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  • 2015-2019  (3)
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  • 1
    Publication Date: 2019-07-25
    Description: In situ aerosol extinction and absorption spectra covering the 300-700 nm range at 1 nm spectral resolution were measured aboard the R/V Onnuri during the Korea U.S. Ocean Color (KORUS-OC) cruise around the Korean Peninsula from May 21 through June 3, 2016. Total absorption spectra were obtained from aerosols collected on glass fiber filters and subsequently placed in the center of an integrating sphere (Labsphere DRA-CA-30) attached to a dual beam spectrophotometer (Cary 100 Bio UV-Visible Spectrophotometer, 0.2 nm spectral resolution). Absorption spectra from methanol and deionized water extracts of aerosols collected on Teflon filters were measured in a liquid waveguide capillary cell (World Precision Instruments LWCC- 3100, ~0.4 nm spectral resolution). Extinction spectra were measured with a custom built instrument (SpEx, ~0.8 nm spectral resolution). The measurements were obtained at a height of ~10 m above the sea surface with an inlet that limited the measured aerosols to diameters 1.3 m. All four sets of spectra exhibit curvature in log-log space with 2nd order polynomials providing a better fit to the measured spectra than power law fits. The deionized water extracts were also analyzed with an ion chromatograph (Dionex ICS-3000 Ion Chromatography System) and with an aerosol mass spectrometer (Aerodyne Research, Inc. HR-ToF High Resolution Aerosol Mass Spectrometer) to examine chemical composition. These data indicate the optical spectra are sensitive to differing chemical properties of the measured ambient aerosols and suggest differing sources and/or atmospheric processes influence the observed optical signatures. The measured suite of spectra are combined to examine the spectral characteristics of single scattering albedo, as well as to examine the contribution of soluble absorbing chromophores to the total absorption spectra. Additional measurements made during the affiliated Korea U.S. - Air Quality (KORUS-AQ) campaign will be used to provide further insight on the observed spectral characteristics.
    Keywords: Environment Pollution
    Type: GSFC-E-DAA-TN70994 , American Geophysical Union Fall Meeting; Dec 10, 2018 - Dec 14, 2019; Washington,DC; United States
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  • 2
    Publication Date: 2019-07-26
    Description: At the interface between the land, oceans, and atmosphere, coastal regions are highly dynamic environments, characterized by strong variability in both water and air quality. Variability in atmospheric composition is associated with highly variable anthropogenic emissions, as well as complex meteorological processes that influence the circulation and accumulation of atmospheric pollutants at the land-ocean interface. Assessing the spatial and temporal dynamics of atmospheric pollutants, aerosols, and absorbing trace gases in coastal areas is critical for improving modeling of coastal tropospheric air quality, developing accurate satellite retrievals of coastal ocean color and biological processes, determining impacts of atmospheric pollution on human health, and assessing the ecological implications of atmospheric pollutant deposition for coastal terrestrial and aquatic ecosystems.Here, we present new measurements of atmospheric trace gas (NO2, and ozone) dynamics across a range of estuarine and coastal waters near urban regions. Measurements were conducted from research vessels using NASA's shipboard Pandora spectrometers, as part of recent multidisciplinary, multiplatform field campaigns, including the 2016 KORUS OC/AQ field campaign in the Yellow Sea and East Sea/Sea of Japan, the 2017/2018 OLWETS field campaign in the Chesapeake Bay estuary, and the 2018 LISTOS field campaign in the Long Island Sound. Shipboard measurements over these coastal waters were integrated with measurements from a ground-based Pandora network to examine differences in air quality over the land and over the ocean. Measurements were combined with air-parcel back-trajectory simulations to determine the origin of air masses over the coastal ocean. Comparisons with satellite retrievals of atmospheric composition reveal the benefits and limitations of polar-orbit satellite observations in capturing variability in atmospheric pollution gradients over land-water boundaries.
    Keywords: Earth Resources and Remote Sensing
    Type: GSFC-E-DAA-TN71005 , American Geospysical Union 2018; Dec 10, 2018 - Dec 14, 2018; Washington, DC; United States
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  • 3
    Publication Date: 2019-11-16
    Description: Coastal environments are highly dynamic, and are characterized by short-term, local-scale variability in atmospheric and oceanic processes. Yet, high-frequency measurements of atmospheric composition, and particularly nitrogen dioxide (NO2) and ozone (O3) dynamics, are scarce over the ocean, introducing uncertainties in satellite retrievals of coastal ocean biogeochemistry and ecology. Combining measurements from different platforms, the Korea-US Ocean Color and Air Quality field campaign provided a unique opportunity to capture, for the first time, the strong spatial dynamics and diurnal variability in total column (TC) NO2 and O3 over the coastal waters of South Korea. Measurements were conducted using a shipboard Pandora Spectrometer Instrument specifically designed to collect accurate, high-frequency observations from a research vessel, and were combined with ground-based observations at coastal land sites, synoptic satellite imagery, and air-mass trajectory simulations to assess source contributions to atmospheric pollution over the coastal ocean. TCO3 showed only small (〈20%) variability that was driven primarily by larger-scale meteorological processes captured successfully in the relatively coarse satellite imagery from Aura-OMI. In contrast, TCNO2 over the ocean varied by more than an order of magnitude (0.070.92 DU), mostly affected by urban emissions and highly dynamic air mass transport pathways. Diurnal patterns varied widely across the ocean domain, with TCNO2 in the coastal area of Geoje and offshore Seoul varying by more than 0.6 DU and 0.4 DU, respectively, over a period of less than 3 h. On a polar orbit, Aura-OMI is not capable of detecting these short-term changes in TCNO2. If unaccounted for in atmospheric correction retrievals of ocean color, the observed variability in TCNO2 would be misinterpreted as a change in ocean remote sensing reflectance, R(sub rs), by more than 80% and 40% at 412 and 443 nm, respectively, introducing a significant false variability in retrievals of coastal ocean ecological processes from space.
    Keywords: Earth Resources and Remote Sensing
    Type: GSFC-E-DAA-TN70935 , Remote Sensing (e-ISSN 2072-4292); 10; 10; 1587
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