Arachnides de Nouvelle-Calédonie
380 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Platnick (1993) | 191 | 14,75% | 155 | 20,81% | 153 | 20,76% | 155 | 21% |
Berland (1924) | 157 | 12,12% | 98 | 13,15% | 98 | 13,3% | 97 | 13,14% |
Ramage (2017) | 81 | 6,25% | 73 | 9,8% | 69 | 9,36% | 70 | 9,49% |
Smit (2002) | 65 | 5,02% | 53 | 7,11% | 53 | 7,19% | 53 | 7,18% |
Karg (1996) | 63 | 4,86% | 55 | 7,38% | 55 | 7,46% | 55 | 7,45% |
Jourdan (2020) | 53 | 4,09% | 50 | 6,71% | 47 | 6,38% | 49 | 6,64% |
Raven (1994) | 49 | 3,78% | 49 | 6,58% | 49 | 6,65% | 49 | 6,64% |
Raven & Churchill (1991) | 43 | 3,32% | 43 | 5,77% | 43 | 5,83% | 43 | 5,83% |
Smit (2009) | 43 | 3,32% | 40 | 5,37% | 40 | 5,43% | 40 | 5,42% |
Migeon (2015) | 41 | 3,17% | 41 | 5,5% | 41 | 5,56% | 41 | 5,56% |
Jourdan & Mille (2006) | 39 | 3,01% | 36 | 4,83% | 36 | 4,88% | 36 | 4,88% |
Balogh & Balogh (1983) | 36 | 2,78% | 33 | 4,43% | 33 | 4,48% | 33 | 4,47% |
Berland (1929) | 35 | 2,7% | 19 | 2,55% | 19 | 2,58% | 18 | 2,44% |
Berland (1933) | 32 | 2,47% | 14 | 1,88% | 14 | 1,9% | 13 | 1,76% |
Ermilov & Mary (2020) | 31 | 2,39% | 31 | 4,16% | 28 | 3,8% | 30 | 4,07% |
Karg (1993) | 30 | 2,32% | 30 | 4,03% | 30 | 4,07% | 30 | 4,07% |
Kury et al. (2024) | 30 | 2,32% | 30 | 4,03% | 30 | 4,07% | 30 | 4,07% |
Baehr et al. (2013) | 28 | 2,16% | 28 | 3,76% | 28 | 3,8% | 28 | 3,79% |
Berland (1934) | 27 | 2,08% | 13 | 1,74% | 13 | 1,76% | 11 | 1,49% |
Karg (1993) | 26 | 2,01% | 24 | 3,22% | 24 | 3,26% | 24 | 3,25% |
Niedbała & Penttinen (2007) | 26 | 2,01% | 17 | 2,28% | 17 | 2,31% | 17 | 2,3% |
Raven (1991) | 26 | 2,01% | 26 | 3,49% | 26 | 3,53% | 26 | 3,52% |
Berland (1934) | 24 | 1,85% | 13 | 1,74% | 13 | 1,76% | 11 | 1,49% |
Bigot (1992) | 22 | 1,7% | 15 | 2,01% | 15 | 2,04% | 13 | 1,76% |
Niedbała (2000) | 22 | 1,7% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Berlese (1923) | 20 | 1,54% | 10 | 1,34% | 10 | 1,36% | 10 | 1,36% |
Dierkens & Charlat (2011) | 20 | 1,54% | 15 | 2,01% | 15 | 2,04% | 14 | 1,9% |
Karg (1997) | 20 | 1,54% | 18 | 2,42% | 18 | 2,44% | 18 | 2,44% |
Delfosse (2017) | 19 | 1,47% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Sharma & Giribet (2009) | 19 | 1,47% | 19 | 2,55% | 19 | 2,58% | 19 | 2,57% |
Hammes & Putoa (1986) | 18 | 1,39% | 18 | 2,42% | 18 | 2,44% | 18 | 2,44% |
Meurgey (2011) | 18 | 1,39% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Subías (2004) | 17 | 1,31% | 16 | 2,15% | 15 | 2,04% | 15 | 2,03% |
Berland (1942) | 16 | 1,24% | 9 | 1,21% | 9 | 1,22% | 7 | 0,95% |
Cazanove (2022) | 16 | 1,24% | 14 | 1,88% | 14 | 1,9% | 13 | 1,76% |
Delfosse (2024) | 16 | 1,24% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Kontschán (2013) | 16 | 1,24% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Patoleta et al. (2017) | 16 | 1,24% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Shear (1993) | 16 | 1,24% | 16 | 2,15% | 16 | 2,17% | 16 | 2,17% |
Flechtmann et al. (1999) | 15 | 1,16% | 15 | 2,01% | 15 | 2,04% | 15 | 2,03% |
Kreiter et al. (2020) | 15 | 1,16% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Rageau (1958) | 15 | 1,16% | 12 | 1,61% | 12 | 1,63% | 12 | 1,63% |
Simon (1897) | 15 | 1,16% | 6 | 0,81% | 6 | 0,81% | 5 | 0,68% |
De Moraes et al. (2016) | 14 | 1,08% | 13 | 1,74% | 13 | 1,76% | 13 | 1,76% |
Dierkens & Ramage (2016) | 14 | 1,08% | 12 | 1,61% | 12 | 1,63% | 10 | 1,36% |
Ledoux & Hallé (1995) | 14 | 1,08% | 8 | 1,07% | 8 | 1,09% | 8 | 1,08% |
Niedbała (1998) | 14 | 1,08% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Berland (1935) | 13 | 1% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Walter (1915) | 13 | 1% | 12 | 1,61% | 12 | 1,63% | 12 | 1,63% |
Dierkens (2021) | 12 | 0,93% | 12 | 1,61% | 12 | 1,63% | 10 | 1,36% |
Giribet et al. (2021) | 12 | 0,93% | 12 | 1,61% | 12 | 1,63% | 12 | 1,63% |
Patoleta (2016) | 12 | 0,93% | 11 | 1,48% | 11 | 1,49% | 11 | 1,49% |
Berlese (1910) | 11 | 0,85% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Guglielmone et al. (2023) | 11 | 0,85% | 11 | 1,48% | 11 | 1,49% | 11 | 1,49% |
Hammer (1972) | 11 | 0,85% | 10 | 1,34% | 8 | 1,09% | 9 | 1,22% |
Makol (2009) | 11 | 0,85% | 11 | 1,48% | 11 | 1,49% | 11 | 1,49% |
Niedbała & Liu (2023) | 11 | 0,85% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Platnick & Forster (1993) | 11 | 0,85% | 11 | 1,48% | 11 | 1,49% | 11 | 1,49% |
Beier (1966) | 10 | 0,77% | 8 | 1,07% | 8 | 1,09% | 8 | 1,08% |
Gray (1992) | 10 | 0,77% | 10 | 1,34% | 10 | 1,36% | 10 | 1,36% |
Gutierrez (1979) | 10 | 0,77% | 10 | 1,34% | 10 | 1,36% | 10 | 1,36% |
Gutierrez (1981) | 10 | 0,77% | 9 | 1,21% | 9 | 1,22% | 9 | 1,22% |
Patoleta (2014) | 10 | 0,77% | 10 | 1,34% | 10 | 1,36% | 10 | 1,36% |
Rageau (1959) | 10 | 0,77% | 9 | 1,21% | 7 | 0,95% | 9 | 1,22% |
Seeman (2022) | 10 | 0,77% | 10 | 1,34% | 10 | 1,36% | 10 | 1,36% |
Weygoldt (2006) | 10 | 0,77% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Beier (1964) | 9 | 0,69% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Berry et al. (1997) | 9 | 0,69% | 9 | 1,21% | 9 | 1,22% | 9 | 1,22% |
Brun et al. (1983) | 9 | 0,69% | 9 | 1,21% | 9 | 1,22% | 9 | 1,22% |
Colloff (2012) | 9 | 0,69% | 9 | 1,21% | 9 | 1,22% | 9 | 1,22% |
Ermilov et al. (2013) | 9 | 0,69% | 9 | 1,21% | 9 | 1,22% | 8 | 1,08% |
Vedel et al. (2013) | 9 | 0,69% | 9 | 1,21% | 9 | 1,22% | 8 | 1,08% |
Flechtmann et al. (2000) | 8 | 0,62% | 8 | 1,07% | 8 | 1,09% | 8 | 1,08% |
Patoleta & Żabka (2019) | 8 | 0,62% | 8 | 1,07% | 8 | 1,09% | 8 | 1,08% |
Sellnick (1959) | 8 | 0,62% | 7 | 0,94% | 6 | 0,81% | 7 | 0,95% |
Berry et al. (1996) | 7 | 0,54% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Castilho et al. (2016) | 7 | 0,54% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Jacot (1934) | 7 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick (2002) | 7 | 0,54% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Pocock (1898) | 7 | 0,54% | 5 | 0,67% | 5 | 0,68% | 4 | 0,54% |
Questel (2020) | 7 | 0,54% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Souza et al. (2019) | 7 | 0,54% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Vayssières et al. (2001) | 7 | 0,54% | 7 | 0,94% | 7 | 0,95% | 7 | 0,95% |
Baehr & Harvey (2013) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Berlese (1918) | 6 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 5 | 0,68% |
Ermilov & Mary (2019) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 5 | 0,68% |
Fain & Aellen (1994) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Gutierrez & Etienne (1986) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Ifremer (2009) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Karg (1995) | 6 | 0,46% | 6 | 0,81% | 6 | 0,81% | 6 | 0,81% |
Kreiter & Moraes (1997) | 6 | 0,46% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Marples (1957) | 6 | 0,46% | 4 | 0,54% | 4 | 0,54% | 3 | 0,41% |
Nentwig et al. (2019) | 6 | 0,46% | 5 | 0,67% | 5 | 0,68% | 4 | 0,54% |
Rageau (1956) | 6 | 0,46% | 4 | 0,54% | 2 | 0,27% | 4 | 0,54% |
Simon (1880) | 6 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 6 | 0,46% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Delfosse (2018) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Dupérré (2023) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Etienne & Vilardebó (1978) | 5 | 0,39% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Giribet et al. (2021) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Gutierrez (1968) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Kallal & Hormiga (2018) | 5 | 0,39% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Kraepelin (1914) | 5 | 0,39% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Kreiter et al. (2002) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Pritchard & Baker (1955) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Questel & Le Quellec (2012) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Quilici et al. (2000) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Taczanowski (1874) | 5 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 5 | 0,39% | 5 | 0,67% | 5 | 0,68% | 5 | 0,68% |
Colloff (2023) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Flechtmann & Etienne (2000) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Jacot (1934) | 4 | 0,31% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Karg (1997) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Koch (1867) | 4 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Kreiter et al. (2018) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Kury & Machado (2009) | 4 | 0,31% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Lehtinen (1995) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Magalhaes et al. (2022) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Mahunka & Mahunka-Papp (1995) | 4 | 0,31% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Mahunka (1991) | 4 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin & Smit (2002) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Miranda et al. (2021) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Nava et al. (2018) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Niedbała (1993) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Pešić et al. (2021) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Raven (2015) | 4 | 0,31% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Roewer (1914) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Schicha (1979) | 4 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Schicha (1981) | 4 | 0,31% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Schicha (1984) | 4 | 0,31% | 4 | 0,54% | 4 | 0,54% | 4 | 0,54% |
Adamson (1935) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Atyeo & Gaud (1992) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Atyeo & Peterson (1992) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Balogh (1978) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Beatty et al. (2008) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Beier (1968) | 3 | 0,23% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Berland (1927) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 2 | 0,27% |
Beron (2021) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Berry et al. (1998) | 3 | 0,23% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Brignoli (1981) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Coineau et al. (1967) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Colloff (2013) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Fain (1991) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Fauvel (1865) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Flechtmann & Etienne (2005) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Flechtmann & Etienne (2006) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Haas et al. (2015) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 0 | 0% |
Hammer (1973) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Karg (1997) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Klein et al. (1982) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Kreiter et al. (2020) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Linnaeus (1758) | 3 | 0,23% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Liu & Zhang (2014) | 3 | 0,23% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Lourenço (2023) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
McGregor (1949) | 3 | 0,23% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
McGregor (1950) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Navajas et al. (2010) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Patoleta (2009) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Quilici et al. (1997) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Rivière (1979) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 2 | 0,27% |
Rix & Harvey (2010) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Roger (2018) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Schicha & Gutierrez (1985) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Schicha (1981) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Seeman (2017) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Simon (1906) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Southcott (1966) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Szuts (2002) | 3 | 0,23% | 3 | 0,4% | 3 | 0,41% | 3 | 0,41% |
Taczanowski (1871) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Alvarez-padilla et al. (2020) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Anonyme (2018) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Aoki (1959) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Atyeo & Gaud (1978) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Banks (1900) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré et al. (2001) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1995) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch (1999) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Beier (1979) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Berlese (1916) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchard (1939) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Brignoli (1980) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Chant & Mcmurtry (2006) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chevalier & Dewynter (2020) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Chrysanthus et al. (1929) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Churchill & Raven (1992) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Cohic (1959) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Coineau et al. (1978) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Cook (1986) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Courtial (2023) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Csiszar (1961) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 0 | 0% |
Dabert et al. (2008) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Dadant & Etienne (1973) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
De Geer (1778) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Enders (1993) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Ermilov & Anichkin (2010) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Esyunin & Zamani (2020) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Fain & Schuster (1984) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Fain (1976) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fan & George (2020) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Flechtmann & Etienne (2001) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Flechtmann et al. (1999) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Gaud & Barré (1988) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Gaud & Barré (1992) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Grandjean (1959) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Gutierrez & Bolland (1981) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Harvey et al. (2007) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Harvey (1989) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Harvey (1990) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Harvey (2009) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Harvey (2020) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Hervé & Garrouste (2009) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Huber (2000) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Hullé et al. (2018) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Karg (1997) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Klompen (1992) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Knihinicki & Boczek (2002) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Koch (1871) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Kreiter & Douin (2021) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Kuntner et al. (2018) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Ledoux (2007) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lions (1966) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Lourenço (1987) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Lucas et al. (208-212) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lundblad (1948) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Ma et al. (2019) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Mahunka (1982) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 1 | 0,14% |
Mahunka (1992) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Migeon et al. (2019) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Moraza et al. (2009) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Muma (1955) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz-Leal et al. (2017) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Neumann (1901) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Niedbała & Colloff (1997) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Niedbała & Corpuz-Raros (1998) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Niedbała (1981) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Niedbała (1997) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Niedbała (2017) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Olszanowski (1997) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Patoleta & Gardzińska (2013) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Patrick (2015) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Pesic & Smit (2007) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Platnick & Baehr, 2006 | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick & Dupérré (2009) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Platnick et al. (2012) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Rageau & Vervent (1959) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Robin & Megnin (1877) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Schrank (1781) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharma & Giribet (2005) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Shiba (1976) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Smit & Gerecke (2010) | 2 | 0,15% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Smit (2015) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Smith (2006) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Taczanowski (1872) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Taczanowski (1874) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Tenorio (1976) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Thibaud & Coineau (1998) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Thorell (1875) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorell (1887) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Trouessart (1899) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Uchikawa (1985) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Vachon (1976) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
Walckenaer ([1841]) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Zabka (1992) | 2 | 0,15% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
André (1938) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Aoki (1965) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Aoki (1994) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Audouin (1826) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Auger et al. (2023) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Baker & Pritchard (1960) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Banks (1905) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré & Camus (1983) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Berlese (1913) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Beron (2020) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Binetruy et al. (2019) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Blommers (1974) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Cazanove (2019) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Chant & Mcmurtry (2004) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Cooreman (1959) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Corpuz-Raros (1995) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Coulis (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
De Azevedo et al. (2019) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
De Moraes et al. (2022) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Déjean & Danflous (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Déjean et al. (2023) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dhondt (2005) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Doleschall (1857) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dosse (1958) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
D'souza & Jagannath (1982) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Dufour (1831) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehara & Amano (2004) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Eldin et al. (2011) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Ermilov & Stary (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Ermilov et al. (2012) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Ewing (1909) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fain & Pauly (2001) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Flechtmann & Etienne (2002) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Fourcroy (1785) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fueßlin (1775) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuller (1899) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gasnier et al. (2015) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Geijskes (1939) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean (1930) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Grandjean (1933) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Gupta (1980) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hacala et al. (2024) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hammer (1967) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hammer (1972) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hammer (1979) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Harvey et al. (2007) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hentz (1847) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hirst & Hirst (1910) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hüe et al. (2021) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Hullé & Vernon (2021) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Jacot (1935) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jacquot et al. (2016) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Jäger (2002) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Keyserling (1865) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Keyserling (1887) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1836) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1872) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kovařík (2003) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Kritscher (1966) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamontellerie (1965) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Latreille (1806) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1807) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Levi (1983) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Liu et al. (2009) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourenço (1983) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Lundblad (1941) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Mašán (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Mahunka (1985) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 0 | 0% |
Mahunka (1988) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Makol & Wohltmann (2012) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Mammola & Milano (2019) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Iinuma (2013) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Marie & Vetter (2015) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Marples (1964) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Moniez (1898-1899) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod (2011) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Morais et al. (2016) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Moreira et al. (2014) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Nentwig & Kobelt (2010) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Neumann (1907) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Niedbała & Starý (2015) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Niedbała (2007) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Oudemans (1923) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Pickard-cambridge (1877) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Ponel et al. (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Pritchard & Baker (1958) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1960) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Raven (1981) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Robson (1878) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi & Godoy (2006) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Roy et al. (2009) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sautet (1936) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sayed (1946) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Schicha (1987) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Seurat (1934) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Sherwood (2022) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Simon (1864) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1889) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1983) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Smit et al. (2023) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Smith et al. (2017) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Subías (2022) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
IOBC-WPRS Bulletin, 18(5): 36-38.">Tamonte (1995) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorell (1870) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorell (1897) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier et al. (2013) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Touroult et al. (2020) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Vinson (1863) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Wada (1967) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Walckenaer (1837) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Warburton (1933) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Woolley (1965) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |
Ythier (2018) | 1 | 0,08% | 1 | 0,13% | 1 | 0,14% | 1 | 0,14% |