Wlodek Zahorowski

Bio: Wlodek Zahorowski is an academic researcher from Australian Nuclear Science and Technology Organisation. The author has contributed to research in topics: Radon & Air mass. The author has an hindex of 17, co-authored 27 publications receiving 912 citations.

Chemical characterization of the boundary layer outflow of air pollution to Hong Kong during February–April 2001

Abstract: [1] As a cooperative effort with the TRACE-P and ACE-Asia intensive in the spring of 2001, trace gases and aerosols were measured at a relatively remote coastal site (Hok Tsui) in southeastern Hong Kong. The main objective of the measurement program was to provide continuous ground-based data in the subtropical region of eastern Asia and to characterize the southward outflow of continental pollution that prevails in the lower atmosphere during early spring. In this paper, we present the results for ozone, CO, NO, NOy ,S O2, 222 Radon, methane and C2–C8 nonmethane hydrocarbons (NMHCs), C1–C2 halocarbons, and C1–C5 alkyl nitrate measurements obtained between 19 February and 30 April 2001. The average mixing ratios of O3, CO, SO2, and NOy were 45 ppbv, 404 ppbv, 1.8 ppbv, and 10.4 ppbv, respectively. The two dominant NMHCs were ethane (mean: 2368 pptv) and ethyne (mean: 1402 pptv), followed by propane (814 pptv), toluene (540 pptv), benzene (492 pptv), ethene (498 pptv), and n-butane (326 pptv). The most abundant halocarbon was CH3Cl (mean: 821 pptv), while 2-BuONO2 and i-PrONO2 were the two dominant alkyl nitrates species with a mean mixing ratio of 20 pptv and 19 pptv, respectively. The levels of trace gases were strongly influenced by the outflow of continental air masses initiated by the passage of cold fronts. The data are segregated into four air mass groups according to the levels of 222 Rn and wind direction, representing fresh continental outflow, coastal, perturbed maritime, and local urban air. Ozone and CO showed a moderate positive correlation (r 2 = 0.4) in the marine air group, characterized by low 222 Rn and CO levels, but they were poorly correlated in the other air mass groups. SO2 and NOy exhibited good correlations (r 2 > 0.6) with each other but were poorly correlated with CO, indicating differences in their emission sources and/or removal processes. CO very strongly correlated with ethyne and benzene (r 2 > 0.85) and also showed good correlations with several other NMHCs. Moreover, CO correlated moderately with a biomass burning tracer (CH3Cl) and an urban/industrial tracer (C2Cl4) indicating the impact of mixed pollution from urban and biomass burning sources. The relationship of CO, SO2, and NOy with the indicator of atmospheric processing, ethyne/ CO and propane/ethane, were also examined. The 2001 data were compared to the results obtained in the same period in 1994 during PEM-West B. The mean ozone level in the spring of 2001 was much higher than during PEM-West B. SO2 also had higher concentrations during TRACE-P, while CO and NOy were comparable during the two campaigns. The observed difference has been discussed in the context of emission changes and variations in meteorology. Although it is difficult to draw definitive conclusions about the extent of the influence of these two factors, it appears that clearer skies and drier conditions may have been responsible for the higher ozone concentrations during the TRACE-P period. INDEX TERMS: 0345 Atmospheric Composition and Structure: Pollution—urban and regional (0305); 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry;

A map of radon flux at the Australian land surface

Abstract: . A time-dependent map of radon-222 flux density at the Australian land surface has been constructed with a spatial resolution of 0.05° and temporal resolution of one month. Radon flux density was calculated from a simple model utilising data from national gamma-ray aerial surveys; modelled soil moisture, available from 1900 in near real-time; and maps of soil properties. The model was calibrated against a data set of accumulation chamber measurements, thereby constraining it with experimental data. A notable application of the map is in atmospheric mixing and transport studies which use radon as a tracer, where it is a clear improvement on the common assumption of uniform radon flux density.

Separating remote fetch and local mixing influences on vertical radon measurements in the lower atmosphere

Abstract: Two-point radon gradients provide a direct, unambiguous measure of near-surface atmospheric mixing. A 31-month data set of hourly radon measurements at 2 and 50 m is used to characterize the seasonality and diurnal variability of radon concentrations and gradients at a site near Sydney. Vertical differencing allows separation of remote (fetch-related) effects on measured radon concentrations from those due to diurnal variations in the strength and extent of vertical mixing. Diurnal composites, grouped according to the maximum nocturnal radon gradient ( ΔC max ), reveal strong connections between radon, wind, temperature and mixing depth on subdiurnal timescales. Comparison of the bulk Richardson Number ( Ri B ) and the turbulence kinetic energy (TKE) with the radon-derived bulk diffusivity ( K B ) helps to elucidate the relationship between thermal stability, turbulence intensity and the resultant mixing. On nights with large ΔC max , K B and TKE levels are low and Ri B is well above the ‘critical’ value. Conversely, when ΔC max is small, K B and TKE levels are high and Ri B is near zero. For intermediate ΔC max , however, Ri B remains small whereas TKE and K B both indicate significantly reduced mixing. The relationship between stability and turbulence is therefore non-linear, with even mildly stable conditions being sufficient to suppress mixing. DOI: 10.1111/j.1600-0889.2011.00565.x

The Vertical Distribution of Radon in Clear and Cloudy Daytime Terrestrial Boundary Layers

Abstract: Radon (222Rn) is a powerful natural tracer of mixing and exchange processes in the atmospheric boundary layer. The authors present and discuss the main features of a unique dataset of 50 high-resolution vertical radon profiles up to 3500 m above ground level, obtained in clear and cloudy daytime terrestrial boundary layers over an inland rural site in Australia using an instrumented motorized research glider. It is demonstrated that boundary layer radon profiles frequently exhibit a complex layered structure as a result of mixing and exchange processes of varying strengths and extents working in clear and cloudy conditions within the context of the diurnal cycle and the synoptic meteorology. Normalized aircraft radon measurements are presented, revealing the characteristic structure and variability of three major classes of daytime boundary layer: 1) dry convective boundary layers, 2) mixed layers topped with residual layers, and 3) convective boundary layers topped with coupled nonprecipitating ...

An inventory of gaseous and primary aerosol emissions in Asia in the year 2000 : NASA global tropospheric experiment transport and chemical evolution over the pacific (TRACE-P): Measurements and analysis (TRACEP1)

Abstract: [i] An inventory of air pollutant emissions in Asia in the year 2000 is developed to support atmospheric modeling and analysis of observations taken during the TRACE-P experiment funded by the National Aeronautics and Space Administration (NASA) and the ACE-Asia experiment funded by the National Science Foundation (NSF) and the National Oceanic and Atmospheric Administration (NOAA). Emissions are estimated for all major anthropogenic sources, including biomass burning, in 64 regions of Asia. We estimate total Asian emissions as follows: 34.3 Tg SO 2 , 26.8 Tg NO x , 9870 Tg CO 2 , 279 Tg CO, 107 Tg CH 4 , 52.2 Tg NMVOC, 2.54 Tg black carbon (BC), 10.4 Tg organic carbon (OC), and 27.5 Tg NH 3 . In addition, NMVOC are speciated into 19 subcategories according to functional groups and reactivity. Thus we are able to identify the major source regions and types for many of the significant gaseous and particle emissions that influence pollutant concentrations in the vicinity of the TRACE-P and ACE-Asia field measurements. Emissions in China dominate the signature of pollutant concentrations in this region, so special emphasis has been placed on the development of emission estimates for China. China's emissions are determined to be as follows: 20.4 Tg SO 2 , 11.4 Tg NO x , 3820 Tg CO 2 , 116 Tg CO, 38.4 Tg CH 4 , 17.4 Tg NMVOC, 1.05 Tg BC, 3.4 Tg OC, and 13.6 Tg NH 3 . Emissions are gridded at a variety of spatial resolutions from 1° × 1° to 30 s x 30 s, using the exact locations of large point sources and surrogate GIS distributions of urban and rural population, road networks, landcover, ship lanes, etc. The gridded emission estimates have been used as inputs to atmospheric simulation models and have proven to be generally robust in comparison with field observations, though there is reason to think that emissions of CO and possibly BC may be underestimated. Monthly emission estimates for China are developed for each species to aid TRACE-P and ACE-Asia data interpretation. During the observation period of March/ April, emissions are roughly at their average values (one twelfth of annual). Uncertainties in the emission estimates, measured as 95% confidence intervals, range from a low of ±16% for SO 2 to a high of ±450% for OC.

An overview of ACE-Asia: Strategies for quantifying the relationships between Asian aerosols and their climatic impacts

Abstract: [1] The International Global Atmospheric Chemistry Program (IGAC) has conducted a series of Aerosol Characterization Experiments (ACE) that integrate in situ measurements, satellite observations, and models to reduce the uncertainty in calculations of the climate forcing due to aerosol particles. ACE-Asia, the fourth in this series of experiments, consisted of two focused components: (1) An intensive field study that sought to quantify the spatial and vertical distribution of aerosol concentrations and properties, the processes controlling their formation, evolution, and fate, and the column-integrated radiative effect of the aerosol (late March through May 2001). (2) A longer-term network of ground stations that used in situ and column-integrated measurements to quantify the chemical, physical, and optical properties of aerosols in the ACE-Asia study area and to assess their spatial and temporal (seasonal and interannual) variability (2000–2003). The approach of the ACE-Asia science team was to make simultaneous measurements of aerosol chemical, physical, and optical properties and their radiative impacts in a variety of air masses, often coordinated with satellite overpasses. Three aircraft, two research ships, a network of lidars, and many surface sites gathered data on Asian aerosols. Chemical transport models (CTMs) were integrated into the program from the start, being used in a forecast mode during the intensive observation period to identify promising areas for airborne and ship observations and then later as tools for integrating observations. The testing and improvement of a wide range of aerosol models (including microphysical, radiative transfer, CTM, and global climate models) was one important way in which we assessed our understanding of the properties and controlling processes of Asian aerosols. We describe here the scientific goals and objectives of the ACE-Asia experiment, its observational strategies, the types of observations made by the mobile platforms and stationary sites, the models that will integrate our understanding of the climatic effect of aerosol particles, and the types of data that have been generated. Eight scientific questions focus the discussion. The intensive observations took place during a season of unusually heavy dust, so we have a large suite of observations of dust and its interaction with air pollutants. Further information about ACE-Asia can be found on the project Web site at http://saga.pmel.noaa.gov/aceasia/.

Transport and Chemical Evolution over the Pacific (TRACE-P) aircraft mission: Design, execution, and first results

Abstract: The NASA Transport and Chemical Evolution over the Pacific (TRACE-P) aircraft mission was conducted in February-April 2001 over the NW Pacific (1) to characterize the Asian chemical outflow and relate it quantitatively to its sources and (2) to determine its chemical evolution. It used two aircraft, a DC-8 and a P-3B, operating out of Hong Kong and Yokota Air Force Base (near Tokyo), with secondary sites in Hawaii, Wake Island, Guam, Okinawa, and Midway. The aircraft carried instrumentation for measurements of long-lived greenhouse gases, ozone and its precursors, aerosols and their precursors, related species, and chemical tracers. Five chemical transport models (CTMs) were used for chemical forecasting. Customized bottom-up emission inventories for East Asia were generated prior to the mission to support chemical forecasting and to serve as a priori for evaluation with the aircraft data. Validation flights were conducted for the Measurements Of Pollution In The Troposphere (MOPITT) satellite instrument and revealed little bias (6 plus or minus 2%) in the MOPITT measurements of CO columns. A major event of transpacific Asian pollution was characterized through combined analysis of TRACE-P and MOPITT data. The TRACE-P observations showed that cold fronts sweeping across East Asia and the associated warm conveyor belts (WCBs) are the dominant pathway for Asian outflow to the Pacific in spring. The WCBs lift both anthropogenic and biomass burning (SE Asia) effluents to the free troposphere, resulting in complex chemical signatures. The TRACE-P data are in general consistent with a priori emission inventories, lending confidence in our ability to quantify Asian emissions from socioeconomic data and emission factors. However, the residential combustion source in rural China was found to be much larger than the a priori, and there were also unexplained chemical enhancements (HCN, CH3Cl, OCS, alkylnitrates) in Chinese urban plumes. The Asian source of CCl4 was found to be much higher than government estimates. Measurements of HCN and CH3CN indicated a dominant biomass burning source and ocean sink for both gases. Large fractions of sulfate and nitrate were found to be present in dust aerosols. Photochemical activity in the Asian outflow was strongly reduced by aerosol attenuation of UV radiation, with major implications for the concentrations of HOx, radicals. New particle formation, apparently from ternary nucleation involving NH3, was observed in Chinese urban plumes.