养殖鲥鱼性腺发育的研究

经激素处理和生态调控的养殖鲥鱼,能完成性腺发育的全过程,其可分为６个时期,卵细胞发育可相应分为６个时相。与其它鱼类不同,细胞中液泡最早出现在胞质的内缘而不是外缘。大、小核仁数随卵母细胞的发育而变化。成熟卵巢成熟系数为８５４％～１２６４％。成熟期卵径为６２８５～８３５３μｍ、精子头径为０７４～１５５μｍ。达性成熟的鲥鱼,冬季卵巢为Ⅱ期、精巢为Ⅱ～Ⅲ期。精、卵巢发育呈现出明显的不同步现象。前者５月底开始进入成熟期,后者７月初进入成熟期。初级卵母细胞由Ⅱ时相发育到Ⅳ时相基本上是同步的。第Ⅳ期卵巢卵径的频率仅出现１个高峰。养殖鲥鱼属１年１次产卵类型。     

瓣结鱼[Tor brevifilis（Peters）]的性腺发育及周年变化

首次描述了瓣结鱼精巢和卵巢的外部形态和组织学结构,记述了精子和卵子的形成过程,参照鲢,鳙鱼的性腺发育的划分标准,依形态学特征将其性腺的发育分为６个时期据组织学特点将雌雄性细胞的变化各分为６个时相。     

养殖Shi鱼性腺发育的研究

经激素处理和生态调控的养殖Ｓｈｉ鱼,能完成性腺发育的全过程,其可分为６个时期,卵细胞发育可相应分为６个时相。与其它鱼类不同,细胞中液泡最早出现在胞质的内缘而不是外缘。大、小核仁数随卵母细胞的发育而变化。成熟卵巢成熟系数为８．５４％￣１２．６４％。成熟期卵径为６２８．５￣８３５．３μｍ、精子头径为０．７４￣１．５５μｍ。达性成熟的Ｓｈｉ鱼,冬季卵巢为Ⅱ期、精巢为Ⅱ￣Ⅲ期。精、卵巢发育呈现出明显的不同     

家蝇的卵子发生的研究——Ⅰ.家蝇卵子发生过程

叙述了家蝇的卵子发生过程:根据卵室的形状与大小,卵室内卵母细胞的体积与营养细胞的比例,营养细胞核的变化,滤泡细胞的分化,边缘细胞的形成及卵壳形成等标准,将卵子发生分为了十一阶段,第一阶段在卵原区内,称为卵原囊,第二阶段为卵室形成,第三至第五阶段,卵室圆形,主要根据营养细胞核内染色体的形状划分,第六阶段卵室成椭圆形,并开始迅速生长;第七阶段卵母细胞占卵室四分之一,边缘细胞于此时发生。第八阶段卵母细胞占卵室三分之一,在营养细胞上的滤泡细胞开始退化至消失,营养细胞核出现灯刷染色体,第九阶段卵母细胞占卵室二分之一:第十阶段占四分之三,卵壳分泌形成,营养细胞开始退化。第十一阶段,营养细胞及滤泡细胞全部退化消失,形成卵。 描述了卵母细胞、营养细胞与核,滤泡细胞在发育各阶段中的变化,并讨论了其意义。     

影响猪体细胞核移植重构胚体外发育的若干因素

以卵丘细胞为核供体细胞组成重构胚,卵裂率达到56.7%,发育至桑椹胚达11.7%、孵化囊胚率为6.7%,显著高于成纤维细胞组成的重构胚(p<0.05)。我们研究了卵母细胞的采集方法,激活方法和卵龄对卵丘细胞核移植重构胚体外发育的影响。以血清饥饿法将卵丘细胞诱导至GO或G1期,抽吸法/解剖法采集卵母细胞,体外培养33或44 h,将卵丘细胞置于去核卵母细胞的卵周隙中,重构胚以钙离子载体A23817或电脉冲结合6-DMAP激活处理,体外培养6天,结果表明,卵母细胞采集方法、激活液中细胞松弛素(CB)并不影响重构胚的发育(以卵龄44h的卵母细胞为受体);而以电脉冲结合6-DMAP激活处理能提高重构胚发育能力(以卵龄33 h的卵母细胞为受体)(p<0.05)。本研究显示,以电脉冲结合6-DMAP激活卵丘细胞重构胚,能在体外发育至囊胚     

猪体细胞核移植重构胚的体外发育

以卵丘细胞为核供体细胞组成重构胚,卵裂率达到56．7％,发育至桑椹胚率达到11．7％,囊胚率为6．7％,显著高于成纤维细胞重构胚（P＜0．05）。本文还研究了卵母细胞的采集方法、激活程序和卵龄对卵丘细胞核移植重构胚体外发育的影响。以血清饥饿法将卵丘细胞诱导G0/G1期,抽吸法／解剖法采集卵母细胞,体外培养33－44h,将卵丘细胞放至去核卵母细胞的卵周隙中,重构胚以钙离子载体A23817或电脉冲结合6－DMAP激活处理,体外培养6d。研究表明,卵母细胞采集方法、激活液中细胞松驰素（CB）、激活程度并不影响重构胚的发育（以卵龄44h的卵母细胞为受体）;而以电脉冲结合6－DMAP激活处理能提高重构胚发育能力（以卵龄33h的卵母细胞为受体）（P＜0．05）。本研究显示,以电脉冲结合6－DMAP激活卵丘细胞重构胚,体外能发育至囊胚。     

影响猪体细胞核移植重构胚体外发育的若干因素

以卵丘细胞为核供体细胞组成重构胚,卵裂率达到56．7％,发育至桑椹胚达11．7％、孵化囊胚率为6．7％,显著高于成纤维细胞组成的重构胚（P＜0．05）。我们研究了卵母细胞的采集方法,激活方法和卵龄对卵丘细胞核移植重构胚体外发育的影响。以血清饥饿法将卵丘细胞诱导至G0或G1期,抽吸法／解剖法采集卵母细胞,体外培养33或44h,将卵丘细胞置于去核卵母细胞的卵周隙中,重构胚以钙离子载体A23817或电泳冲结合6－DMAP激活处理,体外培养6天,结果表明,卵 母细胞采集方法、激活液中细胞松弛素（CB）并不影响重构胚的发育（以卵龄44h的卵母细胞为受体）;而以电脉冲结合6－DMAP激活处理能提高重构胚发育能力（以卵龄33h的卵母细胞为受体）（P＜0．05）。本研究显示,以电脉冲结合6－DMAP激活卵丘细胞重构胚,能在体外发育至囊胚。     

黄胫小车蝗卵子发生及卵母细胞凋亡的显微观察

对黄胫小车蝗(Oedaleus infernalis)卵子发生过程和卵母细胞凋亡进行显微观察。结果表明,黄胫小车蝗卵子发生可明显分为3个时期10个阶段,即卵黄发生前期、卵黄发生期和卵壳形成期。第1阶段,卵母细胞位于卵原区,经历减数第一次分裂;第2阶段,卵母细胞核内染色体解体成网状,滤泡细胞稀疏地排列在卵母细胞周围;第3阶段,滤泡细胞扁平状,在卵母细胞周围排成一层;第4阶段,滤泡细胞呈立方形排在卵母细胞周围;第5阶段,滤泡细胞呈长柱形排在卵母细胞周围,滤泡细胞之间、滤泡细胞与卵母细胞之间出现空隙;第6阶段,卵母细胞边缘开始出现卵黄颗粒;第7阶段,卵母细胞中沉积大量卵黄,胚泡破裂;第8阶段,滤泡细胞分泌卵黄膜包围卵黄物质;第9阶段,滤泡细胞分泌卵壳;第10阶段,卵壳分泌结束,卵子发育成熟。卵母细胞发育过程中的凋亡发生在卵黄发生前期,主要表现为滤泡细胞向卵母细胞内折叠,胞质呈团块状等特征。     

猪体细胞核移植重构胚的体外发育(英文)

以卵丘细胞为核供体细胞组成重构胚 ,卵裂率达到 5 6.7% ,发育至桑椹胚率达到1 1 .7% ,囊胚率为 6.7% ,显著高于成纤维细胞重构胚 (P <0 .0 5 )。本文还研究了卵母细胞的采集方法、激活程序和卵龄对卵丘细胞核移植重构胚体外发育的影响。以血清饥饿法将卵丘细胞诱导至G0 G1 期 ,抽吸法 解剖法采集卵母细胞 ,体外培养 3 3～ 44h ,将卵丘细胞放至去核卵母细胞的卵周隙中 ,重构胚以钙离子载体A2 3 81 7或电脉冲结合 6 DMAP激活处理 ,体外培养 6d。研究表明 ,卵母细胞采集方法、激活液中细胞松弛素 (CB)、激活程序并不影响重构胚的发育 (以卵龄 44h的卵母细胞为受体 ) ;而以电脉冲结合 6 DMAP激活处理能提高重构胚发育能力 (以卵龄 3 3h的卵母细胞为受体 ) (P <0 .0 5 )。本研究显示 ,以电脉冲结合 6 DMAP激活卵丘细胞重构胚 ,体外能发育至囊胚     

不同卵龄小鼠卵母细胞激活和受精的比较研究(英文)

本实验比较了不同卵龄的小鼠卵母细胞受酒精人工刺激后的激活率和体外受精率,以探讨卵母细胞激活和受精的机制。向ＮＩＨ雌鼠腹腔注射孕马血清促性腺激素（ＰＭＳＧ）７．５单位,４８小时后注射人绒毛膜促性激素（ＨＣＧ）７．５单位,于不同时间杀小鼠,取卵母细胞与卵丘细胞的复合体（ＯＣＣ）。从注射ＨＣＧ后到取ＯＣＣ的时间视为卵母细胞的卵龄。将ＯＣＣ置于含８％酒精的Ｍ２中７分钟,再在Ｍ１６中培养５小时后,用０．３ｍｇ／ｍＬ的透明质酸酶去卵丘细胞。卵母细胞形成原核或速即卵裂为激活的标志。将ＯＣＣ加入已获能的精子悬液中,５小时后将从卵丘细胞中释放出来的卵母细胞转移到Ｍ１６中,次日发生卵裂为卵母细胞体外受精和激活的标志。小鼠卵母细胞卵龄为２０ｈ,其激活率为８１．６％,速即卵裂率为４８．０％;而卵龄进一步增加到２４ｈ,激活率和卵裂率转为下降（Ｔａｂｌｅ１）。而卵母细胞受精子激活和受精则不同,卵龄为１５ｈ,卵母细胞的体外受精率为４５．４％;随着卵龄的进一步增加,体外受精率则下降（Ｔａｂｌｅ２）。Ｆｉｇ．１显示：新排出的卵母细胞容易被精子激活而受精;卵龄较大的卵母细胞较易被酒精的人工刺激而激活。可能是卵母细胞从成熟到老化过程中,细胞的结     

Reproduction in the greenback grey mullet, Liza subviridis (Valenciennes, 1836)

This paper presents data on the reproductive biology of Liza subviridis , a little studied mullet species. The fish is heterosexual, exhibiting external fertilization. Six maturity stages can be macroscopically identified in the testes and seven in the ovaries. The macroscopic changes in the gonads are manifestations of histological changes occurring in the development of sperm cells and oocytes. First sexual maturity is attained in the length ranges of 9.5–11.5 cm and 10.5–11.5 cm in male and female fish respectively. The fecundity for fish measuring 10.3–13.9 cm in standard length ranged from 40 000–145 000 eggs. The relationship between fecundity ( F ) and length ( L ) can be represented as: F = 1.9044 L ^4.2998. The spawning duration in L. subviridis is restricted to a short and definite period, with all ripe ova being released within a single spawning act. A pronounced spawning season can be detected to extend from June to November. However, during off-seasons, some spawning also occurs. The correlations between spawning, rainfall and air temperature is discussed.     

Reproductive cycle and sex inversion in razor fish, a protogynous labrid in the southern Mediterranean Sea

The reproductive biology of the Mediterranean razor fish Xyrichthys novacula was investigated by demographic data and histological analysis of the female, intersexual and male gonads. Specimens were collected by bottom trawl on a monthly basis between June 2000 and July 2001 in a sandy bay in southern Thyrrenian. Gonad histology confirmed that the Mediterranean razor fish is a monandric, protogynous hermaphrodite. Females reached first sexual maturity at 100 mm ( L _T) and the estimated mean L _T at first maturity ( L ₅₀) was 125 mm. Females exhibited asynchronous ovarian development and multiple ovulations occurred over the spawning period. Vitellogenesis started in early May and spawning occurred from late May until late September. Sexual transition involved a large‐scale atresia of all oocyte stages and a massive degeneration of ovarian tissue followed by primordial germ cells proliferation. Sex change began at spawning time (June) but transitional individuals tended to cluster at the end of the reproductive period (September). They accounted for 17·1% of the population sampled and were found in a broad size range (105–150 mm L _T).     

Annual changes in the ovarian activity of the freshwater teleost, Barbus luteus (Heckel) from Southern Iraq

The present paper describes the morphology, histology, and annual cyclical changes in the ovaries of Barbus luteus (Heckel). The ovaries are paired structures, joined by short oviducts. The ovarian structure consists of a number of lamellae, which contain the germ cells in various phases of maturation—immature, maturing and mature. Two types of yolk have been reported in the oocyte. The endocrine function of the gonads has been attributed to the follicular cells forming the 'pre-ovulatory corpus luteum' and 'postovulatory corpus luteum'. The ovaries undergo a regular annual cycle which has been divided into five stages, based on various criteria, viz, ovarian size, colour, gonosomatic index, average ova-diameter, histological composition, and the spawning activity.     

Structural characteristics of gonadal development and hermaphroditic phenomenon in freshwater pearl mussel,Sinohyriopisis schlegelii (Hyriopisis schlegelii)

The period of gonads development was first studied from one to five years in the freshwater pearl mussel Hyriopisis schlegelii. It lasted for 36 months and was divided into three main stages: initiation of gonad formation, a stable growth phase, and a reproductive cell development phase. Each reproductive cycle consisted of five stages: proliferative stage (from late January to late February), growth stage (from late February to late March), maturation stage, spawning stage (from early April to late October) and recovery stage (from early November to late January). Interestingly, a hermaphroditic phenomenon was observed in this mussel for the first time, which appears during the development stage from 26 to 32 months. Male and female follicular tissues coexisted in hermaphrodite individuals with the male follicular tissue accounting for more than 90% of the whole gonad tissue. No hermaphroditic phenomenon was observed in matured gonad. We thus speculate that self-fertilization does not exist in H. schlegelii.     

未产卵雌性黄鳝的性转变

为探讨产卵是否为雌性黄鳝(Monopterus albus Zuiew)性转变的必经过程, 研究分析了实验室内从受精卵或幼苗开始养殖至不同时间段的黄鳝性腺组织学状况, 采用性腺活检技术跟踪了34月龄雌性黄鳝性腺发育变化, 并以免疫组织化学方法探讨了黄鳝不同发育状态性腺中增殖细胞核抗原(PCNA)的分布。在养殖过程中, 实验黄鳝没有出现产卵现象或者繁殖行为。在5月龄黄鳝中, 间性占比13.3%, 雄性占比20.0%; 在12月龄(1龄)黄鳝中, 雄性占比17.6%; 34月龄(3龄)黄鳝中, 间性占比12.8%, 雄性占比8.5%。通过性腺活检技术对36条34月龄雌性黄鳝性腺发育变化进行了为期1个月的跟踪研究, 结果表明, 16.7%的雌性黄鳝发生了性转变, 性腺发育到间性阶段。黄鳝间性早期性腺生殖褶增厚, 部分细胞呈现明显PCNA免疫阳性, 包括间质细胞、精原细胞和初级精母细胞。上述结果提示, 产卵并非雌性黄鳝发生性转变的必经过程; 黄鳝性转变初期, 性腺结构变化包括生殖褶中间质细胞和精原细胞的发生和增殖。     

Binding of fluorescent lectins to the surface of germ cells from fetal and early postnatal mouse gonads

Fluorescent lectins were used to study the chemical nature of carbohydrate moieties present on the surface of female and male germ cells isolated from mouse gonads during fetal and early posnatal development. Concanavalin A (ConA), lens culinaris agglutinin (LCA), ricinus communis agglutinin (RCA_I) and wheat germ agglutinin (WGA) bound intensely to the germ cell plasma membrane at all stages studied. Other lectins such as ulex europaeus agglutinin (UEA_I) and agglutinin (SBA) did not bind or bound moderately (SBA to female germ cells only). Distinct developmental-related changes were observed when female germ cells were labeled with fluorescein-conjugated peanut agglutinin (PNA) or dolichos biflorus agglutinin (DBA). DBA and PNA binding was absent or weak in fetal female and male germ cells, but became intensely positive in oocytes in the immediate postnatal period. The percentage of oocytes stained with DBA increased during the first three days after birth, and from day 3–4 onwards all oocytes were strongly labeled. I suggest that these changes in lectin binding reflect changes in biochemical structure of the oocyte surface related to differentiative events occurring in the mouse ovary immediately after birth.     

The reproductive biology of the dab Limanda limanda (L.) in the North Sea: Seasonal changes in the ovary

Oogenesis in the dab is described in six easily identifiable stages: oogonium (Stage I), primary oocyte (II), primary vitellogenesis (III), secondary vitellogenesis (IV), tertiary vitellogenesis (V) and hyaline oocyte (VI). The annual reproductive cycle in female dab may be divided into four morphologically and histologically distinct periods: prespawning (October–January), spawning (February–April), postspawning (May–June) and resting (July–September) period.     

Pigmented Follicle Cells and the Maturation of Oocytes in the Sand Dollar, Dendraster excentricus

Early in the spawning season female D. excentricus can be induced to spawn oocytes in the late stages of oogenesis. Observations with light microscopy indicate that pigment cells migrate in the jelly coat away from the surface of oocytes coincident with the final growth of the oocyte and its maturation. The pigment cells undergo a series of changes in shape and the oocyte elaborates arrays of long microvilli as the cells elevate from the surface of the oocyte. Transmission electron microscopy (TEM) observations of oocytes fixed within the ovary indicate that features of the sequence observed in the spawned oocytes normally take place within the ovary, prior to spawning. Extracts of the pigment cells induce a low level of germinal vesicle breakdown in asteroid oocytes. It is proposed that these cells are homologous to the follicle cells of other echinoderms and are involved in stimulating the maturation of oocytes.     

Reproductive biology ofAwaous guamensis, an amphidromous Hawaiian goby

Synopsis Spawning season, size at first reproduction, oocyte maturation, and fecundity ofAwaous guamensis, an amphidromous Hawaiian goby, were studied from June 1989 through May 1991 in the Wainiha River, Kau'ai, Hawai'i. Female fish larger than 73 mm standard length (SL) had mature gonads from August through December in 1989 and 1990. Gonadosomatic index (GSI) values for mature females ranged from 0.2 to 14.5 during the spawning season. Male fish larger than 64 mm SL had elevated GSI values from June 1989 through December 1989 and from August 1990 through December 1990. Mature sperm were found in two male fish collected in January and February. GSI values for mature males ranged from less than 0.01 to 4.0 in the spawning season. Size-frequency distributions of measurements of vitellogenic oocyte diameters and microscopic observations of oocytes indicated this species has group-synchronous oocyte development. Ovarian maturation stages examined over a 29-month period suggest that members of the stock spawned at different times within the spawning season, although mass spawning events have been documented for this species. Estimates of clutch sizes from nests measured in situ were comparable to estimates of potential fecundity from in vitro examination of ovaries, and indicated that female fish deposited an entire clutch during a spawning event. No evidence for multiple spawning by an individual fish in a single season was found. However, microscopic observations of brown bodies in some ovaries suggested that individual fish probably spawn more than once in a lifetime.