Metadata Sub-indicator 14.3.1.1. Average marine acidity (pH) in Spanish territorial waters
Goal 14. Conserve and sustainably use the oceans, seas and marine resources for sustainable development
Target 14.3. Minimize and address the impacts of ocean acidification, including through enhanced scientific cooperation at all levels
Indicator 14.3.1. Average marine acidity (pH) measured at agreed suite of representative sampling stations
Sub-indicator 14.3.1.1. Average marine acidity (pH) in Spanish territorial waters
Defined as the average pH value measured at a representative set of sampling stations over a given period of time. The pH represents the acidity (low values) or alkalinity (high values) of a solution and, in the context of the indicator, is shown as a Total scale in-situ temperature and averaged over the year. Typical surface ocean values are currently in the range of approximately 8.0 to 8.2. Mean sea acidity is used as an indicator of the health of the marine ecosystem in the context of the ocean. The ocean's absorption of atmospheric carbon dioxide (CO2) is causing a decrease in the pH of seawater, known as ocean acidification. This process negatively impacts the calcification of marine organisms, such as corals and molluscs, and can disturb the marine food chain.
Surface pH values on the Total Scale were obtained from the Copernicus Marine Service (CMEMS) observational global product MULTIOBS_GLO_BIO_CARBON_SURFACE_MYNRT_015_008 (Chau et al., 2024a, 2024b, 2022), with a spatial resolution of 0.25º × 0.25º. This version uses the final pH data supplied by the indicated product, instead of using SOCAT pCO2 (Bakker et al., 2016) and GLODAPV2 gridded AT (Lauvset et al., 2016, Olsen et al., 2016) to derive pH as in previous version. The underlying methodology maintains thermodynamic consistency with the previous version of the indicator: pH is derived by solving the carbonate thermodynamic system from pCO2¿ (reconstructed using neural networks on SOCAT observations) and Total Alkalinity (estimated using the LIAR method). The thermodynamic calculation employs the same standard dissociation constants (Lueker et al., 2000; Perez and Fraga, 1987; Dickson, 1990; Uppström, 1974). The consistency of this approach was validated through direct participation in the scientific editing of the reference article. From the monthly grids, data falling inside the official boundaries of each marine demarcation were extracted, to generate monthly area-averaged measurements and the reported annual means.
pH value
Annual
Boundary
Tier II
No
14/11/2025
UNEP
Named references in the calculation method are:
Surface ocean carbon fields DOI: https://doi.org/10.48670/moi-00047
- Chau, T.-T.-T., Gehlen, M., Metzl, N., and Chevallier, F.: CMEMS-LSCE: a global, 0.25°, monthly reconstruction of the surface ocean carbonate system, Earth Syst. Sci. Data, 16, 121–160, https://doi.org/10.5194/essd-16-121-2024, 2024a.
- Chau, T. T. T., Gehlen, M., and Chevallier, F.: A seamless ensemble-based reconstruction of surface ocean pCO2 and air–sea CO2 fluxes over the global coastal and open oceans, Biogeosciences, 19, 1087–1109, https://doi.org/10.5194/bg-19-1087-2022, 2022.
- Chau, T.-T.-T., Chevallier, F., & Gehlen, M. (2024b). Global analysis of surface ocean CO2 fugacity and air-sea fluxes with low latency. Geophysical Research Letters, 51, e2023GL106670. https://doi.org/10.1029/2023GL106670
- Bakker, D. C. E., Pfeil, B., Landa, C. S., Metzl, N., O’Brien, K. M., Olsen, A., et al. (2016). A multi-decade record of high-quality fCO2 data in version 3 of the Surface Ocean CO2 Atlas (SOCAT). Earth Syst. Sci. Data 8, 383–413. doi: 10.5194/essd-8-383-2016.
- Dickson, A. G. (1990). Thermodynamics of the dissociation of boric acid in synthetic seawater from 273.15 to 318.15 K. Deep Sea Res. Part Oceanogr. Res. Pap. 37, 755–766.
- Lauvset, S. K., Key, R. M., Olsen, A., van Heuven, S., Velo, A., Lin, X., et al. (2016). A new global interior ocean mapped climatology: the 1ox1o GLODAP version 2. Earth Syst. Sci. Data 8, 325–340. doi: 10.5194/essd-8-325-2016.
- Lueker, T. J., Dickson, A. G., and Keeling, C. D. (2000). Ocean pCO2 calculated from dissolved inorganic carbon, alkalinity, and equations for K1 and K2: validation based on laboratory measurements of CO2 in gas and seawater at equilibrium. Mar. Chem. 70, 105–119. doi: 10.1016/S0304-4203(00)00022-0.
- Olsen, A., Key, R. M., van Heuven, S., Lauvset, S. K., Velo, A., Lin, X., et al. (2016). The Global Ocean Data Analysis Project version 2 (GLODAPv2) – an internally consistent data product for the world ocean. Earth Syst. Sci. Data 8, 297–323. doi: 10.5194/essd-8-297-2016.
- Pérez, F. F., and Fraga, F. (1987). Association constant of fluoride and hydrogen ions in seawater. Mar. Chem. 21, 161–168. doi: 10.1016/0304-4203(87)90036-3.
- Uppström, L. R. (1974). The boron/chlorinity ratio of deep-sea water from the Pacific Ocean. Deep Sea Res. Oceanogr. Abstr. 21, 161–162.
DDMMs, https://www.miteco.gob.es/es/cartografia-y-sig/ide/descargas/costas-medio-marino/demarcaciones-marinas.html