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.


  • NSF Public Access
  • Search Results
  • The Role of Midlatitude Cyclones in the Emission, Transport, Production, and Removal of Aerosols in the Northern Hemisphere
Title: The Role of Midlatitude Cyclones in the Emission, Transport, Production, and Removal of Aerosols in the Northern Hemisphere
Abstract We examine the distribution of aerosol optical depth (AOD) across 27,707 northern hemisphere (NH) midlatitude cyclones for 2005–2018 using retrievals from the Moderate Resolution Spectroradiometer (MODIS) sensor on the Aqua satellite. Cyclone‐centered composites show AOD enhancements of 20%–45% relative to background conditions in the warm conveyor belt (WCB) airstream. Fine mode AOD accounts for 68% of this enhancement annually. Relative to background conditions, coarse mode AOD is enhanced by more than a factor of two near the center of the composite cyclone, co‐located with high surface wind speeds. Within the WCB, MODIS AOD maximizes in spring, with a secondary maximum in summer. Cyclone‐centered composites of AOD from the Modern Era Retrospective analysis for Research and Applications, version 2 Global Modeling Initiative (M2GMI) simulation reproduce the magnitude and seasonality of the MODIS AOD composites and enhancements. M2GMI simulations show that the AOD enhancement in the WCB is dominated by sulfate (37%) and organic aerosol (25%), with dust and sea salt each accounting for 15%. MODIS and M2GMI AOD are 60% larger in North Pacific WCBs compared to North Atlantic WCBs and show a strong relationship with anthropogenic pollution. We infer that NH midlatitude cyclones account for 355 Tg yr−1of sea salt aerosol emissions annually, or 60% of the 30–80°N total. We find that deposition within WCBs is responsible for up to 35% of the total aerosol deposition over the NH ocean basins. Furthermore, the cloudy environment of WCBs leads to efficient secondary sulfate production.  more » « less
Award ID(s):
1901786
PAR ID:
10408172
Author(s) / Creator(s):
 ;  ;  
Publisher / Repository:
DOI PREFIX: 10.1029
Date Published:
Journal Name:
Journal of Geophysical Research: Atmospheres
Volume:
128
Issue:
6
ISSN:
2169-897X
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; ; ; ; ; ; ; ; et al (, Nature Geoscience)
    Abstract The Arctic warms nearly four times faster than the global average, and aerosols play an increasingly important role in Arctic climate change. In the Arctic, sea salt is a major aerosol component in terms of mass concentration during winter and spring. However, the mechanisms of sea salt aerosol production remain unclear. Sea salt aerosols are typically thought to be relatively large in size but low in number concentration, implying that their influence on cloud condensation nuclei population and cloud properties is generally minor. Here we present observational evidence of abundant sea salt aerosol production from blowing snow in the central Arctic. Blowing snow was observed more than 20% of the time from November to April. The sublimation of blowing snow generates high concentrations of fine-mode sea salt aerosol (diameter below 300 nm), enhancing cloud condensation nuclei concentrations up to tenfold above background levels. Using a global chemical transport model, we estimate that from November to April north of 70° N, sea salt aerosol produced from blowing snow accounts for about 27.6% of the total particle number, and the sea salt aerosol increases the longwave emissivity of clouds, leading to a calculated surface warming of +2.30 W m−2under cloudy sky conditions. 
    more » « less
  2. ; ; ; ; ; ; ; ; ; ; et al (, Proceedings of the National Academy of Sciences)
    Anthropogenic ammonia (NH3) emissions have significantly increased in recent decades due to enhanced agricultural activities, contributing to global air pollution. While the effects of NH3on surface air quality are well documented, its influence on particle dynamics in the upper troposphere-lower stratosphere (UTLS) and related aerosol impacts remain unquantified. NH3reaches the UTLS through convective transport and can enhance new particle formation (NPF). This modeling study evaluates the global impact of anthropogenic NH3on UTLS particle formation and quantifies its effects on aerosol loading and cloud condensation nuclei (CCN) abundance. We use the EMAC Earth system model, incorporating multicomponent NPF parameterizations from the CERN CLOUD experiment. Our simulations reveal that convective transport increases NH3-driven NPF in the UTLS by one to three orders of magnitude compared to a baseline scenario without anthropogenic NH3, causing a doubling of aerosol numbers over high-emission regions. These aerosol changes induce a 2.5-fold increase in upper tropospheric CCN concentrations. Anthropogenic NH3emissions increase the relative contribution of water-soluble inorganic ions to the UTLS aerosol optical depth (AOD) by 20% and increase total column AOD by up to 80%. In simulations without anthropogenic NH3, UTLS aerosol composition is dominated by sulfate and organic species, with a marked reduction in ammonium nitrate and aerosol water content. This results in a decline of aerosol mass concentration by up to 50%. These findings underscore the profound global influence of anthropogenic NH3emissions on UTLS particle formation, AOD, and CCN production, with important implications for cloud formation and climate. 
    more » « less
  3. ; ; ; (, Geophysical Research Letters)
    Abstract Inorganic salts present in the atmosphere may affect the composition and abundance of secondary organic aerosol. Here, we quantify the effects of salt identity, salt concentration (ionic strength), and solution pH on the partitioning of ambient water‐soluble organic gases (WSOCg) at a site in the eastern United States. The experimental pH (pH = 1–6) and ionic strengths (10−3–101 mol kg−1) span a wide range of conditions found in atmospheric particles, clouds, and fog droplets. Chloride salts (NaCl, NH4Cl, and KCl) exhibit a strong salting‐out effect at all ionic strengths >0.005 mol kg−1and pH = 1.8–6. In contrast, sulfate salts (Na2SO4, (NH4)2SO4, and K2SO4) induce both salting‐in and salting‐out behaviors, depending on ionic strength and pH. These results suggest that monovalent cations have minimal effect, while ionic strength, pH, and anion identity exert strong effects on the partitioning of ambient organic gases in the atmosphere. 
    more » « less
  4. ; ; ; ; ; ; ; ; ; ; et al (, Geophysical Research Letters)
    Abstract Aqueous‐phase uptake and processing of water‐soluble organic compounds can promote secondary organic aerosol (SOA) production. We evaluated the contributions of aqueous‐phase chemistry to summertime urban SOA at two sites in New York City. The relative role of aqueous‐phase processing varied with chemical and environmental conditions, with evident daytime SOA enhancements (e.g., >1 μg/m3) during periods with relative humidities (RH) exceeding 65% and often higher temperatures. Oxygenated organic aerosol (OOA) production was also sensitive to secondary inorganic aerosols, in part through their influence on aerosol liquid water. On average, high‐RH periods exhibited a 69% increase in less‐oxidized OOA production in Queens, NY. These enhancements coincided with southerly backward trajectories and greater inorganic aerosol concentrations, yet showed substantial intra‐city variability between Queens and Manhattan. The observed aqueous‐phase SOA production, even with historically low sulfate and nitrate aerosol loadings, highlights both opportunities and challenges for continued reductions in summertime PM2.5in urban communities. 
    more » « less
  5. ; ; ; ; ; ; ; ; ; ; et al (, Atmospheric Chemistry and Physics)
    Abstract. The climatic and health effects of aerosols are strongly dependent on the intra-annual variations in their loading and properties. While the seasonal variations of regional aerosol optical depth (AOD) have been extensively studied, understanding the temporal variations in aerosol vertical distribution and particle types is also important for an accurate estimate of aerosol climatic effects. In this paper, we combine the observations from four satellite-borne sensors and several ground-based networks to investigate the seasonal variations of aerosol column loading, vertical distribution, and particle types over three populous regions: the Eastern United States (EUS), Western Europe (WEU), and Eastern and Central China (ECC). In all three regions, column AOD, as well as AOD at heights above 800m, peaks in summer/spring, probably due to accelerated formation of secondary aerosols and hygroscopic growth. In contrast, AOD below 800m peaks in winter over WEU and ECC regions because more aerosols are confined to lower heights due to the weaker vertical mixing. In the EUS region, AOD below 800m shows two maximums, one in summer and the other in winter. The temporal trends in low-level AOD are consistent with those in surface fine particle (PM2.5) concentrations. AOD due to fine particles ( < 0.7µm diameter) is much larger in spring/summer than in winter over all three regions. However, the coarse mode AOD ( > 1.4µm diameter), generally shows small variability, except that a peak occurs in spring in the ECC region due to the prevalence of airborne dust during this season. When aerosols are classified according to sources, the dominant type is associated with anthropogenic air pollution, which has a similar seasonal pattern as total AOD. Dust and sea-spray aerosols in the WEU region peak in summer and winter, respectively, but do not show an obvious seasonal pattern in the EUS region. Smoke aerosols, as well as absorbing aerosols, present an obvious unimodal distribution with a maximum occurring in summer over the EUS and WEU regions, whereas they follow a bimodal distribution with peaks in August and March (due to crop residue burning) over the ECC region. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email