Oiseaux nicheurs de France métropolitaine
641 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) | 180 | 21,05% | 58 | 18,83% | 58 | 19,14% | 56 | 18,48% |
Levesque & Delcroix (2018) | 44 | 5,15% | 43 | 13,96% | 43 | 14,19% | 43 | 14,19% |
Uicn et al. (2017) | 33 | 3,86% | 31 | 10,06% | 31 | 10,23% | 29 | 9,57% |
Etcheberry & Abraham (2009) | 31 | 3,63% | 26 | 8,44% | 26 | 8,58% | 26 | 8,58% |
UICN Comité français, OFB & MNHN (2021) | 30 | 3,51% | 30 | 9,74% | 30 | 9,9% | 29 | 9,57% |
Uicn et al. (2015) | 27 | 3,16% | 27 | 8,77% | 27 | 8,91% | 27 | 8,91% |
Linnaeus (1766) | 22 | 2,57% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Furminieux (2019) | 20 | 2,34% | 20 | 6,49% | 20 | 6,6% | 20 | 6,6% |
Questel (2020) | 19 | 2,22% | 19 | 6,17% | 19 | 6,27% | 19 | 6,27% |
Uicn et al. (2020) | 19 | 2,22% | 19 | 6,17% | 19 | 6,27% | 18 | 5,94% |
Yokoyama (2013) | 19 | 2,22% | 18 | 5,84% | 18 | 5,94% | 18 | 5,94% |
Karadjian et al. (2022) | 18 | 2,11% | 18 | 5,84% | 18 | 5,94% | 17 | 5,61% |
Questel & Le Quellec (2012) | 17 | 1,99% | 16 | 5,19% | 16 | 5,28% | 16 | 5,28% |
Remsen et al. (2013) | 17 | 1,99% | 17 | 5,52% | 17 | 5,61% | 15 | 4,95% |
Clements (2012) | 13 | 1,52% | 12 | 3,9% | 12 | 3,96% | 12 | 3,96% |
Joyeux & Baer (1955) | 13 | 1,52% | 8 | 2,6% | 8 | 2,64% | 7 | 2,31% |
Belfan & Conde (2016) | 12 | 1,4% | 12 | 3,9% | 12 | 3,96% | 12 | 3,96% |
Tostain et al. (2013) | 12 | 1,4% | 10 | 3,25% | 10 | 3,3% | 10 | 3,3% |
Barau et al. (2005) | 11 | 1,29% | 9 | 2,92% | 9 | 2,97% | 9 | 2,97% |
Rocamora (2004) | 10 | 1,17% | 8 | 2,6% | 8 | 2,64% | 8 | 2,64% |
Brehm (1831) | 9 | 1,05% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Gmelin (1789) | 9 | 1,05% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Scopoli (1769) | 9 | 1,05% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Weimerskirch et al. (2009) | 9 | 1,05% | 7 | 2,27% | 7 | 2,31% | 7 | 2,31% |
Deblock et al. (1960) | 8 | 0,94% | 5 | 1,62% | 5 | 1,65% | 5 | 1,65% |
Temminck et al. (1820-1840) | 7 | 0,82% | 4 | 1,3% | 4 | 1,32% | 4 | 1,32% |
Del Hoyo & Collar (2014) | 6 | 0,7% | 5 | 1,62% | 5 | 1,65% | 5 | 1,65% |
pallas (1764) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 5 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
Dickinson & Christidis (2014) | 5 | 0,58% | 5 | 1,62% | 5 | 1,65% | 5 | 1,65% |
Louette & Cousin (1999) | 5 | 0,58% | 5 | 1,62% | 5 | 1,65% | 5 | 1,65% |
Denis (2011) | 4 | 0,47% | 4 | 1,3% | 4 | 1,32% | 4 | 1,32% |
Gmelin (1788) | 4 | 0,47% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gonzalez et al. (2009) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 4 | 0,47% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lefranc & Issa (2013) | 4 | 0,47% | 4 | 1,3% | 4 | 1,32% | 4 | 1,32% |
Pontoppidan (1763) | 4 | 0,47% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Probst (1997) | 4 | 0,47% | 3 | 0,97% | 3 | 0,99% | 2 | 0,66% |
Schiebel (1910) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Socolovschi et al. (2012) | 4 | 0,47% | 4 | 1,3% | 4 | 1,32% | 4 | 1,32% |
Temminck et al. (1838) | 4 | 0,47% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Uicn et al. (2015) | 4 | 0,47% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Broyer (2009) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Bussiere & Labrousse (2015) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Cadiou et al. (2010) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Clements et al. (2015) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Durant et al. (2013) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Faggio et al. (2022) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Gargominy et al. (1996) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Gayet et al. (2010) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Genard & Lescourret (1987) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Guth (1971) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Kayser et al. (2019) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Latham (1790) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Moneglia et al. (2009) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Potin (2013) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Sharpe (1894) | 3 | 0,35% | 3 | 0,97% | 3 | 0,99% | 3 | 0,99% |
Une et al. (1817) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Arroyo et al. (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Bargain & Henry (2000) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Barre et al. (2009) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Beaubrun (2004) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Bechstein (1803) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Blumenbach (1810) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bortolato (1988) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudarel & Scher (2022) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Brambilla et al. (2008) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Burger et al. (2013) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Chappuis et al. (1974) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Chartier et al. (2007) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Chartier (1989) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Combrisson (1999) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Cosson et al. (1994) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Crouzier (2017) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
dal Molin (2009) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
D'Amico (2001) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Daniel et al. (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Davant (1967) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Debout (2001) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Debout (2004) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Delalande (1994) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Desfontaines (1787) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Dickinson & Remsen (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Dorleans (2022) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Dronneau & Wassmer (2008) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Dubois & Cugnasse (2015) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Dubois et al. (2008) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Duquet (2012) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Fontanilles et al. (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Formon (1975) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Frolet (2003) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Garoche & Sohier (2002) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Garoche & Sohier (2008) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Garoche & Sohier (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Genero (1987) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Gill (1995) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Gmelin (1770) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1774) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Grange et al. (2015) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Isenmann et al. (2000) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Jouard (1929) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouard (1929) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayser & Wilhelm (1991) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Kerbiriou et al. (2004) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Kerbiriou et al. (2006) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Knox et al. (2002) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Labitte (1955) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Lack & Lack (1951) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Lang (2010) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Latham (1787) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Leboulenger (1989) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Lepechin (1769) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesaffre (2009) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Levesque & Clergeau (2002) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Linnaeus (1761) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lovaty (2002) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Martinet et al. (1765) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Mays et al. (2006) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Morscheidt (1994) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Nipkow (1990) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Pallas (1769) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pallas (1831) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Paul & Lefranc (2011) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Pons et al. (2005) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Purenne (2016) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Safford & Hawkins (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Sangster et al. (2016) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Scopoli (1786) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Theuerkauf et al. (2010) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Thibault et al. (1987) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Thibault et al. (2014) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Thibault et al. (2023) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Tremauville (1991) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Tremblay et al. (2004) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Trotignon et al. (1994) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Tunstall (1880) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
UNEP-WCMC (2005) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Verbeek (1984) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Villard et al. (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Wolff et al. (2012) | 2 | 0,23% | 2 | 0,65% | 2 | 0,66% | 2 | 0,66% |
Zilli (2021) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Acerbi (1827) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Albesa (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2002) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2004) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2008) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
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Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
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Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
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Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
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Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
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Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
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Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Arthur et al. (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Attie & Jolivet (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Ausilio & Zotier (1989) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Baccetti et al. (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Balouet & Olson (1989) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Barré & Géraux (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Bassin (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Beaufils & Lecocq (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Bechstein (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beslot (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Birdlife International (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Bocher et al. (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Boet (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Boie (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaccorsi (2000) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Boschert & Dronneau (1998) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Bouzendorf & Guilpain (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Brehm (1820) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Brehm (1856) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Brème (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunet (2022) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Brünnich (1764) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Calenge et al. (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Cantera (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Catil (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chartier (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Chastel et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
CHN (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Christidis & Boles (2008) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Claessens (1992) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clech (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Lorvelec (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Vigne (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Vigne (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau & Vigne (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Coatmeur (1999) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Collette (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Comolet-Tirman et al. (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Constantin et al. (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Cormier (1984) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Coton et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Coton et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Csabaï (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
David et al. (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Deblock & Rose (1964) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Deboulonne (2014) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Debout & Desmares (1996) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Debout (1992) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Debout (1999) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Debout (2009) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Debout (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Deflandre (1999) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Deflandre (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Delacour (1963) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Desbrosses (1999) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Deutsche & Ornithologen-gesellschaft (1887) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dewynter & Claessens (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Bulletin de la Société zooogique de France, 26: 113.">D'hHmonville (1901) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
D'loia & D'Aloia (2014) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dubois et al. (2000) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Duquet (1996) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Efe et al. (2009) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Elfstrom (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Fijen (2014) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Fonteneau et al. (2018) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Fremaux & Petit (1998) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gallardo & Penteriani (2002) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gallien (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Genot et al. (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gibson & Baker (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gilot & Rousseau (2008) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gmelin (1791) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Godet et al. (2021) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gould (1837) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffith et al. (1829) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Güldenstädt (1770) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Guy et al. (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Hartert (1896) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hennique et al. (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Herman (1976) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Hermann (1804) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Homeyer (1853) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hunault & Kerbiriou (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Hunault (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Impact-mer (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Issa & Muller (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Keith & Cense (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Kempen van (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Labouyrie & Lacassin (2022) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lang & Lecocq (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Leblanc et al. (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Ledreff & Raynaud (1993) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Legros & Puissauve (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lethuillier (1999) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Levesque & Delcroix (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lichtenstein (1823) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Loison (1989) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec & Clergeau (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec & Vigne (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lorvelec et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Loury & Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lovaty (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Magaud & D'aubusson (1906) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Maksimova (1976) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion & Marion (1982) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Marion (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marion (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisner (1804) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Melin & Pascal (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Melin et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Michelat (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Montagu (1798) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Montin (1776) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1968) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Moreau (1990) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Moreau (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Nadal & Tariel (2008) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Naumann (1819) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Naumann (1840) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Noel et al. (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pallas (1773) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Parkin et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal & Clergeau (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pascal et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Payraudeau (1826) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pearson & Prévot (1971) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pereira et al. (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pilard et al. (2021) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pilard (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Poirel (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Poirier (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Poisson (1925) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Potapov (2005) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Poudré et al. (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pražák (1897) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Prevot (1971) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Puissauve & Legros (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Puissauve (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Quelennec (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Raspail (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Robert et al. (2002) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
ROGEON & SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
ROGEON & SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
ROGEON & SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Rothschild & Hartert (1910) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rufer & Malvesy (2009) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Cormoran, 15(4): 218.">Rundle & Rundle (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Sanchez et al. (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Sangster et al. (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Schiebel (1911) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (1870) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Siorat et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Siorat et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
SORDELLO (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Spanneut (1996) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Spiroux (1996) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Sueur et al. (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Taberlet (1983) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Temminck et al. ([1820-1840]) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2000) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Thibault et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Thibault (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Timon-David (1953) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Töpfer (2006) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Tostain & Dujardin (1988) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Tostain (1980) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Tresset et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Triplet et al. (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Trotignon (2022) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
UICN France, MNHN, LPO, SEOF & ONCFS. (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Une et al. (1816) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanardois (1977) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Verreaux & Des Murs (1860) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Vieillot (1819) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1823[1822]) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Viganò & Corso (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Vittorio et al. (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Voisin & Voisin (2001) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Voous (1949) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vorimore et al. (2021) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Wahl & Barbraud (2005) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Wells & Inskipp (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Yésou (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Zink et al. (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |