Espèces à PNA
817 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Tison et al. (2014) | 220 | 10,41% | 113 | 46,12% | 110 | 45,64% | 109 | 45,23% |
Cambecèdes et al. (2012) | 83 | 3,93% | 82 | 33,47% | 80 | 33,2% | 81 | 33,61% |
Aulagnier (2009) | 44 | 2,08% | 44 | 17,96% | 44 | 18,26% | 44 | 18,26% |
Aulagnier et al. (2017) | 42 | 1,99% | 40 | 16,33% | 40 | 16,6% | 40 | 16,6% |
Mertens & Wermuth (1960) | 42 | 1,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafranchis (2014) | 38 | 1,8% | 29 | 11,84% | 29 | 12,03% | 29 | 12,03% |
Lafranchis (2016) | 38 | 1,8% | 29 | 11,84% | 29 | 12,03% | 29 | 12,03% |
Linnaeus (1758) | 35 | 1,66% | 8 | 3,27% | 8 | 3,32% | 7 | 2,9% |
Arthur & Lemaire (2015) | 34 | 1,61% | 34 | 13,88% | 34 | 14,11% | 34 | 14,11% |
Dietz & Kiefer (2015) | 34 | 1,61% | 34 | 13,88% | 34 | 14,11% | 34 | 14,11% |
Houard & Jaulin (2018) | 34 | 1,61% | 34 | 13,88% | 34 | 14,11% | 34 | 14,11% |
Godineau & Pain (2007) | 33 | 1,56% | 33 | 13,47% | 33 | 13,69% | 33 | 13,69% |
Houard (2020) | 33 | 1,56% | 33 | 13,47% | 33 | 13,69% | 33 | 13,69% |
Grand et al. (2014) | 32 | 1,51% | 31 | 12,65% | 31 | 12,86% | 31 | 12,86% |
Grand & Boudot (2007) | 31 | 1,47% | 30 | 12,24% | 30 | 12,45% | 30 | 12,45% |
Dijkstra et al. (2015) | 30 | 1,42% | 29 | 11,84% | 29 | 12,03% | 29 | 12,03% |
Heidemann & Seidenbusch (2002) | 29 | 1,37% | 28 | 11,43% | 28 | 11,62% | 28 | 11,62% |
Doucet (2016) | 24 | 1,14% | 23 | 9,39% | 23 | 9,54% | 23 | 9,54% |
Arnold & Ovenden (2014) | 19 | 0,9% | 13 | 5,31% | 13 | 5,39% | 13 | 5,39% |
Tapiero et al. (2017) | 19 | 0,9% | 19 | 7,76% | 19 | 7,88% | 19 | 7,88% |
Dupont (2010) | 18 | 0,85% | 16 | 6,53% | 16 | 6,64% | 16 | 6,64% |
Lescure et al. (2012) | 17 | 0,8% | 14 | 5,71% | 14 | 5,81% | 14 | 5,81% |
Massary et al. (2019) | 15 | 0,71% | 15 | 6,12% | 15 | 6,22% | 15 | 6,22% |
Uicn et al. (2015) | 15 | 0,71% | 15 | 6,12% | 15 | 6,22% | 15 | 6,22% |
Van Dijk et al. (2012) | 15 | 0,71% | 12 | 4,9% | 12 | 4,98% | 12 | 4,98% |
Bour et al. (2008) | 14 | 0,66% | 14 | 5,71% | 14 | 5,81% | 14 | 5,81% |
Linnaeus (1753) | 14 | 0,66% | 10 | 4,08% | 10 | 4,15% | 10 | 4,15% |
Rouy & Foucaud (1893) | 11 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril (1870) | 10 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratet (2015) | 10 | 0,47% | 9 | 3,67% | 9 | 3,73% | 9 | 3,73% |
de Massary et al. (2015) | 8 | 0,38% | 8 | 3,27% | 8 | 3,32% | 8 | 3,32% |
Esper & Charpentier (1789-[1804]) | 8 | 0,38% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Jordan (1861) | 8 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Wahlsteen & Tyler (2019) | 8 | 0,38% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
[Denis & Schiffermüller] (1775) | 7 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Esper (1780-1786) | 7 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1890) | 7 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2012) | 7 | 0,33% | 7 | 2,86% | 7 | 2,9% | 7 | 2,9% |
Oberthür (1910) | 7 | 0,33% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Camiñas et al. (2021) | 6 | 0,28% | 6 | 2,45% | 6 | 2,49% | 6 | 2,49% |
Ugelvig et al. (2011) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2017) | 6 | 0,28% | 6 | 2,45% | 6 | 2,49% | 6 | 2,49% |
Bioinsight/diren & Guyane (2006) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Casale et al. (2021) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Chevalier (2006) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Ciccione et al. (2011) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Crillon & Cuzange (2020) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dewynter et al. (2019) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dewynter et al. (2019) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dewynter et al. (2022) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dewynter et al. (2023) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dewynter et al. (2023) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Duffaut et al. (2011) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Dupont (2010) | 5 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Entraygues (2014) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Étaix-bonnin et al. (2011) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Falkner et al. (2002) | 5 | 0,24% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Fretey & Triplet (2022) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Heppner (1981) | 5 | 0,24% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Le Scao et al. (2011) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Massary et al. (2018) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Massary et al. (2020) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Massary et al. (2021) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Probst et al. (2022) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Questel et al. (2023) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Questel et al. (2023) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Read & Farman (2018) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Read et al. (2023) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Rhodin et al. (2017) | 5 | 0,24% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Sauvignet et al. (2000) | 5 | 0,24% | 5 | 2,04% | 5 | 2,07% | 5 | 2,07% |
Arcangeli (1882) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubouin et al. (2016) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Barrioz & Morinière (2007) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Bonnier (1912) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Booister (2009) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Dujardin (1956) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Escoriza et al. (2023) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Esper & Charpentier (1789-[1804]) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournet (2002) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Fretey & Lescure (1999) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Gargominy et al. (2011) | 4 | 0,19% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Göktürk & Sümbül (2014) | 4 | 0,19% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lefranc & Issa (2013) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Massary et al. (2017) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Nyman (1882) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié (2017) | 4 | 0,19% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Probst (1997) | 4 | 0,19% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Probst (2001) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Questel & Le Quellec (2012) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Questel (2020) | 4 | 0,19% | 4 | 1,63% | 4 | 1,66% | 4 | 1,66% |
Rambur (1837-1840) | 4 | 0,19% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rambur (1858-[1866]) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Rottemburg (1775) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Salisbury (1796) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema et al. (2018) | 4 | 0,19% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Bauer & Sadlier (2000) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Bell (1982) | 3 | 0,14% | 3 | 1,22% | 2 | 0,83% | 3 | 1,24% |
Blanc (1909) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bussiere & Labrousse (2015) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Csutoros (2024) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Delcroix et al. (2011) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Dubief & Gallais (2011) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Duguy et al. (1998) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Duguy et al. (2007) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Duguy (1988) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Duguy (1994) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Duguy (1997) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Dulac (1867) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Euro+Med (2006) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fric et al. (2007) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot (2011) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Hequet & Le Corre (2010) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Hequet et al. (2009) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Herbrecht & Dommanget (2006) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Hoff & Daszkiewicz (2001) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Honey & Scoble (2001) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (2017) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Jacquet (2009) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Linnaeus (1753) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1764) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopes-Lima et al. (2016) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
MacKee (1994) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Méheust et al. (2018) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Moneglia et al. (2009) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Morinière & Dell'amico (2011) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Poisson (1999) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Pottier (2012) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Probst (1998) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Read & Jean (2021) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Ronot (2007) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Sharpe (1894) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Uicn et al. (2012) | 3 | 0,14% | 3 | 1,22% | 3 | 1,24% | 3 | 1,24% |
Verity (1947) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez & Strong (2012) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Arribas (1993) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Arroyo et al. (2020) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Aulagnier (2021) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Bachelard & Fournier (2010) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baldi et al. (2022) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Bergsträsser (1779) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Billi et al. (2011) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Blanchet et al. (1998) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Boudarel & Scher (2022) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Boyer De Fonscolombe (1838) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Burger et al. (2013) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Butler (1868) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1821) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cazals & Dupont (2022) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Chaix (1785) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Champagne et al. (1997) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Charpentier (1825) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheke (1987) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Chevallier et al. (2023) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Courant & Meme-Lafond (2011) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Cramer ([1775-1776]) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Cyrillo (1787) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Denis et al. (2020) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Dierks (2006) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguet & Melki (2003) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (1997) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (1999) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (2000) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (2002) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (2003) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (2004) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy et al. (2006) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1987) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1990) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1992) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1993) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1995) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Duguy (1996) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Etcheberry & Abraham (2009) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Fabricius ([1777]) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiori (1925) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1868) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Freitag & Iamonico (2015) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2001) | 2 | 0,09% | 2 | 0,82% | 1 | 0,41% | 2 | 0,83% |
Geoffroy (1762) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard-claudon & Ribatto (2016) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Girondo (2023) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Gray (1821) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Godron (1848) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Grum-Grshimailo (1893) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Higgins (1978) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hirschke (1904-1905) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner ([1799-1800]) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Illiger (1803) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Isenmann et al. (2000) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Jouan (1863) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Joubert & Margerit (1986) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Karadjian et al. (2022) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Keyserling & Blasius (1839) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kwet (2009) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Lajonquière (1965) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamand & Prié (2017) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lambert (1988) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambret (2013) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Leraut (1997) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1762) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lustrat (1987) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Maran & Frétey (2023) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Mazel (1979) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrem (1820) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Mertens (1957) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Miaud & Muratet (2018) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Momont (1998) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Naveira et al. (2023) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Nazari et al. (2009) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Parise et al. (2012) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Paul & Lefranc (2011) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Peron (2014) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Pictet (1843) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2000) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Probst et al. (2001) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Revaka et al. (2012) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rinaldi et al. (2011) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Rochelet (2008) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Roux (1913) | 2 | 0,09% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rouy (1913) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Sagarra (1930) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1906) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 1 | 0,41% |
Schreber (1774) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Serre-collet (2013) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Staudinger & Wocke (1861) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Stichel (1908) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Thirion & Evrard (2012) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Thunberg (1787) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Tirvengadum & Bour (1985) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Vaillant (2000) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Van Dijk et al. (2014) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1920) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1925) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1927) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1947-1951) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Villard et al. (2013) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Wolff et al. (2012) | 2 | 0,09% | 2 | 0,82% | 2 | 0,83% | 2 | 0,83% |
Zetterstedt ([1838]-1840) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Abhaya & Probst (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Adam (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Agassiz (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguesse (1960) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ahmadzadeh et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Albouy et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Al-hasson & Ali (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Alquier et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Amand et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ananie et al. (2010) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 0 | 0% |
Anonyme (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Anonyme ([2015]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Aquarium de La Rochelle (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Arribas (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Arribas (1997) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Arthur et al. (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Attie & Jolivet (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Aubry et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Aumaître (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baguette & Schtickzelle (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baguette et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baguette (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baldi et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baliteau et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ballouard et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ballouard et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ballouard et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ballouard et al. (2023) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbancey (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Barbancey (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bardin et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baron (1987) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baudran & Gagnier (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Baux & Krieg-jacquier (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Béarez et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Beaucournu (1962) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Beauvieux et al. (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Belaud et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bence et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Alexanor, 3(2): 51-60.">Bernardi (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Berroneau (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bertrand & Drogou (2000) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bertrand et al. (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Billi (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Boisduval (1832-[1835]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boissieu & Chevrier (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bompar (1988) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bonaparte (1832-1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonelli et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bonhomme (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boreau (1849) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkhausen (1788) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boualit et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Boudot et al. (1987) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Boudrane (1983) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bour (1987) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bourgon (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Breuil (1982) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Bruneau de Miré (1997) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Burgeff (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Calviño et al. (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cambecèdes et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Candolle (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1830) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Carcaillet (1993) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Castanet & Cheylan (1979) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Caut et al. (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cayuela et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Celse et al. (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Celse et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Chambault et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Charbonnier et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Charpentier (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chemin & Gilette (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Chevreux & de Guerne (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cheylan et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Chrétien (1897) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ciccione (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ciccione (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Clech (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Clement & Chapalain (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Clements (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cogãlniceanu et al. (1998) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Colin (1992) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Colin (1994) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Emys orbicularis (Linné, 1758) - Statut ancien et présent. Annales de la Société des Sciences naturelle de la Charente-Maritime, 8(1): 67-73.">Collin de l'Hortet (1992) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Collin (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Combes & Clerc (1970) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Condamine et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Constantin et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Contejean (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Coton et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Coton et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cotrel & Grillet (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Courmont & Sousa (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Crampe & Barascud (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Crantz (1769) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosson Du Cormier & Guérin (1959) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Csabaï (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Cuénot & Mercier (1914) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Dalleau et al. (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Dapporto (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Daszkiewicz & Edel (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Daudin (1802) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
David et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
De Jong (1972) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Deflandre (1999) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Del Hoyo & Collar (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Delcroix et al. (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Delpon et al. (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Descimon et al. (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Descimon (1995) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Descimon (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Deslandes (1930) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Desmet (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Deso & Crouzet (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Deso (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Desse-Berset & Williot (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Desse-Berset (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Devaux (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dietz (2005) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Dohogne (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Doucet & Ruffoni (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
DREAL Alsace & MEDAD (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
DREAL Occitanie (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Dreux & Saint Girons (1951) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Baron (1998) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Duron (1981) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Duron (1982) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Duron (1983) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Duron (1984) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy & Duron (1985) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy et al. (1980) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy et al. (2000) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy (1967) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy (1983) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy (1986) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy (1988) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duguy (1989) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Duhaldeborde (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Dujardin (1951) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Escudié (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Eversmann (1836) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Favretto (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fay et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ficheux (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fitzinger (1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fizesan (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fourcroy (1785) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Franch et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fretey & Bour (1980) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fretey et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fretey (1980) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Fretey (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Frétey (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz & Havaš (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fruhstorfer (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fruhstorfer (1917) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gagno et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gaillard (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galibert et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gallardo & Penteriani (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gavory & Dommanget (1998) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gené (1839) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Genot et al. (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Geoffroy (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Georget (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Georget (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gerber (1972) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
GEREA & DIREN (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gérigny et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Geyer ([1828-1838]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Giacalone et al. (2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Giordano (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gmelin (1789) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gmelin (1791) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gonzalez et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gory (1995) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gouillard (1973) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Grand et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand (1989) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Grand (1989) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Grand (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Graves (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1851) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grillet & Thirion (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grisser (1987) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Guillon et al. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Gussone (1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guy et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Guyonneau (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Guyot & Devaux (1997) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Hämäläinen (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hansemann (1823) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Haworth (1802) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Helversen (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Hemming (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemming (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hennique et al. (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Herzberg (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Hoffmansegg [sic] (1804) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Houard & Archeray (2005) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Hunault & Kerbiriou (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Hunault (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Huot-daubremont et al. (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
ICZN (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingram (1915) | 1 | 0,05% | 1 | 0,41% | 0 | 0% | 1 | 0,41% |
Iorio (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Iorio (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Itrac-bruneau & Doucet (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Jandausch et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Jim et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Joos et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Jorcin et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Joshi et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Jourde & Perret (2006) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Karaa et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Kerguélen & Bock (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer & Veith (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Klein & Exinger (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Knijf (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Knoch (1781) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Knoch (1782) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Knoepffler (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1837) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolenati (1856) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuhn et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Kuhn (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Kuhn (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Kuntze (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Labbé (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lafranchis (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Laleu (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lamy (1978) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lang & Lecocq (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Langlois & Cayuela (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lantz (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeyrouse (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille & Godart (1819-[1824]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1804) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laufer & Nöllert (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Laurent (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laurenti (1768) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Moult (1945) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Legros & Puissauve (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Leraut (1990) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Letacq (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Delcroix (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lhotelin et al. (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Liardet & d'Auzon (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Liardet (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Liebart et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Linnaeus (1763) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Linné (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lisse & Delauje (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Loisier et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Loison (1989) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lopes-lima et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lorvelec & Pascal (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lorvelec et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lorvelec et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Lorvelec et al. (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Losinger (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Louisin & Probst (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Loveridge & Williams (1957) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyet et al. (2005) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Macé (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Magnanon et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Malm (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Maran (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Maran (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Marchand (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Marcou (1989) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Margońska (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Martin et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Martinez-Rica (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Martínez-silvestre et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mascort & Budó (2017) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mateo & Castroviejo (1991) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathon & Tomaselli (1959) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Matschie (1901) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mclachlan (1898) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
MEDD (2006) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MEDDE & MAAF (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Medde (2014) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Medetian & Miaud (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MEEDDAT & MAP (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Melvill (1873) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ménétriès (1859) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mennechez et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mérit et al. (2006) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Merleau et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MERLET & HOUARD (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mertens (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mezger (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Michallet et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Michel (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mignet et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Mignet et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Miller-Butterworth et al. (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Miquet (1996) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MNHN & Biotope, 2014 | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Moench (1794) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1808) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1893-1896) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Morizet (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
MTES & MAA (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Müller (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Nakamura et al. (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Natchev et al. (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Naulleau et al. (1998) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Nekrasova et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Némoz & Bertrand (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Nevé et al. (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Nickerl (1850) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Nikolskii (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nilsson-Ortman & Johansson (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Noel et al. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Oberthür (1898) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pafilis & Kapsalas (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Palacios et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Paradis et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pascal & Lorvelec (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pasco et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pedall et al. (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Peltier & Chevreau (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Perry et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Philippot & Georges (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Phillips (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Piazza (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pilard et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pilard (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Poirel (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Pöschel et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Poudré et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Prato et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Prévost & Mougin (1970) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Prié et al. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Primus (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Probst (1997) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Probst (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puechmaille et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve & Dupont (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Bardin & Escuder (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Cohen, Barthelemy & Reygnaud (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, De Massary, Marty & Pichenot (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Dupont & Lambert-L. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Dupont & Lambert-L. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Dupont & Lambert-L. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve, Haffner & Khun (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Legros & Dupont (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Legros & Dupont (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve, Legros & Dupont (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve, Legros, Kerbiriou & Marmet (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Puissauve (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rafinesque (1810) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Reichenbach & Reichenbach (1909) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Remsen et al. (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Renet et al. (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Revuelta et al. (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ribbe (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Riina et al. (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rimblot et al. (1985) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Roček et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
ROGEONR. & SORDELLO (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Roos (2000) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rouy (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruedi et al. (2002) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ruffoni (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Rüppell (1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sansault et al. (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Schneider (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulze (1776) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schur (1866) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Secchi (1999) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Selys & Longchamps (1840) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys-Longchamps & Hagen (1850) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan (1976) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Servan (1986) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Shaver et al. (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
SHF (2019) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Sibthorp & Smith (1806-1809) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Sonsino (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
SORDELLO (2012) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Soulsby (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spengler (1793) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spuler (1901-1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Staudinger & Rebel (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Staudinger (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Stempffer (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tellez & Dommanget (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Temminck et al. (1820-1840) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ternois & Barande (2005) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thibault et al. (2000) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thibault et al. (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thibault et al. (2023) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thibault (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thienpont (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thienpont (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thienpont (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thienpont (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thienpont (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thirion & Dore (2001) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thirion et al. (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thirion et al. (2024) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thomas (2015) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Thunberg & Becklin (1791) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Todisco et al. (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Toïgo et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Toledo et al. (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Torres et al. (2008) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Trotignon (2022) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Tutin et al. (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
UICN France, MNHN, LPO, SEOF & ONCFS. (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Uicn et al. (2020) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Une et al. (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Valentin et al. (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Van Halder & Jourdain (2010) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Vandelli (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vander & Linden (1825) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Veríssimo et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Verity (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verity (1932) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verreaux & Des Murs (1860) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Vieillot (1823[1822]) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Vigne & Pascal (2003) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Viricel (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Virion (2018) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Vittorio et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Waayers et al. (2011) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Wagler (1830) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Wagner (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wahl & Barbraud (2005) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ware et al. (2007) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Ware et al. (2016) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Warren (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Wencel (2000) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Wermuth (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Werneburg (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Zakharov et al. (2004) | 1 | 0,05% | 1 | 0,41% | 1 | 0,41% | 1 | 0,41% |
Zenboudji et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |