Hémiptères de Guadeloupe
295 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Meurgey & Ramage (2020) | 382 | 38,05% | 367 | 76,3% | 362 | 76,37% | 366 | 77,05% |
Meurgey (2011) | 300 | 29,88% | 266 | 55,3% | 262 | 55,27% | 264 | 55,58% |
Matile-Ferrero & Etienne (2006) | 224 | 22,31% | 214 | 44,49% | 208 | 43,88% | 210 | 44,21% |
Lupoli (2023) | 116 | 11,55% | 114 | 23,7% | 114 | 24,05% | 114 | 24% |
Lethierry (1881) | 77 | 7,67% | 25 | 5,2% | 25 | 5,27% | 25 | 5,26% |
Ramage (2017) | 70 | 6,97% | 69 | 14,35% | 68 | 14,35% | 66 | 13,89% |
Etienne (2005) | 62 | 6,18% | 59 | 12,27% | 59 | 12,45% | 59 | 12,42% |
Jourdan & Mille (2006) | 60 | 5,98% | 56 | 11,64% | 56 | 11,81% | 52 | 10,95% |
Streito et al. (2007) | 59 | 5,88% | 57 | 11,85% | 57 | 12,03% | 57 | 12% |
Mille et al. (2016) | 54 | 5,38% | 53 | 11,02% | 53 | 11,18% | 49 | 10,32% |
Germain et al. (2014) | 50 | 4,98% | 50 | 10,4% | 50 | 10,55% | 48 | 10,11% |
Foldi & Germain (2018) | 47 | 4,68% | 45 | 9,36% | 45 | 9,49% | 41 | 8,63% |
Remillet (1988) | 47 | 4,68% | 33 | 6,86% | 33 | 6,96% | 30 | 6,32% |
Germain (2007) | 46 | 4,58% | 46 | 9,56% | 46 | 9,7% | 42 | 8,84% |
Anonyme (2018) | 36 | 3,59% | 35 | 7,28% | 34 | 7,17% | 35 | 7,37% |
Vayssières et al. (2001) | 28 | 2,79% | 25 | 5,2% | 25 | 5,27% | 24 | 5,05% |
Questel (2020) | 27 | 2,69% | 25 | 5,2% | 25 | 5,27% | 25 | 5,26% |
Remaudière & Etienne (1988) | 23 | 2,29% | 21 | 4,37% | 21 | 4,43% | 21 | 4,42% |
Etienne & Vilardebó (1978) | 22 | 2,19% | 20 | 4,16% | 20 | 4,22% | 17 | 3,58% |
Cochereau (1966) | 19 | 1,89% | 19 | 3,95% | 19 | 4,01% | 18 | 3,79% |
Mille et al. (2020) | 19 | 1,89% | 18 | 3,74% | 18 | 3,8% | 18 | 3,79% |
Villiers (1979) | 17 | 1,69% | 12 | 2,49% | 11 | 2,32% | 12 | 2,53% |
Cohic (1959) | 16 | 1,59% | 13 | 2,7% | 13 | 2,74% | 11 | 2,32% |
Heiss (2019) | 16 | 1,59% | 16 | 3,33% | 16 | 3,38% | 16 | 3,37% |
Questel & Le Quellec (2012) | 15 | 1,49% | 13 | 2,7% | 13 | 2,74% | 13 | 2,74% |
Jourdan (2020) | 13 | 1,29% | 13 | 2,7% | 13 | 2,74% | 13 | 2,74% |
Kormilev & Froeschner (1987) | 13 | 1,29% | 13 | 2,7% | 13 | 2,74% | 13 | 2,74% |
Labat (2023) | 13 | 1,29% | 12 | 2,49% | 12 | 2,53% | 12 | 2,53% |
Touroult et al. (2018) | 13 | 1,29% | 13 | 2,7% | 13 | 2,74% | 13 | 2,74% |
Matile-Ferrero (1979) | 12 | 1,2% | 12 | 2,49% | 12 | 2,53% | 11 | 2,32% |
Paulian (1998) | 12 | 1,2% | 11 | 2,29% | 11 | 2,32% | 11 | 2,32% |
Carmen Coscaron (1983) | 11 | 1,1% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Eger (1978) | 11 | 1,1% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Gutierrez (1981) | 11 | 1,1% | 9 | 1,87% | 9 | 1,9% | 9 | 1,89% |
Linnaeus (1758) | 11 | 1,1% | 1 | 0,21% | 1 | 0,21% | 0 | 0% |
Nibouche et al. (202X) | 11 | 1,1% | 11 | 2,29% | 11 | 2,32% | 10 | 2,11% |
Yokoyama (2013) | 11 | 1,1% | 10 | 2,08% | 10 | 2,11% | 10 | 2,11% |
Carpintero (2002) | 10 | 1% | 10 | 2,08% | 10 | 2,11% | 10 | 2,11% |
de Kort-Gommers & Nieser (1969) | 10 | 1% | 10 | 2,08% | 10 | 2,11% | 10 | 2,11% |
Hullé et al. (2018) | 10 | 1% | 10 | 2,08% | 10 | 2,11% | 10 | 2,11% |
Cochereau (1974) | 9 | 0,9% | 9 | 1,87% | 9 | 1,9% | 8 | 1,68% |
Matile-Ferrero et al. (2000) | 9 | 0,9% | 9 | 1,87% | 9 | 1,9% | 9 | 1,89% |
Willemse (1985) | 9 | 0,9% | 7 | 1,46% | 7 | 1,48% | 0 | 0% |
Brugnera et al. (2020) | 8 | 0,8% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Leavengood et al. (2024) | 8 | 0,8% | 8 | 1,66% | 8 | 1,69% | 8 | 1,68% |
dos Santos et al. (2021) | 7 | 0,7% | 7 | 1,46% | 7 | 1,48% | 7 | 1,47% |
Matile-Ferrero & Williams (2015) | 7 | 0,7% | 7 | 1,46% | 7 | 1,48% | 7 | 1,47% |
Mifsud et al. (2010) | 7 | 0,7% | 7 | 1,46% | 7 | 1,48% | 7 | 1,47% |
Silva et al. (2015) | 7 | 0,7% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Bondar (1923) | 6 | 0,6% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Conjard et al. (2022) | 6 | 0,6% | 6 | 1,25% | 6 | 1,27% | 6 | 1,26% |
Cordeiro & Moreira (2015) | 6 | 0,6% | 6 | 1,25% | 6 | 1,27% | 6 | 1,26% |
Drake (1957) | 6 | 0,6% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Germain (2013) | 6 | 0,6% | 6 | 1,25% | 6 | 1,27% | 6 | 1,26% |
Legros et al. (2017) | 6 | 0,6% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Sanborn (2024) | 6 | 0,6% | 6 | 1,25% | 6 | 1,27% | 6 | 1,26% |
Bonfils et al. (1994) | 5 | 0,5% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Dominique (1892) | 5 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 5 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Hullé & Vernon (2021) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 5 | 0,5% | 4 | 0,83% | 4 | 0,84% | 3 | 0,63% |
Nieser (1969) | 5 | 0,5% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Quilici et al. (1988) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 4 | 0,84% |
Ramage et al. (2023) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Russell & Etienne (1985) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Segarra-carmona et al. (2016) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Streito et al. (2023) | 5 | 0,5% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
Benfatti et al. (2008) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Carvalho (1985) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Costa et al. (2008) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
De Geer (1773) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1902) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Drake (1956) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Etienne & Matile-Ferrero (2008) | 4 | 0,4% | 4 | 0,83% | 2 | 0,42% | 4 | 0,84% |
Fabricius (1794) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1894) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Hullé et al. (2003) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Hullé et al. (2010) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Klyver (1932) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Lupoli & Dusoulier (2015) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Maskell (1893) | 4 | 0,4% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Perez-Gelabert & Floriano (2016) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Pierre (2024) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Poppius (1910) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Schuh & Schwartz (1988) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Touroult et al. (2020) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Touroult et al. (2021) | 4 | 0,4% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
Carvalho & Gomes (1970) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Chartois et al. (2023) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Cohic (1950) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Conjard et al. (2021) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Dadant & Etienne (1973) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Etienne & Champoiseau (2011) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Etienne & Streito (2008) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Kormilev (1971) | 3 | 0,3% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Kozár (2004) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Kreiter et al. (2022) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Laing (1929) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenfant & Marro (1997) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 0 | 0% |
Martinez-Torres et al. (1997) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Mckamey (2010) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Mollot et al. (2016) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Motta et al. (2018) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Panis (1969) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Raspi et al. (2007) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 0 | 0% |
Ribeiro (2005) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Rispe et al. (1999) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Rodrigues et al. (2022) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Román-Palacios et al. (2020) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Segarra-carmona et al. (2020) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Simon et al. (1991) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Slater & Baranowski (1979) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Touroult et al. (2014) | 3 | 0,3% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Touroult et al. (2016) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Touroult et al. (2019) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Touroult et al. (2021) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Vayssières et al. (2017) | 3 | 0,3% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
Albouy et al. (2017) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Bergroth (1914) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Borowiec et al. (2010) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Bout et al. (2021) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Boyer de Fonscolombe (1834) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 0 | 0% |
Brambila (2000) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Castro-huertas et al. (2022) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Cochard et al. (2021) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Cockerell (1893) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Dmitriev (2020) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Duay et al. (2014) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Etienne et al. (1989) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Etienne et al. (1992) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Etienne et al. (2001) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Ezzat (1958) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Fabricius (1781) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1958) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Fennah (1969) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Ferris (1935) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Ferris (1943) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Garrouste & Hervé (2009) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Hartmann et al. (2021) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Hempel (1902) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Hodkinson (1983) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Jourdan et al. (2023) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Knight (1987) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Lopez (1990) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Lotto (1969) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Mamet (1937) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Mamet (1959) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Martin et al. (2001) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Etienne (1996) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Etienne (1998) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Matile-Ferrero & Germain (2004) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Matile-Ferrero et al. (2006) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Matocq & Streito (2022) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Matocq (2022) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Mercado et al. (2016) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Metcalf (1955) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Montrouzier (1861) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Morgan (1889) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Mound et al. (1994) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Nakasuga (1977) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Newstead (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Osborn (1934) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Ouvrard et al. (2016) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Packauskas (2010) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Polhemus (1985) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Polhemus (1997) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Reuter (1875) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribeiro (2007) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Russell (1958) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Russell (1965) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Sanborn (2018) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Slater (1992) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Taquet et al. (2019) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Touroult et al. (2017) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Ueda (2020) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Uhler (1895) | 2 | 0,2% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Usinger & Matsuda (1959) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Votýpka et al. (2020) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Wang et al. (2021) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Yang et al. (2023) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Zheng & Slater (1984) | 2 | 0,2% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
Amyot & Audinet-Serville (1843) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Balachowsky (1958) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Barber (1923) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Beardsley (2000) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Béguinot (2012) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Bianchi et al. (2017) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Bigot (1992) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Boulard (1971) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Brailovsky & Barrera (1994) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Brailovsky & Barrera (2020) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Brailovsky & Perez-Gelabert (2019) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Brailovsky (1990) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Buchanan & White (1879) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Carvalho & Costa (1990) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Cochereau (1966) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Cockerell (1895) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Colligros & Lebecque (2012) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Damgaard & Zettel (2014) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Dedryver et al. (2009) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Della & Giustina (2019) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Dlabola (1963) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Doesburg (1968) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Driss et al. (2024) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Ducos (2023) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Dumbleton (1961) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Dupuis (1999) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Duquef (2016) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Duquef (2017) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Eger Jr et al. (2015) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Elder & Abraham (2012) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etcheberry & Abraham (2009) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etienne et al. (1998) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etienne et al. (1998) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etienne et al. (2014) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etienne et al. (2018) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Etienne (1978) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Eyles (1999) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Fabres (1977) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Fabricius (1787) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1963) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferris (1941) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Garrouste & Cheng (2009) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Garrouste (2015) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Germain & Chapin (2004) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Germain & Streito (2004) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Germain et al. (2007) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 0 | 0% |
Germain et al. (2014) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Germar (1821) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Goux (1937) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 0 | 0% |
Green (1896) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hall (1946) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Hammes & Putoa (1986) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Haupt (1927) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Heckman (2011) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Heidemann (1908) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Heiss & Moragues (2009) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Heiss (2011) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hempel (1901) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hempel (1922) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Herring (1961) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Hodges & Hodgson (2010) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Horváth (1909) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hulle et al. (1996) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Jansson (1982) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Jensen-haarup (1926) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2022) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Jurberg et al. (2015) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Kormilev (1965) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kozar & Benedicty (2003) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Languillon (1951) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Leonard (1968) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Linnaeus (1761) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Lucas (1872) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli (2019) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2008) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Mary (2017) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Mckenzie (1937) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Mouttet & Balmès (2021) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Newstead (1909) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas et al. (2024) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Nieser (1970) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Onillon et al. (1995) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Osborn (1926) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ouvrard et al. (2015) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Palisot & Beauvois (1820) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez-gelabert & Thomas (2005) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Piron (2010) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Quilici et al. (1998) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Ramage (2024) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Razafindrakoto & Matile-ferrero (2013) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Rider & Chapin (1992) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Rosa et al. (2016) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Sanborn (2011) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Sauvion et al. (1999) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Schuh & Schwartz (1985) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Spangler et al. (1985) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Streito & Étienne (2020) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Streito & Morival (2005) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Streito (2004) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Swanson (2018) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 0 | 0% |
Takahashi (1955) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Touroult et al. (2022) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Touroult et al. (2024) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Unruh & Gullan (2008) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
van Doesburg (1968) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Duzee (1937) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Williams (1961) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Wygodzinsky & Schmidt (1991) | 1 | 0,1% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
Zilli (2021) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |