乐昌Pb/Zn矿区水稻土中Pb的形态分布特征

对多年利用矿山废水灌溉的水稻土中Pb的化学形态、植物有效态和动物／人有效态进行了分析研究。结果表明，土壤中Pb的碳酸盐结合态、可交换态、有机结合态和Fe-Mn氧化物结合态含量分别是363、338、185和155mg／kg，其总和占总Pb含量的72．70％，表明其较高的环境敏感性；动物／人有效态Pb含量为1085mg／kg。土壤有机态Pb与植物中Pb含量相关性最高，表明用有机态表征土壤Pb的植物有效态比惯常使用的DTPA态要好。植物有效态与动物／人有效态含量相比，前者为后者的17．05％，表明土壤Pb污染对当地动物／人的潜在生态危害远远大于水稻等农作物；Fe-Mn氧化物结合态Pb与植物有效态（即有机结合态）及动物／人有效态Pb相关性最好，表明该形态对土壤Pb的生物有效性具有积极作用。     

土壤中钙、镁的形态分析及提取序列的研究

本文采用改进的BCR三步连续提取法对河北某食道癌高发地土壤中钙、镁进行了形态分析及提取序列的研究。实验表明：该地区土壤中镁主要以残渣态形式存在（占总量的83.66％-88.36％）,钙则受提取序列的影响很大,在第一提取序列中,以酸溶态为主（74.11％-83.38％）;第二提取序列中,以有机物结合态为主（78.12％-97.17％）;第三、四提取序列中,以氧化物结合态为主（87.49％-103％）。提取剂的加入顺序明显影响到钙的各个形态的真实含量。     

准噶尔盆地南缘荒漠与农牧区交错带土壤Cu、Pb化学形态分布特征

采取Tessier连续提取法,研究了荒漠与农牧区交错带土壤中Cu,Pb的化学形态分布。结果表明,荒漠与农牧区交错带土壤中Cu、Pb主要以残渣晶格态为主,可交换态比例较低。Cu(荒漠土壤样品除外)的各形态含量之间的相互关系为:残渣态>有机物结合态>铁锰氧化物结合态>碳酸盐结合态>可交换态。荒漠土壤样品中重金属Cu各形态含量之间的相互关系为:残渣态>铁锰氧化物结合态>有机物结合态>碳酸盐结合态>可交换态;重金属Pb各形态含量之间的相互关系为:残渣态>铁锰氧化物结合态>碳酸盐结合态>可交换态>有机物结合态。重金属Pb的活性态较高,高于重金属Cu的活性态。     

攀枝花市攀钢工业区土壤重金属污染特征及评价

本文对攀枝花市攀钢工业区土壤中五种重金属元素（Cu、Pb、Zn、Cr、Cd）的空间的分布特征、形态分布特征进行了研究，并应用污染负荷指数法对各重金属的污染程度进行了评价。研究发现，Cu、Pb、Zn、Cr的最大值与最小值分别相差2．98、3．4、5．2、2．7倍，cd的最大值与最小值甚至相差15．7倍。重金属元素相关性特征可分为Cd—Pb—Zn和Cu—Cr两组。形态分布特征表现在Cu、Zn、Pb、Cr主要以稳定的残渣态存在，Cd主要以可利用性最强的可交换态和碳酸盐结合态存在。污染较严重的是攀钢机关、攀钢原料场。     

辽宁省污灌区土壤重金属铜、铬、镉和汞的形态研究

文章采用Tessier连续提取+AAS和AFS法对辽宁省污灌区土壤中铜、铬、镉和汞4种重金属的形态进行分析。研究结果表明,辽宁省污灌区土壤中重金属铜、铬、镉和汞的全部高于背景值。铜和铬的各形态分布趋势为:残渣态有机态铁锰氧化态碳酸盐态可交换态,镉的各形态分布趋势为:可交换态残渣态有机结合态铁锰氧化物结合态碳酸盐结合态,汞的各形态分布趋势为:残渣态有机态铁锰氧化态碳酸盐态可交换态,但可交换态、碳酸盐态和铁锰氧化态的Hg含量很低,所占比例可忽略为0。     

城市污水强化生物除磷工艺中除磷菌种群结构分析

采用PCR-DGGE等分子生物学技术。从平行AN／AO工艺六个反应池的活性污泥样品中提取总DNA，采用套式PCR（nested PCR）进行两轮PCR扩增。对α-Proteobaeteria、β-Proteobacteria的16S rDNA片段进行DGGE（变性梯度凝胶电泳）分离，从而分析活性污泥样品中该类除磷菌的种群结构。结合测序技术并通过NCBI（美国国立生物技术信息中心）基因库比对，证实生物除磷过程中存在着丰富的α-Proteobacteria、β-Proteobacteria，同时可以得到其中优势类群的初步认识。结果表明，PCR-DGGE结舍测序技术可以用于污水处理过程中样品的除磷菌群落结构分析。     

宜宾兴文县僰王山镇水田土壤中硒形态分布特征及研究

为了客观分析土壤中硒形态分布特征及硒有效性影响因素,依据硒不同形态下的溶解度不同,采用四步五态连续浸提取技术,由弱到强的选择顺序提取僰王山镇水田土壤中硒的水溶态、可交换态、有机质结合态、硫化物/硒化物态、残渣态这5种形态,并用原子荧光光谱法分析和氢化物发生-原子荧光光谱法测定了土壤样品中5种形态硒和总硒的含量。初步总结了研究区水田土壤硒含量特征和硒形态分布特征。研究结果发现,僰王山镇水田土壤总硒含量变化范围为0.51~0.93 mg/kg,平均值0.714 mg/kg,远远超过全国土壤总硒平均值0.290 mg/kg,且超过了目前认为的富硒土壤的标准值0.4 mg/kg。从土壤中5种形态分析结果所占比例来看,有机质结合态和硫化物/硒化物态硒是硒元素的主要赋存形态,两者占土壤总硒含量的54.63%,反应了研究区土壤中硒富集与有机质结合态存在密切关系。     

钢渣吸附除磷性能的试验研究

研究了钢渣的吸附除磷效果并进行机理探讨。结果表明：钢渣采用0．5g,即可在25℃下、2个小时内,将100ml的磷浓度为10mg／L（以磷计）的模拟含磷废水的磷浓度降至0．5mg／L以下,达到磷的国家一级排放标准;钢渣吸附平衡时问为2小时;钢渣吸附除磷的机理主要是沉淀、吸附（表面络合反应）,并辅以静电作用。     

真,假草本咖啡种子的鉴别

在对草本咖啡（Ｃａｓｓｉａｓｏｐｎｅｒａｉｉｎｎ）、望江南（ＣａｓｓｉｓｏｃｃｉｄｅｎｔａｌｉｏＬ．）和决明（ＣａｓｓｉａｔｏｒａＬ．）种子的大小、颜色、形态进行了观察、研究，并对其形态特征进行了解剖学的分析后，提出了鉴别３种种子的方法。     

环境因子对长江宜宾段底泥吸附磷的影响

本文主要研究模拟长江底泥对富营养化水体磷的吸附,分析环境因子对底泥吸附磷的影响。结果显示：（1）在25℃时,底泥对磷的吸附在碱性条件时的吸附速率小于酸性和中性条件,中性条件下的吸附速率最大;（2）在控制上覆水温度时,温度越高底泥对磷的吸附量越小,20℃时底泥的吸附量是30℃吸附量的1.5倍;（3）上覆水中溶解氧的浓度越高,吸附速率越高。     

不同pH条件下沉积磷释放到水体中化学行为的模拟研究

通过室内模拟湖泊沉积物在不同pH条件下，研究释放到水体中各种磷形态的迁移转化行为，结果表明：碱性条件和酸性条件下，水体磷的时空变化由于其释放机制的不同，其迁移转化行为各不相同，同时，pH值的变化对水体中各种磷的相互转化没有明显的作用，各种磷形态的浓度变化，在很大程度上取决于水体中总磷的浓度。研究结果对认识沉积磷在环境条件变化时，磷在沉积物和水体体系中的迁移转化有重要的意义。     

湖泊内源磷的释放与富营养化的植物修复

阐述了磷形态的不同分类方法及磷的形态、水生生物、温度、pH值、溶解氧和扰动等因素对湖泊沉积层磷释放的影响,并对植物修复富营养化湖泊的机理和影响植物修复的环境因素进行了探讨和分析,指出在加强控制外源污染的同时,因地制宜,选择适宜的水生植物种类,对湖泊进行植物修复,逐步恢复湖泊的自然净化能力,可有效抑制湖泊富营养化。     

Speciation of phosphorus in phosphorus-enriched agricultural soils using X-ray absorption near-edge structure spectroscopy and chemical fractionation

Knowledge of phosphorus (P) species in P-rich soils is useful for assessing P mobility and potential transfer to ground water and surface waters. Soil P was studied using synchrotron X-ray absorption near-edge structure (XANES) spectroscopy (a nondestructive chemical-speciation technique) and sequential chemical fractionation. The objective was to determine the chemical speciation of P in long-term-fertilized, P-rich soils differing in pH, clay, and organic matter contents. Samples of three slightly acidic (pH 5.5-6.2) and two slightly alkaline (pH 7.4-7.6) soils were collected from A or B horizons in two distinct agrosystems in the province of Québec, Canada. The soils contained between 800 and 2100 mg total P kg(-1). Distinct XANES features for Ca-phosphate mineral standards and for standards of adsorbed phosphate made it possible to differentiate these forms of P in the soil samples. The XANES results indicated that phosphate adsorbed on Fe- or Al-oxide minerals was present in all soils, with a higher proportion in acidic than in slightly alkaline samples. Calcium phosphate also occurred in all soils, regardless of pH. In agreement with chemical fractionation results, XANES data showed that Ca-phosphates were the dominant P forms in one acidic (pH 5.5) and in the two slightly alkaline (pH 7.4-7.6) soil samples. X-ray absorption near-edge structure spectroscopy directly identified certain forms of soil P, while chemical fractionation provided indirect supporting data and gave insights on additional forms of P such as organic pools that were not accounted for by the XANES analyses.     

耐盐石油降解菌性能及降解条件优化

从冀东油田钻井废液中筛选分离出耐盐石油降解菌Virgibacillus sp.(简称SJ菌),其在高含盐条件下对石油具有较好的降解效果,高达56.12%左右。考察了pH值、盐度、不同N和P形态等因素对SJ菌降解石油效果的影响。结果表明:SJ菌有较宽的pH值适应范围(pH值为6～10)和较好的耐盐能力(0.5%～20%),在pH值为9及NaCl质量浓度为5%时对石油类降解效果最好,其最佳利用N源和P源分别为(NH2)2CO和KH2PO4,该研究为油田高含盐含油废液处理提供了一条新途径。     

Enzymatic hydrolysis of organic phosphorus in swine manure and soil

Organic phosphorus (Po) exists in many chemical forms that differ in their susceptibility to hydrolysis and, therefore, bioavailability to plants and microorganisms. Identification and quantification of these forms may significantly contribute to effective agricultural P management. Phosphatases catalyze reactions that release orthophosphate (Pi) from Po compounds. Alkaline phosphatase in tris-HCl buffer (pH 9.0), wheat (Triticum aestivum L.) phytase in potassium acetate buffer (pH 5.0), and nuclease P1 in potassium acetate buffer (pH 5.0) can be used to classify and quantify Po in animal manure. Background error associated with different pH and buffer systems is observed. In this study, we improved the enzymatic hydrolysis approach and tested its applicability for investigating Po in soils, recognizing that soil and manure differ in numerous physicochemical properties. We applied (i) acid phosphatase from potato (Solanum tuberosum L.), (ii) acid phosphatases from both potato and wheat germ, and (iii) both enzymes plus nuclease P1 to identify and quantify simple labile monoester P, phytate (myo-inositol hexakis phosphate)-like P, and DNA-like P, respectively, in a single pH/buffer system (100 mM sodium acetate, pH 5.0). This hydrolysis procedure released Po in sequentially extracted H2O, NaHCO3, and NaOH fractions of swine (Sus scrofa) manure, and of three sandy loam soils. Further refinement of the approach may provide a universal tool for evaluating hydrolyzable Po from a wide range of sources.     

EFFECT OF pH ON PHOSPHORUS RELEASE DURING MACROPHYTE (ELEOCHARIS sp.) DECOMPOSITION1

ABSTRACT: Laboratory microcosms were used to evaluate the effect of pH on release of soluble reactive phosphorus (SRP) during aerobic decomposition of the aquatic macrophyte Eleocharis sp., which is common in oligotrophic Florida lakes. The total amount of SRP released during a 227-day incubation in the dark was independent of pH over the range 3.7 to 5.5, but initial rates of release were faster at the lowest pH. The results indicate that the low total phosphorus concentrations observed in many acidic lakes are not necessarily attributable to reduced rates of decomposition and nutrient mineralization at low pH, as some researchers have suggested.     

Manure phosphorus extractability as affected by aluminum- and iron by-products and aerobic composting

Shifts in manure phosphorus (P) chemical forms and pool sizes induced by water treatment residuals and industrial mineral by-products are largely undefined. We conducted a manure P fractionation study to determine mechanisms of reduction of dissolved reactive phosphorus (DRP) in poultry manure upon mineral by-product additions. The effects of composting on the P immobilization efficacy of the by-products were determined using laboratory self-heating composting simulators. The mineral by-products included an aluminum-water treatment residual (Al-WTR) and an iron-rich titanium-processing by-product. The noncomposted manure averaged 0.11 g g(-1) of total P as DRP forms. The by-products significantly reduced manure DRP, by an average of 39 and 48% in the Al- and the Fe-treated manure, respectively. The by-products also reduced the 0.5 M NH4F-extractable phosphorus (FEP) fraction. Shifts in P forms between FEP and 0.1 M NaOH-extractable phosphorus (SHEP) depended upon the Al and Fe contents of the by-products while the combined FEP + SHEP pool remained constant. Phosphate sorption measurements supported the observations that the Fe-rich by-product was more effective at reducing manure DRP and enhancing the formation of SHEP forms at the expense of FEP than the Al-WTR. Composting had no effect on the efficacy of either by-product to reduce DRP. Potential mechanisms of enhanced P stabilization in treated manure upon composting included chemical shifts from the DRP and FEP fractions to the citrate-bicarbonate-dithionite extractable P fraction. Thus, the choice of P immobilization agents affected the stability of immobilized P forms and should be taken into consideration in developing manure processing and nutrient stabilization methods.     

内源磷的释放作用及影响因素研究进展

水体的富营养化已成为目前环境研究中的焦点问题,磷在湖泊中的浓度高低是衡量湖泊富营养化水平的重要指标,是水生态系统基本营养盐之一,并且是淡水湖泊的最主要限制性营养因子。在外源磷得到有效的控制之后,内源磷的污染仍然能够保持湖泊的富营养化状态,此时内源磷的控制就成为了难点和重点。在底泥中的结合态磷,主要是以无机磷和有机磷的形式存在,有机磷与微生物活性密切相关,无机磷则主要与底泥存在的环境联系紧密。湖泊底泥内源磷释放受到一系列物理、化学、生物过程的控制,其影响因素主要包括扰动、氧化还原电位、pH值等,是多种因子综合作用的结果,同时,扰动引起的底泥再悬浮对内源磷有吸附固定作用。故底泥内源磷的释放机理有待进一步探索,在多种影响因素作用下,进一步研究底泥再悬浮对磷的吸附释放作用,从而明确内源磷的主要来源及吸附释放过程,为内源磷的控制提供理论依据,进而控制水体富营养化。     

高压电化学絮凝技术去除酿酒废水中总磷的研究

为了使酿酒废水中总磷有效去除并达标排放,通过对酿酒废水总磷的排放情况调查,有针对性的选用高压电化学絮凝技术,对酿酒废水中总磷的去除效果进行实验研究。从实验结果看,调节进水pH值为2.3、停留时间45分钟时总磷去除率可达到99%以上,在该条件下COD的去除率也能达到50%左右,废水总磷排放浓度能够达到1.0mg/L的排放要求。     

Effect of reservoir flushing on downstream river water quality

The effect of short-term reservoir flushing on downstream water quality in the Geum River, Korea was studied using field experiments and computer simulations. The reservoir release was increased from 30 to 200 m(3)/s within 6 h for the purpose of this experiment. The flushing discharge decreased the concentrations of soluble nitrogen and phosphorus species considerably, but the experimental results revealed a negative impact on organic forms of nutrients and biochemical oxygen demand (BOD). A dynamic river water quality model was applied to simulate the river hydraulics and water quality variations during the event. The model showed very good performance in predicting the travel time of flushing flow and the variations of dissolved forms of nitrogen and phosphorus constituents. However, it revealed a limited capability in simulating organic forms of nutrients and BOD because it does not consider the re-suspension mechanism of these constituents from sediment during the wave front passage.