Mousses des îles subantarctiques
Bryidae des îles subantarctiques
133 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% |
Ochyra et al. (2008) | 81 | 13,24% | 47 | 26,11% | 44 | 25,73% | 47 | 27,49% |
Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie, 5: 76–83.">Müller (1883) | 70 | 11,44% | 16 | 8,89% | 16 | 9,36% | 16 | 9,36% |
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% |
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% |
Bescherelle (1875) | 18 | 2,94% | 11 | 6,11% | 11 | 6,43% | 11 | 6,43% |
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% |
Brotherus (1906) | 14 | 2,29% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
Hodgetts et al. (2020) | 14 | 2,29% | 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% |
Hooker & Wilson (1844) | 8 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitten (1876) | 8 | 1,31% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
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% |
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% |
Brinda et al. (2021) | 4 | 0,65% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
Ellis et al. (2013) | 4 | 0,65% | 2 | 1,11% | 2 | 1,17% | 2 | 1,17% |
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. (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% |
Price & Ellis (2018) | 3 | 0,49% | 3 | 1,67% | 3 | 1,75% | 3 | 1,75% |
Robinson (1875) | 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% |
Wynns (2020) | 3 | 0,49% | 3 | 1,67% | 1 | 0,58% | 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. (2007) | 2 | 0,33% | 2 | 1,11% | 2 | 1,17% | 1 | 0,58% |
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. (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% |
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% |
Ochyra (1998) | 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% |
Bednarek-Ochyra (2015) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
Bednarek-Ochyra (2018) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
Blockeel et al. (2003) | 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% |
Blockeel et al. (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
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. (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% |
Meyer & Ah-Peng (2024) | 1 | 0,16% | 1 | 0,56% | 1 | 0,58% | 1 | 0,58% |
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 & Suárez (2011) | 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% |
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% |
Whittier (1976) | 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% |