Mousses de la Réunion
Bryidae de la Réunion
166 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| O’Shea (2006) | 441 | 37,72% | 376 | 63,95% | 310 | 63,01% | 362 | 70,84% |
| Thouvenot & Bardat (2010) | 170 | 14,54% | 42 | 7,14% | 42 | 8,54% | 33 | 6,46% |
| Hill et al. (2006) | 120 | 10,27% | 34 | 5,78% | 32 | 6,5% | 20 | 3,91% |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 107 | 9,15% | 58 | 9,86% | 54 | 10,98% | 49 | 9,59% |
| Ros et al. (2013) | 101 | 8,64% | 61 | 10,37% | 58 | 11,79% | 41 | 8,02% |
| Hodgetts & Lockhart (2020) | 70 | 5,99% | 70 | 11,9% | 63 | 12,8% | 49 | 9,59% |
| Ah-Peng et al. (2010) | 65 | 5,56% | 61 | 10,37% | 48 | 9,76% | 57 | 11,15% |
| Véron et al. (2021) | 65 | 5,56% | 64 | 10,88% | 46 | 9,35% | 63 | 12,33% |
| Bruggeman-Nannenga & Arts (2010) | 56 | 4,79% | 38 | 6,46% | 33 | 6,71% | 35 | 6,85% |
| Florschütz-de Waard et al. (2011) | 54 | 4,62% | 31 | 5,27% | 30 | 6,1% | 26 | 5,09% |
| Hugonnot et al. (2017) | 34 | 2,91% | 24 | 4,08% | 24 | 4,88% | 16 | 3,13% |
| Bescherelle (1880) | 28 | 2,4% | 7 | 1,19% | 5 | 1,02% | 6 | 1,17% |
| Wilbraham & Ellis (2010) | 24 | 2,05% | 12 | 2,04% | 5 | 1,02% | 12 | 2,35% |
| Etcheberry et al. (1987) | 23 | 1,97% | 19 | 3,23% | 18 | 3,66% | 10 | 1,96% |
| Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1883) | 22 | 1,88% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whittier (1976) | 22 | 1,88% | 9 | 1,53% | 9 | 1,83% | 8 | 1,57% |
| Ah-Peng et al. (2010) | 20 | 1,71% | 18 | 3,06% | 15 | 3,05% | 17 | 3,33% |
| Pócs (2022) | 20 | 1,71% | 19 | 3,23% | 16 | 3,25% | 16 | 3,13% |
| Allen & Magill (2007) | 18 | 1,54% | 7 | 1,19% | 7 | 1,42% | 7 | 1,37% |
| Frahm (2010) | 18 | 1,54% | 13 | 2,21% | 11 | 2,24% | 11 | 2,15% |
| O'Shea (2006) | 18 | 1,54% | 3 | 0,51% | 3 | 0,61% | 3 | 0,59% |
| Enroth et al. (2019) | 17 | 1,45% | 8 | 1,36% | 8 | 1,63% | 8 | 1,57% |
| Ah-Peng (2007) | 14 | 1,2% | 13 | 2,21% | 11 | 2,24% | 12 | 2,35% |
| Hodgetts et al. (2020) | 14 | 1,2% | 4 | 0,68% | 4 | 0,81% | 3 | 0,59% |
| Majestyk (2011) | 14 | 1,2% | 3 | 0,51% | 3 | 0,61% | 3 | 0,59% |
| Bescherelle (1878) | 12 | 1,03% | 7 | 1,19% | 7 | 1,42% | 5 | 0,98% |
| Ochyra et al. (2008) | 12 | 1,03% | 5 | 0,85% | 4 | 0,81% | 4 | 0,78% |
| Alonso et al. (2019) | 11 | 0,94% | 6 | 1,02% | 6 | 1,22% | 6 | 1,17% |
| La Farge (2002) | 11 | 0,94% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Reese & Mohamed (1985) | 11 | 0,94% | 4 | 0,68% | 4 | 0,81% | 3 | 0,59% |
| Fedosov et al. (2023) | 10 | 0,86% | 4 | 0,68% | 4 | 0,81% | 4 | 0,78% |
| Ochi (1972) | 10 | 0,86% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Salazar Allen (1993) | 10 | 0,86% | 4 | 0,68% | 4 | 0,81% | 4 | 0,78% |
| Ah-Peng & Bardat (2005) | 9 | 0,77% | 8 | 1,36% | 6 | 1,22% | 7 | 1,37% |
| Hébrard (1970) | 9 | 0,77% | 3 | 0,51% | 3 | 0,61% | 3 | 0,59% |
| Alonso et al. (2016) | 8 | 0,68% | 5 | 0,85% | 3 | 0,61% | 2 | 0,39% |
| Koponen (2020) | 8 | 0,68% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Ellis & Wilbraham (2008) | 7 | 0,6% | 2 | 0,34% | 1 | 0,2% | 1 | 0,2% |
| Ellis (1988) | 7 | 0,6% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Maier (2010) | 7 | 0,6% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Thouvenot (2019) | 7 | 0,6% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Vitt & Marsh (1988) | 7 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis (2017) | 6 | 0,51% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Renauld (1897) | 6 | 0,51% | 4 | 0,68% | 4 | 0,81% | 4 | 0,78% |
| Ros et al. (2022) | 6 | 0,51% | 3 | 0,51% | 3 | 0,61% | 0 | 0% |
| Spence & Ramsay (2005) | 6 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wilbraham (2021) | 6 | 0,51% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Buck (2003) | 5 | 0,43% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Enroth et al. (2022) | 5 | 0,43% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Fisher (2006) | 5 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flatberg (1983) | 5 | 0,43% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Kučera et al. (2013) | 5 | 0,43% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Lavocat Bernard (2018) | 5 | 0,43% | 1 | 0,17% | 0 | 0% | 1 | 0,2% |
| Mohamed & Reese (1986) | 5 | 0,43% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Pursell (2017) | 5 | 0,43% | 3 | 0,51% | 1 | 0,2% | 2 | 0,39% |
| Wilbraham (2016) | 5 | 0,43% | 3 | 0,51% | 2 | 0,41% | 3 | 0,59% |
| Bednarek-ochyra et al. (2018) | 4 | 0,34% | 2 | 0,34% | 1 | 0,2% | 1 | 0,2% |
| Bescherelle (1875) | 4 | 0,34% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Bescherelle (1895) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bescherelle (1898) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brotherus (1906) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Câmara (2011) | 4 | 0,34% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Cardot (1916) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2014) | 4 | 0,34% | 1 | 0,17% | 0 | 0% | 1 | 0,2% |
| Ellis et al. (2018) | 4 | 0,34% | 3 | 0,51% | 3 | 0,61% | 3 | 0,59% |
| Hassel et al. (2018) | 4 | 0,34% | 4 | 0,68% | 3 | 0,61% | 1 | 0,2% |
| Thouvenot & Müller (2021) | 4 | 0,34% | 3 | 0,51% | 2 | 0,41% | 3 | 0,59% |
| Zander & Hedderson (2016) | 4 | 0,34% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Arts (2005) | 3 | 0,26% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Atwood (2015) | 3 | 0,26% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bell et al. (2015) | 3 | 0,26% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Ellis et al. (2011) | 3 | 0,26% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Frahm & Stech (2006) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frahm (1990) | 3 | 0,26% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Fransén (2004) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iwatsuki & Suzuki (1989) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mitten (1876) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Zijlstra (2004) | 3 | 0,26% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Tixier (1980) | 3 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartram (1933) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beever (2014) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bescherelle (1895) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blockeel et al. (2009) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Carvalho-silva et al. (2017) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Chavoutier & Hugonnot (2013) | 2 | 0,17% | 2 | 0,34% | 1 | 0,2% | 2 | 0,39% |
| Coulis et al. (2022) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Dalton et al. (2012) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2011) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Ellis et al. (2011) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Ellis et al. (2013) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2015) | 2 | 0,17% | 2 | 0,34% | 0 | 0% | 2 | 0,39% |
| Ellis et al. (2016) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Ellis (2011) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis (2017) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Holyoak & Pedersen (2007) | 2 | 0,17% | 2 | 0,34% | 1 | 0,2% | 1 | 0,2% |
| Jiménez et al. (2017) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Kuc (2006) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 1 | 0,2% |
| Lindberg (1865) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyer & Ah-Peng (2024) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Müller & Tan (2013) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (2012) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Olsson et al. (2016) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Orbán & Reese (1990) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Renauld & Cardot (1894) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Renauld (1891) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 2 | 0,39% |
| Sérgio (2006) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot et al. (1934) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1908) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1923) | 2 | 0,17% | 2 | 0,34% | 1 | 0,2% | 2 | 0,39% |
| Thouvenot & Bardat (2013) | 2 | 0,17% | 2 | 0,34% | 2 | 0,41% | 1 | 0,2% |
| Whittier & Miller (1967) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Wilbraham (2007) | 2 | 0,17% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Asthana & Sahu (2015) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bizot (1976) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Blockeel et al. (2007) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Blockeel et al. (2007) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Blockeel et al. (2010) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bruggeman-Nannenga (1997) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Bruggeman-Nannenga (2005) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bruggeman-Nannenga (2009) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Bruggeman-Nannenga (2016) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calabrese (2006) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosby & Buck (2011) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| De Sloover (1986) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desplanques & Hébrard (1972) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dias et al. (2018) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2010) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Ellis et al. (2012) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2014) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2015) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2016) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Ellis et al. (2016) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis et al. (2020) | 1 | 0,09% | 1 | 0,17% | 0 | 0% | 1 | 0,2% |
| Ellis et al. (2024) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ellis (2017) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Enroth (1990) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flora of North America Editorial Committee (2007) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Frahm et al. (1985) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Greven (1996) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Hugonnot & Chavoutier (2015) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Hugonnot (2013) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Meyer (2013) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Muller et al. (2004) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ochi (1982) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra et al. (2008) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra et al. (2015) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 0 | 0% |
| Ochyra (1987) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (1992) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (1997) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Ochyra (1999) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ros et al. (2007) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Schlesak et al. (2018) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séneca & Söderström (2009) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Séneca & Söderström (2011) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Sollman (2000) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spence (2009) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1921) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot et al. (2018) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot (2015) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Váňa et al. (2010) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Váňa et al. (2014) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Wilding & Hedderson (2011) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Wilding et al. (2013) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Wynns (2020) | 1 | 0,09% | 1 | 0,17% | 1 | 0,2% | 1 | 0,2% |
| Zander (1993) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zander (2017) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
