粉尘螨生殖系统形态学研究

粉尘螨Dermatophagoides farinae是一种重要的医学螨类。本文用光镜和扫描电镜研究了粉尘螨雌雄生殖系统的形态和结构。结果表明：雄性生殖系统由睾丸、输精管、 附腺、射精管、阳茎及附属交配器官组成。睾丸位于血腔末端,不成对,精原细胞、精母细胞和精子依照精子发育的顺序有规则地分布在其内部。雌性生殖系统包括交配孔、囊导管、储精囊、囊导管、卵巢、输卵管、子宫、产卵管及产卵孔,其中卵巢由一个中央营养细胞和围绕其周围的卵母细胞组成。     

Ultrastructure of the reproductive system of the house dust mitesDermatophagoides farinae andD. pteronyssinus (Acari,Pyroglyphidae) with remarks on spermatogenesis and oogenesis

Several parts of the reproductive system of both sexes ofDermatophagoides farinae andD. pteronyssinus are investigated and compared by light-, scanning electron-, and transmission electron microscopy. New techniques have been employed for scanning of the internal structures of these mites. The male reproductive system consists of unpaired testis, paired vasa deferentia, an accessory gland, ejaculatory duct, and copulatory organ. The female reproductive system consists of bursa copulatrix, ductus bursae, receptaculum seminis, paired ducti receptaculi, ovaries, oviducts, one chorion gland, ovipositor, and oviporus. Testis as well as ovaries are characterized by syncytia of nutritional function. The specifics of spermatogenesis are discussed in connection with sperm transfer. Similarities between the construction of the ovaries and oogenesis in astigmatic mites and telotrophic meroistic ovaries in insects are discussed.     

粉尘螨生殖系统超微结构的透射电镜观察

本研究主要采用透射电镜观察粉尘螨Dermatophagoides farinae (Hughes)生殖系统超微结构。粉尘螨雄性生殖系统是由精巢、 输 精管、 附腺、 射精管、 交配器官及附属交配器官组成。精巢内可同时有精子发育各阶段的细胞。精子无核膜、 核染色质聚集成束、 线 粒体缺乏典型的嵴、 胞质内有平行排列的电子致密薄片等为其特征性结构。雌性生殖系统由交合囊、 交合囊管、 储精囊、 囊导管、 卵 巢、 输卵管、 子宫及产卵管构成。卵巢内可见含多个细胞核的中央细胞, 其周为卵母细胞等生殖细胞。该研究丰富了对粉尘螨生殖系统 结构的认识。     

Internal reproductive organs of the female humpbacked fly,Megaselia scalaris Loew (Diptera : Phoridae)

The female reproductive system of the humpbacked fly Megaselia scalaris Loew (Diptera : Phoridae) was examined in whole mount preparations and serial sections. The system includes 2 ovaries, paired lateral oviducts, a common oviduct, and a genital chamber, opening externally through a gonopore, anteriad and ventrad to the anus. The ducts of the 2 accessory glands open independently into the dorsal region of the genital chamber. The terminal duct of a 2-armed spermatheca joins the right posterior and ventral wall of the genital chamber, immediately inside the gonopore. Passing dorally, the spermathecal duct lies immediately ventral to the duct of the right accessory gland. A short distance posteriad, it divides into two branches, each supplying an arm of the spermatheca. The genital chamber extends both anteriorly and posteriorly from its junction with the common oviduct, creating anterior and posterior compartments. In the right lateral wall of the genital chamber, a distinctive loop-shaped thickening (plate) resembles a darkened thread when it is observed through the integument. Features likely to have taxonomic utility include the posterior and ventral location of the terminal portion of the spermathecal duct; and the asymmetrically arranged, loop-shaped plate.     

The neural control of spermathecal contractions in the locust,Locusta migratoria

The innervation of the spermatheca and demonstration of neural control of spermathecal contractions in Locusta migratoria was illustrated using anterograde and retrograde fills, combined with electrophysiological stimulation and recording. The anterior portion of the spermatheca receives innervation via the receptaculum seminis nerve (N2B2) from two large ventral neurons and one dorsal neuron. All were bilaterally paired and situated in the VIIIth abdominal ganglion. Three ventral bilaterally paired neurons situated in the VIIIth abdominal ganglion also provide innervation to the posterior portion of the spermatheca via the ductus seminalis aperture nerve (N2B3). Six DUM neurons, located in the VIIIth abdominal ganglion, in addition to two centroposteriorly situated DUM neurons in the VIIth abdominal ganglion, are also associated with these two nerves. N2B4 also provides innervation to the posterior portion of the spermatheca. N2B6b is associated with sensory cells identified in the anterior lateral regions of the genital chamber. The spermatheca contracts spontaneously, with peristaltic contractions beginning at the spermathecal sac and continuing along the length of the spermathecal duct. However electrical stimulation of the ventral ovipositor nerve (VON or N2B), receptaculum seminis nerve (N2B2) and the ductus seminalis aperture nerve (N2B3) indicates that contractions are also under neural control. In particular contractions of the spermathecal sac, coil duct and anterior straight duct are initiated via motor projections from the receptaculum seminis nerve (N2B2) and posterior straight duct contractions are controlled by motor input from the ductus seminalis aperture nerve (N2B3). The results suggest that spermathecal contractions of the anterior and posterior portions of the spermatheca are under separate neural control.     

Ultrastructure of receptaculum seminis in Haemaphysalis longicornis (Acari: Ixodidae) in relation to inserted endospermatophore

The receptaculum seminis, opening into the female genital tract, is found only in the metastriate ixodid ticks. An endospermatophore that has been inserted into the female genital aperture at copulation is first stored in the receptaculum seminis, where spermiogenesis is completed before the sperm ascend the oviducts. The receptaculum seminis consists of a simple cuticularized epithelium. Epithelial cells in sexually matured females develop during feeding and become active in secretion. Secretions discharged from epithelial cells are released into the lumen of this organ through the cuticle and may act on the wall of the inserted endospermatophore. The fact that resumption of spermiogenesis (spermateleosis) has already occurred before destruction of the endospermatophore just after copulation suggests that secretions from epithelial cells of the receptaculum seminis are not the trigger of spermateleosis, but a destructive agent of the endospermatophore wall. J Morphol 231:143–147, 1997. © 1997 Wiley-Liss, Inc.     

Ultrastructural investigations of the female genital system of Epiperipatus biolleyi ( Bouvier 1902) (Onychophora,Peripatidae)

Brockmann, C., Mummert, R., Ruhberg, H. and Storch, V. 1999. Ultrastructural investigations of the female genital system of Epiperipatus biolleyi (Bouvier 1902) (Onychophora, Peripatidae). — Acta Zoologica (Stockholm) 80: 339–349. The female genital system of the neotropical peripatid Epiperipatus biolleyi was examined using transmission and scanning electron microscopy. Special attention is given to the two accessory organs of the paired oviducts: the receptacula seminis and the ovarian funnels (Ovarialtrichter). The latter occur only in the Peripatidae, whereas receptacula seminis may also be present in the Peripatopsidae, the only other family in the Onychophora. The ovarian funnels of E. biolleyi are thin-walled and closed from the haemocoel. This trait has also been reported from Epiperipatus trinidadensis, Macroperipatus torquatus, and Eoperipatus weldoni, whereas other peripatids have ovarian funnels which have been reported to open into the haemocoel. The occurrence of artificially opened ovarian funnels, caused by tissue rupture during specimen preparation, is discussed. The presence of spermatozoa both in the receptaculum seminis and in parts of the uterus of the female examined in this study supports the hypothesis that in E. biolleyi insemination of juvenile females occurs directly via the genital opening. The female contained one unstalked cleavage embryo in each uterus horn. Two features of the uterus were found to be unique to E. biolleyi: (1) a second cell layer overlying the uterine epithelium with a pronounced secretory activity (2) embryos are enclosed in a noncellular coat interspersed with numerous transport vesicles.     

Ultrastructural Morphology of the Male and Female Genital Tracts of <Emphasis Type="Italic">Psoroptes</Emphasis> spp. (Acari: Astigmata: Psoroptidae)

The structure of the male and female genital systems of the astigmatid mite Psoroptes ovis (Hering) is described. The male genital system is composed of a paired testis, fused at its proximal part, two vasa deferentia, an ejaculatory duct, into which a single accessory gland opens, and a copulatory organ. The testis is characterized by a peripheric syncytial cell surrounding spermatogonia, spermatocytes, spermatids and spermatozoa which are distributed regularly in the gonad according to the sequence of spermatogenesis. The female genital system consists of a copulatory pore (the bursa copulatrix), a seminal receptacle, paired ovaries and oviducts, a glandular uterus and an ovipositor which leads to the oviporus. Ovaries are composed of somatic cells, germ cells and a central cell, with a multilobular nucleus, connected to oocytes by a stalk. Similarities with other astigmatic mites belonging to Psoroptidia and Acaridia are also discussed.     

Effect of blood meal and mating on the genital tract ultrastructure in the female camel tickHyalomma (Hyalomma) dromedarii (Ixodoidea: Ixodidae)

The genital tract ultrastructure in the femaleHyalomma (Hyalomma) dromedarii is described during feeding and mating and up to oviposition. The vagina, consisting of vestibular (VV) and cervical (CV) regions, is formed of an epithelium lined internally with a folded cuticular layer and surrounded externally by muscle layers. These facilitate the passage of endospermatophores containing sperm into the receptaculum seminis (RS), and ova to the exterior. A pair of tubular accessory glands (AG) opening at the junction of VV and CV consist of an epithelial layer of undifferentiated cells. As feeding progresses, these cells synthesise their granular secretion which lubricates the egg surface during its passage through VV. The RS, opening anteriorly into the CV, consists of cuboidal cells lined with a thin cuticular layer. These cells become rich in glycogen and lipid vacuoles, possibly acting as a source of energy for various cell activities including granule synthesis and exocytosis. The granules discharge their contents into intercellular spaces distributed throughout the RS wall and communicate with the main lumen via narrow channels. The cell secretion may dissolve the endospermatophore wall to release sperm, while their lysosome-like structures may function in the breakdown of endospermatophoric material taken up by pinocytosis. The connecting tube (CT) opens into the CV anterodorsally and leads into the common oviduct (COV) posteriorly. It consists of an epithelium lined by a closely-adhering cuticular layer, giving the tube lumen the appearance of an undulate labyrinth with a complicated configuration. No secretory activity in the CT has been observed before, during, or after feeding. The paired, non-cuticular oviducts, extending from the ovary and fusing anteriorly to form COV, consist of an epithelium poor in cell organelles. At the final stages of feeding the cell cytoplasm contains large, phagosomal vacuoles penetrated by sperms, in addition to micropinocytotic vesicles which serve to break down the seminal fluid and other materials. The basal membrane is infolded giving characteristic features, which increase dramatically during oviposition, of epithelia involved in ion and water transport. The oviducal secretion may function as a tanning agent to harden the egg-shell and may also act as a lubricant for egg passage.     

Ultrastructure of the salivary glands of the planthopper,peregrinus maidis (ashmead) (Homoptera : Delphacidae)

The principal salivary gland of the planthopper, Peregrinus maidis (Ashmead) (Homoptera : Delphacidae), comprises 8 acini of only 6 ultrastructurally different acinar types. In these acini, secretory cells contain elongated vacuoles partly lined by microvilli and by microtubule bundles. These vacuoles are apparently connected with extracellular canaliculi deeply invaginated into secretory cells. Canaliculi of each acinus lead to a ductule lumen, which is lined with spiral cuticular intima, surrounded by duct cells. Striated muscle fibers, supplied with small nerve axons and tracheoles, are found in various acini of the principal gland, usually around secretory and duct cells.In the accessory salivary gland, the 2 large secretory cells contain no elongated vacuoles or canaliculi invaginations. However, in their central region, apically, these cells border a large microvilli-lined canal with its own canal cells. This canal is apparently connected with the cuticle-lined accessory duct, formed by duct cells. Nerve axons, but no muscle fibers, are found in the accessory gland and its duct. It is suggested that the system for transporting secretory material within acini of the principal gland, is basically different from that within the accessory gland.     

Ultrastructural organization of the genital tracts in amphigonic females of Euceraphis betulae Koch (Aphididae: Calaphidinae)

The ultrastructure of the genital tracts in amphigonic females of Aphidoidea is described for the first time, using Euceraphis betulae Koch (Aphididae: Calaphidinae) as a representative. The female reproductive apparatus consists of two ovaries, each one with three/four meroistic telotrophic ovarioles; two sac‐like accessory glands lie laterally to a sac‐like seminal receptacle, opening into the dorso‐medial part of the common oviduct by means of a spermathecal duct. A marked secretory activity takes place in the epithelial cells of all the investigated tracts as shown by ultrastructural observation of many organelles involved in this process. No evident golgian area was observed in the cytoplasm of these cells. Extensive smooth endoplasmic reticulum, whose probable role is here discussed, was observed in epithelial cells of the wall of the accessory gland. Spermathecal duct and seminal receptacle had peculiar features that could be related to different secretory activities carried out by these two parts of the spermatheca.     

Mechanisms of sperm release from the receptaculum seminis of Schistocerca vaga Scudder (Orthoptera: Acrididae)

Release of spermatozoa from the receptaculum seminis of Schistocerca vaga was studied by means of electrical and mechanical stimulation. Electrical stimulation of the receptaculum nerve, or the ductus aperture nerve, leads to release of spermatozoa from the receptaculum seminis, provided the spermathecal innervation is intact. Mechanical stimulation of the ductus aperture in the genital chamber also leads to sperm release, provided the neural loop, ductus aperture/terminal abdominal ganglion/receptaculum seminis, has not been interrupted at any point. Ten somata in the terminal abdominal ganglion, including 6 dorsal unpaired medial (DUM) neurons, innervate the receptaculum seminis; some of these somata may be neurosecretory. Approximately 80 presumed sensory axons run from the ductus aperture to the same ganglion. On the basis of these neuroanatomical data and the results of electrical and mechanical stimulation, a schema of how the release mechanisms operate in S. vaga is proposed.     

Ultrastructure of the Accessory Glands in Female Genitalia of Pholcus phalangioides(Fuesslin, 1775) (Pholcidae; Araneae)

Pholcus phalangioidesdoes not possess receptacular seminis. The uterus externus (genital cavity) itself functions as a sperm storage structure. Two accessory glands are situated in the dorsal part of the uterus externus; they discharge their secretory product into the genital cavity. The secretion is considered to serve primarily as a matrix for sperm storage, i.e. to keep the spermatozoa in a fixed position. The accessory glands consist of numerous glandular units, each being composed of four cells: two secretory cells are always joined and surrounded twice by an inner and an outer envelope cell. Both envelope cells take part in forming a cuticular ductule that leads from the secretory cells to the pore plates of the uterus externus. The inner envelope cell produces the proximal part of the canal close to the microvilli of the secretory cells, whereas the outer envelope cell produces the distal part of the canal leading to the pore plate. Close to the pore the latter exhibits prominent microvilli that might indicate additional secretory activity.     

Ultrastruktur-Untersuchungen am männlichen Genitaltrakt und an Spermien vonTetranychus urticae (Tetranychidae,Acari)

Zusammenfassung Die paarigen Hoden vonTetranychus urticae sind wie die anderer prostigmater Milben in einen Keimteil und einen Drüsenteil, der ein weites Lumen (Hodenlumen) enthält, gegliedert. Der Drüsenteil ist schlauchförmig und geht in eine anfangs paarige, dann unpaarige Vesicula seminalis über. DerTetranychus- Penis besteht aus zwei verschiedenen Teilen: einer Ausstülpung der Körperwand, die vom Ductus ejaculatorius durchzogen wird, und einer ventral davon gelegenen kutikularen Einstülpung, an deren proximalem Ende Penisprotraktoren ansetzen.Eine Beschreibung der Feinstruktur der einzelnen Elemente des männlichen Genitaltraktes sowie des Receptaculum seminis des Weibchens wird gegeben.Der Keimteil des Hodens wird aufgebaut von einer vielkernigen somatischen Zelle, die die Keimzellen umgibt. Die Spermiocytogenese ist durch folgende Vorgänge gekennzeichnet: Einfaltung der Zellmembran, Degeneration von Zellorganellen, Größenabnahme und Kondensation von Kern und Cytoplasma. Kinocilie und Akrosomkomplex werden nicht ausgebildet. Die Spermien verlassen den Keimteil als kugelige Gebilde, die abgeschnürten Einstülpungen liegen als periphere Vesikel unter der Zellmembran. Das Chromatin ist kugelförmig zusammengeballt, eine Kernhülle ist nicht vorhanden. Mitochondrien, Golgi-Apparat und Ribosomen sind verschwunden.Im Receptaculum seminis bekommen die Spermien eine unregelmäßige Gestalt mit fingerförmigen Ausläufern. Unter der Zellmembran und parallel zu ihr liegen zahlreiche Tubuli.

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Ultrastructural investigations on the male genital tract and sperms ofTetranychus urticae (Tetranychidae, Acari)

Summary The paired testes of the spider miteTetranychus urticae are divided in a part producing germ cells and a secretory portion with a vast lumen. The secretory part is tubular and is connected to a vesicula seminalis that begins with paired pieces and then becomes unpaired. The penis is composed of two different parts: an evagination of the body wall that is penetrated by the ejaculatory duct and a ventral cuticular invagination the proximal part of which is an insertion for protractor muscles.The ultrastructures of the male genital tract and of the receptaculum seminis of the female are described in detail.The germinal epithelium is built up of a multinuclear somatic cell which envelops the germ cells. The spermiogenesis is characterized by the following features: invagination of the plasma membrane, degeneration of cell organelles, reduction in size and condensation of nucleus and cytoplasm. The germ cells lack flagellum and aerosome. The sperms leave the germ producing part of the testis with roundish shape, the invaginations — now pinched off the cell membrane — are to be seen as peripherally located vesicles. The chromatin is condensed, a nuclear envelope is absent. Mitochondria, a Golgi apparatus and ribosomes are reduced.In the receptaculum seminis the sperms are of irregular shape, they bear finger-shaped processes. Below the cell membrane numerous tubules are to be found.

     

Fine structure of the spermatheca and of the accessory glands in Orchesella villosa (Collembola, Hexapoda)

The spermatheca and the accessory glands of the collembolan Orchesella villosa are described for the first time. Both organs exhibit ultrastructural differences, according to the time of the intermolt in which the specimens were observed. A thick cuticular layer lines the epithelial cells of the accessory glands. In the reproductive phase, they are involved in secretory activity; a moderately dense secretion found in the apical cell region opens into the gland lumen. Cells with an extracellular cistern are intermingled with the secretory cells. These cells could be involved in fluid secretion, with the secretory product opening into the cistern which is filled with an electron-transparent material. After the reproductive phase, the gland lumen becomes filled with a dense secretion. The accessory gland secretion may play a protective role towards the eggs. The spermatheca is located between the accessory glands; its epithelium is lined by a thin cuticle forming spine-like projections into the lumen and consists of cells provided with an extracellular cistern. Secretory cells, similar to those seen in the accessory glands, are missing. Cells with a cistern could be involved in the production of a fluid secretion determining sperm unrolling and sperm motility.     

The fate of the normal-anucleated spermatozoa in inseminated females of the silkworm Bombyx mori

Both typical (haploid) and atypical (anucleated) spermatozoa reach the receptaculum seminis of inseminated females of Bombyx mori intermingled. However, only typical spermatozoa both leave the receptaculum and fertilize the eggs. Atypical spermatozoa, which are in fact anucleated flagellar apparatuses, probably function in transporting typical fertilizing spermatozoa to the receptaculum seminis. In the male ejaculatory duct both kinds of spermatozoa are wrapped with extra-cellular sleeves that presumably protect them on their way to the receptaculum. Typical spermatozoa “hatch” from the sleeves before leaving the receptaculum to fertilize the eggs. The presence of a centriole in the extra-testicular spermatozoa of this species supports the generalization that insect spermatozoa do have a centriole at the base of the flagellum.     

Ultrastructure of the accessory gland in the parthenogenetic thrips heliothrips haemorrhoidalis (Bouché) (Thysanoptera : Thripidae)

The fine structure of the reproductive accessory gland of the parthenogenetic thrips Heliothrips haemorrhoidalis (Thysanoptera : Thripidae) is reported. It consists of an apical bulb and a fine gland duct. The former consists of an epithelium with secretory and duct-forming cells surrounding a large gland lumen lined with a thin cuticle and filled with dense secretion. Spent secretory cells degenerate and are eliminated from the epithelium. The gland duct is characterized by an irregular, branched lumen surrounded by a very flat epithelium. A valve controls the opening of the duct lumen. The proximal gland duct runs through a cuticular papilla that opens between the dorsal ovipositor valves. The secretions may serve for ovipositor valve lubrication and possibly to protect laid eggs. Observations of serial sections through the vagina exclude the presence of a spermatheca in this species.     

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。