skip to main content


Title: Carbonate Chemistry and the Potential for Acidification in Georgia Coastal Marshes and the South Atlantic Bight, USA
Abstract

In coastal regions and marginal bodies of water, the increase in partial pressure of carbon dioxide (pCO2) in many instances is greater than that of the open ocean due to terrestrial (river, estuarine, and wetland) influences, decreasing buffering capacity and/or increasing water temperatures. Coastal oceans receive freshwater from rivers and groundwater as well as terrestrial-derived organic matter, both of which have a direct influence on coastal carbonate chemistry. The objective of this research is to determine if coastal marshes in Georgia, USA, may be “hot-spots” for acidification due to enhanced inorganic carbon sources and if there is terrestrial influence on offshore acidification in the South Atlantic Bight (SAB). The results of this study show that dissolved inorganic carbon (DIC) and total alkalinity (TA) are elevated in the marshes compared to predictions from conservative mixing of the freshwater and oceanic end-members, with accompanying pH around 7.2 to 7.6 within the marshes and aragonite saturation states (ΩAr) <1. In the marshes, there is a strong relationship between the terrestrial/estuarine-derived organic and inorganic carbon and acidification. Comparisons of pH, TA, and DIC to terrestrial organic material markers, however, show that there is little influence of terrestrial-derived organic matter on shelf acidification during this period in 2014. In addition, ΩArincreases rapidly offshore, especially in drier months (July). River stream flow during 2014 was anomalously low compared to climatological means; therefore, offshore influences from terrestrial carbon could also be decreased. The SAB shelf may not be strongly influenced by terrestrial inputs to acidification during drier than normal periods; conversely, shelf waters that are well-buffered against acidification may not play a significant role in mitigating acidification within the Georgia marshes.

 
more » « less
Award ID(s):
1832178
NSF-PAR ID:
10462001
Author(s) / Creator(s):
; ; ; ; ; ;
Publisher / Repository:
Springer Science + Business Media
Date Published:
Journal Name:
Estuaries and Coasts
Volume:
47
Issue:
1
ISSN:
1559-2723
Format(s):
Medium: X Size: p. 76-90
Size(s):
["p. 76-90"]
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Coastal ecosystems are highly dynamic areas for carbon cycling and are likely to be negatively impacted by increasing ocean acidification. This research focused on dissolved inorganic carbon (DIC) and total alkalinity (TA) in the Mississippi Sound to understand the influence of local rivers on coastal acidification. This area receives large fluxes of freshwater from local rivers, in addition to episodic inputs from the Mississippi River through a human‐built diversion, the Bonnet Carré Spillway. Sites in the Sound were sampled monthly from August 2018 to November 2019 and weekly from June to August 2019 in response to an extended spillway opening. Prior to the 2019 spillway opening, the contribution of the local, lower alkalinity rivers to the Sound may have left the study area more susceptible to coastal acidification during winter months, with aragonite saturation states (Ωar) < 2. After the spillway opened, despite a large increase in TA throughout the Sound, aragonite saturation states remained low, likely due to hypoxia and increased CO2concentrations in subsurface waters. Increased Mississippi River input could represent a new normal in the Sound's hydrography during spring and summer months. The spillway has been utilized more frequently over the last two decades due to increasing precipitation in the Mississippi River watershed, which is primarily associated with climate change. Future increases in freshwater discharge and the associated declines in salinity, dissolved oxygen, and Ωarin the Sound will likely be detrimental to oyster stocks and the resilience of similar ecosystems to coastal acidification.

     
    more » « less
  2. Abstract Estuaries may be uniquely susceptible to the combined acidification pressures of atmospherically driven ocean acidification (OA), biologically driven CO 2 inputs from the estuary itself, and terrestrially derived freshwater inputs. This study utilized continuous measurements of total alkalinity (TA) and the partial pressure of carbon dioxide (pCO 2 ) from the mouth of Great Bay, a temperate northeastern U.S. estuary, to examine the potential influences of endmember mixing and biogeochemical transformation upon estuary buffering capacity ( β – H ). Observations were collected hourly over 28 months representing all seasons between May 2016 and December 2019. Results indicated that endmember mixing explained most of the observed variability in TA and dissolved inorganic carbon (DIC), concentrations of which varied strongly with season. For much of the year, mixing dictated the relative proportions of salinity‐normalized TA and DIC as well, but a fall season shift in these proportions indicated that aerobic respiration was observed, which would decrease β – H by decreasing TA and increasing DIC. However, fall was also the season of weakest statistical correspondence between salinity and both TA and DIC, as well as the overall highest salinity, TA and β – H . Potential biogeochemically driven β – H decreases were overshadowed by increased buffering capacity supplied by coastal ocean water. A simple modeling exercise showed that mixing processes controlled most monthly changes in TA and DIC, obscuring impacts from air–sea exchange or metabolic processes. Advective mixing contributions may be as important as biogeochemically driven changes to observe when evaluating local estuarine and coastal OA. 
    more » « less
  3. A four-decade dataset that spans seven estuaries along a latitudinal gradient in the northwestern Gulf of Mexico and includes measurements of pH and total alkalinity was used to calculate partial pressure of CO 2 ( p CO 2 ), dissolved inorganic carbon (DIC), saturation state of aragonite (Ω Ar ), and a buffer factor (β DIC , which measures the response of proton concentration or pH to DIC concentration change) and examine long-term trends and spatial patterns in these parameters. With the notable exception of the northernmost and southernmost estuaries (and selected stations near freshwater input), these estuaries have generally experienced long-term increases in p CO 2 and decreases in DIC, Ω Ar , and β DIC , with the magnitude of change generally increasing from north to south. At all stations with increasing p CO 2 , the rate of increase exceeded the rate of increase in atmospheric p CO 2 , indicating that these estuaries have become a greater source of CO 2 to the atmosphere over the last few decades. The decreases in Ω Ar have yet to cause Ω Ar to near undersaturation, but even the observed decreases may have the potential to decrease calcification rates in important estuarine calcifiers like oysters. The decreases in β DIC directly indicate that these estuaries have experienced continually greater change in pH in the context of ocean acidification. 
    more » « less
  4. Abstract

    Understanding decadal changes in the coastal carbonate system is essential for predicting how the health of these waters responds to anthropogenic drivers, such as changing atmospheric conditions and riverine inputs. However, studies that quantify the relative impacts of these drivers are lacking. In this study, the primary drivers of decadal trends in the surface carbonate system, and the spatiotemporal variability in these trends, are identified for a large coastal plain estuary: the Chesapeake Bay. Experiments using a coupled three‐dimensional hydrodynamic‐biogeochemical model highlight that, over the past three decades, the changes in the surface carbonate system of Chesapeake Bay have strong seasonal and spatial variability. The greatest surface pH and aragonite saturation state (ΩAR) reductions have occurred in the summer in the middle (mesohaline) Bay: −0.24 and −0.9 per 30 years, respectively, with increases in atmospheric CO2and reductions in nitrate loading both being primary drivers. Reductions in nitrate loading have a strong seasonal influence on the carbonate system, with the most pronounced decadal decreases in pH and ΩARoccurring during the summer when primary production is strongly dependent on nutrient availability. Increases in riverine total alkalinity and dissolved inorganic carbon have raised surface pH in the upper oligohaline Bay, while other drivers such as atmospheric warming and input of acidified ocean water through the Bay mouth have had comparatively minor impacts on the estuarine carbonate system. This work has significant implications for estuarine ecosystem services, which are typically most sensitive to surface acidification in the spring and summer seasons.

     
    more » « less
  5. Abstract

    In estuaries, local processes such as changing material loads from the watershed and complex circulation create dynamic environments with respect to ecosystem metabolism and carbonate chemistry that can strongly modulate impacts of global atmospheric CO2increases on estuarine pH. Long‐term (> 20 yr) surface water pH records from the USA's two largest estuaries, Chesapeake Bay (CB) and Neuse River Estuary‐Pamlico Sound (NRE‐PS) were examined to understand the relative importance of atmospheric forcing vs. local processes in controlling pH. At the estuaries’ heads, pH increases in CB and decreases in NRE‐PS were driven primarily by changing ratios of river alkalinity to dissolved inorganic carbon concentrations. In upper reaches of CB and middle reaches of the NRE‐PS, pH increases were associated with increases in phytoplankton biomass. There was no significant pH change in the lower NRE‐PS and only the polyhaline CB showed a pH decline consistent with ocean acidification. In both estuaries, interannual pH variability showed robust, positive correlations with chlorophylla(Chla) during the spring in mid to lower estuarine regions indicative of strong control by net phytoplankton production. During summer and fall, Chlaand pH negatively correlated in lower regions of both estuaries, given a shift toward heterotrophy driven by changes in phytoplankton community structure and increases in the load ratio of dissolved inorganic nitrogen to organic carbon. Tropical cyclones episodically depressed pH due to vertical mixing of CO2rich bottom waters and post‐storm terrestrial organic matter loading. Local processes we highlight represent a significant challenge for predicting future estuarine pH.

     
    more » « less