Trail discrimination signal of Lasius japonicus (Hymenoptera: Formicidae)

Summary. Trail-following behavior of Lasius japonicus was colony-specific in the field, while trail pheromone activity was not. We found that the footprint substance caused colony-specific trail-following behavior only when working in conjunction with the trail pheromone. The footprint substance alone did not lead the workers to follow trails. The substance consisted mainly of hydrocarbons with composition almost identical to that of cuticular hydrocarbons, except for the absence of n-alkanes. Nestmate workers shared footprint hydrocarbon profiles as well as cuticular hydrocarbons, but the profiles differed among colonies. We therefore consider that the footprint hydrocarbon profiles serve as the trail discrimination signal in L. japonicus.     

根据具体情况优化EPA8310中色谱分离条件

运用Agilent（安捷伦）1200系列高效液相色谱和多环芳烃专用柱ZORBAX Eclipse PAH（4.6×250mm、5μm,P.N.959990-918,S.N.USPAB01066）,对16种多环芳烃化合物混合溶液进行分析,根据具体实验条件优化EPA8310中色谱分离条件并得到了更节省时间、分离效率更好的流动相梯度变化程序。     

4阶导数光谱法同时测定酚类及芳胺的统计性检验

介绍４阶导数光谱法同时测定污水中酚类及芳胺方法的统计性检验，通过样品加标回收实验以及Ｆ检验和ｔ检验证明该方法的精密度和准确度均优于国家环保局推荐的４－氨基安替比林先度法删酚和萘乙二胺偶氮光度法测芳胺的实验方法。     

Electrochemical or UV-photochemical oxidation of industrial wastes containing polar aromatic sulphonates

BACKGROUND AND INTENTION: Aromatic sulphonates other than surfactants and their hydroxy and amino-derivatives are important intermediates for the production of azo dyes. Their production on a large scale can be detrimental for the environment, if the by-products of their synthesis are not disposed of appropriately. An industrial waste, the organic components of which were mainly amino and hydroxy-substituted aromatic sulphonates, seriously endangers the environment close to an dismissed Italian industrial site. Inorganic sulphates and chlorides contained in the waste seriously hinder its disposal by incineration, since they corrode furnace walls. In this work, preliminary exploration of aqueous-phase electrochemically and photochemically induced oxidation techniques have been performed as possible alternatives to incineration. METHODS: Electrochemically-induced oxidation was experimented on individual aromatic sulphonates and on an industrial waste by electrolysing them between smooth platinum electrodes at low temperature (5 degrees C) and high current densities (0.4 A/cm2) with aqueous 0.5 M NaHSO4 electrolyte. Photochemically-induced oxidation was performed by irradiating individual aromatic sulphonates or industrial waste with a 500 W mercury lamp in the presence of sodium peroxydisulphate. RESULTS AND DISCUSSION: After 200 min electrodegradation, 90% of the original compounds disappeared, while 50% Total Organic Carbon (TOC) of an industrial waste was removed from solution after 10 hours. After 180 min UV-photodegradation, 90% of two test aromatic sulphonates disappeared, while 65% of TOC of industrial waste was removed after 5 hours. CONCLUSIONS: Two methods, electrochemical and UV-persulphate oxidation of an industrial waste, were used in order to propose a disposal procedure alternative to incineration. Electrodegradation with smooth Pt anode in 0.5 M NaHSO4 at 5 degrees C halved TOC concentration within 10 hours, while persulphate-assisted UV-photochemical oxidation with a 500 W high pressure Hg lamp abated two-thirds of TOC concentration after 5 hours. Energetic consumption of electrodegradation was 0.33 kWh/g TOC, while that of photooxidation was larger than 2 kWh/g TOC. Although both techniques can be considered efficient from a purely chemical point of view, since both are capable of wet-oxidising the aromatic sulphonates and the industrial waste, electrodegradation seems more promising than a photochemical degradation if economical considerations are also taken into account. Considering also that neither cell design nor catalyst were optimised in this preliminary study, the energy yield of electrodegradation seems likely to be largely improved.     

In situ bioremediation of a hydrocarbon polluted site with cyclodextrin as a coadjuvant to increase bioavailability

Bioavailability is one main factor that influences the extent of biodegradation of hydrocarbons. They are very poorly soluble in water and easily adsorbed to clay or humus fractions, so they pass very slowly to the aqueous phase where they are metabolised by microorganisms. Cyclodextrins are natural compounds that form soluble inclusion complexes with hydrophobic molecules and increase degradation rate of hydrocarbons in vitro. In the perspective of an in situ application, we previously checked that -cyclodextrin does not increase eluviation of hydrocarbons through the soil and consequently does not increase the risk of groundwater pollution. The results of an in situ application of -cyclodextrin for bioremediation of a hydrocarbon polluted site are presented. We stated that the combination of bioaugmentation and enhanced bioavailability due to -cyclodextrin was effective for a full degradation.     

Habitat function of agricultural soils as affected by heavy metals and polycyclic aromatic hydrocarbons contamination

Ecotoxic activity of soils polluted with polycyclic aromatic hydrocarbon (PAH) and heavy metals (HM) was evaluated in pot and laboratory experiments. Plants and soil microorganisms were chosen as test organisms and six different soil materials were used in the study. The applied levels of HM and PAH were aimed to reflect environmental conditions in the "worst case" situation. Zn(2+), Pb(2+) and Cd(2+) were introduced to the soils as an aqueous solution of the mixture of salts at the concentrations corresponding to 1000, 500 and 3 mg kg(-1), respectively. Mixture of four PAH compounds (flourene, anthracene, pyrene and chrysene) as a CH(2)Cl(2) solution was applied at levels of 10-100 mg summation operator 4PAH kg(-1). Population and activity of soil microflora was evaluated as measured of total bacteria counts, intensity of respiration and enzyme activity (dehydrogenases and phosphatases). Effect on plants was evaluated on the base of the growth (plant at an early stage of their development) and yield (mature plant) measurements. The results indicate that combined effect of PAH and heavy metals on soil microorganisms activity and on some plants at an early stage of their development can be stronger than in soils amended with HM or PAH separately. Reaction of tested organisms was related to soil properties, PAH concentration, time and plant species. Mature plants (maize) were insensitive to the applied levels of both group of contaminants.     

大庆地区总悬浮微粒中苯溶物及多环芳烃的测定与评价

通过对大庆地区总悬浮微粒（TSP）中主要化学组成──苯溶物、多环芳烃的测定分析得知：苯溶物占TSP的百分含量，年均值为10．31％，在空气中的平均浓度为12．5μg／m3。与北京燕山地区1983～1984年3个生活区（迎风、东风、东炼）苯溶物年平均值比较，大庆地区苯溶物含量较低。而对总悬浮微粒中多环芳烃的测定结果可明显看出各点采暖期苯并（a）芘、多环芳烃总量的浓度虽都明显高于非采暖期，但其致癌强度和浓度都比北京市、太原市及兰州市弱、低。     

大气TSP采样滤膜上PAHs分布的均匀性研究

标准参考物质是分析法研究的基础，也是质量保证较为可信的手段。本文通过对大气ＴＳＰ采样滤膜上ＰＡＨｓ分布的均匀性研究，发现ＰＡＨｓ在滤膜上是均匀分布的，由此，我们提出了滤膜四等分法和八等分法，以获得可用于分析方法研究的实验用参考物质。     

水体沉积物中有毒有机污染物的监测研究进展

介绍了水体沉积物中有毒有机污染物监测的预处理技术,重点评述了我国水体沉积物中主要有毒有机污染物多环芳烃、多氯联苯和有机氯农药的监测研究现状,认为水体沉积物中有毒有机污染物研究领域今后发展的重点和方向是广泛开展国内主要河流、湖泊、海洋的监测研究和其在水体环境中的迁移及转化机理、生殖毒性以及污染消减与修复技术研究;加强新型预处理技术及其与大型仪器联用技术的研究;尽早建立水体沉积物中有毒有机污染物的监测方法标准及污染评价标准。     

Synthesis, separation and identification of dinitropyrene isomers

Dinitropyrenes (DNP) were prepared by nitration of pyrene, and the product was characterized by MS and elemental analysis. Three isomers of DNP were separated by HPLC and identified by 1H-NMR. The eating sequence on the normal phase column is 1, 3-DNP, 1, 6-DNP and 1, 8-DNP, whereas is 1, 6-DNP, 1. 8-DNP and 1. 3-DNP on the reversed phase column. The separation of three DNP isomers under different chromatographic conditions was also discussed.