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.     

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)     

介质阻挡放电降解环境污染物CF2ClBr的等离子体系电子密度

在利用介质阻挡放电对污染物质ＣＦ２ＣｌＢｒ进行等离子体降解产物分析的基础上,进一步研究等离子体系中的电子密度。采用动态反应装置,以平行板电极法直接测量。在ＣＦ２ＣｌＢｒ的压力为２ｋＰａ时,得出该实验条件下的电子密度约为５．０×１０＾１３／ｍ＾３。     

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.     

沸石对降雨径流中氨氮的吸附特性

城市面源污染是重要水体污染源之一,降雨发生时,雨水径流会携带累积在路面、屋面的含有机物、氮磷、重金属等污染物质进入水体,其中氮磷是造成水体富营养化的重要因素。针对这一情况,采用不同种类沸石,对雨水径流中的氮磷进行了吸附研究,着重考察了沸石对氨氮的吸附动力学,吸附等温线特征,并考察了pH、共存阳离子以及COD对吸附能力的影响。结果表明,Na型改性沸石吸附性能优于其他2种,饱和吸附量达到9.09 mg/g,沸石的吸附过程符合准二级动力学模型。Mg2+、Ca2+对Na型改性沸石的影响较大,Na型改性沸石吸附氨氮的适宜pH为5~8。本研究为探索用物化方法来处理雨水提供了依据,Na型改性沸石可以作为吸附雨水中氨氮的优选吸附剂。     

Fe3O4-TiO2Al吸附剂去除水中氟离子

以实验室制备的Fe3O4-TiO2·nH2O·Al吸附剂处理模拟和实际含氟废水,探讨了吸附剂用量、体系pH、吸附温度和吸附时间等因素对F-吸附效果的影响。结果表明:在初始F-浓度16.1 mg/L,起始pH 8.0,吸附剂投加量5 g/L,室温(约25 ℃)下吸附15 min时,模拟和实际废水的出水F-均可达到3O4-TiO2·nH2O·Al具有一定的实际应用价值。含氟水溶液初始pH对Fe3O4-TiO2·nH2O·Al吸附F-性能影响较大。在pH 介于3.0~5.0 时,吸附容量较大,过高或过低都会导致吸附容量降低。Fe3O4-TiO2·nH2O·Al吸附F-的过程为放热反应,升温不利于F-的吸附。该吸附剂吸附F- 的过程为化学吸附,符合准二级动力学模型,等温线拟合接近Freundlich吸附等温线。     

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.