Hémiptères de la Réunion
283 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Matile-Ferrero & Etienne (2006) | 117 | 13,37% | 115 | 25,39% | 115 | 25,84% | 115 | 25,84% |
Meurgey & Ramage (2020) | 106 | 12,11% | 104 | 22,96% | 104 | 23,37% | 104 | 23,37% |
Legros et al. (2017) | 101 | 11,54% | 94 | 20,75% | 93 | 20,9% | 92 | 20,67% |
Meurgey (2011) | 97 | 11,09% | 92 | 20,31% | 92 | 20,67% | 92 | 20,67% |
Germain et al. (2014) | 90 | 10,29% | 89 | 19,65% | 89 | 20% | 89 | 20% |
Bonfils et al. (1994) | 83 | 9,49% | 82 | 18,1% | 80 | 17,98% | 82 | 18,43% |
Vayssières et al. (2001) | 83 | 9,49% | 78 | 17,22% | 78 | 17,53% | 76 | 17,08% |
Ramage (2017) | 78 | 8,91% | 77 | 17% | 77 | 17,3% | 77 | 17,3% |
Jourdan & Mille (2006) | 65 | 7,43% | 61 | 13,47% | 61 | 13,71% | 61 | 13,71% |
Mille et al. (2016) | 61 | 6,97% | 60 | 13,25% | 60 | 13,48% | 60 | 13,48% |
Etienne (2005) | 48 | 5,49% | 45 | 9,93% | 45 | 10,11% | 45 | 10,11% |
Remaudière & Etienne (1988) | 46 | 5,26% | 42 | 9,27% | 42 | 9,44% | 42 | 9,44% |
Foldi & Germain (2018) | 40 | 4,57% | 39 | 8,61% | 39 | 8,76% | 39 | 8,76% |
Germain (2007) | 38 | 4,34% | 38 | 8,39% | 38 | 8,54% | 38 | 8,54% |
Nibouche et al. (202X) | 28 | 3,2% | 27 | 5,96% | 26 | 5,84% | 27 | 6,07% |
Remillet (1988) | 28 | 3,2% | 19 | 4,19% | 19 | 4,27% | 19 | 4,27% |
Etienne & Vilardebó (1978) | 27 | 3,09% | 24 | 5,3% | 24 | 5,39% | 24 | 5,39% |
Streito et al. (2007) | 27 | 3,09% | 25 | 5,52% | 25 | 5,62% | 25 | 5,62% |
Mille et al. (2020) | 24 | 2,74% | 23 | 5,08% | 23 | 5,17% | 23 | 5,17% |
Jourdan (2020) | 20 | 2,29% | 19 | 4,19% | 19 | 4,27% | 19 | 4,27% |
Anonyme (2018) | 19 | 2,17% | 19 | 4,19% | 19 | 4,27% | 19 | 4,27% |
Votýpka et al. (2020) | 18 | 2,06% | 17 | 3,75% | 14 | 3,15% | 17 | 3,82% |
Cochereau (1966) | 17 | 1,94% | 17 | 3,75% | 17 | 3,82% | 17 | 3,82% |
Cohic (1959) | 17 | 1,94% | 13 | 2,87% | 13 | 2,92% | 13 | 2,92% |
Matile-Ferrero (1979) | 14 | 1,6% | 14 | 3,09% | 14 | 3,15% | 14 | 3,15% |
Paulian (1998) | 14 | 1,6% | 13 | 2,87% | 13 | 2,92% | 13 | 2,92% |
Williams (1976) | 14 | 1,6% | 14 | 3,09% | 14 | 3,15% | 14 | 3,15% |
Russell & Etienne (1985) | 13 | 1,49% | 13 | 2,87% | 13 | 2,92% | 13 | 2,92% |
Attié et al. (2002) | 12 | 1,37% | 12 | 2,65% | 12 | 2,7% | 12 | 2,7% |
Drake (1957) | 12 | 1,37% | 10 | 2,21% | 10 | 2,25% | 10 | 2,25% |
Lagarde (2008) | 12 | 1,37% | 12 | 2,65% | 12 | 2,7% | 11 | 2,47% |
Questel (2020) | 12 | 1,37% | 12 | 2,65% | 12 | 2,7% | 12 | 2,7% |
Cochereau (1974) | 11 | 1,26% | 11 | 2,43% | 11 | 2,47% | 11 | 2,47% |
Gutierrez (1981) | 11 | 1,26% | 8 | 1,77% | 8 | 1,8% | 8 | 1,8% |
Hullé et al. (2018) | 10 | 1,14% | 10 | 2,21% | 10 | 2,25% | 10 | 2,25% |
Linnaeus (1758) | 10 | 1,14% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Matile-Ferrero et al. (2000) | 9 | 1,03% | 9 | 1,99% | 9 | 2,02% | 9 | 2,02% |
Questel & Le Quellec (2012) | 9 | 1,03% | 9 | 1,99% | 9 | 2,02% | 9 | 2,02% |
Mamet (1959) | 8 | 0,91% | 8 | 1,77% | 8 | 1,8% | 8 | 1,8% |
Dominique (1892) | 7 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Dusoulier (2015) | 7 | 0,8% | 7 | 1,55% | 7 | 1,57% | 7 | 1,57% |
Matile-Ferrero & Williams (2015) | 7 | 0,8% | 7 | 1,55% | 7 | 1,57% | 7 | 1,57% |
Attié et al. (1998) | 6 | 0,69% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Bonfils et al. (2001) | 6 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonfils (1993) | 6 | 0,69% | 6 | 1,32% | 6 | 1,35% | 6 | 1,35% |
Germain (2013) | 6 | 0,69% | 6 | 1,32% | 6 | 1,35% | 6 | 1,35% |
Quilici et al. (1988) | 6 | 0,69% | 6 | 1,32% | 6 | 1,35% | 6 | 1,35% |
Wygodzinsky (1966) | 6 | 0,69% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Attié et al. (2008) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Cheesman (1927) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Frenot et al. (2005) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Hullé & Vernon (2021) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Klyver (1932) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Mifsud et al. (2010) | 5 | 0,57% | 5 | 1,1% | 5 | 1,12% | 5 | 1,12% |
Montrouzier (1861) | 5 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Benfatti et al. (2008) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Dadant & Etienne (1973) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Dominique (1902) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 4 | 0,46% | 4 | 0,88% | 3 | 0,67% | 4 | 0,9% |
Garrouste & Hervé (2009) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Haupt (1927) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodkinson (1983) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Hullé et al. (2003) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Hullé et al. (2010) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Mckamey (2010) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Putshkov et al. (1999) | 4 | 0,46% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Román-Palacios et al. (2020) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Van Duzee (1937) | 4 | 0,46% | 4 | 0,88% | 4 | 0,9% | 4 | 0,9% |
Albouy et al. (2017) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Boulard (1989) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Carayon (1958) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Della & Giustina (2019) | 3 | 0,34% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Etienne & Champoiseau (2011) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Fennah (1969) | 3 | 0,34% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Gnezdilov & Bartlett (2022) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Hoch et al. (2003) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Knight (1987) | 3 | 0,34% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Kormilev (1971) | 3 | 0,34% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kozár (2004) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Lupoli (2023) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Matocq et al. (2019) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Matocq et al. (2020) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Mollot et al. (2016) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Ouvrard et al. (2016) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Poisson (1957) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Richard (1980) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Schouteden (1907) | 3 | 0,34% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Stehlik (2013) | 3 | 0,34% | 3 | 0,66% | 3 | 0,67% | 3 | 0,67% |
Asche & Wilson (1990) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Bonfils & Attie (1998) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Borowiec et al. (2010) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Cairaschi (1941) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Carayon (1957) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Carpintero & Dellapé (2006) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Carpintero (2002) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Cesne et al. (2022) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Cockerell (1893) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1950) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Couteyen (2004) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Damgaard & Zettel (2014) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Distant (1914) | 2 | 0,23% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Drake & Hambleton (1946) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Drake & Livingstone (1964) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Drake & Mamet (1956) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Duay et al. (2014) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Dumbleton (1956) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2001) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Ezzat (1958) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Fabricius (1803) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1958) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Ferris (1935) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Germain & Streito (2004) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Gnezdilov (2009) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Guilbert (2002) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Hammes & Putoa (1986) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Hartmann et al. (2021) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Heiss (2011) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Hempel (1902) | 2 | 0,23% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Horváth (1914) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Knight (2010) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Kreiter et al. (2022) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Lethierry (1881) | 2 | 0,23% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Mamet (1937) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Mamet (1939) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquereau et al. (2022) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Martoni & Brown (2018) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Maskell (1893) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Matile-Ferrero & Etienne (1996) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Matile-Ferrero & Etienne (1998) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Matocq et al. (2017) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Morgan (1889) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Newstead (1908) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Revista de Entomologia de Mozambique, 4: 1-35.">Odhiambo (1961) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Olivier (1791-[1792]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Osborn (1934) | 2 | 0,23% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Panis (1969) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Percy (2017) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Poisson (1945) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Postle (2018) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Quilici et al. (1998) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Russell (1965) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Samy (1969) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Scopoli (1763) | 2 | 0,23% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Streito et al. (2018) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Takahashi (1938) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Takahashi (1960) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Taquet et al. (2019) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Vayssières et al. (2017) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Villiers (1976) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang et al. (2021) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Williams & Watson (1988) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2023) | 2 | 0,23% | 2 | 0,44% | 2 | 0,45% | 2 | 0,45% |
Amyot & Audinet-Serville (1843) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Anonyme (2023) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Asche (1980) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Baena (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Balachowsky (1958) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Béguinot (2012) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ben-Dov et al. (2000) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Berenger & Pluot-Sigwalt (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bergroth (1893) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bigot (1992) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Biondi et al. (2013) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bondar (1923) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgoin (1997) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bout et al. (2021) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Boyer de Fonscolombe (1834) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Brain (1920) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Buchanan & White (1879) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Burmeister (1835) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cahuzac & Dauphin (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Callot (2021) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Chapelin-viscardi & Binon (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Chebbah et al. (2021) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Chebbah et al. (2023) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Chérot & Carpintero (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cherot & Carpintero (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cochard et al. (2021) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cochereau (1966) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cockerell (1901) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Colligros & Lebecque (2012) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Couteyen (2006) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Dauphin & Matile-Ferrero (2003) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
De Geer (1773) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Della Giustina & Remane (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Disney & Chazeau (1990) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Dispons (1965) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Distant (1913) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Distant (1920) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Dmitriev (2020) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Drake (1922) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbleton (1961) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Dupuis (1999) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Duquef (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Duquef (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Durai (1987) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Elder (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Elder (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etcheberry & Abraham (2009) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etienne et al. (1998) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etienne et al. (1998) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etienne (1978) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etienne (1978) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Eyles (1999) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Fabres (1977) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Fabricius (1775) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1963) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste (2015) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Germain & Chapin (2004) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Germain et al. (2007) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Germain et al. (2014) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Germar (1821) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Goux (1937) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Green (1896) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert (2008) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Hausmann (1802) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hempel (1901) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hempel (1922) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Horvàth (1895) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Hulle et al. (1996) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Hungerford & Evans (1934) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Jurberg et al. (2015) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kaltenbach (1843) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kóbor & Kondorosy (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kóbor (2023) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kormilev (1965) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1801) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Languillon (1951) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Leavengood et al. (2024) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lotto (1975) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lowe et al. (2007) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lucas (1872) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Luziau (1953) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Malausa & Ehanno (1988) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mamet (1942) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Mary (2017) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Matile-Ferrero & Germain (2004) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Matocq & Streito (2013) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Matsumura (1912) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Metcalf (1955) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1855) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1858) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mound & Halsey (1978) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Newstead (1909) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nielson (1982) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ouvrard et al. (2015) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Péricart (1981) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Piednoir et al. (2020) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Plénet (1965) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Poisson (1957) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Polhemus & Herring (1970) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Polhemus & Martiré (2014) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Poppius (1920) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Putshkov & Moulet (2010) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Putshkov (1987) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Quaintance (1903) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1959) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ramage et al. (2023) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ratnadass et al. (2018) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Robert (1969) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Rosa et al. (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Sauvion et al. (1999) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Streito et al. (2016) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Streito et al. (2023) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Takahashi (1955) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Touroult et al. (2018) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Tuthill (1942) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Tuthill (1955) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Unruh & Gullan (2008) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandeschricke et al. (1992) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Villiers (1951) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Villiers (1962) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson et al. (2015) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2001) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Williams et al. (2006) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Williams (1961) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wondafrash et al. (2020) | 1 | 0,11% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Yokoyama (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |