Arbres de Nouvelle-Calédonie
141 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Munzinger et al. (2016) | 1154 | 47,12% | 532 | 71,03% | 408 | 66,67% | 528 | 76,52% |
| Morat et al. (2012) | 734 | 29,97% | 564 | 75,3% | 446 | 72,88% | 511 | 74,06% |
| Véron et al. (2021) | 524 | 21,4% | 519 | 69,29% | 405 | 66,18% | 478 | 69,28% |
| Fournet (2002) | 500 | 20,42% | 456 | 60,88% | 456 | 74,51% | 436 | 63,19% |
| Anonyme (2014) | 347 | 14,17% | 303 | 40,45% | 303 | 49,51% | 286 | 41,45% |
| Molino et al. (2022) | 329 | 13,43% | 22 | 2,94% | 22 | 3,59% | 22 | 3,19% |
| Hequet & Le Corre (2010) | 144 | 5,88% | 124 | 16,56% | 122 | 19,93% | 122 | 17,68% |
| Hequet et al. (2009) | 144 | 5,88% | 124 | 16,56% | 122 | 19,93% | 122 | 17,68% |
| MacKee (1994) | 144 | 5,88% | 123 | 16,42% | 121 | 19,77% | 121 | 17,54% |
| Funk et al. (2007) | 135 | 5,51% | 69 | 9,21% | 68 | 11,11% | 65 | 9,42% |
| Delnatte & Meyer (2012) | 68 | 2,78% | 59 | 7,88% | 59 | 9,64% | 57 | 8,26% |
| Molino et al. (2009) | 68 | 2,78% | 62 | 8,28% | 62 | 10,13% | 60 | 8,7% |
| Couhia & Fleurot (2016) | 64 | 2,61% | 59 | 7,88% | 56 | 9,15% | 57 | 8,26% |
| Fourdrigniez & Meyer (2008) | 63 | 2,57% | 58 | 7,74% | 56 | 9,15% | 54 | 7,83% |
| Tison et al. (2014) | 53 | 2,16% | 37 | 4,94% | 37 | 6,05% | 35 | 5,07% |
| Morat & Veillon (1985) | 51 | 2,08% | 42 | 5,61% | 42 | 6,86% | 38 | 5,51% |
| Boullet et al. (2018) | 33 | 1,35% | 32 | 4,27% | 32 | 5,23% | 29 | 4,2% |
| Ter Steege et al. (2016) | 32 | 1,31% | 31 | 4,14% | 31 | 5,07% | 31 | 4,49% |
| Mitchell & Daly (2015) | 26 | 1,06% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Acevedo-Rodríguez & Strong (2012) | 25 | 1,02% | 23 | 3,07% | 20 | 3,27% | 18 | 2,61% |
| Aublet (1775) | 21 | 0,86% | 8 | 1,07% | 8 | 1,31% | 8 | 1,16% |
| Florence (2004) | 20 | 0,82% | 18 | 2,4% | 17 | 2,78% | 18 | 2,61% |
| Hopkins et al. (2014) | 17 | 0,69% | 17 | 2,27% | 15 | 2,45% | 16 | 2,32% |
| Florence (1997) | 16 | 0,65% | 16 | 2,14% | 15 | 2,45% | 16 | 2,32% |
| Barneby & Grimes (1996) | 13 | 0,53% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Berg & Roselli (2005) | 13 | 0,53% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Hodel & Pintaud (2021) | 12 | 0,49% | 12 | 1,6% | 0 | 0% | 12 | 1,74% |
| Léotard & Chaline (2013) | 12 | 0,49% | 12 | 1,6% | 12 | 1,96% | 11 | 1,59% |
| Allen et al. (2022) | 9 | 0,37% | 9 | 1,2% | 9 | 1,47% | 8 | 1,16% |
| Berg (1992) | 9 | 0,37% | 4 | 0,53% | 4 | 0,65% | 4 | 0,58% |
| Kyalangalilwa et al. (2013) | 9 | 0,37% | 3 | 0,4% | 2 | 0,33% | 2 | 0,29% |
| Linnaeus (1753) | 9 | 0,37% | 6 | 0,8% | 6 | 0,98% | 6 | 0,87% |
| Meyer et al. (2006) | 9 | 0,37% | 6 | 0,8% | 5 | 0,82% | 6 | 0,87% |
| Miller (1768) | 9 | 0,37% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Mitchell (1997) | 9 | 0,37% | 5 | 0,67% | 5 | 0,82% | 5 | 0,72% |
| Pennington (1990) | 9 | 0,37% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Stace (2010) | 9 | 0,37% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Lemée (1952) | 7 | 0,29% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Zerega et al. (2005) | 7 | 0,29% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Buerki et al. (2020) | 6 | 0,24% | 6 | 0,8% | 6 | 0,98% | 6 | 0,87% |
| Hendrian & Kondo (2007) | 6 | 0,24% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Lavergne (2011) | 6 | 0,24% | 5 | 0,67% | 5 | 0,82% | 4 | 0,58% |
| Pennington & Biggs (2016) | 6 | 0,24% | 5 | 0,67% | 5 | 0,82% | 5 | 0,72% |
| Salisbury (1796) | 6 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schatz & Lowry (2018) | 6 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verwijs et al. (2019) | 6 | 0,24% | 6 | 0,8% | 3 | 0,49% | 5 | 0,72% |
| Acevedo-Rodríguez (2012) | 5 | 0,2% | 3 | 0,4% | 3 | 0,49% | 2 | 0,29% |
| Granville & Gayot (2014) | 5 | 0,2% | 5 | 0,67% | 5 | 0,82% | 5 | 0,72% |
| Hodel et al. (2021) | 5 | 0,2% | 5 | 0,67% | 5 | 0,82% | 4 | 0,58% |
| Lowe et al. (2007) | 5 | 0,2% | 5 | 0,67% | 5 | 0,82% | 5 | 0,72% |
| Byng et al. (2016) | 4 | 0,16% | 4 | 0,53% | 4 | 0,65% | 4 | 0,58% |
| Cowan & Lindeman (1989) | 4 | 0,16% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Cuatrecasas (1964) | 4 | 0,16% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Ferlay et al. (2023) | 4 | 0,16% | 4 | 0,53% | 4 | 0,65% | 4 | 0,58% |
| Fryxell (2001) | 4 | 0,16% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Gardner et al. (2021) | 4 | 0,16% | 4 | 0,53% | 4 | 0,65% | 3 | 0,43% |
| Linnaeus (1753) | 4 | 0,16% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Samuel et al. (2019) | 4 | 0,16% | 4 | 0,53% | 4 | 0,65% | 4 | 0,58% |
| Yang et al. (2022) | 4 | 0,16% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Gâteblé et al. (2018) | 3 | 0,12% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
| Loesener (1901) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Song et al. (2019) | 3 | 0,12% | 2 | 0,27% | 2 | 0,33% | 1 | 0,14% |
| Souza et al. (2022) | 3 | 0,12% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Allorge-Boiteau (2015) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Aurore et al. (2014) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couté & Garrouste (2009) | 2 | 0,08% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Cremers & Hoff (1998) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fosberg (1937) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardner et al. (2021) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Gargominy et al. (1996) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Harrington & Gadek (2009) | 2 | 0,08% | 2 | 0,27% | 0 | 0% | 2 | 0,29% |
| Harrington (2008) | 2 | 0,08% | 2 | 0,27% | 0 | 0% | 2 | 0,29% |
| Houlès et al. (2022) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 0 | 0% |
| Jost et al. (2019) | 2 | 0,08% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Kuntze (1891) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moore (1933) | 2 | 0,08% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Mori et al. (2002) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Ollitrault et al. (2020) | 2 | 0,08% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
| Peraza et al. (2022) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Richard (1792) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rohde et al. (2017) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1913) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seigler et al. (2014) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Swenson et al. (2023) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Tassin et al. (2006) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Wells et al. (2021) | 2 | 0,08% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
| Appelhans et al. (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béguinot (2012) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Béreau (2017) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berg (1972) | 1 | 0,04% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
| Boggan et al. (1992) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boggan et al. (1997) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosser & Heine (2000) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Bouman et al. (2020) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Bouman et al. (2022) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Bovini (2010) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boyd et al. (2006) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1897) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butaud (2015) | 1 | 0,04% | 1 | 0,13% | 0 | 0% | 1 | 0,14% |
| Candolle (1815) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1845) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Don (1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gentry (1980) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Gray (1821) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grose & Olmstead (2007) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Guillaumin (1936) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hollowell et al. (2001) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hopkins & Pillon (2019) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Kaastra (1982) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krebs et al. (2004) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Lamarck (1783) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1798) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Landrum (1986) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemée (1953) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1763) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lobreau-callen (1975) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowry & Plunkett (2020) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Marais (1997) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Mazine et al. (2018) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Méndez Santos (2001) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Meyer et al. (2008) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Moench (1794) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Munzinger et al. (2021) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Munzinger et al. (2023) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Nyman (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peck et al. (2014) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Prance et al. (2007) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Rabasse et al. (2005) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rivière (2003) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Sachet (1962) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Sagot (1881) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Scopoli (1771) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soares et al. (2021) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Soubeyran (2008) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson (1991) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 0 | 0% |
| Toutain (1989) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Villanueva-almanza et al. (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Webster (1956) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Webster (1957) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
| Zakardjian et al. (2020) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
