Bryophytes des Antilles françaises
Mousses, Hépatiques et Anthocérotes des Antilles françaises
138 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 1763 | 133,16% | 1227 | 178,08% | 1159 | 181,09% | 1213 | 184,63% |
| Florschütz-de Waard et al. (2011) | 163 | 12,31% | 115 | 16,69% | 105 | 16,41% | 107 | 16,29% |
| Gradstein & Ilkiu-Borges (2009) | 143 | 10,8% | 107 | 15,53% | 104 | 16,25% | 102 | 15,53% |
| Boggan et al. (1997) | 132 | 9,97% | 36 | 5,22% | 35 | 5,47% | 35 | 5,33% |
| Gradstein & Hekking (1989) | 123 | 9,29% | 4 | 0,58% | 4 | 0,62% | 4 | 0,61% |
| Thouvenot et al. (2011) | 113 | 8,53% | 27 | 3,92% | 27 | 4,22% | 26 | 3,96% |
| Bardat et al. (2021) | 91 | 6,87% | 20 | 2,9% | 20 | 3,12% | 18 | 2,74% |
| Thouvenot & Bardat (2010) | 87 | 6,57% | 28 | 4,06% | 27 | 4,22% | 26 | 3,96% |
| Lavocat Bernard (2018) | 70 | 5,29% | 59 | 8,56% | 52 | 8,12% | 59 | 8,98% |
| Wigginton (2009) | 40 | 3,02% | 20 | 2,9% | 20 | 3,12% | 19 | 2,89% |
| O’Shea (2006) | 37 | 2,79% | 29 | 4,21% | 25 | 3,91% | 28 | 4,26% |
| Gradstein & Lavocat Bernard (2020) | 35 | 2,64% | 15 | 2,18% | 15 | 2,34% | 13 | 1,98% |
| Reeb et al. (2022) | 33 | 2,49% | 16 | 2,32% | 16 | 2,5% | 16 | 2,44% |
| Hill et al. (2006) | 30 | 2,27% | 7 | 1,02% | 7 | 1,09% | 6 | 0,91% |
| Dauphin (2003) | 26 | 1,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts & Lockhart (2020) | 25 | 1,89% | 24 | 3,48% | 23 | 3,59% | 20 | 3,04% |
| Grolle (1995) | 21 | 1,59% | 8 | 1,16% | 8 | 1,25% | 7 | 1,07% |
| Ros et al. (2007) | 19 | 1,44% | 9 | 1,31% | 9 | 1,41% | 8 | 1,22% |
| Söderström et al. (2013) | 19 | 1,44% | 7 | 1,02% | 6 | 0,94% | 6 | 0,91% |
| Bruggeman-Nannenga & Arts (2010) | 16 | 1,21% | 9 | 1,31% | 8 | 1,25% | 7 | 1,07% |
| Grolle & Long (2000) | 16 | 1,21% | 6 | 0,87% | 6 | 0,94% | 3 | 0,46% |
| Lavocat Bernard & Reeb (2016) | 16 | 1,21% | 13 | 1,89% | 12 | 1,88% | 13 | 1,98% |
| Ros et al. (2013) | 16 | 1,21% | 9 | 1,31% | 9 | 1,41% | 8 | 1,22% |
| Hugonnot et al. (2017) | 15 | 1,13% | 7 | 1,02% | 7 | 1,09% | 7 | 1,07% |
| Buck (2003) | 14 | 1,06% | 9 | 1,31% | 4 | 0,62% | 9 | 1,37% |
| Carvalho-silva et al. (2017) | 14 | 1,06% | 7 | 1,02% | 7 | 1,09% | 7 | 1,07% |
| Bruggeman-Nannenga et al. (1994) | 12 | 0,91% | 3 | 0,44% | 0 | 0% | 3 | 0,46% |
| Gradstein & Ilkiu-Borges (2015) | 12 | 0,91% | 6 | 0,87% | 6 | 0,94% | 6 | 0,91% |
| Majestyk (2011) | 12 | 0,91% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Whittier (1976) | 11 | 0,83% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Gradstein & Costa (2003) | 10 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein (2015) | 10 | 0,76% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Pócs et al. (2015) | 9 | 0,68% | 4 | 0,58% | 4 | 0,62% | 4 | 0,61% |
| Reese & Mohamed (1985) | 9 | 0,68% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Yu et al. (2014) | 9 | 0,68% | 8 | 1,16% | 3 | 0,47% | 5 | 0,76% |
| Grolle (2002) | 8 | 0,6% | 5 | 0,73% | 5 | 0,78% | 5 | 0,76% |
| Koponen (2020) | 8 | 0,6% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Ah-Peng et al. (2010) | 7 | 0,53% | 4 | 0,58% | 4 | 0,62% | 4 | 0,61% |
| Ah-Peng et al. (2010) | 7 | 0,53% | 5 | 0,73% | 3 | 0,47% | 4 | 0,61% |
| Ilkiu Borges (2006) | 7 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Passos Bastos & Gradstein (2020) | 7 | 0,53% | 3 | 0,44% | 0 | 0% | 3 | 0,46% |
| Pócs & Bernecker (2009) | 7 | 0,53% | 5 | 0,73% | 5 | 0,78% | 4 | 0,61% |
| Salazar Allen (1993) | 7 | 0,53% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Stephani (1908) | 7 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sukkharak & Gradstein (2014) | 7 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts et al. (2020) | 6 | 0,45% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Thériot et al. (1934) | 6 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Véron et al. (2021) | 6 | 0,45% | 4 | 0,58% | 4 | 0,62% | 4 | 0,61% |
| Villarreal & Renner (2014) | 6 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Atwood (2015) | 5 | 0,38% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Briscoe et al. (2015) | 5 | 0,38% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Kučera et al. (2013) | 5 | 0,38% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Sukkharak & Gradstein (2017) | 5 | 0,38% | 2 | 0,29% | 1 | 0,16% | 1 | 0,15% |
| Wei et al. (2014) | 5 | 0,38% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Ye et al. (2015) | 5 | 0,38% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Câmara (2011) | 4 | 0,3% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Enroth et al. (2019) | 4 | 0,3% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Frahm (2010) | 4 | 0,3% | 2 | 0,29% | 1 | 0,16% | 1 | 0,15% |
| Lindberg (1865) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reiner-Drehwald & Grolle (2012) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schäfer-Verwimp (2014) | 4 | 0,3% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Söderström et al. (2016) | 4 | 0,3% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Spence & Ramsay (2005) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coulis et al. (2022) | 3 | 0,23% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Czumay et al. (2013) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dong et al. (2012) | 3 | 0,23% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Etcheberry et al. (1987) | 3 | 0,23% | 3 | 0,44% | 3 | 0,47% | 3 | 0,46% |
| Gradstein (2012) | 3 | 0,23% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Grolle (1972) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Farge (2002) | 3 | 0,23% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Shi et al. (2015) | 3 | 0,23% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Whittier & Miller (1967) | 3 | 0,23% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Wilbraham & Ellis (2010) | 3 | 0,23% | 3 | 0,44% | 2 | 0,31% | 2 | 0,3% |
| Bescherelle (1873) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bescherelle (1895) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bescherelle (1895) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bescherelle (1901) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Câmara (2011) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2021) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Ellis et al. (2023) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Engel & Merrill (2004) | 2 | 0,15% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Gradstein & Ilkiu-borges (2021) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Heinrichs et al. (2012) | 2 | 0,15% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Heinrichs et al. (2015) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Iwatsuki & Suzuki (1989) | 2 | 0,15% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Meyer & Ah-Peng (2024) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Mitten (1876) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller & Tan (2013) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochi (1972) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pócs et al. (2014) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schäfer-Verwimp & Van Melick (2016) | 2 | 0,15% | 2 | 0,29% | 2 | 0,31% | 2 | 0,3% |
| Söderström et al. (2015) | 2 | 0,15% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Spence (2009) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stotler (1969) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2013) | 2 | 0,15% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Ah-Peng & Bardat (2005) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
| Ah-Peng et al. (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ah-Peng (2007) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Bastos & Gradstein (2020) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Bastos (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blockeel et al. (2007) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Bruggeman-Nannenga (2016) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Campelo Da Silva (2018) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Chatchaba et al. (2023) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cordat (1829) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Crosby (1969) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Ellis et al. (2016) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Ellis et al. (2016) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Ellis et al. (2018) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Enroth (1990) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Feldberg et al. (2010) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Gama et al. (2015) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Gehrig-Downie et al. (2013) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Gil-novoa et al. (2023) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
| Gradstein & Reeb (2018) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein & Reeb (2022) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
| Gradstein (2013) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein (2013) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Hodgetts (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hugonnot (2019) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
| Le Gallo (1951) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Müller (2012) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Onraedt & Cremers (1980) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Pócs & Váňa (2015) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
| Pócs (2011) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pócs (2022) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
| Reeb & Gradstein (2020) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Reiner-Drehwald (2009) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schafer-Verwimp & Reiner-Drehwald (2009) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schlesak et al. (2018) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séneca & Söderström (2011) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Thouvenot & Müller (2021) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Tixier (1986) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2014) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Váňa et al. (2014) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vana & Gremmen (2006) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villarreal et al. (2010) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,15% |
| Zander (1993) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
