The inhibition of marine nitrification by ocean disposal of carbon dioxide

In an attempt to reduce the threat of global warming, it has been proposed that the rise of atmospheric carbon dioxide concentrations be reduced by the ocean disposal of CO2 from the flue gases of fossil fuel-fired power plants. The release of large amounts of CO2 into mid or deep ocean waters will result in large plumes of acidified seawater with pH values ranging from 6 to 8. In an effort to determine whether these CO2-induced pH changes have any effect on marine nitrification processes, surficial (euphotic zone) and deep (aphotic zone) seawater samples were sparged with CO2 for varying time durations to achieve a specified pH reduction, and the rate of microbial ammonia oxidation was measured spectrophotometrically as a function of pH using an inhibitor technique. For both seawater samples taken from either the euphotic or aphotic zone, the nitrification rates dropped drastically with decreasing pH. Relative to nitrification rates in the original seawater at pH 8, nitrification rates were reduced by ca. 50% at pH 7 and more than 90% at pH 6.5. Nitrification was essentially completely inhibited at pH 6. These findings suggest that the disposal of CO2 into mid or deep oceans will most likely result in a drastic reduction of ammonia oxidation rates within the pH plume and the concomitant accumulation of ammonia instead of nitrate. It is unlikely that ammonia will reach the high concentration levels at which marine aquatic organisms are known to be negatively affected. However, if the ammonia-rich seawater from inside the pH plume is upwelled into the euphotic zone, it is likely that changes in phytoplankton abundance and community structure will occur. Finally, the large-scale inhibition of nitrification and the subsequent reduction of nitrite and nitrate concentrations could also result in a decrease of denitrification rates which, in turn, could lead to the buildup of nitrogen and unpredictable eutrophication phenomena. Clearly, more research on the environmental effects of ocean disposal of CO2 is needed to determine whether the potential costs related to marine ecosystem disturbance and disruption can be justified in terms of the perceived benefits that may be achieved by temporarily delaying global warming.     

Comparison of the acid-base responses to CO2 and acidification in Japanese flounder (Paralichthys olivaceus)

To investigate whether the biological toxicity of aquatic hypercapnia is due to the direct effects of CO2 or to the effects of acidification of seawater by CO2, the Japanese flounder (Paralichthys olivaceus) was subjected to seawater equilibrated with a gas mixture of air containing 5% CO2 (pH 6.18) or seawater acidified to the same pH with 1 N H2SO4. All the fish died within 72 h in the CO2 exposure group, whereas no mortality occurred in the acid group. Acid-base parameters as well as plasma ion concentrations were severely perturbed in the CO2 exposure group, whereas they were minimally affected in the acid group. These results clearly demonstrate that the mortality in the CO2 group is a direct result of the elevated levels of dissolved CO2 and not to the effects of the reduced water pH.     

Comparison of the lethal effect of CO2 and acidification on red sea bream (Pagrus major) during the early developmental stages

To compare the acute toxicity of CO(2)- and HCl-acidified seawater, eggs and larvae of a marine fish, Pagrus major, were exposed to seawater equilibrated with CO(2)-enriched gas mixtures (CO(2)=5% or 10%, O(2)=20.95% balanced with N(2)) or seawater acidified with 1 N HCl at two pH levels (pH 6.2 (=5% CO(2)) and 5.9 (=10% CO(2))) for 6 h (eggs) or 24 h (larvae). Mortalities of eggs were 85.8% (CO(2)) and 3.6% (HCl) at pH 6.2, and 97.4% (CO(2)) and 0.9% (HCl) at pH 5.9, while those of larvae were 61.2% (CO(2)) and 1.6% (HCl) at pH 6.2, and 100% (CO(2)) and 5.0% (HCl) at pH 5.9. Thus, previous research on the effects of acidified seawater on marine organisms, as a substitute for CO(2), has largely underestimated the toxic effects of CO(2).     

The extent of hydrocarbon contamination in the marine environment from a research station in the Antarctic

Low level hydrocarbon contamination is measurable in the vicinity of Antarctic stations, N-alkane and polycyclic aromatic hydrocarbon (PAH) concentrations in seawater and sediment at Signy Station, South Orkney Islands indicated contamination was confined to within a few hundred metres of the station. Total n-alkane concentrations in seawater decreased from 7.6 to 2.6 μg l⁻¹ within 500 m of the station. All n-alkane values in seawater were within the limits of variation for oceanic waters proposed by cripps (1992), although the distribution pattern suggested pollution from the station. The total PAH concentration in seawater varied between 110 and 216 ng l⁻¹. These values showed no trend with distance from the station and were all slightly higher than for the open ocean. The n-alkane and PAH concentations in the surface sediment declined to low levels within 375 m of the station. This indicates that a large proportion of the hydrocarbons entering Factory Cove was deposited from the water column. Sediment n-alkane concentrations were similar at all depths of the cores when collected more than 125 m from the station. PAH levels in the sediment appeared to be due to local input, including a small spill in 1965.     

Effects of raised CO2 concentration on the egg production rate and early development of two marine copepods (Acartia steueri and Acartia erythraea)

Direct injection of CO(2) into the deep ocean is receiving increasing attention as a way to mitigate increasing atmospheric CO(2) concentration. To assess the potential impact of the environmental change associated with CO(2) sequestration in the ocean, we studied the lethal and sub-lethal effects of raised CO(2) concentration in seawater on adult and early stage embryos of marine planktonic copepods. We found that the reproduction rate and larval development of copepods are very sensitive to increased CO(2) concentration. The hatching rate tended to decrease, and nauplius mortality rate to increase, with increased CO(2) concentration. These results suggest that the marine copepod community will be negatively affected by the disposal of CO(2). This could decrease on the carbon export flux to the deep ocean and change the biological pump. Clearly, further studies are needed to determine whether ocean CO(2) injection is an acceptable strategy to reduce anthropogenic CO(2).     

Geochemical survey of Levante Bay,Vulcano Island (Italy), a natural laboratory for the study of ocean acidification

Shallow submarine gas vents in Levante Bay, Vulcano Island (Italy), emit around 3.6t CO₂ per day providing a natural laboratory for the study of biogeochemical processes related to seabed CO₂ leaks and ocean acidification. The main physico-chemical parameters (T, pH and Eh) were measured at more than 70 stations with 40 seawater samples were collected for chemical analyses. The main gas vent area had high concentrations of dissolved hydrothermal gases, low pH and negative redox values all of which returned to normal seawater values at distances of about 400 m from the main vents. Much of the bay around the vents is corrosive to calcium carbonate; the north shore has a gradient in seawater carbonate chemistry that is well suited to studies of the effects of long-term increases in CO₂ levels. This shoreline lacks toxic compounds (such as H₂S) and has a gradient in carbonate saturation states.     

Effects of high CO2 seawater on the copepod (Acartia tsuensis) through all life stages and subsequent generations

We studied the effects of exposure to seawater equilibrated with CO(2)-enriched air (CO(2) 2380 ppm) from eggs to maturity and over two subsequent generations on the copepod Acartia tsuensis. Compared to the control (CO(2) 380 ppm), high CO(2) exposure through all life stages of the 1st generation copepods did not significantly affect survival, body size or developmental speed. Egg production and hatching rates were also not significantly different between the initial generation of females exposed to high CO(2) and the 1st and 2nd generation females developed from eggs to maturity in high CO(2). Thus, the copepods appear more tolerant to increased CO(2) than other marine organisms previously investigated for CO(2) tolerance (i.e., sea urchins and bivalves). However, the crucial importance of copepods in marine ecosystems requires thorough evaluation of the overall impacts of marine environmental changes predicted to occur with increased CO(2) concentrations, i.e., increased temperature, enhanced UV irradiation, and changes in the community structure and nutritional value of phytoplankton.     

A marine secondary producer respires and feeds more in a high CO2 ocean

Climate change mediates marine chemical and physical environments and therefore influences marine organisms. While increasing atmospheric CO(2) level and associated ocean acidification has been predicted to stimulate marine primary productivity and may affect community structure, the processes that impact food chain and biological CO(2) pump are less documented. We hypothesized that copepods, as the secondary marine producer, may respond to future changes in seawater carbonate chemistry associated with ocean acidification due to increasing atmospheric CO(2) concentration. Here, we show that the copepod, Centropages tenuiremis, was able to perceive the chemical changes in seawater induced under elevated CO(2) concentration (>1700 μatm, pH<7.60) with avoidance strategy. The copepod's respiration increased at the elevated CO(2) (1000 μatm), associated acidity (pH 7.83) and its feeding rates also increased correspondingly, except for the initial acclimating period, when it fed less. Our results imply that marine secondary producers increase their respiration and feeding rate in response to ocean acidification to balance the energy cost against increased acidity and CO(2) concentration.     

Organochlorine compound and trace metal contaminants in fish near Sydney's ocean outfalls

Sydney's inshore sewage outfalls were significant contributors to organochlorine contamination of inshore sedentary fish such as red morwong. Diversion of the sewage to deepwater outfalls has resulted in marked declines in the concentrations of these compounds in inshore red morwong. Apart from lead, however, similar trends did not occur for concentrations of trace metals. A wide variety of trace metals and organochlorine compounds were found in the flesh and/or livers of a variety of fish species caught at sites associated with the present deepwater ocean outfalls off Sydney. Fish caught at locations remote from Sydney also contained a wide variety of trace metals although organochlorine compounds were usually at lower levels. The mean contaminant levels in all species of offshore fish were generally found to be low when compared to the Australian National Food Authority's Maximum Residue Limit (NFA MRL). No fish analysed was found to have levels of an organochlorine compound above the MRL and no fish was found to have levels of zinc or lead above the MRL. When detected, fish with levels of a trace metal above the MRL appeared to be distributed throughout New South Wales, independent of the deepwater ocean outfalls off Sydney. There is no evidence as yet that the commissioning of the deepwater outfalls has led to an increase in levels of contaminants in the fish examined to the extent that they are of concern relative to the NFA MRLs.     

Community-level response of coastal microbial biofilms to ocean acidification in a natural carbon dioxide vent ecosystem

The impacts of ocean acidification on coastal biofilms are poorly understood. Carbon dioxide vent areas provide an opportunity to make predictions about the impacts of ocean acidification. We compared biofilms that colonised glass slides in areas exposed to ambient and elevated levels of pCO(2) along a coastal pH gradient, with biofilms grown at ambient and reduced light levels. Biofilm production was highest under ambient light levels, but under both light regimes biofilm production was enhanced in seawater with high pCO(2). Uronic acids are a component of biofilms and increased significantly with high pCO(2). Bacteria and Eukarya denaturing gradient gel electrophoresis profile analysis showed clear differences in the structures of ambient and reduced light biofilm communities, and biofilms grown at high pCO(2) compared with ambient conditions. This study characterises biofilm response to natural seabed CO(2) seeps and provides a baseline understanding of how coastal ecosystems may respond to increased pCO(2) levels.     

Human impacts on large benthic foraminifers near a densely populated area of Majuro Atoll, Marshall Islands

Human impacts on sand-producing, large benthic foraminifers were investigated on ocean reef flats at the northeast Majuro Atoll, Marshall Islands, along a human population gradient. The densities of dominant foraminifers Calcarina and Amphistegina declined with distance from densely populated islands. Macrophyte composition on ocean reef flats differed between locations near sparsely or densely populated islands. Nutrient concentrations in reef-flat seawater and groundwater were high near or on densely populated islands. δ¹⁵N values in macroalgal tissues indicated that macroalgae in nearshore lagoons assimilate wastewater-derived nitrogen, whereas those on nearshore ocean reef flats assimilate nitrogen from other sources. These results suggest that increases in the human population result in high nutrient loading in groundwater and possibly into nearshore waters. High nutrient inputs into ambient seawater may have both direct and indirect negative effects on sand-producing foraminifers through habitat changes and/or the collapse of algal symbiosis.     

Potential acidification impacts on zooplankton in CCS leakage scenarios

Carbon capture and storage (CCS) technologies involve localized acidification of significant volumes of seawater, inhabited mainly by planktonic species. Knowledge on potential impacts of these techniques on the survival and physiology of zooplankton, and subsequent consequences for ecosystem health in targeted areas, is scarce. The recent literature has a focus on anthropogenic greenhouse gas emissions into the atmosphere, leading to enhanced absorption of CO₂ by the oceans and a lowered seawater pH, termed ocean acidification. These studies explore the effects of changes in seawater chemistry, as predicted by climate models for the end of this century, on marine biota. Early studies have used unrealistically severe CO₂/pH values in this context, but are relevant for CCS leakage scenarios. Little studied meso- and bathypelagic species of the deep sea may be especially vulnerable, as well as vertically migrating zooplankton, which require significant residence times at great depths as part of their life cycle.     

Occurrence and concentration of caffeine in Oregon coastal waters

Caffeine, a biologically active drug, is recognized as a contaminant of freshwater and marine systems. We quantified caffeine concentrations in Oregon's coastal ocean to determine whether levels correlated with proximity to caffeine pollution sources. Caffeine was analyzed at 14 coastal locations, stratified between populated areas with sources of caffeine pollution and sparsely populated areas with no major caffeine pollution sources. Caffeine concentrations were measured in major water bodies discharging near sampling locations. Caffeine in seawater ranged from below the reporting limit (8.5 ng/L) to 44.7 ng/L. Caffeine occurrence and concentrations in seawater did not correspond with pollution threats from population density and point and non-point sources, but did correspond with storm event occurrence. Caffeine concentrations in rivers and estuaries draining to the coast ranged from below the reporting limit to 152.2 ng/L. This study establishes the occurrence of caffeine in Oregon's coastal waters, yet relative importance of sources, seasonal variability, and processes affecting caffeine transport into the coastal ocean require further research.     

Incorporation of organic tritium (3H) by marine organisms and sediment in the severn estuary/Bristol channel (UK).

Discharges of tritium (3H) into the Severn estuary/Bristol Channel (UK) arise from the authorized release of wastes from nuclear power plants at Hinkley Point and Berkley/Oldbury and from the Nycomed-Amersham radiochemical plant, via the sewer system, at Cardiff. The wastes from the nuclear power plants probably consist almost entirely of 3H2O, whereas those from the radiochemical plant also include uncharacterized 3H labelled organic compounds. The total 3H concentrations in demersal fish and other benthic organisms in the vicinity of the Cardiff Eastern sewer outfall are significantly elevated compared to those observed around other UK nuclear establishments. Concentrations in filtered seawater were approximately 10 Bq kg(-1) whilst levels in surface sediment, seaweed (Fucus vesiculosis) and mussels (Mytilus edulis)/flounder (Platichthys flesus) were in the order of 6 x 10(2), 2 x 10(3), and 10(5) Bq kg(-1) (dry weight), respectively. Almost all the 3H found in sediment and biota were organically bound tritium (OBT). The high concentration in these materials, relative to that in seawater, is due to the presence of bioavailable organic 3H labelled compounds in the radiochemical waste. It is suggested that bioaccumulation of 3H by benthic organisms and demersal fish occurs primarily via a pathway of physico-chemical sorption/bacterial transformation of dissolved 3H labelled organic compounds into particulate organic matter, and subsequent transfer up a web of sediment dwelling microbes and meiofauna. Variations in 3H accumulation between individual organisms have been interpreted in terms of their different feeding behaviour. Relatively low concentrations were observed in the herbivorous winkle (Littorina littorea) and the pelagic Sprat (Spratus spratus) compared with other benthic organisms and demersal fish. The elevated 3H concentrations in seafood, due to bioaccumulation of OBT, have low radiological significance even for the local critical group of seafood consumers.     

A review of pollutants in the sea-surface microlayer (SML): a unique habitat for marine organisms

Boundary layers between different environmental compartments represent critical interfaces for biological, chemical and physical processes. The sea-surface microlayer (uppermost 1-1000 microm layer) forms the boundary layer interface between the atmosphere and ocean. Environmental processes are controlled by the SML, and it is known to play a key role in the global distribution of anthropogenic pollutants. Due to its unique chemical composition, the upper organic film of the SML represents both a sink and a source for a range of pollutants including chlorinated hydrocarbons, organotin compounds, petroleum hydrocarbons, polycyclic aromatic hydrocarbons (PAH) and heavy metals. These pollutants can be enriched in the SML by up to 500 times relative to concentrations occurring in the underlying bulk water column. The SML is also a unique ecosystem, serving as an important habitat for fish eggs and larvae. Concentration ranges and enrichment factors of pollutants in the SML in different areas of the world's oceans have been critically reviewed, together with available toxicity data for marine biota found within the SML. Overall, the SML is highly contaminated in many urban and industrialized areas of the world, resulting in severe ecotoxicological impacts. Such impacts may lead to drastic effects on the marine food web and to fishery recruitment in coastal waters. Studies of the toxicity of fish eggs and larvae exposed to the SML contaminants have shown that the SML in polluted areas leads to significantly higher rates of mortality and abnormality of fish embryos and larvae.     

On the accuracy of the bathymetry-generated gravitational field quantities for a depth-dependent seawater density distribution

In geophysical studies investigating the lithosphere structure, the gravitational field generated by the ocean density contrast (i.e., bathymetry-generated gravitational field) represents a significant amount of the signal to be modelled and subsequently removed from the Earth’s gravity field. The ocean density contrast is typically calculated as the difference between the mean density values of the Earth’s crust and seawater. The approximation of the actual seawater density distribution by its mean value yields relative errors up to about 2% in computed quantities of the gravitational field. To reduce these errors, a more realistic model of the seawater density distribution is utilized based on the analysis of existing oceanographic data of salinity, temperature, and pressure (depth). We study the accuracy of the bathymetry-generated gravitational field quantities formulated for a depth-dependent model of the seawater density distribution. This density distribution approximates the seawater density variations due to an increasing pressure with depth, whereas smaller lateral density variations caused by salinity, temperature, and other oceanographic factors are not taken into consideration. The error analysis reveals that the approximation of the seawater density by the depth-dependent density model reduces the maximum errors to less than 0.6%. The corresponding depth-averaged errors are below 0.1%. The depth-dependent seawater density model is further facilitated in expressions for computing the bathymetry-generated gravitational field quantities by means of the spherical bathymetric (ocean bottom depth) functions. The numerical realization reveals large differences in the results obtained with and without consideration of the depth-dependent seawater density distribution. The maxima of absolute differences reach 201 m²/s² and 16.5 mGal in computed values of the potential and attraction, respectively. The application of the depth-dependent seawater density model thus significantly improves the accuracy in the forward modelling of the bathymetric gravitational field quantities.     

Sewage impacts coral reefs at multiple levels of ecological organization

Against a backdrop of rising sea temperatures and ocean acidification which pose global threats to coral reefs, excess nutrients and turbidity continue to be significant stressors at regional and local scales. Because interventions usually require local data on pollution impacts, we measured ecological responses to sewage discharges in Surin Marine Park, Thailand. Wastewater disposal significantly increased inorganic nutrients and turbidity levels, and this degradation in water quality resulted in substantial ecological shifts in the form of (i) increased macroalgal density and species richness, (ii) lower cover of hard corals, and (iii) significant declines in fish abundance. Thus, the effects of nutrient pollution and turbidity can cascade across several levels of ecological organization to change key properties of the benthos and fish on coral reefs. Maintenance or restoration of ecological reef health requires improved wastewater management and run-off control for reefs to deliver their valuable ecosystems services.     

239+240Pu and 137Cs concentrations for zooplankton and nekton in the Northwest Pacific and Antarctic Oceans (1993-1996)

The concentrations of 239+240Pu and 137Cs in zooplankton and nekton in the Northwest Pacific and Southern Oceans were measured during the period 1993-1996. The object of the sampling was to assess the potential impacts of existing submerged anthropogenic-radioactive materials in the western North Pacific as well as the East China Sea. Samples from the Bransfield Strait of the Antarctic Ocean provided a control source impacted by only atmospheric bomb fallout. No particularly elevated levels of 239+240Pu were found in zooplankton samples from the Northwest Pacific, although significantly lower levels of 239+240Pu were found in three mixed zooplankton samples from the Bransfield Strait. The body burden of 239+240Pu in zooplankton appears to reflect concentrations in ambient seawater with some variation. Some additional measurements of 137Cs in fish are also reported here to complement existing databases and for future reference in the regional marine environmental radioactivity monitoring effort.     

Mediating stream baseflow response to climate change: The role of basin storage

Inter‐basin differences in streamflow response to changes in regional hydroclimatology may reflect variations in storage characteristics that control the retention and release of water inputs. These aspects of storage could mediate a basin's sensitivity to climate change. The hypothesis that temporal trends in stream baseflow exhibit a more muted reaction to changes in precipitation and evapotranspiration for basins with greater storage was tested on the Oak Ridges Moraine (ORM) in Southern Ontario, Canada. Long‐term (>25 years) baseflow trends for 16 basins were compared to corresponding trends in precipitation amount and type and in potential evapotranspiration as well as shorter trends in groundwater levels for monitoring wells on the ORM. Inter‐basin differences in storage properties were characterized using physiographic, hydrogeologic, land use/land cover, and streamflow metrics. The latter included the slope of the basin's flow duration curve and basin dynamic storage. Most basins showed temporal increases in baseflow, consistent with limited evidence of increases and decreases in regional precipitation and snowfall: precipitation ratio, respectively, and recent increases in groundwater recharge along the crest of the ORM. Baseflow trend magnitude was uncorrelated to basin physiographic, hydrogeologic, land use/land cover, or flow duration curve characteristics. However, it was positively related to a basin's dynamic storage, particularly for basins with limited coverage of open water and wetlands. The dynamic storage approach assumes that a basin behaves as a first‐order dynamical system, and extensive open water and wetland areas in a basin may invalidate this assumption. Previous work suggested that smaller dynamic storage was linked to greater damping of temporal variations in water inputs and reduced interannual variability in streamflow regime. Storage and release of water inputs to a basin may assist in mediating baseflow response to temporal changes in regional hydroclimatology and may partly account for inter‐basin differences in that response. Such storage characteristics should be considered when forecasting the impacts of climate change on regional streamflow.     

Banking carbon: a review of organic carbon storage and physical factors influencing retention in floodplains and riparian ecosystems

Rivers are dynamic components of the terrestrial carbon cycle and provide important functions in ecosystem processes. Although rivers act as conveyers of carbon to the oceans, rivers also retain carbon within riparian ecosystems along floodplains, with potential for long‐term (> 10² years) storage. Research in ecosystem processing emphasizes the importance of organic carbon (OC) in river systems, and estimates of OC fluxes in terrestrial freshwater systems indicate that a significant portion of terrestrial carbon is stored within river networks. Studies have examined soil OC on floodplains, but research that examines the potential mechanistic controls on OC storage in riparian ecosystems and floodplains is more limited. We emphasize three primary OC reservoirs within fluvial systems: (1) standing riparian biomass; (2) dead biomass as large wood (LW) in the stream and on the floodplain; (3) OC on and beneath the floodplain surface, including litter, humus, and soil organic carbon (SOC). This review focuses on studies that have framed research questions and results in the context of OC retention, accumulation and storage within the three primary pools along riparian ecosystems. In this paper, we (i) discuss the various reservoirs for OC storage in riparian ecosystems, (ii) discuss physical conditions that facilitate carbon retention and storage in riparian ecosystems, (iii) provide a synthesis of published OC storage in riparian ecosystems, (iv) present a conceptual model of the conditions that favor OC storage in riparian ecosystems, (v) briefly discuss human impacts on OC storage in riparian ecosystems, and (vi) highlight current knowledge gaps. Copyright © 2015 John Wiley & Sons, Ltd.