Gastéropodes marins de Guadeloupe
215 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Lamy & Pointier (2018) | 2142 | 53,35% | 1865 | 131,43% | 1863 | 131,57% | 1861 | 131,43% |
Questel (2020) | 191 | 4,76% | 173 | 12,19% | 172 | 12,15% | 172 | 12,15% |
Questel & Le Quellec (2012) | 162 | 4,03% | 133 | 9,37% | 132 | 9,32% | 132 | 9,32% |
Massemin et al. (2009) | 151 | 3,76% | 114 | 8,03% | 114 | 8,05% | 113 | 7,98% |
Ortea et al. (2012) | 128 | 3,19% | 100 | 7,05% | 100 | 7,06% | 100 | 7,06% |
Cecalupo & Perugia (2020) | 87 | 2,17% | 83 | 5,85% | 83 | 5,86% | 83 | 5,86% |
Pelorce (2020) | 87 | 2,17% | 81 | 5,71% | 81 | 5,72% | 81 | 5,72% |
Ortea (2014) | 60 | 1,49% | 60 | 4,23% | 60 | 4,24% | 60 | 4,24% |
Espinosa & Ortea (2012) | 50 | 1,25% | 48 | 3,38% | 48 | 3,39% | 48 | 3,39% |
Fallon (2016) | 49 | 1,22% | 48 | 3,38% | 48 | 3,39% | 48 | 3,39% |
Ortea et al. (2018) | 48 | 1,2% | 39 | 2,75% | 39 | 2,75% | 39 | 2,75% |
Rabiller & Richard (2019) | 46 | 1,15% | 39 | 2,75% | 39 | 2,75% | 39 | 2,75% |
Tröndlé & Boutet (2009) | 43 | 1,07% | 31 | 2,18% | 31 | 2,19% | 30 | 2,12% |
Jay et al. (2009) | 42 | 1,05% | 18 | 1,27% | 18 | 1,27% | 18 | 1,27% |
Ortea (2015) | 42 | 1,05% | 42 | 2,96% | 42 | 2,97% | 42 | 2,97% |
Garrigues & Lamy (2019) | 36 | 0,9% | 34 | 2,4% | 34 | 2,4% | 34 | 2,4% |
Gmelin (1791) | 33 | 0,82% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 33 | 0,82% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Ortea et al. (2013) | 31 | 0,77% | 15 | 1,06% | 15 | 1,06% | 15 | 1,06% |
Héros et al. (2007) | 29 | 0,72% | 15 | 1,06% | 15 | 1,06% | 14 | 0,99% |
Garrigues et al. (2022) | 27 | 0,67% | 27 | 1,9% | 27 | 1,91% | 27 | 1,91% |
Paulmier (2015) | 27 | 0,67% | 25 | 1,76% | 25 | 1,77% | 25 | 1,77% |
Paulmier (2017) | 24 | 0,6% | 22 | 1,55% | 22 | 1,55% | 22 | 1,55% |
Petuch (1987) | 24 | 0,6% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Espinosa & Ortea (2013) | 22 | 0,55% | 22 | 1,55% | 22 | 1,55% | 22 | 1,55% |
Bidgrain (2015) | 19 | 0,47% | 15 | 1,06% | 15 | 1,06% | 15 | 1,06% |
Garrigues & Merle (2014) | 18 | 0,45% | 16 | 1,13% | 16 | 1,13% | 16 | 1,13% |
Deshayes (1863) | 16 | 0,4% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Kaiser (2009) | 16 | 0,4% | 10 | 0,7% | 9 | 0,64% | 10 | 0,71% |
Bouchet et al. (2008) | 15 | 0,37% | 9 | 0,63% | 9 | 0,64% | 9 | 0,64% |
Deuss et al. (2013) | 13 | 0,32% | 11 | 0,78% | 11 | 0,78% | 11 | 0,78% |
Linnaeus (1758) | 13 | 0,32% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Fedosov et al. (2020) | 10 | 0,25% | 10 | 0,7% | 10 | 0,71% | 10 | 0,71% |
Nelson-Smith et al. (2014) | 10 | 0,25% | 8 | 0,56% | 8 | 0,56% | 8 | 0,56% |
Rubio & Rolán (2015) | 9 | 0,22% | 9 | 0,63% | 9 | 0,64% | 9 | 0,64% |
Rubio et al. (2015) | 9 | 0,22% | 9 | 0,63% | 9 | 0,64% | 9 | 0,64% |
Sowerby (1844) | 9 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2011) | 8 | 0,2% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Richard et al. (1982) | 8 | 0,2% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Delannoye et al. (2015) | 7 | 0,17% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Garrigues & Lamy (2018) | 7 | 0,17% | 7 | 0,49% | 7 | 0,49% | 7 | 0,49% |
Paulmier (2019) | 7 | 0,17% | 7 | 0,49% | 7 | 0,49% | 7 | 0,49% |
Tucker & Tenorio (2009) | 7 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Espinosa & Ortea (2017) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fehse & Simone (2020) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Ortea & Espinosa (2016) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Ortea (2023) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Ortea (2023) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Pelorce (2017) | 6 | 0,15% | 5 | 0,35% | 5 | 0,35% | 5 | 0,35% |
Poppe et al. (2023) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Rubio & Rolán (2018) | 6 | 0,15% | 6 | 0,42% | 6 | 0,42% | 6 | 0,42% |
Caziot (1921) | 5 | 0,12% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Couto et al. (2016) | 5 | 0,12% | 5 | 0,35% | 5 | 0,35% | 5 | 0,35% |
Ghanimi et al. (2020) | 5 | 0,12% | 5 | 0,35% | 5 | 0,35% | 5 | 0,35% |
Ifremer (2009) | 5 | 0,12% | 5 | 0,35% | 5 | 0,35% | 5 | 0,35% |
Richard (2006) | 5 | 0,12% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Touitou et al. (2020) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall & Simpson (1901) | 4 | 0,1% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Faber & Moolenbeek (2013) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Fedosov et al. (2018) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Feliciano et al. (2021) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Houart & Garrigues (2023) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Hovestadt & Neckheim (2020) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Michenet & Bosserelle (2013) | 4 | 0,1% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Monnier & Limpalaer (2016) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulmier (2007) | 4 | 0,1% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Rehder (1943) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rolán & Fernández-Garcés (2015) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Strong et al. (2017) | 4 | 0,1% | 4 | 0,28% | 4 | 0,28% | 4 | 0,28% |
Bouchet & Pointier (1998) | 3 | 0,07% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Boyer (2003) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Bozzetti (2017) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg (1900) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
García-Méndez et al. (2022) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Garrigues & Lamy (2017) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Garrigues (2021) | 3 | 0,07% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Garriques & Lamy (2017) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Hervé (2010) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Krug et al. (2018) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Michel et al. (1971) | 3 | 0,07% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Mulochau et al. (2020) | 3 | 0,07% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Avicennia, 20: 21-22.">Ortea & Espinosa (2017) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Ortea et al. (2014) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (2015) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Ortea (2023) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Pelorce & Hoarau (comm. pers., 2012) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 3 | 0,07% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Rubio & Rolán (2017) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Sanders et al. (2017) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Terryn & Lamy (2024) | 3 | 0,07% | 3 | 0,21% | 3 | 0,21% | 3 | 0,21% |
Turton (1932) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Baba (1959) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Blanchard (2009) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Boyer & Lamy (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bozzetti (2010) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Caballer & Ortea (2014) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Caballer & Ortea (2015) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Caballer & Ortea (2015) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Caballer & Ortea (2019) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Chabanet et al. (2007) | 2 | 0,05% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Coomans (1967) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dautzenberg & Fischer (1906) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Espinosa & Ortea (2013) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Espinosa & Ortea (2013) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Espinosa et al. (2017) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Espinosa et al. (2017) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Faber & Moolenbeek (2014) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Faber (2013) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Faber (2019) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Fehse (2022) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Fengshan (1989) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraussen & Hadorn (2005) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 2 | 0,05% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Harasewych et al. (2020) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Houart (2002) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Huang et al. (2020) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Iredale (1931) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kantor et al. (2020) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Krug et al. (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorenz (2002) | 2 | 0,05% | 2 | 0,14% | 0 | 0% | 2 | 0,14% |
Lyons & Snyder (2019) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Moolenbeek & Faber (1991) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Motta & Raybaudi (1992) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Motta (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea & Moro (2016) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Ortea (2020) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Ortea (2023) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Ortea (2023) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Ortea (2023) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Paulmier (1997) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulmier (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelorce & Faber (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelorce (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit & Harasewych (2011) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Petuch (1980) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Petuch (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontier et al. (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Puillandre et al. (2015) | 2 | 0,05% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Risbec (1928) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1818) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schilder (1933) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stahlschmidt et al. (2012) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Strong & Bouchet (2020) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Terryn (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Verrill & Bush (1900) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Vilvens (2001) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Vink (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Watters & Fraussen (2015) | 2 | 0,05% | 2 | 0,14% | 2 | 0,14% | 2 | 0,14% |
Azuma (1960) | 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 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bertrand & Clanzig (2019) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bouchet & Kantor (2000) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bouchet & Waren (1986) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bouchet et al. (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet et al. (2022) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bourcier (1988) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Bourjon et al. (2018) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Boyer (2023) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Breton (2014) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Brugneaux & Pérès (2005) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Brustel & Touitou (2024) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Cantera & Arnaud (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cate (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dall (1925) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delongueville & Scaillet (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewarumez et al. (2011) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
DORIS (2012) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Dragicevic et al. (2019) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Egger et al. (2020) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Fassio et al. (2022) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Fedosov et al. (2017) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraussen & Stahlschmidt (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaudiat & Violi (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Golestani et al. (2019) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Goulletquer (2016) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Grall et al. (2015) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Guilding (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harry (1967) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoarau & Pelorce (1998) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Houard et al. (2019) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Houart et al. (2021) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Iredale (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kantor et al. (2018) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Kronen et al. (2008) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Linnaeus (1767) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Marcus (1955) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Mcginty (1940) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2017) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Oliverio (2003) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Ortea et al. (2014) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Ortea et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea (2017) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Ortea (2020) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Ortea (2022) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Parenzan (1970) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parth (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petuch (2002) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Pointier (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeve (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rubio & Rolàn (2014) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Sander (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Procès-Verbaux de la Société Linnéenne de Bordeaux, 79: 48.">Sigalas (1927) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Snyder (2007) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Sumner-rooney et al. (2016) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Tardy (2015) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Valdés (2008) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Watson (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Watters (2011) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |
Yokoyama (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zinke et al. (2005) | 1 | 0,02% | 1 | 0,07% | 1 | 0,07% | 1 | 0,07% |