Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Chemical composition, sources, and deposition fluxes of water-soluble inorganic ions obtained from precipitation chemistry measurements collected at an urban site in northwest China.

Precipitation samples were collected at an urban site in Xi'an, northwest China during March to November in 2009 and were then analyzed to determine the pH and concentrations of water-soluble inorganic ions (Na(+), NH(4)(+), K(+), Mg(2+), Ca(2+), SO(4)(2-), NO(3)(-), Cl(-), and F(-)) in precipitation. The pH of precipitation ranged from 4.1 to 7.6 for all of the samples with an annual volume-weighted mean of 6.4. While a large portion of the precipitation events were weakly acidic or alkaline, around 30% of the precipitation events in the autumn were strongly acidic. Precipitation events with air masses from the northeast and the southeast were weakly acidic while those with air masses from the northwest and the southwest were alkaline. SO(4)(2-), Ca(2+), NH(4)(+), and NO(3)(-) were dominant ions in the precipitation, accounting for 37%, 25%, 18%, and 9%, respectively, of the total analyzed ions. Ca(2+) and NH(4)(+) were found to be the major neutralizers of precipitation acidity; however, the contribution of Mg(2+), although much lower than those of Ca(2+) and NH(4)(+), was important, in many cases, in changing the precipitation from weakly acidic to weakly alkaline. Enrichment factor analysis confirmed that SO(4)(2-) and NO(3)(-) were produced from anthropogenic sources, Ca(2+), K(+), and 80% Mg(2+) were from crustal sources, and Na(+), Cl(-), and ∼20% of Mg(2+) were from marine sources. The annual wet depositions were estimated to be 3.5 t km(-2) per year for sulfur; 2.3 t km(-2) per year for nitrogen, of which 0.8 t km(-2) per year was oxidized nitrogen and 1.5 t km(-2) per year was reduced nitrogen; and 3.0 t km(-2) per year for Ca(2+).

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app