Editing Specification report of common test protocols and intercomparison methodologies

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=Rationales: the pCO<sub>2</sub> Use case=
 
=Rationales: the pCO<sub>2</sub> Use case=
  
The ocean absorbs about 25 % of anthropogenic carbon dioxide (CO<sub>2</sub>) emissions, moderating the rate and severity of climate change. Such massive input of CO<sub>2</sub> generates sweeping changes in the chemistry of the carbon system, including an increase in dissolved inorganic carbon (CT) and bicarbonates (HCO<sub>3</sub><sup>–</sup>) as well as a decrease in pH and in the concentration of carbonate (CO<sub>3</sub><sup>2–</sup>) ions. These changes are collectively referred to as "ocean acidification". The pH of ocean surface water has decreased by 0.1 units since the beginning of the industrial era, corresponding to a 26 % increase in hydrogen ion concentration, and the total decrease by 2100 will range from 0.14 to 0.4 units. These changes are, however, quite variable regionally and with depth. Elucidating the biological, ecological, biogeochemical and societal consequences of ocean acidification therefore requires a fine resolution of ocean CO<sub>2</sub> data in space and time. Thus, humankind is in urgent need of routine and sustained global information on the marine environment sufficient to meet society's needs for describing, understanding and forecasting variability and long-term change. We do know, however, that significant marine CO<sub>2</sub> sources and sinks exist in currently under sampled or even unsampled areas, which are undergoing rapid anthropogenically driven change and exhibit high vulnerability (e.g., increasingly ice-free Arctic Ocean, Southern Ocean, coastal seas).
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The ocean absorbs about 25 % of anthropogenic carbon dioxide (CO<sub>2</sub>) emissions, moderating the rate and severity of climate change. Such massive input of CO2 generates sweeping changes in the chemistry of the carbon system, including an increase in dissolved inorganic carbon (CT) and bicarbonates (HCO<sub>3</sub><sup>–</sup>) as well as a decrease in pH and in the concentration of carbonate (CO<sub>3</sub><sup>2–</sup>) ions. These changes are collectively referred to as "ocean acidification". The pH of ocean surface water has decreased by 0.1 units since the beginning of the industrial era, corresponding to a 26 % increase in hydrogen ion concentration, and the total decrease by 2100 will range from 0.14 to 0.4 units. These changes are, however, quite variable regionally and with depth. Elucidating the biological, ecological, biogeochemical and societal consequences of ocean acidification therefore requires a fine resolution of ocean CO2 data in space and time. Thus, humankind is in urgent need of routine and sustained global information on the marine environment sufficient to meet society's needs for describing, understanding and forecasting variability and long-term change. We do know, however, that significant marine CO2 sources and sinks exist in currently under sampled or even unsampled areas, which are undergoing rapid anthropogenically driven change and exhibit high vulnerability (e.g., increasingly ice-free Arctic Ocean, Southern Ocean, coastal seas).
  
 
The situation at sea surface is monitored on long term time series in sparse places of the global ocean, by using repeated oceanographic cruises where ships are equipped with surface continuum pCO<sub>2</sub> sampling systems. The produced data can be directly compared to atmospheric measurements of the pCO<sub>2</sub> concentration to assess the flux of inorganic carbon from atmosphere to ocean.
 
The situation at sea surface is monitored on long term time series in sparse places of the global ocean, by using repeated oceanographic cruises where ships are equipped with surface continuum pCO<sub>2</sub> sampling systems. The produced data can be directly compared to atmospheric measurements of the pCO<sub>2</sub> concentration to assess the flux of inorganic carbon from atmosphere to ocean.

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