Espèces (sub)endémiques dans la dernière version et qui ne le sont plus
446 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fournet (2002) | 194 | 22,69% | 146 | 45,62% | 146 | 48,5% | 146 | 48,5% |
Molino et al. (2022) | 142 | 16,61% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Funk et al. (2007) | 60 | 7,02% | 15 | 4,69% | 15 | 4,98% | 15 | 4,98% |
Acevedo-Rodríguez & Strong (2012) | 53 | 6,2% | 49 | 15,31% | 49 | 16,28% | 49 | 16,28% |
Véron et al. (2021) | 33 | 3,86% | 32 | 10% | 32 | 10,63% | 32 | 10,63% |
Meurgey & Ramage (2020) | 23 | 2,69% | 23 | 7,19% | 22 | 7,31% | 22 | 7,31% |
Tison et al. (2014) | 22 | 2,57% | 14 | 4,38% | 12 | 3,99% | 13 | 4,32% |
Meurgey (2011) | 21 | 2,46% | 17 | 5,31% | 17 | 5,65% | 16 | 5,32% |
Munzinger et al. (2016) | 20 | 2,34% | 5 | 1,56% | 4 | 1,33% | 5 | 1,66% |
Peck et al. (2014) | 19 | 2,22% | 17 | 5,31% | 17 | 5,65% | 16 | 5,32% |
Kieffer & Marshall (1904) | 18 | 2,11% | 15 | 4,69% | 15 | 4,98% | 15 | 4,98% |
Marhic (2022) | 16 | 1,87% | 16 | 5% | 16 | 5,32% | 16 | 5,32% |
Kieffer (1907-1911) | 15 | 1,75% | 8 | 2,5% | 8 | 2,66% | 8 | 2,66% |
Morat et al. (2012) | 13 | 1,52% | 7 | 2,19% | 6 | 1,99% | 6 | 1,99% |
Talaga et al. (2015) | 13 | 1,52% | 13 | 4,06% | 13 | 4,32% | 13 | 4,32% |
Eggers (1940) | 12 | 1,4% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Gallard & Wood (2017) | 12 | 1,4% | 11 | 3,44% | 2 | 0,66% | 11 | 3,65% |
Yeates (1992) | 12 | 1,4% | 12 | 3,75% | 12 | 3,99% | 12 | 3,99% |
Bright (2019) | 11 | 1,29% | 10 | 3,12% | 10 | 3,32% | 10 | 3,32% |
Peck (2011) | 11 | 1,29% | 11 | 3,44% | 11 | 3,65% | 11 | 3,65% |
Chalumeau & Touroult (2005) | 10 | 1,17% | 10 | 3,12% | 10 | 3,32% | 10 | 3,32% |
Kieffer (1914) | 10 | 1,17% | 8 | 2,5% | 8 | 2,66% | 8 | 2,66% |
Lescure et al. (2012) | 10 | 1,17% | 7 | 2,19% | 7 | 2,33% | 7 | 2,33% |
Peck (2011) | 10 | 1,17% | 10 | 3,12% | 9 | 2,99% | 7 | 2,33% |
Ramage (2017) | 10 | 1,17% | 9 | 2,81% | 9 | 2,99% | 9 | 2,99% |
Ter Steege et al. (2016) | 9 | 1,05% | 9 | 2,81% | 9 | 2,99% | 9 | 2,99% |
Arnold & Ovenden (2014) | 8 | 0,94% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Dupuis & Perrin (2020) | 8 | 0,94% | 8 | 2,5% | 7 | 2,33% | 7 | 2,33% |
Ferrufino-acosta (2010) | 8 | 0,94% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Kieffer (1906) | 8 | 0,94% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Massary et al. (2019) | 7 | 0,82% | 7 | 2,19% | 7 | 2,33% | 7 | 2,33% |
Bour et al. (2008) | 6 | 0,7% | 5 | 1,56% | 5 | 1,66% | 5 | 1,66% |
Brévignon & Gallard (1997) | 6 | 0,7% | 6 | 1,88% | 3 | 1% | 6 | 1,99% |
Clastrier (1970) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Evenhuis (2018) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Graham (1991) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Grand et al. (2014) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Grand et al. (2019) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Hielkema & Hielkema (2019) | 6 | 0,7% | 6 | 1,88% | 5 | 1,66% | 6 | 1,99% |
Molino et al. (2009) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 6 | 1,99% |
Noblecourt (2016) | 6 | 0,7% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Ponchel (2011) | 6 | 0,7% | 6 | 1,88% | 6 | 1,99% | 5 | 1,66% |
Abeille & Perrin (1878) | 5 | 0,58% | 3 | 0,94% | 2 | 0,66% | 1 | 0,33% |
Degallier (2012) | 5 | 0,58% | 5 | 1,56% | 5 | 1,66% | 5 | 1,66% |
Emery (1914) | 5 | 0,58% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Hermans & Cribb (2021) | 5 | 0,58% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Johnson et al. (2021) | 5 | 0,58% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Martiré & Rochat (2008) | 5 | 0,58% | 5 | 1,56% | 5 | 1,66% | 5 | 1,66% |
Pillon & Hequet (2019) | 5 | 0,58% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Rouhan et al. (2008) | 5 | 0,58% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Thomson (2023) | 5 | 0,58% | 5 | 1,56% | 5 | 1,66% | 5 | 1,66% |
Ah-Peng et al. (2010) | 4 | 0,47% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Bayer et al. (2020) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Botosaneanu (2002) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Christenhusz (2009) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Duguet & Melki (2003) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Graham (1984) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Guillermet (2009) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Hewitson (1867-1871) | 4 | 0,47% | 2 | 0,62% | 2 | 0,66% | 0 | 0% |
Holovachov (2019) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Jourdan (2020) | 4 | 0,47% | 4 | 1,25% | 3 | 1% | 3 | 1% |
Kwet (2009) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Latreille (1805) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Miaud & Muratet (2018) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Moore et al. (2018) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Niogret et al. (2007) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Pailler & Henze (2020) | 4 | 0,47% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Ponchel (2015) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Senevet & Abonnenc (1939) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Serre-collet (2013) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Thirion & Evrard (2012) | 4 | 0,47% | 4 | 1,25% | 4 | 1,33% | 4 | 1,33% |
Aubert (1979) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Beeson (1935) | 3 | 0,35% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bernard (2015) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Bippus (2018) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Bonfils et al. (2001) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Botosaneanu (1988) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Buysson (1887) | 3 | 0,35% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Caporiacco (1954) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Chevin (1986) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Delvare (1986) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Duval et al. (1978) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Fain & Gaud (1972) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Fauvel (1903) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Feldmann (2012) | 3 | 0,35% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Fritsch (2003) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Gallard (2014) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Grolle (1995) | 3 | 0,35% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hustache (1932) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Huttel & Huttel (1954) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Jennings et al. (2013) | 3 | 0,35% | 3 | 0,94% | 2 | 0,66% | 3 | 1% |
Lardeux & Ottenwaelder (1997) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Lehnert (2012) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Lieftinck (1975) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Mary (2017) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Mertens (1957) | 3 | 0,35% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Nicolas (1977) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Niedbała (1998) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Questel & Le Quellec (2012) | 3 | 0,35% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Questel (2020) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 2 | 0,66% |
Ris (1915) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Stephensen (1935) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Suessenguth (1936) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Taylor (1987) | 3 | 0,35% | 2 | 0,62% | 1 | 0,33% | 2 | 0,66% |
Vaillant (1988) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Vedel et al. (2013) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Wheeler (1935) | 3 | 0,35% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Wigginton (2009) | 3 | 0,35% | 3 | 0,94% | 3 | 1% | 3 | 1% |
Abeille de Perrin (1877) | 2 | 0,23% | 2 | 0,62% | 1 | 0,33% | 1 | 0,33% |
Ah-Peng & Bardat (2011) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Anker (2010) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Anonyme (2014) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Aubert (1969) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubert (1971) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Azevedo et al. (2018) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Barjadze et al. (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Berland & Bernard (1938) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Bernard (1935) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Bigot (1887) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bippus (2019) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Bippus (2020) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Boggan et al. (1992) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Borchsenius & Bernal (1996) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Borkent & Dominiak (2020) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Botosaneanu (1994) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Boyer & Fonscolombe (1840) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Caballer & Ortea (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Cardoso & Braga (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Chovet et al. (2023) | 2 | 0,23% | 2 | 0,62% | 0 | 0% | 2 | 0,66% |
Clastrier (1970) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Coiffait (1976) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Colijn et al. (2020) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 1 | 0,33% |
Cooreman (1959) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1777]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Daly (1992) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
de Massary et al. (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Dechambre (1997) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Degallier & Gomy (2024) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Dégallier et al. (2017) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Della & Giustina (2019) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Diakonoff (1978) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Dierkens (2013) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Dominiak & Szadziewski (2010) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Eaton (1875) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Fauran (1955) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Fleutiaux & Sallé ([1890]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1997) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Gasper et al. (2016) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gaulle (de) (1907) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gnezdilov & Bartlett (2022) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Goldenberg et al. (2013) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
González-Gutiérrez (2007) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Gradstein & Ilkiu-borges (2021) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Gradstein & Lavocat Bernard (2020) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Graham (1987) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Grolle & Long (2000) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (1992) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Guillermet (2009) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Guillermet (2011) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Guillermet (2011) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Hart & Ivie (2016) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Heller (1916) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Hewitson (1871) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 0 | 0% |
Hugonnot & Hedenäs (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Hullé et al. (2018) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Hustache (1920) | 2 | 0,23% | 2 | 0,62% | 0 | 0% | 2 | 0,66% |
Hynes (1993) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Kieffer (1902) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Kieffer (1908) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Kimmins (1936) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Kowalkowska & Margonska (2012) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Lacourt (1988) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Lacourt (1998) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Leseigneur & Dalmon (2006) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Linsenmaier (1959) | 2 | 0,23% | 1 | 0,31% | 0 | 0% | 1 | 0,33% |
Liston et al. (2019) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Lupoli & Dusoulier (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Manuel (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Margońska (2019) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Marline (2018) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Matile (1988) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Migeon (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Mille (2008) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Moczar (1997) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Monné & Napp (2000) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Morat & Veillon (1985) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Muratet (2015) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Niedbała & Penttinen (2007) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Oustalet (1895) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Pace (1987) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Perroud & Montrouzier (1864) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Picard (1919) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Probst (1997) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Rainer (2002) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Reeb & Gradstein (2020) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Rheinheimer (2023) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Rosa (2024) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 0 | 0% |
Seifert & Galkowski (2016) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Seifert (2020) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Senevet & Abonnenc (1938) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Senevet & Abonnenc (1939) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Senevet et al. (1942) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Shoemaker (1942) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Soldati & Touroult (2014) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Taczanowski (1871) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Thumsová et al. (2022) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 1 | 0,33% |
Uicn et al. (2012) | 2 | 0,23% | 2 | 0,62% | 2 | 0,66% | 2 | 0,66% |
Yokoyama (2013) | 2 | 0,23% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Abeille de Perrin (1877) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Abeille de Perrin (1879) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Allemand & Thilliez (1991) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Anker (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Anonyme. (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Anonyme (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Aubert (1960) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Aublet (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker & Pritchard (1960) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Barabé & Gibernau (2015) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bauer (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bedriaga (1883) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bedriaga (1889) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellone & Chiron (2003) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Berland (1928) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard & Etifier-Chalono (2006) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Beron (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Berroneau (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Berthoumieu (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Betta (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Blackwelder (1943) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Blair (1934) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Boggan et al. (1997) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Böining et al. (2024) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bombi & Vignoli (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bos et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bosmans (1997) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Boulenger (1891) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Boullet et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Bouyon (1995) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Boyd et al. (2006) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Breuil (2009) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Brévignon & Gallard (1993) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Brévignon & Gallard (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Brochier (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Brown (2009) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Camerano (1885) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Carranza & Arribas (2008) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Cavro (1950) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cazanove (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Chalumeau (1983) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Chambers & Wilson (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Clarke & Lanza (1990) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Clavier et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Clavier et al. (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Coiffait (1977) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Comstock (1943) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Constantin (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Copeland (1932) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Corporaal (1937) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Corti et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Coste & Soulié (1905) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Couhia & Fleurot (2016) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Courtial (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Cremers & Boudrie (2006) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Cremers & Boudrie (2007) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Cremers & Hoff (1992) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Daly & Fine (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dechambre & Duranton (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dechambre (1992) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Degallier et al. (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Degallier et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Degallier (1981) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Déjean et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Deliry (1996) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Meyer (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Denis (1933) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Denis (1934) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dewynter et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dewynter et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Dewynter et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Do Vale et al. (2017) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dominique (1892) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1993) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Drillon et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Duchaussoy (1916) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ducke (1904) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ducke (1910) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguet et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Annales de la société entomologique de France, 22(2): 205-210.">Dupuis (1986) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Duyck et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Dyar (1920) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ebihara et al. (2006) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ellis et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ellis et al. (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Evenhuis (1989) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Evenhuis (1991) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Evenhuis (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fabricius (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Farhad et al. (2015) | 1 | 0,12% | 1 | 0,31% | 0 | 0% | 1 | 0,33% |
Fauvel (1867) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fauvel (1877) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fennah (1958) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ferlay et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ferragu (1979) | 1 | 0,12% | 1 | 0,31% | 0 | 0% | 1 | 0,33% |
Feuillet (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fine et al. (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fisher & Fong (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Fleuriau & Bosc (2015) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Florence (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Fournier (1934-1940) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (1988) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Furth (1998) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gallard (2013) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gasca-Alvarez et al. (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gnezdilov (2009) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gokhman (2007) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Gomy (2000) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Gosá et al. (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Guilbert & Casevitz-Weulersse (1997) | 1 | 0,12% | 1 | 0,31% | 0 | 0% | 1 | 0,33% |
Gutierrez & Etienne (1986) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hammer (1972) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hammer (1972) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hancock (2008) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hodgetts & Lockhart (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Howard (1988) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Hullé & Vernon (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Johansson (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Kalkman & Theischinger (2013) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Keymar (1988) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Kieffer (1910) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Konvička & Brustel (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Kramer (1957) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Lamarck (1779) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamas (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Lamy & Pointier (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Lanza et al. (1986) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Laubengayer et al. (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Lauriaut et al. (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Lazell (1994) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebard & Claude (2024) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Lebas & Galkowski (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ledoux (2004) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1955) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Levesque & Delcroix (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Libro et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Linnaeus (1753) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Linnaeus (1758) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linsenmaier (1987) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Llamas et al. (1998) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Maas et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Macquart (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Malicky (1983) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Maneval (1930) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Maneval (1935) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Marshall (1874) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Mertens & Wermuth (1960) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mickel (1997) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Mille et al. (2016) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Móczár (1970) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Moench (1794) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod & Dollfus (1932) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Moonlight et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Mori et al. (2002) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Nascetti et al. (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicola & Ferer (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Niedbała & Liu (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Norrbom & Hancock (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Orhant (2003) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ortea et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Otth (1837) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Pabijan et al. (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Pace (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Pailler et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Paulian (1998) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Pease (1869) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Perrault (1979) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Peters (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pires et al. (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Poupin (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Ratcliffe & Cave (2015) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Remillet (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Renet et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Reverté et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Richard (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Richards (1939) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Riedel (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Rosa & Vas (2017) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Rouy (1909) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruiz & Brescovit (2008) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Saïd et al. (2017) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Salisbury (1796) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvidio et al. (1997) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Schäfer-Verwimp & Van Melick (2016) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Schmid-Egger (2011) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Schneider & Zizka (2016) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Schneider & Zizka (2017) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Senevet (1937) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra-cobo (1993) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Shaw et al. (2016) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Somavilla et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Soto Arenas & Cribb (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Speight (2013) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Stehlé & Stehlé (1958) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Stöck et al. (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Strachinis et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Surget-Groba & Thorpe (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Szita et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Talaga & Duchemin (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Talaga et al. (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Talebi et al. (2011) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Tavakilian & Chevillotte (2013) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Touroult et al. (2022) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Touroult (2004) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Touroult (2012) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Triapitsyn (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Trochet et al. (2024) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Tronquet (2014) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Turner (1919) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Tussac & Tussac (2005) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Uicn et al. (2015) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Uicn et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Vachal (1907) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Van der Smissen (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 0 | 0% |
Vas et al. (2024) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Veith (1996) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Vieira et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Villiers (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Villiers (1980) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1846) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Weinell et al. (2019) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Westwood (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiegmann (1834) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Yefremova & Strakhova (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Yvinec (2010) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Yvinec (2021) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Zakardjian et al. (2020) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Zakardjian et al. (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Zangari et al. (2006) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Zeegers & Pollet (2023) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |
Zikic et al. (2018) | 1 | 0,12% | 1 | 0,31% | 1 | 0,33% | 1 | 0,33% |