Mammifères marins de France
Mammifères marins (sens large) de France (métropole et outre-mer) : 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).
192 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) | 276 | 29,55% | 260 | 265,31% | 260 | 366,2% | 192 | 240% |
| Estrade et al. (2016) | 207 | 22,16% | 195 | 198,98% | 195 | 274,65% | 144 | 180% |
| Carzon et al. (2016) | 205 | 21,95% | 193 | 196,94% | 193 | 271,83% | 142 | 177,5% |
| Jarrett & Shirihai (2014) | 71 | 7,6% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Charrassin (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Charrassin (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Moutou (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Spitz et al. (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Thoisy & Bordin (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Urtizberea (2016) | 69 | 7,39% | 65 | 66,33% | 65 | 91,55% | 48 | 60% |
| Uicn et al. (2015) | 68 | 7,28% | 63 | 64,29% | 58 | 81,69% | 48 | 60% |
| Aulagnier (2009) | 33 | 3,53% | 30 | 30,61% | 30 | 42,25% | 17 | 21,25% |
| Garrigue (2007) | 31 | 3,32% | 31 | 31,63% | 30 | 42,25% | 23 | 28,75% |
| Bordin et al. (2021) | 30 | 3,21% | 30 | 30,61% | 30 | 42,25% | 20 | 25% |
| G.E.M.M. (2012) | 25 | 2,68% | 25 | 25,51% | 25 | 35,21% | 17 | 21,25% |
| Catzeflis (2012) | 24 | 2,57% | 23 | 23,47% | 23 | 32,39% | 14 | 17,5% |
| Dewynter et al. (2021) | 23 | 2,46% | 23 | 23,47% | 23 | 32,39% | 18 | 22,5% |
| Gannier (2001) | 23 | 2,46% | 23 | 23,47% | 23 | 32,39% | 15 | 18,75% |
| Perrin et al. (2002) | 21 | 2,25% | 18 | 18,37% | 16 | 22,54% | 13 | 16,25% |
| Shirihai (2003) | 20 | 2,14% | 16 | 16,33% | 15 | 21,13% | 11 | 13,75% |
| Gannier (2002) | 18 | 1,93% | 18 | 18,37% | 18 | 25,35% | 14 | 17,5% |
| Gannier (2009) | 18 | 1,93% | 18 | 18,37% | 18 | 25,35% | 13 | 16,25% |
| Kiszka et al.(2007) | 18 | 1,93% | 16 | 16,33% | 16 | 22,54% | 12 | 15% |
| Uicn et al. (2017) | 18 | 1,93% | 18 | 18,37% | 18 | 25,35% | 10 | 12,5% |
| Gannier (2000) | 16 | 1,71% | 16 | 16,33% | 16 | 22,54% | 11 | 13,75% |
| Kiszka et al. (2010) | 16 | 1,71% | 15 | 15,31% | 15 | 21,13% | 12 | 15% |
| Samaran & Guinet (2009) | 16 | 1,71% | 14 | 14,29% | 12 | 16,9% | 10 | 12,5% |
| Linnaeus (1758) | 15 | 1,61% | 5 | 5,1% | 5 | 7,04% | 2 | 2,5% |
| Desbrosses & Etcheberry (1987) | 14 | 1,5% | 11 | 11,22% | 11 | 15,49% | 4 | 5% |
| Dulau-Drouot et al. (2008) | 14 | 1,5% | 14 | 14,29% | 14 | 19,72% | 10 | 12,5% |
| Laran et al. (2011) | 13 | 1,39% | 13 | 13,27% | 13 | 18,31% | 10 | 12,5% |
| Boer et al. (1999) | 11 | 1,18% | 10 | 10,2% | 9 | 12,68% | 8 | 10% |
| Robineau & Duhamel (2006) | 11 | 1,18% | 9 | 9,18% | 8 | 11,27% | 5 | 6,25% |
| Boer (2000) | 10 | 1,07% | 8 | 8,16% | 7 | 9,86% | 4 | 5% |
| Prévost & Mougin (1970) | 9 | 0,96% | 7 | 7,14% | 7 | 9,86% | 5 | 6,25% |
| Questel (2020) | 9 | 0,96% | 9 | 9,18% | 9 | 12,68% | 5 | 6,25% |
| Robineau (1989) | 9 | 0,96% | 5 | 5,1% | 4 | 5,63% | 3 | 3,75% |
| Questel & Le Quellec (2012) | 8 | 0,86% | 8 | 8,16% | 8 | 11,27% | 4 | 5% |
| Aulagnier et al. (2017) | 7 | 0,75% | 5 | 5,1% | 5 | 7,04% | 2 | 2,5% |
| Rossi-santos et al. (2007) | 7 | 0,75% | 5 | 5,1% | 5 | 7,04% | 3 | 3,75% |
| Boer & Simmonds (2000) | 5 | 0,54% | 4 | 4,08% | 4 | 5,63% | 4 | 5% |
| Borsa (1997) | 5 | 0,54% | 4 | 4,08% | 3 | 4,23% | 2 | 2,5% |
| IUCN (2012) | 5 | 0,54% | 5 | 5,1% | 5 | 7,04% | 3 | 3,75% |
| Kasamatsu & Joyce (1995) | 5 | 0,54% | 4 | 4,08% | 3 | 4,23% | 4 | 5% |
| Riccialdelli et al. (2010) | 5 | 0,54% | 3 | 3,06% | 3 | 4,23% | 2 | 2,5% |
| Robineau (2005) | 5 | 0,54% | 5 | 5,1% | 5 | 7,04% | 1 | 1,25% |
| Stewart (2014) | 5 | 0,54% | 5 | 5,1% | 0 | 0% | 5 | 6,25% |
| Uicn et al. (2020) | 5 | 0,54% | 5 | 5,1% | 5 | 7,04% | 3 | 3,75% |
| Zelhuber (2009) | 5 | 0,54% | 5 | 5,1% | 4 | 5,63% | 4 | 5% |
| Berta & Churchill (2012) | 4 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Deméré (2014) | 4 | 0,43% | 4 | 4,08% | 0 | 0% | 4 | 5% |
| Macleod et al. (2006) | 4 | 0,43% | 3 | 3,06% | 3 | 4,23% | 3 | 3,75% |
| Matsuoka et al. (2005) | 4 | 0,43% | 4 | 4,08% | 3 | 4,23% | 2 | 2,5% |
| Thiele et al. (1999) | 4 | 0,43% | 3 | 3,06% | 2 | 2,82% | 3 | 3,75% |
| AAMP (2012) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 0 | 0% |
| Ainley et al. (2007) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 2 | 2,5% |
| Cottarel et al. (2013) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 3 | 3,75% |
| Garrigue & Poupon (2013) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 3 | 3,75% |
| Jefferson & Rosenbaum (2014) | 3 | 0,32% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Kawamura (1994) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 0 | 0% |
| Kock et al. (2006) | 3 | 0,32% | 3 | 3,06% | 2 | 2,82% | 3 | 3,75% |
| Laran et al. (2012) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 2 | 2,5% |
| Leaper et al. (2008) | 3 | 0,32% | 3 | 3,06% | 2 | 2,82% | 3 | 3,75% |
| Samaran (2008) | 3 | 0,32% | 3 | 3,06% | 1 | 1,41% | 2 | 2,5% |
| Thiele et al. (2004) | 3 | 0,32% | 3 | 3,06% | 2 | 2,82% | 2 | 2,5% |
| UICN (2009) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 3 | 3,75% |
| Vollmer et al. (2019) | 3 | 0,32% | 3 | 3,06% | 3 | 4,23% | 2 | 2,5% |
| Branch et al. (2007) | 2 | 0,21% | 2 | 2,04% | 0 | 0% | 2 | 2,5% |
| Cunha et al. (2015) | 2 | 0,21% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Diaz & Cuzange (2009) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 0 | 0% |
| Fourt et al. (2017) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Gannier & Petiau (2006) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 0 | 0% |
| Garrigue et al. (2022) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Gill & Thiele (1997) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 1 | 1,25% |
| Goodall et al. (1997) | 2 | 0,21% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Kasamatsu et al. (2000) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 0 | 0% |
| Leaper et al. (2008) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 1 | 1,25% |
| Lorvelec et al. (2007) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 0 | 0% |
| Meynier (2016) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Oremus (2009) | 2 | 0,21% | 2 | 2,04% | 1 | 1,41% | 2 | 2,5% |
| Reilly et al. (2014) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Robineau et al. (2007) | 2 | 0,21% | 2 | 2,04% | 0 | 0% | 2 | 2,5% |
| Robineau (2004) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 1 | 1,25% |
| Samaran & Guinet (2010) | 2 | 0,21% | 2 | 2,04% | 0 | 0% | 2 | 2,5% |
| Samaran et al. (2010) | 2 | 0,21% | 2 | 2,04% | 0 | 0% | 2 | 2,5% |
| Spitz et al. (2015) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 0 | 0% |
| Stewart (2014) | 2 | 0,21% | 2 | 2,04% | 0 | 0% | 2 | 2,5% |
| Uicn et al. (2017) | 2 | 0,21% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Van Canneytet al. (2008) | 2 | 0,21% | 2 | 2,04% | 2 | 2,82% | 2 | 2,5% |
| Wursig & Wursig (1980) | 2 | 0,21% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Abril et al. (1986) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Andrew et al. (2008) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Anonyme. (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Anonyme. (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Anonyme (2023) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Baker (1977) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baker (1985) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Best & Scott (1993) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Best et al. (1995) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Bester & Roux (1986) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Boubert et al. (2019) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Branch (2010) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Breton (2014) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 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 | 1,02% | 1 | 1,41% | 0 | 0% |
| Budylenko (1977) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Buffrenil et al. (1989) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Caballero et al. (2007) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Carzon (2012) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Cerchio et al. (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Clapham et al. (1999) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Collectif (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Collet & Duguy (1981) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cotte et al. (2001) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Counihan et al. (2012) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Crespo et al. (1997) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dalebout et al. (2005) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Ersts & Rosenbaum (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Fleming & Jackson (2011) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Fordyce & Marx (2012) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Friedlaender et al. (2010) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Gill et al. (2000) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gillespie (1997) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Gray (1846) | 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 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Guinet (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Hedley et al. (2007) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Heimlich-boran (1993) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Hoff & Daszkiewicz (2001) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Jaquemet et al. (2004) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Jefferson & & Van Waerebeek (2002) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jefferson & Barros (1997) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Jefferson et al. (1993) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Jehl et al. (1980) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Johnson & Wolman (1984) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Kasamatsu et al. (1995) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Kasamatsu et al. (1998) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Kiszka et al. (2007) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Kiszka et al. (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Krajewsky (2012) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Labach et al. (2021) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Leatherwood et al. (1979) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Lesson (1828) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Mahé et al. (2024) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Matsuoka et al. (1996) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Matsuoka et al. (2005) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Müller (1776) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murase et al. (2002) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Nicol et al. (2000) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Niort (1950) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Okamura & Kitakado (2008) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Pallas (1776) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrin et al. (1994) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Perry et al. (1999) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Peters (1875) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pierpoint et al. (1997) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Pitman & Ensor (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Pool (2013) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Praderi et al. (1992) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Pusineri & Caceres (2012) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Pusineri et al. (2013) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Ribic et al. (1991) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Richards (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Ridoux (2016) | 1 | 0,11% | 1 | 1,02% | 0 | 0% | 1 | 1,25% |
| Roche & Guinet (2007) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Rogers & Brown (1999) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Rosenbaum & Collins (2006) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Sekiguchi et al. (1992) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Sekiguchi et al. (1993) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Sekiguchi et al. (2006) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siciliano & Santos (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Sirovic et al. (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Smith et al. (2005) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Thoisy et al. (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Tougaard (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tresset et al. (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Vanwaerebeek et al. (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Viale & Frontier (1989) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Vincent (1987) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Wada et al. (2003) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Wang et al. (2014) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Webber (2014) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 1 | 1,25% |
| Weerdt (2023) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Williams et al. (2009) | 1 | 0,11% | 1 | 1,02% | 1 | 1,41% | 0 | 0% |
| Wursig et al. (2007) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
