Apoïdes de Guyane
115 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Pauly et al. (2013) | 58 | 9,52% | 54 | 15,79% | 54 | 15,93% | 54 | 15,93% |
Spinola (1841) | 54 | 8,87% | 22 | 6,43% | 22 | 6,49% | 22 | 6,49% |
Amarante (2002) | 40 | 6,57% | 40 | 11,7% | 37 | 10,91% | 40 | 11,8% |
Lepeletier (1841) | 28 | 4,6% | 8 | 2,34% | 8 | 2,36% | 8 | 2,36% |
Rasmussen et al. (2007) | 19 | 3,12% | 8 | 2,34% | 8 | 2,36% | 8 | 2,36% |
Olivier (1789) | 15 | 2,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Vivallo (2019) | 15 | 2,46% | 11 | 3,22% | 11 | 3,24% | 11 | 3,24% |
Remillet (1988) | 14 | 2,3% | 11 | 3,22% | 11 | 3,24% | 10 | 2,95% |
Rasmussen & Gonzalez (2017) | 10 | 1,64% | 10 | 2,92% | 10 | 2,95% | 10 | 2,95% |
Moure (1960) | 9 | 1,48% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Kohl (1902) | 8 | 1,31% | 4 | 1,17% | 4 | 1,18% | 4 | 1,18% |
Linnaeus (1758) | 8 | 1,31% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Fabricius (1804) | 7 | 1,15% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Meurgey (2014) | 7 | 1,15% | 7 | 2,05% | 7 | 2,06% | 7 | 2,06% |
Meurgey & Dumbardon-Martial (2015) | 6 | 0,99% | 6 | 1,75% | 6 | 1,77% | 6 | 1,77% |
Meurgey & Ramage (2020) | 6 | 0,99% | 6 | 1,75% | 6 | 1,77% | 6 | 1,77% |
Roubik (1980) | 6 | 0,99% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Freitas & Oliveira (2003) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Hinojosa-Díaz & Engel (2014) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Meurgey & Dumbardon-Martial (2019) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Meurgey & Questel (2015) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Moure & Camargo (1982) | 5 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Nogueira et al. (2017) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Questel (2020) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Roubik (2004) | 5 | 0,82% | 5 | 1,46% | 5 | 1,47% | 5 | 1,47% |
Camargo & Pedro (2004) | 4 | 0,66% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
de Oliveira Andrade et al. (2022) | 4 | 0,66% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Leclercq (2002) | 4 | 0,66% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Pedro & Camargo (2003) | 4 | 0,66% | 4 | 1,17% | 4 | 1,18% | 4 | 1,18% |
Santos & Melo (2015) | 4 | 0,66% | 4 | 1,17% | 4 | 1,18% | 4 | 1,18% |
Snelling (1984) | 4 | 0,66% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
UICN Comité français, OFB & MNHN (2021) | 4 | 0,66% | 4 | 1,17% | 4 | 1,18% | 4 | 1,18% |
Camargo & Moure (1994) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Cockerell (1912) | 3 | 0,49% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Gonzalez et al. (2018) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Parker (1929) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Pierre et al. (2017) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Questel & Le Quellec (2012) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Schwarz (1932) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Yokoyama (2013) | 3 | 0,49% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Almeida (1984) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Almeida (1992) | 2 | 0,33% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bohart & Menke (1963) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Bohart (1996) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Camargo & Moure (1990) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Camargo & Pedro (2009) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Cockerell (1926) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Engel & Brooks (1998) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Engel & Brooks (2000) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Fabricius (1775) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Freitas et al. (2005) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Friese (1912) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham & Packer (2024) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Hurd (1978) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Laberge (1994) | 2 | 0,33% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Leclercq (1950) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Leclercq (2005) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Leclercq (2005) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Lepeletier & Saint-fargeau (1845) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepeletier de Saint Fargeau & Audinet-Serville (1825) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Nogueira et al. (2019) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Oliveira & Marchi (2005) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Oliveira et al. (2012) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Oliveira et al. (2024) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Parizotto & Melo (2020) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Pulawski (2010) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Smith (1854) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Vardy (1978) | 2 | 0,33% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Vicidomini (2002) | 2 | 0,33% | 2 | 0,58% | 2 | 0,59% | 2 | 0,59% |
Albouy et al. (2017) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Baker (1994) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellmann (2019) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Boyd et al. (2006) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Cameron (1888-1900) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Conte et al. (2007) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Dahlbom (1843-1845) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalla Torre (1896) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
De Geer (1773) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1898) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1793) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Friese (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Groom et al. (2016) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Jennings et al. (2013) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Jourdan & Mille (2006) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Klug (1810) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kohl (1895) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Divelec (2021) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Leclercq (1970) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey (2011) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Michener (2002) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Moure et al. (1988) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Moure (1963) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Moure (1989) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Ochoa & Oconnor (2000) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Olivier (1790-[1791]) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Praz & Bénon (2023) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Reverté et al. (2023) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Ribeiro et al. (2024) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Santiago & Moure (1999) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schomburgk (1848) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwarz (1948) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1851) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1856) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Smith (1874) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Soltani et al. (2017) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Touroult et al. (2017) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 0 | 0% |
Touroult et al. (2021) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Vachal (1907) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Vachal (1908) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Vivallo (2020) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Zakardjian et al. (2020) | 1 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |