Odonates de Guyane
Odonata de Guyane
137 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Minot (2016) | 98 | 19,8% | 92 | 30,77% | 92 | 32,28% | 85 | 29,82% |
Meurgey & Picard (2011) | 75 | 15,15% | 69 | 23,08% | 69 | 24,21% | 69 | 24,21% |
Rochas et al. (2022) | 49 | 9,9% | 43 | 14,38% | 43 | 15,09% | 43 | 15,09% |
IUCN (2013) | 41 | 8,28% | 38 | 12,71% | 38 | 13,33% | 34 | 11,93% |
Meurgey & Ramage (2020) | 23 | 4,65% | 22 | 7,36% | 22 | 7,72% | 22 | 7,72% |
Meurgey (2011) | 23 | 4,65% | 22 | 7,36% | 22 | 7,72% | 22 | 7,72% |
UICN Comité français, OFB & MNHN (2021) | 21 | 4,24% | 20 | 6,69% | 20 | 7,02% | 20 | 7,02% |
Calvert (1909) | 14 | 2,83% | 11 | 3,68% | 10 | 3,51% | 11 | 3,86% |
Selys Longchamps (1853) | 11 | 2,22% | 8 | 2,68% | 8 | 2,81% | 8 | 2,81% |
Garrison & von Ellenrieder (2015) | 8 | 1,62% | 8 | 2,68% | 8 | 2,81% | 8 | 2,81% |
Dommanget & Papazian (2000) | 7 | 1,41% | 7 | 2,34% | 7 | 2,46% | 7 | 2,46% |
Questel & Le Quellec (2012) | 7 | 1,41% | 6 | 2,01% | 6 | 2,11% | 6 | 2,11% |
Questel (2020) | 7 | 1,41% | 6 | 2,01% | 6 | 2,11% | 6 | 2,11% |
Kirby (1897) | 5 | 1,01% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Williamson (1915) | 5 | 1,01% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Williamson (1919) | 5 | 1,01% | 4 | 1,34% | 4 | 1,4% | 4 | 1,4% |
Couteyen & Papazian (2012) | 4 | 0,81% | 4 | 1,34% | 4 | 1,4% | 4 | 1,4% |
Geijskes (1984) | 4 | 0,81% | 3 | 1% | 3 | 1,05% | 1 | 0,35% |
Machet (1990) | 4 | 0,81% | 4 | 1,34% | 4 | 1,4% | 4 | 1,4% |
Rambur (1842) | 4 | 0,81% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Selys & Longchamps (1865) | 4 | 0,81% | 4 | 1,34% | 4 | 1,4% | 4 | 1,4% |
Belle (1998) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Burmeister (1839) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Drury (1773) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleck (2017) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Garrison (2012) | 3 | 0,61% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Grand et al. (2014) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Juillerat (2007) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Machado (1985) | 3 | 0,61% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Machet (1989) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Marmels & Racenis (1982) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Martin (1898) | 3 | 0,61% | 1 | 0,33% | 1 | 0,35% | 0 | 0% |
Minot & Gaschignard (2017) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Papazian (2002) | 3 | 0,61% | 3 | 1% | 3 | 1,05% | 3 | 1,05% |
Aguesse & Gaillot (1969) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
De Marmels (1992) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Ellenrieder (2013) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Fleck & Juillerat (2019) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Fleck (2003) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 1 | 0,35% |
Garrison & von Ellenrieder (2009) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Garrouste & Hervé (2009) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Gloyd (1973) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Grand et al. (2019) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Heidemann & Seidenbusch (2002) | 2 | 0,4% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lagarde (2008) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Leonard (1977) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Linnaeus (1758) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Machado (2009) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Machet (1990) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Martiré (2010) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Meurgey & Poiron (2012) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Meurgey (2004) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Meurgey (2004) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Neiss & Marmels (2017) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Sjöstedt (1918) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Tennessen et al. (2017) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Tennessen (2009) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Touroult (2015) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Uicn et al. (2020) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Vargas et al. (2013) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Westfall (1988) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Williamson & Williamson (1924) | 2 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Williamson (1916) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Yokoyama (2013) | 2 | 0,4% | 2 | 0,67% | 2 | 0,7% | 2 | 0,7% |
Belle (1971) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Belle (1972) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Belle (1989) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Belle (1992) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bick & Bick (1985) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Brauer (1865) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Calvert (1913) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Cheesman (1927) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Clastrier & Legrand (1990) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Costa & Garrison (2001) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Coupry & Nepoux (2006) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Couteyen & Papazian (2007) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Daumal (2013) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
De Geer (1773) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Devaud & Lebouvier (2019) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Dijkstra et al. (2015) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Doucet (2016) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Dupont (2000) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Duquef & Salack (2010) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Ellenrieder & Von (2009) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Fabricius ([1777]) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Forster (1905) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrison & Costa (2002) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Garrison & Ellenrieder (2024) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Garrison et al. (2006) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Garrison (1997) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrison (2014) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Geijskes (1971) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Grand & Boudot (2007) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Grand et al. (2014) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Grand (2000) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Grand (2010) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Gutierrez (1981) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Hedlund et al. (2020) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Kirby (1890) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat (2023) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lambret & Deschamps (2013) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lencioni (2022) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Leonard (1977) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lieftinck (1966) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lieftinck (1975) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lorenzo-Carballa et al. (2020) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Luglia et al. (2014) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Machet & Duquef (2004) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Marinov et al. (2016) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Marinov et al. (2019) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Marinov et al. (2021) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Marmels (1984) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 0 | 0% |
Martin (1906) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Meurgey & Weber (2005) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Meurgey & Weber (2007) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Meurgey & Williamson (2002) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Meurgey (2002) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Meurgey (2004) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Needham (1933) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1792) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinia, 18(3): 113-115.">Papazian & Duquef (2002) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Papazian et al. (2007) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Ramage (2017) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Ris (1915) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Samways (2003) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Selys & Longchamps (1862) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys & Longchamps (1862) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys & Longchamps (1877) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys Longchamps (1839) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys Longchamps (1876) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Selys Longchamps (1886) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Tennessen (1997) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Tennessen (2004) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaillant (2000) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Von & Ellenrieder (2014) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Von Ellenrieder (2008) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Ware et al. (2007) | 1 | 0,2% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |