Mousses des îles subantarctiques
Bryidae des îles subantarctiques
124 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Hill et al. (2006) | 92 | 15,03% | 18 | 10% | 17 | 9,94% | 16 | 9,36% |
| Ros et al. (2013) | 89 | 14,54% | 40 | 22,22% | 39 | 22,81% | 37 | 21,64% |
| Hébrard (1970) | 47 | 7,68% | 14 | 7,78% | 14 | 8,19% | 14 | 8,19% |
| Hodgetts & Lockhart (2020) | 46 | 7,52% | 44 | 24,44% | 42 | 24,56% | 41 | 23,98% |
| Ochyra et al. (2008) | 33 | 5,39% | 10 | 5,56% | 8 | 4,68% | 10 | 5,85% |
| Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1884) | 32 | 5,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot & Bardat (2010) | 28 | 4,58% | 7 | 3,89% | 7 | 4,09% | 7 | 4,09% |
| O’Shea (2006) | 25 | 4,08% | 15 | 8,33% | 12 | 7,02% | 14 | 8,19% |
| Etcheberry et al. (1987) | 23 | 3,76% | 13 | 7,22% | 13 | 7,6% | 10 | 5,85% |
| Hugonnot et al. (2017) | 22 | 3,59% | 17 | 9,44% | 17 | 9,94% | 14 | 8,19% |
| Ochi (1972) | 22 | 3,59% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Maier (2010) | 18 | 2,94% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Tixier (1980) | 15 | 2,45% | 5 | 2,78% | 5 | 2,92% | 5 | 2,92% |
| Véron et al. (2021) | 15 | 2,45% | 15 | 8,33% | 15 | 8,77% | 15 | 8,77% |
| Bescherelle (1875) | 14 | 2,29% | 7 | 3,89% | 7 | 4,09% | 7 | 4,09% |
| Brotherus (1906) | 13 | 2,12% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Hodgetts et al. (2020) | 13 | 2,12% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Cardot (1916) | 12 | 1,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (1993) | 10 | 1,63% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Desplanques & Hébrard (1972) | 9 | 1,47% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
| Ochyra et al. (2014) | 9 | 1,47% | 7 | 3,89% | 7 | 4,09% | 7 | 4,09% |
| Ellis et al. (2018) | 8 | 1,31% | 6 | 3,33% | 6 | 3,51% | 6 | 3,51% |
| Ochyra & Bednarek-ochyra (2017) | 8 | 1,31% | 4 | 2,22% | 4 | 2,34% | 4 | 2,34% |
| Blockeel et al. (2010) | 7 | 1,14% | 7 | 3,89% | 7 | 4,09% | 7 | 4,09% |
| Flatberg et al. (2011) | 7 | 1,14% | 7 | 3,89% | 7 | 4,09% | 7 | 4,09% |
| Ellis et al. (2016) | 6 | 0,98% | 4 | 2,22% | 4 | 2,34% | 3 | 1,75% |
| Fedosov et al. (2023) | 6 | 0,98% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Blockeel et al. (2009) | 5 | 0,82% | 5 | 2,78% | 5 | 2,92% | 5 | 2,92% |
| Jimenez & Suarez (2016) | 5 | 0,82% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Mitten (1876) | 5 | 0,82% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochi (1982) | 5 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra (2003) | 5 | 0,82% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Bednarek-ochyra et al. (2018) | 4 | 0,65% | 2 | 1,11% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2015) | 4 | 0,65% | 4 | 2,22% | 2 | 1,17% | 4 | 2,34% |
| Ellis et al. (2017) | 4 | 0,65% | 4 | 2,22% | 4 | 2,34% | 4 | 2,34% |
| Frahm (2010) | 4 | 0,65% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Lavocat Bernard & Schäfer-Verwimp (2011) | 4 | 0,65% | 3 | 1,67% | 3 | 1,75% | 0 | 0% |
| , 4: 321-360.">Matteri (1973) | 4 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Poulsen (2003) | 4 | 0,65% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ochyra (1997) | 4 | 0,65% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Sollman (2016) | 4 | 0,65% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Bruggeman-Nannenga & Arts (2010) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2011) | 3 | 0,49% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
| Ellis et al. (2012) | 3 | 0,49% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ellis et al. (2013) | 3 | 0,49% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ellis et al. (2013) | 3 | 0,49% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ellis et al. (2017) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Fransén (2004) | 3 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karlin et al. (2018) | 3 | 0,49% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
| Majestyk (2011) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochi (1980) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochyra & Bednarek-ochyra (2013) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochyra (2002) | 3 | 0,49% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochyra (2010) | 3 | 0,49% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
| Seppelt (1991) | 3 | 0,49% | 2 | 1,11% | 0 | 0% | 2 | 1,17% |
| Váňa et al. (2010) | 3 | 0,49% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
| Bartlett & Frahm (1983) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bednarek-Ochyra & Plášek (2019) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Blockeel et al. (2007) | 2 | 0,33% | 2 | 1,11% | 1 | 0,58% | 2 | 1,17% |
| Blockeel et al. (2009) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Blockeel et al. (2009) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ellis et al. (2012) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2014) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2015) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2018) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Ellis et al. (2019) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hooker & Wilson (1844) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hyvönen (1991) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ignatov & Huttunen (2002) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ignatov et al. (2020) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| James (1875) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jiménez & Ochyra (2017) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Magill (1982) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mitten (1876) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ochyra & Bednarek-Ochyra (1997) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochyra et al. (1986) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Pedersen (2005) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Pócs (2022) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Rooy et al. (2021) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Spence & Ramsay (2005) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Spence (2022) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Thériot (1924) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
| Thouvenot & Müller (2021) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Vitt (1976) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vitt (1979) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Zander & Brinda (2021) | 2 | 0,33% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Zander (2017) | 2 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Blockeel et al. (2003) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Blockeel et al. (2007) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Blockeel et al. (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brinda et al. (2021) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Dias et al. (2018) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis et al. (2010) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2012) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2013) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2014) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2015) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2016) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2016) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2016) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2017) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2017) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2018) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2018) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ellis et al. (2019) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Fife (1987) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fife (2020) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibb et al. (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hébrard (1970) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Holyoak & Pedersen (2007) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Holyoak (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iwatsuki (1970) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lara et al. (2016) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| McFarland (1988) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muller et al. (2004) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Murray (1988) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Ochyra et al. (2015) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Piippo (1983) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Price & Ellis (2018) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Schlesak et al. (2018) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thouvenot & Bardat (2013) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Váňa et al. (2014) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
| Zander & Hedderson (2016) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zander (1993) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
