Odonates de la Réunion
Odonata de la Réunion
66 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Couteyen & Papazian (2012) | 36 | 46,15% | 36 | 128,57% | 33 | 137,5% | 31 | 129,17% |
| Martiré (2010) | 21 | 26,92% | 20 | 71,43% | 17 | 70,83% | 19 | 79,17% |
| Lagarde (2008) | 20 | 25,64% | 19 | 67,86% | 16 | 66,67% | 18 | 75% |
| Couteyen (2009) | 13 | 16,67% | 13 | 46,43% | 13 | 54,17% | 12 | 50% |
| Meurgey & Picard (2011) | 10 | 12,82% | 10 | 35,71% | 10 | 41,67% | 10 | 41,67% |
| Grand et al. (2014) | 8 | 10,26% | 8 | 28,57% | 8 | 33,33% | 8 | 33,33% |
| Grand et al. (2019) | 7 | 8,97% | 7 | 25% | 7 | 29,17% | 7 | 29,17% |
| Forcellini et al. (2012) | 5 | 6,41% | 5 | 17,86% | 3 | 12,5% | 4 | 16,67% |
| Heidemann & Seidenbusch (2002) | 5 | 6,41% | 4 | 14,29% | 4 | 16,67% | 2 | 8,33% |
| Dijkstra et al. (2015) | 4 | 5,13% | 4 | 14,29% | 4 | 16,67% | 2 | 8,33% |
| Dijkstra (2007) | 4 | 5,13% | 4 | 14,29% | 4 | 16,67% | 4 | 16,67% |
| Doucet (2016) | 4 | 5,13% | 4 | 14,29% | 4 | 16,67% | 2 | 8,33% |
| Grand & Boudot (2007) | 4 | 5,13% | 4 | 14,29% | 4 | 16,67% | 2 | 8,33% |
| Grand et al. (2014) | 4 | 5,13% | 4 | 14,29% | 4 | 16,67% | 2 | 8,33% |
| Couteyen & Papazian (2000) | 3 | 3,85% | 3 | 10,71% | 2 | 8,33% | 3 | 12,5% |
| Grand (2004) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 3 | 12,5% |
| Marinov et al. (2019) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 3 | 12,5% |
| Meurgey & Ramage (2020) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 3 | 12,5% |
| Meurgey (2011) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 3 | 12,5% |
| Ramage (2017) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 3 | 12,5% |
| Samways (2003) | 3 | 3,85% | 3 | 10,71% | 3 | 12,5% | 2 | 8,33% |
| Campion (1913) | 2 | 2,56% | 2 | 7,14% | 0 | 0% | 2 | 8,33% |
| Cheesman (1927) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Couteyen & Papazian (2006) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Couteyen & Papazian (2008) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Couteyen & Papazian (2011) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Jolivet et al. (1999) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Kirby (1890) | 2 | 2,56% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marinov et al. (2021) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Papazian et al. (2007) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Questel & Le Quellec (2012) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Questel (2020) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Ris (1915) | 2 | 2,56% | 2 | 7,14% | 2 | 8,33% | 2 | 8,33% |
| Rochas et al. (2022) | 2 | 2,56% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Albouy et al. (2017) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 0 | 0% |
| Couteyen & Papazian (2000) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Couteyen & Papazian (2001) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 0 | 0% |
| Couteyen & Papazian (2001) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Couteyen & Papazian (2007) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Couteyen & Papazian (2011) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Darblade & Ducout (2005) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 0 | 0% |
| Daumal (2013) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Devaud & Lebouvier (2019) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Dijkstra (2005) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Grand (2004) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Grand (2010) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Gutierrez (1981) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Hedlund et al. (2020) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| IUCN (2013) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Jacquemin (1988) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Kennedy (1920) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Lambret & Deschamps (2013) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Lieftinck (1966) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Lieftinck (1975) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Machet & Duquef (2004) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Marinov et al. (2016) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Minot (2016) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Needham (1932) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Pelletier (2011) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 0 | 0% |
| Roche (1989) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 0 | 0% |
| Selys Longchamps (1839) | 1 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Selys-Longchamps (1839) | 1 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Uicn et al. (2020) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Vaillant (2000) | 1 | 1,28% | 1 | 3,57% | 1 | 4,17% | 1 | 4,17% |
| Vander & Linden (1823) | 1 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
