Internal female reproductive anatomy and genital interactions during copula in the yellow dung fly, Scathophaga stercoraria (Diptera: Scathophagidae)

1999 ◽  
Vol 77 (12) ◽  
pp. 1975-1983 ◽  
Author(s):  
D J Hosken ◽  
E P Meyer ◽  
P I Ward

Insect genitalia have been extensively studied for taxonomic purposes, but functional anatomy has rarely been examined. We report here on the detailed internal anatomy of the reproductive tract of female yellow dung flies (Scathophaga stercoraria) and the mechanics of copula and sperm transfer. Female dung flies have paired accessory glands, three spermathecae (one singlet and one doublet), each with its own narrow duct, a large muscular bursa copulatrix, which is met by the common oviduct dorso-anteriorly, and paired lateral oviducts and ovaries. The bursa is lined internally with a thick cuticle. During copula and while ejaculating, the male aligns the gonopore with the spermathecal duct entrances to the bursa and pinches the female's abdomen at approximately this point. Sperm packing in the spermathecae appears quite orderly, and structurally the sperm appear typical of many insects. Aedeagus withdrawal appears to remove some bursal sperm. The results are discussed in relation to other Diptera.

2021 ◽  
Vol 5 ◽  
pp. 95-100
Author(s):  
Karin Thüler ◽  
Wolf U. Blanckenhorn ◽  
Paul I. Ward ◽  
Stefan Lüpold ◽  
Luc F. Bussière

Female and male reproductive traits co-evolve through pre- and post-copulatory sexual selection and sexual conflict. Although males typically transfer many sperm during copulation, only a small proportion reach the fertilization site because females often actively or passively reduce sperm number in their reproductive tract. Males may transfer accessory substances to protect their ejaculates against female selective processes, which benefits males but can harm females. In turn, females may use accessory gland fluids to control paternity or sperm storage. Female yellow dung flies (Scathophaga stercoraria) have paired accessory glands that produce fluids involved in fertilization and egg laying. One proposed function for these fluids is spermicide. Alternatively, female accessory gland fluid may help keep sperm alive to avoid fertilization failure or encourage sperm competition. Using yellow dung flies, we investigated the interaction of female accessory gland fluid with sperm in vitro. Significantly more sperm remained alive when exposed to accessory gland fluid compared to buffer only (63% vs. 44%). We conclude that female accessory gland fluid in yellow dung flies can help nourish rather than kill male sperm, although selective nourishment of sperm is as consistent with cryptic female choice as is selective spermicide.


Reproduction ◽  
2008 ◽  
Vol 136 (5) ◽  
pp. 657-665 ◽  
Author(s):  
A Nation ◽  
S Cui ◽  
L Selwood

Ovarian-based immunological research is currently restricted to proteins of the zona pellucida. This study examined the immunocontraceptive potential of a novel vesicle-associated protein, VAP1, previously isolated from the vesicle-rich hemisphere of the brushtail possum oocyte. Seven female possums were immunized against recombinant glutathione S-transferase-VAP1 fusion protein. Control animals (n=3) received antigen-free vaccinations. Following immunization, regular blood sampling determined the level and duration of immune response. Animals were monitored daily, pre- and post-immunization, to determine estrous cycling activity and the percentage of reproductive cycles yielding viable young. The reproductive tracts and somatic organs of VAP1-immunized (n=7), control-immunized (n=3) and non-immunized (n=5) animals were collected and examined by histology and transmission electron microscopy. VAP1 immunization caused a strong and sustained immune response. Elevated levels of VAP1 antibody binding were detected in sera following initial injections, and immune titers rose as boosters were administered. Immunization had no adverse effect upon animal behavior or body condition. Immunized females demonstrated no major change in annual estrous cycling activity; however, the percentage of reproductive cycles resulting in pouch young decreased significantly (P<0.05) by 40%. Histological and ultrastructural analyses revealed an abundance of lipid-like degradation bodies within the ooplasm of developing oocytes and the cytoplasm of failing uterine zygotes. Active macrophage invasion of enlarged endometrial glands was observed in the uteri of two females. Reproductive tract changes are discussed in relation to observed fertility decline. The results of this study indicate that VAP1 has exciting potential as an immunocontraceptive target for possum control in New Zealand.


1973 ◽  
Vol 21 (3) ◽  
pp. 375 ◽  
Author(s):  
DJ Kitchener

The reproductive and associated organs of both male and female T. georgianus are briefly described. In females, only the right ovary is functional and pregnancies occur only in the right horn. They are monovular and the corpus luteum occupies most of the ovary and is deeply embedded in its stroma. Females are monotocous and the gestation period is probably about 4 months, young being born from October to February. They are monestrous and there is an autumn and early winter dioestrousanoestrous period. Spermatozoa are not stored in the reproductive tract of females and copulation appears to coincide with the oestrous condition. In males, spermatogenesis proceeds throughout the year and spermatozoa are present in the epididymis and vas deferens in all months that males were collected (no records for December). Spermatozoa are also found in the ampulla of Henle and vesicula seminalis in most months of the year. The position of the testes varies with season: in summer they descend to the scrota1 sacs; in autumn, winter, and spring they are more abdominal.


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.


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.


2006 ◽  
Vol 361 (1466) ◽  
pp. 269-275 ◽  
Author(s):  
M.T Siva-Jothy

The bed bugs and bat bugs (Hemiptera: Cimicidae) are unusual in being a gonochorist (separate male and female genders) taxon with obligate traumatic insemination. Males of all the species in this family have a lanceolate paramere (intromittent organ) which they use to pierce the female's body wall and inseminate directly into her haemocoel, despite the presence of a functional female genital tract. Mating is tightly linked to the feeding cycle in Cimex lectularius , the common bed bug. In this paper, I examine key aspects of the reproductive anatomy and behaviour of C. lectularius that underpin the nature of the conflict over mating rate in this species. I then examine the consequences of traumatic insemination for female fitness and examine potential mechanisms that might underpin those costs. Finally, the collateral consequences of the male reproductive tactic on other males of C. lectularius and the African bat bug, Afrocimex constrictus are examined.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Rama Singh ◽  
Santosh Jagadeeshan

The protein electrophoresis revolution, nearly fifty years ago, provided the first glimpse into the nature of molecular genetic variation within and between species and showed that the amount of genetic differences between newly arisen species was minimal. Twenty years later, 2D electrophoresis showed that, in contrast to general gene-enzyme variation, reproductive tract proteins were less polymorphic within species but highly diverged between species. The 2D results were interesting and revolutionary, but somewhat uninterpretable because, at the time, rapid evolution and selective sweeps were not yet part of the common vocabulary of evolutionary biologists. Since then, genomic studies of sex and reproduction-related (SRR) genes have grown rapidly into a large area of research in evolutionary biology and are shedding light on a number of phenomena. Here we review some of the major and current fields of research that have greatly contributed to our understanding of the evolutionary dynamics and importance of SRR genes and genetic systems in understanding reproductive biology and speciation.


2021 ◽  
Author(s):  
Oyovwi Mega Obukohwo ◽  
Nwangwa Eze Kingsley ◽  
Rotu Arientare Rume ◽  
Emojevwe Victor

The human reproductive system is made up of the primary and secondary organs, which helps to enhances reproduction. The male reproductive system is designed to produce male gametes and convey them to the female reproductive tract through the use of supportive fluids and testosterone synthesis. The paired testis (site of testosterone and sperm generation), scrotum (compartment for testis localisation), epididymis, vas deferens, seminal vesicles, prostate gland, bulbourethral gland, ejaculatory duct, urethra, and penis are the parts of the male reproductive system. The auxiliary organs aid in the maturation and transportation of sperm. Semen is made up of sperm and the secretions of the seminal vesicles, prostate, and bulbourethral glands (the ejaculate). Ejaculate is delivered to the female reproduc¬tive tract by the penis and urethra. The anatomy, embryology and functions of the male reproductive system are discussed in this chapter.


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