不同温度对中国对虾生长及能量收支的影响

研究了18～34℃6个不同恒温下中国对虾(Fenneropenaeus chinensis)的生长、饵料转化率及能量收支。结果表明,中国对虾的体重及能量特定生长率分别变动在1．22％～3．27％和1．33％～1．45％之间,在18～31℃温度范围内随温度升高而升高,34℃下则显著下降．对虾的摄食量及对饵料的消化率总体上随温度升高而升高,但在34℃下则有所降低;饵料重量转化率和能量转化率分别在28．99％～53．09％和15．70％～7．24％之间,总体上随温度升高而有所下降．根据拟合的多项式方程推算得到的中国对虾的最佳生长温度为29．7℃,生长能和呼吸能的变化主导着中国对虾的能量收支模式,随温度升高生长能占摄食能的比例逐渐降低,而呼吸能比例则逐渐升高。本研究表明,对虾在适宜温度下获得的较高生长率主要归因于较高的摄食量和食物消化率。     

恒温和变温下中国对虾生长和能量收支的比较

对比研究了模拟自然昼夜温度变化节律的4个变温(22±2)、(25±2)、(28±2)和(31±2)℃与相应的恒温22、25、28和31℃下中国对虾(F ennerop enaeus ch inensis O sbeck)生长和能量收支的差异。结果表明,对虾在(22±2)℃、(25±2)℃和(28±2)℃变温条件下的生长率显著高于相应的恒温,但(31±2)℃与恒温31℃相比没有显著差异。与相应的恒温相比,(25±2)℃、(28±2)℃和(31±2)℃变温下对虾的摄食量显著增大,(22±2)℃、(25±2)℃和(28±2)℃变温下对虾的饵料转化率则显著提高。但变温下对虾对食物的消化率与相应的恒温相比没有显著差异。能量收支研究结果则发现,(22±2)℃、(25±2)℃和(28±2)℃变温下对虾摄食能中,用于生长的能量比例显著增加,而(31±2)℃与31℃相比则未见显著差异。从而表明,变温促长的主要机制可归因于变温下摄食量的增大、饵料转化率的提高及其摄食能中用于生长能比例的增加。     

摄食水平对中华鳖稚鳖生长、氮排泄和能量收支的影响

在 30℃水温下进行摄食 -生长实验 (实验周期为 5 6d) ,设饥饿、1%、2 %、4 %和饱食 5个摄食水平 ,研究了中华鳖稚鳖 (39 5 4— 4 4 2 2g)的生长和能量收支。结果表明 ,中华鳖稚鳖的特定生长率随摄食水平的增加 ,其湿重、干物质、蛋白质和能量的特定生长率均呈二次曲线增加 ,其中干物质的特定生长率 (SGRdr)与摄食率 (Rl)的关系式为 :SGRdr=- 1 8799 1 0 795Rl- 0 0 832Rl2 (r=0 90 6 ,n =2 5 ,P <0 0 1) ;除干物质转化效率外 ,湿重、蛋白质和能量的转化效率在 2 %组均达到最大 ,分别为 36 31%、2 1 4 7%和 2 8 10 % ;除能量转化效率外 ,4 %组湿重、干物质和蛋白质的转化效率与最大值均无显著差异 ;摄食水平对中华鳖稚鳖总氮排泄率、氨氮排泄率、尿素氮排泄率以及氨氮占总氮排泄率的比例均有显著影响 (P <0 0 1) ,除氨氮占总氮比例外其他指标均随摄食水平的增加而增加 ,氨氮比例在饥饿组最高为 5 5 83% ,由饥饿到饱食其变化范围是 4 4 5 0 %— 5 5 83% ;总氮排泄率、氨态氮排泄率和尿素氮排泄率的变动范围分别是 19 81%— 6 5 87%、9 4 4 %— 36 31%和 8 2 4 %— 2 9 5 6 % ,回归分析表明 ,幼鳖的总氮排泄率 (μmol/g·d) (G N)、氨氮排泄率 (μmol/g·d) (NH3 N)及尿素氮排泄率 (μmol/g·     

Effect of ration and body size on the energy budget of juvenile white sturgeon

Growth and energy budget were measured for three sizes (2.4, 11.1 and 22.5 g) of juvenile white sturgeon Acipenser transmontanus held at 18.5° C and fed tubificid worms at different levels ranging from starvation to ad libitum . For each size-class, specific growth rate increased linearly with increasing ration, and conversion efficiency was highest at the maximum ration. Growth rate decreased with increasing fish size at the maximum ration, but increased with size at each restricted ration. Conversion efficiency increased with increasing ration for each size-class and was usually highest at the maximum ration. Faecal production accounted for 3.2–5.2% of food energy. The proportion of food energy lost in nitrogenous excretion decreased with increasing ration. With increases in ration, the allocation of metabolizable energy to metabolism decreased, while that to growth increased. Fish size had no significant effect on the allocation of metabolizable energy to metabolism or growth. At the maximum ration, on average 64.9% of metabolizable energy was spent on metabolism, and 35.1% on growth.     

中国明对虾AFLP分子标记遗传连锁图谱的构建

以中国明对虾抗WSSV(白斑综合症病毒,WhiteSpotSyndromeVirus)选育群体第四代为母本,野生中国明对虾为父本,采用单对杂交方式产生F1代,F1代个体姊妹交产生F2代共42个个体为做图群体。62对AFLP选择性引物组合共产生529个分离位点,符合1∶1孟德尔分离类型位点共253个,3∶1孟德尔分离类型位点共276个。利用拟测交理论分别构建中国明对虾雌虾、雄虾的遗传连锁图谱,利用F2自交模型构建共同的AFLP分子标记连锁图谱。三张连锁图上分别有31、25和44个连锁群,图谱分辨率为分别为2.4cM、2.4cM和2.1cM。标记间隔距离分别为12.20cM、11.45cM和11.12cM图谱覆盖率分别达到50.21%、51.93%和48.08%。能够基本满足进行QTL(数量性状位点,QuantitativeTraitLocus)定位的需要。将该图谱和其他对虾类遗传连锁图谱进行了比较分析,探讨了利用相关分子标记将已有图谱进行整合的可能。     

应用微卫星标记分析野生中国明对虾的亲权关系

利用5个高度多态性的微卫星座位(Fc04、Fc06、Fc18、Fc24、Fc27),分析了不同年份中建立的10个野生中国明对虾家系中的雌性亲虾及其后代基因型分离的情况,表明每个家系中只有一个雄性野生中国明对虾对子代的遗传有贡献.从其中3个家系的雌性亲虾纳精囊中提取了雄虾精子DNA,微卫星标记显示各家系的子代个体均有一个等位基因与雄性亲虾的基因型相符,且符合孟德尔遗传规律,这为野生中国明对虾雌虾在繁殖季节一对一的繁殖行为提供了遗传学的证据.用UPMGA的方法随机对3个家系的40尾子代个体进行聚类分析,每个家系都能被单独聚成一类.上述工作表明微卫星标记在对虾育种中作为一种有效的亲子关系分析工具,在种群的遗传结构、亲缘关系、繁殖行为等方面具有广阔的应用前景.     

中国明对虾过氧化物还原酶基因在大肠杆菌中的重组表达、产物纯化及活性测定

过氧化物还原酶（Prx）是生物体内广泛存在的一类酶,在消除过氧化氢和抗氧化胁迫中起着重要的作用。本研究采用PCR扩增编码中国明对虾Prx成熟肽的基因,并克隆到大肠杆菌表达载体pCR®T7/NT TOPO® TA中进行体外重组表达。重组质粒转化大肠杆菌BL21 (DE3) pLysS后,经IPTG诱导表达产生包涵体形式的目的蛋白。对重组蛋白进行LC–ESI–MS分析,结果表明融合蛋白的四个肽段与中国明对虾Prx相应肽段完全一致。将重组蛋白通过金属螯合柱进行纯化,进而透析、复性,最后获得了具有较高过氧化物酶活性的重组Prx。中国明对虾Prx的成功表达,为深入研究其在中国明对虾免疫反应和抗氧化胁迫中的作用奠定了基础。     

Effects of temperature, salinity, and fish size on growth and consumption of juvenile bluefish

Consumption and growth rates of juvenile bluefish Pomatomus saltatrix increased with increasing temperature and decreased with increasing fish size in short-term (7 days) experiments. Salinity had no effect on growth or consumption rate in a short-term experiment. In a long-term (90 days) mesocosm experiment, consumption and growth rates declined with increasing body size. Predictive equations developed from short-term experiments did not adequately predict observed consumption rates in the mesocosm experiment. However, growth in the mesocosm experiment was similar to field growth. Also, mesocosm consumption rates and consumption rates calculated using field growth and mesocosm growth efficiencies were similar to published independent field estimates of consumption rate. Our results indicate that experiments to determine the effects of temperature and the allometry of body size on growth and consumption rates should be conducted over long time periods simulating field conditions. Juvenile bluefish have rapid growth and their individual cumulative consumption is large. This result suggests that bluefish may have a large effect on their prey populations. This effect has yet to be quantified.     

Effects of salinity fluctuation on routine metabolism of juvenile spot, Leiostomus xanthums

We subjected juvenile spot, Leiostomus xanthurus , to eight different salinity fluctuation schedules to evaluate the effects of magnitude, rate, mean, and direction of salinity changes on their routine metabolism. Routine respiration stabilized within 3 h after all salinity changes and no fish died. Very rapid rates of change and changes at low mean salinity elicited short-term stress responses in 40–70 mm spot. Spot adapted more rapidly to increasing salinity changes than to decreasing changes, but the acclimation state of the fish apparently did not affect their salinity tolerance. Our results also indicated that spot undergo size-dependent changes in sensitivity to salinity fluctuation which correspond to seasonal shifts in distribution.     

EGFP基因在中国明对虾原代培养细胞中的导入和表达

本文以我国重要水产养殖动物中国明对虾（Fenneropenaeus chinensis）贴壁培养和悬浮培养的血细胞、植块培养的类淋巴器官（Oka器官）细胞和卵巢细胞为材料,通过磷酸钙共沉淀法、脂质体介导的转染（脂染）和电穿孔法等多种方法进行了导入EGFP基因的实验。结果表明,通过脂染可以成功地将质粒DNA导入悬浮培养的血细胞、植块培养的Oka器官细胞和卵巢细胞,并使报告基因EGFP得到表达。