The boron isotopic ($δ$11Bcarb) compositions of long-lived Porites coral are used to reconstruct reef-water pH across the central Great Barrier Reef (GBR) and assess the impact of river runoff on inshore reefs. For the period from 1940 to 2009, corals from both inner- and mid-shelf sites exhibit the same overall decrease in $δ$11Bcarb of 0.086 ± 0.033‰ per decade, equivalent to a decline in seawater pH (pHsw) of ̃0.017 ± 0.007 pH units per decade.
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.
The Chilean Patagonia constitutes one of the most important and extensive fjord systems worldwide, therefore can be used as a natural laboratory to elucidate the pathway of both organic and inorganic matter in the receiving environment. In this study we use data collected during an intensive oceanographic cruise along the Magellan Strait into the Almirantazgo Fjord in southern Patagonia to evaluate how different sources of dissolved inorganic carbon (DIC) and recycling may impact particulate organic carbon (POC) $δ$13C and influence the nutrients and carbonate system spatial distribution.
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.
Freshwater discharge affects the biogeochemistry of river-influenced nearshore environments by contributing with carbon and nutrients. An increase in human activities in river basins may alter the natural riverine nutrients and carbon export to coastal ecosystems. Along a wide latitudinal range (32°55′S–40°10′S), this study explores the role of climate and land use in determining the nutrient and carbon concentrations in the river mouth and fluxes to adjacent coastal areas.
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.
Anthropogenic CO2 is causing warming and ocean acidification. Coral reefs are being severely impacted, yet confusion lingers regarding how reefs will respond to these stressors over this century. Since the 1982-83 El Niño-Southern Oscillation warming event, the persistence of reefs around the Galápagos Islands has differed across an acidification gradient. Reefs disappeared where pH \textless 8.0 and aragonite saturation state ($Ømega$arag) ≤ 3 and have not recovered, whereas one reef has persisted where pH \textgreater 8.0 and $Ømega$arag \textgreater 3.
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).