234 resultados para 205-1255A
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1999年6月至2000年5月对武汉东湖铜锈环棱螺的种群生态学进行了周年研究.铜锈环棱螺年均密度和生物量分别为92.2ind./m2和142.83g/m2,密度和生物量的高峰分别出现在6月(157ind./m2)和11月(205.78g/m2);东湖铜锈环棱螺为一年一代,其一年中种群含有5个年龄组,其中1998年龄组占绝对优势.利用瞬时增长率法计算东湖铜锈环棱螺的周年生产量带壳湿重为91.56g/m2,去壳干重为5.32g/m2,P/B系数为0.64.同时研究了铜锈环棱螺的生产力动态变化,其生产量累积多数
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从野外采回的钉螺在室内各实验温度条件下均能正常产卵,其产卵量的高低与室温无关;在15-30℃的温度范围内,随着温度的升高钉螺的孵化期逐渐缩短;利用有效积温公式得知钉螺卵孵化的有效积温为193.55日度,发育起点温度为10.86℃;在各温度下初孵幼螺随着生长发育,螺壳的长宽比也随之加大.
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本研究对中药甘草(Glycyrrhiza uralensis Fiseh)进行了粗提,将粗提物按0.5%和2%的质量分数制成药饵投喂鲫鱼(Carassius auratus)后,于第14天、28天、35天、42天5、6天采样检测其免疫指标。结果显示,低剂量组试验鱼血清溶菌酶活性逐渐升高,高剂量组在35d达到最大值(205.5±28.8)U/mL,之后略有下降。低剂量组和高剂量组试验鱼血清杀菌活性均有所波动,波动范围分别为62.0%—73.1%和75.0%—83.3%,就各期而言,对照组、低剂量组和高剂量组
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运用随机扩增多态性DNA(RAPD)方法对雌核发育和人工转性鲢、鳙进行了遗传多样性的研究,并用长江天然鲢、鳙群体作为对照分析.在雌核发育鲢中,共得到187条带,其中19条为多态带,占10.16%,而对照组鲢共扩增205条带,有32个多态座位,占总带数的15.61%.在雌核发育鳙中共产生232条带,其中11条为多态带,比例为4.74%,而在对照组中共产生241条带,25条为多态带,比例为10.37%.遗传距离分析表明,雌核发育鲢和鳙的平均值分别为0.102和0.023.而对照组鲢和鳙遗传距离平均值分别为0.
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从滇池蓝藻水华中分离得到的铜锈微囊藻群体在实验室无机营养中解聚成单细胞 ,结果表明 ,群体微囊藻的生长速度明显低于单细胞微囊藻 ;前者具明显可见的胞外酸性多糖胶鞘 ,而单细胞则几乎没有 ;按常规方法分析比较两种细胞形态的毒性大小和毒素组成 ,发现群体微囊藻主要含有三种微囊藻毒素的异构体 ,而单细胞以MC LR为主 ;且单细胞微囊藻的毒性约为群体的 1 0倍。二者的LDH和PGM同工酶酶谱也有差异。本研究为解释毒素的合成和调控机理提供了新的证据
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在渗透系统中 ,念珠藻葛仙米因轻微失水而叶绿素的Fv/Fm 上升 ;水势继续降低时Fv/Fm快速下降。衬质系统和自然失水的影响相似 ,藻体在失去总水分的 94 %以后Fv/Fm 开始下降 ,此前水分的丢失对Fv/Fm 比值的上升稍有促进作用。干燥藻体吸水后Fv/Fm 的恢复速率随着贮藏时间的延长而下降 ,并且Fv/Fm 的恢复对光和蛋白质的重新合成有依赖性。DCMU虽然也抑制Fv/Fm 的恢复 ,但可逆转
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本研究于1989-1990对武汉东湖营养水平不同的二个湖区的颗粒悬浮物的干物质结构和元素组成进行了分析.综合平均值表明,浮游动物的现存量约为浮游植物的1/4,浮游动物群落以小型的原生动物和轮虫占优势.从年平均值来看,浮游生物的干重占颗粒悬浮物干物质的2.5—7.6%,浮游生物碳量占颗粒悬浮物碳量的4.0—9.8%;颗粒悬浮物的碳/氮比与一般浮游植物的比值相似,但明显大于多数浮游动物;颗粒悬浮物的碳与干物重之比约为一般浮游生物的3/4;颗粒悬浮物的灰分含量约为45%,显著高于除硅藻以外的其它浮游生物。从数量
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本文记述了在我国新发现的鳗鲡爱德华氏病的症状和病原菌的特征。病鱼的症状表现为两大类型,以肾脏病变为主的肾脏型和以肝脏病变为主的肝脏型。从病鱼的内脏分离到7株菌,用其中的E86~205进行人工感染,100%的鳗鲡死亡,与自然发病的症状相似,从感染的鳗鲡上又重新分离到菌株E86-203。E86-203与E86-205以及其他菌株的特征也都一致。均为革兰氏阴性杆菌。菌体直,两端圆形,单个,大小为0.6—0.8×0.8—2.4微米。周鞭毛,运动,兼性厌氧,发酵葡萄糖产酸产气。氧化酶阴性,过氧化氢酶阳性,产生硫化氢
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The antialgal activities of benzoic acid, 2-hydroxybenzoic acid (salicylic acid), 3-hydroxybenzoic acid, 4-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid and 3,4,5-trihydroxybenzoic acid (gallic acid) were studied on the growth of two strains of Microcystis aeruginosa (toxic FACHB 942 and non-toxic 469). The results showed that the sequence of 50% growth inhibition concentration (ErC50) of 6- compounds for both strains of M. aeruginosa followed the same order: gallic acid > 3,5-dihydroxybenzoic acid > 4-hydroxybenzoic acid > salicylic acid > 3-hydroxybenzoic acid > benzoic acid. The position and the numbers of hydroxy groups between the hydroxy group and carboxyl influenced the antialgal effects of phenolic acids. We also investigated the joint effects of benzoic acid, 4-hydroxybenzoic acid and 3,4,5-trihydroxybenzoic acid on the growth of M. aeruginosa ( toxic FACHB 942). The mixture of phenolic allelochemicals showed the synergistic effects.
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To investigate the occupational exposure levels to polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polybrominated diphenyl ethers (PBDEs), and polychlorinated biphenyls (PCBs), indoor dust (n = 3) in workshops and hair samples from male workers (n = 64) were collected at two electrical and electronic equipment waste (E-waste) dismantling factories located in the LQ area in east China in July 11-13, 2006. Pre- and postworkshift urines (64 of each) were also collected from the workers to study oxidative damage to DNA using 8-hydroxy-2'-deoxyguanosine (8-OHdG) as a biomarker. The concentrations of PCDD/Fs, PCDD/F-WHO-TEQs, PBDEs, PCBs and PCB-WHO-TEQs were (50.0 +/- 8.1) x 10(3), 724.1 +/- 249.6, (27.5 +/- 5.8) x 10(6), (1.6 +/- 0.4) x 10(9), (26.2 +/- 3.0) x 10(3) pg/g dry weight (dw) in dust, and (2.6 +/- 0.6) x 10(3), 42.4 +/- 9.3, (870.8 +/- 205.4) x 10(3), (1.6 +/- 0.2) x 10(6), 41.5 +/- 5.5 pg/g dw in hair, respectively. The homologue and congener profiles in the samples demonstrated that high concentrations of PCDD/Fs, PBDEs, and PCBs were originated from open burning of E-waste. The 8-OHdG levels were detected at 6.40 +/- 1.64 mu mol/mol creatinine in preworkshift urines. However, the levels significantly increased to 24.55 +/- 5.96 mu mol/mol creatinine in postworkshift urines (p < 0.05). Then, it is concluded that there is a high cancer risk originated from oxidative stress indicated by the elevated 8-OHdG levels in the E-waste dismantling workers exposed to high concentrations of PCDD/Fs, PBDEs, and PCBs.
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Toll-like receptor 3 (TLR3) plays a key role in activating immune responses during viral infection. To study the genes involved in the regulatory function of TLR3 in the rare minnow Gobiocypris rarus after viral infection, a full-length cDNA of TLR3 (GrTLR3) with a splice variant (GrTLR3s) was identified by homologous cloning and RACE techniques. The antiviral effector molecule Mx gene was cloned and partially sequenced. The mRNA expression levels of GrTLR3, GrTLR3s, and Mx were studied in different tissues before and after virus infection by real-time quantitative RT-PCR. The transcripts of all three genes in liver were significantly increased following GCRV infection (P<0.05). The mRNA levels in liver were upregulated at 24 h post-injection for GrTLR3 and GrTLR3s, and at 12 h for Mx. The upregulated expression levels were several folds for GrTLR3s, tens of folds for GrTLR3, and hundreds of folds for Mx. By semi-quantitative RT-PCR, GrTLR3 and Mx expressed at all the developmental stages, whereas GrTLR3s could only be detected at later developmental stages. Using RNAi and transgenic techniques, GrTLR3 mediated Mx expression but GrTLR3s did not. The time-dependent upregulation of receptor and effector, and the Mx over-expression dependent on TLR3, indicated that GrTLR3 regulated Mx expression in viral infection through a configuration change in rare minnow, and its splice variant did not contribute to the process.
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Two MAbs (3C7 and 3C9) against flounder Paralichthys olivaceus rhabdovirus (PORV) were generated with hybridoma cell fusion technology and characterized by an indirect enzyme-linked immunosorbent assay, isotype test, Western blot and immunodot analysis and immunofluorescence assay. Isotyping tests demonstrated that both of the two MAbs belonged to IgM subclass. Western blot analysis showed the MAbs reacted with 42, 30, and 22 kDa viral proteins, which were localized within the cytoplasm of PORV-infected grass carp ovary (GCO) cells analyzed by indirect immunofluorescences tests. The MAb 3C7 was also selected at random for detecting virus antigens in the inoculated grass carp tissues by immunohistochemistry assay. Flow cytometry tests showed that at the 36 h postinfection (0.25 PFU/cell), the 23% PORV-infected GCO cells could be distinguished from the uninfected cells with the MAb 3C7. Such MAbs could be useful for diagnosis and potential treatment of viral infection. (C) 2007 Elsevier B.V. All rights reserved.