Gastéropodes marins de Mayotte
203 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Jay et al. (2009) | 635 | 14,56% | 325 | 31,43% | 322 | 31,94% | 321 | 31,78% |
Héros et al. (2007) | 571 | 13,09% | 385 | 37,23% | 385 | 38,19% | 370 | 36,63% |
Tröndlé & Boutet (2009) | 476 | 10,91% | 317 | 30,66% | 317 | 31,45% | 308 | 30,5% |
Deuss et al. (2013) | 438 | 10,04% | 295 | 28,53% | 287 | 28,47% | 293 | 29,01% |
Bidgrain (2015) | 314 | 7,2% | 227 | 21,95% | 227 | 22,52% | 227 | 22,48% |
Deshayes (1863) | 178 | 4,08% | 39 | 3,77% | 39 | 3,87% | 38 | 3,76% |
Richard et al. (1982) | 156 | 3,58% | 87 | 8,41% | 87 | 8,63% | 79 | 7,82% |
Richard (2006) | 135 | 3,09% | 83 | 8,03% | 83 | 8,23% | 78 | 7,72% |
Chabanet et al. (2007) | 88 | 2,02% | 49 | 4,74% | 49 | 4,86% | 48 | 4,75% |
Pelorce & Hoarau (comm. pers., 2012) | 83 | 1,9% | 40 | 3,87% | 40 | 3,97% | 40 | 3,96% |
Linnaeus (1758) | 80 | 1,83% | 20 | 1,93% | 20 | 1,98% | 19 | 1,88% |
Lamy & Pointier (2018) | 74 | 1,7% | 67 | 6,48% | 67 | 6,65% | 67 | 6,63% |
Cecalupo & Perugia (2021) | 54 | 1,24% | 49 | 4,74% | 49 | 4,86% | 49 | 4,85% |
Kronen et al. (2008) | 40 | 0,92% | 30 | 2,9% | 30 | 2,98% | 30 | 2,97% |
Mulochau et al. (2020) | 40 | 0,92% | 37 | 3,58% | 36 | 3,57% | 36 | 3,56% |
Cernohorsky (1981) | 39 | 0,89% | 29 | 2,8% | 29 | 2,88% | 29 | 2,87% |
Gmelin (1791) | 35 | 0,8% | 9 | 0,87% | 9 | 0,89% | 9 | 0,89% |
Kaiser (2009) | 35 | 0,8% | 23 | 2,22% | 23 | 2,28% | 21 | 2,08% |
Michenet & Bosserelle (2013) | 34 | 0,78% | 29 | 2,8% | 29 | 2,88% | 29 | 2,87% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 32 | 0,73% | 9 | 0,87% | 9 | 0,89% | 9 | 0,89% |
Vachon & Verneau (2008) | 32 | 0,73% | 19 | 1,84% | 11 | 1,09% | 15 | 1,49% |
Drivas & Jay (1997) | 30 | 0,69% | 23 | 2,22% | 23 | 2,28% | 23 | 2,28% |
Fedosov et al. (2018) | 29 | 0,66% | 29 | 2,8% | 29 | 2,88% | 29 | 2,87% |
Hervé (2010) | 29 | 0,66% | 19 | 1,84% | 19 | 1,88% | 19 | 1,88% |
Vergonzanne (1977) | 19 | 0,44% | 9 | 0,87% | 9 | 0,89% | 8 | 0,79% |
Vannozzi (2023) | 17 | 0,39% | 17 | 1,64% | 17 | 1,69% | 17 | 1,68% |
Verneau (2007) | 17 | 0,39% | 15 | 1,45% | 15 | 1,49% | 15 | 1,49% |
Risbec (1928) | 16 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 14 | 0,32% | 12 | 1,16% | 12 | 1,19% | 12 | 1,19% |
Bouchet et al. (2008) | 13 | 0,3% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Jay & Drivas (2002) | 12 | 0,28% | 4 | 0,39% | 4 | 0,4% | 4 | 0,4% |
Zaharias et al. (2020) | 11 | 0,25% | 11 | 1,06% | 11 | 1,09% | 11 | 1,09% |
Fedosov et al. (2020) | 10 | 0,23% | 10 | 0,97% | 10 | 0,99% | 10 | 0,99% |
Monsecour & Monsecour (2018) | 10 | 0,23% | 10 | 0,97% | 10 | 0,99% | 10 | 0,99% |
Questel & Le Quellec (2012) | 10 | 0,23% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Bourjon et al. (2018) | 9 | 0,21% | 9 | 0,87% | 9 | 0,89% | 9 | 0,89% |
Griffiths & Florens (2006) | 9 | 0,21% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Nicet & Denis (2011) | 9 | 0,21% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Hoarau & Pelorce (1998) | 8 | 0,18% | 5 | 0,48% | 5 | 0,5% | 5 | 0,5% |
Hoarau (1998) | 8 | 0,18% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Ortea et al. (2012) | 8 | 0,18% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Rubio & Rolán (2022) | 8 | 0,18% | 8 | 0,77% | 8 | 0,79% | 8 | 0,79% |
Sanders et al. (2017) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Zinke et al. (2005) | 8 | 0,18% | 7 | 0,68% | 7 | 0,69% | 7 | 0,69% |
Moolenbeek & Röckel (1996) | 7 | 0,16% | 7 | 0,68% | 7 | 0,69% | 7 | 0,69% |
Franc (1956) | 6 | 0,14% | 6 | 0,58% | 6 | 0,6% | 6 | 0,59% |
Iredale (1931) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Massemin et al. (2009) | 6 | 0,14% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Motta (1982) | 6 | 0,14% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Wantiez (2001) | 6 | 0,14% | 3 | 0,29% | 3 | 0,3% | 2 | 0,2% |
Cecalupo & Perugia (2014) | 5 | 0,11% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Cecalupo & Perugia (2017) | 5 | 0,11% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Laseron (1956) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Marshall (1983) | 5 | 0,11% | 5 | 0,48% | 5 | 0,5% | 5 | 0,5% |
Cecalupo & Robba (2010) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1884) | 4 | 0,09% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Iredale (1936) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 4 | 0,09% | 4 | 0,39% | 4 | 0,4% | 4 | 0,4% |
Rudman (1982) | 4 | 0,09% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Tucker & Tenorio (2009) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Brook (2010) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Cecalupo & Perugia (2023) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Donohoo et al. (2023) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Geiger & Sasaki (2008) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Geiger (2012) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Houart (1985) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Jousseaume (1884) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2009) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Kronen et al. (2009) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Kronenberg (2015) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Krug et al. (2018) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Maxwell et al. (2021) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Morelet (1881) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Nelson-Smith et al. (2014) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Petuch & Berschauer (2018) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pizzini et al. (2013) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Pola et al. (2008) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Preston (1908) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Rubio & Rolán (2019) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Rudman (1990) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Salvat & Bacchet (2011) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Tibiriçá et al. (2023) | 3 | 0,07% | 3 | 0,29% | 3 | 0,3% | 3 | 0,3% |
Turton (1932) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 3 | 0,07% | 3 | 0,29% | 2 | 0,2% | 3 | 0,3% |
Vachon & Verneau (2017) | 3 | 0,07% | 3 | 0,29% | 0 | 0% | 3 | 0,3% |
Wilson & Burghardt (2015) | 3 | 0,07% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Adams (1853) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud et al. (2002) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beu (1986) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beu (1998) | 2 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Bouchet & Snyder (2013) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Bratcher & Cernohorsky (1982) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bratcher (1981) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Carmona et al. (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Cauvin (2005) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Cauvin (2007) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Cauvin (2010) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Cauvin (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Crosse (1858) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Drivas & Jay (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fedosov et al. (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Fehse & Grego (2002) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Fehse (2017) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Fraussen & Vermeij (2021) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Frydman (2000) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1871) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Héros (comm. pers., 2011) | 2 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Houard et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Houart & Heros (2015) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Houart & Vilvens (1997) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Jenkins & Köhler (2024) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Jousseaume (1874) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lima et al. (2016) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Marie (1869) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monnier & Limpalaer (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Motta (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea (1982) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Philippi (1842-1850) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pizzini & Raines (2011) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Poppe et al. (2023) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Pruvot-Fol (1930) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabiller & Richard (2019) | 2 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Reeve (1844-1845) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rehder (1980) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenberg & Salisbury (2014) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Rubio & Rolán (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Rubio et al. (2019) | 2 | 0,05% | 2 | 0,19% | 2 | 0,2% | 2 | 0,2% |
Starmühlner (1970) | 2 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Terryn (2005) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vilvens (2006) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Abdelkrim et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Abdou et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartsch & Rehder (1939) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bazzicalupo et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Beu et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyer (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Cate (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Cecalupo & Perugia (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Cernohorsky (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Clench & Turner (1948) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Couto et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Dragicevic et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Duboc & Pineau (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fassio et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Fedosov & Puillandre (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Fedosov et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Fraussen et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Garrard (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrett (1879) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Garrett (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassies (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Geiger (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Geiger (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Geiger (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Golestani et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Goulletquer (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Gout (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Habe & Kosuge (1966) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Habe & Kosuge (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Helbling (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Innabi et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Kantor & Fedosov (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilburn (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kira (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kool (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Kool (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Kronenberg (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorenz & Fehse (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Malaquias et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Michel et al. (1971) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Odhner (1919) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1915) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Paulmier (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Petuch (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pola et al. (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Pontier et al. (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prati & Musetti (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Preston (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reid & Kaiser (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 0 | 0% |
Richard (1985) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Rudman (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schepman (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shikama (1970) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Snyder & Bouchet (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Solem (1961) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Sowerby (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tardy & Stahlschmidt (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Tenorio et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
. Rapport G.I.S. "Lag-May", Mayotte & C.O.M. Marseille. 34 pp.">Thomassin (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Valdés (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Verneau (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
Viader (1951) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yonow (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |