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We prioritise papers that address the evolutionary process, from a broad perspective. We cover both micro- and macro-evolution of all types of organisms. The aim of the Journal is to integrate perspectives across molecular and microbial evolution, behaviour, genetics, ecology, life histories, development, palaeontology, systematics and morphology. To fulfil its integrative role, the Journal gives preference to papers that bring together two or more fields. The Journal seeks a balance, even a tension, between theory and data. The Editorial Board reflects the multidisciplinary role of the Journal and its international focus. We offer fast-track submission by considering papers from other journals or web outlets, including papers published on pre-print servers, accompanied by previous qualified reviews through ScholarOne or alternative reviewing schemes (such as PCI, Peerage of Science etc.). The manuscript format is of secondary importance initially. Please note: papers that are narrow in scope, and\u002For address an issue from a circumscribed taxonomically-oriented view rather than emphasise general evolutionary issues, are liable to editorial rejection.",{"VOID":19},"14209101",{"EN":21},"Journal of Evolutionary Biology","PUBLISHER","PENDING",null,0,[27],{"id":28,"createTime":29,"updateTime":30,"relativeEntities":31,"label":32,"description":34,"parentId":24,"standard":24,"scholarHubFieldId":24},"d01c5fde-3663-4bb5-9a9e-b5ebea4f38e2","2023-05-29T10:24:13.370+00:00","2023-11-21T07:49:36.907+00:00",[],{"EN":33},"Ecology, Evolution, Behavior and Systematics",{},[36,48],{"id":37,"createTime":38,"updateTime":39,"relativeEntities":40,"slug":41,"properties":42,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":46,"url":24,"parentIds":47,"statistic":24},"05e99a76-c414-4c8f-ae6d-56ed57566774","2023-05-29T10:24:03.197+00:00","2025-11-21T10:07:43.751+00:00",[],"Wiley-Blackwell-Publishing-Ltd",{"title":43},{"EN":44},"Wiley-Blackwell Publishing Ltd","AFFILIATION",5,[],{"id":49,"createTime":50,"updateTime":51,"relativeEntities":52,"slug":53,"properties":54,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":56,"url":24,"parentIds":57,"statistic":24},"43d4a537-d044-4372-8544-ca45c3bea38f","2023-05-29T12:06:07.474+00:00","2024-02-13T10:28:57.921+00:00",[],"WILEY",{"title":55},{"EN":53},6,[],[59,78],{"id":60,"indexDatabase":61,"url":73,"indexYears":74,"academicFieldIds":75,"indexDatabaseRanking":77},"2d530b4e-ddf7-44f0-9ff1-bfc4bfab5f74",{"id":62,"createTime":63,"updateTime":64,"relativeEntities":65,"label":66,"description":68,"key":70,"publicationTags":71,"standard":24},"3c7051d4-eb7d-4c57-a56b-36fc74c5d1e9","2023-05-22T09:57:18.509+00:00","2025-11-21T10:07:52.274+00:00",[],{"EN":67,"VI":67},"Scopus - Elsevier",{"EN":67,"VI":69},"Cơ sở dữ liệu Scopus thuộc Elsevier","scopus",[72],"SCOPUS","https:\u002F\u002Fwww.scopus.com\u002Fsourceid\u002F18920","1988-2025",[76],"95f8925b-50ef-457e-b85f-1ad0343f04b9","SCOPUS__Q1",{"id":79,"indexDatabase":80,"url":94,"indexYears":24,"academicFieldIds":95,"indexDatabaseRanking":24},"01797d39-e84f-4db7-bc9b-4123728fea62",{"id":81,"createTime":82,"updateTime":83,"relativeEntities":84,"label":85,"description":87,"key":90,"publicationTags":91,"standard":24},"a4921856-b128-4d9f-8f1f-e80813d3bbd4","2023-05-22T09:59:31.026+00:00","2025-11-21T10:07:52.153+00:00",[],{"EN":86,"VI":86},"ISI\u002FSCIE - Science Citation Index Expanded",{"VI":88,"EN":89},"Cơ sở dữ liệu SCIE","SCIE database","scie",[92,93],"SCIE","ISI","https:\u002F\u002Fmjl.clarivate.com\u002Fsearch-results?issn=1010-061X",[96,97,98],"7239776a-b6cb-4a11-9a6b-ddd412da67c5","a88c02c1-1408-46e6-b021-2667e298d14d","7b8a31eb-649c-4a9d-9367-0eddb719369e","https:\u002F\u002Fonlinelibrary.wiley.com\u002Fjournal\u002F14209101",{"impactFactor":25,"impactFactorByYear":101,"i10Index":105,"i10IndexLast5Year":25,"totalPublication":105,"totalPublicationByYear":106,"totalCitation":109,"totalCitationByYear":110,"totalCitationPerPublication":120,"totalCitationPerPublicationByYear":121,"hindexLast5Year":105,"hindex":105},{"2012":102,"2013":103,"2014":103,"2015":104,"2018":56},4.5,3,9,10,{"1997":107,"2000":107,"2005":108,"2006":107,"2009":107,"2010":107,"2011":107,"2013":107,"2016":107},1,2,1483,{"1997":111,"2000":112,"2005":113,"2006":114,"2009":115,"2010":116,"2011":117,"2013":118,"2016":119},106,262,826,82,64,31,20,47,45,148.3,{"1997":111,"2000":112,"2005":122,"2006":114,"2009":115,"2010":116,"2011":117,"2013":118,"2016":119},413,{"meta":124,"data":126},{"total":125},"61",[127,257,609,1069,1539,1953,2359,2877,3231,3768],{"id":128,"createTime":129,"updateTime":129,"relativeEntities":130,"slug":131,"properties":132,"entityType":144,"verifyStatus":145,"verifyTime":146,"verifyNote":147,"syncStatus":23,"languages":148,"translateLanguages":24,"viewCount":25,"primaryUrl":150,"fullTextUrl":24,"authors":151,"publicationType":205,"publisherRelationship":206,"citationCount":244,"citationInfo":245,"publishDate":253,"publishYear":254,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":255,"isForceReanalyzing":256},"b5dbe370-60ae-4622-b92a-43797d4a7429","2024-10-12T23:43:29.866+00:00",[],"Evolution-of-colour-patterns-in-East-African-cichlid-fish",{"mag":133,"keywords":135,"openalex":136,"abstract":138,"title":140,"doi":142},{"VOID":134},"1980290756",{},{"VOID":137},"W1980290756",{"EN":139},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>African cichlid fishes have undergone outbursts of explosive speciation in several lakes, accompanied by rapid radiations in coloration and ecology. Little is known about the evolutionary forces that triggered these events but a hypothesis, published by Wallace Dominey in 1984, has figured prominently. It states that the evolution of colour patterns is driven by sexual selection and that these colour patterns are important in interspecific mate choice, a combination which holds the potential for rapid speciation. Here we present phylogenetic analyses that describe major events in colour evolution and test predictions yielded by Dominey's hypothesis. We assembled information on stripe patterns and the presence or absence of nuptial coloration from more than 700 cichlid species representing more than 90 taxa for which molecular phylogenetic hypotheses were available. We show that sexual selection is most likely the selection force that made male nuptial coloration arise and evolve quickly. In contrast, stripe patterns, though phylogenetically not conserved either, are constrained ecologically. The evolution of vertical bar patterns is associated with structurally complex habitats, such as rocky substrates or vegetation. The evolution of a horizontal stripe is associated with a piscivorous feeding mode. Horizontal stripes are also associated with shoaling behaviour. Strength of sexual selection, measured in terms of the mating system (weak in monogamous, strong in promiscuous species), has no detectable effects on stripe pattern evolution. In promiscuous species the frequency of difference between sister species in nuptial hue is higher than in pair bonding and harem forming species, but the frequency of difference in stripe pattern is lower. We argue that differences between the two components of coloration in their exposure to natural selection explain their very different evolutionary behaviour. Finally, we suggest that habitat-mediated selection upon chromomotor flexibility, a special form of phenotypic plasticity found in the river-dwelling outgroups of the lake-dwelling cichlids, explains the rapid and recurrent ecology-associated radiation of stripe patterns in lake environments, a new hypothesis that yields experimentally testable predictions.\u003C\u002Fjats:p>",{"EN":141},"Evolution of colour patterns in East African cichlid fish",{"VOID":143},"10.1046\u002Fj.1420-9101.1999.00055.x","PUBLICATION","VERIFIED","2024-10-12T23:43:29.865+00:00","Auto Verify",[149],"EN","https:\u002F\u002Facademic.oup.com\u002Fjeb\u002Farticle\u002F12\u002F3\u002F514-534\u002F7322952",[152,173,190],{"id":153,"sortIndex":107,"researcher":24,"roles":154,"affiliations":155,"properties":166},"a1910b3e-08b5-4a34-86ff-1a24ca1e561d",[],[156],{"id":157,"sortIndex":25,"affiliation":158,"properties":24},"19e03c6f-12d9-49fa-858a-c8d48c62f2a2",{"id":159,"createTime":160,"updateTime":160,"relativeEntities":161,"slug":162,"properties":163,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"d25710b7-da63-4939-9e57-ae447e547ced","2024-10-12T23:43:29.877+00:00",[],"Institute-of-Evolutionary-and-Ecological-Sciences-University-of-Leiden-PO-Box-9516-NL-2300-RA-Leiden-The-Netherlands-",{"title":164},{"EN":165},"Institute of Evolutionary and Ecological Sciences, University of Leiden, PO Box 9516, NL-2300 RA Leiden, The Netherlands.",{"openalex":167,"orcid":169,"title":171},{"VOID":168},"A5057388085",{"VOID":170},"https:\u002F\u002Forcid.org\u002F0000-0002-7346-6560",{"EN":172},"Peter J. 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Colour differences between allopatric populations of the South American cichlid genus Apistogramma are known for many species, yet the status of such populations has not been previously tested. Analysis of the genetic relationships and mate choice characteristics of populations previously described as Apistogramma caetei from eastern Amazonia indicates genetic differentiation into at least three allopatric lineages, which also show strong prezygotic isolation through female mate choice, confirming them as Biological species. If future studies confirm that this result is indicative of a general trend, the species richness of the South American cichlid fishes may presently be seriously underestimated.\u003C\u002Fjats:p>",{"EN":271},"Colour forms of Amazonian cichlid fish represent reproductively isolated species",{"VOID":273},"16780514",{"VOID":275},"10.1111\u002Fj.1420-9101.2006.01088.x",[149],"https:\u002F\u002Facademic.oup.com\u002Fjeb\u002Farticle\u002F19\u002F4\u002F1139-1148\u002F7324214",[279,300,333,350,367,384],{"id":280,"sortIndex":252,"researcher":24,"roles":281,"affiliations":282,"properties":293},"c21d3ac3-847e-4254-ae35-ba8c2253d698",[],[283],{"id":284,"sortIndex":25,"affiliation":285,"properties":24},"760aaf51-50a1-4b59-8720-4ff003950193",{"id":286,"createTime":287,"updateTime":287,"relativeEntities":288,"slug":289,"properties":290,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"7335cf81-e9e6-4b17-983b-bc5dec19c0ce","2024-10-12T23:43:10.592+00:00",[],"Federal-University-of-the-State-of-Par%C3%A1-Bragan%C3%A7a-PA-Brazil",{"title":291},{"EN":292},"Federal University of the State of Pará, Bragança, PA, Brazil",{"openalex":294,"orcid":296,"title":298},{"VOID":295},"A5081570308",{"VOID":297},"https:\u002F\u002Forcid.org\u002F0000-0003-0982-0227",{"EN":299},"Taciéli dos Santos",{"id":301,"sortIndex":25,"researcher":24,"roles":302,"affiliations":303,"properties":326},"03362e45-4c72-4d22-8718-28e5d90183d0",[],[304,315],{"id":305,"sortIndex":107,"affiliation":306,"properties":24},"bad3d217-1385-4620-b50a-aecc92df44d9",{"id":307,"createTime":308,"updateTime":309,"relativeEntities":310,"slug":311,"properties":312,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"d4fef79a-0791-412f-bf58-60f2cd84178f","2023-11-29T23:41:59.914+00:00","2024-10-12T23:43:10.582+00:00",[],"Department-of-Vertebrate-Zoology-Swedish-Museum-of-Natural-History-Stockholm-Sweden",{"title":313},{"VI":314},"Department of Vertebrate Zoology, Swedish Museum of Natural History, Stockholm, Sweden",{"id":316,"sortIndex":25,"affiliation":317,"properties":24},"a37e1a9d-4834-475e-b3fa-9e60a157edf2",{"id":318,"createTime":319,"updateTime":320,"relativeEntities":321,"slug":322,"properties":323,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"b54eaa53-92af-4643-800a-13020886ab44","2024-04-11T13:48:44.820+00:00","2024-10-12T23:43:10.579+00:00",[],"Department-of-Biological-Sciences-University-of-Hull-Hull-UK",{"title":324},{"EN":325},"Department of Biological Sciences, University of Hull, Hull, UK",{"openalex":327,"orcid":329,"title":331},{"VOID":328},"A5036644834",{"VOID":330},"https:\u002F\u002Forcid.org\u002F0000-0002-9374-8661",{"EN":332},"Jonathan Stuart Ready",{"id":334,"sortIndex":46,"researcher":24,"roles":335,"affiliations":336,"properties":343},"721c79cb-12f9-4ac3-99f8-33d125b24012",[],[337],{"id":338,"sortIndex":25,"affiliation":339,"properties":24},"f8bf5db4-e515-4f0b-8779-b403eef361b6",{"id":318,"createTime":319,"updateTime":320,"relativeEntities":340,"slug":322,"properties":341,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},[],{"title":342},{"EN":325},{"openalex":344,"orcid":346,"title":348},{"VOID":345},"A5034346050",{"VOID":347},"https:\u002F\u002Forcid.org\u002F0000-0003-0099-7261",{"EN":349},"George F. 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USA, 86, 6196, 10.1073\u002Fpnas.86.16.6196",{"doi":501},"10.1073\u002Fpnas.86.16.6196",{"id":24,"text":503,"url":24,"identifiers":504},"Koslowski, 2002, Die Buntbarsche Amerikas Band 2 Apistogramma & Co",{},{"id":24,"text":506,"url":24,"identifiers":507},"Kullander, 1980, A taxonomical study of the genus Apistogramma Regan, with a revision of Brazilian and Peruvian species (Teleostei: Percoidei: Cichlidae), Bonn. Zool. Mono., 14, 1",{},{"id":24,"text":509,"url":24,"identifiers":510},"Kullander, 1991, Review of the South-American Cichlid Genus Mesonauta, Gunther (Teleostei, Cichlidae), with Descriptions of 2 new species, Rev. Suisse De Zool., 98, 407, 10.5962\u002Fbhl.part.79799",{"doi":511},"10.5962\u002Fbhl.part.79799",{"id":24,"text":513,"url":24,"identifiers":514},"Lee, 1995, Structure and evolution of teleost mitochondrial control regions, J. Mol. 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Reihe, 8, 357",{},{"id":24,"text":548,"url":24,"identifiers":549},"Plenderleith, 2005, Female preference for conspecific males based on olfactory cues in a Lake Malawi cichlid fish, Biol. Let., 10.1098\u002Frsbl.2005.0355",{"doi":550},"10.1098\u002Frsbl.2005.0355",{"id":24,"text":552,"url":24,"identifiers":553},"Posada, 1998, Modeltest: testing the model of DNA substitution, Bioinformatics, 14, 817, 10.1093\u002Fbioinformatics\u002F14.9.817",{"doi":554},"10.1093\u002Fbioinformatics\u002F14.9.817",{"id":24,"text":556,"url":24,"identifiers":557},"Posada, 2000, geodis: a program for the cladistic nested analysis of the geographical distribution of genetic haplotypes, Mol. Ecol., 9, 487, 10.1046\u002Fj.1365-294x.2000.00887.x",{"doi":558},"10.1046\u002Fj.1365-294x.2000.00887.x",{"id":24,"text":560,"url":24,"identifiers":561},"Price, 2002, The evolution of F-1 postzygotic incompatibilities in birds, Evolution, 56, 2083",{},{"id":24,"text":563,"url":24,"identifiers":564},"Rambaut, 2001, treeedit: phylogenetic tree editor v. 1.0 alpha 8",{},{"id":24,"text":566,"url":24,"identifiers":567},"Reis, 2003, Check List of the Freshwater Fishes of South and Central America",{},{"id":24,"text":569,"url":24,"identifiers":570},"Richter, 1988, The red form of Apistogramma agassizii, Trop. Fish Hob., 37, 10",{},{"id":24,"text":572,"url":24,"identifiers":573},"Sanderson, 1997, A non-parametric approach to estimating divergence times in the absence of rate constancy, Mol. Biol. 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Südamerikanische Zwergbuntbarsche",{},{"id":24,"text":583,"url":24,"identifiers":584},"Swofford, 1998, paup* Phylogenetic Analysis Using Parsimony (* and other methods)",{},{"id":24,"text":586,"url":24,"identifiers":587},"Templeton, 1995, Separating population structure from population history: a cladistic analysis of the geographical distribution of mitochondrial DNA haplotypes in the tiger salamander, Ambystoma tigrinum, Genetics, 140, 767, 10.1093\u002Fgenetics\u002F140.2.767",{"doi":588},"10.1093\u002Fgenetics\u002F140.2.767",{"id":24,"text":590,"url":24,"identifiers":591},"Templeton, 1998, Nested clade analyses of phylogeographic data: testing hypotheses about gene flow and population history, Mol. Ecol., 7, 381, 10.1046\u002Fj.1365-294x.1998.00308.x",{"doi":592},"10.1046\u002Fj.1365-294x.1998.00308.x",{"id":24,"text":594,"url":24,"identifiers":595},"Templeton, 2001, Using phylogeographic analyses of gene trees to test species status and processes, Mol. Ecol., 10, 779, 10.1046\u002Fj.1365-294x.2001.01199.x",{"doi":596},"10.1046\u002Fj.1365-294x.2001.01199.x",{"id":24,"text":598,"url":24,"identifiers":599},"Tregenza, 2002, Divergence and reproductive isolation in the early stages of speciation, Genetica, 116, 291, 10.1023\u002FA:1021257114996",{"doi":600},"10.1023\u002FA:1021257114996",{"id":24,"text":602,"url":24,"identifiers":603},"Turner, 2001, How many species of cichlid fishes are there in African lakes, Mol. Ecol., 10, 793, 10.1046\u002Fj.1365-294x.2001.01200.x",{"doi":604},"10.1046\u002Fj.1365-294x.2001.01200.x",{"id":24,"text":606,"url":24,"identifiers":607},"Walker, 1991, On the patterns of biomass transfer in the Benthic Fauna of an Amazonian black-water river, as evidenced by P-32 label experiment, Hydrobiologia, 215, 153, 10.1007\u002FBF00014718",{"doi":608},"10.1007\u002FBF00014718",{"id":610,"createTime":611,"updateTime":612,"relativeEntities":613,"slug":614,"properties":615,"entityType":144,"verifyStatus":145,"verifyTime":631,"verifyNote":147,"syncStatus":23,"languages":632,"translateLanguages":24,"viewCount":25,"primaryUrl":633,"fullTextUrl":24,"authors":634,"publicationType":205,"publisherRelationship":680,"citationCount":25,"citationInfo":717,"publishDate":719,"publishYear":720,"citationAnalyzeStatus":721,"lastCitationAnalyze":612,"indexDatabases":24,"openAccess":24,"references":722,"isForceReanalyzing":256},"b38727c3-6526-4562-810d-33ae6d718d51","2025-01-01T03:51:23.989+00:00","2026-05-28T23:41:26.699+00:00",[],"MHC-studies-in-nonmodel-vertebrates-what-have-we-learned-about-natural-selection-in-15-years-",{"mag":616,"keywords":618,"openalex":619,"abstract":621,"title":623,"pm":625,"doi":627,"gsPaper":629},{"VOID":617},"1652383174",{},{"VOID":620},"W1652383174",{"EN":622},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\n               \u003Cjats:p>Elucidating how natural selection promotes local adaptation in interaction with migration, genetic drift and mutation is a central aim of evolutionary biology. While several conceptual and practical limitations are still restraining our ability to study these processes at the DNA level, genes of the major histocompatibility complex (MHC) offer several assets that make them unique candidates for this purpose. Yet, it is unclear what general conclusions can be drawn after 15 years of empirical research that documented MHC diversity in the wild. The general objective of this review is to complement earlier literature syntheses on this topic by focusing on MHC studies other than humans and mice. This review first revealed a strong taxonomic bias, whereby many more studies of MHC diversity in natural populations have dealt with mammals than all other vertebrate classes combined. Secondly, it confirmed that positive selection has a determinant role in shaping patterns of nucleotide diversity in MHC genes in all vertebrates studied. Yet, future tests of positive selection would greatly benefit from making better use of the increasing number of models potentially offering more statistical rigour and higher resolution in detecting the effect and form of selection. Thirdly, studies that compared patterns of MHC diversity within and among natural populations with neutral expectations have reported higher population differentiation at MHC than expected either under neutrality or simple models of balancing selection. Fourthly, several studies showed that MHC-dependent mate preference and kin recognition may provide selective factors maintaining polymorphism in wild outbred populations. However, they also showed that such reproductive mechanisms are complex and context-based. Fifthly, several studies provided evidence that MHC may significantly influence fitness, either by affecting reproductive success or progeny survival to pathogens infections. Overall, the evidence is compelling that the MHC currently represents the best system available in vertebrates to investigate how natural selection can promote local adaptation at the gene level despite the counteracting actions of migration and genetic drift. We conclude this review by proposing several directions where future research is needed.\u003C\u002Fjats:p>",{"EN":624},"MHC studies in nonmodel vertebrates: what have we learned about natural selection in 15 years?",{"VOID":626},"14635837",{"VOID":628},"10.1046\u002Fj.1420-9101.2003.00531.x",{"VOID":630},"[\"10871495215134916547\"]","2025-01-01T03:51:23.988+00:00",[149],"https:\u002F\u002Facademic.oup.com\u002Fjeb\u002Farticle\u002F16\u002F3\u002F363-377\u002F7323364",[635,658],{"id":636,"sortIndex":25,"researcher":24,"roles":637,"affiliations":638,"properties":649},"e3624478-930f-4b34-b715-a5dfc361b245",[],[639],{"id":640,"sortIndex":25,"affiliation":641,"properties":24},"2ce49b2a-f923-4f22-b95c-63859223a605",{"id":642,"createTime":643,"updateTime":643,"relativeEntities":644,"slug":645,"properties":646,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"101f9394-27b8-41b8-b70d-0aedf2490304","2025-01-01T03:51:24.024+00:00",[],"D%C3%A9partement-de-biologie-Universit%C3%A9-Laval-Ste-Foy-Qu%C3%A9bec-Canada",{"title":647},{"EN":648},"Département de biologie, Université Laval, Ste Foy, Québec, Canada",{"openalex":650,"orcid":652,"title":654,"gsAuthor":656},{"VOID":651},"A5001675482",{"VOID":653},"https:\u002F\u002Forcid.org\u002F0000-0002-8085-9709",{"EN":655},"Louis Bernatchez",{"VOID":657},"[\"yA7aaLwAAAAJ\"]",{"id":659,"sortIndex":107,"researcher":24,"roles":660,"affiliations":661,"properties":673},"70f3fb38-42ee-47bd-9b31-535ba7050840",[],[662],{"id":663,"sortIndex":25,"affiliation":664,"properties":24},"1ac5c72f-b543-428b-9f7e-95cc30e9cd42",{"id":665,"createTime":666,"updateTime":667,"relativeEntities":668,"slug":669,"properties":670,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"3a7c021d-bc49-4d20-9899-059f79debdf2","2024-01-04T04:38:23.485+00:00","2025-01-01T03:51:24.123+00:00",[],"Department-of-Organismic-and-Evolutionary-Biology-Harvard-University-Cambridge-MA-USA",{"title":671},{"VI":672},"Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA",{"openalex":674,"orcid":676,"title":678},{"VOID":675},"A5022044396",{"VOID":677},"https:\u002F\u002Forcid.org\u002F0000-0003-3028-6866",{"EN":679},"Christian R. 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Evol., 15, 496, 10.1016\u002FS0169-5347(00)01994-7",{"doi":1068},"10.1016\u002FS0169-5347(00)01994-7",{"id":1070,"createTime":1071,"updateTime":1071,"relativeEntities":1072,"slug":1073,"properties":1074,"entityType":144,"verifyStatus":145,"verifyTime":1088,"verifyNote":147,"syncStatus":23,"languages":1089,"translateLanguages":24,"viewCount":25,"primaryUrl":1090,"fullTextUrl":24,"authors":1091,"publicationType":205,"publisherRelationship":1113,"citationCount":1150,"citationInfo":1151,"publishDate":1159,"publishYear":1160,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":1161,"isForceReanalyzing":256},"dbb1387f-cd57-412b-99c8-2307a6dad434","2024-10-04T23:15:52.850+00:00",[],"Bursts-of-transposable-elements-as-an-evolutionary-driving-force",{"mag":1075,"keywords":1077,"openalex":1078,"abstract":1080,"title":1082,"pm":1084,"doi":1086},{"VOID":1076},"2052233237",{},{"VOID":1079},"W2052233237",{"EN":1081},"\u003Cjats:title>Abstract\u003C\u002Fjats:title>\u003Cjats:p>A burst of transposable elements (\u003Cjats:styled-content style=\"fixed-case\">TE\u003C\u002Fjats:styled-content>s) is a massive outbreak that may cause radical genomic rebuilding. This phenomenon has been reported in connection with the formation of taxonomic groups and species and has therefore been associated with major evolutionary events in the past. Over the past few years, several research groups have discovered recent stress‐induced bursts of different\u003Cjats:styled-content style=\"fixed-case\">TE\u003C\u002Fjats:styled-content>s. The events for which bursts of\u003Cjats:styled-content style=\"fixed-case\">TE\u003C\u002Fjats:styled-content>s have been recorded include domestication, polyploidy, changes in mating systems, interspecific and intergeneric hybridization and abiotic stress. Cases involving abiotic stress, particularly bursts of\u003Cjats:styled-content style=\"fixed-case\">TE\u003C\u002Fjats:styled-content>s in natural populations driven by environmental change, are of special interest because this phenomenon may underlie micro‐ and macro‐evolutionary events and ultimately support the maintenance and generation of biological diversity. This study reviews the known cases of bursts of\u003Cjats:styled-content style=\"fixed-case\">TE\u003C\u002Fjats:styled-content>s and their possible consequences, with particular emphasis on the speciation process.\u003C\u002Fjats:p>",{"EN":1083},"Bursts of transposable elements as an evolutionary driving 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The present paper examines the evidence for such a trade-off as indicated by genetic correlations between traits. The genetic covariances between traits are derived using a model in which maturation occurs when the organism achieves a genetically variable size threshold, and fecundity is an allometric function of body size with one genetically variable parameter (excluding body size itself). This model predicts that the heritabilities of the life history traits (growth rate, development time, fecundity) will not necessarily be less than the heritability of adult size (i.e. morphological traits). It is shown that if growth rate is genetically correlated with adult size then it is not possible, in general, to predict the sign of the genetic correlation between development time and fecundity. For particular cases the signs of the covariances between traits can be predicted. These predictions are tested using data drawn from the literature.\u003C\u002Fjats:p>",{"EN":1553},"Trade-offs between growth and reproduction: an analysis of the quantitative genetic evidence",{"VOID":1555},"10.1046\u002Fj.1420-9101.2000.00186.x",[149],"https:\u002F\u002Facademic.oup.com\u002Fjeb\u002Farticle\u002F13\u002F3\u002F434-445\u002F7323045",[1559],{"id":1560,"sortIndex":25,"researcher":24,"roles":1561,"affiliations":1562,"properties":1574},"d7942ec2-dcb7-4b15-bfc9-865d2f460e18",[],[1563],{"id":1564,"sortIndex":25,"affiliation":1565,"properties":24},"cb088fe1-dbde-4fa9-87f8-924246418d29",{"id":1566,"createTime":1567,"updateTime":1568,"relativeEntities":1569,"slug":1570,"properties":1571,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"85d9205b-8799-492d-9635-dae2f8f0dae7","2023-12-20T04:13:44.600+00:00","2024-10-06T23:48:28.803+00:00",[],"Department-of-Biology-McGill-University-Montreal-Quebec-Canada",{"title":1572},{"VI":1573},"Department of Biology, McGill University, Montreal, Quebec, Canada",{"openalex":1575,"title":1577},{"VOID":1576},"A5031225420",{"EN":1578},"Roff",{"url":24,"publisher":1580,"properties":1610},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1581,"slug":10,"properties":1582,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":1588,"manageAffiliations":1589,"indexDatabases":1590,"url":99,"thumbnailPath":24,"statistic":1605,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":1583,"issn":1584,"introduce":1585,"eissn":1586,"title":1587},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[1591,1598],{"id":79,"indexDatabase":1592,"url":94,"indexYears":24,"academicFieldIds":1597,"indexDatabaseRanking":24},{"id":81,"createTime":82,"updateTime":83,"relativeEntities":1593,"label":1594,"description":1595,"key":90,"publicationTags":1596,"standard":24},[],{"EN":86,"VI":86},{"VI":88,"EN":89},[92,93],[96,97,98],{"id":60,"indexDatabase":1599,"url":73,"indexYears":74,"academicFieldIds":1604,"indexDatabaseRanking":77},{"id":62,"createTime":63,"updateTime":64,"relativeEntities":1600,"label":1601,"description":1602,"key":70,"publicationTags":1603,"standard":24},[],{"EN":67,"VI":67},{"EN":67,"VI":69},[72],[76],{"impactFactor":25,"impactFactorByYear":1606,"i10Index":105,"i10IndexLast5Year":25,"totalPublication":105,"totalPublicationByYear":1607,"totalCitation":109,"totalCitationByYear":1608,"totalCitationPerPublication":120,"totalCitationPerPublicationByYear":1609,"hindexLast5Year":105,"hindex":105},{"2012":102,"2013":103,"2014":103,"2015":104,"2018":56},{"1997":107,"2000":107,"2005":108,"2006":107,"2009":107,"2010":107,"2011":107,"2013":107,"2016":107},{"1997":111,"2000":112,"2005":113,"2006":114,"2009":115,"2010":116,"2011":117,"2013":118,"2016":119},{"1997":111,"2000":112,"2005":122,"2006":114,"2009":115,"2010":116,"2011":117,"2013":118,"2016":119},{"volume":1611,"pages":1613,"issue":1615},{"VOID":1612},"13",{"VOID":1614},"434-445",{"VOID":243},{"total":112,"publishYear":24,"statisticByYear":1617},{"2012":105,"2013":248,"2014":251,"2015":1618,"2016":56,"2017":249,"2018":1618,"2019":1619,"2020":1153,"2021":251,"2022":249,"2023":108,"2024":105},16,13,"2000-05-01",2000,[1623,1627,1631,1635,1639,1643,1647,1651,1655,1659,1663,1666,1669,1672,1676,1680,1683,1687,1691,1695,1698,1701,1705,1709,1713,1717,1720,1723,1727,1731,1735,1739,1743,1747,1751,1755,1759,1762,1765,1769,1773,1777,1781,1785,1789,1793,1797,1800,1804,1807,1811,1815,1819,1823,1827,1831,1834,1838,1842,1845,1848,1852,1856,1860,1864,1868,1872,1876,1880,1883,1887,1891,1895,1899,1903,1907,1911,1915,1919,1923,1927,1931,1934,1938,1941,1945,1949],{"id":24,"text":1624,"url":24,"identifiers":1625},"Abrams, 1996, The effect of flexible growth rates on optimal sizes and development in a seasonal environment, Am. 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Yet, many other mammals use their forelimbs to grasp and manipulate objects. Previous investigations have suggested that grasping may be derived from digging behaviour, arboreal locomotion or hunting behaviour. Here, we test the arboreal origin of grasping and investigate whether an arboreal lifestyle could confer a greater grasping ability in musteloid carnivorans. Moreover, we investigate the morphological adaptations related to grasping and the differences between arboreal species with different grasping abilities. We predict that if grasping is derived from an arboreal lifestyle, then the anatomical specializations of the forelimb for arboreality must be similar to those involved in grasping. We further predict that arboreal species with a well‐developed manipulation ability will have articulations that facilitate radio‐ulnar rotation. We use ancestral character state reconstructions of lifestyle and grasping ability to understand the evolution of both traits. Finally, we use a surface sliding semi‐landmark approach capable of quantifying the articulations in their full complexity. Our results largely confirm our predictions, demonstrating that musteloids with greater grasping skills differ markedly from others in the shape of their forelimb bones. These analyses further suggest that the evolution of an arboreal lifestyle likely preceded the development of enhanced grasping ability.\u003C\u002Fjats:p>",{"EN":1967},"Getting a grip on the evolution of grasping in musteloid carnivorans: a three‐dimensional analysis of forelimb 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