Oiseaux marins de France métropolitaine
261 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) | 59 | 16,86% | 54 | 36,73% | 53 | 39,26% | 51 | 36,43% |
Levesque & Delcroix (2018) | 55 | 15,71% | 52 | 35,37% | 52 | 38,52% | 49 | 35% |
UICN Comité français, OFB & MNHN (2021) | 50 | 14,29% | 50 | 34,01% | 50 | 37,04% | 47 | 33,57% |
Linnaeus (1758) | 41 | 11,71% | 11 | 7,48% | 11 | 8,15% | 10 | 7,14% |
Etcheberry & Abraham (2009) | 38 | 10,86% | 34 | 23,13% | 34 | 25,19% | 34 | 24,29% |
Remsen et al. (2013) | 35 | 10% | 31 | 21,09% | 31 | 22,96% | 29 | 20,71% |
Yokoyama (2013) | 34 | 9,71% | 31 | 21,09% | 31 | 22,96% | 29 | 20,71% |
Uicn et al. (2015) | 31 | 8,86% | 29 | 19,73% | 29 | 21,48% | 29 | 20,71% |
Belfan & Conde (2016) | 28 | 8% | 23 | 15,65% | 23 | 17,04% | 23 | 16,43% |
Questel & Le Quellec (2012) | 28 | 8% | 27 | 18,37% | 27 | 20% | 25 | 17,86% |
Questel (2020) | 27 | 7,71% | 25 | 17,01% | 25 | 18,52% | 24 | 17,14% |
Clements (2012) | 18 | 5,14% | 17 | 11,56% | 17 | 12,59% | 13 | 9,29% |
Tostain et al. (2013) | 17 | 4,86% | 15 | 10,2% | 15 | 11,11% | 14 | 10% |
Uicn et al. (2015) | 15 | 4,29% | 13 | 8,84% | 13 | 9,63% | 13 | 9,29% |
Dewynter (2021) | 14 | 4% | 14 | 9,52% | 14 | 10,37% | 14 | 10% |
Deblock et al. (1960) | 11 | 3,14% | 4 | 2,72% | 4 | 2,96% | 4 | 2,86% |
Uicn et al. (2020) | 11 | 3,14% | 11 | 7,48% | 11 | 8,15% | 9 | 6,43% |
Barau et al. (2005) | 10 | 2,86% | 8 | 5,44% | 8 | 5,93% | 8 | 5,71% |
Dickinson & Remsen (2013) | 9 | 2,57% | 8 | 5,44% | 8 | 5,93% | 8 | 5,71% |
Weimerskirch et al. (2009) | 9 | 2,57% | 8 | 5,44% | 8 | 5,93% | 8 | 5,71% |
Del Hoyo & Collar (2014) | 8 | 2,29% | 7 | 4,76% | 4 | 2,96% | 7 | 5% |
Rocamora (2004) | 8 | 2,29% | 7 | 4,76% | 7 | 5,19% | 7 | 5% |
Gill (1995) | 6 | 1,71% | 6 | 4,08% | 6 | 4,44% | 6 | 4,29% |
Gmelin (1789) | 6 | 1,71% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Pontoppidan (1763) | 6 | 1,71% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Thibault et al. (2014) | 6 | 1,71% | 6 | 4,08% | 6 | 4,44% | 6 | 4,29% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 6 | 1,71% | 6 | 4,08% | 6 | 4,44% | 6 | 4,29% |
CHN (2017) | 5 | 1,43% | 5 | 3,4% | 5 | 3,7% | 5 | 3,57% |
Commecy et al. (2013) | 5 | 1,43% | 5 | 3,4% | 5 | 3,7% | 5 | 3,57% |
Furminieux (2019) | 5 | 1,43% | 5 | 3,4% | 5 | 3,7% | 4 | 2,86% |
Bartoli (1972) | 4 | 1,14% | 3 | 2,04% | 3 | 2,22% | 3 | 2,14% |
Commission de l’Avifaune Française (2016) | 4 | 1,14% | 4 | 2,72% | 4 | 2,96% | 4 | 2,86% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 1,14% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Karadjian et al. (2022) | 4 | 1,14% | 4 | 2,72% | 4 | 2,96% | 3 | 2,14% |
Linnaeus (1766) | 4 | 1,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 4 | 1,14% | 4 | 2,72% | 4 | 2,96% | 4 | 2,86% |
Temminck et al. (1838) | 4 | 1,14% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Vieillot (1819) | 4 | 1,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ausilio & Zotier (1989) | 3 | 0,86% | 3 | 2,04% | 3 | 2,22% | 3 | 2,14% |
Brünnich (1764) | 3 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Cadiou et al. (2010) | 3 | 0,86% | 3 | 2,04% | 3 | 2,22% | 0 | 0% |
Dubois et al. (2008) | 3 | 0,86% | 3 | 2,04% | 3 | 2,22% | 3 | 2,14% |
Faggio et al. (2022) | 3 | 0,86% | 3 | 2,04% | 3 | 2,22% | 3 | 2,14% |
Pallas (1831) | 3 | 0,86% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Pons et al. (2005) | 3 | 0,86% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Probst (1997) | 3 | 0,86% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Tostain & Dujardin (1988) | 3 | 0,86% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Tostain (1980) | 3 | 0,86% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Beaubrun (2004) | 2 | 0,57% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Blumenbach (1810) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Chappuis et al. (1974) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
dal Molin (2009) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Davant (1967) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois (2006) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Gibson & Baker (2012) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Gourreau et al. (1998) | 2 | 0,57% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Guiguen et al. (1984) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 1 | 0,71% |
Hervé & François (1995) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Jardine & Selby (1826-1835) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1801) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Lepechin (1769) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 2 | 0,57% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Linnaeus (1761) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Louette & Cousin (1999) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Martinet et al. (1765) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1914) | 2 | 0,57% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Mays et al. (2006) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
pallas (1764) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1773) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezy et al. (2022) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Sabine (1819) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Tatin et al. (2003) | 2 | 0,57% | 2 | 1,36% | 0 | 0% | 2 | 1,43% |
Trotignon et al. (1994) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Weimerskirch et al. (2009) | 2 | 0,57% | 2 | 1,36% | 2 | 1,48% | 2 | 1,43% |
Zilli (2021) | 2 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Acerbi (1827) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Anonyme. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Attié et al. (1997) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Austin et al. (2004) | 1 | 0,29% | 1 | 0,68% | 0 | 0% | 1 | 0,71% |
Barré & Géraux (2004) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Barre et al. (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Bartoli & Prévot (1986) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaufils (1999) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Bénito-espinal (1990) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Bertrand (1982) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Birdlife International (2016) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Boie (1835) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1857) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Boschert & Dronneau (1998) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Bougeard & Siblet (2000) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Bougeard (2007) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1831) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Brème (1839) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruch (1832) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Chastel et al. (1987) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Cheke & Hume (2008) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Clements et al. (2015) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Clergeau & Johnson (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Clergeau & Pascal (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Clergeau et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Clergeau et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Collier et al. (2002) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Contejean (2018) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Cory (1881) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Costrel & Corainville (1929) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Coues (1861) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Crouzier (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Deblock (1966) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Debout & Desmares (1996) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Debout (1992) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Debout (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Debout (2017) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Deniau & Provost (2020) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Dollfus (1966) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufour & Veyrunes (2019) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Efe et al. (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Flood et al. (2017) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Fonteneau et al. (2018) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Gallien (2011) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Gernigon & Lacaze (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Gernigon (2008) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1956) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1859) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Guermeur (1987) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1767) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Harcourt (1851) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Homeyer (1853) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-mer (2011) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Ingels et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
IUCN (2013) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
IUCN (2014) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Johnson (1973) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayser et al. (2019) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Kuhl (1820) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Leblanc et al. (2020) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Legros & Puissauve (2015) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Legros & Puissauve (2015) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Lesage et al. (2024) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Lesson (1839) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Lethuillier (1999) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Levesque & Delcroix (2016) | 1 | 0,29% | 1 | 0,68% | 0 | 0% | 1 | 0,71% |
Lichtenstein (1823) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1759) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Lorvelec et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Loury & Puissauve (2016) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Lowe (1920) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Macgillivray (1824) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Magaud & D'aubusson (1906) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Marion (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Mathews (1912) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-edwards (1882) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Molina (1782) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Montagu (1813) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Morrison (2006) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Naumann (1819) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Naumann (1840) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Nuttall (1834) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
O'reilly (1818) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Clergeau (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Payraudeau (1826) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearson & Prévot (1971) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Petit (1976) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Phipps (1774) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Plestan et al. (2009) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Prevot (1971) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Reeber et al. (1996) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeber (2015) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Roques (1991) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvadori (1899) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez et al. (2004) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Scopoli (1769) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Siorat et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Siorat et al. (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Sueur et al. (2007) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Temminck et al. ([1820-1840]) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Texier (1914) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Trevoux (2002) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Uicn et al. (2011) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Vanderwerf et al. (2004) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanderwerf et al. (2006) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Vieillot (1817) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincent (1990) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Vorimore et al. (2021) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yesou & Thebault (2012) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yésou (2003) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 0 | 0% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |
Yésou (2003) | 1 | 0,29% | 1 | 0,68% | 1 | 0,74% | 1 | 0,71% |