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Perfluorinated compounds are ubiquitous. Approximately 4,700 PFAS have been identified to date. Some examples of these products include carpets, glass, paper, clothing, and other textiles, cookware, food packaging, electronics, and personal care products. PFAS have been used in industrial and consumer products since the 1950s due to their physical and chemical properties. PFAS molecules can include oxygen, hydrogen, sulphur, and/or nitrogen atoms, whereas perfluorocarbon molecules contain only carbon and fluorine atoms. Perfluorinated compounds (PFAS) contain a fully fluorinated hydrophobic linear carbon chain attached to one or more hydrophilic head groups. The carbon-fluorine bond is so strong that these chemicals do not degrade in the environment. They are often referred to as ‘forever chemicals’. Some PFAS have been linked to an increased risk of cancer, high cholesterol, reproductive disorders, hormonal disruption or endocrine disruption, and weakening of the immune system. Currently, two PFAS are restricted under the international Stockholm Convention on POPs and the EU POPs Regulation. PFOS (perfluoroctanesulfonic acid) and its derivatives have been restricted since 2009/2010. PFOA (perfluorooctanoic acid), its salts, and related compounds are also regulated as of 4th July 2020. Over the past decades, global manufacturers have started to substitute long-chain PFAS with shorter-chain PFAS or with non-fluorinated substances. This trend has been driven by the fact that the undesired effects of long-chain PFAS on human health and the environment were assessed and recognised first by scientists and authorities around the globe. However short-chain PFAS are now thought to have similar or other properties of concern such as fluorinated compounds like Gen X and ADONA. The combined effects of PFAS are not widely studied and relatively unknown. There is also little biological assessment currently done for drinking water and especially marine water. These are both resea

Perfluorinated compounds are ubiquitous. Approximately 4,700 PFAS have been identified to date. Some examples of these products include carpets, glass, paper, clothing, and other textiles, cookware, food packaging, electronics, and personal care products. PFAS have been used in industrial and consumer products since the 1950s due to their physical and chemical properties. PFAS molecules can include oxygen, hydrogen, sulphur, and/or nitrogen atoms, whereas perfluorocarbon molecules contain only carbon and fluorine atoms. Perfluorinated compounds (PFAS) contain a fully fluorinated hydrophobic linear carbon chain attached to one or more hydrophilic head groups. The carbon-fluorine bond is so strong that these chemicals do not degrade in the environment. They are often referred to as ‘forever chemicals’. Some PFAS have been linked to an increased risk of cancer, high cholesterol, reproductive disorders, hormonal disruption or endocrine disruption, and weakening of the immune system. Currently, two PFAS are restricted under the international Stockholm Convention on POPs and the EU POPs Regulation. PFOS (perfluoroctanesulfonic acid) and its derivatives have been restricted since 2009/2010. PFOA (perfluorooctanoic acid), its salts, and related compounds are also regulated as of 4th July 2020. Over the past decades, global manufacturers have started to substitute long-chain PFAS with shorter-chain PFAS or with non-fluorinated substances. This trend has been driven by the fact that the undesired effects of long-chain PFAS on human health and the environment were assessed and recognised first by scientists and authorities around the globe. However short-chain PFAS are now thought to have similar or other properties of concern such as fluorinated compounds like Gen X and ADONA. The combined effects of PFAS are not widely studied and relatively unknown. There is also little biological assessment currently done for drinking water and especially marine water. These are both resea

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Perfluorinated compounds are ubiquitous. Approximately 4,700 PFAS have been identified to date. Some examples of these products include carpets, glass, paper, clothing, and other textiles, cookware, food packaging, electronics, and personal care products. PFAS have been used in industrial and consumer products since the 1950s due to their physical and chemical properties. PFAS molecules can include oxygen, hydrogen, sulphur, and/or nitrogen atoms, whereas perfluorocarbon molecules contain only carbon and fluorine atoms. Perfluorinated compounds (PFAS) contain a fully fluorinated hydrophobic linear carbon chain attached to one or more hydrophilic head groups. The carbon-fluorine bond is so strong that these chemicals do not degrade in the environment. They are often referred to as ‘forever chemicals’. Some PFAS have been linked to an increased risk of cancer, high cholesterol, reproductive disorders, hormonal disruption or endocrine disruption, and weakening of the immune system. Currently, two PFAS are restricted under the international Stockholm Convention on POPs and the EU POPs Regulation. PFOS (perfluoroctanesulfonic acid) and its derivatives have been restricted since 2009/2010. PFOA (perfluorooctanoic acid), its salts, and related compounds are also regulated as of 4th July 2020. Over the past decades, global manufacturers have started to substitute long-chain PFAS with shorter-chain PFAS or with non-fluorinated substances. This trend has been driven by the fact that the undesired effects of long-chain PFAS on human health and the environment were assessed and recognised first by scientists and authorities around the globe. However short-chain PFAS are now thought to have similar or other properties of concern such as fluorinated compounds like Gen X and ADONA. The combined effects of PFAS are not widely studied and relatively unknown. There is also little biological assessment currently done for drinking water and especially marine water. These are both resea

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

Identification of local and regional impacts of oxygen, heat and pH related “Extreme Marine Events”: Ocean model data products are overlaid with existing marine biological datasets to identify sensitive areas and organism vulnerabilities.

According to Commission Decision (EU) 2017/848 under the Marine Strategy Framework Directive (MSFD), EU Member States (MS) shall consider, in their Descriptor 8 primary criterion (D8C1) assessments, the WFD Priority Substances (PS) and River Basin Specific Pollutants (RBSP) within coastal and territorial waters and also beyond territorial waters if these still may give rise to pollution effects. Some WFD PS might not be relevant for the marine environment in the open sea and, consequently, might be excluded from MSFD monitoring beyond the territorial waters. MS have expressed the need for a framework for the deselection of WFD PS from monitoring under the MSFD, in order to save resources. The European Commission’s Joint Research Centre (JRC), collaborating within the MSFD Expert Network on Contaminants, has developed a pragmatic approach to identify the WFD PS that can be excluded from MSFD monitoring in the open sea beyond territorial waters without reducing protection of European Seas. This should preempt the need for individual MS to provide rationales for such exclusions, support comparable monitoring and assessments across national boundaries, and enable MS to focus their monitoring efforts on other (including emerging) substances that require attention.

According to Commission Decision (EU) 2017/848 under the Marine Strategy Framework Directive (MSFD), EU Member States (MS) shall consider, in their Descriptor 8 primary criterion (D8C1) assessments, the WFD Priority Substances (PS) and River Basin Specific Pollutants (RBSP) within coastal and territorial waters and also beyond territorial waters if these still may give rise to pollution effects. Some WFD PS might not be relevant for the marine environment in the open sea and, consequently, might be excluded from MSFD monitoring beyond the territorial waters. MS have expressed the need for a framework for the deselection of WFD PS from monitoring under the MSFD, in order to save resources. The European Commission’s Joint Research Centre (JRC), collaborating within the MSFD Expert Network on Contaminants, has developed a pragmatic approach to identify the WFD PS that can be excluded from MSFD monitoring in the open sea beyond territorial waters without reducing protection of European Seas. This should preempt the need for individual MS to provide rationales for such exclusions, support comparable monitoring and assessments across national boundaries, and enable MS to focus their monitoring efforts on other (including emerging) substances that require attention.

According to Commission Decision (EU) 2017/848 under the Marine Strategy Framework Directive (MSFD), EU Member States (MS) shall consider, in their Descriptor 8 primary criterion (D8C1) assessments, the WFD Priority Substances (PS) and River Basin Specific Pollutants (RBSP) within coastal and territorial waters and also beyond territorial waters if these still may give rise to pollution effects. Some WFD PS might not be relevant for the marine environment in the open sea and, consequently, might be excluded from MSFD monitoring beyond the territorial waters. MS have expressed the need for a framework for the deselection of WFD PS from monitoring under the MSFD, in order to save resources. The European Commission’s Joint Research Centre (JRC), collaborating within the MSFD Expert Network on Contaminants, has developed a pragmatic approach to identify the WFD PS that can be excluded from MSFD monitoring in the open sea beyond territorial waters without reducing protection of European Seas. This should preempt the need for individual MS to provide rationales for such exclusions, support comparable monitoring and assessments across national boundaries, and enable MS to focus their monitoring efforts on other (including emerging) substances that require attention.

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO(2)) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 +/- 4.7 Tg C yr(-1) over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO(2) gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 +/- 3.1 Tg C yr(-1), while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 +/- 6.0 Tg C yr(-1)).

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO(2)) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 +/- 4.7 Tg C yr(-1) over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO(2) gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 +/- 3.1 Tg C yr(-1), while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 +/- 6.0 Tg C yr(-1)).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermallydriven, air-sea fCO 2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO(2)) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 +/- 4.7 Tg C yr(-1) over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO(2) gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 +/- 3.1 Tg C yr(-1), while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 +/- 6.0 Tg C yr(-1)).

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermallydriven, air-sea fCO 2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

Four contrasting coastal systems in Ireland, each with shellfish production activities, were studied to provide a first evaluation of the spatial and seasonal influences on the local carbonate system. The study sites included; (1) a coastal system with sandstone bedrock and minimal freshwater sources, (2) an estuarine system with a catchment limestone bedrock, (3) an estuarine system with a catchment granite bedrock, and (4) a karst groundwater-fed estuary. The type of bedrock was the dominant control on regional carbonate chemistry, where the calcium carbonate catchment bedrock was a strong source of both dissolved inorganic carbon and total alkalinity input in the two limestone regions, which are supersaturated with respect to atmospheric CO2 throughout the year. Primary production played an important role in the non-limestone regions, where both systems were CO2-undersaturated during productive months. Minimum aragonite saturation () was observed at all sites during winter when productivity is lowest; surface winter is <1.5 close to the mussel farms in Kinvara Bay and Bantry Bay. was recalculated to account for the higher calcium concentrations in the River Suir from limestone dissolution, which increases by 0.5 in the mid estuary and >2 in the inner estuary. The substrate-to-inhibitor ratio (SIR), an alternative indicator of ecosystem vulnerability to acidification, was positively correlated to in all systems, however with more variability in the two limestone regions. Results highlight challenges of assessing local ecosystem vulnerability to future acidification and the importance of understanding the local spatio-temporal biogeochemistry.

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth's climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo's unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO(2)) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 +/- 4.7 Tg C yr(-1) over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO(2) gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 +/- 3.1 Tg C yr(-1), while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 +/- 6.0 Tg C yr(-1)).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth’s climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo’s unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

Four contrasting coastal systems in Ireland, each with shellfish production activities, were studied to provide a first evaluation of the spatial and seasonal influences on the local carbonate system. The study sites included; (1) a coastal system with sandstone bedrock and minimal freshwater sources, (2) an estuarine system with a catchment limestone bedrock, (3) an estuarine system with a catchment granite bedrock, and (4) a karst groundwater-fed estuary. The type of bedrock was the dominant control on regional carbonate chemistry, where the calcium carbonate catchment bedrock was a strong source of both dissolved inorganic carbon and total alkalinity input in the two limestone regions, which are supersaturated with respect to atmospheric CO2 throughout the year. Primary production played an important role in the non-limestone regions, where both systems were CO2-undersaturated during productive months. Minimum aragonite saturation () was observed at all sites during winter when productivity is lowest; surface winter is <1.5 close to the mussel farms in Kinvara Bay and Bantry Bay. was recalculated to account for the higher calcium concentrations in the River Suir from limestone dissolution, which increases by 0.5 in the mid estuary and >2 in the inner estuary. The substrate-to-inhibitor ratio (SIR), an alternative indicator of ecosystem vulnerability to acidification, was positively correlated to in all systems, however with more variability in the two limestone regions. Results highlight challenges of assessing local ecosystem vulnerability to future acidification and the importance of understanding the local spatio-temporal biogeochemistry.

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth's climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo's unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth's climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo's unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

The Global Ocean Ship-Based Hydrographic Investigations Program (GO-SHIP) provides a globally coordinated network and oversight of 55 sustained decadal repeat hydrographic reference lines. GO-SHIP is part of the global ocean/climate observing systems (GOOS/GCOS) for study of physical oceanography, the ocean carbon, oxygen and nutrient cycles, and marine biogeochemistry. GO-SHIP enables assessment of the ocean sequestration of heat and carbon, changing ocean circulation and ventilation patterns, and their effects on ocean health and Earth's climate. Rapid quality control and open data release along with incorporation of the GO-SHIP effort in the Joint Technical Commission for Oceanography and Marine Meteorology (JCOMM) in situ Observing Programs Support Center (JCOMMOPS) have increased the profile of, and participation in, the program and led to increased data use for a range of efforts. In addition to scientific discovery, GO-SHIP provides climate quality observations for ongoing calibration of measurements from existing and new autonomous platforms. This includes biogeochemical observations for the nascent array of biogeochemical (BGC)-Argo floats; temperature and salinity for Deep Argo; and salinity for the core Argo array. GO-SHIP provides the relevant suite of global, full depth, high quality observations and co-located deployment opportunities that, for the foreseeable future, remain crucial to maintenance and evolution of Argo's unique contribution to climate science. The evolution of GO-SHIP from a program primarily focused on physical climate to increased emphasis on ocean health and sustainability has put an emphasis on the addition of essential ocean variables for biology and ecosystems in the program measurement suite. In conjunction with novel automated measurement systems, ocean color, particulate matter, and phytoplankton enumeration are being explored as GO-SHIP variables. The addition of biological and ecosystem measurements will enable GO-SHIP to de

The wintertime spatial distribution of carbonate parameters in outer estuarine and coastal waters around Ireland is described from total alkalinity (TA) and dissolved inorganic carbon (DIC) data collected between 2010 and 2013. Due to predominantly limestone bedrock of their river catchments, the River Shannon and Barrow, Nore and Suir River system export high concentrations (>3800 μmol kg−1) of TA to their estuarine and inshore coastal waters where estuarine alkalinity decreases with increasing salinity. TA is lower in rivers with a non-calcareous bedrock, with positively correlated alkalinity-salinity relationships in both the Lee and Foyle outer estuaries. Winter pCO2 in the Shannon, Barrow/Nore/Suir and Lee estuaries is supersaturated relative to atmospheric CO2, while pCO2 in the outer Liffey estuary is slightly lower than atmospheric CO2 in three consecutive winters, indicative of a CO2 sink. Winter pCO2 is close to atmospheric equilibrium along the western shelf and through the centre of the Irish Sea, while it is a CO2 sink across the North Channel. While aragonite was supersaturated in most Irish waters, it was close to undersaturation in both the Lee estuary, attributed to its low alkalinity freshwater source, and Barrow/Nore/Suir estuary related to the flux of high concentrations of DIC from this river system. The seasonal impacts on inorganic carbon chemistry was also investigated by comparing winter and summer data collected between 2009 and 2013 along two transects in western coastal waters and along the western shelf edge. DIC was ~60 μmol kg−1 lower in summer relative to winter in the coastal transects and 39 μmol kg−1 lower along the shelf edge, accompanied by depleted nutrients and supersaturation of dissolved oxygen during summer, indicative of primary production. TA was generally higher in summer relative to winter corresponding with a decrease in nitrate, indicating that primary production dominated the TA distribution over calcification. An exc

The challenges of monitoring our waters for compliance with WFD and the expansion of the list of organic chemicals that are to be added for monitoring, provides impetus for investigation of alternative monitoring approaches such as passive sampling. The work being carried out represents an important collaboration between two research centres (DCU & MI) together with agency (EA UK and Inland Fisheries Ireland) and industry (TelLab) to assess the potential of passive sampling in monitoring priority pollutants in Ireland. The impact of this study may lie in the establishment of a capability to utilise passive sampling in the monitoring programme in Ireland for WFD. This project pilots the use of passive sampling technology (PDMS and POCIS) combined with biota monitoring to assess the presence of priority substances in Irish surface waters. The project focuses in particular on new pollutants earmarked as candidates for the Annex X priority substances list under the EU Water Framework Directive e.g. E2 and EE2, pharmaceuticals, pesticides, PFOS etc. This considers the implications for compliance with current and proposed EQS and investigates the potential for incorporating passive sampling and biota testing in future compliance, investigative and trend monitoring. . Results of water, biota and passive sampling will be presented together for samples collected in the Dublin catchment. A separate study on the occurrence of the pyrethroid pesticide cypermethrin was also conducted. Several sites along the River Liffey, Dublin, were sampled for pharmaceutical as well as other organic pollutants. A POCIS device was deployed at each location and water samples were collected at T-0 and T-4weeks. There are a number of potential point sources of pollution to this catchment with 3 wastewater treatment plants in the area. Pyrethroids have a low toxicity relative to other pesticides (specifically the organochlorines) so have recently been used in place of more toxic pesticides. Cyperm

The accumulation of anthropogenic CO2 in the oceans is altering seawater carbonate chemistry. Investigation and monitoring of the carbonate parameters is therefore necessary to understand potential impacts on ocean ecosystems. Total alkalinity (AT) and dissolved inorganic carbon (CT) were sampled across the Rockall Trough in Feb 2009 (CE0903) and Feb 2010 (CE10002) as part of a baseline study of inorganic carbon chemistry in Irish shelf waters. The results have been compared with data from WOCE surveys A01E (Sept 1991), A01 (Dec 1994), AR24 (Nov 1996) and A24 (June 1997). The 2009 and 2010 datasets provide a snapshot of the biogeochemical parameters which can act as a baseline of inorganic carbon and acidity levels in surface waters of the Rockall Trough in late winter for future comparison since previous surveys in the area have been affected by biological activity. The dataset also offers the possibility to compare decadal changes in subsurface waters. The temporal evolution of anthropogenic carbon (Delta C-ant) between the 1990s and 2010 was evaluated using two separate methods; (i) a comparison of the concentrations of C-T between surveys, after correcting it for remineralisation of organic material and formation and dissolution of calcium carbonate (Delta CT-abio) and (ii) an extended Multiple Linear Regression was used to calculate the Delta C-ant (Delta C-ant(eMLR)). There was an increase in Delta CT-abio and Delta C-ant(eMLR) of 18 +/- 4 mu mol kg(-1) and 19 +/- 4 mu mol kg(-1), respectively, in the subsurface waters between 1991 and 2010, equivalent to a decrease of 0.040 +/- 0.003 pH units over the 19 year period. There was an increase in both Delta CT-abio and Delta C(ant)e(mLR) of 8 +/- 4 mu mol kg(-1) in Labrador Sea Water (LSW) in the Trough between 1991 and 2010, and LSW has acidified by 0.029 +/- 0.002 pH units over the same time period. A reduction in calcite and aragonite saturation states was observed, which may have implications for calcifying or

The accumulation of anthropogenic CO2 in the oceans is altering seawater carbonate chemistry. Investigation and monitoring of the carbonate parameters is therefore necessary to understand potential impacts on ocean ecosystems. Total alkalinity (AT) and dissolved inorganic carbon (CT) were sampled across the Rockall Trough in Feb 2009 (CE0903) and Feb 2010 (CE10002) as part of a baseline study of inorganic carbon chemistry in Irish shelf waters. The results have been compared with data from WOCE surveys A01E (Sept 1991), A01 (Dec 1994), AR24 (Nov 1996) and A24 (June 1997). The 2009 and 2010 datasets provide a snapshot of the biogeochemical parameters which can act as a baseline of inorganic carbon and acidity levels in surface waters of the Rockall Trough in late winter for future comparison since previous surveys in the area have been affected by biological activity. The dataset also offers the possibility to compare decadal changes in subsurface waters. The temporal evolution of anthropogenic carbon (Delta C-ant) between the 1990s and 2010 was evaluated using two separate methods; (i) a comparison of the concentrations of C-T between surveys, after correcting it for remineralisation of organic material and formation and dissolution of calcium carbonate (Delta CT-abio) and (ii) an extended Multiple Linear Regression was used to calculate the Delta C-ant (Delta C-ant(eMLR)). There was an increase in Delta CT-abio and Delta C-ant(eMLR) of 18 +/- 4 mu mol kg(-1) and 19 +/- 4 mu mol kg(-1), respectively, in the subsurface waters between 1991 and 2010, equivalent to a decrease of 0.040 +/- 0.003 pH units over the 19 year period. There was an increase in both Delta CT-abio and Delta C(ant)e(mLR) of 8 +/- 4 mu mol kg(-1) in Labrador Sea Water (LSW) in the Trough between 1991 and 2010, and LSW has acidified by 0.029 +/- 0.002 pH units over the same time period. A reduction in calcite and aragonite saturation states was observed, which may have implications for calcifying or

The complex [Ru(bpy)2(CO)H]PF6 .l/2Acetone was synthesised in 50% yield. The reaction of this complex with a number of aldehydes, ketones and esters in buffered aqueous media and in an acidic acetonitrile environment revealed the reactivity to decrease in this order: Aldehydes > Ketones > Esters A kinetic study into the general acid catalysed reaction of this hydride complex with bgnzal^e^ydj was carried out and a rate coefficient of 1.3 10~ mol 1_| was calculated. An activation energy of 11.5 kJmol was calculated. High Performance Liquid Chromatography (H£LC) was used to demonstrate the conversion of [Ru(bpy)2 (CO)H] to [Ru(bpy)2 (CO)Cl] in acetonitrile by addition of HC1. Reverse phase ion pair chromatography (RP.IPC) and cation exchange chromatography were used for the analysis of ruthenium bis (2,21-bipyridyl), (bpy), complexes using a range of mobile phases with lithium perchlorate, (LiClO^), as an additive. A C18 and a CN column were not suitable for the analysis due to peak distortion problems. A cation exchange, (CX), column provided a useful method for the separation of these compounds. Plots of %acetonitrile, (MeCN), vs. retention time at given LiCl04 concentration suggested a change in the dominant retention mechanism, possibly from cation exchange to RP.IPC with increaing water content in the mobile phase. The presence of split peaks for the dicationic complexes at 80%MeCN : 20%H20 ; 0.1M LiC104 as mobile phase was attributed to competing retention mechanisms. The optimum system for the separation of the compounds examined was 80%MeCN : 20%H„0 ; 0.08M LiC104 at a flow rate of 2.5ml/min. The Photolyses of [Ru(bpy)2L2]2+ [Ru(bpy)2 (L)C1]+ , (L = imidazole / vinylimidazole), in MeCN was studied on an ODS and a CX column using the system developed. The ligand was replaced in these reactions to give [Ru(bpy)2(MeCN)2 ] + for the dicationic compounds and [Ru(bpy)2 (MeCN)Cl] for the monocationic compounds as the major final products. Other unidentified products