scholarly journals Impact of VOCs and NOx on Ozone Formation in Moscow

Atmosphere ◽  
2020 ◽  
Vol 11 (11) ◽  
pp. 1262
Author(s):  
Elena Berezina ◽  
Konstantin Moiseenko ◽  
Andrei Skorokhod ◽  
Natalia V. Pankratova ◽  
Igor Belikov ◽  
...  
Keyword(s):  
Ground Level ◽  
Ozone Production ◽  
Anthropogenic Sources ◽  
State University ◽  
High Positive Correlation ◽  
Diurnal Variability ◽  
Elevated Ozone ◽  
Observational Site ◽  
Poor Ventilation ◽  
Ozone Episodes

Volatile organic compounds (VOCs), ozone (O3), nitrogen oxides (NOx), carbon monoxide (CO), meteorological parameters, and total non-methane hydrocarbons (NMHC) were analyzed from simultaneous measurements at the MSU-IAP (Moscow State University—Institute of Atmospheric Physics) observational site in Moscow from 2011–2013. Seasonal and diurnal variability of the compounds was studied. The highest O3 concentration in Moscow was observed in the summer daytime periods in anticyclonic meteorological conditions under poor ventilation of the atmospheric boundary layer and high temperatures (up to 105 ppbv or 210 μg/m3). In contrast, NOx, CO, and benzene decreased from 8 a.m. to 5–6 p.m. local time (LT). The high positive correlation of daytime O3 with secondary VOCs affirmed an important role of photochemical O3 production in Moscow during the summers of 2011–2013. The summertime average concentrations of the biogenic VOCs isoprene and monoterpenes were observed to be 0.73 ppbv and 0.53 ppbv, respectively. The principal source of anthropogenic VOCs in Moscow was established to be local vehicle emissions. Yet, only about 5% of the observed isoprene was safely attributed to anthropogenic sources, suggesting significant contribution of biogenic sources into the total levels of ozone precursors. The non-linear O3–NOx dependence shows a decrease in ground-level O3 with an increase in NOx during the summers of 2011–2013, which is typical for the VOC-sensitive photochemical regime of O3 formation. Nevertheless, during the elevated ozone episodes in July 2011, the photochemical regime of ozone production was either transitional or NOx-sensitive. Contribution of various anthropogenic and biogenic VOCs into the measured ozone values was evaluated. The ozone-forming potential (OFP) of total VOCs was 31–67 μg/m3 on average and exceeded 100 μg/m3 in the top 10% of high ozone events, reaching 136 μg/m3. Acetaldehyde, 1.3-butadiene, and isoprene have the highest ozone production potential in Moscow compared to that of other measured VOCs.

scholarly journals Ozone production and hydrocarbon reactivity in Hong Kong, Southern China

2007 ◽  
Vol 7 (2) ◽  
pp. 557-573 ◽  
Author(s):  
J. Zhang ◽  
T. Wang ◽  
W. L. Chameides ◽  
C. Cardelino ◽  
J. Kwok ◽  
...  
Keyword(s):  
Hong Kong ◽  
Southern China ◽  
Ground Level ◽  
Ozone Production ◽  
Back Trajectories ◽  
Ground Level Ozone ◽  
Abstract Data ◽  
The Pearl River ◽  
Ozone Episodes ◽  
The Relationship

Abstract. Data obtained in Hong Kong during the Hong Kong and the Pearl River Delta (PRD) Pilot Air Monitoring Study in autumn 2002 are analyzed to unravel the relationship between ground-level ozone (O3), pollution precursors, and cross-border transport. Ten ozone episodes, during which the hourly O3 concentration exceeded 100 ppbv in 9 cases and 90 ppbv in one case, are subject to detailed analysis, including one case with hourly O3 of 203 ppbv, which is the highest concentration on record to date in Hong Kong. Combined with high-resolution back trajectories, dCO/dNOy (the ratio of enhancement of CO concentration above background to that of NOy) is used to define whether O3 is locally or regionally produced. Five out of the ten Hong Kong O3-episodes studied show a "pollution signature" that is indicative of impact from Guangdong Province. Examination of speciated volatile organic compounds (VOCs) shows that the reactivity of VOCs is dominated by anthropogenic VOCs, of which the reactive aromatics dominate, in particular xylenes and toluene. Calculations using a photochemical box model indicate that between 50–100% of the O3 increase observed in Hong Kong during the O3 episodes can be explained by photochemical generation within the Hong Kong area, provided that nitrous acid (HONO) is present at the concentrations derived from this study. An Observation-Based Model (OBM) is used to calculate the sensitivity of the O3 production to changes in the concentrations of the precursor compounds. Generally the production of O3 throughout much of the Hong Kong area is limited by VOCs, while high nitric oxide (NO) concentrations suppress O3 concentration.

scholarly journals Ozone production and hydrocarbon reactivity in Hong Kong, Southern China

2006 ◽  
Vol 6 (5) ◽  
pp. 8961-9002 ◽  
Author(s):  
J. Zhang ◽  
T. Wang ◽  
W. L. Chameides ◽  
C. Cardelino ◽  
J. Kwok ◽  
...  
Keyword(s):  
Hong Kong ◽  
Southern China ◽  
Ground Level ◽  
Ozone Production ◽  
Back Trajectories ◽  
Ground Level Ozone ◽  
Abstract Data ◽  
The Pearl River ◽  
Ozone Episodes ◽  
The Relationship

Abstract. Data obtained in Hong Kong during the Hong Kong and the Pearl River Delta (PRD) Pilot Air Monitoring Study in autumn 2002 are analyzed to unravel the relationship between ground-level ozone (O3), pollution precursors, and cross-border transport. Ten ozone episodes, during which the hourly O3 concentration exceeded 100 ppbv in 9 cases and 90 ppbv in one case, are subject to detailed analysis, including one case with hourly O3 of 203 ppbv, which is the highest concentration on record to date in Hong Kong. Combined with high-resolution back trajectories, dCO/dNOy is used to define whether O3 is locally or regionally produced. Five out of the ten Hong Kong O3-episodes studied show a ''pollution signature'' that is indicative of impact from Guangdong Province. Examination of speciated volatile organic compounds (VOCs) shows that the reactivity of VOCs is dominated by anthropogenic VOCs, of which the reactive aromatics dominate, in particular xylenes and toluene. Calculations using a photochemical box model indicate that between 50–100% of the O3 increase observed in Hong Kong during the O3 episodes can be explained by photochemical generation within the Hong Kong area, provided that nitrous acid (HONO) is present at the concentrations derived from this study. An Observation-Based Model (OBM) is used to calculate the sensitivity of the O3 production to changes in the concentrations of the precursor compounds. Generally the production of O3 throughout much of the Hong Kong area is limited by VOCs, while high nitric oxide (NO) concentrations suppress O3 concentration.

scholarly journals Aerosol Characterization during the Summer 2017 Huge Fire Event on Mount Vesuvius (Italy) by Remote Sensing and In Situ Observations

2021 ◽  
Vol 13 (10) ◽  
pp. 2001
Author(s):  
Antonella Boselli ◽  
Alessia Sannino ◽  
Mariagrazia D’Emilio ◽  
Xuan Wang ◽  
Salvatore Amoruso
Keyword(s):  
Remote Sensing ◽  
Biomass Burning ◽  
Ground Level ◽  
Large Area ◽  
Fire Event ◽  
Near Surface ◽  
Mean Values ◽  
Microphysical Properties ◽  
Observational Site ◽  
Biomass Burning Aerosol

During the summer of 2017, multiple huge fires occurred on Mount Vesuvius (Italy), dispersing a large quantity of ash in the surrounding area ensuing the burning of tens of hectares of Mediterranean scrub. The fires affected a very large area of the Vesuvius National Park and the smoke was driven by winds towards the city of Naples, causing daily peak values of particulate matter (PM) concentrations at ground level higher than the limit of the EU air quality directive. The smoke plume spreading over the area of Naples in this period was characterized by active (lidar) and passive (sun photometer) remote sensing as well as near-surface (optical particle counter) observational techniques. The measurements allowed us to follow both the PM variation at ground level and the vertical profile of fresh biomass burning aerosol as well as to analyze the optical and microphysical properties. The results evidenced the presence of a layer of fine mode aerosol with large mean values of optical depth (AOD > 0.25) and Ångstrom exponent (γ > 1.5) above the observational site. Moreover, the lidar ratio and aerosol linear depolarization obtained from the lidar observations were about 40 sr and 4%, respectively, consistent with the presence of biomass burning aerosol in the atmosphere.

scholarly journals Study of Temporal Variations of Equivalent Black Carbon in a Coastal City in Northwest Spain Using an Atmospheric Aerosol Data Management Software

2021 ◽  
Vol 11 (2) ◽  
pp. 516
Author(s):  
María Piñeiro-Iglesias ◽  
Javier Andrade-Garda ◽  
Sonia Suárez-Garaboa ◽  
Soledad Muniategui-Lorenzo ◽  
Purificación López-Mahía ◽  
...  
Keyword(s):  
Data Management ◽  
Black Carbon ◽  
Light Absorption ◽  
Atmospheric Aerosol ◽  
Urban Areas ◽  
Radiative Properties ◽  
Anthropogenic Sources ◽  
Biomass Combustion ◽  
Management Support ◽  
Diurnal Variability

Light-absorbing carbonaceous aerosols (including black carbon (BC)) pose serious health issues and play significant roles in atmospheric radiative properties. Two-year measurements (2015–2016) of aerosol light absorption, combined with measurements of sub-micrometric particles, were continuously conducted in A Coruña (northwest (NW) Spain) to determine their light absorption properties: absorption coefficients (σabs) and the absorption Ångström exponent (AAE). The mean and standard deviation of equivalent black carbon (eBC) during the period of study were 0.85 ± 0.83 µg m−3, which are lower than other values measured in urban areas of Spain and Europe. High eBC concentrations found in winter are associated with an increase in emissions from anthropogenic sources in combination with lower mixing layer heights and frequent stagnant conditions. The pronounced diurnal variability suggests a strong influence from local sources. AAE had an average value of 1.26 ± 0.22 which implies that both fossil fuel combustion and biomass burning influenced optical aerosol properties. This also highlights biomass combustion in suburban areas, where the use of wood for domestic heating is encouraged, as an important source of eBC. All data treatment was gathered using SCALA© as atmospheric aerosol data management support software program.

scholarly journals Benzene and Toluene in the surface air of North Eurasia from TROICA-12 campaign along the Trans-Siberian railway

2016 ◽  
Author(s):  
Andrey I. Skorokhod ◽  
Elena V. Berezina ◽  
Konstantin B. Moiseenko ◽  
Nikolai F. Elansky ◽  
Igor B. Belikov
Keyword(s):  
Motor Vehicle ◽  
Regional Scale ◽  
Proton Transfer Reaction ◽  
Urban Atmosphere ◽  
Ozone Production ◽  
Anthropogenic Sources ◽  
Total Contribution ◽  
South Siberia ◽  
Ozone Photochemistry ◽  
Anthropogenic Pollutant

Abstract. Volatile organic compounds (VOCs) were measured by proton transfer reaction – mass spectrometry (PTR-MS) on a mobile laboratory in a transcontinental TROICA-12 (21.07.2008–04.08.2008) campaign along the Trans-Siberian railway from Moscow to Vladivostok. Surface concentrations of benzene (C6H6) and toluene (C7H8) along with non-methane hydrocarbons (NMHCs), CO, O3, SO2, NO, NO2 and meteorology are analyzed in this study to identify the main sources of benzene and toluene along the Trans-Siberian railway. The most measurements in the TROICA-12 campaign were conducted under low-wind/stagnant conditions in moderately (~ 78 % of measurements) to weakly polluted (~ 20 % of measurements) air directly affected by regional anthropogenic sources adjacent to the railroad. Only 2 % of measurements were identified as characteristic of highly polluted urban atmosphere. Maximum values of benzene and toluene during the campaign reached 36.5 ppb and 45.6 ppb, correspondingly, which is significantly less than their one-time maximum permissible concentrations (94 and 159 ppb for benzene and toluene, correspondingly). About 90 % of benzene and 65 % of toluene content is attributed to motor vehicle transport and 10 % and 20 %, correspondingly, provided by the other local and regional-scale sources. The highest average concentrations of benzene and toluene are measured in the industrial regions of the European Russia (up to 0.3 and 0.4 ppb for benzene and toluene, correspondingly) and south Siberia (up to 0.2 and 0.4 ppb for benzene and toluene, correspondingly). Total contribution of benzene and toluene to photochemical ozone production along the Trans-Siberian railway is about 16 % compared to the most abundant biogenic VOC – isoprene. This contribution, however, is found to be substantially higher (up to 60–70 %) in urbanized areas along the railroad suggesting important role of anthropogenic pollutant sources in regional ozone photochemistry and air quality.

scholarly journals Measurement of Ozone Production Sensor

2010 ◽  
Vol 3 (3) ◽  
pp. 545-555 ◽  
Author(s):  
M. Cazorla ◽  
W. H. Brune
Keyword(s):  
Production Rate ◽  
High Efficiency ◽  
Ambient Air ◽  
Ozone Production ◽  
State University ◽  
Photostationary State ◽  
Sample Chamber ◽  
Efficiency Conversion ◽  
The Difference ◽  
Teflon Film

Abstract. A new ambient air monitor, the Measurement of Ozone Production Sensor (MOPS), measures directly the rate of ozone production in the atmosphere. The sensor consists of two 11.3 L environmental chambers made of UV-transmitting Teflon film, a unit to convert NO2 to O3, and a modified ozone monitor. In the sample chamber, flowing ambient air is exposed to the sunlight so that ozone is produced just as it is in the atmosphere. In the second chamber, called the reference chamber, a UV-blocking film over the Teflon film prevents ozone formation but allows other processes to occur as they do in the sample chamber. The air flows that exit the two chambers are sampled by an ozone monitor operating in differential mode so that the difference between the two ozone signals, divided by the exposure time in the chambers, gives the ozone production rate. High-efficiency conversion of NO2 to O3 prior to detection in the ozone monitor accounts for differences in the NOx photostationary state that can occur in the two chambers. The MOPS measures the ozone production rate, but with the addition of NO to the sampled air flow, the MOPS can be used to study the sensitivity of ozone production to NO. Preliminary studies with the MOPS on the campus of the Pennsylvania State University show the potential of this new technique.

scholarly journals Current and future occurrences of health-relevant, compound heat and ozone pollution events in six European ozone-temperature regions 

2021 ◽  
Author(s):  
Sally Jahn ◽  
Elke Hertig
Keyword(s):  
Climate Change ◽  
Air Temperature ◽  
Large Scale ◽  
Coupled Model ◽  
Ground Level ◽  
Future Climate Change ◽  
Ozone Pollution ◽  
Ground Level Ozone ◽  
Ozone Concentrations ◽  
Elevated Ozone

<p>Air pollution and heat events present two major health risks, both already independently posing a significant threat to human health and life. High levels of ground-level ozone (O<sub>3</sub>) and air temperature often coincide due to the underlying physical relationships between both variables. The most severe health outcome is in general associated with the co-occurrence of both hazards (e.g. Hertig et al. 2020), since concurrent elevated levels of temperature and ozone concentrations represent a twofold exposure and can lead to a risk beyond the sum of the individual effects. Consequently, in the current contribution, a compound approach considering both hazards simultaneously as so-called ozone-temperature (o-t-)events is chosen by jointly analyzing elevated ground-level ozone concentrations and air temperature levels in Europe.</p><p>Previous studies already point to the fact that the relationship of underlying synoptic and meteorological drivers with one or both of these health stressors as well as the correlation between both variables vary with the location of sites and seasons (e.g. Otero et al. 2016; Jahn, Hertig 2020). Therefore, a hierarchical clustering analysis is applied to objectively divide the study domain in regions of homogeneous, similar ground-level ozone and temperature characteristics (o-t-regions). Statistical models to assess the synoptic and large-scale meteorological mechanisms which represent main drivers of concurrent o-t-events are developed for each identified o-t-region.</p><p>Compound elevated ozone concentration and air temperature events are expected to become more frequent due to climate change in many parts of Europe (e.g. Jahn, Hertig 2020; Hertig 2020). Statistical projections of potential frequency shifts of compound o-t-events until the end of the twenty-first century are assessed using the output of Earth System Models (ESMs) from the sixth phase of the Coupled Model Intercomparison Project (CMIP6).</p><p><em>Hertig, E. (2020) Health-relevant ground-level ozone and temperature events under future climate change using the example of Bavaria, Southern Germany. Air Qual. Atmos. Health. doi: 10.1007/s11869-020-00811-z</em></p><p><em>Hertig, E., Russo, A., Trigo, R. (2020) Heat and ozone pollution waves in Central and South Europe- characteristics, weather types, and association with mortality. Atmosphere. doi: 10.3390/atmos11121271</em></p><p><em>Jahn, S., Hertig, E. (2020) Modeling and projecting health‐relevant combined ozone and temperature events in present and future Central European climate. Air Qual. Atmos. Health. doi: 10.1007/s11869‐020‐009610</em></p><p><em>Otero N., Sillmann J., Schnell J.L., Rust H.W., Butler T. (2016) Synoptic and meteorological drivers of extreme ozone concentrations over Europe. Environ Res Lett. doi: 10.1088/ 1748-9326/11/2/024005</em></p>

scholarly journals The magnitude of the snow-sourced reactive nitrogen flux to the boundary layer in the Uintah Basin, Utah, USA

2016 ◽  
Vol 16 (21) ◽  
pp. 13837-13851 ◽  
Author(s):  
Maria Zatko ◽  
Joseph Erbland ◽  
Joel Savarino ◽  
Lei Geng ◽  
Lauren Easley ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Optical Properties ◽  
Oil And Gas ◽  
Nitrogen Isotopes ◽  
Ground Level ◽  
Anthropogenic Sources ◽  
Reactive Nitrogen ◽  
Actinic Flux ◽  
Nitrogen Fluxes ◽  
Uintah Basin

Abstract. Reactive nitrogen (Nr  =  NO, NO2, HONO) and volatile organic carbon emissions from oil and gas extraction activities play a major role in wintertime ground-level ozone exceedance events of up to 140 ppb in the Uintah Basin in eastern Utah. Such events occur only when the ground is snow covered, due to the impacts of snow on the stability and depth of the boundary layer and ultraviolet actinic flux at the surface. Recycling of reactive nitrogen from the photolysis of snow nitrate has been observed in polar and mid-latitude snow, but snow-sourced reactive nitrogen fluxes in mid-latitude regions have not yet been quantified in the field. Here we present vertical profiles of snow nitrate concentration and nitrogen isotopes (δ15N) collected during the Uintah Basin Winter Ozone Study 2014 (UBWOS 2014), along with observations of insoluble light-absorbing impurities, radiation equivalent mean ice grain radii, and snow density that determine snow optical properties. We use the snow optical properties and nitrate concentrations to calculate ultraviolet actinic flux in snow and the production of Nr from the photolysis of snow nitrate. The observed δ15N(NO3−) is used to constrain modeled fractional loss of snow nitrate in a snow chemistry column model, and thus the source of Nr to the overlying boundary layer. Snow-surface δ15N(NO3−) measurements range from −5 to 10 ‰ and suggest that the local nitrate burden in the Uintah Basin is dominated by primary emissions from anthropogenic sources, except during fresh snowfall events, where remote NOx sources from beyond the basin are dominant. Modeled daily averaged snow-sourced Nr fluxes range from 5.6 to 71  ×  107 molec cm−2 s−1 over the course of the field campaign, with a maximum noontime value of 3.1  ×  109 molec cm−2 s−1. The top-down emission estimate of primary, anthropogenic NOx in Uintah and Duchesne counties is at least 300 times higher than the estimated snow NOx emissions presented in this study. Our results suggest that snow-sourced reactive nitrogen fluxes are minor contributors to the Nr boundary layer budget in the highly polluted Uintah Basin boundary layer during winter 2014.

scholarly journals The impacts of precursor reduction and meteorology on ground-level ozone in the Greater Toronto Area

2014 ◽  
Vol 14 (15) ◽  
pp. 8197-8207 ◽  
Author(s):  
S. C. Pugliese ◽  
J. G. Murphy ◽  
J. A. Geddes ◽  
J. M. Wang
Keyword(s):  
Health Hazard ◽  
Ground Level ◽  
Ozone Production ◽  
Ground Level Ozone ◽  
Ozone Concentrations ◽  
Greater Toronto Area ◽  
High Solar Radiation ◽  
Linear Effects ◽  
Human Health Hazard ◽  
Ozone Levels

Abstract. Tropospheric ozone (O3) is a major component of photochemical smog and is a known human health hazard, as well as a damaging factor for vegetation. Its precursor compounds, nitrogen oxides (NOx) and volatile organic compounds (VOCs), have a variety of anthropogenic and biogenic sources and exhibit non-linear effects on ozone production. As an update to previous studies on ground-level ozone in the Greater Toronto Area (GTA), we present an analysis of NO2, VOC and O3 data from federal and provincial governmental monitoring sites in the GTA from 2000 to 2012. We show that, over the study period, summertime 24 h VOC reactivity and NO2 midday (11:00–15:00) concentrations at all sites decreased significantly; since 2000, all sites experienced a decrease in NO2 of 28–62% and in measured VOC reactivity of at least 53–71%. Comparing 2002–2003 to 2011–2012, the summed reactivity of OH towards NO2 and a suite of measured VOCs decreased from 8.6 to 4.6 s−1. Ratios of reactive VOC pairs indicate that the effective OH concentration experienced by primary pollutants in the GTA has increased significantly over the study period. Despite the continuous decrease in precursor levels, ozone concentrations are not following the same pattern at all stations; it was found that the Canada-wide Standard for ozone continues to be exceeded at all monitoring stations. Additionally, while the years 2008–2011 had consistently lower ozone levels than previous years, 2012 experienced one of the highest recorded summertime ozone concentrations and a large number of smog episodes. We demonstrate that these high ozone observations in 2012 may be a result of the number of days with high solar radiation, the number of stagnant periods and the transport of high ozone levels from upwind regions.

scholarly journals Spatiotemporal variability of NO<sub>2</sub> and PM<sub>2.5</sub> over Eastern China: observational and model analyses with a novel statistical method

2018 ◽  
Vol 18 (17) ◽  
pp. 12933-12952 ◽  
Author(s):  
Mengyao Liu ◽  
Jintai Lin ◽  
Yuchen Wang ◽  
Yang Sun ◽  
Bo Zheng ◽  
...  
Keyword(s):  
Spatial Scales ◽  
Eastern China ◽  
Ground Level ◽  
Vertical Gradient ◽  
Spatiotemporal Variability ◽  
Model Errors ◽  
Diurnal Variability ◽  
Near Surface ◽  
Synchronous Mode ◽  
The North

Abstract. Eastern China (27–41∘ N, 110–123∘ E) is heavily polluted by nitrogen dioxide (NO2), particulate matter with aerodynamic diameter below 2.5 µm (PM2.5), and other air pollutants. These pollutants vary on a variety of temporal and spatial scales, with many temporal scales that are nonperiodic and nonstationary, challenging proper quantitative characterization and visualization. This study uses a newly compiled EOF–EEMD analysis visualization package to evaluate the spatiotemporal variability of ground-level NO2, PM2.5, and their associations with meteorological processes over Eastern China in fall–winter 2013. Applying the package to observed hourly pollutant data reveals a primary spatial pattern representing Eastern China synchronous variation in time, which is dominated by diurnal variability with a much weaker day-to-day signal. A secondary spatial mode, representing north–south opposing changes in time with no constant period, is characterized by wind-related dilution or a buildup of pollutants from one day to another. We further evaluate simulations of nested GEOS-Chem v9-02 and WRF/CMAQ v5.0.1 in capturing the spatiotemporal variability of pollutants. GEOS-Chem underestimates NO2 by about 17 µg m−3 and PM2.5 by 35 µg m−3 on average over fall–winter 2013. It reproduces the diurnal variability for both pollutants. For the day-to-day variation, GEOS-Chem reproduces the observed north–south contrasting mode for both pollutants but not the Eastern China synchronous mode (especially for NO2). The model errors are due to a first model layer too thick (about 130 m) to capture the near-surface vertical gradient, deficiencies in the nighttime nitrogen chemistry in the first layer, and missing secondary organic aerosols and anthropogenic dust. CMAQ overestimates the diurnal cycle of pollutants due to too-weak boundary layer mixing, especially in the nighttime, and overestimates NO2 by about 30 µg m−3 and PM2.5 by 60 µg m−3. For the day-to-day variability, CMAQ reproduces the observed Eastern China synchronous mode but not the north–south opposing mode of NO2. Both models capture the day-to-day variability of PM2.5 better than that of NO2. These results shed light on model improvement. The EOF–EEMD package is freely available for noncommercial uses.

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