环草隆与重金属复合污染对黄瓜及小麦的毒性效应评估

为探究草坪除草剂与重金属复合污染对高等植物的生态毒性效应,以小麦与黄瓜为敏感受试植物,采用滤纸发芽试验法,研究了典型草坪除草剂环草隆与4种重金属(Cu/Zn/Pb/Cd)单一及复合污染条件下,对2种植物种子萌发与幼苗生长的毒性效应并进行评估。在此基础上采用评估因子法外推环草隆在土壤中的预测无效应浓度(PNECsoil)。结果表明,2种植物的根长及小麦的芽长对环草隆与重金属非常敏感(P<0.01),且存在明显的剂量-效应关系。黄瓜根长对环草隆最敏感,根长半抑制浓度(RI50)为0.281 mg·L-1。小麦根长对Cu、Pb、Cd比黄瓜根长更敏感。环草隆与重金属复合污染时,黄瓜根长表现得最为敏感,可作为敏感生物标记物。环草隆与重金属复合污染对小麦及黄瓜根长抑制具有协同作用,并且随着重金属浓度的增大,黄瓜和小麦根生长对环草隆的敏感性增加。环草隆与重金属复合污染对小麦芽长的联合效应主要与重金属种类及其暴露浓度有关。以黄瓜的根伸长抑制率为急性毒性终点,利用外推法计算得环草隆在土壤中的PNECsoil为1.90μg·kg~(-1),远远低于环草隆田间推荐使用量1.5~9 mg·kg~(-1)。与重金属复合污染时,环草隆的PNECsoil明显降低,导致其生态风险提高。上述研究结果能够为草坪除草剂环草隆与重金属复合污染的生态风险评价提供数据支持。     

中国典型河湖水体铅的水生生物安全基准与生态风险评价

采用物种敏感度排序法(SSR)对我国铅的淡水水生生物安全基准进行推导,并以太湖为例进行了流域水生生物安全基准推导。对于难以获得的本土生物毒性数据,开展了相应的毒性试验。获得了我国国家与太湖流域铅的水生生物安全基准值,基准最大浓度(CMC)分别为63.92、104.26μg·L-1,基准连续浓度(CCC)分别为1.21、4.06μg·L-1。同时,对我国主要河流以及太湖流域进行了铅的生态风险评价,联合概率曲线法显示影响5%水生生物种类的概率分别为66.22%和43.19%,熵值法则显示中国主要河流存在较大的铅暴露风险,因此,我国铅的潜在生态风险较大,主要河流与太湖流域存在铅污染问题。     

Carbon dioxide emissions from cities in China based on high resolution emission gridded data

Based on the China high resolution emission gridded data (1 km spatial resolution), this article is aimed to create a Chinese city carbon dioxide (CO₂) emission data set using consolidated data sources as well as normalized and standardized data processing methods. Standard methods were used to calculate city CO₂ emissions, including scope 1 and scope 2. Cities with higher CO₂ emissions are mostly in north, northeast, and eastern coastal areas. Cities with lower CO₂ emissions are in the western region. Cites with higher CO₂ emissions are clustered in the Jing-Jin-Ji Region (such as Beijing, Tianjin, and Tangshan), and the Yangtze River Delta region (such as Shanghai and Suzhou). The city per capita CO₂ emission is larger in the north than the south. There are obvious aggregations of cities with high per capita CO₂ emission in the north. Four cities among the top 10 per capita emissions (Erdos, Wuhai, Shizuishan, and Yinchuan) cluster in the main coal production areas of northern China. This indicates the significant impact of coal resources endowment on city industry and CO₂ emissions. The majority (77%) of cities have annual CO₂ emissions below 50 million tons. The mean annual emission, among all cities, is 37 million tons. Emissions from service-based cities, which include the smallest number of cities, are the highest. Industrial cities are the largest category and the emission distribution from these cities is close to the normal distribution. Emissions and degree of dispersion, in the other cities (excluding industrial cities and service-based cities), are in the lowest level. Per capita CO₂ emissions in these cities are generally below 20 t/person (89%) with a mean value of 11 t/person. The distribution interval of per capita CO₂ emission within industrial cities is the largest among the three city categories. This indicates greater differences among per capita CO₂ emissions of industrial cities. The distribution interval of per capita CO₂ emission of other cities is the lowest, indicating smaller differences of per capita CO₂ emissions among this city category. Three policy suggestions are proposed: first, city CO₂ emission inventory data in China should be increased, especially for prefecture level cities. Second, city responsibility for emission reduction, and partitioning the national goal should be established, using a bottom-up approach based on specific CO₂ emission levels and potential for emission reductions in each city. Third, comparative and benchmarking research on city CO₂ emissions should be conducted, and a Top Runner system of city CO₂ emission reduction should be established.     

A Two-Stage Particle Swarm Optimization Algorithm for MPPT of Partially Shaded PV Arrays

The power-voltage (P-V) characteristic curves of a PV array are nonlinear and have multiple peaks under partially shaded conditions (PSCs). This paper proposes a novel maximum power point tracking (MPPT) method for a PV system with reduced steady-state oscillation based on a two-stage particle swarm optimization (PSO) algorithm. The grouping method of the shuffled frog leaping algorithm (SFLA) is incorporated in the basic PSO algorithm (PSO-SFLA), ensuring fast and accurate searching of the global extremum. An adaptive speed factor is also introduced into the improved PSO to further enhance its convergence speed. Test results show that the proposed method converges in less than half the time taken by the conventional PSO method, and the power is improved by 33% under the worst PSCs, which confirms the superiority of the proposed method over the standard PSO algorithm in terms of tracking speed and steady-state oscillations under different PSCs.     

粉末活性炭对三烯丙基异氰脲酸酯的吸附性能简

用静态吸附法考察粉末活性炭对水中三烯丙基异氰脲酸酯（CAIC）的吸附行为,采用单因素分析法对活性炭吸附化工废水中TAIC的工艺条件进行研究。实验结果表明,在TAIC模拟废水中,其TAIC初始浓度为800 mg/L,pH为7,在温度为298 K、转速为150 r/min的条件下,当活性炭的投加量达到4.4 g/L,吸附反应时间为50 min时,TAIC的去除效率最高为96.17%;对于实际废水,其TAIC初始浓度为1 500 mg/L,溶液pH为3,在温度为298 K、转速为150 r/min的条件下,当活性炭投加量达到10 g/L,吸附反应时间为2 h时,TAIC的去除效率最高为46.8%。这也是由于实际废水组分复杂,其他有机物存在一定的吸附竞争机制。     

添加炭基材料对蔬菜废物好氧堆肥进程和腐熟度的影响

以蔬菜废弃物辣椒秸秆和树叶为堆肥原料(CK),采用密闭式好氧堆肥工艺,研究了添加5%木本泥炭(T1)、5%活性炭(T2)和10%木本泥炭(T3)等炭基材料对堆肥p H、EC、CO2累积量、物料损失率、T值、C/N和发芽率指数的影响。结果显示,T2处理的p H在60 d后维持在8~9之间;EC值随着堆肥进行呈现先下降后升高再下降的趋势,最终CK、T1、T2和T3处理的EC值(m S/cm)分别降低了1.02、0.76、0.33和0.48;T2和T3处理的CO2累积量一直高于其他处理;所有处理的物料损失率均在20%以上;4个处理堆肥产品的T值分别为0.56、0.65、0.68和0.69;堆肥产品的发芽率指数分别为63.2%、69.3%、93.5%和86.1%。T值和发芽率指数显示T2和T3处理达到了腐熟阶段。结果表明,在蔬菜堆肥处理中添加炭基材料可改善堆肥产品的理化性质,加速堆肥物料的分解,有效地缩短堆肥周期和提高堆肥产品的腐熟度。     

Comparison of lignin peroxidase and horseradish peroxidase for catalyzing the removal of nonylphenol from water

Concentrations of aqueous-phase nonylphenol (NP), a well-known endocrine-disrupting chemical, are shown to be reduced effectively via reaction with lignin peroxidase (LiP) or horseradish peroxidase (HRP) and hydrogen peroxide. We systematically assessed their reaction efficiencies at varying conditions, and the results have confirmed that the catalytic performance of LiP toward NP was more efficient than that of HRP under experimental conditions. Mass spectrum analysis demonstrated that polymerization through radical–radical coupling mechanism was the pathway leading to NP transformation. Our molecular modeling with the assistance of ab initio suggested the coupling of NP likely proceeded via covalent bonding between two NP radicals at their unsubstituted carbons in phenolic rings. Data from acute immobilization tests with Daphnia confirm that NP toxicity is effectively eliminated by LiP/HRP-catalyzed NP removal. The findings in this study provide useful information for understanding LiP/HRP-mediated NP reactions, and comparison of enzymatic performance can present their advantages for up-scale applications in water/wastewater treatment.     

Manganese concentrations in maternal–infant blood and birth weight

Manganese (Mn) is an essential mineral nutrient in mammals. The physiological role of Mn in animal models is well documented, but little is known about the adverse effects of Mn deficiency or overexposure in humans, including pregnancy outcomes such as birth weight. We examined the relationship of the maternal and cord blood Mn levels with birth weight in a cohort of 172 mother–infant pairs born in Shanghai, China. Non-linear spline and quadratic regression models were used to test the hypothesis of an inverted U-shaped association between the Mn levels and birth weight. The median (range) levels of Mn in the maternal and cord blood were 5.38 (2.34–30.37) μg/dL and 7.66 (2.57–34.23) μg/dL, respectively. An inverted U-shaped relationship was observed between maternal Mn and birth weight after adjusting for potential confounders. The birth weight increased with Mn levels up to 4.18 μg/dL, and a slight reduction in weight was observed at higher levels. The cord blood Mn levels were not found to be associated with birth weight. Both lower and higher Mn exposures are associated with lower birth weight, which may influence important developmental parameters; the association of higher Mn levels with lower weight was weak and imprecise.     

Fate in soil of 14C-sulfadiazine residues contained in the manure of young pigs treated with a veterinary antibiotic

The fate of ¹⁴C-labeled sulfadiazine (¹⁴C-SDZ) residues was studied in time-course experiments for 218 days of incubation using two soils (A_p horizon of loamy sand, orthic luvisol; A_p horizon of silt loam, cambisol) amended with fresh and aged (6 months) ¹⁴C-manure [40 g kg^?1 of soil; 6.36 mg of sulfadiazine (SDZ) equivalents per kg of soil], which was derived from two shoats treated with ¹⁴C-SDZ. Mineralization of ¹⁴C-SDZ residues was below 2% after 218 days depending little on soil type. Portions of extractable ¹⁴C (ethanol-water, 9:1, v/v) decreased with time to 4–13% after 218 days of incubation with fresh and aged ¹⁴C-manure and both soils. Non-extractable residues were the main route of the fate of the ¹⁴C-SDZ residues (above 90% of total recovered ¹⁴C after 218 days). These residues were high immediately after amendment depending on soil type and aging of the ¹⁴C-manure, and were stable and not remobilized throughout 218 days of incubation. Bioavailable portions (extraction using CaCl₂ solution) also decreased with increasing incubation period (5–7% after 218 days). Due to thin-layer chromatography (TLC), 500 μg of ¹⁴C-SDZ per kg soil were found in the ethanol-water extracts immediately after amendment with fresh ¹⁴C-manure, and about 50 μg kg^?1 after 218 days. Bioavailable ¹⁴C-SDZ portions present in the CaCl₂ extracts were about 350 μg kg^?1 with amendment. Higher concentrations were initially detected with aged ¹⁴C-manure (ethanol-water extracts: 1,920 μg kg^?1; CaCl₂ extracts: 1,020 μg kg^?1), probably due to release of ¹⁴C-SDZ from bound forms during storage. Consistent results were obtained by extraction of the ¹⁴C-manure-soil samples with ethyl acetate; portions of N-acetylated SDZ were additionally determined. All soluble ¹⁴C-SDZ residues contained in ¹⁴C-manure contributed to the formation of non-extractable residues; a tendency for persistence or accumulation was not observed. SDZ's non-extractable soil residues were associated with the soluble HCl, fulvic acids and humic acids fractions, and the insoluble humin fraction. The majority of the non-extractable residues appeared to be due to stable covalent binding to soil organic matter.     

Preliminary study on removing Cs+/Sr2+ by activated porous calcium silicate—A by-product from high-alumina fly ash recycling industry

¹³⁷Cs⁺/⁹⁰Sr²⁺-containing radioactive wastewater is one of the most important problems that the world has been facing with. A by-product, activated porous calcium silicate, is generated at high levels by the pre-desiliconizing and soda-lime-sintering processes for producing Al₂O₃ from high-alumina fly ash. In order to examine if this by-product could be used as an absorbent for removal of ¹³⁷Cs⁺/⁹⁰Sr²⁺ from radioactive wastewater, various parameters, such as pH, adsorbent dose, contact time, and initial concentration, were discussed. Results indicated that the equilibrium reached in about 2 hr. Activated porous calcium silicate was highly pH sensitive and able to remove Cs⁺/Sr²⁺ in a near-neutral environment. The adsorption equilibrium was best described by Freundlich isotherm equations, and the adsorption of Cs⁺/Sr²⁺ was a physical process. The adsorption kinetic data could be better fitted by the pseudo-second-order model, and the adsorption was controlled by multidiffusion. Current study showed that activated porous calcium silicate has a good adsorption of Cs⁺/Sr²⁺ for their removal. However, other characteristics, such as selectivity because of coexisting cations, elution and regeneration, thermal stability, and acid resistance, should be discussed carefully before using it in an actual field.

Implications:Removing ¹³⁷Cs⁺/⁹⁰Sr²⁺ from radioactive wastewater is one of the tough issues that has been attracting more and more attention world widely, which is the same as fly ash. For recycling high-alumina fly ash, in which Al is extracted to produce Al₂O₃, a huge amount of activated porous calcium silicate is generated year by year. In this paper, this by-product was successfully used as an absorbent to remove ¹³⁷Cs⁺/⁹⁰Sr²⁺ from radioactive wastewater for the first time. Factors that affect the absorbability and the mechanisms were discussed in details, providing a possible choice for disposal of ¹³⁷Cs⁺/⁹⁰Sr²⁺-containing radioactive wastewater.