Membracides de Guyane
52 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Lapèze (2021) | 33 | 14,41% | 33 | 22,92% | 33 | 22,92% | 33 | 22,92% |
Boulard (1980) | 29 | 12,66% | 29 | 20,14% | 29 | 20,14% | 29 | 20,14% |
Lapèze & Lopez-Vaamonde (2024) | 29 | 12,66% | 29 | 20,14% | 29 | 20,14% | 29 | 20,14% |
Lapèze (2019) | 28 | 12,23% | 28 | 19,44% | 28 | 19,44% | 28 | 19,44% |
Fairmaire (1847) | 22 | 9,61% | 9 | 6,25% | 9 | 6,25% | 9 | 6,25% |
Sakakibara (2013) | 15 | 6,55% | 12 | 8,33% | 12 | 8,33% | 12 | 8,33% |
Broomfield (1976) | 12 | 5,24% | 12 | 8,33% | 12 | 8,33% | 12 | 8,33% |
Lapèze et al. (2022) | 11 | 4,8% | 11 | 7,64% | 11 | 7,64% | 11 | 7,64% |
Goding (1929) | 10 | 4,37% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
Creao-duarte & Sakakibara (2016) | 9 | 3,93% | 8 | 5,56% | 8 | 5,56% | 8 | 5,56% |
Fabricius (1803) | 9 | 3,93% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Laporte de Castelnau (1832) | 9 | 3,93% | 7 | 4,86% | 7 | 4,86% | 7 | 4,86% |
Albertson & Dietrich (2005) | 8 | 3,49% | 8 | 5,56% | 8 | 5,56% | 8 | 5,56% |
Sakakibara (2012) | 8 | 3,49% | 8 | 5,56% | 8 | 5,56% | 8 | 5,56% |
Boulard (2011) | 6 | 2,62% | 6 | 4,17% | 6 | 4,17% | 6 | 4,17% |
Coquebert de Montbret (1801) | 6 | 2,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapèze (2022) | 6 | 2,62% | 6 | 4,17% | 6 | 4,17% | 6 | 4,17% |
Sakakibara (1996) | 6 | 2,62% | 4 | 2,78% | 4 | 2,78% | 4 | 2,78% |
Stål (1869) | 6 | 2,62% | 6 | 4,17% | 6 | 4,17% | 6 | 4,17% |
Strümpel & Strümpel (2014) | 6 | 2,62% | 6 | 4,17% | 6 | 4,17% | 6 | 4,17% |
Fabricius (1787) | 5 | 2,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Barreira & Sakakibara (2001) | 4 | 1,75% | 4 | 2,78% | 4 | 2,78% | 4 | 2,78% |
González-mozo & Mckamey (2024) | 4 | 1,75% | 4 | 2,78% | 4 | 2,78% | 4 | 2,78% |
Cryan & Deitz (1999) | 3 | 1,31% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
De Geer (1773) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1846) | 3 | 1,31% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |
Funkhouser (1922) | 3 | 1,31% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Gonzalez-mozo & Ware (2023) | 3 | 1,31% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
Haviland (1925) | 3 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Kopp & Yonke (1979) | 3 | 1,31% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
McKamey (2023) | 3 | 1,31% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
Remillet (1988) | 3 | 1,31% | 3 | 2,08% | 3 | 2,08% | 3 | 2,08% |
Amyot & Audinet-Serville (1843) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrade (1989) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Andrade (2003) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Burmeister (1836) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Creão-Duarte & Sakakibara (1997) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Creão-duarte et al. (2005) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Creão-duarte (1999) | 2 | 0,87% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |
Flynn (2020) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Funkhouser (1935) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapèze (2022) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Linnaeus (1758) | 2 | 0,87% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |
Sakakibara (1979) | 2 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Sakakibara (2005) | 2 | 0,87% | 2 | 1,39% | 2 | 1,39% | 2 | 1,39% |
Deitz & Dietrich (1993) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1775) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Germar (1835) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapèze (2018) | 1 | 0,44% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |
Maruyama (2017) | 1 | 0,44% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |
Olivier (1792) | 1 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker (1851) | 1 | 0,44% | 1 | 0,69% | 1 | 0,69% | 1 | 0,69% |