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Pesticides registered with the U.S. EPA for mosquito control are called adulticides and are released directly into the atmosphere as aerosols to target flying mosquitos. This adulticide application approach is different from traditional (agricultural) pesticide applications, yet the fate and transport of adulticides in large metropolitan areas is largely unknown. The Houston Metropolitan Area encompasses eight counties, many of which require county-level mosquito control programs that utilize adulticides. Malathion and permethrin are the primary adulticides used by Harris County (HC) in Houston, TX, USA. Houston, like many other metropolitan areas, has an urban atmosphere supporting the oxidation of both gas and particle phase pollutants. During the summer mosquito season of 2016, we collected atmospheric total suspended particulate matter (PM) samples at Jones Forest (JF), located in Montgomery County (directly north of HC) to investigate the atmospheric transport and oxidation of adulticides in an urban atmosphere. Despite HC alternating the adulticide treatment schedule, we measured permethrin, malathion, and malaoxon (oxidation product of malathion), throughout the sampling campaign. These consistent measurements, in conjunction with 12 h backward trajectories, support the conclusion that JF is influenced by other county-level mosquito-control programs and agricultural pesticide use. This cross-county transport may impact adulticide effectiveness by supporting pesticide resistance in mosquito populations due to repeated exposures to pesticides. This study highlights the need for mosquito control collaborations between counties, especially in areas of urban expansion overlapping with agricultural activities.

Changing urban emission landscapes and increasing population make it imperative to understand the driving forces for air quality in growing urban areas. Recent field studies in an industrial area in Houston and a semiurban area in San Antonio reveal unique emission signatures for these two growing Texas cities. A comparison of benzene, toluene, xylenes, isoprene, and methyl ethyl ketone (MEK) was conducted for these two Texas locations and previous studies in other megacities. It was found that San Antonio had similar emission ratios as these megacities for benzene, toluene, and xylenes (1.10, 4.57, and 3.60 pptv ppbv−1 of CO, respectively), likely indicating a similar traffic emission source. Isoprene and MEK were of biogenic origin in San Antonio. However, analysis of emission ratios, diurnal trends, and comparison with emission inventories indicated that benzene, toluene, and MEK were likely associated with fugitive and stack emissions in the industrial corridor in Houston. Isoprene in Houston appeared to have mixed fugitive and biogenic sources in Houston, based on diurnal trends and emission ratio. The peak nighttime concentrations for benzene, toluene, xylene, isoprene, and MEK observed during the campaign were 66, 533, 21, 138, and 731 ppbv, respectively, in the Houston site. The emission ratio for xylenes (3.37 pptv ppbv−1 of CO) for the Houston site was similar to Paris, London, and Mexico City, despite emission inventories indicating high fugitive and stack emissions. The conditional probability function (CPF) analysis closely matched the direction of the industrial sources with the highest recorded emission levels as listed in the emission inventory for the Houston site. The estimated ozone production efficiency (OPE) for the industrial area in Houston indicated volatile organic compound (VOC)–limited conditions in the morning, which transitioned to nitrogen oxide (NOx)–limited conditions in the afternoon. Texas cities have complex emission scenarios, and future efforts to mitigate ozone and particulate matter may have to consider a variety of emission reduction strategies.

Current in vitro studies do not typically assess cellular impacts in relation to real-world atmospheric mixtures of gases. In this study, we set out to examine the feasibility of measuring biological responses at the level of gene expression in human lung cells upon direct exposures to air in the field. This study describes the successful deployment of lung cells in the heavily industrialized Houston Ship Channel. By examining messenger RNA (mRNA) levels from exposed lung cells, we identified changes in genes that play a role as inflammatory responders in the cell. The results show anticipated responses from negative and positive controls, confirming the integrity of the experimental protocol and the successful deployment of the in vitro instrument. Furthermore, exposures to ambient conditions displayed robust changes in gene expression. These results demonstrate a methodology that can produce gas-phase toxicity data in the field.

Situated at a land-sea interface, Houston, Texas, is a national hub for the petrochemical industry and has the second fastest-growing metropolitan population in the United States. Addressing air quality in this region is uniquely challenging, due in part to its wide range of meteorological conditions (e.g. , convection systems and temperature inversions) and continuum of volatile organic compound (VOC) and aerosol sources (e.g. , anthropogenic and biogenic). As a result, Houston was chosen as the location for the Department of Energy's Atmospheric Radiation Measurement (ARM) program-led Tracking Aerosol Convection ExpeRiment (TRACER), which investigated cloud and aerosol interactions in the deep convection over the area. Deployed as a key asset, ARM's tethered balloon system (TBS) was used to investigate questions related to the vertical distributions of aerosols and their formation, including their precursor species volatile organic compounds. Platforms like TBSs and uncrewed aerial vehicles (UAVs) can bridge the vertical gap between ground-based and crewed airplane measurement platforms to focus on near-surface characterization. However, there has been limited effort to modularize and integrate VOC samplers into instrument payloads on both aerial systems. In this study, lightweight and robust VOC samplers were designed and deployed on the TBS and a UAV to collect VOCs in flight. The modular design allowed for scalable adjustments to meet the unique platform requirements and enabled multiple flights per sampling day. Each sampler can autonomously collect VOCs on up to four sorbent tubes for subsequent thermal desorption-gas chromatography-mass spectrometry analysis. The low sampler mass (2.2 kg and 800 g, TBS and UAV, respectively) enables the combination of these VOC samplers with trace gas, aerosol, and meteorological sensors on aerial platforms. These profiles allow us to assess temporal changes in VOC magnitude and composition at multiple locations. Observations from TBS and UAV flights during TRACER are presented and future considerations for sampler design and deployments are discussed. [ABSTRACT FROM AUTHOR]

As criteria pollutants from anthropogenic emissions have declined in the US in the last two decades, biomass burning (BB) emissions are becoming more important for urban air quality. Tracking the transported BB emissions and their impacts is challenging, especially in areas that are also burdened by anthropogenic sources like the Texas Gulf coast. During the Corpus Christi and San Antonio (CCSA) field campaign in Spring 2021, two long-range transport BB events (BB1 and BB2) were identified. The observed patterns of absorption Ångström Exponent (AAE), high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) BB tracer (f60), equivalent black carbon (eBC), acetonitrile and carbon monoxide (CO) during BB1 and BB2 indicated differences in the mixing of transported BB plumes with local anthropogenic sources. The combined information from HYSPLIT backward trajectory (BTs) and satellite observations revealed that BB1 had mixed influence of transported smoke plumes from fires in Central Mexico, the Yucatan peninsula, and the Central US, whereas BB2 was influenced majorly by fires in the Central US. The estimated transport time of smoke from the Mexican fires and the Central US fires to our study site were not too different (48–54 hours and 24–36 hours, respectively) and both events appeared to have undergone similar levels of atmospheric processing, as evident in the elemental ratios of bulk organic aerosol (OA). We observed a progression of f44 vs. f60 as a function of time elapsed during BB2. Positive matrix factorization (PMF) analysis of OA showed that BB1 had a mixture of organics from aged BB emission with an anthropogenic marine signal while the oxidized organic compounds from aged BB emissions dominated the aerosols during BB2. While aerosol measurements exhibited good agreement with respect to the BB designation, the CO and acetonitrile trends revealed more complicated source contributions. Our analysis from mobile and stationary measurements highlights that both CO and acetonitrile are likely impacted by local sources even during the BB events and specifically that acetonitrile cannot be used as a unique BB tracer for dilute BB plumes in an industrially influenced location. Finally, we provide evidence of the potential regional impacts of these transported BB events on urban O3 levels using measurements from the surface air quality monitoring network in Texas. [ABSTRACT FROM AUTHOR]