Back to: List 1 List 2 List 3 List 4 List 5 List 6.
| 01 The order Anseriformes is now placed after Ostrich according to modern systematics. (2003) |
| 02 Split from B. canadensis. Based on morphology, ecological factors and genetics. (2007) |
| 03 New in Category C. (2000). Changed scientific name to Alopochen aegyptiaca. (2003) |
| 04 Changed English name from Cotton Pygmy-goose, following Gill & Wright. (2006) |
| 05 Also called Eurasian Teal. (Gill & Wright 2006) |
| 06 Split from Anas crecca, based on morphology and genetics. Preliminary DNA results show that Green-winged Teal is more related to the South American species A. flavirostris. (2003) |
| 07 Includes the form diazi, "Mexican Duck." (1995) |
| 08 Swedish name adjusted from bahamaand to bahamasand, named after the Bahamas. (2007) |
| 09 Split from M. nigra, based on bill structure and vocalization. Also called American Scoter, but occurs also in Asia. (2007) |
| 10 Split from M. fusca, based on bill structure and vocalization. (2007) |
| 11 Placed in the genus Lophodytes by Beaman. (1995) |
| 12 Placed in the genus Mergellus by Beaman. (1995) |
| 13 Also called Common Merganser. (Gill & Wright 2006) |
| 14 New in Category C. (2000) |
| 15 The order Galliformes is now placed after Anseriformes according to modern systematics. (2003) |
| 16 The genus Dendragapus is considered paraphyletic, but relation to Tetrao unclear. (2007) |
| 17 The genus Dendragapus is considered paraphyletic. Present species sometimes regarded as superspecies with Siberian Grouse. (2007) |
| 18 Changed name from Blue Grouse, D. obscurus (blåjärpe) because of a split (2007) |
| 19 Split from D. obscurus, based on vocalization, behaviour, morphology and genetics. (2007) |
| 20 Swedish name adjusted from kinajärpe to kinesisk järpe, following conventional Swedish. (2007) |
| 21 The Scottish form of Willow Ptarmigan gets the scientific name Lagopus lagopus scotica. (2003) |
| 22 Changed species epithet from mutus to muta. (2003) |
| 23 Also called Greater Sage-grouse. (2007) |
| 24 Split from C. urophasanius. Also called Gunnison Sage-grouse. (2007) |
| 25 Previously treated as a race of C. coturnix. (1995) |
| 26 Changed English name from Boulton's Hill Partridge. (2007) |
| 27 The Japanese race versicolor sometimes treated as a separate species (grön fasan) based on hybrid zone studies in Japan (1995 and 2007). |
| 28 Gaviiformes and following orders in the same systematic order as before. |
| 29 Previously treated as a race of G. arctica. (1995) |
| 30 Previously treated as a race of A. occidentalis. (1995) |
| 31 Changed generic name to Thalassarche. (2003) |
| 32 Not named after the West Indian island Trinidad (1995). Trinidade (or Trindad in Portugese) is an island in the South Atlantic. English name changed from South Trinidad Petrel. (2007) |
| 33 Previously treated as a race of P. mollis.
(1995). |
| 34 Also called Cahow. (2007) |
| 35 Sometimes treated as two species; Hawaiian P. and Galapagos P., but it is not clear which of the forms that has been recorded in the Holarctic region. (2007) |
| 36 Sometimes treated as a race of P. externa. (1995) |
| 37 Mediterranean Shearwater is split into two monotypic species: Yelkouan Shearwater, Puffinus yelkouan, resident i many parts of the Mediterranean, and Balearic Shearwater, Puffinus mauretanicus, breeding in the Balearics. The split is based on differences in morphology, vocalization, genetic data, feeding behaviour and the breeding period. (2003) |
| 38 Named after the peninsula Baja California. (1995) |
| 39 Mascarene Shearwater, P. atrodorsalis deleted. Not a valid species. The described specimen was a young Puffinus bailloni. (2007) |
| 40 Northern Gannet gets the scientific name Morus bassanus. Based on a mt-DNA study of the whole gannet complex it was shown that there are three old branches of gannets, which is best represented by three different genus, rather than one. Cape Gannet, Morus capensis, and M. serrator in Australia is closely related to Northern Gannet, while Brown Booby, Sula leucogaster and Masked Booby, Sula dactylatra, belongs to another branch. (2003) |
| 41 Also called Japanese Cormorant. (2007) |
| 42 Previously called Ph. olivaceus, Olivaceous Cormorant. (1995) |
| 43 A record from Scotland 1953 re-identified as this species in 2003. (2007) |
| 44 Rufous Night Heron (N. caledonicus) deleted from the list. (2007) |
| 45 The scientific name of Striated Heron is changed to Butorides striata. Also the Swedish name is changed from grönhäger. (2003) |
| 46 The Swedish name is changed from lotushäger. (2003) |
| 47 Previously placed with C. ciconia. (1995) |
| 48 Greater Flamingo is split in two species; Greater Flamingo, Phoenicopterus roseus, distributed in Europe, Africa and Asia, and Caribbean Flamingo, Ph. ruber, distributed in the West Indies and Central America. The separation is based on differences in morphology, including plumage, bill and leg coloration, and also on lek calls and other calls. (2003) |
| 49 Sometimes treated as a race of P. apivorus. (1995) |
| 50 Previously sometimes treated as a race of E. caeruleus. (1995) |
| 51 Previously a race of C. aeruginosus. (1995) |
| 52 Swedish name kinahök adjusted to kinesisk sparvhök. (2007) |
| 53 Changed order of Aquila eagles due to several investigations of the genetic relationships. (2007) |
| 54 Changed from Hieraaetus pennatus. Genetic studies has showed that either Aquila nor Hieraaetus were monophyletic. With this rearrangement Aquila gets monophyletic. (2007) |
| 55 Changed from Hieraaetus fasciatus. Genetic studies has showed that either Aquila nor Hieraaetus were monophyletic. With this rearrangement Aquila gets monophyletic. (2007) |
| 56 Previously merged with A. rapax. (1995) |
| 57 Includes the form vindiana. (1995) |
| 58 Imperial Eagle is split in two species: Eastern Imperial Eagle, Aquila heliaca, distributed in East Europe and Asia, and Spanish Imperial Eagle, A. adalberti, on the Iberian Peninsula. The split is based on differences in morphology (including clear differences in juvenile and subadult plumage), genetic data and small but constant differences in structure among adults. (2003) |
| 59 Crested Caracara, Polyborus plancus, split in two species, the northern species occurs in North America. (2007) |
| 60 Previously treated as a race of F. vespertinus. (1995) New for Sweden 2005. |
| 61 Includes the form altaicus. (1995) |
| 62 Sometimes treated as a race of F. peregrinus. (1995) |
| 63 Changed scientific name to Turnix sylvaticus. (2003) |
| 64 Buttonquails in Gill & Wright 2006. |
| 65 Sometimes placed in the genus Gallirallus. (1995) |
| 66 Sometimes placed in the genus Aenigmatolimnas. (1995) |
| 67 Sometimes placed in the genus Amaurornis. (1995) |
| 68 Changed genus to Porphyrio. (2007) |
| 69 Changed scientific name from Porphyrula martinica. (2007) |
| 70 Also includes African and Asian races. (1995) |
| 71 Demoiselle Crane will get the scientific name Grus virgo. Two independent studies of crane genetics shows that this species don’t differ considerably from species within the genus Grus. (2003) |
| 72 Houbara Bustard is split in two species: Houbara Bustard, Chlamydotis undulata, with distribution in North Africa including Fuerteventura, and Macqueen’s Bustard, C. macqueenii, from Middle East to Asia. The split is based on differences in morphology, display behaviour and genetic data. (2003) |
| 73 The word jasaná originates from the Tupi, then becomes jaçana in Portugese. The latter is pronounced jassana, but has become distorted via English to jakana. (2007) |
| 74 Changed English name from Greater Painted-snipe. (2007) |
| 75 Sometimes merged with H. himantopus. (1995) |
| 76 Sometimes treated as a race of C. hiaticula. (1995) |
| 77 Chestnut-banded Sand Plover, Ch. pallidus (sodasjöpipare) deleted. The Israeli record rejected. (2007). |
| 78 Split from P. dominica. (1995) |
| 79 Sometimes placed in the genus Hoplopterus. (1995) |
| 80 Sometimes placed in the genus Chettusia. (1995) |
| 81 New for Sweden 2005. |
| 82 Changed genus to Calidris. The resons for placing Stilt Sandpiper in a separate genus are weak. (2003) |
| 83 Common Snipe is separated in two species: Common Snipe, Gallinago gallinago, distributed in the Old World, and Wilson’s Snipe, G. delicata, distributed in North America. The split is based on differences in morphology, the display call made by the outer tail feathers, and possibly also genetic data. (2003) |
| 84 English name changed from Pintail Snipe (it is not similar to the duck Pintail). (2007) |
| 85 New for Sweden 2005. |
| 86 Changed species epithet from macularia. (2003) |
| 87 Changed species epithet from fulicaria. (2003) |
| 88 Changed English name from Jaeger to Skua after merging of the larger skuas to Stercorarius. Also because Pomarine and Great are closely related. (2007) |
| 89 Changed Swedish name from labb to kustlabb. (2003) |
| 90 Changed generic name from Catharacta. Based on morphology, ectoparasites and genetics. (2007) |
| 91 Larus argentatus is split into 4 species, based on differences in morphology, calls, display behaviour and established reproductive barriers. (2003) |
| 92 Split from Larus argentatus. (2003) |
| 93 Split from Larus argentatus. Placed before armenicus because it was described 1811, armenicus 1840. (2003) |
| 94 Includes the forms thayeri and kumlieni. (1995) |
| 95 The systematic order of the terns has been changed due to a revision by Bridge et al. 2005.. |
| 96 The genus Sterna has been revised by Bridge et al. 2005. Changed scientific name, from Sterna aleutica. (2007) |
| 97 Changed scientific name, from Sterna lunata. (2007) |
| 98 Changed scientific name, from Sterna fuscata. (2007) |
| 99 Changed scientific name, from Sterna anaethetus. (2007) |
| 100 The race saundersi sometimes treated as a separate species (persisk småtärna). (1995) |
| 101 Sometimes treated as a race of S. albifrons. (1995) |
| 102 Sterna nilotica gets back it's older name Gelochelidon nilotica. (2007) |
| 103 Sterna caspia gets back it's older name Hydroprogne caspia. (2007) |
| 104 Changed species epithet from hybridus. (2003) |
| 105 The remaining terns in Sterna are now considered a monophyletic group. (2007) |
| 106 Has been called S. zimmermanni. (1995) |
| 107 Split from B. marmoratus, based on differences in morphology and genetics. (2003) |
| 108 Changed scientific name, from Cyclorrhynchus psittacula. (2003) |
| 109 The feral form (often called Ringed Turtle Dove, S. risoria), breeds locally in North America. (1995) |
| 110 Swedish name kinaparakit adjusted to kinesisk parakit. (2007) |
| 111 Hierococcyx sometimes merged into genus Cuculus. (1995) |
| 112 Split from Hodgsons's Hawk Cuckoo, together with H. fugax (malajisk hökgök), the latter is extralimital. (2007) |
| 113 Former name in Swedish: mindre guldgök. (2007) |
| 114 Former name in Swedish: större guldgök. (2007) |
| 115 Changed English name, from Oriental Cuckoo, due to split. Also the Swedish name changed, from taigagök. The latter name instead applied on Cuculus optatus. (2007) |
| 116 Oriental Cuckoo, Cuculus saturatus, is split into three species; Horsfield's Cuckoo, C. optatus, Himalayan Cuckoo, C. saturatus and the extralimital C. lepidus. C. optatus Gould 1845 has priority over C. horsfieldi Moore 1857.(2007) |
| 117 Proposed split into several species, but more research on Otus taxonomy needed. (2007) |
| 118 Changed generic name, from Otus to Megascops, on all American screech-owls except one. (2007) |
| 119 Changed scientific name, from Nyctea scandiaca. Osteological and genetic studies shows it to be closely related to Bubo bubo. (2003) |
| 120 Split from N. scutulata, based on vocalization and morphology. (2007) |
| 121 The form davidi sometimes treated as a separate species. (1995) |
| 122 Sometimes placed in the genus Nephoecetes. (1995) |
| 123 Breeds in Oman. New to the Holarctic region. Also called somaliseglare in Swedish, but Tk prefers full country names instead of shortened. (2007) |
| 124 Changed name to Eared Quetzal by AOU, but not a true quetzal (i.e. Pharomachrus). (2007) |
| 125 The extinct H. miyakoensis (miyakokungsfiskare) is now considered belonging to this species. (1995) |
| 126 Previously often treated as the same species as M. superciliosus. (1995) |
| 127 Previously treated as a race of P. viridis. (1995) |
| 128 All North American Dendrocopos woodpeckers moved to genus Picoides. Picoides is a monophyletic group, separated from Dendrocopos based on morphology, vocalization, behavoiur and ecological data. (2007) |
| 129 Arizona Woodpecker, P. arizonae is sometimes split from D. stricklandi (stricklandi then becomes extralimital), based on morphology, behaviour and breeding habitat. (2007) |
| 130 Proposed split to Eurasian Three-toed Woodpecker and American Three-toed Woodpecker, but the differences are minor. (2007) |
| 131 The Swedish name empid is formed of the scientific generic name. (1995) |
| 132 White-throated Flycatcher (Empidonax "pacificus", kustempid) is deleted from the list and replaced with this species. (2007) |
| 133 Sometimes merged with P. moluccensis (blåvingad pitta). (1995) |
| 134 Changed species epithet, following nomenclatural revision. (2007) |
| 135 Changed species epithet, from cincturus. (2003) |
| 136 Changed Swedish name, from båglärka. (2003) |
| 137 Sometimes merged with C. cinerea (rödkronad lärka). (1995) |
| 138 Changed Swedish name from höglandslärka to Humes korttålärka. (2007) |
| 139 The race cheleensis and some other closely related forms are sometimes considered separate species. (1995) |
| 140 Named after the island Razo (spelt Raso in English). (1995) |
| 141 Split from Riparia riparia, based on morphology and genetics. (2007) |
| 142 The genus Hirundo is revised, to become monophyletic. Hirundo fuligula is changed to Ptyonoprogne fuligula. (2007) |
| 143 Hirundo rupestris is changed to Ptyonoprogne rupestris. (2007) |
| 144 Hirundo daurica is changed to Cecropis daurica. (2007) |
| 145 Hirundo fluvicola is changed to Petrochelidon fluvicola (2007) |
| 146 Hirundo fulva is changed to Petrochelidon fulva (2007) |
| 147 Hirundo pyrrhonota is changed to Petrochelidon pyrrhonota. (2007) |
| 148 Changed species epithet from urbica. (2003) |
| 149 Previously placed in the Anthus novaezeelandiae complex. (1995) |
| 150 Previously placed in the Anthus novaezeelandiae complex. (1995) |
| 151 Previously treated as a race of A. spinoletta. (1995) |
| 152 Previously treated as a race of A. spinoletta. (1995) One of each race recorded in Sweden (japonicus 1997, rubescens 2005). |
| 153 The systematics is complicated and the relationships among the many races are unclear. Includes among others; feldegg, flavissima, lutea and taivana. (1995) |
| 154 Includes the forms lugens and personata. The systematics is complex and the relationships between the different forms partially unclear. (1995) |
| 155 Split from Rosy Minivet, P. roseus. (2007) |
| 156 Swedish name kinabulbyl adjusted to kinesisk bulbyl. (2007) |
| 157 Sometimes treated as a race of P. leucogenys (himalayabulbul). (1995) |
| 158 Considered to be separated from H. madagascariensis. (1995) |
| 159 Previously called T. dorsale. (1995) |
| 160 Changed from erythronota and Evermann's. (2007) |
| 161 Changed from coeruleocephalus. (2007) |
| 162 Changed from erythrogaster. (2003) |
| 163 Changed from macrorhyncha, due to revised nomenclature by David & Gosselin. (2007) |
| 164 Includes the race group maura, sometimes given species status. (1995) Changed species epithet from torquata. (2003) Breeding in Sweden 2006. |
| 165 Changed from ferrea. (2007) |
| 166 Previously treated as a race of O. pleschanka (nunnestenskvätta). (1995). Also called Cyprus Pied Wheatear. (2007) |
| 167 Also called Kurdish Wheatear or Red-tailed Wheatear. (2007) |
| 168 Split from Oe. xanthoprygmna (2003). Also called Red-tailed Wheatear. (2007) |
| 169 Changed from alboniger. (2007) |
| 170 Changed from rufocinerea. (2007) |
| 171 Consisting of a number of forms which probably will be split in the future. (1995) |
| 172 Previously merged with Z. dauma (guldtrast). (1995) |
| 173 Sometimes placed in genus Ixoreus, based on mt-DNA analysis. (2007) |
| 174 Split from C. minimus, based on morphology, vocalization and genetics. (2003) |
| 175 Swedish name kinatrast changed to kinesisk trast. (2007) |
| 176 Includes the form canturians, sometimes treated as a separate species. (1995) |
| 177 Previously treated as a race of B. thorasicus (fläckig smygsångare). (1995) |
| 178 The form pleskei regarded as separated species in Beaman. (1995) |
| 179 Ringed juveniles in Sweden 2005. |
| 180 Sometimes placed in the genus Locustella. (1995) |
| 181 Split from A. agricola, based on morpholgy and genetics. (2003) |
| 182 3 fledglings recorded in Sweden 2005 |
| 183 Also called Cape Verde Cane Warbler or Cape Verde Bush-warbler. (2007) |
| 184 Also called Eurasian Reed Warbler. (Gill & Wright) |
| 185 Split from A. arundinaceus, based on ault and juvenile morphology. (2003) |
| 186 Sometimes merged with A. arundinaceus (trastsångare). (1995) |
| 187 Changed back to previous English name, from Eastern Olivaceous Warbler. (2007) |
| 188 Split from H. pallida, based on morphology, vocalization, behaviour and genetics. (2003). Changed English name, from Western Olivaceous Warbler. (2007) |
| 189 New Swedish name due to split, before split called gråsångare in Swedish, which was a misleading name of these brown birds. (2003) |
| 190 Split from H. caligata, based on morphology, vocalization, ecology, genetics and partly sympatric breeding. (2003) |
| 191 Split from Sylvia sarda, based on morphology, vocalization and genetics. (2003) |
| 192 Changed English name, due to split. (2003) |
| 193 Split from Sylvia nana, based on morphology and vocalization. (2003) |
| 194 Changed Swedish and English names due to split. (2003) |
| 195 Split from S. hortensis based on small but constant differences in morphology, and clear differences in song and genetics. (2003) |
| 196 Includes the forms althaea and minula, sometimes treated as full species. (1995) |
| 197 Split into six species, five of them occuring in the Holarctic region. Changed Swedish name from Orientalisk bambussångare. (2007) |
| 198 Split of S. burkii. Seicercus valentini is named in Swedish after the Russian ornithologist V. Bianki. (2007) |
| 199 Split of S. burkii. The mountain is transcribed Emei in modern English, not Omei. (2007) |
| 200 Previously merged with Ph. tenellipes (drillsångare). (1995) |
| 201 Ph. nitidus (kaukasisk lundsångare) and Ph. plumbeitarsus (östlig lundsångare) are sometimes treated as full species. (1995) |
| 202 Previously treated as a race of Ph. proregulus (kungsfågelsångare). (1995) |
| 203 Split of Ph. chloronotus, based on genetics, vocalization and morphology. (2007) |
| 204 A newly described species. (1995) |
| 205 A newly described species. (1995) Changed name from Ph. sichuanensis to Ph. yunnanensis due to priority rules. (2007) |
| 206 Previously treated as a race of Ph. inornatus (taigasångare). Includes the eastern race mandelli. (1995) |
| 207 Changed English name due to split. (2003) |
| 208 Split from Ph. bonelli, based on morphology, vocalization and genetics. (2003) |
| 209 The form tristis has been suggested separate species. (1995) |
| 210 Split from Ph. collybita. Called Canary Island Chiffchaff by TAC, not a proper name. (2003) |
| 211 Split from Ph. collybita. (2003) |
| 212 Includes the race teneriffae, sometimes treated as a race of R. ignicapillus or as a separate species. (1995) |
| 213 Species epithet changed, from ignicapillus. (2003) |
| 214 Split from R. ignicapilla, based on morphology, osteology, vocalization and genetics. (2003) |
| 215 Previosly merged with P. melanura (svartstjärtad myggsnappare). (1995) |
| 216 Sometimes placed in the genus Muscicapa. (1995) |
| 217 Previously called M. latirostris. (1995) |
| 218 Split from F. parva, based on morphology, vocalization, genetics and partially sympatric breeding. (2003) |
| 219 Sometimes treated as a race of F. narcissina (gulbrynad narcissflugsnappare). (1995) |
| 220 Split from F. hypoleuca, based on morphology (mainly male morphology), vocalization and genetics. (2003) |
| 221 A newly described species. (1995) |
| 222 Changed species epithet, from caudatus. (2003) |
| 223 Changed species epithet, from fulvus. (2003) |
| 224 Sometimes treated as a race of G. lunulatus (bandad fnittertrast). (1995) |
| 225 Named after the region Sikang (sometimes spelt Sikiang), not after the province Sinkiang. (1995) |
| 226 Sometimes treated as a race of A. nipalensis (himalayabandvinge). (1995) |
| 227 Previously merged with A. cinereiceps (gråhuvad fulvetta). (1995) |
| 228 Includes the eastern form hypermelaena, sometimes treated as a separate species. (1995) |
| 229 The race group hyrcanus sometimes treated as a separate species. (1995) |
| 230 Includes the songarus group, sometimes treated as a separate species. (1995) |
| 231 Split again from P. bicolor, based on genetics, vocalization and hybrid zone. (2007) |
| 232 Changed English name, from Plain Titmouse, due to split. Also the Swedish name changed from västlig gråmes to ekmes. (2007) |
| 233 Split from P. inornatus, based on morphology, vocalization and genetics. (2007) |
| 234 Also called Grey Crested Tit. (2007) |
| 235 Changed English name, from Blue Tit, due to split. (2003) |
| 236 Split from P. caeruleus, based on morphology, vocalization and genetics. (2003) |
| 237 Includes the form flavipectus. (1995) |
| 238 Moved from the ground jays to the tits, based on genetics. Changed English name from Hume's Ground Jay to Hume's Ground Tit. (2007) |
| 239 Sometimes treated as a race of S. europea (nötväcka). (1995) |
| 240A newly described species, forming a superspecies together with C. discolor. (2007) |
| 241 Interbreeding with C. familiaris in Sweden. |
| 242 Includes the forms macronyx, coronatus and consibrinus. (1995) |
| 243 Changed species epithet, from senegala. (2003) |
| 244 Split from L. excubitor, based on morphology, behaviour, habitat choice and partially sympatric breeding. (2003) |
| 245 Swedish name kinavarfågel changed to kinesisk varfågel. (2007) |
| 246 Split from A. coerulescens, based on morphology, behaviour and genetics. May be split even further. (2007) |
| 247 Split from A. coerulescens, based on morphology, behaviour and genetics. (2007) |
| 248 Changed Swedish and English name, from Snårskrika (Scrub Jay), due to split into three species. (2007) |
| 249 The western form sinaloae now considered specifically distinct (as Sinaloa Crow). (1995) |
| 250 Includes the form italiae (italiensk sparv), previously considered specifically distinct. (1995) |
| 251 Placed in the genus Carpospiza by Beaman. (1995) |
| 252 Sometimes placed in the genus Lonchura. (1995) |
| 253 Changed species epithet, from atricapillus. (2003) |
| 254 Split from V. solitarius, based mainly on genetics. (2007) |
| 255 Changed English name, from Solitary Vireo, due to split. (2007) |
| 256 The western form swainsonii has been suggested as a separate species. In that case the Swedish names will be; östlig sångvireo and västlig sångvireo. (1995) |
| 257 Split from S. citrinella, based on morphology, vocalization and genetics. The scientific name is S. corsicanus. (2003) Carduelis corsicana in G&W. |
| 258 A disputed form, previously treated either as Parrot or Common Crossbill. (1995) |
| 259 A newly described species. (1995) |
| 260 Changed species epithet, from sanguinea. (2003) |
| 261 Includes the forms murina, griseiventris and cineracea. (1995) |
| 262 Sometimes placed in the genus Coccothraustes. (1995) |
| 263 Changed name from aurocapillus, due to revised nomenclature. (2007) |
| 264 Changed English name, from Rufous-sided Towhee, due to split. (2003) |
| 265 Split from P. erythrophthalmus. (2003) |
| 266 Split from P. fuscus. (1995) |
| 267 Split from A. caudacutus, based on morphology, vocalization, breeding habitat and low grade of hybridization. (2007) |
| 268 Also called Saltmarsh Sharp-tailed Sparrow. (2007) |
| 269 Previously treated as a race of E. cia. (1995) |
| 270 Changed English name, from Striated Bunting. (2007) |
| 271 Split from E. striolata, based on morphology and vocalization. (2003) |
| 272 Changed generic name, based on two new gentical studies. (2003) |
| 273 Moved from Guiraca to Passerina, based on close relationship with P. amoena. (2007) |
| 274 Changed English name, from Northern Oriole, due to split. (2003) |
| 275 Split from I. galbula. (2003) |
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