Memoirs: On the Development of the Male Genitalia and the Efferent Genital Ducts in Lepidoptera

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.

1958 ◽  
Vol 36 (5) ◽  
pp. 753-777 ◽  
Author(s):  
Russell Y. Zachakuk

In the male larva of Ctenicera aeripennis destructor (Brown), the reproductive system consists of paired mesodermal gonads situated in one of the second to fifth segments of the abdomen, an ectodermal genital capsule and paired mesodermal ampullae situated in the ninth segment of the abdomen, and a pair of mesodermal cell strands that connect the gonads to the ampullae. In the female larva, the reproductive system consists of paired mesodermal gonads situated similarly to those of the male, paired mesodermal ampullae situated at the posterior margin of the seventh segment, and a pair of mesodermal cell strands that connect the gonads to the ampullae. During the larval stage, prepupal period, and pupal stage, the gonads and cell strands of the male develop into testes and vasa deferentia, respectively, and those of the female, into ovaries and lateral oviducts, respectively. In the male, during the prepupal period and pupal stage, the ampullae develop into the paired spermatophoral and accessory glands and the seminal vesicles; the genital capsule develops into the ejaculatory duct and external genitalia. In the female, during the prepupal period and pupal stage, the ampullae develop into the common oviduct; the vagina forms from a groove in the ventral epidermis of the eighth and ninth abdominal segments; the uterus, spermatophoral receptacle, spermatheca, accessory gland, and its duct develop from invaginations in the vaginal groove in the eighth abdominal segment; the external genitalia develop from ridges on the sternal epidermis of the ninth abdominal segment.


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.


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.


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.


1924 ◽  
Vol s2-69 (273) ◽  
pp. 59-96
Author(s):  
HEM SINGH-PRUTHI

(a) Internal Genital Ducts. In young Homoptera nymphs the male efferent genital system consists of a pair of vasa deferentia, which are anteriorly continuous with the testes, and a pair of terminal ducts of hypodermal origin which are at this stage not connected with the vasa deferentia. The terminal unpaired common ejaculatory duct arises later as a solid ingrowth of the integument; anteriorly it meets the blind ends of the paired hypodermal ducts. It soon acquires a lumen and freely communicates with the exterior. At a slightly later stage of development the paired hypodermal ducts, by a constriction in the horizontal plane along the whole of their length, become two pairs, a dorsal and a ventral, the accessory glands and the paired ejaculatory ducts respectively. The paired ejaculatory ducts communicate with the vasa deferentia at a much later stage of development. The vesiculae seminales develop from the distal ends of the vasa deferentia. The above mode of development lends great support to the view (Palmen) that primitive insects had a pair of terminal ducts, and clearly indicates that these ducts were ectodermal and not mesodermal as stated by Palmen. As shown by Nüssbaum in some other insects, of the efferent systems all organs except the vasa deferentia are of an ectodermal origin. But the way in which the common ejaculatory duct, the accessory glands, and the vesiculae seminales arise in Homoptera is quite different from that suggested by Nüssbaum. Unpaired organs are unpaired from the very beginning, they do not arise by the coalescing of paired organs, as this author believed. (b) External Genital Appendages. The male genitalia of the adult Homoptera consist of two pairs of lateral appendages, the sub-genital plates and the parameres, and a median copulatory organ, the aedeagus. They are all borne by the ninth abdominal segment. They develop from two pairs of appendages only, an outer and an inner, which appear as diverticula of the ventral region of the ninth segment. The outer pair develops into the subgenital plates, and the inner by longitudinal fission becomes two pairs; the inner one of the two pairs so obtained, by the fusion along the median line of its components, forms a single organ, the aedeagus. while the outer is transformed into the parameres. Thus the pair of appendages developing into the sub-genital plates does not belong to the eighth segment, as was believed by Kershaw and Muir, but to the ninth ; there are no appendages on the eighth in the nymphs or in the adult; nor is there any evidence in favour of these authors' view that the male gonopore in Homoptera, unlike that in most orders of insects, lies between the eighth and ninth sterna ; it is in its usual place, behind the ninth sternum. The sub-genital plates seem to be the coxites of the ninth sternum; and both the aedeagus and the parameres, derived from a primitively single pair of appendages, correspond to the endopodites. As in Homoptera, in insects in general there are, besides the median aedeagus, two pairs of appendages in connexion with the ninth (the coxites and parameres). and not one as hitherto believed. But generally one pair is developed, e. g. coxites in Ephemeroptera, Lepidoptera, Diptera, &c. ; parameres in Heteroptera, Orthoptera, Coleoptera, &c. Only rarely both pairs are present, e.g. Hymenoptera, Homoptera, Thysanura, some Diptera. The fact that usually only one pair occurs seems to be responsible for the notion that the male genitalia of insects consis of, tbesides the aedeagus, only one pair of appendages. This also explains why this one pair of appendages could not be homologized in the different orders. In male Homoptera, as in most other insects, the homologues of the anterior pair of ovipositor-lobes, believed by Kershaw and Muir to be represented by the sub-genital plates, are not present; the sub-genital plates correspond to the lateral ovipositor-lobes ; and the dorsal pair of ovipositor-lobes ia represented by both the aedeagus and the parameres, and not by aedeagus or parameres alone as hitherto believed.


BMC Zoology ◽  
2022 ◽  
Vol 7 (1) ◽  
Author(s):  
Josefine Kreuz ◽  
Monika J. B. Eberhard

Abstract Background Asymmetries are a widespread phenomenon in otherwise bilaterally symmetric organisms, and investigation of asymmetric structures can help us gather insights into fundamental evolutionary processes such as the selection for morphological novelties caused by behavioural changes. In insects, asymmetric genitalia have evolved in almost every order, and usually it’s the sclerotized parts and most conspicuous male phallic organs that are known to exhibit asymmetries. While external copulatory organs in insects have often been subject to investigations concerning asymmetries and the evolution thereof, internal reproductive structures have received far less attention. Here we describe the internal and external male genitalia in three species of Austrophasmatidae, Mantophasmatodea, using μ-CT imaging and light microscopy. Mantophasmatodea is the most recently discovered insect order, and with 21 species described to date, it is among the smallest insect orders currently known. Results We confirm that male heelwalkers exhibit asymmetries in the external genitalia and associated structures, represented by asymmetric phallic lobes and cerci. Moreover, we found an extreme asymmetry within the internal male genitalia: in all adult males investigated (N = 5), the seminal vesicle, a dilatation of the vas deferens, was only developed on the right side of the male while missing on the left side. Conclusion The false-male-above mating position exhibited by Mantophasmatodea and especially the long copulation duration of ca. 3 days might select for this unusual absence asymmetry of the left seminal vesicle. If this holds true for all heelwalker species, this absence asymmetry constitutes another autapomorphy for Austrophasmatidae or even the insect order Mantophasmatodea.


2020 ◽  
Vol 20 (4) ◽  
Author(s):  
Vinícius Albano Araújo ◽  
Tito Bacca ◽  
Lucimar Gomes Dias

Abstract: Pentatomidae comprises a diverse group of stink bugs widely distributed in the Neotropical region. Many species are phytophagous and cause injuries to plants, and can thus be defined as agricultural pests. In this study, the anatomy of the female and male reproductive tracts of three important agricultural pests in Colombia is described: Piezodorus guildinii Westwood, 1837 and Chinavia ubicaRolston 1983, found on soybeans, and Oebalus insularis Stål, 1872, found in rice crops. For that, light microscopy techniques were used. The anatomy of the reproductive tract of sexually mature males of the three species studied consisted of a pair of testes, vas deferens, seminal vesicles, ejaculatory bulb, an ejaculatory duct that opens into an aedeagus, and paired accessory glands. The reproductive tract of females consisted of a pair of ovaries, each with seven telotrophic-meroistic ovarioles, a pair of lateral oviducts, common oviduct, spermatheca, and a genital chamber. Telotrophic ovarioles were comprised of terminal filament, tropharium, vitellarium, and pedicel. Differences in size, color, and position of structures along the reproductive tract were observed between the species examined. Reproductive biology of insects provides informative characters for behavioral and evolutionary studies, as well as useful data for pest control strategies.


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.


2018 ◽  
Vol 58 (1) ◽  
pp. 91-125 ◽  
Author(s):  
Valentina Castro-Huertas ◽  
Dimitri Forero ◽  
Jocelia Grazia

The assassin bug tribe Metapterini belongs to the subfamily Emesinae (Hemiptera: Heteroptera: Reduviidae). Morphologically, it is characterized by the conspicuous basal process of the posteroventral series in the foreleg and the presence of wing polymorphism, with a high proportion of the genera with micropterous or apterous species. Here, the male and female ectodermal genitalic structures are documented for ten genera and twenty-three species of Metapterini, including eight species of the speciose genus Ghilianella Spinola, 1850. Descriptions and digital macrophotographs are provided for abdominal segment 8, pygophore, parameres, and phallus of the male, and for tergite 8, tergite 9, gonocoxae, gonapophyses, gonoplac, and bursa copulatrix of the female. The asymmetric male genitalia within Emesinae are discussed. From this morphological documentation sixty six phylogenetic characters are coded, presented as a data matrix and analyzed cladistically, and their potential usefulness for resolving relationships among Metapterini is discussed.


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