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Abstract The removal of carbon dioxide from the atmosphere by the marine biological pump is a key regulator of Earth’s climate; however, the ocean also serves as a large source of nitrous oxide, a potent greenhouse gas and ozone-depleting substance. Although biological carbon sequestration and nitrous oxide production have been individually studied in the ocean, their combined impacts on net greenhouse forcing remain uncertain. Here we show that the magnitude of nitrous oxide production in the epipelagic zone of the subtropical ocean covaries with remineralization processes and thus acts antagonistically to weaken the radiative benefit of carbon removal by the marine biological pump. Carbon and nitrogen isotope tracer incubation experiments and nitrogen isotope natural abundance data indicate enhanced biological activity promotes nitrogen recycling, leading to substantial nitrous oxide production via both oxidative and reductive pathways. These shallow-water nitrous oxide sources account for nearly half of the air–sea flux and counteract 6–27% (median 9%) of the greenhouse warming mitigation achieved by carbon export via the biological pump. 

In this paper, we outline the need for a coordinated international effort toward the building of an open-access Global Ocean Oxygen Database and ATlas (GO 2 DAT) complying with the FAIR principles (Findable, Accessible, Interoperable, and Reusable). GO 2 DAT will combine data from the coastal and open ocean, as measured by the chemical Winkler titration method or by sensors (e.g., optodes, electrodes) from Eulerian and Lagrangian platforms (e.g., ships, moorings, profiling floats, gliders, ships of opportunities, marine mammals, cabled observatories). GO 2 DAT will further adopt a community-agreed, fully documented metadata format and a consistent quality control (QC) procedure and quality flagging (QF) system. GO 2 DAT will serve to support the development of advanced data analysis and biogeochemical models for improving our mapping, understanding and forecasting capabilities for ocean O 2 changes and deoxygenation trends. It will offer the opportunity to develop quality-controlled data synthesis products with unprecedented spatial (vertical and horizontal) and temporal (sub-seasonal to multi-decadal) resolution. These products will support model assessment, improvement and evaluation as well as the development of climate and ocean health indicators. They will further support the decision-making processes associated with the emerging blue economy, the conservation of marine resources and their associated ecosystem services and the development of management tools required by a diverse community of users (e.g., environmental agencies, aquaculture, and fishing sectors). A better knowledge base of the spatial and temporal variations of marine O 2 will improve our understanding of the ocean O 2 budget, and allow better quantification of the Earth’s carbon and heat budgets. With the ever-increasing need to protect and sustainably manage ocean services, GO 2 DAT will allow scientists to fully harness the increasing volumes of O 2 data already delivered by the expanding global ocean observing system and enable smooth incorporation of much higher quantities of data from autonomous platforms in the open ocean and coastal areas into comprehensive data products in the years to come. This paper aims at engaging the community (e.g., scientists, data managers, policy makers, service users) toward the development of GO 2 DAT within the framework of the UN Global Ocean Oxygen Decade (GOOD) program recently endorsed by IOC-UNESCO. A roadmap toward GO 2 DAT is proposed highlighting the efforts needed (e.g., in terms of human resources). 

Abstract Mesoscale eddies may enhance nutrient injection into the photic zone and ultimately the magnitude and composition of particle export to depth. Using satellite altimetry, we identified 38 cyclonic eddies that passed in close proximity to the Hawaii Ocean Time‐series (HOT) Station ALOHA, located in the North Pacific Subtropical Gyre, from 1993 to 2018. Particulate carbon (C), nitrogen (N), and biogenic silica (Si) export rates, measured using free floating sediment traps deployed at 150 m as part of HOT, were then associated with either the eddy core or edge based on distance to the eddy center and time of eddy evolution. Elemental fluxes varied significantly within and among individual eddies depending on season and eddy age. Spatially, biogenic Si fluxes were enhanced relative to particulate C and N fluxes at both the cores and edges, with temporally highest particulate C, N and biogenic Si fluxes occurring during the mature stage (3–8 weeks). On average, biogenic Si fluxes were 200 ± 80% (30–270% increase) higher relative to non‐eddy and during non‐bloom periods, with modest enhanced particulate C (10–30% increase) and N (10–20% increase) fluxes. In contrast, during the bloom season (July and August), elemental fluxes were all reduced by 20% relative to non‐eddy references, suggesting that cyclonic eddies depress export during the bloom period. Our results indicate that cyclonic eddies not only increase, but differentially impact the sinking export of critical biological elements, thereby contributing to long term ecological changes in foodwebs that rely on silica as well as carbon for growth. 

Abstract Global carbon dioxide (CO₂) evasion from inland waters (rivers, lakes, and reservoirs) and carbon (C) export from land to oceans constitute critical terms in the global C budget. However, the magnitudes, spatiotemporal patterns, and underlying mechanisms of these fluxes are poorly constrained. Here, we used a coupled terrestrial–aquatic model to assess how multiple changes in climate, land use, atmospheric CO₂concentration, nitrogen (N) deposition, N fertilizer and manure applications have affected global CO₂evasion and riverine C export along the terrestrial‐aquatic continuum. We estimate that terrestrial C loadings, riverine C export, and CO₂evasion in the preindustrial period (1800s) were 1,820 ± 507 (mean ± standard deviation), 765 ± 132, and 841 ± 190 Tg C yr⁻¹, respectively. During 1800–2019, multifactorial global changes caused an increase of 25% (461 Tg C yr⁻¹) in terrestrial C loadings, reaching 2,281 Tg C yr⁻¹in the 2010s, with 23% (104 Tg C yr⁻¹) of this increase exported to the ocean and 59% (273 Tg C yr⁻¹) being emitted to the atmosphere. Our results showed that global inland water recycles and exports nearly half of the net land C sink into the atmosphere and oceans, highlighting the important role of inland waters in the global C balance, an amount that should be taken into account in future C budgets. Our analysis supports the view that a major feature of the global C cycle–the transfer from land to ocean–has undergone a dramatic change over the last two centuries as a result of human activities.