China has been confronted with serious water quality deterioration concurrent with rapid socioeconomic progress during the past 40 years. Consequently, knowledge about economic growth and lake water quality dynamics is important to understand eutrophication processes. Objectives were to (i) reconstruct historical nutrient accumulation and the basin economic progress on burial flux (BF); (ii) determine forms and structures of nitrogen (N) and phosphorus (P) in sediment and water using six cores in three of the most severely eutrophic lake areas in China (i.e., Eastern Plain, Yunnan-Guizhou Plain, and Inner Mongolia–Xinjiang regions). Results suggest that BFs of total nitrogen (TN) continued to increase in sediment, whereas total phosphorus (TP) levels were consistent or only slightly increased, except in highly polluted lakes during the past decades. Similar results were observed for concentrations of nutrients in water (i.e., increased N/P). This historical distribution pattern was correlated to long-term fertilization practices of farmers in the watershed (N fertilization exceeds that of P) and was contingent upon pollution control policies (e.g., emphasized P whereas N was ignored). Vertical profiles of BFs indicated that lake nutrient accumulation included three stages in China. Nutrient accumulation started in the 1980s, accelerated from the 1990s, and then declined after 2000. Before the 1980s, nutrients were relatively low and stable, with nutrient inputs being controlled by natural processes. Thereafter, N- and P-bound sediments dramatically increased due to the increasing influence of anthropogenic processes. Nutrients were primarily derived from industries and domestic sewage. After 2000, BFs of nutrients were steady and even decreased, owing to implementation of watershed load reduction policies. The decreasing NaOH-extracted P (Fe/Al–P) and increasing organic phosphorus (OP) indicated that the source of exogenous pollution underwent a shift. Inputs of nutrients were predominantly from agricultural and domestic sewage, whereas industrial pollution has been gradually controlled in most of the watersheds. Historical nutrient dynamics suggest that the economy of China is growing at the expense of its aquatic ecological environments. Therefore, more attention to nutrient export to groundwater resulting from economic development is important for further aquatic ecosystem deterioration and eutrophication in China.

Studies of metal accumulation in fish are mainly focused on the muscle tissue, while the metal accumulation patterns in other tissues have been largely neglected. Muscle is not always a good indicator of the whole fish body contamination. Elemental accumulation in many fish tissues and organs and their potential use in monitoring programs have not received proper attention. In the present study, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Se, and Zn concentrations were assessed by inductively coupled plasma mass spectrometry (ICP-MS) in the following 14 tissues of the wels catfish (Silurus glanis) from the Danube River: muscle, gills, spleen, liver, kidneys, intestine, gizzard, heart, brain, gallbladder, swim bladder, vertebra, operculum, and gonads. A high level of differential elemental accumulation among the studied tissues was observed. The maximum overall metal accumulation was observed in the vertebra, followed by the kidneys and liver, with the metal pollution index (MPI) values of 0.26, 0.25, and 0.24, respectively. The minimum values were observed in the gallbladder, muscle, brain, and swim bladder, with MPI values of 0.03, 0.06, 0.07, and 0.09, respectively. Average metal concentrations in the fish muscle were below the maximum allowed concentrations for human consumption. The mean As, Cd, Pb, Cu, Fe, and Zn concentrations in the muscle were 0.028, 0.001, 0.001, 0.192, 3.966, and 3.969 μg/g wet weight, respectively. We believe that the presented findings could be of interest for the scientific community and freshwater ecosystem managers. There is a need for further research that would assess less studied tissues in different fish species.

Crop irrigation with heavy metal-contaminated effluents is increasingly common worldwide and necessitates management strategies for safe crop production on contaminated soils. This field study examined the phytoavailability of three metals (Cd, Cu, and Zn) in two cereal (wheat, maize) and legume (chickpea, mungbean) crops in response to the application of either phosphatic fertilizer or sewage-derived water irrigation over two successive years. Five fertilizer treatments, i.e. control, recommended nitrogen (N) applied alone and in combination of three levels of phosphorus (P), half, full and 1.5 times of recommended P designated as N₀P₀, N₁P₀, N₁P₀.₅, N₁P₁.₀, and N₁P₁.₅, respectively. Tissue concentrations of Cd, Cu, Zn, and P were determined in various plant parts, i.e., root, straw, and grains. On the calcareous soils studied while maximum biomass production was obtained with application of P at half the recommended dose, the concentrations of metals in the crops generally decreased with increasing P levels. Tissue metal concentrations increased with the application of N alone. Translocation and accumulation of Zn and Cu were consistently higher than Cd. And the pattern of Cd accumulation differed among plant species; more Cd being accumulated by dicots than monocots, especially in their grains. The order of Cd accumulation in grains was maize > chickpea > mungbean > wheat. Mungbean and chickpea straws also had higher tissue Cd concentration above permissible limits. The two legume species behaved similarly, while cereal species differed from each other in their Cd accumulation. Metal ion concentrations were markedly higher in roots followed by straw and grains. Increasing soil-applied P also increased the extractable metal and P concentrations in the post-harvest soil. Despite a considerable addition of metals by P fertilizer, all levels of applied P effectively decreased metal phytoavailability in sewage-irrigated soils, and applying half of the recommended dose of P fertilizer was the most feasible solution for curtailing plant metal uptake from soils. These findings may have wide applications for safer crop production of monocot species when irrigating crops with sewage effluent-derived waters.

The bioaccumulation efficiency of cadmium (Cd) by fenugreek (Trigonella foenum-graecum) was examined using different concentrations of CdCl₂. The germination rate was similar to control except at 10 mM Cd. However, early seedling growth was quite sensitive to the metal from the lowest Cd level. Accordingly, amylase activity was reduced substantially on treatment of seeds with 0.5, 1, and 10 mM Cd. Cadmium also affected various other plant growth parameters. Its accumulation was markedly lower in shoots as compared to roots, reducing root biomass by almost 50 %. Plants treated with 1 and 5 mM Cd presented chlorosis due to a significant reduction in chlorophyll b especially. Furthermore, at Cd concentrations greater than 0.1 mM, plants showed several signs of oxidative stress; an enhancement in root hydrogen peroxide (H₂O₂) level and in shoot malondialdehyde (MDA) content was observed. Conversely, antioxidant enzyme activities (superoxide dismutase (SOD), ascorbate peroxidase (APX), and catalase (CAT)) increased in various plant parts. Likewise, total phenolic and flavonoid contents reached their highest values in the 0.5 mM Cd treatment, consistent with their roles in quenching low concentrations of reactive oxygen species (ROS). Consequently, maintaining oxidant and antioxidant balance may permit fenugreek to hyperaccumulate Cd and allow it to be employed in extremely Cd polluted soils for detoxification purposes.

Although used motor oil from automobiles is one of the major pollutants through storm water in urban environments leading to contamination of water bodies, very little information is available on its toxicity towards growth of microalgae. Also, to our knowledge, there are no data on the used motor oil-induced oxidative stress in microalgae. We therefore investigated the toxicity of used and fresh motor oil on growth and antioxidant enzymes of a microalga, Pseudokirchneriella subcapitata. In general, used oil was more toxic to the alga than fresh oil. Used oil at 0.20 % inhibited algal growth, measured in terms of chlorophyll a, by 44 % while fresh oil was nontoxic up to 2.8 %. Water-accommodated fraction (WAF) of the used oil at >50 % concentration exhibited significant toxicity while WAF from fresh oil was nontoxic even up to 100 %. Used oil and its WAF, even at lower concentrations, increased the levels of antioxidant enzymes indicating algal response to the toxicity stress. When the alga was exposed to WAF from fresh motor oil, no alterations in the antioxidant enzyme levels were evident. The present investigation suggests that contamination of aquatic systems with used oil could potentially affect the ecosystem health via disruption of primary producers that are located at the base of the food chain.

Three types of chitosan with high (3.40 × 10⁶), medium (2.11 × 10⁵), and low (5.89 × 10⁴) molecular weights were chosen as ligands to synthesize chitosan magnesium, calcium, iron(III), and zinc coordination complexes. Degradation of four organophosphorous pesticides (dichlorvos, omethoate, dimethoate, and chlorpyrifos) by the above complexes in a heterogeneous system was studied using solid-phase extraction (SPE) and gas chromatography (GC). The degradation effect is related to the different types of chitosan, metal, and organophosphorus pesticides (OPs). Complexes of transition metals and the low molecular weight chitosan showed high hydrolytic activity. The chitosan-iron(III) complex was further used to study its catalytic kinetics on the hydrolysis of OPs. At pH 7.0 and 20 °C, the half-life of dichlorvos hydrolyzed by chitosan iron(III) was 52 h, whereas that of spontaneous dichlorvos hydrolysis was 105 h. The degradation ratio of omethoate and dimethoate increased to 38 and 52 %, respectively, which were 34 and 48 % higher than the control after 6 days at pH 7.0 and 20 °C. For all tested conditions, an increase of pH and temperature resulted in a higher degradation rate.

The degradation of bisphenol A (BPA) by Chlorella sorokiniana and BPA-degrading bacteria was investigated. The results show that BPA was partially removed by a monoculture of C. sorokiniana, but the remaining BPA accounted for 50.2, 56.1, and 60.5 % of the initial BPA concentrations of 10, 20, and 50 mg L⁻¹, respectively. The total algal BPA adsorption and accumulation were less than 1 %. C. sorokiniana-bacterial system effectively removed BPA with photosynthetic oxygen provided by the algae irrespective of the initial BPA concentration. The growth of C. sorokiniana in the algal system was inhibited by BPA concentrations of 20 and 50 mg L⁻¹, but not in the algal-bacterial system. This observation indicates that bacterial growth in the algal-bacterial system reduced the BPA-inhibiting effect on algae. A total of ten BPA biodegradation intermediates were identified by GC-MS. The concentrations of the biodegradation intermediates decreased to a low level at the end of the experiment. The hypothetical carbon mass balance analysis showed that the amounts of oxygen demanded by the bacteria are insufficient for effective BPA degradation. However, adding an external carbon source could compensate for the oxygen shortage. This study demonstrates that the algal-bacterial system has the potential to remove BPA and its biodegradation intermediates.

We present a sensitivity analysis of a reactive transport model of mercury (Hg) fate in contaminated soil systems. The one-dimensional model, presented in Leterme et al. (2014), couples water flow in variably saturated conditions with Hg physico-chemical reactions. The sensitivity of Hg leaching and volatilisation to parameter uncertainty is examined using the elementary effect method. A test case is built using a hypothetical 1-m depth sandy soil and a 50-year time series of daily precipitation and evapotranspiration. Hg anthropogenic contamination is simulated in the topsoil by separately considering three different sources: cinnabar, non-aqueous phase liquid and aqueous mercuric chloride. The model sensitivity to a set of 13 input parameters is assessed, using three different model outputs (volatilized Hg, leached Hg, Hg still present in the contaminated soil horizon). Results show that dissolved organic matter (DOM) concentration in soil solution and the binding constant to DOM thiol groups are critical parameters, as well as parameters related to Hg sorption to humic and fulvic acids in solid organic matter. Initial Hg concentration is also identified as a sensitive parameter. The sensitivity analysis also brings out non-monotonic model behaviour for certain parameters.

Combination of ozone together with electrolysis (ozone-electrolysis) is a promising wastewater treatment technology. This work investigated the potential use of carbon nanotube (CNT)-based gas diffusion cathode (GDC) for ozone-electrolysis process employing hydroxyl radicals (·OH) production as an indicator. Compared with conventional active carbon (AC)-polytetrafluoroethylene (PTFE) and carbon black (CB)-PTFE cathodes, the production of ·OH in the coupled process was improved using CNTs-PTFE GDC. Appropriate addition of acetylene black (AB) and pore-forming agent Na₂SO₄ could enhance the efficiency of CNTs-PTFE GDC. The optimum GDC composition was obtained by response surface methodology (RSM) analysis and was determined as CNTs 31.2 wt%, PTFE 60.6 wt%, AB 3.5 wt%, and Na₂SO₄ 4.7 wt%. Moreover, the optimized CNT-based GDC exhibited much more effective than traditional Ti and graphite cathodes in Acid Orange 7 (AO7) mineralization and possessed the desirable stability without performance decay after ten times reaction. The comparison tests revealed that peroxone reaction was the main pathway of ·OH production in the present system, and cathodic reduction of ozone could significantly promote ·OH generation. These results suggested that application of CNT-based GDC offers considerable advantages in ozone-electrolysis of organic wastewater.

Throughout history, synanthropic Musca domestica had remained a worldwide problem whenever poor sanitation and bad hygienic conditions exists. Houseflies growing resistance to chemical insecticides are a rising environmental problem that necessitates search for alternatives. Mentha cervina, Ocimum basilicum, and Coriandrum sativum were tested for bioactivity on M. domestica adults and larvae. They are culinary Mediterranean plants. In adulticidal bioassay, using both CDC bottles and fumigation techniques, basil was the most effective extract with LC₅₀ 1.074 and 34.996 g/L, respectively. Concerning larvicidal bioassay by fumigation technique, coriander had the highest toxicity index with LC₅₀ 29.521 g/L. In both dipping and feeding technique, basil had the highest toxicity with LC₅₀ 32.643 and 0.749 g/L, respectively. Basil showed the highest toxicity results in four out of the five models tested followed by coriander then mint; this result highlights the potentiality of basil as a green insecticide in management of flies and opens new insight in the industrialization of basil-based fly control products.