再生水对作物种子萌发、幼苗生长及抗氧化系统的影响

以小麦、黄瓜、西红柿为供试材料,研究再生水水培对小麦、黄瓜和西红柿种子萌发、生长发育及其活性氧清除系统的影响.结果表明,再生水对小麦种子发芽率有明显的促进作用,对西红柿种子无显著影响,而黄瓜种子表现出一定的抑制作用;对各物种幼苗生长发育有一定促进作用,再生水灌溉对小麦、黄瓜及西红柿叶片活性氧清除系统均无不利影响;作物各叶绿素及蛋白质含量也显著高于对照.研究结果表明,再生水可以替代自来水进行作物灌溉,但灌溉过程中需采取适当的措施,使再生水利用效果最佳.     

PPCPs在不同营养级水生生物体内的累积与代谢

在总结药品及个人护理品(PPCPs)在水环境中分布特征的基础上,分析和对比了典型PPCPs在不同营养级水生生物(浮游植物、底栖生物和鱼类)体内的累积规律,并阐述了PPCPs在鱼体内的代谢转化途径和机理.提出未来该领域的主要研究方向包括加强对个人护理品生物累积和食物链传递的研究,深入探索PPCPs在食物链上的传递和累积规律,开展实际水体中PPCPs的代谢转化研究.     

硫化物胁迫对日本沼虾呼吸代谢和能量代谢酶的影响

研究了硫化物暴露后日本沼虾细胞色素氧化酶(CCO)、琥珀酸脱氢酶(SDH)、延胡索酸还原酶(FRD)和乳酸脱氢酶(LDH)4种呼吸代谢酶及能量代谢酶-精氨酸激酶(AK)活性的变化规律.将日本沼虾暴露于0.6 mg·L~(-1)、2mg·L~(-1)的2个硫化物质量浓度组和不含硫化物的对照组水体中,暴露后0、2、12、24、48 h和解除暴露后48 h取肝胰腺和肌肉组织进行酶活性分析.结果显示:肝胰腺和肌肉组织SDH和CCO活性随硫化物质量浓度升高或暴露时间延长而显著降低(P<0.05).FRD、LDH和AK活性随硫化物质量浓度升高或暴露时间延长而显著升高(P<0.05).解除硫化物暴露后48 h,各质量浓度组酶活性与对照组无显著差异.上述酶活性还存在组织差异,肝胰腺呼吸代谢酶活性高于肌肉中相应酶活性,而AK活性与此相反.结果表明,硫化物胁迫导致日本沼虾有氧呼吸代谢减弱,无氧呼吸代谢增强,并动用其能量贮存物质磷酸精氨酸,产生更多ATP以适应外界不良环境.     

同位素示踪法检测废水中TCC／TCS生物毒性的研究

用同位素示踪法测定微生物的葡萄糖摄入量,可能检测废水中有毒物质的生物毒性。实验结果显示：ＴＣＣ／ＴＣＳ对废水处理系统中厌氧菌的葡萄糖摄入有抑制作用,其抑制率与接触剂量的对数呈线性关系,但与接触时间却没有明显的线性关系。由此可见,ＴＣＣ／ＴＣＳ对微生物葡萄糖摄入的影响是复杂的。当生物处理系统中的微生物未接触ＴＣＣ／ＴＣＳ时,１０％有作用浓度（ＥＣ１０）和５０％有作用浓度（ＥＣ５０）分别为１．７１ｍｇ     

Detoxification and repair process of ozone injury: from O3 uptake to gene expression adjustment

Plants react to O₃ threat by setting up a variety of defensive strategies involving the co-ordinated modulation of stress perception, signalling and metabolic responses. Although stomata largely controls O₃ uptake, differences in O₃ tolerance cannot always be ascribed to changes in stomatal conductance but cell protective and repair processes should be taken into account. O₃-driven ROS production in the apoplast induces a secondary, active, self-propagating generation of ROS, whose levels must be finely tuned, by many enzymatic and non-enzymatic antioxidant systems, to induce gene activation without determining uncontrolled cell death. Additional signalling molecules, as ethylene, jasmonic and salicylic acid are also crucial to determine the spreading and the containment of leaf lesions. The main recent results obtained on O₃ sensing, signal transduction, ROS formation and detoxification mechanisms are here discussed.     

Pteris vittata – Revisited: Uptake of As and its speciation, impact of P, role of phytochelatins and S

Pteris vittata is known to hyperaccumulate As but the mechanism is poorly understood. We found an increase of As concentration with increasing soil solution As concentrations, but P application had no impact, although plant P concentrations responded to different rates of P supply. As in fronds was dominantly (82–89%) present in the form of AsIII. In roots we detected 45% as AsIII which is higher than reported in previous studies and supports substantial As-reduction to take place in roots. We detected PC2/3GS–AsIII, PC2–GS–AsIII and (PC2)2–AsIII in increasing amounts with application of As. The total amount of PC was in the range reported previously and far too small to assign a significant role in As detoxification to PCs. The close correlation between S and As in fronds and the lack of data on sulphur uptake and metabolism indicates the need for a detailed investigation on sulphur nutritional status and As metabolism in P. vittata.     

Metabolism of nC11 fatty acid fed to Trichoderma koningii and Penicillium janthinellum II: Production of intracellular and extracellular lipids

Abstract

Little is known about the fungal metabolism of nC₁₀ and nC₁₁ fatty acids and their conversion into lipids. A mixed batch culture of soil fungi, T. koningii and P. janthinellum, was grown on undecanoic acid (UDA), a mixture of UDA and potato dextrose broth (UDA+PDB), and PDB alone to examine their metabolic conversion during growth. We quantified seven intracellular and extracellular lipid classes using Iatroscan thin-layer chromatography with flame ionization detection (TLC-FID). Gas chromatography with flame ionization detection (GC-FID) was used to quantify 42 individual fatty acids. Per 150 mL culture, the mixed fungal culture grown on UDA+PDB produced the highest amount of intracellular (531 mg) and extracellular (14.7 mg) lipids during the exponential phase. The content of total intracellular lipids represented 25% of the total biomass-carbon, or 10% of the total biomass dry weight produced. Fatty acids made up the largest class of intracellular lipids (457 mg/150 mL culture) and they were synthesized at a rate of 2.4 mg/h during the exponential phase, and decomposed at a rate of 1.8 mg/h during the stationary phase, when UDA+PDB was the carbon source. Palmitic acid (C_16:0), stearic acid (C_18:0), oleic acid (C_18:1), linoleic acid (C_18:2) and vaccenic acid (C_18:1) accounted for >80% of the total intracellular fatty acids. During exponential growth on UDA+PDB, hydrocarbons were the largest pool of all extracellular lipids (6.5 mg), and intracellularly they were synthesized at a rate of 64 μg/h. The mixed fungal species culture of T. koningii and P. janthinellum produced many lipids for potential use as industrial feedstocks or bioproducts in biorefineries.     

Metabolism of gamma‐hexachlorocyclohexah (HCH) in vivo. Metabolism of orally administered gamma‐2,3,4,5,6‐pentachlorocyclohexen (PCCH)

Abstract

Mexacarbate (4‐dimethylamino‐3,5‐xylyl N‐methylcarbamate) insecticide has potential for use in spruce budworm (Choristoneura fumiferana Clem.) control operations in Canada. Its persistence and fate in balsam fir (Abies balsamea (L.) Mill.), litter and soil samples were studied by spraying aerially oil‐based and water‐based formulations, each at 70 g A.I./ha over a coniferous forest near Bathurst, New Brunswick. The oil‐based formulation gave the maximum concentration of the chemical in the substrates studied. In fir needles, the highest concentrations observed were 0.51 ppm and 0.19 ppm (fresh weight) for the oil‐based and emulsion formulations respectively, 1 h after application. The residue levels decreased very rapidly with a half‐life of approximately 5 h. Three and eight days after the spray application of the emulsion and oil formulations respectively, the concentrations of mexacarbate in foliage decreased to trace levels ( 0.008 ppm). Only very low levels of residue were detected in litter and soil. The peak concentrations for the two formulations ranged from 0.02 to 0.11 ppm (fresh weight) in litter and from 0.01 to 0.06 ppm (fresh weight) in soil. The residue levels in both litter and soil decreased to below the detection limit (0.005 ppm) within 1 d. The ground deposit levels found on glass plates and the droplet density and size spectra measured on Kromekote® cards reflected the variations in concentrations found in fir needles, litter and soil samples and correlated with the observed maximum concentrations in them. Under the stipulated use pattern, mexacarbate concentrations found in the terrestrial components studied were low and are not likely to have any undue adverse effects on non‐target species.