988 resultados para 302-M0003A
Resumo:
This paper is aimed at enabling the confident use of existing model test facilities for ultra deepwater application without having to compromise on the widely accepted range of scales currently used by the floating production industry. Passive line truncation has traditionally been the preferred method of creating an equivalent numerical model at reduced depth; however, these techniques tend to suffer in capturing accurately line dynamic response and so reproducing peak tensions. In an attempt to improve credibility of model test data the proposed truncation procedure sets up the truncated model, based on line dynamic response rather than quasi-static system stiffness. The upper sections of each line are modeled in detail, capturing the wave action zone and all coupling effects with the vessel. These terminate to an approximate analytical model that aims to simulate the remainder of the line. Stages 1 & 2 are used to derive a water depth truncation ratio. Here vibration decay of transverse elastic waves is assessed and it is found that below a certain length criterion, the transverse vibrational characteristics for each line are inertia driven, hence with respect to these motions the truncated model can assume a linear damper whose coefficient depends on the local line properties and vibration frequency. Stage 3 endeavors to match the individual line stiffness between the full depth and truncated models. In deepwater it is likely that taut polyester moorings will be used which are predominantly straight and have high axial stiffness that provides the principal restoring force to static and low frequency vessel motions. Consequently, it means that the natural frequencies of axial vibrations are above the typical wave frequency range allowing for a quasi-static solution. In cases of exceptionally large wave frequency vessel motions, localized curvature at the chain seabed segment and tangential skin drag on the polyester rope can increase dynamic peak tensions considerably. The focus of this paper is to develop an efficient scheme based on analytic formulation, for replicating these forces at the truncation. The paper will close with an example case study of a single mooring under extreme conditions that replicates exactly the static and dynamic characteristics of the full depth line. Copyright © 2012 by the International Society of Offshore and Polar Engineers (ISOPE).
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硫酸铜广泛用于水华藻类的去除和控制。本文测定了不同藻类对Cu2+的敏感性,几种常见水华藻类对Cu2+的敏感性顺序为:铜绿微囊藻>水华鱼腥藻>小环藻>莱哈衣藻>斜生栅藻。在某城市的富营养化湖泊中用Cu-SO4.5H2O(102μg/LCu2+)作为杀藻剂控制蓝藻水华的试验结果表明:在用硫酸铜控制蓝藻水华的过程中,水体透明度有明显改善;总氮总磷无显著变化;浮游植物总数在试验初期下降,但在试验后期则有所回升,在试验初期蓝藻门数量有所下降,绿藻门和硅藻门数量增加,这与不同藻类对Cu2+敏感性差异相关;试验后期,蓝
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在本研究中,将福尔马林灭活的柱状黄杆菌菌苗(FKG4)经腹腔注射免疫草鱼,以注射灭菌PBS作对照,分别在免疫后1、7、15和28d,提取受免鱼和对照鱼肝脏、脾脏和头肾3种组织中的总RNA并反转录成cDNA,利用Real-time PCR方法对不同组织中C-反应蛋白(CRP)、主要组织相容性复合体I(MHCⅠ)、肿瘤坏死因子(TNFα)、白介素1(IL-1β)、白介素8(IL-8)、Ⅰ型干扰素(IFNⅠ)等6种免疫相关基因的表达进行定量分析。结果发现CRP在受免鱼肝脏中的表达于免疫后1、7d显著高于对照鱼,
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首次报道了亚东鲑在青藏高原河流中的生长特点。对1999—2002年间在亚东河共采集的462尾亚东鲑(体长范围为93—364mm)进行了年龄与生长的研究。通过鳞片对其中302尾进行年龄鉴定并建立Von Bertalanffy生长方程:雌性(♀)Lt=709.44[1-e-0.1656(t-0.0845)](R2=0.9993,n=132)和Wt=6017.46[1-e-0.1656(t-0.0845)]2.9724(R2=0.9845,n=132);雄性(♂)Lt=797.82[1-e-0.1428(t-0
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用噬菌体展示技术制备了抗对虾白斑综合症病毒(WSSV)的单链抗体A1。该抗体在30℃培养条件下诱导表达20h后,其蛋白表达量可达总菌体蛋白的3.67%。用亲和层析柱和SephadexG-100层析柱可将单链抗体A1纯化为一条单电泳条带,其分子量约为31.5kD。用等电聚焦电泳测定,其等电点为pH5.8。ELISA测定表明冻干的单链抗体A1在室温储藏4年后与WSSV结合仍具有较高的活力。
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将柱状黄杆菌胞外多糖(EPS)溶液经腹腔注射免疫草鱼,以注射灭菌生理盐水作对照。免疫一周后,分别提取受免鱼与对照鱼肝脏、脾脏、体肾和头肾4种组织中的总RNA,并通过RT-PCR半定量的方法检测不同组织中C-反应蛋白(CRP)、白介素1(IL-1)、主要组织相容性复合体I(MHC I)、免疫球蛋白M(IgM)、干扰素(IFN)等5种免疫基因的表达情况。结果显示,CRP在受免鱼肝脏中的表达显著上升;MHC I在受免鱼脾脏、体肾中的表达显著下降;IgM在受免鱼4种组织中的表达皆显著上升;IL-1在受免鱼4种组织
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流式细胞术做为一种高新生物技术,在动物医学的各个领域,包括细胞生物学、病毒学、肿瘤学、免疫学和病理学中都得到广泛应用,为细胞凋亡研究提供了有效的技术手段。该技术具有简便、快速、多参数分析等优点,可针对细胞在凋亡时产生的一系列形态学、生物化学及分子生物学性质的变化,包括细胞皱缩,核染色质凝聚,细胞膜通透性改变,Caspases 激活,线粒体跨膜电位降低,膜磷酯酰丝氨酸外化,胞质 Ca2+ 浓度升高,DNA片段化及含量变化等特点,进行定性、定量测试分析,从而实现对细胞凋亡的准确测定。
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属于虹彩病毒科的淋巴囊肿病毒(Lymphoeystisdiseasevirus,LCDV)是一类能引起全球各地上百种淡、海水鱼产生囊肿的病原。在新分离到淋巴囊肿病毒中国株(LymphocystisdiseasevirusisolatefromChina,LCDV—C)并完成序列测定的基础上,用计算机辅助分析了LCDV—C羟类固醇脱氢酶(hydroxysteroiddehydrogenase,HSD)基因结构特征,LCDV—CHSD读码框为1023bp,推导其编码含340个氨基酸、分子量约为39.3kD的蛋