Arbres de Polynésie française
153 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) | 502 | 27,94% | 30 | 9,23% | 30 | 10,99% | 29 | 9,67% |
| Fournet (2002) | 472 | 26,27% | 420 | 129,23% | 420 | 153,85% | 384 | 128% |
| Funk et al. (2007) | 181 | 10,07% | 71 | 21,85% | 69 | 25,27% | 66 | 22% |
| Munzinger et al. (2016) | 151 | 8,4% | 41 | 12,62% | 39 | 14,29% | 36 | 12% |
| Anonyme (2014) | 125 | 6,96% | 107 | 32,92% | 107 | 39,19% | 94 | 31,33% |
| Hequet & Le Corre (2010) | 125 | 6,96% | 107 | 32,92% | 106 | 38,83% | 98 | 32,67% |
| Hequet et al. (2009) | 125 | 6,96% | 107 | 32,92% | 106 | 38,83% | 98 | 32,67% |
| MacKee (1994) | 125 | 6,96% | 106 | 32,62% | 105 | 38,46% | 98 | 32,67% |
| Véron et al. (2021) | 90 | 5,01% | 86 | 26,46% | 67 | 24,54% | 82 | 27,33% |
| Molino et al. (2009) | 74 | 4,12% | 66 | 20,31% | 66 | 24,18% | 63 | 21% |
| Fourdrigniez & Meyer (2008) | 73 | 4,06% | 67 | 20,62% | 62 | 22,71% | 61 | 20,33% |
| Morat et al. (2012) | 72 | 4,01% | 44 | 13,54% | 43 | 15,75% | 38 | 12,67% |
| Delnatte & Meyer (2012) | 62 | 3,45% | 54 | 16,62% | 54 | 19,78% | 48 | 16% |
| Florence (1997) | 61 | 3,39% | 61 | 18,77% | 56 | 20,51% | 60 | 20% |
| Morat & Veillon (1985) | 55 | 3,06% | 46 | 14,15% | 46 | 16,85% | 39 | 13% |
| Tison et al. (2014) | 42 | 2,34% | 31 | 9,54% | 31 | 11,36% | 27 | 9% |
| Ter Steege et al. (2016) | 38 | 2,11% | 35 | 10,77% | 35 | 12,82% | 34 | 11,33% |
| Florence (2004) | 36 | 2% | 28 | 8,62% | 24 | 8,79% | 28 | 9,33% |
| Boullet et al. (2018) | 32 | 1,78% | 31 | 9,54% | 31 | 11,36% | 30 | 10% |
| Acevedo-Rodríguez & Strong (2012) | 26 | 1,45% | 22 | 6,77% | 22 | 8,06% | 13 | 4,33% |
| Aublet (1775) | 20 | 1,11% | 9 | 2,77% | 9 | 3,3% | 9 | 3% |
| Mitchell & Daly (2015) | 18 | 1% | 2 | 0,62% | 2 | 0,73% | 2 | 0,67% |
| Florence (1996) | 16 | 0,89% | 16 | 4,92% | 16 | 5,86% | 16 | 5,33% |
| Berg & Roselli (2005) | 13 | 0,72% | 1 | 0,31% | 1 | 0,37% | 1 | 0,33% |
| Brandbyge (1986) | 13 | 0,72% | 1 | 0,31% | 1 | 0,37% | 1 | 0,33% |
| Moore (1933) | 13 | 0,72% | 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 | 0,61% | 11 | 3,38% | 10 | 3,66% | 9 | 3% |
| Couhia & Fleurot (2016) | 11 | 0,61% | 11 | 3,38% | 11 | 4,03% | 9 | 3% |
| Léotard & Chaline (2013) | 11 | 0,61% | 11 | 3,38% | 11 | 4,03% | 9 | 3% |
| Maas et al. (2023) | 10 | 0,56% | 5 | 1,54% | 5 | 1,83% | 5 | 1,67% |
| Miller (1768) | 10 | 0,56% | 2 | 0,62% | 2 | 0,73% | 2 | 0,67% |
| Kyalangalilwa et al. (2013) | 9 | 0,5% | 3 | 0,92% | 2 | 0,73% | 2 | 0,67% |
| Meyer et al. (2006) | 9 | 0,5% | 6 | 1,85% | 5 | 1,83% | 6 | 2% |
| Pennington (1990) | 9 | 0,5% | 3 | 0,92% | 3 | 1,1% | 3 | 1% |
| Stace (2010) | 9 | 0,5% | 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% |
| 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 | 0,33% | 4 | 1,23% | 4 | 1,47% | 4 | 1,33% |
| Fosberg & Sachet (1981) | 6 | 0,33% | 6 | 1,85% | 0 | 0% | 6 | 2% |
| Mitchell (1997) | 6 | 0,33% | 4 | 1,23% | 4 | 1,47% | 4 | 1,33% |
| Moore (1940) | 6 | 0,33% | 3 | 0,92% | 3 | 1,1% | 3 | 1% |
| Rainer (2007) | 6 | 0,33% | 1 | 0,31% | 1 | 0,37% | 1 | 0,33% |
| Sleumer (1938) | 6 | 0,33% | 4 | 1,23% | 0 | 0% | 4 | 1,33% |
| Berg (1992) | 5 | 0,28% | 3 | 0,92% | 3 | 1,1% | 3 | 1% |
| Granville & Gayot (2014) | 5 | 0,28% | 5 | 1,54% | 5 | 1,83% | 5 | 1,67% |
| 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% |
| 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% |
| Gentry (1980) | 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% |
| Méndez Santos (2001) | 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% |
