Search for: All records

The notion of climate sensitivity has become synonymous with equilibrium climate sensitivity (ECS), or the equilibrium response of the Earth system to a doubling of CO₂. But there is a hierarchy of measures of climate sensitivity, which can be arranged in order of increasing complexity and societal relevance and which mirror the historical development of climate modeling. Elements of this hierarchy include the well-known ECS and transient climate response and the lesser-known transient climate response to cumulative emissions and zero emissions commitment. This article describes this hierarchy of climate sensitivities and associated modeling approaches. Key concepts reviewed along the way include climate forcing and feedback, ocean heat uptake, and the airborne fraction of cumulative emissions. We employ simplified theoretical models throughout to encapsulate well-understood aspects of these quantities and to highlight gaps in our understanding and areas for future progress.▪There is a hierarchy of measures of climate sensitivity, which exhibit a range of complexity and societal relevance.▪Equilibrium climate sensitivity is only one of these measures, and our understanding of it may have reached a plateau.▪The more complex measures introduce new quantities, such as ocean heat uptake coefficient and airborne fraction, which deserve increased attention. 

Ocean deoxygenation due to anthropogenic warming represents a major threat to marine ecosystems and fisheries. Challenges remain in simulating the modern observed changes in the dissolved oxygen (O₂). Here, we present an analysis of upper ocean (0-700m) deoxygenation in recent decades from a suite of the Coupled Model Intercomparison Project phase 6 (CMIP6) ocean biogeochemical simulations. The physics and biogeochemical simulations include both ocean-only (the Ocean Model Intercomparison Project Phase 1 and 2, OMIP1 and OMIP2) and coupled Earth system (CMIP6 Historical) configurations. We examine simulated changes in the O₂inventory and ocean heat content (OHC) over the past 5 decades across models. The models simulate spatially divergent evolution of O₂trends over the past 5 decades. The trend (multi-model mean and spread) for upper ocean global O₂inventory for each of the MIP simulations over the past 5 decades is 0.03 ± 0.39×1014 [mol/decade] for OMIP1, −0.37 ± 0.15×10¹⁴[mol/decade] for OMIP2, and −1.06 ± 0.68×10¹⁴[mol/decade] for CMIP6 Historical, respectively. The trend in the upper ocean global O₂inventory for the latest observations based on the World Ocean Database 2018 is −0.98×10¹⁴[mol/decade], in line with the CMIP6 Historical multi-model mean, though this recent observations-based trend estimate is weaker than previously reported trends. A comparison across ocean-only simulations from OMIP1 and OMIP2 suggests that differences in atmospheric forcing such as surface wind explain the simulated divergence across configurations in O₂inventory changes. Additionally, a comparison of coupled model simulations from the CMIP6 Historical configuration indicates that differences in background mean states due to differences in spin-up duration and equilibrium states result in substantial differences in the climate change response of O₂. Finally, we discuss gaps and uncertainties in both ocean biogeochemical simulations and observations and explore possible future coordinated ocean biogeochemistry simulations to fill in gaps and unravel the mechanisms controlling the O₂changes. 

Marine microbes form the base of ocean food webs and drive ocean biogeochemical cycling. Yet little is known about the ability of microbial populations to adapt as they are advected through changing conditions. Here, we investigated the interplay between physical and biological timescales using a model of adaptation and an eddy-resolving ocean circulation climate model. Two criteria were identified that relate the timing and nature of adaptation to the ratio of physical to biological timescales. Genetic adaptation was impeded in highly variable regimes by nongenetic modifications but was promoted in more stable environments. An evolutionary trade-off emerged where greater short-term nongenetic transgenerational effects (low-γ strategy) enabled rapid responses to environmental fluctuations but delayed genetic adaptation, while fewer short-term transgenerational effects (high-γ strategy) allowed faster genetic adaptation but inhibited short-term responses. Our results demonstrate that the selective pressures for organisms within a single water mass vary based on differences in generation timescales resulting in different evolutionary strategies being favored. Organisms that experience more variable environments should favor a low-γ strategy. Furthermore, faster cell division rates should be a key factor in genetic adaptation in a changing ocean. Understanding and quantifying the relationship between evolutionary and physical timescales is critical for robust predictions of future microbial dynamics. 

Abstract Numerical models of ocean biogeochemistry are relied upon to make projections about the impact of climate change on marine resources and test hypotheses regarding the drivers of past changes in climate and ecosystems. In large areas of the ocean, iron availability regulates the functioning of marine ecosystems and hence the ocean carbon cycle. Accordingly, our ability to quantify the drivers and impacts of fluctuations in ocean ecosystems and carbon cycling in space and time relies on first achieving an appropriate representation of the modern marine iron cycle in models. When the iron distributions from 13 global ocean biogeochemistry models are compared against the latest oceanic sections from the GEOTRACES program, we find that all models struggle to reproduce many aspects of the observed spatial patterns. Models that reflect the emerging evidence for multiple iron sources or subtleties of its internal cycling perform much better in capturing observed features than their simpler contemporaries, particularly in the ocean interior. We show that the substantial uncertainty in the input fluxes of iron results in a very wide range of residence times across models, which has implications for the response of ecosystems and global carbon cycling to perturbations. Given this large uncertainty, iron fertilization experiments based on any single current generation model should be interpreted with caution. Improvements to how such models represent iron scavenging and also biological cycling are needed to raise confidence in their projections of global biogeochemical change in the ocean. 

Abstract Anthropogenically forced changes in ocean biogeochemistry are underway and critical for the ocean carbon sink and marine habitat. Detecting such changes in ocean biogeochemistry will require quantification of the magnitude of the change (anthropogenic signal) and the natural variability inherent to the climate system (noise). Here we use Large Ensemble (LE) experiments from four Earth system models (ESMs) with multiple emissions scenarios to estimate Time of Emergence (ToE) and partition projection uncertainty for anthropogenic signals in five biogeochemically important upper‐ocean variables. We find ToEs are robust across ESMs for sea surface temperature and the invasion of anthropogenic carbon; emergence time scales are 20–30 yr. For the biological carbon pump, and sea surface chlorophyll and salinity, emergence time scales are longer (50+ yr), less robust across the ESMs, and more sensitive to the forcing scenario considered. We find internal variability uncertainty, and model differences in the internal variability uncertainty, can be consequential sources of uncertainty for projecting regional changes in ocean biogeochemistry over the coming decades. In combining structural, scenario, and internal variability uncertainty, this study represents the most comprehensive characterization of biogeochemical emergence time scales and uncertainty to date. Our findings delineate critical spatial and duration requirements for marine observing systems to robustly detect anthropogenic change. 

Abstract The air‐sea exchange of oxygen (O₂) is driven by changes in solubility, biological activity, and circulation. The total air‐sea exchange of O₂has been shown to be closely related to the air‐sea exchange of heat on seasonal timescales, with the ratio of the seasonal flux of O₂to heat varying with latitude, being higher in the extratropics and lower in the subtropics. This O₂/heat ratio is both a fundamental biogeochemical property of air‐sea exchange and a convenient metric for testing earth system models. Current estimates of the O₂/heat flux ratio rely on sparse observations of dissolved O₂, leaving it fairly unconstrained. From a model ensemble we show that the ratio of the seasonal amplitude of two atmospheric tracers, atmospheric potential oxygen (APO) and the argon‐to‐nitrogen ratio (Ar/O₂), exhibits a close relationship to the O₂/heat ratio of the extratropics (40–). The amplitude ratio,/, is relatively constant within the extratropics of each hemisphere due to the zonal mixing of the atmosphere./is not sensitive to atmospheric transport, as most of the observed spatial variability in the seasonal amplitude ofAPO is compensated by similar variations in(Ar/). From the relationship between/heat and/in the model ensemble, we determine that the atmospheric observations suggest hemispherically distinct/heat flux ratios of 3.30.3 and 4.70.8 nmolbetween 40 andin the Northern and Southern Hemispheres respectively, providing a useful constraint forand heat air‐sea fluxes in earth system models and observation‐based data products.