Espèces protégées au niveau national
3945 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Uicn et al. (2017) | 1156 | 10.46% | 1102 | 36.41% | 945 | 39.42% | 898 | 34.55% |
| Tison et al. (2014) | 1009 | 9.13% | 500 | 16.52% | 443 | 18.48% | 438 | 16.85% |
| Remsen et al. (2013) | 596 | 5.39% | 563 | 18.6% | 563 | 23.49% | 439 | 16.89% |
| Linnaeus (1758) | 390 | 3.53% | 93 | 3.07% | 90 | 3.75% | 66 | 2.54% |
| Rinaldi (2016) | 276 | 2.5% | 260 | 8.59% | 260 | 10.85% | 192 | 7.39% |
| Hoff & Daszkiewicz (2001) | 222 | 2.01% | 141 | 4.66% | 113 | 4.71% | 102 | 3.92% |
| Uicn et al. (2015) | 210 | 1.9% | 199 | 6.57% | 192 | 8.01% | 154 | 5.93% |
| Estrade et al. (2016) | 207 | 1.87% | 195 | 6.44% | 195 | 8.14% | 144 | 5.54% |
| Carzon et al. (2016) | 205 | 1.85% | 193 | 6.38% | 193 | 8.05% | 142 | 5.46% |
| Mertens & Wermuth (1960) | 177 | 1.6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure et al. (2012) | 170 | 1.54% | 117 | 3.87% | 70 | 2.92% | 87 | 3.35% |
| Levesque & Delcroix (2018) | 168 | 1.52% | 164 | 5.42% | 146 | 6.09% | 147 | 5.66% |
| Questel (2020) | 134 | 1.21% | 130 | 4.29% | 114 | 4.76% | 112 | 4.31% |
| UICN Comité français, OFB & MNHN (2021) | 129 | 1.17% | 129 | 4.26% | 129 | 5.38% | 98 | 3.77% |
| Questel & Le Quellec (2012) | 115 | 1.04% | 109 | 3.6% | 102 | 4.26% | 87 | 3.35% |
| Lescure et al. (2022) | 111 | 1% | 109 | 3.6% | 109 | 4.55% | 109 | 4.19% |
| Clements (2012) | 109 | 0.99% | 97 | 3.2% | 80 | 3.34% | 80 | 3.08% |
| Yokoyama (2013) | 109 | 0.99% | 98 | 3.24% | 93 | 3.88% | 71 | 2.73% |
| Arnold & Ovenden (2014) | 100 | 0.9% | 62 | 2.05% | 62 | 2.59% | 34 | 1.31% |
| Lescure & Marty (2000) | 100 | 0.9% | 44 | 1.45% | 44 | 1.84% | 44 | 1.69% |
| Aulagnier (2009) | 94 | 0.85% | 89 | 2.94% | 89 | 3.71% | 61 | 2.35% |
| Henderson & Breuil (2012) | 93 | 0.84% | 51 | 1.68% | 42 | 1.75% | 41 | 1.58% |
| Tostain et al. (2013) | 90 | 0.81% | 76 | 2.51% | 74 | 3.09% | 59 | 2.27% |
| Gargominy et al. (2011) | 85 | 0.77% | 71 | 2.35% | 52 | 2.17% | 63 | 2.42% |
| Gmelin (1789) | 84 | 0.76% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Falkner et al. (2002) | 81 | 0.73% | 58 | 1.92% | 49 | 2.04% | 52 | 2% |
| Massary et al. (2019) | 78 | 0.71% | 78 | 2.58% | 78 | 3.25% | 45 | 1.73% |
| Etcheberry & Abraham (2009) | 77 | 0.7% | 71 | 2.35% | 71 | 2.96% | 53 | 2.04% |
| Dewynter & Claessens (2020) | 73 | 0.66% | 71 | 2.35% | 69 | 2.88% | 55 | 2.12% |
| Fraga & Carvalho (2021) | 73 | 0.66% | 70 | 2.31% | 70 | 2.92% | 57 | 2.19% |
| Bour et al. (2008) | 72 | 0.65% | 64 | 2.11% | 64 | 2.67% | 36 | 1.39% |
| Dickinson & Remsen (2013) | 72 | 0.65% | 60 | 1.98% | 47 | 1.96% | 54 | 2.08% |
| Dewynter (2018) | 70 | 0.63% | 66 | 2.18% | 66 | 2.75% | 66 | 2.54% |
| Charrassin (2016) | 69 | 0.62% | 65 | 2.15% | 65 | 2.71% | 48 | 1.85% |
| Charrassin (2016) | 69 | 0.62% | 65 | 2.15% | 65 | 2.71% | 48 | 1.85% |
| Moutou (2016) | 69 | 0.62% | 65 | 2.15% | 65 | 2.71% | 48 | 1.85% |
| Thoisy & Bordin (2016) | 69 | 0.62% | 65 | 2.15% | 65 | 2.71% | 48 | 1.85% |
| Urtizberea (2016) | 69 | 0.62% | 65 | 2.15% | 65 | 2.71% | 48 | 1.85% |
| Jarrett & Shirihai (2014) | 68 | 0.62% | 62 | 2.05% | 62 | 2.59% | 45 | 1.73% |
| Spitz et al. (2016) | 68 | 0.62% | 64 | 2.11% | 64 | 2.67% | 47 | 1.81% |
| Belfan & Conde (2016) | 62 | 0.56% | 58 | 1.92% | 55 | 2.29% | 46 | 1.77% |
| Aulagnier et al. (2017) | 61 | 0.55% | 55 | 1.82% | 55 | 2.29% | 40 | 1.54% |
| Faille et al. (2023) | 58 | 0.52% | 58 | 1.92% | 58 | 2.42% | 42 | 1.62% |
| Muratet (2015) | 53 | 0.48% | 47 | 1.55% | 27 | 1.13% | 36 | 1.39% |
| Massary et al. (2021) | 50 | 0.45% | 50 | 1.65% | 25 | 1.04% | 43 | 1.65% |
| Van Dijk et al. (2012) | 50 | 0.45% | 32 | 1.06% | 28 | 1.17% | 28 | 1.08% |
| Fouquet et al. (2019) | 48 | 0.43% | 47 | 1.55% | 47 | 1.96% | 47 | 1.81% |
| Santamaria & Faille (2007) | 48 | 0.43% | 20 | 0.66% | 14 | 0.58% | 16 | 0.62% |
| CHN (2017) | 47 | 0.43% | 47 | 1.55% | 47 | 1.96% | 47 | 1.81% |
| Breuil (2002) | 46 | 0.42% | 25 | 0.83% | 15 | 0.63% | 19 | 0.73% |
| Gmelin (1788) | 46 | 0.42% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Linnaeus (1766) | 45 | 0.41% | 10 | 0.33% | 9 | 0.38% | 9 | 0.35% |
| Hedges & Conn (2012) | 42 | 0.38% | 23 | 0.76% | 23 | 0.96% | 19 | 0.73% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 42 | 0.38% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Derrick et al. (1987) | 41 | 0.37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter (2021) | 39 | 0.35% | 37 | 1.22% | 37 | 1.54% | 37 | 1.42% |
| Uicn et al. (2012) | 39 | 0.35% | 29 | 0.96% | 27 | 1.13% | 28 | 1.08% |
| Nicholson et al. (2012) | 38 | 0.34% | 26 | 0.86% | 11 | 0.46% | 23 | 0.88% |
| Uicn et al. (2020) | 36 | 0.33% | 36 | 1.19% | 36 | 1.5% | 28 | 1.08% |
| de Massary et al. (2015) | 35 | 0.32% | 33 | 1.09% | 33 | 1.38% | 14 | 0.54% |
| Linnaeus (1753) | 35 | 0.32% | 13 | 0.43% | 13 | 0.54% | 12 | 0.46% |
| Arthur & Lemaire (2015) | 34 | 0.31% | 34 | 1.12% | 34 | 1.42% | 29 | 1.12% |
| Dietz & Kiefer (2015) | 34 | 0.31% | 34 | 1.12% | 34 | 1.42% | 29 | 1.12% |
| Godineau & Pain (2007) | 33 | 0.3% | 33 | 1.09% | 33 | 1.38% | 28 | 1.08% |
| Miaud & Muratet (2018) | 33 | 0.3% | 30 | 0.99% | 30 | 1.25% | 19 | 0.73% |
| Duguet & Melki (2003) | 32 | 0.29% | 21 | 0.69% | 21 | 0.88% | 15 | 0.58% |
| Kwet (2009) | 32 | 0.29% | 26 | 0.86% | 26 | 1.08% | 19 | 0.73% |
| Lafranchis (2014) | 32 | 0.29% | 21 | 0.69% | 21 | 0.88% | 15 | 0.58% |
| Lafranchis (2016) | 32 | 0.29% | 21 | 0.69% | 21 | 0.88% | 15 | 0.58% |
| Serre-collet (2013) | 32 | 0.29% | 30 | 0.99% | 30 | 1.25% | 20 | 0.77% |
| Bordin et al. (2021) | 31 | 0.28% | 31 | 1.02% | 31 | 1.29% | 21 | 0.81% |
| Garrigue (2007) | 31 | 0.28% | 31 | 1.02% | 30 | 1.25% | 23 | 0.88% |
| Thirion & Evrard (2012) | 31 | 0.28% | 25 | 0.83% | 25 | 1.04% | 18 | 0.69% |
| Glöer (2022) | 29 | 0.26% | 24 | 0.79% | 14 | 0.58% | 24 | 0.92% |
| Linnaeus (1753) | 29 | 0.26% | 20 | 0.66% | 18 | 0.75% | 15 | 0.58% |
| Laurenti (1768) | 28 | 0.25% | 5 | 0.17% | 3 | 0.13% | 3 | 0.12% |
| Uicn et al. (2015) | 28 | 0.25% | 25 | 0.83% | 25 | 1.04% | 22 | 0.85% |
| Catzeflis (2012) | 27 | 0.24% | 26 | 0.86% | 26 | 1.08% | 14 | 0.54% |
| Dewynter (2021) | 27 | 0.24% | 27 | 0.89% | 26 | 1.08% | 22 | 0.85% |
| Gargominy (2011-2023) | 27 | 0.24% | 27 | 0.89% | 19 | 0.79% | 27 | 1.04% |
| Welter-schultes (2012) | 27 | 0.24% | 23 | 0.76% | 23 | 0.96% | 18 | 0.69% |
| Dewynter et al. (2019) | 26 | 0.24% | 26 | 0.86% | 22 | 0.92% | 23 | 0.88% |
| Houard & Jaulin (2018) | 26 | 0.24% | 25 | 0.83% | 25 | 1.04% | 17 | 0.65% |
| Rocamora (2004) | 26 | 0.24% | 23 | 0.76% | 22 | 0.92% | 21 | 0.81% |
| Barau et al. (2005) | 25 | 0.23% | 20 | 0.66% | 20 | 0.83% | 16 | 0.62% |
| G.E.M.M. (2012) | 25 | 0.23% | 25 | 0.83% | 25 | 1.04% | 17 | 0.65% |
| Tronquet (2014) | 25 | 0.23% | 19 | 0.63% | 8 | 0.33% | 18 | 0.69% |
| Linné (1766) | 24 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tricart & Foubert (2000) | 24 | 0.22% | 22 | 0.73% | 22 | 0.92% | 22 | 0.85% |
| Dewynter et al. (2021) | 23 | 0.21% | 23 | 0.76% | 23 | 0.96% | 18 | 0.69% |
| Gannier (2001) | 23 | 0.21% | 23 | 0.76% | 23 | 0.96% | 15 | 0.58% |
| Weimerskirch et al. (2009) | 23 | 0.21% | 18 | 0.59% | 18 | 0.75% | 10 | 0.38% |
| Dewynter et al. (2023) | 22 | 0.2% | 22 | 0.73% | 22 | 0.92% | 19 | 0.73% |
| Fournier (1934-1940) | 22 | 0.2% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Clements et al. (2015) | 21 | 0.19% | 21 | 0.69% | 13 | 0.54% | 15 | 0.58% |
| Del Hoyo & Collar (2014) | 21 | 0.19% | 14 | 0.46% | 10 | 0.42% | 14 | 0.54% |
| Kerney & Cameron (1999) | 21 | 0.19% | 20 | 0.66% | 19 | 0.79% | 17 | 0.65% |
| Perrin et al. (2002) | 21 | 0.19% | 18 | 0.59% | 16 | 0.67% | 13 | 0.5% |
| Faivovich et al. (2005) | 20 | 0.18% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Fournet (2002) | 20 | 0.18% | 20 | 0.66% | 20 | 0.83% | 8 | 0.31% |
| Ingels et al. (2003) | 20 | 0.18% | 18 | 0.59% | 18 | 0.75% | 15 | 0.58% |
| Massary et al. (2017) | 20 | 0.18% | 17 | 0.56% | 16 | 0.67% | 15 | 0.58% |
| Shirihai (2003) | 20 | 0.18% | 16 | 0.53% | 15 | 0.63% | 11 | 0.42% |
| Commission de l’Avifaune Française (2016) | 19 | 0.17% | 18 | 0.59% | 18 | 0.75% | 16 | 0.62% |
| Dentant et al. (2018) | 19 | 0.17% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Dewynter et al. (2022) | 19 | 0.17% | 19 | 0.63% | 19 | 0.79% | 17 | 0.65% |
| Tapiero et al. (2017) | 19 | 0.17% | 19 | 0.63% | 19 | 0.79% | 15 | 0.58% |
| Dewynter et al. (2023) | 18 | 0.16% | 18 | 0.59% | 18 | 0.75% | 16 | 0.62% |
| Gannier (2002) | 18 | 0.16% | 18 | 0.59% | 18 | 0.75% | 14 | 0.54% |
| Gannier (2009) | 18 | 0.16% | 18 | 0.59% | 18 | 0.75% | 13 | 0.5% |
| Karadjian et al. (2022) | 18 | 0.16% | 18 | 0.59% | 18 | 0.75% | 13 | 0.5% |
| Kiszka et al.(2007) | 18 | 0.16% | 16 | 0.53% | 16 | 0.67% | 12 | 0.46% |
| Massary et al. (2018) | 18 | 0.16% | 17 | 0.56% | 16 | 0.67% | 15 | 0.58% |
| Boeters et al. (1989) | 17 | 0.15% | 11 | 0.36% | 11 | 0.46% | 8 | 0.31% |
| Euro+Med (2006) | 17 | 0.15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel et al. (2023) | 17 | 0.15% | 17 | 0.56% | 17 | 0.71% | 15 | 0.58% |
| Questel et al. (2023) | 17 | 0.15% | 17 | 0.56% | 17 | 0.71% | 15 | 0.58% |
| Salisbury (1796) | 17 | 0.15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breuil (2009) | 16 | 0.14% | 11 | 0.36% | 11 | 0.46% | 8 | 0.31% |
| Deblock et al. (1960) | 16 | 0.14% | 8 | 0.26% | 8 | 0.33% | 7 | 0.27% |
| Dewynter et al. (2019) | 16 | 0.14% | 15 | 0.5% | 15 | 0.63% | 13 | 0.5% |
| Gannier (2000) | 16 | 0.14% | 16 | 0.53% | 16 | 0.67% | 11 | 0.42% |
| Kiszka et al. (2010) | 16 | 0.14% | 15 | 0.5% | 15 | 0.63% | 12 | 0.46% |
| Kuntze (1891) | 16 | 0.14% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Mertens (1957) | 16 | 0.14% | 5 | 0.17% | 3 | 0.13% | 4 | 0.15% |
| Samaran & Guinet (2009) | 16 | 0.14% | 14 | 0.46% | 12 | 0.5% | 10 | 0.38% |
| Caziot (1903) | 15 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colin (1994) | 15 | 0.14% | 10 | 0.33% | 10 | 0.42% | 5 | 0.19% |
| Furminieux (2019) | 15 | 0.14% | 15 | 0.5% | 15 | 0.63% | 13 | 0.5% |
| Gouillard (1973) | 15 | 0.14% | 6 | 0.2% | 6 | 0.25% | 4 | 0.15% |
| Pallas (1776) | 15 | 0.14% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Szpigel (2024) | 15 | 0.14% | 13 | 0.43% | 13 | 0.54% | 11 | 0.42% |
| Ausilio & Zotier (1989) | 14 | 0.13% | 13 | 0.43% | 13 | 0.54% | 11 | 0.42% |
| Bonnier & Layens (1894) | 14 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desbrosses & Etcheberry (1987) | 14 | 0.13% | 11 | 0.36% | 11 | 0.46% | 4 | 0.15% |
| Dubois et al. (2008) | 14 | 0.13% | 13 | 0.43% | 13 | 0.54% | 12 | 0.46% |
| Dulau-Drouot et al. (2008) | 14 | 0.13% | 14 | 0.46% | 14 | 0.58% | 10 | 0.38% |
| Genoways et al. (2007) | 14 | 0.13% | 14 | 0.46% | 6 | 0.25% | 8 | 0.31% |
| Tarrier (2021) | 14 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Dijk et al. (2014) | 14 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boddaert & Daubenton (1783) | 13 | 0.12% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Breuil (1982) | 13 | 0.12% | 8 | 0.26% | 8 | 0.33% | 5 | 0.19% |
| [Denis & Schiffermüller] (1775) | 13 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faille et al. (2010) | 13 | 0.12% | 11 | 0.36% | 11 | 0.46% | 7 | 0.27% |
| Korb (2013) | 13 | 0.12% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Laran et al. (2011) | 13 | 0.12% | 13 | 0.43% | 13 | 0.54% | 10 | 0.38% |
| Wiersema et al. (2018) | 13 | 0.12% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Curado et al. (2011) | 12 | 0.11% | 11 | 0.36% | 11 | 0.46% | 4 | 0.15% |
| Dewynter et al. (2017) | 12 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Genest (1983) | 12 | 0.11% | 6 | 0.2% | 6 | 0.25% | 6 | 0.23% |
| Grazziotin et al. (2012) | 12 | 0.11% | 10 | 0.33% | 10 | 0.42% | 7 | 0.27% |
| Hodgetts & Lockhart (2020) | 12 | 0.11% | 12 | 0.4% | 12 | 0.5% | 12 | 0.46% |
| Korb et al. (2016) | 12 | 0.11% | 8 | 0.26% | 2 | 0.08% | 8 | 0.31% |
| Tostain (1980) | 12 | 0.11% | 8 | 0.26% | 8 | 0.33% | 6 | 0.23% |
| Ulloa et al. (2019) | 12 | 0.11% | 11 | 0.36% | 11 | 0.46% | 11 | 0.42% |
| Boer et al. (1999) | 11 | 0.1% | 10 | 0.33% | 9 | 0.38% | 8 | 0.31% |
| Brehm (1831) | 11 | 0.1% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Dubois (2017) | 11 | 0.1% | 11 | 0.36% | 11 | 0.46% | 11 | 0.42% |
| Girard (2007) | 11 | 0.1% | 7 | 0.23% | 7 | 0.29% | 6 | 0.23% |
| Hill et al. (2006) | 11 | 0.1% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Hugonnot et al. (2017) | 11 | 0.1% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Joyeux & Baer (1955) | 11 | 0.1% | 5 | 0.17% | 5 | 0.21% | 4 | 0.15% |
| Prévost & Mougin (1970) | 11 | 0.1% | 9 | 0.3% | 8 | 0.33% | 7 | 0.27% |
| Robineau & Duhamel (2006) | 11 | 0.1% | 9 | 0.3% | 8 | 0.33% | 5 | 0.19% |
| Rouy (1913) | 11 | 0.1% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Safford & Hawkins (2013) | 11 | 0.1% | 11 | 0.36% | 10 | 0.42% | 10 | 0.38% |
| Sennikov & Kurtto (2017) | 11 | 0.1% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Todd (1920) | 11 | 0.1% | 6 | 0.2% | 2 | 0.08% | 6 | 0.23% |
| Adalsteinsson et al. (2009) | 10 | 0.09% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Boer (2000) | 10 | 0.09% | 8 | 0.26% | 7 | 0.29% | 4 | 0.15% |
| Boissinot (2009) | 10 | 0.09% | 8 | 0.26% | 6 | 0.25% | 7 | 0.27% |
| Burneleau (1983) | 10 | 0.09% | 5 | 0.17% | 5 | 0.21% | 4 | 0.15% |
| Cambecèdes et al. (2012) | 10 | 0.09% | 8 | 0.26% | 7 | 0.29% | 8 | 0.31% |
| Cuvier & Valenciennes (1848) | 10 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Del Hoyo & Collar (2016) | 10 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril (1870) | 10 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupont (2010) | 10 | 0.09% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Escoriza et al. (2023) | 10 | 0.09% | 9 | 0.3% | 9 | 0.38% | 5 | 0.19% |
| Gill (1995) | 10 | 0.09% | 10 | 0.33% | 10 | 0.42% | 7 | 0.27% |
| Grand & Boudot (2007) | 10 | 0.09% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Grand et al. (2014) | 10 | 0.09% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Houard (2020) | 10 | 0.09% | 10 | 0.33% | 10 | 0.42% | 10 | 0.38% |
| Lichtenstein (1823) | 10 | 0.09% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Miller (1768) | 10 | 0.09% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Pedersen et al. (2013) | 10 | 0.09% | 9 | 0.3% | 9 | 0.38% | 2 | 0.08% |
| Prié (2017) | 10 | 0.09% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Ros et al. (2013) | 10 | 0.09% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Temminck et al. (1820-1840) | 10 | 0.09% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Trochet et al. (2024) | 10 | 0.09% | 10 | 0.33% | 6 | 0.25% | 7 | 0.27% |
| Vilette & Aucourd (2024) | 10 | 0.09% | 10 | 0.33% | 10 | 0.42% | 10 | 0.38% |
| Castroviejo-Fisher et al. (2011) | 9 | 0.08% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Chalumeau & Reid (2002) | 9 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2016) | 9 | 0.08% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Diaz & Cuzange (2009) | 9 | 0.08% | 7 | 0.23% | 7 | 0.29% | 5 | 0.19% |
| Dijkstra et al. (2015) | 9 | 0.08% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Dubois & Ohler (1994) | 9 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fouquet et al. (2021) | 9 | 0.08% | 9 | 0.3% | 9 | 0.38% | 9 | 0.35% |
| Greuter & Troia (2015) | 9 | 0.08% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Heidemann & Seidenbusch (2002) | 9 | 0.08% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Lacepède (1803) | 9 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moraes-da-silva et al. (2021) | 9 | 0.08% | 9 | 0.3% | 9 | 0.38% | 5 | 0.19% |
| Nicolas (1891) | 9 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nyman (1882) | 9 | 0.08% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Robineau (1989) | 9 | 0.08% | 5 | 0.17% | 4 | 0.17% | 3 | 0.12% |
| Scopoli (1769) | 9 | 0.08% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Spix (1825) | 9 | 0.08% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Thibault et al. (2014) | 9 | 0.08% | 9 | 0.3% | 9 | 0.38% | 8 | 0.31% |
| Wahlsteen & Tyler (2019) | 9 | 0.08% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Albouy & Richard (2017) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 3 | 0.12% |
| Blanc (1909) | 8 | 0.07% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Dewynter et al. (2016) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Doucet (2016) | 8 | 0.07% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Duguet (2022) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 7 | 0.27% |
| Dujardin (1956) | 8 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guth (1971) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 5 | 0.19% |
| Leraut (2012) | 8 | 0.07% | 7 | 0.23% | 7 | 0.29% | 0 | 0% |
| Orrico et al. (2017) | 8 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
| pallas (1764) | 8 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philcox (1965) | 8 | 0.07% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Pontoppidan (1763) | 8 | 0.07% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Powell & Henderson (2023) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 7 | 0.27% |
| Probst (1997) | 8 | 0.07% | 7 | 0.23% | 7 | 0.29% | 5 | 0.19% |
| Reynolds & Henderson (2018) | 8 | 0.07% | 6 | 0.2% | 5 | 0.21% | 4 | 0.15% |
| Rouy (1908) | 8 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santos et al. (2023) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Sturaro et al. (2020) | 8 | 0.07% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Temminck et al. (1838) | 8 | 0.07% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Thumsová et al. (2022) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 5 | 0.19% |
| Troia & Rouhan (2018) | 8 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2011) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 8 | 0.31% |
| Vieira (2022) | 8 | 0.07% | 8 | 0.26% | 8 | 0.33% | 5 | 0.19% |
| Béarez et al. (2017) | 7 | 0.06% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Bernal & Dubois (2023) | 7 | 0.06% | 6 | 0.2% | 6 | 0.25% | 4 | 0.15% |
| Bochaton et al. (2021) | 7 | 0.06% | 7 | 0.23% | 7 | 0.29% | 4 | 0.15% |
| Cabidoche (1968) | 7 | 0.06% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Camiñas et al. (2021) | 7 | 0.06% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Dewynter et al. (2017) | 7 | 0.06% | 7 | 0.23% | 7 | 0.29% | 7 | 0.27% |
| Duméril & Bribron (1841) | 7 | 0.06% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Esper & Charpentier (1789-[1804]) | 7 | 0.06% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Esper (1780-1786) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geniez & Cheylan (2012) | 7 | 0.06% | 3 | 0.1% | 0 | 0% | 3 | 0.12% |
| Lazell (1964) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muñoz et al. (2013) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortiz et al. (2022) | 7 | 0.06% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Pinto-coelho et al. (2021) | 7 | 0.06% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Rossi-santos et al. (2007) | 7 | 0.06% | 5 | 0.17% | 5 | 0.21% | 3 | 0.12% |
| Rouy & Foucaud (1893) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schweigger (1812) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souza-oliveira et al. (2024) | 7 | 0.06% | 6 | 0.2% | 6 | 0.25% | 4 | 0.15% |
| Spix (1824) | 7 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spix (1824) | 7 | 0.06% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Aubouin et al. (2016) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 3 | 0.12% |
| Bernasconi (1989) | 6 | 0.05% | 4 | 0.13% | 2 | 0.08% | 4 | 0.15% |
| Bichain et al. (2007) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonaparte (1832-1841) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Bonnet et al. (1999) | 6 | 0.05% | 3 | 0.1% | 3 | 0.13% | 1 | 0.04% |
| Cariot & Saint-lager (1889) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Casale et al. (2021) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 6 | 0.23% |
| Claessens et al. (2014) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 5 | 0.19% |
| Coiffait (1969) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier (1829) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1802) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Dewynter et al. (2020) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 6 | 0.23% |
| Dillenberger & Kadereit (2014) | 6 | 0.05% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dória et al. (2015) | 6 | 0.05% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Dulac (1867) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fretey & Triplet (2022) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 6 | 0.23% |
| Frost et al. (2006) | 6 | 0.05% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Funk et al. (2007) | 6 | 0.05% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Girardi (2009) | 6 | 0.05% | 6 | 0.2% | 0 | 0% | 6 | 0.23% |
| Godet et al. (2021) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 2 | 0.08% |
| Goicoechea et al. (2016) | 6 | 0.05% | 4 | 0.13% | 4 | 0.17% | 2 | 0.08% |
| Graitson et al. (2012) | 6 | 0.05% | 4 | 0.13% | 4 | 0.17% | 2 | 0.08% |
| Gray (1821) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1866) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heppner (1981) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Holenweg Peter (2001) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jeannel (1938) | 6 | 0.05% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Lamarck (1779) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1787) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lazell (1972) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindner (1859) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Mériguet & Zagatti (2016) | 6 | 0.05% | 6 | 0.2% | 6 | 0.25% | 1 | 0.04% |
| Pallas (1773) | 6 | 0.05% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Schneider (1799) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thomas (1964) | 6 | 0.05% | 5 | 0.17% | 0 | 0% | 5 | 0.19% |
| Ugelvig et al. (2011) | 6 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli (2021) | 6 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Almeida et al. (2024) | 5 | 0.05% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Arcangeli (1882) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbrour (1915) | 5 | 0.05% | 3 | 0.1% | 2 | 0.08% | 2 | 0.08% |
| Barre et al. (2009) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 4 | 0.15% |
| Barrioz & Morinière (2007) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Bedriaga (1883) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Billi et al. (2011) | 5 | 0.05% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Bioinsight/diren & Guyane (2006) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Boer & Simmonds (2000) | 5 | 0.05% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Borsa (1997) | 5 | 0.05% | 4 | 0.13% | 3 | 0.13% | 2 | 0.08% |
| Breuil et al. (2010) | 5 | 0.05% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Brunes et al. (2021) | 5 | 0.05% | 4 | 0.13% | 4 | 0.17% | 1 | 0.04% |
| Chevalier (2006) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Ciccione et al. (2011) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Cope (1868) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crillon & Cuzange (2020) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Danihelka et al. (2010) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Danihelka et al. (2010) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Descimon et al. (2001) | 5 | 0.05% | 5 | 0.17% | 1 | 0.04% | 4 | 0.15% |
| Díaz et al. (1996) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Duffaut et al. (2011) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Dufresnes et al. (2024) | 5 | 0.05% | 5 | 0.17% | 3 | 0.13% | 4 | 0.15% |
| Dupont (2010) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Entraygues (2014) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Étaix-bonnin et al. (2011) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Etheridge (2010) | 5 | 0.05% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Fischer et al. (2013) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Fouquet et al. (2015) | 5 | 0.05% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fourès (1954) | 5 | 0.05% | 5 | 0.17% | 4 | 0.17% | 4 | 0.15% |
| Fritz (1995) | 5 | 0.05% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Fruhstorfer (1921) | 5 | 0.05% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Gory (1995) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Guermeur (1987) | 5 | 0.05% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Guiller & Vacher (2022) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Hamdan et al. (2023) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Heimer & Frajman (2023) | 5 | 0.05% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Hequet & Le Corre (2010) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Hequet et al. (2009) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Holsbeek et al. (2008) | 5 | 0.05% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Isler et al. (2013) | 5 | 0.05% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| IUCN (2012) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 3 | 0.12% |
| Kasamatsu & Joyce (1995) | 5 | 0.05% | 4 | 0.13% | 3 | 0.13% | 4 | 0.15% |
| Larsen et al. (2006) | 5 | 0.05% | 5 | 0.17% | 0 | 0% | 5 | 0.19% |
| Le Scao et al. (2011) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Locard (1893) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopes-Lima et al. (2016) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacKee (1994) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 2 | 0.08% |
| Massary et al. (2020) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Nussbaum & Hoogmoed (1979) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Ochs (1938) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Pallas (1769) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas [1814] | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1831) | 5 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelzeln (1868) | 5 | 0.05% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Potin (2013) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Préau et al. (2017) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 3 | 0.12% |
| Probst et al. (2022) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Read & Farman (2018) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Read et al. (2023) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Rhodin et al. (2017) | 5 | 0.05% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Riccialdelli et al. (2010) | 5 | 0.05% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Rico et al. (2006) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Robineau (2005) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 1 | 0.04% |
| Routtier et al. (2023) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 1 | 0.04% |
| Sauvignet et al. (2000) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Schlegel (1837) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Schwartz (1964) | 5 | 0.05% | 3 | 0.1% | 0 | 0% | 3 | 0.12% |
| Stewart (2014) | 5 | 0.05% | 5 | 0.17% | 0 | 0% | 5 | 0.19% |
| Thiollay (2007) | 5 | 0.05% | 5 | 0.17% | 5 | 0.21% | 5 | 0.19% |
| Vieillot (1819) | 5 | 0.05% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Zelhuber (2009) | 5 | 0.05% | 5 | 0.17% | 4 | 0.17% | 4 | 0.15% |
| Albuquerque et al. (2022) | 4 | 0.04% | 4 | 0.13% | 2 | 0.08% | 2 | 0.08% |
| Alvarez-berríos et al. (2016) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Arredondo et al. (2020) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Arribas (1999) | 4 | 0.04% | 4 | 0.13% | 2 | 0.08% | 2 | 0.08% |
| Baker et al. (1978) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Bangs & Penard (1921) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Banks et al. (2006) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Barbraud et al. (2009) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Berta & Churchill (2012) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boie (1827) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boistel et al. (2006) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Booister (2009) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borczyk et al. (2022) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 1 | 0.04% |
| Bost et al. (2022) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 2 | 0.08% |
| Bravo et al. (2012) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Breuil & Ibéné (2008) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Brown et al. (2011) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brünnich (1764) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Callot-Girardi (2015) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carrasco et al. (2012) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Carrillo (2023) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Carvalho et al. (2023) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Castro et al. (2018) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Cecchi et al. (2014) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Cole & Dessauer (1993) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Daudin (1800) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1803) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delord et al. (2005) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Delord et al. (2008) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Deméré (2014) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Denis (2011) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Denys et al. (2014) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Dewynter et al. (2016) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Dewynter (2016) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Dewynter (2020) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 1 | 0.04% |
| Dickinson & Christidis (2014) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Draparnaud (1805) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duellman et al. (2016) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dufresnes et al. (2024) | 4 | 0.04% | 4 | 0.13% | 2 | 0.08% | 4 | 0.15% |
| Duguy (1988) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Duguy (1994) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Duguy (1997) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Duméril & Bibron (1837) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril et al. (1854) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1849) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ehrhardt (1971) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Eisner (1957) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Erard et al. (1991) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Esper & Charpentier (1789-[1804]) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faille & Bourdeau (2022) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Folin & Bérillon (1877) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Forster (1781) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fouquet et al. (2019) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fourt et al. (2017) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Fretey & Lescure (1999) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Fritz & Schmidtler (2020) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Gargominy & Ripken (2006) | 4 | 0.04% | 3 | 0.1% | 1 | 0.04% | 3 | 0.12% |
| Gazoni et al. (2021) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Girardi (2009) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Gmelin (1789) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Göktürk & Sümbül (2014) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Grant et al. (2006) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Grenier & Godron (1850) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heinicke et al. (2007) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Heyer & de Sá (2011) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Hodges et al. (2024) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 1 | 0.04% |
| Iglesias-carrasco et al. (2017) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 2 | 0.08% |
| Isenmann et al. (1971) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| IUCN (2013) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Jeannel (1913) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Jeannel (1916) | 4 | 0.04% | 3 | 0.1% | 2 | 0.08% | 2 | 0.08% |
| Jeannel (1919) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Fourreau (1869-1903) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kallel et al. (2018) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Keith et al. (2011) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Kindler et al. (2017) | 4 | 0.04% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Kitchener et al. (2017) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Köhler & Vesely (2011) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Kok et al. (2006) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| La Cepède (1789) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck & Candolle (1805) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lamarck (1779) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latham (1790) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lefranc & Issa (2013) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 3 | 0.12% |
| Lepechin (1769) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linossier et al. (2017) | 4 | 0.04% | 4 | 0.13% | 0 | 0% | 4 | 0.15% |
| Loiseleur-deslongchamps (1807) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macleod et al. (2006) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Massary & Hoogmoed (2001) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Matsuoka et al. (2005) | 4 | 0.04% | 4 | 0.13% | 3 | 0.13% | 2 | 0.08% |
| Mazel (1982) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meek (2021) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 1 | 0.04% |
| Méheust et al. (2018) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Momont (1998) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Morel (1959) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Morinière & Dell'amico (2011) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Oberthür (1910) | 4 | 0.04% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Olson & Normand (2014) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Paladilhe (1869) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paradis et al. (2018) | 4 | 0.04% | 4 | 0.13% | 1 | 0.04% | 3 | 0.12% |
| Pellegrino et al. (2018) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Perreau & Queinnec (1987) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Plötner et al. (2012) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Probst (1997) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Probst (2001) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Rivas et al. (2024) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Rojas-runjaic et al. (2021) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Rottemburg (1775) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1895) | 4 | 0.04% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Saint & Girons (1976) | 4 | 0.04% | 3 | 0.1% | 0 | 0% | 3 | 0.12% |
| Sayah et al. (2023) | 4 | 0.04% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Schiebel (1910) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schneider (1801) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Serrano et al. (2016) | 4 | 0.04% | 3 | 0.1% | 2 | 0.08% | 1 | 0.04% |
| Souza (2020) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Starace (2013) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Swanepoel & Genoways (1983) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 0 | 0% |
| Temminck et al. (1838) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Temminck et al. (1838) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 4 | 0.15% |
| Testout (1943) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiébaut & Tison (2016) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele et al. (1999) | 4 | 0.04% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Tostain & Dujardin (1988) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Tostain (1986) | 4 | 0.04% | 4 | 0.13% | 4 | 0.17% | 2 | 0.08% |
| Une et al. (1817) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ursenbacher et al. (2006) | 4 | 0.04% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Verity (1920) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verity (1928) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagler (1830) | 4 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Walbaum (1792) | 4 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wilson (2016) | 4 | 0.04% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| AAMP (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Ainley et al. (2007) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Almeida et al. (2022) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Andres et al. (2014) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Anonyme (2014) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Argod-vallon (1913) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arntzen et al. (2016) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Arribas (2009) | 3 | 0.03% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Arribas (2019) | 3 | 0.03% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Aulagnier (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Bailon et al. (2015) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Barbraud et al. (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bauer & Sadlier (2000) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bechstein (1803) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Belcik et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bernasconi (1985) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Berv & Prum (2014) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Bischoff (2020) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Blat (2013) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bochaton & Hanot (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Boeters (1981) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Boettger (1949) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonacci et al. (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bonaccorso et al. (2011) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Bonnaterre (1789) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boucher et al. (2021) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Boulenger (1882) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Proceedings of the Zoological Society of London, 1883: 635-638.">Boulenger (1884) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Bour et al. (2017) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (2006) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1868) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broyer (2009) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Brustel & Gouix (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Bubani & Penzig (1897) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Busala et al. (2024) | 3 | 0.03% | 2 | 0.07% | 1 | 0.04% | 2 | 0.08% |
| Bussiere & Labrousse (2015) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Cadiou et al. (2010) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Capurucho et al. (2013) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Carravieri et al. (2016) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Carrillo et al. (2023) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Carstens et al. (2004) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Carvalho et al. (2015) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Carvalho et al. (2016) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Carvalho et al. (2022) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Catzeflis (2019) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Chabaud et al. (2022) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 3 | 0.12% |
| Cisneros-Heredia (2013) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Coiffait (1976) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collier et al. (2002) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 2 | 0.08% |
| Cottarel et al. (2013) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Coulon et al. (2011) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Csutoros (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Daudin (1803) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1803) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delaugerre & Guyot (1995) | 3 | 0.03% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Delcroix et al. (2011) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Della et al. (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Demay et al. (2023) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Deslandes (1930) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deso et al. (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 1 | 0.04% |
| Dieck (1869) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Don (1838) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Drillon et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Dubief & Gallais (2011) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (1998) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (1999) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (2000) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (2002) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (2006) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy et al. (2007) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy (1967) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Duguy (1990) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Duguy (1996) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Dumortier (1827) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupre (1991) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupuy (1847-1852) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Durant et al. (2013) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Easteal (1981) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Escoriza (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 1 | 0.04% |
| Euzet & Jourdane (1968) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Faggio et al. (2022) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Faille et al. (2010) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fouquet et al. (2007) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fouquet et al. (2018) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fouquet et al. (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fouquet et al. (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fourès (1961) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourreau (1868) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2005) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Fric et al. (2007) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fruhstorfer (1909) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fuchs et al. (2014) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Fukushima & Bertani (2017) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gamble et al. (2011) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Garrigues et al. (2020) | 3 | 0.03% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Gaudin (1938) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Gaudin (1947) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gayet et al. (2010) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Gebhardt‐Henrich et al. (1998) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Genard & Lescourret (1987) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Genest (1977) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot (2011) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Gmelin (1770) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gonzalez et al. (2009) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| González-sánchez et al. (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 1 | 0.04% |
| Grolle & Long (2000) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Hagenmüller (1888) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Han et al. (2010) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Hass (1991) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Hedges et al. (2014) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Hermann (1804) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Humphries et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| ICZN (2017) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Igea et al. (2015) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Jacquet (2009) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Jadin et al. (2014) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jan (1863) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jaworski et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Jeannel (1916) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jeannel (1938) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Jefferson & Rosenbaum (2014) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jordan (1864) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Joubert & Margerit (1986) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Jouventin et al. (1989) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kawamura (1994) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Kayser et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Knoepffler (1967) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kock et al. (2006) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Kolenda et al. (2024) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Kottelat (1997) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuo et al. (2019) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lamarck (1778) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lanza (1972) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laran et al. (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Latham (1790) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Leaper et al. (2008) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Leraut (1997) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescroel et al. (2009) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Lescure et al. (2020) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 3 | 0.12% |
| Lesson (1831) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Lesueur (1818) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Léveillé (1917) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Delcroix (2016) | 3 | 0.03% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Lidth de Jeude (1904) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Linnaeus (1759) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1763) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Litvinchuk et al. (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Lötters et al. (2022) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Louette & Cousin (1999) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Macculloch et al. (2009) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Martins et al. (2019) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Massa et al. (2015) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Mazzei et al. (2018) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Meier et al. (2023) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Merrem (1820) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meurgey & Ramage (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Meurgey (2006) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Meurgey (2011) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Mezhzherin et al. (2024) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Michaels et al. (2023) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Mignet et al. (2020) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Miralles & Carranza (2010) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miralles et al. (2017) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Moneglia et al. (2009) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Naulleau (1983) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Nelson-Smith et al. (2014) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Nevill (1879) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oberthür (1909) | 3 | 0.03% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Oliveira et al. (2016) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 2 | 0.08% |
| Oswald et al. (2022) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Pallas (1771) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1831) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Pedroso-santos et al. (2024) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Peloso et al. (2014) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Penloup et al. (1997) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Perrin et al. (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Persat et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Piry et al. (2018) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Poisson (1999) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Pomar-gómez et al. (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Pons et al. (2005) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Pottier (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Prelli & Boudrie (2021) | 3 | 0.03% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Probst (1998) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Pteridophyte Phylogeny Group (2016) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Raffaëlli (2007) | 3 | 0.03% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Réjaud et al. (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Read & Jean (2021) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Recuero et al. (2014) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Regan (1916) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Renner (2002) | 3 | 0.03% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Richter (1890) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodríguez-rodríguez & Calderón-espinosa (2024) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rönkä et al. (2016) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ronot (2007) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Ros et al. (2007) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Roughgarden (1995) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1903) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Sagar (1991) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Samaran (2008) | 3 | 0.03% | 3 | 0.1% | 1 | 0.04% | 2 | 0.08% |
| Sardet et al. (2015) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Scopoli (1763) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Selvi et al. (2009) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Sharpe (1894) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Socolovschi et al. (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Steindachner (1870) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Surget-Groba & Thorpe (2013) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Temminck (1818-1838) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 0 | 0% |
| Tenore (1811-1815) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiebot et al. (2011) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Thiele et al. (2004) | 3 | 0.03% | 3 | 0.1% | 2 | 0.08% | 2 | 0.08% |
| Thomaes et al. (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Thorpe & Malhotra (2023) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Thorpe et al. (2008) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Tremblay & Cherel (2005) | 3 | 0.03% | 3 | 0.1% | 0 | 0% | 3 | 0.12% |
| Troia et al. (2014) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Troschel (1848) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Tunstall (1880) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| UICN (2009) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Une et al. (1816) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Veith (1996) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Velazco & Patterson (2013) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Verity (1947) | 3 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vidal et al. (1999) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Vidal et al. (2010) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Vieillot (1817) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Villars (1789) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Vollmer et al. (2019) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Vrezec et al. (2017) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 3 | 0.12% |
| Williams et al. (2020) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 1 | 0.04% |
| Witt & Ronkay (2011) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Yang et al. (2021) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Yokoyama (2012) | 3 | 0.03% | 3 | 0.1% | 3 | 0.13% | 2 | 0.08% |
| Zocca et al. (2024) | 3 | 0.03% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Zuffi (2002) | 3 | 0.03% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| (2023) | 3 | 0.03% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Acheray (1937) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adams (1989) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Albouy et al. (2017) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Allioni (1785) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Altamirano-Benavides & Woolrich-Piña (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Altamirano-benavides & Woolrich-piña (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Amanajás et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Ambu et al. (2024) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Anonyme [BUFO] (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Anonyme (2023) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arntzen & Wallis (1991) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Arntzen (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Arntzen (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Arribas (1993) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arribas (2000) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Arroyo et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Asztalos et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Bachelard & Fournier (2010) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Baldi et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Balle et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Ballouard et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bannwarth & Dewynter (2015) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Bargain & Henry (2000) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Barré et al. (2016) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Bassitta et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Bauer & Powell (2024) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baumel et al. (2009) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bavoux et al. (1993) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Beaubrun (2004) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Bechstein (1792) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benedetti et al. (2021) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Bénito-espinal (1990) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bergsträsser (1779) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernarde et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Bernasconi (2000) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berrebi et al. (2018) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Birdlife International (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bischoff (1988) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Blanchet et al. (1998) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Blumenbach (1810) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton et al. (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Boeters & Falkner (2003) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Boeters (1983) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Böining et al. (2024) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Boisduval (1828) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boistel & Massary (1999) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonacci et al. (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bonnefond et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bonnier (1912) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boreau (1857) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bortolato (1988) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosc (1792) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boubée (1836) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchet et al. (1997) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Boudarel & Scher (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bourgade (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Bourguignat (1862) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourguignat (1864) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Bouton (1986) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Brambilla et al. (2008) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Branch et al. (2007) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Brasileiro (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Breuil (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Breuil (2013) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brodier et al. (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Brooks (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Brugneaux & Pérès (2006) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1902) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burgeff (1914) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Burger et al. (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Butler (1868) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabanis (1847) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Cabanis (1875) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Cabidoche (1965) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Cadle (2009) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calviño et al. (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Campbell & Clarke (1998) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Camurugi et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Candolle (1815) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1824) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1828) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caparella & Lanyon (1985) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Capocaccia (1964) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caramaschi (2010) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Carneiro et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Castiglia et al. (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Cecchi et al. (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Censky & Paulson (1992) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chaix (1785) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Champagne et al. (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Chanselme (1997) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 2 | 0.08% |
| Chappuis et al. (1974) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Charissou (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Chartier et al. (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Chartier (1989) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Chavatte et al. (2019) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Cheke (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Cherel et al. (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Cherel et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Chevallier et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Chevallier et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| ">Claes (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Clarac et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Claramunt (2014) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Clarke & Lanza (1990) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Clement & Chapalain (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Cocteau (1835) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colas (1948) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Collin (1913) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1864) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1869) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Correa & Artigas (1978) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cosson et al. (1994) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Costa et al. (2022) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Costa-campos et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Couch (1877) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Courant & Meme-Lafond (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Crouzier (2017) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Cunha et al. (2015) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Cupedo (1996) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| 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) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| dal Molin (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dal Vechioet al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| D'Amico (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| D'angiolella et al. (2011) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daniel et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Daniel (1939) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1801) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Daudin (1802) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davant (1967) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Debout (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Delalande (1994) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Delaugerre et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Delnatte & Meyer (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Denis et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Denoël & Ficetola (2007) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Derryberry et al. (2010) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Descimon (1995) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Desfontaines (1787) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desfontaines (1798) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deso (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Dierks (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dohogne (2003) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Döll (1843) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donegan (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Donovan (1816) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dorleans (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Doucet (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dronneau & Wassmer (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dubois & Ohler (1994) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois et al. (2000) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Dubois et al. (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Dubois (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dufour (2001) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Dufresnes et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Dufva & Allander (1996) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy et al. (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy et al. (2003) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy et al. (2004) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy (1986) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy (1992) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy (1993) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duguy (1995) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duhaldeborde (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Duhamel et al. (2005) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Duméril & Bibron (1836) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Duquet (2012) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Durand (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Eberhard et al. (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Eisner (1956) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eisner (1957) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Erard & Sabatier (1988) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Escalona et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Esper (1776-1779) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius ([1777]) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faille & Bourdeau (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Faille et al. (2013) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fernandes et al. (2004) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferrante et al. (2017) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Ferrão et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Figueira et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Fiori (1925) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fitzinger (1826) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fleuriau & Bosc (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Flora of North America (1993-) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fontanilles et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Formon (1975) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Fouquet et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Fouquet et al. (2011) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Fouquet et al. (2016) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourcy & Robert (1987) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Fourreau (1869) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Freitas (1958) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frétey & Pottier (2022) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Freyer (1836-1839) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritz & Havaš (2007) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frolet (2003) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Frugone et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Fruhstorfer (1906) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Gallien (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Galloo & Lourdais (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Gannier & Petiau (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Garoche & Sohier (2000) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Garoche & Sohier (2002) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Garoche & Sohier (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Garoche & Sohier (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Garrigue & Poupon (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Garrigue et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gasc & Rodrigues (1979) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gasc & Rodrigues (1979) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gasper et al. (2016) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gaudin (1925) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Gaudin (1939) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gazzola et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Gené (1839) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Genero (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Genest & Juberthie (1983) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geniez & Crochet (2003) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry et al. (2004) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Geoffroy (1762) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Georgi (1775) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gergaud et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Germain (1931) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Ghidotti et al. (2018) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Gibson & Baker (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gill & Thiele (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Gill (1883) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard-claudon & Ribatto (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Girardi & Bertrand (2009) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Girardi (2002) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondo (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gittenberger (1973) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1774) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goczal & Rossa (2017) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Godart (1822-[1824]) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Golvan (1956) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gomés et al. (2018) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 2 | 0.08% |
| Gomez & Voisin (2002) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Goodall et al. (1997) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gould (1844) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gourreau et al. (1998) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Grange et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gray (1851) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Green (1996) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Groen (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Grosser et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Guayasamin et al. (2009) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Guérin-Méneville (1855) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guiguen et al. (1984) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Guiller et al. (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Guiller et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Guillon et al. (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Gunnerus (1767) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Gutowski et al. (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gvoždík et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Gvoždík et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Hall (1900) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Hamilton (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Hanus & Theye (2010) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Hanus & Theye (2011) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hauk et al. (2003) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Head et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Heckel & Kner (1858) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedges et al. (2016) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hemming (1932) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Herón-royer (1884) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herrera-alva et al. (2020) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Hervé & François (1995) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heyer (1994) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Heyer (1995) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Heym et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Higgins (1978) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hirschke (1904-1905) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holyoak & Holyoak (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Honey & Scoble (2001) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Horak & Chobot (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Horak & Chobot (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Horak et al. (2010) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Hoser (2023) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hosner (2005) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Huang (2017) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Hübner ([1799-1800]) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Illiger (1803) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Imfeld et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Impact-mer (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Ingels et al. (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| International Commission on Zoological Nomenclature (1992) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Isenmann et al. (2000) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jablonski et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jadin et al. (2020) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Jardine & Selby (1826-1835) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jeffrey (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Jiguet (2002) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Johnson et al. (1988) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Jolinon (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Jordan & Fourreau (1866) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouan (1863) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jouard (1929) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jouard (1929) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jowers et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jullien & Cariveau (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jungfer & Hödl (2002) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Jungfer & Schiesari (1995) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Jungfer et al. (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Jutzeler (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Kaczmarek et al. (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Kaiser & Altig (1994) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaiser et al. (1994) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kasamatsu et al. (2000) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Kemp (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Kerbiriou et al. (2004) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Kerbiriou et al. (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Kesenheimer (1920) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling & Blasius (1839) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klaczko et al. (2010) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Knoch (1781) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Knox et al. (2002) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Kok & Castroviejo-fisher (2008) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Kollarits et al. (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Krug et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Krystufek (2017) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Krystufek (2017) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Kuemmerle (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Kuhl (1820) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kupfer & Kneitz (2000) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| La Cepède (1788) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1800) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lack & Lack (1951) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Ladent et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Lajonquière (1965) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1789) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lambert (1988) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lang (2010) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Lanza & Brizzi (1974) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Lanza et al. (1984) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lanza et al. (1986) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lapeyrouse (1813) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapous (1988) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Latreille & Godart (1819-[1824]) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latreille (1800) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavauden (1929) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavilla et al. (2003) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lavilla et al. (2010) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Le Cerf (1913) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Charles (1933) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Leaper et al. (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Leboulenger (1989) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lee & Walsh-McGehee (2000) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Leisler (1812-1813) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesaffre (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lescroel et al. (2004) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lescure (1975) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Leskovar & Sinsch (2005) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1841) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letacq (1924) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levesque & Clergeau (2002) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Levesque & Delcroix (2013) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Link (1829) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1764) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1771) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopes & Gonzaga (2016) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lopes et al. (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Loret & Barrandon (1876) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec et al. (2004) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Lorvelec et al. (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Lorvelec et al. (2021) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lötters et al. (2002) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lötters et al. (2011) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lourdais et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Lovaty (2002) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Lustrat (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Lynch & Hoogmoed (1977) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maciel & Hoogmoed (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Maciel et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Malmgren (2002) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Mann et al. (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Manns & Anderberg (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Maran & Frétey (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Maréchal (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Marquant (1959) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martinet et al. (1765) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martinet et al. (1765) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martins et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Mathews (1912) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Mathews (1914) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Mays et al. (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Mazel (1979) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mckitrick (1985) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Mees (1987) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Melo-sampaio et al. (2019) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Meurgey & Picard (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Meurgey (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Meynard (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Meynier (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Miller (1908) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Millet (1828) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat & Veillon (1985) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Morat et al. (2012) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Moravec et al. (2018) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Müller (1774) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1776) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller 1924 | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Munzinger et al. (2016) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Murphy et al. (1978) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murphy et al. (2019) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Myers & Cadle (1994) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Naciri et al. (2017) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Naulleau & Bonnet (1995) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Naveira et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Nazari et al. (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Nipkow (1990) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Oberthür (1913) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oberthür (1922) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliver (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Oremus (2009) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 2 | 0.08% |
| Oulès (2019) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Pabijan et al. (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Pagenstecher (1909) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Pallas (1769) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parise et al. (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Parker (1940) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Pascal & Touroult (2015) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Pascal et al. (2006) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Paul & Lefranc (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Payraudeau (1826) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pedall et al. (2010) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Peron (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Persoon (1805) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1863) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1867) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pezy et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Pictet (1843) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierret (1838) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Pilorge & Xavier (1981) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinston & Craney (1991) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 2 | 0.08% |
| Pintér (1983) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Pokrant et al. (2016) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Pöschel et al. (2018) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Powell et al. (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Prampart (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Praviel (1936) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Prié & Cucherat (2021) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prieto et al. (2012) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst et al. (2000) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Probst et al. (2001) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Proćków & Drábková (2023) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Purenne (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Questel (2011) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raffaëlli (1983) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Raffaëlli (2020) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Rathgeber & Bayle (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Raust & Sanford (2007) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Raynaud (1959) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Reichenow (1904) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reilly et al. (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Remsen et al. (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Renaudier et al. (2010) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Renner (1997) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rheindt et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Ridoux (1989) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Riina et al. (2013) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Rinaldi et al. (2011) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Risso (1816) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau et al. (2007) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Robineau (2004) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Rochelet (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Rojas-morales et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Romanova et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Rossmässler & Kobelt (1906) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rossmässler (1854) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rougeot (1990) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roughgarden (1974) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux et al. (1983) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux (1913) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Rouy & Camus (1901) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1897) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1912) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rykena (1991) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Sabine (1819) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| SACC (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Saint et al. (1978) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Salvidio et al. (1997) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Salvin (1896) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Samaran & Guinet (2010) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Samaran et al. (2010) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Sangster et al. (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Santos et al. (2019) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Santos (2003) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Savi (1838) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidtler & Böhme (2011) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Schmitz et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Schneider (1783) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schreber (1774) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schultze et al. (2020) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Schwartz & Thomas (1975) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sclater (1866) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Scopoli (1786) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Searby & Jouventin (2005) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Seglie & Evangelista (2010) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sentzen (1796) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1802) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Sheldon et al. (2005) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Shuttleworth (1843) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Silva (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Silveira & Magnusson (1999) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Simmons (2005) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Slager & Klicka (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Sobral et al. (2019) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Socha & Ogielska (2010) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Soubeyran (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Spach (1838) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speare (1990) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speybroeck et al. (2010) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spitz et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Spix (1824) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stahl et al. (1985) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Starace (1995) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Staudinger & Wocke (1861) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1864) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart (2014) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Stichel (1908) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stynoski et al. (2015) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Swainson (1838) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Taberlet (1983) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Tatin et al. (2003) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Tello et al. (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Temminck et al. (1838) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Tennyson et al. (2022) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Thibault et al. (1987) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Thibault et al. (2023) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Thomas et al. (2021) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Thorpe et al. (2010) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thunberg (1787) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Timm & Genoways (2003) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Tirvengadum & Bour (1985) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Todd (1925) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Todd (1931) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Todd (1937) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Todisco et al. (2012) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Torres-ramírez et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Tostain (1987) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Tostain (1988) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Tremauville (1991) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Tremblay & Cherel (2003) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Tremblay et al. (2004) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tremetsberger et al. (2002) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Trotignon et al. (1994) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tutin et al. (1972) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tylkowski (2014) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Uicn et al. (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Uicn et al. (2017) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| UNEP-WCMC (2005) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Šunje et al. (2021) | 2 | 0.02% | 2 | 0.07% | 1 | 0.04% | 1 | 0.04% |
| Uvarov (1923) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vacher et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Vamberger et al. (2015) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Van Canneytet al. (2008) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| van den Burg et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Vanderwerf et al. (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Verbeek (1984) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Vieillot (1817) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Vieillot (1819) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Viette (1961) | 2 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Villanueva et al. (2021) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Villard et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Villars (1787) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Villers (1789) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villers (1789) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Visser et al. (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Voisin & Voisin (2001) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin & Voisin (2001) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Voisin (1971) | 2 | 0.02% | 2 | 0.07% | 0 | 0% | 2 | 0.08% |
| Wallach et al. (2014) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Wallis & Arntzen (1989) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Waugh & Weimerskirch (2003) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weimerskirch et al. (2009) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Weller (2000) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wells & Inskipp (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Wenner et al. (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Westcott & Smith (1994) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Wilkinson et al. (2013) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Wilson (1813) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Wilson (1814) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wolff et al. (2012) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Wursig & Wursig (1980) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Wüster et al. (2024) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 1 | 0.04% |
| Yuki (1993) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Zaher et al. (2012) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Zangari et al. (2006) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Zilli et al. (2005) | 2 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zimmermann & Zimmerman (1988) | 2 | 0.02% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Zuiderwijk (1990) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Zwahlen et al. (2022) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Abalos et al. (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Abalos et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Abeille & Perrin (1905) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abhaya & Probst (2009) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Abril et al. (1986) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Acerbi (1827) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Adam (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Aellen (1958) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Agassiz (1857) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Agostini et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Aguesse (1960) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Ahmadzadeh et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Albayrak et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Albesa (2010) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Albuquerque & Fernandes (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Albuquerque et al. (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Albuquerque et al. (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Alexeieff (1911) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Al-hasson & Ali (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Ali & Mendoza (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Ali et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Alkaya et al. (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Allain & Goodman (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Allioni (1785) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Almeida et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Almeida et al. (2024) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Altunişik & Kara (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Álvarez-ruiz et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Amand et al. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Amaral et al. (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Amorós (1992) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Amoureux (1959) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anaissi & Costa-campos (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anaissi & Costa-campos (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Ananie et al. (2010) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andersson (1918) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| André (1961) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andreone & Sindaco (1987) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Andrew et al. (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Andrzejowski (1832) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Angin (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Angin (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Angulo et al. (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anker & Noël (1999) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme (ICZN) (2019) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (1864) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (1999) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2001) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme (2004) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.04% | 1 | 0.04% |
| Anonyme. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | |||