Ascidies
Ascidiacea
196 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Monniot (2007) | 289 | 14,37% | 239 | 30,92% | 238 | 30,87% | 237 | 30,74% |
Bay-nouailhat & Bay-nouailhat (2020) | 184 | 9,15% | 184 | 23,8% | 184 | 23,87% | 184 | 23,87% |
Monniot & Monniot (1983) | 100 | 4,97% | 87 | 11,25% | 87 | 11,28% | 87 | 11,28% |
Monniot & Monniot (1987) | 96 | 4,77% | 84 | 10,87% | 84 | 10,89% | 82 | 10,64% |
Ifremer (2009) | 78 | 3,88% | 73 | 9,44% | 73 | 9,47% | 73 | 9,47% |
Monniot & Monniot (1991) | 66 | 3,28% | 60 | 7,76% | 60 | 7,78% | 60 | 7,78% |
Giard (1872) | 58 | 2,88% | 6 | 0,78% | 6 | 0,78% | 6 | 0,78% |
Milne-Edwards (1841) | 58 | 2,88% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Kott (2001) | 49 | 2,44% | 44 | 5,69% | 44 | 5,71% | 44 | 5,71% |
Monniot (2016) | 45 | 2,24% | 40 | 5,17% | 40 | 5,19% | 40 | 5,19% |
Lafargue & Vasseur (1989) | 41 | 2,04% | 29 | 3,75% | 29 | 3,76% | 27 | 3,5% |
Monniot et al. (2011) | 38 | 1,89% | 38 | 4,92% | 38 | 4,93% | 38 | 4,93% |
Monniot (1978) | 38 | 1,89% | 33 | 4,27% | 33 | 4,28% | 33 | 4,28% |
Godet et al. (2010) | 32 | 1,59% | 29 | 3,75% | 29 | 3,76% | 29 | 3,76% |
Gravier (1955) | 31 | 1,54% | 17 | 2,2% | 17 | 2,2% | 16 | 2,08% |
Monniot & Gaill (1978) | 30 | 1,49% | 24 | 3,1% | 24 | 3,11% | 24 | 3,11% |
Monniot & Monniot (1974) | 29 | 1,44% | 22 | 2,85% | 22 | 2,85% | 22 | 2,85% |
Monniot (1988) | 29 | 1,44% | 22 | 2,85% | 22 | 2,85% | 22 | 2,85% |
Monniot (1983) | 28 | 1,39% | 16 | 2,07% | 16 | 2,08% | 16 | 2,08% |
Uicn et al. (2019) | 28 | 1,39% | 27 | 3,49% | 27 | 3,5% | 20 | 2,59% |
Monniot & Monniot (1985) | 27 | 1,34% | 18 | 2,33% | 18 | 2,33% | 18 | 2,33% |
Breton (2014) | 25 | 1,24% | 25 | 3,23% | 25 | 3,24% | 25 | 3,24% |
Monniot & Monniot (1974) | 24 | 1,19% | 19 | 2,46% | 19 | 2,46% | 19 | 2,46% |
Nelson-Smith et al. (2014) | 24 | 1,19% | 20 | 2,59% | 20 | 2,59% | 20 | 2,59% |
Monniot (1983) | 20 | 0,99% | 17 | 2,2% | 17 | 2,2% | 16 | 2,08% |
Arnaud (1974) | 19 | 0,94% | 17 | 2,2% | 17 | 2,2% | 17 | 2,2% |
Monniot (2018) | 19 | 0,94% | 18 | 2,33% | 18 | 2,33% | 18 | 2,33% |
Glémarec & Monniot (1966) | 18 | 0,9% | 18 | 2,33% | 18 | 2,33% | 18 | 2,33% |
Monniot (1983) | 18 | 0,9% | 17 | 2,2% | 17 | 2,2% | 16 | 2,08% |
Monniot (1983) | 17 | 0,85% | 13 | 1,68% | 13 | 1,69% | 13 | 1,69% |
Monniot & Dettai (2015) | 15 | 0,75% | 9 | 1,16% | 9 | 1,17% | 9 | 1,17% |
Bourcier (1988) | 14 | 0,7% | 13 | 1,68% | 13 | 1,69% | 13 | 1,69% |
Harant (1924) | 14 | 0,7% | 7 | 0,91% | 7 | 0,91% | 7 | 0,91% |
Monniot & Monniot (1984) | 13 | 0,65% | 9 | 1,16% | 9 | 1,17% | 9 | 1,17% |
Monniot & Monniot (2003) | 13 | 0,65% | 12 | 1,55% | 12 | 1,56% | 12 | 1,56% |
Monniot (1969) | 13 | 0,65% | 10 | 1,29% | 10 | 1,3% | 10 | 1,3% |
Monniot (1983) | 13 | 0,65% | 13 | 1,68% | 13 | 1,69% | 13 | 1,69% |
Monniot (1989) | 13 | 0,65% | 13 | 1,68% | 13 | 1,69% | 13 | 1,69% |
Goulletquer (2016) | 12 | 0,6% | 12 | 1,55% | 12 | 1,56% | 12 | 1,56% |
Monniot (1994) | 12 | 0,6% | 11 | 1,42% | 11 | 1,43% | 11 | 1,43% |
Monniot (2018) | 12 | 0,6% | 12 | 1,55% | 12 | 1,56% | 12 | 1,56% |
Monniot & Monniot (1977) | 11 | 0,55% | 11 | 1,42% | 11 | 1,43% | 11 | 1,43% |
Monniot & Monniot (1977) | 11 | 0,55% | 9 | 1,16% | 9 | 1,17% | 9 | 1,17% |
Monniot (1992) | 10 | 0,5% | 10 | 1,29% | 10 | 1,3% | 10 | 1,3% |
Pearman et al. (2020) | 10 | 0,5% | 9 | 1,16% | 8 | 1,04% | 9 | 1,17% |
Monniot (1969) | 9 | 0,45% | 9 | 1,16% | 9 | 1,17% | 9 | 1,17% |
Monniot (1984) | 9 | 0,45% | 8 | 1,03% | 6 | 0,78% | 8 | 1,04% |
Monniot & Monniot (2008) | 8 | 0,4% | 8 | 1,03% | 8 | 1,04% | 8 | 1,04% |
Monniot (2021) | 8 | 0,4% | 8 | 1,03% | 8 | 1,04% | 8 | 1,04% |
Monniot (1983) | 7 | 0,35% | 6 | 0,78% | 6 | 0,78% | 6 | 0,78% |
Monniot (2018) | 7 | 0,35% | 7 | 0,91% | 7 | 0,91% | 6 | 0,78% |
Questel (2020) | 7 | 0,35% | 6 | 0,78% | 6 | 0,78% | 6 | 0,78% |
Lafargue (1968) | 6 | 0,3% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1994) | 6 | 0,3% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Monniot (2007) | 6 | 0,3% | 6 | 0,78% | 6 | 0,78% | 6 | 0,78% |
Canu (1891) | 5 | 0,25% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Dewarumez et al. (2011) | 5 | 0,25% | 5 | 0,65% | 5 | 0,65% | 5 | 0,65% |
Monniot & Monniot (1973) | 5 | 0,25% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Monniot (2022) | 5 | 0,25% | 5 | 0,65% | 5 | 0,65% | 5 | 0,65% |
Müller (1776) | 5 | 0,25% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Sellier et al. (2016) | 5 | 0,25% | 5 | 0,65% | 5 | 0,65% | 5 | 0,65% |
Fourt et al. (2017) | 4 | 0,2% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Medioni (1970) | 4 | 0,2% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Millar (1977) | 4 | 0,2% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot (1990) | 4 | 0,2% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Schleyer et al. (2016) | 4 | 0,2% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Sentz‐Braconnot (1966) | 4 | 0,2% | 4 | 0,52% | 4 | 0,52% | 4 | 0,52% |
Shenkar & Swalla (2010) | 4 | 0,2% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Breton (2005) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Brunetti (1991) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Caullery (1914) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Chatton & Brément (1909) | 3 | 0,15% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gutt et al. (2007) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Harant (1930) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Kim & Boxshall (2020) | 3 | 0,15% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lafargue & Wahl (1987) | 3 | 0,15% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lahille (1890) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 3 | 0,15% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Debitus (2015) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot & Monniot (1987) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot & Monniot (2006) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot (comm. pers., 2012) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot (1970) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot (1978) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot (2011) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Monniot (2013) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Ordóñez et al. (2016) | 3 | 0,15% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Selys-Longchamps (1916) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Sluiter (1906) | 3 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Weinstein (1961) | 3 | 0,15% | 3 | 0,39% | 3 | 0,39% | 3 | 0,39% |
Alder (1863) | 2 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Australian Museum (2020) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bay-Nouailhat et al. (2020) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bocquet (1953) | 2 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bonnet & Lotufo (2015) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bouzon et al. (2014) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brément (1912) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Brement (1913) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Brunetti et al. (2015) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Caullery (1927) | 2 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Dauvin et al. (1991) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Davis & Davis (2009) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gail (1973) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Harant (1927) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Herdman (1882) | 2 | 0,1% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Koechlin (1977) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kott (1984) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lafargue (1975) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Martin (2011) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Maurice (1888) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Médioni (1968) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
MGnify (2017) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Millar & Goodbody (1974) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rep, 30: 1-160.">Millar (1960) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot & Monniot (1984) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1984) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1990) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
In: Crosnier, A. [Ed]. Résultats des Campagnes MUSORSTOM, Volume 21. Mémoires du Muséum national d'Histoire naturelle. Série A, Zoologie, 184: 703-721.">Monniot & Monniot (2000) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1970) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot (1986) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot (1994) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot (2002) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Monniot (2016) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pérez-Portela et al. (2007) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pineda et al. (2011) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pruvot-Fol (1929) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Questel & Le Quellec (2012) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rocha & Monniot (1993) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Sluiter (1890) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Sluiter (1904) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Traustedt (1882) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Turon et al. (2020) | 2 | 0,1% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Varnay (1955) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bishop et al. (2013) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bishop et al. (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brunetti & Mastrototaro (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brunetti (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Canu (1892) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chatton & Séguéla (1936) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Davis & Davis (2008) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Delle & Chiaje (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Eldredge (1967) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Fougue (1961) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Hartmeyer (1903) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Heller (1878) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Herdman (1883) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Herdman (1884) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Herdman (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hipeau-Jacquotte & Coste (1989) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kim & Boxshall (2021) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kott (1977) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kupffer (1875) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lamare (2012) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lambert (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lambert (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lizé (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lizé (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lizé (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
, 7: 181-260.">Michaelsen (1904) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Michaelsen (1921) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Monniot (1970) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Monniot (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot & Monniot (1985) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Monniot (1991) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Monniot (2001) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot & Tatián (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot et al. (1991) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1961) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1962) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1971) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1972) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monniot (1981) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1988) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (1997) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monniot (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Nydam & Harrison (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Oka (1927) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ooishi (2008) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pallas (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pizon (1896) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Renier (1804) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Richer de Forges et al. (2005) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Salfi (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Savigny (1816) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Stimpson (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tokioka (1954) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tokioka (1967) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Traustedt (1881) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ulman et al. (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Van Name (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Varela et al. (2007) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Zirpolo (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |