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61.
通过对不同水温(17、21、25、29、33和37℃)下,龙虎斑幼鱼的摄食生长、血清抗氧化酶(SOD、CAT)活力、消化酶活力及鱼体体成分含量变化等的分析,探讨龙虎斑(Epinephelus lanceolatus♂×Epinephelus fuscoguttatus♀)幼鱼的最适生长温度范围。结果表明:(a)在养殖水温17~33℃范围内,龙虎斑幼鱼最佳摄食生长水温范围为30.20~31.29℃。(b)养殖水温对幼鱼SOD、CAT酶活性影响显著(P<0.05)。(c)养殖水温对龙虎斑幼鱼的蛋白酶活性有显著影响,肠脂肪酶在21℃显著高于其他温度组(P<0.05);肠淀粉酶在25℃时显著高于其他组(P<0.05);蛋白酶活性最适水温为27.82~31.44℃。血清磷酸酶ACP和AKP活性在低温17℃时活性显著高于其他组(P<0.05),肝胰脏中磷酸酶ACP和AKP活性在低温33℃时活性低于其他组。(d)养殖水温对幼鱼体成分含量有显著影响(P<0.05),且随养殖水温的升高幼鱼水分含量、粗蛋白含量和灰分含量呈先降后升的变化趋势;脂肪含量则相反。  相似文献   
62.
A new cell line,CSEC,has been successfully established from embryos at gastrula stage of a cultured marine fish,half smooth tongue sole(Cynoglossus semilaevis).CSEC cells grow actively and stably more than 50 passages for over 200 d in DMEM medium supplemented with 15% FBS(fetal bovine serum),2.5 ng/cm 3 bFGF(basic fibroblast growth factor),1 ng/cm 3 LIF(leukemia inhibitory factor) and 50 mmol/dm 3 2-ME(2-mecaptoethanol).The cells grew well in the temperature range of 24-30 ℃ and the optimal growth temperature was 24℃.FBS and bFGF concentrations are the two key components for CSEC cells proliferation.Chromosome analysis reveals that CSEC cells have a normal diploid karyotype with 2n=42t.The significant fluorescent signals were observed in CSEC after transfection with the GFP reporter gene,suggesting that the CSEC cell line can be used as a useful tool for transgenic and genetic manipulation studies.CSEC cells showed the cytopathic effect(CPE) after infection with lymphosystis disease virus(LCDV) in 2 d.Moreover,the LCDV particles can be observed in the cytoplasm of virus-infected cells by electron microscopy.It suggests that CSEC could be potentially used for the study of aquatic virus.  相似文献   
63.
通过控制暂养水体盐度,用盐度突变与盐度渐变2种方法测定长蛸的盐度耐受性.测定了长蛸血细胞密度、各类血细胞数量比例以及各种酶的活力几组数据,并分析其血细胞与体内酶活力的变化.结果表明:长蛸的生存盐度范围为7.0~30.3,适宜盐度范围为16.3~27.3,最适盐度范围为18.3~24.3,对盐度的适应范围较广,有利于长蛸大规模养殖的开展.在盐度胁迫下,长蛸血细胞密度,各种血细胞数量比例均发生显著改变,长蛸个体也随着胁迫加大变得越来越不适应,出现喷墨、休克、甚至死亡,这表明长蛸的免疫机能降低.无论在低盐度还是高盐度胁迫情况下,受渗透压的影响,长蛸肌体大量吸水和失水,呼吸作用减弱,体内供氧降低,导致长蛸体内有氧呼吸降低和无氧呼吸提高,于是催化有氧呼吸的LDH酶活力降低.同时,细胞内与免疫和消化相关的细胞器由于细胞吸水或失水作用功能受到影响,保护酶(SOD、POD、CAT)、磷酸酶(ACP、AKP)和消化酶(蛋白酶和脂肪酶)的活力均呈下降趋势.由此可见,盐度胁迫对长蛸的影响是显著的.  相似文献   
64.
大黄鱼肌肉组织cDNA全长文库的构建及EST分析   总被引:1,自引:0,他引:1  
黄伟  薛良义  李婷  杨斌 《台湾海峡》2010,29(2):189-195
以大黄鱼肌肉组织为材料,利用Creator Smart cDNA Library Construction Kit构建了大黄鱼肌肉组织的全长cDNA文库.文库质量分析表明:cDNA文库容量不低于1.68×106cfu/mm3,重组率达96%,插入片断的平均长度大于1 000bp.随机挑取512个cDNA克隆进行5’端测序,其中430条ESTs的长度大于100bp;并初步拼接得到了230个单基因簇(unigene),其中包括58个重叠群(contigs),172个单拷贝ESTs(singletons),冗余度为46.51%.经检索,35个ESTs在BLASTx上无明显的同源性(E值≤1.00×10-10),为新基因.195个ESTs与已报道的基因有较高的同源性;其中与能量相关基因的ESTs丰度最高,占总数的20.00%.蛋白质合成、细胞骨架和信号传导次之,比例分别为13.48%、12.17%、10.00%,其中包括高迁移率族蛋白B1、瘦素受体、β1-热激蛋白等.这些EST数据为进一步筛选和克隆大黄鱼肌肉特异性表达基因提供了平台.  相似文献   
65.
黑鱾血液的生理生化指标研究   总被引:2,自引:0,他引:2  
孙敏  徐善良  唐道军 《台湾海峡》2009,28(4):482-487
本文采用F-820半自动血细胞分析仪和全自动生化分析仪,对黑纪的血液常规指标及血清中的17项生化指标进行了分析测定,并用Wright’s染色法制作血涂片对白细胞进行分类计数.结果表明:(1)黑纪的血红细胞数量为(2.49±0.47)×10^12个/dm^3;白细胞数量为(1.08±0.21)×10^11个/dm^3;在白细胞中以嗜中性粒细胞数量最多,占52.42%±4.67%,其次为淋巴细胞,占25.72%±2.88%;单核细胞体积最大,占总数的3.27%±0.62%.(2)黑纪红细胞脆性大,抗性差,在0.65%~0.70%的NaCl溶液中开始溶血,在0.50%~0.55%的NaCl溶液中完全溶血.(3)黑纪的血红蛋白(HGB)为109.11±15.72g/dm^3,高于一般鱼类,与其较强的耐低氧生理能力相适应.(4)血清中血糖浓度为4.72±1.35mmol/dm^3,明显低于凶猛肉食性鱼类,与其岛礁性生态习性和杂食性相吻合.(5)雌雄鱼的乳酸脱氢酶分别为332.67±188.48U/dm^3和905.66±257.85U/dm^3,雌鱼显著高于雄鱼,可能与繁殖活动相关.  相似文献   
66.
采用饲养对比试验方法,研究了谷氨酰胺二肽(Gin二肽)对日本对虾血清生化指标、肝胰腺细胞凋亡和肠绒毛的影响及对虾体健康的作用。结果表明,饲喂Gin二肽各组的PO、LSZ、ACP含量均显著(P〈0.05)高于对照组,添加0.5%和1.0%Gin二肽组的SOD和ALP含量也显著(P〈0.05)高于对照组:添加1.0%Gin二肽的TP含量显著(P〈0.05)高于其它各组。血清TP、PA、UN、CHO、PO、LSZ、SOD、ALP、ACP和LDH等各项指标均随Gin二肽添加量的提高而呈现增加趋势。试验建立了流式细胞术检测对虾肝胰腺细胞凋亡率的方法;肝胰腺细胞凋亡率随着日粮Gin二肽添加量的增加而显著降低(P〈0.05)。肠道切片显微观测结果表明,添加1.0%的Gin二肽能显著增加日本对虾肠绒毛高度(P〈0.05)。饲料中添加Gin二肽可显著提高日本对虾血清中的溶菌酶、抗氧化酶及磷酸酶活性,降低肝胰腺细胞凋亡率,增加肠绒毛高度,改善虾体健康状况。  相似文献   
67.
We extracted marine low-temperature lysozyme (MLTL), a novel lysozyme, from a marine microorganism through fermentation. Our previous study suggested that a low molecular weight (16 kDa) may exert anti-tumor activity through antiangiogenesis. In this study, we extracted a high weight (39 kDa) and investigated its antiangiogenic activity in vivo and in vitro. Using zebrafish embryos as an in vivo study model, we found that treatment with MLTL significantly inhibited the growth of subintestinal vessels (SIVs) in a dose-dependent manner and that 400 μg/ml MLTL was sufficient to block the growth of SIVs. An in vitro study conducted using human umbilical vein endothelial cells (HUVECs) revealed that MLTL suppressed the proliferation, migration and tube formation of HUVECs in a dose-dependent manner. Interestingly, assays by flow cytometry and DNA electrophoresis indicated that MLTL was able to induce apoptosis of HUVECs. Moreover, further study demonstrated that the disruption of intracellular Ca2+ homeostasis may play an important role in MLTL induced apoptosis of HUVECs. Taken together, the results of this study demonstrate for the first time that MLTL inhibits angiogenesis through its pleiotropic effects on vascular endothelial cells and induces apoptosis through regulation of cellular Ca2+ levels. The results of this study also revealed a possible mechanism underlying the antiangiogenic effect of MLTL and suggested that MLTL may be a promising new antiangiogenic agent for use in cancer therapy.  相似文献   
68.
为了探明姬松茸提取物的体外抗病毒感染活性及其作用方式,进而为水产养殖鱼类高效抗淋巴囊肿病毒(lymphocystis disease virus,LCDV)感染活性物质的开发和鲆蝶类淋巴囊肿病的防治奠定基础,利用热水浸提和酒精沉淀法得到了5种姬松茸提取物组分(E1~5),并利用MTT、细胞病变程度观察等方法研究了5种组分对LCDV感染体外培养大菱鲆鳍细胞(turbot fin cells,TF细胞)的影响作用.细胞毒性实验结果显示,5种组分对体外培养TF细胞均无毒性.细胞病变程度结果表明,本文所得5种姬松茸提取物组分尤其是E5组分具有显著的抗LCDV感染TF细胞的活性.不同方式感染的实验结果进一步显示,5种姬松茸提取物组分抗LCDV感染TF细胞的作用可能主要是通过直接灭活病毒和/或阻断病毒吸附细胞来实现的.  相似文献   
69.
Timing of vegetal-endodermal cell determination in amphioxus embryos remains uncertain. We tentatively tested effects of A23187, the calcium ionophore, on the development of vegetal blastomeres isolated at the 16-cell stage. It was found that when vegetal blastomeres committed to endoderm were treated with A23187 prior to gastrulation, they were transformed into ectodermal cells as evidenced by the cell morphology and function characteristic of epidermis. However, the developmental fate of the same blastomeres untreated or treated with DMSO at the same stage or of those treated with A23187 after gastrulation remained unchanged. Thus, vegetal-endodermal cells in amphioxus embryos are not irreversibly determined before the gastrula stage, and artificial increase in intracelluar Ca2+ concentration can induce transdetermination of the predetermined endodermal cells into ectodermal cells. Project 39470091 supported by NSFC and partly supported by Shandong Natural Science Foundation, Grant No.93D0140.  相似文献   
70.
Sun  Xiujun  Liu  Zhihong  Zhou  Liqing  Wu  Biao  Yang  Aiguo  Tian  Jiteng 《中国海洋大学学报(英文版)》2020,19(2):386-392
Though the larval development of bivalves has been extensively studied for commercial purposes,the dynamic development of larval muscle system remains largely unknown.In this study,we characterized the larval muscle system at different developmental stages(D-shaped veligers,umbo veligers and spats)in the bay scallop(Argopecten irradians)by phalloidin staining and under a confocal microscopy.The functional muscles are initially established at the early stage of veligers,which have four pairs of velar retractors and one anterior adductor.At the veliger stage,the velum and posterior retractor muscles are functionally important for velar contractility but undergo an irreversible shrink until they disappear at the end of the larval stage.During metamorphosis,three crucial modifications take place in the larval muscle system.The metamorphosis process involves the gradual degeneration of velum retractors,mantle margin development from an unfolded to a three-fold state,and remodeling of the adductor muscle system from dimyarian(two adductors)to monomyarian condition(one adductor)as in juveniles/adults.All retractor muscles are composed of striated muscle,but both anterior and posterior adductors have smooth and striated components.These findings highlight that the morphological changes at different stages are typical features of myogenesis in scallops.The present knowledge on the developmental dynamics of myogenesis in the bay scallop will not only improve our understanding of phenotypic diversity of larval myoanatomy in bivalves,but also provide useful information on the larval culture in hatcheries.  相似文献   
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