Mammifères marins
Mammifères marins (sens large) : inclut les espèces strictement marines (habitat 1) ou pouvant également être retrouvées en eau douce (habitat 4 = eau douce / marin), en eau saumâtre (habitat 6) ou a terre (habitat 5 = marin et terrestre)
197 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Rinaldi (2016) | 280 | 29,5% | 264 | 258,82% | 264 | 352% | 196 | 233,33% |
Estrade et al. (2016) | 210 | 22,13% | 198 | 194,12% | 198 | 264% | 147 | 175% |
Carzon et al. (2016) | 208 | 21,92% | 196 | 192,16% | 196 | 261,33% | 145 | 172,62% |
Jarrett & Shirihai (2014) | 71 | 7,48% | 65 | 63,73% | 65 | 86,67% | 48 | 57,14% |
Charrassin (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Charrassin (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Moutou (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Spitz et al. (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Thoisy & Bordin (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Urtizberea (2016) | 70 | 7,38% | 66 | 64,71% | 66 | 88% | 49 | 58,33% |
Uicn et al. (2015) | 68 | 7,17% | 63 | 61,76% | 58 | 77,33% | 48 | 57,14% |
Aulagnier (2009) | 34 | 3,58% | 31 | 30,39% | 31 | 41,33% | 18 | 21,43% |
Garrigue (2007) | 31 | 3,27% | 31 | 30,39% | 30 | 40% | 23 | 27,38% |
Bordin et al. (2021) | 30 | 3,16% | 30 | 29,41% | 30 | 40% | 20 | 23,81% |
G.E.M.M. (2012) | 26 | 2,74% | 26 | 25,49% | 26 | 34,67% | 18 | 21,43% |
Catzeflis (2012) | 24 | 2,53% | 23 | 22,55% | 23 | 30,67% | 14 | 16,67% |
Dewynter et al. (2021) | 24 | 2,53% | 24 | 23,53% | 24 | 32% | 19 | 22,62% |
Gannier (2001) | 23 | 2,42% | 23 | 22,55% | 23 | 30,67% | 15 | 17,86% |
Perrin et al. (2002) | 21 | 2,21% | 18 | 17,65% | 16 | 21,33% | 13 | 15,48% |
Kiszka et al.(2007) | 20 | 2,11% | 18 | 17,65% | 18 | 24% | 14 | 16,67% |
Shirihai (2003) | 20 | 2,11% | 16 | 15,69% | 15 | 20% | 11 | 13,1% |
Gannier (2002) | 18 | 1,9% | 18 | 17,65% | 18 | 24% | 14 | 16,67% |
Gannier (2009) | 18 | 1,9% | 18 | 17,65% | 18 | 24% | 13 | 15,48% |
Uicn et al. (2017) | 18 | 1,9% | 18 | 17,65% | 18 | 24% | 10 | 11,9% |
Gannier (2000) | 16 | 1,69% | 16 | 15,69% | 16 | 21,33% | 11 | 13,1% |
Kiszka et al. (2010) | 16 | 1,69% | 15 | 14,71% | 15 | 20% | 12 | 14,29% |
Samaran & Guinet (2009) | 16 | 1,69% | 14 | 13,73% | 12 | 16% | 10 | 11,9% |
Linnaeus (1758) | 15 | 1,58% | 5 | 4,9% | 5 | 6,67% | 2 | 2,38% |
Desbrosses & Etcheberry (1987) | 14 | 1,48% | 11 | 10,78% | 11 | 14,67% | 4 | 4,76% |
Dulau-Drouot et al. (2008) | 14 | 1,48% | 14 | 13,73% | 14 | 18,67% | 10 | 11,9% |
Laran et al. (2011) | 13 | 1,37% | 13 | 12,75% | 13 | 17,33% | 10 | 11,9% |
Boer et al. (1999) | 11 | 1,16% | 10 | 9,8% | 9 | 12% | 8 | 9,52% |
Robineau & Duhamel (2006) | 11 | 1,16% | 9 | 8,82% | 8 | 10,67% | 5 | 5,95% |
Boer (2000) | 10 | 1,05% | 8 | 7,84% | 7 | 9,33% | 4 | 4,76% |
Prévost & Mougin (1970) | 9 | 0,95% | 7 | 6,86% | 7 | 9,33% | 5 | 5,95% |
Questel (2020) | 9 | 0,95% | 9 | 8,82% | 9 | 12% | 5 | 5,95% |
Robineau (1989) | 9 | 0,95% | 5 | 4,9% | 4 | 5,33% | 3 | 3,57% |
Aulagnier et al. (2017) | 8 | 0,84% | 6 | 5,88% | 6 | 8% | 3 | 3,57% |
Questel & Le Quellec (2012) | 8 | 0,84% | 8 | 7,84% | 8 | 10,67% | 4 | 4,76% |
Rossi-santos et al. (2007) | 7 | 0,74% | 5 | 4,9% | 5 | 6,67% | 3 | 3,57% |
IUCN (2012) | 6 | 0,63% | 6 | 5,88% | 6 | 8% | 4 | 4,76% |
Boer & Simmonds (2000) | 5 | 0,53% | 4 | 3,92% | 4 | 5,33% | 4 | 4,76% |
Borsa (1997) | 5 | 0,53% | 4 | 3,92% | 3 | 4% | 2 | 2,38% |
Kasamatsu & Joyce (1995) | 5 | 0,53% | 4 | 3,92% | 3 | 4% | 4 | 4,76% |
Riccialdelli et al. (2010) | 5 | 0,53% | 3 | 2,94% | 3 | 4% | 2 | 2,38% |
Robineau (2005) | 5 | 0,53% | 5 | 4,9% | 5 | 6,67% | 1 | 1,19% |
Stewart (2014) | 5 | 0,53% | 5 | 4,9% | 0 | 0% | 5 | 5,95% |
Uicn et al. (2020) | 5 | 0,53% | 5 | 4,9% | 5 | 6,67% | 3 | 3,57% |
Zelhuber (2009) | 5 | 0,53% | 5 | 4,9% | 4 | 5,33% | 4 | 4,76% |
Berta & Churchill (2012) | 4 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Deméré (2014) | 4 | 0,42% | 4 | 3,92% | 0 | 0% | 4 | 4,76% |
Macleod et al. (2006) | 4 | 0,42% | 3 | 2,94% | 3 | 4% | 3 | 3,57% |
Matsuoka et al. (2005) | 4 | 0,42% | 4 | 3,92% | 3 | 4% | 2 | 2,38% |
Thiele et al. (1999) | 4 | 0,42% | 3 | 2,94% | 2 | 2,67% | 3 | 3,57% |
AAMP (2012) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 0 | 0% |
Ainley et al. (2007) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 2 | 2,38% |
Cottarel et al. (2013) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 3 | 3,57% |
Garrigue & Poupon (2013) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 3 | 3,57% |
Jefferson & Rosenbaum (2014) | 3 | 0,32% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Kawamura (1994) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 0 | 0% |
Kock et al. (2006) | 3 | 0,32% | 3 | 2,94% | 2 | 2,67% | 3 | 3,57% |
Laran et al. (2012) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 2 | 2,38% |
Leaper et al. (2008) | 3 | 0,32% | 3 | 2,94% | 2 | 2,67% | 3 | 3,57% |
Lorvelec et al. (2007) | 3 | 0,32% | 2 | 1,96% | 2 | 2,67% | 0 | 0% |
Samaran (2008) | 3 | 0,32% | 3 | 2,94% | 1 | 1,33% | 2 | 2,38% |
Thiele et al. (2004) | 3 | 0,32% | 3 | 2,94% | 2 | 2,67% | 2 | 2,38% |
UICN (2009) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 3 | 3,57% |
Vollmer et al. (2019) | 3 | 0,32% | 3 | 2,94% | 3 | 4% | 2 | 2,38% |
Branch et al. (2007) | 2 | 0,21% | 2 | 1,96% | 0 | 0% | 2 | 2,38% |
Cunha et al. (2015) | 2 | 0,21% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Dalebout et al. (2012) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Diaz & Cuzange (2009) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Gannier & Petiau (2006) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 0 | 0% |
Garrigue et al. (2022) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Gill & Thiele (1997) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 1 | 1,19% |
Goodall et al. (1997) | 2 | 0,21% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Kasamatsu et al. (2000) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 0 | 0% |
Leaper et al. (2008) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 1 | 1,19% |
Meynier (2016) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Oremus (2009) | 2 | 0,21% | 2 | 1,96% | 1 | 1,33% | 2 | 2,38% |
Reilly et al. (2014) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Robineau et al. (2007) | 2 | 0,21% | 2 | 1,96% | 0 | 0% | 2 | 2,38% |
Robineau (2004) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 1 | 1,19% |
Samaran & Guinet (2010) | 2 | 0,21% | 2 | 1,96% | 0 | 0% | 2 | 2,38% |
Samaran et al. (2010) | 2 | 0,21% | 2 | 1,96% | 0 | 0% | 2 | 2,38% |
Spitz et al. (2015) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 0 | 0% |
Stewart (2014) | 2 | 0,21% | 2 | 1,96% | 0 | 0% | 2 | 2,38% |
Uicn et al. (2017) | 2 | 0,21% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Van Canneytet al. (2008) | 2 | 0,21% | 2 | 1,96% | 2 | 2,67% | 2 | 2,38% |
Wursig & Wursig (1980) | 2 | 0,21% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Abril et al. (1986) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Andrew et al. (2008) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Anonyme (2023) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Baker (1977) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1985) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Best & Scott (1993) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Best et al. (1995) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Bester & Roux (1986) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Boubert et al. (2019) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Branch (2010) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Breton (2014) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Brownell & Cipriano (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brownell et al. (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruyn et al. (2006) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Budylenko (1977) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Buffrenil et al. (1989) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Caballero et al. (2007) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Carzon (2012) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Cerchio et al. (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Clapham et al. (1999) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Collectif (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cotte et al. (2001) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Crespo et al. (1997) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalebout et al. (2005) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Ersts & Rosenbaum (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Fleming & Jackson (2011) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Fordyce & Marx (2012) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Friedlaender et al. (2010) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Gill et al. (2000) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (1997) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Gray (1846) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1850) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1864) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1865) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1872) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Guinet (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Hedley et al. (2007) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Heimlich-boran (1993) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Hermann (1779) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Daszkiewicz (2001) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Jaquemet et al. (2004) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Jefferson & & Van Waerebeek (2002) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Jefferson & Barros (1997) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Jefferson et al. (1993) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Jehl et al. (1980) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Johnson & Wolman (1984) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Kasamatsu et al. (1995) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Kasamatsu et al. (1998) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Kiszka et al. (2007) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Kiszka et al. (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Krajewsky (2012) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Labach et al. (2021) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Leatherwood et al. (1979) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Lesson (1828) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Matsuoka et al. (1996) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Matsuoka et al. (2005) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Müller (1776) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Murase et al. (2002) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Nicol et al. (2000) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Niort (1950) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Okamura & Kitakado (2008) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Pallas (1776) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (1994) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Perry et al. (1999) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Peters (1875) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierpoint et al. (1997) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Pitman & Ensor (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Pool (2013) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Praderi et al. (1992) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Pusineri & Caceres (2012) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Pusineri et al. (2013) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Ribic et al. (1991) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Richards (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Ridoux (2016) | 1 | 0,11% | 1 | 0,98% | 0 | 0% | 1 | 1,19% |
Roche & Guinet (2007) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Rogers & Brown (1999) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Rosenbaum & Collins (2006) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Savouré-Soubelet et al. (2016) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Sekiguchi et al. (1992) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Sekiguchi et al. (1993) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Sekiguchi et al. (2006) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Siciliano & Santos (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Sirovic et al. (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Slater et al. (2014) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Smith et al. (2005) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Thoisy et al. (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Tougaard (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tresset et al. (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Vanwaerebeek et al. (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Viale & Frontier (1989) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Vigne (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Vincent (1987) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Wada et al. (2003) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Wang et al. (2014) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Webber (2014) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 1 | 1,19% |
Weerdt (2023) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Williams et al. (2009) | 1 | 0,11% | 1 | 0,98% | 1 | 1,33% | 0 | 0% |
Wursig et al. (2007) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |