Fonge (hors lichens) des Antilles françaises
163 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) | 1035 | 29,46% | 143 | 12,5% | 143 | 12,79% | 140 | 12,48% |
Courtecuisse (2006) | 615 | 17,51% | 522 | 45,63% | 515 | 46,06% | 517 | 46,08% |
Courtecuisse & Welti (2013) | 381 | 10,85% | 268 | 23,43% | 262 | 23,43% | 262 | 23,35% |
Courtecuisse et al. (1996) | 139 | 3,96% | 103 | 9% | 102 | 9,12% | 98 | 8,73% |
Jaouen et al. (2019) | 115 | 3,27% | 89 | 7,78% | 89 | 7,96% | 85 | 7,58% |
Horak & Mouchacca (1998) | 76 | 2,16% | 27 | 2,36% | 27 | 2,42% | 25 | 2,23% |
Fournier et al. (2016) | 61 | 1,74% | 61 | 5,33% | 58 | 5,19% | 61 | 5,44% |
Buyck (2013) | 57 | 1,62% | 47 | 4,11% | 47 | 4,2% | 44 | 3,92% |
Bricaud (2007) | 51 | 1,45% | 41 | 3,58% | 38 | 3,4% | 38 | 3,39% |
Fournier et al. (2020) | 51 | 1,45% | 51 | 4,46% | 45 | 4,03% | 42 | 3,74% |
Fournier et al. (2017) | 45 | 1,28% | 45 | 3,93% | 45 | 4,03% | 45 | 4,01% |
Lécuru & Courtecuisse (2013) | 35 | 1% | 33 | 2,88% | 33 | 2,95% | 33 | 2,94% |
Fournier et al. (2017) | 29 | 0,83% | 29 | 2,53% | 26 | 2,33% | 29 | 2,58% |
Fournier et al. (2018) | 29 | 0,83% | 29 | 2,53% | 28 | 2,5% | 29 | 2,58% |
Corriol & Roy (2021) | 26 | 0,74% | 20 | 1,75% | 20 | 1,79% | 20 | 1,78% |
Fournier et al. (2019) | 26 | 0,74% | 23 | 2,01% | 23 | 2,06% | 23 | 2,05% |
Fournier et al. (2017) | 25 | 0,71% | 25 | 2,19% | 18 | 1,61% | 21 | 1,87% |
Jabiol & Labeille (2022) | 25 | 0,71% | 23 | 2,01% | 23 | 2,06% | 23 | 2,05% |
Abraham (2021) | 23 | 0,65% | 22 | 1,92% | 22 | 1,97% | 22 | 1,96% |
Kohlmeyer (1981) | 20 | 0,57% | 13 | 1,14% | 13 | 1,16% | 13 | 1,16% |
Rivoire (2018) | 16 | 0,46% | 12 | 1,05% | 12 | 1,07% | 12 | 1,07% |
Braun et al. (2014) | 11 | 0,31% | 11 | 0,96% | 11 | 0,98% | 11 | 0,98% |
Fournier & Lechat (2015) | 11 | 0,31% | 11 | 0,96% | 11 | 0,98% | 11 | 0,98% |
Questel (2022) | 11 | 0,31% | 10 | 0,87% | 10 | 0,89% | 10 | 0,89% |
Accioly et al. (2019) | 10 | 0,28% | 10 | 0,87% | 10 | 0,89% | 10 | 0,89% |
Chauvet (1991) | 10 | 0,28% | 10 | 0,87% | 10 | 0,89% | 10 | 0,89% |
Fournier et al. (2016) | 9 | 0,26% | 9 | 0,79% | 9 | 0,81% | 9 | 0,8% |
Gruhn & Rödel (2020) | 9 | 0,26% | 9 | 0,79% | 9 | 0,81% | 9 | 0,8% |
Volkmann-Kohlmeyer & Kohlmeyer (1993) | 9 | 0,26% | 7 | 0,61% | 7 | 0,63% | 7 | 0,62% |
Corriol & Hannoire (2018) | 8 | 0,23% | 6 | 0,52% | 6 | 0,54% | 6 | 0,53% |
Fournier & Lechat (2016) | 8 | 0,23% | 8 | 0,7% | 8 | 0,72% | 8 | 0,71% |
Gruhn et al. (2017) | 8 | 0,23% | 8 | 0,7% | 8 | 0,72% | 8 | 0,71% |
Jabiol et al. (2013) | 8 | 0,23% | 8 | 0,7% | 8 | 0,72% | 8 | 0,71% |
Aptroot & Lücking (2016) | 7 | 0,2% | 7 | 0,61% | 7 | 0,63% | 7 | 0,62% |
Borgato et al. (2020) | 7 | 0,2% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
European Nucleotide Archive (2019) | 7 | 0,2% | 7 | 0,61% | 7 | 0,63% | 7 | 0,62% |
Imshaug (2019) | 7 | 0,2% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
Kuhnert et al. (2013) | 7 | 0,2% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
Lechat & Fournier (2013) | 6 | 0,17% | 6 | 0,52% | 6 | 0,54% | 6 | 0,53% |
Miersch & Rödel (2014) | 6 | 0,17% | 6 | 0,52% | 6 | 0,54% | 6 | 0,53% |
Patouillard (1900) | 6 | 0,17% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Sherwood (1974) | 6 | 0,17% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Vainio (1915) | 6 | 0,17% | 4 | 0,35% | 0 | 0% | 4 | 0,36% |
Zaremski et al. (2014) | 6 | 0,17% | 6 | 0,52% | 6 | 0,54% | 6 | 0,53% |
Fournier et al. (2014) | 5 | 0,14% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
Gruhn et al. (2018) | 5 | 0,14% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
Lebreton (2017) | 5 | 0,14% | 5 | 0,44% | 5 | 0,45% | 5 | 0,45% |
Lechat & Fournier (2019) | 5 | 0,14% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Rogers et al. (2006) | 5 | 0,14% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Berrin et al. (2012) | 4 | 0,11% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Hypoxylon pulicicidum sp nov., a pantropical insecticide-producing endophyte. Plos One, 7(10) : 1-19.">Bills et al. (2012) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Buyck et al. (2016) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Gruhn et al. (2015) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Hale (1973) | 4 | 0,11% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Lechat & Courtecuisse (2010) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Lechat et al. (2010) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Lécuru et al. (2013) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Moreau et al. (2023) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Øvstedal & Elix (2007) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Samuels et al. (2006) | 4 | 0,11% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
The International Barcode of Life Consortium (2016) | 4 | 0,11% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Vainio (1899) | 4 | 0,11% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Welti & Courtecuisse (2010) | 4 | 0,11% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Zhang et al. (2015) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Armada (2018) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Cheype (2015) | 3 | 0,09% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Crous et al. (2020) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Elix & McCarthy (1998) | 3 | 0,09% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Ephytia (2020) | 3 | 0,09% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gruhn et al. (2016) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Gruhn et al. (2017) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Hekking & Sipman (1988) | 3 | 0,09% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Hernández-Restrepo et al. (2022) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Herrera et al. (2015) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Langeron (1928) | 3 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lechat & Fournier (2015) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Lechat & Fournier (2016) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Lechat & Fournier (2017) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Lechat et al. (2015) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
O’Donnell et al. (2022) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Riebesehl et al. (2019) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Rivoire (2013) | 3 | 0,09% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Rogers et al. (2007) | 3 | 0,09% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Antonín & Noordeloos (2004) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Aptroot et al. (2008) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Aveskamp et al. (2010) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Balazuc (1978) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Baral et al. (2020) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Boidin & Gilles (1986) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Boidin & Gilles (2000) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Boidin et al. (1987) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Boidin et al. (1988) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Bon (1999) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Corriol (2009) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Crous et al. (2019) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Delgat et al. (2020) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Delpont (2019) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dop (1905) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Duss (1903) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Fournier et al. (2015) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Fournier (2022) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Giraldo & Crous (2019) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gruhn & Rivoire (2016) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Guzmán et al. (2003) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Jaklitsch et al. (2015) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Kohlmeyer & Volkmann-Kohlmeyer (1998) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Lechat & Fournier (2020) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Looney et al. (2013) | 2 | 0,06% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lücking (2015) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Nakasone (2015) | 2 | 0,06% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ortiz-santana et al. (2021) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Øvstedal & Elix (2010) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Patouillard (1902) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Petrini & Petrini (2012) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Redecker et al. (2007) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogers & Ju (1998) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Sérusiaux & Coppins (2009) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Sherwood (1977) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Sydow & Sydow (1920) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Valade & Moreau (2022) | 2 | 0,06% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Van Vooren & Lopez (2020) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Allain & Goodman (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Anonyme (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beller (1971) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanco-dios (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Boidin & Gilles (1988) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Boidin & Gilles (1988) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Boidin & Gilles (1989) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Braun et al. (1999) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Chauvet (1990) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Chen et al. (2018) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Chen et al. (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cheype (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Coimbra et al. (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cooper (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dai (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dejean et al. (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dennis (1954) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Elix (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fouillaud et al. (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fournier & Lechat (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gruhn et al. (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hairaud & Chautrand (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hudson et al. (2021) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kuhnert et al. (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lechat & Fournier (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Longcore et al. (1999) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lowe et al. (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lücking et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin-sans (1933) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagne (1840) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau et al. (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz (2005) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pée-laby (1896) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pée-laby (1896) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfister (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Réblová et al. (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivoire (2020) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Roy et al. (2016) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Peršoh, D. & Fournier, J. 2013. The Xylariaceae as model example for a unified nomenclature following the "One fungus One name" (1F1N) concept. Mycology An International Journal on Fungal Biology, 4(1): 5-21. ">Stadler et al. (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Streito et al. (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vacher et al. (2014) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Yang et al. (2021) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |