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  1. 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.

     
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    Free, publicly-accessible full text available September 22, 2024
  2. Free, publicly-accessible full text available August 1, 2024
  3. 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.

     
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  4. Abstract

    Separating the climate response to external forcing from internal climate variability is a key challenge. While most previous studies have focused on surface responses, here we examine zonal‐mean patterns of North Pacific subsurface temperature responses. In particular, the changes since 1950 driven by anthropogenic aerosol emissions are found by using a pattern recognition method. Based on the single‐forcing large‐ensemble simulations from two models, we show that aerosol forcing caused a nonmonotonic temporal response and a characteristic zonal‐mean pattern within North Pacific, which is distinct from the pattern associated with internal variability. The aerosol‐forced pattern with the nonmonotonic temporal feature shows a substantial temperature change in subpolar regions and a reversed change on the southern flank of the subtropical gyre. A similar characteristic pattern and nonmonotonic time evolution are extracted from the subsurface observations, which likely reflect the subsurface responses to the aerosol forcing, although differences exist with the simulated responses.

     
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  5. Anthropogenic surface warming dominates and drives a global acceleration of the upper ocean currents in a warmer climate. 
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  6. 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.

     
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