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000010530 084__ $$2WoS$$aMeteorology & Atmospheric Sciences
000010530 1001_ $$0P:(DE-HGF)0$$aDlugi, R.$$b0
000010530 245__ $$aTurbulent exchange and segregation of HOx radicals and volatile organic compounds above a deciduous forest
000010530 260__ $$aKatlenburg-Lindau$$bEGU$$c2010
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000010530 440_0 $$09601$$aAtmospheric Chemistry and Physics$$v10$$x1680-7316$$y13
000010530 500__ $$aThis research was financially supported by the German Atmospheric Research Program 2000, project ECHO under grant No. 07ATF47. In addition, three of us (Ralph Dlugi, Martina Berger, Michael Zelger) were supported by special funding of Forschungszentrum Julich, Germany.The very valuable and detailed comments from two well knowledgeable and informed reviewers were most helpful. We also greatly appreciate comments by F. Rohrer to different versions of the manuscript. We thank M. Schatzmann, B. Leitl and the staff of the Meteorological Institute, University of Hamburg, Germany and H. J. Kirtzel, METEK GmbH, Germany for their generous support to calibrate the sonic anemometers in the Environmental Wind Tunnel Laboratory, Hamburg.
000010530 520__ $$aThe eddy covariance method was applied for the first time to estimate fluxes of OH and HO2 together with fluxes of isoprene, the sum of methyl vinyl ketone (MVK) and methacrolein (MACR) and the sum of monoterpenes above a mixed deciduous forest. Highly sensitive measurements of OH and HO2 were performed by laser induced fluorescence (LIF), and biogenic volatile organic compounds (BVOCs) were measured by Proton-Transfer-Reaction Mass Spectrometry (PTR-MS) at a time resolution of 5 s, each. Wind speed was measured by a sonic anemometer at 10 Hz. The one-day feasibility study was conducted at a total height of 37 m, about 7 m above forest canopy, during the ECHO (Emission and CHemical transformation of biogenic volatile Organic compounds) intensive field study in July 2003. The daytime measurements yielded statistically significant OH fluxes directed downward into the direction of the canopy and HO2 fluxes mainly upward out of the canopy. This hints towards a significant local chemical sink of OH by reactions with BVOCs, other organic and inorganic compounds and conversion of OH to HO2 above the canopy. For OH the measured flux is locally balanced by chemical sources and sinks and direct transport of OH plays no important role for the local chemical OH budget at the measurement height, as expected from the short OH lifetime (<1 s). For HO2 the chemical lifetime (20 s) is in the range of the turbulent transport time for transfer between the top of the canopy and the measuring point. In this case, the radical balance is significantly influenced by both chemistry and transport processes. In addition, the highly time-resolved trace gas measurements were used to calculate the intensity of segregation of OH and BVOCs, demonstrating that the effective reaction rate of isoprene and OH was slowed down as much as 15% due to inhomogeneous mixing of the reactants. The paper describes the results, the applied methods and provides a detailed analysis of possible systematic errors of the covariance products.
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000010530 7001_ $$0P:(DE-HGF)0$$aBerger, M.$$b1
000010530 7001_ $$0P:(DE-HGF)0$$aZelger, M.$$b2
000010530 7001_ $$0P:(DE-Juel1)16326$$aHofzumahaus, A.$$b3$$uFZJ
000010530 7001_ $$0P:(DE-Juel1)VDB1526$$aSiese, M.$$b4$$uFZJ
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000010530 7001_ $$0P:(DE-HGF)0$$aWisthaler, A.$$b6
000010530 7001_ $$0P:(DE-HGF)0$$aGrabmer, W.$$b7
000010530 7001_ $$0P:(DE-HGF)0$$aHansel, A.$$b8
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000010530 773__ $$0PERI:(DE-600)2069847-1$$a10.5194/acp-10-6215-2010$$gVol. 10, p. 6215 - 6235$$p6215 - 6235$$q10<6215 - 6235$$tAtmospheric chemistry and physics$$v10$$x1680-7316$$y2010
000010530 8567_ $$uhttp://dx.doi.org/10.5194/acp-10-6215-2010
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