Articles | Volume 3, issue 4
https://doi.org/10.5194/amt-3-959-2010
© Author(s) 2010. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/amt-3-959-2010
© Author(s) 2010. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
23 Jul 2010
A comparison of GC-FID and PTR-MS toluene measurements in ambient air under conditions of enhanced monoterpene loading
J. L. Ambrose
Department of Chemistry, University of New Hampshire, Durham, New Hampshire, USA
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
K. Haase
Department of Chemistry, University of New Hampshire, Durham, New Hampshire, USA
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
R. S. Russo
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
Y. Zhou
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
M. L. White
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
now at: Northern Essex Community College, Haverhill, Massachusetts, USA
E. K. Frinak
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
now at: USMA Network Science Center, West Point, New York, USA
C. Jordan
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
H. R. Mayne
Department of Chemistry, University of New Hampshire, Durham, New Hampshire, USA
R. Talbot
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
B. C. Sive
Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
Related subject area
Subject: Gases | Technique: In Situ Measurement | Topic: Validation and Intercomparisons
Real-time measurement of phase partitioning of organic compounds using a proton-transfer-reaction time-of-flight mass spectrometer coupled to a CHARON inlet
A quantitative comparison of methods used to measure smaller methane emissions typically observed from superannuated oil and gas infrastructure
Comparing airborne algorithms for greenhouse gas flux measurements over the Alberta oil sands
Intercomparison of commercial analyzers for atmospheric ethane and methane observations
Characterization of inexpensive metal oxide sensor performance for trace methane detection
Intercomparison of upper tropospheric and lower stratospheric water vapor measurements over the Asian Summer Monsoon during the StratoClim campaign
Air pollution measurement errors: is your data fit for purpose?
Performance characterization of low-cost air quality sensors for off-grid deployment in rural Malawi
Comment on “Comparison of ozone measurement methods in biomass burning smoke: an evaluation under field and laboratory conditions” by Long et al. (2021)
Homogenization of the Observatoire de Haute Provence electrochemical concentration cell (ECC) ozonesonde data record: comparison with lidar and satellite observations
Long-term behavior and stability of calibration models for NO and NO2 low-cost sensors
Controlled-release experiment to investigate uncertainties in UAV-based emission quantification for methane point sources
Ozone formation sensitivity study using machine learning coupled with the reactivity of volatile organic compound species
Evaluating uncertainty in sensor networks for urban air pollution insights
Estimating oil sands emissions using horizontal path-integrated column measurements
Global evaluation of the precipitable-water-vapor product from MERSI-II (Medium Resolution Spectral Imager) on board the Fengyun-3D satellite
Field testing two flux footprint models
Validation of a new cavity ring-down spectrometer for measuring tropospheric gaseous hydrogen chloride
Comparison of formaldehyde measurements by Hantzsch, CRDS and DOAS in the SAPHIR chamber
A field intercomparison of three passive air samplers for gaseous mercury in ambient air
Beef cattle methane emissions measured with tracer-ratio and inverse dispersion modelling techniques
Methane emissions from an oil sands tailings pond: a quantitative comparison of fluxes derived by different methods
Performance of open-path GasFinder3 devices for CH4 concentration measurements close to ambient levels
Water vapor density and turbulent fluxes from three generations of infrared gas analyzers
Quantifying fugitive gas emissions from an oil sands tailings pond with open-path Fourier transform infrared measurements
Robust statistical calibration and characterization of portable low-cost air quality monitoring sensors to quantify real-time O3 and NO2 concentrations in diverse environments
A miniature Portable Emissions Measurement System (PEMS) for real-driving monitoring of motorcycles
In situ measurement of CO2 and CH4 from aircraft over northeast China and comparison with OCO-2 data
Mobile-platform measurement of air pollutant concentrations in California: performance assessment, statistical methods for evaluating spatial variations, and spatial representativeness
Continuous methane concentration measurements at the Greenland ice sheet–atmosphere interface using a low-cost, low-power metal oxide sensor system
The development of the Atmospheric Measurements by Ultra-Light Spectrometer (AMULSE) greenhouse gas profiling system and application for satellite retrieval validation
Atmospheric observations of the water vapour continuum in the near-infrared windows between 2500 and 6600 cm−1
Intercomparison study of atmospheric 222Rn and 222Rn progeny monitors
Sources of error in open-path FTIR measurements of N2O and CO2 emitted from agricultural fields
Constraining the accuracy of flux estimates using OTM 33A
Evaluating the measurement interference of wet rotating-denuder–ion chromatography in measuring atmospheric HONO in a highly polluted area
Intercomparison of nitrous acid (HONO) measurement techniques in a megacity (Beijing)
Validity and limitations of simple reaction kinetics to calculate concentrations of organic compounds from ion counts in PTR-MS
Recent advances in measurement techniques for atmospheric carbon monoxide and nitrous oxide observations
True eddy accumulation trace gas flux measurements: proof of concept
Simultaneous detection of C2H6, CH4, and δ13C-CH4 using optical feedback cavity-enhanced absorption spectroscopy in the mid-infrared region: towards application for dissolved gas measurements
An improved low-power measurement of ambient NO2 and O3 combining electrochemical sensor clusters and machine learning
Comparison of slant open-path flux gradient and static closed chamber techniques to measure soil N2O emissions
Field measurements of methylglyoxal using proton transfer reaction time-of-flight mass spectrometry and comparison to the DNPH–HPLC–UV method
How well can global chemistry models calculate the reactivity of short-lived greenhouse gases in the remote troposphere, knowing the chemical composition
Estimation of nocturnal CO2 and N2O soil emissions from changes in surface boundary layer mass storage
Intra-urban spatial variability of surface ozone in Riverside, CA: viability and validation of low-cost sensors
Field calibration of electrochemical NO2 sensors in a citizen science context
Calibration and field testing of cavity ring-down laser spectrometers measuring CH4, CO2, and δ13CH4 deployed on towers in the Marcellus Shale region
Calibration and assessment of electrochemical air quality sensors by co-location with regulatory-grade instruments
Yarong Peng, Hongli Wang, Yaqin Gao, Shengao Jing, Shuhui Zhu, Dandan Huang, Peizhi Hao, Shengrong Lou, Tiantao Cheng, Cheng Huang, and Xuan Zhang
Atmos. Meas. Tech., 16, 15–28, https://doi.org/10.5194/amt-16-15-2023, https://doi.org/10.5194/amt-16-15-2023, 2023
Short summary
Short summary
This work examined the phase partitioning behaviors of organic compounds at hourly resolution in ambient conditions with the use of the CHemical Analysis of aeRosols ONline (CHARON) inlet coupled to a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS). Properly accounting for the neutral losses of small moieties during the molecular feature extraction from PTR mass spectra could significantly reduce uncertainties associated with the gas–particle partitioning measurements.
Stuart N. Riddick, Riley Ancona, Mercy Mbua, Clay S. Bell, Aidan Duggan, Timothy L. Vaughn, Kristine Bennett, and Daniel J. Zimmerle
Atmos. Meas. Tech., 15, 6285–6296, https://doi.org/10.5194/amt-15-6285-2022, https://doi.org/10.5194/amt-15-6285-2022, 2022
Short summary
Short summary
This describes controlled release experiments at the METEC facility in Fort Collins, USA, that investigates the accuracy and precision of five methods commonly used to measure methane emissions. Methods include static/dynamic chambers, hi flow sampling, a backward Lagrangian stochastic method, and a Gaussian plume method. This is the first time that methods for measuring CH4 emissions from point sources less than 200 g CH4 h−1 have been quantitively assessed against references and each other.
Broghan M. Erland, Cristen Adams, Andrea Darlington, Mackenzie L. Smith, Andrew K. Thorpe, Gregory R. Wentworth, Steve Conley, John Liggio, Shao-Meng Li, Charles E. Miller, and John A. Gamon
Atmos. Meas. Tech., 15, 5841–5859, https://doi.org/10.5194/amt-15-5841-2022, https://doi.org/10.5194/amt-15-5841-2022, 2022
Short summary
Short summary
Accurately estimating greenhouse gas (GHG) emissions is essential to reaching net-zero goals to combat the climate crisis. Airborne box-flights are ideal for assessing regional GHG emissions, as they can attain small error. We compare two box-flight algorithms and found they produce similar results, but daily variability must be considered when deriving emissions inventories. Increasing the consistency and agreement between airborne methods moves us closer to achieving more accurate estimates.
Roisin Commane, Andrew Hallward-Driemeier, and Lee T. Murray
Atmos. Meas. Tech. Discuss., https://doi.org/10.5194/amt-2022-272, https://doi.org/10.5194/amt-2022-272, 2022
Revised manuscript accepted for AMT
Short summary
Short summary
Methane / ethane ratios can be used to identify and partition the difference sources of methane, especially in areas with natural gas mixed with biogenic methane emissions, such as cities. We tested three commercially available laser-based analyzers for sensitivity, precision, size, power requirement, ease of use on mobile platforms, and expertise needed to operate the instrument and make recommendations for use in various situations.
Daniel Furuta, Tofigh Sayahi, Jinsheng Li, Bruce Wilson, Albert A. Presto, and Jiayu Li
Atmos. Meas. Tech., 15, 5117–5128, https://doi.org/10.5194/amt-15-5117-2022, https://doi.org/10.5194/amt-15-5117-2022, 2022
Short summary
Short summary
Methane is a major greenhouse gas and contributor to climate change with various human-caused and natural sources. Currently, atmospheric methane is expensive to sense. We investigate repurposing cheap methane safety sensors for atmospheric sensing, finding several promising sensors and identifying some of the challenges in this approach. This work will help in developing inexpensive sensor networks for methane monitoring, which will aid in reducing methane leaks and emissions.
Clare E. Singer, Benjamin W. Clouser, Sergey M. Khaykin, Martina Krämer, Francesco Cairo, Thomas Peter, Alexey Lykov, Christian Rolf, Nicole Spelten, Armin Afchine, Simone Brunamonti, and Elisabeth J. Moyer
Atmos. Meas. Tech., 15, 4767–4783, https://doi.org/10.5194/amt-15-4767-2022, https://doi.org/10.5194/amt-15-4767-2022, 2022
Short summary
Short summary
In situ measurements of water vapor in the upper troposphere are necessary to study cloud formation and hydration of the stratosphere but challenging due to cold–dry conditions. We compare measurements from three water vapor instruments from the StratoClim campaign in 2017. In clear sky (clouds), point-by-point differences were <1.5±8 % (<1±8 %). This excellent agreement allows detection of fine-scale structures required to understand the impact of convection on stratospheric water vapor.
Sebastian Diez, Stuart E. Lacy, Thomas J. Bannan, Michael Flynn, Tom Gardiner, David Harrison, Nicholas Marsden, Nicholas A. Martin, Katie Read, and Pete M. Edwards
Atmos. Meas. Tech., 15, 4091–4105, https://doi.org/10.5194/amt-15-4091-2022, https://doi.org/10.5194/amt-15-4091-2022, 2022
Short summary
Short summary
Regardless of the cost of the measuring instrument, there are no perfect measurements. For this reason, we compare the quality of the information provided by cheap devices when they are used to measure air pollutants and we try to emphasise that before judging the potential usefulness of the devices, the user must specify his own needs. Since commonly used performance indices/metrics can be misleading in qualifying this, we propose complementary visual analysis to the more commonly used metrics.
Ashley S. Bittner, Eben S. Cross, David H. Hagan, Carl Malings, Eric Lipsky, and Andrew P. Grieshop
Atmos. Meas. Tech., 15, 3353–3376, https://doi.org/10.5194/amt-15-3353-2022, https://doi.org/10.5194/amt-15-3353-2022, 2022
Short summary
Short summary
We present findings from a 1-year pilot deployment of low-cost integrated air quality sensor packages in rural Malawi using calibration models developed during collocation with US regulatory monitors. We compare the results with data from remote sensing products and previous field studies. We conclude that while the remote calibration approach can help extract useful data, great care is needed when assessing low-cost sensor data collected in regions without reference instrumentation.
Noah Bernays, Daniel A. Jaffe, Irina Petropavlovskikh, and Peter Effertz
Atmos. Meas. Tech., 15, 3189–3192, https://doi.org/10.5194/amt-15-3189-2022, https://doi.org/10.5194/amt-15-3189-2022, 2022
Short summary
Short summary
Ozone is an important pollutant that impacts millions of people worldwide. It is therefore important to ensure accurate measurements. A recent surge in wildfire activity in the USA has resulted in significant enhancements in ozone concentration. However given the nature of wildfire smoke, there are questions about our ability to accurately measure ozone. In this comment, we discuss possible biases in the UV measurements of ozone in the presence of smoke.
Gérard Ancellet, Sophie Godin-Beekmann, Herman G. J. Smit, Ryan M. Stauffer, Roeland Van Malderen, Renaud Bodichon, and Andrea Pazmiño
Atmos. Meas. Tech., 15, 3105–3120, https://doi.org/10.5194/amt-15-3105-2022, https://doi.org/10.5194/amt-15-3105-2022, 2022
Short summary
Short summary
The 1991–2021 Observatoire de Haute Provence electrochemical concentration cell (ECC) ozonesonde data have been homogenized according to the recommendations of the Ozonesonde Data Quality Assessment panel. Comparisons with ground-based instruments also measuring ozone at the same station (lidar, surface measurements) and with colocated satellite observations show the benefits of this homogenization. Remaining differences between ECC and other observations in the stratosphere are also discussed.
Horim Kim, Michael Müller, Stephan Henne, and Christoph Hüglin
Atmos. Meas. Tech., 15, 2979–2992, https://doi.org/10.5194/amt-15-2979-2022, https://doi.org/10.5194/amt-15-2979-2022, 2022
Short summary
Short summary
In this study, the performance of electrochemical sensors for NO and NO2 for measuring air quality was determined over a longer operating period. The performance of NO sensors remained reliable for more than 18 months. However, the NO2 sensors showed decreasing performance over time. During deployment, we found that the NO2 sensors can distinguish general pollution levels, but they proved unsuitable for accurate measurements due to significant biases.
Randulph Morales, Jonas Ravelid, Katarina Vinkovic, Piotr Korbeń, Béla Tuzson, Lukas Emmenegger, Huilin Chen, Martina Schmidt, Sebastian Humbel, and Dominik Brunner
Atmos. Meas. Tech., 15, 2177–2198, https://doi.org/10.5194/amt-15-2177-2022, https://doi.org/10.5194/amt-15-2177-2022, 2022
Short summary
Short summary
Mapping trace gas emission plumes using in situ measurements from unmanned aerial vehicles (UAVs) is an emerging and attractive possibility to quantify emissions from localized sources. We performed an extensive controlled-release experiment to develop an optimal quantification method and to determine the related uncertainties under various environmental and sampling conditions. Our approach was successful in quantifying local methane sources from drone-based measurements.
Junlei Zhan, Yongchun Liu, Wei Ma, Xin Zhang, Xuezhong Wang, Fang Bi, Yujie Zhang, Zhenhai Wu, and Hong Li
Atmos. Meas. Tech., 15, 1511–1520, https://doi.org/10.5194/amt-15-1511-2022, https://doi.org/10.5194/amt-15-1511-2022, 2022
Short summary
Short summary
Our study investigated the O3 formation sensitivity in Beijing using a random forest model coupled with the reactivity of volatile organic
compound (VOC) species. Results found that random forest accurately predicted O3 concentration when initial VOCs were considered, and relative importance correlated well with O3 formation potential. The O3 isopleth curves calculated by the random forest model were generally comparable with those calculated by the box model.
Daniel R. Peters, Olalekan A. M. Popoola, Roderic L. Jones, Nicholas A. Martin, Jim Mills, Elizabeth R. Fonseca, Amy Stidworthy, Ella Forsyth, David Carruthers, Megan Dupuy-Todd, Felicia Douglas, Katie Moore, Rishabh U. Shah, Lauren E. Padilla, and Ramón A. Alvarez
Atmos. Meas. Tech., 15, 321–334, https://doi.org/10.5194/amt-15-321-2022, https://doi.org/10.5194/amt-15-321-2022, 2022
Short summary
Short summary
We present more than 2 years of NO2 pollution measurements from a sensor network in Greater London and compare results to an extensive network of expensive reference-grade monitors. We show the ability of our lower-cost network to generate robust insights about local air pollution. We also show how irregularities in sensor performance lead to some uncertainty in results and demonstrate ways that future users can characterize and mitigate uncertainties to get the most value from sensor data.
Timothy G. Pernini, T. Scott Zaccheo, Jeremy Dobler, and Nathan Blume
Atmos. Meas. Tech., 15, 225–240, https://doi.org/10.5194/amt-15-225-2022, https://doi.org/10.5194/amt-15-225-2022, 2022
Short summary
Short summary
We demonstrate a novel approach to estimating emissions from oil sands operations that utilizes the GreenLITE™ gas concentration measurement system and an atmospheric model. While deployed at a facility in the Athabasca region of Alberta, Canada, CH4 emissions from a tailings pond were estimated to be 7.2 t/d for July–October 2019, and 5.1 t/d for March–July 2020. CH4 emissions from an open-pit mine were estimated to be 24.6 t/d for September–October 2019.
Wengang Zhang, Ling Wang, Yang Yu, Guirong Xu, Xiuqing Hu, Zhikang Fu, and Chunguang Cui
Atmos. Meas. Tech., 14, 7821–7834, https://doi.org/10.5194/amt-14-7821-2021, https://doi.org/10.5194/amt-14-7821-2021, 2021
Short summary
Short summary
Global precipitable water vapor (PWV) derived from MERSI-II (Medium Resolution Spectral Imager) is compared with PWV from the Integrated Global Radiosonde Archive (IGRA). Our results show a good agreement between PWV from MERSI-II and IGRA and that MERSI-II PWV is slightly underestimated on the whole, especially in summer. The bias between MERSI-II and IGRA grows with a larger spatial distance between the footprint of the satellite and the IGRA station, as well as increasing PWV.
Trevor W. Coates, Monzurul Alam, Thomas K. Flesch, and Guillermo Hernandez-Ramirez
Atmos. Meas. Tech., 14, 7147–7152, https://doi.org/10.5194/amt-14-7147-2021, https://doi.org/10.5194/amt-14-7147-2021, 2021
Short summary
Short summary
A field study tested two footprint models for calculating surface emissions from downwind flux measurements. Emission rates from a 10 × 10 m synthetic source were estimated with the simple Kormann–Meixner model and a sophisticated Lagrangian stochastic model. Both models underestimated emissions by approximately 30 %, and no statistical differences were observed between the models. Footprint models are critically important for interpreting eddy covariance measurements.
Teles C. Furlani, Patrick R. Veres, Kathryn E. R. Dawe, J. Andrew Neuman, Steven S. Brown, Trevor C. VandenBoer, and Cora J. Young
Atmos. Meas. Tech., 14, 5859–5871, https://doi.org/10.5194/amt-14-5859-2021, https://doi.org/10.5194/amt-14-5859-2021, 2021
Short summary
Short summary
This study characterized and validated a commercial spectroscopic instrument for the measurement of hydrogen chloride (HCl) in the atmosphere. Near the Earth’s surface, HCl acts as the dominant reservoir for other chlorine-containing reactive chemicals that play an important role in atmospheric chemistry. The properties of HCl make it challenging to measure. This instrument can overcome many of these challenges, enabling reliable HCl measurements.
Marvin Glowania, Franz Rohrer, Hans-Peter Dorn, Andreas Hofzumahaus, Frank Holland, Astrid Kiendler-Scharr, Andreas Wahner, and Hendrik Fuchs
Atmos. Meas. Tech., 14, 4239–4253, https://doi.org/10.5194/amt-14-4239-2021, https://doi.org/10.5194/amt-14-4239-2021, 2021
Short summary
Short summary
Three instruments that use different techniques to measure gaseous formaldehyde concentrations were compared in experiments in the atmospheric simulation chamber SAPHIR at Forschungszentrum Jülich. The results demonstrated the need to correct the baseline in measurements by instruments that use the Hantzsch reaction or make use of cavity ring-down spectroscopy. After applying corrections, all three methods gave accurate and precise measurements within their specifications.
Attilio Naccarato, Antonella Tassone, Maria Martino, Sacha Moretti, Antonella Macagnano, Emiliano Zampetti, Paolo Papa, Joshua Avossa, Nicola Pirrone, Michelle Nerentorp, John Munthe, Ingvar Wängberg, Geoff W. Stupple, Carl P. J. Mitchell, Adam R. Martin, Alexandra Steffen, Diana Babi, Eric M. Prestbo, Francesca Sprovieri, and Frank Wania
Atmos. Meas. Tech., 14, 3657–3672, https://doi.org/10.5194/amt-14-3657-2021, https://doi.org/10.5194/amt-14-3657-2021, 2021
Short summary
Short summary
Mercury monitoring in support of the Minamata Convention requires effective and reliable analytical tools. Passive sampling is a promising approach for creating a sustainable long-term network for atmospheric mercury with improved spatial resolution and global coverage. In this study the analytical performance of three passive air samplers (CNR-PAS, IVL-PAS, and MerPAS) was assessed over extended deployment periods and the accuracy of concentrations was judged by comparison with active sampling.
Mei Bai, José I. Velazco, Trevor W. Coates, Frances A. Phillips, Thomas K. Flesch, Julian Hill, David G. Mayer, Nigel W. Tomkins, Roger S. Hegarty, and Deli Chen
Atmos. Meas. Tech., 14, 3469–3479, https://doi.org/10.5194/amt-14-3469-2021, https://doi.org/10.5194/amt-14-3469-2021, 2021
Short summary
Short summary
The development and validation of management practices to mitigate methane (CH4) emissions from livestock require accurate emission measurements. We compared the inverse dispersion modelling (IDM) and tracer-ratio techniques to measure CH4 emissions from cattle. Both measurements agreed well but were higher than IPCC estimates. We suggest that the IDM approach can provide an accurate method of estimating cattle emissions, and IPCC estimates may have larger uncertainties.
Yuan You, Ralf M. Staebler, Samar G. Moussa, James Beck, and Richard L. Mittermeier
Atmos. Meas. Tech., 14, 1879–1892, https://doi.org/10.5194/amt-14-1879-2021, https://doi.org/10.5194/amt-14-1879-2021, 2021
Short summary
Short summary
Tailings ponds in the Alberta oil sands can be significant sources of methane, an important greenhouse gas. This paper describes a 1-month study conducted in 2017 to measure methane emissions from a pond using a variety of micrometeorological flux methods and demonstrates some advantages of these methods over flux chambers.
Christoph Häni, Marcel Bühler, Albrecht Neftel, Christof Ammann, and Thomas Kupper
Atmos. Meas. Tech., 14, 1733–1741, https://doi.org/10.5194/amt-14-1733-2021, https://doi.org/10.5194/amt-14-1733-2021, 2021
Seth Kutikoff, Xiaomao Lin, Steven R. Evett, Prasanna Gowda, David Brauer, Jerry Moorhead, Gary Marek, Paul Colaizzi, Robert Aiken, Liukang Xu, and Clenton Owensby
Atmos. Meas. Tech., 14, 1253–1266, https://doi.org/10.5194/amt-14-1253-2021, https://doi.org/10.5194/amt-14-1253-2021, 2021
Short summary
Short summary
Fast-response infrared gas sensors have been used over 3 decades for long-term monitoring of water vapor fluxes. As optically improved infrared gas sensors are newly employed, we evaluated the performance of water vapor density and water vapor flux from three generations of infrared gas sensors in Bushland, Texas, USA. From our experiments, fluxes from the old sensors were best representative of evapotranspiration based on a world-class lysimeter reference measurement.
Yuan You, Samar G. Moussa, Lucas Zhang, Long Fu, James Beck, and Ralf M. Staebler
Atmos. Meas. Tech., 14, 945–959, https://doi.org/10.5194/amt-14-945-2021, https://doi.org/10.5194/amt-14-945-2021, 2021
Short summary
Short summary
Tailings ponds in the Alberta oil sands represent an insufficiently characterized source of fugitive emissions of pollutants to the atmosphere. In this study, a novel approach of using a Fourier transform infrared spectrometer along with measurements of atmospheric turbulence is shown to present a practical, non-intrusive method of quantifying emission rates for ammonia, alkanes, and methane. Results from a 1-month field study are presented and discussed.
Ravi Sahu, Ayush Nagal, Kuldeep Kumar Dixit, Harshavardhan Unnibhavi, Srikanth Mantravadi, Srijith Nair, Yogesh Simmhan, Brijesh Mishra, Rajesh Zele, Ronak Sutaria, Vidyanand Motiram Motghare, Purushottam Kar, and Sachchida Nand Tripathi
Atmos. Meas. Tech., 14, 37–52, https://doi.org/10.5194/amt-14-37-2021, https://doi.org/10.5194/amt-14-37-2021, 2021
Short summary
Short summary
A unique feature of our low-cost sensor deployment is a swap-out experiment wherein four of the six sensors were relocated to different sites in the two phases. The swap-out experiment is crucial in investigating the efficacy of calibration models when applied to weather and air quality conditions vastly different from those present during calibration. We developed a novel local calibration algorithm based on metric learning that offers stable and accurate calibration performance.
Michal Vojtisek-Lom, Alessandro A. Zardini, Martin Pechout, Lubos Dittrich, Fausto Forni, François Montigny, Massimo Carriero, Barouch Giechaskiel, and Giorgio Martini
Atmos. Meas. Tech., 13, 5827–5843, https://doi.org/10.5194/amt-13-5827-2020, https://doi.org/10.5194/amt-13-5827-2020, 2020
Short summary
Short summary
The feasibility of monitoring on-road emissions from small motorcycles with two highly compact portable emissions monitoring systems was evaluated on three motorcycles, with positive results. Mass emissions measured on the road were consistent among repeated runs, with differences between laboratory and on-road tests much larger than those between portable and laboratory systems, which were, on the average, within units of percent over standard test cycles.
Xiaoyu Sun, Minzheng Duan, Yang Gao, Rui Han, Denghui Ji, Wenxing Zhang, Nong Chen, Xiangao Xia, Hailei Liu, and Yanfeng Huo
Atmos. Meas. Tech., 13, 3595–3607, https://doi.org/10.5194/amt-13-3595-2020, https://doi.org/10.5194/amt-13-3595-2020, 2020
Short summary
Short summary
The accurate measurement of greenhouse gases and their vertical distribution in the atmosphere is significant to the study of climate change and satellite remote sensing. Carbon dioxide and methane between 0.6 and 7 km were measured by the aircraft King Air 350ER in Jiansanjiang, northeast China, on 7–11 August 2018. The profiles show strong variation with the altitude and time, so the vertical structure of gases should be taken into account in the current satellite retrieval algorithm.
Paul A. Solomon, Dena Vallano, Melissa Lunden, Brian LaFranchi, Charles L. Blanchard, and Stephanie L. Shaw
Atmos. Meas. Tech., 13, 3277–3301, https://doi.org/10.5194/amt-13-3277-2020, https://doi.org/10.5194/amt-13-3277-2020, 2020
Short summary
Short summary
Analyzing street-level air pollutants (2016–2017), this assessment indicates that mobile measurement is precise and accurate (5 % to 25 % bias) relative to regulatory sites, with higher spatial resolution. Collocated sensor measurements in California showed differences less than 20 %, suggesting that greater differences represent spatial variability. Mobile data confirm regulatory-site spatial representation and that pollutant levels can also be 6 to 8 times higher just blocks apart.
Christian Juncher Jørgensen, Jacob Mønster, Karsten Fuglsang, and Jesper Riis Christiansen
Atmos. Meas. Tech., 13, 3319–3328, https://doi.org/10.5194/amt-13-3319-2020, https://doi.org/10.5194/amt-13-3319-2020, 2020
Short summary
Short summary
Recent discoveries have shown large emissions of methane (CH4) to the atmosphere from meltwater at the Greenland ice sheet (GrIS). Low-cost and low-power gas sensor technology offers great potential to supplement CH4 measurements using very expensive reference analyzers under harsh and remote conditions. In this paper we evaluate the in situ performance at the GrIS of a low-cost CH4 sensor to a state-of-the-art analyzer and find very excellent agreement between the two methods.
Lilian Joly, Olivier Coopmann, Vincent Guidard, Thomas Decarpenterie, Nicolas Dumelié, Julien Cousin, Jérémie Burgalat, Nicolas Chauvin, Grégory Albora, Rabih Maamary, Zineb Miftah El Khair, Diane Tzanos, Joël Barrié, Éric Moulin, Patrick Aressy, and Anne Belleudy
Atmos. Meas. Tech., 13, 3099–3118, https://doi.org/10.5194/amt-13-3099-2020, https://doi.org/10.5194/amt-13-3099-2020, 2020
Short summary
Short summary
This article presents an instrument weighing less than 3 kg for accurate and rapid measurement of greenhouse gases between 0 and 30 km altitude using a meteorological balloon. This article shows the interest of these measurements for the validation of simulations of infrared satellite observations.
Jonathan Elsey, Marc D. Coleman, Tom D. Gardiner, Kaah P. Menang, and Keith P. Shine
Atmos. Meas. Tech., 13, 2335–2361, https://doi.org/10.5194/amt-13-2335-2020, https://doi.org/10.5194/amt-13-2335-2020, 2020
Short summary
Short summary
Water vapour is an important component in trying to understand the flows of energy between the Sun and Earth, since it is opaque to radiation emitted by both the surface and the Sun. In this paper, we study how it absorbs sunlight by way of its
continuum, a property which is poorly understood and with few measurements. Our results indicate that this continuum absorption may be more significant than previously thought, potentially impacting satellite observations and climate studies.
Claudia Grossi, Scott D. Chambers, Olivier Llido, Felix R. Vogel, Victor Kazan, Alessandro Capuana, Sylvester Werczynski, Roger Curcoll, Marc Delmotte, Arturo Vargas, Josep-Anton Morguí, Ingeborg Levin, and Michel Ramonet
Atmos. Meas. Tech., 13, 2241–2255, https://doi.org/10.5194/amt-13-2241-2020, https://doi.org/10.5194/amt-13-2241-2020, 2020
Short summary
Short summary
The sustainable support of radon metrology at the environmental level offers new scientific possibilities for the quantification of greenhouse gas (GHG) emissions and the determination of their source terms as well as for the identification of radioactive sources for the assessment of radiation exposure. This study helps to harmonize the techniques commonly used for atmospheric radon and radon progeny activity concentration measurements.
Cheng-Hsien Lin, Richard H. Grant, Albert J. Heber, and Cliff T. Johnston
Atmos. Meas. Tech., 13, 2001–2013, https://doi.org/10.5194/amt-13-2001-2020, https://doi.org/10.5194/amt-13-2001-2020, 2020
Short summary
Short summary
Gas quantification using the open-path Fourier transform infrared spectrometer (OP-FTIR) is subject to interferences of environmental variables, leading to errors in gas concentration calculations. This study investigated the effects of ambient water vapour content, temperature, path lengths, and wind speed on the quantification of N2O and CO2 concentrations, which can help the OP-FTIR users to avoid these errors and improve the precision and accuracy of the atmospheric gas quantification.
Rachel Edie, Anna M. Robertson, Robert A. Field, Jeffrey Soltis, Dustin A. Snare, Daniel Zimmerle, Clay S. Bell, Timothy L. Vaughn, and Shane M. Murphy
Atmos. Meas. Tech., 13, 341–353, https://doi.org/10.5194/amt-13-341-2020, https://doi.org/10.5194/amt-13-341-2020, 2020
Short summary
Short summary
Ground-based measurements of emissions from oil and natural gas production are important for understanding emission distributions and improving emission inventories. Here, measurement technique Other Test Method 33A (OTM 33A) is validated through several test releases staged at the Methane Emissions Technology Evaluation Center. These tests suggest OTM 33A has no inherent bias and that a group of OTM measurements is within 5 % of the known mean emission rate.
Zheng Xu, Yuliang Liu, Wei Nie, Peng Sun, Xuguang Chi, and Aijun Ding
Atmos. Meas. Tech., 12, 6737–6748, https://doi.org/10.5194/amt-12-6737-2019, https://doi.org/10.5194/amt-12-6737-2019, 2019
Short summary
Short summary
We evaluated the performance of HONO measurement by a wet-denuder--ion0chromatography system (WD/IC, MARGA). We found significant artificial HONO formed from the reaction of NO2 oxidizing SO2 in the denuder solution. High ambient NH3 would elevate the pH of the denuder solution and promote the overestimation of HONO. A method was established to correct the HONO measurement by WD/IC instruments.
Leigh R. Crilley, Louisa J. Kramer, Bin Ouyang, Jun Duan, Wenqian Zhang, Shengrui Tong, Maofa Ge, Ke Tang, Min Qin, Pinhua Xie, Marvin D. Shaw, Alastair C. Lewis, Archit Mehra, Thomas J. Bannan, Stephen D. Worrall, Michael Priestley, Asan Bacak, Hugh Coe, James Allan, Carl J. Percival, Olalekan A. M. Popoola, Roderic L. Jones, and William J. Bloss
Atmos. Meas. Tech., 12, 6449–6463, https://doi.org/10.5194/amt-12-6449-2019, https://doi.org/10.5194/amt-12-6449-2019, 2019
Short summary
Short summary
Nitrous acid (HONO) is key species for understanding tropospheric chemistry, yet accurate and precise measurements are challenging. Here we report an inter–comparison exercise of a number of instruments that measured HONO in a highly polluted location (Beijing). All instruments agreed on the temporal trends yet displayed divergence in absolute concentrations. The cause of this divergence was unclear, but it may in part be due to spatial variability in instrument location.
Rupert Holzinger, W. Joe F. Acton, William J. Bloss, Martin Breitenlechner, Leigh R. Crilley, Sébastien Dusanter, Marc Gonin, Valerie Gros, Frank N. Keutsch, Astrid Kiendler-Scharr, Louisa J. Kramer, Jordan E. Krechmer, Baptiste Languille, Nadine Locoge, Felipe Lopez-Hilfiker, Dušan Materić, Sergi Moreno, Eiko Nemitz, Lauriane L. J. Quéléver, Roland Sarda Esteve, Stéphane Sauvage, Simon Schallhart, Roberto Sommariva, Ralf Tillmann, Sergej Wedel, David R. Worton, Kangming Xu, and Alexander Zaytsev
Atmos. Meas. Tech., 12, 6193–6208, https://doi.org/10.5194/amt-12-6193-2019, https://doi.org/10.5194/amt-12-6193-2019, 2019
Christoph Zellweger, Rainer Steinbrecher, Olivier Laurent, Haeyoung Lee, Sumin Kim, Lukas Emmenegger, Martin Steinbacher, and Brigitte Buchmann
Atmos. Meas. Tech., 12, 5863–5878, https://doi.org/10.5194/amt-12-5863-2019, https://doi.org/10.5194/amt-12-5863-2019, 2019
Short summary
Short summary
We analysed results obtained through CO and N2O performance audits conducted within the framework of the Global Atmosphere Watch (GAW) quality management system of the World Meteorology Organization (WMO). The results reveal that current spectroscopic measurement techniques have clear advantages with respect to data quality objectives compared to more traditional methods. Further, they allow for a smooth continuation of historic CO and N2O time series.
Lukas Siebicke and Anas Emad
Atmos. Meas. Tech., 12, 4393–4420, https://doi.org/10.5194/amt-12-4393-2019, https://doi.org/10.5194/amt-12-4393-2019, 2019
Short summary
Short summary
We present the emerging flux measurement method
true eddy accumulation(TEA), able to quantify the land–atmosphere exchange of a large number of trace gases which are important for air quality and atmospheric composition. Our innovative implementation provides proof of concept of TEA and compared well to the established reference, outperforming previous works on TEA. Key to the success was the innovative high-speed air sampling and fully digital real-time data processing system.
Loic Lechevallier, Roberto Grilli, Erik Kerstel, Daniele Romanini, and Jérôme Chappellaz
Atmos. Meas. Tech., 12, 3101–3109, https://doi.org/10.5194/amt-12-3101-2019, https://doi.org/10.5194/amt-12-3101-2019, 2019
Short summary
Short summary
In this work we describe a highly sensitive optical spectrometer for simultaneous measurement of methane, ethane, and the isotopic composition of methane. The coupling of the spectrometer with a dissolved gas extraction system will provide a suitable tool for understanding the origins of the dissolved hydrocarbons and discriminate between the different sources (e.g., biogenic vs. thermogenic).
Kate R. Smith, Peter M. Edwards, Peter D. Ivatt, James D. Lee, Freya Squires, Chengliang Dai, Richard E. Peltier, Mat J. Evans, Yele Sun, and Alastair C. Lewis
Atmos. Meas. Tech., 12, 1325–1336, https://doi.org/10.5194/amt-12-1325-2019, https://doi.org/10.5194/amt-12-1325-2019, 2019
Short summary
Short summary
Clusters of low-cost, low-power atmospheric gas sensors were built into a sensor instrument to monitor NO2 and O3 in Beijing, alongside reference instruments, aiming to improve the reliability of sensor measurements. Clustering identical sensors and using the median sensor signal was used to minimize drift over short and medium timescales. Three different machine learning techniques were used for all the sensor data in an attempt to correct for cross-interferences, which worked to some degree.
Mei Bai, Helen Suter, Shu Kee Lam, Thomas K. Flesch, and Deli Chen
Atmos. Meas. Tech., 12, 1095–1102, https://doi.org/10.5194/amt-12-1095-2019, https://doi.org/10.5194/amt-12-1095-2019, 2019
Short summary
Short summary
Improving direct field measurement techniques to quantify gas emissions from large agriculture farm is challenging. We measured nitrous oxide (N2O) emissions with static closed chambers and slant open-path flux gradient (FG) approaches following chicken manure application. The concurrent emission ratios (FG / chamber) showed N2O fluxes measured by FG were 1.22-1.40 times higher than those from the chambers. This study provides important information for the agriculture gas measurement community.
Vincent Michoud, Stéphane Sauvage, Thierry Léonardis, Isabelle Fronval, Alexandre Kukui, Nadine Locoge, and Sébastien Dusanter
Atmos. Meas. Tech., 11, 5729–5740, https://doi.org/10.5194/amt-11-5729-2018, https://doi.org/10.5194/amt-11-5729-2018, 2018
Short summary
Short summary
This study presents the first measurements of ambient methylglyoxal, an important atmospheric α-dicarbonyl, using proton transfer reaction time-of-flight mass spectrometry. These measurements mostly agree with concomitant measurements from a reference technique: the DNPH derivatization technique and high-performance liquid chromatography with UV detection. In addition, a careful investigation of the differences between the two techniques is carried out to explain the disagreements observed.
Michael J. Prather, Clare M. Flynn, Xin Zhu, Stephen D. Steenrod, Sarah A. Strode, Arlene M. Fiore, Gustavo Correa, Lee T. Murray, and Jean-Francois Lamarque
Atmos. Meas. Tech., 11, 2653–2668, https://doi.org/10.5194/amt-11-2653-2018, https://doi.org/10.5194/amt-11-2653-2018, 2018
Short summary
Short summary
A new protocol for merging in situ atmospheric chemistry measurements with 3-D models is developed. This technique can identify the most reactive air parcels in terms of tropospheric production/loss of O3 & CH4. This approach highlights differences in 6 global chemistry models even with composition specified. Thus in situ measurements from, e.g., NASA's ATom mission can be used to develop a chemical climatology of, not only the key species, but also the rates of key reactions in each air parcel.
Richard H. Grant and Rex A. Omonode
Atmos. Meas. Tech., 11, 2119–2133, https://doi.org/10.5194/amt-11-2119-2018, https://doi.org/10.5194/amt-11-2119-2018, 2018
Short summary
Short summary
Annual emissions of trace gases requires knowledge of the emissions throughout the day and year. Unfortunately emissions into the surface boundary layer during calm nights are rarely measured. During such conditions surface layer concentrations of carbon dioxide (CO2) and nitrous oxide (N2O) often accumulate in the surface boundary layer and the time rate of change of this accumulation was used to estimate emissions. Results showed this approach to be reasonable.
Kira Sadighi, Evan Coffey, Andrea Polidori, Brandon Feenstra, Qin Lv, Daven K. Henze, and Michael Hannigan
Atmos. Meas. Tech., 11, 1777–1792, https://doi.org/10.5194/amt-11-1777-2018, https://doi.org/10.5194/amt-11-1777-2018, 2018
Short summary
Short summary
Ground-level ozone has negative human health impacts. In the summer of 2015, 13 low-cost sensor monitors were deployed to several neighborhoods around Riverside, California. There were significant spatial differences between monitors. This is important because it means that ozone in certain places may be higher than what EPA monitors report for an area, which is pertinent for residents of those communities. This research helps inform the limitations and advantages of low-cost sensor networks.
Bas Mijling, Qijun Jiang, Dave de Jonge, and Stefano Bocconi
Atmos. Meas. Tech., 11, 1297–1312, https://doi.org/10.5194/amt-11-1297-2018, https://doi.org/10.5194/amt-11-1297-2018, 2018
Short summary
Short summary
Although in many cities the population is exposed to air pollution, real-time air quality is usually only measured at a few locations. New low-cost sensor technology has the potential to extend the monitoring network significantly. We show that citizen science campaigns using the current generations of electrochemical NO2 sensors may provide useful complementary data on local air quality in an urban setting, provided that experiments are properly set up and the data are carefully analysed.
Natasha L. Miles, Douglas K. Martins, Scott J. Richardson, Christopher W. Rella, Caleb Arata, Thomas Lauvaux, Kenneth J. Davis, Zachary R. Barkley, Kathryn McKain, and Colm Sweeney
Atmos. Meas. Tech., 11, 1273–1295, https://doi.org/10.5194/amt-11-1273-2018, https://doi.org/10.5194/amt-11-1273-2018, 2018
Short summary
Short summary
Analyzers measuring methane and methane isotopic ratio were deployed at four towers in the Marcellus Shale natural gas extraction region of Pennsylvania. The methane isotopic ratio is helpful for differentiating emissions from natural gas activities from other sources (e.g., landfills). We describe the analyzer calibration. The signals observed in the study region were generally small, but the instrumental performance demonstrated here could be used in regions with stronger enhancements.
David H. Hagan, Gabriel Isaacman-VanWertz, Jonathan P. Franklin, Lisa M. M. Wallace, Benjamin D. Kocar, Colette L. Heald, and Jesse H. Kroll
Atmos. Meas. Tech., 11, 315–328, https://doi.org/10.5194/amt-11-315-2018, https://doi.org/10.5194/amt-11-315-2018, 2018
Short summary
Short summary
The use of low-cost sensors for air pollution research has outpaced our understanding of their capabilities and limitations under real-world conditions. Here we describe the deployment, calibration and evaluation of electrochemical sensors on the Island of Hawai‘i. We obtain excellent performance (RMSE < 7 ppb, r2 = 0.997) across a wide dynamic range (1 ppb–2 ppm). We introduce a hybrid regression algorithm which works across a large dynamic range and shows little decay in sensitivity over time.
Cited articles
Ambrose, J. L., Mao, H., Mayne, H. R., Stutz, J., Talbot, R., and Sive, B. C.: Nighttime nitrate radical chemistry at Appledore Island, Maine during the 2004 International Consortium for Atmospheric Research on Transport and Transformation, J. Geophys. Res., 112, D21302, https://doi.org/10.1029/2007JD008756, 2007.
Andreae, M. O. and Merlet, P.: Emission of trace gases and aerosols from biomass burning, Global Biogeochem. Cy., 15, 955–966, 2001.
Apel, E. C., Calvert, J. G., Greenberg, J. P., Riemer, D., Zika, R., Kleindienst, T. E., Lonneman, W. A., Fung, K., and Fujita, E.: Generation and validation of oxygenated volatile organic carbon standards for the 1995 Southern Oxidants Study Nashville Intensive, J. Geophys. Res., 103, 22281–22944, 1998.
Apel, E. C., Hills, A. J., Leub, R., Zindel, S., Eisele, S., and Riemer, D. D.: A fast-GC/MS system to measure C2 to C4 carbonyls and methanol aboard aircraft, J. Geophys. Res., 108, D20, 8794, https://doi.org/10.1029/2002JD003199, 2003.
Atkinson, R.: Kinetics and mechanisms of the gas-phase reactions of the hydroxyl radical with organic compounds, J. Phys. Chem. Ref. Data, 1, 1–246, 1989.
Atkinson, R.: Gas-phase tropospheric chemistry of organic compounds, J. Phys. Chem. Ref. Data Monogr., 2, 1–216, 1994.
Atkinson, R.: Gas-phase tropospheric chemistry of volatile organic compounds: 1. Alkanes and alkenes, J. Phys. Chem. Ref. Data, 26, 215–290, 1997.
Atkinson, R. and Arey, J.: Gas-phase tropospheric chemistry of biogenic volatile organic compounds: a review, Atmos. Environ, 37, S2, S197–S219, 2003.
Atkinson, R., Baulch, D. L., Cox, R. A., Crowley, J. N., Hampson, R. F., Hynes, R. G., Jenkin, M. E., Rossi, M. J., and Troe, J.: Evaluated kinetic and photochemical data for atmospheric chemistry: Volume I – gas phase reactions of Ox, HOx, NOx and SOx species, Atmos. Chem. Phys., 4, 1461–1738, https://doi.org/10.5194/acp-4-1461-2004, 2004.
Atkinson, R., Baulch, D. L., Cox, R. A., Crowley, J. N., Hampson, R. F., Hynes, R. G., Jenkin, M. E., Rossi, M. J., Troe, J., and IUPAC Subcommittee: Evaluated kinetic and photochemical data for atmospheric chemistry: Volume II – gas phase reactions of organic species, Atmos. Chem. Phys., 6, 3625–4055, https://doi.org/10.5194/acp-6-3625-2006, 2006.
Blake, R. S., Monks, P. S., and Ellis, A. M.: Proton-Transfer Reaction Mass Spectrometry, Chem. Rev., 109, 861–896, 2009.
Christian, T. J., Kleiss, B., Yokelson, R. J., Holzinger, R., Crutzen, P. J., Hao, W. M., Shirai, T., and Blake, D. R.: Comprehensive laboratory measurements of biomass-burning emissions: 2. First intercomparison of open-path FTIR, PTR-MS, and GC-MS/FID/ECD, J. Geophys. Res., 109, D02311, https://doi.org/10.1029/2003JD003874, 2004.
Dalton, I., Albritton, D. L., Lindinger, W., and Pahl, M.: Mobilities of CO2+, N2H+, H3O+, H3O+H2O, and H3O+(H2O)2 ions in N2, J. Chem. Phys., 65, 5028–5030, 1976.
de Bievre, P. and Taylor, P. D. P.: Table of isotopic compositions of the elements, Int. J. Mass Spectrom., 123, 149–166, 1993.
de Gouw, J. A., Goldan, P. D., Warneke, C., Kuster, W. C., Roberts, J. M., Marchewka, M., Bertman, S. B., Pszenny, A. A. P., and Keene, W. C.: Validation of proton transfer reaction-mass spectrometry (PTR-MS) measurements of gas-phase organic compounds in the atmosphere during the New England Air Quality Study (NEAQS) in 2002, J. Geophys. Res., 108, D21, 4682, https://doi.org/10.1029/2003JD003863, 2003a.
de Gouw, J. and Warneke, C.: Measurements of volatile organic compounds in the Earth's atmosphere using proton-transfer-reaction mass spectrometry, Mass. Spectrom. Rev., 26, 223–257, 2007.
de Gouw, J., Warneke, C., Karl, T., Eerdekens, G., van der Veen, C., and Fall, R.: Sensitivity and specificity of atmospheric trace gas detection by proton-transfer-reaction mass spectrometry, Int. J. Mass Spectrom., 223/224, 365–382, 2003b.
de Gouw, J. A., Warneke, C., Stohl, A., Wollny, A. G., Brock, C. A., Cooper, O. R., Holloway, J. S., Trainer, M., Fehsenfeld, F. C., Atlas, E. L., Donnelly, S. G., Stroud, V., and Lueb, A.: Volatile organic compounds composition of merged and aged forest fire plumes from Alaska and western Canada, J. Geophys. Res., 111, D10303, https://doi.org/10.1029/2005JD006175, 2006.
Ehhalt, D. H. and Rohrer, F.: Dependence of the OH concentration on solar UV, J. Geophys. Res., 105, 3565–3571, 2000.
Fernandez, M. T., Williams, C., Mason, R. S., and Costa Cabral, B. J.: Experimental and theoretical proton affinity of limonene, J. Chem. Soc., Faraday Trans., 94, 1427–1430, 1998.
Geron, C., Rasmussen, R., Arnts, R. R., and Guenther, A.: A review and synthesis of monoterpene speciation from forests in the United States, Atmos. Environ., 34, 1761–1781, 2000.
Graedel, T. E.: Terpenoids in the atmosphere, Rev. Geophys., 17, 937–947, 1979.
Guenther, A. B., Zimmerman, P. R., Harley, P. C., Monson, R. K., and Fall, R.: Isoprene and monoterpene emission rate variability: model evaluations and sensitivity analyses, J. Geophys. Res., 98, D7, 12609–12617, 1993.
Hakola, H., Arey, J., Aschmann, S. M., and Atkinson, R.: Product formation from the gas-phase reactions of OH radicals and O3 with a series of monoterpenes, J. Atmos. Chem., 18, 75–102, 1994.
Hansel, A., Jordan, A., Holzinger, R., Prazeller, P., Vogel, W., and Lindinger, W.: Proton transfer reaction mass spectrometry: on-line trace gas analysis at the ppb level, Int. J. Mass. Spectrom. Ion Proc., 149/150, 609–619, 1995.
Hatakeyama, S., Izumi, K., Fukuyama, T., Akimoto, H., and Washida, N.: Reactions of OH with alpha-pinene and beta-pinene in air – estimate of global CO production from the atmospheric oxidation of terpenes, J. Geophys. Res., 96, D1, 947–958, 1991.
Hayward, S., Hewitt, C. N., Sartin, J. H., and Owen, S. M.: Performance characteristics and applications of a proton transfer reaction-mass spectrometer for measuring volatile organic compounds in ambient air, Environ. Sci. Technol., 36, 1554–1560, 2002.
Heiden, A. C., Kobel, K., Komenda, M., Koppmann, R., Shao, M., and Wildt, J.: Toluene emissions from plants, Geophys. Res. Lett., 26, 1283–1286, 1999.
Helmig, D., Klinger, L. F., Guenther, A., Vierling, L., Geron, C., and Zimmerman, P.: Biogenic volatile organic compound emissions (BVOCs) I. Identifications from three continental sites in the US, Chemosphere, 38, 2163–2187, 1998.
Hewitt, C. N., Hayward, S., and Tani, A.: The application of proton transfer reaction-mass spectrometry (PTR-MS) to the monitoring and analysis of volatile organic compounds in the atmosphere, J. Environ. Monit., 5, 1–7, 2003.
Holzinger, R., Sandoval-Soto, L., Rottenberger, S., Crutzen, P. J., and Kesselmeier, J.: Emissions of volatile organic compounds from Quercus ilex L. measured by Proton Transfer Reaction Mass Spectrometry under different environmental conditions, J. Geophys. Res., 105, 20573–20579, 2000.
Hurley, M. D., Sokolov, O., Wallington, T. J., Takekawa, H., Karasawa, M., Koltz, B., Barnes, I., and Becker, K. H.: Organic aerosol formation during the atmospheric degradation of toluene, Environ. Sci. Technol., 35, 1358–1366, 2001.
Justice, D., Deely, A. K., and Rubin, F.: New Hampshire Land Cover Assessment: Final Report, Complex Systems Research Center, University of New Hampshire, Durham, NH, Rep., 42pp., 2002.
Karl, T., Apel, E., Hodzic, A., Riemer, D. D., Blake, D. R., and Wiedinmyer, C.: Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity, Atmos. Chem. Phys., 9, 271–285, https://doi.org/10.5194/acp-9-271-2009, 2009.
Kato, S., Miyakawa, Y., Kaneko, T., and Kajii, Y.: Urban air measurements using PTR-MS in Tokyo area and comparison with GC-FID measurements, Int. J. Mass Spectrom., 235, 103–110, 2004.
Keck, L., Oeh, U., and Hoeschen, C.: Corrected equation for the concentrations in the drift tube of a proton transfer reaction-mass spectrometer (PTR-MS), Int. J. Mass Spectrom., 264, 92–95, 2007.
Kuster, W. C., Jobson, B. T., Karl, T., Riemer, D., Apel, E., Goldan, P. D., and Fehsenfeld, F. C.: Intercomparison of volatile organic carbon measurement techniques and data at La Porte during TexAQS2000 Air Quality Study, Environ. Sci. Technol., 38, 221–228, 2004.
Lee, A., Goldstein, A. H., Keywood, M. D., Gao, S., Varutbangkul, V., Bahreini, R., Ng., N. L., Flagan, R. C., and Seinfeld, J. H.: Gas-phase products and secondary aerosol yields from the ozonolysis of ten different terpenes, J. Geophys. Res., 111, D07302, https://doi.org/10.1029/2005JD006437, 2006a.
Lee, A., Goldstein, A. H., Kroll, J. H., Ng, N. L., Varutbangkul, V., Flagan, R. C., and Seinfeld, J. H.: Gas-phase products and secondary aerosol yields from the photooxidation of 16 different terpenes, J. Geophys. Res., 111, D17305, https://doi.org/10.1029/2006JD007050, 2006b.
Lide, D. R.: CRC Handbook of Chemistry and Physics, 88th ed., CRC Press, Boca Raton, FL, USA, 2008.
Liggio, J. and Li, S.-M.: Reactive uptake of pinonaldehyde on acidic aerosols, J. Geophys. Res., 111, D24303, https://doi.org/10.1029/2005JD006978, 2006.
Lindinger, W., Hansel, A., and Jordan, A.: On-line monitoring of volatile organic compounds at pptv levels by means of proton-transfer-reaction mass spectrometry (PTR-MS) – Medical applications, food control and environmental research, Int. J. Mass Spectrom., 173, 191–241, 1998a.
Lindinger, W., Hansel, H., and Jordan, A.: Proton-transfer-reaction mass spectrometry (PTR-MS): on-line monitoring of volatile organic compounds at pptv levels, Chem. Soc. Rev., 27, 347–354, 1998b.
Maleknia, S. D., Bell, T. L., and Adams, M. A.: PTR-MS analysis of reference and plant-emitted volatile organic compounds, Int. J. Mass Spectrom., 262, 203–210, 2007.
McFarland, M., Albritton, D. L., Fehsenfeld, F. C., Ferguson, E. E., and Schmeltekopf, A. L.: Flow-drift technique for ion mobility and ion-molecule reaction rate constant measurements. II. Positive ion reactions of N+, O+, and N2+ with O2 and O+ with N2 from thermal to 2 eV, J. Chem. Phys., 59, 6620–6628, 1973.
Ollinger, S. V., Aber, J. D., and Federer, C. A.: Estimating regional forest productivity and water yield using an ecosystem model linked to a GIS, Landscape Ecol., 13, 323–334, 1998.
Parrish, D. D., Stohl, A., Forster, C., Atlas, E. L., Blake, D. R., Goldan, P. D., Kuster, W. C., and de Gouw, J. A.: Effects of mixing on evolution of hydrocarbon ratios in the troposphere, J. Geophys. Res., 112, D10S34, https://doi.org/10.1029/2006JD007583, 2007.
Pinho, P. G., Pio, C. A., Carter, W. P. L., and Jenkin, M. E.: Evaluation of α- and β-pinene degradation in the detailed tropospheric chemistry mechanism, MCM v3.1, using environmental chamber data, J. Atmos. Chem., 57, 171–202, 2007.
Reissell, A., Aschmann, S. M., Atkinson, R., and Arey, J.: Products of the OH radical- and O3-initiated reactions with myrcene and ocimene, J. Geophys. Res., 107, D12, 4138, 10.1029/2001JD001234, 2002.
Rinne, J., Ruuskanen, R. M., Reissell, A., Taipale, R., Hakola, H., and Kulmala, M.: On-line PTR-MS measurements of atmospheric concentrations of volatile organic compounds in a European boreal forest ecosystem, Boreal Environ. Res., 10, 425–436, 2005.
Roberts, J. M., Fehsenfeld, F. C., Liu, S. C., Bollinger, M. J., Hahn, C., Albritton, D. L., and Sievers, R. E.: Measurements of aromatic hydrocarbon ratios and NOx concentrations in the rural troposphere: Estimates of air mass photochemical age and NOx removal rate, Atmos. Environ., 18, 2421–2432, 1984.
Roberts, J. M., Hahn, C. J., Fehsenfeld, F. C., Warnock, J. M., Albritton, D. L., and Sievers, R. E.: Monoterpene hydrocarbons in the nighttime troposphere, Environ. Sci. Tech., 19, 364–369, 1985.
Rogers, T. M., Grimsrud, E. P., Herndon, S. C., Jayne, J. T., Kolb, C. E., Allwine, E., Westberg, H., Lamb, B. K., Zavala, M., Molina, L. T., Molina, M. J., and Knighton, W. B.: On-road measurements of volatile organic compounds in the Mexico City metropolitan area using proton transfer reaction mass spectrometry, Int. J. Mass. Spectrom., 252, 26–37, 2006.
Rohrer, F. and Berresheim, H.: Strong correlation between levels of tropospheric hydroxyl radicals and solar ultraviolet radiation, Nature, 442, 184–187, 2006.
Russo, R. S., Zhou, Y., White, M. L., Mao, H., Talbot, R., and Sive, B. C.: Multi-year (2004–2008) record of nonmethane hydrocarbons and halocarbons in New England: seasonal variations and regional sources, Atmos. Chem. Phys., 10, 4909–4929, https://doi.org/10.5194/acp-10-4909-2010, 2010.
Schauer, J. J., Kleeman, M. J., Cass, G. R., and Simoneit, B. R. T.: Measurement of emissions from air pollution sources. 5. C1-C32 organic compounds from gasoline-powered motor vehicles, Environ. Sci. Technol., 36, 1169–1180, 2002.
Schoon, N., Amelynck, C., Vereecken, L., and Arijs, E.: A selected ion flow tube study of the reactions of H3O+, NO+ and O2+ with a series of monoterpenes, Int. J. Mass Spectrom., 229, 231–240, 2003.
Schoon, N, Amelynck, C., Vereecken, L., Coeckelberghs, H., and Arijs, E.: A selected ion flow tube study of the reactions of H3O+, NO+ and O2+ with some monoterpene oxidation products, Int. J. Mass Spectrom., 239, 7–16, 2004.
Singh, H. B. and Zimmerman, P. B.: Atmospheric distribution and sources of nonmethane hydrocarbons, in: Gaseous Pollutants: Characterization and Cycling, John Wiley & Sons, Inc., New York, NY, USA, 177–235, 1992.
Sive, B. C.: Atmospheric nonmethane hydrocarbons: Analytical methods and estimated hydroxyl radical concentrations, University of California, Irvine, Irvine, Ph.D. thesis, 1998.
Sive, B. C., Zhou, Y., Troop, D., Li, Y., Little, W., Wingenter, O. W., Russo, R. S., Varner, R. K., and Talbot, R. W.: Development of a cryogen-free concentration system for measurements of volatile organic compounds, Anal. Chem., 77, 6989–6998, https://doi.org/10.1021/ac0506231, 2005.
Smith, D. and Španel, P.: Selected Ion Flow Tube Mass Spectrometry (SIFT-MS) for on-line trace gas analysis, Mass Spectrom. Rev., 24, 661–700, 2005.
Španĕl, P. and Smith, D.: Selected ion flow tube studies of the reactions of H3O$^+$, NO$^+$, and O$_2^+$ with several aromatic and aliphatic hydrocarbons, Int. J. Mass Spectrom., 181, 1–10, 1998.
Steeghs, M., Bais, H. P., de Gouw, J., Goldan, P., Kuster, W., Northway, M., Fall, R., and Vivanco, J. M.: Proton-transfer-reaction mass spectrometry as a new tool for real time analysis of root-secreted volatile organic compounds in Arabidopsis, Plant. Physiol., 135, 47–58, 2004.
Talbot, R., Mao, H., and Sive, B. C.: Diurnal characteristics of surface level O3 and other important trace gases in New England, J. Geophys. Res., 110, D09307, https://doi.org/10.1029/2004JD005449, 2005.
Tan, C. Y. and Iglewicz, B.: Measurement-methods comparisons and linear statistical relationship, Technometrics, 41, 192–201, 1999.
Tani, A., Hayward, S., and Hewitt, C. N.: Measurement of monoterpenes and related compounds by proton transfer reaction-mass spectrometry (PTR-MS), Int. J. Mass Spectrom., 223/224, 561–578, 2003.
Tani, A., Hayward, S., Hansel, A., and Hewitt, C. N.: Effect of water vapor pressure on monoterpene measurements using proton transfer reaction-mass spectrometry (PTR-MS), Int. J. Mass. Spectrom., 239, 161–169, 2004.
Warneke, C., de Gouw, J., Kuster, W. C., Goldan, P. D., and Fall, R.: Validation of atmospheric VOC measurements by proton-transfer-reaction mass spectrometry using a gas-chromatographic preseparation method, Environ. Sci. Technol., 37, 2494–2501, 2003.
Warneke, C., McKeen, S. A., de Gouw, J. A., Goldan, P. D., Kuster, W. C., Holloway, J. S., Williams, E. J., Lerner, B. M., Parrish, D. D., Trainer, M., Fehsenfeld, F. C., Kato, S., Atlas, E. L., Baker, A., and Blank, D. R.: Determination of urban volatile organic compound emission ratios and comparison with an emissions database, J. Geophys. Res., 112, D10S47, https://doi.org/10.1029/2006JD007930, 2007.
Warneke, C., van der Veen, C., Luxembourg, S., de Gouw, J. A., and Kok, A.: Measurements of benzene and toluene in ambient air using proton-transfer-reaction mass spectrometry: calibration, humidity dependence, and field intercomparison, Int. J. Mass. Spectrom., 207, 167–182, 2001.
White, M. L., Russo, R. S., Zhou, Y., Ambrose, J. L., Haase, K., Frinak, E. K., Varner, R. K., Wingenter, O. W., Mao, H., Talbot, R., and Sive, B. C.: Are biogenic emissions a significant source of summertime atmospheric toluene in the rural Northeastern United States?, Atmos. Chem. Phys., 9, 81–92, https://doi.org/10.5194/acp-9-81-2009, 2009.
White, M. L., Russo, R. S., Zhou, Y., Mao, H., Varner, R. K., Ambrose, J., Veres, P., Wingenter, O. W., Haase, K., Stutz, J., Talbot, R., and Sive, B. C.: Volatile organic compounds in northern New England marine and continental environments during the ICARTT 2004 campaign, J. Geophys. Res., 113, D08S90, https://doi.org/10.1029/2007JD009161, 2008.
Wyche, K. P., Blake, R. S., Willis, K. A., Monks, P. S., and Ellis, A. M.: Differentiation of isobaric compounds using chemical ionization reaction mass spectrometry, Rapid Commun. Mass Spectrom., 19, 3356–3362, 2005.
Zhao, J. and Zhang, R.: Proton transfer reaction rate constants between hydronium ion (H3O$^{+})$ and volatile organic compounds, Atmos. Environ., 38, 2177–2185, 2004.
Zhou, Y., Varner, R. K., Russo, R. S., Wingenter, O. W., Haase, K. B., Talbot, R., and Sive, B. C.: Coastal water source of short-lived halocarbons in New England, J. Geophys. Res., 110, D21302, https://doi.org/10.1029/2004JD005603, 2005.
