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AGU: Journal of Geophysical Research, Atmospheres

 

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  • Atmospheric Composition and Structure: Aerosols and particles
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Abstract
Cited By (16)
 

Abstract

Marine biogenic and anthropogenic contributions to non-sea-salt sulfate in the marine boundary layer over the North Atlantic Ocean

Dennis L. Savoie

Division of Marine and Atmospheric Chemistry, University of Miami, Miami, Florida, USA

Richard Arimoto

CEMRC, New Mexico State University, Carlsbad, New Mexico, USA

William C. Keene

Department of Environmental Sciences, University of Virginia, Charlottesville, Virginia, USA

Joseph M. Prospero

Division of Marine and Atmospheric Chemistry, University of Miami, Miami, Florida, USA

Robert A. Duce

College of Geosciences and Maritime Studies, Texas A&M University, College Station, Texas, USA

James N. Galloway

Department of Environmental Sciences, University of Virginia, Charlottesville, Virginia, USA

As a part of the Atmosphere/Ocean Chemistry Experiment (AEROCE), daily aerosol samples were collected in the marine boundary layer at Barbados, West Indies (13.17°N, 59.43°W), Bermuda (32.27°N, 64.87°W), and Mace Head, Ireland (53.32°N, 9.85°W), and in the free troposphere at Izaña, Tenerife, Canary Islands (28.30°N, 16.48°W; 2360 m asl). In this report, we use multiple variable regression analyses with methanesulfonate (MSA) and Sb and/or NO3 as the independent variables to assess the relative contributions of the marine biogenic and anthropogenic sources to the total non-sea-salt (nss) SO42− concentrations at the AEROCE sites. On the basis of 2 years of data at Bermuda and Barbados, the marine nss SO42−/MSA mass ratios (19.6 ± 2.1 and 18.8 ± 2.2) were consistent throughout the year and comparable to those at American Samoa in the tropical South Pacific (18.1 ± 0.9). At Mace Head (based on 1 year of data), this ratio was about 3.01 (±0.53). An analysis of the residuals and an assessment of the root mean square deviations indicate that the ratio at Mace Head can also be reasonably applied throughout the year. However, there is enough uncertainty during the winter that we cannot rule out a significant increase (to about 20) during periods with low concentrations of both MSA and NO3. The results from 4 years indicate that the marine contribution is too low to permit a reasonable assessment of the biogenic nss SO42−/MSA ratio at Izaña. The continental nss SO42−/Sb mass ratio varies significantly from one location to another. At Bermuda, where North American sources are expected to dominate, the ratio is about 29,000, about a factor of 2 higher than the average of 13,500 at Mace Head where European sources dominate. Intermediate values occurred at Barbados (18,000) and Izaña (24,000) where both European and North African sources are significant. Estimates based on these ratios indicate that, on an annual basis, the contributions from anthropogenic sources account for about 50% of the total nss SO42− in aerosols at Barbados, 70% at Bermuda, 85–90% at Mace Head, and about 90% at Izaña. If the same biogenic nss SO42−/MSA ratios are applicable to rainwater, then the relative contributions in precipitation at Barbados and Bermuda are comparable to those in aerosols.

Published 25 September 2002.

Citation: Savoie, D. L., R. Arimoto, W. C. Keene, J. M. Prospero, R. A. Duce, and J. N. Galloway (2002), Marine biogenic and anthropogenic contributions to non-sea-salt sulfate in the marine boundary layer over the North Atlantic Ocean, J. Geophys. Res., 107(D18), 4356, doi:10.1029/2001JD000970.

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