Fonge de la Réunion
146 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Roux (2012) | 444 | 26,15% | 93 | 12,38% | 93 | 12,45% | 93 | 12,45% |
| Boom et al. (2011) | 421 | 24,79% | 404 | 53,79% | 403 | 53,95% | 403 | 53,95% |
| Elix & McCarthy (1998) | 154 | 9,07% | 125 | 16,64% | 125 | 16,73% | 125 | 16,73% |
| Courtecuisse (2009) | 145 | 8,54% | 29 | 3,86% | 28 | 3,75% | 27 | 3,61% |
| Borgato et al. (2020) | 63 | 3,71% | 57 | 7,59% | 57 | 7,63% | 57 | 7,63% |
| Bricaud (2007) | 56 | 3,3% | 43 | 5,73% | 43 | 5,76% | 43 | 5,76% |
| Hekking & Sipman (1988) | 41 | 2,41% | 34 | 4,53% | 34 | 4,55% | 34 | 4,55% |
| Crous et al. (2016) | 36 | 2,12% | 30 | 3,99% | 30 | 4,02% | 30 | 4,02% |
| Brand et al. (2014) | 34 | 2% | 33 | 4,39% | 33 | 4,42% | 33 | 4,42% |
| Aptroot et al. (2011) | 33 | 1,94% | 25 | 3,33% | 25 | 3,35% | 25 | 3,35% |
| Boidin & Gilles (1991) | 30 | 1,77% | 22 | 2,93% | 22 | 2,95% | 22 | 2,95% |
| Boidin & Gilles (2000) | 27 | 1,59% | 27 | 3,6% | 27 | 3,61% | 27 | 3,61% |
| Fouillaud et al. (2017) | 24 | 1,41% | 19 | 2,53% | 19 | 2,54% | 19 | 2,54% |
| Roux & Coll (2020) | 24 | 1,41% | 9 | 1,2% | 9 | 1,2% | 9 | 1,2% |
| Imshaug (2019) | 21 | 1,24% | 16 | 2,13% | 16 | 2,14% | 16 | 2,14% |
| Mgnify (2018) | 20 | 1,18% | 16 | 2,13% | 16 | 2,14% | 16 | 2,14% |
| Noordeloos & Hausknecht (2007) | 20 | 1,18% | 20 | 2,66% | 20 | 2,68% | 20 | 2,68% |
| Lücking (2006) | 19 | 1,12% | 18 | 2,4% | 18 | 2,41% | 18 | 2,41% |
| Boidin & Gilles (1998) | 18 | 1,06% | 12 | 1,6% | 12 | 1,61% | 12 | 1,61% |
| Boidin et al. (1988) | 17 | 1% | 17 | 2,26% | 13 | 1,74% | 16 | 2,14% |
| Leger & Lanquetin (1986) | 17 | 1% | 17 | 2,26% | 17 | 2,28% | 17 | 2,28% |
| Courtecuisse & Welti (2013) | 16 | 0,94% | 15 | 2% | 15 | 2,01% | 12 | 1,61% |
| Boidin & Gilles (1989) | 15 | 0,88% | 14 | 1,86% | 14 | 1,87% | 14 | 1,87% |
| Crous et al. (2015) | 15 | 0,88% | 15 | 2% | 15 | 2,01% | 15 | 2,01% |
| Boidin & Gilles (1988) | 14 | 0,82% | 14 | 1,86% | 14 | 1,87% | 14 | 1,87% |
| Boidin et al. (1987) | 14 | 0,82% | 14 | 1,86% | 11 | 1,47% | 13 | 1,74% |
| Bricaud (2009) | 14 | 0,82% | 14 | 1,86% | 14 | 1,87% | 14 | 1,87% |
| Abraham (2010) | 13 | 0,77% | 13 | 1,73% | 13 | 1,74% | 13 | 1,74% |
| Buyck (2013) | 13 | 0,77% | 12 | 1,6% | 12 | 1,61% | 11 | 1,47% |
| Boidin & Gilles (1989) | 12 | 0,71% | 12 | 1,6% | 12 | 1,61% | 12 | 1,61% |
| Louwhoff & Elix (2002) | 12 | 0,71% | 11 | 1,46% | 11 | 1,47% | 11 | 1,47% |
| Boidin & Gilles (1986) | 11 | 0,65% | 11 | 1,46% | 8 | 1,07% | 10 | 1,34% |
| Le Gallo (1952) | 11 | 0,65% | 7 | 0,93% | 7 | 0,94% | 7 | 0,94% |
| Boidin & Gilles (2000) | 10 | 0,59% | 10 | 1,33% | 10 | 1,34% | 10 | 1,34% |
| Jami et al. (2019) | 10 | 0,59% | 10 | 1,33% | 10 | 1,34% | 10 | 1,34% |
| Boidin & Gilles (1988) | 9 | 0,53% | 9 | 1,2% | 9 | 1,2% | 9 | 1,2% |
| Boidin & Gilles (1986) | 8 | 0,47% | 8 | 1,07% | 8 | 1,07% | 8 | 1,07% |
| Masson et al. (2015) | 8 | 0,47% | 8 | 1,07% | 8 | 1,07% | 8 | 1,07% |
| Ordynets et al. (2018) | 8 | 0,47% | 8 | 1,07% | 8 | 1,07% | 8 | 1,07% |
| Boidin & Gilles (1986) | 7 | 0,41% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Boidin & Gilles (2001) | 7 | 0,41% | 7 | 0,93% | 7 | 0,94% | 7 | 0,94% |
| Boidin et al. (2004) | 7 | 0,41% | 7 | 0,93% | 7 | 0,94% | 7 | 0,94% |
| Roux & Coll (2023) | 7 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (1986) | 6 | 0,35% | 5 | 0,67% | 5 | 0,67% | 5 | 0,67% |
| Boidin & Gilles (1994) | 6 | 0,35% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Boidin & Gilles (2000) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Boidin et al. (1987) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Elvebakk et al. (2016) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Jørgensen et al. (2009) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Kalb & Aptroot (2021) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Ordynets et al. (2015) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Roux (2013) | 6 | 0,35% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Zhurbenko & Pino-Bodas (2017) | 6 | 0,35% | 6 | 0,8% | 6 | 0,8% | 6 | 0,8% |
| Jaouen et al. (2019) | 5 | 0,29% | 5 | 0,67% | 5 | 0,67% | 4 | 0,54% |
| Simon et al. (2018) | 5 | 0,29% | 5 | 0,67% | 5 | 0,67% | 5 | 0,67% |
| Ali et al. (2018) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Boidin & Gilles (1986) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Elix (2009) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Ertz et al. (2005) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Gruhn et al. (2017) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Maas Geesteranus & Hausknecht (1996) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Marin-Felix et al. (2019) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| The International Barcode of Life Consortium (2016) | 4 | 0,24% | 4 | 0,53% | 4 | 0,54% | 4 | 0,54% |
| Crous & Mourichon (2002) | 3 | 0,18% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Diederich et al. (2020) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Elia & Hentic (2003) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Ghobad-nejhad (2009) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Klaubauf et al. (2014) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Léger & Lanquetin (1889) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Maas Geesteranus & Hausknecht (1995) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Magain & Sérusiaux (2012) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Masson (2012) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Rivoire (2018) | 3 | 0,18% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Stadler et al. (2014) | 3 | 0,18% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
| Abraham (2021) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Antonín & Buyck (2006) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Aveskamp et al. (2010) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Balazuc (1975) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Balazuc (1975) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Boidin & Gilles (2000) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (2000) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Bourdot & Galzin (1928) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Braun et al. (2014) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Broeck et al. (2014) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Courtecuisse et al. (1996) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Crous et al. (2016) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Crous et al. (2019) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Duhem & Buyck (2012) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Duhem & Michel (2007) | 2 | 0,12% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Ertz et al. (2010) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ertz et al. (2017) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Frisch & Thor (2009) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Hafellner (1997) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kalb et al. (2009) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kalb et al. (2012) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kalb (2004) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kalb (2009) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kreisel & Hausknecht (2002) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Kreisel & Hausknecht (2006) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Krog (2000) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Lebreton (2017) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Léger & Lanquetin (1992) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Liu et al. (2019) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Maas Geesteranus & Hausknecht (1998) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Maas Geesteranus & Hausknecht (1998) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Marin-felix et al. (2019) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Masson et al. (2015) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Miersch & Rödel (2010) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Miersch & Rödel (2011) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Nakasone (2013) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Riebesehl et al. (2015) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Riebesehl et al. (2019) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Robene-Soustrade et al. (2015) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Suija et al. (2015) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Timdal & Krog (2001) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van den Boom et al. (2011) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Van den broeck et al. (2013) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Vánky (1996) | 2 | 0,12% | 2 | 0,27% | 2 | 0,27% | 2 | 0,27% |
| Vánky (2005) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Aptroot & Lücking (2016) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Berrin et al. (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Boidin (1957) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charron et al. (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Coste & Pinault (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Duhem & Buyck (2011) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Ephytia (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| European Nucleotide Archive (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Fritz-Sheridan & Portecop (1987) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Harris (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Hernández-Restrepo et al. (2022) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Hongsanan et al. (2020) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Horak & Mouchacca (1998) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Joshi et al. (2015) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Kalb & Elix (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lücking et al. (2013) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magain et al. (2012) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Massé (1982) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Masson & Bauvet (2021) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Øvstedal & Gremmen (2009) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Roux & Coll. (2017) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Roux & coll (2022) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Thomas et al. (2018) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Thomson (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turcati (2019) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
| Voiry et al. (2014) | 1 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
