JEQ Journal of Natural Resources and Life Sciences Education
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text Free
Right arrow Full Text (PDF) Free
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Web of Science (4)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schade, G. W.
Right arrow Articles by Goldstein, A. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schade, G. W.
Right arrow Articles by Goldstein, A. H.
GeoRef
Right arrow GeoRef Citation
Agricola
Right arrow Articles by Schade, G. W.
Right arrow Articles by Goldstein, A. H.
Related Collections
Right arrow Organic Compounds
Right arrow Air Pollution
Journal of Environmental Quality 31:1088-1094 (2002)
© 2002 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America

TECHNICAL REPORTS
Atmospheric Pollutants and Trace Gases

Atmospheric Methyl Tertiary Butyl Ether (MTBE) at a Rural Mountain Site in California

Gunnar W. Schade*, Gabrielle B. Dreyfus and Allen H. Goldstein

University of California at Berkeley, Dep. of Environmental Science, Policy, and Management (ESPM), Ecosystem Science Division, 151 Hilgard Hall, Berkeley, CA 94720-3110

* Corresponding author (gws{at}nature.Berkeley.edu)

Received for publication August 15, 2001. Methyl tertiary butyl ether (MTBE) was measured in air samples collected at hourly intervals near Blodgett Forest Research Station on the western slope of the Sierra Nevada, California, in July 1997, October 1998, and June through September 1999. Mixing ratios ranged from below the detection limit (< approximately 0.01 ppbv) to 0.5 ppbv, but were generally less than 0.3 ppbv. At these mixing ratios partitioning of MTBE into surface waters would lead to MTBE concentrations of less than 0.2 µg L-1. As expected, MTBE mixing ratios were highly correlated with other anthropogenically emitted hydrocarbons. Based on the observed diurnal cycle of MTBE and its ratio to 2-methyl-butane (isopentane), we estimated the average regional daytime oxidant concentration to be (9 to 13) x 106 OH radicals per cubic centimeter, consistent with our earlier estimates for this region. Furthermore, MTBE ratios to toluene, another ubiquitous anthropogenic hydrocarbon, were generally consistent with regional transport and dilution, as well as atmospheric oxidation. Exceptions, pertaining to MTBE mixing ratios below or close to the detection limit, were associated with the influence of marine air masses that did not experience anthropogenic hydrocarbon input from California. With all these constraints in place, evidence for an additional atmospheric loss process, such as nonreversible deposition of MTBE, could not be established, and we conclude that any deposition is slow compared with removal from the atmosphere by the OH radical.

Abbreviations: MTBE, methyl tertiary butyl ether • ppbv, parts per billion by volume (1 ppbv MTBE = 3.61 µg m-3)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
The SCI Journals Agronomy Journal Crop Science
Journal of Natural Resources
and Life Sciences Education
Vadose Zone Journal
Soil Science Society of America Journal Journal of Plant Registrations The Plant Genome
Copyright © 2002 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America.