Diptères de Guadeloupe
Diptera de Guadeloupe
221 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) | 302 | 44,41% | 300 | 94,34% | 300 | 94,34% | 300 | 94,34% |
Meurgey (2011) | 144 | 21,18% | 120 | 37,74% | 120 | 37,74% | 120 | 37,74% |
Martinez & Etienne (2002) | 90 | 13,24% | 90 | 28,3% | 90 | 28,3% | 90 | 28,3% |
Spencer et al. (1992) | 74 | 10,88% | 73 | 22,96% | 73 | 22,96% | 73 | 22,96% |
Etienne & Martinez (2013) | 49 | 7,21% | 49 | 15,41% | 49 | 15,41% | 49 | 15,41% |
Etienne & Martinez (2003) | 48 | 7,06% | 48 | 15,09% | 48 | 15,09% | 48 | 15,09% |
Etienne & Gagné (2017) | 47 | 6,91% | 47 | 14,78% | 47 | 14,78% | 47 | 14,78% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 38 | 5,59% | 36 | 11,32% | 36 | 11,32% | 36 | 11,32% |
Grogan et al. (2016) | 36 | 5,29% | 36 | 11,32% | 36 | 11,32% | 36 | 11,32% |
Grogan et al. (2013) | 27 | 3,97% | 25 | 7,86% | 25 | 7,86% | 25 | 7,86% |
Matile (1982) | 26 | 3,82% | 26 | 8,18% | 26 | 8,18% | 26 | 8,18% |
Etienne & Martinez (1996) | 25 | 3,68% | 23 | 7,23% | 23 | 7,23% | 23 | 7,23% |
Questel (2020) | 16 | 2,35% | 13 | 4,09% | 13 | 4,09% | 13 | 4,09% |
Talaga et al. (2015) | 16 | 2,35% | 16 | 5,03% | 16 | 5,03% | 16 | 5,03% |
Ramage (2017) | 15 | 2,21% | 15 | 4,72% | 15 | 4,72% | 15 | 4,72% |
Borges & Couri (2009) | 13 | 1,91% | 5 | 1,57% | 5 | 1,57% | 5 | 1,57% |
Jourdan & Mille (2006) | 11 | 1,62% | 10 | 3,14% | 10 | 3,14% | 10 | 3,14% |
Delécolle & Rieb (1994) | 9 | 1,32% | 6 | 1,89% | 6 | 1,89% | 6 | 1,89% |
Evenhuis (2018) | 9 | 1,32% | 9 | 2,83% | 9 | 2,83% | 9 | 2,83% |
Thompson (1981) | 9 | 1,32% | 8 | 2,52% | 8 | 2,52% | 8 | 2,52% |
Martinez & Étienne (2002) | 8 | 1,18% | 8 | 2,52% | 8 | 2,52% | 8 | 2,52% |
Paulian (1998) | 8 | 1,18% | 8 | 2,52% | 8 | 2,52% | 8 | 2,52% |
Gagné & Etienne (2009) | 6 | 0,88% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Gagné & Etienne (2015) | 6 | 0,88% | 6 | 1,89% | 6 | 1,89% | 6 | 1,89% |
Pierre et al. (2017) | 6 | 0,88% | 5 | 1,57% | 5 | 1,57% | 5 | 1,57% |
Spencer (1963) | 6 | 0,88% | 5 | 1,57% | 5 | 1,57% | 5 | 1,57% |
Touroult et al. (2023) | 6 | 0,88% | 6 | 1,89% | 6 | 1,89% | 6 | 1,89% |
Wulp (1882) | 6 | 0,88% | 0 | 0% | 0 | 0% | 0 | 0% |
Bickel (2003) | 5 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominiak (2012) | 5 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 5 | 0,74% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Malloch (1913) | 5 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
Remillet (1988) | 5 | 0,74% | 5 | 1,57% | 5 | 1,57% | 5 | 1,57% |
Theobald (1901) | 5 | 0,74% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Dumbardon-Martial & Delblond (2019) | 4 | 0,59% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Dumbardon-martial et al. (2023) | 4 | 0,59% | 4 | 1,26% | 4 | 1,26% | 4 | 1,26% |
Felt (1907) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Floch & Abonnenc (1952) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Fox (1946) | 4 | 0,59% | 4 | 1,26% | 4 | 1,26% | 4 | 1,26% |
Gagné et al. (2000) | 4 | 0,59% | 4 | 1,26% | 4 | 1,26% | 4 | 1,26% |
Pierre & Dumbardon-Martial (2016) | 4 | 0,59% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Rageau (1958) | 4 | 0,59% | 4 | 1,26% | 4 | 1,26% | 4 | 1,26% |
Ramage et al. (2018) | 4 | 0,59% | 4 | 1,26% | 4 | 1,26% | 4 | 1,26% |
Senevet & Abonnenc (1939) | 4 | 0,59% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Sénévet (1938) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Williston (1896) | 4 | 0,59% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Williston (1896) | 4 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2018) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
David & Tsacas (1975) | 3 | 0,44% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
David et al. (2014) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Dumbardon-martial (2015) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Evenhuis (2007) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Fabricius (1775) | 3 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Gagné & Etienne (2006) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Gagné & Etienne (2019) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Gutierrez (1981) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Le Maitre & Chadee (1983) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Neveu-Lemaire (1902) | 3 | 0,44% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
O’Hara et al. (2020) | 3 | 0,44% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Questel & Le Quellec (2012) | 3 | 0,44% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Rageau (1956) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Robineau-desvoidy (1827) | 3 | 0,44% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Senevet (1937) | 3 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Spencer & Stegmaier (1973) | 3 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga & Duchemin (2023) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Touroult et al. (2016) | 3 | 0,44% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Touroult et al. (2018) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Touroult et al. (2021) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Waller et al. (1990) | 3 | 0,44% | 3 | 0,94% | 3 | 0,94% | 3 | 0,94% |
Amouroux et al. (2013) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Bangy et al. (2009) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Bickel (1994) | 2 | 0,29% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Borkent (2008) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Bousses et al. (2013) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Coquillett (1906) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Aguilar & Martinez (1979) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Dusfour et al. (2013) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Dyar & Knab (1906) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Etienne et al. (2018) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Evenhuis (2007) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Evenhuis (2011) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Evenhuis (2012) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Fabricius (1794) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Felt (1911) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Frick (1952) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Frost (1931) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Frost (1936) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1953) | 2 | 0,29% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Hery et al. (2020) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Jourdan (2020) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Kurahashi & Fauran (1980) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Labat (2023) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Malloch (1914) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1933) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Marie & Bossin (2013) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Martinez (1994) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Meganck et al. (2017) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Mengual et al. (2009) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Metz & Webb (2003) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Nibouche et al. (202X) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Rageau (1959) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Ramage et al. (2017) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Rioux et al. (1985) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Robinson (1975) | 2 | 0,29% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Senevet (1936) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Shinonaga et al. (1991) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Spencer (1973) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Spencer (1988) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Spinelli et al. (2015) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Touroult et al. (2015) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Touroult et al. (2020) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Tsacas & Chassagnard (1988) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Vayssières et al. (2001) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Whitworth (2014) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Wiedemann ([1820]-1821) | 2 | 0,29% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Wulp (1883) | 2 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Yassin et al. (2012) | 2 | 0,29% | 2 | 0,63% | 2 | 0,63% | 2 | 0,63% |
Adler (2020) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Albouy et al. (2017) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Aldrich (1929) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagny et al. (2009) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Belkin et al. (1965) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (1890) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchard (1926) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkent & Wirth (1997) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Broadhead (1989) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Brunhes & Boussès (2009) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Brunhes (1977) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Brunhes (1979) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Chevin (1986) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Chown & Convey (2016) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Clastrier & Legrand (1990) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Coquillett (1905) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Cresson (1926) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Curran (1929) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Curry (1932) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (2003) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Diniz & Freitas (1986) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Duda (1940) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (2018) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dumbardon-Martial & Marshall (2015) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dumbardon-martial (2017) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dyar & Knab (1906) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dyar & Knab (1906) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Dyar & Knab (1906) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Dyar & Knab (1907) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Dyar (1920) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Edwards (1931) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Edwards (1933) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Etienne et al. (2004) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Etienne (1971) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Evans (1924) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2011) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Evenhuis (2012) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Evenhuis (2012) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Evenhuis (2013) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Fabricius (1781) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Felt (1911) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Felt (1927) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Frick (1956) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Frost (1924) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gagné & Jaschhof (2014) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Gagne (2004) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Gaimari & Silva (2020) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Germain et al. (2014) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Gordon & Evans (1922) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamada & Fouque (2001) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Harris (1968) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hendel (1923) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hering (1951) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Hull (1937) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Irish et al. (2014) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Kassebeer (2000) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Knab (1913) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lagarde (2008) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Lane (1950) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebard & Hauser (2023) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Liénard et al. (2011) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Macfie (1937) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Macfie (1940) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Madi-Ravazzi et al. (2021) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Malloch (1914) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Malloch (1932) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Maquart et al. (2020) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Marcos-garcía et al. (2013) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Marks (1951) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Mcevey & Schiffer (2015) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Mederos et al. (2023) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Melander (1913) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Mengual et al. (2008) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Mille et al., 2012 | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Pollet et al. (2004) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Rozkosny (1983) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Sasakawa (1963) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Sasakawa (1963) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Say (1823) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Skuhrava et al. (2005) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Steyskal (1975) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Steyskal (1980) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Szadziewski & Dominiak (2006) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Talaga et al. (2021) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Theobald (1913) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Tomasovic (2002) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Touroult et al. (2019) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Touroult et al. (2021) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Townsend (1915) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Townsend (1927) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Duzee (1927) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2013) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Vieira et al. (2019) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Walker (1848) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiedemann (1819) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiedemann (1828) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiedemann (1830) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Wirth & Blanton (1956) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
Wolff et al. (2016) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,15% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |