Mammifères marins de la Réunion
118 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Rinaldi (2016) | 100 | 21,79% | 100 | 333,33% | 100 | 400% | 80 | 320% |
Carzon et al. (2016) | 75 | 16,34% | 75 | 250% | 75 | 300% | 60 | 240% |
Estrade et al. (2016) | 75 | 16,34% | 75 | 250% | 75 | 300% | 60 | 240% |
Uicn et al. (2015) | 36 | 7,84% | 36 | 120% | 36 | 144% | 28 | 112% |
Charrassin (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Charrassin (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Jarrett & Shirihai (2014) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Moutou (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Spitz et al. (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Thoisy & Bordin (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
Urtizberea (2016) | 25 | 5,45% | 25 | 83,33% | 25 | 100% | 20 | 80% |
G.E.M.M. (2012) | 21 | 4,58% | 21 | 70% | 21 | 84% | 16 | 64% |
Garrigue (2007) | 20 | 4,36% | 20 | 66,67% | 20 | 80% | 16 | 64% |
Bordin et al. (2021) | 19 | 4,14% | 19 | 63,33% | 19 | 76% | 14 | 56% |
Gannier (2001) | 18 | 3,92% | 18 | 60% | 18 | 72% | 14 | 56% |
Gannier (2002) | 17 | 3,7% | 17 | 56,67% | 17 | 68% | 13 | 52% |
Kiszka et al.(2007) | 17 | 3,7% | 16 | 53,33% | 16 | 64% | 12 | 48% |
Catzeflis (2012) | 16 | 3,49% | 16 | 53,33% | 16 | 64% | 11 | 44% |
Dewynter et al. (2021) | 16 | 3,49% | 16 | 53,33% | 16 | 64% | 13 | 52% |
Gannier (2009) | 16 | 3,49% | 16 | 53,33% | 16 | 64% | 12 | 48% |
Aulagnier (2009) | 15 | 3,27% | 14 | 46,67% | 14 | 56% | 11 | 44% |
Gannier (2000) | 15 | 3,27% | 15 | 50% | 15 | 60% | 11 | 44% |
Kiszka et al. (2010) | 15 | 3,27% | 15 | 50% | 15 | 60% | 12 | 48% |
Dulau-Drouot et al. (2008) | 13 | 2,83% | 13 | 43,33% | 13 | 52% | 9 | 36% |
Laran et al. (2011) | 13 | 2,83% | 13 | 43,33% | 13 | 52% | 10 | 40% |
Uicn et al. (2017) | 13 | 2,83% | 13 | 43,33% | 13 | 52% | 8 | 32% |
Perrin et al. (2002) | 9 | 1,96% | 9 | 30% | 9 | 36% | 7 | 28% |
Samaran & Guinet (2009) | 9 | 1,96% | 9 | 30% | 9 | 36% | 7 | 28% |
Linnaeus (1758) | 8 | 1,74% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Questel (2020) | 8 | 1,74% | 8 | 26,67% | 8 | 32% | 4 | 16% |
Shirihai (2003) | 8 | 1,74% | 8 | 26,67% | 8 | 32% | 6 | 24% |
Questel & Le Quellec (2012) | 7 | 1,53% | 7 | 23,33% | 7 | 28% | 3 | 12% |
Robineau & Duhamel (2006) | 6 | 1,31% | 6 | 20% | 6 | 24% | 4 | 16% |
Boer et al. (1999) | 5 | 1,09% | 5 | 16,67% | 5 | 20% | 5 | 20% |
IUCN (2012) | 5 | 1,09% | 5 | 16,67% | 5 | 20% | 3 | 12% |
Rossi-santos et al. (2007) | 5 | 1,09% | 5 | 16,67% | 5 | 20% | 3 | 12% |
Desbrosses & Etcheberry (1987) | 4 | 0,87% | 3 | 10% | 3 | 12% | 1 | 4% |
AAMP (2012) | 3 | 0,65% | 3 | 10% | 3 | 12% | 0 | 0% |
Ainley et al. (2007) | 3 | 0,65% | 3 | 10% | 3 | 12% | 2 | 8% |
Boer (2000) | 3 | 0,65% | 3 | 10% | 3 | 12% | 2 | 8% |
Cottarel et al. (2013) | 3 | 0,65% | 3 | 10% | 3 | 12% | 3 | 12% |
Laran et al. (2012) | 3 | 0,65% | 3 | 10% | 3 | 12% | 2 | 8% |
Matsuoka et al. (2005) | 3 | 0,65% | 3 | 10% | 3 | 12% | 1 | 4% |
Prévost & Mougin (1970) | 3 | 0,65% | 3 | 10% | 3 | 12% | 2 | 8% |
Robineau (2005) | 3 | 0,65% | 3 | 10% | 3 | 12% | 1 | 4% |
Uicn et al. (2020) | 3 | 0,65% | 3 | 10% | 3 | 12% | 2 | 8% |
Boer & Simmonds (2000) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Diaz & Cuzange (2009) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Gannier & Petiau (2006) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 0 | 0% |
Kasamatsu & Joyce (1995) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Kock et al. (2006) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Leaper et al. (2008) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 1 | 4% |
Leaper et al. (2008) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Robineau (1989) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Thiele et al. (1999) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Thiele et al. (2004) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 1 | 4% |
Van Canneytet al. (2008) | 2 | 0,44% | 2 | 6,67% | 2 | 8% | 2 | 8% |
Abril et al. (1986) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Andrew et al. (2008) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Anonyme. (2004) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Berta & Churchill (2012) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Best & Scott (1993) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Best et al. (1995) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Borsa (1997) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Branch (2010) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Carzon (2012) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Cerchio et al. (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Clapham et al. (1999) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Collectif (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Cotte et al. (2001) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Dalebout et al. (2005) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Ersts & Rosenbaum (2003) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Fleming & Jackson (2011) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Garrigue & Poupon (2013) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Gill & Thiele (1997) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Gillespie (1997) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Goodall et al. (1997) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Gray (1846) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1864) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1865) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1872) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Guinet (2004) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Hedley et al. (2007) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Heimlich-boran (1993) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Jefferson & Barros (1997) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Jehl et al. (1980) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Johnson & Wolman (1984) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Kasamatsu et al. (2000) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Kawamura (1994) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Labach et al. (2021) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Leatherwood et al. (1979) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Macleod et al. (2006) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Murase et al. (2002) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Nicol et al. (2000) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Okamura & Kitakado (2008) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Oremus (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Perrin et al. (1994) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Pitman & Ensor (2003) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Praderi et al. (1992) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Riccialdelli et al. (2010) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Richards (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Roche & Guinet (2007) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Rosenbaum & Collins (2006) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Samaran (2008) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Sirovic et al. (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Smith et al. (2005) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
UICN (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Viale & Frontier (1989) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Weerdt (2023) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Williams et al. (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 0 | 0% |
Wursig & Wursig (1980) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |
Zelhuber (2009) | 1 | 0,22% | 1 | 3,33% | 1 | 4% | 1 | 4% |