Espèces endémiques
Toutes les espèces endémiques de France métropolitaine et d'outre-mer : inclut les endémiques actuelles (E) ou éteintes (Z). ATTENTION : une espèce non endémique peut apparaitre dans la liste si elle contient une sous-espèce endémique
7047 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Munzinger et al. (2016) | 5068 | 14.74% | 2497 | 11.56% | 2183 | 11.02% | 2488 | 12.1% |
Véron et al. (2021) | 4456 | 12.96% | 4356 | 20.17% | 3853 | 19.45% | 4184 | 20.34% |
Morat et al. (2012) | 3527 | 10.26% | 2489 | 11.52% | 2189 | 11.05% | 2344 | 11.4% |
Ramage (2017) | 1541 | 4.48% | 1512 | 7% | 1466 | 7.4% | 1504 | 7.31% |
Heller (1916) | 872 | 2.54% | 493 | 2.28% | 492 | 2.48% | 489 | 2.38% |
Thouvenot et al. (2011) | 706 | 2.05% | 311 | 1.44% | 287 | 1.45% | 294 | 1.43% |
Evenhuis (2018) | 556 | 1.62% | 551 | 2.55% | 550 | 2.78% | 551 | 2.68% |
Meurgey & Ramage (2020) | 534 | 1.55% | 521 | 2.41% | 513 | 2.59% | 515 | 2.5% |
Tison et al. (2014) | 492 | 1.43% | 294 | 1.36% | 247 | 1.25% | 248 | 1.21% |
Peck et al. (2014) | 414 | 1.2% | 385 | 1.78% | 385 | 1.94% | 383 | 1.86% |
Tronquet (2014) | 381 | 1.11% | 353 | 1.63% | 212 | 1.07% | 341 | 1.66% |
Meurgey (2011) | 379 | 1.1% | 263 | 1.22% | 255 | 1.29% | 258 | 1.25% |
Fauvel (1867) | 314 | 0.91% | 118 | 0.55% | 118 | 0.6% | 117 | 0.57% |
Kaszab (1982) | 303 | 0.88% | 284 | 1.31% | 271 | 1.37% | 281 | 1.37% |
Anonyme (2014) | 295 | 0.86% | 259 | 1.2% | 259 | 1.31% | 237 | 1.15% |
Holloway (1979) | 289 | 0.84% | 254 | 1.18% | 227 | 1.15% | 249 | 1.21% |
Gargominy et al. (2011) | 287 | 0.83% | 261 | 1.21% | 207 | 1.04% | 230 | 1.12% |
Clarke (1986) | 285 | 0.83% | 272 | 1.26% | 268 | 1.35% | 272 | 1.32% |
Gomy (2000) | 282 | 0.82% | 234 | 1.08% | 219 | 1.11% | 234 | 1.14% |
Martiré & Rochat (2008) | 273 | 0.79% | 234 | 1.08% | 211 | 1.07% | 218 | 1.06% |
Clarke (1971) | 269 | 0.78% | 211 | 0.98% | 211 | 1.07% | 209 | 1.02% |
Solem (1976) | 257 | 0.75% | 253 | 1.17% | 211 | 1.07% | 240 | 1.17% |
Funk et al. (2007) | 245 | 0.71% | 158 | 0.73% | 149 | 0.75% | 148 | 0.72% |
Thouvenot & Bardat (2010) | 241 | 0.7% | 143 | 0.66% | 130 | 0.66% | 129 | 0.63% |
Fauvel (1906) | 235 | 0.68% | 74 | 0.34% | 74 | 0.37% | 73 | 0.35% |
Garrett (1884) | 230 | 0.67% | 70 | 0.32% | 70 | 0.35% | 63 | 0.31% |
Falkner et al. (2002) | 223 | 0.65% | 179 | 0.83% | 141 | 0.71% | 151 | 0.73% |
Fournet (2002) | 221 | 0.64% | 181 | 0.84% | 181 | 0.91% | 157 | 0.76% |
Sudre et al. (2010) | 218 | 0.63% | 159 | 0.74% | 158 | 0.8% | 157 | 0.76% |
Perroud & Montrouzier (1864) | 217 | 0.63% | 84 | 0.39% | 84 | 0.42% | 84 | 0.41% |
Jennings et al. (2013) | 213 | 0.62% | 190 | 0.88% | 184 | 0.93% | 184 | 0.89% |
Zimmerman (1957) | 209 | 0.61% | 138 | 0.64% | 138 | 0.7% | 138 | 0.67% |
Solem (1961) | 203 | 0.59% | 134 | 0.62% | 133 | 0.67% | 129 | 0.63% |
Tavakilian & Chevillotte (2013) | 203 | 0.59% | 195 | 0.9% | 193 | 0.97% | 193 | 0.94% |
Fauvel (1904) | 196 | 0.57% | 92 | 0.43% | 92 | 0.46% | 92 | 0.45% |
Thibaud (2017) | 196 | 0.57% | 192 | 0.89% | 185 | 0.93% | 188 | 0.91% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 184 | 0.54% | 184 | 0.85% | 154 | 0.78% | 182 | 0.88% |
Kuschel (2008) | 178 | 0.52% | 164 | 0.76% | 164 | 0.83% | 164 | 0.8% |
Mary (2017) | 172 | 0.5% | 159 | 0.74% | 156 | 0.79% | 154 | 0.75% |
Pace (1991) | 171 | 0.5% | 169 | 0.78% | 165 | 0.83% | 167 | 0.81% |
Espeland et al. (2020) | 167 | 0.49% | 167 | 0.77% | 167 | 0.84% | 167 | 0.81% |
Neubert et al. (2009) | 159 | 0.46% | 25 | 0.12% | 10 | 0.05% | 21 | 0.1% |
Guillermet (2011) | 158 | 0.46% | 140 | 0.65% | 132 | 0.67% | 140 | 0.68% |
Séchet & Noël (2015) | 158 | 0.46% | 131 | 0.61% | 81 | 0.41% | 112 | 0.54% |
Fennah (1969) | 156 | 0.45% | 126 | 0.58% | 126 | 0.64% | 126 | 0.61% |
Cooke & Kondo (1961) | 153 | 0.45% | 144 | 0.67% | 84 | 0.42% | 127 | 0.62% |
Montrouzier (1861) | 151 | 0.44% | 36 | 0.17% | 36 | 0.18% | 36 | 0.18% |
Fauvel (1903) | 145 | 0.42% | 83 | 0.38% | 83 | 0.42% | 83 | 0.4% |
Uicn et al. (2012) | 145 | 0.42% | 121 | 0.56% | 101 | 0.51% | 118 | 0.57% |
Otte et al. (1987) | 143 | 0.42% | 131 | 0.61% | 131 | 0.66% | 130 | 0.63% |
Viette (1949) | 143 | 0.42% | 120 | 0.56% | 117 | 0.59% | 119 | 0.58% |
Gerlach (2016) | 140 | 0.41% | 103 | 0.48% | 78 | 0.39% | 94 | 0.46% |
Damoiseau (1966) | 136 | 0.4% | 41 | 0.19% | 41 | 0.21% | 41 | 0.2% |
Montrouzier (1861) | 132 | 0.38% | 23 | 0.11% | 23 | 0.12% | 21 | 0.1% |
Montrouzier (1860) | 129 | 0.38% | 23 | 0.11% | 23 | 0.12% | 21 | 0.1% |
Fennah (1958) | 128 | 0.37% | 128 | 0.59% | 126 | 0.64% | 127 | 0.62% |
Franz (1971) | 128 | 0.37% | 108 | 0.5% | 108 | 0.55% | 108 | 0.53% |
Platania & Gómez-Zurita (2023) | 121 | 0.35% | 119 | 0.55% | 119 | 0.6% | 119 | 0.58% |
Liebherr (2013) | 118 | 0.34% | 118 | 0.55% | 118 | 0.6% | 118 | 0.57% |
Paulay (1985) | 117 | 0.34% | 110 | 0.51% | 110 | 0.56% | 110 | 0.53% |
Glöer (2022) | 114 | 0.33% | 107 | 0.5% | 94 | 0.47% | 107 | 0.52% |
Platnick (1993) | 113 | 0.33% | 102 | 0.47% | 100 | 0.5% | 102 | 0.5% |
Baker (1938) | 111 | 0.32% | 107 | 0.5% | 82 | 0.41% | 94 | 0.46% |
Berland (1924) | 110 | 0.32% | 72 | 0.33% | 72 | 0.36% | 71 | 0.35% |
Molino et al. (2022) | 107 | 0.31% | 65 | 0.3% | 60 | 0.3% | 65 | 0.32% |
Bickel (2002) | 106 | 0.31% | 106 | 0.49% | 106 | 0.54% | 106 | 0.52% |
Fauvel (1905) | 105 | 0.31% | 84 | 0.39% | 84 | 0.42% | 79 | 0.38% |
Fricke et al. (2011) | 101 | 0.29% | 98 | 0.45% | 98 | 0.49% | 98 | 0.48% |
Fauvel (1903) | 100 | 0.29% | 68 | 0.31% | 68 | 0.34% | 66 | 0.32% |
Meyrick (1934) | 100 | 0.29% | 69 | 0.32% | 68 | 0.34% | 67 | 0.33% |
Thomson (2023) | 100 | 0.29% | 100 | 0.46% | 99 | 0.5% | 100 | 0.49% |
Gomy et al. (2016) | 96 | 0.28% | 77 | 0.36% | 74 | 0.37% | 76 | 0.37% |
Hopkins et al. (2014) | 96 | 0.28% | 90 | 0.42% | 88 | 0.44% | 89 | 0.43% |
Kuschel (1998) | 96 | 0.28% | 93 | 0.43% | 93 | 0.47% | 93 | 0.45% |
Orousset (2019) | 96 | 0.28% | 96 | 0.44% | 96 | 0.48% | 96 | 0.47% |
Gonzales et al. (2014) | 95 | 0.28% | 89 | 0.41% | 85 | 0.43% | 87 | 0.42% |
Hynes (1993) | 95 | 0.28% | 78 | 0.36% | 78 | 0.39% | 78 | 0.38% |
Muru et al. (2017) | 93 | 0.27% | 89 | 0.41% | 89 | 0.45% | 89 | 0.43% |
Pawlowska-Banasiak (2008) | 93 | 0.27% | 88 | 0.41% | 88 | 0.44% | 88 | 0.43% |
Hustache (1930) | 92 | 0.27% | 72 | 0.33% | 72 | 0.36% | 72 | 0.35% |
Verhoeff (1926) | 92 | 0.27% | 77 | 0.36% | 67 | 0.34% | 67 | 0.33% |
Zimmerman (1936) | 92 | 0.27% | 31 | 0.14% | 31 | 0.16% | 31 | 0.15% |
Fauvel (1882) | 91 | 0.26% | 56 | 0.26% | 56 | 0.28% | 56 | 0.27% |
Siu et al. (2017) | 91 | 0.26% | 90 | 0.42% | 90 | 0.45% | 90 | 0.44% |
Kaszab (1986) | 89 | 0.26% | 87 | 0.4% | 81 | 0.41% | 87 | 0.42% |
Curletti & Brûlé (2011) | 86 | 0.25% | 84 | 0.39% | 84 | 0.42% | 84 | 0.41% |
Snow (2020) | 86 | 0.25% | 84 | 0.39% | 56 | 0.28% | 78 | 0.38% |
Caporiacco (1954) | 85 | 0.25% | 67 | 0.31% | 67 | 0.34% | 67 | 0.33% |
Moore (1933) | 85 | 0.25% | 52 | 0.24% | 52 | 0.26% | 50 | 0.24% |
Bouché (1972) | 84 | 0.24% | 40 | 0.19% | 40 | 0.2% | 40 | 0.19% |
Carl (1926) | 84 | 0.24% | 68 | 0.31% | 68 | 0.34% | 68 | 0.33% |
Curletti & Brûlé (2015) | 84 | 0.24% | 82 | 0.38% | 82 | 0.41% | 82 | 0.4% |
Hayashi (1961) | 84 | 0.24% | 49 | 0.23% | 49 | 0.25% | 48 | 0.23% |
Hullé et al. (2018) | 83 | 0.24% | 68 | 0.31% | 68 | 0.34% | 58 | 0.28% |
Desutter-Grandcolas (1997) | 82 | 0.24% | 73 | 0.34% | 73 | 0.37% | 72 | 0.35% |
Florence (1997) | 81 | 0.24% | 78 | 0.36% | 75 | 0.38% | 77 | 0.37% |
Van Dyke (1937) | 81 | 0.24% | 81 | 0.38% | 81 | 0.41% | 81 | 0.39% |
Breitkreuz et al. (2016) | 79 | 0.23% | 79 | 0.37% | 79 | 0.4% | 79 | 0.38% |
Wewalka et al. (2023) | 78 | 0.23% | 78 | 0.36% | 78 | 0.39% | 78 | 0.38% |
Zimmerman (1936) | 78 | 0.23% | 78 | 0.36% | 75 | 0.38% | 75 | 0.36% |
Transactions of the entomological Society of London, 76 (2):489-521.">Meyrick (1929) | 77 | 0.22% | 54 | 0.25% | 54 | 0.27% | 54 | 0.26% |
Paulian (1991) | 77 | 0.22% | 69 | 0.32% | 66 | 0.33% | 68 | 0.33% |
Ter Steege et al. (2016) | 77 | 0.22% | 64 | 0.3% | 64 | 0.32% | 60 | 0.29% |
Razowski (2014) | 76 | 0.22% | 76 | 0.35% | 76 | 0.38% | 76 | 0.37% |
Thornton & Smithers (1974) | 76 | 0.22% | 68 | 0.31% | 68 | 0.34% | 68 | 0.33% |
Baker (1940) | 75 | 0.22% | 73 | 0.34% | 55 | 0.28% | 65 | 0.32% |
Emery (1914) | 74 | 0.22% | 29 | 0.13% | 24 | 0.12% | 26 | 0.13% |
Delfosse (2024) | 73 | 0.21% | 73 | 0.34% | 67 | 0.34% | 73 | 0.35% |
Rougemont (2018) | 73 | 0.21% | 73 | 0.34% | 73 | 0.37% | 73 | 0.35% |
Will (2020) | 72 | 0.21% | 72 | 0.33% | 72 | 0.36% | 72 | 0.35% |
Ah-Peng et al. (2010) | 71 | 0.21% | 70 | 0.32% | 57 | 0.29% | 66 | 0.32% |
Kieffer (1907-1911) | 71 | 0.21% | 33 | 0.15% | 33 | 0.17% | 33 | 0.16% |
China (1933) | 70 | 0.2% | 10 | 0.05% | 7 | 0.04% | 10 | 0.05% |
Guillermet (2006) | 70 | 0.2% | 66 | 0.31% | 58 | 0.29% | 66 | 0.32% |
Oláh & Johanson (2011) | 70 | 0.2% | 68 | 0.31% | 68 | 0.34% | 68 | 0.33% |
Rubio & Rolán (2022) | 70 | 0.2% | 70 | 0.32% | 70 | 0.35% | 70 | 0.34% |
Vedel et al. (2013) | 70 | 0.2% | 64 | 0.3% | 64 | 0.32% | 63 | 0.31% |
Bauer et al. (2022) | 69 | 0.2% | 69 | 0.32% | 69 | 0.35% | 69 | 0.34% |
O’Shea (2006) | 68 | 0.2% | 63 | 0.29% | 53 | 0.27% | 52 | 0.25% |
Defaye & Deharveng (2024) | 67 | 0.19% | 63 | 0.29% | 61 | 0.31% | 63 | 0.31% |
Poupin (2010) | 65 | 0.19% | 63 | 0.29% | 63 | 0.32% | 63 | 0.31% |
Taylor (1987) | 64 | 0.19% | 50 | 0.23% | 44 | 0.22% | 47 | 0.23% |
Distant (1920) | 62 | 0.18% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Hamilton (1981) | 62 | 0.18% | 51 | 0.24% | 51 | 0.26% | 51 | 0.25% |
Leraut (2012) | 62 | 0.18% | 60 | 0.28% | 47 | 0.24% | 25 | 0.12% |
Sartori et al. (2014) | 62 | 0.18% | 62 | 0.29% | 62 | 0.31% | 62 | 0.3% |
Fauvel (1889) | 61 | 0.18% | 27 | 0.12% | 27 | 0.14% | 27 | 0.13% |
Karg (1996) | 61 | 0.18% | 55 | 0.25% | 55 | 0.28% | 55 | 0.27% |
Wewalka et al. (2010) | 61 | 0.18% | 59 | 0.27% | 59 | 0.3% | 59 | 0.29% |
Bauer & Sadlier (2000) | 60 | 0.17% | 49 | 0.23% | 49 | 0.25% | 48 | 0.23% |
Bippus (2020) | 60 | 0.17% | 60 | 0.28% | 60 | 0.3% | 60 | 0.29% |
Matile (1993) | 60 | 0.17% | 60 | 0.28% | 60 | 0.3% | 60 | 0.29% |
Ribaut (1923) | 60 | 0.17% | 48 | 0.22% | 48 | 0.24% | 46 | 0.22% |
Chopard (1924) | 59 | 0.17% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Coote & Loeve (2003) | 59 | 0.17% | 39 | 0.18% | 39 | 0.2% | 31 | 0.15% |
Gierlasiński & Taszakowski (2024) | 59 | 0.17% | 59 | 0.27% | 59 | 0.3% | 59 | 0.29% |
Smit (2002) | 59 | 0.17% | 47 | 0.22% | 47 | 0.24% | 47 | 0.23% |
Cecalupo & Perugia (2021) | 58 | 0.17% | 58 | 0.27% | 58 | 0.29% | 58 | 0.28% |
Faille et al. (2023) | 58 | 0.17% | 58 | 0.27% | 58 | 0.29% | 42 | 0.2% |
Fauvel (1903) | 58 | 0.17% | 40 | 0.19% | 40 | 0.2% | 40 | 0.19% |
Fleutiaux & Sallé ([1890]) | 58 | 0.17% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Balukjian & Van Dam (2024) | 57 | 0.17% | 57 | 0.26% | 57 | 0.29% | 57 | 0.28% |
Burger (1995) | 57 | 0.17% | 51 | 0.24% | 51 | 0.26% | 51 | 0.25% |
Gargominy (2011-2023) | 57 | 0.17% | 57 | 0.26% | 31 | 0.16% | 57 | 0.28% |
Guillermet (2009) | 57 | 0.17% | 53 | 0.25% | 47 | 0.24% | 53 | 0.26% |
Rheinheimer (2013) | 57 | 0.17% | 56 | 0.26% | 56 | 0.28% | 56 | 0.27% |
Beenen (2017) | 56 | 0.16% | 56 | 0.26% | 56 | 0.28% | 56 | 0.27% |
Fauvel (1891) | 56 | 0.16% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Guillermet (2009) | 56 | 0.16% | 48 | 0.22% | 42 | 0.21% | 48 | 0.23% |
Haase & Bouchet (1998) | 56 | 0.16% | 51 | 0.24% | 51 | 0.26% | 51 | 0.25% |
Matile (1988) | 56 | 0.16% | 56 | 0.26% | 56 | 0.28% | 56 | 0.27% |
Transactions of the Entomological Society of London, 77: 155-169.">Meyrick (1929) | 56 | 0.16% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Decaëns et al. (2024) | 55 | 0.16% | 55 | 0.25% | 55 | 0.28% | 55 | 0.27% |
Grouvelle (1903) | 55 | 0.16% | 33 | 0.15% | 33 | 0.17% | 33 | 0.16% |
Pilsbry (1909-1910) | 55 | 0.16% | 18 | 0.08% | 16 | 0.08% | 15 | 0.07% |
Caterino (2006) | 54 | 0.16% | 54 | 0.25% | 54 | 0.27% | 54 | 0.26% |
Henderson & Breuil (2012) | 54 | 0.16% | 24 | 0.11% | 15 | 0.08% | 21 | 0.1% |
Johanson et al. (2020) | 54 | 0.16% | 54 | 0.25% | 54 | 0.27% | 54 | 0.26% |
Peck (2011) | 54 | 0.16% | 42 | 0.19% | 42 | 0.21% | 39 | 0.19% |
Rousse & Gupta (2013) | 54 | 0.16% | 54 | 0.25% | 54 | 0.27% | 54 | 0.26% |
Rousse & Villemant (2012) | 54 | 0.16% | 54 | 0.25% | 54 | 0.27% | 54 | 0.26% |
Anso et al. (2016) | 53 | 0.15% | 53 | 0.25% | 53 | 0.27% | 53 | 0.26% |
Frieser (1980) | 53 | 0.15% | 50 | 0.23% | 48 | 0.24% | 50 | 0.24% |
Molino et al. (2009) | 52 | 0.15% | 44 | 0.2% | 44 | 0.22% | 40 | 0.19% |
Monsecour & Monsecour (2018) | 52 | 0.15% | 52 | 0.24% | 52 | 0.26% | 52 | 0.25% |
Parnaudeau (2017) | 52 | 0.15% | 46 | 0.21% | 44 | 0.22% | 46 | 0.22% |
Van Dyke (1932) | 52 | 0.15% | 52 | 0.24% | 52 | 0.26% | 52 | 0.25% |
Michaelsen (1913) | 51 | 0.15% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Olah et al. (2006) | 51 | 0.15% | 0 | 0% | 0 | 0% | 0 | 0% |
Pace (2014) | 51 | 0.15% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Bescherelle (1873) | 50 | 0.15% | 9 | 0.04% | 6 | 0.03% | 8 | 0.04% |
Grouvelle & Raffray (1908) | 50 | 0.15% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Hustache (1920) | 50 | 0.15% | 44 | 0.2% | 44 | 0.22% | 44 | 0.21% |
Welter-schultes (2012) | 50 | 0.15% | 46 | 0.21% | 46 | 0.23% | 30 | 0.15% |
Bright (2019) | 49 | 0.14% | 49 | 0.23% | 49 | 0.25% | 49 | 0.24% |
Couhia & Fleurot (2016) | 49 | 0.14% | 43 | 0.2% | 42 | 0.21% | 41 | 0.2% |
Deharveng (1981) | 49 | 0.14% | 48 | 0.22% | 46 | 0.23% | 48 | 0.23% |
Delrieu-Trottin et al. (2015) | 49 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Fauvel (1903) | 49 | 0.14% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Fosberg & Sachet (1975) | 49 | 0.14% | 47 | 0.22% | 41 | 0.21% | 41 | 0.2% |
Hlaváč & Jałoszyński (2021) | 49 | 0.14% | 49 | 0.23% | 49 | 0.25% | 49 | 0.24% |
Johanson & Wells (2019) | 49 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Raven (1994) | 49 | 0.14% | 49 | 0.23% | 49 | 0.25% | 49 | 0.24% |
Wheeler (1935) | 49 | 0.14% | 21 | 0.1% | 17 | 0.09% | 19 | 0.09% |
Chassagnard & Tsacas (1997) | 48 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Evenhuis (2012) | 48 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Liebherr (2016) | 48 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Van Dyke (1932) | 48 | 0.14% | 48 | 0.22% | 48 | 0.24% | 48 | 0.23% |
Abdou & Bouchet (2000) | 47 | 0.14% | 47 | 0.22% | 45 | 0.23% | 46 | 0.22% |
Delannoye et al. (2015) | 47 | 0.14% | 32 | 0.15% | 28 | 0.14% | 32 | 0.16% |
Distant (1920) | 47 | 0.14% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Papong et al. (2014) | 47 | 0.14% | 45 | 0.21% | 45 | 0.23% | 45 | 0.22% |
Breuning (1978) | 46 | 0.13% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Grand et al. (2014) | 46 | 0.13% | 30 | 0.14% | 30 | 0.15% | 26 | 0.13% |
Hustache (1929) | 46 | 0.13% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Pace (1997) | 46 | 0.13% | 46 | 0.21% | 46 | 0.23% | 46 | 0.22% |
Paulian (1998) | 46 | 0.13% | 44 | 0.2% | 42 | 0.21% | 44 | 0.21% |
Wagner (1907-1911) | 46 | 0.13% | 13 | 0.06% | 11 | 0.06% | 11 | 0.05% |
Grand et al. (2019) | 45 | 0.13% | 29 | 0.13% | 27 | 0.14% | 29 | 0.14% |
Hullé & Vernon (2021) | 45 | 0.13% | 38 | 0.18% | 38 | 0.19% | 33 | 0.16% |
Löbl (1981) | 45 | 0.13% | 43 | 0.2% | 43 | 0.22% | 43 | 0.21% |
Constantin (2015) | 44 | 0.13% | 44 | 0.2% | 44 | 0.22% | 44 | 0.21% |
Copeland (1932) | 44 | 0.13% | 18 | 0.08% | 18 | 0.09% | 17 | 0.08% |
Massary et al. (2021) | 44 | 0.13% | 44 | 0.2% | 18 | 0.09% | 38 | 0.18% |
Montreuil & Théry (2016) | 44 | 0.13% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Pace (2014) | 44 | 0.13% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
Santamaria & Faille (2007) | 44 | 0.13% | 17 | 0.08% | 13 | 0.07% | 13 | 0.06% |
Wells & Johanson (2015) | 44 | 0.13% | 42 | 0.19% | 42 | 0.21% | 42 | 0.2% |
Abdou et al. (2004) | 43 | 0.13% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Ferrez & Royer (2021) | 43 | 0.13% | 42 | 0.19% | 42 | 0.21% | 42 | 0.2% |
Griffiths & Florens (2006) | 43 | 0.13% | 41 | 0.19% | 41 | 0.21% | 41 | 0.2% |
Raven & Churchill (1991) | 43 | 0.13% | 43 | 0.2% | 43 | 0.22% | 43 | 0.21% |
Van Zwaluwenburg (1932) | 43 | 0.13% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Bourgoin (1997) | 42 | 0.12% | 39 | 0.18% | 39 | 0.2% | 39 | 0.19% |
Fosberg (1937) | 42 | 0.12% | 38 | 0.18% | 28 | 0.14% | 37 | 0.18% |
Guenée (1862) | 42 | 0.12% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Hustache (1932) | 42 | 0.12% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Van Zwaluwenburg (1932) | 42 | 0.12% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Will (2011) | 42 | 0.12% | 42 | 0.19% | 42 | 0.21% | 42 | 0.2% |
Curletti & Brûlé (2013) | 41 | 0.12% | 40 | 0.19% | 40 | 0.2% | 40 | 0.19% |
Gâteblé et al. (2018) | 41 | 0.12% | 41 | 0.19% | 41 | 0.21% | 41 | 0.2% |
Kondo (1962) | 41 | 0.12% | 40 | 0.19% | 17 | 0.09% | 38 | 0.18% |
Montrouzier (1861) | 41 | 0.12% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Noblecourt (2016) | 41 | 0.12% | 13 | 0.06% | 12 | 0.06% | 11 | 0.05% |
Viette (1950) | 41 | 0.12% | 21 | 0.1% | 10 | 0.05% | 19 | 0.09% |
Wagner (1905) | 41 | 0.12% | 10 | 0.05% | 8 | 0.04% | 8 | 0.04% |
Berland (1933) | 40 | 0.12% | 17 | 0.08% | 17 | 0.09% | 16 | 0.08% |
Berland (1935) | 40 | 0.12% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Gould (1852) | 40 | 0.12% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Jamieson & Bennett (1979) | 40 | 0.12% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Jolivet et al. (2007) | 40 | 0.12% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Ortea (2015) | 40 | 0.12% | 40 | 0.19% | 40 | 0.2% | 40 | 0.19% |
Ward & Schefter (2000) | 40 | 0.12% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Hebard (1933) | 39 | 0.11% | 27 | 0.12% | 26 | 0.13% | 27 | 0.13% |
Hill (2013) | 39 | 0.11% | 39 | 0.18% | 39 | 0.2% | 39 | 0.19% |
Smit (2009) | 39 | 0.11% | 36 | 0.17% | 36 | 0.18% | 36 | 0.18% |
Thouvenot (2023) | 39 | 0.11% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Trojan (1991) | 39 | 0.11% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Bonfils (1969) | 38 | 0.11% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Coiffait (1980) | 38 | 0.11% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Fosberg & Sachet (1981) | 38 | 0.11% | 32 | 0.15% | 22 | 0.11% | 32 | 0.16% |
Najt & Weiner (1997) | 38 | 0.11% | 35 | 0.16% | 35 | 0.18% | 35 | 0.17% |
Pace (1987) | 38 | 0.11% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Razowski (2013) | 38 | 0.11% | 38 | 0.18% | 38 | 0.19% | 38 | 0.18% |
Brolemann (1935) | 37 | 0.11% | 32 | 0.15% | 31 | 0.16% | 31 | 0.15% |
Gasper et al. (2016) | 37 | 0.11% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Hosseini & Cassis (2019) | 37 | 0.11% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Roux (1913) | 37 | 0.11% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Samuelson (1973) | 37 | 0.11% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Schröder (1924) | 37 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Théry & Forgie (2017) | 37 | 0.11% | 37 | 0.17% | 37 | 0.19% | 37 | 0.18% |
Amati et al. (2023) | 36 | 0.1% | 36 | 0.17% | 36 | 0.18% | 36 | 0.18% |
Bechyné (1956) | 36 | 0.1% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Caziot (1903) | 36 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1862) | 36 | 0.1% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Garrett (1887) | 36 | 0.1% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Hedges & Conn (2012) | 36 | 0.1% | 20 | 0.09% | 20 | 0.1% | 16 | 0.08% |
Lorence et al. (2011) | 36 | 0.1% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Richard (1957) | 36 | 0.1% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Richling (2009) | 36 | 0.1% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Schmid (2011) | 36 | 0.1% | 36 | 0.17% | 28 | 0.14% | 34 | 0.17% |
Thiaucourt (2015) | 36 | 0.1% | 36 | 0.17% | 36 | 0.18% | 36 | 0.18% |
Uicn et al. (2015) | 36 | 0.1% | 22 | 0.1% | 20 | 0.1% | 12 | 0.06% |
Zimmerman (1936) | 36 | 0.1% | 14 | 0.06% | 12 | 0.06% | 13 | 0.06% |
Bamber (2007) | 35 | 0.1% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
D'Alessandro et al. (2016) | 35 | 0.1% | 35 | 0.16% | 35 | 0.18% | 35 | 0.17% |
Florence (1996) | 35 | 0.1% | 29 | 0.13% | 29 | 0.15% | 29 | 0.14% |
Franz (1986) | 35 | 0.1% | 31 | 0.14% | 31 | 0.16% | 31 | 0.15% |
Jolivet et al. (2013) | 35 | 0.1% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Risbec (1957) | 35 | 0.1% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Scheller (1993) | 35 | 0.1% | 35 | 0.16% | 35 | 0.18% | 35 | 0.17% |
Voisin et al. (2017) | 35 | 0.1% | 35 | 0.16% | 25 | 0.13% | 35 | 0.17% |
Dumbleton (1961) | 34 | 0.1% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Evenhuis (2013) | 34 | 0.1% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
Jacot (1934) | 34 | 0.1% | 20 | 0.09% | 12 | 0.06% | 17 | 0.08% |
Johanson (1999) | 34 | 0.1% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
Kelley (1989) | 34 | 0.1% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
Webb (2011) | 34 | 0.1% | 34 | 0.16% | 34 | 0.17% | 34 | 0.17% |
Würmli (1974) | 34 | 0.1% | 31 | 0.14% | 31 | 0.16% | 30 | 0.15% |
Bernstein et al. (2021) | 33 | 0.1% | 33 | 0.15% | 33 | 0.17% | 33 | 0.16% |
Gargominy & Fontaine (2014) | 33 | 0.1% | 33 | 0.15% | 30 | 0.15% | 32 | 0.16% |
Moore (1940) | 33 | 0.1% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Richling & Bouchet (2013) | 33 | 0.1% | 32 | 0.15% | 32 | 0.16% | 31 | 0.15% |
Vachal (1907) | 33 | 0.1% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Berland (1942) | 32 | 0.09% | 24 | 0.11% | 21 | 0.11% | 20 | 0.1% |
Borowiec et al. (2019) | 32 | 0.09% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Copeland (1938) | 32 | 0.09% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Fleutiaux (1891) | 32 | 0.09% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Florence (2004) | 32 | 0.09% | 19 | 0.09% | 18 | 0.09% | 18 | 0.09% |
Grandcolas (1997) | 32 | 0.09% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Guilbert (2002) | 32 | 0.09% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Heurtault (1986) | 32 | 0.09% | 28 | 0.13% | 28 | 0.14% | 26 | 0.13% |
Holloway & Peters (1976) | 32 | 0.09% | 25 | 0.12% | 13 | 0.07% | 23 | 0.11% |
Löbl (1973) | 32 | 0.09% | 32 | 0.15% | 32 | 0.16% | 32 | 0.16% |
Marchán et al. (2023) | 32 | 0.09% | 31 | 0.14% | 29 | 0.15% | 30 | 0.15% |
Sardet et al. (2015) | 32 | 0.09% | 29 | 0.13% | 26 | 0.13% | 24 | 0.12% |
Cecalupo & Perugia (2020) | 31 | 0.09% | 31 | 0.14% | 31 | 0.16% | 31 | 0.15% |
Craig (1997) | 31 | 0.09% | 31 | 0.14% | 31 | 0.16% | 31 | 0.15% |
Kuschel (2014) | 31 | 0.09% | 31 | 0.14% | 31 | 0.16% | 31 | 0.15% |
Lagarde (2008) | 31 | 0.09% | 30 | 0.14% | 28 | 0.14% | 30 | 0.15% |
Platania & Gómez-Zurita (2022) | 31 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Linzer Biologische Beitraege, 41(1): 767-801. ">Schöller (2009) |
31 | 0.09% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Van Duzee (1932) | 31 | 0.09% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Alexander (1978) | 30 | 0.09% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Cameron (1933) | 30 | 0.09% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Conle et al. (2020) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Hammer (1972) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Karg (1993) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Kime & Enghoff (2017) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 28 | 0.14% |
Malloch (1932) | 30 | 0.09% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Nicholson et al. (2012) | 30 | 0.09% | 19 | 0.09% | 4 | 0.02% | 17 | 0.08% |
Pace (2009) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Pelorce (2017) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Rubio & Rolán (2019) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Samuelson (2010) | 30 | 0.09% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Thouvenot (2019) | 30 | 0.09% | 17 | 0.08% | 10 | 0.05% | 17 | 0.08% |
Wanat (2001) | 30 | 0.09% | 29 | 0.13% | 29 | 0.15% | 29 | 0.14% |
Yeates (1992) | 30 | 0.09% | 30 | 0.14% | 30 | 0.15% | 30 | 0.15% |
Breuil (2002) | 29 | 0.08% | 11 | 0.05% | 4 | 0.02% | 7 | 0.03% |
Coppa & Tachet (2016) | 29 | 0.08% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Craig (1987) | 29 | 0.08% | 29 | 0.13% | 29 | 0.15% | 29 | 0.14% |
Fouts (1936) | 29 | 0.08% | 25 | 0.12% | 20 | 0.1% | 25 | 0.12% |
Graham (1987) | 29 | 0.08% | 29 | 0.13% | 29 | 0.15% | 29 | 0.14% |
Hamilton (1980) | 29 | 0.08% | 29 | 0.13% | 27 | 0.14% | 29 | 0.14% |
Pease (1869) | 29 | 0.08% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Sherff (1937) | 29 | 0.08% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Yuncker (1937) | 29 | 0.08% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Carl (1915) | 28 | 0.08% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Chalumeau & Touroult (2005) | 28 | 0.08% | 27 | 0.12% | 27 | 0.14% | 26 | 0.13% |
Fischer (2014) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Fullaway (1934) | 28 | 0.08% | 26 | 0.12% | 19 | 0.1% | 25 | 0.12% |
Garrigues & Lamy (2019) | 28 | 0.08% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Hammer (1972) | 28 | 0.08% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Hardy & Williams (2018) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Iorio et al. (2023) | 28 | 0.08% | 28 | 0.13% | 26 | 0.13% | 27 | 0.13% |
Johanson & Schefter (1999) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Leraut (2014) | 28 | 0.08% | 24 | 0.11% | 15 | 0.08% | 9 | 0.04% |
Mackerras & Rageau (1958) | 28 | 0.08% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Madl & van Achterberg (2014) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Meyrick (1926) | 28 | 0.08% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Mille et al. (2016) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Peters & Peters (2000) | 28 | 0.08% | 28 | 0.13% | 24 | 0.12% | 26 | 0.13% |
Smit et al. (2022) | 28 | 0.08% | 28 | 0.13% | 28 | 0.14% | 28 | 0.14% |
Wagner et al. (2013) | 28 | 0.08% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Balogh & Balogh (1983) | 27 | 0.08% | 27 | 0.12% | 27 | 0.14% | 27 | 0.13% |
Delfosse (2017) | 27 | 0.08% | 26 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Geraci et al. (2010) | 27 | 0.08% | 27 | 0.12% | 27 | 0.14% | 27 | 0.13% |
Grogan et al. (2016) | 27 | 0.08% | 27 | 0.12% | 27 | 0.14% | 27 | 0.13% |
Irwin et al. (2020) | 27 | 0.08% | 27 | 0.12% | 27 | 0.14% | 27 | 0.13% |
Malloch (1932) | 27 | 0.08% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Mauriès (1969) | 27 | 0.08% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Platania et al. (2019) | 27 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Racovitza (1908) | 27 | 0.08% | 6 | 0.03% | 6 | 0.03% | 0 | 0% |
Thornton (1989) | 27 | 0.08% | 24 | 0.11% | 24 | 0.12% | 23 | 0.11% |
Vives et al. (2015) | 27 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Bickel (2008) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Boeters & Falkner (2003) | 26 | 0.08% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Brotherus (1911) | 26 | 0.08% | 19 | 0.09% | 18 | 0.09% | 19 | 0.09% |
Transactions of the Entomological Society of London, 76: 469-487.">Collenette (1929) | 26 | 0.08% | 17 | 0.08% | 17 | 0.09% | 14 | 0.07% |
Evans (1974) | 26 | 0.08% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Gómez-Zurita (2022) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Karg (1993) | 26 | 0.08% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Kuschel & Chown (1995) | 26 | 0.08% | 11 | 0.05% | 11 | 0.06% | 9 | 0.04% |
Liebherr (2018) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Morrone (1998) | 26 | 0.08% | 11 | 0.05% | 11 | 0.06% | 9 | 0.04% |
Orousset (2016) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Raven (1991) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Rheinheimer (2014) | 26 | 0.08% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Taiti & Ferrara (1996) | 26 | 0.08% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Vilkamaa et al. (2012) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Will & Guéorguiev (2021) | 26 | 0.08% | 26 | 0.12% | 26 | 0.13% | 26 | 0.13% |
Beenen (2013) | 25 | 0.07% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Partula. The species inhabiting Tahiti. Carnegie Institute of Washington Publication, 228: 1-313.">Crampton (1917) | 25 | 0.07% | 6 | 0.03% | 4 | 0.02% | 5 | 0.02% |
Fauvel (1883) | 25 | 0.07% | 16 | 0.07% | 16 | 0.08% | 15 | 0.07% |
Gisin & Gama (1970) | 25 | 0.07% | 25 | 0.12% | 22 | 0.11% | 25 | 0.12% |
Kerney & Cameron (1999) | 25 | 0.07% | 22 | 0.1% | 20 | 0.1% | 9 | 0.04% |
Malloch (1933) | 25 | 0.07% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Orhant (2002) | 25 | 0.07% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Osborn (1934) | 25 | 0.07% | 24 | 0.11% | 22 | 0.11% | 24 | 0.12% |
Ross (1975) | 25 | 0.07% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Ruta & Yoshitomi (2010) | 25 | 0.07% | 25 | 0.12% | 25 | 0.13% | 25 | 0.12% |
Sellnick (1959) | 25 | 0.07% | 16 | 0.07% | 15 | 0.08% | 12 | 0.06% |
Wagner et al. (2014) | 25 | 0.07% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Allison & Holden (1971) | 24 | 0.07% | 24 | 0.11% | 18 | 0.09% | 24 | 0.12% |
Bacchet et al. (2007) | 24 | 0.07% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Baehr et al. (2013) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Breuning (1978) | 24 | 0.07% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Clastrier & Delécolle (1991) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Clastrier (1987) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Coiffait (1976) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Constantin (2012) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Coode 1982 | 24 | 0.07% | 14 | 0.06% | 11 | 0.06% | 13 | 0.06% |
Deharveng (1987) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Desutter-Grandcolas (1997) | 24 | 0.07% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Distant (1914) | 24 | 0.07% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Evenhuis (2012) | 24 | 0.07% | 24 | 0.11% | 22 | 0.11% | 24 | 0.12% |
Herbin (2016) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Kornicker (1992) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Kury et al. (2024) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Linnaeus (1758) | 24 | 0.07% | 5 | 0.02% | 5 | 0.03% | 0 | 0% |
Mckamey (2010) | 24 | 0.07% | 20 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Munzinger & Swenson (2015) | 24 | 0.07% | 22 | 0.1% | 18 | 0.09% | 20 | 0.1% |
Nielson (1975) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Paladilhe (1869) | 24 | 0.07% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Pease (1865) | 24 | 0.07% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Pease (1867) | 24 | 0.07% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Ramage et al. (2023) | 24 | 0.07% | 21 | 0.1% | 18 | 0.09% | 21 | 0.1% |
Reid & Beatson (2011) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Sartori et al. (2013) | 24 | 0.07% | 24 | 0.11% | 24 | 0.12% | 24 | 0.12% |
Beron (2022) | 23 | 0.07% | 22 | 0.1% | 20 | 0.1% | 21 | 0.1% |
Constantin (2016) | 23 | 0.07% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Gómez-Zurita & Pàmies-Harder (2022) | 23 | 0.07% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Gressitt (1960) | 23 | 0.07% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Hoch (2006) | 23 | 0.07% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Jolivet et al. (2010) | 23 | 0.07% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Lannuzel et al. (2024) | 23 | 0.07% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Lieftinck (1975) | 23 | 0.07% | 15 | 0.07% | 15 | 0.08% | 14 | 0.07% |
Polhemus (2022) | 23 | 0.07% | 23 | 0.11% | 23 | 0.12% | 23 | 0.11% |
Richoux et al. (2010) | 23 | 0.07% | 15 | 0.07% | 14 | 0.07% | 15 | 0.07% |
Subías (2009) | 23 | 0.07% | 23 | 0.11% | 22 | 0.11% | 23 | 0.11% |
Telnov (2019) | 23 | 0.07% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Valentine (1989) | 23 | 0.07% | 23 | 0.11% | 22 | 0.11% | 23 | 0.11% |
Beron (2021) | 22 | 0.06% | 22 | 0.1% | 20 | 0.1% | 21 | 0.1% |
Bigot (1992) | 22 | 0.06% | 18 | 0.08% | 17 | 0.09% | 16 | 0.08% |
Brindle (1976) | 22 | 0.06% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Fouts (1935) | 22 | 0.06% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Graham (1991) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Herbin (2015) | 22 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Kuschel (1990) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Lemagnen (2015) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 21 | 0.1% |
Malm & Johanson (2008) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Ogren et al. (1997) | 22 | 0.06% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Orhant (2003) | 22 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Pace (2014) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Pease (1871) | 22 | 0.06% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Rubio & Rolán (2021) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Samuel et al. (2019) | 22 | 0.06% | 22 | 0.1% | 22 | 0.11% | 22 | 0.11% |
Sant (2022) | 22 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Théry & Bordat (2012) | 22 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Zakardjian et al. (2023) | 22 | 0.06% | 22 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Boulard (1992) | 21 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Brotherus (1906) | 21 | 0.06% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Coineau (1968) | 21 | 0.06% | 6 | 0.03% | 3 | 0.02% | 6 | 0.03% |
Fernandez-Triana et al. (2020) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Feuillet (2009) | 21 | 0.06% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Gisin & Gama (1969) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 18 | 0.09% |
Guillermet (2004) | 21 | 0.06% | 18 | 0.08% | 10 | 0.05% | 18 | 0.09% |
Guzman et al. (2024) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Heiss (2011) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Johanson & Keijsner (2008) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Jolivet et al. (2007) | 21 | 0.06% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Kaila (2017) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Kormilev (1971) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Kudrna (2016) | 21 | 0.06% | 19 | 0.09% | 17 | 0.09% | 19 | 0.09% |
Leraut (2009) | 21 | 0.06% | 9 | 0.04% | 3 | 0.02% | 7 | 0.03% |
Löbl (1977) | 21 | 0.06% | 21 | 0.1% | 21 | 0.11% | 21 | 0.1% |
Margońska (2019) | 21 | 0.06% | 16 | 0.07% | 11 | 0.06% | 13 | 0.06% |
Nattier et al. (2015) | 21 | 0.06% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Pfeiffer (1852-1860) | 21 | 0.06% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Reeve (1849-1851) | 21 | 0.06% | 9 | 0.04% | 9 | 0.05% | 5 | 0.02% |
Tryon (1886) | 21 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Turner (1919) | 21 | 0.06% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Vitzthum (1935) | 21 | 0.06% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Yoshii (1989) | 21 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Amati et al. (2022) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Baptiste & Kimsey (2000) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Beenen (2008) | 20 | 0.06% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Bescherelle (1880) | 20 | 0.06% | 7 | 0.03% | 5 | 0.03% | 6 | 0.03% |
Bordoni (2013) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Buerki et al. (2020) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Cazanove (2022) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 19 | 0.09% |
Clastrier & Delécolle (1993) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Crampton & Cooke (1953) | 20 | 0.06% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Crampton (1956) | 20 | 0.06% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Desutter-Grandcolas et al. (2016) | 20 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Ertz et al. (2017) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Grichanov (2003) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Huang et al. (2021) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Karg (1997) | 20 | 0.06% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Le Bail et al. (2012) | 20 | 0.06% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Mauriès (1980) | 20 | 0.06% | 19 | 0.09% | 10 | 0.05% | 19 | 0.09% |
Rageau (1958) | 20 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Roux (1926) | 20 | 0.06% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Thibaud & Weiner (1997) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Vandel (1946) | 20 | 0.06% | 20 | 0.09% | 6 | 0.03% | 19 | 0.09% |
Viette (1975) | 20 | 0.06% | 20 | 0.09% | 15 | 0.08% | 19 | 0.09% |
Vilkamaa et al. (2012) | 20 | 0.06% | 20 | 0.09% | 20 | 0.1% | 20 | 0.1% |
Alexander (1957) | 19 | 0.06% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Borkent & Wirth (1997) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Coiffait (1977) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Coulomb (2000) | 19 | 0.06% | 4 | 0.02% | 2 | 0.01% | 3 | 0.01% |
Crosse (1874) | 19 | 0.06% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Desutter-Grandcolas & Robillard (2006) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 18 | 0.09% |
Desutter-Grandcolas (1997) | 19 | 0.06% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Deuve (2015) | 19 | 0.06% | 17 | 0.08% | 15 | 0.08% | 17 | 0.08% |
Fikáček (2010) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Geneva et al. (2013) | 19 | 0.06% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Grouvelle (1903) | 19 | 0.06% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Jarrige (1957) | 19 | 0.06% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
John (1977) | 19 | 0.06% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Majourau & Pillon (2020) | 19 | 0.06% | 14 | 0.06% | 13 | 0.07% | 14 | 0.07% |
Marchán et al. (2021) | 19 | 0.06% | 19 | 0.09% | 16 | 0.08% | 17 | 0.08% |
Ramage & Jouault (2020) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Reeve (1873-1874) | 19 | 0.06% | 3 | 0.01% | 3 | 0.02% | 2 | 0.01% |
Rheinheimer (2016) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Rouhan et al. (2008) | 19 | 0.06% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Sharma & Giribet (2009) | 19 | 0.06% | 19 | 0.09% | 19 | 0.1% | 19 | 0.09% |
Snow & Veldkamp (2010) | 19 | 0.06% | 13 | 0.06% | 12 | 0.06% | 10 | 0.05% |
Vandel (1947) | 19 | 0.06% | 19 | 0.09% | 13 | 0.07% | 16 | 0.08% |
Verreaux & Des Murs (1860) | 19 | 0.06% | 4 | 0.02% | 4 | 0.02% | 3 | 0.01% |
Anonyme (2016) | 18 | 0.05% | 16 | 0.07% | 14 | 0.07% | 16 | 0.08% |
Bournier & Mound (2000) | 18 | 0.05% | 18 | 0.08% | 17 | 0.09% | 18 | 0.09% |
Chopard (1915) | 18 | 0.05% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Clastrier & Delécolle (1996) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Crosse (1870) | 18 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Deharveng et al. (1997) | 18 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Deharveng (1979) | 18 | 0.05% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Fraussen & Stahlschmidt (2015) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Geoffroy & Iorio (2009) | 18 | 0.05% | 16 | 0.07% | 14 | 0.07% | 15 | 0.07% |
Gómez-Zurita & Cardoso (2014) | 18 | 0.05% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Grimpe & Hoffmann (1925) | 18 | 0.05% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Haase et al. (2005) | 18 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
James (1996) | 18 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč et al. (2020) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Lee et al. (2009) | 18 | 0.05% | 11 | 0.05% | 10 | 0.05% | 9 | 0.04% |
Liede-schumann et al. (2020) | 18 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Mazur (2016) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Mazur (2019) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Parris (2007) | 18 | 0.05% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Pease (1866) | 18 | 0.05% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Reed (1968) | 18 | 0.05% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Ribaut (1913) | 18 | 0.05% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Rousse & Braet (2012) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Schouteden (1907) | 18 | 0.05% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Snow et al. (2016) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Soldati et al. (2014) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Swenson et al. (2018) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Van Duzee (1934) | 18 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Vilvens (2023) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Vives & Sudre (2019) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Wells & Johanson (2012) | 18 | 0.05% | 18 | 0.08% | 18 | 0.09% | 18 | 0.09% |
Wenzel (1955) | 18 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Chassain & Touroult (2012) | 17 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Coulon et al. (2011) | 17 | 0.05% | 8 | 0.04% | 3 | 0.02% | 6 | 0.03% |
Evenhuis (2013) | 17 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Gómez-Zurita (2018) | 17 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Guillermet (2004) | 17 | 0.05% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Heiss (2019) | 17 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Macfie (1933) | 17 | 0.05% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Marchán et al. (2023) | 17 | 0.05% | 17 | 0.08% | 17 | 0.09% | 17 | 0.08% |
Pillon & Hequet (2019) | 17 | 0.05% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Pillon & Hequet (2021) | 17 | 0.05% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Schatz & Lowry (2018) | 17 | 0.05% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Tenorio (1976) | 17 | 0.05% | 17 | 0.08% | 10 | 0.05% | 17 | 0.08% |
Thériot (1910) | 17 | 0.05% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Wiebes (1981) | 17 | 0.05% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Balouet & Olson (1989) | 16 | 0.05% | 13 | 0.06% | 13 | 0.07% | 12 | 0.06% |
Barriera (2017) | 16 | 0.05% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Bauer et al. (2006) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Berland (1929) | 16 | 0.05% | 10 | 0.05% | 10 | 0.05% | 9 | 0.04% |
Berland (1934) | 16 | 0.05% | 10 | 0.05% | 10 | 0.05% | 8 | 0.04% |
Chassain & Touroult (2016) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Cibois et al. (2007) | 16 | 0.05% | 8 | 0.04% | 0 | 0% | 8 | 0.04% |
Cooper et al. (2013) | 16 | 0.05% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Crosse (1868) | 16 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreux & Voisin (1993) | 16 | 0.05% | 11 | 0.05% | 11 | 0.06% | 10 | 0.05% |
Dunkel (2014) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Espeland & Johanson (2007) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Fournier et al. (2018) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Gmelin (1789) | 16 | 0.05% | 1 | 0% | 1 | 0.01% | 0 | 0% |
Hausdorf (2013) | 16 | 0.05% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Holovachov (2019) | 16 | 0.05% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Jiroux (2019) | 16 | 0.05% | 16 | 0.07% | 11 | 0.06% | 16 | 0.08% |
Johnson (1994) | 16 | 0.05% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Kontschán (2013) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Kreiter et al. (2002) | 16 | 0.05% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Kulbicki (comm. pers., 2011) | 16 | 0.05% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Lapèze & Lopez-Vaamonde (2024) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Lavesque et al. (2020) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Ledoux (1991) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Lorence & Butaud (2011) | 16 | 0.05% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Lorence et al. (2007) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Matile (1991) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Menet (2009) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Patoleta et al. (2017) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Pauly et al. (2015) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Pease (1868) | 16 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters et al. (1978) | 16 | 0.05% | 16 | 0.07% | 8 | 0.04% | 12 | 0.06% |
Peters et al. (1990) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Polhemus (2010) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Shear (1993) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Taczanowski (1874) | 16 | 0.05% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Thouvenot et al. (2018) | 16 | 0.05% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Tsacas & Chassagnard (1991) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Vilkamaa et al. (2012) | 16 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vives & Sudre (2021) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Vives et al. (2011) | 16 | 0.05% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Ward (2003) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Wells et al. (2013) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Wygodzinsky (1966) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Zhang & Deharveng (2015) | 16 | 0.05% | 16 | 0.07% | 16 | 0.08% | 16 | 0.08% |
Bedos & Deharveng (1998) | 15 | 0.04% | 15 | 0.07% | 12 | 0.06% | 15 | 0.07% |
Bielawski (1973) | 15 | 0.04% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Bonfils (1969) | 15 | 0.04% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Brown (1984) | 15 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Carpenter (1935) | 15 | 0.04% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Courtial (2023) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Deharveng & Bedos (2002) | 15 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Deharveng & Najt (1988) | 15 | 0.04% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Delorme (2017) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Flechtmann & Etienne (2001) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Flechtmann & Etienne (2002) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Fournier et al. (2017) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Gompel (2021) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Guilbert (2008) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Hamilton et al. (2017) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Hlaváč et al. (2021) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Krüger et al. (2018) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Kuschel (2008) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Liebherr (1986) | 15 | 0.04% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Muratov et al. (2005) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Pauly et al. (2013) | 15 | 0.04% | 14 | 0.06% | 12 | 0.06% | 14 | 0.07% |
Pierotti (2016) | 15 | 0.04% | 12 | 0.06% | 10 | 0.05% | 11 | 0.05% |
Porch et al. (2020) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Quentin & Villiers (1979) | 15 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Reverté et al. (2023) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 9 | 0.04% |
Robillard & Desutter-Grandcolas (2008) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Rouch (1970) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Swenson & Munzinger (2016) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Uicn et al. (2017) | 15 | 0.04% | 13 | 0.06% | 13 | 0.07% | 8 | 0.04% |
Wagner & Lorence (2011) | 15 | 0.04% | 15 | 0.07% | 15 | 0.08% | 15 | 0.07% |
Zicsi & Csuzdi (1999) | 15 | 0.04% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Boeters & Falkner (2008) | 14 | 0.04% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Bonfils et al. (1994) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Botosaneanu (1994) | 14 | 0.04% | 14 | 0.06% | 11 | 0.06% | 14 | 0.07% |
Burr (1914) | 14 | 0.04% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Antenor, 3(1): 65-77.">Cerda (2016) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Chevrolat (1880) | 14 | 0.04% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Crosse (1870) | 14 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Curran (1929) | 14 | 0.04% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Darby (2020) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
De Moraes et al. (2016) | 14 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Delaunay & Melle (2013) | 14 | 0.04% | 8 | 0.04% | 5 | 0.03% | 7 | 0.03% |
Delorme (2017) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Dewynter et al. (2019) | 14 | 0.04% | 14 | 0.06% | 10 | 0.05% | 12 | 0.06% |
Fain (1974) | 14 | 0.04% | 14 | 0.06% | 10 | 0.05% | 12 | 0.06% |
Fourmanoir & Rivaton (1979) | 14 | 0.04% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Giacò et al. (2022) | 14 | 0.04% | 7 | 0.03% | 1 | 0.01% | 6 | 0.03% |
Gómez-Zurita et al. (2020) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Gomy (1976) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Graham (1984) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Guillermet (1992) | 14 | 0.04% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Guillermet (2012) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Hlaváč et al. (2006) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Keith et al. (2013) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Kondo (1968) | 14 | 0.04% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Liebherr (2012) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Liebherr (2012) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Lorence & Wagner (2011) | 14 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Montreuil & Théry (2011) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Niedbała (1998) | 14 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Oláh et al. (2022) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Pace (1984) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Paulian (1987) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Pena et al. (2010) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Pfeiffer (1850-1853) | 14 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinheimer (2019) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Russell (1958) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Smith (2008) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Thériot (1910) | 14 | 0.04% | 5 | 0.02% | 4 | 0.02% | 5 | 0.02% |
Tison et al. (2021) | 14 | 0.04% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Yoshii (1960) | 14 | 0.04% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Ythier (2018) | 14 | 0.04% | 14 | 0.06% | 14 | 0.07% | 14 | 0.07% |
Alexander (1948) | 13 | 0.04% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Balfour-Browne (1939) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Balke et al. (2014) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Barau et al. (2005) | 13 | 0.04% | 10 | 0.05% | 10 | 0.05% | 9 | 0.04% |
Bauer et al. (2012) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Berland (1934) | 13 | 0.04% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Boisduval (1833) | 13 | 0.04% | 5 | 0.02% | 5 | 0.03% | 2 | 0.01% |
Bourgeois (1884) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Bournier (2000) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Brotherus (1909) | 13 | 0.04% | 7 | 0.03% | 7 | 0.04% | 6 | 0.03% |
Cheesman (1927) | 13 | 0.04% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Damgaard & Zettel (2014) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Dierkens & Charlat (2011) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 12 | 0.06% |
Dierkens & Ramage (2016) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 11 | 0.05% |
Donskoff (1988) | 13 | 0.04% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Duval et al. (2019) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Evenhuis (2012) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Ferreira et al. (2007) | 13 | 0.04% | 7 | 0.03% | 4 | 0.02% | 7 | 0.03% |
Flechtmann & Etienne (2005) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Florence (1997) | 13 | 0.04% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Fournier et al. (2017) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Franz (1986) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Gérard et al. (2023) | 13 | 0.04% | 13 | 0.06% | 7 | 0.04% | 12 | 0.06% |
Griffini (1914) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Hagenmüller (1888) | 13 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hermans & Cribb (2021) | 13 | 0.04% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Houart et al. (2021) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
James & Gamiette (2016) | 13 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas et al. (2015) | 13 | 0.04% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Maddison (2024) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Malm & Johanson (2008) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Massary et al. (2020) | 13 | 0.04% | 12 | 0.06% | 10 | 0.05% | 10 | 0.05% |
Najt & Weiner (1991) | 13 | 0.04% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Ochs (1949) | 13 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ôhira (1971) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Pellens (2004) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Pillon et al. (2021) | 13 | 0.04% | 13 | 0.06% | 9 | 0.05% | 11 | 0.05% |
Pillon (2018) | 13 | 0.04% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Princis (1974) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Rheinheimer (2024) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Sadlier et al. (2014) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Scheerpeltz (1966) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Schmalfuss (2003) | 13 | 0.04% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Schuh (1984) | 13 | 0.04% | 13 | 0.06% | 13 | 0.07% | 13 | 0.06% |
Soldati & Touroult (2014) | 13 | 0.04% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Taczanowski (1871) | 13 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibaud & Massoud (1983) | 13 | 0.04% | 12 | 0.06% | 6 | 0.03% | 12 | 0.06% |
Wigginton (2009) | 13 | 0.04% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Wurdack et al. (1993) | 13 | 0.04% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Attié et al. (2002) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Baker (1941) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Barrabé (2014) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Barrett et al. (2021) | 12 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Boeters et al. (1989) | 12 | 0.03% | 6 | 0.03% | 6 | 0.03% | 3 | 0.01% |
Bolland (1991) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Bouchet & Abdou (2003) | 12 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Bouchet & Pointier (1998) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 10 | 0.05% |
Boulard (1980) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Boulard (1993) | 12 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Bournier & Bournier (1988) | 12 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bousquet et al. (2018) | 12 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Brechlin et al. (2016) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Broomfield (1976) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Cantero (2020) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Antenor, 4(2): 158-163, 14 fig.">Cerda (2017) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Clastrier (1985) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Clastrier (1985) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Crossay et al. (2018) | 12 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Crosse (1855) | 12 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Daugeron et al. (2024) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Deharveng (1980) | 12 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deharveng (1982) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Delfosse et al. (2019) | 12 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Delfosse (2004) | 12 | 0.03% | 10 | 0.05% | 10 | 0.05% | 9 | 0.04% |
Evenhuis (2012) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Evenhuis (2013) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Eyndhoven & Vacante (1985) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Ferragu & Richard (1992) | 12 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Feuillet (2013) | 12 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Flechtmann et al. (2000) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Fournier et al. (2017) | 12 | 0.03% | 12 | 0.06% | 9 | 0.05% | 12 | 0.06% |
Franz (1979) | 12 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Gabriac et al. (2024) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Gaimari (2004) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Gargominy (2008) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Genest (1983) | 12 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Giribet et al. (2021) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Gmelin (1788) | 12 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heppner (1995) | 12 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Hodel & Pintaud (2021) | 12 | 0.03% | 12 | 0.06% | 0 | 0% | 12 | 0.06% |
Hugel (2009) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Humala (2017) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Itrac-Bruneau & Doucet (2023) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Ivković et al. (2021) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Jałoszyński (2021) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Johanson (2003) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Jones & Cabral (1990) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Kimsey (2014) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Ledoux (2007) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Leraut (1997) | 12 | 0.03% | 2 | 0.01% | 1 | 0.01% | 1 | 0% |
Lethierry (1881) | 12 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Marquet & Roguet (2003) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
McAlpine (2007) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Monsecour & Monsecour (2015) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Montrouzier (1858) | 12 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Morat & Veillon (1985) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 5 | 0.02% |
Murphy & Matthews (1928) | 12 | 0.03% | 4 | 0.02% | 2 | 0.01% | 4 | 0.02% |
Namyatova & Cassis (2016) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Nel & Varenne (2019) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Olah & Johanson (2010) | 12 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Olah et al. (2015) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Orhant (2003) | 12 | 0.03% | 12 | 0.06% | 10 | 0.05% | 12 | 0.06% |
Pace (1984) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Patoleta (2016) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Pease (1868) | 12 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Pešić, Smit & Mary (2018) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Peters & Mary (2016) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Peters & Peters (1980) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Pignal (2023) | 12 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Pilsbry & Cooke (1915-1916) | 12 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Prout (1934) | 12 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Questel (2020) | 12 | 0.03% | 11 | 0.05% | 11 | 0.06% | 9 | 0.04% |
Robillard et al. (2010) | 12 | 0.03% | 12 | 0.06% | 10 | 0.05% | 12 | 0.06% |
Roth & Rivault (2002) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Sadlier et al. (2012) | 12 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Salazar-Vallejo (2022) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Schwenke (1999) | 12 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Silvestri (1934) | 12 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Solem (1983) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Sowerby (1842) | 12 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Sudre et al. (2021) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Taczanowski (1872) | 12 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Tanasevitch (2019) | 12 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Tarmann & Drouet (2015) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Terryn (2022) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Testo et al. (2019) | 12 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 12 | 0.03% | 8 | 0.04% | 6 | 0.03% | 7 | 0.03% |
Vaillant & Vincon (1987) | 12 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Viette (1988) | 12 | 0.03% | 10 | 0.05% | 8 | 0.04% | 10 | 0.05% |
Whittier (1976) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 10 | 0.05% |
Zimmermann et al. (2009) | 12 | 0.03% | 12 | 0.06% | 12 | 0.06% | 12 | 0.06% |
Alexander (1932) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Barabé & Gibernau (2015) | 11 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Bauer & Sadlier (1994) | 11 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Berlese (1923) | 11 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bhatti (1991) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Blackwelder (1943) | 11 | 0.03% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Cameron (1936) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Cassagnau (1964) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Caziot (1910) | 11 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Crosse (1865) | 11 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
[Denis & Schiffermüller] (1775) | 11 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt & D'hondt (2020) | 11 | 0.03% | 11 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Edwards (1932) | 11 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Fairmaire (1893) | 11 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Fikáček (2010) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Fournier (1934-1940) | 11 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy & Ripken (2006) | 11 | 0.03% | 6 | 0.03% | 4 | 0.02% | 5 | 0.02% |
Garrett (1879) | 11 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Gassies (1863) | 11 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Hlaváč (2009) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Hodel et al. (2021) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 10 | 0.05% |
Hombron & Jacquinot (1842-1853) | 11 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Jackson (1941) | 11 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Kaltenbach (1968) | 11 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Kassebeer (2000) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Kóbor (2020) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Kormilev & Froeschner (1987) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 11 | 0.03% | 7 | 0.03% | 7 | 0.04% | 3 | 0.01% |
Li (2008) | 11 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Malloch (1934) | 11 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Murdock & Smith (2003) | 11 | 0.03% | 7 | 0.03% | 6 | 0.03% | 7 | 0.03% |
Nicolas (1891) | 11 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Platnick & Forster (1993) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Rheinheimer (2012) | 11 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Rouch (1980) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Rousseau (1854) | 11 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Sadlier et al. (2009) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Shockley et al. (2009) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Stuckenberg (1970) | 11 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Subías (2004) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Talaga et al. (2015) | 11 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Thériot (1909) | 11 | 0.03% | 2 | 0.01% | 1 | 0.01% | 2 | 0.01% |
Théry (2011) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Thouvenot & Müller (2021) | 11 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Tröndlé & Boutet (2009) | 11 | 0.03% | 6 | 0.03% | 6 | 0.03% | 3 | 0.01% |
Vélain (1877) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Wanat (2008) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Ward (1984) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Ythier (2019) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Zelazny & Webb (2011) | 11 | 0.03% | 11 | 0.05% | 11 | 0.06% | 11 | 0.05% |
Albouy & Richard (2017) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 1 | 0% |
Alexander (1933) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Anonyme (2015) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Anton (1838) | 10 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1977) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bamber (2007) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Bavay (1869) | 10 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beier (1966) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bellés (1990) | 10 | 0.03% | 10 | 0.05% | 6 | 0.03% | 10 | 0.05% |
Bescherelle (1878) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Bippus (2016) | 10 | 0.03% | 10 | 0.05% | 8 | 0.04% | 10 | 0.05% |
Bolton (2000) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bouché (1970) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Boulay (1869) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Breuil (2009) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Brown (1958) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Brulin (2016) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Brulin (2018) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Bulirsch (2010) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Burch (2007) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 8 | 0.04% |
Byng et al. (2016) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Chassain (2001) | 10 | 0.03% | 10 | 0.05% | 7 | 0.04% | 8 | 0.04% |
Chevrolat (1880) | 10 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Clastrier & Wirth (1995) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Conde (1948) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Craig et al. (1995) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Curler & Jacobson (2012) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Dalens (1993) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Delorme et al. (2016) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Delrieu-Trottin (2013) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Desutter-Grandcolas (2002) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Deuss & Jourdan (2022) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
D'hondt & D'hondt (2018) | 10 | 0.03% | 10 | 0.05% | 8 | 0.04% | 10 | 0.05% |
Dujardin (1965) | 10 | 0.03% | 2 | 0.01% | 0 | 0% | 2 | 0.01% |
Evenhuis (1989) | 10 | 0.03% | 10 | 0.05% | 8 | 0.04% | 10 | 0.05% |
Evenhuis (2012) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Fage (1913) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 9 | 0.04% |
Fauvel (1877) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Fleck (2024) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Gassies (1874) | 10 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Germain et al. (2014) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Gomy (1978) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Gould (1846) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Grandcolas et al. (2014) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Gray (1992) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Guillermet (2010) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Guillermet (2011) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Haase & Zielske (2015) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Hendrian & Kondo (2007) | 10 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Hondt (1967) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Hrivniak et al. (2023) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Janák (2014) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Jennings et al. (2015) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Johanson (2017) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Johnson (1985) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Jolivet et al. (2010) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Koehler & Menzel (2013) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Komarek (2010) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Lachenaud et al. (2022) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Lacroix (1993) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Lallemand (1937) | 10 | 0.03% | 10 | 0.05% | 7 | 0.04% | 10 | 0.05% |
Leclerc (1981) | 10 | 0.03% | 10 | 0.05% | 6 | 0.03% | 8 | 0.04% |
Lemaitre (2014) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Lesson (1830-1831) | 10 | 0.03% | 5 | 0.02% | 5 | 0.03% | 3 | 0.01% |
Liebherr & Ivie (2021) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Macfie (1933) | 10 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Meuffels & Grootaert (1991) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Meuffels & Grootaert (2002) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Mille (2008) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Moubayed-Breil & Ashe (2016) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Müller et al. (2019) | 10 | 0.03% | 9 | 0.04% | 6 | 0.03% | 3 | 0.01% |
Oláh et al. (2017) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Opitz (2016) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Patoleta (2014) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Pfeiffer (1840-1850) | 10 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pignal et al. (2023) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Poussereau (2014) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Pusch (1996) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Raffray (1896) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ris (1915) | 10 | 0.03% | 5 | 0.02% | 5 | 0.03% | 4 | 0.02% |
Sadlier et al. (2002) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Difforme". Richardiana, nouvelle série, 2: 40-71.">Sambin et al. (2018) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Sanborn (2016) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Sharp (1898) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Silvestri (1915) | 10 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Siroux (2012) | 10 | 0.03% | 9 | 0.04% | 9 | 0.05% | 8 | 0.04% |
Sleumer (1938) | 10 | 0.03% | 8 | 0.04% | 6 | 0.03% | 8 | 0.04% |
Starmühlner (1970) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Tardy & Stahlschmidt (2022) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Travé (2021) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Vaillant (1983) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Verhoeff (1943) | 10 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vilkamaa et al. (2011) | 10 | 0.03% | 10 | 0.05% | 10 | 0.05% | 10 | 0.05% |
Villiers (1979) | 10 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Weygoldt (2006) | 10 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Abdou et al. (2008) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Appelhans et al. (2021) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 8 | 0.04% |
Bechyné (1957) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 8 | 0.04% |
Belles (1988) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Beron (2017) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Beruete et al. (2002) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Bippus (2018) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 8 | 0.04% |
Blair (1932) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Bonadona (1981) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Botosaneanu (2002) | 9 | 0.03% | 9 | 0.04% | 8 | 0.04% | 9 | 0.04% |
Bouché (1969) | 9 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet et al. (2008) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Boulard (1991) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Boulard (1994) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Boulard (1997) | 9 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Boulenger (1883) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Bournier (1997) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Brölemann (1900) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Bruy et al. (2023) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Carpenter (1934) | 9 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Chiron & Bellone (2005) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Cibois et al. (2004) | 9 | 0.03% | 8 | 0.04% | 6 | 0.03% | 8 | 0.04% |
Colloff (2012) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Constantin (1975) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Coquerel (1866) | 9 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Corporaal (1937) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Craig & Evenhuis (2017) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Crampton (1932) | 9 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Csuzdi (2014) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Denis (1947) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Denis (1954) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Deshayes (1863) | 9 | 0.03% | 1 | 0% | 1 | 0.01% | 0 | 0% |
Deuve (2006) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Dierkens (2021) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 7 | 0.03% |
Duhamel & King (2007) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Dupuy (1847-1852) | 9 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehanno (1993) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Evangelista et al. (2019) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Evenhuis (2004) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Faille et al. (2010) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 5 | 0.02% |
Fairmaire (1849) | 9 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Fairmaire (1858) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Fauvel (1874) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ferrer (2014) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Fitzgerald (2004) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Gaimari & Silva (2020) | 9 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Gargominy & Muratov (2012) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Germain (1931) | 9 | 0.03% | 5 | 0.02% | 5 | 0.03% | 4 | 0.02% |
Gillespie (2003) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Gillespie (2003) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Giordan & Roffaldi (1983) | 9 | 0.03% | 3 | 0.01% | 0 | 0% | 3 | 0.01% |
Giudicelli (2008) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Gómez-Zurita & Cardoso (2023) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Gómez-Zurita (2017) | 9 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Grogan et al. (2013) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Hausmann & Viidalepp (2012) | 9 | 0.03% | 7 | 0.03% | 4 | 0.02% | 6 | 0.03% |
Herbin (2022) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Johanson & Mary (2009) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Kaila (2019) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Kormilev (1970) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Lacroix (1994) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Lafranchis (2014) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 1 | 0% |
Lafranchis (2016) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 1 | 0% |
Legros et al. (2017) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Lemaire & Raffaldi (2006) | 9 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (1994) | 9 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2012) | 9 | 0.03% | 5 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Levesque & Delcroix (2018) | 9 | 0.03% | 7 | 0.03% | 5 | 0.03% | 4 | 0.02% |
Logunov (2015) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Lukoschus et al. (1979) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Malipatil & Monteith (1983) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Malloch (1932) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Maxwell & Veldkamp (1990) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Mederos et al. (2023) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Menet (2014) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Mériguet & Zagatti (2016) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 0 | 0% |
Meve et al. (2018) | 9 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Michelangeli et al. (2018) | 9 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Moquin-Tandon (1855-1856) | 9 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mordan & Tillier (1986) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Mouly et al. (2021) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Munzinger & Swenson (2009) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Murray & Clarke (1980) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Norrbom & Hancock (2004) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Ochyra et al. (2014) | 9 | 0.03% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Oláh et al. (2015) | 9 | 0.03% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Oláh et al. (2014) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Orousset (2017) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Pang et al. (2020) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Peck (2011) | 9 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Pierotti (2011) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Probst et al. (2022) | 9 | 0.03% | 8 | 0.04% | 6 | 0.03% | 6 | 0.03% |
Qiu & Bouché (1998) | 9 | 0.03% | 9 | 0.04% | 6 | 0.03% | 9 | 0.04% |
Questel & Le Quellec (2012) | 9 | 0.03% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Reeve (1842) | 9 | 0.03% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Robineau (2007) | 9 | 0.03% | 6 | 0.03% | 5 | 0.03% | 3 | 0.01% |
Rubio & Rolán (2018) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Sadlier et al. (2004) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Sambin & Chiron (2014) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Pseudepidendrum". Richardiana, nouvelle série, 2: 97-135.">Sambin et al. (2018) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Sanborn (2018) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Sanborn (2024) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Shuey (2024) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Siroux (2015) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Siroux (2018) | 9 | 0.03% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Stock & Iliffe (1995) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Sudre et al. (2022) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Swenson et al. (2021) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Taylor (2001) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Thibaud & Massoud (1979) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Tronquet (2016) | 9 | 0.03% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Vaillant (1973) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vaillant (1978) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vandrot (2018) | 9 | 0.03% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Vere Graham & Gijswit (1998) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Wanat (2013) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Yang et al. (2012) | 9 | 0.03% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Zimmerman & Perrault (1989) | 9 | 0.03% | 9 | 0.04% | 9 | 0.05% | 9 | 0.04% |
Adamski & Brown (2002) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Aguiar & Jennings (2005) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Astrongatt (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Auger et al. (2015) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Balke et al. (2017) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Ballerio (2021) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bardat et al. (2021) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 1 | 0% |
Beaver & Liu (2016) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Beier (1964) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Belfan & Conde (2016) | 8 | 0.02% | 8 | 0.04% | 2 | 0.01% | 6 | 0.03% |
Berlese (1918) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Bily (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Blair (1934) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Boeters (2000) | 8 | 0.02% | 6 | 0.03% | 4 | 0.02% | 6 | 0.03% |
Boeters (2019) | 8 | 0.02% | 5 | 0.02% | 1 | 0.01% | 4 | 0.02% |
Bordoni (2018) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bournier (1993) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Breuning (1940) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Brito et al. (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Brown & Kung (2010) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Bruce (2009) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Brûlé (2012) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Carlquist & Grant (1963) | 8 | 0.02% | 8 | 0.04% | 5 | 0.03% | 8 | 0.04% |
Casevitz-Weulersse & Galkowski (2009) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Cassis & Weirauch (2008) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Caut et al. (2013) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Cecalupo & Perugia (2023) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Chappuis & Rouch (1959) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Chassain & Touroult (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Chassain (2015) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Chevrolat (1880) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Christensen et al. (2018) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Clastrier (1993) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Constantin (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Constantin (2014) | 8 | 0.02% | 8 | 0.04% | 7 | 0.04% | 8 | 0.04% |
Cooke & Clench (1943) | 8 | 0.02% | 8 | 0.04% | 4 | 0.02% | 6 | 0.03% |
Corbera (2006) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Covain et al. (2012) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Crampton (1924) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Croat & Delannay (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Csuzdi et al. (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Cuccodoro (1998) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Curletti & Brûlé (2016) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Del et al. (1997) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Denis (1932) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 2 | 0.01% |
Drake (1890) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Drake (1957) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Dreux & Voisin (1969) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Drouët (1859) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Edwards (1933) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Enderlein (1909) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Espeland & Johanson (2008) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Euro+Med (2006) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2011) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Evenhuis (2011) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Ferragu (1979) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Flechtmann (2010) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Forcellini et al. (2012) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Gassies (1871) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Girardi (2009) | 8 | 0.02% | 6 | 0.03% | 0 | 0% | 6 | 0.03% |
Grouvelle & Raffray (1912) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guilbert (1998) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Guillermet (2011) | 8 | 0.02% | 8 | 0.04% | 6 | 0.03% | 8 | 0.04% |
Gutierrez (1979) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Hebard (1935) | 8 | 0.02% | 8 | 0.04% | 7 | 0.04% | 8 | 0.04% |
Herbin (2019) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Herbulot (1967) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Herrmann et al. (2019) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Hollis & Broomfield (1989) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Holloway & Miller (2003) | 8 | 0.02% | 8 | 0.04% | 6 | 0.03% | 6 | 0.03% |
Holttum (1977) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Iannilli & Ruffo (2007) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Iorio & Racine (2022) | 8 | 0.02% | 8 | 0.04% | 7 | 0.04% | 8 | 0.04% |
Iwan et al. (2015) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Jackson (1933) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Jeannel (1914) | 8 | 0.02% | 6 | 0.03% | 2 | 0.01% | 6 | 0.03% |
Jeannel (1919) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johanson & Ward (2001) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Johnson et al. (2000) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 6 | 0.03% |
Jourdan et al. (2023) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Knight (1983) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Kreiter et al. (2020) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Laporte de Castelnau & Brullé (1840) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Last (1980) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Ledoux & Hallé (1995) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ledoux (2004) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Léger & Duboscq (1903) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (1988) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Lourenço (1983) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Lowry & Fanini (2023) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Mauriès (1987) | 8 | 0.02% | 7 | 0.03% | 5 | 0.03% | 6 | 0.03% |
Mazur (2014) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mihara & Amaoka (2004) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Mori et al. (2002) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moulton (1939) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Murienne et al. (2008) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Murienne et al. (2009) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Niedbała & Penttinen (2007) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Niedbała (2000) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Nilsson (2007) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Oláh et al. (2020) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Parris (1997) | 8 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Patoleta & Żabka (2019) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Paudyal et al. (2018) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Paulian & Félice (1941) | 8 | 0.02% | 1 | 0% | 1 | 0.01% | 0 | 0% |
Pauly et al. (2013) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Peck & Cook (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Peters & Peters (1981) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Pfeiffer (1852) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Porat (1888) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Preston (1907) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prié (2017) | 8 | 0.02% | 8 | 0.04% | 4 | 0.02% | 4 | 0.02% |
Prószyński (2001) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Qiu & Bouché (1998) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Richard & Clark (2014) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Rodríguez-Flores et al. (2021) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Roux et al. (2019) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Rubio & Rolán (2016) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Rubio & Rolan (2018) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Rubio & Rolán (2018) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Rubio & Rolán (2020) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Sadlier et al. (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Salazar-Vallejo (2020) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Samuelson (2015) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schefter & Ward (2002) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmid (1989) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Schuster et al. (2021) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Scoble et al. (1999) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Simon (1872) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Simon (1873) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Siroux (2010) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Smith & Villemant (2017) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Solem (1964) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Spencer et al. (1992) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Steadman & Zarriello (1987) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Thériot (1907) | 8 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Thériot (1921) | 8 | 0.02% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Thibaud (1991) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Thomson (1859) | 8 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tillier & Mordan (1995) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Timberlake (1941) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Touroult (2005) | 8 | 0.02% | 7 | 0.03% | 5 | 0.03% | 6 | 0.03% |
Tronquet (2018) | 8 | 0.02% | 8 | 0.04% | 7 | 0.04% | 8 | 0.04% |
Turner (1976) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
UICN Comité français, OFB & MNHN (2021) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 0 | 0% |
Vandel (1943) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 4 | 0.02% |
Vandel (1957) | 8 | 0.02% | 8 | 0.04% | 2 | 0.01% | 8 | 0.04% |
Varenne & Nel (2016) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Vidal & Vansteene (2021) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 0 | 0% |
Vieira et al. (2019) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Viette (1959) | 8 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Vilkamaa et al. (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Vitali-di & Castri (1984) | 8 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Voisin et al. (2016) | 8 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Weiner & Najt (1991) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Wells & Johanson (2014) | 8 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Wilde & Duyfjes (2006) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Willemse (1923) | 8 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Withers & Chandler (2019) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Ythier et al. (2024) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Zhang et al. (2014) | 8 | 0.02% | 8 | 0.04% | 8 | 0.04% | 8 | 0.04% |
Antoine (1988) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Badonnel (1989) | 7 | 0.02% | 7 | 0.03% | 5 | 0.03% | 5 | 0.02% |
Balke et al. (2010) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bayly et al. (2015) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Beeson (1935) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Bell & Bell (1985) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Berlese (1910) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Bernasconi (2000) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Beron (2021) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Bertrand (1982) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Bidault et al. (2022) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Bocage (1881) | 7 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Bochaton et al. (2021) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 4 | 0.02% |
Boucher & Reyes-Castillo (1997) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Burckhardt (2009) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Chalumeau & Touroult (2004) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Chûjô (1964) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Cibois et al. (2008) | 7 | 0.02% | 3 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Cochereau (1966) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Constantin & Liberti (2006) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Crosse (1874) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deharveng & Bedos (2002) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Delorme (2018) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Dewynter et al. (2023) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 5 | 0.02% |
Donabauer (2011) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Dufay (1975) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Dujardin (1956) | 7 | 0.02% | 2 | 0.01% | 0 | 0% | 2 | 0.01% |
Evenhuis (1991) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Fauvel (1907) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Flatberg et al. (2011) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Fleutiaux (1932) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Fournier et al. (2016) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Fricke et al. (2009) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Frieser (2002) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Gierlasiński et al. (2024) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Gimmel (2011) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Gisin (1963) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Goicoechea et al. (2016) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Gómez-Zurita (2011) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Grandcolas et al. (2002) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Grouvelle (1902) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guilbert (2004) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Guilbert (2014) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Háva (2014) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Hebard (1933) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Hemsley (1885) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Herbin (2021) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Hodkinson (1983) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Houart (1991) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jackson (1938) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Jaloszynski (2018) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Jordan (1924) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Jourdan & Mille (2006) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Kóbor (2023) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Lapèze et al. (2022) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Lazell (1964) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lecoq (1990) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Legalov (2009) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Legrand (1950) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 0 | 0% |
Lescure et al. (2022) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Ślipiński (1982) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Löbl & Smetana (2010) | 7 | 0.02% | 7 | 0.03% | 0 | 0% | 7 | 0.03% |
Locard (1893) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourenço (2021) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Magniez (1978) | 7 | 0.02% | 7 | 0.03% | 4 | 0.02% | 6 | 0.03% |
Mammola & Milano (2019) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 0 | 0% |
Mayr (1933) | 7 | 0.02% | 2 | 0.01% | 1 | 0.01% | 1 | 0% |
Mazur (2017) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Mesnil (1968) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Morales-nunez et al. (2019) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Moulton & Steinweden (1932) | 7 | 0.02% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Muñoz et al. (2013) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2023) | 7 | 0.02% | 7 | 0.03% | 4 | 0.02% | 7 | 0.03% |
Nyman (1882) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra (1997) | 7 | 0.02% | 6 | 0.03% | 4 | 0.02% | 5 | 0.02% |
Olivier (1791-[1792]) | 7 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Pailler & Henze (2020) | 7 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Pfeiffer (1858) | 7 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pillon et al. (2018) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Platnick (2002) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Pointier & Marquet (1990) | 7 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Polhemus & Herring (1970) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Probst (1997) | 7 | 0.02% | 4 | 0.02% | 3 | 0.02% | 4 | 0.02% |
Ramage et al. (2018) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Rocamora (2004) | 7 | 0.02% | 5 | 0.02% | 2 | 0.01% | 4 | 0.02% |
Ruffo & Paiotta (1972) | 7 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Sambin & Chiron (2015) | 7 | 0.02% | 3 | 0.01% | 1 | 0.01% | 2 | 0.01% |
Sanchez et al. (2019) | 7 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Sánchez-Ruiz & Maréchal (2020) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Shannon & Wagner (1997) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Skejo & Deranja (2020) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Sparks et al. (2019) | 7 | 0.02% | 7 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Strohecker (1979) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Sudre & Teocchi (2000) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Szederjesi et al. (2023) | 7 | 0.02% | 4 | 0.02% | 1 | 0.01% | 3 | 0.01% |
Touroult & Poirier (2021) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Touroult (2012) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Van Zwaluwenburg (1959) | 7 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vences et al. (2001) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Vernon & Voisin (1991) | 7 | 0.02% | 4 | 0.02% | 4 | 0.02% | 3 | 0.01% |
Verwijs et al. (2019) | 7 | 0.02% | 7 | 0.03% | 4 | 0.02% | 6 | 0.03% |
Vinciguerra & Delahaye (2006) | 7 | 0.02% | 7 | 0.03% | 7 | 0.04% | 7 | 0.03% |
Waterhouse (1875) | 7 | 0.02% | 2 | 0.01% | 2 | 0.01% | 0 | 0% |
Aalbu et al. (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Acevedo-Rodríguez & Strong (2012) | 6 | 0.02% | 5 | 0.02% | 4 | 0.02% | 5 | 0.02% |
Acevedo-Rodríguez (2012) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Alexander (1932) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Andrássy (1978) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Anonyme (2015) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Apostolov (1998) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Astrongatt (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Aubert (1965) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Auger & Migeon (2014) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Averincev (1972) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Baehr & Harvey (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Balke et al. (2007) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bameul (1986) | 6 | 0.02% | 6 | 0.03% | 5 | 0.03% | 6 | 0.03% |
Barrabé & Fleurot (2021) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Beauchamp (1956) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bérenger (2001) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bernasconi (1989) | 6 | 0.02% | 4 | 0.02% | 2 | 0.01% | 4 | 0.02% |
Beron (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bescherelle (1898) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Besucht (1985) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bianchi (1952) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Bichain et al. (2007) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 1 | 0% |
Billi et al. (2011) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Boeters & Falkner (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Boeters (1981) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Bonfils (1993) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bouchet & Abdou (2001) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Boulard (2011) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bournier (1979) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Bousquet (2016) | 6 | 0.02% | 1 | 0% | 1 | 0.01% | 0 | 0% |
Boyer & Fonscolombe (1852) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Braet et al. (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Brailovsky (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Britton (1938) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Brothers (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Brown & Kung (2007) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Burks et al. (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Buyck et al. (2024) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Callot-Girardi (2015) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Carl (1909) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassagnau (1955) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Cassagnau (1959) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Castilho et al. (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Cavalcante & Johanson (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Caziot (1909) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheesman (1955) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Chevreux (1915) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1858) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1879) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Chevrolat (1880) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevrolat (1880) | 6 | 0.02% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Chown & Kuschel (1994) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Choy & Marquet (2002) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Christenhusz (2009) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 4 | 0.02% |
Clastrier (1971) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Clastrier (1985) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Clastrier (1985) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Coiffait (1969) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collin (2002) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Condé (1949) | 6 | 0.02% | 6 | 0.03% | 3 | 0.02% | 3 | 0.01% |
Constantin (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Cooke & Clench (1945) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Coppa (2017) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cowles (1994) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Craig (2004) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Crosse (1868) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dai & Jeng (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Daugeron (2000) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Dautzenberg (1923) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Davie (1992) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Degallier & Tishechkin (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deharveng & Lek (1993) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deharveng & Thibaud (1980) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deharveng (1978) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Deharveng (1982) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deharveng (1986) | 6 | 0.02% | 6 | 0.03% | 2 | 0.01% | 6 | 0.03% |
Deharveng (1988) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deknuydt et al. (2016) | 6 | 0.02% | 6 | 0.03% | 4 | 0.02% | 4 | 0.02% |
Delfosse (2003) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Delfosse (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Delorme et al. (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Denis (1947) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 4 | 0.02% |
Desutter-Grandcolas & Bland (2003) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Deuve (2006) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Deuve (2011) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Diakonoff (1977) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Dickinson et al. (2019) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Dorey et al. (2024) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Dorr & Wurdack (2020) | 6 | 0.02% | 1 | 0% | 1 | 0.01% | 0 | 0% |
Drake (1957) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Dreux & Voisin (1986) | 6 | 0.02% | 2 | 0.01% | 0 | 0% | 2 | 0.01% |
Dugdale (2005) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Duhem & Buyck (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Dumbleton (1956) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dussart (1984) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Annals & Magazine of Natural History Series 9, 20: 236-244.">Edwards (1927) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Eichhorst (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Espanol (1983) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Esper & Charpentier (1789-[1804]) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Evenhuis (2007) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Evenhuis (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Fallon (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Fauvel (1878) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Feldmann (2012) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Ferragu (1964) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ferrer (2015) | 6 | 0.02% | 6 | 0.03% | 5 | 0.03% | 6 | 0.03% |
Ferrer-Suay et al. (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Fisch-Muller et al. (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Flechtmann & Etienne (2000) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Flechtmann & Etienne (2003) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Florence (1990) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Florence (1999) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourès (1954) | 6 | 0.02% | 6 | 0.03% | 5 | 0.03% | 5 | 0.02% |
Fournier et al. (2020) | 6 | 0.02% | 6 | 0.03% | 3 | 0.02% | 3 | 0.01% |
Franz (1974) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Fricke (2000) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Gagné & Etienne (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Gargominy (2016-2021) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Gâteblé et al. (2023) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Geoffroy (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Giachino (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Gibon (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Girardi (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Gisin & Gama (1970) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Good et al. (1997) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Gorochov (2014) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1847) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourbault & Decraemer (1993) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Gouze & Deharveng (1987) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Gradstein & Lavocat Bernard (2020) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Granville & Gayot (2014) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Gray (1839) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 0 | 0% |
Grootaert et al. (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guignot (1957) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guilbert (1997) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guilbert (1999) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Guilbert (2000) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Guillermet (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
, 52: 101-125.">Gutu (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Epidendrum". Derechos Reservados, 2019. Instituto Chinoin, A.C. 136 pp.">Hágsater & Santiago [Eds] (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Haitlinger (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Hartman (1890) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Háva (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Haynes (2001) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Herbin (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Holloway (1977) | 6 | 0.02% | 6 | 0.03% | 3 | 0.02% | 3 | 0.01% |
Holmgren & Holmgren (1915) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Holttum (1973) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Hopkins & Florence (1998) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Houart & Héros (2021) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Hübner ([1790-1833]) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugel & Desutter-Grandcolas (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Hugel (2009) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Iqbal & Austin (2000) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Jałoszyński & Ślipiński (2021) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Jeannel (1938) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 0 | 0% |
Jennings et al. (2004) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Jiroux et al. (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Jolivet et al. (2008) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Jordan (1933) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kalkman & Theischinger (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kang et al. (1908) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kantor et al. (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Karg (1995) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kirchman & Steadman (2007) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kondo (1944) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Kottelat & Persat (2005) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Kurahashi & Fauran (1980) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Lawrence et al. (2007) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Layard (1878)) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Le Divelec (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Lechat & Fournier (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Leraut (1982) | 6 | 0.02% | 5 | 0.02% | 2 | 0.01% | 3 | 0.01% |
Leraut (2001) | 6 | 0.02% | 6 | 0.03% | 2 | 0.01% | 6 | 0.03% |
Liebherr (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Lindner (1859) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohmann & Taylor (2014) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Lumaret et al. (1996) | 6 | 0.02% | 3 | 0.01% | 2 | 0.01% | 3 | 0.01% |
Magniez (1968) | 6 | 0.02% | 6 | 0.03% | 0 | 0% | 6 | 0.03% |
Malm & Johanson (2007) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Marchán et al. (2022) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Marchán et al. (2023) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Martin et al. (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Martin-Sanchez et al. (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mary & Ward (2001) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Masselot & Brulin (2001) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Masson et al. (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Massoud & Thibaud (1987) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Matile (1988) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Matile-Ferrero & Balachowsky (1973) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Mauriès & Kime (1999) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Mauriès (1959) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mauriès (1961) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Mauriès (1969) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mecke (2004) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Medeiros et al. (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mertens & Wermuth (1960) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Migeon (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mikó et al. (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Modrý & Jirků (2006) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Modrý et al. (2004) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mosely (1935) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed & Langton (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed & Mary (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed & Mary (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed & Mary (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed & Mary (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed-Breil & Orsini (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Moubayed-Breil (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Mousson (1869) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Munzinger & Mcpherson (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Munzinger & Mcpherson (2021) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Namyatova & Cassis (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Nattier et al. (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Nayrolles (1995) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Nel & Varenne (2012) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Nel (1999) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Neven & Echaubard (1975) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ngoc-ho (2005) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Niemi & Behan-Pelletier (2004) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ordynets et al. (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Orousset (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Saulcy, 1862, Anillus Jacquemin du Val, 1851, et Hypotyphlus Jeannel, 1937 (Coleoptera, Carabidae). Le Coléoptériste, 18(2): 82-95.">Orousset (2015) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Ortea (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pace (2011) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Papp (1984) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Park & Will (2008) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parris (2013) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Patrick & Patrick (2012) | 6 | 0.02% | 6 | 0.03% | 4 | 0.02% | 4 | 0.02% |
Paulmier (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pešić et al. (2015) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pelorce & Horst (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Peñas & Rolán (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Penneys & Judd (2005) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1932) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pfeiffer (1843-1850) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfeiffer (1857) | 6 | 0.02% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Pic (1914) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Pierotti & Bello (2001) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pignal & Munzinger (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pignal & Queiroz (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pignal et al. (2023) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Pocock (1898) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Prié et al. (2024) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Probst (1997) | 6 | 0.02% | 2 | 0.01% | 1 | 0.01% | 2 | 0.01% |
Qiu & Bouché (1998) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ramage et al. (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Reiß (1958) | 6 | 0.02% | 2 | 0.01% | 0 | 0% | 2 | 0.01% |
Renauld (1897) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Revilliod (1914) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 3 | 0.01% |
Rheinheimer (2021) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ribaut (1920) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Ribaut (1947) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Richard (1977) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Riley (1926) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Roberts (2014) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Rodríguez-Flores et al. (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Ros-farré & Pujade-villar (2013) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Rubio & Rolán (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Sadlier et al. (1999) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Sadlier (1988) | 6 | 0.02% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Schwabe & Lozouet (2006) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Scudder (1981) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Serban et al. (1971) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Séret & Last (2003) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Sherff (1937) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Shrubovych et al. (2014) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Simon (1880) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sipahiler (1992) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Siroux (2018) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Smit et al. (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Smithers & Thornton (1974) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Souverbie (1860) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Spiessberger & Ivie (2018) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Staines & García-robledo (2014) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Stebbing (1900) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Stephensen (1935) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevens et al. (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Sudre & Vives (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Sykora (1967) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Szeptycki (1997) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Taczanowski (1873) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taiti & Ferrara (1989) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Tan (1992) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Tempère (1957) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Tenorio & Castelin (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Theowald et al. (1982) | 6 | 0.02% | 6 | 0.03% | 3 | 0.02% | 6 | 0.03% |
Thériot (1921) | 6 | 0.02% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Theuerkauf et al. (2009) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Thibaud (1993) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Thomas (1964) | 6 | 0.02% | 5 | 0.02% | 0 | 0% | 5 | 0.02% |
Tillier (1981) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 5 | 0.02% |
Timm & Brown (2014) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Touroult et al. (2022) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Touroult (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Travé (1961) | 6 | 0.02% | 6 | 0.03% | 3 | 0.02% | 3 | 0.01% |
Tristram (1879) | 6 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2019) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Uvarov (1927) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vachal (1908) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Vachon (1937) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 4 | 0.02% |
Vaillant & Withers (1993) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vaillant (1978) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Vane-Wright & De Jong (2003) | 6 | 0.02% | 5 | 0.02% | 5 | 0.03% | 0 | 0% |
Varenne & Nel (2017) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Viette (1995) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vilkamaa et al. (2012) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Villiers (1970) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vilvens (2020) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Vinson (1953) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Wagner & Lorence (2011) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Walker (1838) | 6 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Warburg (1900) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Wasshausen (2006) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Weiller (1999) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Williams & Viviani (2016) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Williams (1976) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Wittmer (1983) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Zacharda (1987) | 6 | 0.02% | 6 | 0.03% | 6 | 0.03% | 6 | 0.03% |
Zwick & Mary-Sasal (2010) | 6 | 0.02% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Allen et al. (2022) | 5 | 0.01% | 5 | 0.02% | 4 | 0.02% | 2 | 0.01% |
Ansín Agís et al. (2016) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Bulletin de l'Institut royal des sciences naturelles de Belgique, 52(23): 1-7.">Baert (1980) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Balhoff et al. (2013) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Balke (1993) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Ballantyne & Lambkin (2013) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Bamber (2004) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Barrett et al. (2019) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Bauer & Sadlier (2000) | 5 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Beatty et al. (1991) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Beauchamp (1931) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Beck (1837) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellés (1988) | 5 | 0.01% | 5 | 0.02% | 0 | 0% | 5 | 0.02% |
Bento (2023) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Berry et al. (1997) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Biffi & Constantin (2018) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Boeters & Bertrand (2001) | 5 | 0.01% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Boeters (2022) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Boisduval (1840) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkent & Dominiak (2020) | 5 | 0.01% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Bouman et al. (2022) | 5 | 0.01% | 3 | 0.01% | 3 | 0.02% | 1 | 0% |
Bour et al. (2008) | 5 | 0.01% | 3 | 0.01% | 3 | 0.02% | 2 | 0.01% |
Bourguignat (1868) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Boury-esnault et al. (1982) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Brölemann (1926) | 5 | 0.01% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Brölemann (1921) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabidoche (1968) | 5 | 0.01% | 2 | 0.01% | 1 | 0.01% | 1 | 0% |
Caceres (2002) | 5 | 0.01% | 1 | 0% | 0 | 0% | 1 | 0% |
Cameron (1933) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Carapelli et al. (2001) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Carl (1908) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Carle (1995) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Carpenter (2023) | 5 | 0.01% | 5 | 0.02% | 1 | 0.01% | 4 | 0.02% |
Cassagnau (1955) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Cassagnau (1959) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Chavez et al. (2021) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Chazeau (1991) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheesman (1953) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cherbonnier (1980) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Chevreux (1901) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Clench & Turner (1948) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Condé (1993) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Cooke (1934) | 5 | 0.01% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Costa (2011) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Crosse (1894) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cushman (1938) | 5 | 0.01% | 3 | 0.01% | 3 | 0.02% | 3 | 0.01% |
Dalens et al. (1996) | 5 | 0.01% | 4 | 0.02% | 4 | 0.02% | 4 | 0.02% |
Dalens et al. (1997) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Darlington (1934) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Davies (2002) | 5 | 0.01% | 1 | 0% | 0 | 0% | 1 | 0% |
Debach & Rosen (1976) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Defaut (2023) | 5 | 0.01% | 5 | 0.02% | 2 | 0.01% | 5 | 0.02% |
Deharveng et al. (2015) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Deharveng (1989) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Descarpentries (1979) | 5 | 0.01% | 1 | 0% | 1 | 0.01% | 1 | 0% |
Dheurle (2012) | 5 | 0.01% | 5 | 0.02% | 2 | 0.01% | 3 | 0.01% |
Dobosz (2010) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Dobrotworsky (1972) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Dole-Olivier et al. (2015) | 5 | 0.01% | 5 | 0.02% | 5 | 0.03% | 5 | 0.02% |
Draparnaud (1801) | 5 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Draparnaud (1805) |