Specific criteria in Grania (Oligochaeta,Enchytraeidae)

The structure of the penial bulb and male efferent duct system of Grania species may be used in addition to setal pattern and spermathecal shape to distinguish species. Six penial bulb types are distinguished: (1) a simple, small, glandular bulb surrounding the male pore; (2) a small, glandular bulb, with a large, associated, dorso-medial gland mass; (3) a small glandular bulb, medial to the male pore, with an elongate male bursa (the aglandular sac), the vas deferens exitting directly into the invaginated male pore; (4) a glandular bulb with an aglandular sac and a small, cuticular stylet embedded in the bulb, extending from the ectal end of the vas deferens; (5) a glandular bulb and an aglandular sac with a long stylet extending from the vas deferens, through the bulb into the sac; and (6) glandular bulb reduced or absent, with or without an aglandular sac; with a long stylet and other prominent modifications, usually muscular, of the vas deferens. The details of the male duct structure were consistent within specimens grouped on the basis of setal distribution and shape and detailed spermathecal structure. Diverse male duct patterns are found within the polytypic species G. macrochaeta and G. postclitellochaeta. The positions of the spermathecal and male pores in their respective segments are distinctive for some species.     

Structure of the male reproductive system of the blue swimmer crab Portunus pelagicus (Decapoda: Portunidae)

An attempt was made here to study the structure of the male reproductive system of Portunus pelagicus, which would improve the knowledge base on the reproductive biology of the species and also help in the maintenance of broodstock under controlled conditions. Male P. pelagicus of different sizes were collected from the Palk Bay off Mandapam (9°17′ N, 79°9′ E) and maintained under controlled conditions for the study. Tissues from testis, anterior vas deferens (AVD), median vas deferens (MVD), posterior vas deferens (PVD), ejaculatory duct and penis were fixed in Bouin's fluid and 2.5% buffered glutaraldehyde separately and processed for light and electron microscopic studies, respectively. The reproductive system consisted of testis, commissure, vas deferens, ejaculatory duct and penis. The vas deferens was divided based on the morphology and/or histology into AVD, MVD and PVD. The AVD was further divided based on histology into proximal and distal regions, and the MVD, based on diameter into major and minor coils. The testicular lobe had several lobules with a central seminiferous tubule, which continued till the penis. The seminiferous tubule was lined by a layer of cuboidal or columnar epithelium. The lining of the central tubule of the vas deferens formed several ‘folds’, which at times formed ‘pouches’. High incidence of cell organelles in the columnar epithelial cells, aggregations of vesicles and occurrence of blebs at the luminal periphery and the projection of numerous microvilli containing electron‐dense materials into the lumen from the cell lining denoted high secretory activity of the epithelial cells.     

Comparative morphology, homologies, and functions of the male system in oribatid mites (Arachnida: Acari)

The penis is basically a double-walled oval cone. The weak type penis (only 2 species) has a weak tongue, lacks a bridge, and is elongate. The strong type (all others) has a bridge, a strong tongue, thicker walls, and is short. An accessory gland and a common vas deferens always open into the inner cup lumen (= ejaculatory duct). The massive tongue muscles may open the penal orifice. A pair of penal retractor muscles originate on the body wall. Penal protrusion and perhaps partial extrusion of stalk substance is by hemolymph pressure. The penis is completely homologous to the ovipositor. The genital discs are cuticular cups containing glandular tissue and are retractible by muscles originating on the body wall. The minute, rod-like, immobile sperm are mixed with seminal fluid and stalk material secreted by seminal vesicle cells. This mixture is carried via the vase deferentia by peristalsis to the penis. Semen and stalk substance (protein) are somehow separated in the ejaculatory duct into separate pools, with stalk substance nearest the penal orifice. Upon penal protrusion, a bit of stalk material is extruded and fastened to the ground, and upon raising of the mite's body the stalk is “drawn out.” Finally, the ball of semen, adhering to the stalk tip, is pulled through the penal orifice.     

Morphology and development of the male reproductive tract in Callinectes danae (Crustacea: Brachyura)

The aim of this study was to characterize the morphology and function of each section of the reproductive system of male Callinectes danae, as well as the stages of reproductive development and their relation to secondary sexual characteristics. Development of their reproductive system begins after completion of the pubertal moult. The growth of the gonopodium showed negative allometry for both juveniles and adults. The reproductive system is divided into portions with different functions. There is a germinal zone in the testes containing spermatogonia, a zone of maturation containing spermatocytes, spermatids or spermatozoa, as well as a collecting duct, which carries spermatozoa to the vas deferens. There are two matrices in the anterior vas deferens that initiate the separation of spermatozoa groups, one composed of polysaccharide acids (matrix I) and another consisting of neutral polysaccharides (matrix II). In the median vas deferens, the matrix II forms an acellular capsule, which forms the spermatophores. In the posterior vas deferens, the matrices are accumulated, initially with a granular texture and are homogenous for the final portion. The ejaculatory duct and penis have muscle lining to expel the spermatophores at copulation. Even after copulation, males retain a stock of spermatophores, allowing copulation with other females.     

Observations on the ultrastructure of the copulatory organ of Archilopsis unipunctata (Fabricius, 1826) (Proseriata,Monocelididae)

The copulatory organ in adult specimens of Archilopsis unipunctata has been studied by transmission electron microscopy.This copulatory organ is of the conjuncta-duplex type with eversible cirrus. The seminal vesicle, lined with a nucleate epithelium, is surrounded by spirally arranged muscles. The fibres are enclosed in a sheath that is continuous with the septum of the bulbus and the basement lamina of the male canal epithelium. Distally to the seminal vesicle the bulbus is filled with the secretory cell-necks of the prostate glands. The male canal shows three different parts: seminal duct, ejaculatory duct and eversible cirrus. At the transition of seminal duct and ejaculatory duct two prostate ducts open into the lumen. The structure of the epithelium lining the different parts of the canal is described. The transition into the cirrus may be recognized by an abrupt change in the thickness, the electron density and the stratification in the basement lamina and by the disappearance of the epithelium absent indeed in the cirrus. The material found inside the cirrus-lumen is different according to the zone considered. The origin of this material and of the cirrus teeth is discussed.Abbreviations ab- apoptotic body - ba- bacteria - bb- basal bodies of cilia - bl- basement lamina - bw- body wall - c- cilia - cb- cell body - cgp- common genital porus - ci- cirrus - cip- cirrus plug - cl- lumen of cirrus - cm- circular muscles - cr- cytoplasmatic remnants - cs- cytoplasmatic sheets - ejd- ejaculatory duct - ep_ej- epithelium of ejaculatory duct - d- desmosomes - f- flagella of spermatozoa - fd- female duct - fp- female porus - gc- golgi complex - gl- glycogen particles - hd- hemidesmosomes - lm- longitudinal muscles - ly- lysosome-like body - m- muscles - m_b- muscles of the bulbus - m_c- muscles of the cirrus - m_c- muscles of the seminal vesicle - mi- mitochondria - ml- microvilli - ms- mesenchyme - n_sd- nuclei of the seminal duct - pd- prostate duct - pg- prostate glands - ri- ribosomes - s- septum - sb- secretory vesicle - sd- seminal duct - sp- spines - sv- seminal vesicle - v- vagina - vd- vas deferens     

Light and electron microscopic studies on the seminal secretions and the vas deferens of the penaeiodean shrimp,Sicyonia ingentis

Unlike the other penaeiodean shrimp, the ridge back shrimp, Sicyoniaingentis does not produce a spermatophore, but transfers sperm suspended in seminal plasm. This paper reports on the histomorphology and ultrastructure of the vas deferens with reference to its functional role in secreting the sperm bearing materials. The vas deferens is divisible into proximal secretory, mid storage and distal ejaculatory regions. The epithelial cells lining the proximal vas deferens are comprised of secretory and absorptive cell types. The loose sperm cells found in the lumen of this region are in an immature condition, and are agglutinated into a compact mass with signs of spermiogenesis in the mid vas deferens. The epithelial cells lining the mid vas deferens are short flattened cells. The distal vas deferens is ensheathed by muscular fibres. The inner epithelial cells are highly secretory and contain numerous microvilli at the luminal end. The sperm cord gets liquefied in this region facilitating the transfer of sperm in liquid form to the female during mating.     

The Vas Deferens of the Spanish Lobster,Scyllarus chacei

Summary

The male reproductive tract of Scyllarus chacei consists of paired testes and vasa deferentia that conduct sperm containing spermatophores to the genital pores at the base of each fifth walking leg. The testis is joined to the vas deferens which can be divided into four regions: (1) the anterior vas deferens can be further divided into three regions. It is highly convoluted and is the region in which the sperm become encapsulated in ovoid spermatophores of approximately 100 sperm as well as produces seminal fluids. (2) The middle vas deferens is the primary site of sperm storage and adds to seminal fluids which formed in the anterior region. (3) The posterior region is highly muscularized and may serve for limited sperm storage. (4) The most distal portion is the ejaculatory duct which is highly muscularized for extruding the spermatophoric mass for transfer to the female. A final seminar product is added here.     

Trichuris odocoileus sp. n. (Nematoda: Trichuridae) from white-tailed deer, Odocoileus virginianus, in southeastern U.S., and a key to trichurids in North American ruminants

A new species of Trichuris from the cecum of white-tailed deer, Odocoileus virginianus, from the southeastern United States, is characterized herein. Males had spicules 2.20 to 3.05 mm long with bluntly rounded tips, an ejaculatory duct equal to or slightly longer than the vas deferens, and a spinous spicular sheath with an expansion near its center. Females had a spinous vulva, usually not everted, a loop in the oviduct just before it opened into the uterus, and a slightly curved posterior portion. Trichuris odocoileus was differentiated from T. lani , a species described in Russia which is most like T. odocoileus, by 1) possessing a spicular sheath with a central expansion, 2) greater size with longer ejaculatory duct and vas deferens, 3) slightly larger eggs, and 4) the unique loop in the oviduct. Trichuris odocoileus constitutes the 6th species of Trichuris recovered from North American ruminants. A key is provided to facilitate differentiation of the six species.     

Internal anatomy and ultrastructure of the male reproductive organization of the Sesarmid crab Muradium tetragonum (1798)—(Decapoda: Brachyura)

Sesarmid crab, Muradium tetragonum, considered a key detritus consumer plays a significant role in the nutrient cycling and energy flow in most of the mangrove environments. Morphological and ultrastructural organization of the M. tetragonum male reproductive system are characterized through transmission electron microscopic studies. Adult males (3.2–4.2 cm) with dark violet carapace and white-tipped cheliped were procured alongside the coastal areas of Tanjavur district, Tamil Nadu, India. The morphological analysis highlights the male gonads to be bilaterally symmetrical and anterolaterally located inside the cephalothorax. A pair of elongated testes lying attached to the hypodermis of the carapace leads to a long highly coiled vas deferens categorized into three distinct regions (Proximal vas deferens, Middle vas deferens and distal vas deferens) structurally and functionally with Posterior vas deferens receiving sac-like accessory glands. It gets followed by an ejaculatory duct and ends with the penile papillae at the coxae's base of the fifth peripod. Structural modifications were observed in the ultrastructure of vas deferens envisage (considering) its functional role in storing spermatophores, active absorption and assisting the secretory activity. Spermatophores, witnessed as spherical bodies are bounded by a dense double wall. Aflagellate, immotile and spherical spermatozoa that measuring 3.6 μm in diameter encompasses a complex acrosome cupped by a nucleus. Moreover, perforatorium and the extending nuclear arms with chromatin, as displayed in the experimental organism M. tetragonum, are in synergy with that of certain brachyurans as specified in the study. Hence, the current study assessing the morphology and ultrastructure parameters of the male gonads could be useful in understanding the physiology of sexual maturation, annual cyclic changes, tracing the phylogenetic relationship among species and enhancing the brood-stock management.     

A new species of Macquaridrilus (Annelida: Clitellata: Naididae) from subantarctic Campbell Island

Macquaridrilus mcmurtrieae n. sp. is described from Campbell Island. This resembles the only other species in the genus, Macquaridrilus bennettae Jamieson, 1968, in most aspects, but shows significant differences in the anatomy of its genitalia. In particular, the spermathecal pores are dorsal rather than lateral, the spermathecae lack diverticulae, the ejaculatory duct is more stout and muscular, the vas deferens is shorter relative to other organs and the anterior prostate is compact rather than elongate. The presence of a cuticular sperm canal appears to be an apomorphy for the genus. The new species was collected from streams and tarns across the island.

http://zoobank.org/urn:lsid:zoobank.org:pub:652AF61D-CFB2-4D07-94C8-59E6FB549D5F

http://zoobank.org/urn:lsid:zoobank.org:act:984F2456-768D-48A1-87AD-4453768BAB8A     

Development of the genital ducts and spermathecae in the Rhyacodrilines rhyacodrilus coccineus and Monopylephorus rubroniveus (Oligochaeta, tubificidae).

The male genital duct in Tubificidae consists of a funnel, a vas deferens, an atrium, and, frequently, a copulatory structure. There may also be a diffuse or compact prostate gland in association with the duct. The morphogenesis of this duct is described for Rhyacodrilus coccineus and Monopylephorus rubroniveus (Rhyacodrilinae). The funnel and vas deferens in both species originate from peritoneal (mesodermal) cells in the posterior septum in the testis segment. The atrium in R. coccineus develops from a primary epidermal (ectodermal) invagination. A typical atrium is not formed in M. rubroniveus; the entire duct is of mesodermal origin. In the latter species, a shallow epidermal invagination occurs, into which both male ducts open, but it bears resemblance to a copulatory structure, which usually forms from a secondary invagination, rather than to a proper atrium. We therefore conclude that M. rubroniveus lacks an atrium. The copulatory structure is termed the male bursa. Both species have diffuse prostate glands that differentiate from peritoneal (mesodermal) cells surrounding the male duct. In R. coccineus the cells cover the atrium, whereas in M. rubroniveus they cover only a part of the vas deferens. The development of the spermathecae and female ducts is also examined. The spermatheca is of ectodermal origin in both studied species, i.e., it forms as an invagination of the epidermis. The female duct develops from peritoneal (mesodermal) cells in the posterior septum of the ovary segment. However, in M. rubroniveus the first sign of the duct disappears and a proper duct never develops.     

中华绒螯蟹(Eriocheir sinensis)雄性生殖系统的组织学研究

中华绒螯蟹雄性生殖系统的组织学研究表明:生精小管一侧为管壁上皮,另一侧为生发区,生殖细胞由生发区基底部同管腔增殖。输精管分为输精细管和贮精囊,管壁上皮具分泌功能,贮精囊有肌肉层。射精管壁肌肉层较厚,粘膜形成纵行皱襞。副性腺内壁为单层立方上皮。生殖系统发育有明显的季节性,8月开始发育加速,10月进入高峰,4月开始发育停滞。     

Morphological changes in eupyrene and apyrene spermatozoa in the reproductive tract of the male butterfly Atrophaneura alcinous Klug

Summary

Eupyrene and apyrene spermatozoa are contained in separate cysts in the testis of the butterfly Atrophaneura alcinous. Spermatozoa of both types from various parts of the male reproductive tract were examined with particular reference to their morphological characteristics. All spermatozoa collected from the vas deferens and the vesicula seminalis were found to be immotile under a dissecting microscope. No spermatozoa of either type were recognized in any part of the ejaculatory duct. Within the testis, eupyrene spermatozoa are present in bundles and each spermatozoon has a slender nucleus with an acrosome and a long flagellum containing mitochondrial derivatives. Two kinds of appendages, lacinate and reticular, are present on the surface of the sperm membrane. They are replaced with an extracellular sheath during passage through the vas deferens. In contrast, apyrene spermatozoa have neither nucleus nor acrosome, whereas a cup-shaped structure was found at the sperm tip instead of the acrosome. Unlike eupyrene spermatozoa, they are surrounded by a concentric sheath outside the sperm membrane in the vas deferens. Individual apyrene spermatozoa and coiled bundles of eupyrene spermatozoa were both found to accumulate in the vesicula seminalis before mating. These morphological changes during passage through the male reproductive tract suggests the occurrence of a kind of maturation and capacitation process reminiscent of mammalian spermatozoa.     

Three New Species of Brevitobrilus (Nematoda) with a Discussion on Relationships within the Genus

Three new species of the genus BrevitobriusTsalolikhin, 1981 are described. Brevitobrilus glandulatus n. sp. is characterized by conspicuous sphincter between pars dilatata and uterus; two pairs of vaginal glands; spicules having elliptical capitula with small proximal stiffening piece; proximally-arcuate gubernaculum; S3 and S4 smaller than other supplements; S6 out of spicular range and 57-60 micropapillae. Brevitobrilus dimorphicus n. sp. is diagnosed by sexual dimorphism in labial sensilla and amphids; thick-walled rectum with a diverticulum protruding into intestinal lumen and males with boat-shaped spicules and S6 occasionally slightly smaller than other supplements. Brevitobrilus allahabadensis n. sp. possesses large amphids of 28-33% of corresponding labial diameter in both sexes; vagina and uterus with muscular, plicate walls; well developed sphincter between vas deferens and ejaculatory duct; capitulate spicules with sloping ventral and angular dorsal walls; S3, S4 and S6 smaller than other supplements, S6 close to cloaca and 28-37 micropapillae. The relationships of the species of genus Brevitobrilus have been assessed using morphological characters subjected to parsimony and a non cladistic key to identification of species is given.     

Two New Genera of Marine Tubificidae (Oligochaeta) from Australia's Great Barrier Reef

Macquaridriloides gen.n. is established for M. heronae from Heron Reef in Queensland, Australia. The species is characterized principally by its lack of spermathecae, and its elaborate male efferent ducts, each of which consists of (1) a ciliated vas deferens, (2) a ciliated and muscular atrium with diffuse prostates, and (3) a stout muscular, non-ciliar ejaculatory duct opening into a large copulatory sac surrounded by posterior prostates. The genus appears closely related to Macquaridrilus Jamieson, 1968, the habitat and zoogeography of which are briefly discussed. Heronidrilus gen.n. is established for H. fastigatus sp.n. and H. bihamis sp.n. both from Heron Reef. This genus is closely related to Macquaridriloides , but the two species differ from M. heronae in that they possess spermathecae and lack ejaculatory ducts.     

Development of the genital ducts in Telmatodrilinae (Tubificidae, Clitellata)

In Tubificidae, the male genital duct comprises a funnel in the testes segment, followed by a vas deferens, an atrium, and, frequently, a copulatory structure in the adjacent ovarian segment. There may also be a diffuse or compact prostate gland in association with the duct. The morphology and position of the genital ducts are important for the classification of the oligochaetous Clitellata. Different parts of the male duct, however, have been named without regard to whether they are homologous or not. One way to establish better hypotheses of homology is to study the detailed morphology and/or the development of the genital ducts. The morphogenesis of the genital ducts in Alexandrovia onegensis (Telmatodrilinae) is described. The male funnel originates by multiplication of peritoneal (mesodermal) cells in the posterior septum in the testes segment. A cord of these cells breaks through the septum and grows backwards into the next segment, where it connects to the epidermis. This cord gives rise to the vas deferens, and is therefore mesodermal in origin. The atrium in A. onegensis develops from a primary epidermal (ectodermal) invagination. The vas deferens and atrium connect and a continuous duct from the testes segment to the exterior is formed. Several compact prostate glands develop along the atrium, each being formed from cells in the atrial epithelium. The spermatheca develops from an invagination of the epidermis in the testes segment. The female duct is formed from peritoneal (mesodermal) cells in the posterior septum in the ovarian segment. These developmental findings strengthen the hypothesis about a closer relationship between the Telmatodrilinae and Tubificinae (both Tubificidae).     

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.     

The spermatozoon of arthropoda. XXIV. Sperm metamorphosis in the diplopod Polyxenus

Specimens, representative of each of the major taxa of mosquitoes, were fixed in copula and the external genitalia examined by scanning electron microscopy. The periphery of the basin-like everted aedeagus of Aedus aegypti precisely matches that of the everted atrial membrane of the female. These structures are appressed during coitus and sealed by pressure of the paraprocts, aedeagal pouch and proctiger. When everted, the aedeagus of male Culex pipiens reveals a ridged dome that surrounds the genital opening. This dome seals itself laterally into a gutter formed by pad-like extensions of the female's genital lips and is sealed dorsally by pressure of the aedeagal apodeme. The aedeagus of another culicine species, Wyeomyia smithii, bears the gonopore at the apex of a spined tube. This tube is inserted between the female's genital lips and is sealed within the genital atrium. The aedeagus of the toxorhynchitine species Toxorhynchitis brevipalpus is immobile and is inserted deep within the genital atrium of the female where it is sealed by pressure of the atrial walls. Males of each of these mosquitoes deliver a mixture of semen and sperm to the copulatory bursa of the female. After withdrawal of the aedeagus, sperm is transferred to the spermathecae. In contrast, sperm of Anopheles quadrimaculatus are delivered directly to the spermathecal duct. The tube-like aedeagus is positioned by its leaflets during sperm transfer and is driven deep into the atrium, where a mixture of semen and sperm is ejaculated. The significance of mechanical barriers to mating between species is discussed.     

Morphogenesis of the Genital Ducts and Spermathecae in Clitellio arenarius, Heterochaeta costata, Tubificoides benedii (Tubificidae) and Stylaria lacustris (Naididae) (Annelida, Oligochaeta)

The development of the male genital ducts in Clitellio arenarius, Tubificoides benedii, Heterochaeta costata (Tubificidae) and Stylaria lacustris (Naididae) is studied with the purpose of investigating the homologies between different parts of the ducts. In both Tubificidae and Naididae, the male duct comprises a funnel, a vas deferens and an atrium. There may also be a prostate gland (diffuse or compact) in association with the duct. The funnel and vas deferens, in all four species, originate from the peritoneal (mesodermal) cells in the posterior septa in the testes segment, whereas the atrium develops from an epidermal (ectodermal) invagination. The prostate glands have different origins in different taxa; in S. lacustris it differentiates from the peritoneal (mesodermal) cells surrounding the atrium, but in H. costata and T. benedii it develops by a multiplication of the atrial (ectodermal) cells; C. arenarius lacks a prostate gland. The development of the spermathecae and the female duct is also studied. The spermatheca is an epidermal invagination. The female duct is of mesodermal origin. However, the position of the duct differs; in S. lacustris the female duct is lateral and the pore is in the ovarian segment, while in the tubificids studied the duct is ventral with the pore in the segment behind the one containing the ovary.     

Mating behavior and genitalic counterparts in tiger beetles (Carabidae: Cicindelinae)

Comparative studies on the structure of genitalia in Pseudoxychila tarsalis Bates and the copulating behavior in 5 species of Cicindela respectively complement similar findings by Freitag [1] on Cicindela spp. and Palmer [4] on P. tarsalis. These strengthen the hypothesis that in tiger beetles the flagellum fits into the spermatheca duct during copulation; that the main function of the flagellum, which is closed at the apex and not connected to the ejaculatory duct, is to open and prepare the lumen of the spermatheca duct for sperm movement from the bursa copulatrix to the spermatheca; and that copulation proceeds in 3 phases: phase 1 in which the lumen of the spermatheca duct is cleared by the flagellum, phase 2 in which the flagellum is withdrawn from the spermatheca duct, and phase 3 in which semen is transferred from the gonopore of the ejaculatory duct to the bursa copulatrix, usually with a spermatophore.