Arbres de la Réunion
165 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) | 480 | 26.04% | 424 | 130.46% | 424 | 147.74% | 400 | 132.01% |
| Molino et al. (2022) | 284 | 15.41% | 19 | 5.85% | 19 | 6.62% | 18 | 5.94% |
| Anonyme (2014) | 204 | 11.07% | 177 | 54.46% | 177 | 61.67% | 163 | 53.8% |
| Funk et al. (2007) | 130 | 7.05% | 60 | 18.46% | 60 | 20.91% | 56 | 18.48% |
| Véron et al. (2021) | 127 | 6.89% | 121 | 37.23% | 104 | 36.24% | 110 | 36.3% |
| Hequet & Le Corre (2010) | 118 | 6.4% | 102 | 31.38% | 102 | 35.54% | 96 | 31.68% |
| Hequet et al. (2009) | 118 | 6.4% | 102 | 31.38% | 102 | 35.54% | 96 | 31.68% |
| MacKee (1994) | 118 | 6.4% | 101 | 31.08% | 101 | 35.19% | 96 | 31.68% |
| Tison et al. (2014) | 91 | 4.94% | 51 | 15.69% | 50 | 17.42% | 48 | 15.84% |
| Delnatte & Meyer (2012) | 66 | 3.58% | 56 | 17.23% | 56 | 19.51% | 51 | 16.83% |
| Molino et al. (2009) | 64 | 3.47% | 57 | 17.54% | 57 | 19.86% | 53 | 17.49% |
| Fourdrigniez & Meyer (2008) | 56 | 3.04% | 50 | 15.38% | 49 | 17.07% | 46 | 15.18% |
| Munzinger et al. (2016) | 51 | 2.77% | 20 | 6.15% | 20 | 6.97% | 18 | 5.94% |
| Morat & Veillon (1985) | 32 | 1.74% | 26 | 8% | 26 | 9.06% | 21 | 6.93% |
| Morat et al. (2012) | 32 | 1.74% | 22 | 6.77% | 22 | 7.67% | 20 | 6.6% |
| Boullet et al. (2018) | 31 | 1.68% | 30 | 9.23% | 28 | 9.76% | 28 | 9.24% |
| Ter Steege et al. (2016) | 28 | 1.52% | 24 | 7.38% | 24 | 8.36% | 24 | 7.92% |
| Acevedo-Rodríguez & Strong (2012) | 25 | 1.36% | 23 | 7.08% | 23 | 8.01% | 17 | 5.61% |
| Aublet (1775) | 20 | 1.09% | 8 | 2.46% | 8 | 2.79% | 8 | 2.64% |
| Florence (2004) | 20 | 1.09% | 18 | 5.54% | 17 | 5.92% | 18 | 5.94% |
| Sennikov & Kurtto (2017) | 19 | 1.03% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Mitchell & Daly (2015) | 18 | 0.98% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Barneby & Grimes (1996) | 16 | 0.87% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Linnaeus (1753) | 16 | 0.87% | 12 | 3.69% | 10 | 3.48% | 11 | 3.63% |
| Léotard & Chaline (2013) | 14 | 0.76% | 14 | 4.31% | 14 | 4.88% | 12 | 3.96% |
| Coode 1982 | 13 | 0.71% | 9 | 2.77% | 9 | 3.14% | 9 | 2.97% |
| Florence (1997) | 11 | 0.6% | 11 | 3.38% | 11 | 3.83% | 11 | 3.63% |
| Dorr & Wurdack (2020) | 10 | 0.54% | 2 | 0.62% | 2 | 0.7% | 1 | 0.33% |
| Lavergne (2011) | 10 | 0.54% | 9 | 2.77% | 8 | 2.79% | 8 | 2.64% |
| Miller (1768) | 10 | 0.54% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Pennington (1990) | 10 | 0.54% | 3 | 0.92% | 3 | 1.05% | 3 | 0.99% |
| Lemée (1952) | 9 | 0.49% | 5 | 1.54% | 5 | 1.74% | 5 | 1.65% |
| Stace (2010) | 9 | 0.49% | 3 | 0.92% | 3 | 1.05% | 3 | 0.99% |
| Granville & Gayot (2014) | 8 | 0.43% | 8 | 2.46% | 8 | 2.79% | 8 | 2.64% |
| Maas et al. (2023) | 8 | 0.43% | 4 | 1.23% | 4 | 1.39% | 4 | 1.32% |
| Allen et al. (2022) | 7 | 0.38% | 7 | 2.15% | 7 | 2.44% | 7 | 2.31% |
| Zerega et al. (2005) | 7 | 0.38% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Acevedo-Rodríguez (2012) | 6 | 0.33% | 4 | 1.23% | 4 | 1.39% | 4 | 1.32% |
| Gardner et al. (2021) | 6 | 0.33% | 5 | 1.54% | 5 | 1.74% | 5 | 1.65% |
| Kyalangalilwa et al. (2013) | 6 | 0.33% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Meyer et al. (2006) | 6 | 0.33% | 4 | 1.23% | 4 | 1.39% | 3 | 0.99% |
| Mitchell (1997) | 6 | 0.33% | 4 | 1.23% | 4 | 1.39% | 4 | 1.32% |
| Peraza et al. (2022) | 6 | 0.33% | 5 | 1.54% | 5 | 1.74% | 5 | 1.65% |
| Rainer (2007) | 6 | 0.33% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Salisbury (1796) | 6 | 0.33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béguinot (2012) | 5 | 0.27% | 5 | 1.54% | 5 | 1.74% | 5 | 1.65% |
| Euro+Med (2006) | 5 | 0.27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fournier (1934-1940) | 5 | 0.27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1753) | 5 | 0.27% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Pennington & Biggs (2016) | 5 | 0.27% | 4 | 1.23% | 4 | 1.39% | 4 | 1.32% |
| Tassin et al. (2006) | 5 | 0.27% | 5 | 1.54% | 5 | 1.74% | 5 | 1.65% |
| Arcangeli (1882) | 4 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Byng et al. (2016) | 4 | 0.22% | 4 | 1.23% | 4 | 1.39% | 4 | 1.32% |
| Cowan & Lindeman (1989) | 4 | 0.22% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Cuatrecasas (1964) | 4 | 0.22% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Friedmann (1997) | 4 | 0.22% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Fryxell (2001) | 4 | 0.22% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Koehne (1877) | 4 | 0.22% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Lamarck (1783) | 4 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 4 | 0.22% | 4 | 1.23% | 4 | 1.39% | 3 | 0.99% |
| Rouy & Foucaud (1897) | 4 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1913) | 4 | 0.22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yang et al. (2022) | 4 | 0.22% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Couhia & Fleurot (2016) | 3 | 0.16% | 3 | 0.92% | 3 | 1.05% | 3 | 0.99% |
| Ferlay et al. (2023) | 3 | 0.16% | 3 | 0.92% | 3 | 1.05% | 3 | 0.99% |
| Gagnon et al. (2016) | 3 | 0.16% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Gardner et al. (2021) | 3 | 0.16% | 3 | 0.92% | 3 | 1.05% | 3 | 0.99% |
| Grenier & Godron (1850) | 3 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moraes (2018) | 3 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ollitrault et al. (2020) | 3 | 0.16% | 2 | 0.62% | 0 | 0% | 2 | 0.66% |
| Richardson (1980b) | 3 | 0.16% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Song et al. (2019) | 3 | 0.16% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Souza et al. (2022) | 3 | 0.16% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Wiersema et al. (2018) | 3 | 0.16% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Alejandro et al. (2005) | 2 | 0.11% | 1 | 0.31% | 1 | 0.35% | 0 | 0% |
| Aurore et al. (2014) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| . Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béreau (2017) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berg (1992) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Bossa‐Castro et al. (2024) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Bubani & Penzig (1897) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couté & Garrouste (2009) | 2 | 0.11% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Cremers & Hoff (1998) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Jost et al. (2019) | 2 | 0.11% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Kuntze (1891) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Péchon et al. (2013) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Lourteig (1985) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muller et al. (2004) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Nyman (1882) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1792) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rohde et al. (2017) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rollet et al. (2010) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Rudd (1965) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Seigler et al. (2014) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sierra et al. (2007) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Swenson et al. (2023) | 2 | 0.11% | 2 | 0.62% | 2 | 0.7% | 2 | 0.66% |
| Allioni (1785) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allorge-Boiteau (2015) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 0 | 0% |
| Barneby et al. (2011) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boggan et al. (1992) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boggan et al. (1997) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnier & Layens (1894) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosser & Heine (2000) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Bovini (2010) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1900) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burst & Lavergne (2011) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Candolle (1845) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chavez et al. (2021) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Colli-Silva et al. (2024) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Coode (1979) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Davis et al. (2011) | 1 | 0.05% | 1 | 0.31% | 0 | 0% | 1 | 0.33% |
| Don (1831) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dorsey et al. (2013) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Ferlay et al. (2025) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Folgoat & Lavergne (2011) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Fontaine & Lavergne (2011) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Fournier (1928) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaertner (1791) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Gandoger (1875) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry (1980) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Gombauld & Duranton (1996) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Green (1988) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Green (2002) | 1 | 0.05% | 1 | 0.31% | 0 | 0% | 1 | 0.33% |
| Grose & Olmstead (2007) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Guillaumin (1936) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoffmann (1791) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hollowell et al. (2001) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaastra (1982) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krebs et al. (2004) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Lamarck (1779) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1786) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapeyrouse (1813) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemée (1953) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linan et al. (2019) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Linnaeus (1763) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowry & Plunkett (2020) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Maas & Westra (1992) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Manning (1960) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Marais (1997) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Mazine et al. (2018) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Meyer et al. (2008) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Moench (1794) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mori et al. (2002) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Pearman et al. (2020) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Peck et al. (2014) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Persoon (1807) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prance et al. (2007) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Richardson (1980) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Rivière (2003) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Rochier & Lavergne (2011) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Sachet (1962) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Sagot (1881) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Samarakoon (2015) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Schrank et al. (1789) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schrire et al. (2009) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Soares et al. (2021) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Soubeyran (2008) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson (1991) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Tison & de Foucault (2015) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toutain (1989) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 0 | 0% |
| Turner & Veldkamp (2009) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
| Villanueva-almanza et al. (2021) | 1 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zakardjian et al. (2020) | 1 | 0.05% | 1 | 0.31% | 1 | 0.35% | 1 | 0.33% |
