Identification

Title

Multi-scale modeling study of the source contributions to near-surface ozone and sulfur oxides levels over California during the ARCTAS-CARB period

Abstract

Chronic high surface ozone (Oâ‚ƒ) levels and the increasing sulfur oxides (SOx = SOâ‚‚+SOâ‚„) ambient concentrations over South Coast (SC) and other areas of California (CA) are affected by both local emissions and long-range transport. In this paper, multi-scale tracer, full-chemistry and adjoint simulations using the STEM atmospheric chemistry model are conducted to assess the contribution of local emission sourcesto SC Oâ‚ƒ and to evaluate the impacts of transported sulfur and local emissions on the SC sulfur budgetduring the ARCTAS-CARB experiment period in 2008. Sensitivity simulations quantify contributions of biogenic and fire emissions to SC O3 levels. California biogenic and fire emissions contribute 3â€“4 ppb to near-surface Oâ‚ƒ over SC, with larger contributions to other regions in CA. During a long-range transport event from Asia starting from 22 June, high SOx levels (up to âˆ¼0.7 ppb of SOâ‚‚ and âˆ¼1.3 ppb of SOâ‚„) is observed above âˆ¼6 km, but they did not affect CA surface air quality. The elevated SOx observed at 1-4 km is estimated to enhance surface SOx over SC by âˆ¼0.25 ppb (upper limit) on âˆ¼24 June. The near-surface SOx levels over SC during the flight week are attributed mostly to local emissions. Two anthropogenic SOx emission inventories (EIs) from the California Air Resources Board (CARB) and the US Environmental Protection Agency (EPA) are compared and applied in 60 km and 12 km chemical transport simulations, and the results are compared withobservations. The CARB EI shows improvements over the National Emission Inventory (NEI) by EPA, but generally underestimates surface SC SOx by about a factor of two. Adjoint sensitivity analysis indicated that SOâ‚‚ levels at 00:00 UTC (17:00 local time) at six SC surface sites were influenced by previous day maritime emissions over the ocean, the terrestrial emissions over nearby urban areas, and by transported SOâ‚‚ from the north through both terrestrial and maritime areas. Overall maritime emissions contribute 10-70% of SOâ‚‚ and 20-60% fine SOSOâ‚„ on-shore and over the most terrestrial areas, with contributions decreasing with in-land distance from the coast. Maritime emissions also modify the photochemical environment, shifting Oâ‚ƒ production over coastal SC to more VOC-limited conditions. These suggest an important role for shipping emission controls in reducing fine particle and Oâ‚ƒ concentrations in SC.

Resource type

document

Resource locator

Unique resource identifier

code

https://n2t.org/ark:/85065/d73f4qz9

codeSpace

Dataset language

eng

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code identifying the spatial reference system

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Topic category

geoscientificInformation

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keyword value

Text

originating controlled vocabulary

title

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reference date

date type

publication

effective date

2016-01-01T00:00:00Z

Geographic location

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East bounding longitude

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South bounding latitude

Temporal reference

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Dataset reference date

date type

publication

effective date

2011-04-04T00:00:00Z

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Conformity

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Use constraints

Limitations on public access

None

Responsible organisations

Responsible party

contact position

OpenSky Support

organisation name

UCAR/NCAR - Library

full postal address

PO Box 3000

Boulder

80307-3000

email address

opensky@ucar.edu

web address

http://opensky.ucar.edu/

name: homepage

responsible party role

pointOfContact

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