Coastal Carbon Budgets Research Articles

Carbon export from submarine groundwater discharge in a semi-enclosed bay: Impact for the buffering capacity against coastal ocean acidification

Submarine groundwater discharge (SGD) serves as an important pathway for the transport of dissolved carbon from land to ocean, significantly affecting the coastal biogeochemical cycles. However, the impact of SGD-derived dissolved carbon on the coastal carbon budget remains poorly understood. This study first quantified SGD and associated dissolved organic carbon (DOC), dissolved inorganic carbon (DIC) and total alkalinity (TA) fluxes in Daya Bay using mass balance models based on radium isotopes (223Ra, 224Ra, 226Ra and 228Ra). We then constructed carbon mass balance models to evaluate the impact of SGD-derived carbon on the buffering capacity against coastal ocean acidification. The estimated SGD fluxes ranged from 0.80 × 107 to 2.64 × 107 m3d−1. The DIC, DOC and TA fluxes from SGD were 17.90–36.44 mmol m−2d−1, 0.93–2.13 mmol m−2d−1, and 21.19–28.47 mmol m−2d−1, respectively. Based on carbon mass balances, the DIC flux from SGD was 19–39 times the riverine input, accounting for 27.16 % ∼ 37.64 % of the total carbon source. These results suggest that SGD is a major contributor to DIC, significantly affecting the coastal carbon budget. Furthermore, the average TA:DIC ratio of groundwater discharging into Daya Bay was approximately 1.13. High TA exports enhance the buffering capacity of the coastal ocean and contribute bicarbonate to the ocean, playing a significant role in the ocean carbon sequestration process. This study demonstrates the importance of SGD-derived dissolved carbon in the assessment of coastal carbon budgets.

Toward the future integration of land-to-ocean observing systems to characterize organic carbon fluxes from storms

Storms can drive massive fluxes of carbon from land to ocean via rivers, contributing a large but relatively uncertain term to coastal carbon budgets. To estimate storm-driven aquatic organic carbon fluxes and develop a framework for future observations, we conducted a case study of extreme precipitation followed by river discharge to the Chesapeake Bay watershed, on the east coast of the United States over two decades from June 2001 to July 2021. Anomalous high precipitation events were defined as the top 5% of five-day accumulated precipitation over the watershed and we identified 80 distinct large storms over the Chesapeake Bay region. The top 1% of five-day accumulated river discharge from the United States Geological Survey (USGS) gage stations provided secondary storm criteria to distinguish extreme precipitation that manifest in very high flow: over the same period, we identified 16 storms that led to very high streamflow and combined streamflow with observations of POC and DOC to estimate daily mass flux from the seven major rivers. An extremely large convective storm and subsequent river discharge in July 2018 was studied to determine the association between precipitation, river discharge, and satellite ocean color in combination with in situ observations. MODIS-Aqua satellite derived dissolved organic carbon (DOC) concentration was calculated for all images in 2004–2021 and the estimated DOC values in 2018 were used to assess the feasibility of the optical satellites to monitor coastal storm fluxes of carbon. Using the USGS Load Estimator stream flow model and historical observations, the 2018 event exported approximately 12.9 Gg C particulate organic carbon (POC) and 12.5 Gg C DOC into the bay for 7.2% and 4.4% of the annual total, respectively. The largest storm over the last 20 years exported up to 16% of the annual total POC and 11% of the annual total of DOC from the major rivers over 10 days. However, monitoring the evolution of riverine carbon in estuarine environments from optical satellites alone remains challenging due to cloud cover, thus additional observing platforms assimilated through models are essential.

Functioning of a canopy-dominated intertidal community during emersion: highly productive but heterotrophic at the annual scale

In order to address lack of data regarding coastal carbon budgets, we estimated the annual metabolic carbon budget of an intertidal rocky reef macroalgal community during emersion. This budget is based on direct in situ measurements during emersion and establishes the seasonal variations of the photosynthetic parameters of such a community. CO2 fluxes were measured hourly to study the response of community gross primary productivity (GPP) to irradiance and the variation of GPP and community respiration (CR) over the emersion period at different times of the year. These were combined together with existing monthly measures of GPP and CR hourly rates to model the variations of these fluxes as a function of irradiance and the tidal cycle throughout an entire calendar year. Daily, monthly and annual values of GPP, CR and net primary productivity (NPP) were calculated with a relatively low sensitivity to any of the parameters used. While GPP fluxes show comparable orders of magnitude to those measured in other systems, higher CR fluxes lead to a heterotrophic system during emersion, both under measured (NPP = −299 gC m−2 year−1) and theoretical irradiances (NPP = −119 gC m−2 year−1). This heterotrophy is directly linked to the light availability, varying according to combined daily, tidal and seasonal cycles, and to temperature at the seasonal scale. Measurements performed in situ at the community scale integrated interactions that are otherwise absent at the individual scale. This gives access to aspects of the functioning that cannot be otherwise identified.

Dissolved carbon dynamics and exchange in a high permeability beach aquifer

The biogeochemical transformation of dissolved carbon in tidal beaches affects the coastal carbon cycle and budget. Yet, the influence of groundwater flow on the behavior of dissolved carbon and CO2 flux across the different interfaces in these dynamic beach systems remains poorly understood, especially in deep beach aquifers. In this study, we investigated the biogeochemical reactions and origins of dissolved carbon and quantitatively evaluated CO2 outgassing driven by submarine groundwater discharge (SGD) in a high permeability beach aquifer (9–13 m depth) located in the South China Sea shelf. Results revealed that both dissolved inorganic carbon (DIC) and total alkalinity (TA) exhibited non-conservative additions across the salinity gradient. The excess DIC and TA most likely resulted from organic carbon decomposition in the brackish and saline zones. Aerobic respiration (upper saline plume zone), anaerobic reactions, and tidal mixing were identified as the dominant processes controlling DIC and TA dynamics. The mean CO2 outgassing flux across the beach sediment-air interface was estimated to be 1.05 g m−2 d−1, significantly higher than the CO2 flux across the sea-air interface. The outgassing pattern of groundwater CO2 from beach aquifer appeared to be driven by tidal pumping. Considering the combined effects of SGD-derived dissolved carbon and nutrients, we suggest that SGD yielded a net CO2 flux, contributing to 45 % of the CO2 flux across the sea-air interface. SGD directly and indirectly delivered substantial CO2 from the beach aquifer to the atmosphere, approximately (4.89–9.21) × 103 tons of CO2 per year along the 76.2 km long sandy coast. These findings demonstrate that intertidal beach aquifers, as active biogeochemical reactors have the strong potential to intensify CO2 emissions to the atmosphere through both beach sediment-air and sea-air interfaces. This study provides a better understanding of the links between carbon biogeochemical cycles and hydrologic processes in the coastal zones.

Insights into constraining coastal carbon export from radioisotopes

Coastal shelves are important regions for carbon transformation and storage, however, constraining coastal carbon budgets and their uncertainties remains a challenge. Repeated sampling of a semi-restricted coastal basin in Nova Scotia, Canada was performed in 2019 utilizing the 238U-234Th isotope system to estimate carbon flux in both the water column and surface sediments. 234Th fluxes in the Bedford Basin water column appeared to be in relative balance with those arriving at the seafloor averaged over spring and summer. The resulting carbon export estimates averaged ~70 mmol C m-2 d-1 for April through August of 2019 and 234Th-derived annual export estimates (19 mol C m-2 yr-1) were within a factor of three of the model-based estimates for the basin. Incorporating the results from prior research, this study constrains the major carbon sources and sinks in Bedford Basin. While the 238U-234Th method is well-established in the open ocean, its use in coastal shelf regions is still evolving. Pronounced 234Th deficits are unique to coastal zones and continue to raise important questions about the physical and biogeochemical factors that influence tracer distributions and the carbon estimates that are derived from them. Future paths and method refinements for utilizing the 238U-234Th system in coastal regions are put forth here, including the use of size-fractionated sampling, the need for boreal winter estimates, the quantification of horizontal mixing contributions, an analysis of the role of small particles in coastal carbon budgets, and the study of sediment resuspension’s impact on tracer distributions.

Wind-modulated groundwater discharge along a microtidal Arctic coastline

Groundwater discharge transports dissolved constituents to the ocean, affecting coastal carbon budgets and water quality. However, the magnitude and mechanisms of groundwater exchange along rapidly transitioning Arctic coastlines are largely unknown due to limited observations. Here, using first-of-its-kind coastal Arctic groundwater timeseries data, we evaluate the magnitude and drivers of groundwater discharge to Alaska’s Beaufort Sea coast. Darcy flux calculations reveal temporally variable groundwater fluxes, ranging from −6.5 cm d−1 (recharge) to 14.1 cm d−1 (discharge), with fluctuations in groundwater discharge or aquifer recharge over diurnal and multiday timescales during the open-water season. The average flux during the monitoring period of 4.9 cm d−1 is in line with previous estimates, but the maximum discharge exceeds previous estimates by over an order-of-magnitude. While the diurnal fluctuations are small due to the microtidal conditions, multiday variability is large and drives sustained periods of aquifer recharge and groundwater discharge. Results show that wind-driven lagoon water level changes are the dominant mechanism of fluctuations in land–sea hydraulic head gradients and, in turn, groundwater discharge. Given the microtidal conditions, low topographic relief, and limited rainfall along the Beaufort Sea coast, we identify wind as an important forcing mechanism of coastal groundwater discharge and aquifer recharge with implications for nearshore biogeochemistry. This study provides insights into groundwater flux dynamics along this coastline over time and highlights an oft overlooked discharge and circulation mechanism with implications towards refining solute export estimates to coastal Arctic waters.

Intermittent Upwelling Events Trigger Delayed, Major, and Reproducible Pico‐Nanophytoplankton Responses in Coastal Oligotrophic Waters

AbstractPico‐nanophytoplankton organisms are dominant in oceanic oligotrophic areas but their adaptive growth rates make their contribution to the carbon cycle difficult to estimate. Here we address their response capacities after sporadic wind gusts causing upwelling events in a coastal Mediterranean station. When the water column is stratified, corresponding to oligotrophic conditions, these events generate intense short‐lived nutrient pulses and seawater temperature drops lasting 6 days on average with decreases up to 10°C. Using an automated flow cytometer and statistical rupture‐detection methods, we characterize the responses of five pico‐nanophytoplankton functional groups at a two‐hour frequency from September 2019 to November 2021. These events trigger delayed increases in both abundances and biomasses following similar patterns for most groups that can overpass spring bloom values, and are immediately followed by an overall decrease, suggesting a clear physical driver. These submesoscale events, due to their short duration, are poorly represented in coastal carbon budgets.

Temporal dynamics of lateral carbon export from an onshore aquaculture farm

Many coastal areas are hotspots of aquaculture expansion, where the overuse of artificial feeds results in the accumulation of organic carbon in nearshore aquaculture ponds. In rural areas, wastewater from the aquaculture ponds is discharged to the nearshore waters through artificial ditches causing lateral carbon export from the land to the ocean. Such flux may be meaningful in coastal carbon budgets since aquaculture is the hotspot of carbon sequestration and storage. To quantify the magnitude and temporal dynamics of lateral carbon export from aquaculture ponds, we used high-frequency in-situ monitoring of turbidity, fluorescent dissolved organic matter, etc. across different temporal scales. We measured water levels and velocity profiles in a ditch cross-section to obtain year-round water exchange. Carbon export was integrated from water fluxes and organic carbon concentrations. Our results suggested that aquaculture ponds were a source of particular organic carbon (POC) and dissolved organic carbon (DOC). The net lateral flux of POC and DOC was 148 ± 38 kg yr−1 and 296 ± 18 kg yr−1. Temporally, the export of POC and DOC is influenced by both tides and wastewater discharge. Under the disturbance with aquaculture wastewater discharge, the mean DOC export in the ditch increased by 497 kg, which was 1.5 times that of the undisturbed; the mean POC export increased by 190 kg, which was 1.8 times that of the undisturbed. Thus, aquaculture activities can considerably disturb the coastal carbon balance by facilitating carbon-rich fluid exchange from onshore farms to nearshore estuaries. As aquaculture expands across Asia and the globe, this study provides important insights into the impacts of aquaculture on coastal carbon budgets.

Fossilized diatoms as indirect indicators of the origin of carbon stored in intertidal flats

Coastal systems store enormous carbon quantities in their sediment, which originates from various autochthonous and allochthonous sources. Carbon fluxes in coastal ecosystems have a strong effect on the recipient food-webs and carbon emission offsets. Yet, the relative importance of autochthonous vs. allochthonous C inputs to coastal carbon budget is still challenging to identify. Here, we combine diatoms preserved in the sediment with geochemical analyses to identify the sources of carbon stored in Africa’s largest intertidal seagrass beds at Banc d’Arguin, Mauritania. The area lies between an active ocean upwelling and the ‘Sahara-dust hotspot’ systems. The extensive seagrass beds of the area are thus expected to receive C from these neighboring systems in addition to producing C in-situ. Three sediment cores (50 cm) were collected at three intertidal sites with different hydrodynamic regimes, and analyzed for diatom composition, total organic carbon (TOC), total nitrogen (TN), total phosphorus (TP), and carbon isotopic signatures (δ13C). Diatom taxa are grouped into three guilds: (1) benthic (epiphyte, epipelon, and epipsammon), (2) planktonic, and (3) freshwater. Benthic diatoms are considered to be autochthonous, while typical oceanic and freshwater diatoms are considered to be allochthonous. Benthic diatoms are the most diverse and abundant group, while allochthonous freshwater (i.e., dust imported) and typical upwelling (i.e., tidal imported) taxa ranked last in both abundance and species’ richness. Structure equation modelling shows that variation in the stored carbon is best explained by the total abundance of diatoms and guild composition. We conclude that the C stored in the intertidal seagrass beds of Banc d’Arguin is predominantly autochthonous. Our method provides an effective way to identify historical carbon sources in coastal systems.

Sources, spectral characteristics, and fluxes of dissolved organic matter in coastal groundwater and river water in western Guangdong, China

Groundwater discharge and river runoff are two important ways for allochthonous dissolved organic matter (DOM) to enter the ocean, but they vary spatially. Currently, the source, composition, and efflux of groundwater and riverine dissolved organic matter to the tropical northern South China Sea remain poorly understood, preventing an accurate estimate of coastal carbon budgets. In July 2021, nine groundwater and six river water samples were collected along the coast of western Guangdong and were characterized using dissolved organic carbon (DOC) analysis, UV-visible, and fluorescence spectroscopy techniques. Atypical absorption spectra were strongly observed in groundwaters, which were mainly attributed to the high-level nitrates. An exponential-Gaussian equation showed that the average contribution of nitrate to total groundwater absorbances was up to 36% at ∼ 300 nm. Groundwater showed lower levels of DOC, colored dissolved organic matter (CDOM), and fluorescent dissolved organic matter (FDOM) as compared to river water, whereas the humic-like components dominated both groundwater and river water FDOM pools. Higher values of spectral slope S350–400, fluorescence index, biological index, and the ratio of two humic-like fluorescence jointly reveal that groundwater DOM mainly originated from microbial activities, whereas the river water DOM had considerable contribution from terrestrial soil. High precipitation, natural or agricultural land types, and a lack of seawater intrusion are expected to cause low levels of groundwater DOM in western Guangdong. Among 52 rivers from across the globe, high watershed productivity and precipitation may lead to high–moderate DOM levels in river water in western Guangdong. The DOM fluxes via fresh groundwater discharge in western Guangdong are comparable in magnitude to those by river runoff, accounting for 16%–18% of the Pearl River DOM fluxes. Based on the slopes of linear correlations between CDOM and DOC obtained in groundwater samples and 52 rivers, as well as the data on water fluxes and DOC levels, the global CDOM fluxes via groundwater discharge and river runoff are estimated to be 3.5–12.2 × 1012 m2 yr−1 and 4.3 ± 0.3 × 1014 m2 yr−1, respectively, highlighting the importance of considering groundwater discharge and river runoff in coastal carbon budgets.

Submarine Groundwater Discharge in the Northern Bohai Sea, China: Implications for Coastal Carbon Budgets and Buffering Capacity

AbstractSubmarine groundwater discharge (SGD) has been widely recognized as an important source of dissolved nutrients in coastal waters and affects nutrient biogeochemistry. In contrast, little information is available on SGD impacts on coastal carbon budgets. Here, we assessed the SGD and associated carbon (dissolved inorganic carbon [DIC] and total alkalinity [TA]) fluxes in Liaodong Bay (the largest bay of the Bohai Sea, China) and discussed their border implications for coastal DIC budget and buffering capacity. Based on 223Ra and 228Ra mass balance models, the SGD flux was estimated to be (0.92–1.43) × 109 m3 d−1. SGD was the largest contributor of DIC, accounting for 55%–77% of the total DIC sources. The low ratio (<1) of SGD‐derived TA to DIC fluxes and negative correlation between radium isotopes and pH in seawater implied that SGD would potentially reduce seawater pH in Liaodong Bay. Combining the groundwater carbon data in Liaodong Bay with literature data, we found that the SGD‐derived DIC flux off China was 4–9 times greater than those from rivers. By analyzing the TA/DIC ratios in groundwater along the Chinese coast and related carbon fluxes, SGD was thought to partially reduce the CO2 buffer capacity in receiving seawater. These results obtained at the bay scale and national scale suggest that SGD is a significant component of carbon budget and may play a critical role in modulating coastal buffering capacity and atmospheric CO2 sequestration.

Strong Dynamics in Tidal Marsh DOC Export in Response to Natural Cycles and Episodic Events From Continuous Monitoring

AbstractThe role of tidal wetlands as hotspots for carbon and nutrient exchange with adjacent waters has been well documented, but large uncertainties remain regarding the physical and biogeochemical controls on these fluxes, which have significant implications for coastal carbon cycling and budgets. This study elucidates the variability in lateral wetland dissolved organic (DOC) fluxes tidally, seasonally, and during extreme weather events for a brackish wetland within a sub‐estuary of the northwestern Chesapeake Bay, USA. Continuous fluxes from the wetland‐draining tidal creek were calculated based on DOC concentrations ([DOC]) estimated using optical and physicochemical properties measured in situ with concurrent water flow data. Mean export was found to be 8.59 (±1.20) kg C (n = 1,128) tidal cycle−1 and annual flux from the wetland to sub‐estuary was 200.66 (±28.09) g C m−2 yr−1. Peaks in DOC flux were associated with Hurricane Joaquin in 2015, where just two tidal cycles accounted for ∼5% of annual export. Analysis of tidal creek water quality measurements reveal seasonal and tidal dependencies. Highest [DOC] and largest low versus high tide differences were observed in summer, corresponding to more fresh plant biomass and its mobilization, consistent with results from Fourier transform ion cyclotron resonance mass spectrometry. Despite summer highs in tidal creek [DOC], monthly DOC fluxes were greatest in early fall due to higher water flows. The annual flux presented here is higher than fluxes previously reported for this system, highlighting the importance of continuous measurements for monitoring carbon export under a wide range of environmental conditions.

Geochemical characteristics of strontium isotopes in a coastal watershed: implications for anthropogenic influenced chemical weathering and export flux.

Coastal watershed are essential in transporting dissolved loads from terrestrial biogeochemical process of surface environment to the adjacent oceans. The solute chemistry of coastal river water contains significant information about environmental processes under the impact of both natural lithology and anthropogenic pressure. In this study, strontium (Sr) isotopes and water chemistry data of the Jiulongjiang (JLJ) river water were analyzed in detail to trace the contribution of bedrock weathering, and quantify Sr flux to the East China Sea (ECS). The dissolved Sr contents ranged 0.07–0.90 μmol L−1 and greatly fluctuated where tributaries encountered, and 87Sr/86Sr values relatively fluctuated between 0.7140 and 0.7514. Silicate weathering was identified to be the predominant contribution of riverine dissolved loads. Strontium flux to the ocean in dry season was estimated to be 689.2 tons per year, implying an essential influence on oceanic strontium evolution. In accordance with forward model, the silicate weathering rate and CO2 consumption rate were 55.7 tons km−2 per year and 16.9 × 105 mol km−2 per year, respectively, slightly higher than world average. Considering anthropogenic impacts alongside the river, the integrated effect of lower runoff and longer retention time of river water in dry season may aggravate weathering processes. Although CO2 sink by silicate weathering in JLJ seems less than the sink in world’s central reservoirs, it should still be taken into consideration for coastal carbon budget. These findings highlight the use of geochemical characteristics of strontium and its isotopes in identifying weathering process and output flux to the ocean, which provides basic data for sustainable coastal water resource management.

Submarine Groundwater and River Discharges Affect Carbon Cycle in a Highly Urbanized and River-Dominated Coastal Area

Riverine carbon flux to the ocean has been considered in estimating coastal carbon budgets, but submarine groundwater discharge (SGD) has long been ignored. In this paper, the effects of both SGD and river discharges on the carbon cycle were investigated in the Guangdong-HongKong-Macao Greater Bay Area (GBA), a highly urbanized and river-dominated coastal area in China. SGD-derived nitrate (NO3–), dissolved organic carbon (DOC), and dissolved inorganic carbon (DIC) fluxes were estimated using a radium model to be (0.73–16.4) × 108 g/d, (0.60–9.94) × 109 g/d, and (0.77–3.29) × 1010 g/d, respectively. SGD-derived DOC and DIC fluxes are ∼2 times as great as riverine inputs, but SGD-derived NO3– flux is one-fourth of the riverine input. The additional nitrate and carbon inputs can stimulate new primary production, enhance biological pump efficiency, and affect the balance of the carbonate system in marine water. We found that SGD in the studied system is a potential net source of atmospheric CO2 with a flux of 1.46 × 109 g C/d, and river, however, is a potential net sink of atmospheric CO2 with a flux of 3.75 × 109 g C/d during the dry winter season. Two conceptual models were proposed illustrating the major potential processes of the carbon cycle induced by SGD and river discharges. These findings from this study suggested that SGD, as important as rivers, plays a significant role in the carbon cycle and should be considered in carbon budget estimations at regional and global scales future.

Degrading permafrost river catchments and their impact on Arctic Ocean nearshore processes

Arctic warming is causing ancient perennially frozen ground (permafrost) to thaw, resulting in ground collapse, and reshaping of landscapes. This threatens Arctic peoples' infrastructure, cultural sites, and land-based natural resources. Terrestrial permafrost thaw and ongoing intensification of hydrological cycles also enhance the amount and alter the type of organic carbon (OC) delivered from land to Arctic nearshore environments. These changes may affect coastal processes, food web dynamics and marine resources on which many traditional ways of life rely. Here, we examine how future projected increases in runoff and permafrost thaw from two permafrost-dominated Siberian watersheds—the Kolyma and Lena, may alter carbon turnover rates and OC distributions through river networks. We demonstrate that the unique composition of terrestrial permafrost-derived OC can cause significant increases to aquatic carbon degradation rates (20 to 60% faster rates with 1% permafrost OC). We compile results on aquatic OC degradation and examine how strengthening Arctic hydrological cycles may increase the connectivity between terrestrial landscapes and receiving nearshore ecosystems, with potential ramifications for coastal carbon budgets and ecosystem structure. To address the future challenges Arctic coastal communities will face, we argue that it will become essential to consider how nearshore ecosystems will respond to changing coastal inputs and identify how these may affect the resiliency and availability of essential food resources.

Reduction in Riverine Freshwater Supply Changes Inorganic and Organic Carbon Dynamics and Air‐Water CO2 Fluxes in a Tropical Mangrove Dominated Estuary

AbstractReduction in riverine freshwater supply due to climate change as well as anthropogenic activities are documented throughout the globe. How river discontinuity in upstream reaches and the subsequent reduction in freshwater influx alter inorganic and organic carbon dynamics in downstream estuaries adjacent to mangroves has been rarely reported. We investigated the dynamics of the inorganic carbon system and organic matter (OM) in two Indian estuaries near mangroves; riverine freshwater supply to the Matla Estuary was reduced and that to the Dhamra Estuary was uninterrupted. Seasonal sampling was conducted over an annual cycle. We used elemental and stable isotope signatures to delineate the sources of OM and dissolved inorganic carbon (DIC). We found that compared to the Dhamra, the reduced riverine freshwater supply to the Matla increased the marine influence in the estuary on the OM degradation pathways and decreased CO2 emissions to the atmosphere. In the Dhamra, higher seasonal variability in biogeochemical pathways, facilitated high internal carbonate buffering capacity; in contrast in the Matla, the greater marine influence increased the carbonate buffering capacity, resulting in retention of higher DIC concentrations and low CO2 emissions. Dissolved and particulate organic carbon concentrations were higher in the Dhamra than the Matla, indicating higher riverine supply of these. The present study can contribute an overlooked effect of long‐term changes in riverine freshwater supply on the carbon dynamics of mangrove‐dominated estuaries, which might help to improve the understanding of coastal carbon budgets in a changing world.

The role of short-term and long-term water level and wave variability in coastal carbon budgets

SummaryWe investigated soil organic carbon dynamics at three freshwater coastal sites in the Laurentian Great Lakes using a simple carbon budget box model. Long-term carbon budgets (1939–2018) were developed using aerial photography and then compared to short-term carbon export (2018–2019) developed using drone data. This study puts forth a refined coastal carbon budget model that advances previous model iterations by: (1) examining spatial variability in carbon budgets, (2) including a temporally dynamic carbon inventory term, and (3) updating the erosional term. Half of the initial carbon stock of the combined sites was lost in the 80-year study period, which is severely imbalanced with the age of those coastal habitats (400–2000 cal years BP). Major periods of carbon loss corresponded to periods of elevated water level. Short-term loss of carbon during 2018–2019 corresponded to northeasterly extreme wave events during a period of above-average water level.

Impact of salinity and carbonate saturation on stable Sr isotopes (δ88/86Sr) in a lagoon-estuarine system

Local carbonate cycling in lagoon-estuarine systems, involving processes such as inorganic and biogenic carbonate precipitation/dissolution, represents an important but poorly constrained component of the coastal carbon budget. This study investigates the sensitivity of stable Sr isotope tracer (δ88/86Sr) with respect to carbonate saturation and salinity of local waters in the Coorong, Lower Lakes and Murray Mouth (CLLMM) estuary in South Australia. The CLLMM has an extensive range of salinity from fresh to hypersaline (from ∼0 to over 100 PSU), with corresponding variations in water chemistry and major ion composition that in turn controls mineral saturation states, and thus CaCO3 precipitation/dissolution in local waters. Here we use the novel δ88/86Sr tracer in tandem with the more established radiogenic Sr isotope ratio (87Sr/86Sr), where the latter is a robust proxy for Sr sources and thus water provenance. We also produced a geochemical (PHREEQC) model of calcium carbonate (CaCO3) saturation changes across this unique lagoon-estuarine system.The results indicate a systematically increasing trend of δ88/86Sr (from ∼0.25‰ to ∼0.45‰) with increasing salinity and CaCO3 (aragonite, calcite) saturation indices of the coastal waters, which in turn suggest an overall control of carbonate dissolution/precipitation processes on the stable Sr isotope composition in the CLLMM system. This was further corroborated by Ca isotope data (δ44/40Ca) published previously on the same samples from the Coorong, as well as a quantitative simulation of local carbonate removal in the lagoon based on Rayleigh modelling and Sr isotope data.Overall, our results confirm that a coupled Sr isotope approach (combining 87Sr/86Sr and δ88/86Sr) can be used to constrain not only the main water sources (continental versus marine Sr) but also local CaCO3 dissolution/precipitation processes, and thus inorganic carbon and coastal carbonate cycling in the CLLMM system. Finally, this coupled δ88/86Sr and 87Sr/86Sr approach can be potentially applied to fossil carbonate archives to reconstruct paleo-hydrology and salinity changes in the CLLMM and/or other carbonate-producing coastal systems.

Large CO2 release and tidal flushing in salt marsh crab burrows reduce the potential for blue carbon sequestration

AbstractAbundant crab burrows in carbon‐rich, muddy salt marsh soils act as preferential water flow conduits, potentially enhancing carbon transport across the soil–water interface. With increasing recognition of blue carbon systems (salt marshes, mangroves, and seagrass) as hotspots of soil carbon sequestration, it is important to understand drivers of soil carbon cycling and fluxes. We conducted field observations and flow modeling to assess how crab burrows drive carbon exchange over time scales of minutes to weeks in an intertidal marsh in South Carolina. Results showed that continuous advective porewater exchange between the crab burrows and the surrounding soil matrix occurs because of tidally driven hydraulic gradients. The concentrations of dissolved inorganic (DIC) and organic (DOC) carbon in crab burrow porewater differ with that in the surrounding soil matrix, implying a diffusive C flux in the low‐permeability marsh soil. Gas‐phase concentrations of CO2 in ∼ 300 crab burrows were approximately six times greater than ambient air. The estimated total C export rate via porewater exchange (1.0 ± 0.7 g C m−2 d−1) was much greater than via passive diffusion transport (6.7 ± 2 mg C m−2 d−1) and gas‐phase CO2 release (0.93 mg C m−2 d−1). The burrow‐related carbon export was comparable to the regional salt marsh DIC export, groundwater‐derived DIC export, and the net primary production previously estimated using ecosystem‐scale approaches. These insights reveal how crab burrows modify blue carbon sequestration in salt marshes and contribute to coastal carbon budgets.

Relative impacts of global changes and regional watershed changes on the inorganic carbon balance of the Chesapeake Bay

Abstract. The Chesapeake Bay is a large coastal-plain estuary that has experienced considerable anthropogenic change over the past century. At the regional scale, land-use change has doubled the nutrient input from rivers and led to an increase in riverine carbon and alkalinity. The bay has also experienced global changes, including the rise of atmospheric temperature and CO2. Here we seek to understand the relative impact of these changes on the inorganic carbon balance of the bay between the early 1900s and the early 2000s. We use a linked land–estuarine–ocean modeling system that includes both inorganic and organic carbon and nitrogen cycling. Sensitivity experiments are performed to isolate the effect of changes in (1) atmospheric CO2, (2) temperature, (3) riverine nitrogen loading and (4) riverine carbon and alkalinity loading. Specifically, we find that over the past century global changes have increased ingassing by roughly the same amount (∼30 Gg-C yr−1) as has the increased riverine loadings. While the former is due primarily to increases in atmospheric CO2, the latter results from increased net ecosystem production that enhances ingassing. Interestingly, these increases in ingassing are partially mitigated by increased temperatures and increased riverine carbon and alkalinity inputs, both of which enhance outgassing. Overall, the bay has evolved over the century to take up more atmospheric CO2 and produce more organic carbon. These results suggest that over the past century, changes in riverine nutrient loads have played an important role in altering coastal carbon budgets, but that ongoing global changes have also substantially affected coastal carbonate chemistry.