Espèces de Saint-Pierre-et-Miquelon
Toutes les espèces de Saint-Pierre-et-Miquelon
2076 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Courtecuisse (2009) | 1782 | 8.49% | 282 | 9.34% | 277 | 9.84% | 276 | 9.73% |
Tison et al. (2014) | 1160 | 5.53% | 531 | 17.58% | 487 | 17.31% | 443 | 15.62% |
Roux (2012) | 623 | 2.97% | 136 | 4.5% | 134 | 4.76% | 134 | 4.72% |
Abraham (2021) | 346 | 1.65% | 303 | 10.03% | 303 | 10.77% | 299 | 10.54% |
Linnaeus (1758) | 282 | 1.34% | 62 | 2.05% | 62 | 2.2% | 57 | 2.01% |
Hill et al. (2006) | 271 | 1.29% | 132 | 4.37% | 130 | 4.62% | 130 | 4.58% |
Ros et al. (2013) | 250 | 1.19% | 154 | 5.1% | 152 | 5.4% | 152 | 5.36% |
Etcheberry & Abraham (2009) | 230 | 1.1% | 192 | 6.36% | 192 | 6.82% | 180 | 6.35% |
Hodgetts & Lockhart (2020) | 211 | 1.01% | 207 | 6.85% | 203 | 7.21% | 203 | 7.16% |
Etcheberry et al. (1987) | 192 | 0.91% | 147 | 4.87% | 145 | 5.15% | 145 | 5.11% |
Abraham (2010) | 176 | 0.84% | 150 | 4.97% | 148 | 5.26% | 149 | 5.25% |
Levesque & Delcroix (2018) | 159 | 0.76% | 152 | 5.03% | 147 | 5.22% | 152 | 5.36% |
Fournet (2002) | 147 | 0.7% | 128 | 4.24% | 128 | 4.55% | 116 | 4.09% |
Hugonnot et al. (2017) | 140 | 0.67% | 102 | 3.38% | 102 | 3.62% | 98 | 3.46% |
Le Gallo (1952) | 136 | 0.65% | 77 | 2.55% | 77 | 2.74% | 77 | 2.72% |
UICN Comité français, OFB & MNHN (2021) | 120 | 0.57% | 120 | 3.97% | 120 | 4.26% | 116 | 4.09% |
Uicn et al. (2017) | 119 | 0.57% | 112 | 3.71% | 109 | 3.87% | 105 | 3.7% |
Questel (2020) | 115 | 0.55% | 110 | 3.64% | 107 | 3.8% | 107 | 3.77% |
Hacala et al. (2024) | 109 | 0.52% | 109 | 3.61% | 109 | 3.87% | 109 | 3.84% |
Nelson-Smith et al. (2014) | 99 | 0.47% | 74 | 2.45% | 74 | 2.63% | 74 | 2.61% |
Yokoyama (2013) | 89 | 0.42% | 73 | 2.42% | 73 | 2.59% | 71 | 2.5% |
Christenhusz et al. (2019) | 88 | 0.42% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Questel & Le Quellec (2012) | 85 | 0.41% | 80 | 2.65% | 79 | 2.81% | 77 | 2.72% |
Rinaldi (2016) | 84 | 0.4% | 80 | 2.65% | 80 | 2.84% | 44 | 1.55% |
Linnaeus (1753) | 82 | 0.39% | 57 | 1.89% | 53 | 1.88% | 46 | 1.62% |
Bousquet (2012) | 66 | 0.31% | 64 | 2.12% | 58 | 2.06% | 64 | 2.26% |
Moreau et al. (2023) | 66 | 0.31% | 0 | 0% | 0 | 0% | 0 | 0% |
Remsen et al. (2013) | 66 | 0.31% | 62 | 2.05% | 62 | 2.2% | 60 | 2.12% |
Elder & Abraham (2012) | 65 | 0.31% | 65 | 2.15% | 65 | 2.31% | 65 | 2.29% |
Roux (1984) | 65 | 0.31% | 59 | 1.95% | 58 | 2.06% | 54 | 1.9% |
Uicn et al. (2015) | 65 | 0.31% | 63 | 2.09% | 63 | 2.24% | 48 | 1.69% |
Béarez et al. (2017) | 63 | 0.3% | 63 | 2.09% | 63 | 2.24% | 63 | 2.22% |
Carzon et al. (2016) | 63 | 0.3% | 60 | 1.99% | 60 | 2.13% | 33 | 1.16% |
Estrade et al. (2016) | 63 | 0.3% | 60 | 1.99% | 60 | 2.13% | 33 | 1.16% |
Tronquet (2014) | 63 | 0.3% | 63 | 2.09% | 61 | 2.17% | 58 | 2.05% |
Linnaeus (1753) | 60 | 0.29% | 33 | 1.09% | 31 | 1.1% | 28 | 0.99% |
Ros et al. (2007) | 58 | 0.28% | 31 | 1.03% | 31 | 1.1% | 29 | 1.02% |
Belfan & Conde (2016) | 57 | 0.27% | 55 | 1.82% | 55 | 1.95% | 54 | 1.9% |
Le Gallo (1951) | 53 | 0.25% | 30 | 0.99% | 30 | 1.07% | 28 | 0.99% |
MacKee (1994) | 53 | 0.25% | 44 | 1.46% | 44 | 1.56% | 40 | 1.41% |
Hequet & Le Corre (2010) | 52 | 0.25% | 43 | 1.42% | 43 | 1.53% | 39 | 1.38% |
Hequet et al. (2009) | 52 | 0.25% | 43 | 1.42% | 43 | 1.53% | 39 | 1.38% |
Noblecourt (2016) | 49 | 0.23% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Burel et al. (2019) | 44 | 0.21% | 44 | 1.46% | 44 | 1.56% | 42 | 1.48% |
Simian et al. (2022) | 44 | 0.21% | 44 | 1.46% | 44 | 1.56% | 44 | 1.55% |
Hindermeyer et al. (2007) | 42 | 0.2% | 40 | 1.32% | 37 | 1.31% | 39 | 1.38% |
Le Gallo (1949) | 40 | 0.19% | 27 | 0.89% | 27 | 0.96% | 26 | 0.92% |
Delamare et al. (1888) | 38 | 0.18% | 4 | 0.13% | 1 | 0.04% | 4 | 0.14% |
Grolle & Long (2000) | 38 | 0.18% | 27 | 0.89% | 27 | 0.96% | 27 | 0.95% |
Frenot et al. (2001) | 36 | 0.17% | 32 | 1.06% | 31 | 1.1% | 26 | 0.92% |
Breton (2014) | 35 | 0.17% | 33 | 1.09% | 33 | 1.17% | 32 | 1.13% |
Elix & McCarthy (1998) | 35 | 0.17% | 26 | 0.86% | 26 | 0.92% | 26 | 0.92% |
Albouy & Richard (2017) | 34 | 0.16% | 31 | 1.03% | 31 | 1.1% | 25 | 0.88% |
Uicn et al. (2020) | 34 | 0.16% | 34 | 1.13% | 34 | 1.21% | 31 | 1.09% |
Wiersema et al. (2018) | 34 | 0.16% | 11 | 0.36% | 11 | 0.39% | 8 | 0.28% |
Gray (1821) | 30 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll (2020) | 30 | 0.14% | 10 | 0.33% | 10 | 0.36% | 10 | 0.35% |
Cabioc'h & Floc'h (2014) | 29 | 0.14% | 24 | 0.79% | 24 | 0.85% | 23 | 0.81% |
Salisbury (1796) | 29 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Béguinot (2012) | 28 | 0.13% | 19 | 0.63% | 19 | 0.68% | 12 | 0.42% |
Jolinon (1987) | 28 | 0.13% | 26 | 0.86% | 26 | 0.92% | 24 | 0.85% |
Tostain et al. (2013) | 28 | 0.13% | 23 | 0.76% | 22 | 0.78% | 23 | 0.81% |
Derrick et al. (1987) | 27 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
[Denis & Schiffermüller] (1775) | 26 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
Euro+Med (2006) | 26 | 0.12% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Godet et al. (2010) | 26 | 0.12% | 26 | 0.86% | 26 | 0.92% | 26 | 0.92% |
Martin (2011) | 26 | 0.12% | 22 | 0.73% | 22 | 0.78% | 22 | 0.78% |
Albouy et al. (2017) | 25 | 0.12% | 23 | 0.76% | 23 | 0.82% | 21 | 0.74% |
Gmelin (1789) | 25 | 0.12% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Mertens & Wermuth (1960) | 25 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
Carcaillet (1993) | 24 | 0.11% | 23 | 0.76% | 22 | 0.78% | 20 | 0.71% |
Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1883) | 24 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts et al. (2020) | 23 | 0.11% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Leraut (2012) | 23 | 0.11% | 21 | 0.7% | 21 | 0.75% | 21 | 0.74% |
Armada (2018) | 22 | 0.1% | 18 | 0.6% | 18 | 0.64% | 17 | 0.6% |
Aulagnier (2009) | 22 | 0.1% | 21 | 0.7% | 21 | 0.75% | 11 | 0.39% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 22 | 0.1% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Rivoire (2018) | 22 | 0.1% | 18 | 0.6% | 18 | 0.64% | 18 | 0.63% |
Weimerskirch et al. (2009) | 22 | 0.1% | 16 | 0.53% | 16 | 0.57% | 14 | 0.49% |
Charrassin (2016) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Charrassin (2016) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Dewynter (2021) | 21 | 0.1% | 21 | 0.7% | 21 | 0.75% | 20 | 0.71% |
Hullé et al. (2003) | 21 | 0.1% | 19 | 0.63% | 19 | 0.68% | 16 | 0.56% |
Jarrett & Shirihai (2014) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Moutou (2016) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Thoisy & Bordin (2016) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Urtizberea (2016) | 21 | 0.1% | 20 | 0.66% | 20 | 0.71% | 11 | 0.39% |
Bell (1982) | 20 | 0.1% | 18 | 0.6% | 18 | 0.64% | 17 | 0.6% |
Proćków & Drábková (2023) | 20 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 20 | 0.1% | 20 | 0.66% | 20 | 0.71% | 19 | 0.67% |
Spitz et al. (2016) | 20 | 0.1% | 19 | 0.63% | 19 | 0.68% | 10 | 0.35% |
Courtecuisse (2006) | 19 | 0.09% | 14 | 0.46% | 14 | 0.5% | 13 | 0.46% |
Dulac (1867) | 19 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
Funk et al. (2007) | 19 | 0.09% | 10 | 0.33% | 10 | 0.36% | 7 | 0.25% |
Leraut (1997) | 19 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
Abraham (2022) | 18 | 0.09% | 16 | 0.53% | 16 | 0.57% | 16 | 0.56% |
Fourdrigniez & Meyer (2008) | 18 | 0.09% | 15 | 0.5% | 14 | 0.5% | 14 | 0.49% |
Linnaeus (1766) | 18 | 0.09% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Meurgey & Ramage (2020) | 18 | 0.09% | 18 | 0.6% | 18 | 0.64% | 18 | 0.63% |
Reverté et al. (2023) | 18 | 0.09% | 17 | 0.56% | 17 | 0.6% | 17 | 0.6% |
Rouy (1908) | 18 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1906) | 18 | 0.09% | 16 | 0.53% | 16 | 0.57% | 12 | 0.42% |
Uicn et al. (2015) | 18 | 0.09% | 15 | 0.5% | 15 | 0.53% | 14 | 0.49% |
Clements (2012) | 17 | 0.08% | 17 | 0.56% | 15 | 0.53% | 17 | 0.6% |
Linnaeus (1761) | 17 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Moench (1794) | 17 | 0.08% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Ramage (2017) | 17 | 0.08% | 17 | 0.56% | 17 | 0.6% | 17 | 0.6% |
Van Guelpen (2016) | 17 | 0.08% | 16 | 0.53% | 16 | 0.57% | 16 | 0.56% |
Flora of North America (1993-) | 16 | 0.08% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Goulletquer (2016) | 16 | 0.08% | 15 | 0.5% | 15 | 0.53% | 14 | 0.49% |
Horak & Mouchacca (1998) | 16 | 0.08% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Jourdan & Mille (2006) | 16 | 0.08% | 16 | 0.53% | 16 | 0.57% | 16 | 0.56% |
Mériguet & Zagatti (2016) | 16 | 0.08% | 16 | 0.53% | 16 | 0.57% | 12 | 0.42% |
Nyman (1882) | 16 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra et al. (2008) | 16 | 0.08% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Rafinesque Schmaltz (1810) | 16 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Speight (2013) | 16 | 0.08% | 15 | 0.5% | 15 | 0.53% | 15 | 0.53% |
Giard (1872) | 15 | 0.07% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Liimatainen et al. (2020) | 15 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Munzinger et al. (2016) | 15 | 0.07% | 9 | 0.3% | 9 | 0.32% | 8 | 0.28% |
Vaillant (2000) | 15 | 0.07% | 15 | 0.5% | 13 | 0.46% | 15 | 0.53% |
Deblock et al. (1960) | 14 | 0.07% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Fournier (1934-1940) | 14 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 14 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 14 | 0.07% | 14 | 0.46% | 14 | 0.5% | 14 | 0.49% |
Fricke et al. (2011) | 14 | 0.07% | 14 | 0.46% | 14 | 0.5% | 14 | 0.49% |
Host (1831) | 14 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 14 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Arcangeli (1882) | 13 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boom et al. (2011) | 13 | 0.06% | 13 | 0.43% | 13 | 0.46% | 12 | 0.42% |
Desbrosses & Etcheberry (1987) | 13 | 0.06% | 10 | 0.33% | 10 | 0.36% | 4 | 0.14% |
Lacoste (de) (2020) | 13 | 0.06% | 12 | 0.4% | 12 | 0.43% | 7 | 0.25% |
Meurgey (2011) | 13 | 0.06% | 12 | 0.4% | 12 | 0.43% | 12 | 0.42% |
Váňa et al. (2010) | 13 | 0.06% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Váňa et al. (2013) | 13 | 0.06% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Barau et al. (2005) | 12 | 0.06% | 11 | 0.36% | 11 | 0.39% | 10 | 0.35% |
Courtecuisse & Welti (2013) | 12 | 0.06% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Del Hoyo & Collar (2014) | 12 | 0.06% | 9 | 0.3% | 9 | 0.32% | 9 | 0.32% |
Fricke et al. (2009) | 12 | 0.06% | 11 | 0.36% | 11 | 0.39% | 11 | 0.39% |
Lafranchis (2014) | 12 | 0.06% | 11 | 0.36% | 11 | 0.39% | 10 | 0.35% |
Lafranchis (2016) | 12 | 0.06% | 11 | 0.36% | 11 | 0.39% | 10 | 0.35% |
Lamarck (1779) | 12 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebard & Speight (2019) | 12 | 0.06% | 12 | 0.4% | 12 | 0.43% | 12 | 0.42% |
Morat et al. (2012) | 12 | 0.06% | 9 | 0.3% | 9 | 0.32% | 8 | 0.28% |
Ochi (1972) | 12 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
O’Shea (2006) | 12 | 0.06% | 10 | 0.33% | 10 | 0.36% | 10 | 0.35% |
Schnakenbeck (1931) | 12 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Walbaum (1792) | 12 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Jamon (2010) | 12 | 0.06% | 11 | 0.36% | 11 | 0.39% | 11 | 0.39% |
Aulagnier et al. (2017) | 11 | 0.05% | 9 | 0.3% | 9 | 0.32% | 7 | 0.25% |
Basso (1999) | 11 | 0.05% | 11 | 0.36% | 11 | 0.39% | 11 | 0.39% |
Chapelin et al. (2012) | 11 | 0.05% | 10 | 0.33% | 10 | 0.36% | 9 | 0.32% |
Courtecuisse et al. (1996) | 11 | 0.05% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Cuvier & Valenciennes (1829) | 11 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1833) | 11 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 11 | 0.05% | 6 | 0.2% | 6 | 0.21% | 5 | 0.18% |
Molina et al. (2008) | 11 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Rageau (1958) | 11 | 0.05% | 11 | 0.36% | 11 | 0.39% | 11 | 0.39% |
Thouvenot & Bardat (2010) | 11 | 0.05% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Bay-nouailhat & Bay-nouailhat (2020) | 10 | 0.05% | 10 | 0.33% | 10 | 0.36% | 10 | 0.35% |
Bloch & Schneider (1801) | 10 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordin et al. (2021) | 10 | 0.05% | 10 | 0.33% | 10 | 0.36% | 4 | 0.14% |
Bourzat & Monie (1977) | 10 | 0.05% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Commission de l’Avifaune Française (2016) | 10 | 0.05% | 9 | 0.3% | 9 | 0.32% | 9 | 0.32% |
Döll (1843) | 10 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff (2021) | 10 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-Edwards (1841) | 10 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocamora (2004) | 10 | 0.05% | 9 | 0.3% | 8 | 0.28% | 9 | 0.32% |
Uicn et al. (2019) | 10 | 0.05% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Aptroot et al. (2011) | 9 | 0.04% | 7 | 0.23% | 7 | 0.25% | 6 | 0.21% |
Boisduval (1840) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Buyck (2013) | 9 | 0.04% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Catzeflis (2012) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 3 | 0.11% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 8 | 0.28% |
Denys et al. (2022) | 9 | 0.04% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Ephytia (2020) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 9 | 0.32% |
Gannier (2001) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 4 | 0.14% |
Gargominy et al. (1996) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 9 | 0.32% |
Garrigue (2007) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 4 | 0.14% |
G.E.M.M. (2012) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 4 | 0.14% |
Gmelin (1789) | 9 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jaouen et al. (2019) | 9 | 0.04% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Mitchill (1815) | 9 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Reinhardt (1837) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Séguy (1944) | 9 | 0.04% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Soubeyran et al. (2011) | 9 | 0.04% | 9 | 0.3% | 9 | 0.32% | 8 | 0.28% |
Van Dijk et al. (2012) | 9 | 0.04% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
CHN (2017) | 8 | 0.04% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Dauvin et al. (2003) | 8 | 0.04% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Dekay (1842) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1892) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel et al. (2005) | 8 | 0.04% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Fourcroy (1785) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Guth (1971) | 8 | 0.04% | 7 | 0.23% | 7 | 0.25% | 6 | 0.21% |
Jourdan (2020) | 8 | 0.04% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Lacepède (1803) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1778) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1913) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Savulescu (1952) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Schur (1866) | 8 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennikov & Kurtto (2017) | 8 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Siu et al. (2017) | 8 | 0.04% | 8 | 0.26% | 8 | 0.28% | 8 | 0.28% |
Alonso et al. (2016) | 7 | 0.03% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Anonyme (2014) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 5 | 0.18% |
Audinet-Serville (1823) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beker et al. (2016) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boreau (1857) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bricaud (2007) | 7 | 0.03% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Candolle (1815) | 7 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dekay (1842) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewarumez et al. (2011) | 7 | 0.03% | 6 | 0.2% | 5 | 0.18% | 6 | 0.21% |
Dewynter et al. (2021) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 5 | 0.18% |
Dickinson & Remsen (2013) | 7 | 0.03% | 7 | 0.23% | 4 | 0.14% | 7 | 0.25% |
Duss (1903) | 7 | 0.03% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Frenot et al. (2005) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Furminieux (2019) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Gandoger (1884) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillermet (2004) | 7 | 0.03% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Koch (1837) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 7 | 0.03% | 6 | 0.2% | 6 | 0.21% | 5 | 0.18% |
Meurgey & Picard (2011) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Miller (1768) | 7 | 0.03% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Müller (1776) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolet (1847) | 7 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ochyra & Suárez (2011) | 7 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Pallas [1814] | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontoppidan (1763) | 7 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Preynat (2013) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 7 | 0.25% |
Risso (1810) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 7 | 0.03% | 7 | 0.23% | 7 | 0.25% | 6 | 0.21% |
Vitt & Marsh (1988) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaremski et al. (2014) | 7 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Aublet (1775) | 6 | 0.03% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Bonnier & Layens (1894) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambecèdes et al. (2012) | 6 | 0.03% | 5 | 0.17% | 5 | 0.18% | 4 | 0.14% |
Candolle (1852) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Charbonnel (1990) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Christensen & Heilmann-clausen (2013) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Collette & Nauen (1983) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Cuvier (1829) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1902) | 6 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duméril (1870) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 6 | 0.03% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
Fleming (1828) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 6 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gonzalez et al. (2009) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
González‐Elizondo & Peterson (1997) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Goode & Bean (1896) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedenäs (1997) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Ifremer (2009) | 6 | 0.03% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Jouveau et al. (2018) | 6 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Karadjian et al. (2022) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Kryvomaz et al. (2019) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Kuntze (1891) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 6 | 0.03% | 5 | 0.17% | 5 | 0.18% | 3 | 0.11% |
Lorvelec et al. (2007) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 6 | 0.21% |
Mikkola & Honey (1993) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nardo (1827) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2014) | 6 | 0.03% | 6 | 0.2% | 5 | 0.18% | 6 | 0.21% |
Roux (2013) | 6 | 0.03% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Rouy (1909) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1905) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 4 | 0.14% |
Schlesak et al. (2018) | 6 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Schuster (1969) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Shirihai (2003) | 6 | 0.03% | 6 | 0.2% | 6 | 0.21% | 2 | 0.07% |
Thibaud (2017) | 6 | 0.03% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Turcati (2019) | 6 | 0.03% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Adelski (2012) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Bocquet (1953) | 5 | 0.02% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Bonfils (1969) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Bubani & Penzig (1900) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Camiñas et al. (2021) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Cardot (1916) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevin & Savina (2013) | 5 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Coutanceau (2006) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Crum & Anderson (1981) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrhardt (1971) | 5 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Fabricius (1775) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1781) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Falkner et al. (2002) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Flatberg (1983) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fourreau (1868) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (2011) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Godart & Duponchel (1834) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Ilkiu-Borges (2015) | 5 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Greuter & Troia (2015) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gutierrez (1981) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Honey & Scoble (2001) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindberg (1958) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Linnaeus (1767) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mennema (1989) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Moench (1794) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Henle (1841) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2004) | 5 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Øvstedal (2010) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Peck et al. (2014) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Peck (2011) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Perrin et al. (2002) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 1 | 0.04% |
Persoon (1805) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Reschke et al. (2022) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 5 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Roalson et al. (2010) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Robineau & Duhamel (2006) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 2 | 0.07% |
Robineau (2005) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 1 | 0.04% |
Samaran & Guinet (2009) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 2 | 0.07% |
Scopoli (1771) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Theuerkauf et al. (2010) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Tostain (1980) | 5 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Váňa et al. (2012) | 5 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Vidal (2012) | 5 | 0.02% | 5 | 0.17% | 5 | 0.18% | 5 | 0.18% |
Young (1970) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zelhuber (2009) | 5 | 0.02% | 5 | 0.17% | 4 | 0.14% | 4 | 0.14% |
Abraham (2017) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Allain & Morice (1971) | 4 | 0.02% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Ausilio & Zotier (1989) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Barré (2021) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Barrioz & Morinière (2007) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Boer et al. (1999) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 2 | 0.07% |
Boer (2000) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 1 | 0.04% |
Boisduval (1832-[1835]) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bonnaterre (1788) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon-Navaro et al. (2005) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Bour et al. (2008) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Boyer & Rivault (2003) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Brassard et al. (1989) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Breton et al. (2003) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Brünnich (1764) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1824) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Casale et al. (2021) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Catalán et al. (2012) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clements et al. (2015) | 4 | 0.02% | 3 | 0.1% | 2 | 0.07% | 2 | 0.07% |
Coiffait (1956) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif & Bebest (2019) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Corriol & Hannoire (2018) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Dejean (1829) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Del Hoyo & Collar (2016) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Wynne (2016) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 3 | 0.11% |
Denux & Zagatti (2010) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Dijkstra et al. (2015) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Doucet (2016) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Duguy (1988) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Duguy (1994) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Duguy (1997) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Dulau-Drouot et al. (2008) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 3 | 0.11% |
Evenhuis (2018) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Fedosov et al. (2021) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Flora of North America Editorial Committee (2007) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Fourriére et al. (2014) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Fretey & Triplet (2022) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Gandoger (1875) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1876) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier (2002) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 3 | 0.11% |
Gannier (2009) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 2 | 0.07% |
Geoffroy (1762) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Giard (1879) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gill (1883) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1788) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy (2000) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Grand & Boudot (2007) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Grand et al. (2014) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Grenier & Godron (1850) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hébrard (1970) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heidemann & Seidenbusch (2002) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Hekking & Sipman (1988) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Heppner (1982) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jay et al. (2009) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jordan (1864) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kerney & Cameron (1999) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Lacepède (1801) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lamarck (1779) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2012) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Malm (1877) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré & Rochat (2008) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Massary et al. (2019) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Morinière & Dell'amico (2011) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Muller et al. (2012) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Muratet (2015) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Nakamura (1985) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Panzer ([1796]) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prelli & Boudrie (2021) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prévost & Mougin (1970) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 3 | 0.11% |
Rafinesque (1810) | 4 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Rageau (1959) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Reichenbach (1830-1832) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Richter (1890) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivoire (2013) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Roux et al. (2006) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Rouy (1899) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1912) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1997) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Storer (1839) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain & Dujardin (1988) | 4 | 0.02% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Vaillant & Brunhes (1981) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Vayssières et al. (2001) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Vidal & Vansteene (2021) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Vieillot (1807) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Vieillot (1819) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1863) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Welter-schultes (2012) | 4 | 0.02% | 4 | 0.13% | 4 | 0.14% | 4 | 0.14% |
Anonyme (2023) | 3 | 0.01% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Arnold & Ovenden (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Bartoli (1972) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bedot (1910) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bertrand & Roux (2018) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Binaghi (1942) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bioinsight/diren & Guyane (2006) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Birdlife International (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Blainville (1816) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Blank & Taeger (1998) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Blat (2013) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Bloch & Schneider (1801) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Boddaert & Daubenton (1783) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Borgato et al. (2020) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Borsa (1997) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 1 | 0.04% |
Bousquet (2016) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Breitling et al. (2016) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunet et al. (2017) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1902) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Burneleau (1983) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Campbell (1976) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Caparrós et al. (2016) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Cariot & Saint-lager (1889) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Chartois et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Chatton & Brément (1909) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chevalier (2006) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Chown & Convey (2016) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Ciccione et al. (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Clarke (1971) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Clauzade & Roux (1985) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1974) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Couté & Garrouste (2009) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Crillon & Cuzange (2020) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Crum & Anderson (1981) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Davies, L. & Greene, S.W. (1976) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Dejean (1831) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2016) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Deméré (2014) | 3 | 0.01% | 3 | 0.1% | 0 | 0% | 3 | 0.11% |
Dewynter et al. (2019) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Dewynter et al. (2019) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Dewynter et al. (2022) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Dewynter et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Dewynter et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Diaz & Cuzange (2009) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 1 | 0.04% |
Don (1834) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Dubois et al. (2008) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duffaut et al. (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (1998) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (1999) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (2000) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (2002) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (2006) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy et al. (2007) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy (1990) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Duguy (1996) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Entraygues (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Esper & Charpentier (1789-[1804]) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Étaix-bonnin et al. (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Fabricius (1787) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Facciolà (1882) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fedosov et al. (2023) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Florence (2004) | 3 | 0.01% | 3 | 0.1% | 2 | 0.07% | 2 | 0.07% |
Fourcroy (1785) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gadeau de Kerville (1900) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gannier (2000) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 1 | 0.04% |
Garrison (1984) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Garrouste & Hervé (2009) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Geer (1774) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Genard & Lescourret (1987) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Gill (1995) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Gilot et al. (1992) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Girondot (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Grand et al. (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Greipsson & Priest (1983) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Godron (1856) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle (2002) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hammond (1972) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Hartig (1840) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassler & Schmitt (2018) | 3 | 0.01% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Haworth (1803-1828) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1916) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hoff & Daszkiewicz (2001) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Hullé & Vernon (2021) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Imshaug (2019) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Ingels et al. (2003) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Acanthoscelides obtectus sur des plantes de Phaseolus vulgaris en plein champ. Bulletin de la Société Zoologique de France, 110: 395-402.">Jarry et al. (1985) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Jolinon (1985) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Jordan & Fourreau (1868) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Joshi et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Kawamura (1994) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 0 | 0% |
Kienberger et al. (2016) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kiszka et al.(2007) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Knoepffler et al. (1990) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Koehler (1921) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kylin et al. (2012) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Larson (1989) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Le Peletier (1823) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Scao et al. (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Leach (1818) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2014) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1818) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Link (1821) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohez (2013) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Mammola & Milano (2019) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Marsham (1802) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2017) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Massary et al. (2018) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Massary et al. (2020) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Massary et al. (2021) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Mcdevit & Saunders (2017) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Méheust et al. (2018) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Meigen (1822) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Millière (1881) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau et al. (2015) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Müller (1774) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
N'Yeurt & Payri (2007) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Oberthür (1910) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra & Stebel (2008) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Pallas (1770) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1776) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1998) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Payri (2007) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Pearman et al. (2020) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Persoon (1807) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ponge et al. (2003) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Poulain et al. (2011) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Probst et al. (2022) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Probst (2001) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Questel et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Questel et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Questel (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Read & Farman (2018) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Read et al. (2023) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Remillet (1988) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Renauld & Cardot (1889) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodríguez-Prieto et al. (1999) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Roemer & Schultes (1819) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi-santos et al. (2007) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 1 | 0.04% |
Rouy & Camus (1901) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1903) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 2 | 0.07% |
Salazar-Vallejo (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Sauvignet et al. (2000) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Schrank (1781) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster et al. (2015) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Sherborn & Woodward (1901) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Stenseth (1980) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Stierlin (1861) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2014) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Thouvenot et al. (2011) | 3 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Thunberg & Borgström (1784) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier (1980) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Urtizberea (2021) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 0 | 0% |
Verity (1927) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Villers (1789) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Voisin et al. (2017) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Vroman (1968) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wigginton (2009) | 3 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Young (1971) | 3 | 0.01% | 3 | 0.1% | 3 | 0.11% | 3 | 0.11% |
Zika & Tucker (2017) | 3 | 0.01% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
AAMP (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Adamonyte et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Ah-Peng (2007) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ainley et al. (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Alonso-zarazaga & Evenhuis (2017) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Arup et al. (2013) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Ascanius (1772) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascanius (1775) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ascherson & Graebner (1897) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Atton (1990) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Aubouin et al. (2016) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Azam (1893) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bacchet et al. (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Baldi et al. (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Baral et al. (2014) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Barbut & Voisin (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Barbut et al. (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bauer & Sadlier (2000) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Beauchamp (1914) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Beaucournu et al. (1998) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bednarek-ochyra et al. (2015) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry & Smith-Vaniz (1978) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bertin (1928) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bertrand (1949) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand (1950) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Beuret (1934) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Blainville (1810) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanc (1909) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1795) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Bobrov et al. (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bochaton et al. (2021) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Boisduval & Lacordaire (1835) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bon (1999) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet et al. (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bourcier (1988) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bourmaud (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brehm (1831) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Breitling et al. (2015) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Brotherus (1906) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1788) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bush (1905) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Butaud (2021) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Camino et al. (2008) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Carine et al. (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Carine et al. (2004) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Carpenter & Glare (2010) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Casevitz-Weulersse & Galkowski (2009) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Catzeflis (2018) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cépède (1814) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Céréghino & Lavandier (1997) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Chaix (1785) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Chappuis et al. (1974) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Chartier et al. (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Chassard-Bouchaud et al. (1985) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cheesman (1927) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Chevallier et al. (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cicero & Johnson (1998) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Claparède (1863) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Clerck (1757) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Clerck (1759) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1875) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Combescot-Lang (1976) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Combrisson (1999) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Coombs & Woodroffe (1973) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Costa (1829-1853) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1838) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1877) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1877) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1877) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot & Rabaute (2016) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Courtecuisse et al. (2018) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Couteyen & Papazian (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Crantz (1766) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cuvier & Valenciennes ([1832]) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1847) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1848) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
dal Molin (2009) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Daly et al. (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Daniel et al. (2020) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Daniels & Eddy (1985) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin et al. (1991) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Davant (1967) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Davis & Davis (2009) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Debout (2001) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delcroix et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delfosse & Dubois (2018) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delfosse (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delfosse (2017) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delfosse (2024) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Delsalle & Sechet (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Denis (1921) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Derkarabetian et al. (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Deshayes (1863) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter & Claessens (2020) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Dewynter et al. (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Dilman (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Donovan (1803-08) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1816) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Doucet (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Douyer (1981) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Drapikowska et al. (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dubief & Gallais (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy et al. (1997) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy et al. (2003) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy et al. (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy (1986) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy (1987) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy (1992) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy (1993) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duguy (1995) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Elven & Murray (2008) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Černý et al. (2020) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Esper ([1796-1805]) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (1989) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Faber (1829) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fauvel (1904) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldberg et al. (2010) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ferlay et al. (2023) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fiori (1925) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossen et al. (2016) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Frahm (2010) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fujii et al. (2019) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gallien (2008) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gargominy (2011-2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Garman (1913) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gentry et al. (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Germar & Kaulfuss (1817) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gibson & Baker (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gill & Thiele (1997) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Girondo (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Goeze (1783) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1956) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gomy et al. (2016) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Goode & Bean (1895) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Grand et al. (2019) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Greene & Greene (1963) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Große-veldmann (2017) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Guenée ([1858]) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Guermeur (1987) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gunnerus (1765) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gunnerus (1765) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1767) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Handfield & Handfield (2021) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Hauk et al. (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hausmann & Viidalepp (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Héros et al. (2007) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hill (1768) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway & Peters (1976) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Horstmann (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Houard (2020) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Howell Rivero (1936) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner ([1790-1833]) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1793) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Husnot (1908) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyvönen (2006) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-mer (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Iperti & Bertand (2001) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
IUCN (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
James (1875) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1862) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jordan (1896) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Joubert & Margerit (1986) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Julien (1881) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jung et al. (2024) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Karsholt et al. (2006) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kasamatsu & Joyce (1995) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kasamatsu et al. (2000) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Katsoyannos et al. (1997) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Keith et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kieffer (1898) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiesenwetter (1851) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kilgallen & Lowry (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kirby (1890) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner (1990) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner (2002) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2010) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Klimaszewski et al. (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kock et al. (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Köckinger & Hedenäs (2017) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Koechlin (1977) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Kulbicki (comm. pers., 2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Labitte (1955) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Laforgue (2015) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Lagourgue et al. (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lam et al. (2024) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lamy & Pointier (2018) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lansdown (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Laporte de Castelnau & Brullé (1840) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Laran et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lauriaut et al. (2021) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Leach (1815-1875) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Leaper et al. (2008) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lebas et al. (2016) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Leboulenger (1989) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Legrand (1949) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Legrand (1950) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Legrand (1953) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lemée (1953) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lemée (1955) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lepechin (1769) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2005) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lesueur (1818) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1821) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Léveillé (1917) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Clergeau (2002) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Levesque & Delcroix (2016) | 2 | 0.01% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Levring (1944) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Linnaeus (1759) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Linnaeus (1767) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2006) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Madill & Hovingh (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Majka & Langor (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Malloch (1933) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Martinet et al. (1765) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Massé (1982) | 2 | 0.01% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Mathews (1914) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Matsuoka et al. (2005) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Mays et al. (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
McNair & Cramer-Burke (2006) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mctavish (2002) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Meganck et al. (2017) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Merrem (1820) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer (1819) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1878) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Millot et al. (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Miranda et al. (2009) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Montagu (1808) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Monteiro et al. (2020) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Moreau (1881) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Muñoz (2005) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nel et al. (2020) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolet (1842) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nilsson (1832) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nordmann (1840-1842) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
N'Yeurt & Payri (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Ochi (1982) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochs (1949) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Osório (1909) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Palko et al. (1982) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pallas (1766) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1797]) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. 2006 | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pascal et al. (2006) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Paul & Lefranc (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Payri & N'yeurt (1997) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Perez Canto (1886) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Peron (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Peterson et al. (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pezy et al. (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Philippi (1887) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierre & Lalanne-Cassou | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pimentel & Sahuquillo (2008) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Plášek et al. (2015) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Poisson (1999) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pons et al. (2005) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Potin (2013) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Poupin et al. (1999) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Probst (1997) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Probst (1997) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Probst (1998) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pteridophyte Phylogeny Group (2016) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Questel (2016) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Questel (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Rambur (1829) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Jean (2021) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Redon & Chorein (2009) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Reinhardt (1825) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Renauld & Cardot (1888) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Reveal et al. (1991) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Revel et al. (2024) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Rhodin et al. (2017) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Richard et al. (1982) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Riina et al. (2013) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Risso (1816) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (1989) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Robineau (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Robineau-Desvoidy (1841) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rognes & Blackith (1990) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Rönkä et al. (2016) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ronot (2007) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Rossi (1792) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rottemburg (1775) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux et al. (2022) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sabine (1819) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sahlberg (1871) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint et al. (1978) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Say (1825) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schattanek-Wiesmair et al. (2024) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Schauberger (1934) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt (1875) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuler (1964) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennen & Frère (1936) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sentz‐Braconnot (1966) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Séret & Quod (2023) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Shaw & Nodder (1792-1793) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Shinonaga et al. (1991) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Silva et al. (1996) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Simon (1916) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1849) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1910) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Snodgrass & Heller (1905) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Société et al. (1969) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström et al. (2016) | 2 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
Spitz et al. (2015) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 0 | 0% |
Sprengel (1825) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Sprengel (1826) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Srot (1979) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Stefanovic et al. (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Steudel (1841) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Stewart (1934) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Stewart (1934) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Stewart (2014) | 2 | 0.01% | 2 | 0.07% | 0 | 0% | 2 | 0.07% |
Storer (1858) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler & Crandall-Stotler (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Suárez & Schiavone (2011) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Suberbielle et al. (2020) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Swainson (1839) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck & Schlegel (1850) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Theodorides (1955) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Thiele et al. (1999) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Thiele et al. (2004) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Thomas (1991) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Thomas (2015) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Thompson (1938) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Thunberg (1787) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Toll (1985) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2006) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Tunstall (1880) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Turton (1932) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Váňa & Long (2011) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2014) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Valenciennes (1836-1844) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Canneytet al. (2008) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Van Der Putten et al. (2010) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 1 | 0.04% |
Vane-Wright & De Jong (2003) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Vasselon et al. (2019) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Vénec-Peyré (1985) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal & Delfosse (2012) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Vidal (2019) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Vieillot (1819) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Viette (1950) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Villars (1786) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Villastrigo et al. (2017) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Villeneuve (1918) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Walters (1953) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1939) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (1813) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wilson (1814) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Winkler et al. (2009) | 2 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Yarrell (1829) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrell (1832) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Zahradník & Poussereau (2022) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Zardi et al. (2011) | 2 | 0.01% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Abbayes (1931) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Abhaya & Probst (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Abril et al. (1986) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Acevedo-Rodríguez & Strong (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Adler (2020) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ah-Peng et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Akhani et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Allioni (1785) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Andouche et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Andrew et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Andrieux et al. (1981) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anisimova & Cochrane (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2002) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Anonyme (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Archaux & Chatard (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Armada (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Arnaud (1974) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Arts (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ascherson & Graebner (1910) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubert & Beaucournu (1976) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Aubert de la Rüe (1932) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Audige (1927) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Augener (1918) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ayres (1848) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Badré & Deschâtres (1979) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagnall (1939) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Baird (1858) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bakalin et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bakalin (2001) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bakalin (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bakker & Noordeloos (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bal (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Baldi et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Balfour-Browne (1944) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Baraniak (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbancey (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Barbancey (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bardat et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Barker et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré & Géraux (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Barthélémy (1926) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartoli (1974) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Baylac (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bayón (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu et al. (1985) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Beaucournu et al. (1992) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Beaucournu (1968) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaufils & Lecocq (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Beaufils (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Beauvieux et al. (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bellan-Santini & Ledoyer (1974) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bellan-Santini (1972) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bellan-Santini (1972) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bellmann (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bencheton et al. (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bénito-espinal (1990) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Berce (1867) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bertault (1988) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Berton (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bertrand (1949) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Bichain et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bidaud et al. (2009) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bidaud et al. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (1862) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Birdlife International (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Birdlife International (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Birdlife International (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Birdlife International (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blainville (1810) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchot (1992) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blatchley (1910) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1782-1784) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1784) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1787) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1788) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blockeel et al. (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blockeel et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blockeel et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Blom (1996) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bocher et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bocquet & Stock (1958) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boggan et al. (1997) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boidin & Gilles (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boie (1835) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisduval (1833) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boisseau & Lubet (1955) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boissel & Urtizberea (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bonaparte (1837) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1838) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bonaparte (1839[1838]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnefoy & Marchal (1942) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boreau (1849) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Boschert & Dronneau (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Botrel et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boubert et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bouchon-Navaro & Louis (1986) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bouget et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Boullet et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bourgade (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bourgade (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bouxin & Legendre (1952) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Branch (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Brattey et al. (1990) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Braun-blanquet (1933) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1822) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brewster (1895) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brewster (1902) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jornal de Sciencias Mathematicas, Physicas e Naturaes, Academia Real das Sciencias de Lisboa 2(7): 233-238.">Brito Capello (1869) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1929) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (1940) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brugel (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brugneaux & Pérès (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Bruguière (1789-1792) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun (1958) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brunhes (1979) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Brünnich (1768) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Budylenko (1977) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Calenge et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Campana-rouget & Biocca (1955) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Candolle (1830) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1838-1839) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1848) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1864-1868) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Candy et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Canu (1891) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Casey (1884) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Casey (1896) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Catil (2013) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cerchio et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Chaine & Duvergier (1928) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chainey (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chambault et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chambers (1875) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Champagne et al. (1997) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Champion (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chandler (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chassaing et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chastel et al. (1981) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chastel et al. (1987) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chastel et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chatton & Lwoff (1930) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chatton & Séguéla (1936) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chauvel et al. (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chavoutier (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chebbah et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cheek (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheke (1987) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chesser et al. (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevallier et al. (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chevreux & de Guerne (1893) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1887) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1908) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Chopard (1924) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Christenhusz (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ciavatti et al. (1993) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ciccione (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ciccione (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
CJBN (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Clark & Harrison (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Clemens (1861) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Clemens (1865) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Clements (1992) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau & Lorvelec (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau & Pascal (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau & Vigne (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau & Vigne (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau et al. (2003) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Clergeau et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Clergeau et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Coatmeur (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cocco (1832) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochereau (1966) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Coiffait (1976) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Colindre (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Collectif (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Colligros & Lebecque (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Collinge (1917) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Comfort (1938) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Contejean (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Contejean (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cornish (1885) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Correa & Silva (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Corti (1914) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (1862) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Coste & Ricard (1990) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Coste et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Coste (1937) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Costea et al. (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Costrel & Corainville (1929) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cotte et al. (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Couch (1849) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Couch (1866) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1861) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Coughlan et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Coulon et al. (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Counihan et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Couteyen (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cowie (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Crantz (1766) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Creau (1996) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Creighton (1950) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1997) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cresson (1865) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Crochet et al. (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Crop et al. (2013) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Crop et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Croset et al. (1980) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Crouzier (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Csabaï (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Cunha et al. (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1792) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dachy (1979) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Dadant & Etienne (1973) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dall et al. (1938) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalleau et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Damgaard & Zettel (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Danjon (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Danois (1913) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Dauvin et al. (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Davis & Davis (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Davoult et al. (1999) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Davoult (1990) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
De Geer (1773) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
De Haan & Moreau (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
De Sloover (1986) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Debenay & Cabioch (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Debenay (2013) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock (1966) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Deboulonne (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Debout (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dechelle & Ingels (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Deflandre (1960) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Deflandre (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Deflandre (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Déjan (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Déjean et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dejean (1825) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delacour (1963) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delbol & Perez (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delcroix et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delfosse & Iorio (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delfosse & Iorio (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delfosse & Tillier (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delfosse (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delhaes et al. (2001) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delnatte & Meyer (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Delpont (2019) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Delrieu-Trottin et al. (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Den et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dentinger et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Des et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Desbrosses (1934) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Desbrosses (1935) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Desplanques & Hébrard (1972) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Desportes (1838) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Desse-berset & Williot (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Desse-Berset & Williot (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Desse-Berset (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Devaud & Lebouvier (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dickinson & Christidis (2014) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dollfus (1960) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dollfus (1966) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1832) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Doubleday (1847) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Doubleday (1850) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreff & Delliere (1994) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury ([1770-1773]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury (1773) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Düben et al. (1844) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Cugnasse (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dubois & Louvet (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dubois et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dubois (1996) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dubois (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duftschmid (1812) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguy & Duron (1981) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy & Duron (1982) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy & Duron (1983) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy & Duron (1984) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy & Duron (1985) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy et al. (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy et al. (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy (1983) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy (1988) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duguy (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Dulac (1883) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-martial et al. (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duponchel (1838-[1840]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Duponchel (1842-[1845]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Duquef (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Eaton et al. (1879) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Eaton (1922) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Edward et al. (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Edwards (1913) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Efe et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ehrhart (1780) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ekrt et al. (2022) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ellis et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ellis et al. (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ellis et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ellis et al. (2020) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
Emilie et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Eppo (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Eppo (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ersts & Rosenbaum (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Ertz & Diederich (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Erxleben (1777) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Esmark (1866) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Esper & Charpentier (1795-[1806]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Etcheberry (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Etienne & Vilardebó (1978) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Evenhuis (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Evenhuis (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Eyton (1838) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fabricius ([1777]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1779) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1780) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Facciolà (1882) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fadda (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fall (1923) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fall (1924) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fallén (1817) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fauvel (1867) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fauvel (1903) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fawcett & Smith (2021) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
Felber-girard et al. (1996) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ferrand et al. (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fischer (1925) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fitch (1856) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleischmann & Gonella (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fleming & Jackson (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Flora iberica | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Foote et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Forel (1902) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1946) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Forskål (1775) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fort & Barrière (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fougère et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fournier (1928) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1908) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Francoeur (1977) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fremont (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fretey & Bour (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fretey et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fretey (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Fretey (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Frétey (2022) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Frisvoll (1983) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Frölich (1828) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuchs (1974) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gadeau de Kerville (1894) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaertner (1791) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gall et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Galli (2006) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Galliard (1934) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gallien (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Garman (1880) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaudin (1828) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gebler (1830) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérard et al. (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gerber (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gerhard ([1850-1853]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Germar (1821) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1824) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gernigon & Lacaze (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gernigon (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ghiliani (1852) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Ryder (1883) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gill (1861) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1864) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1873-1874) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1878) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (1997) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Girard (1855) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gistel (1848) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Giudicelli (1964) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gmelin (1790) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Godart (1822) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
González-Miguéns et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Goode & Bean (1877) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1879) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Goode & Bean (1883) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Goode (1881) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren & Galil (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulson & Wright (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Graber & Euzeby (1976) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Hekking (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gravier-Bonnet (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Gray (1846) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier (1950) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Greuter & Raus (2002) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffiths & Florens (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Grisebach (1866) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle & Onraedt (1974) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Grote (1873) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Zones humides infos, n°64-65, 32 pp.">Groupe d'experts "Zones humides" (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Guegan (1970) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Guenée (1852) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Guilcher et al. (1965) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Guinet (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Günther (1864) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1866) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1878) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1888) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Günther (1889) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gussone (1827) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gussone (1843) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gyllenhal (1827) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hafellner & Türk (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hamard et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Hammes & Putoa (1986) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Harris (1850) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Harris (1941) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartig (1837) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1820) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassemer et al. (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hebard (1933) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hébrard (1984) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedenäs (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hemming (1933) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hemsley (1885) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hennique et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hentschel et al. (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hentschel (1914) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Heppner (1981) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbst (1783) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Herdman (1882) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Herzberg (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hinton (1941) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hipeau-Jacquotte & Coste (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hoffmann & Smith (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Hoffmann (1796) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1804) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1977) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Holub (1969) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Holyoak & Pedersen (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Holyoak (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Homeyer (1853) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hübner (1796-[1836]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1816-[1826]) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Huemer et al. (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1766) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hufnagel (1767) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugonnot & Celle (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hugonnot & Chavoutier (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Hynes (1959) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
ICZN (1954) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ignatov & Milyutina (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ignatov et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Imler (1938) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Isaac (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Isenmann et al. (1971) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ito et al. (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
IUCN (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
IUCN (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Izri & Akhoundi (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jackson (1938) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jackson (1941) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jackson (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Janda & Abbott (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jansson (1982) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jaquemet et al. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Jargeat et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jargeat et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jeannel & Jarrige (1949) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeannel (1941) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jefferson & & Van Waerebeek (2002) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jehl et al. (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jensen (1905) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Joannis (1909) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Joannis (1915) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson & Wolman (1984) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Johnson (1901) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1973) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Evermann (1898) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jordan & Gilbert (1881) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1892) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouan (1863) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jourdain et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Jourdan et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Joyeux & Baer (1955) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Joyeux (1923) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Judkins & Kensley (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Karaa et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Karsch (1853) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kasamatsu et al. (1995) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Kasamatsu et al. (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Kassebeer (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kassebeer (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kearfott (1907) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Dorson (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Keith & Machino (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Keith et al. (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Keith et al. (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Keith (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kieffer (1913) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilburn (1973) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirby (1802) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kiszka et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Klug (1816) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Knapp (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Koch (1844) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1845) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kolenati (1846) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kondratyuk et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Konstantinova & Vasiljev (1994) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kraepelin (1896) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1845) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1845) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1852-53) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1855) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kugler (1967) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Kuhl (1820) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kummer (1871) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
Kurahashi & Fauran (1980) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Labat (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lacomme (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lacourt (1985) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lafresnaye (1848) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lagarde (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lage-Yusty et al. (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lamarck & Candolle (1805) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1786) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1801) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamb (1977) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (1988) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lamy (1978) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lang & Lecocq (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lansdown & Jarvis (2004) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeyrouse (1813) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Laran et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Latham (1787) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1790) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1810) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1973) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société Zoologique de France, 38: 282-288, 304-315.">Le Danois (1913) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Maitre & Chadee (1983) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Léotard & Chaline (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Leaper et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Lechapt (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lécuru & Courtecuisse (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Ledebour (1851) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lefranc & Issa (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Legendre (1923) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Leistikow & Wägele (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lejeune & Courtois (1831) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemoine & Quindroit (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lent & Wygodzinsky (1945) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1975) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lesage et al. (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lescure et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lesson (1828) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Lesson (1831) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lethierry (1881) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lethuillier (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Letournel et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Letournel et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Levesque (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Liardet & d'Auzon (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Liardet (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lichtenstein (1823) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lieftinck (1966) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lieftinck (1975) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lienig & Zeller (1846) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société d'Histoire Naturelle des Ardennes, 97: 67-69.">Ligeron (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Link (1829) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1762) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Löbl & Smetana (2013) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Loisier et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Loison (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lorvelec & Clergeau (2003) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Pascal (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lorvelec & Vigne (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lorvelec & Vigne (2003) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lorvelec et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lou & Koponen (1986) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Louette & Cousin (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Louisin & Probst (1996) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Loury & Puissauve (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lovén (1845) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lowe (1838) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Lütken (1887) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lütken (1892) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddalena & Zuffa (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mady et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Magaud & D'aubusson (1906) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Maillard (1978) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Maillard (1998) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Majka & Langor (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Malloch (1932) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Malm (1861) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mandák et al. (2005) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
Manns & Anderberg (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marchand (1980) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Marcos-garcía et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marié et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Marinov et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marinov et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marinov et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marion & Clergeau (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Marion & Marion (1982) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Marion (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marion (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marion (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Marshall (1955) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
Martin et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Martin-sans (1933) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Martiré (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Marx et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mary (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mas-Coma et al. (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Massé (1982) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mathias & Fournal (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Mayr (1861) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Medetian & Miaud (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
Meigen (1830) |