Organic Pollutants In Environment Research Articles

Portable and highly enhanced surface enhanced Raman scattering and photocatalytic activity of cost-effective hierarchical hollow metal organic frameworks heterostructures induced by etched titanium sheet

In order to effectively detect and remove organic toxics in wastewater, the facile construction of plug and play bifunctional materials is very vital. Herein, a kind of metal-organic frameworks (MIL-53 (Fe) with hollow tubular structure was induced by an etched Ti sheet (ET), and then small sized Ag nanoparticles (Ag NPs) were in-situ anchored evenly on the internal and external surfaces of MIL-53 (Fe). Subsequently, a new type of bifunctional material (ETMA) was assembled. Surface enhanced Raman scattering (SERS) and photocatalytic activity of the material were investigated with crystal violet (CV, a carcinogenic and teratogenic toxic) as an analyte. The results found that trace amount of CV (1 × 10−12 M) can still be sensitively detected by the fabricated ETMA, and analysis enhancement factors as high as 6.9 × 105 even though only 1.39 wt % Ag was contained in the ETMA. Moreover, nearly 100 % of CV can be rapidly degraded by the ETMA after irradiated for 15 min, which was 44.47 times and 7.27 times faster than those of ET-Ag (ETA) and ET-MIL-53 (Fe) (ETM), respectively. Additionally, the removal efficiency of total organic carbon (TOC) was as high as 75.44 %. The remarkable enrichment effect, the strong interaction among components, and the synergistic effect in the target ETMA material were responsible to the dramatically enhanced SERS and photocatalytic performances. In addition, the cost-effective ETMA exhibited excellent uniformity, repeatability, stability, and recyclability towards the detection and removal of CV in actual water samples, showing great potentials in monitoring and removing organic pollutants in practical ecological environment.

A novel nano-cerium oxide functionalized biochar composite for degradation of organic dye: insight of the photocatalysis mechanism.

Recently, visible-light-driven photocatalysis attracts much concerns in the remediation of environmental organic pollutants. In this study, the cerium doped biochar was fabricated through the hydrothermal method, and served as an efficient photocatalyst towards rhodamine B degradation under visible light irradiation. Almost 100% of rhodamine B was removed by 2.0g·L-1 cerium doped biochar after 60min of visible light irradiation at pH 3, but only about 25.50% and 29.60% of rhodamine B was removed by cerium dioxide and biochar under identical conditions. The degradation process coincided well with the pseudo-first-order kinetic model, and the photodegradation rate constant of cerium doped biochar was 0.0485·min-1, which was respectively 97 and 44 times that of biochar (0.0005·min-1) and cerium dioxide (0.0011·min-1). According to the trapping experiments and electron spin resonance spectroscopy analysis, h+, O2-∙ and ∙OH all participated in the degradation of rhodamine B in the cerium doped biochar photocatalytic systems, and the function of h+ and ∙OH was dominated. Consequently, the biochar could not only be an excellent carrier for supporting cerium dioxide, but also greatly improved its photocatalytic activity. The band gap of cerium doped biochar was narrower than cerium dioxide, which could improve the separation and migration of photogenerated electron-hole pairs under visible-light excitation, thus ultimately enhanced the degradation of rhodamine B. This work provided a deeper understanding of the preparation of biochar-based photocatalyst and its application in the remediation of environmental organic pollution.

Investigating oxidant-catalyst interactions in the persulfate system: Implications for efficient removal of phenolics and antibiotics

Persulfate (PS) activation by carbon catalyst holds both scientific and practical significance to curb the toxicity effects of organic pollutants in the natural water environment. Here, we investigated a relatively unfamiliar characteristics (i.e., oxidant-catalyst interaction) that influence the removal efficiency in PS activated system, utilizing N-doped mesoporous carbon hollow spheres (N-MCHS; size ∼385 nm) as a catalyst. The selection of this catalyst was motivated by its desired physicochemical characteristics such as high dispersibility, uniformly distributed pores and high specific surface area (1109 m2 g−1) for catalytic application. The removal performance was studied by degrading bisphenol A at very low PS (0.25 mM) and catalyst (10.0 mg L−1) concentrations. Through this study, we established a correlation between the surface charge of N-MCHS and PS interaction on the catalytic performance. Further, electron spin resonance (ESR) and radical scavenger studies were carryout out to prove the nonradical oxidation process. Electrochemical studies provided a strong evidence for PS complexation and electron transfer during oxidative removal of bisphenol A. Additional studies with different phenolics and antibiotics demonstrated that N-doping significantly accelerates the degradation rate and enhances the removal efficiency. The results of present study unveil the potential use of PS+N-MCHS in the degradation of different organic contaminants at low catalyst dosages.

Carbon based cobalt titanate perovskite nanocomposite: Synthesis, characterization, and excellent visible light driven photocatalytic performance

Titanium-based perovskite oxides are the promising photocatalysts for an efficient degradation of organic pollutants. However, charge carriers recombination and wide band gap energy are still the main challenges in their visible-light-driven photocatalytic applications of Titanate perovskites, ATiO3. The immobilization of Titanium-based perovskites on a carbonaceous substrate such as nitrogen-rich carbon nitride, can be considered as an excellent option for enhancing photocatalytic performance. Here, the CoTiO3/C3N5 nanocomposite was synthesized by simple reflux method and used for photocatalytic degradation of three organic pollutants including methylene blue (MB), tetracycline hydrochloride (TC), and bisphenol A (BPA). The results indicated that the photocatalytic activity of the CoTiO3 perovskite was considerably improved by introducing C3N5 nanosheets and fabricating CoTP/C3N5 nanocomposite. The crystalline structure of CoTiO3/C3N5 (CoTP/C3N5) nanocomposites was confirmed successfully by XRD analysis. The specific surface area of the synthesized CoTP/C3N5 nanocomposite was 8.15 m2/g calculated by N2 adsorption–desorption technology. In the 60th minute of the photocatalytic process, the degradation efficiency of MB, TC, and BPA by CoTP/C3N5 were obtained as 98.70, 60.33, and 92.90 %, respectively, which were higher than pristine CoTiO3 nanorods and C3N5 nanosheets. Electrochemical impedance analysis shows that the CoTP/C3N5 nanocomposite has good electrochemical performance. The improvement photocatalytic activity CoTP/C3N5 can be attributed to the suppressing the recombination of photogenerated electrons and holes and good electrochemical performance with high electron transfer capability. The results achieved from UV–Visible Diffused Reflectance Spectroscopy (DRS), mott-schottky measurements and the photocatalytic degradation experiments in the presence of scavengers confirmed the significantly accelerating the Z-scheme charge transfer mechanism where photoexcited carriers can migrate between CoTiO3 perovskite and C3N5 nanosheets.

Assessment of Microplastics in Hanumante River of Kathmandu Valley

Plastic debris is one of the most significant organic pollutants in the aquatic environment. Researchers are currently focusing on the impact of micro and nano-scale plastic waste on aquatic systems. In this study, we investigated the distribution of plastic pellets and fragments present in the freshwater ecosystem. The goal was to assess microplastic (MP) abundance in the Hanumante River, a tributary of the Bagmati River, and analyze their properties. Sample collection involved the bottle sampling method. Filtration, wet peroxide oxidation, density separation, gravimetric analysis, and microscopic examination were performed to study the characteristics of microplastics. The study was conducted by following the guidelines of the National Oceanic and Atmospheric Administration (NOAA) protocol. Gravimetric analysis was applied to calculate the reduced mass of the sample after total organic carbon reduction. Results showed that the maximum amount of reduced sample was obtained from the sample taken from sample taken from Madhyapur Thimi area (~3.593g) and the minimum amount of reduced sample was obtained from the sample taken from the Shiva temple Jagati area (~2.130g). Microscopic inspection showed that samples taken from different locations were composed of an average of 14–23 microplastics per liter of sample. FT-IR analysis was performed to analyze the characteristics of microplastics and the type of polymers present in the sample which showed the abundance of polymer materials like polyethylene, polypropylene, and polycarbonates. The findings imply that appropriate plastic waste management measures be implemented in the communities to safeguard the ecosystem benefits derived from the river.

Wavelength-dependent direct and indirect photochemical transformations of organic pollutants

Sunlight-induced photochemical transformations greatly affect the persistence of organic pollutants in natural environment. Whereas sunlight intensity is well-known to affect pollutant phototransformation rates, the reliance of pollutant phototransformation kinetics on sunlight spectrum remains poorly understood, which may greatly vary under different spatial-temporal, water matrix, and climatic conditions. Here, we systematically assessed the wavelength-dependent direct and indirect phototransformations of 12 organic pollutants. Their phototransformation rates dramatically decreased with light wavelength increasing from 375 to 632 nm, with direct photolysis displaying higher wavelength-dependence than indirect photolysis. Remarkably, UV light dominated both direct (90.4–99.5 %) and indirect (64.6–98.7 %) photochemical transformations of all investigated organic pollutants, despite its minor portion in sunlight spectrum (e.g., 6.5 % on March 20 at the equator). Based on wavelength-dependent rate constant spectrum, the predicted phototransformation rate of chloramphenicol (4.5 ± 0.7 × 10−4 s−1) agreed well with the observed rate under outdoor sunlight irradiation (4.3 ± 0.0 × 10−4 s−1), and there is no significant difference between the predicted rate and the observed rate (p-value = 0.132). Moreover, rate constant and quantum yield coefficient (QYC) spectrum could be applied for facilely investigate the influence of spectral changes on the phototransformation of pollutants under varying spatial-temporal (e.g., season, latitude) and climatic conditions (e.g., cloud cover). Our study highlights the wavelength-dependence of both direct and indirect phototransformation of pollutants, and the UV part of natural sunlight plays a decisive role in the phototransformation of pollutants.

Green synthesis of CuO/Fe2O3/ZnO ternary composite photocatalyst using grape extract for enhanced photodegradation of environmental organic pollutant

This research delves into fabricating a CuO/Fe2O3/ZnO (CFZ) ternary composite photocatalyst, employing grape extract for its eco-conscious synthesis. The method intricately integrates copper acetate, ferric nitrate, and zinc acetate as precursor compounds, harmonizing them with grape extract serving as a green reducing agent. Meticulous microwave treatment and controlled calcination orchestrate the nuanced formation of the desired composite material. The extensive characterization, involving X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), energy-dispersive X-ray spectroscopy (EDXS), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) surface area analysis, ultraviolet–visible diffuse reflectance spectroscopy (UV-DRS), and photoluminescence (PL) spectroscopy, unveils an array of favorable physical, chemical, and optical attributes conducive to proficient photocatalysis. Notably, CFZ–10mc showcases a narrower bandgap of 1.91 eV, which is pivotal for bolstering electron–hole separation, thereby enhancing its photocatalytic efficacy. Assessment of CFZ's performance in degrading Rhodamine B (RhB) under UV irradiation highlights an impressive 88.8% degradation efficiency within 120 min, accompanied by a kinetic rate constant of 1.81 × 10−2 min−1. Deliberation upon crucial parameters, including photocatalyst dosage, initial RhB pH, and reactor energy consumption, introduces the electrical energy per order (EEO) as a notable efficiency metric. CFZ manifests a substantial reduction in operational costs, estimated to be 18.10 times lower than conventional photolysis, signifying an EEO value of 509.17 kWh m−3 order−1. Optimal operational conditions propose a photocatalyst content of 1.5 g L−1 and an initial RhB pH of 7, fostering the prevalence of the primary active species, •OH. These findings illuminate CFZ's potential in mitigating organic pollutants, underlining its pivotal role in sustainable water remediation. Additionally, practical implementation guidelines for leveraging CFZ's capabilities in real-world applications are presented with care and consideration.

Micro(nano)plastics: invisible compounds with a visible impact

The plastic related research has been an epicentre in recent times. The presence and spread of micro (nano) plastics (MNPs) are well-known in the terrestrial and aquatic environment. However, the focus on the fate and remediation of MNP in soil and groundwater is limited. The fate and bioaccumulation of ingested MNPs remain unknown within the digestive tract of animals. There is also a significant knowledge gap in understanding the ubiquitous organic environmental pollutants with MNPs in biological systems. Reducing plastic consumption, improving waste management practices, and developing environmentally friendly alternatives are some of the key steps needed to address MNP pollution. For better handling and to protect the environment from these invisible substances, policymakers and researchers urgently need to monitor and map MNP contamination in soil and groundwater.

Perfluorooctane sulfonate causes pyroptosis and lipid metabolism disorders through ROS-mediated NLRP3 inflammasome activation in grass carp hepatocyte

The surfactant perfluorooctane sulfonate (PFOS) is widely produced worldwide. It is a persistent organic pollutant in the aquatic environment and poses a serious threat to aquatic organisms, as PFOS exposure can cause liver injury in a wide range of organisms. However, it is unclear whether PFOS exposure-induced hepatocellular injury in fish is associated with ROS-mediated activation of NLRP3 inflammasome. In this study, various PFOS concentrations were applied to L8824 cells, a cell line of grass carp hepatocytes. The detrimental impacts of PFOS on oxidative stress, pyroptosis, lipid metabolism, and the discharge of inflammatory factors were examined. MCC950 and N-acetylcysteine were employed to hinder the PFOS-stimulated activation of the NLRP3 inflammasome and the excessive generation of reactive oxygen species in L8824 cells, respectively. This study demonstrated that treatment with PFOS resulted in oxidative stress and activation of NLRP3 inflammasome in L8824 cells. This led to increased expression levels of indicators related to pyroptosis, accompanied by the upregulation of pro-inflammatory cytokine expression as well as downregulation of anti-inflammatory factors. In addition, following PFOS exposure, the expression levels of genes related to lipid synthesis were upregulated and lipid catabolism-related genes were downregulated. Surprisingly, both N-acetylcysteine and MCC950 interventions significantly reduced PFOS-induced L8824 cell pyroptosis and lipid metabolism disorders. In conclusion, this research demonstrated that PFOS drives NLRP3 inflammasome activation through oxidative stress induced by reactive oxygen species overload. This in turn leads to pyroptosis and lipid metabolism disorders.

Biochar improved the solubility of triclocarban in aqueous environment: Insight into the role of biochar-derived dissolved organic carbon

Biochar as an effective adsorbent can be used for the removal of triclocarban from wastewater. Biochar-derived dissolved organic carbon (BC-DOC) is an important carbonaceous component of biochar, nonetheless, its role in the interaction between biochar and triclocarban remains little known. Hence, in this study, sixteen biochars derived from pine sawdust and corn straw with different physico-chemical properties were produced in nitrogen-flow and air-limited atmospheres at 300–750 °C, and investigated the effect of BC-DOC on the interaction between biochar and triclocarban. Biochar of 600∼750 °C with low polarity, high aromaticity, and high porosity presented an adsorption effect on triclocarban owing to less BC-DOC release as well as the strong π-π, hydrophobic, and pore filling interactions between biochar and triclocarban. In contrast and intriguingly, biochar of 300∼450 °C with low aromaticity and high polarity exhibited a significant solubilization effect rather than adsorption effect on triclocarban in aqueous solution. The maximum solubilization content of triclocarban in biochar-added solution reached approximately 3 times its solubility in biochar-free solution. This is mainly because the solubilization effect of BC-DOC surpassed the adsorption effect of biochar though the BC-DOC only accounted for 0.01–1.5 % of bulk biochar mass. Furthermore, the high solubilization content of triclocarban induced by biochar was dependent on the properties of BC-DOC as well as the increasing BC-DOC content. BC-DOC with higher aromaticity, larger molecular size, higher polarity, and more humic-like matters had a greater promoting effect on the water-solubility of triclocarban. This study highlights that biochar may promote the solubility of some organic pollutants (e.g., triclocarban) in aqueous environment and enhance their potential risk.

Evaluation of the persistent organic pollutants association with type 2 diabetes: A prospective study from Karachi, Pakistan.

The aim of this study is to determine the association between environmental organic pollutants with type 2 diabetes. This prospective study was conducted in Federal Urdu University of Arts, Science and Technology (FUUAST) Gulshan-e-Iqbal Campus Karachi in duration from January 2016 to June 2017. This study was ethically approved from the Institutional Review Board of FUUAST. The study included 50 male and female convenient subjects with type 2 diabetes. Subject with other type of diabetes was excluded. Consent was obtained by each individual. Self-structured questionnaire was used for data collection. The comparative results suggest that the maximum level of summation polychlorinated biphenyls (PCBs) mean value was found in age group 27-33 as 0.695 mg/kg in 73% having total individual eleven. Median (interquartile range) of pesticides levels among subjects with normal weight, over weight and obesity were 0.49 (0.26-2.13), 1.53 (0.60-2.65), and 1.60 (1.23-2.05) respectively. It was observed that Organochlorine pesticides (OCS) levels of subjects with overweight and obesity were almost similar (P-value > 0.05) but significantly higher as compared to subjects with normal weight (P-value < 0.05). No significant differences were observed between PCB levels of subjects in terms of body mass index (BMI). In present study we trace the important elements involve in the deposition of persistent organic pollutants and established an association between pollutants with etiology of diabetes and associated disorders such as obesity.

Characterization of O2 uncoupling in biodegradation reactions of nitroaromatic contaminants catalyzed by rieske oxygenases.

Rieske oxygenases are known as catalysts that enable the cleavage of aromatic and aliphatic C-H bonds in structurally diverse biomolecules and recalcitrant organic environmental pollutants through substrate oxygenations and oxidative heteroatom dealkylations. Yet, the unproductive O2 activation, which is concomitant with the release of reactive oxygen species (ROS), is typically not taken into account when characterizing Rieske oxygenase function. Even if considered an undesired side reaction, this O2 uncoupling allows for studying active site perturbations, enzyme mechanisms, and how enzymes evolve as environmental microorganisms adapt their substrates to alternative carbon and energy sources. Here, we report on complementary methods for quantifying O2 uncoupling based on mass balance or kinetic approaches that relate successful oxygenations to total O2 activation and ROS formation. These approaches are exemplified with data for two nitroarene dioxygenases (nitrobenzene and 2-nitrotoluene dioxygenase) which have been shown to mono- and dioxygenate substituted nitroaromatic compounds to substituted nitrobenzylalcohols and catechols, respectively.

A S-type 2D/2D heterojunction via intercalating ultrathin g-C3N4 into NH4V4O10 nanosheets and the boosted removal of ciprofloxacin

Exploring cheap, eco-friendliness, and highly efficiency photocatalysts for improving the degradation performance of ciprofloxacin (CIP) is a challenge in the environmental remediation field. Herein, 2D/2D ultrathin g-C3N4/NH4V4O10 (CNNS/NH4V4O10) heterojunction is successfully prepared by intercalating g-C3N4 nanosheets into the ultrathin NH4V4O10 nanobelts. For the optimized 50-CNNS/NH4V4O10, the removal rate is 92% for 10 mg·L−1 CIP under simulated solar light, far better than the separated components CNNS and NH4V4O10. Moreover, the wide degraded concentration of CIP ranges from 5 to 40 mg·L−1 devotes a prospect of practical application. The mechanism investigation confirms the intercalating action can break the interlaminar bonding linkage of NH4, which increases the surface NH4+ content and promotes the steered adsorption capacity toward ciprofloxacin through binding to F- in CIP via H-bonding. This work provides a novel design idea for constructing 2D/2D intercalated nanocomposite for the application in the removal of the deleterious fluoric-containing organic pollutants in water environment.

Persistent Organic Pollutants in Environment and Human Health

Persistent organic pollutants (POPs) are often referred to as "silent killers" due to their bio accumulative and long-term persistence. These can be found in every living thing, from plants to animals to people. These are to culprits for several environmental and human health problems. POPs are a leading cause of diabetes, obesity, endocrine disruption, cancer, cardiovascular disease, reproductive problems, and environmental damage. POP pollution and dangers are of concern to scientists, governments, and NGOs alike. This article reviews the most recent findings about the effects of POP contamination on human health and the natural environment.

Degradation of Ciprofloxacin in Water by Magnetic-Graphene-Oxide-Activated Peroxymonosulfate.

Antibiotics are extensively applied in the pharmaceutical industry, while posing a tremendous hazard to the ecosystem and human health. In this study, the degradation performance of ciprofloxacin (CIP), one of the typical contaminants of antibiotics, in an oxidation system of peroxymonosulfate (PMS) activated by magnetic graphene oxide (MGO) was investigated. The effects of the MGO dosage, PMS concentration and pH on the degradation of CIP were evaluated, and under the optimal treatment conditions, the CIP degradation rate was up to 96.5% with a TOC removal rate of 63.4%. A kinetic model of pseudo-secondary adsorption indicated that it involves an adsorption process with progressively intensified chemical reactions. Furthermore, the MGO exhibited excellent recyclability and stability, maintaining strong catalytic activity after three regenerative cycles, with a CIP removal rate of 87.0%. EPR and LC-MS experiments suggested that •OH and SO4-• generated in the MGO/PMS system served as the main reactants contributing to the decomposition of the CIP, whereby the CIP molecule was effectively destroyed to produce other organic intermediates. Results of this study indicate that organic pollutants in the aqueous environment can be effectively removed in the MGO/PMS system, in which MGO has excellent catalytic activity and stabilization for being recycled to avoid secondary pollution, with definite research value and application prospects in the field of water treatment.

The urinary level of 2,4,5-trichlorophenol was positively associated with both all-cause and cause-specific mortalities in general adult residents of United States

Chlorophenols are widespread environmental organic pollutants with harmful effects on human beings. Although relationships between chlorophenols and various dysfunctions/diseases have been reported, the contribution of chlorophenols exposure to mortalities is underdetermined. In this cohort study, we included 4 types of urinary chlorophenols, aiming to estimate associations of chlorophenols exposure with all-cause and cause-specific mortalities. Urinary chlorophenols were examined at baseline of National Health and Nutrition Examination Survey (NHANES) 2003–2010, and adjusted for the urinary creatinine level. Associations between chlorophenols and mortalities were estimated using COX regression analyses, results were shown as hazard ratio (HR) and 95% confidence interval (95% CI). By dividing participants into four subgroups based on quartiles of urinary levels of chlorophenols, associations between mortalities and categorical variables of chlorophenols were estimated. Furthermore, the quantile g-computation analysis was used to estimate the joint effects of 4 chlorophenols on mortalities. Among 5817 adults (2863 men), 1034 were deceased during the follow-up. After adjusted for confounders, 2,4,5-trichlorophenol (2,4,5-TCP) was found to be positively associated with both all-cause (HR = 1.46; 95% CI: 1.16, 1.84) and cardiovascular disease (CVD) mortalities (HR = 1.60; 95% CI: 1.00, 2.55). Compared to the subgroup of the lowest level of chlorophenols, participants in subgroups of higher 2,4,5-TCP levels showed higher risk of all-cause mortality (P-value for trend = 0.003). For CVD mortality, HRs in subgroups of higher levels of 2,4-dichlorophenol (2,4-DCP) and 2,4,6-trichlorophenol (2,4,6-TCP) were statistically significant (P-values for trend were 0.017 for 2,4-DCP and 0.049 for 2,4,6-TCP). The HRs (95% CI) of joint effects of 4 chlorophenols were 1.11 (1.01, 1.21) and 1.32 (1.10, 1.57) for all-cause and CVD-specific mortalities, and 2,4,5-TCP showed the highest weight in joint effects. All of these findings implied that among 4 urinary chlorophenols we included, 2,4,5-TCP might be a sensitive one in associations with mortalities among general populations.

Selective cascade activation of polycyclic aromatic hydrocarbons in human cells: Role of enzyme's intrinsic electric field

Polycyclic aromatic hydrocarbons (PAHs) are major environmental organic pollutants. Some metabolites of PAHs show greater toxicity to humans while the others do not. It is highly important to decipher PAHs' regioselective activation mechanism and identify the major metabolites to accurately evaluate their public health risk. Here, we have performed a thorough computational study of benzo[a]anthracene (BA) metabolized by P450 1A1 by employing molecular docking, molecular dynamics simulations, quantum chemical calculation, and quantum mechanics/molecular mechanics calculations. Our findings show that highly-reactive species such as 3,4-epoxide, 8,9-epoxide, 3,4-diol-1,2-epoxide, and 8,9-diol-10,11-epoxide were major metabolites, which can efficiently react with guanine and damage DNA with extremely low energy barrier, therefore, supports the regioselective metabolism of BA. The origin of this selective activation is mainly contributed to both the oxygen‑carbon distance and previously overlooked enzyme's intrinsic electric field. Consequently, based on the resolved activation selectivity of BA. We built a high-throughput strategy to efficiently predict the metabolites of other PAHs. The accuracy of the strategy is validated by studying 16 PAHs on the priority control list. Hopefully this will aid the accurate evaluation of public health risks associated with PAH emissions.

A comprehensive assessment framework for the risk and source of polycyclic aromatic hydrocarbons (PAHs) using two weight of evidence (WOE) approaches in bays of Shandong Province, China

Polycyclic aromatic hydrocarbons (PAHs) are one of the most widely distributed typical persistent organic pollutants (POPs) in the global environment, and the high PAHs pollution level worldwide calls for the establishment of environmental risk assessment and source analysis techniques for effective control. Here, we selected four bays of Shandong Province, one of the areas in China with the severest emissions of PAHs, as the research area, and chose clam Ruditapes philippinarum as the sentinel species, to systematically assess the ecological risk, bioeffects, and health risks of PAHs, identify their sources, and establish a comprehensive assessment framework for marine POPs using weight of evidence (WOE) approach. Taken together, ecological, bioeffect, and health risk assessments for marine POPs were integrated using Sediqualsoft model of WOE in seawater and sediment, and the overall risk level of PAHs in Shandong coastal area was ‘Moderate’. Meanwhile, the primary source of PAH was analyzed based on socio-economic parameters using a WOE framework, which was mainly derived from traffic and coal in seawater and sediment, respectively. Collectively, a comprehensive framework for assessing risk and source of marine POPs was built for the first time, and it may be applicable to other environments and pollutants.

Differences among active toluene-degrading microbial communities in farmland soils with different levels of heavy metal pollution.

Heavy metals can severely influence the mineralisation of organic pollutants in a compound-polluted environment. However, to date, no study has focused on the effects of heavy metals on the active organic pollutant-degrading microbial communities to understand the bioremediation mechanism. In this study, toluene was used as the model organic pollutant to explore the effects of soils with different levels of heavy metal pollution on organic contaminant degradation in the same area via stable isotope probing (SIP) and 16S rRNA high-throughput sequencing. Heavy metals can seriously affect toluene biodegradation and regulate the abundance and diversity of microbial communities. SIP revealed a drastic difference in the community structure of active toluene degraders between the unpolluted and heavy metal-polluted soils. All SIP-identified degraders were assigned to nine bacterial classes, among which Alphaproteobacteria, Gammaproteobacteria, and Bacilli were shared by both treatments. Among all active degraders, Nitrospira, Nocardioides, Conexibacteraceae, and Singulisphaera were linked to toluene biodegradation for the first time. Notably, the type of active degrader and microbial diversity were strongly related to biodegradation efficiency, indicating their key role in toluene biodegradation. Overall, heavy metals can affect the microbial diversity and alter the functional microbial communities in soil, thereby influencing the removal efficiency of organic contaminants. Our findings provide novel insights into the biodegradation mechanism of organic pollutants in heavy metal-polluted soils and highlight the biodiversity of microbes involved in toluene biodegradation in compound-polluted environments.

Non-invasive biomonitoring of infant exposure to environmental organic pollutants in north-western Spain based on hair analysis. Identification of potential sources

Recent years have seen growing interest in hair sample analysis to detect organic pollutants (OPs). This biological matrix can be analysed non-invasively for biomonitoring of OPs over a wide exposure window. Obtaining hair sample amounts that meet the needs of the analytical methodology required for the determination of the POs of interest can be challenging, especially in infants. As a result, studies assessing organic pollutants in infant hair have been very scarce. We quantified levels of about 60 OPs, including persistent organic pollutants (POPs), in 110 hair samples from a patient cohort (60 mothers and 50 infants) from Santiago de Compostela (north-western Spain). For each participant we examined relationship between OP levels and corresponding epidemiological parameters using correlations, principal component analysis (PCA), hierarchical cluster analysis, and Multivariate analysis of variance (MANOVA). For many OPs we observed significant correlations with place of residence, parity, and maternal age, as well as pet ownership. Evaluation of dietary habits showed significant associations between levels some OPs and the consumption of fish, molluscs, and cereal. There were significant associations between chlorpyrifos and deltamethrin levels and infant birth characteristics such as birthweight and head circumference. Relations between OP levels in the hair of mothers and their infants were also examined, revealing common sources of exposure for dioxin-like polychlorinated biphenyls (DLPCBs), non-dioxin-like polychlorinated biphenyls (NDLPCBs), polybrominated diphenyl ethers (PBDEs), and polycyclic aromatic hydrocarbons (PAHs). Levels of fluoranthene (F), pyrene (P), endrin, and some PBDEs in maternal hair were significantly correlated with those in infant hair. Our findings identified common sources of exposure to OPs of distinct chemical classes.