Toxic Persistent Organic Pollutants Research Articles

A novel, low-cost, and efficient separation strategy based on S-doped C3N4 for the analysis of PCDD/Fs and dioxin-like PCBs

Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (dl-PCBs) are widespread and highly toxic persistent organic pollutants with similar chemical structure. The popular process for the separation of PCDD/Fs and dl-PCBs in one sample often relies on imported and expensive activated carbon, giving rise to an urgent need of inexpensive and efficient separation method. Herein, a novel, simple, and low-cost separation strategy based on sulfur-doped carbon nitride (S-C3N4) is reported. The S-C3N4 material was synthesized through simple thermal annealing with precursor of thiocyanuric acid. After recovery experiments, the optimal addition ratio of S-C3N4 was determined to be 40% mixed with silica gel. The recoveries for PCDD/Fs and dl-PCBs congeners are 32% - 105% and 60% - 70% respectively, which not only meets USEPA and Chinese standards but also shows comparable performance to activated carbon. Moreover, the proposed S-C3N4 strategy exhibits excellent performance for the analysis of PCDD/Fs and dl-PCBs in real complex samples (sediment and fish liver) in terms of detected concentrations and toxic equivalents. Overall, this study puts forward a new and low-cost avenue for the separation of PCDD/Fs and dl-PCBs, which is of remarkable meaning for motivating the development of detection techniques and domestic equipment for dioxins and other pollutants in the environment.

Controlled construction of 2D hierarchical core-shell ZnO/MnO2 nanosheets on Nitinol fiber with enhanced adsorption performance for selective solid-phase microextraction of trace polycyclic aromatic hydrocarbons in water samples

BackgroundPolycyclic aromatic hydrocarbons (PAHs) are an important class of potentially toxic persistent organic pollutants in environmental water. Their concentrations are usually too low to allow for direct determination with analytical instruments, and the preconcentration is required prior to instrumental analysis. Solid phase microextraction (SPME) is considered as a high-performance green sample preparation technique for volatile and non-volatile organic compounds due to its high enrichment factor. In fact, the nature of SPME coatings governs the adsorption performance. Therefore, more efforts have devoted to the controlled construction of novel long-life SPME fibers with enhanced adsorption performance and improved adsorption selectivity. Results2D hierarchical core-shell ZnO/MnO2 nanosheets (NSs) were constructed on a Nitinol (NiTi) fiber substrate by layer-by-layer assembly for enhanced and selective SPME of PAHs. Firstly, hexagonal ZnO NSs were electrodeposited on the NiTi substrate. Subsequently smaller secondary MnO2 NSs were uniformly grown on the surface of ZnO NSs by a facile hydrothermal oxidation process. ZnO NSs were well protected by the chemically stable MnO2 shell, making the coating highly durable and efficient for SPME application. Meanwhile, the ZnO/MnO2 NSs coating demonstrated superior adsorption performance for PAHs. After the optimization of SPME conditions, the proposed SPME-HPLC-UV method exhibited good analytical performance for preconcentrating and determining trace PAHs with wide linear ranges (0.03–200 μg L−1) and low LODs (0.005–0.112 μg L−1) as well as good repeatability (1.4%-6.9%) and fiber-to-fiber reproducibility (5.3%-7.1%). Moreover, the proposed method showed good precision and recovery in the preconcentration and determination of target PAHs in real water samples. SignificanceAs compared with representative commercially available fibers, the NiTi@ZnO/MnO2 NSs fiber showed enhanced adsorption efficiency and improved adsorption selectivity for PAHs. The constructed fiber can be used as an alternative to commercial fibers for the adsorption and preconcentration of target PAHs in the environmental water samples. Moreover, the preparation strategy is expected to provide new insights into the precisely controlled construction of the efficient and stable core-shell bimetallic oxide nanostructures on the superielastic NiTi-based fibers.

Alteration of biomass toxicity in torrefaction – A XDS-CALUX bioassay study

Torrefaction constitutes one of the promising technologies for the management of waste biomass and the production of high-carbon products for combustion, gasification, adsorption of pollutants or soil treatment. Unfortunately, waste biomass may be contaminated with toxic persistent organic pollutants, such as polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/PCDF) and dioxin-like biphenyls (dl-PCB). Literature does not provide consistent measurements on how the low-temperature thermochemical processing, such as torrefaction, affects the toxicity of biomass. This contribution assesses how a torrefaction treatment, conducted at 200 °C, modifies the toxicity due to PCDD/PCDF/dl-PCB in biomass. We deploy the XDS-CALUX biotest on five types of waste biomass (sewage sludge, tree bark, cattle manure, spent coffee ground, common reed), before and after treatment. The content of total dioxin- & biphenyl fraction compounds in the raw biomass, investigated in this study, varies from 0.14 to 3.67 pg BEQ·g−1d.m., and in the torrefied biomass between 0.17 and 6.00 pg BEQ·g−1d.m.; BEQ stands for bioanalytical equivalent. This increase is statistically insignificant at p = 0.05, taking into account all types of examined biomass. This proves that low-temperature torrefaction cannot detoxify biomass, i.e., chars, produced from biomass characterized by elevated concentration of PCDD/PCDF/dl-PCB, will reflect the contamination of the feedstocks. With respect to heavy metals, we conclude that only the content of Cd in biomass, and, to a lesser extent, the abundance of Cu and Fe, modify the toxicity of this material during its thermochemical treatment at low temperature.

Recent advances in the elimination of persistent organic pollutants by photocatalysis

The non-ending needs of growing human population are being met by rapid industrialization and globalization, which have nowadays become an indispensable component of growth. Although these activities have led to phenomenal growth of the human civilization, at the same time, they have resulted in severe environmental pollution by discharge of highly toxic waste. This waste is severely detrimental not only for the environment but also for the health of the human population. Among different classes of pollutants, one being considered as one of the highly toxic ones is that of persistent organic pollutants (POPs). Advanced oxidation technologies (AOTs) play a major role in the degradation of pollutants by converting organic pollutants into CO2, H2O, and mineralized inorganic ions. AOTs include UV-based photocatalysis, ozonation, electrochemical oxidation, and Fenton and Fenton-like processes There are some difficulties and challenges associated with AOT, such as being highly capital intensive and high consumption of energy. To overcome these bottlenecks, photocatalytic degradation is a promising method that uses solar energy for the degradation of such pollutants. Photocatalysis is further classified into homogenous and heterogenous photocatalysis. As a part of heterogenous photocatalysis, semiconductor photocatalysts have received great attention; but because of their drawbacks such as the recombination of the electron/hole pair, low adsorption rate, and low surface area coverage, nanotechnology was considered for bringing a novel and enhanced remediation photocatalysis process. To this end, the designing of a more efficient photocatalyst by modifying morphology, composition, and structure and reducing toxicity is the need of the hour for the abatement of environmental pollutants. This review focuses on the degradation and removal of highly toxic persistent organic pollutants by using photocatalytic degradation with a detailed account of the various pollutants, their degradation mechanism, process shortcomings, remedial measures, and future prospects.

Legacy and emerging poly- and perfluoroalkyl substances in wastewater treatment plant and receiving water: abundance, removal, and potential ecological risk.

Poly- and perfluoroalkyl substances (PFASs) are toxic persistent organic pollutants and bioaccumulative chemicals, which affect the environment and ecology. PFASs in the wastewater treatment plant (WWTP) and receiving river downstream were investigated. Fourteen out of eighteen PFASs were detected, ranging from 197 to 0.14ng L-1. The main pollutants were 2,3,3,3-tetrafluoro-2-(1,1,2,2,3,3,3-heptafluoro-propoxy) propanoic acid (HFPO-DA), perfluorooctane sulfonate (PFOS), and perfluorooctanoic acid (PFOA). The concentration of HFPO-DA (181ng L-1) was the highest in influent, which indicated the use and emission of PFASs in the sewage collection region of WWTP changed from legacy to emerging ones. However, PFOS from catering wastewater as the main source was dominant PFASs in the reclaimed water. Biological treatment could be effective in the removal of PFASs, especially for HFPO-DA. HFPO-DA could directly bind to cytochrome P450 and bring potential ecotoxicity to the surrounding environment, and the ecological risk of degradation products should be under consideration. Coagulation might result in PFASs release from sludge. More attention should be paid to sewage treatment process decision of WWTP for the control of PFASs.

An exploratory spatial contaminant assessment for polar bear (Ursus maritimus) liver, fat, and muscle from northern Canada

Since the industrial era, chemicals have been ubiquitous in worldwide ecosystems. Despite the discontinued release of highly toxic persistent organic pollutants (POPs) in the environment, the levels of some POPs are still being measured in the Canadian Arctic. These contaminants are of great concern due to their persistence, toxicity, and levels of bioaccumulation in food chains. Animals occupying top trophic positions in the Canadian Arctic, particularly polar bears, are exposed to these contaminants mainly through their diet. Our study investigated the levels of 30 metals (including total and methyl mercury) alkaline and alkaline earth metals, 15 polycyclic aromatic compounds and their alkyl congeners (PACs), 6 chlordanes (CHLs), and 20 polychlorinated biphenyls (PCBs), in 49 polar bears from the Canadian Arctic. Contaminant burden was measured in liver, muscle, and fat in bears of different sex, age, and locations. A principal component analysis did not distinguish differences between age and sex profiles for most contaminants. However, the concentrations measured and their distribution in the tissues confirm findings observed in past studies. This study highlights the importance of continual monitoring of polar bear health (e.g., newly detected PACs were measured within this study) and evaluating those impacts for the next generations of polar bears.

A REVIEW ON MICROPLASTIC IN THE SOILS AND THEIR IMPACT ON SOIL MICROBES, CROPS AND HUMANS

For modern human life, since the beginning of the 21st century, plastic become indispensable. The golden period for the plastic industry was the second half of the 20th century when plastic-based products bucket to the car were manufactured. Due to mismanagement, and indiscriminate use microplastics are emerging as persistent terrestrial pollutants. In the last decade, environmental scientists and other stakeholders have paid serious attention to soil pollution by microplastics. In soils, the microplastic particles act as a vector for the toxic persistent organic pollutants and potentially toxic metals which are easily sorbed by plants and enter the food chain.Microplastic pollutants not only influence the soil’s physicochemical properties but also impact the feeding habits of soil biota. Microplastic in soils is due to sewage sludge, bio waste compost amendments, plastic mulching, wastewater irrigation, leachate from landfills and atmospheric deposition. The quantity of microplastic particles in the soils varied from nil to13000 items per kg of soil. The quantity of microplastic in the soil is 5-23 times that in the ocean. The microplastic in soil retards seed germination and plant growth. Enzymatic activities of the soil are also influenced by microplastic. Plastic Pellets, Personal Care Products and Cosmetics, Synthetic Textiles, the Abrasion of Tyres, City Dust, and the Abrasion of Road Markings etc. are the environmental sources of microplastic. Intake by humans via food causes respiratory toxicity, cytotoxicity, immunotoxicity and reproductive toxicity among other effects. The present work reports the sources and distribution of microplastic in the soil environment and their impact on soil biota, plants, and human health.

Air Mapping of Polycyclic Aromatic Hydrocarbons and Their Uptake by Crops in the Urban Area of Nice, France.

Urban gardening is becoming increasingly popular. Air pollution, which is a major concern in cities might, however, threaten food safety and thus must be assessed. Health risks arise particularly from toxic persistent organic pollutants such as Polycyclic Aromatic Hydrocarbons (PAHs) which are formed by incomplete combustion. A first assessment of crop contamination in two different atmospheric environments in the urban area of Nice reveals a predominance of light PAHs. These pollutants present in the gaseous phase, seem to bioaccumulate while heavy PAHs are absent in vegetation. By understanding the PAH sources and their behavior in the atmosphere but also by analyzing the spatial and temporal data since the European directive in 2004, a link between concentrations found in vegetables grown in experimental gardens and PAH cadastral emission data is presented. The first results could be used as a possible guidance for urban agriculture.

Evaluation and Potential Uses of Site Investigation Soil Contamination Data Submitted to Uk Local Government

There has been considerable brownfield development in the UK since 2000 due to increasing demand for new housing, combined with local opposition to building on greenbelt land. To facilitate this, extensive site investigations have been carried out and the reports submitted to local government as part of the planning process. This research investigates whether this largely untapped resource of site investigation data can be used to improve understanding of potentially toxic elements (PTE) and persistent organic pollutants (POP) at a local scale. The PTE/POP data were extracted from 1707 soil samples across 120 brownfield sites in an urban/suburban region. The samples were analysed to determine the effect of site location, historical use and site age on PTE/POP concentrations. Box plots indicating statistical results together with GIS maps of PTE/POP sample data provided the optimal visualisation of results. The dataset was shown to be a valuable resource, although further exploitation would be enhanced by digitisation of the submitted data. The paper explores potential applications of this data, including background concentrations and anthropogenic enrichment factors for PTE/POP. The results were summarised in a table for the PTE/POP and a preliminary risk assessment process chart to inform developers/regulators on potential PTE/POP levels on brownfield sites on a local scale. This information could focus design and resources for developers for site investigations and risk assessments and improve planning and regulatory guidance. The lack of predictability in PTE/POP results across sites have emphasised the ongoing need for intrusive site investigation on new brownfield developments.

Aggressiveness and Metastatic Potential of Breast Cancer Cells Co-Cultured with Preadipocytes and Exposed to an Environmental Pollutant Dioxin: An in Vitro and in Vivo Zebrafish Study.

Background:Breast cancer (BC) is a major public health concern, and its prognosis is very poor once metastasis occurs. The tumor microenvironment and chemical pollution have been suggested recently to contribute, independently, to the development of metastatic cells. The BC microenvironment consists, in part, of adipocytes and preadipocytes in which persistent organic pollutants (POPs) can be stored.Objectives:We aimed to test the hypothesis that these two factors (2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), an extensively studied, toxic POP and the microenvironment) may interact to increase tumor aggressiveness.Methods:We used a co-culture model using BC MCF-7 cells or MDA-MB-231 cells together with hMADS preadipocytes to investigate the contribution of the microenvironment and 2,3,7,8-tetrachlorodibenzo-p-dioxin TCDD on BC cells. Global differences were characterized using a high-throughput proteomic assay. Subsequently we measured the BC stem cell–like activity, analyzed the cell morphology, and used a zebrafish larvae model to study the metastatic potential of the BC cells.Results:We found that coexposure to TCDD and preadipocytes modified BC cell properties; moreover, it induced the expression of ALDH1A3, a cancer stem cell marker, and the appearance of giant cancer cells with cell-in-cell structures (CICs), which are associated with malignant metastatic progression, that we demonstrated in vivo.Discussion:The results of our study using BC cell lines co-cultured with preadipocytes and a POP and an in vivo zebrafish model of metastasis suggest that the interactions between BC cells and their microenvironment could affect their invasive or metastatic potential. https://doi.org/10.1289/EHP7102

Reverse transcription-loop mediated isothermal amplification (RT-LAMP) assay for detection of AhR receptor responsive xenobiotics

Dioxins are a group of highly toxic environmental persistent organic pollutants, which are lipophilic in nature. 2, 3, 7, 8- tetrachlorodibenzo-p-dioxin (TCDD) is the most toxic representative of this class. TCDD causes several human health effects like endocrine disruption, carcinogenesis and reproductive toxicity mediated by aryl-hydrocarbon receptor. Current detection methods of dioxins like gas chromatography–mass spectrometry, liquid chromatography–mass spectrometry etc. are costly and time consuming. Therefore, the present study aims to develop a relatively faster and cheaper technique called reverse transcription-loop mediated isothermal amplification (RT-LAMP) assay to detect dioxins. Cultured granulosa cells used as a model system were treated with different doses (5, 10 and 15 pg/mL) of aryl hydrocarbon receptor (AhR)responsive xenobiotic, TCDD, in accordance with maximum residue limit values. Cells were treated for 6, 12 and 24 h, respectively to study the gene expression of TCDD receptor called AhR and AhR responsive genes, CYP1A1 and CYP1B1, in a dose and time dependent manner. All targeted genes expression significantly increased after 6 and 12 h by 1.3–8 folds. For the development of RT-LAMP assay, CYP1A1 gene was used with 6 h TCDD treatment. RT-LAMP assay was standardized with optimal color change at 30 min using 50 ng of cellular RNA. In all the cases, we could distinguish RT-LAMP-positive condition from one sample to another sample due to intensity of color. The method was also validated by spectrometric method. In conclusion, the developed method will be used to screen AhR receptor responsive xenobiotics by observing the color change in RT-LAMP assay like dioxin used in the present study.

Environmental perspectives of microplastic pollution in the aquatic environment: a review

Microplastics are a highly concerning pollutant that have gained attention from the scientific community and other regulatory authorities due to their potential risks to organisms and ecosystems. Microplastics are widespread in both terrestrial and aquatic ecosystems and can be found even in Antarctica and deep-sea sediments. The ability to survive for long periods in the environment and their aptitude of inter- and intra-environmental translocation can prompt poor environmental outcomes. The adsorption of heavy metals and other toxic persistent organic pollutants is a further cause for concern. Furthermore, microplastics enable the development of a distinct microbial niche within an ecosystem, which could potentially impair ecosystem function by promoting the growth of selective microbial communities. The acquisition of metal-resistant, antibiotic-resistant genes, and the enrichment of antibiotic-resistant bacteria on microplastic surfaces have recently been reported. Moreover, some studies have also reported the colonization of pathogenic bacterial strains such as Vibrio spp. on microplastic surfaces. This review aims to address the sources of microplastic pollution in the freshwater and marine environments and to discuss their potential functions in the environment.

Inventory of Polychlorinated Naphthalene Emissions from Waste Incineration and Metallurgical Sources in China.

Polychlorinated naphthalenes (PCNs) are highly toxic persistent organic pollutants (POPs) that are a relatively new addition to the Stockholm Convention as of 2015. The levels of unintentional emissions of PCNs from important industrial thermal sources on national scales are unclear but are important for understanding potential human exposure. In this study, an inventory was compiled of PCN emissions from priority industrial sources of unintentional POPs in China. Estimated emissions from four typical POP sources in the reference year (2014) in China were 511.6 kg by mass and 7650.8 mg of toxic equivalent. Waste incineration, secondary nonferrous smelting, electric arc furnace steelmaking, and iron ore sintering plants contributed 38.8, 15.4, 29.2, and 16.6%, respectively, to the total emissions. The Eastern Seaboard of China and the Hebei region in North China, which have intensive industrial activity and high population densities, were dominant contributors of PCNs. Only 18.6% of the counties where waste incineration plants were located emitted PCNs at a level higher than 1.00 × 10-1 mg of toxic equivalent, whereas 80% of the counties where metallurgical plants were located emitted PCNs at this level. These results indicate effective implementation of POP control in the waste incineration industry in China. This study clarifies the unintentionally emission levels of PCNs in China and provides important information for strategy development to control source emissions.

Persistent, bioaccumulative, and toxic properties of liquid crystal monomers and their detection in indoor residential dust

Liquid crystal monomers (LCMs) are used widely in liquid crystal displays (LCDs), which are dramatically changing the world due to the provision of convenient communication. However, there are essentially no published reports on the fate and/or effects of LCMs in the environment. Of 362 currently produced LCMs, 87 were identified as persistent and bioaccumulative (P&B) chemicals, which indicated that these chemicals would exhibit resistance to degradation and exhibit mobility after entering the environment. Following exposure to mixtures of LCM collected from 6 LCD devices, significant modulation of 5 genes, CYP1A4, PDK4, FGF19, LBFABP, and THRSP, was observed in vitro. Modulation of expressions of mRNAs coding for these genes has frequently been reported for toxic (T) persistent organic pollutants (POPs). In LCM mixtures, 33 individual LCMs were identified by use of mass spectrometry and screened for in 53 samples of dust from indoor environments. LCMs were detectable in 47% of analyzed samples, and 17 of the 33 LCMs were detectable in at least 1 sample of dust. Based on chemical properties, including P&B&T of LCMs and their ubiquitous detection in dust samples, the initial screening information suggests a need for studies to determine status and trends in concentrations of LCMs in various environmental matrices as well as tissues of humans and wildlife. There is also a need for more comprehensive in vivo studies to determine toxic effects and potencies of LCMs during chronic, sublethal exposures.

Environmental Applications of Boron‐Doped Diamond Electrodes: 1. Applications in Water and Wastewater Treatment

AbstractOver the past few decades, environmental applications of the boron‐doped diamond (BDD) electrode are reported to be vast and versatile. Applications of BDD electrodes in the field of electrochemical advanced oxidation processes (EAOPs) for the abatement of toxic persistent organic pollutants are significant, owing to the easy and effective way of treatment. This article focuses on highlighting and summarizing the applications of the BDD electrode for the treatment of different synthetic and real wastewaters, such as those involved in pharmaceuticals and personal care products, pesticides/herbicides, dyes, etc. We also review the processes and methodologies involving the synthesis of BDD electrodes and summarize the desirable characteristic features required for the application of EAOPs. Applications of BDD electrodes for the treatment of wastewater through different EAOPs, including anodic oxidation, electro‐Fenton, coupling processes such as electro‐Fenton pyrite, bioelectro‐Fenton, and their recent advancements are also discussed in detail. It envisages the greater potential for complete treatment of different toxic wastewater effluents. This Review shows that the application of BDD electrodes in the field of wastewater treatment is tremendous and proves to be a promising material for future perspectives.

Mechanistic understanding and future prospect of microbe-enhanced phytoremediation of polycyclic aromatic hydrocarbons in soil

Abstract Restoring polluted land is a time-consuming endeavor due to the difficulty inherent in the process. The quality of soil considerably worsens with the addition of toxic persistent organic pollutants (POPs) of industrial origin. Industrialization results in millions of tonnes of POPs worldwide, which pose a threat to surrounding ecosystems. In India alone, oil refineries generate approximately 28,000 tonnes of oily sludge (toxic organic compounds) per annum containing POPs—polycyclic aromatic hydrocarbons (PAHs). These PAHs have existed in environments throughout the globe for the last several decades due to long half-lives. The fate of PAHs and their residues pose a threat to all forms of life. High levels of the 16 PAHs (US EPA) were found in soil in Asia’s oldest oil and gas drilling site, with a range spanning from a minimum of 13.48 to a maximum of 86.3 mgkg − 1 due to exploration of crude oil. The management of such a paradoxical situation is a challenge. The mitigation of PAHs by employing plant–microbe systems from soil is a low-cost prospective biotechnological approach. This technology engineers the rhizosphere and helps restoration of degraded land. Recent findings demonstrated how adding biochar (carbon rich phytoproduct) to the soil resulted in positive effects on plant–microbe assisted PAH removal. This review focuses on the mechanistic understanding of plant–microbe assisted remediation. We consider the future prospect to optimize the phytoremediation process through genomics and metabolomics data. The genetic manipulation of plants and microbes seems to have improved the phytoremediation process by utilizing the signaling network of plant–microbe interactions

Signatures of chlorinated dioxins and furans along the exposure path – The relation between vegetation and soil

Polychlorinated dibenzo-p-dioxins and dibenzo-furans (PCDD/Fs) belong to the most toxic persistent organic environmental pollutants. Therefore, knowledge about their fate along the exposure path is of special concern. In order to comprehend the transfer of PCDD/Fs across different environmental compartments, PCDD/F concentrations in plants and in soil were evaluated. Pairs of soil and plant samples were selected according to the shortest distance between sampling points. At 15 sites PCDD/F concentrations in spruce needles and in forest humus layers where compared. Summer conditions were evaluated on the basis of 8 sites with ryegrass- and grassland topsoil samples. Autumn conditions were addressed using 7 sites with curly kale and topsoil samples under grassland. Correlation analyses of the PCDD/F congener profiles for plant- and soil samples were conducted. The correlations were compared to influencing site (e.g. local temperature) and spatial as well as temporal offset parameters. No governing parameter that decisively influenced the similarity between plant and soil signature became evident. By means of the toxicity factors of TEQ-WHO, tetra- and penta-PCDD/F homologues were assigned to the group of low-chlorinated homologues (lcH), and hexa-, hepta- and octa-PCDD/F homologues to the high-chlorinated homologues (hcH). lcH and hcH are presumed to differ in solubility, volatility and rate of degradation. The ratio of lcH/hcH revealed characteristic fingerprints that enabled the differentiation of the individual PCDD/F-plant and -soil pairs. Spruce-humus pairs showed a close relation during winter exposure times, while the lower summer concentrations were not reflected in the humus layer. Kale was exposed at the beginning of the season with elevated PCDD/F immissions, and showed a closer relation to grassland topsoil than did ryegrass. lcH/hcH proved as a simple criterion that can reveal related PCDD/F fingerprints of different environmental compartments despite signal attenuation due to decomposition, volatilization and particulate transport.

Biochar-mediated regulation of greenhouse gas emission and toxicity reduction in bioremediation of organophosphorus pesticide-contaminated soils

Abstract Organophosphorus pesticides (OPPs) are a set of toxic persistent organic pollutants (POPs) present in the environment. Recently, biochar-mediated bioremediation has exhibited many advantages over conventional methods for the remediation of pesticide-contaminated soil. In the present study, biochar and nitrogen fertilizer (NH4NO3) were employed to remediate OPP-contaminated soil and the greenhouse gas (GHG) emission during 90 days of incubation was investigated. After thermal desorption treatment, the content of organophosphorus pesticides reduced from 175.61 μg·kg− 1 to 62.68 μg·kg− 1. The addition of NH4NO3 in the following bioremediation led to larger reduction (34.35%) of the pesticide concentration than that of biochar (31.90%) for the contaminated soils with thermal desorption treatment, while the simultaneous addition of biochar and NH4NO3 led to the largest reduction of pesticide concentration (11.07%) for the soil without thermal desorption treatment. The addition of biochar and NH4NO3 only slightly increased the emission rate of GHGs from the soil without thermal treatment, but remarkably increased the emission rate of GHGs from the soil after thermal treatment. In most cases, the addition of NH4NO3 is more effective than biochar to promote the degradation of pesticide, but also exhibited higher GHG emission. The microbial community analysis suggests that the enhanced degradation of pesticide is mainly owing to the increased activity of microorganism.

Arabidopsis plants exposed to dioxin result in a WRINKLED seed phenotype due to 20S proteasomal degradation of WRI1.

Dioxins are highly toxic persistent organic pollutants bioaccumulated by both plants and animals that cause severe developmental abnormalities in humans. We investigated the effects of dioxins on seed development in Arabidopsis. Plants were exposed to various concentrations of the most toxic congener of dioxins, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and the effects on seed development were analysed in-depth at transcriptome, proteome and metabolome levels. Exposure to dioxin led to generalized effects on vegetative tissues plus a specific set of perturbations to seed development. Mature seeds from TCDD-treated plants had a characteristic 'wrinkled' phenotype, due to a two-thirds reduction in storage oil content. Transcriptional analysis of a panel of genes related to lipid and carbohydrate metabolism was consistent with the observed biochemical phenotypes. There were increases in WRI1 and LEC1 expression but decreases in ABI3 and FUS3 expression, which is puzzling in view of the low seed oil phenotype. This anomaly was explained by increased expression of 20S proteasome components that resulted in a substantial degradation of WRI1 protein, despite the up-regulation of the WRI1 gene. Our findings reveal novel effects of dioxins that lead to altered gene regulation patterns that profoundly affect seed development in Arabidopsis.

Estimating national dioxins and furans emissions, major sources, intake doses, and temporal trends in Iran from 1990\u20132010

BackgroundPolychlorinated dibenzo-p-dioxins (PCDD) and dibenzofurans (PCDFs) are highly toxic persistent organic pollutants (POPs), which can cause various health outcomes, such as cancer. As a part of the National and Sub-national Burden of Disease Study (NASBOD), we aimed to estimate dioxins and furans national emissions, identify their main sources, estimate daily intake doses, and assess their trend from 1990–2010 in Iran.MethodsThe Toolkit for Identification and Quantification of Releases of Dioxins, Furans and Other Unintentional POPs, which is developed by the United Nations Environment Programme (UNEP 2013), was used to estimate the emissions of PCDD/PCDFs from several sources into the air, water, land, residue, and other products. The daily intake doses were estimated using a linear regression of estimated emissions by UNEP Toolkit and average intake doses in other countries. Finally, the trend of PCDD/PCDFs emissions and daily intake doses were explored from 1990–2010.ResultsThe total emissions were estimated as 960 g Toxic Equivalents (g TEQ) for 1990 and 1957 g TEQ for 2010 (18.2 and 26.8 g TEQ per million capita, respectively). The estimations suggest that albeit contribution of open burning to PCDD/PCDFs emissions has been declining from 1990 to 2010, it remained the major source of emissions in Iran contributing to about 45.8% out of total emissions in 1990 to 35.7% in 2010. We further found that PCDD/PCDFs are mostly emitted into the ambient air, followed by residue, land, products, and water. The daily intake doses were estimated to be 3.1 and 5.4 pg TEQ/kg bw/day for 1990 and 2010, respectively. We estimated an increasing trend for PCDD/PCDFs emissions and intake doses in Iran from 1990–2010.ConclusionsThe high levels of emissions, intake doses, and their increasing trend in Iran may pose a substantial health risk to the Iranian population. Further studies with more rigorous methods are recommended but this should not circumvent taking appropriate policy actions against these pollutants. Currently, Iran has no standard for dioxins and furans. Adaptation of the World Health Organization recommended guidelines might be an appropriate starting point to control dioxins and furans emissions.