Crustacés de Guadeloupe
369 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Poupin & Corbari (2016) | 260 | 15,99% | 234 | 30,75% | 234 | 30,91% | 234 | 30,91% |
Poupin (2024) | 196 | 12,05% | 195 | 25,62% | 195 | 25,76% | 195 | 25,76% |
Carmona-Suárez & Poupin (2016) | 119 | 7,32% | 99 | 13,01% | 99 | 13,08% | 99 | 13,08% |
Questel (2020) | 101 | 6,21% | 100 | 13,14% | 100 | 13,21% | 100 | 13,21% |
Tricart & Foubert (2000) | 97 | 5,97% | 72 | 9,46% | 72 | 9,51% | 71 | 9,38% |
Poupin (2018) | 96 | 5,9% | 84 | 11,04% | 84 | 11,1% | 84 | 11,1% |
Poupin (2010) | 81 | 4,98% | 74 | 9,72% | 74 | 9,78% | 74 | 9,78% |
Poupin (1994) | 78 | 4,8% | 62 | 8,15% | 62 | 8,19% | 62 | 8,19% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 69 | 4,24% | 14 | 1,84% | 14 | 1,85% | 14 | 1,85% |
Corbari et al. (2015) | 67 | 4,12% | 57 | 7,49% | 57 | 7,53% | 57 | 7,53% |
Carré (2006) | 52 | 3,2% | 43 | 5,65% | 43 | 5,68% | 43 | 5,68% |
Paulmier (1996) | 42 | 2,58% | 32 | 4,2% | 32 | 4,23% | 32 | 4,23% |
Corbari et al. (2020) | 32 | 1,97% | 22 | 2,89% | 22 | 2,91% | 22 | 2,91% |
Questel & Le Quellec (2012) | 30 | 1,85% | 24 | 3,15% | 24 | 3,17% | 24 | 3,17% |
Poupin & Lemaitre (2014) | 28 | 1,72% | 28 | 3,68% | 28 | 3,7% | 28 | 3,7% |
Kim & Boxshall (2020) | 23 | 1,41% | 21 | 2,76% | 21 | 2,77% | 21 | 2,77% |
Colin (1998) | 19 | 1,17% | 18 | 2,37% | 17 | 2,25% | 18 | 2,38% |
Machordom et al. (2022) | 18 | 1,11% | 18 | 2,37% | 18 | 2,38% | 18 | 2,38% |
Dussart (1982) | 16 | 0,98% | 15 | 1,97% | 11 | 1,45% | 15 | 1,98% |
Guéguen (2000) | 14 | 0,86% | 11 | 1,45% | 11 | 1,45% | 11 | 1,45% |
Kim & Boxshall (2021) | 14 | 0,86% | 14 | 1,84% | 14 | 1,85% | 14 | 1,85% |
Monti et al. (2010) | 14 | 0,86% | 13 | 1,71% | 13 | 1,72% | 13 | 1,72% |
Saussure (1857) | 14 | 0,86% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
UICN Comité français, OFB & MNHN (2021) | 14 | 0,86% | 14 | 1,84% | 14 | 1,85% | 14 | 1,85% |
Lim et al. (2002) | 12 | 0,74% | 12 | 1,58% | 12 | 1,59% | 12 | 1,59% |
Rodríguez-Flores et al. (2018) | 12 | 0,74% | 9 | 1,18% | 9 | 1,19% | 9 | 1,19% |
Beltran (1982) | 10 | 0,62% | 10 | 1,31% | 10 | 1,32% | 10 | 1,32% |
Carvacho (1977) | 9 | 0,55% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Poupin et al. (1999) | 9 | 0,55% | 8 | 1,05% | 8 | 1,06% | 8 | 1,06% |
Rodríguez-Flores et al. (2022) | 9 | 0,55% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Lemaitre et al. (2017) | 8 | 0,49% | 8 | 1,05% | 8 | 1,06% | 8 | 1,06% |
Lucatelli et al. (2012) | 8 | 0,49% | 7 | 0,92% | 7 | 0,92% | 7 | 0,92% |
Rogers et al. (2020) | 8 | 0,49% | 8 | 1,05% | 8 | 1,06% | 8 | 1,06% |
Anker (2012) | 7 | 0,43% | 7 | 0,92% | 7 | 0,92% | 7 | 0,92% |
Coutiere (1909) | 7 | 0,43% | 5 | 0,66% | 5 | 0,66% | 4 | 0,53% |
Crosnier (1976) | 7 | 0,43% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Ifremer (2009) | 7 | 0,43% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Questel (2014) | 7 | 0,43% | 7 | 0,92% | 7 | 0,92% | 7 | 0,92% |
Yokoyama (2013) | 7 | 0,43% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Baba & Wicksten (2017) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Bracken-Grissom & Felder (2014) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Ciavatti (1989) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Lowry (2007) | 6 | 0,37% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Mclaughlin (1981) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Pinheiro & Boos (2016) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Piscart et al. (2019) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Poupin et al. (2013) | 6 | 0,37% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Schotte et al. (1995 onwards) | 6 | 0,37% | 6 | 0,79% | 6 | 0,79% | 6 | 0,79% |
Anker & Baeza (2021) | 5 | 0,31% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Linnaeus (1758) | 5 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Martens & Savatenalinton (2011) | 5 | 0,31% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Miers (1878) | 5 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2017) | 5 | 0,31% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Rodriguez et al. (2019) | 5 | 0,31% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Rojas-Beltran (1981) | 5 | 0,31% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Uicn et al. (2019) | 5 | 0,31% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Ashrafi & Hultgren (2022) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 3 | 0,4% |
Boone (1927) | 4 | 0,25% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chen et al. (2016) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Fiers (1991) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Fourt et al. (2017) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Goulletquer (2016) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Guinot et al. (2018) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Holthuis (1958) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
IUCN (2013) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Kensley (1984) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Lemaitre (2020) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Nobili (1906) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliviera (1939) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Rathbun (1898) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Rigaud et al. (1997) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Stoddart & Lowry (2004) | 4 | 0,25% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Anker & Corbari (2020) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Anker et al. (2012) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Anker (2017) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Chace (1939) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Diaz & Cuzange (2009) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gueguen (1998) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Jackson (1933) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Menzies & Glynn (1968) | 3 | 0,18% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Meurgey (2011) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Questel (2023) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Rathbun (1924) | 3 | 0,18% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Richardson (1914) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Schmitt (1933) | 3 | 0,18% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stimpson (1871) | 3 | 0,18% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stimpson (1871) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Tavares (1994) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Vandel (1981) | 3 | 0,18% | 3 | 0,39% | 3 | 0,4% | 3 | 0,4% |
Anker (2007) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Anker (2014) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Anker (2020) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Balvay (2009) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 1 | 0,13% |
Barnard (1974) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Benedict (1902) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bousfield (1996) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brattegard (1970) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bray et al. (1990) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Burkenroad (1939) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chace (1962) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Churchill (1942) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Colin & Hoibian (2003) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Crane (1943) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Defaye & Dussart (1988) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Farfante & Bullis (1973) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Farfante (1967) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Farfante (1971) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fiers (1990) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Forest & Saint Laurent | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Garcia (1977) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Godet et al. (2010) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Goeke (1989) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gueguen (1995) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gueguen (1997) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Guinot-dumortier (1960) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Hines et al. (1995) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Holthuis (1974) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Jackson (1941) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kensley & Schotte (1994) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Klie (1939) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lecroy (1995) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Leistikow & Wägele (1999) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lemaitre & Campos (1993) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lemaitre & Mclaughlin (1996) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lemaitre (1986) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lucas (1846) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Macia & Robinson (2009) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Macpherson et al. (2016) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Macpherson (1988) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Macpherson (2007) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Manning (1969) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Martens et al. (2019) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Menzies & Glynn (1968) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Milne-edwards (1837) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-Edwards (1881) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1991) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Müller (1993) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Nelson-Smith et al. (2014) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Olivier (1791-[1792]) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
. 34, 293-302">Ortiz & Lalana (1994) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ortiz & Lemaitre (1997) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Patton et al. (1985) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Poupin et al. (2018) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rathbun (1901) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bulletin de la Société Zoologique de France, xxviii: 63-79.">Richard (1903) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Righi (1965) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1816) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Robles et al. (2007) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rodríguez-flores et al. (2018) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Roman-contreras & Bourdon (2001) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Sarver et al. (1998) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmitt (1924) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Shirley & Wolcott (1991) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stock & Vermuelen (1984) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Stock (1980) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Taiti & Ferrara (1983) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Tavares & Melo (2010) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Telford (1980) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Turkay (1975) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Vereshchaka (1994) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
von Hagen (1968) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1904) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wass (1963) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Werding (1996) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Williams & Child (1989) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Williams (1974) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Williamson et al. (2012) | 2 | 0,12% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Abbe (1974) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 69-84.">Agassiz (1880) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ahyong (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Amanieu & Dantec (1961) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Anker & Grave (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Anonyme (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Arnaud (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ary et al. (1985) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Audouin (1826) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Australian Museum (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Barnard (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1954) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bell (1865) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Benedict (1901) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Boone (1918) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Boone (1921) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boone (1930) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousfield (1984) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bouvier (1901) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Comptes rendus hebdomadaires des séances de l'Académie des sciences, 141: 746-749.">Bouvier (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1905) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bouvier (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowman (1979) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brady (1904) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brandt (1833) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bruce (1974) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brumbaugh & Mcconaugha (1995) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Burkenroad (1936) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Burkenroad (1946) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Carbonel et al. (2007) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Carmona-Suarez (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Carmona-Suarez (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Carmona-suarez (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Carvacho (1979) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chace (1969) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Champeau & Thiéry (1990) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Champeau (1967) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Chan (1991) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1887) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1908) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Christoffersen (1979) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ciavatti et al. (1993) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cochard et al. (2010) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coelho (1972) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Costlow et al. (1958) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Costlow (1967) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coulis (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cousins et al. (2013) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
"The Fauna and Geography of the Maldive and Laccadive Archipelagoes" edited by J. Stanley Gardiner, Cambridge, 4to, vol. ii, part 4: 852-921, pls. lxx-lxxxvii, text-figg. 127-139.: 852-921.">Coutiere (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cronin (1949) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Crosnier (1986) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Curd et al. (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Daday (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Daugherty (1952) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Davis et al. (2004) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Delsalle & Sechet (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dewarumez et al. (2011) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dittel et al. (2006) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dollfus (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dussart (1984) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 27: 177-274.">Edwards & Bouvier (1909) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Etcheberry & Abraham (2009) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferguson (1967) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferry et al. (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fingerman (1955) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Forward et al. (2003) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fossati & Marquet (1998) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fransen (1990) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Freeman et al. (1987) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Galil et al. (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Galil (2000) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Garth (1951) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gomez (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gonzalez-ortegon et al. (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Goy (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gray & Newcombe (1938) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Guerne & Richard (1893) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinot (1969) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gunter (1938) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gurney (1943) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Hansen (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Havens et al. (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holmes (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1950) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holthuis (1955) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1960) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holthuis (1962) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Holthuis (1977) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Horeau et al. (2005) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hołyńska & Stoch (2011) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Huff (1979) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Impact-Mer et al. (2011) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ives (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jackson (1933) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Jackson (1938) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Johnson (1867) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones (1969) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kim & Boxshall (2021) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kingsley (1878) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Klie (1939) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Knowlton & Keller (1983) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Labrune et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legrand (1949) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1953) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenz & Strunck (1914) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Li (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lochhead & Newcombe (1942) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Macia & Robinson (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Macpherson & Segonzac (2005) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mancinelli et al. (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mancinelli et al. (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Manning & Holthuis (1989) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mckinney (1980) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Méhes (1939) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisch et al. (2007) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Meisch et al. (2019) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Michel-Salzat & Bouchon (2000) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Miers (1879) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1881) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Milne-edwards & Bouvier (1897) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-edwards (1873-1880) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Milne-Edwards (1878) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Milne-edwards (1883) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Milne-Edwards (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1986) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Müller (1991) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Müller (1993) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mulochau et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Proceedings of the Hawaiian Entomological Society, 9(1): 69-70.">Mumford (1935) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Myers (1989) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Newcombe et al. (1949) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Nobili (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Boulad (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël & Prouzet (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Noël (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pachelle et al. (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Packard (1871) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Peart & Hughes (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pêpe et al. (2021) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pezy et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pfaller et al. (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Poisson & Legueux (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Poore (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Poupin & Felder (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Poupin et al. (2013) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabet et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rathbun (1892) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1896) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rathbun (1934) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rehberg (1880) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Renon & Lefèvre (1985) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Richard (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1897) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Righi (1967) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rios & Duffy (2007) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roudez et al. (2008) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Roy (1922) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ryer et al. (1997) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sadek et al. (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sanchez (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sandoz & Rogers (1944) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schabetsberger et al. (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schellenberg (1938) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt et al. (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schmitt (1939) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Séchet et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stephensen (1935) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stimpson (1860) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stout (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Suárez-Morales et al. (2006) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tavares & Amouroux (2003) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tavares & Gouvea (2013) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Thongda et al. (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tollu (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Torres et al. (2006) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vereshchaka et al. (2020) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Verhoeff (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincent (1986) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Weckel (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Weissburg & Zimmer-faust (1994) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Werding (1982) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wolcott et al. (2005) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Yang et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
(1967) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |