Espèces de Guyane
Toutes les espèces de Guyane
9650 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Funk et al. (2007) | 13544 | 15.87% | 4394 | 12.76% | 4075 | 12.47% | 4079 | 12.4% |
Molino et al. (2022) | 8503 | 9.97% | 1588 | 4.61% | 1522 | 4.66% | 1504 | 4.57% |
Fournet (2002) | 5217 | 6.11% | 4076 | 11.83% | 4070 | 12.46% | 3800 | 11.55% |
Ter Steege et al. (2016) | 1888 | 2.21% | 1603 | 4.65% | 1603 | 4.91% | 1465 | 4.45% |
Molino et al. (2009) | 1502 | 1.76% | 1292 | 3.75% | 1292 | 3.95% | 1183 | 3.6% |
Uicn et al. (2017) | 1387 | 1.63% | 1316 | 3.82% | 1157 | 3.54% | 1086 | 3.3% |
Tavakilian & Chevillotte (2013) | 1185 | 1.39% | 1123 | 3.26% | 1123 | 3.44% | 1110 | 3.37% |
Lamy & Pointier (2018) | 924 | 1.08% | 824 | 2.39% | 824 | 2.52% | 824 | 2.51% |
Véron et al. (2021) | 787 | 0.92% | 752 | 2.18% | 705 | 2.16% | 743 | 2.26% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 754 | 0.88% | 496 | 1.44% | 464 | 1.42% | 488 | 1.48% |
Schaus (1905) | 654 | 0.77% | 273 | 0.79% | 273 | 0.84% | 269 | 0.82% |
Franco et al. (2019) | 653 | 0.77% | 617 | 1.79% | 604 | 1.85% | 608 | 1.85% |
Hequet & Le Corre (2010) | 648 | 0.76% | 503 | 1.46% | 498 | 1.52% | 470 | 1.43% |
Hequet et al. (2009) | 648 | 0.76% | 503 | 1.46% | 498 | 1.52% | 470 | 1.43% |
MacKee (1994) | 647 | 0.76% | 496 | 1.44% | 491 | 1.5% | 463 | 1.41% |
Meurgey & Ramage (2020) | 637 | 0.75% | 620 | 1.8% | 609 | 1.86% | 602 | 1.83% |
Remsen et al. (2013) | 599 | 0.7% | 565 | 1.64% | 565 | 1.73% | 443 | 1.35% |
Courtecuisse et al. (1996) | 585 | 0.69% | 486 | 1.41% | 480 | 1.47% | 481 | 1.46% |
Questel (2020) | 581 | 0.68% | 554 | 1.61% | 540 | 1.65% | 522 | 1.59% |
Courtecuisse (2009) | 548 | 0.64% | 89 | 0.26% | 89 | 0.27% | 87 | 0.26% |
Meurgey (2011) | 519 | 0.61% | 383 | 1.11% | 374 | 1.14% | 363 | 1.1% |
Tison et al. (2014) | 497 | 0.58% | 276 | 0.8% | 270 | 0.83% | 253 | 0.77% |
Hielkema & Hielkema (2019) | 481 | 0.56% | 471 | 1.37% | 453 | 1.39% | 464 | 1.41% |
Massemin et al. (2009) | 471 | 0.55% | 336 | 0.98% | 335 | 1.03% | 336 | 1.02% |
Delnatte & Meyer (2012) | 470 | 0.55% | 377 | 1.09% | 373 | 1.14% | 364 | 1.11% |
Hoff & Daszkiewicz (2001) | 443 | 0.52% | 273 | 0.79% | 245 | 0.75% | 210 | 0.64% |
Questel & Le Quellec (2012) | 434 | 0.51% | 394 | 1.14% | 388 | 1.19% | 368 | 1.12% |
Linnaeus (1758) | 417 | 0.49% | 51 | 0.15% | 50 | 0.15% | 37 | 0.11% |
Scoble et al. (1999) | 405 | 0.47% | 226 | 0.66% | 204 | 0.62% | 205 | 0.62% |
Meyrick (1912-1916) | 392 | 0.46% | 145 | 0.42% | 145 | 0.44% | 145 | 0.44% |
Le Bail et al. (2012) | 380 | 0.45% | 357 | 1.04% | 357 | 1.09% | 355 | 1.08% |
Poupin (2024) | 370 | 0.43% | 369 | 1.07% | 369 | 1.13% | 369 | 1.12% |
Fourdrigniez & Meyer (2008) | 367 | 0.43% | 280 | 0.81% | 272 | 0.83% | 261 | 0.79% |
Vedel et al. (2013) | 364 | 0.43% | 315 | 0.91% | 312 | 0.96% | 313 | 0.95% |
Wurdack et al. (1993) | 350 | 0.41% | 85 | 0.25% | 73 | 0.22% | 79 | 0.24% |
Remillet (1988) | 348 | 0.41% | 272 | 0.79% | 269 | 0.82% | 249 | 0.76% |
Acevedo-Rodríguez & Strong (2012) | 339 | 0.4% | 194 | 0.56% | 185 | 0.57% | 183 | 0.56% |
Heppner (1984) | 331 | 0.39% | 263 | 0.76% | 263 | 0.81% | 263 | 0.8% |
Sant (2022) | 306 | 0.36% | 295 | 0.86% | 293 | 0.9% | 278 | 0.85% |
Boggan et al. (1997) | 302 | 0.35% | 158 | 0.46% | 153 | 0.47% | 155 | 0.47% |
Pennington (1990) | 285 | 0.33% | 120 | 0.35% | 93 | 0.28% | 108 | 0.33% |
Munzinger et al. (2016) | 283 | 0.33% | 80 | 0.23% | 80 | 0.24% | 71 | 0.22% |
Hekking & Sipman (1988) | 274 | 0.32% | 210 | 0.61% | 198 | 0.61% | 204 | 0.62% |
Florschütz-de Waard et al. (2011) | 267 | 0.31% | 193 | 0.56% | 179 | 0.55% | 186 | 0.57% |
Heppner (1995) | 262 | 0.31% | 161 | 0.47% | 154 | 0.47% | 159 | 0.48% |
Swenson et al. (2023) | 255 | 0.3% | 93 | 0.27% | 92 | 0.28% | 84 | 0.26% |
Léotard & Chaline (2013) | 245 | 0.29% | 200 | 0.58% | 190 | 0.58% | 191 | 0.58% |
Görts-van Rijn (2007) | 244 | 0.29% | 67 | 0.19% | 63 | 0.19% | 63 | 0.19% |
Lombardi (2014) | 244 | 0.29% | 41 | 0.12% | 39 | 0.12% | 40 | 0.12% |
Gradstein & Ilkiu-Borges (2009) | 240 | 0.28% | 187 | 0.54% | 180 | 0.55% | 184 | 0.56% |
Jaouen et al. (2019) | 235 | 0.28% | 194 | 0.56% | 194 | 0.59% | 193 | 0.59% |
Dégallier et al. (2017) | 228 | 0.27% | 226 | 0.66% | 225 | 0.69% | 226 | 0.69% |
Faynel (2010) | 227 | 0.27% | 224 | 0.65% | 223 | 0.68% | 224 | 0.68% |
Talaga et al. (2015) | 221 | 0.26% | 193 | 0.56% | 193 | 0.59% | 193 | 0.59% |
Werkhoven (1986) | 219 | 0.26% | 114 | 0.33% | 114 | 0.35% | 113 | 0.34% |
Aublet (1775) | 217 | 0.25% | 75 | 0.22% | 74 | 0.23% | 72 | 0.22% |
Lücking (2006) | 212 | 0.25% | 202 | 0.59% | 201 | 0.62% | 201 | 0.61% |
Roux (2012) | 210 | 0.25% | 31 | 0.09% | 31 | 0.09% | 30 | 0.09% |
Wasshausen (2006) | 209 | 0.24% | 49 | 0.14% | 46 | 0.14% | 45 | 0.14% |
Lemée (1952) | 205 | 0.24% | 115 | 0.33% | 115 | 0.35% | 103 | 0.31% |
Boggan et al. (1992) | 202 | 0.24% | 114 | 0.33% | 107 | 0.33% | 107 | 0.33% |
UICN Comité français, OFB & MNHN (2021) | 202 | 0.24% | 199 | 0.58% | 199 | 0.61% | 144 | 0.44% |
Catzeflis (2012) | 200 | 0.23% | 180 | 0.52% | 180 | 0.55% | 145 | 0.44% |
Sothers et al. (2016) | 198 | 0.23% | 85 | 0.25% | 75 | 0.23% | 77 | 0.23% |
Acevedo-Rodríguez (2012) | 195 | 0.23% | 97 | 0.28% | 90 | 0.28% | 93 | 0.28% |
Vincent (2008) | 190 | 0.22% | 157 | 0.46% | 155 | 0.47% | 152 | 0.46% |
Mori et al. (2002) | 184 | 0.22% | 120 | 0.35% | 118 | 0.36% | 116 | 0.35% |
Lohmann & Taylor (2014) | 183 | 0.21% | 92 | 0.27% | 92 | 0.28% | 92 | 0.28% |
Peck et al. (2014) | 178 | 0.21% | 155 | 0.45% | 155 | 0.47% | 147 | 0.45% |
Dupuis & Perrin (2020) | 175 | 0.21% | 162 | 0.47% | 157 | 0.48% | 156 | 0.47% |
Caporiacco (1954) | 173 | 0.2% | 102 | 0.3% | 102 | 0.31% | 102 | 0.31% |
Ramage (2017) | 173 | 0.2% | 168 | 0.49% | 167 | 0.51% | 162 | 0.49% |
Curletti & Brûlé (2015) | 170 | 0.2% | 165 | 0.48% | 165 | 0.51% | 165 | 0.5% |
Morat et al. (2012) | 170 | 0.2% | 86 | 0.25% | 86 | 0.26% | 75 | 0.23% |
Anonyme (2018) | 167 | 0.2% | 141 | 0.41% | 137 | 0.42% | 141 | 0.43% |
Cremers & Boudrie (2007) | 166 | 0.19% | 81 | 0.24% | 75 | 0.23% | 75 | 0.23% |
Gonzales et al. (2014) | 166 | 0.19% | 156 | 0.45% | 150 | 0.46% | 154 | 0.47% |
Quénéhervé & Van Den Berg (2005) | 163 | 0.19% | 160 | 0.46% | 159 | 0.49% | 159 | 0.48% |
Lemée (1953) | 162 | 0.19% | 53 | 0.15% | 53 | 0.16% | 51 | 0.16% |
Felder & Rogenhofer (1864-1875) | 159 | 0.19% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Gradstein & Hekking (1989) | 158 | 0.19% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Yokoyama (2013) | 158 | 0.19% | 142 | 0.41% | 141 | 0.43% | 116 | 0.35% |
Sambin & Aucourd (2020) | 156 | 0.18% | 83 | 0.24% | 83 | 0.25% | 83 | 0.25% |
Bikaeff (2002) | 154 | 0.18% | 103 | 0.3% | 103 | 0.32% | 103 | 0.31% |
Courtecuisse (2006) | 152 | 0.18% | 118 | 0.34% | 118 | 0.36% | 118 | 0.36% |
Stace (2010) | 151 | 0.18% | 22 | 0.06% | 17 | 0.05% | 20 | 0.06% |
Chassain & Touroult (2010) | 150 | 0.18% | 142 | 0.41% | 142 | 0.43% | 142 | 0.43% |
Christenhusz (2009) | 150 | 0.18% | 105 | 0.3% | 102 | 0.31% | 96 | 0.29% |
Paton et al. (2019) | 148 | 0.17% | 9 | 0.03% | 7 | 0.02% | 7 | 0.02% |
Levesque & Delcroix (2018) | 147 | 0.17% | 143 | 0.42% | 124 | 0.38% | 130 | 0.4% |
Elix & McCarthy (1998) | 146 | 0.17% | 113 | 0.33% | 110 | 0.34% | 100 | 0.3% |
Morat & Veillon (1985) | 146 | 0.17% | 114 | 0.33% | 113 | 0.35% | 101 | 0.31% |
Borowiec & Moragues (2005) | 143 | 0.17% | 142 | 0.41% | 139 | 0.43% | 139 | 0.42% |
Zoosystema, 42(7) : 105-114.">Pocco & Cigliano (2020) | 142 | 0.17% | 141 | 0.41% | 128 | 0.39% | 140 | 0.43% |
Ponchel (2011) | 141 | 0.17% | 120 | 0.35% | 118 | 0.36% | 113 | 0.34% |
Thouvenot et al. (2011) | 141 | 0.17% | 36 | 0.1% | 36 | 0.11% | 33 | 0.1% |
Jourdan & Mille (2006) | 130 | 0.15% | 121 | 0.35% | 121 | 0.37% | 118 | 0.36% |
Lemée (1955) | 129 | 0.15% | 58 | 0.17% | 58 | 0.18% | 55 | 0.17% |
Floch & Abonnenc (1952) | 128 | 0.15% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Peck (2011) | 128 | 0.15% | 111 | 0.32% | 106 | 0.32% | 111 | 0.34% |
Bouchon-Navaro et al. (2005) | 126 | 0.15% | 109 | 0.32% | 109 | 0.33% | 108 | 0.33% |
Sambin (2020) | 126 | 0.15% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Chiron & Bellone (2005) | 125 | 0.15% | 69 | 0.2% | 69 | 0.21% | 68 | 0.21% |
Cook & Scoble (1995) | 125 | 0.15% | 36 | 0.1% | 35 | 0.11% | 35 | 0.11% |
Curletti & Brûlé (2013) | 125 | 0.15% | 113 | 0.33% | 113 | 0.35% | 113 | 0.34% |
Lévêque (2015) | 125 | 0.15% | 33 | 0.1% | 32 | 0.1% | 33 | 0.1% |
Kuijt (2007) | 124 | 0.15% | 26 | 0.08% | 26 | 0.08% | 26 | 0.08% |
Courtecuisse & Welti (2013) | 123 | 0.14% | 84 | 0.24% | 82 | 0.25% | 79 | 0.24% |
Barabé & Gibernau (2015) | 121 | 0.14% | 105 | 0.3% | 96 | 0.29% | 97 | 0.29% |
Bricaud (2007) | 121 | 0.14% | 91 | 0.26% | 89 | 0.27% | 88 | 0.27% |
Courtial (2023) | 121 | 0.14% | 118 | 0.34% | 118 | 0.36% | 118 | 0.36% |
Pitkin (2002) | 120 | 0.14% | 80 | 0.23% | 73 | 0.22% | 74 | 0.22% |
Berg (1992) | 119 | 0.14% | 71 | 0.21% | 60 | 0.18% | 60 | 0.18% |
Bernard (2015) | 119 | 0.14% | 78 | 0.23% | 77 | 0.24% | 74 | 0.22% |
Skog & Feuillet (2008) | 119 | 0.14% | 33 | 0.1% | 33 | 0.1% | 33 | 0.1% |
Guenée (1852) | 117 | 0.14% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Kuijt (2003) | 117 | 0.14% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Lescure et al. (2022) | 117 | 0.14% | 115 | 0.33% | 115 | 0.35% | 115 | 0.35% |
Maas et al. (2015) | 113 | 0.13% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Poupin & Corbari (2016) | 112 | 0.13% | 98 | 0.28% | 98 | 0.3% | 98 | 0.3% |
Feuillet (2009) | 111 | 0.13% | 80 | 0.23% | 77 | 0.24% | 75 | 0.23% |
Lescure & Marty (2000) | 107 | 0.13% | 48 | 0.14% | 48 | 0.15% | 48 | 0.15% |
Allorge-Boiteau (2015) | 106 | 0.12% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Bardat et al. (2021) | 104 | 0.12% | 22 | 0.06% | 22 | 0.07% | 21 | 0.06% |
Bénéluz (2021) | 103 | 0.12% | 101 | 0.29% | 72 | 0.22% | 100 | 0.3% |
Barneby & Grimes (1996) | 102 | 0.12% | 6 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Matile-Ferrero & Etienne (2006) | 100 | 0.12% | 93 | 0.27% | 91 | 0.28% | 91 | 0.28% |
Corbari et al. (2015) | 99 | 0.12% | 80 | 0.23% | 80 | 0.24% | 80 | 0.24% |
Michelangeli et al. (2018) | 99 | 0.12% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Peck (2011) | 99 | 0.12% | 82 | 0.24% | 78 | 0.24% | 79 | 0.24% |
Sleumer (1980) | 99 | 0.12% | 16 | 0.05% | 10 | 0.03% | 14 | 0.04% |
Meyrick (1916-1923) | 98 | 0.11% | 43 | 0.12% | 43 | 0.13% | 43 | 0.13% |
Minot (2016) | 98 | 0.11% | 92 | 0.27% | 92 | 0.28% | 85 | 0.26% |
Øvstedal (2010) | 98 | 0.11% | 80 | 0.23% | 80 | 0.24% | 76 | 0.23% |
Clements (2012) | 97 | 0.11% | 84 | 0.24% | 74 | 0.23% | 73 | 0.22% |
Deknuydt et al. (2016) | 97 | 0.11% | 92 | 0.27% | 92 | 0.28% | 91 | 0.28% |
Lapèze (2021) | 97 | 0.11% | 97 | 0.28% | 97 | 0.3% | 97 | 0.29% |
Granville & Gayot (2014) | 96 | 0.11% | 90 | 0.26% | 77 | 0.24% | 80 | 0.24% |
Feldmann (2012) | 93 | 0.11% | 81 | 0.24% | 81 | 0.25% | 81 | 0.25% |
Curletti & Brûlé (2011) | 91 | 0.11% | 84 | 0.24% | 84 | 0.26% | 84 | 0.26% |
Lapèze & Dalens (2021) | 91 | 0.11% | 91 | 0.26% | 91 | 0.28% | 91 | 0.28% |
Tostain et al. (2013) | 91 | 0.11% | 76 | 0.22% | 74 | 0.23% | 61 | 0.19% |
Cremers & Hoff (1992) | 90 | 0.11% | 35 | 0.1% | 35 | 0.11% | 35 | 0.11% |
Freire-Fierro (2002) | 90 | 0.11% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Brévignon & Benmesbah (2012) | 89 | 0.1% | 46 | 0.13% | 42 | 0.13% | 39 | 0.12% |
Laporte de Castelnau & Brullé (1840) | 89 | 0.1% | 32 | 0.09% | 32 | 0.1% | 30 | 0.09% |
Zuloaga et al. (2011) | 89 | 0.1% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Boullet et al. (2018) | 88 | 0.1% | 78 | 0.23% | 77 | 0.24% | 72 | 0.22% |
Buyck (2013) | 88 | 0.1% | 74 | 0.21% | 73 | 0.22% | 73 | 0.22% |
Constantin (2021) | 88 | 0.1% | 87 | 0.25% | 80 | 0.24% | 87 | 0.26% |
Struwe et al. (2014) | 88 | 0.1% | 28 | 0.08% | 26 | 0.08% | 27 | 0.08% |
Ramage et al. (2023) | 87 | 0.1% | 87 | 0.25% | 87 | 0.27% | 87 | 0.26% |
Spinola (1841) | 87 | 0.1% | 30 | 0.09% | 30 | 0.09% | 28 | 0.09% |
Uicn et al. (2015) | 87 | 0.1% | 85 | 0.25% | 85 | 0.26% | 61 | 0.19% |
Costa et al. (2008) | 86 | 0.1% | 81 | 0.24% | 81 | 0.25% | 81 | 0.25% |
Fabricius (1801) | 85 | 0.1% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Florence (2004) | 85 | 0.1% | 73 | 0.21% | 70 | 0.21% | 72 | 0.22% |
Vieira et al. (2019) | 85 | 0.1% | 75 | 0.22% | 75 | 0.23% | 75 | 0.23% |
Judziewicz (1990) | 84 | 0.1% | 52 | 0.15% | 52 | 0.16% | 52 | 0.16% |
Pennington & Wise (2017) | 84 | 0.1% | 30 | 0.09% | 27 | 0.08% | 29 | 0.09% |
Rheinheimer (2021) | 84 | 0.1% | 82 | 0.24% | 82 | 0.25% | 82 | 0.25% |
Degallier et al. (2018) | 82 | 0.1% | 82 | 0.24% | 82 | 0.25% | 82 | 0.25% |
Pace (2015) | 82 | 0.1% | 82 | 0.24% | 82 | 0.25% | 82 | 0.25% |
Yvinec (2010) | 82 | 0.1% | 82 | 0.24% | 81 | 0.25% | 82 | 0.25% |
Fournier et al. (2024) | 81 | 0.09% | 81 | 0.24% | 81 | 0.25% | 81 | 0.25% |
Mori et al. (1997) | 81 | 0.09% | 46 | 0.13% | 44 | 0.13% | 45 | 0.14% |
Soula (2010) | 81 | 0.09% | 72 | 0.21% | 65 | 0.2% | 67 | 0.2% |
Spinola (1840) | 81 | 0.09% | 51 | 0.15% | 51 | 0.16% | 51 | 0.16% |
Bricaud (2009) | 78 | 0.09% | 73 | 0.21% | 73 | 0.22% | 73 | 0.22% |
Krolow et al. (2017) | 78 | 0.09% | 77 | 0.22% | 76 | 0.23% | 77 | 0.23% |
Poupin (2010) | 78 | 0.09% | 68 | 0.2% | 68 | 0.21% | 68 | 0.21% |
Schuiteman & Chase (2015) | 78 | 0.09% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Cramer ([1780]-1782) | 77 | 0.09% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Rinaldi (2016) | 76 | 0.09% | 76 | 0.22% | 76 | 0.23% | 44 | 0.13% |
Meurgey & Picard (2011) | 75 | 0.09% | 69 | 0.2% | 69 | 0.21% | 69 | 0.21% |
Øllgaard et al. (2020) | 75 | 0.09% | 11 | 0.03% | 8 | 0.02% | 9 | 0.03% |
Poole (1989) | 75 | 0.09% | 70 | 0.2% | 70 | 0.21% | 70 | 0.21% |
Dewynter & Claessens (2020) | 74 | 0.09% | 72 | 0.21% | 70 | 0.21% | 56 | 0.17% |
Fraga & Carvalho (2021) | 74 | 0.09% | 71 | 0.21% | 71 | 0.22% | 58 | 0.18% |
Fricke et al. (2011) | 74 | 0.09% | 71 | 0.21% | 71 | 0.22% | 68 | 0.21% |
Morales (1999) | 74 | 0.09% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Oláh & Johanson (2011) | 74 | 0.09% | 70 | 0.2% | 70 | 0.21% | 70 | 0.21% |
Pennington & Biggs (2016) | 74 | 0.09% | 41 | 0.12% | 34 | 0.1% | 35 | 0.11% |
Busck (1911) | 73 | 0.09% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Caterino & Tishechkin (2013) | 73 | 0.09% | 70 | 0.2% | 70 | 0.21% | 70 | 0.21% |
Prance et al. (2007) | 73 | 0.09% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Cramer ([1779]) | 72 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 72 | 0.08% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Delannoye et al. (2015) | 71 | 0.08% | 43 | 0.12% | 43 | 0.13% | 43 | 0.13% |
Dewynter (2018) | 71 | 0.08% | 67 | 0.19% | 67 | 0.21% | 67 | 0.2% |
Durand (2019) | 70 | 0.08% | 70 | 0.2% | 70 | 0.21% | 70 | 0.21% |
Dyar (1905) | 70 | 0.08% | 53 | 0.15% | 53 | 0.16% | 53 | 0.16% |
Tricart & Foubert (2000) | 70 | 0.08% | 49 | 0.14% | 49 | 0.15% | 49 | 0.15% |
Dickinson & Remsen (2013) | 69 | 0.08% | 55 | 0.16% | 44 | 0.13% | 49 | 0.15% |
Thouvenot & Bardat (2010) | 69 | 0.08% | 17 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Anonyme (2014) | 68 | 0.08% | 58 | 0.17% | 58 | 0.18% | 56 | 0.17% |
Bechyné, B. S. de. 1976. Phytophages (Coléoptères) récoltés en Guyane Française par la mission du Muséum national d'Histoire naturelle. Annales de la Société Entomologique de France, 12(4): 527-556.">Bechyné (1976) | 68 | 0.08% | 64 | 0.19% | 48 | 0.15% | 64 | 0.19% |
Bouchon-Navaro & Louis (1986) | 68 | 0.08% | 60 | 0.17% | 60 | 0.18% | 60 | 0.18% |
Dégallier et al. (2021) | 68 | 0.08% | 68 | 0.2% | 68 | 0.21% | 68 | 0.21% |
Diaz & Cuzange (2009) | 68 | 0.08% | 59 | 0.17% | 59 | 0.18% | 56 | 0.17% |
Luer (2006) | 68 | 0.08% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Smith (1997) | 67 | 0.08% | 57 | 0.17% | 51 | 0.16% | 57 | 0.17% |
Corriol & Roy (2021) | 66 | 0.08% | 58 | 0.17% | 56 | 0.17% | 58 | 0.18% |
Gmelin (1789) | 66 | 0.08% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Pace (2014) | 66 | 0.08% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Brévignon & Gallard (1997) | 65 | 0.08% | 53 | 0.15% | 36 | 0.11% | 52 | 0.16% |
Gargominy (2016-2021) | 65 | 0.08% | 58 | 0.17% | 56 | 0.17% | 58 | 0.18% |
Dognin (1908) | 64 | 0.08% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Fleutiaux (1930) | 64 | 0.08% | 55 | 0.16% | 55 | 0.17% | 55 | 0.17% |
Lévêque (2014) | 64 | 0.08% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Berg et al. (1990) | 63 | 0.07% | 24 | 0.07% | 17 | 0.05% | 18 | 0.05% |
Berg (1972) | 63 | 0.07% | 10 | 0.03% | 6 | 0.02% | 7 | 0.02% |
Dewynter (2020) | 62 | 0.07% | 57 | 0.17% | 57 | 0.17% | 30 | 0.09% |
Korotkova et al. (2017) | 62 | 0.07% | 8 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Brown (1958) | 61 | 0.07% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Conle et al. (2020) | 61 | 0.07% | 54 | 0.16% | 54 | 0.17% | 54 | 0.16% |
Sanborn (2011) | 61 | 0.07% | 50 | 0.15% | 50 | 0.15% | 50 | 0.15% |
Soares et al. (2021) | 61 | 0.07% | 28 | 0.08% | 24 | 0.07% | 18 | 0.05% |
Clavier et al. (2019) | 60 | 0.07% | 60 | 0.17% | 60 | 0.18% | 59 | 0.18% |
Clavier et al. (2021) | 60 | 0.07% | 60 | 0.17% | 60 | 0.18% | 59 | 0.18% |
Cramer ([1777]) | 60 | 0.07% | 1 | 0% | 1 | 0% | 1 | 0% |
Jourdan (2020) | 60 | 0.07% | 59 | 0.17% | 57 | 0.17% | 56 | 0.17% |
Berry et al. (2003) | 59 | 0.07% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Caterino & Tishechkin (2013) | 59 | 0.07% | 59 | 0.17% | 59 | 0.18% | 59 | 0.18% |
Berndt (2013) | 58 | 0.07% | 58 | 0.17% | 58 | 0.18% | 58 | 0.18% |
Decaëns et al. (2024) | 58 | 0.07% | 58 | 0.17% | 58 | 0.18% | 58 | 0.18% |
Galkowski (2016) | 58 | 0.07% | 56 | 0.16% | 56 | 0.17% | 56 | 0.17% |
Lévêque (2009) | 58 | 0.07% | 57 | 0.17% | 53 | 0.16% | 53 | 0.16% |
Pauly et al. (2013) | 58 | 0.07% | 54 | 0.16% | 54 | 0.17% | 54 | 0.16% |
Borchsenius et al. (2012) | 57 | 0.07% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Borgato et al. (2020) | 57 | 0.07% | 54 | 0.16% | 54 | 0.17% | 53 | 0.16% |
Carzon et al. (2016) | 57 | 0.07% | 57 | 0.17% | 57 | 0.17% | 33 | 0.1% |
Estrade et al. (2016) | 57 | 0.07% | 57 | 0.17% | 57 | 0.17% | 33 | 0.1% |
Graciolli et al. (2019) | 57 | 0.07% | 57 | 0.17% | 56 | 0.17% | 56 | 0.17% |
Taczanowski (1874) | 57 | 0.07% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Belfan & Conde (2016) | 56 | 0.07% | 53 | 0.15% | 50 | 0.15% | 42 | 0.13% |
Constantin (2015) | 56 | 0.07% | 54 | 0.16% | 54 | 0.17% | 54 | 0.16% |
Taczanowski (1872) | 56 | 0.07% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Wilmot-Dear & Friis (1996) | 56 | 0.07% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Aptroot & Lücking (2016) | 55 | 0.06% | 53 | 0.15% | 53 | 0.16% | 53 | 0.16% |
European Nucleotide Archive (2019) | 55 | 0.06% | 48 | 0.14% | 48 | 0.15% | 48 | 0.15% |
Queiroz & Snak (2020) | 55 | 0.06% | 25 | 0.07% | 19 | 0.06% | 20 | 0.06% |
Strong (2006) | 55 | 0.06% | 42 | 0.12% | 40 | 0.12% | 40 | 0.12% |
Aymard & Kelloff (2016) | 54 | 0.06% | 26 | 0.08% | 20 | 0.06% | 21 | 0.06% |
Berg (2001) | 54 | 0.06% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Boom et al. (2011) | 54 | 0.06% | 48 | 0.14% | 48 | 0.15% | 43 | 0.13% |
Bousquet (2016) | 54 | 0.06% | 1 | 0% | 1 | 0% | 1 | 0% |
Chérot & Carpintero (2016) | 54 | 0.06% | 53 | 0.15% | 53 | 0.16% | 53 | 0.16% |
Hausherr et al. (2024) | 54 | 0.06% | 54 | 0.16% | 54 | 0.17% | 54 | 0.16% |
Heller (1895) | 54 | 0.06% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
IUCN (2013) | 54 | 0.06% | 50 | 0.15% | 50 | 0.15% | 45 | 0.14% |
Li et al. (2019) | 54 | 0.06% | 51 | 0.15% | 48 | 0.15% | 39 | 0.12% |
Mora & Clark (2016) | 54 | 0.06% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Fricke et al. (2009) | 53 | 0.06% | 48 | 0.14% | 48 | 0.15% | 45 | 0.14% |
Gallard & Wood (2017) | 53 | 0.06% | 36 | 0.1% | 18 | 0.06% | 36 | 0.11% |
Haxaire & Rasplus (1986) | 53 | 0.06% | 47 | 0.14% | 38 | 0.12% | 42 | 0.13% |
Lupoli (2023) | 53 | 0.06% | 51 | 0.15% | 51 | 0.16% | 51 | 0.16% |
Siu et al. (2017) | 53 | 0.06% | 49 | 0.14% | 49 | 0.15% | 46 | 0.14% |
Boisduval & Guénée ([1874]) | 52 | 0.06% | 6 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Cremers & Hoff (1997) | 52 | 0.06% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Fabricius (1803) | 52 | 0.06% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Guenée ([1858]) | 52 | 0.06% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Pace (2014) | 52 | 0.06% | 40 | 0.12% | 40 | 0.12% | 40 | 0.12% |
Talaga & Duchemin (2023) | 52 | 0.06% | 48 | 0.14% | 48 | 0.15% | 48 | 0.15% |
Cramer ([1775-1776]) | 51 | 0.06% | 2 | 0.01% | 2 | 0.01% | 0 | 0% |
Cremers & Hoff (1994) | 51 | 0.06% | 17 | 0.05% | 14 | 0.04% | 15 | 0.05% |
Etcheberry & Abraham (2009) | 51 | 0.06% | 44 | 0.13% | 44 | 0.13% | 34 | 0.1% |
Fonseca et al. (2017) | 51 | 0.06% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Pitkin (1993) | 51 | 0.06% | 44 | 0.13% | 40 | 0.12% | 40 | 0.12% |
Rheinheimer (2015) | 51 | 0.06% | 51 | 0.15% | 51 | 0.16% | 51 | 0.16% |
Thomson (2023) | 51 | 0.06% | 51 | 0.15% | 51 | 0.16% | 51 | 0.16% |
Zhang et al. (2022) | 51 | 0.06% | 43 | 0.12% | 42 | 0.13% | 29 | 0.09% |
Béarez et al. (2017) | 50 | 0.06% | 50 | 0.15% | 50 | 0.15% | 47 | 0.14% |
Rheinheimer (2018) | 50 | 0.06% | 49 | 0.14% | 49 | 0.15% | 49 | 0.15% |
Rudge (1805) | 50 | 0.06% | 8 | 0.02% | 8 | 0.02% | 6 | 0.02% |
Betz (1980) | 49 | 0.06% | 39 | 0.11% | 39 | 0.12% | 38 | 0.12% |
Dognin (1910) | 49 | 0.06% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Duss (1903) | 49 | 0.06% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Fouquet et al. (2019) | 49 | 0.06% | 48 | 0.14% | 48 | 0.15% | 48 | 0.15% |
Girod & Matzke (2020) | 49 | 0.06% | 49 | 0.14% | 49 | 0.15% | 49 | 0.15% |
Horak & Mouchacca (1998) | 49 | 0.06% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Rochas et al. (2022) | 49 | 0.06% | 43 | 0.12% | 43 | 0.13% | 43 | 0.13% |
Taczanowski (1873) | 49 | 0.06% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Thiaucourt (2015) | 49 | 0.06% | 49 | 0.14% | 49 | 0.15% | 49 | 0.15% |
Constantin (2017) | 48 | 0.06% | 46 | 0.13% | 46 | 0.14% | 46 | 0.14% |
Espeland et al. (2023) | 48 | 0.06% | 39 | 0.11% | 39 | 0.12% | 38 | 0.12% |
Webster & Armbruster (1991) | 48 | 0.06% | 15 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Austin (1973) | 47 | 0.06% | 17 | 0.05% | 13 | 0.04% | 14 | 0.04% |
Belokobylskij et al. (2017) | 47 | 0.06% | 44 | 0.13% | 44 | 0.13% | 44 | 0.13% |
Brugneaux & Pérès (2006) | 47 | 0.06% | 41 | 0.12% | 41 | 0.13% | 41 | 0.12% |
Gmelin (1788) | 47 | 0.06% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Guenée (1854) | 47 | 0.06% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Kuijt (2009) | 47 | 0.06% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Olivier (1791-[1792]) | 47 | 0.06% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Caires (2012) | 46 | 0.05% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Gibeaux (1983) | 46 | 0.05% | 46 | 0.13% | 46 | 0.14% | 46 | 0.14% |
Morvan & Roguet (2013) | 46 | 0.05% | 38 | 0.11% | 38 | 0.12% | 38 | 0.12% |
Rogers & Appan (1973) | 46 | 0.05% | 2 | 0.01% | 2 | 0.01% | 1 | 0% |
Schaus (1928) | 46 | 0.05% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Shelley & Lehtinen (1999) | 46 | 0.05% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Zaremski et al. (2014) | 46 | 0.05% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Almeida & van den Berg (2021) | 45 | 0.05% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Bauters et al. (2019) | 45 | 0.05% | 5 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Campos & Desutter-Grandcolas (2020) | 45 | 0.05% | 45 | 0.13% | 41 | 0.13% | 45 | 0.14% |
Dognin (1908) | 45 | 0.05% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Florence (1997) | 45 | 0.05% | 29 | 0.08% | 28 | 0.09% | 27 | 0.08% |
Gargominy et al. (1996) | 45 | 0.05% | 36 | 0.1% | 36 | 0.11% | 35 | 0.11% |
Guenée (1852) | 45 | 0.05% | 31 | 0.09% | 31 | 0.09% | 31 | 0.09% |
Haxaire & Rasplus (1987) | 45 | 0.05% | 42 | 0.12% | 35 | 0.11% | 36 | 0.11% |
Jaffe & Lattke (1994) | 45 | 0.05% | 42 | 0.12% | 42 | 0.13% | 42 | 0.13% |
Maas (1985) | 45 | 0.05% | 19 | 0.06% | 17 | 0.05% | 17 | 0.05% |
Monniot (2016) | 45 | 0.05% | 40 | 0.12% | 40 | 0.12% | 40 | 0.12% |
Olivier (1792) | 45 | 0.05% | 1 | 0% | 1 | 0% | 0 | 0% |
Rheinheimer (2014) | 45 | 0.05% | 45 | 0.13% | 45 | 0.14% | 45 | 0.14% |
Rheinheimer (2016) | 45 | 0.05% | 45 | 0.13% | 45 | 0.14% | 45 | 0.14% |
Schneider & Zizka (2016) | 45 | 0.05% | 19 | 0.06% | 16 | 0.05% | 17 | 0.05% |
Smit et al. (2022) | 45 | 0.05% | 42 | 0.12% | 42 | 0.13% | 42 | 0.13% |
Van Dijk et al. (2012) | 45 | 0.05% | 32 | 0.09% | 28 | 0.09% | 28 | 0.09% |
Daly & Fine (2018) | 44 | 0.05% | 33 | 0.1% | 33 | 0.1% | 27 | 0.08% |
Heppner (1982) | 44 | 0.05% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Taczanowski (1871) | 44 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tavakilian & Peñaherrera-Leiva (2003) | 44 | 0.05% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Blanco et al. (2007) | 43 | 0.05% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Bogarín et al. (2014) | 43 | 0.05% | 1 | 0% | 1 | 0% | 1 | 0% |
Constantin (2016) | 43 | 0.05% | 35 | 0.1% | 35 | 0.11% | 35 | 0.11% |
Damián et al. (2018) | 43 | 0.05% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Guimarães et al. (2019) | 43 | 0.05% | 11 | 0.03% | 7 | 0.02% | 9 | 0.03% |
Hall (2018) | 43 | 0.05% | 16 | 0.05% | 14 | 0.04% | 15 | 0.05% |
Hollowell et al. (2001) | 43 | 0.05% | 19 | 0.06% | 18 | 0.06% | 18 | 0.05% |
Louis et al. (1992) | 43 | 0.05% | 34 | 0.1% | 34 | 0.1% | 33 | 0.1% |
Braet (2006) | 42 | 0.05% | 36 | 0.1% | 36 | 0.11% | 36 | 0.11% |
Curletti & Brûlé (2017) | 42 | 0.05% | 42 | 0.12% | 42 | 0.13% | 42 | 0.13% |
Ferrufino-acosta (2010) | 42 | 0.05% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Lehnert (2016) | 42 | 0.05% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Pelorce (2017) | 42 | 0.05% | 41 | 0.12% | 41 | 0.13% | 41 | 0.12% |
Szlachetko et al. (2012) | 42 | 0.05% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
van der Werff (2008) | 41 | 0.05% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Amarante (2002) | 40 | 0.05% | 40 | 0.12% | 37 | 0.11% | 40 | 0.12% |
Chen et al. (2017) | 40 | 0.05% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Dewynter (2021) | 40 | 0.05% | 38 | 0.11% | 38 | 0.12% | 38 | 0.12% |
Fournier et al. (2016) | 40 | 0.05% | 38 | 0.11% | 38 | 0.12% | 38 | 0.12% |
Zornia". Webbia, 16(1): 1-141.">Mohlenbrock (1961) | 40 | 0.05% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Rheinheimer (2016) | 40 | 0.05% | 40 | 0.12% | 40 | 0.12% | 40 | 0.12% |
Tavakilian & Néouze (2013) | 40 | 0.05% | 31 | 0.09% | 31 | 0.09% | 31 | 0.09% |
Fabricius (1787) | 39 | 0.05% | 1 | 0% | 1 | 0% | 0 | 0% |
Forero (1983) | 39 | 0.05% | 19 | 0.06% | 13 | 0.04% | 15 | 0.05% |
Hewitson (1867-1871) | 39 | 0.05% | 16 | 0.05% | 14 | 0.04% | 9 | 0.03% |
Judd et al. (2018) | 39 | 0.05% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Leponce et al. (2019) | 39 | 0.05% | 36 | 0.1% | 35 | 0.11% | 36 | 0.11% |
Linnaeus (1753) | 39 | 0.05% | 24 | 0.07% | 24 | 0.07% | 22 | 0.07% |
Poole (1987) | 39 | 0.05% | 39 | 0.11% | 39 | 0.12% | 39 | 0.12% |
Berg & Roselli (2005) | 38 | 0.04% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Desutter-Grandcolas (1992) | 38 | 0.04% | 38 | 0.11% | 34 | 0.1% | 36 | 0.11% |
Fabricius (1775) | 38 | 0.04% | 1 | 0% | 1 | 0% | 1 | 0% |
Carmen Coscaron (1983) | 37 | 0.04% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Carnevali et al. (2003) | 37 | 0.04% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Cremers & Hoff (1998) | 37 | 0.04% | 16 | 0.05% | 12 | 0.04% | 12 | 0.04% |
Curletti & Brûlé (2014) | 37 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Ferlay et al. (2023) | 37 | 0.04% | 37 | 0.11% | 37 | 0.11% | 34 | 0.1% |
Gomy (2000) | 37 | 0.04% | 32 | 0.09% | 32 | 0.1% | 32 | 0.1% |
Meyer et al. (2006) | 37 | 0.04% | 22 | 0.06% | 21 | 0.06% | 20 | 0.06% |
Mitchell (1997) | 37 | 0.04% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Roy (2019) | 37 | 0.04% | 31 | 0.09% | 31 | 0.09% | 31 | 0.09% |
Senevet & Abonnenc (1939) | 37 | 0.04% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Wilson (2003) | 37 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Batista et al. (2011) | 36 | 0.04% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Berry et al. (1995) | 36 | 0.04% | 14 | 0.04% | 14 | 0.04% | 13 | 0.04% |
Delprete & Kirkbride (2015) | 36 | 0.04% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Fortuna-Perez & Azevedo Tozzi (2011) | 36 | 0.04% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Fryxell (1999) | 36 | 0.04% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Henderson & Breuil (2012) | 36 | 0.04% | 28 | 0.08% | 24 | 0.07% | 22 | 0.07% |
Lavergne (2011) | 36 | 0.04% | 28 | 0.08% | 25 | 0.08% | 26 | 0.08% |
Maas et al. (2007) | 36 | 0.04% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Néouze & Tavakilian (2005) | 36 | 0.04% | 36 | 0.1% | 36 | 0.11% | 36 | 0.11% |
Ormerod (2013) | 36 | 0.04% | 1 | 0% | 1 | 0% | 1 | 0% |
Streito et al. (2007) | 36 | 0.04% | 36 | 0.1% | 36 | 0.11% | 36 | 0.11% |
Constantin (2014) | 35 | 0.04% | 35 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Fabricius (1787) | 35 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraldo-Cañas (2012) | 35 | 0.04% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Kaastra (1982) | 35 | 0.04% | 10 | 0.03% | 4 | 0.01% | 5 | 0.02% |
Kubitzki (1970) | 35 | 0.04% | 10 | 0.03% | 6 | 0.02% | 7 | 0.02% |
Olmi & Virla (2014) | 35 | 0.04% | 33 | 0.1% | 33 | 0.1% | 33 | 0.1% |
Reichardt (1995) | 35 | 0.04% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Royen (1951) | 35 | 0.04% | 25 | 0.07% | 23 | 0.07% | 24 | 0.07% |
Vincent & Laguerre (2014) | 35 | 0.04% | 27 | 0.08% | 23 | 0.07% | 27 | 0.08% |
Camacho et al. (2022) | 34 | 0.04% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Christenhusz et al. (2018) | 34 | 0.04% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Espírito Santo et al. (2019) | 34 | 0.04% | 8 | 0.02% | 8 | 0.02% | 6 | 0.02% |
Pace (2015) | 34 | 0.04% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Pace (2015) | 34 | 0.04% | 34 | 0.1% | 34 | 0.1% | 34 | 0.1% |
Poupin (2018) | 34 | 0.04% | 31 | 0.09% | 31 | 0.09% | 31 | 0.09% |
Schintlmeister (2013) | 34 | 0.04% | 22 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Wickel & Jamon (2010) | 34 | 0.04% | 32 | 0.09% | 32 | 0.1% | 31 | 0.09% |
Ythier (2018) | 34 | 0.04% | 34 | 0.1% | 33 | 0.1% | 34 | 0.1% |
Berry et al. (1998) | 33 | 0.04% | 13 | 0.04% | 10 | 0.03% | 11 | 0.03% |
Bricaud (2008) | 33 | 0.04% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Cabral (2016) | 33 | 0.04% | 10 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Dejean (1825) | 33 | 0.04% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Delprete (2015) | 33 | 0.04% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Echternacht (2012) | 33 | 0.04% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Fortuna-Perez (2009) | 33 | 0.04% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Germar (1824) | 33 | 0.04% | 1 | 0% | 1 | 0% | 1 | 0% |
Hewitson (1871) | 33 | 0.04% | 19 | 0.06% | 19 | 0.06% | 16 | 0.05% |
Michelangeli (2005) | 33 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown & Kung (2010) | 32 | 0.04% | 32 | 0.09% | 32 | 0.1% | 32 | 0.1% |
Buck (2003) | 32 | 0.04% | 20 | 0.06% | 14 | 0.04% | 20 | 0.06% |
Delprete & Kirkbride (2016) | 32 | 0.04% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Desutter-Grandcolas & Faberon (2020) | 32 | 0.04% | 28 | 0.08% | 27 | 0.08% | 27 | 0.08% |
Dewynter et al. (2022) | 32 | 0.04% | 32 | 0.09% | 32 | 0.1% | 12 | 0.04% |
Feuillet (2014) | 32 | 0.04% | 30 | 0.09% | 28 | 0.09% | 29 | 0.09% |
Herbin (2016) | 32 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Johnston (1935) | 32 | 0.04% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Kallunki & Pirani (1998) | 32 | 0.04% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Linnaeus (1766) | 32 | 0.04% | 6 | 0.02% | 5 | 0.02% | 5 | 0.02% |
Néouze & Tavakilian (2010) | 32 | 0.04% | 32 | 0.09% | 32 | 0.1% | 32 | 0.1% |
Ortuño & Borsch (2020) | 32 | 0.04% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Paulay & Brown (2019) | 32 | 0.04% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Prance (2009) | 32 | 0.04% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Questel (2016) | 32 | 0.04% | 30 | 0.09% | 30 | 0.09% | 29 | 0.09% |
Shockley et al. (2009) | 32 | 0.04% | 32 | 0.09% | 31 | 0.09% | 32 | 0.1% |
Vayssières et al. (2001) | 32 | 0.04% | 28 | 0.08% | 28 | 0.09% | 26 | 0.08% |
Zuloaga (2022) | 32 | 0.04% | 3 | 0.01% | 2 | 0.01% | 1 | 0% |
Brullé (1846) | 31 | 0.04% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Cowan & Lindeman (1989) | 31 | 0.04% | 9 | 0.03% | 8 | 0.02% | 8 | 0.02% |
Delfosse (2017) | 31 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Ensaf et al. (2004) | 31 | 0.04% | 27 | 0.08% | 27 | 0.08% | 27 | 0.08% |
Feuillet & Poncy (1998) | 31 | 0.04% | 14 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Fine et al. (2014) | 31 | 0.04% | 26 | 0.08% | 24 | 0.07% | 20 | 0.06% |
Fournier & Lechat (2015) | 31 | 0.04% | 31 | 0.09% | 31 | 0.09% | 31 | 0.09% |
Hopkins (1915) | 31 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavocat Bernard (2018) | 31 | 0.04% | 26 | 0.08% | 25 | 0.08% | 26 | 0.08% |
Mille et al. (2016) | 31 | 0.04% | 31 | 0.09% | 31 | 0.09% | 29 | 0.09% |
Morley (1976) | 31 | 0.04% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Pace (2014) | 31 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Peñaherrera-Leiva & Tavakilian (2004) | 31 | 0.04% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Philbrick et al. (2016) | 31 | 0.04% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Prance & da Silva (1973) | 31 | 0.04% | 5 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Rudd (1965) | 31 | 0.04% | 14 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Uicn et al. (2020) | 31 | 0.04% | 31 | 0.09% | 31 | 0.09% | 24 | 0.07% |
Wigginton (2009) | 31 | 0.04% | 21 | 0.06% | 21 | 0.06% | 19 | 0.06% |
Collette & Nauen (1983) | 30 | 0.04% | 30 | 0.09% | 26 | 0.08% | 30 | 0.09% |
Constantin (2018) | 30 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
De Geer (1773) | 30 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Degallier et al. (2010) | 30 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Duranton (2004) | 30 | 0.04% | 29 | 0.08% | 27 | 0.08% | 26 | 0.08% |
Fournier et al. (2020) | 30 | 0.04% | 30 | 0.09% | 28 | 0.09% | 28 | 0.09% |
Germain et al. (2014) | 30 | 0.04% | 30 | 0.09% | 30 | 0.09% | 28 | 0.09% |
Gillespie & Armbruster (1997) | 30 | 0.04% | 22 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Grandcolas (1994) | 30 | 0.04% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Kaehler et al. (2019) | 30 | 0.04% | 27 | 0.08% | 27 | 0.08% | 27 | 0.08% |
Khan (2007) | 30 | 0.04% | 11 | 0.03% | 6 | 0.02% | 9 | 0.03% |
Lachenaud & Delprete (2022) | 30 | 0.04% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Lacomme (2013) | 30 | 0.04% | 26 | 0.08% | 13 | 0.04% | 21 | 0.06% |
Linnaeus (1753) | 30 | 0.04% | 22 | 0.06% | 22 | 0.07% | 21 | 0.06% |
Oláh & Oláh (2017) | 30 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
O’Shea (2006) | 30 | 0.04% | 22 | 0.06% | 19 | 0.06% | 22 | 0.07% |
Poulain et al. (2011) | 30 | 0.04% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Smidt et al. (2021) | 30 | 0.04% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Sothers et al. (2014) | 30 | 0.04% | 25 | 0.07% | 21 | 0.06% | 21 | 0.06% |
Taylor et al. (2020) | 30 | 0.04% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Toulgoët (1987) | 30 | 0.04% | 30 | 0.09% | 30 | 0.09% | 30 | 0.09% |
Bauters et al. (2016) | 29 | 0.03% | 24 | 0.07% | 24 | 0.07% | 21 | 0.06% |
Bellone & Chiron (2003) | 29 | 0.03% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Boulard (1980) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Carvalho (1997) | 29 | 0.03% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Fiedler (1940) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Gabriac et al. (2024) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Harvey (1992) | 29 | 0.03% | 1 | 0% | 1 | 0% | 1 | 0% |
Hovestadt & Neckheim (2020) | 29 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Lapèze & Lopez-Vaamonde (2024) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Leblanc (2014) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Martiré & Rochat (2008) | 29 | 0.03% | 22 | 0.06% | 22 | 0.07% | 21 | 0.06% |
Pastore & Abbott (2012) | 29 | 0.03% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Poupin et al. (1999) | 29 | 0.03% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Poupin (1994) | 29 | 0.03% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Rheinheimer (2019) | 29 | 0.03% | 29 | 0.08% | 29 | 0.09% | 29 | 0.09% |
Rousseau (2010) | 29 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Rudd (1987) | 29 | 0.03% | 10 | 0.03% | 4 | 0.01% | 7 | 0.02% |
Souza & Giulietti (2009) | 29 | 0.03% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Taylor & Gereau (2013) | 29 | 0.03% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Allem (1994) | 28 | 0.03% | 3 | 0.01% | 1 | 0% | 2 | 0.01% |
Andersson (1981) | 28 | 0.03% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Caterino & Tishechkin (2020) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Colijn et al. (2020) | 28 | 0.03% | 25 | 0.07% | 25 | 0.08% | 20 | 0.06% |
Croat & Delannay (2017) | 28 | 0.03% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Dognin (1911) | 28 | 0.03% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Dognin (1912) | 28 | 0.03% | 13 | 0.04% | 12 | 0.04% | 13 | 0.04% |
Dognin (1914) | 28 | 0.03% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Dyar (1914) | 28 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Eggers (1933) | 28 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Fischer et al. (2013) | 28 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gmelin (1791) | 28 | 0.03% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Guzman et al. (2024) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Heiss & Moragues (2009) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Krapovickas (2003) | 28 | 0.03% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Lapèze (2019) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Lepeletier (1841) | 28 | 0.03% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Moore et al. (2018) | 28 | 0.03% | 26 | 0.08% | 23 | 0.07% | 26 | 0.08% |
Moraes (2012) | 28 | 0.03% | 6 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Olmi & Guglielmino (2016) | 28 | 0.03% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Rheinheimer (2017) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Ruzzier et al. (2023) | 28 | 0.03% | 28 | 0.08% | 28 | 0.09% | 28 | 0.09% |
Welker et al. (2020) | 28 | 0.03% | 26 | 0.08% | 26 | 0.08% | 23 | 0.07% |
Bergroth (1914) | 27 | 0.03% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Boom (1984) | 27 | 0.03% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Bouchet & Pointier (1998) | 27 | 0.03% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Cavalcante (1983) | 27 | 0.03% | 5 | 0.01% | 2 | 0.01% | 4 | 0.01% |
Defaye & Dussart (1988) | 27 | 0.03% | 26 | 0.08% | 26 | 0.08% | 26 | 0.08% |
Etienne (2005) | 27 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Gardner et al. (2021) | 27 | 0.03% | 13 | 0.04% | 13 | 0.04% | 12 | 0.04% |
Handlos (1975) | 27 | 0.03% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Henderson (2011) | 27 | 0.03% | 6 | 0.02% | 4 | 0.01% | 4 | 0.01% |
Larridon et al. (2011) | 27 | 0.03% | 1 | 0% | 1 | 0% | 1 | 0% |
Maas (1985) | 27 | 0.03% | 9 | 0.03% | 7 | 0.02% | 8 | 0.02% |
Maurin et al. (2017) | 27 | 0.03% | 10 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Morales (2009) | 27 | 0.03% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Rothschild (1917) | 27 | 0.03% | 4 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Rudd (1977) | 27 | 0.03% | 6 | 0.02% | 5 | 0.02% | 4 | 0.01% |
Sanborn (2019) | 27 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Santos-Silva et al. (2020) | 27 | 0.03% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Silva et al. (2015) | 27 | 0.03% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Vincent & Laguerre (2013) | 27 | 0.03% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Wood et al. (2020) | 27 | 0.03% | 24 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Berry et al. (1999) | 26 | 0.03% | 16 | 0.05% | 11 | 0.03% | 10 | 0.03% |
Dauphin (2003) | 26 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuve (2011) | 26 | 0.03% | 26 | 0.08% | 26 | 0.08% | 26 | 0.08% |
Dewynter (2021) | 26 | 0.03% | 26 | 0.08% | 25 | 0.08% | 21 | 0.06% |
Galea et al. (2021) | 26 | 0.03% | 26 | 0.08% | 26 | 0.08% | 26 | 0.08% |
Germain (2007) | 26 | 0.03% | 26 | 0.08% | 26 | 0.08% | 24 | 0.07% |
Guglielmone et al. (2023) | 26 | 0.03% | 26 | 0.08% | 26 | 0.08% | 26 | 0.08% |
Hovenkamp & Miyamoto (2005) | 26 | 0.03% | 5 | 0.01% | 5 | 0.02% | 4 | 0.01% |
Kükenthal (1936) | 26 | 0.03% | 4 | 0.01% | 1 | 0% | 3 | 0.01% |
Léotard et al. (2017) | 26 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Lima et al. (2022) | 26 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Lohez (2015) | 26 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Luer (1997) | 26 | 0.03% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Mitchell & Daly (2015) | 26 | 0.03% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Poey (1858-61) | 26 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocha et al. (2017) | 26 | 0.03% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Rohwer (1993) | 26 | 0.03% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Smith & Downs (1979) | 26 | 0.03% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Taylor (1989) | 26 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Tronquet (2014) | 26 | 0.03% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Vayssières et al. (2013) | 26 | 0.03% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Walker (1865-[1866]) | 26 | 0.03% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Alves et al. (2015) | 25 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Bourguignon et al. (2016) | 25 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Camargo & Azevedo Tozzi (2014) | 25 | 0.03% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Costea et al. (2001) | 25 | 0.03% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Foldi & Germain (2018) | 25 | 0.03% | 25 | 0.07% | 25 | 0.08% | 23 | 0.07% |
Herbin (2015) | 25 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Lowe et al. (2007) | 25 | 0.03% | 20 | 0.06% | 18 | 0.06% | 19 | 0.06% |
Madriñán (2004) | 25 | 0.03% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Mangabeira (1942) | 25 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyrick (1923-1930) | 25 | 0.03% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 25 | 0.03% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Paulmier (1996) | 25 | 0.03% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Prance (2009) | 25 | 0.03% | 7 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Rodríguez-Mirón (2018) | 25 | 0.03% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Soldati & Touroult (2014) | 25 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Taylor & Glover (2016) | 25 | 0.03% | 25 | 0.07% | 25 | 0.08% | 25 | 0.08% |
Batista et al. (2008) | 24 | 0.03% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Bily & Brûlé (2013) | 24 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Carré (2006) | 24 | 0.03% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Chalumeau & Touroult (2005) | 24 | 0.03% | 22 | 0.06% | 17 | 0.05% | 22 | 0.07% |
Chen et al. (2018) | 24 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Cochereau (1966) | 24 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Evangelista et al. (2019) | 24 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Heller (1916) | 24 | 0.03% | 15 | 0.04% | 15 | 0.05% | 14 | 0.04% |
Kylin et al. (2012) | 24 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Linné (1766) | 24 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mcallister et al. (2010) | 24 | 0.03% | 6 | 0.02% | 5 | 0.02% | 6 | 0.02% |
Melo (2007) | 24 | 0.03% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Mestier et al. (2022) | 24 | 0.03% | 18 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Morales (2006) | 24 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Morvan & Roguet (2014) | 24 | 0.03% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Raynal (1976) | 24 | 0.03% | 4 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Rheinheimer (2023) | 24 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Schaus (1906) | 24 | 0.03% | 15 | 0.04% | 15 | 0.05% | 13 | 0.04% |
Sidlauskas & Vari (2012) | 24 | 0.03% | 24 | 0.07% | 24 | 0.07% | 24 | 0.07% |
Talaga et al. (2021) | 24 | 0.03% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Tavakilian & Peñaherrera-leiva (2005) | 24 | 0.03% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Weimerskirch et al. (2009) | 24 | 0.03% | 18 | 0.05% | 18 | 0.06% | 10 | 0.03% |
Abraham (2021) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 22 | 0.07% |
Adamonyte et al. (2011) | 23 | 0.03% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Ballerio (2014) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Barbut (2022) | 23 | 0.03% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Bousquet (2018) | 23 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer (2023) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Brévignon (2005) | 23 | 0.03% | 19 | 0.06% | 9 | 0.03% | 16 | 0.05% |
Delfosse et al. (2019) | 23 | 0.03% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
dos Santos et al. (2021) | 23 | 0.03% | 23 | 0.07% | 22 | 0.07% | 23 | 0.07% |
Gomes et al. (2022) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Gonzales et al. (2015) | 23 | 0.03% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Gutierrez (1981) | 23 | 0.03% | 21 | 0.06% | 21 | 0.06% | 20 | 0.06% |
Howard (1973) | 23 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 23 | 0.03% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Maas et al. (2003) | 23 | 0.03% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Moonen (2013) | 23 | 0.03% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Ormerod (2009) | 23 | 0.03% | 1 | 0% | 1 | 0% | 1 | 0% |
Pierre & Lalanne-Cassou | 23 | 0.03% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Rodrigues et al. (2022) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Sambin (2018) | 23 | 0.03% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Schmidt & Shattuck (2014) | 23 | 0.03% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Tavakilian & Néouze (2007) | 23 | 0.03% | 23 | 0.07% | 23 | 0.07% | 23 | 0.07% |
Bauters et al. (2014) | 22 | 0.03% | 1 | 0% | 1 | 0% | 1 | 0% |
Berry et al. (2004) | 22 | 0.03% | 5 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Boilly et al. (2016) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 21 | 0.06% |
Bright (2019) | 22 | 0.03% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Antenor, 3(1): 65-77.">Cerda (2016) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Christenhusz (2002) | 22 | 0.03% | 18 | 0.05% | 15 | 0.05% | 16 | 0.05% |
Curletti & Brûlé (2014) | 22 | 0.03% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Desbrochers des Loges (1890) | 22 | 0.03% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Fairmaire (1847) | 22 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Fallon (2016) | 22 | 0.03% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Grose & Olmstead (2007) | 22 | 0.03% | 13 | 0.04% | 11 | 0.03% | 12 | 0.04% |
Iles et al. (2017) | 22 | 0.03% | 22 | 0.06% | 21 | 0.06% | 19 | 0.06% |
Ingels et al. (2003) | 22 | 0.03% | 20 | 0.06% | 20 | 0.06% | 17 | 0.05% |
Itrac-bruneau & Doucet (2022) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Itrac-Bruneau & Doucet (2023) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Jay et al. (2009) | 22 | 0.03% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Kuijt (2011) | 22 | 0.03% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Lombardi (2016) | 22 | 0.03% | 8 | 0.02% | 7 | 0.02% | 8 | 0.02% |
McVaugh (1969) | 22 | 0.03% | 8 | 0.02% | 6 | 0.02% | 8 | 0.02% |
Meyrick (1934-1936) | 22 | 0.03% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Mickel (2016) | 22 | 0.03% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Mori et al. (2002) | 22 | 0.03% | 20 | 0.06% | 20 | 0.06% | 19 | 0.06% |
Roguet (2022) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Santschi (1929) | 22 | 0.03% | 1 | 0% | 1 | 0% | 1 | 0% |
Taczanowski (1874) | 22 | 0.03% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Waller et al. (1990) | 22 | 0.03% | 22 | 0.06% | 22 | 0.07% | 22 | 0.07% |
Alston et al. (1981) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Barbosa & Azevedo (2018) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Barneby (1991) | 21 | 0.02% | 7 | 0.02% | 2 | 0.01% | 3 | 0.01% |
Mosquito Systematics, 8(2): 163-193.">Belkin & Heinemann (1976) | 21 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Braet (2014) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Chanderbali (2004) | 21 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Chew (1969) | 21 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Dyar (1910) | 21 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Fabricius (1805) | 21 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Faivovich et al. (2005) | 21 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Feuillet (2013) | 21 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Fraga (2012) | 21 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Guimarães et al. (2017) | 21 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Harley & Pastore (2012) | 21 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Lewis (2000) | 21 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Lupoli (2019) | 21 | 0.02% | 20 | 0.06% | 20 | 0.06% | 19 | 0.06% |
Mertens & Wermuth (1960) | 21 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nesheim et al. (2017) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Pavlíček & Csuzdi (2012) | 21 | 0.02% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Plowman et al. (1998) | 21 | 0.02% | 6 | 0.02% | 5 | 0.02% | 5 | 0.02% |
Prévoteau (2012) | 21 | 0.02% | 21 | 0.06% | 18 | 0.06% | 18 | 0.05% |
Rudd (1955) | 21 | 0.02% | 11 | 0.03% | 6 | 0.02% | 6 | 0.02% |
Sagot (1882) | 21 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Senevet & Abonnenc (1939) | 21 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Smidt (2007) | 21 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Spina et al. (2013) | 21 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Talaga et al. (2015) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Taylor (2015) | 21 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Touroult et al. (2018) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Trethowan et al. (2015) | 21 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Van Soest (2017) | 21 | 0.02% | 21 | 0.06% | 21 | 0.06% | 21 | 0.06% |
Wheeler (1935) | 21 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Andrino et al. (2023) | 20 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Beaucournu et al. (1998) | 20 | 0.02% | 20 | 0.06% | 12 | 0.04% | 14 | 0.04% |
Becker (2021) | 20 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Bordin et al. (2021) | 20 | 0.02% | 20 | 0.06% | 20 | 0.06% | 12 | 0.04% |
Brévignon & Gallard (1998) | 20 | 0.02% | 17 | 0.05% | 5 | 0.02% | 15 | 0.05% |
Cárdenas et al. (2019) | 20 | 0.02% | 18 | 0.05% | 10 | 0.03% | 14 | 0.04% |
Cetzal-Ix et al. (2016) | 20 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Chassain & Touroult (2016) | 20 | 0.02% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Cornejo (2020) | 20 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Dognin (1908) | 20 | 0.02% | 8 | 0.02% | 8 | 0.02% | 6 | 0.02% |
Etienne & Vilardebó (1978) | 20 | 0.02% | 18 | 0.05% | 18 | 0.06% | 16 | 0.05% |
. Publications de l’Institut Pasteur de la Guyane, 20: 1-22.">Floch & Abonnenc (1941) | 20 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Fourriére et al. (2014) | 20 | 0.02% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Gates (1982) | 20 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Gregório et al. (2023) | 20 | 0.02% | 17 | 0.05% | 17 | 0.05% | 16 | 0.05% |
Griffiths & Florens (2006) | 20 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Guéguen (2000) | 20 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Horn (1994) | 20 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Jansen-jacobs & Meijer (1995) | 20 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Leavengood et al. (2024) | 20 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Lethierry (1881) | 20 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Manzitto‐Tripp & Daniel (2023) | 20 | 0.02% | 20 | 0.06% | 20 | 0.06% | 18 | 0.05% |
Motta et al. (2018) | 20 | 0.02% | 20 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Peck (2016) | 20 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Prado & Moran (2008) | 20 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Rageau (1958) | 20 | 0.02% | 18 | 0.05% | 18 | 0.06% | 16 | 0.05% |
Salino et al. (2015) | 20 | 0.02% | 11 | 0.03% | 8 | 0.02% | 8 | 0.02% |
Schaus (1892) | 20 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Suddee et al. (2004) | 20 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Webster (1956) | 20 | 0.02% | 6 | 0.02% | 2 | 0.01% | 5 | 0.02% |
Ythier et al. (2020) | 20 | 0.02% | 20 | 0.06% | 20 | 0.06% | 20 | 0.06% |
Amshoff (1939) | 19 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Bayón (2015) | 19 | 0.02% | 3 | 0.01% | 2 | 0.01% | 1 | 0% |
Bénéluz & Gallard (2012) | 19 | 0.02% | 19 | 0.06% | 6 | 0.02% | 19 | 0.06% |
Biral (2016) | 19 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonfils (1969) | 19 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Borkent & Wirth (1997) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Cassola (2011) | 19 | 0.02% | 16 | 0.05% | 13 | 0.04% | 14 | 0.04% |
Charrassin (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Charrassin (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Chassain & Touroult (2018) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Dumbardon-Martial & Delblond (2019) | 19 | 0.02% | 16 | 0.05% | 16 | 0.05% | 11 | 0.03% |
Eigenmann (1912) | 19 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Fabricius (1798) | 19 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Faynel et al. (2003) | 19 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gardner et al. (2021) | 19 | 0.02% | 15 | 0.04% | 15 | 0.05% | 9 | 0.03% |
Girón & Short (2021) | 19 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Haynes & Holm-nielsen (2009) | 19 | 0.02% | 9 | 0.03% | 7 | 0.02% | 7 | 0.02% |
Irmler (2014) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Irwin & Barneby (1982) | 19 | 0.02% | 9 | 0.03% | 4 | 0.01% | 5 | 0.02% |
Jarrett & Shirihai (2014) | 19 | 0.02% | 18 | 0.05% | 18 | 0.06% | 10 | 0.03% |
Luc & Coomans (1992) | 19 | 0.02% | 19 | 0.06% | 17 | 0.05% | 19 | 0.06% |
Luer (1989) | 19 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Moutou (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Olivier (1789) | 19 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Packauskas (2010) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Ponchel (2015) | 19 | 0.02% | 18 | 0.05% | 18 | 0.06% | 17 | 0.05% |
Rasmussen et al. (2007) | 19 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Rheinheimer (2015) | 19 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Rheinheimer (2018) | 19 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Sabroux et al. (2022) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 19 | 0.06% |
Sanborn (2016) | 19 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Soto Arenas & Cribb (2010) | 19 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Spitz et al. (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Taylor & Hollowell (2016) | 19 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Thoisy & Bordin (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Uicn et al. (2015) | 19 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Urtizberea (2016) | 19 | 0.02% | 19 | 0.06% | 19 | 0.06% | 11 | 0.03% |
Austin (1998) | 18 | 0.02% | 5 | 0.01% | 2 | 0.01% | 4 | 0.01% |
Batista et al. (2011) | 18 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Berland (1933) | 18 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Bouchon-Navaro et al. (1992) | 18 | 0.02% | 15 | 0.04% | 15 | 0.05% | 14 | 0.04% |
Braet et al. (2003) | 18 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Brévignon (2021) | 18 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Carvalho et al. (2000) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Clavier (2023) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Clements et al. (2015) | 18 | 0.02% | 18 | 0.05% | 10 | 0.03% | 13 | 0.04% |
Colletta et al. (2020) | 18 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Cuatrecasas (1964) | 18 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Dierkens (2014) | 18 | 0.02% | 18 | 0.05% | 15 | 0.05% | 17 | 0.05% |
Ebihara et al. (2006) | 18 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Erwin (2011) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Fabricius (1792) | 18 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 18 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Felder & Rogenhofer (1864-1867) | 18 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldmann (2014) | 18 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Freytag (2006) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Gaimari & Silva (2020) | 18 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Epidendrum". Icones Orchidacearum, 11: pls. 1101-1200.">Hágsater (2008) | 18 | 0.02% | 7 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Karremans et al. (2016) | 18 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Landrum (1986) | 18 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Löfstrand et al. (2021) | 18 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Lourenço (1983) | 18 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Mazine et al. (2018) | 18 | 0.02% | 16 | 0.05% | 16 | 0.05% | 15 | 0.05% |
Meneguzzo & van den Berg (2020) | 18 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Monné & Tavakilian (2011) | 18 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Morillo (2015) | 18 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Nielson (1979) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Oláh & Johanson (2012) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Opitz (2019) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Patel & Singh (2016) | 18 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Paulian (1998) | 18 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Pilsbry (1906-1907) | 18 | 0.02% | 4 | 0.01% | 4 | 0.01% | 2 | 0.01% |
Plowman & Hensold (2004) | 18 | 0.02% | 18 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Quate & Brown (2004) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Ramage (2014) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Ratcliffe (2018) | 18 | 0.02% | 18 | 0.05% | 16 | 0.05% | 18 | 0.05% |
Roguet (2022) | 18 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Sambin & Chiron (2015) | 18 | 0.02% | 7 | 0.02% | 4 | 0.01% | 6 | 0.02% |
Simões & Staples (2017) | 18 | 0.02% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Staines & García-robledo (2014) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Steyermark (1965) | 18 | 0.02% | 4 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Taylor (1994) | 18 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Tippery et al. (2024) | 18 | 0.02% | 18 | 0.05% | 18 | 0.06% | 18 | 0.05% |
Vaurie (1976) | 18 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Wiersema et al. (2008) | 18 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Wunderlin (2010) | 18 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Yang et al. (2012) | 18 | 0.02% | 17 | 0.05% | 17 | 0.05% | 15 | 0.05% |
Andersson & Kennedy (1986) | 17 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barfuss et al. (2016) | 17 | 0.02% | 8 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Biral et al. (2017) | 17 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Blanco et al. (2008) | 17 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Braet & Quicke (2004) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Brévignon (2011) | 17 | 0.02% | 15 | 0.04% | 9 | 0.03% | 15 | 0.05% |
Chalumeau (1983) | 17 | 0.02% | 16 | 0.05% | 16 | 0.05% | 15 | 0.05% |
Corbari et al. (2020) | 17 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Courtial et al. (2014) | 17 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Delrieu-Trottin et al. (2015) | 17 | 0.02% | 17 | 0.05% | 16 | 0.05% | 17 | 0.05% |
Denham (2005) | 17 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Dewynter et al. (2019) | 17 | 0.02% | 16 | 0.05% | 16 | 0.05% | 13 | 0.04% |
Dos Santos Junior et al. (2015) | 17 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Drew et al. (2017) | 17 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Dupont et al. (2023) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Emery (1911) | 17 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Černosvitov (1934) | 17 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Fernandes & Grazia (2006) | 17 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Fisher & Fong (2020) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Galea (2013) | 17 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Goldblatt & Snow (1991) | 17 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Gordon et al. (2013) | 17 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Grolle (1995) | 17 | 0.02% | 9 | 0.03% | 9 | 0.03% | 8 | 0.02% |
Hammes & Putoa (1986) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Hassemer (2017) | 17 | 0.02% | 5 | 0.01% | 3 | 0.01% | 4 | 0.01% |
Hennemann et al. (2018) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Hustache (1951) | 17 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Kazandjian (2017) | 17 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Lachenaud et al. (2022) | 17 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Lehnert (2012) | 17 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Martins (1976) | 17 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Meyrick (1917) | 17 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Miers (1878) | 17 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Moraes et al. (2010) | 17 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Nesom (2009) | 17 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Orrell (2019) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Pellegrini et al. (2018) | 17 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Pessoa & Alves (2016) | 17 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Prance & Sothers (2003) | 17 | 0.02% | 17 | 0.05% | 14 | 0.04% | 15 | 0.05% |
Rainer (2007) | 17 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Roalson et al. (2010) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 16 | 0.05% |
Salisbury (1796) | 17 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Seigler et al. (2006) | 17 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Silva (1976) | 17 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Souza et al. (2021) | 17 | 0.02% | 16 | 0.05% | 14 | 0.04% | 12 | 0.04% |
Spina (2004) | 17 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Tarmann & Drouet (2015) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Tavakilian & Santos-Silva (2019) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 17 | 0.05% |
Taylor (1992) | 17 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Taylor (2001) | 17 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Toutain (1989) | 17 | 0.02% | 13 | 0.04% | 13 | 0.04% | 12 | 0.04% |
Tröndlé & Boutet (2009) | 17 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Wiersema et al. (2018) | 17 | 0.02% | 6 | 0.02% | 5 | 0.02% | 5 | 0.02% |
Zuloaga et al. (2018) | 17 | 0.02% | 17 | 0.05% | 17 | 0.05% | 15 | 0.05% |
Arnaud (2002) | 16 | 0.02% | 14 | 0.04% | 14 | 0.04% | 13 | 0.04% |
Bacchet et al. (2007) | 16 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Baglan & Catzeflis (2016) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Bar (1875) | 16 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Barau et al. (2005) | 16 | 0.02% | 13 | 0.04% | 13 | 0.04% | 10 | 0.03% |
Bérenger (2001) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Bernardi (2000) | 16 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Boisduval (1875) | 16 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulard & Martinelli (1996) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Braet (2002) | 16 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Brechlin et al. (2016) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Brindle (1971) | 16 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Carmona-Suárez & Poupin (2016) | 16 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Casey (1922) | 16 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Chassain (2010) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Cohic (1959) | 16 | 0.02% | 13 | 0.04% | 13 | 0.04% | 12 | 0.04% |
Cupello (2018) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Degallier & Tishechkin (2022) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Dewynter et al. (2023) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Dierkens (2011) | 16 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Dognin (1909) | 16 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Drouët (1859) | 16 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Dupuis (2016) | 16 | 0.02% | 10 | 0.03% | 9 | 0.03% | 10 | 0.03% |
Feuillet (2016) | 16 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Fournier et al. (2019) | 16 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Fourt et al. (2017) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Garrigue (2007) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 10 | 0.03% |
G.E.M.M. (2012) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 9 | 0.03% |
Herbulot (1993) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Justine et al. (2021) | 16 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Kobuski (1942) | 16 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Krüger et al. (2018) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Kuijt (2014) | 16 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Kury et al. (2024) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Lanjouw (1935) | 16 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Lehnert (2011) | 16 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Lopes et al. (2021) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 13 | 0.04% |
Luer (2010) | 16 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Marek (2015) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Massary et al. (2021) | 16 | 0.02% | 16 | 0.05% | 15 | 0.05% | 13 | 0.04% |
Mermudes (2005) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Monné et al. (2020) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Perrault (1988) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Pirani (1990) | 16 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Puthz (2012) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Renz (1992) | 16 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Santos-Silva et al. (2018) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 16 | 0.05% |
Schneider & Zizka (2012) | 16 | 0.02% | 7 | 0.02% | 3 | 0.01% | 5 | 0.02% |
Schneider & Zizka (2017) | 16 | 0.02% | 15 | 0.04% | 14 | 0.04% | 13 | 0.04% |
Sekerka (2014) | 16 | 0.02% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Söderström et al. (2013) | 16 | 0.02% | 6 | 0.02% | 4 | 0.01% | 5 | 0.02% |
Swanson (2018) | 16 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Taylor (1997) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 14 | 0.04% |
Touroult et al. (2019) | 16 | 0.02% | 16 | 0.05% | 16 | 0.05% | 15 | 0.05% |
Vasselon et al. (2019) | 16 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Walker (1854) | 16 | 0.02% | 2 | 0.01% | 2 | 0.01% | 1 | 0% |
Arriagada (2003) | 15 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Aulagnier (2009) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 10 | 0.03% |
Bellanger et al. (2018) | 15 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Blackwelder (1943) | 15 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Borkent (2008) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Brown & Kung (2007) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Cerda (2014) | 15 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Dalens et al. (2010) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Delvare (1992) | 15 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Deuve (2005) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Dierkens (2012) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Fabricius ([1777]) | 15 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 15 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Fournier & Lechat (2016) | 15 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Fryxell (2001) | 15 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Gannier (2001) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 9 | 0.03% |
Génier (2009) | 15 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Herbin (2022) | 15 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Hinton (1940) | 15 | 0.02% | 15 | 0.04% | 14 | 0.04% | 13 | 0.04% |
Ifremer (2009) | 15 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Imshaug (2019) | 15 | 0.02% | 13 | 0.04% | 13 | 0.04% | 12 | 0.04% |
Jennings et al. (2013) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Joicey & Talbot ([1918]) | 15 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Jordan (1924) | 15 | 0.02% | 9 | 0.03% | 6 | 0.02% | 8 | 0.02% |
Kubitzki (1971) | 15 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Lapèze (2021) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Lorvelec et al. (2007) | 15 | 0.02% | 14 | 0.04% | 14 | 0.04% | 12 | 0.04% |
Maddi (2014) | 15 | 0.02% | 9 | 0.03% | 9 | 0.03% | 8 | 0.02% |
Mantilleri & Sforzi (2006) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Miller (1768) | 15 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Morvan & Morati (2011) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Mynssen (2011) | 15 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Nelson-Smith et al. (2014) | 15 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Øllgaard & Windisch (2016) | 15 | 0.02% | 3 | 0.01% | 3 | 0.01% | 2 | 0.01% |
Peraza-Flores et al. (2011) | 15 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Philcox (1970) | 15 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Plumel (1991) | 15 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Puthz (2015) | 15 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Redden et al. (2018) | 15 | 0.02% | 10 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Reeb et al. (2022) | 15 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Rheinheimer (2020) | 15 | 0.02% | 15 | 0.04% | 15 | 0.05% | 15 | 0.05% |
Sakakibara (2013) | 15 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Sanín et al. (2023) | 15 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Santos-Silva et al. (2021) | 15 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Sastre & Offroy (2016) | 15 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Shelley et al. (1984) | 15 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Simpson (1992) | 15 | 0.02% | 9 | 0.03% | 6 | 0.02% | 6 | 0.02% |
Soderstrom & Zuloaga (1989) | 15 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Szpigel (2024) | 15 | 0.02% | 13 | 0.04% | 13 | 0.04% | 11 | 0.03% |
Toledo et al. (2020) | 15 | 0.02% | 8 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Villiers (1971) | 15 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Vivallo (2019) | 15 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Voss et al. (2001) | 15 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Aguirre-Santoro (2017) | 14 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Ament & Amorim (2013) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Ardila-Camacho et al. (2024) | 14 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Armbruster et al. (2009) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 13 | 0.04% |
Bonne-wepster & Bonne (1920) | 14 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Braz & Monteiro (2017) | 14 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Brévignon (2019) | 14 | 0.02% | 12 | 0.03% | 9 | 0.03% | 11 | 0.03% |
Calvert (1909) | 14 | 0.02% | 11 | 0.03% | 10 | 0.03% | 11 | 0.03% |
Candolle (1869) | 14 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carvalho-silva et al. (2017) | 14 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Cerda (2017) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Constantin (2013) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Coomans (1967) | 14 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Delgado-Salinas et al. (2011) | 14 | 0.02% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Delprete et al. (2021) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Dewynter et al. (2019) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 12 | 0.04% |
Dewynter et al. (2021) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 10 | 0.03% |
Emery (1890) | 14 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Enroth et al. (2019) | 14 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Ferrer (2011) | 14 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2019) | 14 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Garrouste & Hervé (2009) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Gentry (1973) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
González‐Elizondo & Peterson (1997) | 14 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Hash & Brown (2015) | 14 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Horeau et al. (2005) | 14 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Irmler (2015) | 14 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Irmler (2017) | 14 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Jordan (1904) | 14 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Jost et al. (2019) | 14 | 0.02% | 12 | 0.03% | 11 | 0.03% | 12 | 0.04% |
Kitching et al. (2018) | 14 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Kubitzki & Renner (1982) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Lachenaud et al. (2021) | 14 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Lamas (2004) | 14 | 0.02% | 4 | 0.01% | 2 | 0.01% | 3 | 0.01% |
Lourenço et al. (2018) | 14 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Marceniuk & Menezes (2007) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Mathias & Theobald (1981) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Mickel (1938) | 14 | 0.02% | 14 | 0.04% | 12 | 0.04% | 13 | 0.04% |
Morrison (1997) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Munroe (1970) | 14 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Murphy (1986) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Desmodium incanum and Fall of D. canum (Fabaceae). Taxon, 27(4): 365-370.">Nicolson (1978) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Ormerod (2018) | 14 | 0.02% | 4 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Peñaherrera-Leiva & Tavakilian (2003) | 14 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Prout (1932-1938) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Razafimandimbison & Bremer (2011) | 14 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Rheinheimer (2012) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Rheinheimer (2017) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Rivoire (2018) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 12 | 0.04% |
Scatigna et al. (2022) | 14 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Senevet (1937) | 14 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Smith & Cognato (2021) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Stoll ([1787-1790]) | 14 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor (1987) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Thiaucourt (1997) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Tostain (1980) | 14 | 0.02% | 10 | 0.03% | 10 | 0.03% | 8 | 0.02% |
Toulgoët (1987) | 14 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Ulysséa & Brandão (2021) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
van Ee et al. (2011) | 14 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Vanin (1986) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Withner (1993) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Yvinec (2013) | 14 | 0.02% | 14 | 0.04% | 14 | 0.04% | 14 | 0.04% |
Zardini & Raven (1991) | 14 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Zuntini et al. (2015) | 14 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Barbut & Lalanne-Cassou (2010) | 13 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Barbut & Lalanne-cassou (2016) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Berland (1934) | 13 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Blanco (2013) | 13 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Borges & Couri (2009) | 13 | 0.02% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Bouget et al. (2019) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Bouman et al. (2022) | 13 | 0.02% | 9 | 0.03% | 9 | 0.03% | 7 | 0.02% |
Brandbyge (1986) | 13 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Butler (1878) | 13 | 0.02% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Chassain & Touroult (2013) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Chautems & Perret (2013) | 13 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Cheesman (1928) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Clavier et al. (2018) | 13 | 0.02% | 12 | 0.03% | 11 | 0.03% | 12 | 0.04% |
Compagno (1984) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Courtial et al. (2022) | 13 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Deblock et al. (1960) | 13 | 0.02% | 7 | 0.02% | 7 | 0.02% | 6 | 0.02% |
Delprete & Persson (2012) | 13 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Denux & Zagatti (2010) | 13 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Deshayes (1863) | 13 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupuis (2017) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 11 | 0.03% |
D'arcy (1987) | 13 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Erichson (1839-1840) | 13 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2015) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Evrard et al. (2004) | 13 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Fontella Pereira (1977) | 13 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Gannier (2002) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 9 | 0.03% |
Gannier (2009) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 9 | 0.03% |
Georgiev (2023) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Graham (1988) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Guenée (1852) | 13 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Guillermet (2011) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Hassemer et al. (2017) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 11 | 0.03% |
Heemstra & Randall (1993) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Héros et al. (2007) | 13 | 0.02% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Juhel & Dalens (2017) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Laguerre (2017) | 13 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Lattke (1995) | 13 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lees et al. (2014) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Lesne (1932) | 13 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Lim et al. (2002) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Meneguzzo et al. (2015) | 13 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Miller (2009) | 13 | 0.02% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Monne & Fragoso (1988) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Monné et al. (2020) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Oliveira Pellegrini & Forzza (2017) | 13 | 0.02% | 1 | 0% | 1 | 0% | 0 | 0% |
Orellana & Barrios (2021) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Osborn (1938) | 13 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Rheinheimer (2010) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Rheinheimer (2014) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Rheinheimer (2019) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Riina et al. (2021) | 13 | 0.02% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Roux & Coll (2020) | 13 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Difforme". Richardiana, nouvelle série, 2: 40-71.">Sambin et al. (2018) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Schwartsburd & Prado (2016) | 13 | 0.02% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Seigler & Ebinger (2015) | 13 | 0.02% | 1 | 0% | 1 | 0% | 1 | 0% |
Sharkey (1988) | 13 | 0.02% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Soula (2002) | 13 | 0.02% | 9 | 0.03% | 9 | 0.03% | 8 | 0.02% |
Terra-Araujo et al. (2016) | 13 | 0.02% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
The International Barcode of Life Consortium (2016) | 13 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Theobald (1903) | 13 | 0.02% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Tieghem & Van (1895) | 13 | 0.02% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Toulgoet (1992) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Wagner et al. (2007) | 13 | 0.02% | 13 | 0.04% | 13 | 0.04% | 13 | 0.04% |
Walenkamp (1979) | 13 | 0.02% | 11 | 0.03% | 11 | 0.03% | 10 | 0.03% |
Wallnöfer (2000) | 13 | 0.02% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Wilson & Taylor (1967) | 13 | 0.02% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Bates (1870) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Bérenger (2007) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Berry & Smith-Vaniz (1978) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Berry et al. (2001) | 12 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Boilly (2018) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Boulard (1986) | 12 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Bright (2014) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Broomfield (1976) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Bruggeman-Nannenga & Arts (2010) | 12 | 0.01% | 7 | 0.02% | 7 | 0.02% | 6 | 0.02% |
Byles et al. (2013) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Camino et al. (2008) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Catzeflis (2014) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 9 | 0.03% |
Cazanove (2022) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Antenor, 4(2): 158-163, 14 fig.">Cerda (2017) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Chainey (2005) | 12 | 0.01% | 8 | 0.02% | 8 | 0.02% | 5 | 0.02% |
Chani-Posse et al. (2018) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Chassain & Touroult (2017) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Chopard (1912) | 12 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Cochereau (1974) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 10 | 0.03% |
Compagno (1984) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Copeland (1932) | 12 | 0.01% | 8 | 0.02% | 8 | 0.02% | 4 | 0.01% |
Cordeiro & Moreira (2015) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Cornejo & Iltis (2007) | 12 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Covain et al. (2012) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Cremers & Hoff (1995) | 12 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Curletti & Brûlé (2023) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Curletti & Brûlé (2023) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Dalens & Touroult (2014) | 12 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Daly (1992) | 12 | 0.01% | 12 | 0.03% | 4 | 0.01% | 12 | 0.04% |
Daniel & Mcdade (2014) | 12 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Daugeron et al. (2024) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Decraemer (1983) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Degallier (2004) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Deuve (2018) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Dewynter et al. (2017) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2023) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 10 | 0.03% |
Diaw (1976) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Dognin (1906) | 12 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Erwin (1982) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Fabricius (1781) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiedler (1935) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Freytag (2013) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Gannier (2000) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 8 | 0.02% |
Gibeaux (2020) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Gradstein & Costa (2003) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson (1998) | 12 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Hayden (1990) | 12 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Heiss & Moragues (2015) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Herbin (2017) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Herrich-schaeffer (1850-[1869]) | 12 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Hielkema (2017) | 12 | 0.01% | 5 | 0.01% | 5 | 0.02% | 4 | 0.01% |
Humala (2017) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Hustache (1937) | 12 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Irmler (2003) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Jabiol et al. (2013) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Kurina & Hippa (2021) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Kuschel (1983) | 12 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Laguerre (2016) | 12 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Laurent et al. (2020) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Lemaire (2002) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Logunov (2015) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Lombardi (2000) | 12 | 0.01% | 5 | 0.01% | 4 | 0.01% | 5 | 0.02% |
Mantilleri (2012) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Marinho et al. (2019) | 12 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Massary et al. (2018) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 10 | 0.03% |
Mazur (1984) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Mendonca et al. (2021) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Miller (2009) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Monné & Tavakilian (2002) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Morawetz (2007) | 12 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Nearns & Tavakilian (2015) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Oort (1939) | 12 | 0.01% | 3 | 0.01% | 2 | 0.01% | 3 | 0.01% |
Ortiz-Sepulveda et al. (2019) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Paula-Souza & Pirani (2014) | 12 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Rocamora (2004) | 12 | 0.01% | 11 | 0.03% | 10 | 0.03% | 9 | 0.03% |
Roguet (2022) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Runyon & Pollet (2018) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Schaus (1924) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnell (1969) | 12 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Sculfort & Dewynter (2024) | 12 | 0.01% | 12 | 0.03% | 8 | 0.02% | 11 | 0.03% |
Silva (1986) | 12 | 0.01% | 7 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Silvestri (1897) | 12 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Sites et al. (2024) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Smith et al. (2006) | 12 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Soares et al. (2013) | 12 | 0.01% | 5 | 0.01% | 5 | 0.02% | 4 | 0.01% |
Solomon et al. (2019) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Stevenson & Zanoni (1991) | 12 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Tavakilian & Santos-silva (2022) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Thiaucourt (2001) | 12 | 0.01% | 12 | 0.03% | 12 | 0.04% | 12 | 0.04% |
Uicn et al. (2019) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Ulloa et al. (2019) | 12 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Van Dijk et al. (2014) | 12 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (1991) | 12 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Waichert et al. (2015) | 12 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Wheeler (1932) | 12 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Wibmer & O'brien (1986) | 12 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Zerega et al. (2005) | 12 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Allen (1985) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Almeida et al. (2016) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 10 | 0.03% |
Anonyme (1874) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbut & Lalanne-Cassou (2019) | 11 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Batista et al. (2018) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Bauer (2003) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Baum et al. (1983) | 11 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Bérenger & Gil-Santana (2005) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Bernard et al. (2014) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Beron (2021) | 11 | 0.01% | 11 | 0.03% | 10 | 0.03% | 11 | 0.03% |
Binetruy et al. (2019) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Boucek & Delvare (1992) | 11 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Boulard (1971) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Bouman et al. (2020) | 11 | 0.01% | 4 | 0.01% | 4 | 0.01% | 1 | 0% |
Braet & van Achterberg (2001) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Braun et al. (2014) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Breuning (1940) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Brito et al. (2024) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 7 | 0.02% |
Brosse et al. (2021) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Candolle (1849) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Cardiel et al. (2022) | 11 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Cremers & Hoff (2000) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Cuvier & Valenciennes ([1832]) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2022) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 9 | 0.03% |
Dubois (2017) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Dupont et al. (2023) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Dwyer (1958) | 11 | 0.01% | 5 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Eger (1978) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Fauvel (1867) | 11 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Feuillet (2016) | 11 | 0.01% | 4 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Fiaschi et al. (2020) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Fukushima & Bertani (2017) | 11 | 0.01% | 2 | 0.01% | 2 | 0.01% | 0 | 0% |
Génier & Arnaud (2016) | 11 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gibon & Sganga (2019) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Gomes (2006) | 11 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Graham et al. (2021) | 11 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Graham (2017) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Grazziotin et al. (2012) | 11 | 0.01% | 9 | 0.03% | 9 | 0.03% | 7 | 0.02% |
Gruhn & Rödel (2020) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Guillermet (2004) | 11 | 0.01% | 7 | 0.02% | 7 | 0.02% | 4 | 0.01% |
Hamada & Fouque (2001) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Hansen (1980) | 11 | 0.01% | 1 | 0% | 0 | 0% | 1 | 0% |
Hemming (1937) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Hippa & Kurina (2013) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Hoff & Cremers (2005) | 11 | 0.01% | 9 | 0.03% | 6 | 0.02% | 9 | 0.03% |
Hoffman et al. (2002) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Hunt (1986) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Justine (2018) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Kiszka et al.(2007) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 7 | 0.02% |
Koch (1844) | 11 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Komarek (2005) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Konno & Fontella Pereira (2004) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Kyalangalilwa et al. (2013) | 11 | 0.01% | 4 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Lachenaud et al. (2022) | 11 | 0.01% | 8 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Lapèze et al. (2022) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Laran et al. (2011) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 8 | 0.02% |
Laurent et al. (2018) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Lebas et al. (2016) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Lyons & Snyder (2019) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Maas et al. (1986) | 11 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Marhold et al. (2016) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Marquet & Roguet (2003) | 11 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Monti et al. (2010) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Moran et al. (2010) | 11 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Mori & Prance (1990) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Morrison (1996) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Möschler (1872) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 7 | 0.02% |
Opitz (2018) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Ormerod (2016) | 11 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Padua et al. (2020) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Pascoe (1881) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Patchell et al. (2014) | 11 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Poncy (1991) | 11 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Prance (2009) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Prié (2020) | 11 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Prout (1916) | 11 | 0.01% | 7 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Questel et al. (2023) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 9 | 0.03% |
Questel et al. (2023) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 9 | 0.03% |
Questel (2022) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Renner & Hausner (2005) | 11 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Rheinheimer (2014) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Ribeiro (2005) | 11 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Richards (1978) | 11 | 0.01% | 4 | 0.01% | 0 | 0% | 4 | 0.01% |
Rojas-alvarado (2017) | 11 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Pseudepidendrum". Richardiana, nouvelle série, 2: 97-135.">Sambin et al. (2018) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Sanders (2012) | 11 | 0.01% | 6 | 0.02% | 4 | 0.01% | 4 | 0.01% |
Selys Longchamps (1853) | 11 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Silva et al. (2019) | 11 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
St Laurent & Dombroskie (2016) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Stoll (1782) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Szlachetko (2012) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Thomson (1859) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Todd (1920) | 11 | 0.01% | 6 | 0.02% | 2 | 0.01% | 6 | 0.02% |
Touroult et al. (2010) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 11 | 0.03% |
Touroult et al. (2020) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Val (1976) | 11 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Walker ([1865]) | 11 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Wasshausen (2006) | 11 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Wenzel (1976) | 11 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Wiedemann (1828) | 11 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Zuo et al. (2024) | 11 | 0.01% | 11 | 0.03% | 11 | 0.03% | 9 | 0.03% |
Allorge & Poupat (1991) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Allorge (1985) | 10 | 0.01% | 2 | 0.01% | 1 | 0% | 1 | 0% |
Andouche et al. (2020) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Audureau & Morvan (2019) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Azevedo Tozzi & Silva (2007) | 10 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Barber (1930) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Becker & Miller (1988) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Béreau (2017) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Blard et al. (2003) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Blatrix et al. (2018) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Boilly (2011) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Borges et al. (2022) | 10 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Borowiec (1996) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Boulard & Martinelli (2011) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Braet et al. (2014) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Brechlin & Meister (2011) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Brévignon & Lamas (1993) | 10 | 0.01% | 6 | 0.02% | 0 | 0% | 6 | 0.02% |
Brevignon (2013) | 10 | 0.01% | 10 | 0.03% | 8 | 0.02% | 10 | 0.03% |
Brévignon (2013) | 10 | 0.01% | 8 | 0.02% | 4 | 0.01% | 8 | 0.02% |
Brito et al. (2017) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Calió et al. (2017) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Carrijo et al. (2023) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Caterino & Tishechkin (2014) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Chassain & Touroult (2012) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Cherot & Carpintero (2017) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Christenhusz (2010) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Clastrier & Wirth (1995) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Clausen (1938) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Couté & Garrouste (2009) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Curletti & Brûlé (2021) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
de Toulgoët (2001) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Del Hoyo & Collar (2014) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Delprete et al. (2010) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Delprete (2020) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Desutter-Grandcolas (1992) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Deuve (2004) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Dewynter et al. (2020) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Dognin (1911) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Ducke (1904) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Dyar (1910) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Dyar (1914) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Fauvel (1903) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Fauvel (1904) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Félix et al. (2014) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Ferrer & Moragues (1998) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Filardi et al. (2013) | 10 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Fleutiaux & Sallé ([1890]) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
França & Giulietti (2012) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Freytag & Delong (1982) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Freytag (2008) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Galea (2010) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Garriques & Lamy (2017) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gere (2013) | 10 | 0.01% | 8 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Géry et al. (1991) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Goding (1929) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Gonzales & Yvinec (2016) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Gradstein & Lavocat Bernard (2020) | 10 | 0.01% | 4 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Gradstein (2015) | 10 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Grolle (2002) | 10 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Guérin-Méneville (1843) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Guillermet (2009) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Hagberg & Eriksson (2011) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Hassemer et al. (2016) | 10 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Hunt (1981) | 10 | 0.01% | 1 | 0% | 1 | 0% | 0 | 0% |
Jourde et al. (2017) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Karremans et al. (2020) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Kessler et al. (2011) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Kochanovski (2019) | 10 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Kulbicki et al. (2000) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 6 | 0.02% |
Kurina (2008) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Laurent & Kawahara (2019) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Lavocat Bernard & Reeb (2016) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Lelong et al. (2022) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Lourenço (2018) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Lucas et al. (2016) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Lucas (2012) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Lukhoba & Paton (2003) | 10 | 0.01% | 1 | 0% | 1 | 0% | 0 | 0% |
Mabille & Boullet (1917) | 10 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard (1978) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Marques (1988) | 10 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinez & Etienne (2002) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Massary et al. (2017) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 8 | 0.02% |
Masters et al. (2023) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Matesco & Grazia (2015) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Meyrick (1915) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Montrouzier (1860) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Norrbom et al. (2021) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Oliveira et al. (2019) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Olivier (1790-[1791]) | 10 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Opitz (2019) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Opitz (2021) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Papavero (1975) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Paulian (1982) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Pessoa & Alves (2018) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Prance (1986) | 10 | 0.01% | 8 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Rafinesque Schmaltz (1810) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Rasmussen & Gonzalez (2017) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Reis et al. (2003) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Remaudière & Etienne (1988) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Richard et al. (1982) | 10 | 0.01% | 4 | 0.01% | 4 | 0.01% | 3 | 0.01% |
Rogers & Ju (1998) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Romero-González et al. (2008) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Ruiz et al. (2019) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Sanborn (2023) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Sanborn (2024) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Santos & Aguiar (2013) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Santos et al. (2016) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Satthaphorn et al. (2023) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Sauer (1964) | 10 | 0.01% | 1 | 0% | 1 | 0% | 0 | 0% |
Short & Girón (2023) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
. Zoosystema, 42 (14): 195-205.">Silva & Pollet (2020) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Simon (1900) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Souza et al. (2022) | 10 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Swart (1942) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Tavakilian & Neouze (2004) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Tavakilian et al. (2007) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Touroult et al. (2012) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Trofimov et al. (2016) | 10 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Udulutsch et al. (2013) | 10 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Vilette & Aucourd (2024) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Vincent & Laguerre (2017) | 10 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Webster (2003) | 10 | 0.01% | 4 | 0.01% | 1 | 0% | 3 | 0.01% |
Wetterer (2002) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Wheeler (1932) | 10 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Wheeler (1936) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Whitehead et al. (1988) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Willemse (1985) | 10 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Wilson & Hunt (1967) | 10 | 0.01% | 10 | 0.03% | 10 | 0.03% | 10 | 0.03% |
Wood et al. (2015) | 10 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Adalsteinsson et al. (2009) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Allen et al. (2022) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Appelhans et al. (2021) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 7 | 0.02% |
Armada & Barra (1992) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Baranow & Szlachetko (2016) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Barbut (2016) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Béarez & Séret (2009) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Benavides & Hormiga (2016) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Berland (1924) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Blagoderov & Pollet (2020) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Boudrie et al. (2017) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Braet & Fretey (1997) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Brévignon (2021) | 9 | 0.01% | 6 | 0.02% | 3 | 0.01% | 6 | 0.02% |
Castroviejo-Fisher et al. (2011) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Chatzimanolis (2023) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Chaudoir (1872) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Coste et al. (2008) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Cowie (2000) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Cramer (1775) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Creao-duarte & Sakakibara (2016) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Curletti & Brûlé (2015) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Devecchi et al. (2018) | 9 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Dewynter et al. (2016) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Dierkens (2013) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Dusbabek & Lukoschus (1975) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Dyar & Knab (1906) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Dyar (1913) | 9 | 0.01% | 9 | 0.03% | 8 | 0.02% | 9 | 0.03% |
Fabricius (1781) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallen (1983) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Faynel & Robbins (2014) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Ferro & Marshall (2018) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Feuillet (2010) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Fontella Pereira & Brito de Goes (2009) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Fouque et al. (2007) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Fouquet et al. (2021) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Fouquet (2000) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Fragoso & Tavakilian (1985) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
França et al. (2024) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Gargominy & Muratov (2012) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Garrigues & Lamy (2019) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gentry (1980) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
, VI: 53-65.">Giuglaris (2012) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Gonzales (2023) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gordon (1975) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Gouda (2009) | 9 | 0.01% | 7 | 0.02% | 6 | 0.02% | 7 | 0.02% |
Gounelle (1909) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Gravier-Bonnet et al. (2007) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Gruhn et al. (2018) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Guillermet (2009) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Guth (1971) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 6 | 0.02% |
Hampson (1920) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Harvard University Museum & Morris P.J. (2020) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Hebard (1933) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Hemming (1958) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Herbin (2019) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Herbin (2021) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Herrmann et al. (2014) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Hübner (1816-[1826]) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Hübner ([1825-1831]) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Iamonico (2016) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Irmler (2016) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Irmler (2017) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Jourdan et al. (2014) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Jurberg et al. (2015) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Karremans (2015) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Kawasaki & Holst (1994) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Kimsey & Bohart (1990) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Kiszka et al. (2010) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 6 | 0.02% |
Labiak et al. (2015) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Laguerre (2016) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Laguerre (2019) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Laporte de Castelnau (1832) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Laurenti (1768) | 9 | 0.01% | 2 | 0.01% | 1 | 0% | 1 | 0% |
Lechat & Fournier (2017) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Lechat et al. (2022) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Ledoux & Hallé (1995) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Lèfevre (1876) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 5 | 0.02% |
Lemée (1956) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Leuenberger (1997) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Lewis & Oliver (1974) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Linnaeus (1759) | 9 | 0.01% | 3 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Loesener (1901) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Lukoschus et al. (1979) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Machordom et al. (2022) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Madison (1981) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Mantilleri (2015) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Marek (2015) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Marek (2016) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Matile-Ferrero et al. (2000) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Matile-Ferrero (1979) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 8 | 0.02% |
Mazur (1988) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Mederos & Pollet (2019) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Mendes et al. (2019) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Moraes-da-silva et al. (2021) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 5 | 0.02% |
Moure (1960) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Naviaux (1998) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 8 | 0.02% |
Nicolas (2012) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Nieser (1994) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Olmi et al. (2000) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Orejuela et al. (2017) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Ormerod (2007) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pádua et al. (2020) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Pessoa et al. (2018) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Pic (1926) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollard & Paton (2001) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Poncy (1996) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Proosdij (2007) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Redden et al. (2010) | 9 | 0.01% | 6 | 0.02% | 5 | 0.02% | 5 | 0.02% |
Reese & Mohamed (1985) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Rheinheimer (2012) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Rheinheimer (2021) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Richard (1792) | 9 | 0.01% | 1 | 0% | 1 | 0% | 0 | 0% |
Rider (1992) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Rome & Coppens d'Eeckenbrugge (2016) | 9 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Rubio & Rolán (2018) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Rudd (1987) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Sachet (1962) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sakuragui et al. (2018) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Sambin & Chiron (2014) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sambin & Chiron (2016) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sambin & Chiron (2017) | 9 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Schroers (2001) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Sepp (1848) | 9 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sharp (1882) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Shaughney & Ratcliffe (2015) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Shuey (2024) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Smith (1992) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Smith (2018) | 9 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sohn et al. (2015) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Song et al. (2019) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Soula (2006) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Spix (1825) | 9 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Straneo (1955) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Strohecker (1997) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Sukkharak & Gradstein (2017) | 9 | 0.01% | 4 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Sundell (1981) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Swallen (1964) | 9 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Swart & Queneherve (1998) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Taroda (1984) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Taylor et al. (2016) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Téllez-Valdés et al. (2019) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Theobald (1901) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Thiaucourt (1988) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Tillier (1980) | 9 | 0.01% | 2 | 0.01% | 1 | 0% | 2 | 0.01% |
Tippmann (1960) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Touroult et al. (2021) | 9 | 0.01% | 9 | 0.03% | 8 | 0.02% | 9 | 0.03% |
Touroult (2005) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 4 | 0.01% |
Tucker (2014) | 9 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Vasco et al. (2013) | 9 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Vorontsova et al. (2023) | 9 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Walker (1856) | 9 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Wenzel (1976) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Wolski et al. (2020) | 9 | 0.01% | 9 | 0.03% | 9 | 0.03% | 9 | 0.03% |
Adler et al. (2012) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Albertson & Dietrich (2005) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Albouy & Richard (2017) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Almeida & Santos (2014) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Amshoff (1951) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Anderson (1994) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Balazuc (1986) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Bayer et al. (2020) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Berland (1935) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Bésuchet (1982) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Bigot & Etienne (2009) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Bily (2017) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Borowiec (2000) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Bouchet et al. (1991) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Bourmaud (2003) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Bovini (2015) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Braet et al. (2003) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Braun et al. (1999) | 8 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Breton (2014) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Breuil (2009) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Brévignon (2000) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Brugnera et al. (2020) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Cardoso et al. (2020) | 8 | 0.01% | 8 | 0.02% | 5 | 0.02% | 6 | 0.02% |
Chatrou (1999) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Chovet et al. (2023) | 8 | 0.01% | 6 | 0.02% | 2 | 0.01% | 4 | 0.01% |
Clastrier (1970) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Cohen et al. (1990) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Comellini (1983) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Costa (1975) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Costa (2011) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Curletti & Brûlé (2016) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Cuvier & Valenciennes (1833) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Dalens et al. (2009) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Daly & Martínez-Habibe (2019) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Daly (2019) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
de Kort-Gommers & Nieser (1969) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 7 | 0.02% |
Degallier & Gomy (2024) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Degallier (2012) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Dewynter et al. (2016) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Dierkens & Charlat (2011) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Dognin (1907) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Du Puy et al. (1993) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Dubuisson et al. (2018) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Dulau-Drouot et al. (2008) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 4 | 0.01% |
Edmonds & Zidek (2010) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Emery (1896) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Evangelista et al. (2015) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Faynel et al. (2024) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Fernandes et al. (2000) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Fisch-Muller et al. (2012) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Fournier et al. (2017) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Freytag (2013) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Freytag (2018) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Fricke et al. (2013) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 7 | 0.02% |
Gallard & Salk (2019) | 8 | 0.01% | 7 | 0.02% | 4 | 0.01% | 7 | 0.02% |
Garrison & von Ellenrieder (2015) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Gery et al. (1996) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibeaux (2016) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Gibon (2019) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Gill (1995) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 5 | 0.02% |
Goldberg (1967) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Golvan (1962) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Gory (1833) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Grandcolas (1992) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Granjon et al. (2002) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 5 | 0.02% |
Gruhn et al. (2017) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Herrich-schäffer (1850-1858) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Herrmann et al. (2017) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Hill et al. (2006) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Irmler (2016) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Jameson (1996) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Khaustov & Frolov (2020) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Kohl (1902) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Konstantinov et al. (2022) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Kulbicki (comm. pers., 2011) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Külkamp et al. (2023) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Lachaud et al. (2012) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Lechat & Fournier (2019) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Léger et al. (2014) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Legros et al. (2017) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Lehtonen (2008) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Leraut (1988) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Lourenço et al. (2020) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Mantilleri (2015) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Marsh (2002) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Martin (2011) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Martins & Galileo (2007) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Martins & Monne (1980) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Martins (1969) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Meneguzzo (2020) | 8 | 0.01% | 3 | 0.01% | 0 | 0% | 3 | 0.01% |
Meyrick (1919) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Michaelsen (1913) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Monne (1985) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Monné (1988) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Moonlight et al. (2018) | 8 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Moreno (1993) | 8 | 0.01% | 6 | 0.02% | 3 | 0.01% | 3 | 0.01% |
Murray (1993) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Nakamura (1985) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Naviaux (2007) | 8 | 0.01% | 7 | 0.02% | 4 | 0.01% | 6 | 0.02% |
Nepal & Purintun (2021) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Nibouche et al. (202X) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Nicholson et al. (2012) | 8 | 0.01% | 7 | 0.02% | 6 | 0.02% | 5 | 0.02% |
O’Donnell et al. (2022) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Opitz (2015) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Orrico et al. (2017) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pastore et al. (2023) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Paulmier (2015) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Pennington (1997) | 8 | 0.01% | 5 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Peraza et al. (2022) | 8 | 0.01% | 7 | 0.02% | 5 | 0.02% | 4 | 0.01% |
Pessoa et al. (2015) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Platnick (1993) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Raynal (1974) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Réblová et al. (2020) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Reemer & Stahls (2013) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Reemer et al. (2019) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Regalado Gabancho & Prada (2011) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Reynolds & Henderson (2018) | 8 | 0.01% | 6 | 0.02% | 5 | 0.02% | 4 | 0.01% |
Rheinheimer (2010) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Rignault & Chevallier (2017) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Roguet (2023) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Rolston (1983) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Rome & Coppens d'Eeckenbrugge (2020) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Romero-González et al. (2015) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Rothschild (1909) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Sabroux et al. (2019) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sakakibara (2012) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Samaran & Guinet (2009) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 6 | 0.02% |
Sambin & Aucourd (2021) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Samson (2005) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Santos & Hoppe (2018) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Santos et al. (2023) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Sastre & Lescure (1978) | 8 | 0.01% | 3 | 0.01% | 3 | 0.01% | 3 | 0.01% |
Saussure (1857) | 8 | 0.01% | 2 | 0.01% | 2 | 0.01% | 2 | 0.01% |
Scataglini et al. (2014) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Scharf et al. (2006) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |
Scoble (1986) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Scoble (1990) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Soares et al. (2022) | 8 | 0.01% | 5 | 0.01% | 5 | 0.02% | 5 | 0.02% |
Soares Neto et al. (2018) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Somavilla et al. (2018) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 5 | 0.02% |
Soubeyran (2008) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Sousa & Sotuyo (2012) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Souza et al. (2010) | 8 | 0.01% | 1 | 0% | 1 | 0% | 1 | 0% |
Ståhl (2010) | 8 | 0.01% | 3 | 0.01% | 1 | 0% | 2 | 0.01% |
Sturaro et al. (2020) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Svenson (2014) | 8 | 0.01% | 7 | 0.02% | 7 | 0.02% | 7 | 0.02% |
Thériot et al. (1934) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiaucourt (1991) | 8 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Thulin et al. (2016) | 8 | 0.01% | 4 | 0.01% | 4 | 0.01% | 4 | 0.01% |
Touroult et al. (2010) | 8 | 0.01% | 8 | 0.02% | 8 | 0.02% | 8 | 0.02% |
Vaurie (1966) | 8 | 0.01% | 6 | 0.02% | 6 | 0.02% | 6 | 0.02% |