edu.ucar.opensky::articles:12039 UCAR/NCAR - Library OpenSky Support PO Box 3000 Boulder CO 80307-3000 opensky@ucar.edu http://opensky.ucar.edu/ homepage pointOfContact 2025-12-26T04:07:07.952441 ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data ISO 19115-2:2009(E) https://n2t.org/ark:/85065/d7mg7q6k Budgets for nocturnal VOC oxidation by nitrate radicals aloft during the 2006 Texas Air Quality Study 2011-12-28T00:00:00Z publication https://n2t.org/ark:/85065/d7mg7q6k https://doi.org/10.1029/2011JD016544 Brown, S. author Dube, W. author Peischl, J. author Ryerson, T. author Atlas, E. author Warneke, C. author De Gouw, J. author Hekkert, S. author Brock, C. author Flocke, Frank M. author Trainer, M. author Parrish, D. author Feshenfeld, F. author Ravishankara, A. author UCAR/NCAR - Library publisher Industrial emissions in Houston, Texas, and along the U.S. Gulf Coast are a large source of highly reactive anthropogenic volatile organic compounds (VOCs), principally alkenes, that affect air quality in that region. Nighttime oxidation by either O₃ or NO₃ removes these VOCs. This paper presents a regional analysis of nighttime P-3 flights during the 2006 Texas Air Quality Study (TexAQS) to quantify the loss rates and budgets for both NO₃ and highly reactive VOC. Mixing ratios and production rates of NO₃ were large, up to 400 parts per trillion by volume (pptv) and 1-2 parts per billion by volume (ppbv) per hour, respectively. Budgets for NO₃ show that it was lost primarily to reaction with VOCs, with the sum of anthropogenic VOCs (30-54%) and isoprene (10-50%) being the largest contributors. Indirect loss of NO₃ to N₂O₅ hydrolysis was of lesser importance (14-28%) but was the least certain due to uncertainty in the aerosol uptake coefficient for N₂O₅. Reaction of NO₃ with peroxy radicals was a small but nonzero contribution to NO₃ loss but was also uncertain because there were no direct measurements of peroxy radicals. Net VOC oxidation rates were rapid (up to 2 ppbv VOC h⁻¹ in industrial plumes) and were dominated by NO₃, which was 3-5 times more important as an oxidant than O₃. Plumes of high NO₃ reactivity (i.e., short steady state lifetimes, on the order of 1 min) identified the presence of concentrated emissions of highly reactive VOCs from the Houston Ship Channel (HSC), which, depending on the particular VOC, may be efficiently oxidized during overnight transport. UCAR/NCAR - Library OpenSky Support PO Box 3000 Boulder CO 80307-3000 opensky@ucar.edu http://opensky.ucar.edu/ homepage pointOfContact PDF Text theme Resource Type 2016-01-01T00:00:00Z publication Copyright 2011 American Geophysical Union. None eng geoscientificInformation