Pélécaniformes
Pelecaniformes
143 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Uicn et al. (2017) | 38 | 15,02% | 38 | 28,79% | 31 | 34,83% | 26 | 23,64% |
| Levesque & Delcroix (2018) | 23 | 9,09% | 23 | 17,42% | 16 | 17,98% | 17 | 15,45% |
| Remsen et al. (2013) | 23 | 9,09% | 23 | 17,42% | 23 | 25,84% | 13 | 11,82% |
| Gmelin (1789) | 21 | 8,3% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Linnaeus (1758) | 21 | 8,3% | 7 | 5,3% | 7 | 7,87% | 5 | 4,55% |
| UICN Comité français, OFB & MNHN (2021) | 20 | 7,91% | 20 | 15,15% | 20 | 22,47% | 8 | 7,27% |
| Uicn et al. (2015) | 17 | 6,72% | 17 | 12,88% | 17 | 19,1% | 8 | 7,27% |
| Questel & Le Quellec (2012) | 15 | 5,93% | 15 | 11,36% | 12 | 13,48% | 8 | 7,27% |
| Questel (2020) | 14 | 5,53% | 14 | 10,61% | 10 | 11,24% | 9 | 8,18% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 13 | 5,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 13 | 5,14% | 13 | 9,85% | 12 | 13,48% | 3 | 2,73% |
| Belfan & Conde (2016) | 11 | 4,35% | 11 | 8,33% | 6 | 6,74% | 8 | 7,27% |
| Weimerskirch et al. (2009) | 11 | 4,35% | 10 | 7,58% | 9 | 10,11% | 3 | 2,73% |
| Rocamora (2004) | 10 | 3,95% | 9 | 6,82% | 7 | 7,87% | 6 | 5,45% |
| Linnaeus (1766) | 8 | 3,16% | 4 | 3,03% | 3 | 3,37% | 3 | 2,73% |
| Clements et al. (2015) | 7 | 2,77% | 7 | 5,3% | 3 | 3,37% | 6 | 5,45% |
| Clements (2012) | 7 | 2,77% | 7 | 5,3% | 3 | 3,37% | 6 | 5,45% |
| Dickinson & Remsen (2013) | 6 | 2,37% | 6 | 4,55% | 1 | 1,12% | 6 | 5,45% |
| Tostain et al. (2013) | 6 | 2,37% | 6 | 4,55% | 6 | 6,74% | 4 | 3,64% |
| Uicn et al. (2020) | 6 | 2,37% | 6 | 4,55% | 6 | 6,74% | 4 | 3,64% |
| Gill (1995) | 5 | 1,98% | 5 | 3,79% | 5 | 5,62% | 0 | 0% |
| Safford & Hawkins (2013) | 5 | 1,98% | 5 | 3,79% | 2 | 2,25% | 3 | 2,73% |
| Barau et al. (2005) | 4 | 1,58% | 4 | 3,03% | 3 | 3,37% | 1 | 0,91% |
| Dubois et al. (2008) | 4 | 1,58% | 4 | 3,03% | 4 | 4,49% | 4 | 3,64% |
| Thibault et al. (2014) | 4 | 1,58% | 4 | 3,03% | 4 | 4,49% | 1 | 0,91% |
| Commission de l’Avifaune Française (2016) | 3 | 1,19% | 3 | 2,27% | 3 | 3,37% | 0 | 0% |
| Dodson & Fitzgerald (1980) | 3 | 1,19% | 2 | 1,52% | 0 | 0% | 2 | 1,82% |
| Etcheberry & Abraham (2009) | 3 | 1,19% | 3 | 2,27% | 3 | 3,37% | 1 | 0,91% |
| Lesson (1831) | 3 | 1,19% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Mathews (1914) | 3 | 1,19% | 2 | 1,52% | 1 | 1,12% | 2 | 1,82% |
| Barre et al. (2009) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Blumenbach (1810) | 2 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosc (1792) | 2 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chartier et al. (2007) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 0 | 0% |
| Commecy et al. (2013) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Cowles (1994) | 2 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daniel et al. (2020) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 0 | 0% |
| Ehrhardt (1971) | 2 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ingels et al. (2003) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Latham (1790) | 2 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Potin (2013) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Probst (1997) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Purenne (2016) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 2 | 1,82% |
| Salomonsen (1934) | 2 | 0,79% | 2 | 1,52% | 0 | 0% | 2 | 1,82% |
| Uicn et al. (2015) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 1 | 0,91% |
| Weimerskirch et al. (2009) | 2 | 0,79% | 2 | 1,52% | 2 | 2,25% | 0 | 0% |
| Ahmed (2011) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Allen et al. (1876) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Anonyme. (2012) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Barré & Géraux (2004) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Bassin (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Bénito-espinal (1990) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Benson et al. (1975) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Benson (1967) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Birdlife International (2017) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Blyth (1860) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boddaert & Daubenton (1783) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruch (1832) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Cheke & Hume (2008) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| CHN (2017) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Clergeau & Pascal (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Collier et al. (2002) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Corre & Jouventin (1997) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Deblock (1966) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Deblock (1966) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Debout (2017) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Deflandre (2007) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deniau & Provost (2020) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Dufour & Veyrunes (2019) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Flitti & Rocha (2014) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Furminieux (2019) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Gould (1838) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Gray (1831) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guth (1971) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Hartert (1914) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Heller & Snodgrass (1901) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huey (1927) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Hunault & Kerbiriou (2007) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Hunault (2010) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Impact-mer (2011) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Jeanne et al. (2018) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Karadjian et al. (2022) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Lacan & Mougin (1974) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Corre (1996) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Leblond (2003) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Legros & Puissauve (2015) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Legros & Puissauve (2015) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Levesque & Delcroix (2013) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Lichtenstein (1823) | 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 et al. (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Lorvelec et al. (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Louette & Cousin (1999) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loury & Puissauve (2016) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Marion & Clergeau (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Marion & Clergeau (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Marion & Clergeau (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Marion & Marion (1982) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Marion (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Marion (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Marion (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Milne Edwards & Grandidier (1879) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Milne-edwards (1882) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Mourer-Chauvire et al. (1999) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olson & Warheit (1988) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Pallas (1773) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Payraudeau (1826) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2016) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Pratt (2011) | 1 | 0,4% | 1 | 0,76% | 0 | 0% | 1 | 0,91% |
| Puissauve (2016) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Ridgway (1893) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rothschild (1902) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Scopoli (1769) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Seguin et al. (2019) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Seriot et al. (1988) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Siorat & Rocamora (1995) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Siorat et al. (2003) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Spiroux (1996) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Temminck (1818-1838) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Trotignon (2022) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| UNEP-WCMC (2005) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Vanderwerf et al. (2006) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 0 | 0% |
| Vigors & Children (1826) | 1 | 0,4% | 1 | 0,76% | 1 | 1,12% | 1 | 0,91% |
| Wagler (1827) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli (2021) | 1 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
