Oiseaux marins de Saint-Pierre-et-Miquelon
166 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Levesque & Delcroix (2018) | 53 | 24,09% | 51 | 59,3% | 51 | 59,3% | 51 | 59,3% |
| Uicn et al. (2017) | 49 | 22,27% | 45 | 52,33% | 45 | 52,33% | 45 | 52,33% |
| UICN Comité français, OFB & MNHN (2021) | 45 | 20,45% | 45 | 52,33% | 45 | 52,33% | 45 | 52,33% |
| Etcheberry & Abraham (2009) | 41 | 18,64% | 37 | 43,02% | 37 | 43,02% | 37 | 43,02% |
| Linnaeus (1758) | 34 | 15,45% | 6 | 6,98% | 6 | 6,98% | 6 | 6,98% |
| Remsen et al. (2013) | 31 | 14,09% | 28 | 32,56% | 28 | 32,56% | 28 | 32,56% |
| Belfan & Conde (2016) | 28 | 12,73% | 26 | 30,23% | 26 | 30,23% | 26 | 30,23% |
| Yokoyama (2013) | 28 | 12,73% | 25 | 29,07% | 25 | 29,07% | 25 | 29,07% |
| Questel (2020) | 26 | 11,82% | 24 | 27,91% | 24 | 27,91% | 24 | 27,91% |
| Questel & Le Quellec (2012) | 23 | 10,45% | 22 | 25,58% | 22 | 25,58% | 22 | 25,58% |
| Uicn et al. (2015) | 21 | 9,55% | 19 | 22,09% | 19 | 22,09% | 19 | 22,09% |
| Dewynter (2021) | 15 | 6,82% | 15 | 17,44% | 15 | 17,44% | 15 | 17,44% |
| Uicn et al. (2015) | 13 | 5,91% | 11 | 12,79% | 11 | 12,79% | 11 | 12,79% |
| Clements (2012) | 11 | 5% | 11 | 12,79% | 11 | 12,79% | 11 | 12,79% |
| Tostain et al. (2013) | 11 | 5% | 10 | 11,63% | 10 | 11,63% | 10 | 11,63% |
| Uicn et al. (2020) | 11 | 5% | 11 | 12,79% | 11 | 12,79% | 11 | 12,79% |
| Deblock et al. (1960) | 10 | 4,55% | 4 | 4,65% | 4 | 4,65% | 4 | 4,65% |
| Barau et al. (2005) | 7 | 3,18% | 7 | 8,14% | 7 | 8,14% | 7 | 8,14% |
| Pontoppidan (1763) | 5 | 2,27% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Rocamora (2004) | 5 | 2,27% | 5 | 5,81% | 5 | 5,81% | 5 | 5,81% |
| CHN (2017) | 4 | 1,82% | 4 | 4,65% | 4 | 4,65% | 4 | 4,65% |
| Del Hoyo & Collar (2014) | 4 | 1,82% | 3 | 3,49% | 3 | 3,49% | 3 | 3,49% |
| Dickinson & Remsen (2013) | 4 | 1,82% | 4 | 4,65% | 4 | 4,65% | 4 | 4,65% |
| Furminieux (2019) | 4 | 1,82% | 4 | 4,65% | 4 | 4,65% | 4 | 4,65% |
| Tostain & Dujardin (1988) | 4 | 1,82% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 4 | 1,82% | 4 | 4,65% | 4 | 4,65% | 4 | 4,65% |
| Vieillot (1819) | 4 | 1,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 4 | 1,82% | 3 | 3,49% | 3 | 3,49% | 3 | 3,49% |
| Ausilio & Zotier (1989) | 3 | 1,36% | 3 | 3,49% | 3 | 3,49% | 3 | 3,49% |
| Bartoli (1972) | 3 | 1,36% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Brünnich (1764) | 3 | 1,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karadjian et al. (2022) | 3 | 1,36% | 3 | 3,49% | 3 | 3,49% | 3 | 3,49% |
| Tostain (1980) | 3 | 1,36% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Boddaert & Daubenton (1783) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chappuis et al. (1974) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| dal Molin (2009) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Davant (1967) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson & Baker (2012) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Gill (1995) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Gmelin (1789) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gourreau et al. (1998) | 2 | 0,91% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Ingels et al. (2003) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Lepechin (1769) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martinet et al. (1765) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mathews (1914) | 2 | 0,91% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Mays et al. (2006) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Pezy et al. (2022) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Pons et al. (2005) | 2 | 0,91% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Sabine (1819) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Safford & Hawkins (2013) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Thibault et al. (2014) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Vieillot (1819) | 2 | 0,91% | 2 | 2,33% | 2 | 2,33% | 2 | 2,33% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Anonyme. (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré & Géraux (2004) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Beaufils (1999) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Bénito-espinal (1990) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Birdlife International (2016) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Boie (1835) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boschert & Dronneau (1998) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Brehm (1831) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Chastel et al. (1987) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Clements et al. (2015) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Clergeau & Pascal (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Clergeau et al. (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Clergeau et al. (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Contejean (2018) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Costrel & Corainville (1929) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Coues (1861) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crouzier (2009) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Deblock (1966) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Debout (2017) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Deflorenne et al. (2012) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Dollfus (1966) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois et al. (2008) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Efe et al. (2009) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Elkins & Yesou (1998) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gallien (2011) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Gernigon & Lacaze (2009) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Gernigon (2008) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guermeur (1987) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiguen et al. (1984) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Gunnerus (1767) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Homeyer (1853) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-mer (2011) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Isenmann et al. (1971) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| IUCN (2014) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Johnson (1973) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuhl (1820) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1831) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lethuillier (1999) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Lichtenstein (1823) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Vigne (2003) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louette & Cousin (1999) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Loury & Puissauve (2016) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Magaud & D'aubusson (1906) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Marion (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Montagu (1813) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Morrison (2006) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Naumann (1819) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nuttall (1834) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| O'reilly (1818) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| pallas (1764) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1769) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1776) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearson & Prévot (1971) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Phipps (1774) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prevot (1971) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Probst (1997) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Reeber et al. (1996) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reeber (2015) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Scopoli (1769) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siorat & Rocamora (1995) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Siorat et al. (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Siorat et al. (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Vanderwerf et al. (2004) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieillot (1817) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vincent (1990) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Yésou (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Yésou (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Yésou (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Yésou (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Yésou (2003) | 1 | 0,45% | 1 | 1,16% | 1 | 1,16% | 1 | 1,16% |
| Zilli (2021) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
