Espèces signalées par erreur de la Réunion
430 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Grolle (1995) | 34 | 4% | 23 | 8,95% | 23 | 9,43% | 23 | 9,35% |
Lavocat Bernard & Schäfer-Verwimp (2011) | 33 | 3,88% | 21 | 8,17% | 19 | 7,79% | 20 | 8,13% |
Fournet (2002) | 32 | 3,76% | 32 | 12,45% | 32 | 13,11% | 32 | 13,01% |
Funk et al. (2007) | 24 | 2,82% | 8 | 3,11% | 8 | 3,28% | 7 | 2,85% |
Fricke et al. (2009) | 21 | 2,47% | 17 | 6,61% | 17 | 6,97% | 17 | 6,91% |
Fricke et al. (2011) | 18 | 2,12% | 16 | 6,23% | 16 | 6,56% | 16 | 6,5% |
Thouvenot et al. (2011) | 18 | 2,12% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Wigginton (2009) | 17 | 2% | 12 | 4,67% | 12 | 4,92% | 12 | 4,88% |
Bardat et al. (2021) | 15 | 1,76% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
O’Shea (2006) | 12 | 1,41% | 10 | 3,89% | 8 | 3,28% | 9 | 3,66% |
Du Puy et al. (1993) | 11 | 1,29% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Munzinger et al. (2016) | 11 | 1,29% | 4 | 1,56% | 4 | 1,64% | 3 | 1,22% |
Reeb et al. (2022) | 11 | 1,29% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Siu et al. (2017) | 10 | 1,18% | 9 | 3,5% | 9 | 3,69% | 9 | 3,66% |
Uicn et al. (2020) | 10 | 1,18% | 10 | 3,89% | 10 | 4,1% | 10 | 4,07% |
Martiré & Rochat (2008) | 9 | 1,06% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Pichon (2007) | 9 | 1,06% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Mattio et al. (2013) | 8 | 0,94% | 8 | 3,11% | 6 | 2,46% | 7 | 2,85% |
Pichon & Thomassin (2005) | 8 | 0,94% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Tison et al. (2014) | 8 | 0,94% | 7 | 2,72% | 7 | 2,87% | 7 | 2,85% |
Wilbraham & Ellis (2010) | 8 | 0,94% | 7 | 2,72% | 3 | 1,23% | 6 | 2,44% |
Williams et al. (2006) | 8 | 0,94% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Allen (comm. pers., 2009) | 7 | 0,82% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Aspock et al. (1980) | 7 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Benayahu & van Ofwegen (2012) | 7 | 0,82% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Goodman et al. (2010) | 7 | 0,82% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Hequet & Le Corre (2010) | 7 | 0,82% | 7 | 2,72% | 7 | 2,87% | 6 | 2,44% |
Hequet et al. (2009) | 7 | 0,82% | 7 | 2,72% | 7 | 2,87% | 6 | 2,44% |
Hermans & Cribb (2021) | 7 | 0,82% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
MacKee (1994) | 7 | 0,82% | 7 | 2,72% | 7 | 2,87% | 6 | 2,44% |
Morat et al. (2012) | 7 | 0,82% | 4 | 1,56% | 4 | 1,64% | 3 | 1,22% |
Bigot (comm. pers., 2018) | 6 | 0,71% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Ducarme (2023) | 6 | 0,71% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Gomy (2000) | 6 | 0,71% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Gradstein & Ilkiu-Borges (2009) | 6 | 0,71% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Keith et al. (2006) | 6 | 0,71% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Kulbicki et al. (2000) | 6 | 0,71% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Lambert (1988) | 6 | 0,71% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Morat & Veillon (1985) | 6 | 0,71% | 5 | 1,95% | 5 | 2,05% | 4 | 1,63% |
Pichon et al. (2007) | 6 | 0,71% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Ros et al. (2007) | 6 | 0,71% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Thouvenot & Bardat (2010) | 6 | 0,71% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Wickel & Jamon (2010) | 6 | 0,71% | 6 | 2,33% | 6 | 2,46% | 6 | 2,44% |
Boggan et al. (1997) | 5 | 0,59% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Clarke (1971) | 5 | 0,59% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Feliciano et al. (2021) | 5 | 0,59% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Mazancourt et al. (2019) | 5 | 0,59% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Øllgaard et al. (2020) | 5 | 0,59% | 2 | 0,78% | 1 | 0,41% | 1 | 0,41% |
Payri (2007) | 5 | 0,59% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Polanco & Acero (2016) | 5 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2022) | 5 | 0,59% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Uicn et al. (2017) | 5 | 0,59% | 5 | 1,95% | 5 | 2,05% | 5 | 2,03% |
Ah-Peng et al. (2010) | 4 | 0,47% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Bauters et al. (2019) | 4 | 0,47% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dupérré (2023) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Fourdrigniez & Meyer (2008) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 3 | 1,22% |
Gomy et al. (2016) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Gradstein & Hekking (1989) | 4 | 0,47% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Guillermet (2009) | 4 | 0,47% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Henderson & Breuil (2012) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Hodgetts & Lockhart (2020) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Hugonnot et al. (2017) | 4 | 0,47% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Kulbicki (comm. pers., 2011) | 4 | 0,47% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Levesque & Delcroix (2018) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Reese & Mohamed (1985) | 4 | 0,47% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Tirvengadum & Bour (1985) | 4 | 0,47% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Van Ofwegen (2007) | 4 | 0,47% | 4 | 1,56% | 4 | 1,64% | 4 | 1,63% |
Wilmot-Dear & Friis (2013) | 4 | 0,47% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bacchet et al. (2007) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Belfan & Conde (2016) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Borsa et al. (2014) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Bourmaud (2003) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Chabanet & Durville (2005) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Cheke (1987) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Christenhusz (2009) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 2 | 0,81% |
Collenette (1934) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Delnatte & Meyer (2012) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 2 | 0,81% |
Devantier et al. (2008) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2014) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (2004) | 3 | 0,35% | 1 | 0,39% | 0 | 0% | 1 | 0,41% |
Grolle & Long (2000) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Houart et al. (2015) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Jay et al. (2009) | 3 | 0,35% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ke et al. (2022) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Kükenthal (1936) | 3 | 0,35% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lagarde (2008) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Lamy & Pointier (2018) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Lavocat Bernard (2018) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Linnaeus (1753) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Linnaeus (1758) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Murdock & Smith (2003) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Poupin (2010) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Questel (2020) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Ramage (2017) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Safford & Hawkins (2013) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Shalisko et al. (2019) | 3 | 0,35% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Suessenguth (1936) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Tjeder (1940) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Viette (1949) | 3 | 0,35% | 3 | 1,17% | 3 | 1,23% | 3 | 1,22% |
Wasshausen (2006) | 3 | 0,35% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ah-Peng & Bardat (2005) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Allemand et al. (2002) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Alonso et al. (2018) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Alonso et al. (2019) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Améziane (2007) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Bauters et al. (2016) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Bippus (2020) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Briscoe et al. (2015) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Canard et al. (2014) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Cazanove (2022) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Charbonnel (1990) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Choy & Marquet (2002) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Clements (2012) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Colin (2000) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Conand & ARVAM (2005) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Copeland (1932) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Cuvier & Valenciennes (1836) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
David & Tsacas (1975) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
De Mazancourt et al. (2018) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Della & Giustina (2019) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Delrieu-Trottin et al. (2015) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Desjardins (1831) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorr & Wurdack (2020) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Fischer & Madl (2008) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Florschütz-de Waard et al. (2011) | 2 | 0,24% | 2 | 0,78% | 0 | 0% | 2 | 0,81% |
Gardner et al. (2021) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Guillermet (2006) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Guillermet (2011) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Hamon (1953) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Hamon (1956) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Haszprunar & Spies (2014) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Holloway (1979) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Hovenkamp & Miyamoto (2005) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
IUCN (2013) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Jiménez et al. (2017) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Keith et al. (1999) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Kessler et al. (2011) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Kronen et al. (2008) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Lacroix (1915) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Legand (1950) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Lemée (1955) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 1 | 0,41% |
Léong et al. (2003) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Linnaeus (1766) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsunuma et al. (2017) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Muru et al. (2017) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Nelson-Smith et al. (2014) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ohm & Hölzel (1997) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Parnaudeau (2009) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Parnaudeau (2017) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Pichon (comm. pers., 2012) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Questel & Le Quellec (2012) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Randall et al. (2015) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Remsen et al. (2013) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Richard et al. (1982) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2013) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Salazar-Vallejo (2020) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Schleyer & Benayahu (2016) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Schneider (1851) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrire et al. (2009) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Séméria & Quilici (1986) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Silva et al. (1996) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1997) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor & Elbel (1958) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Temminck et al. (1838) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Thierry & Canard (2019) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Tostain et al. (2013) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Tsacas & Chassagnard (1999) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Turak et al. (2008) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Turak et al. (2014) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Uicn et al. (2015) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Véron et al. (2021) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 1 | 0,41% |
Viane (2021) | 2 | 0,24% | 2 | 0,78% | 2 | 0,82% | 2 | 0,81% |
Yonow (2012) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2000) | 2 | 0,24% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Agarwal et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Albouy et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Allorge-Boiteau (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Almeida & Vasconcelos (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Almeida et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Alves et al. (2003) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Amati et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Angel (1939) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Anonyme. (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Anonyme (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnold (1980) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Aulagnier et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Aulagnier (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Aulagnier (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Austin & Arnold (2006) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Austin et al. (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Austin et al. (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Badonnel (1977) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bance (2022) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bangy et al. (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Barbour (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Béarez et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bento (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Berland (1934) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1942) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bidgrain (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (1862) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bippus (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bloch (1785-1795) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1794) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Boie (1827) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bollard et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bosser (1997) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bour (1981) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Bour (1984) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourdillon (1955) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Brake (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Breuil et al. (2010) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Breuil (2002) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Breuil (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Brun & Chazeau (1986) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Brunhes (1977) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Brunhes (1979) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Burel et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Busala et al. (2024) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Caceres (2002) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Caillot et al. (1999) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Callot & Rioux (1965) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Chapelin-Viscardi & Maillet-Mezeray (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chase et al. (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chocobar et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Chûjô (1964) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Conand & Ducarme (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Conand et al. (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Constantin (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Couté & Garrouste (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Cremers & Boudrie (2007) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Cuvier (1829) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Wynne (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Deuss et al. (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
deVantier et al. (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dewynter et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dewynter et al. (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dewynter et al. (2022) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dewynter et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dewynter et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dickinson & Remsen (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dierkens & Charlat (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Dierkens (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ditter et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dong et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Du Plessis et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Dulac (1867) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bribron (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebihara et al. (2006) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Elissa & Karch (2005) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Etcheberry et al. (1987) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Fabricius (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fairmaire (1899) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Faure et al. (2008) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Faure (1982) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Fauvel (1904) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fenner & Muir (2008) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ferragu (1979) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ferrer (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Field et al. (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Forskål (1775) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourriére et al. (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Fraga & Carvalho (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Franzini et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Frenot et al. (2001) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Fricke et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Galliard (1928) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Gargominy et al. (1996) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Gaudin (1828) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gauthier-clerc & Lambert (2002) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Girard (2007) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Glynn et al. (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran & Shine (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
González‐Elizondo & Peterson (1997) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
González-sánchez et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Gradstein & Reeb (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1821) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1825) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Guille et al. (1986) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Guillermet (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1876) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Harmon & Gibson (2006) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Henao-osorio et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Héros et al. (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hervé (2010) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgetts et al. (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Hoeksema et al. (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Hoeksema et al. (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Hustache (1920) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ifremer (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ineich et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Jairam et al. (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Jan & Sordelli (1860-1866) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Janák (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Jost et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Jourdan (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Jouventin (1994) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Kassebeer (1999) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Kassebeer (2000) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Kaszab (1982) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Keith et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Knoepffler et al. (1990) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Krömer et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Kuc (2006) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Lacroix (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1778) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lansdown (2022) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lavier (1936) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lavocat Bernard & Reeb (2016) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Bail et al. (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Léotard & Chaline (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ledoux & Hallé (1995) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Legros et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lemagnen (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Lescure (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Letty & Bouche (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Loveridge & Williams (1957) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Madl & van Achterberg (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Madl (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Mageski et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Marcos-garcía et al. (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Marinho (2022) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Marsh (1974) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Massary et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Massary et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Massary et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Matocq et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Mattio & Payri (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Mattio et al. (2015) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Meurgey & Ramage (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Meurgey (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Michenet & Bosserelle (2013) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Miller (1768) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mohamed et al. (2001) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Mohamed (1994) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Momont (1998) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau de Jonnès (1818) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mothes et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Munroe (1956) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1905) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1915) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navás (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Navas (1931) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollettino della Societa Entomologica Italiana, 65: 105-113.">Navas (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Nentwig et al. (2019) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Nibouche et al. (202X) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Nielsen & Quero (1991) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
N'Yeurt & Payri (2006) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Øllgaard & Windisch (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Ortea et al. (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ortea et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
O’shea et al. (2018) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Pailler & Henze (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Paperna & Landsberg (1989) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrier (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Pinaud et al. (2005) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Pleijel (2007) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Pont (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Poussereau (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Probst et al. (2000) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Probst (1998) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Probst (2001) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Questel et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Questel et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Questel (2016) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Quod et al. (1995) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Rabeau et al. (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Raibaut et al. (1979) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reeb & Bardat (2014) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Reverté et al. (2023) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ribaga (1904) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Risbec (1957) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1810) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Roalson et al. (2010) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Rojas-Alvarado (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Ronot (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1926) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Salisbury (1796) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Saunders (1883) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Schneider (1799) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Schur (1866) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sclater (1865) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Séret (1997) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Sheppard et al. (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
So (2004) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Solís-Marín & Laguarda Figueras (2009) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Sollman (2000) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1876) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1900) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephens (1835-1836) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sudre & Teocchi (1996) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Szlachetko et al. (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Thierry & Canard (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Tillier (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain & Dujardin (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Triest (1987) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Tröndlé & Boutet (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Tsacas (1980) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Vayssières et al. (2001) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Vences & Glaw (2003) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Verseveldt (1977) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Viette (1949) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Viette (1950) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Vogel et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Von May et al. (2021) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Vroman (1968) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Wantiez (2001) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Weimerskirch & Jouventin (1998) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Weterings & Vetter (2017) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Whatley & Keeler (1989) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Whittier (1976) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 0 | 0% |
Wickel et al. (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiebes (1981) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Wood et al. (2020) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |
Yarrell (1836) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2012) | 1 | 0,12% | 1 | 0,39% | 1 | 0,41% | 1 | 0,41% |