scholarly journals Rapid mineralization of biogenic volatile organic compounds in temperate and Arctic soils

Author(s):  
Christian Nyrop Albers ◽  
Magnus Kramshøj ◽  
Riikka Rinnan

Abstract. Biogenic volatile organic compounds (BVOCs) are produced by all life forms. Their release into the atmosphere is important with regards to a number of physical and chemical processes and great effort has been put into determining sources and sinks of these compounds in recent years. Soil microbes as a possible sink for BVOCs in the atmosphere has been suggested, however, experimental evidence for this sink is scarce despite its potentially high importance to both carbon cycling and atmospheric concentrations of these gases. We therefore conducted a study with a number of commonly occurring BVOCs labelled with 14C and modified existing methods to study mineralization of these compounds to 14CO2 in four different top soils. Five of the six BVOCs were rapidly mineralized by microbes in all soils. However, great differences were observed with regards to speed of mineralization, extent of mineralization and variation between soil types. Methanol, benzaldehyde, acetophenone and the oxygenated monoterpene geraniol were mineralized within hours in all soils. The hydrocarbon monoterpene p-cymene was mineralized rapidly in soil from a coniferous forest but slower in soil from and adjacent beech stand while chloroform was mineralized slowly in all soils. From our study it is clear that soil microbes are able to degrade completely BVOCs released by aboveground vegetation as well as BVOCs released by soil microbes and plant roots. In addition to the possible atmospheric implications of this degradation the very fast mineralization rates are likely important in shaping the net BVOC emissions from soil and it is possible that BVOC formation and degradation may be an important but little recognized part of internal carbon cycling in soil.

2018 ◽  
Vol 15 (11) ◽  
pp. 3591-3601 ◽  
Author(s):  
Christian Nyrop Albers ◽  
Magnus Kramshøj ◽  
Riikka Rinnan

Abstract. Biogenic volatile organic compounds (BVOCs) are produced by all life forms. Their release into the atmosphere is important with regards to a number of climate-related physical and chemical processes and great effort has been put into determining sources and sinks of these compounds in recent years. Soil microbes have been suggested as a possible sink for BVOCs in the atmosphere; however, experimental evidence for this sink is scarce despite its potentially high importance to both carbon cycling and atmospheric concentrations of these gases. We therefore conducted a study with a number of commonly occurring BVOCs labelled with 14C and modified existing methods to study the mineralization of these compounds to 14CO2 in four different topsoils. Five of the six BVOCs were rapidly mineralized by microbes in all soils. However, great differences were observed with regards to the speed of mineralization, extent of mineralization and variation between soil types. Methanol, benzaldehyde, acetophenone and the oxygenated monoterpene geraniol were mineralized within hours in all soils. The hydrocarbon monoterpene p-cymene was mineralized rapidly in soil from a coniferous forest but was mineralized slower in soil from an adjacent beech stand, while chloroform was mineralized slowly in all soils. From our study it is clear that soil microbes are able to completely degrade BVOCs released by above-ground vegetation as well as BVOCs released by soil microbes and plant roots. In addition to the possible atmospheric implications of this degradation, the very fast mineralization rates are likely important in shaping the net BVOC emissions from soil and it is possible that BVOC formation and degradation may be important but little-recognized parts of internal carbon cycling in soil.


2011 ◽  
Vol 45 (34) ◽  
pp. 6191-6196 ◽  
Author(s):  
Yu Huang ◽  
Steven Sai Hang Ho ◽  
Kin Fai Ho ◽  
Shun Cheng Lee ◽  
Yuan Gao ◽  
...  

2016 ◽  
Vol 9 (5) ◽  
pp. 1959-1976 ◽  
Author(s):  
Chun Zhao ◽  
Maoyi Huang ◽  
Jerome D. Fast ◽  
Larry K. Berg ◽  
Yun Qian ◽  
...  

Abstract. Current climate models still have large uncertainties in estimating biogenic trace gases, which can significantly affect atmospheric chemistry and secondary aerosol formation that ultimately influences air quality and aerosol radiative forcing. These uncertainties result from many factors, including uncertainties in land surface processes and specification of vegetation types, both of which can affect the simulated near-surface fluxes of biogenic volatile organic compounds (BVOCs). In this study, the latest version of Model of Emissions of Gases and Aerosols from Nature (MEGAN v2.1) is coupled within the land surface scheme CLM4 (Community Land Model version 4.0) in the Weather Research and Forecasting model with chemistry (WRF-Chem). In this implementation, MEGAN v2.1 shares a consistent vegetation map with CLM4 for estimating BVOC emissions. This is unlike MEGAN v2.0 in the public version of WRF-Chem that uses a stand-alone vegetation map that differs from what is used by land surface schemes. This improved modeling framework is used to investigate the impact of two land surface schemes, CLM4 and Noah, on BVOCs and examine the sensitivity of BVOCs to vegetation distributions in California. The measurements collected during the Carbonaceous Aerosol and Radiative Effects Study (CARES) and the California Nexus of Air Quality and Climate Experiment (CalNex) conducted in June of 2010 provided an opportunity to evaluate the simulated BVOCs. Sensitivity experiments show that land surface schemes do influence the simulated BVOCs, but the impact is much smaller than that of vegetation distributions. This study indicates that more effort is needed to obtain the most appropriate and accurate land cover data sets for climate and air quality models in terms of simulating BVOCs, oxidant chemistry and, consequently, secondary organic aerosol formation.


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