Fluorescent Particle Concentrations Research Articles

Phenanthrene release-migration characteristics and potential influencing mechanisms from paddy soil to overlying water under bioturbation in a rice-fish coculture agroecosystem

Currently, polycyclic aromatic hydrocarbons (PAHs) such as phenanthrene (Phe) in rice-fish (RF) coculture paddy fields in Northeast China pose widespread environmental pollution risks. This study constructed experimental microcosm systems to explore the release-migration rules and reveal the potential influencing mechanisms of Phe from paddy soil to overlying water under bioturbation in an RF coculture agroecosystem in this area. (1). The release of particulate Phe (P-Phe) and dissolved Phe (D-Phe) was significantly promoted by bioturbation (p<0.05). The results of Pearson correlation analysis revealed strong correlations between P-Phe and total suspended solids (TSS), D-Phe and dissolved organic carbon (DOC) (p<0.05). (2). The adsorption process of Phe at the paddy soil-overlying water interface conformed to the competitive adsorption-solubilization (CAS) model of large-molecule biological dissolved organic matter (Bio-DOM) at low concentrations (7 mg/L) (L-CBio-DOM-LM-CAS) and the coadsorption and accumulation model of small-molecule Bio-DOM at high concentrations (45 mg/L) (H-CBio-DOM-SM-CAA). (3). Ultraviolet fluorescence (UV-FS) tracing technology and reaction diffusion modeling were used to qualitatively and quantitatively simulate the migration pathway of Phe-containing paddy soil particles. The maximum fluorescent particle (f-ps) concentration of Phe migration in paddy soil was 8.23%, and the maximum bioturbation diffusion coefficient (Db) was 23.6 × 10−3 cm2/d. Bioturbation significantly altered the physicochemical properties of paddy soil (p<0.05). The results of principal component analysis (PCA) showed that particle size (<0.05 mm) is the key factor causing the Phe maximum migration concentration to be 68.39 ng/g in paddy soil. This study will provide an important research basis for the prevention and control of secondary release and migration of pollutants under bioturbation in RF coculture agroecosystems.

Subcellular detection of PEBCA particles in macrophages: combining darkfield microscopy, confocal Raman microscopy, and ToF–SIMS analysis

The detection of biomedical organic nanocarriers in cells and tissues is still an experimental challenge. Here we developed an imaging strategy for the label-free detection of poly (ethylbutyl cyanoacrylate) (PEBCA) particles. Experiments were carried out with phagocytic NR8383 macrophages exposed to non-toxic and non-activating concentrations of fluorescent (PEBCA NR668 and PEBCA NR668/IR), non-fluorescent (PEBCA), and cabazitaxel-loaded PEBCA particles (PEBCA CBZ). Exposure to PEBCA NR668 revealed an inhomogeneous particle uptake similar to what was obtained with the free modified Nile Red dye (NR668). In order to successfully identify the PEBCA-loaded cells under label-free conditions, we developed an imaging strategy based on enhanced darkfield microscopy (DFM), followed by confocal Raman microscopy (CRM) and time-of-flight secondary ion mass spectrometry (ToF–SIMS). Nitrile groups of the PEBCA matrix and PEBCA ions were used as suitable analytes for CRM and ToF–SIMS, respectively. Masses found with ToF–SIMS were further confirmed by Orbitrap-SIMS. The combined approach allowed to image small (< 1 µm) PEBCA-containing phagolysosomes, which were identified as PEBCA-containing compartments in NR8383 cells by electron microscopy. The combination of DFM, CRM, and ToF–SIMS is a promising strategy for the label-free detection of PEBCA particles.Graphical

Drivers of the fungal spore bioaerosol budget: observational analysis and global modeling

Abstract. Bioaerosols are produced by biological processes and directly emitted into the atmosphere, where they contribute to ice nucleation and the formation of precipitation. Previous studies have suggested that fungal spores constitute a substantial portion of the atmospheric bioaerosol budget. However, our understanding of what controls the emission and burden of fungal spores on the global scale is limited. Here, we use a previously unexplored source of fungal spore count data from the American Academy of Allergy, Asthma, and Immunology (AAAAI) to gain insight into the drivers of their emissions. First, we derive emissions from observed concentrations at 66 stations by applying the boundary layer equilibrium assumption. We estimate an annual mean emission of 62 ± 31 m−2 s−1 across the USA. Based on these pseudo-observed emissions, we derive two models for fungal spore emissions at seasonal scales: a statistical model, which links fungal spore emissions to meteorological variables that show similar seasonal cycles (2 m specific humidity, leaf area index and friction velocity), and a population model, which describes the growth of fungi and the emission of their spores as a biological process that is driven by temperature and biomass density. Both models show better skill at reproducing the seasonal cycle in fungal spore emissions at the AAAAI stations than the model previously developed by Heald and Spracklen (2009) (referred to as HS09). We implement all three emissions models in the chemical transport model GEOS-Chem to evaluate global emissions and burden of fungal spore bioaerosol. We estimate annual global emissions of 3.7 and 3.4 Tg yr−1 for the statistical model and the population model, respectively, which is about an order of magnitude lower than the HS09 model. The global burden of the statistical and the population model is similarly an order of magnitude lower than that of the HS09 model. A comparison with independent datasets shows that the new models reproduce the seasonal cycle of fluorescent biological aerosol particle (FBAP) concentrations at two locations in Europe somewhat better than the HS09 model, although a quantitative comparison is hindered by the ambiguity in interpreting measurements of fluorescent particles. Observed vertical profiles of FBAP show that the convective transport of spores over source regions is captured well by GEOS-Chem, irrespective of which emission scheme is used. However, over the North Atlantic, far from significant spore sources, the model does not reproduce the vertical profiles. This points to the need for further exploration of the transport, cloud processing and wet removal of spores. In addition, more long-term observational datasets are needed to assess whether drivers of seasonal fungal spore emissions are similar across continents and biomes.

Exposure route affects the distribution and toxicity of polystyrene nanoplastics in zebrafish

The widespread use of polystyrene (PS) products in a myriad of consumer products has resulted in widespread contamination of PS nanoplastics (PSNPs) in aquatic ecosystems. Fish early life stages are exposed to nanoplastics dermally and via gills. Additional routes of exposure include oral via the ingestion of contaminated prey and maternal transfer. However, there is limited amount of work studying the impact of exposure route in the toxicokinetics and toxicodynamics of PSNPs. The objective of this study was to compare the effects of exposure routes (aqueous and microinjection) on the organ distribution and toxicity of PSNPs. We “mimicked” the maternal exposure of PSNPs to zebrafish by injecting a known concentration of fluorescent particles directly into 2-cell stage embryos. Endpoints were collected starting at 96 h post-fertilization until several weeks post-hatch to evaluate depuration. Although both exposure routes led to the accumulation of PSNPs in the yolk sac followed by brain, eyes, gut and swim bladder, the aqueous exposure caused higher PSNP concentrations in the brain and eyes and the injection exposure caused PSNP accumulation mainly in the trunk area. A waterborne exposure also reduced antioxidant gene expression; increased frequency of developmental abnormalities such as bent tails, jaw deformities and pericardial edema; and resulted in lower growth rates and hypoactivity. Overall, a waterborne exposure to PSNPs resulted in higher transfer to the brain and caused greater toxic effects to zebrafish compared to an injection exposure and highlights the key role of exposure routes in the uptake, localization and subsequent distribution of nanoparticles.

Intercomparison of Multiple UV-LIF Spectrometers Using the Aerosol Challenge Simulator

Measurements of primary biological aerosol particles (PBAPs) have been conducted worldwide using ultraviolet light-induced fluorescence (UV-LIF) spectrometers. However, how these instruments detect and respond to known biological and non-biological particles, and how they compare, remains uncertain due to limited laboratory intercomparisons. Using the Defence Science and Technology Laboratory, Aerosol Challenge Simulator (ACS), controlled concentrations of biological and non-biological aerosol particles, singly or as mixtures, were produced for testing and intercomparison of multiple versions of the Wideband Integrated Bioaerosol Spectrometer (WIBS) and Multiparameter Bioaerosol Spectrometer (MBS). Although the results suggest some challenges in discriminating biological particle types across different versions of the same UV-LIF instrument, a difference in fluorescence intensity between the non-biological and biological samples could be identified for most instruments. While lower concentrations of fluorescent particles were detected by the MBS, the MBS demonstrates the potential to discriminate between pollen and other biological particles. This study presents the first published technical summary and use of the ACS for instrument intercomparisons. Within this work a clear overview of the data pre-processing is also presented, and documentation of instrument version/model numbers is suggested to assess potential instrument variations between different versions of the same instrument. Further laboratory studies sampling different particle types are suggested before use in quantifying impact on ambient classification.

Assessing the passage of particles through polyamide reverse osmosis membranes

The safety of recycled water for potable water reuse can be enhanced by improving the removal of pathogenic microorganisms through reverse osmosis (RO) membrane. The present study aimed to identify the causes of the passage of particles through intact RO membrane elements using stable 0.5 µm fluorescent (FL) microspheres as bacteria-sized surrogates. Pilot-scale tests revealed that the removal of FL particles varied between 1.6 and 6.1-log among seven commercial RO membrane modules, and a less permeable RO membrane had a higher efficiency for removing bacteria-sized particles. To clarify the causes of particles passing through the tight RO membrane, further investigations were performed focusing on the following three types of membranes based on the RO membrane manufacturing process: an ultrafiltration membrane (the supporting layer of RO membrane), and RO membranes obtained before assembly and after disassembly of their membrane elements. The highest concentrations of FL particles in permeate were obtained in the disassembled RO membranes, suggesting that the commercial spiral wound membrane elements may have lesser integrity than the intact RO membrane sheets for removal of bacteria-sized particles. However, the conductivity removal of the two types of RO membranes was equivalent regardless of the assembly process; thus, typical performance tests could not identify the membrane integrity breach for particle removal. To the best of our knowledge, this is the first study to report that the integrity of the RO membrane for particle removal may be compromised after assembling its spiral wound membrane element.

Abundance and Diurnal Trends of Fluorescent Bioaerosols in the Troposphere over Mt. Tai, China, in Spring

AbstractPrimary biological aerosol particles are ubiquitous in the global atmosphere and can affect cloud formation, deteriorate air quality, and cause human infections. Mt. Tai (1,534 m a.s.l.) is an elevated site in the North China Plain where atmospheric aerosols reflect both regional advection and long‐range transport. In this study, we deployed a Wideband Integrated Bioaerosol Sensor (WIBS‐4A) and collected total suspended particles and eight‐stage size‐segregated aerosol samples at the summit of Mt. Tai in spring from 21 March to 8 April 2017 to quantify the abundance, size distributions, and diurnal variations of fluorescent bioaerosols and to investigate the effect of different fluorescence thresholds of WIBS for ambient bioaerosol recognition. During the whole sampling period, the number concentration of fluorescent particles (&gt;0.8 μm) was 647 ± 533 L−1, accounting for 26.9% ± 10.0% by number of the total particles in that size range. Three‐dimensional excitation‐emission matrix fluorescence of water‐soluble organic matter in size‐segregated aerosols shows that humic‐like substances (HULIS) are mainly in the fine mode (&lt;2.1 μm) while protein‐like substances are mainly in the coarse mode (&gt;2.1 μm). From the diurnal variation, it is shown that bioaerosols can undergo transformation during long‐range transport and contribute to HULIS. For bioaerosol recognition, we find that 6σ‐threshold can lead to better classification of fluorescent aerosol particles for fungal spores. Overall, our results constrain the abundance of primary bioaerosols in the troposphere over East Asia and elucidate the processes for their evolution via mountain/valley breezes and long‐range transport.

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.

Analysis of Correlation between Atmospheric Fluorescent Particles and Biomaterials

Bio-aerosols are important components of atmospheric aerosols, which can affect human health depending on the origin of biological particles. A real-time monitoring technology for bio-aerosols can rapidly provide information on the current state of biological particles in ambient environment, which substantially minimize the impact of hazardous biological particles. The aim of this study is to evaluate LIF (laser-induced fluorescence) technology on real-time monitoring of bio-aerosols by investigating the correlation between biomaterial concentration (cultured microbes or extracted DNA) and fluorescent particle concentration in ambient environment. For this, we used LIF instrument, BDS (Bio-aerosol Detection System), and analyzed the correlation coefficients from the collected data (the non-fluorescent particle concentration, the fluorescent particle concentration, the cultured microbial concentration, the extracted DNA concentration). Pearson’s correlation coefficients (r) from this study are as follows: 0.85 (p<0.001) between the fluorescent particle concentration and the cultured microbial concentration, 0.93 (p< 0.001) between the fluorescent particle concentration and the extracted DNA concentration, while 0.42 (p<0.01) between the non-fluorescent particle concentration and the cultured microbial concentration, 0.49 (p<0.01) between the non-fluorescent particle concentration and the extracted DNA concentration. It was also found that the size range of the fluorescent particles, which exhibited the highest coefficient for the extracted DNA concentration and the cultured microbial concentration, was 2 to less than 10 micrometer (μm), and their coefficients were 0.89 (p<0.01) and 0.8 (p<0.001), respectively. These results indicate that the fluorescent particles, especially in the range of 2 to less than 10 μm, are highly correlated with bio-aerosols rather than the non-fluorescent particles. Taken together, LIF technology is great for real-time monitoring of bio-aerosols by counting fluorescent particles and resolving particle sizes at ambient atmospheric environment.

Driving and sorting of the fluorescent droplets on digital microfluidic platform

In this paper, we present a digital microfluidic droplet sorting platform to achieve automated droplet sorting based on fluorescent detection. We design and fabricate a kind of digital microfluidic chip for manipulating nano-liter-sized liquid droplets, and the chip is integrated with a fluorescence-initiated feedback system for real-time sorting control. The driving and sorting characteristics of fluorescent droplets encapsulating fluorescent-labeled particles are studied on this platform. The droplets dispensed from on-chip reservoir electrode are transported to a fluorescence detection site and sorted according to their fluorescence signals. The fluorescent droplets and non-fluorescent droplets are successfully separated and the number of fluorescent particles inside each droplet is quantified by its fluorescent intensity. We realize droplet sorting at 20 Hz and obtain a linear relationship between the fluorescent particle concentrations and the fluorescence signals. This work is easily adapted for sorting out fluorescent-labeled microparticles, cells and bacteria and thus has the potential of quantifying catalytic or regulatory bio-activities.

Scoping studies to establish the capability and utility of a real-time bioaerosol sensor to characterise emissions from environmental sources

A novel dual excitation wavelength based bioaerosol sensor with multiple fluorescence bands called Spectral Intensity Bioaerosol Sensor (SIBS) has been assessed across five contrasting outdoor environments. The mean concentrations of total and fluorescent particles across the sites were highly variable being the highest at the agricultural farm (2.6 cm−3 and 0.48 cm−3, respectively) and the composting site (2.32 cm−3 and 0.46 cm−3, respectively) and the lowest at the dairy farm (1.03 cm−3 and 0.24 cm−3, respectively) and the sewage treatment works (1.03 cm−3 and 0.25 cm−3, respectively). In contrast, the number-weighted fluorescent fraction was lowest at the agricultural site (0.18) in comparison to the other sites indicating high variability in nature and magnitude of emissions from environmental sources. The fluorescence emissions data demonstrated that the spectra at different sites were multimodal with intensity differences largely at wavelengths located in secondary emission peaks for λex 280 and λex 370. This finding suggests differences in the molecular composition of emissions at these sites which can help to identify distinct fluorescence signature of different environmental sources. Overall this study demonstrated that SIBS provides additional spectral information compared to existing instruments and capability to resolve spectrally integrated signals from relevant biological fluorophores could improve selectivity and thus enhance discrimination and classification strategies for real-time characterisation of bioaerosols from environmental sources. However, detailed lab-based measurements in conjunction with real-world studies and improved numerical methods are required to optimise and validate these highly resolved spectral signatures with respect to the diverse atmospherically relevant biological fluorophores.

Review: The Use of Real-Time Fluorescence Instrumentation to Monitor Ambient Primary Biological Aerosol Particles (PBAP)

Primary biological aerosol particles (PBAP) encompass many particle types that are derived from several biological kingdoms. These aerosol particles can be composed of both whole living units such as pollen, bacteria, and fungi, as well as from mechanically formed particles, such as plant debris. They constitute a significant proportion of the overall atmospheric particle load and have been linked with adverse health issues and climatic effects on the environment. Traditional methods for their analysis have focused on the direct capture of PBAP before subsequent laboratory analysis. These analysis types have generally relied on direct optical microscopy or incubation on agar plates, followed by time-consuming microbiological investigation. In an effort to address some of these deficits, real-time fluorescence monitors have come to prominence in the analysis of PBAP. These instruments offer significant advantages over traditional methods, including the measurement of concentrations, as well as the potential to simultaneously identify individual analyte particles in real-time. Due to the automated nature of these measurements, large data sets can be collected and analyzed with relative ease. This review seeks to highlight and discuss the extensive literature pertaining to the most commonly used commercially available real-time fluorescence monitors (WIBS, UV-APS and BioScout). It discusses the instruments operating principles, their limitations and advantages, and the various environments in which they have been deployed. The review provides a detailed examination of the ambient fluorescent aerosol particle concentration profiles that are obtained by these studies, along with the various strategies adopted by researchers to analyze the substantial data sets the instruments generate. Finally, a brief reflection is presented on the role that future instrumentation may provide in revolutionizing this area of atmospheric research.

Variations in airborne bacterial communities at high altitudes over the Noto Peninsula (Japan) in response to Asian dust events

Abstract. Aerosol particles, including airborne microorganisms, are transported through the free troposphere from the Asian continental area to the downwind area in East Asia and can influence climate changes, ecosystem dynamics, and human health. However, the variations present in airborne bacterial communities in the free troposphere over downwind areas are poorly understood, and there are few studies that provide an in-depth examination of the effects of long-range transport of aerosols (natural and anthropogenic particles) on bacterial variations. In this study, the vertical distributions of airborne bacterial communities at high altitudes were investigated and the bacterial variations were compared between dust events and non-dust events.Aerosols were collected at three altitudes from ground level to the free troposphere (upper level: 3000 or 2500 m; middle level: 1200 or 500 m; and low level: 10 m) during Asian dust events and non-dust events over the Noto Peninsula, Japan, where westerly winds carry aerosols from the Asian continental areas. During Asian dust events, air masses at high altitudes were transported from the Asian continental area by westerly winds, and laser imaging detection and ranging (lidar) data indicated high concentrations of non-spherical particles, suggesting that dust-sand particles were transported from the central desert regions of Asia. The air samples collected during the dust events contained 10–100 times higher concentrations of microscopic fluorescent particles and optical particle counter (OPC) measured particles than in non-dust events. The air masses of non-dust events contained lower amounts of dust-sand particles. Additionally, some air samples showed relatively high levels of black carbon, which were likely transported from the Asian continental coasts. Moreover, during the dust events, microbial particles at altitudes of &gt; 1200 m increased to the concentrations ranging from 1. 2 × 106 to 6. 6 × 106 particles m−3. In contrast, when dust events disappeared, the microbial particles at &gt; 1200 m decreased slightly to microbial-particle concentrations ranging from 6. 4 × 104 to 8. 9 × 105 particles m−3.High-throughput sequencing technology targeting 16S rRNA genes (16S rDNA) revealed that the bacterial communities collected at high altitudes (from 500 to 3000 m) during dust events exhibited higher diversities and were predominantly composed of natural-sand/terrestrial bacteria, such as Bacillus members. During non-dust periods, airborne bacteria at high altitudes were mainly composed of anthropogenic/terrestrial bacteria (Actinobacteria), marine bacteria (Cyanobacteria and Alphaproteobacteria), and plant-associated bacteria (Gammaproteobacteria), which shifted in composition in correspondence with the origins of the air masses and the meteorological conditions. The airborne bacterial structures at high altitudes suggested remarkable changes in response to air mass sources, which contributed to the increases in community richness and to the domination of a few bacterial taxa.

A simple and inexpensive technique for assessing contamination during drilling operations

AbstractSubsurface exploration relies on drilling. Normally drilling requires a drilling fluid that will infiltrate into the drill core. Drilling fluid contains non‐indigenous materials and microbes from the surface, so its presence renders a sample unsuitable for microbiological and many other analyses. Because infiltration cannot be avoided, it is of paramount importance to assess the degree of contamination to identify uncontaminated samples for geomicrobiological investigations. To do this, usually a tracer is mixed into the drilling fluid. In past drilling operations a variety of tracers have been used, each has specific strengths and weaknesses. For microspheres the main problem was the high price, which limited their use to spot checks or drilling operations that require only small amounts of drilling fluid. Here, we present a modified microsphere tracer approach that uses an aqueous fluorescent pigment dispersion with a similar concentration of fluorescent particles as previously used microsphere tracers. However, it costs four orders of magnitude less, allowing for a more liberal use even in large operations. Its applicability for deep drilling campaigns was successfully tested during two drilling campaigns of the International Continental Drilling Program (ICDP) at Lake Towuti, Sulawesi, Indonesia, and Lake Chalco, Mexico. Quantification of the tracer requires only a fluorescence microscope or a flow cytometer. The latter allowing for high‐resolution data to be obtained directly on‐site within minutes and with minimal effort, decreasing sample processing times substantially relative to traditional tracer methods. This approach offers an inexpensive, rapid, but powerful alternative technique for contamination assessment during drilling campaigns.

Fluorescent Bioaerosol Particles Resulting from Human Occupancy with and Without Respirators

Airborne transmission of pathogenic aerosols via human breath plays a major role in infectious disease outbreaks in indoor environments. Yet, their bioaerosol emission profiles are still not well quantified. Here, we first studied bioaerosol emission rates of human exhaled breath from 12 healthy subjects, and then evaluated the bioaerosol emissions when wearing two different respirators “Doctor masks” and N95 in a controlled environment (27 m3) using a bioaerosol sensor-ultraviolet aerodynamic particle spectrometer (UV-APS). The human bioaerosol contribution was further confirmed through classroom observation. The results showed that there was a peak around 1.5 µm for the fluorescent particles emitted from humans’ breath. For the controlled environment, the presence of 5 people without wearing masks increased bioaerosol concentration by 107% within 30 min at an average emission rate of 8.4 × 105 fluorescent particles person–1 hour–1 resulting from the occupancy. When wearing N95 masks or “Doctor masks”, bioaerosol increases were observed to be 81% or 31% for the controlled environment, respectively, lower compared to those without masks. In-classroom observation also showed a fluorescent particle concentration increase of about 50%. In all experiments, we observed a decline in PM number concentration. Bioaerosol emission from exhaled breath was calculated to account for about 17% of the increase in the controlled environment. The results here suggest the need for re-evaluating microbial aerosol exposure risks for medical sites that demand high levels of hygiene even while wearing a respirator.

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.

Ice nucleating particles in the Saharan Air Layer

Abstract. This study aims at quantifying the ice nucleation properties of desert dust in the Saharan Air Layer (SAL), the warm, dry and dust-laden layer that expands from North Africa to the Americas. By measuring close to the dust's emission source, before aging processes during the transatlantic advection potentially modify the dust properties, the study fills a gap between in situ measurements of dust ice nucleating particles (INPs) far away from the Sahara and laboratory studies of ground-collected soil. Two months of online INP concentration measurements are presented, which were part of the two CALIMA campaigns at the Izaña observatory in Tenerife, Spain (2373 m a.s.l.), in the summers of 2013 and 2014. INP concentrations were measured in the deposition and condensation mode at temperatures between 233 and 253 K with the Portable Ice Nucleation Chamber (PINC). Additional aerosol information such as bulk chemical composition, concentration of fluorescent biological particles as well as the particle size distribution was used to investigate observed variations in the INP concentration. The concentration of INPs was found to range between 0.2 std L−1 in the deposition mode and up to 2500 std L−1 in the condensation mode at 240 K. It correlates well with the abundance of aluminum, iron, magnesium and manganese (R: 0.43–0.67) and less with that of calcium, sodium or carbonate. These observations are consistent with earlier results from laboratory studies which showed a higher ice nucleation efficiency of certain feldspar and clay minerals compared to other types of mineral dust. We find that an increase of ammonium sulfate, linked to anthropogenic emissions in upwind distant anthropogenic sources, mixed with the desert dust has a small positive effect on the condensation mode INP per dust mass ratio but no effect on the deposition mode INP. Furthermore, the relative abundance of biological particles was found to be significantly higher in INPs compared to the ambient aerosol. Overall, this suggests that atmospheric aging processes in the SAL can lead to an increase in ice nucleation ability of mineral dust from the Sahara. INP concentrations predicted with two common parameterization schemes, which were derived mostly from atmospheric measurements far away from the Sahara but influenced by Asian and Saharan dust, were found to be higher based on the aerosol load than we observed in the SAL, further suggesting aging effects of INPs in the SAL.

Airborne observations of bioaerosol over the Southeast United States using a Wideband Integrated Bioaerosol Sensor

AbstractBiological aerosols represent a diverse subset of particulate matter that is emitted directly to the atmosphere in the form of (but not limited to) bacteria, fungal spores, pollens, viruses, and plant debris. These particles can have local air quality implications, but potentially play a larger climate role by acting as efficient ice nucleating particles (INPs) and cloud condensation nuclei. We have deployed a Wideband Integrated Bioaerosol Sensor on the NASA DC‐8 aircraft to (1) quantify boundary layer (BL) variability of fluorescent biological aerosol particle (FBAP) concentrations in the Southeast United States (SEUS), (2) link this variability explicitly to land cover heterogeneity in the region, and (3) examine the vertical profile of bioaerosols in the context of convective vertical redistribution. Flight‐averaged FBAP concentrations ranged between 0.1 and 0.43 scm−3 (cm−3 at standard temperature and pressure) with relatively homogeneous concentrations throughout the region; croplands showed the highest concentrations in the BL (0.37 scm−3), and lowest concentrations were associated with evergreen forests (0.24 scm−3). Observed FBAP concentrations are in generally good agreement with model parameterized emission rates for bacteria, and discrepancies are likely the result of fungal spore contributions. Shallow convection in the region is shown to be a relatively efficient lofting mechanism as the vertical transport efficiency of FBAP is at least equal to black carbon aerosol, suggesting that ground‐level FBAP survives transport into the free troposphere to be available for INP activation. Comparison of the fraction of coarse‐mode particles that were biological (fFBAP) suggested that the SEUS (fFBAP = 8.5%) was a much stronger source of bioaerosols than long‐range transport during a Saharan Air Layer (SAL) dust event (fFBAP = 0.17%) or summertime marine emissions in the Gulf of Mexico (fFBAP = 0.73%).

Abundance of fluorescent biological aerosol particles at temperatures conducive to the formation of mixed-phase and cirrus clouds

Abstract. Some types of biological particles are known to nucleate ice at warmer temperatures than mineral dust, with the potential to influence cloud microphysical properties and climate. However, the prevalence of these particle types above the atmospheric boundary layer is not well known. Many types of biological particles fluoresce when exposed to ultraviolet light, and the Wideband Integrated Bioaerosol Sensor takes advantage of this characteristic to perform real-time measurements of fluorescent biological aerosol particles (FBAPs). This instrument was flown on the National Center for Atmospheric Research Gulfstream V aircraft to measure concentrations of fluorescent biological particles from different potential sources and at various altitudes over the US western plains in early autumn. Clear-air number concentrations of FBAPs between 0.8 and 12 µm diameter usually decreased with height and generally were about 10–100 L−1 in the continental boundary layer but always much lower at temperatures colder than 255 K in the free troposphere. At intermediate temperatures where biological ice-nucleating particles may influence mixed-phase cloud formation (255 K ≤ T ≤ 270 K), concentrations of fluorescent particles were the most variable and were occasionally near boundary-layer concentrations. Predicted vertical distributions of ice-nucleating particle concentrations based on FBAP measurements in this temperature regime sometimes reached typical concentrations of primary ice in clouds but were often much lower. If convection was assumed to lift boundary-layer FBAPs without losses to the free troposphere, better agreement between predicted ice-nucleating particle concentrations and typical ice crystal concentrations was achieved. Ice-nucleating particle concentrations were also measured during one flight and showed a decrease with height, and concentrations were consistent with a relationship to FBAPs established previously at the forested surface site below. The vertical distributions of FBAPs measured on five flights were also compared with those for bacteria, fungal spores, and pollen predicted from the EMAC global chemistry–climate model for the same geographic region.

Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist Drugs

Although rhodopsin-like G protein-coupled receptors can exist as both monomers and non-covalently associated dimers/oligomers, the steady-state proportion of each form and whether this is regulated by receptor ligands are unknown. Herein we address these topics for the M1 muscarinic acetylcholine receptor, a key molecular target for novel cognition enhancers, by using spatial intensity distribution analysis. This method can measure fluorescent particle concentration and assess oligomerization states of proteins within defined regions of living cells. Imaging and analysis of the basolateral surface of cells expressing some 50 molecules·μm−2 human muscarinic M1 receptor identified a ∼75:25 mixture of receptor monomers and dimers/oligomers. Both sustained and shorter term treatment with the selective M1 antagonist pirenzepine resulted in a large shift in the distribution of receptor species to favor the dimeric/oligomeric state. Although sustained treatment with pirenzepine also resulted in marked up-regulation of the receptor, simple mass action effects were not the basis for ligand-induced stabilization of receptor dimers/oligomers. The related antagonist telenzepine also produced stabilization and enrichment of the M1 receptor dimer population, but the receptor subtype non-selective antagonists atropine and N-methylscopolamine did not. In contrast, neither pirenzepine nor telenzepine altered the quaternary organization of the related M3 muscarinic receptor. These data provide unique insights into the selective capacity of receptor ligands to promote and/or stabilize receptor dimers/oligomers and demonstrate that the dynamics of ligand regulation of the quaternary organization of G protein-coupled receptors is markedly more complex than previously appreciated. This may have major implications for receptor function and behavior.