BCO-DMO ERDDAP
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reference | site | study_type | omega_AR | standardized_calcification_anom |
---|---|---|---|---|
unitless | unitless | unitless | unitless | unitless |
Albright_et_al._2008 | Florida | Laboratory | 2.2 | -0.88 |
Albright_et_al._2008 | Florida | Laboratory | 2.23 | -1.01 |
Albright_et_al._2008 | Florida | Laboratory | 2.61 | -0.53 |
Albright_et_al._2008 | Florida | Laboratory | 2.62 | 0.16 |
Albright_et_al._2008 | Florida | Laboratory | 3.1 | 0.71 |
Albright_et_al._2008 | Florida | Laboratory | 3.2 | 1.54 |
Anthony_et_al._2008 | Australia | Laboratory | 1.72 | -1.37 |
Anthony_et_al._2008 | Australia | Laboratory | 1.92 | -0.88 |
Anthony_et_al._2008 | Australia | Laboratory | 2.82 | 0.42 |
Anthony_et_al._2008 | Australia | Laboratory | 3.13 | 0.79 |
Anthony_et_al._2008 | Australia | Laboratory | 4.77 | 1.23 |
Anthony_et_al._2008 | Australia | Laboratory | 5.22 | -0.2 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -2.07 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -1.21 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.77 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.74 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.32 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.21 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.17 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.07 |
Barkley_et_al._2015 | Palau | Field | 2.3 | -0.06 |
Barkley_et_al._2015 | Palau | Field | 2.3 | 0.08 |
Barkley_et_al._2015 | Palau | Field | 2.3 | 0.41 |
Barkley_et_al._2015 | Palau | Field | 2.3 | 1.38 |
Barkley_et_al._2015 | Palau | Field | 3.7 | -1.68 |
Barkley_et_al._2015 | Palau | Field | 3.7 | -1.43 |
Barkley_et_al._2015 | Palau | Field | 3.7 | -0.83 |
Barkley_et_al._2015 | Palau | Field | 3.7 | -0.47 |
Barkley_et_al._2015 | Palau | Field | 3.7 | -0.31 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 0.29 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 0.53 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 0.74 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 1.43 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 1.56 |
Barkley_et_al._2015 | Palau | Field | 3.7 | 1.75 |
Barkley_et_al._2017 | Palau | Laboratory | 1.36 | 0.45 |
Barkley_et_al._2017 | Palau | Laboratory | 1.37 | 0.06 |
Barkley_et_al._2017 | Palau | Laboratory | 1.38 | -0.24 |
Barkley_et_al._2017 | Palau | Laboratory | 1.4 | 0.24 |
Barkley_et_al._2017 | Palau | Laboratory | 1.41 | 1.17 |
Barkley_et_al._2017 | Palau | Laboratory | 1.43 | -1.11 |
Barkley_et_al._2017 | Palau | Laboratory | 1.43 | 0.24 |
Barkley_et_al._2017 | Palau | Laboratory | 1.45 | 0.17 |
Barkley_et_al._2017 | Palau | Laboratory | 1.46 | -0.34 |
Barkley_et_al._2017 | Palau | Laboratory | 1.46 | 0.64 |
Barkley_et_al._2017 | Palau | Laboratory | 1.46 | 0.86 |
Barkley_et_al._2017 | Palau | Laboratory | 1.5 | -0.48 |
Barkley_et_al._2017 | Palau | Laboratory | 1.5 | -0.3 |
Barkley_et_al._2017 | Palau | Laboratory | 1.54 | 1.08 |
Barkley_et_al._2017 | Palau | Laboratory | 1.55 | -0.51 |
Barkley_et_al._2017 | Palau | Laboratory | 1.57 | -1.22 |
Barkley_et_al._2017 | Palau | Laboratory | 1.58 | -2.11 |
Barkley_et_al._2017 | Palau | Laboratory | 1.58 | 0.69 |
Barkley_et_al._2017 | Palau | Laboratory | 1.59 | 0.21 |
Barkley_et_al._2017 | Palau | Laboratory | 2.18 | 0.16 |
Barkley_et_al._2017 | Palau | Laboratory | 2.22 | -1.34 |
Barkley_et_al._2017 | Palau | Laboratory | 2.22 | -0.75 |
Barkley_et_al._2017 | Palau | Laboratory | 2.22 | 0.86 |
Barkley_et_al._2017 | Palau | Laboratory | 2.22 | 1.06 |
Barkley_et_al._2017 | Palau | Laboratory | 2.24 | 0.27 |
Barkley_et_al._2017 | Palau | Laboratory | 2.25 | 1.06 |
Barkley_et_al._2017 | Palau | Laboratory | 2.26 | 0.18 |
Barkley_et_al._2017 | Palau | Laboratory | 2.28 | -0.5 |
Barkley_et_al._2017 | Palau | Laboratory | 2.29 | -0.07 |
Barkley_et_al._2017 | Palau | Laboratory | 2.32 | -1.67 |
Barkley_et_al._2017 | Palau | Laboratory | 2.32 | 0.9 |
Barkley_et_al._2017 | Palau | Laboratory | 2.33 | -0.23 |
Barkley_et_al._2017 | Palau | Laboratory | 2.36 | -2.45 |
Barkley_et_al._2017 | Palau | Laboratory | 2.37 | -0.56 |
Barkley_et_al._2017 | Palau | Laboratory | 2.39 | 0.39 |
Barkley_et_al._2017 | Palau | Laboratory | 2.4 | -1.11 |
Barkley_et_al._2017 | Palau | Laboratory | 2.42 | -0.38 |
Barkley_et_al._2017 | Palau | Laboratory | 2.49 | -1.57 |
Barkley_et_al._2017 | Palau | Laboratory | 2.53 | -0.59 |
Barkley_et_al._2017 | Palau | Laboratory | 2.79 | 1.23 |
Barkley_et_al._2017 | Palau | Laboratory | 2.91 | 1.41 |
Barkley_et_al._2017 | Palau | Laboratory | 2.91 | 1.42 |
Barkley_et_al._2017 | Palau | Laboratory | 2.94 | 1.0 |
Barkley_et_al._2017 | Palau | Laboratory | 2.96 | -1.35 |
Barkley_et_al._2017 | Palau | Laboratory | 2.98 | -0.85 |
Barkley_et_al._2017 | Palau | Laboratory | 2.98 | -0.57 |
Barkley_et_al._2017 | Palau | Laboratory | 2.98 | 1.11 |
Barkley_et_al._2017 | Palau | Laboratory | 2.99 | -0.45 |
Barkley_et_al._2017 | Palau | Laboratory | 3.0 | 0.96 |
Barkley_et_al._2017 | Palau | Laboratory | 3.01 | -0.07 |
Barkley_et_al._2017 | Palau | Laboratory | 3.02 | -0.6 |
Barkley_et_al._2017 | Palau | Laboratory | 3.03 | 0.5 |
Barkley_et_al._2017 | Palau | Laboratory | 3.04 | -1.39 |
Barkley_et_al._2017 | Palau | Laboratory | 3.04 | 0.76 |
Barkley_et_al._2017 | Palau | Laboratory | 3.12 | -0.8 |
Barkley_et_al._2017 | Palau | Laboratory | 3.12 | 0.82 |
Barkley_et_al._2017 | Palau | Laboratory | 3.12 | 1.0 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -1.82 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -1.48 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -1.42 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -1.39 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.94 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.76 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.72 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.29 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.26 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.24 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | -0.2 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.05 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.21 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.45 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.49 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.55 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.63 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.74 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 0.81 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 1.24 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 1.31 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 1.4 |
Barkley_et_al._2017 | Palau | Transplant | 2.3 | 1.66 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -1.74 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -1.6 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -1.52 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -0.95 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -0.74 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -0.69 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -0.42 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | -0.27 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.05 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.16 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.17 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.17 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.24 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.31 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 0.38 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 1.08 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 1.14 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 1.23 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 1.39 |
Barkley_et_al._2017 | Palau | Transplant | 3.7 | 1.62 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -1.49 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -1.47 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -1.17 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -1.12 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -0.87 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -0.74 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -0.69 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | -0.19 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | 0.04 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | 0.46 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | 0.98 |
Comeau_et_al._2014 | Hawaii | Laboratory | 1.83 | 1.52 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -1.2 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.97 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.96 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.53 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.37 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.13 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.06 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | -0.02 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | 0.0 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | 0.06 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | 0.47 |
Comeau_et_al._2014 | Hawaii | Laboratory | 2.36 | 1.13 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.97 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.71 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.48 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.26 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.15 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.12 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.06 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | -0.06 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | 0.12 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | 0.28 |
Comeau_et_al._2014 | Hawaii | Laboratory | 3.31 | 0.43 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | -0.55 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | -0.14 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | -0.14 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 0.0 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 0.23 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 0.47 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 0.5 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 1.04 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 1.06 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 1.07 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 1.4 |
Comeau_et_al._2014 | Japan | Laboratory | 1.91 | 1.87 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | -0.95 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | -0.31 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | -0.26 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 0.34 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 0.48 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 0.61 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 0.86 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 1.18 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 1.45 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 1.69 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 2.04 |
Comeau_et_al._2014 | Japan | Laboratory | 2.36 | 2.06 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | -0.28 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 0.31 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 0.65 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 0.73 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 0.89 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.0 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.04 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.08 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.32 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.81 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.84 |
Comeau_et_al._2014 | Japan | Laboratory | 3.24 | 1.97 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -2.05 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -1.45 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -1.2 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -0.98 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -0.63 |
Comeau_et_al._2014 | Moorea | Laboratory | 1.99 | -0.36 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | -0.69 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | 0.07 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | 0.13 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | 0.17 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | 0.2 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.0 | 0.22 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.68 | -0.71 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.68 | -0.48 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.68 | -0.3 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.68 | 0.14 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.68 | 0.17 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | -1.68 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | -1.64 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | -1.17 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | -0.1 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | 0.1 |
Comeau_et_al._2014 | Moorea | Laboratory | 2.69 | 0.79 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | -0.93 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | -0.41 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | -0.35 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | -0.29 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | 0.17 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.83 | 0.26 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.85 | -1.79 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.85 | -1.03 |
Comeau_et_al._2014 | Moorea | Laboratory | 3.85 | 0.6 |
Crook_et_al_2013 | Yucatan | Field | 0.77 | -1.19 |
Crook_et_al_2013 | Yucatan | Field | 0.81 | -1.7 |
Crook_et_al_2013 | Yucatan | Field | 1.22 | -0.34 |
Crook_et_al_2013 | Yucatan | Field | 1.82 | -0.68 |
Crook_et_al_2013 | Yucatan | Field | 1.82 | -0.46 |
Crook_et_al_2013 | Yucatan | Field | 1.85 | -0.32 |
Crook_et_al_2013 | Yucatan | Field | 1.9 | 0.2 |
Crook_et_al_2013 | Yucatan | Field | 3.6 | 0.69 |
Crook_et_al_2013 | Yucatan | Field | 3.6 | 1.46 |
Crook_et_al_2013 | Yucatan | Field | 3.83 | -0.51 |
Crook_et_al_2013 | Yucatan | Field | 4.03 | -0.13 |
Crook_et_al_2013 | Yucatan | Field | 4.03 | 0.36 |
Crook_et_al_2013 | Yucatan | Field | 4.12 | 2.11 |
Crook_et_al_2013 | Yucatan | Field | 4.24 | 0.52 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -2.0 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.74 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.68 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.58 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.54 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.28 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.18 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.13 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.13 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -1.11 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.77 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.77 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.77 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.64 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.63 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.63 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.6 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.54 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.53 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.48 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.44 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.26 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.21 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.13 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | -0.12 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | 0.39 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | 0.53 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | 0.54 |
dePutron_et_al._2011 | Bermuda | Laboratory | 1.41 | 0.82 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.55 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.43 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.35 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.23 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.21 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.17 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -1.0 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.76 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.76 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.67 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.63 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.57 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.56 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.56 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.48 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.47 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.44 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.37 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.36 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.09 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | -0.06 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.02 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.08 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.11 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.16 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.2 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.22 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.26 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.34 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.49 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.57 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.59 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.6 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.62 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.63 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.74 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.74 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.77 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.86 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 0.97 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 1.37 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 1.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 2.27 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 2.41 |
dePutron_et_al._2011 | Bermuda | Laboratory | 2.84 | 2.56 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.45 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.35 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.34 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.28 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.16 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.15 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.1 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -1.0 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.95 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.92 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.87 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.87 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.86 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.84 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.84 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.83 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.8 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.71 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.7 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.7 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.67 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.46 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.41 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.41 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.4 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.36 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.34 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.32 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.28 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.23 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.23 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.16 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.11 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.08 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.07 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.07 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.07 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.04 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | -0.01 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.01 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.03 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.04 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.06 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.14 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.17 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.18 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.18 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.19 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.2 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.24 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.24 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.3 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.34 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.37 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.38 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.42 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.42 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.47 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.49 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.53 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.58 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.69 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.69 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.7 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.82 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.87 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.89 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.9 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 0.96 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.03 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.07 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.24 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.25 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.27 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.29 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.37 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.42 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.5 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.54 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.63 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.68 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.74 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 1.96 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.17 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.24 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.34 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.59 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.6 |
dePutron_et_al._2011 | Bermuda | Laboratory | 4.0 | 2.64 |
Edmunds_2012 | Moorea | Laboratory | 1.7 | -0.12 |
Edmunds_2012 | Moorea | Laboratory | 1.7 | -0.04 |
Edmunds_2012 | Moorea | Laboratory | 1.7 | 0.08 |
Edmunds_2012 | Moorea | Laboratory | 1.7 | 1.08 |
Edmunds_2012 | Moorea | Laboratory | 1.7 | 1.6 |
Edmunds_2012 | Moorea | Laboratory | 1.78 | -0.92 |
Edmunds_2012 | Moorea | Laboratory | 1.78 | -0.8 |
Edmunds_2012 | Moorea | Laboratory | 1.78 | -0.48 |
Edmunds_2012 | Moorea | Laboratory | 1.78 | 0.12 |
Edmunds_2012 | Moorea | Laboratory | 1.78 | 1.52 |
Edmunds_2012 | Moorea | Laboratory | 1.93 | -2.72 |
Edmunds_2012 | Moorea | Laboratory | 1.93 | -0.44 |
Edmunds_2012 | Moorea | Laboratory | 1.93 | 0.24 |
Edmunds_2012 | Moorea | Laboratory | 1.93 | 0.92 |
Edmunds_2012 | Moorea | Laboratory | 1.93 | 1.24 |
Edmunds_2012 | Moorea | Laboratory | 2.02 | -2.19 |
Edmunds_2012 | Moorea | Laboratory | 2.02 | -1.51 |
Edmunds_2012 | Moorea | Laboratory | 2.02 | -1.28 |
Edmunds_2012 | Moorea | Laboratory | 2.02 | -0.95 |
Edmunds_2012 | Moorea | Laboratory | 2.02 | 0.39 |
Edmunds_2012 | Moorea | Laboratory | 2.08 | -1.1 |
Edmunds_2012 | Moorea | Laboratory | 2.08 | -0.33 |
Edmunds_2012 | Moorea | Laboratory | 2.08 | -0.09 |
Edmunds_2012 | Moorea | Laboratory | 2.08 | 1.29 |
Edmunds_2012 | Moorea | Laboratory | 2.08 | 1.84 |
Edmunds_2012 | Moorea | Laboratory | 2.11 | -1.68 |
Edmunds_2012 | Moorea | Laboratory | 2.11 | -1.6 |
Edmunds_2012 | Moorea | Laboratory | 2.11 | -0.68 |
Edmunds_2012 | Moorea | Laboratory | 2.11 | -0.6 |
Edmunds_2012 | Moorea | Laboratory | 2.11 | 0.2 |
Edmunds_2012 | Moorea | Laboratory | 2.22 | -1.05 |
Edmunds_2012 | Moorea | Laboratory | 2.22 | 0.34 |
Edmunds_2012 | Moorea | Laboratory | 2.22 | 0.77 |
Edmunds_2012 | Moorea | Laboratory | 2.22 | 0.89 |
Edmunds_2012 | Moorea | Laboratory | 2.22 | 1.34 |
Edmunds_2012 | Moorea | Laboratory | 2.26 | -0.75 |
Edmunds_2012 | Moorea | Laboratory | 2.26 | -0.71 |
Edmunds_2012 | Moorea | Laboratory | 2.26 | -0.69 |
Edmunds_2012 | Moorea | Laboratory | 2.26 | 1.31 |
Edmunds_2012 | Moorea | Laboratory | 2.68 | -0.4 |
Edmunds_2012 | Moorea | Laboratory | 2.68 | -0.24 |
Edmunds_2012 | Moorea | Laboratory | 2.68 | -0.12 |
Edmunds_2012 | Moorea | Laboratory | 2.68 | 0.04 |
Edmunds_2012 | Moorea | Laboratory | 2.68 | 0.6 |
Edmunds_2012 | Moorea | Laboratory | 2.69 | -0.56 |
Edmunds_2012 | Moorea | Laboratory | 2.69 | 0.04 |
Edmunds_2012 | Moorea | Laboratory | 2.69 | 0.12 |
Edmunds_2012 | Moorea | Laboratory | 2.69 | 0.44 |
Edmunds_2012 | Moorea | Laboratory | 2.69 | 0.8 |
Edmunds_2012 | Moorea | Laboratory | 2.92 | -1.16 |
Edmunds_2012 | Moorea | Laboratory | 2.92 | 0.28 |
Edmunds_2012 | Moorea | Laboratory | 2.92 | 0.36 |
Edmunds_2012 | Moorea | Laboratory | 2.92 | 0.36 |
Edmunds_2012 | Moorea | Laboratory | 2.92 | 0.96 |
Edmunds_2012 | Moorea | Laboratory | 2.96 | -1.64 |
Edmunds_2012 | Moorea | Laboratory | 2.96 | -0.84 |
Edmunds_2012 | Moorea | Laboratory | 2.96 | 0.2 |
Edmunds_2012 | Moorea | Laboratory | 2.96 | 1.4 |
Edmunds_2012 | Moorea | Laboratory | 2.96 | 2.28 |
Edmunds_2012 | Moorea | Laboratory | 3.29 | -0.7 |
Edmunds_2012 | Moorea | Laboratory | 3.29 | -0.2 |
Edmunds_2012 | Moorea | Laboratory | 3.29 | -0.18 |
Edmunds_2012 | Moorea | Laboratory | 3.29 | 0.78 |
Edmunds_2012 | Moorea | Laboratory | 3.29 | 1.19 |
Edmunds_2012 | Moorea | Laboratory | 3.37 | -0.2 |
Edmunds_2012 | Moorea | Laboratory | 3.37 | -0.02 |
Edmunds_2012 | Moorea | Laboratory | 3.37 | 0.07 |
Edmunds_2012 | Moorea | Laboratory | 3.37 | 0.75 |
Edmunds_2012 | Moorea | Laboratory | 3.37 | 0.99 |
Enochs_et_al._2015 | Maug | Field | 3.39 | -0.58 |
Enochs_et_al._2015 | Maug | Field | 3.66 | -0.58 |
Enochs_et_al._2015 | Maug | Field | 3.84 | 1.16 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.0 | -1.25 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.0 | -1.12 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.0 | -0.41 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.5 | -0.51 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.5 | -0.44 |
Iguchi_et_al._2012 | Japan | Laboratory | 1.5 | 0.87 |
Iguchi_et_al._2012 | Japan | Laboratory | 3.5 | 0.46 |
Iguchi_et_al._2012 | Japan | Laboratory | 3.5 | 0.62 |
Iguchi_et_al._2012 | Japan | Laboratory | 3.5 | 1.79 |
Manzello_et_al._2014 | Galapagos | Field | 2.42 | -1.23 |
Manzello_et_al._2014 | Galapagos | Field | 2.83 | -0.25 |
Manzello_et_al._2014 | Galapagos | Field | 3.02 | 0.32 |
Manzello_et_al._2014 | Galapagos | Field | 3.28 | 1.15 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.08 | -1.62 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.16 | -1.58 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.37 | -0.36 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.61 | 0.44 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.68 | -1.28 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.8 | -1.43 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.81 | -1.43 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.82 | -1.24 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.82 | -1.03 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.9 | -0.46 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 1.95 | -0.51 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 2.1 | 0.02 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 2.33 | -1.07 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 2.6 | -1.72 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 2.86 | -0.3 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.15 | 0.78 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.53 | -0.67 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.65 | -0.59 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.69 | -0.74 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.74 | -0.48 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.75 | 0.25 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 3.83 | 0.15 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 4.01 | 0.59 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 4.07 | 1.18 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 4.24 | -0.11 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 4.61 | -0.59 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 4.98 | -0.32 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.0 | 0.29 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.02 | 1.6 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.13 | -0.38 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.25 | 0.44 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.27 | 1.09 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.3 | -0.36 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.31 | 1.51 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.52 | 1.13 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.58 | 0.92 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 5.78 | 0.17 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 6.17 | -0.21 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 6.34 | 2.75 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 6.4 | 1.18 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 6.94 | 0.27 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 7.21 | 1.64 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 7.26 | 0.0 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 7.27 | 0.63 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 7.36 | 0.44 |
Ohde_and_Hossain_2004 | Japan | Laboratory | 7.56 | 1.01 |