Abstract

Abstract. The Biosphere Effects on AeRosols and Photochemistry EXperiment (BEARPEX) took place in Blodgett Forest, a Ponderosa pine forest in the Sierra Nevada of California, USA, during summer 2009. We deployed a proton transfer reaction–quadrupole mass spectrometer (PTR-QMS) to measure fluxes and concentrations of biogenic volatile organic compounds (BVOCs). Eighteen ion species, including the major BVOC expected at the site, were measured sequentially at 5 heights to observe their vertical gradient from the forest floor to above the canopy. Fluxes of the 3 dominant BVOCs methanol, 2-Methyl-3-butene-2-ol (MBO), and monoterpenes were measured above the canopy by the disjunct eddy covariance (EC) method. Canopy-scale fluxes were also determined by the flux–gradient similarity method (K-theory). A universal K (Kuniv) was determined as the mean of individual K's calculated from the measured fluxes divided by vertical gradients for methanol, MBO, and monoterpenes. This Kuniv was then multiplied by the gradients of each observed ion species to compute their fluxes. The flux–gradient similarity method showed very good agreement with the disjunct EC method. Fluxes are presented for all measured species and compared to historical measurements from the same site, and used to test emission algorithms used to model fluxes at the regional scale. MBO was the dominant emission observed, followed by methanol, monoterpenes, acetone, and acetaldehyde. The flux–gradient similarity method is shown to be tenable, and we recommend its use, especially in experimental conditions when fast measurement of BVOC species is not available.

Highlights

  • Defining source strengths of biogenic volatile organic compounds (BVOC; e.g., isoprene and monoterpenes) and understanding their role in ozone (O3) and secondary organic aerosol (SOA) formation are critical issues in atmospheric chemistry and climate science (Chameides et al, 1988; Andreae and Crutzen, 1997; Fuentes et al, 2000; Jang et al, 2002)

  • Substantial evidence has been presented for the emissions of highly reactive BVOCs from forest ecosystems that have yet to be adequately quantified and included in BVOC emission models (Kurpius and Goldstein, 2003; Di Carlo et al, 2004; Holzinger et al, 2005)

  • (e) photosynthetically active radiation (PAR), and eddy covariance (EC) fluxes of All these compounds appear dependant on temperature, as (f) methanol, (g) MBO + isoprene and (h) monoterpenes

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Summary

Introduction

Defining source strengths of biogenic volatile organic compounds (BVOC; e.g., isoprene and monoterpenes) and understanding their role in ozone (O3) and secondary organic aerosol (SOA) formation are critical issues in atmospheric chemistry and climate science (Chameides et al, 1988; Andreae and Crutzen, 1997; Fuentes et al, 2000; Jang et al, 2002). Additional unmeasured organics in the atmosphere are assumed to exist in both the gas and particle phases (Goldstein and Galbally, 2007). More comprehensive observations are needed to better constrain the full range of BVOC emissions from ecosystems and their importance for atmospheric chemistry

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