刘氏蝎蛉雌性生殖系统的构造

解剖并描述了刘氏蝎蛉Panorpa liui Hua的雌性生殖系统。结果表明,刘氏蝎蛉外生殖器包括下生殖板、内骨,内生殖器官包括卵巢、侧输卵管、中输卵管、附腺、受精囊以及生殖腔。每个卵巢由10~13根多滋式卵巢管组成,12根出现频率最高。     

长足大竹象生殖系统的形态解剖研究

解剖研究了长足大竹象雌雄虫牛殖系统的构造.该虫的雌性生殖系统包括一对卵巢、一对侧输卵管、中输卵管、交配囊、受精囊、生殖腔、产卵器;雄性生殖系统由一对睾九、一对输精管、一对附腺、射精管和交配器组成.     

长蛸生殖系统的形态学与组织学观察

运用解剖学和组织学方法对长蛸(Octopus variabilis)生殖系统的形态结构进行了研究.结果表明,长蛸雌雄异体并异形,雄性右侧第三腕茎化.长蛸雌性生殖系统由一个卵巢、成对的输卵管及输卵管腺组成.卵巢壁上发出一条线状具分支的生殖索,米粒状的滤泡以卵柄连接至生殖索上.每个滤泡是由单层滤泡细胞围绕着一个卵母细胞构成.输卵管形成丰富的纵行褶皱,黏膜上皮具有纤毛.输卵管腺含有两种类型腺细胞.雄性生殖系统包括精巢、输精管前段、储精囊、摄护腺、盲囊、输精管后段和精荚囊.精巢内部被结缔组织分隔成许多精小叶,精原细胞由小叶壁中的生殖上皮产生,并向小叶腔中逐步分化成精子.输精管前段、盲囊和摄护腺所分泌的黏液物质共同参与精荚的形成.储精囊和输精管后段形成较多的纵行褶皱,输精管后段上皮游离面的纤毛可运输生殖细胞.精荚囊的作用则是贮存精荚,囊壁中的平滑肌利于长蛸交配时精荚的排出.     

拟澳洲赤眼蜂生殖系统的研究

拟澳洲赤眼蜂(Trichogramma confusum)的体长约0.6mm,腹部长度约0.3mm.雌蜂生殖系统(包括卵巢、生殖腔、受精囊及三种附腺)位于腹部后端,约占腹腔的2/3.成熟的卵巢由两条多滋式的卵巢管组成.两条成熟卵巢的端段细长,扭卷成一条疏松索,基部膨大,内脏贮存大量卵粒.成对的侧输卵管较短,分别开口于生殖腔后方的两侧,中输卵管缺如.受精囊呈梨形,开口于生殖腔后方.雌性生殖系统三种附腺中,第一种附腺是成对的,呈锤状,分别连接于生殖腔前方两侧;第二种附腺,腺体呈球状,其前端以短曲的小管通进膨大的贮腺囊,贮腺囊端部成柄状的弯曲小管,连接于产卵管的基部开口处.第三种附腺的腺体呈棒状,前端为细长的小管,开口于第二种附腺贮腺囊的前端.雄性生殖系统由成对的睪丸,输精管、贮精囊、附腺及单一的射精管组成.蛹的早期到后期至成虫期睾丸的形态结构,各有不同变化.     

迁粉蝶雌性生殖系统结构研究

解剖和描述了迁粉蝶Catopsilia pomona(Fabricius)的雌性生殖系统结构。结果表明:迁粉蝶外生殖器包括交配囊及其附属结构、导精管、后表皮突和肛突;内生殖器包括1对卵巢、2根侧输卵管、1根中输卵管、受精囊、附腺、外生殖腔及产卵孔。卵巢左右对称,每个卵巢由4根多滋式卵巢管组成。同时提出卵巢发育分级指标,为害虫预测和防治提供指导性意见。     

四种蜡蝉雌性生殖系统比较研究(半翅目,蜡蝉总科)

描述了缘蛾蜡蝉Salurnis marginella(Guérin-Meneville)、八点广翅蜡蝉Ricania speculum(Walker)、斑衣蜡蝉Lycorma delicatula(White)及中华彩象蜡蝉Raivuna sinica(Walker)等4种蜡蝉的雌性生殖系统,并提供了相应的形态特征图。研究结果表明:4种蜡蝉的雌性内生殖系统均为双孔类型;交配管通过阴道与交配囊相连,不直接与交配囊相连;卵巢管为端滋式;阴道、交配囊和受精囊均为双层膜质结构,而卵巢管、侧输卵管则为单层膜质结构。明确了蜡蝉总科昆虫总输卵管与侧输卵管的连接方式,总输卵管为一端固定于阴道内膜,另一端游离于阴道内膜与外膜之间,朝向侧输卵管合并处的透明膜质管状结构。此外,雌性生殖系统中的交配囊、第1产卵瓣、阴道附腺、内生殖突、内生殖瓣等形态特征差异较大。研究标本保存于西北农林科技大学昆虫博物馆。     

斑衣蜡蝉雌性生殖系统超微结构

【目的】明确斑衣蜡蝉Lycorma delicatula雌成虫生殖系统整体形态及超微结构特征,为蜡蝉总科昆虫分类及系统发育探讨提供更多形态学证据。【方法】采用光学显微镜与透射电子显微镜,观察斑衣蜡蝉雌成虫生殖系统整体形态和各主要器官的超微结构。【结果】斑衣蜡蝉雌成虫生殖系统主要包括1对卵巢、1个中输卵管、1个交配囊、1个交配囊管、1个前阴道、1个后阴道、1个受精囊、1个受精管和2根受精囊附腺。卵巢为端滋式,由14根卵巢小管组成,卵室由固有膜、滤泡细胞和卵细胞组成,卵巢小管中的滋养细胞清晰可见;中输卵管位于前阴道基部,由中输卵管腔、上皮细胞、肌肉鞘和基膜组成;交配囊膨大呈圆球状,囊壁由上皮细胞、肌肉层和基膜组成;交配囊管呈圆柱状,连接交配囊和后阴道,由肌肉鞘、上皮细胞层和管腔组成;前、后阴道超微结构相似,主要由肌肉鞘、基膜、上皮细胞和管腔组成,但后阴道上皮细胞细胞核周围存在分泌颗粒,且管腔内有大量微绒毛,而前阴道壁内包含有大量囊泡结构;受精管从中输卵管末端延伸至受精囊,由基膜、厚层肌肉鞘和管腔组成;受精囊为受精管近末端略膨大的囊状结构,由肌肉鞘、基膜、上皮细胞和囊腔构成;雌性受精囊附腺着生于受精囊末端,为均匀的螺旋管状,主要由肌肉层、上皮细胞层和附腺中心管腔组成。【结论】斑衣蜡蝉雌性生殖系统与已报道的蜡蝉总科其他类群的雌性生殖系统结构相似,但卵巢小管数目有差异;蝉亚目中不同总科雌成虫雌性附腺与受精囊附腺的形态特征存在明显区别;斑衣蜡蝉雌性生殖系统超微结构与叶蝉总科和沫蝉总科昆虫也存在部分差异。这些差异是否可以作为头喙亚目高级阶元的划分依据仍有待于进一步研究。     

交配后扶桑绵粉蚧雌成虫卵巢结构及 其他相关结构的变化

利用显微光镜和超微电镜技术观察明确了扶桑绵粉蚧雌成虫卵巢及相关结构的变化,结果表明该虫的内生殖系统含1对卵巢、输卵管、储精囊和1对附腺.每个卵巢有数以百计的端滋式卵巢小管.卵巢小管缺末端纤丝,包含滋养部分和卵黄部分.储精囊表面被丰富的肌原纤维包裹,未经交配的雌虫体内储精囊在显微镜下呈透明状圆形,电镜观察囊内只含液态物质;交配后,储精囊不再维持规则的球状,囊内出现精细胞等物质;精细胞呈典型的“9+2”结构.在初孵化的雌性成虫体内,卵巢小管内的滋养细胞部分中间为营养核,以此联接滋养细胞和卵细胞.卵黄部分包含1个卵细胞.雌性成虫只有通过交配,卵巢内的胚胎才可得以顺利发育;若未经交配,卵巢内的卵细胞将出现发达的内质网结构,标志着细胞将降解而被母体重吸收.     

东方次睾吸虫电镜研究（吸虫纲：后睾科）：Ⅴ.雌性生殖器官

东方次睾吸虫雌性生殖器官（卵巢、输卵管、卵黄－输卵管、卵模、梅氏腺和子宫）透射电镜观察。卵巢内有不同成熟期的生殖细胞,成熟初级卵母细胞有几个靠近核的核仁样小聚体和许多沿质膜的皮质颗粒。首次发现并描述卵巢和输卵管接合处（卵巢壶腹）的超微结构,输卵管上皮为纤毛状,梅氏腺仅一种类型膜状小体细胞,经有微管支持的细小管道穿过卵模将膜状小体排入卵模腔内,在卵黄－输卵管和卵模中有精子,卵模和子宫中有受精卵。虫卵     

橙黄豆粉蝶生殖系统形态学研究

解剖并描述了橙黄豆粉蝶Colias fieldii Ménétriés的生殖系统结构。结果表明:橙黄豆粉蝶雄性内生殖器包括精巢(睾丸)、2个贮精囊、2条输精管、1对复射精管、2根附腺和单射精管。其中2个睾丸体彼此密接似单一器官包被在半透明的睾丸膜中,单射精管较长且分化为形态不同的4段。外生殖器包括抱器瓣、阳茎及其附属结构;雌性内生殖器由1对卵巢、2根侧输卵管、1根中输卵管、肾型受精囊、附腺、外生殖腔及产卵孔组成。卵巢左右对称,每个卵巢具4根多滋式卵巢管。外生殖器包括导精管、囊导管、交配囊及其附属结构、前后表皮突和肛突。     

Ultra- and microstructure of the female reproductive system of Matsucoccus matsumurae

The ultra- and microstructure of the female reproductive system of Matsucoccus matsumurae was studied using light microscopy, scanning and transmission electron microscopy. The results revealed that the female reproductive system of M. matsumurae is composed of a pair of ovaries, a common oviduct, a pair of lateral oviducts, a spermatheca and two pairs of accessory glands. Each ovary is composed of approximately 50 telotrophic ovarioles that are devoid of terminal filaments. Each ovariole is subdivided into an apical tropharium, a vitellarium and a short pedicel connected to a lateral oviduct. The tropharium contains 8–10 trophocytes and two early previtellogenic oocytes termed arrested oocytes. The trophocytes degenerate after egg maturation, and the arrested oocytes are capable of further development. The vitellarium contains 3–6 oocytes of different developmental stages: previtellogenesis, vitellogenesis and choriogenesis. The surface of the vitellarium is rough and composed of a pattern of polygonal reticular formations with a center protuberance. The oocyte possesses numerous yolk spheres and lipid droplets, and is surrounded by a mono-layered follicular epithelium that becomes binucleate at the beginning of vitellogenesis. Accessory nuclei are observed in the peripheral ooplasm during vitellogenesis.     

Sex steroid hormone fluctuations and morphological changes of the reproductive system of the female of Octopus vulgaris throughout the annual cycle

Sex steroids (17beta-estradiol and progesterone) and morphological variations of the reproductive system of the female of Octopus vulgaris from the Bay of Naples were followed over a period of 2 years. The increase in the ovary weight was independent of body weight as demonstrated by the gonado-somatic index (GSI). Both 17beta-estradiol and progesterone have been detected in the ovary of O. vulgaris, and their concentrations changed in correlation with the ovarian development. No 17beta-estradiol or progesterone was found in the hemolymph. 3beta-Hydroxysteroid dehydrogenase activity has been detected in the ovary, indicating that in the female of O. vulgaris the reproductive system is a source of sex steroid hormones. According to the morphological changes of the ovary, the ovarian cycle can be divided into the following phases: previtellogenesis; early vitellogenesis, full vitellogenesis and late vitellogenesis. The morphological changes of the oviducts and oviducal glands throughout the reproductive cycle were in accordance with their role in the transport and secretion of gelatinous coat covering the eggs, as well as in sperm storage and sperm reactivation during fertilization. J. Exp. Zool. 289:33-47, 2001.     

Anatomy of the ovaries of the starfish Asterias rubens (Echinodermata)

Summary The ovaries of the starfish Asterias rubens were studied histologically and ultrastructurally. The reproductive system in female specimens consists of ten separate ovaries, two in each ray. Each ovary is made up of a rachis with lateral primary and secondary folds: the acini maiores and acini minores. The ovarian wall is composed of an outer and an inner part, separated by the genital coelomic sinus. The ovarian lumen contains oocytes in various phases of oogenesis, follicle cells, nurse cells, phagocytosing cells and steroid-synthesizing cells.Oogenesis is divided into four phases: (i) multiplication phase of oogonia, (ii) initial growth phase of oocytes I, (iii) growth phase proper of oocytes I, and (iv) post-growth phase of oocytes I. The granular endoplasmic reticulum and the Golgi complex of the oocytes appear to be involved in yolk formation, while the haemal system, haemal fluid and nurse cells may also be important for vitellogenesis. The haemal system is discussed as most likely being involved in synchronizing the development of the ovaries during the annual reproductive cycle and in inducing, stimulating and regulating the function of the ovaries.Steroid-synthesizing cells are present during vitellogenesis; a correlation between the presence of these cells and vitellogenesis is discussed.     

Evidence of 5-hydroxytryptamine synthesis in the follicles of Sepia officinalis and direct involvement in the control of egg-laying

At the beginning of egg-laying, in the cuttlefish Sepia officinalis, the oocytes accumulated in the proximal oviduct are released into the mantle cavity by the contractions of the oviduct before being encapsulated and fertilised. A bioassay based on the recording of the contractile activity of the distal oviduct was performed to characterise the molecule(s) inhibiting the oviducal motility and then responsible for the storage of the oocytes before mating. From 200 full-grown oocytes, a factor lowering the oviducal contractions was purified and isolated by means of HPLC. ESI-MS as well as electrochemical detection following HPLC fractionation allowed identification of the 5-hydroxytryptamine in the pure fraction. The inhibition of the oviducal contractions by 5-HT was dose dependent with a threshold near 10(-7) M. An immunoenzymatic assay showed that 5-HT appeared in the follicles at the beginning of vitellogenesis and reached a maximum level in the full-grown oocytes. In vitro experiments revealed that 5-HT is synthesised by the follicular cells and the full-grown oocytes, before being released to target proximal oviduct. Thus 5-HT could be one of the molecules involved in the accumulation of oocytes in the oviduct before mating. Mol. Reprod. Dev. 55:182-188, 2000.     

A histological study of the accessory reproductive organs of female Loligo forbesi (Cephalopoda: Loliginidae)

In Loligo forbesi Steenstrup, the female reproductive system consists of the ovary and accessory reproductive organs which include the oviducal gland, the nidamental gland, the accessory nidamental gland and seminal receptacle. Histological studies were made on the accessory reproductive organs of female L. forbesi. The various changes observed during maturation are described and the functional significance discussed. The secretions produced by the oviducal gland and nidamental gland apparently form the egg coats. The seminal receptacle serves to store spermatozoa after mating. The function of the accessory nidamental gland is unknown.     

Seasonal variation in the oviduct of female Agkistrodon piscivorus (Reptilia:Squamata): An ultrastructural investigation

The annual oviductal cycle of the Cottonmouth, Agkistrodon piscivorus, is described using electron microscopy. This is only the second such study on a snake and the first on a viperid species. Specimens were collected in reproductive and nonreproductive condition throughout the year and five ultrastructurally unique regions were recognized: the anterior infundibulum, posterior infundibulum, glandular uterus, nonglandular uterus, and vagina. Except for the anterior infundibulum and vagina, which exhibit no seasonal variation in ultrastructure, the oviduct becomes highly secretory at the start of vitellogenesis. This includes the entire luminal border of the uterus, the tubular glands of the glandular uterus, and the luminal border and sperm storage tubules of the posterior infundibulum. The secretory materials produced in the oviduct vary among regions of the oviduct, and also can vary among time periods in the same region of the oviduct. Variation is especially evident in the sperm storage tubules. Secretory activity in the sperm storage tubules ceases after ovulation, but the tubular glands of the glandular uterus remain secretory until parturition, at which time secretory activity in the varying sections of the oviduct decreases dramatically. After parturition, the oviduct remains in a dormant state until the next reproductive season. The seasonal variation in oviducal morphology mirrors the temperate primitive reproductive cycle known for some pitvipers. Uterine glands of A. piscivorous are more similar in secretory activity to those of an oviparous lizard than a viviparous colubrid snake, suggesting variation in uterine gland morphology between snakes of different families. J. Morphol., 2008. © 2008 Wiley‐Liss, Inc.     

Female reproductive biology of Platygaster diplosisae (Hymenoptera: Platygastridae) and Aprostocetus procerae (Hymenoptera: Eulophidae), two parasitoids associated with the African Rice Gall Midge, Orseolia oryzivora (Diptera: Cecidomyiidae)

We investigated the female reproductive system of Platygaster diplosisae (Hymenoptera: Platygastridae) and Aprostocetus procerae (= Tetrastichus pachydiplosisae) (Hymenoptera: Eulophidae), two parasitoids associated with the African rice gall midge, Orseolia oryzivora (Diptera: Cecidomyiidae). Both optical and electron microscopy were used. The female reproductive system of P. diplosisae includes two large ovaries of the meristic polytrophic‐type, each composed of several tens of ovarioles. The system includes also a venomous gland that extends to a common oviduct. This gland had a filiform secretory portion, in which the epithelium was thin and surrounded a common evacuation canal. The secretory cells secrete into a large reservoir. Parasitism due to P. diplosisae is gregarious. The female reproductive system of A. procerae includes two ovaries of the meristic polytrophic‐type, and each ovary has a few ovarioles. Each ovariole includes one or two oocytes, which can be seen in the vitellarium. Two accessory glands, which extend to the oviduct, are also visible. The secretory epithelium of the accessory gland is made up of a dense network of secretory cells surrounded by muscle fibers. Females of A. procerae pierce the tissues of the gall and probably deposit one egg on or close to the pupa of the midge. Aprostocetus procerae is a solitary parasitoid of the midge. The two parasitoids exploit the same host at different developmental stages. These findings improve our knowledge of the reproductive biology of these two parasitoids associated with the African rice gall midge, an important pest in Africa.     

The ovary structure, previtellogenic and vitellogenic stages in parthenogenetic species Dactylobiotus dispar (Murray, 1907) (Tardigrada: Eutardigrada)

The reproductive system of Dactylobiotus dispar consists of the ovary and the oviduct that opens into the rectum. The sack-like ovary is filled with the developing oocytes, which are assisted by the trophocytes. In D. dispar, the mixed vitellogenesis takes place. One part of the yolk material is produced inside the oocyte (autosynthesis), the second part is absorbed by micropinocytosis while the third part is synthesized in the trophocytes and is transported to the oocytes through the cytoplasmatic bridges. Moreover, rRNA, lipids and mitochondria are transfered from the trophocytes to the oocytes. The histochemical researches show that the reserve material accumulated in the oocytes contains proteins, polysaccharides and lipids.     

A estradiol-17beta receptor in the reproductive system of the female of Octopus vulgaris: characterization and immunolocalization

In this study, for the first time we have identified an estradiol-17beta receptor (ER) in the reproductive system of the female of Octopus vulgaris. Scatchard analysis revealed that one binding component with high affinity and low capacity for the ligand was present in the cytosol, but not in the nuclear extract of the ovary and the oviduct. A steroid specificity competition assay showed that 3H-estradiol-17beta binding activity showed a preference for estradiol-17beta. DNA-cellulose chromatography confirmed the presence of one 3H-estradiol-17beta binding component. By using antibodies anti ER (578-595), we have localized by Western blotting one band of about 70 kDa. ER immunoreactivity has been localized in the nuclei of the follicle cells of the ovary, in the nuclei of the epithelium lining the proximal portion of the oviduct and in the nuclei, and in the cytoplasm of the inner region of the oviducal gland and in the cytoplasm of the outer region of the oviducal gland. These data, taken together, provide evidence that in Octopus vulgaris the ER has biochemical and immunohistochemical characteristics resembling those of ER in vertebrates.     

Morphology of the female reproductive system of European pea crabs (Crustacea,Decapoda, Brachyura,Pinnotheridae)

Commensal pea crabs inhabiting bivalves have a high reproductive output due to the extension andfecundity of the ovary. We studied the underlying morphology of the female reproductive system in the Pinnotheridae Pinnotheres pisum, Pinnotheres pectunculi and Nepinnotheres pinnotheres using light microscopy and transmission electron microscopy (TEM). Eubrachyura have internal fertilization: the paired vaginas enlarge into storage structures, the spermathecae, which are connected to the ovaries by oviducts. Sperm is stored inside the spermathecae until the oocytes are mature. The oocytes are transported by oviducts into the spermathecae where fertilization takes place. In the investigated pinnotherids, the vagina is of the “concave pattern” (sensu Hartnoll 1968 ): musculature is attached alongside flexible parts of the vagina wall that controls the dimension of its lumen. The genital opening is closed by a muscular mobile operculum. The spermatheca can be divided into two distinct regions by function and morphology. The ventral part includes the connection with vagina and oviduct and is regarded as the zone where fertilization takes place. It is lined with cuticle except where the oviduct enters the spermatheca by the “holocrine transfer tissue.” At ovulation, the oocytes have to pass through this multilayered glandular epithelium performing holocrine secretion. The dorsal part of the spermatheca is considered as the main sperm storage area. It is lined by a highly secretory apocrine glandular epithelium. Thus, two different forms of secretion occur in the spermathecae of pinnotherids. The definite role of secretion in sperm storage and fertilization is not yet resolved, but it is notable that structure and function of spermathecal secretion are more complex in pinnotherids, and probably more efficient, than in other brachyuran crabs. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.