Limicoles
Charadrii et Scolopaci
146 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) | 49 | 15,76% | 47 | 33,81% | 37 | 33,33% | 37 | 30,33% |
Levesque & Delcroix (2018) | 48 | 15,43% | 47 | 33,81% | 41 | 36,94% | 42 | 34,43% |
Linnaeus (1758) | 33 | 10,61% | 8 | 5,76% | 8 | 7,21% | 6 | 4,92% |
UICN Comité français, OFB & MNHN (2021) | 32 | 10,29% | 32 | 23,02% | 32 | 28,83% | 24 | 19,67% |
Etcheberry & Abraham (2009) | 29 | 9,32% | 28 | 20,14% | 28 | 25,23% | 21 | 17,21% |
Questel (2020) | 29 | 9,32% | 28 | 20,14% | 26 | 23,42% | 23 | 18,85% |
Yokoyama (2013) | 29 | 9,32% | 26 | 18,71% | 26 | 23,42% | 21 | 17,21% |
Dewynter (2021) | 27 | 8,68% | 27 | 19,42% | 26 | 23,42% | 22 | 18,03% |
Remsen et al. (2013) | 26 | 8,36% | 25 | 17,99% | 25 | 22,52% | 19 | 15,57% |
Uicn et al. (2015) | 25 | 8,04% | 25 | 17,99% | 25 | 22,52% | 17 | 13,93% |
Belfan & Conde (2016) | 24 | 7,72% | 23 | 16,55% | 22 | 19,82% | 20 | 16,39% |
Questel & Le Quellec (2012) | 22 | 7,07% | 22 | 15,83% | 20 | 18,02% | 19 | 15,57% |
Deblock et al. (1960) | 14 | 4,5% | 8 | 5,76% | 8 | 7,21% | 5 | 4,1% |
Rocamora (2004) | 14 | 4,5% | 13 | 9,35% | 13 | 11,71% | 10 | 8,2% |
Barau et al. (2005) | 12 | 3,86% | 10 | 7,19% | 10 | 9,01% | 7 | 5,74% |
Clements (2012) | 11 | 3,54% | 11 | 7,91% | 6 | 5,41% | 6 | 4,92% |
Gmelin (1789) | 10 | 3,22% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Tostain et al. (2013) | 9 | 2,89% | 8 | 5,76% | 8 | 7,21% | 5 | 4,1% |
Uicn et al. (2015) | 9 | 2,89% | 8 | 5,76% | 8 | 7,21% | 6 | 4,92% |
Thibault et al. (2014) | 8 | 2,57% | 7 | 5,04% | 6 | 5,41% | 4 | 3,28% |
Uicn et al. (2020) | 7 | 2,25% | 7 | 5,04% | 7 | 6,31% | 6 | 4,92% |
Ausilio & Zotier (1989) | 6 | 1,93% | 6 | 4,32% | 6 | 5,41% | 5 | 4,1% |
Del Hoyo & Collar (2014) | 6 | 1,93% | 5 | 3,6% | 4 | 3,6% | 5 | 4,1% |
Dickinson & Remsen (2013) | 6 | 1,93% | 5 | 3,6% | 1 | 0,9% | 4 | 3,28% |
Gill (1995) | 6 | 1,93% | 6 | 4,32% | 6 | 5,41% | 3 | 2,46% |
Weimerskirch et al. (2009) | 6 | 1,93% | 6 | 4,32% | 6 | 5,41% | 4 | 3,28% |
Dubois et al. (2008) | 5 | 1,61% | 5 | 3,6% | 5 | 4,5% | 3 | 2,46% |
Louette & Cousin (1999) | 4 | 1,29% | 4 | 2,88% | 4 | 3,6% | 4 | 3,28% |
Vieillot (1819) | 4 | 1,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1831) | 3 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Commission de l’Avifaune Française (2016) | 3 | 0,96% | 3 | 2,16% | 3 | 2,7% | 3 | 2,46% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels et al. (2003) | 3 | 0,96% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Linnaeus (1766) | 3 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1764) | 2 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Amico (2001) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Ehrhardt (1971) | 2 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Guth (1971) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 1 | 0,82% |
Jansen et al. (2021) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Leisler (1812-1813) | 2 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Delcroix (2016) | 2 | 0,64% | 1 | 0,72% | 0 | 0% | 1 | 0,82% |
Nipkow (1990) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
pallas (1764) | 2 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 2 | 0,64% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Pontoppidan (1763) | 2 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharpe (1906) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Temminck et al. (1838) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Tostain (1980) | 2 | 0,64% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Walters (1991) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Wilson (1813) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 0 | 0% |
Wilson-aggarwal et al. (2016) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Worthy et al. (2013) | 2 | 0,64% | 2 | 1,44% | 2 | 1,8% | 2 | 1,64% |
Anonyme (2008) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Baker et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Barre (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,32% | 1 | 0,72% | 0 | 0% | 1 | 0,82% |
Beaufils (1999) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Bechstein (1803) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2016) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Blanvillain et al. (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Bocher et al. (2013) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Boddaert & Daubenton (1783) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Bougeard & Siblet (2000) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
CHN (2017) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Clements et al. (2015) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Clements (1992) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Clergeau & Pascal (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Clergeau & Pascal (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Clergeau et al. (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Coues (1861) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Crouzier (2009) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Cudo (1995) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock & Rose (1964) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Debout (2009) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Dubois & Louvet (2014) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Ferrand et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Fonteneau et al. (2018) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Fremont (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Gunnerus (1767) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-mer (2011) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
IUCN (2014) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Jiguet (2023) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Kayser & Wilhelm (1991) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Latham (1787) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Leblanc et al. (2020) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Linnaeus (1767) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Loury & Puissauve (2016) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Loury & Puissauve (2016) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Martinet et al. (1765) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Mctavish (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Morrison (2006) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Olioso (1996) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (2000) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Pallas (1771) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1773) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Pascal & Clergeau (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Pascal et al. (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 0 | 0% |
Pinchon (1976) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Potin (2013) | 1 | 0,32% | 1 | 0,72% | 0 | 0% | 1 | 0,82% |
Reeber (2015) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Safford & Hawkins (2013) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Scopoli (1786) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Sueur et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Sueur (2018) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Trevoux (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Uicn et al. (2011) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Vieillot (1817) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Vieillot (1818) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |
Vieillot (1819) | 1 | 0,32% | 1 | 0,72% | 1 | 0,9% | 1 | 0,82% |