Analysis Of Environmental Samples Research Articles

Sulfolane Analysis in Environmental Samples: A Critical Review

Sulfolane, a highly water-soluble industrial solvent, has raised environmental concerns due to its widespread usage and its prolonged persistence once released into the environment. To assess the extent of contamination effectively, reliable analytical methods are essential. In this review article, the existing methodologies for the sample preparation and determination of sulfolane are systematically examined and evaluated. In brief, existing guidelines for sampling from environmental matrices provide a solid foundation for sulfolane analysis. Notably, there is little variation in the choice of final determination methods, with GC-MS or GC-FID being favored across all studies. However, substantial variability emerges in sample preparation methods. Moreover, upon scrutiny of the analytical procedures utilized in sulfolane analysis, it becomes evident that a considerable number of them are characterized by inefficiency or environmental hazards, often relying on substantial quantities of chlorinated solvents. Through this review, valuable insights into the challenges at hand and potential solutions can be gained, offering a foundation for the development of novel sulfolane analysis methods applicable to a range of environmental matrices. Overall, this field calls for further research to devise efficient and environmentally sustainable analytical methods for sulfolane analysis.

Alterations of Glycan Composition in Aerobic Granular Sludge during the Adaptation to Seawater Conditions.

Bacteria can synthesize a diverse array of glycans, being found attached to proteins and lipids or as loosely associated polysaccharides to the cells. The major challenge in glycan analysis in environmental samples lies in developing high-throughput and comprehensive characterization methodologies to elucidate the structure and monitor the change of the glycan profile, especially in protein glycosylation. To this end, in the current research, the dynamic change of the glycan profile of a few extracellular polymeric substance (EPS) samples was investigated by high-throughput lectin microarray and mass spectrometry, as well as sialylation and sulfation analysis. Those EPS were extracted from aerobic granular sludge collected at different stages during its adaptation to the seawater condition. It was found that there were glycoproteins in all of the EPS samples. In response to the exposure to seawater, the amount of glycoproteins and their glycan diversity displayed an increase during adaptation, followed by a decrease once the granules reached a stable state of adaptation. Information generated sheds light on the approaches to identify and monitor the diversity and dynamic alteration of the glycan profile of the EPS in response to environmental stimuli.

Smartphone readable three dimensional printed analytical kit for on-site detection of Cr(VI)

A rapid and easy-used colorimetric method was developed for on-site and rapid analysis of Cr(VI). Under acidic condition, Cr(VI) was reacted with 1, 5-diphenylcarbazide (DPC) and a purple-red complex was formed subsequently, inducing the color changed from colorless to purple-red, this color variance can be detected by ultraviolet–visible spectrophotometer (UV–Vis), smartphone and even naked-eye. For realizing the goal of on-site analysis, this method was integrated in a three dimensional (3D) printed analytical kit, smartphone was used as a portable detector. Under the optimized conditions, limit of detections (LODs) of 0.0014 μg/mL and 0.0016 μg/mL were obtained by smartphone and UV–Vis, respectively. Concentration of Cr(VI) as low as 0.05 μg/mL was still visible by naked-eye. This colorimetric system was further applied to the analysis of several environmental water samples, recoveries of 90–107 % were obtained. It is a promising portable analytical device/system for Cr(VI) on-site and rapid analysis.

Recent radiation protection activities related to nuclear facilities on the Iberian Peninsula

Part of the radiation protection in Spain and Portugal is focused on the protection of workers, public and environment due to the influence of nuclear facilities present in their territory (Spanish case) or nearby. Radiation protection is in a process of continuous improvement, with the participation of nuclear facilities, companies and researchers in numerous research projects funded in Spain by the Nuclear Safety Council or other international organizations. This article presents some of the projects in which Spanish working groups have participated. In addition, specific examples of activities related to radiation protection and environmental radiological monitoring carried out in Spain in recent years are shown. Among them are: the development of methods of analysis of environmental samples in case of emergency, real-time monitoring networks for measuring radiation, environmental dosimetry in the environment of nuclear facilities, programs and models of radiation dispersion in case of accident, and the treatment and management of radioactive waste for its clearance.

Insights into emerging organic pollutants extraction from polypropylene, polystyrene, and polyethylene microplastics

BackgroundMicroplastics have the capability of retaining contaminants on their surface, increasing their persistence, preconcentrating them, and acting as transport vectors. Nevertheless, the determination of these compounds in plastic matrices poses several analytical issues and challenges, including the capability of many of these methods of only determining the extractable pollutants fractions, repeatability issues, etc. In this sense, it is primordial to evaluate the effect of the critical parameters that allow to obtain a quantitative extraction of the target analytes from microplastics, including the matrix effect of each of the studied polymers, the influence of particle size, and the effect of weathering. ResultsA simple and effective methodology for the extraction of 17 emerging organic pollutants from both pristine (polypropylene, polystyrene, and low- and high-density polyethylene) and weathered (polypropylene and polyethylene) microplastics has been developed, optimized, and validated, achieving recovery values of 70–120 % and low method quantification limits (9.2–35.5 ng/g). Results show the importance of cryomilling microplastics (as smaller particle sizes improve recovery and homogenization), something ignored in most publications. The differences in matrix effect for the studied pristine polymers highlights the importance of treating polymers individually, without extrapolating results. In weathered microplastics, matrix effect is overall higher than in their pristine counterparts, evidencing the necessity of always carrying out matrix effect and recovery studies in environmental microplastics. The analysis of 10 samples collected in Playa Grande (Tenerife, Canary Islands, Spain) revealed quantitative amounts of bisphenol A (10.8 ± 3.4 ng/g) in one of them. SignificanceFor the first time, the effect of particle size, weathering and matrix effect have been simultaneously evaluated on microplastics, revealing the importance of their assessment to properly validate the methodology. Additionally, the method shows good performance in all the different polymers and has been successfully applied to the analysis of environmental samples of microplastics.

Dispersive micro-solid phase extraction based on graphene oxide for the ultrasensitive determination of Cd by slurry sampling microplasma optical emission spectrometry

For the first time, a dispersive micro-solid phase extraction (D-µSPE) based on graphene oxide was employed for the ultrasensitive determination of Cd by a solution anode glow discharge optical emission spectrometry (SAGD OES). It was possible to extract Cd from a dilute mixture of alkali and alkaline earth metals (Ca, K, Mg, and Na) with 100 % efficiency. It was found that in contact with microplasma, Cd bounded on the GO surface can be converted to its volatile species. As a result, it was possible to omit the elution step (a slurry sample was introduced), which allowed shortened time of sample preparation and reduced the risk of contamination. Using the Design of Experiments (DoE) approach, the effect of different variables, i.e., interferent concentration, GO concentration, number of GO rinsing repetitions, and HNO3 concentration, was studied in detail. Using the D-µSPE-SAGD OES, matrix effects were remarkably reduced and improvement in the tolerance of Cd to alkali metals by a factor of 25 was reached. Moreover, coupling with D-µSPE lowered the limit of detection (LOD) of Cd by 2 times (resulting in the LOD of 0.003 µg L−1). Under optimal operating conditions, D-µSPE-SAGD OES was successfully employed for the ultra-trace analysis of food and environmental samples characterized by a high-alkali metals content, i.e., wine and seawater. As compared to competitive methods recently reported in the literature, D-µSPE-SAGD OES is distinguished by the simplicity of the measurement system and the fact that the nanosorbent used is commercially available.

Platinum vaporization-deposition coated polycarbonate membranes for comprehensive, multimodal, and correlative microscopic analysis of micro-and nanoplastics and other environmental particles

Anthropogenic particles, including microplastics, are receiving ever-increasing concern due to their potential environmental impact. Surveys and monitoring require sampling from many environmental and biological matrices, including natural water, drinking water, sediment, and air. However, there are no standard methods for sampling particles in the environment; thereby, many different approaches are used for both single particle and ensemble distribution or bulk chemical analyses. In the microplastics field, particles are often analyzed on membranes using automated analysis with spectroscopic techniques such as Fourier-transform infrared spectroscopy (FTIR) and Raman spectroscopy. For automated analysis, the filters' properties are crucial. We coated polycarbonate (PC) membranes with 100 nm platinum (Pt) on both side using a e-beam evaporator and evaluated their suitability for filtrating and analysis of environmental samples. The PC membranes have a defined and practical pore size, available in many pore sizes and with circular diameter of 47 mm and 25 mm. Our Pt coated membranes can handle large volumes of fresh and marine waters, high pressure, and various treatment solutions. Moreover, they have good optical properties for imaging with light microscopy (LM) and Scanning Electron Microscopy (SEM), and no disturbing background signal for Raman or FTIR spectroscopy analysis.

Adaptive traits of cysts of the snow alga Sanguina nivaloides unveiled by 3D subcellular imaging

Sanguina nivaloides is the main alga forming red snowfields in high mountains and Polar Regions. It is non-cultivable. Analysis of environmental samples by X-ray tomography, focused-ion-beam scanning-electron-microscopy, physicochemical and physiological characterization reveal adaptive traits accounting for algal capacity to reside in snow. Cysts populate liquid water at the periphery of ice, are photosynthetically active, can survive for months, and are sensitive to freezing. They harbor a wrinkled plasma membrane expanding the interface with environment. Ionomic analysis supports a cell efflux of K+, and assimilation of phosphorus. Glycerolipidomic analysis confirms a phosphate limitation. The chloroplast contains thylakoids oriented in all directions, fixes carbon in a central pyrenoid and produces starch in peripheral protuberances. Analysis of cells kept in the dark shows that starch is a short-term carbon storage. The biogenesis of cytosolic droplets shows that they are loaded with triacylglycerol and carotenoids for long-term carbon storage and protection against oxidative stress.

Investigation of potential polyatomic interferences on uranium isotope ratio measurements for the LS-APGD-Orbitrap MS system

The determination of actinide (e.g., U and Pu) content and isotopics is of importance to the nuclear forensics and safeguards communities. However, in the analysis of environmental samples, such as those collected by the International Atomic Energy Agency, uranium measurements can be complicated by isobaric interferences from polyatomic variants of heavy elements (e.g., Pb). This leads to complex, time-consuming sample manipulations (i.e., separations) before determining isotope ratios. An alternative strategy to sample pretreatment is to use high-resolution mass spectrometric platforms during the analysis to fully resolve the uranium isotopes from potential polyatomic interferences, negating the need for prior chemical separation. The liquid sampling - atmospheric pressure glow discharge (LS-APGD) coupled with an Orbitrap mass spectrometer provides a high-resolution (>70,000 m/Δm at m/z 200) inorganic mass spectrometry platform. As a demonstration of the power of this instrumental platform, and indeed, the high-resolution approach in general, uranium isotope ratios were determined in the presence of elemental impurities (e.g., Pb, Pt, Ta, W) commonly encountered with environmental sample swipe analysis, without any prior treatment. Even at elemental impurity concentrations of 1000–5000× relative to uranium, no interference was observed with the 235U or 238U signal. In addition, the 235U/238U isotope ratio for the samples with the concomitants present are within 2 standard deviations of the values obtained without their addition, indicating that these impurities do not impact the determined uranium isotope ratio. These findings represent a significant first step in leveraging the high resolution of the LS-APGD-Orbitrap-MS to overcome isobaric and molecular interferences instead of relying on chemical separations.

Tunnel vision in the drinking water research field – Time for non-targeted analysis implementation?

A plethora of compounds can reach our drinking water and possibly affect human health. Still, mostly notorious pollutants like pesticides and disinfection by-products are monitored and regulated. With the increasing availability of high-resolution mass spectrometers (HRMS), non-targeted analyses of environmental samples have become possible. Pilot studies demonstrating the applicability of this approach in the drinking water research field were published. We would like to highlight these studies and appeal to researchers focused on water quality to better exploit the potential of HRMS instruments and broaden the scale of studied pollutants. In addition, the data and experience should be further shared, and the quality standard for the analytical procedures should be set. With advanced knowledge of compounds reaching the drinking water, potential threats would be revealed, and the comprehensive results on water pollution might also act as impulses for associated research branches, including toxicity assessment or development of water treatment technologies, and/or for policy-making.

Water-soluble polymers: Emerging contaminants detected, separated and quantified by a novel GPC/MALDI-TOF method

Water-soluble polymers (WSPs) are additives used as thickeners, stabilisers and flocculants in industry and in household products, including personal care products. Given their widespread use, it is likely WSPs enter the environment, particularly through wastewaters. This is of concern as there is little ecotoxicological research on their fate and behaviour once in the environment, which means their risk to aquatic life is not understood. The lack of suitable analytical techniques to detect, characterise and quantify WSPs hinders research on the potential impact of these polymers. A novel method has been developed that identifies polymers within a sample and separates them using gel-permeation chromatography (GPC). This is coupled with matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS), to quantify the polymer fractions using molecular weight information. This process has been carried out on a range of aqueous media. Polyethylene glycol (PEG) ingredients were successfully separated from non-polymeric material in a commercial shaving gel personal care product (PCP), before being quantified at 1.62 wt%. This method was applied to a spiked wastewater influent sample to demonstrate the extraction and separation of PEG from organic constituents such as dissolved organic matter (DOM). This highlighted the additional challenges of analysing WSPs in the environment, as factors such as sorption and biodegradation affected the total recovery of PEG, with an extraction efficiency of 53%. Overall, this method was applied for the extraction of PEG from a PCP with accurate quantification, before a proof-of-concept extraction from wastewater demonstrated the difficulties associated with WSP analysis in environmental samples. This method provides opportunities to use tandem GPC/MALDI-TOF MS to quantify WSPs in a broad array of environmental samples. Additional studies could include its application to wastewater or freshwater monitoring.

Simultaneous detection of As(III/V), Cr(III/VI), and Fe(II/III) by a sensor array based on the morphology regulation of CeO2 oxidase.

To develop a convenient method for simultaneous detection of As(III/V), Cr(III/VI), and Fe(II/III), three morphologies of CeO2 oxidase have been prepared. Based on the difference in oxidase activity and binding ability with substrate TMB of CeO2of different morphologies, a 3 (Signal unit) × 6 (Target number) × 5 (Repetition) sensor array was constructed to realize simultaneous detection of six variable valence metal ions As(III/V), Cr(III/VI), and Fe(II/III). The lowestdetection limit of the array for metal ions was 1.68µg/L. The analysis of environmental samples with multiple metal ions (binary and ternary mixtures) co-existing has confirmed that the sensor array can achieve simultaneous qualitative and quantitative results for composite samples. This study not only revealed the influencing factors of crystal morphology regulation on oxidase activity, but also provided a scheme for the morphology detection of easily convertible metal ions in the field through the construction of the sensor array.

3D printed stir bar sorptive extraction coupled with high performance liquid chromatography for trace estrogens analysis in environmental water samples

BackgroundAny imaginary shape with good preparation reproducibility can be made by 3D printing technology, and it has been applied in various fields. Comparatively, its applications in sample pre-treatment are relatively less, most of which involves making extraction sorbents and producing non-functionalized devices for support assistance. 3D printing has not been applied to fabricate stir bars in stir bar sorptive extraction, mainly due to the lacking of suitable printing feedstocks. This work aimed to fabricate stir bars by 3D printing, reducing the manufacturing cost and steps and improving preparation reproducibility. (90) ResultsBy using fused deposition modeling technique and porous filament printing feedstock, stir bars were fabricated without any modifications. Adsorption performance of 3D printed stir bars were investigated for substances with different structures and polarities. Five estrogens with adsorption efficiencies of over 80 % were selected as the representatives. The 3D printed stir bars exhibited good preparation reproducibility (2.9–4.4 %) and higher extraction recoveries (73–81 %) for five estrogens than commercial polydimethylsiloxane coated stir bars (13–69 %) in a shorter time (90 vs 120 min). They showed long lifespan (160 times) with good mechanical properties and merited reduced manufacturing cost (0.064 $ per bar) and manual operation. A method of stir bar sorptive extraction coupled with high performance liquid chromatography was proposed for trace analysis of estrogens in environmental water. Under the optimized conditions, the linear ranges for estrogens were 0.5–200 μg/L with LODs of 0.13–0.17 μg/L. (136) SignificanceThe feasibility of fused deposition modeling in stir bar fabrication was demonstrated, along with the potential of porous filament printing feedstock as the sorbent for substances with medium polarity. 3D printed stir bars were featured with excellent preparation reproducibility, long lifespan, and good mechanical properties. The stir bar fabrication method can be used for mass production with minimal differences in products performance. (62)

Low-field, not low quality: 1D simplification, selective detection, and heteronuclear 2D experiments for improving low-field NMR spectroscopy of environmental and biological samples.

Understanding environmental change is challenging and requires molecular-level tools to explain the physicochemical phenomena behind complex processes. Nuclear magnetic resonance (NMR) spectroscopy is a key tool that provides information on both molecular structures and interactions but is underutilized in environmental research because standard "high-field" NMR is financially and physically inaccessible for many and can be overwhelming to those outside of disciplines that routinely use NMR. "Low-field" NMR is an accessible alternative but has reduced sensitivity and increased spectral overlap, which is especially problematic for natural, heterogeneous samples. Therefore, the goal of this study is to investigate and apply innovative experiments that could minimize these challenges and improve low-field NMR analysis of environmental and biological samples. Spectral simplification (JRES, PSYCHE, singlet-only, multiple quantum filters), selective detection (GEMSTONE, DREAMTIME), and heteronuclear (reverse and CH3/CH2/CH-only HSQCs) NMR experiments are tested on samples of increasing complexity (amino acids, spruce resin, and intact water fleas) at-high field (500 MHz) and at low-field (80 MHz). A novel experiment called Doubly Selective HSQC is also introduced, wherein 1H signals are selectively detected based on the 1H and 13C chemical shifts of 1H-13C J-coupled pairs. The most promising approaches identified are the selective techniques (namely for monitoring), and the reverse and CH3-only HSQCs. Findings ultimately demonstrate that low-field NMR holds great potential for biological and environmental research. The multitude of NMR experiments available makes NMR tailorable to nearly any research need, and low-field NMR is therefore anticipated to become a valuable and widely used analytical tool moving forward.

Synthesis of porous organic framework materials based on deep eutectic solvents and their application in solid-phase extraction

This paper reviews the application of deep eutectic solvents (DESs) in the synthesis of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) as well as their prospects in the field of solid-phase extraction (SPE). Porous organic frameworks (POFs) have unique properties such as a large specific surface area, high porosity, and easy modification. Thus, these materials are widely applied in the fields of catalysis, adsorption, drug delivery, gas storage, and separation. POFs include MOFs, COFs, conjugated microporous polymers (CMPs), porous aromatic frameworks (PAFs), and covalent triazine frameworks (CTFs). MOFs are constructed from metal ions/clusters and organic ligands through coordination bonds and can be extended in two or three dimensions by repeated coordination with potential voids. COFs are formed from two monomers containing light elements (such as carbon, hydrogen, oxygen, nitrogen, boron, and other elements) via coordination bonds and have large two- or three-dimensional structures. However, conventional POF synthesis methods generally suffer from disadvantages such as long synthesis times, high temperature and pressure requirements, and the use of toxic and hazardous reaction solvents. DES consists of a hydrogen bond acceptor (HBA) and a hydrogen bond donor (HBD) bound by hydrogen-bonding interactions. It is a promising green solvent for material synthesis owing to its low vapor pressure, high stability, and ease of preparation. DES can be used to prepare MOFs and COFs and, in specific cases, acts as a structure-directing agent, which has an important impact on the structure and properties of the resulting frameworks. Using appropriate DES formulations, researchers can modulate the crystal structures, pore sizes, and surface properties of MOFs and COFs, resulting in materials with excellent characteristics. SPE is an analytical technique in which a sample solution is added to an SPE column; the sample solution is forced through the stationary phase, and the target compounds are collected for analysis by elution with an organic solvent. Therefore, suitable stationary-phase materials are critical for SPE. Owing to their large specific surface areas and abundant active sites, MOFs and COFs exhibit outstanding adsorption capacity and selectivity in SPE and can effectively enrich target analytes from complex samples. DES-based MOFs and COFs have shown potential use in a wide range of applications, such as in environmental analysis, food testing, and biological sample analysis. Although DES-based MOFs and COFs for SPE are still in the early stages of development, their properties such as efficient enrichment and high selectivity offer good prospects for practical applications. Future research should continue to explore DES-based synthesis methods in depth to prepare other MOFs and COFs with the desired properties and investigate their potential applications in various fields. These efforts are expected to apply these novel materials in commercialized solid-phase extraction methods, bringing new development opportunities in the field of analytical chemistry.

Solid-Phase Microextraction Techniques and Application in Food and Horticultural Crops.

Solid-phase microextraction (SPME) is a sample preparation technique which utilizes small amounts of an extraction phase for the extraction of target analytes from investigated sample matrices. Its simplicity of use, relatively short sample processing time, and fiber reusability have made SPME an attractive choice for many analytical applications. SPME has been widely applied to the sampling and analysis of environmental, food, aromatic, metallic, forensic, and pharmaceutical samples. Solid phase microextraction is used in horticultural crops, for example, to determine water and soil contaminants (pesticides, alcohols, phenols, amines, herbicides, etc.). SPME is also used in the food industry to separate biologically active substances in food products for various purposes, for example, disease prevention, determining the smell of food products, and analyzing tastes. SPME has been applied to forensic analysis to determine the alcohol concentration in blood and that of sugar in urine. This method has also been widely used in pharmaceutical analysis. It is a solvent-free sample preparation technique that integrates sampling, isolation, and concentration. This review focuses on recent work on the use of SPME techniques in the analysis of food and horticultural crops.

Dual sorbent coating based magnet-integrated fabric phase sorptive extraction as a front-end to gas chromatography–mass spectrometry for multi-class pesticide determination in water samples

Magnet-integrated fabric phase sorptive extraction (MI-FPSE) is a sample preparation technique that has proved to be a powerful tool for environmental analysis. The fabrication and application of magnet-integrated dual sorbent-based FPSE membrane prepared by combining two different sol-gel sorbent-coated disks of different polarities together with a magnetic bar inserted between the two membranes to allow the stirring, was examined as novel preparation technique that not required samples pretreatments. The dual sorbent-based sample preparation platforms (made up of poly(tetrahydrofuran) and Carbowax 20M) were used for the extraction of seven classes of pesticides from ambient surface water samples prior to their determination by gas chromatography–mass spectrometry. Initially, different single and dual sol-gel sorbent-based MI-FPSE membranes were evaluated in terms of their extraction efficiency. The MI-FPSE with dual sol-gel sorbents were found to be superior to the single-materials MI-FPSE devices in terms of extraction recovery. The main parameters affecting the MI-FPSE extraction protocol (e.g., adsorption time, sample volume, stirring rate, salt addition, eluent type, desorption time and elution volume) were investigated. The selected extraction protocol enabled detection limits in the range between 0.001 and 0.16 ng mL−1. Furthermore, good relative standard deviation values for the intra-day and inter-day repeatability studies were obtained and were lower than 5.9 and 9.9 %, respectively. The proposed method was successfully used for the multi-class analysis of environmental surface water samples.

Development of Low-Magnetic Susceptibility Microcoils via 5-Axis Machining for Analysis of Biological and Environmental Samples.

In environmental research, it is critical to understand how toxins impact invertebrate eggs and egg banks, which, due to their tiny size, are very challenging to study by conventional nuclear magnetic resonance (NMR) spectroscopy. Microcoil technology has been extensively utilized to enhance the mass-sensitivity of NMR. In a previous study, 5-axis computer numerical control (CNC) micromilling (shown to be a viable alternative to traditional microcoil production methods) was used to create a prototype copper slotted-tube resonator (STR). Despite the excellent limit of detection (LOD) of the resonator, the quality of the line shape was very poor due to the magnetic susceptibility of the copper resonator itself. This is best solved using magnetic susceptibility-matched materials. In this study, approaches are investigated that improve the susceptibility while retaining the versatility of coil milling. One method involves machining STRs from various copper/aluminum alloys, while the other involves machining ones from an aluminum 2011 alloy and electroplating them with copper. In all cases, combining copper and aluminum to produce resonators resulted in improved line shape and SNR compared to pure copper resonators due to their reduced magnetic susceptibility. However, the copper-plated aluminum resonators showed optimal performance from the devices tested. The enhanced LOD of these STRs allowed for the first 1H-13C heteronuclear multiple quantum coherence (HMQC) of a single intact 13C-labeled Daphnia magna egg (∼4 μg total biomass). This is a key step toward future screening programs that aim to elucidate the toxic processes in aquatic eggs.

Rational Construction of V2O5 with Functionalized MWCNTs: An Efficient Electron Transfer Electrode Material for Facile Detection of N-acetyl-p-aminophenol

N-acetyl-p-aminophenol, commonly known as paracetamol (PAL), is a widely prescribed drug for the treatment of fever and moderate pain. The presence of PAL at trace levels has been detected in hospital wastewater, drinking water, and sewage water, primarily due to its excretion from human and animal urine. Therefore, this work intends to improve the detection of PAL in human urine, thereby boosting its monitoring and analysis in environmental samples. Here in we developed a rational construction of the nanoflake structured vanadium pentoxide (V2O5) particles with functionalized multiwalled carbon nanotube [V2O5@f-MWCNT (1–4)] and evaluated their electrocatalytic performance for the detection of PAL. The synthesized materials were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and Field emission scanning electron microscopy (FE-SEM) with elemental mapping analysis. The electrocatalytic performance of different electrocatalysts on the GCE surface was studied through cyclic voltammetry (CV) and differential pulse voltammetry (DPV). It was observed that the optimized V2O5@f-MWCNT-3 nanocomposite exhibited higher electrocatalytic activity towards PAL, resulting in a wide linear range of detection. The respectable limit of detection (LOD) of the V2O5@f-MWCNT-3 modified GCE was found to be 0.00185 μM and utilized for analyzing PAL in real samples.

Metagenomic Analysis of Environmental Samples from Wildlife Rescue Station at Poyang Lake, China

ObjectiveTo improve the understanding of the virome and bacterial microbiome in the wildlife rescue station of Poyang Lake, China. MethodsTen smear samples were collected in March 2019 Metagenomic sequencing was performed to delineate bacterial and viral diversity. Taxonomic analysis was performed using the Kraken2 and Bracken methods. A maximum-likelihood tree was constructed based on the RNA-dependent RNA polymerase (RdRp) region of picornavirus. ResultsWe identified 363 bacterial and 6 viral families. A significant difference in microbial and viral abundance was found between samples S01–S09 and S10. In S01–S09, members of Flavobacteriia and Gammaproteobacteria were the most prevalent, while in S10, the most prevalent bacteria class was Actinomycetia. Among S01–S09, members of Myoviridae and Herelleviridae were the most prevalent, while the dominant virus family of S10 was Picornaviridae. The full genome of the pigeon mesivirus-like virus (NC-BM-233) was recovered from S10 and contained an open reading frame of 8,124 nt. It showed the best hit to the pigeon mesivirus 2 polyprotein, with 84.10% amino acid identity. Phylogenetic analysis showed that RdRp clustered into Megrivirus B. ConclusionThis study provides an initial assessment of the bacteria and viruses in the cage-smeared samples, broadens our knowledge of viral and bacterial diversity, and is a way to discover potential pathogens in wild birds