Amphipodes de Nouvelle-Calédonie
86 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Lowry (2007) | 190 | 52,92% | 178 | 77,06% | 178 | 77,06% | 178 | 77,06% |
| Ledoyer (1984) | 59 | 16,43% | 38 | 16,45% | 38 | 16,45% | 38 | 16,45% |
| Lowry & Stoddart (1994) | 44 | 12,26% | 44 | 19,05% | 44 | 19,05% | 44 | 19,05% |
| Peart & Hughes (2014) | 24 | 6,69% | 18 | 7,79% | 18 | 7,79% | 18 | 7,79% |
| Stock & Iliffe (1995) | 12 | 3,34% | 9 | 3,9% | 9 | 3,9% | 9 | 3,9% |
| Lowry & Fanini (2023) | 9 | 2,51% | 9 | 3,9% | 9 | 3,9% | 9 | 3,9% |
| Iannilli & Ruffo (2007) | 8 | 2,23% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
| Lowry & Myers (2003) | 8 | 2,23% | 8 | 3,46% | 8 | 3,46% | 8 | 3,46% |
| Peart (2004) | 8 | 2,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schellenberg (1938) | 8 | 2,23% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Ruffo & Paiotta (1972) | 7 | 1,95% | 3 | 1,3% | 3 | 1,3% | 3 | 1,3% |
| Chevreux (1915) | 6 | 1,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Myers (1986) | 6 | 1,67% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Bopiah & Hughes (2013) | 5 | 1,39% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
| Laval (1968) | 5 | 1,39% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
| Poupin et al. (1999) | 5 | 1,39% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
| Barnard (1972) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Barnard (1974) | 4 | 1,11% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Chevreux (1907) | 4 | 1,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hirayama (1990) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Lowry & Myers (2009) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Lowry & Myers (2019) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Lowry & Stoddart (1992) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Myers (1989) | 4 | 1,11% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Razouls & Thiriot (1968) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Stoddart & Lowry (2004) | 4 | 1,11% | 4 | 1,73% | 4 | 1,73% | 4 | 1,73% |
| Lowry & Stoddart (1995) | 3 | 0,84% | 3 | 1,3% | 3 | 1,3% | 3 | 1,3% |
| Richer de Forges et al. (2005) | 3 | 0,84% | 3 | 1,3% | 3 | 1,3% | 3 | 1,3% |
| Australian Museum (2020) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Barnard (1965) | 2 | 0,56% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Chevreux (1892) | 2 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevreux (1899) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Chevreux (1900) | 2 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corbari et al. (2020) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Fourt et al. (2017) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Guerra-garcia et al. (2023) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Hughes & Lowry (2015) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Iwasa-arai et al. (2017) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Jaume et al. (2007) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Jaume et al. (2009) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Laubitz (1995) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Ledoyer (1978) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Lowry & Hughes (2009) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Lowry (1981) | 2 | 0,56% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Mayer (1898) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Myers (1985) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Myers (2005) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Nagata (1961) | 2 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shoemaker (1934) | 2 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spandl (1926) | 2 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watson et al. (2004) | 2 | 0,56% | 2 | 0,87% | 2 | 0,87% | 2 | 0,87% |
| Audouin (1826) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Birstein (1960) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourcier (1988) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bovallius (1887) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Bulicheva (1955) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Clemente (2014) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Corbari (2015) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Corbari (2015) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Cousins et al. (2013) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Dana (1852) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Dana (1852) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1775) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forskål (1775) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Goud et al. (2021) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hirayama (1984) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Krapp-Schickel & Müller (2011) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Marchini et al. (2015) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Merlo et al. (2017) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Mills et al. (2018) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Müller (1990) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Müller (1992) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Myers (2012) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Oliveira (1954) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Perrier (1929) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Poisson & Legueux (1926) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin (1994) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Questel (2014) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Questel (2020) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Renon & Lefèvre (1985) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Rignault & Chevallier (2017) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Sheard (1938) | 1 | 0,28% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
| Spandl (1923) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1904) | 1 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
