Mousses des îles subantarctiques
Bryidae des îles subantarctiques
154 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1883) | 160 | 19,61% | 14 | 6,8% | 14 | 7,18% | 14 | 7,18% |
| Ochyra et al. (2008) | 153 | 18,75% | 49 | 23,79% | 45 | 23,08% | 48 | 24,62% |
| Hill et al. (2006) | 99 | 12,13% | 21 | 10,19% | 20 | 10,26% | 18 | 9,23% |
| Ros et al. (2013) | 95 | 11,64% | 44 | 21,36% | 43 | 22,05% | 40 | 20,51% |
| Hodgetts & Lockhart (2020) | 51 | 6,25% | 49 | 23,79% | 47 | 24,1% | 45 | 23,08% |
| Hébrard (1970) | 47 | 5,76% | 14 | 6,8% | 14 | 7,18% | 14 | 7,18% |
| O’Shea (2006) | 31 | 3,8% | 17 | 8,25% | 13 | 6,67% | 16 | 8,21% |
| Thouvenot & Bardat (2010) | 28 | 3,43% | 7 | 3,4% | 7 | 3,59% | 6 | 3,08% |
| Etcheberry et al. (1987) | 26 | 3,19% | 14 | 6,8% | 14 | 7,18% | 10 | 5,13% |
| Hugonnot et al. (2017) | 25 | 3,06% | 20 | 9,71% | 20 | 10,26% | 16 | 8,21% |
| Ochi (1972) | 22 | 2,7% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Bescherelle (1875) | 21 | 2,57% | 11 | 5,34% | 11 | 5,64% | 11 | 5,64% |
| Brotherus (1906) | 19 | 2,33% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Maier (2010) | 18 | 2,21% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Bednarek-ochyra (2014) | 16 | 1,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tixier (1980) | 15 | 1,84% | 5 | 2,43% | 5 | 2,56% | 5 | 2,56% |
| Véron et al. (2021) | 15 | 1,84% | 15 | 7,28% | 15 | 7,69% | 15 | 7,69% |
| Cardot (1916) | 14 | 1,72% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hodgetts et al. (2020) | 14 | 1,72% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ochyra (1993) | 10 | 1,23% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Desplanques & Hébrard (1972) | 9 | 1,1% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Mitten (1876) | 9 | 1,1% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra et al. (2014) | 9 | 1,1% | 7 | 3,4% | 7 | 3,59% | 7 | 3,59% |
| Ellis et al. (2018) | 8 | 0,98% | 6 | 2,91% | 6 | 3,08% | 6 | 3,08% |
| Hooker & Wilson (1844) | 8 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Bednarek-ochyra (2017) | 8 | 0,98% | 4 | 1,94% | 4 | 2,05% | 4 | 2,05% |
| Blockeel et al. (2010) | 7 | 0,86% | 7 | 3,4% | 7 | 3,59% | 7 | 3,59% |
| Flatberg et al. (2011) | 7 | 0,86% | 7 | 3,4% | 7 | 3,59% | 7 | 3,59% |
| Ochyra & Suárez (2011) | 7 | 0,86% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Vitt & Marsh (1988) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2016) | 6 | 0,74% | 4 | 1,94% | 4 | 2,05% | 3 | 1,54% |
| Fedosov et al. (2023) | 6 | 0,74% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Fransén (2004) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| IV. Botanik. Ernst Siegfried Mittler und Sohn, Berlin, Germany: 1-64.">Müller (1889) | 6 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blockeel et al. (2009) | 5 | 0,61% | 5 | 2,43% | 5 | 2,56% | 5 | 2,56% |
| Jimenez & Suarez (2016) | 5 | 0,61% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochi (1982) | 5 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (2003) | 5 | 0,61% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Sollman (2016) | 5 | 0,61% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Bednarek-ochyra et al. (2018) | 4 | 0,49% | 2 | 0,97% | 1 | 0,51% | 1 | 0,51% |
| Brinda et al. (2021) | 4 | 0,49% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ellis et al. (2013) | 4 | 0,49% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ellis et al. (2015) | 4 | 0,49% | 4 | 1,94% | 2 | 1,03% | 4 | 2,05% |
| Ellis et al. (2017) | 4 | 0,49% | 4 | 1,94% | 4 | 2,05% | 4 | 2,05% |
| Frahm (2010) | 4 | 0,49% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 4 | 0,49% | 3 | 1,46% | 3 | 1,54% | 0 | 0% |
| , 4: 321-360.">Matteri (1973) | 4 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Poulsen (2003) | 4 | 0,49% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ochyra (1997) | 4 | 0,49% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Bednarek-Ochyra (2015) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Blockeel et al. (2009) | 3 | 0,37% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Bruggeman-Nannenga & Arts (2010) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Cardot (1908) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deguchi (1984) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2011) | 3 | 0,37% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Ellis et al. (2012) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2013) | 3 | 0,37% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ellis et al. (2017) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| James (1875) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karlin et al. (2018) | 3 | 0,37% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Kramer (1988) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Majestyk (2011) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochi (1980) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra & Bednarek-ochyra (2013) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra (1998) | 3 | 0,37% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ochyra (2002) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra (2010) | 3 | 0,37% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Price & Ellis (2018) | 3 | 0,37% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Robinson (1875) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seppelt (1991) | 3 | 0,37% | 2 | 0,97% | 0 | 0% | 2 | 1,03% |
| Váňa et al. (2010) | 3 | 0,37% | 3 | 1,46% | 3 | 1,54% | 3 | 1,54% |
| Wynns (2020) | 3 | 0,37% | 3 | 1,46% | 1 | 0,51% | 2 | 1,03% |
| Bartlett & Frahm (1983) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bednarek-Ochyra & Plášek (2019) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Blockeel et al. (2007) | 2 | 0,25% | 2 | 0,97% | 1 | 0,51% | 2 | 1,03% |
| Blockeel et al. (2007) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 1 | 0,51% |
| Blockeel et al. (2009) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ellis et al. (2012) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2014) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2015) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2018) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Ellis et al. (2018) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 1 | 0,51% |
| Ellis et al. (2019) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyvönen (1991) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyvönen (2006) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ignatov & Huttunen (2002) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ignatov et al. (2020) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Jiménez & Ochyra (2017) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Jiménez et al. (2021) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| La Farge (2002) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magill (1982) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mitten (1876) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philosophical Transactions of the Royal Society of London, 168: 24-39.">Mitten (1879) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Bednarek-Ochyra (1997) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra et al. (1986) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Pedersen (2005) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Plášek et al. (2015) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Pócs (2022) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Rooy et al. (2021) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Spence & Ramsay (2005) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Spence (2022) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Suárez & Schiavone (2011) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thériot (1924) | 2 | 0,25% | 2 | 0,97% | 2 | 1,03% | 2 | 1,03% |
| Thouvenot & Müller (2021) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Vitt (1976) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vitt (1979) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Zander & Brinda (2021) | 2 | 0,25% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Zander (2017) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ah-Peng (2007) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Bednarek-Ochyra (2018) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Blockeel et al. (2003) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Blockeel et al. (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blockeel et al. (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calabrese (2006) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| De Sloover (1986) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dias et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dixon (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2010) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2012) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2013) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2014) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2015) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2016) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2016) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 0 | 0% |
| Ellis et al. (2016) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2017) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2017) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2018) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2019) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ellis et al. (2024) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Fife (1987) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fife (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibb et al. (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hébrard (1970) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Holyoak & Pedersen (2007) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Holyoak (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iwatsuki (1970) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lara et al. (2016) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| McFarland (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyer & Ah-Peng (2024) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Muller et al. (2004) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Murray (1988) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra & Bednarek-Ochyra (1991) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra et al. (2015) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Ochyra (1987) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Piippo (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schlesak et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot & Bardat (2013) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Váňa et al. (2014) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Whittier (1976) | 1 | 0,12% | 1 | 0,49% | 1 | 0,51% | 1 | 0,51% |
| Zander & Hedderson (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zander (1993) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
