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Oil sands are a prominent unconventional source of petroleum. Total organic carbon measurements via an aircraft campaign (Spring-Summer 2018) revealed emissions above Canadian oil sands exceeding reported values by 1900-6300%. The “missing” compounds were predominantly intermediate- and semi-volatile organic compounds, which are prolific precursors to secondary organic aerosol formation. Here we use a novel combination of aircraft-based measurements (including total carbon emissions measurements) and offline analytical instrumentation to characterize the mixtures of organic carbon and their volatility distributions above oil sands facilities. These airborne, real-time observations are supplemented by laboratory experiments identifying substantial, unintended emissions from waste management practices, emphasizing the importance of accurate facility-wide emissions monitoring and total carbon measurements to detect potentially vast missing emissions across sources.Detailed chemical speciation confirms these observations near both surface mining and in-situ facilities were oil sands-derived, with facility-wide emissions around 1% of extracted petroleum—a comparable loss rate to natural gas extraction. Total emissions, spanning extraction through waste processing, were equivalent to total Canadian anthropogenic emissions from all sources. These results demonstrate that the full air quality and environmental impacts of oil sands operations cannot be captured without complete coverage of a wider volatility range of emissions.

Volatile chemical products (VCPs) and other non-combustion-related sources have become important for urban air quality, and bottom-up calculations report emissions of a variety of functionalized compounds that remain understudied and uncertain in emissions estimates. Using a new instrumental configuration, we present online measurements of oxygenated organic compounds in a US megacity over a 10 d wintertime sampling period, when biogenic sources and photochemistry were less active. Measurements were conducted at a rooftop observatory in upper Manhattan, New York City, USA using a Vocus chemical ionization time-of-flight mass spectrometer, with ammonium (NH4+) as the reagent ion operating at 1 Hz. The range of observations spanned volatile, intermediate-volatility, and semi-volatile organic compounds, with targeted analyses of ∼150 ions, whose likely assignments included a range of functionalized compound classes such as glycols, glycol ethers, acetates, acids, alcohols, acrylates, esters, ethanolamines, and ketones that are found in various consumer, commercial, and industrial products. Their concentrations varied as a function of wind direction, with enhancements over the highly populated areas of the Bronx, Manhattan, and parts of New Jersey, and included abundant concentrations of acetates, acrylates, ethylene glycol, and other commonly used oxygenated compounds. The results provide top-down constraints on wintertime emissions of these oxygenated and functionalized compounds, with ratios to common anthropogenic marker compounds and comparisons of their relative abundances to two regionally resolved emissions inventories used in urban air quality models.

To help tackle drought-related farmer suicides, a new design of a rain simulator, recently patented is presented (Patent no. 351688, Govt. of India Patent Office). This is versatile and yields show...

Laboratory and field observations of organic compound emissions reveal a previously unknown source of reactive pollution precursors., Asphalt-based materials are abundant and a major nontraditional source of reactive organic compounds in urban areas, but their emissions are essentially absent from inventories. At typical temperature and solar conditions simulating different life cycle stages (i.e., storage, paving, and use), common road and roofing asphalts produced complex mixtures of organic compounds, including hazardous pollutants. Chemically speciated emission factors using high-resolution mass spectrometry reveal considerable oxygen and reduced sulfur content and the predominance of aromatic (~30%) and intermediate/semivolatile organic compounds (~85%), which together produce high overall secondary organic aerosol (SOA) yields. Emissions rose markedly with moderate solar exposure (e.g., 300% for road asphalt) with greater SOA yields and sustained SOA production. On urban scales, annual estimates of asphalt-related SOA precursor emissions exceed those from motor vehicles and substantially increase existing estimates from noncombustion sources. Yet, their emissions and impacts will be concentrated during the hottest, sunniest periods with greater photochemical activity and SOA production.

The molecular-level composition and structure of organic aerosol (OA) affect its chemical/physical properties, transformations, and impacts. Here, we use the molecular-level chemical composition of functionalized OA from three diverse field sites to evaluate the effect of molecular-level compositional variability on OA phase state and thermodynamic mixing favorability. For these ambient sites, modeled aerosol phase state ranges from liquid to semisolid. The observed variability in OA composition has some effect on resulting phase state, but other factors like the presence of inorganic ions, aerosol liquid water, and internal versus external mixing with water are determining factors in whether these particles exist as liquids, semisolids, or solids. Organic molecular composition plays a more important role in determining phase state for phase-separated (verus well-mixed) systems. Similarly, despite the observed OA compositional differences, the thermodynamic mixing favorability for OA samples with aerosol liquid water, isoprene oxidation products, or monoterpene oxidation products remains fairly consistent within each campaign. Mixing of filter-sampled OA and isoprene or monoterpene oxidation products is often favorable in both seasons, while mixing with water is generally unfavorable.

Complex airborne mixtures of organic compounds can contain 10,000′s of diverse compounds at trace concentrations. Here, we incorporate high-resolution mass spectrometry into our integrated offline sampling-to-analysis measurement system for routine molecular-level speciation of complex mixtures in gas- or particle-phase samples with detection limits of 2–20 pg L−1 (i.e. 0.2–1.9 ppt in 6 L samples). Analytes desorbed from custom adsorbent tubes (or filter extracts) were separated via gas chromatography (GC) and simultaneously analyzed by an electron ionization quadrupole mass spectrometer (EI-MS), and by atmospheric pressure chemical ionization (APCI) combined with a high-resolution quadrupole time-of-flight mass spectrometer (Q-TOF) with a resolution of 25,000–40,000 M/ΔM in HR-TOF and MS/MS modes. We demonstrated our system with simple standards, a Macondo crude oil standard as a reference for complex mixtures of common airborne compounds, and ambient samples using GC-TOF and GC–MS/MS. We speciated complex mixtures at mass accuracy error (i.e. mass tolerance) down to 8 ± 2 ppm (e.g. resolving analytes of mass 270.000 u with 0.003 u accuracy) using a targeted approach with 3000 molecular formulas, including hydrocarbons and functionalized analytes containing oxygen, sulfur, nitrogen, or phosphorous. This extended from compounds with 10 to 32 carbon atoms and up to 16 hydrocarbon formulas per carbon number, and a similar range for functionalized compound classes. We also demonstrated our MS/MS capabilities to differentiate structural isomers and determine the presence of specific functional groups; and our direct-TOF capability, which bypasses high-temperature chromatographic separation to preserve functionalized analytes.

The atmospheric evolution of organic compounds encompasses many thousands of compounds with varying volatility, polarity, and water solubility. The molecular-level chemical composition of this mixture plays a major, yet uncertain, role in its transformations and impacts. Here we perform a non-targeted molecular-level intercomparison of functionalized organic aerosol from three diverse field sites and a chamber. Despite similar bulk composition, we report large molecular-level variability between multi-hour organic aerosol samples at each site, with 66 ± 13% of functionalized compounds differing between consecutive samples. Single precursor environmental laboratory chamber experiments and fully chemically-explicit modeling confirm this variability is due to changes in emitted precursors, chemical age, and/or oxidation conditions. These molecular-level results demonstrate greater compositional variability than is typically observed in less-speciated measurements, such as bulk elemental composition, which tend to show less daily variability. These observations should inform future field and laboratory studies, including assessments of the effects of variability on aerosol properties and ultimately the development of strategic organic aerosol parameterizations for air quality and climate models. The detailed molecular-level speciation of organic aerosol is a highly challenging task. Here, the authors show an extensive molecular-level intercomparison of functionalized organic aerosol from three diverse field sites revealing large compositional variability between samples at each field site.

Gas-phase organic compounds across a range of volatilities, including volatile organic compounds (VOCs), are key components of outdoor air, indoor spaces, and a variety of other anthropogenic and biogenic systems. The collection of offline samples on adsorbent-packed tubes for analysis on laboratory instrumentation has been in use for decades, but with limited sensitivities and compound coverage. We present and evaluate our integrated sampling-to-analysis system that enables offline detailed chemical characterization of multi-faceted organic mixtures at trace concentrations. Its capabilities extend across a diverse variety of VOCs with different molecular features, as well as intermediate and semivolatile organic compounds (I/SVOCs). Samples can be collected manually or via automated devices that have been applied in chamber, field, and aircraft platforms. The laboratory instrumentation can be coupled to both a high resolution mass spectrometer (MS) and a traditional quadrupole MS, though performance metrics presented in this study are determined via the traditional MS. We demonstrate capabilities for detailed chemical characterization and routine performance for a wide range of compound functionalities at sub-part per trillion (ppt) concentrations, and as low as

This paper investigates the groundwater quality in six major districts of Madhya Pradesh in central India, namely, Balaghat, Chhindwara, Dhar, Jhabua, Mandla, and Seoni during the 2010-2011 sampling campaign, and discusses improvements made in the supplied water quality between the years 2011 and 2017. Groundwater is the main source of water for a combined rural population of over 7 million in these districts. Its contamination could have a huge impact on public health. We analyzed the data collected from a large-scale water sampling campaign carried out by the Public Health Engineering Department (PHED), Government of Madhya Pradesh between 2010 and 2011 during which all rural tube wells and dug wells were sampled in these six districts. Eight hundred thirty-one dug wells and 47,606 tube wells were sampled in total and were analyzed for turbidity, hardness, iron, nitrate, fluoride, chloride, and sulfate ion concentrations. Our study found water in 21 out of the 228 dug wells in Chhindwara district unfit for drinking due to fluoride contamination while all dug wells in Balaghat had fluoride within the permissible limit. Twenty-six of the 56 dug wells and 4825 of the 9390 tube wells in Dhar district exceeded the permissible limit for nitrate while 100% dug wells in Balaghat, Seoni, and Chhindwara had low levels of nitrate. Twenty-four of the 228 dug wells and 1669 of 6790 tube wells in Chhindwara had high iron concentration. The median pH value in both dug wells and tube wells varied between 6 and 8 in all six districts. Still, a significant number of tube wells exceeded a pH of 8.5 especially in Mandla and Seoni districts. In conclusion, this study shows that parts of inhabited rural Madhya Pradesh were potentially exposed to contaminated subsurface water during 2010-2011. The analysis has been correlated with rural health survey results wherever available to estimate the visible impact. We next highlight that the quality of drinking water has enormously improved since 2011 in all six districts as a result of rigorous treatment of extracted subsurface water on the ground before supplying to rural habitations as well as efficient distribution from healthy wells. Our research could provide impetus to the state government to develop innovative solutions for improving groundwater quality in these areas as existing solutions are largely protective techniques. We have identified specific ions responsible for groundwater contamination in different districts which would allow the development of district specific effective mitigation strategies.

Severe droughts were experienced by many southerly states of the Indian subcontinent during the past decade. Farmer suicides were reported from the state of Andhra Pradesh year after year, especially when the monsoons failed. The government of India conducted expensive rain enhancement experiments through artificial cloud seeding; this did happen, but at enormous infrastructural costs and organizational endeavors. In this paper, the attempt is to find alternative shower generation mechanisms at the scale of an individual cropland. The application of a new rain simulator is explored. The crux of the problem lies in generating showers with drops that not only fall with approximately the same speeds as the natural rain showers but also have matching drop size distributions. Previous simulators have not looked at this aspect; none have attempted to recreate a drop size spectrum that is indistinguishable from natural rain showers. This is the paper’s mainstay; new calculations are shown for a uniquely ...

UNLABELLED Particles are resuspended from the floor by walking and are subject to turbulent transport in the human aerodynamic wake. These processes may generate a vertical concentration gradient of particles. To estimate the magnitude of turbulence generated by walking, we measured the velocity field in the wake from floor to ceiling at 10-cm intervals with a sonic anemometer. The resulting eddy diffusion coefficients varied between 0.06 and 0.20 m(2) /s and were maximal at ~0.75-1 m above the floor, approximately the height of the swinging hand. We applied the eddy diffusion coefficients in an atmospheric transport model to predict concentrations of resuspended influenza virus as a function of the carrier particle size, height in the room, and relative humidity, which affects the resuspension rate coefficient and virus viability. Results indicated that the concentration of resuspended viruses at 1 m above the floor was up to 40% higher than at 2 m, depending on particle size. For exposure to total resuspended viruses, the difference at 1 vs. 2 m was 11-14%. It is possible that shorter people are exposed to higher concentrations of resuspended dust, including pathogens, although experimental evidence is needed to verify this proposition. PRACTICAL IMPLICATIONS Forces generated by walking can resuspend particles from the floor and create higher concentrations close to the floor and lower concentrations above it. These particles may include pathogens, such as the influenza virus, that were previously emitted into the air by an infected individual and that settled to the ground. Due to particle resuspension and turbulent transport, it is possible that shorter people are exposed to higher concentrations of particles, including certain pathogens, than are taller people. This work could be used in support of epidemiological investigations into the incidence of influenza as a function of a person’s height and to guide the design of more effective control strategies to reduce transmission of influenza.