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 | 134.17% | 1227 | 178.08% | 1159 | 181.09% | 1213 | 184.63% |
| Florschütz-de Waard et al. (2011) | 163 | 12.4% | 115 | 16.69% | 105 | 16.41% | 107 | 16.29% |
| Gradstein & Ilkiu-Borges (2009) | 143 | 10.88% | 107 | 15.53% | 104 | 16.25% | 102 | 15.53% |
| Boggan et al. (1997) | 132 | 10.05% | 36 | 5.22% | 35 | 5.47% | 35 | 5.33% |
| Gradstein & Hekking (1989) | 126 | 9.59% | 4 | 0.58% | 4 | 0.62% | 4 | 0.61% |
| Thouvenot et al. (2011) | 113 | 8.6% | 27 | 3.92% | 27 | 4.22% | 26 | 3.96% |
| Bardat et al. (2021) | 91 | 6.93% | 20 | 2.9% | 20 | 3.12% | 18 | 2.74% |
| Thouvenot & Bardat (2010) | 87 | 6.62% | 28 | 4.06% | 27 | 4.22% | 26 | 3.96% |
| Lavocat Bernard (2018) | 70 | 5.33% | 59 | 8.56% | 52 | 8.12% | 59 | 8.98% |
| Wigginton (2009) | 40 | 3.04% | 20 | 2.9% | 20 | 3.12% | 19 | 2.89% |
| O’Shea (2006) | 37 | 2.82% | 29 | 4.21% | 25 | 3.91% | 28 | 4.26% |
| Gradstein & Lavocat Bernard (2020) | 35 | 2.66% | 15 | 2.18% | 15 | 2.34% | 13 | 1.98% |
| Reeb et al. (2022) | 33 | 2.51% | 16 | 2.32% | 16 | 2.5% | 16 | 2.44% |
| Hill et al. (2006) | 30 | 2.28% | 7 | 1.02% | 7 | 1.09% | 6 | 0.91% |
| Dauphin (2003) | 26 | 1.98% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts & Lockhart (2020) | 25 | 1.9% | 24 | 3.48% | 23 | 3.59% | 20 | 3.04% |
| Grolle (1995) | 21 | 1.6% | 8 | 1.16% | 8 | 1.25% | 7 | 1.07% |
| Ros et al. (2007) | 19 | 1.45% | 9 | 1.31% | 9 | 1.41% | 8 | 1.22% |
| Söderström et al. (2013) | 19 | 1.45% | 7 | 1.02% | 6 | 0.94% | 6 | 0.91% |
| Bruggeman-Nannenga & Arts (2010) | 16 | 1.22% | 9 | 1.31% | 8 | 1.25% | 7 | 1.07% |
| Lavocat Bernard & Reeb (2016) | 16 | 1.22% | 13 | 1.89% | 12 | 1.88% | 13 | 1.98% |
| Ros et al. (2013) | 16 | 1.22% | 9 | 1.31% | 9 | 1.41% | 8 | 1.22% |
| Hugonnot et al. (2017) | 15 | 1.14% | 7 | 1.02% | 7 | 1.09% | 7 | 1.07% |
| Buck (2003) | 14 | 1.07% | 9 | 1.31% | 4 | 0.62% | 9 | 1.37% |
| Carvalho-silva et al. (2017) | 14 | 1.07% | 7 | 1.02% | 7 | 1.09% | 7 | 1.07% |
| Grolle & Long (2000) | 14 | 1.07% | 6 | 0.87% | 6 | 0.94% | 3 | 0.46% |
| 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 | 0.84% | 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 | 0.61% | 5 | 0.73% | 5 | 0.78% | 5 | 0.76% |
| Koponen (2020) | 8 | 0.61% | 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 | 0.46% | 2 | 0.29% | 2 | 0.31% | 2 | 0.3% |
| Thériot et al. (1934) | 6 | 0.46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Véron et al. (2021) | 6 | 0.46% | 4 | 0.58% | 4 | 0.62% | 4 | 0.61% |
| Villarreal & Renner (2014) | 6 | 0.46% | 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% |
