Cnidaires
Cnidaria
626 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 | 5.21% | 232 | 8.21% | 232 | 8.24% | 232 | 8.24% |
Pichon & Thomassin (2005) | 202 | 3.36% | 153 | 5.41% | 153 | 5.43% | 153 | 5.43% |
Van Ofwegen (2007) | 172 | 2.87% | 153 | 5.41% | 153 | 5.43% | 153 | 5.43% |
Pichon et al. (2007) | 171 | 2.85% | 137 | 4.85% | 137 | 4.86% | 137 | 4.86% |
Faure et al. (2008) | 163 | 2.72% | 134 | 4.74% | 134 | 4.76% | 134 | 4.76% |
Cairns (2015) | 162 | 2.7% | 158 | 5.59% | 158 | 5.61% | 158 | 5.61% |
Ifremer (2009) | 150 | 2.5% | 138 | 4.88% | 138 | 4.9% | 137 | 4.86% |
Glynn et al. (2007) | 149 | 2.48% | 117 | 4.14% | 117 | 4.15% | 117 | 4.15% |
Philippot (1987) | 121 | 2.02% | 106 | 3.75% | 105 | 3.73% | 104 | 3.69% |
Kitahara (2011) | 119 | 1.98% | 118 | 4.18% | 116 | 4.12% | 118 | 4.19% |
Andouche et al. (2020) | 108 | 1.8% | 96 | 3.4% | 96 | 3.41% | 96 | 3.41% |
Tricart & Foubert (2000) | 108 | 1.8% | 91 | 3.22% | 91 | 3.23% | 89 | 3.16% |
Grasshoff (1999) | 107 | 1.78% | 97 | 3.43% | 97 | 3.44% | 97 | 3.44% |
Questel (2020) | 105 | 1.75% | 100 | 3.54% | 100 | 3.55% | 99 | 3.51% |
Nelson-Smith et al. (2014) | 102 | 1.7% | 83 | 2.94% | 83 | 2.95% | 81 | 2.88% |
Gravier-Bonnet (2007) | 101 | 1.68% | 86 | 3.04% | 86 | 3.05% | 86 | 3.05% |
Cairns (1999) | 98 | 1.63% | 91 | 3.22% | 88 | 3.12% | 90 | 3.19% |
Vervoort (1993) | 98 | 1.63% | 87 | 3.08% | 87 | 3.09% | 87 | 3.09% |
Bourmaud (2003) | 97 | 1.62% | 71 | 2.51% | 71 | 2.52% | 71 | 2.52% |
Questel & Le Quellec (2012) | 96 | 1.6% | 80 | 2.83% | 80 | 2.84% | 79 | 2.8% |
Galea (2013) | 93 | 1.55% | 88 | 3.11% | 88 | 3.12% | 88 | 3.12% |
Grasshoff (2007) | 93 | 1.55% | 88 | 3.11% | 88 | 3.12% | 88 | 3.12% |
Fourt et al. (2017) | 82 | 1.37% | 78 | 2.76% | 78 | 2.77% | 78 | 2.77% |
Pichon (comm. pers., 2012) | 82 | 1.37% | 68 | 2.41% | 68 | 2.41% | 68 | 2.41% |
Diaz & Cuzange (2009) | 76 | 1.27% | 59 | 2.09% | 59 | 2.09% | 58 | 2.06% |
Gravier-Bonnet et al. (2007) | 74 | 1.23% | 57 | 2.02% | 57 | 2.02% | 57 | 2.02% |
Poupin et al. (1999) | 72 | 1.2% | 64 | 2.26% | 64 | 2.27% | 64 | 2.27% |
Uicn et al. (2020) | 66 | 1.1% | 59 | 2.09% | 59 | 2.09% | 59 | 2.09% |
Fautin (2013) | 58 | 0.97% | 53 | 1.88% | 52 | 1.85% | 52 | 1.85% |
Schleyer & Benayahu (2016) | 56 | 0.93% | 56 | 1.98% | 56 | 1.99% | 56 | 1.99% |
Dana (1846-1849) | 55 | 0.92% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Chevalier & Kuhlmann (1983) | 54 | 0.9% | 33 | 1.17% | 33 | 1.17% | 33 | 1.17% |
Galea & Schuchert (2019) | 53 | 0.88% | 52 | 1.84% | 52 | 1.85% | 52 | 1.85% |
Galea (2016) | 52 | 0.87% | 52 | 1.84% | 52 | 1.85% | 52 | 1.85% |
Godet et al. (2010) | 45 | 0.75% | 35 | 1.24% | 35 | 1.24% | 35 | 1.24% |
Galea (2010) | 44 | 0.73% | 37 | 1.31% | 37 | 1.31% | 37 | 1.31% |
Galea (2008) | 41 | 0.68% | 39 | 1.38% | 39 | 1.38% | 39 | 1.38% |
Fenner & Muir (2008) | 40 | 0.67% | 34 | 1.2% | 34 | 1.21% | 34 | 1.21% |
Martin (2011) | 39 | 0.65% | 31 | 1.1% | 31 | 1.1% | 31 | 1.1% |
Bedot (1910) | 38 | 0.63% | 20 | 0.71% | 20 | 0.71% | 20 | 0.71% |
Benayahu & van Ofwegen (2012) | 38 | 0.63% | 37 | 1.31% | 37 | 1.31% | 37 | 1.31% |
Duchassaing et al. (1860) | 38 | 0.63% | 14 | 0.5% | 14 | 0.5% | 13 | 0.46% |
Thélohan (1895) | 38 | 0.63% | 22 | 0.78% | 22 | 0.78% | 22 | 0.78% |
Arnaud (1974) | 34 | 0.57% | 13 | 0.46% | 13 | 0.46% | 13 | 0.46% |
Naumov & Stepanjants (1972) | 34 | 0.57% | 12 | 0.42% | 12 | 0.43% | 12 | 0.43% |
Reveillaud et al. (2008) | 34 | 0.57% | 32 | 1.13% | 32 | 1.14% | 31 | 1.1% |
Millard (1977) | 33 | 0.55% | 28 | 0.99% | 28 | 0.99% | 28 | 0.99% |
Orrell (2019) | 33 | 0.55% | 28 | 0.99% | 28 | 0.99% | 28 | 0.99% |
Pena et al. (2010) | 33 | 0.55% | 33 | 1.17% | 33 | 1.17% | 33 | 1.17% |
Gravier-Bonnet & Bourmaud (2005) | 30 | 0.5% | 24 | 0.85% | 24 | 0.85% | 24 | 0.85% |
Sheppard (1987) | 30 | 0.5% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Bigot (comm. pers., 2018) | 27 | 0.45% | 26 | 0.92% | 26 | 0.92% | 26 | 0.92% |
Breton (2014) | 27 | 0.45% | 22 | 0.78% | 22 | 0.78% | 22 | 0.78% |
Galea et al. (2021) | 27 | 0.45% | 27 | 0.96% | 27 | 0.96% | 27 | 0.96% |
Motz-Kossowska (1910) | 27 | 0.45% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Pax (1922) | 26 | 0.43% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
AAMP (2010) | 24 | 0.4% | 24 | 0.85% | 23 | 0.82% | 24 | 0.85% |
Duchassaing et al. (1864) | 24 | 0.4% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Linnaeus (1758) | 24 | 0.4% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
Mackay (2014) | 24 | 0.4% | 21 | 0.74% | 21 | 0.75% | 21 | 0.75% |
IUCN (2013) | 21 | 0.35% | 17 | 0.6% | 17 | 0.6% | 17 | 0.6% |
Lindner (2007) | 21 | 0.35% | 19 | 0.67% | 19 | 0.67% | 19 | 0.67% |
National Institute of Water and Atmospheric Research (2016) | 21 | 0.35% | 16 | 0.57% | 16 | 0.57% | 16 | 0.57% |
Peralta & Fautin (2013) | 20 | 0.33% | 10 | 0.35% | 9 | 0.32% | 10 | 0.35% |
Quelch (1886) | 20 | 0.33% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Vervoort & Vasseur (1977) | 20 | 0.33% | 12 | 0.42% | 12 | 0.43% | 12 | 0.43% |
Galea & Ferry (2015) | 19 | 0.32% | 17 | 0.6% | 17 | 0.6% | 17 | 0.6% |
Gardiner (1899) | 19 | 0.32% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Pearman et al. (2020) | 19 | 0.32% | 16 | 0.57% | 16 | 0.57% | 16 | 0.57% |
European Nucleotide Archive (2019) | 18 | 0.3% | 18 | 0.64% | 18 | 0.64% | 18 | 0.64% |
Flot & Adjeroud (2009) | 18 | 0.3% | 16 | 0.57% | 16 | 0.57% | 16 | 0.57% |
Galea (2015) | 18 | 0.3% | 18 | 0.64% | 18 | 0.64% | 18 | 0.64% |
Galea (2020) | 18 | 0.3% | 17 | 0.6% | 17 | 0.6% | 17 | 0.6% |
Bosserelle et al. (2014) | 17 | 0.28% | 16 | 0.57% | 16 | 0.57% | 16 | 0.57% |
Hourigan (2020) | 17 | 0.28% | 17 | 0.6% | 17 | 0.6% | 17 | 0.6% |
Rignault & Chevallier (2017) | 17 | 0.28% | 14 | 0.5% | 14 | 0.5% | 14 | 0.5% |
Postaire et al. (2016) | 16 | 0.27% | 13 | 0.46% | 13 | 0.46% | 13 | 0.46% |
Kitahara & Cairns (2009) | 15 | 0.25% | 15 | 0.53% | 15 | 0.53% | 15 | 0.53% |
Kitahara et al. (2010) | 15 | 0.25% | 15 | 0.53% | 15 | 0.53% | 15 | 0.53% |
Richer de Forges et al. (2005) | 15 | 0.25% | 14 | 0.5% | 14 | 0.5% | 14 | 0.5% |
Schleyer et al. (2016) | 15 | 0.25% | 14 | 0.5% | 14 | 0.5% | 14 | 0.5% |
Allman (1876) | 14 | 0.23% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Brugneaux & Pérès (2006) | 14 | 0.23% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Cairns (1986) | 14 | 0.23% | 14 | 0.5% | 14 | 0.5% | 14 | 0.5% |
D'hondt & D'hondt (2020) | 14 | 0.23% | 14 | 0.5% | 13 | 0.46% | 13 | 0.46% |
Moseley ([1880]) | 14 | 0.23% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
Bedot (1914) | 13 | 0.22% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Galea & Maggioni (2020) | 13 | 0.22% | 13 | 0.46% | 13 | 0.46% | 13 | 0.46% |
Gravier-Bonnet et al. (2022) | 13 | 0.22% | 12 | 0.42% | 12 | 0.43% | 12 | 0.43% |
Impact-Mer et al. (2011) | 13 | 0.22% | 10 | 0.35% | 10 | 0.35% | 10 | 0.35% |
Low & Evenhuis (2013) | 13 | 0.22% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Mémoires du Muséum National d'Histoire Naturelle, 8 (6) :225-248">Pax & Müller (1956) | 13 | 0.22% | 13 | 0.46% | 13 | 0.46% | 13 | 0.46% |
Totton (1930) | 13 | 0.22% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Agassiz & Mayer (1902) | 12 | 0.2% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cantero (2020) | 12 | 0.2% | 12 | 0.42% | 12 | 0.43% | 12 | 0.43% |
Fautin (2007) | 12 | 0.2% | 10 | 0.35% | 10 | 0.35% | 10 | 0.35% |
Goulletquer (2016) | 12 | 0.2% | 11 | 0.39% | 11 | 0.39% | 11 | 0.39% |
Gravier-Bonnet et al. (2009) | 12 | 0.2% | 11 | 0.39% | 11 | 0.39% | 11 | 0.39% |
Zibrowius (1968) | 12 | 0.2% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Anonyme (2023) | 11 | 0.18% | 11 | 0.39% | 11 | 0.39% | 11 | 0.39% |
Dai & Jeng (2016) | 11 | 0.18% | 10 | 0.35% | 10 | 0.35% | 10 | 0.35% |
Goud et al. (2021) | 11 | 0.18% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Mccrady (1859) | 11 | 0.18% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pourtalès (1880) | 11 | 0.18% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
. Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 11 | 0.18% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Ansín Agís et al. (2014) | 10 | 0.17% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
D'hondt & D'hondt (2018) | 10 | 0.17% | 10 | 0.35% | 8 | 0.28% | 10 | 0.35% |
Gravier-Bonnet & Bourmaud (2006) | 10 | 0.17% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Harvard University Museum & Morris P.J. (2020) | 10 | 0.17% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Payri et al. (2002) | 10 | 0.17% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
Verseveldt (1977) | 10 | 0.17% | 10 | 0.35% | 10 | 0.35% | 10 | 0.35% |
Allman (1888) | 9 | 0.15% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Ansín Agís et al. (2009) | 9 | 0.15% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
Ansín Agís et al. (2016) | 9 | 0.15% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Ifremer (2020) | 9 | 0.15% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Lamouroux (1816) | 9 | 0.15% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Le Sueur (1817) | 9 | 0.15% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Milne-Edwards (1848) | 9 | 0.15% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pourtales (1868) | 9 | 0.15% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Tixier-Durivault & Lafargue (1969) | 9 | 0.15% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Van Ofwegen (2002) | 9 | 0.15% | 9 | 0.32% | 9 | 0.32% | 9 | 0.32% |
Adjeroud et al. (2012) | 8 | 0.13% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Arrigoni et al. (2016) | 8 | 0.13% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Caziot (1921) | 8 | 0.13% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Collectif & Bebest (2019) | 8 | 0.13% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Deichmann (1936) | 8 | 0.13% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Duchassaing & Fonbressin (1870) | 8 | 0.13% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Galea et al. (2022) | 8 | 0.13% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Georgévitch (1916) | 8 | 0.13% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Ifremer (2022) | 8 | 0.13% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Bulletin de la Société Zoologique de France, 38: 282-288, 304-315.">Le Danois (1913) | 8 | 0.13% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pallas (1766) | 8 | 0.13% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Redier (1971) | 8 | 0.13% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Roule (1900) | 8 | 0.13% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Svoboda & Cornelius (1991) | 8 | 0.13% | 8 | 0.28% | 8 | 0.28% | 8 | 0.28% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 37: 1-243.">Bigelow (1909) | 7 | 0.12% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Billard (1923) | 7 | 0.12% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Cairns (2000) | 7 | 0.12% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
MGnify (2017) | 7 | 0.12% | 7 | 0.25% | 7 | 0.25% | 7 | 0.25% |
Alder (1859) | 6 | 0.1% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Cairns (1989) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Cairns (2004) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Chevaldonné et al. (2015) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 5 | 0.18% |
Dewarumez et al. (2011) | 6 | 0.1% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Dolan (2014) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Kitahara & Cairns (2008) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Linnaeus (1767) | 6 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Molodtsova (2007) | 6 | 0.1% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Nowaczyk et al. (2016) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Opresko (2004) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Pax & Müller (1956) | 6 | 0.1% | 4 | 0.14% | 1 | 0.04% | 4 | 0.14% |
Sartoretto (2012) | 6 | 0.1% | 6 | 0.21% | 6 | 0.21% | 6 | 0.21% |
Uicn et al. (2019) | 6 | 0.1% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Zibrowius (1974) | 6 | 0.1% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Bale (1888) | 5 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Billard (1919) | 5 | 0.08% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bouillon & Deroux (1967) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Duchassaing & Fontbressin (1850) | 5 | 0.08% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Ellis & Solander (1786) | 5 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hertwig (1882) | 5 | 0.08% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Jarms & Morandini (2019) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Lindner et al. (2014) | 5 | 0.08% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Montenegro et al. (2015) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 5 | 0.08% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Quod et al. (1995) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Sauvage (1886) | 5 | 0.08% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Schuchert (2008) | 5 | 0.08% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Schuchert (2017) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Sinniger (2007) | 5 | 0.08% | 5 | 0.18% | 5 | 0.18% | 5 | 0.18% |
Taylor & Rogers (2015) | 5 | 0.08% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Volpi & Benvenuti (2003) | 5 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells (1968) | 5 | 0.08% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Ambroso et al. (2013) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Arrigoni et al. (2018) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Arrigoni et al. (2020) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Australian Museum (2020) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Bayer & Stefani (1988) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bayer (1996) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Benzoni et al. (2010) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouillon (1965) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Carpine & Grasshoff (1975) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
DORIS (2012) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Duchassaing & Michelin (1846) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Fowler (1888) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea & Maggioni (2021) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Galea & Schories (2012) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Gall (2021) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Grasshoff (1996) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Lacassagne (1968) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Lutz & Ginsburg (2007) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Mao et al. (2020) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Migot & Portmann (1926) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Millard (1957) | 4 | 0.07% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Milne et al. (1857) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Olivier et al. (2015) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Quelch (1884) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Stiasny (1951) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Swain (2009) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Swedmark & Teissier (1957) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Thélohan (1892) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Thélohan (1892) | 4 | 0.07% | 4 | 0.14% | 4 | 0.14% | 4 | 0.14% |
Tur (1993) | 4 | 0.07% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Vaughan (1906) | 4 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bale (1924) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bayer (1990) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Bedot (1888) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Archives de zoologie expérimentale et générale, 57: 21-27.">Billard (1918) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Billard (1922) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Cairns (2016) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Carré (1968) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Carré (1968) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Carré (1969) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (1969) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Carricart-Ganivet & Reyes-Bonilla (1999) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cépède (1906) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Chevalier (1971) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Chintiroglu & Doumenc (1998) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Clarke (1879) | 3 | 0.05% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2008) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2014) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt & Tixier-Durivault (1975) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufaure (1959) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål (1775) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gadeau de Kerville (1900) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea et al. (2012) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Gardiner (1897) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Hiles (1899) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Hoffmeister (1929) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Irei et al. (2015) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Johnston & Burgess (2023) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Lamarck (1816) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lom et al. (1983) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Miranda et al. (2009) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Molodtsova (2007) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Moore et al. (2016) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Moser (1919) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Paulay & Brown (2019) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Péres (1925) | 3 | 0.05% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Pérez (1920) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1958) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Picard (1960) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Pyle et al. (2016) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Questel (2022) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Risso ([1827]) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ross & Zamponi (1983) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Swedmark & Teissier (1958) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Teissier (1922) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Telenius & Shah (2019) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Terrana et al. (2024) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Vanhöffen (1903) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Vaughan (1907) | 3 | 0.05% | 3 | 0.11% | 3 | 0.11% | 3 | 0.11% |
Mémoires de la Societé Zoologique de France, 12: 29-58.">Versluys (1899) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vervoort & Watson (2003) | 3 | 0.05% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Weill & Weill (1935) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 3 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1849) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Albertini-Berhaut (1970) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Albertini-berhaut (1970) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Tijdschrift der Nederlandse Dierkundige Vereeniging (Ser. 2), 7: 89-115.">Alcock (1902) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Alder (1856) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Ansin et al. (2004) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Aurivillius (1931) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bayer et al. (2016) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bayer (1959) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Benzoni & Pichon (2004) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Benzoni et al. (2014) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Benzoni (2013) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Berberian et al. (2021) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Proceedings of the United States National Museum, 44: 1-119.">Bigelow (1913) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bulletin de la Société zoologique de France, 45: 144-147.">Billard (1920) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bonnet et al. (2012) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Boschma (1964) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouillon & Gravier-Bonnet (1987) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Bourne (1890) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouxin & Prouzet (2021) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Brook (1892) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Buecher (1999) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cairns & Zibrowius (2016) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cairns (1977) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cairns (1979) | 2 | 0.03% | 2 | 0.07% | 1 | 0.04% | 2 | 0.07% |
Cairns (1995) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cairns (2010) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
, 22 (4): 1-144.">Calgren (1928) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cambert et al. (2011) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
Cantero (2022) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Carlgren (1918) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Cordeiro et al. (2018) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Curd et al. (2015) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Damas (1934) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Den Hartog (1987) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Den Hartog (1995) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Desportes & Theodorides (1983) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devictor & Morton (2010) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
D'hondt & D'hondt (2019) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
D'hondt (1986) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
D'hondt (1992) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
DORIS (2020) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Doumenc (1973) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eibye-jacobsen et al. (2019) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Esper ([1791]-1794) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Fautin (2009) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Forbes (1848) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser (1948) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea & Ferry (2013) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Galea et al. (2018) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Galea et al. (2020) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Galea (2021) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gardiner (1900) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Goy (1965) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Grasshoff & Bargibant (2001) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gravier (1913) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gray (1860) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Groot & Weinberg (1982) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Gutt et al. (2007) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Haeckel (1864) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Haeckel (1879) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1868) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hertwig (1888) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1855) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1861) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2021) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Jarms et al. (2003) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Jarvis (1922) | 2 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Léger (1930) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Léger (1931) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Licandro et al. (2004) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Lindström (1877) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linsley et al. (1999) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Macleod et al. (2024) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Maréchal & Trégarot (2012) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Mcfadden & Breton Hutchinson (2004) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
McFadden et al. (2024) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Mckenna et al. (2009) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Migot & Portmann (1926) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Modeer (1791) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Molodtsova (2005) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Monteiro et al. (1997) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moser et al. (1976) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Müller (1776) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Núñez et al. (2000) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Opresko (1996) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Opresko (2015) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pampoulie et al. (1999) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Pante & France (2010) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Peña Cantero & Vervoort (2003) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Prouzet et al. (2010) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Remane (1927) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Schuchert (2013) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Scorrano et al. (2016) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Sheppard et al. (2008) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Stechow (1923) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Straehler-pohl (2019) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Studer (1879) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor et al. (2013) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Teissier & Teissier (1925) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier-durivault (1964) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Turak et al. (2008) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Turak et al. (2014) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Umbgrove (1940) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Valkanov (1965) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Veron (2000) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Verseveldt (1976) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Weinberg (2013) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wells (1961) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1971) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1974) | 2 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wijsman-Best (1970) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wirtz & Diesel (1983) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wright & Studer (1889) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Wuennemann et al. (2016) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Yiu & Qiu (2022) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Zhan (2023) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Zibrowius (1980) | 2 | 0.03% | 2 | 0.07% | 2 | 0.07% | 2 | 0.07% |
Agassiz (1862) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Alder (1857) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Allman (1859) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Allspach & Carsten (2020) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Allspach & Janussen (2020) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Altuna et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Altuna Prados & Álvarez Claudio (1994) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Améziane et al. (2011) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
André (2009) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Andres (1883) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ansin Agis et al. (2001) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Aronson et al. (2008) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aronson et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Arrigoni et al. (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Arvy (1972) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Auby (1993) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Balvay (2009) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bayer et al. (2013) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Beauchamp (1914) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Benajiba et al. (1995) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bernard (1896) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bernard (1897) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bernard (1897) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bigelow (1909) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bigot et al. (2006) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bigot (2006) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Boissin et al. (2019) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Borojevic (1971) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon & Bouchon (1999) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourdillon (1955) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Bourne (1916) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Brook (1891) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cairns (1979) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cairns (1998) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cairns (2012) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Canese & Bavestrello (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Canning et al. (1999) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carlgren (1924) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Carlgren (1928) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Carlgren (1943) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Carter (1995) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Casamajor de et al. (2023) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Casamajor et al. (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Casamajor et al. (2021) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Casamajor et al. (2022) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cauvin (2010) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cecchini (1914) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cerfontaine (1891) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chintiroglou & Stephanidou (1996) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Chun (1896) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocks (1854) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppari et al. (2020) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cuif et al. (2003) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Cunningham (1892) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Davoult et al. (1993) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Delle Chiaje (1841-1844) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dennant (1904) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2008) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
deVantier et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
deVantier et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Devantier et al. (2014) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
deVantier et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
deVantier et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
deVantier et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
deVantier et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
D'hondt & D'hondt (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Duncan (1865) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duncan (1876) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Duncan (1889) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eglot et al. (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Ekström (2021) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Eschscholtz (1829) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Faure (1982) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Ferreira & Gonçalves (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Fewkes (1881) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Forbes (1843) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1957) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål & Niebuhr (1775) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fortic et al. (2023) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Forum DORIS (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Galea & Maggioni (2024) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Galea (2007) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gardiner (1898) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gegenbaur et al. (1853) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gegenbaur (1857) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Glémarec et al. (1987) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
González-Muñoz et al. (2013) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gravier (1910) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gravier (1922) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Gregory (1895) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gu et al. (2022) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Haddon & Shackleton (1893) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Haeckel (1880) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harmelin & Garrabou (2005) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hartlaub (1901) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hartmann-Schröder (1985) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Head (1978) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Henderson & Okamura (2004) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hincks (1861) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoeksema & Vicente (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hoeksema et al. (2014) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoeksema et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hoeksema et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hoeksema et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hoeksema et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hoeksema (2012) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Hughes (1983) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
ICZN (2011) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Johnson (1861) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1847) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Julien (1881) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayal & Kayal (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Kitahara (2005) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Klunzinger (1879) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kölliker (1853) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Korzhavina & Ivanenko (2019) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Kousteni et al. (2019) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Krohn (1853) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2009) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Kükenthal (1907) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kweitniewski (1898) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacaze-Duthiers (1897) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Lamouroux (1821) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lankester (1880) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Laval (1968) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Travaux du Laboratoire d'Hydrobiologie Grenoble, 21: 7-14.">Léger (1930) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Leloup (1935) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lima et al. (2019) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeuillet et al. (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Maas (1903) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
MacGillivray (1842) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mackay & Rowden (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Manjarrés (1978) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Marchessaux et al. (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Marion (1878) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mayer (1910) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Mckenna et al. (2006) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Mckenna et al. (2011) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Michez et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Millard & Bouillon (1975) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Mills et al. (2018) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne & Edwards (1860) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne et al. (1857) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Molinari et al. (2023) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Molnar et al. (2008) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Molodtsova (2016) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moseley (1879) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Moura et al. (2012) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Nemenzo (1976) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Noël, Chevallier (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Noël (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Noël (2017) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Nolf & Cahuzac (2009) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Norman (1867) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Nutting (1905) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Obura et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Ocana & Brito (2004) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ott (1995) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Otto (1823) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Owens (1994) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Pampoulie & Morand (2002) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Panceri (1869) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Payri et al. (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Pennant (1777) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1920) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Philippi (1835) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1951) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pichon et al. (2020) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Pictet (1893) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Zoologischer Anzeiger, 7: 148-152, 164-169, 185-188, 216-221.">Pieper (1884) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pourtalès (1874) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Prouzet & Ziemski (2021) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Prouzet et al. (2010) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Prouzet (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
. Paris: 390 pp.">Quoy & Gaimard (1832-1835) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Rapp (1828) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rees & White (1957) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Renaud-Mornant & Jouin (1965) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Richards et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Richards et al. (2014) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Richer de Forges & Pianet (1984) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Risso (1826) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Roth (1871) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Rudi et al. (1998) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Saemundsson (1911) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Samyn & Vandenberghe (2021) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1835) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Sars (1857) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1874) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Schleyer (2013) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Schuchert & Collins (2021) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Schuchert (2000) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchert (2008) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sentz-Braconnot & Carré (1966) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Sheppard et al. (2008) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sheppard et al. (2014) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1941) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Stampar et al. (2020) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Stechow (1923) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Stechow (1932) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
36-40.">Stephenson (1918) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stock (1986) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Thomson et al. (1909) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Torelli (1961) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Torres-Pratts et al. (2011) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Trebilcock (1928) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Turak et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Vaga et al. (2023) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Valenciennes (1846) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Van et al. (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Veron & Wallace (1984) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Veron et al. (1977) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Veron (1985) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Veron (1985) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Verrill (1864) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Verrill (1864) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Verrill (1872) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Verrill (1901) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallace & Wolstenholme (1998) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Wallace (1994) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Wallace (1999) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Watson (2003) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Watson (2008) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Weinberg (1978) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2016) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Yabe & Sugiyama (1937) | 1 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
Zibrowius & Arnaud (1995) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zibrowius (1982) | 1 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |