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1.
病毒是非常微小的简单生物, 不能独立生存, 必须借助宿主细胞完成自身的繁衍。病毒侵染进入细胞后, 通常借助于微管通过黏稠的细胞质运动到特定的复制位点。然而, 有关病毒依赖微管运动行为的精细动态研究还比较少。石斑鱼虹彩病毒(Singapore grouper iridovirus, SGIV)为虹彩病毒科蛙病毒属的一个新种, 是海水养殖鱼类的重要病毒性病原, 对海水养殖业造成重大经济损失。利用单粒子示踪技术实时追踪了SGIV病毒粒子沿微管运动的行为, 观察到SGIV在细胞边缘至微管中心之间的双向运动, 最高瞬时速度约0.2μm·s-1, 均表现为主动运输。病毒粒子运动至微管交叉位置会减速迂回, 而后或受限于此, 平均运动速率约0.008μm·s-1, 或通过交叉处继续快速运动, 最高瞬时速度为0.2μm·s-1。同时, SGIV感染会影响微管的形态结构, 随着SGIV感染, 微管逐渐围绕细胞核和病毒加工厂形成环状结构。研究结果初步揭示了SGIV病毒和细胞微管之间相互作用的复杂过程, 丰富了我们对虹彩病毒胞内生命活动的认识, 有助于深入地理解海水鱼类虹彩病毒感染致病机理。  相似文献   
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The disease resistance and humoral immunomodulatory effects of vitamin C administered orally to grouper,Epinephelus awoara maintained on a frozen fish diet supplemented with vitamin C at 500, 1000, 1500 and 2000 mg/kg were investigated. After 20 weeks, the growth rates of the groups with high level of vitamin C apparently increased. The untreated fish had symptoms of vitamin C deficiency. The endogenous liver tissue vitamin C levels were found to reflect well the dietary treatments. After intraperitoneal injection or bath challenge with a virulent strain ofVibrio vulnificus, fish fed with high level vitamin C showed significantly higher survival rate compared with the normal control group. Vaccination with formalin inactivatedV. vulnificus significantly enhanced the specific antibody production in fish treated with vitamin C, and completely protected from strong bacterial challenge the groups fed on fish with vitamin C 1500 and 2000 mg/kg diet. Project 39500113 supported by NSFC and also by Guangdong Science Research Foundation (Grant No. 950711).  相似文献   
4.
Effects of water temperature (17, 21, 25, 30 and 35℃) and body size (14.75-281.41 g initial body weight) on food consumption, growth, feed conversion, and dry matter content in orange-spotted grouper fed to satiation were investigated. The combined effect of temperature (T, ℃) and body weight (W, g) on maximum food consumption (Cmax, g/day) was described as: InCmax=-7.411+0.828 InW+0.317T4).004 7T2, and the optimum feeding temperature was 33.9℃. The combined effect of temperature and body weight on growth (G) was described as: lnG=-4.461-0.2081nW+0.394T-0.006 3T^2. The optimum growth temperature was 31.4℃, whereas overall growth rates were high at 25, 30 and 35 ℃. Feed conversion efficiencies (FCE, %), increasing first and then decreasing with increasing temperature, averaged from 1.8 to 2.1 in terms of dry weight of food fish. The optimum temperature for FCE tended to be lower than that for growth or feeding. Dry matter content increased with both increasing water temperature (17, 25, 30 and 35℃) and body weight, and the combined effect of temperature and body weight on dry matter content (DM, %) was described as: lnDM =3.232+0.01 4 lnW-0.004 4T+0.001 2TInW.  相似文献   
5.
The paper reviews the recent advances in studying grouper nutrition requirement for the development of cost-effective and environmentally friendly artificial diets. It consists of seven parts: protein and amino acid, lipid and essential fatty acid, carbohydrate, vitamin, mineral, alternative protein source, broodstock and larval nutrition. The review provides some basic information for further investigation of nutrient requirements of groupers.  相似文献   
6.
对赤点石斑鱼(Epinephelus akaara)精子的激活特点、超低温冷冻方案筛选、短期保存、受精实验等方面进行了研究。结果表明:水温25℃、比重为1.018的海水对赤点石斑精子具有最佳的激活效果,活力为(82.50±4.18)%;在进行超低温冷冻时,选择距离液氮面7 cm的高度进行降温,获得冻后活力为(65.83±3.76)%,显著高于1、3、15 cm 的处理组(P<0.0001),利用冻存液 B(含30 g/L 海藻糖、10%DMSO 的生理盐水)冻存赤点石斑精子,冻精活力为(67.92±3.96)%,显著高于另外两种冻存液(P<0.05);通过优化的方案(冻存液B,7 cm高度)冻存得到精子可获得较好的受精效果,受精率为(74.55±4.31)%,而相应的鲜精受精率可达(87.42±4.63)%,二者间的差异具有显著性(P=0.017);短期保存的结果表明,赤点石斑鱼精子在4℃环境中保存约两周后活力降低为0。  相似文献   
7.
Small-scale fisheries are often seen as a solution for ensuring sustainability in marine exploitation. They are viewed as a suitable alternative to industrial fisheries, particularly when considering their social and economic importance in developing countries. Here, we show that the booming small-scale fishery sector in Senegal, in the context of increasing foreign demand, has induced the collapse of one of the most emblematic West African marine fish species, a large grouper Epinephelus aeneus, historically called ‘false cod’ by European fishers. The overexploitation of this species appears to be on account of the increasing effort sustained by a growing international demand and important subsidies, which resulted in a relative stability of the average economic yield per fishing trip and an incentive for continuing targeting this species to almost extinction. It is a critical time for addressing and mitigating the pressure of the small-scale fisheries to prevent declines of fish species that are highly valued by northern markets. A balance between conservation and exploitation is necessary to maintain ecological viability while considering the socio-economic importance of the small-scale fisheries. However, a new strategy is needed for conservation that will consider and articulate simultaneously the concerns regarding unmanaged and growing small-scale fisheries, rampant subsidies and increasing foreign demand.  相似文献   
8.
采用RT-PCR方法克隆了斜带石斑鱼两种催乳素受体(Prolactin receptor,PRLR)的cDNA序列,序列分析表明:PRLR1开放阅读框为1947bp,共编码649个氨基酸,PRLR2开放阅读框为1749bp,共编码487个氨基酸,PRLR1与PRLR2的氨基酸同源性为40.4%。用Real-time RT-PCR方法研究了PRLR1和PRLR2在各组织和早期发育不同阶段的表达情况,结果表明:PRLR1和PRLR2在所检测的12种组织中均有表达,其中以鳃、肾、肠表达量较高;PRLR1在受精期表达最高,PRLR2在视囊形成期表达最高,而且除受精卵期外PRLR2在各时期的表达量均高于PRLR1。  相似文献   
9.
龙虎斑是由棕点石斑鱼(Epinephelusfuscoguttatus♀)和鞍带石斑鱼(Epinepheluslanceolatus♂)的杂交种。研究水温及盐度在骤变和渐变情况下龙虎斑的存活和摄食情况,结果表明:龙虎斑在温度为1435℃的海水中均能存活和摄食,最适宜温度环境为2535℃的海水中均能存活和摄食,最适宜温度环境为2535℃;温度从30℃骤变至20、25、35℃时,龙虎斑100%存活;从30℃骤变至10℃和15℃时,龙虎斑全部死亡;水温从30℃开始渐变,下降幅度为1℃/d,当下降至24℃时摄食减少,13℃时停止摄食,下降至11℃时出现死亡。龙虎斑在盐度为135℃;温度从30℃骤变至20、25、35℃时,龙虎斑100%存活;从30℃骤变至10℃和15℃时,龙虎斑全部死亡;水温从30℃开始渐变,下降幅度为1℃/d,当下降至24℃时摄食减少,13℃时停止摄食,下降至11℃时出现死亡。龙虎斑在盐度为155的海水中均能存活和摄食,摄食适宜海水盐度为455的海水中均能存活和摄食,摄食适宜海水盐度为445;盐度从30骤变至5、10、15、20、25、35、40、45、50、55等盐度时,龙虎斑100%存活,骤变至0时,4 h内存活率100%,16 h存活率55.5%;盐度从30渐变,每天降低2,降至6后,每天降低1,盐度降到1时,龙虎斑的活动和摄食明显减少,渐变至0时,36 h出现死亡,48 h内全部死亡。  相似文献   
10.
将新加坡石斑鱼虹彩病毒(Singapore grouper iridovirus,SGIV)的ORF162的开放式阅读框插入pET-32a表达载体T7启动子控制下的6-His·Tag编码基因上游,构建SGIVORF162原核表达质粒pET-ORF162。表达质粒转化入大肠杆菌BL21(DE3)菌株,经IPTG诱导,成功表达SGIV ORF162融合蛋白。对IPTG浓度、诱导温度、诱导时间等诱导表达条件进行优化后,确定在0.7mmol/LIPTG、16℃条件下诱导14h时可溶性SGIV ORF162重组蛋白占重组蛋白总量的95%。经镍琼脂糖凝胶纯化,获得纯度为90%以上的SGIV ORF162蛋白。用纯化的SGIV ORF162蛋白免疫小鼠,获得高效特异的SGIV ORF162多克隆抗体。  相似文献   
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