River Water Samples Research Articles

Pollution Monitoring via Potentiometric Membrane Sensors for the Determination of Chlorpromazine Hydrochloride in the Presence of Its Main Photo-Degradation Products in River Water

The utilization of membrane sensors for the monitoring and determination of pharmaceutical environmental pollutants has emerged as a crucial objective in recent years. Given the extensive use of chlorpromazine hydrochloride (CPZ) in medicine, its presence in the environment, particularly in surface water such as rivers, is highly probable. Prolonged exposure of river water to sunlight and the photo-degradability of CPZ may enhance its photo-degradation. For the purpose of measuring CPZ in the presence of its primary photo-degradants, two sensitive and selective membrane electrodes were developed. These were synthesized utilizing two ion-pairing agents: sodium tetraphenylborate (TPB) and phosphotungstic acid (PTA). The electrodes exhibited a linear range that extended from 1 × 10−6 M to 1 × 10−2 M. The membrane electrodes of CPZ-TPB and CPZ-PTA exhibited slopes of 59.90 ± 0.60 mV/decade and 58.90 ± 0.80 mV/decade, respectively. The sensors mentioned above showed acceptable performance in a pH range of 2.0 to 6.0. All test parameters were optimized to provide superior electrochemical performance. The fabricated membranes were effectively employed to sensitively quantify CPZ in the presence of its principal photodegradants. The developed sensors were successfully employed to quantify CPZ in river water samples without necessitating pre-treatment procedures.

Land-Use Impacts on Soil Erosion: Geochemical Insights from an Urban Drinking Catchment, South-Central Chile

We investigate the influence of land use and land cover (LU/LC) changes on soil erosion and chemical weathering processes within the Nonguén watershed in the Coastal Cordillera of south-central Chile. The watershed is divided into three sub-basins, each characterized by distinct LU/LC patterns: native forest and exotic plantations. A comprehensive geochemical analysis, including trace elements and lithium (Li) isotopes, was conducted on river water and suspended sediment samples collected from streams within these sub-basins to assess how land management practices, particularly plantation activities, influence the geochemical composition of river systems. Our results show that sub-basins dominated by exotic plantations exhibit significantly higher concentrations of major and trace elements in suspended sediments compared to sub-basins dominated by native forests. The elevated trace element concentrations are primarily attributed to increased physical erosion due to forestry activities such as clear-cutting and soil disturbance, which enhance sediment mobilization. Notably, concentrations of elements such as Fe, Al, and As in plantation-dominated sub-basins are raised to ten times higher than in native-dominated sub-basins. In contrast, sub-basins with native forest cover exhibit lower levels of sediment transport and trace element mobilization, suggesting that native vegetation exerts a stabilizing effect that mitigates soil erosion. Despite the substantial differences in sediment transport and element concentrations, Li isotopic data (δ7Li) show minimal fractionation across the different LU/LC types. This indicates that land use changes impact the chemical weathering processes less compared to physical erosion. The isotopic signatures suggest that physical erosion, rather than chemical weathering, is the dominant process influencing trace element distribution in plantation-dominated areas. The study provides critical insights into how forestry practices, specifically the expansion of exotic plantations, accelerate soil degradation and affect the geochemical composition of river systems. The increased sediment loads, and trace element concentrations observed in plantation-dominated sub-basins, raise concerns about the long-term sustainability of forest management practices, particularly regarding their impacts on water quality in urban catchment areas. These results are of significant relevance for environmental management and policy, as they underscore the need for more investigation and sustainable land use strategies to minimize soil erosion and preserve water resources in regions undergoing rapid LU/LC changes.

The pangenome analysis of the environmental source Salmonella enterica highlights a diverse accessory genome and a distinct serotype clustering.

Salmonella remains the leading cause of foodborne infections globally. Environmental reservoirs, particularly aquatic bodies, serve as conduits for the fecal-oral transmission of this pathogen. While the gastrointestinal tract is traditionally considered the primary habitat of Salmonella, mounting evidence suggests the bacterium's capacity for survival in external environments. The application of advanced technological platforms, such as next-generation sequencing (NGS), facilitates a comprehensive analysis of Salmonella's genomic features. This study aims to characterize the genomic composition of Salmonella isolates from river water, contributing to a potential paradigm shift and advancing public health protection. A total of 25 river water samples were collected and processed, followed by microbiological isolation of Salmonella strains, which were then sequenced. Genomic characterization revealed adaptive mechanisms, including gene duplication. Furthermore, an open pangenome, predisposed to incorporating foreign genetic material, was identified. Notably, antibiotic resistance genes were found to be part of the core genome, challenging previous reports that placed them in the accessory genome.

Self-Powered Potentiometric Sensor with Relational Operation Function to Capture Concentration Excursions.

Self-powered potentiometric sensors spontaneously respond to activity changes of target species without the need for an external power source. Here, a self-powered potentiometric sensing approach is described that may store concentration perturbations that occur before the sensor readout through a combination of capacitors and diodes. Two channels, termed "more than" and "less than" operators, are utilized as memory modules in the sensor circuit to record positive and negative concentration excursions, respectively. Each channel is constructed with a capacitor-diode pair in which each diode is connected to a capacitor in the opposite direction to prevent unwanted capacitor discharge. With this design, only potential variations that agree with the polarity of the diode may pass and be stored in the capacitor. A limitation of the principle is that the conductivity of the diode is very small if the voltage across it diminishes over time as it approaches the equilibrium value. To address this, the forward voltage is increased by about 1 V by switching from an initial Ag/AgCl reference electrode (RE) to a Zn/Zn2+ element. The device may be used to monitor whether a concentration excursion has occurred in the time leading up to the signal readout in a semiquantitative manner. The approach also differentiates pH excursions of different durations (20, 40, 60 min). As an example, four different pH excursions of 20 min duration were successfully distinguished in river water samples with amplitudes of 1 to 4 pH units relative to the case without pH perturbation.

Hydrophobic deep eutectic solvent-ferrofluid microextraction followed by liquid chromatography-mass spectrometry for the enantioselective determination of chiral agrochemicals in natural waters.

The increasing use of chiral agrochemicals sold as racemic formulations raises concern for the negative impacts that inactive enantiomers can have on aquatic life and human health. The present work just focuses on the determination of ten chiral pesticides in river water samples by applying a ferrofluid-based microextraction followed by their stereoselective liquid chromatography analysis. To develop the ferrofluid, magnetite nanoparticles were prepared and coated with oleic acid and then dispersed in a hydrophobic natural deep eutectic solvent (NaDES), composed ofL-menthol and thymol (1:1). The stable colloidal dispersion was characterised by scanning electron microscopy, thermogravimetric analysis, energy-dispersive X-ray spectroscopy and attenuated total reflection Fourier transform infrared spectroscopy. The analyte microextraction from 5ml river samples was performed using 50µl of ferrofluid, while acidified acetonitrile (150µl) was used to break down the ferrofluid and solubilise the NaDES containing the analytes. All the extracts were analysed by high-performance liquid chromatography-tandem mass spectrometry. For each analyte, the baseline separation of isomers was achieved on a Lux i-Amylose-3 column (amylose tris(3-chloro-5-methylphenylcarbamate) working in reversed-phase mode; the combination with mass spectrometry detection allows the overall separation of 24 isomers (ten chiral analytes among which eight containing a single (one) chiral centre, one with two chiral centres and the last one existing in four stereoisomeric forms, due to the presence of two regioisomers with a chiral carbon) within 37min. The method showed very good figures of merit in terms of recoveries (77.7-97.5%), intra-day and inter-day precision (2.7-7.7% and 6.9-14.9%, respectively), limit of detection (0.01-0.35µg/L), limit of quantitation (0.03-1.20µg/L), linear dynamic range, and intra-day and inter-day accuracy (1.2-14.8% and 1.8-15.0%, respectively). The presented method was able to detect 14 out of 24 isomers at the preventive limit established by the Italian legislation for single pesticide (that for a chiral pesticide is the sum of all its isomers) in surface waters, set at 0.1µg/l. Finally, the method was evaluated using AGREEprep and ComplexGAPI metrics, compared with other ferrofluid-based methods, and applied to the analysis of water samples from two Italian rivers (the Nera River and the Tiber River), providing to be sustainable and reliable for the application to real river matrices.

Visual aptasensor based on PtNPs/g-C3N4 and DNase I for the field detection of acetamiprid.

A visual aptasensor based on the combination of graphitic carbon nitride loaded with platinum nanoparticles (PtNPs/g-C3N4) and deoxyribonuclease I (DNase I) was developed for detecting acetamiprid. The prepared PtNPs/g-C3N4 exhibited excellent peroxidase (POD)-like activity, demonstrating the capacity to oxidize the colourless o-phenylenediamine (OPD) to produce the coloured product diaminophenazine (DAP) in the presence of hydrogen peroxide (H2O2). The DNA aptamer of acetamiprid can adsorb onto the surface of PtNPs/g-C3N4, thereby inhibiting its POD activity. The binding of acetamiprid to its aptamer results in the aptamer desorbing from the surface of PtNPs/g-C3N4 and subsequent digestion by DNase I. Ascribed to the synergistic effect of these factors, the aptasensor can achieve the rapid on-site detection of acetamiprid based on the acetamiprid-induced the colour change of the solution just with the smartphone. Furthermore, due to the remarkable fluorescence signal of DAP at 570nm, the aptasensor under fluorescence mode enables highly sensitive and quantitative detection of acetamiprid with a linear range of 1 ng/mL to 4µg/mL and a detection limit as low as 0.31 ng/mL.Theaptasensor has successfully realized the detection of acetamiprid in river water and cucumber samples, offering a novel perspective for the rapid assessment of environmental pollution and food safety risks associated with acetamiprid residues.

Photoelectrochemical detection of Cu2+ based on ZnIn2S4/WO3 Z-scheme heterojunction.

A one-step hydrothermal technique was utilized to generate WO3 nanosheets on fluorine-doped tin oxide (FTO) (WO3/FTO), which were subsequently modified with ZnIn2S4 microspheres to create a Z-scheme heterojunction ZnIn2S4/WO3/FTO electrode for Cu2+ detection. The heterojunction exhibited excellent photoelectric conversion efficiency, which was nearly 2.5-fold and 5.1-fold greater than that ofWO3 and ZnIn2S4. The reduced photoelectrochemical response signal was caused by the formation of CuxSandenabled Cu2+ assessment in water samples. After optimizing the experimental conditions, the anodic photocurrent at 0V vs SCE in 0.100M phosphate buffer (pH 7.0) containing 0.100M L-ascorbic acid was linear with the common logarithm of Cu2+ concentration from 5.00nM to 100μM, with a limit of detection of 1.2nM (S/N = 3). Satisfactory recovery results were obtained in the analyses of Xiangjiang River water samples.

Tracing freshwater sources and particle discharge in Kongsfjorden: insights from a water isotope approach

Arctic fjords are inherently vulnerable to global warming, particularly because of the substantial freshwater influx resulting from the melting of glaciers. In this study, precipitation, river water, surface ice, and seawater samples from Kongsfjorden were collected to identify the main sources of freshwater. The dual water isotope (δ18O and δD) results and temperature–salinity profiles revealed that between 0% and 7% freshwater contributed to the fjord’s water. Furthermore, different freshwater sources for surface and deep water were identified by the dual water isotope analysis. Turbidity profiles confirmed the alter in particle discharge associated with surface runoff and subglacial discharge. Our study highlighted the sensitivity of water isotope analysis in elucidating the hydrological processes within the fjord system and demonstrated its potential for investigating the impact of meltwater on biological processes in the Arctic.

An MIP-Based PFAS Sensor Exploiting Nanolayers on Plastic Optical Fibers for Ultra-Wide and Ultra-Low Detection Ranges-A Case Study of PFAS Detection in River Water.

In this work, a novel optical-chemical sensor for the detection of per- and polyfluorinated substances (PFASs) in a real scenario is presented. The proposed sensing approach exploits the multimode characteristics of plastic optical fibers (POFs) to achieve unconventional sensors via surface plasmon resonance (SPR) phenomena. The sensor is realized by the coupling of an SPR-POF platform with a novel chemical chip based on different polymeric nanolayers over the core of a D-shaped POF, one made up of an optical adhesive and one of a molecularly imprinted polymer (MIP) for PFAS. The chemical chip is used to launch the light into the SPR D-shaped POF platform, so the interaction between the analyte and the MIP's sites can be used to modulate the propagated light in the POFs and the SPR phenomena. Selectivity tests and dose-response curves by standard PFOA water solutions were carried out to characterize the detection range sensor response, obtaining a wide PFAS response range, from 1 ppt to 1000 ppt. Then, tests performed on river water samples collected from the Bormida river paved the way for the applicability of the proposed approach to a real scenario.

Facile synthesis and fabrication of Mg2SnO4/carbon black as a sustainable electrode for determination of non-steroidal anti-inflammatory drug-flutamide

The accumulation of hazardous pharmaceutical wastes in aquatic organisms, particularly nonsteroidal anti-inflammatory drug molecules, has severe toxicological consequences for both aquatic life and humans. To protect the environment, it is essential to develop a highly efficient device with dual-purpose capabilities for drug detection while minimizing catalyst expenditure. In this work, we explored a simple and effective design for fabricating a magnesium stannate combined with carbon black (Mg2SnO4/CB) nanocomposite as a cost-effective, sustainable electrode material for the electrochemical detection of flutamide (Flu). The Mg2SnO4/CB nanocomposite was synthesized through a simple hydrothermal process followed by sonication. Various analytical methods were used to determine its physico-chemical characteristics. The electrochemical efficiency of Mg2SnO4/CB/GCE was evaluated by detecting Flu, showing a remarkable linear range from 0.6 to 198.4 µM with a sensitivity of 3.91 μA μM−1 cm−2. In addition, the constructed sensor demonstrated excellent selectivity, high repeatability, outstanding reproducibility, and long-lasting stability. The anti-interference experiments yielded a definite current response without any change in peak shifts. Consequently, Mg2SnO4/CB/GCE demonstrated superior performance in determining Flu in human urine and river water samples.

Green and Mild Fabrication of Magnetic Poly(trithiocyanuric acid) Polymers for Rapid and Selective Separation of Mercury(II) Ions in Aqueous Samples.

The removal and detection of highly toxic mercury(II) ions (Hg2+) in water used daily is essential for human health and monitoring environmental pollution. Efficient porous organic polymers (POPs) can provide a strong adsorption capacity toward heavy metal ions, although the complex synthetic process and inconvenient phase separation steps limit their application. Hence, a combination of POPs and magnetic nanomaterials was proposed and a new magnetic porous organic polymer adsorbent was fabricated by a green and mild redox reaction in the aqueous phase with trithiocyanuric acid (TA) and its sodium salts acting as reductive monomers and iodine acting as an oxidant. In the preparation steps, no additional harmful organic solvent is required and the byproducts of sodium iodine are generally considered to be non-toxic. The resulting magnetic poly(trithiocyanuric acid) polymers (MPTAPs) are highly porous, have large surface areas, are rich in sulfhydryl groups and show easy magnetic separation ability. The experimental results show that MPTAPs exhibit good adsorption affinity toward Hg2+ with high selectivity, rapid adsorption kinetics (10 min), a large adsorption capacity (211 mg g-1) and wide adsorption applicability under various pH environments (pH 2~8). Additionally, MPTAPs can be reused for up to 10 cycles, and the magnetic separation step of MPTAPs is fast and convenient, reducing energy consumption compared to centrifugation and filtration steps required for non-magnetic adsorbents. These results demonstrate the promising capability of MPTAPs as superior adsorbents for effective adsorption and separation of Hg2+. Based on this, the prepared MPTAPs were adopted as magnetic solid-phase extraction (MSPE) materials for isolation of trace Hg2+ from aqueous samples. Under optimized conditions, the extraction and quantification of trace Hg2+ in water samples were accomplished using inductively coupled plasma mass spectrometry (ICP-MS) detection after MSPE procedures. The proposed MPTAPs-based MSPE-ICP-MS method is efficient, rapid, sensitive and selective for the determination of trace Hg2+, and was successfully employed for the accurate analysis of trace Hg2+ in tap water, wastewater, lake water and river water samples.

A 3D (3,3,5)-connected Cd(II) MOF as multiresponsive fluorescent sensor of CrO42−, Cr2O72− and dipicolinic acid

Metal-organic frameworks (MOFs) have received great attention in fluorescent sensing application due to their good stability, short response time and maneuverability. Cr(VI) oxo-anions (CrO42− and Cr2O72−) are highly toxic ions for environment water. 2,6-dipicolinic acid (DPA) is the specific biomarker of Bacillus anthracis. Therefore, the exploration of multi-functional fluorescence sensors for detection Cr(VI) oxo-anions and DPA is very necessary. In this work, we synthesized a fluorescent Cd(II) MOF for detection of CrO42−, Cr2O72− and DPA in aqueous solution. The Cd(II) MOF formulated as {[Cd2(bpda)(bbimh)0.5(H2O)4]·H2O}n (1) was constructed by 2,3,3′,4′-biphenyltetracarboxylic acid (H4bpda) mixed with 1,6-bis(benzimidazole)hexane (bbimh). MOF 1 presents a three-dimensional (3D) framework with unusual trinodal (3,3,5)-connected topology. MOF 1 shows effective sensing ability for detection CrO42−, Cr2O72− and DPA via fluorescence quenching effect in aqueous solution with the detection limits being 0.96 μM, 0.94 μM and 1.68 μM, respectively. The quenching mechanisms were elucidated by powder X-ray diffraction (PXRD), UV–vis spectra, lifetimes and theoretical calculations. Furthermore, MOF 1 was also applied to detect CrO42− and Cr2O72− in river water sample and DPA in serum sample. This work provides an effective MOF as multifunctional sensor toward water pollutants and biomarker.

Simple solution and paper-based fluorescent aptasensors for toxic metal ions, thallium(l) and lead(ll).

Heavy metal ions, such as thallium(I) and lead(II) are environmental toxicants known to cause a severe threat to human and ecosystem health. This work investigates aptamers and intercalating chromophore-based complexes for the detection of these toxic species. In one method, a selective label-free "turn-on" biosensor was developed using a G-quadruplex-intercalating agent, berberine. Fluorescence, melting temperature (Tm), and circular dichroism analysis confirmed the affinity and selectivity results, illustrating the potential of these aptasensor methods for improving detection limits. These fluorescence assays were found to perform with a detection limit of 3.4 μM for Tl(I) and 0.84 nM for Pb(II). Furthermore, the assays were challenged successfully with Tl(I) and Pb(II) spiked into river water samples. We next developed paper-based fluorescent assays for Tl(I) and Pb(II), where the aptamer/berberine complex was spotted onto the paper test zone. When Tl(I) or Pb(II) ions solutions were spotted onto the top of the test zone and the spot was illuminated with a portable UV light (365 nm), a strong green fluorescence could be easily visualized with the naked eye. The lowest detection limits achieved with these fluorescent paper-based assays for Tl(I) and Pb(II) were 1.1 nM and 1.6 nM, respectively. The two fluorescent approaches presented here have the potential to be the basis of rapid, fast, and cost-efficient screening assays for these toxic species.

Electrospun Nanofiber Dopped with TiO2 and Carbon Quantum Dots for the Photocatalytic Degradation of Antibiotics.

Novel photocatalysts were synthesized through the association of carbon quantum dots (CQDs) with commercial (P25) titanium dioxide (TiO2) by sonication. The resulting TiO2/CQDs composite was then incorporated into the polyamide 66 (PA66) biopolymer nanofibers using the electrospinning technique, considering a composite nanoparticles-to-polymer ratio of 1:2 in the electrospinning precursor solution. The produced nanofibers presented suitable morphology and were tested for the photocatalytic degradation under simulated solar radiation of 10 mg L-1 of amoxicillin (AMX) and sulfadiazine (SDZ), in phosphate buffer solution (pH 8.06) and river water, using 1.5 g L-1 of photocatalyst. The presence of the photocatalyst increased the removal of AMX in phosphate buffer solution by 30 times, reducing the AMX degradation half-life time from 62 ± 1 h (without catalyst) to 1.98 ± 0.06 h. Moreover, SDZ degradation half-life time in phosphate buffer solution was reduced from 5.4 ± 0.1 h (without catalyst) to 1.87 ± 0.05 h in the presence of the photocatalyst. Furthermore, the PA66/TiO2/CQDs were also efficient in river water samples and maintained their performance in at least three cycles of SDZ photodegradation in river water. The presented results evidence that the produced photocatalyst can be a promising and sustainable solution for antibiotics' efficient removal from water.

Distributions of Fecal Indicators at Aquaculture Areas in a Bay of Republic of Korea.

Aquaculture products, such as clams, scallops, and oysters, are major vectors of fecal-derived pathogens. Male-specific and somatic coliphages are strongly correlated with human noroviruses, the major enteric viruses worldwide. Geographic information system with local land-use patterns can also provide valuable information for tracking sources of fecal-derived pathogens. We examined distributions of four fecal indicator microorganisms, i.e., male-specific and somatic coliphage, total coliform, and Escherichia coli (E. coli) in three river and seawater sampling sites located on the coast of Gomso Bay in the Republic of Korea during the sampling period (from March 2015 to January 2016). Geospatial analyses of fecal indicators and correlation between environmental parameters and fecal indicators or among fecal indicators were also performed. Overall, river water samples showed highest concentrations of both types of coliphage in summer (July 2015). High concentrations of both total coliform and E. coli were detected in river water during the period from July to September 2015. High concentrations of all fecal indicators were found at site GL02, located in the innermost part of Gomso Bay, which has high-density agriculture and residential areas. Environmental factors related to precipitation-cumulative precipitation on and from 3 days before the sampling day (Prep-0 and Prep-3, respectively)-and salinity were strongly correlated with concentrations of all fecal indicators. The present results suggest that investigations of multiple fecal indicators with a systemic geospatial information are necessary for precisely tracking fecal contaminations of aquaculture products.

Application of Fabric Phase Sorptive Extraction as a Green Method for the Analysis of 10 Anti-Diabetic Drugs in Environmental Water Samples

Due to the increased prevalence of diabetes, the consumption of anti-diabetic drugs for its treatment has likewise increased. Metformin is an anti-diabetic drug that is commonly prescribed for patients with type 2 diabetes and has been frequently detected in surface water and wastewaters, thus representing an emerging contaminant. Metformin can be prescribed in combination with other classes of anti-diabetic drugs; however, these drugs are not sufficiently investigated in environmental samples. Fabric phase sorptive extraction (FPSE) has emerged as a simple and green method for the extraction of analytes in environmental samples. In this study, FPSE coupled with a high-performance liquid chromatography diode array detector (HPLC-DAD) was employed for the simultaneous analysis of different classes of anti-diabetic drugs (metformin, dapagliflozin, liraglutide, pioglitazone, gliclazide, glimepiride, glargine, repaglinide, sitagliptin, and vildagliptin) in environmental water samples. Four different fabric membranes were synthesized but the microfiber glass filter coated with sol-gel polyethylene glycol (PEG 300) was observed to be the best FPSE membrane. The parameters affecting the FPSE process were optimized using a combination of one-factor-at-a-time processes and the design of experiments. The FPSE was evaluated as a green extraction method, based on green sample preparation criteria. The FPSE-HPLC-DAD method achieved acceptable validation results and was applied for the simultaneous analysis of anti-diabetic drugs in surface and wastewater samples. Glimepiride was detected below the quantification limit in both lake and river water samples. Dapagliflozin, liraglutide, and glimepiride were detected at 69.0 ± 1.0 μg·L−1, 71.9 ± 0.4 μg·L−1, and 93.9 ± 1.3 μg·L−1, respectively, in the city wastewater influent. Dapagliflozin and glimepiride were still detected below the quantification limit in city wastewater effluent. For the hospital wastewater influent, metformin and glimepiride were detected at 1158 ± 21 μg·L−1 and 28 ± 0.8 μg·L−1, respectively, while only metformin (392.6 ± 7.7 μg·L−1) was detected in hospital wastewater effluent.

Enhanced Pb(II) extraction using a novel chitosan/pectin/carbon composite adsorbent for solid-phase extraction

ABSTRACT This research aimed to present the development of chitosan/pectin/carbon (CPC) materials as adsorbents in the solid-phase extraction (SPE) of Pb(II) from river water samples. The CPC adsorbent shows active groups effectively binding Pb(II) ions. The characterisation included using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (SEM-EDX) to analyse functional groups and evaluate surface morphology with elemental composition. SPE parameters were systematically optimised to enhance adsorption-desorption efficiency, including pH 4.0, Pb(II) concentration of 5 mg L−1, flow rate of 13.3 mL min−1, elution flow rate of 12.8 mL/min using nitric acid (HNO3), a sample volume of 25 mL, eluent volume of 1 mL and concentration at 1.0 M. The results showed that the implementation of the refined CPC-based SPE method for Pb(II) analysis in water samples obtained a recovery range of 101% to 103%, accompanied by a significant 25-fold concentration enrichment of Pb(II). Moreover, the adsorption concentration increased from undetectable levels to 1.27–2.48 mg L−1, reporting the efficacy of the CPC-based SPE method for sensitive and accurate Pb(II) analysis in environmental samples.

Portable paper-based multicolor sensor for sensitive on-site detection of organophosphorus pesticides using a high-efficiency Au+-induced gold nanobipyramids aspect ratio regulation strategy

On-site visual detection of organophosphorus pesticides (OPs) is crucial for safeguarding environmental and food safety. This study presents a robust, sensitive, and portable paper-based multicolor sensor (PMS) for the on-site detection of OPs. The PMS involves a novel Au+-induced gold nanobipyramids (AuNBPs) morphology transformation reaction within a paper-based analytical device (PAD) coupled with a bienzymatic hydrolysis system. The Au+-induced reaction sensitively regulates the aspect ratio of AuNBPs through Au+ disproportionation, which decreases the length of AuNBPs and simultaneously increases the width, accompanied by distinct multicolor changes. Upon performing in the PAD incorporating easily-prepared AuNBPs-deposited nylon membranes, a metal heater, and an oscillator, the Au+-induced reaction exhibits excellent reaction sensitivity, efficiency, reproducibility, AuNBPs stability, and color uniformity. In the bienzymatic hydrolysis system, acetylcholinesterase (AChE) and choline oxidase hydrolyze acetylcholine to product H2O2, which consumes tris(2-carboxyethyl)phosphine hydrochloride (TCEP), maintaining free Au+ for the disproportionation in the Au+-induced system, while the presence of OPs inhibits AChE activity, preserving TCEP to chelate Au+ and hindering the disproportionation. Under optimized conditions, the PMS exhibited eight dichlorvos concentration-corresponding color changes with a visual detection limit of 30 μg/L and a spectrometry detection limit of 8.1 μg/L. It achieved recoveries of 85.4–101.9 % in river water, drinking water, rice, and Chinese cabbage samples with relative standard deviations (n = 5) < 6 %. Thus, this study offers a portable, sensitive, reliable, and practical on-site detection method for OPs. Additionally, the proposed Au+-induced AuNBPs morphology transformation system within the PAD offers promising alternative strategies for developing other AuNBPs-based colorimetric sensors.

Prevalence of antibiotic resistance genes in bacteria from Gomti and Ganga rivers: implications for water quality and public health.

Rivers serve as a significant habitat and water sources for diverse organisms, including humans. An important environmental and public health concern is the increase in antibiotic-resistant bacteria (ARBs) and genes (ARGs) in aquatic ecosystems brought about by excessive pollutant flow. The research highlighted that river water, which is receiving discharge from wastewater treatment plants, is harbouring multidrug-resistant bacteria. River water samples were collected in January, April, July and October 2022 from three separate locations of each Gomti and Ganga river. A total of 114 bacteria were isolated from Gomti as well as the Ganga River. All the isolates were tested for their resistance to various antibiotics by disc diffusion method. The isolated bacteria were tested for the antibiotic resistance genes using PCR and were identified by 16s rRNA sequencing. The ARBs percentages for each antibiotic were as follows: ampicillin (100%); cefotaxime (96.4, 63.1%); erythromycin (52.6, 57.8%); amikacin (68.4, 50.8%); tetracycline (47.3, 54.3%); nalidixic acid (47.3, 45.6%); streptomycin (68.4, 49.1%); gentamycin (43.8, 35%); chloramphenicol (26.3, 33.3%); neomycin (49.1, 29.8%) and ciprofloxacin (24.5, 7.01%). Further, antibiotic resistance genes in Gomti and Ganga water samples disclose distinctive patterns, including resistance to ermB (25, 40%); tetM (25, 33.3%); ampC (44.4, 40%) and cmlA1 (16.6%). Notably cmlA1 resistant genes were absent in all bacterial strains of the Gomti River. Additionally, gyrA gene was not found in both the river water samples. The presence of ARGs in the bacteria from river water shows threat of transferring these genes to native environmental bacteria. To protect the environment and public health, constant research is necessary to fully understand the extent and consequences of antibiotic resistance in these aquatic habitats.

Heavy Metal Identification in Water Resources and the Surrounding Environment of the Cirasea Riparian Zone, Indonesia

The Cirasea River can provide water for both the Bandung basin and agricultural irrigation. Intensive agriculture, industry, and land use changes could have an impact on water quality. The purpose of this study is to look at the origins of heavy metals in riparian water resources. Heavy metal analysis was performed on 13 groundwater and river water samples. Heavy metals in water sources were compared with sediment and soil. The samples were analyzed for heavy metals using an AAS instrument. The research method employs statistical, geographical, and heavy metal pollution index (HPI). The HPI for river water was 131, whereas groundwater was 93. River water with an HPI value of more than 100 is highly polluted, indicating that it is unsafe for human consumption and has negative health consequences. Data verification with heavy metals in sediments reveals the presence of heavy metals coming from geogenic circumstances in various locations in the upstream area. Heavy metals in downstream areas result from geological factors and anthropogenic activities in the surrounding area. The long-term effects of heavy metal pollution along the riparian zone will become apparent. More research is needed on communities that depend on groundwater supplies along the Cirasea watershed.