Recycling and utilization of metabolic wastes for energy production is an index of biochemical adaptation of fish under environmental pollution stress

The activity levels of lactate dehydrogenase andlactic acid were assessed in various tissues of the fishduring exposure to lethal concentration of group-IIPyrethroids (deltamethrin, cypermethrin, fenvalerate andfluvalinate) for a period of 72 hours. The results showedsteady increased levels in all the tissues (blood,muscle, brain and liver) with response patterncharacteristic of their own. The increased LDH activityand lactic acid levels indicate the shifting of aerobicglycolysis to anaerobiosis and its further utilizationfor energy production during adaptation to toxic stress.     

Spatial Relationships Between Water Quality and Pesticide Application Rates in Agricultural Watersheds

Pesticide applications to agricultural lands in California, USA, are reported to a central data base, while data on water and sediment quality are collected by a number of monitoring programs. Data from both sources are geo-referenced, allowing spatial analysis of relationships between pesticide application rates and the chemical and biological condition of water bodies. This study collected data from 12 watersheds, selected to represent a range of pesticide usage. Water quality parameters were measured during six surveys of stream sites receiving runoff from the selected watershed areas. This study had three objectives: to evaluate the usefulness of pesticide application data in selecting regional monitoring sites, to provide information for generating and testing hypotheses about pesticide fate and effects, and to determine whether in-stream nitrate concentration was a useful surrogate indicator for regional monitoring of toxic substances. Significant correlations were observed between pesticide application rates and in-stream pesticide concentrations (p < 0.05) and toxicity (p < 0.10). In-stream nitrate concentrations were not significantly correlated with either the amount of pesticides applied, in-stream pesticide concentrations, or in-stream toxicity (all p > 0.30). Neither total watershed area nor the area in which pesticide usage was reported correlated significantly with the amount of pesticides applied, in-stream pesticide concentrations, or in-stream toxicity (all p > 0.14). In-stream pesticide concentrations and effects were more closely related to the intensity of pesticide use than to the area under cultivation.     

Simultaneous determination of eight metabolites of organophosphate and pyrethroid pesticides in urine

A simultaneous method for quantifying eight metabolites of organophosphate pesticides and pyrethroid pesticides in urine samples has been established. The analytes were extracted using liquid–liquid extraction coupled with WCX solid phase extraction (SPE) cartridges. Eight metabolites were chemically derivatized before analysis using gas chromatography–tandem mass spectrometry (GC–MS–MS). The separation was performed on a HP-5MS capillary column (30 m × 0.25 mm × 0.25 µm) with temperature programming. The detection was performed under electro-spray ionization (ESI) in multiple reaction monitoring (MRM) mode. An internal standard method was used. The extraction solvent, types of SPE cartridges and eluents were optimized by comparing the sample recoveries under different conditions. The results showed that the calibration curves of the five organophosphorus pesticides metabolites were linear in the range of 0.2–200 μg/L (r² ≥ 0.992) and that of the three pyrethroid pesticides metabolites were linear in the range of 0.025–250 μg/L (r² ≥ 0.991). The limits of detection (LODs, S/N ≥ 3) and the limits of quantification (LOQs, S/N ≥ 10) of the eight metabolites were 0.008–0.833 μg/L and 0.25–2.5 μg/L, respectively. The recoveries of the eight metabolites ranged from 54.08% to 82.49%. This efficient, stable, and cost-effective method is adequate to handle the large number of samples required for surveying the exposure level of organophosphorus and pyrethroid pesticides in the general population.     

4种农药对3种拟菊酯杀虫剂在不同光源下的光解效应

以太阳光、氙灯、高压汞灯为光源,研究了哒嗪硫磷、多菌灵、克百威、丁草胺4种农药对氯氰菊酯、溴氰菊酯、氰戊菊酯3种拟菊酯杀虫剂的光解速度及光解效应的影响。结果表明：哒嗪硫磷、多菌灵对氯氰菊酯等3种拟菊酯杀虫剂在3种不同光源的光照处理下均表现出光敏降解效应;然而在太阳光及高压汞灯光源的光照处理下,克百威和丁草胺对３种拟菊酯杀虫剂具有光猝灭降解作用。太阳光照射下氯氰菊酯等3种拟菊酯杀虫剂的光解率与其单位面积上的药剂剂量成反比;而哒嗪硫磷等4种农药对3种拟菊酯杀虫剂的光敏或光猝灭效率与此4种农药的剂量成正相关     

Effect of copper on the degradation of pesticides cypermethrin and cyhalothrin

The influence of coexisting copper (Cu) ion on the degradation of pesticides pyrethroid cypermethrin and cyhalothrin in soil and photodegradation in water system were studied.Serial concentrations of the pesticides with the addition of copper ion were spiked in the soil and incubated for a regular period of time,the analysis of the extracts from the soil was carried out using gas chromatography (GC).The photodegradation of pyrethroids in water system was conducted under UV irradiation.The effect of Cu~(2 ) on the pesticides degradation was measured with half life (t_(0.5)) of degradation.It was found that a negative correlation between the degradation of the pyrethroid pesticides in soil and Cu addition was observed.But Cu~(2 ) could accelerate photodegradation of the pyrethroids in water.The t_(0.5) for cyhalothrin extended from 6.7 to 6.8 d while for cypermethrin extended from 8.1 to 10.9 d with the presence of copper ion in soil.As for photodegradation,t_(0.5) for cyhalothrin reduced from 173.3 to 115.5 rain and for cypermethrin from 115.5 to 99.0 min.The results suggested that copper influenced the degradation of the pesticides in soil by affecting the activity of microorganisms.However, it had catalyst tendency for photodegradation in water system.The difference for the degradation efficiency of pyrethroid isomers in soil was also observed.Copper could obviously accelerate the degradation of some special isomers.     

Occurrence of Sediment-Bound Pyrethroids in Danish Streams and their Impact on Ecosystem Function

In a total of 189 water samples collected from Danish streams no traces of the pyrethroid esfenvalerate were detected. However, pyrethroids have previously been found in sediments in 9 out of 30 streams investigated. We found that the shredding activity of the Trichopteran Sericostoma personatum and the amphipod Gammarus pulex was significantly reduced with increased concentration of the pyrethroid lambda-cyhalohtrin adsorbed to the leaves on which they fed. Predation rate on the Plecopteran Leuctra nigra by the leech Erpobdella octoculata increased significantly with increasing concentration of lambda-cyhalothrin on the leaves on which L. nigra was fed. Our results clearly indicate that the ongoing monitoring of pesticides is likely to underestimate pyrethroid occurrence and that sediment-bound pyrethroids have a potential negative impact on ecosystem function and biotic interactions in streams.     

Induction of micronuclei in bone marrow cells and hepatotoxicity of one of the most common over-the-counter pyrethroid insecticide products in Nigeria

Increasing environmental pollution in the tropics is creating a breeding ground for mosquitoes, leading to increasingly frequent use of insecticides to combat home infestation of mosquitoes, the vector of malarial parasites. Household members are therefore more prone to aerosol exposure and subsequent health effects. We assessed the hepatotoxic and clastogenic effects in rats exposed to different levels of aerosols of one of the insecticides most commonly in used in Nigeria. There were significant (p?2 in the groups of rats exposed to the aerosols when compared with the control group. In addition, rats exposed to the insecticide aerosols have elevated activities of serum enzymes: γ-glutamyl transferase, aspartate amino transferase and alanine amino transferase, as well as number of micronuclei scored in the bone marrow, at levels that are significantly (p?相似文献   

微生物降解拟除虫菊酯类农药残留的研究进展

随着拟除虫菊酯类农药使用量不断增加,产生的农药残留问题对生态环境和人类健康造成了危害.对降解拟除虫菊酯类农药的微生物种类、降解酶和降解机制及降解酶基因克隆和构建工程菌等方面进行综述,旨在为研究和开发微生物降解拟除虫菊酯类农药残留提供参考.     

Toxicity of the pyrethroid pesticide fenvalerate to freshwater catfish clarias gariepinus: Lethality,biochemical effects and role of dietary ascorbic acid

Static bioassays were made in the laboratory to determine lethal concentration of the pyrethroid pesticide fenvalerate [(RS)-alpha-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate] for the freshwater catfish Clarias gariepinus and effects of sublethal concentrations of the pesticide on some biochemical parameters of the fish. For exposure periods of 24 to 96 h, LC₅₀ values of fenvalerate ranged from 5.83–4.76 μ g/L and 4.24–2.94 μ g/L, respectively for water and acetone soluble fenvalerate. Two sublethal concentrations of fenvalerate were used in the bioassays for biochemical parameters: 2.1 μ g/L for 24 h and 1.4 μ g/L for 96 h exposure, both concentrations representing 50% of LC₅₀ value of acetone soluble fenvalerate for the respective exposure period. Hepatosomatic index, liver glycogen, alkaline phosphatase of liver and ascorbic acid of blood, liver, and kidney decreased while haemoglobin (Hb) %, plasma glucose levels and acid phosphatase level of liver increased after 24 h exposure to 2.1 μ g/L fenvalerate. Longer exposure (96 h) to even a lower concentration (1.4 μ g/L) of fenvalerate resulted in reduction of all the parameters (except Hb %) tested as compared with control. Fish previously fed for 60 days with a diet supplemented by a high level of ascorbic acid (100 mg/100 g diet) could reverse most of the effects caused by 24 h exposure to 2.1 μ g/L fenvalerate. A lower level of ascorbic acid (50 mg/ 100 g diet) supplement could not influence these effects of fenvalerate. Even the higher dose of ascorbic acid supplementation (100 mg/100 g diet) could not relieve the stress parameters, except for Hb% and HSI, when the pesticide was applied at 1.4 μ g/L for a longer time period (96 h).     

超高压液相色谱/质谱联用法测定水中拟除虫菊酯类农药研究

建立了水中6种拟除虫菊酯类农药的超高压液相色谱/质谱联用分析方法.对液相色谱和质谱两方面条件进行优化,采用多反应监测（MRM）模式分析,各组分在0.005～0.1 mg/L范围内线性关系良好,相关系数（R）均大于0.998;6种拟除虫菊酯类农药的最低检出限为0.000 5 ～0.002 mg/L,其中,溴氰菊酯的方法检出限满足《地表水环境质量标准》限值要求;各组分的加标回收率在92.8％～103％;相对标准偏差（RSD）均小于5％（n=6）.该方法简单、快捷,可用于实际水样的直接测定.