Espèces signalées par erreur de Nouvelle-Calédonie
296 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fricke et al. (2011) | 72 | 11,41% | 65 | 30,66% | 64 | 30,92% | 65 | 31,25% |
Thouvenot et al. (2011) | 44 | 6,97% | 13 | 6,13% | 13 | 6,28% | 13 | 6,25% |
Fricke et al. (2009) | 21 | 3,33% | 16 | 7,55% | 16 | 7,73% | 16 | 7,69% |
Orchard (2013) | 18 | 2,85% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Wickel & Jamon (2010) | 14 | 2,22% | 12 | 5,66% | 12 | 5,8% | 12 | 5,77% |
Thouvenot (2023) | 12 | 1,9% | 7 | 3,3% | 7 | 3,38% | 7 | 3,37% |
Bauer & Sadlier (2000) | 11 | 1,74% | 10 | 4,72% | 10 | 4,83% | 10 | 4,81% |
Heller (1916) | 11 | 1,74% | 7 | 3,3% | 6 | 2,9% | 7 | 3,37% |
Kulbicki (comm. pers., 2011) | 11 | 1,74% | 8 | 3,77% | 8 | 3,86% | 8 | 3,85% |
Siu et al. (2017) | 10 | 1,58% | 9 | 4,25% | 9 | 4,35% | 9 | 4,33% |
Thouvenot & Bardat (2010) | 8 | 1,27% | 7 | 3,3% | 7 | 3,38% | 7 | 3,37% |
Allen (comm. pers., 2009) | 7 | 1,11% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Fricke et al. (2013) | 7 | 1,11% | 6 | 2,83% | 5 | 2,42% | 6 | 2,88% |
Sukkharak & Gradstein (2014) | 7 | 1,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ducarme (2023) | 6 | 0,95% | 6 | 2,83% | 6 | 2,9% | 6 | 2,88% |
Fauvel (1862) | 6 | 0,95% | 0 | 0% | 0 | 0% | 0 | 0% |
Grand et al. (2019) | 6 | 0,95% | 6 | 2,83% | 6 | 2,9% | 6 | 2,88% |
Ramage (2017) | 6 | 0,95% | 5 | 2,36% | 5 | 2,42% | 5 | 2,4% |
Uthicke et al. (2004) | 6 | 0,95% | 6 | 2,83% | 6 | 2,9% | 6 | 2,88% |
Williams et al. (2006) | 6 | 0,95% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Bacchet et al. (2007) | 5 | 0,79% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Chabanet & Durville (2005) | 5 | 0,79% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Fauvel (1867) | 5 | 0,79% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Jourdan & Mille (2006) | 5 | 0,79% | 5 | 2,36% | 5 | 2,42% | 5 | 2,4% |
Keith et al. (2006) | 5 | 0,79% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Lamy & Pointier (2018) | 5 | 0,79% | 5 | 2,36% | 5 | 2,42% | 5 | 2,4% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 5 | 0,79% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mille et al. (2016) | 5 | 0,79% | 5 | 2,36% | 5 | 2,42% | 5 | 2,4% |
O’Shea (2006) | 5 | 0,79% | 5 | 2,36% | 5 | 2,42% | 5 | 2,4% |
Polanco & Acero (2016) | 5 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Sukkharak & Gradstein (2017) | 5 | 0,79% | 2 | 0,94% | 1 | 0,48% | 1 | 0,48% |
Dupérré (2023) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Engel (2014) | 4 | 0,63% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fauvel (1903) | 4 | 0,63% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Fauvel (1903) | 4 | 0,63% | 3 | 1,42% | 2 | 0,97% | 3 | 1,44% |
Feliciano et al. (2021) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Fournet (2002) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Jay et al. (2009) | 4 | 0,63% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Lieftinck (1975) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Mazancourt et al. (2019) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Nattier et al. (2015) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Poupin (2010) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Tronquet (2014) | 4 | 0,63% | 4 | 1,89% | 4 | 1,93% | 4 | 1,92% |
Trouessart (1898) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Alonso et al. (2016) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Béarez & Bouffandeau (2019) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Bidgrain (2015) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Cooper et al. (2013) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Deuss et al. (2013) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fauvel (1882) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Frahm (1990) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Grand et al. (2014) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Héros et al. (2007) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Houart et al. (2015) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Ineich (2016) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Jourdan (2020) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Kronen et al. (2008) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Kulbicki et al. (2000) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Linnaeus (1758) | 3 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Maxwell et al. (2021) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Mazancourt et al. (2019) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Montrouzier (1855) | 3 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 3 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2020) | 3 | 0,48% | 3 | 1,42% | 3 | 1,45% | 3 | 1,44% |
Söderström et al. (2013) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sun et al. (2018) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Thouvenot & Bardat (2013) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Thouvenot et al. (2018) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Viette (1949) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 1 | 0,48% |
Vink (2002) | 3 | 0,48% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Yu & Jia (2015) | 3 | 0,48% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Albouy & Richard (2017) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Alonso et al. (2018) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Alonso et al. (2019) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Améziane (2007) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Beenen (2008) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Bouchet et al. (2008) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Brindle (1976) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Cernohorsky (1981) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Choy & Marquet (2002) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Cocco (1833) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Conand et al. (2010) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
De Mazancourt et al. (2018) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Eriksson et al. (2010) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Fauvel (1883) | 2 | 0,32% | 2 | 0,94% | 1 | 0,48% | 2 | 0,96% |
Fauvel (1903) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fauvel (1903) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Fossati et al. (2002) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Guille et al. (1986) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Jelinek & Lason (2018) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Jennings et al. (2013) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 1 | 0,48% |
Keith et al. (2013) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Last et al. (2016) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Legand (1950) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mary (2017) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Monod (2011) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Montrouzier (1860) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Moulds (2012) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Munzinger et al. (2016) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (2012) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Palacký (1898) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulin (1987) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Perroud & Montrouzier (1864) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Polhemus & Herring (1970) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Questel (2020) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Rageau (1956) | 2 | 0,32% | 2 | 0,94% | 2 | 0,97% | 2 | 0,96% |
Rageau (1958) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Roux (1913) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Linzer Biologische Beitraege, 41(1): 767-801. ">Schöller (2009) |
2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Smith (1997) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Sollman (2000) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Vachal (1907) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang et al. (2014) | 2 | 0,32% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Abhaya & Probst (2003) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Angel (1935) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Asthana & Sahu (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Azevedo et al. (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bailey et al. (2023) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bath (2004) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Béarez et al. (2017) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Berland & Bernard (1938) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Berland (1934) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1942) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanc et al. (1993) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Borsa et al. (2013) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Bosserelle et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bouget et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bourmaud (2003) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Carpenter & Brown (2021) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Cazanove (2022) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Cheesman (1927) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Cheke (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Chûjô (1964) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Cohic (1950) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette (2003) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Conand et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Corporaal (1937) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Damoiseau (1966) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Delrieu-Trottin et al. (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Denux & Zagatti (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Deshayes (1863) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Dierkens & Charlat (2011) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dierkens (2021) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Distant (1914) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Distant (1920) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Distant (1920) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dmitriev (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Duméril & Duméril (1851) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril et al. (1854) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Emery (1914) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Černý (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fabricius (1775) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1889) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1891) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fauvel (1904) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fedosov & Puillandre (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fiori (1894) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourdrigniez & Meyer (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Frahm et al. (1985) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
França et al. (2024) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Franco et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Galkowski (2016) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Germain et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Gill (2004) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Golestani et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Gomy (2000) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
González-sánchez et al. (2021) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Gradstein & Ilkiu-Borges (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1861) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutierrez (1981) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hancock (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Havery et al. (2018) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hendrich & van Vondel (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hendrich et al. (2010) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Hequet & Le Corre (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hequet et al. (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hernando & Ribera (2010) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hervé (2010) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Daszkiewicz (2001) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hoffmann (1890) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Massary (1997) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ineich et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
IUCN (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Jaffe & Lattke (1994) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Jiroux & Bouyon (2018) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Johnson (2001) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Jouveau et al. (2018) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kantor et al. (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Karny (1914) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kaszab (1982) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Keferstein (1867) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Keith & Vigneux (2002) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Keith et al. (1999) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Keith et al. (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Keith et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kejval (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kiesenwetter (1851) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirejtshuk (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kiszka et al. (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kolibáč (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Kool (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Lachaud et al. (2012) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Lachlan (2004) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Lamarck (1801) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ledoux & Hallé (1995) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Leponce et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Letourneur & Maggiorani (1995) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Lichtenstein (1873) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Lorvelec & Pascal (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
MacKee (1994) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Linzer Biologische Beitraege, 44(1): 591-594. ">Madl (2012) |
1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Marinov et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Matile-Ferrero & Etienne (2006) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mazur (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mcevey & Schiffer (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Meagher (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mériguet & Zagatti (2016) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Meurgey & Ramage (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Meurgey (2011) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Meyen (1834) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Michenet & Bosserelle (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mille (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Morat et al. (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Morelon (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Müller & Henle (1841) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller et al. (2016) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mulochau & Conand (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Myers (1926) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Nentwig et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Nishimura (1985) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Nolf & Hubrecht (2022) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ortea et al. (2018) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Otte et al. (1987) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Pauly et al. (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Pelorce & Hoarau (comm. pers., 2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1869) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1877) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezold & Larson (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Pinault et al. (2013) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Platnick (1993) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pleijel (2007) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Pocock (1898) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Journal of the Australian Entomological Society, 26: 209-214. ">Polhemus & Polhemus (1987) |
1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ponel & Roge (2000) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Jelínek, J. & Audisio, P. 2011. A new species of Amystrops Reitter, 1875, and an updated checklist of the Nitidulidae from Réunion Island (Coleoptera). Bulletin de la Société entomologique de France, 116(4): 421-428. ">Poussereau et al. (2011) |
1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Probst & Deso (2001) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Probst et al. (2022) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Probst (2001) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Quah & Grismer (2024) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Queney (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Questel & Le Quellec (2012) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Rafinesque Schmaltz (1810) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage et al. (2023) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ramage (2024) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Reid & Beatson (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Renner (2016) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Richling (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ris (1915) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ronot (2007) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Roux (1926) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Samuelson (1973) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sanchez & Probst (2016) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sanchez et al. (2019) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sanchez (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sato (1966) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Saussure (de) (1852) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Séneca & Söderström (2011) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Séret (1997) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Séret (2014) | 1 | 0,16% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Shaw (1802) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Solem (1961) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Sukkharak (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Tea & Larson (2023) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Tenorio (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Theischinger et al. (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Thouvenot (2015) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Tirvengadum & Bour (1985) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Tixier (1986) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Tröndlé & Boutet (2009) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Uicn et al. (2017) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Waltl (1838) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2000) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Wantiez (2001) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Wigginton (2009) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Willemse (1923) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Zakardjian et al. (2023) | 1 | 0,16% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |