不同基质体系中白腐茵对喹啉和吲哚的降解

用单基质及混合基质体系,探讨了白腐菌Pleurotus ostreatus BP对氮杂环化合物的降解规律.结果表明,在弱酸性环境下,白腐菌能有效降解喹啉和吲哚.单摹质体系中,喹啉的降解率15 d内能达到89.48%,98.17%的吲哚6 d内被降解;混合基质体系中,基质(喹啉、吡啶、苯酚及氨氮)的加入能促进白腐菌对吲哚的降解,但(吲哚、吡啶、苯酚及氨氮)却抑制了白腐菌对喹啉的降解.不同基质体系中,白腐菌对喹啉和吲哚的降解分别遵循零级和一级反应动力学.相对单基质而言,混合基质的存在对白腐菌生物学特性产生明显影响,可缩短生长周期,提高生长速率和漆酶活性.漆酶在吲哚的降解中起着重要的作用,但不能完全决定喹啉的降解.     

稻草秆粉基质中白腐茵对三苯甲烷类染料的降解特性

研究了稻草秆粉基质中自腐菌对三苯甲烷类染料（孔雀绿、溴酚蓝和结晶紫）的降解特性．结果表明，白腐菌10d内对三苯甲烷类染料脱色率均可达到93％以上．染料加入对木素过氧化物酶分泌有抑制作用．随着培养过程的进行，染料脱色率增加，脱色降解以漆酶为主．紫外扫描发现，染料吸收波长有偏移，标志着染料结构发生变化，其中溴酚蓝能被完全矿化．图2表2参10     

稻草秆粉基质中白腐菌对三苯甲烷类染料的降解特性

研究了稻草秆粉基质中白腐菌对三苯甲烷类染料(孔雀绿、溴酚蓝和结晶紫)的降解特性.结果表明,白腐菌10 d内对三苯甲烷类染料脱色率均可达到93%以上.染料加入对木素过氧化物酶分泌有抑制作用.随着培养过程的进行,染料脱色率增加,脱色降解以漆酶为主.紫外扫描发现,染料吸收波长有偏移,标志着染料结构发生变化,其中溴酚蓝能被完全矿化.图2表2参10     

白腐菌Trametes hirsute对六氯苯的降解及其条件优化

在液体体系下,筛选了5株白腐菌,对六氯苯进行了降解研究,并优化了白腐菌Trametes hirsute TH对六氯苯的降解条件.结果表明,不同白腐菌均能降解六氯苯,其中白腐菌Trametes sp.TR对六氯苯降解率最高,达90.21%;而白腐菌T.hirsute TH对六氯苯降解率为87.08%,但生物量最高,达3.33 g/L.通过响应面法优化白腐菌T.hirsute TH降解六氯苯的条件,结果显示,转速、接种量和培养时间是影响六氯苯降解的主要因素.优化后的最佳条件为:转速125 r/min,菌丝接种量8%(V/V),培养时间2 d,温度28 ℃,pH为7.在优化条件下,2 d内白腐菌T.hirsute TH对浓度为10 mg/L的六氯苯降解率和降解量分别可达91.52%和2.288 mg L-1 d-1.图2表7参17     

睾丸酮丛毛单胞菌对喹啉类化合物的降解

对喹啉、异喹啉、2-甲基喹啉、3-甲基喹啉、4-甲基喹啉和6-甲基喹啉在睾丸酮丝毛单胞菌(Comamonas testosteroni Q10)作用下的降解及底物之间的相互作用进行研究．结果表明,喹啉和3-甲基喹啉不仅能有效地被降解,而且细菌也有明显的生长,而其它化合物虽有部分降解但没有观察到细胞生长．底物初始浓度的增加对菌Q10有一定抑制作用．喹啉的存在对其它化合物的降解具有不同的促进效应,其中尤以6-甲基喹啉和4-甲基喹啉最为明显．能在较短时间内得到完全去除,而在各二元体系中喹啉的降解受到这些化合物的抑制作用．     

UV-Fenton法促进白腐菌处理草浆造纸蒸煮黑液

UV—Fenton法能够产生羟基自由基氧化草浆造纸蒸煮黑液中的有机质，白腐菌能够降解草浆造纸蒸煮黑液中的木质素，降低黑液COD，但是分别采用两种方法处理草浆造纸蒸煮黑液，效果都不明显．本研究初步探索了UV—Fenton法作为预处理对白腐菌处理草浆造纸蒸煮黑液体系的影响．与仅采用白腐菌处理黑液的效应相比，UV—Fenton法氧化黑液体系中易氧化的物质，改变了体系中难降解物的特性，降低了可溶性糖的含量，结果能提高白腐菌木质素降解酶系的分泌及酶的活性，增强白腐菌降解木质素及去除黑液COD的能力．图5表1参10     

煤气化废水中有机物对磷酸铵镁结晶法去除氨氮的影响

研究了杂环类(吡啶、喹啉)和酚类(间甲酚、二甲酚、苯酚)有机物对磷酸铵镁结晶法(MAP,magnesium ammonium phosphate)处理废水中氨氮的影响.研究表明,杂环和酚类有机物均对MAP法的除氮效果产生抑制作用,杂环类有机物的抑制作用大于酚类有机物,其中加入吡啶、喹啉、间甲酚、二甲酚、苯酚相比于对照组(21 mg·L-1),氨氮残余浓度分别升高45.17、56.66、43.01、50.68、49.72 mg·L-1.因为络合作用和吸附作用,多组分体系MAP晶体产生的抑制作用强于单一组分体系.     

红球菌Chr-9降解吡啶和苯酚的特性

研究了红球菌(Rhodococcus)Chr-9菌株在基础盐培养基中降解吡啶和苯酚的特性,分析了菌株降解苯酚和吡啶间的差异.结果表明,菌株Chr-9能够在72 h内将基础盐培养基中的吡啶(200 mg L-1)和苯酚(200 mg L-1)完全降解,同时利用吡啶和苯酚进行生长.菌株降解吡啶的最适温度为35℃,最适pH为8.0.菌株降解吡啶和苯酚的速度与底物的初始浓度呈负相关;在无其它氮源的基础盐培养基中,菌株能够利用吡啶和苯酚协同生长.图7参12     

自然水体介质中白腐菌对二噁英类物质的降解

研究了自然水体介质中白腐菌射脉侧菌（Phlebia radiata）Ⅰ-5-6对二噁英类物质2，7-二氯二苯并噁英（2，7-diCDD）和八氯二苯并呋喃（OCDF）的降解规律．结果显示，在自然河水为介质的培养环境中，2，7-diCDD随着江水加入量的递增，降解率逐步下降，但这种影响随着培养时间的延长而逐步减弱．白腐菌处理OCDF底物的效果并不理想，经过12d处理后，降解率最高只达到36．00％，这很可能是由于OCDF已经高度氧化，再要对它进行氧化降解比较困难．     

富N条件下白腐菌对联苯的降解

探讨了在富Ｎ条件下白腐菌降解芳香化合物酶的活性变化和对联苯的降解．研究结果表明,ｍ（Ｃ）／ｍ（Ｎ）比值对白腐菌的ＬｉＰ和ＭｎＰ活性有明显的影响;黎芦醇提高了ＬｉＰ和ＭｎＰ的活性及培养基中·ＯＨ基数量,白腐菌在富Ｎ条件下能降解黎芦醇和联苯     

土壤B[a]P叠加污染对蚯蚓体腔细胞SOD、POD和MDA的毒性效应

采用累积试验方法,研究土壤苯并[a]芘（B[a]P）多次叠加污染对赤子爱胜蚓（Eisenia foetida）体腔细胞超氧化物歧化酶（SOD）、过氧化物酶（POD）和丙二醛（MDA）的毒性效应.结果表明,随着土壤中B[a]P暴露时间的延长,蚯蚓体腔细胞的SOD、POD活力和MDA含量呈初期（1～14 d）下降速率较快,尔后（14～56 d）下降速率减小的变化趋势.在叠加污染条件下,0～ 20 cm深度土壤中蚯蚓体腔细胞SOD活力和MDA含量在14d时分别比一次污染低20.97％和15.96％,POD活力比一次污染高20.44％;而在＞20～40 cm深度土壤中蚯蚓体腔细胞SOD、POD活力和MDA含量在14d时分别比一次污染低52.89％、18.00％和70.60％.表明B[a]P叠加污染土壤中蚯蚓体腔细胞的毒性效应低于一次污染.     

Promotive effect of pyridine on indole degradation by activated sludge under anoxic conditions

Batch experiments were carried out to investigate the promotive effect of pyridine on indole degradation under denitrifying conditions. The seed sludge was obtained from a local coal-coking wastewater treatment facility and was acclimated in the laboratory. Indole and pyridine were supplemented to the synthetic wastewater at different ratios. The optimum ratio of chemical oxygen demand (COD) to nitrate (C/N) was 8.4–8.9 for both denitrification and indole and pyridine degradation. At a temperature of 28°C and pH of 7.0–7.5, the nitrate reductase activity (NRA) was in the best state. The addition of pyridine could promote NRA and the degradation of indole. When the initial concentration of indole was 150 mg/L, the concentration ratio of indole to pyridine was in the range of 1–10. Under optimum C/N conditions, the degradation of indole could be described with pseudo-zero-order kinetics. There was no accumulation of nitrite during the reaction. When the concentration ratio of pyridine to indole was less than 0.25 with an increase in the pyridine proportion, there were more significant augment rates for NRA and the degradation of indole than the situation when the concentration ratio was more than 0.25.     

Coupled aerobic and anoxic biodegradation for quinoline and nitrogen removals

Quinoline (C₉H₇N) commonly occurs in wastewaters from the chemical, pharmaceutical, and dyeing industries. As quinoline is biodegraded, nitrogen is released as ammonium. Total-N removal requires that the ammonium-N be nitrified and then denitrified. The objective of this study was to couple quinoline biodegradation with total-N removal. In a proof-of-concept step, activated sludge was sequenced from aerobic to anoxic stages. The ammonium nitrogen released from quinoline biodegradation in the aerobic stage was nitrified to nitrate in parallel. Anoxic biodegradation of the aerobic effluent then brought about nitrogen and COD removals through denitrification. Then, simultaneous quinoline biodegradation and total-N removal were demonstrated in a novel airlift internal loop biofilm reactor (AILBR) having aerobic and anoxic zones. Experimental results showed that the AILBR could achieve complete removal of quinoline, 91% COD removal, and 85% total-N removal when glucose added as a supplemental electron donor once nitrate was formed.     

Dealing with double trouble: consequences of single and double herbivory in Brassica juncea

In their natural environment, plants are often attacked simultaneously by many insect species. The specificity of induced plant responses that is reported after single herbivore attacks may be compromised under double herbivory and this may influence later arriving herbivores. The present study focuses on the dynamics of induced plant responses induced by single and double herbivory, and their effects on successive herbivores. Morphological (leaf length, area and trichome density) and chemical changes (leaf alkenyl and indole glucosinolates) in Brassica juncea were evaluated 4, 10, 14 and 20 days after damage by the specialist Plutella xylostella alone, or together with the generalist Spodoptera litura. To assess the biological effect of the plant’s responses, the preference and performance of both herbivores on previously induced plants were measured. We found that alkenyl glucosinolates were induced 20 days after damage by P. xylostella alone, whereas their levels were elevated as early as 4 days after double herbivory. Trichome density was increased in both treatments, but was higher after double herbivory. Interestingly, there was an overall decrease in indole glucosinolates and an increase in leaf size due to damage by P. xylostella, which was not observed during double damage. S. litura preferred and performed better on undamaged plants, whereas P. xylostella preferred damaged plants and performed better on plants damaged 14 and 10 days after single and double herbivory, respectively. Our results suggest that temporal studies involving single versus multiple attacker situations are necessary to comprehend the role of induced plant responses in plant–herbivore interactions.     

甲草胺热裂解气相色谱-质谱分析

甲草胺是一种广泛用于农作物上的酰胺类除草剂.本文利用裂解气相色谱与质谱联用(Py-GC-MS)研究了甲草胺在热裂解温度200℃、400℃、600℃、800℃下的降解产物和热降解机理.实验结果表明,共有60种裂解产物被分离鉴定,随着温度的升高甲草胺显著分解,当裂解温度超过600℃时,大量的芳烃类、喹啉类、吲哚类化合物在高温裂解中产生,温度越高他们的相对含量也越高.基于对裂解产物的定性和它们含量的变化提出了甲草胺的热降解机理.     

Leaf surface compound fromBrassica oleracea (Cruciferae) induces oviposition byPieris brassicae (Lepidoptera: Pieridae)

Summary Chemicals present on the surface of cabbage (Brassica oleracea L.) leaves were extracted by dipping these leaves for 3 s in dichloromethane followed by a 3 s dip in methanol. When offered in dual choice bioassays using green paper cards as a substrate, the methanol extract stimulated oviposition activity byPieris brassicae L. (Lepidoptera: Pieridae) females. The oviposition stimulant was isolated using medium pressure liquid chromatography, reversed-phase HPLC, ion-pair HPLC and ion exchange chromatography. Using¹H-NMR spectroscopy, the stimulant could be identified as glucobrassicin (3-indolyl-methyl-glucosinolate). When pure glucobrassicin was offered at a dose identical to that in the crude methanol extract, butterflies did not discriminate between these two substrates in a dual choice test. It is argued that a high sensitivity for indole glucosinolates as host recognition factors may confer an adaptive value for these specialist crucifer feeders. The nutritional significance of their precursor tryptophan and the non-volatile nature of the aglycones formed upon enzymic hydrolysis in damaged tissues are proposed as properties of indole glucosinolates that contribute to this possible adaptive advantage.     

焦化废水中溶解性有机物组分的特征分析

焦化废水是典型的具有复杂有机质的工业废水,其复杂的有机构成制约了水处理的水质达标,且可能对排入水体构成危害.为了探明其溶解性有机物的组成,采用XAD-8大孔树脂将焦化废水中的溶解性有机物分为亲水性组分(HIS)、疏水酸性组分(HOA)、疏水碱性组分(HOB)和疏水中性组分(HON),分析了各组分的溶解性有机物(DOC)、紫外-可见光谱、色度,并采用GC/MS对各组分中有机物进行定性分析.结果表明,焦化废水中的有机物主要为HIS和HOA组分,其DOC含量分别占总DOC的44.3%和32.4%;焦化废水在200—250 nm和300—400 nm范围内有特征吸收峰,且吸收光强度顺序为HIS>HOA>HON>HOB;焦化废水的色度主要由HOA和HON构成,其在525 nm和436 nm处的吸光度分别占焦化废水吸光度的42.9%(HON)、42.1%(HON)和21.4%(HOA)、15.8%(HOA);焦化废水中亲水性物质主要是苯胺、苯酚、喹啉、异喹啉,疏水酸性物质中主要是各种甲基取代的酚类物质,疏水碱性物质主要是各种胺类和含氮杂环化合物,疏水中性物质主要是吲哚及其衍生物.     

Enhanced electrokinetic remediation of quinoline-contaminated soils

ABSTRACT

The aim of this investigation was to examine the ability of enhanced electrokinetic (EK) remediation to efficiently remove quinoline from contaminated kaolinite soils. In order to accomplish this, the effect of a voltage gradient and anode buffer concentration on migration of quinoline in kaolinite was determined. The results showed that EK transport process effectively stimulated desorption and movement of quinoline in kaolinite. The rate and distance of migration rose with increasing voltage gradient and anode buffer concentration under certain conditions. The mechanisms that drive quinoline migration by electrodynamic processes were established as attributed to either electromigration or electroosmosis, and both played key roles in driving quinoline to migrate towards the cathode.     

Growth, yield and photosynthesis of Panicum maximum and Stylosanthes hamata under elevated CO2

Plant height, biomass production, assimilatory functions and chlorophyll accumulation of Panicum maximum and Stylosanthes hamata in intercropping systems was influenced significantly under elevated CO2 (600 +/- 50 ppm) in open top chambers (OTCs). The plant height increased by 32.0 and 49.0% over the control in P. maximum and S. hamata respectively in intercropping system under elevated CO2 over open field grown crops (Ca). P. maximum and S. hamata produced 67 and 85% higher fresh and dry biomass respectively under elevated CO2. Rates of photosynthesis and stomatal conductance increased in both the crop species in intercropping systems under elevated CO2. The canopy photosynthesis (photosynthesis x leaf area index) of these crop species increased significantly under elevated CO2 over the open grown crops. The chlorophyll a and b accumulation were also higher in the leaves of both the crop species as grown in OTC with elevated CO2. The increased chlorophyll content, leaf area index and canopy photosynthesis led to higher growth and biomass production in these crop species under elevated CO2. The total carbon sequestration in crop biomass and soils during the three years was 21.53 Mg C/ha under elevated CO2. The data revealed that P. maximum and S. hamata intercropping system is the potential as a sink for the increasing level of CO2 in the atmosphere in the semi-arid tropics.