Longicornes des Antilles françaises
Cerambycidae des îles françaises de l'arc antillais, du nord au sud : Saint-Martin, Saint-Barthélemy, Guadeloupe et Martinique.
75 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Chalumeau & Touroult (2005) | 155 | 70,45% | 133 | 106,4% | 120 | 104,35% | 132 | 112,82% |
| Peck (2011) | 113 | 51,36% | 97 | 77,6% | 87 | 75,65% | 96 | 82,05% |
| Peck et al. (2014) | 74 | 33,64% | 69 | 55,2% | 68 | 59,13% | 65 | 55,56% |
| Meurgey & Ramage (2020) | 68 | 30,91% | 66 | 52,8% | 63 | 54,78% | 63 | 53,85% |
| Peck (2011) | 68 | 30,91% | 61 | 48,8% | 50 | 43,48% | 61 | 52,14% |
| Meurgey (2011) | 66 | 30% | 58 | 46,4% | 53 | 46,09% | 58 | 49,57% |
| Touroult (2012) | 28 | 12,73% | 26 | 20,8% | 26 | 22,61% | 26 | 22,22% |
| Fleutiaux & Sallé ([1890]) | 24 | 10,91% | 10 | 8% | 10 | 8,7% | 10 | 8,55% |
| Villiers (1980) | 22 | 10% | 12 | 9,6% | 12 | 10,43% | 11 | 9,4% |
| Colijn et al. (2020) | 17 | 7,73% | 16 | 12,8% | 16 | 13,91% | 12 | 10,26% |
| Questel (2020) | 15 | 6,82% | 15 | 12% | 13 | 11,3% | 15 | 12,82% |
| Tavakilian & Chevillotte (2013) | 15 | 6,82% | 14 | 11,2% | 14 | 12,17% | 10 | 8,55% |
| Questel & Le Quellec (2012) | 14 | 6,36% | 12 | 9,6% | 10 | 8,7% | 12 | 10,26% |
| Chalumeau & Touroult (2004) | 13 | 5,91% | 7 | 5,6% | 7 | 6,09% | 7 | 5,98% |
| Villiers (1979) | 13 | 5,91% | 10 | 8% | 10 | 8,7% | 10 | 8,55% |
| Touroult et al. (2022) | 9 | 4,09% | 9 | 7,2% | 9 | 7,83% | 9 | 7,69% |
| Gahan (1895) | 7 | 3,18% | 4 | 3,2% | 4 | 3,48% | 4 | 3,42% |
| Touroult & Poirier (2021) | 7 | 3,18% | 7 | 5,6% | 7 | 6,09% | 7 | 5,98% |
| Breuning (1980) | 6 | 2,73% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Remillet (1988) | 6 | 2,73% | 5 | 4% | 5 | 4,35% | 3 | 2,56% |
| Touroult (2017) | 6 | 2,73% | 6 | 4,8% | 6 | 5,22% | 6 | 5,13% |
| Linnaeus (1758) | 5 | 2,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chalumeau & Touroult (2004) | 4 | 1,82% | 4 | 3,2% | 2 | 1,74% | 4 | 3,42% |
| Fabricius (1792) | 4 | 1,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult (2004) | 4 | 1,82% | 4 | 3,2% | 4 | 3,48% | 4 | 3,42% |
| Touroult (2007) | 4 | 1,82% | 4 | 3,2% | 4 | 3,48% | 4 | 3,42% |
| Touroult (2014) | 4 | 1,82% | 3 | 2,4% | 1 | 0,87% | 3 | 2,56% |
| Fabricius (1775) | 3 | 1,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giannoulis et al. (2014) | 3 | 1,36% | 3 | 2,4% | 3 | 2,61% | 3 | 2,56% |
| Tavakilian (1997) | 3 | 1,36% | 2 | 1,6% | 0 | 0% | 2 | 1,71% |
| Villiers (1980) | 3 | 1,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Botero et al. (2020) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chalumeau & Touroult (2004) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Chalumeau & Touroult (2005) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Delahaye (2020) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Fisher (1932) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilmour (1963) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 2 | 0,91% | 2 | 1,6% | 1 | 0,87% | 1 | 0,85% |
| Linnaeus (1767) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santos-silva & Bezark (2021) | 2 | 0,91% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Santos-Silva et al. (2010) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Santos-silva et al. (2018) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Touroult et al. (2021) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Villiers (1980) | 2 | 0,91% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villiers (1981) | 2 | 0,91% | 2 | 1,6% | 2 | 1,74% | 2 | 1,71% |
| Bezark (2015) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blair (1934) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Blair (1934) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bousquet (2018) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chalumeau (1983) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Dalens & Touroult (2007) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Fabricius (1798) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fairmaire (1881) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Fauvel (1906) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
| Fisher (1926) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Fisher (1935) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heller (1916) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
| Linnaeus (1766) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martins & Santos-silva (2012) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martins (1971) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Martins (1975) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peck (2016) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramage (2017) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Roguet (2022) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Santos-silva & Shute (2009) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Siroux (2010) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
| Siroux (2018) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
| Sudre et al. (2010) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
| Touroult et al. (2024) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Touroult (2004) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Villiers (1979) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Vitali & Rezbanyai-reser (2003) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Vitali & Touroult (2005) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 1 | 0,85% |
| Vlasak & Santos-silva (2018) | 1 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2013) | 1 | 0,45% | 1 | 0,8% | 1 | 0,87% | 0 | 0% |
