Passive Sampling Techniques Research Articles

Profiling and assessing soil-air exchange of polycyclic aromatic hydrocarbons (PAHs) in playground dust and soil using ex situ equilibrium passive sampling

Cancer risk can be associated with exposure to polycyclic aromatic hydrocarbons (PAHs) in playground dust and soil. This study investigated the profiles and sources of PAHs from poured rubber-surfaced playground dust and uncovered playground surface soil, by applying an ex-situ equilibrium passive sampling technique. Surface dust and soil samples were collected from 15 different playgrounds in Seoul, Republic of Korea. The total 16 EPA PAHs concentrations in surface dust and soil varied from 198 to 919 μg kg−1 dw and 68–169 μg kg−1 dw, respectively. 4- to 6-ring PAHs were dominant, accounting for approximately 53.8%–94.5% of the total PAHs in surface dust and soil. The diagnostic ratios and principal component analysis suggested that a mixed coal combustion and vehicular emission was likely the main source of PAHs in the surface dust and soil. The higher total organic carbon content can explain the higher PAH accumulation and lower fugacities of PAHs. The fugacity comparison of phenanthrene and pyrene in dust, soil, air, and playground surface material indicated that atmospheric deposition is the main source of PAHs in the dust and soil on rubber-surfaced and uncovered surfaced playgrounds. This study contributes to the understanding of PAHs sources in dust and soil samples in children's playground and helps policymaker determine the right contamination sources for risk management.

Metal Removal by a Free Surface Constructed Wetland and Prediction of Metal Bioavailability and Toxicity with Diffusive Gradients in Thin Films (DGT) and Biotic Ligand Model (BLM).

The H-02 constructed wetland is a free water surface wetland to remove copper (Cu) and zinc (Zn) from the industrial wastewater. In this study, we evaluated the performance of the wetland from 2018 to 2019 and coupled the diffusive gradients in thin films (DGTs) and biotic ligand model (BLM) to explore metal speciation and bioavailability in wetland waters. Surface water samples were collected and piston DGTs were deployed in different sites of the wetland. The H-02 wetland functioned well during the sampling period with high removal efficiencies (Cu: 73.8 ± 1.2% and Zn: 75.2 ± 16.0%). In our study, with the assumption that the combination of BLM predicted inorganic metals species, BLM Cu(II) and BLM Zn(II), were the bioavailable and toxic species, DGT-Cu did not correlate to BLM Cu(II) (P = 0.47), but DGT-Zn positively correlated to BLM Zn(II) (R2 = 0.35, P < 0.001). Compared to the modeling results of BLM, DGT-indicated labile and/or bioavailable Cu included not only free Cu ions and inorganic Cu complexes but also a high percentage of Cu-labile organic matter complexes. DGT-indicated Zn included free Zn ion, inorganic Zn, and only a low percentage of Zn-labile organic matter complexes. Our findings illustrated the appropriate use of passive sampling techniques and geological modeling when biomonitoring could be substituted. The close monitoring of metal concentrations, speciation, and bioavailability helps us understand metal biogeochemistry and metal removal processes and ensure the long-term sustainability of the constructed wetland.

Seasonal variations of cadmium (Cd) speciation and mobility in sediments from the Xizhi River basin, South China, based on passive sampling techniques and a thermodynamic chemical equilibrium model

Understanding the speciation and mobilization mechanisms of potentially toxic metals in sediments is critical to aquatic ecosystem health and contamination remediation in urban rivers. In this study, chemical sequential extraction, a thermodynamic chemical equilibrium model (Visual MINTEQ ver. 3.1), diffusive gradient in thin films (DGT), and high-resolution dialysis (HR-Peeper) techniques were integrated to identify seasonal variations in cadmium (Cd) mobility in sulfidized sediments. Acid-soluble Cd was the dominant geochemical fraction in sediments, followed by residual, oxidizable, and reducible Cd. The DGT-labile Cd concentration was associated with various geochemical processes and was independent of the total concentration and geochemical fractionation of Cd in sediments. Sulfate reduction facilitated the formation of insoluble CdS and induced low Cd concentrations in sediment porewater. Sulfide oxidation was principally responsible for lowered porewater pH and elevated Cd concentrations in summer. Strongly acidic conditions promoted release of sediment Cd but might reduce the binding efficiency of Chelex resin gel for dissolved Cd, leading to underestimation of the mobility of sediment Cd. Sediments generally functioned as a sink for Cd in winter and shifted to acting as a source in summer, releasing Cd into the overlying water mainly as Cd-S complexes with high potential to migrate downstream.

Distribution of Freely Dissolved Polycyclic Aromatic Hydrocarbons in the Yellow Sea: Application of Improved Passive Sampling Technique

Distribution of Freely Dissolved Polycyclic Aromatic Hydrocarbons in the Yellow Sea: Application of Improved Passive Sampling Technique

SPECIATION AND QUANTIFICATION OF LABILE HEAVY METAL DISCHARGES IN OGUN RIVERS USING DGT TECHNIQUE.

This study profiled labile exogenous metals ubiquitous in the ecology of Ogun River induced by persistent anthropogenic activities along the riverbanks. The labile metals existing as metal-ions were trapped with a passive sampling technique of diffused gradients in thin films (DGT) subsequent upon which the metal-ions were carefully extracted and analyzed using the Atomic Absorption Spectroscopy (AAS). Nine labile metals (Pb, Cd, Ni, Cr, Co, Cu, Mn, Fe and Zn) were targeted in this study. The results of the study showed that mean values of labile Fe and Zn exceeded 3 µg/L whilst those of labile Pb, Cd and Mn occurred in the range of 1.41 and 1.88 µg/L in the river matrices. The mean values of labile Cr, Co, Ni and Cu occurred below 1.0 µg/L in the river matrices. The high industrial activities and population density along the Isheri, Ilo and Owo axes of the Ogun River accentuated the presence of labile Pb, Zn and Fe in the river matrices.

In situ arsenic speciation at the soil/water interface of saline-alkaline lakes of the Pantanal, Brazil: A DGT-based approach

Arsenic (As) is a naturally occurring element in the Earth's crust, exhibiting toxicity towards a wide range of living organisms. Its properties and environmental dynamics are strongly regulated by its speciation, and the species As(III) and As(V) are the most commonly found in environmental systems. Recently, high concentrations of As were found in saline-alkaline lakes of the Pantanal (Brazil), which is the largest wetland area in the world. Therefore, we evaluated As contamination and its redox speciation (As(III) and As(V)) at the soil/water interface of biogeochemically distinct saline-alkaline lakes of Pantanal wetlands (Brazil). Both conventional sampling and in situ diffusive gradients in thin films (DGT) technique were employed. Zirconium oxide and 3-mercaptopropyl were used as ligand phases in DGT to selectively bind As species. High concentrations of total dissolved As in a shallow water table were found (<2337.5 μg L−1), whereas levels in soils were up to 2.4 μg g−1. Distinct scenarios were observed when comparing speciation analysis through spot sampling and DGT. Considering spot sampling, As(V) was the main species detected, whereas As(III) was only detected in only a few samples (<4.2 μg L−1). Conversely, results obtained by DGT showed that labile As(III) dominated arsenic speciation at the soil/water interface with levels up to 203.0 μg L−1. Coupling DGT data and DGT induced fluxes in sediments and soils model allowed obtaining kinetic data, showing that the soil barely participated in the arsenic dynamics on the shore of the lakes, and that this participation depends on the evapoconcentration process occurring in the region. Therefore, soil acts like a nonreactive matrix depending on the natural concentration process. In addition, our results reinforced the different geochemical characteristics of the studied saline-alkaline lakes and highlights the importance of robust passive sampling techniques in the context of metal/metalloid speciation in environmental analysis.

Field comparison of passive polyurethane foam and active air sampling techniques for analysis of gas-phase semi-volatile organic compounds at a remote high-mountain site

Polyurethane foam passive air samplers (PUF-PAS) are good candidates for the determination of gas-phase semi-volatile organic compound (SVOC) air concentrations in high-mountain areas over long periods because they do not require an energy supply. However, the harsh meteorological conditions present in such locations can increase the uncertainties inherently associated to PAS sampling rates due to the many variables involved in their calculation and to the assumptions made regarding PUF diffusive uptake mechanics, which can considerably bias the resulting concentrations. Therefore, we studied the performance of PUF-PASs in a remote location in the Pyrenees mountain range for the analysis of several SVOCs in air, including polychlorobiphenyls (PCBs), hexachlorobenzene, pentachlorobenzene, polycyclic aromatic hydrocarbons (PAHs), and the less studied emerging organophosphate flame retardants (OPFRs). An in-situ PUF-PAS calibration using Performance Reference Compounds (PRCs) provided compound- and sampler-specific sampling rates, showing mean experimental errors (12%) that adequately conformed to an estimate of their expanded theoretical uncertainties (15%). This showcases the suitability of this calibration strategy in an area with conditions beyond those typically considered in calibration efforts available to date. Moreover, gas-phase concentrations of the studied pollutants from PUF-PAS samples showed very good agreement (R2 up to 0.91, p < 0.01) when compared to those obtained using a conventional high-volume active air sampler (PUF-AAS), with some minor deviations observed for PAHs caused by the seasonality in their atmospheric concentrations. No relevant levels of pollutants preferentially bound to the particle phase were detected in the PUF-PASs, the particle infiltration efficiency of the sampler configuration used was found to be low, and compounds typically distributed between the gas and particle phases of AAS samples revealed profiles consistent with their vapor pressures, except for some OPFRs.

Identification of Antibiotics in Surface-Groundwater. A Tool towards the Ecopharmacovigilance Approach: A Portuguese Case-Study.

Environmental monitoring, particularly of water, is crucial to screen and preselect potential hazardous substances for policy guidance and risk minimisation strategies. In Portugal, extensive data are missing. This work aimed to perform a qualitative survey of antibiotics in surface- groundwater, reflecting demographic, spatial, consumption and drug profiles during an observational period of three years. A passive sampling technique (POCIS) and high-resolution chromatographic system were used to monitor and analyse the antibiotics. The most frequently detected antibiotics were enrofloxacin/ciprofloxacin and tetracycline in surface-groundwater, while clarithromycin/erythromycin and sulfamethoxazole were identified only in surface water. The detection of enzyme inhibitors (e.g., tazobactam/cilastatin) used exclusively in hospitals and abacavir, a specific human medicine was also noteworthy. North (Guimarães, Santo Tirso and Porto) and South (Faro, Olhão and Portimão) Portugal were the regions with the most significant frequency of substances in surface water. The relatively higher detection downstream of the effluent discharge points compared with a low detection upstream could be attributed to a low efficiency in urban wastewater treatment plants and an increased agricultural pressure. This screening approach is essential to identify substances in order to perform future quantitative risk assessment and establishing water quality standards. The greatest challenge of this survey data is to promote an ecopharmacovigilance framework, implement measures to avoid misuse/overuse of antibiotics and slow down emission and antibiotic resistance.

Passive Sampling of SARS-CoV-2 for Wastewater Surveillance.

The shedding of pathogens by infected humans enables the use of sewage monitoring to conduct wastewater-based epidemiology (WBE). Although most WBE studies use data from large sewage treatment plants, timely data from smaller catchments are needed for targeted public health action. Traditional sampling methods, like autosamplers or grab sampling, are not conducive to quick ad hoc deployments and high-resolution monitoring at these smaller scales. This study develops and validates a cheap and easily deployable passive sampler unit, made from readily available consumables, with relevance to the COVID-19 pandemic but with broader use for WBE. We provide the first evidence that passive samplers can be used to detect SARS-CoV-2 in wastewater from populations with low prevalence of active COVID-19 infections (0.034 to 0.34 per 10,000), demonstrating their ability for early detection of infections at three different scales (lot, suburb, and city). A side by side evaluation of passive samplers (n = 245) and traditionally collected wastewater samples (n = 183) verified that the passive samplers were sensitive at detecting SARS-CoV-2 in wastewater. On all 33 days where we directly compared traditional and passive sampling techniques, at least one passive sampler was positive when the average SARS-CoV-2 concentration in the wastewater equaled or exceeded the quantification limit of 1.8 gene copies per mL (n = 7). Moreover, on 13 occasions where wastewater SARS-CoV-2 concentrations were less than 1.8 gene copies per mL, one or more passive samplers were positive. Finally, there was a statistically significant (p < 0.001) positive relationship between the concentrations of SARS-CoV-2 in wastewater and the levels found on the passive samplers, indicating that with further evaluation, these devices could yield semi-quantitative results in the future. Passive samplers have the potential for wide use in WBE with attractive feasibility attributes of cost, ease of deployment at small-scale locations, and continuous sampling of the wastewater. Further research will focus on the optimization of laboratory methods including elution and extraction and continued parallel deployment and evaluations in a variety of settings to inform optimal use in wastewater surveillance.

Tetrafluoroterephthalonitrile-crosslinked β-cyclodextrin polymer as a binding agent of diffusive gradients in thin-films for sampling endocrine disrupting chemicals in water

β-Cyclodextrin (β-CD) is an inexpensive and reproducible material derived from corn starch. It is possible that tetrafluoroterephthalonitrile-crosslinked β-cyclodextrin polymer (TFN-CD), a cheap but efficient adsorbent, could be a suitable binding agent for use in the passive sampling technique, diffusive gradients in thin-films (DGT). Herein, the TFN-CD binding gel was prepared and then evaluated as the binding phase of DGT to sample six endocrine disrupting chemicals (EDCs) in water. The TFN-CD dispersed uniformly in the binding gel due to its hydrophilicity. The quantitative recoveries (99.3%–106%) of EDCs from the TFN-CD binding gel could be conveniently achieved by ultrasonic extraction using 5 mL methanol for 10 min. Compared with the excellent HLB (hydrophilic-lipophilic-balanced resin) binding gel, the TFN-CD binding gel had comparable or even faster adsorption kinetics, although the equilibrium adsorption capacity was slightly lower. The effective adsorption capacities of TFN-CD-based DGT (TFN-CD-DGT) were roughly estimated to enable a 7-days deployment in EDC solution of 25.7–30.0 μg L−1. Studies of influencing factors showed that the ionic strength (0–0.5 M), pH (3.73–9.13), dissolved organic matter (0–20 mg L−1) and long-term storage (204 days) had negligible influence on the performance of TFN-CD-DGT. Finally, the TFN-CD-DGT was successfully used to record sudden increases in bulk concentrations during simulated discharge events in pond water. These results demonstrate that TFN-CD is a suitable binding agent for sampling of EDCs, and the low cost of TFN-CD could be conducive to the application of DGT in large-scale sampling.

Bromeliad Sampling: A Passive Technique for Arboreal Amphibians across Ecosystems in the Neotropics

Bromeliads are recognized as vital habitats for arboreal amphibians. However, these plants are often not included in traditional amphibian surveys. Furthermore, focused canopy sampling techniques are time-consuming, require specialized equipment and training, and, in the case of bromeliads, sampling is typically destructive. In this study, we developed and tested a new passive sampling technique for amphibians in bromeliads, which can be easily implemented in common amphibian surveys in the Neotropics. Our study was conducted in five different forests along an elevation gradient (0–2,200 m a.s.l.) in the central region of Veracruz, Mexico. In each forest, 15 tank bromeliads were relocated on large trees at 1.5 m above the ground (n = 75) by fastening them onto metal rings attached to the trees. Over a period of one year, these bromeliads were inspected monthly for amphibians. In total, we recorded 34 individuals belonging to eight species, including small and rare species that are normally difficult to find in the field. This technique appears to be effective in detecting frogs and salamanders across a range of ecosystems, especially in the cloud and mangrove forest where they were found more frequently throughout the year. Bromeliad relocation represents an alternative sampling technique for arboreal amphibians, which reduces the number of bromeliads that have to be sacrificed, requires few resources and minimal prior knowledge, and can be implemented effectively in studies that need repeated sampling through time.

Field application of a novel active-passive sampling technique for the simultaneous measurement of a wide range of contaminants in water

A first test of the field capabilities of a novel in situ sampling technique combining active and passive sampling (APS) was conducted in the sea. The proof-of-concept device uses a pump to draw water into a diffusion cell where dissolved target substances are accumulated onto sorbents which are selective for different classes of contaminants (i.e., metal cations, polar and non-polar organic compounds), simultaneously. A controlled laminar flow established in the diffusion cell enables measurements of contaminant concentrations that are fully independent from the hydrodynamic conditions in the bulk solution. APS measurements were consistent with those obtained using conventional passive sampling techniques such as organic diffusive gradients in thin films (o-DGT) and silicone rubber (SR) samplers (generally < 40% difference), taking into account the prevailing hydrodynamic conditions. The use of performance reference compounds (PRC) for hydrophobic contaminants provided additional information. Field measurements of metal ions in seawater showed large variability due to issues related to the device configuration. An improved field set-up deployed in supplementary freshwater mesocosm experiments provided metal speciation data that was consistent with passive sampling measurements (DGT), taking into account the hydrodynamic conditions. Overall, the results indicate that the APS technique provides a promising approach for the determination of a wide range of contaminants simultaneously, and independently from the hydrodynamic conditions in the bulk solution.

Assessing variability in the ratio of metal concentrations measured by DGT-type passive samplers and spot sampling in European seawaters

The current study evaluates the effect of seawater physico-chemical characteristics on the relationship between the concentration of metals measured by Diffusive Gradients in Thin films (DGT) passive samplers (i.e., DGT-labile concentration) and the concentrations measured in discrete water samples. Accordingly, Inductively Coupled Plasma Mass Spectrometry (ICP-MS) was used to measure the total dissolved metal concentrations in the discrete water samples and the labile metal concentrations obtained by DGT samplers; additionally, lead and cadmium conditional labile fractions were determined by Anodic Stripping Voltammetry (ASV) and total dissolved nickel was measured by Cathodic Stripping Voltammetry (CSV). It can be concluded that, in general, the median ratios of DGT/ICP and DGT/ASV(CSV) were lower than 1, except for Ni (median ratio close to 1) and Zn (higher than 1). This indicates the importance of speciation and time-integrated concentrations measured using passive sampling techniques, which is in line with the WFD suggestions for improving the chemical assessment of waterbodies. It is the variability in metal content in waters rather than environmental conditions to which the variability of the ratios can be attributed. The ratios were not significantly affected by the temperature, salinity, pH, oxygen, DOC or SPM, giving a great confidence for all the techniques used. Within a regulatory context such as the EU Water Framework Directive this is a great advantage, since the simplicity of not needing to use corrections to minimize the effects of environmental variables could help in implementing DGTs within monitoring networks.

Trends and applications in plant volatile sampling and analysis.

Volatile organic compounds (VOCs) released by plants serve as information and defense chemicals in mutualistic and antagonistic interactions and mitigate effects of abiotic stress. Passive and dynamic sampling techniques combined with gas chromatography-mass spectrometry analysis have become routine tools to measure emissions of VOCs and determine their various functions. More recently, knowledge of the roles of plant VOCs in the aboveground environment has led to the exploration of similar functions in the soil and rhizosphere. Moreover, VOC patterns have been recognized as sensitive and time-dependent markers of biotic and abiotic stress. This focused review addresses these developments by presenting recent progress in VOC sampling and analysis. We show advances in the use of small, inexpensive sampling devices and describe methods to monitor plant VOC emissions in the belowground environment. We further address latest trends in real-time measurements of volatilomes in plant phenotyping and most recent developments of small portable devices and VOC sensors for non-invasive VOC fingerprinting of plant disease. These technologies allow for innovative approaches to study plant VOC biology and application in agriculture.

Assessment of pesticides in water using time-weighted average calibration of passive sampling device manufactured with carbon nanomaterial coating on stainless steel wire.

The continued contamination of water sources by pesticides is a problem that involves the life of aquatic organisms and human health, especially in countries whose economy is based on agriculture. The need to know the quality of drinking water under these circumstances is a priority for the public health of any community. Passive sampling methods allow the determination of long-term environmental pollutants through a single sample collection, reducing time and cost of analyses. One advantage of passive sampling is that it is possible to calculate a time-weighted average (TWA) concentration value or an equilibrium concentration value, depending on the type of device used and the exposure time. Passive sampling techniques using carbon nanomaterials (CNMs) have a high potential for pesticide sampling in aquatic systems. A device for passive sampling manufactured with CNMs in a microextraction system and recyclable materials was calibrated in laboratory exposure conditions over 15days. The calibration results showed linear accumulation periods between 5 and 10days. Sampling rates were between 0.014 and 0.146mL day-1. The sampler was field-tested in the San Francisco river basin in the state of Minas Gerais in Brazil for 7days. This research allowed for the detection and calculation of TWA concentrations for organochlorine pesticides such as α-HCH, 4,4-DDE, and 4,4-DD in water sources. The manufactured device demonstrated greater sensitivity than the grab sampling processes for the detection of pesticides. The performed passive sampling system using gas chromatography/mass spectrometry (GC/MS) technique allowed for the collection, detection, identification, and quantification of 26 pesticides.

Determination of low-density polyethylene–water partition coefficients for novel halogenated flame retardants with the large volume model and co-solvent model

The partition coefficient (Kpew) of an analyte between low-density polyethylene (LDPE) film and water is a critical parameter for measuring freely dissolved concentrations of the analyte with PE passive sampling devices. Measuring log Kpew for super hydrophobic organic chemicals (HOCs) have been proven extremely difficult. The present study developed a large volume model for measuring log Kpew of super HOCs, i.e., novel halogenated flame retardants (NHFRs). Results showed that the measured log Kpew values of selected PAHs and PCBs obtained by the large volume model were in line with those from the co-solvent model and the literature data within less 0.3 log units of difference, while those of NHFRs (6.27–7.34) except for hexachlorocyclopentadienyldibromocyclooctane (HCDBCO) and Decabromodiphenyl ethane (DBDPE) were significantly lower than those (6.51–8.89) from the co-solvent model. A curvilinear relationship was observed between log Kpew and log Kow of all target compounds, with the turning point at log Kow = ∼8.0 in the large volume model, but that was not found for the co-solvent model. These can be attributed to the large molecular volumes (> 450 Å3) for NHFRs, which require high Gibbs free energy to penetrate into the inside structures of LDPE in the large volume model. However, the solvent swelling effects in the co-solvent model needs to be investigated. Therefore, the large volume model is robust to determine the Kpew values of super HOCs for facilitating the application of aquatic passive sampling techniques.

Static renewal and continuous-flow calibration of two types of passive samplers for the monitoring of pharmaceuticals in wastewater

Passive sampling techniques are becoming increasingly popular in monitoring of micropollutants. They are especially important to track semipolar and polar contaminants, such as pharmaceuticals. The proper calibration of passive samplers is the key to obtain accurate time-weighted average concentrations (TWAC) of pharmaceuticals in the environment. This paper aims to compare two calibration systems: static renewal and continuous-flow, on the obtained sampling rates of selected pharmaceuticals (atenolol, caffeine, sulfamethoxazole, carbamazepine, naproxen, diclofenac). Two passive sampling techniques were investigated: Passive Sampling by Ionic Liquids (PASSIL) with phosphonium ionic liquid as the receiving phase, and home-made Polar Organic Chemical Integrative Sampler (POCIS). We report the first in-situ trial conducted for the ionic liquid-based sampler in treated wastewater, simultaneously with POCIS deployment. Generally, there was agreement between the TWAC and average concentration of pharmaceuticals from grab samples. For PASSIL the best match was observed with the static renewal calibration system, while for POCIS the use system of calibration had no effect on the agreement of the values. These results show that the calibration system has an impact into accuracy of TWAC measurement.

Health Risk Assessment of Residents in a Tourist City: A Case Study of Nakhon Si Thammarat Province

Nakhon Si Thammarat is one of the most popular tourist destinations among the secondary tourism cities according to economic promotions. The rapid growth of the tourism industry is evidenced by increasing road traffic, especially at weekends, contributing to high nitrogen dioxide (NO2) concentration. The concentration of NO2 was measured in the main tourist destinations of Nakhon Si Thammarat Province. Likewise, health risks from NO2 exposure were also evaluated for the local residents. Air mass movement was applied to indicate risk areas of non-cancer health effects from exposure to NO2. Air samples were collected over 24 hours using a passive sampling technique at 3 areas in the tourist destination on weekdays and weekends during the wet season in 2018 and 2019. Results showed that NO2 concentrations at weekends were 2 - 3 times higher than on weekdays due to increased vehicular traffic. Anthropogenic activities had a greater influence than meteorological conditions on pollutant concentration. The NO2 concentration was within the ambient air quality standard, but toxicological risk quotients for the residents were above the recommended limits for human health. Findings indicated that local residents risked non-cancer health effects from long-term exposure to NO2. Therefore, sensitive residents should avoid outdoor activities on weekends. Moreover, the tourism authority should consider controlling visitor numbers, providing a parking area, and providing public transportation systems to reduce traffic-related pollutants for sustainable tourism in Thailand.

Aerosols Generated during Endodontic Treatment: A Special Concern during the Coronavirus Disease 2019 Pandemic

IntroductionThe aims of this study were to investigate aerosolized microorganisms generated during endodontic emergencies and nonsurgical root canal therapy (NSRCT), to assess the spread of airborne microbes, and to verify the spatial distribution of airborne microbial spread. MethodsA total of 45 endodontic procedures were sampled, including full pulpotomy (n = 15), pulpectomy (n = 15), and NSRCT (n = 15). Samples were collected during room resting and after treatment. The passive air sampling technique using settle plates was applied. Agar plates were set at different locations in the operatory. The colony-forming unit (CFU) was counted in brain-heart infusion blood agar plates. A set of agar plates containing selective chromogenic culture media was used for the isolation and presumptive identification of target microorganisms. Fungi were investigated using Sabouraud dextrose agar. ResultsPulpotomy generated the lowest mean CFU count (P < .05). There was no difference between the mean CFU counts found in pulpectomy and NSRCT (P > .05). A higher mean CFU count was found close to the patient's mouth (0.5 m) than at a 2-m distance in pulpectomy and NSRCT (P < .05). There was no difference between the mean CFU count found in front of the patient's mouth versus diagonal in pulpectomy and NSRCT (P > .05). Staphylococcus aureus (22/45, 48.8%) was the most frequent bacteria species. Longer treatment times were associated with higher CFU counts. ConclusionsOur findings indicated that pulpotomy generates less aerosolized microorganisms than pulpectomy and NSRCT. The proximity to the patient's mouth and the treatment duration were implicated in the level of contamination.

Application of diffusive gradients in thin-films in sediments and soils

Diffusive gradients in thin-films (DGT) is an in situ passive sampling technique that can measure heavy metals, nutrients and organics in the environment. It has the advantages of species selectivity, high resolution and getting the average concentration during the monitoring period, and it has been widely used in sediments and soils. This paper introduced the device and principle of DGT, and reviewed the application progress of DGT in sediments and soils. It was suggested that DGT was an efficient and available method for the in situ high resolution measurement and prediction of the bioavailability of heavy metals. Finally, the future development of the DGT was prospected.