{"id":1245,"date":"2025-11-07T14:45:05","date_gmt":"2025-11-07T14:45:05","guid":{"rendered":"https:\/\/www.birds.cornell.edu\/clementschecklist\/?page_id=1245"},"modified":"2025-11-07T16:56:50","modified_gmt":"2025-11-07T16:56:50","slug":"updates-and-corrections-october-2025","status":"publish","type":"page","link":"https:\/\/www.birds.cornell.edu\/clementschecklist\/updates-and-corrections-october-2025\/","title":{"rendered":"Updates and Corrections\u2014October 2025"},"content":{"rendered":"\n<p>This document accompanies the <a href=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/introduction\/updateindex\/october-2025\/2025-citation-checklist-downloads\/\" data-type=\"page\" data-id=\"1067\">eBird\/Clements Checklist v2025 spreadsheet<\/a> (tap or click link for downloads and recommended citation).<\/p>\n\n\n\n<p>Note the following:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Numbers preceding accounts are taxon order numbers specific to the 2025 eBird\/Clements update. These differ from year to year but are used here to facilitate sequential treatment.<\/li>\n\n\n\n<li>WGAC (Working Group Avian Checklists of the IOU) is now referred to throughout as AviList. Nearly all decisions taken by AviList (AviList Core Team 2025) have been enacted in Clements et al. (2025).<\/li>\n\n\n\n<li>The IOC-WBL, also known simply as <a href=\"https:\/\/www.worldbirdnames.org\/new\/\">the IOC list<\/a>, is the Gill and Donsker and Gill et al. checklists; the version referred to is always 15.1 unless specifically stated (but note that specific taxonomic decisions may have been implemented in earlier versions than 15.1).<\/li>\n\n\n\n<li>HBW and BirdLife International (2025). <a href=\"https:\/\/datazone.birdlife.org\/about-our-science\/taxonomy#birdlife-s-taxonomic-checklist\">Handbook of the Birds of the World and BirdLife International digital checklist of the birds of the world<\/a>. Version 10.<\/li>\n\n\n\n<li><a href=\"https:\/\/checklist.americanornithology.org\/\">NACC checklist<\/a> <\/li>\n\n\n\n<li><a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCBaseline.htm\">SACC checklist<\/a> <\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Species Gains and Losses<\/h2>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"splits\">Splits<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Red Grouse<\/strong><strong><em> Lagopus scotica<\/em><\/strong><strong> <\/strong>is split from <strong>Willow Ptarmigan <\/strong><strong><em>Lagopus lagopus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The Red Grouse, endemic to the British Isles, differs from all other taxa of Willow Ptarmigan in its molts and plumages, and forms a distinct genetic group.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 1351\u20131372<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Willow Ptarmigan<em> Lagopus lagopus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>variegata<\/em>,<em> lagopus<\/em>, <em>rossica<\/em>, <em>birulai<\/em>, <em>koreni<\/em>, <em>kamtschatkensis<\/em>, <em>maior<\/em>, <em>brevirostris<\/em>, <em>kozlowae<\/em>, <em>sserebrowsky<\/em>, <em>okadai<\/em>, <em>muriei<\/em>, <em>alexandrae<\/em>, <em>alascensis<\/em>, <em>leucoptera<\/em>, <em>alba<\/em>, <em>ungavus<\/em>, <em>alleni, hibernica<\/em>,<em> <\/em>and<em> scotica<\/em>&nbsp;<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Red Grouse<em> Lagopus scotica<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>hibernica <\/em>and<em> scotica<\/em><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Willow Ptarmigan<em> Lagopus lagopus<\/em>&nbsp;<\/li>\n<\/ul>\n\n\n\n<p>subspecies: <em>variegata<\/em>,<em> lagopus<\/em>, <em>rossica<\/em>, <em>birulai<\/em>, <em>koreni<\/em>, <em>kamtschatkensis<\/em>, <em>maior<\/em>, <em>brevirostris<\/em>, <em>kozlowae<\/em>, <em>sserebrowsky<\/em>, <em>okadai<\/em>, <em>muriei<\/em>, <em>alexandrae<\/em>, <em>alascensis<\/em>, <em>leucoptera<\/em>, <em>alba<\/em>, <em>ungavus<\/em>, and <em>alleni<\/em><\/p>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1200\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/1-Lagopus-scotica-graphical-abstract.png\" alt=\"\" class=\"wp-image-1078 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/1-Lagopus-scotica-graphical-abstract.png 1200w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/1-Lagopus-scotica-graphical-abstract-720x432.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/1-Lagopus-scotica-graphical-abstract-768x461.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/1-Lagopus-scotica-graphical-abstract-480x288.png 480w\" data-sizes=\"(max-width: 1200px) 100vw, 1200px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1200px; --smush-placeholder-aspect-ratio: 1200\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the Northern Hemisphere showing the approximate ranges  of the Willow Ptarmigan <em>Lagopus lagopus<\/em> and the Red Grouse <em>Lagopus scotica<\/em>.<\/figcaption><\/figure>\n\n\n\n<p>Long treated as members of the highly polytypic Holarctic Willow Ptarmigan <em>Lagopus lagopus<\/em> (Linnaeus, 1758), the two (or one, depending on taxonomy adopted) taxa in the British Isles, <em>scotica<\/em> (Latham, 1787) and <em>hibernica <\/em>(Kleinschmidt, 1919), are the only ones with wholly dark wings and no molt into a white winter plumage.&nbsp; Despite their very wide distribution, including on islands, all the other subspecies are fairly similar in plumage and molts. In fact, even Peters (1934) treated <em>scotica <\/em>and <em>hibernica <\/em>as separate species. While these morphological aspects were long argued to be of only subspecific importance (as treated by e.g. Wolters 1976), genomic data show that <em>scotica <\/em>and <em>hibernica <\/em>form a monophyletic, fairly well-diverged clade (Quintela et al. 2010, Kozma et al. 2019, Sangster et al. 2022). Nevertheless, they appear to be similar vocally to taxa of <em>Lagopus lagopus<\/em>, although a vocal analysis should be carried out. On balance, the evidence is deemed by AviList Core Team (2025) and NACC (Chesser 2025, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/02\/2025-B.pdf\">2025-B-10<\/a>; Chesser et al. 2025) to support specific status for <em>Lagopus scotica<\/em>, while the recognition of subspecies <em>hibernica <\/em>requires further study, as it is currently recognized by eBird\/Clements (v2025) but not by AviList Core Team (2025).<\/p>\n\n\n\n<p><strong>English names:<\/strong> The English name Red Grouse has been very widely used and is thus deeply entrenched, and thus no change is made in that respect. The Willow Ptarmigan <em>sensu stricto<\/em> has a Holarctic distribution, so its much larger range and the wide familiarity of the English name means that no change is required.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Mexican Squirrel-Cuckoo <\/strong><strong><em>Piaya mexicana<\/em><\/strong><strong> <\/strong>is<strong> <\/strong>split from<strong> Squirrel Cuckoo <\/strong><strong><em>Piaya cayana<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Western Mexico gains another endemic species with the split of the Mexican Squirrel-Cuckoo, which differs somewhat both in vocalizations and plumage from Common Squirrel-Cuckoo.&nbsp;<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 3217\u20133232<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Squirrel Cuckoo <em>Piaya cayana<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>mexicana<\/em>, <em>thermophila, nigricrissa, mehleri, mesura, circe, cayana, insulana, obscura, hellmayri, pallescens, cabanisi, macroura<\/em>, and <em>mogenseni<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Mexican Squirrel-Cuckoo <em>Piaya mexicana <\/em>(monotypic)<\/li>\n\n\n\n<li>Common Squirrel-Cuckoo <em>Piaya cayana<\/em><\/li>\n<\/ul>\n\n\n\n<p>Subspecies: <em>thermophila, nigricrissa, mehleri, mesura, circe, cayana, insulana, obscura, hellmayri, pallescens, cabanisi, macroura<\/em>, and <em>mogenseni<\/em><\/p>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/2-Piaya-mexicana-graphical-abstract.png\" alt=\"\" class=\"wp-image-1079 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/2-Piaya-mexicana-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/2-Piaya-mexicana-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/2-Piaya-mexicana-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/2-Piaya-mexicana-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the Neotropics showing the ranges of the Mexican Squirrel-Cuckoo <em>Piaya mexicana<\/em> and the Common Squirrel-Cuckoo <em>Piaya cayana<\/em>.<\/figcaption><\/figure>\n\n\n\n<p>The West Mexican squirrel cuckoo taxon <em>mexicana <\/em>(Swainson, 1827) was long treated as a subspecies of the widespread, polytypic Neotropical <em>Piaya cayana<\/em> (Linnaeus, 1766), including by Peters (1940) and Wolters (1976), but it was split based on morphological differences by del Hoyo and Collar (2014). A recent study (S\u00e1nchez-Gonz\u00e1lez et al. 2023) showed limited evidence of introgression in a region of parapatry between <em>mexicana <\/em>and <em>thermophila <\/em>Sclater, 1860 in southeastern Mexico, and that <em>mexicana <\/em>forms a monophyletic clade, although it is less deeply diverged from the Middle and northern South American taxa than is the Amazonian <em>cayana <\/em>clade (Smith et al. 2014). However, several vocal differences exist between <em>mexicana <\/em>and all other taxa (Dyer and Howell 2023, Johnson et al. 2025, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/05\/2025-C.pdf\">2025-C-14a,b<\/a>), while the other taxa seem to be more similar to each other vocally.&nbsp;<\/p>\n\n\n\n<p>There is a nomenclatural issue regarding whether the name <em>circe <\/em>Bonaparte, 1850 or <em>mehleri <\/em>Bonaparte, 1850 has priority for the Middle and northern South American taxa. Pending resolution of this issue, AviList Core Team (2025) and Chesser et al. (2025) voted to split only <em>mexicana <\/em>from the remainder at this time. The taxa with greenish eye-rings (<em>thermophila, nigricrissa, circe<\/em>, and <em>insulana<\/em>) of Middle and northern South America should probably be united in one group, while the remaining taxa, which have red eye-rings and occur in Amazonia and southward, should likely be separated in the <em>cayana <\/em>group. Based on apparent parapatry and genetics (Johnson et al. 2025), these are likely to be considered separate species in the future.&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> The English name Mexican Squirrel-Cuckoo has been adopted for the newly split <em>mexicana<\/em>, with Common Squirrel-Cuckoo for <em>Piaya cayana s.s. (<\/em>as used by del Hoyo and Collar 2014 and Chesser et al. 2025). The usage of hyphens denotes that these are considered to form a monophyletic group.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Hudsonian Whimbrel <\/strong><strong><em>Numenius hudsonicus <\/em><\/strong>and<strong> Eurasian Whimbrel <\/strong><strong><em>Numenius phaeopus<\/em><\/strong> are split from <strong>Whimbrel <\/strong><strong><em>Numenius phaeopus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The Hudsonian and Eurasian whimbrels, the former breeding patchily in Nearctic tundra and the latter patchily in Palearctic tundra and steppe, have similar vocalizations but differ strongly in rump color and are deeply diverged genetically.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 6011\u20136017<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Whimbrel <em>Numenius phaeopus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>phaeopus, alboaxillaris, rogachevae<\/em>, <em>variegatus<\/em>, and <em>hudsonicus<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Eurasian Whimbrel <em>Numenius phaeopus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>phaeopus, alboaxillaris, rogachevae<\/em>, and <em>variegatus<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Hudsonian Whimbrel <em>Numenius hudsonicus<\/em><strong> <\/strong>(monotypic)<\/p>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/3-Numenius-hudsonicus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1080 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/3-Numenius-hudsonicus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/3-Numenius-hudsonicus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/3-Numenius-hudsonicus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/3-Numenius-hudsonicus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the world showing the approximate breeding ranges of the two species into which Whimbrel <em>Numenius phaeopus<\/em> has been partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Since about 1934 (Peters 1934), the North American-breeding taxon <em>hudsonicus <\/em>Latham, 1790 of whimbrel has been considered a subspecies of a circumpolar Whimbrel <em>Numenius phaeopus<\/em> (Linnaeus, 1758). This treatment was adopted by the AOS in 1944 (AOS 1944), and subsequently most authorities have considered them conspecific. The most obvious phenotypic difference between <em>hudsonicus <\/em>and the Old World taxa comprising <em>phaeopus <\/em>is the dark rump of the former vs. the white rump of the latter, which has generally been considered an insufficient basis to justify species status. Indeed, one subspecies of Old World <em>phaeopus<\/em>, the steppe-breeding <em>alboaxillaris <\/em>Lowe, 1921 is arguably equally distinct to <em>hudsonicus <\/em>phenotypically, with its white underwing linings, vs. these being heavily barred in other taxa including <em>hudsonicus<\/em>. In addition, vocalizations of all appear similar, unlike those of most other shorebird species pairs, although a formal vocal analysis may show some differences.<\/p>\n\n\n\n<p>However, mtDNA and genomic data (Zink et al. 1995, Humphries and Winker 2011, Tan et al. 2019, McLaughlin et al. 2020) have shown that <em>hudsonicus <\/em>is deeply diverged relative to the Old World taxa, and thus has evidently been reproductively isolated from them for a considerable period. Although their breeding grounds are far apart, these are very long-distance migrants and both the eastern <em>variegatus<\/em>\/<em>rogachevae <\/em>group of <em>phaeopus <\/em>and <em>hudsonicus <\/em>regularly appear in western Alaska (Gibson and Withrow 2015). Although a fairly recent proposal to NACC (Winker 2022, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2022\/04\/2022-A-final.pdf\">2022-A-10<\/a>) did not pass, the deep divergence and evidence for reproductive isolation led AviList Core Team (2025) to consider <em>hudsonicus <\/em>a separate species.&nbsp;<\/p>\n\n\n\n<p><strong>English names: <\/strong>The English names Hudsonian Whimbrel for <em>Numenius hudsonicus <\/em>and Eurasian Whimbrel for <em>Numenius phaeopus <\/em>have previously been widely adopted for this species pair (summarized in Winker 2022), and are therefore used here.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Atlantic White-Tern <em>Gygis alba<\/em>, Blue-billed White-Tern <em>Gygis candida<\/em>, <\/strong>and<strong> Little White-Tern <em>Gygis microrhyncha<\/em> <\/strong>are<strong> <\/strong>split from <strong>White Tern <em>Gygis alba<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21923 species) The beautiful white-terns of tropical seas differ from each other in bill shape and color, and in size, among other ways, and now are treated as three distinct species, one in the Atlantic, one in the Indian and Pacific oceans, and one now only in the Marquesas of the tropical Pacific.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 6626\u20136630<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>White Tern<em> Gygis alba<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>alba, candida, leucopes, and microrhyncha<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Atlantic White-Tern<em> Gygis alba <\/em>(monotypic)<\/li>\n\n\n\n<li>Blue-billed White-Tern<em> Gygis candida&nbsp;<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>candida<\/em> and <em>leucopes<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Little White-Tern<em> Gygis microrhyncha <\/em>(monotypic)<\/p>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/4-Gygis-alba-graphical-abstract.png\" alt=\"\" class=\"wp-image-1081 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/4-Gygis-alba-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/4-Gygis-alba-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/4-Gygis-alba-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/4-Gygis-alba-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of tropical oceans showing the approximate ranges of the three species into which the White Tern <em>Gygis alba<\/em> has been partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Although each was originally described as a full species, <em>Gygis alba<\/em> (Sparrman, 1786) of the tropical Atlantic, <em>candida <\/em>(Gmelin, 1789) (including <em>leucopes <\/em>Holyoak &amp; Thibault, 1976) of the tropical Indo-Pacific, and <em>microrhyncha <\/em>Saunders, 1876 of the eastern tropical Pacific have long been considered conspecific, including by Peters (1934). However, their differences in morphology defy application of criteria typical of subspecies, especially their bill morphology and coloration, but also size and differences in wing and tail shape (Olson 2005, Pratt 2020). Furthermore, there are evidently vocal differences (Pratt 2020), and prehistoric sympatry between <em>candida <\/em>and <em>microrhyncha <\/em>over a wide area (Steadman 2006). However, the range of <em>microrhyncha <\/em>has now contracted markedly, and it apparently hybridizes with <em>candida <\/em>in part of its now-limited range (Pratt 2020). In addition, mtDNA data show only limited genetic divergence, which may be due to introgression (Yeung et al. 2009, Thibault and Cibois 2017).&nbsp;<\/p>\n\n\n\n<p>Based mainly on the marked morphological differences and past sympatry (Pratt 2025a, b), a three-way split was agreed upon by AviList Core Team (2025), NACC (Pratt 2024, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/02\/2025-A.pdf\">2025-A-3a, b<\/a>; Chesser et al. 2025), and <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1045.htm\">SACC<\/a> (Remsen et al. 2025).<\/p>\n\n\n\n<p><strong>English names:<\/strong> We follow the English names adopted by AviList Core Team (2025), NACC (<a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/05\/2025-D.pdf\">2025-D-1<\/a>; Chesser et al. 2025), and SACC: Atlantic White-Tern <em>Gygis alba<\/em>; Blue-billed White-Tern <em>Gygis candida<\/em>; and Little White-Tern <em>Gygis microrhyncha<\/em>. Suggestions that involve some version of \u201cFairy\u201d in the group name were not adopted due to the potential for confusion with <em>Sternula nereis<\/em>, which throughout much of its range (Australia to New Caledonia) has long been known as \u201cFairy Tern\u201d, although in eBird\/Clements (v2025 and prior versions) and AviList Core Team (2025) the name \u201cAustralian Fairy Tern\u201d is used. The group name \u201cWhite Tern\u201d has long usage and is adequate, and is here hyphenated to indicate that it forms a monophyletic group.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Western Rockhopper Penguin<\/strong><strong><em> Eudyptes chrysocome<\/em><\/strong><em> <\/em>and <strong>Eastern Rockhopper Penguin<\/strong><strong><em> Eudyptes filholi<\/em><\/strong> are split from <strong>Southern Rockhopper Penguin<\/strong><strong><em> Eudyptes chrysocome<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The rockhopper penguins of the southern South American region differ from those of southern Indian and southwestern Pacific ocean islands in DNA, and subtly in morphology.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 6965\u20136966<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Southern Rockhopper Penguin<em> Eudyptes chrysocome<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>chrysocome <\/em>and <em>filholi<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Western Rockhopper Penguin<em> Eudyptes chrysocome&nbsp;<\/em><\/li>\n\n\n\n<li>Eastern Rockhopper Penguin<em> Eudyptes filholi<\/em>&nbsp;<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/5-Eudyptes-filholi-graphical-abstract.png\" alt=\"\" class=\"wp-image-1082 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/5-Eudyptes-filholi-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/5-Eudyptes-filholi-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/5-Eudyptes-filholi-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/5-Eudyptes-filholi-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the subantarctic showing the approximate ranges of the two species into which the Southern Rockhopper Penguin <em>Eudyptes chrysocome<\/em> has been partitioned. <\/figcaption><\/figure>\n\n\n\n<p>The subantarctic rockhopper penguins were long considered a single species, <em>Eudyptes chrysocome <\/em>(Forster, 1781), as in Peters (1931) and Wolters (1975). Since then, the populations breeding on temperate-latitude islands in the South Atlantic and South Indian oceans, <em>moseleyi <\/em>Mathews &amp; Iredale, 1921, despite its relatively late description and despite having considered a synonym by some (including Peters 1931 and Wolters 1975), have been shown to be highly distinct in numerous ways, including morphology, genetics, vocalizations, and breeding phenology, and this split has been broadly accepted. The taxonomic status of the southern-breeding populations, however, has been more controversial. It has long been known that the populations breeding in the southern South American region, <em>chrysocome<\/em>, differ from those breeding in the South Indian and Southwest Pacific oceans, <em>filholi <\/em>Hutton, 1879 in morphology, mainly the absence in the former and presence in the latter of a prominent pale pink border to the lower mandible and the gape, as well as a narrower bill, slightly different underwing markings, and typically a narrower yellow stripe above the eye, and indeed <em>filholi <\/em>and <em>chrysocome <\/em>were originally described as separate species. The bill border feature is remarkably consistent within populations, despite the major range disjunction between breeding colonies of <em>filholi <\/em>in the South Indian and Southwest Pacific oceans, and the lack of differentiation between the two latter highly disjunct populations.&nbsp;<\/p>\n\n\n\n<p>Frugone et al. (2021) presented an integrative analysis that suggested negligible hybridization between <em>filholi <\/em>and <em>chrysocome<\/em>, and supported the elevation of <em>filholi <\/em>to species status. Vocalizations (which are incompletely known for <em>filholi<\/em>) appear to be similar but perhaps screechier and less nasal in <em>filholi <\/em>than <em>chrysocome<\/em>, although vocal differentiation (or its lack) between most species of <em>Eudyptes <\/em>remains to be elucidated. Morphological distinctions between two other species of <em>Eudyptes <\/em>(Fiordland <em>Eudyptes pachyrhynchus<\/em> Gray, 1845 and Snares <em>Eudyptes robustus <\/em>Oliver, 1953) are quite similar and equally modest, and the latter was only fairly recently described; nevertheless, these have long generally been considered separate species. Taking all the above into consideration, AviList Core Team (2025) voted to consider <em>filholi <\/em>a separate species. SACC, however<a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1001.htm\">,<\/a> recently <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1001.htm\">voted not to split<\/a> these based on their apparent similarity in vocalizations, shallow genetic divergence, and unclear significance to interbreeding of the main morphological difference, the pale pink skin bordering the lower edge of the mandible and gape in <em>filholi <\/em>that is lacking in <em>chrysocome<\/em>.<\/p>\n\n\n\n<p><strong>English names:<\/strong> When split, the English name Southern Rockhopper Penguin is no longer useful, clear, or apt for either of the component species since <em>chrysocome <\/em>and <em>filholi<\/em> occur at approximately equal latitudes. Nevertheless, Southern Rockhopper Penguin has been widely used for <em>chrysocome <\/em>and Eastern for <em>filholi <\/em>(e.g., Howell and Zufelt 2019, Frugone et al. 2021, Harrison et al. 2021). Because both occur in multiple island groups, and to contrast with Eastern Rockhopper Penguin, already widely familiar for <em>filholi<\/em>, the name Western Rockhopper Penguin has been adopted here.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Cape Verde Petrel <\/strong><strong><em>Pterodroma feae<\/em><\/strong> and <strong>Desertas Petrel <\/strong><strong><em>Pterodroma deserta<\/em><\/strong> are split from <strong>Fea&#8217;s Petrel <\/strong><strong><em>Pterodroma feae<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two petrels that breed only on the Atlantic islands, one on of Bugio in the Desertas and the other on Cape Verde, differ markedly in breeding biology and other aspects, despite their similar plumage.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 7119\u20137120<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Fea&#8217;s Petrel<em> Pterodroma feae<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies: <em>feae <\/em>and<em> deserta<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Cape Verde Petrel<em> Pterodroma feae<\/em> (monotypic)<\/li>\n\n\n\n<li>Desertas Petrel<em> Pterodroma deserta <\/em>(monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/6-Pterodroma-feae-graphical-abstract.png\" alt=\"\" class=\"wp-image-1083 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/6-Pterodroma-feae-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/6-Pterodroma-feae-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/6-Pterodroma-feae-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/6-Pterodroma-feae-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the Atlantic Ocean showing the approximate ranges of the two species into which Fea&#8217;s Petrel <em>Pterodroma feae<\/em> has been partitioned.<\/figcaption><\/figure>\n\n\n\n<p><strong>Map notes<\/strong>: The non-breeding range of <em>feae sensu stricto<\/em> is poorly known, but most individuals appear to remain near the breeding colonies all year, while <em>deserta <\/em>has a far more extensive non-breeding range (indicated by dashed blue line).&nbsp;<\/p>\n\n\n\n<p>The taxonomy of the <em>Pterodroma mollis<\/em> (Gould, 1844) complex has seen major change through the years, with Peters (1931) considering it to comprise two subspecies, the subantarctic <em>mollis <\/em>and <em>feae <\/em>(Salvadori, 1899), the latter taxon breeding on Madeira and the Cape Verdes. Soon afterward, two further taxa were described, <em>deserta <\/em>Mathews, 1934, with type locality Desertas Islands, and <em>madeira <\/em>Mathews, 1934, with type locality Madeira, leaving <em>feae <\/em>restricted to Cape Verde. Mathews (1934a, b) described both <em>deserta <\/em>and <em>madeira <\/em>as subspecies of <em>mollis<\/em>, and also considered <em>feae <\/em>to be a subspecies of <em>mollis<\/em>.<\/p>\n\n\n\n<p>Numerous authors have proposed splitting the <em>mollis <\/em>complex, in various ways (summarized in Jesus et al. 2009). For example, Wolters (1975) treated <em>madeira <\/em>as a distinct species, while considering <em>feae <\/em>a subspecies of <em>mollis<\/em>. Particularly influentially, on the basis of plumage, structure, and vocalizations, Bretagnolle (1995) suggested a two-way division into subantarctic <em>mollis <\/em>vs. the three Macaronesian taxa. This treatment held sway for years, and is further supported by molecular results suggesting <em>mollis <\/em>is not sister to the <em>feae <\/em>clade (Jesus et al. 2009). Zino et al. (2008) argued for the specific separation of <em>deserta <\/em>as well, and Jesus et al. (2009) provided further evidence in support of that treatment. The rationale for the split of <em>deserta <\/em>includes that it is a summer breeder, only on the single island of Bugio, in the Desertas Islands, part of Madeira, where it usually nests in burrows, while <em>feae <\/em>is a winter breeder in the Cape Verde Islands, usually occupying rock crevices. In addition, there are vocal differences between all three (The Sound Approach 2008). Furthermore, the at-sea distributions of <em>deserta<\/em> and <em>feae<\/em> apparently differ dramatically, with <em>deserta <\/em>ranging throughout the Atlantic, as demonstrated by geolocators (Ram\u00edrez et al. 2013, Howell and Zufelt 2019), while <em>feae s.s. <\/em>is evidently largely sedentary, with some reaching waters off Senegal (Milit\u00e3o et al. 2025), although its at-sea range is still unclear. Morphological differences, such as in bill morphology, are however rather slight, and field identification is problematic.<\/p>\n\n\n\n<p>The major difference in breeding season surely forms a temporal barrier to interbreeding, much as in the case of giant-petrels and some storm-petrels. Coupled with the other differences, the specific status of <em>deserta <\/em>was agreed upon by AviList Core Team (2025).&nbsp;<\/p>\n\n\n\n<p><strong>English names:&nbsp; <\/strong>Given fairly similar-sized breeding ranges of the two daughter species (though evidently not of non-breeding ranges) and the potential for confusion due to the fact that the name Fea\u2019s Petrel has been very widely used to refer to what is now known to be <em>deserta<\/em> rather than <em>feae<\/em>, the use of the name Fea\u2019s Petrel is discontinued here. The geographically clarifying names Cape Verde Petrel and Desertas Petrel are adopted for their breeding ranges (as in e.g. Howell and Zufelt 2019). Bugio Petrel, used by Ram\u00edrez et al. (2013), is also an apt name for <em>deserta <\/em>and highlights the importance of its sole breeding island, although it introduces yet another term for this already-confusing complex that does not mirror the specific epithet.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Little Heron <em>Butorides atricapilla<\/em><\/strong> and<strong> Lava Heron <em>Butorides sundevalli<\/em> <\/strong>are split from <strong>Striated Heron <em>Butorides striata<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21923 species) The usually blackish-gray Lava Heron of the Galapagos and the mainly South American Striated Heron, with its distinctive rufous stripe on neck sides, are split from the widely distributed and highly variable Little Heron of the Old World tropics and subtropics, which lacks the rufous-bordered neck stripe, among other differences.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 7669\u20137703<\/p>\n\n\n\n<p>Was:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Striated Heron <em>Butorides striata&nbsp;<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>striata, sundevalli, atricapilla, brevipes, crawfordi, rhizophorae, rutenbergi, degens, didii, albidula, albolimbata, amurensis, actophila, javanica, spodiogaster, carcinophila, steini, moluccarum, papuensis, littleri, idenburgi, flyensis, rogersi, cinerea, stagnatilis, macrorhyncha, solomonensis<\/em>, and <em>patruelis<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Striated Heron <em>Butorides striata<\/em> (monotypic)<\/li>\n\n\n\n<li>Lava Heron <em>Butorides sundevalli<\/em> (monotypic)<\/li>\n\n\n\n<li>Little Heron <em>Butorides atricapilla&nbsp;<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>atricapilla, brevipes, crawfordi, rhizophorae, rutenbergi, degens, didii, albidula, albolimbata, amurensis, actophila, javanica, spodiogaster, carcinophila, steini, moluccarum, papuensis, littleri, idenburgi, flyensis, rogersi, cinerea, stagnatilis, macrorhyncha, solomonensis<\/em>, and <em>patruelis<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/7-Butorides-striata-graphical-abstract.png\" alt=\"\" class=\"wp-image-1084 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/7-Butorides-striata-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/7-Butorides-striata-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/7-Butorides-striata-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/7-Butorides-striata-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the world showing the approximate ranges of the three species into which Striated Heron <em>Butorides striata <\/em>has been partitioned. Only the most common adult plumage type of each species is depicted. <\/figcaption><\/figure>\n\n\n\n<p>While the taxonomic status of the Lava Heron, <em>Butorides sundevalli <\/em>(Reichenow, 1877), of the Galapagos Islands has varied greatly, with many authorities treating it as a full species (including Peters 1931) and many others (including Wolters 1976) as a subspecies. In contrast, until very recently nearly all authors considered <em>Butorides striata<\/em> (Linnaeus, 1758) to be pantropical, with many subspecies. However, Peters (1931) also recognized <em>rogersi <\/em>Mathews, 1911 of northwestern Australia as a full species, as originally described, a treatment since shown to be untenable (as presaged by the comment by Peters that <em>rogersi <\/em>would likely prove to be a color-phase).&nbsp;<\/p>\n\n\n\n<p>Mendales (2023) showed using genomic data that all New World <em>Butorides <\/em>taxa form a clade that is sister to that formed by all sampled Old World taxa, and therefore that the longstanding treatment is untenable. Given that <em>Butorides virescens<\/em> (Linnaeus, 1758) has long been considered a full species largely on the basis of apparent assortative mating (Hayes 2002, Hayes et al. 2013), a four-species treatment of the genus was adopted by AviList Core Team (2025), the most novel one being the split of mainly South American <em>atricapilla <\/em>(Afzelius, 1804), although this was originally described at the species level (long before the invention of subspecies). Further splits (for example a four-way split of Old World taxa into four species: African <em>atricapilla<\/em>, Arabian <em>brevipes<\/em>, Asian <em>javanica<\/em>, and Australasian <em>macrorhyncha <\/em><a href=\"http:\/\/jboyd.net\/Taxo\/List8a.html#ardeiformes\">adopted by J. Boyd<\/a>, among Old World taxa may prove to be justified, but sampling in Mendales (2023) was inadequate to resolve this issue.&nbsp;<\/p>\n\n\n\n<p>Further work on the morphology and taxonomy of the group is in progress (Rasmussen ms). <em>Butorides sundevalli<\/em>, however, though usually blackish, is extraordinarily variable in plumage for a single taxon, especially one with a small range. The many subspecies of the <em>atricapilla <\/em>group together exhibit even greater plumage and size variation, including some dark morphs that strongly resemble <em>sundevalli<\/em>. The South American <em>striata s.s<\/em>., in contrast, is monotypic and is much less variable in plumage over its wide range, though a few individuals south to Argentina have a brownish-rufous rather than gray neck.&nbsp; See under Changes to Groups section for division of Old World taxa in <em>Butorides atricapilla<\/em> into groups.<\/p>\n\n\n\n<p>Notably, in contrast to the other New World taxa, <em>sundevalli <\/em>is nearly restricted to rocky coastlines and adjacent mangroves (and has adapted to coastal human structures). Some Old World taxa (e.g. <em>brevipes <\/em>of the Persian Gulf region and the Australian taxa) are largely restricted to coastlines and mangroves, while most other taxa are typically found inland.<\/p>\n\n\n\n<p>The specific status of Green Heron <em>Butorides virescens <\/em>is also open to question, and it has often been considered conspecific with its congeners (e.g. in Wolters 1976), but is treated as a full species by AOS, based partly on Hayes (2002) and Hayes et al. (2013).<\/p>\n\n\n\n<p><strong>English names: <\/strong>The previously used names Striated, Lava, and Little Herons are used for South American <em>striata s.s.<\/em>, Galapagos <em>sundevalli<\/em>, and Old World <em>atricapilla<\/em>, respectively. However, further work is needed to establish more useful and less confusing names than Striated and Little Herons.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Coppery-tailed Trogon <\/strong><strong><em>Trogon ambiguus<\/em><\/strong><em> <\/em>is split from <strong>Elegant Trogon <\/strong><strong><em>Trogon elegans<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two trogons that are widely separated by the Isthmus of Tehuantepec in southern Mexico differ in plumage and somewhat in voice, and are now considered separate species.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 9569\u20139575<\/p>\n\n\n\n<p>Was:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Elegant Trogon <em>Trogon elegans<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>canescens, goldmani, ambiguus, elegans<\/em>, and <em>lubricus<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Coppery-tailed Trogon <em>Trogon ambiguus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>canescens, goldmani<\/em>, and <em>ambiguus<\/em><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Elegant Trogon <em>Trogon elegans<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>elegans <\/em>and <em>lubricus<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/8-Trogon-elegans-graphical-abstract.png\" alt=\"\" class=\"wp-image-1085 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/8-Trogon-elegans-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/8-Trogon-elegans-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/8-Trogon-elegans-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/8-Trogon-elegans-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of Mexico and Central America showing the approximate ranges of the two species into which Elegant Trogon <em>Trogon elegans<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Although lumped by nearly all authorities since Peters (1945), with the exception of Oberholser (1974), the broadly allopatric Mesoamerican <em>Trogon ambiguus<\/em> Gould, 1835, occurring in Mexico north of the Isthmus of Tehuantepec and marginally in the southwestern USA, and <em>Trogon elegans <\/em>Gould, 1834 groups of Central America south to northwestern Costa Rica were again treated as separate species by del Hoyo and Collar (2014). This split was based on plumage differences: adult males of the two forms differ in undertail pattern and uppertail color, as well as (more subtly) in wing covert vermiculation. Furthermore, they differ (with some overlap, and with no formal vocal analysis yet) in primary vocalizations, the song of <em>ambiguus <\/em>being typically delivered at a faster rate than that of <em>elegans <\/em>(Remsen 2022, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2022\/04\/2022-A-final.pdf\">NACC proposal set 2022-A<\/a>).&nbsp;<\/p>\n\n\n\n<p>Dyer and Howell (2023) treated the two as specifically distinct on the basis of plumage and voice. However, given that no comprehensive vocal analysis has been done, the apparent within-taxon variation in voice, rather minor mtDNA differentiation (DaCosta and Klicka 2008), and the known intergradation of other <em>Trogon <\/em>taxa with similar levels of plumage variation, the above NACC proposal did not pass. AviList Core Team (2025), however, considered that the balance of evidence favors the two-species treatment.<\/p>\n\n\n\n<p><strong>English names: <\/strong>The English names that have been fairly broadly adopted for the two daughter species are tentatively adopted. However, some degree of confusion is likely to result due to the retention of the name Elegant Trogon for the southern daughter species <em>Trogon elegans<\/em>, and further consideration is needed.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Pale-mandibled Aracari<\/strong><strong><em> Pteroglossus erythropygius<\/em><\/strong><em> <\/em>is split from <strong>Collared Aracari<\/strong><strong><em> Pteroglossus torquatus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two aracaris that hybridize in a narrow zone in far northern Colombia differ in bill structure and in genetics, and are now considered separate species, the Collared Aracari in Middle America and northern South America, and the Pale-mandibled Aracari in northwestern South America.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 10885\u201310891<\/p>\n\n\n\n<p>Was:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Collared Aracari<em> Pteroglossus torquatus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>torquatus, erythrozonus, nuchalis<\/em>,<em> sanguineus<\/em>, and <em>erythropygius<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Collared Aracari<em> Pteroglossus torquatus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>torquatus, erythrozonus, <\/em>and <em>nuchalis<\/em><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Pale-mandibled Aracari<em> Pteroglossus erythropygius<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>sanguineus<\/em> and <em>erythropygius<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical Abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/9-Pteroglossus-torquatus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1086 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/9-Pteroglossus-torquatus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/9-Pteroglossus-torquatus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/9-Pteroglossus-torquatus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/9-Pteroglossus-torquatus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the northern Neotropics showing the approximate ranges of the two species into which Collared Aracari <em>Pteroglossus torquatus <\/em>is partitioned. Species border is delimited by gray dashed line.<\/figcaption><\/figure>\n\n\n\n<p>The Collared Aracari <em>Pteroglossus torquatus <\/em>(Gmelin, 1788) is the most widely distributed member of its genus in Mesoamerica, and four component taxa also reach northwestern South America. In addition, the closely related Fiery-billed Aracari <em>Pteroglossus franzii <\/em>Cabanis, 1861 occurs in southwestern Central America. Peters (1948) treated the complex as comprising three species, with <em>frantzii <\/em>a subspecies of <em>torquatus<\/em>, and the two primarily western South American taxa <em>sanguineus <\/em>Gould, 1854 and <em>erythropygius <\/em>Gould, 1843 as separate species. Haffer (1974), followed by Wolters (1976), treated all these as subspecies of <em>torquatus<\/em>, based largely on evidence of hybridization, although the hybrid zone (which Haffer 1974 called \u2018uninhibited\u2019) in southeastern Panama between <em>torquatus <\/em>and <em>sanguineus <\/em>appears to be narrow, and no hybrid zone is known between <em>torquatus <\/em>and <em>frantzii<\/em>, which instead appear to be parapatric or even narrowly sympatric. Hybridization between <em>erythropygius <\/em>and <em>sanguineus <\/em>in northwestern Ecuador appears to be common (Short and Horne 2001), and this seems to be borne out in ML photos. AOS (1998) treated <em>erythropygius <\/em>as a species but not <em>sanguineus<\/em>. Several other authors have treated all as separate species (e.g., Ridgely and Greenfield 2001), without providing detailed rationale.<\/p>\n\n\n\n<p>In a phylogeny based on mtDNA and a nuclear intron (Patel et al. 2011), <em>frantzii <\/em>is sister to a clade formed by <em>erythropygius <\/em>and <em>sanguineus<\/em>, with <em>torquatus <\/em>sister to these two clades. Morphologically, <em>frantzii <\/em>is the most distinctive in plumage, while it and <em>erythropygius <\/em>and <em>sanguineus <\/em>differ conspicuously from the <em>torquatus <\/em>group in the number and development of tomial \u2018teeth\u2019. <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop112.htm\">SACC last considered this issue in 2004<\/a> and narrowly rejected it then. AviList Core Team (2025) takes a two-species approach, as outlined above, and in addition continues to recognize <em>frantzii <\/em>as a full species.<\/p>\n\n\n\n<p><strong>English names: <\/strong>The<strong> <\/strong>English name Pale-mandibled Aracari tentatively adopted for one daughter species has a history of use (del Hoyo and Collar 2014). However, given that here the species <em>Pteroglossus erythropygius <\/em>also includes the taxon <em>sanguineus<\/em>, which has a dark mandible, it is only apt for taxon <em>erythropygius<\/em>, and further consideration is needed.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Cliff Parakeet <\/strong><strong><em>Myiopsitta luchsi<\/em><\/strong> is<em> <\/em>split from <strong>Monk Parakeet <\/strong><strong><em>Myiopsitta monachus<\/em><\/strong>&nbsp;<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Bolivia gains a new endemic with the split of the Cliff Parakeet from the widespread Monk Parakeet of central and southern South America, from which it differs in breeding habits and voice.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 12819\u201312822<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Monk Parakeet <em>Myiopsitta monachus<\/em><\/li>\n\n\n\n<li>subspecies <em>cotorra, monachus, calita<\/em>, and <em>luchsi<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Monk Parakeet <em>Myiopsitta monachus<\/em><\/li>\n\n\n\n<li>subspecies <em>cotorra, monachus<\/em>, and <em>calita<\/em><\/li>\n\n\n\n<li>Cliff Parakeet <em>Myiopsitta luchsi<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract<\/strong>:<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/10-Myiopsitta-luchsi-graphical-abstract.png\" alt=\"\" class=\"wp-image-1087 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/10-Myiopsitta-luchsi-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/10-Myiopsitta-luchsi-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/10-Myiopsitta-luchsi-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/10-Myiopsitta-luchsi-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of southern South America showing the approximate ranges of the two species into which Monk Parakeet <em>Myiopsitta monachus<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Throughout most of its wide range in southern South America (and locally in North America, Europe, Israel, and elsewhere as a result of introductions), the Monk Parakeet <em>Myiopsitta monachus<\/em> (Boddaert, 1783) is well-known for its remarkable communal stick nests that are normally placed in trees, or these days on power poles and the like. In contrast, in central Bolivia, the taxon <em>luchsi <\/em>(Finsch, 1868) (which was originally described as a species) builds similar communal nests but exclusively on cliff faces, even where trees are present. In addition, <em>luchsi <\/em>differs consistently from the other taxa in plumage, especially its unscaled breast; in its vocalizations (though no published vocal analysis exists); in mtDNA (Russello et al. 2008); and in UCE data (Smith et al. 2023). Furthermore, evidence of hybridization is not known despite their parapatry. Although two earlier proposals to SACC failed, as did the first one to AviList, the accumulation of further evidence, especially sound recordings, has led to its specific status now being accepted by both <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1021.htm\">SACC<\/a> and AviList Core Team (2025).&nbsp;<\/p>\n\n\n\n<p><strong>English names: <\/strong>The names adopted here, Cliff Parakeet and Monk Parakeet, have been widely used previously. In addition, Cliff Parakeet aptly describes the breeding habitat chosen by this taxon, in strong contrast to that of the Monk Parakeet, a very familiar and deeply embedded name for this widespread species.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Red-lored Amazon<\/strong><strong><em> Amazona autumnalis<\/em><\/strong><strong>, Lilacine Amazon<\/strong><strong><em> Amazona lilacina<\/em><\/strong>, and <strong>Diademed Amazon <\/strong><strong><em>Amazona diadema<\/em><\/strong> are split from <strong>Red-lored Amazon<\/strong><strong><em> Amazona autumnalis<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21923 species) One of the most familiar amazons in Middle America, the Red-lored Amazon, is much less so in the Ecuador and Brazil populations, and these two little-known isolates are now considered separate species, the Lilacine and Diademed amazons.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 12909\u201312915<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Red-lored Amazon<em> Amazona autumnalis<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>autumnalis<\/em>, <em>salvini<\/em>, <em>lilacina<\/em>, and <em>diadema<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Red-lored Amazon<em> Amazona autumnalis<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>autumnalis <\/em>and <em>salvini<\/em><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Lilacine Amazon<em> Amazona lilacina<\/em> (monotypic)<\/li>\n\n\n\n<li>Diademed Amazon <em>Amazona diadema<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract<\/strong>:<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/11-Amazona-autumnalis-graphical-abstract.png\" alt=\"\" class=\"wp-image-1088 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/11-Amazona-autumnalis-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/11-Amazona-autumnalis-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/11-Amazona-autumnalis-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/11-Amazona-autumnalis-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the northern Neotropics showing the approximate ranges of the three species into which Red-lored Amazon <em>Amazona autumnalis<\/em> is partitioned. The approximate zone of intergradation between <em>autumnalis<\/em> and <em>salvini<\/em> is indicated by dashed lines. Range of <em>lilacina<\/em> shown in orange is that of current roost sites (Biddle et al. 2020).<\/figcaption><\/figure>\n\n\n\n<p>Four taxa treated by most authorities (including Wolters 1975) as conspecific under <em>Amazona autumnalis<\/em> (Linnaeus, 1758) at least since Peters (1937) were originally described as full species: <em>autumnalis<\/em> of Mexico to northern Central America; <em>salvini <\/em>(Salvadori, 1891) of central Central America to northern South America; <em>lilacina <\/em>Lesson, 1844 of coastal Ecuador; and <em>diadema <\/em>(Spix, 1824) of a limited area in central Amazonia. While <em>autumnalis <\/em>and <em>salvini <\/em>are common and well-known, <em>diadema <\/em>is a rather mysterious and broadly allopatric Amazonian taxon, and <em>lilacina <\/em>is a rather rare and local mangrove-roosting species of coastal southwestern Ecuador (Freile and Restall 2018) that may be parapatric with <em>salvini <\/em>(Donegan et al. 2016), although current roost sites are well south of the range of <em>salvini <\/em>(Biddle et al. 2020), and reports from northwestern Ecuador require validation.<\/p>\n\n\n\n<p>Based largely on multiple morphological differences, del Hoyo and Collar (2014) considered there to be three species in the complex, in splitting both <em>lilacina <\/em>and <em>diadema<\/em>. Genetic data are contradictory and thus inconclusive (Ottens-Wainright et al. 2004, Russello and Amato 2004, Pilgrim 2010, Smith et al. 2023). A recent <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1009.htm\">proposal to SACC narrowly failed<\/a>, but the three-way split was adopted by AviList Core Team (2025).&nbsp;<\/p>\n\n\n\n<p><strong>English names: <\/strong>The previously used English names (del Hoyo and Collar 2014) of Red-lored Amazon, Lilacine Amazon, and Diademed Amazon for the daughter and parent species were tentatively adopted.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Painted Parakeet <em>Pyrrhura picta<\/em> <\/strong>is split into four species<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21924 species) The colorful Painted Parakeet is now treated as four species, most of which are narrow endemics in northern South America.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 13034\u201313039<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Painted Parakeet <em>Pyrrhura picta<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>eisenmanni, subandina, caeruleiceps, emma<\/em>, and <em>picta<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Subandean Parakeet <em>Pyrrhura subandina<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>eisenmanni<\/em> and <em>subandina<\/em><\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Perija Parakeet <em>Pyrrhura caeruleiceps<\/em> (monotypic)<\/li>\n\n\n\n<li>Venezuelan Parakeet <em>Pyrrhura emma<\/em> (monotypic)<\/li>\n\n\n\n<li>Painted Parakeet <em>Pyrrhura picta<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract<\/strong>:<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/12-Pyrrhura-picta-graphical-abstract.png\" alt=\"\" class=\"wp-image-1089 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/12-Pyrrhura-picta-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/12-Pyrrhura-picta-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/12-Pyrrhura-picta-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/12-Pyrrhura-picta-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of northern South America showing the approximate ranges of the four species into which Painted Parakeet <em>Pyrrhura picta<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Few avian taxa have as complicated taxonomic histories as do the Neotropical <em>Pyrrhura <\/em>parakeets, as illustrated by <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop306.htm\">a 2007 SACC proposal to split<\/a> the <em>P. picta <\/em>(M\u00fcller, 1776) and <em>P. leucotis <\/em>complexes, based partly on Ribas et al. (2006). Despite this rearrangement, subsequent molecular work (Smith et al. 2023) indicates that the current treatment of the <em>picta <\/em>complex of northern South America and southwestern Panama involves several cases of non-monophyly with other taxa normally considered different species. Differences in plumage and iris color between these broadly allopatric taxa further suggest the necessity of taxonomic revision.&nbsp;<\/p>\n\n\n\n<p>Uncertainty remains, particularly with respect to the treatment of the taxon <em>eisenmanni<\/em> Delgado, 1985 of the Azuero Peninsula, south-central Panama, as conspecific with the taxon <em>subandina <\/em>Todd, 1917 of the Sin\u00fa Valley of northwestern Colombia (the latter now perhaps extinct). Nevertheless, a four-species treatment has been adopted by AviList Core Team (2025): <em>subandina<\/em>; <em>picta <\/em>(of the Guianan Shield to Brazil north of the Amazon River); <em>emma <\/em>(of northern Venezuela); and <em>caeruleiceps <\/em>(of the Perij\u00e1 Mountains on the border of northeastern Colombia and northwestern Venezuela).&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> Three of the English names used by del Hoyo and Collar (2014) for the split taxa are tentatively adopted here: Painted Parakeet for <em>Pyrrura picta s.s<\/em>.; Venezuelan Parakeet for <em>Pyrrhura emma<\/em>; and Perija Parakeet for <em>Pyrrhura caeruleiceps<\/em>. The latter two seem uncontroversial and apt, while retention of the former (Painted) for just one of the isolates may lead to confusion. An alternative suggestion would be Guianan Parakeet for <em>P. picta s.s.<\/em>, although its range extends somewhat beyond this region. For the combined species <em>subandina <\/em>and <em>eisenmanni<\/em>, no very apt name has been found and the name Subandean Parakeet, which mirrors the species epithet, is tentatively used but is not a good fit for Panamanian <em>eisenmanni<\/em>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Mara\u00f1on Antshrike <\/strong><strong><em>Thamnophilus shumbae<\/em><\/strong> is split from <strong>Collared Antshrike <\/strong><strong><em>Thamnophilus bernardi<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The Mara\u00f1on Antshrike from its namesake valley in Peru sings a much faster song than the closely related Collared Antshrike, despite occurring in close proximity.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 13532\u201313533<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Collared Antshrike <em>Thamnophilus bernardi<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>bernardi<\/em> and <em>shumbae<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Collared Antshrike <em>Thamnophilus bernardi<\/em> (monotypic)<\/li>\n\n\n\n<li>Mara\u00f1on Antshrike <em>Thamnophilus shumbae<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract<\/strong>:<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/13-Thamnophilus-bernardi-graphical-abstract.png\" alt=\"\" class=\"wp-image-1090 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/13-Thamnophilus-bernardi-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/13-Thamnophilus-bernardi-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/13-Thamnophilus-bernardi-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/13-Thamnophilus-bernardi-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of western South America showing the ranges of the two species into which Collared Antshrike <em>Thamnophilus bernardi <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>A notable difference in song pace between <em>Thamnophilus bernardi<\/em> Lesson, 1844 mainly of western Ecuador and western Peru, and the inland taxon <em>shumbae <\/em>(Carriker, 1934) from the Mara\u00f1\u00f3n Valley of northern Peru is well-known (Schulenberg et al. 2007, Boesman 2016: 54). This, coupled with plumage differences, would seem to be sufficient for species rank in this group in which vocalizations are key. Although <em>shumbae <\/em>was originally described as a subspecies of <em>bernardi<\/em> and treated as such nearly universally, including by Peters (1951), it was elevated by del Hoyo and Collar (2016) to species status. However, the situation is complicated by intrusion of <em>bernardi <\/em>into the Mara\u00f1\u00f3n Valley as well, leading to uncertainty as to the nature of their interactions, and more recently by evidence for considerable gene flow between them by Oswald et al. (2017). This led to initial failure of the AviList motion to split <em>shumbae<\/em>.<\/p>\n\n\n\n<p>However, unpublished data indicating parapatry and lack of response to playback to each others\u2019 songs, with strong response to their own songs (Zimmer, in <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1000.htm\">SACC proposal 1000<\/a>, which narrowly failed) eventually led to the conclusion upon a revote by AviList Core Team (2025) that <em>shumbae <\/em>and <em>bernardi <\/em>are best treated as separate species.<\/p>\n\n\n\n<p><strong>English names:<\/strong> The long-standing, familiar name Collared Antshrike remains the best choice for <em>bernardi<\/em>, while the name Maranon Antshrike as used by del Hoyo and Collar (2016) for <em>shumbae<\/em>, but standardized as Mara\u00f1on for consistency with other taxa thus named in the eBird\/Clements checklist, is tentatively adopted here.&nbsp;<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Black-capped Antthrush <\/strong><strong><em>Formicarius nigricapillus<\/em><\/strong> and <strong>Black-hooded Antthrush <\/strong><strong><em>Formicarius destructus<\/em><\/strong> are split from <strong>Black-headed Antthrush <\/strong><strong><em>Formicarius nigricapillus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Southern Central America and the Choc\u00f3 region of northwestern South America each gain another difficult-to-see endemic, with the split of the Black-capped Antthrush from the Black-hooded Antthrush.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 14492\u201314493<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Black-headed Antthrush <em>Formicarius nigricapillus<\/em>\n<ul class=\"wp-block-list\">\n<li>subspecies <em>nigricapillus<\/em> and <em>destructus<\/em><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Black-capped Antthrush <em>Formicarius nigricapillus<\/em> (monotypic)<\/li>\n\n\n\n<li>Black-hooded Antthrush <em>Formicarius destructus<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/14-Formicarius-nigricapillus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1091 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/14-Formicarius-nigricapillus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/14-Formicarius-nigricapillus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/14-Formicarius-nigricapillus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/14-Formicarius-nigricapillus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of Central and northern South America showing the ranges of the two species into which Black-headed Antshrike <em>Formicarius nigricapillis <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Two disjunct antthrush taxa long treated as conspecific (at least since Peters 1951), <em>Formicarius nigricapillus<\/em> Ridgway, 1893 of montane Costa Rica and Panama, and <em>destructus <\/em>Hartert, 1898 of lowlands of the Choc\u00f3 bioregion of northwestern South America, have been shown to differ in plumage, morphometrics, and song (Areta and Ben\u00edtez Sald\u00edvar 2025). The form <em>destructus <\/em>(so named because the type specimen was \u201cvery much destroyed by the shot\u201d; Hartert 1898) was originally described as a subspecies of <em>Formicarius analis<\/em> (in which species Hartert also placed <em>nigricapillus<\/em>), but has been considered a subspecies of <em>nigricapillus<\/em> since at least Chapman (1917), and was thus treated by the influential Peters (1951). Only rarely has <em>destructus <\/em>been considered a full species (Salvadori and Festa 1899, Howell and Dyer 2022). However, following the comprehensive analysis by Areta and Ben\u00edtez Sald\u00edvar (2025), <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1044.htm\">SACC<\/a>, NACC (Areta and Ben\u00edtez Sald\u00edvar 2025, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/05\/2025-D.pdf\">2025-D-2<\/a>), and AviList Core Team (2025) have all accepted the split.<\/p>\n\n\n\n<p><strong>English names: <\/strong>The retention of the name Black-headed Antthrush for either daughter species has been deemed unsatisfactory in this case, given their approximately similar-sized distributions and levels of familiarity. However, the subtlety of distinguishing phenotypic characteristics, and the presence of other antthrush species in their ranges has made <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1044B.htm\">decisions about English names difficult<\/a>. The names ultimately agreed upon by SACC and thus adopted here, Black-capped Antthrush for <em>Formicarius nigricapillus s.s.<\/em> and Black-hooded Antthrush for <em>Formicarius destructus<\/em>, reflect differences in their plumage, and the former mirrors the specific epithet.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Creamy-breasted Canastero <em>Asthenes dorbignyi<\/em><\/strong> is split into three species<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21923 species) Peru is the epicenter of diversity of the former Creamy-breasted Canastero, and multiple species have long been known from there, of which we recognize three, and await the description of two others.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 15375\u201315382<\/p>\n\n\n\n<p>Was:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Creamy-breasted Canastero <em>Asthenes dorbignyi<\/em><\/li>\n\n\n\n<li>subspecies <em>huancavelicae, arequipae, usheri, consobrina<\/em>, and <em>dorbignyi<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pale-tailed Canastero <em>Asthenes huancavelicae<\/em><\/li>\n\n\n\n<li>subspecies <em>huancavelicae<\/em> and <em>usheri<\/em><\/li>\n<\/ul>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Dark-winged Canastero <em>Asthenes arequipae<\/em> (monotypic)<\/li>\n\n\n\n<li>Rusty-vented Canastero <em>Asthenes dorbignyi<\/em><\/li>\n\n\n\n<li>subspecies <em>consobrina<\/em> and <em>dorbignyi<\/em><\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/15-Asthenes-dorbignyi-graphical-abstract.png\" alt=\"\" class=\"wp-image-1092 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/15-Asthenes-dorbignyi-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/15-Asthenes-dorbignyi-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/15-Asthenes-dorbignyi-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/15-Asthenes-dorbignyi-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the three species into which Creamy-breasted Canastero <em>Asthenes dorbignyi<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Few species complexes are beset by as many as two long-undescribed taxa, as in the case of the Creamy-breasted Canastero <em>Asthenes dorbignyi<\/em>. All taxa were treated as conspecific by Peters (1951): <em>huancavelica <\/em>Morrison, 1938; <em>usheri <\/em>Morrison, 1947; <em>arequipae <\/em>(Sclater &amp; Salvin, 1869); <em>consobrina <\/em>Hellmayr, 1925; and <em>dorbignyi <\/em>(Reichenbach, 1853), to the exclusion of the western Bolivian <em>Asthenes berlepschi <\/em>(Hellmayr, 1917).&nbsp;<\/p>\n\n\n\n<p>&nbsp;&nbsp;The situation is <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop27.htm\">described in the early SACC proposal<\/a>, in which near-certainty about multiple species being involved was expressed but the proposal failed due to the details remaining unpublished. That there are at least two unnamed taxa in the complex and that all taxa are believed to be allopatric, parapatric, or altitudinally segregated was indicated by Fjelds\u00e5 and Krabbe (1990). Additionally, they are considered to differ vocally and to lack evidence of intergradation (Fjelds\u00e5 and Krabbe 1990, Boesman 2016: 96). Ridgely and Tudor (1994) treated the complex as comprising three described species, and they were followed in this by the IOC-WBL from v.1.0, while del Hoyo and Collar (2016) treated the described taxa of the complex as comprising four species. Harvey et al. (2020) showed on the basis of genomic data that the longstanding single-species treatment of this complex to the exclusion of <em>Asthenes berlepschi<\/em> (Hellmayr, 1917) [which is narrowly allopatric in the Upper R\u00edo Consata drainage, in La Paz, western Bolivia, and was said by Fjelds\u00e5 and Krabbe (1990) to possibly be best treated as a subspecies of <em>arequipae<\/em>] creates an instance of paraphyly.&nbsp;<\/p>\n\n\n\n<p>Given that a three-species treatment of the described taxa is surely closer to the best solution than is the unjustified lump of all, which would have to include <em>berlepschi<\/em>, AviList Core Team (2025) agreed to an interim three-way split of the erstwhile <em>dorbignyi s.l<\/em>. Thus, the species here recognized are:&nbsp;<\/p>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Pale-tailed Canastero <em>Asthenes huancavelicae<\/em>, with subspecies <em>huancavelicae<\/em> (of the R\u00edo Mantaro drainage of Huancavelica and western Ayacucho, central Peru at about 3350\u20133700 m) and <em>usheri<\/em> (of the Pampas and upper Apur\u00edmac drainages of south-central Peru in northeastern Ayacucho, Apur\u00edmac, and southwestern Cusco, at 2150\u20133800 m (Schulenberg et al. 2007);<\/li>\n\n\n\n<li>Dark-winged Canastero <em>Asthenes arequipae <\/em>of the western slope of the Andes of southwestern Peru of Lima and Ayacucho southward to western Bolivia and northern Chile; and<\/li>\n\n\n\n<li>Rusty-vented Canastero <em>Asthenes dorbignyi<\/em>, with subspecies <em>consobrina<\/em> of the Andes of northwestern Bolivia, and subspecies <em>dorbignyi<\/em> of the Andes from central Bolivia to northwestern Argentina.<\/li>\n<\/ol>\n\n\n\n<p>In addition, there are undescribed taxa, one each presumably in the species delineated as <em>huancavelica <\/em>and <em>arequipae <\/em>(Fjelds\u00e5 and Krabbe 1990).&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> The English names tentatively adopted have been in long usage at least since the publication of Fjelds\u00e5 and Krabbe (1990), and are reasonably apt and utilitarian for these subtly plumaged taxa.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Vilcabamba Spinetail <\/strong><strong><em>Cranioleuca weskei<\/em><\/strong><strong> <\/strong>is split from <strong>Marcapata Spinetail<\/strong><strong><em> Cranioleuca marcapatae<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two central Peruvian spinetails with strikingly colored crowns, one white and the other one bright chestnut, seem not to mix despite close approach, and are thus now considered species.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 15485\u201315486<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Marcapata Spinetail <em>Cranioleuca marcapatae<\/em><\/li>\n\n\n\n<li>subspecies <em>marcapatae<\/em> and <em>weskei<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Marcapata Spinetail <em>Cranioleuca marcapatae<\/em> (monotypic)<\/li>\n\n\n\n<li>Vilcabamba Spinetail <em>Cranioleuca weskei<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/16-Cranioleuca-marcapatae-graphical-abstract.png\" alt=\"\" class=\"wp-image-1093 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/16-Cranioleuca-marcapatae-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/16-Cranioleuca-marcapatae-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/16-Cranioleuca-marcapatae-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/16-Cranioleuca-marcapatae-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of Peru showing the ranges of the two species into which Marcapata Spinetail <em>Cranioleuca marcapatae <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>The taxon <em>Cranioleuca marcapatae <\/em>Zimmer, 1935 is limited in distribution to a narrow zone in central Cusco, while the recently described <em>weskei <\/em>Remsen, 1984 is now known to be found more widely in south-central Peru (including the Mantaro Valley in southeastern Jun\u00edn, northern Ayacucho, and southward to Cordillera Vilcabamba in Cusco). Although earlier thought to be widely allopatric, the two occur within some 40 km of each other (Seeholzer in <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1010.htm\">SACC proposal 1010<\/a>), and the intervening valleys do not appear to present an insurmountable barrier based on the distribution of <em>weskei<\/em> across other river valleys. While the initial treatment of <em>weskei <\/em>as a subspecies was based partly on analogy of crown color variation from rufous to white in the related <em>Cranioleuca albiceps<\/em> (d&#8217;Orbigny &amp; de Lafresnaye, 1837), and the expectation that such would likely be found to be the case with <em>weskei <\/em>and <em>marcapatae<\/em>, that has not proven to be the case, with photos of even those individuals nearest each others\u2019 ranges <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1010.htm\">being clearly white or clearly rufous<\/a>. However, reports of possible intergradation (Hosner et al. 2015) over a narrow zone require further study.<\/p>\n\n\n\n<p>In addition, differences in vocalizations have been documented (Boesman 2016: 100), although intrataxon variation and sample sizes are a problem, and further study is also required on this aspect. On the basis of phenotypic and vocal differences, del Hoyo and Collar (2016) treated <em>weskei <\/em>as a separate species from <em>marcapatae<\/em>. This is now the treatment adopted by SACC and AviList Core Team (2025).&nbsp;<\/p>\n\n\n\n<p><strong>English names: <\/strong>Given their respective river-valley distributions, the names Marcapata Spinetail for <em>Cranioleuca marcapatae<\/em> and Vilcabamba Spinetail for <em>Cranioleuca weskei, <\/em>which were used by del Hoyo and Collar (2016), have been adopted by SACC and followed here. Nevertheless, confusion due to the retention of the parent species name for one of the daughter species is possible, but seems not to be a major problem, as both taxa are narrowly distributed within one region of a single country, Peru.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Blue Mountain Elaenia <\/strong><strong><em>Elaenia fallax<\/em><\/strong> and <strong>Hispaniolan Elaenia<\/strong><strong><em> Elaenia cherriei<\/em><\/strong> are split from <strong>Greater Antillean Elaenia <\/strong><strong><em>Elaenia fallax<\/em><\/strong>&nbsp;<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two West Indian islands now each host yet another endemic bird species, with the split of Greater Antillean Elaenia into Blue Mountain Elaenia and Hispaniolan Elaenia.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 16743\u201316744<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Greater Antillean Elaenia <em>Elaenia fallax<\/em><\/li>\n\n\n\n<li>subspecies <em>fallax<\/em> and <em>cherriei<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Blue Mountain Elaenia <em>Elaenia fallax<\/em> (monotypic)<\/li>\n\n\n\n<li>Hispaniolan Elaenia <em>Elaenia cherriei<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/17-Elaenia-fallax-graphical-abstract.png\" alt=\"\" class=\"wp-image-1094 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/17-Elaenia-fallax-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/17-Elaenia-fallax-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/17-Elaenia-fallax-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/17-Elaenia-fallax-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the Greater Antilles showing the ranges of the two species into which Greater Antillean Pewee <em>Elaenia fallax <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Among elaenias of the genus <em>Elaenia<\/em>, morphological differences are typically minimal. Thus the long-term (since Hellmayr 1927, continued by Traylor 1979 in volume 8 of the Peters Check-list) retention of the diagnosably different <em>Elaenia cherrei<\/em> Cory, 1895 of Hispaniolan hills as conspecific with <em>Elaenia fallax<\/em> Sclater, 1861 of Jamaican highlands requires reevaluation. del Hoyo and Collar (2016) were the first in many years to treat the two as separate species, citing molecular divergence (Rheindt et al. 2008), morphology, and vocal differences among a small sample. With the benefit of the much larger sample of online recordings now available, AviList Core Team (2025) agreed to a two-species treatment. However, a 2022 proposal to NACC (Stotz 2022, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2022\/04\/2022-C.pdf\">2022-C-15<\/a>) failed, largely on the basis that vocal comparisons remain unpublished, and appear to be in conflict with statements about vocalizations in e.g. Kirwan et al. (2019, 2021), as well as lack of agreement on the species-delimitation value of genetic divergence and the often-higher levels of divergence between insular taxa than mainland ones.<\/p>\n\n\n\n<p><strong>English names: <\/strong>As there is already a taxon known long and widely as the Jamaican Elaenia <em>Myiopagis cotta<\/em> (Gosse, 1849), this name is not an option for the split <em>fallax<\/em>. However, despite the failure of the proposal to pass NACC, the name Blue Mountain Elaenia for this highland species found wide favor, and is tentatively adopted here for <em>fallax s.s<\/em>. Hispaniolan Elaenia seems a non-controversial name for <em>cherrei<\/em>, and is also tentatively adopted here. del Hoyo and Collar (2016), however, used Large Jamaican Elaenia for <em>Elaenia fallax s.s<\/em>. and Small Jamaican Elaenia for <em>Myiopagis cotta<\/em>, but this suggests a close relationship that does not exist. <a href=\"http:\/\/john-boyd.com\/Taxo\/changes.html\">J. Boyd suggested the eponym Sclater\u2019s Elaenia<\/a> for <em>Elaenia fallax s.s<\/em>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Salvadoran Flycatcher <\/strong><strong><em>Myiarchus flavidior<\/em><\/strong> is split from <strong>Nutting&#8217;s Flycatcher <\/strong><strong><em>Myiarchus nuttingi<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Yet another difficult-to-identify flycatcher species is now recognized, the Salvadoran Flycatcher, which can however best be identified by its distinctive voice.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 17326\u201317329<\/p>\n\n\n\n<p>Was:&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Nutting&#8217;s Flycatcher <em>Myiarchus nuttingi<\/em><\/li>\n\n\n\n<li>subspecies <em>inquietus, nuttingi<\/em>, and <em>flavidior<\/em>&nbsp;<\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Nutting&#8217;s Flycatcher <em>Myiarchus nuttingi<\/em><\/li>\n\n\n\n<li>subspecies <em>inquietus<\/em> and <em>nuttingi<\/em><\/li>\n\n\n\n<li>Salvadoran Flycatcher <em>Myiarchus flavidior<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/18-Myiarchus-nuttingi-graphical-abstract.png\" alt=\"\" class=\"wp-image-1095 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/18-Myiarchus-nuttingi-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/18-Myiarchus-nuttingi-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/18-Myiarchus-nuttingi-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/18-Myiarchus-nuttingi-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of Mexico and Central America showing the ranges of the two species into which Nutting&#8217;s Flycatcher <em>Myiarchus nuttingi <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Another of the most taxonomically fraught genera in Class Aves (comparable to <em>Elaenia<\/em>) is <em>Myiarchus<\/em>, whose taxonomy was greatly improved by the pioneering and comprehensive field and museum studies of W. E. Lanyon, when sound recording was much more difficult than it is today. One of the many taxonomic conundra Lanyon resolved was the demonstration of specific distinctness of the Middle American Nutting\u2019s Flycatcher <em>Myiarchus nuttingi<\/em> Ridgway, 1882 (originally described as a species) from Ash-throated Flycatcher <em>Myiarchus cinerascen<\/em>s (Lawrence, 1851) (Lanyon 1961). His recommended treatment of a three-subspecies <em>Myiarchus nuttingi<\/em> (including <em>nuttingi<\/em>, <em>flavidior<\/em>, and <em>inquietus <\/em>Salvin &amp; Godman, 1889) distributed from northern Mexico to northwestern Costa Rica was followed by Traylor (1979), in the eighth volume of the Peters Check-list, and thus by subsequent authorities.&nbsp;<\/p>\n\n\n\n<p>However, further problems remained in the complex that were beyond the scope of Lanyon\u2019s (1961) study, as highlighted by Howell (2012), who considered that two species must be involved in <em>M. nuttingi<\/em>. After much further fieldwork and related study, Howell et al. (2024) have shown that the taxon <em>flavidior <\/em>Van Rossem, 1936, which was described as a subspecies of <em>cinerascens <\/em>and then placed in <em>M. nuttingi<\/em>, is diagnosably different in plumage and habitat, and has some quite distinct vocalizations. Additionally, Howell et al.\u2019s (2024) analysis of voucher specimens demonstrated that Sari and Parker (2012) had evidently molecularly sampled both <em>flavidior <\/em>and <em>nuttingi<\/em>, which were non-monophyletic and deeply diverged in their study.<\/p>\n\n\n\n<p><a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/02\/2025-A.pdf\">Proposal 2025-A-4 to NACC<\/a>, by Ju\u00e1rez et al. to recognize <em>flavidior <\/em>as specifically distinct has passed, and AviList Core Team (2025) has accepted this recommendation. It should be noted, however, that vocal differences appear to exist between <em>nuttingi <\/em>and <em>inquietus <\/em>as well, and thus their taxonomic status requires further study.<\/p>\n\n\n\n<p><strong>English names: <\/strong>For the widespread Nutting\u2019s Flycatcher <em>Myiarchus nuttingi<\/em>, the longstanding eponym that mirrors its specific epithet has been retained, while for the much more range-restricted <em>Myiarchus flavidior<\/em>, the name Salvadoran Flycatcher was chosen by NACC, as that country forms its core range, although it also occurs from southernmost Mexico to western Honduras and northernmost Nicaragua.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Tawny-crowned Greenlet <\/strong><strong><em>Tunchiornis ochraceiceps<\/em><\/strong> is split into four species<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21924 species) One of the many small Neotropical vireos known as greenlets (though they lack any green), the Tawny-crowned Greenlet is now known not only to be in a different genus, but to represent four species, mostly in Middle America and Amazonia.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 19122\u201319134<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Tawny-crowned Greenlet <em>Tunchiornis ochraceiceps<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>ochraceiceps, pallidipectus, nelsoni, bulunensis, ferrugineifrons, viridior, luteifrons, lutescens<\/em>, and <em>rubrifrons<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Ochre-crowned Greenlet <em>Tunchiornis ochraceiceps<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>ochraceiceps, pallidipectus, nelsoni, and bulunensis<\/em><\/li>\n\n\n\n<li>Rufous-fronted Greenlet <em>Tunchiornis ferrugineifrons<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>ferrugineifrons<\/em> and <em>viridior<\/em><\/li>\n<\/ul>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Guianan Greenlet <em>Tunchiornis luteifrons<\/em> (monotypic)<\/li>\n\n\n\n<li>Para Greenlet <em>Tunchiornis rubrifrons<\/em>&nbsp;<\/li>\n<\/ul>\n\n\n\n<p>subspecies <em>lutescens<\/em> and <em>rubrifrons<\/em><\/p>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/19-Tunchiornis-ochraceiceps-graphical-abstract.png\" alt=\"\" class=\"wp-image-1096 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/19-Tunchiornis-ochraceiceps-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/19-Tunchiornis-ochraceiceps-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/19-Tunchiornis-ochraceiceps-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/19-Tunchiornis-ochraceiceps-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the Neotropics showing the ranges of the four species into which Tawny- crowned Greenlet <em>Tunchiornis ochraceiceps <\/em>is partitioned. Range outlines of daughter species modified here following Buainain et al. (2021).<\/figcaption><\/figure>\n\n\n\n<p>Formerly considered just one species in the genus <em>Hylophilus<\/em>, the long-standing species construct known as Tawny-crowned Greenlet has been shown to require its own genus, which was named <em>Tunchiornis <\/em>(Slager et al. 2014, Slager and Klicka 2014). Although conservatively plumaged, four taxa that were all originally described at the species level, <em>ochraceiceps <\/em>(Sclater, 1860), <em>ferrugineifrons <\/em>(Sclater, 1862), <em>luteifrons <\/em>(Sclater, 1881), and <em>rubrifrons <\/em>(Sclater and Salvin, 1867) but were long treated as conspecific (e.g. Blake 1968, in Volume 14 of Peters\u2019 Check-list) were shown to be deeply diverged genetically, well above the level usually associated with specific distinctness (Slager et al. 2014, Buainain et al. 2021). Most of the contact zones are across major rivers, or the Andes, and require further study. Some vocal differences are evident (Boesman 2016: 168, Buainain et al. 2021), especially between Guianan Shield <em>luteifrons <\/em>and the rest, but there is inconsistency and overlap, and voice has not yet been clearly demonstrated to be diagnostic of these other deeply diverged groups. In addition to genetics and voice, it is notable that western taxa have pale irides, while eastern ones have dark irides. del Hoyo and Collar (2016) considered <em>luteifrons <\/em>to be a separate species, but on the basis of the genetic results, <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1008.htm\">a four-species treatment has been accepted by SACC<\/a> and AviList Core Team (2025).&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> While this issue is still under discussion by SACC, the tentative English names above are used to denote the daughter species, and thus these are likely to change.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Eastern Warbling Vireo <\/strong><strong><em>Vireo gilvus<\/em><\/strong> and <strong>Western Warbling Vireo <\/strong><strong><em>Vireo swainsoni<\/em><\/strong> are split from <strong>Warbling Vireo <\/strong><strong><em>Vireo gilvus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Despite looking very similar, North America\u2019s Eastern and Western Warbling Vireos know how to tell; they prefer different habitats, where they sing differently, among other differences.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 19245\u201319251<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Warbling Vireo <em>Vireo gilvus<\/em><\/li>\n\n\n\n<li>subspecies <em>gilvus, swainsoni, victoriae, brewsteri<\/em>, and <em>sympatricus<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Eastern Warbling Vireo <em>Vireo gilvus<\/em> (monotypic)<\/li>\n\n\n\n<li>Western Warbling Vireo <em>Vireo swainsoni<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>swainsoni, victoriae, brewsteri<\/em>, and <em>sympatricus<\/em><\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/20-Vireo-gilvus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1097 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/20-Vireo-gilvus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/20-Vireo-gilvus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/20-Vireo-gilvus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/20-Vireo-gilvus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of North America including Mexico showing the approximate ranges of the two species into which Warbling Vireo <em>Vireo gilvus <\/em>is partitioned. Wintering ranges of the daughter species remain poorly known, though <em>swainsoni<\/em> evidently winters farther west and north relative to <em>gilvus<\/em>.<\/figcaption><\/figure>\n\n\n\n<p>The Warbling Vireo <em>Vireo gilvus <\/em>(Vieillot, 1808) is one of eastern North America\u2019s most familiar songbirds (when heard), and is largely associated with trees at the edges of wetlands. In western North America, in contrast, taxa of the <em>swainsoni <\/em>Baird, 1858 group are more typically forest birds, occurring into the mountains, with song that differs noticeably from nominate <em>gilvus<\/em>. A large number of studies that bear on their species-level taxonomy (e.g., Voelker and Rohwer 1998, Lovell 2010, Spencer 2012, Browning 2019, Sealy et al. 2000, Slager et al. 2014, Lovell et al. 2021, Carpenter et al. 2022a, b) have been carried out over many years, and taken together they show that these very similar-looking birds differ in a great many ways that are atypical of subspecies. They are deeply diverged genetically, they hybridize rather infrequently in a zone of sympatry, they prefer different habitats, their songs differ, they have different molt schedules, and they differ in response to cowbird parasitism. They were originally described as separate species, and there are also several morphological differences on average, but these are often difficult to perceive, even in good photographs.<\/p>\n\n\n\n<p>Based on the cumulative weight of evidence, which is far greater than that available for the vast majority of such decisions, NACC (based on a proposal by Cicero 2025, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/05\/2025-C.pdf\">2025-C-3<\/a>) and AviList Core Team (2025) have voted to treat <em>gilvus <\/em>as a separate species from the <em>swainsoni <\/em>group, now a species. Further study is needed regarding the taxonomic status of the isolated taxon in the mountains of the Cape region of southern Baja California Sur, <em>victoriae <\/em>Sibley, 1940, which is larger-billed than other taxa sampled of the <em>swainsoni <\/em>group, and was eventually elevated to species status by Sibley (1996).<\/p>\n\n\n\n<p><strong>English names<\/strong>: Both taxa have long been known as Warbling Vireo, and the English names Eastern Warbling Vireo (whether hyphenated, as by NACC, or not) and Western Warbling Vireo have been used for many years in many studies, and were adopted by NACC (Chesser et al. 2025) and AviList.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Western Red-legged Thrush <\/strong><strong><em>Turdus plumbeus<\/em><\/strong> and <strong>Eastern Red-legged Thrush <\/strong><strong><em>Turdus ardosiaceus<\/em><\/strong> are split from <strong>Red-legged Thrush <\/strong><strong><em>Turdus plumbeus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) While the Bahamas and Cuba share several bird species unique to that region, Hispaniola and Puerto Rico do not, but the newly split Eastern Red-legged Thrush is very similar on the latter two islands, and (surprisingly) also occurs on far-flung Dominica.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 28619\u201328629<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Red-legged Thrush <em>Turdus plumbeus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>plumbeus, rubripes, perditus, schistaceus, coryi, ardosiaceus<\/em>, and <em>albiventris<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Western Red-legged Thrush <em>Turdus plumbeus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>plumbeus, rubripes, perditus, schistaceus<\/em>, and <em>coryi<\/em><\/li>\n\n\n\n<li>Eastern Red-legged Thrush <em>Turdus ardosiaceus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>ardosiaceus<\/em> and <em>albiventris<\/em><\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/21-Turdus-plumbeus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1098 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/21-Turdus-plumbeus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/21-Turdus-plumbeus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/21-Turdus-plumbeus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/21-Turdus-plumbeus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the West Indies showing the approximate ranges of the two species into which Red-legged Thrush <em>Turdus plumbeus<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>The Red-legged Thrush <em>Turdus plumbeus<\/em> Linnaeus, 1758 has long been treated as comprised of about six widely distributed Caribbean taxa (as in Ripley 1964, in Volume 10 of Peters\u2019 Check-list). Those from the islands of Hispaniola, Puerto Rico, and Dominica, which form the <em>ardosiaceus <\/em>Vieillot, 1822 group, however, were originally described as a separate species, and continued to be treated as separate species by Hellmayr (1934). Ridgway (1907) had treated them as constituting three species, the third being <em>rubripes<\/em> Temminck, 1826 of Cuba and Cayman Brac, and this three-way treatment was recently espoused by del Hoyo and Collar (2016), on the basis of plumage, and for <em>ardosiaceus<\/em>, song characteristics (Boesman 2016: 310). In addition, relatively deep genetic divergences separate these two groups (Nylander et al. 2008, Batista et al. 2020).&nbsp;<\/p>\n\n\n\n<p>Although there are plumage and bill color differences between Bahamian nominate <em>plumbeus <\/em>and the other taxa in the <em>rubripes <\/em>group, and there may be song differences as well, these are not as pronounced as the differences between the <em>ardosiaceus <\/em>group and the remaining taxa, and the degree of genetic divergence between these groups is evidently not known. In addition, the plumage of <em>schistaceus <\/em>of eastern Cuba [and that of Cayman Brac <em>coryi<\/em> (Sharpe, 1902) and the extinct Swan Islands <em>perdita<\/em> Kirwan &amp; Collar, 2023 (a replacement name for <em>Mimocichla rubripes eremita <\/em>Ridgway, 1905)] can be interpreted as intermediate between that of Bahamian <em>plumbeus <\/em>and western Cuban <em>rubripes<\/em>. Thus, the decision by AviList Core Team (2025) was to enact the two-way split of the more diverged taxa from Hispaniola to Dominica, the <em>ardosiaceus <\/em>group. However, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2022\/04\/2022-A-final.pdf\">Proposal 2022-A-03 to NACC<\/a> (Remsen 2022) to split <em>Turdus plumbeus <\/em>did not pass due partly to the lack of a published vocal analysis, and scepticism over the specific value of plumage characters in thrushes.<\/p>\n\n\n\n<p>Controversy exists over the subspecific validity of the Dominican population named <em>albiventris <\/em>(Sclater, 1889), as it was postulated to be the result of pre-Columbian human introduction. However, as Allen (1891) showed when he described it as <em>Mimocichla verrillorum <\/em>(evidently being unaware of Sclater\u2019s description two years earlier), it has several distinct physical characteristics such as smaller size and especially small bill and wings, greater extent of white on the belly, and more white in the tail, traits that do not seem commensurate with evolution in isolation over such a short period of time as would be the case if human-mediated. These traits were reevaluated and largely confirmed by S.L. Olson in Olson and Ricklefs (2009). In Olson\u2019s opinion, <em>albiventris <\/em>is such a well-marked subspecies as to make the human introduction hypothesis unlikely. Likewise, Kirwan and Collar (2023) have recently shown that both <em>perdita<\/em>, formerly of Swan Islands, and <em>coryi <\/em>of Cayman Brac are likely diagnosable (but sample sizes are small), rather than being consubspecific with western Cuban <em>rubripes<\/em>.<\/p>\n\n\n\n<p><strong>English names:<\/strong> Given their distributions and the entrenched nature of the name Red-legged Thrush, the names Western Red-legged Thrush for <em>plumbeus s.s<\/em>. and Eastern Red-legged Thrush for <em>ardosiaceus <\/em>have been tentatively adopted. The concept of the name Western Red-legged Thrush differs from that used by del Hoyo and Collar (2016), however, as they adopted a three-way split and used Western to refer to their <em>rubripes <\/em>species, and further discussion is needed.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Dagua Thrush <\/strong><strong><em>Turdus daguae<\/em><\/strong> is split from <strong>White-throated Thrush <\/strong><strong><em>Turdus assimilis<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Another Choc\u00f3 endemic, the Dagua Thrush, makes its debut as a split from the widespread Mesoamerican White-throated Thrush.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 28724\u201328734<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>White-throated Thrush <em>Turdus assimilis<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>calliphthongus, lygrus, assimilis, leucauchen, rubicundus, atrotinctus, cnephosus, coibensis<\/em>, and <em>daguae<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>White-throated Thrush <em>Turdus assimilis<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>suttoni, calliphthongus, lygrus, assimilis, leucauchen, rubicundus, atrotinctus, cnephosus<\/em>, and <em>coibensis<\/em><\/li>\n\n\n\n<li>Dagua Thrush <em>Turdus daguae<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/22-Turdus-assimilis-graphical-abstract.png\" alt=\"\" class=\"wp-image-1099 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/22-Turdus-assimilis-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/22-Turdus-assimilis-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/22-Turdus-assimilis-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/22-Turdus-assimilis-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of the northern Neotropics showing the ranges of the two species into which White-throated Thrush <em>Turdus assimilis <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>The taxonomy of New World members of the cosmopolitan thrush genus <em>Turdus <\/em>is highly complex, and has undergone considerable recent change (with more sure to follow), the <em>Turdus assimilis<\/em> Cabanis, 1851 complex being no exception. Ripley (1964, in the tenth volume of Peters\u2019 Check-list) considered all the mainly Mesoamerican taxa of <em>assimilis <\/em>(including <em>daguae<\/em>) to be conspecific with South American <em>Turdus albicollis<\/em> Vieillot, 1818. Most recent authors have considered <em>assimilis <\/em>and <em>albicollis <\/em>to be separate species, but Collar (2005) again treated all as a single species, while del Hoyo and Collar (2016) treated <em>daguae <\/em>as a subspecies of <em>albicollis <\/em>rather than <em>assimilis<\/em>, and Ridgely and Greenfield (2001) treated <em>daguae <\/em>as a full species (summarized in Remsen 2021; <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2022\/04\/2022-A-final.pdf\">NACC proposal set 2022-A<\/a>).<\/p>\n\n\n\n<p>Recent work has underscored the distinctiveness of form <em>daguae<\/em> Berlepsch, 1897 of far southern Panama to southwestern Ecuador, which was originally described as a species. An initial proposal to NACC, Proposal 2022-A-4, <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop922.htm\">and to SACC<\/a>, both failed. However, <em>daguae <\/em>is distinctive in plumage and size (N\u00fa\u00f1ez-Zapata et al. 2016), voice (Boesman 2016: 305), and genetics (N\u00fa\u00f1ez-Zapata et al. 2016), and a follow-up proposal (Johnson and Cooper 2025), <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2025\/05\/2025-C.pdf\">Proposal 2025-C-12 to NACC<\/a>, led to it being considered a full species by NACC (Chesser et al. 2025); furthermore, it has <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1047.htm\">passed a reconsideration by SACC<\/a>, and is accorded full species status by AviList Core Team (2025). A further issue in the SACC proposal regarding the split of the <em>phaeopygus <\/em>group is also under consideration, as well as by AviList. See also Subspecies Changes for the resurrection of <em>suttoni<\/em>. The remaining taxa are divisible into at least two groups, the <em>assimilis <\/em>and <em>leucauchen <\/em>groups (Howell and Webb 1995).<\/p>\n\n\n\n<p><strong>English names:<\/strong> The name Dagua Thrush refers to the type locality, the R\u00edo Dagua in Colombia. While this by no means encompasses the entirety of the species\u2019 range, it has been used extensively both as a species and group name, and with no obvious competing English names, is adopted by NACC and thus here.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Yellow-mandibled Sparrow <\/strong><strong><em>Arremon axillaris<\/em><\/strong> is split from <strong>Pectoral Sparrow <\/strong><strong><em>Arremon taciturnus<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The smartly attired Yellow-mandibled Sparrow is now recognized as an endemic to the base of the northern Andes, separate from the mostly Amazonian Pectoral Sparrow.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 33068\u201333071<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pectoral Sparrow <em>Arremon taciturnus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>taciturnus, nigrirostris<\/em>, and <em>axillaris<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pectoral Sparrow <em>Arremon taciturnus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>taciturnus<\/em> and <em>nigrirostris<\/em><\/li>\n\n\n\n<li>Yellow-mandibled Sparrow <em>Arremon axillaris<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/23-Arremon-taciturnus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1100 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/23-Arremon-taciturnus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/23-Arremon-taciturnus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/23-Arremon-taciturnus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/23-Arremon-taciturnus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the two species into which Pectoral Sparrow <em>Arremon taciturnus <\/em>is partitioned. Range outlines modified largely based on Buainain et al. (2017), supplemented by Hilty (2021), Schulenberg et al. (2007), and Herzog et al. (2019).<\/figcaption><\/figure>\n\n\n\n<p>Initially described as a species, the yellow-billed taxon <em>axillaris <\/em>Sclater, 1855 of the foothills region of central Colombia and southwestern Venezuela was long considered a subspecies of the mainly Amazonian <em>Arremon taciturnus<\/em> Hermann, 1783. Paynter (1970, in Volume 13 of Peters\u2019 Check-list), included not only <em>axillaris <\/em>but also southeastern Brazilian <em>semitorquatus <\/em>Swainson, 1838 in <em>taciturnus<\/em>. Much later <em>franciscanus <\/em>Raposo, 1997 was described from interior Minas Gerais and Bahia, and both it and <em>semitorquatus <\/em>are now considered distinct species.&nbsp;<\/p>\n\n\n\n<p>Specific status was accorded to <em>axillaris <\/em>by del Hoyo and Collar (2016) on the basis of morphological and song differences (Boesman 2016: 361), and shortly thereafter Buainain et al. (2017) published a detailed integrative analysis of the complex, followed later by genetic analysis in Buainain et al. (2022) that showed relatively deep divergence, of a degree more typically associated with species-level taxa than with subspecies. Although the vocal differences require further study, <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1011.htm\">on the basis of these analyses SACC<\/a> and AviList Core Team (2025) now recognize <em>axillaris <\/em>as a distinct species.<\/p>\n\n\n\n<p><strong>English names:<\/strong> Given the huge range of Pectoral Sparrow and the familiarity of its English name, there seems no reason to change its English name, while the name Yellow-mandibled Sparrow adequately describes its most obvious morphological difference and has gained some familiarity, so has been adopted by SACC and thus here.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Gray-crowned Ground-Sparrow <\/strong><strong><em>Melozone occipitalis<\/em><\/strong> is split from <strong>White-eared Ground-Sparrow <\/strong><strong><em>Melozone leucotis<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Another Middle American endemic species is now recognized, with the split of Gray-crowned Ground-Sparrow of southern Mexico and northern Central America.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 33357\u201333360<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>White-eared Ground-Sparrow <em>Melozone leucotis<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>occipitalis, nigrior<\/em>, and <em>leucotis<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>White-eared Ground-Sparrow <em>Melozone leucotis<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>nigrior<\/em> and <em>leucotis<\/em><\/li>\n\n\n\n<li>Gray-crowned Ground-Sparrow <em>Melozone occipitalis<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/24-Melozone-leucotis-graphical-abstract.png\" alt=\"\" class=\"wp-image-1101 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/24-Melozone-leucotis-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/24-Melozone-leucotis-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/24-Melozone-leucotis-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/24-Melozone-leucotis-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of Mexico and Central America showing the ranges of the two species into which White-eared Ground-Sparrow <em>Melozone leucotis <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Three taxa have long been treated as conspecific under <em>Melozone leucotis<\/em> Cabanis, 1861, with <em>nigrior<\/em> Miller &amp; Griscom, 1925, occurring locally in central Honduras and northern Nicaragua, <em>occipitalis <\/em>(Salvin, 1878) of southeastern Chiapas to western El Salvador, and the nominate restricted to the Guanacaste Cordillera, on the Pacific slope of northwestern Costa Rica. Of these, <em>occipitalis <\/em>was originally described as a species, while <em>nigrior <\/em>was described later as a subspecies of <em>leucotis<\/em>; notably, these authors (Miller and Griscom 1925) continued to recognize <em>occipitalis <\/em>as a full species. Much later, del Hoyo and Collar (2016) also treated <em>occipitalis <\/em>at the species level.<\/p>\n\n\n\n<p>Sandoval and colleagues recently published a series of papers on bioacoustics of the <em>Melozone leucotis <\/em>complex (e.g., Sandoval et al. 2016, 2017). Sandoval et al. (2017) further examined morphological and genetic divergence in the complex, and their findings resulted in the decision by AviList Core Team (2025) to split <em>occipitalis <\/em>as a full species. A follow-up proposal to NACC (Billerman 2023; <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2023\/08\/2023-C.pdf\">2023-C-12<\/a>) to split <em>occipitalis<\/em>, however, did not pass, with some voters perceiving the differences as being at the level of subspecies rather than species.&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> As used by del Hoyo and Collar (2016), the English name White-eared Ground-Sparrow is tentatively retained for <em>Melozone leucotis<\/em>, although it is the species with the smaller range, while Gray-crowned Ground-Sparrow, used (as Grey-crowned by del Hoyo and Collar 2016) is tentatively adopted for <em>Melozone occipitalis<\/em>. Given that the crown color of <em>occipitalis <\/em>is not very pronounced, and that both have equally white auriculars, perhaps other English names would be more suitable.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Black-fronted Brushfinch <\/strong><strong><em>Atlapetes nigrifrons<\/em><\/strong> is split from <strong>Yellow-breasted Brushfinch <\/strong><strong><em>Atlapetes latinuchus<\/em><\/strong>&nbsp;<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The brushfinch that frequents feeders in the Perij\u00e1 Mountains of the Colombia-Venezuela border turns out not to be a Yellow-breasted Brushfinch after all, and is now considered a separate species, Black-fronted Brushfinch.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 33484\u201333494<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Yellow-breasted Brushfinch <em>Atlapetes latinuchus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>elaeoprorus, caucae, spodionotus, comptus, latinuchus, chugurensis, baroni, yariguierum<\/em>, and <em>nigrifrons<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Yellow-breasted Brushfinch <em>Atlapetes latinuchus<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>elaeoprorus, caucae, spodionotus, comptus, latinuchus, chugurensis, baroni<\/em>, and <em>yariguierum<\/em><\/li>\n\n\n\n<li>Black-fronted Brushfinch <em>Atlapetes nigrifrons<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/25-Atlapetes-latinuchus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1102 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/25-Atlapetes-latinuchus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/25-Atlapetes-latinuchus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/25-Atlapetes-latinuchus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/25-Atlapetes-latinuchus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of northern South America showing the ranges of the two species into which Yellow-breasted Brushfinch <em>Atlapetes latinuchus <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>The <em>Atlapetes latinuchus<\/em> (Du Bus de Gisignies, 1855) complex, distributed in several subspecies from the Venezuela\/Colombia border southward in the Andes to central Peru, was formerly included within the larger species <em>Atlapetes rufinucha<\/em> (d&#8217;Orbigny &amp; de Lafresnaye, 1837) (as by Paynter 1970, in Volume 13 of Peters\u2019 Check-list). The northernmost form, from the Perij\u00e1 Mountains, was described relatively late, as <em>Atlapetes rufinucha nigrifrons <\/em>Phelps &amp; Gilliard, 1940. Significantly, Phelps and Gilliard (1940) stated \u201c[t]his new subspecies is not closely allied to any particular race of <em>A. rufinucha<\/em>. Its broad, solid black forehead distinguishes it from all others.\u201d<\/p>\n\n\n\n<p>Garc\u00eda-Moreno and Fjelds\u00e5 (1999) showed in an early mtDNA paper that <em>rufinucha <\/em>and the <em>latinuchus <\/em>complex are non-sister, a result that has more recently been strongly corroborated (S\u00e1nchez-Gonz\u00e1lez et al. 2015), leading to the treatment of <em>latinuchus <\/em>as an independent, still highly polytypic species. Within the genus <em>Atlapetes <\/em>as then constituted, <em>nigrifrons <\/em>was found to be preoccupied by <em>Atlapetes torquatus nigrifrons <\/em>(Chapman, 1923), and the name was replaced by <em>Atlapetes latinuchus phelpsi <\/em>Paynter, 1970. However, with the more recent move of the <em>torquatus <\/em>clade to <em>Arremon<\/em>, there remains no need for Paynter\u2019s replacement name, and <em>nigrifrons <\/em>is again the name in force for the Perij\u00e1 form under discussion here (Donegan 2006, <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop222.htm\">SACC proposal 222<\/a>).&nbsp;<\/p>\n\n\n\n<p>Donegan and Huertas (2006) suggested, on the basis of a phylogeny using plumage characters, that <em>nigrifrons <\/em>was misplaced in the <em>latinuchus <\/em>complex and belongs in a clade with <em>Atlapetes melanocephalus<\/em> (Salvin &amp; Godman, 1880) of the Santa Marta range and the intermediate \u201cPerij\u00e1 bird\u201d; however, plumage characters may carry misleading phylogenetic signal in this group. An in-depth study including a vocal analysis by Donegan et al. (2014) further confirmed that <em>nigrifrons <\/em>is much more vocally similar to <em>melanocephalus <\/em>and <em>albofrenatus <\/em>than any of these are to <em>Atlapetes latinuchus<\/em>.&nbsp; Unpublished phylogenetic data (by D. Cadena) are said to confirm that <em>nigrifrons <\/em>is not sister to <em>latinuchus<\/em>. As suggested by Donegan et al. (2014), it may be more closely related to <em>Atlapetes albofrenatus<\/em> (Boissonneau, 1840), although genetic data are lacking. In addition, some rather intermediate-looking specimens (called the \u201cPerij\u00e1 bird\u201d) are known that may indicate introgression between <em>nigrifrons <\/em>and <em>albofrenatus<\/em>, or they may be an undescribed subspecies of <em>albofrenatus<\/em>. The latter suggestion received support from the observation of non-intermediacy of mantle color differences and apparent elevational replacement, with <em>nigrifrons <\/em>occurring at higher elevations.&nbsp;<\/p>\n\n\n\n<p>On the basis of the above, del Hoyo and Collar (2016) considered <em>nigrifrons <\/em>a separate species. An earlier <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop222.htm\">proposal to SACC to split <em>nigrifrons<\/em><\/a><em> <\/em>(Donegan), did not pass and was eventually withdrawn. As <em>nigrifrons <\/em>is clearly not correctly assigned to <em>latinuchus<\/em>, it is tentatively accorded species status by AviList Core Team (2025), although further work may show it is better considered a subspecies of <em>albofrenatus<\/em>.<\/p>\n\n\n\n<p><strong>English names:<\/strong> As used by del Hoyo and Collar (2016), Yellow-breasted Brushfinch is tentatively retained for the widespread, polytypic species <em>Atlapetes latinuchus s.s.<\/em>, while Black-fronted Brushfinch is used for <em>Atlapetes nigrifrons<\/em>. The latter name is apt, highlighting the taxon\u2019s most distinctive feature, especially given that the name Perija Brushfinch is not available, being already in wide use for <em>Arremon perijanus<\/em>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Northern Yellow Warbler <\/strong><strong><em>Setophaga aestiva<\/em><\/strong> and <strong>Mangrove Yellow Warbler <\/strong><strong><em>Setophaga petechia<\/em><\/strong> are split from <strong>Yellow Warbler <\/strong><strong><em>Setophaga petechia<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species)&nbsp; With the two-way split of Yellow Warbler, birders in Neotropical mangroves will need to carefully document the warblers they are likely to encounter there.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 34087\u201334130<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Yellow Warbler <em>Setophaga petechia<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>rubiginosa, amnicola, aestiva, morcomi, sonorana, dugesi, oraria, bryanti, erithachorides, chrysendeta, paraguanae, cienagae, castaneiceps, rhizophorae, xanthotera, aequatorialis, peruviana, aureola, rufivertex, armouri, flavida, eoa, gundlachi, albicollis, cruciana, bartholemica, melanoptera, ruficapilla, babad, petechia, alsiosa, rufopileata, obscura<\/em>, and <em>aurifrons<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Northern Yellow Warbler <em>Setophaga aestiva<\/em><\/li>\n\n\n\n<li>subspecies <em>rubiginosa, amnicola, aestiva, morcomi, sonorana<\/em>, and <em>dugesi<\/em><\/li>\n\n\n\n<li>Mangrove Yellow Warbler <em>Setophaga petechia<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>oraria, bryanti, erithachorides, chrysendeta, paraguanae, cienagae, castaneiceps, rhizophorae, xanthotera, aequatorialis, peruviana, aureola, rufivertex, armouri, flavida, eoa, gundlachi, albicollis, cruciana, bartholemica, melanoptera, ruficapilla, babad, petechia, alsiosa, rufopileata, obscura<\/em>, and <em>aurifrons<\/em><\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/26-Setophaga-petechia-graphical-abstract.png\" alt=\"\" class=\"wp-image-1103 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/26-Setophaga-petechia-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/26-Setophaga-petechia-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/26-Setophaga-petechia-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/26-Setophaga-petechia-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of North to northern South America  showing the approximate ranges of the two species into which Yellow Warbler <em>Setophaga petechia<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>A comprehensive proposal (Browning 2018, <a href=\"https:\/\/americanornithology.org\/wp-content\/uploads\/2020\/02\/2018-C-amended.pdf\">Proposal 2018-C-2<\/a> to NACC), which did not pass, forms the basis for much of the following summary; in turn, much of that proposal is based on Browning (1994). The sheer number of taxa and geographic distances involved have defeated most attempts to gain an understanding of the taxonomy of the Yellow Warbler complex. However, a selection of the many studies impinging on this matter are briefly discussed below.&nbsp;<\/p>\n\n\n\n<p>Long treated as at least two species, the many taxa of Yellow Warbler <em>Setophaga petechia<\/em> (Linnaeus, 1766) (of which 12 that are currently recognized in AviList v2025 were originally described as full species) were united by AOU (1945). This followed the convincing demonstration by Aldrich (1942) of gradients between characters supposedly diagnostic of the tropical <em>petechia <\/em>group vs. the north-temperate-breeding <em>aestiva <\/em>(Gmelin, 1789) group.&nbsp;<\/p>\n\n\n\n<p>Although they are broadly allopatric in the US, ranges of apparently resident taxa of both groups are in close proximity in west-central Mexico, albeit strongly segregated by habitat (upland for <em>aestiva <\/em>group vs. mangroves for the broad-sense <em>petechia <\/em>group, here used to indicate all sedentary coastal subtropical to tropical taxa). They are also very commonly in contact in the nonbreeding season through much of the range of the <em>petechia <\/em>group, including in mangroves, where the <em>aestiva <\/em>group commonly winters. The single-species treatment was maintained by Lowery and Monroe (1968, in Volume 14 of Peters Check-list), although not adhered to by all (e.g. Ridgely 1976, who treated <em>erithachorides <\/em>and <em>petechia <\/em>as separate species).&nbsp;<\/p>\n\n\n\n<p>An early mtDNA phylogeny (Klein and Brown 1994) found deep divergence between the temperate zone-breeding <em>aestiva <\/em>group which breeds mostly in wooded riparian habitats, especially willows, and the subtropical- to tropical-breeding, mostly mangrove-inhabiting broad <em>petechia <\/em>group, including the <em>erithachorides <\/em>group (Baird, 1858). Although Klein and Brown (1994) did not consider their results to demonstrate that more than one species is involved, they were interpreted by Ridgely and Greenfield (2001) as supporting at least a two-species treatment, and in this Ridgely and Greenfield were followed by IOC (from version 2.1 onward). In addition, Hilty (2003) treated both <em>petechia s.s. <\/em>and <em>erithachorides <\/em>as separate species, citing two genetic studies.<\/p>\n\n\n\n<p>Wiedenfeld (1991) showed that the inclusive <em>Dendroica petechia s.l.<\/em> does not follow either Bergmann\u2019s or Allen\u2019s rules, with most tropical populations being larger overall than temperate-breeding ones. However, wing length varied with latitude, as earlier shown by Aldrich (1942).<\/p>\n\n\n\n<p>Mennill (2001) found that \u201cMangrove Warblers\u201d from the Yucatan Peninsula had significantly lower-pitched songs that were also longer and with different syllabic composition than songs of Northern Yellow Warbler. Mennill (2001) also noted that both sexes of the members of the <em>petechia <\/em>group sing and defend territories year-round, unlike the <em>aestiva <\/em>group, in which only males sing and defend territories, and they only sing seasonally. However, playback often elicits strong responses from the \u201cwrong\u201d taxa, but given that this happens sometimes between universally recognized species, its significance is unclear.<\/p>\n\n\n\n<p>The typical call note (termed a \u201cbark\u201d) given by the <em>aestiva <\/em>group has long been known to be a sharp <em>chip!<\/em>, while that of the <em>petechia <\/em>group is a soft <em>chup<\/em> (Morton and Stutchbury 1991). The now-extensive publicly available sound archives allow for easy rangewide confirmation of this obvious call note difference on a large scale (P.C. Rasmussen, pers. obs.).&nbsp;<\/p>\n\n\n\n<p>The early yet remarkably comprehensive phylogenetic study based on mtDNA of Klein and Brown (1994), showed relatively deep divergence between the <em>aestiva <\/em>and broad <em>petechia <\/em>groups. In a subsequent mtDNA phylogeny of parulid warblers, Lovette and Bermingham (1999) found higher divergence levels within the inclusive <em>Setophaga petechia <\/em>complex than for other parulid warbler species.<\/p>\n\n\n\n<p>A study of genetic variation among Galapagos populations found little structure among islands, but fairly deep divergence between Galapagos and the continental populations sampled (Browne et al. 2008). Another study (Chaves et al. 2012) found that Cocos and Galapagos populations were fairly recently diverged, probably from a Central American colonization.&nbsp;<\/p>\n\n\n\n<p>An unusual situation has been documented on Cozumel Island (Machkour-M\u2019Rabet et al. 2023), in which the resident <em>rufivertex <\/em>(Ridgway, 1885), which breeds in uplands, is supplanted in mangroves by what the authors considered a new form that shows intermediacy in song, morphology, and genetics with adjacent mainland <em>bryanti <\/em>(Ridgway, 1873). A similar, though less well-documented, example of apparent abrupt intergradation between dissimilar taxa occurs on the Paraguana Peninsula of northern Venezuela (see Graphical Abstract under the Changes to Groups section).&nbsp;<\/p>\n\n\n\n<p>Salgado-Ortiz et al. (2008) found the breeding ecology of the population of Mangrove Warbler (<em>bryanti<\/em>) they studied on the western Yucatan Peninsula to differ strongly from that in numerous published studies of temperate Yellow Warblers, specifically in the longer breeding season, smaller clutches, extended incubation and nestling periods, lowered nesting success, higher nest predation, and higher annual adult survival of <em>bryanti<\/em>.&nbsp;<\/p>\n\n\n\n<p>A <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop62.htm\">2003 proposal to SACC<\/a> to split <em>aestiva <\/em>and <em>petechia<\/em>, failed, as have two proposals to NACC (in 2004 and 2018). Nevertheless, at the very least, it is certain that the <em>aestiva <\/em>and (broad) <em>petechia <\/em>groups are much more divergent in multiple aspects, especially genetic and ecological ones, than is any other parulid warbler species normally treated as a single species. The evidence for any further splits within the broad <em>petechia <\/em>group, however, is far less clear and compelling. Thus, <em>petechia <\/em>and <em>aestiva <\/em>are now considered full species by AviList Core Team (2025) based on their strong divergence in multiple ways.&nbsp;<\/p>\n\n\n\n<p><strong>English names:<\/strong> Given the extreme familiarity of the name Yellow Warbler <em>Setophaga petechia<\/em>, it is considered inadvisable to retain this for just one of the daughter species because of the massive confusion that would cause. Both American Yellow Warbler and Northern Yellow Warbler have been used extensively to refer to <em>Setophaga aestiva s.s<\/em>., but Northern Yellow Warbler is tentatively used here because all taxa in the complex are equally American in distribution, while only <em>aestiva s.s.<\/em> is northern-breeding. It is considered important to retain the group name \u201cYellow\u201d due to its familiarity, and with the expectation that most people will continue to informally refer to them as Yellow Warbler. The name Mangrove Warbler is also considered too potentially confusing for <em>petechia s.s., <\/em>when including the <em>erithachorides <\/em>group, long known as the Mangrove Warbler, but to the exclusion of the \u201cGolden Warbler\u201d <em>S. petechia <\/em>and, in some cases such as Clements, the Galapagos <em>aureola <\/em>group. However, most forms of <em>petechia s.s.<\/em> occur primarily or exclusively in mangroves, where they are often among the most abundant and conspicuous birds of that biotope. To preserve the indication of group membership, and to emphasize their characteristic habitat, the name Mangrove Yellow Warbler is tentatively adopted, bearing in mind that it may eventually be hyphenated as Yellow-Warbler, or otherwise changed.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Rose-bellied Chat <\/strong><strong><em>Granatellus paraensis<\/em><\/strong> is split from <strong>Rose-breasted Chat <\/strong><strong><em>Granatellus pelzelni<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The <em>Granatellus <\/em>chat occurring east of the Tocantins River in east-central Brazil differs strongly in most of its vocalizations and in DNA, and thus is considered a separate species.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 34571\u201334572<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Rose-breasted Chat <em>Granatellus pelzelni<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>pelzelni<\/em> and <em>paraensis<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Rose-breasted Chat <em>Granatellus pelzelni<\/em> (monotypic)<\/li>\n\n\n\n<li>Rose-bellied Chat <em>Granatellus paraensis<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/27-Granatellus-pelzelni-graphical-abstract.png\" alt=\"\" class=\"wp-image-1104 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/27-Granatellus-pelzelni-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/27-Granatellus-pelzelni-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/27-Granatellus-pelzelni-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/27-Granatellus-pelzelni-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the two species into which Rose-breasted Chat <em>Granatellus pelzelni <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Although morphological differentiation is fairly slight between all species of the widely distributed Neotropical genus <em>Granatellus<\/em>, the taxa on either side of the Tocantins River of eastern Brazil differ rather abruptly, though subtly. This contrasts with the lack of morphological differentiation across the wide range of <em>pelzelni <\/em>Sclater, 1865, including where it crosses major rivers, even the Amazon, which forms a barrier for so many other species. Yet, on the east side of the Tocantins, <em>paraensis <\/em>Rothschild, 1906, which even Rothschild described as a subspecies, exhibits moderate plumage differences, though these could well be considered subspecific. Long treated as conspecific with <em>pelzelni<\/em>, including by Lowery and Monroe (1968, in Volume 14 of Peters Check-list), <em>paraensis <\/em>was considered by del Hoyo and Collar (2016) to be a distinct species, largely on the basis of Boesman (2016: 384), who found (based on a very small sample) remarkable vocal differentiation. Subsequently, Dornas et al. (2022) found that <em>paraensis <\/em>and <em>pelzelni <\/em>are relatively deeply diverged from each other, thus strengthening the case of specific separation of <em>paraensis<\/em>.&nbsp; Furthermore, newly available recordings largely bolster the case as well, though not without creating further uncertainty (as in <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1019.htm\">this SACC proposal<\/a>, in which the split failed). Boesman (2016: 384) commented that, while the \u201cjrt\u201d call note is typically given by <em>pelzelni<\/em>, it has not been recorded for <em>paraensis. <\/em>This call of <em>pelzelni<\/em> is seemingly invariable over large areas; the below map shows localities of ML and xeno-canto recordings (many more than were available to Boesman) of the distinctive and frequently given \u201cjrt\u201d call note (often for long periods, as in the recording below). Notably, none are from east of the Tocantins, in the range of <em>paraensis<\/em>.<\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1006\" height=\"842\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/map-spectrogram-granatellus-paraensis.jpg\" alt=\"\" class=\"wp-image-1266 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/map-spectrogram-granatellus-paraensis.jpg 1006w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/map-spectrogram-granatellus-paraensis-720x603.jpg 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/map-spectrogram-granatellus-paraensis-768x643.jpg 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/map-spectrogram-granatellus-paraensis-480x402.jpg 480w\" data-sizes=\"(max-width: 1006px) 100vw, 1006px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1006px; --smush-placeholder-aspect-ratio: 1006\/842;\" \/><figcaption class=\"wp-element-caption\">Map of northern South America showing localities of Macaulay Library and xeno-canto recordings of the call of Rose-breasted Chat <em>Granatellus pelzelni<\/em>. The blue arrow indicates the location of the recording in the spectrogram above. <a href=\"https:\/\/macaulaylibrary.org\/asset\/380127601\">Listen to this recording<\/a>.<\/figcaption><\/figure>\n\n\n\n<p>Additionally, mapping songs of <em>pelzelni <\/em>showed that, while somewhat variable, across major barriers and huge distances they are all comprised of the same type of simple, repeated series, unlike most songs thus far known for <em>paraensis<\/em>, which are complex and quite distinct. Further study is needed to understand vocal variation and potentially female song in <em>paraensis<\/em> (<a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1019.htm\">see SACC proposal<\/a>), but a reconsideration of the matter by AviList in 2025 affirmed the decision to split <em>paraensis<\/em>.<\/p>\n\n\n\n<p><strong>English names:<\/strong> The English names adopted by del Hoyo and Collar (2016) are tentatively used here. The name of the widespread Rose-breasted Chat <em>Granatellus pelzelni<\/em> does not change, while Rose-bellied Chat is used for the range-restricted <em>Granatellus paraensis<\/em>. However, we consider that the latter is unmemorable and confusing, and it may well be replaced by a more suitable name in future.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Buff-breasted Mountain Tanager <\/strong><strong><em>Dubusia taeniata<\/em><\/strong> is split into three species<\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21923 species) While clearly closely related, three mountain tanagers, one from the endemic-rich Santa Marta region, and the other two Andean forms separated by the well-known biogeographic barrier formed by the Mara\u00f1\u00f3n Valley, are now recognized as separate species.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 34901\u201334903<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Buff-breasted Mountain Tanager <em>Dubusia taeniata<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>carrikeri, taeniata<\/em>, and <em>stictocephala<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Carriker\u2019s Mountain Tanager <em>Dubusia carrikeri<\/em> (monotypic)<\/li>\n\n\n\n<li>Buff-banded Mountain Tanager <em>Dubusia taeniata<\/em> (monotypic)<\/li>\n\n\n\n<li>Streak-crowned Mountain Tanager <em>Dubusia stictocephala<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/28-Dubusia-taeniata-graphical-abstract.png\" alt=\"\" class=\"wp-image-1105 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/28-Dubusia-taeniata-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/28-Dubusia-taeniata-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/28-Dubusia-taeniata-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/28-Dubusia-taeniata-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the three species into which Buff-breasted Mountain Tanager <em>Dubusia taeniata<\/em> is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Three allopatric taxa of mountain tanagers were originally each described as species: <em>taeniata <\/em>(Boissonneau, 1840), widespread in the northern Andes from southwestern Venezuela to far northern Peru; <em>carrikeri <\/em>Wetmore, 1946, of the Santa Marta range; and <em>stictocephala <\/em>Berlepsch &amp; Sztolcman, 1894, of the Peruvian Andes from Amazonas to Cusco. They were long considered conspecific, first when Hellmayr (1936) lumped <em>stictocephalus <\/em>with <em>taeniata<\/em>, and then when Meyer de Schauensee (1966) further lumped the later-described <em>carrikeri <\/em>with these. Storer (1970, in Volume 13 of Peters\u2019 Check-list) retained them as a single species, as did all subsequent authors until recently.&nbsp;<\/p>\n\n\n\n<p>A <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop392.htm\">proposal for a split that summarized vocal differences<\/a> between the three (Robbins et al. 2009) did not pass, largely due to the unpublished nature of the observations. Later, on the basis of plumage and song differences (Boesman 2016: 403), del Hoyo and Collar (2016) elevated all three to species status. This treatment has now been accepted by AviList Core Team (2025) and by SACC, on the basis of <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1017.htm\">a subsequent proposal<\/a> using publicly available recordings.<\/p>\n\n\n\n<p><strong>English names:<\/strong> As used by del Hoyo and Collar (2016), the English names Carriker\u2019s Mountain Tanager for <em>Dubusia carrikeri<\/em>, Buff-banded Mountain Tanager for <em>Dubusia taeniata<\/em>, and Streak-crowned Mountain Tanager for <em>Dubusia stictocephala<\/em> were adopted <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1037.htm\">after considerable discussion by SACC<\/a>, and thus here.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Black-hooded Tanager <\/strong><strong><em>Stilpnia whitelyi<\/em><\/strong> is split from <strong>Black-headed Tanager <\/strong><strong><em>Stilpnia cyanoptera<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Another tepui-region endemic, the Black-hooded Tanager, is split from Black-headed Tanger of the northern South American hills.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 34994\u201334995<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Black-headed Tanager <em>Stilpnia cyanoptera<\/em><\/li>\n\n\n\n<li>subspecies <em>cyanoptera<\/em> and <em>whitelyi<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Black-headed Tanager <em>Stilpnia cyanoptera<\/em> (monotypic)&nbsp;<\/li>\n\n\n\n<li>Black-hooded Tanager <em>Stilpnia whitelyi<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/29-Stilpnia-melanocephalus-graphical-abstract.png\" alt=\"\" class=\"wp-image-1106 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/29-Stilpnia-melanocephalus-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/29-Stilpnia-melanocephalus-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/29-Stilpnia-melanocephalus-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/29-Stilpnia-melanocephalus-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of northern South America showing the ranges of the two species into which Black-hooded Tanager <em>Stilpnia cyanoptera <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Two range-restricted tanager species of the mountains of Venezuela and adjacent countries, <em>Stilpnia c. cyanoptera <\/em>(Swainson, 1834) of the Santa Marta region eastward in coastal mountains of Venezuela, and <em>whitelyi <\/em>(Salvin &amp; Godman, 1884) of the tepui region of southern Venezuela, far northern Brazil, and western Guyana, were each originally described as species, but were lumped at least by 1936 (Hellmayr 1936:174), and followed by Storer (1970, in Volume 13 of Peters\u2019 Check-list) and thus most other authors. Since then, it has been repeatedly suggested that <em>whitelyi <\/em>might be best treated as specifically distinct (Ridgely and Tudor 1989, Hilty 2003, 2011, Dickinson and Christidis 2014, Restall et al. 2006), a treatment finally enacted by del Hoyo and Collar (2016) on the basis of the distinctive plumage of <em>whitelyi<\/em>, and followed by Hilty (2021). [Note that, while treated within <em>Tangara<\/em>, the name <em>Tangara cyanoptera <\/em>was preoccupied by <em>Saltator cyanopterus <\/em>Vieillot, 1817 (Dickinson and Christidis 2014), and thus <em>Tangara argentea<\/em> (Lafresnaye, 1843) was used, including by del Hoyo and Collar (2016). With the move of this clade of tanagers to <em>Stilpnia<\/em>, the name <em>cyanoptera <\/em>is once again in use.]<\/p>\n\n\n\n<p>During the AviList voting process, strong differences in typical call notes were detected, and this and other striking vocal differences that evidently do not overlap were elaborated upon by P. Boesman in Remsen\u2019s <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1013.htm\">2024 SACC proposal<\/a>. The combined evidence from plumage and vocalizations has led both SACC and AviList Core Team (2025) to consider <em>whitelyi <\/em>a distinct species.<\/p>\n\n\n\n<p><strong>English names:<\/strong> As used by del Hoyo and Collar (2016), the English name Black-headed Tanager has been retained for <em>Stilpnia cyanoptera s.s.<\/em>, and Black-hooded Tanager for <em>Stilpnia whitelyi<\/em> by SACC and AviList Core Team (2025).<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Yellow-tufted Dacnis <em>Dacnis egregia<\/em> <\/strong>is split from <strong>Black-faced Dacnis <em>Dacnis lineata<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) Two South American dacnises look more similar as specimens than they do in photos or in life, and thus the distinctness of the newly split Yellow-tufted Dacnis was only recently recognized.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 35142\u201335145<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Black-faced Dacnis <em>Dacnis lineata<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>egregia, aequatorialis<\/em>, and <em>lineata<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Yellow-tufted Dacnis <em>Dacnis egregia<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>egregia<\/em> and <em>aequatorialis<\/em><\/li>\n\n\n\n<li>Black-faced Dacnis <em>Dacnis lineata<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/30-Dacnis-lineata-graphical-abstract.png\" alt=\"\" class=\"wp-image-1107 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/30-Dacnis-lineata-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/30-Dacnis-lineata-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/30-Dacnis-lineata-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/30-Dacnis-lineata-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the two species into which Black-faced Dacnis <em>Dacnis lineata <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>Originally described as two species of dacnis, <em>lineata <\/em>(Gmelin, 1789) of Amazonia and the Guianan Shield, and <em>egregia <\/em>Sclater, 1855 of the river valleys of western Colombia, a third taxon was, surprisingly (for the time), described as a subspecies of <em>egregia<\/em>, <em>aequatorialis <\/em>Berlepsch &amp; Taczanowski, 1884, of far southwestern Colombia to far northwestern Peru. Hellmayr (1935) may have been the first to consider <em>egregia <\/em>and <em>aequatorialis <\/em>as subspecies of <em>lineata<\/em>, with the statement \u201c[t]his bird, heretofore treated as a distinct species, is clearly but a geographical representative of the White-vented Dacnis [<em>lineata<\/em>], which it replaces west of the eastern Andes\u2026\u201d. Hellmayr\u2019s (1935) treatment was followed by most other authors, including Storer (1970, in Volume 13 of Peters\u2019 Check-list), until a two-way split was enacted by Ridgely and Greenfield (2001), after Ridgely and Tudor (1989) discussed the likelihood that they should be split. This treatment was that adopted by Hilty (2011, 2021), del Hoyo and Collar (2016), and the IOC-WBL (from v.3.1). Restall et al. (2006) opined that <em>egregia <\/em>(with <em>aequatorialis<\/em>) \u201cappears to be a separate species\u201d, but followed the single-species SACC treatment held at that time.&nbsp;<\/p>\n\n\n\n<p>From comments in the literature, it seems likely that the relative distinctness of <em>egregia <\/em>(including <em>aequatorialis<\/em>) from <em>lineata <\/em>is not as apparent in study skins as it is in photos. Now, large series of images are available for all, and these show <em>egregia <\/em>and <em>aequatorialis <\/em>to be quite similar to each other, but to differ strikingly in both sexes from <em>lineata <\/em>in their yellow lower underparts, and especially in the obvious yellow pectoral tufts of males, as opposed to white lower underparts and minimal white pectoral tufts in <em>lineata<\/em>. Their simple vocalizations do not differ obviously, however, which seems true of some other members of this genus as well. Genomic data seem to indicate that <em>Dacnis lineata s.l. <\/em>(including <em>egregia<\/em>) is non-monophyletic with respect to <em>Dacnis vigueri <\/em>Oustalet, 1883, but this is not well-supported (Price-Waldman 2019).<\/p>\n\n\n\n<p>AviList initially voted to retain <em>egregia <\/em>as a subspecies of <em>lineata<\/em>,<a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop103.htm\"> as had SACC in 2004<\/a>. However, after <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1014.htm\">resounding approval of the split<\/a> by SACC in 2024, a second AviList vote led to adoption of the split (AviList Core Team 2025).<\/p>\n\n\n\n<p><strong>English names:<\/strong> The long-standing English name Black-faced Dacnis for <em>Dacnis lineata <\/em>is retained for the widespread Amazonian taxon, while the highly apt and thus uncontroversial name used previously, Yellow-tufted Dacnis, is taken up for <em>Dacnis egregia<\/em>.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Pink-billed Cnemoscopus <\/strong><strong><em>Cnemoscopus rubrirostris<\/em><\/strong> and monotypic <strong>Black-billed Cnemoscopus <\/strong><strong><em>Cnemoscopus chrysogaster<\/em><\/strong> are split from <strong>Gray-hooded Bush Tanager <\/strong><strong><em>Cnemoscopus rubrirostris<\/em><\/strong><\/h4>\n\n\n\n<p><strong>Summary:<\/strong>&nbsp;(1\u21922 species) The Mara\u00f1\u00f3n Valley of northern Peru marks the boundary between another species pair, two tanagers now given the group name of \u2018Cnemoscopus\u2019.<\/p>\n\n\n\n<p><strong>Details:&nbsp;<\/strong>v2025 taxa 35432\u201335433<\/p>\n\n\n\n<p>Was:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Gray-hooded Bush Tanager <em>Cnemoscopus rubrirostris<\/em>&nbsp;<\/li>\n\n\n\n<li>subspecies <em>rubrirostris<\/em> and <em>chrysogaster<\/em><\/li>\n<\/ul>\n\n\n\n<p>Now:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pink-billed Cnemoscopus <em>Cnemoscopus rubrirostris<\/em> (monotypic)&nbsp;<\/li>\n\n\n\n<li>Black-billed Cnemoscopus <em>Cnemoscopus chrysogaster<\/em> (monotypic)<\/li>\n<\/ul>\n\n\n\n<p><strong>Graphical abstract:<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img decoding=\"async\" width=\"1280\" height=\"720\" data-src=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/31-Cnemoscopus-rubrirostris-graphical-abstract.png\" alt=\"\" class=\"wp-image-1108 lazyload\" data-srcset=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/31-Cnemoscopus-rubrirostris-graphical-abstract.png 1280w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/31-Cnemoscopus-rubrirostris-graphical-abstract-720x405.png 720w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/31-Cnemoscopus-rubrirostris-graphical-abstract-768x432.png 768w, https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-content\/uploads\/2025\/11\/31-Cnemoscopus-rubrirostris-graphical-abstract-480x270.png 480w\" data-sizes=\"(max-width: 1280px) 100vw, 1280px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 1280px; --smush-placeholder-aspect-ratio: 1280\/720;\" \/><figcaption class=\"wp-element-caption\">A map of South America showing the ranges of the two species into which Gray-hooded Bush Tanager <em>Cnemoscopus rubrirostris <\/em>is partitioned.<\/figcaption><\/figure>\n\n\n\n<p>The two tanager taxa comprising the Andean genus <em>Cnemoscopus<\/em>, <em>rubrirostris <\/em>(de Lafresnaye, 1840) of the northern Andes from northwestern Venezuela to far northwestern Peru, and <em>chrysogaster <\/em>(Taczanowski, 1875), from Peru south of the Mara\u00f1\u00f3n Valley to far western Bolivia, were originally described as full species. Hellmayr (1936), however, treated them as conspecific, stating \u201c[s]ome of the Ecuadorian specimens [of <em>rubrirostris<\/em>], by slightly larger size and darker bills, form the passage to the Peruvian <em>C. r. chrysogaster<\/em>.\u201d In fact, subsequent sources (e.g. Zimmer 1947, Schulenberg et al. 2007) state that <em>rubrirostris <\/em>is larger than <em>chrysogaster<\/em>, and ML images seem to indicate that juveniles of the former may have dark bills. Nevertheless, Storer (1970, in Volume 13 of Peters\u2019 Check-list), and nearly all other sources have treated the two as conspecific, until split by del Hoyo and Collar (2016).&nbsp;<\/p>\n\n\n\n<p>An initial consideration by AviList resulted in a decision to retain the status quo of no split. However, <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1016.htm\">a subsequent proposal by SACC<\/a>, with vocal data provided by A. Spencer, led to their split, based largely on differences in the contact calls, characterized as a dry \u2018spit\u2019 note in <em>rubrirostris<\/em>, and a \u201chigher-pitched, noticeably differently shaped, polyphonic tink note\u201d for <em>chrysogaster<\/em>. Upon reconsideration, AviList followed suit in splitting <em>chrysogaster<\/em> (AviList Core Team 2025).<\/p>\n\n\n\n<p><strong>English names:<\/strong> Given the fact that the English name used by del Hoyo and Collar (2016) of Grey-hooded Bush Tanager for <em>rubrirostris <\/em>violates the range-size policy of SACC, and that it has long been used for <em>chrysogaster <\/em>as well, it was deemed in need of change. In addition, the name Golden-bellied Tanager, which del Hoyo and Collar (2016) used for <em>chrysogaster<\/em>, could equally apply to both (though it does mirror the specific epithet). <a href=\"https:\/\/www.museum.lsu.edu\/~Remsen\/SACCprop1042.htm\">After much discussion<\/a>, the English names settled upon were Pink-billed Cnemoscopus for <em>Cnemoscopus rubrirostris<\/em>, and Black-billed Cnemoscopus for <em>Cnemoscopus chrysogaster<\/em>. This highlights the most obvious difference between them, bill color, and avoids confusion with the distantly related Gray-headed Tanager <em>Eucometis penicillata<\/em>.<\/p>\n\n\n\n<div class=\"wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link wp-element-button\" href=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/updates-and-corrections-october-2025-page-2\/\">Continue to Page 2<\/a><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>This document accompanies the eBird\/Clements Checklist v2025 spreadsheet (tap or click link for downloads and recommended citation). Note the following: Species Gains and Losses Splits Red Grouse Lagopus scotica is split from Willow Ptarmigan Lagopus lagopus Summary:&nbsp;(1\u21922 species) The Red Grouse, endemic to the British Isles, differs from all other taxa of Willow Ptarmigan in<a class=\"excerpt-read-more\" href=\"https:\/\/www.birds.cornell.edu\/clementschecklist\/updates-and-corrections-october-2025\/\" title=\"ReadUpdates and Corrections\u2014October 2025\">&#8230; Read more &raquo;<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_birdpress_hero_toggle":false,"_birdpress_hero_type":"image","_birdpress_hero_image_type":"image","_birdpress_hero_style":"default","_birdpress_hero_ratio":"","_birdpress_hero_h1":"","_birdpress_hero_media_id":0,"_birdpress_hero_media_array_id":[],"_birdpress_hero_media_array":[],"_birdpress_hero_media":0,"_birdpress_hero_video_id":0,"_birdpress_hero_video":0,"_birdpress_hero_youtube":"","_birdpress_hero_content":true,"_birdpress_hero_byline":"","_birdpress_hero_byline_bottom":"","_birdpress_hero_button_link":"","_birdpress_hero_button_text":"","_birdpress_hero_button_color":"","_birdpress_hero_date":false,"original_guid":"","_birdpress_hide_search":false,"_birdpress_page_width":"","_birdpress_global_cta":false,"_birdpress_widget_sidebar":"","_birdpress_next_article":0,"_birdpress_next_article_title":"","_birdpress_prev_article":0,"_birdpress_prev_article_title":"","_birdpress_sub_navigation_id":0,"_birdpress_sub_navigation":"","_birdpress_sub_navigation_title":false,"_birdpress_anchor_navigation_id":16,"_birdpress_anchor_navigation":"October 2025 Updates & Corrections","_birdpress_postType":"both","_birdpress_categoryID":0,"_birdpress_tagID":0,"_birdpress_parentPostID":0,"_birdpress_parentPostTitle":"","_birdpress_menuID":0,"_birdpress_menuName":"","_birdpress_listHeader":"","_birdpress_listLayout":"card-display","_birdpress_listColumns":"","_birdpress_maxItems":12,"_birdpress_listPaginate":true,"_birdpress_displaySort":true,"_birdpress_sortOrder":"DESC","_birdpress_sortBy":"date","_birdpress_listID":"","_birdpress_listClass":"","_birdpress_displayImages":true,"_birdpress_displayCaptions":false,"_birdpress_displayExcerpts":false,"_birdpress_attTop":"","_birdpress_attBottom":"","_birdpress_showLogos":false,"_birdpress_post_logo":0,"footnotes":""},"class_list":["post-1245","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/pages\/1245","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/comments?post=1245"}],"version-history":[{"count":0,"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/pages\/1245\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.birds.cornell.edu\/clementschecklist\/wp-json\/wp\/v2\/media?parent=1245"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}