Espèces disparues
359 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) | 78 | 8,92% | 44 | 23,4% | 38 | 21,71% | 38 | 21,71% |
Funk et al. (2007) | 27 | 3,09% | 5 | 2,66% | 5 | 2,86% | 5 | 2,86% |
Aulagnier et al. (2017) | 26 | 2,97% | 24 | 12,77% | 24 | 13,71% | 23 | 13,14% |
Christenhusz (2009) | 23 | 2,63% | 12 | 6,38% | 12 | 6,86% | 12 | 6,86% |
Bernard (2015) | 21 | 2,4% | 17 | 9,04% | 17 | 9,71% | 17 | 9,71% |
Fournet (2002) | 21 | 2,4% | 17 | 9,04% | 17 | 9,71% | 13 | 7,43% |
Linnaeus (1758) | 19 | 2,17% | 5 | 2,66% | 5 | 2,86% | 4 | 2,29% |
Delannoye et al. (2015) | 13 | 1,49% | 7 | 3,72% | 7 | 4% | 7 | 4% |
Feldmann (2012) | 12 | 1,37% | 7 | 3,72% | 7 | 4% | 7 | 4% |
Acevedo-Rodríguez & Strong (2012) | 8 | 0,92% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Prado & Moran (2008) | 8 | 0,92% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Reverté et al. (2023) | 8 | 0,92% | 8 | 4,26% | 8 | 4,57% | 8 | 4,57% |
Rinaldi (2016) | 8 | 0,92% | 8 | 4,26% | 8 | 4,57% | 4 | 2,29% |
Falkner et al. (2002) | 7 | 0,8% | 4 | 2,13% | 3 | 1,71% | 3 | 1,71% |
Gargominy et al. (2011) | 7 | 0,8% | 6 | 3,19% | 4 | 2,29% | 4 | 2,29% |
Lessona (1880) | 7 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Carzon et al. (2016) | 6 | 0,69% | 6 | 3,19% | 6 | 3,43% | 3 | 1,71% |
Dillenberger & Kadereit (2014) | 6 | 0,69% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Estrade et al. (2016) | 6 | 0,69% | 6 | 3,19% | 6 | 3,43% | 3 | 1,71% |
Speight (2013) | 6 | 0,69% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Uicn et al. (2017) | 6 | 0,69% | 6 | 3,19% | 6 | 3,43% | 5 | 2,86% |
Derrick et al. (1987) | 5 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamy & Pointier (2018) | 5 | 0,57% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Levesque & Delcroix (2018) | 5 | 0,57% | 5 | 2,66% | 5 | 2,86% | 5 | 2,86% |
Belfan & Conde (2016) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Bouchet & Pointier (1998) | 4 | 0,46% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Brulin (2016) | 4 | 0,46% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Clements (2012) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Feldmann (2014) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Gasper et al. (2016) | 4 | 0,46% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Latham (1794) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Dusoulier (2015) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Pallas (1778) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin (2010) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Remsen et al. (2013) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
UICN Comité français, OFB & MNHN (2021) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Uicn et al. (2015) | 4 | 0,46% | 4 | 2,13% | 4 | 2,29% | 4 | 2,29% |
Aulagnier (2009) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 2 | 1,14% |
Béarez et al. (2017) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Blanco (2013) | 3 | 0,34% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Duméril (1865) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Groves & Grubb (2011) | 3 | 0,34% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Kerney & Cameron (1999) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 2 | 1,14% |
Kurtto (1981) | 3 | 0,34% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Müller & Henle (1841) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Munzinger et al. (2016) | 3 | 0,34% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Questel & Le Quellec (2012) | 3 | 0,34% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Rasmont & Wood (2024) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Schuiteman & Chase (2015) | 3 | 0,34% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Verdcourt (1987) | 3 | 0,34% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Véron et al. (2021) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 3 | 1,71% |
Welter-schultes (2012) | 3 | 0,34% | 3 | 1,6% | 3 | 1,71% | 2 | 1,14% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard et al. (2014) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Bloch & Schneider (1801) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Braun et al. (2019) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Brölemann (1909) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Brulin (2018) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Cambecèdes et al. (2012) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Cecchi & Selvi (2015) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Charrassin (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Charrassin (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Cochard et al. (2019) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Coomans (1967) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cramer ([1779]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cyrillo (1787) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
[Denis & Schiffermüller] (1775) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Dickinson & Remsen (2013) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Drivas & Jay (1997) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Faria et al. (2013) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Faure et al. (2008) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Fauvel (1883) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Fernandez-Carvalho et al. (2013) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Fischer (1884) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Foddai & Minelli (1999) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Fournier (1934-1940) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2009) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Gargominy (2011-2023) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Geoffroy & Iorio (2009) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Hamon (1953) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Hauk et al. (2003) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Hausmann & Viidalepp (2012) | 2 | 0,23% | 2 | 1,06% | 0 | 0% | 2 | 1,14% |
Henderson & Breuil (2012) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Hery et al. (2020) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Daszkiewicz (2001) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Iorio et al. (2023) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Lafranchis (2014) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Lafranchis (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Lagarde (2008) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Linnaeus (1753) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2007) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 0 | 0% |
Maillaud et al. (2015) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Massemin et al. (2009) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Mazancourt et al. (2019) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Meigen (1822) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaud (1829) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller & Wilson (1997) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Morat et al. (2012) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Moutou (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Nyakatura & Bininda-Emonds (2012) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Oberthür (1910) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pallas (1773) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Pichon & Thomassin (2005) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pichon et al. (2007) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pichon (2007) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pointier et al. (1977) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Prout (1934-1939) | 2 | 0,23% | 2 | 1,06% | 0 | 0% | 2 | 1,14% |
Questel (2020) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Ramage (2017) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Rambur (1858-[1866]) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau-desvoidy (1827) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Rönkä et al. (2016) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Spitz et al. (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Stoetzel et al. (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Thoisy & Bordin (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
UICN France & MNHN (2013) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Uicn et al. (2018) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 2 | 1,14% |
Urtizberea (2016) | 2 | 0,23% | 2 | 1,06% | 2 | 1,14% | 1 | 0,57% |
Vieweg (1790) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema et al. (2018) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Yokoyama (2013) | 2 | 0,23% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Amyot & Audinet-Serville (1843) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Anonyme. (2012) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Arthur & Lemaire (2015) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Aublet (1775) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Aubouin et al. (2016) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Badré (2008b) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Bagny et al. (2009) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bangy et al. (2009) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Belkin et al. (1965) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bence et al. (2016) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Benson et al. (1975) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Benson (1967) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Bikaeff (2002) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Billi et al. (2011) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Bloch & Schneider (1801) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Body (2021) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Boisduval (1840) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bojanus (1827) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1823) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1823) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordin et al. (2021) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Bot et al. (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Bourguignat (1877) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousses et al. (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2009) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Brown (2008) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Brunhes (1977) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunhes (1979) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1846) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carnevali et al. (2003) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carrillo (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Carte (1866) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Catzeflis (2012) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chiron & Bellone (2005) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Clergeau et al. (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Clergeau et al. (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Copeland (1932) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Cremers & Boudrie (2007) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1864) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1816) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Daltry & Gray (1988) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
David & Lucas (2017) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Deblock (1966) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Deniau & Provost (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Des et al. (2021) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Deshayes (1863) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Dewynter & Claessens (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Dewynter et al. (2019) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Dewynter et al. (2021) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Dietz & Kiefer (2015) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Dijkstra et al. (2015) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Döll (1843) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Dupont (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dusoulier & Lupoli (2006) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Erxleben (1777) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2007) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1805) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1954) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Fourcroy (1785) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2005) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Galliard (1927) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1928) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (1996) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Gaudin (1828) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerber (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Gibson (2001) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Gill (1995) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Gilot et al. (1992) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Giraud-Audine et al. (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Glynn et al. (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Godart (1822-[1824]) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Godineau & Pain (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Grand & Boudot (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Grand et al. (2014) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Gray (1821) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gueldenstaedt (1770) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamon (1956) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartert (1914) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Hayasaka (2012) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Heller (1916) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Hemming (1964) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hermann (1779) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Héros et al. (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Hoffmansegg [sic] (1804) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Houard & Jaulin (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Houard (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Hübner ([1790-1833]) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hume (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Huvier et al. (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Iorio & Racine (2022) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Iorio et al. (2022) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jameson et al. (2019) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jansen & Cheke (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jarrett & Shirihai (2014) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Jay et al. (2009) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jayson et al. (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jeffreys (1830) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones et al. (2019) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Jordan (1895) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Joshi et al. (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayser et al. (2019) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Keith et al. (1999) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Keith et al. (2006) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Keith et al. (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Keith (2003) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kitchener et al. (2017) | 1 | 0,11% | 1 | 0,53% | 0 | 0% | 1 | 0,57% |
Lafon (1953) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lair (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Laurenti (1768) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Le Goff et al. (2013) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Le Maitre & Chadee (1983) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure (1979) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Lescure (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Levesque & Yesou (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Linné (1766) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Louette & Cousin (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Maibach et al. (1994) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Mannings et al. (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Marboutin et al. (2006) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Marie & Bossin (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin et al. (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Mary (2017) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Masselot & Brulin (2001) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Matschie (1901) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Meurgey & Ramage (2020) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Monsecour & Monsecour (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Morelet (1851) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Moricand (1837) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mothiron (2001) | 1 | 0,11% | 1 | 0,53% | 0 | 0% | 1 | 0,57% |
Müller (1774) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1785) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1926) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Mulochau et al. (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Murray (1784) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nedeljković et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicholson et al. (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Nyman (1882) | 1 | 0,11% | 1 | 0,53% | 0 | 0% | 1 | 0,57% |
Olson & Warheit (1988) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Oriani (2014) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Orrell (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
øllgaard (2012) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Oueslati & Duvivier (2016) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pallas (1771) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pascal & Melin (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Paulian (1998) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Peters (1864) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pinchon (1976) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Poey (1858-61) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pointier & Théron (2006) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pointier (2008) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Polhill (1990) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pool (2013) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Poupin et al. (2013) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Poupin (2015) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Powell & Henderson (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Prado & Windisch (2000) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Prévost & Mougin (1970) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Pteridophyte Phylogeny Group (2016) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Questel (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Rafinesque (1820) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1958) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Reed (1968) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Reinert et al. (2004) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Revilliod (1914) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Ridgway (1893) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Roux (2009) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Ruffoni et al. (2024) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Rüppell (1842) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Say (1817) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sclater (1866) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sculfort & Dewynter (2024) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Senevet (1937) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Snak et al. (2016) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Speight (2018) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Stahl et al. (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Steindachner (1865) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Strobl (1909) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Talaga et al. (2015) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tapiero et al. (2017) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Temminck (1824-1825) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tenore (1811-1815) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2014) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Thoisy et al. (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 0 | 0% |
Toledo (2010) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Tröndlé & Boutet (2009) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Uicn et al. (2015) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vandel (1922) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vergonzanne (1977) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vigne & Pascal (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vigne & Pascal (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vigne et al. (2003) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vigne (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vigne (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vigne (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vigne (2003) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Vorimore et al. (2021) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Weimerskirch et al. (2009) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Weisler et al. (2006) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Werkhoven (1986) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Wewalka et al. (2023) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Withers (2017) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Witt & Ronkay (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2007) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |
Zimmermann (1780) | 1 | 0,11% | 1 | 0,53% | 1 | 0,57% | 1 | 0,57% |