Ultrastructure of the Z-organ and Parts of the Female Genital Tract in Xiphinema coxi coxi

Ultrastructure of the Z-organ and associated apophyses in Xiphinema coxi coxi was studied by transmission electron microscopy to determine their structural origin and relationship with other parts of the genital tract. The Z-organ of X. coxi coxi is oval-shaped, ca. 30 µm long and 16 µm wide. It is clearly distinguished from the other parts of the female genital tract by its thick muscular outer wall, epithelium-lined lumen, and 4-5 centrally located apophyses. Each apophysis is continuous with the epithelial lining of the Z-organ, suggesting that it originated from epithelium. The apophyses appear as thickened and densely folded masses forming numerous interlaced pores and (or) chambers containing mucous-like materials and electron-dense crystals. These apophyses are characteristic of a typical Z-organ; no globular structures characteristics of the pseudo-Z-organ were observed. The thickness of the muscular layer of the oviduct and uterus varied with position. The overall Z-organ ultrastructure of this study, including body wall and internal apophyses, was comparable to the typical Z-organ of X. ifacolum. This suggests that X. coxi coxi should be classified as a Xiphinema species that contains the typical Z-organ.     

On the structure of the Z pseudo-organ in Xiphinema diversicaudatum

The structure of the Z pseudo-organ in Xiphinema diversicaudatum consists of a muscular mass of about 80 cells arranged in rings of four cells each. These cells have peripheral nuclei and are connected with a glandular monolayered epithelium, which lines the lumen of the Z pseudo-organ. Globular bodies originate from the membranes of the epithelial tissue. They consist of a series of closed vesicles containing secretions, and of tubules through which the secretions flow into the lumen. The globular bodies have a helicoidal distribution within the lumen of the Z pseudo-organ which presumably slows the passage of the egg. Enzymatic digestion, in vivo, indicates that the secretion consists of acid and basic proteins involved in egg shell formation.     

Vesicle involvement in the egg cortical reaction of the horseshoe crab,Limulus polyphemus L

Ultrastructural observations (TEM) of the cortical reaction in Limulus polyphemus have been difficult to obtain due to the relative impermeability of the transparent egg envelope to standard fixatives. With the application of trialdehyde fixation techniques [Kalt, M. R., and Tandler, B. (1971). J. Ultrastruct. Res.36, 633–645], the cortical reaction has now been examined and the role of cortical vesicles has been determined. The size of these vesicles in uninseminated eggs is heterogeneous, with small vesicles (0.5 μm) being apposed to the plasmalemma and with large vesicles (4 μm) located in a lower layer of the egg cortex. The contents of the small vesicles are translucent under the electron beam. With the onset of egg activation these vesicles fuse with the overlying plasmalemma. The contents of the large vesicles appear electron dense and exhibit distinctly different morphologies. Shortly after insemination these large vesicles begin to enlarge by fusing together. By 9 min after insemination some enlarged vesicles fuse with the plasmalemma to form pits on the egg surface. The remaining enlarged vesicles continue to fuse with the plasmalemma until approximately 60 min after insemination when few vesicles are remaining.     

The surface ultrastructure of the egg capsule of Transversotrema patialense (Transversotrematidae: Digenea)

Bundy D. A. P. 1981. The surface ultrastructure of the egg capsule of Transversotrema patialense (Transversotrematidae : Digenea). International Journal for Parasitology11: 19–22. Scanning and transmission electron micrographs show that the egg capsule of the digenean Transversotrema patialense bears thread-like extensions 3 μm long and 0.12 μm in diameter at a density of one per μm^?2. These extensions trap bacteria and detritus against the egg capsule surface. The ultrastructural topography of the egg capsules of this species differs from the forms previously described for other parasitic platyhelminths. It is suggested that the capsular sculpturing arises as an incidental consequence of moulding effects at the egg capsule-reproductive tract interface during ovogenesis.     

Egg sac silk of Theridiosoma gemmosum (Araneae: Theridiosomatidae)

Cocoons of Theridiosoma gemmosum consist of two main parts, the egg sac case and the stalk. The inner space of the egg sac case is filled with nonsticky flocculent silk. Measuring 600–800 nm in diameter, the flocculent threads are never made up of bundles of longitudinally oriented nanofibrils. The egg case wall consists of a lower layer of highly ordered threads and an upper layer of cover silk. The lower, permanently white layer consists of threads in a mesh‐like arrangement, the thicker threads being 4–6 μm and the thinner threads being 2–3 μm in diameter. Each thread is a bundle of parallel nanofibrils, with a diameter between 150 and 300 nm. The silk secretions of these fibers, emitted from spigots, are processed by legs. The upper layer of the egg case is applied to the threads of the lower layer by direct rubbing against its surface, i.e. without the use of legs. In the lower and middle part of the egg case, the accumulated secretion forms a virtually compact encrustation, whereas in the upper, conically shaped, part of the egg case where it becomes the stalk, this secretion becomes substantially scarcer. The stalk is a continuation of the egg case, its proximal part made of fibers similar to those forming the inner layer of the egg case wall. The distal part of the stalk continues towards the suspension area either as a compact bundle of parallel fibers, or the stalk forks into two bundles of roughly the same thickness, which continue towards the suspension area separately. On the surface of objects onto which cocoons are attached, the secretion of the piriform glands acts as an adhesive sheet. J. Morphol. 2009. © 2009 Wiley‐Liss, Inc.     

Fine structure of the genital system in the females of Pergamasus mites (Acari: Gamasida: Pergamasidae)

The female reproductive system in Pergamasus mites consists of an unpaired vagina, vaginal duct, uterus, and ovary. Additionally, there are paired vaginal glands, as well as unpaired ventral and paired lateromedial glandular complexes. The vagina and vaginal duct are cuticle‐lined. In the dorsal wall of the vagina, this lining forms the endogynium which possesses a “sac” and two conspicuous “spherules” and is armed with “stipula” and other cuticular protrusions. The endogynium functions as a spermatheca, being a storing site for the spermatophore. The spherule procuticle is perforated by microvilli of underlying cells that are structurally very unusual. The lining of the vaginal duct forms numerous cuticular fibers directed toward the vagina. There is an external layer of muscles, supposedly functioning as a sphincter. The uterus is an organ in which the fertilized egg is stored for some time and starts embryonic development. Its wall is composed of glandular epithelial cells. The ovary consists of inner and outer parts. The former part is formed by a nutritive syncytium, whereas the latter contains growing oocytes. Two groups of glands connect with the genital tract. Paired vaginal glands are composed of glandular and secretion‐storing parts and open into the vagina. Paired lateromedial and unpaired ventral glandular complexes empty into the genital tract between the vaginal duct and uterus. The structure of the female genital system is discussed in terms of its function and phylogeny. J. Morphol. 240:195–223, 1999. © 1999 Wiley‐Liss, Inc.     

The structure of the egg-shell of Porrocaecum ensicaudatum (Nematoda: Ascaridida)

Wharton D. A. 1979. The structure of the egg-shell of Porrocaecum enslcaudatum (Nematoda: Ascaridida). International Journal for Parasltology9: 127–131. The egg-shell of Porrocaecum ensicaudatum is oval with an opercular plug at either end. The shell consists of three layers: an inner lipid layer, a middle chitinous layer and an outer vitelline layer. The vitelline layer has strands of particulate material attached to its outer surface. The chitinous layer consists of 8.5 nrn fibrils which are made up of a chitin microfibril core surrounded by a protein coat. The fibrils are oriented randomly or in parallel, there being no indication of helicoidal architecture.The chitinous layer varies in thickness to form a pattern of interconnecting ridges on the surface of the egg. This pattern presumably increases the shell's structural strength.     

Xiphinema llanosum and Trophurus vultus, Two New Plant Nematode Species from Pasture Soils in Colombia

Xiphinema llanosum n. sp. and Trophurus vultus n. sp. are described and illustrated from grass soils in Llanos Orientales, Colombia. Xiphinema llanosum is a bisexual species. The female body length is 2.3-2.7 mm, odontostyle 86-96 μm, and odontophore 58-65 μm long; vulva at 42-47%; anterior ovary is absent; the anterior uterus and oviduct are similar to the posterior branch but slightly reduced; and the tail is dorsally convex-conoid with a blunt hemispherical terminus. Male body length is 2.06-2.96 mm; spicules are 40-44 μm long; and four (rarely three or five) anterior ventromedian supplementary papillae are present. Trophurus vultus females are 0.52-0.67 mm long; vulva at 56-60%; stylet is 10.5-13.5 μm long; isthmus is as long as the basal esophageal bulb; the tail is subclavate, 1.6-2.2 times anal body width long; and the terminal cuticle thickness is about one-sixth of the tail length.     

Observations on egg production in the monogenean Entobdella soleae

Egg production in the monogenean Entobdella soleae increases as adult parasites grow. Medium-sized adults (anterior hamulus length 550–600 μm; total body length approx. 5 mm) produced about 30 eggs per day at 12°C. Parasites with anterior hamuli exceeding 650 μm in length (total body length about 6 mm) may produce more than 60 eggs per day. In smaller adults, eggs tend to spend longer in the ootype after assembly of the shell and the ootype remains empty for longer periods of time. The time taken to assemble a single egg is relatively constant (4–6 min) in adults of all sizes and there is evidence of a small but significant increase in egg size as parasites increase in size. Some eggs were retained in the uterus for as long as 168 min but others spent less than 5 s in the uterus, indicating that the uterus is no more than a passageway for these eggs to the outside world. The egg cell (or zygote) precedes the vitelline cells as they progress along the ovo-vitelline duct to the ootype.     

Blastodermic cuticles of a springtail,Tomocerus ishibashii Yosii (Collembola : Tomoceridae)

The formation and structure of the blastodermic cuticles of a springtail, Tomocerus ishibashii Yosii (Collembola : Tomoceridae) are described together with the change of egg membrane. The blastodermic cuticles of the Collembola are 2-layered, and formed in the early stages of the embryonic development, preceding the differentiation of germ band. The first blastodermic cuticle is thicker (about 0.8-1.5 μm in thickness) and its surface is provided with complex structures, whereas the second one is thinner (about 0.2-0.4 μm in thickness) and smooth. About 3 days after oviposition, the chorion (about 2 μm in thickness) splits into 2 and the first blastodermic cuticle, provided with many projections and 4 large spines appear on the surface of the egg. Three types of projections are distinguished: button-, cone- and seta-like structures. The halves of the ruptured chorion are attached to the first blastodermic cuticle on both sides below the spines, and no projections are found in the regions concealed by the ruptured chorion. The projections of the first blastodermic cuticle are formed by cellular protrusions of the blastoderm. The conspicuous large spines on the first blastodermic cuticle are formed by the evaginations of the blastoderm. Tendrils of the primary dorsal organ run between the first and second blastodermic cuticles.     

Unusual membranous network with spines in the uterus of Xiphinema coomansi (Nematoda: Longidoridae)

An ultrastructural study of the uterus of Xiphinema coomansi reveal that the numerous uterine spines present in this species are not anchored to the inner wall of the tubular uterus, but are symmetrically arranged and attached in a membranous network suspended throughout the entire length of the uterus. The spines are solid, hexagonal structures enveloped and connected in tri-radial fashion to each other, as well as to the inner uterine wall by a continuous thin undulating membrane. The network membrane thus formed encloses numerous compartments on the luminal side of the uterus, which seems to create a type of barrier between the plicated uterine wall and a rather constricted central lumen. No such membranous intrauterine network has been reported previously in the reproductive system of nematodes.     

Apical end organ structure and histochemistry in plerocercoids of Proteocephalus ambloplitis

The end organ of Proteocephalus ambloplitis pleroceroids was studied by light microscopy and histochemistry. The end organ consists of a spherical sac filled with an amorphous, granular secretory product. The lining of the end organ is devoid of an epithelial cell layer. Protease was detected within the end organ by a gelatin-silver film technique. No aminopeptidase activity was detected. The end organ was PAS positive and diastase-fast. A positive test was obtained for neutral mucopolysaccharides and protein. The end organ is thought to assist migration of larvae through host tissue.     

Ultrastructural studies on the nematode Xiphinema diversicaudatum: Egg shell formation

The ultrastructure of the formation of the egg shell in the longidorid nematode Xiphinema diversicaudatum is described. Upon fertilization a vitelline membrane, which constitutes the vitelline layer of the egg shell, is formed. The chitinous layer is secreted in the perivitelline space, between the vitelline layer and the egg cell membrane. On completion of the chitinous layer, the material of the lipid layer is extruded from the egg cytoplasm to the outer surface, through finger-like projections. Both chitinous and lipid layers are secreted by granules in the egg cytoplasm that disappear as the layers are completed. Chitinous and lipid layers are formed during the passage of the egg through the oviduct. The vitelline layer is enriched with secretions produced by the oviduct cells and then by phospholipids secreted by the cells of the pars dilatata oviductus. The inner uterine layer is also formed by deposition of secretory products apposed on the egg shell in the distal uterine region and Z-differentiation. In the proximal part of the uterus, the egg has a discontinuous electron-dense layer, the external uterine layer. Tangential sections between chitinous and uterine layers revealed the presence of holes, possibly egg pores, delimited by the two uterine layers.     

Eggshell fine structure of three lepidopteran pests: Cydia pomonella (L.) (Tortricidae), Heliothis virescens (Fabr.), and Spodoptera littoralis (Boisd.) (Noctuidae)

The eggshells of 3 moths, Cydia pomonella (Tortricidae), Heliothis virescens, and Spodoptera littoralis (Noctuidae) were investigated by scanning (SEM) and transmission (TEM) electron microscopy. The surface of the noctuid eggs shows structural elements (micropylar rosette, ribs, cross-ribs, and aeropyles) and regional differentiation, all typical of Lepidoptera. The egg of C. pomonella shows a different regional morphology due to its watch-glass shape and its position, lying on the flank. The micropylar structures are on the lower egg face in contact with the substrate. For S. littoralis, the surface structure (sculpturing) of the egg is not species-specific, being indistinguishable from that of S. frugiperda (Salkeld, 1984).In all 3 moths, the eggshell fine structure is basically identical, as revealed by TEM. Both the vitelline envelope and the chorion consist of several distinct layers. The vitelline envelope, bi-layered and several μm thick, undergoes a marked structural change when embryogenesis begins. At the same time, Golgi vesicles bearing dense particles, appear in the periplasm of the egg cell in fertilized eggs of H. virescens and S. littoralis. The chorion of all 3 species consists of a basal layer (C-1), a cavity layer (C-2) supported by trabecles and opening to the exterior via aeropylar canals, and a lamellar layer (C-3), which probably consists of helicoidally arranged stacks of fibrils. In H. virescens and S. littoralis, an additional epicuticle-like layer (C-4) is present. Available data from the literature are summarized and a basic scheme of the radial eggshell fine structure of ditrysian Lepidoptera is proposed.     

Morphology and function of reproductive organs in Neodasys chaetonotoideus (Gastrotricha: Neodasys) with a phylogenetic assessment of the reproductive system in Gastrotricha

The reproductive system of the important basal gastrotrich Neodasys chaetonotoideus is described and reconstructed on the basis of light microscopy, serial ultrathin sections (ultrastructure) and scanning electron microscopy. Starting frontally, the hermaphroditic reproductive system consists of paired and tube shaped lateral testes that do not possess elongated seminal ducts but most likely open directly via paired ventral pores. The unpaired, medio‐dorsal ovary region contains early oogenic stages that mature caudally towards the uterus region, where the most mature egg is positioned laterally to the midgut. The ovary region is not covered with an epithelial lining whereas the uterus region possesses a distinct epithelial wall. Between ovary and uterus region, we have detected a conspicuous section of the female gonad, the vitellogenic oviduct that consists of a thick epithelial wall which forms cellular protuberances into the developing oocytes passing the oviduct. We interpret this as a special, hitherto undescribed mode of vitellogenesis in Gastrotricha. Further caudally, the uterus continues with the fronto‐caudal organ, a complex of two substructures that are apparently homologous to the frontal organ and the caudal organ of many species of the Gastrotricha Macrodasyida. Neodasys chaetonotoideus obviously engages in spermatophore formation and transfer. In this study we develop a morpho‐functional scenario for the gonads and accessory organs in terms of spermatophore production, exchange and oviposition. We compare our newly obtained data with already published results on the reproductive organs of several species of Gastrotricha by means of a species‐character matrix and provide a computer aided evaluation by a parsimonious character optimization. A reconstruction of the reproductive system of the stem species of Gastrotricha on the basis of three recent phylogenetic analyses is presented. These reconstructions give support for a Neodasys‐like reproductive system in the ground pattern of Gastrotricha with slight morphological differences and direct transfer of spermatozoa rather than spermatophore transfer. The evolution of selected characters is traced thus revealing some incidents of convergent evolution as well as the evolutionary replacement of the ancestral frontal organ by the derived frontal sac in at least two separated lineages.     

Morphology,fine structure,and functional aspects of the labial gland reservoirs of the subterranean termite Reticulitermes santonensis de Feytaud (Isoptera: Rhinotermitidae)

The morphology and fine structure of the labial gland reservoirs in the subterranean termite Reticulitermes santonensis (Isoptera: Rhinotermitidae) was studied by light and transmission electron microscopy. The reservoir wall consists of a single epithelial cell layer and a cuticular intima. The reservoir ducts are formed by a flat epithelial matrix with cuticular ridges lining the duct lumen. Measurements of the ionic concentrations of reservoir fluids and haemolymph show that the osmolality of reservoir fluid ranges from 7 to 28 mosmol kg⁻¹; the haemolymph osmotic pressure was 201 ± 31 mosmol kg⁻. The reservoir lumen is effectively separated from the haemolymph compartment; a net water flow through the reservoir wall could not be induced in physiological experiments. Moreover, typical epithelial structures associated with a fluid transport against an osmotic gradient are lacking. Thus, our fine structural and physiological data support the view that a water transfer from the haemolymph through the reservoir wall into the reservoir lumen does not occur.     

Ultrastructure of sperm cells in the female gonoduct of Xiphinema

The ultrastructure of the sperm cells in the female gonoduct of the nematodes Xiphinema theresiae and X. pinoides is described. The nucleus of the sperm cells is composed of several electron-dense clumps of chromatin that is not surrounded by a nuclear envelope. A layer of mitochondria, in which the mitochondrial cristae are only rarely visible, lies around the nuclear material. In the surrounding cytoplasm packets of electron-dense fibres are abundant. The sperm in the uterus have the following surface differentiations: highly intertwined protrusions between adjacent sperm cells, protrusions coinciding with the plication of the inner uterine wall and a slightly undulated surface towards the uterine lumen. It is argued that in the uterus, the sperm cells actively move in proximal direction by a mechanism resembling pseudopodial movement, in which the packets of fibres are involved. In the oviduct, the sperm cells loose their surface protrusions and the packets of fibres gradually become less abundant. Since the oviduct has no pre-formed lumen, the sperm cells appear to wedge their way along by forcing oviduct cells apart.     

Purification and properties of bovine myocardial phosphorylase phosphatase (protein phosphatase C).

Phosphorylase phosphatase was purified to homogeneity from bovine myocardium by the procedure of Brandt et al. (Brandt, H., Capulong, Z. L., and Lee, E. Y. C., (1975) J. Biol. Chem.250, 8038–8044). The purified enzyme consists of a single polypeptide chain of M_r, 34,800 as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The K_m for phosphorylase a was 2.9 μm and at V_max, the enzyme had a turnover number of 11.7 mol phosphorylase a (dimer) converted/mol phosphatase/s. Phosphorylated histone and protamine were also substrates for this phosphatase. The K_m for histone was 46 μm (based on incorporated ³²P_i and at V_max a turnover number of 3.3 mol phosphate released/mol phosphatase/s was found. In general, the properties of the bovine phosphorylase phosphatase closely resemble those found for the rabbit liver enzyme.     

Ultrastructure of the Anterior Body Region of Marine Nematode Deontostoma californicum

The ultrastructure of the anterior body region of the free-living marine nematode Deontostoma calilornicum was studied by electron microscopy. The body wall consists of a nine-layered cuticle, a cellular hypodermis containing eight nerve bundles, and a well-developed coelomyarian somatic musculature. Nerves in the dorsal, lateral, ventral, and submedian hypodermal chords anterior to the nerve ring were observed with regularity. Structure of subventral somatic setae suggests a mechanoreceptive function. The esophagus is cellular and consists of three marginal cells alternating with an equal number of radial muscle cells, three esophageal glands, and three enteric nerves. The membranes of adjacent esophageal cells are sinuous. Apices of the triradiate lumen are connected with the outer wall of each marginal cell by bands of electron-dense nonmyofibrils, whereas two types of myofilaments run radially between the apophyses of the lumen and the outer walls of radial cells. Each myofibril, which forms hemidesmosomes at both ends, is interpreted to be the morphological equivalent of one sarcomere. Synaptic junctions between the processes of muscles, gland cells, and axons of the enteric nerves are described in detail.     

Developing embryo and cyclic changes in the uterus of Peripatus (Macroperipatus) acacioi (Onychophora,Peripatidae)

Female reproductive tracts of the viviparous neo-tropical onychophoran Peripatus acacioi have been examined at different times throughout the year, and the altering relationship between the developing embryo and the uterus is described. Depending on her age and time of year, the female may have one or two generations of embryos within her uterus. The uterine wall consists of a thin outer epithelium and basal lamina, three layers of muscles, and a thick basal lamina beneath an inner epithelium lining the uterus lumen. These layers are consistent along the length of the uterus apart from the inner epithelial lining, which varies according to position in the uterus and the developmental stage of embryos contained in the uterus. Early embryos are positioned along the length of the uterus and therefore have space in which to grow. During cleavage and segment formation, each embryo is contained within a fluid-filled embryo cavity that increases in size as the embryo grows. Morulae and blastulae are separated by lengths of empty uterus in which the epithelial lining appears vacuolated. Until the process of segment formation is complete, the embryos are attached to a placenta by a stalk and remain in the same part of the upper region of the uterus. As these embryos grow, the lengths of vacuolated cell-lined uterus between them decrease. Each embryo cavity is surrounded by the epithelial sac, the maternal uterine epithelium, which becomes overlaid by a thin layer of cells, the embryo sac, which is believed to be of embryonic origin. The placenta is a syncytial modification of the epithelial sac located at the ovarian end of each embryo cavity covered by the embryo sac and is analogous to the mammalian noninvasive epitheliochorial placenta. Segment-forming embryos have their heads directed toward the ovary. As the embryo gets longer during segment formation, its posture changes from coiled to flexed. Once segment formation is complete, the embryo loses contact with its stalk, an embryonic cuticle forms, and the embryo turns around so that its head is directed toward the vagina. The embryo escapes from its embryo sac and moves to the lower part of the uterus. In the lower part of the uterus, the straightened fetuses are first unpigmented but subsequently become pigmented as the secondary papillae on the body surface form and an adult-type cuticle forms beneath the embryonic cuticle. While the embryos are contained within their embryo cavities, nutrients are supplied by the placenta. Throughout development the mouth is open and in the mature fetus the gut is lined by peritrophic membrane and material is present in the gut lumen. Trachea have been observed only in fetuses that were ready for birth. Insemination, cyclical changes in the uterine epithelium, and the nature of the cuticle shed at parturition are discussed. © 1995 Wiley-Liss, Inc.