顶空固相微萃取气相色谱质谱嗅觉测量联用初探鲢肉的挥发性风味物质

为探明鲢肉挥发性气味特征物质,通过顶空固相微萃取法提取和浓缩了鲢肉中的挥发性物质,并利用气相色谱质谱联用以及气相色谱〖CD*7/9〗嗅觉测量法对气味物质进行了定性分析及气味特征的评价。由8人组成的评价小组通过检测频率法进行嗅觉测量。结果表明,经GCMS分析鉴定得到了29种挥发性气味物质,主要是一些羰基类和醇类化合物,占了总挥发性物质的88%。通过检测频率分析法鉴定出12种化合物具有气味特征,表现为鱼腥、金属、青草、油脂氧化、蘑菇等特征。另外有4种未知物也显示了较强的风味特性,它们协同作用构成了鲢的特殊气味。     

Pectin purified from pomelo (Citrus maxima) peel as a natural hatching agent for fish embryos

Pectin is a biodegradable polysaccharide, and it has been recently applied as a gene delivery, drug delivery, wound healing and tissue engineering agent. In this study, pectin was extracted from pomelo (Citrus maxima) peel and characterized. The extraction recovery of pectin form pomelo peel was 14.5%, and it had 72.56% degree of esterification, 1,245.56 equivalent weight, 7.82% methoxyl and 68.27% anhydrouronic acid contents. Use of pomelo pectin as a hatching enhancing agent for fish embryos and its effect on hatching enzyme 1 (ZHE1) was investigated. The pectin‐exposed zebrafish embryos (100 µg/ml) showed significantly (p < .05) higher hatching rate (96.6%) compared with untreated (control) embryos (66.6%) at 60 hpf. The mRNA expression of ZHE1 was also significantly (p < .05) elevated up to 55.6‐fold in pectin‐exposed embryos at 24 hpf. In situ hybridization results revealed remarkably strong expression of ZHE1 in pectin‐exposed embryos compared with the control group. In addition, considerably larger size of the hatching gland was observed in pectin‐exposed larvae than that of the unexposed larvae group. These results clearly indicate that pectin isolated from pomelo peel has an ability to enhance the hatching process of zebrafish embryos via upregulation of ZHE1.     

倒刺鲃的胚胎发育及水温对胚胎发育的影响

对倒刺鲃的胚胎发育进行连续跟踪观察,并探讨了水温对其胚胎发育的影响。结果表明:水温(25±0.5)℃时,孵化时间为53.43 h;胚胎发育过程中出现克氏囊。水温21～33℃条件下,倒刺鲃的胚胎均能孵化,水温(x)与孵化时间(y)成极显著的负相关关系:y=235.72 e-0.056 6x,P<0.01;水温与积温的关系为:y=7 519.4x-0.519 2,P<0.01。孵化率(y)与水温(x)相关关系式为:y=-1.665 5x2+88.621x-1 091.5,由曲线方程可以推算出胚胎发育的适宜水温范围为23.4～29.8℃,通过曲线求导数推算极值的方法,求得胚胎发育的最适水温为26.6℃。     

上海市水产品比较优势研究

改革开放以来，上海渔业经济的发展取得了巨大成就，但上海也为此付出了巨大代价：一是许多宝贵的水产资源逐渐衰竭；二是水产养殖导致了环境污染。上海如果要实现渔业的可持续发展，就必须注意搞好渔业产业结构的布局，发展自己的比较优势产业。文章针对如何确定上海渔业比较优势的问题详细介绍了用国内资源成本测定水产品比较优势的方法，并运用该方法测算了上海主要水产品的比较优势，旨在为上海市渔业生产结构的调整提供一定的参考和依据。     

Regeneration of adventitious shoots from mature stored cotyledons of Japanese plum (Prunus salicina Lind1)

Adventitious shoot regeneration from mature stored cotyledons of Japanese plum (Prunus salicina Lind1) was achieved in vitro. The influences of the presence and absence of the light, different concentrations of thidiazuron (TDZ) and benzyladenine (BA) in the culture media, TDZ pretreatments and different basal salts on shoot regeneration were evaluated. TDZ was more effective in inducing shoot regeneration from mature stored cotyledons than BA. Dark incubation significantly increased the regeneration frequencies. Quoirin/Lepoivre (QL) basal salts stimulated shoot regeneration more than woody plant (WPM) or B5 salts did. The frequency of adventitious shoot formation varied among the varieties and the regeneration ability appeared to be genotype depended. The frequency of regeneration under the optimum tested conditions for ‘Bruce’, ‘Shiro’, ‘Redheart’, ‘Gladstone’ and ‘Early Golden’ cotyledons were 66.7%, 46.7%, 43.3%, 26.7% and 6.7%, respectively.     

Genetic analysis of Aequipecten opercularis and Mimachlamys varia (Bivalvia: Pectinidae) in several Atlantic and Mediterranean localities, revealed by mitochondrial PCR-RFLPs: a preliminary study

Aequipecten opercularis (Queen scallop) and Mimachlamys (Chlamys) varia (Black scallop) are important natural resources occurring in Atlantic and Mediterranean coasts. To develop an optimal sustainable exploitation plan, it is important to study the genetic structure of the different populations. In this study, we used polymerase chain reaction‐restriction fragment length polymorphisms for the determination of the genetic variation and population structure of these two species in different localities. Ten composite haplotypes were generated for A. opercularis and 15 haplotypes for M. varia. Of these, six and four were unique respectively. The analysis of the distribution of the different haplotypes between the localities showed no clear evidence of subdivision in A. opercularis, while in M. varia the results indicated that the two localities analysed should be managed as separate stocks.     

Effects of stocking density on haematological parameters,growth and fin erosion of great sturgeon (Huso huso) juveniles

The influence of stocking density (1, 2, 4, 6 and 8 kg m^?2) was investigated on haematological parameters, growth and fin erosion of great sturgeon (Huso huso) juveniles for a period of 8 weeks. The mean weight of fish at the start of trial was 93.13±1.04 g. After 8 weeks of rearing, the mean weight was 362.4, 319.7, 267, 242.1 and 211.1 in densities 1–8 kg m^?2 respectively. The results of this study showed that growth parameters, including condition factor, weight, weight gain, feed conversion ratio, specific growth rate and body weight increase, had a statistically significant difference among treatments (P<0.05). A significant difference (P<0.05) was observed in haematocrit, but the other haematological parameters, including red blood cells, white blood cells (WBC), haemoglobin concentration, mean corpuscular haemoglobin, mean corpuscular volume, mean corpuscular haemoglobin concentration and differential WBC count, showed no significant effect with stocking density (P>0.05). At the end of the experiment, stocking density had no significant effect on plasma cortisol and glucose concentration. The fin length (dorsal, anal, ventral, pectoral and caudal) of fish was measured to calculate the fin index. According to this index, dorsal, anal, ventral and pectoral fins showed no significant difference among treatments (P>0.05), but the erosion of the caudal fin was significantly different between fish held on 6 and 8 kg m^?2 (P<0.05). These results showed that rearing density has a major effect on the growth indices of H. huso. Unlike many other fish, great sturgeon exhibited lower stress responses to high stocking density. This indicates that they are more tolerable to rearing conditions in high stocking densities. With respect to the various effects that density causes on growth, fin erosion and physiological and haematological parameters, better understanding of these phenomena considering different levels of density could have a beneficial impact on many rearing steps of this species.     

利用SRAP分子标记技术鉴定大白菜种子纯度

以大白菜品种多抗3及其父母本为研究材料,利用SRAP（相关序列扩增多态性）分子标记方法,通过对54对SRAP标准引物的筛选,获得了能区分大白菜多抗3及其亲本的引物Me4F/Em3R。采Me4F/Em3R引物对对5份多抗3系列商品种子纯度进行检验,种子的纯度分别为75.5%、72%、80.5%、68%和73%,与田间种植纯度鉴定结果符合率分别为94.6%、89.3%、93.2%、95.5%和91.25%。说明利用SRAP分子标记方法对多抗3大白菜一代杂种进行快速、准确的纯度鉴定是可行的。     

西南地区普通小麦1BL/1RS易位系的DArT分子标记鉴定

为了准确了解小麦品系中1BL/1RS易位系的存在,利用7 000多个DArT分子标记(Diversityarrays technology,多样性微阵列技术)对87个普通小麦品系进行扫描,总共获得1 750个稳定的多样性的分子标记(P>80)。这些标记的多态性信息含量指数(PIC)的范围是0.03～0.5,平均值为0.35(P>80)。根据DArT标记的可整合性,利用1B染色体上的DArT数据进行主坐标分析(Principal-Coordinates Analysis,PCoA),可以把实验材料划分为两个群,并且确定一个群是由1BL/1RS易位系组成,另一个群由非1BL/1RS易位系组成。同时,利用非加权组平均法(Unweighted pair-group method with arithmetic means,UPGMA)进行聚类分析,调查了材料之间的遗传关系,结果显示,实验材料同样聚集为两个群,一个群由1BL/1RS易位系组成,包含两个亚群;另一个群由非易位系组成,包含六个亚群。研究证实,DArT标记不仅可以调查小麦全基因组的遗传多样性,而且利用它的可整合性能够准确鉴定研究材料中的1BL/1RS易位系。     

Development and application of fluorescence in situ hybridization (FISH) method for simple and rapid identification of the toxic dinoflagellates Alexandrium tamarense and Alexandrium catenella in cultured and natural seawater

ABSTRACT:   The toxic dinoflagellates Alexandrium tamarense (Lebour) Balech and A. catenella (Whedon and Kofoid) Balech produce potent neurotoxins, such as saxitoxin and gonyautoxin and have been mainly responsible for paralytic shellfish poisoning (PSP) in Japan. To prevent a negative effect on the fishery industry, it is necessary to identify these toxic species precisely and rapidly before and during the bloom. In this paper, a rapid and simple protocol of a fluorescence in situ hybridization (FISH) method using ribosomal RNA (rRNA)-targeted probes has been established for identifying the cultured strains and natural cells of A. tamarense and A. catenella . Using the FISH method established in this study, it was possible to identify these toxic species species-specifically and rapidly, within 30 min. The procedure of detection constituted three steps: (i) fixation/dehydration; (ii) hybridization; and (iii) washing; this made the identification simple. Moreover, this method did not require either special techniques or equipment, and the cost for detection was low. The specificity, rapidity, and simplicity of the developed method suggest that it might be useful for routine monitoring of these toxic microalgae.