Phytotoxic activity of crop residues from Burdock and an active substance

Abstract

Problems related to weed management such as outbreaks of herbicide-resistant weeds have recently increased. An interesting approach to such problems is to use plant materials with phytotoxic activity. Burdock (Arctium lappa L.) is a biennial herb belonging to Asteraceae and is cultivated in several countries. The present study investigated the phytotoxic activity of burdock and its active substances. Extracts of both burdock leaves and roots inhibited the shoot and root growth of cress and barnyard grass, where the level of inhibition increased with increasing extract concentration. The leaf extracts had 2.0–2.5 times higher activity than the root extracts. Bioassay-guided separations of the leaf extracts led to isolation of a phytotoxic substance, onopordopicrin. Onopordopicrin significantly inhibited the shoot and root growth of cress and barnyard grass. The concentrations of the substance required for 50% growth inhibition were 0.27 and 0.26?mM for cress shoots and roots, respectively, and 1.86 and 0.35?mM for barnyard grass shoots and roots, respectively. The present results suggest that burdock leaves have high phytotoxic activity and onopordopicrin may play a major role in the activity. Burdock leaves may be a good resource for weed management.     

陶瓷印花废水处理的混凝剂及工艺条件

采用混凝剂聚合氯化铝（PAC）、聚丙烯酰胺（PAM）、聚合硫酸铁（PFS）对陶瓷印花废水进行混凝沉降处理，监测水样的吸光度、浊度、悬浮物，以脱色率、浊度去除率、悬浮物去除率评价混凝处理的效果。结果表明：PAC是陶瓷印花废水沉降处理的理想混凝剂；水样的吸光度、浊度、悬浮物随混凝剂用量增大和沉降时间延长而呈降低趋势，而脱色率、浊度去除率、悬浮物去除率随混凝剂和沉降时间的增大呈增大的趋势；PAC投加量为20mg／L，沉降时间约为24h，水样脱色率达到90．0％，而当PAC投加量达到100mg／L，沉降时间约为4h，陶瓷印花水的脱色率可达到96．0％。证明了药剂用量的增加与沉降时间的延长对混凝过程具有增效作用。     

聚合物驱采出水中聚丙烯酰胺的微生物联合降解作用研究

通过对2株细菌的培养降解实验研究聚丙烯酰胺(hydrolyzed polyacrylamide,HPAM)降解菌对水环境下聚丙烯酰胺的降解作用,讨论协同降解机理。2株降解聚丙烯酰胺的菌株假单胞菌CJ419、枯草芽孢杆菌FA16在初始30℃废水样品上培养,定期测量细菌生物量和HPAM降解率。培养30 d后CJ419和FA16对聚合物的降解率最大值分别达到30.4%和25%,而以1∶1比例的混合菌降解率最大值达到80.3%。对2株菌胞外各组分研究表明:混合菌降解HPAM的机理主要由胞外降解酶系水解聚合物侧链基团导致HPAM降解为小分子物质,同时生长过程中降解菌还会释放非蛋白还原性物质引发氧化反应共同参与HPAM降解。     

不同质量浓度苦草对铜绿微囊藻生长及抗氧化酶系统的影响

采用苦草（Vallisneria spiralis Linn.）和铜绿微囊藻（Microcystis aeruginosa）共生培养的实验方法,通过追踪测定铜绿微囊藻的生物量、叶绿素a含量、丙二醛（MDA）含量、超氧化物歧化酶（SOD）和过氧化物酶（POD）活性,研究了不同质量浓度苦草对铜绿微囊藻生长及抗氧化酶系统的影响。结果表明,质量浓度大于10 g/L时,苦草对铜绿微囊藻有明显的抑制作用,表现为苦草质量浓度为10、20和40 g/L时,第15天对铜绿微囊藻的抑制率分别为63.3%、94.7%和99.8%,培养过程中,铜绿微囊藻的叶绿素a含量逐渐减少,而SOD、POD活性及MDA含量呈现先增加后逐渐降低的趋势,表明苦草释放的化感物质在经过一定时间积累后能够明显抑制铜绿微囊藻SOD和POD的活性,引起细胞的氧化损伤,促进叶绿素的分解,从而导致藻类死亡,这是苦草抑制铜绿微囊藻生长的原因之一。     

Determination of organochlorine and organophosphate pesticide residues in fruits,vegetables and sediments

Abstract

A method is described for the determination of organochlorine and organophosphate pesticide residues in fruits, vegetables and sediments. The concentrated solvent extract was sealed in a polymeric membrane tube, dialysed in cyclohexane and the solvent replaced with hexane. The organophosphates were analysed on a specific thermionic detector without further clean‐up. For the organochlorine pesticides the extract was eluted through 3 g of alumina and analysed on GC/ECD. The clean‐up for sediment extract was carried out on a10 g alumina column with 100 mL hexane containing 5% acetone and the eluate was concentrated to 5 mL.

The detection limit for organophosphates on a 40 g sample and a final volume of 10 mL was on the average 0.01 mg/kg. The detection limit for organochlorine pesticides, with the final volume of 25 mL, was 0.005 mg/kg for all pesticides except for p,p'‐DDT and endosulfan sulphate, which was 0.01 mg/kg.

The detection limit for oganochlorine pesticides in sediment, with the final volume of 2 mL, was less than 1 μg/kg and for organophosphate pesticides less than 10 μg/kg when the final volume was made to 0.5 mL. At the detection limits the method produced a very high coefficient of variation for both organochlorine and organophosphate pesticides.     

Facilitating substance phase‐out through material information systems and improving environmental impacts in the recycling stage of a product

The amount of electrical and electronic products is increasing rapidly, and this inevitably leads to the generation of large quantities of waste from these goods. Some of the generated e‐waste ends up in regions with sub‐standard recycling systems and may be processed under poor conditions. During uncontrolled incineration, halogenated dioxins and furans can be generated from brominated and chlorinated compounds in the products. In order to reduce the health and environmental risks involved in the recycling stage of the life cycle of electronics, an effective design‐for‐environment process must be established during the product development phase. Knowledge of the chemical substances in the product is crucial to being able to make informed decisions. Through full knowledge of the material content of procured components, phase‐outs of unwanted substances, such as halogenated substances, can be performed in an effective manner. Therefore, information is the key to success in phasing‐out substances; facilitating compliance of legal provisions for manufacturers of electrical and electronic devices; and improving the environmental footprint of products as they reach the end of the life cycle. After an introduction to the challenges of electronics waste management, this paper describes supply chain information systems and how they are used to facilitate substance phase‐outs in the electronics industry. Sony Ericsson has been working with phase‐outs of unwanted substances since it was founded in 2001. Through the introduction of a material declaration system that keeps track of all substances in the components used in the company's products, Sony Ericsson has been able to replace unwanted substances to improve environmental impacts at the recycling stage of a product.     

不同营养水平下悬浮细菌数量对生物粘泥性质的影响

循环水系统中的微生物有悬浮态和附着态,悬浮细菌的存在对附着态生物粘泥的生长及特性有明显影响。通过向模拟循环冷却水系统中投加不同数量初始悬浮细菌,考察在营养水平不同的情况下,悬浮细菌数量对生物粘泥化学组成和脱氢酶活性的影响。结果表明,营养水平不同,初始悬浮细菌数量对生物粘泥的化学组成和脱氢酶活性的影响程度不同;在不同营养水平下,应分别控制初始悬浮细菌数量。贫营养下,初始悬浮细菌数量应控制在6×105个/mL左右;中营养下,初始悬浮细菌数量应控制在1×105～2.6×105个/mL之间;富营养下,初始悬浮细菌数量应控制在0.11×105～2.6×105个/mL之间最不利于生物粘泥的生长。     

SRT对MBR污泥性质的影响

以浸没式膜-生物反应器(SMBR)处理模拟赖氨酸废水为研究体系,考察SRT在10、20和40 d条件下,SMBR中的胞外聚合物(EPS)组分和含量、污泥沉降性能和污泥相对疏水性等污泥性质的变化及其对膜污染的影响。结果表明,随着SRT的延长,混合液中EPS总量呈递减趋势,TBEPS中蛋白质与多糖的比值呈上升趋势,污泥的沉降性能变差,相对疏水性增强;膜通量下降速率变大,膜污染加重。污泥性质与膜污染的相关性表明,膜污染与蛋白质和多糖的比值、污泥沉降性能和相对疏水性呈正相关关系,而与EPS呈负相关关系。     

垃圾渗滤液中有机物分子量的分布及在MBR系统中的变化

利用凝胶层析方法分析了垃圾渗滤液中有机物分子量的分布情况,并考察了利用膜生物反应器(MBR)处理垃圾渗滤液系统中有机污染物分子量的分布以及水溶性腐殖质(AHS)含量的变化．研究发现,垃圾渗滤液中的有机物主要由两部分组成,即分子量大于6000的大分子物质和分子量小于1500的小分子物质．大分子物质主要是水溶性腐殖质,而小分子物质主要由挥发性有机酸及水溶性腐殖质组成．大分子的AHS难以被微生物降解,但能被微滤膜截留．大部分小分子的AHS既难以被微生物降解,又不能被膜截留,是构成MBR处理出水COD的主要成分．     

细胞冻融破碎对城市污泥中重金属浸出浓度的影响

利用反复冻融的方法对污泥细胞进行破碎,考察处理前后污泥重金属的浸出浓度和形态分布的变化,并通过扫描电镜和红外光谱分析污泥中微生物细胞形貌和有机化合物含量的变化.结果显示,经过细胞破碎处理后,污泥中重金属的浸出浓度增大,锌、镍、铬、镉和铜的浸出浓度比原始污泥分别增加了9.7%、5.1%、25%、9%和50%.不稳定态增加,锌和镍的不稳定态分别增加了20.4%和37.9%,锌、镍、铬和铜的有机态分别减少了4.2%、8.2%、1.2%和5.1%.细胞发生了形貌上的变化,细胞体破碎程度严重.细胞EPS以及污泥中的蛋白质、羧酸、多聚糖等有机基团含量明显减少.细胞破碎后污泥浸出浓度增加的主要原因是污泥中有机态的重金属转化成了其他不稳定态的重金属.