Functional morphology of the copulatory system of box crabs with long second gonopods (Calappidae,Eubrachyura, Decapoda,Crustacea)

Male True Crabs use two pairs of gonopods to deliver mating products during copulation. Commonly, the second pair is shorter than the first pair, and most research to date has focused on species with short second gonopods. We investigated male and female copulatory organs in Calappula saussurei and Calappa pelii, two species of box crabs (Calappidae) with second gonopods which are longer than the first pair. Scanning electron microscopy and histological cross sectioning show that the female copulatory system is unique in several aspects: the genital duct is part concave and part simple type. The seminal receptacle is divided into two chambers, a ventral chamber of ectodermal and mesodermal origin, and a dorsal chamber of ectodermal origin. This dorsal chamber is the location of spermatophore reception during copulation. A sperm plug closes the dorsal chamber off. We propose that long second gonopods deliver male mating products directly into the dorsal chamber. To date, spermatophore reception has been associated with the mesodermal tissue of the seminal receptacle. The copulatory system of box crabs with long second gonopods shows novel deviations from this general pattern. J. Morphol. 276:77–89, 2015. © 2014 Wiley Periodicals, Inc.     

Ultrastructure of the male reproductive system and spermatophore formation in Labidocera aestiva (Crust.: Copepoda)

Summary The male reproductive system of Labidocera aestiva produces a flask-shaped spermatophore connected to a chitin-like coupling apparatus. As immature spermatozoa leave the anterior region of the testis, they pass through the lumen of a long, sinuous duct composed of a ductus deferens and seminal vesicle. Ultrastructural examination of the ductus deferens reveals a highly glandular, columnar epithelium. The cells contain arrays of rough endoplasmic reticulum and abundant, well-developed Golgi complexes. This region produces and releases into the lumen, a flocculent substance and two granular secretions that constitute the seminal fluid. In its terminal part, the ductus deferens synthesizes another secretion that forms the spermatophore wall enclosing the spermatozoa and seminal fluid. Final synthesis of the spermatophore wall occurs within the thin-walled seminal vesicle, although this region functions primarily as a storage organ. Contiguous to the seminal vesicle is an elongate, highly glandular spermatophore sac. The chitin-like coupling apparatus, which functions to attach the spermatophore to the female, is formed in the anterior region of the sac by secretions from eight cell types. The posterior region of the sac stores the flask-shaped spermatophore and produces secretions that aid ejaculation of the entire spermatophore complex.Contribution No. 236, Harbor Branch Foundation, Inc.     

The role of cercal sensory feedback during spermatophore transfer in the cricket, Acheta domesticus

The role of the cerci in the spermatophore transfer behavior of the cricket Acheta domesticus was examined. During transfer, the male cerci were held close to the female abdomen where they produced small flicking movements. Male cercal ablation significantly decreased mating success by reducing both the ability of the male to hook the epiphallus on to the female subgenital plate and to transfer the spermatophore. During spermatophore transfer, the male must thread the spermatophore tube into the female genital papilla and attach the spermatophore, via its attachment plate, to the base of the ovipositor. Extracellular recordings from the male genital nerve revealed that a centrally driven, rhythmic bursting activity of genital efferents produced the rhythmic contractions of the five pairs of genital muscles responsible for spermatophore threading. Tactile stimulation of campaniform sensilla on the medial aspect of each cercus inhibited the activity of those motor units responsible for advancing the spermatophore tube during threading, while simultaneously activating the motor units responsible for adjusting the position of the epiphallus. We conclude that mechanosensory neurons on the cerci of the male cricket supply important information on female position to the motor program responsible for spermatophore threading and transfer.     

Spermatophore transfer in the hermit crab Clibanarius vittatus (Crustacea,Anomura, Diogenidae)

Although mating has been described in several hermit crab species, the mechanics of spermatophore transfer have not previously been demonstrated. Evidence from pleopod and gonopore morphology, video observations, and inseminated females indicates that in Clibanarius vittatus the male applies a spermatophoric mass directly onto the female via the gonopores rather than with modified pleopods 1-2 (gonopods) and/or genital papillae as in many other decapods. The single second pleopod of males of C. vittatus has a simple endopod with no apparent modifications for sperm transfer. There are no genital papillae extending from the male gonopores. The globular spermatophores are aligned in rows surrounded by a seminal secretion in the male ducts (vasa deferentia that terminate in ejaculatory ducts opening to the exterior via the gonopores). During copulation, described from time-lapse video recordings, the ventral surface of the last thoracic segment of the male, bearing the gonopores, was apposed to the ventral cephalothorax of the female. A massive amount of seminal secretion containing spermatophore ribbons, termed here the spermatophoric mass and described for the first time in a hermit crab species, was observed covering the sternites and coxae of pereopods 1-5 of a recently copulated female. It is suggested that during copulation the male emits the contents of the ejaculatory ducts directly onto the female without the aid of gonopods or genital papillae. Although spermatophore transfer is simple in C. vittatus, the presence of modified anterior pleopods or elongate genital papillae (sexual tubes) in other paguroidean species suggests the possibility of a more complex insemination process in these other hermit crabs.     

Spermatophore formation in the pseudoscorpion Chthonius ischnocheles (Chthoniidae)

The reproduction of pseudoscorpions involves indirect sperm transfer by means of spermatophores. The spermatophores are the product of the male genital atrium. A functional interpretation of spermatophore formation in Chthonius ischnocheles is based on evidence from (a) a morphological study of the genital atrium, the associated accessory glands and the musculature (b) males sectioned during spermatophore production (c) histochemical tests on the glands and their secretions (d) biochemical analyses of one gland (posterior dorsal) and its secretion (e) the behaviour of males during this process and (f) the structure of the spermatophore.
The anterior region of the genital atrium is concerned with the production of the sperm packet. The encysted sperm and the seminal fluid from the prostatic reservoir are encapsulated in a sperm packet by a secretion from two pairs of anterior glands. The posterior region of the genital atrium is responsible for the formation of the spermatophore stalk and its distal elaboration, the two lateral collars. These parts of the spermatophore arise from the fibroin secretion of the posterior dorsal gland; the shape of the spermatophore collars is correlated with their mould, the medial diverticula. In addition the lateral glands secrete a light oil which accumulates on a thickening of the spermatophore stalk proximal to the collars. This suggested that this secretion acts as a pheromone to attract females to the spermatophore since in this species males produce their spermatophores in the absence of females.     

External Anatomy of the Female Genital (Eighth) Limbs and the Setose Openings in Myodocopid Ostracodes (Cypridinidae)

The external anatomy of various cypridinid female genital (8th) limbs is described. Scanning electron microscopy shows that each female cypridinid genital limb has a medial depression and associated pore (= spermatophore pore); over all of which a male cements a spermatophore. The limb terminates laterally in a superficially smooth rounded knob bearing an additional small opening (= lateral pore). Dorsolateral to this genital limb there are grouped setae, previously called "brush organs", that are really paired, slit–like posterolateral openings, which are probably subdermally united to the female genital limbs. The "brush organs" of all myodocopid females also are likely to be the setose openings. The setose openings are probably homologous to the setose central lobe of male cypridinid copulatory limbs, but not homologous to the limb–like "brush organ" described for some podocopid males. We speculate that the eggs are fertilized via the spermatophore pore associated with the attached spermatophore, and that they are released from the slightly larger and more lateral setose openings into the brood chamber of the posterodorsal area of the bivalved carapace.     

Correlation Between the Mesodermal Male Genital Ducts and the Spermatophore Structure in a Ditrysian Moth,Zygaena trifolii (Esper, 1783) (Insecta,Lepidoptera, Zygaenidae)

Abstract The mesodermal male genital system and the spermatophore of Zygaena trifolii (Insecta, Lepidoptera, Zygaenidae) have been studied histologically. Whereas the long unpaired duct, the ductus mesospermaticus, has been found to consist of at least six distinctly different regions, the tissues and secretions of the seminal vesicles and the accessory glands were found to be quite uniform. Several of the different regions are separated from each other by epithelial septa (constrictions). The external structure and the internal organization of the spermatophore are described. Based on histological comparisons, the correlation between the contents of the spermatophore and the different parts of the male system is given.     

Mode of transfer of spermatozoa in Orthoptera Tettigoniidae

A morphological and ultrastructural study was carried out on the spermatophore and spermatodoses of some species of Orthoptera Tettigoniidae. From the results concerning the spermatophore it emerged that this structure has a morphological and ultrastructural organization represented by a dilated ampulla and a peduncle or neck. From the examination of freshly deposited spermatophores and those at various time intervals thereafter, it was seen that these structures other than allowing gamete transfer, represent the site where spermatodesms, organized in the male genital tracts, undergo reorganization to acquire their definitive morphological and structural characteristics as found in the female genital tracts. The spermatodoses, in the same way as the spermatophore, represent capsules containing spermatodesms, which are originated in the spermatheca, their specific morphology seems to diversify according to the species considered. As regards their role, it is hypothesized that these structures represent a long-term conservation mechanism for spermatozoa inside the seminal receptacle.     

Courtship and sperm transfer in Charinus neocaledonicus Kraepelin, 1895 and Charinus australianus (L. Koch, 1867) (Arachnida, Amblypygi, Charinidae)

The Charinus australianus group is a well-defined species group characterised by rounded, cushion-like female gonopods. Before the present study, the morphology of the gonopods and their function have not been understood. This paper describes courtship behaviour, spermatophore morphology, and the morphology of the female genitalia of Charinus neocaledonicus Kraepelin, 1895 and C. australianus (L. Koch, 1867). Courtship behaviour, though different in details, is similar to that of many other species. The spermatophores are large and soft and carry very small sperm packages, each with a short stalk. After sperm transfer, the spermatophore may be eaten by the female. The spermatophore thus transfers not only spermatozoa but also nutritious paternal investment to the female. Each female gonopod is equipped with a seminal receptacle consisting of an atrium and a spacious inner receptacle. The cover of the atrium can be elevated by high blood pressure and pulled back by a group of muscles attached to the inner part of the receptacle. The female probably picks up the sperm packages with the atria of her receptacles. The observations are compared to those on other amblypygids, and the evolution of different types of spermatophores and of gonopods with seminal receptacles is discussed.     

Mating and the inferred function of the genital system of the nudibranch, Aeolidiella glauca (Gastropoda: Opisthobranchia: Aeolidioidea)

Abstract. We describe the genital system of the aeolid nudibranch gastropod Aeolidiella glauca as a basis for our ongoing analysis of the mating system of this hermaphroditic species. In addition we give a short account of its mating behavior. A. glauca has an androdiaulic genital system with a proximally situated semiserial seminal receptacle. There is no bursa copulatrix. After fertilization, eggs pass through six glands, i.e., the capsule gland and the female gland mass which is comprised of five histologically differentiated parts. The prostate is a long, glandular tube. The everted, unarmed penis is very large and bears a series of 3–4 hook-shaped lobes consisting only of a simple, ciliated epithelium on its ventral side. Their function is unknown. After courtship, which involves moving in circles followed by resting in a head-to-head position, reciprocally touching each other with the tentacles, the slugs glide into a position where the everted genital atria are in contact. The huge penes are protruded simultaneously shortly after this contact occurs. Each animal strokes its partner's back with the penis and deposits a spermatophore of undetermined shape onto the partner's notum. Sperm enter the recipient through histolysis. How the sperm find their way to the seminal receptacle is not known.     

Studies on in vitro Extrusion and Ultrastructure of the Spermatophore in Haemaphysalis longicornis (Acari: Ixodidae)

Copulation in ticks is completed by the insertion of the spermatophore into the female genital aperture by a male. The endospermatophore, a cord-like structure and contents are packed in the ectospermatophore of the completed spermatophore. The endospermatophore extrudes just after insertion of the tip of the spermatophore. Only the endospermatophore enters the female genital tract, and the ectospermatophore remains outside the female body. The extrusion is observed in vitro in Haemaphysalis longicornis at various concentrations of NaCl solution: the process is accelerated in less concentrated solutions. The cord-like structure and the endospermatophore finally receive contents extruded from the ectospermatophore. The tip of the cord-like structure connects to the surface of the endospermatophore, and together form a loop after extrusion. Ultrastructural observations confirmed that the ectospermatophore wall is composed of four layers, and the contents consist of male germ cells and three types of secretions from the male accessory genital glands. As in other ticks the male germ cells are elongated spermatids in spermatophores just after formation and extrusion. Adlerocysts described in other ticks are not found in the spermatophore of H. longicornis.     

Sinohesione genitaliphora gen. et sp. n. (Polychaeta, Hesionidae), an interstitial annelid with unique dimorphous external genital organs

A new hesionid. Sinohesione genitaliphora gen. et sp. n., is described from intertidal sandy sediments of Hainan Island, China. It differs from hitherto known hesionids by the presence of external genital organs in both sexes. In the males there is one pair of sae-like appendages, each bearing a tube-shaped penis, on chaetiger 10. In the females the paired sae-shaped organs are situated on chaetiger 12. Reconstructions of semi- and ultrathin sections show that a long, heavily coiled sperm duct opens at the tip of each penis. The duct opens with a ciliated funnel into a seminal vesicle in chaetiger 9. Prominent gland cells surround the sperm duct for the most part. The female genital organs each have two openings; one of which leads to a blind ending seminal receptacle. The other is the external pore of a ciliated oviduct that originates as an open funnel in the coelom of chaetiger 10. The functional and phylogenetic significance of these structures is discussed.     

The functional significance of the spermatophore and the fate of spermatozoa in the genital tract of Helix pomatia (Gastropoda: Stylommatophora)

In the Helicidae and in some other Stylommatophora the sperm are transferred in a spermatophore, even though there appears to be no need for protection of the sperm during the transfer. The function of the spermatophore and related problems concerning the genital organs of Helix pomatia were studied by means of morphological and experimental methods.
The spermatophore is necessary to ensure the functioning of the female system at copulation. Its structure allows some of the spermatozoa it contains to escape through its tail canal, pass from the stalk of the bursa and reach the spermatheca by way of the oviduct; but most of the sperm pass into the bursa copulatrix and are destroyed, as is also the fate of the spermatophore. Only foreign sperm are stored in the spermatheca.
Spermiogenesis was found to take place throughout the whole summer. At intervals some sperm are released from the hermaphrodite duct and are conducted via the spermoviduct and oviduct to the bursa, where they are digested. The two grooves of the spermoviduct are functionally separated only for a few minutes at actual copulation, when sperm are conducted to the copulatory organs, where the spermatophore is being formed.     

Spermatodesm reorganization in the spermatophore and in the spermatheca of the bushcricket Tylopsis liliifolia (Fabricius) (Orthoptera,Tettigoniidae)

Spermatozoa of Tettigoniidae are usually transferred to the female by means of a spermatophore which is also the site of feather-shaped spermatodesm formation. These spermatodesms are then transferred to a spermatheca, composed of a spermathecal duct and of a seminal receptacle, involved in storing spermatozoa. In order to extend the knowledge about sperm transfer and spermatodesms reorganization in the Tettigoniidae, a morpho-structural investigation was carried out on spermatophore and spermatheca of Tylopsis liliifolia and on the reorganization of the gametes from the spermatophore. Our results show that the spermatodesms undergo disorganization in the spermatophore; unlike other Tettigoniidae, however, feather-shaped spermatodesms are never found. The epithelium of the spermatheca consists of two cell types, the cuticle-forming and the gland cells, with secretory features. The gland cells, absent in the distal tract of the seminal receptacle, release their secretion in a “reservoir” where an efferent duct opens. In the distal tract of the spermathecal duct, adjacent epithelial cells show diversified ultrastructural characteristics whose probable role is discussed. A particular feature of T. liliifolia is the genesis of the feather-shaped spermatodesms in the seminal receptacle. This feature and the peculiar organization of the feather-shaped spermatodesm are a possible autapomorphy of T. liliifolia.     

Copulation, genital damage and early death in Callosobruchus maculatus

Antagonistic sexual coevolution stems from the notion that male and female interests over reproduction are in conflict. Such conflicts appear to be particularly obvious when male genital armature inflicts damage to the female reproductive tract resulting in reduced female longevity. However, studies of mating frequency, genital damage and female longevity are difficult to interpret because females not only sustain more genital damage, but also receive more seminal fluid when they engage in multiple copulations. Here, we attempt to disentangle the effects of genital damage and seminal fluid transfer on female longevity in the beetle Callosobruchus maculatus (Coleoptera: Bruchidae). Males copulating for the sixth time in succession inflicted greater levels of genital damage, but transferred smaller ejaculates in comparison with virgin males. The number of copulations performed by males was negatively related to female fecundity and positively related to female longevity, suggesting a trade-off between fecundity and longevity. However, inclusion of fecundity as a covariate revealed sperm and/or seminal fluid transfer to have a negative impact on female longevity above that caused by the fecundity-longevity trade-off. The consequences of multiple copulations on female longevity were examined. Females that mated twice laid more eggs and died sooner than those that mated once. However, incorporation of fecundity as a covariate into our statistical model removed the effect of female mating frequency on female longevity, indicating that double-mated females suffer greater mortality owing to the trade-off between fecundity and longevity. Males of this species are known to transfer very large ejaculates (up to 8% of their body weight), which may represent a significant nutritional benefit to females. However, the receipt of large ejaculates appears to carry costs. Thus, the interpretation of multiple mating experiments on female longevity and associated functional explanations of polyandry in this species are likely to be complex.     

The evolution of a female genital trait widely distributed in the Lepidoptera: comparative evidence for an effect of sexual coevolution

Background

Sexual coevolution is considered responsible for the evolution of many male genital traits, but its effect on female genital morphology is poorly understood. In many lepidopterans, females become temporarily unreceptive after mating and the length of this refractory period is inversely related to the amount of spermatophore remaining in their genital tracts. Sperm competition can select for males that delay female remating by transferring spermatophores with thick spermatophore envelopes that take more time to be broken. These envelopes could select for signa, sclerotized sharp structures located within the female genital tract, that are used for breaking spermatophores. Thus, this hypothesis predicts that thick spermatophore envelopes and signa evolve in polyandrous species, and that these adaptations are lost when monandry evolves subsequently. Here we test the expected associations between female mating pattern and presence/absence of signa, and review the scant information available on the thickness of spermatophore envelopes.

Methodology/Principal Findings

We made a literature review and found information on female mating pattern (monandry/polyandry), presence/absence of signa and phylogenetic position for 37 taxa. We built a phylogenetic supertree for these taxa, mapped both traits on it, and tested for the predicted association by using Pagel''s test for correlated evolution. We found that, as predicted by our hypothesis, monandry evolved eight times and in five of them signa were lost; preliminary evidence suggests that at least in two of the three exceptions males imposed monandry on females by means of specially thick spermatophore envelopes. Previously published data on six genera of Papilionidae is in agreement with the predicted associations between mating pattern and the characteristics of spermatophore envelopes and signa.

Conclusions/Significance

Our results support the hypothesis that signa are a product of sexually antagonistic coevolution with spermatophore envelopes.     

Reproduction in the genus Limacina (Opisthobranchia: Thecosomata)

Reproductive mechanisms in the seven species of the thecosomatous pteropod genus Limacina are described and compared. All species are protandrous hermaphrodites. Five species– L. bulimoides, L. helicina, L. lesueuri, L. retroversa and L. trochiformis –have a similar reproductive anatomy in which the gonoduct leading from the gonad to the common genital pore functions as a seminal vesicle in the male and is elaborated into mucous and albumen glands in the female. The male system consists of a prostate gland and penis connected to the common genital pore by an external ciliary tract. All five species have a free-swimming veliger stage which hatches from free-floating egg masses. Limacina helicoides has the same reproductive anatomy but is ovoviviparous, with embryos retained in capsules in the mucous gland until they are juveniles of 50 mm in shell diameter. Limacina inflata lacks mucous and albumen glands and a penis; a spermatophore formed by the prostate gland is used in aphallic sperm transfer. This species exhibits brood protection with un-encapsulated embryos retained in the mantle cavity until they are released as veligers measuring 0067 mm in diameter. L. inflata is the most abundant of the seven species despite lowered fecundity; reasons for its ecological success are discussed.     

Morphological association between spermatophores and male genitalia in carabid beetles of the tribe Pterostichini (Coleoptera: Carabidae)

A morphological association between genitalia and ejaculates could provide insight into the function and evolution of genitalia. In this study, the morphologies of the ejaculates and male genitalia of 15 species of Pterostichini and two species of Platynini (Coleoptera: Carabidae) are described. All the species examined formed a spermatophore, the morphology of which could be classified into three types based on its relative volume in the female vaginal cavity and the presence or absence of a pluglike conformation. Male genital morphology could be divided into two types by the direction of the endophallus and gonopore. Species with a strongly bent endophallus invariably formed a pluglike spermatophore. The results suggest that the peculiar shape of endophallus found in some species of Pterostichini may function in forming the pluglike structure of the spermatophore.