Diplopodes
Diplopoda
185 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Kime & Enghoff (2017) | 117 | 10,1% | 98 | 20,99% | 98 | 21,83% | 95 | 20,83% |
Carl (1926) | 88 | 7,6% | 72 | 15,42% | 72 | 16,04% | 72 | 15,79% |
Brolemann (1935) | 64 | 5,53% | 52 | 11,13% | 49 | 10,91% | 49 | 10,75% |
Shelley & Lehtinen (1999) | 46 | 3,97% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Mauriès (1980) | 40 | 3,45% | 28 | 6% | 18 | 4,01% | 28 | 6,14% |
Mauriès (1969) | 39 | 3,37% | 20 | 4,28% | 20 | 4,45% | 20 | 4,39% |
Meurgey (2011) | 30 | 2,59% | 21 | 4,5% | 17 | 3,79% | 20 | 4,39% |
Ribaut (1913) | 26 | 2,25% | 20 | 4,28% | 20 | 4,45% | 20 | 4,39% |
Ramage et al. (2023) | 25 | 2,16% | 25 | 5,35% | 21 | 4,68% | 25 | 5,48% |
Mauriès (1961) | 24 | 2,07% | 18 | 3,85% | 17 | 3,79% | 17 | 3,73% |
Mauriès (1987) | 23 | 1,99% | 16 | 3,43% | 14 | 3,12% | 14 | 3,07% |
Iorio & Coulis (2020) | 17 | 1,47% | 15 | 3,21% | 12 | 2,67% | 15 | 3,29% |
Duborget (2017) | 16 | 1,38% | 16 | 3,43% | 16 | 3,56% | 15 | 3,29% |
Ribaut (1920) | 15 | 1,3% | 6 | 1,28% | 6 | 1,34% | 3 | 0,66% |
Geoffroy (2020) | 14 | 1,21% | 14 | 3% | 14 | 3,12% | 12 | 2,63% |
Vandenspiegel & Mathys (2021) | 14 | 1,21% | 14 | 3% | 14 | 3,12% | 14 | 3,07% |
Chamberlin (1918) | 13 | 1,12% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Schubart & Husson (1937) | 13 | 1,12% | 5 | 1,07% | 5 | 1,11% | 5 | 1,1% |
Mauriès (1990) | 12 | 1,04% | 11 | 2,36% | 6 | 1,34% | 11 | 2,41% |
Mauriès (2010) | 12 | 1,04% | 12 | 2,57% | 12 | 2,67% | 12 | 2,63% |
Silvestri (1897) | 12 | 1,04% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Coulis (2017) | 10 | 0,86% | 8 | 1,71% | 7 | 1,56% | 8 | 1,75% |
Ramage (2017) | 10 | 0,86% | 9 | 1,93% | 9 | 2% | 9 | 1,97% |
Risso (1827) | 10 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1900) | 9 | 0,78% | 9 | 1,93% | 9 | 2% | 9 | 1,97% |
Mauriès (1969) | 9 | 0,78% | 9 | 1,93% | 9 | 2% | 9 | 1,97% |
Brolemann (1894) | 8 | 0,69% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Brölemann (1921) | 8 | 0,69% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Noël et al. (2024) | 8 | 0,69% | 8 | 1,71% | 8 | 1,78% | 8 | 1,75% |
Porat (1888) | 8 | 0,69% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Mauriès & Nguyen Duy-Jacquemin (2001) | 7 | 0,6% | 5 | 1,07% | 5 | 1,11% | 5 | 1,1% |
Mauriès (1959) | 7 | 0,6% | 7 | 1,5% | 7 | 1,56% | 7 | 1,54% |
Verhoeff (1930) | 7 | 0,6% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Brölemann (1931) | 6 | 0,52% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Geoffroy & Mauries (1992) | 6 | 0,52% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Léger & Duboscq (1903) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaire et al. (2018) | 6 | 0,52% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Marek et al. (2003) | 6 | 0,52% | 5 | 1,07% | 5 | 1,11% | 5 | 1,1% |
Mauriès & Kime (1999) | 6 | 0,52% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Mauries (2019) | 6 | 0,52% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Nguyen Duy-Jacquemin (2002) | 6 | 0,52% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Ribaut (1908) | 6 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1947) | 6 | 0,52% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Ribaut (1952) | 6 | 0,52% | 6 | 1,28% | 6 | 1,34% | 6 | 1,32% |
Silvestri (1934) | 6 | 0,52% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Adamson (1932) | 5 | 0,43% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Brölemann (1926) | 5 | 0,43% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Fanzago (1877) | 5 | 0,43% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Mauriès (1976) | 5 | 0,43% | 5 | 1,07% | 5 | 1,11% | 5 | 1,1% |
Pocock (1898) | 5 | 0,43% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Ribaut (1955) | 5 | 0,43% | 2 | 0,43% | 2 | 0,45% | 0 | 0% |
Silvestri (1935) | 5 | 0,43% | 5 | 1,07% | 5 | 1,11% | 5 | 1,1% |
Brölemann (1900) | 4 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Ceuca (1962) | 4 | 0,35% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
De Almeida et al. (2021) | 4 | 0,35% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Golovatch & Sierwald (2001) | 4 | 0,35% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Jeekel (1963) | 4 | 0,35% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Mauriès (1983) | 4 | 0,35% | 4 | 0,86% | 4 | 0,89% | 4 | 0,88% |
Yokoyama (2013) | 4 | 0,35% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Bouzan et al. (2022) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Chamberlin (1920) | 3 | 0,26% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Geoffroy et al. (2022) | 3 | 0,26% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Golovatch et al. (2014) | 3 | 0,26% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Jourdan (2020) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Latzel (1892) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach ([1814]) | 3 | 0,26% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Leach ([1816]) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1963) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Mauriès (1967) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1974) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Mauriès (1983) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Mauries (1990) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Mesibov (2014) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Noël (2024) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Questel (2020) | 3 | 0,26% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Raphael (1970) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1907) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1951) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Sahli (1989) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Schubart (1958) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2014) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Stoev et al. (2010) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Strasser (1978) | 3 | 0,26% | 3 | 0,64% | 3 | 0,67% | 3 | 0,66% |
Adis et al. (1998) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Attems (1914) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1896) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brolemann (1897) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1897) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Condé & Jacquemin (1962) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Condé (1953) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Demange (1963) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Geoffroy & Mauriès (2017) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Gervais (1837) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffman (1977) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Hoffman (1981) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Jean-françois (2009) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Jeekel (1964) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Jeekel (1980) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeekel (2000) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Karsch (1881) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Latzel (1884) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Latzel (1884) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1895) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger & Duboscq (1903) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès (1960) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Mauriès (1981) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Nguyen Duy-Jacquemin (2014) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Questel & Le Quellec (2012) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1909) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Ribaut (1951) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Ribaut (1954) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Sahli (1974) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Schubart (1958) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Schubart (1962) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Shelley (2002) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Silvestri (1903) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Silvestri (1904) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Théodoridès & Ormières (1959) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandenspiegel et al. (2021) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Verhoeff (1894) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1936) | 2 | 0,17% | 2 | 0,43% | 2 | 0,45% | 2 | 0,44% |
Verhoeff (1943) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Aberlenc (2016) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1984) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Antić & Spelda (2022) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Attems (1900) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Attems (1953) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigler (1913) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Borreguero & Preisig (2023) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Brade-Birks (1920) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brolemann (1897) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brolemann (1905) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brölemann (1932) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Brölemann (1905) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Chamberlin (1920) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Condé & Demange (1961) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Conde (1950) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Djursvoll (2019) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Faës (1902) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1990) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Geoffroy (2016) | 1 | 0,09% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
Geoffroy (2020) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Geoffroy (2021) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Gilgado et al. (2022) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Golovatch et al. (2007) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Hoess & Scholl (2001) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Kime & Enghoff (2011) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Kime & Enghoff (2021) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Latzel (1884) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Latzel (1895) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Likhitrakarn et al. (2014) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Loomis (1934) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1872) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mauriès & Vicente (1977) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Mauriès (1988) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Mauriès (2015) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Mendes (1986) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesibov (2009) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Nguyen & Duy-jacquemin (2000) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Noël & Geoffroy (2020) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Peters (1864) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1930) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Pocock (1893) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Rabaud (1918) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1904) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1905) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribaut (1909) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Rothenbühler (1899) | 1 | 0,09% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
Sahli & Pages (1978) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Seurat (1934) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Shelley & Martinez-Torres (2013) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Sierwald (2009) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Silvestri (1894) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Silvestri (1904) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Spelda (2014) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Srisonchai et al. (2018) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Ting et al. (2022) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Van et al. (1984) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Vandenspiegel & Golovatch (2007) | 1 | 0,09% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
Verhoeff (1896) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1902) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1932) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer & Gervais (1847) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |