Odonates de Mayotte
Odonata de Mayotte
55 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) | 47 | 51,09% | 47 | 117,5% | 42 | 123,53% | 44 | 129,41% |
| Martiré (2010) | 12 | 13,04% | 12 | 30% | 11 | 32,35% | 11 | 32,35% |
| Samways (2003) | 12 | 13,04% | 12 | 30% | 10 | 29,41% | 11 | 32,35% |
| Lagarde (2008) | 11 | 11,96% | 11 | 27,5% | 10 | 29,41% | 10 | 29,41% |
| Ris (1915) | 9 | 9,78% | 9 | 22,5% | 6 | 17,65% | 9 | 26,47% |
| Couteyen (2009) | 8 | 8,7% | 8 | 20% | 8 | 23,53% | 7 | 20,59% |
| Meurgey & Picard (2011) | 7 | 7,61% | 7 | 17,5% | 7 | 20,59% | 7 | 20,59% |
| Grand et al. (2014) | 6 | 6,52% | 6 | 15% | 6 | 17,65% | 6 | 17,65% |
| Grand et al. (2019) | 5 | 5,43% | 5 | 12,5% | 5 | 14,71% | 5 | 14,71% |
| Dijkstra et al. (2015) | 4 | 4,35% | 4 | 10% | 4 | 11,76% | 2 | 5,88% |
| Doucet (2016) | 4 | 4,35% | 4 | 10% | 4 | 11,76% | 2 | 5,88% |
| Grand & Boudot (2007) | 4 | 4,35% | 4 | 10% | 4 | 11,76% | 2 | 5,88% |
| Grand et al. (2014) | 4 | 4,35% | 4 | 10% | 4 | 11,76% | 2 | 5,88% |
| Grand (2004) | 4 | 4,35% | 4 | 10% | 4 | 11,76% | 4 | 11,76% |
| Heidemann & Seidenbusch (2002) | 3 | 3,26% | 3 | 7,5% | 3 | 8,82% | 2 | 5,88% |
| Marinov et al. (2019) | 3 | 3,26% | 3 | 7,5% | 3 | 8,82% | 3 | 8,82% |
| Ramage (2017) | 3 | 3,26% | 3 | 7,5% | 3 | 8,82% | 3 | 8,82% |
| Campion (1913) | 2 | 2,17% | 2 | 5% | 0 | 0% | 2 | 5,88% |
| Cheesman (1927) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Couteyen & Papazian (2009) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Forcellini et al. (2012) | 2 | 2,17% | 2 | 5% | 1 | 2,94% | 2 | 5,88% |
| Marinov et al. (2021) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Meurgey & Ramage (2020) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Meurgey (2011) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Papazian et al. (2007) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Ris (1915) | 2 | 2,17% | 2 | 5% | 2 | 5,88% | 2 | 5,88% |
| Albouy et al. (2017) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 0 | 0% |
| Berquier (2013) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Couteyen & Papazian (2000) | 1 | 1,09% | 1 | 2,5% | 0 | 0% | 1 | 2,94% |
| Couteyen & Papazian (2001) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 0 | 0% |
| Devaud & Lebouvier (2019) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Dijkstra (2005) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Dijkstra (2006) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Engler (2014) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Grand (2010) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Gutierrez (1981) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Houard (2020) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 0 | 0% |
| IUCN (2013) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Jacquemin (1988) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Kirby (1890) | 1 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lieftinck (1966) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Lieftinck (1975) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Marinov et al. (2016) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| May (2002) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Minot (2016) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Needham (1932) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Questel & Le Quellec (2012) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Questel (2020) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Rochas et al. (2022) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Sélys & Longchamos (1872) | 1 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Selys-Longchamps (1839) | 1 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sjostedt (1917) | 1 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| UICN Comité français, OFB & MNHN (2021) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Vaillant (2000) | 1 | 1,09% | 1 | 2,5% | 1 | 2,94% | 1 | 2,94% |
| Vander & Linden (1823) | 1 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
