Ocean acidification (OA) is likely to have an effect on the fertilizing potential of desert dust in high-nutrient, low-chlorophyll oceanic regions, either by modifying iron (Fe) speciation and bioavailability or by altering phytoplankton Fe requirements and acquisition. To address this issue, short incubations (4 days) of northeast subarctic Pacific waters enriched with either FeSO4 or dust and set at pH 8.0 (in situ) and 7.8 were conducted in August 2010.
Increasing atmospheric CO2 concentrations are causing decreased pH over vast expanses of the ocean. This decreasing pH may alter biogeochemical cycling of carbon and nitrogen via the microbial process of nitrification, a key process that couples these cycles in the ocean, but which is often sensitive to acidic conditions. Recent reports have indicated a decrease in oceanic nitrification rates under experimentally lowered pH. How the composition and abundance of ammonia-oxidizing bacteria (AOB) and archaea (AOA) assemblages respond to decreasing oceanic pH is unknown.
In an ocean with rapidly changing chemistry, studies have assessed coral skeletal health under projected ocean acidification (OA) scenarios by characterizing morphological distortions in skeletal architecture and measuring bulk properties, such as net calcification and dissolution. Few studies offer more detailed information on skeletal mineralogy. Since aragonite crystallography will at least partially govern the material properties of coral skeletons, such as solubility and strength, it is important to understand how it is influenced by environmental stressors.
Kelp forests are among the world's most productive marine ecosystems, yet little is known about their biogeochemistry. This study presents a 14-month time series (July 2013–August 2014) of surface and benthic dissolved inorganic carbon and total alkalinity measurements, along with accompanying hydrographic measurements, from six locations within a central California kelp forest. We present ranges and patterns of variability in carbonate chemistry, including pH (7.70–8.33), pCO2 (172–952 µatm), and the aragonite saturation state, $Ømega$Ar (0.94–3.91).
The ocean is a substantial sink for atmospheric carbon dioxide (CO2) released as a result of human activities. Over the coming decades the dissolved inorganic C concentration in the surface ocean is predicted to increase, which is expected to have a direct influence on the efficiency of C utilization (consumption and production) by phytoplankton during photosynthesis. Here, we evaluated the generality of C‐rich organic matter production by examining the elemental C:N ratio of organic matter produced under conditions of varying pCO2.
Corals build their skeletons using extracellular calcifying fluid located in the tissue-skeleton interface. However, the mechanism by which corals control the transport of calcium and other ions from seawater and the mechanism of constant alkalization of calcifying fluid are largely unknown. To address these questions, we performed direct pH imaging at calcification sites (subcalicoblastic medium, SCM) to visualize active pH upregulation in live aposymbiotic primary coral polyps treated with HCl-acidified seawater.
Understanding functional trait distributions among organisms can inform impacts on and responses to environmental change. In marine systems, only 1% of dissolved inorganic carbon in seawater exists as CO2. Thus the majority of marine macrophytes not only passively access CO2 for photosynthesis, but also actively transport CO2 and the more common bicarbonate (HCO3-, 92% of seawater dissolved inorganic carbon) into their cells.
Ocean acidification threatens many marine organisms, especially marine calcifiers. The only global‐scale solution to ocean acidification remains rapid reduction in CO2 emissions. Nevertheless, interest in localized mitigation strategies has grown rapidly because of the recognized threat ocean acidification imposes on natural communities, including ones important to humans. Protection of seagrass meadows has been considered as a possible approach for localized mitigation of ocean acidification due to their large standing stocks of organic carbon and high productivity.
Based on a survey conducted from June to July 2013, aragonite saturation state variation and control in the river-dominated marginal BoHai and Yellow seas were investigated. Surface water $Ømega$arag ranged from 2.0–3.8, whereas subsurface water $Ømega$arag was generally lower than 2.0. Temperature changes had a strong influence on $Ømega$arag through induced CO2 solubility changes in seawater. Riverine freshwater input decreased $Ømega$arag in the Changjiang and Yalu river estuaries, but induced higher $Ømega$arag in the Yellow River estuary.
Oceans worldwide are undergoing acidification due to the penetration of anthropogenic CO2 from the atmosphere1,2,3,4. The rate of acidification generally diminishes with increasing depth. Yet, slowing down of the thermohaline circulation due to global warming could reduce the pH in the deep oceans, as more organic material would decompose with a longer residence time. To elucidate this process, a time-series study at a climatically sensitive region with sufficient duration and resolution is needed.
Increasing CO2 in seawater (i.e. ocean acidification) may have various and potentially adverse effects on phytoplankton dynamics and hence the organic carbon dynamics. We conducted a CO2 manipulation experiment in the Sea of Okhotsk in summer 2006 to investigate the response of the organic carbon dynamics.
Puget Sound is a large estuary complex in the U.S. Pacific Northwest that is home to a diverse and economically important ecosystem threatened by anthropogenic impacts associated with climate change, urbanization, and ocean acidification. While ocean acidification has been studied in oceanic waters, little is known regarding its status in estuaries. Anthropogenically acidified coastal waters upwelling along the western North American continental margin can enter Puget Sound through the Strait of Juan de Fuca.
Recent observations of calcium carbonate (CaCO3) mineral undersaturations on the Bering Sea Shelf have prompted new interest in the physical and biological factors that control the inorganic carbon system in the region. Understanding of the dynamics that influence the spatio-temporal variability of total alkalinity (TA) – one major component of the seawater carbonate system – has been constrained by limited historical data collected across the shelf, and the consensus has been that TA is largely conservative.
Ocean acidification driven by absorption of anthropogenic carbon dioxide (CO2) from the atmosphere is now recognized as a systemic, global process that could threaten diverse marine ecosystems and a number of commercially important species. The change in calcium carbonate (CaCO3) mineral saturation states (omega) brought on by the reduction of seawater pH is most pronounced in high latitude regions where unique biogeochemical processes create an environment more susceptible to the suppression of omega values for aragonite and calcite, which are critical to shell building organisms.
This investigation reports, for the first time, results of CO2 system variables in the Gulf of Tehuantepec, located in the Mexican tropical Pacific. We quantified the post-Tehuano concentration of dissolved inorganic carbon (DIC) and pH (April 2013). These values were used to calculate pCO2, aragonite saturation ($Ømega$Ar), and air-sea CO2 fluxes (FCO2). The intense vertical stratification was found to contribute to the biogeochemical processes in surface waters (\textless70 m).