Fonge (hors lichens) de la Réunion
105 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) | 145 | 28,21% | 29 | 9,76% | 28 | 9,52% | 27 | 9,18% |
| Crous et al. (2016) | 36 | 7% | 30 | 10,1% | 30 | 10,2% | 30 | 10,2% |
| Boidin & Gilles (1991) | 30 | 5,84% | 22 | 7,41% | 22 | 7,48% | 22 | 7,48% |
| Boidin & Gilles (2000) | 27 | 5,25% | 27 | 9,09% | 27 | 9,18% | 27 | 9,18% |
| Brand et al. (2014) | 27 | 5,25% | 27 | 9,09% | 27 | 9,18% | 27 | 9,18% |
| Fouillaud et al. (2017) | 24 | 4,67% | 19 | 6,4% | 19 | 6,46% | 19 | 6,46% |
| Mgnify (2018) | 20 | 3,89% | 16 | 5,39% | 16 | 5,44% | 16 | 5,44% |
| Noordeloos & Hausknecht (2007) | 20 | 3,89% | 20 | 6,73% | 20 | 6,8% | 20 | 6,8% |
| Boidin & Gilles (1998) | 18 | 3,5% | 12 | 4,04% | 12 | 4,08% | 12 | 4,08% |
| Boidin et al. (1988) | 17 | 3,31% | 17 | 5,72% | 13 | 4,42% | 16 | 5,44% |
| Leger & Lanquetin (1986) | 17 | 3,31% | 17 | 5,72% | 17 | 5,78% | 17 | 5,78% |
| Boidin & Gilles (1989) | 15 | 2,92% | 14 | 4,71% | 14 | 4,76% | 14 | 4,76% |
| Crous et al. (2015) | 15 | 2,92% | 15 | 5,05% | 15 | 5,1% | 15 | 5,1% |
| Boidin & Gilles (1988) | 14 | 2,72% | 14 | 4,71% | 14 | 4,76% | 14 | 4,76% |
| Boidin et al. (1987) | 14 | 2,72% | 14 | 4,71% | 11 | 3,74% | 13 | 4,42% |
| Courtecuisse & Welti (2013) | 14 | 2,72% | 13 | 4,38% | 13 | 4,42% | 10 | 3,4% |
| Buyck (2013) | 13 | 2,53% | 12 | 4,04% | 12 | 4,08% | 11 | 3,74% |
| Boidin & Gilles (1989) | 12 | 2,33% | 12 | 4,04% | 12 | 4,08% | 12 | 4,08% |
| Boidin & Gilles (1986) | 11 | 2,14% | 11 | 3,7% | 8 | 2,72% | 10 | 3,4% |
| Boidin & Gilles (2000) | 10 | 1,95% | 10 | 3,37% | 10 | 3,4% | 10 | 3,4% |
| Jami et al. (2019) | 10 | 1,95% | 10 | 3,37% | 10 | 3,4% | 10 | 3,4% |
| Boidin & Gilles (1988) | 9 | 1,75% | 9 | 3,03% | 9 | 3,06% | 9 | 3,06% |
| Boidin & Gilles (1986) | 8 | 1,56% | 8 | 2,69% | 8 | 2,72% | 8 | 2,72% |
| Ordynets et al. (2018) | 8 | 1,56% | 8 | 2,69% | 8 | 2,72% | 8 | 2,72% |
| Boidin & Gilles (1986) | 7 | 1,36% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Boidin & Gilles (2001) | 7 | 1,36% | 7 | 2,36% | 7 | 2,38% | 7 | 2,38% |
| Boidin et al. (2004) | 7 | 1,36% | 7 | 2,36% | 7 | 2,38% | 7 | 2,38% |
| Boidin & Gilles (1986) | 6 | 1,17% | 5 | 1,68% | 5 | 1,7% | 5 | 1,7% |
| Boidin & Gilles (1994) | 6 | 1,17% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Boidin & Gilles (2000) | 6 | 1,17% | 6 | 2,02% | 6 | 2,04% | 6 | 2,04% |
| Boidin et al. (1987) | 6 | 1,17% | 6 | 2,02% | 6 | 2,04% | 6 | 2,04% |
| Elvebakk et al. (2016) | 6 | 1,17% | 6 | 2,02% | 6 | 2,04% | 6 | 2,04% |
| Ordynets et al. (2015) | 6 | 1,17% | 6 | 2,02% | 6 | 2,04% | 6 | 2,04% |
| Jaouen et al. (2019) | 5 | 0,97% | 5 | 1,68% | 5 | 1,7% | 4 | 1,36% |
| Jørgensen et al. (2009) | 5 | 0,97% | 5 | 1,68% | 5 | 1,7% | 5 | 1,7% |
| Ali et al. (2018) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| Boidin & Gilles (1986) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| Gruhn et al. (2017) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| Maas Geesteranus & Hausknecht (1996) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| Marin-Felix et al. (2019) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| The International Barcode of Life Consortium (2016) | 4 | 0,78% | 4 | 1,35% | 4 | 1,36% | 4 | 1,36% |
| Crous & Mourichon (2002) | 3 | 0,58% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Elia & Hentic (2003) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Ghobad-nejhad (2009) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Klaubauf et al. (2014) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Léger & Lanquetin (1889) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Maas Geesteranus & Hausknecht (1995) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Masson (2012) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Rivoire (2018) | 3 | 0,58% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Stadler et al. (2014) | 3 | 0,58% | 3 | 1,01% | 3 | 1,02% | 3 | 1,02% |
| Abraham (2021) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Antonín & Buyck (2006) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Aveskamp et al. (2010) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Balazuc (1975) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Balazuc (1975) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Boidin & Gilles (2000) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (2000) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Bourdot & Galzin (1928) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Braun et al. (2014) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Broeck et al. (2014) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Courtecuisse et al. (1996) | 2 | 0,39% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Crous et al. (2016) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Crous et al. (2019) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Duhem & Buyck (2012) | 2 | 0,39% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Duhem & Michel (2007) | 2 | 0,39% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Ertz et al. (2010) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ertz et al. (2017) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Frisch & Thor (2009) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Hafellner (1997) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kalb et al. (2009) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kalb et al. (2012) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kalb (2004) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kalb (2009) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kreisel & Hausknecht (2002) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Kreisel & Hausknecht (2006) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Krog (2000) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Léger & Lanquetin (1992) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Liu et al. (2019) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Maas Geesteranus & Hausknecht (1998) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Maas Geesteranus & Hausknecht (1998) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Marin-felix et al. (2019) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Miersch & Rödel (2010) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Miersch & Rödel (2011) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Nakasone (2013) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Riebesehl et al. (2015) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Riebesehl et al. (2019) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Robene-Soustrade et al. (2015) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Timdal & Krog (2001) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van den Boom et al. (2011) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Van den broeck et al. (2013) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Vánky (1996) | 2 | 0,39% | 2 | 0,67% | 2 | 0,68% | 2 | 0,68% |
| Vánky (2005) | 2 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2018) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Berrin et al. (2012) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Boidin (1957) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charron et al. (2018) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Duhem & Buyck (2011) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Elix (2009) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Ephytia (2020) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| European Nucleotide Archive (2019) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Hernández-Restrepo et al. (2022) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Horak & Mouchacca (1998) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Thomas et al. (2018) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Voiry et al. (2014) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
| Zhurbenko & Pino-Bodas (2017) | 1 | 0,19% | 1 | 0,34% | 1 | 0,34% | 1 | 0,34% |
