Lawson et al. (1996) [3] | 11 | 12–17 | 0.8 | 100 | 75 | 45 | 79–930 | 2.64–4.2 | NA | NA |
Hannan et al. (1999) [5] | 33 | 9–19 | 1.1 | 94 | 27 | 42 | 27–1,700 | 2.55–4.55 | 3 | NA |
Kollars et al. (2005) [1] | 52 | 4–18 | 0.67 | 65 | 34 | 33 | 19–1,700 | 2.5–4.0 | 7 | NA |
Venail et al. (2007) [4] | 4 | 7–14 | 0.33 | 100 | 50 | 50 | 87–1,580 | 2.96–4.34 | 0 | 50 |
Libansky et al. (2008) [12] | 10 | 10–17 | 1 | 100 | 30 | 50 | 83–547 | 2.78–3.64 | 10 | NA |
Bhadada et al. (2008) [6] | 11 | 5–18 | 0.57 | 91 | 91 | 50 | 128–2,085 | 2.12–3.40 | 14 | 77 |
Mallet et al. (2008) [2] | 44 | 6–18 | 0.69 | 66 | 16 | 41 | 56–2,214 | 2.5–4.33 | NA | NA |
George et al. (2010) [7] | 18 | 10–18 | 0.29 | 100 | 89 | 39 | 80 + 66 | 3.35 + 0.49 | 5.5 | 28 |
Durkin et al. (2010) [9] | 12 | 10–18 | 0.09 | 75 | NA | 25 | 77–300 | 2.73–3.98 | 0 | NA |
Li et al. (2012) [8] | 12 | 9–16 | 0.71 | 100 | 92 | 75 | 105–2,800 | 3.25–5 | 8 | NA |