skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


Title: Interhemispheric Contrasts of Ocean Heat Content Change Reveals Distinct Fingerprints of Anthropogenic Climate Forcings
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
Award ID(s):
2048336
PAR ID:
10449975
Author(s) / Creator(s):
 ;  ;  ;  
Publisher / Repository:
DOI PREFIX: 10.1029
Date Published:
Journal Name:
Geophysical Research Letters
Volume:
50
Issue:
16
ISSN:
0094-8276
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; (, Journal of Climate)
    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. ; ; ; ; (, Geophysical Research Letters)
    Abstract Anthropogenic aerosols (AER) and greenhouse gases (GHG)—the leading drivers of the forced historical change—produce different large‐scale climate response patterns, with correlations trending from negative to positive over the past century. To understand what caused the time‐evolving comparison between GHG and AER response patterns, we apply a low‐frequency component analysis to historical surface ocean changes from CESM1 single‐forcing large‐ensemble simulations. While GHG response is characterized by its first leading mode, AER response consists of two distinct modes. The first one, featuring long‐term global AER increase and global cooling, opposes GHG response patterns up to the mid‐twentieth century. The second one, featuring multidecadal variations in AER distributions and interhemispheric asymmetric surface ocean changes, appears to reinforce the GHG warming effect over recent decades. AER thus can have both competing and synergistic effects with GHG as their emissions change temporally and spatially. 
    more » « less
  3. ; ; ; ; (, Science Advances)
    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
  4. ; ; ; ; ; ; (, Geophysical Research Letters)
    Abstract Ocean warming is a key factor impacting future changes in climate. Here we investigate vertical structure changes in globally averaged ocean heat content (OHC) in high‐ (HR) and low‐resolution (LR) future climate simulations with the Community Earth System Model (CESM). Compared with observation‐based estimates, the simulated OHC anomalies in the upper 700 and 2,000 m during 1960–2020 are more realistic in CESM‐HR than ‐LR. Under RCP8.5 scenario, the net surface heat into the ocean is very similar in CESM‐HR and ‐LR. However, CESM‐HR has a larger increase in OHC in the upper 250 m compared to CESM‐LR, but a smaller increase below 250 m. This difference can be traced to differences in eddy‐induced vertical heat transport between CESM‐HR and ‐LR in the historical period. Moreover, our results suggest that with the same heat input, upper‐ocean warming is likely to be underestimated by most non‐eddy‐resolving climate models. 
    more » « less
  5. ; ; ; ; ; ; (, npj Climate and Atmospheric Science)
    Abstract Arctic amplification (AA), the greater Arctic surface warming compared to the global average, has been widely attributed to increasing concentrations of greenhouse gases (GHG). However, less is known about the impacts of other forcings - notably, anthropogenic aerosols (AER) - and how they may compare to the impacts of GHG. Here we analyze sets of climate model simulations, specifically designed to isolate the AER and GHG effects on global climate. Surprisingly, we find stronger AA produced by AER than by GHG during the 1955–1984 period, when the strongest global AER increase. This stronger AER-induced AA is due to a greater sensitivity of Arctic sea ice, and associated changes in ocean-to-atmosphere heat exchange, to AER forcing. Our findings highlight the asymmetric Arctic climate response to GHG and AER forcings, and show that clean air policies which have reduced aerosol emissions may have exacerbated the Arctic warming over the past few decades. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email