Bryophytes de Polynésie
Mousses, Hépatiques et Anthocérotes de Polynésie française
133 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Bardat et al. (2021) | 710 | 70,09% | 202 | 70,88% | 183 | 69,85% | 189 | 71,05% |
| Thouvenot et al. (2011) | 529 | 52,22% | 112 | 39,3% | 107 | 40,84% | 98 | 36,84% |
| Thouvenot & Bardat (2010) | 168 | 16,58% | 42 | 14,74% | 39 | 14,89% | 40 | 15,04% |
| Whittier (1976) | 93 | 9,18% | 35 | 12,28% | 35 | 13,36% | 35 | 13,16% |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 76 | 7,5% | 45 | 15,79% | 45 | 17,18% | 38 | 14,29% |
| Wigginton (2009) | 49 | 4,84% | 31 | 10,88% | 31 | 11,83% | 26 | 9,77% |
| Grolle (1995) | 36 | 3,55% | 6 | 2,11% | 6 | 2,29% | 6 | 2,26% |
| Reese & Mohamed (1985) | 34 | 3,36% | 13 | 4,56% | 13 | 4,96% | 13 | 4,89% |
| Koponen (2020) | 29 | 2,86% | 11 | 3,86% | 11 | 4,2% | 11 | 4,14% |
| Boggan et al. (1997) | 26 | 2,57% | 4 | 1,4% | 4 | 1,53% | 3 | 1,13% |
| Bruggeman-Nannenga et al. (1994) | 26 | 2,57% | 4 | 1,4% | 0 | 0% | 4 | 1,5% |
| Bescherelle (1898) | 21 | 2,07% | 7 | 2,46% | 7 | 2,67% | 7 | 2,63% |
| O'Shea (2006) | 21 | 2,07% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Gradstein & Ilkiu-Borges (2009) | 20 | 1,97% | 17 | 5,96% | 17 | 6,49% | 15 | 5,64% |
| Salazar Allen (1993) | 19 | 1,88% | 7 | 2,46% | 7 | 2,67% | 7 | 2,63% |
| Whittier & Miller (1967) | 18 | 1,78% | 13 | 4,56% | 13 | 4,96% | 13 | 4,89% |
| Bescherelle (1895) | 16 | 1,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts & Lockhart (2020) | 14 | 1,38% | 13 | 4,56% | 13 | 4,96% | 9 | 3,38% |
| O’Shea (2006) | 13 | 1,28% | 11 | 3,86% | 11 | 4,2% | 10 | 3,76% |
| Ros et al. (2007) | 13 | 1,28% | 9 | 3,16% | 9 | 3,44% | 6 | 2,26% |
| Allen (1986) | 10 | 0,99% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Ångström (1873) | 10 | 0,99% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Bescherelle (1898) | 10 | 0,99% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Sukkharak & Gradstein (2014) | 10 | 0,99% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Chua et al. (2018) | 9 | 0,89% | 4 | 1,4% | 2 | 0,76% | 2 | 0,75% |
| Dauphin (2003) | 9 | 0,89% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis (1985) | 9 | 0,89% | 5 | 1,75% | 5 | 1,91% | 5 | 1,88% |
| Gradstein & Hekking (1989) | 9 | 0,89% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Florschütz-de Waard et al. (2011) | 8 | 0,79% | 6 | 2,11% | 6 | 2,29% | 5 | 1,88% |
| Sukkharak & Gradstein (2017) | 8 | 0,79% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Câmara (2011) | 7 | 0,69% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ellis (1988) | 7 | 0,69% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Grolle & Long (2000) | 7 | 0,69% | 3 | 1,05% | 3 | 1,15% | 2 | 0,75% |
| Hugonnot et al. (2017) | 7 | 0,69% | 5 | 1,75% | 5 | 1,91% | 5 | 1,88% |
| Mohamed & Reese (1986) | 7 | 0,69% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Pócs (2011) | 7 | 0,69% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Bescherelle (1895) | 6 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis (2017) | 6 | 0,59% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Frahm (1987) | 6 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts et al. (2020) | 6 | 0,59% | 3 | 1,05% | 2 | 0,76% | 3 | 1,13% |
| Kuc (2006) | 6 | 0,59% | 5 | 1,75% | 5 | 1,91% | 5 | 1,88% |
| Thouvenot (2019) | 6 | 0,59% | 3 | 1,05% | 1 | 0,38% | 3 | 1,13% |
| Bartram (1933) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruggeman-Nannenga & Arts (2010) | 5 | 0,49% | 2 | 0,7% | 2 | 0,76% | 1 | 0,38% |
| Fisher (2006) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyer (2013) | 5 | 0,49% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Thouvenot & Müller (2021) | 5 | 0,49% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Thouvenot (2023) | 5 | 0,49% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Váňa et al. (2013) | 5 | 0,49% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Ah-Peng et al. (2010) | 4 | 0,39% | 2 | 0,7% | 1 | 0,38% | 2 | 0,75% |
| Bescherelle (1873) | 4 | 0,39% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Bescherelle (1901) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buck (1987) | 4 | 0,39% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Fife (2019) | 4 | 0,39% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Grolle (2002) | 4 | 0,39% | 3 | 1,05% | 3 | 1,15% | 2 | 0,75% |
| Lindberg (1865) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nadeaud (1873) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Söderström et al. (2016) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiers (1993) | 4 | 0,39% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Tixier (1993) | 4 | 0,39% | 4 | 1,4% | 4 | 1,53% | 4 | 1,5% |
| Váňa et al. (2013) | 4 | 0,39% | 2 | 0,7% | 1 | 0,38% | 1 | 0,38% |
| Yu et al. (2014) | 4 | 0,39% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Briscoe et al. (2015) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ellis et al. (2014) | 3 | 0,3% | 3 | 1,05% | 3 | 1,15% | 3 | 1,13% |
| Iwatsuki & Suzuki (1989) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 0 | 0% |
| Iwatsuki & Suzuki (1996) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Menzel (1992) | 3 | 0,3% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Meyer & Ah-Peng (2024) | 3 | 0,3% | 3 | 1,05% | 3 | 1,15% | 2 | 0,75% |
| Nishimura (1985) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Reese et al. (1986) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Tixier (1986) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villarreal et al. (2015) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Yu & Jia (2015) | 3 | 0,3% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Bechteler et al. (2017) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Cooper et al. (2013) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ellis (2011) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Frahm (1997) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Katagiri (2015) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Farge (2002) | 2 | 0,2% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Montagne (1843) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (2012) | 2 | 0,2% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Ochyra (1997) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Patzak et al. (2016) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Pócs (2011) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Pursell (2002) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Qiu et al. (2014) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reiner-Drehwald & Grolle (2012) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Renauld (1891) | 2 | 0,2% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Shi et al. (2015) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Shu & Zhu (2019) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Stephani (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot et al. (1934) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1908) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1921) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot et al. (2018) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Tiwutanon et al. (2023) | 2 | 0,2% | 2 | 0,7% | 2 | 0,76% | 2 | 0,75% |
| Váňa et al. (2013) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Véron et al. (2021) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Wilbraham (2007) | 2 | 0,2% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ah-Peng & Bardat (2005) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ah-Peng & Bardat (2009) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ah-Peng et al. (2010) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ångström (1876) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruggeman-Nannenga (2016) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cargill et al. (2013) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Cordat (1829) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Coulis et al. (2022) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ellis et al. (2015) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ellis et al. (2018) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Enroth (1990) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frahm (1992) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frahm (1994) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein & Costa (2003) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein & Ilkiu-Borges (2015) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Gradstein (2013) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 0 | 0% |
| Gradstein (2015) | 1 | 0,1% | 1 | 0,35% | 0 | 0% | 1 | 0,38% |
| Hébrard (1970) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Hill et al. (2006) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Lavocat Bernard & Reeb (2016) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Lavocat Bernard (2018) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 0 | 0% |
| Le Gallo (1951) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Muller et al. (2004) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Ochyra et al. (2008) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Pócs (2016) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Pócs (2022) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Reeb et al. (2022) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Söderström et al. (2023) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Sukkharak (2015) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
| Sun et al. (2018) | 1 | 0,1% | 1 | 0,35% | 0 | 0% | 1 | 0,38% |
| Thériot (1921) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2013) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2014) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 0 | 0% |
| Wilbraham (2016) | 1 | 0,1% | 1 | 0,35% | 1 | 0,38% | 1 | 0,38% |
