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We investigated whether CO2-induced ocean acidification (OA) affects dopamine receptor-dependent behavior in bicolor damselfish (Stegastes partitus). Damselfish were kept in aquaria receiving flow through control (pH ~ 8.03; pCO2 ~ 384 μatm) or OA (pH ~ 7.64; CO2 ~ 1100 μatm) seawater at a rate of 1 L min-1. Despite this relatively fast flow rate, fish respiration further acidified the seawater in both control (pH ~7.88; pCO2 ~ 595 μatm) and OA (pH ~7.55; pCO2 ~ 1450 μatm) fish-holding aquaria. After five days of exposure, damselfish locomotion, boldness, anxiety, and aggression were assessed using a battery of behavioral tests using automated video analysis. Two days later, these tests were repeated following application of the dopamine D1 receptor agonist SKF 38393. OA-exposure induced ceiling anxiety levels that were significantly higher than in control damselfish, and SKF 38393 increased anxiety in control damselfish to a level not significantly different than that of OA-exposed damselfish. Additionally, SKF 38393 decreased locomotion and increased boldness in control damselfish but had no effect in OA-exposed damselfish, suggesting an alteration in activity of dopaminergic pathways that regulate behavior under OA conditions. These results indicate that changes in dopamine D1 receptor function affects fish behavior during exposure to OA. However, subsequent measurements of seawater sampled using syringes during the daytime (~3-4 pm local time) from crevasses in coral reef colonies, which are used as shelter by damselfish, revealed an average pH of 7.73 ± 0.03 and pCO2 of 925.8 ± 62.2 μatm; levels which are comparable to Representative Concentration Pathway (RCP) 8.5 predicted end-of-century mean OA levels in the open ocean. Further studies considering the immediate environmental conditions experienced by fish as well as individual variability and effect size are required to understand potential implications of the observed OA-induced behavioral effects on damselfish fitness in the wild.

The oceans play a key role in climate regulation especially in part buffering (neutralising) the effects of increasing levels of greenhouse gases in the atmosphere and rising global temperatures. This chapter examines how the regulatory processes performed by the oceans alter as a response to climate change and assesses the extent to which positive feedbacks from the ocean may exacerbate climate change. There is clear evidence for rapid change in the oceans. As the main heat store for the world there has been an accelerating change in sea temperatures over the last few decades, which has contributed to rising sea-level. The oceans are also the main store of carbon dioxide (CO2), and are estimated to have taken up approximately 40% of anthropogenic-sourced CO2 from the atmosphere since the beginning of the industrial revolution. A proportion of the carbon uptake is exported via the four ocean 'carbon pumps' (Solubility, Biological, Continental Shelf and Carbonate Counter) to the deep ocean reservoir. Increases in sea temperature and changing planktonic systems and ocean currents may lead to a reduction in the uptake of CO2 by the ocean; some evidence suggests a suppression of parts of the marine carbon sink is already underway. While the oceans have buffered climate change through the uptake of CO2 produced by fossil fuel burning this has already had an impact on ocean chemistry through ocean acidification and will continue to do so. Feedbacks to climate change from acidification may result from expected impacts on marine organisms (especially corals and calcareous plankton), ecosystems and biogeochemical cycles. The polar regions of the world are showing the most rapid responses to climate change. As a result of a strong ice-ocean influence, small changes in temperature, salinity and ice cover may trigger large and sudden changes in regional climate with potential downstream feedbacks to the climate of the rest of the world. A warming Arctic Ocean may lead to further releases of the potent greenhouse gas methane from hydrates and permafrost. The Southern Ocean plays a critical role in driving, modifying and regulating global climate change via the carbon cycle and through its impact on adjacent Antarctica. The Antarctic Peninsula has shown some of the most rapid rises in atmospheric and oceanic temperature in the world, with an associated retreat of the majority of glaciers. Parts of the West Antarctic ice sheet are deflating rapidly, very likely due to a change in the flux of oceanic heat to the undersides of the floating ice shelves. The final section on modelling feedbacks from the ocean to climate change identifies limitations and priorities for model development and associated observations. Considering the importance of the oceans to climate change and our limited understanding of climate-related ocean processes, our ability to measure the changes that are taking place are conspicuously inadequate. The chapter highlights the need for a comprehensive, adequately funded and globally extensive ocean observing system to be implemented and sustained as a high priority. Unless feedbacks from the oceans to climate change are adequately included in climate change models, it is possible that the mitigation actions needed to stabilise CO2 and limit temperature rise over the next century will be underestimated.

Abstract: The uptake of atmospheric carbon dioxide (CO2) into the mid-latitudes of the North Atlantic Ocean through the production of wintertime Sub-Tropical Mode Water (STMW) also known as Eighteen Degree Water (EDW) is poorly quantified and constrained. Nonetheless, it has been proposed that the EDW could serve as an important short-term sink of anthropogenic CO2. The objective of the present investigation was to determine sea–air CO2 gas exchange rates and seawater CO2 dynamics during wintertime formation of EDW in the North Atlantic Ocean. During 2006 and 2007, several research cruises were undertaken as part of the CLIMODE project across the northwest Atlantic Ocean with the intent to study the pre-conditioning, formation, and the evolution of EDW. Sea–air CO2 exchange rates were calculated based on measurements of atmospheric pCO2, surface seawater pCO2 and wind speed with positive values denoting a net flux from the surface ocean to the atmosphere. Average sea–air CO2 flux calculated along cruise tracks in the formation region equaled −18±6mmol CO2 m−2 d−1 and −14±9mmol CO2 m−2 d−1 in January of 2006 and March of 2007, respectively. Average sea–air CO2 flux in newly formed outcropping EDW in February and March of 2007 equaled −28±10mmol CO2 m−2 d−1. These estimates exceeded previous flux estimates in this region by 40–185%. The magnitude of CO2 flux was mainly controlled by the observed variability in wind speed and ΔpCO2 with smaller changes owing to variability in sea surface temperature. Small but statistically significant difference (4.1±2.6μmolkg−1) in dissolved inorganic carbon (DIC) was observed in two occurrences of newly formed EDW in February and March of 2007. This difference was explained either by differences in the relative contribution from different water masses involved in the initial formation process of EDW or temporal changes owing to sea–air CO2 exchange (∼25%) and vertical and/or lateral mixing (∼75%) with water masses high in DIC from the cold side of the Gulf Stream and/or from below the permanent thermocline. Based on the present estimate of sea–air CO2 flux in newly formed EDW and a formation rate of 9.3Svy (Sverdrup year=106 m3 s−1 flow sustained for 1 year), CO2 uptake by newly formed EDW may constitute 3–6% of the total North Atlantic CO2 sink. However, advection of surface waters that carry an elevated burden of anthropogenic CO2 that are transported to the formation region and transformed to mode water may contribute additional CO2 to the total net uptake and sequestration of anthropogenic CO2 to the ocean interior. [Copyright &y& Elsevier]

Ocean acidification produced by dissolution of anthropogenic carbon dioxide (CO2) emissions in seawater has profound consequences for marine ecology and biogeochemistry. The oceans have absorbed one-third of CO2 emissions over the past two centuries, altering ocean chemistry, reducing seawater pH, and affecting marine animals and phytoplankton in multiple ways. Microbially mediated ocean biogeochemical processes will be pivotal in determining how the earth system responds to global environmental change; however, how they may be altered by ocean acidification is largely unknown. We show here that microbial nitrification rates decreased in every instance when pH was experimentally reduced (by 0.05-0.14) at multiple locations in the Atlantic and Pacific Oceans. Nitrification is a central process in the nitrogen cycle that produces both the greenhouse gas nitrous oxide and oxidized forms of nitrogen used by phytoplankton and other microorganisms in the sea; at the Bermuda Atlantic Time Series and Hawaii Ocean Time-series sites, experimental acidification decreased ammonia oxidation rates by 38% and 36%. Ammonia oxidation rates were also strongly and inversely correlated with pH along a gradient produced in the oligotrophic Sargasso Sea (r² = 0.87, P < 0.05). Across all experiments, rates declined by 8-38% in low pH treatments, and the greatest absolute decrease occurred where rates were highest off the California coast. Collectively our results suggest that ocean acidification could reduce nitrification rates by 3-44% within the next few decades, affecting oceanic nitrous oxide production, reducing supplies of oxidized nitrogen in the upper layers of the ocean, and fundamentally altering nitrogen cycling in the sea. [ABSTRACT FROM AUTHOR]

The shallow-water ocean environment is of great importance in the context of global change and is heavily impacted by human activity. This study evaluates the effects of human activity on the CO2 exchange between the atmosphere and the surface water of shallow-water oceans. The evaluation is based on changes in net ecosystem metabolism, net ecosystem calcification, and atmospheric CO2 concentrations, as seen in a process-driven biogeochemical box model. Numerical simulations show that this air-sea interface has probably served as a net source of CO2 to the atmosphere for much of the past 300 years, but has recently switched, or will switch soon, to a net sink of CO2, because of rising atmospheric CO2 and increasing inorganic nutrient load. [ABSTRACT FROM AUTHOR]

The shallow-water ocean environment is of great importance in the context of global change and is heavily impacted by human activity. This study evaluates the effects of human activity on the CO2 exchange between the atmosphere and the surface water of shallow-water oceans. The evaluation is based on changes in net ecosystem metabolism, net ecosystem calcification, and atmospheric CO2 concentrations, as seen in a process-driven biogeochemical box model. Numerical simulations show that this air-sea interface has probably served as a net source of CO2 to the atmosphere for much of the past 300 years, but has recently switched, or will switch soon, to a net sink of CO2, because of rising atmospheric CO2 and increasing inorganic nutrient load. [ABSTRACT FROM AUTHOR]

Abstract: Epochs of changing atmospheric CO2 and seawater CO2–carbonic acid system chemistry and acidification have occurred during the Phanerozoic at various time scales. On the longer geologic time scale, as sea level rose and fell and continental free board decreased and increased, respectively, the riverine fluxes of Ca, Mg, DIC, and total alkalinity to the coastal ocean varied and helped regulate the C chemistry of seawater, but nevertheless there were major epochs of ocean acidification (OA). On the shorter glacial–interglacial time scale from the Last Glacial Maximum (LGM) to late preindustrial time, riverine fluxes of DIC, total alkalinity, and N and P nutrients increased and along with rising sea level, atmospheric PCO2 and temperature led, among other changes, to a slightly deceasing pH of coastal and open ocean waters, and to increasing net ecosystem calcification and decreasing net heterotrophy in coastal ocean waters. From late preindustrial time to the present and projected into the 21st century, human activities, such as fossil fuel and land-use emissions of CO2 to the atmosphere, increasing application of N and P nutrient subsidies and combustion N to the landscape, and sewage discharges of C, N, P have led, and will continue to lead, to significant modifications of coastal ocean waters. The changes include a rapid decline in pH and carbonate saturation state (modern problem of ocean acidification), a shift toward dissolution of carbonate substrates exceeding production, potentially leading to the “demise” of the coral reefs, reversal of the direction of the sea-to-air flux of CO2 and enhanced biological production and burial of organic C, a small sink of anthropogenic CO2, accompanied by a continuous trend toward increasing autotrophy in coastal waters. [Copyright &y& Elsevier]