Browsing by Author "McGlynn, Deborah"

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  • Portable, low-cost samplers for distributed sampling of atmospheric gases
    Hurley, James; Caceres, Alejandra; McGlynn, Deborah; Tovillo, Mary; Pinar, Suzanne; Schuerch, Roger; Onufrieva, Ksenia; Isaacman-VanWertz, Gabriel (2023-10-13)
    Volatile organic compounds (VOCs) contribute to air pollution both directly, as hazardous gases, and through their reactions with common atmospheric oxidants to produce ozone, particulate matter, and other hazardous air pollutants. There are enormous ranges of structures and reaction rates among VOCs, and consequently a need to accurately characterize the spatial and temporal distribution of individual identified compounds. Current VOC measurements are often made with complex, expensive instrumentation that provides high chemical detail, but is limited in its portability and requires high expense (e.g., mobile labs) for spatially resolved measurements. Alternatively, periodic collection of samples on cartridges is inexpensive but demands significant operator interaction that can limit possibilities for time-resolved measurements or distributed measurements across a spatial area. Thus, there is a need for simple, portable devices that can sample with limited operator presence to enable temporally and/or spatially resolved measurements. In this work, we describe new portable and programmable VOC samplers that enable simultaneous collection of samples across a spatially distributed network, validate their reproducibility, and demonstrate their utility. Validation experiments confirmed high precision between samplers as well as the ability of miniature ozone scrubbers to preserve reactive analytes collected on commercially available adsorbent gas sampling cartridges, supporting simultaneous field deployment across multiple locations. In indoor environments, 24-hour integrated samples demonstrate observable day-to-day variability, as well as variability across very short spatial scales (meters). The utility of the samplers was further demonstrated by locating outdoor point sources of analytes through the development of a new mapping approach that employs a group of the portable samplers and back projection techniques to assess a sampling area with higher resolution than stationary sampling. As with all gas sampling, the limits of detection depend on sampling times and the properties of sorbent and analyte. Limit of detection of the analytical system used in this work is on the order of nanograms, corresponding to mixing ratios of 1-10 pptv after one hour of sampling at the programmable flow rate of 50-250 sccm enabled by the developed system. The portable VOC samplers described and validated here provide a simple, low-cost sampling solution for spatially and/or temporally variable measurements of any organic gases that are collectable on currently available sampling media.
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    Understanding Long-Term Variations in Surface Ozone in United States (U.S.) National Parks
    McGlynn, Deborah; Mao, Huiting; Wu, Zhaohua; Sive, Barkley; Sharac, Timothy (MDPI, 2018-03-25)
    Long-term surface ozone observations at 25 National Park Service sites across the United States were analyzed for processes on varying time scales using a time scale decomposition technique, the Ensemble Empirical Mode Decomposition (EEMD). Time scales of interest include the seasonal cycle, large-scale climate oscillations, and long-term (>10 years) trends. Emission reductions were found to have a greater impact on sites that are nearest major urban areas. Multidecadal trends in surface ozone were increasing at a rate of 0.07 to 0.37 ppbv year−1 before 2004 and decreasing at a rate of −0.08 to −0.60 ppbv year−1 after 2004 for sites in the East, Southern California, and Northwestern Washington. Sites in the Intermountain West did not experience a reversal of trends from positive to negative until the mid- to late 2000s. The magnitude of the annual amplitude (=annual maximum–minimum) decreased at eight sites, two in the West, two in the Intermountain West, and four in the East, by 5–20 ppbv and significantly increased at three sites; one in Alaska, one in the West, and one in the Intermountain West, by 3–4 ppbv. Stronger decreases in the annual amplitude occurred at a greater proportion of sites in the East (4/6 sites) than in the West/Intermountain West (4/19 sites). The date of annual maximums and/or minimums has changed at 12 sites, occurring 10–60 days earlier in the year. There appeared to be a link between the timing of the annual maximum and the decrease in the annual amplitude, which was hypothesized to be related to a decrease in ozone titration resulting from NOx emission reductions. Furthermore, it was found that a phase shift of the Pacific Decadal Oscillation (PDO), from positive to negative, in 1998–1999 resulted in increased occurrences of La Niña-like conditions. This shift had the effect of directing more polluted air masses from East Asia to higher latitudes over the North American continent. The change in the Pacific Decadal Oscillation (PDO)/El Niño Southern Oscillation (ENSO) regime influenced surface ozone at an Alaskan site over its nearly 30-year data record.