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Featured researches published by Shelley Pressley.


Journal of Geophysical Research | 2006

Quantifying the seasonal and interannual variability of North American isoprene emissions using satellite observations of the formaldehyde column

Paul I. Palmer; Dorian S. Abbot; Tzung-May Fu; Daniel J. Jacob; Kelly Chance; Thomas P. Kurosu; Alex Guenther; Christine Wiedinmyer; Jenny Stanton; Michael J. Pilling; Shelley Pressley; Brian K. Lamb; Anna Louise Sumner

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. 111, D12315, doi:10.1029/2005JD006689, 2006 Quantifying the seasonal and interannual variability of North American isoprene emissions using satellite observations of the formaldehyde column Paul I. Palmer, 1,2 Dorian S. Abbot, 1 Tzung-May Fu, 1 Daniel J. Jacob, 1 Kelly Chance, 3 Thomas P. Kurosu, 3 Alex Guenther, 4 Christine Wiedinmyer, 4 Jenny C. Stanton, 5 Michael J. Pilling, 5 Shelley N. Pressley, 6 Brian Lamb, 6 and Anne Louise Sumner 7 Received 20 September 2005; revised 19 December 2005; accepted 14 February 2006; published 27 June 2006. [ 1 ] Quantifying isoprene emissions using satellite observations of the formaldehyde (HCHO) columns is subject to errors involving the column retrieval and the assumed relationship between HCHO columns and isoprene emissions, taken here from the GEOS- CHEM chemical transport model. Here we use a 6-year (1996–2001) HCHO column data set from the Global Ozone Monitoring Experiment (GOME) satellite instrument to (1) quantify these errors, (2) evaluate GOME-derived isoprene emissions with in situ flux measurements and a process-based emission inventory (Model of Emissions of Gases and Aerosols from Nature, MEGAN), and (3) investigate the factors driving the seasonal and interannual variability of North American isoprene emissions. The error in the GOME HCHO column retrieval is estimated to be 40%. We use the Master Chemical Mechanism (MCM) to quantify the time-dependent HCHO production from isoprene, a- and b-pinenes, and methylbutenol and show that only emissions of isoprene are detectable by GOME. The time-dependent HCHO yield from isoprene oxidation calculated by MCM is 20–30% larger than in GEOS-CHEM. GOME-derived isoprene fluxes track the observed seasonal variation of in situ measurements at a Michigan forest site with a 30% bias. The seasonal variation of North American isoprene emissions during 2001 inferred from GOME is similar to MEGAN, with GOME emissions typically 25% higher (lower) at the beginning (end) of the growing season. GOME and MEGAN both show a maximum over the southeastern United States, but they differ in the precise location. The observed interannual variability of this maximum is 20–30%, depending on month. The MEGAN isoprene emission dependence on surface air temperature explains 75% of the month-to-month variability in GOME-derived isoprene emissions over the southeastern United States during May–September 1996–2001. Citation: Palmer, P. I., et al. (2006), Quantifying the seasonal and interannual variability of North American isoprene emissions using satellite observations of the formaldehyde column, J. Geophys. Res., 111, D12315, doi:10.1029/2005JD006689. 1. Introduction [ 2 ] Emissions of volatile organic compounds (VOCs) from the terrestrial biosphere have important implications Division of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts, USA. Now at the School of Earth and Environment, University of Leeds, Leeds, UK. Harvard-Smithsonian Center for Astrophysics, Cambridge, Massachu- setts, USA. National Center for Atmospheric Research, Boulder, Colorado, USA. Department of Chemistry, University of Leeds, Leeds, UK. Department of Civil and Environmental Engineering, Washington State University, Pullman, Washington, USA. Battelle, Columbus, Ohio, USA. Copyright 2006 by the American Geophysical Union. 0148-0227/06/2005JD006689 for tropospheric ozone (O 3 ) [Wang and Shallcross, 2000], organic aerosols [Claeys et al., 2004], and climate change [Sanderson et al., 2003]. Local VOC emission data, representative of scales less than 1 km, are difficult to extrapolate, and consequently the magnitude and variabil- ity of these emissions is not well understood on conti- nental scales. Standard emission inventories based on ecosystem data and emission factors [Guenther et al., 2005] are poorly constrained. We have shown previously that observations of formaldehyde (HCHO) columns from the Global Ozone Monitoring Experiment (GOME) satel- lite instrument [Chance et al., 2000] provide information to estimate biogenic VOC emissions, specifically isoprene emissions, on a global scale and with resolution of the order of 100 km [Palmer et al., 2003]. We examine here the quantitative value of these data for better understand- D12315 1 of 14


Tellus B | 2007

Stomatal and non-stomatal fluxes of ozone to a northern mixed hardwood forest

Alan J. Hogg; Johan Uddling; David S. Ellsworth; Mary Anne Carroll; Shelley Pressley; Brian K. Lamb; Christoph S. Vogel

Measurements of ozone, sensible heat, and latent heat fluxes and plant physiological parameters were made at a northern mixed hardwood forest located at the University of Michigan Biological Station in northern Michigan from June 27 to September 28, 2002. These measurements were used to calculate total ozone flux and partitioning between stomatal and non-stomatal sinks. Total ozone flux varied diurnally with maximum values reaching 100 μmol m-2 h-1 at midday and minimums at or near zero at night. Mean daytime canopy conductance was 0.5 mol m-2 s-1. During daytime, non-stomatal ozone conductance accounted for as much as 66% of canopy conductance, with the non-stomatal sink representing 63% of the ozone flux. Stomatal conductance showed expected patterns of behaviour with respect to photosynthetic photon flux density (PPFD) and vapour pressure defecit (VPD). Non-stomatal conductance for ozone increased monotonically with increasing PPFD, increased with temperature (T) before falling off again at high T, and behaved similarly for VPD. Day-time non-stomatal ozone sinks are large and vary with time and environmental drivers, particularly PPFD and T. This information is crucial to deriving mechanistic models that can simulate ozone uptake by different vegetation types


Frontiers in Ecology and Evolution | 2017

Carbon and Water Budgets in Multiple Wheat-Based Cropping Systems in the Inland Pacific Northwest US: Comparison of CropSyst Simulations with Eddy Covariance Measurements

Jinshu Chi; Fidel Maureira; Sarah Waldo; Shelley Pressley; Claudio O. Stöckle; Patrick T. O'Keeffe; William L. Pan; Erin S. Brooks; Dave R. Huggins; Brian K. Lamb

Accurate carbon and water flux simulations for croplands are greatly dependent on high quality representation of management practices and meteorological conditions, which are key drivers of the surface-atmosphere exchange processes. Fourteen site-years of carbon and water fluxes were simulated using the CropSyst model over four agricultural sites in the inland Pacific Northwest US from October 1, 2011 to September 30, 2015. Model performance for field-scale net ecosystem exchange of CO2 (NEE) and evapotranspiration (ET) was evaluated by comparing simulations with long-term eddy covariance measurements. The model captured the temporal variations of NEE and ET reasonably well with an overall r of 0.78 and 0.80, and a low RMSE of 1.82 g C m-2 d-1 and 0.84 mm d-1 for NEE and ET, respectively. The model slightly underestimated NEE and ET by 0.51 g C m-2 d-1 and 0.09 mm d-1, respectively. ET simulations showed better agreement with eddy covariance measurements than NEE. The model performed much better for the sites with detailed initial conditions (e.g. SOC content) and management practice information (e.g. tillage type). The CropSyst results showed that the winter wheat fields could be annual net carbon sinks or close to neutral with the net ecosystem carbon balance (NECB) ranging from 92 to -17 g C m-2, while the spring crop fields were net carbon sources or neutral with an annual NECB of -327 to -3 g C m-2. Simulations for the paired tillage sites showed that the no-till site resulted in lower CO2 emissions for the crop rotations of winter wheat-spring garbanzo, but had higher carbon loss into the atmosphere for spring canola compared to the conventional tillage site. Water budgets did not differ significantly between the two tillage systems. Winter wheat in the high-rainfall area had higher crop yields and water use efficiency but emitted larger amounts of CO2 into the atmosphere than in the low-rainfall area. Based on model evaluations in this study, CropSyst appears promising as a tool to simulate field-scale carbon and water budgets and assess the effects of different management practices and local meteorological conditions for the wheat-based cropping systems in this region.


Journal of Sensor and Actuator Networks | 2017

Analyzing the Relationship between Human Behavior and Indoor Air Quality

Beiyu Lin; Yibo Huangfu; Nathan Lima; B. T. Jobson; Max Kirk; Patrick O’Keeffe; Shelley Pressley; Von P. Walden; Brian K. Lamb; Diane J. Cook

In the coming decades, as we experience global population growth and global aging issues, there will be corresponding concerns about the quality of the air we experience inside and outside buildings. Because we can anticipate that there will be behavioral changes that accompany population growth and aging, we examine the relationship between home occupant behavior and indoor air quality. To do this, we collect both sensor-based behavior data and chemical indoor air quality measurements in smart home environments. We introduce a novel machine learning-based approach to quantify the correlation between smart home features and chemical measurements of air quality, and evaluate the approach using two smart homes. The findings may help us understand the types of behavior that measurably impact indoor air quality. This information could help us plan for the future by developing an automated building system that would be used as part of a smart city.


Science and Technology for the Built Environment | 2018

Indoor air quality and wildfire smoke impacts in the Pacific Northwest

W. Max Kirk; Madeline Fuchs; Yibo Huangfu; Nathan Lima; Patrick T. O'Keeffe; Beiyu Lin; Tom Jobson; Shelley Pressley; Von P. Walden; Diane J. Cook; Brian K. Lamb

Efforts to improve energy efficiency in homes and buildings have led to tighter structures. However, these changes can also produce negative consequences for indoor air quality and human health. One of the dramatic effects of climate change and weather is the increase in destructive wildfires, such as those experienced in the Pacific Northwest during the summer of 2015. The current article presents data for measurements at two houses during periods with and without high levels of wildfire smoke outdoors. For each house, indoor and outdoor pollutant measurements were obtained for ozone (O3), fine particulate matter (PM2.5), and volatile organic compounds along with outdoor weather conditions and occupant activities including the use of windows and doors. The volatile organic compound measurements were obtained using a Proton Transfer Reaction Mass Spectrometer. Compounds monitored included acetonitrile (a biomass burning tracer), formaldehyde, acetaldehyde, methanol, acetone, benzene, toluene, and C2-alkylbenzenes (i.e., sum of xylenes and ethylbenzene), C3-alkylbenzenes (i.e., sum of trimethylbenzene, ethyltoluene, and propylbenzene isomers), and C4-alkylbenzenes (i.e., sum of tetramethylbenzene and its isomers). A carbon dioxide tracer method was used to measure in situ ventilation rates, and blower door tests were also completed to determine standard ventilation rates. For smoky periods with elevated outdoor pollutant levels, penetration factors, defined as the ratio of indoor/outdoor concentrations were quite low. Penetration factors for PM2.5 were 11% for H2 and 15% for H3, except when windows or doors were open. The penetration factors for O3 were also low at 24% for H2 and 5% for H3. Elevated indoor volatile organic compound levels were not typically associated with outdoor levels, but reflected significant indoor sources. During smoke events, acetonitrile, a biomass burning tracer compound, was elevated outdoors and indoors in both houses, and benzene was elevated outdoors and indoors in H3.


Journal of Geophysical Research | 2017

Effects of climatic conditions and management practices on agricultural carbon and water budgets in the inland Pacific Northwest USA

Jinshu Chi; Sarah Waldo; Shelley Pressley; Eric S. Russell; Patrick T. O'Keeffe; William L. Pan; David R. Huggins; Claudio O. Stöckle; Erin S. Brooks; Brian K. Lamb

Cropland is an important land cover influencing global carbon and water cycles. Variability of agricultural carbon and water fluxes depends on crop species, management practices, soil characteristics, and climatic conditions. In the context of climate change, it is critical to quantify the long-term effects of these environmental drivers and farming activities on carbon and water dynamics. Twenty site-years of carbon and water fluxes covering a large precipitation gradient and a variety of crop species and management practices were measured in the inland Pacific Northwest using the eddy covariance method. The rain-fed fields were net carbon sinks while the irrigated site was close to carbon neutral during the winter wheat crop years. Sites growing spring crops were either carbon sinks, sources, or neutral, varying with crops, rainfall zones, and tillage practices. Fluxes were more sensitive to variability in precipitation than temperature: annual carbon and water fluxes increased with the increasing precipitation while only respiration increased with temperature in the high-rainfall area. Compared to a nearby rain-fed site, irrigation improved winter wheat production but resulted in large losses of carbon and water to the atmosphere. Compared to conventional tillage, no-till had significantly lower respiration but resulted in slightly lower yields and water use efficiency over four years. Under future climate change, it is expected that more carbon fixation by crops and evapotranspiration would occur in a warmer and wetter environment.


Atmospheric Chemistry and Physics | 2007

Process-based estimates of terrestrial ecosystem isoprene emissions: incorporating the effects of a direct CO2-isoprene interaction

Almut Arneth; Ülo Niinemets; Shelley Pressley; Jaana Bäck; Pertti Hari; Thomas Karl; S. M. Noe; I. C. Prentice; D. Serça; Thomas Hickler; Annett Wolf; Benjamin Smith


Atmospheric Environment | 2005

Measurements of CO2 fluxes from the Mexico City urban landscape

Erik Velasco; Shelley Pressley; Eugene Allwine; Hal Westberg; Brian K. Lamb


Atmospheric Chemistry and Physics | 2009

Eddy covariance flux measurements of pollutant gases in urban Mexico City

Erik Velasco; Shelley Pressley; Rasa Grivicke; Eugene Allwine; T. Coons; W. Foster; B. T. Jobson; H. Westberg; R. Ramos; F. Hernández; Luisa T. Molina; Brian K. Lamb


Journal of Geophysical Research | 2005

Long‐term isoprene flux measurements above a northern hardwood forest

Shelley Pressley; Brian K. Lamb; Hal Westberg; Julia E. Flaherty; Jack Chen; Christoph S. Vogel

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Brian K. Lamb

Washington State University

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Hal Westberg

Washington State University

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Eugene Allwine

Washington State University

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B. T. Jobson

Washington State University

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Alex Guenther

Pacific Northwest National Laboratory

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Rasa Grivicke

Washington State University

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