Décapodes de Martinique
211 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Poupin & Corbari (2016) | 119 | 14,93% | 102 | 31,58% | 102 | 31,58% | 102 | 31,58% |
| Poupin (2018) | 76 | 9,54% | 65 | 20,12% | 65 | 20,12% | 65 | 20,12% |
| Carmona-Suárez & Poupin (2016) | 75 | 9,41% | 58 | 17,96% | 58 | 17,96% | 58 | 17,96% |
| Questel (2020) | 72 | 9,03% | 71 | 21,98% | 71 | 21,98% | 71 | 21,98% |
| Carré (2006) | 67 | 8,41% | 53 | 16,41% | 53 | 16,41% | 53 | 16,41% |
| Tricart & Foubert (2000) | 58 | 7,28% | 43 | 13,31% | 43 | 13,31% | 43 | 13,31% |
| Poupin (2010) | 49 | 6,15% | 48 | 14,86% | 48 | 14,86% | 48 | 14,86% |
| Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 48 | 6,02% | 8 | 2,48% | 8 | 2,48% | 8 | 2,48% |
| Paulmier (1996) | 45 | 5,65% | 32 | 9,91% | 32 | 9,91% | 32 | 9,91% |
| Poupin (1994) | 45 | 5,65% | 35 | 10,84% | 35 | 10,84% | 35 | 10,84% |
| Corbari et al. (2020) | 42 | 5,27% | 39 | 12,07% | 39 | 12,07% | 39 | 12,07% |
| Questel & Le Quellec (2012) | 30 | 3,76% | 25 | 7,74% | 25 | 7,74% | 25 | 7,74% |
| Corbari et al. (2015) | 27 | 3,39% | 22 | 6,81% | 22 | 6,81% | 22 | 6,81% |
| Ashrafi & Hultgren (2022) | 21 | 2,63% | 21 | 6,5% | 21 | 6,5% | 21 | 6,5% |
| Poupin & Lemaitre (2014) | 17 | 2,13% | 17 | 5,26% | 17 | 5,26% | 17 | 5,26% |
| Lim et al. (2002) | 13 | 1,63% | 13 | 4,02% | 13 | 4,02% | 13 | 4,02% |
| Monti et al. (2010) | 13 | 1,63% | 13 | 4,02% | 13 | 4,02% | 13 | 4,02% |
| UICN Comité français, OFB & MNHN (2021) | 13 | 1,63% | 13 | 4,02% | 13 | 4,02% | 13 | 4,02% |
| Guéguen (2000) | 10 | 1,25% | 7 | 2,17% | 7 | 2,17% | 7 | 2,17% |
| Machordom et al. (2022) | 8 | 1% | 8 | 2,48% | 8 | 2,48% | 8 | 2,48% |
| Yokoyama (2013) | 7 | 0,88% | 6 | 1,86% | 6 | 1,86% | 6 | 1,86% |
| Farfante (1971) | 6 | 0,75% | 6 | 1,86% | 6 | 1,86% | 6 | 1,86% |
| Saussure (1857) | 6 | 0,75% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anker & Baeza (2021) | 5 | 0,63% | 5 | 1,55% | 5 | 1,55% | 5 | 1,55% |
| Beltran (1982) | 5 | 0,63% | 5 | 1,55% | 5 | 1,55% | 5 | 1,55% |
| Coutiere (1909) | 5 | 0,63% | 5 | 1,55% | 5 | 1,55% | 5 | 1,55% |
| Crosnier (1976) | 5 | 0,63% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Questel (2014) | 5 | 0,63% | 5 | 1,55% | 5 | 1,55% | 5 | 1,55% |
| Rodriguez et al. (2019) | 5 | 0,63% | 3 | 0,93% | 3 | 0,93% | 3 | 0,93% |
| Uicn et al. (2019) | 5 | 0,63% | 5 | 1,55% | 5 | 1,55% | 5 | 1,55% |
| Anker et al. (2012) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Fourt et al. (2017) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Guinot et al. (2018) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Holthuis (1951) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Ifremer (2009) | 4 | 0,5% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Pinheiro & Boos (2016) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Questel (2017) | 4 | 0,5% | 4 | 1,24% | 4 | 1,24% | 4 | 1,24% |
| Stimpson (1871) | 4 | 0,5% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Diaz & Cuzange (2009) | 3 | 0,38% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Goulletquer (2016) | 3 | 0,38% | 3 | 0,93% | 3 | 0,93% | 3 | 0,93% |
| Linnaeus (1758) | 3 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin et al. (1999) | 3 | 0,38% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Poupin et al. (2013) | 3 | 0,38% | 3 | 0,93% | 3 | 0,93% | 3 | 0,93% |
| Schmitt (1933) | 3 | 0,38% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Anker (2007) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Baba & Wicksten (2017) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Baudry et al. (2022) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Bell (1836) | 2 | 0,25% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Brandao et al. (2010) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Burkenroad (1939) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Chace (1972) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Chen et al. (2016) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Churchill (1942) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Farfante (1967) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garcia (1977) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Hines et al. (1995) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Holthuis (1958) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Hultgren et al. (2010) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| IUCN (2013) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Lucas (1846) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macia & Robinson (2009) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Mclaughlin (1981) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Milne-edwards (1837) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nguyen & Ngoc-Ho (1989) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Nobili (1906) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliveira et al. (2016) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Oliviera (1939) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patton et al. (1985) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Rathbun (1918) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1816) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robles et al. (2007) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Rojas-Beltran (1981) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Sarver et al. (1998) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1936) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shirley & Wolcott (1991) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Stebbing (1917) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1871) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals & Magazine of Natural History Series 9, 6: 220-226.">Sund (1920) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tollu (2009) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Turkay (1975) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Wass (1963) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williamson et al. (2012) | 2 | 0,25% | 2 | 0,62% | 2 | 0,62% | 2 | 0,62% |
| Abbe (1974) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Amanieu & Dantec (1961) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Anker & Tóth (2008) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Anker (2012) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Anker (2012) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Anonyme (2008) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Ary et al. (1985) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Barnard (1950) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bauer (1985) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Boone (1927) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouvier (1901) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Comptes rendus hebdomadaires des séances de l'Académie des sciences, 141: 746-749.">Bouvier (1905) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (2014) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Bruce (1974) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Brumbaugh & Mcconaugha (1995) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Cardoso & Young (2007) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Chace (1939) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Chace (1962) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Chan (1991) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevaldonne et al. (2023) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Coelho (1972) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costlow et al. (1958) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Costlow (1967) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Cronin (1949) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Crosnier (1986) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Curd et al. (2015) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Daugherty (1952) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Davis et al. (2004) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Dewarumez et al. (2011) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Dittel et al. (2006) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Duffy (1996) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Fabricius (1793) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferry et al. (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Fingerman (1955) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Forest & Saint Laurent | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Forward et al. (2003) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Freeman et al. (1987) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Galil et al. (2016) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Galil (2000) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Gall & Beague (1986) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Garth (1951) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Gomez (1933) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gonzalez-ortegon et al. (2020) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Goud et al. (2021) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Goy (2015) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Gray & Newcombe (1938) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Guinot-dumortier (1960) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Gunter (1938) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Havens et al. (2009) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Hay (1917) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heard (1986) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Holthuis (1950) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Holthuis (1951) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1977) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Huff (1979) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Impact-Mer et al. (2011) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Ives (1891) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan & Mille (2006) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Jourdan (2020) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Jourde et al. (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Keith et al. (2002) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Keith et al. (1999) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Kingsley (1878) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Labrune et al. (2019) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lagarde (2008) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lalubie et al. (2015) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lebour (1949) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lemaitre (1996) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lenz & Strunck (1914) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Li (2008) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lochhead & Newcombe (1942) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Lockington (1877) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macia & Robinson (2012) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Mancinelli et al. (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Mancinelli et al. (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Manning & Chace (1990) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Manning & Holthuis (1989) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Manning (1988) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Milne-edwards & Bouvier (1897) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne-edwards (1873-1880) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Milne-Edwards (1878) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Mulochau et al. (2019) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Murienne et al. (2022) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Nelson-Smith et al. (2014) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Newcombe et al. (1949) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Nobili (1905) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël & Boulad (2018) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Noël & Prouzet (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Noël (2015) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Noël (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Noël (2017) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Olivier (1791-[1792]) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pêpe et al. (2021) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Pezy et al. (2019) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Poupin et al. (2018) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Rathbun (1892) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rathbun (1896) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Rathbun (1898) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Rathbun (1901) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Rathbun (1920) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rhyne & Lin (2006) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Rios & Duffy (2007) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ríos & Duffy (2007) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roudez et al. (2008) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Ryer et al. (1997) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Sadek et al. (2018) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Sanchez (1977) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sandoz & Rogers (1944) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Saussure (1853) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1924) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Schmitt (1939) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Singh (2021) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Snijders & Fransen (2010) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Stimpson (1860) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Stimpson (1860) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Tavares & Amouroux (2003) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Thongda et al. (2015) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Torres et al. (2006) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Vereshchaka et al. (2020) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vincent (1986) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Weckel (2019) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Weissburg & Zimmer-faust (1994) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
| Wolcott et al. (2005) | 1 | 0,13% | 1 | 0,31% | 1 | 0,31% | 1 | 0,31% |
