Arbres de la Guadeloupe
215 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fournet (2002) | 1887 | 46,1% | 1574 | 294,76% | 1570 | 314% | 1518 | 301,19% |
Molino et al. (2022) | 1644 | 40,17% | 96 | 17,98% | 92 | 18,4% | 91 | 18,06% |
Funk et al. (2007) | 644 | 15,73% | 195 | 36,52% | 189 | 37,8% | 177 | 35,12% |
Véron et al. (2021) | 149 | 3,64% | 138 | 25,84% | 126 | 25,2% | 137 | 27,18% |
Molino et al. (2009) | 142 | 3,47% | 124 | 23,22% | 124 | 24,8% | 114 | 22,62% |
Acevedo-Rodríguez & Strong (2012) | 127 | 3,1% | 95 | 17,79% | 82 | 16,4% | 89 | 17,66% |
Ter Steege et al. (2016) | 126 | 3,08% | 113 | 21,16% | 113 | 22,6% | 101 | 20,04% |
Hequet & Le Corre (2010) | 118 | 2,88% | 101 | 18,91% | 101 | 20,2% | 98 | 19,44% |
Hequet et al. (2009) | 118 | 2,88% | 101 | 18,91% | 101 | 20,2% | 98 | 19,44% |
MacKee (1994) | 118 | 2,88% | 100 | 18,73% | 100 | 20% | 97 | 19,25% |
Munzinger et al. (2016) | 82 | 2% | 20 | 3,75% | 19 | 3,8% | 19 | 3,77% |
Anonyme (2014) | 77 | 1,88% | 66 | 12,36% | 66 | 13,2% | 64 | 12,7% |
Delnatte & Meyer (2012) | 71 | 1,73% | 59 | 11,05% | 59 | 11,8% | 57 | 11,31% |
Pennington (1990) | 70 | 1,71% | 20 | 3,75% | 10 | 2% | 14 | 2,78% |
Fourdrigniez & Meyer (2008) | 58 | 1,42% | 53 | 9,93% | 52 | 10,4% | 51 | 10,12% |
Stace (2010) | 49 | 1,2% | 12 | 2,25% | 8 | 1,6% | 10 | 1,98% |
Aublet (1775) | 39 | 0,95% | 16 | 3% | 16 | 3,2% | 16 | 3,17% |
Tison et al. (2014) | 33 | 0,81% | 24 | 4,49% | 24 | 4,8% | 22 | 4,37% |
Morat et al. (2012) | 32 | 0,78% | 22 | 4,12% | 21 | 4,2% | 20 | 3,97% |
Barneby & Grimes (1996) | 31 | 0,76% | 1 | 0,19% | 1 | 0,2% | 0 | 0% |
Morat & Veillon (1985) | 31 | 0,76% | 26 | 4,87% | 26 | 5,2% | 24 | 4,76% |
Penneys & Judd (2005) | 30 | 0,73% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Cornejo (2020) | 28 | 0,68% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Mitchell & Daly (2015) | 26 | 0,64% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Boullet et al. (2018) | 25 | 0,61% | 24 | 4,49% | 24 | 4,8% | 23 | 4,56% |
Ståhl (2010) | 24 | 0,59% | 7 | 1,31% | 7 | 1,4% | 7 | 1,39% |
Lemée (1952) | 20 | 0,49% | 13 | 2,43% | 13 | 2,6% | 13 | 2,58% |
Kriebel (2016) | 19 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Pennington & Biggs (2016) | 19 | 0,46% | 12 | 2,25% | 11 | 2,2% | 10 | 1,98% |
Florence (2004) | 18 | 0,44% | 16 | 3% | 16 | 3,2% | 16 | 3,17% |
Soares et al. (2021) | 16 | 0,39% | 5 | 0,94% | 4 | 0,8% | 2 | 0,4% |
Webster (2003) | 16 | 0,39% | 7 | 1,31% | 4 | 0,8% | 6 | 1,19% |
Berg (1992) | 14 | 0,34% | 5 | 0,94% | 5 | 1% | 5 | 0,99% |
Fryxell (2001) | 14 | 0,34% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
D'arcy (1987) | 13 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Görts-van Rijn (2007) | 13 | 0,32% | 3 | 0,56% | 3 | 0,6% | 2 | 0,4% |
Michelangeli et al. (2018) | 13 | 0,32% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Léotard & Chaline (2013) | 12 | 0,29% | 12 | 2,25% | 12 | 2,4% | 12 | 2,38% |
Maas et al. (2023) | 12 | 0,29% | 6 | 1,12% | 6 | 1,2% | 6 | 1,19% |
Daly & Fine (2018) | 11 | 0,27% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Florence (1997) | 11 | 0,27% | 11 | 2,06% | 10 | 2% | 11 | 2,18% |
Acevedo-Rodríguez (2012) | 10 | 0,24% | 6 | 1,12% | 6 | 1,2% | 5 | 0,99% |
Azevedo Tozzi & Silva (2007) | 10 | 0,24% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Judd et al. (2018) | 10 | 0,24% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Mitchell (1997) | 9 | 0,22% | 5 | 0,94% | 5 | 1% | 5 | 0,99% |
Biral et al. (2017) | 8 | 0,2% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Kyalangalilwa et al. (2013) | 8 | 0,2% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Linnaeus (1753) | 8 | 0,2% | 6 | 1,12% | 5 | 1% | 5 | 0,99% |
Miller (1768) | 8 | 0,2% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Allen et al. (2022) | 7 | 0,17% | 7 | 1,31% | 7 | 1,4% | 7 | 1,39% |
Berg & Roselli (2005) | 7 | 0,17% | 6 | 1,12% | 3 | 0,6% | 3 | 0,6% |
Granville & Gayot (2014) | 7 | 0,17% | 7 | 1,31% | 7 | 1,4% | 6 | 1,19% |
Mazine et al. (2018) | 7 | 0,17% | 6 | 1,12% | 6 | 1,2% | 5 | 0,99% |
Meyer et al. (2006) | 7 | 0,17% | 5 | 0,94% | 5 | 1% | 5 | 0,99% |
Rohde et al. (2017) | 7 | 0,17% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Swenson et al. (2023) | 7 | 0,17% | 7 | 1,31% | 7 | 1,4% | 5 | 0,99% |
Zerega et al. (2005) | 7 | 0,17% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Boggan et al. (1992) | 6 | 0,15% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Bovini (2010) | 6 | 0,15% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Chanderbali (2004) | 6 | 0,15% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Fiaschi et al. (2020) | 6 | 0,15% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Paudyal et al. (2018) | 6 | 0,15% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Pennington & Clarkson (2013) | 6 | 0,15% | 2 | 0,37% | 0 | 0% | 2 | 0,4% |
Peraza et al. (2022) | 6 | 0,15% | 5 | 0,94% | 5 | 1% | 5 | 0,99% |
Rainer (2007) | 6 | 0,15% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Bouman et al. (2022) | 5 | 0,12% | 5 | 0,94% | 5 | 1% | 2 | 0,4% |
Christenhusz (2009) | 5 | 0,12% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Cornejo & Iltis (2007) | 5 | 0,12% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Cremers & Hoff (1997) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 5 | 0,12% | 5 | 0,94% | 5 | 1% | 5 | 0,99% |
Lavergne (2011) | 5 | 0,12% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Moraes (2012) | 5 | 0,12% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Bernard (2015) | 4 | 0,1% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Biral (2016) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouman et al. (2020) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 1 | 0,2% |
Byng et al. (2016) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Couhia & Fleurot (2016) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Cowan & Lindeman (1989) | 4 | 0,1% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Cuatrecasas (1964) | 4 | 0,1% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Feuillet (2013) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2020) | 4 | 0,1% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Fritsch & Almeda (2015) | 4 | 0,1% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Gardner et al. (2021) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 3 | 0,6% |
Linnaeus (1753) | 4 | 0,1% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Lowe et al. (2007) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Mori et al. (2002) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Richard (1792) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2022) | 4 | 0,1% | 4 | 0,75% | 4 | 0,8% | 4 | 0,79% |
Webster (1956) | 4 | 0,1% | 3 | 0,56% | 1 | 0,2% | 2 | 0,4% |
Wunderlin (2009) | 4 | 0,1% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Yang et al. (2022) | 4 | 0,1% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Boggan et al. (1997) | 3 | 0,07% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Fritsch (2003) | 3 | 0,07% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Henderson (2011) | 3 | 0,07% | 1 | 0,19% | 1 | 0,2% | 0 | 0% |
Lemée (1953) | 3 | 0,07% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Loesener (1901) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowry et al. (2019) | 3 | 0,07% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Maurin et al. (2017) | 3 | 0,07% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Ollitrault et al. (2020) | 3 | 0,07% | 2 | 0,37% | 0 | 0% | 2 | 0,4% |
Pennington & Wise (2017) | 3 | 0,07% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Rudd (1965) | 3 | 0,07% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Salisbury (1796) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Song et al. (2019) | 3 | 0,07% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Sothers et al. (2016) | 3 | 0,07% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Trofimov et al. (2016) | 3 | 0,07% | 3 | 0,56% | 3 | 0,6% | 3 | 0,6% |
Yesilyurt (2009) | 3 | 0,07% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Allorge-Boiteau (2015) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 1 | 0,2% |
Arriagada (2003) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Aurore et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Béreau (2017) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Biral (2019) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Borchsenius & Bernal (1996) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Bossa‐Castro et al. (2024) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Campbell et al. (2019) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Couté & Garrouste (2009) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Cremers & Hoff (1998) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
David & Thiebaut (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duss (1897) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2009) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Fine et al. (2014) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Gardner et al. (2021) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Gargominy et al. (1996) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Goldenberg et al. (2013) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 0 | 0% |
González-Gutiérrez (2007) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Greuter & Rankin‐Rodríguez (2021) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Grose & Olmstead (2007) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Jost et al. (2019) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Kuntze (1891) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1955) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lourenço et al. (2018) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Prado et al. (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Robyns (1963) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Seigler et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
van der Werff (2020) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Webster (1957) | 2 | 0,05% | 1 | 0,19% | 1 | 0,2% | 0 | 0% |
Wells et al. (2021) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Yang et al. (2012) | 2 | 0,05% | 2 | 0,37% | 2 | 0,4% | 2 | 0,4% |
Alverson (1989) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Appelhans et al. (2021) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Barneby et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barthelat (2019) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Berg (1972) | 1 | 0,02% | 1 | 0,19% | 0 | 0% | 1 | 0,2% |
Berry et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bos et al. (2018) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Bosser & Heine (2000) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Bubani & Penzig (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1815) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Colli-Silva et al. (2024) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Cremers & Hoff (2000) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Delprete & Kirkbride (2015) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Don (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz-Sheridan & Portecop (1987) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Gentry (1980) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Gere (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guillaumin (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrington & Gadek (2009) | 1 | 0,02% | 1 | 0,19% | 0 | 0% | 1 | 0,2% |
Harrington (2008) | 1 | 0,02% | 1 | 0,19% | 0 | 0% | 1 | 0,2% |
Hollowell et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaastra (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Landrum (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubengayer et al. (2012) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Linnaeus (1763) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lobreau-callen (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Löfstrand et al. (2021) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Lowry & Plunkett (2020) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Maas & Westra (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Manzitto‐Tripp et al. (2021) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Marais (1997) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Maya-Lastra & Steinmann (2018) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
McVaugh (1969) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Méndez Santos (2001) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Mestier et al. (2022) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Meyer et al. (2008) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Meyer (2017) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Moench (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1933) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Mori et al. (2002) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Nyman (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Pennington (2003) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Persoon (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Plowman & Hensold (2004) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Prance & Sothers (2003) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Prance et al. (2007) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Questel (2022) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Ridley (2022) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Rivière (2003) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Rollet et al. (2010) | 1 | 0,02% | 1 | 0,19% | 0 | 0% | 1 | 0,2% |
Sachet (1962) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Sagot (1881) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Sagot (1882) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Silva & Azevedo Tozzi (2012) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Silva et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stafleu & Cowan (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stehlé & Stehlé (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevenson (1991) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Tassin et al. (2006) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Taylor et al. (2017) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Taylor (1997) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Toutain (1989) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Tsou & Vijayan (2016) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Turner & Veldkamp (2009) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Villanueva-almanza et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vischer (1919) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Webster (1956) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 0 | 0% |
Webster (1958) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Terebinthaceae"(Anacardiaceae and Burseraceae). Frontiers in Genetics, 5(409): 1-20.">Weeks et al. (2014) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Wiersema et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yuan et al. (2010) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |
Zakardjian et al. (2020) | 1 | 0,02% | 1 | 0,19% | 1 | 0,2% | 1 | 0,2% |