Coléoptères de Saint-Barthélemy
Coleoptera de Saint-Barthélemy
166 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Peck (2011) | 186 | 60,19% | 162 | 135% | 157 | 135,34% | 162 | 139,66% |
Peck (2011) | 114 | 36,89% | 100 | 83,33% | 97 | 83,62% | 100 | 86,21% |
Meurgey (2011) | 105 | 33,98% | 62 | 51,67% | 61 | 52,59% | 62 | 53,45% |
Questel (2020) | 100 | 32,36% | 95 | 79,17% | 92 | 79,31% | 94 | 81,03% |
Meurgey & Ramage (2020) | 86 | 27,83% | 83 | 69,17% | 83 | 71,55% | 81 | 69,83% |
Peck et al. (2014) | 82 | 26,54% | 71 | 59,17% | 71 | 61,21% | 69 | 59,48% |
Questel & Le Quellec (2012) | 62 | 20,06% | 54 | 45% | 52 | 44,83% | 54 | 46,55% |
Colijn et al. (2020) | 55 | 17,8% | 51 | 42,5% | 51 | 43,97% | 47 | 40,52% |
Peck (2016) | 49 | 15,86% | 47 | 39,17% | 47 | 40,52% | 47 | 40,52% |
Chalumeau & Touroult (2005) | 40 | 12,94% | 33 | 27,5% | 29 | 25% | 33 | 28,45% |
Soldati & Touroult (2014) | 37 | 11,97% | 35 | 29,17% | 35 | 30,17% | 35 | 30,17% |
Shpeley et al. (2017) | 19 | 6,15% | 17 | 14,17% | 17 | 14,66% | 17 | 14,66% |
Chassain & Touroult (2012) | 16 | 5,18% | 11 | 9,17% | 11 | 9,48% | 11 | 9,48% |
Poussereau et al. (2018) | 16 | 5,18% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Lucas (2012) | 14 | 4,53% | 14 | 11,67% | 14 | 12,07% | 14 | 12,07% |
Nicolas (2012) | 13 | 4,21% | 13 | 10,83% | 13 | 11,21% | 13 | 11,21% |
Fleutiaux & Sallé ([1890]) | 12 | 3,88% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Heller (1916) | 8 | 2,59% | 5 | 4,17% | 5 | 4,31% | 4 | 3,45% |
Touroult (2005) | 8 | 2,59% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Ramage (2017) | 7 | 2,27% | 7 | 5,83% | 7 | 6,03% | 7 | 6,03% |
Tronquet (2014) | 7 | 2,27% | 7 | 5,83% | 7 | 6,03% | 7 | 6,03% |
Villiers (1980) | 7 | 2,27% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Gomy (2000) | 6 | 1,94% | 5 | 4,17% | 5 | 4,31% | 5 | 4,31% |
Hart & Ivie (2016) | 6 | 1,94% | 5 | 4,17% | 5 | 4,31% | 5 | 4,31% |
Touroult (2012) | 6 | 1,94% | 5 | 4,17% | 5 | 4,31% | 5 | 4,31% |
Yokoyama (2013) | 6 | 1,94% | 6 | 5% | 6 | 5,17% | 6 | 5,17% |
Dheurle (2012) | 5 | 1,62% | 5 | 4,17% | 2 | 1,72% | 5 | 4,31% |
Dupuis & Perrin (2020) | 5 | 1,62% | 4 | 3,33% | 4 | 3,45% | 3 | 2,59% |
Fabricius (1775) | 5 | 1,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 5 | 1,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Hielkema & Hielkema (2019) | 5 | 1,62% | 4 | 3,33% | 3 | 2,59% | 4 | 3,45% |
Marquet & Roguet (2003) | 5 | 1,62% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Remillet (1988) | 5 | 1,62% | 5 | 4,17% | 5 | 4,31% | 5 | 4,31% |
Rheinheimer (2014) | 5 | 1,62% | 5 | 4,17% | 5 | 4,31% | 5 | 4,31% |
Villiers (1979) | 5 | 1,62% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Bonadona (1981) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Bousquet et al. (2018) | 4 | 1,29% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Chalumeau & Touroult (2004) | 4 | 1,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalumeau (1983) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Constantin (2012) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Erwin (1991) | 4 | 1,29% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Fauvel (1903) | 4 | 1,29% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Jourdan (2020) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 3 | 2,59% |
Lemaire (2017) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Rheinheimer (2012) | 4 | 1,29% | 4 | 3,33% | 4 | 3,45% | 4 | 3,45% |
Arrow (1927) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Chassain & Sautière (2007) | 3 | 0,97% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Dejean (1825) | 3 | 0,97% | 0 | 0% | 0 | 0% | 0 | 0% |
Denux & Zagatti (2010) | 3 | 0,97% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Fauvel (1903) | 3 | 0,97% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Girón & Franz (2012) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Gonzales et al. (2014) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Ivie & Geiser (2014) | 3 | 0,97% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Jourdan & Mille (2006) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Keller & Branham (2021) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Konstantinov et al. (2022) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Linnaeus (1758) | 3 | 0,97% | 0 | 0% | 0 | 0% | 0 | 0% |
Mantilleri (2014) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Moore et al. (2018) | 3 | 0,97% | 3 | 2,5% | 2 | 1,72% | 3 | 2,59% |
Nattier et al. (2015) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Parnaudeau (2017) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Ponchel (2011) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 2 | 1,72% |
Ratcliffe & Cave (2015) | 3 | 0,97% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Schoenherr (1836) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 3 | 2,59% |
Tavakilian & Chevillotte (2013) | 3 | 0,97% | 3 | 2,5% | 3 | 2,59% | 1 | 0,86% |
Ardoin (1977) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Balazuc & Chalumeau (1978) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Ball & Shpeley (2009) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Balthasar (1966) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Blackwelder (1943) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Botero et al. (2020) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouget et al. (2019) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Bousquet (2012) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Cassola (2011) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 1 | 0,86% |
Chalumeau & Touroult (2004) | 2 | 0,65% | 2 | 1,67% | 0 | 0% | 2 | 1,72% |
Chazeau et al. (1974) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Chazeau (1978) | 2 | 0,65% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Chevrolat (1879) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Dobson (1954) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Etienne et al. (2018) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Fabricius (1781) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1801) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1867) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilmour (1963) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomy et al. (2016) | 2 | 0,65% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Gutierrez (1981) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Hartmann et al. (2021) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Lemaire (2014) | 2 | 0,65% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Linnaeus (1767) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1860) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1861) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicolas et al. (2015) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Prudhomme (2022) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Schönherr (1806) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2020) | 2 | 0,65% | 2 | 1,67% | 2 | 1,72% | 2 | 1,72% |
Villiers (1980) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
Albuquerque et al. (2014) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Alonso (2019) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Bates (1878) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellifa et al. (2017) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Bertrand (1949) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Bielawski (1973) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Borowiec & Moragues (2005) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Casey (1924) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Chalumeau (1982) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Chassain (2005) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Clément (2021) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Cochereau (1966) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Constantin et al. (2017) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Constantin (2021) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Dalens & Touroult (2007) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Damoiseau (1966) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Denier (1922) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Duranton (2004) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Fabricius ([1777]) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1792) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Fall (1910) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1906) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 0 | 0% |
Fisher (1932) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy (1762) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Giannoulis et al. (2014) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Giron et al. (2018) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Gonzalez & Vetrovec (2021) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Hammes & Putoa (1986) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Háva (2022) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Herbst ([1791]-1792) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Ivie & Hart (2016) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Leng & Mutchler (1916) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesne (1901) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
López-García & Deloya (2022) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Malausa (1977) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Martins (1971) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Meurgey (2014) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2017) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Motschulsky (1858) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Naviaux (2007) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulian (1991) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Paulian (1998) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Ponchel (2015) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 0 | 0% |
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 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Le Coléoptériste, 7(3): 3-39. [Une mise à jour 2011 a été obtenue auprès de l'auteur.]">Queney (2004) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Questel (2022) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Ramage (2015) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Ratcliffe (1976) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Reiche ([1843]) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Rheinheimer (2015) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Santos-Silva et al. (2010) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Siroux (2010) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 0 | 0% |
Siroux (2015) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Siroux (2018) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 0 | 0% |
Sudre et al. (2010) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 0 | 0% |
Touroult et al. (2015) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Touroult et al. (2016) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Touroult et al. (2021) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Touroult et al. (2022) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Touroult et al. (2022) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Tronquet (2016) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Villiers (1980) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitali & Touroult (2005) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Vorst (2008) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Weise (1885) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Zagatti & Guy (2005) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |
Zimmerman (1968) | 1 | 0,32% | 1 | 0,83% | 1 | 0,86% | 1 | 0,86% |