Comprehensive characterization of atmospheric organic carbon at a forested site

总有机碳 气溶胶 环境科学 环境化学 波动性(金融) 大气化学 空气质量指数 化学 大气科学 臭氧 气象学 有机化学 地质学 金融经济学 物理 经济
作者
James F. Hunter,Douglas A. Day,Brett B. Palm,R. L. N. Yatavelli,Arthur W. H. Chan,L. Kaser,Luca Cappellin,Patrick L. Hayes,Eben S. Cross,A. J. Carrasquillo,Pedro Campuzano‐Jost,Harald Stark,Yunliang Zhao,Thorsten Hohaus,James N. Smith,Armin Hansel,Thomas Karl,Allen H. Goldstein,Alex Guenther,Douglas R. Worsnop
出处
期刊:Nature Geoscience [Nature Portfolio]
卷期号:10 (10): 748-753 被引量:109
标识
DOI:10.1038/ngeo3018
摘要

Atmospheric organic compounds are central to key chemical processes that influence air quality, ecological health, and climate. However, longstanding difficulties in predicting important quantities such as organic aerosol formation and oxidant lifetimes indicate that our understanding of atmospheric organic chemistry is fundamentally incomplete, probably due in part to the presence of organic species that are unmeasured using standard analytical techniques. Here we present measurements of a wide range of atmospheric organic compounds—including previously unmeasured species—taken concurrently at a single site (a ponderosa pine forest during summertime) by five state-of-the-art mass spectrometric instruments. The combined data set provides a comprehensive characterization of atmospheric organic carbon, covering a wide range in chemical properties (volatility, oxidation state, and molecular size), and exhibiting no obvious measurement gaps. This enables the first construction of a measurement-based local organic budget, highlighting the high emission, deposition, and oxidation fluxes in this environment. Moreover, previously unmeasured species, including semivolatile and intermediate-volatility organic species (S/IVOCs), account for one-third of the total organic carbon, and (within error) provide closure on both OH reactivity and potential secondary organic aerosol formation. Atmospheric organic compounds are central to key chemical processes that influence air quality. Concurrent measurements of a wide range of these compounds, including previously unmeasured ones, provide closure on OH reactivity.
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