Conidae
228 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Héros et al. (2007) | 360 | 9,7% | 233 | 18,76% | 233 | 18,87% | 231 | 18,69% |
Lamy & Pointier (2018) | 354 | 9,54% | 280 | 22,54% | 280 | 22,67% | 280 | 22,65% |
Tröndlé & Boutet (2009) | 299 | 8,06% | 205 | 16,51% | 205 | 16,6% | 203 | 16,42% |
Jay et al. (2009) | 282 | 7,6% | 200 | 16,1% | 200 | 16,19% | 195 | 15,78% |
Bouchet et al. (2008) | 98 | 2,64% | 64 | 5,15% | 64 | 5,18% | 64 | 5,18% |
Deuss et al. (2013) | 74 | 1,99% | 41 | 3,3% | 40 | 3,24% | 40 | 3,24% |
Tardy & Stahlschmidt (2022) | 68 | 1,83% | 60 | 4,83% | 60 | 4,86% | 60 | 4,85% |
Fallon (2016) | 62 | 1,67% | 60 | 4,83% | 60 | 4,86% | 60 | 4,85% |
Massemin et al. (2009) | 48 | 1,29% | 30 | 2,42% | 30 | 2,43% | 30 | 2,43% |
Rabiller & Richard (2019) | 46 | 1,24% | 39 | 3,14% | 39 | 3,16% | 39 | 3,16% |
Richard et al. (1982) | 46 | 1,24% | 31 | 2,5% | 31 | 2,51% | 30 | 2,43% |
Deshayes (1863) | 44 | 1,19% | 17 | 1,37% | 17 | 1,38% | 17 | 1,38% |
Richard (2006) | 41 | 1,11% | 28 | 2,25% | 28 | 2,27% | 27 | 2,18% |
Fedosov et al. (2020) | 40 | 1,08% | 38 | 3,06% | 38 | 3,08% | 38 | 3,07% |
Ifremer (2009) | 38 | 1,02% | 31 | 2,5% | 31 | 2,51% | 31 | 2,51% |
Wells (1995) | 33 | 0,89% | 31 | 2,5% | 31 | 2,51% | 31 | 2,51% |
Chabanet et al. (2007) | 31 | 0,84% | 26 | 2,09% | 26 | 2,11% | 25 | 2,02% |
Tucker & Tenorio (2009) | 28 | 0,75% | 0 | 0% | 0 | 0% | 0 | 0% |
Röckel et al. (1995) | 27 | 0,73% | 9 | 0,72% | 9 | 0,73% | 9 | 0,73% |
Moolenbeek & Röckel (1996) | 25 | 0,67% | 13 | 1,05% | 13 | 1,05% | 13 | 1,05% |
Linnaeus (1758) | 23 | 0,62% | 22 | 1,77% | 22 | 1,78% | 22 | 1,78% |
Kilburn et al. (2014) | 22 | 0,59% | 22 | 1,77% | 22 | 1,78% | 22 | 1,78% |
Hedley (1922) | 20 | 0,54% | 14 | 1,13% | 14 | 1,13% | 14 | 1,13% |
Mulochau et al. (2020) | 20 | 0,54% | 19 | 1,53% | 19 | 1,54% | 18 | 1,46% |
Rabiller & Richard (2014) | 20 | 0,54% | 9 | 0,72% | 9 | 0,73% | 9 | 0,73% |
Moolenbeek et al. (2008) | 19 | 0,51% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Verneau (2007) | 17 | 0,46% | 15 | 1,21% | 15 | 1,21% | 15 | 1,21% |
Tenorio & Puillandre (2023) | 16 | 0,43% | 11 | 0,89% | 11 | 0,89% | 11 | 0,89% |
Boyer (2022) | 15 | 0,4% | 12 | 0,97% | 12 | 0,97% | 12 | 0,97% |
Kronen et al. (2008) | 15 | 0,4% | 15 | 1,21% | 15 | 1,21% | 15 | 1,21% |
Morassi et al. (2017) | 15 | 0,4% | 15 | 1,21% | 15 | 1,21% | 15 | 1,21% |
Reeve (1846) | 15 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2022) | 15 | 0,4% | 15 | 1,21% | 15 | 1,21% | 15 | 1,21% |
Zaharias et al. (2020) | 15 | 0,4% | 15 | 1,21% | 15 | 1,21% | 15 | 1,21% |
Gmelin (1791) | 14 | 0,38% | 12 | 0,97% | 12 | 0,97% | 12 | 0,97% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 14 | 0,38% | 12 | 0,97% | 12 | 0,97% | 12 | 0,97% |
Kantor et al. (2018) | 14 | 0,38% | 11 | 0,89% | 11 | 0,89% | 11 | 0,89% |
Boyer & Renda (2022) | 13 | 0,35% | 12 | 0,97% | 12 | 0,97% | 12 | 0,97% |
Kaiser (2009) | 13 | 0,35% | 11 | 0,89% | 11 | 0,89% | 11 | 0,89% |
Paulmier (2019) | 13 | 0,35% | 13 | 1,05% | 13 | 1,05% | 13 | 1,05% |
Petuch (1987) | 13 | 0,35% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Questel & Le Quellec (2012) | 13 | 0,35% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Motta (1982) | 12 | 0,32% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Questel (2020) | 12 | 0,32% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Fedosov & Puillandre (2012) | 10 | 0,27% | 10 | 0,81% | 10 | 0,81% | 10 | 0,81% |
Kantor et al. (2017) | 9 | 0,24% | 9 | 0,72% | 9 | 0,73% | 9 | 0,73% |
Pelorce & Hoarau (comm. pers., 2012) | 9 | 0,24% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Bouchet et al. (2022) | 8 | 0,22% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Cantera & Arnaud (1985) | 8 | 0,22% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Fedosov et al. (2017) | 8 | 0,22% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Hallan et al. (2021) | 8 | 0,22% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Melvill & Standen (1896) | 8 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Moolenbeek (1986) | 8 | 0,22% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Tenorio & Castelin (2016) | 8 | 0,22% | 8 | 0,64% | 8 | 0,65% | 8 | 0,65% |
Fedosov & Puillandre (2020) | 7 | 0,19% | 7 | 0,56% | 7 | 0,57% | 7 | 0,57% |
Hoarau (1998) | 7 | 0,19% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Kilburn et al. (2012) | 7 | 0,19% | 7 | 0,56% | 7 | 0,57% | 7 | 0,57% |
Powell (1960) | 7 | 0,19% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Schepman (1913) | 7 | 0,19% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Sysoev & Bouchet (1996) | 7 | 0,19% | 7 | 0,56% | 7 | 0,57% | 7 | 0,57% |
Sysoev & Bouchet (2001) | 7 | 0,19% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Terryn et al. (2019) | 7 | 0,19% | 7 | 0,56% | 7 | 0,57% | 7 | 0,57% |
Vergonzanne (1977) | 7 | 0,19% | 6 | 0,48% | 6 | 0,49% | 5 | 0,4% |
Wiedrick (2015) | 7 | 0,19% | 5 | 0,4% | 5 | 0,4% | 5 | 0,4% |
Delongueville & Scaillet (2020) | 6 | 0,16% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Pelorce & Horst (2020) | 6 | 0,16% | 6 | 0,48% | 6 | 0,49% | 6 | 0,49% |
Petuch (1979) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1983) | 6 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet & Sysoev (2001) | 5 | 0,13% | 5 | 0,4% | 5 | 0,4% | 5 | 0,4% |
Bratcher & Cernohorsky (1985) | 5 | 0,13% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Morassi & Bonfitto (2015) | 5 | 0,13% | 5 | 0,4% | 5 | 0,4% | 5 | 0,4% |
Puillandre et al. (2010) | 5 | 0,13% | 5 | 0,4% | 5 | 0,4% | 5 | 0,4% |
Puillandre et al. (2015) | 5 | 0,13% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Shikama (1970) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Shikama (1971) | 5 | 0,13% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Sowerby (1893) | 5 | 0,13% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Touitou et al. (2020) | 5 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bratcher & Cernohorsky (1982) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chino & Stahlschmidt (2014) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosse (1858) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Drivas & Jay (1986) | 4 | 0,11% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Fedosov (2011) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Héros (comm. pers., 2011) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Kantor & Puillandre (2021) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Kuroda (1956) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaer (2016) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier et al. (2018) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 4 | 0,11% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Preston (1908) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Puillandre et al. (2017) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Rehder (1980) | 4 | 0,11% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Richard & Moolenbeek (1988) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Stahlschmidt et al. (2022) | 4 | 0,11% | 4 | 0,32% | 4 | 0,32% | 4 | 0,32% |
Tenorio et al. (2018) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Amati et al. (2015) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Australian Museum (2020) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Bartsch & Rehder (1939) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bozzetti (2017) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bratcher (1981) | 3 | 0,08% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Dall & Simpson (1901) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1900) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Espinosa et al. (2017) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Godet et al. (2010) | 3 | 0,08% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Goud et al. (2020) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Habe (1965) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoarau & Pelorce (1998) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 2 | 0,16% |
Iredale (1931) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kosuge (1980) | 3 | 0,08% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Malcolm & Terryn (2012) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Melvill (1923) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Nordsieck (1977) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Petuch & Berschauer (2018) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pusateri et al. (2017) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Tenorio (2015) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Terryn & Lamy (2024) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Terryn (2021) | 3 | 0,08% | 3 | 0,24% | 3 | 0,24% | 3 | 0,24% |
Abdelkrim et al. (2018) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Aubry (2008) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Azuma (1972) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand & Clanzig (2019) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Bouchet & Sysoev (1997) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Bozzetti (1993) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Bozzetti (1994) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Bozzetti (1997) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chino (2006) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Conte (2023) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Criscione et al. (2021) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Crosse (1869) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Delsaerdt (1989) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Espinosa et al. (2017) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Espinosa et al. (2017) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Estival et al. (1986) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Fulton (1938) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Giannuzzi-savelli et al. (2018) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Habe & Kosuge (1970) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hervier (1897) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jousseaume (1883) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jousseaume (1884) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kantor et al. (2012) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Kilburn (1973) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Langeveld et al. (2020) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Locard & Caziot (1900-1901) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lum (2023) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaër (2012) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaër (2012) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaër (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaër (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaër (2019) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monteiro (2009) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Motta & Raybaudi (1992) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Motta (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Motta (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
American Journal of Conchology. 3(3): 211-222">Pease (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petuch (1979) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petuch (1980) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Powell (1958) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Puillandre et al. (2015) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Pusateri et al. (2017) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Raybaudi & Massilia (1992) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Richard & Rabiller (2013) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Rockel & Moolenbeek (1996) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rockel & Motta (1979) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rockel et al. (1993) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Stahlschmidt et al. (2012) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Tenorio (2015) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Terryn (2005) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tröndlé & Letourneux (2011) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Tröndlé et al. (2013) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Vink (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2001) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Watkins et al. (2010) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Wiedrick (2017) | 2 | 0,05% | 2 | 0,16% | 2 | 0,16% | 2 | 0,16% |
Wils & Delsaerdt (1989) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (1972) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Arnaud (1974) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Bartsch & Rehder (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1924) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dommergues & Dommergues (1998) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Duboc & Pineau (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Estival (1981) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Fehse (2011) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Journal of the Malacological Society of Australia, No. 5: 1-36.">Garrard (1961) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrard (1966) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaudiat & Violi (1977) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2020) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Iredale (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kantor & Fedosov (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kantor et al. (2016) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Kantor (2011) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Kilburn (1975) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2009) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Kronen et al. (2009) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Locard (1891) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Malcolm & Terryn (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Melvill (1898) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Melvill (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaud (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Tenorio (2005) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Monnier et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moolenbeek et al. (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moolenbeek (1993) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nappo et al. (2018) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Nicet & Denis (2011) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Pontier et al. (1987) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Powell (1969) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Puillandre et al. (2014) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Puillandre (2005) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Puillandre (2005) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Pusateri et al. (2016) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Röckel & Moolenbeek (1994) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Sander (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tenison Woods (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1987) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1989) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1993) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1993) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Terryn (1999) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Terryn (2001) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2005) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
The International Barcode of Life Consortium (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vink (1983) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |