Memoirs: The Reproductive System of the Planarian Artioposthia Triangulata (Dendy)

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.

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.


2021 ◽  
Author(s):  
Satoshi Hiroyoshi ◽  
Gadi V.P. Reddy

The location, morphology and function of male internal reproductive organs in insects have been extensively studied, but the relative positioning of those organs is less understood. Position and morphology of the testis, vas deferens, seminal vesicle, accessory gland and ejaculatory duct determine the migration or ejaculation of sperm and other substances. In species where the testis is connected with the seminal vesicle directly or the seminal vesicle is lacking, males usually store complete sperm in the testis and thus can use them immediately for mating. In contrast, the testis of lepidopteran insects is separated from the duplex (sperm storage organ) via the vas deferens, and the sperm are not mature, requiring morphological development in the vas deferens. Here, we discuss the significance of various positional relationships of male reproductive organs and how this relates to their morphology and function with a focus on sperm.


Nematology ◽  
2010 ◽  
Vol 12 (2) ◽  
pp. 255-268 ◽  
Author(s):  
Julia K. Zograf

AbstractAlthough nematodes are a well studied group of multicellular organisms, until now the only information on the cellular structure of the male reproductive system of marine nematodes is that on the histology of free-living marine nematode from the order Enoplida. The fine structure of the male reproductive system of the free-living marine nematode Paracyatholaimus pugettensis (Chromadorida: Cyatholaimidae) from the Sea of Japan has been studied using TEM. The testis epithelium has a large distal tip cell similar to that described for representatives of the subclass Rhabditia. The epithelial wall of the testis is differentiated along its length. The proximal part of the epithelial tube consists of relatively large cells bearing numerous surface outgrowths that permeate between the developing spermatocytes. The epithelium in the middle region of the testis is formed from extremely flattened cells. The distal part of the testis – the seminal vesicle – is filled with immature spermatozoa and consists of absorptive cells. The seminal vesicle is followed by the vas deferens. The gonoduct is also differentiated along its length, the first third being formed from synthetically active epithelial cells, the two layers of which form a tiled structure. There is no lumen in the gonoduct and it is probable that, due to the tiled structure, the epithelial cells move apart to create space for the spermatozoa during ejaculation. The posterior two-thirds of the duct is surrounded by muscle cells that create the necessary pressure during ejaculation. The enlarged epithelial cells of the vas deferens show vigorous synthetic activity, which is probably involved in the transformation of immature spermatozoa into mature gametes.


2001 ◽  
Vol 26 (3) ◽  
pp. 165-174 ◽  
Author(s):  
CN Mowa ◽  
T Iwanaga

We mapped the cellular expression of estrogen receptor (ER) alpha and ERbeta mRNAs in the male reproductive system of the rat during development and adulthood by in situ hybridization. The expression patterns of ERalpha mRNA in the gonad, efferent duct and initial segment of the epididymis during the perinatal period were essentially similar to those of the adult: ERalpha mRNA signals were expressed most intensely in the epithelia of the efferent ducts and initial segment of the epididymis, and in the interstitial cells of the testis from the prenatal period to adulthood. However, ERalpha mRNA signals in the primordial epididymis and vas deferens during the prenatal period were confined to the outermost cellular layer of the ducts, whereas thereafter they were only expressed weakly in the epithelium and stroma of the epididymis and moderately in the muscle layer of the vas deferens. ERbeta signals were expressed intensely (1) in primordial germ and Sertoli cells only during the prenatal period, (2) in arterial walls in the adult testis, and (3) in the epithelium of the sex accessory glands from the perinatal period to adulthood. This report is the first to describe the cellular distribution of ER mRNA in the male reproductive organs during the perinatal period, and complements and confirms earlier data on its distribution in the adult. The broad expression of ERs in male reproductive organs suggests roles for estrogen in regulating tissue development and reproductive events.


1982 ◽  
Vol 60 (6) ◽  
pp. 1172-1183 ◽  
Author(s):  
J. Lai-Fook

The vasa deferentia of Calpodes ethlius are distinguishable into upper and lower regions, each of which consists of expanded and narrower tubular portions. The expanded region of the upper vas deferens is lined by a phagocytic epithelium while the narrower region is lined by a granular secretory epithelium. The expanded region of the lower vas deferens is a true seminal vesicle since it is always full of sperm bundles; it is lined by a nongranular secretory epithelium which extends to the junction with the duplex ejaculatoris. Distinctly different cells occur at the junctions of the three epithelia with each other. The entire vas deferens is surrounded by one or two thin muscle layers.


1994 ◽  
Vol 68 (4) ◽  
pp. 353-358 ◽  
Author(s):  
Y. Takahashi ◽  
C. Goto ◽  
K. K. Kita

AbstractThe ultrastructure of the reproductive system of adult male Trichinella spiralis has been examined, particularly to assist in recent advances such as the localization of target antigens of protective immunity and the mode of immune attack. The male reproductive system consists of a single tube with a hairpin-like bend, composed of a basal lamina, epithelial cells, rachis, circumferential and constrictor muscles, and germinal cells. The organs were surrounded by basal lamina and haemolymph. Germinal cells in different stages of maturation were found on the wall of the testis along its entire length. As the maturation of germinal cells proceeded, the cells moved towards the lumen of the testis. The germinal cells had a row of vesicles (cup-shaped structures) at the cell periphery. The mature sperm, lacking flagella and an acrosome, were stored in the seminal vesicle. The cytoplasm of the epithelial cells of the seminal vesicle and ejaculatory duct was filled with distended rough endoplasmic reticulum (rER) and exocrine granules which appeared homogenous and of medium electron density. The granules appeared to discharge to the lumen.


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.


2021 ◽  
Vol 25 (4) ◽  
pp. 271-276
Author(s):  
U. N. Siakia ◽  
V. Vishwajeet ◽  
R. Kumar ◽  
V. Suri ◽  
K. Joshi ◽  
...  

BACKGROUND: One of the most severe forms of TB, disseminated TB (dTB) is associated with significant mortality. A retrospective study was undertaken to assess the proportion of dTB among inpatient deaths and to describe the pathological spectrum of lesions. Associated comorbidities and missed dTB cases ante-mortem were also sought.METHODS: Data on autopsy-confirmed cases of dTB from over three decades (1988–2016) obtained from the departmental archives of the Post Graduate Institute of Medical Education and Research, Chandigarh, India, were reviewed for clinical details, as well as gross and histopathological findings. The proportion of autopsy-confirmed dTB were reported.RESULTS: During this period, a total of 243 autopsy-confirmed cases were retrieved. The organs most commonly involved in these cases were the lungs (90.1%), followed by the liver (72%), spleen (44%), kidneys (37%), bone marrow (17%), adrenals (12.2%), intestine (11.4%), pancreas (8.5%) and reproductive organs (6.9%). The brain was involved in 73.3% cases. In one third of cases, the diagnosis of TB was not suspected ante-mortem. Comorbid conditions were noted in 36.2% cases.CONCLUSION: A significant burden of dTB was noted among hospital inpatient deaths. Due to multi-organ involvement, dTB has atypical symptoms and may remain undiagnosed ante-mortem. Increased awareness and robust screening of TB cases are mandatory, particularly in patients with underlying comorbidities.


1975 ◽  
Vol 45 (2) ◽  
pp. 225-236
Author(s):  
A.C. Pierrot-Bults

The morphology and histology of the reproductive organs of Sagitta planctonis forma planctonis and of S. planctonis forma zetesios are described. No difference in number of oocytes was observed. The existence of a temporary oviduct is questionable. It may be possible that the so-called accessory fertilization cells are not actually participating in fertilization, but they may have a resorptive or secretory function.


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.


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