Diptères Syrphidae de France métropolitaine
212 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Reverté et al. (2023) | 583 | 46,75% | 576 | 96,81% | 576 | 96,97% | 575 | 96,8% |
| Speight (2013) | 558 | 44,75% | 514 | 86,39% | 514 | 86,53% | 513 | 86,36% |
| Lebard & Speight (2019) | 282 | 22,61% | 269 | 45,21% | 269 | 45,29% | 268 | 45,12% |
| Meigen (1822) | 98 | 7,86% | 34 | 5,71% | 34 | 5,72% | 34 | 5,72% |
| Speight & Sarthou (2006) | 45 | 3,61% | 42 | 7,06% | 42 | 7,07% | 42 | 7,07% |
| Linnaeus (1758) | 34 | 2,73% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fallén (1817) | 27 | 2,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1794) | 22 | 1,76% | 0 | 0% | 0 | 0% | 0 | 0% |
| Becker (1894) | 20 | 1,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speight & Castella (2011) | 19 | 1,52% | 18 | 3,03% | 18 | 3,03% | 18 | 3,03% |
| Fabricius (1805) | 12 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goeldlin de Tiefnau (1974) | 11 | 0,88% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Treiber (2011) | 11 | 0,88% | 9 | 1,51% | 9 | 1,52% | 9 | 1,52% |
| Speight (2015) | 9 | 0,72% | 7 | 1,18% | 7 | 1,18% | 7 | 1,18% |
| Speight (2018) | 9 | 0,72% | 5 | 0,84% | 5 | 0,84% | 5 | 0,84% |
| Harris (1776-[1780]) | 8 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lebard et al. (2019) | 7 | 0,56% | 7 | 1,18% | 7 | 1,18% | 7 | 1,18% |
| Maibach et al. (1994) | 7 | 0,56% | 7 | 1,18% | 7 | 1,18% | 7 | 1,18% |
| Redon & Chorein (2009) | 7 | 0,56% | 6 | 1,01% | 6 | 1,01% | 6 | 1,01% |
| Speight et al. (2021) | 7 | 0,56% | 7 | 1,18% | 7 | 1,18% | 7 | 1,18% |
| Speight (2011) | 7 | 0,56% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Becker (1921) | 6 | 0,48% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Doczkal (1996) | 6 | 0,48% | 6 | 1,01% | 6 | 1,01% | 6 | 1,01% |
| Fabricius (1775) | 6 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goeldlin (1971) | 6 | 0,48% | 6 | 1,01% | 6 | 1,01% | 6 | 1,01% |
| Strobl (1909) | 6 | 0,48% | 6 | 1,01% | 6 | 1,01% | 6 | 1,01% |
| Vujić et al. (2013) | 6 | 0,48% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Zetterstedt (1838) | 6 | 0,48% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Albouy et al. (2017) | 5 | 0,4% | 5 | 0,84% | 5 | 0,84% | 5 | 0,84% |
| Dusek & Laska (1973) | 5 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lair (2018) | 5 | 0,4% | 5 | 0,84% | 5 | 0,84% | 5 | 0,84% |
| Nedeljković et al. (2018) | 5 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nielsen (2004) | 5 | 0,4% | 5 | 0,84% | 5 | 0,84% | 5 | 0,84% |
| Panzer (1798-1810) | 5 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Speight & Sarthou (2008) | 5 | 0,4% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Tissot et al. (2013) | 5 | 0,4% | 5 | 0,84% | 5 | 0,84% | 5 | 0,84% |
| Goeldlin & Tiefenau (1989) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Goeldlin et al. (1982) | 4 | 0,32% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Kassebeer (2000) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Lair et al. (2022) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Macquart (1829) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maillet-Mezeray et al. (2012) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Marcos-Garcia et al. (2007) | 4 | 0,32% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Marcos-garcía et al. (2013) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Matile & Leclercq (1992) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Panzer (1792-1798) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perris (1839) | 4 | 0,32% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Rossi (1790) | 4 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Séguy (1961) | 4 | 0,32% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Smit & Vujić (2008) | 4 | 0,32% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Speight & Ricarte (2012) | 4 | 0,32% | 4 | 0,67% | 4 | 0,67% | 4 | 0,67% |
| Speight et al. (2018) | 4 | 0,32% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Vujić et al. (2021) | 4 | 0,32% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Bot et al. (2023) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Cavaillès (2020) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Classen (1998) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Claussen & Kassebeer (1993) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Claussen (1991) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dusek & Laska (1982) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Fabricius ([1777]) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haarto & Ståhls (2014) | 3 | 0,24% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Kassebeer (1991) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Neve (2015) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Sack (1913) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Schmid (2000) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Speight & Claussen (1987) | 3 | 0,24% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Speight & Langlois (2020) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Speight & Lebard (2022) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Timon-david (1937) | 3 | 0,24% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Verlinden (1999) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Vockeroth (1990) | 3 | 0,24% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Vujić et al. (2012) | 3 | 0,24% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Vujic & Claussen (1994) | 3 | 0,24% | 3 | 0,5% | 3 | 0,51% | 3 | 0,51% |
| Aguado-Aranda et al. (2024) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Barkalov & Stahls (1997) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Bigot (1862) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Collin (1940) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Collin (1952) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| d'Aguilar & Coutin (1988) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 0 | 0% |
| Doczkal et al. (1994) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Doczkal et al. (2002) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Doczkal (2000) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Dufour (1848) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Egger (1858) | 2 | 0,16% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Egger (1865) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1781) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourcroy (1785) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goeldlin & Tiefenau (1997) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Goeldlin et al. (1990) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Hippa (1968) | 2 | 0,16% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lair & Livory (2016) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Likov et al. (2019) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loew (1856) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Lyneborg & Barkemeyer (2005) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Macquart (1842) | 2 | 0,16% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Marcos et al. (1983) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marcos-garcia et al. (2000) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Marcos-Garcia et al. (2011) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Mengual (2018) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Popović et al. (2015) | 2 | 0,16% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Reemer (2000) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Ricarte et al. (2022) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Rome (2016) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Rondani (1844) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Rossi (1794) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rotheray (1998) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Schiner & Egger (1853) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Scopoli (1763) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simic (1987) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Skevington & Thompson (2012) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Speight et al. (2016) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| , 32: 197-209.">Stanescu (1992) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Szilady (1937) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Tissot et al. (2019) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Van de Meutter (2022) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Vayssières et al. (2001) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Villers (1789) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Violovich (1956) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vujić et al. (2024) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Vujic & Claussen (2000) | 2 | 0,16% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Šašić et al. (2016) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Andréu (1926) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bagachanova (1980) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Becher (1882) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot (1884) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Claude et al. (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Claussen (1989) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Cornuel-Willermoz et al. (2023) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Cornuel-willermoz (2021) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Czerny & Strobl (1909) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Descaves & Speight (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Desmarest (1843) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Dusek & Laska (1976) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dussaix et al. (2007) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Egger (1859) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Etcheberry & Abraham (2009) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Fabricius (1787) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forster (1771) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1790) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulson & Wright (1998) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Grković et al. (2015) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Houard & Speight (2010) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| ICZN (2001) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Kassebeer (1995) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kassebeer (1999) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Kowarz (1885) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Langlois & Speight (2020) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Latreille (1809) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lauriaut & Lair (2018) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Linnaeus (1761) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Livory & Coulomb (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Loew (1843) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loew (1843) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Loew (1871) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louboutin & Speight (2021) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Macquart (1834) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Marcuzzi (1941) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Matsumura (1911) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1804) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1830) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meigen (1838) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Mengual & Ssymank (2015) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Mengual et al. (2015) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Mik (1885) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Mutin (1990) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Nedeljković et al. (2015) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Osten-sacken (1877) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Pérez et al. (2003) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poulin (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Ricarte et al. (2017) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robineau-desvoidy (1844) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Rondani (1845) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roser (1840) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sagot et al. (2004) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Savina (2016) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Schiner & Egger (1853) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmid (1999) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simic & Vujic (1996) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Sommaggio (2001) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Soszyński et al. (2013) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight & Garrigue (2016) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight & Labatut (2022) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight & Lebart (2022) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight & Vanappelghem (2018) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight et al. (2005) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight et al. (2013) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight et al. (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight (2007) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Speight (2018) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Ståhls & Barkalov (2017) | 1 | 0,08% | 1 | 0,17% | 0 | 0% | 1 | 0,17% |
| Ståhls et al. (2004) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Stănescu (1981) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Strobl (1893) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Strobl (1898) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Strobl (1910) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stubbs (2002) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Tissot et al. (2019) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Tissot et al. (2021) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Ueda (2020) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Vallet (2010) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Van et al. (1969) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| van Steenis et al. (2020) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| van Steenis (2000) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Veselić et al. (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Vidal (2023) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Violovich (1975) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiedemann (1830) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Withers (2007) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Withers (2017) | 1 | 0,08% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Zilli (2021) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
