Apoïdes de Nouvelle-Calédonie
64 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Breitkreuz et al. (2016) | 79 | 37,98% | 79 | 64,23% | 79 | 68,7% | 79 | 65,83% |
Jennings et al. (2013) | 53 | 25,48% | 49 | 39,84% | 49 | 42,61% | 47 | 39,17% |
Zakardjian et al. (2023) | 51 | 24,52% | 51 | 41,46% | 46 | 40% | 50 | 41,67% |
Pauly et al. (2013) | 22 | 10,58% | 20 | 16,26% | 14 | 12,17% | 20 | 16,67% |
Pauly et al. (2015) | 17 | 8,17% | 17 | 13,82% | 17 | 14,78% | 17 | 14,17% |
Vachal (1907) | 13 | 6,25% | 7 | 5,69% | 7 | 6,09% | 6 | 5% |
Ramage (2017) | 12 | 5,77% | 11 | 8,94% | 10 | 8,7% | 11 | 9,17% |
Pauly et al. (2013) | 11 | 5,29% | 11 | 8,94% | 11 | 9,57% | 11 | 9,17% |
Leijs et al. (2017) | 8 | 3,85% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Pauly & Munzinger (2003) | 8 | 3,85% | 5 | 4,07% | 4 | 3,48% | 5 | 4,17% |
Turner (1919) | 8 | 3,85% | 4 | 3,25% | 4 | 3,48% | 4 | 3,33% |
Groom et al. (2016) | 7 | 3,37% | 6 | 4,88% | 6 | 5,22% | 5 | 4,17% |
Ramage et al. (2015) | 7 | 3,37% | 7 | 5,69% | 7 | 6,09% | 7 | 5,83% |
Schulthess (1915) | 7 | 3,37% | 4 | 3,25% | 3 | 2,61% | 4 | 3,33% |
Zakardjian et al. (2020) | 7 | 3,37% | 7 | 5,69% | 7 | 6,09% | 6 | 5% |
Ceccolini (2023) | 6 | 2,88% | 6 | 4,88% | 6 | 5,22% | 6 | 5% |
Cheesman (1955) | 6 | 2,88% | 6 | 4,88% | 6 | 5,22% | 6 | 5% |
Cheesman (1953) | 5 | 2,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 5 | 2,4% | 4 | 3,25% | 2 | 1,74% | 3 | 2,5% |
Kuhlmann (2006) | 5 | 2,4% | 4 | 3,25% | 3 | 2,61% | 4 | 3,33% |
Madl (2014) | 5 | 2,4% | 5 | 4,07% | 5 | 4,35% | 5 | 4,17% |
Paulian (1998) | 5 | 2,4% | 5 | 4,07% | 4 | 3,48% | 5 | 4,17% |
Ascher et al. (2016) | 4 | 1,92% | 4 | 3,25% | 4 | 3,48% | 4 | 3,33% |
Jourdan (2020) | 4 | 1,92% | 4 | 3,25% | 3 | 2,61% | 4 | 3,33% |
Le Divelec (2024) | 4 | 1,92% | 4 | 3,25% | 4 | 3,48% | 4 | 3,33% |
Williams (1932) | 4 | 1,92% | 4 | 3,25% | 4 | 3,48% | 4 | 3,33% |
Krombein (1950) | 3 | 1,44% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Meurgey & Ramage (2020) | 3 | 1,44% | 3 | 2,44% | 2 | 1,74% | 2 | 1,67% |
Rageau (1958) | 3 | 1,44% | 3 | 2,44% | 1 | 0,87% | 3 | 2,5% |
Bellmann (2019) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 1 | 0,83% |
Chatthanabun et al. (2020) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Gros (2020) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Menke (1979) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Meurgey & Dumbardon-Martial (2015) | 2 | 0,96% | 2 | 1,63% | 1 | 0,87% | 1 | 0,83% |
Meurgey (2014) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 0 | 0% |
Ohl (2002) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Pulawski (1989) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Questel & Le Quellec (2012) | 2 | 0,96% | 2 | 1,63% | 1 | 0,87% | 1 | 0,83% |
Yasumatsu (1953) | 2 | 0,96% | 2 | 1,63% | 2 | 1,74% | 2 | 1,67% |
Albouy et al. (2017) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Boyd et al. (2006) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Chapelin-Viscardi & Lariviere (2014) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Cheesman (1936) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Conte et al. (2007) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Friese (1907) | 1 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan et al. (2014) | 1 | 0,48% | 1 | 0,81% | 0 | 0% | 1 | 0,83% |
Klug (1801) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Leclercq (2006) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Linnaeus (1758) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Linnaeus (1761) | 1 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Questel (2015) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Meurgey (2011) | 1 | 0,48% | 1 | 0,81% | 0 | 0% | 1 | 0,83% |
Pauly & Villemant (2009) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Pauly et al. (2001) | 1 | 0,48% | 1 | 0,81% | 0 | 0% | 1 | 0,83% |
Pierre et al. (2017) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Pulawski (2020) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Questel (2020) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Ramage (2024) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Remillet (1988) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Reverté et al. (2023) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 0 | 0% |
Saussure (1867) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Smith (1869) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |
Trunz et al. (2016) | 1 | 0,48% | 1 | 0,81% | 1 | 0,87% | 1 | 0,83% |