Arbres de Saint-Martin
112 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) | 533 | 42.03% | 24 | 17.39% | 24 | 18.18% | 21 | 15.91% |
Fournet (2002) | 476 | 37.54% | 412 | 298.55% | 412 | 312.12% | 396 | 300% |
Funk et al. (2007) | 183 | 14.43% | 61 | 44.2% | 61 | 46.21% | 57 | 43.18% |
Molino et al. (2009) | 45 | 3.55% | 41 | 29.71% | 41 | 31.06% | 38 | 28.79% |
Hequet & Le Corre (2010) | 44 | 3.47% | 39 | 28.26% | 39 | 29.55% | 39 | 29.55% |
Hequet et al. (2009) | 44 | 3.47% | 39 | 28.26% | 39 | 29.55% | 39 | 29.55% |
MacKee (1994) | 44 | 3.47% | 39 | 28.26% | 39 | 29.55% | 39 | 29.55% |
Méndez (2001) | 33 | 2.6% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Ter Steege et al. (2016) | 31 | 2.44% | 30 | 21.74% | 30 | 22.73% | 27 | 20.45% |
Acevedo-Rodríguez & Strong (2012) | 29 | 2.29% | 22 | 15.94% | 18 | 13.64% | 22 | 16.67% |
Delnatte & Meyer (2012) | 29 | 2.29% | 26 | 18.84% | 26 | 19.7% | 26 | 19.7% |
Stace (2010) | 26 | 2.05% | 9 | 6.52% | 5 | 3.79% | 7 | 5.3% |
Fourdrigniez & Meyer (2008) | 25 | 1.97% | 24 | 17.39% | 24 | 18.18% | 23 | 17.42% |
Anonyme (2014) | 22 | 1.74% | 19 | 13.77% | 19 | 14.39% | 18 | 13.64% |
Ståhl (2010) | 22 | 1.74% | 6 | 4.35% | 6 | 4.55% | 6 | 4.55% |
Aublet (1775) | 21 | 1.66% | 7 | 5.07% | 7 | 5.3% | 7 | 5.3% |
Cornejo (2020) | 20 | 1.58% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Boullet et al. (2018) | 14 | 1.1% | 13 | 9.42% | 13 | 9.85% | 12 | 9.09% |
Fryxell (2001) | 14 | 1.1% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
D'arcy (1987) | 13 | 1.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat & Veillon (1985) | 13 | 1.03% | 9 | 6.52% | 9 | 6.82% | 8 | 6.06% |
O'leary et al. (2021) | 12 | 0.95% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Morat et al. (2012) | 11 | 0.87% | 6 | 4.35% | 5 | 3.79% | 5 | 3.79% |
Munzinger et al. (2016) | 10 | 0.79% | 4 | 2.9% | 3 | 2.27% | 4 | 3.03% |
Lemée (1952) | 9 | 0.71% | 6 | 4.35% | 6 | 4.55% | 6 | 4.55% |
Tison et al. (2014) | 8 | 0.63% | 5 | 3.62% | 5 | 3.79% | 3 | 2.27% |
Berg & Roselli (2005) | 7 | 0.55% | 6 | 4.35% | 3 | 2.27% | 3 | 2.27% |
Florence (2004) | 7 | 0.55% | 7 | 5.07% | 7 | 5.3% | 7 | 5.3% |
Zerega et al. (2005) | 7 | 0.55% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Bovini (2010) | 6 | 0.47% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Miller (1768) | 6 | 0.47% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Allen et al. (2022) | 5 | 0.39% | 5 | 3.62% | 5 | 3.79% | 5 | 3.79% |
Berg (1992) | 5 | 0.39% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Cornejo & Iltis (2007) | 5 | 0.39% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Cremers & Hoff (1997) | 5 | 0.39% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez (2012) | 4 | 0.32% | 2 | 1.45% | 2 | 1.52% | 1 | 0.76% |
Cowan & Lindeman (1989) | 4 | 0.32% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Feuillet (2020) | 4 | 0.32% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Granville & Gayot (2014) | 4 | 0.32% | 4 | 2.9% | 4 | 3.03% | 4 | 3.03% |
Hauenschild et al. (2016) | 4 | 0.32% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Lavergne (2011) | 4 | 0.32% | 4 | 2.9% | 4 | 3.03% | 4 | 3.03% |
Léotard & Chaline (2013) | 4 | 0.32% | 4 | 2.9% | 4 | 3.03% | 4 | 3.03% |
Mazine et al. (2018) | 4 | 0.32% | 4 | 2.9% | 4 | 3.03% | 4 | 3.03% |
Véron et al. (2021) | 4 | 0.32% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Fritsch (2003) | 3 | 0.24% | 3 | 2.17% | 3 | 2.27% | 3 | 2.27% |
Gagnon et al. (2016) | 3 | 0.24% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Linnaeus (1753) | 3 | 0.24% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Linnaeus (1753) | 3 | 0.24% | 3 | 2.17% | 2 | 1.52% | 2 | 1.52% |
Meyer et al. (2006) | 3 | 0.24% | 3 | 2.17% | 3 | 2.27% | 3 | 2.27% |
Allorge-Boiteau (2015) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Arriagada (2003) | 2 | 0.16% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Aurore et al. (2014) | 2 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1992) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Campbell et al. (2019) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Couté & Garrouste (2009) | 2 | 0.16% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
David & Thiebaut (2013) | 2 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Duss (1897) | 2 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1997) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Gentry (1980) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Jost et al. (2019) | 2 | 0.16% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Kyalangalilwa et al. (2013) | 2 | 0.16% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Lemée (1955) | 2 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas et al. (2023) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Mestier et al. (2022) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Mitchell (1997) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Ollitrault et al. (2020) | 2 | 0.16% | 1 | 0.72% | 0 | 0% | 1 | 0.76% |
Paudyal et al. (2018) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Peraza et al. (2022) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Prado et al. (2013) | 2 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2012) | 2 | 0.16% | 2 | 1.45% | 2 | 1.52% | 2 | 1.52% |
Béreau (2017) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1997) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Bos et al. (2018) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Bosser & Heine (2000) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Bouman et al. (2020) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Bouman et al. (2022) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Byng et al. (2016) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Candolle (1845) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Delprete & Kirkbride (2015) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Don (1831) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Frost et al. (2021) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Gardner et al. (2021) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Gargominy et al. (1996) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Gombauld & Duranton (1996) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Greuter & Rankin‐Rodríguez (2021) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Grose & Olmstead (2007) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Guillaumin (1936) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrington & Gadek (2009) | 1 | 0.08% | 1 | 0.72% | 0 | 0% | 1 | 0.76% |
Harrington (2008) | 1 | 0.08% | 1 | 0.72% | 0 | 0% | 1 | 0.76% |
Kaastra (1982) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Landrum (1986) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Manzitto‐Tripp et al. (2021) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Meyer et al. (2008) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Moench (1794) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1933) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Mori et al. (2002) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Peck et al. (2014) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Pennington & Biggs (2016) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Pennington (1990) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Persoon (1807) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Sagot (1881) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Samarakoon (2015) | 1 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Song et al. (2019) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Taylor et al. (2017) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Trofimov et al. (2016) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Webster (1958) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Yuan et al. (2010) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |
Zakardjian et al. (2020) | 1 | 0.08% | 1 | 0.72% | 1 | 0.76% | 1 | 0.76% |