PAH contamination in road dust from a moderate city in North China: The significant role of traffic emission

To investigate the contamination level, distribution, possible source, and human exposure risk of polycyclic aromatic hydrocarbons (PAHs) in the urban traffic environment, 15 PAHs were measured in 34 road dust samples (particle size < 25 μm) collected from three grades of roads and park paths in Xinxiang, China. ΣPAHs concentrations ranged from 311 to 21200 ng g^?1, with a mean of 5890 ng g^?1 and decreased in the following order: main roads (7650 ng g^?1) > collector streets (7410 ng g^?1) > bypasses (2970 ng g^?1) > park paths (1570 ng g^?1), indicating that significant positive correlation existed between PAH contamination and traffic density. PAHs in all samples were dominantly composed of 4-ring PAHs, accounting for 44.8% of the total. Pyrene, fluoranthene, and chrysene were the predominant individual components and accounted for 14.7% (1.2–19.2%), 12.9% (3.3–20.3%), and 11.0% (2.5–18.6%) of ΣPAHs, respectively. The specific isomer ratios indicated that traffic emission was the dominant source of PAHs in road dust. The incremental lifetime cancer risk values showed that cancer risk from exposure to road dust–borne PAHs was acceptable for local residents in Xinxiang.     

DDT and HCH (Organochlorine Pesticides) in Residential Soils and Health Assessment for Human Populations in Korba,India

Dichlorodiphenyltrichloroethane (DDT), hexachlorocyclohexane (HCH), and their isomers’ levels in residential soils were determined for the assessment of health risk in Korba, India. Observed concentrations of total HCH and total DDT in soils were more or less comparable with other parts of India and the world. ΣHCH and ΣDDT concentrations ranged between 0.9–20 μg kg^?1 and 2–315 μg kg^?1, respectively, which were lower than recommended soil quality guidelines indicating low ecotoxicological risk. Carcinogenic and non-carcinogenic impacts of HCH and DDT on human populations through soil ingestion were evaluated and presented. The incremental lifetime cancer risk (ILCR) for adults and children ranged between 7.8 × 10^?10–1.6 × 10^?7 and 4.1 × 10^?9–8.2 × 10^?7, respectively. Non-cancer health hazard quotient (HQ) ranged between 5.9 × 10^?7–1.8 × 10^?3 and 3.1 × 10^?6–9.4 × 10^?3, respectively, for adults and children. The estimated ILCR and HQ were within the safe acceptable limits of 10^?6–10^?4 and ≤1.0, respectively, indicating low risk to human populations from exposure to organochlorine pesticides (HCH and DDT) in the study area.     

Polycyclic Aromatic Hydrocarbon (PAH) Contamination in the Urban Topsoils of Shenyang,China

Polycyclic aromatic hydrocarbons (PAHs) in the surface urban soils of Shenyang in Northeastern China were investigated. The total concentration of the PAHs ranged from 0.09 to 8.35 mg kg^?1, with an average value of 1.51 ± 1.64 mg kg^?1. 3–5-ring PAHs accounted for 90% of total PAHs. The functional areas, such as the industrial regions (4.95 mg kg^?1) and main roads (1.56 mg kg^?1), as well as the administrative divisions, including the districts of Shenhe (1.49 mg kg^?1), Heping (2.08 mg kg^?1), and Tiexi (2.14 mg kg^?1), were heavily polluted by PAHs. The diagnostic ratios and principal component analysis (PCA) for PAHs indicate that the pollutants probably originated primarily from coal combustion and petroleum sources. The Nemerow composite index, used to assess environmental quality, shows that the soil samples were heavily polluted with PAHs, and although 52.8% of the soil sampling sites were safe, 47.2% of the soil sampling sites registered different grades of PAH pollution. The PAH contamination in Shenyang emphasizes the need for controlling fossil fuel combustion and traffic exhaust.     

Occurrence and risk assessment of organophosphorus pesticide residues in Chinese tea

Tea is the second widely consumed beverage next to water. Tea drinking is one of the important pathways for human exposure of organonphosphorus pesticide. Consequently, incidence of organonphosphorus pesticide residues and risk assessment should be clear. In this study, the level of organonphosphorus pesticide residues in 810 Chinese teas manufactured between 2010–2013 was investigated using gas chromatography coupled with tandem mass spectrometry and a flame photometric detector. Incidence of organonphosphorus pesticide residues occurred with a frequency of 29% and the average concentration of 93 μg kg^?1. The residue levels varied from tea types, sale spots, and production area. Chlorpyrifos, isocarbophos, and triazophos were the only three organonphosphorus pesticides with detectable residues, and the detectable rates were 13.0%, 13.6%, and 17.4%, respectively. The corresponding average daily intake of chlorpyrifos, isocarbophos, and triazophos by tea drinking was 0.000083 μg kg^?1 bw day^?1, 0.0036 μg kg^?1 bw day^?1, and 0.0022 μg kg^?1 bw day^?1. These results showed that the total hazard quotient of organonphosphorus pesticide pesticides from tea drinking was less than 0.02 and that the tea-drinking originated organonphosphorus pesticide exposure had a little adverse health effect for human being.     

Determination of Glyphosate and AMPA in Three Representative Agricultural Austrian Soils with a HPLC-MS/MS Method

We developed a novel method to quantify adsorbed glyphosate and AMPA in soils based on an extraction utilizing Na-tetraborate, an SPE clean-up step, and subsequent LC-MS detection. Reversed phase-based separation of glyphosate and AMPA was realized after FMOC-derivatization. The quantification involved external calibration and 1,2–¹³C, ¹⁵N- labeled glyphosate as well as ¹³C, ¹⁵N labeled AMPA as internal standards. The optimum recovery for extraction was obtained with 40 mM Na-tetraborate. The method was applied in three representative soils (Kirchberg, Phyra, and Pixendorf, Austria) where glyphosate was applied by standard agricultural practices. The recovery for glyphosate extracted with 40 mM Na-tetraborate buffer was 93.5% (RSD <2%) for glyphosate at Kirchberg-cambisol; 95.7% (RSD < 2%) at Pixendorf- chernozem and 79.1% (RSD <7%) at Phyra-stagnosol. The corresponding values for AMPA were 92.4% (RSD <2%) at Kirchberg, 98.1% (RSD <2%) at Pixendorf and 69.9% (RSD <4%) at Phyra. The limits of detection for glyphosate were 6.8 μg kg^?1(RSD <10%) at Kirchberg, 4.3 μg kg^?1 (RSD <10%) at Pixendorf, and 46.5 μg kg^?1 (RSD <7%) at Phyra. The limits of detection for AMPA were 26.7 μg kg^?1 (RSD <10%) at Kirchberg, 25.2 μg kg^?1 (RSD <10%) at Pixendorf, and 120.3 μg kg^?1 (RSD <9%) at Phyra. Accordingly, the limits of quantification were 22.7 μg kg^?1(RSD <5%) for glyphosate, and 88.9 μg kg^?1 (RSD <2%) for AMPA at Kirchberg and respectively 14.4 μg kg^?1 (RSD <6%) and 84 μg kg^?1 (RSD <5%) at Pixendorf and 13.8 μg kg^?1 (RSD <6%) and 87.2 μg kg^?1 (RSD <8%) at Phyra. Both substances in the soils were lower than the LOQ before applying the herbicide Roundup. The influence of higher contents of iron oxides, clay, and acidic pH, resulting in a more pronounced adsorption of glyphosate and AMPA in the soils of Phyra and Kirchberg, is demonstrated.     

Multi-Residue Analysis of Herbicides in Soil with an UPLC-ESI-MS Method

A rapid and sensitive method was developed for the determination of 51 herbicides in soil by ultra-performance liquid chromatography-electrospray ionization-mass spectrometry (UPLC–ESI–MS). Using acetonitrile effectively extracted 22 kinds of triazine and other basic herbicides, and using 90:10 v/v acetonitrile-phosphate buffer (pH = 7.5) effectively extracted another 29 herbicides. The extract has not cleaned up further. Chromatographic separation was achieved within 10 min using gradient elution with acetonitrile–water as a mobile phase for 22 triazine and phenylurea herbicides, and with 5 mM ammonium acetate containing 0.1% formic acid aqueous solution–acetonitrile as a mobile phase for another 29 herbicides. The response was linear over two orders of magnitude with correlation coefficients (r²) higher than 0.99. The limits of quantification for the herbicides varied from 0.2 to 20 µg kg^?1. The intra- and inter-day precisions (relative standard deviation, RSD) were 2.2–9.3% and 5.7–17.1%, respectively. The average recovery varied from 61.6 to 112% with the RSD of 1.6–11.3%. Analyzing 51 soil samples from 17 counties formed the basis of this method. Three herbicide residues were found in four counties. Atrazine residue in soil for 17 counties was found; its content was 0.4–9.8 μg kg^?1. Nicosulfuron residue in soil for two counties was found, with a high up to 133 or 1317 μg kg^?1. Propazine (0.3 and 1.34 μg kg^?1), atratone (2.14 and 3.93 μg kg^?1), and cynanazine (0.34 μg kg^?1) in soils for some counties were also found. The validated method can ensure the rapid multi-class, multi-residue analysis at low μg kg^?1 level for 47 herbicides in soil. The developed method provides an effective analytical basis for controlling herbicide dosage, investigating their distribution and degradation, and evaluating their hazards on the environment and human health.     

Quantification of nitrophenols,chlorophenols, and hexachlorocyclohexanes in agricultural soils in the vicinity of industrial area for the assessment of human health hazard and risk

In this study, quantification of nitrophenol (NP), chlorophenol (CP), and hexachlorocyclohexane (HCH) compounds in agricultural soils in the vicinity of the industrial region in northern Uttar Pradesh, India was carried out for the assessment of human health hazard. The concentration of ∑NP, ∑CP, and ∑HCH compounds ranged 0.33–3.64 mg kg^?1, 0.06–3.18 μg kg^?1, and 1.23–17.24 mg kg^?1, respectively, and were within the soil quality guidelines for the protection of human and environment health. Human health hazard index and cancer risk, on the basis of average daily intake of these compounds through soil for human adults and children, was lower than the acceptable limit. This study suggested low health hazard and risk due to phenolic and HCH compounds to human population.     

Concentration,Distribution, Source,and Risk Assessment of PAHs and Heavy Metals in Surface Water from the Three Gorges Reservoir,China

Fifteen polycyclic aromatic hydrocarbons (PAHs) and heavy metals (Cr, Ni, As, Cd, Pb, and Hg) were quantified in 19 surface water sites of the Three Gorges Reservoir, China. The total concentrations of 15 PAHs and six heavy metals in the 19 sample sites ranged from 130.8 ng L^?1 to 227.5 ng L^?1 and 3.2 μg L^?1 to 6.0 μg L^?1, respectively. The mean concentration of As was the highest among the six heavy metals (2.1 ± 0.3 μg L^?1), followed by Cr (0.5 ± 0.3 μg L^?1), Ni (1.3 ± 0.1 μg L^?1), Cd (0.2 ± 0.01 μg L^?1), Pb (0.07 ± 0.08 μ g L^?1) and Hg (0.05 ± 0.08 μg L^?1). The isomer ratio results suggest that PAHs at most sites were mainly from petroleum combustion, while coal and biomass combustion was the main source at sites 1, 2, 6, 7, 9, 14, and 17. Based on principal component analysis, the main source of heavy metals was anthropogenic activities and weathering of bedrocks. Depending on characteristic of RQ_(NCs) ≥ 1 and RQ_(MPCs) < 1, BaA showed higher potential ecological risk than other PAHs, therefore, all sampling site needed to be paid much more attention, included some remedial actions. Meanwhile, after assessing human health risk of heavy metal, it was unlikely to experience adverse health effects, even exposing through more pathways and six kinds of heavy metals simultaneously.     

Bioaccessibility-Based Risk Assessment of PAHs in Soils from Sites of Different Anthropogenic Activities in Lagos,Nigeria Using the Fed Organic Estimation Human Simulation Test Method

The aim of this study was to carry out a bioaccessibility-based risk assessment of polycyclic aromatic hydrocarbons (PAHs) in soils from sites of different anthropogenic activities in Lagos, Nigeria. Using an in vitro gastrointestinal model—Fed Organic Estimation Human Simulation Test method (FOREShT), the concentration of bioaccessible 16 priority US Environmental Protection Agency (USEPA) PAHs in soils were determined. Total concentration of 16 priority USEPA PAHs was also determined. The concentration range was 702–253,922 ng g^?1 and 92–760 ng g^?1 for total and bioaccessible PAHs, respectively. For persons involved with activities at these sites no health risks were observed, based on bioaccessibility values of PAHs. Mean daily intake of PAHs from these soils were below the oral mean daily intake threshold for PAHs in food. Also, overall estimated theoretical cancer risk (2.5 × 10^?09, 6.5 × 10^?07, 5.5 × 10^?10, 2.7 × 10^?09, 6.5 × 10^?10, 9.5 × 10^?10, 2.0 × 10^?09, and 4.1 × 10^?07 for the eight sites based on their bioaccessible concentration) for exposure to PAHs in surface soils were below the health guidelines for extreme (1 × 10^?04) and normal (1 × 10^?06) exposures.     

Nutrient Removal as a Function of Corn Stover Cutting Height and Cob Harvest

One-pass harvest equipment has been developed to collect corn (Zea mays L.) grain, stover, and cobs that can be used as bioenergy feedstock. Nutrients removed in these feedstocks have soil fertility implication and affect feedstock quality. The study objectives were to quantify nutrient concentrations and potential removal as a function of cutting height, plant organ, and physiological stage. Plant samples were collected in 10-cm increments at seven diverse geographic locations at two maturities and analyzed for multiple elements. At grain harvest, nutrient concentration averaged 5.5 g?N kg^?1, 0.5 g?P kg^?1, and 6.2 g?K kg^?1 in cobs, 7.5 g?N kg^?1, 1.2 g?P kg^?1, and 8.7 g?K kg^?1 in the above-ear stover fraction, and 6.4 g?N kg^?1, 1.0 g?P kg^?1, and 10.7 g?K kg^?1 in the below-ear stover fraction (stover fractions exclude cobs). The average collective cost to replace N, P, and K was $11.66 Mg^?1 for cobs, $17.59 Mg^?1 for above-ear stover, and $18.11 Mg^?1 for below-ear stover. If 3 Mg ha^?1 of above-ear stover fraction plus 1 Mg of cobs are harvested, an average N, P, and K replacement cost was estimated at $64 ha^?1. Collecting cobs or above-ear stover fraction may provide a higher quality feedstock while removing fewer nutrients compared to whole stover removal. This information will enable producers to balance soil fertility by adjusting fertilizer rates and to sustain soil quality by predicting C removal for different harvest scenarios. It also provides elemental information to the bioenergy industry.     

Assessment of the Genotoxic Potential of Sediments Contaminated with POPs and Agricultural Soils Using Vicia faba Micronucleus Assay

The aim of this study was to assess the levels of some persistent organic pollutants in the surface sediments from the Zahuapan and Atoyac rivers (Tlaxcala, Mexico), as well as to determine the genotoxic potential, by the micronucleus test in Vicia faba, of the sediments and agricultural soils irrigated with water from these rivers. This document is the first study on the presence of POPs in surface sediments of the above-mentioned rivers; among the compounds analyzed are the HCH isomers, DDT and its metabolite DDE, HCB, mirex, aldrin, and 41 PCB congeners. The concentrations of HCB, ΣDDTs, ΣHCHs, and ΣPCBs ranged from 138–510, 45–450, 3–27, and 59–1876 μg kg^?1 dry weight, respectively. The highest levels of HCB, HCH isomers, and PCB congeners were found in the Atoyac River, and these compounds have the potential for causing an environmental impact. On the other hand, biological testing shows that both sediments and agricultural soils possess a genotoxic potential, given that the micronuclei frequency in V. faba is increased.     

Characterization,source apportionment,and human health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in road dust of a small island state in the Caribbean

Sixty-four and fifty-six road dust samples were collected over two seasons from various locations throughout the island of Trinidad and analyzed for the 16 priority PAHs. Total PAH concentrations ranged from 21 ng g^?1 to 4723 ng g^?1 (d.w.) for the rainy season and 36 ng g^?1 to 2428 ng g^?1 (d.w.) for the dry season. The Σ4–6 ring PAHs accounted for 88% and 63% of the 16 PAHs in road dust samples for the rainy and dry seasons, respectively. PAH diagnostic ratios, principal component analysis, and cluster analysis revealed both pyrogenic and petrogenic sources in road dust for the two seasons, with major contributions from vehicular emissions. Contributions from incomplete combustion and petroleum sources were also identified. The estimated Incremental Lifetime Cancer Risk (ILCR) associated with exposure to road dust PAHs in Trinidad for the rainy and dry seasons indicated no potential risk for both children and adults, as denoted by ILCR values lower than 10^?6.     

Phytoextraction of Risk Elements by Willow and Poplar Trees

To characterize the phytoextraction efficiency of two clones of willow trees (Salix x smithiana Willd., Salix rubens) and two clones of poplar trees (Populus nigra x maximowiczii, Populus nigra Wolterson) were planted in contaminated soil (0.4–2.0 mg Cd.kg^?1, 78–313 mg Zn.kg^?1, 21.3–118 mg Cu.kg^?1). Field experiment was carried out in Czech Republic. The study investigated their ability to accumulate heavy metals (Cd, Zn, and Cu) in harvestable plant parts. The poplars produced higher amount of biomass than willows. Both Salix clones accumulated higher amount of Cd, Zn and Cu in their biomass (maximum 6.8 mg Cd.kg^?1, 909 mg Zn.kg^?1, and 17.7 mg Cu.kg^?1) compared to Populus clones (maximum 2.06 mg Cd.kg^?1, 463 mg Zn.kg^?1, and 11.8 mg Cu.kg^?1). There were no significant differences between clones of individual species. BCs for Cd and Zn were greater than 1 (the highest in willow leaves). BCs values of Cu were very low. These results indicate that Salix is more suitable plant for phytoextraction of Cd and Zn than Populus. The Cu phytoextraction potential of Salix and Populus trees was not confirmed in this experiment due to low soil availability of this element.     

Exposure to aflatoxin B<Subscript>1</Subscript> in Thailand by consumption of brown and color rice

This study assessed the aflatoxin B₁ (AFB₁) intake of the Thai population through consumption of contaminated brown and color rice. A total of 240 rice samples from two harvesting periods were collected in June/July 2012 (period I) and in December 2012/January 2013 (period II) and analyzed for AFB₁ by HPLC with fluorescence detection (limit of detection (LOD)?=?0.093 ng/g). Exposure assessment was based on AFB₁ levels in rice and food intake data for rice according to Thai National Consumption. Frequency and levels of AFB₁ were higher in period I (59 %, <LOD?=?26.61 μg kg^?1) than in period II (10 %, <LOD?=?3.51 μg kg^?1). Only one sample exceeded the Thai standard limit for total aflatoxin of 20 μg kg^?1, but 12 out of 240 rice samples exceeded the European Union maximum level for AFB₁ of 2 μg kg^?1. The data showed that the quality and safety of Thai rice largely comply with the requirement for both exports and domestic consumption. According to the Thai National Consumption data, the estimated AFB₁ intake via rice consumption in period I and period II was 0.80 and 0.12 μg kg^?1 bw day^?1, respectively. The potential risk for cancer, based on the recommendation of the JECFA, was estimated to be 0.011 person/year/100,000 people at a mean consumption. Although the risk via consumption of Thai rice seems to be low, the maximum levels of AFB₁ in this staple food suggest that careful monitoring and surveillance of AFB₁ contamination in rice is essential to ensure the safety of rice.     

Hepatosplenomegaly and phytotoxicity of a planktonic cyanobacterium Nostoc sp. BHU001 isolated from agricultural pond

Nostoc sp. BHU001, a planktonic cyanobacterium isolated from an agricultural pond in India, was examined for its toxicity. Mice, administered intraperitoneally with Nostoc sp. BHU001 crude extract (50 mg kg^?1 body weight) died at 4.5 h. Examination of liver and spleen showed microcystin (MC)-like symptoms. Serum enzyme aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities increased by 1.6–1.8 and 2.6–3.0-folds, respectively at 50 and 100 mg crude extract kg^?1 body weight. Thin layer chromatography of the crude extract produced five bands (N-1 to N-5). UV absorption maxima of band N-4 corresponded to that of standard microcystin-LR. Further analysis of the band N-4 by high-performance liquid chromatography gave a retention time (R _t ) of 4.61 min similar to that of standard microcystin–LR (LR stands for lysine and arginine). Total MC content was quantified by enzyme-linked immunosorbent assay, and was 189.9 μg g^?1 of crude extract, 9.8 μg l^?1 of spent medium and 5.5 μg l^?1 of pond water. Exposure of rice (Oryza sativa var. Sonam) seeds to the crude extract did not affect their germination, but inhibited the root and shoot growth of seedlings by 27.3 and 42.89 folds at 3 mg ml^?1 crude extract, respectively.     

Distribution,sources, and health risk assessment of polycyclic aromatic hydrocarbons in dust from urban environment in the Niger Delta,Nigeria

The concentrations of the 16 U.S. Environmental Protection Agency polycyclic aromatic hydrocarbons (PAHs) were measured in urban street dust with a view to understanding the potential risk to urban residents exposed to street dust, sources, and distribution of the PAHs. Gas chromatography–mass spectrometry was used to measure the concentrations of the PAHs after ultra-sonication with hexane/dichloromethane and clean up. The total concentrations of the ?16 PAHs in the urban street dust from Warri and its environs ranged from 165.1 to 1012 µg kg^?1. The isomeric ratios and the PCA indicated that combustion of petroleum and biomass are the major sources of PAHs in Warri and its environs. The total BaP carcinogenic and mutagenic potency concentrations (?BaP_TEQ and ?BaP_MEQ) were in the range of 0.03 to 219 µg kg^?1 and 0.52 to 182 µg kg^?1, respectively. The incremental life cancer risk from exposure of the residents of Warri and its environs ranged from 4.07 × 10^?7 to 3.11 × 10^?3 and 2.13 × 10^?7 to 1.49 × 10^?3 for the children and adults, respectively, which were higher than the baseline value of acceptable risk of 10^?6 (i.e., one case per million people).     

Effect of Intravenous Infusion of Dexmedetomidine Combined with Inhalation of Isoflurane on Arterial Oxygenation and Intrapulmonary Shunt During Single-Lung Ventilation

To investigate the changes in arterial oxygenation and intrapulmonary shunt during one-lung ventilation (OLV) with intravenous infusion of dexmedetomidine combined with isoflurane inhalation. ASA I–II 60 patients aged 18–70 year, undergoing OLV during elective thoracic surgery were randomly allocated to two groups: (1) isoflurane + saline (group NISO, n = 30) and (2) isoflurane + dexmedetomidine (group DISO, n = 30). After induction, anesthesia was maintained with intravenous infusion of remifentanil 0.1–0.2 μg kg^?1 min^?1 and inhalation isoflurane (1.0–2.0 %). In addition, anesthesia was maintained with intravenous infusion of dexmedetomidine 0.7 μg kg^?1 h^?1 in DISO group and saline 0.25 ml kg^?1 h^?1 in NISO group. Bispectral Index values were maintained within 40–60 by changing the concentration of isoflurane in all groups. Arterial blood gas samples and central venous blood gas samples were taken as follows: during two-lung ventilation before OLV and during the first 40 min of OLV. 45 Patients completed the study, with 23 patients in DISO group and 22 patients in NISO group. The two groups were comparable in terms of demographic variables, hemodynamic, PaO₂, Qs/Q_T, end expiration isoflurane and BIS levels during the operation. Compared with patients in the group NISO, there were significant increases with PaO₂, significant decrease with Qs/Q_T, significant decrease with end expiration isoflurane, and significant decrease with HR in the group DISO during the first 40 min of OLV (P < 0.05). Dexmedetomidine infusions decrease the requirement for isoflurane, decrease intrapulmonary shunt, and moderate the change in PaO₂ and may be useful in managing OLV.     

Hyperaccumulator Oilcake Manure as an Alternative for Chelate-Induced Phytoremediation of Heavy Metals Contaminated Alluvial Soils

The ability of hyperaccumulator oilcake manure as compared to chelates was investigated by growing Calendula officinalis L for phytoremediation of cadmium and lead contaminated alluvial soil. The combinatorial treatment T₆ [2.5 g kg^?1oilcake manure + 5 mmol kg^?1 EDDS] caused maximum cadmium accumulation in root, shoot and flower up to 5.46, 4.74 and 1.37 mg kg^?1and lead accumulation up to 16.11, 13.44 and 3.17 mg kg^?1, respectively at Naini dump site, Allahabad (S₃). The treatment showed maximum remediation efficiency for Cd (RR = 0.676%) and Pb (RR = 0.202%) at Mumfordganj contaminated site (S₂). However, the above parameters were also observed at par with the treatment T₅ [2.5 g kg^?1oilcake manure +2 g kg^?1 humic acid]. Applied EDDS altered chlorophyll–a, chlorophyll–b, and carotene contents of plants while application of oilcake manure enhanced their contents in plant by 3.73–8.65%, 5.81–17.65%, and 7.04–17.19%, respectively. The authors conclude that Calendula officinalis L has potential to be safely grown in moderately Cd and Pb-contaminated soils and application of hyperaccumulator oilcake manure boosts the photosynthetic pigments of the plant, leading to enhanced clean-up of the cadmium and lead-contaminated soils. Hence, the hyperaccumulator oilcake manure should be preferred over chelates for sustainable phytoremediation through soil-plant rhizospheric process.     

Polycyclic aromatic hydrocarbons (PAHs) in the environment of Beijing,China: Levels,distribution, trends and sources

Polycyclic aromatic hydrocarbons (PAHs) have become a major type of persistent organic pollutant (POPs) in the world. To well understand the occurrence, spatial distribution and source apportionment of 16 PAHs in different media in Beijing, a comprehensive study was conducted based on 337 obtained and subsequently selected samples in four specific media, including soil, road dust, surface water and atmosphere covering sampling time spanning from 2005 to 2014. Mean concentrations of Σ16 PAHs in soils (878.5 μg/kg) decreased from inner city to exterior areas with different land uses decreased in the order of industrial estate (2510 μg/kg)>educational area (1331 μg/kg)>Park (783 μg/kg)>cultivated (650 μg/kg)>roadside (583 μg/kg)>residential (568 μg/kg)>green area (478 μg/kg)>forest area (125 μg/kg). Meanwhile, PAHs concentrations in branch roads were slightly higher than trunk roads and mainly concentrated in urban areas (1136 μg/kg). Affected by industrial and residential areas, PAHs concentrations in downstream surface rivers were much higher than upstream surface rivers (475 ng/L). Due to strong mobility, PAHs concentrations in atmosphere were not equally distributed around the study area (157.59 ng/m³). The result of source apportionment determined by diagnostic ratios method indicated PAHs in multiple media in Beijing are mainly from coal and biomass combustion.     

Mycotoxigenic fungi and mycotoxins associated with stored maize from different regions of Lesotho

Samples of stored maize from villages located in five different agroecological zones (southern lowlands, northern lowlands, Senqu river valley, foothills and mountains) of Lesotho were collected in 2009/10 and 2010/11 and assessed for contamination with toxigenic fungi. The water activity of all samples collected during the two seasons was <0.70. The total fungal populations of the maize from different regions in the two seasons was not significantly different (p?>?0.05). Fusarium verticillioides, F. proliferatum and F. subglutinans predominated in different regions in both seasons based on molecular analyses. In the 2009/10 season, the isolates of these species all produced FB₁, while in the 2010/11 season, very few produced FB₁. A. flavus isolates (2009/10) were recovered from mountains and Senqu river valley samples while the 2010/11 isolates were predominantly from the foothills and northern lowlands. The mountain isolates of Aspergillus section Flavi produced the highest levels of AFB₁ (20 mg kg^?1). Aspergillus parasiticus was only isolated from the foothills, Senqu river valley and southern lowlands samples, and the AFB₁ levels produced ranged from ‘none detected’ to 3.5 mg kg^?1. The Aspergillus ochraceous isolates were least frequently encountered in both seasons. In the 2009/10 season, the isolates from the northern lowlands produced ochratoxin A (OTA) in culture. No isolates of A. niger from different regions in both seasons produced any OTA. Multi-mycotoxin analyses of the maize samples were done for a range of mycotoxins. At least one sample from each region in both seasons was FB₁-positive. FB₁ levels for 2010/11 samples (7–936 μg kg^?1) were higher than in the 2009/10 season (2–3 μg kg^?1). In both seasons, the mountains registered the highest levels of FB₁. Deoxynivalenol (DON) was recovered from all the samples analysed, with the highest mean contamination of 1,469 μg kg^?1 in samples from the northern lowlands. Moniliformin (MON) was detected from all agroecological zones in the two seasons (5–320 μg kg^?1 in 2009/10; 15–1,205 μg kg^?1 in 2010/11). Emerging toxins such as fusaproliferin (FUS) and beauvericin (BEA) were also detected. OTA was not detected in any of the samples analysed. Only one 2009/10 sample in the Senqu river valley was positive for AFB₁. This is the first report on toxigenic fungi and multi-mycotoxin contamination of maize samples from subsistence farmers’ stores in different agroecological zones of Lesotho.