Interannual variation of ichthyoplankton density and species composition in the waters off northeastern Taiwan

The ichthyoplankton in the waters of northeastern Taiwan have been studied since 1989. Based on collections in August 1989 to 1991, this report treats primarily the annual variation of ichthyoplankton density, species composition and assemblage diversity among the waters of the East China Sea, the Kuroshio and the mixing zone. The ranges of average densities found for fish eggs were 7 to 3897 ind 1000 m^-3 and 0.02 to 1.43 g 1000 m^-3, for ichthyoplankton 154 to 1364 ind 1000 m^-3 and 0.33 to 3.23 g 1000 m^-3, and for zooplankton 52 to 532 g 1000 m^-3. An interannual comparison indicates a tendency towards a decrease in ichthyoplankton density from 1989 to 1991. In total, 5803 individuals assigned to at least 91 families and 254 taxa at species level were collected. Lantern fish form the most common species group (Benthosema pterotum: 12.1%; Diaphus pacificus: 4.2%). The other species in order of frequency are: gobies (5.8%); Callionymus sp. (3.4%); Auxis spp. (3.1%); Trachinocephalus myops (3.0%); Nibea sp. (2.8%); Synagrops philippinensis (2.3%); Priacanthus macracanthus (2.2%); and percophid (2.0%). The relative frequency of the ten most abundant taxa fluctuated annually. Neither interannual distinction nor interannual correlation was confirmed by statistical analysis, but intra-annual rank correlations were established among the water masses. A weak tendency towards increasing diversity from 1989 to 1990 and little diversity in the mixing zone were observed. We conclude that there is a complex inter-dependence of assemblages from the waters of northeastern Taiwan.     

活化过氧乙酸技术降解环境有机污染物的研究进展

近年来,以抗生素、内分泌干扰物等为代表的新污染物在环境中被频繁检出,对生态系统和人类健康构成潜在风险,高效稳定的有机污染物控制技术研发是当前环境领域的研究热点。以活化过氧乙酸的高级氧化技术为研究对象,对过渡金属、碳材料及其复合材料活化过氧乙酸的效果及其降解有机污染物的机制进行系统论述,重点探讨反应过程中的自由基（有机自由基、羟基自由基）和非自由基（单线态氧、高价金属氧物种、电子转移和表面络合的复合物）降解机制,总结了活化过氧乙酸技术在废水、土壤或沉积物、地下水等环境介质中对污染物的降解效果。提出了未来研究重点,即开发高效稳定的活化过氧乙酸催化剂,加强活化过氧乙酸技术在土壤和沉积物中降解有机污染物机制的探索,深入联合其他处理技术的应用研究。

     

Effects of long-term nitrogen addition and precipitation changes on CH4 flux in an alpine steppe北大核心CSCD

土壤是甲烷(CH4)重要的源和汇.氮沉降和降水格局变化正在急剧改变土壤碳循环,进而可能对土壤CH4通量造成深刻影响.高寒生态系统是巨大的碳库,对氮沉降和降水变化十分敏感.然而,目前多数研究集中在短期实验上,缺乏对长期氮沉降和降水变化背景下CH4通量的响应及其调控因素的认识.以青藏高原高寒草原为研究对象,在2013年搭建模拟氮沉降和降水格局改变实验平台.基于静态箱–气相色谱法测定2020年生长季(5-10月)土壤CH4通量.结果显示,高寒草原土壤呈CH4的汇.氮添加没有显著改变生长季和植物生长高峰CH4通量.然而,降水变化显著改变了生长季和植物生长高峰CH4通量,其中降水增加(+50%降水)降低了CH4的吸收(分别为–16%和–45%),降水减少(–50%降水)增强了CH4的吸收(分别为+73%和+33%).进一步研究发现,与植物属性和功能基因丰度相比,土壤环境因子主导了CH4通量变化(解释率>90%).其中CH4通量与土壤含水量和温度显著正相关,与土壤pH显著负相关.综上所述,在未来全球变化情景下,降水格局改变更能调节青藏高原高寒草原CH4通量的变化.(图6表1参37)     

Chlorinated and polycyclic aromatic hydrocarbons in riverine and estuarine sediments from Pearl River Delta, China

Spatial distribution of chlorinated hydrocarbons [chlorinated pesticides (CPs) and polychlorinated biphenyls (PCBs)] and polycyclic aromatic hydrocarbons (PAHs) was measured in riverine and estuarine sediment samples from Pearl River Delta, China, collected in 1997. Concentrations of CPs of the riverine sediment samples range from 12 to 158 ng/g, dry weight, while those of PCBs range from 11 to 486 ng/g. The CPs concentrations of the estuarine sediment samples are in the range 6-1658 ng/g, while concentrations of PCBs are in the range 10-339 ng/g. Total PAH concentration ranges from 1168 to 21,329 ng/g in the riverine sediment samples, whereas the PAH concentration ranges from 323 to 14,812 ng/g in the sediment samples of the Estuary. Sediment samples of the Zhujiang River and Macao harbor around the Estuary show the highest concentrations of CPs, PCBs, and PAHs. Possible factors affecting the distribution patterns are also discussed based on the usage history of the chemicals, hydrologic condition, and land erosion due to urbanization processes. The composition of PAHs is investigated and used to assess petrogenic, combustion and naturally derived PAHs of the sediment samples of the Pearl River Delta. In addition, the concentrations of a number of organic compounds of the Pearl River Delta samples indicate that sediments of the Zhujiang river and Macao harbor are most likely to pose biological impairment.     

Application of a constructed wetland for industrial wastewater treatment: a pilot-scale study

The main objective of this study was to examine the efficacy and capacity of using constructed wetlands on industrial pollutant removal. Four parallel pilot-scale modified free water surface (FWS) constructed wetland systems [dimension for each system: 4-m (L)x1-m (W)x1-m (D)] were installed inside an industrial park for conducting the proposed treatability study. The averaged influent contains approximately 170 mg l(-1) chemical oxygen demand (COD), 80 mg l(-1) biochemical oxygen demand (BOD), 90 mg l(-1) suspend solid (SS), and 32 mg l(-1) NH(3)-N. In the plant-selection study, four different wetland plant species including floating plants [Pistia stratiotes L. (P. stratiotes) and Ipomoea aquatica (I. aquatica)] and emergent plants [Phragmites communis L. (P. communis) and Typha orientalis Presl. (T. orientalis)] were evaluated. Results show that only the emergent plant (P. communis) could survive and reproduce with a continuous feed of 0.4m(3)d(-1) of the raw wastewater. Thus, P. communis was used in the subsequent treatment study. Two different control parameters including hydraulic retention time (HRT) (3, 5, and 7d) and media [vesicles ceramic bioballs and small gravels, 1cm in diameter] were examined in the treatment study. Results indicate that the system with a 5-d HRT (feed rate of 0.4m(3)d(-1)) and vesicles ceramic bioballs as the media had the acceptable and optimal pollutant removal efficiency. If operated under conditions of the above parameters, the pilot-plant wetland system can achieve removal of 61% COD, 89% BOD, 81% SS, 35% TP, and 56% NH(3)-N. The treated wastewater meets the current industrial wastewater discharge standards in Taiwan.     

Comparative study of extraction methods for the determination of PAHs from contaminated soils and sediments

The following four methods were compared on the extraction efficiency of 16 EPA (US Environmental Protection Agency) polycyclic aromatic hydrocarbons (PAHs): German method of the Verband Deutscher Landwirtschaftlicher Untersuchungs und Forschungsanstalten (VDLUFA), two methods of the International Organization for Standardization using shaking (ISO A) and Soxhlet extraction (ISO B) and an ultrasonic method. Recovery rates of 16 PAHs were determined in two soils. Extraction efficiency was evaluated in five soils and three sediments. Effect of drying soils and sediments on extraction efficiency was tested using the VDLUFA and the ultrasonic methods. Our study shows that the number of aromatic rings, rather than extraction procedures, significantly influenced recovery rates of individual PAHs. No significant differences in extraction efficiency of the four methods were observed for less polluted samples. For highly polluted soils, extraction efficiency decreased in the following order: VDLUFA method > ISO A > ultrasonic method > ISO B. Influence of soil moisture on extraction efficiency depended to some extent on both solvent used and content of PAHs in samples. A mixture of dichloromethane/acetone (5:1) is recommended for PAH extraction from moist samples when the ultrasonic method is used.     

Biodegradation of phthalate esters by two bacteria strains

In this study two aerobic phthalic acid ester (PAE) degrading bacteria strains, DK4 and O18, were isolated from river sediment and petrochemical sludge, respectively. The two strains were found to rapidly degrade PAE with shorter alkyl-chains such diethyl phthalate (DEP), dipropyl phthalate (DPrP), di-n-butyl phthalate (DBP), benzylbutyl phthalate (BBP) and diphenyl phthalate (DPP) are very easily biodegraded, while PAE with longer alkyl-chains such as dicyclohexyl phthalate (DCP) and dihexyl phthalate (DHP) and di-(2-ethylhexyl) phthalate (DEHP) are poorly degraded. The degradation rates of the eight PAEs were higher for strain DK4 than for strain O18. In the simultaneous presence of strains DK4 and O18, the degradation rates of the eight PAEs examined were enhanced. When the eight PAEs were present simultaneously, degradation rates were also enhanced. We also found that PAE degradation was delayed by the addition of nonylphenol or selected polycyclic aromatic hydrocarbons (PAHs) at a concentration of 1 microg/g in the sediment. The bacteria strains isolated, DK4 and O18, were identified as Sphigomonas sp. and Corynebacterium sp., respectively.     

Photocatalytic oxidation of triclosan

In the spring of 2003, there was an outbreak of the severe respiratory syndrome (SARS) in Hong Kong. Health concerns have thus triggered an increased and predominant use of various types of household cleansing agents such as triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol). However, it has been reported recently that triclosan could be photochemically converted to toxic 2,8-dichlorodibenzo-p-dioxin (2,8-Cl(2)DD) in the environment. It is therefore necessary to develop environmentally friendly methods for the treatment of triclosan. To this end, photocatalytic degradation of triclosan in aqueous solution was conducted using TiO(2) (Degussa P25) under irradiation of UV light (lambda < 365 nm). It was found that triclosan could be degraded by this approach. Hydrogen peroxide was added to enhance the degradation process, and the optimal initial hydrogen peroxide concentration for triclosan degradation was 0.005% (w/v). Product identification indicated that triclosan oxidation occurred at its phenol moiety and yielded quinone and hydroquinone intermediates. The formation of a dichlorophenol intermediate in triclosan degradation suggested bond-breaking of the ether linkage occurred during the process. Moreover, no chlorinated dibenzo-p-dioxin congener was detected. These findings confirm that the photocatalytic degradation of triclosan is an environmentally friendly process.     

On-road motor vehicle emissions and fuel consumption in urban driving conditions

This paper reports on the analysis of on-road vehicle speed, emission, and fuel consumption data collected by four instrumented vehicles. Time-, distance-, and fuel-based average fuel consumption, as well as CO, HC, NOx, and soot emission factors, were derived. The influences of instantaneous vehicle speed on emissions and fuel consumption were studied. It was found that the fuel-based emission factors varied much less than the time- and distance-based emission factors as instantaneous speed changed. The trends are similar to the results obtained from laboratory tests. The low driving speed contributed to a significant portion of the total emissions over a trip. Furthermore, the on-road data were analyzed using the modal approach. The four standard driving modes are acceleration, cruising, deceleration, and idling. It was found that the transient driving modes (i.e., acceleration and deceleration) were more polluting than the steady-speed driving modes (i.e., cruising and idling) in terms of g/km and g/sec. These results indicated that the on-road emission measurement is feasible in deriving vehicle emissions and fuel consumption factors in urban driving conditions.