全球价值链视角下中国农产品贸易隐含氮、磷、钾研究

基于GTAP数据库提供的多区域投入产出表,采用全球价值链方法测算中国农产品贸易中隐含的化肥转移,并按照农产品最终消费的地理位置将其分解为四部分。研究发现：（1）中国农产品进口为国内节约640万t化肥（占我国化肥用量的13%）,同时引起全球化肥用量节约285万t,为缓解全球资源和环境压力做出贡献;（2）中国农产品贸易深度参与全球价值链,进口农产品中隐含的化肥有12%会再次出口到全球,意味着农产品贸易背后隐含的资源到达中国后会再次出口,形成多次跨境转移。建议在全球价值链视角下更为客观地估算农产品贸易隐含的化肥及其他资源环境问题,倡导共同承担贸易引致的资源环境问题。     

Groundwater quality of north-east Libya

The quality of groundwater was assessed to their suitability for drinking at six places of north-east Libya viz. El-Marj, Albayda, Shahat, Susa, Ras al-Hilal and Derna, during November, 2003 to March, 2004, by determining their physicochemical parameters (17 parameters) and water quality index (15 parameters). The temperatures of water samples averaged 15.1 degree C, pH values were alkaline and dissolved oxygen values were in safe ranges. Electrical conductivity, total dissolved solids and hardness of water at all places except Susa were within the standard limits. Alkalinity of well water at all six places exceeded, and chlorine and chloride (except Susa) were within the desirable limits set for them. Fluoride and nitrate contaminations of well water were not observed, and only very low values of phosphorus, manganese, chromium, iron and zinc were recorded. Copper in well water was generally high, and at Susa and Ras al-Hilal, it exceeded the desirable limit. Parametric ratios showed that all parameters studied except those of pH, dissolved oxygen, alkalinity and total chlorine originated from sources different from that of hardness. Water quality index (WQI) revealed that well water of Albayda and Shahat were good for drinking and were only slightly polluted, whereas those of El-Marj, Ras al-Hilal and Derna were moderately polluted. However, the well water of Susa was excessively polluted and was unsuitable for drinking. Suitable suggestions were made to improve the quality of groundwater of N.E. Libya.     

Selective removal of some polyhydric phenols from aqueous solution by ferric antimonate

Ferric antimonate, a cation-exchanger, has been investigated as an adsorbent for the removal of phenol and polyhydric phenols from aqueous solution. It has been found that ferric antimonate in H+ form selectively adsorbs polyhydric phenols having hydroxyl groups on adjacent positions. While phenol, resorcinol, and quinol did not show any appreciable adsorption, catechol, pyrogallol, and gallic acid having hydroxyl groups on adjacent positions exhibited considerable adsorption on ferric antimonate. Batch equilibrium experiments were carried out to study the effect of contact time, initial concentration of phenolic compounds, and temperature on the adsorption of phenolic compounds on ferric antimonate. The equilibrium time was found to be 1.5 hours for gallic acid and pyrogallol and 2 hours for catechol and salicylic acid. The adsorption data of the phenols at temperatures of 30 degrees, 40 degrees, and 50 degrees C have been described by Langmuir and Freundlich isotherm models. The best fit was obtained with the Langmuir model in the whole range of concentrations studied at all temperatures, indicating a monolayer adsorption onto a homogeneous adsorption surface. On the basis of the Langmuir isotherm, the maximum adsorption capacity of ferric antimonate for gallic acid, pyrogallol, catechol, and salicylic acid was found to be 3.915, 3.734, 2.397, and 2.758 mg/g, respectively at 30 degrees C. The maximum sorption capacity of ferric antimonate for the phenolic compounds studied is in the following order: gallic acid > pyrogallol > salicylic acid > catechol. The adsorption of phenolic compounds was found to decrease with an increase in temperature. Thermodynamic parameters like free energy, enthalpy, and entropy changes were calculated and discussed. The adsorption of polyhydric phenols on ferric antimonate is exothermic and spontaneous in nature.     

Contamination levels of selected organochlorine and organophosphate pesticides in the Selangor River, Malaysia between 2002 and 2003

In Malaysia, rivers are the main source of public water supplies. This study was conducted from 2002 to 2003 to determine the levels of selected organochlorine and organophosphate pesticides in the Selangor River in Malaysia. Surface water samples have been collected seasonally from nine sites along the river. A liquid-liquid extraction followed by gas chromatography-mass spectrometry technique was used to determine the trace levels of these pesticide residues. The organochlorine pesticides detected were lindane, heptachlor, endosulfan, dieldrin, endosulfan sulfate, o,p'-DDT, p,p'-DDT, o,p'-DDE and p,p'-DDE whereas for organophosphate pesticides, they were chlorpyrifos and diazinon. At the river upstream where a dam is located for public water supply, incidents of pesticide levels exceeding the European Economic Community Directive of water quality standards have occurred. Furthermore, the wetland ecosystems located at the downstream of the river which houses the fireflies community is being threatened by occasional pesticide levels above EPA limits for freshwater aquatic organisms. The occurrence of these residual pesticides in the Selangor River can be attributed to the intense agriculture and urban activity.     

Comparison of phenanthrene biodegradation by free and immobilized cell systems: formation of hydroxylated compounds

One of the foremost environmental issues having a key role in the feasibility study of polycyclic aromatic hydrocarbons (PAHs) biodegradation is the concern of the toxicity of the formed intermediate metabolites. In this study, biodegradability of phenanthrene (PHE) at initial concentrations of 100–500 ppm and its hydroxylated intermediate metabolites (IMs) in aqueous phase were investigated using free cells (FC) and immobilized cells (IC) in polyvinyl alcohol (PVA) cryogel beads. Results showed that both FC and IC systems were capable of complete PHE biodegradation at initial concentrations lower than 250 ppm after 7 days, though IC system showed a higher PHE removal rate. The maximum IM concentrations observed at initial PHE concentrations of 100 and 250 ppm were 20 and 49 ppm for FC system, whereas 7.4 and 19 ppm were obtained for IC system, respectively, and IMs were finally removed after 7 days. Similarly, at 500 ppm, IC system resulted in higher removal of PHE compared to FC system. However, during the 7-day period for FC system, IMs concentration rose up to 59 ppm, while for IC system, IMs concentration reaches a maximum at day 5 and thereafter it follows a negative rate. It was also shown that resorcinol as an indicator of hydroxylated aromatic metabolites at concentrations of 0–100 ppm can well be biodegraded by free and immobilized cell systems. No prohibition on PHE biodegradation could hence occur due to IMs formation. Additionally, stability of IC system was examined in repeated-batch cultures, showing the effective removal of PHE up to nine reuse cycles.     

Optimizing stabilization of waste-activated sludge using Fered-Fenton process and artificial neural network modeling (KSOFM,MLP)

Sludge management is a fundamental activity in accordance with wastewater treatment aims. Sludge stabilization is always considered as a significant step of wastewater sludge handling. There has been a progressive development observed in the approach to the novel solutions in this regard. In this research, based on own initially experimental results in lab-scale regarding Fered-Fenton processes in view of organic loading (volatile-suspended solids, VSS) removal efficiency, a combination of both methods towards proper improving of excess biological sludge stabilization was investigated. Firstly, VSS removal efficiency has been experimentally studied in lab-scale under different operational conditions taking into consideration pH [Fe²⁺]/[H₂O₂], detention time [H₂O₂], and current density parameters. Therefore, the correlations of the same parameters have been determined by utilizing Kohonen self-organizing feature maps (KSOFM). In addition, multi-layer perceptron (MLP) has been employed afterwards for a comprehensive evaluation of investigating parameters correlation and prediction aims. The findings indicated that the best proportion of iron to hydrogen peroxide and the optimum pH were 0.58 and 3.1, respectively. Furthermore, maximum retention time about 6 h with a hydrogen peroxide concentration of 1,568 mg/l and a current density of 650–750 mA results to the optimum VSS removal (efficiency equals to 81 %). The performance of KSOFM and MLP models is found to be magnificent, with correlation ranging (R) from 0.873 to 0.998 for the process simulation and prediction. Finally, it can be concluded that the Fered-Fenton reactor is a suitable efficient process to reduce considerably sludge organic load and mathematical modeling tools as artificial neural networks are impressive methods of process simulation and prediction accordingly.     

UV–visible light-activated Ag-decorated,monodisperse TiO2 aggregates for treatment of the pharmaceutical oxytetracycline

Noble metal Ag-decorated, monodisperse TiO₂ aggregates were successfully synthesized by an ionic strength-assisted, simple sol–gel method and were used for the photocatalytic degradation of the antibiotic oxytetracycline (OTC) under both UV and visible light (UV–visible light) irradiation. The synthesized samples were characterized by X-ray diffraction analysis (XRD); UV–vis diffuse reflectance spectroscopy; environmental scanning electron microscopy (ESEM); transmission electron microscopy (TEM); high-resolution TEM (HR-TEM); micro-Raman, energy-dispersive X-ray spectroscopy (EDS); and inductively coupled plasma optical emission spectrometry (ICP-OES). The results showed that the uniformity of TiO₂ aggregates was finely tuned by the sol–gel method, and Ag was well decorated on the monodisperse TiO₂ aggregates. The absorption of the samples in the visible light region increased with increasing Ag loading that was proportional to the amount of Ag precursor added in the solution over the tested concentration range. The Brunauer, Emmett, and Teller (The BET) surface area slightly decreased with increasing Ag loading on the TiO₂ aggregates. Ag-decorated TiO₂ samples demonstrated enhanced photocatalytic activity for the degradation of OTC under UV–visible light illumination compared to that of pure TiO₂. The sample containing 1.9 wt% Ag showed the highest photocatalytic activity for the degradation of OTC under both UV–visible light and visible light illumination. During the experiments, the detected Ag leaching for the best TiO₂-Ag photocatalyst was much lower than the National Secondary Drinking Water Regulation for Ag limit (0.1 mg L^?1) issued by the US Environmental Protection Agency.     

Pesticide residues in fruits and vegetables from Pakistan: a review of the occurrence and associated human health risks

The main objective of the review is to document, assess and analyze the results of the previously reported data on levels of different pesticides in selected fruits and vegetables from Pakistan. The findings of the previous studies clearly indicated that more than 50 % of the samples were contaminated with organophosphate, pyrethroids and organochlorine pesticides. Many studies reported that among fresh fruits and vegetables tomato, apple, melon, mango, grapes, and plum crossed the FAO/WHO permissible limits for these contaminants residual levels. The comparison of other regions showed that observed levels were found above maximum residue limits (MRLs) in 50 % of the samples but were in agreement with the studies from neighboring countries like China and Bangladesh. Higher hazard risk index (HRI) values were calculated for dieldrin, methamidophos, o,p′-DDT, diazinon and p,p′-DDT in apple, mango, banana, melon, potato and onion. The review also highlights that data on pesticide residues in foodstuff is scarce which should be overcome by further extending studies from different areas of Pakistan. In order to ascertain the provision of food suitable for human consumption, it is imperative to monitor pesticides in food commodities by the country’s authorities and enforce guidelines based on permissible limits.     

Analyzing the Variability of Remote Sensing and Hydrologic Model Evapotranspiration Products in a Watershed in Michigan

The goal of this paper was to statistically explore the spatiotemporal performance of remotely sensed actual evapotranspiration (ETa) datasets and a remotely sensed ensemble in a region that lacks observed data. The remotely sensed datasets were further compared with ETa results from a physically based hydrologic model (Soil and Water Assessment Tool) to examine the differences and determine the level of agreement between the ETa datasets and the model outputs. ETa datasets were compared on temporal (i.e., monthly and seasonal basis) and spatial (i.e., landuse) scales at both watershed and subbasin levels. The results showed a lack of consistent similarities and differences among the datasets when evaluating the monthly ETa variations; however, the seasonal aggregated data presented more consistent similarities and differences during the spring and summer compared to the fall and winter. Meanwhile, spatial analysis of the datasets showed the MOD16A2 500 m ETa product was the most versatile of the tested datasets, being able to differentiate between landuses during all seasons. Furthermore, the use of an averaging ensemble was able to improve overall ETa performance in the study area. This study showed that the remotely sensed ETa products are not similar throughout the year, but the appropriate application periods for different ETa products were identified. Finally, spatial variabilities of the ETa products are more in tune with landuse and climate characteristics.