ALBERT

Description: Deoxygenation of the ocean has been occurring over the last half century, particularly in poorly ventilated coastal waters. In coastal and estuarine environments, both the water column and sediments play key roles in controlling oxygen variability. In this study, we focus on controls of oxygen concentration in Bedford Basin (BB), a 70 m deep, seasonally hypoxic semi-enclosed fjord on the West Atlantic coast in Nova Scotia. The basin is connected to the Scotian Shelf via a narrow 20 m deep sill that restricts the resupply of bottom water. Hypoxia was recorded seasonally in 2018, 2019 and 2021 with minimum oxygen concentration of 5, 6.7 and 2.7 μM, respectively. Using a 1-D benthic-pelagic coupled model we investigate oxygen consumption and resupply processes during these years. The model was constrained with weekly water column measurements of temperature, salinity, chlorophyll-a fluorescence and dissolved oxygen from a monitoring station in the central basin together with seasonal measurements of benthic diffusive oxygen uptake. Our model suggested that 29-81%, and up to 36% of bottom water re-oxygenation occurred during the winter mixing period and through summer/fall intrusions of Scotian Shelf water, respectively. Occasional shelf water intrusions occurred rapidly, on a timescale of a few hours, and delivered equivalent amounts of oxygen as winter mixing and were sufficient to end bottom water hypoxia. Collectively, these mechanisms supplied the majority of the oxygen delivered to the bottom water. Oxygen supply to bottom waters during periods of water column stratification accounted for 19-36% of the annual flux. The mean benthic uptake was 12 ± 8 mmol m -2 d -1 and contributed ~20% of the total oxygen consumption below the sill depth. In 2021, sea surface temperature (SST) was unusually high and likely resulted in 50% less bottom water oxygenation compared to 2018 and 2019 due to increased stratification; SST in BB was found to be increasing at a rate of 0.11 ± 0.02 °C/year. Climate control on water column stratification are discussed and numerical experiments are used to compare the effects of different water column mixing scenarios on bottom water oxygenation.

Description: Dissolved silicate (H4SiO4) is essential for the formation of the opaline skeletal structures of diatoms and other siliceous plankton. A fraction of particulate biogenic silica (bSi) formed in surface waters sinks to the seabed, where it either dissolves and returns to the water column or is permanently buried. Global silica budgets are still poorly constrained since data on benthic bSi cycling are lacking, especially on continental margins. This study describes benthic bSi cycling in the Skagerrak, a sedimentary depocenter for particles from the North Sea. Biogenic silica burial fluxes, benthic H4SiO4 fluxes to the water column and bSi burial efficiencies are reported for nine stations by evaluating data from in-situ benthic landers and sediment cores with a diagenetic reaction-transport model. The model simulates bSi contents and H4SiO4 concentrations at all sites using a novel power law to describe bSi dissolution kinetics with a small number of adjustable parameters. Our results show that, on average, 1100 mmol m-2 yr-1 of bSi rains down to the Skagerrak basin seafloor, of which 50% is released back to overlying waters, with the remainder being buried. Biogenic silica cycling in the Skagerrak is generally consistent with previously reported global trends, showing higher Si fluxes and burial efficiencies than deep-sea sites and similar values compared to other continental margins. A significant finding of this work is a molar bSi-to-organic carbon burial ratio of 0.22 in Skagerrak sediments, which is distinctively lower compared to other continental margins. We suggest that the continuous dissolution of bSi in suspended sediments transported over long distances from the North Sea leads to the apparent decoupling between bSi and organic carbon in Skagerrak sediments.

Description: The uptake of dissolved oxygen from the atmosphere via air-sea gas exchange and its physical transport away from the region of uptake are crucial for supplying oxygen to the deep ocean. This process takes place in a few key regions that feature intense oxygen uptake, deep water formation, and physical oxygen export. In this study we analyze one such region, the Labrador Sea, utilizing the World Ocean Database (WOD) to construct a 65–year oxygen content time series in the Labrador Sea Water (LSW) layer (0–2200 m). The data reveal decadal variability associated with the strength of deep convection, with a maximum anomaly of 27 mol m–2 in 1992. There is no long-term trend in the time series, suggesting that the mean oxygen uptake is balanced by oxygen export out of the region. We compared the time series with output from nine models of the Ocean Model Intercomparison Project phase 1 in the Climate Model Intercomparison Project phase 6, (CMIP6-OMIP1), and constructed a “model score” to evaluate how well they match oxygen observations. Most CMIP6-OMIP1 models score around 50/100 points and the highest score is 57/100 for the ensemble mean, suggesting that improvements are needed. All of the models underestimate the maximum oxygen content anomaly in the 1990s. One possible cause for this is the representation of air-sea gas exchange for oxygen, with all models underestimating the mean uptake by a factor of two or more. Unrealistically deep convection and biased mean oxygen profiles may also contribute to the mismatch. Refining the representation of these processes in climate models could be vital for enhanced predictions of deoxygenation. In the CMIP6-OMIP1 multi-model mean, oxygen uptake has its maximum in 1980–1992, followed by a decrease in 1994–2006. There is a concurrent decrease in export, but oxygen storage also changes between the two periods, with oxygen accumulated in the first period and drained out in the second. Consequently, the change in oxygen export (5%) is much less than that in uptake (28%), suggesting that newly ventilated LSW which remains in the formation region acts to buffer the linkage between air-sea gas exchange and oxygen export.

Description: Ocean data synthesis products for specific biogeochemical essential ocean variables have the potential to facilitate today’s biogeochemical ocean data usage and comply with the Findable Accessible Interoperable and Reusable (FAIR) data principles. The products constitute key outputs from the Global Ocean Observation System, laying the observational foundation for information and services regarding climate and environmental status of the ocean. Using the Framework of Ocean Observing (FOO) readiness level concept, we present an evaluation framework for biogeochemical data synthesis products, which enables a systematic assessment of each product’s maturity. A new criteria catalog provides the foundation for assigning scores to the nine FOO readiness levels. As an example, we apply the assessment to four existing biogeochemical essential ocean variables data products. In descending readiness level order these are: The Surface Ocean CO2 Atlas (SOCAT); the Global Ocean Data Analysis Project (GLODAP); the MarinE MethanE and NiTrous Oxide (MEMENTO) data product and the Global Ocean Oxygen Database and ATlas (GO2DAT). Recognizing that the importance of adequate and comprehensive data from the essential ocean variables will grow, we recommend using this assessment framework to guide the biogeochemical data synthesis activities in their development. Moreover, we envision an overarching cross-platform FAIR biogeochemical data management system that sustainably supports the products individually and creates an integrated biogeochemical essential ocean variables data synthesis product; in short a system that provides truly comparable and FAIR data of the entire biogeochemical essential ocean variables spectrum.

Description: Enhanced mineral dissolution in the benthic environment is currently discussed as a potential technique for ocean alkalinity enhancement (OAE) to reduce atmospheric CO 2 levels. This study explores how biogeochemical processes affect the dissolution of alkaline minerals in surface sediments during laboratory incubation experiments. These involved introducing dunite and calcite to organic-rich sediments from the Baltic Sea under controlled conditions in an oxic environment. The sediment cores were incubated with Baltic Sea bottom water. Findings reveal that the addition of calcite increased the benthic alkalinity release from 0.4 μmol cm −2 d −1 (control) to 1.4 μmol cm −2 d −1 (calcite) as well as other weathering products such as calcium. However, these enhanced fluxes returned to lower fluxes after approximately 4 weeks yet still higher than the un-amended controls. Microbial activity appeared to be the primary driver for lowering pore water pH and thus enhanced weathering. In several sediment cores, pH profiles taken at the start of the experiments indicated activity of sulfur oxidizing Beggiatoa spp, which was verified by RNA-profiling of 16S rRNA genes. The pH profiles transitioned to those commonly associated with the activity of cable bacteria as the experiments progressed. The metabolic activity of cable bacteria would explain the significantly lower pH values (~5.6) at sediment depths of 1–3 cm, which would favor substantial calcite dissolution. However, a high abundance of cable bacteria was not reflected in 16S rRNA sequence data. Total alkalinity (TA) fluxes in these cores increased by a factor of ~3, with excess TA/calcium ratios indicating that the enhanced flux originated from calcite dissolution. The dissolution of dunite or the potential formation of secondary minerals could not be identified due to the strong natural flux of silicic acid, likely due to biogenic silica dissolution. Furthermore, no accumulation of potentially harmful metals such as nickel was observed, as highlighted as a potential risk in other studies concerning OAE. Given the complexity of sediment chemistry and changes of the benthic conditions induced by the incubation, it remains challenging to distinguish between natural and enhanced mineral weathering. Further investigation, including the identification of suitable tracers for mineral dissolution, are necessary to assess the feasibility of benthic weathering as a practical approach for OAE and climate change mitigation.