Bryophytes de Guadeloupe
Mousses, Hépatiques et Anthocérotes de Guadeloupe
135 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) | 1717 | 135,52% | 1195 | 182,44% | 1129 | 185,08% | 1181 | 189,26% |
Florschütz-de Waard et al. (2011) | 162 | 12,79% | 114 | 17,4% | 104 | 17,05% | 106 | 16,99% |
Gradstein & Ilkiu-Borges (2009) | 136 | 10,73% | 102 | 15,57% | 99 | 16,23% | 97 | 15,54% |
Boggan et al. (1997) | 129 | 10,18% | 36 | 5,5% | 35 | 5,74% | 35 | 5,61% |
Gradstein & Hekking (1989) | 117 | 9,23% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Thouvenot et al. (2011) | 110 | 8,68% | 26 | 3,97% | 26 | 4,26% | 25 | 4,01% |
Bardat et al. (2021) | 91 | 7,18% | 20 | 3,05% | 20 | 3,28% | 18 | 2,88% |
Thouvenot & Bardat (2010) | 87 | 6,87% | 28 | 4,27% | 27 | 4,43% | 26 | 4,17% |
Lavocat Bernard (2018) | 58 | 4,58% | 47 | 7,18% | 42 | 6,89% | 47 | 7,53% |
Wigginton (2009) | 38 | 3% | 19 | 2,9% | 19 | 3,11% | 18 | 2,88% |
Gradstein & Lavocat Bernard (2020) | 35 | 2,76% | 15 | 2,29% | 15 | 2,46% | 13 | 2,08% |
O’Shea (2006) | 34 | 2,68% | 27 | 4,12% | 24 | 3,93% | 26 | 4,17% |
Reeb et al. (2022) | 33 | 2,6% | 16 | 2,44% | 16 | 2,62% | 16 | 2,56% |
Hill et al. (2006) | 29 | 2,29% | 7 | 1,07% | 7 | 1,15% | 6 | 0,96% |
Dauphin (2003) | 26 | 2,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts & Lockhart (2020) | 24 | 1,89% | 23 | 3,51% | 22 | 3,61% | 19 | 3,04% |
Grolle (1995) | 20 | 1,58% | 7 | 1,07% | 7 | 1,15% | 6 | 0,96% |
Söderström et al. (2013) | 19 | 1,5% | 7 | 1,07% | 6 | 0,98% | 6 | 0,96% |
Ros et al. (2007) | 17 | 1,34% | 8 | 1,22% | 8 | 1,31% | 7 | 1,12% |
Bruggeman-Nannenga & Arts (2010) | 16 | 1,26% | 9 | 1,37% | 8 | 1,31% | 7 | 1,12% |
Grolle & Long (2000) | 16 | 1,26% | 6 | 0,92% | 6 | 0,98% | 3 | 0,48% |
Lavocat Bernard & Reeb (2016) | 16 | 1,26% | 13 | 1,98% | 12 | 1,97% | 13 | 2,08% |
Ros et al. (2013) | 16 | 1,26% | 9 | 1,37% | 9 | 1,48% | 8 | 1,28% |
Hugonnot et al. (2017) | 15 | 1,18% | 7 | 1,07% | 7 | 1,15% | 7 | 1,12% |
Buck (2003) | 14 | 1,1% | 9 | 1,37% | 4 | 0,66% | 9 | 1,44% |
Bruggeman-Nannenga et al. (1994) | 12 | 0,95% | 3 | 0,46% | 0 | 0% | 3 | 0,48% |
Carvalho-silva et al. (2017) | 12 | 0,95% | 6 | 0,92% | 6 | 0,98% | 6 | 0,96% |
Gradstein & Ilkiu-Borges (2015) | 12 | 0,95% | 6 | 0,92% | 6 | 0,98% | 6 | 0,96% |
Majestyk (2011) | 12 | 0,95% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Whittier (1976) | 11 | 0,87% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Gradstein & Costa (2003) | 10 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein (2015) | 10 | 0,79% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pócs et al. (2015) | 9 | 0,71% | 4 | 0,61% | 4 | 0,66% | 4 | 0,64% |
Reese & Mohamed (1985) | 9 | 0,71% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Grolle (2002) | 8 | 0,63% | 5 | 0,76% | 5 | 0,82% | 5 | 0,8% |
Koponen (2020) | 8 | 0,63% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Ah-Peng et al. (2010) | 7 | 0,55% | 5 | 0,76% | 3 | 0,49% | 4 | 0,64% |
Ah-Peng et al. (2010) | 7 | 0,55% | 4 | 0,61% | 4 | 0,66% | 4 | 0,64% |
Ilkiu Borges (2006) | 7 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Passos Bastos & Gradstein (2020) | 7 | 0,55% | 3 | 0,46% | 0 | 0% | 3 | 0,48% |
Salazar Allen (1993) | 7 | 0,55% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Stephani (1908) | 7 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Sukkharak & Gradstein (2014) | 7 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Yu et al. (2014) | 7 | 0,55% | 6 | 0,92% | 3 | 0,49% | 3 | 0,48% |
Hodgetts et al. (2020) | 6 | 0,47% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Pócs & Bernecker (2009) | 6 | 0,47% | 4 | 0,61% | 4 | 0,66% | 3 | 0,48% |
Thériot et al. (1934) | 6 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Villarreal & Renner (2014) | 6 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Atwood (2015) | 5 | 0,39% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Briscoe et al. (2015) | 5 | 0,39% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Kučera et al. (2013) | 5 | 0,39% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Sukkharak & Gradstein (2017) | 5 | 0,39% | 2 | 0,31% | 1 | 0,16% | 1 | 0,16% |
Véron et al. (2021) | 5 | 0,39% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Wei et al. (2014) | 5 | 0,39% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Ye et al. (2015) | 5 | 0,39% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Câmara (2011) | 4 | 0,32% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Enroth et al. (2019) | 4 | 0,32% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Frahm (2010) | 4 | 0,32% | 2 | 0,31% | 1 | 0,16% | 1 | 0,16% |
Lindberg (1865) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Reiner-Drehwald & Grolle (2012) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Schäfer-Verwimp (2014) | 4 | 0,32% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Spence & Ramsay (2005) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulis et al. (2022) | 3 | 0,24% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Czumay et al. (2013) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Dong et al. (2012) | 3 | 0,24% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Etcheberry et al. (1987) | 3 | 0,24% | 3 | 0,46% | 3 | 0,49% | 3 | 0,48% |
Grolle (1972) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
La Farge (2002) | 3 | 0,24% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Shi et al. (2015) | 3 | 0,24% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Söderström et al. (2016) | 3 | 0,24% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Whittier & Miller (1967) | 3 | 0,24% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Wilbraham & Ellis (2010) | 3 | 0,24% | 3 | 0,46% | 2 | 0,33% | 2 | 0,32% |
Bescherelle (1873) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bescherelle (1895) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bescherelle (1895) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bescherelle (1901) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Câmara (2011) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2021) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Ellis et al. (2023) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Engel & Merrill (2004) | 2 | 0,16% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gradstein & Ilkiu-borges (2021) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Heinrichs et al. (2012) | 2 | 0,16% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Heinrichs et al. (2015) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Iwatsuki & Suzuki (1989) | 2 | 0,16% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Meyer & Ah-Peng (2024) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Mitten (1876) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Tan (2013) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochi (1972) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs et al. (2014) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Schäfer-Verwimp & Van Melick (2016) | 2 | 0,16% | 2 | 0,31% | 2 | 0,33% | 2 | 0,32% |
Söderström et al. (2015) | 2 | 0,16% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Spence (2009) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler (1969) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2013) | 2 | 0,16% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ah-Peng & Bardat (2005) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
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 | 0,16% |
Bastos & Gradstein (2020) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% |
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 | 0,16% |
Cordat (1829) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ellis et al. (2016) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ellis et al. (2016) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ellis et al. (2018) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% |
Gama et al. (2015) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gehrig-Downie et al. (2013) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gil-novoa et al. (2023) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Gradstein & Reeb (2018) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Reeb (2022) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Gradstein (2013) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gradstein (2013) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugonnot (2019) | 1 | 0,08% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Le Gallo (1951) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Müller (2012) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Onraedt & Cremers (1980) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% |
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 | 0,16% |
Thouvenot & Müller (2021) | 1 | 0,08% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% |
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 | 0,16% |
Zander (1993) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |