山西高原油松种群遗传多样性

用酸性聚丙烯酰胺凝胶电泳（A-PAGE）技术，分析了山西高原9个油松种群在醇溶蛋白水平上的遗传多样性。135份材料共分离出23条带，其中3条为共有带，多态性高达86．95％。全部材料共出现53种带型，9个不同油松种群的带型有差异，同一种群不同个体的带型也有所不同，说明山西高原的油松在遗传上已产生一定程度分化，在醇溶蛋白水平上呈现出遗传多态性。从供试材料的带型计算出油松遗传分化系数为0．1547。即在种群间的变异占总变异的15．47％，种群内变异为84．53％，大部分的遗传变异存在于种群内，但种群间的分化程度在松属树种中也属于较高水平。根据23个多态位点计算遗传相似系数和遗传距离，进行聚类分析，将山西高原9个油松种群聚为3个类群。     

粘虫颗粒体病毒及其增效因子对粘虫核型多角体病毒的增效作用

生物测定的结果表明,粘虫颗粒体病毒ＰｕＧＶ－Ｐｓ及其增效因子对粘虫核型多角体病毒ＰｓＮＰＶ均有明显的增效作用．粘虫颗粒体病毒不仅能提高粘虫感染ＰｓＮＰＶ的死亡率,而且ＮＰＶ、ＧＶ两种病毒混合感染使粘虫幼虫代谢发育受到抑制,表现为生长缓慢、体重减少等．增效因子的增效作用表现在能显著提高粘虫幼虫的死亡率,降低核型多角体病毒的半致死浓度ＬＣ５０,并缩短半致死时间ＬＴ５０．     

滨海滩涂不同围垦年代垦区农作物重金属累积特征及其与氮、磷的关系

为探明滨海滩涂围垦区农作物重金属累积特征及其与围垦年代、作物氮磷含量及化学计量比的关系,采集盐城地区不同围垦年代(围垦20、30、40、60年)农田4种主要作物(大麦、小麦、油菜、蚕豆)样品63个,测定了其根、茎叶和籽粒中Cd、Cu、Zn、Pb、Hg、As及全氮(N)、全磷(P)和粗蛋白(CP)含量,分析了重金属累积特征及与围垦年代、N、P、CP及N/P比的关系,并采用单因子污染指数法和内梅罗综合污染指数法对重金属污染程度和安全水平进行了评价。结果表明,1)围垦农田作物整株各指标含量分别为Cd (0.52±0.94)、Cu (12.98±16.00)、Zn (34.93±27.91)、Pb (3.50±5.88)、Hg (0.0063±0.0063)、As (1.94±3.72) mg·kg~(-1)及N(13.69±8.27)、P (5.98±2.24)、CP (79.55±49.54) g·kg~(-1);籽粒中则分别为(0.0059±0.020)、(1.83±1.48)、(11.13±4.45)、(0.09±0.30)、(0.0023±0.0036)、(0.0021±0.0048) mg·kg~(-1)及(19.21±7.68)、(6.04±1.64)、(111.78±47.81) g·kg~(-1); 2)作物重金属均表现为根茎叶籽粒,N和CP与之相反,表现为根茎叶籽粒,而P则表现为根籽粒茎叶; 3)不同围垦年代之间作物重金属、N、P、CP含量、N/P比及综合污染指数(Pz)均没有显著差异(P0.05); 4)各作物籽粒6种重金属单因子污染指数均值均小于1,除个别样品Pb超标(超标率11%)外,其他重金属均未超标; 5)作物籽粒重金属Pz均值为0.38,表明该地区作物重金属总体处于安全级,但大麦、小麦、油菜籽粒均有样品Pb含量超过警戒线,个别样品甚至达到重度污染水平; 6)作物整株各重金属之间、重金属与P之间均存在显著正相关(P0.01),而重金属与N、CP、N/P存在显著负相关(P0.01),在籽粒中则相关性均不显著(P0.05)。以上结果显示,盐城滨海滩涂围垦区作物重金属累积与围垦时间关系不大,其含量目前尚处于可接受范围内,但Pb污染值得关注,作物重金属与P之间存在一定的相互促进作用,而与N存在一定的拮抗作用,高氮低磷的机体养分状况有助于降低重金属含量。     

α7nAChR在氯化甲基汞神经毒性中的作用

为探讨环境染污染物氯化甲基汞(methylmercury chloride,Me Hg Cl)的神经毒性作用机制,采用MTT、免疫细胞荧光、dot Blot、qRT-PCR等实验技术检测Me Hg Cl对PC12细胞活性及其α7亚型烟碱型胆碱能受体(α7 nicotinic acetylcholine receptor,α7n AChR)蛋白和mRNA表达水平的影响。结果显示Me Hg Cl抑制PC12细胞活性,显著降低α7n AChR的蛋白和mRNA的表达水平,呈浓度依赖性。上述结果表明,Me Hg Cl对神经细胞毒性作用可能与抑制α7n AChR表达有关。     

外源NO介导Cu~(2+)胁迫下番茄幼苗活性氧与内源NO代谢的研究

采用营养液培养方法,研究Cu~(2+)胁迫下外源一氧化氮(nitric oxide,NO)介导的番茄幼苗活性氧及NO代谢途径。结果表明:在Cu~(2+)胁迫下,番茄叶片和根系氧自由基含量增加,NO释放量以及硝酸还原酶(nitrate reductase,NR)和一氧化氮合酶(nitric oxide synthase,NOS)活性降低。外源NO能提高Cu~(2+)胁迫下番茄叶片NR和NOS活性,促进NO的产生,根系NOS活性及NO产量也同时上升。外源NO使精氨酸含量显著增加,而Hb(牛血红蛋白,NO清除剂)可部分抵消NO的促进作用,使Cu~(2+)+SNP+Hb处理下番茄精氨酸含量显著下降。可见,外源NO的加入可通过酶促和非酶促途径促进Cu~(2+)胁迫下NO的合成,介导NO信号调控网络,调节内源NO、精氮酸和活性氧代谢途径,从而缓解过多Cu~(2+)引起的氧化伤害。     

An extraction-assay system: Evaluation on flavonols in plant resistance to Pb and Cd by supercritical extraction-gas chromatography

In this research, supercritical carbon dioxide extraction (SFE) showed better extraction effect when compared with Solid- liquid extraction (SLE), Soxhlet extraction (SE) and Ultrasonic extraction (UE), not only in the rate but also the time. The comparison among these three extraction modifiers, including acetone, ethanol and methanol demonstrated that ethanol was preferred to SFE due to its high extraction effect and low toxicology. In addition, parameter of SFE, influence of temperature and pressure were investigated, and the best extraction effect was achieved at the optima conditions, temperature of 40°C and the pressure of 35 MPa. Thus, SFE is a highly effective method for flavonols extraction, requiring minimum energy and producing non-toxic byproduct. SFE-GC system is applied for the evaluation on flavonols that plays a key role in plant resistance to heavy metal, with its content and synthetase gene expression significantly increasing in plant when threatened by heavy metal. Besides, results indicated that flavonols can improve plant resistance to oxidative stress by quenching the redundant ROS in matrix.

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Enantioselective aquatic toxicity of current chiral pesticides

Chiral pesticides are ubiquitous in the aquatic environment, and their enantioselectivities in aquatic toxicity are known to be complicated. The difference in enantioselective effects between enantiomers may sometimes differ by approximately 100-fold or more, which makes it important to incorporate enantioselective effects into the risk assessment of chiral pesticides. In this paper, we reviewed relevant work on the aquatic toxicity of chiral pesticides with an emphasis on the enantioselective aquatic toxicity under both chronic and acute exposure conditions. We provided a personal account of the importance of studies on molecular mechanisms of developmental toxicity and specific endpoints such as vitellogenin, yolk sac edema and pericardial edema in future research. Given the widespread use of chiral pesticides, we suggest that a more comprehensive understanding of the significance of enantioselective aquatic toxicity will be very helpful in improving risk assessment and regulation of chiral pesticides.     

Characteristics and assessment of phthalate esters in urban dusts in Guangzhou city, China

Phthalate esters (PAEs) were examined in indoor and outdoor dust samples from the subtropical city of Guangzhou, China. The ∑(16)PAEs concentrations ranged from 121 to 3,223 μg g(-1) dust, with the median concentration of 840 μg g(-1) dust. Significantly higher concentrations of PAEs in dust samples were found in offices where electrical and electronic devices, carpet pads, and office furniture were widely used. Of the 16 PAEs, diisobutyl phthalate (DiBP), di-n-butyl phthalate (DnBP), and di(2-ethylhexyl) phthalate (DEHP) dominated the PAEs in indoor and outdoor dust samples, and accounted for >96.8% and >93.1% of the ∑(16)PAEs concentrations, respectively. The median daily inhalation exposure of ∑(16)PAEs were 3.53 and 0.247 μg kg(-1) body weight day(-1), and at the 95(th) percentile were 7.62 and 0.530 μg kg(-1) body weight day(-1), up on the measured concentrations and estimated dust ingestion rates, respectively, for toddles and adults. The ubiquitous distribution of PAEs as noted in this study suggests the need for detailed assessment of PAEs concentrations using more sites and to further investigate the factors influencing PAEs exposure in China.     

三槽式切换氧化沟运行工况数学模式及应用

三槽式切换氧化沟运行工况呈周期性的变化。根据理论分析，建立了各槽活性污泥浓度变化及相互关系的数学模式，并进行了验证。同时就数字模式在周期程序设置及排泥方式选择时的应用做了说明。     

碘量法测定水中溶解氧有关问题的探讨及改进

碘量法测定溶解氧时,采用NH3·H2O—KI代替NaOH(KOH)—KI固定溶解氧,用H2SO4—H3PO(41+1)混合酸代替H2SO4溶解沉淀,使沉淀沉降速度加快,分界线明显,沉淀溶解也更完全。同时做样品空白实验,校正了氧化还原性物质产生的干扰,对废水有明显的抗干扰能力。通过对蒸馏水、自来水、池塘水、废水进行溶解氧测定,结果均非常满意。