Poissons d'eau douce de Guyane
Poissons d'eau douce (sens large) de Guyane : inclut les espèces strictement d'eau douce (habitat 2) ou également retrouvées dans le milieu marin (habitat 4 = eau douce / marin).
196 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Le Bail et al. (2012) | 373 | 23,58% | 351 | 71,49% | 351 | 72,07% | 349 | 71,52% |
| Sidlauskas & Vari (2012) | 24 | 1,52% | 24 | 4,89% | 24 | 4,93% | 24 | 4,92% |
| Uicn et al. (2017) | 24 | 1,52% | 23 | 4,68% | 23 | 4,72% | 23 | 4,71% |
| Eigenmann (1912) | 19 | 1,2% | 11 | 2,24% | 11 | 2,26% | 11 | 2,25% |
| Questel (2020) | 17 | 1,07% | 17 | 3,46% | 17 | 3,49% | 17 | 3,48% |
| Questel & Le Quellec (2012) | 15 | 0,95% | 15 | 3,05% | 15 | 3,08% | 15 | 3,07% |
| Covain et al. (2012) | 12 | 0,76% | 12 | 2,44% | 12 | 2,46% | 12 | 2,46% |
| Marceniuk & Menezes (2007) | 12 | 0,76% | 11 | 2,24% | 11 | 2,26% | 11 | 2,25% |
| Brosse et al. (2021) | 11 | 0,7% | 11 | 2,24% | 11 | 2,26% | 11 | 2,25% |
| Géry et al. (1991) | 10 | 0,63% | 8 | 1,63% | 8 | 1,64% | 8 | 1,64% |
| Louis et al. (1992) | 10 | 0,63% | 7 | 1,43% | 7 | 1,44% | 7 | 1,43% |
| Reis et al. (2003) | 10 | 0,63% | 10 | 2,04% | 10 | 2,05% | 10 | 2,05% |
| Smith (1997) | 10 | 0,63% | 6 | 1,22% | 4 | 0,82% | 6 | 1,23% |
| Lim et al. (2002) | 9 | 0,57% | 8 | 1,63% | 8 | 1,64% | 8 | 1,64% |
| Bouchon-Navaro et al. (2005) | 8 | 0,51% | 8 | 1,63% | 8 | 1,64% | 8 | 1,64% |
| Costa (2011) | 8 | 0,51% | 8 | 1,63% | 8 | 1,64% | 8 | 1,64% |
| Fisch-Muller et al. (2012) | 8 | 0,51% | 6 | 1,22% | 6 | 1,23% | 6 | 1,23% |
| Gery et al. (1996) | 8 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monti et al. (2010) | 8 | 0,51% | 8 | 1,63% | 8 | 1,64% | 8 | 1,64% |
| Huber (1991) | 7 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soubeyran (2008) | 7 | 0,44% | 7 | 1,43% | 7 | 1,44% | 7 | 1,43% |
| Duméril (1870) | 6 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fricke et al. (2009) | 6 | 0,38% | 5 | 1,02% | 5 | 1,03% | 5 | 1,02% |
| Pellegrin (1903) | 6 | 0,38% | 6 | 1,22% | 6 | 1,23% | 6 | 1,23% |
| Boeseman (1971) | 5 | 0,32% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Bouchon-Navaro & Louis (1986) | 5 | 0,32% | 5 | 1,02% | 5 | 1,03% | 5 | 1,02% |
| Keith et al. (2002) | 5 | 0,32% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Keith et al. (2013) | 5 | 0,32% | 5 | 1,02% | 5 | 1,03% | 5 | 1,02% |
| Bouchon-Navaro et al. (1992) | 4 | 0,25% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Covain & Fisch-Muller (2012) | 4 | 0,25% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Eigenmann (1908) | 4 | 0,25% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Fricke et al. (2011) | 4 | 0,25% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Heitmans et al. (1983) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2006) | 4 | 0,25% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Latham (1794) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucena & Malabarba (2010) | 4 | 0,25% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Mattox et al. (2006) | 4 | 0,25% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Pinna & Keith (2019) | 4 | 0,25% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Ponton & Merigoux (2000) | 4 | 0,25% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
| Puyo (1948) | 4 | 0,25% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Vaillant (1899) | 4 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béarez et al. (2017) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Betancur-r et al. (2008) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boeseman (1982) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Brugneaux & Pérès (2006) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Diaz & Cuzange (2009) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Duméril (1865) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faria et al. (2013) | 3 | 0,19% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Firmat et al. (2012) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Géry et al. (1988) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Géry et al. (1995) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Géry (1959) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Keith et al. (2006) | 3 | 0,19% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Keith (2002) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Kottelat ( 2013) | 3 | 0,19% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Lopez-fernandez & Winemiller (2003) | 3 | 0,19% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Nijssen & Isbrucker (1983) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Rapp et al. (2001) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Séret (1997) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Siu et al. (2017) | 3 | 0,19% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Toledo-piza & Menezes (1996) | 3 | 0,19% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| UICN Comité français, OFB & MNHN (2021) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Westby (1988) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Zarske et al. (2004) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarske et al. (2006) | 3 | 0,19% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
| Andrade et al. (2018) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Bacchet et al. (2007) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Berry & Smith-Vaniz (1978) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Bloch & Schneider (1801) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Compagno (1984) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Cuvier & Valenciennes (1846) | 2 | 0,13% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| de Morais et al. (2024) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| de Santana & Vari (2010) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Deynat (2006) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Fernandez-Carvalho et al. (2013) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Fischer (1884) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garcia-ayala et al. (2024) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Gargominy et al. (1996) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Gery & Planquette (1983) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Gery et al. (1998) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Gery (1992) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Harrison et al. (2007) | 2 | 0,13% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Hopkins (1991) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Isbrucker & Nijssen (1984) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Jégu et al. (2003) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Keith & Meunier (2000) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Keith et al. (1999) | 2 | 0,13% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Kullander (1982) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Kullander (2012) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Lowe et al. (2007) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Lujan et al. (2017) | 2 | 0,13% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Marquet et al. (2003) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Meunier et al. (2011) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Meunier et al. (2014) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Muller & Isbrucker (1993) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Myers (1960) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Nijssen & Isbrucker (1980) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Nijssen & Isbrucker (1990) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Parisi & Lundberg (2009) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Pascal et al. (1994) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Pellegrin (1902) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1908) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinna & Keith (2003) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Planquette et al. (1996) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousseau (2010) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Schomburgk (1841) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tavera et al. (2018) | 2 | 0,13% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| UICN France & MNHN (2013) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Uicn et al. (2020) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Vari et al. (2003) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vari et al. (2012) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Vari (1991) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitehead et al. (1988) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Yokoyama (2013) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Zarske et al. (2010) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Zarske (2012) | 2 | 0,13% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
| Alley et al. (2023) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Andrade et al. (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bail (2009) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Bleeker (1865) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon & Lemoine (2003) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Boujard et al. (1988) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boujard (1992) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Chabanaud (1927) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Chassaing et al. (2018) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Records of the Indian Museum (Calcutta). 2(4): 391-392.">Chaudhuri (1908) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conway et al. (2017) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Cope (1870) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Craig et al. (2017) | 1 | 0,06% | 1 | 0,2% | 0 | 0% | 1 | 0,2% |
| Crampton & Albert (2003) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Desse-berset & Williot (2011) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Desse-Berset & Williot (2012) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Desse-Berset (2012) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Fernandes et al. (2005) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Fraser-brunner (1947) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Gery (1961) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Gill (1858) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gory (1972) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Gozlan et al. (2010) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Grenand et al. (2015) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Günther (1864) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hein et al. (2010) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Hoedeman (1961) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jamonneau et al. (2025) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Jégu (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jegu et al. (2004) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Jégu (1998) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Jégu (2000) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Jordan (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourde et al. (2017) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Kaup (1856) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith & Dorson (2003) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Keith & Marquet (2011) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Keith et al. (2000) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2011) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Keith (2000) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Krøyer (1852-53) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lehmann et al. (2014) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Linnaeus (1758) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lundberg et al. (2012) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Lütken (1875) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marceniuk et al. (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Pérès (2007) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Maréchal & Trégarot (2012) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Matsuzaki et al. (2009) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Merckx et al. (2000) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Mitchill (1815) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Mol et al. (2012) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Moreira & Lima (2011) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Müller & Troschel (1844) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1929) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pascal et al. (2006) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Pellegrin (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1927) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Pieters & Dickinson (2005) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1858-61) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quéro & Delmas (1982) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2014) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Rafinesque (1820) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Regan (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reis et al. (2005) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santana et al. (2019) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Schindler (1998) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Silva et al. (2016) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Silva-Oliveira et al. (2020) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Silva-oliveira et al. (2021) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Simian et al. (2022) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
| Van der Stigchel (1947) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarske et al. (2006) | 1 | 0,06% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
