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Titel |
Impacts of transported background pollutants on summertime western US air quality: model evaluation, sensitivity analysis and data assimilation |
VerfasserIn |
M. Huang, G. R. Carmichael, T. Chai, R. B. Pierce, S. J. Oltmans, D. A. Jaffe, K. W. Bowman, A. Kaduwela, C. Cai, S. N. Spak, A. J. Weinheimer, L. G. Huey, G. S. Diskin |
Medientyp |
Artikel
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Sprache |
Englisch
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ISSN |
1680-7316
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Digitales Dokument |
URL |
Erschienen |
In: Atmospheric Chemistry and Physics ; 13, no. 1 ; Nr. 13, no. 1 (2013-01-14), S.359-391 |
Datensatznummer |
250017555
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Publikation (Nr.) |
copernicus.org/acp-13-359-2013.pdf |
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Zusammenfassung |
The impacts of transported background (TBG) pollutants on western US ozone
(O3) distributions in summer 2008 are studied using the multi-scale
Sulfur Transport and dEposition Modeling system. Forward sensitivity
simulations show that TBG contributes ~30–35 ppb to the surface
Monthly mean Daily maximum 8-h Average O3 (MDA8) over Pacific Southwest
(US Environmental Protection Agency (EPA) Region 9, including California,
Nevada and Arizona) and Pacific Northwest (EPA Region 10, including
Washington, Oregon and Idaho), and ~10–17 ppm-h to the secondary
standard metric "W126 monthly index" over EPA Region 9 and
~3–4 ppm-h over Region 10. The strongest TBG impacts on W126 occur
over the grass/shrub-covered regions. Among TBG pollutants, O3 is the
major contributor to surface O3, while peroxyacetyl nitrate is the most
important O3 precursor species. W126 shows larger responses than MDA8 to
perturbations in TBG and stronger non-linearity to the magnitude of
perturbations. The TBG impacts on both metrics overall negatively correlate
to model vertical resolution and positively correlate to the horizontal
resolution.
The mechanisms that determine TBG contributions and their variation are
analyzed using trajectories and the receptor-based adjoint sensitivity
analysis, which demonstrate the connection between the surface O3 and
O3 aloft (at ~1–4 km) 1–2 days earlier. The probabilities of
airmasses originating from Mt. Bachelor (2.7 km) and 2.5 km above Trinidad
Head (THD) entraining into the boundary layer reach daily maxima of 66%
and 34% at ~03:00 p.m. Pacific Daylight Time (PDT), respectively,
and stay above 50% during 09:00 a.m.–04:00 p.m. PDT for those
originating 1.5 km above California's South Coast.
Assimilation of the surface in-situ measurements significantly reduced the
errors in the modeled surface O3 during a long-range transport episode
by ~5 ppb on average (up to ~17 ppb) and increased the estimated
TBG contributions by ~3 ppb. Available O3 vertical profiles from
Tropospheric Emission Spectrometer (TES), Ozone Monitoring Instrument (OMI)
and THD sonde identified this transport event, but assimilation of these
observations in this case did not efficiently improve the O3
distributions except near the sampling locations, due to their limited
spatiotemporal resolution and/or possible uncertainties. |
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