Arbres de Nouvelle-Calédonie
146 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 | 47,18% | 532 | 71,03% | 408 | 66,67% | 528 | 76,52% |
Morat et al. (2012) | 734 | 30,01% | 564 | 75,3% | 446 | 72,88% | 511 | 74,06% |
Véron et al. (2021) | 524 | 21,42% | 519 | 69,29% | 405 | 66,18% | 478 | 69,28% |
Fournet (2002) | 496 | 20,28% | 456 | 60,88% | 456 | 74,51% | 436 | 63,19% |
Anonyme (2014) | 347 | 14,19% | 303 | 40,45% | 303 | 49,51% | 286 | 41,45% |
Molino et al. (2022) | 329 | 13,45% | 22 | 2,94% | 22 | 3,59% | 22 | 3,19% |
Hequet & Le Corre (2010) | 143 | 5,85% | 124 | 16,56% | 122 | 19,93% | 122 | 17,68% |
Hequet et al. (2009) | 143 | 5,85% | 124 | 16,56% | 122 | 19,93% | 122 | 17,68% |
MacKee (1994) | 143 | 5,85% | 123 | 16,42% | 121 | 19,77% | 121 | 17,54% |
Funk et al. (2007) | 135 | 5,52% | 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 | 2,62% | 59 | 7,88% | 56 | 9,15% | 57 | 8,26% |
Fourdrigniez & Meyer (2008) | 63 | 2,58% | 58 | 7,74% | 56 | 9,15% | 54 | 7,83% |
Tison et al. (2014) | 53 | 2,17% | 39 | 5,21% | 39 | 6,37% | 35 | 5,07% |
Morat & Veillon (1985) | 51 | 2,09% | 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 | 0,7% | 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% |
Linnaeus (1753) | 11 | 0,45% | 8 | 1,07% | 7 | 1,14% | 7 | 1,01% |
Miller (1768) | 10 | 0,41% | 2 | 0,27% | 2 | 0,33% | 2 | 0,29% |
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% |
Meyer et al. (2006) | 9 | 0,37% | 6 | 0,8% | 5 | 0,82% | 6 | 0,87% |
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 | 0,25% | 6 | 0,8% | 6 | 0,98% | 6 | 0,87% |
Hendrian & Kondo (2007) | 6 | 0,25% | 3 | 0,4% | 3 | 0,49% | 3 | 0,43% |
Lavergne (2011) | 6 | 0,25% | 5 | 0,67% | 5 | 0,82% | 4 | 0,58% |
Pennington & Biggs (2016) | 6 | 0,25% | 5 | 0,67% | 5 | 0,82% | 5 | 0,72% |
Salisbury (1796) | 6 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Schatz & Lowry (2018) | 6 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Verwijs et al. (2019) | 6 | 0,25% | 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% |
Maas et al. (2023) | 5 | 0,2% | 4 | 0,53% | 4 | 0,65% | 4 | 0,58% |
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% |
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% |
Bossa‐Castro et al. (2024) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
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% |
Colli-Silva et al. (2024) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
Don (1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 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% |
Pearman et al. (2020) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
Peck et al. (2014) | 1 | 0,04% | 1 | 0,13% | 1 | 0,16% | 1 | 0,14% |
Persoon (1807) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |