{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T02:27:17Z","timestamp":1786588037962,"version":"build-2736575974"},"reference-count":64,"publisher":"Wiley","issue":"15","license":[{"start":{"date-parts":[[2026,8,5]],"date-time":"2026-08-05T00:00:00Z","timestamp":1785888000000},"content-version":"vor","delay-in-days":4,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,8,1]],"date-time":"2026-08-01T00:00:00Z","timestamp":1785542400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Molecular Ecology"],"published-print":{"date-parts":[[2026,8]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    The analysis of the genomic architecture of selection can be insightful for the understanding of sexual conflict and sexual selection acting in wild populations. In general, there will be a wide range of possible targets of selection in the reproductive system of sexually promiscuous species. In the context of a dynamic conflict, selection is expected to be predominantly recurrent and it might be best investigated by combining population\u2010level and phylogenetic approaches on multiple species. First, we used population\u2010based methods to scan for recent selection in the socially polygynous pectoral sandpiper (\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>Calidris melanotos<\/jats:italic>\n                    <\/jats:styled-content>\n                    ). We assembled and annotated the pectoral sandpiper genome and re\u2010sequenced the genome of 20 random individuals of a single breeding population. We identified genes coding for axonemal constituents which are mostly expressed in the testis as selection targets. These genes most likely influence energy\u2010driven sperm motility, suggesting a role in sperm competition in this species. Second, we replicated the analysis and found similar results in another promiscuous shorebird, the ruff (\n                    <jats:italic>Calidris pugnax<\/jats:italic>\n                    ), using publicly available data of 25 re\u2010sequenced individuals. Finally, a comparative genomics approach among six\n                    <jats:italic>Calidris<\/jats:italic>\n                    species with publicly available genome assemblies showed similar signals of selection, suggesting historical episodes of postcopulatory sexual selection or sexual conflict in genes related to sperm motility.\n                  <\/jats:p>","DOI":"10.1111\/mec.70493","type":"journal-article","created":{"date-parts":[[2026,8,5]],"date-time":"2026-08-05T07:48:32Z","timestamp":1785916112000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genes Related to Sperm Motility Are Under Recent Ongoing Selection in Two Shorebird Species With a Polygynous Mating System and Frequent Multiple Paternity"],"prefix":"10.1111","volume":"35","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6676-7595","authenticated-orcid":false,"given":"Jakob C.","family":"Mueller","sequence":"first","affiliation":[{"name":"Department of Ornithology Max Planck Institute for Biological Intelligence  Seewiesen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7505-5458","authenticated-orcid":false,"given":"Bart","family":"Kempenaers","sequence":"additional","affiliation":[{"name":"Department of Ornithology Max Planck Institute for Biological Intelligence  Seewiesen Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,8,5]]},"reference":[{"key":"e_1_2_11_2_1","doi-asserted-by":"publisher","DOI":"10.1098\/rstb.2020.0208"},{"key":"e_1_2_11_3_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1005877"},{"key":"e_1_2_11_4_1","doi-asserted-by":"publisher","DOI":"10.1093\/condor\/109.1.1"},{"key":"e_1_2_11_5_1","doi-asserted-by":"publisher","DOI":"10.3389\/fevo.2024.1476254"},{"key":"e_1_2_11_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/humupd\/dmy017"},{"key":"e_1_2_11_7_1","doi-asserted-by":"publisher","DOI":"10.1146\/annurev-genet-111523-102651"},{"key":"e_1_2_11_8_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1000570"},{"key":"e_1_2_11_9_1","doi-asserted-by":"publisher","DOI":"10.1101\/685321"},{"key":"e_1_2_11_10_1","doi-asserted-by":"publisher","DOI":"10.1093\/gbe\/evx131"},{"key":"e_1_2_11_11_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1003905"},{"key":"e_1_2_11_12_1","doi-asserted-by":"publisher","DOI":"10.1038\/nrg2146"},{"key":"e_1_2_11_13_1","doi-asserted-by":"publisher","DOI":"10.1074\/mcp.M113.035600"},{"key":"e_1_2_11_14_1","doi-asserted-by":"publisher","DOI":"10.2173\/bow.pecsan.01"},{"key":"e_1_2_11_15_1","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.0809990106"},{"key":"e_1_2_11_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.cub.2004.05.010"},{"key":"e_1_2_11_17_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pbio.3002469"},{"key":"e_1_2_11_18_1","unstructured":"Garrison E. andG.Marth.2012.Haplotype\u2010Based Variant Detection From Short\u2010Read Sequencing. arXiv preprint arXiv:1207.3907 [q\u2010bio.GN]."},{"key":"e_1_2_11_19_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.isci.2024.110366"},{"key":"e_1_2_11_20_1","doi-asserted-by":"publisher","DOI":"10.1111\/andr.13431"},{"key":"e_1_2_11_21_1","unstructured":"Grote S.2018.GOfuncR: Gene ontology enrichment using FUNC. 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