Basidiomycètes de Nouvelle-Calédonie
Basidiomycota de Nouvelle-Calédonie
66 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 | 35,54% | 62 | 17,66% | 62 | 17,97% | 61 | 17,63% |
| Horak & Mouchacca (1998) | 285 | 22,76% | 168 | 47,86% | 164 | 47,54% | 168 | 48,55% |
| Courtecuisse & Welti (2013) | 86 | 6,87% | 52 | 14,81% | 52 | 15,07% | 52 | 15,03% |
| Mouchacca & Horak (1998) | 67 | 5,35% | 62 | 17,66% | 60 | 17,39% | 61 | 17,63% |
| Courtecuisse et al. (1996) | 35 | 2,8% | 25 | 7,12% | 25 | 7,25% | 25 | 7,23% |
| Buyck (2013) | 25 | 2% | 20 | 5,7% | 20 | 5,8% | 20 | 5,78% |
| Jaouen et al. (2019) | 21 | 1,68% | 15 | 4,27% | 15 | 4,35% | 15 | 4,34% |
| Courtecuisse (2006) | 17 | 1,36% | 16 | 4,56% | 16 | 4,64% | 16 | 4,62% |
| Eyssartier et al. (2011) | 12 | 0,96% | 12 | 3,42% | 12 | 3,48% | 12 | 3,47% |
| Abraham (2021) | 11 | 0,88% | 10 | 2,85% | 10 | 2,9% | 10 | 2,89% |
| Rivoire (2018) | 9 | 0,72% | 8 | 2,28% | 8 | 2,32% | 8 | 2,31% |
| Buyck et al. (2024) | 6 | 0,48% | 6 | 1,71% | 6 | 1,74% | 6 | 1,73% |
| Lécuru & Courtecuisse (2013) | 6 | 0,48% | 5 | 1,42% | 5 | 1,45% | 5 | 1,45% |
| Berndt (2013) | 5 | 0,4% | 5 | 1,42% | 5 | 1,45% | 5 | 1,45% |
| Buyck (2014) | 5 | 0,4% | 5 | 1,42% | 5 | 1,45% | 5 | 1,45% |
| Corriol & Roy (2021) | 5 | 0,4% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Elix & McCarthy (1998) | 5 | 0,4% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Questel (2022) | 5 | 0,4% | 4 | 1,14% | 4 | 1,16% | 4 | 1,16% |
| Eyssartier et al. (2008) | 4 | 0,32% | 4 | 1,14% | 4 | 1,16% | 4 | 1,16% |
| Lebel et al. (2022) | 4 | 0,32% | 4 | 1,14% | 4 | 1,16% | 4 | 1,16% |
| Buyck et al. (2012) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Ducousso et al. (2004) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Duhem & Buyck (2011) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Duhem & Buyck (2012) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Ephytia (2020) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Eyssartier et al. (2010) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Lebel et al. (2015) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Lebel et al. (2018) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Rivoire (2013) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Ryvarden (2005) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Zaremski et al. (2014) | 3 | 0,24% | 3 | 0,85% | 3 | 0,87% | 3 | 0,87% |
| Armada (2018) | 2 | 0,16% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Berrin et al. (2012) | 2 | 0,16% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Bon (1999) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boom et al. (2011) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borgato et al. (2020) | 2 | 0,16% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Bricaud (2007) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Buyck et al. (2017) | 2 | 0,16% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Buyck (2004) | 2 | 0,16% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Corriol (2009) | 2 | 0,16% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Eyssartier & Ducousso (2017) | 2 | 0,16% | 2 | 0,57% | 2 | 0,58% | 2 | 0,58% |
| Looney et al. (2013) | 2 | 0,16% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Øvstedal (2010) | 2 | 0,16% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Welti & Courtecuisse (2010) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aime & Mctaggart (2021) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Beller (1971) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (1989) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Bricaud (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bricaud (2009) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Buyck et al. (2016) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Chevassut (1992) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 0 | 0% |
| Cheype (2010) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Cooper (2011) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dai (2010) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Leyronas et al. (2004) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Lücking et al. (2013) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lücking (2006) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayor (1928) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noordeloos et al. (2022) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Padamsee & Mckenzie (2012) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
| Pée-laby (1896) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Royaud (1991) | 1 | 0,08% | 1 | 0,28% | 0 | 0% | 1 | 0,29% |
| Société et al. (1961) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1969) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1977) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart et al. (2018) | 1 | 0,08% | 1 | 0,28% | 1 | 0,29% | 1 | 0,29% |
