The anatomy, histology, and physiology of the reproductive systems of Lytta nuttalli Say (Coleoptera: Meloidae). I. The internal genitalia

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.

1978 ◽  
Vol 56 (12) ◽  
pp. 2542-2553 ◽  
Author(s):  
G. H. Gerber ◽  
G. B. Neill ◽  
P. H. Westdal

The anatomy and histology of the female and male internal reproductive organs of the sunflower beetle, Zygogramma exclamationis (F.), are described. The female system consists of a vagina, bursa copulatrix, common oviduct, lateral oviducts, spermatheca, spermathecal accessory gland, and ovaries. Twelve ovaries examined contained from 23 to 32 telotrophic ovarioles, the average being 27.3. The male system consists of a pair of bilobed testes, a pair of accessory glands, vasa deferentia, and an ejaculatory duct which is bifurcated at its anterior end. Three testes examined contained 34, 36, and 37 sperm tubes, respectively. The basic features of the reproductive systems of Z. exclamationis are similar to those of other Chrysomelidae.


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.


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.


2021 ◽  
pp. 1-17
Author(s):  
Imelda Martinez-M. ◽  
Sara L. Rivera-Gasperín ◽  
Hortensia Carrillo-Ruiz ◽  
Miguel A. Morón

The anatomy of the internal male reproductive systems of 12 species of Melolonthinae (Phyllophaga, Chlaenobia, Macrodactylus, Isonychus), six species of Dynastinae (Cyclocephala), and three species of Rutelinae (Paranomala) (Coleoptera, Scarabaeoidea) of Mexico are described. A total of 350 male specimens representing 21 species were collected. From each species, the reproductive systems were obtained by micro-dissection, placed in a liquid fixative, stained, and drawn to scale. The internal genitalia of each species was described and compared among the species examined. The reproductive system of the Melolonthinae species is comprised of two testicles, each with six follicles, two deferent ducts, two accessory glands, two glandular ducts, an ejaculatory duct, and the aedeagus (not described for any of the species examined). The number of testicular follicles per testicle is as reported in different species of other Scarabaeoidea subfamilies. The length of the accessory glands and the ejaculatory duct varies in the species studied. The ejaculatory bulb is present in all of the species of Dynastinae and Rutelinae examined but in only three species of Melolonthinae.


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.


1984 ◽  
Vol 15 (2) ◽  
pp. 151-178 ◽  
Author(s):  
Niels P. Kristensen

AbstractThe genital segments and internal genitalia of Agathiphaga vitiensis are described. Sternum VIII is anteriorly produced into blunt paired apophyses and posteriorly into a tongue-shaped lobe. Segment IX is a complete ring, very short in the dorsal and ventral midlines; its anterolateral lobes are largely apodemal. The long and curved gonopod ("valva") consists of a single piece. There is no median sclerite between the gonopod bases, but an open, softwalled "subgenital crypt" below the entrance of the phallocrypt may be homologous with the "median plate" in other primitive homoneurous moths. Tergum X bears a pair of broad "superior lobes" and the postgenital complex terminates in a medially intended, sclerotized "terminal lobe" above the eversible perianal area. The roof of the posterior part of the genital chamber bears a median aggregation of cuticular spines (the "spiny plate"), and a pair of smooth lateral sclerotizations ("presocii") tentatively attributed to venter X: a pair of setose sclerites (socii) are tentatively attributed to the paraprocts. The area bearing the spiny plate and presocii may in repose be folded down behind the phallus, thereby closing the phallocrypt. The phallus comprises a tubular phallotheca and an eversible aedeagus; the thick basal margen of the phallotheca is posteriorly expanded and forms the floor of the greater part of the phallocrypt; there is no ventral aedeagal branch. The musculature comprises two IX/X muscles, a segment IX muscle inserting on the subgenital crypt, phallic pro- and retractors (the former originating in the gonopod), intrinsic phallic muscles, a single segment IX muscle (adductor) to the gonopod and five intrinsic muscles of the postgenital complex. Each testis comprises four large, separate follicles. The spermatozoa do not remain grouped in discrete bundles in the vas deferens. Seminal vesicles are located on the vasa deferentia close to the testis and are doubtfully homologous with the vesicles in other Lepidoptera. The unpaired ejaculatory duct is very short. The evidence bearing on a reconstruction of the ground plan of the lepidopteran male genitalia is reviewed. Segment VIII was similar to the preceding segments. It is tentatively suggested that tergum and sternum IX were fused, that the gonopod was undivided and that a tubular, partly sclerotized aedeagus was present; deviations from these states within the order are therefore considered to be autapomorphic. The base of the aedeagus was probably surrounded by a short, collarlike phallotheca. It is suggested that there was a median sclerite between the gonopod bases, but the presence of discrete, paired and muscular "valvellae" in the lepidopteran ground plan is considered doubtful. It is further suggested that dorsum X bore a pair of lobes and that there were paired sclerotizations in venter X. The X/XI boundary is very difficult to trace. Seventeen muscle sets are ascribed to the lepidopteran ground plan; it is considered an autapomorphy of this ground plan that the phallic protractor originates within the gonopod. The testes presumably had large, separate follicles and there may have been two pairs of tubular accessory glands. The testes and the double set of accessory glands of Agathiphaga could be cited in support of a sistergroup relationship to all other Lepidoptera whereas the phallic structure (and possibly the "spiny plate") might support a sister group relationship to the Heterobathmiina. There is no support in male genital structure for a sistergroup relationship to the Heterobathmiina + Glossata; the latter phylogenetic hypothesis may be preferable on other grounds, however.


1928 ◽  
Vol s2-72 (287) ◽  
pp. 447-483
Author(s):  
C. J. GEORGE

1. In the male Philaenus and Agrion the vasa deferentia terminate on the ninth segment in the early stages. An ectodermal invagination from that segment joins them subsequently and thus the male gonopore is established. 2. The accessory glands develop in Philaenus male from the anterior end of the swollen extremities of the vasa deferentia and the vesiculae seminales from a still more forward region. 3. The accessory glands of the male are mesodermal in origin and not ectodermal as some authors state. 4. There is no evidence as to the existence of a ‘pair of ectodermal ejaculatory’ ducts either in Philaenus orin Agrion, and reasons are adduced to show that they do not exist at all in the higher Insecta. 5. In the female nymph of Philaenus the oviducts terminate on the seventh segment. They are subsequently joined by an ectodermal invagination from the seventh segment. The common oviduct is formed in two parts: the anterior part is derived from the posterior region of the invagination on the seventh and the posterior region is formed as a groove from the ectodermis of the eighth segment and subsequently this groove is converted into a tube. When the second part is completed it is in connexion with the invagination from the seventh and opens to the outside on the eighth segment. The ectodermal invagination from the seventh also gives rise to the spermatheca. A median accessory gland develops as an invagination from the ninth segment between the bases of the inner ovipositor lobes. A pair of accessory glands develop as paired imaginations from the anterior region of the ninth segment. 6. In the female nymph of Agrion the oviducts fuse to form a single duct and terminate in the middle of the eighth segment. Posteriorly an ectodermal invagination from the eighth segment meets this duct and lies in a position dorsal to it. Later on the ectodermal invagination develops a spermatheca dorsally and the mesodermal and the ectodermal ducts unite into one. The accessory glands develop as paired ectodermal invaginations from the anterior region of the ninth segment. 7. The female gonopore is not homologous in the different groups of insects. The vaginal opening in Orthoptera, Hymenoptera, Homoptera, Diptera, and Lepidoptera is homologous. The vaginal opening in Coleoptera is homologous with the oviducal opening of Lepidoptera, with the opening of the accessory gland of Homoptera, Hymenoptera, Diptera, Isoptera, and the opening of the spermatheca in some Orthoptera. 8. The common oviduct, being formed differently in the different groups is not homologous. The accessory organs, e. g. spermatheca, are not homologous in the different groups. 9. There is no evidence to show that the common oviduct is of paired origin. 10. The occurrence of a median accessory structure on the ninth segment which develops in the young as an invagination between the bases of the inner ovipositor lobes is very general in the higher Insecta. In some it functions as a gland, in others as a storehouse for spermatozoa. 11. The homology of the paired accessory glands is indicated. 12. The male genital ducts are not strictly homologous with those of the female. The homologue of the ejaculatory duct is the invagination from the ninth segment in the female. 13. The Odonata stand isolated in having a mesodermal region for the common oviduct and in the peculiar development of the two processes between the anterior ovipositor lobes. 14. The probable lines of evolution of the female efferent system in Insecta are indicated. The study of the development of the female efferent system indicates that the groups Orthoptera, Homoptera, Lepidoptera, and Diptera are very closely allied. Coleoptera seem to have had quite a different line of evolution from the above groups in this respect. 15. The adult Odonatan anatomy of the genital organs in the female as observed by me is in some respects different from that described by Tillyard. In conclusion I wish to express my deep sense of gratitude towards Professor Balfour-Browne and Dr. J. W. Munroe, both of whom have always been ready to help me. My colleague Mr. R. I. Nel, who is working on similar lines in this department,, has rendered me valuable help, not only in matters connected with the subject proper but also in translating difficult German references. I am also indebted to Mr. Peter Gray who helped me a good deal in translating references in Italian.


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.


1976 ◽  
Vol 54 (6) ◽  
pp. 990-1002 ◽  
Author(s):  
G. H. Gerber

The histogenic changes in the internal genitalia and mesenteron and the hardening and darkening of the cuticle during the first days of adult life in Tenebrio molitor L. are described. At emergence, the testes contain mature spermatozoa and the ovaries possess small oocytes. During the first 3 days, the shape, size, appearance, and staining characteristics of the secretory cells of the lateral oviducts, female accessory gland, tube accessory glands, bean-shaped accessory glands, and glandular region of the vasa deferentia change. Similar changes were not seen in the seminal vesicles and spermatheca. All of the secondary sex glands are filled with secretion by day 4. In the midgut, changes occur in the size, shape, and appearance of the epithelial cells by the 3rd day, and a peritrophic membrane is secreted during days 2 and 3. Most adults do not begin to feed until after the 3rd day. By day 3, the hardening and darkening of the cuticle are completed. All of these changes clearly are associated with adult maturation, especially sexual maturation, and most or all of the them must take place before the adults are able to copulate and oviposit.


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.


Sign in / Sign up

Export Citation Format

Share Document