372 resultados para Leymus chinensis


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本文研究了365nm波长紫外线辐射中国对虾精子对其顶体反应和受精能力的影响。结果表明,低剂量紫外线辐射促进精子发生顶体反应,大剂量辐射使精子丧失发生顶体反应的生理机能并死亡。人工诱导雌核发育的过程中,紫外线辐射精液稀释液5-8秒,可获得遗传物质失活的精子(激活源)。经透射电镜观察分析,紫外线对精子遗传物质的损伤是一种使染色质变性的化学作用。

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在过去的几十年间,利用线粒体基因组序列探讨后生动物深层次的系统发育关系已取得初步进展。这主要得益于,线粒体基因组与其它分子标记相比具备诸多优势。迄今为止,超过1,200个后生动物的线粒体基因组已被测定,然而所获得的数据分布极不均衡。 软甲纲历来是甲壳动物分类学和系统发育学研究的重要类群,在形态学特征和分子生物学各方面取得广泛的发展。尽管软甲纲本身作为单系群已得到大多数甲壳动物学家认可,但是软甲纲内部各个类群之间的系统发育关系迄今仍颇有争议。本文报道了凡纳滨对虾Litopenaeus vannamei、中国明对虾Fenneropenaeus chinensis、脊尾白虾Exopalaemon carinicauda、太平洋磷虾Euphausia pacifica和采自南极普里兹湾南极磷虾Euphausia superba的线粒体基因组,其长度分别为15,989 bp、16,004 bp、15,730 bp、16,898 bp和15,498 bp以上(部分非编码区没有测定)。 本研究发现凡纳滨对虾、中国明对虾、脊尾白虾和太平洋磷虾的线粒体基因组包含后生动物线粒体基因组典型的基因组成(13个蛋白质编码基因、22个转运RNA、2个核糖体RNA和一个非编码的AT富含区);然而,南极磷虾与后生动物线粒体基因组典型的基因组成相比,存在1个trnN基因的重复。与泛甲壳动物线粒体基因组的原始排列相比,凡纳滨对虾和中国明对虾线粒体基因组的基因排列完全一致;脊尾白虾的线粒体基因组发生罕见的trnP和trnH易位,从而说明在真虾下目中线粒体基因组的基因排列并不保守;太平洋磷虾线粒体基因组的基因排列出现3个转运RNA的重排 (trnL1、trnL2和trnW);南极磷虾线粒体基因组的基因排列除了出现太平洋磷虾具有的这3个转运RNA重排之外,还有1个trnN的重复和1个trnI基因的重排。另外,在太平洋磷虾线粒体基因组最大的非编码区中存在一个154 bp×4.7的串连重复区域,如此大片段的串联重复区域(>150 bp)在软甲纲动物线粒体基因组中是首次报道。 目前所获得的线粒体基因组数据强有力地支持口足目、对虾科、真虾下目和短尾下目为单系群。通过比较基因排列及蛋白质编码基因核苷酸和氨基酸序列的系统发育分析得知真虾类和龙虾类为腹胚亚目的原始类群,并支持“((Penaeus+Fenneropenaeus)+Litopenaeus)+Marsupenaeus”的系统发育关系。此外,线粒体基因组的数据也强有力地支持磷虾目为单系群。但对于磷虾目在软甲纲中的分类地位及与其它类群的系统发育关系存在一些分歧:基于蛋白质编码基因核苷酸和氨基酸数据的贝叶斯分析强有力地支持磷虾目和十足目近缘,这个结果和传统的分类系统完全一致;然而,基于核苷酸序列的邻接法、氨基酸序列的邻接法和最大似然法均强有力地支持磷虾类和对虾类亲缘关系较近,从而破坏了十足目的单系性,与传统的认识并不一致,但由于自展值的支持率非常高,所以深层次的分析需要进一步加强。 星虫动物属于海洋生物中的一个小门类,自1555年被记载以来,其在后生动物中的分类地位就备受争议。本研究测定了星虫动物门的第一条线粒体基因组:革囊星虫Phascolosoma esculenta的线粒体基因组,全长为15,494 bp,包含13个蛋白质编码基因、22个转运RNA、2个核糖体RNA和1个非编码的AT富含区,所有37个基因在同一条链上编码。与后生动物线粒体基因组的典型组成相比,存在一个trnR基因的缺失和一个trnM基因的重复。比较星虫动物和其它后生动物的线粒体基因组,可以得到以下结论:1)星虫动物和环节动物(包括螠虫动物)的线粒体基因组有相近的基因排列,而且所有基因都在同一链上编码;2)基于蛋白质编码基因的系统发育分析强有力地支持星虫动物和环节动物(包括螠虫动物)组成一个单系群,而将软体动物排除在外。因此,本研究认为以前许多星虫动物和软体动物“共享”的特征,包括发育特征和缺乏分节等,需要重新考虑。

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为更好地管理和开发中国对虾的遗传资源,建立完善的中国对虾优良(抗病)品种的选育计划,该文对中国对虾自然群体和养殖群体进行了遗传多样性评估,并对一个养殖群体进行了抗病性状的遗传育种试验.从CS<,201>筛选个体大、活力强的对虾进行育种试验.CS<,202>和CS<,203>分别为感染WSSV爆发性流行病后存活的第二代和第三代群体.设计口饲毒饵法对CS<,203>进行人工感染,以确定连续选育的中国对虾的抗病能力.利用AFLP(Amplifiedfragmentlengthpolymorphisms)技术分析连续3代群体CS<,201>、CS<,202>、CS<,203>的遗传多样性和遗传标记.RAPD和同工酶的调查结果表明,中国对虾种群的遗传多样性水平低,群体内和群体间的2种分子标记都表现较高的稳定性.群体间比较分析,KP的遗传多样性最高,YB次之,CS<,1>最低.在用同工酶分析的4个群体中,CS<,201>的多态位点比例和杂合度等指标高于其它3个群体.从群体的分化指标来看,中国对虾种群的各群体间有一定的遗传分化.

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三倍体培育是水产动物遗传改良的重要途径之一,它在提高养殖产量、改良品质方面发挥着重要作用。对虾三倍体在性腺发育和性别比率方面与二倍体之间存在明显差异。本论文对三倍体性腺发育的分子机理进行了初步探讨,为阐明甲壳动物的性腺发育和性别控制机理提供重要依据。本论文取得的主要进展如下: 利用联会复合体的分析技术,比较分析了雄性二倍体和三倍体中精母细胞的减数分裂行为。二倍体对虾具有典型的真核生物联会复合体的形态,联会复合体在二价体联会处沿同源染色体长轴分布;未见明显的异型性别染色体;三倍体对虾精母细胞的联会行为复杂,可见二价体、单价体、非同源联会的三价体、同源转换和同源区完全配对的双联会复合体等不同形态;三倍体对虾在晚粗线期普遍表现为三价体同源区完全配对的双联会复合体形态,这种联会行为可能是导致其产生 3n 倍性精子的关键原因。 利用抑制性消减杂交技术,建立了对虾二倍体和三倍体卵巢间的2个消减文库;在正向消减文库(以三倍体卵巢作为实验组,二倍体卵巢作为驱动组)中,鉴定到54个基因;在反向消减文库(以二倍体卵巢为实验组,三倍体卵巢为驱动组)中,鉴定到16个基因;选取11个差异表达的基因,利用半定量RT-PCR的方法对其在二倍体和三倍体卵巢间的表达进行了检测,均能很好地与消减结果相吻合;这些差异基因编码多种功能的蛋白,分析表明染色体的三倍化使三倍体卵巢中的基因调控网络受到了影响;为深入揭示维持卵巢正常发育的关键分子调控事件奠定了基础。 为进一步分析特定基因对对虾性腺发育的调控机制,选取了在对虾三倍体和二倍体卵巢中差异表达显著的 3 个不同基因,PCNA (proliferating cell nuclear antigen)、CAS/CSE1 (cellular apoptosis susceptibility protein/chromosome segregation 1)和 SSRF (spermatogonial stem-cell renewal factor),进行了相关研究分析,为深入探讨特定基因对对虾性腺发育的调控机制以及三倍体中的基因表达调控机制奠定了基础; 中国明对虾PCNA基因在增殖旺盛的性腺组织及造血组织中表达量最高;在二倍体卵巢中的表达水平显著高于三倍体卵巢;在不同病原刺激下的造血组织中的表达模式不同,与对虾对抗不同病原刺激的免疫反应相关;PCNA在序列上的高度保守性,提示了其功能的保守性;利用PCNA基因可以指示细胞的增殖活性的特点,将辅助我们在对虾发育生物学和二倍体、三倍体对虾比较发育生物学的研究; 中国明对虾CAS/CSE1基因在二倍体卵巢中高表达;在卵母细胞中,其mRNA大量分布于细胞质及细胞核周围;是早期胚胎发育的母源性因子;在其氨基酸序列的N端具有importin-β 家族蛋白的保守结构,提示其可能通过参与核质运输在发育过程中发挥重要作用;利用原核表达系统成功地对其进行了体外重组表达,为进一步在蛋白水平上的功能研究提供了条件; 中国明对虾SSRF(暂时命名)基因在三倍体卵巢中高表达;在正常二倍体对虾的神经组织中表达量最高,提示该基因在神经发育中可能发挥重要作用;在氨基酸序列上与胸苷磷酸化酶(TP)具有最高的相似性;利用原核表达系统成功地对其进行了体外重组表达,为进一步在蛋白水平上的功能研究奠定了基础;对对虾SSRF活性蛋白的酶活及功能验证亟待进行。

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对虾病害在世界范围内的广泛传播,给水产养殖和沿海农村经济造成了重大损失。自1993 年对虾白斑病暴发以来,中国明对虾的养殖一直一蹶不振。引起对虾大规模死亡的原因是多方面的,其主要原因是养殖环境恶化、对虾种质退化和抗病力下降。因此,深入开展对虾免疫机制研究,并在此基础上寻找对虾疾病防治的有效方法,改良种质和培育抗病品系,已成为对虾养殖业走可持续发展之路的当务之急。 Toll 样受体(Toll-like receptors, TLRs)家族是进化保守的哺乳动物模式识别蛋白(pattern recognition receptors, PRR),在先天免疫系统中起着非常重要的作用。本研究采用同源克隆和RACE(rapid amplification of cDNA ends)技术从中国明对虾中克隆到Toll 样受体同源基因,并将其命名为FcToll。它全长4115 bp,3’UTR 包含16 个poly A 尾巴,开放阅读框编码931 个氨基酸的多肽。预测的该多肽包含典型的Toll 样受体结构,分为胞外区、跨膜区和胞内区。其中胞外区有信号肽,有16 个富含亮氨酸的重复序列eucine-rich repeats, LRR),并含有2个LRR-C 末端基序和2 个LRR-N 末端基序;跨膜区是23 个氨基酸的一次跨膜结构域;胞内区是含有139 个氨基酸的TIR 结构域(Toll/Interleukin-1R)。克隆 发现FcToll 的基因组结构包含5 个外显子和4 个内含子。系统发生分析揭示FcToll归属于“昆虫型”的无脊椎动物Toll 样受体家族。组织分布研究发现FcToll 在中国明对虾中是组成型表达的,在淋巴器官中表达量较显著。分别利用不同病原体刺激健康的中国明对虾,Real-time PCR 发现该基因在刺激后表达水平呈现不同的表达谱:灭活鳗弧菌(Vibrio anguillarum)注射后5 小时,该基因表达显著 上调;而WSSV(white spot syndrome virus)注射后该基因表达则迅速下调,感染后23 小时内其表达水平均低于对应时间点的对照组。这就表明FcToll 可能参与中国明对虾的先天免疫防御,尤其可能参与入侵弧菌的免疫应答。

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The morphology and infraciliature of two ectoparasitic ciliates, Trichodina caecellae n. sp. and T. ruditapicis Xu, Song & Warren, 2000, parasitising the gills of marine molluscs from the Shandong coast of the Yellow Sea, China, were investigated following wet silver nitrate and protargol impregnation. T. caecellae was found on the small marine sand clam Caecella chinensis Deshayes and is distinguished mainly by the acute triangle-like blade, the very delicate central part and the needle-shaped ray. T. ruditapicis was studied based on four populations from three clams: two populations from Ruditapes philippinarum (Adams) and one each from Saxidomus purpuratus (Sowerby) and Solen grandis Dunker. All four populations fell within the range of morphometry and agreed closely in the overall appearance of the adhesive disc. However, variability was found in the denticle structure, especially in populations from different host clams. Our observations suggest that denticle morphology may be more or less variable between and within populations, and that such minor differences should not be overestimated. It should be emphasised that, except for the denticle morphology, the bright granules or circles in the centre of the adhesive disc represent another important feature facilitating the identification of this trichodinid species.

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A novel manganese superoxide dismutase (MnSOD) was cloned from bay scallop Argopecten irradians by 3' and 5' rapid amplification of cDNA ends (RACE) PCR. The full-length cDNA of MnSOD was of 1207 bp with a 678 bp open reading frame encoding 226 amino acids. The deduced amino acid sequence contained a putative signal peptide of 26 amino acids. Sequence comparison showed that the MnSOD of A. irradians shared high identity with MnSOD in invertebrates and vertebrates, such as MnSOD from abalone Haliotis discus discus (ABG88843) and frog Xenopus laevis (AAQ63483). Furthermore, the 3D structure of bay scallop MnSOD was predicted by SWISS-MODEL Protein Modelling Server and compared with those of other MnSODs. The overall structure of bay scallop MnSOD was similar to those of zebrafish Danio rerio, fruit fly Drosophila melanogaster, Chinese shrimp Fenneropenaeus chinensis, human Homo sapiens, and had the highest similarity to scallop Mizuhopecten yessoensis and abalone H. discus discus. A quantitative real-time PCR (qRT-PCR) assay was developed to detect the mRNA expression of MnSOD in different tissues and the temporal expression in haemocytes following challenge with the bacterium Vibrio anguillarum. A higher-level of mRNA expression of MnSOD was detected in gill and mantle. The expression of MnSOD reached the highest level at 3 h post-injection with V. anguillarum and then slightly recovered from 6 to 48 h. The results indicated that bay scallop MnSOD was a constitutive and inducible protein and thus could play an important role in the immune responses against V anguillarum infection. (c) 2008 Elsevier Ltd. All rights reserved.

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The residues of enrofloxacin and its metabolite in Nile tilapia (Oreochromis niloticus) were studied after oral dose of 50 mg/kg for 7 days. To find the differences between Nile tilapia and Chinese shrimp (Penaeus chinensis), the residues of enrofloxacin in P chinensis were also studied under the same conditions. The results showed that enrofloxacin metabolized into ciprofloxacin in both Nile tilapia and P chinensis, the maximal concentration of enrofloxacin in muscle, liver and plasma of Nile tilapia were 3.61 mu g/g, 5.96 mu g/g, 1.25 mu g/ml respectively, and ciprofloxacin in muscle was 0.22 mu g/g. The maximal concentration of enrofloxacin and ciprofloxacin in P chinensis were 1.68 mu g/g and 0.07 mu g/g respectively. The predicted withdrawal time for Nile tilapia was 22 days, and P. chinensis was 12 days under our experiment conditions. The residues of fitrazolidone [3-(5-nitrofurfurylidenamino)-2-oxazolidinone] and its main metabolite 3-amina-2-oxazolidinone (AOZ) in Nile tilapia were first determined by HPLC/MS. Results showed that after oral dose of 30 mg/kg for 7 days, the maximum concentration of farazolidone in Nile tilapia was 413 mu g/kg after 6 h, whereas AOZ residue reached its maximum (31 mu g/kg) right after stopping treatment. In contrast to the high metabolic rate of furazolidone, AOZ was very difficult to eliminate in vivo, thus the withdrawal time of furazolidone in Nile tilapia was 22 days at least. (c) 2005 Elsevier B.V. All rights reserved.

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Berberine was abstracted from coptis chinensis and its inhibition efficiency on corrosion of mild steel in 1 M H2SO4 was investigated through weight loss experiment, electrochemical techniques and scanning electronic microscope (SEM) with energy disperse spectrometer (EDS). The weight loss results showed that berbefine is an excellent corrosion inhibitor for mild steel immersed in 1M H2SO4. Potentiodynamic curves suggested that berbefine suppressed both cathodic and anodic processes for its concentrations higher than 1.0 x 10(-4) M and mainly cathodic reaction was suppressed for lower concentrations. The Nyquist diagrams of impedance for mild steel in 1 M H2SO4 containing berbefine with different concentrations showed one capacitive loop, and the polarization resistance increased with the inhibitor concentration rising. A good fit to Flory-Huggins isotherm was obtained between surface coverage degree and inhibitor concentration. The surface morphology and EDS analysis for mild steel specimens in sulfuric acid in the absence and presence of the inhibitor also proved the results obtained by the weight loss and electrochemical experiments. The correlation of inhibition effect and molecular structure of berberine was then discussed by quantum chemistry study. (c) 2005 Elsevier B.V. All rights reserved.

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通过标本研究和野外考察,对中国赖草属(Leymus Hochst.)进行了分类修订.结果在中国共确认了3组、33种、7变种赖草属植物,其中多穗组包含4种,少穗组包含24种、7变种,单穗组包含5种,新报道的3个种和新修订的4个类群(即3个新组合和1个新名称)皆隶于少穗组.同时对赖草属的研究简史、属的形态特征和一些类群的地理分布也分别作了简要介绍.

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根据标本研究、野外考察和实验观察,对国产赖草属Leymus两个类群进行了分类修订,将阿尔金山赖草Leymus arjinshanicus D.F.Cui和L.aerginshanicus D.F.Cui ssp.ruoqiangensis(S.L.Lu&Y.H.Wu)D.F.Cui处理为若羌赖草L.ruoqiangensis S.L.Lu&YH.Wu的新异名,将纤细赖草L.secalinus(Georgi)Tzvel.var.tenuis L.B.Cai提升为一个独立的种L.tenuis(L.B.Cai)L.B.Cai.

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报道了新疆赖草属2个新变种,即北疆赖草(Leymus tianschanicus(Drob.)Tzvel.var.borealus L.B.Cai)和短穗赖草(Leymus angustus(Trin.)Pilger vat.brevistachyus L.B.Cai)。

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报道了青海赖草属植物一新种:圆稃赖草(Leymus oblongolenmatus L.Zhi et L.B.Cai)。该种的主要特征如下:多年生草本,杆直立、光滑、疏丛,高60~90cm。叶鞘粗糙,边缘膜质,长于或短于节间,叶舌膜质;叶片边缘内卷。穗状花序直立、密集、黄绿色,长10~15cm,宽5~15mm,穗轴粗糙,小穗常3~4枚生于每节,含3~6小花;颖披针形,长4~7mm,具3~5脉,边缘膜质;外稃长圆状披针形,不明显3脉,背部疏生短柔毛;花药黄色,长4~5mm。该种与L.paboahus相似。

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对国产赖草属15个种的叶片表皮进行了光镜观察,发现下表皮呈现的微形态差异可以把国产类群划分为3个群体,并参照各群体所具的外部形态特征,3个群体应分别属于前人组群划分中的3个组,即多穗组(sect.Leymus)、少穗组(sect.Aphanoneuron(Nevski)Tzvelev)和单穗组(sect.Anisopyrum(Griseb.)Tzvelev).同时,根据叶表皮性状的递变趋势,分析了3个国产组的亲缘关系.结果表明:多穗组最原始,单穗组最高级,少穗组演化居中;单穗组与少穗组亲缘关系直接,与多穗组关系间接.

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根据样方调查资料,采用聚类分析法,研究了青海湖区针茅草原围栏封育后植物群落特征及群落多样性变化。结果表明,草原经过长期围栏后,群落内优势种发生了不同程度的分异,由围栏外的紫花针茅(Stipa purpurea)+青海苔草(Carex ivanovae)草原演变成围栏内的冷地早熟禾(Poa crymophila)+猪毛蒿(Artemisia scoparia)草原群落,导致了群落结构特征的变化;长期的围栏活动对提高草原群落的盖度和生产能力是有益的,但却降低了群落的物种丰富度和多样性;草原开垦后,对周围草原有明显的影响,所形成土垄的群落特征和多样性变化都发生了极大的差异,成为赖草(Leymus secalinus)+大籽蒿(Atremisia sieversiana)群落类型,群落的物种丰富度和多样性均降低。