Bryophytes des îles subantarctiques
Mousses, Hépatiques et Anthocérotes des îles subantarctiques
187 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 | 15.79% | 14 | 4.98% | 14 | 5.3% | 14 | 5.28% |
Ochyra et al. (2008) | 148 | 14.61% | 49 | 17.44% | 45 | 17.05% | 48 | 18.11% |
Grolle (2002) | 147 | 14.51% | 48 | 17.08% | 45 | 17.05% | 46 | 17.36% |
Hill et al. (2006) | 99 | 9.77% | 21 | 7.47% | 20 | 7.58% | 18 | 6.79% |
Ros et al. (2013) | 95 | 9.38% | 44 | 15.66% | 43 | 16.29% | 40 | 15.09% |
Hodgetts & Lockhart (2020) | 63 | 6.22% | 61 | 21.71% | 59 | 22.35% | 55 | 20.75% |
Hébrard (1970) | 48 | 4.74% | 14 | 4.98% | 14 | 5.3% | 14 | 5.28% |
Váňa et al. (2014) | 37 | 3.65% | 34 | 12.1% | 31 | 11.74% | 33 | 12.45% |
Hugonnot et al. (2017) | 33 | 3.26% | 26 | 9.25% | 26 | 9.85% | 20 | 7.55% |
O’Shea (2006) | 30 | 2.96% | 17 | 6.05% | 13 | 4.92% | 16 | 6.04% |
Thouvenot & Bardat (2010) | 28 | 2.76% | 7 | 2.49% | 7 | 2.65% | 7 | 2.64% |
Etcheberry et al. (1987) | 26 | 2.57% | 14 | 4.98% | 14 | 5.3% | 11 | 4.15% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 24 | 2.37% | 12 | 4.27% | 12 | 4.55% | 8 | 3.02% |
Wigginton (2009) | 23 | 2.27% | 14 | 4.98% | 13 | 4.92% | 14 | 5.28% |
Ochi (1972) | 22 | 2.17% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Bescherelle (1875) | 21 | 2.07% | 11 | 3.91% | 11 | 4.17% | 11 | 4.15% |
Véron et al. (2021) | 20 | 1.97% | 20 | 7.12% | 20 | 7.58% | 20 | 7.55% |
Brotherus (1906) | 19 | 1.88% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Grolle (1995) | 18 | 1.78% | 1 | 0.36% | 1 | 0.38% | 0 | 0% |
Maier (2010) | 18 | 1.78% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Bednarek-ochyra (2014) | 16 | 1.58% | 0 | 0% | 0 | 0% | 0 | 0% |
Tixier (1980) | 15 | 1.48% | 5 | 1.78% | 5 | 1.89% | 5 | 1.89% |
Cardot (1916) | 14 | 1.38% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts et al. (2020) | 14 | 1.38% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ros et al. (2007) | 13 | 1.28% | 10 | 3.56% | 10 | 3.79% | 8 | 3.02% |
Grolle & Long (2000) | 10 | 0.99% | 8 | 2.85% | 8 | 3.03% | 7 | 2.64% |
Ochyra (1993) | 10 | 0.99% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Desplanques & Hébrard (1972) | 9 | 0.89% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Mitten (1876) | 9 | 0.89% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra et al. (2014) | 9 | 0.89% | 7 | 2.49% | 7 | 2.65% | 7 | 2.64% |
Thouvenot et al. (2011) | 9 | 0.89% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Ellis et al. (2018) | 8 | 0.79% | 6 | 2.14% | 6 | 2.27% | 6 | 2.26% |
Hooker & Wilson (1844) | 8 | 0.79% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra & Bednarek-ochyra (2017) | 8 | 0.79% | 4 | 1.42% | 4 | 1.52% | 4 | 1.51% |
Blockeel et al. (2010) | 7 | 0.69% | 7 | 2.49% | 7 | 2.65% | 7 | 2.64% |
Flatberg et al. (2011) | 7 | 0.69% | 7 | 2.49% | 7 | 2.65% | 7 | 2.64% |
Ochyra & Suárez (2011) | 7 | 0.69% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Váňa et al. (2013) | 7 | 0.69% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Vitt & Marsh (1988) | 7 | 0.69% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2009) | 6 | 0.59% | 6 | 2.14% | 6 | 2.27% | 6 | 2.26% |
Ellis et al. (2016) | 6 | 0.59% | 4 | 1.42% | 4 | 1.52% | 3 | 1.13% |
Fedosov et al. (2023) | 6 | 0.59% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Feldberg et al. (2010) | 6 | 0.59% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Fransén (2004) | 6 | 0.59% | 2 | 0.71% | 0 | 0% | 2 | 0.75% |
IV. Botanik. Ernst Siegfried Mittler und Sohn, Berlin, Germany: 1-64.">Müller (1889) | 6 | 0.59% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2010) | 6 | 0.59% | 5 | 1.78% | 5 | 1.89% | 5 | 1.89% |
Jimenez & Suarez (2016) | 5 | 0.49% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochi (1982) | 5 | 0.49% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra (2003) | 5 | 0.49% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Söderström et al. (2013) | 5 | 0.49% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Sollman (2016) | 5 | 0.49% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Bednarek-ochyra et al. (2018) | 4 | 0.39% | 2 | 0.71% | 1 | 0.38% | 1 | 0.38% |
Brinda et al. (2021) | 4 | 0.39% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Briscoe et al. (2015) | 4 | 0.39% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ellis et al. (2013) | 4 | 0.39% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ellis et al. (2015) | 4 | 0.39% | 4 | 1.42% | 2 | 0.76% | 4 | 1.51% |
Ellis et al. (2017) | 4 | 0.39% | 4 | 1.42% | 4 | 1.52% | 4 | 1.51% |
Frahm (2010) | 4 | 0.39% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Hentschel et al. (2007) | 4 | 0.39% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts (2008) | 4 | 0.39% | 0 | 0% | 0 | 0% | 0 | 0% |
, 4: 321-360.">Matteri (1973) | 4 | 0.39% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra & Poulsen (2003) | 4 | 0.39% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ochyra (1997) | 4 | 0.39% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Bardat et al. (2021) | 3 | 0.3% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Bednarek-Ochyra (2015) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Blockeel et al. (2009) | 3 | 0.3% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Boggan et al. (1997) | 3 | 0.3% | 3 | 1.07% | 3 | 1.14% | 2 | 0.75% |
Bruggeman-Nannenga & Arts (2010) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Cardot (1908) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Deguchi (1984) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2011) | 3 | 0.3% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Ellis et al. (2012) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2013) | 3 | 0.3% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ellis et al. (2017) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Gradstein & Ilkiu-Borges (2009) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
James (1875) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Karlin et al. (2018) | 3 | 0.3% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Kramer (1988) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Majestyk (2011) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochi (1980) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra & Bednarek-ochyra (2013) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra (1998) | 3 | 0.3% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ochyra (2002) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra (2010) | 3 | 0.3% | 3 | 1.07% | 3 | 1.14% | 3 | 1.13% |
Price & Ellis (2018) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Robinson (1875) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuette & Stotler 2005) | 3 | 0.3% | 0 | 0% | 0 | 0% | 0 | 0% |
Seppelt (1991) | 3 | 0.3% | 2 | 0.71% | 0 | 0% | 2 | 0.75% |
Söderström et al. (2016) | 3 | 0.3% | 2 | 0.71% | 2 | 0.76% | 1 | 0.38% |
Váňa et al. (2014) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Vana & Gremmen (2006) | 3 | 0.3% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Wynns (2020) | 3 | 0.3% | 3 | 1.07% | 1 | 0.38% | 2 | 0.75% |
Bartlett & Frahm (1983) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bednarek-Ochyra & Plášek (2019) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Blockeel et al. (2007) | 2 | 0.2% | 2 | 0.71% | 1 | 0.38% | 2 | 0.75% |
Blockeel et al. (2007) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 1 | 0.38% |
Blockeel et al. (2009) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ellis et al. (2012) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2014) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2015) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2018) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 1 | 0.38% |
Ellis et al. (2018) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Ellis et al. (2019) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyvönen (1991) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hyvönen (2006) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ignatov & Huttunen (2002) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ignatov et al. (2020) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Jiménez & Ochyra (2017) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
La Farge (2002) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Gallo (1951) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Magill (1982) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer & Ah-Peng (2024) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Mitten (1876) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Philosophical Transactions of the Royal Society of London, 168: 24-39.">Mitten (1879) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra & Bednarek-Ochyra (1997) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra et al. (1986) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Pedersen (2005) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Plášek et al. (2015) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Pócs (2022) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Rooy et al. (2021) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Schiffner (1906) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Shaw et al. (2015) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Spence & Ramsay (2005) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Spence (2022) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Suárez & Schiavone (2011) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Thériot (1924) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Thouvenot & Müller (2021) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Váňa & Gremmen (2005) | 2 | 0.2% | 2 | 0.71% | 2 | 0.76% | 2 | 0.75% |
Váňa & Long (2011) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2010) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Váňa et al. (2013) | 2 | 0.2% | 1 | 0.36% | 0 | 0% | 1 | 0.38% |
Vitt (1976) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Vitt (1979) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Zander & Brinda (2021) | 2 | 0.2% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Zander (2017) | 2 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ah-Peng et al. (2008) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ah-Peng (2007) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Bednarek-Ochyra (2018) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Blockeel et al. (2003) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Blockeel et al. (2008) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2008) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Calabrese (2006) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
De Sloover (1986) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dias et al. (2018) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dixon (1914) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2010) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2012) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2012) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2013) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2014) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2015) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2016) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2016) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2016) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2017) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2017) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2018) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ellis et al. (2019) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Fife (1987) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fife (2020) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibb et al. (2021) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle & Onraedt (1974) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hébrard (1970) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Holyoak & Pedersen (2007) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Holyoak (2021) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Iwatsuki (1970) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lara et al. (2016) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Lavocat Bernard (2018) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 0 | 0% |
McFarland (1988) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2004) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Murray (1988) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra & Bednarek-Ochyra (1991) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra et al. (2015) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Ochyra (1987) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra (1992) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra (1999) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Piippo (1983) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Schlesak et al. (2018) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström et al. (2013) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Stotler & Crandall-Stotler (2017) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot & Bardat (2013) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Thouvenot (2023) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 0 | 0% |
Váňa et al. (2013) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Whittier (1976) | 1 | 0.1% | 1 | 0.36% | 1 | 0.38% | 1 | 0.38% |
Zander & Hedderson (2016) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |
Zander (1993) | 1 | 0.1% | 0 | 0% | 0 | 0% | 0 | 0% |