Hérons, cigognes, spatules, ibis, flamants et grues
111 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) | 32 | 17,39% | 32 | 34,41% | 25 | 35,21% | 24 | 30% |
Linnaeus (1758) | 24 | 13,04% | 7 | 7,53% | 7 | 9,86% | 5 | 6,25% |
Remsen et al. (2013) | 19 | 10,33% | 19 | 20,43% | 19 | 26,76% | 11 | 13,75% |
Levesque & Delcroix (2018) | 17 | 9,24% | 17 | 18,28% | 11 | 15,49% | 14 | 17,5% |
Gmelin (1789) | 16 | 8,7% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 16 | 8,7% | 16 | 17,2% | 16 | 22,54% | 8 | 10% |
Belfan & Conde (2016) | 11 | 5,98% | 11 | 11,83% | 6 | 8,45% | 8 | 10% |
Questel (2020) | 11 | 5,98% | 11 | 11,83% | 9 | 12,68% | 6 | 7,5% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 10 | 5,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 10 | 5,43% | 10 | 10,75% | 7 | 9,86% | 7 | 8,75% |
Clements (2012) | 9 | 4,89% | 9 | 9,68% | 6 | 8,45% | 9 | 11,25% |
Yokoyama (2013) | 9 | 4,89% | 9 | 9,68% | 9 | 12,68% | 2 | 2,5% |
Dickinson & Remsen (2013) | 8 | 4,35% | 8 | 8,6% | 3 | 4,23% | 8 | 10% |
Rocamora (2004) | 7 | 3,8% | 6 | 6,45% | 4 | 5,63% | 6 | 7,5% |
Uicn et al. (2015) | 7 | 3,8% | 7 | 7,53% | 7 | 9,86% | 3 | 3,75% |
Uicn et al. (2020) | 6 | 3,26% | 6 | 6,45% | 6 | 8,45% | 4 | 5% |
Linnaeus (1766) | 5 | 2,72% | 2 | 2,15% | 2 | 2,82% | 2 | 2,5% |
Commecy et al. (2013) | 4 | 2,17% | 4 | 4,3% | 4 | 5,63% | 4 | 5% |
Dubois et al. (2008) | 4 | 2,17% | 4 | 4,3% | 4 | 5,63% | 4 | 5% |
Tostain et al. (2013) | 4 | 2,17% | 4 | 4,3% | 4 | 5,63% | 4 | 5% |
Weimerskirch et al. (2009) | 4 | 2,17% | 3 | 3,23% | 3 | 4,23% | 0 | 0% |
Barau et al. (2005) | 2 | 1,09% | 2 | 2,15% | 1 | 1,41% | 1 | 1,25% |
Bosc (1792) | 2 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Chartier et al. (2007) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 0 | 0% |
Commission de l’Avifaune Française (2016) | 2 | 1,09% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Cowles (1994) | 2 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Daniel et al. (2020) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 0 | 0% |
Etcheberry & Abraham (2009) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 0 | 0% |
Ingels et al. (2003) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 2 | 2,5% |
Latham (1790) | 2 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (1997) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 2 | 2,5% |
Purenne (2016) | 2 | 1,09% | 2 | 2,15% | 2 | 2,82% | 2 | 2,5% |
Safford & Hawkins (2013) | 2 | 1,09% | 2 | 2,15% | 1 | 1,41% | 1 | 1,25% |
Salomonsen (1934) | 2 | 1,09% | 2 | 2,15% | 0 | 0% | 2 | 2,5% |
Ahmed (2011) | 1 | 0,54% | 1 | 1,08% | 0 | 0% | 1 | 1,25% |
Allen et al. (1876) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Anonyme. (2012) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Barre et al. (2009) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Bassin (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Birdlife International (2017) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Boddaert & Daubenton (1783) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
CHN (2017) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Clements et al. (2015) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Clergeau & Johnson (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Clergeau & Pascal (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Deblock (1966) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Deflandre (2007) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2014) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Furminieux (2019) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Gill (1995) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Gould (1838) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Gray (1831) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Guth (1971) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Hartert (1914) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Huey (1927) | 1 | 0,54% | 1 | 1,08% | 0 | 0% | 1 | 1,25% |
Hunault & Kerbiriou (2007) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Hunault (2010) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Impact-mer (2011) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
IUCN (2013) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Jeanne et al. (2018) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Karadjian et al. (2022) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Kayser et al. (2019) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Legros & Puissauve (2015) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Legros & Puissauve (2015) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Lesson (1831) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Lorvelec et al. (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Loury & Puissauve (2016) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Marion & Clergeau (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Marion & Clergeau (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Marion & Clergeau (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Marion & Marion (1982) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Marion (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Marion (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Milne Edwards & Grandidier (1879) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Molina (1782) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Moreau (1990) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Mourer-Chauvire et al. (1999) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Pascal et al. (2003) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Pearman et al. (2016) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
Potin (2013) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Pratt (2011) | 1 | 0,54% | 1 | 1,08% | 0 | 0% | 1 | 1,25% |
Puissauve (2016) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Scopoli (1769) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Seguin et al. (2019) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Seriot et al. (1988) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Spiroux (1996) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Thibault et al. (2014) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Trotignon (2022) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Uicn et al. (2015) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 0 | 0% |
UNEP-WCMC (2005) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Vigors & Children (1826) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Vorimore et al. (2021) | 1 | 0,54% | 1 | 1,08% | 1 | 1,41% | 1 | 1,25% |
Wagler (1827) | 1 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |