Acariens de Polynésie française
172 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ramage (2017) | 248 | 42,83% | 234 | 76,72% | 208 | 74,55% | 229 | 80,07% |
Hammer (1972) | 106 | 18,31% | 99 | 32,46% | 87 | 31,18% | 98 | 34,27% |
Sellnick (1959) | 63 | 10,88% | 41 | 13,44% | 37 | 13,26% | 37 | 12,94% |
Jacot (1934) | 48 | 8,29% | 20 | 6,56% | 12 | 4,3% | 17 | 5,94% |
Hammer (1972) | 46 | 7,94% | 29 | 9,51% | 29 | 10,39% | 29 | 10,14% |
Niedbała (1998) | 45 | 7,77% | 33 | 10,82% | 33 | 11,83% | 33 | 11,54% |
Subías (2009) | 38 | 6,56% | 38 | 12,46% | 35 | 12,54% | 38 | 13,29% |
Migeon (2015) | 37 | 6,39% | 37 | 12,13% | 37 | 13,26% | 37 | 12,94% |
Trägårdh (1952) | 33 | 5,7% | 12 | 3,93% | 12 | 4,3% | 12 | 4,2% |
Tenorio (1976) | 28 | 4,84% | 28 | 9,18% | 20 | 7,17% | 28 | 9,79% |
Vitzthum (1935) | 25 | 4,32% | 20 | 6,56% | 20 | 7,17% | 20 | 6,99% |
Jourdan (2020) | 24 | 4,15% | 23 | 7,54% | 20 | 7,17% | 22 | 7,69% |
Niedbała & Penttinen (2007) | 24 | 4,15% | 23 | 7,54% | 23 | 8,24% | 23 | 8,04% |
Hammes & Putoa (1986) | 23 | 3,97% | 23 | 7,54% | 23 | 8,24% | 23 | 8,04% |
Bartsch (1992) | 19 | 3,28% | 19 | 6,23% | 19 | 6,81% | 19 | 6,64% |
Jourdan & Mille (2006) | 18 | 3,11% | 17 | 5,57% | 17 | 6,09% | 17 | 5,94% |
Rageau (1959) | 16 | 2,76% | 15 | 4,92% | 11 | 3,94% | 15 | 5,24% |
Ermilov et al. (2013) | 15 | 2,59% | 15 | 4,92% | 15 | 5,38% | 14 | 4,9% |
Flechtmann et al. (1999) | 14 | 2,42% | 14 | 4,59% | 14 | 5,02% | 14 | 4,9% |
Vitzthum (1935) | 13 | 2,25% | 7 | 2,3% | 7 | 2,51% | 7 | 2,45% |
Ermilov & Mary (2020) | 11 | 1,9% | 11 | 3,61% | 9 | 3,23% | 9 | 3,15% |
Hammer (1971) | 11 | 1,9% | 9 | 2,95% | 9 | 3,23% | 9 | 3,15% |
Meurgey (2011) | 11 | 1,9% | 11 | 3,61% | 11 | 3,94% | 11 | 3,85% |
Adamson (1935) | 10 | 1,73% | 9 | 2,95% | 9 | 3,23% | 9 | 3,15% |
Gutierrez (1981) | 10 | 1,73% | 9 | 2,95% | 9 | 3,23% | 9 | 3,15% |
Mahunka (1982) | 10 | 1,73% | 10 | 3,28% | 10 | 3,58% | 9 | 3,15% |
Rageau (1958) | 10 | 1,73% | 7 | 2,3% | 7 | 2,51% | 7 | 2,45% |
Bartsch (2009) | 9 | 1,55% | 9 | 2,95% | 9 | 3,23% | 9 | 3,15% |
Ferris (1932) | 9 | 1,55% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Berlese (1918) | 8 | 1,38% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Flechtmann et al. (2000) | 8 | 1,38% | 8 | 2,62% | 8 | 2,87% | 8 | 2,8% |
Jacot (1934) | 7 | 1,21% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Niedbała & Liu (2023) | 7 | 1,21% | 6 | 1,97% | 6 | 2,15% | 6 | 2,1% |
Ermilov & Mary (2019) | 6 | 1,04% | 6 | 1,97% | 6 | 2,15% | 5 | 1,75% |
Niemi & Behan-Pelletier (2004) | 6 | 1,04% | 6 | 1,97% | 6 | 2,15% | 6 | 2,1% |
Bertrand & Ineich (1989) | 5 | 0,86% | 5 | 1,64% | 5 | 1,79% | 5 | 1,75% |
Brun et al. (1983) | 5 | 0,86% | 5 | 1,64% | 5 | 1,79% | 5 | 1,75% |
Etienne & Vilardebó (1978) | 5 | 0,86% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Gutierrez & Etienne (1986) | 5 | 0,86% | 5 | 1,64% | 5 | 1,79% | 5 | 1,75% |
Gutierrez (1968) | 5 | 0,86% | 5 | 1,64% | 5 | 1,79% | 5 | 1,75% |
Kreiter et al. (2020) | 5 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Mironov & Palma (2006) | 5 | 0,86% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Pritchard & Baker (1955) | 5 | 0,86% | 5 | 1,64% | 5 | 1,79% | 5 | 1,75% |
Aoki (1965) | 4 | 0,69% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Berlese (1921) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Beron (2021) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Flechtmann & Etienne (2006) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Hammer (1973) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Kreiter & Moraes (1997) | 4 | 0,69% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Lions (1966) | 4 | 0,69% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Mahunka (1985) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 3 | 1,05% |
Mahunka (1991) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Nava et al. (2018) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Niedbała (2000) | 4 | 0,69% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Otto (2000) | 4 | 0,69% | 4 | 1,31% | 4 | 1,43% | 4 | 1,4% |
Ramsay (1969) | 4 | 0,69% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Rivière (1979) | 4 | 0,69% | 3 | 0,98% | 3 | 1,08% | 2 | 0,7% |
Schicha (1979) | 4 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2001) | 4 | 0,69% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Atyeo & Gaud (1992) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Atyeo & Peterson (1992) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Beron (2020) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Beron (2021) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Bertrand & Ineich (1986) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Cochereau (1966) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Fan et al. (2016) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Flechtmann & Etienne (2005) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Guglielmone et al. (2023) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Haas et al. (2015) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 0 | 0% |
Hammer (1958) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 1 | 0,35% |
Liu & Zhang (2014) | 3 | 0,52% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Mahunka (1978) | 3 | 0,52% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Marciniak-Musial et al. (2022) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
McGregor (1950) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Niedbała (2017) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Rageau (1956) | 3 | 0,52% | 3 | 0,98% | 1 | 0,36% | 3 | 1,05% |
Schicha & Gutierrez (1985) | 3 | 0,52% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Schicha (1983) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Trave (1976) | 3 | 0,52% | 3 | 0,98% | 3 | 1,08% | 3 | 1,05% |
Adamson (1936) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2018) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Aoki (1959) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Aoki (1964) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Balogh (1960) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Bartsch (1992) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Berlese (1913) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Berlese (1913) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Castilho et al. (2016) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Dabert & Ehrnsberger (1999) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Dabert (2003) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Dadant & Etienne (1973) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Flechtmann & Etienne (2000) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Flechtmann & Etienne (2001) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Flechtmann et al. (1999) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Grandjean (1954) | 2 | 0,35% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Hammer (1979) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Klein et al. (1982) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Kreiter et al. (2002) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Kreiter et al. (2020) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Linnaeus (1758) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Ma et al. (2019) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Mahunka (1988) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahunka (1992) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Markel (1964) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
McGregor (1955) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Mironov et al. (2011) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Muñoz-Leal et al. (2017) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Oudemans (1912) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Peterson et al. (1980) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Quilici et al. (2000) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Robin & Megnin (1877) | 2 | 0,35% | 2 | 0,66% | 2 | 0,72% | 2 | 0,7% |
Schabetsberger et al. (2009) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 2 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Aoki (1994) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Auger et al. (2023) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Banks (1905) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Berlese (1905) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Berlese (1908) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Berlese (1910) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Berlese (1916) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Binetruy et al. (2019) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Canestrini (1897) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Chant & Mcmurtry (2004) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Cohic (1959) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Colloff (2009) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Cooreman (1959) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Datta (1985) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Dhondt (2005) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 0 | 0% |
D'souza & Jagannath (1982) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Ewing (1909) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fain & Pauly (2001) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Flechtmann & Etienne (2002) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Flechtmann & Etienne (2003) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Fourcroy (1785) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuller (1899) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Gaud et al. (1985) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Geijskes (1939) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean (1933) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hammer (1967) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hernandes et al. (2011) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Hirschmann (1985) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Hirst (1926) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Hüe et al. (2021) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Jacot (1923) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Keifer (1979) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Klompen & Johnson (2018) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Kreiter & Douin (2021) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Latreille (1806) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1807) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu et al. (2009) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahunka & Mahunka-Papp (1995) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Migeon et al. (2019) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Navajas et al. (2010) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Neumann (1901) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Niedbała & Starý (2015) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Niedbała (2007) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Oudemans (1915) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Prasad (1968) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Quilici et al. (1997) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Rageau & Vervent (1959) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Ramsay & Sheals (1969) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Roy et al. (2009) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Sayed (1946) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Schicha (1980) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Schicha (1984) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Schicha (1987) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Sengbusch (1957) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Starý & Block (1998) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Wallwork (1961) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |
Willmann (1931) | 1 | 0,17% | 1 | 0,33% | 0 | 0% | 1 | 0,35% |
Wood (1966) | 1 | 0,17% | 1 | 0,33% | 1 | 0,36% | 1 | 0,35% |