塔里木河流域适应气候变化和人类活动的应对措施

自2001年开始实施塔里木河流域近期综合治理工程,提出了以强化流域水资源统一管理和调度为核心,以源流区节水改造和干流河道治理为重点进行综合治理,积极稳妥地进行经济结构调整,实施退耕封育保护,有效保护好现有天然林草植被.通过向塔里木河下游生态输水,干涸近30a的台特玛湖于2001年11月16日开始有水,使塔里木河下游绿色走廊得到初步复苏等,流域生态环境得到极大的恢复.然而,自2007年以来,塔里木河向下游输水已大为减少,仅能输水到中游,特别是2009年水文干旱,塔里木河干流断流达1 100km多,使下游绿色走廊再度陷入生态危机.为此,需要重新审视塔里木河流域的综合治理,从加强源流治理开始,来巩固干流治理成果.认真总结10a来治理经验与教训,针对人类活动和气候变化对源流与干流造成的影响程度,积极采取应对措施.     

电气石矿物吸附铜离子试验研究

本文研究了电气石的单晶、电气石微粉对Cu2＋的吸附作用,试验表明：电气石单晶体表面存在着以C轴为两极的静电场,该静电场对Cu2＋的吸附作用效果明显。制备的电气石微粒越细,吸附效果越好。电气石的电场效应使得它在治理污水中Cu2＋污染具有广阔的前景。     

高亚硝酸盐胁迫下日本囊对虾肝胰腺的转录组分析

海岸带盐度过渡区域水体中氮、磷的准确测定对陆海统筹及海岸带管理起着至关重要的作用。为探究盐度对氮、磷测定准确度的影响,进而明确河口海岸带淡水-咸水盐度过渡区不同形式氮、磷测定方法的选择依据,分别采用淡水和海水的相关国家标准方法,测定不同盐度下不同质量浓度氮、磷的人工海水和天然海水水样中氨氮、亚硝氮、总氮、活性磷酸盐和总磷的质量浓度。结果表明,盐度对某些氮、磷的淡水法和海水法测定结果有一定程度的影响。对氨氮的测定,当S≤4.0时淡水法或海水法均可准确测定水体中的氨氮,S>4.0时应对水样进行pH 调整预处理后用海水法进行测定;对亚硝氮的测定,淡水法和海水法的测定结果无明显差异;对总氮的测定,当S≤5.0时应采用操作简单、测定准确的淡水法测定,S>5.0时应采用海水法。对水体中的活性磷酸盐的测定,在低盐低磷(S≤35.0且ρPO3-4 ≤0.2mg·L-1)的情况下盐度对淡水法和海水法测定结果的影响微乎其微,而对于高盐高磷(S>35.0且ρPO3-4 > 0.2mg·L-1)的水样选择灵敏度更高的海水法测定更准确;对总磷的测定,选取海水法测定准确度更高。研究结果为海岸带水体不同形式氮、磷质量浓度的准确测定与方法选择提供了科学依据。     

重金属胁迫对两种海洋饵料微藻的急性毒性效应研究

在模拟生态环境条件下研究了铜(Cu2+)、镉(Cd2+)和锌(Zn2+)3种重金属离子对2种海洋饵料微藻(青岛大扁藻(Platymonas helgolandica)和等鞭金藻8701(Isochrysis galbana 8701))的急性毒性效应,分析其对种群增长的影响,并利用透射电镜对微藻亚显微结构的变化进行分析。在实验浓度范围内,2种微藻的种群增长对3种重金属离子的急性胁迫表现出类似的变化趋势,随着胁迫浓度的增加,微藻的相对增长率均呈现出不断下降的趋势;通过比较2种微藻的48hEC50和96h-EC50发现:3种重金属离子的毒性程度为Cu2+Cd2+Zn2+,等鞭金藻8701对重金属胁迫的敏感性高于青岛大扁藻。2种微藻的亚显微结构观察显示,二者的膜结构及细胞核对Cu2+胁迫并不太敏感;与对照组相比等鞭金藻8701的色素体及贮能物质受影响较严重,而青岛大扁藻的叶绿体及淀粉粒受影响较大。     

一株海洋微藻的分离鉴定及其产油条件优化

自青岛近岸海水中分离到一株硅藻,经形态学和分子生物学鉴定,表明该藻与小头菱形藻(Nitzschia microcephala)最为相近,18SrDNA相似性99%以上。研究以f/2培养基为基础,对该藻的生长和油脂积累条件进行探析,表明其在pH=6~8时具有较高的生长速率,最大可达到0.01d-1,油脂含量随pH的升高而降低;添加SiO2-3可以抑制菱形藻的生长和油脂积累;高浓度的Fe3+能促进菱形藻的生长;在Zn2+浓度为1.74μmol/L的条件下,菱形藻能够较好地生长并且进行油脂的积累;其中pH、SiO2-3和Fe3+是影响该藻生长和油脂积累的主要因子。正交试验研究表明,该藻在f/2培养液中生长和油脂积累的最优条件为初始pH=9,SiO2-3和Fe3+添加浓度分别为0.07和100μmol/L。在该最优条件下,该藻的生物量和油脂积累可分别达到94.7mg/L和19.6%。     

Measurement of trace nitrate concentrations in seawater by ion chromatography with valve switching

An ion chromatographic method with a valve switching facility was developed to determine trace nitrate concentrations in seawater using two pumps, two different suppressors, and two columns. A carbohydrate membrane desalter was used to reduce the high concentrations of sodium salts in samples. In this method, trace nitrate was eluted from the concentrator column to the analytical columns, while the matrix flowed to waste. Neither chemical pre-treatment nor sample dilution was required. In the optimized separation conditions, the method showed good linearity （R〉0,99） in the 0.05 and 50 mg/L concentration range, and satisfactory repeatability （RSD〈5%, n=6）. The limit of detection for nitrate was 0.02 mg/L. Results showed that the valve switching system was suitable and practical for the determination of trace nitrate in seawater.     

羟基磷灰石对水溶液中Fe3+的吸附动力学及热力学研究

研究了羟基磷灰石(HAP)对水溶液中Fe3+的吸附动力学及热力学。研究表明,HAP对水溶液中Fe3+的吸附符合Langmiur等温吸附,ct/q=0.006 4 ct+0.018 3;该吸附反应符合一级反应动力学方程,ln CR=-0.043 5 t+4.324 4;吸附反应活化能为Ea=36.26 k J/mol;标准摩尔反应焓为正值表明反应过程吸热;当温度大于285.7 K时,吉布斯自由能小于0,反应可自发进行。     

Lithium Ion Extraction from the High Ration Mg/Li Salt Lake Brine with Ionic Liquid in Triisobutyl Phosphate and Kerosene

正1 Introduction As the lightest metal with the unique properties of energy production and storage,lithium is regarded as the new century energy metal.Lithium and its compounds were widely used in various industrial fields,especially in     

Geochemical and isotopic evidence of a groundwater source in the Corral Canyon meadow complex,central Nevada,USA

Major inorganic ions and stable carbon and oxygen isotopes in stream water, groundwater, groundwater seeps and springs were measured in the Corral Canyon meadow complex and watershed in the Toquima Mountains of central Nevada, USA. The purpose of the study was to determine whether stream water or groundwater was the source of water that supports vegetation in the meadow complex. Water samples from the watershed and meadow complex were mixed cation–HCO₃ type. Stream water sampled at different locations in the meadow complex showed variations in temperature, pH and specific conductance. The cation–anion proportions for stream water were similar to groundwater, groundwater seeps and runoff from the meadow complex. Stable oxygen isotope ratios for stream water (?17·1 to ?17·6‰ versus VSMOW) and groundwater and groundwater seeps in the meadow site (?17·0 to ?17·7‰ versus VSMOW) were similar, and consistent with a local meteoric origin. Dissolved inorganic carbon (DIC) and the δ ¹³C_DIC for stream water (?12·1 to ?15·0‰ versus VPDB) were different from that of groundwater from the meadow complex (?15·3 to ?19·9‰ versus VPDB), suggesting different carbon evolution pathways. However, a simple model based on cation–δ ¹³C_DIC suggests that stream water was being recharged by shallow groundwater, groundwater seeps and runoff from the meadow complex. This leads to the conclusion that the source of water that supports vegetation in the meadow complex was primarily groundwater. The results of this study suggest that multiple chemical and stable carbon isotope tracers are useful in determining the source of water that supports vegetation in meadow complexes in small alpine watersheds. Copyright © 2004 John Wiley & Sons, Ltd.     

EFFECTS OF COMPOSITION AND STRUCTURE OF ALGINATES ON ADSORPTION OF DIVALENT METALS

Results of a series of experiments(on the adsorption of divalent metal ions by dried alginic acid, Na and Ca alginates of different composition and block structure) conducted in this systematic study of the effects of the composition and structure of alginates on the static adsorption equilibrium of divalent metal ions indicate that the properties of alginate adsorption to divalent metal ions are highly different, depending not only on the cations used, but also on the form and structure of the alginates. There is close correlation between the adsorption properties and the structure of the alginates. The selectivity coefficient of Na alginate for Cd-Sr ion exchange tends to increase with the increase of the M/G ratio in alginate, whereas the adsorption capacity of Ca alginate for Cu~(2+) ion decrease with the increase of the G-block or the average length of the G-block ((?)_G) and the total adsorption capacity of alginic acid is found to vary in the same order as the F_(MM)(diad frequency) in alginate in