Fonge (hors lichens) de Nouvelle-Calédonie
126 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) | 445 | 28,9% | 62 | 10,82% | 62 | 10,97% | 61 | 10,76% |
| Horak & Mouchacca (1998) | 286 | 18,57% | 168 | 29,32% | 164 | 29,03% | 168 | 29,63% |
| Courtecuisse & Welti (2013) | 84 | 5,45% | 52 | 9,08% | 52 | 9,2% | 52 | 9,17% |
| Mouchacca & Horak (1998) | 67 | 4,35% | 62 | 10,82% | 60 | 10,62% | 61 | 10,76% |
| Braun et al. (1999) | 65 | 4,22% | 62 | 10,82% | 61 | 10,8% | 60 | 10,58% |
| Huguenin (1969) | 49 | 3,18% | 43 | 7,5% | 41 | 7,26% | 43 | 7,58% |
| Papong et al. (2014) | 42 | 2,73% | 40 | 6,98% | 40 | 7,08% | 40 | 7,05% |
| Courtecuisse et al. (1996) | 37 | 2,4% | 27 | 4,71% | 27 | 4,78% | 27 | 4,76% |
| Buyck (2013) | 26 | 1,69% | 21 | 3,66% | 21 | 3,72% | 21 | 3,7% |
| Jaouen et al. (2019) | 21 | 1,36% | 15 | 2,62% | 15 | 2,65% | 15 | 2,65% |
| Louwhoff & Elix (2002) | 20 | 1,3% | 20 | 3,49% | 20 | 3,54% | 20 | 3,53% |
| Courtecuisse (2006) | 17 | 1,1% | 16 | 2,79% | 16 | 2,83% | 16 | 2,82% |
| Aptroot (2014) | 15 | 0,97% | 15 | 2,62% | 15 | 2,65% | 15 | 2,65% |
| Braun et al. (2014) | 15 | 0,97% | 15 | 2,62% | 15 | 2,65% | 15 | 2,65% |
| Crossay et al. (2018) | 12 | 0,78% | 9 | 1,57% | 9 | 1,59% | 9 | 1,59% |
| Eyssartier et al. (2011) | 12 | 0,78% | 12 | 2,09% | 12 | 2,12% | 12 | 2,12% |
| Huguenin (1969) | 12 | 0,78% | 12 | 2,09% | 12 | 2,12% | 12 | 2,12% |
| Abraham (2021) | 11 | 0,71% | 10 | 1,75% | 10 | 1,77% | 10 | 1,76% |
| Aptroot & Lücking (2016) | 11 | 0,71% | 11 | 1,92% | 11 | 1,95% | 11 | 1,94% |
| Rivoire (2018) | 9 | 0,58% | 8 | 1,4% | 8 | 1,42% | 8 | 1,41% |
| Anonyme (2018) | 7 | 0,45% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Rogers & Ju (1998) | 7 | 0,45% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Buyck et al. (2024) | 6 | 0,39% | 6 | 1,05% | 6 | 1,06% | 6 | 1,06% |
| Duss (1903) | 6 | 0,39% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Elvebakk et al. (2016) | 6 | 0,39% | 6 | 1,05% | 6 | 1,06% | 6 | 1,06% |
| Huguenin (1965) | 6 | 0,39% | 6 | 1,05% | 6 | 1,06% | 6 | 1,06% |
| Kistenich et al. (2018) | 6 | 0,39% | 6 | 1,05% | 6 | 1,06% | 6 | 1,06% |
| Lécuru & Courtecuisse (2013) | 6 | 0,39% | 5 | 0,87% | 5 | 0,88% | 5 | 0,88% |
| Lücking & Kalb (2001) | 6 | 0,39% | 6 | 1,05% | 6 | 1,06% | 6 | 1,06% |
| Berndt (2013) | 5 | 0,32% | 5 | 0,87% | 5 | 0,88% | 5 | 0,88% |
| Buyck (2014) | 5 | 0,32% | 5 | 0,87% | 5 | 0,88% | 5 | 0,88% |
| Corriol & Roy (2021) | 5 | 0,32% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Jorgensen & Gjerde (2012) | 5 | 0,32% | 5 | 0,87% | 5 | 0,88% | 5 | 0,88% |
| Questel (2022) | 5 | 0,32% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Comstock & Bailey (2000) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Crossay et al. (2024) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Eyssartier et al. (2008) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Huguenin (1964) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Lebel et al. (2022) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Pearson et al. (1922) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Sutton & Waterston (1964) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Udagawa et al. (1994) | 4 | 0,26% | 4 | 0,7% | 4 | 0,71% | 4 | 0,71% |
| Buyck et al. (2012) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Ducousso et al. (2004) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Duhem & Buyck (2011) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Duhem & Buyck (2012) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Dupont et al. (2000) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Ephytia (2020) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Eyssartier et al. (2010) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Hughes et al. (2004) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Lebel et al. (2015) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Lebel et al. (2018) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Liberato & Barreto (2006) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lücking et al. (2016) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| McTaggart et al. (2008) | 3 | 0,19% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| O’Donnell et al. (2022) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Rikkinen et al. (2014) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Rikkinen et al. (2016) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Rivoire (2013) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Ryvarden (2005) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Videira et al. (2017) | 3 | 0,19% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Zaremski et al. (2014) | 3 | 0,19% | 3 | 0,52% | 3 | 0,53% | 3 | 0,53% |
| Archer & Elix (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Armada (2018) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Berrin et al. (2012) | 2 | 0,13% | 1 | 0,17% | 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 | 0,35% | 2 | 0,35% |
| Buyck et al. (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Buyck (2004) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Corriol (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Deighton (1974) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Döbbeler & Müller (2018) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Döbbeler (2005) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Elix (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Elix (2019) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Elvebakk (2007) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Eyssartier & Ducousso (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Hale (1976) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Hariot & Patouillard (1903) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heim (1966) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Hennings (1903) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Huguenin (1965) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnston et al. (2022) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Kalb et al. (2009) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Kalb (2008) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Kwaśna & Nirenberg (2005) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Looney et al. (2013) | 2 | 0,13% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Massee (1901) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Mckenzie & Kuthubutheen (1993) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Mckenzie (1995) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| O’donnell et al. (2004) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Schinz (1920) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Smith (1965) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Spooner (1985) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Udagawa et al. (1994) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Vouaux (1910) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Wakefield et al. (1916) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Wei et al. (2017) | 2 | 0,13% | 2 | 0,35% | 2 | 0,35% | 2 | 0,35% |
| Welti & Courtecuisse (2010) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aime & Mctaggart (2021) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Błaszkowski et al. (2017) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Błaszkowski et al. (2021) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Beller (1971) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (1989) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Buyck et al. (2016) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Chevassut (1992) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 0 | 0% |
| Cheype (2010) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Cooper (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dai (2010) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Dennis (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ehc (1991) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Elix & McCarthy (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kalb & Elix (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leyronas et al. (2004) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Liberato et al. (2005) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Mayor (1928) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noordeloos et al. (2022) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Padamsee & Mckenzie (2012) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Pée-laby (1896) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Royaud (1991) | 1 | 0,06% | 1 | 0,17% | 0 | 0% | 1 | 0,18% |
| Société et al. (1961) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1969) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart et al. (2018) | 1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| inpn@mnhn.fr ">TINGUY Hugues |
1 | 0,06% | 1 | 0,17% | 1 | 0,18% | 1 | 0,18% |
| Wegensteiner et al. (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
