scholarly journals Eddy covariance flux measurements of pollutant gases in urban Mexico City

2009 ◽  
Vol 9 (2) ◽  
pp. 7991-8034 ◽  
Author(s):  
E. Velasco ◽  
S. Pressley ◽  
R. Grivicke ◽  
E. Allwine ◽  
T. Coons ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Mexico City ◽  
Atmospheric Chemistry ◽  
Anthropogenic Activities ◽  
Flux Measurement ◽  
Proton Transfer Reaction ◽  
Surface Exchange ◽  
Emissions Inventory ◽  
Flux Measurements ◽  
Residential District

Abstract. Eddy covariance (EC) flux measurements of the atmosphere/surface exchange of gases over an urban area are a direct way to improve and evaluate emissions inventories, and, in turn, to better understand urban atmospheric chemistry and the role that cities play in regional and global chemical cycles. As part of the MCMA-2003 study, we demonstrated the feasibility of using eddy covariance techniques to measure fluxes of selected volatile organic compounds (VOCs) and CO2 from a residential district of Mexico City (Velasco et al., 2005a, b). During the MILAGRO/MCMA-2006 field campaign, a second flux measurement study was conducted in a different district of Mexico City to corroborate the 2003 flux measurements, to expand the number of species measured, and to obtain additional data for evaluation of the local emissions inventory. Fluxes of CO2 and olefins were measured by the conventional EC technique using an open path CO2 sensor and a Fast Isoprene Sensor calibrated with a propylene standard. In addition, fluxes of toluene, benzene, methanol and C2-benzenes were measured using a virtual disjunct EC method with a Proton Transfer Reaction Mass Spectrometer. The flux measurements were analyzed in terms of diurnal patterns and vehicular activity and were compared with the most recent gridded emissions inventory. In both studies, the results showed that the urban surface of Mexico City is a net source of CO2 and VOCs with significant contributions from vehicular traffic. Evaporative emissions from commercial and other anthropogenic activities were significant sources of toluene and methanol. The data show that the emissions inventory is in reasonable agreement with measured olefin and CO2 fluxes, while C2-benzenes and toluene emissions from evaporative sources are overestimated in the inventory. It appears that methanol emissions from mobile sources occur, but are not present in the mobile emissions inventory.

scholarly journals Eddy covariance flux measurements of pollutant gases in urban Mexico City

2009 ◽  
Vol 9 (19) ◽  
pp. 7325-7342 ◽  
Author(s):  
E. Velasco ◽  
S. Pressley ◽  
R. Grivicke ◽  
E. Allwine ◽  
T. Coons ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Mexico City ◽  
Atmospheric Chemistry ◽  
Anthropogenic Activities ◽  
Flux Measurement ◽  
Proton Transfer Reaction ◽  
Surface Exchange ◽  
Emissions Inventory ◽  
Flux Measurements ◽  
Local Emissions

Abstract. Eddy covariance (EC) flux measurements of the atmosphere/surface exchange of gases over an urban area are a direct way to improve and evaluate emissions inventories, and, in turn, to better understand urban atmospheric chemistry and the role that cities play in regional and global chemical cycles. As part of the MCMA-2003 study, we demonstrated the feasibility of using eddy covariance techniques to measure fluxes of selected volatile organic compounds (VOCs) and CO2 from a residential district of Mexico City (Velasco et al., 2005a, b). During the MILAGRO/MCMA-2006 field campaign, a second flux measurement study was conducted in a different district of Mexico City to corroborate the 2003 flux measurements, to expand the number of species measured, and to obtain additional data for evaluation of the local emissions inventory. Fluxes of CO2 and olefins were measured by the conventional EC technique using an open path CO2 sensor and a Fast Isoprene Sensor calibrated with a propylene standard. In addition, fluxes of toluene, benzene, methanol and C2-benzenes were measured using a virtual disjunct EC method with a Proton Transfer Reaction Mass Spectrometer. The flux measurements were analyzed in terms of diurnal patterns and vehicular activity and were compared with the most recent gridded local emissions inventory. In both studies, the results showed that the urban surface of Mexico City is a net source of CO2 and VOCs with significant contributions from vehicular traffic. Evaporative emissions from commercial and other anthropogenic activities were significant sources of toluene and methanol. The results show that the emissions inventory is in reasonable agreement with measured olefin and CO2 fluxes, while C2-benzenes and toluene emissions from evaporative sources are overestimated in the inventory. It appears that methanol emissions from mobile sources occur, but are not reported in the mobile emissions inventory.

scholarly journals PTR-TOF-MS eddy covariance measurements of isoprene and monoterpene fluxes from an eastern Amazonian rainforest

2020 ◽  
Vol 20 (12) ◽  
pp. 7179-7191 ◽  
Author(s):  
Chinmoy Sarkar ◽  
Alex B. Guenther ◽  
Jeong-Hoo Park ◽  
Roger Seco ◽  
Eliane Alves ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Atmospheric Chemistry ◽  
Sensible Heat Flux ◽  
Proton Transfer Reaction ◽  
Strongly Correlated ◽  
Mixing Ratios ◽  
Flux Measurements ◽  
Eddy Covariance Measurements ◽  
Emission Models ◽  
Tof Ms

Abstract. Biogenic volatile organic compounds (BVOCs) are important components of the atmosphere due to their contribution to atmospheric chemistry and biogeochemical cycles. Tropical forests are the largest source of the dominant BVOC emissions (e.g. isoprene and monoterpenes). In this study, we report isoprene and total monoterpene flux measurements with a proton transfer reaction time-of-flight mass spectrometer (PTR-TOF-MS) using the eddy covariance (EC) method at the Tapajós National Forest (2.857∘ S, 54.959∘ W), a primary rainforest in eastern Amazonia. Measurements were carried out from 1 to 16 June 2014, during the wet-to-dry transition season. During the measurement period, the measured daytime (06:00–18:00 LT) average isoprene mixing ratios and fluxes were 1.15±0.60 ppb and 0.55±0.71 mg C m−2 h−1, respectively, whereas the measured daytime average total monoterpene mixing ratios and fluxes were 0.14±0.10 ppb and 0.20±0.25 mg C m−2 h−1, respectively. Midday (10:00–14:00 LT) average isoprene and total monoterpene mixing ratios were 1.70±0.49 and 0.24±0.05 ppb, respectively, whereas midday average isoprene and monoterpene fluxes were 1.24±0.68 and 0.46±0.22 mg C m−2 h−1, respectively. Isoprene and total monoterpene emissions in Tapajós were correlated with ambient temperature and solar radiation. Significant correlation with sensible heat flux, SHF (r2=0.77), was also observed. Measured isoprene and monoterpene fluxes were strongly correlated with each other (r2=0.93). The MEGAN2.1 (Model of Emissions of Gases and Aerosols from Nature version 2.1) model could simulate most of the observed diurnal variations (r2=0.7 to 0.8) but declined a little later in the evening for both isoprene and total monoterpene fluxes. The results also demonstrate the importance of site-specific vegetation emission factors (EFs) for accurately simulating BVOC fluxes in regional and global BVOC emission models.

scholarly journals Chemically-resolved aerosol eddy covariance flux measurements in urban Mexico City during MILAGRO 2006

2012 ◽  
Vol 12 (16) ◽  
pp. 7809-7823 ◽  
Author(s):  
R. Zalakeviciute ◽  
M. L. Alexander ◽  
E. Allwine ◽  
J. L. Jimenez ◽  
B. T. Jobson ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Mexico City ◽  
Atmospheric Aerosols ◽  
Emission Inventory ◽  
Urban Landscape ◽  
Organic Aerosol ◽  
Emission Rates ◽  
Eddy Covariance Method ◽  
Emissions Inventory ◽  
Flux Measurements

Abstract. As part of the MILAGRO 2006 field campaign, the exchange of atmospheric aerosols with the urban landscape was measured from a tall tower erected in a heavily populated neighborhood of Mexico City. Urban submicron aerosol fluxes were measured using an eddy covariance method with a quadrupole aerosol mass spectrometer during a two week period in March, 2006. Nitrate and ammonium aerosol concentrations were elevated at this location near the city center compared to measurements at other urban sites. Significant downward fluxes of nitrate aerosol, averaging −0.2 μg m−2 s−1, were measured during daytime. The urban surface was not a significant source of sulfate aerosols. The measurements also showed that primary organic aerosol fluxes, approximated by hydrocarbon-like organic aerosols (HOA), displayed diurnal patterns similar to CO2 fluxes and anthropogenic urban activities. Overall, 47% of submicron organic aerosol emissions were HOA, 35% were oxygenated (OOA) and 18% were associated with biomass burning (BBOA). Organic aerosol fluxes were bi-directional, but on average HOA fluxes were 0.1 μg m−2 s−1, OOA fluxes were −0.03 μg m−2 s−1, and BBOA fluxes were −0.03 μg m−2 s−1. After accounting for size differences (PM1 vs PM2.5) and using an estimate of the black carbon component, comparison of the flux measurements with the 2006 gridded emissions inventory of Mexico City, showed that the daily-averaged total PM emission rates were essentially identical for the emission inventory and the flux measurements. However, the emission inventory included dust and metal particulate contributions, which were not included in the flux measurements. As a result, it appears that the inventory underestimates overall PM emissions for this location.

scholarly journals PTR-TOF-MS eddy covariance measurements of isoprene and monoterpene fluxes from an Eastern Amazonian rainforest

2020 ◽  
Author(s):  
Chinmoy Sarkar ◽  
Alex B. Guenther ◽  
Jeong-Hoo Park ◽  
Roger Seco ◽  
Eliane Alves ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Atmospheric Chemistry ◽  
Sensible Heat Flux ◽  
Proton Transfer Reaction ◽  
Strongly Correlated ◽  
Mixing Ratios ◽  
Flux Measurements ◽  
Eddy Covariance Measurements ◽  
Emission Models ◽  
Tof Ms

Abstract. Biogenic volatile organic compounds (BVOCs) are important components of the atmosphere due to their contribution to atmospheric chemistry and biogeochemical cycles. Tropical forests are the largest source of the dominant BVOC emissions (e.g. isoprene and monoterpenes). In this study, we report isoprene and total monoterpene flux measurements with a proton transfer reaction time-of-flight mass spectrometer (PTR-TOF-MS) using the eddy covariance (EC) method at the Tapajós National Forest (−2.857°S, −54.959°W), a primary rainforest in eastern Amazonia. Measurements were carried out from 1–16 June 2014, during the wet to dry transition season. During the measurement period, the measured daytime (06:00–18:00 LT) average isoprene mixing ratios and fluxes were 1.15 ± 0.60 ppb and 0.55 ± 0.71 mg C m−2 h−1, respectively, whereas the measured daytime average total monoterpenes mixing ratios and fluxes were 0.14 ± 0.10 ppb and 0.20 ± 0.25 mg C m−2 h−1, respectively. Midday (10:00–14:00 LT) average isoprene and total monoterpenes mixing ratios were 1.70 ± 0.49 ppb and 0.24 ± 0.05 ppb, respectively whereas midday average isoprene and monoterpene fluxes were 1.24 ± 0.68 mg C m−2 h−1 and 0.46 ± 0.22 mg C m−2 h−1, respectively. Isoprene and total monoterpene emissions in Tapajós were correlated with ambient temperature and solar radiation. Significant correlation with sensible heat flux, SHF (r2 = 0.77), was also observed. Measured isoprene and monoterpene fluxes were strongly correlated with each other (r2 = 0.93). The MEGAN2.1 model could simulate most of the observed diurnal variations (r2 = 0.7 to 0.8) but declined a little later in the evening for both isoprene and total monoterpene fluxes. The results also demonstrate the importance of site-specific vegetation emission factors (EFs) for accurately simulating BVOC fluxes in regional and global BVOC emission models.

scholarly journals Chemically-resolved aerosol eddy covariance flux measurements in urban Mexico City during MILAGRO 2006

2012 ◽  
Vol 12 (5) ◽  
pp. 11899-11939
Author(s):  
R. Zalakeviciute ◽  
M. L. Alexander ◽  
E. Allwine ◽  
J. L. Jimenez ◽  
B. T. Jobson ◽  
...  
Keyword(s):  
Eddy Covariance ◽  
Mexico City ◽  
Atmospheric Aerosols ◽  
Urban Landscape ◽  
Organic Aerosol ◽  
Eddy Covariance Method ◽  
Emissions Inventory ◽  
Aerosol Mass ◽  
Flux Measurements ◽  
Aerosol Emissions

Abstract. As part of the MILAGRO 2006 field campaign, the exchange of atmospheric aerosols with the urban landscape was measured from a tall tower erected in a heavily populated neighborhood of Mexico City. Urban submicron aerosol fluxes were measured using an eddy covariance method with a quadrupole aerosol mass spectrometer during a two week period in March 2006. Nitrate and ammonium aerosol concentrations were elevated at this location near the city center compared to measurements at other urban sites. Significant downward fluxes of nitrate aerosol, averaging −0.2 μg m−2 s−1, were measured during daytime. The urban surface was not a significant source of sulfate aerosols. The measurements also showed that primary organic aerosol fluxes, approximated by hydrocarbon-like organic aerosols (HOA), displayed diurnal patterns similar to CO2 fluxes and anthropogenic urban activities. Overall, 47% of submicron organic aerosol emissions were HOA, 35% were oxygenated (OOA) and 18% were associated with biomass burning (BBOA). Organic aerosol fluxes were bi-directional, but on average HOA fluxes were 0.09 μg m−2 s−1, OOA fluxes were −0.002 μg m−2 s−1, and BBOA fluxes were −0.03 μg m−2 s−1. The average diurnal flux results showed that the 2006 gridded emissions inventory of Mexico City underestimates mid-day and evening rush hour emissions of submicron aerosols for the monitored neighborhood, but averaged daily, the emission inventory and flux measurements for this location were in close agreement.

scholarly journals Eddy-covariance flux measurements with a weight-shift microlight aircraft

2012 ◽  
Vol 5 (7) ◽  
pp. 1699-1717 ◽  
Author(s):  
S. Metzger ◽  
W. Junkermann ◽  
M. Mauder ◽  
F. Beyrich ◽  
K. Butterbach-Bahl ◽  
...  
Keyword(s):  
Heat Flux ◽  
Eddy Covariance ◽  
Low Cost ◽  
Sensible Heat Flux ◽  
Flux Measurement ◽  
Wind Measurement ◽  
Airborne Measurements ◽  
Weight Shift ◽  
Flux Measurements

Abstract. The objective of this study is to assess the feasibility and quality of eddy-covariance flux measurements from a weight-shift microlight aircraft (WSMA). Firstly, we investigate the precision of the wind measurement (σu,v ≤ 0.09 m s−1, σw = 0.04 m s−1), the lynchpin of flux calculations from aircraft. From here, the smallest resolvable changes in friction velocity (0.02 m s−1), and sensible- (5 W m−2) and latent (3 W m−2) heat flux are estimated. Secondly, a seven-day flight campaign was performed near Lindenberg (Germany). Here we compare measurements of wind, temperature, humidity and respective fluxes between a tall tower and the WSMA. The maximum likelihood functional relationship (MLFR) between tower and WSMA measurements considers the random error in the data, and shows very good agreement of the scalar averages. The MLFRs for standard deviations (SDs, 2–34%) and fluxes (17–21%) indicate higher estimates of the airborne measurements compared to the tower. Considering the 99.5% confidence intervals, the observed differences are not significant, with exception of the temperature SD. The comparison with a large-aperture scintillometer reveals lower sensible heat flux estimates at both tower (−40 to −25%) and WSMA (−25–0%). We relate the observed differences to (i) inconsistencies in the temperature and wind measurement at the tower and (ii) the measurement platforms' differing abilities to capture contributions from non-propagating eddies. These findings encourage the use of WSMA as a low cost and highly versatile flux measurement platform.

scholarly journals Design of the AmeriFlux Portable Eddy Covariance System and Uncertainty Analysis of Carbon Measurements

2007 ◽  
Vol 24 (8) ◽  
pp. 1389-1406 ◽  
Author(s):  
T. W. Ocheltree ◽  
H. W. Loescher
Keyword(s):  
Eddy Covariance ◽  
Spatial Scales ◽  
Flux Measurement ◽  
Field Measurements ◽  
Quality Control Laboratory ◽  
Flux Measurements ◽  
Eddy Covariance System ◽  
Uncertainty Analyses ◽  
Infrared Gas Analyzer ◽  
Ambient Co2

Abstract The AmeriFlux network continues to improve the understanding of carbon, water, and energy fluxes across temporal and spatial scales. The network includes ∼120 research sites that contribute to the understanding of processes within and among ecosystems. To improve the networks ability and confidence to synthesize data across multiple sites, the AmeriFlux quality assurance and quality control laboratory was established to reduce the within- and among-site uncertainties. This paper outlines the design of the portable eddy covariance system (PECS) and subsequent data processing procedures used for site comparisons. Because the PECS makes precision measurements of atmospheric CO2, the authors also present the results of uncertainty analyses in determining the polynomials for an infrared gas analyzer, estimating the CO2 in secondary standards, and estimating ambient CO2 in field measurements. Under field conditions, drift in the measurement of CO2 increased the uncertainty in flux measurements across 7 days by 5% and was not dependent on the magnitude or direction of the flux. The maximum relative flux measurement error for unstable conditions was 10.03 μmol CO2 m−2 s−1.

scholarly journals Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity

2008 ◽  
Vol 8 (4) ◽  
pp. 14273-14309 ◽  
Author(s):  
T. Karl ◽  
E. Apel ◽  
A. Hodzic ◽  
D. Riemer ◽  
D. Blake ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Eddy Covariance ◽  
Organic Compounds ◽  
Mexico City ◽  
Biomass Burning ◽  
Minor Role ◽  
Industrial Emissions ◽  
Tertiary Butyl ◽  
Volatile Organic ◽  
Flux Measurements

Abstract. Toluene and benzene are used for assessing the ability to measure disjunct eddy covariance (DEC) fluxes of Volatile Organic Compounds (VOC) using Proton Transfer Reaction Mass Spectrometry (PTR-MS) on aircraft. Statistically significant correlation between vertical wind speed and mixing ratios suggests that airborne VOC eddy covariance (EC) flux measurements using PTR-MS are feasible. City-average midday toluene and benzene fluxes are calculated to be on the order of 15.5±4.0 mg/m2/h and 4.7±2.3 mg/m2/h respectively. These values argue for an underestimation of toluene and benzene emissions in current inventories used for the Mexico City Metropolitan Area (MCMA). Wavelet analysis of instantaneous toluene and benzene measurements during city overpasses is tested as a tool to assess surface emission heterogeneity. High toluene to benzene flux ratios above an industrial district (e.g. 10–15) including the International airport (e.g. 3–5) and a mean flux (concentration) ratio of 3.2±0.5 (3.9±0.3) across Mexico City indicate that evaporative fuel and industrial emissions play an important role for the prevalence of aromatic compounds. Based on a tracer model, which was constrained by BTEX (Benzene/Toluene/Ethylbenzene/m,p,o-Xylenes) compound concentration ratios, the fuel marker methyl-tertiary-butyl-ether (MTBE) and the biomass burning marker acetonitrile (CH3CN), we show that a combination of industrial, evaporative fuel, and exhaust emissions account for >90% of all BTEX sources. Our observations suggest that biomass burning emissions play a minor role for the abundance of BTEX compounds (0–10%) in the MCMA.

scholarly journals Mixing ratios and eddy covariance flux measurements of volatile organic compounds from an urban canopy (Manchester, UK)

2008 ◽  
Vol 8 (1) ◽  
pp. 245-284 ◽  
Author(s):  
B. Langford ◽  
B. Davison ◽  
E. Nemitz ◽  
C. N. Hewitt
Keyword(s):  
Volatile Organic Compounds ◽  
Eddy Covariance ◽  
Organic Compounds ◽  
Urban Canopy ◽  
Proton Transfer Reaction ◽  
Anthropogenic Sources ◽  
Emissions Inventory ◽  
Mixing Ratios ◽  
Volatile Organic ◽  
The Individual

Abstract. Concentrations and fluxes of six volatile organic compounds (VOC) were measured above the city of Manchester (UK) during the summer of 2006. A proton transfer reaction-mass spectrometer was used for the measurement of concentrations, and fluxes were calculated using both the disjunct and the virtual disjunct eddy covariance techniques. The two flux systems, which operated in alternate half hours, showed reasonable agreement, with R2 values ranging between 0.2 and 0.8 for the individual analytes. On average, fluxes measured in the disjunct mode were lower than those measured in the virtual mode by approximately 19%, of which at least 8% can be attributed to the differing measurement frequencies of the two systems and the subsequent attenuation of high frequency flux contributions. Observed fluxes are thought to be largely controlled by anthropogenic sources, with vehicle emissions the major contributor. However both evaporative and biogenic emissions may account for a fraction of the isoprene present. Fluxes of the oxygenated compounds were highest on average, ranging between 60–89 μg m−2 h−1, whereas the fluxes of aromatic compounds were lower, between 19–42 μg m−2 h−1. The observed fluxes of benzene were up-scaled to give a city wide emission estimate which was found to be significantly lower than that of the National Atmospheric Emissions Inventory (NAEI).

scholarly journals Chemical sensor resolution requirements for near-surface measurements of turbulent fluxes

2011 ◽  
Vol 11 (11) ◽  
pp. 5263-5275 ◽  
Author(s):  
M. D. Rowe ◽  
C. W. Fairall ◽  
J. A. Perlinger
Keyword(s):  
Eddy Covariance ◽  
Field Experiments ◽  
Chemical Sensor ◽  
Flux Measurement ◽  
Similarity Function ◽  
Atmospheric Parameter ◽  
Transfer Velocity ◽  
Surface Exchange ◽  
Near Surface ◽  
Sensor Resolution

Abstract. Businger and Delany (1990) presented an approach to estimate the sensor resolution required to limit the contribution of the uncertainty in the chemical concentration measurement to uncertainty in the flux measurement to 10 % for eddy covariance, gradient, and relaxed eddy accumulation flux measurement methods. We describe an improvement to their approach to estimate required sensor resolution for the covariance method, and include disjunct eddy covariance. In addition, we provide data to support selection of a form for the dimensionless scalar standard deviation similarity function based on observations of the variance of water vapor fluctuations from recent field experiments. We also redefine the atmospheric parameter of Businger and Delany in a more convenient, dimensionless form. We introduce a "chemical parameter" based on transfer velocity parameterizations. Finally, we provide examples in which the approach is applied to measurement of carbon dioxide, dimethylsulfide, and hexachlorobenzene fluxes over water. The information provided here will be useful to plan field measurements of atmosphere-surface exchange fluxes of trace gases.

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