Hémiptères de Polynésie française
236 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ramage (2017) | 415 | 54,32% | 404 | 91,2% | 392 | 91,8% | 402 | 93,27% |
Fennah (1958) | 139 | 18,19% | 139 | 31,38% | 137 | 32,08% | 138 | 32,02% |
Matile-Ferrero & Etienne (2006) | 86 | 11,26% | 85 | 19,19% | 81 | 18,97% | 76 | 17,63% |
China (1933) | 70 | 9,16% | 10 | 2,26% | 7 | 1,64% | 10 | 2,32% |
Meurgey & Ramage (2020) | 70 | 9,16% | 70 | 15,8% | 68 | 15,93% | 67 | 15,55% |
Meurgey (2011) | 68 | 8,9% | 64 | 14,45% | 63 | 14,75% | 60 | 13,92% |
Jourdan & Mille (2006) | 56 | 7,33% | 52 | 11,74% | 52 | 12,18% | 47 | 10,9% |
Mille et al. (2016) | 56 | 7,33% | 54 | 12,19% | 54 | 12,65% | 49 | 11,37% |
Mckamey (2010) | 37 | 4,84% | 25 | 5,64% | 24 | 5,62% | 24 | 5,57% |
Cheesman (1927) | 36 | 4,71% | 34 | 7,67% | 34 | 7,96% | 34 | 7,89% |
Foldi & Germain (2018) | 36 | 4,71% | 35 | 7,9% | 33 | 7,73% | 31 | 7,19% |
Germain et al. (2014) | 35 | 4,58% | 34 | 7,67% | 34 | 7,96% | 33 | 7,66% |
Van Duzee (1932) | 35 | 4,58% | 28 | 6,32% | 28 | 6,56% | 28 | 6,5% |
Germain (2007) | 33 | 4,32% | 33 | 7,45% | 33 | 7,73% | 29 | 6,73% |
Etienne (2005) | 30 | 3,93% | 27 | 6,09% | 27 | 6,32% | 27 | 6,26% |
Osborn (1934) | 30 | 3,93% | 27 | 6,09% | 25 | 5,85% | 27 | 6,26% |
Hamilton (1980) | 29 | 3,8% | 29 | 6,55% | 27 | 6,32% | 29 | 6,73% |
Paulian (1998) | 28 | 3,66% | 26 | 5,87% | 26 | 6,09% | 26 | 6,03% |
Wygodzinsky (1966) | 24 | 3,14% | 13 | 2,93% | 13 | 3,04% | 13 | 3,02% |
Cochereau (1966) | 23 | 3,01% | 23 | 5,19% | 23 | 5,39% | 22 | 5,1% |
Hoch (2006) | 23 | 3,01% | 23 | 5,19% | 23 | 5,39% | 23 | 5,34% |
Cochereau (1974) | 22 | 2,88% | 22 | 4,97% | 21 | 4,92% | 22 | 5,1% |
Polhemus (2022) | 22 | 2,88% | 22 | 4,97% | 22 | 5,15% | 22 | 5,1% |
Remillet (1988) | 21 | 2,75% | 18 | 4,06% | 18 | 4,22% | 15 | 3,48% |
Cohic (1959) | 19 | 2,49% | 13 | 2,93% | 13 | 3,04% | 11 | 2,55% |
Jourdan (2020) | 19 | 2,49% | 19 | 4,29% | 18 | 4,22% | 18 | 4,18% |
Van Duzee (1934) | 19 | 2,49% | 18 | 4,06% | 18 | 4,22% | 18 | 4,18% |
Vayssières et al. (2001) | 19 | 2,49% | 16 | 3,61% | 16 | 3,75% | 16 | 3,71% |
Anonyme (2018) | 16 | 2,09% | 16 | 3,61% | 15 | 3,51% | 16 | 3,71% |
Etienne & Vilardebó (1978) | 16 | 2,09% | 15 | 3,39% | 15 | 3,51% | 13 | 3,02% |
Polhemus (2010) | 16 | 2,09% | 16 | 3,61% | 16 | 3,75% | 16 | 3,71% |
Streito et al. (2007) | 16 | 2,09% | 16 | 3,61% | 16 | 3,75% | 16 | 3,71% |
Schuh (1984) | 14 | 1,83% | 14 | 3,16% | 14 | 3,28% | 14 | 3,25% |
Gutierrez (1981) | 13 | 1,7% | 10 | 2,26% | 10 | 2,34% | 10 | 2,32% |
Hodkinson (1983) | 13 | 1,7% | 12 | 2,71% | 12 | 2,81% | 12 | 2,78% |
Klyver (1932) | 13 | 1,7% | 8 | 1,81% | 8 | 1,87% | 8 | 1,86% |
Kobor (2020) | 13 | 1,7% | 13 | 2,93% | 13 | 3,04% | 13 | 3,02% |
Mille et al. (2020) | 12 | 1,57% | 11 | 2,48% | 11 | 2,58% | 11 | 2,55% |
Namyatova & Cassis (2016) | 12 | 1,57% | 12 | 2,71% | 12 | 2,81% | 12 | 2,78% |
Remaudière & Etienne (1988) | 12 | 1,57% | 10 | 2,26% | 10 | 2,34% | 10 | 2,32% |
Van Duzee (1937) | 12 | 1,57% | 11 | 2,48% | 10 | 2,34% | 11 | 2,55% |
Legros et al. (2017) | 11 | 1,44% | 9 | 2,03% | 9 | 2,11% | 9 | 2,09% |
Klyver (1932) | 10 | 1,31% | 9 | 2,03% | 9 | 2,11% | 9 | 2,09% |
Lallemand (1937) | 10 | 1,31% | 10 | 2,26% | 7 | 1,64% | 10 | 2,32% |
Lundblad (1934) | 10 | 1,31% | 10 | 2,26% | 10 | 2,34% | 10 | 2,32% |
Matile-Ferrero (1979) | 9 | 1,18% | 9 | 2,03% | 9 | 2,11% | 9 | 2,09% |
Montrouzier (1861) | 9 | 1,18% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Osborn (1934) | 9 | 1,18% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Martoni & Brown (2018) | 8 | 1,05% | 8 | 1,81% | 8 | 1,87% | 8 | 1,86% |
Questel (2020) | 8 | 1,05% | 8 | 1,81% | 8 | 1,87% | 7 | 1,62% |
Bonfils et al. (1994) | 7 | 0,92% | 6 | 1,35% | 6 | 1,41% | 6 | 1,39% |
Distant (1920) | 7 | 0,92% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Fennah (1969) | 7 | 0,92% | 5 | 1,13% | 5 | 1,17% | 5 | 1,16% |
Hammes & Putoa (1986) | 7 | 0,92% | 7 | 1,58% | 6 | 1,41% | 7 | 1,62% |
Kormilev (1971) | 7 | 0,92% | 5 | 1,13% | 5 | 1,17% | 5 | 1,16% |
Montrouzier (1858) | 7 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Percy (2017) | 7 | 0,92% | 7 | 1,58% | 7 | 1,64% | 7 | 1,62% |
Perroud & Montrouzier (1864) | 7 | 0,92% | 0 | 0% | 0 | 0% | 0 | 0% |
Schouteden (1907) | 7 | 0,92% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Knight (1937) | 6 | 0,79% | 6 | 1,35% | 6 | 1,41% | 6 | 1,39% |
Matile-Ferrero & Williams (2015) | 6 | 0,79% | 6 | 1,35% | 6 | 1,41% | 6 | 1,39% |
Nibouche et al. (202X) | 6 | 0,79% | 6 | 1,35% | 6 | 1,41% | 5 | 1,16% |
Tuthill (1942) | 6 | 0,79% | 6 | 1,35% | 6 | 1,41% | 6 | 1,39% |
Distant (1914) | 5 | 0,65% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Knight (2010) | 5 | 0,65% | 5 | 1,13% | 5 | 1,17% | 5 | 1,16% |
Linnaeus (1758) | 5 | 0,65% | 2 | 0,45% | 2 | 0,47% | 1 | 0,23% |
Questel & Le Quellec (2012) | 5 | 0,65% | 5 | 1,13% | 5 | 1,17% | 4 | 0,93% |
Román-Palacios et al. (2020) | 5 | 0,65% | 5 | 1,13% | 5 | 1,17% | 5 | 1,16% |
Russell & Etienne (1985) | 5 | 0,65% | 5 | 1,13% | 5 | 1,17% | 5 | 1,16% |
Damgaard & Zettel (2014) | 4 | 0,52% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Ferris (1935) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Garrouste & Hervé (2009) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Knight (1938) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Knight (1987) | 4 | 0,52% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Malipatil (1978) | 4 | 0,52% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Matile-Ferrero et al. (2000) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Muir (1927) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Putshkov et al. (1999) | 4 | 0,52% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Stål (1859) | 4 | 0,52% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Tuthill (1956) | 4 | 0,52% | 4 | 0,9% | 4 | 0,94% | 4 | 0,93% |
Boulard (1979) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Boulard (1995) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Cassis & Gross (2002) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Cohic (1950) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Dolling (1995) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Haupt (1927) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Herring (1961) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Herring (1965) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Hungerford (1939) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Knight (1983) | 3 | 0,39% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lallemand (1944) | 3 | 0,39% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Lupoli (2023) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Mary (2017) | 3 | 0,39% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Mifsud et al. (2010) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Nielson (1975) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Quilici et al. (1988) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Staddon (1997) | 3 | 0,39% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Yang (1935) | 3 | 0,39% | 3 | 0,68% | 3 | 0,7% | 3 | 0,7% |
Asche (1998) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Borkhsenius (1958) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Boyer de Fonscolombe (1834) | 2 | 0,26% | 1 | 0,23% | 1 | 0,23% | 0 | 0% |
Cairaschi (1941) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Chebbah et al. (2023) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Cockerell (1893) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Dadant & Etienne (1973) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Dellapé & Malipatil (2012) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Duay et al. (2014) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Geoffroy (1762) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Gross (1960) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Guilbert (2002) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Hartmann et al. (2021) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Heiss (1999) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Hempel (1902) | 2 | 0,26% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Horváth (1914) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2018) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Knight & Webb (1993) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Kormilev (1967) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Lis (1997) | 2 | 0,26% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lis (1999) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Lupoli & Abadie (2015) | 2 | 0,26% | 2 | 0,45% | 1 | 0,23% | 1 | 0,23% |
Lupoli & Dusoulier (2015) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Mamet (1959) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Maskell (1893) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Matile-Ferrero & Etienne (1998) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Olivier (1791-[1792]) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit et al. (2007) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Polhemus & Herring (1970) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Polhemus & Polhemus (1995) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Polhemus (2002) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Rageau (1958) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Rageau (1959) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Ramage & Gourvès (2017) | 2 | 0,26% | 2 | 0,45% | 1 | 0,23% | 1 | 0,23% |
Russell (1958) | 2 | 0,26% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Taquet et al. (2019) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Votýpka et al. (2020) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Williams & Watson (1988) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2023) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Zheng & Slater (1984) | 2 | 0,26% | 2 | 0,45% | 2 | 0,47% | 2 | 0,46% |
Abraham (2022) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Aguin-pombo et al. (2007) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Asche & Wilson (1990) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Balachowsky (1958) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bencheton et al. (2011) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Berenger & Pluot-Sigwalt (2017) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bigot (1992) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Biondi et al. (2013) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bondar (1923) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Bout et al. (2021) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Brunhes (1979) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Callot (2021) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Carvalho (1979) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Cassis & Vanags (2006) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Chebbah et al. (2021) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Cheesman (1927) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
China & Usinger (1950) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Cochard et al. (2021) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Cochereau (1966) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Cockerell (1895) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Conjard et al. (2022) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Davis (1909) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dedryver et al. (2009) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Disney & Chazeau (1990) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dispons (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Dominique (1892) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Duffels (1988) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dumbleton (1961) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dupuis (1999) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Duquef (2016) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Duquef (2017) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Etienne & Matile-Ferrero (2008) | 1 | 0,13% | 1 | 0,23% | 0 | 0% | 1 | 0,23% |
Etienne (1978) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Fabres (1977) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Fabricius (1775) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius ([1777]) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1803) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Fennah (1963) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferris (1935) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Frenot et al. (2005) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Garrouste & Cheng (2009) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Garrouste (2015) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Garrouste (2019) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Germain & Chapin (2004) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Germain & Streito (2004) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Germain et al. (2007) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Germain (2013) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Goux (1937) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 0 | 0% |
Grandgirard et al. (2006) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilbert (2008) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Hempel (1901) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Henry (2012) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Horváth (1908) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Hullé & Vernon (2021) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Hullé et al. (2003) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Kóbor (2020) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Kormilev (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kreiter et al. (2022) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Leavengood et al. (2024) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lis (1994) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lowe et al. (2007) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lucas (1872) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli (2019) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Malausa & Ehanno (1988) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Matile-Ferrero & Etienne (1996) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Matsumura (1912) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Maurel (2016) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Metcalf (1943) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Metcalf (1955) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrouzier (1855) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Morgan (1889) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mound & Halsey (1978) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Newstead (1909) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Nieser & Chen (2005) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ouvrard et al. (2016) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Polhemus & Herring (1970) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Polhemus & Polhemus (2008) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Polhemus (2001) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Putshkov (1987) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Rageau (1956) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Ramage et al. (2023) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Sakakibara (2002) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Sauvion et al. (1999) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Takahashi (1934) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Takiya et al. (2006) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Tatarnic & Cassis (2008) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Tatarnic & Cassis (2013) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Thomas (1994) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2018) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Tuthill (1955) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Unruh & Gullan (2008) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandeschricke et al. (1992) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Vayssières et al. (2017) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Villiers (1962) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson et al. (2015) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Webb & Viraktamath (2004) | 1 | 0,13% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |