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Abstract This study characterized ocean biological carbon pump metrics in the second iteration of the REgional Carbon Cycle Assessment and Processes (RECCAP2) project. The analysis here focused on comparisons of global and biome‐scale regional patterns in particulate organic carbon (POC) production and sinking flux from the RECCAP2 ocean biogeochemical model ensemble against observational products derived from satellite remote sensing, sediment traps, and geochemical methods. There was generally good model‐data agreement in mean large‐scale spatial patterns, but with substantial spread across the model ensemble and observational products. The global‐integrated, model ensemble‐mean export production, taken as the sinking POC flux at 100 m (6.08 ± 1.17 Pg C yr⁻¹), and export ratio defined as sinking flux divided by net primary production (0.154 ± 0.026) both fell at the lower end of observational estimates. Comparison with observational constraints also suggested that the model ensemble may have underestimated regional biological CO₂drawdown and air‐sea CO₂flux in high productivity regions. Reasonable model‐data agreement was found for global‐integrated, ensemble‐mean sinking POC flux into the deep ocean at 1,000 m (0.65 ± 0.24 Pg C yr⁻¹) and the transfer efficiency defined as flux at 1,000 m divided by flux at 100 m (0.122 ± 0.041), with both variables exhibiting considerable regional variability. The RECCAP2 analysis presents standard ocean biological carbon pump metrics for assessing biogeochemical model skill, metrics that are crucial for further modeling efforts to resolve remaining uncertainties involving system‐level interactions between ocean physics and biogeochemistry. 

Abstract The ocean is a major carbon sink and takes up 25%–30% of the anthropogenically emitted CO₂. A state‐of‐the‐art method to quantify this sink are global ocean biogeochemistry models (GOBMs), but their simulated CO₂uptake differs between models and is systematically lower than estimates based on statistical methods using surface oceanpCO₂and interior ocean measurements. Here, we provide an in‐depth evaluation of ocean carbon sink estimates from 1980 to 2018 from a GOBM ensemble. As sources of inter‐model differences and ensemble‐mean biases our study identifies (a) the model setup, such as the length of the spin‐up, the starting date of the simulation, and carbon fluxes from rivers and into sediments, (b) the simulated ocean circulation, such as Atlantic Meridional Overturning Circulation and Southern Ocean mode and intermediate water formation, and (c) the simulated oceanic buffer capacity. Our analysis suggests that a late starting date and biases in the ocean circulation cause a too low anthropogenic CO₂uptake across the GOBM ensemble. Surface ocean biogeochemistry biases might also cause simulated anthropogenic fluxes to be too low, but the current setup prevents a robust assessment. For simulations of the ocean carbon sink, we recommend in the short‐term to (a) start simulations at a common date before the industrialization and the associated atmospheric CO₂increase, (b) conduct a sufficiently long spin‐up such that the GOBMs reach steady‐state, and (c) provide key metrics for circulation, biogeochemistry, and the land‐ocean interface. In the long‐term, we recommend improving the representation of these metrics in the GOBMs. 

The interplay between ocean circulation and coral metabolism creates highly variable biogeochemical conditions in space and time across tropical coral reefs. Yet, relatively little is known quantitatively about the spatiotemporal structure of these variations. To address this gap, we use the Coupled Ocean Atmosphere Wave and Sediment Transport (COAWST) model, to which we added the Biogeochemical Elemental Cycling (BEC) model computing the biogeochemical processes in the water column, and a coral polyp physiology module that interactively simulates coral photosynthesis, respiration and calcification. The coupled model, configured for the north-shore of Moorea Island, successfully simulates the observed (i) circulation across the wave regimes, (ii) magnitude of the metabolic rates, and (iii) large gradients in biogeochemical conditions across the reef. Owing to the interaction between coral net community production (NCP) and coral calcification, the model simulates distinct day versus night gradients, especially for pH and the saturation state of seawater with respect to aragonite (Ω_α). The strength of the gradients depends non-linearly on the wave regime and the resulting residence time of water over the reef with the low wave regime creating conditions that are considered as “extremely marginal” for corals. With the average water parcel passing more than twice over the reef, recirculation contributes further to the accumulation of these metabolic signals. We find diverging temporal and spatial relationships between total alkalinity (TA) and dissolved inorganic carbon (DIC) (≈ 0.16 for the temporal vs. ≈ 1.8 for the spatial relationship), indicating the importance of scale of analysis for this metric. Distinct biogeochemical niches emerge from the simulated variability, i.e., regions where the mean and variance of the conditions are considerably different from each other. Such biogeochemical niches might cause large differences in the exposure of individual corals to the stresses associated with e.g., ocean acidification. At the same time, corals living in the different biogeochemical niches might have adapted to the differing conditions, making the reef, perhaps, more resilient to change. Thus, a better understanding of the mosaic of conditions in a coral reef might be useful to assess the health of a coral reef and to develop improved management strategies. 

Abstract We assess the Southern Ocean CO₂uptake (1985–2018) using data sets gathered in the REgional Carbon Cycle Assessment and Processes Project Phase 2. The Southern Ocean acted as a sink for CO₂with close agreement between simulation results from global ocean biogeochemistry models (GOBMs, 0.75 ± 0.28 PgC yr⁻¹) andpCO₂‐observation‐based products (0.73 ± 0.07 PgC yr⁻¹). This sink is only half that reported by RECCAP1 for the same region and timeframe. The present‐day net uptake is to first order a response to rising atmospheric CO₂, driving large amounts of anthropogenic CO₂(C_ant) into the ocean, thereby overcompensating the loss of natural CO₂to the atmosphere. An apparent knowledge gap is the increase of the sink since 2000, withpCO₂‐products suggesting a growth that is more than twice as strong and uncertain as that of GOBMs (0.26 ± 0.06 and 0.11 ± 0.03 Pg C yr⁻¹ decade⁻¹, respectively). This is despite nearly identicalpCO₂trends in GOBMs andpCO₂‐products when both products are compared only at the locations wherepCO₂was measured. Seasonal analyses revealed agreement in driving processes in winter with uncertainty in the magnitude of outgassing, whereas discrepancies are more fundamental in summer, when GOBMs exhibit difficulties in simulating the effects of the non‐thermal processes of biology and mixing/circulation. Ocean interior accumulation of C_antpoints to an underestimate of C_antuptake and storage in GOBMs. Future work needs to link surface fluxes and interior ocean transport, build long overdue systematic observation networks and push toward better process understanding of drivers of the carbon cycle. 

Abstract. As the largest active carbon reservoir on Earth, the ocean is a cornerstone of the global carbon cycle, playing a pivotal role in modulating ocean health and regulating climate. Understanding these crucial roles requires access to a broad array of data products documenting the changing chemistry of the global ocean as a vast and interconnected system. This review article provides a comprehensive overview of 60 existing ocean carbonate chemistry data products, encompassing compilations of cruise datasets, derived gap-filled data products, model simulations, and compilations thereof. It is intended to help researchers identify and access data products that best align with their research objectives, thereby advancing our understanding of the ocean's evolving carbonate chemistry. 

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. 

Abstract. Accurate assessment of anthropogenic carbon dioxide (CO2) emissions and their redistribution among the atmosphere, ocean, and terrestrial biosphere in a changing climate is critical to better understand the global carbon cycle, support the development of climate policies, and project future climate change. Here we describe and synthesize datasets and methodologies to quantify the five major components of the global carbon budget and their uncertainties. Fossil CO2 emissions (EFOS) are based on energy statistics and cement production data, while emissions from land-use change (ELUC) are based on land-use and land-use change data and bookkeeping models. Atmospheric CO2 concentration is measured directly, and its growth rate (GATM) is computed from the annual changes in concentration. The global net uptake of CO2 by the ocean (SOCEAN, called the ocean sink) is estimated with global ocean biogeochemistry models and observation-based fCO2 products (fCO2 is the fugacity of CO2). The global net uptake of CO2 by the land (SLAND, called the land sink) is estimated with dynamic global vegetation models. Additional lines of evidence on land and ocean sinks are provided by atmospheric inversions, atmospheric oxygen measurements, and Earth system models. The sum of all sources and sinks results in the carbon budget imbalance (BIM), a measure of imperfect data and incomplete understanding of the contemporary carbon cycle. All uncertainties are reported as ±1σ. For the year 2023, EFOS increased by 1.3 % relative to 2022, with fossil emissions at 10.1 ± 0.5 GtC yr−1 (10.3 ± 0.5 GtC yr−1 when the cement carbonation sink is not included), and ELUC was 1.0 ± 0.7 GtC yr−1, for a total anthropogenic CO2 emission (including the cement carbonation sink) of 11.1 ± 0.9 GtC yr−1 (40.6 ± 3.2 GtCO2 yr−1). Also, for 2023, GATM was 5.9 ± 0.2 GtC yr−1 (2.79 ± 0.1 ppm yr−1; ppm denotes parts per million), SOCEAN was 2.9 ± 0.4 GtC yr−1, and SLAND was 2.3 ± 1.0 GtC yr−1, with a near-zero BIM (−0.02 GtC yr−1). The global atmospheric CO2 concentration averaged over 2023 reached 419.31 ± 0.1 ppm. Preliminary data for 2024 suggest an increase in EFOS relative to 2023 of +0.8 % (−0.2 % to 1.7 %) globally and an atmospheric CO2 concentration increase by 2.87 ppm, reaching 422.45 ppm, 52 % above the pre-industrial level (around 278 ppm in 1750). Overall, the mean of and trend in the components of the global carbon budget are consistently estimated over the period 1959–2023, with a near-zero overall budget imbalance, although discrepancies of up to around 1 GtC yr−1 persist for the representation of annual to semi-decadal variability in CO2 fluxes. Comparison of estimates from multiple approaches and observations shows the following: (1) a persistent large uncertainty in the estimate of land-use change emissions, (2) low agreement between the different methods on the magnitude of the land CO2 flux in the northern extra-tropics, and (3) a discrepancy between the different methods on the mean ocean sink. This living-data update documents changes in methods and datasets applied to this most recent global carbon budget as well as evolving community understanding of the global carbon cycle. The data presented in this work are available at https://doi.org/10.18160/GCP-2024 (Friedlingstein et al., 2024).