Description of the male reproductive system of Paguristes eremita (Anomura, Diogenidae) and its placement in a phylogeny of diogenid species based on spermatozoal and spermatophore ultrastructure

The male gonopores, male reproductive apparatus, spermatophore and spermatozoa of the Mediterranean hermit crab Paguristes eremita are described, using interference phase microscopy, scanning electron microscopy and transmission electron microscopy. A correlation is made between the gonopore morphology and the different kinds of setae accompanying them, and the reproductive biology of these crabs. Each testes merges into a tubular duct made up of four zones: (1) the collecting tubule with free spermatozoa; (2) the proximal zone, where the ampulla of the spermatophores starts to be formed; (3) the medial zone, where the ampulla is completed, the stalk lengthens and the pedestal is formed; (4) the distal zone, where the mature spermatophores are stored. The sizes of the different parts of the spermatophore and of the sperm are given and their exterior morphology and ultrastructure described and compared to congeners. The morphology of the gonopore, male reproductive system, spermatophore and spermatozoa of P. eremita are species-specific, clearly distinguishing the species from the other members of the family. The available spermatozoal and spermatophore data is used to place P. eremita within a sperm phylogeny of the hermit crab family Diogenidae.     

Last–male sperm precedence in the bushcricket Poecilimon veluchianus (Orthoptera, Tettigonioidea) demonstrated by DNA fingerprinting

Males of the bushcricket Poecilimon veluchianus pass a large spermatophore to the female during mating. The spermatophore is eaten by the female after copulation. Because females mate with several males during their reproductive life, the competition between spermatozoa of different males affects a male's reproductive success. In order to determine the outcome of sperm competition, the paternity of the progeny of double–mated females was established by DNA fingerprinting with the oligonucleotide (GATA)₄. Typical P. veluchianus DNA fingerprints consisted of 15 scoreable fragments per individual. The proportion of bands shared between presumably unrelated bushcrickets was 17%. After the second copulation the second mating male clearly predominated at fertilization. The mean proportion of eggs fertilized by the second male was 90.1%. There was no significant relationship between the level of sperm precedence and the time of ovipositions after the second mating. If female P. veluchianus increase the fitness of their offspring by the incorporation of spermatophore–derived substances in developing eggs, there is little chance for the feeding male to fertilize eggs containing his nutrients, because of the very short mating intervals of females and the observed high level of last–male sperm precedence in this species. Under such conditions the last mating male would fertilize many eggs containing nutrients from a prior male. Because nuptial gifts, like the tettigoniid spermatophore, function only as paternal investment if the donating male's progeny benefit from the gift, a paternal investment function of the P. veluchianus spermatophore seems to be unlikely.     

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.     

Morphology of the male reproductive system and spermatophore formation in the freshwater 'red claw' crayfish Cherax quadricarinatus (Von Martens, 1898) (Decapoda, Parastacidae)

The morphology of the male reproductive system was studied in Cherax quadricarinatus. The testes and vasa deferentia were dissected, fixed, cut and stained. Testes appear as two parallel and opalescent strands; they present many testicular lobes, each lobe containing cells in the same stage of the spermatogenic cycle. A vas deferens arises from the external side of each testis and three parts were clearly distinguished: proximal vas deferens (PVD), middle vas deferens (MVD) and distal vas deferens (DVD). The PVD is opalescent and highly convoluted, the MVD is pale white in colour and convoluted, but wider in diameter than the PVD, while the DVD shows the widest diameter, is straight and is white in colour. A single‐layered epithelium is recognized in the vas deferens; with cylindrical cells in the PVD and cuboid cells in the MVD and DVD. The formation of the spermatophore starts at the PVD, while the secondary layer of the spermatophore seems to be added at the MVD. At the DVD, the highly coiled spermatophore is surrounded by the periodic acid Schiff‐positive sticky components of the secondary layer. Many aspects of spermatophore formation in C. quadricarinatus differ from those of other Astacida. The applied aspects of this study for aquaculture purposes are discussed.     

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.     

Male Aggression,Female Mimicry and Female Choice in the Rove Beetle,Aleochara curtula (Coleoptera,Staphylinidae)

Causes, consequences and pheromonal regulation of male contest and female choice in the staphylinid beetle, Aleochara curtula (Goeze), have been investigated in the field and in the laboratory. At the feeding and mating site (carcass) the sex ratio is male biased. Polyandry is affected by prolonged copulations, spermatophore plugs and anti-aphrodisiac pheromones transferred from the male, and by female repulse behaviour as well. Aggression of competing males leads to expulsion of inferior males from the carcass. Young, starved and multiply mated males, which need access to the food resource, produce the female sex pheromone. They release homosexual responses, but also avoid intrasexual aggression. On the other hand, females behave aggressively towards individuals bearing the female sex pheromone or repulse their copulatory attempts. Those males of insufficient physiological condition produce a lighter spermatophore and fertilize less eggs. The adaptive significance of female mimicry, male mating tactics, and female choice is discussed.     

Internal anatomy and ultrastructure of the male reproductive system of the spider crab Maja brachydactyla (Decapoda: Brachyura)

The morphology and function of the male reproductive system in the spider crab Maja brachydactyla, an important commercial species, is described using light and electron microscopy. The reproductive system follows the pattern found among brachyuran with several peculiarities. The testis, known as tubular testis, consists of a single, highly coiled seminiferous tubule divided all along by an inner epithelium into germinal, transformation, and evacuation zones, each playing a different role during spermatogenesis. The vas deferens (VD) presents diverticula increasing in number and size towards the median VD, where spermatophores are stored. The inner monostratified epithelium exocytoses the materials involved in the spermatophore wall formation (named substance I and II) and spermatophore storage in the anterior and median VD, respectively. A large accessory gland is attached to the posterior VD, and its secretions are released as granules in apocrine secretion, and stored in the lumen of the diverticula as seminal fluids. A striated musculature may contribute to the formation and movement of spermatophores and seminal fluids along the VD. The ejaculatory duct (ED) shows a multilayered musculature and a nonsecretory pseudostratified epithelium, and extrudes the reproductive products towards the gonopores. A tissue attached to the ED is identified as the androgenic gland.     

Chonopeltis australis (Crustacea) male reproductive system morphology; Sperm transfer and review of reproduction in Branchiura

The morphology of the male reproductive system as well as sperm transfer in Branchiura has been described for Dolops ranarum and Argulus japonicus. In this study, the reproductive system and accessory structures are described for male Chonopeltis australis using histology, light microscopy, and scanning electron microscopy. For the first time, we describe sperm transfer by means of a spermatophore in this genus. The internal and external morphology and mechanism of sperm transfer is compared with other Branchiura, where it has been described. The morphology of the reproductive system of C. australis is similar to that of D. ranarum while the accessory structures and the spermatophore produced are similar to that of A. japonicus. A revision of the definition of Branchiura with respect to reproduction is provided. J. Morphol. 276:209–218, 2015. © 2014 Wiley Periodicals, Inc.     

The function of mate guarding in a field cricket (Orthoptera: Gryllidae;Teleogryllus natalensis otte and cade)

Three hypotheses relating to the function of postcopulatory mate guarding were tested for the cricketTeleogryllus natalensis. The hypothesis that guarding allows the male to remain with the female for repeated matings was rejected. This was because the mean intercopulatory interval for maleT. natalensis was found to be nearly twice as long as the mean duration of guarding. Nor do the results provide evidence to support the hypothesis that guarding functions to prevent copulation attempts by rival males (the rival exclusion hypothesis): the presence of a rival male was found to have no significant effect on the duration of spermatophore attachment for either guarded or unguarded females. The results do, however, support a third hypothesis, namely, that guarding functions to prevent the female from removing the spermatophore ampulla before complete sperm transfer. As predicted by this hypothesis, the presence of a guarding male was found to have a significant positive effect on the duration of spermatophore attachment. Further support for this hypothesis was provided by the fact that there was a significant positive correlation between the duration of mate guarding and the duration of spermatophore attachment.     

Male reproductive system in Neorossia caroli (Joubin 1902) (Cephalopoda: Sepiolidae) from Sardinian waters (western Mediterranean Sea) with particular reference to sexual products

The male reproductive system of the bobtail squid Neorossia caroli (Cephalopoda: Sepiolidae) is described in detail, based on observations of 90 mature males caught from 500 to 1600?m depth in Sardinian waters (western Mediterranean Sea). Reproductive organs in mature specimens accounted for up to 6% of total body weight. Of this, 70% was represented by the spermatophoric complex. Up to 83 spermatophores were found inside the Needham's sac. Mean spermatophore length was 16.7?mm. Sperm mass, cement body, and ejaculatory apparatus represented 63.2%, 13.1%, and 23.7% of the total spermatophore length, respectively. Inverted spermatophores, empty spermatophore sheaths, and spermatangia were also found in the sac, and their presence is discussed. Spermatangia implanted in several parts of the bodies of males (e.g., head, funnel, and eyes) were recorded and their occurrence is discussed. The spermatophoric reaction was induced in the laboratory by submerging spermatophores in seawater, and it is described briefly.     

Spernathecal morphology,sperm transfer and a novel mechanism of sperm displacement in the rove beetle,Aleochara curtula (Coleoptera,Staphylinidae)

Summary The mechanism by which sperm are transferred from the male's spermatophore to the female's storing cage is described for the rove beetle Aleochara curtula, emphasizing a novel mechanism of sperm displacement by competing males. The cuticular, U-shaped spermatheca is equipped with a valve structure and two sclerotized teeth. The tube of the spermatophore extends into the spermathecal duct through the guidance of the flagellum of the male endophallus. Further elongation of the spermatophore tube, however, occurs only after separation of the pair. A primary tube bursts at its tip after passing through the valve. Within the lumen of the primary tube, a second tube passes through the valve and continues to extend up to the apical bulb of the spermatheca, doubles back on itself and swells to form a balloon filling most of the spermatheca. The balloon of the spermatophore is pierced within the spermatheca by tooth-like structures pressed against the spermatophore through contraction of the spermathecal muscle. The same process of spermatophore growing and swelling is also observed in mated females. Sperm from previous copulations are backflushed through the valve and the spermathecal duct, indicative of last-male sperm predominance.Abbreviations ad adhesive secretion covering the sperm - sac am amorphous secretion of the spermatophore - as ascending portion of the spermatophore - ds descending portion of the spermatophore - end parts of the male endophallus - ext extended tube - f flagellum - gs genital segment - lt large tooth - m muscle of the spermatheca - nsc non sclerotized cuticle - op opening of the spermathecal gland - pt primary tube - sc sclerotized cuticle - sd spermathecal duct - se secretion of the spermathecal gland - sf secretion flowing out of the primary tube - sg spermathecal gland - sm sperm - smt small tooth - sp spermatheca - ss sperm sac - st secondary tube - vm vaginal muscle     

Description of the male reproductive system of Paguristes eremita (Anomura,Diogenidae) and its placement in a phylogeny of diogenid species based on spermatozoal and spermatophore ultrastructure

The male gonopores, male reproductive apparatus, spermatophore and spermatozoa of the Mediterranean hermit crab Paguristes eremita are described, using interference phase microscopy, scanning electron microscopy and transmission electron microscopy. A correlation is made between the gonopore morphology and the different kinds of setae accompanying them, and the reproductive biology of these crabs. Each testes merges into a tubular duct made up of four zones: (1) the collecting tubule with free spermatozoa; (2) the proximal zone, where the ampulla of the spermatophores starts to be formed; (3) the medial zone, where the ampulla is completed, the stalk lengthens and the pedestal is formed; (4) the distal zone, where the mature spermatophores are stored. The sizes of the different parts of the spermatophore and of the sperm are given and their exterior morphology and ultrastructure described and compared to congeners. The morphology of the gonopore, male reproductive system, spermatophore and spermatozoa of P. eremita are species-specific, clearly distinguishing the species from the other members of the family. The available spermatozoal and spermatophore data is used to place P. eremita within a sperm phylogeny of the hermit crab family Diogenidae.     

Mating in the Scaly Cricket Cycloptiloides canariensis (Orthoptera: Gryllidae: Mogoplistinae)

The process of mating in C. canariensis follows basically the same pattern as in other crickets: adoption of the female-above-male position, hooking of the male onto the female's subgenital plate, spermatophore transfer, and separation of the mates. Two crucial modifications can, however, be distinguished: Hooking is not accomplished by means of a sclerotized process from the protruded epiphallus, but with paired hooklets on the paraproct (paraproct processes; sternite 11). The paraproct processes are about 0.4 mm long and covered with bristles, and a group of campaniform sensilla is found in the tip region. The time course of copulation is also modified. Usually, in crickets an already fully formed spermatophore is transferred immediately after mounting, and remains attached for a considerable period. C. canariensis, however, needs about 15 min for spermatophore production, while the couple is already hooked. After transfer the spermatophore remains attached only for an average of 31 s. With both hooklets severed, copulation is unsuccessful. Severance of only one hooklet prolongs the initial hooking phase but shortens the following interval, which suggests that spermatophore production is triggered during a definite interval before hooking, and continues as an autonomous internal process.     

Cumulative Effect of Male's Displays in the Sexual Behaviour of the Smooth Newt Triturus vulgaris (Urodela,Salamandridae)1

The relevance of the temporal spacing of signals to the timing and nature of the receiver's response during a communicative process was studied in the sexual behaviour of the smooth newt Triturus vulgaris. The possibility that a high rate of stimulation allows an accumulation of the effects of successive signals was investigated by comparing sexual interactions leading and not leading to spermatophore deposition. Results showed that the difference between the two types of interactions lay only in temporal features of the stimulation provided by the male to the female. Females, although in a comparable initial state of receptivity and exposed to comparable amounts of stimulation, performed the act triggering spermatophore deposition by the male only in some interactions. Display bouts, in which the male displayed at short intervals (less than 4 s), were longer in interactions where spermatophore deposition took place than in the others. This suggests that courtship was effective if accumulation of the effects of male displays could occur. This proposition was supported by the observation of a progressive change in the immediate female response to a given male display in the group where courtship bouts were longer. Our results indicate the existence of a system of tonic communication (see Schleidt 1973) during the sexual behaviour of the smooth newt, in which the effects of the male displays accumulate over time until some critical threshold is reached in the female.     

Spermatogenesis and spermatophore production in the hawaiian red lobster Enoplometopus occidentalis (Randall) (Crustacea,nephropidae)

Light microscopy of the male reproductive tract of the Hawaiian red lobster Enoplometopus occidentalis documented the cyclic nature of spermatogenesis and spermatophore formation. Testes are composed of a convoluted collecting tubule bearing many spermatogenic follicles, all within a supporting mesentery. Spermatogonia are restricted to the basal side of the follicular epithelium and proliferate at onset of spermateleosis within the same follicle. Two generations of spermatogenic cells thus occupy each follicle, and accessory cells in the follicle form a basophilic epithelium between them. These accessory cells may detach with the spermatozoa at spermiation. The vas deferens lies outside the testicular mesentery and consists of a coiled proximal portion in which spermatophore production commences. Clusters of spermatozoa are here surrounded by a PAS-positive primary spermatophore layer, and a PAS-negative outer bounding layer is initiated. Completed further distally in the vas deferens, the outer bounding layer is thinner on the side of the spermatophore which adheres to the substratum after ejaculation; the thick side of this layer forms a broad cap. Outer circular and inner longitudinal muscular layers become well developed in the distal loop and descending portions of the vas deferens. The terminal portion of this duct contains no spermatophore prior to ejaculation. It has a longitudinally folded epithelium and an attached tubular gland which produces an extra-spermatophoral, gelatinous secretion. The androgenic gland is associated with this terminal segment of the vas deferens. These features are compared with those reported for other lobsters.     

Structural changes in the spermatophore of the freshwater 'red claw' crayfish Cherax quadricarinatus (Von Martens, 1898) (Decapoda, Parastacidae)

López Greco, L.S. and Lo Nostro, F.L. 2007. Structural changes in the spermatophore of the freshwater ‘red claw’ crayfish Cherax quadricarinatus (Von Martens, 1898) (Decapoda, Parastacidae). —Acta Zoologica (Stockholm) 88 : 000–000 The structure of the spermatophore was studied in Cherax quadricarinatus. Pieces of the distal vas deferens and transferred spermatophore from the females were fixed, cut and stained. Within the distal vas deferens, the primary layer and the secondary layer of the spermatophore were distinguishable. In the latter, two components were detected: cytoplasmic droplets and a homogeneous matrix. During the first 10 minutes post‐extrusion the cytoplasmic droplets drastically changed from looking like ‘empty droplets’; at this time the spermatophore changed from a liquid stage to a sticky one. One hour after extrusion the spermatophore began to harden and within the first 24–48 h post‐mating it was a solid and intense white structure tightly attached to the female; after 72 h it acquired a softer aspect, completely dehiscing between 96 and 120 h post‐mating. Histologically, the primary layer maintained its integrity surrounding the spermatozoa while the secondary layer lost the cytoplasmic droplets. The spermatophore began to hydrate between 24 and 48 h and by 72–96 h many sections of the sperm cord began to coalesce. From 48 h post‐mating some fissures appeared within the matrix that enlarged between 72 and 120 h. We propose that both manipulation by the female and hydration are the mechanisms involved in the release of the spermatozoa from the spermatophore.     

Chemical induction of mating abnormalities and spermatophore production in the Mediterranean flour moth, Ephestia kühniella

Hexamethyl-melamine (hemel) when injected into male Ephestia kühniella induced mating aberrations expressed as permanent copulation, sterile mating and spontaneous production of spermatophore. Permanent copulation was not caused by blockage or an elongated spermatophore column but probably caused by failure of the male reproductive organs to completely transfer the spermatophore. Spontaneous spermatophore formation was induced by both cholinesterase inhibitors and nerve stimulants, the effect of the former being more pronounced. It was not caused by stress due to poisoning since DDT even at lethal doses did not induce a response. The results suggest involvement of the nervous system in spermatophore production during a normal mating.     

Ultrastructure and functional morphology of the female reproductive organs inProtodrilus (Polychaeta,Annelida)

The morphology and function of the female reproductive organs in 6Protodrilus species are investigated by light- and transmission electron microscopy. Possible ways in which spermatozoa may enter the female coelom after leaving the spermatophore are discussed for species with and without special female reception organs. Only femaleP. rubropharyngeus andP. flavocapitatus have “dorsal organs” for spermatophore reception. The structure and function of these organs are described, as well as those of the oviduct found in 3 of the species investigated. The possible phylogenetic origin of gonoducts and different modes of oviposition within the genus are discussed. Finally, the high taxonomic significance of female traits such as dorsal organs, oviducts, cocoon glands and lateral ciliary rows in this genus is stressed.