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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 Karina Silva-brandão</h3></div><div class="js-work-strip profile--work_container" data-work-id="116508592"><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/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_"><img alt="Research paper thumbnail of Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]" class="work-thumbnail" src="https://attachments.academia-assets.com/112619273/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/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_">Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]</a></div><div class="wp-workCard_item"><span>Scopus</span><span>, 2009</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="d378225a0ee584ccdbdaf0d41eada6b1" 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});</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: "d378225a0ee584ccdbdaf0d41eada6b1" } } $('.js-work-strip[data-work-id=116508592]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508592,"title":"Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]","translated_title":"","metadata":{"publisher":"Institute of Electrical and Electronics Engineers","grobid_abstract":"Barcoding Lepidoptera: Situação Atual e Perspectivas sobre a Utilidade de uma Técnica Controversa RESUMO-A necessidade crescente de identificação e delimitação de novas espécies, ou de espécies crípticas já estabelecidas, que estão sendo perdidas a uma taxa também crescente, tem levado diversos especialistas a utilizarem uma variedade de ferramentas moleculares e computacionais. Neste momento, taxonomistas devem estar atentos a toda nova tecnologia disponível na chamada \"revolução dirigida pela tecnologia\" na sistemática, que tem entre as novas ferramentas moleculares a utilização de \"DNA barcodes\". O uso de \"DNA barcode\" tem sido amplamente discutido por aqueles que aplicam essa abordagem com sucesso para identificar e diagnosticar espécies, e por aqueles que acreditam que são tantos os problemas no uso desse marcador molecular que não se justifica seu emprego. Para insetos da ordem Lepidoptera nenhum lado parece estar totalmente certo ou errado e, embora alguns grupos de lepidópteros tenham sido resolvidos taxonomicamente pelo uso exclusivo ou adicional desse marcador, para outros o \"barcode\" ajudou pouco a resolver problemas taxonômicos. Aqui nós apresentamos brevemente prós e contras do uso de \"DNA barcode\" como ferramenta em estudos taxonômicos, com atenção especial para estudos com grupos de Lepidoptera desenvolvidos nos últimos anos.","publication_date":{"day":null,"month":null,"year":2009,"errors":{}},"publication_name":"Scopus","grobid_abstract_attachment_id":112619273},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_","translated_internal_url":"","created_at":"2024-03-21T05:08:55.351-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619273,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619273/thumbnails/1.jpg","file_name":"s1519-566x200900040000120240321-1-tgntxx.pdf","download_url":"https://www.academia.edu/attachments/112619273/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Barcoding_Lepidoptera_Current_Situation.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619273/s1519-566x200900040000120240321-1-tgntxx-libre.pdf?1711023089=\u0026response-content-disposition=attachment%3B+filename%3DBarcoding_Lepidoptera_Current_Situation.pdf\u0026Expires=1732776032\u0026Signature=gXHkosW3bSfxlQQEs4s0TYctaJAZpMh1V0SkjjIqNMdnsN4PfCnUs-F7PIhHBWyL-YiUtJSfExtaztFVvrjGUwfX3lV9pxbvkcVwiWsZhDTIGpPkhYz5HpN-7h35hQ~eoboWJUz9pe7XBPLoIt0DPN1YjiIL-O-oQ4WgQNYnmM3~W9ZjH2xNaAfHdyraP81UXTBnlbxMdamRo~kYjSjQrjWl591ZJ-~gJiQ4hi0WV~IxIMQivrg7haN1QAJdpcGgsAREqv6KIEubAvdYpnT1oKk3QPMEZhUZ9crTR3ohfPu4f6FjzmMKfl5XXUNJsKmIPSqhB6Adb6G64mJNf0R87A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situação_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_Técnica_Controversa_","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619273,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619273/thumbnails/1.jpg","file_name":"s1519-566x200900040000120240321-1-tgntxx.pdf","download_url":"https://www.academia.edu/attachments/112619273/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Barcoding_Lepidoptera_Current_Situation.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619273/s1519-566x200900040000120240321-1-tgntxx-libre.pdf?1711023089=\u0026response-content-disposition=attachment%3B+filename%3DBarcoding_Lepidoptera_Current_Situation.pdf\u0026Expires=1732776032\u0026Signature=gXHkosW3bSfxlQQEs4s0TYctaJAZpMh1V0SkjjIqNMdnsN4PfCnUs-F7PIhHBWyL-YiUtJSfExtaztFVvrjGUwfX3lV9pxbvkcVwiWsZhDTIGpPkhYz5HpN-7h35hQ~eoboWJUz9pe7XBPLoIt0DPN1YjiIL-O-oQ4WgQNYnmM3~W9ZjH2xNaAfHdyraP81UXTBnlbxMdamRo~kYjSjQrjWl591ZJ-~gJiQ4hi0WV~IxIMQivrg7haN1QAJdpcGgsAREqv6KIEubAvdYpnT1oKk3QPMEZhUZ9crTR3ohfPu4f6FjzmMKfl5XXUNJsKmIPSqhB6Adb6G64mJNf0R87A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":422,"name":"Computer Science","url":"https://www.academia.edu/Documents/in/Computer_Science"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":27756,"name":"DNA Barcoding","url":"https://www.academia.edu/Documents/in/DNA_Barcoding"},{"id":31356,"name":"Lepidoptera","url":"https://www.academia.edu/Documents/in/Lepidoptera"},{"id":106145,"name":"Classification","url":"https://www.academia.edu/Documents/in/Classification"},{"id":247162,"name":"Scopus","url":"https://www.academia.edu/Documents/in/Scopus"}],"urls":[{"id":40491394,"url":"http://repositorio.unicamp.br/jspui/bitstream/REPOSIP/91891/1/2-s2.0-70349976028.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="116508590"><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/116508590/There_is_more_than_chitin_synthase_in_insect_resistance_to_benzoylureas_molecular_markers_associated_with_teflubenzuron_resistance_in_Spodoptera_frugiperda"><img alt="Research paper thumbnail of There is more than chitin synthase in insect resistance to benzoylureas: molecular markers associated with teflubenzuron resistance in Spodoptera frugiperda" class="work-thumbnail" src="https://attachments.academia-assets.com/112619237/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/116508590/There_is_more_than_chitin_synthase_in_insect_resistance_to_benzoylureas_molecular_markers_associated_with_teflubenzuron_resistance_in_Spodoptera_frugiperda">There is more than chitin synthase in insect resistance to benzoylureas: molecular markers associated with teflubenzuron resistance in Spodoptera frugiperda</a></div><div class="wp-workCard_item"><span>Journal of Pest Science</span><span>, Apr 17, 2021</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b516fd70dc5b7ac47da41f21b6e0bda1" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619237,"asset_id":116508590,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619237/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508590"><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="116508590"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508590; 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Reports on field-evolved resistance of lepidopteran pests to chitin synthesis inhibitors and the selection of laboratory resistant strains to these products require a detailed investigation on the resistance mechanisms and on the identification of molecular markers to support the implementation of efficient monitoring and resistance management programs. Teflubenzuron is a chitin synthesis inhibitor highly effective in controlling lepidopteran pests, including nowadays the world widely distributed fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith, 1797) (Lepidoptera: Noctuidae). We report the selection of a laboratory strain of S. frugiperda resistant to teflubenzuron, and its use for the characterization of the inheritance of resistance, evaluation of cross-resistance to other chitin-synthesis inhibitors and the identification of a set of single nucleotide polymorphisms (SNPs) for use as candidate molecular markers for monitoring the evolution of resistance of S. frugiperda to teflubenzuron. The resistance of the selected strain of S. frugiperda to teflubenzuron was characterized as polygenic, autosomal, and incompletely recessive. The resistance ratio observed was nearly 1,365-fold. Teflubenzuron-resistant strain showed some cross-resistance to lufenuron and novaluron but not to chlorfluazuron. We also detected a set of 72 SNPs that could support monitoring of the resistance frequency to teflubenzuron in field populations. Our data contribute to the understanding of the resistance mechanisms and the inheritance of polygenic resistance of S. frugiperda to benzoylureas. We also contribute with candidate markers as tools for monitoring the emergence and spread of teflubenzuron resistance in S. frugiperda.","publication_date":{"day":17,"month":4,"year":2021,"errors":{}},"publication_name":"Journal of Pest 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profile--work_container" data-work-id="116508589"><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/116508589/Morphological_and_molecular_marker_contributions_to_disentangling_the_cryptic_i_Hermeuptychia_hermes_i_species_complex_Nymphalidae_Satyrinae_Euptychiina_"><img alt="Research paper thumbnail of Morphological and molecular marker contributions to disentangling the cryptic<i>Hermeuptychia hermes</i>species complex (Nymphalidae: Satyrinae: Euptychiina)" class="work-thumbnail" src="https://attachments.academia-assets.com/112619301/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/116508589/Morphological_and_molecular_marker_contributions_to_disentangling_the_cryptic_i_Hermeuptychia_hermes_i_species_complex_Nymphalidae_Satyrinae_Euptychiina_">Morphological and molecular marker contributions to disentangling the cryptic<i>Hermeuptychia hermes</i>species complex (Nymphalidae: Satyrinae: Euptychiina)</a></div><div class="wp-workCard_item"><span>Molecular Ecology Resources</span><span>, Sep 6, 2013</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5cc353b8f0a28fe7f23bcdf78bcdf874" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619301,"asset_id":116508589,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619301/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&s=profile"><span><i class="fa 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widespread through the Americas, from Argentina to the southern United States of America. All eight recognized species within Hermeuptychia are small and brown, with very similar interspecific external morphologies and intraspecifically variable ocelli patterns that render taxonomic identification based on morphology difficult. In our study, we surveyed variability within Hermeuptychia, and evaluate species boundaries based on molecular data (sequences of the \"barcode\" mitochondrial DNA COI gene) and morphology (mainly male genitalia), using a phylogenetic approach. We found eight DNA-based and twelve morphological groups in our sampling. Species names were assigned based mainly on comparisons with male genitalia morphology descriptions corresponding to name-bearing type specimens. Morphological and DNA variability were highly congruent, with the exception of group H, the H. cucullina complex. Also, the barcode region showed a clear threshold for intra and interspecific mean distances around 2%. Based on these results we circumscribe the species boundaries in the genus Hermeuptychia, and discuss conflicts between mitochondrial genes and classic morphological approaches for identifying and delimiting species. Our study revealed cryptic diversity within a ubiquitous genus of Neotropical butterflies.","publication_date":{"day":6,"month":9,"year":2013,"errors":{}},"publication_name":"Molecular Ecology 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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="116508587"><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/116508587/Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos"><img alt="Research paper thumbnail of Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of <i>Spodoptera frugiperda</i> to lambda‐cyhalothrin and chlorpyrifos" 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/116508587/Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos">Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of <i>Spodoptera frugiperda</i> to lambda‐cyhalothrin and chlorpyrifos</a></div><div class="wp-workCard_item"><span>Pest Management Science</span><span>, Mar 1, 2023</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several reco...</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">BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.</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="116508587"><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="116508587"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508587; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=116508587]").text(description); $(".js-view-count[data-work-id=116508587]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 116508587; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='116508587']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 116508587, 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" } } $('.js-work-strip[data-work-id=116508587]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508587,"title":"Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of \u003ci\u003eSpodoptera frugiperda\u003c/i\u003e to lambda‐cyhalothrin and chlorpyrifos","translated_title":"","metadata":{"abstract":"BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.","publisher":"Wiley","publication_date":{"day":1,"month":3,"year":2023,"errors":{}},"publication_name":"Pest Management Science"},"translated_abstract":"BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical 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href="https://www.academia.edu/116508582/A_new_genus_and_species_of_Euptychiina_Lepidoptera_Nymphalidae_Satyrinae_from_southern_Brazil">A new genus and species of Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from southern Brazil</a></div><div class="wp-workCard_item"><span>Neotropical Entomology</span><span>, Apr 1, 2011</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="4f9abfad9bf08a3d429def63963ee5de" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619241,"asset_id":116508582,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619241/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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 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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="116508578"><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/116508578/Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos"><img alt="Research paper thumbnail of Susceptibility monitoring and the molecular characterization of resistance of Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin and chlorpyrifos" class="work-thumbnail" src="https://attachments.academia-assets.com/112619268/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/116508578/Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos">Susceptibility monitoring and the molecular characterization of resistance of Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin and chlorpyrifos</a></div><div class="wp-workCard_item"><span>bioRxiv (Cold Spring Harbor Laboratory)</span><span>, Nov 19, 2021</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="1a9bd4ff98576370162f985faceb634c" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619268,"asset_id":116508578,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619268/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508578"><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="116508578"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508578; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "1a9bd4ff98576370162f985faceb634c" } } $('.js-work-strip[data-work-id=116508578]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508578,"title":"Susceptibility monitoring and the molecular characterization of resistance of Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin and chlorpyrifos","translated_title":"","metadata":{"publisher":"Cold Spring Harbor Laboratory","grobid_abstract":"Spodoptera frugiperda (J. E. Smith) is a serious and widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda-cyhalothrin (pyrethroid). In this study, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda-cyhalothrin (197 populations) collected from major maize-growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of chlorpyrifos-and lambda-cyhalothrin-resistant strains to a susceptible reference strain (Sfss) of S. frugiperda. Laboratory-guided assays to monitor larval susceptibility detected average survival ranging from 29.3% to 36.0% to chlorpyrifos, and 23.1% to 68.0% to lambdacyhalothrin at diagnostic concentration, based on LC99 of the susceptible reference strain of each insecticide. The resistance ratio of the chlorpyrifos-resistant strain (Clo-rr) was 25.4-fold and of the lambda-cyhalothrin-resistant strain (Lam-rr) was 217-fold. Differential gene expression analyses between resistant vs susceptible strains identified 1,098 differentially expressed genes (DEGs) between Clo-rr and Sf-ss, and 303 DEGs between Lam-rr and Sf-ss. Functional analyses of the DEGs revealed the up-regulation of several detoxification enzymes, mainly cytochrome P450 belonging to the CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box O (FoxO) were also up-regulated. Our data points that the resistance mechanisms of Clo-rr and Lam-rr strains of S. frugiperda to chlorpyrifos and lambda-cyhalothrin are mainly mediated by enzyme detoxification.","publication_date":{"day":19,"month":11,"year":2021,"errors":{}},"publication_name":"bioRxiv (Cold Spring Harbor Laboratory)","grobid_abstract_attachment_id":112619268},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508578/Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos","translated_internal_url":"","created_at":"2024-03-21T05:08:54.010-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619268,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619268/thumbnails/1.jpg","file_name":"2021.11.17.469006.full.pdf","download_url":"https://www.academia.edu/attachments/112619268/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Susceptibility_monitoring_and_the_molecu.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619268/2021.11.17.469006.full-libre.pdf?1711023019=\u0026response-content-disposition=attachment%3B+filename%3DSusceptibility_monitoring_and_the_molecu.pdf\u0026Expires=1732776032\u0026Signature=I6EGpES6flLm8r8HXiyCWnC2aIJumG0dh~~IhqUgMNC~9J88l4HYaliwym61wLrIokgz-kxB3KAOE71Zw8sGmtTK-KvVGfz~18~C-SmmiarOYAwRYksA~JrKI2cTBuQC7HujEG3cnEcKvfP8t-J1jlkuu-bQ2hS94Kw9TlVevu8Kfqd9fbapPt7VnBRwyw39TY3ebt7nlR6GFZhND1dot0kwDwIbaY34OFd~c97HVz6370OMKnQwW6iRP4Na8plZB-ro9M7Ad0z34oBZAN9tkfx9NipI64Ez7whkBl0VfRGg1RQBw-sG1iJk1awyFbOjqGCZ89UaG~mZkds9dyaQ8w__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos","translated_slug":"","page_count":31,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619268,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619268/thumbnails/1.jpg","file_name":"2021.11.17.469006.full.pdf","download_url":"https://www.academia.edu/attachments/112619268/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Susceptibility_monitoring_and_the_molecu.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619268/2021.11.17.469006.full-libre.pdf?1711023019=\u0026response-content-disposition=attachment%3B+filename%3DSusceptibility_monitoring_and_the_molecu.pdf\u0026Expires=1732776032\u0026Signature=I6EGpES6flLm8r8HXiyCWnC2aIJumG0dh~~IhqUgMNC~9J88l4HYaliwym61wLrIokgz-kxB3KAOE71Zw8sGmtTK-KvVGfz~18~C-SmmiarOYAwRYksA~JrKI2cTBuQC7HujEG3cnEcKvfP8t-J1jlkuu-bQ2hS94Kw9TlVevu8Kfqd9fbapPt7VnBRwyw39TY3ebt7nlR6GFZhND1dot0kwDwIbaY34OFd~c97HVz6370OMKnQwW6iRP4Na8plZB-ro9M7Ad0z34oBZAN9tkfx9NipI64Ez7whkBl0VfRGg1RQBw-sG1iJk1awyFbOjqGCZ89UaG~mZkds9dyaQ8w__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":286323,"name":"Noctuidae","url":"https://www.academia.edu/Documents/in/Noctuidae"},{"id":295448,"name":"Organophosphate","url":"https://www.academia.edu/Documents/in/Organophosphate"},{"id":764674,"name":"Chlorpyrifos","url":"https://www.academia.edu/Documents/in/Chlorpyrifos"},{"id":845692,"name":"Pyrethroid","url":"https://www.academia.edu/Documents/in/Pyrethroid"},{"id":2021170,"name":"Spodoptera litura","url":"https://www.academia.edu/Documents/in/Spodoptera_litura"}],"urls":[{"id":40491380,"url":"https://doi.org/10.1101/2021.11.17.469006"}]}, 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="116508576"><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/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_"><img alt="Research paper thumbnail of A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)" 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/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_">A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)</a></div><div class="wp-workCard_item"><span>Zoologica Scripta</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdivers...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...</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="116508576"><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="116508576"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508576; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=116508576]").text(description); $(".js-view-count[data-work-id=116508576]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 116508576; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='116508576']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 116508576, 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" } } $('.js-work-strip[data-work-id=116508576]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508576,"title":"A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)","translated_title":"","metadata":{"abstract":"The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...","publisher":"Wiley","publication_name":"Zoologica Scripta"},"translated_abstract":"The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...","internal_url":"https://www.academia.edu/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_","translated_internal_url":"","created_at":"2024-03-21T05:08:53.849-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology"},{"id":27756,"name":"DNA Barcoding","url":"https://www.academia.edu/Documents/in/DNA_Barcoding"},{"id":233017,"name":"Sword","url":"https://www.academia.edu/Documents/in/Sword"}],"urls":[{"id":40491378,"url":"https://onlinelibrary.wiley.com/doi/pdf/10.1111/zsc.12488"}]}, dispatcherData: dispatcherData }); 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Larvae feed on Solanaceae and are very similar to those of other species in the subtribe Mechanitina, with lateral projections on body, one of the main synapomorphies of this subtribe. Based on molecular data, S. k. delicata clustered together with S. karschina karschina, as a monophyletic group sister to the amazon clade of S. reckia. Based on all available data, S. k. delicata is known from only five localities of mid-to high-altitude forests (from 500 to 1000 m of altitude) in northeastern Brazil. 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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="116508571"><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/116508571/A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia"><img alt="Research paper thumbnail of A New Subspecies of Heliconius hermathena (Nymphalidae: Heliconiinae) from Southern Amazonia" class="work-thumbnail" src="https://attachments.academia-assets.com/112619272/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/116508571/A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia">A New Subspecies of Heliconius hermathena (Nymphalidae: Heliconiinae) from Southern Amazonia</a></div><div class="wp-workCard_item"><span>Neotropical Entomology</span><span>, 2018</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="62dd80df351f0281e542cfc2ec2c088d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619272,"asset_id":116508571,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619272/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508571"><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="116508571"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508571; 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This subspecies exhibits a non-mimetic phenotype typical of H. hermathena, but is characterized by the merging of the yellow streak over the forewing cubitus with the red postmedian band in the dorsal forewing. The subspecies is known from two localities in the south of Altamira, Pará State, Brazil, where it inhabits an isolated patch of \"campina\" vegetation more than 600 km from the nearest known H. hermathena populations. Geographic isolation of the population is supported by molecular data; based on the mitochondrial gene COI, all individuals of H. hermathena curua ssp. nov. form a monophyletic group and all haplotypes found in it are unique, suggesting that gene flow is not currently ongoing. Given the fragile situation of Amazonian white sand forests and the proximity of the population to areas of intensive agriculture, this new subspecies and its habitat deserve attention.","publication_date":{"day":null,"month":null,"year":2018,"errors":{}},"publication_name":"Neotropical Entomology","grobid_abstract_attachment_id":112619272},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508571/A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia","translated_internal_url":"","created_at":"2024-03-21T05:08:53.393-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619272,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619272/thumbnails/1.jpg","file_name":"s13744-018-0658-820240321-1-cr3jcf.pdf","download_url":"https://www.academia.edu/attachments/112619272/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"A_New_Subspecies_of_Heliconius_hermathen.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619272/s13744-018-0658-820240321-1-cr3jcf-libre.pdf?1711023013=\u0026response-content-disposition=attachment%3B+filename%3DA_New_Subspecies_of_Heliconius_hermathen.pdf\u0026Expires=1732776032\u0026Signature=XIu5jeT-IIuSUHs2xHtOLpNLvdJfp1GH7Muwn9TeguzSIQyvtjCjYHHzMYbh4Uwmr0zgKVIqNzMeox1lT7uyRcQCkD6D2Q55mD2XzfT7-FRlItV084KfpsBQqABwLKBzoX6ZmLy5nJnfHwAONokcdhzSPLcedHL8lI-DTWU602-dr7ZKRpu9zSEQ-ZoQD3nPPL5HOw32LI265OwRPzduBMmOAhzjZUXYcfu0UWoM~rdk66gi8N-rhqboqkC7qvj0YB-yYrEksKLltdNNXn5PeYqEDhUY8j~2-dauogefrh2dd6CRvauLcFW7FYVU261jodQtxFg-dhG4rI05qDH0FA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia","translated_slug":"","page_count":9,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619272,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619272/thumbnails/1.jpg","file_name":"s13744-018-0658-820240321-1-cr3jcf.pdf","download_url":"https://www.academia.edu/attachments/112619272/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"A_New_Subspecies_of_Heliconius_hermathen.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619272/s13744-018-0658-820240321-1-cr3jcf-libre.pdf?1711023013=\u0026response-content-disposition=attachment%3B+filename%3DA_New_Subspecies_of_Heliconius_hermathen.pdf\u0026Expires=1732776032\u0026Signature=XIu5jeT-IIuSUHs2xHtOLpNLvdJfp1GH7Muwn9TeguzSIQyvtjCjYHHzMYbh4Uwmr0zgKVIqNzMeox1lT7uyRcQCkD6D2Q55mD2XzfT7-FRlItV084KfpsBQqABwLKBzoX6ZmLy5nJnfHwAONokcdhzSPLcedHL8lI-DTWU602-dr7ZKRpu9zSEQ-ZoQD3nPPL5HOw32LI265OwRPzduBMmOAhzjZUXYcfu0UWoM~rdk66gi8N-rhqboqkC7qvj0YB-yYrEksKLltdNNXn5PeYqEDhUY8j~2-dauogefrh2dd6CRvauLcFW7FYVU261jodQtxFg-dhG4rI05qDH0FA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":4313,"name":"Gene Flow","url":"https://www.academia.edu/Documents/in/Gene_Flow"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":51938,"name":"Butterflies","url":"https://www.academia.edu/Documents/in/Butterflies"},{"id":79502,"name":"Amazônia","url":"https://www.academia.edu/Documents/in/Amaz%C3%B4nia"},{"id":373474,"name":"Heliconius","url":"https://www.academia.edu/Documents/in/Heliconius"},{"id":490140,"name":"Monophyly","url":"https://www.academia.edu/Documents/in/Monophyly"},{"id":533119,"name":"Nymphalidae","url":"https://www.academia.edu/Documents/in/Nymphalidae"},{"id":616329,"name":"Subspecies","url":"https://www.academia.edu/Documents/in/Subspecies"},{"id":1317781,"name":"Campina","url":"https://www.academia.edu/Documents/in/Campina"}],"urls":[{"id":40491373,"url":"http://link.springer.com/content/pdf/10.1007/s13744-018-0658-8.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="116508570"><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/116508570/Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_"><img alt="Research paper thumbnail of Evaluation of Anonymous and Expressed Sequence Tag-Derived Polymorphic Microsatellite Markers in the Tobacco Budworm,Heliothis virescens(Lepidoptera: Noctuidae)" class="work-thumbnail" src="https://attachments.academia-assets.com/112619269/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/116508570/Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_">Evaluation of Anonymous and Expressed Sequence Tag-Derived Polymorphic Microsatellite Markers in the Tobacco Budworm,Heliothis virescens(Lepidoptera: Noctuidae)</a></div><div class="wp-workCard_item"><span>Southwestern Entomologist</span><span>, 2011</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c3d983799620dc71dfd8f21a1c476e49" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619269,"asset_id":116508570,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619269/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508570"><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="116508570"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508570; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "c3d983799620dc71dfd8f21a1c476e49" } } $('.js-work-strip[data-work-id=116508570]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508570,"title":"Evaluation of Anonymous and Expressed Sequence Tag-Derived Polymorphic Microsatellite Markers in the Tobacco Budworm,Heliothis virescens(Lepidoptera: Noctuidae)","translated_title":"","metadata":{"publisher":"Society of Southwestern Entomologists","grobid_abstract":"Polymorphic genetic markers were identified and characterized using a partial genomic library of the tobacco budworm, Heliothis virescens (Fabricius), enriched for simple sequence repeats (SSR) and nucleotide sequences of expressed sequence tags (EST). Nucleotide sequences of 192 clones from the partial genomic library yielded 147 unique SSRs while EST evaluations identified 280 SSR-containing sequences. All anonymous SSRs and 192 EST-SSRs were evaluated to select loci that produced the best quality peaks without stutter peaks. Six anonymous markers and nine EST-derived markers were selected to evaluate a sample of 96 insects collected from Stoneville, MS. The observed number of alleles ranged from two to eight, with an average of 5.87 (SE ± 0.53). The polymorphic information content (PIC) value averaged 0.446 (SE ± 0.052). Significant deviations from Hardy-Weinberg expectations were detected at eight loci. We speculate that these loci are under selection in the population of tobacco budworm used in the study. No significant linkage disequilibrium was detected at any of the loci. Proportions of anonymous and EST-SSR markers validated after extensive evaluation were 4.08 and 4.68%, respectively. One anonymous SSR marker (HvMS117) and all nine EST markers were transferable to the bollworm, Helicoverpa zea (Boddie). Resumen. Marcadores genéticos polimórficos fueron identificados y caracterizados usando una biblioteca parcial genómica de Heliothis virescens (Fabricius) que fue enriquecida en repeticiones en secuencia simples (simple sequence repeats [SSR]) y secuencias de nucleótidos de secuencias expresadas (nucleotide sequences of expressed sequence tags [EST]). Las secuencias de nucleótidos de 192 clones de la biblioteca parcial genómica produjeron 147 SSR únicos, mientras que la investigación de los EST identificó 280 secuencias que contenían SSR. Todos los SSR anónimos y los 192 SSR de las EST fueron","publication_date":{"day":null,"month":null,"year":2011,"errors":{}},"publication_name":"Southwestern 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Virescens","url":"https://www.academia.edu/Documents/in/Heliothis_Virescens"}],"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="116508554"><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/116508554/Short_Communication_Development_and_characterization_of_microsatellite_loci_for_genetic_studies_of_the_sugarcane_borer_Diatraea_saccharalis_Lepidoptera_Crambidae_"><img alt="Research paper thumbnail of Short Communication Development and characterization of microsatellite loci for genetic studies of the sugarcane borer, Diatraea saccharalis (Lepidoptera: Crambidae)" class="work-thumbnail" src="https://attachments.academia-assets.com/112619208/thumbnails/1.jpg" /></a></div><div class="wp-workCard 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hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/90440291/Environmental_correlates_of_taxonomic_and_phylogenetic_diversity_in_the_Atlantic_Forest"><img alt="Research paper thumbnail of Environmental correlates of taxonomic and phylogenetic diversity in the Atlantic Forest" class="work-thumbnail" src="https://attachments.academia-assets.com/94003434/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/90440291/Environmental_correlates_of_taxonomic_and_phylogenetic_diversity_in_the_Atlantic_Forest">Environmental correlates of taxonomic and phylogenetic diversity in the Atlantic Forest</a></div><div class="wp-workCard_item"><span>Journal of Biogeography</span><span>, 2021</span></div><div class="wp-workCard_item 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class="work-thumbnail" src="https://attachments.academia-assets.com/94003433/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/90440290/Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift">Use of host plants by Troidini butterflies (Papilionidae, Papilioninae): constraints on host shift</a></div><div class="wp-workCard_item"><span>Biological Journal of the Linnean Society</span><span>, 2007</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="86892dc5c094124b9ad2ffa28bff900d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" 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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: "86892dc5c094124b9ad2ffa28bff900d" } } $('.js-work-strip[data-work-id=90440290]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":90440290,"title":"Use of host plants by Troidini butterflies (Papilionidae, Papilioninae): constraints on host shift","translated_title":"","metadata":{"publisher":"Oxford University Press (OUP)","grobid_abstract":"Molecular phylogenetic analyses were conducted to determine relationships and to investigate character evolution for the Troidini/ Aristolochia interaction, in an attempt to answer the following questions: (1) what is the present pattern of use of Aristolochia by these butterflies; (2) is the pattern we see today related to the phylogeny of plants or to their chemical composition; (3) can the geographical distribution of Aristolochia explain the host plant use observed today; and (4) how did the interaction between Troidini and Aristolochia evolve? Analyses of character optimization suggest that the current pattern of host plant use of these butterflies does not seem to be constrained by the phylogeny of their food plants, neither by the secondary chemicals in these plants nor by their geographical similarity. The current host plant use in these butterflies seems to be simply opportunistic, with species with a wider geographical range using more species of host plants than those with a more restricted distribution.","publication_date":{"day":null,"month":null,"year":2007,"errors":{}},"publication_name":"Biological Journal of the Linnean Society","grobid_abstract_attachment_id":94003433},"translated_abstract":null,"internal_url":"https://www.academia.edu/90440290/Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift","translated_internal_url":"","created_at":"2022-11-10T03:28:43.005-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":94003433,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/94003433/thumbnails/1.jpg","file_name":"j.1095-8312.2007.00727.x.pdf","download_url":"https://www.academia.edu/attachments/94003433/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Use_of_host_plants_by_Troidini_butterfli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/94003433/j.1095-8312.2007.00727.x-libre.pdf?1668095573=\u0026response-content-disposition=attachment%3B+filename%3DUse_of_host_plants_by_Troidini_butterfli.pdf\u0026Expires=1732776032\u0026Signature=U~eizskxLeeNvosQgI0k0EW7bgw1Ufa77xT1egR5KdNLF5eILqYadFKX4oCSGl3~YZbPy9Yj-MZZRNRbphTqQ3Kw2P6egva6vQmMJobkS5pN0ZYQ7yuTJeGij3xnXrLywqojIh-UPSlncLeO2ojONHcTo2iTCSKI~XMxhDhoEuuG~z5Ufb~muwVmR1GKewtOpcrX2oCdlFvXTzYFmusupioJoUCT4GK82Vq01UoS4yD4bigtH1s8d2CTCt~UNdW5bSqCCNrGU47ok1NM~AKyTGM6NzpXqgsEOqSgStUWSx1C~tA8eT7D6xuxSnCcdia2Ns7RbRvNwfFeP5jsAPuxgw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift","translated_slug":"","page_count":15,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":94003433,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/94003433/thumbnails/1.jpg","file_name":"j.1095-8312.2007.00727.x.pdf","download_url":"https://www.academia.edu/attachments/94003433/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Use_of_host_plants_by_Troidini_butterfli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/94003433/j.1095-8312.2007.00727.x-libre.pdf?1668095573=\u0026response-content-disposition=attachment%3B+filename%3DUse_of_host_plants_by_Troidini_butterfli.pdf\u0026Expires=1732776032\u0026Signature=U~eizskxLeeNvosQgI0k0EW7bgw1Ufa77xT1egR5KdNLF5eILqYadFKX4oCSGl3~YZbPy9Yj-MZZRNRbphTqQ3Kw2P6egva6vQmMJobkS5pN0ZYQ7yuTJeGij3xnXrLywqojIh-UPSlncLeO2ojONHcTo2iTCSKI~XMxhDhoEuuG~z5Ufb~muwVmR1GKewtOpcrX2oCdlFvXTzYFmusupioJoUCT4GK82Vq01UoS4yD4bigtH1s8d2CTCt~UNdW5bSqCCNrGU47ok1NM~AKyTGM6NzpXqgsEOqSgStUWSx1C~tA8eT7D6xuxSnCcdia2Ns7RbRvNwfFeP5jsAPuxgw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":1302079,"name":"Host Plant","url":"https://www.academia.edu/Documents/in/Host_Plant"},{"id":1569877,"name":"Host Shift","url":"https://www.academia.edu/Documents/in/Host_Shift"}],"urls":[]}, dispatcherData: dispatcherData }); 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AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within populations. Clustering analyzes also indicated low genetic differentiation. The haplotype network obtained with combined datasets resulted in 35 haplotypes, with 28 exclusive occurrences, four of them sampled only from soybean fields. The minimum spanning network showed star-shaped structures typical of populations that underwent a recent demographic expansion. The recent expansion was supported by other demographic analyzes, such as the Bayesian skyline plot, the unimodal distribution of paired differences among mitochondr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6044a4595ee7345addafc520eeac8bac" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":94002110,"asset_id":90438463,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/94002110/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="90438463"><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="90438463"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 90438463; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=90438463]").text(description); $(".js-view-count[data-work-id=90438463]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 90438463; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='90438463']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 90438463, 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: "6044a4595ee7345addafc520eeac8bac" } } $('.js-work-strip[data-work-id=90438463]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":90438463,"title":"Genetic variability and demographic history ofHeliothis virescens(Lepidoptera: Noctuidae) populations from Brazil inferred by mtDNA sequences","translated_title":"","metadata":{"abstract":"Intra- and inter-population genetic variability and the demographic history ofHeliothis virescens(F.) populations were evaluated by using mtDNA markers (coxI, coxIIandnad6) with samples from the major cotton- and soybean-producing regions in Brazil in the growing seasons 2007/08, 2008/09 and 2009/10. AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within populations. Clustering analyzes also indicated low genetic differentiation. The haplotype network obtained with combined datasets resulted in 35 haplotypes, with 28 exclusive occurrences, four of them sampled only from soybean fields. The minimum spanning network showed star-shaped structures typical of populations that underwent a recent demographic expansion. The recent expansion was supported by other demographic analyzes, such as the Bayesian skyline plot, the unimodal distribution of paired differences among mitochondr...","publisher":"Cambridge University Press (CUP)","ai_title_tag":"Genetic Variability and Demographic History of Heliothis virescens in Brazil","publication_date":{"day":null,"month":null,"year":2011,"errors":{}},"publication_name":"Bulletin of Entomological Research"},"translated_abstract":"Intra- and inter-population genetic variability and the demographic history ofHeliothis virescens(F.) populations were evaluated by using mtDNA markers (coxI, coxIIandnad6) with samples from the major cotton- and soybean-producing regions in Brazil in the growing seasons 2007/08, 2008/09 and 2009/10. AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within 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="81448372"><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/81448372/Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations"><img alt="Research paper thumbnail of Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations" 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/81448372/Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations">Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.&#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. Our study exemplifies the difficulty of testing hypotheses of divergence times and of choosing between alternative dating scenarios, and shows that age estimates based on seemingly plausible calibrations may be grossly incongruent</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="81448372"><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="81448372"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 81448372; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=81448372]").text(description); $(".js-view-count[data-work-id=81448372]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 81448372; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='81448372']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 81448372, 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" } } $('.js-work-strip[data-work-id=81448372]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":81448372,"title":"Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations","translated_title":"","metadata":{"abstract":"The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.\u0026#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. Our study exemplifies the difficulty of testing hypotheses of divergence times and of choosing between alternative dating scenarios, and shows that age estimates based on seemingly plausible calibrations may be grossly incongruent","publisher":"Dryad Digital Repository","publication_date":{"day":null,"month":null,"year":2015,"errors":{}}},"translated_abstract":"The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.\u0026#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. Our study exemplifies the difficulty of testing hypotheses of divergence times and of choosing between alternative dating scenarios, and shows that age estimates based on seemingly plausible calibrations may be grossly incongruent","internal_url":"https://www.academia.edu/81448372/Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations","translated_internal_url":"","created_at":"2022-06-14T01:10:14.128-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[],"research_interests":[{"id":85683,"name":"Molecular clock","url":"https://www.academia.edu/Documents/in/Molecular_clock"},{"id":110204,"name":"Dating","url":"https://www.academia.edu/Documents/in/Dating"},{"id":141838,"name":"Herbivory","url":"https://www.academia.edu/Documents/in/Herbivory"}],"urls":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="6702319" id="papers"><div class="js-work-strip profile--work_container" data-work-id="116508592"><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/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_"><img alt="Research paper thumbnail of Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]" class="work-thumbnail" src="https://attachments.academia-assets.com/112619273/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/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_">Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]</a></div><div class="wp-workCard_item"><span>Scopus</span><span>, 2009</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="d378225a0ee584ccdbdaf0d41eada6b1" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619273,"asset_id":116508592,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619273/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508592"><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="116508592"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508592; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=116508592]").text(description); $(".js-view-count[data-work-id=116508592]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 116508592; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='116508592']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 116508592, 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: "d378225a0ee584ccdbdaf0d41eada6b1" } } $('.js-work-strip[data-work-id=116508592]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508592,"title":"Barcoding Lepidoptera: Current Situation And Perspectives On The Usefulness Of A Contentious Technique [barcoding Lepidoptera: Situação Atual E Perspectivas Sobre A Utilidade De Uma Técnica Controversa]","translated_title":"","metadata":{"publisher":"Institute of Electrical and Electronics Engineers","grobid_abstract":"Barcoding Lepidoptera: Situação Atual e Perspectivas sobre a Utilidade de uma Técnica Controversa RESUMO-A necessidade crescente de identificação e delimitação de novas espécies, ou de espécies crípticas já estabelecidas, que estão sendo perdidas a uma taxa também crescente, tem levado diversos especialistas a utilizarem uma variedade de ferramentas moleculares e computacionais. Neste momento, taxonomistas devem estar atentos a toda nova tecnologia disponível na chamada \"revolução dirigida pela tecnologia\" na sistemática, que tem entre as novas ferramentas moleculares a utilização de \"DNA barcodes\". O uso de \"DNA barcode\" tem sido amplamente discutido por aqueles que aplicam essa abordagem com sucesso para identificar e diagnosticar espécies, e por aqueles que acreditam que são tantos os problemas no uso desse marcador molecular que não se justifica seu emprego. Para insetos da ordem Lepidoptera nenhum lado parece estar totalmente certo ou errado e, embora alguns grupos de lepidópteros tenham sido resolvidos taxonomicamente pelo uso exclusivo ou adicional desse marcador, para outros o \"barcode\" ajudou pouco a resolver problemas taxonômicos. Aqui nós apresentamos brevemente prós e contras do uso de \"DNA barcode\" como ferramenta em estudos taxonômicos, com atenção especial para estudos com grupos de Lepidoptera desenvolvidos nos últimos anos.","publication_date":{"day":null,"month":null,"year":2009,"errors":{}},"publication_name":"Scopus","grobid_abstract_attachment_id":112619273},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508592/Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situa%C3%A7%C3%A3o_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_T%C3%A9cnica_Controversa_","translated_internal_url":"","created_at":"2024-03-21T05:08:55.351-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619273,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619273/thumbnails/1.jpg","file_name":"s1519-566x200900040000120240321-1-tgntxx.pdf","download_url":"https://www.academia.edu/attachments/112619273/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Barcoding_Lepidoptera_Current_Situation.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619273/s1519-566x200900040000120240321-1-tgntxx-libre.pdf?1711023089=\u0026response-content-disposition=attachment%3B+filename%3DBarcoding_Lepidoptera_Current_Situation.pdf\u0026Expires=1732776032\u0026Signature=gXHkosW3bSfxlQQEs4s0TYctaJAZpMh1V0SkjjIqNMdnsN4PfCnUs-F7PIhHBWyL-YiUtJSfExtaztFVvrjGUwfX3lV9pxbvkcVwiWsZhDTIGpPkhYz5HpN-7h35hQ~eoboWJUz9pe7XBPLoIt0DPN1YjiIL-O-oQ4WgQNYnmM3~W9ZjH2xNaAfHdyraP81UXTBnlbxMdamRo~kYjSjQrjWl591ZJ-~gJiQ4hi0WV~IxIMQivrg7haN1QAJdpcGgsAREqv6KIEubAvdYpnT1oKk3QPMEZhUZ9crTR3ohfPu4f6FjzmMKfl5XXUNJsKmIPSqhB6Adb6G64mJNf0R87A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Barcoding_Lepidoptera_Current_Situation_And_Perspectives_On_The_Usefulness_Of_A_Contentious_Technique_barcoding_Lepidoptera_Situação_Atual_E_Perspectivas_Sobre_A_Utilidade_De_Uma_Técnica_Controversa_","translated_slug":"","page_count":11,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619273,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619273/thumbnails/1.jpg","file_name":"s1519-566x200900040000120240321-1-tgntxx.pdf","download_url":"https://www.academia.edu/attachments/112619273/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Barcoding_Lepidoptera_Current_Situation.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619273/s1519-566x200900040000120240321-1-tgntxx-libre.pdf?1711023089=\u0026response-content-disposition=attachment%3B+filename%3DBarcoding_Lepidoptera_Current_Situation.pdf\u0026Expires=1732776032\u0026Signature=gXHkosW3bSfxlQQEs4s0TYctaJAZpMh1V0SkjjIqNMdnsN4PfCnUs-F7PIhHBWyL-YiUtJSfExtaztFVvrjGUwfX3lV9pxbvkcVwiWsZhDTIGpPkhYz5HpN-7h35hQ~eoboWJUz9pe7XBPLoIt0DPN1YjiIL-O-oQ4WgQNYnmM3~W9ZjH2xNaAfHdyraP81UXTBnlbxMdamRo~kYjSjQrjWl591ZJ-~gJiQ4hi0WV~IxIMQivrg7haN1QAJdpcGgsAREqv6KIEubAvdYpnT1oKk3QPMEZhUZ9crTR3ohfPu4f6FjzmMKfl5XXUNJsKmIPSqhB6Adb6G64mJNf0R87A__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":422,"name":"Computer Science","url":"https://www.academia.edu/Documents/in/Computer_Science"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":27756,"name":"DNA Barcoding","url":"https://www.academia.edu/Documents/in/DNA_Barcoding"},{"id":31356,"name":"Lepidoptera","url":"https://www.academia.edu/Documents/in/Lepidoptera"},{"id":106145,"name":"Classification","url":"https://www.academia.edu/Documents/in/Classification"},{"id":247162,"name":"Scopus","url":"https://www.academia.edu/Documents/in/Scopus"}],"urls":[{"id":40491394,"url":"http://repositorio.unicamp.br/jspui/bitstream/REPOSIP/91891/1/2-s2.0-70349976028.pdf"}]}, dispatcherData: dispatcherData }); 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Reports on field-evolved resistance of lepidopteran pests to chitin synthesis inhibitors and the selection of laboratory resistant strains to these products require a detailed investigation on the resistance mechanisms and on the identification of molecular markers to support the implementation of efficient monitoring and resistance management programs. Teflubenzuron is a chitin synthesis inhibitor highly effective in controlling lepidopteran pests, including nowadays the world widely distributed fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith, 1797) (Lepidoptera: Noctuidae). We report the selection of a laboratory strain of S. frugiperda resistant to teflubenzuron, and its use for the characterization of the inheritance of resistance, evaluation of cross-resistance to other chitin-synthesis inhibitors and the identification of a set of single nucleotide polymorphisms (SNPs) for use as candidate molecular markers for monitoring the evolution of resistance of S. frugiperda to teflubenzuron. The resistance of the selected strain of S. frugiperda to teflubenzuron was characterized as polygenic, autosomal, and incompletely recessive. The resistance ratio observed was nearly 1,365-fold. Teflubenzuron-resistant strain showed some cross-resistance to lufenuron and novaluron but not to chlorfluazuron. We also detected a set of 72 SNPs that could support monitoring of the resistance frequency to teflubenzuron in field populations. Our data contribute to the understanding of the resistance mechanisms and the inheritance of polygenic resistance of S. frugiperda to benzoylureas. We also contribute with candidate markers as tools for monitoring the emergence and spread of teflubenzuron resistance in S. frugiperda.","publication_date":{"day":17,"month":4,"year":2021,"errors":{}},"publication_name":"Journal of Pest 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widespread through the Americas, from Argentina to the southern United States of America. All eight recognized species within Hermeuptychia are small and brown, with very similar interspecific external morphologies and intraspecifically variable ocelli patterns that render taxonomic identification based on morphology difficult. In our study, we surveyed variability within Hermeuptychia, and evaluate species boundaries based on molecular data (sequences of the \"barcode\" mitochondrial DNA COI gene) and morphology (mainly male genitalia), using a phylogenetic approach. We found eight DNA-based and twelve morphological groups in our sampling. Species names were assigned based mainly on comparisons with male genitalia morphology descriptions corresponding to name-bearing type specimens. Morphological and DNA variability were highly congruent, with the exception of group H, the H. cucullina complex. Also, the barcode region showed a clear threshold for intra and interspecific mean distances around 2%. Based on these results we circumscribe the species boundaries in the genus Hermeuptychia, and discuss conflicts between mitochondrial genes and classic morphological approaches for identifying and delimiting species. Our study revealed cryptic diversity within a ubiquitous genus of Neotropical butterflies.","publication_date":{"day":6,"month":9,"year":2013,"errors":{}},"publication_name":"Molecular Ecology 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Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":27756,"name":"DNA Barcoding","url":"https://www.academia.edu/Documents/in/DNA_Barcoding"},{"id":31356,"name":"Lepidoptera","url":"https://www.academia.edu/Documents/in/Lepidoptera"},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":51938,"name":"Butterflies","url":"https://www.academia.edu/Documents/in/Butterflies"},{"id":54433,"name":"Phylogeny","url":"https://www.academia.edu/Documents/in/Phylogeny"},{"id":63093,"name":"Mitochondrial DNA","url":"https://www.academia.edu/Documents/in/Mitochondrial_DNA"},{"id":83402,"name":"Americas","url":"https://www.academia.edu/Documents/in/Americas"},{"id":131237,"name":"Cluster 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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="116508587"><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/116508587/Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos"><img alt="Research paper thumbnail of Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of <i>Spodoptera frugiperda</i> to lambda‐cyhalothrin and chlorpyrifos" 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/116508587/Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos">Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of <i>Spodoptera frugiperda</i> to lambda‐cyhalothrin and chlorpyrifos</a></div><div class="wp-workCard_item"><span>Pest Management Science</span><span>, Mar 1, 2023</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several reco...</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">BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.</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="116508587"><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="116508587"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508587; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=116508587]").text(description); $(".js-view-count[data-work-id=116508587]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 116508587; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='116508587']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 116508587, 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" } } $('.js-work-strip[data-work-id=116508587]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508587,"title":"Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of \u003ci\u003eSpodoptera frugiperda\u003c/i\u003e to lambda‐cyhalothrin and chlorpyrifos","translated_title":"","metadata":{"abstract":"BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.","publisher":"Wiley","publication_date":{"day":1,"month":3,"year":2023,"errors":{}},"publication_name":"Pest Management Science"},"translated_abstract":"BACKGROUNDSpodoptera frugiperda (J. E. Smith) is a widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda‐cyhalothrin (pyrethroid). Here, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda‐cyhalothrin (197 populations) collected from major maize‐growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of laboratory‐selected, chlorpyrifos‐ and lambda‐cyhalothrin‐resistant strains to a susceptible reference strain (Sf‐ss) of S. frugiperda.RESULTSThe susceptibility monitoring detected average survival ranging from 29.3% to 36.0% for chlorpyrifos, and 23.1% to 68.0% for lambda‐cyhalothrin. The resistance ratio of the chlorpyrifos‐resistant strain (Clo‐rr) was 25.4‐fold and of the lambda‐cyhalothrin‐resistant strain (Lam‐rr) was 21.5‐fold. We identified 1098 differentially expressed genes (DEGs) between Clo‐rr and Sf‐ss, and 303 DEGs between Lam‐rr and Sf‐ss. Functional analyses of the DEGs revealed the up‐regulation of several detoxification enzymes, mainly cytochrome P450 belonging to CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box class O (FoxO) transcription factor were also up‐regulated. Variant analysis of target‐site mutations for both pesticides identified the A201S and F290V mutations in acetylcholinesterase‐1, both occurring in heterozigosis in the Clo‐rr S. frugiperda strain.CONCLUSIONOur data show that the overexpression of the enzymatic detoxification machinery is the main difference to explain the resistance of Clo‐rr and Lam‐rr strains of S. frugiperda to chlorpyrifos and lambda‐cyhalothrin, although a target‐site mutation also contributes to the Clo‐rr resistance to chlorpyrifos. © 2023 Society of Chemical Industry.","internal_url":"https://www.academia.edu/116508587/Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos","translated_internal_url":"","created_at":"2024-03-21T05:08:54.871-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"Susceptibility_monitoring_and_comparative_gene_expression_of_susceptible_and_resistant_strains_of_i_Spodoptera_frugiperda_i_to_lambda_cyhalothrin_and_chlorpyrifos","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":295448,"name":"Organophosphate","url":"https://www.academia.edu/Documents/in/Organophosphate"},{"id":764674,"name":"Chlorpyrifos","url":"https://www.academia.edu/Documents/in/Chlorpyrifos"},{"id":845692,"name":"Pyrethroid","url":"https://www.academia.edu/Documents/in/Pyrethroid"},{"id":1279211,"name":"Pest Management Science","url":"https://www.academia.edu/Documents/in/Pest_Management_Science"},{"id":1957240,"name":"ENVIRONMENTAL SCIENCE AND MANAGEMENT","url":"https://www.academia.edu/Documents/in/ENVIRONMENTAL_SCIENCE_AND_MANAGEMENT"},{"id":2021170,"name":"Spodoptera litura","url":"https://www.academia.edu/Documents/in/Spodoptera_litura"}],"urls":[{"id":40491389,"url":"https://doi.org/10.1002/ps.7399"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="116508585"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/116508585/Systematic_Position_Immature_Stages_and_Geographic_Distribution_of_Glennia_pylotis_Godart_1819_Lepidoptera_Papilionoidea_Pieridae_"><img alt="Research paper thumbnail of Systematic Position, Immature Stages, and Geographic Distribution of Glennia pylotis (Godart, 1819) (Lepidoptera: Papilionoidea: Pieridae)" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard 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$(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="116508580"><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/116508580/Genetic_Diversity_of_Paryphthimoides_poltys_Nymphalidae_Satyrinae_Euptychiina_in_a_Fragmented_Agricultural_Landscape_in_the_Brazilian_Atlantic_Forest"><img alt="Research paper thumbnail of Genetic Diversity of Paryphthimoides poltys (Nymphalidae: Satyrinae: Euptychiina) in a Fragmented Agricultural Landscape in the Brazilian Atlantic Forest" 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/116508580/Genetic_Diversity_of_Paryphthimoides_poltys_Nymphalidae_Satyrinae_Euptychiina_in_a_Fragmented_Agricultural_Landscape_in_the_Brazilian_Atlantic_Forest">Genetic Diversity of Paryphthimoides poltys (Nymphalidae: Satyrinae: Euptychiina) in a Fragmented Agricultural Landscape in the Brazilian Atlantic Forest</a></div><div class="wp-workCard_item"><span>Journal of the Lepidopterists' Society</span><span>, Nov 22, 2022</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="116508580"><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="116508580"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508580; 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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="116508578"><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/116508578/Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos"><img alt="Research paper thumbnail of Susceptibility monitoring and the molecular characterization of resistance of Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin and chlorpyrifos" class="work-thumbnail" src="https://attachments.academia-assets.com/112619268/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/116508578/Susceptibility_monitoring_and_the_molecular_characterization_of_resistance_of_Spodoptera_frugiperda_Lepidoptera_Noctuidae_to_lambda_cyhalothrin_and_chlorpyrifos">Susceptibility monitoring and the molecular characterization of resistance of Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin and chlorpyrifos</a></div><div class="wp-workCard_item"><span>bioRxiv (Cold Spring Harbor Laboratory)</span><span>, Nov 19, 2021</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="1a9bd4ff98576370162f985faceb634c" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619268,"asset_id":116508578,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619268/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508578"><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="116508578"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508578; 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E. Smith) is a serious and widespread agricultural pest with several records of resistance to different insecticides and Bt proteins, including the neurotoxic insecticides chlorpyrifos (organophosphate) and lambda-cyhalothrin (pyrethroid). In this study, we (i) characterized and monitored the susceptibility of field populations of S. frugiperda to chlorpyrifos (194 populations) and lambda-cyhalothrin (197 populations) collected from major maize-growing regions of Brazil from 2003 to 2016, and (ii) compared gene expression levels of chlorpyrifos-and lambda-cyhalothrin-resistant strains to a susceptible reference strain (Sfss) of S. frugiperda. Laboratory-guided assays to monitor larval susceptibility detected average survival ranging from 29.3% to 36.0% to chlorpyrifos, and 23.1% to 68.0% to lambdacyhalothrin at diagnostic concentration, based on LC99 of the susceptible reference strain of each insecticide. The resistance ratio of the chlorpyrifos-resistant strain (Clo-rr) was 25.4-fold and of the lambda-cyhalothrin-resistant strain (Lam-rr) was 217-fold. Differential gene expression analyses between resistant vs susceptible strains identified 1,098 differentially expressed genes (DEGs) between Clo-rr and Sf-ss, and 303 DEGs between Lam-rr and Sf-ss. Functional analyses of the DEGs revealed the up-regulation of several detoxification enzymes, mainly cytochrome P450 belonging to the CYP3 and CYP6 clans. Genes associated with regulatory processes, such as the forkhead box O (FoxO) were also up-regulated. 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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="116508576"><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/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_"><img alt="Research paper thumbnail of A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)" 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/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_">A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)</a></div><div class="wp-workCard_item"><span>Zoologica Scripta</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdivers...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...</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="116508576"><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="116508576"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508576; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=116508576]").text(description); $(".js-view-count[data-work-id=116508576]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 116508576; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='116508576']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 116508576, 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" } } $('.js-work-strip[data-work-id=116508576]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":116508576,"title":"A double‐edged sword: Unrecognized cryptic diversity and taxonomic impediment in Eois (Lepidoptera, Geometridae)","translated_title":"","metadata":{"abstract":"The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...","publisher":"Wiley","publication_name":"Zoologica Scripta"},"translated_abstract":"The genus Eois Hübner (Geometridae: Larentiinae) comprises 254 valid species. Being a hyperdiverse genus, Eois potentially includes many undescribed cryptic species and embodies a problematic taxonomic scenario. The actual diversity of Eois is greatly underestimated and the Neotropical fauna needs to be well known since it figures as one of the most threatened terrestrial ecosystem. In the present study, we compare three species delimitation methods to highlight the hidden diversity within a subset of Eois species: Automatic Barcode Gap Discovery, Bayesian Poisson Tree Processes and Multi‐Rate Poisson Tree Processes. Our results point to an increase up to 176% in the currently valid species number. The hypothesis of cryptic diversity is corroborated by morphological characters within some species complexes. For complexes comprising species of Brazilian fauna, we provide a preliminary taxonomic assessment. Additionally, we found no congruence among the three delimitation methods for ...","internal_url":"https://www.academia.edu/116508576/A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_","translated_internal_url":"","created_at":"2024-03-21T05:08:53.849-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[],"slug":"A_double_edged_sword_Unrecognized_cryptic_diversity_and_taxonomic_impediment_in_Eois_Lepidoptera_Geometridae_","translated_slug":"","page_count":null,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[],"research_interests":[{"id":155,"name":"Evolutionary Biology","url":"https://www.academia.edu/Documents/in/Evolutionary_Biology"},{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology"},{"id":27756,"name":"DNA Barcoding","url":"https://www.academia.edu/Documents/in/DNA_Barcoding"},{"id":233017,"name":"Sword","url":"https://www.academia.edu/Documents/in/Sword"}],"urls":[{"id":40491378,"url":"https://onlinelibrary.wiley.com/doi/pdf/10.1111/zsc.12488"}]}, dispatcherData: dispatcherData }); 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Larvae feed on Solanaceae and are very similar to those of other species in the subtribe Mechanitina, with lateral projections on body, one of the main synapomorphies of this subtribe. Based on molecular data, S. k. delicata clustered together with S. karschina karschina, as a monophyletic group sister to the amazon clade of S. reckia. Based on all available data, S. k. delicata is known from only five localities of mid-to high-altitude forests (from 500 to 1000 m of altitude) in northeastern Brazil. 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This subspecies exhibits a non-mimetic phenotype typical of H. hermathena, but is characterized by the merging of the yellow streak over the forewing cubitus with the red postmedian band in the dorsal forewing. The subspecies is known from two localities in the south of Altamira, Pará State, Brazil, where it inhabits an isolated patch of \"campina\" vegetation more than 600 km from the nearest known H. hermathena populations. Geographic isolation of the population is supported by molecular data; based on the mitochondrial gene COI, all individuals of H. hermathena curua ssp. nov. form a monophyletic group and all haplotypes found in it are unique, suggesting that gene flow is not currently ongoing. Given the fragile situation of Amazonian white sand forests and the proximity of the population to areas of intensive agriculture, this new subspecies and its habitat deserve attention.","publication_date":{"day":null,"month":null,"year":2018,"errors":{}},"publication_name":"Neotropical Entomology","grobid_abstract_attachment_id":112619272},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508571/A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia","translated_internal_url":"","created_at":"2024-03-21T05:08:53.393-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619272,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619272/thumbnails/1.jpg","file_name":"s13744-018-0658-820240321-1-cr3jcf.pdf","download_url":"https://www.academia.edu/attachments/112619272/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"A_New_Subspecies_of_Heliconius_hermathen.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619272/s13744-018-0658-820240321-1-cr3jcf-libre.pdf?1711023013=\u0026response-content-disposition=attachment%3B+filename%3DA_New_Subspecies_of_Heliconius_hermathen.pdf\u0026Expires=1732776032\u0026Signature=XIu5jeT-IIuSUHs2xHtOLpNLvdJfp1GH7Muwn9TeguzSIQyvtjCjYHHzMYbh4Uwmr0zgKVIqNzMeox1lT7uyRcQCkD6D2Q55mD2XzfT7-FRlItV084KfpsBQqABwLKBzoX6ZmLy5nJnfHwAONokcdhzSPLcedHL8lI-DTWU602-dr7ZKRpu9zSEQ-ZoQD3nPPL5HOw32LI265OwRPzduBMmOAhzjZUXYcfu0UWoM~rdk66gi8N-rhqboqkC7qvj0YB-yYrEksKLltdNNXn5PeYqEDhUY8j~2-dauogefrh2dd6CRvauLcFW7FYVU261jodQtxFg-dhG4rI05qDH0FA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"A_New_Subspecies_of_Heliconius_hermathena_Nymphalidae_Heliconiinae_from_Southern_Amazonia","translated_slug":"","page_count":9,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619272,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619272/thumbnails/1.jpg","file_name":"s13744-018-0658-820240321-1-cr3jcf.pdf","download_url":"https://www.academia.edu/attachments/112619272/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"A_New_Subspecies_of_Heliconius_hermathen.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619272/s13744-018-0658-820240321-1-cr3jcf-libre.pdf?1711023013=\u0026response-content-disposition=attachment%3B+filename%3DA_New_Subspecies_of_Heliconius_hermathen.pdf\u0026Expires=1732776032\u0026Signature=XIu5jeT-IIuSUHs2xHtOLpNLvdJfp1GH7Muwn9TeguzSIQyvtjCjYHHzMYbh4Uwmr0zgKVIqNzMeox1lT7uyRcQCkD6D2Q55mD2XzfT7-FRlItV084KfpsBQqABwLKBzoX6ZmLy5nJnfHwAONokcdhzSPLcedHL8lI-DTWU602-dr7ZKRpu9zSEQ-ZoQD3nPPL5HOw32LI265OwRPzduBMmOAhzjZUXYcfu0UWoM~rdk66gi8N-rhqboqkC7qvj0YB-yYrEksKLltdNNXn5PeYqEDhUY8j~2-dauogefrh2dd6CRvauLcFW7FYVU261jodQtxFg-dhG4rI05qDH0FA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":4313,"name":"Gene Flow","url":"https://www.academia.edu/Documents/in/Gene_Flow"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine"},{"id":51938,"name":"Butterflies","url":"https://www.academia.edu/Documents/in/Butterflies"},{"id":79502,"name":"Amazônia","url":"https://www.academia.edu/Documents/in/Amaz%C3%B4nia"},{"id":373474,"name":"Heliconius","url":"https://www.academia.edu/Documents/in/Heliconius"},{"id":490140,"name":"Monophyly","url":"https://www.academia.edu/Documents/in/Monophyly"},{"id":533119,"name":"Nymphalidae","url":"https://www.academia.edu/Documents/in/Nymphalidae"},{"id":616329,"name":"Subspecies","url":"https://www.academia.edu/Documents/in/Subspecies"},{"id":1317781,"name":"Campina","url":"https://www.academia.edu/Documents/in/Campina"}],"urls":[{"id":40491373,"url":"http://link.springer.com/content/pdf/10.1007/s13744-018-0658-8.pdf"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="116508570"><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/116508570/Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_"><img alt="Research paper thumbnail of Evaluation of Anonymous and Expressed Sequence Tag-Derived Polymorphic Microsatellite Markers in the Tobacco Budworm,Heliothis virescens(Lepidoptera: Noctuidae)" class="work-thumbnail" src="https://attachments.academia-assets.com/112619269/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/116508570/Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_">Evaluation of Anonymous and Expressed Sequence Tag-Derived Polymorphic Microsatellite Markers in the Tobacco Budworm,Heliothis virescens(Lepidoptera: Noctuidae)</a></div><div class="wp-workCard_item"><span>Southwestern Entomologist</span><span>, 2011</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="c3d983799620dc71dfd8f21a1c476e49" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":112619269,"asset_id":116508570,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/112619269/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="116508570"><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="116508570"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 116508570; 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Nucleotide sequences of 192 clones from the partial genomic library yielded 147 unique SSRs while EST evaluations identified 280 SSR-containing sequences. All anonymous SSRs and 192 EST-SSRs were evaluated to select loci that produced the best quality peaks without stutter peaks. Six anonymous markers and nine EST-derived markers were selected to evaluate a sample of 96 insects collected from Stoneville, MS. The observed number of alleles ranged from two to eight, with an average of 5.87 (SE ± 0.53). The polymorphic information content (PIC) value averaged 0.446 (SE ± 0.052). Significant deviations from Hardy-Weinberg expectations were detected at eight loci. We speculate that these loci are under selection in the population of tobacco budworm used in the study. No significant linkage disequilibrium was detected at any of the loci. Proportions of anonymous and EST-SSR markers validated after extensive evaluation were 4.08 and 4.68%, respectively. One anonymous SSR marker (HvMS117) and all nine EST markers were transferable to the bollworm, Helicoverpa zea (Boddie). Resumen. Marcadores genéticos polimórficos fueron identificados y caracterizados usando una biblioteca parcial genómica de Heliothis virescens (Fabricius) que fue enriquecida en repeticiones en secuencia simples (simple sequence repeats [SSR]) y secuencias de nucleótidos de secuencias expresadas (nucleotide sequences of expressed sequence tags [EST]). Las secuencias de nucleótidos de 192 clones de la biblioteca parcial genómica produjeron 147 SSR únicos, mientras que la investigación de los EST identificó 280 secuencias que contenían SSR. Todos los SSR anónimos y los 192 SSR de las EST fueron","publication_date":{"day":null,"month":null,"year":2011,"errors":{}},"publication_name":"Southwestern Entomologist","grobid_abstract_attachment_id":112619269},"translated_abstract":null,"internal_url":"https://www.academia.edu/116508570/Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_","translated_internal_url":"","created_at":"2024-03-21T05:08:53.270-07:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":112619269,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619269/thumbnails/1.jpg","file_name":"059.036.030620240321-1-fyehio.pdf","download_url":"https://www.academia.edu/attachments/112619269/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Evaluation_of_Anonymous_and_Expressed_Se.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619269/059.036.030620240321-1-fyehio-libre.pdf?1711023008=\u0026response-content-disposition=attachment%3B+filename%3DEvaluation_of_Anonymous_and_Expressed_Se.pdf\u0026Expires=1732776032\u0026Signature=ELBaBOwbI7meAHvi4zrCqjcpEOtqFW1tu8ukJcYDx45ZIahGfDTbCJosjyHwejPNE5LVDUVG8BPc513AMtAa4MidR7boxgeh3TL9FQyHiZX60mk5I8CMPRHNgmCP~-Ij5OxroO1kJlt322Tnp9ziJt8-mXj5ipsHynNq54mYAjWItnf2SWF3PLkTXTkKrcYBwB5obLRYcQ07-7TopbPNfDdq1EF~ZJlm1i0ikRaZ2V7pORSwBBnqhHtoBojykDmoTT-khHeuug86nh9aJAi51rf7SNFel0PYP1gk7tJTfdbqWSFt6K4xKbvWit31qo9lTeP~nyv4ffPDWZm2WyHy8Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Evaluation_of_Anonymous_and_Expressed_Sequence_Tag_Derived_Polymorphic_Microsatellite_Markers_in_the_Tobacco_Budworm_Heliothis_virescens_Lepidoptera_Noctuidae_","translated_slug":"","page_count":9,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":112619269,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/112619269/thumbnails/1.jpg","file_name":"059.036.030620240321-1-fyehio.pdf","download_url":"https://www.academia.edu/attachments/112619269/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Evaluation_of_Anonymous_and_Expressed_Se.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/112619269/059.036.030620240321-1-fyehio-libre.pdf?1711023008=\u0026response-content-disposition=attachment%3B+filename%3DEvaluation_of_Anonymous_and_Expressed_Se.pdf\u0026Expires=1732776032\u0026Signature=ELBaBOwbI7meAHvi4zrCqjcpEOtqFW1tu8ukJcYDx45ZIahGfDTbCJosjyHwejPNE5LVDUVG8BPc513AMtAa4MidR7boxgeh3TL9FQyHiZX60mk5I8CMPRHNgmCP~-Ij5OxroO1kJlt322Tnp9ziJt8-mXj5ipsHynNq54mYAjWItnf2SWF3PLkTXTkKrcYBwB5obLRYcQ07-7TopbPNfDdq1EF~ZJlm1i0ikRaZ2V7pORSwBBnqhHtoBojykDmoTT-khHeuug86nh9aJAi51rf7SNFel0PYP1gk7tJTfdbqWSFt6K4xKbvWit31qo9lTeP~nyv4ffPDWZm2WyHy8Q__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":173,"name":"Zoology","url":"https://www.academia.edu/Documents/in/Zoology"},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":151887,"name":"Microsatellite","url":"https://www.academia.edu/Documents/in/Microsatellite"},{"id":286323,"name":"Noctuidae","url":"https://www.academia.edu/Documents/in/Noctuidae"},{"id":725411,"name":"Heliothis Virescens","url":"https://www.academia.edu/Documents/in/Heliothis_Virescens"}],"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="116508554"><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/116508554/Short_Communication_Development_and_characterization_of_microsatellite_loci_for_genetic_studies_of_the_sugarcane_borer_Diatraea_saccharalis_Lepidoptera_Crambidae_"><img alt="Research paper thumbnail of Short Communication Development and characterization of microsatellite loci for genetic studies of the sugarcane borer, Diatraea saccharalis (Lepidoptera: Crambidae)" class="work-thumbnail" src="https://attachments.academia-assets.com/112619208/thumbnails/1.jpg" /></a></div><div class="wp-workCard 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class="work-thumbnail" src="https://attachments.academia-assets.com/94003433/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/90440290/Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift">Use of host plants by Troidini butterflies (Papilionidae, Papilioninae): constraints on host shift</a></div><div class="wp-workCard_item"><span>Biological Journal of the Linnean Society</span><span>, 2007</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="86892dc5c094124b9ad2ffa28bff900d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" 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phylogenetic analyses were conducted to determine relationships and to investigate character evolution for the Troidini/ Aristolochia interaction, in an attempt to answer the following questions: (1) what is the present pattern of use of Aristolochia by these butterflies; (2) is the pattern we see today related to the phylogeny of plants or to their chemical composition; (3) can the geographical distribution of Aristolochia explain the host plant use observed today; and (4) how did the interaction between Troidini and Aristolochia evolve? Analyses of character optimization suggest that the current pattern of host plant use of these butterflies does not seem to be constrained by the phylogeny of their food plants, neither by the secondary chemicals in these plants nor by their geographical similarity. The current host plant use in these butterflies seems to be simply opportunistic, with species with a wider geographical range using more species of host plants than those with a more restricted distribution.","publication_date":{"day":null,"month":null,"year":2007,"errors":{}},"publication_name":"Biological Journal of the Linnean Society","grobid_abstract_attachment_id":94003433},"translated_abstract":null,"internal_url":"https://www.academia.edu/90440290/Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift","translated_internal_url":"","created_at":"2022-11-10T03:28:43.005-08:00","preview_url":null,"current_user_can_edit":null,"current_user_is_owner":null,"owner_id":61812500,"coauthors_can_edit":true,"document_type":"paper","co_author_tags":[],"downloadable_attachments":[{"id":94003433,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/94003433/thumbnails/1.jpg","file_name":"j.1095-8312.2007.00727.x.pdf","download_url":"https://www.academia.edu/attachments/94003433/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Use_of_host_plants_by_Troidini_butterfli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/94003433/j.1095-8312.2007.00727.x-libre.pdf?1668095573=\u0026response-content-disposition=attachment%3B+filename%3DUse_of_host_plants_by_Troidini_butterfli.pdf\u0026Expires=1732776032\u0026Signature=U~eizskxLeeNvosQgI0k0EW7bgw1Ufa77xT1egR5KdNLF5eILqYadFKX4oCSGl3~YZbPy9Yj-MZZRNRbphTqQ3Kw2P6egva6vQmMJobkS5pN0ZYQ7yuTJeGij3xnXrLywqojIh-UPSlncLeO2ojONHcTo2iTCSKI~XMxhDhoEuuG~z5Ufb~muwVmR1GKewtOpcrX2oCdlFvXTzYFmusupioJoUCT4GK82Vq01UoS4yD4bigtH1s8d2CTCt~UNdW5bSqCCNrGU47ok1NM~AKyTGM6NzpXqgsEOqSgStUWSx1C~tA8eT7D6xuxSnCcdia2Ns7RbRvNwfFeP5jsAPuxgw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"slug":"Use_of_host_plants_by_Troidini_butterflies_Papilionidae_Papilioninae_constraints_on_host_shift","translated_slug":"","page_count":15,"language":"en","content_type":"Work","owner":{"id":61812500,"first_name":"Karina","middle_initials":null,"last_name":"Silva-brandão","page_name":"KarinaSilvabrandão","domain_name":"independent","created_at":"2017-03-20T13:00:34.821-07:00","display_name":"Karina Silva-brandão","url":"https://independent.academia.edu/KarinaSilvabrand%C3%A3o"},"attachments":[{"id":94003433,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/94003433/thumbnails/1.jpg","file_name":"j.1095-8312.2007.00727.x.pdf","download_url":"https://www.academia.edu/attachments/94003433/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&","bulk_download_file_name":"Use_of_host_plants_by_Troidini_butterfli.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/94003433/j.1095-8312.2007.00727.x-libre.pdf?1668095573=\u0026response-content-disposition=attachment%3B+filename%3DUse_of_host_plants_by_Troidini_butterfli.pdf\u0026Expires=1732776032\u0026Signature=U~eizskxLeeNvosQgI0k0EW7bgw1Ufa77xT1egR5KdNLF5eILqYadFKX4oCSGl3~YZbPy9Yj-MZZRNRbphTqQ3Kw2P6egva6vQmMJobkS5pN0ZYQ7yuTJeGij3xnXrLywqojIh-UPSlncLeO2ojONHcTo2iTCSKI~XMxhDhoEuuG~z5Ufb~muwVmR1GKewtOpcrX2oCdlFvXTzYFmusupioJoUCT4GK82Vq01UoS4yD4bigtH1s8d2CTCt~UNdW5bSqCCNrGU47ok1NM~AKyTGM6NzpXqgsEOqSgStUWSx1C~tA8eT7D6xuxSnCcdia2Ns7RbRvNwfFeP5jsAPuxgw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology"},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences"},{"id":1302079,"name":"Host Plant","url":"https://www.academia.edu/Documents/in/Host_Plant"},{"id":1569877,"name":"Host Shift","url":"https://www.academia.edu/Documents/in/Host_Shift"}],"urls":[]}, dispatcherData: dispatcherData }); 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AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within populations. Clustering analyzes also indicated low genetic differentiation. The haplotype network obtained with combined datasets resulted in 35 haplotypes, with 28 exclusive occurrences, four of them sampled only from soybean fields. The minimum spanning network showed star-shaped structures typical of populations that underwent a recent demographic expansion. The recent expansion was supported by other demographic analyzes, such as the Bayesian skyline plot, the unimodal distribution of paired differences among mitochondr...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6044a4595ee7345addafc520eeac8bac" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":94002110,"asset_id":90438463,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/94002110/download_file?st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&st=MTczMjc3MjQzMiw4LjIyMi4yMDguMTQ2&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="90438463"><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="90438463"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 90438463; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=90438463]").text(description); $(".js-view-count[data-work-id=90438463]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 90438463; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='90438463']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 90438463, 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: "6044a4595ee7345addafc520eeac8bac" } } $('.js-work-strip[data-work-id=90438463]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":90438463,"title":"Genetic variability and demographic history ofHeliothis virescens(Lepidoptera: Noctuidae) populations from Brazil inferred by mtDNA sequences","translated_title":"","metadata":{"abstract":"Intra- and inter-population genetic variability and the demographic history ofHeliothis virescens(F.) populations were evaluated by using mtDNA markers (coxI, coxIIandnad6) with samples from the major cotton- and soybean-producing regions in Brazil in the growing seasons 2007/08, 2008/09 and 2009/10. AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within populations. Clustering analyzes also indicated low genetic differentiation. The haplotype network obtained with combined datasets resulted in 35 haplotypes, with 28 exclusive occurrences, four of them sampled only from soybean fields. The minimum spanning network showed star-shaped structures typical of populations that underwent a recent demographic expansion. The recent expansion was supported by other demographic analyzes, such as the Bayesian skyline plot, the unimodal distribution of paired differences among mitochondr...","publisher":"Cambridge University Press (CUP)","ai_title_tag":"Genetic Variability and Demographic History of Heliothis virescens in Brazil","publication_date":{"day":null,"month":null,"year":2011,"errors":{}},"publication_name":"Bulletin of Entomological Research"},"translated_abstract":"Intra- and inter-population genetic variability and the demographic history ofHeliothis virescens(F.) populations were evaluated by using mtDNA markers (coxI, coxIIandnad6) with samples from the major cotton- and soybean-producing regions in Brazil in the growing seasons 2007/08, 2008/09 and 2009/10. AMOVA indicated low and non-significant genetic structure, regardless of geographical scale, growing season or crop, with most of genetic variation occurring within 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="81448372"><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/81448372/Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations"><img alt="Research paper thumbnail of Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations" 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/81448372/Data_from_Incompatible_ages_for_clearwing_butterflies_based_on_alternative_secondary_calibrations">Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations</a></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.&#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. Our study exemplifies the difficulty of testing hypotheses of divergence times and of choosing between alternative dating scenarios, and shows that age estimates based on seemingly plausible calibrations may be grossly incongruent</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="81448372"><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="81448372"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 81448372; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=81448372]").text(description); $(".js-view-count[data-work-id=81448372]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 81448372; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='81448372']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span><span><script>$(function() { new Works.PaperRankView({ workId: 81448372, 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" } } $('.js-work-strip[data-work-id=81448372]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":81448372,"title":"Data from: Incompatible ages for clearwing butterflies based on alternative secondary calibrations","translated_title":"","metadata":{"abstract":"The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.\u0026#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. Our study exemplifies the difficulty of testing hypotheses of divergence times and of choosing between alternative dating scenarios, and shows that age estimates based on seemingly plausible calibrations may be grossly incongruent","publisher":"Dryad Digital Repository","publication_date":{"day":null,"month":null,"year":2015,"errors":{}}},"translated_abstract":"The recent publication of a time-tree for the plant family Solanaceae (nightshades) provides the opportunity to use independent calibrations to test divergence times previously inferred for the diverse Neotropical butterfly tribe Ithomiini. Ithomiini includes clades that are obligate herbivores of Solanaceae, with some genera feeding on only one genus. We used 8 calibrations extracted from the plant tree in a new relaxed molecular-clock analysis to produce an alternative temporal framework for the diversification of ithomiines. We compared the resulting age estimates to: (i) a time-tree obtained using 7 secondary calibrations from the Nymphalidae tree of Wahlberg et al. (2009), and (ii) Wahlberg et al.\u0026#39;s (2009) original age estimates for the same clades. We found that Bayesian clock estimates were rather sensitive to a variety of analytical parameters, including taxon sampling. Regardless of this sensitivity however, ithomiine divergence times calibrated with the ages of nightshades were always on average half the age of previous estimates. Younger dates for ithomiine clades appear to fit better with factors long suggested to have promoted diversification of the group such as the uplifting of the Andes, in the case of montane genera. Alternatively, if ithomiines are as old as previous estimates suggest, the recent ages inferred for the diversification of Solanaceae seem likely to be seriously underestimated. 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