in/Travel_distance"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="1178430" id="books"><div class="js-work-strip profile--work_container" data-work-id="6157123"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/6157123/Reconstructing_mobility_environmental_behavioral_and_morphological_determinants"><img alt="Research paper thumbnail of Reconstructing mobility: environmental, behavioral, and morphological determinants" class="work-thumbnail" src="https://attachments.academia-assets.com/33187170/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/6157123/Reconstructing_mobility_environmental_behavioral_and_morphological_determinants">Reconstructing mobility: environmental, behavioral, and morphological determinants</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Preface For decades, scientists have relied on the concept of mobility in describing activity pa...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Preface <br />For decades, scientists have relied on the concept of mobility in describing activity patterns of past and present human populations.  Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior.  For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter.  Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility.  The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups).  It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies.  Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility).  Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading). <br />On the other hand, an excessively narrow application of the concept of mobility, such as a mechanically-focused one, equally limits comparisons of results across studies.  Not all studies would (nor should) integrate experimental approaches in order to quantify mobility.  Resources necessary for the requisite acquisition of ground reaction force and kinematic data are not equally available to all researchers, and there are ethical and logistical constraints when studying human subjects.  Rather, the optimal solution for defining mobility, or fully capturing its essence, should embrace a multidisciplinary approach in how the concept is applied.  Despite such a long-standing and widespread reliance on the concept of mobility for reconstructing and comparing activity patterns and life histories of human populations, such an inclusive attempt at defining mobility has not yet been made. <br />To address this notable absence, in the spring of 2011, we organized a symposium on mobility at the 80th Annual Meeting of the American Association of Physical Anthropologists held in Minneapolis, MN.  The symposium assembled an array of experts using different approaches for quantifying and comparing the effects of mobility on postcranial musculoskeletal anatomy.  The symposium, and subsequent discussions, were aimed at embracing current perspectives and stimulating new ones that emphasized a holistic view of the interaction among intrinsic (i.e. skeletal) and extrinsic (i.e. environmental) factors relevant for quantifying and studying differential expression of mobility. Moreover, the symposium highlighted the importance of disentangling environmental effects some of which transcend traditional categorical groupings, such as coastal versus inland and/or mountainous versus flat terrain environments. <br />This volume emanates from the original symposium.  It is not intended to be the final word on the concept of mobility, but we hope that it will serve as a suitable starting point from which new discussion and future work can begin (or continue), perhaps with a renewed focus on critical issues identified herein or to be expanded laterally.  We also hope that this volume represents a useful advance by articulating a consensus working definition of mobility that can be widely applied in anthropological studies in order to overcome the lack of consistency in explicitly defining the concept of mobility that currently cripples the comparisons of results across studies. <br />There are a number of people we would like to thank, for this volume would not have materialized without the substantial efforts of many.  First, we would like to acknowledge the original participants in the 2011 symposium, not all of whom were able to contribute chapters to the volume for one reason or another.  The discussions that took place leading up to, during, and following the symposium helped shape this volume considerably.  Thank you for your contributions in driving this effort forwards.  We also would like to thank contributors to the volume who did not participate in the 2011 symposium for one reason or another.  Your contributions to the collective effort have broadened its scope in new, exciting ways.  Chapters were reviewed by a mix of fellow contributors, co-editors, and additional colleagues.  We are indebted to everyone who assisted with reviewing the individual chapters.  Thank you for your time and willingness to offer constructive suggestions.  Finally, we would like to thank Janet Slobodien, Jacob Gallay, and others at Springer Press for encouraging the efforts that ultimately led to this volume.  We are extremely grateful for this unwavering support throughout the entire process.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="002cdf25a3163bafaa382503878bd10d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":33187170,"asset_id":6157123,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/33187170/download_file?st=MTczMzI2MDk1MSw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="6157123"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="6157123"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 6157123; 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Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior. For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter. Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility. The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups). It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies. Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility). Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading).\r\nOn the other hand, an excessively narrow application of the concept of mobility, such as a mechanically-focused one, equally limits comparisons of results across studies. Not all studies would (nor should) integrate experimental approaches in order to quantify mobility. Resources necessary for the requisite acquisition of ground reaction force and kinematic data are not equally available to all researchers, and there are ethical and logistical constraints when studying human subjects. Rather, the optimal solution for defining mobility, or fully capturing its essence, should embrace a multidisciplinary approach in how the concept is applied. Despite such a long-standing and widespread reliance on the concept of mobility for reconstructing and comparing activity patterns and life histories of human populations, such an inclusive attempt at defining mobility has not yet been made.\r\nTo address this notable absence, in the spring of 2011, we organized a symposium on mobility at the 80th Annual Meeting of the American Association of Physical Anthropologists held in Minneapolis, MN. The symposium assembled an array of experts using different approaches for quantifying and comparing the effects of mobility on postcranial musculoskeletal anatomy. The symposium, and subsequent discussions, were aimed at embracing current perspectives and stimulating new ones that emphasized a holistic view of the interaction among intrinsic (i.e. skeletal) and extrinsic (i.e. environmental) factors relevant for quantifying and studying differential expression of mobility. Moreover, the symposium highlighted the importance of disentangling environmental effects some of which transcend traditional categorical groupings, such as coastal versus inland and/or mountainous versus flat terrain environments.\r\nThis volume emanates from the original symposium. It is not intended to be the final word on the concept of mobility, but we hope that it will serve as a suitable starting point from which new discussion and future work can begin (or continue), perhaps with a renewed focus on critical issues identified herein or to be expanded laterally. We also hope that this volume represents a useful advance by articulating a consensus working definition of mobility that can be widely applied in anthropological studies in order to overcome the lack of consistency in explicitly defining the concept of mobility that currently cripples the comparisons of results across studies.\r\nThere are a number of people we would like to thank, for this volume would not have materialized without the substantial efforts of many. First, we would like to acknowledge the original participants in the 2011 symposium, not all of whom were able to contribute chapters to the volume for one reason or another. The discussions that took place leading up to, during, and following the symposium helped shape this volume considerably. Thank you for your contributions in driving this effort forwards. We also would like to thank contributors to the volume who did not participate in the 2011 symposium for one reason or another. Your contributions to the collective effort have broadened its scope in new, exciting ways. Chapters were reviewed by a mix of fellow contributors, co-editors, and additional colleagues. We are indebted to everyone who assisted with reviewing the individual chapters. Thank you for your time and willingness to offer constructive suggestions. Finally, we would like to thank Janet Slobodien, Jacob Gallay, and others at Springer Press for encouraging the efforts that ultimately led to this volume. We are extremely grateful for this unwavering support throughout the entire process.","more_info":"Kristian Carlson \u0026 Damiano Marchi","publisher":"Springer","publication_date":{"day":15,"month":8,"year":2014,"errors":{}}},"translated_abstract":"Preface\r\nFor decades, scientists have relied on the concept of mobility in describing activity patterns of past and present human populations. Population-level comparisons have traditionally sought to demonstrate differential mobility (e.g., logistical or residential) amongst Pleistocene or Holocene Homo groups, using this as a basis for inferring convergent or contrasting adaptive behavior. For example, shifting from a hunter-gatherer to a more sedentary agricultural subsistence strategy generally has been associated with a relative decline in mobility associated with the latter. Substantial efforts have been devoted towards inferring which musculoskeletal adaptations best reflect such a potential shift in mobility. The central role of bipedalism in human locomotion predisposes lower limb musculoskeletal anatomy to feature prominently in these inferences, although it is important to note that expressions of mobility in other areas of the postcranium (e.g., the upper limb) are gaining traction in the field when studying select populations (e.g., coastal or island groups). It is problematic that often mobility is not defined a priori in precise enough terms to facilitate comparability of results across studies. Typically, some derivation of an ethnographic definition of mobility is adopted, whether explicitly recognized or not (e.g., populations with greater mobility travel farther than populations with lesser mobility). Usually, in applying the ethnographic definition, unstated motivations for travel focus on resource acquisition or intergroup relationships (e.g., trading).\r\nOn the other hand, an excessively narrow application of the concept of mobility, such as a mechanically-focused one, equally limits comparisons of results across studies. Not all studies would (nor should) integrate experimental approaches in order to quantify mobility. Resources necessary for the requisite acquisition of ground reaction force and kinematic data are not equally available to all researchers, and there are ethical and logistical constraints when studying human subjects. Rather, the optimal solution for defining mobility, or fully capturing its essence, should embrace a multidisciplinary approach in how the concept is applied. Despite such a long-standing and widespread reliance on the concept of mobility for reconstructing and comparing activity patterns and life histories of human populations, such an inclusive attempt at defining mobility has not yet been made.\r\nTo address this notable absence, in the spring of 2011, we organized a symposium on mobility at the 80th Annual Meeting of the American Association of Physical Anthropologists held in Minneapolis, MN. The symposium assembled an array of experts using different approaches for quantifying and comparing the effects of mobility on postcranial musculoskeletal anatomy. The symposium, and subsequent discussions, were aimed at embracing current perspectives and stimulating new ones that emphasized a holistic view of the interaction among intrinsic (i.e. skeletal) and extrinsic (i.e. environmental) factors relevant for quantifying and studying differential expression of mobility. Moreover, the symposium highlighted the importance of disentangling environmental effects some of which transcend traditional categorical groupings, such as coastal versus inland and/or mountainous versus flat terrain environments.\r\nThis volume emanates from the original symposium. It is not intended to be the final word on the concept of mobility, but we hope that it will serve as a suitable starting point from which new discussion and future work can begin (or continue), perhaps with a renewed focus on critical issues identified herein or to be expanded laterally. We also hope that this volume represents a useful advance by articulating a consensus working definition of mobility that can be widely applied in anthropological studies in order to overcome the lack of consistency in explicitly defining the concept of mobility that currently cripples the comparisons of results across studies.\r\nThere are a number of people we would like to thank, for this volume would not have materialized without the substantial efforts of many. First, we would like to acknowledge the original participants in the 2011 symposium, not all of whom were able to contribute chapters to the volume for one reason or another. The discussions that took place leading up to, during, and following the symposium helped shape this volume considerably. Thank you for your contributions in driving this effort forwards. We also would like to thank contributors to the volume who did not participate in the 2011 symposium for one reason or another. Your contributions to the collective effort have broadened its scope in new, exciting ways. Chapters were reviewed by a mix of fellow contributors, co-editors, and additional colleagues. We are indebted to everyone who assisted with reviewing the individual chapters. Thank you for your time and willingness to offer constructive suggestions. Finally, we would like to thank Janet Slobodien, Jacob Gallay, and others at Springer Press for encouraging the efforts that ultimately led to this volume. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="2384545" id="proceedings"><div class="js-work-strip profile--work_container" data-work-id="10372686"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/10372686/La_biomeccanica_applicata_allo_studio_delle_caratteristiche_locomotorie_degli_ominoidei"><img alt="Research paper thumbnail of La biomeccanica applicata allo studio delle caratteristiche locomotorie degli ominoidei" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/10372686/La_biomeccanica_applicata_allo_studio_delle_caratteristiche_locomotorie_degli_ominoidei">La biomeccanica applicata allo studio delle caratteristiche locomotorie degli ominoidei</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">This is the first attempt to study cross-sectional geometry (using a moulding technique in combin...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">This is the first attempt to study cross-sectional geometry (using a moulding technique in combination with biplanar radiography) of metacarpals II-V, metatarsals I-V, and the tibio-fibular complex at 50% length across a sample of chimpanzees, gorillas, orang-utans, gibbons, and humans and to shed some light on their relationship with locomotor behaviour. The best results were obtained comparing tibia and fibula, and metacarpals and metatarsals of the same ray. On the whole, cross-sectional characteristics of the tibio-fibular complex, metacarpal and metatarsal rays are strongly related to the locomotor behaviour of hominoids, and may be useful in elucidating locomotor adaptations of fossil specimens.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="10372686"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="10372686"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 10372686; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=10372686]").text(description); $(".js-view-count[data-work-id=10372686]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 10372686; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='10372686']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 10372686, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=10372686]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":10372686,"title":"La biomeccanica applicata allo studio delle caratteristiche locomotorie degli ominoidei","translated_title":"","metadata":{"abstract":"This is the first attempt to study cross-sectional geometry (using a moulding technique in combination with biplanar radiography) of metacarpals II-V, metatarsals I-V, and the tibio-fibular complex at 50% length across a sample of chimpanzees, gorillas, orang-utans, gibbons, and humans and to shed some light on their relationship with locomotor behaviour. The best results were obtained comparing tibia and fibula, and metacarpals and metatarsals of the same ray. On the whole, cross-sectional characteristics of the tibio-fibular complex, metacarpal and metatarsal rays are strongly related to the locomotor behaviour of hominoids, and may be useful in elucidating locomotor adaptations of fossil specimens."},"translated_abstract":"This is the first attempt to study cross-sectional geometry (using a moulding technique in combination with biplanar radiography) of metacarpals II-V, metatarsals I-V, and the tibio-fibular complex at 50% length across a sample of chimpanzees, gorillas, orang-utans, gibbons, and humans and to shed some light on their relationship with locomotor behaviour. The best results were obtained comparing tibia and fibula, and metacarpals and metatarsals of the same ray. 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Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. I risultati dell’analisi dell’analisi biomeccanica dell’arto inferiore suggeriscono che i neolitici liguri fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che queste popolazioni conducessero attività di sussistenza prevalentemente pastorali.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="10072744"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="10072744"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 10072744; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=10072744]").text(description); $(".js-view-count[data-work-id=10072744]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 10072744; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='10072744']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 10072744, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=10072744]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":10072744,"title":"Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale","translated_title":"","metadata":{"abstract":"In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. I risultati dell’analisi dell’analisi biomeccanica dell’arto inferiore suggeriscono che i neolitici liguri fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che queste popolazioni conducessero attività di sussistenza prevalentemente pastorali."},"translated_abstract":"In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri. Il metodo d’indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un alto livello di robustezza suggerendo un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione mostra per gli uomini un’elevata lateralizzazione, associabile a frequenti attivitá unimanuali, mentre per le donne la lateralizzazione è molto bassa e associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. I neolitici liguri non mostrano la riduzione nella robustezza dell’arto inferiore che è caratteristica del campione tardo neolitico di confronto, e risultano più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, gli uomini neolitici liguri risultano molto più robusti delle donne suggerendo una marcata differenziazione dei ruoli tra i sessi. I risultati dell’analisi dell’analisi biomeccanica dell’arto inferiore suggeriscono che i neolitici liguri fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che queste popolazioni conducessero attività di sussistenza prevalentemente pastorali.","internal_url":"https://www.academia.edu/10072744/Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale","translated_internal_url":"","created_at":"2015-01-08T08:22:56.236-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[],"slug":"Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale","translated_slug":"","page_count":null,"language":"it","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[],"research_interests":[{"id":1704,"name":"Bioarchaeology","url":"https://www.academia.edu/Documents/in/Bioarchaeology"},{"id":2409,"name":"Mobility/Mobilities","url":"https://www.academia.edu/Documents/in/Mobility_Mobilities"},{"id":41906,"name":"Neolithic","url":"https://www.academia.edu/Documents/in/Neolithic"},{"id":44744,"name":"Sexual dimorphism","url":"https://www.academia.edu/Documents/in/Sexual_dimorphism"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":148859,"name":"Cross-Sectional Study","url":"https://www.academia.edu/Documents/in/Cross-Sectional_Study"},{"id":360548,"name":"Humerus","url":"https://www.academia.edu/Documents/in/Humerus"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="384243"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/384243/CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS_OF_A_WESTERN_LIGURIA_NEOLITHIC_SAMPLE"><img alt="Research paper thumbnail of CROSS-SECTIONAL GEOMETRY OF THE HUMERUS OF A WESTERN LIGURIA NEOLITHIC SAMPLE" class="work-thumbnail" src="https://attachments.academia-assets.com/1871979/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/384243/CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS_OF_A_WESTERN_LIGURIA_NEOLITHIC_SAMPLE">CROSS-SECTIONAL GEOMETRY OF THE HUMERUS OF A WESTERN LIGURIA NEOLITHIC SAMPLE</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">ABSTRACT - The cross-sectional geometry (CSG) properties of the humerus of a sample composed of n...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">ABSTRACT - The cross-sectional geometry (CSG) properties of the humerus of a sample composed of nine males and eight females from three caves located in the Finalese region (Savona, Italy) have been analysed. The comparison with a European Late Upper Paleolithic sample showed unchanged humeral robusticity in females and increased humeral robusticity in males leading to an increase in sexual dimorphism, indicating different activity levels between genders probably as a consequence of sexual division of labour. Both sexes show a more rounded humeral diaphyseal circumference and decrease of lateralization probably related to an increase in activities that stressed both limbs in a similar way. In particular, the finding of grind stone in the archaeological record seems to explain the absence of lateralization in females, which might be related to the processing of cereals. Overall CSG results furnish further evidence for the hypothesis of a prevalently pastoral economy of the Neolithic people of Western Liguria.<br /><br />RIASSUNTO - Sono state analizzate le proprietà di geometria delle sezioni (CSG) in un campione composto da nove maschi e otto femmine proveniente da tre caverne della zona del Finalese (Savona, Italia). Dal confronto con un campione europeo del Paleolitico Superiore Recente risulta che la robustezza dell’omero nel campione femminile rimane invariata, mentre nel campione maschile aumenta. Ne risulta un incremento del dimorfismo sessuale, probabilmente come conseguenza della divisione del lavoro in base al sesso. Entrambi i sessi mostrano sezioni diafisarie dell’omero più circolari e una diminuzione della lateralizzazione, probabilmente legati all’aumento delle attività che impegnavano in misura simile entrambi gli arti. In particolare, il ritrovamento di macine in pietra tra i reperti archeologici sembra spiegare l’assenza di lateralizzazione nelle femmine, la quale potrebbe essere legata all’attività di macinazione dei cereali. In generale, i risultati di CSG supportano e forniscono ulteriori prove all’ipotesi di un’economia prevalentemente pastorale per le popolazioni neolitiche della Liguria Occidentale.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="03ca74cf21f09ef463b0353b6cdbc55d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":1871979,"asset_id":384243,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/1871979/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="384243"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="384243"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 384243; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=384243]").text(description); $(".js-view-count[data-work-id=384243]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 384243; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='384243']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 384243, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "03ca74cf21f09ef463b0353b6cdbc55d" } } $('.js-work-strip[data-work-id=384243]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":384243,"title":"CROSS-SECTIONAL GEOMETRY OF THE HUMERUS OF A WESTERN LIGURIA NEOLITHIC SAMPLE","translated_title":"","metadata":{"abstract":"ABSTRACT - The cross-sectional geometry (CSG) properties of the humerus of a sample composed of nine males and eight females from three caves located in the Finalese region (Savona, Italy) have been analysed. The comparison with a European Late Upper Paleolithic sample showed unchanged humeral robusticity in females and increased humeral robusticity in males leading to an increase in sexual dimorphism, indicating different activity levels between genders probably as a consequence of sexual division of labour. Both sexes show a more rounded humeral diaphyseal circumference and decrease of lateralization probably related to an increase in activities that stressed both limbs in a similar way. In particular, the finding of grind stone in the archaeological record seems to explain the absence of lateralization in females, which might be related to the processing of cereals. Overall CSG results furnish further evidence for the hypothesis of a prevalently pastoral economy of the Neolithic people of Western Liguria.\n\nRIASSUNTO - Sono state analizzate le proprietà di geometria delle sezioni (CSG) in un campione composto da nove maschi e otto femmine proveniente da tre caverne della zona del Finalese (Savona, Italia). Dal confronto con un campione europeo del Paleolitico Superiore Recente risulta che la robustezza dell’omero nel campione femminile rimane invariata, mentre nel campione maschile aumenta. Ne risulta un incremento del dimorfismo sessuale, probabilmente come conseguenza della divisione del lavoro in base al sesso. Entrambi i sessi mostrano sezioni diafisarie dell’omero più circolari e una diminuzione della lateralizzazione, probabilmente legati all’aumento delle attività che impegnavano in misura simile entrambi gli arti. In particolare, il ritrovamento di macine in pietra tra i reperti archeologici sembra spiegare l’assenza di lateralizzazione nelle femmine, la quale potrebbe essere legata all’attività di macinazione dei cereali. In generale, i risultati di CSG supportano e forniscono ulteriori prove all’ipotesi di un’economia prevalentemente pastorale per le popolazioni neolitiche della Liguria Occidentale.","more_info":"Atti del XVI Congresso degli Antropology Italiani (Genova, 29-31 ottobre 2005), Edicolors Publishing, p. 631-640. English \"Proceedings of the XVI Meeting of the Italian Anthropologists\""},"translated_abstract":"ABSTRACT - The cross-sectional geometry (CSG) properties of the humerus of a sample composed of nine males and eight females from three caves located in the Finalese region (Savona, Italy) have been analysed. The comparison with a European Late Upper Paleolithic sample showed unchanged humeral robusticity in females and increased humeral robusticity in males leading to an increase in sexual dimorphism, indicating different activity levels between genders probably as a consequence of sexual division of labour. Both sexes show a more rounded humeral diaphyseal circumference and decrease of lateralization probably related to an increase in activities that stressed both limbs in a similar way. In particular, the finding of grind stone in the archaeological record seems to explain the absence of lateralization in females, which might be related to the processing of cereals. Overall CSG results furnish further evidence for the hypothesis of a prevalently pastoral economy of the Neolithic people of Western Liguria.\n\nRIASSUNTO - Sono state analizzate le proprietà di geometria delle sezioni (CSG) in un campione composto da nove maschi e otto femmine proveniente da tre caverne della zona del Finalese (Savona, Italia). Dal confronto con un campione europeo del Paleolitico Superiore Recente risulta che la robustezza dell’omero nel campione femminile rimane invariata, mentre nel campione maschile aumenta. Ne risulta un incremento del dimorfismo sessuale, probabilmente come conseguenza della divisione del lavoro in base al sesso. Entrambi i sessi mostrano sezioni diafisarie dell’omero più circolari e una diminuzione della lateralizzazione, probabilmente legati all’aumento delle attività che impegnavano in misura simile entrambi gli arti. In particolare, il ritrovamento di macine in pietra tra i reperti archeologici sembra spiegare l’assenza di lateralizzazione nelle femmine, la quale potrebbe essere legata all’attività di macinazione dei cereali. In generale, i risultati di CSG supportano e forniscono ulteriori prove all’ipotesi di un’economia prevalentemente pastorale per le popolazioni neolitiche della Liguria Occidentale.","internal_url":"https://www.academia.edu/384243/CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS_OF_A_WESTERN_LIGURIA_NEOLITHIC_SAMPLE","translated_internal_url":"","created_at":"2010-12-06T03:06:21.195-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[{"id":32513671,"work_id":384243,"tagging_user_id":125165,"tagged_user_id":null,"co_author_invite_id":6834373,"email":"v***o@durham.ac.uk","display_order":0,"name":"Vitale Sparacello","title":"CROSS-SECTIONAL GEOMETRY OF THE HUMERUS OF A WESTERN LIGURIA NEOLITHIC SAMPLE"}],"downloadable_attachments":[{"id":1871979,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/1871979/thumbnails/1.jpg","file_name":"Marchi___Sparacello_-_Proceedings_of_the_XVI_Meeting_of_the_Italian_Anthropologists.pdf","download_url":"https://www.academia.edu/attachments/1871979/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/1871979/Marchi___Sparacello_-_Proceedings_of_the_XVI_Meeting_of_the_Italian_Anthropologists-libre.pdf?1390823216=\u0026response-content-disposition=attachment%3B+filename%3DCROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS.pdf\u0026Expires=1733264552\u0026Signature=NEXS4-~2cgXo1NpzUGHgXAZjzo8cT1lG41eJQ1sVvuZOOKsbVfxUdnfAvJ49CHcATd3pCcptrIZ7bJXl1Okwm~N7Vym3OhXt5OyWQRHFPP6ZCGw5lrDvB7dCRBiw4xd-PGTKrhFv-yAt-3UjlT50~LMQcbDv0sr3leoTzN9a1z0g-OIoyKxv0IUOqMerE4k3MMBhmSndTDaY0rwrj2YPv5rPenJ3m-DY1qJo9OtZad2CGFCrxBEjEH~aHpUE~QaQR4d5dnAH6Cu7jDsbg~vuXfaAn2F0fVtPKXHFLg4SJ211XuPvT3SGoX24UeBbalsZkw-h9Rv20qeUuuKO1NTlPw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS_OF_A_WESTERN_LIGURIA_NEOLITHIC_SAMPLE","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":1871979,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/1871979/thumbnails/1.jpg","file_name":"Marchi___Sparacello_-_Proceedings_of_the_XVI_Meeting_of_the_Italian_Anthropologists.pdf","download_url":"https://www.academia.edu/attachments/1871979/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"CROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/1871979/Marchi___Sparacello_-_Proceedings_of_the_XVI_Meeting_of_the_Italian_Anthropologists-libre.pdf?1390823216=\u0026response-content-disposition=attachment%3B+filename%3DCROSS_SECTIONAL_GEOMETRY_OF_THE_HUMERUS.pdf\u0026Expires=1733264552\u0026Signature=NEXS4-~2cgXo1NpzUGHgXAZjzo8cT1lG41eJQ1sVvuZOOKsbVfxUdnfAvJ49CHcATd3pCcptrIZ7bJXl1Okwm~N7Vym3OhXt5OyWQRHFPP6ZCGw5lrDvB7dCRBiw4xd-PGTKrhFv-yAt-3UjlT50~LMQcbDv0sr3leoTzN9a1z0g-OIoyKxv0IUOqMerE4k3MMBhmSndTDaY0rwrj2YPv5rPenJ3m-DY1qJo9OtZad2CGFCrxBEjEH~aHpUE~QaQR4d5dnAH6Cu7jDsbg~vuXfaAn2F0fVtPKXHFLg4SJ211XuPvT3SGoX24UeBbalsZkw-h9Rv20qeUuuKO1NTlPw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":1704,"name":"Bioarchaeology","url":"https://www.academia.edu/Documents/in/Bioarchaeology"},{"id":26086,"name":"Neolithic Europe","url":"https://www.academia.edu/Documents/in/Neolithic_Europe"},{"id":62617,"name":"Liguria","url":"https://www.academia.edu/Documents/in/Liguria"},{"id":219549,"name":"Upper limb biomechanics","url":"https://www.academia.edu/Documents/in/Upper_limb_biomechanics"},{"id":390582,"name":"Subsitence","url":"https://www.academia.edu/Documents/in/Subsitence"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="1178452" id="conferenceabstracts"><div class="js-work-strip profile--work_container" data-work-id="42823500"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/42823500/morphomap_an_R_package_for_analysis_of_diaphyseal_cortical_thickness_shape_and_cross_sectional_geometry"><img alt="Research paper thumbnail of morphomap: an R package for analysis of diaphyseal cortical thickness, shape and cross-sectional geometry" class="work-thumbnail" src="https://attachments.academia-assets.com/63055117/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/42823500/morphomap_an_R_package_for_analysis_of_diaphyseal_cortical_thickness_shape_and_cross_sectional_geometry">morphomap: an R package for analysis of diaphyseal cortical thickness, shape and cross-sectional geometry</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The cross-sectional geometry of long bones is commonly used to infer their biomechanical properti...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The cross-sectional geometry of long bones is<br />commonly used to infer their biomechanical<br />properties in investigations of past and present<br />primate locomotion as well as to assess intensity<br />and repetitiveness of physical activities, and<br />to estimate body mass. While cross-sectional<br />geometry has proved to be very useful for reconstructing<br />bone loading patterns, a limitation of the<br />technique has been that only a few cross sections<br />along the diaphysis can be analyzed. The advent<br />of virtual imaging and image processing offers<br />the prospect of semi automating the sectioning<br />and calculation of geometric properties at high<br />resolution. We present the morphomap package,<br />developed in the R environment, to extract cross<br />sections from long bone meshes at speci􀜪ed<br />intervals along the diaphysis and to calculate<br />two and three dimensional morphometric maps,<br />cross-sectional geometric parameters, and<br />semilandmarks on the periosteal and endosteal<br />contours of each cross section. We demonstrate<br />the validity of this computational tool by showing<br />that it obtains the same results as those from<br />manual and other computational approaches.<br />We then demonstrate the functionality of<br />morphomap in a comparison of human and<br />chimpanzee femora. The tool produces 61 cross<br />sections along each diaphysis, at increments of<br />1% between 20% and 80% of their biomechanical<br />length, automatically draws morphometric maps<br />and calculates the parameters described above.<br />The results illustrate the potential of morphomap<br />in identifying differences in diaphyses that can be<br />related to differences in locomotion and lifestyle in<br />living and fossil primates.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="ce0f79f5560ccef9773291fcbac9dfe9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":63055117,"asset_id":42823500,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/63055117/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="42823500"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="42823500"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 42823500; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=42823500]").text(description); $(".js-view-count[data-work-id=42823500]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 42823500; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='42823500']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 42823500, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "ce0f79f5560ccef9773291fcbac9dfe9" } } $('.js-work-strip[data-work-id=42823500]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":42823500,"title":"morphomap: an R package for analysis of diaphyseal cortical thickness, shape and cross-sectional geometry","translated_title":"","metadata":{"abstract":"The cross-sectional geometry of long bones is\ncommonly used to infer their biomechanical\nproperties in investigations of past and present\nprimate locomotion as well as to assess intensity\nand repetitiveness of physical activities, and\nto estimate body mass. While cross-sectional\ngeometry has proved to be very useful for reconstructing\nbone loading patterns, a limitation of the\ntechnique has been that only a few cross sections\nalong the diaphysis can be analyzed. The advent\nof virtual imaging and image processing offers\nthe prospect of semi automating the sectioning\nand calculation of geometric properties at high\nresolution. We present the morphomap package,\ndeveloped in the R environment, to extract cross\nsections from long bone meshes at speci􀜪ed\nintervals along the diaphysis and to calculate\ntwo and three dimensional morphometric maps,\ncross-sectional geometric parameters, and\nsemilandmarks on the periosteal and endosteal\ncontours of each cross section. We demonstrate\nthe validity of this computational tool by showing\nthat it obtains the same results as those from\nmanual and other computational approaches.\nWe then demonstrate the functionality of\nmorphomap in a comparison of human and\nchimpanzee femora. The tool produces 61 cross\nsections along each diaphysis, at increments of\n1% between 20% and 80% of their biomechanical\nlength, automatically draws morphometric maps\nand calculates the parameters described above.\nThe results illustrate the potential of morphomap\nin identifying differences in diaphyses that can be\nrelated to differences in locomotion and lifestyle in\nliving and fossil primates.","ai_title_tag":"morphomap: R Package for Diaphyseal Bone Geometry Analysis","publication_date":{"day":null,"month":null,"year":2020,"errors":{}}},"translated_abstract":"The cross-sectional geometry of long bones is\ncommonly used to infer their biomechanical\nproperties in investigations of past and present\nprimate locomotion as well as to assess intensity\nand repetitiveness of physical activities, and\nto estimate body mass. While cross-sectional\ngeometry has proved to be very useful for reconstructing\nbone loading patterns, a limitation of the\ntechnique has been that only a few cross sections\nalong the diaphysis can be analyzed. The advent\nof virtual imaging and image processing offers\nthe prospect of semi automating the sectioning\nand calculation of geometric properties at high\nresolution. We present the morphomap package,\ndeveloped in the R environment, to extract cross\nsections from long bone meshes at speci􀜪ed\nintervals along the diaphysis and to calculate\ntwo and three dimensional morphometric maps,\ncross-sectional geometric parameters, and\nsemilandmarks on the periosteal and endosteal\ncontours of each cross section. We demonstrate\nthe validity of this computational tool by showing\nthat it obtains the same results as those from\nmanual and other computational approaches.\nWe then demonstrate the functionality of\nmorphomap in a comparison of human and\nchimpanzee femora. The tool produces 61 cross\nsections along each diaphysis, at increments of\n1% between 20% and 80% of their biomechanical\nlength, automatically draws morphometric maps\nand calculates the parameters described above.\nThe results illustrate the potential of morphomap\nin identifying differences in diaphyses that can be\nrelated to differences in locomotion and lifestyle in\nliving and fossil primates.","internal_url":"https://www.academia.edu/42823500/morphomap_an_R_package_for_analysis_of_diaphyseal_cortical_thickness_shape_and_cross_sectional_geometry","translated_internal_url":"","created_at":"2020-04-22T13:16:40.349-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[{"id":34351290,"work_id":42823500,"tagging_user_id":125165,"tagged_user_id":7122493,"co_author_invite_id":null,"email":"a***o@gmail.com","affiliation":"Università degli Studi \"La Sapienza\" di Roma","display_order":1,"name":"Antonio Profico","title":"morphomap: an R package for analysis of diaphyseal cortical thickness, shape and cross-sectional geometry"},{"id":34351291,"work_id":42823500,"tagging_user_id":125165,"tagged_user_id":32259084,"co_author_invite_id":null,"email":"l***d@gmail.com","display_order":2,"name":"Luca Bondioli","title":"morphomap: an R package for analysis of diaphyseal cortical thickness, shape and cross-sectional geometry"}],"downloadable_attachments":[{"id":63055117,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/63055117/thumbnails/1.jpg","file_name":"Profico_et_al.__2020__Abstract20200422-36868-1o5zx0s.pdf","download_url":"https://www.academia.edu/attachments/63055117/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"morphomap_an_R_package_for_analysis_of_d.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/63055117/Profico_et_al.__2020__Abstract20200422-36868-1o5zx0s-libre.pdf?1587587088=\u0026response-content-disposition=attachment%3B+filename%3Dmorphomap_an_R_package_for_analysis_of_d.pdf\u0026Expires=1733229916\u0026Signature=TuVdrMSo56bWvCBy5jn7GgYR6aMRZZkNxDoK14YAgkCF85F0JmGIPSsJxD9~UJr67Fk5UKdVUFgDmV-P2XSPYv9LNF0feJdaRKW9~2Uinq9x59oAYukG7K84rVQB9G0lnmuxKfUvrljR0Ti~jYAYCetvJJA8b76izIX6~KOXC6A9vVT7mRQwMStOMM7WMHZuhG2GId-AazLZlyW-SxoSDSWMAKRzNSnHKqrF9S1SmSQ7lDqzH1XIPMJiY9r4SKHIFStm0hfTWfCD6qlGDVxZf5GI9hZNVCJTNrGvGWZsq3ER1MbeuJ1nAV9X287G8ajlQuWtilzLOp3Pmh-AjHy2GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"morphomap_an_R_package_for_analysis_of_diaphyseal_cortical_thickness_shape_and_cross_sectional_geometry","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":63055117,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/63055117/thumbnails/1.jpg","file_name":"Profico_et_al.__2020__Abstract20200422-36868-1o5zx0s.pdf","download_url":"https://www.academia.edu/attachments/63055117/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"morphomap_an_R_package_for_analysis_of_d.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/63055117/Profico_et_al.__2020__Abstract20200422-36868-1o5zx0s-libre.pdf?1587587088=\u0026response-content-disposition=attachment%3B+filename%3Dmorphomap_an_R_package_for_analysis_of_d.pdf\u0026Expires=1733229916\u0026Signature=TuVdrMSo56bWvCBy5jn7GgYR6aMRZZkNxDoK14YAgkCF85F0JmGIPSsJxD9~UJr67Fk5UKdVUFgDmV-P2XSPYv9LNF0feJdaRKW9~2Uinq9x59oAYukG7K84rVQB9G0lnmuxKfUvrljR0Ti~jYAYCetvJJA8b76izIX6~KOXC6A9vVT7mRQwMStOMM7WMHZuhG2GId-AazLZlyW-SxoSDSWMAKRzNSnHKqrF9S1SmSQ7lDqzH1XIPMJiY9r4SKHIFStm0hfTWfCD6qlGDVxZf5GI9hZNVCJTNrGvGWZsq3ER1MbeuJ1nAV9X287G8ajlQuWtilzLOp3Pmh-AjHy2GQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":2360,"name":"Geometric Morphometrics","url":"https://www.academia.edu/Documents/in/Geometric_Morphometrics"},{"id":3132,"name":"Biomechanics","url":"https://www.academia.edu/Documents/in/Biomechanics"},{"id":4438,"name":"Functional Morphology","url":"https://www.academia.edu/Documents/in/Functional_Morphology"},{"id":71579,"name":"Cross-Sectional Geometry","url":"https://www.academia.edu/Documents/in/Cross-Sectional_Geometry"},{"id":435540,"name":"Primate Locomotion","url":"https://www.academia.edu/Documents/in/Primate_Locomotion"},{"id":450525,"name":"Hominin Locomotion","url":"https://www.academia.edu/Documents/in/Hominin_Locomotion"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="32774141"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/32774141/Functional_adaptations_of_primate_forearm_and_leg_muscle_fiber_architecture"><img alt="Research paper thumbnail of Functional adaptations of primate forearm and leg muscle fiber architecture" class="work-thumbnail" src="https://attachments.academia-assets.com/52928127/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/32774141/Functional_adaptations_of_primate_forearm_and_leg_muscle_fiber_architecture">Functional adaptations of primate forearm and leg muscle fiber architecture</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The osteology of the fore- and hind-limbs has been correlated with locomotion, posture and substr...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The osteology of the fore- and hind-limbs<br />has been correlated with locomotion, posture<br />and substrate use in primates, but less attention<br />has been paid to myological adaptations.<br />Previously we presented data on the functional<br />correlates of primate forearm muscle fiber<br />architecture variables: fascicle length (FL), physiological<br />cross-sectional area (PCSA) and reduced<br />PCSA (RPCSA). Here, we greatly expand the sample to include 9 strepsirrhine, 15 platyrrhine,<br />and 20 catarrhine taxa spanning the entire size<br />range of the order (Microcebus to Gorilla), and we<br />also include fiber data from the leg.<br />Forearm muscle mass scales with positive<br />allometry across all primates. Catarrhines exhibit<br />positive allometry in their PCSA and RPCSA<br />indicating that larger catarrhines have relatively<br />stronger forearm muscles. While PCSA and<br />RPCSA scale with isometry for terrestrial species,<br />they scale with positive allometry for arboreal<br />ones – thus larger arboreal primates have relatively<br />stronger forearms. Surprisingly, there are<br />no differences in the forearm architecture of<br />quadrupeds (QUAD) when compared to vertical<br />clinging and leaping/suspensory species (VCL).<br />All leg strength variables (mass, PCSA, RPCSA)<br />scale with positive allometry, and speed/stretch<br />measure (FL) scales with isometry across the<br />sample. Thus, larger primates are relatively<br />stronger though not more flexible/faster. There is<br />no other phylogenetic signal in the leg muscles.<br />Arboreal primates have greater leg RPCSA and<br />QUAD have statistically heavier leg muscles than<br />VCL, though they are not greater in cross-sectional<br />area or reduced in FL.<br />Thus, postural and substrate use adaptations in<br />strength and speed substantially differ between<br />the fore- and hind-limbs.<br />This research was funded by NSF BCS-14-40599.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="381cf23e7594d7193ce866bde0c16682" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":52928127,"asset_id":32774141,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/52928127/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="32774141"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="32774141"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 32774141; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=32774141]").text(description); $(".js-view-count[data-work-id=32774141]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 32774141; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='32774141']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 32774141, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "381cf23e7594d7193ce866bde0c16682" } } $('.js-work-strip[data-work-id=32774141]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":32774141,"title":"Functional adaptations of primate forearm and leg muscle fiber architecture","translated_title":"","metadata":{"abstract":"The osteology of the fore- and hind-limbs\nhas been correlated with locomotion, posture\nand substrate use in primates, but less attention\nhas been paid to myological adaptations.\nPreviously we presented data on the functional\ncorrelates of primate forearm muscle fiber\narchitecture variables: fascicle length (FL), physiological\ncross-sectional area (PCSA) and reduced\nPCSA (RPCSA). Here, we greatly expand the sample to include 9 strepsirrhine, 15 platyrrhine,\nand 20 catarrhine taxa spanning the entire size\nrange of the order (Microcebus to Gorilla), and we\nalso include fiber data from the leg.\nForearm muscle mass scales with positive\nallometry across all primates. Catarrhines exhibit\npositive allometry in their PCSA and RPCSA\nindicating that larger catarrhines have relatively\nstronger forearm muscles. While PCSA and\nRPCSA scale with isometry for terrestrial species,\nthey scale with positive allometry for arboreal\nones – thus larger arboreal primates have relatively\nstronger forearms. Surprisingly, there are\nno differences in the forearm architecture of\nquadrupeds (QUAD) when compared to vertical\nclinging and leaping/suspensory species (VCL).\nAll leg strength variables (mass, PCSA, RPCSA)\nscale with positive allometry, and speed/stretch\nmeasure (FL) scales with isometry across the\nsample. Thus, larger primates are relatively\nstronger though not more flexible/faster. There is\nno other phylogenetic signal in the leg muscles.\nArboreal primates have greater leg RPCSA and\nQUAD have statistically heavier leg muscles than\nVCL, though they are not greater in cross-sectional\narea or reduced in FL.\nThus, postural and substrate use adaptations in\nstrength and speed substantially differ between\nthe fore- and hind-limbs.\nThis research was funded by NSF BCS-14-40599."},"translated_abstract":"The osteology of the fore- and hind-limbs\nhas been correlated with locomotion, posture\nand substrate use in primates, but less attention\nhas been paid to myological adaptations.\nPreviously we presented data on the functional\ncorrelates of primate forearm muscle fiber\narchitecture variables: fascicle length (FL), physiological\ncross-sectional area (PCSA) and reduced\nPCSA (RPCSA). Here, we greatly expand the sample to include 9 strepsirrhine, 15 platyrrhine,\nand 20 catarrhine taxa spanning the entire size\nrange of the order (Microcebus to Gorilla), and we\nalso include fiber data from the leg.\nForearm muscle mass scales with positive\nallometry across all primates. Catarrhines exhibit\npositive allometry in their PCSA and RPCSA\nindicating that larger catarrhines have relatively\nstronger forearm muscles. While PCSA and\nRPCSA scale with isometry for terrestrial species,\nthey scale with positive allometry for arboreal\nones – thus larger arboreal primates have relatively\nstronger forearms. Surprisingly, there are\nno differences in the forearm architecture of\nquadrupeds (QUAD) when compared to vertical\nclinging and leaping/suspensory species (VCL).\nAll leg strength variables (mass, PCSA, RPCSA)\nscale with positive allometry, and speed/stretch\nmeasure (FL) scales with isometry across the\nsample. Thus, larger primates are relatively\nstronger though not more flexible/faster. There is\nno other phylogenetic signal in the leg muscles.\nArboreal primates have greater leg RPCSA and\nQUAD have statistically heavier leg muscles than\nVCL, though they are not greater in cross-sectional\narea or reduced in FL.\nThus, postural and substrate use adaptations in\nstrength and speed substantially differ between\nthe fore- and hind-limbs.\nThis research was funded by NSF BCS-14-40599.","internal_url":"https://www.academia.edu/32774141/Functional_adaptations_of_primate_forearm_and_leg_muscle_fiber_architecture","translated_internal_url":"","created_at":"2017-05-02T08:00:20.054-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":52928127,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/52928127/thumbnails/1.jpg","file_name":"Abstract_AJPA.pdf","download_url":"https://www.academia.edu/attachments/52928127/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Functional_adaptations_of_primate_forear.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/52928127/Abstract_AJPA-libre.pdf?1493737338=\u0026response-content-disposition=attachment%3B+filename%3DFunctional_adaptations_of_primate_forear.pdf\u0026Expires=1733264552\u0026Signature=SwMmKwh1QPpMFDD8Q0MbSluoR7p6FJ~3xf0MPIC3IPnN8B-ugWgvgHf0xObYDtuvFlE3yL8amgDoTtTZjZuTjIm~gBTHFnJk7Zef7-fA-QCmGIdFhR93tcQPzcivte4Z4sRWAXxYBLu-kWZw~srOaot-b~14xs3wSHTn4eWgEYT~T7Pkhsiru57PD5VbZiVjeI0I4qyXRh6-sBsCzrRvcGGoZ1692oaehKAbeNMJVB5FZUl4lczpP2PYTVr5rkSPPU4PF-Gzntq4eDqKlFRybQb8kJsN5HCIAyo~HuqYfTomfNR5WAusCEeRRP9FGtuwYl~sfp6AXrs2zSIaaNFE8A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Functional_adaptations_of_primate_forearm_and_leg_muscle_fiber_architecture","translated_slug":"","page_count":2,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":52928127,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/52928127/thumbnails/1.jpg","file_name":"Abstract_AJPA.pdf","download_url":"https://www.academia.edu/attachments/52928127/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Functional_adaptations_of_primate_forear.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/52928127/Abstract_AJPA-libre.pdf?1493737338=\u0026response-content-disposition=attachment%3B+filename%3DFunctional_adaptations_of_primate_forear.pdf\u0026Expires=1733264552\u0026Signature=SwMmKwh1QPpMFDD8Q0MbSluoR7p6FJ~3xf0MPIC3IPnN8B-ugWgvgHf0xObYDtuvFlE3yL8amgDoTtTZjZuTjIm~gBTHFnJk7Zef7-fA-QCmGIdFhR93tcQPzcivte4Z4sRWAXxYBLu-kWZw~srOaot-b~14xs3wSHTn4eWgEYT~T7Pkhsiru57PD5VbZiVjeI0I4qyXRh6-sBsCzrRvcGGoZ1692oaehKAbeNMJVB5FZUl4lczpP2PYTVr5rkSPPU4PF-Gzntq4eDqKlFRybQb8kJsN5HCIAyo~HuqYfTomfNR5WAusCEeRRP9FGtuwYl~sfp6AXrs2zSIaaNFE8A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":9658,"name":"Locomotion","url":"https://www.academia.edu/Documents/in/Locomotion"},{"id":168993,"name":"Arboreality Vs Terrestriality","url":"https://www.academia.edu/Documents/in/Arboreality_Vs_Terrestriality"},{"id":504368,"name":"Muscle Fiber Architecture","url":"https://www.academia.edu/Documents/in/Muscle_Fiber_Architecture"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="32774088"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/32774088/Relative_fibular_strength_and_locomotor_behavior_in_OH_35_and_KNM_WT_15000"><img alt="Research paper thumbnail of Relative fibular strength and locomotor behavior in OH 35 and KNM-WT 15000" class="work-thumbnail" src="https://attachments.academia-assets.com/52928082/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/32774088/Relative_fibular_strength_and_locomotor_behavior_in_OH_35_and_KNM_WT_15000">Relative fibular strength and locomotor behavior in OH 35 and KNM-WT 15000</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Relative fibular/tibial strength has been demonstrated to be related to the degree of arboreality...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Relative fibular/tibial strength has been demonstrated<br />to be related to the degree of arboreality/<br />terrestriality in anthropoid primates. In this study<br />fibular/tibial strength was determined in OH 35,<br />a Homo habilis (or possibly Paranthropus boisei),<br />(1.8 myr) and KNM-WT 15000, a juvenile Homo<br />erectus, (1.5 myr), and was compared to modern<br />humans (n=79), chimpanzees (n=16), gorillas<br />(n=16) and orangutans (n=11). Ontogenetic<br />changes in fibular/tibial strength were also<br />analyzed due to KNM-WT 15000’s juvenile status.<br />Cross-sectional properties were derived from<br />multi-plane radiography and either CT sections<br />of casts (fossils) or external molds (extant). RMA<br />regressions were run on polar second moment<br />of area (J), a measure of torsional and average<br />bending rigidity, of the fibula against that of the<br />tibia for all extant species. Fossils were analyzed<br />using their relative deviations from each regression<br />line, expressed in SEE units. Great apes<br />differed significantly from humans in regression<br />line elevation, with relatively stronger fibulae. OH<br />35 fell in the center of the great ape distribution,<br />within 1 SEE of each great ape taxon, but 1.9 SEE<br />from humans. KNM-WT 15000 was more than<br />2 SEE from all great apes and within 0.6 SEE<br />of humans. This was not a result of his age, as<br />fibular/tibial strength slightly decreases with age<br />in humans. OH 35 has some human-like features;<br />however, the relative strength of the two bones<br />aligns the specimen with great apes, suggesting<br />a significant degree of arboreality. KNM-WT<br />15000 is demonstrated to be fully modern,<br />complimenting other evidence for complete<br />terrestrial bipedality.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="dc853adb57d049eed886f7f346622ac9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":52928082,"asset_id":32774088,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/52928082/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="32774088"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="32774088"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 32774088; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=32774088]").text(description); $(".js-view-count[data-work-id=32774088]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 32774088; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='32774088']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 32774088, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "dc853adb57d049eed886f7f346622ac9" } } $('.js-work-strip[data-work-id=32774088]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":32774088,"title":"Relative fibular strength and locomotor behavior in OH 35 and KNM-WT 15000","translated_title":"","metadata":{"abstract":"Relative fibular/tibial strength has been demonstrated\nto be related to the degree of arboreality/\nterrestriality in anthropoid primates. In this study\nfibular/tibial strength was determined in OH 35,\na Homo habilis (or possibly Paranthropus boisei),\n(1.8 myr) and KNM-WT 15000, a juvenile Homo\nerectus, (1.5 myr), and was compared to modern\nhumans (n=79), chimpanzees (n=16), gorillas\n(n=16) and orangutans (n=11). Ontogenetic\nchanges in fibular/tibial strength were also\nanalyzed due to KNM-WT 15000’s juvenile status.\nCross-sectional properties were derived from\nmulti-plane radiography and either CT sections\nof casts (fossils) or external molds (extant). RMA\nregressions were run on polar second moment\nof area (J), a measure of torsional and average\nbending rigidity, of the fibula against that of the\ntibia for all extant species. Fossils were analyzed\nusing their relative deviations from each regression\nline, expressed in SEE units. Great apes\ndiffered significantly from humans in regression\nline elevation, with relatively stronger fibulae. OH\n35 fell in the center of the great ape distribution,\nwithin 1 SEE of each great ape taxon, but 1.9 SEE\nfrom humans. KNM-WT 15000 was more than\n2 SEE from all great apes and within 0.6 SEE\nof humans. This was not a result of his age, as\nfibular/tibial strength slightly decreases with age\nin humans. OH 35 has some human-like features;\nhowever, the relative strength of the two bones\naligns the specimen with great apes, suggesting\na significant degree of arboreality. KNM-WT\n15000 is demonstrated to be fully modern,\ncomplimenting other evidence for complete\nterrestrial bipedality."},"translated_abstract":"Relative fibular/tibial strength has been demonstrated\nto be related to the degree of arboreality/\nterrestriality in anthropoid primates. In this study\nfibular/tibial strength was determined in OH 35,\na Homo habilis (or possibly Paranthropus boisei),\n(1.8 myr) and KNM-WT 15000, a juvenile Homo\nerectus, (1.5 myr), and was compared to modern\nhumans (n=79), chimpanzees (n=16), gorillas\n(n=16) and orangutans (n=11). Ontogenetic\nchanges in fibular/tibial strength were also\nanalyzed due to KNM-WT 15000’s juvenile status.\nCross-sectional properties were derived from\nmulti-plane radiography and either CT sections\nof casts (fossils) or external molds (extant). RMA\nregressions were run on polar second moment\nof area (J), a measure of torsional and average\nbending rigidity, of the fibula against that of the\ntibia for all extant species. Fossils were analyzed\nusing their relative deviations from each regression\nline, expressed in SEE units. Great apes\ndiffered significantly from humans in regression\nline elevation, with relatively stronger fibulae. OH\n35 fell in the center of the great ape distribution,\nwithin 1 SEE of each great ape taxon, but 1.9 SEE\nfrom humans. KNM-WT 15000 was more than\n2 SEE from all great apes and within 0.6 SEE\nof humans. This was not a result of his age, as\nfibular/tibial strength slightly decreases with age\nin humans. OH 35 has some human-like features;\nhowever, the relative strength of the two bones\naligns the specimen with great apes, suggesting\na significant degree of arboreality. KNM-WT\n15000 is demonstrated to be fully modern,\ncomplimenting other evidence for complete\nterrestrial bipedality.","internal_url":"https://www.academia.edu/32774088/Relative_fibular_strength_and_locomotor_behavior_in_OH_35_and_KNM_WT_15000","translated_internal_url":"","created_at":"2017-05-02T07:57:52.404-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":52928082,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/52928082/thumbnails/1.jpg","file_name":"Abstract_AJPA.pdf","download_url":"https://www.academia.edu/attachments/52928082/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Relative_fibular_strength_and_locomotor.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/52928082/Abstract_AJPA-libre.pdf?1493737288=\u0026response-content-disposition=attachment%3B+filename%3DRelative_fibular_strength_and_locomotor.pdf\u0026Expires=1733264552\u0026Signature=R3Tb7Hh~RmaP68s6CzRKN6mWMzqPJMWQAUvSQa3qrsHDU89jAE8VtWsAw4N0JkwLg1EaPVlRqjrl1x3rdzeeSOQ1dSFwOiqzjLz9Rs572G5JaCUsbFQ7RQfUcCB7W6PowmrtKt40szxgXTovX-G-KDDYEFiJaK-NfXDmUxhms8Uxa-aLKFNpZdhPbFgTJbP5elTCs9nfljM3k5ZQpU~it2szoFr4llea-mw4Lv5FUay2s1VGE-Hb1gEvI40UIrlg915DgYNMRs~dvpnD94LTfBWJ3c4EURu1BX-vympT5-WaUaEM2W49SK-cS0fcr1n10MVYPem8jZvAIg4fOHPZwg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Relative_fibular_strength_and_locomotor_behavior_in_OH_35_and_KNM_WT_15000","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":52928082,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/52928082/thumbnails/1.jpg","file_name":"Abstract_AJPA.pdf","download_url":"https://www.academia.edu/attachments/52928082/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Relative_fibular_strength_and_locomotor.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/52928082/Abstract_AJPA-libre.pdf?1493737288=\u0026response-content-disposition=attachment%3B+filename%3DRelative_fibular_strength_and_locomotor.pdf\u0026Expires=1733264552\u0026Signature=R3Tb7Hh~RmaP68s6CzRKN6mWMzqPJMWQAUvSQa3qrsHDU89jAE8VtWsAw4N0JkwLg1EaPVlRqjrl1x3rdzeeSOQ1dSFwOiqzjLz9Rs572G5JaCUsbFQ7RQfUcCB7W6PowmrtKt40szxgXTovX-G-KDDYEFiJaK-NfXDmUxhms8Uxa-aLKFNpZdhPbFgTJbP5elTCs9nfljM3k5ZQpU~it2szoFr4llea-mw4Lv5FUay2s1VGE-Hb1gEvI40UIrlg915DgYNMRs~dvpnD94LTfBWJ3c4EURu1BX-vympT5-WaUaEM2W49SK-cS0fcr1n10MVYPem8jZvAIg4fOHPZwg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":398,"name":"Paleoanthropology","url":"https://www.academia.edu/Documents/in/Paleoanthropology"},{"id":3132,"name":"Biomechanics","url":"https://www.academia.edu/Documents/in/Biomechanics"},{"id":135875,"name":"Homo Erectus","url":"https://www.academia.edu/Documents/in/Homo_Erectus"},{"id":311977,"name":"Homo Habilis","url":"https://www.academia.edu/Documents/in/Homo_Habilis"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="24659428"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/24659428/Relative_length_of_the_immature_Homo_naledi_tibia_U_W_101_1070_evidence_for_elongation_of_the_leg"><img alt="Research paper thumbnail of Relative length of the immature Homo naledi tibia U.W. 101-1070: evidence for elongation of the leg" class="work-thumbnail" src="https://attachments.academia-assets.com/44986963/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/24659428/Relative_length_of_the_immature_Homo_naledi_tibia_U_W_101_1070_evidence_for_elongation_of_the_leg">Relative length of the immature Homo naledi tibia U.W. 101-1070: evidence for elongation of the leg</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">It is largely held that the transition from Australopithecus to the genus Homo involved a shift i...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">It is largely held that the transition from Australopithecus to the genus Homo involved a shift in overall body proportions, including a relative lengthening of the lower limb, though<br />the degree to which hominin limb proportions changed and the proximate causes thereof remain contentious topics. The overall poor preservation of most articular surfaces and predominately fragmentary diaphyses in the mature Dinaledi<br />lower limb long bone sample preclude a definitive assessment of lower limb proportions based on this material alone. The U.W. 101-1070 immature tibia is the most complete H. naledi<br />lower limb element recovered to date, measuring 278 mm from the eminence of the tibial spines to the distal extent of the medial malleolus, and preserving nearly the entire medial condyle. To assess proportions, we evaluated tibia medial<br />condylar dimensions relative to tibia maximum length in U.W. 101-1070, other fossil hominin tibiae, and an ontogenetic sample of humans, chimpanzees, and gorillas. Results indicate that the U.W. 101-1070 tibia is very long relative to joint size – markedly differing from all extant species and comparative fossil hominin tibiae. The combination of an exceptionally small tibial articular surface (like many australopiths) and moderately long tibia, in H. naledi, appears autapomorphic in the hominin fossil record. Though the specific implications of this finding<br />are partially dependent on the geological age and phylogenetic position of H. naledi, U.W. 101-1070 provides an example of bone length/joint size decoupling relative to the human pattern.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="61a6051f1f2ee0eee78429e4691a50dd" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":44986963,"asset_id":24659428,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/44986963/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="24659428"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="24659428"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 24659428; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=24659428]").text(description); $(".js-view-count[data-work-id=24659428]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 24659428; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='24659428']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 24659428, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "61a6051f1f2ee0eee78429e4691a50dd" } } $('.js-work-strip[data-work-id=24659428]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":24659428,"title":"Relative length of the immature Homo naledi tibia U.W. 101-1070: evidence for elongation of the leg","translated_title":"","metadata":{"abstract":"It is largely held that the transition from Australopithecus to the genus Homo involved a shift in overall body proportions, including a relative lengthening of the lower limb, though\nthe degree to which hominin limb proportions changed and the proximate causes thereof remain contentious topics. The overall poor preservation of most articular surfaces and predominately fragmentary diaphyses in the mature Dinaledi\nlower limb long bone sample preclude a definitive assessment of lower limb proportions based on this material alone. The U.W. 101-1070 immature tibia is the most complete H. naledi\nlower limb element recovered to date, measuring 278 mm from the eminence of the tibial spines to the distal extent of the medial malleolus, and preserving nearly the entire medial condyle. To assess proportions, we evaluated tibia medial\ncondylar dimensions relative to tibia maximum length in U.W. 101-1070, other fossil hominin tibiae, and an ontogenetic sample of humans, chimpanzees, and gorillas. Results indicate that the U.W. 101-1070 tibia is very long relative to joint size – markedly differing from all extant species and comparative fossil hominin tibiae. The combination of an exceptionally small tibial articular surface (like many australopiths) and moderately long tibia, in H. naledi, appears autapomorphic in the hominin fossil record. Though the specific implications of this finding\nare partially dependent on the geological age and phylogenetic position of H. naledi, U.W. 101-1070 provides an example of bone length/joint size decoupling relative to the human pattern."},"translated_abstract":"It is largely held that the transition from Australopithecus to the genus Homo involved a shift in overall body proportions, including a relative lengthening of the lower limb, though\nthe degree to which hominin limb proportions changed and the proximate causes thereof remain contentious topics. The overall poor preservation of most articular surfaces and predominately fragmentary diaphyses in the mature Dinaledi\nlower limb long bone sample preclude a definitive assessment of lower limb proportions based on this material alone. The U.W. 101-1070 immature tibia is the most complete H. naledi\nlower limb element recovered to date, measuring 278 mm from the eminence of the tibial spines to the distal extent of the medial malleolus, and preserving nearly the entire medial condyle. To assess proportions, we evaluated tibia medial\ncondylar dimensions relative to tibia maximum length in U.W. 101-1070, other fossil hominin tibiae, and an ontogenetic sample of humans, chimpanzees, and gorillas. Results indicate that the U.W. 101-1070 tibia is very long relative to joint size – markedly differing from all extant species and comparative fossil hominin tibiae. The combination of an exceptionally small tibial articular surface (like many australopiths) and moderately long tibia, in H. naledi, appears autapomorphic in the hominin fossil record. Though the specific implications of this finding\nare partially dependent on the geological age and phylogenetic position of H. naledi, U.W. 101-1070 provides an example of bone length/joint size decoupling relative to the human pattern.","internal_url":"https://www.academia.edu/24659428/Relative_length_of_the_immature_Homo_naledi_tibia_U_W_101_1070_evidence_for_elongation_of_the_leg","translated_internal_url":"","created_at":"2016-04-22T06:39:09.638-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":44986963,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/44986963/thumbnails/1.jpg","file_name":"Abstract_Print_Walker_et_al.pdf","download_url":"https://www.academia.edu/attachments/44986963/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Relative_length_of_the_immature_Homo_nal.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/44986963/Abstract_Print_Walker_et_al-libre.pdf?1461332328=\u0026response-content-disposition=attachment%3B+filename%3DRelative_length_of_the_immature_Homo_nal.pdf\u0026Expires=1733229916\u0026Signature=YAcqQrFE3rGnav4gwQ3A-pRffMUVdK8tK3dGA0J3slUY3qVxKQe2xBbQ7E1HbbmJE-14V3twdgP1erxIvDpJHy4Bn7UNOYd1-askDGJ-CgzVqfdTfHEQtuYgcTLbfBac8u8RtBIh7y-Bw17syMAtb5nKFXjLxSCSEOQBqvRl-hm1XT1HTidgiveGa1yzqRPfRf5lKgz5vgEHabjLFeZTaluzc~ehrnqJrmLy8N3PjqQ~VMoii6I7KVzoWnGG2xIxf2PyiIiKFSFC9TaZvF7n7THHr1lIlrflg95XbLjQFKNh16dUjUTU7Mgf~XfI1JnGEfqH2RThLA~Ht3v-0PjThg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Relative_length_of_the_immature_Homo_naledi_tibia_U_W_101_1070_evidence_for_elongation_of_the_leg","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":44986963,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/44986963/thumbnails/1.jpg","file_name":"Abstract_Print_Walker_et_al.pdf","download_url":"https://www.academia.edu/attachments/44986963/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Relative_length_of_the_immature_Homo_nal.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/44986963/Abstract_Print_Walker_et_al-libre.pdf?1461332328=\u0026response-content-disposition=attachment%3B+filename%3DRelative_length_of_the_immature_Homo_nal.pdf\u0026Expires=1733229916\u0026Signature=YAcqQrFE3rGnav4gwQ3A-pRffMUVdK8tK3dGA0J3slUY3qVxKQe2xBbQ7E1HbbmJE-14V3twdgP1erxIvDpJHy4Bn7UNOYd1-askDGJ-CgzVqfdTfHEQtuYgcTLbfBac8u8RtBIh7y-Bw17syMAtb5nKFXjLxSCSEOQBqvRl-hm1XT1HTidgiveGa1yzqRPfRf5lKgz5vgEHabjLFeZTaluzc~ehrnqJrmLy8N3PjqQ~VMoii6I7KVzoWnGG2xIxf2PyiIiKFSFC9TaZvF7n7THHr1lIlrflg95XbLjQFKNh16dUjUTU7Mgf~XfI1JnGEfqH2RThLA~Ht3v-0PjThg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":561304,"name":"Lower limb","url":"https://www.academia.edu/Documents/in/Lower_limb"},{"id":1737745,"name":"The Rising Star","url":"https://www.academia.edu/Documents/in/The_Rising_Star"},{"id":2104284,"name":"Homo naledi","url":"https://www.academia.edu/Documents/in/Homo_naledi"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="24659293"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/24659293/Homo_naledi_strides_again_preliminary_reconstructions_of_an_extinct_hominin_s_gait"><img alt="Research paper thumbnail of Homo naledi strides again: preliminary reconstructions of an extinct hominin’s gait" class="work-thumbnail" src="https://attachments.academia-assets.com/44986865/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/24659293/Homo_naledi_strides_again_preliminary_reconstructions_of_an_extinct_hominin_s_gait">Homo naledi strides again: preliminary reconstructions of an extinct hominin’s gait</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In this preliminary reconstruction of Homo naledi’s gait we begin with the null hypothesis that i...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In this preliminary reconstruction of Homo naledi’s gait we begin with the null hypothesis that it walked similarly to modern humans, as the overall anatomy of this extinct hominin’s lower limb, especially its foot, is mostly modern<br />human-like. We note the following characters as modern-like: dorsally-canting metatarsophalangeal joints facilitating toe-off, locking transverse tarsal joint implying a rigid midfoot during stance, flat subtalar joint limiting ankle pro- and supination, talocrural joint oriented orthogonally to the substrate, valgus knee, thick patellae increasing the moment arm for quadriceps femoris, and well-developed thigh muscle attachment sites throughout the femur. These characters suggest Homo naledi was welladapted to a striding bipedal gait. However, we also note the following less modern-like characters: curved pedal phalanges, low sustentaculum tali and likely a low fundamental<br />longitudinal arch, pronounced tubercular insertion of the pes anserinus tendon on the proximomedial tibia, long femoral neck with a marked medial encroachment of the obturator<br />externus, posteriorly positioned ilium relative to the acetabulum, flared iliac blades, broad lower ribcage, and characters of the lower thoracic vertebrae and lower rib suggesting robust hypaxial muscles. We offer our initial functional interpretations of the cumulative postcranial<br />morphology, which suggests different trunk stabilization from modern humans but is consistent with orthogrady and an obligate bipedal locomotor regime. Given the anatomy of<br />the upper limb, Homo naledi demonstrates coexistence of both bipedalism and climbing adaptations in one hominin taxon.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c349e4285e8acd11ea6bccea5b9ae447" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":44986865,"asset_id":24659293,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/44986865/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="24659293"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="24659293"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 24659293; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=24659293]").text(description); $(".js-view-count[data-work-id=24659293]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 24659293; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='24659293']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 24659293, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "c349e4285e8acd11ea6bccea5b9ae447" } } $('.js-work-strip[data-work-id=24659293]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":24659293,"title":"Homo naledi strides again: preliminary reconstructions of an extinct hominin’s gait","translated_title":"","metadata":{"abstract":"In this preliminary reconstruction of Homo naledi’s gait we begin with the null hypothesis that it walked similarly to modern humans, as the overall anatomy of this extinct hominin’s lower limb, especially its foot, is mostly modern\nhuman-like. We note the following characters as modern-like: dorsally-canting metatarsophalangeal joints facilitating toe-off, locking transverse tarsal joint implying a rigid midfoot during stance, flat subtalar joint limiting ankle pro- and supination, talocrural joint oriented orthogonally to the substrate, valgus knee, thick patellae increasing the moment arm for quadriceps femoris, and well-developed thigh muscle attachment sites throughout the femur. These characters suggest Homo naledi was welladapted to a striding bipedal gait. However, we also note the following less modern-like characters: curved pedal phalanges, low sustentaculum tali and likely a low fundamental\nlongitudinal arch, pronounced tubercular insertion of the pes anserinus tendon on the proximomedial tibia, long femoral neck with a marked medial encroachment of the obturator\nexternus, posteriorly positioned ilium relative to the acetabulum, flared iliac blades, broad lower ribcage, and characters of the lower thoracic vertebrae and lower rib suggesting robust hypaxial muscles. We offer our initial functional interpretations of the cumulative postcranial\nmorphology, which suggests different trunk stabilization from modern humans but is consistent with orthogrady and an obligate bipedal locomotor regime. Given the anatomy of\nthe upper limb, Homo naledi demonstrates coexistence of both bipedalism and climbing adaptations in one hominin taxon. "},"translated_abstract":"In this preliminary reconstruction of Homo naledi’s gait we begin with the null hypothesis that it walked similarly to modern humans, as the overall anatomy of this extinct hominin’s lower limb, especially its foot, is mostly modern\nhuman-like. We note the following characters as modern-like: dorsally-canting metatarsophalangeal joints facilitating toe-off, locking transverse tarsal joint implying a rigid midfoot during stance, flat subtalar joint limiting ankle pro- and supination, talocrural joint oriented orthogonally to the substrate, valgus knee, thick patellae increasing the moment arm for quadriceps femoris, and well-developed thigh muscle attachment sites throughout the femur. These characters suggest Homo naledi was welladapted to a striding bipedal gait. However, we also note the following less modern-like characters: curved pedal phalanges, low sustentaculum tali and likely a low fundamental\nlongitudinal arch, pronounced tubercular insertion of the pes anserinus tendon on the proximomedial tibia, long femoral neck with a marked medial encroachment of the obturator\nexternus, posteriorly positioned ilium relative to the acetabulum, flared iliac blades, broad lower ribcage, and characters of the lower thoracic vertebrae and lower rib suggesting robust hypaxial muscles. We offer our initial functional interpretations of the cumulative postcranial\nmorphology, which suggests different trunk stabilization from modern humans but is consistent with orthogrady and an obligate bipedal locomotor regime. Given the anatomy of\nthe upper limb, Homo naledi demonstrates coexistence of both bipedalism and climbing adaptations in one hominin taxon. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="24659217"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/24659217/Thigh_and_leg_remains_of_Homo_naledi"><img alt="Research paper thumbnail of Thigh and leg remains of Homo naledi" class="work-thumbnail" src="https://attachments.academia-assets.com/44986372/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/24659217/Thigh_and_leg_remains_of_Homo_naledi">Thigh and leg remains of Homo naledi</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in So...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20<br />out of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly,<br />running. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of<br />the pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species<br />intermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="826bbc2e5739c1838145ada1a7ff9991" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":44986372,"asset_id":24659217,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/44986372/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="24659217"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="24659217"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 24659217; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=24659217]").text(description); $(".js-view-count[data-work-id=24659217]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 24659217; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='24659217']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 24659217, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "826bbc2e5739c1838145ada1a7ff9991" } } $('.js-work-strip[data-work-id=24659217]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":24659217,"title":"Thigh and leg remains of Homo naledi","translated_title":"","metadata":{"abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20\nout of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly,\nrunning. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of\nthe pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species\nintermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus."},"translated_abstract":"Rising Star Cave is located in the Cradle of Humankind World Heritage site near Krugersdorp in South Africa. In November 2013 and March 2014 more than 1500 hominin fossil elements attributed to a new species, Homo naledi, were recovered and catalogued representing at least a dozen individuals. Only 20\nout of 206 bones in the human body are not in the collection as currently represented from the excavation. The thigh and leg of H. naledi, which are represented by 121 femoral, patellar, tibial, and fibular elements, are marked by a mosaic of primitive, derived, and unique traits that are functionally indicative of a bipedal hominin capable of long distance walking and, possibly,\nrunning. Traits shared with australopiths include a long, tall, and anteverted femoral neck, a mediolaterally compressed tibia, and a relatively circular fibular neck. Derived traits shared with Homo include a well-marked linea aspera, anteroposteriorly thick patellae, relatively long tibiae, and gracile fibulae with laterally oriented lateral malleoli. Unique features include the presence of two pillars on the superior aspect of the femoral neck and a strong distal insertion of\nthe pes anserinus on the tibia. The mosaic morphology of the H. naledi thigh and leg appears most consistent with a species\nintermediate between Australopithecus spp. and H. erectus and, accordingly, may offer insight into the nature of the Australopithecus-Homo morphological transition. These fossils also expand the morphological diversity of the Homo lower limb, perhaps indicative of locomotor diversity in our genus.","internal_url":"https://www.academia.edu/24659217/Thigh_and_leg_remains_of_Homo_naledi","translated_internal_url":"","created_at":"2016-04-22T06:29:20.207-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":44986372,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/44986372/thumbnails/1.jpg","file_name":"Abstract_Print_Marchi_et_al.pdf","download_url":"https://www.academia.edu/attachments/44986372/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Thigh_and_leg_remains_of_Homo_naledi.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/44986372/Abstract_Print_Marchi_et_al-libre.pdf?1461331801=\u0026response-content-disposition=attachment%3B+filename%3DThigh_and_leg_remains_of_Homo_naledi.pdf\u0026Expires=1733264552\u0026Signature=ZjTOebb4msFhw9eNSTFAXNl1Sw-xMOSi9yjRb14L-Wocuged-ZmjorsxijhLxdjv9Mg1e9223BvHvkJqJzqu8RPlHKxzIfVzfvXFFw4nJWhoRx-KE1~Hkkpnfi7TO5vwSDGYJ8bfV6L4vGFhx6XRRH37ZvD39ahqcrxEJ4B~soN1zOL7rdqZXKI~~LGanImybQVSUgbIp4hEXALawDPbgrqAmZ6wTP9FNy7p~Hh6u8pluQqcEc33f5H-lMozY2av6ozO-VrNUMaRYPPjExKC1WCEvqG8iHJ1nhMRYxLafMB7KlDtgyjKLgLjApgTdSjfO~Qm3929ogrx-UhE0mI~Lg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Thigh_and_leg_remains_of_Homo_naledi","translated_slug":"","page_count":2,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":44986372,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/44986372/thumbnails/1.jpg","file_name":"Abstract_Print_Marchi_et_al.pdf","download_url":"https://www.academia.edu/attachments/44986372/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Thigh_and_leg_remains_of_Homo_naledi.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/44986372/Abstract_Print_Marchi_et_al-libre.pdf?1461331801=\u0026response-content-disposition=attachment%3B+filename%3DThigh_and_leg_remains_of_Homo_naledi.pdf\u0026Expires=1733264552\u0026Signature=ZjTOebb4msFhw9eNSTFAXNl1Sw-xMOSi9yjRb14L-Wocuged-ZmjorsxijhLxdjv9Mg1e9223BvHvkJqJzqu8RPlHKxzIfVzfvXFFw4nJWhoRx-KE1~Hkkpnfi7TO5vwSDGYJ8bfV6L4vGFhx6XRRH37ZvD39ahqcrxEJ4B~soN1zOL7rdqZXKI~~LGanImybQVSUgbIp4hEXALawDPbgrqAmZ6wTP9FNy7p~Hh6u8pluQqcEc33f5H-lMozY2av6ozO-VrNUMaRYPPjExKC1WCEvqG8iHJ1nhMRYxLafMB7KlDtgyjKLgLjApgTdSjfO~Qm3929ogrx-UhE0mI~Lg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":66145,"name":"Hominin evolution","url":"https://www.academia.edu/Documents/in/Hominin_evolution"},{"id":85903,"name":"Tibia","url":"https://www.academia.edu/Documents/in/Tibia"},{"id":85904,"name":"Femur","url":"https://www.academia.edu/Documents/in/Femur"},{"id":366875,"name":"Fibulae","url":"https://www.academia.edu/Documents/in/Fibulae"},{"id":1737745,"name":"The Rising Star","url":"https://www.academia.edu/Documents/in/The_Rising_Star"},{"id":2104284,"name":"Homo naledi","url":"https://www.academia.edu/Documents/in/Homo_naledi"},{"id":2394726,"name":"Patella","url":"https://www.academia.edu/Documents/in/Patella"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="8431775"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/8431775/Can_distal_fibular_morphology_be_used_to_infer_Au_afarensis_locomotor_behavior"><img alt="Research paper thumbnail of Can distal fibular morphology be used to infer Au. afarensis locomotor behavior?" class="work-thumbnail" src="https://attachments.academia-assets.com/34821997/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/8431775/Can_distal_fibular_morphology_be_used_to_infer_Au_afarensis_locomotor_behavior">Can distal fibular morphology be used to infer Au. afarensis locomotor behavior?</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The fibula has rarely been considered in comparative morphological studies. The bones normally us...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The fibula has rarely been considered in comparative morphological studies. The bones normally used to investigate early hominin locomotor behavior are the largest bones of the hindlimb, femur and tibia. The reason for this choice is probably due to the relatively minor role of the fibula in carrying mechanical loads. However differences in morphology (and inferred function) of the fibula between human and non-human great apes, and within non-human great apes, have been noted in the past and related to differences in positional behavior. Recent research (Marchi, 2007; Marchi and Shaw, 2011) have pointed out the correlation present between diaphyseal structural properties of the fibula and locomotor behavior in living hominids (i.e. Pongo, Gorilla, Pan and Homo), and its possible application to inferring early hominin locomotor behavior. The problem with the method proposed in these studies is the extreme rarity of complete fibular diaphyses in the early hominin fossil record. However, distal fibular fragments are present in the fossil record. In particular, five distal fibulae of Australopithecus afaresis (i.e. AL 288-1at, AL 333-1a, AL 333-1b, AL 333-85, AL 333w-37) from the Hadar region of Ethiopia are available. Several morphological traits in the distal part of the fibula have been used in the past to infer locomotory adaptations and in particular the degree of arboreality in fossil hominins (Stern and Susman, 1983). However, the descriptions of these traits are often qualitatite. In this preliminary research articular measurements of the distal fibula of living hominids (Pongo, Gorilla, Pan and Homo, N = 107) are quantified. Besides articular area and breadth of the fibulotalar articular surfaces (i.e. proximal and distal), quantitative analysis is provided here of: 1. the angles formed by the fibulotalar articular surfaces with the longitudinal axis of the fibula; 2. the angle between the proximal portion of the fibulotalar articular surface and the subcutaneous triangular area of the fibula, which was hypothesized to be related to the degree of arboreality in great apes (Stern and Susman, 1983). Results show that the morphological characteristics of the distal fibula bear signals correlated with different locomotor behaviors particularly useful to distinguish between bipedal and non-bipedal hominids. The application of this method to the five distal Au. afarensis fibulae available shows how these morphological traits can be added to the ones normally investigated by palaeoanthropologists to better understand early hominin locomotory behavior.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="3d4e882c92058dc2b5ce6171fda921c9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":34821997,"asset_id":8431775,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/34821997/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="8431775"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="8431775"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 8431775; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=8431775]").text(description); $(".js-view-count[data-work-id=8431775]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 8431775; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='8431775']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 8431775, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "3d4e882c92058dc2b5ce6171fda921c9" } } $('.js-work-strip[data-work-id=8431775]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":8431775,"title":"Can distal fibular morphology be used to infer Au. afarensis locomotor behavior?","translated_title":"","metadata":{"abstract":"The fibula has rarely been considered in comparative morphological studies. The bones normally used to investigate early hominin locomotor behavior are the largest bones of the hindlimb, femur and tibia. The reason for this choice is probably due to the relatively minor role of the fibula in carrying mechanical loads. However differences in morphology (and inferred function) of the fibula between human and non-human great apes, and within non-human great apes, have been noted in the past and related to differences in positional behavior. Recent research (Marchi, 2007; Marchi and Shaw, 2011) have pointed out the correlation present between diaphyseal structural properties of the fibula and locomotor behavior in living hominids (i.e. Pongo, Gorilla, Pan and Homo), and its possible application to inferring early hominin locomotor behavior. The problem with the method proposed in these studies is the extreme rarity of complete fibular diaphyses in the early hominin fossil record. However, distal fibular fragments are present in the fossil record. In particular, five distal fibulae of Australopithecus afaresis (i.e. AL 288-1at, AL 333-1a, AL 333-1b, AL 333-85, AL 333w-37) from the Hadar region of Ethiopia are available. Several morphological traits in the distal part of the fibula have been used in the past to infer locomotory adaptations and in particular the degree of arboreality in fossil hominins (Stern and Susman, 1983). However, the descriptions of these traits are often qualitatite. In this preliminary research articular measurements of the distal fibula of living hominids (Pongo, Gorilla, Pan and Homo, N = 107) are quantified. Besides articular area and breadth of the fibulotalar articular surfaces (i.e. proximal and distal), quantitative analysis is provided here of: 1. the angles formed by the fibulotalar articular surfaces with the longitudinal axis of the fibula; 2. the angle between the proximal portion of the fibulotalar articular surface and the subcutaneous triangular area of the fibula, which was hypothesized to be related to the degree of arboreality in great apes (Stern and Susman, 1983). Results show that the morphological characteristics of the distal fibula bear signals correlated with different locomotor behaviors particularly useful to distinguish between bipedal and non-bipedal hominids. The application of this method to the five distal Au. afarensis fibulae available shows how these morphological traits can be added to the ones normally investigated by palaeoanthropologists to better understand early hominin locomotory behavior.","location":"Florence, Italy","more_info":"4th Annual meeting of the European Society for the study of Human Evolution","ai_title_tag":"Distal Fibular Morphology and Au. afarensis Locomotion","journal_name":"PESHE 3","conference_end_date":{"day":20,"month":9,"year":2014,"errors":{}},"conference_start_date":{"day":18,"month":9,"year":2014,"errors":{}}},"translated_abstract":"The fibula has rarely been considered in comparative morphological studies. The bones normally used to investigate early hominin locomotor behavior are the largest bones of the hindlimb, femur and tibia. The reason for this choice is probably due to the relatively minor role of the fibula in carrying mechanical loads. However differences in morphology (and inferred function) of the fibula between human and non-human great apes, and within non-human great apes, have been noted in the past and related to differences in positional behavior. Recent research (Marchi, 2007; Marchi and Shaw, 2011) have pointed out the correlation present between diaphyseal structural properties of the fibula and locomotor behavior in living hominids (i.e. Pongo, Gorilla, Pan and Homo), and its possible application to inferring early hominin locomotor behavior. The problem with the method proposed in these studies is the extreme rarity of complete fibular diaphyses in the early hominin fossil record. However, distal fibular fragments are present in the fossil record. In particular, five distal fibulae of Australopithecus afaresis (i.e. AL 288-1at, AL 333-1a, AL 333-1b, AL 333-85, AL 333w-37) from the Hadar region of Ethiopia are available. Several morphological traits in the distal part of the fibula have been used in the past to infer locomotory adaptations and in particular the degree of arboreality in fossil hominins (Stern and Susman, 1983). However, the descriptions of these traits are often qualitatite. In this preliminary research articular measurements of the distal fibula of living hominids (Pongo, Gorilla, Pan and Homo, N = 107) are quantified. Besides articular area and breadth of the fibulotalar articular surfaces (i.e. proximal and distal), quantitative analysis is provided here of: 1. the angles formed by the fibulotalar articular surfaces with the longitudinal axis of the fibula; 2. the angle between the proximal portion of the fibulotalar articular surface and the subcutaneous triangular area of the fibula, which was hypothesized to be related to the degree of arboreality in great apes (Stern and Susman, 1983). Results show that the morphological characteristics of the distal fibula bear signals correlated with different locomotor behaviors particularly useful to distinguish between bipedal and non-bipedal hominids. The application of this method to the five distal Au. afarensis fibulae available shows how these morphological traits can be added to the ones normally investigated by palaeoanthropologists to better understand early hominin locomotory behavior.","internal_url":"https://www.academia.edu/8431775/Can_distal_fibular_morphology_be_used_to_infer_Au_afarensis_locomotor_behavior","translated_internal_url":"","created_at":"2014-09-21T22:40:08.265-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":34821997,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/34821997/thumbnails/1.jpg","file_name":"Marchi__2014__PESHE_3_110.pdf","download_url":"https://www.academia.edu/attachments/34821997/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Can_distal_fibular_morphology_be_used_to.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/34821997/Marchi__2014__PESHE_3_110-libre.pdf?1411369743=\u0026response-content-disposition=attachment%3B+filename%3DCan_distal_fibular_morphology_be_used_to.pdf\u0026Expires=1733264552\u0026Signature=FwVLsbBUBW8bNEwroaLJL9OSQG3H4HClerMwA1ZUDpcAkBmenqF4JUFkOrt~8DLKkoiJpeJyivPcvGhTXKILyL3-n5DE2y4UvWG6~ADYRcAPvy2w2h8eBOGgpDKcpEGJyZCSKCYhGn3Zj85QsW0YF92QoATSNpqRaJ0s1IdWW7z~GTJXxdsIkcXFgnmONEmNHDGIzv-IRy190bMCZucOVbUeJrF1KQHdxf915zHSi4ok6nis0BSqlWK2gcppwwNF~DggOsVgl18sccxWG6WC5DAkLSVUwKXosoOWheM4tJ5-dUibMwnDcDhm0ni1fAnYh7Gs1XQKQ-~2n01H-h6Y0A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Can_distal_fibular_morphology_be_used_to_infer_Au_afarensis_locomotor_behavior","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":34821997,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/34821997/thumbnails/1.jpg","file_name":"Marchi__2014__PESHE_3_110.pdf","download_url":"https://www.academia.edu/attachments/34821997/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Can_distal_fibular_morphology_be_used_to.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/34821997/Marchi__2014__PESHE_3_110-libre.pdf?1411369743=\u0026response-content-disposition=attachment%3B+filename%3DCan_distal_fibular_morphology_be_used_to.pdf\u0026Expires=1733264552\u0026Signature=FwVLsbBUBW8bNEwroaLJL9OSQG3H4HClerMwA1ZUDpcAkBmenqF4JUFkOrt~8DLKkoiJpeJyivPcvGhTXKILyL3-n5DE2y4UvWG6~ADYRcAPvy2w2h8eBOGgpDKcpEGJyZCSKCYhGn3Zj85QsW0YF92QoATSNpqRaJ0s1IdWW7z~GTJXxdsIkcXFgnmONEmNHDGIzv-IRy190bMCZucOVbUeJrF1KQHdxf915zHSi4ok6nis0BSqlWK2gcppwwNF~DggOsVgl18sccxWG6WC5DAkLSVUwKXosoOWheM4tJ5-dUibMwnDcDhm0ni1fAnYh7Gs1XQKQ-~2n01H-h6Y0A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":156037,"name":"Australopithecus afarensis","url":"https://www.academia.edu/Documents/in/Australopithecus_afarensis"},{"id":473007,"name":"Early Hominins","url":"https://www.academia.edu/Documents/in/Early_Hominins"},{"id":1298116,"name":"Hominoid Locomotion","url":"https://www.academia.edu/Documents/in/Hominoid_Locomotion"},{"id":1299102,"name":"Arboreal Locomotion","url":"https://www.academia.edu/Documents/in/Arboreal_Locomotion"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="6166950"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/6166950/Investigating_hominin_tool_making_capabilities_using_micro_CT_scanning_of_metacarpal_bones"><img alt="Research paper thumbnail of Investigating hominin tool-making capabilities using micro CT scanning of metacarpal bones" class="work-thumbnail" src="https://attachments.academia-assets.com/33054163/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/6166950/Investigating_hominin_tool_making_capabilities_using_micro_CT_scanning_of_metacarpal_bones">Investigating hominin tool-making capabilities using micro CT scanning of metacarpal bones</a></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="79e292b0c34c663f29f50094a43743aa" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":33054163,"asset_id":6166950,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/33054163/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="6166950"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="6166950"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 6166950; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "79e292b0c34c663f29f50094a43743aa" } } $('.js-work-strip[data-work-id=6166950]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":6166950,"title":"Investigating hominin tool-making capabilities using micro CT scanning of metacarpal bones","translated_title":"","metadata":{"location":"NECSA, Pelindaba, South Africa","more_info":"1st South African Bi-annual National conference on Imaging with Radiation","grobid_abstract":"The discovery of hand bones stratigraphically associated with stone tools at Olduvai Gorge in the 1960 ignited debate about morphological correlates of hominin tool making and tool using. Retention of robust metacarpals was then argued to represent tool-making capabilities. Though stone tools dating as early as 2.6 million years have been discovered, robust hominin metacarpals only appear in fossil record after 1.8 million years. The debate then has been about which hominin was responsible for making the earliest stone tools and whether robusticity of metacarpals is a prerequisite for a stone-tool maker. The paucity of a full complement of hand bones dating prior to 600,000 years has limited inferences on stone-tool making. The recent discovery of a near complete hand of Australopithecus sediba has provided an opportunity to test the presumed link between metarcapal robusticity and tool making. The novel approach used in this paper consists of testing for metacarpal robusticity by comparing cross-sectional geometric properties of metacarpals across hominoid species (both human and non-human). 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Morphological adaptations favoring long distance flight may constrain the abilities of migrant birds to feed in certain habitats or substrates. Differences in habitat structure and prey availability between breeding and wintering environments may favor different foraging tactics in migrants and resident species. A relevant question is whether ecomorphological patterns of migrants differ from resident species in tropical and temperate environments. We used published and unpublished estimates of foraging data collected in the temperate zone and the Neotropics. Morphological differences between migrant and sedentary species from seven localities (both temperate and Neotropical) were determined by using eight external measurements taken from museum skins. Migrant species were smaller than tropical residents, but had relatively smaller wings and bills. However, migrants had longer wings, shorter tarsi and wider bills than temperate residents. The foraging behavior of migrants in the temperate zone was similar to their behavior when overwintering in the Neotropics. Migrants differed from temperate and tropical residents in foraging behavior. Our analyses found different ecomorphological configurations between migrants and residents. Notably, the regression plane for migrants was displaced relative to temperate or tropical residents. In other correlations the migrants showed significantly different ecomorphological patterns relative to residents of both temperate and tropical habitats. Our analyses suggest that migrants are \"between\" two worlds with respect to correlations of morphology and foraging behavior. We measured wet mass (MM), linear dimensions, and fiber length (FL) for each antebrachial muscle and calculated physiological cross sectional area (PCSA) for six strepsirrhines, six platyrrhines and seven catarrhines spanning nearly the entire primate body size range (from Galago to Gorilla). These variables were studied for each muscle and across muscles groups (flexors, extensors, and \"others\" -i.e., supinator, pronators, etc.) using RMA regression (alpha = 0.05). Total forearm (TFor) PCSA is tightly correlated with TFor MM across the whole sample and within each suborder and is slightly positively allometric across the whole sample and within strepsirrhines and catarrhines (but not platyrrhines). Similar correlations and allometry between MM and PCSA are found within the flexor and extensor compartments. However, FL is not highly correlated with total MM variables and instead correlates with locomotor patterns. Thus primate forearm muscles have relatively consistent (though slightly positively allometric) crossections, but vary according to FL, suggesting locomotor adaptations in stretch and flexibility, but not force production. Therefore the variation in the anatomy of the epicondyle likely relates to adaptations for mechanical advantage and not muscle force as has been previously hypothesized. One of the most active research areas in biology focuses on understanding how morphology maps onto function and performance, and how adaptations in these traits may allow lineages to diversify. Bats constitute an excellent system for investigating these connections because it is possible to explicitly quantify cranial traits and functional properties that are relevant to biting performance, and this group exhibits an outstanding diversity of dietary specializations within a relatively simple anatomical template. We present a comprehensive, quantitative dataset on the cranial morphology, muscle function and in vivo bite forces across several families of bats. We use these data in phylogenetic comparative analyses to determine how morphological diversity maps onto functional and performance diversity, and assess which and how morphological and functional traits are related to lineage diversification. Our results indicate a strong influence of body mass on the functional and performance diversity of the feeding apparatus in bats. Upon removing the effects of body size and phylogeny, disparity in some morphological variables exceeds the disparity in functional and performance traits. Similarly, changes in rates of character evolution seem to be more dynamic in morphological than in functional and performance traits. These results provide support for many-to-one mapping hypotheses of cranial anatomy to bite function, and could be linked to differences in the patterns of lineage diversification within bats.","conference_end_date":{"day":12,"month":7,"year":2013,"errors":{}},"conference_start_date":{"day":8,"month":7,"year":2013,"errors":{}},"grobid_abstract_attachment_id":33054064},"translated_abstract":null,"internal_url":"https://www.academia.edu/6166838/Correlation_of_forearm_muscle_architecture_and_locomotion_patterns_in_primates","translated_internal_url":"","created_at":"2014-02-21T23:03:27.235-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":125165,"coauthors_can_edit":true,"document_type":"other","co_author_tags":[],"downloadable_attachments":[{"id":33054064,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/33054064/thumbnails/1.jpg","file_name":"AnatRec_296__232_2013.pdf","download_url":"https://www.academia.edu/attachments/33054064/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Correlation_of_forearm_muscle_architectu.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/33054064/AnatRec_296__232_2013-libre.pdf?1393950020=\u0026response-content-disposition=attachment%3B+filename%3DCorrelation_of_forearm_muscle_architectu.pdf\u0026Expires=1733036087\u0026Signature=cmcHJT7-mpO2XQ9nMk~68mxjD~1zdgxSSsleC70TMLtCwPHfpUW7evnQkeWqf032yIYuORW0LMbkLa8ZJJtUlCmzeTk-kwR7XRRezURFdqNuAyUXY4goiMWWGLWOe~cfuh~72XBfj7H48-81z8SgbMJE28gUxp5RUzj5LYyWLDtVIvyMP-O3wedl7fVfwl-X~W5ryViZd6Ho2PhPL9WFwoJrDehf5oGPy5bLL4Cf7NARdvbYiFI8q6WEGSF46AfKIppW-EtN30jeyIMtG9IQlIMy0whdOcMwQakNLMJuYUbC8ojQG~VhkMfSbjEQjWIYP20IMwCR1lVQlPKp0w54Kw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Correlation_of_forearm_muscle_architecture_and_locomotion_patterns_in_primates","translated_slug":"","page_count":1,"language":"en","content_type":"Work","owner":{"id":125165,"first_name":"Damiano","middle_initials":null,"last_name":"Marchi","page_name":"DamianoMarchi","domain_name":"unipi","created_at":"2010-01-31T05:05:48.892-08:00","display_name":"Damiano Marchi","url":"https://unipi.academia.edu/DamianoMarchi"},"attachments":[{"id":33054064,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/33054064/thumbnails/1.jpg","file_name":"AnatRec_296__232_2013.pdf","download_url":"https://www.academia.edu/attachments/33054064/download_file?st=MTczMzI2MDk1Miw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Correlation_of_forearm_muscle_architectu.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/33054064/AnatRec_296__232_2013-libre.pdf?1393950020=\u0026response-content-disposition=attachment%3B+filename%3DCorrelation_of_forearm_muscle_architectu.pdf\u0026Expires=1733036087\u0026Signature=cmcHJT7-mpO2XQ9nMk~68mxjD~1zdgxSSsleC70TMLtCwPHfpUW7evnQkeWqf032yIYuORW0LMbkLa8ZJJtUlCmzeTk-kwR7XRRezURFdqNuAyUXY4goiMWWGLWOe~cfuh~72XBfj7H48-81z8SgbMJE28gUxp5RUzj5LYyWLDtVIvyMP-O3wedl7fVfwl-X~W5ryViZd6Ho2PhPL9WFwoJrDehf5oGPy5bLL4Cf7NARdvbYiFI8q6WEGSF46AfKIppW-EtN30jeyIMtG9IQlIMy0whdOcMwQakNLMJuYUbC8ojQG~VhkMfSbjEQjWIYP20IMwCR1lVQlPKp0w54Kw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":1299102,"name":"Arboreal Locomotion","url":"https://www.academia.edu/Documents/in/Arboreal_Locomotion"},{"id":1299177,"name":"Terrestrial Locomotion","url":"https://www.academia.edu/Documents/in/Terrestrial_Locomotion"}],"urls":[]}, dispatcherData: dispatcherData }); 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The structure morphology of bones is closely associated to their function, but, a consensus on the correlation between bone structure and function has not yet been achieved. The aim of this study is to provide for the first an integrative approach to the study of bone structure. We propose to integrate the study of shape of the bone (i.e., the geometric morphometrics approach) with the study of biomechanics of the bone (i.e., the cross-sectional geometry approach) to understand the morpho-functional variation of the femur. The geometric morphometrics analysis allows to quantify the geometric variation of the anatomical structures by using Cartesian coordinates. The cross-sectional geometric analysis, based on the geometric distribution of bone in a cross-section, provides information on the direction and magnitude of the forces to which the bone is subjected during postural dynamics. The analysis was computed on a sample of CT-scan cross-section of the femur at midshaft. This analysis shows that the direction of the major load at this level is correlated with anterolateral and postero-medial variations of the section, in agreement with the mechanical loading of the femur at midshaft. Because of the small sample size these results should be considered as preliminary. 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="6166429"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/6166429/Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale"><img alt="Research paper thumbnail of Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale." class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/6166429/Un_approccio_biomeccanico_alla_ricostruzione_delle_strategie_di_sussistenza_delle_popolazioni_neolitiche_della_Liguria_occidentale">Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale.</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferior...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri (LIG). Il metodo di indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un livello di robustezza non dissimile da quello dei cacciatori paleolitici e significativamente più elevato rispetto alle popolazioni contemporanee, cosa che suggerisce un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione suggerisce che queste attività di sussistenza fossero radicalmente diverse nei due sessi. Infatti, i maschi presentano una elevata lateralizzazione, associabile all’uso delle asce in pietra verde così frequenti nei livelli neolitici. Al contrario, le femmine presentano un livello di lateralizzazione significativamente più basso del normale, associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. Per quanto riguarda l’arto inferiore, i LIG non mostrano la riduzione nella robustezza dell’arto inferiore che è invece caratteristica del campione tardo neolitico utilizzato come confronto. I LIG risultano invece più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, i maschi LIG risultano molto più robusti delle femmine suggerendo una marcata differenziazione dei ruoli tra i sessi. In definitiva, i risultati dell’analisi della robustezza meccanica e degli indici di forma diafisaria dell’arto inferiore suggeriscono che i LIG fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che i LIG conducessero attività di sussistenza prevalentemente pastorali.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="6166429"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span><span id="work-strip-rankings-button-container"></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="6166429"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 6166429; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=6166429]").text(description); $(".js-view-count[data-work-id=6166429]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 6166429; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='6166429']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 6166429, container: "", }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-f77ea15d77ce96025a6048a514272ad8becbad23c641fc2b3bd6e24ca6ff1932.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (false){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=6166429]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":6166429,"title":"Un approccio biomeccanico alla ricostruzione delle strategie di sussistenza delle popolazioni neolitiche della Liguria occidentale.","translated_title":"","metadata":{"abstract":"In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri (LIG). Il metodo di indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un livello di robustezza non dissimile da quello dei cacciatori paleolitici e significativamente più elevato rispetto alle popolazioni contemporanee, cosa che suggerisce un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione suggerisce che queste attività di sussistenza fossero radicalmente diverse nei due sessi. Infatti, i maschi presentano una elevata lateralizzazione, associabile all’uso delle asce in pietra verde così frequenti nei livelli neolitici. Al contrario, le femmine presentano un livello di lateralizzazione significativamente più basso del normale, associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. Per quanto riguarda l’arto inferiore, i LIG non mostrano la riduzione nella robustezza dell’arto inferiore che è invece caratteristica del campione tardo neolitico utilizzato come confronto. I LIG risultano invece più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, i maschi LIG risultano molto più robusti delle femmine suggerendo una marcata differenziazione dei ruoli tra i sessi. In definitiva, i risultati dell’analisi della robustezza meccanica e degli indici di forma diafisaria dell’arto inferiore suggeriscono che i LIG fossero una popolazione molto mobile su un territorio accidentato e forniscono supporto all’ipotesi basata su evidenze archeologiche che i LIG conducessero attività di sussistenza prevalentemente pastorali.","location":"Finale Ligure Borgo (SV), Italy","more_info":"\u0002\u0003Il pieno sviluppo del Neolitico in Italia, Congresso ","conference_end_date":{"day":10,"month":6,"year":2009,"errors":{}},"conference_start_date":{"day":8,"month":6,"year":2009,"errors":{}}},"translated_abstract":"In questo studio, le caratteristiche strutturali dell’arto superiore (omero) e di quello inferiore (femore e tibia) sono state analizzate per ricostruire le strategie di sussitenza delle popolazione neolitiche liguri (LIG). Il metodo di indagine utilizzato consiste nello studio della geometria delle sezione a metá diafisi dell’osso. I risultati riguardanti l’omero evidenziano un livello di robustezza non dissimile da quello dei cacciatori paleolitici e significativamente più elevato rispetto alle popolazioni contemporanee, cosa che suggerisce un uso frequente dell’arto superiore nelle attività di sussistenza. Lo studio della lateralizzazione suggerisce che queste attività di sussistenza fossero radicalmente diverse nei due sessi. Infatti, i maschi presentano una elevata lateralizzazione, associabile all’uso delle asce in pietra verde così frequenti nei livelli neolitici. Al contrario, le femmine presentano un livello di lateralizzazione significativamente più basso del normale, associabile ad un frequente uso di macine a due mani per la macinatura dei cereali. Per quanto riguarda l’arto inferiore, i LIG non mostrano la riduzione nella robustezza dell’arto inferiore che è invece caratteristica del campione tardo neolitico utilizzato come confronto. I LIG risultano invece più simili, sia nei livelli di robustezza che negli indici di forma diafisaria, alle popolazioni di confronto altamente mobili del Paleolitico Superiore Recente. Inoltre, i maschi LIG risultano molto più robusti delle femmine suggerendo una marcata differenziazione dei ruoli tra i sessi. 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