Oiseaux de Saint-Barthélemy
Aves de Saint-Barthélemy
198 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) | 142 | 34,22% | 136 | 69,39% | 114 | 72,61% | 126 | 79,75% |
Questel (2020) | 142 | 34,22% | 137 | 69,9% | 111 | 70,7% | 133 | 84,18% |
UICN Comité français, OFB & MNHN (2021) | 130 | 31,33% | 130 | 66,33% | 130 | 82,8% | 94 | 59,49% |
Yokoyama (2013) | 117 | 28,19% | 103 | 52,55% | 95 | 60,51% | 77 | 48,73% |
Questel & Le Quellec (2012) | 113 | 27,23% | 108 | 55,1% | 88 | 56,05% | 94 | 59,49% |
Uicn et al. (2017) | 108 | 26,02% | 104 | 53,06% | 97 | 61,78% | 78 | 49,37% |
Remsen et al. (2013) | 75 | 18,07% | 72 | 36,73% | 72 | 45,86% | 51 | 32,28% |
Belfan & Conde (2016) | 54 | 13,01% | 52 | 26,53% | 37 | 23,57% | 50 | 31,65% |
Linnaeus (1758) | 54 | 13,01% | 16 | 8,16% | 16 | 10,19% | 8 | 5,06% |
Etcheberry & Abraham (2009) | 39 | 9,4% | 34 | 17,35% | 34 | 21,66% | 28 | 17,72% |
Uicn et al. (2015) | 31 | 7,47% | 30 | 15,31% | 30 | 19,11% | 16 | 10,13% |
Dewynter (2021) | 25 | 6,02% | 25 | 12,76% | 25 | 15,92% | 24 | 15,19% |
Weimerskirch et al. (2009) | 25 | 6,02% | 19 | 9,69% | 19 | 12,1% | 9 | 5,7% |
Uicn et al. (2020) | 24 | 5,78% | 24 | 12,24% | 24 | 15,29% | 20 | 12,66% |
Tostain et al. (2013) | 19 | 4,58% | 15 | 7,65% | 14 | 8,92% | 12 | 7,59% |
Clements (2012) | 18 | 4,34% | 18 | 9,18% | 17 | 10,83% | 14 | 8,86% |
Gmelin (1789) | 17 | 4,1% | 3 | 1,53% | 3 | 1,91% | 3 | 1,9% |
Linnaeus (1766) | 14 | 3,37% | 2 | 1,02% | 1 | 0,64% | 1 | 0,63% |
Barau et al. (2005) | 13 | 3,13% | 11 | 5,61% | 11 | 7,01% | 8 | 5,06% |
Uicn et al. (2015) | 13 | 3,13% | 12 | 6,12% | 12 | 7,64% | 11 | 6,96% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 12 | 2,89% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Clements et al. (2015) | 11 | 2,65% | 11 | 5,61% | 1 | 0,64% | 10 | 6,33% |
Dickinson & Remsen (2013) | 10 | 2,41% | 9 | 4,59% | 6 | 3,82% | 8 | 5,06% |
Bénito-espinal (1990) | 8 | 1,93% | 7 | 3,57% | 2 | 1,27% | 7 | 4,43% |
Commission de l’Avifaune Française (2016) | 8 | 1,93% | 8 | 4,08% | 8 | 5,1% | 4 | 2,53% |
Guth (1971) | 8 | 1,93% | 7 | 3,57% | 7 | 4,46% | 4 | 2,53% |
Rocamora (2004) | 8 | 1,93% | 8 | 4,08% | 7 | 4,46% | 5 | 3,16% |
Gill (1995) | 7 | 1,69% | 7 | 3,57% | 7 | 4,46% | 2 | 1,27% |
Thibault et al. (2014) | 7 | 1,69% | 7 | 3,57% | 7 | 4,46% | 2 | 1,27% |
Del Hoyo & Collar (2014) | 6 | 1,45% | 3 | 1,53% | 3 | 1,91% | 3 | 1,9% |
Gmelin (1788) | 6 | 1,45% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Vieillot (1819) | 6 | 1,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock et al. (1960) | 5 | 1,2% | 3 | 1,53% | 3 | 1,91% | 2 | 1,27% |
Lee & Walsh-McGehee (2000) | 5 | 1,2% | 5 | 2,55% | 0 | 0% | 5 | 3,16% |
Safford & Hawkins (2013) | 5 | 1,2% | 5 | 2,55% | 5 | 3,18% | 3 | 1,9% |
Birdlife International (2016) | 4 | 0,96% | 4 | 2,04% | 4 | 2,55% | 0 | 0% |
Collier et al. (2002) | 4 | 0,96% | 4 | 2,04% | 3 | 1,91% | 2 | 1,27% |
Dewynter & Claessens (2020) | 4 | 0,96% | 4 | 2,04% | 4 | 2,55% | 1 | 0,63% |
Ehrhardt (1971) | 4 | 0,96% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Furminieux (2019) | 4 | 0,96% | 4 | 2,04% | 4 | 2,55% | 4 | 2,53% |
Levesque & Delcroix (2016) | 4 | 0,96% | 3 | 1,53% | 1 | 0,64% | 3 | 1,9% |
Dubois et al. (2008) | 3 | 0,72% | 3 | 1,53% | 3 | 1,91% | 3 | 1,9% |
Gargominy et al. (1996) | 3 | 0,72% | 3 | 1,53% | 3 | 1,91% | 3 | 1,9% |
Gonzalez et al. (2009) | 3 | 0,72% | 0 | 0% | 0 | 0% | 0 | 0% |
Humphries et al. (2019) | 3 | 0,72% | 3 | 1,53% | 3 | 1,91% | 0 | 0% |
Karadjian et al. (2022) | 3 | 0,72% | 3 | 1,53% | 3 | 1,91% | 3 | 1,9% |
Levesque & Delcroix (2013) | 3 | 0,72% | 3 | 1,53% | 0 | 0% | 3 | 1,9% |
Oustalet (1895) | 3 | 0,72% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Tostain (1980) | 3 | 0,72% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Ausilio & Zotier (1989) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 1 | 0,63% |
Boddaert & Daubenton (1783) | 2 | 0,48% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Chartier et al. (2007) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
dal Molin (2009) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Daniel et al. (2020) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Davant (1967) | 2 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1816) | 2 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Impact-mer (2011) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Ingels et al. (2003) | 2 | 0,48% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Kojadinovic et al. (2007) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Levesque & Clergeau (2002) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Lorvelec et al. (2004) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Louette & Cousin (1999) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Mathews (1914) | 2 | 0,48% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
McNair & Cramer-Burke (2006) | 2 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Potin (2013) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Powell et al. (2008) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Theuerkauf et al. (2010) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Tunstall (1880) | 2 | 0,48% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Vanderwerf et al. (2006) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 1 | 0,63% |
Weimerskirch et al. (2009) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 0 | 0% |
Wilson (1813) | 2 | 0,48% | 2 | 1,02% | 2 | 1,27% | 2 | 1,27% |
Anonyme (2008) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Anonyme. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Bangs (1913) | 1 | 0,24% | 1 | 0,51% | 0 | 0% | 1 | 0,63% |
Barre et al. (1991) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Bertault (1988) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1982) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Birdlife International (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Birdlife International (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Birdlife International (2017) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Boschert & Dronneau (1998) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Brandt (1838) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun (1958) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Calenge et al. (2010) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Chastel et al. (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Cheke & Hume (2008) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
CHN (2017) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Clements (1992) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Clergeau & Pascal (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Coatmeur (1999) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Coues (1862) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Crochet et al. (2022) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Crouzier (2009) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Csabaï (2020) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Danforth (1935) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Daszkiewicz, P. & Massary, J.-C. de 2006. Overlooked historical testimony as to the presence of Red-billed Tropicbird Phaeton aethereus in French Guiana. Bulletin of the British Ornithologists'Club, 126(1): 71-73.">Daszkiewicz & Massary (2006) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Daudin (1802) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Deblock (1966) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Debout (2001) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Debout (2009) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Dechelle & Ingels (2007) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Deflandre (2007) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Delacour (1963) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Deniau & Provost (2020) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Dreff & Delliere (1994) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Ducatez & Devore (2023) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Efe et al. (2009) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Eyton (1838) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Fremont (2002) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Gallien (2011) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Gernigon (2008) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Guermeur (1987) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Huey (1927) | 1 | 0,24% | 1 | 0,51% | 0 | 0% | 1 | 0,63% |
Kuhl (1820) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Leblond (2003) | 1 | 0,24% | 1 | 0,51% | 0 | 0% | 1 | 0,63% |
Lesson (1831) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Lesson (1839) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Levesque (2001) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Levesque (2013) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Linné (1766) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Loison (1989) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Lorvelec et al. (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Lorvelec et al. (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Marion & Clergeau (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Marion (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Marion (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Melin et al. (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Montagu (1813) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Morrison (2006) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Nadal & Tariel (2008) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
O'reilly (1818) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Pearman et al. (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Peters (1930) | 1 | 0,24% | 1 | 0,51% | 0 | 0% | 1 | 0,63% |
Probst (1997) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Purenne (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Reeber (2015) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Robert et al. (2002) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Routtier et al. (2023) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Roux & Coll. (2017) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez et al. (2004) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Schuchmann (1981) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Scopoli (1786) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Socolovschi et al. (2012) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Spiroux (1996) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Steadman & Bollt (2010) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Swainson (1838) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Tostain & Dujardin (1988) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Uicn et al. (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
UNEP-WCMC (2005) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Vanderwerf et al. (2004) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Verreaux & Des Murs (1860) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Vieillot (1816) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Wahl & Barbraud (2005) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 0 | 0% |
Yésou (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |
Yésou (2003) | 1 | 0,24% | 1 | 0,51% | 1 | 0,64% | 1 | 0,63% |