Coraux constructeurs de récifs
groupe paraphylétique regroupant l'ordre des Scleractinia, le genre Tubipora (corail orgue), l'espèce Heliopora coerulea (corail bleu) et la famille des Milleporidae (coraux de feu).
209 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Pichon (2007) | 313 | 16,47% | 232 | 26,45% | 232 | 26,58% | 232 | 26,58% |
| Pichon & Thomassin (2005) | 202 | 10,63% | 153 | 17,45% | 153 | 17,53% | 153 | 17,53% |
| Pichon et al. (2007) | 171 | 9% | 137 | 15,62% | 137 | 15,69% | 137 | 15,69% |
| Faure et al. (2008) | 162 | 8,52% | 133 | 15,17% | 133 | 15,23% | 133 | 15,23% |
| Glynn et al. (2007) | 149 | 7,84% | 117 | 13,34% | 117 | 13,4% | 117 | 13,4% |
| Kitahara (2011) | 119 | 6,26% | 118 | 13,45% | 116 | 13,29% | 118 | 13,52% |
| Tricart & Foubert (2000) | 105 | 5,52% | 88 | 10,03% | 88 | 10,08% | 86 | 9,85% |
| Cairns (1999) | 98 | 5,16% | 91 | 10,38% | 88 | 10,08% | 90 | 10,31% |
| Pichon (comm. pers., 2012) | 82 | 4,31% | 68 | 7,75% | 68 | 7,79% | 68 | 7,79% |
| Uicn et al. (2020) | 66 | 3,47% | 59 | 6,73% | 59 | 6,76% | 59 | 6,76% |
| Questel (2020) | 59 | 3,1% | 56 | 6,39% | 56 | 6,41% | 55 | 6,3% |
| Chevalier & Kuhlmann (1983) | 53 | 2,79% | 32 | 3,65% | 32 | 3,67% | 32 | 3,67% |
| Questel & Le Quellec (2012) | 52 | 2,74% | 44 | 5,02% | 44 | 5,04% | 43 | 4,93% |
| Dana (1846-1849) | 40 | 2,1% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Fenner & Muir (2008) | 40 | 2,1% | 34 | 3,88% | 34 | 3,89% | 34 | 3,89% |
| Andouche et al. (2020) | 38 | 2% | 36 | 4,1% | 36 | 4,12% | 36 | 4,12% |
| Diaz & Cuzange (2009) | 34 | 1,79% | 27 | 3,08% | 27 | 3,09% | 27 | 3,09% |
| Reveillaud et al. (2008) | 34 | 1,79% | 32 | 3,65% | 32 | 3,67% | 31 | 3,55% |
| Sheppard (1987) | 30 | 1,58% | 8 | 0,91% | 8 | 0,92% | 8 | 0,92% |
| Bigot (comm. pers., 2018) | 27 | 1,42% | 26 | 2,96% | 26 | 2,98% | 26 | 2,98% |
| Fautin (2013) | 22 | 1,16% | 22 | 2,51% | 21 | 2,41% | 21 | 2,41% |
| IUCN (2013) | 21 | 1,1% | 17 | 1,94% | 17 | 1,95% | 17 | 1,95% |
| Quelch (1886) | 20 | 1,05% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Gardiner (1899) | 19 | 1% | 9 | 1,03% | 9 | 1,03% | 9 | 1,03% |
| Flot & Adjeroud (2009) | 18 | 0,95% | 16 | 1,82% | 16 | 1,83% | 16 | 1,83% |
| Fourt et al. (2017) | 18 | 0,95% | 16 | 1,82% | 16 | 1,83% | 16 | 1,83% |
| Bosserelle et al. (2014) | 17 | 0,89% | 16 | 1,82% | 16 | 1,83% | 16 | 1,83% |
| AAMP (2010) | 15 | 0,79% | 15 | 1,71% | 14 | 1,6% | 15 | 1,72% |
| Kitahara & Cairns (2009) | 15 | 0,79% | 15 | 1,71% | 15 | 1,72% | 15 | 1,72% |
| Kitahara et al. (2010) | 15 | 0,79% | 15 | 1,71% | 15 | 1,72% | 15 | 1,72% |
| Orrell (2019) | 15 | 0,79% | 10 | 1,14% | 10 | 1,15% | 10 | 1,15% |
| Moseley ([1880]) | 14 | 0,74% | 7 | 0,8% | 7 | 0,8% | 7 | 0,8% |
| Ifremer (2009) | 13 | 0,68% | 10 | 1,14% | 10 | 1,15% | 9 | 1,03% |
| Low & Evenhuis (2013) | 13 | 0,68% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Duchassaing et al. (1864) | 12 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1968) | 12 | 0,63% | 8 | 0,91% | 8 | 0,92% | 8 | 0,92% |
| . Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 11 | 0,58% | 9 | 1,03% | 9 | 1,03% | 9 | 1,03% |
| National Institute of Water and Atmospheric Research (2016) | 10 | 0,53% | 7 | 0,8% | 7 | 0,8% | 7 | 0,8% |
| Payri et al. (2002) | 10 | 0,53% | 7 | 0,8% | 7 | 0,8% | 7 | 0,8% |
| Milne-Edwards (1848) | 9 | 0,47% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Peralta & Fautin (2013) | 9 | 0,47% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Adjeroud et al. (2012) | 8 | 0,42% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
| Arrigoni et al. (2016) | 8 | 0,42% | 8 | 0,91% | 8 | 0,92% | 8 | 0,92% |
| Cairns (2000) | 7 | 0,37% | 7 | 0,8% | 7 | 0,8% | 7 | 0,8% |
| Martin (2011) | 7 | 0,37% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
| Cairns (1989) | 6 | 0,32% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Cairns (2004) | 6 | 0,32% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Duchassaing et al. (1860) | 6 | 0,32% | 2 | 0,23% | 2 | 0,23% | 1 | 0,11% |
| Kitahara & Cairns (2008) | 6 | 0,32% | 6 | 0,68% | 6 | 0,69% | 6 | 0,69% |
| Pourtales (1868) | 6 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pourtalès (1880) | 6 | 0,32% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Zibrowius (1974) | 6 | 0,32% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 5 | 0,26% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Wells (1968) | 5 | 0,26% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Arrigoni et al. (2018) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Arrigoni et al. (2020) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Benzoni et al. (2010) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Goud et al. (2021) | 4 | 0,21% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Gravier-Bonnet et al. (2007) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Harvard University Museum & Morris P.J. (2020) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quelch (1884) | 4 | 0,21% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Uicn et al. (2019) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Vaughan (1906) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Volpi & Benvenuti (2003) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourcier (1988) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Bourmaud (2003) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Carricart-Ganivet & Reyes-Bonilla (1999) | 3 | 0,16% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Chevalier (1971) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Devantier et al. (2008) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gall (2021) | 3 | 0,16% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Gardiner (1897) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Gravier-Bonnet & Bourmaud (2005) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Hoffmeister (1929) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-Mer et al. (2011) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Johnston & Burgess (2023) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Nelson-Smith et al. (2014) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Vaughan (1907) | 3 | 0,16% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
| Tijdschrift der Nederlandse Dierkundige Vereeniging (Ser. 2), 7: 89-115.">Alcock (1902) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benzoni & Pichon (2004) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Benzoni et al. (2014) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Benzoni (2013) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Brook (1892) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns & Zibrowius (2016) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Cairns (1977) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Cairns (1979) | 2 | 0,11% | 2 | 0,23% | 1 | 0,11% | 2 | 0,23% |
| Cairns (1995) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Duchassaing & Fonbressin (1870) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis & Solander (1786) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forsskål (1775) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Gardiner (1900) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gravier-Bonnet (2007) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Hourigan (2020) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Ifremer (2020) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Sueur (1817) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindström (1877) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Linsley et al. (1999) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mckenna et al. (2009) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Richer de Forges et al. (2005) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Sheppard et al. (2008) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Turak et al. (2008) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Turak et al. (2014) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Umbgrove (1940) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veron (2000) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Wells (1961) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wijsman-Best (1970) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Yiu & Qiu (2022) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Zibrowius (1980) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Aronson et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arrigoni et al. (2016) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Australian Museum (2020) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Bernard (1896) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Bernard (1897) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Bernard (1897) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Boissin et al. (2019) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Brook (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (1979) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Cairns (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambert et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cecchini (1914) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Cuif et al. (2003) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Dennant (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Devantier et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Devantier et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| DORIS (2012) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Duchassaing & Fontbressin (1850) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Duncan (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duncan (1876) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Duncan (1889) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Fortic et al. (2023) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Gardiner (1898) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Goulletquer (2016) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Gravier (1910) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Gregory (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Head (1978) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema & Vicente (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Hoeksema et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema (2012) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| ICZN (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Julien (1881) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kayal & Kayal (2017) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Kitahara (2005) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Klunzinger (1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacaze-Duthiers (1897) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Linnaeus (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mckenna et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne & Edwards (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne et al. (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nemenzo (1976) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Nicet & Denis (2011) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Nolf & Cahuzac (2009) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Obura et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Owens (1994) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Payri et al. (2016) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Pichon et al. (2020) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Pourtalès (1874) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Pyle et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Richards et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Richards et al. (2014) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Risso (1826) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Roule (1900) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Schleyer & Benayahu (2016) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Sheppard et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Vaga et al. (2023) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Van et al. (2008) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Van Ofwegen (2007) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Veron & Wallace (1984) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Veron et al. (1977) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Veron (1985) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Veron (1985) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Verrill (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1872) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Verrill (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wallace & Wolstenholme (1998) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Wallace (1994) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Wallace (1999) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Yabe & Sugiyama (1937) | 1 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
| Zibrowius & Arnaud (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
