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href="https://www.academia.edu/Documents/in/Geomatic_Engineering"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{&quot;color&quot;:&quot;gray&quot;,&quot;children&quot;:[&quot;Geomatic Engineering&quot;]}" data-trace="false" data-dom-id="Pill-react-component-8a79e6fd-5540-4f97-81b4-9e6fed662bfa"></div> <div id="Pill-react-component-8a79e6fd-5540-4f97-81b4-9e6fed662bfa"></div> </a><a data-click-track="profile-user-info-expand-research-interests" data-has-card-for-ri-list="41682648" href="https://www.academia.edu/Documents/in/Forest_Management"><div class="js-react-on-rails-component" style="display:none" data-component-name="Pill" data-props="{&quot;color&quot;:&quot;gray&quot;,&quot;children&quot;:[&quot;Forest Management&quot;]}" data-trace="false" data-dom-id="Pill-react-component-3ef88475-2ff0-4a25-afc0-5ab65c5c66f6"></div> <div id="Pill-react-component-3ef88475-2ff0-4a25-afc0-5ab65c5c66f6"></div> </a><a 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id="Pill-react-component-b63a9123-970a-4a2b-85bc-db9fcd255ed0"></div> </a></div></div></div></div><div class="right-panel-container"><div class="user-content-wrapper"><div class="uploads-container" id="social-redesign-work-container"><div class="upload-header"><h2 class="ds2-5-heading-sans-serif-xs">Uploads</h2></div><div class="documents-container backbone-social-profile-documents" style="width: 100%;"><div class="u-taCenter"></div><div class="profile--tab_content_container js-tab-pane tab-pane active" id="all"><div class="profile--tab_heading_container js-section-heading" data-section="Papers" id="Papers"><h3 class="profile--tab_heading_container">Papers by John Nason</h3></div><div class="js-work-strip profile--work_container" data-work-id="100056203"><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/100056203/AFLP_data_of_Lythrum_salicaria"><img alt="Research paper thumbnail of AFLP data of Lythrum salicaria" 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/100056203/AFLP_data_of_Lythrum_salicaria">AFLP data of Lythrum salicaria</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 class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="100056203"><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 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container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 100056203, 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" } } $('.js-work-strip[data-work-id=100056203]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":100056203,"title":"AFLP data of Lythrum 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Species","url":"https://www.academia.edu/Documents/in/Invasive_Species"},{"id":510989,"name":"AFLP","url":"https://www.academia.edu/Documents/in/AFLP"},{"id":547589,"name":"Quantitative Trait Loci","url":"https://www.academia.edu/Documents/in/Quantitative_Trait_Loci"},{"id":577933,"name":"Genetic variation","url":"https://www.academia.edu/Documents/in/Genetic_variation"},{"id":748344,"name":"Lythrum Salicaria","url":"https://www.academia.edu/Documents/in/Lythrum_Salicaria"}],"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="100055950"><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/100055950/Data_from_Comparison_of_quantitative_and_molecular_genetic_variation_of_native_vs_invasive_populations_of_purple_loosestrife_Lythrum_salicaria_L_Lythraceae_"><img alt="Research paper thumbnail of Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)" 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/100055950/Data_from_Comparison_of_quantitative_and_molecular_genetic_variation_of_native_vs_invasive_populations_of_purple_loosestrife_Lythrum_salicaria_L_Lythraceae_">Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Study of adaptive evolutionary changes in populations of invasive species can be advanced through...</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">Study of adaptive evolutionary changes in populations of invasive species can be advanced through the joint application of quantitative and population genetic methods. Using purple loosestrife as a model system, we investigated the relative roles of natural selection, genetic drift, ...</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="100055950"><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="100055950"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 100055950; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=100055950]").text(description); $(".js-view-count[data-work-id=100055950]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 100055950; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='100055950']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 100055950, 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" } } $('.js-work-strip[data-work-id=100055950]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":100055950,"title":"Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)","translated_title":"","metadata":{"abstract":"Study of adaptive evolutionary changes in populations of invasive species can be advanced through the joint application of quantitative and population genetic methods. 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Using purple loosestrife as a model system, we investigated the relative roles of natural selection, genetic drift, ...","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[],"research_interests":[],"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="92805533"><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/92805533/Population_Structure_and_Genetic_Diversity_of_the_Boll_Weevil_Coleoptera_Curculionidae_on_Gossypium_in_North_America"><img alt="Research paper thumbnail of Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America" class="work-thumbnail" src="https://attachments.academia-assets.com/95717002/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/92805533/Population_Structure_and_Genetic_Diversity_of_the_Boll_Weevil_Coleoptera_Curculionidae_on_Gossypium_in_North_America">Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a de...</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">Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity in Mexico on wild and cultivated cotton hosts (genus Gossypium) is poorly understood. Past studies using morphology, host use, and distribution records suggest that A.grandis grandis comprises three forms with host-associated characteristics: the southeastern form (from domesticated Gossypium hirsutum L., southeastern United States and northeastern Mexico), the thurberia form (from Gossypium thurberi Todaro, Arizona and northwestern Mexico), and the Mexican form (from multiple Gossypium species and other malvaceous plant genera in the remainder of Mexico and Central America). However, the phylogenetic relationships, host preferences, and distributions of these forms are not completely understood. An alternative hypothesis of an eastern and western form of the boll weevil is suggested by the sus...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="db100d12b59c49215670089229230ebe" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:95717002,&quot;asset_id&quot;:92805533,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/95717002/download_file?st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="92805533"><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="92805533"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 92805533; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=92805533]").text(description); $(".js-view-count[data-work-id=92805533]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 92805533; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='92805533']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 92805533, 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: "db100d12b59c49215670089229230ebe" } } $('.js-work-strip[data-work-id=92805533]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":92805533,"title":"Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America","translated_title":"","metadata":{"abstract":"Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity in Mexico on wild and cultivated cotton hosts (genus Gossypium) is poorly understood. Past studies using morphology, host use, and distribution records suggest that A.grandis grandis comprises three forms with host-associated characteristics: the southeastern form (from domesticated Gossypium hirsutum L., southeastern United States and northeastern Mexico), the thurberia form (from Gossypium thurberi Todaro, Arizona and northwestern Mexico), and the Mexican form (from multiple Gossypium species and other malvaceous plant genera in the remainder of Mexico and Central America). However, the phylogenetic relationships, host preferences, and distributions of these forms are not completely understood. An alternative hypothesis of an eastern and western form of the boll weevil is suggested by the sus...","publisher":"Iowa State University Digital Repository","publication_date":{"day":null,"month":null,"year":2012,"errors":{}}},"translated_abstract":"Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity in Mexico on wild and cultivated cotton hosts (genus Gossypium) is poorly understood. 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Past studies using morphology, host use, and distribution records suggest that A.grandis grandis comprises three forms with host-associated characteristics: the southeastern form (from domesticated Gossypium hirsutum L., southeastern United States and northeastern Mexico), the thurberia form (from Gossypium thurberi Todaro, Arizona and northwestern Mexico), and the Mexican form (from multiple Gossypium species and other malvaceous plant genera in the remainder of Mexico and Central America). However, the phylogenetic relationships, host preferences, and distributions of these forms are not completely understood. 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In this paper, we consider three typical sources of scoring errors capable of biasing biological conclusions: stuttering, large-allele dropout and null alleles. We describe methods to detect errors and propose conventions to mitigate scoring errors and report error rates in studies of wild populations. Finally, we discuss potential bias in ecological or evolutionary conclusions based on data sets containing these scoring errors.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="ddc4871ce49e99460ac0d65132783766" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:86564549,&quot;asset_id&quot;:80055739,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/86564549/download_file?st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="80055739"><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="80055739"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 80055739; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=80055739]").text(description); $(".js-view-count[data-work-id=80055739]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 80055739; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='80055739']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 80055739, 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: "ddc4871ce49e99460ac0d65132783766" } } $('.js-work-strip[data-work-id=80055739]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":80055739,"title":"Mitigating scoring errors in microsatellite data from wild populations","translated_title":"","metadata":{"publisher":"Wiley-Blackwell","ai_title_tag":"Reducing Scoring Errors in Microsatellite Data of Wild Populations","grobid_abstract":"Microsatellite data are widely used to test ecological and evolutionary hypotheses in wild populations. 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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="73755085"><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/73755085/Extraordinarily_Precise_Nematode_Sex_Ratios_Adaptive_Responses_to_Vanishingly_Rare_Mating_Options"><img alt="Research paper thumbnail of Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options" class="work-thumbnail" src="https://attachments.academia-assets.com/82152140/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/73755085/Extraordinarily_Precise_Nematode_Sex_Ratios_Adaptive_Responses_to_Vanishingly_Rare_Mating_Options">Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options</a></div><div class="wp-workCard_item"><span>bioRxiv</span><span>, 2021</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Sex ratio theory predicts both mean sex ratio and variance under a range of population structures...</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">Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). In further contrast with their hosts, variances in nematode sex ratios are also consistently precise (significantly less than binomia...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6916d7460973c889504a050011497f84" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152140,&quot;asset_id&quot;:73755085,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152140/download_file?st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755085"><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="73755085"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755085; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755085]").text(description); $(".js-view-count[data-work-id=73755085]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755085; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755085']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755085, 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: "6916d7460973c889504a050011497f84" } } $('.js-work-strip[data-work-id=73755085]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755085,"title":"Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options","translated_title":"","metadata":{"abstract":"Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). In further contrast with their hosts, variances in nematode sex ratios are also consistently precise (significantly less than binomia...","publication_date":{"day":null,"month":null,"year":2021,"errors":{}},"publication_name":"bioRxiv"},"translated_abstract":"Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. 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Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). 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These community-level associations have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because identifying species interacting with focal mutualists and assessing their associated fitness benefits and costs is difficult, especially over space and through time. Here, we focus on a community comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) commensals/antagonists, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field experiments, we identified that all NPFWs are targets for infection by this nematode. Further, this infection can impact NPFWs more severely than either mutualistic partner, sugg...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="712805df8756d3e56fba0c6b9810f3ff" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152139,&quot;asset_id&quot;:73755084,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152139/download_file?st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755084"><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="73755084"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755084; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755084]").text(description); $(".js-view-count[data-work-id=73755084]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755084; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755084']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755084, 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: "712805df8756d3e56fba0c6b9810f3ff" } } $('.js-work-strip[data-work-id=73755084]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755084,"title":"The enemy of my enemy is my friend: Nematode infection of pollinating and non-pollinating fig wasps has net benefits for the fig-fig wasp pollination mutualism","translated_title":"","metadata":{"abstract":"Mutualistic associations between species pairs are ubiquitous in nature but are also components of broader organismal community networks. These community-level associations have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because identifying species interacting with focal mutualists and assessing their associated fitness benefits and costs is difficult, especially over space and through time. Here, we focus on a community comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) commensals/antagonists, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field experiments, we identified that all NPFWs are targets for infection by this nematode. 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These community-level associations have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because identifying species interacting with focal mutualists and assessing their associated fitness benefits and costs is difficult, especially over space and through time. Here, we focus on a community comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) commensals/antagonists, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field experiments, we identified that all NPFWs are targets for infection by this nematode. 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Although examples of mutualism are ubiquitous in nature, the ecology, evolution, and stability of mutualism has rarely been studied in the broader, multispecies community context in which they occur. The pollination mutualism between figs and fig wasps provides an excellent model system for investigating interactions between obligate mutualists and antagonists. Compared to the community of non-pollinating fig wasps that develop within figs inflorescences at the expense of fig seeds and pollinators, consequences of interactions between female pollinating wasps and their host-specialist nematode parasites is much less well understood. Here we focus on a tri-partite system comprised of a fig (Ficus petiolaris), pollinating wasp (Pegoscapus sp.), and nematode (Parasitodiplogaster sp.), investigating geographical variation in the incidence of attack and mechanisms through which nematodes may limit the fitness of their wasp hosts at successive life history stages. Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. The result that nematode infection appears to be largely benign-and the unexpected finding that nematodes frequently infect non-pollinating wasps-highlight gaps in our knowledge of pollinator-Parasitodiplogaster interactions and suggest previously unappreciated ways in which this nematode may influence fig and pollinator fitness, mutualism persistence, and non-pollinator community dynamics.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b8125c0f121feaaa2354da9e3f2fdc1f" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152141,&quot;asset_id&quot;:73755082,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152141/download_file?st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755082"><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="73755082"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755082; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755082]").text(description); $(".js-view-count[data-work-id=73755082]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755082; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755082']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755082, 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: "b8125c0f121feaaa2354da9e3f2fdc1f" } } $('.js-work-strip[data-work-id=73755082]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755082,"title":"Figs, pollinators, and parasites: A longitudinal study of the effects of nematode infection on fig wasp fitness","translated_title":"","metadata":{"publisher":"Elsevier BV","ai_title_tag":"Impact of Nematode Infection on Fig Wasp Fitness","grobid_abstract":"Mutualisms are interactions between two species in which the fitnesses of both symbionts benefit from the relationship. 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Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. 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Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. 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Sappington, Kyung Seok Kim, Norman B</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 class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="73755081"><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="73755081"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755081; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755081]").text(description); $(".js-view-count[data-work-id=73755081]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755081; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755081']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755081, 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" } } $('.js-work-strip[data-work-id=73755081]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755081,"title":"Adam P. 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Accessions During Caged Germplasm Regeneration" class="work-thumbnail" src="https://attachments.academia-assets.com/82151947/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/73754957/Measuring_the_Effectiveness_of_Isolation_of_Brassica_napus_L_Accessions_During_Caged_Germplasm_Regeneration">Measuring the Effectiveness of Isolation of Brassica napus L. Accessions During Caged Germplasm Regeneration</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Gene flow, which is the successful movement of genes among populations by mating or migration 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">Gene flow, which is the successful movement of genes among populations by mating or migration of seeds or other propagules, has gained much interest in agriculture in recent years because of the widescale adoption of transgenic crops and concerns over transgene escape into the wild ( James 2004; Messeguer 2003; Stewart et al. 2003). Brassica napus (rapeseed), together with maize and sugar beet, have been identified among the species for which cross-pollination and transgene escape are concerns (Treu and Emberlin 2000). Disciplines Ecology and Evolutionary Biology | Genetics Comments This article is from PGR Newsletter issue no. 154 (2008): 14. Rights Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted. This article is available at Iowa State University Digital Repository: <a href="https://lib.dr.iastate.edu/eeob_ag_pubs/77" rel="nofollow">https://lib.dr.iastate.edu/eeob_ag_pubs/77</a> 1G&amp;#39;1~15 Pin Genetic Resources Na Article Latest (Fr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c238c05aa160d3a30e81a14beb0d50bc" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82151947,&quot;asset_id&quot;:73754957,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82151947/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="73754957"><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="73754957"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73754957; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73754957]").text(description); $(".js-view-count[data-work-id=73754957]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73754957; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73754957']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73754957, 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: "c238c05aa160d3a30e81a14beb0d50bc" } } $('.js-work-strip[data-work-id=73754957]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73754957,"title":"Measuring the Effectiveness of Isolation of Brassica napus L. 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These interaction networks have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because characterizing the impacts of species interacting with focal mutualists is often difficult. How is the fitness of mutualists impacted by the co-occurring interactive network of community associates? We investigate this context using a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field observations we characterize the ecological roles of these mutualist-associated organisms to identify key antagonists. We then investigated how pote...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5ef971d6e6086429a4541a96c2c204db" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82151854,&quot;asset_id&quot;:73754879,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82151854/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="73754879"><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="73754879"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73754879; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73754879]").text(description); $(".js-view-count[data-work-id=73754879]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73754879; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73754879']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73754879, 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: "5ef971d6e6086429a4541a96c2c204db" } } $('.js-work-strip[data-work-id=73754879]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73754879,"title":"Differential effects of nematode infection on pollinating and non-pollinating fig wasps: can shared antagonism provide net benefits to a mutualism?","translated_title":"","metadata":{"abstract":"Species pairs that form mutualistic associations are also components of broader organismal community networks. 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We then investigated how pote...","publisher":"The Journal of animal ecology","publication_date":{"day":null,"month":null,"year":2021,"errors":{}},"publication_name":"The Journal of animal ecology"},"translated_abstract":"Species pairs that form mutualistic associations are also components of broader organismal community networks. These interaction networks have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because characterizing the impacts of species interacting with focal mutualists is often difficult. How is the fitness of mutualists impacted by the co-occurring interactive network of community associates? We investigate this context using a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field observations we characterize the ecological roles of these mutualist-associated organisms to identify key antagonists. We then investigated how pote...","internal_url":"https://www.academia.edu/73754879/Differential_effects_of_nematode_infection_on_pollinating_and_non_pollinating_fig_wasps_can_shared_antagonism_provide_net_benefits_to_a_mutualism","translated_internal_url":"","created_at":"2022-03-14T09:32:31.364-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":41682648,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":82151854,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/82151854/thumbnails/1.jpg","file_name":"viewcontent.pdf","download_url":"https://www.academia.edu/attachments/82151854/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Differential_effects_of_nematode_infecti.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/82151854/viewcontent-libre.pdf?1647275723=\u0026response-content-disposition=attachment%3B+filename%3DDifferential_effects_of_nematode_infecti.pdf\u0026Expires=1734172621\u0026Signature=YkLYnt~OeEap164kutR-xv9fPrUVrm7LbuYivXrPeoS7Fj-miNVrBqNKsvS671doy4zjOEI6HgFAZpqtlTf0XP0wMQVc2Zkshajp-o1kdMyA3QCDezBiWWzGV8ejmNs6Wd9lK-Gq8bhLiiAlWDmpmyMc9Tvv77p0cB9WepOzoiIvOW4OZJ~AguVLX23cogWgR63M97Ae3FgZizi3aGr2z4ybXz~A1HPqd3cpR4X4wbjmqWV6YG0DeiumnlDyZClROenHgFJZkD45pv33mmooc5lzdWT7rlTvyhvFxCWca-1mBRcuYGNolsy9Xru9k4Sj2NK5thoG43MHTqCxst2q4g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Differential_effects_of_nematode_infection_on_pollinating_and_non_pollinating_fig_wasps_can_shared_antagonism_provide_net_benefits_to_a_mutualism","translated_slug":"","page_count":15,"language":"en","content_type":"Work","summary":"Species pairs that form mutualistic associations are also components of broader organismal community networks. These interaction networks have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because characterizing the impacts of species interacting with focal mutualists is often difficult. How is the fitness of mutualists impacted by the co-occurring interactive network of community associates? We investigate this context using a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field observations we characterize the ecological roles of these mutualist-associated organisms to identify key antagonists. We then investigated how pote...","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":82151854,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/82151854/thumbnails/1.jpg","file_name":"viewcontent.pdf","download_url":"https://www.academia.edu/attachments/82151854/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Differential_effects_of_nematode_infecti.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/82151854/viewcontent-libre.pdf?1647275723=\u0026response-content-disposition=attachment%3B+filename%3DDifferential_effects_of_nematode_infecti.pdf\u0026Expires=1734172621\u0026Signature=YkLYnt~OeEap164kutR-xv9fPrUVrm7LbuYivXrPeoS7Fj-miNVrBqNKsvS671doy4zjOEI6HgFAZpqtlTf0XP0wMQVc2Zkshajp-o1kdMyA3QCDezBiWWzGV8ejmNs6Wd9lK-Gq8bhLiiAlWDmpmyMc9Tvv77p0cB9WepOzoiIvOW4OZJ~AguVLX23cogWgR63M97Ae3FgZizi3aGr2z4ybXz~A1HPqd3cpR4X4wbjmqWV6YG0DeiumnlDyZClROenHgFJZkD45pv33mmooc5lzdWT7rlTvyhvFxCWca-1mBRcuYGNolsy9Xru9k4Sj2NK5thoG43MHTqCxst2q4g__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"},{"id":82151853,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/82151853/thumbnails/1.jpg","file_name":"viewcontent.pdf","download_url":"https://www.academia.edu/attachments/82151853/download_file","bulk_download_file_name":"Differential_effects_of_nematode_infecti.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/82151853/viewcontent-libre.pdf?1647275722=\u0026response-content-disposition=attachment%3B+filename%3DDifferential_effects_of_nematode_infecti.pdf\u0026Expires=1734172621\u0026Signature=dhj4ARJR2nTr3mOdBJVPVUb2tHwVLBTC8SI~j6M5if-IR9MFg9xgcYp4aUD3JHbu3fNRVQT4HX3UcQz4pACZvSFBMX8scvVLfj0gcEqkQ2ey2Y6GhpTapn63OM4-5px1cGp4okZCQKakv1jsd5VFoxDIs8bTF9kuvyV2eXLq5P4ymzHDtc2-Ip2OYqfFA-e4R6xZMMgWe60s~2iwAYZb0zeIiAZ8dmN7xuPTA18fZBzKM3Q-b9M7H4ObrRfJNMm~wAfwrPHyCA1OEsJos13eEc219l-8FRct9Hw1XCg208kOf52WqFJzkPC7wloclYbbpd6JJ9zqLAm9WAkaTk3qKg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":14483,"name":"Animal Ecology","url":"https://www.academia.edu/Documents/in/Animal_Ecology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":58054,"name":"Environmental Sciences","url":"https://www.academia.edu/Documents/in/Environmental_Sciences"}],"urls":[{"id":18505628,"url":"https://lib.dr.iastate.edu/cgi/viewcontent.cgi?article=1469\u0026context=eeob_ag_pubs"}]}, dispatcherData: dispatcherData }); 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In nursery pollination mutualisms, pollinators reproduce within the inflorescence they pollinate, with benefits and costs being measured in the numbers of pollinator offspring and seeds produced. This type of mutualism is also typically exploited by seed-consuming nonpollinators that obtain resources from plants without providing pollination services. Theory predicts that the rate at which pollen-bearing \"foundresses\" visit a plant will strongly affect the plant's production of pollinator offspring, non-pollinator offspring, and seeds. Spatially aggregated plants are predicted to have high rates of foundress visitation, increasing pollinator and seed production, and decreasing non-pollinator production; very high foundress visitation may also decrease seed production indirectly through the production of pollinators. Working with a nursery mutualism comprised of interactions to benefits and costs: 1) foundress density increases with host-tree connectivity, 2) pollinator production increases with foundress density, and 3) nonpollinator production and 4) seed production decrease with pollinator production. We also directly test how tree connectivity affects non-pollinator production. We find strong support for our four hypotheses, and we conclude that tree connectivity is a key driver of foundress visitation, thereby strongly affecting spatial distributions in the F. petiolaris community. We also find that foundress visitation decreases at the northernmost edge of the F. petiolaris range. Finally, we find species-specific effects of tree connectivity on non-pollinators to be strongly correlated with previously estimated non-pollinator dispersal abilities. We conclude that plant connectivity is highly important for predicting plant-pollinator-exploiter dynamics, and discuss the implications of our results for species coexistence and adaptation.","publication_name":"Oikos"},"translated_abstract":null,"internal_url":"https://www.academia.edu/69436104/Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps","translated_internal_url":"","created_at":"2022-01-25T10:08:34.007-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":41682648,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":79535585,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/79535585/thumbnails/1.jpg","file_name":"Duthie_et_al_2016_Oikos.pdf","download_url":"https://www.academia.edu/attachments/79535585/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Plant_connectivity_underlies_plant_polli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/79535585/Duthie_et_al_2016_Oikos-libre.pdf?1643137931=\u0026response-content-disposition=attachment%3B+filename%3DPlant_connectivity_underlies_plant_polli.pdf\u0026Expires=1734172621\u0026Signature=eCfkZJs3GZcK9Rmp1au2NxZq0Zy~KFykSjMn3Q93W3XgdPhKlUNwjuAk3u8elrf3a26GjWCGNPjonjQqjrZbg3C~~Q3S9eI0G4ynIGJ6Nra4ZI6bu3V4bMUSEFI0ZztxmJt9bZ9Kkz-wcEjgwmSQ-D0kgjVIU~NTa7B0lHNFWQMheUO5FHsiovm~pB9Hrw7lSQpdOc3XG3pUNDeDZWXwlCU2LVq2rNpEkt5Epcq7bH-xa2KnK1HM5MG4l5Sp2-ltwKcgMAcVziM6jafadY3cvWzj2JNUAcaGh5M2QVvyu0zF7N8HgzGeJ4aVBx~wXVdkgp9E1PVDC7zooegvgh1XPA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps","translated_slug":"","page_count":32,"language":"en","content_type":"Work","summary":null,"owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":79535585,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/79535585/thumbnails/1.jpg","file_name":"Duthie_et_al_2016_Oikos.pdf","download_url":"https://www.academia.edu/attachments/79535585/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Plant_connectivity_underlies_plant_polli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/79535585/Duthie_et_al_2016_Oikos-libre.pdf?1643137931=\u0026response-content-disposition=attachment%3B+filename%3DPlant_connectivity_underlies_plant_polli.pdf\u0026Expires=1734172621\u0026Signature=eCfkZJs3GZcK9Rmp1au2NxZq0Zy~KFykSjMn3Q93W3XgdPhKlUNwjuAk3u8elrf3a26GjWCGNPjonjQqjrZbg3C~~Q3S9eI0G4ynIGJ6Nra4ZI6bu3V4bMUSEFI0ZztxmJt9bZ9Kkz-wcEjgwmSQ-D0kgjVIU~NTa7B0lHNFWQMheUO5FHsiovm~pB9Hrw7lSQpdOc3XG3pUNDeDZWXwlCU2LVq2rNpEkt5Epcq7bH-xa2KnK1HM5MG4l5Sp2-ltwKcgMAcVziM6jafadY3cvWzj2JNUAcaGh5M2QVvyu0zF7N8HgzGeJ4aVBx~wXVdkgp9E1PVDC7zooegvgh1XPA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology"},{"id":156991,"name":"Oikos","url":"https://www.academia.edu/Documents/in/Oikos"}],"urls":[{"id":16890365,"url":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Foik.02905"}]}, 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="61821584"><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/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_"><img alt="Research paper thumbnail of Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)" class="work-thumbnail" src="https://attachments.academia-assets.com/74760408/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/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_">Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)</a></div><div class="wp-workCard_item"><span>Heredity</span><span>, 2003</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tr...</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">Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright&#39;s fixation index, spatial autocorrelation statistics (Moran&#39;s I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran&#39;s I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="82048dc14d4c9d3034c0d1b425cbf6db" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:74760408,&quot;asset_id&quot;:61821584,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="61821584"><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="61821584"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 61821584; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=61821584]").text(description); $(".js-view-count[data-work-id=61821584]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 61821584; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='61821584']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 61821584, 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: "82048dc14d4c9d3034c0d1b425cbf6db" } } $('.js-work-strip[data-work-id=61821584]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":61821584,"title":"Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)","translated_title":"","metadata":{"publisher":"Springer Nature","ai_title_tag":"Genetic Structure of Cinnamomum insularimontanum Across Age Classes","grobid_abstract":"Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright's fixation index, spatial autocorrelation statistics (Moran's I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran's I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.","publication_date":{"day":null,"month":null,"year":2003,"errors":{}},"publication_name":"Heredity","grobid_abstract_attachment_id":74760408},"translated_abstract":null,"internal_url":"https://www.academia.edu/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_","translated_internal_url":"","created_at":"2021-11-16T21:19:54.315-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":41682648,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":74760408,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/74760408/thumbnails/1.jpg","file_name":"6800187.pdf","download_url":"https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Temporal_aspects_of_the_fine_scale_genet.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/74760408/6800187-libre.pdf?1637128866=\u0026response-content-disposition=attachment%3B+filename%3DTemporal_aspects_of_the_fine_scale_genet.pdf\u0026Expires=1734172621\u0026Signature=OAv94DTVvcfRjq9aqWw0xMUfhZLIZ0PJ~9e2PQTlP8QBZMYyeXXuz6jBx5MnxChi2Omf94sgVQMcBE89sLBOrMFy8ckT2Qe3CHXBUTHiQVMazOBn~0HbKjvrZQcV1NRF8rqfADB865tE-WtgQeL8fXBO7-mpamsVjmiWBNXze~WwE3w1VzLQ6qAf4XI-jv6vn-ymPoXQlBzShAbQrabajT4k7vCHjPmqTmzfWX8egFmlCngwdRWL~0KC~ffwRtBDQBrTGy46924unWlI1AJz74YN2C3lrHWm1dkgwfdGfH6TiGpxa0WvLMtZGx67600vl9qFDNUNt3Lt1NXt2v2utw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_","translated_slug":"","page_count":9,"language":"en","content_type":"Work","summary":"Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright's fixation index, spatial autocorrelation statistics (Moran's I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran's I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":74760408,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/74760408/thumbnails/1.jpg","file_name":"6800187.pdf","download_url":"https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Temporal_aspects_of_the_fine_scale_genet.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/74760408/6800187-libre.pdf?1637128866=\u0026response-content-disposition=attachment%3B+filename%3DTemporal_aspects_of_the_fine_scale_genet.pdf\u0026Expires=1734172621\u0026Signature=OAv94DTVvcfRjq9aqWw0xMUfhZLIZ0PJ~9e2PQTlP8QBZMYyeXXuz6jBx5MnxChi2Omf94sgVQMcBE89sLBOrMFy8ckT2Qe3CHXBUTHiQVMazOBn~0HbKjvrZQcV1NRF8rqfADB865tE-WtgQeL8fXBO7-mpamsVjmiWBNXze~WwE3w1VzLQ6qAf4XI-jv6vn-ymPoXQlBzShAbQrabajT4k7vCHjPmqTmzfWX8egFmlCngwdRWL~0KC~ffwRtBDQBrTGy46924unWlI1AJz74YN2C3lrHWm1dkgwfdGfH6TiGpxa0WvLMtZGx67600vl9qFDNUNt3Lt1NXt2v2utw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics"},{"id":4480,"name":"Population Genetics","url":"https://www.academia.edu/Documents/in/Population_Genetics"},{"id":7666,"name":"Life history","url":"https://www.academia.edu/Documents/in/Life_history"},{"id":7972,"name":"Seed Dispersal","url":"https://www.academia.edu/Documents/in/Seed_Dispersal"},{"id":42324,"name":"Heredity","url":"https://www.academia.edu/Documents/in/Heredity"},{"id":43028,"name":"Genetic Diversity","url":"https://www.academia.edu/Documents/in/Genetic_Diversity"},{"id":52651,"name":"Spatial autocorrelation","url":"https://www.academia.edu/Documents/in/Spatial_autocorrelation"},{"id":55163,"name":"Enzymes","url":"https://www.academia.edu/Documents/in/Enzymes"},{"id":91566,"name":"Genetic Structure","url":"https://www.academia.edu/Documents/in/Genetic_Structure"},{"id":191815,"name":"Biological evolution","url":"https://www.academia.edu/Documents/in/Biological_evolution"},{"id":236377,"name":"Spatial Distribution","url":"https://www.academia.edu/Documents/in/Spatial_Distribution"},{"id":286413,"name":"Spatial Pattern","url":"https://www.academia.edu/Documents/in/Spatial_Pattern"},{"id":319956,"name":"Genetic Differentiation","url":"https://www.academia.edu/Documents/in/Genetic_Differentiation"},{"id":413195,"name":"Time Factors","url":"https://www.academia.edu/Documents/in/Time_Factors"},{"id":516151,"name":"Genetic Polymorphism","url":"https://www.academia.edu/Documents/in/Genetic_Polymorphism"},{"id":749302,"name":"Indexation","url":"https://www.academia.edu/Documents/in/Indexation"},{"id":1014085,"name":"Age Structure","url":"https://www.academia.edu/Documents/in/Age_Structure"},{"id":1571878,"name":"Cinnamomum","url":"https://www.academia.edu/Documents/in/Cinnamomum"}],"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="48374344"><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/48374344/Community_Structure_and_Undescribed_Species_Diversity_in_Non_Pollinating_Fig_Wasps_Associated_with_the_Strangler_Fig_Ficus_petiolaris"><img alt="Research paper thumbnail of Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris" class="work-thumbnail" src="https://attachments.academia-assets.com/67020011/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/48374344/Community_Structure_and_Undescribed_Species_Diversity_in_Non_Pollinating_Fig_Wasps_Associated_with_the_Strangler_Fig_Ficus_petiolaris">Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris</a></div><div class="wp-workCard_item"><span>Insect Systematics and Diversity</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecologic...</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">Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecological and evolutionary research due to their diversity, unusual reproductive biology, and highly coevolved interspecific relationships. Due to the ecological dependence of their interactions, fig wasps were once considered to be fig-species specific and to cospeciate with their hosts, however, a growing body of evidence reveals mixed support for species specificity and the importance of additional evolutionary processes (e.g., host switching) structuring these long-term interactions. Our research on the genus Idarnes Walker, 1843 (Hymenoptera, Agaonidae), a common non-pollinating wasp of New World fig flowers, reveals a community in which multiple wasp species coexist on the same host in space and time. Using both molecular and morphological data, we identify five distinct Idarnes lineages associated with a single host fig species, Ficus petiolaris Kunth, 1817 (Rosales, Moraceae). A compreh...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6689d432e02643fb0848419d822a8399" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:67020011,&quot;asset_id&quot;:48374344,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/67020011/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="48374344"><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="48374344"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48374344; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48374344]").text(description); $(".js-view-count[data-work-id=48374344]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 48374344; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='48374344']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 48374344, 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: "6689d432e02643fb0848419d822a8399" } } $('.js-work-strip[data-work-id=48374344]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48374344,"title":"Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris","translated_title":"","metadata":{"abstract":"Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecological and evolutionary research due to their diversity, unusual reproductive biology, and highly coevolved interspecific relationships. Due to the ecological dependence of their interactions, fig wasps were once considered to be fig-species specific and to cospeciate with their hosts, however, a growing body of evidence reveals mixed support for species specificity and the importance of additional evolutionary processes (e.g., host switching) structuring these long-term interactions. Our research on the genus Idarnes Walker, 1843 (Hymenoptera, Agaonidae), a common non-pollinating wasp of New World fig flowers, reveals a community in which multiple wasp species coexist on the same host in space and time. Using both molecular and morphological data, we identify five distinct Idarnes lineages associated with a single host fig species, Ficus petiolaris Kunth, 1817 (Rosales, Moraceae). A compreh...","publisher":"Oxford University Press (OUP)","publication_name":"Insect Systematics and Diversity"},"translated_abstract":"Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecological and evolutionary research due to their diversity, unusual reproductive biology, and highly coevolved interspecific relationships. Due to the ecological dependence of their interactions, fig wasps were once considered to be fig-species specific and to cospeciate with their hosts, however, a growing body of evidence reveals mixed support for species specificity and the importance of additional evolutionary processes (e.g., host switching) structuring these long-term interactions. Our research on the genus Idarnes Walker, 1843 (Hymenoptera, Agaonidae), a common non-pollinating wasp of New World fig flowers, reveals a community in which multiple wasp species coexist on the same host in space and time. Using both molecular and morphological data, we identify five distinct Idarnes lineages associated with a single host fig species, Ficus petiolaris Kunth, 1817 (Rosales, Moraceae). 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international journal of organic evolution</span><span>, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Evaluating trait correlations across species within a lineage via phylogenetic regression is fund...</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">Evaluating trait correlations across species within a lineage via phylogenetic regression is fundamental to comparative evolutionary biology, but when traits of interest are derived from two sets of lineages that coevolve with one another, methods for evaluating such patterns in a dual-phylogenetic context remain underdeveloped. Here, we extend multivariate permutation-based phylogenetic regression to evaluate trait correlations in two sets of interacting species while accounting for their respective phylogenies. This extension is appropriate for both univariate and multivariate response data, and may use one or more independent variables, including environmental covariates. Imperfect correspondence between species in the interacting lineages can also be accommodated, such as when species in one lineage associate with multiple species in the other, or when there are unmatched taxa in one or both lineages. For both univariate and multivariate data, the method displays appropriate typ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="940ce858302593d42084e488e3593411" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:67020390,&quot;asset_id&quot;:48374341,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/67020390/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="48374341"><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="48374341"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48374341; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48374341]").text(description); $(".js-view-count[data-work-id=48374341]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 48374341; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='48374341']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 48374341, 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: "940ce858302593d42084e488e3593411" } } $('.js-work-strip[data-work-id=48374341]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48374341,"title":"A phylogenetic comparative method for evaluating trait coevolution across two phylogenies for sets of interacting species","translated_title":"","metadata":{"abstract":"Evaluating trait correlations across species within a lineage via phylogenetic regression is fundamental to comparative evolutionary biology, but when traits of interest are derived from two sets of lineages that coevolve with one another, methods for evaluating such patterns in a dual-phylogenetic context remain underdeveloped. 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Here, we extend multivariate permutation-based phylogenetic regression to evaluate trait correlations in two sets of interacting species while accounting for their respective phylogenies. This extension is appropriate for both univariate and multivariate response data, and may use one or more independent variables, including environmental covariates. Imperfect correspondence between species in the interacting lineages can also be accommodated, such as when species in one lineage associate with multiple species in the other, or when there are unmatched taxa in one or both lineages. 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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="100055950"><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/100055950/Data_from_Comparison_of_quantitative_and_molecular_genetic_variation_of_native_vs_invasive_populations_of_purple_loosestrife_Lythrum_salicaria_L_Lythraceae_"><img alt="Research paper thumbnail of Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)" 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/100055950/Data_from_Comparison_of_quantitative_and_molecular_genetic_variation_of_native_vs_invasive_populations_of_purple_loosestrife_Lythrum_salicaria_L_Lythraceae_">Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Study of adaptive evolutionary changes in populations of invasive species can be advanced through...</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">Study of adaptive evolutionary changes in populations of invasive species can be advanced through the joint application of quantitative and population genetic methods. Using purple loosestrife as a model system, we investigated the relative roles of natural selection, genetic drift, ...</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="100055950"><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="100055950"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 100055950; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=100055950]").text(description); $(".js-view-count[data-work-id=100055950]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 100055950; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='100055950']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 100055950, 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" } } $('.js-work-strip[data-work-id=100055950]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":100055950,"title":"Data from: Comparison of quantitative and molecular genetic variation of native vs. invasive populations of purple loosestrife (Lythrum salicaria L., Lythraceae)","translated_title":"","metadata":{"abstract":"Study of adaptive evolutionary changes in populations of invasive species can be advanced through the joint application of quantitative and population genetic methods. 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Using purple loosestrife as a model system, we investigated the relative roles of natural selection, genetic drift, ...","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[],"research_interests":[],"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="92805533"><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/92805533/Population_Structure_and_Genetic_Diversity_of_the_Boll_Weevil_Coleoptera_Curculionidae_on_Gossypium_in_North_America"><img alt="Research paper thumbnail of Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America" class="work-thumbnail" src="https://attachments.academia-assets.com/95717002/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/92805533/Population_Structure_and_Genetic_Diversity_of_the_Boll_Weevil_Coleoptera_Curculionidae_on_Gossypium_in_North_America">Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a de...</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">Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity in Mexico on wild and cultivated cotton hosts (genus Gossypium) is poorly understood. Past studies using morphology, host use, and distribution records suggest that A.grandis grandis comprises three forms with host-associated characteristics: the southeastern form (from domesticated Gossypium hirsutum L., southeastern United States and northeastern Mexico), the thurberia form (from Gossypium thurberi Todaro, Arizona and northwestern Mexico), and the Mexican form (from multiple Gossypium species and other malvaceous plant genera in the remainder of Mexico and Central America). However, the phylogenetic relationships, host preferences, and distributions of these forms are not completely understood. An alternative hypothesis of an eastern and western form of the boll weevil is suggested by the sus...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="db100d12b59c49215670089229230ebe" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:95717002,&quot;asset_id&quot;:92805533,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/95717002/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="92805533"><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="92805533"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 92805533; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=92805533]").text(description); $(".js-view-count[data-work-id=92805533]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 92805533; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='92805533']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 92805533, 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: "db100d12b59c49215670089229230ebe" } } $('.js-work-strip[data-work-id=92805533]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":92805533,"title":"Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America","translated_title":"","metadata":{"abstract":"Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity in Mexico on wild and cultivated cotton hosts (genus Gossypium) is poorly understood. Past studies using morphology, host use, and distribution records suggest that A.grandis grandis comprises three forms with host-associated characteristics: the southeastern form (from domesticated Gossypium hirsutum L., southeastern United States and northeastern Mexico), the thurberia form (from Gossypium thurberi Todaro, Arizona and northwestern Mexico), and the Mexican form (from multiple Gossypium species and other malvaceous plant genera in the remainder of Mexico and Central America). However, the phylogenetic relationships, host preferences, and distributions of these forms are not completely understood. 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In this paper, we consider three typical sources of scoring errors capable of biasing biological conclusions: stuttering, large-allele dropout and null alleles. We describe methods to detect errors and propose conventions to mitigate scoring errors and report error rates in studies of wild populations. Finally, we discuss potential bias in ecological or evolutionary conclusions based on data sets containing these scoring errors.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="ddc4871ce49e99460ac0d65132783766" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:86564549,&quot;asset_id&quot;:80055739,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/86564549/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="80055739"><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="80055739"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 80055739; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=80055739]").text(description); $(".js-view-count[data-work-id=80055739]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 80055739; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='80055739']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 80055739, 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: "ddc4871ce49e99460ac0d65132783766" } } $('.js-work-strip[data-work-id=80055739]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":80055739,"title":"Mitigating scoring errors in microsatellite data from wild populations","translated_title":"","metadata":{"publisher":"Wiley-Blackwell","ai_title_tag":"Reducing Scoring Errors in Microsatellite Data of Wild Populations","grobid_abstract":"Microsatellite data are widely used to test ecological and evolutionary hypotheses in wild populations. 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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="73755085"><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/73755085/Extraordinarily_Precise_Nematode_Sex_Ratios_Adaptive_Responses_to_Vanishingly_Rare_Mating_Options"><img alt="Research paper thumbnail of Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options" class="work-thumbnail" src="https://attachments.academia-assets.com/82152140/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/73755085/Extraordinarily_Precise_Nematode_Sex_Ratios_Adaptive_Responses_to_Vanishingly_Rare_Mating_Options">Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options</a></div><div class="wp-workCard_item"><span>bioRxiv</span><span>, 2021</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Sex ratio theory predicts both mean sex ratio and variance under a range of population structures...</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">Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). In further contrast with their hosts, variances in nematode sex ratios are also consistently precise (significantly less than binomia...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6916d7460973c889504a050011497f84" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152140,&quot;asset_id&quot;:73755085,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152140/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755085"><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="73755085"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755085; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755085]").text(description); $(".js-view-count[data-work-id=73755085]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755085; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755085']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755085, 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: "6916d7460973c889504a050011497f84" } } $('.js-work-strip[data-work-id=73755085]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755085,"title":"Extraordinarily Precise Nematode Sex Ratios: Adaptive Responses to Vanishingly Rare Mating Options","translated_title":"","metadata":{"abstract":"Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). In further contrast with their hosts, variances in nematode sex ratios are also consistently precise (significantly less than binomia...","publication_date":{"day":null,"month":null,"year":2021,"errors":{}},"publication_name":"bioRxiv"},"translated_abstract":"Sex ratio theory predicts both mean sex ratio and variance under a range of population structures. Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. 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Here, we compare two genera of phoretic nematodes (Parasitodiplogaster and Ficophagus spp.) associated with twelve fig-pollinating wasp species in Panama. The host wasps exhibit classic Local Mate Competition: only inseminated females disperse from natal figs, and their offspring form mating pools that consist of scores of the adult offspring contributed by one or a few foundress mothers. In contrast, in both nematode genera, only sexually undifferentiated juveniles disperse, and their mating pools routinely consist of eight or fewer adults. Across all mating pool sizes, the sex ratios observed in both nematode genera are consistently female-biased (~0.34 males), which is markedly less female-biased than is often observed in the host wasps (~0.10 males). 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These community-level associations have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because identifying species interacting with focal mutualists and assessing their associated fitness benefits and costs is difficult, especially over space and through time. Here, we focus on a community comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) commensals/antagonists, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field experiments, we identified that all NPFWs are targets for infection by this nematode. Further, this infection can impact NPFWs more severely than either mutualistic partner, sugg...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="712805df8756d3e56fba0c6b9810f3ff" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152139,&quot;asset_id&quot;:73755084,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152139/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755084"><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="73755084"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755084; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755084]").text(description); $(".js-view-count[data-work-id=73755084]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755084; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755084']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755084, 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: "712805df8756d3e56fba0c6b9810f3ff" } } $('.js-work-strip[data-work-id=73755084]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755084,"title":"The enemy of my enemy is my friend: Nematode infection of pollinating and non-pollinating fig wasps has net benefits for the fig-fig wasp pollination mutualism","translated_title":"","metadata":{"abstract":"Mutualistic associations between species pairs are ubiquitous in nature but are also components of broader organismal community networks. These community-level associations have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because identifying species interacting with focal mutualists and assessing their associated fitness benefits and costs is difficult, especially over space and through time. Here, we focus on a community comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) commensals/antagonists, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field experiments, we identified that all NPFWs are targets for infection by this nematode. 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Although examples of mutualism are ubiquitous in nature, the ecology, evolution, and stability of mutualism has rarely been studied in the broader, multispecies community context in which they occur. The pollination mutualism between figs and fig wasps provides an excellent model system for investigating interactions between obligate mutualists and antagonists. Compared to the community of non-pollinating fig wasps that develop within figs inflorescences at the expense of fig seeds and pollinators, consequences of interactions between female pollinating wasps and their host-specialist nematode parasites is much less well understood. Here we focus on a tri-partite system comprised of a fig (Ficus petiolaris), pollinating wasp (Pegoscapus sp.), and nematode (Parasitodiplogaster sp.), investigating geographical variation in the incidence of attack and mechanisms through which nematodes may limit the fitness of their wasp hosts at successive life history stages. Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. The result that nematode infection appears to be largely benign-and the unexpected finding that nematodes frequently infect non-pollinating wasps-highlight gaps in our knowledge of pollinator-Parasitodiplogaster interactions and suggest previously unappreciated ways in which this nematode may influence fig and pollinator fitness, mutualism persistence, and non-pollinator community dynamics.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b8125c0f121feaaa2354da9e3f2fdc1f" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82152141,&quot;asset_id&quot;:73755082,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82152141/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&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="73755082"><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="73755082"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73755082; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73755082]").text(description); $(".js-view-count[data-work-id=73755082]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73755082; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73755082']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73755082, 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: "b8125c0f121feaaa2354da9e3f2fdc1f" } } $('.js-work-strip[data-work-id=73755082]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73755082,"title":"Figs, pollinators, and parasites: A longitudinal study of the effects of nematode infection on fig wasp fitness","translated_title":"","metadata":{"publisher":"Elsevier BV","ai_title_tag":"Impact of Nematode Infection on Fig Wasp Fitness","grobid_abstract":"Mutualisms are interactions between two species in which the fitnesses of both symbionts benefit from the relationship. 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Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. 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Observational data reveals that nematodes are ubiquitous across their host range in Baja California, Mexico; that the incidence of nematode infection varies across seasons within-and between locations, and that infected pollinators are sometimes associated with fitness declines through reduced offspring production. We find that moderate levels of infection (1-9 juvenile nematodes per host) are well tolerated by pollinator wasps whereas higher infection levels (≥10 nematodes per host) are correlated with a significant reduction in wasp lifespan and dispersal success. This overexploitation, however, is estimated to occur in only 2.8% of wasps in each generation. The result that nematode infection appears to be largely benign-and the unexpected finding that nematodes frequently infect non-pollinating wasps-highlight gaps in our knowledge of pollinator-Parasitodiplogaster interactions and suggest previously unappreciated ways in which this nematode may influence fig and pollinator fitness, mutualism persistence, and non-pollinator community dynamics.","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":82152141,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/82152141/thumbnails/1.jpg","file_name":"viewcontent.pdf","download_url":"https://www.academia.edu/attachments/82152141/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMCw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Figs_pollinators_and_parasites_A_longitu.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/82152141/viewcontent-libre.pdf?1647279829=\u0026response-content-disposition=attachment%3B+filename%3DFigs_pollinators_and_parasites_A_longitu.pdf\u0026Expires=1734172620\u0026Signature=aodA4EnZaBVp79GQNf431-x3MWFqZdtkp8LrP2TNbSAQtgB~fI0XaifMwkUB-zkeypjfTllxtwdMdHRaZYbNLSNxR7x-spusip2q5mZE~tesB5MP1V72EnjxNDX606BPgFxwlp9eop8422VJeyYY2wTv1djRy0qAAG9D2JnB-fjui8hDRK3dlcFbyHwmAwq8pmmaKzYmhYaX~jhbPo651ZYWGl0URN-4y0LnaFSp6GjEWcnb-lfJcczHqbNGROlVsRWIh3Fw0Yp1DE1p15Z2G5Ze84pSXNw2Q7tKtEoLCJlLc7J4SChoQb9VN8yLXOulEdPw0Ecw44UBI~RYPH7xJw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology"}],"urls":[{"id":18505715,"url":"https://api.elsevier.com/content/article/PII:S1146609X17300504?httpAccept=text/xml"}]}, 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="73755081"><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/73755081/Adam_P_Kuester_Robert_W_Jones_Thomas_W_Sappington_Kyung_Seok_Kim_Norman_B"><img alt="Research paper thumbnail of Adam P. Kuester, Robert W. Jones, Thomas W. Sappington, Kyung Seok Kim, Norman B" 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/73755081/Adam_P_Kuester_Robert_W_Jones_Thomas_W_Sappington_Kyung_Seok_Kim_Norman_B">Adam P. Kuester, Robert W. Jones, Thomas W. 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Accessions During Caged Germplasm Regeneration" class="work-thumbnail" src="https://attachments.academia-assets.com/82151947/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/73754957/Measuring_the_Effectiveness_of_Isolation_of_Brassica_napus_L_Accessions_During_Caged_Germplasm_Regeneration">Measuring the Effectiveness of Isolation of Brassica napus L. Accessions During Caged Germplasm Regeneration</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Gene flow, which is the successful movement of genes among populations by mating or migration 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">Gene flow, which is the successful movement of genes among populations by mating or migration of seeds or other propagules, has gained much interest in agriculture in recent years because of the widescale adoption of transgenic crops and concerns over transgene escape into the wild ( James 2004; Messeguer 2003; Stewart et al. 2003). Brassica napus (rapeseed), together with maize and sugar beet, have been identified among the species for which cross-pollination and transgene escape are concerns (Treu and Emberlin 2000). Disciplines Ecology and Evolutionary Biology | Genetics Comments This article is from PGR Newsletter issue no. 154 (2008): 14. Rights Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted. This article is available at Iowa State University Digital Repository: <a href="https://lib.dr.iastate.edu/eeob_ag_pubs/77" rel="nofollow">https://lib.dr.iastate.edu/eeob_ag_pubs/77</a> 1G&amp;#39;1~15 Pin Genetic Resources Na Article Latest (Fr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c238c05aa160d3a30e81a14beb0d50bc" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82151947,&quot;asset_id&quot;:73754957,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82151947/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="73754957"><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="73754957"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73754957; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73754957]").text(description); $(".js-view-count[data-work-id=73754957]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73754957; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73754957']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73754957, 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: "c238c05aa160d3a30e81a14beb0d50bc" } } $('.js-work-strip[data-work-id=73754957]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73754957,"title":"Measuring the Effectiveness of Isolation of Brassica napus L. 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This article is available at Iowa State University Digital Repository: https://lib.dr.iastate.edu/eeob_ag_pubs/77 1G\u0026#39;1~15 Pin Genetic Resources Na Article Latest (Fr...","publication_date":{"day":null,"month":null,"year":2008,"errors":{}}},"translated_abstract":"Gene flow, which is the successful movement of genes among populations by mating or migration of seeds or other propagules, has gained much interest in agriculture in recent years because of the widescale adoption of transgenic crops and concerns over transgene escape into the wild ( James 2004; Messeguer 2003; Stewart et al. 2003). Brassica napus (rapeseed), together with maize and sugar beet, have been identified among the species for which cross-pollination and transgene escape are concerns (Treu and Emberlin 2000). Disciplines Ecology and Evolutionary Biology | Genetics Comments This article is from PGR Newsletter issue no. 154 (2008): 14. Rights Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted. 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Brassica napus (rapeseed), together with maize and sugar beet, have been identified among the species for which cross-pollination and transgene escape are concerns (Treu and Emberlin 2000). Disciplines Ecology and Evolutionary Biology | Genetics Comments This article is from PGR Newsletter issue no. 154 (2008): 14. Rights Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted. This article is available at Iowa State University Digital Repository: https://lib.dr.iastate.edu/eeob_ag_pubs/77 1G\u0026#39;1~15 Pin Genetic Resources Na Article Latest (Fr...","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":82151947,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/82151947/thumbnails/1.jpg","file_name":"viewcontent.pdf","download_url":"https://www.academia.edu/attachments/82151947/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Measuring_the_Effectiveness_of_Isolation.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/82151947/viewcontent-libre.pdf?1647275731=\u0026response-content-disposition=attachment%3B+filename%3DMeasuring_the_Effectiveness_of_Isolation.pdf\u0026Expires=1734172621\u0026Signature=Jr~d9cM6jv8MWJUXWQlm8IfZdZgNkmv5rsr6mHF7YPKTBp7tBK2QYwSGis79rdFd0vzkVPFGgbRXeA7eEXfO3fhym4FOxDZUqxN6m4aZE-Xp7J-yfrCQHgtdY8ZRShX55XVi0DDLmVByrvADziNoCPyKhLCAeAoVeJ-SYapmcH972AvPlVDyuB0oGS~MHV1o7UJR76kLlRlucglxHORsqMYp0VNiSyfF6ogv~zlN1xzMe~aRf3045KW1rtlPhR88jfgc-kShUI5VKKRmOLupSgWw8feR0RW7OTonYxJ5rot~o1tsQhD7AqaxEa2BEHPX~H8c3gXYxchARhaBa3MZBQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":1601798,"name":"Plant genetic","url":"https://www.academia.edu/Documents/in/Plant_genetic"}],"urls":[{"id":18505659,"url":"https://lib.dr.iastate.edu/cgi/viewcontent.cgi?article=1077\u0026context=eeob_ag_pubs"}]}, 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="73754879"><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/73754879/Differential_effects_of_nematode_infection_on_pollinating_and_non_pollinating_fig_wasps_can_shared_antagonism_provide_net_benefits_to_a_mutualism"><img alt="Research paper thumbnail of Differential effects of nematode infection on pollinating and non-pollinating fig wasps: can shared antagonism provide net benefits to a mutualism?" class="work-thumbnail" src="https://attachments.academia-assets.com/82151854/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/73754879/Differential_effects_of_nematode_infection_on_pollinating_and_non_pollinating_fig_wasps_can_shared_antagonism_provide_net_benefits_to_a_mutualism">Differential effects of nematode infection on pollinating and non-pollinating fig wasps: can shared antagonism provide net benefits to a mutualism?</a></div><div class="wp-workCard_item"><span>The Journal of animal ecology</span><span>, 2021</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Species pairs that form mutualistic associations are also components of broader organismal commun...</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">Species pairs that form mutualistic associations are also components of broader organismal community networks. These interaction networks have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because characterizing the impacts of species interacting with focal mutualists is often difficult. How is the fitness of mutualists impacted by the co-occurring interactive network of community associates? We investigate this context using a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field observations we characterize the ecological roles of these mutualist-associated organisms to identify key antagonists. We then investigated how pote...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5ef971d6e6086429a4541a96c2c204db" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:82151854,&quot;asset_id&quot;:73754879,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/82151854/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="73754879"><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="73754879"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 73754879; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=73754879]").text(description); $(".js-view-count[data-work-id=73754879]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 73754879; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='73754879']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 73754879, 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: "5ef971d6e6086429a4541a96c2c204db" } } $('.js-work-strip[data-work-id=73754879]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":73754879,"title":"Differential effects of nematode infection on pollinating and non-pollinating fig wasps: can shared antagonism provide net benefits to a mutualism?","translated_title":"","metadata":{"abstract":"Species pairs that form mutualistic associations are also components of broader organismal community networks. These interaction networks have shaped the evolution of individual mutualisms through interspecific interactions ranging from secondarily mutualistic to intensely antagonistic. Our understanding of this complex context remains limited because characterizing the impacts of species interacting with focal mutualists is often difficult. How is the fitness of mutualists impacted by the co-occurring interactive network of community associates? We investigate this context using a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals, and a nematode previously believed to be associated only with the pollinator wasp mutualist. Through repeated sampling and field observations we characterize the ecological roles of these mutualist-associated organisms to identify key antagonists. 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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="69436104"><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/69436104/Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps"><img alt="Research paper thumbnail of Plant connectivity underlies plant-pollinator-exploiter distributions inFicus petiolarisand associated pollinating and non-pollinating fig wasps" class="work-thumbnail" src="https://attachments.academia-assets.com/79535585/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/69436104/Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps">Plant connectivity underlies plant-pollinator-exploiter distributions inFicus petiolarisand associated pollinating and non-pollinating fig wasps</a></div><div class="wp-workCard_item"><span>Oikos</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="4234b10f1858d2fe90d4f104b1fceb8a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:79535585,&quot;asset_id&quot;:69436104,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/79535585/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="69436104"><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="69436104"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 69436104; 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In nursery pollination mutualisms, pollinators reproduce within the inflorescence they pollinate, with benefits and costs being measured in the numbers of pollinator offspring and seeds produced. This type of mutualism is also typically exploited by seed-consuming nonpollinators that obtain resources from plants without providing pollination services. Theory predicts that the rate at which pollen-bearing \"foundresses\" visit a plant will strongly affect the plant's production of pollinator offspring, non-pollinator offspring, and seeds. Spatially aggregated plants are predicted to have high rates of foundress visitation, increasing pollinator and seed production, and decreasing non-pollinator production; very high foundress visitation may also decrease seed production indirectly through the production of pollinators. Working with a nursery mutualism comprised of interactions to benefits and costs: 1) foundress density increases with host-tree connectivity, 2) pollinator production increases with foundress density, and 3) nonpollinator production and 4) seed production decrease with pollinator production. We also directly test how tree connectivity affects non-pollinator production. We find strong support for our four hypotheses, and we conclude that tree connectivity is a key driver of foundress visitation, thereby strongly affecting spatial distributions in the F. petiolaris community. We also find that foundress visitation decreases at the northernmost edge of the F. petiolaris range. Finally, we find species-specific effects of tree connectivity on non-pollinators to be strongly correlated with previously estimated non-pollinator dispersal abilities. We conclude that plant connectivity is highly important for predicting plant-pollinator-exploiter dynamics, and discuss the implications of our results for species coexistence and adaptation.","publication_name":"Oikos"},"translated_abstract":null,"internal_url":"https://www.academia.edu/69436104/Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps","translated_internal_url":"","created_at":"2022-01-25T10:08:34.007-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":41682648,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":79535585,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/79535585/thumbnails/1.jpg","file_name":"Duthie_et_al_2016_Oikos.pdf","download_url":"https://www.academia.edu/attachments/79535585/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Plant_connectivity_underlies_plant_polli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/79535585/Duthie_et_al_2016_Oikos-libre.pdf?1643137931=\u0026response-content-disposition=attachment%3B+filename%3DPlant_connectivity_underlies_plant_polli.pdf\u0026Expires=1734172621\u0026Signature=eCfkZJs3GZcK9Rmp1au2NxZq0Zy~KFykSjMn3Q93W3XgdPhKlUNwjuAk3u8elrf3a26GjWCGNPjonjQqjrZbg3C~~Q3S9eI0G4ynIGJ6Nra4ZI6bu3V4bMUSEFI0ZztxmJt9bZ9Kkz-wcEjgwmSQ-D0kgjVIU~NTa7B0lHNFWQMheUO5FHsiovm~pB9Hrw7lSQpdOc3XG3pUNDeDZWXwlCU2LVq2rNpEkt5Epcq7bH-xa2KnK1HM5MG4l5Sp2-ltwKcgMAcVziM6jafadY3cvWzj2JNUAcaGh5M2QVvyu0zF7N8HgzGeJ4aVBx~wXVdkgp9E1PVDC7zooegvgh1XPA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Plant_connectivity_underlies_plant_pollinator_exploiter_distributions_inFicus_petiolarisand_associated_pollinating_and_non_pollinating_fig_wasps","translated_slug":"","page_count":32,"language":"en","content_type":"Work","summary":null,"owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":79535585,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/79535585/thumbnails/1.jpg","file_name":"Duthie_et_al_2016_Oikos.pdf","download_url":"https://www.academia.edu/attachments/79535585/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Plant_connectivity_underlies_plant_polli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/79535585/Duthie_et_al_2016_Oikos-libre.pdf?1643137931=\u0026response-content-disposition=attachment%3B+filename%3DPlant_connectivity_underlies_plant_polli.pdf\u0026Expires=1734172621\u0026Signature=eCfkZJs3GZcK9Rmp1au2NxZq0Zy~KFykSjMn3Q93W3XgdPhKlUNwjuAk3u8elrf3a26GjWCGNPjonjQqjrZbg3C~~Q3S9eI0G4ynIGJ6Nra4ZI6bu3V4bMUSEFI0ZztxmJt9bZ9Kkz-wcEjgwmSQ-D0kgjVIU~NTa7B0lHNFWQMheUO5FHsiovm~pB9Hrw7lSQpdOc3XG3pUNDeDZWXwlCU2LVq2rNpEkt5Epcq7bH-xa2KnK1HM5MG4l5Sp2-ltwKcgMAcVziM6jafadY3cvWzj2JNUAcaGh5M2QVvyu0zF7N8HgzGeJ4aVBx~wXVdkgp9E1PVDC7zooegvgh1XPA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology"},{"id":156991,"name":"Oikos","url":"https://www.academia.edu/Documents/in/Oikos"}],"urls":[{"id":16890365,"url":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Foik.02905"}]}, 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="61821584"><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/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_"><img alt="Research paper thumbnail of Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)" class="work-thumbnail" src="https://attachments.academia-assets.com/74760408/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/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_">Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)</a></div><div class="wp-workCard_item"><span>Heredity</span><span>, 2003</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tr...</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">Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright&#39;s fixation index, spatial autocorrelation statistics (Moran&#39;s I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran&#39;s I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="82048dc14d4c9d3034c0d1b425cbf6db" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:74760408,&quot;asset_id&quot;:61821584,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&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="61821584"><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="61821584"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 61821584; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=61821584]").text(description); $(".js-view-count[data-work-id=61821584]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 61821584; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='61821584']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 61821584, 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: "82048dc14d4c9d3034c0d1b425cbf6db" } } $('.js-work-strip[data-work-id=61821584]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":61821584,"title":"Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)","translated_title":"","metadata":{"publisher":"Springer Nature","ai_title_tag":"Genetic Structure of Cinnamomum insularimontanum Across Age Classes","grobid_abstract":"Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright's fixation index, spatial autocorrelation statistics (Moran's I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran's I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.","publication_date":{"day":null,"month":null,"year":2003,"errors":{}},"publication_name":"Heredity","grobid_abstract_attachment_id":74760408},"translated_abstract":null,"internal_url":"https://www.academia.edu/61821584/Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_","translated_internal_url":"","created_at":"2021-11-16T21:19:54.315-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":41682648,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":74760408,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/74760408/thumbnails/1.jpg","file_name":"6800187.pdf","download_url":"https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Temporal_aspects_of_the_fine_scale_genet.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/74760408/6800187-libre.pdf?1637128866=\u0026response-content-disposition=attachment%3B+filename%3DTemporal_aspects_of_the_fine_scale_genet.pdf\u0026Expires=1734172621\u0026Signature=OAv94DTVvcfRjq9aqWw0xMUfhZLIZ0PJ~9e2PQTlP8QBZMYyeXXuz6jBx5MnxChi2Omf94sgVQMcBE89sLBOrMFy8ckT2Qe3CHXBUTHiQVMazOBn~0HbKjvrZQcV1NRF8rqfADB865tE-WtgQeL8fXBO7-mpamsVjmiWBNXze~WwE3w1VzLQ6qAf4XI-jv6vn-ymPoXQlBzShAbQrabajT4k7vCHjPmqTmzfWX8egFmlCngwdRWL~0KC~ffwRtBDQBrTGy46924unWlI1AJz74YN2C3lrHWm1dkgwfdGfH6TiGpxa0WvLMtZGx67600vl9qFDNUNt3Lt1NXt2v2utw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Temporal_aspects_of_the_fine_scale_genetic_structure_in_a_population_of_Cinnamomum_insularimontanum_Lauraceae_","translated_slug":"","page_count":9,"language":"en","content_type":"Work","summary":"Cinnamomum insularimontanum Hayata (Lauraceae) is an insect-pollinated, broad-leaved evergreen tree with birddispersed seeds. We used allozyme loci, Wright's fixation index, spatial autocorrelation statistics (Moran's I), and coancestry measures to examine changes in genetic structure among four age-classes within a recently founded study population (60 Â 100 m area) in southern Korea. There were no significant differences in expected heterozygosity among age classes. However, significant genetic differentiation among age classes was detected (Po0.0001). Fixation indices within age classes showed significant deficits of observed heterozygosity, which may be caused by partial selfing. The homogeneity of genetic structure among four age-classes may reflect similar spatial patterns of seed immigration from surrounding populations occurring year after year. Finally, the average Moran's I and coancestry estimates indicated essentially random spatial distributions of alleles for each of the four age-classes and between seedlings and 2-4 year juveniles vs adult trees. These findings are very similar to those observed in the same study area for another member of the Lauraceae, Neolitsea sericea, which has a very similar life history and ecological characteristics (ie, bird-dispersed fruits, insect pollination, and a similar age structure). Together, these results suggest that the fleshy drupes of lauraceous species represent an adaptation to aid in the independent dispersal of seed by birds, which in turn may increase the genetic diversity of founders colonizing new habitats.","owner":{"id":41682648,"first_name":"John","middle_initials":null,"last_name":"Nason","page_name":"NasonJohn","domain_name":"independent","created_at":"2016-01-18T09:51:28.345-08:00","display_name":"John Nason","url":"https://independent.academia.edu/NasonJohn"},"attachments":[{"id":74760408,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/74760408/thumbnails/1.jpg","file_name":"6800187.pdf","download_url":"https://www.academia.edu/attachments/74760408/download_file?st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&st=MTczNDE2OTAyMSw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Temporal_aspects_of_the_fine_scale_genet.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/74760408/6800187-libre.pdf?1637128866=\u0026response-content-disposition=attachment%3B+filename%3DTemporal_aspects_of_the_fine_scale_genet.pdf\u0026Expires=1734172621\u0026Signature=OAv94DTVvcfRjq9aqWw0xMUfhZLIZ0PJ~9e2PQTlP8QBZMYyeXXuz6jBx5MnxChi2Omf94sgVQMcBE89sLBOrMFy8ckT2Qe3CHXBUTHiQVMazOBn~0HbKjvrZQcV1NRF8rqfADB865tE-WtgQeL8fXBO7-mpamsVjmiWBNXze~WwE3w1VzLQ6qAf4XI-jv6vn-ymPoXQlBzShAbQrabajT4k7vCHjPmqTmzfWX8egFmlCngwdRWL~0KC~ffwRtBDQBrTGy46924unWlI1AJz74YN2C3lrHWm1dkgwfdGfH6TiGpxa0WvLMtZGx67600vl9qFDNUNt3Lt1NXt2v2utw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics"},{"id":4480,"name":"Population Genetics","url":"https://www.academia.edu/Documents/in/Population_Genetics"},{"id":7666,"name":"Life history","url":"https://www.academia.edu/Documents/in/Life_history"},{"id":7972,"name":"Seed Dispersal","url":"https://www.academia.edu/Documents/in/Seed_Dispersal"},{"id":42324,"name":"Heredity","url":"https://www.academia.edu/Documents/in/Heredity"},{"id":43028,"name":"Genetic Diversity","url":"https://www.academia.edu/Documents/in/Genetic_Diversity"},{"id":52651,"name":"Spatial autocorrelation","url":"https://www.academia.edu/Documents/in/Spatial_autocorrelation"},{"id":55163,"name":"Enzymes","url":"https://www.academia.edu/Documents/in/Enzymes"},{"id":91566,"name":"Genetic Structure","url":"https://www.academia.edu/Documents/in/Genetic_Structure"},{"id":191815,"name":"Biological evolution","url":"https://www.academia.edu/Documents/in/Biological_evolution"},{"id":236377,"name":"Spatial Distribution","url":"https://www.academia.edu/Documents/in/Spatial_Distribution"},{"id":286413,"name":"Spatial Pattern","url":"https://www.academia.edu/Documents/in/Spatial_Pattern"},{"id":319956,"name":"Genetic Differentiation","url":"https://www.academia.edu/Documents/in/Genetic_Differentiation"},{"id":413195,"name":"Time Factors","url":"https://www.academia.edu/Documents/in/Time_Factors"},{"id":516151,"name":"Genetic Polymorphism","url":"https://www.academia.edu/Documents/in/Genetic_Polymorphism"},{"id":749302,"name":"Indexation","url":"https://www.academia.edu/Documents/in/Indexation"},{"id":1014085,"name":"Age Structure","url":"https://www.academia.edu/Documents/in/Age_Structure"},{"id":1571878,"name":"Cinnamomum","url":"https://www.academia.edu/Documents/in/Cinnamomum"}],"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="48374344"><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/48374344/Community_Structure_and_Undescribed_Species_Diversity_in_Non_Pollinating_Fig_Wasps_Associated_with_the_Strangler_Fig_Ficus_petiolaris"><img alt="Research paper thumbnail of Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris" class="work-thumbnail" src="https://attachments.academia-assets.com/67020011/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/48374344/Community_Structure_and_Undescribed_Species_Diversity_in_Non_Pollinating_Fig_Wasps_Associated_with_the_Strangler_Fig_Ficus_petiolaris">Community Structure and Undescribed Species Diversity in Non-Pollinating Fig Wasps Associated with the Strangler Fig Ficus petiolaris</a></div><div class="wp-workCard_item"><span>Insect Systematics and Diversity</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecologic...</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">Figs and their associated mutualistic and parasitic wasps have been a focus of intensive ecological and evolutionary research due to their diversity, unusual reproductive biology, and highly coevolved interspecific relationships. Due to the ecological dependence of their interactions, fig wasps were once considered to be fig-species specific and to cospeciate with their hosts, however, a growing body of evidence reveals mixed support for species specificity and the importance of additional evolutionary processes (e.g., host switching) structuring these long-term interactions. Our research on the genus Idarnes Walker, 1843 (Hymenoptera, Agaonidae), a common non-pollinating wasp of New World fig flowers, reveals a community in which multiple wasp species coexist on the same host in space and time. Using both molecular and morphological data, we identify five distinct Idarnes lineages associated with a single host fig species, Ficus petiolaris Kunth, 1817 (Rosales, Moraceae). 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international journal of organic evolution</span><span>, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Evaluating trait correlations across species within a lineage via phylogenetic regression is fund...</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">Evaluating trait correlations across species within a lineage via phylogenetic regression is fundamental to comparative evolutionary biology, but when traits of interest are derived from two sets of lineages that coevolve with one another, methods for evaluating such patterns in a dual-phylogenetic context remain underdeveloped. Here, we extend multivariate permutation-based phylogenetic regression to evaluate trait correlations in two sets of interacting species while accounting for their respective phylogenies. This extension is appropriate for both univariate and multivariate response data, and may use one or more independent variables, including environmental covariates. Imperfect correspondence between species in the interacting lineages can also be accommodated, such as when species in one lineage associate with multiple species in the other, or when there are unmatched taxa in one or both lineages. 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