Poissons d'eau douce de la Réunion
102 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Keith et al. (2006) | 58 | 8,59% | 43 | 67,19% | 41 | 66,13% | 42 | 67,74% |
Fricke et al. (2009) | 45 | 6,67% | 35 | 54,69% | 34 | 54,84% | 34 | 54,84% |
Fricke et al. (2011) | 23 | 3,41% | 19 | 29,69% | 19 | 30,65% | 19 | 30,65% |
Keith et al. (2013) | 22 | 3,26% | 16 | 25% | 16 | 25,81% | 16 | 25,81% |
Wickel & Jamon (2010) | 22 | 3,26% | 17 | 26,56% | 16 | 25,81% | 17 | 27,42% |
Soubeyran (2008) | 19 | 2,81% | 17 | 26,56% | 17 | 27,42% | 17 | 27,42% |
Siu et al. (2017) | 17 | 2,52% | 11 | 17,19% | 11 | 17,74% | 11 | 17,74% |
Keith et al. (2002) | 12 | 1,78% | 8 | 12,5% | 8 | 12,9% | 8 | 12,9% |
Séret (1997) | 10 | 1,48% | 10 | 15,62% | 10 | 16,13% | 10 | 16,13% |
Causse et al. (2023) | 8 | 1,19% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Gargominy et al. (1996) | 6 | 0,89% | 6 | 9,38% | 6 | 9,68% | 6 | 9,68% |
Keith et al. (2011) | 6 | 0,89% | 6 | 9,38% | 6 | 9,68% | 6 | 9,68% |
Keith et al. (2014) | 6 | 0,89% | 6 | 9,38% | 6 | 9,68% | 6 | 9,68% |
Kulbicki (comm. pers., 2011) | 6 | 0,89% | 5 | 7,81% | 5 | 8,06% | 5 | 8,06% |
Keith et al. (1999) | 5 | 0,74% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Keith et al. (2009) | 5 | 0,74% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Keith (2002) | 5 | 0,74% | 5 | 7,81% | 5 | 8,06% | 5 | 8,06% |
Pascal et al. (2006) | 5 | 0,74% | 5 | 7,81% | 5 | 8,06% | 5 | 8,06% |
Delrieu-Trottin et al. (2015) | 4 | 0,59% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Jordan (1894) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2011) | 4 | 0,59% | 4 | 6,25% | 4 | 6,45% | 4 | 6,45% |
Latham (1794) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 4 | 0,59% | 4 | 6,25% | 4 | 6,45% | 4 | 6,45% |
Monti et al. (2010) | 4 | 0,59% | 4 | 6,25% | 4 | 6,45% | 4 | 6,45% |
Bacchet et al. (2007) | 3 | 0,44% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Brosse et al. (2021) | 3 | 0,44% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Duméril (1865) | 3 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2013) | 3 | 0,44% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Jourdan (2020) | 3 | 0,44% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Kottelat ( 2013) | 3 | 0,44% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Marquet et al. (2003) | 3 | 0,44% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Mennesson & Keith (2017) | 3 | 0,44% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Williams et al. (2006) | 3 | 0,44% | 3 | 4,69% | 3 | 4,84% | 3 | 4,84% |
Alley et al. (2023) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Béarez et al. (2017) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Bloch & Schneider (1801) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Faria et al. (2013) | 2 | 0,3% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Fernandez-Carvalho et al. (2013) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Feutry et al. (2012) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Fischer (1884) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1896) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2006) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Legand (1950) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Lim et al. (2002) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Mennesson et al. (2019) | 2 | 0,3% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Pallas [1814] | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Persat & Keith (1997) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Questel & Le Quellec (2012) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Questel (2020) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Teichert et al. (2013) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
UICN France & MNHN (2013) | 2 | 0,3% | 2 | 3,12% | 2 | 3,23% | 2 | 3,23% |
Audige (1927) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Béarez & Séret (2009) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Bloch & Schneider (1801) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1912) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Chabanet & Durville (2005) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Couteyen (2006) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Denys et al. (2014) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Duhamel et al. (2005) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Firmat & Alibert (2011) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourriére et al. (2014) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Gentry et al. (2004) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Girard (1859) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Girard (1859) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gozlan et al. (2010) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Haÿ et al. (2023) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Jordan (1892) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1895) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Dorson (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith & Dorson (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith & Dorson (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith & Dorson (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith & Mennesson (2021) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Keith (2003) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Kronen et al. (2009) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Kulbicki et al. (2000) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Le Bail et al. (2012) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Letourneur et al. (2004) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Loiselle & Stiassny (2007) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Lorvelec & Pascal (2009) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Maeda et al. (2011) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsuzaki et al. (2009) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Mennesson & Keith (2020) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Nelson-Smith et al. (2014) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Ocea & Consult' (2015) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1770) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Peters (1852) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve & Poulet (2015) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Rafinesque (1820) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1997) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |
Walbaum (1792) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,15% | 1 | 1,56% | 1 | 1,61% | 1 | 1,61% |