Pélécaniformes
Pelecaniformes
147 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 | 14,73% | 38 | 28,36% | 31 | 34,44% | 26 | 23,42% |
Levesque & Delcroix (2018) | 23 | 8,91% | 23 | 17,16% | 16 | 17,78% | 16 | 14,41% |
Remsen et al. (2013) | 23 | 8,91% | 23 | 17,16% | 23 | 25,56% | 13 | 11,71% |
Linnaeus (1758) | 22 | 8,53% | 7 | 5,22% | 7 | 7,78% | 4 | 3,6% |
Gmelin (1789) | 21 | 8,14% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
UICN Comité français, OFB & MNHN (2021) | 20 | 7,75% | 20 | 14,93% | 20 | 22,22% | 7 | 6,31% |
Uicn et al. (2015) | 17 | 6,59% | 17 | 12,69% | 17 | 18,89% | 7 | 6,31% |
Questel & Le Quellec (2012) | 15 | 5,81% | 15 | 11,19% | 12 | 13,33% | 8 | 7,21% |
Questel (2020) | 14 | 5,43% | 14 | 10,45% | 10 | 11,11% | 9 | 8,11% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 13 | 5,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 13 | 5,04% | 13 | 9,7% | 12 | 13,33% | 3 | 2,7% |
Belfan & Conde (2016) | 11 | 4,26% | 11 | 8,21% | 6 | 6,67% | 8 | 7,21% |
Weimerskirch et al. (2009) | 11 | 4,26% | 10 | 7,46% | 9 | 10% | 3 | 2,7% |
Rocamora (2004) | 10 | 3,88% | 9 | 6,72% | 7 | 7,78% | 5 | 4,5% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 9 | 3,49% | 9 | 6,72% | 7 | 7,78% | 7 | 6,31% |
Linnaeus (1766) | 8 | 3,1% | 4 | 2,99% | 3 | 3,33% | 3 | 2,7% |
Clements et al. (2015) | 7 | 2,71% | 7 | 5,22% | 3 | 3,33% | 6 | 5,41% |
Clements (2012) | 7 | 2,71% | 7 | 5,22% | 3 | 3,33% | 6 | 5,41% |
Dickinson & Remsen (2013) | 6 | 2,33% | 6 | 4,48% | 1 | 1,11% | 6 | 5,41% |
Tostain et al. (2013) | 6 | 2,33% | 6 | 4,48% | 6 | 6,67% | 4 | 3,6% |
Uicn et al. (2020) | 6 | 2,33% | 6 | 4,48% | 6 | 6,67% | 3 | 2,7% |
Gill (1995) | 5 | 1,94% | 5 | 3,73% | 5 | 5,56% | 0 | 0% |
Safford & Hawkins (2013) | 5 | 1,94% | 5 | 3,73% | 2 | 2,22% | 3 | 2,7% |
Barau et al. (2005) | 4 | 1,55% | 4 | 2,99% | 3 | 3,33% | 1 | 0,9% |
Dubois et al. (2008) | 4 | 1,55% | 4 | 2,99% | 4 | 4,44% | 4 | 3,6% |
Thibault et al. (2014) | 4 | 1,55% | 4 | 2,99% | 4 | 4,44% | 1 | 0,9% |
Commission de l’Avifaune Française (2016) | 3 | 1,16% | 3 | 2,24% | 3 | 3,33% | 0 | 0% |
Dodson & Fitzgerald (1980) | 3 | 1,16% | 2 | 1,49% | 0 | 0% | 2 | 1,8% |
Etcheberry & Abraham (2009) | 3 | 1,16% | 3 | 2,24% | 3 | 3,33% | 1 | 0,9% |
Lesson (1831) | 3 | 1,16% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Mathews (1914) | 3 | 1,16% | 2 | 1,49% | 1 | 1,11% | 2 | 1,8% |
Barre et al. (2009) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
Blumenbach (1810) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosc (1792) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Chartier et al. (2007) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 0 | 0% |
Commecy et al. (2013) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
Cowles (1994) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Daniel et al. (2020) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 0 | 0% |
Ehrhardt (1971) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels et al. (2003) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
Latham (1790) | 2 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Potin (2013) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
Probst (1997) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 1 | 0,9% |
Purenne (2016) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 2 | 1,8% |
Salomonsen (1934) | 2 | 0,78% | 2 | 1,49% | 0 | 0% | 2 | 1,8% |
Tatin et al. (2003) | 2 | 0,78% | 2 | 1,49% | 0 | 0% | 2 | 1,8% |
Uicn et al. (2015) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 1 | 0,9% |
Weimerskirch et al. (2009) | 2 | 0,78% | 2 | 1,49% | 2 | 2,22% | 0 | 0% |
Ahmed (2011) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Allen et al. (1876) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Anonyme. (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Barbraud (2012) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Barré & Géraux (2004) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Bassin (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Bénito-espinal (1990) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Benson et al. (1975) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Benson (1967) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Birdlife International (2017) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Blyth (1860) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruch (1832) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Cheke & Hume (2008) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
CHN (2017) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Clement & Chapalain (2016) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Clergeau & Pascal (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Collier et al. (2002) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Corre & Jouventin (1997) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Deblock (1966) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Deblock (1966) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Debout (2017) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Deflandre (2007) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Deniau & Provost (2020) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Dufour & Veyrunes (2019) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Flitti & Rocha (2014) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Furminieux (2019) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Gould (1838) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Gray (1831) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Guth (1971) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Hartert (1914) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Heller & Snodgrass (1901) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Huey (1927) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Hunault & Kerbiriou (2007) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Hunault (2010) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Impact-mer (2011) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Jeanne et al. (2018) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Karadjian et al. (2022) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Lacan & Mougin (1974) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre (1996) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Leblond (2003) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Legros & Puissauve (2015) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Legros & Puissauve (2015) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Levesque & Delcroix (2013) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Lichtenstein (1823) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Lorvelec et al. (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Louette & Cousin (1999) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Loury & Puissauve (2016) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Marion & Clergeau (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Marion & Clergeau (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Marion & Clergeau (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Marion (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Marion (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Marion (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Milne Edwards & Grandidier (1879) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Milne-edwards (1882) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Mourer-Chauvire et al. (1999) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Olson & Warheit (1988) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Pallas (1773) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Payraudeau (1826) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2016) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Pratt (2011) | 1 | 0,39% | 1 | 0,75% | 0 | 0% | 1 | 0,9% |
Puissauve (2016) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Ridgway (1893) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Rothschild (1902) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Scopoli (1769) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Seguin et al. (2019) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Seriot et al. (1988) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Siorat & Rocamora (1995) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Siorat et al. (2003) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Spiroux (1996) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Temminck (1818-1838) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Trotignon (2022) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
UNEP-WCMC (2005) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Vanderwerf et al. (2006) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 0 | 0% |
Vigors & Children (1826) | 1 | 0,39% | 1 | 0,75% | 1 | 1,11% | 1 | 0,9% |
Wagler (1827) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |