Anhydrosugar and sugar alcohol organic markers associated with carboxylic acids in particulate matter from incense burning

Aerosol from the burning two types of sandalwood-based incense, Hsing Shan and Lao Shan, was analyzed to characterize the chemical profile of total particulate matter emitted. The total particulate matter (PM) mass emission factors were 46.3 ± 2.68 mg g^?1 of Hsing Shan incense and 43.7 ± 1.08 mg g^?1 of Lao Shan incense. Chemical analysis of emissions from the two types of incense revealed that of the 25 components in four groups characterized, anhydrosugars formed the major group, at 46.7–52.2% w/w of the identified particulate and 1078.3–1169.8 μg g^?1 of incense, followed by inorganic salts at 30.4–31.8% w/w of identified particulate and 681.6–734.0 μg g^?1 of incense, carboxylic acids at 12.0–17.1% w/w of the identified particulate and 268.6–392.8 μg g^?1 of incense, and sugar alcohols at 4.44–5.38% w/w of the identified particulate and 102.3–120.6 μg g^?1 of incense. More anhydrosugars and sugar alcohols were emitted from Lao Shan incense than from Hsing Shan incense whereas more carboxylic acids and organic salts were emitted from Hsing Shan than from Lao Shan. These differences were due to structural and functional differences in the young sandalwood used to make Hsing Shan and the aged sandalwood used to make Lao Shan. The anhydrosugar levoglucosan, used as a marker of biomass burning, was always the most abundant species in emitted PM for both incenses (Lao Shan 21.7 mg g^?1 of PM and Hsing Shan 18.7 mg g^?1). K⁺ and Cl^? were the second most abundant components (K⁺ and Cl^? were summed), accounting for 10.6 mg g^?1 of Hsing Shan PM and 9.85 mg g^?1 of Lao Shan PM. The most abundant carboxylic acids in the emissions were formic, acetic, succinic, glutaric and phthalic acid. The latter is a fragrance ingredient and a potential health hazard and was twice as prevalent in Lao Shan emissions. Xylitol was the most prevalent of the sugar alcohols at 35.7–36.6% w/w of total identified sugar alcohols. These abundant species are potential markers for incense burning. K⁺, levoglucosan, mannosan and xylitol are already reported in discriminator ratios for wood burning and it is proposed here that these can and should also apply to incense burning. The calculated discriminator ratios for two types of incense burning reported here are 0.229–0.288 for K/Levo, 12.5–13.5 for Levo/Manno, and 21.5–23.7 for the novel discriminator ratio Levo/Xylitol.     

Bioaccumulation and uptake routes of perfluoroalkyl acids in Daphnia magna

Perfluoroalkyl acids (PFAs), one kind of emerging contaminants, have attracted great attentions in recent years. However, the study about their bioaccumulation mechanism remains scarce. In this research, the bioaccumulation of six kinds of PFAs in water flea Daphnia magna was studied. The uptake rates of PFAs in D. magna ranged from 178 to 1338 L kg^?1 d^?1, and they increased with increasing perfluoroalkyl chain length; the elimination rates ranged from 0.98 to 2.82 d^?1. The bioaccumulation factors (BAFs) of PFAs ranged from 91 to 380 L kg^?1 in wet weight after 25 d exposure; they increased with increasing perfluoroalkyl chain length and had a significant positive correlation with the n-octanol/water partition coefficients (log K_ow) of PFAs (p < 0.05). This indicated that the hydrophobicity of PFAs plays an important role in their bioaccumulation. The BAFs almost kept constant when the PFA concentrations in aqueous phase increased from 1 to 10 μg L^?1. Scenedesmus subspicatus, as the food of D. magna, did not significantly affect the bioaccumulation of PFAs by D. magna. Furthermore, the body burden of PFAs in the dead D. magna was 1.08–2.52 times higher than that in the living ones, inferring that the body surface sorption is a main uptake route of PFAs in D. magna. This study suggested that the bioaccumulation of PFAs in D. magna is mainly controlled by their partition between organisms and water; further research should be conducted to study the intrinsic mechanisms, especially the roles of protein and lipid in organisms.     

Assessment of plant-driven uptake and translocation of clofibric acid by Scirpus validus

Pharmaceutical compounds are now considered as emerging contaminants of environmental concern. The overall objective of this study was to evaluate the uptake and translocation of clofibric acid (CA) by the macrophyte Scirpus validus growing hydroponically. A set of the three replicates was established for each exposure time and for each CA concentration. Plants were grown in 4 L vessels (four plants per vessel corresponding to the three exposure period studies, i.e., 7, 14, 18, and 21 days) which contained an aerated modified Hoagland nutrient solution that was spiked with CA at concentrations of 0.5, 1.0, and 2.0 mg?L^?1. At each exposure period, CA concentration was measured in the nutrient solutions. A sea sand disruption method was employed for the extraction of CA from plant tissues. The determination of the pharmaceutical concentration was carried out using solid phase extraction (SPE) followed by chromatographic analysis. The quantification of CA concentrations in both nutrient solutions (after SPE) and plant tissues (after extraction) was conducted by chromatographic analysis. CA concentrations of 5.4–26.8 μg?g^?1 (fresh weight) were detected in the roots and 7.2–34.6 μg?g^?1 (fresh weight) in the shoots after 21 days. Mass balance calculations showed that S. validus uptake alone accounted for a significant contribution (6–13 % for the roots and 22–49 % for the shoots) of the total loss of CA. The bioaccumulation factors (BAFs) based on fresh weight for the roots ranged from 6.6 to 23.2, while values for the shoots ranged from 9.5 to 32.1. All the BAFs for the shoots were greater than those in the roots, implying that CA has greater tendency to be translocated to the shoots, rather than the roots of S. validus. All the shoot-to-root concentration ratios were more than 1, denoting that the shoots of S. validus do preferentially accumulate CA. We demonstrated that CA can be actively taken up, subsequently translocated and accumulated by aboveground tissues of S. validus. Since S. validus could account for the removal of 28–62 % of the total mass loss of CA from the system, such phytoremediation technology has great potential for the removal of pharmaceuticals such as CA from inflowing waters.     

Exposure of German residents to ethylene and propylene glycol ethers in general and after cleaning scenarios

Glycol ethers are a class of semi-volatile substances used as solvents in a variety of consumer products like cleaning agents, paints, cosmetics as well as chemical intermediates.We determined 11 metabolites of ethylene and propylene glycol ethers in 44 urine samples of German residents (background level study) and in urine samples of individuals after exposure to glycol ethers during cleaning activities (exposure study).In the study on the background exposure, methoxyacetic acid and phenoxyacetic acid (PhAA) could be detected in each urine sample with median (95th percentile) values of 0.11 mg L^?1 (0.30 mg L^?1) and 0.80 mg L^?1 (23.6 mg L^?1), respectively. The other metabolites were found in a limited number of samples or in none.In the exposure study, 5–8 rooms were cleaned with a cleaner containing ethylene glycol monobutyl ether (EGBE), propylene glycol monobutyl ether (PGBE), or ethylene glycol monopropyl ether (EGPE). During cleaning the mean levels in the indoor air were 7.5 mg m^?3 (EGBE), 3.0 mg m^?3 (PGBE), and 3.3 mg m^?3 (EGPE), respectively. The related metabolite levels analysed in the urine of the residents of the rooms at the day of cleaning were 2.4 mg L^?1 for butoxyacetic acid, 0.06 mg L^?1 for 2-butoxypropionic acid, and 2.3 mg L^?1 for n-propoxyacetic acid.Overall, our study indicates that the exposure of the population to glycol ethers is generally low, with the exception of PhAA. Moreover, the results of the cleaning scenarios demonstrate that the use of indoor cleaning agents containing glycol ethers can lead to a detectable internal exposure of residents.     

Preliminary data suggest that venlafaxine environmental concentrations could be toxic to plants

Venlafaxine hydrochloride is a structurally novel antidepressant. Its occurrence in surface waters and drinking water has only been reported in recent works. The aim of this work is to assess the acute and chronic sublethal toxicity of venlafaxine in relevant taxa of riparian ecosystems. We used the fern Polystichum setiferum during the critical life stage of development. Reliable biomarkers of cell viability (mitochondrial activity), plant physiology (chlorophyll), and growth (DNA content) were assessed as sensitive endpoints of toxicity. About DNA quantification, our results show that venlafaxine induces acute lethal phytotoxicity at 24 and 48 h (LOECs 1 μg L^?1 and 0.1 μg L^?1, respectively). At 24 h, hormetic effects in spores of P. setiferum mitochondrial activity mask lethality and adverse effects are observed (LOEC 1 μg L^?1). At 48 h a reduction in the mitochondrial activity happens (LOEC 10 μg L^?1). In chronic exposure of 1 week, LOEC for DNA is 0.1 μg L^?1. Mitochondrial activity showed a strong hormetic stimulation of a surviving spore population (LOEC 10 μg L^?1). Changes were not observed in chlorophyll autofluorescence. Environmental concentrations of venlafaxine can be deleterious for the development of significant populations of sensitive individuals in riparian ecosystems.     

Simultaneous reduction of Cr(VI) and oxidation of As(III) by Bacillus firmus TE7 isolated from tannery effluent

Hexavalent chromium [Cr(VI)] and arsenite [As(III)] are the most toxic forms of chromium and arsenic respectively, and reduction of Cr(VI) to Cr(III) and oxidation of As(III) to As(V) has great environmental implications as they affect toxicity and mobility of these toxic species. Bacillus firmus strain TE7, resistant to chromium and arsenic was isolated from tannery effluent. The strain exhibited ability to reduce Cr(VI) and oxidize As(III). It reduced 100 mg L^?1 Cr(VI) within 60 h in nutrient broth and oxidized 150 mg L^?1 As(III) within 10 h in minimal medium. It also completely reduced 15 mg L^?1 Cr(VI) and oxidized 50 mg L^?1 of As(III) simultaneously in minimal medium. To the best of our knowledge, this is the first bacterial strain showing simultaneous reduction of Cr(VI) and oxidation of As(III) and is a potential candidate for bioremediation of environments contaminated with these toxic metal species.     

Immunoassays as high-throughput tools: Monitoring spatial and temporal variations of carbamazepine,caffeine and cetirizine in surface and wastewaters

Carbamazepine (CBZ), caffeine and cetirizine were monitored by enzyme-linked immunosorbent assays (ELISAs) in surface and wastewaters from Berlin, Germany. This fast and cost-efficient method enabled to assess the spatial and temporal variation of these anthropogenic markers in a high-throughput screening. CBZ and cetirizine were detected by the same antibody, which selectively discriminates between both compounds depending on the pH value used in the incubation step. To our best knowledge, this is the first dual-analyte immunoassay working with a single antibody.The frequent sampling with 487 samples being processed allowed for the repeated detection of unusually high concentrations of CBZ and caffeine. ELISA results correlate well with the ones obtained by liquid chromatography tandem mass spectrometry (LC-MS/MS). Caffeine concentrations found in surface waters were elevated by combined sewer overflows after stormwater events. During the hay fever season, the concentrations of the antihistamine drug cetirizine increased in both surface and wastewaters.Caffeine was almost completely removed during wastewater treatment, while CBZ and cetirizine were found to be more persistent. The maximum concentrations of caffeine, CBZ and cetirizine found in influent wastewater by LC–MS/MS were 470, 5.0 and 0.49 μg L⁻¹, while in effluent wastewater the concentrations were 0.22, 4.5 and 0.51 μg L⁻¹, respectively. For surface waters, concentrations up to 3.3, 4.5 and 0.72 μg L⁻¹ were found, respectively.     

Chlorpyrifos-induced changes in oxidant/antioxidant status and haematological parameters of Cyprinus carpio carpio: Ameliorative effect of lycopene

The present study was carried out to investigate the potential ameliorative effects of lycopene against chlorpyrifos (CPF) toxicity in carp. The fish were divided into 7 different experimental groups and received the following treatments: Group 1, control; Group 2, orally administered corn oil; Group 3, oral lycopene (10 mg kg^?1 body weight); Group 4, exposure to 0.040 mg L^?1 CPF; Group 5, exposure to 0.040 mg L^?1 CPF plus oral administration of 10 mg kg^?1 lycopene; Group 6, exposure to 0.080 mg L^?1 CPF; and Group 7, exposure to 0.040 mg L^?1 CPF plus oral administration of 10 mg kg^?1 lycopene. Treatment was continued for 14 d and samples of the blood and tissue (liver, kidney, and gill) were collected at the end of the experiment and analysed for their oxidant–antioxidant status, including the malondialdehyde (MDA) levels, and the superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px) activity. The samples were also measured for changes in the haematological parameters, such as the red blood cell (RBC) and white blood cell (WBC) counts, the haemoglobin concentration (Hb), the haematocrit (Ht) level, and the erythrocyte indices: the mean corpuscular volume (MCV), the mean corpuscular haemoglobin (MCH) and the mean corpuscular haemoglobin concentration (MCHC). The findings of this study demonstrated that CPF had a negative effect on the haematological parameters and the antioxidant enzyme activities of the fish; this toxic effect was neutralised by the administration of lycopene. The present results suggest that lycopene (10 mg kg^?1) can be effective in the protection of CPF-induced toxicity in fish.     

The effects of antibiotic cocktails at environmentally relevant concentrations on the community composition and acetate biodegradation kinetics of bacterial biofilms

Antibiotics and antibacterials are present in water bodies worldwide but little is known about their effects on the biological processes often used to treat water. In this research, the effect of antibiotics on bacterial activity and community structure was investigated by growing biofilms in the presence and absence of a mixture of three compounds (sulfamethoxazole, erythromycin, and ciprofloxacin) in a continuous-flow rotating annular bioreactor fed acetate as a carbon and energy source. Steady-state, surface area-normalized substrate utilization rates for all antibiotic treatments (all at 0.33 μg L^?1, all at 3.33 μg L^?1, and 1 at 3.33 μg L^?1 with the other 2 at 0.33 μg L^?1) were similar to the control experiments. Higher attached biomass levels in the experiments with ciprofloxacin at 3.33 μg L^?1 resulted in lower steady-state biomass-normalized substrate utilization rates in comparison to other runs. Microbial community analyses via automated ribosomal intergenic spacer analysis revealed significant shifts in community structure for the experiments dosed with the highest concentrations of ciprofloxacin, suggesting that the antibiotic selected for more resistant bacterial strains. The results of this research also suggest that mixtures of antibiotics at the sub-μg L^?1 concentrations typically observed in surface waters are unlikely to affect biological process performance, at least in terms of the degradation of easily assimilable compounds. Conversely, changes to community structure and biofilm quantity might be expected with ciprofloxacin at μg L^?1 concentrations.     

Polychlorinated biphenyls hot and cold seasons distribution in see water,sediment, and fish samples in the Khour-e-Mousa (Mah-Shahr), Iran

The concentrations of polychlorinated biphenyls (PCBs) were assessed at four sites in Khour-e-Mousa (Mah-Shahr), Iran. Sea water, sediment and fish (cynoglossus bilineatus) samples were taken at each site and were analysed for PCB levels. To investigate the possible source of PCBs found in fish samples, sediments and waters were collected from four sites (D1, D2, D3, and D4) and studied. The relationship between PCB concentrations in sediment, water and fish is discussed. The results indicate that PCBs are detected in all fish samples and its concentration range from 3.2 to 102.7 μg kg^?1 dry weight and 5.4–149.7 μg kg^?1 dry weight in cold and warm seasons, respectively. The D2 and D4 sites were found to have the highest and lowest levels of PCB concentrations, respectively. Total congener PCB (CB, 28, 52, 44, 101, 149, 118, 153, 138, and 180) concentrations at the sediment samples for D1, D2, D3, and D4 sites ranged from 1.6 to 30.9 μg kg^?1 dry weight and 2.3–47.1 μg kg^?1 dry weight in cold and warm seasons, respectively. The total PCB concentrations for D2 site were found to be significantly higher than other three sites. Total water congener PCB (CB, 28, 52, 44, 101, 149, 118, 153, 138, and 180) concentrations ranged from 0.01 to 0.25 μg L^?1 and 0.02–0.39 μg L^?1 in cold and warm seasons, respectively.     

A highly resolved anion-exchange chromatographic method for determination of saccharidic tracers for biomass combustion and primary bio-particles in atmospheric aerosol

An improved high-performance anion-exchange chromatography (HPAEC) with pulsed amperometric detection (PAD) method is developed and validated for simultaneous determination of atmospherically relevant sugar alcohols, monosaccharides, and monosaccharide anhydrides. The improved method enables the separation of levoglucosan and arabitol which were not or insufficiently separated by the previous HPAEC–PAD methods. Reproducibility of the method was tested for both standard solutions and atmospheric aerosol samples. The peak area relative standard deviation (RSD%) of standard solutions were found to be lower than 1.5% for consecutive analyses (n = 3) and lower than 4% for day to day variation (n = 9). The peak area RSD% of atmospheric samples with typical European wintertime monosaccharide concentrations (n = 9) was found to be similar to that of standard solutions. Limits of detection ranged from 0.002 mg L^?1 for inositol to 0.08 mg L^?1 for fructose. The developed method offers a simple, reliable and cost effective determination of atmospheric tracers for biomass combustion and for selected bio-aerosol components at sub-nanogram per cubic-meter-air concentration levels for routine analysis.     

Phytoremedial assessment of flora tolerant to heavy metals in the contaminated soils of an abandoned Pb mine in Central Portugal

Significant accumulation of heavy metals in soils and flora exists around the abandoned Barbadalhos Pb mine in Central Portugal. Soil and plant samples [49 species] were collected from two line transects, LT 1 and LT 2, in the mineralized and non-mineralized area, respectively to gain a comprehensive picture of heavy metals in soils and flora to assess its potential for phytoremediation. Phytosociological inventories of the vegetation were made using the Braun-Blanquet cover-abundance scale. Metal concentrations in soil ranged from (in mg kg^?1): 98–9330 [Pb], 110–517 [Zn], 7.1–50 [Co], 69–123 [Cr], 31–193 [Cu], 33 400–98 500 [Fe], 7.7–51 [Ni], 0.95–13 [Ag], 2.8–208 [As], and 71–2220 [Mn] along LT 1; and 24–93 [Pb], 30–162 [Zn], 3.7–34 [Co], 61–196 [Cr], 21–46 [Cu], 24 100–59 400 [Fe], 17–87 [Ni], 0.71–1.9 [Ag], 4.3–12 [As], and 44–1800 [Mn] along LT 2. Plant metal content ranged from (in mg kg^?1): 1.11–548 [Pb], 7.06–1020 [Zn], 0.08–2.09 [Co], 0.09–2.03 [Cr], 2.63–38.5 [Cu], 10.4–4450 [Fe], 0.38–8.9 [Ni], and 0.03–1.9 [Ag] along LT 1; and 0.94–11.58 [Pb], 2.83–96.5 [Zn], 0.12–1.44 [Co], 0.21–1.49 [Cr], 1.61–22.7 [Cu], 4.6–2050 [Fe], 0.51–4.81 [Ni], and 0.02–0.31 [Ag] along LT 2. Plants with highest uptake of metals were: Cistus salvifolius (548 mg Pb kg^?1), Digitalis purpurea (1017 mg Zn kg^?1 and 4450 mg Fe kg^?1). Mentha suavolens and Ruscus ulmifolius were seen to hyperaccumulate Ag (1.9 and 1 mg Ag kg^?1, respectively). More metals and higher concentrations were traced in plants from LT 1, especially for Pb and Zn.     

Air pollutants in rural homes in Guizhou,China – Concentrations,speciation, and size distribution

Several types of fuels, including coal, fuel wood, and biogas, are commonly used for cooking and heating in Chinese rural households, resulting in indoor air pollution and causing severe health impacts. In this paper, we report a study monitoring multiple pollutants including PM₁₀, PM_2.5, CO, CO₂, and volatile organic compounds (VOCs) from fuel combustion at households in Guizhou province of China. The results showed that most pollutants exhibited large variability for different type of fuels except for CO₂. Among these fuels, wood combustion caused the most serious indoor air pollution, with the highest concentrations of particulate matters (218～417 μg m^?3 for PM₁₀ and 201～304 μg m^?3 for PM_2.5), and higher concentrations of CO (10.8 ± 0.8 mg m^?3) and TVOC (about 466.7 ± 337.9 μg m^?3). Coal combustion also resulted in higher concentrations of particulate matters (220～250 μg m^?3 for PM₁₀ and 170～200 μg m^?3 for PM_2.5), but different levels for CO (respectively 14.5 ± 3.7 mg m^?3 for combustion in brick stove and 5.5 ± 0.7 mg m^?3 for combustion in metal stove) and TVOC (170 mg m^?3 for combustion in brick stove and 700 mg m^?3 for combustion in metal stove). Biogas was the cleanest fuel, which brought about the similar levels of various pollutants with the indoor case of non-combustion, and worth being promoted in more areas. Analysis of the chemical profiles of PM_2.5 indicated that OC and EC were dominant components for all fuels, with the proportions of 30～48%. A high fraction of SO₄^2? (31～34%) was detected for coal combustion. The cumulative percentages of these chemical species were within the range of 0.7～1.3, which was acceptable for the assessment of mass balance.     

Decolorization of azo dye reactive black B by Bacillus cereus strain HJ-1

Reactive black B (RBB) is a group of azo dyes that are widely used in the textile industry. In this study, a new microbial strain was isolated from azo dye contaminated river sediment which is capable of degrading RBB. The strain was identified as Bacillus cereus strain HJ-1 by 16S rRNA gene sequences analysis. The optimal conditions for RBB decolorization by B. cereus strain HJ-1 are: 25 °C, pH 8, 1 CMC of triton X-100, 0.15 g L^?1 of added yeast extract, 0.125 g L^?1 of added glucose and static culture. Then the toxicity of RBB on the green algae Chlorella vulgaris was determined. The results showed that the median effective concentration (EC₅₀) of RBB for C. vulgaris is 48 mg L^?1 and toxicity will really decrease after decolorization. In the end, B. cereus strain HJ-1 was amended into the origin river sediment and analyzed the whole microbial community structure of river sediment samples by PCR-DGGE technique. The result showed that B. cereus strain HJ-1 could survive in the river sediment after 12 d of incubation. Based on this work, we hope that these findings could provide some useful information for applying the decolorization of RBB in our environment.     

Urinary metabolite levels of pyrethroid insecticides in infants living in an agricultural area of the Province of Jiangsu in China

Pyrethroid insecticides are extensively and increasingly applied in agricultural and residential environments in China. Children’s exposure to pesticides attracted global concerns because of their particular vulnerability. Several studies have reported residual pyrethroid levels in urine both in adults and in children. However, few published data focused on very young infants. The study aimed to assess exposure to pyrethroid insecticides in young infants and investigate the potential influence factors on pyrethroid exposure levels. Data on pyrethroids exposure was based on questionnaire items and measurement of urinary metabolite levels among 481 infants. We detected pyrethroid metabolites of 3-phenoxybenzoic acid (3-PBA), cis- and trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid (cis-DCCA and trans-DCCA) in urine using a gas chromatography-mass spectrometry method. Median values for urinary pyrethroid metabolites in these infants were 0.39 μg L^?1 for 3-PBA, 0.18 μg L^?1 for cis-DCCA, 0.92 μg L^?1 for trans-DCCA, respectively. About 60.9% of the infants had urinary concentrations of three pyrethroid metabolites that were above the level of 0.10 μg L^?1 (limit of detection, LOD). These findings of the urinary metabolites were comparable or slightly higher than those children from the other countries. From questionnaire, we learned that more than 70% of households reported that they or family members had applied mosquito repellents in infants. Above data indicated the need to assess the potential adverse effects of pyrethroids exposure on infants in order to take adequate measures to protect them from pesticide exposures during early childhood.     

Responses of antioxidant status and Na+–K+-ATPase activity in gill of rainbow trout,Oncorhynchus mykiss,chronically treated with carbamazepine

In recent years, chemical pollution by the residual pharmaceuticals has been increasingly important issue due to its widely present in the aquatic environment. However, the toxicological effects of residual pharmaceuticals on fish have not been adequately researched. The aim of this work is to investigate the toxic effect of CBZ, an anticonvulsant drug commonly present in aquatic environment, on antioxidant status and Na⁺–K⁺-ATPase in gill of rainbow trout exposed to sublethal CBZ (1.0 μg L⁻¹, 0.2 mg L⁻¹ and 2.0 mg L⁻¹) for 7, 21 and 42 d. After prolonged exposure of CBZ at higher test concentration (0.2 or 2.0 mg L⁻¹), oxidative stress was apparent as reflected by the significant higher LPO and CP levels in fish gill, as well as the significant inhibition of antioxidant enzymes activities including SOD, CAT, GR and GPx. Besides, reduced glutathione level and Na⁺–K⁺-ATPase activity were significantly lower than those of the control after 42 d of exposure to CBZ at higher test concentration (0.2 or 2.0 mg L⁻¹). The results of this study indicate that chronic exposure of CBZ has altered multiple physiological indices in fish gill; however, before those parameters are used as special biomarkers for monitoring residual pharmaceuticals in aquatic environment, more detailed experiments in laboratory need to be performed in the future.     

The relationship of root porosity and radial oxygen loss on arsenic tolerance and uptake in rice grains and straw

The correlations among arsenic (As) accumulation in grains and straw, rates of radial oxygen loss (ROL), and porosity of roots using 25 rice cultivars were investigated based on two pot experiments: (1) soil with addition of 100 mg As kg^?1 for analysis of As in grains and straw, and (2) deoxygenated solution for analyzing rates of ROL and porosity of roots. The results showed that there were great differences in grain As (0.71–1.72 mg kg^?1) and straw As (15.6–31.7 mg kg^?1), rates of ROL (7.40–13.24 mmol O₂ kg^?1 root d.w. h^?1), and porosity (20.91–33.08%) among the cultivars. There were significant negative correlations between As in grains or straw and ROL and porosity, and significant positive correlations between rates of ROL and porosities, respectively. Rice cultivars with high porosities tended to possess higher rates of ROL, and had higher capacities for limiting the transfer of As to aboveground tissues.     

Detection,occurrence and fate of 22 psychiatric pharmaceuticals in psychiatric hospital and municipal wastewater treatment plants in Beijing,China

The liquid chromatography–electrospray ionization-tandem mass spectrometer (LC–MS/MS) method coupled with an automated solid-phase extraction procedure has been developed to identify 22 psychiatric pharmaceuticals, including seven anxiolytic-sedative-hypnotics, six antidepressants, and nine anti-schizophrenia drugs, in wastewater samples from two psychiatric hospital wastewater treatment plants (P-WWTPs) and three municipal wastewater treatment plants (M-WWTPs) in Beijing, China. Analyte recoveries from spiking experiments in the WWTP influent and effluent at three concentrations ranged from 70% to 110%, excluding sulpiride, ziprasidone, and olanzapine. Method detection limits for five, eight, and nine analytes in the WWTP influent and effluent were 20–80, 1–16, and <1 ng L^?1, respectively. High psychiatric pharmaceutical concentrations (e.g., ～942 ng L^?1oxazepam, 5552–12,782 ng L^?1 clozapine, 2762–9832 ng L^?1sulpiride, and 2030–4967 ng L^?1quetiapine) were frequently observed in P-WWTP influent compared to M-WWTPs. Although P-WWTPs typically had higher removal rates, significantly higher concentrations of the target compounds were observed in the P-WWTP secondary effluent than in the M-WWTP influent (e.g., ～752 ng L^?1oxazepam, ～8183 ng L^?1 clozapine, ～10,833 ng L^?1sulpiride, and ～1168 ng L^?1quetiapine). Thus, the discharge control of psychiatric pharmaceuticals from psychiatric hospitals requires improvement.     

Air–water exchange fluxes of polycyclic aromatic hydrocarbons in the tropical coast,Taiwan

Air–water exchange fluxes of polycyclic aromatic hydrocarbons (PAHs) were simultaneously measured in air and water samples from two sites on the Kenting coast, located at the southern tip of Taiwan, from January to December 2010. There was no significant difference in the total PAH (t-PAH) concentrations in both gas and dissolved phases between these two sites due to the less local input which also coincided to the low levels of t-PAH concentration; the gas and dissolved phases averaged 1.29 ± 0.59 ng m^?3 and 2.17 ± 1.19 ng L^?1 respectively. The direction and magnitude of the daily flux of PAHs were significantly influenced by wind speed and dissolved PAH concentrations. Individual PAH flux ranged from 627 ng m^?2 d^?1 volatilization of phenanthrene during the rainy season with storm–water discharges raising dissolved phase concentration, to 67 ng m^?2 d^?1 absorption of fluoranthene during high wind speed periods. Due to PAH annual fluxes through air–water exchange, Kenting seawater is a source of low molecular weight PAHs and a reservoir of high molecular weight PAHs. Estimated annual volatilization fluxes ranged from 7.3 μg m^?2 yr^?1 for pyrene to 50 μg m^?2 yr^?1 for phenanthrene and the absorption fluxes ranged from ?2.6 μg m^?2 yr^?1 for chrysene to ?3.5 μg m^?2 yr^?1 for fluoranthene.