36 research outputs found

    Measurements and comparison of primary biological aerosol above and below a tropical forest canopy using a dual channel fluorescence spectrometer

    Get PDF
    Original article can be found at: http://www.atmos-chem-phys.net/10/issue10.html Copyright - the authors. Authors grant any third party the right to use the article freely as long as its original authors and citation details are identified. The article and any associated published material is distributed under the Creative Commons Attribution 3.0 License.Aerosol particle size distributions were measured below and above a tropical rainforest canopy in Borneo, Malaysia, in June/July 2008 using the WIBS-3: a single particle dual channel fluorescence spectrometer. Material in the size range 0.8–20 μm was characterized according to optical equivalent diameter (DP), morphology and fluorescence at 310–400 nm and 400–600 nm following excitation at 280 nm and 370 nm respectively. Particles fluorescent after both excitations are likely to be fluorescent primary biological aerosol particles (FBAP). Measured FBAP number concentration (NFBAP) at both sites exhibited clear diurnal cycles. The largest variability was observed in the understorey, where NFBAP reached a minimum of 50–100 L−1 in late morning. In mid afternoon it exhibited strong transient fluctuations as large as 4000 L−1 that were followed by sustained concentrations of 1000–2500 L−1 that reduced steadily between midnight and sunrise. Above the canopy FBAP number ranged from 50–100 L−1 during the daytime to 200–400 L−1 at night but did not exhibit the transient enhancements seen in the understorey. The strong FBAP fluctuations were attributed to the release of fungal spores below the canopy and appeared to be linked to elevated relative humidity. The mean FBAP number fraction in the size range 0.8 μm<DP<20 μm was 55% in the understorey and 28% above canopy. A size mode at 2 μm<DP<4 μm appears at both sites and is primarily FBAP, which dominated the coarse (DP≥2.5 μm) number concentration at both sites, accounting for 75% in the understorey and 57% above the canopy. In contrast, the concentration of non-fluorescent particles (NNON) at both sites was typically 200–500 L−1, the majority of which occupied a size mode at 0.8<DP<1.5 μm. Enhanced understorey NNON was observed daily in mid-afternoon and also at midday on three occasions: the former coincided with the FBAP enhancements and measured approximately 10% of their magnitude; the latter occurred independently of the NFBAP diurnal cycle and comprised particles smaller than 2 μm. Particle diameter of 3–5 μm is consistent with smaller fungal spores, though absolute identification of biological species is not possible with the UV-LIF technique. Based on the measured FBAP and non-fluorescent particle abundances and their observed recovery times following rain showers, FBAP originated beneath the canopy while the non-fluorescent material was transported from further away. It is concluded that these separate sources contributed the majority of the aerosol measured by the WIBS-3 at both sites.Peer reviewe

    Statistical characterisation of bio-aerosol background in an urban environment

    Full text link
    In this paper we statistically characterise the bio-aerosol background in an urban environment. To do this we measure concentration levels of naturally occurring microbiological material in the atmosphere over a two month period. Naturally occurring bioaerosols can be considered as noise, as they mask the presence of signals coming from biological material of interest (such as an intentionally released biological agent). Analysis of this 'biobackground' was undertaken in the 1-10 um size range and a 3-9% contribution was found to be biological in origin - values which are in good agreement with other studies reported in the literature. A model based on the physics of turbulent mixing and dispersion was developed and validated against this analysis. The Gamma distribution (the basis of our model) is shown to comply with the scaling laws of the concentration moments of our data, which enables us to universally characterise both biological and non-biological material in the atmosphere. An application of this model is proposed to build a framework for the development of novel algorithms for bio-aerosol detection and rapid characterisation.Comment: 14 Pages, 8 Figure

    The fluorescence properties of aerosol larger than 0.8 mu m in urban and tropical rainforest locations

    Get PDF
    Original article can be found at : http://www.atmos-chem-phys.net/ Copyright the Authors 2011. This work is distributed under the Creative Commons Attribution 3.0 License.UV-LIF measurements were performed on ambient aerosol in Manchester, UK (urban city centre, winter) and Borneo, Malaysia (remote, tropical) using a Wide Issue Bioaerosol Spectrometer, version 3 (WIBS3). These sites are taken to represent environments with minor and significant primary biological aerosol (PBA) influences respectively, and the urban dataset describes the fluorescent background aerosol against which PBA must be identified by researchers using LIF. The ensemble aerosol at both sites was characterised over 2-3 weeks by measuring the fluorescence intensity and optical equivalent diameter (D(P)) of single particles sized 0.8 = 1 mu m. The WIBS3 features three fluorescence channels: the emission following a 280 nm excitation is recorded at 310-400 nm (channel F1) and 400-600 nm (F2), and fluorescence excited at 350 nm is detected at 400-600 nm (F3). In Manchester the primary size mode of fluorescent and non-fluorescent material was present at 0.8-1.2 mu m, with a secondary fluorescent mode at 2-4 mu m. In Borneo non-fluorescent material peaked at 0.8-1.2 mu m and fluorescent at 3-4 mu m. Agreement between fluorescent number concentrations in each channel differed at the two sites, with F1 and F3 reporting similar concentrations in Borneo but F3 outnumbering F1 by a factor of 2-3 across the size spectrum in Manchester. The fluorescence intensity in each channel generally rose with D(P) at both sites with the exception of F1 intensity in Manchester, which peaked at D(P) = 4 mu m, causing a divergence between F1 and F3 intensity at larger D(P). This divergence and the differing fluorescent particle concentrations demonstrate the additional discrimination provided by the F1 channel in Manchester. The relationships between fluorescence intensities in different pairs of channels were also investigated as a function of D(P). Differences between these metrics were apparent at each site and provide some distinction between the two datasets. Finally, particle selection criteria based on the Borneo dataset were applied to identify a median concentration of 10 "Borneo-like" fluorescent particles per litre in Manchester.Peer reviewe

    The fluorescence properties of aerosol larger than 0.8 μm in an urban and a PBA-dominated location

    Get PDF
    Original article can be found at: www.atmospheric-chemistry-and-physics.net Copyright Copernicus Publications. Released under Creative Commons license http://creative.commons.org/licenses/by-nc-sa/3.0/Dual-wavelength Ultraviolet light-induced fluorescence (UV-LIF) measurements were performed on ambient environmental aerosol in Manchester, UK (urban city centre, winter) and Borneo, Malaysia (remote, tropical), which are taken to represent environments with negligible and significant primary biological aerosol (PBA) influences, respectively. Single-particle fluorescence intensity and optical equivalent diameter were measured with a Wide Issue Bioaerosol Sensor, version 3 (WIBS3) in the diameter range 0.8 μm≤DP≤20 μm for 2–3 weeks and filters were analysed using energy dispersive X-ray (EDX) spectroscopy, which revealed mostly non-PBA dominated particle sizes larger than 1 μm in Manchester. The WIBS3 features three fluorescence channels: Fluorescence excited at 280 nm is recorded at 310–400 nm and 400–600 nm and fluorescence excited at 370 nm is detected at 400–600 nm. In Manchester the primary size mode of fluorescent and non-fluorescent material was at 1.2 μm. In Borneo non-fluorescent material peaked at 1.2 μm and fluorescent at 3–4 μm. The fluorescence intensity at 400–600 nm generally increased with DP at both sites, as did the 310–400 nm intensity in Borneo. In Manchester the 310–400 m fluorescence decreased at DP>4 μm, suggesting this channel offers additional discrimination between fluorescent particle types. Finally, the ratio of fluorescence intensity in two pairs of channels was investigated as a function of particle diameter and this varied significantly between the two environments, demonstrating that the fluorescent aerosol in each can in principle be distinguished using a combination of fluorescence and elastic scattering measurements.Peer reviewe

    Continuous bio-aerosol monitoring in a tropical environment using a UV fluorescence and light scattering instrument

    Get PDF
    This paper describes an instrument designed to achieve the continuous monitoring of ambient bio-aerosol concentrations. The instrument is a compact, relatively low-cost, UV aerosol spectrometer that monitors and classifies the ambient aerosol by simultaneously recording from individual airborne particles both a 2×2 fluorescence excitation-emission matrix and multi-angle spatial elastic scattering data. The former can indicate the possible presence of specific biological fluorophores within the particle whilst the latter provides an assessment of particle size and shape. Taken together, these parameters can facilitate discrimination between biological and non-biological particles and potentially allow classification of biological particle types. Example measurements are given illustrating magnitude and temporal fluctuations in the biological fraction of aerosol within the Borneo tropical rain forest

    Observations of fluorescent and biological aerosol at a high-altitude site in Central France

    Get PDF
    © Author(s) 2013. This work is distributed under the Creative Commons Attribution 3.0 LicenseTotal bacteria, fungal spore and yeast counts were compared with UV Light-Induced Fluorescence (UV-LIF) measurements of ambient aerosol at the summit of the Puy de Dˆome (pdD) mountain in Central France (1465 ma.s.l), which represents a background elevated site. Bacteria, fungal spores and yeast were enumerated by epifluorescence microscopy (EFM) and found to number 2.2 to 23 L−1 and 0.8 to 2 L−1, respectively. Bacteria counts on two successive nights were an order of magnitude larger than in the intervening day. A Wide Issue Bioaerosol Spectrometer, version 3 (WIBS-3) was used to perform UV-LIF measurements on ambient aerosol sized 0.8 to 20 µm. Mean total number concentration was 270 L−1 (σ = 66 L−1) found predominantly in a size mode at 2 µm for most of the campaign. Total concentration (fluorescent + non-fluorescent aerosol) peaked at 500 L−1 with a size mode at 1 µm because of a change in air mass origin lasting around 48 h. The WIBS-3 features two excitation and fluorescence detection wavelengths corresponding to di ff erent biological molecules. The mean fluorescent particle concentration after short-wave (280 nm; Tryptophan) excitation was 12 L−1 (σ = 6 L−1), and did not vary much through the campaign. In contrast the mean concentration of particles fluorescent after long-wave (370 nm; NADH) excitation was 95 L−1(σ = 25 L−1), and a nightly rise and subsequent fall of up to 100 L−1 formed a strong diurnal cycle in the latter. The fluorescent populations exhibited size modes at 3 µm and 2 to 3 µm, respectively. A hierarchical agglomerative cluster analysis algorithm was applied to the data and used to extract di ff erent particle factors. A cluster concentration time series representative of bacteria was identified. This was found to exhibit a diurnal cycle with a maximum peak appearing during the day. Analysis of organic mass spectra recorded using an Aerosol Mass Spectrometer 25 (AMS; Aerodyne Inc.) suggests that aerosol reaching the site at night was more aged than that during the day, indicative of sampling the residual layer at night. Supplementary meteorological data and previous work also show that pdD lies in the residual layer/free troposphere at night, and this is thought to cause the observed diurnal cycles in organic-type and fluorescent aerosol particles. Based on the observed disparity between bacteria and fluorescent particle concentrations, fluorescent non-PBA is likely to be important in the WIBS-3 data and the surprisingly high fluorescent concentration in the residual layer/free troposphere raises questions about a ubiquitous background in continental air during the summer.Peer reviewe
    corecore