Key Points Mackenzie River biogeochemical discharge decreases the southeastern Beaufort Sea carbon sink Terrestrial dissolved inorganic carbon (DIC) is the primary driver of outgassing events in the SBS, followed by terrestrial DOC Interannual variability in river discharge modulates localized air‐sea CO 2 flux
more »
« less
A Numerical reassessment of the Gulf of Mexico carbon system in connection with the Mississippi River and global ocean
Abstract. Coupled physical–biogeochemical models can fill thespatial and temporal gap in ocean carbon observations. Challenges ofapplying a coupled physical–biogeochemical model in the regional oceaninclude the reasonable prescription of carbon model boundary conditions,lack of in situ observations, and the oversimplification of certainbiogeochemical processes. In this study, we applied a coupledphysical–biogeochemical model (Regional Ocean Modelling System, ROMS) to theGulf of Mexico (GoM) and achieved an unprecedented 20-year high-resolution(5 km, 1/22∘) hindcast covering the period of 2000 to 2019. Thebiogeochemical model incorporated the dynamics of dissolved organic carbon(DOC) pools and the formation and dissolution of carbonate minerals. Thebiogeochemical boundaries were interpolated from NCAR's CESM2-WACCM-FV2solution after evaluating the performance of 17 GCMs in the GoM waters. Modeloutputs included carbon system variables of wide interest, such aspCO2, pH, aragonite saturation state (ΩArag), calcitesaturation state (ΩCalc), CO2 air–sea flux, and carbon burialrate. The model's robustness is evaluated via extensive model–datacomparison against buoys, remote-sensing-based machine learning (ML)products, and ship-based measurements. A reassessment of air–sea CO2flux with previous modeling and observational studies gives us confidencethat our model provides a robust and updated CO2 flux estimation, andNGoM is a stronger carbon sink than previously reported. Model resultsreveal that the GoM water has been experiencing a ∼ 0.0016 yr−1 decrease in surface pH over the past 2 decades, accompanied by a∼ 1.66 µatm yr−1 increase in sea surfacepCO2. The air–sea CO2 exchange estimation confirms in accordance with severalprevious models and ocean surface pCO2 observations that theriver-dominated northern GoM (NGoM) is a substantial carbon sink, and theopen GoM is a carbon source during summer and a carbon sink for the rest ofthe year. Sensitivity experiments are conducted to evaluate the impacts ofriver inputs and the global ocean via model boundaries. The NGoM carbonsystem is directly modified by the enormous carbon inputs (∼ 15.5 Tg C yr−1 DIC and ∼ 2.3 Tg C yr−1 DOC) from theMississippi–Atchafalaya River System (MARS). Additionally,nutrient-stimulated biological activities create a ∼ 105 timeshigher particulate organic matter burial rate in NGoM sediment than in thecase without river-delivered nutrients. The carbon system condition of theopen ocean is driven by inputs from the Caribbean Sea via the Yucatan Channeland is affected more by thermal effects than biological factors.
more »
« less
- Award ID(s):
- 1903340
- PAR ID:
- 10438463
- Date Published:
- Journal Name:
- Biogeosciences
- Volume:
- 19
- Issue:
- 18
- ISSN:
- 1726-4189
- Page Range / eLocation ID:
- 4589 to 4618
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Through biological activity, marine dissolved inorganic carbon (DIC) is transformed into different types of biogenic carbon available for export to the ocean interior, including particulate organic carbon (POC), dissolved organic carbon (DOC), and particulate inorganic carbon (PIC). Each biogenic carbon pool has a different export efficiency that impacts the vertical ocean carbon gradient and drives natural air–sea carbon dioxide gas (CO2) exchange. In the Southern Ocean (SO), which presently accounts for ~40% of the anthropogenic ocean carbon sink, it is unclear how the production of each biogenic carbon pool contributes to the contemporary air–sea CO2exchange. Based on 107 independent observations of the seasonal cycle from 63 biogeochemical profiling floats, we provide the basin-scale estimate of distinct biogenic carbon pool production. We find significant meridional variability with enhanced POC production in the subantarctic and polar Antarctic sectors and enhanced DOC production in the subtropical and sea-ice-dominated sectors. PIC production peaks between 47°S and 57°S near the “great calcite belt.” Relative to an abiotic SO, organic carbon production enhances CO2uptake by 2.80 ± 0.28 Pg C y−1, while PIC production diminishes CO2uptake by 0.27 ± 0.21 Pg C y−1. Without organic carbon production, the SO would be a CO2source to the atmosphere. Our findings emphasize the importance of DOC and PIC production, in addition to the well-recognized role of POC production, in shaping the influence of carbon export on air–sea CO2exchange.more » « less
-
Abstract The Arctic Ocean has turned from a perennial ice‐covered ocean into a seasonally ice‐free ocean in recent decades. Such a shift in the air‐ice‐sea interface has resulted in substantial changes in the Arctic carbon cycle and related biogeochemical processes. To quantitatively evaluate how the oceanic CO2sink responds to rapid sea ice loss and to provide a mechanistic explanation, here we examined the air‐sea CO2flux and the regional CO2sink in the western Arctic Ocean from 1994 to 2019 by two complementary approaches: observation‐based estimation and a data‐driven box model evaluation. ThepCO2observations and model results showed that summer CO2uptake significantly increased by about 1.4 ± 0.6 Tg C decade−1in the Chukchi Sea, primarily due to a longer ice‐free period, a larger open area, and an increased primary production. However, no statistically significant increase in CO2sink was found in the Canada Basin and the Beaufort Sea based on both observations and modeled results. The reduced sea ice coverage in summer in the Canada Basin and the enhanced wind speed in the Beaufort Sea potentially promoted CO2uptake, which was, however, counteracted by a rapidly decreased air‐seapCO2gradient therein. Therefore, the current and future Arctic Ocean CO2uptake trends cannot be sufficiently reflected by the air‐seapCO2gradient alone because of the sea ice variations and other environmental factors.more » « less
-
Abstract This contribution to the RECCAP2 (REgional Carbon Cycle Assessment and Processes) assessment analyzes the processes that determine the global ocean carbon sink, and its trends and variability over the period 1985–2018, using a combination of models and observation‐based products. The mean sea‐air CO2flux from 1985 to 2018 is −1.6 ± 0.2 PgC yr−1based on an ensemble of reconstructions of the history of sea surface pCO2(pCO2products). Models indicate that the dominant component of this flux is the net oceanic uptake of anthropogenic CO2, which is estimated at −2.1 ± 0.3 PgC yr−1by an ensemble of ocean biogeochemical models, and −2.4 ± 0.1 PgC yr−1by two ocean circulation inverse models. The ocean also degasses about 0.65 ± 0.3 PgC yr−1of terrestrially derived CO2, but this process is not fully resolved by any of the models used here. From 2001 to 2018, the pCO2products reconstruct a trend in the ocean carbon sink of −0.61 ± 0.12 PgC yr−1 decade−1, while biogeochemical models and inverse models diagnose an anthropogenic CO2‐driven trend of −0.34 ± 0.06 and −0.41 ± 0.03 PgC yr−1 decade−1, respectively. This implies a climate‐forced acceleration of the ocean carbon sink in recent decades, but there are still large uncertainties on the magnitude and cause of this trend. The interannual to decadal variability of the global carbon sink is mainly driven by climate variability, with the climate‐driven variability exceeding the CO2‐forced variability by 2–3 times. These results suggest that anthropogenic CO2dominates the ocean CO2sink, while climate‐driven variability is potentially large but highly uncertain and not consistently captured across different methods.more » « less
-
Arctic landscapes are warming and becoming wetter due to changes in precipitation and the timing of snowmelt which consequently alters seasonal runoff and river discharge patterns. These changes in hydrology lead to increased mobilization and transport of terrestrial dissolved organic matter (DOM) to Arctic coastal seas where significant impacts on biogeochemical cycling can occur. Here, we present measurements of dissolved organic carbon (DOC) and chromophoric DOM (CDOM) in the Yukon River-to-Bering Sea system and two river plumes on the Alaska North Slope which flow into the Beaufort Sea. Our sampling characterized optical and biogeochemical properties of DOM during high and low river discharge periods for the Yukon River-Bering Sea system. The average DOC concentration at the multiple Yukon River mouths ranged from a high of 10.36 mg C L -1 during the ascending limb of the 2019 freshet (late May), 6.4 mg C L -1 during the descending limb of the 2019 freshet (late June), and a low of 3.86 mg C L -1 during low river discharge in August 2018. CDOM absorption coefficient at 412 nm ( a CDOM (412)) averaged 8.23 m -1 , 5.07 m -1 , and 1.9 m -1 , respectively. Several approaches to model DOC concentration based on its relationship with CDOM properties demonstrated cross-system seasonal and spatial robustness for these Arctic coastal systems despite spanning an order of magnitude decrease in DOC concentration from the lower Yukon River to the Northern Bering Sea as well as the North Slope systems. “Snapshot” fluxes of DOC and CDOM across the Yukon River Delta to Norton Sound were calculated from our measurements and modeled water fluxes forced with upstream USGS river gauge data. Our findings suggest that during high river flow, DOM reaches the delta largely unaltered by inputs or physical and biogeochemical processing and that the transformations of Yukon River DOM largely occur in the plume. However, during low summer discharge, multiple processes including local precipitation events, microbial decomposition, photochemistry, and likely others can alter the DOM properties within the lower Yukon River and Delta prior to flowing into Norton Sound.more » « less
An official website of the United States government

