Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractLocalisation and seasonal positions of wireworms in soils    Next AbstractActivation of defence pathways in Scots pine bark after feeding by pine weevil (Hylobius abietis) »

J Environ Monit


Title:Direct measurements of urban OH reactivity during Nashville SOS in summer 1999
Author(s):Kovacs TA; Brune WH; Harder H; Martinez M; Simpas JB; Frost GJ; Williams E; Jobson T; Stroud C; Young V; Fried A; Wert B;
Address:"Department of Meteorology, The Pennsylvania State University, University Park, PA, USA"
Journal Title:J Environ Monit
Year:2003
Volume:5
Issue:1
Page Number:68 - 74
DOI: 10.1039/b204339d
ISSN/ISBN:1464-0325 (Print) 1464-0325 (Linking)
Abstract:"Emissions of volatile chemicals control the hydroxyl radical (OH), the atmosphere's main cleansing agent, and thus the production of secondary pollutants. Accounting for all of these chemicals can be difficult, especially in environments with mixed urban and forest emissions. The first direct measurements of the atmospheric OH reactivity, the inverse of the OH lifetime, were made as part of the Southern Oxidant Study (SOS) at Cornelia Fort Airpark in Nashville, TN in summer 1999. Measured OH reactivity was typically 11 s(-1). Measured OH reactivity was 1.4 times larger than OH reactivity calculated from the sum of the products of measured chemical concentrations and their OH reaction rate coefficients. This difference is statistically significant at the 1sigma uncertainty level of both the measurements and the calculations but not the 2sigma uncertainty level. Measured OH reactivity was 1.3 times larger than the OH reactivity from a model that uses measured ambient concentrations of volatile organic compounds (VOCs), NO, NO2, SO2, and CO. However, it was within approximately 10% of the OH reactivity from a model that includes hydrocarbon measurements made in a Nashville tunnel and scaled to the ambient CO at Cornelia Fort Airpark. These comparisons indicate that 30% of the OH reactivity in Nashville may come from short-lived highly reactive VOCs that are not usually measured in field intensive studies or by US EPA's Photochemical Assessment Monitoring Stations"
Keywords:Air Pollutants/*analysis Cities Environmental Monitoring Hydroxyl Radical/*analysis/*chemistry Organic Chemicals Oxidants/*analysis/*chemistry Seasons Tennessee Trees Volatilization;
Notes:"MedlineKovacs, T A Brune, W H Harder, H Martinez, M Simpas, J B Frost, G J Williams, E Jobson, T Stroud, C Young, V Fried, A Wert, B eng Research Support, U.S. Gov't, Non-P.H.S. England 2003/03/07 J Environ Monit. 2003 Feb; 5(1):68-74. doi: 10.1039/b204339d"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 05-11-2024