Arbres de Polynésie française
157 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Molino et al. (2022) | 485 | 27.23% | 30 | 9.23% | 30 | 10.99% | 29 | 9.67% |
| Fournet (2002) | 472 | 26.5% | 420 | 129.23% | 420 | 153.85% | 384 | 128% |
| Funk et al. (2007) | 181 | 10.16% | 71 | 21.85% | 69 | 25.27% | 66 | 22% |
| Munzinger et al. (2016) | 151 | 8.48% | 41 | 12.62% | 39 | 14.29% | 36 | 12% |
| Anonyme (2014) | 125 | 7.02% | 107 | 32.92% | 107 | 39.19% | 94 | 31.33% |
| Hequet & Le Corre (2010) | 125 | 7.02% | 107 | 32.92% | 106 | 38.83% | 98 | 32.67% |
| Hequet et al. (2009) | 125 | 7.02% | 107 | 32.92% | 106 | 38.83% | 98 | 32.67% |
| MacKee (1994) | 125 | 7.02% | 106 | 32.62% | 105 | 38.46% | 98 | 32.67% |
| Véron et al. (2021) | 90 | 5.05% | 86 | 26.46% | 67 | 24.54% | 82 | 27.33% |
| Molino et al. (2009) | 75 | 4.21% | 66 | 20.31% | 66 | 24.18% | 63 | 21% |
| Fourdrigniez & Meyer (2008) | 73 | 4.1% | 67 | 20.62% | 62 | 22.71% | 61 | 20.33% |
| Morat et al. (2012) | 72 | 4.04% | 44 | 13.54% | 43 | 15.75% | 38 | 12.67% |
| Delnatte & Meyer (2012) | 62 | 3.48% | 54 | 16.62% | 54 | 19.78% | 48 | 16% |
| Florence (1997) | 61 | 3.43% | 61 | 18.77% | 56 | 20.51% | 60 | 20% |
| Morat & Veillon (1985) | 55 | 3.09% | 46 | 14.15% | 46 | 16.85% | 39 | 13% |
| Tison et al. (2014) | 42 | 2.36% | 31 | 9.54% | 31 | 11.36% | 27 | 9% |
| Ter Steege et al. (2016) | 39 | 2.19% | 35 | 10.77% | 35 | 12.82% | 34 | 11.33% |
| Florence (2004) | 36 | 2.02% | 28 | 8.62% | 24 | 8.79% | 28 | 9.33% |
| Boullet et al. (2018) | 32 | 1.8% | 31 | 9.54% | 31 | 11.36% | 30 | 10% |
| Acevedo-Rodríguez & Strong (2012) | 26 | 1.46% | 22 | 6.77% | 22 | 8.06% | 13 | 4.33% |
| Aublet (1775) | 20 | 1.12% | 9 | 2.77% | 9 | 3.3% | 9 | 3% |
| Mitchell & Daly (2015) | 18 | 1.01% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Florence (1996) | 16 | 0.9% | 16 | 4.92% | 16 | 5.86% | 16 | 5.33% |
| Berg & Roselli (2005) | 13 | 0.73% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Brandbyge (1986) | 13 | 0.73% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Moore (1933) | 13 | 0.73% | 8 | 2.46% | 7 | 2.56% | 8 | 2.67% |
| Barneby & Grimes (1996) | 12 | 0.67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fryxell (2001) | 12 | 0.67% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Allen et al. (2022) | 11 | 0.62% | 11 | 3.38% | 10 | 3.66% | 9 | 3% |
| Couhia & Fleurot (2016) | 11 | 0.62% | 11 | 3.38% | 11 | 4.03% | 9 | 3% |
| Léotard & Chaline (2013) | 11 | 0.62% | 11 | 3.38% | 11 | 4.03% | 9 | 3% |
| Maas et al. (2023) | 10 | 0.56% | 5 | 1.54% | 5 | 1.83% | 5 | 1.67% |
| Méndez (2001) | 10 | 0.56% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Miller (1768) | 10 | 0.56% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| O'leary et al. (2021) | 10 | 0.56% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Kyalangalilwa et al. (2013) | 9 | 0.51% | 3 | 0.92% | 2 | 0.73% | 2 | 0.67% |
| Meyer et al. (2006) | 9 | 0.51% | 6 | 1.85% | 5 | 1.83% | 6 | 2% |
| Pennington (1990) | 9 | 0.51% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Stace (2010) | 9 | 0.51% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Linnaeus (1753) | 8 | 0.45% | 7 | 2.15% | 6 | 2.2% | 6 | 2% |
| Mori & Prance (1990) | 8 | 0.45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardner et al. (2021) | 7 | 0.39% | 6 | 1.85% | 6 | 2.2% | 5 | 1.67% |
| Granville & Gayot (2014) | 7 | 0.39% | 7 | 2.15% | 7 | 2.56% | 7 | 2.33% |
| Lavergne (2011) | 7 | 0.39% | 6 | 1.85% | 5 | 1.83% | 6 | 2% |
| Lemée (1952) | 7 | 0.39% | 4 | 1.23% | 4 | 1.47% | 4 | 1.33% |
| Moraes et al. (2010) | 7 | 0.39% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Zerega et al. (2005) | 7 | 0.39% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Acevedo-Rodríguez (2012) | 6 | 0.34% | 4 | 1.23% | 4 | 1.47% | 4 | 1.33% |
| Fosberg & Sachet (1981) | 6 | 0.34% | 6 | 1.85% | 0 | 0% | 6 | 2% |
| Mitchell (1997) | 6 | 0.34% | 4 | 1.23% | 4 | 1.47% | 4 | 1.33% |
| Moore (1940) | 6 | 0.34% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Rainer (2007) | 6 | 0.34% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Sleumer (1938) | 6 | 0.34% | 4 | 1.23% | 0 | 0% | 4 | 1.33% |
| Berg (1992) | 5 | 0.28% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Grose & Olmstead (2007) | 5 | 0.28% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Lowe et al. (2007) | 5 | 0.28% | 5 | 1.54% | 5 | 1.83% | 5 | 1.67% |
| Pennington & Biggs (2016) | 5 | 0.28% | 4 | 1.23% | 4 | 1.47% | 4 | 1.33% |
| Verwijs et al. (2019) | 5 | 0.28% | 5 | 1.54% | 5 | 1.83% | 5 | 1.67% |
| Byng et al. (2016) | 4 | 0.22% | 4 | 1.23% | 4 | 1.47% | 4 | 1.33% |
| Cowan & Lindeman (1989) | 4 | 0.22% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Cuatrecasas (1964) | 4 | 0.22% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Fosberg (1937) | 4 | 0.22% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Lorence & Butaud (2011) | 4 | 0.22% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Moraes (2012) | 4 | 0.22% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Riley (1926) | 4 | 0.22% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Smedmark & Anderberg (2007) | 4 | 0.22% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Yang et al. (2022) | 4 | 0.22% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Butaud & Hodel (2017) | 3 | 0.17% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Butaud et al. (2019) | 3 | 0.17% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Butaud et al. (2023) | 3 | 0.17% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Candolle (1857) | 3 | 0.17% | 3 | 0.92% | 3 | 1.1% | 0 | 0% |
| Ferlay et al. (2023) | 3 | 0.17% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Gagnon et al. (2016) | 3 | 0.17% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Hodel et al. (2021) | 3 | 0.17% | 3 | 0.92% | 3 | 1.1% | 3 | 1% |
| Linnaeus (1753) | 3 | 0.17% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Nepal & Purintun (2021) | 3 | 0.17% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Aurore et al. (2014) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bossa‐Castro et al. (2024) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Couté & Garrouste (2009) | 2 | 0.11% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Frodin (1990) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Gardner et al. (2021) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Gargominy et al. (1996) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Hendrian & Kondo (2007) | 2 | 0.11% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Hodel (2007) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Houlès et al. (2022) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Jost et al. (2019) | 2 | 0.11% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Ollitrault et al. (2020) | 2 | 0.11% | 1 | 0.31% | 0 | 0% | 1 | 0.33% |
| Peraza et al. (2022) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Rohde et al. (2017) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rollet et al. (2010) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Rudd (1965) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Salisbury (1796) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seigler et al. (2014) | 2 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Song et al. (2019) | 2 | 0.11% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Swenson et al. (2023) | 2 | 0.11% | 2 | 0.62% | 2 | 0.73% | 2 | 0.67% |
| Vargas et al. (2024) | 2 | 0.11% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Allorge-Boiteau (2015) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Béreau (2017) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berg (1972) | 1 | 0.06% | 1 | 0.31% | 0 | 0% | 1 | 0.33% |
| Blume (1856) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Boggan et al. (1997) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosser & Heine (2000) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Bovini (2010) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1897) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butaud & Jacq (2013) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Candolle (1815) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1845) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carlquist & Grant (1963) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Colli-Silva et al. (2024) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Don (1831) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forster (1786) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Fosberg & Sachet (1975) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Fournier (1934-1940) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frost et al. (2021) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Gentry (1980) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Gombauld & Duranton (1996) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Guillaumin (1936) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kaastra (1982) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuntze (1891) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1799) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Landrum (1986) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1763) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lobreau-callen (1975) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowry & Plunkett (2010) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Lowry & Plunkett (2020) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Maas & Westra (1992) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marais (1997) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Markgraf (1934) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Maxwell & Veldkamp (1990) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Mazine et al. (2018) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Meyer et al. (2008) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Moench (1794) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mori et al. (2002) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Mouly & Butaud (2023) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Muller et al. (2004) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Nadeaud (1873) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Nyman (1882) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Peck et al. (2014) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Persoon (1807) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prance et al. (2007) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Puttock (1999) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Rabasse et al. (2005) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1792) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robyns (1963) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Rudge (1805) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sachet (1962) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Sagot (1881) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Sant (2022) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Soubeyran (2008) | 1 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson (1991) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Tassin et al. (2006) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Toutain (1989) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 0 | 0% |
| Turner & Veldkamp (2009) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Terebinthaceae"(Anacardiaceae and Burseraceae). Frontiers in Genetics, 5(409): 1-20.">Weeks et al. (2014) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
| Zakardjian et al. (2020) | 1 | 0.06% | 1 | 0.31% | 1 | 0.37% | 1 | 0.33% |
