Espèces terrestres des îles subantarctiques
1090 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) | 429 | 6,47% | 192 | 17,47% | 187 | 18,21% | 185 | 17,75% |
Roux (2012) | 392 | 5,91% | 67 | 6,1% | 66 | 6,43% | 66 | 6,33% |
Hullé et al. (2018) | 192 | 2,9% | 167 | 15,2% | 165 | 16,07% | 151 | 14,49% |
Uicn et al. (2015) | 137 | 2,07% | 132 | 12,01% | 131 | 12,76% | 120 | 11,52% |
Fournet (2002) | 131 | 1,98% | 116 | 10,56% | 116 | 11,3% | 116 | 11,13% |
Aptroot et al. (2011) | 127 | 1,92% | 85 | 7,73% | 85 | 8,28% | 85 | 8,16% |
Hullé & Vernon (2021) | 94 | 1,42% | 84 | 7,64% | 82 | 7,98% | 77 | 7,39% |
Ros et al. (2013) | 89 | 1,34% | 40 | 3,64% | 39 | 3,8% | 37 | 3,55% |
Hill et al. (2006) | 88 | 1,33% | 18 | 1,64% | 17 | 1,66% | 16 | 1,54% |
Deharveng (1981) | 74 | 1,12% | 72 | 6,55% | 68 | 6,62% | 72 | 6,91% |
Frenot et al. (2001) | 68 | 1,03% | 60 | 5,46% | 58 | 5,65% | 60 | 5,76% |
Hodgetts & Lockhart (2020) | 57 | 0,86% | 55 | 5% | 53 | 5,16% | 52 | 4,99% |
Voisin et al. (2017) | 53 | 0,8% | 53 | 4,82% | 42 | 4,09% | 53 | 5,09% |
Bonnet (1977) | 50 | 0,75% | 39 | 3,55% | 35 | 3,41% | 31 | 2,98% |
Deflandre (1927) | 48 | 0,72% | 31 | 2,82% | 30 | 2,92% | 21 | 2,02% |
Hullé et al. (2003) | 46 | 0,69% | 42 | 3,82% | 42 | 4,09% | 40 | 3,84% |
Hequet & Le Corre (2010) | 45 | 0,68% | 37 | 3,37% | 37 | 3,6% | 36 | 3,45% |
Hequet et al. (2009) | 45 | 0,68% | 37 | 3,37% | 37 | 3,6% | 36 | 3,45% |
MacKee (1994) | 45 | 0,68% | 37 | 3,37% | 37 | 3,6% | 36 | 3,45% |
Frenot et al. (2005) | 44 | 0,66% | 35 | 3,18% | 35 | 3,41% | 34 | 3,26% |
Carcaillet (1993) | 42 | 0,63% | 38 | 3,46% | 37 | 3,6% | 37 | 3,55% |
Jolinon (1987) | 42 | 0,63% | 36 | 3,28% | 36 | 3,51% | 36 | 3,45% |
Hébrard (1970) | 41 | 0,62% | 12 | 1,09% | 12 | 1,17% | 12 | 1,15% |
Heger et al. (2009) | 40 | 0,6% | 30 | 2,73% | 24 | 2,34% | 25 | 2,4% |
Grolle (2002) | 39 | 0,59% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Linnaeus (1758) | 37 | 0,56% | 13 | 1,18% | 13 | 1,27% | 12 | 1,15% |
Thécamoebiens du Sol". Hermann, Paris. 103pp.">Bonnet & Thomas (1960) | 36 | 0,54% | 27 | 2,46% | 20 | 1,95% | 21 | 2,02% |
Elix & McCarthy (1998) | 36 | 0,54% | 31 | 2,82% | 31 | 3,02% | 31 | 2,98% |
Bell (1982) | 35 | 0,53% | 27 | 2,46% | 26 | 2,53% | 27 | 2,59% |
Vincke et al. (2004) | 34 | 0,51% | 21 | 1,91% | 18 | 1,75% | 19 | 1,82% |
Ochyra et al. (2008) | 33 | 0,5% | 10 | 0,91% | 8 | 0,78% | 10 | 0,96% |
Kuschel & Chown (1995) | 31 | 0,47% | 13 | 1,18% | 13 | 1,27% | 11 | 1,06% |
Morrone (1998) | 31 | 0,47% | 13 | 1,18% | 13 | 1,27% | 11 | 1,06% |
Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1884) | 30 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1993) | 29 | 0,44% | 21 | 1,91% | 21 | 2,04% | 20 | 1,92% |
Hugonnot et al. (2017) | 29 | 0,44% | 23 | 2,09% | 23 | 2,24% | 20 | 1,92% |
Schenck (1906) | 28 | 0,42% | 23 | 2,09% | 23 | 2,24% | 22 | 2,11% |
Boom et al. (2011) | 25 | 0,38% | 25 | 2,27% | 25 | 2,43% | 25 | 2,4% |
Evenhuis (1989) | 25 | 0,38% | 24 | 2,18% | 21 | 2,04% | 23 | 2,21% |
Starý & Block (1998) | 25 | 0,38% | 23 | 2,09% | 20 | 1,95% | 21 | 2,02% |
Deflandre (1928) | 24 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Ertz et al. (2017) | 24 | 0,36% | 24 | 2,18% | 24 | 2,34% | 24 | 2,3% |
Chown & Convey (2016) | 23 | 0,35% | 21 | 1,91% | 21 | 2,04% | 21 | 2,02% |
Etcheberry et al. (1987) | 23 | 0,35% | 13 | 1,18% | 13 | 1,27% | 10 | 0,96% |
Ledoux (1991) | 23 | 0,35% | 23 | 2,09% | 19 | 1,85% | 23 | 2,21% |
Uicn et al. (2017) | 23 | 0,35% | 23 | 2,09% | 23 | 2,24% | 22 | 2,11% |
Wiersema et al. (2018) | 23 | 0,35% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Ochi (1972) | 22 | 0,33% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
UICN Comité français, OFB & MNHN (2021) | 21 | 0,32% | 21 | 1,91% | 21 | 2,04% | 21 | 2,02% |
Linnaeus (1753) | 20 | 0,3% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Questel (2020) | 20 | 0,3% | 19 | 1,73% | 19 | 1,85% | 19 | 1,82% |
Séguy (1960) | 20 | 0,3% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Ramage (2017) | 19 | 0,29% | 18 | 1,64% | 18 | 1,75% | 18 | 1,73% |
Etcheberry & Abraham (2009) | 18 | 0,27% | 17 | 1,55% | 17 | 1,66% | 17 | 1,63% |
Fourdrigniez & Meyer (2008) | 18 | 0,27% | 15 | 1,36% | 15 | 1,46% | 15 | 1,44% |
Linnaeus (1753) | 18 | 0,27% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Maier (2010) | 18 | 0,27% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
O’Shea (2006) | 18 | 0,27% | 11 | 1% | 8 | 0,78% | 10 | 0,96% |
Thouvenot & Bardat (2010) | 18 | 0,27% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Vasselon et al. (2019) | 18 | 0,27% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Meurgey & Ramage (2020) | 17 | 0,26% | 17 | 1,55% | 17 | 1,66% | 17 | 1,63% |
Nesom (2009) | 17 | 0,26% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Questel & Le Quellec (2012) | 17 | 0,26% | 16 | 1,46% | 16 | 1,56% | 16 | 1,54% |
Véron et al. (2021) | 17 | 0,26% | 17 | 1,55% | 17 | 1,66% | 17 | 1,63% |
Yokoyama (2013) | 17 | 0,26% | 17 | 1,55% | 17 | 1,66% | 17 | 1,63% |
Ausilio & Zotier (1989) | 16 | 0,24% | 15 | 1,36% | 15 | 1,46% | 14 | 1,34% |
Barau et al. (2005) | 16 | 0,24% | 13 | 1,18% | 13 | 1,27% | 13 | 1,25% |
Lahr & Lopes (2009) | 16 | 0,24% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rinaldi (2016) | 16 | 0,24% | 16 | 1,46% | 16 | 1,56% | 16 | 1,54% |
Travé (1982) | 16 | 0,24% | 15 | 1,36% | 13 | 1,27% | 14 | 1,34% |
Uicn et al. (2015) | 16 | 0,24% | 15 | 1,36% | 15 | 1,46% | 14 | 1,34% |
Van Der Putten et al. (2010) | 16 | 0,24% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Bobrov & Mazei (2017) | 15 | 0,23% | 7 | 0,64% | 5 | 0,49% | 5 | 0,48% |
Denis (1947) | 15 | 0,23% | 10 | 0,91% | 10 | 0,97% | 9 | 0,86% |
Eaton (1875) | 14 | 0,21% | 10 | 0,91% | 10 | 0,97% | 6 | 0,58% |
Funk et al. (2007) | 14 | 0,21% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Lorvelec et al. (2007) | 14 | 0,21% | 14 | 1,27% | 14 | 1,36% | 14 | 1,34% |
Øvstedal & Gremmen (2009) | 14 | 0,21% | 13 | 1,18% | 13 | 1,27% | 13 | 1,25% |
Brotherus (1906) | 13 | 0,2% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Enderlein (1909) | 13 | 0,2% | 10 | 0,91% | 10 | 0,97% | 10 | 0,96% |
Levesque & Delcroix (2018) | 13 | 0,2% | 13 | 1,18% | 13 | 1,27% | 13 | 1,25% |
Meurgey (2011) | 13 | 0,2% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Munzinger et al. (2016) | 13 | 0,2% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Penard (1890) | 13 | 0,2% | 6 | 0,55% | 6 | 0,58% | 3 | 0,29% |
Ros et al. (2007) | 13 | 0,2% | 10 | 0,91% | 10 | 0,97% | 10 | 0,96% |
Tixier (1980) | 13 | 0,2% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Waterhouse (1875) | 13 | 0,2% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cardot (1916) | 12 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Carzon et al. (2016) | 12 | 0,18% | 12 | 1,09% | 12 | 1,17% | 12 | 1,15% |
Estrade et al. (2016) | 12 | 0,18% | 12 | 1,09% | 12 | 1,17% | 12 | 1,15% |
Fain (1974) | 12 | 0,18% | 12 | 1,09% | 8 | 0,78% | 10 | 0,96% |
Hodgetts et al. (2020) | 12 | 0,18% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jourdan & Mille (2006) | 12 | 0,18% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Remsen et al. (2013) | 12 | 0,18% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Thibaud (2017) | 12 | 0,18% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Vernon & Voisin (1991) | 12 | 0,18% | 8 | 0,73% | 8 | 0,78% | 7 | 0,67% |
Vincke et al. (2004) | 12 | 0,18% | 6 | 0,55% | 5 | 0,49% | 5 | 0,48% |
Voisin et al. (2016) | 12 | 0,18% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Abraham (2010) | 11 | 0,17% | 11 | 1% | 11 | 1,07% | 11 | 1,06% |
Bescherelle (1875) | 11 | 0,17% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Euro+Med (2006) | 11 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 11 | 0,17% | 7 | 0,64% | 7 | 0,68% | 4 | 0,38% |
Prévost & Mougin (1970) | 11 | 0,17% | 11 | 1% | 10 | 0,97% | 11 | 1,06% |
Van de Vijver et al. (1999) | 11 | 0,17% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Viette (1959) | 11 | 0,17% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Wallwork (1972) | 11 | 0,17% | 10 | 0,91% | 9 | 0,88% | 8 | 0,77% |
Aulagnier et al. (2017) | 10 | 0,15% | 9 | 0,82% | 9 | 0,88% | 8 | 0,77% |
Blakemore (2008) | 10 | 0,15% | 6 | 0,55% | 5 | 0,49% | 5 | 0,48% |
Bourzat & Monie (1977) | 10 | 0,15% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Eaton et al. (1879) | 10 | 0,15% | 6 | 0,55% | 6 | 0,58% | 4 | 0,38% |
Hullé et al. (2010) | 10 | 0,15% | 10 | 0,91% | 10 | 0,97% | 10 | 0,96% |
Jolinon (1985) | 10 | 0,15% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Jourdan (2020) | 10 | 0,15% | 10 | 0,91% | 10 | 0,97% | 10 | 0,96% |
Le Gallo (1952) | 10 | 0,15% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Ochyra (1993) | 10 | 0,15% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Penard (1902) | 10 | 0,15% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Pickard-Cambridge (1876) | 10 | 0,15% | 4 | 0,36% | 4 | 0,39% | 2 | 0,19% |
Pugh (2004) | 10 | 0,15% | 10 | 0,91% | 8 | 0,78% | 9 | 0,86% |
Schiner (1868) | 10 | 0,15% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Travé (2021) | 10 | 0,15% | 10 | 0,91% | 10 | 0,97% | 10 | 0,96% |
Bonnet (1965) | 9 | 0,14% | 8 | 0,73% | 8 | 0,78% | 5 | 0,48% |
Chown & Kuschel (1994) | 9 | 0,14% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Decloitre (1960) | 9 | 0,14% | 9 | 0,82% | 8 | 0,78% | 7 | 0,67% |
Desplanques & Hébrard (1972) | 9 | 0,14% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Dreux & Voisin (1969) | 9 | 0,14% | 7 | 0,64% | 7 | 0,68% | 6 | 0,58% |
Gargominy et al. (1996) | 9 | 0,14% | 9 | 0,82% | 9 | 0,88% | 9 | 0,86% |
Giebel (1876) | 9 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra et al. (2014) | 9 | 0,14% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Playfair (1918) | 9 | 0,14% | 5 | 0,45% | 4 | 0,39% | 4 | 0,38% |
Rocamora (2004) | 9 | 0,14% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Roux & Coll (2020) | 9 | 0,14% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Soubeyran et al. (2011) | 9 | 0,14% | 9 | 0,82% | 9 | 0,88% | 9 | 0,86% |
Subías (2004) | 9 | 0,14% | 9 | 0,82% | 8 | 0,78% | 9 | 0,86% |
Tostain et al. (2013) | 9 | 0,14% | 9 | 0,82% | 9 | 0,88% | 8 | 0,77% |
Vayssières et al. (2001) | 9 | 0,14% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Barré (2021) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Bouché (1982) | 8 | 0,12% | 6 | 0,55% | 6 | 0,58% | 5 | 0,48% |
Cambecèdes et al. (2012) | 8 | 0,12% | 6 | 0,55% | 5 | 0,49% | 6 | 0,58% |
Chattová et al. (2018) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Denux & Zagatti (2010) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Ellis et al. (2018) | 8 | 0,12% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Etienne (2005) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Monod & Dollfus (1932) | 8 | 0,12% | 7 | 0,64% | 7 | 0,68% | 5 | 0,48% |
Ochyra & Bednarek-ochyra (2017) | 8 | 0,12% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Rouy (1908) | 8 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tapolczai et al. (2017) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Tronquet (2014) | 8 | 0,12% | 8 | 0,73% | 8 | 0,78% | 8 | 0,77% |
Albouy & Richard (2017) | 7 | 0,11% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Borgato et al. (2020) | 7 | 0,11% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Flatberg et al. (2011) | 7 | 0,11% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
González-miguéns et al. (2021) | 7 | 0,11% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Grolle & Long (2000) | 7 | 0,11% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Hekking & Sipman (1988) | 7 | 0,11% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Hemsley (1885) | 7 | 0,11% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Morat et al. (2012) | 7 | 0,11% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Remaudière & Etienne (1988) | 7 | 0,11% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Schenck (1905) | 7 | 0,11% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Váňa et al. (2014) | 7 | 0,11% | 7 | 0,64% | 7 | 0,68% | 7 | 0,67% |
Aulagnier (2009) | 6 | 0,09% | 5 | 0,45% | 5 | 0,49% | 4 | 0,38% |
Béguinot (2012) | 6 | 0,09% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Belfan & Conde (2016) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Blockeel et al. (2010) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Chapuis et al. (2004) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Coste et al. (2008) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Deblock et al. (1960) | 6 | 0,09% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Deflandre (1929) | 6 | 0,09% | 2 | 0,18% | 1 | 0,1% | 1 | 0,1% |
Dreux & Voisin (1986) | 6 | 0,09% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Ellis et al. (2016) | 6 | 0,09% | 4 | 0,36% | 4 | 0,39% | 3 | 0,29% |
Fedosov et al. (2023) | 6 | 0,09% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gomy (2000) | 6 | 0,09% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Kieffer (1902) | 6 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 6 | 0,09% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Marchán et al. (2022) | 6 | 0,09% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Moser (1999) | 6 | 0,09% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Peck et al. (2014) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Safford & Hawkins (2013) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Theuerkauf et al. (2010) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Timaná et al. (2019) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 6 | 0,58% |
Wigginton (2009) | 6 | 0,09% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Ysnel & Ledoux (1988) | 6 | 0,09% | 6 | 0,55% | 6 | 0,58% | 5 | 0,48% |
Albouy et al. (2017) | 5 | 0,08% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Banks et al. (2006) | 5 | 0,08% | 4 | 0,36% | 4 | 0,39% | 1 | 0,1% |
Chattova et al. (2014) | 5 | 0,08% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Dalenius & Wilson (1958) | 5 | 0,08% | 3 | 0,27% | 0 | 0% | 3 | 0,29% |
Fauvel (1867) | 5 | 0,08% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jimenez & Suarez (2016) | 5 | 0,08% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jiménez-lópez et al. (2022) | 5 | 0,08% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Maillard (1978) | 5 | 0,08% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Mazei & Warren (2015) | 5 | 0,08% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mennema (1989) | 5 | 0,08% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mille et al. (2020) | 5 | 0,08% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Ochi (1982) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra (2003) | 5 | 0,08% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ogden (1983) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Papierok et al. (2016) | 5 | 0,08% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Perrie & Parris (2012) | 5 | 0,08% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Potin (2013) | 5 | 0,08% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Voisin et al. (2014) | 5 | 0,08% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Weimerskirch et al. (2009) | 5 | 0,08% | 5 | 0,45% | 5 | 0,49% | 5 | 0,48% |
Acevedo-Rodríguez & Strong (2012) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Barbraud et al. (2009) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Barre et al. (2009) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Barta & Cagáň (2006) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Bednarek-ochyra et al. (2018) | 4 | 0,06% | 2 | 0,18% | 1 | 0,1% | 1 | 0,1% |
Blockeel et al. (2009) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Bost et al. (2022) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 2 | 0,19% |
Castilho et al. (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Cazanove (2022) | 4 | 0,06% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Charrassin (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Charrassin (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Clarke (1971) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Clements et al. (2015) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 3 | 0,29% |
Clements (2012) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Davies, L. & Greene, S.W. (1976) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Delord et al. (2005) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Delord et al. (2008) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
[Denis & Schiffermüller] (1775) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Des et al. (2021) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Dujardin (1841) | 4 | 0,06% | 2 | 0,18% | 2 | 0,19% | 1 | 0,1% |
Ellis et al. (2015) | 4 | 0,06% | 4 | 0,36% | 2 | 0,19% | 4 | 0,38% |
Ellis et al. (2017) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Enderlein (1905) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Enderlein (1909) | 4 | 0,06% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Forster (1781) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Frahm (2010) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gandoger (1875) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1884) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaud (1952) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Gentry et al. (2004) | 4 | 0,06% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Gill (1995) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Gmelin (1789) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gomy et al. (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Gray (1821) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2004) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hammer (1958) | 4 | 0,06% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Heller (1916) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
IUCN (2013) | 4 | 0,06% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Jaeger et al. (2020) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Jarrett & Shirihai (2014) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Kieffer (1902-1904) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kieffer (1907-1911) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kojadinovic et al. (2007) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Kosakyan et al. (2012) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Le Cohu & Van de Vijver (2002) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Martiré & Rochat (2008) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
, 4: 321-360.">Matteri (1973) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Picard (2011) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Mitten (1876) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutou (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Ochyra & Poulsen (2003) | 4 | 0,06% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ochyra (1997) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pletzen van et Kok (1971) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Ponge et al. (2003) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Probst (1997) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 3 | 0,29% |
Roux (2013) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rouy (1899) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Salisbury (1796) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Savigny (1826) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Scheller (1974) | 4 | 0,06% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Soler-zamora et al. (2023) | 4 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sollman (2016) | 4 | 0,06% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Spitz et al. (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Thoisy & Bordin (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Urtizberea (2016) | 4 | 0,06% | 4 | 0,36% | 4 | 0,39% | 4 | 0,38% |
Van et al. (2002) | 4 | 0,06% | 4 | 0,36% | 2 | 0,19% | 4 | 0,38% |
Vincke et al. (2004) | 4 | 0,06% | 4 | 0,36% | 2 | 0,19% | 3 | 0,29% |
Abeyrama et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Aulagnier (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Azam (1893) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Badonnel (1947) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Barbraud et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Barbut & Voisin (2014) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Bardat et al. (2021) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Beaucournu-Saguez & Vernon (1990) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bellido et al. (1987) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beron (2022) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Bochaton et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Bonnet & Thomas (1955) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Boullet et al. (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Bricaud (2007) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bruggeman-Nannenga & Arts (2010) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Burneleau (1983) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Butaud (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Candolle (1815) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Carravieri et al. (2016) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Catzeflis (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Chapelin-Viscardi et al. (2010) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Chattova et al. (2017) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Chattová et al. (2021) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chau et al. (2020) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Coste & Ricard (1990) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Decloitre (1981) | 3 | 0,05% | 3 | 0,27% | 0 | 0% | 3 | 0,29% |
Del Hoyo & Collar (2014) | 3 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Delamare Deboutteville & Massoud (1966) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Dewynter (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Dillenberger & Kadereit (2022) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2012) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ellis et al. (2013) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ellis et al. (2013) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ellis et al. (2017) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
, 3: 249-270.">Enderlein (1903) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ertz et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Etienne & Vilardebó (1978) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Evenhuis (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Fairmaire (1849) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Ferlay et al. (2023) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Fournier (1934-1940) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fransén (2004) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fryday (2007) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Gasper et al. (2016) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Geer (1774) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gradstein & Ilkiu-Borges (2009) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand et al. (2014) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Grandjean (1955) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Guth (1971) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Gutierrez (1981) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Hammes & Putoa (1986) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Hooker (1875) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jeannenot (1955) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin et al. (1989) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Karlin et al. (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Klompen & Johnson (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Lee (1970) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Leidy (1879) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lescroel et al. (2009) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Lessona & Pollonera (1882) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Majestyk (2011) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Matile (1975) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mey (2010) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 3 | 0,29% |
Moench (1794) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier et al. (2009) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Montrouzier (1860) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nicolet (1847) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyman (1882) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochi (1980) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ochyra & Bednarek-ochyra (2013) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Øvstedal & Gremmen (2010) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Peck (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Ponchon et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Reichardt (1871) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Renault (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Ricard (1985) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Roux & coll (2022) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sagar (1991) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 0 | 0% |
Seguy (1965) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Seppelt (1991) | 3 | 0,05% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Strandtmann & Davies (1972) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Sundue et al. (2010) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Thiebot et al. (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Thouvenot et al. (2011) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tremblay & Cherel (2005) | 3 | 0,05% | 3 | 0,27% | 0 | 0% | 3 | 0,29% |
Uicn et al. (2020) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Váňa et al. (2010) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Van de Vijveret al. (2002) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Voisin et al. (2015) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Young (1971) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,29% |
Adamska & Grzywacz (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
André & Colas-belcour (1942) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme & Bosch (1950) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2014) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Arup et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Aubert de la Rüe (1932) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Aublet (1775) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Azab et al. (1972) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Badonnel (1970) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bartlett & Frahm (1983) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu & Rodhain (1990) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bednarek-Ochyra & Plášek (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bell et al. (1989) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bellemare & Brunelle (1950) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Benedetti et al. (2021) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 1 | 0,1% |
Berta & Churchill (2012) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Betsch & Massoud (1970) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Blockeel et al. (2007) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Blockeel et al. (2009) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Boggan et al. (1997) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bonfils (1969) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bonnet & Thomas (1960) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Bonnet (1959) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bonnet (1979) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Boreau (1857) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Borovec (1991) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer & Rivault (2003) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Brand et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Breton (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Brodier et al. (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bubani & Penzig (1901) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabanis (1875) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cash & Hopkinson (1909) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cash et al. (1915) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Cazanove et al. (2022) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cerkowniak et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chandebois (1958) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chartier et al. (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Cherel et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cherel et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Cochereau (1974) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Coulot & Rabaute (2016) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Couteyen & Papazian (2012) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Covarrubias (1968) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dadant & Etienne (1973) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Daly et al. (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
D'Amico (2001) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Daniel et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dastych (1999) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Decloitre (1968) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,1% |
Delarue (1988) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Denis (1921) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Denis (1922) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Diaz et al. (2009) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dickinson & Remsen (2013) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Dreux & Voisin (1984) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1987) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dreux & Voisin (1988) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dronneau & Wassmer (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dubois et al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ellis et al. (2012) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2014) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2015) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ellis et al. (2019) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1936) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ertz et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Etienne et al. (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Evenhuis & Barbotin (1977) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fauvel (1862) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1891) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fauvel (1903) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1903) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Féral et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fonteneau & Cook (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fontenot et al. (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Forsslund (1964) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fort & Barrière (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fourcroy (1785) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Frey (1948) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Frugone et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Fuentes-bazan et al. (2012) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gargominy et al. (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gomez & Voisin (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Gould (1844) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Grandjean (1957) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Green (1996) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Greene & Greene (1963) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Grenier & Godron (1850) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffiths & Florens (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Grosser et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Guillermet (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hale et al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hall (1900) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Hava (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Háva (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hentschel et al. (2007) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hindermeyer et al. (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hirschmann & Wisniewski (1988) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hoff & Cremers (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hooker & Wilson (1844) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hossain et al. (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Humeau et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Hunter (1967) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Husnot (1908) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyvönen (1991) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ignatov & Huttunen (2002) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ignatov et al. (2020) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Impact-mer (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Imshaug (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jagerskiold (1905) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
James (1875) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeannel (1947) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jiguet (2002) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Jiménez & Ochyra (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jones et al. (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jones et al. (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jung (1942) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Karadjian et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Karg (1997) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kerney & Cameron (1999) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Kieffer (1898) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner (1990) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuhl (1820) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuntze (1891) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lamarck (1779) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Laparie & Renault (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Le Gallo (1951) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Léotard & Chaline (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lemée (1953) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Leraut (1997) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescroel et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lions (1966) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,1% |
Lohmann (1907) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lubbock (1876) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lucas (1847) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Macquart (1835) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Magill (1982) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Manns & Anderberg (2007) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Marques et al. (1984) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Massé (1982) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Mays et al. (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Meganck et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Meyer (1819) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Milan (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mitten (1876) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat & Veillon (1985) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Muller et al. (2004) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nentwig & Kobelt (2010) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ochyra & Bednarek-Ochyra (1997) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ochyra et al. (1986) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Olson & Jouventin (1996) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pallas (1831) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. 2006 | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Paulian (1998) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pedersen (2005) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Peterson et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pisanu & Bain (1999) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pistil & Kontykowski (1974) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pócs (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pontoppidan (1763) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Presl & Presl (1822) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pugh & Scott (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pugh et al. (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pujade-Villar et al. (2007) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rakowski et al. (1981) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rambur (1829) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Raust & Sanford (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Reeve (1851-1854) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeves et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Reichenow (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Renault et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Reveal et al. (1991) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Riaux-Gobin & Compère (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Richters (1908) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridoux (1989) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Roberts (2014) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Robineau-Desvoidy (1841) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rognes & Blackith (1990) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Romero & Van de Vijver (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rooy et al. (2021) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rouhan et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Routtier et al. (2023) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux et al. (1983) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1897) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Saaristo & Tanasevitch (1996) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sabine (1818) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint et al. (1978) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Salmon (1964) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Salvin (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Savouré-Soubelet et al. (in prep.) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Schenck (1905) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenker (1986) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Scopoli (1771) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Searby & Jouventin (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Séguy (1954) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Serra-Tosio (1986) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Siljak-Yakovlev et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Soldati & Touroult (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Song et al. (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Spence & Ramsay (2005) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Spence (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Stahl et al. (1985) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Szederjesi et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Tavakilian & Chevillotte (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Temminck et al. (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tennyson et al. (2022) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Thériot (1924) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Thibault et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Thomas (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Thouvenot & Müller (2021) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tremblay & Cherel (2003) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Trouessart (1898) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Turcati (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Váňa & Gremmen (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Váňa & Long (2011) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vélain (1877) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Vidal & Vansteene (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Vilkamaa & Menzel (2019) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitt (1976) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitt (1979) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Voisin (1971) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Wainstein (1956) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1802) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallwork (1963) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallwork (1970) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Waugh & Weimerskirch (2003) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Wise (1970) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Wise (1974) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Withers & Chandler (2019) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Yang et al. (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Zander & Brinda (2021) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zander (2017) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zanetti et al. (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Abbayes (1931) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Abdel-kader & Barak (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Akl et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Allen et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Anonyme (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Arcangeli (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubouin et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bagnall (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Banfi et al. (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barre et al. (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Beatty et al. (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bellido & Dafonseca (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Belon & Mulsant (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Berland (1942) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Berton (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bertrand (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bester & Roux (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Błeszyński & Collins (1962) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bigot (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Billi (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blair (1934) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blair (1934) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blas (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bleeckere (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blockeel et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blockeel et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blockeel et al. (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Blyth (1841) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Blyth (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Body (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boie (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bondarenko & Kontrimavichus (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Boreau (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouget et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bournier & Mound (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bournier (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Bouteiller & Borsa (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brady (1910) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brandt (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brinda et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brindle (1971) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brindle (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Brindle (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Briones (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Burr (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Buyck et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres & Salamolard (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Callou (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Candolle (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carapelli et al. (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carapelli et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cariot & Saint-lager (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (1934) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Carpenter (1935) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cerkowniak et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chapuis et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapuis et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cheesman (1927) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cheesman (1928) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cherel & Boxshall (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Chopard (1924) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cibois et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Clemens (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cockerell (1911) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cohic (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cohu & Azémar (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Colijn et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Collier et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Commission de l’Avifaune Française (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Condamin (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Cowie (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crotch (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Damoiseau (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Daudin (1802) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Davies (1965) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock & Raush (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Debout (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Décloitre (1962) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Decloitre (1969) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Decloitre (1970) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Decloitre (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Decloitre (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Decloitre (1978) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Decloitre (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Decloitre (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deeming (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deflandre (1928) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Deflandre (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delfosse (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Meyer (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Delord et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Demay et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Devaud & Lebouvier (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dewynter et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dias et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Don (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dreux et al. (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Dulac (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebels (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrenberg (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ellis et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Enderlein (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Enderlein (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Evenhuis (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fabricius (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1850) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Falla (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallén (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feret et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferrer (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferrer-Suay et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Suay et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ferrer-Suay et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fife (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fife (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Finsch (1876) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Flora iberica | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Frauenfeld (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz-Sheridan & Portecop (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Fueßlin (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gadeau de Kerville (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
GARNOT (1826) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrouste & Hervé (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gassiole (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaudin (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gauthier-clerc & Lambert (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Genevois (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Geoffroy (1762) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Giani (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gibb et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Global Carex Group (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Goetghebuer (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goeze (1777) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Golemansky (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gonzales et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
González-Miguéns et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gould (1838) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Gray (1872) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Greeff (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grisebach (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle & Onraedt (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Groves & Grubb (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guglielmone et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Guiguen et al. (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Gunnerus (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Haliday (1834) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hammer (1972) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Harrison (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hartig (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartwich (1964) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hava & Poussereau (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hayashi (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hebard (1933) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hebard (1933) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hébrard (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Heppner (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Heylen et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hinton (1941) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoddle et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hoff (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1791) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Holyoak & Pedersen (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Holyoak (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hombron & Jacquinot (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Honey & Scoble (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hughes & Goodman (1969) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Hughes (1955) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Hunter (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Hustache (1920) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hynes (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ingels et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Iwatsuki (1970) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jaeger et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jarrige & Voisin (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jeannel (1953) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Johannsen (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson et al. (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Jordan & Fourreau (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin & Roux (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Justine et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karsch (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaszab (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kaszab (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Koch (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolenati (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kondratyuk et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kosakyan et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kumar et al. (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Kuschel (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacomme (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lafranchis (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lafranchis (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lagarde (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lamarck & Candolle (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
.">Lambret & Lebouvier (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lara et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Le Corre & Jouventin (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Le Maitre & Chadee (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ledoux & Hallé (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lejeune & Courtois (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemagnen (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescroel & Bost (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lesson (1825) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Li et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lieftinck (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lieftinck (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lieutard (1893) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Linnaeus (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeblich & Tappan (1961) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Louwhoff & Elix (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lubbock (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Macaigne & Perez-eid (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Madec & Bellido (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Malloch (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Malloch (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mammola & Milano (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Manns & Anderberg (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marinov et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marinov et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marinov et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Marion & Marion (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Martin-vega et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Massé et al. (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Massé (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mathews & Iredale (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
McFarland (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Medway (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meigen (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Menezes et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Menezes et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Menzel & Vilkamaa (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mercier (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mériguet & Zagatti (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meyer et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Meyrick (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Michelet et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Miégeville (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Minot (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Miskelly (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moench (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morrison (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moubayed-Breil et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mougin (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Moulton (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1776) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Munari (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Murphy & Harper (1916) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Murphy (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Muru et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Mutel (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Najt (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Naumann (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Naurois (1978) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nebbak et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nentwig et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Nicolet (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ochyra et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ogden & Živković (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Olivier (1791-[1792]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
O'reilly (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
øvstedal & Gremmen (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Osuji (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Osuji (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
pallas (1764) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Papazian et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Parnaudeau (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pascal et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pavlíček & Csuzdi (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Penard (1904) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Penard (1910) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Perrin et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Persoon (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Piippo (1983) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinaud et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Porfirio-sousa et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Porto & Pérez-gonzález (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Poussereau et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Prevost (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Price & Ellis (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Pteridophyte Phylogeny Group (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Quindroit & Lemoine (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Quindroit (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rageau (1956) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rageau (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rehn (1949) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Reichardt (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Remillet (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinheimer (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rheinheimer (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ris (1915) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Robert et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Robertson (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rosenbaum et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rossi (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschikd (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschild (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouhan (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Roux & Martinez (1987) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Rouy & Foucaud (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruecker (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ruys & Coord (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Salmon (1943) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Salmon (1949) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Samways (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sardet et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schaefer et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Scheller (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schiebel (1910) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schlesak et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schött (1902) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Schramm et al. (2014) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Schrank et al. (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank (1781) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Séchet & Noël (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sennen (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaaya (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shahhosseini (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shinonaga et al. (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Shiraki (1906) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siddaiah & Kujur (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Siroux (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Skierska (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Smith (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Solem (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Soubeyran (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stahl & Weimerskirch (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Stahl et al. (1984) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Stanek et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Starý et al. (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stefanescu et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Steffan (1972) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stein (1911) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Stierlin (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler & Crandall-Stotler (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Sueur (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taranek (1881) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Theodorides (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thibaud & Najt (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thiebot et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiebot et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thomas (1959) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot & Bardat (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Thouvenot (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Timaná (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tonnoir (1940) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tourlan (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Touroult et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Trehen & Voisin (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Tronquet (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tunstall (1880) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vaillant (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Van de Vijver et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vana & Gremmen (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vanderwerf et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vanhöffen (1912) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viane (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viane (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viette (1949) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Viette (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Villars (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villot (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vincent & Voisin (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vincke et al. (2006) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,1% |
Vinson (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Voisin (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Vollmann (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vourc'h et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wailes & Penard (1911) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Wailes (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallwork (1962) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Weimerskirch & Jouventin (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Weimerskirch et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Westwood (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiggers (1780) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Willem (1901) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Wilson (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zander & Hedderson (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zander (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zanetti et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Zhao et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |
Ziffer-Berger et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,1% |