Fonge des Antilles françaises
Fungi des Antilles
223 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 | 20,8% | 143 | 8,02% | 143 | 8,39% | 140 | 8,01% |
Courtecuisse (2006) | 615 | 12,36% | 522 | 29,29% | 515 | 30,21% | 517 | 29,59% |
Bricaud (2007) | 444 | 8,92% | 352 | 19,75% | 308 | 18,06% | 347 | 19,86% |
Courtecuisse & Welti (2013) | 387 | 7,78% | 274 | 15,38% | 267 | 15,66% | 268 | 15,34% |
Roux (2012) | 303 | 6,09% | 57 | 3,2% | 56 | 3,28% | 53 | 3,03% |
Øvstedal (2010) | 288 | 5,79% | 252 | 14,14% | 246 | 14,43% | 247 | 14,14% |
Borgato et al. (2020) | 244 | 4,9% | 222 | 12,46% | 220 | 12,9% | 221 | 12,65% |
Elix & McCarthy (1998) | 173 | 3,48% | 133 | 7,46% | 131 | 7,68% | 121 | 6,93% |
Courtecuisse et al. (1996) | 139 | 2,79% | 103 | 5,78% | 102 | 5,98% | 98 | 5,61% |
Bricaud (2009) | 125 | 2,51% | 121 | 6,79% | 119 | 6,98% | 118 | 6,75% |
Jaouen et al. (2019) | 115 | 2,31% | 89 | 4,99% | 89 | 5,22% | 85 | 4,87% |
Hekking & Sipman (1988) | 104 | 2,09% | 77 | 4,32% | 75 | 4,4% | 71 | 4,06% |
Boom et al. (2011) | 99 | 1,99% | 87 | 4,88% | 87 | 5,1% | 82 | 4,69% |
Lücking (2006) | 95 | 1,91% | 90 | 5,05% | 90 | 5,28% | 87 | 4,98% |
Duss (1903) | 81 | 1,63% | 77 | 4,32% | 77 | 4,52% | 77 | 4,41% |
Horak & Mouchacca (1998) | 76 | 1,53% | 27 | 1,52% | 27 | 1,58% | 25 | 1,43% |
Bricaud (2008) | 65 | 1,31% | 57 | 3,2% | 56 | 3,28% | 56 | 3,21% |
Fournier et al. (2016) | 61 | 1,23% | 61 | 3,42% | 58 | 3,4% | 61 | 3,49% |
Imshaug (2019) | 59 | 1,19% | 46 | 2,58% | 46 | 2,7% | 45 | 2,58% |
Buyck (2013) | 57 | 1,15% | 47 | 2,64% | 47 | 2,76% | 44 | 2,52% |
Fournier et al. (2020) | 51 | 1,03% | 51 | 2,86% | 45 | 2,64% | 42 | 2,4% |
Fournier et al. (2017) | 45 | 0,9% | 45 | 2,53% | 45 | 2,64% | 45 | 2,58% |
Roux & Coll (2020) | 38 | 0,76% | 15 | 0,84% | 15 | 0,88% | 15 | 0,86% |
Lécuru & Courtecuisse (2013) | 35 | 0,7% | 33 | 1,85% | 33 | 1,94% | 33 | 1,89% |
Fournier et al. (2017) | 29 | 0,58% | 29 | 1,63% | 26 | 1,52% | 29 | 1,66% |
Fournier et al. (2018) | 29 | 0,58% | 29 | 1,63% | 28 | 1,64% | 29 | 1,66% |
Aptroot & Lücking (2016) | 26 | 0,52% | 26 | 1,46% | 26 | 1,52% | 26 | 1,49% |
Corriol & Roy (2021) | 26 | 0,52% | 20 | 1,12% | 20 | 1,17% | 20 | 1,14% |
Fournier et al. (2019) | 26 | 0,52% | 23 | 1,29% | 23 | 1,35% | 23 | 1,32% |
Fournier et al. (2017) | 25 | 0,5% | 25 | 1,4% | 18 | 1,06% | 21 | 1,2% |
Jabiol & Labeille (2022) | 25 | 0,5% | 23 | 1,29% | 23 | 1,35% | 23 | 1,32% |
Abraham (2021) | 23 | 0,46% | 22 | 1,23% | 22 | 1,29% | 22 | 1,26% |
Fournier et al. (2024) | 20 | 0,4% | 20 | 1,12% | 20 | 1,17% | 20 | 1,14% |
Kohlmeyer (1981) | 20 | 0,4% | 13 | 0,73% | 13 | 0,76% | 13 | 0,74% |
Lebreton (2017) | 16 | 0,32% | 13 | 0,73% | 13 | 0,76% | 13 | 0,74% |
Rivoire (2018) | 16 | 0,32% | 12 | 0,67% | 12 | 0,7% | 12 | 0,69% |
Delgat et al. (2020) | 13 | 0,26% | 13 | 0,73% | 13 | 0,76% | 13 | 0,74% |
Aptroot et al. (2011) | 12 | 0,24% | 11 | 0,62% | 11 | 0,65% | 10 | 0,57% |
Braun et al. (2014) | 11 | 0,22% | 11 | 0,62% | 11 | 0,65% | 11 | 0,63% |
Fournier & Lechat (2015) | 11 | 0,22% | 11 | 0,62% | 11 | 0,65% | 11 | 0,63% |
Questel (2022) | 11 | 0,22% | 10 | 0,56% | 10 | 0,59% | 10 | 0,57% |
Abraham (2010) | 10 | 0,2% | 9 | 0,51% | 9 | 0,53% | 9 | 0,52% |
Accioly et al. (2019) | 10 | 0,2% | 10 | 0,56% | 10 | 0,59% | 10 | 0,57% |
Chauvet (1991) | 10 | 0,2% | 10 | 0,56% | 10 | 0,59% | 10 | 0,57% |
Lücking & Kalb (2018) | 10 | 0,2% | 9 | 0,51% | 9 | 0,53% | 9 | 0,52% |
Fournier et al. (2016) | 9 | 0,18% | 9 | 0,51% | 9 | 0,53% | 9 | 0,52% |
Gruhn & Rödel (2020) | 9 | 0,18% | 9 | 0,51% | 9 | 0,53% | 9 | 0,52% |
Volkmann-Kohlmeyer & Kohlmeyer (1993) | 9 | 0,18% | 7 | 0,39% | 7 | 0,41% | 7 | 0,4% |
Corriol & Hannoire (2018) | 8 | 0,16% | 6 | 0,34% | 6 | 0,35% | 6 | 0,34% |
Fournier & Lechat (2016) | 8 | 0,16% | 8 | 0,45% | 8 | 0,47% | 8 | 0,46% |
Gruhn et al. (2017) | 8 | 0,16% | 8 | 0,45% | 8 | 0,47% | 8 | 0,46% |
Jabiol et al. (2013) | 8 | 0,16% | 8 | 0,45% | 8 | 0,47% | 8 | 0,46% |
Louwhoff & Elix (2002) | 8 | 0,16% | 8 | 0,45% | 8 | 0,47% | 8 | 0,46% |
Vainio (1915) | 8 | 0,16% | 4 | 0,22% | 0 | 0% | 4 | 0,23% |
European Nucleotide Archive (2019) | 7 | 0,14% | 7 | 0,39% | 7 | 0,41% | 7 | 0,4% |
Kuhnert et al. (2013) | 7 | 0,14% | 5 | 0,28% | 5 | 0,29% | 5 | 0,29% |
Le Gallo (1952) | 7 | 0,14% | 5 | 0,28% | 5 | 0,29% | 5 | 0,29% |
Xavier-leite et al. (2023) | 7 | 0,14% | 7 | 0,39% | 7 | 0,41% | 7 | 0,4% |
Lechat & Fournier (2013) | 6 | 0,12% | 6 | 0,34% | 6 | 0,35% | 6 | 0,34% |
Miersch & Rödel (2014) | 6 | 0,12% | 6 | 0,34% | 6 | 0,35% | 6 | 0,34% |
Patouillard (1900) | 6 | 0,12% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Roux et al. (2022) | 6 | 0,12% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Sherwood (1974) | 6 | 0,12% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Zaremski et al. (2014) | 6 | 0,12% | 6 | 0,34% | 6 | 0,35% | 6 | 0,34% |
Fournier et al. (2014) | 5 | 0,1% | 5 | 0,28% | 5 | 0,29% | 5 | 0,29% |
Gruhn et al. (2018) | 5 | 0,1% | 5 | 0,28% | 5 | 0,29% | 5 | 0,29% |
Lechat & Fournier (2019) | 5 | 0,1% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Rogers et al. (2006) | 5 | 0,1% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Berrin et al. (2012) | 4 | 0,08% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Hypoxylon pulicicidum sp nov., a pantropical insecticide-producing endophyte. Plos One, 7(10) : 1-19.">Bills et al. (2012) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Buyck et al. (2016) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Comstock & Bailey (2000) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Elix (2009) | 4 | 0,08% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Gruhn et al. (2015) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Hale (1973) | 4 | 0,08% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Lechat & Courtecuisse (2010) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Lechat et al. (2010) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Lécuru et al. (2013) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Lücking et al. (2013) | 4 | 0,08% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Moreau et al. (2023) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Øvstedal & Elix (2007) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Roux (2013) | 4 | 0,08% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Samuels et al. (2006) | 4 | 0,08% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Sutton & Waterston (1964) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
The International Barcode of Life Consortium (2016) | 4 | 0,08% | 4 | 0,22% | 4 | 0,23% | 4 | 0,23% |
Vainio (1899) | 4 | 0,08% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Welti & Courtecuisse (2010) | 4 | 0,08% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Zhang et al. (2015) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Armada (2018) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Borgato & Ertz (2018) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Cheype (2015) | 3 | 0,06% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Crous et al. (2020) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Ephytia (2020) | 3 | 0,06% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Gruhn et al. (2016) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Gruhn et al. (2017) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Hernández-Restrepo et al. (2022) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Herrera et al. (2015) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Langeron (1928) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lechat & Fournier (2015) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Lechat & Fournier (2016) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Lechat & Fournier (2017) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Lechat et al. (2015) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Lücking (2015) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Masson et al. (2024) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Mongkolsuk et al. (2015) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
O’Donnell et al. (2022) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Riebesehl et al. (2019) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Rivoire (2013) | 3 | 0,06% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Rogers et al. (2007) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Van et al. (2016) | 3 | 0,06% | 3 | 0,17% | 3 | 0,18% | 3 | 0,17% |
Antonín & Noordeloos (2004) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Aptroot et al. (2008) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Aveskamp et al. (2010) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Balazuc (1978) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Baral et al. (2020) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Boidin & Gilles (1986) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Boidin & Gilles (2000) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Boidin et al. (1987) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Boidin et al. (1988) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Bon (1999) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Corriol (2009) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Crous et al. (2019) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Delpont (2019) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dop (1905) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ertz & Lebreton (2024) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Feuerstein et al. (2022) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Fournier et al. (2015) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Fournier (2022) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Fritz-Sheridan & Portecop (1987) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Gerasimova et al. (2021) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Giraldo & Crous (2019) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Gruhn & Rivoire (2016) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Guzmán et al. (2003) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Jaklitsch et al. (2015) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Kistenich et al. (2018) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Kohlmeyer & Volkmann-Kohlmeyer (1998) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Kondratyuk et al. (2020) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lebreton & Aptroot (2020) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Lechat & Fournier (2020) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Looney et al. (2013) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lücking et al. (2009) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Medeiros et al. (2017) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Moncada et al. (2018) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Nakasone (2015) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ortiz-santana et al. (2021) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Otálora et al. (2013) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Øvstedal & Elix (2010) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Patouillard (1902) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Petrini & Petrini (2012) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Redecker et al. (2007) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rogers & Ju (1998) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Sérusiaux & Coppins (2009) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Sherwood (1977) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Sydow & Sydow (1920) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Turcati (2019) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Valade & Moreau (2022) | 2 | 0,04% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Van Vooren & Lopez (2020) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Verbeken et al. (2012) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Vezda & Vivant (1992) | 2 | 0,04% | 2 | 0,11% | 2 | 0,12% | 2 | 0,11% |
Allain & Goodman (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Anonyme (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aptroot et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Arup et al. (2013) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Beller (1971) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand & Roux (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Blanco-dios (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Boidin & Gilles (1988) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Boidin & Gilles (1988) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Boidin & Gilles (1989) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Braun et al. (1999) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bungartz et al. (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Chauvet (1990) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Chaverri et al. (2008) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Chen et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Chen et al. (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Cheype (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Clauzade & Roux (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coimbra et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Cooper (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dai (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Dejean et al. (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Dennis (1954) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ertz et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Fouillaud et al. (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Fournier & Lechat (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Frisch et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Frisch (2006) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Goffinet (1992) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Gruhn et al. (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hairaud & Chautrand (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hongsanan et al. (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Kuhnert et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lechat & Fournier (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lendemer & Harris (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Longcore et al. (1999) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lowe et al. (2007) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lücking et al. (2005) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lücking et al. (2005) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lücking et al. (2006) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Martin-sans (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Masson & Bauvet (2021) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Masson et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Montagne (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz (2005) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Parnmen et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Pée-laby (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pée-laby (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfister (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Réblová et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivas et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Rivoire (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Rodrigues et al. (2021) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Roux & coll. (2017) | 1 | 0,02% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Roux et al. (2006) | 1 | 0,02% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Roy et al. (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Schmitt et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Sipman et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
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 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Streito et al. (2007) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Vacher et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Yang et al. (2021) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |