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The assessment of the ecological status of natural surface water, in terms of dominant trace metals, within an area subject to various sources of pollution including a non-ferrous metal ore mining, such as the West Rhodope Mountain, Bulgaria, is significant. The present study estimates the ecological status of river body waters at industrial areas of the West Rhodope Mountain, Bulgaria, simultaneously evaluating the possibility of state forecasting, together with assessing the potential risks, through the study of scenarios focusing on (i) possible variations of physicochemical parameters such as pH, concentration levels of trace metals, sulphates, and dissolved organic carbon (DOC) of surface water and (ii) consideration of potential spontaneous precipitation reactions in the studied waters. The ecological status of river body waters was assessed through a combination of experimental field, laboratory, and computational techniques. Al, Mn, Zn, and Pb were found to be the dominant pollutants with a variety of chemical species and distribution. The most significant difference characterizing the chemical species distribution in light of total spontaneous crystallization in the systems was found for Pb, followed by Zn and Mn, with the differences being more significant at lower trace metal levels. The calculated species were discussed on the basis of HSAB (hard and soft acids and bases) principle.

This study is a wide-ranging evaluation of groundwater within the calcareous semiarid area, Gaziantep in southeast Anatolia, Turkey. The resulting water chemistry data (1) explains the interactions between rock and water, (2) evaluates the quantitative relationships between chemical species (major ions), (3) separates hydrochemical facies, (4) provides information on current water quality for multiple uses, and (5) acts as a benchmark for future research. Relationships between ion concentrations (as meq/L) were analyzed through linear modeling and calculation of coefficients of determination ( R 2 ). Stoichiometric calculations were employed to determine the quantitative relationships between ions in groundwater. Calculations between (Ca 2+ +Mg 2+ ) and HCO 3 − indicated that, even at different concentrations of the total alkaline earth metal ion (M 2+ ), the relative percent remained at 72% for all samples. The majority of Ca 2+ , Mg 2+ , and HCO 3 − ions in groundwater were derived from weathering of calcite, the most common mineral in the local geology. Weathering of dolomite was also important to the contribution of ions in some areas. Ca-HCO 3 was found to be the dominant water type for 81% of raw samples; a mixed water type was found in 17% of the samples. The major dissolved components of groundwater are, therefore, Ca(HCO 3 ) 2 and, to a lesser degree, Mg(HCO 3 ) 2 . The sampled groundwater was generally found to meet drinking water quality guidelines for most of the physicochemical quality properties for which standards are available, and with regard to concentrations of Mg 2+ , Na + , K + , Cl − , SO 4 2− , NO 2 − , and NH 4 + . However, NO 3 − , Ca 2+ , and HCO 3 − concentrations in several groundwater samples were in excess of maximum acceptable concentrations (MACs).

Plants being sessile organisms are often exposed to various abiotic stress conditions, which greatly hamper the growth, yields as well as the quality of produce. Plants respond to abiotic stresses in an exceptionally complex and coordinated manner, involving the interactions and crosstalk with many metabolic-molecular pathways. One of the most common responses is generation of reactive chemical species including reactive oxygen species (ROS), reactive nitrogen species (RNS), reactive carbonyl species (RCS) and reactive sulfur species (RSS). ROS and RNS have long attracted attention from the plant researchers for both their damaging as well as protective effects. However, several reports are emerging to confirm similar roles played by the relatively newer 'reactive' members, the RCS and RSS. Plant reactive species are also hailed as vivacious signaling molecules that play regulatory roles in many plant metabolic procedures. Undeniably, these reactive species are involved in virtually all aspects of plant cell functions. Reactive species and the antioxidant machinery maintain a delicate but critical cellular redox-balance which gets disturbed under stress conditions, where their biosynthesis, transportation, scavenging and the overall metabolism gets decisive for plant survival. The current review aims to highlight and discuss the role of ROS, RNS, RCS, and RSS in plants especially under abiotic stresses, cross-talks between them, current approaches and technological advents for their characterization, and a perspective view on exploration/manipulation of the pathways and check-points involved in biosynthesis, transport and scavenging of these reactive species for engineering abiotic stress tolerant crop plants.

A robust and efficient extraction method was developed to detect a broad range of pollutants of emerging interest in three freshwater invasive species: American red crab (Prokambarus clarkii), Asian clam (Corbicula fluminea), and pumpkinseed fish (Lepomis gibbosus). One native species, \"petxinot\" clam (Anodonta cygnea), was also evaluated. Invasive species are often more resistant to contamination and could be used in biomonitoring studies to assess the effect of contaminants of emerging concern on aquatic ecosystems while preserving potentially threatened native species. So far, most extraction methods developed for this purpose have focused on analyzing fish and generally focus on a limited number of compounds, especially analyzing compounds from the same family. In this sense, we set out to optimize a method that would allow the simultaneous extraction of 87 PhACs, 11 flame retardants, 21 per- and poly-fluoroalkyl substances, and 54 pesticides. The optimized method is based on ultrasound-assisted solvent extraction. Two tests were performed during method development, one to choose the extraction solvent with the best recovery efficiencies and one to select the best clean-up. The analysis was performed by high-performance liquid chromatography coupled to high-resolution mass spectrometry. The method obtained recoveries between 40 and 120% and relative standard deviations of less than 25% for 85% of the analytes in the four validated matrices. Limits of quantification between 0.01 ng g−1 and 22 ng g−1 were obtained. Application of the method on real samples from the Albufera Natural Park of Valencia (Spain) confirmed the presence of contaminants of emerging concern in all samples, such as acetaminophen, hydrochlorothiazide, tramadol, PFOS, carbendazim, and fenthion. PFAS were the group of compounds with the highest mean concentrations. C. fluminea was the species with the highest detection frequency, and P. clarkii had the highest average concentrations, so its use is prioritized for biomonitoring studies.

Trace metals pollution of surface waters and their nearby soils in the metallurgically polluted Kardjali region, Bulgaria, were studied. Thermodynamic modeling including the dissolved organic carbon (DOC) was carried out for evaluating the distribution of metal species in waters and soil solutions. Zn was found to be the most widespread pollutant in the water samples, followed by Cu, Mn, and Cd. Geoaccumulation indices of trace metals for the tested soils were calculated, indicating that regarding Al, Fe, Co, Ni, and Cu all soils are “uncontaminated”. The most significant soil pollutant was found to be Cd, with all soils being either “extremely contaminated” by this metal or close to the limit, followed by Pb and Zn. The dynamics of trace metal chemical species distribution in surface waters and in the water-soluble soil fractions, as a result of possible spontaneous precipitations, was calculated by applying different thermodynamic models. Regarding Mn, Co, Ni, and Cd in waters and aqueous soil extracts and Zn in aqueous soil extracts, their free ion species prevailed, being more labile and hence toxic for the ecosystem. In the case of Al, Fe, Cu, Cd, and Pb in the waters and aqueous soil extracts and of Zn in waters, stable organic complexes with bidentate bonds, Me(OH) 4 − or Me(OH) 0 2 prevailed.

Reactive oxygen species (ROS) are reactive compounds derived from oxygen. In biological systems, an excessive amount of ROS can cause oxidative damage to biological macromolecules being involved in different diseases. Several assays have been developed in the last 30 years for ROS evaluation. The objective of this article will be to provide an update about the spectrophotometric methods currently used in the assessment of ROS in serum. The chemical basis of four different techniques will be reviewed, and examples of their possible applications will be provided. A particular emphasis about the practical applications of these assays in the dog will be made, but selected information about their use in humans will also be presented for comparative purposes, following a One-Health approach. The information about the spectrophotometric assays presented in this paper should be interpreted with caution once limited information about them is available yet, and further studies should be performed to clarify what they measure and their clinical application. Ideally, when applied to evaluate a sample’s oxidative status, they should be incorporated in a panel of analytes where other oxidants, antioxidants, and biomarkers of inflammation were also included.

The use of saliva as a biological sample has many advantages, being especially relevant in pigs where the blood collection is highly stressful and painful, both for the animal and the staff in charge of the sampling. Currently one of the main uses of saliva is for diagnosis and detection of infectious diseases, but the saliva can also be used to measure biomarkers that can provide information of stress, inflammation, immune response and redox homeostasis. This review will be focused on the analytes that can be used for such evaluations. Emphasis will be given in providing data of practical use about their physiological basis, how they can be measured, and their interpretation. In addition, some general rules regarding sampling and saliva storage are provided and the concept of sialochemistry will be addressed. There is still a need for more data and knowledge for most of these biomarkers to optimize their use, application, and interpretation. However, this review provides updated data to illustrate that besides the detection of pathogens in saliva, additional interesting applicative information regarding pigs´ welfare and health can be obtained from this fluid. Information that can potentially be applied to other animal species as well as to humans.

The deployment of metal–organic frameworks (MOFs) in a plethora of analytical and bioanalytical applications is a growing research area. Their unique properties such as high but tunable porosity, well-defined channels or pores, and ease of post-synthetic modification to incorporate additional functional units make them ideal candidates for sensing applications. This is possible because the interaction of analytes with a MOF often results in a change in its structure, eventually leading to a modification of the intrinsic physicochemical properties of the MOF which is then transduced into a measurable signal. The high porosity allows for the adsorption of analytes very efficiently, while the tunable pore sizes/nature and/or installation of specific recognition groups allow modulating the affinity towards different classes of compounds, which in turn lead to good sensor sensitivity and selectivity, respectively. Some figures are given to illustrate the potential of MOF-based sensors in the most relevant application fields, and future challenges and opportunities to their possible translation from academia (i.e., laboratory testing of MOF sensing properties) to industry (i.e., real-world analytical sensor devices) are critically discussed. Graphical abstract

The Eastern Mediterranean Sea (EMS) is oligotrophic, presenting low biological production and high temperature and salinity, while comprising a biodiversity hotspot, with a unique emblematic threatened species array, including sea turtles. The establishment of healthy captive green turtle ( Chelonia mydas ) baseline blood analyte reference intervals (RIs) will contribute to improving diagnosis, treatment, rehabilitation and conservation success rates for sea turtles, by offering information with therapeutic and prognostic implications. However, baseline plasma chemistry and hematological analytes of EMS C. mydas are still unavailable. Hence, this study aimed to establish RIs for several blood analytes in general and under different life and rehabilitation stages and compare results with congeneric and conspecifics of other regions: Mediterranean loggerhead turtles ( Caretta caretta ) and two Atlantic green turtle populations. The study engulfed 118 blood samples obtained from 72 turtles admitted to the Israel Sea Turtle Rescue Centre between 2008 and 2020. Blood analyses included plasma chemistry and packed cell volume (PCV), and their association with body size and health status, and enabled suggesting RIs for PCV, plasma glucose and potassium concentrations, and aspartate transaminase and alkaline phosphatase activities. The PCV were significantly associated with rehabilitation. Noted differences arising via population comparison are likely associated with interspecific dietary and metabolic traits. These novel physiological results form the basis for future studies, and provide caregivers a tool potentially increasing the success of recovery, rehabilitation and conservation efforts. Further research is warranted to fill knowledge gaps concerning physiology and potential ecological impacts on this species.

Levels and chemical species of reactive oxygen/nitrogen species (ROS/RNS) determine oxidative eustress and distress. Abundance of uptake pathways and high oxygen consumption for ATP-dependent transport makes the renal proximal tubule particularly susceptible to cadmium (Cd2+)-induced oxidative stress by targeting ROS/RNS generation or antioxidant defence mechanisms, such as superoxide dismutase (SOD) or H2O2-metabolizing catalase (CAT). Though ROS/RNS are well-evidenced, the role of distinct ROS profiles in Cd2+ concentration-dependent toxicity is not clear. In renal cells, Cd2+ (10–50 µM) oxidized dihydrorhodamine 123, reaching a maximum at 2–3 h. Increases (up to fourfold) in lipid peroxidation by TBARS assay and H2O2 by Amplex Red were evident within 30 min. ROS and loss in cell viability by MTT assay with 50 µM Cd2+ could not be fully reversed by SOD mimetics Tempol and MnTBAP nor by SOD1 overexpression, whereas CAT expression and α-tocopherol were effective. SOD and CAT activities were attenuated below controls only with >6 h 50 µM Cd2+, yet augmented by up to 1.5- and 1.2-fold, respectively, by 10 µM Cd2+. Moreover, 10 µM, but not 25–50 µM Cd2+, caused 1.7-fold increase in superoxide anion (O2•−), detected by dihydroethidium, paralled by loss in cell viability, that was abolished by Tempol, MnTBAP, α-tocopherol and SOD1 or CAT overexpression. H2O2-generating NADPH oxidase 4 (NOX4) was attenuated by ~50% with 10 µM Cd2+ at 3 h compared to upregulation by 50 µM Cd2+ (~1.4-fold, 30 min), which was sustained for 24 h. In summary, O2•− predominates with low–moderate Cd2+, driving an adaptive response, whereas oxidative stress by elevated H2O2 at high Cd2+ triggers cell death signaling pathways.HighlightsDifferent levels of reactive oxygen species are generated, depending on cadmium concentration.Superoxide anion predominates and H2O2 is suppressed with low cadmium representing oxidative eustress.High cadmium fosters H2O2 by inhibiting catalase and increasing NOX4 leading to oxidative distress.Superoxide dismutase mimetics and overexpression were less effective with high versus low cadmium.Oxidative stress profile could dictate downstream signalling pathways.