Espèces animales introduites à Saint-Pierre-et-Miquelon
Animaux introduits au sens large à Saint-Pierre-et-Miquelon, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y)
349 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Linnaeus (1758) | 55 | 8,63% | 12 | 9,68% | 12 | 10,26% | 11 | 9,4% |
Noblecourt (2016) | 35 | 5,49% | 6 | 4,84% | 6 | 5,13% | 6 | 5,13% |
Tronquet (2014) | 23 | 3,61% | 23 | 18,55% | 21 | 17,95% | 23 | 19,66% |
Albouy & Richard (2017) | 19 | 2,98% | 17 | 13,71% | 17 | 14,53% | 16 | 13,68% |
Albouy et al. (2017) | 17 | 2,67% | 16 | 12,9% | 16 | 13,68% | 16 | 13,68% |
Giard (1872) | 15 | 2,35% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Hindermeyer et al. (2007) | 13 | 2,04% | 12 | 9,68% | 11 | 9,4% | 12 | 10,26% |
[Denis & Schiffermüller] (1775) | 12 | 1,88% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 11 | 1,73% | 10 | 8,06% | 9 | 7,69% | 10 | 8,55% |
Bay-nouailhat & Bay-nouailhat (2020) | 10 | 1,57% | 10 | 8,06% | 10 | 8,55% | 10 | 8,55% |
Mériguet & Zagatti (2016) | 10 | 1,57% | 10 | 8,06% | 10 | 8,55% | 9 | 7,69% |
Meurgey & Ramage (2020) | 10 | 1,57% | 10 | 8,06% | 10 | 8,55% | 10 | 8,55% |
Milne-Edwards (1841) | 10 | 1,57% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 10 | 1,57% | 9 | 7,26% | 9 | 7,69% | 8 | 6,84% |
Jourdan & Mille (2006) | 9 | 1,41% | 9 | 7,26% | 9 | 7,69% | 9 | 7,69% |
Soubeyran et al. (2011) | 9 | 1,41% | 9 | 7,26% | 9 | 7,69% | 8 | 6,84% |
Yokoyama (2013) | 9 | 1,41% | 9 | 7,26% | 9 | 7,69% | 8 | 6,84% |
Breton (2014) | 8 | 1,26% | 8 | 6,45% | 8 | 6,84% | 8 | 6,84% |
Ramage (2017) | 8 | 1,26% | 8 | 6,45% | 8 | 6,84% | 8 | 6,84% |
Sellier et al. (2016) | 8 | 1,26% | 8 | 6,45% | 8 | 6,84% | 8 | 6,84% |
Uicn et al. (2019) | 8 | 1,26% | 8 | 6,45% | 8 | 6,84% | 8 | 6,84% |
Bousquet (2012) | 7 | 1,1% | 6 | 4,84% | 5 | 4,27% | 6 | 5,13% |
Roux (1984) | 7 | 1,1% | 3 | 2,42% | 3 | 2,56% | 2 | 1,71% |
Aulagnier et al. (2017) | 6 | 0,94% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 6 | 0,94% | 6 | 4,84% | 6 | 5,13% | 6 | 5,13% |
Dominique (1892) | 6 | 0,94% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 6 | 0,94% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Leraut (1997) | 6 | 0,94% | 0 | 0% | 0 | 0% | 0 | 0% |
Leraut (2012) | 6 | 0,94% | 6 | 4,84% | 6 | 5,13% | 6 | 5,13% |
Lorvelec et al. (2007) | 6 | 0,94% | 6 | 4,84% | 6 | 5,13% | 6 | 5,13% |
Meurgey (2011) | 6 | 0,94% | 6 | 4,84% | 6 | 5,13% | 6 | 5,13% |
Bonfils (1969) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Coutanceau (2006) | 5 | 0,78% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Dominique (1902) | 5 | 0,78% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Frenot et al. (2005) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Godet et al. (2010) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Lacoste (de) (2020) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 2 | 1,71% |
Nelson-Smith et al. (2014) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Peck (2011) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Rageau (1958) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Theuerkauf et al. (2010) | 5 | 0,78% | 5 | 4,03% | 5 | 4,27% | 5 | 4,27% |
Audinet-Serville (1823) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré (2021) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Boyer & Rivault (2003) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Fourcroy (1785) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (1996) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Geoffroy (1762) | 4 | 0,63% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Godart & Duponchel (1834) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Hullé et al. (2018) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Jourdan (2020) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Jouveau et al. (2018) | 4 | 0,63% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lebard & Speight (2019) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Levesque & Delcroix (2018) | 4 | 0,63% | 4 | 3,23% | 3 | 2,56% | 4 | 3,42% |
Linnaeus (1761) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Reverté et al. (2023) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Séguy (1944) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Speight (2013) | 4 | 0,63% | 4 | 3,23% | 4 | 3,42% | 4 | 3,42% |
Adelski (2012) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Chapelin et al. (2012) | 3 | 0,47% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Chartois et al. (2023) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Chatton & Brément (1909) | 3 | 0,47% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Chevin & Savina (2013) | 3 | 0,47% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Chown & Convey (2016) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Cochereau (1974) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Denux & Zagatti (2010) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Evenhuis (2018) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Fabricius (1781) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Geer (1774) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Hartig (1840) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1796-[1828]) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Acanthoscelides obtectus sur des plantes de Phaseolus vulgaris en plein champ. Bulletin de la Société Zoologique de France, 110: 395-402.">Jarry et al. (1985) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Leraut (2014) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Marsham (1802) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Mikkola & Honey (1993) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas (2014) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Paulian (1998) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Prévost & Mougin (1970) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Stenseth (1980) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Uicn et al. (2015) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 1 | 0,85% |
Urtizberea (2021) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 0 | 0% |
Voisin et al. (2017) | 3 | 0,47% | 3 | 2,42% | 3 | 2,56% | 3 | 2,56% |
Aulagnier (2009) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Azam (1893) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Barau et al. (2005) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 1 | 0,85% |
Beaucournu et al. (1998) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Blank & Taeger (1998) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2021) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Boisduval (1832-[1835]) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Boissel & Urtizberea (2024) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Burneleau (1983) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Butaud (2021) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Catzeflis (2018) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Chartier et al. (2007) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 0 | 0% |
Chassard-Bouchaud et al. (1985) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Clerck (1759) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Coombs & Woodroffe (1973) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Daly et al. (2023) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Daniel et al. (2020) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 0 | 0% |
Davis & Davis (2009) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Deblock et al. (1960) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Delsalle & Sechet (2014) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Dewarumez et al. (2011) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Douyer (1981) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Fauvel (1904) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Gentry et al. (2004) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Geoffroy (1762) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilot et al. (1992) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Gmelin (1789) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Goeze (1783) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2016) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Gomy (2000) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Heller (1916) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Hullé & Vernon (2021) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Iperti & Bertand (2001) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Karsholt et al. (2006) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Katsoyannos et al. (1997) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Kieffer (1898) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Koechlin (1977) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Laforgue (2015) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 1 | 0,85% |
Lafranchis (2014) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lafranchis (2016) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Le Peletier (1823) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1815-1875) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1949) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Legrand (1950) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Legrand (1953) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Levesque & Clergeau (2002) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Lindberg (1958) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Linnaeus (1767) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2011) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Meganck et al. (2017) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Miers (1878) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochs (1949) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. 2006 | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Rageau (1959) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Redon & Chorein (2009) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Remsen et al. (2013) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Rocamora (2004) | 2 | 0,31% | 2 | 1,61% | 1 | 0,85% | 2 | 1,71% |
Rognes & Blackith (1990) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Saint et al. (1978) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Sentz‐Braconnot (1966) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Sherborn & Woodward (1901) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Shinonaga et al. (1991) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Srot (1979) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Stewart (1934) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Stewart (1934) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Theodorides (1955) | 2 | 0,31% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 1 | 0,85% |
Vayssières et al. (2001) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Zahradník & Poussereau (2022) | 2 | 0,31% | 2 | 1,61% | 2 | 1,71% | 2 | 1,71% |
Zilli (2021) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Abraham (2017) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Andrieux et al. (1981) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Anonyme. (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Aubert & Beaucournu (1976) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Aubouin et al. (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Baraniak (2007) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Baylac (1980) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Beaucournu et al. (1985) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Beaucournu (1968) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanchot (1992) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Bocquet (1953) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnefoy & Marchal (1942) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Brown (1929) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Callot & Rioux (1965) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Casevitz-Weulersse & Galkowski (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Catzeflis (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Chastel et al. (1981) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Chastel et al. (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Chatton & Lwoff (1930) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Chatton & Séguéla (1936) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Cheesman (1927) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Chopard (1924) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Clark & Harrison (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Clements et al. (2015) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Clergeau & Vigne (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Coatmeur (1999) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Cochereau (1966) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Colligros & Lebecque (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Coulon et al. (2011) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Creighton (1950) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Croset et al. (1980) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1792) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dachy (1979) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Dauvin et al. (1991) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Davis & Davis (2008) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
De Geer (1773) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Deknuydt et al. (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Delacour (1963) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Delbol & Perez (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Delhaes et al. (2001) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Des et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Dewynter & Claessens (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Dubois et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Duponchel (1838-[1840]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Duponchel (1842-[1845]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2007) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Eaton et al. (1879) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Erxleben (1777) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Evenhuis (1989) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Evenhuis (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Fabre & Orsini (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Fabricius (1775) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius ([1777]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fadda (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Fischer (1925) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Fitch (1856) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Forel (1902) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fort & Barrière (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Fougère et al. (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Garrouste & Hervé (2009) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Germar (1821) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
González-Miguéns et al. (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Guegan (1970) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Guth (1971) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Hamard et al. (2013) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Hartig (1837) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Haworth (1803-1828) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hebard (1933) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Heppner (1982) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Herdman (1882) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Hinton (1941) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hipeau-Jacquotte & Coste (1989) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Hoffmann & Smith (2005) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Holloway & Peters (1976) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Honey & Scoble (2001) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Hübner (1796-[1828]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hübner (1816-[1826]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ices (2022) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Jackson (1938) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Jackson (1941) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Joannis (1915) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Julien (1881) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Kassebeer (2000) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Kiesenwetter (1851) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Klug (1816) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolenati (1846) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacourt (1985) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lambert (2004) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lancastre et al. (1976) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lauriaut et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Le Maitre & Chadee (1983) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lebas et al. (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lechapt (2015) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Leistikow & Wägele (1999) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lemoine & Quindroit (2023) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Leraut (2005) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lethierry (1881) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Letournel et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Letournel et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Bulletin de la Société d'Histoire Naturelle des Ardennes, 97: 67-69.">Ligeron (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2019) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Löbl & Smetana (2006) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Löbl & Smetana (2013) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Loxton (2017) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Lucas (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Majka & Langor (2011) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Malloch (1932) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Marcos-garcía et al. (2013) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Marion & Clergeau (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Martin et al. (2021) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Mas-Coma et al. (1989) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Mathias & Fournal (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Mayr (1861) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Meigen (1830) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Molina & Molinari (1999) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Monniot & Monniot (1983) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Monniot et al. (2011) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Monniot (1978) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Müller (1776) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Neunzig (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Neve (2015) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Nicolas (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Noblecourt (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Ochsenheimer (1808) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1790) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ooishi (2008) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Ortmann (1890) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Ouellet (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1766) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1773) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Pascal & Vigne (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Pascal et al. (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Pearman et al. (2016) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Petter (1970) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Potin (2013) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Poussereau et al. (2013) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Princis (1974) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Prous et al. (2014) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Questel (2023) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Quilici et al. (1988) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Quilici et al. (1998) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Quindroit (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Racovitza (1908) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Rageau (1956) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Remillet (1988) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Remy (1928) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Renaud et al. (2013) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Retzius (1783) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhoads (1896) | 1 | 0,16% | 1 | 0,81% | 0 | 0% | 1 | 0,85% |
Rivault et al. (1991) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Robinson & Nielsen (1983) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ronkay et al. (2017) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Ross (1819) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Rossi (1792) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Roth & Rivault (2002) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Routtier et al. (2023) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Ruzsky (1926) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Savina (2019) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Say (1831) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmalfuss (2003) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Séguy (1960) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Socolovschi et al. (2012) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Sonnini & Latreille (1801) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Stierlin (1861) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Thévenot (2014) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Thomas (2015) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Traustedt (1881) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Uicn et al. (2015) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Uicn et al. (2017) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Uicn et al. (2020) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Umble & Fisher (2000) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Umble & Fisher (2002) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Varela et al. (2007) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Villa & Villa (1833) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vivares & Sprague (1979) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Weimerskirch et al. (2009) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 0 | 0% |
Yang & Landry (2019) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Zaddach (1859) | 1 | 0,16% | 1 | 0,81% | 1 | 0,85% | 1 | 0,85% |
Zeller (1849) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |