Invertébrés d'eau douce introduits en métropole
Tous les animaux non vertébrés affiliés au milieu aquatique (habitats 2, 4 et 8) introduits au sens large en France métropolitaine, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y).
235 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Prié (2017) | 22 | 6,65% | 22 | 20,37% | 18 | 17,14% | 18 | 17,14% |
Gargominy et al. (2011) | 21 | 6,34% | 19 | 17,59% | 17 | 16,19% | 17 | 16,19% |
Falkner et al. (2002) | 20 | 6,04% | 16 | 14,81% | 14 | 13,33% | 14 | 13,33% |
Griffiths & Florens (2006) | 13 | 3,93% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Welter-schultes (2012) | 11 | 3,32% | 8 | 7,41% | 8 | 7,62% | 7 | 6,67% |
Delannoye et al. (2015) | 10 | 3,02% | 6 | 5,56% | 6 | 5,71% | 6 | 5,71% |
Lamy & Pointier (2018) | 10 | 3,02% | 6 | 5,56% | 6 | 5,71% | 6 | 5,71% |
Dewarumez et al. (2011) | 8 | 2,42% | 8 | 7,41% | 8 | 7,62% | 8 | 7,62% |
Gerber (2018) | 8 | 2,42% | 7 | 6,48% | 7 | 6,67% | 6 | 5,71% |
Labat et al. (2011) | 8 | 2,42% | 6 | 5,56% | 6 | 5,71% | 6 | 5,71% |
Parpet & Gelder (2020) | 8 | 2,42% | 8 | 7,41% | 8 | 7,62% | 8 | 7,62% |
Breton (2014) | 7 | 2,11% | 6 | 5,56% | 6 | 5,71% | 5 | 4,76% |
Havlatova et al. (2015) | 7 | 2,11% | 7 | 6,48% | 7 | 6,67% | 7 | 6,67% |
Pointier & Marquet (1990) | 7 | 2,11% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Forcellini et al. (2012) | 6 | 1,81% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Karaman (1929) | 6 | 1,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Low & Tan (2011) | 6 | 1,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 6 | 1,81% | 6 | 5,56% | 6 | 5,71% | 6 | 5,71% |
Mueller (1936) | 6 | 1,81% | 6 | 5,56% | 6 | 5,71% | 6 | 5,71% |
Haynes (2001) | 5 | 1,51% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Lambert (1977) | 5 | 1,51% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Meynard (2011) | 5 | 1,51% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Mousson (1872) | 5 | 1,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1774) | 5 | 1,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Baldry (2007) | 4 | 1,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Gelder et al. (2012) | 4 | 1,21% | 4 | 3,7% | 4 | 3,81% | 4 | 3,81% |
Goulletquer (2016) | 4 | 1,21% | 4 | 3,7% | 4 | 3,81% | 4 | 3,81% |
Héritier et al. (2018) | 4 | 1,21% | 4 | 3,7% | 4 | 3,81% | 4 | 3,81% |
Lowe et al. (2007) | 4 | 1,21% | 4 | 3,7% | 4 | 3,81% | 3 | 2,86% |
Massemin et al. (2009) | 4 | 1,21% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Russell et al. (2021) | 4 | 1,21% | 4 | 3,7% | 4 | 3,81% | 4 | 3,81% |
Amoros (1980) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Balvay (2009) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Bouchet & Pointier (1998) | 3 | 0,91% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Colin (1998) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Fruget & Beisel (2016) | 3 | 0,91% | 3 | 2,78% | 2 | 1,9% | 3 | 2,86% |
Gelder & Ohtaka (2000) | 3 | 0,91% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Medlock et al. (2012) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Parpet & Gelder (2018) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Pointier (2001) | 3 | 0,91% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Questel (2020) | 3 | 0,91% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Tronquet (2014) | 3 | 0,91% | 3 | 2,78% | 3 | 2,86% | 3 | 2,86% |
Bouget et al. (2019) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Christensen (2016) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Colin & Hoibian (2003) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Cowie (2000) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Denis et al. (1983) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Denux & Zagatti (2010) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Devin et al. (2001) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Devin et al. (2005) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Draparnaud (1805) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Férussac (1827) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Fossati & Marquet (1998) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Gould (1852) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean et al. (2021) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Hovestadt & Neckheim (2020) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Jacquet (2023) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Jourdan et al. (2014) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Justine et al. (2022) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Krupa et al. (2021) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Lorencová et al. (2021) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-Edwards (1853) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Minard et al. (2015) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Neveu (2009) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Ng et al. (2008) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Nishihira & Urabe (2020) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Noël & Guinot (2007) | 2 | 0,6% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Notteghem (1999) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Ramage (2017) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Sars (1895) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaferna (1923) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Souben et al. (2014) | 2 | 0,6% | 2 | 1,85% | 2 | 1,9% | 2 | 1,9% |
Taylor (2003) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Wetherby (1879) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Alekseev et al. (2021) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Andrusov (1897) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2019) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Arvy (1972) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Bagny et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Bangy et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Beauchamp (1947) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Benoit (1881) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Beverley-Burton (1981) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
bij de Vaate & Beisel (2011) | 1 | 0,3% | 1 | 0,93% | 0 | 0% | 1 | 0,95% |
Bollache (2004) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Borza (2012) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchard (2021) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Bourguignat (1856) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourguignat (1870) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Bousses et al. (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Brown (1994) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunet et al. (2015) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Canning et al. (1999) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Cetre-sosah et al. (2023) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Chauvel et al. (2023) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Chevreux (1908) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Chien (1970) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Chucholl & Daudey (2008) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Cochard et al. (2010) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Cochereau (1974) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Codreanu (1949) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Colas (2019) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Collas et al. (2011) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Collas et al. (2012) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Combrisson (2023) | 1 | 0,3% | 1 | 0,93% | 0 | 0% | 1 | 0,95% |
Conrad (1831) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Coomans (1967) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Correa et al. (2010) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Couteyen (2021) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
de Cristofori & Jan (1832) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Delaunay et al. (2000) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Delaunay et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Deshayes (1863) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Deuss et al. (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Devin et al. (2006) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Draparnaud (1801) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Dunker (1848) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
European Commission (2014) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Evenhuis (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Faillettaz et al. (2020) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Ferrand (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Ferrer et al. (2018) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Filipová et al. (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Fitzinger (1833) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien (1936) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Geist et al. (2022) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Gelder & Hall (1990) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Gérard et al. (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Girardi (2003) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Girod (2004) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Goodnight (1939) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Goto (1891) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1846) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1859) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Grabowski et al. (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Grube (1860) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinot et al. (2018) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Hamon (1953) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Harada (1930) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Henderson & Okamura (2004) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Hesse & Mangot (2015) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffman & Putz (1964) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Hoffman (1963) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Hohenadler et al. (2018) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Hondt & Condé (1996) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Jaureguiberry et al. (2005) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Jay et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Jeffreys (1830) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1964) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Kadolsky (2012) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kampen & Werner (2014) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kellogg (1906) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Klass et al. (2021) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kohn & Waterstraat (1990) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Kouba et al. (2014) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kruger et al. (2019) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kuschel (1951) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Kvach et al. (2020) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Laffitte et al. (2023) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Lagarde (2008) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Lankester (1880) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Lea (1834) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Leidy (1887) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescher-Moutoué (1979) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Linnaeus (1758) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeuillet et al. (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Lounnas et al. (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Lydeard et al. (2016) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyko (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Mabille (1881) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Marescaux et al. (2012) | 1 | 0,3% | 1 | 0,93% | 0 | 0% | 1 | 0,95% |
Martens et al. (2019) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin et al. (2018) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Matsuzaki et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Maury (1973) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Mazé (1883) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazé (1890) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Méhes (1939) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Meisch et al. (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Mizelle & Donahue (1944) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Mouthon & Forcellini (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Mouthon & Loiseau (2000) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Mouthon et al. (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Moutier & Moutier (1920) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël, Breton (2016) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Noël (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
OMS (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pallas (1771) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrot-minnot et al. (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pezy et al. (2015) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pigneur et al. (2011) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pinkster (1973) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Piscart et al. (2008) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pointier & Delay (1995) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Pointier et al. (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Prié & Fruget (2017) | 1 | 0,3% | 1 | 0,93% | 0 | 0% | 1 | 0,95% |
Le Coléoptériste, 7(3): 3-39. [Une mise à jour 2011 a été obtenue auprès de l'auteur.]">Queney (2004) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Questel (2014) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Quiñonero-salgado & López-soriano (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Règlement d'exécution (UE) 2016/1141 | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Renon & Pineau (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Rignault & Chevallier (2017) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Robinson (1954) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Rogers et al. (2020) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Saito et al. (2023) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Say (1817) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Say (1829) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Scalone & Rabet (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Schaffner & Karch (2000) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Schaffner et al. (2003) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Scholte & Schaffner (2007) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Scourfield (1947) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Sexton (1939) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Skuse (1895) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Sowerby (1941) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Soyer (1958) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Starmühlner (1970) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Starmühlner (1976) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Stephensen (1935) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Stephenson (1910) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Stepien et al. (2013) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Subchev (2008) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Theobald (1901) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiéry & Robert (1992) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Tronquet (2018) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Tuzet & Perrugia (1957) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandel (1922) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Vareille-Morel (1982) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Vasileva et al. (2009) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Vila et al. (2004) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Wittmann & Ariani (2000) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Yamaguchi (1933) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Yera et al. (2013) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |
Younes et al. (2021) | 1 | 0,3% | 1 | 0,93% | 1 | 0,95% | 1 | 0,95% |