Fonge (hors lichens) de Nouvelle-Calédonie
115 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Courtecuisse (2009) | 434 | 28,22% | 60 | 10,6% | 60 | 10,73% | 60 | 10,7% |
Horak & Mouchacca (1998) | 286 | 18,6% | 169 | 29,86% | 165 | 29,52% | 169 | 30,12% |
Courtecuisse & Welti (2013) | 84 | 5,46% | 52 | 9,19% | 52 | 9,3% | 52 | 9,27% |
Mouchacca & Horak (1998) | 66 | 4,29% | 61 | 10,78% | 59 | 10,55% | 61 | 10,87% |
Braun et al. (1999) | 65 | 4,23% | 62 | 10,95% | 61 | 10,91% | 60 | 10,7% |
Huguenin (1969) | 49 | 3,19% | 43 | 7,6% | 41 | 7,33% | 43 | 7,66% |
Papong et al. (2014) | 42 | 2,73% | 40 | 7,07% | 40 | 7,16% | 40 | 7,13% |
Courtecuisse et al. (1996) | 37 | 2,41% | 27 | 4,77% | 27 | 4,83% | 27 | 4,81% |
Buyck (2013) | 26 | 1,69% | 21 | 3,71% | 21 | 3,76% | 21 | 3,74% |
Louwhoff & Elix (2002) | 22 | 1,43% | 22 | 3,89% | 22 | 3,94% | 22 | 3,92% |
Jaouen et al. (2019) | 21 | 1,37% | 15 | 2,65% | 15 | 2,68% | 15 | 2,67% |
Courtecuisse (2006) | 17 | 1,11% | 16 | 2,83% | 16 | 2,86% | 16 | 2,85% |
Aptroot (2014) | 15 | 0,98% | 15 | 2,65% | 15 | 2,68% | 15 | 2,67% |
Braun et al. (2014) | 15 | 0,98% | 15 | 2,65% | 15 | 2,68% | 15 | 2,67% |
Crossay et al. (2018) | 12 | 0,78% | 9 | 1,59% | 9 | 1,61% | 9 | 1,6% |
Eyssartier et al. (2011) | 12 | 0,78% | 12 | 2,12% | 12 | 2,15% | 12 | 2,14% |
Huguenin (1969) | 12 | 0,78% | 12 | 2,12% | 12 | 2,15% | 12 | 2,14% |
Abraham (2021) | 11 | 0,72% | 10 | 1,77% | 10 | 1,79% | 10 | 1,78% |
Aptroot & Lücking (2016) | 11 | 0,72% | 11 | 1,94% | 11 | 1,97% | 11 | 1,96% |
Rivoire (2018) | 9 | 0,59% | 8 | 1,41% | 8 | 1,43% | 8 | 1,43% |
Elix & McCarthy (1998) | 8 | 0,52% | 5 | 0,88% | 5 | 0,89% | 5 | 0,89% |
Anonyme (2018) | 7 | 0,46% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Rogers & Ju (1998) | 7 | 0,46% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Elvebakk et al. (2016) | 6 | 0,39% | 6 | 1,06% | 6 | 1,07% | 6 | 1,07% |
Kistenich et al. (2018) | 6 | 0,39% | 6 | 1,06% | 6 | 1,07% | 6 | 1,07% |
Lécuru & Courtecuisse (2013) | 6 | 0,39% | 5 | 0,88% | 5 | 0,89% | 5 | 0,89% |
Lücking & Kalb (2001) | 6 | 0,39% | 6 | 1,06% | 6 | 1,07% | 6 | 1,07% |
Berndt (2013) | 5 | 0,33% | 5 | 0,88% | 5 | 0,89% | 5 | 0,89% |
Buyck (2014) | 5 | 0,33% | 5 | 0,88% | 5 | 0,89% | 5 | 0,89% |
Corriol & Roy (2021) | 5 | 0,33% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Jorgensen & Gjerde (2012) | 5 | 0,33% | 5 | 0,88% | 5 | 0,89% | 5 | 0,89% |
Questel (2022) | 5 | 0,33% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Eyssartier et al. (2008) | 4 | 0,26% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Pearson et al. (1922) | 4 | 0,26% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Udagawa et al. (1994) | 4 | 0,26% | 4 | 0,71% | 4 | 0,72% | 4 | 0,71% |
Bricaud (2007) | 3 | 0,2% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Buyck et al. (2012) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Ducousso et al. (2004) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Duhem & Buyck (2011) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Duhem & Buyck (2012) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Dupont et al. (2000) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Elix (2009) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Ephytia (2020) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Eyssartier et al. (2010) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Hughes et al. (2004) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Lebel et al. (2015) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Lebel et al. (2018) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Liberato & Barreto (2006) | 3 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Lücking et al. (2016) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
McTaggart et al. (2008) | 3 | 0,2% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
O’Donnell et al. (2022) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Rikkinen et al. (2014) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Rikkinen et al. (2016) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Rivoire (2013) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Ryvarden (2005) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Videira et al. (2017) | 3 | 0,2% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Zaremski et al. (2014) | 3 | 0,2% | 3 | 0,53% | 3 | 0,54% | 3 | 0,53% |
Archer & Elix (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Armada (2018) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Berrin et al. (2012) | 2 | 0,13% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Bon (1999) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonati & Petitmengin (1907) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Buyck et al. (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Buyck (2004) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Corriol (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Deighton (1974) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Döbbeler & Müller (2018) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Döbbeler (2005) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Elix (2019) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Elvebakk (2007) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Eyssartier & Ducousso (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Hale (1976) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Hariot & Patouillard (1903) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Heim (1966) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Hekking & Sipman (1988) | 2 | 0,13% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Hennings (1903) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Huguenin (1964) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Johnston et al. (2022) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Kalb et al. (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Kalb (2008) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Kwaśna & Nirenberg (2005) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Looney et al. (2013) | 2 | 0,13% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Massee (1901) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Mckenzie & Kuthubutheen (1993) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Mckenzie (1995) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
O’donnell et al. (2004) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Schinz (1920) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Smith (1965) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Spooner (1985) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Udagawa et al. (1994) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Vouaux (1910) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Wakefield et al. (1916) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Wei et al. (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,36% | 2 | 0,36% |
Welti & Courtecuisse (2010) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Aime & Mctaggart (2021) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Błaszkowski et al. (2021) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Boidin & Gilles (1989) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Buyck et al. (2016) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Cheype (2010) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Cooper (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dai (2010) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Dennis (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Imshaug (2019) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kalb & Elix (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Leyronas et al. (2004) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Liberato et al. (2005) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Noordeloos et al. (2022) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Padamsee & Mckenzie (2012) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Pée-laby (1896) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Société et al. (1961) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Société et al. (1969) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Société et al. (1977) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stewart et al. (2018) | 1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
inpn@mnhn.fr ">TINGUY Hugues |
1 | 0,07% | 1 | 0,18% | 1 | 0,18% | 1 | 0,18% |
Wegensteiner et al. (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |