山溪性可冲性强潮河口曹娥江高水位初步研究

应用多年的实测资料 ,分析了曹娥江河口高水位成因 ,结果表明 ,曹娥江河口洪水位具有山溪性和可冲性的特点 ,人类活动对高水位有较大影响。应用统计分析法和成因分析法推求 1 %设计高水位 ,讨论了成因分析法中上、下边界条件的选取 ,其选取原则对其他潮汐河口确定设计高水位具有借鉴意义     

On dynamic coupling effects between a spar and its mooring lines

The responses of a spar constrained by slack mooring lines to steep ocean waves and tensions in the mooring lines are simulated using two different numerical schemes: a quasi-static approach (SMACOS) and a coupled dynamic approach (COUPLE). The two approaches are the same in computing wave loads on the structure. Their difference is in modeling dynamic forces of mooring lines; that is the dynamic forces are included in the computation of COUPLE but neglected in SMACOS. The numerical simulation is examined against the laboratory measurements of the JIP Spar in a water depth of 318 m. The dynamic coupling effects between the JIP Spar and its mooring lines in different water depths (318, 618 and 1018 m) are investigated by the comparison of numerical simulations obtained using the quasi-static and coupled dynamic approaches. It is found that the damping of mooring lines reduces the slow-drift surge and pitch of the Spar, especially in deep water. The reduction in the amplitude of slow-drift surge can reach about 10% in a water depth of 1018 m. The tension in mooring lines may greatly increase in the wave frequency range when dynamic forces in mooring lines are considered. The mooring-line tension in the wave frequency range predicted by the coupled dynamic approach can be eight times as great as the corresponding prediction by the quasi-static approach in a water depth of 1018 m. This finding may have important implications for the estimation of the fatigue strength and life span of the mooring lines deployed in deep water oceans.     

Parameterization of Wave Breaking Probability and Whitecap Coverage

1 .Introduction Wave breaking and associated whitecapping have long beeninteresting due totheir close relationto many fields of ocean study,including air-sea interaction,remote sensing,ocean engineering,aswell as wave dynamics .The breaking probabilityBan…     

GPS测高技术在无验潮水深测量中的应用

应用双频GPS动态后处理高精度定位技术，建立了一套完整的GPS无验潮海洋深度测量作业模式，通过海上试验与传统作业模式作了数值分析比较，结果表明，该作业模式不仅无需验潮，而且能够有效消除传统作业模式中船只动态吃水和涌浪等因素对测量成果的影响，显著提高水深测量成果的精度。     

双层局部开孔板沉箱对波浪反射的理论研究

提出了一种用于研究由双层开孔板和一个不透水后板的开孔结构对斜向波反射率的理论分析方法。整个流域被分成三个子域，在每个子域内应用特征函数展开法以得到该域内包含未知展开系数的势函数的表达式，在速度势的展开中，考虑了非传播模态波浪的影响。通过匹配开孔板处的边界条件可以求解待定的展开系数，继而求解双层开孔板防波堤结构对斜向波的反射率。数值计算结果与试验结果进行了比较，符合较好。并进一步讨论了几个重要因素对反射系数的影响。     

凡纳滨对虾高密度养殖实验

实验时间 4 0天 ,放苗密度 5 0 0尾 /m2 、10 0 0尾 /m2 。凡纳滨对虾初体长为 2 .5 88±0 .341cm ,初体重 (0 .2 39± 0 .0 86 ) g。养殖水体中放置筛绢隔断 ,在不换水的条件下 ,监测水体中无机磷、氨氮的变化趋势 ,初步实验高密度和分隔养殖的效果。结果表明 ,高、低密度氨氮、无机磷差异均为极显著 (P <0 .0 1) ;成活率、产量差异均为显著 (P <0 .0 5 )。高、低密度特定生长率 体重 差异不显著 (P >0 .0 5 )。观察到不同时间不同密度凡纳滨对虾对筛绢隔断的反应不同 ,表明对虾能利用隔断筛绢 ,从而有效提高养殖容量     

健康型牛蛙饲料养殖牛蛙的试验

本研究采用5种中草药添加剂配方的膨化饲料进行了为期36d的牛蛙养殖对比试验.结果表明，饲料中添加有中草药制剂的日摄食量明显大于对照组，日增重显著比对照组的高.而且大大加快了生长速度，缩短养殖周期，同时减少了染病机率，牛蛙体色鲜艳、光泽度极佳.     

NUMERICAL EXPERIMENTS OF WINDS OVER THE NORTHERN PACIFIC OCEAN WITH NONLINEAR DIAGNOSTIC DYNAMIC MODEL

By means of the proposed nonlinear diagnostic dynamic model for the planetary boundary layer (PBL) wind field, an introduction is given to the MOD method for wind prediction. Based on the MOD experiments on the surface wind field over the Northern Pacific Ocean from April to October 1985, it is concluded that the nonlinear diagnostic dynamic model used is better than the linear one.     

海湾扇贝养殖群体遗传多样性的研究

用等位基因酶的聚丙烯酰胺凝胶电泳技术,研究了大连沿岸不同生态环境条件下的大李家湾低排筏、大李家湾高排筏、凌水桥、棋盘磨4个海湾扇贝养殖群体的遗传多样性.在4个群体的7种等位基因酶和闭壳肌蛋白中均检测到了22个基因位点,各群体的多态位点比例分别为22.73%,22.73%,22.73%,18.18%(P≤0.95)和27.27%,27.27%,31.82%,36.36%(P≤0.99);杂合度观测值分别为0.064,0.071,0.075,0.069;Hardy-Weinberg平衡偏离指数分别为-0.068,-0.020,-0.032,-0.050;近交系数分别为0.568,0.565,0.487,0.550;位点等位基因有效数分别为1.102,1.109,1.143,1.122;遗传变异综合评价指数分别为0.0060,0.0071,0.0088,0.0073.海湾扇贝养殖群体遗传多样性总体水平较低,但在这4个群体中,凌水桥群体的遗传多样性水平最高,大李家湾高排筏和棋盘磨群体的遗传多样性水平较高,大李家湾低排筏群体遗传多样性水平最低.     

6-磷酸山梨醇脱氢酶(gutD)基因克隆、测序和表达

本研究根据6-磷酸山梨醇脱氢酶基因(gutD)两端序列设计引物，以假单胞杆菌(Pseudonmonas XM)的总DNA为模板通过PCR的方法克隆gutD基因并进行序列分析，将克隆得到的gutD基因与原核表达载体pBV220连接并转化大肠杆菌(Escherichia coli)JM101后检测其蛋白表达及菌株生长耐盐性。