萃取法分离回收不锈钢酸洗污泥硫酸浸出液中的重金属

采用非皂化P204和皂化P204萃取剂对不锈钢酸洗污泥的硫酸浸出液进行萃取。在浸出液pH为0.80、非皂化P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取时间为5 min的条件下,Fe~(3+)萃取率达99.64%,Cr~(3+)和Ni~(2+)萃取率为3.98%和6.99%,一次萃余液pH为0.64。采用皂化P204对除Fe~(3+)后的一次萃余液进行萃取,在P204体积分数为25%、萃取剂与浸出液体积比为1∶2、萃取剂皂化率为60%、一次萃余液pH为1.50、萃取时间为5 min的条件下,Ni~(2+)萃取率为93.12%,Cr~(3+)萃取率为20.69%,二次萃余液pH为2.63。     

亚磷酸盐降解微生物的筛选、鉴定和降解特性

从太湖底泥中筛选出一株能够利用亚磷酸盐(+3价)的细菌P1.通过生理生化实验及16S rDNA基因序列分析鉴定,P1菌与所有已知菌的同源性都很低,属于未知的新菌株.P1菌的最适培养条件为:pH6.5~7.0、温度30℃.P1菌能以亚磷酸盐为唯一磷源生长,在60~100mg P/L的初始亚磷酸盐培养条件下,100mgP/L的亚磷酸盐培养基中亚磷酸盐减少量最大(11%),培养基中生成正磷酸盐的比例最高1.6%.初始亚磷酸盐浓度越低,碱性磷酸酶(BAP)活性越高,60mgP/L的亚磷酸盐培养基中BAP的最高活性为1.86mol PNP/(L菌液·h).P1菌可能通过BAP将亚磷酸盐转化成生物体内所需的磷源.     

小头蓼(P.Microcephalum)对矿区铜的吸收积累研究

调查并分析云南省铜矿区的植物区系及土壤理化特性，发现小头蓼（P.Microcephalum）在云南省高海拔铜矿区生长旺盛，是该地区的优势植物种，小头蓼生长的土壤基质富含铜，其它养分条件适中，研究表明小头蓼具有较强的富集铜的能力；随土壤中铜含量的增加，植物根系铜含量也相应增加，但叶部铜含量变人与土壤铜含量之间无相关性，研究认为该植物具有对铜污染土壤的植物固定潜能。此外，还指出最适于小头蓼富集铜的土壤条件为土壤有机质1％－1.5％，土壤pH为中性。     

游离附生假单胞菌对铜绿微囊蓝细菌中32P释放的影响

采用同位素示踪法，分析游离附生假单胞菌(Pseudomonas sp-)对富集^32P的铜绿微囊蓝细菌(Microcystis aeruginosa)中磷释放的影响．研究结果表明：在微囊蓝细菌生长的延迟期和对数期．游离附生假单胞菌的加入抑制了微囊蓝细菌中^32P的释放，而对蓝细菌的生长没有明显的影响；在微囊蓝细菌生长的稳定期和衰减期，假单胞菌促进其蓝细菌细胞内^32P的释放，同时也加速微囊蓝细菌的衰亡．假单胞菌对微囊蓝细菌^32P释放的促进作用是由于自身的吸磷能力导致的．假单胞菌的吸磷量由假单胞菌生物量和细胞内磷浓度决定，假单胞菌在微囊蓝细菌的整个生长阶段生物量不断增加，而体内^32P浓度在开始阶段很低．直到微囊蓝细菌进入稳定期才达到相对稳定。     

P2P防污染机制的研究

文件污染是当前P2P文件共享系统普遍存在的问题,其中用户行为是导致污染的重要因素.在考察用户行为的基础上,建立了一个污染文件传播模型,描述了用户的污染意识、共享倾向等因素对污染传播的影响,并据此提出了相应的反污染机制.仿真实验表明,该机制能够有效地控制P2P文件共享系统中污染文件的传播.图6,表12.     

硅和磷配合施入对镉污染土壤的修复改良

为了研究两种改良剂配合施入对重金属污染土壤的改良效果,以棕壤为供试土壤,以玉米（OryzasativaL.）作为供试作物,采用二元二次正交回归组合设计方法,通过室外盆栽试验,研究了硅和磷配合施入对镉污染土壤中玉米生物量以及玉米茎叶中镉吸收量的影响。结果表明：硅、磷施入都能增加镉污染条件下玉米的生物量,其中磷的增产作用大于硅;硅、磷施入都能降低镉污染条件下玉米茎叶中的镉含量,硅降低玉米茎叶中镉含量的效应大于磷;硅、磷配合施入降低玉米茎叶中镉含量的效果大于上述两种改良剂单独施入。在本实验条件范围内,当硅为6.60g·kg-1,磷施入量范围在2.29～2.39g·kg-1时,玉米茎叶中镉含量为最低。因此可以由硅磷配合施入改良重金属污染的土壤。     

淹水对酸性红壤磷吸附解吸特性的影响——以江西省旱地红壤和水稻土为例

采用室内培养法研究了淹水对2种酸性红壤（旱地红壤、水稻土）磷吸附解吸特性及草酸可提取态P的影响。淹水培养实验中,2种土壤分别淹水0（对照）,1、2、3、4、8周,淹水培养结束后进行P吸附解吸实验,解吸实验结束后测定土样中草酸可提取态P。结果表明：与氧化状态相比,淹水后旱地红壤P吸附量减少,水稻土淹水1、2、3周P吸附量高于氧化状态,继续淹水4和8周后P吸附量减少。淹水前后旱地红壤P吸附量均大于水稻土。用简单Langmuir方程拟合P等温吸附曲线,除淹水4周外,P最大缓冲容量（MBC）随淹水时间延长而降低。结合能常数（K）淹水前后的变化规律性差。2种土壤P解吸量随加入P量增加而增加。氧化、还原状态下,2种土壤酸性草酸铵可提取P均远远大于CaCl2解吸P,虽然水稻土吸附P量低于旱地红壤,但P解吸量无论是CaCl2解吸P还是酸性草酸铵可提取P均大于旱地红壤,主要原因在于水稻土全P及速效P含量大于旱地红壤。淹水后草酸可提取态P增加,吸附P的释放和被新近形成的铁氧化物再吸附是淹水后草酸可提取态P增加的主要原因。     

Phosphorous cycling and biogeochemistry in a Venezuelan-flooded savanna

In 1970, a programme of land recuperation started in Venezuelan savannas, strongly affected by the seasonality of precipitation; therefore, a network of dykes has been built to alleviate the floods and retain water throughout the dry period. Under the dyked system, the environment has been altered, allowing a change in the herbaceous vegetation towards aquatic species and an increase in primary production. It is assumed that a considerable quantity of nutrients is lost from the ecosystem through the floodgates, a situation that could be worsened with the climate change. This contribution describes the atmospheric input and total output in stream run-off of phosphorous (P) in a flooded savanna. Internal pools of the biogeochemical cycle of P associated with terrestrial compartments are described. In the flooded savanna, a large amount of P is immobilised (29.6?kg?ha^?1) in their above ground biomass by grasses, and in soil microbial biomass. The P budget was nearly balanced, as measured losses were cancelled out by the inputs in rainfall. Soils act as a sink, retaining P coming either from precipitation or from desorption/mineralisation processes. That interruption can be maximised, and losses of P and other nutrients can be minimised with an adequate management of the floodgate.     

Research progress in microbial cytochrome P450 and xenobiotic metabolism北大核心CSCD

Cytochrome P450 (CYP450s) is a type of heme-mercaptide protein superfamily, which is distributed widely in animals, plants, and microorganisms. CYP450s can oxidize and degrade many exogenous compounds such as drugs, herbicides, pesticides, some persistent organic pollutants, and so on. Based on recent researches, this paper reviews the nomenclature, classification, structure, and catalytic mechanism of P450 enzymes, and summarizes the research progresses in the metabolism and biodegradation of xenobiotics using P450 enzymes from microorganisms. The nomenclature and classification of the P450 gene superfamily mainly rely on the similarities of amino acid sequences. Although the structures of P450 are conserved, their recognition sites towards to the substrates are variable. This is also the structural basis for the catalytic diversities of P450 enzymes. Few P450 enzymes from bacteria and fungi can metabolize and degrade xenobiotics such as polycyclic aromatic hydrocarbons, herbicides, and so on. However, these P450 enzymes are less likely be used in practical applications because of their low catalytic activities. In the future, more P450 enzymes with high degradable efficiencies towards xenobiotics are needed to be obtained using multiple omics tools or modifying the existing P450 enzymes, to achieve the bioremediation of the environment. © 2018 Science Press. All rights reserved.     

An improved technique for the determination of organic phosphorus in sediments and soils by 31P nuclear magnetic resonance spectroscopy

Knowledge of organic phosphorus (P) species quantity and distribution in sediments and soils is needed to determine the potential for aquatic and terrestrial organism growth. This can be achieved with ³¹P nuclear magnetic resonance spectroscopy (NMR), but resolving peaks within spectra can be problematic because of broadening via paramagnetics, which can cause peaks to overlap. We compared ³¹P NMR spectra of NaOH-EDTA extracts of three sediments and three soils to those that had first been pre-treated with Ca-EDTA-dithionite to remove Fe and Mn, paramagnetics that cause broadening of peaks, but leave organic P alone. Broadening of peaks in Ca-EDTA-dithionite pre-treated samples decreased by 46% and revealed peaks that were hidden compared to untreated samples. The spectrum of one pre-treated soil was similar if not better than the same soil that had received pre-treatment with Chelex resin (also to remove paramagnetics). Therefore, pre-treatment with Ca-EDTA-dithionite is recommended as a simple and cost-effective method for improving organic P idenTIFication and determination in subsequent NaOH-EDTA extracts of sediments and soils rich in Fe and Mn.