scholarly journals Boreal forest soil is a significant and diverse source of volatile organic compounds

2018 ◽  
Author(s):  
Mari Mäki ◽  
Hermanni Aaltonen ◽  
Jussi Heinonsalo ◽  
Heidi Hellén ◽  
Jukka Pumpanen ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Forest Soil ◽  
Organic Compounds ◽  
Coniferous Forest ◽  
Soil Surface ◽  
Surface Flux ◽  
Gas Diffusion ◽  
Oxidation Products ◽  
Volatile Organic ◽  
Flux Measurements

Abstract. Vegetation emissions of volatile organic compounds (VOCs) are intensively studied world-wide because oxidation products of VOCs contribute to atmospheric processes, but the quantities by which different species of VOCs are produced by soil, or how effectively belowground VOCs are released into the atmosphere from soil remains largely unknown. This is the first published study that measures belowground VOC concentrations at different depths in a podzol combined with simultaneous soil surface flux measurements in a boreal coniferous forest. More than 50 VOCs, dominated by monoterpenes and sesquiterpenes, were detected in the air space in the soil during the two measurement campaigns. Organic forest soil was a significant monoterpene source as it contained fresh isoprenoid-rich litter, and the concentrations of monoterpenes were comparable to the VOC concentrations in the air above the coniferous forest. Belowground monoterpene concentrations were largely decoupled from forest floor monoterpene fluxes; thus, it seems that production processes and storages of VOCs partly differ from those VOCs that are simultaneously emitted from the soil surface. Relatively high isoprenoid concentrations were measured under snow cover, which indicates that snow and ice cover hinders gas diffusion and causes belowground accumulation of VOCs when the activity of vegetation is very low.

scholarly journals Cryptogamic organisms are a substantial source and sink for volatile organic compounds in the Amazon region

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Achim Edtbauer ◽  
Eva Y. Pfannerstill ◽  
Ana Paula Pires Florentino ◽  
Cybelli G. G. Barbosa ◽  
Emilio Rodriguez-Caballero ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Atmospheric Chemistry ◽  
Forest Canopy ◽  
Oxidation Products ◽  
Atmospheric Oxidation ◽  
Tropical Rainforests ◽  
Volatile Organic ◽  
Flux Measurements ◽  
Made In

AbstractCryptogamic organisms such as bryophytes and lichens cover most surfaces within tropical forests, yet their impact on the emission of biogenic volatile organic compounds is unknown. These compounds can strongly influence atmospheric oxidant levels as well as secondary organic aerosol concentrations, and forest canopy leaves have been considered the dominant source of these emissions. Here we present cuvette flux measurements, made in the Amazon rainforest between 2016–2018, and show that common bryophytes emit large quantities of highly reactive sesquiterpenoids and that widespread lichens strongly uptake atmospheric oxidation products. A spatial upscaling approach revealed that cryptogamic organisms emit sesquiterpenoids in quantities comparable to current canopy attributed estimates, and take up atmospheric oxidation products at rates comparable to hydroxyl radical chemistry. We conclude that cryptogamic organisms play an important and hitherto overlooked role in atmospheric chemistry above and within tropical rainforests.

scholarly journals First eddy covariance flux measurements of semi-volatile organic compounds with the PTR3-TOF-MS

2021 ◽  
Vol 14 (12) ◽  
pp. 8019-8039
Author(s):  
Lukas Fischer ◽  
Martin Breitenlechner ◽  
Eva Canaval ◽  
Wiebke Scholz ◽  
Marcus Striednig ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Eddy Covariance ◽  
Organic Compounds ◽  
Oxidation Products ◽  
Concentration Data ◽  
Single Digit ◽  
Volatile Organic ◽  
Flux Measurements ◽  
Flight Reaction ◽  
Tof Ms

Abstract. We present first eddy covariance flux measurements with the PTR3-TOF-MS, a novel proton transfer time of flight reaction mass spectrometer. During 3 weeks in spring 2016, the instrument recorded 10 Hz data of biogenic volatile organic compounds above a boreal forest, on top of a measurement tower at the SMEAR (Station for Measuring Ecosystem –Atmosphere Relations) II station in Hyytiälä, Finland. Flux and concentration data of isoprene, monoterpenes, and sesquiterpenes were compared to the literature. Due to the improved instrument sensitivity and a customized wall-less inlet design, we could detect fluxes of semi-volatile and low-volatility organic compounds with less than single-digit picomol per square meter per second (pmolm-2s-1) values for the first time. These compounds include sesquiterpene oxidation products and diterpenes. Daytime diterpene fluxes were in the range of 0.05 to 0.15 pmolm-2s-1, which amounts to about 0.25 % to 0.5 % of the daytime sesquiterpene flux above canopy.

scholarly journals First Eddy Covariance Flux Measurements of Semi Volatile Organic Compounds with the PTR3-TOF-MS

2021 ◽  
Author(s):  
Lukas Fischer ◽  
Martin Breitenlechner ◽  
Eva Canaval ◽  
Wiebke Scholz ◽  
Marcus Striednig ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Eddy Covariance ◽  
Organic Compounds ◽  
Proton Transfer Reaction ◽  
Oxidation Products ◽  
Concentration Data ◽  
Single Digit ◽  
Volatile Organic ◽  
Flux Measurements ◽  
Tof Ms

Abstract. We present first eddy covariance flux measurements with the PTR3-TOF-MS, a novel proton-transfer-reaction mass-spectrometer (PTR-MS). During three weeks in spring 2016 the instrument recorded 10 Hz BVOC data on top of the SMEAR II tower in Hyytiälä, Finland. Flux and concentration data of isoprene, monoterpenes and sesquiterpenes were compared to the literature. Due to the improved instrument sensitivity and a customized “wall less” inlet design we could detect a number of fluxes of semi-volatile and low volatile organic compounds (SVOC and LVOC) with less than single digit picomol/m2/s values for the first time. These compounds include sesquiterpene oxidation products and diterpenes. Daytime diterpene fluxes were in the range of 0.05 to 0.15 picomol/m2/s, which amounts to about 0.25 % to 0.5 % of the daytime sesquiterpene flux above canopy.

scholarly journals Measurements of volatile organic compounds over West Africa

2010 ◽  
Vol 10 (2) ◽  
pp. 3861-3892 ◽  
Author(s):  
J. G. Murphy ◽  
D. E. Oram ◽  
C. E. Reeves
Keyword(s):  
Boundary Layer ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Marine Boundary Layer ◽  
Deep Convection ◽  
Proton Transfer Reaction ◽  
Oxidation Products ◽  
High Time Resolution ◽  
Airborne Measurements ◽  
Volatile Organic

Abstract. In this paper we describe measurements of volatile organic compounds (VOCs) made using a Proton Transfer Reaction Mass Spectrometer (PTR-MS) aboard the UK Facility for Atmospheric Airborne Measurements during the African Monsoon Multidisciplinary Analyses (AMMA) campaign. Observations were made during approximately 85 h of flying time between 17 July and 17 August 2006, above an area between 4° N and 18° N and 3° W and 4° E, encompassing ocean, mosaic forest, and the Sahel desert. High time resolution observations of counts at mass to charge (m/z) ratios of 42, 59, 69, 71, and 79 were used to calculate mixing ratios of acetonitrile, acetone, isoprene, the sum of methyl vinyl ketone and methacrolein, and benzene, respectively using laboratory-derived humidity-dependent calibration factors. Strong spatial associations between vegetation and isoprene and its oxidation products were observed in the boundary layer, consistent with biogenic emissions followed by rapid atmospheric oxidation. Acetonitrile, benzene, and acetone were all enhanced in airmasses which had been heavily influenced by biomass burning. Benzene and acetone were also elevated in airmasses with urban influence from cities such as Lagos, Cotonou, and Niamey. The observations provide evidence that both deep convection and mixing associated with fair-weather cumulus were responsible for vertical redistribution of VOCs emitted from the surface. Profiles over the ocean showed a depletion of acetone in the marine boundary layer, but no significant decrease for acetonitrile.

scholarly journals Boreal forest soil is a significant and diverse source of volatile organic compounds

2019 ◽  
Vol 441 (1-2) ◽  
pp. 89-110 ◽  
Author(s):  
Mari Mäki ◽  
Hermanni Aaltonen ◽  
Jussi Heinonsalo ◽  
Heidi Hellén ◽  
Jukka Pumpanen ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Boreal Forest ◽  
Forest Soil ◽  
Organic Compounds ◽  
Volatile Organic ◽  
Diverse Source

scholarly journals Contributions to OH reactivity from unexplored volatile organic compounds measured by PTR-ToF-MS – A case study in a suburban forest of the Seoul Metropolitan Area during KORUS-AQ 2016

2020 ◽  
Author(s):  
Dianne Sanchez ◽  
Roger Seco ◽  
Dasa Gu ◽  
Alex Guenther ◽  
John Mak ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Mass Spectrometer ◽  
Metropolitan Area ◽  
Forest Canopy ◽  
Oxidation Products ◽  
Ionization Mass ◽  
Seoul Metropolitan Area ◽  
Volatile Organic ◽  
Tof Ms

Abstract. We report OH reactivity observations by a chemical ionization mass spectrometer – comparative reactivity method (CIMS-CRM) instrument in a suburban forest of the Seoul Metropolitan Area (SMA) during Korea US Air Quality Study (KORUS-AQ 2016) from mid-May to mid-June of 2016. A comprehensive observational suite was deployed to quantify reactive trace gases inside of the forest canopy including a high-resolution proton transfer reaction time of flight mass spectrometer (PTR-ToF-MS). An average OH reactivity of 30.7 ± 5.1 s−1 was observed, while the OH reactivity calculated from CO, NO + NO2 (NOx), ozone (O3), sulfur dioxide (SO2), and 14 volatile organic compounds (VOCs) was 11.8 ± 1.0 s−1. An analysis of 346 peaks from the PTR-ToF-MS accounted for an additional 6.0 ± 2.2 s−1 of the total measured OH reactivity, leaving 42.0 % missing OH reactivity. The missing OH reactivity most likely comes from VOC oxidation products of both biogenic and anthropogenic origin.

scholarly journals Physicochemical uptake and release of volatile organic compounds by soil in coated-wall flow tube experiments with ambient air

2019 ◽  
Vol 19 (4) ◽  
pp. 2209-2232 ◽  
Author(s):  
Guo Li ◽  
Yafang Cheng ◽  
Uwe Kuhn ◽  
Rongjuan Xu ◽  
Yudong Yang ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Atmospheric Chemistry ◽  
Soil Surface ◽  
Ambient Air ◽  
Flow Tube ◽  
Heterogeneous Oxidation ◽  
Volatile Organic ◽  
Wall Flow

Abstract. Volatile organic compounds (VOCs) play a key role in atmospheric chemistry. Emission and deposition on soil have been suggested as important sources and sinks of atmospheric trace gases. The exchange characteristics and heterogeneous chemistry of VOCs on soil, however, are not well understood. We used a newly designed differential coated-wall flow tube system to investigate the long-term variability of bidirectional air–soil exchange of 13 VOCs under ambient air conditions of an urban background site in Beijing. Sterilized soil was investigated to address physicochemical processes and heterogeneous/multiphase reactions independently from biological activity. Most VOCs revealed net deposition with average uptake coefficients (γ) in the range of 10−7–10−6 (referring to the geometric soil surface area), corresponding to deposition velocities (Vd) of 0.0013–0.01 cm s−1 and soil surface resistances (Rc) of 98–745 s cm−1, respectively. Formic acid, however, was emitted at a long-term average rate of ∼6×10-3 nmol m−2 s−1, suggesting that it was formed and released upon heterogeneous oxidation of other VOCs. The soil–atmosphere exchange of one individual VOC species can be affected by both its surface degradation/depletion caused by surface reactions and by competitive uptake or heterogeneous formation/accommodation of other VOC species. Overall, the results show that physicochemical processing and heterogeneous oxidation on soil and soil-derived dust can act as a sink or as a source of atmospheric VOCs, depending on molecular properties and environmental conditions.

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

2018 ◽  
Author(s):  
Christian Nyrop Albers ◽  
Magnus Kramshøj ◽  
Riikka Rinnan
Keyword(s):  
Volatile Organic Compounds ◽  
Carbon Cycling ◽  
Organic Compounds ◽  
Soil Microbes ◽  
Coniferous Forest ◽  
Great Effort ◽  
Biogenic Volatile Organic Compounds ◽  
Arctic Soils ◽  
Beech Stand ◽  
Volatile Organic

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.

scholarly journals Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity

2008 ◽  
Vol 8 (4) ◽  
pp. 14273-14309 ◽  
Author(s):  
T. Karl ◽  
E. Apel ◽  
A. Hodzic ◽  
D. Riemer ◽  
D. Blake ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Eddy Covariance ◽  
Organic Compounds ◽  
Mexico City ◽  
Biomass Burning ◽  
Minor Role ◽  
Industrial Emissions ◽  
Tertiary Butyl ◽  
Volatile Organic ◽  
Flux Measurements

Abstract. Toluene and benzene are used for assessing the ability to measure disjunct eddy covariance (DEC) fluxes of Volatile Organic Compounds (VOC) using Proton Transfer Reaction Mass Spectrometry (PTR-MS) on aircraft. Statistically significant correlation between vertical wind speed and mixing ratios suggests that airborne VOC eddy covariance (EC) flux measurements using PTR-MS are feasible. City-average midday toluene and benzene fluxes are calculated to be on the order of 15.5±4.0 mg/m2/h and 4.7±2.3 mg/m2/h respectively. These values argue for an underestimation of toluene and benzene emissions in current inventories used for the Mexico City Metropolitan Area (MCMA). Wavelet analysis of instantaneous toluene and benzene measurements during city overpasses is tested as a tool to assess surface emission heterogeneity. High toluene to benzene flux ratios above an industrial district (e.g. 10–15) including the International airport (e.g. 3–5) and a mean flux (concentration) ratio of 3.2±0.5 (3.9±0.3) across Mexico City indicate that evaporative fuel and industrial emissions play an important role for the prevalence of aromatic compounds. Based on a tracer model, which was constrained by BTEX (Benzene/Toluene/Ethylbenzene/m,p,o-Xylenes) compound concentration ratios, the fuel marker methyl-tertiary-butyl-ether (MTBE) and the biomass burning marker acetonitrile (CH3CN), we show that a combination of industrial, evaporative fuel, and exhaust emissions account for >90% of all BTEX sources. Our observations suggest that biomass burning emissions play a minor role for the abundance of BTEX compounds (0–10%) in the MCMA.

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