Astéries
Asteroidea
219 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Sladen (1889) | 69 | 4,63% | 21 | 4,51% | 17 | 3,81% | 15 | 3,36% |
| Ducarme (2023) | 63 | 4,23% | 63 | 13,52% | 63 | 14,13% | 61 | 13,68% |
| Améziane (2007) | 57 | 3,83% | 51 | 10,94% | 51 | 11,43% | 50 | 11,21% |
| Ameziane et al. (2020) | 37 | 2,48% | 32 | 6,87% | 31 | 6,95% | 32 | 7,17% |
| Dilman (2014) | 37 | 2,48% | 36 | 7,73% | 36 | 8,07% | 33 | 7,4% |
| Ifremer (2009) | 36 | 2,42% | 26 | 5,58% | 26 | 5,83% | 24 | 5,38% |
| Martin (2011) | 36 | 2,42% | 32 | 6,87% | 30 | 6,73% | 30 | 6,73% |
| Guille et al. (1986) | 33 | 2,22% | 31 | 6,65% | 31 | 6,95% | 30 | 6,73% |
| Arnaud (1974) | 28 | 1,88% | 24 | 5,15% | 21 | 4,71% | 24 | 5,38% |
| Clark & Rowe (1971) | 24 | 1,61% | 23 | 4,94% | 23 | 5,16% | 23 | 5,16% |
| Jangoux & Aziz (1988) | 23 | 1,54% | 21 | 4,51% | 20 | 4,48% | 21 | 4,71% |
| Koehler (1921) | 23 | 1,54% | 18 | 3,86% | 18 | 4,04% | 16 | 3,59% |
| Nelson-Smith et al. (2014) | 23 | 1,54% | 16 | 3,43% | 16 | 3,59% | 14 | 3,14% |
| Mah (2017) | 20 | 1,34% | 20 | 4,29% | 20 | 4,48% | 20 | 4,48% |
| Mah (2018) | 20 | 1,34% | 20 | 4,29% | 20 | 4,48% | 20 | 4,48% |
| Danis & Jangoux (2008) | 16 | 1,07% | 13 | 2,79% | 13 | 2,91% | 12 | 2,69% |
| Marsh (1974) | 16 | 1,07% | 16 | 3,43% | 16 | 3,59% | 15 | 3,36% |
| Smith (1876) | 15 | 1,01% | 4 | 0,86% | 4 | 0,9% | 0 | 0% |
| Cherbonnier & Guille (1975) | 14 | 0,94% | 12 | 2,58% | 9 | 2,02% | 11 | 2,47% |
| Conand et al. (2018) | 14 | 0,94% | 14 | 3% | 14 | 3,14% | 13 | 2,91% |
| Fourt et al. (2017) | 14 | 0,94% | 14 | 3% | 14 | 3,14% | 12 | 2,69% |
| Micael et al. (2012) | 13 | 0,87% | 12 | 2,58% | 12 | 2,69% | 12 | 2,69% |
| Paulay & Brown (2019) | 13 | 0,87% | 12 | 2,58% | 12 | 2,69% | 12 | 2,69% |
| Walenkamp (1979) | 13 | 0,87% | 11 | 2,36% | 11 | 2,47% | 10 | 2,24% |
| Orrell (2019) | 12 | 0,81% | 11 | 2,36% | 11 | 2,47% | 11 | 2,47% |
| Conand & ARVAM (2005) | 11 | 0,74% | 11 | 2,36% | 11 | 2,47% | 11 | 2,47% |
| Dilman (2013) | 11 | 0,74% | 9 | 1,93% | 9 | 2,02% | 8 | 1,79% |
| Mah (2021) | 10 | 0,67% | 10 | 2,15% | 10 | 2,24% | 10 | 2,24% |
| Sladen (1882) | 10 | 0,67% | 5 | 1,07% | 5 | 1,12% | 4 | 0,9% |
| Arnaud (1964) | 8 | 0,54% | 8 | 1,72% | 7 | 1,57% | 8 | 1,79% |
| Perrier (1881) | 8 | 0,54% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Conand et al. (2016) | 7 | 0,47% | 7 | 1,5% | 7 | 1,57% | 7 | 1,57% |
| Milne-edwards (1882) | 7 | 0,47% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Brugneaux & Pibot (2012) | 6 | 0,4% | 5 | 1,07% | 4 | 0,9% | 5 | 1,12% |
| Clark (1996) | 6 | 0,4% | 6 | 1,29% | 3 | 0,67% | 6 | 1,35% |
| Linnaeus (1758) | 6 | 0,4% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2005) | 6 | 0,4% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Mah (2006) | 6 | 0,4% | 4 | 0,86% | 4 | 0,9% | 4 | 0,9% |
| Bollard et al. (2013) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Bourcier (1988) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Harvard University Museum & Morris P.J. (2020) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Mah et al. (2014) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Mills et al. (2018) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| O'loughlin & Rowe (2006) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Perrier (1875) | 5 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 5 | 0,34% | 5 | 1,07% | 5 | 1,12% | 5 | 1,12% |
| Studer (1876) | 5 | 0,34% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bocquet (1953) | 4 | 0,27% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Bourmaud (2003) | 4 | 0,27% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Chagnoux (2022) | 4 | 0,27% | 4 | 0,86% | 4 | 0,9% | 4 | 0,9% |
| Ludwig (1905) | 4 | 0,27% | 4 | 0,86% | 4 | 0,9% | 4 | 0,9% |
| Müller & Troschel (1842) | 4 | 0,27% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Thomson (1873) | 4 | 0,27% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Downey (1986) | 3 | 0,2% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Godet et al. (2010) | 3 | 0,2% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Hardouin Michelin (1844) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Korzhavina & Ivanenko (2019) | 3 | 0,2% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Müller (1776) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| O'Loughlin & MacKenzie (2013) | 3 | 0,2% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Parelius (1768) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pawson et al. (2009) | 3 | 0,2% | 3 | 0,64% | 2 | 0,45% | 3 | 0,67% |
| Pennant (1777) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1875) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1885) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1894) | 3 | 0,2% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Philippi (1837) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauvage (1890) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wantiez (2001) | 3 | 0,2% | 3 | 0,64% | 3 | 0,67% | 3 | 0,67% |
| Amon et al. (2017) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Calabuig (2016) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Chabanet et al. (2007) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Clark (1967) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Collectif & Bebest (2019) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Fau (2024) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Gadeau de Kerville (1900) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haszprunar & Spies (2014) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jangoux (1981) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Koehler (1907) | 2 | 0,13% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Koehler (1920) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kronen et al. (2008) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Mah (2003) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Mah (2007) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Mah (2015) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Mah (2024) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Monod & Dollfus (1932) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Natural History Museum of London (2020) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| O'loughlin & Bribiesca-contreras (2017) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Perrier (1891) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Questel & Le Quellec (2012) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Rignault & Chevallier (2017) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Sars (1861) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Sibuet (1974) | 2 | 0,13% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Sibuet (1976) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Sladen (1883) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| Sladen (1891) | 2 | 0,13% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Solís-Marín & Laguarda Figueras (2009) | 2 | 0,13% | 2 | 0,43% | 2 | 0,45% | 2 | 0,45% |
| . London: Macmillan. 1: 1-424. 2: 1-396. ">Thomson (1878) |
2 | 0,13% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Verrill (1876) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asbjornsen (1856) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Australian Museum (2020) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bell (1917) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (2006) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Breton (2014) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Brugneaux & Pérès (2006) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Bruzelius (1805) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cherbonnier (1970) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Clark & Mcknight (2001) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Clark (1923) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clark (1948) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Coleman (1911) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand et al. (2013) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Conand et al. (2016) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Crosnier (1959) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Dartnall (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Dartnall (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Diaz & Cuzange (2009) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Doderlein (1917) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Downey (1973) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Downey (1986) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Düben & Koren (1846) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Düben (1845) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Ducarme (2023) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Emson & Crump (1979) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Escoubet (1984) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| European Nucleotide Archive (2019) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Fenaux (1965) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Fisher (1906) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fisher (1910) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fisher (1916) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fisher (1940) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Gasco (1876) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gondim et al. (2014) | 1 | 0,07% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| Haszprunar et al. (2017) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Humes (1976) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Ifremer (2023) | 1 | 0,07% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
| . Annales de l'Université de Lyon. 26: 33-127, pls. I-IV.">Koehler (1896) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Koehler (1906) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Koehler (1907) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koehler (1912) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1816) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linné (1771) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ludwig (1907) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2008) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2018) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2020) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2023) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Mah (2023) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2023) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Marenzeller & Von (1893) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël (2017) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Perrier (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1885) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi de (1859) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1870) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prato & Pastore (2012) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Pyle et al. (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Retzius (1783) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sars (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sibuet (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sigovini & Tagliapietra (2009) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Sladen (1883) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stampanato & Jangoux (1993) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stampanato & Jangoux (2004) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 0 | 0% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Stampanato (2015) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Vázquez Bader & Gracia G. (1994) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Vergonzanne (1977) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Verrill (1882) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1915) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vincent et al. (2004) | 1 | 0,07% | 1 | 0,21% | 1 | 0,22% | 1 | 0,22% |
| Zilli (2021) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
