Arbres de Saint-Martin
107 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 | 41,84% | 24 | 17,39% | 24 | 18,18% | 21 | 15,91% |
| Fournet (2002) | 480 | 37,68% | 412 | 298,55% | 412 | 312,12% | 396 | 300% |
| Funk et al. (2007) | 183 | 14,36% | 61 | 44,2% | 61 | 46,21% | 57 | 43,18% |
| Hequet & Le Corre (2010) | 45 | 3,53% | 39 | 28,26% | 39 | 29,55% | 39 | 29,55% |
| Hequet et al. (2009) | 45 | 3,53% | 39 | 28,26% | 39 | 29,55% | 39 | 29,55% |
| MacKee (1994) | 45 | 3,53% | 39 | 28,26% | 39 | 29,55% | 39 | 29,55% |
| Molino et al. (2009) | 45 | 3,53% | 41 | 29,71% | 41 | 31,06% | 38 | 28,79% |
| Ter Steege et al. (2016) | 31 | 2,43% | 30 | 21,74% | 30 | 22,73% | 27 | 20,45% |
| Acevedo-Rodríguez & Strong (2012) | 29 | 2,28% | 22 | 15,94% | 18 | 13,64% | 22 | 16,67% |
| Delnatte & Meyer (2012) | 29 | 2,28% | 26 | 18,84% | 26 | 19,7% | 26 | 19,7% |
| Stace (2010) | 26 | 2,04% | 9 | 6,52% | 5 | 3,79% | 7 | 5,3% |
| Fourdrigniez & Meyer (2008) | 25 | 1,96% | 24 | 17,39% | 24 | 18,18% | 23 | 17,42% |
| Anonyme (2014) | 22 | 1,73% | 19 | 13,77% | 19 | 14,39% | 18 | 13,64% |
| Ståhl (2010) | 22 | 1,73% | 6 | 4,35% | 6 | 4,55% | 6 | 4,55% |
| Aublet (1775) | 20 | 1,57% | 7 | 5,07% | 7 | 5,3% | 7 | 5,3% |
| Cornejo (2020) | 20 | 1,57% | 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 | 1,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat & Veillon (1985) | 13 | 1,02% | 9 | 6,52% | 9 | 6,82% | 8 | 6,06% |
| Morat et al. (2012) | 11 | 0,86% | 6 | 4,35% | 5 | 3,79% | 5 | 3,79% |
| Munzinger et al. (2016) | 10 | 0,78% | 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% | 3 | 2,17% | 3 | 2,27% | 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% |
| 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% |
| Miller (1768) | 5 | 0,39% | 1 | 0,72% | 1 | 0,76% | 1 | 0,76% |
| Acevedo-Rodríguez (2012) | 4 | 0,31% | 2 | 1,45% | 2 | 1,52% | 1 | 0,76% |
| Cowan & Lindeman (1989) | 4 | 0,31% | 1 | 0,72% | 1 | 0,76% | 1 | 0,76% |
| Feuillet (2020) | 4 | 0,31% | 2 | 1,45% | 2 | 1,52% | 2 | 1,52% |
| Hauenschild et al. (2016) | 4 | 0,31% | 1 | 0,72% | 1 | 0,76% | 1 | 0,76% |
| Lavergne (2011) | 4 | 0,31% | 4 | 2,9% | 4 | 3,03% | 4 | 3,03% |
| Léotard & Chaline (2013) | 4 | 0,31% | 4 | 2,9% | 4 | 3,03% | 4 | 3,03% |
| Mazine et al. (2018) | 4 | 0,31% | 4 | 2,9% | 4 | 3,03% | 4 | 3,03% |
| Véron et al. (2021) | 4 | 0,31% | 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% |
| 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% |
| Granville & Gayot (2014) | 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% |
| 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% |
| Appelhans et al. (2021) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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% |
| 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% |
| 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 (1753) | 1 | 0,08% | 1 | 0,72% | 1 | 0,76% | 1 | 0,76% |
| 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% |
| Méndez Santos (2001) | 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% |
| 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% |
