Environmental Compartments Research Articles

Embryotoxicity Induced by Triclopyr in Zebrafish (Danio rerio) Early Life Stage.

Triclopyr, an auxin-like herbicide that is widely employed for managing weeds in food crops and pastures, has been identified in various environmental settings, particularly aquatic ecosystems. Limited understanding of the environmental fate of this herbicide, its potential repercussions for both the environment and human health, and its insufficient monitoring in diverse environmental compartments has caused it to be recognized as an emerging contaminant of concern. In this study, we have investigated how triclopyr affects zebrafish, considering a new alternative methodology. We focused on the endpoints of developmental toxicity, neurotoxicity, and behavior of zebrafish embryos and larvae. We determined that triclopyr has a 96 h median lethal concentration of 87.46 mg/L (341.01 µM). When we exposed zebrafish embryos to sublethal triclopyr concentrations (0.5, 1, 5, 10, and 50 μM) for up to 144 h, we found that 50 µM triclopyr delayed zebrafish egg hatchability. Yolk sac malabsorption was significant at 0.5, 1, 5, and 10 µM triclopyr. In zebrafish larvae, uninflated swim bladder was significant only at 50 µM triclopyr. Furthermore, zebrafish larvae had altered swimming activity after exposure to 10 µM triclopyr for 144 h. In summary, these comprehensive results indicate that even low triclopyr concentrations can elicit adverse effects during early zebrafish development.

Assessment of Heavy Metal on Nasipit Port

This study aimed to assess the presence of heavy metals, specifically Cadmium (Cd), Copper (Cu), Lead (Pb), Magnesium (Mg), Nickel (Ni), and Silver (Ag), in Nasipit Port, Nasipit, Agusan Del Norte, Philippines. The study measured and quantified the concentrations of these heavy metals in various environmental compartments within and around the port area, including water and sediment samples. This study employed an experimental research design to investigate the presence of heavy metals in Nasipit Port. The research utilized DOST's laboratory equipment and did not involve human respondents. The sampling method involved measuring the distance from the ship to collect water and sediment samples. The study ensured informed consent, voluntary participation, and privacy protection for the participants. The results showed that Cadmium, Copper, Lead, and Nickel were not detected, while Magnesium and Silver exceeded the standard limits set by the DENR. The study found no significant difference in heavy metal contamination between areas with and without ships, indicating that the port is still classified as safe for ecological risk assessment. The recommendations emphasize the importance of community engagement, continuous monitoring, and public awareness to protect the marine ecosystem and public health. Finally, future researchers are encouraged to expand the study to include other heavy metals and investigate their bioaccumulation in fish and other marine organisms.

Comprehensive assessment of exposure and environmental risk of potentially toxic elements in surface water and sediment across China: A synthesis study

China faces a serious challenge with water pollution posed by potentially toxic elements (PTEs). Comprehensive and reliable environmental risk assessment is paramount for precise pollution prevention and control. Previous studies generally focused on a single environmental compartment within small regions, and the uncertainty in risk calculation is not fully considered. This study revealed the current exposure status of 11 PTEs in surface water and sediment across China using previously reported concentration data in 301 well-screened articles. Ecological and human health risks were evaluated and the uncertainty related to calculation parameters and exposure dataset were quantified. PTEs of high concern were further identified. Results showed Mn and Zn had the highest concentration levels, while Hg and Cd had the lowest concentrations in both surface water and sediment. Risk assessment of individual PTE showed that high-risk PTEs varied by risk receptors and environmental compartments. Nationwide, the probability of aquatic organisms being affected by Mn, Zn, Cu, and As in surface water exceeded 10 %. In sediment, Cd and Hg exhibited high and considerable risk, respectively. As was identified as the major PTE threatening human health as its carcinogenic risk was 1.45 × 10−4 through direct ingestion. Combined risk assessment showed the PTE mixture in surface water and sediment posed medium and high ecological risk with the risk quotient and potential ecological risk index of 1.76 and 558.36, respectively. Adverse health effects through incidental ingestion and dermal contact during swimming were negligible. This study provides a nationwide risk assessment of PTEs in China's aquatic environment and the robustness is verified, which can serve as a practical basis for policymakers to guide the early warning and precise management of water pollution.

How many microplastics do you need to (sub)sample?

Analysis of microplastics in the environment requires polymer characterization as a confirmation step for suspected microplastic particles found in a sample. Material characterization is costly and can take a long time per particle. When microplastic particle counts are high, many researchers cannot characterize every particle in their sample due to time or monetary constraints. Moreover, characterizing every particle in samples with high plastic particle counts is unnecessary for describing the sample properties. We propose an a priori approach to determine the number of suspected microplastic particles in a sample that should be randomly subsampled for characterization to accurately assess the polymer distribution in the environmental sample. The proposed equation is well-founded in statistics literature and was validated using published microplastic data and simulations for typical microplastic subsampling routines. We report values from the whole equation but also derive a simple way to calculate the necessary particle count for samples or subsamples by taking the error to the power of negative two. Assuming an error of 0.05 (5 %) with a confidence interval of 95 %, an unknown expected proportion, and a sample with many particles (> 100k), the minimum number of particles in a subsample should be 386 particles to accurately characterize the polymer distribution of the sample, given the particles are randomly characterized from the full population of suspected particles. Extending this equation to simultaneously estimate polymer, color, size, and morphology distributions reveals more particles (620) would be needed in the subsample to achieve the same high absolute error threshold for all properties. The above proposal for minimum subsample size also applies to the minimum count that should be present in samples to accurately characterize particle type presence and diversity in a given environmental compartment.

Fragmentation Pattern-Based Screening Strategy Combining Diagnostic Ion and Neutral Loss Uncovered Novel para-Phenylenediamine Quinone Contaminants in the Environment.

Identifying transformed emerging contaminants in complex environmental compartments is a challenging but meaningful task. Substituted para-phenylenediamine quinones (PPD-quinones) are emerging contaminants originating from rubber antioxidants and have been proven to be toxic to the aquatic species, especially salmonids. The emergence of multiple PPD-quinones in various environmental matrices and evidence of their specific hazards underscore the need to understand their environmental occurrences. Here, we introduce a fragmentation pattern-based nontargeted screening strategy combining full MS/All ion fragmentation/neutral loss-ddMS2 scans to identify potential unknown PPD-quinones in different environmental matrices. Using diagnostic fragments of m/z 170.0600, 139.0502, and characteristic neutral losses of 199.0633, 138.0429 Da, six known and three novel PPD-quinones were recognized in air particulates, surface soil, and tire tissue. Their specific structures were confirmed, and their environmental concentration and composition profiles were clarified with self-synthesized standards. N-(1-methylheptyl)-N'-phenyl-1,4-benzenediamine quinone (8PPD-Q) and N,N'-di(1,3-dimethylbutyl)-p-phenylenediamine quinone (66PD-Q) were identified and quantified for the first time, with their median concentrations found to be 0.02-0.21 μg·g-1 in tire tissue, 0.40-2.76 pg·m-3 in air particles, and 0.23-1.02 ng·g-1 in surface soil. This work provides new evidence for the presence of unknown PPD-quinones in the environment, showcasing a potential strategy for screening emerging transformed contaminants in the environment.

Meteorological, snow and soil data, CO2, water and energy fluxes from a low-Arctic valley of Northern Quebec

Abstract. As the vegetation in the Arctic changes, tundra ecosystems along the southern border of the Arctic are becoming greener and gradually giving way to boreal ecosystems. This change is affecting local populations, wildlife, energy exchange processes between environmental compartments, and the carbon cycle. To understand the progression and the implications of this change in vegetation, satellite measurements and surface models can be employed. However, in situ observational data are required to validate these measurements and models. This paper presents observational data from two nearby sites in the forest–tundra ecotone in the Tasiapik Valley near Umiujaq in Northern Quebec, Canada. One site is on a mixture of lichen and shrub tundra. The associated data set comprises 9 years of meteorological, soil and snow data as well as 3 years of eddy covariance data. The other site, 850 m away, features vegetation consisting mostly of tall shrubs and black spruce. For that location, 6 years of meteorological, soil and snow data are available. In addition to the data from the automated stations, profiles of snow density and specific surface area were collected during field campaigns. The data are available at https://doi.org/10.1594/PANGAEA.964743 (Domine et al., 2024).

Interactions shape aquatic microbiome responses to Cu and Au nanoparticle treatments in wetland manipulation experiments

In natural systems, organisms are embedded in complex networks where their physiology and community composition is shaped by both biotic and abiotic factors. Therefore, to assess the ecosystem-level effects of contaminants, we must pair complex, multi-trophic field studies with more targeted hypothesis-driven approaches to explore specific actors and mechanisms. Here, we examine aquatic microbiome responses to long-term additions of commercially-available metallic nanoparticles [copper-based (CuNPs) or gold (AuNPs)] and/or nutrients in complex, wetland mesocosms over 9 months, allowing for a full growth cycle of the aquatic plants. We found that both CuNPs and AuNPs (but not nutrient) treatments showed shifts in microbial communities and populations largely at the end of the experiment, as the aquatic plant community senesced. we examine aquatic microbiomes under chronic dosing of NPs and nutrients Simplified microbe-only or microbe + plant incubations revealed that direct effects of AuNPs on aquatic microbiomes can be buffered by plants (regardless of seasonal As mesocosms were dosed weekly, the absence of water column accumulation indicates the partitioning of both metals into other environmental compartments, mainly the floc and aquatic plants photosynthetically-derived organic matter. Overall, this study identifies the potential for NP environmental impacts to be either suppressed by or propagated across trophic levels via the presence of primary producers, highlighting the importance of organismal interactions in mediating emerging contaminants’ ecosystem-wide impacts.

Per- and Polyfluoroalkyl Substances in Water (2008-2022) and Fish (2015-2022) in The Netherlands: Spatiotemporal Trends, Fingerprints, Mass Discharges, Sources, and Bioaccumulation Factors.

Per- and polyfluoroalkyl substances (PFAS) are persistent, bioaccumulative, and toxic synthetic chemicals of concern, which have been detected in nearly all environmental compartments. The present study provides a data analysis on PFAS concentrations in the Dutch inland and coastal national waters and fish sampled from 2008 to 2022 and 2015 to 2022, respectively. Although the fish database is relatively small, the water database is unique because of its temporal dimension. It appears that PFAS are omnipresent in Dutch water and fish, with relatively small spatial differences in absolute and relative concentrations (fingerprints) and few obvious temporal trends. Only perfluorooctanoic acid and perfluorooctanesulfonic acid (PFOS) aqueous concentrations in the rivers Rhine and Scheldt have substantially decreased since 2012. Still, PFOS concentrations exceed the European water quality standards at all and fish standards at many locations. Masses of PFAS entering the country and the North Sea are roughly 3.5 tonnes/year. Generally, the data suggest that most PFAS enter the Dutch aquatic environment predominantly through diffuse sources, yet several major point sources of specific PFAS were identified using fingerprints and monthly concentration profiles as identification tools. Finally, combining concentrations in fish and water, 265 bioaccumulation factors were derived, showing no statistically significant differences between freshwater and marine fish. Overall, the analysis provides new insights into PFAS bioaccumulation and spatiotemporal trends, mass discharges, and sources in The Netherlands. Environ Toxicol Chem 2024;43:965-975. © 2024 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.

Preliminary insights on the development of a continuous-flow solar system for the photocatalytic degradation of contaminants of emerging concern in water.

The ubiquity and impact of pharmaceuticals and pesticides, as well as their residues in environmental compartments, particularly in water, have raised human and environmental health concerns. This emphasizes the need of developing sustainable methods for their removal. Solar-driven photocatalytic degradation has emerged as a promising approach for the chemical decontamination of water, sparking intensive scientific research in this field. Advancements in photocatalytic materials have driven the need for solar reactors that efficiently integrate photocatalysts for real-world water treatment. This study reports preliminary results from the development and evaluation of a solar system for TiO2-based photocatalytic degradation of intermittently flowing water contaminated with doxycycline (DXC), sulfamethoxazole (SMX), dexamethasone (DXM), and carbendazim (CBZ). The system consisted of a Fresnel-type UV solar concentrator that focused on the opening and focal point of a parabolic trough concentrator, within which tubular quartz glass reactors were fixed. Concentric springs coated with TiO2, arranged one inside the other, were fixed inside the quartz reactors. The reactors are connected to a raw water tank at the inlet and a check valve at the outlet. Rotating wheels at the collector base enable solar tracking in two axes. The substances (SMX, DXC, and CBZ) were dissolved in dechlorinated tap water at a concentration of 1.0mg/L, except DXM (0.8mg/L). The water underwent sequential batch (~ 3 L each, without recirculation) processing with retention times of 15, 30, 60, 90, and 120min. After 15min, the degradation rates were as follows: DXC 87%, SMX 35.5%, DXM 32%, and CBZ 31.8%. The system processed 101 L of water daily, simultaneously removing 870, 355, 256, and 318µg/L of DXC, SMX, DXM, and CBZ, respectively, showcasing its potential for real-world chemical water decontamination application. Further enhancements that enable continuous-flow operation and integrate highly effective adsorbents and photocatalytic materials can significantly enhance system performance.

Tracking the transformation of persistent organic pollutants in food webs using multi element isotope and enantiomer fractionation

In order to track the transformation of persistent organic pollutants (POPs) in food webs, field experiments were conducted at two sites using stable isotope and enantiomer fractionation concepts. The enantiomers of α-hexachlorocyclohexane (α-HCH) were selected as representative compounds for POPs. Isotope and enantiomer fractionation allowed the characterization of α-HCH enantiomer biotransformation processes along trophic levels of the food web - from soil and plants to animal livers, fat tissues and milk. The enrichment of heavy isotopes in soils, plants and sediments as well as the changes of enantiomer fractionation indicate that the biotransformation of α-HCH occurred in these compartments. Moreover, the increase of carbon and chlorine isotopic compositions as well as the changes of enantiomer fractionation of liver, fat tissues and milk demonstrated that the overall HCH exposure was much higher than estimates based on concentration levels, while the isotope and enantiomer fractionation revealed the enantiomer specific enantiomer uptake across the blood-brain barriers. Dual element isotope analysis suggested that complex transformation processes have occurred along the potential food web from the HCH sources over different environmental compartments to animal livers, fat tissues and milk. The results imply that the analyses of stable isotope compositions and concentrations has potential to reconstruct the exposure of higher organisms to POPs.

Application of electron beam technology to decompose per- and polyfluoroalkyl substances in water

The widespread detection of per- and polyfluoroalkyl substances (PFAS) in environmental compartments across the globe has raised several health concerns. Destructive technologies that aim to transform these recalcitrant PFAS into less toxic, more manageable products, are gaining impetus to address this problem. In this study, a 9 MeV electron beam accelerator was utilized to treat a suite of PFAS (perfluoroalkyl carboxylates: PFCAs, perfluoroalkyl sulfonates, and 6:2 fluorotelomer sulfonate: FTS) at environmentally relevant levels in water under different operating and water quality conditions. Although perfluorooctanoic acid and perfluorooctane sulfonic acid showed >90% degradation at <500 kGy dose at optimized conditions, a fluoride mass balance revealed that complete defluorination occurred only at/or near 1000 kGy. Non-target and suspect screening revealed additional degradation pathways differing from previously reported mechanisms. Treatment of PFAS mixtures in deionized water and groundwater matrices showed that FTS was preferentially degraded (∼90%), followed by partial degradation of long-chain PFAS (∼15–60%) and a simultaneous increase of short-chain PFAS (up to 20%) with increasing doses. The increase was much higher (up to 3.5X) in groundwaters compared to deionized water due to the presence of PFAS precursors as confirmed by total oxidizable precursor (TOP) assay. TOP assay of e-beam treated samples did not show any increase in PFCAs, confirming that e-beam was effective in also degrading precursors. This study provides an improved understanding of the mechanism of PFAS degradation and revealed that short-chain PFAS are more resistant to defluorination and their levels and regulation in the environment will determine the operating conditions of e-beam and other PFAS treatment technologies.

Emerging organic contaminants in the soil-plant-receptor continuum: transport, fate, health risks, and removal mechanisms.

There is a lack of comprehensive reviews tracking emerging organic contaminants (EOCs) within the soil-plant continuum using the source-pathway-receptor-impact-mitigation (SPRIM) framework. Therefore, this review examines existing literature to gain insights into the occurrence, behaviour, fate, health hazards, and strategies for mitigating EOCs within the soil-plant system. EOCs identified in the soil-plant system encompass endocrine-disrupting chemicals, surfactants, pharmaceuticals, personal care products, plasticizers, gasoline additives, flame retardants, and per- and poly-fluoroalkyl substances (PFAS). Sources of EOCs in the soil-plant system include the land application of biosolids, wastewater, and solid wastes rich in EOCs. However, less-studied sources encompass plastics and atmospheric deposition. EOCs are transported from their sources to the soil-plant system and other receptors through human activities, wind-driven processes, and hydrological pathways. The behaviour, persistence, and fate of EOCs within the soil-plant system are discussed, including sorption, degradation, phase partitioning, (bio)transformation, biouptake, translocation, and bioaccumulation in plants. Factors governing the behaviour, persistence, and fate of EOCs in the soil-plant system include pH, redox potential, texture, temperature, and soil organic matter content. The review also discusses the environmental receptors of EOCs, including their exchange with other environmental compartments (aquatic and atmospheric), and interactions with soil organisms. The ecological health risks, human exposure via inhalation of particulate matter and consumption of contaminated food, and hazards associated with various EOCs in the soil-plant system are discussed. Various mitigation measures including removal technologies of EOCs in the soil are discussed. Finally, future research directions are presented.

Assessment of anthropogenic particles content in commercial beverages

Microplastic (MPs) pollution is a current global concern that is affecting all environmental compartments and food sources. In this work, anthropogenic particles occurrence (MPs and natural and synthetic cellulosic particles), have been determined in 73 beverages packed in different containers. Overall, 1521 anthropogenic particles were found, being the lowest occurrence in water samples (7.2 ± 10.1 items·L−1) while beer had the highest (95.5 ± 91.8 items·L−1). Colourless/white particles were the most detected followed by blue and red colours. The highest mean size was 783 ± 715 μm in soft drinks. Cellulosic, both natural and semisynthetic particles, were the composition mostly found but regarding plastic polymers, it was polyester. Phenoxy resin particles from the can coatings were also identified in all metal containers which indicates that leaching from the packaging may be happening. The total estimated daily intake were 0.077 and 0.159 items·kg−1 body weight (b.w.)·day−1 for children and adult population, respectively.

Remediation of imidacloprid and carbamazepine in polluted soil using TiO2 with LED lamps

Imidacloprid and carbamazepine are recognised as emerging contaminants (ECs) due to their ubiquitous presence in environmental compartments and their potential to cause undesirable ecological effects. Wastewater treatment plants are relevant routes for these compounds to enter environment since they are continuously released through treated wastewater. The progressively more extended custom of reusing treated wastewater for agricultural irrigation has also enlarged the risks for ECs accumulation in soil and their translocation to crops, posing a constant threat to both humans and wildlife. This work is aimed to study the behaviour of imidacloprid and carbamazepine and its main transformation products generated in soil during photocatalytic treatments using commercial TiO2 (Degussa P25) and ultraviolet light emitting diode (UV-LED) lamps as light source. Prior to remediation trial, the influence of catalyst load and soil moisture content in ECs degradation was studied. Experiments were performed using a photochemical reactor equipped with LED lamps running at 365 nm, exposing polluted soils to different treatments in presence and absence of photocatalyst. A significant degradation (93.4 and 96.2% for imidacloprid and carbamazepine, respectively) was observed after 4 days of photocatalytic treatment. The main transformation products were identified during the different treatments. Our results suggest that TiO2-photocatalytic treatment combined with UV-LED could be considered a promising technology to remove ECs from soils.

Reuse of polymeric waste for the treatment of marine water polluted by diesel

Accidental diesel spills can occur in marine environments such as harbors, leading to adverse effects on the environmental compartment and humans. This study proposes the surgical mask as an affordable and sustainable adsorbent for the remediation of diesel–contaminated seawater to cope with the polymeric waste generated monthly in hospital facilities. This approach can also be helpful considering a possible future pandemic, alleviating the pressure on the waste management system by avoiding improper mask incineration and landfilling, as instead occurred during the previous COVID–19. Batch adsorption–desorption experiments revealed a complete diesel removal from seawater after 120 min with the intact laceless mask, which showed an adsorption capacity of up to 3.43 g/g. The adsorption curve was better predicted via Weber and Morris's kinetic (R2 = 0.876) and, in general, with Temkin isotherm (R2 = 0.965–0.996) probably due to the occurrence of chemisorption with intraparticle diffusion as one of the rates–determining steps. A hysteresis index of 0.23–0.36 was obtained from the desorption isotherms, suggesting that diesel adsorption onto surgical masks was faster than the desorption mechanism. Also, the effect of pH, ionic strength and temperature on diesel adsorption was examined. The results from the reusability tests indicated that the surgical mask can be regenerated for 5 consecutive cycles while decreasing the adsorption capacity by only approximately 11%.

Elementary flow mapping across life cycle inventory data systems: A case study for data interoperability under the Global Life Cycle Assessment Data Access (GLAD) initiative

PurposeLimited availability of life cycle assessment (LCA) data poses a significant challenge to its mainstream adoption, rendering it a central issue within the LCA community. The Global LCA Data Access (GLAD) network aims to increase the accessibility and interoperability of LCA data and offers benefits for different use cases. GLAD is an intergovernmental collaboration involving different stakeholders organized into working groups. The GLAD Nomenclature Working Group (NWG) developed a procedure and a set of criteria to map elementary flows among major nomenclature systems and reviewed bidirectional mappings. This paper provides an overview of the methodological approach followed by the NWG to achieve the resulting mapping files.MethodsThe mapping procedure involves several steps of flow and compartment matches and bilateral review. The procedure is supported by an ad hoc software tool called the “GLAD Mapper Tool” developed with the NWG and which is made available for free by the European Commission. The input files for the procedure are the properly formatted source and target flow lists and a file containing the mapping criteria. The four nomenclature systems mapped are those used in ecoinvent, Environmental Footprint, IDEA, and the U.S. Federal LCA Commons. The procedure included representatives from each of these nomenclature systems to ensure a multilateral agreement on the approach to verifying and assessing the quality of the results. The iterative mapping process included different stages of bidirectional reviews to achieve a balance between mapping coverage (i.e., percentage of source flows covered by the target list) and accuracy.Results and discussionThe mapping procedure proved to be an efficient approach for LCA practitioners in mappings between different nomenclature systems. After a relatively low number of iterations, mapping coverages higher than 90% were achieved, which is driven by the availability of unique substances (flow names) and the granularity of environmental compartments. Overall, none of the four flow lists achieved full coverage and the use of approximated matches (proxy matches) for environmental compartments and/or substances was necessary when a perfect matches between flows were not possible.ConclusionsThe NWG’s mapping activities may serve as a starting point towards defining a central hub for mapping impact assessment methods and datasets, improving data accessibility and interoperability for the LCA community as a step towards defining a unified nomenclature system. The GLAD mapping approach is open and transparent. The approach fosters traceability in the mapping process and offers the potential for greater interoperability across the LCA community, underlining the commitment to openness and collaboration.

A narrative review of microplastics in the indoor and outdoor environment, human effects, and ecological risks

Due to their widespread identification in all environmental compartments, Microplastics (MPs) are emerging pollutants that have garnered growing scientific and public attention over the last decades. Early research on MPs and their effects was limited to studies of terrestrial and aquatic ecosystems, but more recent studies have included MPs in the air. There is now considerable concern about the effects of MPs on pristine environments and urban air quality.&#x0D; A literature search was conducted in Science Direct and Google Scholar using the following keywords: microplastics, indoor environment, outdoor environment, human effects, and ecological risks.&#x0D; Finally, eligible studies were selected for the review. Textiles, such as clothes, carpets, and curtains, are the main indoor sources of MPs. As well as the primary sources of MPs outdoors, there are landfills, urban and home dust, and synthetic particles. According to current theories, human exposure to MPs occurs through dermal contact, ingestion, and inhalation. Recent research has demonstrated that inhalation is the principal mechanism of human exposure to MPs. Early toxicological research suggests that MPs may lead to inflammation and oxidative stress. However, there is growing concern about the possible leaching of hazardous chemicals used as plastic additives. Nevertheless, MP exposure and risk assessment in humans is still in its infancy, and more research on the presence of MPs in various indoor and outdoor environments is required to provide the knowledge base needed for regulations to protect human health and the environment from MPs.

Ex-post impact assessment on a large environmental disaster

Impact assessments following environmental disasters must be quick and in accessible language so that decision-makers and affected populations are aware of the main impacts and can target recovery measures. After the collapse of the Fundão dam (Minas Gerais, Brazil) in November 2015, an extensive monitoring program was implemented to understand the aquatic environmental situation and associated biodiversity status after the spill of the iron ore tailings in a large and highly populated watershed, that reached the Atlantic Ocean along the southeast Brazilian coast. A monitoring programme faced several challenges, including the large volume of data to be analysed, which difficult an objective environmental diagnosis and the communication between technical teams and decision makers. In this context, an impact matrix was proposed as a tool for assessing the environmental proxy results and summarizing the results obtained. The proposed Impact Matrix is an interaction matrix adaptation which consists of quantifying the impacts using pre-defined criteria and scores. Expert panels assessed the link between environmental measures and objectives by scoring the specific criteria. As an interaction matrix, the impact matrix is made up of two intersecting axes: the identified impact and the affected environmental compartments (whether abiotic or biotic). The final impact matrix is reached by summing up the score for the criteria on each of the identified intersections. The impact matrix is a supervised approach focused on provide relatively simple tool to apply and, when carried out periodically in parallel with a monitoring programme, it makes it possible to observe temporal trends in the evolution of the environment after the event causing the impact. The impact matrix can also serve as feedback to the monitoring programme itself, when used in an adaptive management approach.

Overview of Per- and Polyfluoroalkyl Substances (PFAS), Their Applications, Sources, and Potential Impacts on Human Health

Per- and polyfluoroalkyl substances (PFAS) belong to a group of synthetic compounds that have recently raised concerns about human health and environmental quality due to their great prevalence, degradation resistance, and potential toxicity. This review focuses on the applications of PFAS and their effects on human health. Specific emphasis has been laid on (i) the application/use of PFAS, (ii) sources and distribution of PFAS in diverse environmental compartments, and (iii) the impact of PFAS on human health. Significant health effects on humans are associated with exposure to PFAS, i.e., immunotoxicity, thyroid and kidney disorders, cancer, etc. Conclusions obtained from PFAS studies demonstrate that inadequate evidence should not be used to justify delaying risk reduction steps for PFAS alternatives. PFAS can be determined in different environmental matrices using both traditional analytical approaches, i.e., liquid chromatography coupled with mass spectrometry (LC-MS/MS) and semi-quantitative and passive sampling, and advanced analytical methods with colorimetric, spectrofluorimetric, and electrochemical detection. Traditional methods are costly and not broadly available, while the emerging, cost-effective methods are less sensitive and unable to meet regulatory exposure limits. There is still a significant number of studies to be performed to fully comprehend the real contamination by PFAS.

Elucidating doxycycline biotransformation mechanism by Chryseobacterium sp. WX1: Multi-omics insights

Doxycycline (DOX) represents a second-generation tetracycline antibiotic that persists as a challenging-to-degrade contaminant in environmental compartments. Despite its ubiquity, scant literature exists on bacteria proficient in DOX degradation. This study marked a substantial advancement in this field by isolating Chryseobacterium sp. WX1 from an activated sludge enrichment culture, showcasing its unprecedented ability to completely degrade 50 mg/L of DOX within 44 h. Throughout the degradation process, seven biotransformation products were identified, revealing a complex pathway that began with the hydroxylation of DOX, followed by a series of transformations. Employing an integrated multi-omics approach alongside in vitro heterologous expression assays, our study distinctly identified the tetX gene as a critical facilitator of DOX hydroxylation. Proteomic analyses further pinpointed the enzymes postulated to mediate the downstream modifications of DOX hydroxylation derivatives. The elucidated degradation pathway encompassed several key biological processes, such as the microbial transmembrane transport of DOX and its intermediates, the orchestration of enzyme synthesis for transformation, energy metabolism, and other gene-regulated biological directives. This study provides the first insight into the adaptive biotransformation strategies of Chryseobacterium under DOX-induced stress, highlighting the potential applications of this strain to augment DOX removal in wastewater treatment systems containing high concentrations of DOX.