Ascomycètes de Nouvelle-Calédonie
Ascomycota de Nouvelle-Calédonie
110 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Elix & McCarthy (1998) | 704 | 37,69% | 616 | 73,6% | 556 | 72,02% | 578 | 72,89% |
Roux (2012) | 452 | 24,2% | 81 | 9,68% | 79 | 10,23% | 71 | 8,95% |
Boom et al. (2011) | 99 | 5,3% | 93 | 11,11% | 93 | 12,05% | 89 | 11,22% |
Hekking & Sipman (1988) | 76 | 4,07% | 60 | 7,17% | 59 | 7,64% | 53 | 6,68% |
Bricaud (2007) | 73 | 3,91% | 51 | 6,09% | 50 | 6,48% | 43 | 5,42% |
Øvstedal (2010) | 68 | 3,64% | 55 | 6,57% | 55 | 7,12% | 47 | 5,93% |
Braun et al. (1999) | 65 | 3,48% | 62 | 7,41% | 61 | 7,9% | 60 | 7,57% |
Borgato et al. (2020) | 55 | 2,94% | 48 | 5,73% | 48 | 6,22% | 43 | 5,42% |
Huguenin (1969) | 49 | 2,62% | 43 | 5,14% | 41 | 5,31% | 43 | 5,42% |
Papong et al. (2014) | 47 | 2,52% | 45 | 5,38% | 45 | 5,83% | 45 | 5,67% |
Louwhoff & Elix (2002) | 41 | 2,19% | 39 | 4,66% | 39 | 5,05% | 39 | 4,92% |
Roux & Coll (2020) | 40 | 2,14% | 15 | 1,79% | 15 | 1,94% | 15 | 1,89% |
Aptroot & Lücking (2016) | 30 | 1,61% | 29 | 3,46% | 29 | 3,76% | 29 | 3,66% |
Bricaud (2008) | 26 | 1,39% | 23 | 2,75% | 23 | 2,98% | 22 | 2,77% |
Aptroot et al. (2011) | 23 | 1,23% | 19 | 2,27% | 19 | 2,46% | 17 | 2,14% |
Imshaug (2019) | 19 | 1,02% | 15 | 1,79% | 15 | 1,94% | 14 | 1,77% |
Abraham (2010) | 16 | 0,86% | 14 | 1,67% | 14 | 1,81% | 10 | 1,26% |
Aptroot (2014) | 15 | 0,8% | 15 | 1,79% | 15 | 1,94% | 15 | 1,89% |
Braun et al. (2014) | 15 | 0,8% | 15 | 1,79% | 15 | 1,94% | 15 | 1,89% |
Le Gallo (1952) | 14 | 0,75% | 8 | 0,96% | 8 | 1,04% | 4 | 0,5% |
Lücking (2006) | 14 | 0,75% | 12 | 1,43% | 12 | 1,55% | 11 | 1,39% |
Huguenin (1969) | 12 | 0,64% | 12 | 1,43% | 12 | 1,55% | 12 | 1,51% |
Bricaud (2009) | 11 | 0,59% | 10 | 1,19% | 10 | 1,3% | 9 | 1,13% |
Elix (2009) | 9 | 0,48% | 8 | 0,96% | 8 | 1,04% | 8 | 1,01% |
Lücking & Kalb (2001) | 8 | 0,43% | 8 | 0,96% | 8 | 1,04% | 8 | 1,01% |
Masson et al. (2024) | 8 | 0,43% | 8 | 0,96% | 8 | 1,04% | 8 | 1,01% |
Anonyme (2018) | 7 | 0,37% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Rogers & Ju (1998) | 7 | 0,37% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Elvebakk et al. (2016) | 6 | 0,32% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Huguenin (1965) | 6 | 0,32% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Kistenich et al. (2018) | 6 | 0,32% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Lebreton (2017) | 6 | 0,32% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Roux (2013) | 6 | 0,32% | 4 | 0,48% | 4 | 0,52% | 3 | 0,38% |
Duss (1903) | 5 | 0,27% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Jorgensen & Gjerde (2012) | 5 | 0,27% | 5 | 0,6% | 5 | 0,65% | 5 | 0,63% |
Roux et al. (2023) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Huguenin (1964) | 4 | 0,21% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Pearson et al. (1922) | 4 | 0,21% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Roux et al. (2022) | 4 | 0,21% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Udagawa et al. (1994) | 4 | 0,21% | 4 | 0,48% | 4 | 0,52% | 4 | 0,5% |
Dupont et al. (2000) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
Hughes et al. (2004) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
Liberato & Barreto (2006) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lücking et al. (2016) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
McTaggart et al. (2008) | 3 | 0,16% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
O’Donnell et al. (2022) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
Rikkinen et al. (2014) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
Rikkinen et al. (2016) | 3 | 0,16% | 3 | 0,36% | 3 | 0,39% | 3 | 0,38% |
Videira et al. (2017) | 3 | 0,16% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Archer & Elix (2009) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Bertrand & Roux (2018) | 2 | 0,11% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Bonati & Petitmengin (1907) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Clauzade & Roux (1985) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Courtecuisse et al. (1996) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Deighton (1974) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Döbbeler & Müller (2018) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Döbbeler (2005) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Elix (2019) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Elvebakk (2007) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Hale (1976) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Hariot & Patouillard (1903) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Heim (1966) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Hennings (1903) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Huguenin (1965) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston et al. (2022) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Joshi et al. (2015) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Kalb & Elix (1998) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kalb et al. (2009) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Kalb (2008) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Kondratyuk et al. (2019) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Kwaśna & Nirenberg (2005) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Lebreton et al. (2023) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Lesdain (1910) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Massee (1901) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Mckenzie & Kuthubutheen (1993) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Mckenzie (1995) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
O’donnell et al. (2004) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Schinz (1920) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Sérusiaux & Lücking (2007) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Simon et al. (2018) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Smith (1965) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Spooner (1985) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Turcati (2019) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Udagawa et al. (1994) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Vouaux (1910) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Wakefield et al. (1916) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Wei et al. (2017) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
Arup et al. (2013) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Buyck et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Buyck (2013) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Dennis (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Flörke (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz-Sheridan & Portecop (1987) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Goffinet (1992) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Hongsanan et al. (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Horak & Mouchacca (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jørgensen et al. (2009) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Jørgensen (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Lebreton et al. (2024) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Liberato et al. (2005) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Magain et al. (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Massé (1982) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Müller (1893) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Schmitt et al. (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Sérusiaux et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
inpn@mnhn.fr ">TINGUY Hugues |
1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Vondrák et al. (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Wegensteiner et al. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Xavier-leite et al. (2023) | 1 | 0,05% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Zhao et al. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |