Arbres de Mayotte
98 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Fournet (2002) | 332 | 36,52% | 296 | 140,28% | 296 | 148% | 288 | 142,57% |
| Molino et al. (2022) | 230 | 25,3% | 13 | 6,16% | 13 | 6,5% | 12 | 5,94% |
| Funk et al. (2007) | 84 | 9,24% | 46 | 21,8% | 45 | 22,5% | 44 | 21,78% |
| Hequet & Le Corre (2010) | 71 | 7,81% | 61 | 28,91% | 61 | 30,5% | 59 | 29,21% |
| Hequet et al. (2009) | 71 | 7,81% | 61 | 28,91% | 61 | 30,5% | 59 | 29,21% |
| MacKee (1994) | 70 | 7,7% | 60 | 28,44% | 60 | 30% | 58 | 28,71% |
| Anonyme (2014) | 62 | 6,82% | 50 | 23,7% | 50 | 25% | 48 | 23,76% |
| Delnatte & Meyer (2012) | 52 | 5,72% | 46 | 21,8% | 46 | 23% | 45 | 22,28% |
| Molino et al. (2009) | 49 | 5,39% | 44 | 20,85% | 44 | 22% | 43 | 21,29% |
| Véron et al. (2021) | 48 | 5,28% | 47 | 22,27% | 45 | 22,5% | 46 | 22,77% |
| Fourdrigniez & Meyer (2008) | 45 | 4,95% | 40 | 18,96% | 39 | 19,5% | 38 | 18,81% |
| Munzinger et al. (2016) | 43 | 4,73% | 19 | 9% | 19 | 9,5% | 19 | 9,41% |
| Boullet et al. (2018) | 33 | 3,63% | 32 | 15,17% | 32 | 16% | 31 | 15,35% |
| Morat et al. (2012) | 31 | 3,41% | 20 | 9,48% | 20 | 10% | 20 | 9,9% |
| Morat & Veillon (1985) | 29 | 3,19% | 25 | 11,85% | 25 | 12,5% | 24 | 11,88% |
| Gardner et al. (2021) | 21 | 2,31% | 7 | 3,32% | 7 | 3,5% | 6 | 2,97% |
| Aublet (1775) | 18 | 1,98% | 8 | 3,79% | 8 | 4% | 8 | 3,96% |
| Acevedo-Rodríguez & Strong (2012) | 17 | 1,87% | 15 | 7,11% | 15 | 7,5% | 15 | 7,43% |
| Florence (2004) | 16 | 1,76% | 15 | 7,11% | 15 | 7,5% | 15 | 7,43% |
| Ter Steege et al. (2016) | 16 | 1,76% | 15 | 7,11% | 15 | 7,5% | 15 | 7,43% |
| Barneby & Grimes (1996) | 13 | 1,43% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Tison et al. (2014) | 13 | 1,43% | 8 | 3,79% | 8 | 4% | 6 | 2,97% |
| Léotard & Chaline (2013) | 11 | 1,21% | 11 | 5,21% | 11 | 5,5% | 10 | 4,95% |
| Florence (1997) | 9 | 0,99% | 9 | 4,27% | 8 | 4% | 9 | 4,46% |
| Stace (2010) | 9 | 0,99% | 3 | 1,42% | 3 | 1,5% | 3 | 1,49% |
| Allen et al. (2022) | 8 | 0,88% | 8 | 3,79% | 8 | 4% | 8 | 3,96% |
| Maas et al. (2023) | 8 | 0,88% | 4 | 1,9% | 4 | 2% | 4 | 1,98% |
| Mitchell & Daly (2015) | 8 | 0,88% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Pennington (1990) | 8 | 0,88% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Lavergne (2011) | 7 | 0,77% | 6 | 2,84% | 6 | 3% | 5 | 2,48% |
| Miller (1768) | 7 | 0,77% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Zerega et al. (2005) | 7 | 0,77% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Byng et al. (2016) | 6 | 0,66% | 5 | 2,37% | 5 | 2,5% | 5 | 2,48% |
| Lemée (1952) | 6 | 0,66% | 3 | 1,42% | 3 | 1,5% | 3 | 1,49% |
| Rainer (2007) | 6 | 0,66% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Pennington & Biggs (2016) | 5 | 0,55% | 4 | 1,9% | 4 | 2% | 4 | 1,98% |
| Cowan & Lindeman (1989) | 4 | 0,44% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Cuatrecasas (1964) | 4 | 0,44% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Fryxell (2001) | 4 | 0,44% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Granville & Gayot (2014) | 4 | 0,44% | 4 | 1,9% | 4 | 2% | 4 | 1,98% |
| Linnaeus (1753) | 4 | 0,44% | 4 | 1,9% | 3 | 1,5% | 3 | 1,49% |
| Linnaeus (1753) | 4 | 0,44% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Meyer et al. (2006) | 4 | 0,44% | 3 | 1,42% | 3 | 1,5% | 2 | 0,99% |
| Mitchell (1997) | 4 | 0,44% | 3 | 1,42% | 3 | 1,5% | 3 | 1,49% |
| Bidault et al. (2024) | 3 | 0,33% | 3 | 1,42% | 3 | 1,5% | 3 | 1,49% |
| Kyalangalilwa et al. (2013) | 3 | 0,33% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Ollitrault et al. (2020) | 3 | 0,33% | 2 | 0,95% | 0 | 0% | 2 | 0,99% |
| Souza et al. (2022) | 3 | 0,33% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Stevens et al. (2016) | 3 | 0,33% | 3 | 1,42% | 3 | 1,5% | 3 | 1,49% |
| Werff & Henk (2013) | 3 | 0,33% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Acevedo-Rodríguez (2012) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Aurore et al. (2014) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béreau (2017) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berg (1992) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Bossa‐Castro et al. (2024) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Couhia & Fleurot (2016) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Couté & Garrouste (2009) | 2 | 0,22% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Fosberg (1937) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardner et al. (2021) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Gargominy et al. (1996) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Jost et al. (2019) | 2 | 0,22% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Lowe et al. (2007) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 1 | 0,5% |
| Peraza et al. (2022) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Ricketson & Pipoly (2013) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Song et al. (2019) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Swenson et al. (2023) | 2 | 0,22% | 2 | 0,95% | 2 | 1% | 2 | 0,99% |
| Allorge-Boiteau (2015) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Barthelat (2019) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Berg (1972) | 1 | 0,11% | 1 | 0,47% | 0 | 0% | 1 | 0,5% |
| Bosser & Heine (2000) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Bovini (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1845) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colli-Silva et al. (2024) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Don (1831) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferlay et al. (2023) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Fournier (1934-1940) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry (1980) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Guillaumin (1936) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1798) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Linnaeus (1763) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lobreau-callen (1975) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowry & Plunkett (2020) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Maas & Westra (1992) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mackinder et al. (2016) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Mazine et al. (2018) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Meyer et al. (2008) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Moench (1794) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peck et al. (2014) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Persoon (1807) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prance et al. (2007) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Richard (1792) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sachet (1962) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Sagot (1881) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Soubeyran (2008) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toutain (1989) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Turner & Veldkamp (2009) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
| Wiersema et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zakardjian et al. (2020) | 1 | 0,11% | 1 | 0,47% | 1 | 0,5% | 1 | 0,5% |
