Ultraviolet Aerodynamic Particle Sizer Research Articles

Indoor emissions of total and fluorescent supermicron particles during HOMEChem.

Inhalation of particulate matter is associated with adverse health outcomes. The fluorescent portion of supermicron particulate matter has been used as a proxy for bioaerosols. The sources and emission rates of fluorescent particles in residential environments are not well-understood. Using an ultraviolet aerodynamic particle sizer (UVAPS), emissions of total and fluorescent supermicron particles from common human activities were investigated during the HOMEChem campaign, a test-house investigation of the chemistry of indoor environments. Human occupancy and activities, including cooking and mopping, were found to be considerable sources of indoor supermicron fluorescent particles, which enhanced the indoor particle concentrations by two orders of magnitude above baseline levels. The estimated total (fluorescent) mass emission rates for the activities tested were in the range of 4-30 (1-11) mg per person meal for cooking and 0.1-4.9 (0.05-4.7) mg/h for occupancy and mopping. Model calculations indicate that, once released, the dominant fate of coarse particles (2.5-10 micrometer in diameter) was deposition onto indoor surfaces, allowing for the possibility of subsequent resuspension and consequent exposures over durations much longer than the ventilation time scale. Indoor coarse particle deposition would also contribute to soiling of indoor surfaces.

Characteristics of biological particulate matters at urban and rural sites in the North China Plain

Depending on their concentrations, sizes, and types, particulate matters of biological origins (bioPM) significantly affect human health. However, for different air environments, they are not well characterized and can vary considerably. As an example, we investigated the bioPM differences at an urban (Beijing) site and a rural (Wangdu) site in the North China Plain (NCP) using an online monitoring instrument, an ultraviolet aerodynamic particle sizer (UV-APS), the limulus amebocyte lysate (LAL) assay, and a high-throughput sequencing method. Generally, lower concentrations of viable bioPM (hourly mean: 1.3 × 103 ± 1.6 × 103 m−3) and endotoxin (0.66 ± 0.16 EU/m3) in Beijing were observed compared to viable bioPM (0.79 × 105 ± 1.4 × 105 m−3) and endotoxin (15.1 ± 23.96 EU/m3) at the Wangdu site. The percentage of viable bioPM number concentration in the total PM was 3.1% in Beijing and 6.4% in Wangdu. Approximately 80% of viable bioPM was found to be in the range from 1 to 2.5 μm. Nevertheless, the size distribution patterns for viable bioPM at the Beijing and Wangdu sites differed and were affected by PM pollution, leading to distinct lung deposition profiles. Moreover, the distinct diurnal variations in viable bioPM on clean days were dimmed by the PM pollution at both sites. Distinct bacterial community structures were found in the air from the Beijing and Wangdu sites. The bacterial community in urban Beijing was dominated by genus Lactococcus (49.5%) and Pseudomonas (15.1%), while the rural Wangdu site was dominated by Enterococcus (65%) and Paenibacillus (10%). Human-derived genera, including Myroides, Streptococcus, Propionibacterium, Dietzia, Helcococcus, and Facklamia, were higher in Beijing, suggesting bacterial emission from humans in the urban air environment. Our results show that different air harbors different biological species, and people residing in different environments thus could have very different biological particle exposure.

Laboratory Validation and Initial Field Testing of an Unobtrusive Bioaerosol Detector for Health Care Settings

ABSTRACT Microorganisms can be transmitted from infected to healthy people as an aerosol. Military bioaerosol detectors currently used by soldiers or first responders may potentially be utilized in health care settings as part of a strategy to prevent the spread of airborne infectious diseases. The goal of this study was to conduct initial laboratory and field validation of an inexpensive and unobtrusive TACBIO detector and compare its performance with that of an expensive bioaerosol detection instrument, the Ultraviolet Aerodynamic Particle Sizer (UV-APS). The laboratory validation test used three bacterial clusters (Bacillus thuringiensis [Bt], Bacillus anthracis Sterne [BaS], and Bacillus atrophaeus var. globigii [Bg]) generated at controlled rates by an ink jet aerosol generator (IJAG). The detection efficiency of the UV-APS was ≥ 99% for all particle generation rates and species. The TACBIO detector exhibited a slightly lower detection efficiency but was still able to detect > 88% of Bt and BaS and 62.7–81.7% of Bg. Field validation conducted with simultaneous UV-APS and TACBIO sampling in an occupied hospital clinic showed both instruments closely tracking each other in detecting fluorescent particles > 1.5 µm in diameter. During a 6 hour sampling period, fluorescent particle (> 1.5 µm) concentrations showed wide short term variation connected to nearby human activity while smaller nonfluorescent particles displayed more gradual changes. These results indicate the usefulness of an unobtrusive environmental aerosol sampler in health care settings, motivating future field characterization and validation studies.

Characterization of steady-state fluorescence properties of polystyrene latex spheres using off- and online spectroscopic methods

Abstract. Fluorescent dyed polystyrene latex spheres (PSLs) are commonly used for characterization and calibration of instruments detecting fluorescence signals from particles suspended in the air and other fluids. Instruments like the Ultraviolet Aerodynamic Particle Sizer (UV-APS) and the Waveband Integrated Bioaerosol Sensor (WIBS) are widely used for bioaerosol research, but these instruments present significant technical and physical challenges requiring careful characterization with standard particles. Many other research communities use flow cytometry and other instruments that interrogate fluorescence from individual particles, and these also frequently rely on fluorescent PSLs as standards. Nevertheless, information about physical properties of commercially available PSLs provided by each manufacturer is generally proprietary and rarely available, making their use in fluorescence validation and calibration very difficult. This technical note presents an overview of steady-state fluorescence properties of fluorescent and non-fluorescent PSLs, as well as of polystyrene-divinylbenzene (PS-DVB) particles, by using on- and offline spectroscopic techniques. We show that the “fluorescence landscape” of PSLs is more complex than the information typically provided by manufacturers may imply, especially revealing multimodal emission patterns. Furthermore, non-fluorescent PSLs also exhibit defined patterns of fluorescent emission originating from a mixture of polystyrene and detergents, which becomes a crucial point for fluorescence threshold calibrations and qualitative comparison between instruments. By comparing PSLs of different sizes, but doped with the same dye, changes in emission spectra from bulk solutions are not immediately obvious. On a single-particle scale, however, fluorescence intensity values increase with increasing particle size. No significant effect in the fluorescence signatures was detectable by comparing PSLs in dry vs. wet states, indicating that solvent water may only play a minor role as a fluorescence quencher. Because information provided by manufacturers of commercially available PSLs is generally very limited, we provide the steady-state excitation–emission matrices (EEMs) of PSLs as open-access data within the Supplement. Detergent and solvent effects are also discussed in order to provide information not available elsewhere to researchers in the bioaerosol and other research communities. These data are not meant to serve as a fundamental library of PSL properties because of the variability of fluorescent properties between batches and as a function of particle aging and agglomeration. The data presented, however, provide a summary of spectral features which are consistent across these widely used fluorescent standards. Using these concepts, further checks will likely be required by individual researchers using specific lots of standards.

Fluorescent biological aerosol particles: Concentrations, emissions, and exposures in a northern California residence.

Residences represent an important site for bioaerosol exposure. We studied bioaerosol concentrations, emissions, and exposures in a single-family residence in northern California with 2 occupants using real-time instrumentation during 2 monitoring campaigns (8weeks during August-October 2016 and 5weeks during January-March 2017). Time- and size-resolved fluorescent biological aerosol particles (FBAP) and total airborne particles were measured in real time in the kitchen using an ultraviolet aerodynamic particle sizer (UVAPS). Time-resolved occupancy status, household activity data, air-change rates, and spatial distribution of size-resolved particles were also determined throughout the house. Occupant activities strongly influenced indoor FBAP levels. Indoor FBAP concentrations were an order of magnitude higher when the house was occupied than when the house was vacant. Applying an integral material-balance approach, geometric mean of total FBAP emissions from human activities observed to perturb indoor levels were in the range of 10-50million particles per event. During the summer and winter campaigns, occupants spent an average of 10 and 8.5hours per day, respectively, awake and at home. During these hours, the geometric mean daily-averaged FBAP exposure concentration (1-10μm diameter) was similar for each subject at 40particles/L for summer and 29 particles/L for winter.

Systematic characterization and fluorescence threshold strategies for the wideband integrated bioaerosol sensor (WIBS) using size-resolved biological and interfering particles

Abstract. Atmospheric particles of biological origin, also referred to as bioaerosols or primary biological aerosol particles (PBAP), are important to various human health and environmental systems. There has been a recent steep increase in the frequency of published studies utilizing commercial instrumentation based on ultraviolet laser/light-induced fluorescence (UV-LIF), such as the WIBS (wideband integrated bioaerosol sensor) or UV-APS (ultraviolet aerodynamic particle sizer), for bioaerosol detection both outdoors and in the built environment. Significant work over several decades supported the development of the general technologies, but efforts to systematically characterize the operation of new commercial sensors have remained lacking. Specifically, there have been gaps in the understanding of how different classes of biological and non-biological particles can influence the detection ability of LIF instrumentation. Here we present a systematic characterization of the WIBS-4A instrument using 69 types of aerosol materials, including a representative list of pollen, fungal spores, and bacteria as well as the most important groups of non-biological materials reported to exhibit interfering fluorescent properties. Broad separation can be seen between the biological and non-biological particles directly using the five WIBS output parameters and by taking advantage of the particle classification analysis introduced by Perring et al. (2015). We highlight the importance that particle size plays on observed fluorescence properties and thus in the Perring-style particle classification. We also discuss several particle analysis strategies, including the commonly used fluorescence threshold defined as the mean instrument background (forced trigger; FT) plus 3 standard deviations (σ) of the measurement. Changing the particle fluorescence threshold was shown to have a significant impact on fluorescence fraction and particle type classification. We conclude that raising the fluorescence threshold from FT + 3σ to FT + 9σ does little to reduce the relative fraction of biological material considered fluorescent but can significantly reduce the interference from mineral dust and other non-biological aerosols. We discuss examples of highly fluorescent interfering particles, such as brown carbon, diesel soot, and cotton fibers, and how these may impact WIBS analysis and data interpretation in various indoor and outdoor environments. The performance of the particle asymmetry factor (AF) reported by the instrument was assessed across particle types as a function of particle size, and comments on the reliability of this parameter are given. A comprehensive online supplement is provided, which includes size distributions broken down by fluorescent particle type for all 69 aerosol materials and comparing threshold strategies. Lastly, the study was designed to propose analysis strategies that may be useful to the broader community of UV-LIF instrumentation users in order to promote deeper discussions about how best to continue improving UV-LIF instrumentation and results.

Investigation of live and dead status of airborne bacteria using UVAPS with LIVE/DEAD® BacLight Kit

Although the amount of allergens and toxins being originated from viable bacteria is higher than that from dead bacteria, monitoring concentrations of dead bacteria as well as live bacteria is an important issue related to human health. The ultraviolet aerodynamic particle sizer (UVAPS) is an instrument to measure the size distribution of only viable bioaerosols. Therefore, the main objective of this study is to detect percentages of dead as well as live airborne bacteria by using a LIVE/DEAD BacLight Bacterial Viability Kit (L7012, Molecular probes, USA) together with UVAPS. Two different bacteria species, Escherichia coli (E.coli) and Micrococcus luteus (M. luteus), were used for tests. Percentages of fluorescence emitted from these bacteria were compared with those from standard PSL and dust particles. The increased percentages for dead E. coli and dead M. luteus were 41% and 75%, respectively, while this kit did not show any effective influence on fluorescence percentages of polystyrene latex and dust particles. Field test was carried out in various indoor environments to investigate percentages of live and dead airborne bacteria.

Sources and dynamics of fluorescent particles in hospitals.

Fluorescent particles can be markers of bioaerosols and are therefore relevant to nosocomial infections. To date, little research has focused on fluorescent particles in occupied indoor environments, particularly hospitals. In this study, we aimed to determine the spatial and temporal variation of fluorescent particles in two large hospitals in Brisbane, Australia (one for adults and one for children). We used an Ultraviolet Aerodynamic Particle Sizer (UVAPS) to identify fluorescent particle sources, as well as their contribution to total particle concentrations. We found that the average concentrations of both fluorescent and non-fluorescent particles were higher in the adults' hospital (0.06×106 and 1.20×106 particles/m3 , respectively) than in the children's hospital (0.03×106 and 0.33×106 particles/m3 , respectively) (P<.01). However, the proportion of fluorescent particles was higher in the children's hospital. Based on the concentration results and using activity diaries, we were able to identify sources of particle production within the two hospitals. We demonstrated that particles can be easily generated by a variety of everyday activities, which are potential sources of exposure to pathogens. Future studies to further investigate their role in nosocomial infection are warranted.

Liquid impinger BioSampler's performance for size-resolved viable bioaerosol particles

This study aimed at studying the collection efficiencies of the widely used SKC BioSampler when sampling size-resolved biological viable aerosol particles using an Ultraviolet Aerodynamic Particle Sizer (UV-APS) unit. The test bioaerosols include aerosolized bacterial species and those from indoor air. For optimal performance, different flow rates (Qsampl) (5, 12.5 and 20L/min) and different volumes of collection liquids (Vcl) (5, 10 and 20mL) were tested for bioaerosol particles from 0.5 to 10µm. In addition, the DNA stain method-the LIVE/DEAD BacLight dye and culturing were also utilized to confirm the viable bioaerosol collection efficiencies of the BioSampler.Experimental data showed that when sampling aerosolized Bacillus subtilis at the flow rate of 12.5L/min, the collection efficiency of the BioSampler decreased from 82.7% (at Vcl=20mL) to 24.8% (at Vcl=5mL). The results from the BacLight dye and culturing performed for the samples collected by the BioSampler achieved similar conclusions. When sampling indoor air particles, the overall collection efficiencies of all viable biological particles were 95.3%, 87.7% and 65.5%, respectively, for Vcl=20mL, 10mL and 5mL at the flow rate of 12.5L/min. When Qsampl was 20L/min, the BioSampler performed better with Vcl= 5mL than other volumes. The results from this work suggest that the sampling flow rate plays a dominant role in the overall physical collection efficiency while the collection volume is crucial in preserving the viability of bioaerosol particles. Different from general practice, the operating parameters for the BioSampler should thus be adjusted respectively for target viral, bacterial and fungal aerosol particles.

Fluorescent bioaerosol particle, molecular tracer, and fungal spore concentrations during dry and rainy periods in a semi-arid forest

Abstract. Bioaerosols pose risks to human health and agriculture and may influence the evolution of mixed-phase clouds and the hydrological cycle on local and regional scales. The availability and reliability of methods and data on the abundance and properties of atmospheric bioaerosols, however, are rather limited. Here we analyze and compare data from different real-time ultraviolet laser/light-induced fluorescence (UV-LIF) instruments with results from a culture-based spore sampler and offline molecular tracers for airborne fungal spores in a semi-arid forest in the southern Rocky Mountains of Colorado. Commercial UV-APS (ultraviolet aerodynamic particle sizer) and WIBS-3 (wideband integrated bioaerosol sensor, version 3) instruments with different excitation and emission wavelengths were utilized to measure fluorescent aerosol particles (FAPs) during both dry weather conditions and periods heavily influenced by rain. Seven molecular tracers of bioaerosols were quantified by analysis of total suspended particle (TSP) high-volume filter samples using a high-performance anion-exchange chromatography system with pulsed amperometric detection (HPAEC-PAD). From the same measurement campaign, Huffman et al. (2013) previously reported dramatic increases in total and fluorescent particle concentrations during and immediately after rainfall and also showed a strong relationship between the concentrations of FAPs and ice nuclei (Huffman et al., 2013; Prenni et al., 2013). Here we investigate molecular tracers and show that during rainy periods the atmospheric concentrations of arabitol (35.2 ± 10.5 ng m−3) and mannitol (44.9 ± 13.8 ng m−3) were 3–4 times higher than during dry periods. During and after rain, the correlations between FAP and tracer mass concentrations were also significantly improved. Fungal spore number concentrations on the order of 104 m−3, accounting for 2–5 % of TSP mass during dry periods and 17–23 % during rainy periods, were obtained from scaling the tracer measurements and from multiple analysis methods applied to the UV-LIF data. Endotoxin concentrations were also enhanced during rainy periods, but showed no correlation with FAP concentrations. Average mass concentrations of erythritol, levoglucosan, glucose, and (1 → 3)-β-D-glucan in TSP samples are reported separately for dry and rainy weather conditions. Overall, the results indicate that UV-LIF measurements can be used to infer fungal spore concentrations, but substantial development of instrumental and data analysis methods appears to be required for improved quantification.

Fluorescent biological aerosol particle measurements at a tropical high-altitude site in southern India during the southwest monsoon season

Abstract. An ultraviolet aerodynamic particle sizer (UV-APS) was continuously operated for the first time during two seasons to sample the contrasting winds during monsoon and winter to characterize the properties of fluorescent biological aerosol particles (FBAPs), at a high-altitude site in India. Averaged over the entire monsoon campaign (1 June–21 August 2014), the arithmetic mean number and mass concentrations of coarse-mode (&gt; 1 µm) FBAPs were 0.02 cm−3 and 0.24 µg m−3, respectively, which corresponded to ∼ 2 and 6 % of total aerosol loading, respectively. Average FBAP number size distribution exhibited a peak at ∼ 3 µm, which is attributed to the fungal spores, as supported by scanning electron microscope (SEM) images, and these results are consistent with previous studies made for FBAPs. During 11 weeks of measurements the variability of the total coarse-mode particle number (TAP) concentration was high compared to that observed in FBAP number concentrations. The TAP and FBAP number concentrations measured at this site were strongly dependent on changes in wind direction and rainfall. During periods of westerly/southwesterly winds with heavy persistent rainfall, the TAP and FBAP concentrations exhibited very low values (1.3 and 0.005 cm−3, respectively) with no significant diurnal variations, whereas during periods of northerly winds with scattered rainfall FBAPs exhibited relatively high concentration values (0.05 cm−3) with pronounced diurnal variations, which were strongly coupled with diurnal variations in meteorological parameters. The campaign-averaged FBAP number concentrations were shown to correlate with daily patterns of meteorological parameters and were positively correlated with relative humidity (RH; R2 = 0.58) and negatively with temperature (R2 = 0.60) and wind speed (R2 = 0.60). We did not observe any significant positive correlation with precipitation as reported by previous researchers from selected areas. These measurement results confirm the fact that the ratio of PBAPs to TAP is strongly dependent on particle size and location and thus may constitute a significant proportion of total aerosol particles.

Microbial aerosol characteristics in highly polluted and near-pristine environments featuring different climatic conditions

There is an increasing interest in understanding ambient bioaerosols due to their roles both in health and in climate. Here, we deployed an Ultraviolet Aerodynamic Particle Sizer to monitor viable (fluorescent) bioaerosol concentration levels at city centers (highly polluted) and their corresponding suburbs (near pristine) (total 40 locations) in 11 provinces featuring different climate zones in China between July 16 and 28, 2013. The concentration levels of viable bioaerosol particles (BioPM) of >0.5μm were measured, and corresponding percentages of BioPM% (biological fraction of total PM) and BioPM2.5% (biological fraction of PM2.5) in particulate matter (PM) and BioPM, respectively, were determined. For some key cities, indoor viable bioaerosol levels were also obtained. In addition, bacterial structures of the air samples collected across these monitoring locations were studied using pyrosequencing. BioPM concentration levels ranged from 2.1 × 104 to 2.4 × 105/m3 for city centers [BioPM% = 6.4% (±6.3%)] and 0.5 × 104 to 4.7 × 105/m3 for suburbs [BioPM% = 10% (±8.7%)]. Distinctive bioaerosol size distribution patterns were observed for different climate zones, e.g., some had fluorescence peaks at 3μm, while the majority had peaks at 1μm. Ambient bacterial aerosol community structures were also found different for different geophysical locations. Results suggest that there was a poor overall relationship between PM and BioPM across 40 monitoring locations (R2 = 0.081, two-tailed P value = 0.07435). Generally, city centers had higher PM concentrations than suburbs, but not BioPM and BioPM%. Indoor bioaerosol levels were found at least tenfold higher than those corresponding outdoors. Bacillus was observed to dominate the bacterial aerosol community in the air sample.

Bioaerosol emissions and detection of airborne antibiotic resistance genes from a wastewater treatment plant

Abstract Air samples from twelve sampling sites (including seven intra-plant sites, one upwind site and four downwind sites) from a wastewater treatment plant (WWTP) in Beijing were collected using a Reuter Centrifugal Sampler High Flow (RCS); and their microbial fractions were studied using culturing and high throughput gene sequence. In addition, the viable (fluorescent) bioaerosol concentrations for 7 intra-plant sites were also monitored for 30 min each using an ultraviolet aerodynamic particle sizer (UV-APS). Both air and water samples collected from the plant were investigated for possible bacterial antibiotic resistance genes and integrons using polymerase chain reaction (PCR) coupled with gel electrophoresis. The results showed that the air near sludge thickening basin was detected to have the highest level of culturable bacterial aerosols (up to 1697 CFU/m3) and fungal aerosols (up to 930 CFU/m3). For most sampling sites, fluorescent peaks were observed at around 3–4 μm, except the office building with a peak at 1.5 μm, with a number concentration level up to 1233–6533 Particles/m3. About 300 unique bacterial species, including human opportunistic pathogens, such as Comamonas Testosteroni and Moraxella Osloensis, were detected from the air samples collected over the biological reaction basin. In addition, we have detected the sul2 gene resistant to cotrimoxazole (also known as septra, bactrim and TMP-SMX) and class 1 integrase gene from the air samples collected from the screen room and the biological reaction basin. Overall, the screen room, sludge thickening basin and biological reaction basin imposed significant microbial exposure risks, including those from airborne antibiotic resistance genes.

Seasonal and Diurnal Variations of Fluorescent Bioaerosol Concentration and Size Distribution in the Urban Environment

A recently introduced fluorescence based real-time bioaerosol instrument, BioScout, and an ultraviolet aerodynamic particle sizer (UVAPS) were used to study fluorescent bioaerosol particles (FBAP) in the Helsinki metropolitan area, Finland, during winter and summer. Two FBAP modes at 0.5–1.5 µm (fine) and 1.5–5 µm (coarse) were detected during the summer, whereas the fine mode dominated in the winter. The concentration and proportion of the coarse FBAP was high in summer (0.028 #/cm 3 , 23%) and low in winter (0.010 #/cm 3 , 6%). Snow cover and low biological activity were assumed to be the main reasons for the low coarse FBAP concentration in the wintertime. Both the fine and the coarse FBAP fraction typically increased at nighttime during the summer. Correlations between the BioScout and the UVAPS were high with the coarse (R = 0.83) and fine (R = 0.92) FBAP. The BioScout showed 2.6 and 9.7 times higher detection efficiencies for the coarse and fine FBAP, respectively, compared to the UVAPS. A long-range transport episode of particles from Eastern Europe increased the fine FBAP concentration by over two orders of magnitude compared to the clean period in the winter, but these FBAP probably also included fluorescent non-biological particles. Correlation analysis indicates that local combustion sources did not generate fluorescent non-biological particles that can disturb fine FBAP counting. The results provide information that can be used to estimate health risks and climatic relevance of bioaerosols in the urban environment.

Effects of fungal species, cultivation time, growth substrate, and air exposure velocity on the fluorescence properties of airborne fungal spores.

Real-time bioaerosol monitoring is possible with fluorescence based instruments. This study provides information on major factors that can affect the fluorescence properties of airborne fungal spores. Two fluorescence-based bioaerosol detectors, BioScout, and ultraviolet aerodynamic particle sizer (UVAPS), were used to study fluorescent particle fractions (FPFs) of released spores of three fungal species (Aspergillus versicolor, Cladosporium cladosporioides, and Penicillium brevicompactum). Two culture media (agar and gypsum board), three ages of the culture (one week, one month, and four months), and three aerosolization air velocities (5, 15, and 27 m/s) were tested. The results showed that the FPF values for spores released from gypsum were typically lower than for those released from agar indicating that poor nutrient substrate produces spores with lower amounts of fluorescent compounds. The results also showed higher FPF values with lower air velocities in aerosolization. This indicates that easily released fully developed spores have more fluorescent compounds compared to forcibly extracted non-matured spores. The FPFs typically were lower with older samples. The FPF results between the two instruments were similar, except with four-month-old samples. The results can be utilized in field measurements of fungal spores to estimate actual concentrations and compare different instruments with fluorescence-based devices as well as in instrument calibration and testing in laboratory conditions. Fluorescence-based instruments are the only choice for real-time detection of fungal spores at the moment. In general, all fluorescence-based bioaerosol instruments are tested against known bacterial and fungal spores in laboratory conditions. This study showed that fungal species, growth substrate, age of culture, and air current exposure rate have an effect on detection efficiency of fungal spores in the fluorescence-based instruments. Therefore, these factors should be considered in the instrument calibration process. The results are also important when interpreting results of fluorescence-based field measurements of fungal spores.

Airflow resistance and bio-filtering performance of carbon nanotube filters and current facepiece respirators

This study aimed to study airflow resistance of carbon nanotube (CNT)-based filtration material and compare its bioaerosol filtering performances with commercially available facepiece respirators. Firstly, we developed a manikin-based system to evaluate the filtering performances of six respiratory masks for biological aerosol particles using an Ultraviolet Aerodynamic Particle Sizer (UV-APS). Secondly, CNT filters with a base filter with a pore size of 10μm were prepared using single-walled carbon nanotube (SWNT) loadings of 0.05, 0.1 and 0.2mg/cm2. In addition, mask filter membranes were also made by manually cutting the materials of the tested respiratory masks, and their filtration efficiencies and pressure drops were measured and compared with those of CNT-based filters.Results indicated that most of the studied respirator masks achieved a practical protection efficiency of >90%, while N95 types obtained more than 99% absolute protection efficiency under fully sealed conditions. Increasing CNT loading was shown to increase the quality factor (QF) for the CNT filter given all the sizes considered. For the loading of 0.2mg/cm2, CNT filters achieved 87% filtration efficiency against indoor viable bioaerosols and 70% for outdoor aerosol particles; and its QF was significantly higher than those of base filter, activated carbon and surgical mask filters. Different from other mask filters, CNT filters were observed to have higher biological aerosol particle filtration efficiencies than the total aerosol particles. Future work in improving air permeability of CNT filter and CNT distribution on filter support would lead to next generation respiratory mask.

Fluorescence spectra and biological activity of aerosolized bacillus spores and MS2 bacteriophage exposed to ozone at different relative humidities in a rotating drum

Biological aerosols (bioaerosols) released into the environment may undergo physical and chemical transformations when exposed to atmospheric constituents such as solar irradiation, reactive oxygenated species, ozone, free radicals, water vapor and pollutants. Aging experiments were performed in a rotating drum chamber subjecting bioaerosols, Bacillus thuringiensis Al Hakam (BtAH) spores and MS2 bacteriophages to ozone at 0 and 150ppb, and relative humidities (RH) at 10%, 50%, and 80+%. Fluorescence spectra and intensities of the aerosols as a function of time in the reaction chamber were measured with a single particle fluorescence spectrometer (SPFS) and an Ultra-Violet Aerodynamic Particle Sizer® Spectrometer (UV-APS). Losses in biological activity were measured by culture and quantitative polymerase chain reaction (q-PCR) assay. For both types of aerosols the largest change in fluorescence emission was between 280 and 400nm when excited at 263nm followed by fluorescence emission between 380 and 700nm when excited at 351nm. The fluorescence for both BtAH and MS2 were observed to decrease significantly at high ozone concentration and high RH when excited at 263nm excitation. The decreases in 263nm excited fluorescence are indicative of hydrolysis and oxidation of tryptophan in the aerosols. Fluorescence measured with the UV-APS (355-nm excitation) increased with time for both BtAH and MS2 aerosols. A two log loss of MS2 bacteriophage infectivity was observed in the presence of ozone at ~50% and 80% RH when measured by culture and normalized for physical losses by q-PCR. Viability of BtAH spores after exposure could not be measured due to the loss of genomic material during experiments, suggesting degradation of extracelluar DNA attributable to oxidation. The results of these studies indicate that the physical and biological properties of bioaerosols change significantly after exposure to ozone and water vapor.

Ambient measurements of biological aerosol particles near Killarney, Ireland: a comparison between real-time fluorescence and microscopy techniques

Abstract. Primary biological aerosol particles (PBAPs) can contribute significantly to the coarse particle burden in many environments. PBAPs can thus influence climate and precipitation systems as cloud nuclei and can spread disease to humans, animals, and plants. Measurement data and techniques for PBAPs in natural environments at high time- and size resolution are, however, sparse, and so large uncertainties remain in the role that biological particles play in the Earth system. In this study two commercial real-time fluorescence particle sensors and a Sporewatch single-stage particle impactor were operated continuously from 2 August to 2 September 2010 at a rural sampling location in Killarney National Park in southwestern Ireland. A cascade impactor was operated periodically to collect size-resolved particles during exemplary periods. Here we report the first ambient comparison of a waveband integrated bioaerosol sensor (WIBS-4) with a ultraviolet aerodynamic particle sizer (UV-APS) and also compare these real-time fluorescence techniques with results of fluorescence and optical microscopy of impacted samples. Both real-time instruments showed qualitatively similar behavior, with increased fluorescent bioparticle concentrations at night, when relative humidity was highest and temperature was lowest. The fluorescent particle number from the FL3 channel of the WIBS-4 and from the UV-APS were strongly correlated and dominated by a 3 μm mode in the particle size distribution. The WIBS FL2 channel exhibited particle modes at approx. 1 and 3 μm, and each was correlated with the concentration of fungal spores commonly observed in air samples collected at the site (ascospores, basidiospores, Ganoderma spp.). The WIBS FL1 channel exhibited variable multimodal distributions turning into a broad featureless single mode after averaging, and exhibited poor correlation with fungal spore concentrations, which may be due to the detection of bacterial and non-biological fluorescent particles. Cladosporium spp., which are among the most abundant fungal spores in many terrestrial environments, were not correlated with any of the real-time fluorescence channels, suggesting that the real-time fluorescence instruments are relatively insensitive to PBAP classes with dark, highly absorptive cell walls. Fluorescence microscopy images of cascade impactor plates showed large numbers of coarse-mode particles consistent with the morphology and weak fluorescence expected of sea salt. Some of these particles were attached to biological cells, suggesting that a marine source influenced the PBAPs observed at the site and that the ocean may be an important contributor to PBAP loadings in coastal environments.

Size‐resolved fluorescent biological aerosol particle concentrations and occupant emissions in a university classroom

This study is among the first to apply laser-induced fluorescence to characterize bioaerosols at high time and size resolution in an occupied, common-use indoor environment. Using an ultraviolet aerodynamic particle sizer, we characterized total and fluorescent biological aerosol particle (FBAP) levels (1-15 μm diameter) in a classroom, sampling with 5-min resolution continuously during eighteen occupied and eight unoccupied days distributed throughout a one-year period. A material-balance model was applied to quantify per-person FBAP emission rates as a function of particle size. Day-to-day and seasonal changes in FBAP number concentration (NF ) values in the classroom were small compared to the variability within a day that was attributable to variable levels of occupancy, occupant activities, and the operational state of the ventilation system. Occupancy conditions characteristic of lecture classes were associated with mean NF source strengths of 2 × 10(6) particles/h/person, and 9 × 10(4) particles per metabolic g CO2 . During transitions between lectures, occupant activity was more vigorous, and estimated mean, per-person NF emissions were 0.8 × 10(6) particles per transition. The observed classroom peak in FBAP size at 3-4 μm is similar to the peak in fluorescent and biological aerosols reported from several studies outdoors. Coarse particles that exhibit fluorescence at characteristic wavelengths are considered to be proxies for biological particles. Recently developed instruments permit their detection and sizing in real time. In a mechanically ventilated classroom, emissions from human occupants were a strong determinant of coarse-mode fluorescent biological aerosol particle (FBAP) levels. Human FBAP emission rates were significant under quiet occupancy conditions and increased with activity level. Fluorescent particle emissions peaked at a diameter of 3–4 μm, which is the expected modal size of airborne particles with associated microbes. Human activity patterns, and associated coarse FBAP and total particle levels varied strongly on short timescales. Thus, the dynamic temporal behavior of aerosol concentrations must be considered when determining collection protocols for samples meant to be representative of average concentrations using time-integrated or ‘snapshot’ bioaerosol measurement techniques.

Charge levels and Gram (±) fractions of environmental bacterial aerosols

Here, we investigated charge levels and Gram (+/–) fractions of environmental bacterial aerosols. The bioaerosols with +/– charges were collected separately over different time periods using an electrostatic sampler. Air samples were cultivated using selective media for G+ and G–, and further confirmed by Gram stain method. In addition, the viable bioaerosol size distributions over a 24h time period were also obtained using an ultraviolet aerodynamic particle sizer (UV-APS). Finally, the elementary charge units carried by environmental G+ and G– bacterial aerosols were derived based on distribution-weighted particle aerodynamic diameters.Results showed that G+ had equal abundances with G– regardless of the charge polarity and environments. The outdoor viable bioaerosols were observed to have slightly smaller distribution-weighted particle size (1.64µm) than that (1.79µm) of the indoor environment. In general, the outdoor culturable bacterial aerosol charge levels turned to be normally-distributed with a peak around 21–29 elementary charge units, while the indoor ones seemed to be skewed toward 46–92 elementary charge units. Results here suggest that a significant fraction of viable-but-not-culturable (VBNC) bioaerosol particles might be present for indoor environments. Results here can not only help design better electrostatic sampling device, but also assist in bioaerosol exposure assessment.