基于小波变换选择的海底沉积物声速分析技术

海底沉积物物理特性参数的研究对海洋资源开发、海底工程建设、海地测绘、海洋灾害预报、海底历史研究、航运国防等具有重要意义.它可由对出海采样的样品直接进行土工实验获取,或者经测量得到的声学特性参数表征.目前海底沉积物探测主要以声学测量为主,通过接收透射、反射、折射的声波后提取出声学特性而成,包括压缩波速、切变波速(液体不存在)、声波阻抗、声衰减.针对传统的走时法由于人工读取起跳点造成声速的精确度不高这一特点,引出小波分析方法读取起跳点,应用小波分解原始信号得到的细节信号的模极大值连线来确定原始信号的畸变点,从而确定为接收声信号的起跳点以计算声速.     

脂肪肝病变大黄鱼肝脏脂肪酸组成、代谢酶活性及抗氧化能力的研究

脂肪肝病变在人工养殖大黄鱼(Pseudosciaena crocea)中非常普遍,本试验研究了大黄鱼脂肪肝的发生机制,为寻找解决大黄鱼脂肪肝的有效途径提供基础资料.试验鱼取自中国东海,养殖方式和饲料来源相同,根据肉眼和组织学观察分为正常肝脏、轻微脂肪肝和严重脂肪肝3类.分别测定了正常大黄鱼和具有脂肪肝症状的大黄鱼肝脏总脂脂肪酸组成的变化、相应脂肪酸合成酶、抗氧化酶以及丙二醛含量的变化.试验结果显示,随着大黄鱼脂肪肝症状严重程度增加,肝脏总脂饱和脂肪酸和n-3多不饱和脂肪酸比例显著降低(P<0.05),单不饱和脂肪酸比例显著上升(P<0.05).其中严重脂肪肝花生四烯酸(ARA)、二十碳五烯酸(EPA)、二十二碳六烯酸(DHA)比例较正常鱼分别降低了89%,79%和78%.严重脂肪肝大黄鱼的异柠檬酸脱氢酶和6-磷酸葡萄糖脱氢酶活性显著高于正常鱼(P<0.05);轻微脂肪肝鱼的转氨酶活性显著低于正常鱼(P<0.05);具有脂肪肝症状的大黄鱼超氧化物歧化酶和过氧化氢酶活性均高于正常鱼.丙二醛含量则随大黄鱼脂肪肝病变程度加剧而显著增加(P<0.05).通过分析认为,过量单不饱和脂肪酸沉积在肝脏中,导致脂肪酸合成代谢发生紊乱,可能是造成大黄鱼脂肪肝的主要原因;肝脏ARA含量大量减少使脂肪肝大黄鱼抗应激能力降低,而肝脏脂肪酸过氧化程度升高,进一步破坏肝脏的正常功能.     

椒江口潮间带大型底栖动物群落beta多样性分析

于2007年10月在椒江口共布设6条潮间带采样断面,每条断面在中潮带上区、中区、下区和低潮区各设1站位进行大型底栖动物采样。分析了不同采样站位数与大型底栖动物种数的关系,选用Wilson-Shmidabeta多样性测度方法,对以下3种空间环境梯度下大型底栖动物群落beta多样性进行了研究:(1)断面内垂直环境梯度;(2)河流到海洋的环境梯度;(3)河口两岸间的距离梯度。分析了不同采样站位数对群落beta多样性指数的影响,结果显示:(1)随着采样站位数的增加,物种数呈增加趋势但增速渐慢,同时beta多样性指数呈下降趋势;(2)不同的潮区间隔下的be-ta多样性指数均有显著差异;(3)在北岸和南岸,随着断面间距的增加beta多样性指数均呈升高趋势,而且与各断面的沉积物粒度、油类含量呈显著相关;(4)椒江口为喇叭形河口,随着河口两岸断面距离的增加beta多样性指数呈升高趋势。     

应用巢式逆转录聚合酶链反应检测鱼类病毒性出血性败血症病毒(VHSV)

参照鱼类病毒性出血性败血症病毒序列,根据PCR引物设计的原则,设计巢式PCR引物,采用巢式逆转录聚合酶链反应(RT-PCR)方法,对如何快速检测鱼类病毒性出血性败血症病的方法进行了较为系统的研究,并对RT-PCR的反应条件进行了优化.结果表明,巢式RT-PCR扩增获得279bp的特异性片断,阴性对照无扩增条带.巢式RT-PCR扩增出的特异性片段经测序分析,结果证实与报道的序列完全一致.该方法最低可检测出0.1pg的鱼类病毒性出血性败血症病毒RNA.初步建立了VHSV的巢式RT-PCR检测方法,该方法灵敏、特异,可为VHSV的检测提供一个快速、有效的手段.     

侧扫声纳在水下坡脚线位置探测中的精度分析

根据国家海洋局印发的《海籍调查规范》,填海工程用海范围算至填海边坡水下坡脚线。在填海工程竣工验收中,水下坡脚线主要使用侧扫声纳获取。通过对侧扫声纳探测水下坡脚线位置的误差来源进行分析,提出了一系列提高侧扫声纳水下坡脚线位置探测精度的措施,并将其应用到实际工作中,对侧扫声纳水下坡脚线位置探测精度进行了验证。结果表明,侧扫声纳在填海工程水下坡脚线探测中的位置精度满足《海籍调查规范》中水下坡脚线平面位置精度要求。     

南麂岛附近海域潮汐和潮流的特征

以2008年冬季在浙江近海南麂岛附近投放的4个底锚系观测的水位和流速资料为依据,分析了潮汐和潮流特征。水位谱分析结果显示半日分潮最显著,全日分潮其次;近岸的浅水分潮比离岸大。水位调和分析结果表明:潮汐类型均为正规半日潮,近岸处的平均潮差大于3m,最大可能潮差大于6m,潮汐呈现出显著的低潮日不等和回归潮特征。流速谱分析结果显示半日分潮流最强,全日分潮流其次,且比半日分潮流小得多;近岸浅水分潮流比远离岸显著。流速调和分析结果表明:潮流类型均为正规半日潮流,靠近岸的两个站浅水分潮流较显著;最显著的半日分潮流是M2分潮流,其最大流速介于0.32～0.48m/s之间,全日分潮流均很弱,最大流速小于0.06m/s。M2分潮流均为逆时针旋转,椭圆率越靠近海底越大;最大分潮流流速分布为中上层最大、表层略小、底层最小;最大分潮流流速方向的垂向变化很小,底层比表层略为偏左;最大分潮流流速到达时间随深度的加深而提前,底层比中上层约提前30min。潮流椭圆的垂向分布显示这里的半日分潮流以正压潮流为主;日分潮流则表现出很强的斜压性。     

基于EMD的中国大陆强震活动特征分析

利用EMD方法对中国大陆年度最大地震时间序列进行逐级分解, 得到5个本征模态函数(IMF)项和1个趋势项, 分析了各个IMF分量不同的周期成分同地球自转速度变化、 太阳黑子活动和潮汐运动等环境因子之间的相关关系, 初步探讨了各个IMF分量的物理机理及其对中国大陆地震活动的影响。     

西太平洋深海海水中乙醛降解菌多样性及群落结构研究

As a major aldehyde pollutant widely existing in industry and our daily life, acetaldehyde is more and more harmful to human health. As characteristic habitat niche, bacteria from deep sea environments are abundant and distinctive in heredity, physiology and ecological functions. Thus, the development of acetaldehyde-degrading bacteria from deep sea provides a new method to harness acetaldehyde pollutant. Firstly, in this study,acetaldehyde-degrading bacteria in the deep sea water of the West Pacific Ocean were enriched in situ and in the laboratory respectively, and then the diversity of uncultured bacteria was studied by using 16 S r RNA genes. Then acetaldehyde-degrading strains were isolated from two samples, including enrichment in situ and enrichment in laboratory samples of deep sea water from the West Pacific Ocean using acetaldehyde as the sole carbon source,and then the ability of acetaldehyde degradation was detected. Our results showed that the main uncultured bacteria of two samples with different enrichment approaches were similar, including Proteobacteria,Actinobacteria, Firmicutes, Cyanobacteria, but the structure of bacterial community were significant different.Four subgroups, α, γ, δ and ε, were found in Proteobacteria group. The γ-Proteobacteria was dominant(63.5%clones in laboratory enriched sample, 75% clones in situ enriched sample). The species belonged to γ-Proteobacteria and their proportion was nearly identical between the two enrichment samples, and Vibrio was the predominant genus(45% in laboratory enriched sample, 48.5% in situ enriched sample), followed by Halomonas(9% in situ enriched sample) and Streptococcus(6% in laboratory enriched sample). A total of 12 acetaldehyde-degrading strains were isolated from the two samples, which belonged to Vibrio, Halomonas,Pseudoalteromonas, Pseudomonas and Bacillus of γ-Proteobacteria. Strains ACH-L-5, ACH-L-8 and ACH-S-12,belonging to Vibrio and Halomonas, have strong ability of acetaldehyde degradation, which could tolerate 1.5 g/L acetaldehyde and degrade 350 mg/L acetaldehyde within 24 hours. Our results indicated that bacteria of γ-Proteobacteria may play an important role in carbon cycle of deep sea environments, especial the bacteria belonging to Vibrio and Halomonas and these strains was suggested for their potentials in government of aldehyde pollutants.     

Enhanced a novel β-agarase production in recombinant Escherichia coli BL21(DE3) through induction mode optimization and glycerol feeding strategy

Agarases are hydrolytic enzymes that act on the hydrolysis of agar and have a broad range of applications in food,cosmetics and pharmaceutical industries. In this study, a glycerol feeding strategy based on induction mode optimization for high cell density and β-agarase production was established, which could effectively control acetate yield. First, exponential feeding strategy of glycerol with different overall specific growth rates(μ) was applied in the pre-induction phase. The results showed that the low μ(μ=0.2) was suggested to be the optimal for cell growth and β-agarase production. Second, the effects of induction temperature and the inducer concentration on cell growth and β-agarase production were investigated in the post-induction phase. When induced by isopropyl-β-d-thiogalactoside(IPTG), the strategy of 0.8 mmol/L IPTG induction at 20℃ was found to be optimal for β-agarase production. When cultivation was induced by continuous lactose feeding strategy of 1.0 g/(L·h), the β-agarase activity reached 112.5 U/mL, which represented the highest β-agarase production to date.Furthermore, the β-agarase was capable of degrading G. lemaneiformis powder directly to produce neoagarooligosaccharide, and the hydrolysates were neoagarotetraose(NA4) and neoagarohexaose(NA6). The overall research may be useful for the industrial production and application of β-agarase.     

一种新型张力保护自动收放脐带缆绞车装置

介绍一种新型张力保护自动收放的脐带缆绞车装置的组成及特点。该装置克服了传统脐带缆绞车全人工操作模式所存在的效率低和安全性差等问题,实现了脐带缆绞车的自动收放和排缆,准确控制脐带缆张力,有效保护脐带缆的安全,大幅提高了潜水器等水下作业设备的工作效率和作业安全性。