Ptéridophytes de Guyane
Monilophyta et Lycopodiophyta de Guyane
135 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Funk et al. (2007) | 820 | 56,47% | 248 | 62,63% | 239 | 65,48% | 231 | 62,43% |
Cremers & Boudrie (2007) | 166 | 11,43% | 81 | 20,45% | 75 | 20,55% | 75 | 20,27% |
Christenhusz (2009) | 150 | 10,33% | 105 | 26,52% | 102 | 27,95% | 96 | 25,95% |
Bernard (2015) | 119 | 8,2% | 78 | 19,7% | 77 | 21,1% | 74 | 20% |
Øllgaard et al. (2020) | 75 | 5,17% | 11 | 2,78% | 8 | 2,19% | 9 | 2,43% |
Lehnert (2016) | 42 | 2,89% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Munzinger et al. (2016) | 38 | 2,62% | 11 | 2,78% | 11 | 3,01% | 9 | 2,43% |
Véron et al. (2021) | 30 | 2,07% | 30 | 7,58% | 29 | 7,95% | 29 | 7,84% |
Hovenkamp & Miyamoto (2005) | 26 | 1,79% | 5 | 1,26% | 5 | 1,37% | 4 | 1,08% |
Sant (2022) | 23 | 1,58% | 23 | 5,81% | 23 | 6,3% | 23 | 6,22% |
Mickel (2016) | 22 | 1,52% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Alston et al. (1981) | 21 | 1,45% | 21 | 5,3% | 21 | 5,75% | 21 | 5,68% |
Morat et al. (2012) | 21 | 1,45% | 11 | 2,78% | 11 | 3,01% | 8 | 2,16% |
Cárdenas et al. (2019) | 20 | 1,38% | 18 | 4,55% | 10 | 2,74% | 14 | 3,78% |
Prado & Moran (2008) | 20 | 1,38% | 9 | 2,27% | 9 | 2,47% | 9 | 2,43% |
Salino et al. (2015) | 20 | 1,38% | 11 | 2,78% | 8 | 2,19% | 8 | 2,16% |
Ebihara et al. (2006) | 18 | 1,24% | 6 | 1,52% | 6 | 1,64% | 6 | 1,62% |
Lehnert (2012) | 17 | 1,17% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Lehnert (2011) | 16 | 1,1% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Berry et al. (1995) | 15 | 1,03% | 6 | 1,52% | 6 | 1,64% | 6 | 1,62% |
Mynssen (2011) | 15 | 1,03% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Øllgaard & Windisch (2016) | 15 | 1,03% | 3 | 0,76% | 3 | 0,82% | 2 | 0,54% |
Sanín et al. (2023) | 15 | 1,03% | 6 | 1,52% | 6 | 1,64% | 6 | 1,62% |
Evrard et al. (2004) | 13 | 0,9% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Schwartsburd & Prado (2016) | 13 | 0,9% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Copeland (1932) | 12 | 0,83% | 8 | 2,02% | 8 | 2,19% | 4 | 1,08% |
Smith et al. (2006) | 12 | 0,83% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Almeida et al. (2016) | 11 | 0,76% | 11 | 2,78% | 11 | 3,01% | 10 | 2,7% |
Moran et al. (2010) | 11 | 0,76% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Murdock & Smith (2003) | 11 | 0,76% | 10 | 2,53% | 10 | 2,74% | 7 | 1,89% |
Rojas-alvarado (2017) | 11 | 0,76% | 6 | 1,52% | 6 | 1,64% | 6 | 1,62% |
Zuo et al. (2024) | 11 | 0,76% | 11 | 2,78% | 11 | 3,01% | 9 | 2,43% |
Bernard et al. (2014) | 10 | 0,69% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Christenhusz (2010) | 10 | 0,69% | 9 | 2,27% | 9 | 2,47% | 9 | 2,43% |
Clausen (1938) | 10 | 0,69% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Kessler et al. (2011) | 10 | 0,69% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Morat & Veillon (1985) | 10 | 0,69% | 9 | 2,27% | 9 | 2,47% | 5 | 1,35% |
Boudrie et al. (2017) | 9 | 0,62% | 7 | 1,77% | 7 | 1,92% | 7 | 1,89% |
Labiak et al. (2015) | 9 | 0,62% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Vasco et al. (2013) | 9 | 0,62% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Dubuisson et al. (2018) | 8 | 0,55% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Regalado Gabancho & Prada (2011) | 8 | 0,55% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Gasper et al. (2016) | 7 | 0,48% | 5 | 1,26% | 5 | 1,37% | 3 | 0,81% |
Lima et al. (2024) | 7 | 0,48% | 7 | 1,77% | 7 | 1,92% | 7 | 1,89% |
Tison et al. (2014) | 7 | 0,48% | 5 | 1,26% | 5 | 1,37% | 5 | 1,35% |
Holub (1985) | 6 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Boudrie (2006) | 5 | 0,34% | 3 | 0,76% | 2 | 0,55% | 3 | 0,81% |
Fourdrigniez & Meyer (2008) | 5 | 0,34% | 4 | 1,01% | 4 | 1,1% | 2 | 0,54% |
Lehnert & Weigand (2017) | 5 | 0,34% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Pteridophyte Phylogeny Group (2016) | 5 | 0,34% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Gonzales & Kessler (2011) | 4 | 0,28% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Hoff & Cremers (2005) | 4 | 0,28% | 3 | 0,76% | 1 | 0,27% | 3 | 0,81% |
Link-Pérez et al. (2016) | 4 | 0,28% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Meza-Torres (2015) | 4 | 0,28% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Prado & Windisch (2000) | 4 | 0,28% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Reed (1968) | 4 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Rojas-Alvarado & Tejero-Díez (2017) | 4 | 0,28% | 4 | 1,01% | 4 | 1,1% | 4 | 1,08% |
Schwartsburd & Prado (2015) | 4 | 0,28% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Wagner et al. (1984) | 4 | 0,28% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Zimmer (2007) | 4 | 0,28% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Boggan et al. (1992) | 3 | 0,21% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Boudrie & Cremers (2016) | 3 | 0,21% | 3 | 0,76% | 1 | 0,27% | 2 | 0,54% |
Boullet et al. (2018) | 3 | 0,21% | 2 | 0,51% | 2 | 0,55% | 1 | 0,27% |
Christenhusz (2006) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Christenhusz (2007) | 3 | 0,21% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Delnatte & Meyer (2012) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Field et al. (2016) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 2 | 0,54% |
Krömer et al. (2013) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Léotard & Chaline (2013) | 3 | 0,21% | 3 | 0,76% | 2 | 0,55% | 2 | 0,54% |
Matos & Mickel (2014) | 3 | 0,21% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Mickel (2008) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Mori et al. (1997) | 3 | 0,21% | 2 | 0,51% | 0 | 0% | 2 | 0,54% |
Morton & Lellinger (1971) | 3 | 0,21% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
øllgaard (2012) | 3 | 0,21% | 3 | 0,76% | 1 | 0,27% | 2 | 0,54% |
Prado & Lellinger (2002) | 3 | 0,21% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Rojas-alvarado (2008) | 3 | 0,21% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Shang & Zhang (2023) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Smith (1986) | 3 | 0,21% | 3 | 0,76% | 3 | 0,82% | 3 | 0,81% |
Boudrie & Bizot (2006) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Cremers & Boudrie (2007) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Ebihara et al. (2009) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 0 | 0% |
Heringer et al. (2016) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Korall et al. (2007) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Labiak et al. (2020) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Lamarck (1783) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Lehtonen et al. (2010) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Maddi (2010) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Mickel (1987) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Moran & Smith (1999) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Moran (2000) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 2 | 0,54% |
Questel (2023) | 2 | 0,14% | 2 | 0,51% | 2 | 0,55% | 1 | 0,27% |
Rudge (1805) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Schwartsburd et al. (2012) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Sundue & Prado (2005) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Tardieu-Blot (2008) | 2 | 0,14% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Viveros et al. (2018) | 2 | 0,14% | 2 | 0,51% | 1 | 0,27% | 1 | 0,27% |
Badré (2008b) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 0 | 0% |
Baker (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Barthelat (2019) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 0 | 0% |
Boggan et al. (1997) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudrie & Cremers (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boudrie & Cremers (2008) | 1 | 0,07% | 1 | 0,25% | 0 | 0% | 1 | 0,27% |
Cárdenas et al. (2016) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Cremers & Boudrie (2014) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Cremers & Hoff (1990) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Eppo (2011) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Forsskål (1775) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Geir (2018) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Grangaud (2010) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 0 | 0% |
Hequet & Le Corre (2010) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Hequet et al. (2009) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Kramer (1957) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Lazare et al. (1991) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Lellinger & Prado (2001) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
MacKee (1994) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Maddi (2014) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Maddi (2014) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Meyer et al. (2006) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Muller et al. (2004) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Navarrete & Øllgaard (2000) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Nitta et al. (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Paradis & Miniconi (2011) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Prado (2001) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Prado (2005) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Prelli & Boudrie (2021) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Ragavan et al. (2014) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Schuettpelz et al. (2016) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Sundue (2014) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Weigand & Lehnert (2016) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Wiersema et al. (2018) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2022) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Yahaya et al. (2016) | 1 | 0,07% | 1 | 0,25% | 0 | 0% | 1 | 0,27% |
Yesilyurt et al. (2015) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |
Zhang et al. (2013) | 1 | 0,07% | 1 | 0,25% | 1 | 0,27% | 1 | 0,27% |