ALBERT

Description: The presented pilot for the Synthesis Product for Ocean Time Series (SPOTS) includes data from 12 fixed ship-based time-series programs. The related stations represent unique open-ocean and coastal marine environments within the Atlantic Ocean, Pacific Ocean, Mediterranean Sea, Nordic Seas, and Caribbean Sea. The focus of the pilot has been placed on biogeochemical essential ocean variables: dissolved oxygen, dissolved inorganic nutrients, inorganic carbon (pH, total alkalinity, dissolved inorganic carbon, and partial pressure of CO2), particulate matter, and dissolved organic carbon. The time series used include a variety of temporal res- olutions (monthly, seasonal, or irregular), time ranges (10–36 years), and bottom depths (80–6000 m), with the oldest samples dating back to 1983 and the most recent one corresponding to 2021. Besides having been harmo- nized into the same format (semantics, ancillary data, units), the data were subjected to a qualitative assessment in which the applied methods were evaluated and categorized. The most recently applied methods of the time- series programs usually follow the recommendations outlined by the Bermuda Time Series Workshop report (Lorenzoni and Benway, 2013), which is used as the main reference for “method recommendations by prevalent initiatives in the field”. However, measurements of dissolved oxygen and pH, in particular, still show room for improvement. Additional data quality descriptors include precision and accuracy estimates, indicators for data variability, and offsets compared to a reference and widely recognized data product for the global ocean: the GLobal Ocean Data Analysis Project (GLODAP). Generally, these descriptors indicate a high level of continuity in measurement quality within time-series programs and a good consistency with the GLODAP data product, even though robust comparisons to the latter are limited. The data are available as (i) a merged comma-separated file that is compliant with the World Ocean Circulation Experiment (WOCE) exchange format and (ii) a format dependent on user queries via the Environmental Research Division’s Data Access Program (ERDDAP) server of the Global Ocean Observing System (GOOS). The pilot increases the data utility, findability, accessibility, interoperability, and reusability following the FAIR philosophy, enhancing the readiness of biogeochemical time series. It facilitates a variety of applications that benefit from the collective value of biogeochemical time-series observations and forms the basis for a sustained time-series living data product, SPOTS, complementing relevant products for the global interior ocean carbon data (GLobal Ocean Data Analysis Project), global surface ocean carbon data (Surface Ocean CO2 Atlas; SOCAT), and global interior and surface methane and nitrous oxide data (MarinE MethanE and NiTrous Oxide product). Aside from the actual data compilation, the pilot project produced suggestions for reporting metadata, im- plementing quality control measures, and making estimations about uncertainty. These recommendations aim to encourage the community to adopt more consistent and uniform practices for analysis and reporting and to update these practices regularly. The detailed recommendations, links to the original time-series programs, the original data, their documentation, and related efforts are available on the SPOTS website. This site also pro- vides access to the data product (DOI: https://doi.org/10.26008/1912/bco-dmo.896862.2, Lange et al., 2024) and ancillary data.

Description: Marine particles of different nature are found throughout the global ocean. The term "marine particles" describes detritus aggregates and fecal pellets as well as bacterioplankton, phytoplankton, zooplankton and nekton. Here, we present a global particle size distribution dataset obtained with several Underwater Vision Profiler 5 (UVP5) camera systems. Overall, within the 64 mu m to about 50 mm size range covered by the UVP5, detrital particles are the most abundant component of all marine particles; thus, measurements of the particle size distribution with the UVP5 can yield important information on detrital particle dynamics. During deployment, which is possible down to 6000 m depth, the UVP5 images a volume of about 1 L at a frequency of 6 to 20 Hz. Each image is segmented in real time, and size measurements of particles are automatically stored. All UVP5 units used to generate the dataset presented here were inter-calibrated using a UVP5 high-definition unit as reference. Our consistent particle size distribution dataset contains 8805 vertical profiles collected between 19 June 2008 and 23 November 2020. All major ocean basins, as well as the Mediterranean Sea and the Baltic Sea, were sampled. A total of 19 % of all profiles had a maximum sampling depth shallower than 200 dbar, 38 % sampled at least the upper 1000 dbar depth range and 11 % went down to at least 3000 dbar depth. First analysis of the particle size distribution dataset shows that particle abundance is found to be high at high latitudes and in coastal areas where surface productivity or continental inputs are elevated. The lowest values are found in the deep ocean and in the oceanic gyres. Our dataset should be valuable for more in-depth studies that focus on the analysis of regional, temporal and global patterns of particle size distribution and flux as well as for the development and adjustment of regional and global biogeochemical models. The marine particle size distribution dataset (Kiko et al., 2021) is available at https://doi.org/10.1594/PANGAEA.924375.

Description: Changes in stratospheric ozone concentrations and increasing concentrations of greenhouse gases (GHGs) alter the temperature structure of the atmosphere and drive changes in the atmospheric and oceanic circulation. We systematically investigate the impacts of ozone recovery and increasing GHGs on the atmospheric and oceanic circulation in the Southern Hemisphere during the twenty-first century using a unique coupled ocean–atmosphere climate model with interactive ozone chemistry and enhanced oceanic resolution. We use the high-emission scenario SSP5-8.5 for GHGs under which the springtime Antarctic total column ozone returns to 1980s levels by 2048 in our model, warming the lower stratosphere and strengthening the stratospheric westerly winds. We perform a spatial analysis and show for the first time that the austral spring stratospheric response to GHGs exhibits a marked planetary wavenumber 1 (PW1) pattern, which reinforces the response to ozone recovery over the Western Hemisphere and weakens it over the Eastern Hemisphere. These changes, which imply an eastward phase shift in the PW1, largely cancel out in the zonal mean. The Southern Hemisphere residual circulation strengthens during most of the year due to the increase in GHGs and weakens in spring due to ozone recovery. However, we find that in November the GHGs also drive a weakening of the residual circulation, reinforcing the effect of ozone recovery, which represents another novel result. At the surface, the westerly winds weaken and shift equatorward due to ozone recovery, driving a weak decrease in the transport of the Antarctic Circumpolar Current and in the Agulhas leakage and a cooling of the upper ocean, which is most pronounced in the latitudinal band 35–45∘ S. The increasing GHGs drive changes in the opposite direction that overwhelm the ozone effect. The total changes at the surface and in the oceanic circulation are nevertheless weaker in the presence of ozone recovery than those induced by GHGs alone, highlighting the importance of the Montreal Protocol in mitigating some of the impacts of climate change. We additionally compare the combined effect of interactively calculated ozone recovery and increasing GHGs with their combined effect in an ensemble in which we prescribe the CMIP6 ozone field. This second ensemble simulates a weaker ozone effect in all the examined fields, consistent with its weaker increase in ozone. The magnitude of the difference between the simulated changes at the surface and in the oceanic circulation in the two ensembles is as large as the ozone effect itself. This shows the large uncertainty that is associated with the choice of the ozone field and how the ozone is treated.

Description: Nitrogen (N) is a crucial limiting nutrient for phytoplankton growth in the ocean. The main source of bioavailable N in the ocean is delivered by N2-fixing diazotrophs in the surface layer. Since field observation of N2 fixation are spatially and temporally sparse, the fundamental processes and mechanisms controlling N2 fixation are not well understood and constrained. Here, we implement benthic denitrification in an Earth System Model of intermediate complexity (UVic-ESCM 2.9) coupled to an optimality-based plankton ecosystem model (OPEM v1.1). Benthic denitrification occurs mostly in coastal upwelling regions and on shallow continental shelves, and is the largest N-loss process in the global ocean. We calibrate our model against three different combinations of observed Chl, NO3-, PO43-, O2 and N* = NO3- −16PO43- +2.9. The inclusion of N* provides a powerful constraint on biogeochemical model behavior. Our new model version including benthic denitrification simulates higher global rates of N2 fixation with a more realistic distribution extending to higher latitudes that are supported by independent estimates based on geochemical data. Oxygen deficient zone volume and water column denitrification rates are reduced in the new version, indicating that including benthic denitrification may improve global biogeochemical models that commonly overestimate anoxic zones. With the improved representation of the ocean N cycle, our new model configuration also yields better global net primary production (NPP) when compared to the independent datasets not included in the calibration. Benthic denitrification plays an important role shaping N2 fixation and NPP throughout the global ocean in our model, and should be considered when evaluating and predicting their response to environmental change.

Description: Since a pH sensor has become available that is principally suitable for use on demanding autonomous measurement platforms, the marine CO2 system can be observed independently and continuously by Biogeochemical Argo floats. This opens the potential to detect variability and long-term changes in interior ocean inorganic carbon storage and quantify the ocean sink for atmospheric CO2. In combination with a second parameter of the marine CO2 system, pH can be a useful tool to derive the surface ocean CO2 partial pressure (pCO2). The large spatiotemporal variability in the marine CO2 system requires sustained observations to decipher trends and study the impacts of short-term events (e.g., eddies, storms, phytoplankton blooms) but also puts a high emphasis on the quality control of float-based pH measurements. In consequence, a consistent and rigorous quality control procedure is being established to correct sensor offsets or drifts as the interpretation of changes depends on accurate data. By applying current standardized routines of the Argo data management to pH measurements from a pH / O2 float pilot array in the subpolar North Atlantic Ocean, we assess the uncertainties and lack of objective criteria associated with the standardized routines, notably the choice of the reference method for the pH correction (CANYON-B, LIR-pH, ESPER-NN, and ESPER-LIR) and the reference depth for this adjustment. For the studied float array, significant differences ranging between ca. 0.003 pH units and ca. 0.04 pH units are observed between the four reference methods which have been proposed to correct float pH data. Through comparison against discrete and underway pH data from other platforms, an assessment of the adjusted float pH data quality is presented. The results point out noticeable discrepancies near the surface of 〉 0.004 pH units. In the context of converting surface ocean pH measurements into pCO2 data for the purpose of deriving air–sea CO2 fluxes, we conclude that an accuracy requirement of 0.01 pH units (equivalent to a pCO2 accuracy of 10 µatm as a minimum requirement for potential future inclusion in the Surface Ocean CO2 Atlas, SOCAT, database) is not systematically achieved in the upper ocean. While the limited dataset and regional focus of our study do not allow for firm conclusions, the evidence presented still calls for the inclusion of an additional independent pH reference in the surface ocean in the quality control routines. We therefore propose a way forward to enhance the float pH quality control procedure. In our analysis, the current philosophy of pH data correction against climatological reference data at one single depth in the deep ocean appears insufficient to assure adequate data quality in the surface ocean. Ideally, an additional reference point should be taken at or near the surface where the resulting pCO2 data are of the highest importance to monitor the air–sea exchange of CO2 and would have the potential to very significantly augment the impact of the current observation network.

Description: The climate science community aims to improve our understanding of climate change due to anthropogenic influences on atmospheric composition and the Earth's surface. Yet not all climate interactions are fully understood and diversity in climate model experiments persists as assessed in the latest Intergovernmental Panel on Climate Change (IPCC) assessment report. This article synthesizes current challenges and emphasizes opportunities for advancing our understanding of climate change and model diversity. The perspective of this article is based on expert views from three multi-model intercomparison projects (MIPs) – the Precipitation Driver Response MIP (PDRMIP), the Aerosol and Chemistry MIP (AerChemMIP), and the Radiative Forcing MIP (RFMIP). While there are many shared interests and specialisms across the MIPs, they have their own scientific foci and specific approaches. The partial overlap between the MIPs proved useful for advancing the understanding of the perturbation-response paradigm through multi-model ensembles of Earth System Models of varying complexity. It specifically facilitated contributions to the research field through sharing knowledge on best practices for the design of model diagnostics and experimental strategies across MIP boundaries, e.g., for estimating effective radiative forcing. We discuss the challenges of gaining insights from highly complex models that have specific biases and provide guidance from our lessons learned. Promising ideas to overcome some long-standing challenges in the near future are kilometer-scale experiments to better simulate circulation-dependent processes where it is possible, and machine learning approaches for faster and better sub-grid scale parameterizations where they are needed. Both would improve our ability to adopt a smart experimental design with an optimal tradeoff between resolution, complexity and simulation length. Future experiments can be evaluated and improved with sophisticated methods that leverage multiple observational datasets, and thereby, help to advance the understanding of climate change and its impacts.

Description: Phytoplankton forms the base of the marine food web by transforming CO2 into organic carbon via photosynthesis. Some of the organic carbon is then transferred through the food web and exported into the deep ocean, a process known as the biological carbon pump. Despite the importance of phytoplankton for marine ecosystems and the global carbon cycle, projections of phytoplankton biomass in response to climate change differ strongly across Earth system models, illustrating uncertainty in our understanding of the underlying processes. Differences are especially large in the Southern Ocean, a region that is notoriously difficult to represent in models. Here, we argue that water column-integrated phytoplankton biomass in the Southern Ocean is projected to largely remain unchanged under climate change by the CMIP6 multi-model ensemble because of a shifting balance of bottom-up and top-down processes driven by a shoaling mixed layer depth. A shallower mixed layer is projected to improve growth conditions and consequently weaken bottom-up control. In addition to enhanced phytoplankton growth, the shoaling of the mixed layer also compresses phytoplankton closer to the surface and promotes zooplankton grazing efficiency, thus intensifying top-down control. Overall, our results suggest that while changes in bottom-up conditions stimulate enhanced growth, intensified top-down control opposes an increase in phytoplankton and becomes increasingly important for phytoplankton response under climate change in the Southern Ocean.

Description: We examine the impact of horizontal resolution and model time step on the climate of the OpenIFS version 43r3 atmospheric general circulation model. A series of simulations for the period 1979–2019 are conducted with various horizontal resolutions (i.e. ∼100, ∼50, and ∼25 km) while maintaining the same time step (i.e. 15 min) and using different time steps (i.e. 60, 30, and 15 min) at 100 km horizontal resolution. We find that the surface zonal wind bias is significantly reduced over certain regions such as the Southern Ocean and the Northern Hemisphere mid-latitudes and in tropical and subtropical regions at a high horizontal resolution (i.e. ∼25 km). Similar improvement is evident too when using a coarse-resolution model (∼100 km) with a smaller time step (i.e. 30 and 15 min). We also find improvements in Rossby wave amplitude and phase speed, as well as in weather regime patterns, when a smaller time step or higher horizontal resolution is used. The improvement in the wind bias when using the shorter time step is mostly due to an increase in shallow and mid-level convection that enhances vertical mixing in the lower troposphere. The enhanced mixing allows frictional effects to influence a deeper layer and reduces wind and wind speed throughout the troposphere. However, precipitation biases generally increase with higher horizontal resolutions or smaller time steps, whereas the surface air temperature bias exhibits a small improvement over North America and the eastern Eurasian continent. We argue that the bias improvement in the highest-horizontal-resolution (i.e. ∼25 km) configuration benefits from a combination of both the enhanced horizontal resolution and the shorter time step. In summary, we demonstrate that, by reducing the time step in the coarse-resolution (∼100 km) OpenIFS model, one can alleviate some climate biases at a lower cost than by increasing the horizontal resolution.

Description: Here we present a confocal Fe K-edge μ-XANES method (where XANES stands for X-ray absorption near-edge spectroscopy) for the analysis of Fe oxidation state in heterogeneous and one-side-polished samples. The new technique allows for an analysis of small volumes with high spatial 3D resolution of 〈100 µm3. The probed volume is restricted to that just beneath the surface of the exposed object. This protocol avoids contamination of the signal by the host material and minimizes self-absorption effects. This technique has been tested on a set of experimental glasses with a wide range of Fe3+  ΣFe ratios. The method was applied to the analysis of natural melt inclusions trapped in forsteritic to fayalitic olivine crystals of the Hekla volcano, Iceland. Our measurements reveal changes in Fe3+  ΣFe from 0.17 in basaltic up to 0.45 in dacitic melts, whereas the magnetite–ilmenite equilibrium shows redox conditions with Fe3+  ΣFe ≤0.20 (close to FMQ, fayalite–magnetite–quartz redox equilibrium) along the entire range of Hekla melt compositions. This discrepancy indicates that the oxidized nature of glasses in the melt inclusions could be related to the post-entrapment process of diffusive hydrogen loss from inclusions and associated oxidation of Fe in the melt. The Fe3+  ΣFe ratio in silicic melts is particularly susceptible to this process due to their low FeO content, and it should be critically evaluated before petrological interpretation.