Perchlorate in Wet Deposition Across North America

Authors

Srinath Rajagopalan, Texas Tech University
Todd A. Anderson, Texas Tech UniversityFollow
Stephen Cox, Texas Tech University
Greg Harvey, U.S. Air Force Air Force Material Command ASC/ENVR
Qiuqiong Cheng, University of Pittsburgh
W. Andrew Jackson, Texas Tech University

Date of this Version

2009

Comments

Published in ENVIRONMENTAL SCIENCE & TECHNOLOGY / VOL. 43, NO. 3, 2009.

Abstract

Natural perchlorate is believed to be of atmospheric origin, yet no systematic study has been conducted to evaluate perchlorate deposition rate and possible seasonal or spatial variations. This study evaluated perchlorate concentrations in weekly composite wet deposition samples acquired through the National Atmospheric DepositionProgramfrom 26 sites across the continental United States, Alaska, and Puerto Rico for a 1-3 year period. Perchlorate concentrations varied from /L to a high of 102 ng/L with a mean of 14.1±13.5 ng/L for the 1578 total samples. The annual perchlorate flux by site ranged from a low of 12.5 (TX) to 157 mg/ha-year (NE) and averaged 65 ± 30 mg/ha-year for all sites. Perchlorate concentrations and flux in wet deposition were generally highest in May-August declining to lows in December-February. Average annual perchlorate flux was correlated (r > 0.5; p < 0.001) with Ca²⁺, K⁺, NH₄⁺, NO₃^-, Cl^-, and SO₄ ^-2. Wet deposition rate of ClO₄^- in the conterminous United States (excluding Alaska, Hawaii, and Puerto Rico) while diffuse, represents a potential annual net mass flux of 51 000 kg, a value comparable to the estimated annual environmental releases from other known ClO₄ ^- sources.