scholarly journals Positional Relationships among Male Reproductive Organs in Insects

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.

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.


1970 ◽  
Vol 102 (2) ◽  
pp. 144-157 ◽  
Author(s):  
S. N. Mathur ◽  
E. J. LeRoux

AbstractThe anatomy and functions of the male and female reproductive organs of Allothrombium lerouxi Moss are described in detail. In the male, the reproductive organs consist of paired testes, paired vasa diferentia, a median seminal vesicle, a median ejaculatory duct, bursa expulsatoria, a penis, and a median accessory gland; in the female, they consist of paired ovaries, paired oviducts, a median uterus and a vagina. The function of the parts in the male differs from that reported in other species of Trombidiformes, and in females fertilization takes place in the spongy epithelium of the uterus instead of in the oviducts as in oribatids. Females also lack a receptaculum seminis and accessory glands.


2019 ◽  
Author(s):  
Jing Gao ◽  
Guanqun Gao ◽  
Lulu Dai ◽  
Jiaxing Wang ◽  
Hui Chen

Abstract Background Trypophloeus Klimeschi Eggers (Coleoptera: Curculionidae: Scolytinae) is one of the most destructive pests of Populus alba var. pyramidalis (Bunge), resulting in significant losses in economic, ecological and social benefits in China’s northwest shelter forest. But research of reproductive system, spermiogenesis and spermatozoon ultrastructure of T. klimeschi that is basis of phylogeny, reproductive biology and controlling is still black. Results The male reproductive organ of T. klimeschi is composed of testis, seminal vesicle, strand shaped accessory gland containing long branch of strand shaped accessory gland and short branch of strand shaped accessory gland, curly accessory gland, vas deferens and a common ejaculatory duct. The number of sperm per cyst is 350~512. Its spermatozoon is slender, measuring about 75 μm in length and 0.5 μm in wide and composed of a 3-layred acrosomal complex, a nucleus with two different states of aggregation, two mitochondrial derivatives with dark crystal, a 9+9+2 axoneme that run more or less parallel to mitochondrial derivatives, two crystalline accessory bodies with a big compact “puff”-like expansion. Especially in the seminal vesicle, its long flagella folded into several turns and the whole sperm is wrapped in a film.Conclusion The general morphology of male reproductive tract, the spermatogenesis and the spermatozoa of T. klimeschi are, for the most part, similar to the majority of the Curculionidae. However, some distinct differences were found: the low electron-dense band in the cytoplasm of spermatocytes; two different aggregation states of spermatozoon nucleus; especially the stored way of T. klimeschi spermatozoa.


Insects ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 347
Author(s):  
Abdul Hafeez ◽  
Bei Li ◽  
Wen Liu ◽  
Muhammad Nauman Atiq ◽  
Xiao-Ping Wang

Riptortus pedestris (Heteroptera: Alydidae), an important crop pest, is capable of entering reproductive adult diapause under short-day photoperiods. Though the physiological aspects of adult diapause have been well studied in this species, little is known about its morphological development. In the present study, the adult females are discriminated as prediapause and prereproductive based on the absence and presence of mature oocytes in ovarioles, respectively. We also measured the morphological development of vitellarium and lateral oviduct in females, and the accessory gland, ejaculatory duct, and testes in males of both prereproductive and prediapause adults. Our results revealed that there is a clear significant difference in the reproductive development of prediapause and prereproductive insects. Moreover, the internal morphology of reproductive organs was suppressed in prediapausebugs compared to prereproductive bugs, and the insects developedthe reproductive parts as newly emerged adults. The above findings provide basic knowledge on the characterization of diapause and reproductive R. pedestris adults, which would be applicable to molecular investigations.


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.


1932 ◽  
Vol s2-75 (299) ◽  
pp. 467-481
Author(s):  
MARGOT E. METCALFE

1. The genitalia are paired in origin and appear to represent, in the male the coxites and telopodites of the ninth abdominal segment; in the female the telopodites of the eighth, and the coxites and telopodites of the ninth segments. 2. The testes and vasa deferentia, ovaries and oviducts, are paired and mesodermal in origin. 3. The efferent system, other than the testes and vasa deferentia, ovaries and oviducts, is unpaired and ectodermal in origin. 4. The gonopore is serially homologous in the male and female; but is posterior to the ninth segment in the former, and posterior to the eighth segment in the latter. 5. The ejaculatory duct and the median uterus are not strictly homologous, the ejaculatory duct being more comparable with the median accessory gland in the female. 6. There seems to be, in the females of the Insecta, a tendency for the gonopore to be shifted posteriorly.


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.


1994 ◽  
Vol 42 (11) ◽  
pp. 1479-1486 ◽  
Author(s):  
R Tammi ◽  
S Rönkkö ◽  
U M Agren ◽  
M Tammi

To study the expression of hyaluronan in male reproductive organs and the origin of seminal plasma hyaluronan, we stained various parts of the bull reproductive tract for hyaluronan using a biotinylated probe derived from cartilage proteoglycan (bHABC). The potential loss of hyaluronan during tissue processing was checked with a novel technique by blotting frozen tissue sections on nitrocellulose and staining the blots with bHABC. In the same tissues the CD44 receptor was visualized by Hermes 1 antibody. The testes showed only traces of hyaluronan, whereas both the epithelium and the connective tissue of seminal vesicle, prostate, Cowper's gland, and epididymis were positive in bHABC staining. Hyaluronan was localized on the basolateral surfaces of these epithelial cells. The secretions inside the seminal vesicle and in the ducts of prostate and Cowper's gland were HA-positive, whereas the luminal contents of seminiferous tubules and epididymis were unstained both in paraffin sections and in the in situ blocks. The data indicate that hyaluronan in seminal plasma originates from the accessory sex glands. The co-localization of CD44 with hyaluronan in the basolateral surfaces of the accessory gland epithelia and its absence from other epithelia with little or no hyaluronan supports its role as a hyaluronan receptor.


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