Limicoles
Charadrii et Scolopaci
155 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 | 15,51% | 47 | 33,81% | 37 | 33,04% | 37 | 30,08% |
| Levesque & Delcroix (2018) | 48 | 15,19% | 47 | 33,81% | 41 | 36,61% | 42 | 34,15% |
| Linnaeus (1758) | 33 | 10,44% | 8 | 5,76% | 8 | 7,14% | 6 | 4,88% |
| UICN Comité français, OFB & MNHN (2021) | 32 | 10,13% | 32 | 23,02% | 32 | 28,57% | 24 | 19,51% |
| Etcheberry & Abraham (2009) | 29 | 9,18% | 28 | 20,14% | 28 | 25% | 22 | 17,89% |
| Questel (2020) | 29 | 9,18% | 28 | 20,14% | 26 | 23,21% | 23 | 18,7% |
| Yokoyama (2013) | 29 | 9,18% | 26 | 18,71% | 26 | 23,21% | 21 | 17,07% |
| Dewynter (2021) | 27 | 8,54% | 27 | 19,42% | 26 | 23,21% | 22 | 17,89% |
| Remsen et al. (2013) | 26 | 8,23% | 25 | 17,99% | 25 | 22,32% | 19 | 15,45% |
| Uicn et al. (2015) | 25 | 7,91% | 25 | 17,99% | 25 | 22,32% | 17 | 13,82% |
| Belfan & Conde (2016) | 24 | 7,59% | 23 | 16,55% | 22 | 19,64% | 20 | 16,26% |
| Questel & Le Quellec (2012) | 22 | 6,96% | 22 | 15,83% | 20 | 17,86% | 19 | 15,45% |
| Deblock et al. (1960) | 14 | 4,43% | 8 | 5,76% | 8 | 7,14% | 5 | 4,07% |
| Rocamora (2004) | 14 | 4,43% | 13 | 9,35% | 13 | 11,61% | 10 | 8,13% |
| Barau et al. (2005) | 12 | 3,8% | 10 | 7,19% | 10 | 8,93% | 7 | 5,69% |
| Clements (2012) | 11 | 3,48% | 11 | 7,91% | 6 | 5,36% | 6 | 4,88% |
| Gmelin (1789) | 10 | 3,16% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Tostain et al. (2013) | 9 | 2,85% | 8 | 5,76% | 8 | 7,14% | 5 | 4,07% |
| Uicn et al. (2015) | 9 | 2,85% | 8 | 5,76% | 8 | 7,14% | 6 | 4,88% |
| Thibault et al. (2014) | 8 | 2,53% | 7 | 5,04% | 6 | 5,36% | 4 | 3,25% |
| Uicn et al. (2020) | 7 | 2,22% | 7 | 5,04% | 7 | 6,25% | 6 | 4,88% |
| Ausilio & Zotier (1989) | 6 | 1,9% | 6 | 4,32% | 6 | 5,36% | 5 | 4,07% |
| Del Hoyo & Collar (2014) | 6 | 1,9% | 5 | 3,6% | 4 | 3,57% | 5 | 4,07% |
| Dickinson & Remsen (2013) | 6 | 1,9% | 5 | 3,6% | 1 | 0,89% | 4 | 3,25% |
| Gill (1995) | 6 | 1,9% | 6 | 4,32% | 6 | 5,36% | 3 | 2,44% |
| Weimerskirch et al. (2009) | 6 | 1,9% | 6 | 4,32% | 6 | 5,36% | 4 | 3,25% |
| Bartoli (1972) | 5 | 1,58% | 5 | 3,6% | 5 | 4,46% | 4 | 3,25% |
| Dubois et al. (2008) | 5 | 1,58% | 5 | 3,6% | 5 | 4,46% | 3 | 2,44% |
| Louette & Cousin (1999) | 4 | 1,27% | 4 | 2,88% | 4 | 3,57% | 4 | 3,25% |
| Vieillot (1819) | 4 | 1,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brehm (1831) | 3 | 0,95% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Commission de l’Avifaune Française (2016) | 3 | 0,95% | 3 | 2,16% | 3 | 2,68% | 3 | 2,44% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,95% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ingels et al. (2003) | 3 | 0,95% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Linnaeus (1766) | 3 | 0,95% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1764) | 2 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'Amico (2001) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Ehrhardt (1971) | 2 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson & Baker (2012) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Guth (1971) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Jansen et al. (2021) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Lapous (1988) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Leisler (1812-1813) | 2 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Delcroix (2016) | 2 | 0,63% | 1 | 0,72% | 0 | 0% | 1 | 0,81% |
| Nipkow (1990) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| pallas (1764) | 2 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 2 | 0,63% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Pontoppidan (1763) | 2 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sharpe (1906) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Temminck et al. (1838) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Tostain (1980) | 2 | 0,63% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Walters (1991) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Wilson (1813) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 0 | 0% |
| Wilson-aggarwal et al. (2016) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Worthy et al. (2013) | 2 | 0,63% | 2 | 1,44% | 2 | 1,79% | 2 | 1,63% |
| Anonyme (2008) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Anonyme. (2012) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Baker et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Barre (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Bauer et al. (2010) | 1 | 0,32% | 1 | 0,72% | 0 | 0% | 1 | 0,81% |
| Beaufils (1999) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Bechstein (1803) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Birdlife International (2016) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Blanvillain et al. (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Bocher et al. (2013) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Boddaert & Daubenton (1783) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bougeard & Siblet (2000) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| CHN (2017) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Clements et al. (2015) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Clements (1992) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Clergeau & Pascal (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Clergeau & Pascal (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Clergeau et al. (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Coues (1861) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crepeau (1973) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Crouzier (2009) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Cudo (1995) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deblock & Rose (1964) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Debout (2009) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Dollfus (1966) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois & Louvet (2014) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Ferrand et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Fonteneau et al. (2018) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Fremont (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Gunnerus (1767) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-mer (2011) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| IUCN (2014) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Jiguet (2023) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Johnson (1973) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kayser & Wilhelm (1991) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Latham (1787) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leblanc et al. (2020) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| 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 | 0,89% | 1 | 0,81% |
| Loury & Puissauve (2016) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Maout (2019) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Martinet et al. (1765) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mctavish (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Morrison (2006) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Olioso (1996) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivier (2000) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Pallas (1771) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1773) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Pascal & Clergeau (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Pascal et al. (2003) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 0 | 0% |
| Pinchon (1976) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Potin (2013) | 1 | 0,32% | 1 | 0,72% | 0 | 0% | 1 | 0,81% |
| Raitiere et al. (2013) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Reeber (2015) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Safford & Hawkins (2013) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Sane (2004) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Scopoli (1786) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Sueur et al. (2007) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Sueur (2018) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Trevoux (2002) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Uicn et al. (2011) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Vieillot (1817) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Vieillot (1818) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
| Vieillot (1819) | 1 | 0,32% | 1 | 0,72% | 1 | 0,89% | 1 | 0,81% |
