关于Barban定理的推广

本文将Barban定理中和式形式加以推广,得到关于函数μ(n)的这种和式的估计。     

鮸鱼胚胎发育的研究

研究了人工繁殖时鮸鱼(Miichthys miiuy)胚胎的发育过程。鮸鱼受精卵呈圆球形,浮性,卵径为0.99~1.15 mm,中央大多具有1个油球,少数为2~3个或较多个油球。在水温为24.5~24.7℃,盐度为24的天然海水中,鮸鱼胚胎发育历时约21h 48 min孵化出膜。整个胚胎发育分为5个阶段,共21个发育期。     

I(L)值完全诱导空间

作者引入 I(L)值完全下半连续映射 ,研究其性质。利用 I(L)值完全下半连续映射定义I(L)值完全诱导空间 ,给出 I(L)值完全诱导空间的拓扑基的表达形式 ,证得两个 I(L)值完全诱导空间的映射是连续映射的充分必要条件 ,并建立了乘积空间的 I(L)值完全诱导空间与 I(L)值完全诱导空间的乘积空间的联系     

舒曼海山铁锰结壳中钙质超微化石生物地层的年龄测定

用钙质超微生物地层学确定夏威夷考爱岛以北200英里，舒曼海山铁锰结壳内不同层次的年龄和生长速率．这项工作是利用不同地球化学指示物重现结壳古海洋历史研究的一部分．     

细菌、病毒与浮游植物相互关系及其对海洋地球化学循环的作用

本文综述了近年来国内外在海洋地球化学循环，特别是微生物环研究方面的发展现状，探讨了浮游植物，细菌，病毒相互之间的关系及其对海洋地球化学循环的影响。     

化学物质对硬壳蛤幼虫变态的诱导

用KCl、肾上腺素（EPI）、去甲肾上腺素（NE）、L—DOPA和GABA（γ-氨基丁酸）进行了不同浓度不同处理时间对硬壳蛤（Mercenaria mercenaria L ）幼虫变态诱导实验。结果表明，KCl、肾上腺素、去甲肾上腺素和DDOPA对硬壳蛤幼虫的变态均有诱导作用，而GABA的诱导作用不显著。KCl的最佳诱导浓度随处理时间不同而有所不同。处理时间为1～24，48，72h时KCl的最佳诱导浓度分别为33．56，20．13～26．85，13．42mmol／L。肾上腺素和去甲肾上腺素的诱导作用与浓度和处理时间均有关。肾上腺素的最佳处理浓度为100μmol／L，最佳处理时间均为8h，此时幼虫变态率提高最大，为36．97个百分点。当去甲肾上腺素的诱导浓度为100μmol／L，处理时间为8～16h时，幼虫变态率提高也较大，均大于18个百分点，死亡率增加，但均低于30个百分点，当去甲肾上腺素诱导浓度为500μmol／L时，虽然在8～16h的处理时间范围内，幼虫变态提高率也较大，均大于18个百分点，但当处理时间超过8h，在16～48h范围内，幼虫死亡率提高明显增大，均大于50个百分点。L-DOPA的适宜诱导浓度为10～50μmol／L，适宜处理时间为8～24h，此时幼虫变态率均提高30个百分点以上，最高可提高79．43个百分点。GABA的诱导作用较弱，最佳诱导浓度随处理时间的不同而有所不同，处理时间为24h和48h时，最佳诱导浓度为0．1μmol／L；处理时间为0．5～16h时，最佳诱导浓度为100μmol／L。     

Diagnosis of iridovirus in large yellow croaker by PCR

A rapid and sensitive PCR-based method for the detection of the large yellow croaker iridovirus(LYCIV) is described,which involves the amplification of a 295 bp fragment of the LYCIV ATPase gene from DNA isolated from naturally infected fish spleen.Sequencing of LYCIV ATPase gene fragment showed it shared 100% nucleotide sequence homology with the corresponding region of the ATPase gene of red sea bream iridovirus(RSIV) and sea bass iridovirus(SBIV),suggesting that LYCIV was homologous with RSIV and SBIV at least in part of the gemone.The specificity and sensitivity of the PCR procedure were tested on the iridovirus-infected fishes,the expected fragment was detected from spleen DNA samples of infected fishes,whereas no fragments were amplified from healthy fish spleen DNA,white spot syndrome baculoviruses(WSBV) DNA and pseudorabies virus(PRV) DNA.Detection limit of this method was 10^-7 ng positive plasmid DNA containing target sequence,equal to about 100 virions.In the infected experiment,first positive detection(1/4) appeared at Day 3 post-infection,all fish(4/4) tested positive at Day 7,however obvious symptoms were observed at Day 8,so LYCIV infection could be detected prior to the appearance of obvious symptoms.These results indicate that this PCR method could be used for early,rapid and specific detection of LYCIV infection.     

水产饲料膨化机设计刍论

据开发应用水产饲料膨化机实践，初步论述了膨化机生产能力与动力匹配，螺杆设计参数长径比，物料在腔内滞留时间，膨化腔设计及其温度调控，并提出改进设计的见解.     

Rapid detection of virulent protease secreted by Vibrio anguillarum by dot enzyme-linked immunosorbent assay

Dot enzyme-linked immunosorbent assay （dot-ELISA）, indirect ELISA and Westem blot were performed to detect the virulent protease secreted by Vibrio anguillarum which was isolated from the diseased left-eyed flounder, Paralichthys olivaceous. Sensitivity results showed that dot-ELISA is a more sensitive, rapid and simple technique for the protease detection. The minimal detectable amount of protease is about 7 pg in the dot-ELISA test, while 7.8 ng in the indirect ELISA and 6.25 ng in the Westem blot respectively. Protease could be detected 2 h after incubation of V. anguillarum in the 2216E liquid medium but enzyme activity was very low at that period. From 6 to 12 h, the amount and enzyme activity of protease increased markedly and reached maximum at stationary phase. Analysis of serum samples periodically collected from the infected flounders showed that after 2 h of infection by V. anguillarum, the pathogenic bacteria could be detected in the blood of the infected flounders but no protease was found. It was 5-6 h after infection that the protease was detected in blood and then the amount increased as infection advanced. Quantitative detection of protease either incubation in the medium or from the blood of infected flounders could be accomplished in virtue of positive controls of quantificational protease standards （＂marker＂） so that the alterations ofprotease secretion both in vitro and in vivo could be understood generally. In addition, the indirect ELISA and dot-ELISA were also performed to detect V. anguillarum cells. Results indicated that the sensitivity of indirect ELISA to bacteria cells is higher than that of the dot-ELISA, and that the minimal detectable amount is approximately 10^4 cell/mL in the indirect ELISA, while 10^5 cell/mL in the dot-ELISA.