A morphological study of a fish tapeworm, Proteocephalus pollanicola

Parasitology ◽  
1954 ◽  
Vol 44 (1-2) ◽  
pp. 34-49 ◽  
Author(s):  
R. A. R. Gresson ◽  
M. Pauline Corbett

An account is given of the general structure of Proteocephalus pollanicola. The genital system is dealt with in greater detail. The characteristic features of the species are enumerated.The male portion of the reproductive system consists of 60–75 testes in a single layer; vasa efferentia with a lining epithelium; a wide, coiled vas deferens; a small cirrus-sac; a coiled ejaculatory duct and a short cirrus. A description is given of the histological structure of the male ducts.The vagina opens anterior to the cirrus-sac. A well-developed vaginal sphincter is present. The seminal canal communicates with the oviduct and the uterine canal. An oocapt is present; the transverse vitelline ducts and the ovary open into it. A few unicellular glands are present hi the vicinity of the oocapt; these possibly represent Mehlis's gland. An ootype is absent. The histological structure of the female ducts is described.

Parasitology ◽  
1973 ◽  
Vol 67 (3) ◽  
pp. 263-278 ◽  
Author(s):  
R. J. S. Beer

The egg and larval stages of Trichuris suis can be briefly characterized as follows: The egg: barrel shaped, possesses a thick shell consisting of three thick outer layers and an inner thin vitelline membrane, is operculate at each end and is unsegmented and unfertilized when freshly deposited. L. 1 within the egg: presence of an oral spear, a poorly denned oesophagus and an intestinal tract consisting of undifferentiated granulated material. L. 1 within the host: initial differentiation of an oesophagus, cell body, intestine and rectum. L. 2: further differentiation of the body organs and the appearance of the rudiments of the reproductive system. L. 3: initial development of reproductive system and development of a cloaca in the male thus distinguishing the sexes. L. 4: differentiation of reproductive system into vagina, uterus, oviduct and ovary in the female, and testis, vas deferens, ejaculatory duct, spicule and spicular muscle, sheath and tube in the male. L. 5 or adult stage: completed development of the sexual organs including formation of the vulval orifice and eggs in the female and seminal vesicle in the male.


Parasitology ◽  
1922 ◽  
Vol 14 (2) ◽  
pp. 127-166 ◽  
Author(s):  
Sadamu Yokogawa

1. Heligtnosomum muris proved to be very favourable material for the study of nematode development, since it will develop perfectly normally in culture rats, infection is easily carried out and since sexual maturity is reached in 7–10 days after infection.2. The post-embryonal development of H. muris is divided into five stages, two free and three parasitic, with three moults. There is only one moult during free life, the second and third stages being separated by change of habitat brought about by entrance into the host. Sexual maturity is attained soon after the completion of the third moult. The mature worm has two cuticular layers, the outer of which is separated by a space from the inner. This outer cuticula is probably the beginning of a fourth moult which is never completed.3. Under favourable conditions the eggs hatch in about 20 to 24 hours after being passed with the faeces.4. The first two stages of post-embryonal development, which are passed in free life, are separated by a relatively long moult during which the larva changes from the rhabditiform type to the filariform type. During this period there is a rapid division of the cells lining the intestine, which frees masses of these cells into the lumen and leaves the intestine of the filariform larva lined with flattened cells.5. The infective stage is not enclosed in a sheath and tends to work its way out of the culture onto the glass or along the edges of the filter paper. At this stage it is impossible to distinguish the sexes.6. Infection of the rat can be accomplished both by way of the mouth or through the skin although the latter method is by far the most effective. The larvae reach the lungs about 14 to 20 hours after penetration through the skin. They remain in the lungs until about 35 to 65 hours after infection. The majority of them reach the intestine 50 to 65 hours after infection, although in a few they were found as early as 45 hours.7. In the lungs the larvae increase rapidly in size and moult just before they migrate to the intestine. Early in the development in the lungs the sexes can be distinguished by: (1) the migration toward the posterior end of the genital primordium of the female, (2) structural differences in the caudal region, and (3) differences in shape of the genital primordium.8. After reaching the intestine the larvae grow rapidly and enter into the third moult from 96 to 108 hours after infection. In the fourth larval stage between the second and third moults growth and differentiation are most marked. It is during this stage that the differentiation of the organs of the reproductive system occurs.9. Shortly after the completion of the third moult sexual maturity is reached and later the cuticula separates into two layers.10. During the course of development the changes in size and shape and in the character of the cuticula were traced step by step and the differentiation of the digestive and excretory systems were followed as completely as the material would permit. However it was in following the details of the development of the reproductive organs that the investigation was most fully carried out.11. In the male reproductive system the testes, vas deferens, seminal vesicle, cement gland and ejaculatory duct arise by differentiations of the genital primordium and are therefore called internal sex-organs, while the bursa and the spicules which are not developed from the genital primordium are known as the external sex-organs.12. Toward the end of the third larval stage (first parasitic stage) the genital primordium of the male becomes separated into two parts by an extremely delicate strand of tissue. The anterior half of this genital primordium grows forward up to the oesophageal region and forms the testes, the narrow strand connecting the two parts develops into the vas deferens, and the posterior part grows backward to the posterior end, becomes tubular and forms the seminal vesicle, cement gland and ejaculatory duct.13. The bursa is formed from the walls of the posterior end of the male which become very much inflated, and the spicules develop from secretions of a group of spindle-shaped cells which are early differentiated in the posterior region.14. In the development of the female reproductive system the ovary, oviduct, seminal receptacle, uterus and the anterior part of the ovijector arise from the differentiation of the genital primordium and are therefore called internal sex-organs, while the vulva, vagina and posterior part of the ovijector arise from invagination and differentiation of subcuticular cells of the posterior end and are therefore called external reproductive organs.15. After the genital primordium has migrated backward to a position on the ventral side just in front of the anus, it elongates very greatly and grows forward. The anterior part remains as a solid mass of cells and differentiates into the ovary. The rest of the primordium becomes tubular and differentiates into the oviduct, seminal receptacle, uterus and ovijector.16. A group of cells just in front of the rectum and just over the posterior part of the genital primordium increases in number, invaginates, becomes differentiated into a tube which joins with the posterior part of the genital primordium. This tube differentiates into the vulva and vagina. Where it joins the posterior end of the internal reproductive organs there is an overlapping so that the posterior end of the ovijector has a double origin.


2004 ◽  
Vol 35 (3) ◽  
pp. 317-327 ◽  
Author(s):  
Waclaw Wojciechowski ◽  
Karina Wieczorek

AbstractThe structure of the male reproductive system of 14 Chaitophorine species is discussed: Chaitophorus capreae, C. leucomelas, C. nassonovi, C. populeti, C. populialbae, C. salicti, C. salijaponicus niger, C. tremulae, C. truncatus, C. vittelinae, Sipha maydis, Periphyllus aceris, P. coracinus, P. lyropictus. All species, except Sipha maydis, which lives on Poacea (grasses), feed on trees of the families Aceraceae (maples) and Salicaceae (poplars and willows). On the basis of longitudinal sections, cross-sections (paraffin method) and total preparation, the following elements in the structure of the male reproductive system have been examined: the number of testis follicles and the stage of the spermatogenesis; the connection of follicles and vasa deferentia, the position and the histological structure of the wall of vasa deferentia; and the development accessory glands and ejaculatory duct. These characters were then used to supplement morphological data in order to verify the taxonomic position of Chaitophorinae.


1933 ◽  
Vol s2-76 (301) ◽  
pp. 35-61
Author(s):  
DEV RAJ MEHTA

A general account of the internal reproductive organs and the external genitalia and their development is given. The ‘penis lobes’ develop earlier than the ‘valvae lobes’, and independently of them. The tegumen is the modified ninth tergite. The tenth segment is visibly distinguished into a tergal and sternal part in the pupal stages, and the anal tube passes between the two sclerites. The uncus and the gnathos are dorsal and ventral processes respectively of the tenth segment. The anellus lobes develop as lateral processes of the ninth sternite on either side of the penis. The vasa deferentia during larval life do not extend beyond the eighth abdominal segment and lie in a latero-ventral position. They meet the extensions from the ectodermal ‘ductus ejaculatorius duplex’ during the last larval stadium. From the earliest caterpillar stage there exists a pair of ectodermal ducts formed by the differentiation of the epidermis on the ninth sternite. Towards the end of larval life they divide by constriction to form the accessory glands and the ‘ductus ejaculatory duplex’. At this stage they extend on either side to meet the vasa deferentia. The vesiculae seminales develop by distension from the region of junction between the vasa deferentia and the proximal portion of the ejaculatory duct. The ‘ductus ejaculatorius simplex’ arises as an ectodermal invagination between the pair of ‘penis lobes’ during the final larval instar. It is established that, with the exception of the vasa deferentia, all the remaining elements in the efferent genital system are derived from the ectoderm.


Nematology ◽  
2002 ◽  
Vol 4 (8) ◽  
pp. 953-963 ◽  
Author(s):  
Etienne Geraert ◽  
Rita Van Driessche ◽  
Gerrit Karssen ◽  
Wim Bert

AbstractGonads from living young females, representing 23 different species, were extracted to study the cellular structure of the female genital structure within the Meloidogyninae and Heteroderinae. All genera studied can be characterised by their cellular spermatheca morphology. Within Meloidogyne a spherical spermatheca is found with lobe-like protruding cells, most species having 16 to 18 spermatheca cells with interlaced cell boundaries while M. microtyla and M. ichinohei have more spermatheca cells with different cell boundaries. Heterodera and Globodera reveal a comparable gonad structure. The spermatheca cells of Heterodera are columnar and arranged in a restricted number of rows, whereas in Globodera the spermatheca cells are squarish to rounded, depending on the species. The gonad morphology of Afenestrata koreana is clearly different from what would be expected based on the related genera Globodera and Heterodera. The apparently simplest genital system was found in Meloidodera floridensis where the uterus has a limited number of cells. In the other genera studied a large and variable cell number was found.


1937 ◽  
Vol s2-80 (317) ◽  
pp. 99-125
Author(s):  
MARION L. FYFE

The main subject of this paper is a detailed description of the reproductive organs of a planarian initially described by Dendy as Geoplana triangulata. Five unusual features are observed in the reproductive system: 1. The vas deferens consists of a series of wide convoluted branching tubes extending from the region of the mouth to the anterior end of the seminal vesicle. 2. The penis is very small and inconspicuous. 3. The atrium masculinum is provided with three pairs of muscular gland-organs or adenodactyli. 4. The paired ovaries are situated one on each side of the seminal vesicle, not in the region of the brain as is usual. 5. Each ovary is a long fusiform body enclosing more than one true ovary or germarium, as well as specialized parovarian and amoeboid cells which are probably nutritive, and are associated with the internal opening of the oviduct. The writer refers Geoplana triangulata Dendy to the genus Artioposthia owing to the presence of adenodactyli in the atrium masculinum. Each adenodactylus encloses a glandular reservoir from which a ciliated duct leads to the atrial cavity. The actual function of the adenodactyli is obscure, but the very small size of the penis and the fact that the adenodactyli are extrusible suggests the possibility of these latter performing the function of a penis.


1971 ◽  
Vol 49 (4) ◽  
pp. 523-533 ◽  
Author(s):  
G. H. Gerber ◽  
N. S. Church ◽  
J. G. Rempel

The anatomy and histology of the male and female internal genitalia of Lytta nuttalli Say and the functions of the various organs during copulation and oviposition are described. In addition to the ovaries, lateral and common oviducts, and vagina, the female system includes a spermatophoral receptacle, accessory gland, and spermatheca. The most distinctive feature is the voluminous spermatophoral receptacle, which seems to be homologous with the bursa copulatrix of other Coleoptera, but serves to store and digest old spermatophores. The accessory gland is not a colleterial gland, but instead produces materials that probably are involved in the transfer of the spermatozoa into the spermatheca. The epithelia of the calyces and oviducts secrete the frothy, mucilaginous material that coats the eggs at oviposition. In the absence of a separate spermathecal gland, the epithelium of the spermatheca apparently has taken over its functions. The ovaries contain several hundred ovarioles of the telotrophic type. The chief structures of the male system are three pairs of accessory glands plus the testes, vasa deferentia, and ejaculatory duct. Each vas deferens consists of an enlarged portion that serves as an additional accessory gland and a narrow part, which is the seminal vesicle. Materials produced in the three pairs of accessory glands and the glandular portions of the vasa deferentia are used in spermatophore formation. The testes contain several hundred short sperm tubes similar to those of other insects. The arrangement, form, and functions of the internal reproductive organs of L. nuttalli are compared with those of other insects. Observations made on the reproductive systems of four species of Epicauta are also discussed in this context.


Zootaxa ◽  
2011 ◽  
Vol 3096 (1) ◽  
pp. 27 ◽  
Author(s):  
PATRICK C. REYGEL ◽  
WIM R. WILLEMS ◽  
TOM J. ARTOIS

Seven species of eukalyptorhynch flatworms from the Galapagos Islands are reported. Six of them belong to the taxon Koinocystididae Meixner, 1924, three of which are new to science. Two of these new species can be attributed to the genus Itaipusa Marcus, 1949 based on the construction of the prostate vesicle and the general structure of the female system. Itaipusa biglandula n. sp. is characterised by a very short, muscular, unarmed penis papilla, whereas I. renei n. sp. is characterised by the presence of a cirrus armed with minute scales, and two large, blunt hooks in the male atrium. The third new species cannot be placed in any existing taxon and therefore a new genus is erected: Galapagetula annikae n. gen. n. sp.. It is characterised by a straight and rather long cirrus, armed with small spines, and a clearly bipartite bursa in the female system. Additional morphological information is given for the three known species of Koinocystididae: I. divae Marcus, 1949; I. variodentata (Karling, Mack-Fira & Dörjes, 1972) Karling, 1978 and Utelga heinckei (Attems, 1897) Karling, 1954. For I. divae a new locality from Curaçao is also mentioned. The seventh species is a species of Gnathorhynchidae: Prognathorhynchus eurytuba Ax & Armonies, 1987, for which new morphological information on the organisation of the genital system is given.


2018 ◽  
Vol 18 (4) ◽  
Author(s):  
Samantha Alves Seixas ◽  
Norton Dametto ◽  
Eduardo Périco

Abstract: A new species of the genus Temnocephala Blanchard, 1849 from southern Brazil was found on two species of anomuran crustaceans, Aegla spinipalma Bond-Buckup & Buckup, 1994 and Aegla grisella Bond-Buckup & Buckup, 1994, the latter classified as a vulnerable species by the "Lista de Referência da Fauna Ameaçada de Extinção no Rio Grande do Sul. Decreto no 41.672, de 11 junho de 2002". The crustaceans were collected from a tributary creek of the Forqueta river, Perau de Janeiro, Arvorezinha and a tributary creek of the Fão river, Pouso Novo, Rio Grande do Sul, Brazil; both localities belong to the Sub-Basin of Forqueta River. The new species differs from seven other temnocephalans epibionts on Aegla Leach, 1820, by having the following characters: 1. a long and slightly curved cirrus, 2. two vaginal sphincters, one proximal, big and asymmetric, and one distal, smaller and symmetric, and; 3. longer than wide, elongated epidermal 'excretory' syncytial plates (EPs), with a almost horizontally central excretory pore, displaced to the anterior portion of the plate. The new species' EP is the largest in total length among epibionts temnocephalans in crustaceans already registered. Regarding the similarities with the male reproductive system of Temnocephala axenosMonticelli, 1898, the new species has important differences in the female reproductive system. It has a larger proximal vaginal sphincter, located in the middle of the vagina, while the smaller distal one is at the extreme end of the organ. Besides that, the vaginal portion between the proximal and distal sphincters is conspicuous, with a strong muscular wall. This is the first record of a species of Temnocephala in the Taquari Valley, as well in the 'Perau de Janeiro', which is an area with a rich endemic fauna.


Zootaxa ◽  
2018 ◽  
Vol 4433 (3) ◽  
pp. 561
Author(s):  
SEBASTIAN KVIST ◽  
CHRISTER ERSÉUS

Two new species of Tubificoides (subfamily Tubificinae), T. charlotteae n. sp. and T. mackiei n. sp., are described based on morphological analyses. Both species were flagged as potentially cryptic in a previous investigation, based on both mitochondrial and nuclear sequence data. Tubificoides charlotteae n. sp., known only from an intertidal site in southern Spain, is characterized by the lack of cuticular papillation, the possession of several needle-like hair chaetae in dorsal bundles, a cone-shaped penis sheath, and a rather large, muscular penial sac. It strongly resembles the north-west European, largely sublittoral species T. amplivasatus, but differs from this species in terms of body size, width of vas deferens, and the shape and size of both the ejaculatory duct and penial sac. Tubificoides mackiei n. sp., collected from the southeast coast of Norway and the west coast of Sweden, is characterized by the lack of cuticular papillae and hair chaetae, and the possession of a rather long penis sheath with a wide terminal opening. It shares several morphological features with the sympatric species Tubificoides pseudogaster, but is distinguished from the latter by the detailed morphology and length of the penis sheaths, the width of the atrium, and the lower maximal number of bifid chaetae in dorsal preclitellar bundles. The utility of an integrative comparative approach, combining molecules and morphology, for the identification and delineation of new taxa within Tubificoides is briefly discussed. 


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