Fonge (hors lichens) des Antilles françaises
162 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) | 1031 | 27,41% | 143 | 11,89% | 143 | 12,11% | 140 | 11,81% |
Courtecuisse (2006) | 615 | 16,35% | 522 | 43,39% | 515 | 43,61% | 517 | 43,63% |
Courtecuisse & Welti (2013) | 379 | 10,07% | 267 | 22,19% | 261 | 22,1% | 261 | 22,03% |
Courtecuisse et al. (1996) | 155 | 4,12% | 114 | 9,48% | 113 | 9,57% | 109 | 9,2% |
Duss (1903) | 155 | 4,12% | 88 | 7,32% | 88 | 7,45% | 88 | 7,43% |
Jaouen et al. (2019) | 115 | 3,06% | 89 | 7,4% | 89 | 7,54% | 85 | 7,17% |
Horak & Mouchacca (1998) | 76 | 2,02% | 27 | 2,24% | 27 | 2,29% | 25 | 2,11% |
Fournier et al. (2016) | 61 | 1,62% | 59 | 4,9% | 56 | 4,74% | 59 | 4,98% |
Buyck (2013) | 60 | 1,59% | 50 | 4,16% | 50 | 4,23% | 47 | 3,97% |
Fournier et al. (2020) | 51 | 1,36% | 51 | 4,24% | 45 | 3,81% | 42 | 3,54% |
Fournier et al. (2017) | 45 | 1,2% | 45 | 3,74% | 45 | 3,81% | 45 | 3,8% |
Lécuru & Courtecuisse (2013) | 35 | 0,93% | 33 | 2,74% | 33 | 2,79% | 33 | 2,78% |
Fournier et al. (2017) | 29 | 0,77% | 29 | 2,41% | 26 | 2,2% | 29 | 2,45% |
Fournier et al. (2018) | 29 | 0,77% | 29 | 2,41% | 28 | 2,37% | 29 | 2,45% |
Corriol & Roy (2021) | 28 | 0,74% | 22 | 1,83% | 22 | 1,86% | 22 | 1,86% |
Fournier et al. (2019) | 26 | 0,69% | 23 | 1,91% | 23 | 1,95% | 23 | 1,94% |
Fournier et al. (2017) | 25 | 0,66% | 25 | 2,08% | 18 | 1,52% | 21 | 1,77% |
Jabiol & Labeille (2022) | 25 | 0,66% | 23 | 1,91% | 23 | 1,95% | 23 | 1,94% |
Abraham (2021) | 24 | 0,64% | 22 | 1,83% | 22 | 1,86% | 22 | 1,86% |
Fournier et al. (2024) | 22 | 0,58% | 22 | 1,83% | 22 | 1,86% | 22 | 1,86% |
Kohlmeyer (1981) | 20 | 0,53% | 13 | 1,08% | 13 | 1,1% | 13 | 1,1% |
Rivoire (2018) | 16 | 0,43% | 12 | 1% | 12 | 1,02% | 12 | 1,01% |
Delgat et al. (2020) | 15 | 0,4% | 15 | 1,25% | 15 | 1,27% | 15 | 1,27% |
Fournier & Lechat (2015) | 14 | 0,37% | 14 | 1,16% | 14 | 1,19% | 14 | 1,18% |
Braun et al. (2014) | 11 | 0,29% | 11 | 0,91% | 11 | 0,93% | 11 | 0,93% |
Questel (2022) | 11 | 0,29% | 10 | 0,83% | 10 | 0,85% | 10 | 0,84% |
Accioly et al. (2019) | 10 | 0,27% | 10 | 0,83% | 10 | 0,85% | 10 | 0,84% |
Chauvet (1991) | 10 | 0,27% | 10 | 0,83% | 10 | 0,85% | 10 | 0,84% |
Fournier et al. (2016) | 9 | 0,24% | 9 | 0,75% | 9 | 0,76% | 9 | 0,76% |
Gruhn & Rödel (2020) | 9 | 0,24% | 9 | 0,75% | 9 | 0,76% | 9 | 0,76% |
Volkmann-Kohlmeyer & Kohlmeyer (1993) | 9 | 0,24% | 7 | 0,58% | 7 | 0,59% | 7 | 0,59% |
Fournier & Lechat (2016) | 8 | 0,21% | 8 | 0,67% | 8 | 0,68% | 8 | 0,68% |
Gruhn et al. (2017) | 8 | 0,21% | 8 | 0,67% | 8 | 0,68% | 8 | 0,68% |
Jabiol et al. (2013) | 8 | 0,21% | 8 | 0,67% | 8 | 0,68% | 8 | 0,68% |
Corriol & Hannoire (2018) | 7 | 0,19% | 6 | 0,5% | 6 | 0,51% | 6 | 0,51% |
European Nucleotide Archive (2019) | 7 | 0,19% | 7 | 0,58% | 7 | 0,59% | 7 | 0,59% |
Kuhnert et al. (2013) | 7 | 0,19% | 5 | 0,42% | 5 | 0,42% | 5 | 0,42% |
Aptroot & Lücking (2016) | 6 | 0,16% | 6 | 0,5% | 6 | 0,51% | 6 | 0,51% |
Lechat & Fournier (2013) | 6 | 0,16% | 6 | 0,5% | 6 | 0,51% | 6 | 0,51% |
Miersch & Rödel (2014) | 6 | 0,16% | 6 | 0,5% | 6 | 0,51% | 6 | 0,51% |
Patouillard (1900) | 6 | 0,16% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Sherwood (1974) | 6 | 0,16% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Zaremski et al. (2014) | 6 | 0,16% | 6 | 0,5% | 6 | 0,51% | 6 | 0,51% |
Fournier et al. (2014) | 5 | 0,13% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Gruhn et al. (2018) | 5 | 0,13% | 5 | 0,42% | 5 | 0,42% | 5 | 0,42% |
Lechat & Fournier (2019) | 5 | 0,13% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Rogers & Ju (1998) | 5 | 0,13% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Rogers et al. (2006) | 5 | 0,13% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Berrin et al. (2012) | 4 | 0,11% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Hypoxylon pulicicidum sp nov., a pantropical insecticide-producing endophyte. Plos One, 7(10) : 1-19.">Bills et al. (2012) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Borgato et al. (2020) | 4 | 0,11% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Buyck et al. (2016) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Comstock & Bailey (2000) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Gruhn et al. (2015) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Hale (1973) | 4 | 0,11% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Lechat & Courtecuisse (2010) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Lechat et al. (2010) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Lécuru et al. (2013) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Moreau et al. (2023) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Samuels et al. (2006) | 4 | 0,11% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Sutton & Waterston (1964) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
The International Barcode of Life Consortium (2016) | 4 | 0,11% | 4 | 0,33% | 4 | 0,34% | 4 | 0,34% |
Welti & Courtecuisse (2010) | 4 | 0,11% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Zhang et al. (2015) | 4 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Armada (2018) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Braun et al. (1999) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Cheype (2015) | 3 | 0,08% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Crous et al. (2020) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Ephytia (2020) | 3 | 0,08% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Gruhn et al. (2016) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Gruhn et al. (2017) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Hernández-Restrepo et al. (2022) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Herrera et al. (2015) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Imshaug (2019) | 3 | 0,08% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Langeron (1928) | 3 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lechat & Fournier (2015) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Lechat & Fournier (2016) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Lechat & Fournier (2017) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Lechat et al. (2015) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
O’Donnell et al. (2022) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Riebesehl et al. (2019) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Rivoire (2013) | 3 | 0,08% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Rogers et al. (2007) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Van et al. (2016) | 3 | 0,08% | 3 | 0,25% | 3 | 0,25% | 3 | 0,25% |
Antonín & Noordeloos (2004) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Aveskamp et al. (2010) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Balazuc (1978) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Baral et al. (2014) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Baral et al. (2020) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Boidin & Gilles (1986) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Boidin & Gilles (2000) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Boidin et al. (1987) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Boidin et al. (1988) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Bon (1999) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chaverri et al. (2008) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Corriol (2009) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Crous et al. (2019) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Delpont (2019) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dop (1905) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier et al. (2015) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Fournier (2022) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Giraldo & Crous (2019) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Gruhn & Rivoire (2016) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Guzmán et al. (2003) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Hariot & Patouillard (1903) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jaklitsch et al. (2015) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Kohlmeyer & Volkmann-Kohlmeyer (1998) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Lechat & Fournier (2020) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Looney et al. (2013) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Lücking (2015) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Nakasone (2015) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Ortiz-santana et al. (2021) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Patouillard (1902) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Petrini & Petrini (2012) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Redecker et al. (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherwood (1977) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Sydow & Sydow (1920) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Vainio (1915) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Valade & Moreau (2022) | 2 | 0,05% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Van Vooren & Lopez (2020) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Verbeken et al. (2012) | 2 | 0,05% | 2 | 0,17% | 2 | 0,17% | 2 | 0,17% |
Allain & Goodman (2017) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
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 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Boidin & Gilles (1988) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Boidin & Gilles (1988) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Boidin & Gilles (1989) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Carbone & Rubini (2024) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Chauvet (1990) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Chen et al. (2017) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Cheype (2010) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Coimbra et al. (2015) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Cooper (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dai (2010) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Dejean et al. (2010) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Dennis (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dennis (1954) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fouillaud et al. (2017) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Fournier & Lechat (2015) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Gruhn et al. (2017) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Hairaud & Chautrand (2017) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Hudson et al. (2021) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Kuhnert et al. (2015) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Lechat & Fournier (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Longcore et al. (1999) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Lowe et al. (2007) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
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 | 0,08% | 1 | 0,08% | 1 | 0,08% |
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 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Roy et al. (2016) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
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 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Streito et al. (2007) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Vacher et al. (2014) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |
Yang et al. (2021) | 1 | 0,03% | 1 | 0,08% | 1 | 0,08% | 1 | 0,08% |