skip to main content


This content will become publicly available on September 22, 2024

Title: The competition between anthropogenic aerosol and greenhouse gas climate forcing is revealed by North Pacific water-mass changes

Modeled water-mass changes in the North Pacific thermocline, both in the subsurface and at the surface, reveal the impact of the competition between anthropogenic aerosols (AAs) and greenhouse gases (GHGs) over the past 6 decades. The AA effect overwhelms the GHG effect during 1950–1985 in driving salinity changes on density surfaces, while after 1985 the GHG effect dominates. These subsurface water-mass changes are traced back to changes at the surface, of which ~70% stems from the migration of density surface outcrops, equatorward due to regional cooling by AAs and subsequent poleward due to warming by GHGs. Ocean subduction connects these surface outcrop changes to the main thermocline. Both observations and models reveal this transition in climate forcing around 1985 and highlight the important role of AA climate forcing on our oceans’ water masses.

 
more » « less
Award ID(s):
2048336
NSF-PAR ID:
10494211
Author(s) / Creator(s):
; ; ; ;
Publisher / Repository:
American Association for the Advancement of Science
Date Published:
Journal Name:
Science Advances
Volume:
9
Issue:
38
ISSN:
2375-2548
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Unlike greenhouse gases (GHGs), anthropogenic aerosol (AA) concentrations have increased and then decreased over the past century or so, with the timing of the peak concentration varying in different regions. To date, it has been challenging to separate the climate impact of AAs from that due to GHGs and background internal variability. We use a pattern recognition method, taking advantage of spatiotemporal covariance information, to isolate the forced patterns for the surface ocean and associated atmospheric variables from the all-but-one forcing Community Earth System Model ensembles. We find that the aerosol-forced responses are dominated by two leading modes, with one associated with the historical increase and future decrease of global mean aerosol concentrations (dominated by the Northern Hemisphere sources) and the other due to the transition of the primary sources of AA from the west to the east and also from Northern Hemisphere extratropical regions to tropical regions. In particular, the aerosol transition effect, to some extent compensating the global mean effect, exhibits a zonal asymmetry in the surface temperature and salinity responses. We also show that this transition effect dominates the total AA effect during recent decades, e.g., 1967–2007.

     
    more » « less
  2. Abstract

    During recent decades, both greenhouse gases (GHGs) and anthropogenic aerosols (AAs) drove major changes in the Earth's energy imbalance. However, their respective fingerprints in changes to ocean heat content (OHC) have been difficult to isolate and detect when global or hemispheric averages are used. Based on a pattern recognition analysis, we show that AAs drive an interhemispheric asymmetry within the 20°‐35° latitude band in historical OHC change due to the southward shift of the atmospheric and ocean circulation system. This forced pattern is distinct from the GHG‐induced pattern, which dominates the asymmetry in higher latitudes. Moreover, it is found that this significant aerosol‐forced OHC trend pattern can only be captured in analyzed periods of 20 years or longer and including 1975–1990. Using these distinct spatiotemporal characteristics, we show that the fingerprint of aerosol climate forcing in ocean observations can be distinguished from both the stronger GHG‐induced signals and internal variability.

     
    more » « less
  3. null (Ed.)
    Abstract. Equilibrium climate sensitivity (ECS) has been directly estimated using reconstructions of past climates that are different than today's. A challenge to this approach is that temperature proxies integrate over the timescales of the fast feedback processes (e.g., changes in water vapor, snow, and clouds) that are captured in ECS as well as the slower feedback processes (e.g., changes in ice sheets and ocean circulation) that are not. A way around this issue is to treat the slow feedbacks as climate forcings and independently account for their impact on global temperature. Here we conduct a suite of Last Glacial Maximum (LGM) simulations using the Community Earth System Model version 1.2 (CESM1.2) to quantify the forcingand efficacy of land ice sheets (LISs) and greenhouse gases (GHGs) in order to estimate ECS. Our forcing and efficacy quantification adopts the effective radiative forcing (ERF) and adjustment framework and provides a complete accounting for the radiative, topographic, and dynamical impacts of LIS on surface temperatures. ERF and efficacy of LGM LIS are −3.2 W m−2 and 1.1, respectively. The larger-than-unity efficacy is caused by the temperature changes over land and the Northern Hemisphere subtropical oceans which are relatively larger than those in response to a doubling of atmospheric CO2. The subtropical sea-surface temperature (SST) response is linked to LIS-induced wind changes and feedbacks in ocean–atmosphere coupling and clouds. ERF and efficacy of LGM GHG are −2.8 W m−2 and 0.9, respectively. The lower efficacy is primarily attributed to a smaller cloud feedback at colder temperatures. Our simulations further demonstrate that the direct ECS calculation using the forcing, efficacy, and temperature response in CESM1.2 overestimates the true value in the model by approximately 25 % due to the neglect of slow ocean dynamical feedback. This is supported by the greater cooling (6.8 ∘C) in a fully coupled LGM simulation than that (5.3 ∘C) in a slab ocean model simulation with ocean dynamics disabled. The majority (67 %) of the ocean dynamical feedback is attributed to dynamical changes in the Southern Ocean, where interactions between upper-ocean stratification, heat transport, and sea-ice cover are found to amplify the LGM cooling. Our study demonstrates the value of climate models in the quantification of climate forcings and the ocean dynamical feedback, which is necessary for an accurate direct ECS estimation. 
    more » « less
  4. Abstract

    Atmospheric CO2 and anthropogenic aerosols (AA) have increased simultaneously. Because of their opposite radiative effects, these increases may offset each other, which may lead to some nonlinear effects. Here the seasonal and regional characteristics of this nonlinear effect from the CO2 and AA forcings are investigated using the fully coupled Community Earth System Model. Results show that nonlinear effects are small in the global mean of the top-of-the-atmosphere radiative fluxes, surface air temperature, and precipitation. However, significant nonlinear effects exist over the Arctic and other extratropical regions during certain seasons. When both forcings are included, Arctic sea ice in September–November decreases less than the linear combination of the responses to the individual forcings due to a higher sea ice sensitivity to the CO2-induced warming than the sensitivity to the AA-induced cooling. This leads to less Arctic warming in the combined-forcing experiment due to reduced energy release from the Arctic Ocean to the atmosphere. Some nonlinear effects on precipitation in June–August are found over East Asia, with the northward-shifted East Asian summer rain belt to oppose the CO2 effect. In December–February, the aerosol loading over Europe in the combined-forcing experiment is higher than that due to the AA forcing, resulting from CO2-induced circulation changes. The changed aerosol loading results in regional thermal responses due to aerosol direct and indirect effects, weakening the combined changes of temperature and circulation. This study highlights the need to consider nonlinear effects from historical CO2 and AA forcings in seasonal and regional climate attribution analyses.

     
    more » « less
  5. Boreal lakes are the most abundant lakes on Earth. Changes in acid rain deposition, climate, and catchment land use have increased lateral fluxes of terrestrial dissolved organic matter (DOM), resulting in a widespread browning of boreal freshwaters. This browning affects the aqueous communities and ecosystem processes, and boost emissions of the greenhouse gases (GHG) CH 4 , CO 2 , and N 2 O. In this study, we predicted biotic saturation of GHGs in boreal lakes by using a set of chemical, hydrological, climate, and land use parameters. For this purpose, concentrations of GHGs and nutrients (organic C, -P, and -N) were determined in surface water samples from 73 lakes in south-eastern Norway covering wide ranges in DOM and nutrient concentrations, as well as catchment properties and land use. The spatial variation in saturation of each GHG is related to explanatory variables. Catchment characteristics (hydrological and climate parameters) such as lake size and summer precipitation, as well as NDVI, were key determinants when fitting GAM models for CH 4 and CO 2 saturation (explaining 71 and 54%, respectively), while summer precipitation and land use data were the best predictors for the N 2 O saturation, explaining almost 50% of deviance. Our results suggest that lake size, precipitation, and terrestrial primary production in the watershed control the saturation of GHG in boreal lakes. These predictions based on the 73-lake dataset was validated against an independent dataset from 46 lakes in the same region. Together, this provides an improved understanding of drivers and spatial variation in GHG saturation in boreal lakes across wide gradients of lake and catchment properties. The assessment highlights the need to incorporate multiple explanatory parameters in prediction models of GHGs for extrapolation across the boreal biome. 
    more » « less