Hydrozoaires
Hydrozoa
250 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Cairns (2015) | 162 | 7,13% | 158 | 16,67% | 158 | 16,67% | 158 | 16,67% |
Ifremer (2009) | 102 | 4,49% | 94 | 9,92% | 94 | 9,92% | 94 | 9,92% |
Gravier-Bonnet (2007) | 101 | 4,45% | 86 | 9,07% | 86 | 9,07% | 86 | 9,07% |
Vervoort (1993) | 98 | 4,31% | 87 | 9,18% | 87 | 9,18% | 87 | 9,18% |
Galea (2013) | 93 | 4,09% | 88 | 9,28% | 88 | 9,28% | 88 | 9,28% |
Gravier-Bonnet et al. (2007) | 74 | 3,26% | 57 | 6,01% | 57 | 6,01% | 57 | 6,01% |
Poupin et al. (1999) | 60 | 2,64% | 52 | 5,49% | 52 | 5,49% | 52 | 5,49% |
Galea & Schuchert (2019) | 53 | 2,33% | 52 | 5,49% | 52 | 5,49% | 52 | 5,49% |
Galea (2016) | 52 | 2,29% | 52 | 5,49% | 52 | 5,49% | 52 | 5,49% |
Bourmaud (2003) | 51 | 2,24% | 38 | 4,01% | 38 | 4,01% | 38 | 4,01% |
Galea (2010) | 44 | 1,94% | 37 | 3,9% | 37 | 3,9% | 37 | 3,9% |
Nelson-Smith et al. (2014) | 42 | 1,85% | 34 | 3,59% | 34 | 3,59% | 34 | 3,59% |
Galea (2008) | 41 | 1,8% | 39 | 4,11% | 39 | 4,11% | 39 | 4,11% |
Bedot (1910) | 38 | 1,67% | 20 | 2,11% | 20 | 2,11% | 20 | 2,11% |
Naumov & Stepanjants (1972) | 34 | 1,5% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Arnaud (1974) | 33 | 1,45% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Millard (1977) | 33 | 1,45% | 28 | 2,95% | 28 | 2,95% | 28 | 2,95% |
Pena et al. (2010) | 33 | 1,45% | 33 | 3,48% | 33 | 3,48% | 33 | 3,48% |
Gravier-Bonnet & Bourmaud (2005) | 30 | 1,32% | 24 | 2,53% | 24 | 2,53% | 24 | 2,53% |
Galea et al. (2021) | 27 | 1,19% | 27 | 2,85% | 27 | 2,85% | 27 | 2,85% |
Motz-Kossowska (1910) | 27 | 1,19% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Mackay (2014) | 24 | 1,06% | 21 | 2,22% | 21 | 2,22% | 21 | 2,22% |
Lindner (2007) | 21 | 0,92% | 19 | 2% | 19 | 2% | 19 | 2% |
Vervoort & Vasseur (1977) | 20 | 0,88% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Galea & Ferry (2015) | 19 | 0,84% | 17 | 1,79% | 17 | 1,79% | 17 | 1,79% |
Galea (2015) | 18 | 0,79% | 18 | 1,9% | 18 | 1,9% | 18 | 1,9% |
Galea (2020) | 18 | 0,79% | 17 | 1,79% | 17 | 1,79% | 17 | 1,79% |
Postaire et al. (2016) | 16 | 0,7% | 13 | 1,37% | 13 | 1,37% | 13 | 1,37% |
Linnaeus (1758) | 15 | 0,66% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Rignault & Chevallier (2017) | 15 | 0,66% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Allman (1876) | 14 | 0,62% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Cairns (1986) | 14 | 0,62% | 14 | 1,48% | 14 | 1,48% | 14 | 1,48% |
Godet et al. (2010) | 14 | 0,62% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Bedot (1914) | 13 | 0,57% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Breton (2014) | 13 | 0,57% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Galea & Maggioni (2020) | 13 | 0,57% | 13 | 1,37% | 13 | 1,37% | 13 | 1,37% |
Gravier-Bonnet et al. (2022) | 13 | 0,57% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Totton (1930) | 13 | 0,57% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Cantero (2020) | 12 | 0,53% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Gravier-Bonnet et al. (2009) | 12 | 0,53% | 11 | 1,16% | 11 | 1,16% | 11 | 1,16% |
Mccrady (1859) | 11 | 0,48% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Questel & Le Quellec (2012) | 11 | 0,48% | 10 | 1,05% | 10 | 1,05% | 10 | 1,05% |
Ansín Agís et al. (2014) | 10 | 0,44% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Gravier-Bonnet & Bourmaud (2006) | 10 | 0,44% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Questel (2020) | 10 | 0,44% | 10 | 1,05% | 10 | 1,05% | 10 | 1,05% |
AAMP (2010) | 9 | 0,4% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Allman (1888) | 9 | 0,4% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Ansín Agís et al. (2009) | 9 | 0,4% | 7 | 0,74% | 7 | 0,74% | 7 | 0,74% |
Ansín Agís et al. (2016) | 9 | 0,4% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Goulletquer (2016) | 9 | 0,4% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Agassiz & Mayer (1902) | 8 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Duchassaing et al. (1864) | 8 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
European Nucleotide Archive (2019) | 8 | 0,35% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Galea et al. (2022) | 8 | 0,35% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Lamouroux (1816) | 8 | 0,35% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Bulletin de la Société Zoologique de France, 38: 282-288, 304-315.">Le Danois (1913) | 8 | 0,35% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Redier (1971) | 8 | 0,35% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Svoboda & Cornelius (1991) | 8 | 0,35% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Tricart & Foubert (2000) | 8 | 0,35% | 8 | 0,84% | 8 | 0,84% | 8 | 0,84% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 37: 1-243.">Bigelow (1909) | 7 | 0,31% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Billard (1923) | 7 | 0,31% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Caziot (1921) | 7 | 0,31% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Alder (1859) | 6 | 0,26% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Andouche et al. (2020) | 6 | 0,26% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Dolan (2014) | 6 | 0,26% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Nowaczyk et al. (2016) | 6 | 0,26% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Orrell (2019) | 6 | 0,26% | 6 | 0,63% | 6 | 0,63% | 6 | 0,63% |
Bale (1888) | 5 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Billard (1919) | 5 | 0,22% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Bouillon & Deroux (1967) | 5 | 0,22% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Dana (1846-1849) | 5 | 0,22% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Diaz & Cuzange (2009) | 5 | 0,22% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Lindner et al. (2014) | 5 | 0,22% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Sauvage (1886) | 5 | 0,22% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Schuchert (2008) | 5 | 0,22% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Schuchert (2017) | 5 | 0,22% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Bouillon (1965) | 4 | 0,18% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Dewarumez et al. (2011) | 4 | 0,18% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Galea & Maggioni (2021) | 4 | 0,18% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Galea & Schories (2012) | 4 | 0,18% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Lacassagne (1968) | 4 | 0,18% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Millard (1957) | 4 | 0,18% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Olivier et al. (2015) | 4 | 0,18% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Swedmark & Teissier (1957) | 4 | 0,18% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Bale (1924) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bedot (1888) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Archives de zoologie expérimentale et générale, 57: 21-27.">Billard (1918) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Billard (1922) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (1968) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Carré (1968) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Carré (1969) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (1969) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Clarke (1879) | 3 | 0,13% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fenner & Muir (2008) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Forsskål (1775) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Gadeau de Kerville (1900) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea et al. (2012) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Harvard University Museum & Morris P.J. (2020) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Ifremer (2020) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Ifremer (2022) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lamarck (1816) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
MGnify (2017) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Pallas (1766) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Péres (1925) | 3 | 0,13% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pérez (1920) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1958) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Picard (1960) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Swedmark & Teissier (1958) | 3 | 0,13% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Teissier (1922) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mémoires de la Societé Zoologique de France, 12: 29-58.">Versluys (1899) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Vervoort & Watson (2003) | 3 | 0,13% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Weill & Weill (1935) | 3 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1849) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Albertini-Berhaut (1970) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Albertini-berhaut (1970) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Alder (1856) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Ansin et al. (2004) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Berberian et al. (2021) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Proceedings of the United States National Museum, 44: 1-119.">Bigelow (1913) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Bulletin de la Société zoologique de France, 45: 144-147.">Billard (1920) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Boschma (1964) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouillon & Gravier-Bonnet (1987) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Bourne (1890) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Buecher (1999) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Cantero (2022) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Chevalier & Kuhlmann (1983) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Curd et al. (2015) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Damas (1934) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Duchassaing & Michelin (1846) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Eibye-jacobsen et al. (2019) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Ellis & Solander (1786) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Forbes (1848) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Fraser (1948) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea & Ferry (2013) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Galea et al. (2018) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Galea et al. (2020) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Galea (2021) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Goy (1965) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Gray (1860) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Haeckel (1864) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Haeckel (1879) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1868) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1855) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1861) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Jarvis (1922) | 2 | 0,09% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Licandro et al. (2004) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mao et al. (2020) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Modeer (1791) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Peña Cantero & Vervoort (2003) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Remane (1927) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Schuchert (2013) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Stechow (1923) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Telenius & Shah (2019) | 2 | 0,09% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Valkanov (1965) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Vanhöffen (1903) | 2 | 0,09% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Agassiz (1862) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alder (1857) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Allman (1859) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Allspach & Carsten (2020) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Altuna Prados & Álvarez Claudio (1994) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ansin Agis et al. (2001) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Arvy (1972) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Australian Museum (2020) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Balvay (2009) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bigelow (1909) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boissin et al. (2019) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Borojevic (1971) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2010) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cocks (1854) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cunningham (1892) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Deuss et al. (2013) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Eschscholtz (1829) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fewkes (1881) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Flot & Adjeroud (2009) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forsskål & Niebuhr (1775) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea & Maggioni (2024) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Galea (2007) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gegenbaur (1857) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gmelin (1791) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goud et al. (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gu et al. (2022) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gutt et al. (2007) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hartlaub (1901) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hincks (1861) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hourigan (2020) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hughes (1983) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-Mer et al. (2011) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayal & Kayal (2017) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kölliker (1853) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kousteni et al. (2019) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Krohn (1853) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamouroux (1821) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lankester (1880) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Laval (1968) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Leloup (1935) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeuillet et al. (2017) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
MacGillivray (1842) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchessaux et al. (2017) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mayer (1910) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Millard & Bouillon (1975) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Molnar et al. (2008) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Moseley (1879) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moura et al. (2012) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Müller (1776) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
National Institute of Water and Atmospheric Research (2016) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël, Chevallier (2016) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Norman (1867) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Nutting (1905) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Otto (1823) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulay & Brown (2019) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pearman et al. (2020) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Peralta & Fautin (2013) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1951) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pictet (1893) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zoologischer Anzeiger, 7: 148-152, 164-169, 185-188, 216-221.">Pieper (1884) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pourtales (1868) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel (2022) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rees & White (1957) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Renaud-Mornant & Jouin (1965) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Richer de Forges et al. (2005) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roth (1871) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Saemundsson (1911) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Samyn & Vandenberghe (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1835) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sars (1857) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1874) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schuchert & Collins (2021) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schuchert (2000) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchert (2008) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sentz-Braconnot & Carré (1966) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sowerby (1941) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Stechow (1923) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Stechow (1932) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Trebilcock (1928) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (2003) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Watson (2008) | 1 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zilli (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |