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1.
采用RNAi技术研究了栉孔扇贝(Chlamysfarreri)foxl2基因在卵子发生和卵巢功能维持中的作用。使用体外合成的栉孔扇贝foxl2双链RNA(dsRNA),以每只50μg/次的剂量注射进闭壳肌中,连续注射2次(第一次注射后7天,再进行第二次注射);以注射相同体积PBS(相同注射方法)的扇贝作为阴性对照组,以不注射扇贝作为空白对照组。qRT-PCR检测干扰组扇贝卵巢中的foxl2 mRNA表达量较空白对照组下降了62%, Western blotting检测该蛋白在卵巢中的含量也明显下降,显示靶基因的表达水平被有效地敲降。组织学观察发现,栉孔扇贝foxl2干扰后的卵巢中卵母细胞形态异常、细胞核固缩,卵子发生明显受阻。表明该基因在栉孔扇贝卵子发生中起重要作用。  相似文献   
2.
卵形鲳鲹早期卵子发生显微及超微结构的研究   总被引:4,自引:1,他引:4  
本文研究了卵形鲳鲹早期卵子发生的显微与超微结构特点。研究结果表明在1~2龄鱼卵巢中卵原细胞进入首次成熟分裂前期的结构特点,3~4龄鱼才开始进入小生长期,文中讨论了此鱼性腺成熟的年龄以及如何加速性腺发育,为人工繁殖提供科学依据。  相似文献   
3.
The sea pen Funiculina quadrangularis (Pallas, 1766) is a species of conservation concern in Scottish coastal waters, due to its restricted geographical distribution and high sensitivity to demersal fishing activities. Reproduction in F. quadrangularis was investigated in a population located in southern Loch Linnhe, west Scotland. This was accomplished through the analysis of trends in oocyte size-frequency distribution and relative fecundity over a 12-month period. Funiculina quadrangularis is dioecious and the study population exhibited a sex ratio of 1:1. Oogenesis in female F. quadrangularis is characterised by the maintenance of a large pool of asynchronously developing oocytes throughout the year, of which a small proportion (<10%) mature with increasing sychronicity and are spawned in midwinter. The reasons for this distinct pattern of oogenesis and winter spawning remain unclear, although the potential influence of environmental cues and the role of endogenous factors in relation to this sea pen's deep-sea habit are discussed. Whilst the duration of oogenesis is prolonged (>12 months), it is proposed that spawning is a brief and synchronous annual event. Relative fecundity is high and is independent of colony size, varying between approximately 500–2000 oocytes per 1 cm rachial midsection. This measure of fecundity exhibited pronounced seasonality and was significantly lower during the post-spawning winter months. Total fecundity in F. quadrangularis is considered to be high; although a small proportion of the total number of oocytes is spawned annually, this is compensated for by large colony size. Funiculina quadrangularis produces large oocytes (>800 μm), indicative of the production of lecithotrophic larvae.  相似文献   
4.
Despite the wide distribution of zoanthids, little is known about their pattern of reproduction. Here we investigate the reproductive biology of two Mediterranean species, the common Parazoanthus axinellae (Schmidt) and the rare Savalia savaglia (Bertoloni). For both species, samples were collected during an annual cycle, from January to December 2005, in the Western Mediterranean (Ligurian Sea, Italy). Both species are gonochoric. In P. axinellae the sex‐ratio (n colonies = 30) showed a slight predominance of male colonies (M/F = 1.35), whereas in the population of S. savaglia (n colonies = 15) a predominance of females was found (M/F = 0.3). In P. axinellae the first gametocytes were visible in March, whereas in S. savaglia they became visible in May. Both species reproduce at the end of autumn when seawater temperature begins to decrease. Parazoanthus axinellae (10 m depth) spawns eggs and sperms in November, whereas S. savaglia (67 m depth) spawns in December. In P. axinellae sexes were segregated on a rocky wall, with males occurring deeper, whereas male and female colonies of S. savaglia were irregularly dispersed in the population. The maximum number of oocytes differed between the species, being higher in P. axinellae than in S. savaglia.  相似文献   
5.
澳洲管体星虫(Siphonosoma australe)是海南当地极具特色的星虫资源, 经济价值高。近年来该资源急剧衰竭, 开展星虫资源恢复与保护十分重要。文章对海南澳洲管体星虫卵细胞的显微与超微结构进行研究。结果显示: 1) 卵细胞发育经历4个阶段: 生长前期, 体腔液中大量光滑的凹饼状红细胞出现表面凹凸不平的褶皱(直径小于30μm), 暗示这些红细胞是卵原细胞; 生长后期, 30~40μm的卵细胞表面褶皱消失, 变成光滑的圆厚饼状, 并出现厚度1μm的卵黄膜, 卵黄颗粒开始积累; 成熟前期, 卵细胞球状, 直径60~120μm, 卵黄膜增厚至5~11μm, 卵黄颗粒增多, 细胞核增大, 部分染色质形成高电子密度的团块散布于核内; 成熟后期, 直径120μm, 卵黄膜厚11~12μm, 卵黄颗粒充满整个卵细胞, 膜孔外露于膜表层。2) 成熟期澳洲管体星虫卵黄膜仅分为两层: 有一定厚度的均质内层和多层重叠膜结构组成的外层, 同时外层上覆盖有粒状突。膜孔结构简单, 主要是膜凹陷折叠形成。3) 卵黄颗粒分为Ⅰ型和Ⅱ型, 其发生途径主要由线粒体、内质网、高尔基体和溶酶体等细胞器演变而成, 亦可由卵母细胞吞饮而成。最为常见的是高尔基体包裹形成的Ⅱ型卵黄颗粒。4) 海南文昌海域澳洲管体星虫的繁殖季节为4—8月, 其中5—7月是繁殖高峰期。3月初卵母细胞开始出现, 4—8月成熟卵细胞在体腔中保持一定密度, 9月份卵细胞密度降至极低, 10月份后消失。澳洲管体星虫作为一种新的具有热带特色的水产种质资源, 其卵细胞发育及生殖周期研究将极大推动其繁育及保护的相关技术探索。  相似文献   
6.
光裸星虫体腔液中卵子发生的超微结构   总被引:3,自引:0,他引:3  
为探究光裸星虫卵子发生的细胞学特点,利用电镜技术观察了光裸星虫体腔液中卵子发生过程的超微结构变化。结果表明:(1)光裸星虫体腔液中存在游离的卵原细胞和卵母细胞,卵母细胞的发育分为卵黄形成前期、卵黄形成初期、卵黄旺盛合成期和成熟期4个阶段。(2)卵原细胞的细胞器少,核质比大。卵黄形成前期,卵母细胞的细胞器有所增加,大量核仁外排物进入胞质中;出现卵黄膜和胶质膜,卵黄膜遍布微孔。卵黄形成初期卵母细胞核有较多突起,细胞器大量增加,出现分散分布的卵黄粒。卵黄旺盛合成期卵母细胞迅速增大,卵黄大量积累。成熟期卵母细胞核膜突起回缩,胶质膜易于脱落。(3)卵黄分为2种。Ⅰ型卵黄电子密度高,不发生融合,为内源性卵黄;II型卵黄中等电子密度,可融合为无定形卵黄块,为外源性卵黄。(4)成熟卵母细胞卵黄膜为三层,外层为颗粒层,表面具有粒状突;中层初始为均质结构,不断增厚并纤维化;内层致密,厚度不均。胶质膜电子密度极低。(5)卵子外有滤泡细胞,其核质比很大,细胞器少,在卵母细胞成熟期发生凋亡。文章还探讨了胶质膜、卵黄膜、滤泡细胞的功能,以及细胞器在卵黄形成中的作用。研究结果积累了光裸星虫卵子发生细胞学资料,为光裸星虫生殖调控与人工繁育研究提供理论参考。  相似文献   
7.
对不同发育阶段的企鹅珍珠贝[Ptedapenguin(Rding)]的性腺结构、生殖细胞结构与分布进行组织学观察,描述精/卵子发生过程中各级精/卵细胞的特征。结果表明:根据雌性生殖细胞形态和卵黄的变化特点,卵子发生经历卵原细胞、无卵黄初级卵母细胞、卵黄形成期卵母细胞及成熟卵子阶段;依据雄性生殖细胞大小和细胞核形态变化,精子发生经历精原细胞、初级精母细胞、次级精母细胞、精子细胞和精子阶段,其中精原细胞存在形态上有差异的A型和B型两种类型。此外还观察到企鹅珍珠贝的性别转化现象。  相似文献   
8.
Information on the reproductive development of species of box jellyfish (class Cubozoa) is poor globally, despite their significance as potent stingers and worrying projections about range expansions. While most species are confined to tropical and subtropical waters, the South African box jellyfish Carybdea branchi is commonly found in the cold-water (especially southern) Benguela ecosystem. Its biology is unknown. Here, we examine reproductive development and describe gametogenesis in this dioecious species. Four and five maturity classes were determined for males and females, respectively, as well as five oocyte developmental stages. Oocyte sizes differed significantly between developmental stages. Mature and immature medusae differed significantly in size, but males and females did not. Individuals matured at approximately 30 mm average bell dimensions. Carybdea branchi displayed gonadal development characteristic of a semelparous organism.  相似文献   
9.
Pasiphaea multidentata is a deep‐water caridean shrimp fished in the Mediterranean in association with the commercially exploited red‐shrimp Aristeus antennatus. A previous study describes seasonality in the reproductive pattern of P. multidentata using external morphological parametres. This study assesses the spatio‐temporal variations in the population structure, sex ratio, ovary cycle and gametogenesis of P. multidentata from three different fishing grounds in the Blanes canyon and adjacent margin (North‐western Mediterranean) over an annual cycle. The oogenetic pattern of this species is typical of a caridean shrimp. There is a pool of previtellogenic oocytes at all times that develop from the periphery of the gonad towards the centre during maturation. Previtellogenic oocytes grow to approximately 200 μm before undergoing vitellogenesis. The vitellogenic oocytes are surrounded by a monolayer of accessory cells. The maximum size observed for a mature oocyte was 1420 μm. The oocyte‐size distribution confirmed the seasonal reproductive pattern of this species; in winter, the ovaries contained mainly previtellogenic oocytes, some of which start maturing in spring, resulting in a slightly bimodal distribution. In summer, the vitellogenic oocytes reach approximately 1000 μm and in late autumn the ovaries are fully mature and ready to spawn. There were no significant differences in the reproductive and population structure patterns of P. multidentata among the three sites, suggesting that the population’s distribution is not affected by the geomorphology of the area, in particular the presence of the canyon. The populations are dominated by females at all sites and all seasons, with the arrival of juveniles in spring. The seasonal variations in the reproduction and recruitment of P. multidentata and the lack of spatial segregation within the population are discussed in terms of the species’ known biology, the effects of canyons in energy supply to the deep‐sea floor and the relationships of this species with the red‐shrimp A. antennatus.  相似文献   
10.
UltrastructuralstudyofoogenesisinXiamenamphioxus¥FangYongqiangandQiXiang(ReceivedApril10,1993;acceptedJuly9,1993)Abstract:─—U...  相似文献   
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