Hépatiques
245 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Thouvenot et al. (2011) | 2127 | 48,7% | 794 | 45,82% | 733 | 46,42% | 744 | 45,7% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 1082 | 24,77% | 729 | 42,07% | 697 | 44,14% | 715 | 43,92% |
Bardat et al. (2021) | 689 | 15,77% | 197 | 11,37% | 178 | 11,27% | 177 | 10,87% |
Wigginton (2009) | 451 | 10,33% | 318 | 18,35% | 303 | 19,19% | 298 | 18,3% |
Hodgetts & Lockhart (2020) | 376 | 8,61% | 368 | 21,23% | 317 | 20,08% | 322 | 19,78% |
Ros et al. (2007) | 376 | 8,61% | 243 | 14,02% | 230 | 14,57% | 218 | 13,39% |
Grolle & Long (2000) | 295 | 6,75% | 195 | 11,25% | 195 | 12,35% | 175 | 10,75% |
Gradstein & Ilkiu-Borges (2009) | 240 | 5,49% | 187 | 10,79% | 180 | 11,4% | 180 | 11,06% |
Boggan et al. (1997) | 228 | 5,22% | 118 | 6,81% | 115 | 7,28% | 113 | 6,94% |
Véron et al. (2021) | 219 | 5,01% | 198 | 11,43% | 185 | 11,72% | 195 | 11,98% |
Grolle (1995) | 164 | 3,75% | 32 | 1,85% | 32 | 2,03% | 23 | 1,41% |
Gradstein & Hekking (1989) | 162 | 3,71% | 9 | 0,52% | 9 | 0,57% | 8 | 0,49% |
Grolle (2002) | 153 | 3,5% | 52 | 3% | 49 | 3,1% | 46 | 2,83% |
Hugonnot et al. (2017) | 94 | 2,15% | 62 | 3,58% | 62 | 3,93% | 46 | 2,83% |
Thouvenot (2023) | 76 | 1,74% | 37 | 2,14% | 37 | 2,34% | 36 | 2,21% |
Ah-Peng et al. (2010) | 50 | 1,14% | 39 | 2,25% | 36 | 2,28% | 39 | 2,4% |
Le Gallo (1951) | 50 | 1,14% | 30 | 1,73% | 30 | 1,9% | 21 | 1,29% |
Váňa et al. (2013) | 44 | 1,01% | 18 | 1,04% | 14 | 0,89% | 15 | 0,92% |
Lavocat Bernard (2018) | 40 | 0,92% | 36 | 2,08% | 34 | 2,15% | 35 | 2,15% |
Váňa et al. (2010) | 36 | 0,82% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Váňa et al. (2014) | 36 | 0,82% | 33 | 1,9% | 30 | 1,9% | 28 | 1,72% |
Reeb et al. (2022) | 33 | 0,76% | 16 | 0,92% | 16 | 1,01% | 16 | 0,98% |
Gradstein & Lavocat Bernard (2020) | 31 | 0,71% | 14 | 0,81% | 14 | 0,89% | 12 | 0,74% |
Söderström et al. (2013) | 31 | 0,71% | 12 | 0,69% | 10 | 0,63% | 11 | 0,68% |
Delamare et al. (1888) | 30 | 0,69% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Söderström et al. (2016) | 27 | 0,62% | 10 | 0,58% | 8 | 0,51% | 9 | 0,55% |
Dauphin (2003) | 26 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Cooper et al. (2013) | 25 | 0,57% | 9 | 0,52% | 9 | 0,57% | 9 | 0,55% |
Gradstein & Ilkiu-Borges (2015) | 25 | 0,57% | 14 | 0,81% | 12 | 0,76% | 14 | 0,86% |
Hodgetts et al. (2020) | 25 | 0,57% | 6 | 0,35% | 3 | 0,19% | 6 | 0,37% |
Ah-Peng et al. (2010) | 23 | 0,53% | 20 | 1,15% | 16 | 1,01% | 19 | 1,17% |
Sukkharak & Gradstein (2017) | 21 | 0,48% | 9 | 0,52% | 7 | 0,44% | 8 | 0,49% |
Gradstein & Reeb (2022) | 20 | 0,46% | 14 | 0,81% | 8 | 0,51% | 14 | 0,86% |
Sukkharak & Gradstein (2014) | 20 | 0,46% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Thouvenot et al. (2018) | 19 | 0,43% | 10 | 0,58% | 10 | 0,63% | 10 | 0,61% |
Váňa et al. (2012) | 19 | 0,43% | 8 | 0,46% | 6 | 0,38% | 5 | 0,31% |
Briscoe et al. (2015) | 18 | 0,41% | 8 | 0,46% | 8 | 0,51% | 8 | 0,49% |
Konstantinova & Vilnet (2009) | 17 | 0,39% | 5 | 0,29% | 5 | 0,32% | 3 | 0,18% |
Reeb & Bardat (2014) | 17 | 0,39% | 2 | 0,12% | 2 | 0,13% | 1 | 0,06% |
Reeb & Gradstein (2020) | 17 | 0,39% | 9 | 0,52% | 9 | 0,57% | 9 | 0,55% |
Stotler & Crandall-Stotler (2017) | 17 | 0,39% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Thouvenot & Müller (2021) | 15 | 0,34% | 15 | 0,87% | 15 | 0,95% | 15 | 0,92% |
Gradstein & Costa (2003) | 13 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldberg et al. (2010) | 11 | 0,25% | 5 | 0,29% | 5 | 0,32% | 5 | 0,31% |
Gradstein (2015) | 11 | 0,25% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lavocat Bernard & Reeb (2016) | 11 | 0,25% | 9 | 0,52% | 8 | 0,51% | 9 | 0,55% |
Pócs et al. (2015) | 11 | 0,25% | 5 | 0,29% | 5 | 0,32% | 5 | 0,31% |
Shaw et al. (2015) | 11 | 0,25% | 5 | 0,29% | 5 | 0,32% | 5 | 0,31% |
Patzak et al. (2016) | 10 | 0,23% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Grolle & Onraedt (1974) | 9 | 0,21% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Shi et al. (2015) | 9 | 0,21% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Söderström et al. (2010) | 9 | 0,21% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Stephani (1908) | 9 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Yu et al. (2014) | 9 | 0,21% | 8 | 0,46% | 3 | 0,19% | 5 | 0,31% |
Müller et al. (2016) | 8 | 0,18% | 8 | 0,46% | 8 | 0,51% | 8 | 0,49% |
Reiner-Drehwald & Grolle (2012) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Schütz et al. (2016) | 8 | 0,18% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Sukkharak (2015) | 8 | 0,18% | 4 | 0,23% | 2 | 0,13% | 3 | 0,18% |
Thiers (1993) | 8 | 0,18% | 6 | 0,35% | 6 | 0,38% | 6 | 0,37% |
Váňa et al. (2013) | 8 | 0,18% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Chatchaba et al. (2023) | 7 | 0,16% | 6 | 0,35% | 6 | 0,38% | 4 | 0,25% |
Chavoutier & Hugonnot (2013) | 7 | 0,16% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Ilkiu Borges (2006) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Passos Bastos & Gradstein (2020) | 7 | 0,16% | 3 | 0,17% | 0 | 0% | 3 | 0,18% |
Pócs & Bernecker (2009) | 7 | 0,16% | 5 | 0,29% | 5 | 0,32% | 4 | 0,25% |
Pócs (2011) | 7 | 0,16% | 2 | 0,12% | 2 | 0,13% | 1 | 0,06% |
Schuster (1969) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström et al. (2013) | 7 | 0,16% | 5 | 0,29% | 4 | 0,25% | 4 | 0,25% |
Váňa et al. (2010) | 7 | 0,16% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Váňa et al. (2013) | 7 | 0,16% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Váňa et al. (2013) | 7 | 0,16% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Bakalin (2011) | 6 | 0,14% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bescherelle (1898) | 6 | 0,14% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Gradstein (2013) | 6 | 0,14% | 4 | 0,23% | 4 | 0,25% | 3 | 0,18% |
Hodgetts (2008) | 6 | 0,14% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Konstantinova & Vasiljev (1994) | 6 | 0,14% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Söderström et al. (2015) | 6 | 0,14% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Gehrig-Downie et al. (2013) | 5 | 0,11% | 5 | 0,29% | 5 | 0,32% | 5 | 0,31% |
Rabeau et al. (2017) | 5 | 0,11% | 3 | 0,17% | 3 | 0,19% | 2 | 0,12% |
Renner et al. (2016) | 5 | 0,11% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Váňa et al. (2013) | 5 | 0,11% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Váňa et al. (2014) | 5 | 0,11% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Wei et al. (2014) | 5 | 0,11% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Ye et al. (2015) | 5 | 0,11% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Ah-Peng & Bardat (2005) | 4 | 0,09% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Cooper et al. (2011) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Dong et al. (2012) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Engel et al. (2012) | 4 | 0,09% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Engel et al. (2021) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Hentschel et al. (2007) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Hentschel et al. (2007) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Larraín et al. (2018) | 4 | 0,09% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Meyer & Ah-Peng (2024) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 2 | 0,12% |
Nadeaud (1873) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Renner (2016) | 4 | 0,09% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Schäfer-Verwimp (2014) | 4 | 0,09% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Segarra‐Moragues et al. (2022) | 4 | 0,09% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Shi et al. (2015) | 4 | 0,09% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Thouvenot (2015) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Tixier (1993) | 4 | 0,09% | 4 | 0,23% | 4 | 0,25% | 4 | 0,25% |
Bakalin et al. (2020) | 3 | 0,07% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Bakalin (2014) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Cooper et al. (2014) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Czumay et al. (2013) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein (2012) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Grolle (1972) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugonnot (2019) | 3 | 0,07% | 3 | 0,17% | 2 | 0,13% | 3 | 0,18% |
Konstantinova et al. (2021) | 3 | 0,07% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Long et al. (2016) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 0 | 0% |
Müller & Tan (2013) | 3 | 0,07% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Müller (2013) | 3 | 0,07% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Pócs & Váňa (2015) | 3 | 0,07% | 3 | 0,17% | 2 | 0,13% | 2 | 0,12% |
Pócs et al. (2014) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs et al. (2015) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs (2011) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Schill et al. (2008) | 3 | 0,07% | 3 | 0,17% | 1 | 0,06% | 2 | 0,12% |
Schill et al. (2010) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Schuette & Stotler 2005) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Shu et al. (2016) | 3 | 0,07% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot & Price (2020) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot (2021) | 3 | 0,07% | 3 | 0,17% | 3 | 0,19% | 3 | 0,18% |
Váňa et al. (2010) | 3 | 0,07% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Vana & Gremmen (2006) | 3 | 0,07% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ah-Peng & Bardat (2011) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Ah-Peng et al. (2008) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ångström (1873) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bechteler et al. (2017) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bonte et al. (2020) | 2 | 0,05% | 2 | 0,12% | 1 | 0,06% | 1 | 0,06% |
Crandall-Stotler & Stotler (2007) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Ellis et al. (2023) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Engel & Merrill (2004) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Frahm & Bick (2013) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Fuselier et al. (2011) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Gil-novoa et al. (2023) | 2 | 0,05% | 2 | 0,12% | 0 | 0% | 2 | 0,12% |
Gradstein & Ilkiu-borges (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
He et al. (2014) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Heinrichs et al. (2012) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Heinrichs et al. (2015) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Hugonnot (2010) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Katagiri (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lee & Pócs (2024) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Malombe (2009) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Marline (2018) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Martinez et al. (2014) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Montagne (1843) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Thouvenot (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Pearson (1922) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pócs (2006) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Qiu et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reiner-Drehwald & Schäfer-Verwimp (2008) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Renner et al. (2015) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Renner et al. (2024) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Rubasinghe et al. (2011) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Schäfer-Verwimp & Van Melick (2016) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Schiffner (1906) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Shu & Zhu (2019) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Shu et al. (2016) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Shu et al. (2016) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
So (2004) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Söderström et al. (2015) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Stephani (1924) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stotler (1969) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot & Bardat (2013) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Thouvenot & Engel (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot & Gradstein (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot & Reeb (2014) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot et al. (2015) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot (2002) | 2 | 0,05% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Thouvenot (2018) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Thouvenot (2018) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Thouvenot (2021) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Váňa & Gremmen (2005) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Váňa & Long (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2012) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Váňa et al. (2013) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Váňa et al. (2013) | 2 | 0,05% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Wickett & Goffinet (2008) | 2 | 0,05% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Zhu & Müller (2012) | 2 | 0,05% | 2 | 0,12% | 2 | 0,13% | 2 | 0,12% |
Ah-Peng & Bardat (2009) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ah-Peng (2007) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Anonyme. (2002) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Arts (2005) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bakalin et al. (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bakalin (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bastos & Gradstein (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bastos (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Blockeel et al. (2009) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bonte & Boudier (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Bonte & Boudier, 2022 | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Breton (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 0 | 0% |
Cailliau et al. (2013) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Chavoutier (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cordat (1829) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Coulis et al. (2022) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Dirkse & Losada-Lima (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dong et al. (2013) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ellis et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Ellis et al. (2023) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Engel & Braggins (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldberg et al. (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Frahm (2008) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Gradstein & Reeb (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gradstein (2015) | 1 | 0,02% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
He & Christenhusz (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hébrard (1970) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hébrard (1980) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Heinrichs et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heinrichs et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Holá (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hugonnot & Simont (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hugonnot et al. (2009) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Hugonnot et al. (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Lee et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meagher (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Müller (2007) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Onraedt & Cremers (1980) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Pocs (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Pócs (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Prey et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Reiner-Drehwald (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schafer-Verwimp & Reiner-Drehwald (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström et al. (2023) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Stephani (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephani (1908) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sun et al. (2018) | 1 | 0,02% | 1 | 0,06% | 0 | 0% | 1 | 0,06% |
Toussaint et al. (2013) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Uribe (2011) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
van Dort,& Smulders (2007) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Vanden Berghen (1984) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Vilnet et al. (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Vilnet et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Wang et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Yu et al. (2013) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Zamora et al. (1990) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |
Zhu et al. (2023) | 1 | 0,02% | 1 | 0,06% | 1 | 0,06% | 1 | 0,06% |