scholarly journals Quantifying burning efficiency in megacities using the NO<sub>2</sub>∕CO ratio from the Tropospheric Monitoring Instrument (TROPOMI)

2020 ◽  
Vol 20 (17) ◽  
pp. 10295-10310 ◽  
Author(s):  
Srijana Lama ◽  
Sander Houweling ◽  
K. Folkert Boersma ◽  
Henk Eskes ◽  
Ilse Aben ◽  
...  
Keyword(s):  
Los Angeles ◽  
Mexico City ◽  
Atmospheric Chemistry ◽  
Combustion Efficiency ◽  
Air Quality Monitoring ◽  
Monitoring Networks ◽  
Emission Ratio ◽  
Efficient Combustion ◽  
Rotation Methods ◽  
Emission Ratios

Abstract. This study investigates the use of co-located nitrogen dioxide (NO2) and carbon monoxide (CO) retrievals from the TROPOMI satellite to improve the quantification of burning efficiency and emission factors (EFs) over the megacities of Tehran, Mexico City, Cairo, Riyadh, Lahore, and Los Angeles. Efficient combustion is characterized by high NOx (NO+NO2) and low CO emissions, making the NO2∕CO ratio a useful proxy for combustion efficiency (CE). The local enhancement of CO and NO2 above megacities is well captured by TROPOMI at short averaging times compared with previous satellite missions. In this study, the upwind background and plume rotation methods are used to investigate the accuracy of satellite-derived ΔNO2∕ΔCO ratios. The column enhancement ratios derived using these two methods vary by 5 % to 20 % across the selected megacities. TROPOMI-derived column enhancement ratios are compared with emission ratios from the EDGAR v4.3.2 (Emission Database for Global Atmospheric Research v4.3.2) and the MACCity (Monitoring Atmospheric Chemistry and Climate and CityZen) 2018 emission inventories. TROPOMI correlates strongly (r=0.85 and 0.7) with EDGAR and MACCity, showing the highest emission ratio for Riyadh and lowest emission ratio for Lahore. However, inventory-derived emission ratios are 60 % to 85 % higher than TROPOMI column enhancement ratios across the six megacities. The short lifetime of NO2 and the different vertical sensitivity of TROPOMI NO2 and CO explain most of this difference. We present a method to translate TROPOMI-retrieved column enhancement ratios into corresponding emission ratios, thereby accounting for these influences. Except for Los Angeles and Lahore, TROPOMI-derived emission ratios are close (within 10 % to 25 %) to MACCity values. For EDGAR, however, emission ratios are ∼65 % higher for Cairo and 35 % higher for Riyadh. For Los Angeles, EDGAR and MACCity are a factor of 2 and 3 higher than TROPOMI respectively. The air quality monitoring networks in Los Angeles and Mexico City are used to validate the use of TROPOMI. For Mexico City and Los Angeles, these measurements are consistent with TROPOMI-derived emission ratios, demonstrating the potential of TROPOMI with respect to monitoring burning efficiency.

scholarly journals Quantifying burning efficiency in Megacities using NO<sub>2</sub> / CO ratio from the Tropospheric Monitoring Instrument (TROPOMI)

2019 ◽  
Author(s):  
Srijana Lama ◽  
Sander Houweling ◽  
K. Folkert Boersma ◽  
Ilse Aben ◽  
Hugo A. C. Denier van der Gon ◽  
...  
Keyword(s):  
Los Angeles ◽  
Mexico City ◽  
Quality Monitoring ◽  
Emission Inventories ◽  
Air Quality Monitoring ◽  
Monitoring Networks ◽  
Local Enhancement ◽  
Emission Ratio ◽  
Rotation Methods ◽  
Emission Ratios

Abstract. This study investigates the use of co-located NO2 and CO retrievals from the TROPOMI satellite to improve the quantification of burning efficiency and emission factors over the mega-cities of Tehran, Mexico City, Cairo, Riyadh, Lahore and Los Angeles. Local enhancement of CO and NO2 above megacities are well captured by TROPOMI at relatively short averaging times. In this study, the Upwind Background and Plume rotation methods are used to investigate the accuracy of satellite derived ∆NO2 / ∆CO ratios. The column enhancement ratios derived using these two methods vary by 5 to 30 % across the selected megacities. TROPOMI derived column enhancement ratios are compared with emission ratios from the EDGAR v4.3.2 and MACCity, 2018 emission inventories. TROPOMI correlates strongly (r = 0.85 and 0.7) with EDGAR and MACCity showing the highest emission ratio for Riyadh and lowest for Lahore. However, inventory derived emission ratios are higher by 60 to 80 % compared to TROPOMI column enhancement ratios across the six megacities. The short lifetime of NO2 and different vertical sensitivity of TROPOMI NO2 and CO explain most of this difference. We present a method to translate TROPOMI retrieved column enhancement ratios into corresponding emission ratio, accounting for these influences. Except for Los Angeles, TROPOMI derived emission ratios are close (within 10 to 25 %) to MACCity. For EDGAR, however, emission ratios are higher by ~80 % for Cairo, 30 to 45 % for Riyadh and ~70 % for Los Angeles. The air quality monitoring networks in Los Angeles and Mexico City are used to validate the use of TROPOMI. Over Mexico City, these measurements are consistent with TROPOMI, EDGAR and MACCIty derived emission ratios. For Los Angeles, however, EDGAR and MACCity are higher by a factor 5 compared to TROPOMI. The ground-based measurements are consistent with a poorer burning efficiency in Los Angeles as inferred from TROPOMI, demonstrating its potential to monitor burning efficiency.

scholarly journals Gridded global surface ozone metrics for atmospheric chemistry model evaluation

2015 ◽  
Vol 8 (2) ◽  
pp. 603-647 ◽  
Author(s):  
E. D. Sofen ◽  
D. Bowdalo ◽  
M. J. Evans ◽  
F. Apadula ◽  
P. Bonasoni ◽  
...  
Keyword(s):  
Air Quality ◽  
Atmospheric Chemistry ◽  
Model Evaluation ◽  
Climate Model ◽  
Surface Ozone ◽  
Quality Monitoring ◽  
Air Quality Monitoring ◽  
Monitoring Networks ◽  
Chemistry Research ◽  
Consistent Manner

Abstract. The concentration of ozone at the Earth's surface is measured at many locations across the globe for the purposes of air quality monitoring and atmospheric chemistry research. We have brought together all publicly available surface ozone observations from online databases from the modern era to build a consistent dataset for the evaluation of chemical transport and chemistry-climate (Earth System) models for projects such as the Chemistry-Climate Model Initiative and Aer-Chem-MIP. From a total dataset of approximately 6600 sites and 500 million hourly observations from 1971–2015, approximately 2200 sites and 200 million hourly observations pass screening as high-quality sites in regional background locations that are appropriate for use in global model evaluation. There is generally good data volume since the start of air quality monitoring networks in 1990 through 2013. Ozone observations are biased heavily toward North America and Europe with sparse coverage over the rest of the globe. This dataset is made available for the purposes of model evaluation as a set of gridded metrics intended to describe the distribution of ozone concentrations on monthly and annual timescales. Metrics include the moments of the distribution, percentiles, maximum daily eight-hour average (MDA8), SOMO35, AOT40, and metrics related to air quality regulatory thresholds. Gridded datasets are stored as netCDF-4 files and are available to download from the British Atmospheric Data Centre (doi:10.5285/08fbe63d-fa6d-4a7a-b952-5932e3ab0452). We provide recommendations to the ozone measurement community regarding improving metadata reporting to simplify ongoing and future efforts in working with ozone data from disparate networks in a consistent manner.

Quantifying burning efficiency in Megacities using NO2/CO ratio from the Tropospheric Monitoring Instrument (TROPOMI)

2020 ◽  
Author(s):  
Srijana Lama ◽  
Sander Houweling ◽  
Folkert Boersma ◽  
Ilse Aben ◽  
Hugo Denier van der Gon ◽  
...  
Keyword(s):  
Air Quality ◽  
Los Angeles ◽  
Atmospheric Chemistry ◽  
European Space Agency ◽  
Monitoring Network ◽  
Emission Factors ◽  
Rapid Urbanization ◽  
Global Emission ◽  
The Impact ◽  
Emission Ratios

&lt;p&gt;Economic development and rapid urbanization have increased the consumption of fossil fuel in megacities degrading the local air quality. Burning efficiency is a major factor determining the impact of fuel burning on the environment. It varies with environmental conditions and influences the ratio at which pollutants are emitted, as expressed by the emission factor. Emission factors are an important source of uncertainty in global emission inventories.&lt;/p&gt;&lt;p&gt;To improve the quantification of burning efficiency and emission factors, this study investigates co-located NO&lt;sub&gt;2&lt;/sub&gt; and CO satellite retrievals from TROPOMI over the megacities of Tehran, Mexico City, Cairo, Riyadh, Lahore and Los Angeles. The TROPOMI instrument was successfully launched by the European Space Agency on 13 October, 2017. It measures atmospheric trace gases with daily coverage and a spatial resolution of 7x7 km&lt;sup&gt;2&lt;/sup&gt;. At this resolution, TROPOMI detects hotspots of CO and NO&lt;sub&gt;2&lt;/sub&gt; pollution over megacities in single satellite overpasses. The Upwind Background and Plume rotation methods are applied to quantify and evaluate TROPOMI derived &amp;#8710;NO&lt;sub&gt;2&lt;/sub&gt;/&amp;#8710;CO ratios. TROPOMI derived &amp;#8710;NO&lt;sub&gt;2&lt;/sub&gt;/&amp;#8710;CO ratios show a strong correlation (r = 0.85 and 0.7) with emission ratios from the Emission Database for Global Atmospheric Research (EDGAR v4.3.2) and Monitoring Atmospheric Chemistry and Climate and CityZen (MACCity) 2018, with the highest ratio for Riyadh and lowest for Lahore. Inventory-derived emission ratios are larger than TROPOMI-derived total column ratios by 60 to 80%. As we will show, this can largely be explained by the limited lifetime of NO&lt;sub&gt;2&lt;/sub&gt; and the different vertical sensitivity of the TROPOMI NO&lt;sub&gt;2 &lt;/sub&gt;and CO column retrievals. Taking this into account, TROPOMI retrieved emission ratios are generally within 10 to 25% of MACCity. However, larger differences, up to 80%, are found with EDGAR. For Los Angeles, both inventories overestimate NO2/CO ratios compared with TROPOMI. Validation using the air quality monitoring network of Los Angeles supports the lower &amp;#8710;NO&lt;sub&gt;2&lt;/sub&gt;/&amp;#8710;CO ratios inferred from TROPOMI, indicating that burning efficiencies in Los Angeles are indeed poorer than indicated by the inventories.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;&amp;#160;&lt;/strong&gt;&lt;/p&gt;

scholarly journals Airborne measurements of trace gas and aerosol particle emissions from biomass burning in Amazonia

2005 ◽  
Vol 5 (11) ◽  
pp. 2989-3002 ◽  
Author(s):  
P. Guyon ◽  
G. P. Frank ◽  
M. Welling ◽  
D. Chand ◽  
P. Artaxo ◽  
...  
Keyword(s):  
Large Scale ◽  
Particle Number ◽  
Aerosol Particles ◽  
Secondary Growth ◽  
Combustion Efficiency ◽  
Vertical Transport ◽  
Airborne Measurements ◽  
Sampling Campaign ◽  
Wide Range ◽  
Emission Ratios

Abstract. As part of the LBA-SMOCC (Large-Scale Biosphere-Atmosphere Experiment in Amazonia - Smoke, Aerosols, Clouds, Rainfall, and Climate) 2002 campaign, we studied the emission of carbon monoxide (CO), carbon dioxide (CO2), and aerosol particles from Amazonian deforestation fires using an instrumented aircraft. Emission ratios for aerosol number (CN) relative to CO (ERCN/CO) fell in the range 14-32 cm-3 ppb-1 in most of the investigated smoke plumes. Particle number emission ratios have to our knowledge not been previously measured in tropical deforestation fires, but our results are in agreement with values usually found from tropical savanna fires. The number of particles emitted per amount biomass burned was found to be dependent on the fire conditions (combustion efficiency). Variability in ERCN/CO between fires was similar to the variability caused by variations in combustion behavior within each individual fire. This was confirmed by observations of CO-to-CO2 emission ratios (ERCO/CO2), which stretched across the same wide range of values for individual fires as for all the fires observed during the sampling campaign, reflecting the fact that flaming and smoldering phases are present simultaneously in deforestation fires. Emission factors (EF) for CO and aerosol particles were computed and a correction was applied for the residual smoldering combustion (RSC) fraction of emissions that are not sampled by the aircraft, which increased the EF by a factor of 1.5-2.1. Vertical transport of smoke from the boundary layer (BL) to the cloud detrainment layer (CDL) and the free troposphere (FT) was found to be a very common phenomenon. We observed a 20% loss in particle number as a result of this vertical transport and subsequent cloud processing, attributable to in-cloud coagulation. This small loss fraction suggests that this mode of transport is very efficient in terms of particle numbers and occurs mostly via non-precipitating clouds. The detrained aerosol particles released in the CDL and FT were larger than in the unprocessed smoke, mostly due to coagulation and secondary growth, and therefore more efficient at scattering radiation and nucleating cloud droplets. This process may have significant atmospheric implications on a regional and larger scale.

Mexican Migration and the Social Space of Postmodernism

1991 ◽  
Vol 1 (1) ◽  
pp. 8-23
Author(s):  
Roger Rouse
Keyword(s):  
United States ◽  
Los Angeles ◽  
Mexico City ◽  
Latin American ◽  
Social Space ◽  
The United States ◽  
Mexican Migration ◽  
Single Word ◽  
The Social ◽  
Made In

In a hidden sweatshop in downtown Los Angeles, Asian and Latino migrants produce automobile parts for a factory in Detroit. As the parts leave the production line, they are stamped “Made in Brazil.” In a small village in the heart of Mexico, a young woman at her father’s wake wears a black T-shirt sent to her by a brother in the United States. The shirt bears a legend that some of the mourners understand but she does not. It reads, “Let’s Have Fun Tonight!” And on the Tijuana-San Diego border, Guillermo Gómez-Peña, a writer originally from Mexico City, reflects on the time he has spent in what he calls “the gap between two worlds”: “Today, eight years after my departure, when they ask me for my nationality or ethnic identity, I cannot answer with a single word, for my ‘identity’ now possesses multiple repertoires: I am Mexican but I am also Chicano and Latin American. On the border they call me ‘chilango’ or ‘mexiquillo’; in the capital, ‘pocho’ or ‘norteno,’ and in Spain ‘sudaca.’… My companion Emily is Anglo-Italian but she speaks Spanish with an Argentinian accent. Together we wander through the ruined Babel that is our American postmodemity.”

scholarly journals Analysis and optimal design of air quality monitoring networks using a variational approach

Tellus B ◽  
2015 ◽  
Vol 67 (1) ◽  
pp. 25385 ◽  
Author(s):  
Adolfo Henriquez ◽  
Axel Osses ◽  
Laura Gallardo ◽  
Melisa Diaz Resquin
Keyword(s):  
Air Quality ◽  
Optimal Design ◽  
Variational Approach ◽  
Quality Monitoring ◽  
Air Quality Monitoring ◽  
Monitoring Networks

scholarly journals Evaluation of global EMEP MSC-W (rv4.34) WRF (v3.9.1.1) model surface concentrations and wet deposition of reactive N and S with measurements

2021 ◽  
Vol 14 (11) ◽  
pp. 7021-7046
Author(s):  
Yao Ge ◽  
Mathew R. Heal ◽  
David S. Stevenson ◽  
Peter Wind ◽  
Massimo Vieno
Keyword(s):  
North America ◽  
Southeast Asia ◽  
East Asia ◽  
Atmospheric Chemistry ◽  
Wet Deposition ◽  
Global Analysis ◽  
Monitoring Networks ◽  
Model Framework ◽  
Annual Total ◽  
Model Measurement

Abstract. Atmospheric pollution has many profound effects on human health, ecosystems, and the climate. Of concern are high concentrations and deposition of reactive nitrogen (Nr) species, especially of reduced N (gaseous NH3, particulate NH4+). Atmospheric chemistry and transport models (ACTMs) are crucial to understanding sources and impacts of Nr chemistry and its potential mitigation. Here we undertake the first evaluation of the global version of the EMEP MSC-W ACTM driven by WRF meteorology (1∘×1∘ resolution), with a focus on surface concentrations and wet deposition of N and S species relevant to investigation of atmospheric Nr and secondary inorganic aerosol (SIA). The model–measurement comparison is conducted both spatially and temporally, covering 10 monitoring networks worldwide. Model simulations for 2010 compared use of both HTAP and ECLIPSEE (ECLIPSE annual total with EDGAR monthly profile) emissions inventories; those for 2015 used ECLIPSEE only. Simulations of primary pollutants are somewhat sensitive to the choice of inventory in places where regional differences in primary emissions between the two inventories are apparent (e.g. China) but are much less sensitive for secondary components. For example, the difference in modelled global annual mean surface NH3 concentration using the two 2010 inventories is 18 % (HTAP: 0.26 µg m−3; ECLIPSEE: 0.31 µg m−3) but is only 3.5 % for NH4+ (HTAP: 0.316 µg m−3; ECLIPSEE: 0.305 µg m−3). Comparisons of 2010 and 2015 surface concentrations between the model and measurements demonstrate that the model captures the overall spatial and seasonal variations well for the major inorganic pollutants NH3, NO2, SO2, HNO3, NH4+, NO3-, and SO42- and their wet deposition in East Asia, Southeast Asia, Europe, and North America. The model shows better correlations with annual average measurements for networks in Southeast Asia (mean R for seven species: R7‾=0.73), Europe (R7‾=0.67), and North America (R7‾=0.63) than in East Asia (R5‾=0.35) (data for 2015), which suggests potential issues with the measurements in the latter network. Temporally, both model and measurements agree on higher NH3 concentrations in spring and summer and lower concentrations in winter. The model slightly underestimates annual total precipitation measurements (by 13 %–45 %) but agrees well with the spatial variations in precipitation in all four world regions (0.65–0.94 R range). High correlations between measured and modelled NH4+ precipitation concentrations are also observed in all regions except East Asia. For annual total wet deposition of reduced N, the greatest consistency is in North America (0.75–0.82 R range), followed by Southeast Asia (R=0.68) and Europe (R=0.61). Model–measurement bias varies between species in different networks; for example, bias for NH4+ and NO3- is largest in Europe and North America and smallest in East Asia and Southeast Asia. The greater uniformity in spatial correlations than in biases suggests that the major driver of model–measurement discrepancies (aside from differing spatial representativeness and uncertainties and biases in measurements) are shortcomings in absolute emissions rather than in modelling the atmospheric processes. The comprehensive evaluations presented in this study support the application of this model framework for global analysis of current and potential future budgets and deposition of Nr and SIA.

scholarly journals Observations of atmospheric <sup>14</sup>CO<sub>2</sub> at Anmyeondo GAW station, South Korea: implications for fossil fuel CO<sub>2</sub> and emission ratios

2020 ◽  
Vol 20 (20) ◽  
pp. 12033-12045
Author(s):  
Haeyoung Lee ◽  
Edward J. Dlugokencky ◽  
Jocelyn C. Turnbull ◽  
Sepyo Lee ◽  
Scott J. Lehman ◽  
...  
Keyword(s):  
South Korea ◽  
Sulfur Hexafluoride ◽  
Fossil Fuel ◽  
Combustion Efficiency ◽  
Mean Value ◽  
Asian Continent ◽  
Air Masses ◽  
Air Samples ◽  
Carbon Dioxide Co2 ◽  
Emission Ratios

Abstract. To understand the Korean Peninsula's carbon dioxide (CO2) emissions and sinks as well as those of the surrounding region, we used 70 flask-air samples collected during May 2014 to August 2016 at Anmyeondo (AMY; 36.53∘ N, 126.32∘ E; 46 m a.s.l.) World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) station, located on the west coast of South Korea, for analysis of observed 14C in atmospheric CO2 as a tracer of fossil fuel CO2 contribution (Cff). Observed 14C ∕ C ratios in CO2 (reported as Δ values) at AMY varied from −59.5 ‰ to 23.1 ‰, with a measurement uncertainty of ±1.8 ‰. The derived mean value Cff of (9.7±7.8) µmol mol−1 (1σ) is greater than that found in earlier observations from Tae-Ahn Peninsula (TAP; 36.73∘ N, 126.13∘ E; 20 m a.s.l., 28 km away from AMY) of (4.4±5.7) µmol mol−1 from 2004 to 2010. The enhancement above background mole fractions of sulfur hexafluoride (Δx(SF6)) and carbon monoxide (Δx(CO)) correlate strongly with Cff (r>0.7) and appear to be good proxies for fossil fuel CO2 at regional and continental scales. Samples originating from the Asian continent had greater Δx(CO) : Cff(RCO) values, (29±8) to (36±2) nmol µmol−1, than in Korean Peninsula local air ((8±2) nmol µmol−1). Air masses originating in China showed (1.6±0.4) to (2.0±0.1) times greater RCO than a bottom-up inventory, suggesting that China's CO emissions are underestimated in the inventory, while observed RSF6 values are 2–3 times greater than inventories for both China and South Korea. However, RCO values derived from both inventories and observations have decreased relative to previous studies, indicating that combustion efficiency is increasing in both China and South Korea.

A Future Multi-Platform Atmospheric Chemistry Measurement Campaign to Study Oxidation in Mixed Anthropogenic-Biogenic Air Masses

2021 ◽  
Author(s):  
Christopher Cantrell ◽  
Vincent Michoud ◽  
Paola Formenti ◽  
Jean-Francois Doussin ◽  
Stephanie Alhajj Moussa ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Los Angeles ◽  
Organic Compounds ◽  
Atmospheric Chemistry ◽  
Vapor Pressures ◽  
Air Masses ◽  
Measurement Campaign ◽  
Secondary Species ◽  
Volatile Organic ◽  
Urban Plumes

&lt;p&gt;It is well known that the high population density of urban regions leads to significant degradation of the quality of the air because of the emissions of pollutants that are by-products of energy production, transportation, and industry. The composition and chemistry of urban air has been studied for many decades and these studies have led to detailed understanding of the factors controlling, for example, the formation of ozone, peroxyacetyl nitrate and other secondary species. In the last 20 to 30 years, significant progress has been made in reducing emissions of volatile organic compounds (VOCs) and oxides of nitrogen (NO&lt;sub&gt;x&lt;/sub&gt;) in urban atmospheres. Substantial reductions in the abundance of secondary compounds, though, have been more elusive.&lt;/p&gt;&lt;p&gt;Research has continued to reveal more and more details of the complex processes involved in the atmospheric degradation of wide varieties of volatile organic compounds (VOCs) of anthropogenic and biospheric (BVOCs) origins. BVOCs include isoprene, monoterpenes and sesquiterpenes, and oxygenated VOCs (OVOCs, such as small alcohols). Emissions of BVOCs depend on several factors such as plant or tree species, temperature, and photosynthetically active radiation. They consist almost exclusively of unsaturated compounds with chemistry somewhat different from those of typical urban organic compound emissions. Oxidation of VOCs can lead to molecules of low volatility that are prone to uptake into the aerosol phase.&lt;/p&gt;&lt;p&gt;Recent studies conducted in megacities such as Paris, Mexico City, Los Angeles and those in China have led to significant advances in our understanding of the chemical evolution of urban plumes. However, important scientific questions remain on how mixing of anthropogenic and biogenic air masses modifies the composition of urban plumes and hence their impacts. Indeed, the proximity of cites to areas of strong biogenic emissions is not unusual. Many major cities at mid-latitudes are surrounded by forested areas.&lt;/p&gt;&lt;p&gt;ACROSS (Atmospheric ChemistRy Of the Suburban foreSt) is an integrative, innovative, multi-scale project awarded under the &amp;#8220;Make Our Planet Great Again&amp;#8221; (MOPGA) framework that seeks to definitively improve understanding of the impacts of mixing urban and biogenic air masses on the oxidation of atmospheric VOCs. The ACROSS working hypothesis is that this leads to changes in the production of oxygenated VOCs whose properties (e.g. vapor pressures) alter their importance in incorporation into SOA and their roles in production of ozone and other secondary species. Changes are also expected in the efficiency of radical recycling affecting the atmospheric oxidative capacity. Particularly important is NO&lt;sub&gt;x&lt;/sub&gt; transport to suburban biogenic environments and the resulting modification of key chemical processes.&lt;/p&gt;&lt;p&gt;A key highlight of ACROSS is an intensive, multi-platform measurement campaign in the summer of 2022. It will use instruments staged on an airborne platform, a tower in the Rambouillet Forest near Paris, and other ground sites. The data collected from this campaign will be analyzed and studied to extract information about tropospheric oxidation chemistry generally, but also changes observed in the situation of mixed urban and biogenic air masses.&lt;/p&gt;&lt;p&gt;This presentation will summarize plans for the ACROSS campaign.&lt;/p&gt;

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