Hémiptères de Nouvelle-Calédonie
340 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fennah (1969) | 202 | 14,08% | 161 | 17,99% | 158 | 17,87% | 159 | 17,99% |
Mille et al. (2016) | 125 | 8,71% | 122 | 13,63% | 122 | 13,8% | 117 | 13,24% |
Matile-Ferrero & Etienne (2006) | 114 | 7,94% | 113 | 12,63% | 107 | 12,1% | 108 | 12,22% |
Jourdan & Mille (2006) | 103 | 7,18% | 95 | 10,61% | 95 | 10,75% | 88 | 9,95% |
Ramage (2017) | 98 | 6,83% | 94 | 10,5% | 92 | 10,41% | 90 | 10,18% |
Distant (1920) | 91 | 6,34% | 45 | 5,03% | 45 | 5,09% | 45 | 5,09% |
Montrouzier (1861) | 86 | 5,99% | 14 | 1,56% | 14 | 1,58% | 14 | 1,58% |
Meurgey & Ramage (2020) | 85 | 5,92% | 85 | 9,5% | 82 | 9,28% | 82 | 9,28% |
Meurgey (2011) | 83 | 5,78% | 81 | 9,05% | 79 | 8,94% | 77 | 8,71% |
Perroud & Montrouzier (1864) | 77 | 5,37% | 32 | 3,58% | 32 | 3,62% | 32 | 3,62% |
Distant (1914) | 73 | 5,09% | 35 | 3,91% | 35 | 3,96% | 35 | 3,96% |
Distant (1920) | 72 | 5,02% | 30 | 3,35% | 30 | 3,39% | 30 | 3,39% |
Hamilton (1981) | 62 | 4,32% | 51 | 5,7% | 51 | 5,77% | 51 | 5,77% |
Germain et al. (2014) | 49 | 3,41% | 48 | 5,36% | 48 | 5,43% | 46 | 5,2% |
Foldi & Germain (2018) | 44 | 3,07% | 43 | 4,8% | 42 | 4,75% | 38 | 4,3% |
Jourdan (2020) | 44 | 3,07% | 43 | 4,8% | 41 | 4,64% | 42 | 4,75% |
Schouteden (1907) | 44 | 3,07% | 27 | 3,02% | 27 | 3,05% | 27 | 3,05% |
Bourgoin (1997) | 43 | 3% | 40 | 4,47% | 40 | 4,52% | 40 | 4,52% |
Germain (2007) | 41 | 2,86% | 41 | 4,58% | 41 | 4,64% | 36 | 4,07% |
Guilbert (2002) | 40 | 2,79% | 39 | 4,36% | 39 | 4,41% | 39 | 4,41% |
Hill (2013) | 39 | 2,72% | 39 | 4,36% | 39 | 4,41% | 39 | 4,41% |
Montrouzier (1858) | 38 | 2,65% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Hosseini & Cassis (2019) | 37 | 2,58% | 37 | 4,13% | 37 | 4,19% | 37 | 4,19% |
Dumbleton (1961) | 36 | 2,51% | 32 | 3,58% | 32 | 3,62% | 32 | 3,62% |
Damgaard & Zettel (2014) | 35 | 2,44% | 34 | 3,8% | 33 | 3,73% | 33 | 3,73% |
Etienne (2005) | 35 | 2,44% | 35 | 3,91% | 35 | 3,96% | 35 | 3,96% |
Mille et al. (2020) | 33 | 2,3% | 32 | 3,58% | 32 | 3,62% | 32 | 3,62% |
Evans (1974) | 30 | 2,09% | 24 | 2,68% | 24 | 2,71% | 24 | 2,71% |
Mary (2017) | 30 | 2,09% | 28 | 3,13% | 27 | 3,05% | 27 | 3,05% |
Hardy & Williams (2018) | 28 | 1,95% | 28 | 3,13% | 28 | 3,17% | 28 | 3,17% |
Nielson (1975) | 25 | 1,74% | 25 | 2,79% | 25 | 2,83% | 25 | 2,83% |
Remillet (1988) | 25 | 1,74% | 20 | 2,23% | 19 | 2,15% | 17 | 1,92% |
Vayssières et al. (2001) | 25 | 1,74% | 23 | 2,57% | 23 | 2,6% | 21 | 2,38% |
Heiss (2011) | 23 | 1,6% | 23 | 2,57% | 23 | 2,6% | 23 | 2,6% |
Kormilev (1971) | 22 | 1,53% | 20 | 2,23% | 20 | 2,26% | 20 | 2,26% |
Boulard (1992) | 21 | 1,46% | 20 | 2,23% | 20 | 2,26% | 20 | 2,26% |
Cochereau (1966) | 21 | 1,46% | 21 | 2,35% | 21 | 2,38% | 20 | 2,26% |
Cohic (1959) | 21 | 1,46% | 16 | 1,79% | 16 | 1,81% | 14 | 1,58% |
Remaudière & Etienne (1988) | 21 | 1,46% | 21 | 2,35% | 21 | 2,38% | 21 | 2,38% |
Guilbert (2008) | 20 | 1,39% | 19 | 2,12% | 19 | 2,15% | 19 | 2,15% |
Etienne & Vilardebó (1978) | 18 | 1,25% | 17 | 1,9% | 17 | 1,92% | 14 | 1,58% |
Polhemus & Herring (1970) | 18 | 1,25% | 17 | 1,9% | 17 | 1,92% | 16 | 1,81% |
Cochereau (1974) | 16 | 1,11% | 16 | 1,79% | 15 | 1,7% | 15 | 1,7% |
Gutierrez (1981) | 16 | 1,11% | 13 | 1,45% | 13 | 1,47% | 13 | 1,47% |
Russell (1958) | 16 | 1,11% | 15 | 1,68% | 15 | 1,7% | 15 | 1,7% |
Anonyme (2018) | 15 | 1,05% | 15 | 1,68% | 14 | 1,58% | 15 | 1,7% |
Delorme (2017) | 15 | 1,05% | 15 | 1,68% | 15 | 1,7% | 15 | 1,7% |
Hamilton et al. (2017) | 15 | 1,05% | 15 | 1,68% | 15 | 1,7% | 15 | 1,7% |
Streito et al. (2007) | 15 | 1,05% | 15 | 1,68% | 15 | 1,7% | 15 | 1,7% |
Delorme (2017) | 14 | 0,98% | 14 | 1,56% | 14 | 1,58% | 14 | 1,58% |
Paulian (1998) | 14 | 0,98% | 13 | 1,45% | 13 | 1,47% | 13 | 1,47% |
Wygodzinsky (1966) | 14 | 0,98% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Boulard (1993) | 12 | 0,84% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Bhatti (1991) | 11 | 0,77% | 11 | 1,23% | 11 | 1,24% | 11 | 1,24% |
Zelazny & Webb (2011) | 11 | 0,77% | 11 | 1,23% | 11 | 1,24% | 11 | 1,24% |
Cheesman (1927) | 10 | 0,7% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Delorme et al. (2016) | 10 | 0,7% | 10 | 1,12% | 10 | 1,13% | 10 | 1,13% |
Hullé et al. (2018) | 10 | 0,7% | 10 | 1,12% | 10 | 1,13% | 10 | 1,13% |
Legros et al. (2017) | 10 | 0,7% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Lis (1997) | 10 | 0,7% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Matile-Ferrero (1979) | 10 | 0,7% | 10 | 1,12% | 10 | 1,13% | 9 | 1,02% |
Boulard (1991) | 9 | 0,63% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Boulard (1994) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Boulard (1997) | 9 | 0,63% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Cassis & Vanags (2006) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Cassis & Weirauch (2008) | 9 | 0,63% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Guilbert (1997) | 9 | 0,63% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Kormilev (1970) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Malipatil & Monteith (1983) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Questel (2020) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Sanborn (2018) | 9 | 0,63% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Dumbleton (1956) | 8 | 0,56% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert (1998) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Guilbert (2004) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Hollis & Broomfield (1989) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Linnaeus (1758) | 8 | 0,56% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Malipatil (1978) | 8 | 0,56% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Montrouzier (1855) | 8 | 0,56% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Murienne et al. (2009) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Nibouche et al. (202X) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 7 | 0,79% |
Questel & Le Quellec (2012) | 8 | 0,56% | 8 | 0,89% | 8 | 0,9% | 8 | 0,9% |
Burckhardt (2009) | 7 | 0,49% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Delorme (2018) | 7 | 0,49% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Guilbert (2014) | 7 | 0,49% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Kóbor (2023) | 7 | 0,49% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Lis (1999) | 7 | 0,49% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Matile-Ferrero & Williams (2015) | 7 | 0,49% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Cassis & Gross (2002) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Delorme et al. (2015) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Distant (1920) | 6 | 0,42% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Fennah (1958) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 5 | 0,57% |
Guilbert (1997) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Guilbert (1999) | 6 | 0,42% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Guilbert (2000) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Klyver (1932) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Knight (1983) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Matile-Ferrero & Balachowsky (1973) | 6 | 0,42% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Quilici et al. (1988) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 5 | 0,57% |
Scudder (1981) | 6 | 0,42% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Andersen & Weir (1999) | 5 | 0,35% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Bonfils et al. (1994) | 5 | 0,35% | 4 | 0,45% | 4 | 0,45% | 3 | 0,34% |
Cassis et al. (2003) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Cohic (1950) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Frenot et al. (2005) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Heiss (2011) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Hullé & Vernon (2021) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Matile-Ferrero et al. (2000) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Putshkov et al. (1999) | 5 | 0,35% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Slater (1964) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Van Duzee (1937) | 5 | 0,35% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Williams & Watson (1988) | 5 | 0,35% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Wolski & Gorczyca (2014) | 5 | 0,35% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Andersen & Weir (2000) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Bergroth (1914) | 4 | 0,28% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bigot (1992) | 4 | 0,28% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Boulard (1988) | 4 | 0,28% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
China (1957) | 4 | 0,28% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Delorme et al. (2016) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Gorczyca (1998) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Gorczyca (1999) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Heiss (2011) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Hill (2014) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Hoch et al. (2006) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Hodkinson (1983) | 4 | 0,28% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Hullé et al. (2003) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Hullé et al. (2010) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Kirkaldy (1905) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Kóbor (2020) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Lansbury (1970) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 3 | 0,34% |
Mound & Halsey (1978) | 4 | 0,28% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Russell & Etienne (1985) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Štys (1982) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Williams et al. (2006) | 4 | 0,28% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Ashlock (1967) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Boulard (1991) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Boulard (1993) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Cassis & Monteith (2006) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Cassis et al. (2019) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Cohic (1958) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Dadant & Etienne (1973) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Distant (1914) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Drake (1957) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Evans (1982) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Germain (2013) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Gorczyca (1997) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Gorczyca (1997) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Guilbert (2012) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Haupt (1927) | 3 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodgson et al. (2014) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Knight (2010) | 3 | 0,21% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kóbor & Kondorosy (2020) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Kreiter et al. (2022) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Lis & Lis (2010) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Lis (1999) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Lis (2009) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Löcker et al. (2006) | 3 | 0,21% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Löcker et al. (2006) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Lupoli (2023) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Martoni & Brown (2018) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Percy (2017) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Postle (2023) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Rageau (1958) | 3 | 0,21% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Román-Palacios et al. (2020) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Staddon (1997) | 3 | 0,21% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Stonedahl & Cassis (1991) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Stroiński (2010) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Štys (1981) | 3 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Adachi & Fullaway (1953) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkhsenius (1958) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Boulard & Moulds (2001) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bourgoin & Wilson (1992) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Carvalho (1973) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Carvalho (1977) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cassis & Silveira (2006) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cassis et al. (2017) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Chebbah et al. (2023) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cobben (1980) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cockerell (1893) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1959) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Donaldson (1988) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duay et al. (2014) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Esaki (1926) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Etienne & Matile-Ferrero (2008) | 2 | 0,14% | 2 | 0,22% | 0 | 0% | 2 | 0,23% |
Evans (1981) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ezzat (1958) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Fennah (1963) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1980) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ferris (1935) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gębicki et al. (2021) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Green (1930) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Hammes & Putoa (1986) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Hartung (2019) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Hiura (1966) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Horváth (1914) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Knight (1987) | 2 | 0,14% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kobor (2020) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kormilev (1968) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Kormilev (1971) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kozár (2004) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lallemand (1942) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lis (2006) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lundblad (1934) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lupoli & Dusoulier (2015) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Malipatil et al. (2022) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Malipatil (1983) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Martoni & Armstrong (2019) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Maskell (1893) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Matile-Ferrero (1988) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Mckamey (2010) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Mifsud et al. (2010) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Myers (1926) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Newstead (1908) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Osborn (1934) | 2 | 0,14% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Journal of the Australian Entomological Society, 26: 209-214. ">Polhemus & Polhemus (1987) |
2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Rageau (1959) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Scudder (1978) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sehnal (2000) | 2 | 0,14% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Streito et al. (2010) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Stys & Banar (2007) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Taquet et al. (2019) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Taszakowski et al. (2023) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Tatarnic et al. (2011) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Taylor et al. (2010) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Tsai & Redei (2014) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Van et al. (2010) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Vayssières et al. (2017) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Votýpka et al. (2020) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Wall & Cassis (2003) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Woodward (1958) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Woodward (1977) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Yang et al. (2023) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Zheng & Slater (1984) | 2 | 0,14% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Abraham (2022) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Albouy et al. (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Asche & Wilson (1990) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Balachowsky (1958) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Béguinot (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bencheton et al. (2011) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Berenger & Pluot-Sigwalt (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bigot (1985) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Biondi et al. (2013) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bondar (1923) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulard (1999) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bout et al. (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boyd et al. (2006) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boyer de Fonscolombe (1834) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Brinon et al. (2004) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brunhes (1979) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Callot (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Carvalho & Gross (1980) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cassis (2002) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chebbah et al. (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cochard et al. (2021) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cochereau (1966) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cochereau (1974) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cockerell (1895) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohic (1958) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coutiere & Martin (1901) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Delorme (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Disney & Chazeau (1990) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dispons (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Drake (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Drake (1942) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duan et al. (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ducos (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dupuis (1999) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duquef (2016) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duquef (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Elder & Abraham (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Elder (2016) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Elder (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Etienne et al. (1998) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Eyles & Malipatil (2010) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Eyles (1999) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fabres (1977) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fabricius (1775) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1794) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Forcellini et al. (2012) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Garrouste & Hervé (2009) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Garrouste (2015) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Germain & Streito (2004) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Germain et al. (2007) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Germain et al. (2014) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Goux (1937) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Green (1896) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Herring (1961) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hodgson et al. (2018) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Horvàth (1895) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jacobi (1922) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jansson (1982) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Kormilev (1965) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Lagarde (2008) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Latreille (1804) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Leavengood et al. (2024) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lethierry (1881) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lis (1994) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lowe et al. (2007) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lucas (1872) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Malausa & Ehanno (1988) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Malipatil (2010) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mamet (1959) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Martin (1985) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Matile-Ferrero & Etienne (1996) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Maurel (2016) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Metcalf (1955) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Morgan (1889) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Newstead (1909) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nieser & Chen (2005) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Normark et al. (2019) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poisson (1957) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Polhemus & Herring (1970) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Polhemus (2022) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Putshkov (1987) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Quaintance (1903) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ramage et al. (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sauvion et al. (1999) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Scudder (1958) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Seyfullah et al. (2017) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Streito et al. (2023) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Szita et al. (2020) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Takagi (1984) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thomas (1994) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tsai & Rédei (2010) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tuthill (1942) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Unruh & Gullan (2008) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandeschricke et al. (1992) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wang et al. (2014) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Watson et al. (2015) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams (1961) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang & Lu (2011) | 1 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |