紫贻贝与厚壳贻贝杂交子代生长和存活比较

利用辽宁大连的紫贻贝(Mytilus galloprovincialis)与福建宁德的厚壳贻贝(M.coruscus)为亲本,采用2×2双列杂交设计,构建了紫贻贝自交组(M.galloprovincialis♀×M.galloprovincialis♂)、正交组(M.galloprovincialis♀×M.coruscus♂)、反交组(M.coruscus♀×M.galloprovincialis♂)与厚壳贻贝自交组(M.coruscus♀×M.coruscus♂)4个遗传组合,比较分析了受精率、孵化率、子代的成活率、生长数据等,探讨了紫贻贝与厚壳贻贝种间杂交的可行性,同时为贻贝良种选育提供参考。结果表明,自交组与反交组的受精强度具有不对称性,正交组与自交组受精率无差异,反交组的受精率及孵化率显著低于正交组与自交组(P0.05),且浮游幼虫不能正常存活;正交组子代具有生长优势,第9、11、13天的浮游幼虫及第78天的稚贝壳长均显著大于自交组(P0.05);正交组与紫贻贝自交组在整个幼虫阶段存活率无显著差异,在壳顶幼虫期显著高于厚壳贻贝自交组(P0.05)。     

三种典型POPs对紫贻贝不同组织DNA损伤的比较研究

采用彗星电泳技术,比较研究了Aroclor 1254、BaP、DDT三种典型POPs对紫贻贝(Mytilus edulis)鳃、性腺、消化腺细胞的DNA损伤效应的差异,以期为进一步评价这三种典型POPs遗传毒理机制及其预警监测提供科学依据.结果表明,Tail DNA%是评价DNA损伤的理想指标,另外,在急性毒性试验中,...     

若干生态因子对缢蛏稚贝生长和存活的影响

本文系在实验室条件下,研究用不同的饵料密度、稚贝密度、光照强度、底质以及这些因子相结合对缢蛏稚贝生长和存活的影响,从中找出缢蛏育苗的最佳培养条件,为人工或半人工育苗提供参考。     

低盐度形成的微生物膜对厚壳贻贝稚贝附着的影响

为研究环境因子在厚壳贻贝(Mytilus coruscus)稚贝附着过程中的调控作用, 作者探讨了低盐度对微生物膜生物构成、群落结构的影响及所形成微生物膜对厚壳贻贝稚贝附着的影响。在实验室条件下, 研究微生物膜的日龄与干质量、细菌密度和硅藻密度、叶绿素a含量的关系及其对厚壳贻贝稚贝附着的影响。通过DGGE指纹图谱技术对微生物膜中的细菌群落结构多样性进行了分析。研究发现,盐度13和23时形成的微生物膜能有效促进厚壳贻贝稚贝的附着, 且盐度23、28d时稚贝附着率最高, 达到72%。相关性分析表明, 微生物膜的诱导活性与盐度、干质量、细菌密度、硅藻密度、日龄呈显著正相关性, 与叶绿素a无相关性。微生物膜的干质量、附着细菌密度及底栖硅藻密度明显随着日龄的增加而增加, 叶绿素a含量与微生物膜日龄无显著相关性。细菌群落在厚壳贻贝稚贝附着过程中发挥重要调控作用。     

不同保存方法对厚壳贻贝样品蛋白提取效果的比较

为了解厚壳贻贝(Mytilus coruscus)稚贝样品在冷冻保存过程中的蛋白变化情况,作者采用直接冷冻法、添加海水冷冻法、蛋白裂解液冷冻法等分别对保存1周至6个月的厚壳贻贝样品蛋白提取的不同效果进行了比较。SDS-PAGE胶结果显示,3种冷冻保存方法均出现4个有规律条带(a、b、c、d),其相对分子量依次约为55、46、38和26kDa。SDS-PAGE蛋白条带灰度值的检测结果表明,1个月内蛋白裂解液法保存的样品最佳;直接冷冻法和添加海水冷冻法的研究发现保存过程中的蛋白均出现不同程度的降解现象,因而可能不适宜用于该种稚贝样品的保存。     

环境因子对小刀蛏稚贝生长和存活的影响

采用单因子分析方法,以小刀蛏为材料,研究了不同盐度、温度、底质及饵料对小刀蛏稚贝生长和存活的影响。实验结果表明:小刀蛏稚贝具有较强的盐度耐受性,可以在较大的盐度变动范围内生长和存活;小刀蛏稚贝生长和存活的适宜盐度范围为15~35,最适盐度范围为20~25;适宜的温度范围为16~28℃,最适的温度范围为24~28℃;随着盐度和温度的增加,小刀蛏稚贝的生长率和存活率均呈先升高后降低的变化趋势。底质是小刀蛏生长和存活的必要环境条件,且小刀蛏对底质环境具有明显的选择性,稚贝以海泥底质最佳,实验条件下海泥底质组生长率和存活率显著高于半泥半砂底质和细粉砂底质。不同饵料对稚贝的培育效果不同,角毛藻和金藻的投喂效果最好,稚贝生长率和存活率最高,其次为扁藻组,小球藻组最差。研究结果可为小刀蛏人工培育技术的优化提供参考依据。     

肠道细菌对厚壳贻贝稚贝附着的作用研究

为探讨肠道细菌形成的微生物被膜对贝类附着的作用,从厚壳贻贝(Mytilus coruscus)成体肠道中分离10株肠道细菌,调查厚壳贻贝肠道细菌形成微生物被膜特性,分析微生物被膜密度、细菌种属与厚壳贻贝稚贝附着之间的相互关系。所有肠道细菌均可有效促进稚贝附着。其中,Paracoccus sp.1微生物被膜诱导的稚贝附着率最高(61%),且微生物被膜膜厚较厚,细菌分布较密集;仅5株肠道细菌Roseovarius sp.1、Winogradskyella sp.1、Tenacibaculum sp.4、Bacillus sp.5和Nonlabens sp.1的被膜密度与附着显著相关(P0.05)。系统发育分析发现肠道细菌诱导附着率与其种属无关。本研究表明源于厚壳贻贝成贝肠道细菌可以促进其稚贝的附着,说明肠道细菌对厚壳贻贝的生长发育具有一定的作用。本研究结果为深入探讨肠道细菌与厚壳贻贝相互作用和推动该种规模化养殖提供理论依据。     

紫贻贝养殖产业的现状、问题与对策

为全面系统地了解中国紫贻贝(Mytilus galloprovincialis)养殖产业情况,作者从养殖产量、养殖面积、进出口贸易、养殖生产等方面概述了紫贻贝产业现状,对中国紫贻贝养殖业的种质资源、苗种生产方式、养殖生产流程、养殖方式等进行了综述,并针对紫贻贝养殖中存在的问题,从种质资源、养殖模式、设施设备、食品安全控...     

几种环境因子对墨西哥湾扇贝幼虫和稚贝生长与存活的影响

叙述了在室内控制条件下海水温度、盐度和pH因子对墨西哥湾扇贝Argopecten irrndians concentricus浮游幼虫和稚贝生长和存活的影响。结果表明，墨西哥湾扇贝浮游幼虫生长的适宜温度为20-30℃，最佳生长温度为25-30℃。稚贝生长的适宜温度为15-33℃，最适生长温度为25-30℃。浮游幼虫生长的适宜盐度为23．38-42．70，最适生长盐度为23．38-36．58；稚贝生长的适宜盐度为23．38-42．70，最适生长盐度为23．38-36．58；在pH为7-8时，稚贝存活率最高，生长最好。稚贝的耐干露能力低下。     

管角螺Hemifusus tuba(Gmelin)稚贝在不同盐度下的生长和存活研究

在水温28.6—29.5℃、pH8.2条件下,研究了管角螺Hemifusus tuba稚贝[(壳高19.5±1.23)mm、体重(661.4±48.6)mg]在不同盐度下的生长和存活,并用二点法计算出最适宜存活和生长的盐度范围。结果表明,管角螺稚贝适宜存活盐度和最适存活盐度分别为17.7‰—40.8‰和25.1‰—35.9‰,适宜生长盐度和最适生长盐度分别为17.5‰—39.9‰和27.8‰—33.2‰。在最适生长盐度范围内,稚贝壳高日平均增长率为0.358—0.397mm.d 1,体重日平均增长率为44.64—49.09mg.d 1。超出上述范围,其存活率下降、生长率降低。稚贝在盐度17.0‰和41.3‰的海水中适应20d后再分别移至盐度14.0‰和45.0‰的海水中,72 h后存活率分别为84.0%和96.0%,而直接把生活在盐度为30.5‰中的稚贝放入到盐度为14.0‰和45.0‰的海水,72h后其存活率为8.0%和0,可见稚贝对盐度的适应能力与原生活海水盐度有关,经过驯化后的稚贝能够扩大对盐度的适应范围,提高对盐度的耐受力。     

Effects of 17β-estradiol exposure in the mussel Mytilus galloprovincialis

Mussels Mytilus galloprovincialis were exposed to different concentrations of estradiol (20, 200, and 2000 ng/l) in a semi-static regime (1-day dosing intervals) for up to 7 days in an attempt to see how mussels dealt with exogenous estrogenic compounds. Sex hormone levels were determined in whole tissue. Free-estradiol was only significantly elevated at the highest exposure dose (up to 10-fold). Most of the estradiol was in the tissues as fatty acid esters (>78%), which sharply increased in a dose-dependent manner (from 4 ng/g in controls to 258 ng/g at the high exposure group). In contrast, neither free nor esterified testosterone levels showed significant differences between control and exposure groups. The results suggest the existence of mechanisms that allow mussels to maintain their hormonal status, and the important role that fatty acid esterification may play within those mechanisms. Synthesis and conjugation rates of estradiol were further investigated by measuring the activity of P450 aromatase, and palmitoyl-CoA:estradiol acyltransferase, in digestive gland microsomal fractions. Overall, the study contributes to the better knowledge of molluscan endocrinology, and defines new mechanisms of regulation of free steroid-levels in mussels.     

花生四烯酸调控网络在贻贝麻痹性贝毒代谢中的作用基于转录组和代谢组联合分析

紫贻贝（Mytilus galloprovincialis）是富集麻痹性贝类毒素（Paralytic Shellfish Toxins, PSTs）能力很强的代表性双壳贝类,但研究表明紫贻贝暴露于PSTs也会引起机体炎症反应,其作用机理及对毒素代谢影响尚不清楚。本研究采用转录组学与代谢组学联合分析技术,比较了产PSTs的链状亚历山大藻（Alexandrium catenella）暴发的不同时期,紫贻贝机体的基因表达量与代谢物含量差异,以解析PSTs胁迫下紫贻贝机体的炎症反应机制。结果表明,紫贻贝暴露于PSTs后表达的基因和代谢物均发生显著变化,其中差异表达基因17232个,差异代谢物341个。基于联合分析,差异表达基因与差异代谢物显著富集在花生四烯酸和谷胱甘肽代谢通路中,基因PLA2G2F、ALOX5、TBXAS1以及代谢物ARA、PGH₂、TXA₂、LTA₄、5-HETE对贻贝机体的促炎反应发挥重要作用;而基因GPX4、CYP2J2和代谢物15-HETE、GSH则调节机体炎症的消退。本研究揭示花生四烯酸相关通路在贻贝机体炎症反应过程中具有重要的调控作用,为下一步深度揭示PSTs胁迫下贻贝机体炎症网络化响应机制提供了研究基础。     

紫贻贝体尺性状和体质量性状对足丝性状的影响分析

为研究紫贻贝(Mytilus galloprovincialis)体尺性状和体质量性状对足丝性状的影响,作者选取山东省青岛市即墨养殖区的紫贻贝为研究对象,分别测量壳长、壳宽、壳高等3个体尺性状,全湿质量、软体质量2个体质量性状以及足丝直径和足丝茎直径2个足丝性状,通过相关性分析、多元回归分析和通径分析等方法分别研究了体尺性状和体质量性状对足丝性状的影响。结果显示:所有性状间相关系数为0.678～0.892,性状间相关性达到极显著水平(P<0.01);多元回归和通径分析结果显示,壳高和全湿质量分别对足丝性状的影响最大,壳高对足丝性状通径系数分别为0.515和0.508,全湿质量对足丝性状分别为0.417和0.520;建立了体尺性状、体质量性状对足丝直径和足丝茎直径的回归方程。     

Spatial and temporal variation of biomarkers in mussels (Mytilus galloprovincialis) from the Lagoon of Venice, Italy

A multiple biomarker approach was adopted in a seasonal study carried out in the Lagoon of Venice, with the double aim of evaluating the natural and anthropic stresses influencing the biological responses of mussel (Mytilus galloprovincialis) and of assessing the effects due to spatial rather than temporal variations.Biochemical (aldehyde dehydrogenase and catalase activities), cellular (neutral red retention time) and physiological (survival in air and condition index) biomarkers were determined in mussels collected in four differently impacted lagoon areas.Multivariate analysis showed that samples were distributed mainly according to temperature and four seasonal groups were identified. The combination of spatial and temporal information enabled us to distinguish physiological variations due to natural causes from those due to anthropic stress, and to identify the sampling period when several biomarkers are less influenced by both natural and endogenous factors.     

基于CO1基因的渔山列岛厚壳贻贝遗传资源评估

基于线粒体CO1基因的序列,对渔山列岛,大连獐子岛,南麂列岛,山东南隍城乡,舟山嵊泗5个野生群体的厚壳贻贝进行遗传多样性和遗传结构的分析。结果表明:在mt DNACO1基因同源片段上共检测到了39个多态位点,其中39个简约信息位点,无单突变位点,构成40个单倍型,群体遗传多样性水平为:渔山山东大连舟山南麂;然而单倍型多样性却是山东渔山南麂大连舟山。分子进化树和单倍型网络关系图构建结果显示:5个群体之间分为3个单倍型类群(A、B、C),其中A类群含15个单倍型,B类群含23个单倍型,C类群含2个单倍型(均为渔山列岛的单倍型),其中渔山列岛的单倍型在上述三个类群中都有分布。3个单倍型类群间的遗传距离为0.0099~0.0268。渔山列岛群体内遗传分化较为显著,其他4个群体间未检测到显著的遗传分化。     

CYP1A- and CYP3A-immunopositive protein levels in digestive gland of the mussel Mytilus galloprovincialis from the Mediterranean Sea

CYP1A-immunopositive protein can be elevated in response to planar PAHs and PCBs in Mytilus sp. digestive gland whilst CYP3A-immunopositive protein has been associated with testosterone 6β-hydroxylation in fish. Levels of CYP1A- and CYP3A-immunopositive protein were determined in Mytilus galloprovincialis digestive gland microsomes collected from 12 sites in the Mediterranean Sea during May and September 2001. CYP1A-immunopositive protein was significantly highest at contaminated sites whilst CYP3A-immunopositive protein was significantly lowest. A weak negative correlation (r²=0.21) was seen between CYP1A- and CYP3A-immunopositive protein. Little evidence of differences at the different sampling times was observed. These results confirm previous work indicating elevation of CYP1A-immunopositive protein in Mytilus sp. digestive gland at contaminated sites. Further study is required to characterise CYP3A-like expression in Mytilus and to elucidate the consequences of possible CYP3A-like down-regulation at contaminated sites.