Morphological plasticity of submerged macrophyte Potamogeton wrightii Morong under different photoperiods and nutrient conditions

The morphological plasticity of the submerged macrophyte Potamogeton wrightii under different nutrient conditions and photoperiods was measured in a laboratory controlled experiment for 70 days in Japan. Six treatments were used in this experiment (3 × 2 factorial design with three replications) which consisted of three photoperiods and two nutrient conditions. Both photoperiod and nutrient condition had a pronounced effect on shoot and leaf morphology in P. wrightii. New shoot recruitment, and the length of main and new shoots gradually decreased with shortening photoperiod under both nutrient treatments. Plants under an 8 h photoperiod and high nutrient levels generated significantly more dead leaves (7.42 leaf·shoot^?1) and decomposed shoots (1.3 shoots·pot^?1) than plants under other treatments. Under short photoperiods (12 and 8 h) plants failed to produce flowering spikes in both nutrient conditions. In high nutrient conditions, P. wrightii produced shorter shoots, fewer leaves with shorter and narrower laminas, and smaller petioles compared with plants in the low nutrient condition. This may be adaptive under high nutrient conditions because it lowers foliar uptake and, thus, nutrient toxicity.     

Rice seedlings under cadmium stress: effect of silicon on growth,cadmium uptake,oxidative stress,antioxidant capacity and root and leaf structures

In this study, the effect of silicon (Si) addition on cadmium (Cd) toxicity in rice seedlings was investigated. After a series of screening experiments, 50 μmol·L^?1 of Cd and 10 μ mol·L^?1 of Si were selected. Treatment of rice seedlings with Cd (50 μ mol·L^?1) resulted in significant accumulation of this metal in roots and shoots. The data revealed that accumulation of Cd resulted in oxidative stress in rice seedlings as evidenced by increased accumulation of hydrogen peroxide (H₂O₂) and malondialdehyde (MDA; a peroxidation product of lipids). However, addition of Si (10 μ mol·L^?1) together with Cd prevented accumulation of Cd, H₂O₂ and MDA. Antioxidant capacity was decreased by Cd but enhanced by Si addition. Cd decreased the length and frequency of root hairs, stomatal frequency, and distorted leaf mesophyll cells and vascular bundles. However, addition of Si together with Cd reduced these abnormalities. The results showed that addition of exogenous Si protected rice seedlings against Cd toxicity by preventing Cd accumulation and oxidative stress (H₂O₂ and MDA accumulation) by increasing Si accumulation and antioxidant capacity, which maintained the structure and integrity of leaf and root.     

Characterisation and classification of hoarfrost samples collected in Poland (2003–2005) by discriminant analysis

Discharges of nutrients, urea, dissolved organic matter and heavy metals by a sewage underwater pipeline are analysed in comparison to environmental conditions in a shallow coastal zone. Variable thermo-haline stratifications of the water column and currents in upper (2.62–34.97 cm s^?1) and deeper (0.83–10.91 cm s^?1) layers drive vertical diffusion and lateral transport of wastewaters. Loads of reactive phosphorus (0.13 tons d^?1) and ammonium (1.62 tons d^?1) by the pipeline are not negligible compared to the major river loads in the gulf. High concentrations of urea (≤11.51 μmol N dm^?3) were found in the area of wastewater release. Ammonium uptake (6.14–534 nmol N dm^?3 h^?1) strongly exceeded nitrate uptake (0.19–138 nmol N dm^?3 h^?1), indicating that discharges of ammonium by the pipeline are actively assimilated by plankton community even at low levels of light. Distribution of Zn (≤27.7 ppb), Cu (≤25.6 ppb), Cd (≤0.80 ppb) and Pb (≤13.5 ppb) in the water column and the measurement of their complex-forming capacity in seawater did not indicate a persistent perturbation of the pelagic environment due to heavy metals.     

The removal of arsenic from water with natural and modified clinoptilolite

The presence of increased arsenic concentrations in Eastern Croatia is a consequence of the geological composition of the soil. Because of its known harmful effects, arsenic removal is of high importance and adsorption represents an attractive and economically efficient approach to arsenic removal. The use of zeolites obtained from the Donje Jesenje deposit, Croatia (CZ) and the Zlatokop deposit in Vranjska Banja, Serbia (SZ) in Na- and Fe–Na-modified forms was investigated in order to effectively remove arsenate and arsenite from aqueous solutions. The adsorption kinetics of arsenic was studied as a function of the initial arsenate and arsenite concentrations (30–300 μg · L^?1), equilibration time (3–48 h), pH (5–10) and in the presence of sulfate and phosphate at initial concentrations of 0.2–0.5 mg · L^?1. In order to estimate sorption constants designating the sorption capacity and affinity of the zeolites samples, the experimental results were fitted to the Langmuir and Freundlich sorption isotherms. Desorption tests conducted with 1–3 mol · L^?1 HCl indicated that arsenate sorption was irreversible. The results obtained indicated that use of the Serbian zeolite in the Fe–Na-modified form (Fe–Na-SZ) was favourable for arsenate removal from water containing up to 30 μg As · L^?1.     

Solar-induced generation of singlet oxygen and hydroxyl radical in sewage wastewaters

Singlet oxygen (¹O₂) and hydroxyl radical (·OH) play an important role in the degradation of pollutants in surface waters. However, the mechanism underlying the photochemical generation of ¹O₂ and ·OH in wastewaters is poorly known. Here we studied the photo-induced generation of ¹O₂ and ·OH in different sewage treatment plant units. The correlation between the generation of ¹O₂ and ·OH and the water constituents was discussed. Our results show that in sewage units the ¹O₂ formation rate ranges from 2.19 × 10^?8 to 6.74 × 10^?8 mol L^?1 s^?1, and the ·OH formation rate ranges from 1.7 × 10^?11 to 3.06 × 10^?10 mol L^?1 s^?1. The average ¹O₂ formation rates in the various sewage units are similar to those in wetland and estuarine waters containing rich dissolved organic matter and 2–4 times higher than those in lake and seawater samples. The average ·OH formation rates of the sewage units are 5–50 times higher than for other water samples reported. The ·OH generation rate increased with the iron content with a correlation coefficient of 0.85, which indicates that the photo-Fenton reaction plays a dominant role in ·OH generation in sewage wastewater.     

Metabolic responses of Azolla pinnata to cadmium stress: photosynthesis,antioxidative system and phytoremediation

This present study deals with the growth, photosynthesis, oxidative stress and phytoremediation character of Azolla pinnata L. exposed to different levels (0.05, 0.1, 0.5, 1.0, 1.5 and 2.0 mg·L^?1) of cadmium (Cd). Significant accumulation of Cd in Azolla fronds was noticed after 24 and 96 h of exposure and the accumulation rate was dose and time dependent. Growth of A. pinnata increased significantly after both exposure times with and without metal. At lower Cd doses (0.05 and 0.1 mg·L^?1), growth and photosynthesis of A. pinnata showed a marginal increase over the respective control, however, at higher Cd doses (0.5, 1.0, 1.5 and 2.0 mg·L^?1), a decreasing trend was noticed. At lower doses, Azolla fronds could counterbalance the negative effect of enhanced levels of superoxide radicals (SOR) and hydrogen peroxide (H₂O₂) through the greater activity of antioxidative enzymes. The decaresing trends in catalase and peroxidase activity at higher Cd doses suggest that Azolla fronds were not able to mitigate the negative effects of H₂O₂, hence an increase in malondialdehyde content was noticed. The study concludes that up to 0.1 ,mg·L^?1 Cd, A. pinnata can flourish and be used as biofertiliser and for phytoremedial purposes in Cd-contaminated fields; beyond this concentration poor growth may restrict its application.     

Heavy metals in the polychaete Glycera longipinnis from the southwest of India

Metal concentrations in sediment and in whole tissue of the benthic polychaete Glycera longipinnis collected along the southwest coast of India were analysed. Relative seasonal accumulation of metals (Cu, Pb, Cr, Ni, Zn, Cd, Hg) was studied by categorising the habitat as less polluted or highly polluted based on metal contamination routed through industrial and urban sources. The metal content in tissues varied seasonally in the ranges, Cu: 2.21–27.08 μg·g^?1, Pb: 0.06–4.92 μg·g^?1, Cr: 1.73–29.20 μg·g^?1, Ni: 1.60–4.61 μg·g^?1, Zn: 14.72–82.30 μg·g^?1, Cd: 0.04–1.38 μg·g^?1and Hg: below decetable limits to 0.86 μg·g^?1. Concentration of heavy metals was found to be high in the whole body of G. longipinnis pooled from the polluted transects. The results of this study suggest that G. longipinnis may act as a useful biological indicator for heavy metal pollution along the southwest coast of India.     

Mercury pollution in the Sonbhadra district of Uttar Pradesh,India, and its health impacts

The Sonbhadra district in the Singrauli area of Uttar Pradesh, India, has many coal mines and thermal power plants and is a critically polluted area. Many residents of this area reported adverse health conditions which may be linked to metal pollution, especially of mercury investigated here.

In May 2012, samples of water (23), soil (7), blood, hair, and nails from persons showing adverse health conditions selected at random were collected and analyzed for total mercury by atomic absorption spectrometry.

Twenty percent drinking water samples contained mercury from 3 to 26 μg L^?1 (3–26 times the permissible limit). Soil samples had 0.5–10.1 mg kg^?1 Hg.

The average concentrations of mercury in human blood, hair, and nails were found to be 34 μg L^?1, 7.4 mg kg^?1, and 0.8 mg kg^?1, respectively. Mercury concentrations in the blood of these persons were 45 and 28 μg L^?1 on average in the case of men and women. This is much higher than the safe level of 5.8 μg L^?1 set by the United States Environmental Protection Agency (USEPA).

It was concluded that all residents of Sonbhadra sampled could be suffering from mercury toxicity as the area is polluted by Hg released from the coal-fired thermal power plants.     

Antiaggregant and toxic properties of different solutions on hemocytes of three freshwater bivalves

Hemocytes are main blood components of bivalves playing important roles in toxicological and immune responses. Consequently, a study on these cells may be useful to understand the invertebrate immunological systems. The aim of the present study was to find the best antiaggregant solution, based on its capacity of preserving the natural morphology and viability of hemocytes from the freshwater bivalves, Anodonta cygnea, Unio delphinus, and Corbicula fluminea. Hemocytes from the three species were collected and maintained in different antiaggregant solutions, i.e., ethylenediaminetetraacetic acid (EDTA), EDTA-citrate, modified Alsever solution (MAS), N-ethylmaleimide (NEM), NEM-NaCl, and heparin. The cell morphology and viability were analyzed periodically with light microscopy techniques. Between these assays with various antiaggregant solutions, the best results were obtained with NEM at a concentration of 0.05 mol·L^?1. It is also shown that, as expected, the osmolarity of the antiaggregant solutions plays a very important role in cell viability. Based on this study, NEM at 0.05 mol·L^?1 was considered an adequate antiaggregant solution for future research on immunological and toxicological responses and other physiological studies of freshwater bivalve hemocytes.     

Denitrification in bottom sediment near oil production facilities off the Louisiana Gulf Coast

There is little information on denitrification in Gulf of Mexico bottom sediment. Potential denitrification rates in surface sediment were measured along transects legs extending 0–800 m from two offshore oil production platforms. The average potential denitrification ranged from approximately 50 mg N m^?2 d^?1 in surface sediment near the platforms to 15 mg N m^?2 d^?1 in sediment 800 m from the platforms. Measured denitrification rates were correlated to a higher organic matter content in sediment nearer the platforms. This research examined only a small component of nitrogen processing in Gulf of Mexico sediment. Additional research should examine the effect of nitrogen loading and temporal and spatial variability on denitrification rate.     

Ultrastructural responses and oxidative stress induced by cypermethrin in the liver of Labeo rohita

The present study was conducted to establish the relationship between selected oxidative stress parameters and ultrastructural responses in liver tissue of Labeo rohita fingerlings exposed to cypermethrin. Fish were exposed to lethal (4.0 μg L^?1) and sublethal (0.4 μg L^?1) concentrations of cypermethrin for a period of 24, 48, 72 and 96 h for acute studies and 1, 5, 10 and 15 days for subacute studies, respectively. Results showed increased catalase (CAT) and protease activity, hydrogen peroxide (H₂O₂), malondialdehyde (MDA), protein carbonyls and free amino acid (FAA) levels at both concentrations. This suggests participation of free-radical-induced oxidative cell injury in mediating the hepatotoxicity of cypermethrin. In corroboration of this, ultrastructural lesions witnessed a reduction in the number of cell organelles, swollen, vacuolated and condensed mitochondria, dilated rough endoplasmic reticulum, and reduced numbers of smooth enodplasmic reticulum, peroxisomes and lysosomes at the lethal (4.0 μg L^?1) concentration. At the sublethal (0.4 μg L^?1) concentration, cytoplasmic vacuolation, condensed, vacuolated and swollen mitochondria, dilated rough endoplasmic reticulum and an absence of hepatocyte microvilli were prominent. Ultrastructural changes were exhibited as subcellular responses due to the imbalance in cellular oxidative status by means of oxidative damage.     

Combination system of full-scale constructed wetlands and wetland paddy fields to remove nitrogen and phosphorus from rural unregulated non-point sources

Constructed wetlands (CWs) have been used effectively to remove nitrogen (N) and phosphorus (P) from non-point sources. Effluents of some CWs were, however, still with high N and P concentrations and remained to be pollution sources. Widely distributed paddy fields can be exploited to alleviate this concern. We were the first to investigate a combination system of three-level CWs with wetland paddy fields in a full scale to remove N and P from rural unregulated non-point sources. The removal efficiencies (REs) of CWs reached 57.3 % (37.4–75.1 %) for N and 76.3 % (62.0–98.4 %) for P. The CWs retained about 1,278 kg N ha^?1 year^?1 and 121 kg P ha^?1 year^?1. There was a notable seasonal change in REs of N and P, and the REs were different in different processing components of CWs. The removal rates of wetland paddy fields adopt “zero-drainage” water management according to local rainfall forecast and physiological water demand of crop growth reached 93.2 kg N ha^?1 year^?1 and 5.4 kg P ha^?1 year^?1. The rice season had higher potential in removing N and P than that in the wheat season. The whole combined system (0.56 ha CWs and 5.5 ha wetland paddy fields) removed 1,790 kg N year^?1 and 151 kg P year^?1, which were higher than those from CWs functioned alone. However, another 4.7-ha paddy fields were needed to fully remove the N and P in the effluents of CWs. The combination of CWs and paddy fields proved to be a more efficient nutrient removal system.     

Decolorization of azo dyes by a salt-tolerant Staphylococcus cohnii strain isolated from textile wastewater

The salt-tolerant Staphylococcus cohnii strain, isolated from textile wastewater, has been found effective on decolorizing several kinds of azo dyes with different structures. The optimal conditions for azo dye acid red B (ARB) decolorization by S. cohnii were determined to be pH = 7.0 and 30°C. The decolorization efficiency increased with the increase of the salinity concentration, and around 90% of ARB (100 mg·L^?1) could be decolorized in 24 h when the salinity concentration was up to 50 g·L^?1. Moreover, the strain could still decolorize 19% of ARB in 24 h even when the NaCl concentration was increased to 150 g·L^?1. Meanwhile, the dependence of the specific decolorization rate by S. cohnii on the ARB concentration could be described with Michaelis-Menten kinetics (K _m = 585.7mg·L^?1, V _max = 109.8 mg·g cell^?1·h^?1). The addition of quinone redox mediator, named 2-hydroxy-1,4-naphthoquinone and anthraquinone-2,6-disulfonate, significantly accelerated the decolorization performance of S. cohnii. Furtherly, the activities of azoreductase (0.55 ??mol·mg protein^?1·min^?1) and Nicotineamide adenine dinucleotide-dichlorophenol indophenol (NADH-DCIP) reductase (8.9 ??mol·mg protein^?1·min^?1) have been observed in the crude cell extracts of S. cohnii. The decolorization products of ARB were analyzed by HPLC-MS, and the results indicated the reductive pathway was responsible for azo dye decolorization by S. cohnii.     

Ligand-less in situ surfactant-based solid phase extraction for preconcentration of silver from natural water samples prior to its determination by atomic absorption spectroscopy

A simple and rapid ligand-less in situ surfactant-based solid phase extraction method for preconcentration of silver from water samples is developed. In this method, a cationic surfactant containing a proper alkyl group (n-dodecyltrimethylammonium bromide) is dissolved in the aqueous sample and then a proper ion-pairing agent (ClO₄^?) is added. Due to the interaction between surfactant and ion-pairing agent, solid particles are formed and used for adsorption of silver carbonate. After centrifugation, the sediment is dissolved in 2.0 mL 1 M HNO₃ in ethanol and then aspirated directly into the flame atomic absorption spectrometer. Variables affecting the extraction efficiencies such as pH, concentrations of surfactant and CO₃^2?, ion pair concentration, and extraction time, are optimized. Under such conditions, the calibration curve is linear from 3 to 700 μg L^?1. Detection limit is 1.1 μg L^?1 with an enrichment factor of 37. The relative standard deviation for eight replicate measurements of 100 μg L^?1 is 2.1%. The method has been applied for the determination of silver in water samples.     

Decomposition of perfluorooctanoic acid by microwaveactivated persulfate: Effects of temperature, pH, and chloride ions

Microwave-hydrothermal treatment of persistent and bioaccumulative perfluorooctanoic acid (PFOA) in water with persulfate (S₂O ₈ ^2? ) has been found effective. However, applications of this process to effectively remediate PFOA pollution require a better understanding on free-radical scavenging reactions that also take place. The objectives of this study were to investigate the effects of pH (pH = 2.5, 6.6, 8.8, and 10.5), chloride concentrations (0.01?C0.15 mol·L^?1), and temperature (60°C, 90°C, and 130°C) on persulfate oxidation of PFOA under microwave irradiation. Maximum PFOA degradation occurred at pH 2.5, while little or no degradation at pH 10.5. Lowering system pH resulted in an increase in PFOA degradation rate. Both high pH and chloride concentrations would result in more scavenging of sulfate free radicals and slow down PFOA degradation. When chloride concentrations were less than 0.04 mol·L^?1 at 90°C and 0.06 mol·L^?1 at 60°C, presence of chloride ions had insignificant impacts on PFOA degradation. However, beyond these concentration levels, PFOA degradation rates reduced significantly with an increase in chloride concentrations, especially under the higher temperature.     

Effects of ethyl 2-methyl acetoacetate (EMA) on the growth of Phaeodactylum tricornutum and Skeletonema costatum

We investigated the effects of ethyl 2-methyl acetoacetate (EMA) on growth of the marine diatom algae Phaeodactylum tricornutum (P. tricornutum) and Skeletonema costatum (S. costatum). Growth of P. tricornutum was significantly inhibited by the minimum concentration (3.5 mmol·L ^?1) of EMA at lower initial algal densities (IADs) (3.6×10⁴ and 3.3×10⁵ cells·mL ^?1). However, at the highest IAD, significant growth inhibition was found at above 7 mmol·L ^?1 of EMA exposure. In S. costatum, EMA concentrations of 10.5 mmol·L ^?1 or more significantly inhibited growth at lower IAD (3×10⁴ and 1.8×10⁵ cells·mL ^?1); at the highest IAD, only EMA concentrations above 14 mmol·L ^?1 obviously inhibited the growth of S. costatum. Changes in specific growth rates and pigment were consistent with algal growth, but only at higher EMA concentrations or lower IAD values was the ratio of chlorophyll a (Chla) to carotenoid significantly lower than the control. Medium effective concentration (EC ₅₀) values were in the order 4.07, 8.03 and 12.27 mmol·L ^?1 for P. tricornutum and 7.48, 11.92 and 17.22 mmol·L ^?1 for S. costatum. All these results show that the effect of EMA on the growth of algae was species specific and mainly depended on IAD, which might be an important factor to influence algal growth.     

Diffusive boundary layers and photosynthesis of the epilithic algal community of coral reefs

The effects of mass transfer resistance due to the presence of a diffusive boundary layer on the photosynthesis of the epilithic algal community (EAC) of a coral reef were studied. Photosynthesis and respiration of the EAC of dead coral surfaces were investigated for samples from two locations: the Gulf of Aqaba, Eilat (Israel), and One Tree Reef on the Great Barrier Reef (Australia). Microsensors were used to measure O₂ and pH at the EAC surface and above. Oxygen profiles in the light and dark indicated a diffusive boundary layer (DBL) thickness of 180–590 μm under moderate flow (~0.08 m s^?1) and >2,000 μm under quasi-stagnant conditions. Under light saturation the oxygen concentration at the EAC surface rose within a few minutes to 200–550% air saturation levels under moderate flow and to 600–700% under quasi-stagnant conditions. High maximal rates of net photosynthesis of 8–25 mmol O₂ m^?2 h^?1 were calculated from measured O₂ concentration gradients, and dark respiration was 1.3–3.3 mmol O₂ m^?2 h^?1. From light–dark shifts, the maximal rates of gross photosynthesis at the EAC surface were calculated to be 16.5 nmol O₂ cm^?3 s^?1. Irradiance at the onset of saturation of photosynthesis, E _k, was <100 µmol photons m^?2 s^?1, indicating that the EAC is a shade-adapted community. The pH increased from 8.2 in the bulk seawater to 8.9 at the EAC surface, suggesting that very little carbon in the form of CO₂ occurs at the EAC surface. Thus the major source of dissolved inorganic carbon (DIC) must be in the form of HCO₃ ^?. Estimates of DIC fluxes across the DBL indicate that, throughout most of the daytime under in situ conditions, DIC is likely to be a major limiting factor for photosynthesis and therefore also for primary production and growth of the EAC.     

Ultrasound-assisted emulsification/microextraction based on solidification of trace amounts of thallium prior to graphite furnace atomic absorption spectrometry determination

In the present work, determination of ultratrace amounts of thallium in water samples was performed by ultrasound-assisted emulsification microextraction based on solidification of a floating organic drop as sample preparation method prior to furnace atomic absorption spectrometry. 1-(2-Pyridylazo)-2-naphthol was used as chelating agent. The factors influencing the complex formation and extraction, such as pH of the aqueous solution, the type and the volume of extraction solvent, the volume of chelating agent solution, and the extraction time were investigated. Under optimized conditions, the enrichment factor was 200. The calibration graph was linear from 0.2 to 10.0 μg L^?1 with a correlation coefficient of 0.9966, the detection limit was 0.03 μg L^?1 and reproducibility was ±3.3% (C = 5.0 μg L^?1, n = 8). The method was successfully applied for the determination of thallium in water samples.     

Evaluation of the toxicity of tetrabromobisphenol A and some of its oxidation products using a micro-scale algal growth inhibition test

A micro-scale algal growth inhibition (μ-AGI) test using a common micro-plate based fluorometric detection was used to demonstrate the effects of humic substances (HSs) on the toxicity of tetrabromobisphenol A (TBBPA) and its oxidative decomposition products 2,5-dibromo-1,4-benzoquinone (2,5-DBBQ), 2,5-dibromohydroquinone (2,5-DBHQ), 2,6-dibromobenzoquinone (2,6-DBBQ), and 2,6-dibromophenol (2,6-DBP) to Pseudokirchneriella subcapitata. The EC₅₀ values were: EC_50(TBBPA) = 7 mg L^?1, EC_50(2,5-DBHQ) = 7 mg L^?1, EC_50(2,5-DBBQ) = 19 mg L^?1, EC_50(2,6-DBP) = 49 mg L^?1, and EC_50(2,6-DBBQ) = 13 mg L^?1. The toxicity of the chemicals was slightly lower in the presence of HA. The toxicity of TBBPA decomposed by a biomimetic catalytic system consisting of iron (III) 5,10,15,20-tetrakis (p-sulfonatophenyl) porphyrin (Fe(III)-TPPS) and KHSO₅ was also evaluated using P. subcapitata and Chlamydomonas reinhardtii.