Bryophytes de Polynésie
Mousses, Hépatiques et Anthocérotes de Polynésie française
110 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 | 81.99% | 202 | 85.23% | 183 | 84.72% | 189 | 85.91% |
| Thouvenot et al. (2011) | 529 | 61.09% | 112 | 47.26% | 107 | 49.54% | 98 | 44.55% |
| Thouvenot & Bardat (2010) | 82 | 9.47% | 14 | 5.91% | 13 | 6.02% | 13 | 5.91% |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 63 | 7.27% | 36 | 15.19% | 36 | 16.67% | 32 | 14.55% |
| Wigginton (2009) | 49 | 5.66% | 31 | 13.08% | 31 | 14.35% | 26 | 11.82% |
| Grolle (1995) | 36 | 4.16% | 6 | 2.53% | 6 | 2.78% | 6 | 2.73% |
| Koponen (2020) | 29 | 3.35% | 11 | 4.64% | 11 | 5.09% | 11 | 5% |
| Whittier (1976) | 29 | 3.35% | 28 | 11.81% | 28 | 12.96% | 28 | 12.73% |
| Boggan et al. (1997) | 26 | 3% | 4 | 1.69% | 4 | 1.85% | 3 | 1.36% |
| O'Shea (2006) | 21 | 2.42% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Gradstein & Ilkiu-Borges (2009) | 20 | 2.31% | 17 | 7.17% | 17 | 7.87% | 15 | 6.82% |
| Whittier & Miller (1967) | 16 | 1.85% | 15 | 6.33% | 15 | 6.94% | 15 | 6.82% |
| Gradstein & Hekking (1989) | 14 | 1.62% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Hodgetts & Lockhart (2020) | 14 | 1.62% | 13 | 5.49% | 13 | 6.02% | 9 | 4.09% |
| Ros et al. (2007) | 13 | 1.5% | 9 | 3.8% | 9 | 4.17% | 6 | 2.73% |
| Bruggeman-Nannenga et al. (1994) | 12 | 1.39% | 4 | 1.69% | 1 | 0.46% | 4 | 1.82% |
| Reese & Mohamed (1985) | 12 | 1.39% | 7 | 2.95% | 7 | 3.24% | 7 | 3.18% |
| Bescherelle (1898) | 10 | 1.15% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Sukkharak & Gradstein (2014) | 10 | 1.15% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Bescherelle (1898) | 9 | 1.04% | 9 | 3.8% | 9 | 4.17% | 9 | 4.09% |
| Chua et al. (2018) | 9 | 1.04% | 4 | 1.69% | 2 | 0.93% | 2 | 0.91% |
| Dauphin (2003) | 9 | 1.04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ångström (1873) | 8 | 0.92% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Bescherelle (1895) | 8 | 0.92% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Sukkharak & Gradstein (2017) | 8 | 0.92% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Câmara (2011) | 7 | 0.81% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Grolle & Long (2000) | 7 | 0.81% | 3 | 1.27% | 3 | 1.39% | 2 | 0.91% |
| O’Shea (2006) | 7 | 0.81% | 5 | 2.11% | 5 | 2.31% | 5 | 2.27% |
| Pócs (2011) | 7 | 0.81% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Ellis (2017) | 6 | 0.69% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Hugonnot et al. (2017) | 6 | 0.69% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Kuc (2006) | 6 | 0.69% | 6 | 2.53% | 6 | 2.78% | 6 | 2.73% |
| Thouvenot (2019) | 6 | 0.69% | 3 | 1.27% | 1 | 0.46% | 3 | 1.36% |
| Hodgetts et al. (2020) | 5 | 0.58% | 2 | 0.84% | 1 | 0.46% | 2 | 0.91% |
| Meyer (2013) | 5 | 0.58% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Thouvenot & Müller (2021) | 5 | 0.58% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Thouvenot (2023) | 5 | 0.58% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Váňa et al. (2013) | 5 | 0.58% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Ah-Peng et al. (2010) | 4 | 0.46% | 2 | 0.84% | 1 | 0.46% | 2 | 0.91% |
| Buck (1987) | 4 | 0.46% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Grolle (2002) | 4 | 0.46% | 3 | 1.27% | 3 | 1.39% | 2 | 0.91% |
| Nadeaud (1873) | 4 | 0.46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Söderström et al. (2016) | 4 | 0.46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiers (1993) | 4 | 0.46% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Tixier (1993) | 4 | 0.46% | 4 | 1.69% | 4 | 1.85% | 4 | 1.82% |
| Váňa et al. (2013) | 4 | 0.46% | 2 | 0.84% | 1 | 0.46% | 1 | 0.45% |
| Yu et al. (2014) | 4 | 0.46% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Briscoe et al. (2015) | 3 | 0.35% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ellis et al. (2014) | 3 | 0.35% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Fife (2019) | 3 | 0.35% | 3 | 1.27% | 3 | 1.39% | 3 | 1.36% |
| Iwatsuki & Suzuki (1989) | 3 | 0.35% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Menzel (1992) | 3 | 0.35% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Nishimura (1985) | 3 | 0.35% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Villarreal et al. (2015) | 3 | 0.35% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Yu & Jia (2015) | 3 | 0.35% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Allen (1986) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Bechteler et al. (2017) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Bescherelle (1901) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Cooper et al. (2013) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Florschütz-de Waard et al. (2011) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Frahm (1987) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Katagiri (2015) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Farge (2002) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Meyer & Ah-Peng (2024) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 1 | 0.45% |
| Montagne (1843) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patzak et al. (2016) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Pócs (2011) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Qiu et al. (2014) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reiner-Drehwald & Grolle (2012) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salazar Allen (1993) | 2 | 0.23% | 2 | 0.84% | 2 | 0.93% | 2 | 0.91% |
| Shi et al. (2015) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Shu & Zhu (2019) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Stephani (1908) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot et al. (2018) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Tixier (1986) | 2 | 0.23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2013) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Véron et al. (2021) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Wilbraham (2007) | 2 | 0.23% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ah-Peng & Bardat (2005) | 1 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ah-Peng & Bardat (2009) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ah-Peng et al. (2010) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ångström (1876) | 1 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartram (1933) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Bruggeman-Nannenga & Arts (2010) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Cargill et al. (2013) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Cordat (1829) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Coulis et al. (2022) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ellis et al. (2015) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ellis et al. (2018) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Frahm (1997) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Gradstein & Costa (2003) | 1 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gradstein & Ilkiu-Borges (2015) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Gradstein (2013) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 0 | 0% |
| Gradstein (2015) | 1 | 0.12% | 1 | 0.42% | 0 | 0% | 1 | 0.45% |
| Iwatsuki & Suzuki (1996) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Lavocat Bernard & Reeb (2016) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Lavocat Bernard (2018) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Le Gallo (1951) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Mohamed & Reese (1986) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Ochyra (1997) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Pócs (2016) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Pursell (2002) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Reeb et al. (2022) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Söderström et al. (2023) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Sukkharak (2015) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
| Sun et al. (2018) | 1 | 0.12% | 1 | 0.42% | 0 | 0% | 1 | 0.45% |
| Thériot (1921) | 1 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2013) | 1 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Váňa et al. (2014) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 0 | 0% |
| Wilbraham (2016) | 1 | 0.12% | 1 | 0.42% | 1 | 0.46% | 1 | 0.45% |
