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1.
模拟吹填、疏浚等海上施工过程所产生的底泥悬浮物浓度的变化规律,探讨不同底泥悬浮物浓度下对凡纳滨对虾仔虾成活影响。结果表明:海水中底泥悬浮物浓度超过10mg/L,持续时间超过12h时,将对凡纳滨对虾成活率产生影响,随着悬浮物实验浓度的递加,仔虾的死亡率从13.33%增至96.67%;超过80mg/L,且持续时间超过48h,将对凡纳滨对虾产生严重影响,甚至导致全部仔虾的死亡;悬浮物对凡纳滨对虾的12h、24h、36h和48h半致死量(LC50)分别为54.56、40.29、25.8和19.18mg/L。  相似文献   

2.
眼柄粗提物对凡纳滨对虾性分化的影响   总被引:1,自引:0,他引:1  
采用生化方法制备凡纳滨对虾[Litopenaeus(Penaeus)vannamei)]眼柄粗提物,用活体注射法研究不同粗提物剂量对去眼柄凡纳滨对虾卵母细胞直径大小的影响,以检验其性腺抑制素(Gonadinhibiting hormone,GIH)的生物活性;在凡纳滨对虾仔虾后17、22和27 d,分别以不同浓度眼柄粗提物浸泡24 h,结果显示:除0.001个眼柄/mL的GIH浓度外,0.01、0.1和1个眼柄/mL组均显著降低凡纳滨对虾卵母细胞直径(P﹤0.05);浸泡处理后,仔虾后17 d GIH处理组凡纳滨对虾雌性率达70.1%~80.1%;仔虾后22 d GIH处理组雌性率达65.8%~71.7%,各浓度GIH处理组雌性率比对照组(雌雄比例约为1:1)显著提高(P﹤0.05);仔虾后27 d,0.01和1个眼柄/mL处理组雌性率(约58%)略高于对照组,但0.1个眼柄/mL处理组雌性率(73.1%)与对照组相比显著提高(P﹤0.05)。结果表明较低浓度的眼柄粗提物可明显诱导凡纳滨对虾雌性化,在仔虾后22 d前处理效果最佳。  相似文献   

3.
通过显微观察和组织学连续切片,对凡纳滨对虾的促雄性腺进行研究。结果表明:凡纳滨对虾的促雄性腺埋于精荚囊端壶腹外侧的肌肉中,呈不规则的块状,Harris苏木精染色呈嗜碱性。H?E染色显示,促雄性腺主要由两种形态的细胞构成,一种核质致密嗜碱性非常强,细胞核被染成深蓝色,核仁很难辨认,大多呈圆形或卵圆形(A型细胞);另一种细胞多为卵圆形,细胞核较大,核质疏松,被染成浅蓝色,核仁1~2个清晰可见(B型细胞)。此外,促雄性腺中A、B细胞的出现及其数量随精巢发育而发生变化,繁殖完成后细胞解体。  相似文献   

4.
虾类微量元素含量的主成分分析   总被引:2,自引:0,他引:2  
应用主成分分析法对湛江几种养殖对虾和海捕天然对虾的微量元素的含量进行综合评价。结果表明:虾体中微量元素含量均衡;综合排名依次为野生斑节对虾、野生凡纳滨对虾、养殖斑节对虾、养殖凡纳滨对虾,两种野生对虾的综合排名均高于养殖对虾;野生斑节对虾综合得分为1.6708,微量元素含量最均衡,营养价值最高,养殖凡纳滨对虾营养价值最低,综合得分为-1.20943。  相似文献   

5.
植酸酶对凡纳滨对虾生长性能和体成分的影响   总被引:1,自引:0,他引:1  
在凡纳滨对虾饲料中添加不同量微生物植酸酶(0,500,1000,2000 U/kg),观察虾的存活率、增重率、饲料系数及虾体和虾壳成分,研究饲料中添加植酸酶对凡纳滨对虾生长性能的影响。结果表明:饲养8周后,饲料中添加500~2000 U/kg植酸酶对凡纳滨对虾增重率、存活率和饲料利用无显著影响(P>0.05);植酸酶添加各组与对照组虾体的水分、粗蛋白、脂肪、灰分、总钙和总磷含量差异不显著;虾壳中粗灰分和钙含量在500和1000 U/kg组显著高于对照组和2000 U/kg组(P<0.05),虾壳磷含量在各饲料组间差异不显著。血清磷浓度在对照组和2000 U/kg组显著高于500 U/kg组(P<0.05),血清钙浓度在组间差异不显著,血清碱性磷酸酶活性以对照组最高,显著高于500和1000 U/kg组。结果说明,在特定试验条件下,饲料中添加植酸酶对凡纳滨对虾幼虾的虾壳和血清成分有显著影响(P<0.05),对幼虾生长性能影响不显著(P>0.05)。  相似文献   

6.
【目的】建立快速检测凡纳滨对虾野田村病毒的RT-PCR方法。【方法】根据GenBank中获得的凡纳滨对虾野田村病毒的基因序列,应用Oligo6.0软件设计合成1对特异性扩增引物,对反应条件和反应体系进行优化,建立快速检测凡纳滨对虾野田村病毒的RT-PCR方法。用该方法对感染野田村病毒的凡纳滨对虾进行RT-PCR检测。【结果】RT-PCR可扩增出与设计相符的413 bp的特异性目的条带,而对白斑症病毒(WSSV)阳性虾、对虾杆状病毒(BP)阳性虾、传染性皮下及造血器官坏死病毒(IHHNV)阳性虾、肝胰腺细小病毒(HPV)阳性虾、黄头病毒(YHV)阳性虾、传染性肌肉坏死病毒(IMNV)阳性虾、桃拉病毒(TSV)阳性虾和健康虾的扩增结果均为阴性。测序比对结果表明,该方法检测结果准确,最低可检测出约100 fg/mL的野田村病毒重组质粒DNA;用该方法对从福建、广东、海南、广西、江苏、浙江、山东等地的386份临床样品进行RT-PCR检测,共检出野田村病毒阳性样品64份。【结论】该方法可用于凡纳滨对虾野田村病毒的快速检测。  相似文献   

7.
【目的】研究凡纳滨对虾(Litopenaeus vannamei)miRNA-184 [microRNA-184(miR-184),记作LvmiR-184]在健康虾及染病虾中的表达,探讨其免疫功能。【方法】用茎环法克隆鉴定凡纳滨对虾LvmiR-184,通过荧光定量PCR检测LvmiR-184在对虾血淋巴、肝胰腺、鳃、肌肉、心脏、胃、肠和眼柄等8个组织中的分布。对凡纳滨对虾注射副溶血弧菌(Vibrio parahaemolyticus),检测LvmiR-184不同时间点的响应变化。对感染副溶血弧菌的凡纳滨对虾分别注射0.3、3.0和30.0 ng的mi R-184模拟物和抑制物,检测不同时间点对虾血细胞凋亡率。【结果与结论】LvmiR-184在所有组织中均有表达,在胃中表达量最高,其次是肌肉,鳃表达量最低。注射副溶血弧菌后1.5 h,LvmiR-184表达量显著上调;在24 h达到峰值,较对照组高8.25倍;对照组则维持在较低的水平。模拟物、抑制物注射量为30 ng时对虾血细胞凋亡率差异有统计学意义(P 0.05);与对照组凋亡率相比,注射模拟物6 h后提高62%。LvmiR-184可调控凡纳滨对虾的血细胞凋亡。  相似文献   

8.
在凡纳滨对虾饲料中添加不同量微生物植酸酶(0,500,1000,2000U/k),观察虾的存活率、增重率、饲料系数及虾体和虾壳成分,研究饲料中添加植酸酶对凡纳滨对虾生长性能的影响。结果表明:饲养8周后,饲料中添加500-2000U/kg植酸酶对凡纳滨对虾增重率、存活率和饲料利用元显著影响(P〉0.05);植酸酶添加各组与对照组虾体的水分、粗蛋白、脂肪、灰分、总钙和总磷含量差异不显著;虾壳中粗灰分和钙含量在500和1000U/k组显著高于对照组和2000U/kg组(P〈0.05),虾壳磷含量在各饲料组间差异不显著。血清磷浓度在对照组和2000U/kg组显著高于500U/kg组(P〈0.05),血清钙浓度在组间差异不显著,血清碱性磷酸酶活性以对照组最高,显著高于500和1000U/kg组。结果说明,在特定试验条件下,饲料中添加植酸酶对凡纳滨对虾幼虾的虾壳和血清成分有显著影响(P〈0.05),对幼虾生长性能影响不显著(P〉0.05)。  相似文献   

9.
抗菌肽对凡纳滨对虾生长和机体免疫的影响   总被引:1,自引:0,他引:1  
基础饲料(对照组)中添加10g/kg抗菌肽制剂喂养体重0.10±0.01g、体长2.17±0.11cm的凡纳滨对虾(Penaeus vannamei)30d,进行10d的水浴攻毒(鳗弧菌10~8/mL),探讨饲料中添加抗菌肽对凡纳滨虾生长、成活率、免疫保护率,以及肌肉中溶菌酶活性、超氧化物歧化酶活性、总抗氧化能力的影响。结果表明:饲料中添加抗菌肽可显著提高凡纳滨对虾相对增重率、成活率和对致病菌的免疫保护率(P<0.05),但对饲料系数无显著影响(P>0.05);未受外界微生物刺激时,饲料中添加抗菌肽对凡纳滨对虾总抗氧化能力有促进作用(P<0.05),受外界微生物刺激后,饲料中添加抗菌肽喂养凡纳滨对虾可提高对虾超氧化物歧化酶活性(P<0.05)和总抗氧化能力(P<0.01)。因此饲料中添加抗菌肽喂养凡纳滨对虾可提高其机体非特异性免疫。  相似文献   

10.
在凡纳滨对虾饲料中分别添加大黄0、0.5、1.0、5.0、10.0和20.0g/kg,研究大黄对凡纳滨对虾(初始体重为0.34±0.004g)生长及非特异性免疫指标的影响。结果表明,大黄对凡纳滨对虾成活率、增重率、特定生长率、饲料系数、蛋白质效率和蛋白质累积率的影响不显著(P>0.05),对全虾和尾肌肉的灰分、脂肪和粗蛋白含量影响显著,全虾的粗蛋白和粗脂肪含量以1.0g/kg组最高(P<0.05),对凡纳滨对虾血清碱性磷酸酶、酸性磷酸酶、酚氧化酶、超氧化物歧化酶、溶菌酶以及血清总蛋白量等的影响显著,溶菌酶活性以1.0g/kg组最高(P<0.05);细菌感染实验中以1.0g/kg组存活率最高(P<0.05)。以非特异性免疫反应指标及感染实验存活率为指标,凡纳滨对虾饲料中大黄的适宜添加量为1.0g/kg。  相似文献   

11.
Epidermal cells of amphioxus at different developmental stages were investigated by electron microscopy and colloidal carbon tracing experiments. Amphioxus epidermal cells showed different ultrastructural characteristics at larval and adult stages. The epidermal cells at all larval stages studied (24–96 h) had numerous vesicles containing electron dense materials in their apical cytoplasm. In tracing experiments, carbon particles were found in apical vesicles and interoellular spaces. Under scanning electron microscope, many crater-like protrusions were observed on the surface of the cells. These results indicated that amphioxus larval epidermal cells may be capable of endocytosis. The epidermal cells of 3-month and adult amphioxus were obviously secretory ones characterized by well-developed peripheral filaments, a prominent Golgi apparatus and abundant apical secretory vesicles. This study also showed that adult amphioxus body surface mucus contained lectin that could agglutinate human red blood cells. The authors propose that the epidermal cells of amphioxus larva and adult may contribute to the immune defense of the amimal by different means. Project 3860811 supported by NSFC and study also supported by the Shandong Natural Science Foundation (Grant No. 92D1144).  相似文献   

12.
A new planktonic dinoflagellate, Prorocentrum donghaiense I_a sp. nov., is described in the present paper. The water sample was collected from the Changjiang Estuary, the East China Sea. The species identification is based on shape, size, surface micro-morphology, ornamentation of thecal plates and the architecture of the pel‘iflagellar area and the intercalary bands as seen by fight and scanning electron microscope. Prorocentrum donghaiense Lu sp. nov. is compared with other prorocentrum species with respect to morphological characteristics and bloom behavior. It is not known whether Prorocentrum donghaiense Lu sp. nov produces phycotoxins like some other Prorocentrum species. Four other red tide species in the family Prorocentraceae (Dinophyceae), namely P. balticum, P. minimum, P.micans, P. triestinum, were examined and identified by light and scanning electron microscope. They have been recorded as bloom-forming species. Some aggregates of Prorocentrum are observed at the end of blooms. An event of strong discoloration caused by P. donghaiense could be detected by satellite sensor in the East China Sea in the late spring, of 1995.  相似文献   

13.
ImODUcrroNTheVertchrateepidennisisinintirnatecontaCtwiththeenvironmentandre~environmentaladaptions.TheepidermisofterreStrialanbolsiskeratinedwhilethatofamPhibiousandaquaticfonnsisrelataltomucus-produCti0n.Theepidennisadsasafi-nalbatherbetweentheorganismanditsenvironmentandoneofitSrnainfunCtionsistoproteCttheorganismagainstextemalpathogens.lnadditiontoIneCanicalproedonofthebody,theepidertnisofamPhibiansandfishescansededinsandotherantibacterialpeptidesthathelpinthebonedefenSeoftheanhal(Su…  相似文献   

14.
The preliminary purification and antimicrobial mechanism of antimicrobial peptide from Antarctic Krill were studied in this paper. The results showed that the molecular weight range of antimicrobial polypeptide (CMCC-1) obtained by cation exchange chromatography was between 245-709D as detected by molecular sieve chromatography, and the minimum inhibition concentration (MIC) of CMCC-1 against Staphylococcus aureus was 5.0 mg mL?1. The antimicrobial mechanism of CMCC-1 was studied with S. aureus as indicator bacterium. Compared with control group, the results of the experimental group in which S. aureus was treated with CMCC-1 were as follows: 1) CMCC-1 could inhibit cell division at logarithmic phase. 2) The protein and reducing sugar content, and the conductivity of culture medium increased, and the activity of alkaline phosphatase and β-galactosidase could be detected in the culture medium. 3) Observation under scanning electron microscope revealed that somatic morphology became irregular, and then somatic surface became coarse. The cell became much smaller, and most somatic cells gathered. The boundary between cells became dim and finally fused as a whole. 4) Observation under transmission electron microscope showed that the surface of S. aureus became rough and the reproducing ability was restrained. The cell wall became thin and the cytoplasm shrunk. Substances inside cell leaked out, which caused cells death. 5) SDS-PAGE analysis showed that some bands disappeared, and the residual bands became vague. 6) The genomic DNA electrophoresis results showed that the genomic DNA bands of S. aureus were not degraded but the brightness significantly reduced. Thus, it is supposed that CMCC-1 could destroy the cell wall and membrane of S. aureu, increase the cell membrane permeability and the leaking-out of intracellular substances, and thus cause the death of S. aureu.  相似文献   

15.
对繁殖季节彩虹鲨卵巢的结构进行显微观察。结果表明,繁殖季节彩虹鲨卵巢,大多处于Ⅳ期和Ⅴ期,少数处于Ⅲ期。在Ⅳ和Ⅴ期卵巢中,Ⅱ~Ⅵ时相的卵母细胞同时存在,说明彩虹鲨为分批产卵类型。Ⅱ时相卵母细胞出现卵黄核,Ⅲ时相卵母细胞出现放射膜和皮质液泡,Ⅳ时相卵母细胞的受精孔和精孔细胞明显。  相似文献   

16.
INTRODUCTIONTheintracellularsurfaceofacellcouldbeobservedbyusingscanningelectronmicroscope(SEM)andthefreezefracturetechnique .Exposingthecellsurfaceisthemostdirectapproach .Inthistechnique,allexposedsurfacescutopenduringsectioningcouldbeviewedbySEM (Russ…  相似文献   

17.
Symbiotic algae from two anemones, Radianthus macrodactylus and Stichodactyla mertensii, found in the South China Sea, were cultivated in ASP-8A medium in this study. Changes of superficial configuration of symbiotic algae during the cultivation were studied by means of a microscope and a scanning electron microscope (SEM). A number of small cavities appeared on the surfaces of symbiotic algae after they were cultivated for 10 h. The cavities enlarged and the cell contents were lost with extended cultivation. Our data suggested that the presence of cavities on symbiotic algae surfaces may be one of the main reasons for failure to culture symbiotic algae in an artificial medium.  相似文献   

18.
按照常规技术进行马氏珠母贝插核育珠,在手术后第1、3、7、15、20、30和60天解剖剪取珍珠囊,利用H E染色等组织化学方法研究马氏珠母贝珍珠囊形成过程中的组织学和组织化学变化。结果表明:珍珠囊表皮细胞来自于移植细胞小片的表皮细胞;在水温27℃条件下,插核后1~3 d来自育珠贝的游走细胞逐渐将细胞小片包围;插核后7~15 d,珠核表面密集来自育珠贝的游走细胞;插核后15~20 d,细胞小片外表皮细胞增殖形成珍珠囊,珍珠囊表皮细胞和细胞核均呈扁平状;插核后20~30 d,扁平状珍珠囊表皮细胞逐渐转变为高柱型,并分泌形成透明的壳皮层物质;在插核后第60天,已形成具有分泌珍珠质功能的扁平状珍珠囊表皮细胞,细胞核呈椭圆形或近圆形。  相似文献   

19.
在透射电子显微镜及环境扫描电子显微镜下观察黄鳍东方鲀精子的超微结构。结果表明:黄鳍东方鲀精子由头部和尾部两部分组成。头部呈长圆柱形,无顶体,核内有小空隙,空隙中有少量电子致密小颗粒存在;核后端正中有凹陷入核内的植入窝,中心粒复合体位于植入窝内,由近端中心粒、中心粒间体和基体组成;袖套位于核的后端,内含线粒体球和含有电子致密物质的小囊泡。尾部细长,自头部后端的正中部向后伸出,近核端部分很短,核心结构是轴丝,鞭毛起始于袖套腔,远核端有侧鳍;轴丝为典型的"9+2"微管对复合体结构。  相似文献   

20.
Lymphocystis nodules occurring in the cultured sting fish Sebastes schlegeli were observed under light and electron microscope. Lymphocystis disease virus (LCDV) in the tissues of diseased fish was detected with indirect immunofluorescence test (IFAT). Results showed that lymphocystis cells had overly irregular nuclei, basophilic intracytoplasmic inclusion bodies with virions budding from the surface, and hyaline capsules outside the cell membrane. Numerous virus particles about 200 nm in diameter scat- tered in the cytoplasm, electron-dense particles 70-80 nm in diameter filled in perinuclear cisterna, and membrane-enveloped parti- cles with electron-dense core of 70-80 nm appeared around cellular nucleus. IFAT using monoclonal antibody against LCDV from Paralichthys olivaceus revealed that specific green fluorescence was present in the cytoplasm of lymphocystis cells, epithelium of stomach, gill lamellae, and muscular fibers under epidermis of S. schlegeli, just as that in the cytoplasm of lymphocystis cells of P. olivaceus, suggesting the presence of LCDV in these tissues.  相似文献   

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