Bryophytes de Guyane
Mousses, Hépatiques et Anthocérotes de Guyane française
115 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) | 754 | 76,08% | 496 | 98,22% | 464 | 97,89% | 488 | 100,41% |
Florschütz-de Waard et al. (2011) | 267 | 26,94% | 193 | 38,22% | 179 | 37,76% | 186 | 38,27% |
Gradstein & Ilkiu-Borges (2009) | 240 | 24,22% | 187 | 37,03% | 180 | 37,97% | 184 | 37,86% |
Boggan et al. (1997) | 226 | 22,81% | 116 | 22,97% | 113 | 23,84% | 115 | 23,66% |
Gradstein & Hekking (1989) | 158 | 15,94% | 5 | 0,99% | 5 | 1,05% | 5 | 1,03% |
Thouvenot et al. (2011) | 149 | 15,04% | 36 | 7,13% | 36 | 7,59% | 33 | 6,79% |
Bardat et al. (2021) | 104 | 10,49% | 22 | 4,36% | 22 | 4,64% | 21 | 4,32% |
Thouvenot & Bardat (2010) | 69 | 6,96% | 17 | 3,37% | 16 | 3,38% | 16 | 3,29% |
Buck (2003) | 32 | 3,23% | 20 | 3,96% | 14 | 2,95% | 20 | 4,12% |
Lavocat Bernard (2018) | 31 | 3,13% | 26 | 5,15% | 25 | 5,27% | 26 | 5,35% |
Wigginton (2009) | 31 | 3,13% | 21 | 4,16% | 21 | 4,43% | 19 | 3,91% |
O’Shea (2006) | 30 | 3,03% | 22 | 4,36% | 19 | 4,01% | 22 | 4,53% |
Dauphin (2003) | 26 | 2,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle (1995) | 17 | 1,72% | 9 | 1,78% | 9 | 1,9% | 8 | 1,65% |
Söderström et al. (2013) | 16 | 1,61% | 6 | 1,19% | 4 | 0,84% | 5 | 1,03% |
Reeb et al. (2022) | 15 | 1,51% | 6 | 1,19% | 6 | 1,27% | 6 | 1,23% |
Carvalho-silva et al. (2017) | 14 | 1,41% | 8 | 1,58% | 8 | 1,69% | 8 | 1,65% |
Enroth et al. (2019) | 14 | 1,41% | 6 | 1,19% | 6 | 1,27% | 6 | 1,23% |
Bruggeman-Nannenga & Arts (2010) | 12 | 1,21% | 7 | 1,39% | 7 | 1,48% | 6 | 1,23% |
Gradstein & Costa (2003) | 12 | 1,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Lavocat Bernard (2020) | 10 | 1,01% | 4 | 0,79% | 4 | 0,84% | 3 | 0,62% |
Gradstein (2015) | 10 | 1,01% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Grolle (2002) | 10 | 1,01% | 4 | 0,79% | 4 | 0,84% | 4 | 0,82% |
Lavocat Bernard & Reeb (2016) | 10 | 1,01% | 8 | 1,58% | 8 | 1,69% | 8 | 1,65% |
Reese & Mohamed (1985) | 9 | 0,91% | 3 | 0,59% | 3 | 0,63% | 3 | 0,62% |
Sukkharak & Gradstein (2017) | 9 | 0,91% | 4 | 0,79% | 3 | 0,63% | 3 | 0,62% |
Hill et al. (2006) | 8 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Thériot et al. (1934) | 8 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Whittier (1976) | 8 | 0,81% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Ah-Peng et al. (2010) | 7 | 0,71% | 4 | 0,79% | 4 | 0,84% | 4 | 0,82% |
Grolle & Long (2000) | 7 | 0,71% | 3 | 0,59% | 3 | 0,63% | 2 | 0,41% |
Hodgetts & Lockhart (2020) | 7 | 0,71% | 7 | 1,39% | 7 | 1,48% | 6 | 1,23% |
Ilkiu Borges (2006) | 7 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
Passos Bastos & Gradstein (2020) | 7 | 0,71% | 3 | 0,59% | 0 | 0% | 3 | 0,62% |
Sukkharak & Gradstein (2014) | 7 | 0,71% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Ilkiu-Borges (2015) | 6 | 0,61% | 3 | 0,59% | 3 | 0,63% | 3 | 0,62% |
Ros et al. (2007) | 6 | 0,61% | 4 | 0,79% | 4 | 0,84% | 4 | 0,82% |
Ah-Peng et al. (2010) | 5 | 0,5% | 4 | 0,79% | 3 | 0,63% | 3 | 0,62% |
Alonso et al. (2019) | 5 | 0,5% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Atwood (2015) | 5 | 0,5% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Gehrig-Downie et al. (2013) | 5 | 0,5% | 5 | 0,99% | 5 | 1,05% | 5 | 1,03% |
Majestyk (2011) | 5 | 0,5% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Shi et al. (2015) | 5 | 0,5% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Hugonnot et al. (2017) | 4 | 0,4% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Reiner-Drehwald & Grolle (2012) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Spence & Ramsay (2005) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilbraham & Ellis (2010) | 4 | 0,4% | 4 | 0,79% | 2 | 0,42% | 3 | 0,62% |
Câmara (2011) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Czumay et al. (2013) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein (2012) | 3 | 0,3% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gradstein (2013) | 3 | 0,3% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Kučera et al. (2013) | 3 | 0,3% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Meyer & Ah-Peng (2024) | 3 | 0,3% | 3 | 0,59% | 3 | 0,63% | 3 | 0,62% |
Pócs & Bernecker (2009) | 3 | 0,3% | 2 | 0,4% | 2 | 0,42% | 1 | 0,21% |
Söderström et al. (2016) | 3 | 0,3% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Wei et al. (2014) | 3 | 0,3% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Alonso et al. (2016) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bechteler et al. (2017) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Bescherelle (1873) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bescherelle (1895) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bescherelle (1901) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Briscoe et al. (2015) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Câmara (2011) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2021) | 2 | 0,2% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Ellis et al. (2023) | 2 | 0,2% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Engel & Merrill (2004) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Gil-novoa et al. (2023) | 2 | 0,2% | 2 | 0,4% | 0 | 0% | 2 | 0,41% |
Heinrichs et al. (2012) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Hodgetts et al. (2020) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Iwatsuki & Suzuki (1989) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
La Farge (2002) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Lindberg (1865) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Tan (2013) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs et al. (2015) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Reiner-Drehwald & Schäfer-Verwimp (2008) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Schäfer-Verwimp (2014) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Shu et al. (2016) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Söderström et al. (2015) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Stephani (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler (1969) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot & Müller (2021) | 2 | 0,2% | 2 | 0,4% | 2 | 0,42% | 2 | 0,41% |
Váňa et al. (2013) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Whittier & Miller (1967) | 2 | 0,2% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ah-Peng & Bardat (2009) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ah-Peng et al. (2008) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ah-Peng (2007) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Allen & Magill (2007) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Bastos & Gradstein (2020) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Bastos (2012) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruggeman-Nannenga (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Chatchaba et al. (2023) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulis et al. (2022) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ellis et al. (2018) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Ellis (2017) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Enroth (1990) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein & Reeb (2018) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Heinrichs et al. (1999) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts (2008) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Gallo (1951) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Lee et al. (2018) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (2012) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Pócs et al. (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs (2011) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs (2022) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Reeb & Gradstein (2020) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Reiner-Drehwald (2009) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2013) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Schafer-Verwimp & Reiner-Drehwald (2009) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schäfer-Verwimp & Van Melick (2016) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Shu & Zhu (2019) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler & Crandall-Stotler (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot et al. (2018) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Thouvenot (2023) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Váňa et al. (2014) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |
Wynns (2020) | 1 | 0,1% | 1 | 0,2% | 1 | 0,21% | 1 | 0,21% |