Arachnides de la Réunion
267 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Cazanove (2022) | 130 | 15,03% | 127 | 41,23% | 127 | 41,5% | 127 | 41,5% |
Kreiter et al. (2020) | 81 | 9,36% | 41 | 13,31% | 41 | 13,4% | 41 | 13,4% |
Mahunka (1978) | 55 | 6,36% | 26 | 8,44% | 26 | 8,5% | 26 | 8,5% |
Kreiter et al. (2002) | 44 | 5,09% | 33 | 10,71% | 33 | 10,78% | 33 | 10,78% |
Ramage (2017) | 43 | 4,97% | 40 | 12,99% | 40 | 13,07% | 40 | 13,07% |
Migeon (2015) | 32 | 3,7% | 32 | 10,39% | 32 | 10,46% | 32 | 10,46% |
Nentwig et al. (2019) | 32 | 3,7% | 31 | 10,06% | 31 | 10,13% | 31 | 10,13% |
Mahunka (1988) | 27 | 3,12% | 8 | 2,6% | 8 | 2,61% | 8 | 2,61% |
Quilici et al. (2000) | 24 | 2,77% | 20 | 6,49% | 20 | 6,54% | 20 | 6,54% |
Berland (1933) | 22 | 2,54% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Jourdan & Mille (2006) | 22 | 2,54% | 19 | 6,17% | 19 | 6,21% | 19 | 6,21% |
Vayssières et al. (2001) | 22 | 2,54% | 17 | 5,52% | 17 | 5,56% | 17 | 5,56% |
Ledoux (2007) | 21 | 2,43% | 19 | 6,17% | 19 | 6,21% | 19 | 6,21% |
Meurgey (2011) | 20 | 2,31% | 16 | 5,19% | 16 | 5,23% | 16 | 5,23% |
Dierkens & Charlat (2011) | 18 | 2,08% | 15 | 4,87% | 15 | 4,9% | 15 | 4,9% |
Ledoux (2004) | 18 | 2,08% | 13 | 4,22% | 13 | 4,25% | 13 | 4,25% |
Berland (1934) | 15 | 1,73% | 9 | 2,92% | 9 | 2,94% | 9 | 2,94% |
Berland (1934) | 15 | 1,73% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Dierkens & Ramage (2016) | 15 | 1,73% | 14 | 4,55% | 14 | 4,58% | 14 | 4,58% |
Gutierrez & Etienne (1986) | 15 | 1,73% | 14 | 4,55% | 14 | 4,58% | 14 | 4,58% |
Berland (1942) | 14 | 1,62% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Ledoux & Hallé (1995) | 14 | 1,62% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Berland (1924) | 13 | 1,5% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Niedbała (2017) | 13 | 1,5% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Platnick (1993) | 13 | 1,5% | 8 | 2,6% | 8 | 2,61% | 8 | 2,61% |
Quilici et al. (1997) | 13 | 1,5% | 13 | 4,22% | 13 | 4,25% | 13 | 4,25% |
Mahnert (1975) | 12 | 1,39% | 12 | 3,9% | 9 | 2,94% | 12 | 3,92% |
Souza et al. (2019) | 12 | 1,39% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Vedel et al. (2013) | 12 | 1,39% | 12 | 3,9% | 12 | 3,92% | 12 | 3,92% |
Hammes & Putoa (1986) | 11 | 1,27% | 11 | 3,57% | 11 | 3,59% | 11 | 3,59% |
Jourdan (2020) | 11 | 1,27% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Kreiter et al. (2013) | 11 | 1,27% | 11 | 3,57% | 11 | 3,59% | 11 | 3,59% |
Berland (1935) | 10 | 1,16% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Dierkens (2021) | 10 | 1,16% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Flechtmann et al. (2000) | 10 | 1,16% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Guglielmone et al. (2023) | 10 | 1,16% | 10 | 3,25% | 10 | 3,27% | 10 | 3,27% |
Kreiter et al. (2018) | 9 | 1,04% | 9 | 2,92% | 9 | 2,94% | 9 | 2,94% |
Kreiter et al. (2020) | 9 | 1,04% | 9 | 2,92% | 9 | 2,94% | 9 | 2,94% |
Gutierrez (1968) | 8 | 0,92% | 8 | 2,6% | 8 | 2,61% | 8 | 2,61% |
Lopez (1990) | 8 | 0,92% | 8 | 2,6% | 8 | 2,61% | 8 | 2,61% |
Questel (2020) | 8 | 0,92% | 8 | 2,6% | 8 | 2,61% | 8 | 2,61% |
Bonaldo & Brescovit (1992) | 7 | 0,81% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Delfosse (2024) | 7 | 0,81% | 7 | 2,27% | 6 | 1,96% | 7 | 2,29% |
Flechtmann et al. (1999) | 7 | 0,81% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Hervé & Garrouste (2009) | 7 | 0,81% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Jacquot et al. (2016) | 7 | 0,81% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Pritchard & Baker (1962) | 7 | 0,81% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Roger (2018) | 7 | 0,81% | 7 | 2,27% | 7 | 2,29% | 7 | 2,29% |
Taczanowski (1874) | 7 | 0,81% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Aharon et al. (2017) | 6 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1929) | 6 | 0,69% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Hullé et al. (2018) | 6 | 0,69% | 6 | 1,95% | 6 | 1,96% | 6 | 1,96% |
Schmidt & Jocqué (1983) | 6 | 0,69% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Yokoyama (2013) | 6 | 0,69% | 6 | 1,95% | 6 | 1,96% | 6 | 1,96% |
Delfosse (2017) | 5 | 0,58% | 5 | 1,62% | 5 | 1,63% | 4 | 1,31% |
Dupérré (2023) | 5 | 0,58% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Etienne & Vilardebó (1978) | 5 | 0,58% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Gutierrez (1981) | 5 | 0,58% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Hammer (1972) | 5 | 0,58% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Harvey (2011) | 5 | 0,58% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Huber et al. (2023) | 5 | 0,58% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
Kury et al. (2024) | 5 | 0,58% | 5 | 1,62% | 4 | 1,31% | 5 | 1,63% |
Nibouche et al. (202X) | 5 | 0,58% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Niedbała & Liu (2023) | 5 | 0,58% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Questel & Le Quellec (2012) | 5 | 0,58% | 5 | 1,62% | 5 | 1,63% | 5 | 1,63% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 5 | 0,58% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Bigot (1992) | 4 | 0,46% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Etienne & Flechtmann (2006) | 4 | 0,46% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Kreiter & Moraes (1997) | 4 | 0,46% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Mahunka (1978) | 4 | 0,46% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Mahunka (1985) | 4 | 0,46% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Marples (1957) | 4 | 0,46% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Niedbała & Penttinen (2007) | 4 | 0,46% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Niedbała & Starý (2015) | 4 | 0,46% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Rémy (1950) | 4 | 0,46% | 4 | 1,3% | 4 | 1,31% | 4 | 1,31% |
Vinson (1863) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1802) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1935) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Baker & Pritchard (1960) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Beatty et al. (2008) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Berland (1927) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Berry et al. (1998) | 3 | 0,35% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Bonnet (1924) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Brun et al. (1983) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Cazanove et al. (2022) | 3 | 0,35% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Cochereau (1966) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Duhamel (2018) | 3 | 0,35% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Gasnier et al. (2015) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Gutierrez (1982) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Hullé & Vernon (2021) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Maquart et al. (2018) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Parola & Barré (2004) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Rageau (1958) | 3 | 0,35% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Simon (1897) | 3 | 0,35% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Smit et al. (2023) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
Taczanowski (1871) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal & Vansteene (2021) | 3 | 0,35% | 3 | 0,97% | 3 | 0,98% | 3 | 0,98% |
(2022) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Adamson (1936) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Anderson & Trueman (2000) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2018) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Baehr et al. (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Balogh (1961) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Barre et al. (1988) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Barré et al. (2001) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1986) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Beron (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Berry et al. (1997) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Blommers (1974) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Brignoli (1981) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Bryant (1942) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Caporiacco & Denis (1954) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Channabasavanna (1966) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Chevalier & Dewynter (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Courtial (2023) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dadant & Etienne (1973) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Doleschall (1857) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Enders (1993) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann & Etienne (2000) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann & Etienne (2001) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann & Etienne (2005) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann & Etienne (2006) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann & Moraes (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Flechtmann et al. (1999) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Gaud & Atyeo (1986) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Gaud & Atyeo (1987) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Grandjean (1933) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Hacala et al. (2024) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Hammer (1961) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Hammer (1979) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Kemal (2008) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Klein et al. (1982) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Kreiter & Douin (2021) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Lawrence (1969) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourenço (1987) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Migeon et al. (2019) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Moraes et al. (2006) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Muma (1955) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz-Leal et al. (2017) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Narita et al. (2013) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Niedbała (1994) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Niedbała (1998) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Odin (2014) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Odin (2017) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Oudemans (1912) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pritchard & Baker (1955) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Rageau (1956) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Raven (2015) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Remy (1952) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Roberts (2014) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Schicha & Gutierrez (1985) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Smith et al. (1989) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1872) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2020) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Ueckermann & Loots (1985) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitzthum (1935) | 2 | 0,23% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Walckenaer ([1841]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Walzer et al. (2007) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
Yaginuma (1972) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaher & Shehata (1966) | 2 | 0,23% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
André (1932) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Audouin (1826) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Auger et al. (2023) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Balogh (1958) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Banks (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Banks (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré & Camus (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (1991) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Binetruy et al. (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Blommers (1976) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosmans & Hervé (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambridge (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cazanove (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Chinniah & Mohanasundaram (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Cicculli et al. (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Cohic (1959) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Conte et al. (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Coulis (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Couteyen (2021) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dandeu et al. (1991) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Déjean et al. (2023) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Déjean (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dierkens (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dierkens (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dönitz (1910) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Dosse (1958) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufour (1831) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Eldin et al. (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Emerit & Ledoux (2008) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Esnault et al. (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Fabricius (1798) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Etienne (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Forskål (1775) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Fourcroy (1785) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gaud & Atyeo (1976) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gaud (1953) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Geijskes (1939) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gillespie (2003) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Gonzalez-rodriguez (1963) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Grandjean (1936) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gupta (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Jäger (2002) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1836) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kreiter et al. (2000) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Kreiter et al. (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Kuntner et al. (2018) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lamontellerie (1965) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Le Conte et al. (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lecigne et al. (2021) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Leon (1965) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Lourenço (1983) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Luo (2023) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Mahunka (1973) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Mahunka (1982) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Mahunka (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mammola & Milano (2019) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Maréchal & Iinuma (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Marie & Vetter (2015) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Mello-leitao (1942) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mello-Leitão (1945) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Moraes et al. (2000) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Morais et al. (2016) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Nardi et al. (2023) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Navajas et al. (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Nentwig & Kobelt (2010) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Neumann (1901) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Neumann (1907) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Pavesi (1883) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick et al. (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Plénet (1965) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Ponel et al. (2017) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Rivière (1979) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Rossi & Godoy (2006) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Schicha (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Seurat (1934) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Simon (1864) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1873) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Smit (2002) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Smit (2009) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Staręga (1989) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 0 | 0% |
IOBC-WPRS Bulletin, 18(5): 36-38.">Tamonte (1995) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tentcheva et al. (2004) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Thorell (1875) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Thorell (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier et al. (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Travé (1982) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ueckermann & Loots (1988) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Ueckermann (1992) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Valerio (1981) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal (2012) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Vitzthum (1935) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Walckenaer (1805) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1837) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1837) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Walter (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ythier (2018) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |
Zannou et al. (2007) | 1 | 0,12% | 1 | 0,32% | 1 | 0,33% | 1 | 0,33% |