Memoirs: The Development of the Male Genitalia of Homoptera, with Preliminary Remarks on the Nature of these Organs in other Insects

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.

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.


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.


Zootaxa ◽  
2006 ◽  
Vol 1164 (1) ◽  
pp. 35
Author(s):  
PASI SIHVONEN ◽  
DIETER STÜNING

The Palaearctic Scopula dubernardi species group (Lepidoptera: Geometridae) is revised on the basis of external and genitalic characters to include Scopula dubernardi (Oberthür, 1923) and Scopula segregata Prout, 1919. Lectotypes are designated for both species, which were described from more than one specimen without holotype designation. The species delimitation is based on small quantitative differences in the female genitalia, i.e., the degree of turn of the ductus bursae along its axis, and on external features. Furthermore, the recognition of the studied taxa as separate species is strengthened by the observation that they occur sympatrically and synchronously in two localities. Unlike the common situation in the genus Scopula, structures of the male genitalia were found uninformative in species delimitation. The length of right ceras on the 8th sternite of S. segregata was found to be polymorphic. Adults and genitalia of S. dubernardi and S. segregata are illustrated, along with the variation in external features and genitalia in both species. The biology and immature stages of both species are unknown.


2018 ◽  
Vol 193 ◽  
pp. 04003
Author(s):  
Thanh Son Le

Ecological Architecture is a modern topic. In Viet Nam, this topic attracted a great attention, and eventually, it is considered as a new trend, both theoretical and practical. This article presents different perspectives, but not the common public opinions on the issue, in particular, as follows: comparison of the relationship between the traditional Vietnamese architecture and the modern ecological architecture to acknowledge the similarity rather than the difference; the lessons learned from a particular stage of development in Vietnam before 1975 as an empirical result for modern ecological and environmental theories; discussion of the missed opportunity for the integration and contribution of modern Vietnamese architecture in terms of both theoretical and ecological development of Vietnamese architecture in the context of globalization.


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.


1961 ◽  
Vol 93 (11) ◽  
pp. 1044-1047 ◽  
Author(s):  
G. E. Shewell

Distinguished from the common ‘cluster fly’, Pollenia rudis (Fab.) as follows: Mesonotum with a median stripe anterior to transverse suture (readily seen with naked eye in oblique posterior view). Basicosta black (in rudis it is reddish-brown in female but inclined to be darker in male especially towards the base). Tessellation of abdomen less broken, the contrasting pollinose areas larger and more regular (rectangular) in outline. Abdominal pollen cinereous with bluish reflection (dull yellowish in rudis). Male genitalia (Figs. 1-3) with forceps and aedeagus longer and more slender.


1996 ◽  
Vol 89 (1) ◽  
pp. 19-40 ◽  
Author(s):  
Michael L. Satlow

What does it mean “to be a man”? Whereas in most societies at most times the determination of “maleness” is straightforward (does he have male genitalia? what is his chromosomal make-up?), locating the cultural constructions of “manhood” is far more difficult. Many anthropologists have noted that in contrast to models that postulate a common psychology for all men, everywhere, all the time, constructions of manhood are varied and culturally dependent. For example, the highly aggressive behavior necessary for retention of manhood for a male resident of Andalusian Spain can be contrasted to the sanctioned behavior of males of Tahiti. Unifying these diverse constructions of masculinity, however, is the common idea that manhood is an acquired state that males must fight both to attain and maintain. Because manhood is an achieved state, it can never be taken for granted: a male must be constantly proving that he is a man. “[T]he state of being a ‘real man’ or ‘true man’ [is] uncertain or precarious, a prize to be won or wrested through struggle.” Similar constructions of manhood are evident today throughout the circum-Mediterranean.


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.


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