Fonge de Nouvelle-Calédonie
152 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Elix & McCarthy (1998) | 711 | 22,99% | 625 | 52,74% | 565 | 50,67% | 587 | 51,67% |
| Roux (2012) | 455 | 14,71% | 83 | 7% | 81 | 7,26% | 73 | 6,43% |
| Courtecuisse (2009) | 433 | 14% | 60 | 5,06% | 60 | 5,38% | 60 | 5,28% |
| Horak & Mouchacca (1998) | 285 | 9,21% | 169 | 14,26% | 165 | 14,8% | 169 | 14,88% |
| Boom et al. (2011) | 101 | 3,27% | 95 | 8,02% | 95 | 8,52% | 91 | 8,01% |
| Courtecuisse & Welti (2013) | 86 | 2,78% | 54 | 4,56% | 54 | 4,84% | 54 | 4,75% |
| Hekking & Sipman (1988) | 77 | 2,49% | 62 | 5,23% | 61 | 5,47% | 55 | 4,84% |
| Bricaud (2007) | 67 | 2,17% | 52 | 4,39% | 51 | 4,57% | 45 | 3,96% |
| Mouchacca & Horak (1998) | 66 | 2,13% | 61 | 5,15% | 59 | 5,29% | 61 | 5,37% |
| Braun et al. (1999) | 65 | 2,1% | 62 | 5,23% | 61 | 5,47% | 60 | 5,28% |
| Borgato et al. (2020) | 57 | 1,84% | 49 | 4,14% | 49 | 4,39% | 44 | 3,87% |
| Huguenin (1969) | 49 | 1,58% | 43 | 3,63% | 41 | 3,68% | 43 | 3,79% |
| Papong et al. (2014) | 47 | 1,52% | 45 | 3,8% | 45 | 4,04% | 45 | 3,96% |
| Louwhoff & Elix (2002) | 41 | 1,33% | 40 | 3,38% | 40 | 3,59% | 40 | 3,52% |
| Courtecuisse et al. (1996) | 37 | 1,2% | 27 | 2,28% | 27 | 2,42% | 27 | 2,38% |
| Roux & Coll (2020) | 36 | 1,16% | 12 | 1,01% | 12 | 1,08% | 12 | 1,06% |
| Aptroot & Lücking (2016) | 30 | 0,97% | 29 | 2,45% | 29 | 2,6% | 29 | 2,55% |
| Buyck (2013) | 26 | 0,84% | 21 | 1,77% | 21 | 1,88% | 21 | 1,85% |
| Aptroot et al. (2011) | 23 | 0,74% | 20 | 1,69% | 20 | 1,79% | 18 | 1,58% |
| Jaouen et al. (2019) | 21 | 0,68% | 15 | 1,27% | 15 | 1,35% | 15 | 1,32% |
| Imshaug (2019) | 19 | 0,61% | 15 | 1,27% | 15 | 1,35% | 14 | 1,23% |
| Courtecuisse (2006) | 17 | 0,55% | 16 | 1,35% | 16 | 1,43% | 16 | 1,41% |
| Abraham (2010) | 16 | 0,52% | 15 | 1,27% | 15 | 1,35% | 11 | 0,97% |
| Aptroot (2014) | 15 | 0,48% | 15 | 1,27% | 15 | 1,35% | 15 | 1,32% |
| Braun et al. (2014) | 15 | 0,48% | 15 | 1,27% | 15 | 1,35% | 15 | 1,32% |
| Lücking (2006) | 15 | 0,48% | 13 | 1,1% | 13 | 1,17% | 12 | 1,06% |
| Le Gallo (1952) | 14 | 0,45% | 9 | 0,76% | 9 | 0,81% | 5 | 0,44% |
| Bricaud (2009) | 12 | 0,39% | 12 | 1,01% | 12 | 1,08% | 11 | 0,97% |
| Crossay et al. (2018) | 12 | 0,39% | 9 | 0,76% | 9 | 0,81% | 9 | 0,79% |
| Eyssartier et al. (2011) | 12 | 0,39% | 12 | 1,01% | 12 | 1,08% | 12 | 1,06% |
| Huguenin (1969) | 12 | 0,39% | 12 | 1,01% | 12 | 1,08% | 12 | 1,06% |
| Abraham (2021) | 11 | 0,36% | 10 | 0,84% | 10 | 0,9% | 10 | 0,88% |
| Elix (2009) | 9 | 0,29% | 8 | 0,68% | 8 | 0,72% | 8 | 0,7% |
| Rivoire (2018) | 9 | 0,29% | 8 | 0,68% | 8 | 0,72% | 8 | 0,7% |
| Lücking & Kalb (2001) | 8 | 0,26% | 8 | 0,68% | 8 | 0,72% | 8 | 0,7% |
| Anonyme (2018) | 7 | 0,23% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Rogers & Ju (1998) | 7 | 0,23% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Elvebakk et al. (2016) | 6 | 0,19% | 6 | 0,51% | 6 | 0,54% | 6 | 0,53% |
| Kistenich et al. (2018) | 6 | 0,19% | 6 | 0,51% | 6 | 0,54% | 6 | 0,53% |
| Lebreton (2017) | 6 | 0,19% | 6 | 0,51% | 6 | 0,54% | 6 | 0,53% |
| Lécuru & Courtecuisse (2013) | 6 | 0,19% | 5 | 0,42% | 5 | 0,45% | 5 | 0,44% |
| Roux (2013) | 6 | 0,19% | 4 | 0,34% | 4 | 0,36% | 3 | 0,26% |
| Berndt (2013) | 5 | 0,16% | 5 | 0,42% | 5 | 0,45% | 5 | 0,44% |
| Buyck (2014) | 5 | 0,16% | 5 | 0,42% | 5 | 0,45% | 5 | 0,44% |
| Corriol & Roy (2021) | 5 | 0,16% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Jorgensen & Gjerde (2012) | 5 | 0,16% | 5 | 0,42% | 5 | 0,45% | 5 | 0,44% |
| Questel (2022) | 5 | 0,16% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Roux & Coll (2023) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eyssartier et al. (2008) | 4 | 0,13% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Pearson et al. (1922) | 4 | 0,13% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Roux & coll (2022) | 4 | 0,13% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Udagawa et al. (1994) | 4 | 0,13% | 4 | 0,34% | 4 | 0,36% | 4 | 0,35% |
| Buyck et al. (2012) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Ducousso et al. (2004) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Duhem & Buyck (2011) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Duhem & Buyck (2012) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Dupont et al. (2000) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Ephytia (2020) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Eyssartier et al. (2010) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Hughes et al. (2004) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Lebel et al. (2015) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Lebel et al. (2018) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Liberato & Barreto (2006) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lücking et al. (2016) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| McTaggart et al. (2008) | 3 | 0,1% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| O’Donnell et al. (2022) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Rikkinen et al. (2014) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Rikkinen et al. (2016) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Rivoire (2013) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Ryvarden (2005) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Videira et al. (2017) | 3 | 0,1% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Zaremski et al. (2014) | 3 | 0,1% | 3 | 0,25% | 3 | 0,27% | 3 | 0,26% |
| Archer & Elix (2009) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Armada (2018) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Berrin et al. (2012) | 2 | 0,06% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Bertrand & Roux (2018) | 2 | 0,06% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Bon (1999) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonati & Petitmengin (1907) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Buyck et al. (2017) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Buyck (2004) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Clauzade & Roux (1985) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corriol (2009) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Deighton (1974) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Döbbeler & Müller (2018) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Döbbeler (2005) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Elix (2019) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Elvebakk (2007) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Eyssartier & Ducousso (2017) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Hale (1976) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Hariot & Patouillard (1903) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heim (1966) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Hennings (1903) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Huguenin (1964) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Johnston et al. (2022) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Joshi et al. (2015) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Kalb & Elix (1998) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kalb et al. (2009) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Kalb (2008) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Kondratyuk et al. (2019) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Kwaśna & Nirenberg (2005) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Lebreton et al. (2023) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Lesdain (1910) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Looney et al. (2013) | 2 | 0,06% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Massee (1901) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Mckenzie & Kuthubutheen (1993) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Mckenzie (1995) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| O’donnell et al. (2004) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Schinz (1920) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Simon et al. (2018) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Smith (1965) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Spooner (1985) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Turcati (2019) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Udagawa et al. (1994) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Vouaux (1910) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Wakefield et al. (1916) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Wei et al. (2017) | 2 | 0,06% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
| Welti & Courtecuisse (2010) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aime & Mctaggart (2021) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Arup et al. (2013) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Błaszkowski et al. (2021) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Beller (1971) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boidin & Gilles (1989) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Buyck et al. (2016) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Buyck et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheype (2010) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Cooper (2011) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dai (2010) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Dennis (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flörke (1828) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritz-Sheridan & Portecop (1987) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Goffinet (1992) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Jørgensen et al. (2009) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Jørgensen (2014) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Leyronas et al. (2004) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Liberato et al. (2005) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Lücking et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Magain et al. (2012) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Massé (1982) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Müller (1893) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Noordeloos et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Padamsee & Mckenzie (2012) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Pée-laby (1896) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt et al. (2012) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Sérusiaux et al. (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1961) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Société et al. (1977) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stewart et al. (2018) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| inpn@mnhn.fr ">TINGUY Hugues |
1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Vondrák et al. (2019) | 1 | 0,03% | 1 | 0,08% | 1 | 0,09% | 1 | 0,09% |
| Wegensteiner et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhao et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
