Ascomycètes de Nouvelle-Calédonie
Ascomycota de Nouvelle-Calédonie
100 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) | 706 | 38,33% | 622 | 74,58% | 562 | 73,08% | 584 | 74,02% |
Roux (2012) | 455 | 24,7% | 83 | 9,95% | 81 | 10,53% | 73 | 9,25% |
Boom et al. (2011) | 99 | 5,37% | 94 | 11,27% | 94 | 12,22% | 90 | 11,41% |
Hekking & Sipman (1988) | 77 | 4,18% | 62 | 7,43% | 61 | 7,93% | 55 | 6,97% |
Bricaud (2007) | 66 | 3,58% | 51 | 6,12% | 50 | 6,5% | 44 | 5,58% |
Braun et al. (1999) | 65 | 3,53% | 62 | 7,43% | 61 | 7,93% | 60 | 7,6% |
Borgato et al. (2020) | 55 | 2,99% | 48 | 5,76% | 48 | 6,24% | 43 | 5,45% |
Huguenin (1969) | 49 | 2,66% | 43 | 5,16% | 41 | 5,33% | 43 | 5,45% |
Papong et al. (2014) | 47 | 2,55% | 45 | 5,4% | 45 | 5,85% | 45 | 5,7% |
Louwhoff & Elix (2002) | 41 | 2,23% | 40 | 4,8% | 40 | 5,2% | 40 | 5,07% |
Roux & Coll (2020) | 36 | 1,95% | 12 | 1,44% | 12 | 1,56% | 12 | 1,52% |
Aptroot & Lücking (2016) | 30 | 1,63% | 29 | 3,48% | 29 | 3,77% | 29 | 3,68% |
Aptroot et al. (2011) | 23 | 1,25% | 20 | 2,4% | 20 | 2,6% | 18 | 2,28% |
Imshaug (2019) | 19 | 1,03% | 15 | 1,8% | 15 | 1,95% | 14 | 1,77% |
Abraham (2010) | 16 | 0,87% | 15 | 1,8% | 15 | 1,95% | 11 | 1,39% |
Aptroot (2014) | 15 | 0,81% | 15 | 1,8% | 15 | 1,95% | 15 | 1,9% |
Braun et al. (2014) | 15 | 0,81% | 15 | 1,8% | 15 | 1,95% | 15 | 1,9% |
Le Gallo (1952) | 14 | 0,76% | 9 | 1,08% | 9 | 1,17% | 5 | 0,63% |
Lücking (2006) | 14 | 0,76% | 13 | 1,56% | 13 | 1,69% | 12 | 1,52% |
Huguenin (1969) | 12 | 0,65% | 12 | 1,44% | 12 | 1,56% | 12 | 1,52% |
Bricaud (2009) | 11 | 0,6% | 11 | 1,32% | 11 | 1,43% | 10 | 1,27% |
Elix (2009) | 9 | 0,49% | 8 | 0,96% | 8 | 1,04% | 8 | 1,01% |
Lücking & Kalb (2001) | 8 | 0,43% | 8 | 0,96% | 8 | 1,04% | 8 | 1,01% |
Anonyme (2018) | 7 | 0,38% | 4 | 0,48% | 4 | 0,52% | 4 | 0,51% |
Rogers & Ju (1998) | 7 | 0,38% | 4 | 0,48% | 4 | 0,52% | 4 | 0,51% |
Elvebakk et al. (2016) | 6 | 0,33% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Kistenich et al. (2018) | 6 | 0,33% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Lebreton (2017) | 6 | 0,33% | 6 | 0,72% | 6 | 0,78% | 6 | 0,76% |
Roux (2013) | 6 | 0,33% | 4 | 0,48% | 4 | 0,52% | 3 | 0,38% |
Jorgensen & Gjerde (2012) | 5 | 0,27% | 5 | 0,6% | 5 | 0,65% | 5 | 0,63% |
Roux & Coll (2023) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearson et al. (1922) | 4 | 0,22% | 4 | 0,48% | 4 | 0,52% | 4 | 0,51% |
Roux & coll (2022) | 4 | 0,22% | 1 | 0,12% | 1 | 0,13% | 1 | 0,13% |
Udagawa et al. (1994) | 4 | 0,22% | 4 | 0,48% | 4 | 0,52% | 4 | 0,51% |
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 (1964) | 2 | 0,11% | 2 | 0,24% | 2 | 0,26% | 2 | 0,25% |
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% |
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% |
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% |
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% |
Zhao et al. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |