Measured Air Concentrations Research Articles

Ambient air concentrations of plant protection products: Data collection for the combined air concentration database and associated risk assessment

CropLife Europe collected literature values from monitoring studies measuring air concentrations of Plant Protection Products (PPPs) that may be inhaled by humans located in rural areas but not immediately adjacent to PPP applications. The resulting “Combined Air Concentration Database” (CACD) was used to determine whether air concentrations of PPPs reported by the French “Agency for Food, Environmental and Occupational Health & Safety” (ANSES) are consistent with those measured by others to increase confidence in values of exposure to humans. The results were put into risk assessment context. Results show that 25–90% of samples do not contain measurable PPP concentrations. Measured respirable fractions were below EU default air concentrations used for risk assessment for resident exposure by the European Food Safety Authority. All measured exposures in the CACD were also below established toxicological endpoints, even when considering the highest maximum average reported concentrations and very conservative inhalation rates. The highest recorded air concentration was for prosulfocarb (0.696 μg/m³ measured over 48 h) which is below the EFSA default limit of 1 μg/m³ for low volatility substances. In conclusion, based on the CACD, measured air concentrations of PPPs are significantly lower than EFSA default limits and relevant toxicological reference values.

The influence of displacement ventilation on indoor carbon dioxide exposure and ventilation efficiency in a living laboratory open-plan office

Good indoor air quality in office environments is essential for occupant health and productivity. In open-plan offices, displacement ventilation has been recognized for its higher efficiency compared to mixing ventilation. This study evaluates the performance of displacement ventilation in an open-plan office under cooling and heating conditions, considering various supply ventilation rates, supply air temperatures, and occupancy levels. Field measurements were conducted over three months in a living laboratory office in a high-performance building. The indoor environment was controlled by an independent variable air volume (VAV) air conditioning system. The supply ventilation rate ranged from 6 to 12 h−1. Real-time measurements of carbon dioxide (CO2) concentrations in the supply air, return air, and breathing zone of the office were conducted to assess occupants’ exposure to CO2 and ventilation efficiency. The results show that the supply ventilation rate plays an important role in shaping the air distribution and overall effectiveness of the mechanical ventilation system. Higher supply ventilation rates can enhance air distribution robustness, improving ventilation efficiency and reducing CO2 exposure under both cooling and heating conditions. These findings also suggest the need for an optimized control logic that differs from the conventional control logic used in VAV systems. Specifically, during the heating condition of displacement ventilation, it is recommended to maintain the supply ventilation rate at a higher level to effectively mitigate the impact of occupant behavior on air quality, minimize CO2 exposure risks, and ensure a more robust and reliable indoor air distribution.

Atmospheric dispersion of radioactive materials for radiological risk assessment in case of hypothetical sodium cooled fast reactor accident

The latest advancements in nuclear power, namely the Generation IV (Gen IV) reactor design, have been successfully chosen in numerous countries. These cutting-edge reactor designs boast superior safety and increased fuel efficiency compared to their predecessors. Among the Gen IV designs is the sodium-cooled fast breeder reactor, and to substantiate the safety assertions, HYSPLIT (Hybrid Single-Particle Lagrangian Integrated Trajectory) dispersion modeling evolved by the National Oceanic and Atmospheric Administration (NOAA) will be employed to scrutinize the potential consequences of an accident. In this context, the analysis focuses on the 1250 MWt/500 MWe sodium-cooled fast breeder reactor (SFR) and its partial fuel melt accident, considering the crucial radioactive reduction factor. Despite existing studies on the consequences of SFR accidents, these studies need to pay more attention to the significance of the radiation reduction factor. This factor is paramount in accurately calculating dose outcomes, as not all radioactive materials can disperse freely within structures, thereby reducing inhalation and cloud shine doses. Furthermore, this investigation underscores the impact of meteorological data and dispersion model input parameters, such as release heights of radioactive materials and measured air concentration heights, on the results of atmospheric dispersion models. Hence, uncertainties in dispersion models arise due to the variability in these factors. The HYSPLIT dispersion model estimates a cumulative dose of 1.65 rem (0.0165 Sv) for a partial fuel melt scenario. The research reveals a maximum dose of approximately 1.8 rem (0.018 Sv) within a 24-hour period, indicating compliance with NRC limitations for Indian fast reactor accident consequences.

The Puy de Dôme ICe Nucleation Intercomparison Campaign (PICNIC): comparison between online and offline methods in ambient air

Abstract. Ice crystal formation in mixed-phase clouds is initiated by specific aerosol particles, termed ice-nucleating particles (INPs). Only a tiny fraction of all aerosol particles are INPs, providing a challenge for contemporary INP measurement techniques. Models have shown that the presence of INPs in clouds can impact their radiative properties and induce precipitation formation. However, for a qualified implementation of INPs in models, measurement techniques able to accurately detect the temperature-dependent INP concentration are needed. Here we present measurements of INP concentrations in ambient air under conditions relevant to mixed-phase clouds from a total of 10 INP methods over 2 weeks in October 2018 at the Puy de Dôme observatory in central France. A special focus in this intercomparison campaign was placed on having overlapping sampling periods. Although a variety of different measurement principles were used, the majority of the data show INP concentrations within a factor of 5 of one another, demonstrating the suitability of the instruments to derive model-relevant INP data. Lower values of comparability are likely due to instrument-specific features such as aerosol lamina spreading in continuous-flow diffusion chambers, demonstrating the need to account for such phenomena when interpreting INP concentration data from online instruments. Moreover, consistently higher INP concentrations were observed from aerosol filters collected on the rooftop at the Puy de Dôme station without the use of an aerosol inlet.

Modeling of PM concentrations on a construction site based on IoT monitoring system

An IoT-based system framework integrating a distributed sensor network was implemented to collect real-time data at a construction site. Various sensors were utilized to gather data concerning particulate matter (PM2.5 and PM10 concentrations) as well as meteorological parameters - wind speed, humidity, pressure, and temperature. The real-time measurements results provide an overview of air pollution levels at the construction site, revealing its association with earth excavation work, the primary construction activity. This connection allows for better management aimed at reducing concentrations of suspended particles. Through on-site monitoring of two pollutant concentrations, this study identified that the dust levels resulting from excavation activities were relatively high. It can be concluded that earth excavation significantly impacts air quality in the construction area. While exploring the primary factors influencing construction dust concentrations, the correlations indicate that these concentrations were not significantly associated with meteorological factors. To predict PM2.5 and PM10 concentrations in the air using number of working machines and meteorological parameters as predictors, both Multiple linear regression (MLR) and Artificial Neural Network (ANN) models were applied. The ANN model demonstrates better alignment with the measured air concentrations compared to the MLR model. The ANN model demonstrated an R-squared value of 0.674 for PM10 and 0.618 for PM2.5, indicating a strong predictive capability. The aim of this research, through modeling PM2.5 and PM10 concentrations in the air at the construction site is to indicate importance of the topic, especially with respect to the health of the constuction site workers.

A comparison between field measurements of vapour concentrations of plant protection products and predictions by the BROWSE model

A database of field measurements of air concentrations of pesticide active ingredients has previously been compiled by CropLife Europe with an aim to revise the default air concentration values and assumptions applied in assessing vapour exposure in the risk assessment of bystanders and residents. The BROWSE model, released in 2014, which is a regulatory risk assessment model that includes the exposure of residents and bystanders has a component relating to post-application vapour inhalation. Predictions of concentration deduced from exposures obtained using the BROWSE model were compared with field measurements of 24-h and 7-day average concentrations. The methodology for obtaining concentration estimates from the BROWSE model is described, and the criteria for including field studies in the comparison are given. The field data were adjusted to account for differences between the field experiment and the BROWSE scenario using factors derived from a separate plume dispersion model. This showed that BROWSE provides a satisfactory level of conservatism in determining potential exposures of residents and bystanders to vapour and could be a reliable alternative to replace the current EFSA approach for predicting vapour inhalation exposures for pesticides where no compound-specific data are available.

Measuring low formaldehyde exposure values in the dissection hall after embalming human body donors with ethanol-based fixation methods

The dissection course plays a central role in teaching anatomy and body donors are also needed in clinical-anatomical courses. In order to reduce formaldehyde exposure of students, participants and staff during these courses, we employed fixation solutions with low formaldehyde content. In this study, we present two ethanol-based protocols, and elucidate their suitability for the dissection process and compliance with occupational exposure limits for formaldehyde and other hazardous substances. Body donors were fixed according to an ethanol- based fixation protocol for the dissection course or an ethanol-glycerin-based fixation protocol for specialist training courses. The quality of fixation was determined during the dissection process. Exposure to hazardous substances (formaldehyde, ethanol, 2-phenoxyethanol) was measured in a regular dissection course setting at different locations (room-related and person-related measurements), and exposure indices were calculated. The quality of fixation of both methods was good and fulfilled all requirements of the student dissection course and the specialist training courses, respectively. Exposure to all hazardous substances remained well below the exposure limits. Room-related air concentration measurements were 0.073/0.058 mg/m³ (2016/2017) for formaldehyde and 65/107 mg/m³ (2016/2017) for ethanol. Person-related measurements amounted to 0.107-0.229 mg/m³ for formaldehyde and 268- 388 mg/m³ for ethanol. Room-related and person- related concentrations of 2-phenoxyethanol remained below the detection limit. The ethanol-based embalming protocols presented here offer a good alternative for the different applications. The protocols are discussed regarding current regulations and further measures to reduce formaldehyde exposure.

141 Total Reactive Isocyanate Group (Trig) Measurement – a Commentary

Abstract Exposure to airborne isocyanates has, for decades, been a leading cause of occupational. As respiratory sensitisers, isocyanates can induce allergic respiratory diseases with symptoms persisting even without further exposure. As this cause of occupational asthma is recognised it should be almost entirely preventable. In several countries isocyanates are assigned occupational exposure limits based on the total of reactive isocyanate groups (TRIG). The measurement of TRIG has some significant advantages over the measurement of individual isocyanate compounds. This exposure metric is explicit, simplifying calculations and comparisons across published data. It reduces the risk of underestimating exposure by ‘missing’ important isocyanate compounds that may be present but are not the target analytes. It allows for quantification of exposure to complex mixtures of isocyanates, di-isocyanates monomers, prepolymers, polyisocyanates, oligomers, and/or intermediate forms. This is becoming increasingly important as more complex isocyanate products are being used in the workplace. There are many methods and techniques for measuring air concentrations / potential exposure to isocyanates. Several established methods have been standardised and published as International Organization for Standardization (ISO) methods. While some may be applied directly for determination of TRIG, others (developed for determination of individual isocyanates), require modification. This presentation aims to highlight the relative merits and limitations of those methods capable of determining TRIG and also considers potential future developments.

Evaluation of the seasonal variation of VOC surface emissions and indoor air concentrations in a public building with bio-based insulation

The use of bio-based insulation materials is widely spreading in buildings. Due to their organic load, they can be an important source of Volatile Organic Compounds (VOCs). This study is among the first that evaluates the spatial and seasonal in-field VOC surface emissions from bio-based and conventional building structures as a whole, in a French public building insulated with wood wool. In addition to surface emissions, measurements of VOC concentrations in indoor air were taken. Results showed that a spatial difference (up to 5 times) in VOC emissions was observed due to the inhomogeneity of the surface. Moreover, the cardinal orientation of building structures with the same constitution induced a difference (up to a factor 30) in emission rates due to the exposure to different hygrothermal conditions. The variation in temperature and relative humidity between seasons led to higher summer VOC emissions and indoor air concentrations. In addition, indoor VOC concentrations were shown to be higher at night compared to daytime due to the decreased ventilation rate. Furthermore, an interesting approach was developed in this study to have a primary overview of the impact of surface emissions on indoor VOC levels. Results confirmed that the three bio-based walls have no significant specific VOC emissions at high rates compared to the floor and the ceiling. Bio-based insulations showed no impact on microbial indoor air concentrations during the two seasons. Moreover, no detected VOCs could be attributed to microbial development as they were also emitted from building materials.

Atmospheric deposition of reactive nitrogen to a deciduous forest in the southern Appalachian Mountains.

Assessing nutrient critical load exceedances requires complete and accurate atmospheric deposition budgets for reactive nitrogen (Nr). The exceedance is the total amount of Nr deposited to the ecosystem in excess of the critical load, which is the amount of Nr input below which harmful effects do not occur. Total deposition includes all forms of Nr (i.e., organic and inorganic) deposited to the ecosystem by wet and dry pathways. Here we present results from the Southern Appalachian Nitrogen Deposition Study (SANDS), in which a combination of measurements and field-scale modeling was used to develop a complete annual Nr deposition budget for a deciduous forest at the Coweeta Hydrologic Laboratory. Wet deposition of ammonium, nitrate, nitrite, and bulk organic N were measured directly. The dry deposited Nr fraction was estimated using a bidirectional resistance-based model driven with speciated measurements of Nr air concentrations (e.g., ammonia, ammonium aerosol, nitric acid, nitrate aerosol, bulk organic N in aerosol, total alkyl nitrates, and total peroxy nitrates), micrometeorology, canopy structure, and biogeochemistry. Total annual deposition was ~6.7 kg N ha-1 yr-1, which is on the upper end of Nr critical load estimates recently developed for similar ecosystems in the nearby Great Smoky Mountains National Park. Of the total (wet + dry) budget, 51.1% was contributed by reduced forms of Nr , with oxidized and organic forms contributing ~41.3% and 7.6%, respectively. Our results indicate that reductions in deposition would be needed to achieve the lowest estimates (~3.0 kg N ha-1 yr-1) of Nr critical loads in southern Appalachian forests.

Bayesian transdimensional inverse reconstruction of the Fukushima Daiichi caesium 137 release

Abstract. The accident at the Fukushima Daiichi nuclear power plant (NPP) yielded massive and rapidly varying atmospheric radionuclide releases. The assessment of these releases and of the corresponding uncertainties can be performed using inverse modelling methods that combine an atmospheric transport model with a set of observations and have proven to be very effective for this type of problem. In the case of the Fukushima Daiichi NPP, a Bayesian inversion is particularly suitable because it allows errors to be modelled rigorously and a large number of observations of different natures to be assimilated at the same time. More specifically, one of the major sources of uncertainty in the source assessment of the Fukushima Daiichi NPP releases stems from the temporal representation of the source. To obtain a well-time-resolved estimate, we implement a sampling algorithm within a Bayesian framework – the reversible-jump Markov chain Monte Carlo – in order to retrieve the distributions of the magnitude of the Fukushima Daiichi NPP caesium 137 (137Cs) source as well as its temporal discretization. In addition, we develop Bayesian methods that allow us to combine air concentration and deposition measurements as well as to assess the spatio-temporal information of the air concentration observations in the definition of the observation error matrix. These methods are applied to the reconstruction of the posterior distributions of the magnitude and temporal evolution of the 137Cs release. They yield a source estimate between 11 and 24 March as well as an assessment of the uncertainties associated with the observations, the model, and the source estimate. The total reconstructed release activity is estimated to be between 10 and 20 PBq, although it increases when the deposition measurements are taken into account. Finally, the variable discretization of the source term yields an almost hourly profile over certain intervals of high temporal variability, signalling identifiable portions of the source term.

Measured air concentrations of pesticides for the estimation of exposure to vapour in European risk assessments

There is an identified need to revise the default air concentration values and assumptions applied in assessing vapour exposure in the risk assessment of bystanders and residents to plant protection products. To address this, we evaluated inhalation exposure via vapour using previously unpublished data from 29 field and wind tunnel studies. The database comprises 35 trials with 11 active ingredients covering a wide range of scenarios with respect to vapour pressure, crops, application rates and European regions. Of the 961 individual measurements, 634 were below the Limit of Detection (LOD), 282 were between the LOD and Limit of Quantification (LOQ) and only 45 (4.7%) were quantifiable. Ten individual non-normalized samples exceeded 0.1 μg/m³. Of the 81 first-day measurements after the application, 36 were <LOD, and quantifiable mean, 75th and 95th percentiles values were 0.114, 0.083, 0.552 μg/m³/kg AI applied/ha, respectively. No robust correlations between air concentration and temperature, leaf coverage, humidity, wind speed, and field size were identified; there is very limited correlation between air concentration and vapour pressure and Henry's constant in a subset of the data. These data indicate that potentially inhalable pesticide vapour within or near fields occurs only at very low concentrations in real scenarios.

Air concentrations of volatile organic compounds associated with conventional and "green" cleaning products in real-world and laboratory settings.

The use of household cleaning products can result in exposure to potentially hazardous volatile and semi-volatile organic compounds (VOCs and SVOCs). "Green" cleaning products have become increasingly available, but there is no official "green" standard, and it is difficult for consumers to know what chemicals they may be exposed to while cleaning. We measured air concentrations of 46 VOCs and SVOCs of concern released from conventional and "green" cleaning products during both real-world household cleaning and a controlled chamber environment, with a focus on chemicals that might increase women's risk of breast cancer, including possible carcinogens, reproductive/developmental toxicants, or endocrine disruptors. Air samples were analyzed using gas chromatography-mass spectrometry and high-performance liquid chromatography. First, in a study of 50 women cleaning their own homes using either conventional or "green" cleaning products, we recorded the products used and collected air samples from the breathing zone to determine whether specific products or types of products were associated with increased concentrations of specific VOCs and SVOCs. The results showed that women who used conventional bleach products, disinfecting wipes, and dish soap had higher breathing zone air concentrations of several VOCs, including chloroform, carbon tetrachloride, hexaldahyde, and 1,4-dioxane, than women who did not use these products. While fewer "green" products were associated with increases in VOC air concentrations, use of "green" all-purpose cleaners was associated with increases in air concentrations of some fragrance chemicals of concern. In the laboratory, we then selected 9 of the most common conventional products and 7 "green" products used in the in-home study for measurement of the same VOCs using a continuous stirred cylindrical flow-through chamber. We found that 75% of the highest VOC emissions were emitted by conventional cleaning products, but we also identified VOC emissions of concern from green products. VOC emissions in the chamber largely agreed with the modeled associations from real-world cleaning.

Gaseous Air Pollutants and Respirable Crystalline Silica Inside and Outside Homes at Brick Kilns in Bhaktapur, Kathmandu Valley, Nepal.

Household and ambient air pollution remain public health problems in much of the world. Brick kiln employees in Nepal may be particularly at risk of high air pollution exposures and resulting health effects due to high levels of outdoor air pollution, substandard housing, and indoor biomass cooking. We conducted a cross-sectional study of indoor and outdoor air pollution concentrations at workers’ homes at four fixed chimney Bull’s trench brick kilns in Bhaktapur, Kathmandu Valley, Nepal. We measured air concentrations of carbon monoxide (CO), carbon dioxide (CO2), nitrogen dioxide (NO2), sulfur dioxide (SO2), and respirable crystalline silica (SiO2; cristobalite, quartz, tridymite) using established methods and conducted a survey about characteristics of homes or samples that may be associated with air pollution concentrations. Geometric mean concentrations of CO, CO2, and SiO2 (quartz) were 0.84 ppm, 1447.34 ppm, and 6.22 µg/m3, respectively, whereas concentrations of all other air pollutants measured below lower detection limits. Most characteristics of homes or samples were not associated with air pollution concentrations. We found a positive association between the variable how long lived in house and SiO2 (quartz) concentrations, which may reflect sustained take-home exposure to SiO2 (quartz) over time. Interventions should focus on administrative controls to reduce take-home exposure to SiO2 (quartz) in this population.

Multipass Raman gas analyzer for monitoring of atmospheric air composition

An improved gas analyzer based on Raman spectroscopy is presented. The device can measure the content of all molecular species of atmospheric air, whose concentration exceeds the sensitivity threshold. To obtain a high signal-to-noise ratio, a multi-pass optical system for scattering excitation was used together with the compression of the analyzed gas sample to a pressure of 20 atm. A technique for deriving concentrations from Raman spectra of atmospheric air based on the contour fit method is described. At the working pressure, a good agreement between the measurements of the daily air concentration of the carbon dioxide (CO2) and methane (CH4), and the data obtained with a high-sensitive CRDS gas analyzer was obtained. The standard deviation of the measured CH4 concentration values was ∼ 20 ppb. Estimates are given for the detection limits of the most common gas impurities in air, as well as for the Raman scattering cross sections for formaldehyde (CH2O), benzene (C6H6), and toluene (C7H8) vapor.

Occupational Exposure of Hairdressers to Airborne Hazardous Chemicals: A Scoping Review.

Introduction: Exposure to hazardous chemicals released during hairdressing activities from hair care products puts hairdressers at risk of adverse health effects. Safety assessments of hair products are mainly focused on consumers, but exposure for professional hairdressers might be substantially higher. Objective: To identify and assess available research data on inhalation exposures of professional hairdressers. Methods: A systematic search of studies between 1 January 2000 and 30 April 2021 was performed in Medline, Embase, Web of Science and in Cochrane registry, toxicological dossiers of the Scientific Committee on Consumer Safety (SCCS) of the European Commission as well as the German MAK Commission. Studies reporting quantitative data on airborne concentrations of chemicals in the hairdresser’s workplace were considered. The outcome was an airborne concentration of chemicals in the working environment, which was compared, when possible, with current occupational exposure limits (OEL) or guidance levels. Results: In total, 23 studies performed in 14 countries were included. The average number of hairdressing salons per study was 22 (range 1–62). Chemicals most frequently measured were formaldehyde (n = 8), ammonia (n = 5), total volatile organic compounds (TVOC) (n = 5), and toluene (n = 4). More than fifty other chemicals were measured in one to three studies, including various aromatic and aliphatic organic solvents, hydrogen peroxide, persulfate, and particulate matter. Most studies reported environmental air concentrations, while personal exposure was measured only in seven studies. The measured air concentrations of formaldehyde, ammonia, and TVOC exceeded OEL or guidance values in some studies. There was large variability in measuring conditions and reported air concentrations differed strongly within and between studies. Conclusion: Hairdressers are exposed to a wide spectrum of hazardous chemicals, often simultaneously. Airborne concentrations of pollutants depend on salon characteristics such as ventilation and the number of customers but also on used products that are often country- or client-specific. For exposure to formaldehyde, ammonia, and TVOC exceeding OELs or guidance values for indoor air was observed. Therefore, occupational exposure should be taken into account by safety regulations for hair care products.

Assessment of worker chemical exposures in California vape shops

E-cigarettes are battery-operated devices that heat a liquid mixture to make an aerosol that is inhaled, or vaped, by the user. Vape shops are retail environments designed to fulfill customer demand for diverse e-liquid flavors and hardware options, which create unique worker exposure concerns. To characterize exposures to vape shop workers, especially to flavoring chemicals associated with known respiratory toxicity, this study recruited vape shops from the San Francisco Bay Area. In six shops, we measured air concentrations for volatile organic compounds, formaldehyde, flavoring chemicals, and nicotine in personal and/or area samples; analyzed components of e-liquids vaped during field visits; and assessed metals on surface wipe samples. Interviews and observations were conducted over the course of a workday in the same six shops and interviews were performed in an additional six where sampling was not conducted. Detections of the alpha-diketone butter flavoring chemicals diacetyl and/or 2,3-pentanedione were common: in the headspace of purchased e-liquids (18 of 26 samples), in personal air samples (5 of 16), and in area air samples (2 of 6 shops). Two exceedances of recommended exposure limits for 2,3-pentanedione (a short-term exposure limit and an 8-hr time-weighted average) were measured in personal air samples. Other compounds detected in the area and personal air samples included substitutes for diacetyl and 2,3-pentanedione (acetoin and 2,3-hexanedione) and compounds that may be contaminants or impurities. Furthermore, a large variety (82) of other flavoring chemicals were detected in area air samples. None of the 12 shops interviewed had a health and safety program. Six shops reported no use of any personal protective equipment (PPE) (e.g., gloves, chemical resistant aprons, eye protection) and the others stated occasional use; however, no PPE use was observed during any field investigation day. Recommendations were provided to shops that included making improvements to ventilation, hygiene, use of personal protective equipment, and, if possible, avoidance of products containing the alpha-diketone flavoring chemicals. Future research is needed to evaluate the long-term health risks among workers in the vape shop retail industry and for e-cigarette use generally. Specific areas include further characterizing e-liquid constituents and emissions, evaluating ingredient health risks, evaluating the contributions of different routes of exposure (dermal, inhalation, and ingestion), and determining effective exposure mitigation measures.

Reassessment of the radiocesium resuspension flux from contaminated ground surfaces in eastern Japan

Abstract. Resuspension of 137Cs from the contaminated ground surface to the atmosphere is essential for understanding the environmental behaviors of 137Cs and estimating external and inhalation exposure of residents. Kajino et al. (2016) assessed the 137Cs resuspension flux from bare soil and forest ecosystems in eastern Japan in 2013 using a numerical simulation constrained by surface air concentration measurements. However, the simulation was found to underestimate the observed deposition amounts by 2 orders of magnitude. The reason for this underestimation is that the simulation assumed that resuspended 137Cs is carried by submicron aerosols, which have low deposition rates. Based on the observational indications that soil dust and bioaerosols are the major carriers of resuspended 137Cs, a new simulation is performed with higher deposition rates constrained by both surface concentrations and deposition amounts. In the new estimation, the total areal annual resuspension of 137Cs in 2013 is 25.7 TBq, which is equivalent to 0.96 % of the initial deposition (2.68 PBq). Due to the rapid deposition rates, the annual redeposition amount is also large at 10.6 TBq, approximately 40 % of the resuspended 137Cs. The resuspension rate through the atmosphere (0.96 % yr−1) seems slow, but it (2.6 × 10−5 d−1) may not be negligibly small compared to the actual decreasing trend of the ambient gamma dose rate obtained in Fukushima Prefecture after the radioactive decay of 137Cs plus 134Cs in 2013 is subtracted (1.0–7.9 × 10−4 d−1): resuspension can account for 1 %–10 % of the decreasing rate due to decontamination and natural decay through land surface processes. The current simulation underestimated the 137Cs deposition in Fukushima city in winter by more than an order of magnitude, indicating the presence of additional resuspension sources. The site of Fukushima city is surrounded by major roads. Heavy traffic on wet and muddy roads after snow removal operations could generate superlarge (approximately 100 µm in diameter) road dust or road salt particles, which are not included in the model but might contribute to the observed 137Cs at the site.

Spatio-Temporal Modeling of Small-Scale Ultrafine Particle Variability Using Generalized Additive Models

High-resolution measurements of ultrafine particle concentrations in ambient air are needed for the study of health human effects of long-term exposure. This work, carried out in the framework of the VIEPI project (Integrated Evaluation of Indoor Particulate Exposure), aims to extend current knowledge on small-scale spatio-temporal variability of Particle Number Concentration (PNC, considered a proxy of the ultrafine particles) at a local scale domain (1 km × 1 km). PNC measurements were made in the university district of San Lorenzo in Rome using portable condensation particle counters for 7 consecutive days at 21 sites in November 2017 and June 2018. Generalized Additive Models (GAMs) were performed in the area for winter, summer and the overall period. The log-transformed two-hour PNC averages constitute the response variable, and covariates were grouped by urban morphology, land use, traffic and meteorology. Winter PNC values were about twice the summer ones. PNC recorded in the university area were significantly lower than those observed in the external routes. GAMs showed a rather satisfactory result in order to capture the spatial variability, in accordance with those of other previous studies: variances were equal to 71.1, 79.7 and 84%, respectively, for winter, summer and the overall period.

Corrections to Kusnetz method for measurements of radon progeny concentrations in air

In 1956, H.L. Kusnetz proposed a quick method for radon progeny concentration measurement in mine atmosphere using a single gross-alpha count of a membrane-filtered air. The method is still widely used today and is based on a number of impractical assumptions. An instantaneous sampling time (less than ten seconds), is one of these assumptions that ignores the build-up and decay of the progeny on the filter paper during the sampling period, which is typically in the order of a few minutes. Of special concern is the 214Bi decay during the sampling period, since 214Po's alphas are lost during the sampling time and cannot be accounted for during the counting time. In addition, the method assumes that 214Bi activity during the counting period is constant. This inaccurate assumption can result in a smaller count rate, especially when counting times are long. Hence, underestimated working levels are expected when using Kusnetz factors without correcting for the sampling and counting times. In this technical report, exact sampling and counting time corrections to the method are provided along with the updated Kusnetz factors that correspond to common equilibrium conditions to correctly estimate the Working Level in air. Additionally, time corrections to the commonly used self-absorption correction formula and the lower level of detectability (LLD) equation used for any sample measurement are given.