Ansériformes
Anseriformes
148 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Linnaeus (1758) | 37 | 14,86% | 6 | 4,88% | 6 | 5,88% | 4 | 3,64% |
| Levesque & Delcroix (2018) | 22 | 8,84% | 21 | 17,07% | 19 | 18,63% | 21 | 19,09% |
| Etcheberry & Abraham (2009) | 19 | 7,63% | 16 | 13,01% | 16 | 15,69% | 13 | 11,82% |
| Commecy et al. (2013) | 18 | 7,23% | 15 | 12,2% | 15 | 14,71% | 15 | 13,64% |
| Uicn et al. (2017) | 18 | 7,23% | 15 | 12,2% | 14 | 13,73% | 13 | 11,82% |
| Questel (2020) | 15 | 6,02% | 15 | 12,2% | 12 | 11,76% | 15 | 13,64% |
| UICN Comité français, OFB & MNHN (2021) | 13 | 5,22% | 13 | 10,57% | 13 | 12,75% | 11 | 10% |
| Yokoyama (2013) | 12 | 4,82% | 8 | 6,5% | 8 | 7,84% | 6 | 5,45% |
| Gmelin (1789) | 10 | 4,02% | 3 | 2,44% | 3 | 2,94% | 2 | 1,82% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 10 | 4,02% | 3 | 2,44% | 3 | 2,94% | 2 | 1,82% |
| Questel & Le Quellec (2012) | 10 | 4,02% | 7 | 5,69% | 7 | 6,86% | 5 | 4,55% |
| Del Hoyo & Collar (2014) | 9 | 3,61% | 5 | 4,07% | 5 | 4,9% | 5 | 4,55% |
| Weimerskirch et al. (2009) | 8 | 3,21% | 5 | 4,07% | 5 | 4,9% | 2 | 1,82% |
| Belfan & Conde (2016) | 7 | 2,81% | 7 | 5,69% | 7 | 6,86% | 7 | 6,36% |
| Gonzalez et al. (2009) | 7 | 2,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2020) | 7 | 2,81% | 7 | 5,69% | 7 | 6,86% | 7 | 6,36% |
| Remsen et al. (2013) | 6 | 2,41% | 5 | 4,07% | 5 | 4,9% | 4 | 3,64% |
| Tostain et al. (2013) | 6 | 2,41% | 4 | 3,25% | 3 | 2,94% | 4 | 3,64% |
| Vieillot (1816) | 6 | 2,41% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Latham (1801) | 5 | 2,01% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Dubois et al. (2008) | 4 | 1,61% | 4 | 3,25% | 4 | 3,92% | 4 | 3,64% |
| Levesque & Delcroix (2016) | 4 | 1,61% | 4 | 3,25% | 2 | 1,96% | 4 | 3,64% |
| Gayet et al. (2010) | 3 | 1,2% | 3 | 2,44% | 3 | 2,94% | 3 | 2,73% |
| Linnaeus (1766) | 3 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| CHN (2017) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Clements et al. (2015) | 2 | 0,8% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Combrisson (1999) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Cowles (1994) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dickinson & Remsen (2013) | 2 | 0,8% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Donovan (1816) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois & Cugnasse (2015) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Dubois (2007) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Eyton (1838) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gallien (2008) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Georgi (1775) | 2 | 0,8% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Green (1996) | 2 | 0,8% | 2 | 1,63% | 0 | 0% | 2 | 1,82% |
| Jardine & Selby (1826-1835) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1790) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Molina (1782) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olson & Jouventin (1996) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Pallas (1769) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reichenow (1904) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rocamora (2004) | 2 | 0,8% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Rüppell (1845) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Safford & Hawkins (2013) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Scopoli (1769) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swainson & Richardson (1831) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2014) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 1 | 0,91% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Uicn et al. (2015) | 2 | 0,8% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Uicn et al. (2015) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 1 | 0,91% |
| Uicn et al. (2016) | 2 | 0,8% | 2 | 1,63% | 2 | 1,96% | 2 | 1,82% |
| Wilson (1814) | 2 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Baillon (1834) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barau et al. (2005) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bechstein (1803) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2016) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Birdlife International (2017) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Bonaparte (1850) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonfils (2024) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Brewster (1902) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brunet (2022) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Buller (1869) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Calenge et al. (2010) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Cantera (2007) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Clergeau & Lorvelec (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Clergeau & Lorvelec (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Clergeau & Vigne (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Clergeau et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Clergeau et al. (2003) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clergeau et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Contejean (2018) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Costrel & Corainville (1929) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Crochet et al. (2022) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Dalgety & Scott (1948) | 1 | 0,4% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Dreff & Delliere (1994) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forster (1781) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Furminieux (2019) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Gargominy et al. (1996) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Gill (1995) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Gmelin (1788) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Graber & Euzeby (1976) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Güldenstädt (1770) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gyimesi & Lensink (2012) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Hartlaub & Finsch (1872) | 1 | 0,4% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Horsfield (1824) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Issa & Muller (2015) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Kempen van (1905) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lawrence (1848) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemarinel (2019) | 1 | 0,4% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Lemetteil (1880) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1766) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Clergeau (2003) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Vigne (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Lorvelec & Vigne (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Maksimova (1976) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Menegaux (1909) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Ménétries (1832) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Newton & Gadow (1893) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| pallas (1764) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1773) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal & Clergeau (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Pascal et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Pascal et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Poeppig (1829) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poisson (1925) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Potin (2013) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Questel (2023) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stahl et al. (1984) | 1 | 0,4% | 1 | 0,81% | 0 | 0% | 1 | 0,91% |
| Swinhoe (1871) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Triplet et al. (2003) | 1 | 0,4% | 1 | 0,81% | 1 | 0,98% | 1 | 0,91% |
| Zilli (2021) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| (1994) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
