Abundant Volatile Organic Compounds Research Articles

Volatile Organic Compounds (VOCs) from Wood and Wood-Based Panels: Methods for Evaluation, Potential Health Risks, and Mitigation.

Volatile organic compounds (VOCs) are contained in various construction materials and interior equipment. Their higher concentrations in the indoor air are associated with negative effects on human health and are disputed in terms of health risk, since people spend a considerable part of their lifetime indoors. Therefore, the presence of VOCs in indoor air is a case of concern regarding sick building syndrome (SBS). From a historical point of view, wood and wood-based panels represent a widely used material. Nevertheless, wood appears to be nowadays a product and a material of a sustainable future. Depending on wood extractives’ composition and an abundance of diverse wood species, different profiles of volatiles are emitted. In case of wood-based panels, the impact of adhesives and additives that are essentially applied aiming to adjust the panels’ properties is even enriching this cocktail of chemicals. This paper comprises the issue of VOCs emitted from wood and wood-based panels. The most abundant VOCs were summarized. The options of VOCs for analytical determination from these matrixes are described with their benefits and limitations.

An increasing role for solvent emissions and implications for future measurements of volatile organic compounds

Volatile organic compounds (VOCs) are a broad class of air pollutants which act as precursors to tropospheric ozone and secondary organic aerosols. Total UK emissions of anthropogenic VOCs peaked in 1990 at 2,840 kt yr−1 and then declined to approximately 810 kt yr−1 in 2017 with large reductions in road transport and fugitive fuel emissions. The atmospheric concentrations of many non-methane hydrocarbons (NMHC) in the UK have been observed to fall over this period in broadly similar proportions. The relative contribution to emissions from solvents and industrial processes is estimated to have increased from approximately 35% in 1990 to approximately 63% in 2017. In 1992, UK national monitoring quantified 19 of the 20 most abundant individual anthropogenic VOCs emitted (all were NMHCs), but by 2017 monitoring captured only 13 of the top 20 emitted VOCs. Ethanol is now estimated to be the most important VOC emitted by mass (in 2017 approx. 136 kt yr−1 and approx. 16.8% of total emissions) followed by n-butane (52.4 kt yr−1) and methanol (33.2 kt yr−1). Alcohols have grown in significance representing approximately 10% of emissions in 1990 rising to approximately 30% in 2017. The increased role of solvent emissions should now be reflected in European monitoring strategies to verify total VOC emission reduction obligations in the National Emissions Ceiling Directive. Adding ethanol, methanol, formaldehyde, acetone, 2-butanone and 2-propanol to the existing NMHC measurements would provide full coverage of the 20 most significant VOCs emitted on an annual mass basis.This article is part of a discussion meeting issue ‘Air quality, past present and future’.

Isoprene Reactivity on Water Surfaces from ab initio QM/MM Molecular Dynamics Simulations.

Isoprene is the most abundant volatile organic compound in the atmosphere after methane. While gas-phase processes have been widely studied, the chemistry of isoprene in aqueous environments is less well known. Nevertheless, some experiments have reported unexpected reactivity at the air-water interface. In this work, we have carried out combined quantum-classical molecular dynamics simulations of isoprene at the air-water interface, as well as ab initio and density functional theory calculations on isoprene-water complexes. We report the first calculation of the thermodynamics of adsorption of isoprene at the water surface, examine how hydration influences its electronic properties and reactivity indices, and estimate the OH-initiated oxidation rate. Our study indicates that isoprene interacts with the water surface mainly through H-π bonding. This primary interaction mode produces strong fluctuations of the π and π* bond stabilities, and therefore of isoprene's chemical potential, nucleophilicity and ionization potential, anticipating significant dynamical effects on its reactivity at the air-water interface. Using data from the literature and free energies reported in our work, we have estimated the rate of the OH-initiated oxidation process at the air-water interface (5.0×1012 molecule cm-3 s-1 ) to be about 7 orders of magnitude larger than the corresponding rate in the gas phase (8.2×105 molecule cm-3 s-1 ). Atmospheric implications of this result are discussed.

Fungal compound 1-octen-3-ol induces mitochondrial morphological alterations and respiration dysfunctions in Drosophila melanogaster

Fungal volatile organic compounds (VOCs) comprise a group of compounds commonly found in damp or water-damaged indoor places affecting air quality. Indoor fungal pollution is a severe threat to human health, contributing to the onset of allergic diseases. The compound 1-octen-3-ol, known as “mushroom alcohol”, is the most abundant VOC and confers the characteristic mold odor. Exposure to 1-octen-3-ol induces inflammatory markers and episodes of allergic rhinitis and conjunctivitis; however, the effects of this compound towards mitochondria are fairly known. The present study aimed to evaluate the effects of 1-octen-3-ol on inflammatory targets and on mitochondrial morphology and bioenergetic rate in D. melanogaster. Drosophilas were exposed by inhalation to 2.5 μL/L and 5 μL/L of 1-octen-3-ol for 24 h. Observation showed a decreasing in the survival and locomotor ability of flies. Superoxide dismutase (SOD) activity was induced whereas Catalase (CAT) activity was inhibited. Analysis of the mitochondria respiration, detected inhibition of complex I and II in the electron transport chain and a decreased bioenergetic rate. Electronic microscopy provided morphological insights of the mitochondrial status in which a disarrangement in mitochondrial cristae profile was observed. 1-Octen-3-ol induced increased activity of caspase 3/7 and ERK phosphorylation. The mRNA relative steady-state levels of p38MAPK and JNK were down-regulated, whereas NF-κB and p53 were up-regulated. In parallel, nitrite levels were induced in relation to the non-exposed group. These findings point to the mitochondria as a crucial target for the toxicity of 1-octen-3-ol in parallel with activation of pro-inflammatory factors and apoptotic signaling pathway cascade.

Respiratory CO2 Combined With a Blend of Volatiles Emitted by Endophytic Serendipita Strains Strongly Stimulate Growth of Arabidopsis Implicating Auxin and Cytokinin Signaling.

Rhizospheric microorganisms can alter plant physiology and morphology in many different ways including through the emission of volatile organic compounds (VOCs). Here we demonstrate that VOCs from beneficial root endophytic Serendipita spp. are able to improve the performance of in vitro grown Arabidopsis seedlings, with an up to 9.3-fold increase in plant biomass. Additional changes in VOC-exposed plants comprised petiole elongation, epidermal cell and leaf area expansion, extension of the lateral root system, enhanced maximum quantum efficiency of photosystem II (Fv/Fm), and accumulation of high levels of anthocyanin. Notwithstanding that the magnitude of the effects was highly dependent on the test system and cultivation medium, the volatile blends of each of the examined strains, including the references S. indica and S. williamsii, exhibited comparable plant growth-promoting activities. By combining different approaches, we provide strong evidence that not only fungal respiratory CO2 accumulating in the headspace, but also other volatile compounds contribute to the observed plant responses. Volatile profiling identified methyl benzoate as the most abundant fungal VOC, released especially by Serendipita cultures that elicit plant growth promotion. However, under our experimental conditions, application of methyl benzoate as a sole volatile did not affect plant performance, suggesting that other compounds are involved or that the mixture of VOCs, rather than single molecules, accounts for the strong plant responses. Using Arabidopsis mutant and reporter lines in some of the major plant hormone signal transduction pathways further revealed the involvement of auxin and cytokinin signaling in Serendipita VOC-induced plant growth modulation. Although we are still far from translating the current knowledge into the implementation of Serendipita VOCs as biofertilizers and phytostimulants, volatile production is a novel mechanism by which sebacinoid fungi can trigger and control biological processes in plants, which might offer opportunities to address agricultural and environmental problems in the future.

Exhaled breath compositions under varying respiratory rhythms reflects ventilatory variations: translating breathomics towards respiratory medicine

Control of breathing is automatic and its regulation is keen to autonomic functions. Therefore, involuntary and voluntary nervous regulation of breathing affects ventilatory variations, which has profound potential to address expanding challenges in contemporary pulmonology. Nonetheless, the fundamental attributes of the aforementioned phenomena are rarely understood and/or investigated. Implementation of unconventional approach like breathomics may leads to a better comprehension of those complexities in respiratory medicine. We applied breath-resolved spirometry and capnometry, non-invasive hemodynamic monitoring along with continuous trace analysis of exhaled VOCs (volatile organic compounds) by means of real-time mass-spectrometry in 25 young and healthy adult humans to investigate any possible mirroring of instant ventilatory variations by exhaled breath composition, under varying respiratory rhythms. Hemodynamics remained unaffected. Immediate changes in measured breath compositions and corresponding variations occurred when respiratory rhythms were switched between spontaneous (involuntary/unsynchronised) and/or paced (voluntary/synchronised) breathing. Such changes in most abundant, endogenous and bloodborne VOCs were closely related to the minute ventilation and end-tidal CO2 exhalation. Unprecedentedly, while preceded by a paced rhythm, spontaneous rhythms in both independent setups became reproducible with significantly (P-value ≤ 0.005) low intra- and inter-individual variation in measured parameters. We modelled breath-resolved ventilatory variations via alveolar isoprene exhalation, which were independently validated with unequivocal precision. Reproducibility i.e. attained via our method would be reliable for human breath sampling, concerning biomarker research. Thus, we may realize the actual metabolic and pathophysiological expressions beyond the everlasting in vivo physiological noise. Consequently, less pronounced changes are often misinterpreted as disease biomarker in cross-sectional studies. We have also provided novel information beyond conventional spirometry and capnometry. Upon clinical translations, our findings will have immense impact on pulmonology and breathomics as they have revealed a reproducible pattern of ventilatory variations and respiratory homeostasis in endogenous VOC exhalations.

Characteristics of VOCs generated during production and construction of an asphalt pavement

The Volatile Organic Compounds (VOCs) generated during asphalt pavement production and construction have negative impacts on both asphalt workers’ health and atmospheric ecosystem. The characteristics of asphalt VOCs have been partly investigated so far, thus hindering the proper accomplishment of mitigation strategies. To address this issue, this study conducted a comprehensive investigation on VOCs composition and concentration by means of Thermal Desorption-Gas Chromatography-Mass Spectrometry (TD-GC-MS). Air samples were collected during the production and the construction of an asphalt pavement located in Inner Mongolia, China, considering the four key locations for VOCs emissions: asphalt laboratory, mixing plant, asphalt storage tank and paving construction site. The analyses detected up to 135 different VOCs types. The asphalt storage tank was responsible for the most abundant VOCs emission, nearly 110 μg/L, which was almost equal to 3 and 27 times the concentration related to asphalt plant (40.08 μg/L) and paving site (4.08 μg/L), respectively. Considering the construction site, the quantity of VOCs was comprised between 2 and 4 times the amount generated in the asphalt laboratory. This study aimed to assess the VOCs concentration quantitatively during both production and pavement construction operations, and the latter stage represents the more relevant scenario for future investigations.

Atmospheric Volatile Organic Compounds (VOCs) in China: a Review

The purpose of this review is to summarize the current understandings of atmospheric VOC characteristics in China and put forward the methodological drawbacks of the VOC measurement that need to be resolved and the research gaps that need to be filled. Whereas in recent investigations in the North China Plain (NCP) a reduction (20–66%) in total VOC concentration is noticed compared with the ones published before 2015, an increase (13–127%) is observed for the Yangtze River Delta (YRD) region. Aromatics and oxygenated VOCs are frequently appearing as the most abundant VOC group in recent investigations. Industry-related VOC sources are more dominant in the YRD regions while vehicle-related sources are more influential in the NCP, Central China, and Pearl River Delta regions. Benzene, 1,3,5-trimethylbenzene, ethylbenzene, naphthalene, dichloromethane, 1,2-dichloroethane, 1,2-dichloropropane, chloroform, carbon tetrachloride, and 1,2-dibromoethane pose carcinogenic risk to exposed population in China and the most risk-prone areas are affected by the petrochemical industry, biomass burning, waste management, and vehicle emissions. Formaldehyde and toluene have relatively high concentrations among the different indoor VOCs observed and their concentrations noticed to be exceeded the national air quality standard. More investigations have to be performed on rarely studied health risk assessment of VOCs and characterization of indoor VOCs. BVOC studies are rarely conducted in China, which has to be performed on common plant species, different forest, and agricultural crops. VOC characterization in forest fire smokes and more process-specific emission characteristics in common industries need to be conducted.

An exploratory study on online quantification of isoprene in human breath using cavity ringdown spectroscopy in the ultraviolet

Breath analysis offers a promising method of noninvasive analyses of volatile metabolites and xenobiotics present in human body. Isoprene is one of the highest abundant volatile organic compounds (VOCs) present in human exhaled breath. Breath isoprene (50–200 part per billion by volume (ppbv) or higher) can be analyzed by using mass spectroscopy-based methods, yet laser absorption spectral detection of breath isoprene has not been much reported, partially due to its ultraviolet (UV) absorption wavelength and the spectral overlap with other breath VOCs such as acetone in the same wavelength region. These facts make it challenging to develop a spectroscopy-based breath isoprene analyzer for a potential portable instrument. Here we report on the development of a cavity ringdown spectroscopy (CRDS) system for detection of breath isoprene in the UV region near 226 nm. First, we investigated spectral absorption interferences near 226 nm and selected an optimal detection wavelength at 226.56 nm with minimum to no spectral interference. We then measured absorption cross-sections of isoprene at 225.5–227.4 nm under controlled cavity pressures, and the measured absorption cross-section 1.93 × 10−17 cm2/molecule at 226.56 nm was used to quantify isoprene in different cases including human breath gas samples. Finally, we validated the CRDS system by measuring breath gas samples from 19 human subjects using proton transfer reaction mass spectrometry (PTR-MS). The CRDS system shows good linear response (R2 = 0.999), high stability (0.2%), and high accuracy (R2 = 0.906 with PTR-MS). The limit of detection of the system was 0.47 ppbv, with average over 100 ringdown events (equivalent to 5 s). This work represents the first exploratory study of the detection of breath isoprene using CRDS. The results demonstrate the potential of developing a CRDS-based breath analyzer for online, near-real time, sensitive analysis of breath isoprene for further research that would help to elucidate its physiological and clinical significance.

Isoprene flux from permeable carbonate sediments on the Great Barrier Reef

Isoprene is the most abundant biogenic volatile organic compound (BVOC) on the planet, with annual emissions accounting for up to half of all BVOC emissions. Isoprene has been measured extensively in terrestrial habitats where it is highly abundant; however, there is limited knowledge on marine systems where it is found at lower concentrations. Here, we report for the first time isoprene fluxes from coral reef permeable carbonate sediments with a cover of microphytobenthos (MPB) from Heron and Lizard Islands, on the southern and northern ends of the Great Barrier Reef, respectively. Using advective and diffusive benthic chambers, we measured isoprene fluxes over full diel cycles on both islands. Net effluxes of isoprene from the sediment to the water column were observed at both Heron Island (mean: 10.0 ± 1.1 nmol m2 h−1) and Lizard Island (mean: 3.9 ± 0.9 nmol m2 h−1). Light isoprene fluxes were much higher on Heron Island than on Lizard Island and both islands had lower isoprene emissions in the dark. Higher isoprene fluxes during the day reflects the role of MPB photosynthesis in isoprene production. Lower isoprene fluxes at night is most likely due to isoprene consumption by microbial activity or less production in the absence of photosynthesis. The contribution of benthic isoprene emissions from coral reef carbonate sands worldwide (0.52 Gg C y−1) were estimated to represent less than 0.005% of the global marine atmospheric fluxes (11,600 Gg C y−1).

Observation and analysis of VOCs in nine prefecture-level cities of Sichuan Province, China.

The observation and analysis of volatile organic compounds (VOCs) were conducted during January 2018 in nine prefecture-level cities of Sichuan, China, covering the period of heavily polluted weather. Air samples collected in nine prefecture-level cities were analyzed using a preconcentration method coupled with GC-MS/FID. The characteristics and ozone generation potential (OFP) of VOCs were analyzed. The relationship between air quality index (AQI) and VOCs and gross domestic product (GDP) and VOCs were also discussed, respectively. The results show that the characteristics of VOCs in cities are highly related to their industrial structure and GDP. Generally, areas with high AQI values are accompanied by high VOC concentrations. Alkanes and halocarbons were the most abundant VOCs in the atmospheric environment in the nine prefecture-level cities, accounting for 24.5~61.6% and 15.6~23.6% of total VOC concentration, respectively. The MIR method was used to analyze the OFP, and olefins contributed the most to ozone formation. Among the nine cities located in Sichuan, Dazhou was found to be the city with the highest OFP value (1191.49μg/m3).

Identification of isoprene-degrading bacteria in phyllosphere and soil communities from high isoprene-emitting oil palm trees by DNA-stable isotope probing

Isoprene is the most abundant biogenic volatile organic compound (BVOC) on Earth, with annual global emissions almost equal to those from methane. Due to its volatile nature and high reactivity, isoprene plays a complex role in atmospheric chemistry and hence, climate. However, very little is known about its biological degradation in the environment. The vast majority of isoprene (500 Tg ·y-1) is produced by terrestrial plants and oil palm is considered one of the highest isoprene-producing trees, with estimated emissions of 175 μg·g-1 dry leaves ·h-1. Oil palm is also a heavily cultivated crop since it is the source of 30% of the vegetable oil in the world and in countries such as Malaysia represents >85% of total agricultural land. The vast expansion of a single crop that emits such high amounts of isoprene have raised serious concerns about its impact on air quality and climate change. We performed DNA Stable Isotope Probing (DNA-SIP) to study the isoprene-degrading community of oil palm trees in a Malaysian plantation and identified novel genera of isoprene-utilising bacteria in both oil palm soils and leaves. isoA amplicon sequencing data also confirmed that oil palm trees harbour a novel diversity of isoA genes, which encode the alpha subunit of the isoprene monooxygenase, a key enzyme in isoprene metabolism. In addition, metagenome assembled genomes (MAGs) were reconstructed from metagenomes from oil palm soil and leaf incubations and analysed to identify isoprene degradation gene clusters in these microorganisms. Finally, analysis of unenriched metagenomes showed that isoA-containing bacteria are more abundant in soils than in the oil palm phyllosphere.

Molecular Ecology of Isoprene-Degrading Bacteria.

Isoprene is a highly abundant biogenic volatile organic compound (BVOC) that is emitted to the atmosphere in amounts approximating to those of methane. The effects that isoprene has on Earth’s climate are both significant and complex, however, unlike methane, very little is known about the biological degradation of this environmentally important trace gas. Here, we review the mechanisms by which bacteria catabolise isoprene, what is known about the diversity of isoprene degraders in the environment, and the molecular tools currently available to study their ecology. Specifically, we focus on the use of probes based on the gene encoding the α-subunit of isoprene monooxygenase, isoA, and DNA stable-isotope probing (DNA-SIP) alone or in combination with other cultivation-independent techniques to determine the abundance, diversity, and activity of isoprene degraders in the environment. These parameters are essential in order to evaluate how microbes might mitigate the effects of this important but neglected climate-active gas. We also suggest key aspects of isoprene metabolism that require further investigation in order to better understand the global isoprene biogeochemical cycle.

Molecular Cloning and Functional Characterization of CpMYC2 and CpBHLH13 Transcription Factors from Wintersweet (Chimonanthus praecox L.).

Wintersweet (Chimonanthus praecox L.) is an ornamental and economically significant shrub known for its unique flowering characteristics, especially the emission of abundant floral volatile organic compounds. Thus, an understanding of the molecular mechanism of the production of these compounds is necessary to create new breeds with high volatile production. In this study, two bHLH transcription factors (CpMYC2 and CpbHLH13) of Wintersweet H29 were functionally characterized to illustrate their possible role in the production of volatile compounds. The qRT-PCR results showed that the expression of CpMYC2 and CpbHLH13 increased from the flower budding to full bloom stage, indicating that these two genes may play an essential role in blooming and aroma production in wintersweet. Gas chromatography-mass spectroscopy (GC-MS) analysis revealed that the overexpression of CpMYC2 in arabidopsis (Arabidopsis thaliana) AtMYC2-2 mutant (Salk_083483) and tobacco (Nicotiana tabaccum) genotype Petit Havana SR1 significantly increased floral volatile monoterpene, especially linalool, while the overexpression of CpbHLH13 in Arabidopsis thaliana ecotype Columbia-0 (Col-0) and tobacco genotype SR1 increased floral sesquiterpene β-caryophyllene production in both types of transgenic plants respectively. High expression of terpene synthase (TPS) genes in transgenic A. thaliana along with high expression of CpMYC2 and CpbHLH13 in transgenic plants was also observed. The application of a combination of methyl jasmonic acid (MeJA) and gibberellic acid (GA3) showed an increment in linalool production in CpMYC2-overexpressing arabidopsis plants, and the high transcript level of TPS genes also suggested the involvement of CpMYC2 in the jasmonic acid (JA) signaling pathway. These results indicate that both the CpMYC2 and CpbHLH13 transcription factors of wintersweet are possibly involved in the positive regulation and biosynthesis of monoterpene (linalool) and sesquiterpene (β-caryophyllene) in transgenic plants. This study also indicates the potential application of wintersweet as a valuable genomic material for the genetic modification of floral scent in other flowering plants that produce less volatile compounds.

Observation-Based Modeling of O3–Precursor Relationships in Nanjing, China

Surface ozone (O3) is formed through a series of photochemical reactions of nitrogen oxides (NOx) and volatile organic compounds (VOCs) in the atmosphere. In recent years, ozone concentrations in Nanjing have been increasing. To effectively mitigate ozone pollution, it is essential to understand the relationship between O3 and its precursors. In this study, the observation-based model (OBM) coupled with the Master Chemical Mechanism (MCM), was applied to investigate the O3-NOx-VOCs relationship in the Nanjing Metropolitan Area of China in summer 2015. The OBM model well reproduces the levels and diurnal variations of O3 with a high index of agreement value. Analysis of ozone formation potential (OFP) indicates that although observed alkanes are the most abundant VOCs (46.8%), their contributions to OFP are relatively small due to lower maximum incremental reactivity (MIR). Aromatics contribute the most to OFP (61.6%), followed by alkenes (18%). These two groups dominate in the top ten VOCs of OFP. In particular, m/p-Xylene shows a significant contribution to OFP with the highest OFP value over 30 µg/m3. The relative incremental reactivity (RIR) results demonstrate that the reduction of anthropogenic VOCs (AVOCs) is the most efficient way to mitigate local O3 pollution in Nanjing. Specifically, m/p-Xylene emissions should be reduced at it shows the highest RIR among all the AVOCs. Based on the results of OBM, a cutting ratio of AVOCs to NOx of more than 0.46 is proposed to implement efficient control measurements in Nanjing for the study period.

Unraveling Conformer-Specific Sources of Hydroxyl Radical Production from an Isoprene-Derived Criegee Intermediate by Deuteration.

Ozonolysis of isoprene, the most abundant volatile organic compounds emitted into the Earth's troposphere after methane, yields three distinct Criegee intermediates. Among these, methyl vinyl ketone oxide (MVK-oxide) is predicted to be the major source of atmospheric hydroxyl radicals (OH) from isoprene ozonolysis. Previously, Barber et al. [ J. Am. Chem. Soc., 2018, 140, pp 10866-10880] demonstrated that syn-MVK-oxide conformers undergo unimolecular decay via 1,4-hydrogen (H) transfer from the methyl group to the adjacent terminal oxygen atom, followed by the prompt release of OH radical products. Here, we selectively deuterate the methyl group of MVK-oxide (d3-MVK-oxide) and record its IR action spectrum in the vinyl CH stretch overtone (2νCH) region. The resultant time-dependent appearance of OD radical products, detected by laser-induced fluorescence, demonstrates that a unimolecular decay of d3-MVK-oxide proceeds by an analogous 1,4-deuterium (D) atom transfer mechanism anticipated for syn conformers. The experimental spectral and temporal results are compared with the calculated IR absorption spectrum and unimolecular decay rates predicted by the Rice-Ramsperger-Kassel-Marcus (RRKM) theory for syn-d3-MVK-oxide, as well as the prior study on syn-MVK-oxide. The d3-MVK-oxide IR action spectrum is similar to that for MVK-oxide, yet exhibits notable changes as the overtone and combination transitions involving CD stretch shift to a lower frequency. The unimolecular decay rate for d3-MVK-oxide is predicted to be a factor of 40 times slower than that for MVK-oxide in the 2νCH region. Experimentally, the temporal profile of the OD products reflects the slower unimolecular decay of d3-MVK-oxide compared to that for MVK-oxide to OH products as well as experimental factors. Both experiment and theory demonstrate that quantum mechanical tunneling plays a very important role in the 1,4-H/D-transfer processes at energies in the vicinity of the transition-state barrier. The similarities of the IR action spectra and changes in the unimolecular decay dynamics upon deuteration indicate that syn conformers make the main contribution to the IR action spectra of MVK-oxide and d3-MVK-oxide.

Quantifying source contributions of volatile organic compounds under hydraulic fracking moratorium

Volatile organic compounds (VOCs) are precursors for ozone (O3) and secondary particulate matter, which contribute to asthma and cardiovascular diseases. With the technology development of hydraulic fracking, the United States experienced a shale gas boom in the last decade while the public raised concerns about the potential health impacts of co-emitted VOCs and other airborne pollutants. National Energy Technology Laboratory conducted stationary trailer-based ambient monitoring to study the sources of VOCs in Maryland, where the state enacted a moratorium on unconventional natural gas extraction. The campaign had two periods, May to August 2014 (summer) and November 2014 to February 2015 (winter). Ethane was the most abundant VOC, averaging 12.3 ppb (SD = 15.7 ppb) in summer and 21.7 ppb (SD = 21.6 ppb) in winter. The seasonal variation of VOCs indicated different source strengths. The sampling region was in the nitrogen oxides (NOx) limited regime for O3 production, and the O3 concentrations were sensitive to VOC/NOx ratios in the early mornings. We derived a six-factor profile using positive matrix factorization: motor vehicles, industrial, biogenics, coal burning, fugitive and evaporative, and ozone secondary. The fugitive and evaporative factor explained 44.5% of total VOCs, and the motor vehicles factor followed second with 15.5%. Oil and gas activities had a considerable impact on the abundance of VOCs in this region.

Occurrence, Probable Source, and Health Risk Assessment of Benzene, Toluene, Ethylbenzene, and Xylene Compounds in Ambient Urban Atmosphere in Ahvaz, Iran

Background & Aims of the StudyThe benzene, toluene, ethylbenzene, and xylene (BTEX) compounds are the most abundant volatile organic compounds in the urban atmosphere. This study aimed to investigate and monitor the ambient BTEX compounds in Ahvaz, Iran.Materials and MethodsThe atmospheric concentrations of the BTEX were measured using the Air Quality Monitoring Station in the center of Ahvaz. Hourly mean concentration data of the BTEX compounds from March 21, 2017, until November 21, 2017, were obtained from the environmental protection organization of Khuzestan province.ResultsMean concentrations of the BTEX compounds were 0.80±0.04, 2.55±0.10, 0.54±0.03, and 1.26±0.07 µg/m3, respectively, and these concentrations were lower in the summer, compared to other seasons. A significant relationship between benzene and other BTEX compounds indicates that BTEX release from certain sources, such as gasoline vehicles. Moreover, the mean toluene/benzene ratio was estimated at 3.29±0.84, and this ratio shows that the highest concentrations of pollutant emissions were emitted from the activity traffic. Carcinogen risk assessment of Ahvazi people exposure to benzene showed that the mean cancer risk value for benzene exposure was 0.89×10−6, which was lower than the unit cancer risk value (i.e., 1×10-6). Hazard quotient's calculation showed that the mean non-carcinogenic risk values for exposure to BTEX compounds were 3.84, 0.074, 0.077, and 1.76, respectively. The mean hazard index (HI) for exposure to BTEX compounds was 5.75, which was considerably higher than the unit value of 1.ConclusionBased on the findings, the necessity of controlling BTEX emissions, especially benzene and identifying the sources of these compounds can be a useful tool for the management of connected control strategies.

Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates.

Ozonolysis of isoprene, one of the most abundant volatile organic compounds emitted into the Earth's atmosphere, generates two four-carbon unsaturated Criegee intermediates, methyl vinyl ketone oxide (MVK-oxide) and methacrolein oxide (MACR-oxide). The extended conjugation between the vinyl substituent and carbonyl oxide groups of these Criegee intermediates facilitates rapid electrocyclic ring closures that form five-membered cyclic peroxides, known as dioxoles. This study reports the first experimental evidence of this novel decay pathway, which is predicted to be the dominant atmospheric sink for specific conformational forms of MVK-oxide (anti) and MACR-oxide (syn) with the vinyl substituent adjacent to the terminal O atom. The resulting dioxoles are predicted to undergo rapid unimolecular decay to oxygenated hydrocarbon radical products, including acetyl, vinoxy, formyl, and 2-methylvinoxy radicals. In the presence of O2, these radicals rapidly react to form peroxy radicals (ROO), which quickly decay via carbon-centered radical intermediates (QOOH) to stable carbonyl products that were identified in this work. The carbonyl products were detected under thermal conditions (298 K, 10 Torr He) using multiplexed photoionization mass spectrometry (MPIMS). The main products (and associated relative abundances) originating from unimolecular decay of anti-MVK-oxide and subsequent reaction with O2 are formaldehyde (88 ± 5%), ketene (9 ± 1%), and glyoxal (3 ± 1%). Those identified from the unimolecular decay of syn-MACR-oxide and subsequent reaction with O2 are acetaldehyde (37 ± 7%), vinyl alcohol (9 ± 1%), methylketene (2 ± 1%), and acrolein (52 ± 5%). In addition to the stable carbonyl products, the secondary peroxy chemistry also generates OH or HO2 radical coproducts.

Impact of plants on the diversity and activity of methylotrophs in soil

BackgroundMethanol is the second most abundant volatile organic compound in the atmosphere, with the majority produced as a metabolic by-product during plant growth. There is a large disparity between the estimated amount of methanol produced by plants and the amount which escapes to the atmosphere. This may be due to utilisation of methanol by plant-associated methanol-consuming bacteria (methylotrophs). The use of molecular probes has previously been effective in characterising the diversity of methylotrophs within the environment. Here, we developed and applied molecular probes in combination with stable isotope probing to identify the diversity, abundance and activity of methylotrophs in bulk and in plant-associated soils.ResultsApplication of probes for methanol dehydrogenase genes (mxaF, xoxF, mdh2) in bulk and plant-associated soils revealed high levels of diversity of methylotrophic bacteria within the bulk soil, including Hyphomicrobium, Methylobacterium and members of the Comamonadaceae. The community of methylotrophic bacteria captured by this sequencing approach changed following plant growth. This shift in methylotrophic diversity was corroborated by identification of the active methylotrophs present in the soils by DNA stable isotope probing using 13C-labelled methanol. Sequencing of the 16S rRNA genes and construction of metagenomes from the 13C-labelled DNA revealed members of the Methylophilaceae as highly abundant and active in all soils examined. There was greater diversity of active members of the Methylophilaceae and Comamonadaceae and of the genus Methylobacterium in plant-associated soils compared to the bulk soil. Incubating growing pea plants in a 13CO2 atmosphere revealed that several genera of methylotrophs, as well as heterotrophic genera within the Actinomycetales, assimilated plant exudates in the pea rhizosphere.ConclusionIn this study, we show that plant growth has a major impact on both the diversity and the activity of methanol-utilising methylotrophs in the soil environment, and thus, the study contributes significantly to efforts to balance the terrestrial methanol and carbon cycle.48Q8VLgPYzztrQXqtA_fDqVideo abstract