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Isoprene plays a critical role in air quality and climate. Photosynthesis (gross primary productivity, GPP) and formaldehyde (HCHO) are both related to isoprene emission at large spatiotemporal scales, but neither is a perfect proxy. Here we apply multiple satellite products and site-level measurements to examine the impact of water deficit on the three interlinked variables at the Missouri Ozarks site during a 20-day mild dryness stress in summer 2011 and a 3-month severe drought in summer 2012. Isoprene emission shows opposite responses to the short- and long-term droughts, while GPP was substantially reduced in both cases. In 2012, both remote-sensedmore » solar-induced fluorescence (SIF) and satellite HCHO column qualitatively capture reductions in flux-derived GPP and isoprene emission, respectively, on weekly to monthly time scales, but with muted responses. For instance, as flux-derived GPP approaches zero in late summer 2012, SIF drops by 29–33% (July) and 19–27% (August) relative to year 2011. A possible explanation is that electron transport and photosystem activity are maintained to a certain extent under the drought stress. Similarly, flux tower isoprene emissions in July 2012 are 54% lower than July 2011, while the relative reductions in July for 3 independent satellite-derived HCHO data products are 27%, 12% and 6%, respectively. Finally, we attribute the muted HCHO response to a photochemical feedback whereby reduced isoprene emission increases the oxidation capacity available to generate HCHO from other volatile organic compound sources. Satellite SIF offers a potential alternative indirect method to monitor isoprene variability at large spatiotemporal scales from space, although further research is needed under different environmental conditions and regions. Our analysis indicates that fairly moderate reductions in satellite SIF and HCHO column may imply severe drought conditions at the surface.« less

Globally, secondary organic aerosol (SOA) is mostly formed from emissions of biogenic volatile organic compounds (VOCs) by vegetation, but it can be modified by human activities as demonstrated in recent research. Specifically, nitrogen oxides (NO_x = NO + NO₂) have been shown to play a critical role in the chemical formation of low volatility compounds. We have updated the SOA scheme in the global NCAR (National Center for Atmospheric Research) Community Atmospheric Model version 4 with chemistry (CAM4-chem) by implementing a 4-product volatility basis set (VBS) scheme, including NO_x-dependent SOA yields and aging parameterizations. Small differences are found for themore » no-aging VBS and 2-product schemes; large increases in SOA production and the SOA-to-OA ratio are found for the aging scheme. The predicted organic aerosol amounts capture both the magnitude and distribution of US surface annual mean measurements from the Interagency Monitoring of Protected Visual Environments (IMPROVE) network by 50 %, and the simulated vertical profiles are within a factor of 2 compared to aerosol mass spectrometer (AMS) measurements from 13 aircraft-based field campaigns across different regions and seasons. We then perform sensitivity experiments to examine how the SOA loading responds to a 50 % reduction in anthropogenic nitric oxide (NO) emissions in different regions. We find limited SOA reductions of 0.9–5.6, 6.4–12.0 and 0.9–2.8 % for global, southeast US and Amazon NO_x perturbations, respectively. The fact that SOA formation is almost unaffected by changes in NO_x can be largely attributed to a limited shift in chemical regime, to buffering in chemical pathways (low- and high-NO_x pathways, O₃ versus NO₃-initiated oxidation) and to offsetting tendencies in the biogenic versus anthropogenic SOA responses.« less