Redescriptions of Phallodrilus parthenopaeus Pierantoni and P. obscurus Cook (Oligochaeta, Tubificidae)

The type species of Phallodrilus Pierantoni, 1902, P. parthenopaeus Pierantoni, 1902; is redescribed on the basis of new material from W Scotland. The species is characterized by its specific spermathecal and penial setae, its very slender atria, and its long spermathecal ducts. Sexually fully mature specimens of P. obscurus Cook, 1969 are described for the first time, on the basis of material from New Jersey (E USA). The new material shows that this species possesses 5 to 9 penial setae in each ventral bundle of segment XI, and that its atria are coated with a relatively thick musculature.     

A new earthworm species of the genus Drawida Michaelsen(Oligochaeta: Moniligastridae) from China

A new species of terrestrial earthworms is described as Drawida dandongensis sp. nov. from Dandong, Liaoning, China. It is distinguished from others by a pair of spermathecal pores lie in the ventral of 7/8 intersegmental furrow, and a pair of male pores lie in 10/11 intersegmental furrow, between setae b and c.     

Nine new species of Dichogaster (Oligochaeta, Megascolecidae) from Guadeloupe (French West Indies)

Nine species belonging to two distinct groups within the genus Dichogaster Beddard, 1888 are described from material collected on the volcanic section of the island of Guadeloupe. The species Dichogaster arborea, D. caesitifusca, D. callaina, D. girija and D. basseterrensis all inhabit the leaf tanks of bromeliads and share the following anatomical characteristics: spermathecal pores on the trailing edges of segments, spermathecal axis differentiated into ampulla, internally fluted central chamber and duct, penial setae long and slender, testes and funnels free, prostomium undivided or divided by two grooves, simple single typhlosole and a pair of dorsal caeca on the mid-intestine. Dichogaster athena also inhabits bromeliads, but lacks the above characteristics and male reproductive organs, and is more similar to the remaining species. The three remaining species, D. guadeloupensis, D. matoubensis and D. musciphila , with lateral typhlosoles, no intestinal caeca, simpler spermathecal structure, prostomiums divided by a single groove and short penial setae, all inhabit soils of montane forests. The division of Dichogaster based on muscularity of the proventriculus wall is shown to be unsupportable, since thickness of the wall is size-related.     

Six new species of marine Tubificidae (Oligochaeta) from the continental shelf off Peru

Six species of marine tubifieids are described from the continental shelf off Peru. Two of them are members of the gutless genus Olavius Erséus, 1984 (subfamily Phallodrilinae). Olavius bullatus sp.n. possesses 2 pairs of large penial setae in voluminous copulatory sacs, tiny atria, and spermathecal pores in line with dorsal setae. Olavius crassitunicatus sp.n. is characterized by small atria with thin muscular layer, spermathecae with short ducts, opening dorso-laterally, and lack of penial setae. Four species arc members of the subfamily Limnodriloidinae. Limnodriloides busilicus sp.n. belongs to the appendiculatus-group (sensu Erséus). It is discriminated by somatic setae with subdental ligaments, and its voluminous elongate prostatic pads. Limnodriloides clavellatus sp.n. is distinguished from its congeners by a peculiar bulge in the cavity of each atrial ampulla, and spermatozeugmata imbedded in the walls of the spermathecae. Tectidrilus intermixtus sp.n. is similar to T. bori (Righi & Kanner, 1979); it is distinguished from the latter by having trisetal bundles in segment V or V-VI and by lacking copulatory glands. Marcusaedrilus peruanus sp.n. is characterized by nongranulated atrial ducts and bipartite spermathecae.     

双蜺腔蚓的生殖器官多态现象（寡毛纲：巨蚓科）

报道腔蚓属Ｍｅｔａｐｈｉｒｅ蚯蚓Ｍｅｔａｐｈｉｒｅｆａｎｇｉ（Ｃｈｅｎ,１９３６）及Ｍｅｔａｐｈｉｒｅｂｉｐａｐｉｌｌａｔａ（Ｃｈｅｎ,１９３６）应作为Ｍｅｔａｐｈｉｒｅｂｕｃｃｕｌｅｎｔａ（Ｇａｔｅｓ,１９３５）的同种异名,并记述该种的生殖器官多态现象。     

Propappidae and aquatic Enchytraeidae (Oligochaeta) from the farthest southeast of Russia

Two mountain streams north and northeast of Vladivostok were studied in 1983–1984. In the Komarovka Stream, a great variety of Mesenchytraeus occurred in the spring zone, among them M. crenobius sp. n. with giant setae in the ventral bundles of VI–VIII and M. vshivkovae sp. n. with numerous spermathecal diverticula. In the stream zone of the Frolovka Stream Cernosvitoviella pensau sp. n., characterized by a complicated penial bulb and a very long spermathecal ampulla, was the dominant oligochaete. Propappus arhynchotus Sokolskaya was the second most abundant oligochaete in this stream. It proved to be a true member of this genus and not synonymous with any other species. These are the first records of aquatic enchytraeids for the Primorski Region of Russia.     

Tubificidae (oligochaeta) from the Ross Sea (Antarctica), with descriptions of one new genus and two new species

Three species,Torodrilus gelidus sp. nov. (subfamily Rhyacodrilinae),Rossidrilus terraenovae gen. et sp. nov. (Limnodriloidinae), and a second unnamed species of Limnodriloidinae, are reported from marine sediments in Terra Nova Bay, Ross Sea. Torodrilus gelidus is distinguished fromT. lowryi Cook, 1970 by its setal pattern (with few exceptions, both anterior and posterior setae are single-pointed in sexually mature specimens ofT. gelidus) and the morphology of its male protuberances (the latter folded over a midventral bursa in segment XI).Rossidrilus terraenovae is characterized by large diverticula attached to the oesophagus in the posterior part of segment IX, unpaired male and spermathecal pores, heavily muscular and entally ciliated atrial ampullae, elongate prostatic pads, and a deep, unpaired and muscular, copulatory sac. It is the first species of its subfamily to be described from Antarctic waters.     

A newly discovered sperm transport system in the female of Lygaeidae bugs

In the female reproductive system of the relatively large hemipteran, the western conifer seed bug Leptoglossus occidentalis (Heidemann), a cuticle‐lined tube extends medially along the surface of the vagina from the proximal end of the spermathecal complex anteriorly to the base of the common oviduct. This medial tube houses the proximal end of the spermathecal duct, thereby enabling the transport of material from the spermatheca at the distal end of the spermathecal complex, past the vagina (or bursa copulatrix) and directly to the common oviduct. The proximal portion of the spermathecal complex also contains an insemination duct that is separate from the spermathecal duct. The insemination duct allows the male intromittent organ to extend from the vagina to the spermatheca without navigating through the spermathecal duct. The reproductive systems of two previously studied Hemiptera, the milkweed bug Oncopeltus fasciatus (Dallas) and the box elder bug Leptocoris trivittatus (Say), possess a similar cuticle‐lined medial tube housing the spermathecal duct. This new information provides a clearer understanding of sperm transport in the female reproductive system of Lygaeidae bugs, and helps to clarify the path of the male organ during copulation, as well as the movement of sperm during egg laying.     

Sperm aggregations in the spermatheca of the red back salamander (Plethodon cinereus)

The spermatheca of Plethodon cinereus is a compound tubular gland that stores sperm from mating in early spring (March–April) to oviposition in summer (June–July). The seasonal variation of sperm storage in this species has previously been studied by light and transmission electron microscopy. In this paper, sperm aggregations, interaction of sperm with the spermathecal epithelium, and spermathecal secretions are studied using scanning electron microscopy. Within spermathecal tubules, relatively small groups of sperm are aligned along their entire lengths in parallel arrays. This pattern is similar to other plethdontids with complex spermathecae. Lumina of spermathecal tubules are filled with secretory material in April prior to the arrival of sperm, and after sperm appear, a coating of secretory material persists on the apices of the spermathecal epithelium. Sperm peripheral to the central luminal mass can become embedded in the secretory matrix or pushed deeper into the spermathecal epithelium. The spermathecal secretions may serve to attract and prolong the viability of sperm, but sperm that become enmeshed in the secretions or epithelium are phagocytized. Sperm and spermathecal secretions are largely absent after ovulation and in summer months, and new secretory vacuoles are formed in fall, although mating does not occur until spring.     

Two new species of freshwater Oligochaeta from the North-west Iberian Peninsula: Krenedrilus realis sp. nov. (Tubificidae) and Cernosvitoviella bulboducta sp. nov. (Enchytraeidae)

Two new species of aquatic Oligochaeta are described from the North-west Iberian Peninsula: Krenedrilus realis sp. nov. (Tubificidae) and Cernosvitoviella bulboducta sp. nov. (Enchytraeidae). Krenedrilus realis is the fourth species in a genus of small and presumably plesiomorphic Tubificinae. It is closely related to K. sergei Giani, Erséus & Martínez-Ansemil, 1990. Cernosvitoviella bulboducta belongs to a genus of small amphibiotic enchytraeids. It is close to C. ampullax Klungland & Abrahamsen, 1981 and C. tatrensis (Kowalewski, 1916). Supplementary data to the diagnosis of C. tatrensis are given. The presence of two small glands attached to the gut immediately behind the pharyngeal bulb is noticed in C. bulboducta and C. tatrensis . This previously unknown character is probably more common in the genus than has been supposed.     

Structure and function of the spermathecal complex in the phlebotomine sandflyPhlebotomus papatasi Scopoli (Diptera: Psychodidae): I. Ultrastructure and histology

Females of phlebotomine sandflies (Diptera: Psychodidae) possess highly variable spermathecae that present several important taxonomic characters. The cause of this diversity remains a neglected field of sandfly biology, but may possibly be due to female post-mating sexual selection. To understand this diversity, a detailed study of the structure and function of the spermathecal complex in at least one of the species was a prerequisite. Using scanning and transmission electron microscopy, described here is ultrastructure of the spermathecal complex in the sand fly,Phlebotomus papatasi Scopoli. The spermathecal complexes are paired; each consists of a long spermathecal duct, a cylindrical spermathecal body, and a spherical spermathecal gland. Muscle fibres, nerves, tracheoles, and vascular sinuses connect the spermathecal body and duct through the epithelial layers. Spermathecal gland is formed by a typical insect epidermis and consisting of an epithelial layer of class-1 epidermal cells and elaborate glandular cells of class-3 epidermal cells, each having both receiving and conducting ductules (i.e. “end apparatus”) and a “cytological apodeme”, which is a newly described cell structure. The spermathecal body and duct are lined by class-1 epidermal cells and a cuticle, and are enveloped by a super-contracting visceral muscular system. The cuticle consists of rubber-like resilin, and its fibrillar arrangement and chemical nature are described. A well-developed neuromuscular junction exists between the spermathecal gland and the spermathecal body, which are connected to each other by a nerve and a muscle. The spermathecal complexes of the sandfly are compared with those of other insect species. The physiological role and possible evolutionary significance of the different parts of spermathecal complex in the sandfly are inferred from the morphology and behaviour. Post-mating sexual selection may be responsible for the structural uniqueness of the spermathecal complex in phlebotomine sandflies.     

Function of the spermathecal muscle in Chelymorpha alternans Boheman (Coleoptera: Chrysomelidae: Cassidinae)

Abstract. When the spermathecal muscle of a virgin female Chelymorpha alternans Boheman (Coleoptera: Chrysomelidae) was cut, the number of spermatozoa transferred in a single mating to the spermatheca and the spermathecal duct was not affected, but their distribution differed. Cutting the spermathecal muscle also reduced egg fertility. Eggs from females with a cut muscle showed a lower average percentage fertilization. Longer delays in oviposition after removal of the spermathecal muscle were associated with higher proportions of infertile eggs.     

Ecological and morphological attributes of parthenogenetic Japanese Schwiebea species (Acari: Acaridae)

We examined life history traits and spermathecal morphology of both sexual and thelytokous Schwiebea mite species to determine ecological and morphological attributes during the evolution of parthenogenesis in this lineage. We reconstructed a molecular phylogeny of eight Japanese species using the internal transcribed spacer 1 (ITS1) of the ribosomal DNA (rDNA) and compared the sex ratio, developmental period, and egg number (fecundity) of each species within a species group by rearing them in the laboratory. Habitat preference was also analyzed from both collection and literature data. The reconstructed molecular phylogeny suggested that parthenogenesis evolved independently multiple times in this lineage. There were three clusters in the tree, in each of which the idiosoma, leg, setae, and spermathecal morphology of females was similar or identical; this suggested that mites in the same cluster were sister species. There was no relationship between sexual mode and life history traits or habitat preference. These results suggest that sexual and asexual species use different microhabitats. Because S. similis (sexual), S. elongata (thelytokous), and S. estradai (thelytokous) were in the same cluster and spermathecae of the first two were similar while that of the last was distinctively reduced, we hypothesized that speciation occurred in this order and that spermathecae are reduced and eventually lost during the course of parthenogenetic evolution.     

Functions of the spermathecal muscle of the boll weevil,Anthonomus grandis

In female boll weevils, Anthonomus grandis, spermathecal filling was not affected by severing the spermathecal muscles. Females whose spermathecal muscles were severed 2 to 4 weeks after mating laid infertile eggs and resumed virginal ovipositional behaviour indicating the importance of this muscle in supplying sperm for egg fertilization. The presence of normal active sperm within the spermatheca in no way influenced ovipositional behaviour. In females whose spermathecal muscles had been severed, 22 per cent sperm displacement occurred after a second mating compared with 66 per cent for normal females. The physical displacement of sperm was thus largely dependent on a functional spermathecal muscle.     

Taxonomic Revision of the Marine Genus Heterodrilus Pierantoni (Oligochaeta,Tubificidae)1

Marine tubificids possessing trifid anterior setae are morphologically and taxonomically reviewed, on the basis of material from the Atlantic and Pacific Oceans. Heterodrilus Pierantoni, 1902 is revised to include thirteen species, H. arenicolus Pierantoni, 1902, H. minisetosus sp.n.H. ascensionensis sp.n. H. queenslandicus (Jamieson, 1977), H. lacertosus sp.n. H. scitus sp.n. H. keenani sp.n. H. claviatriatus sp.n. H. subtilis (Pierantoni, 1917), H. jamiesoni sp.n. H. occidentalis sp.n. H. pentcheffi sp.n. and H. bulbiporus sp.n. The genus is briefly defined: marine tubificids with trifid setae in preclitellar segments (with H. subtilis as the only exception); paired spermathecae located in segment X; vasa deferentia entering apical, ental ends of slender, ciliated atria, which bear broadly attached masses of prostate glands; paired male pores, and generally with penial setae arranged in bisetal bundles. Heterodriloides gen.n. is established for H. quadrithecatus sp.n. distinguished from Heterodrilus by two main features: its spermathecae are located in XII, with a supplementary pair generally located in XI; and its vasa enter the ectal part of the atria. Giereidrilus gen.n. a third genus with trifid setae, is established to include Phallodrilus ersei Giere, 1979 and G. inermis sp.n. Both species have unpaired spermathecal and male pores, and their atria are not ciliated. Heterodrilus, Heterodriloides and Giereidrilus are placed in the subfamily Rhyacodrilinae Hrabě, 1963.     

Coevolution of male and female genitalia in stalk-eyed flies (Diptera: Diopsidae)

The present study investigates the coevolution of a particular male genital process and the female spermathecal ducts in a clade of stalk-eyed flies (Diptera, Diopsidae) and debates the underlying evolutionary mechanisms. The fine morphology and interaction of the male and female genitalic structures are reconstructed from serial sections of mating pairs in one of the species. It is found that the male genital process traverses the common spermathecal duct to enter the base of one of the separate spermathecal ducts during the mating. Spermatozoa and accessory secretions are not transferred through the male genital process but can be discharged only from the male gonopore near its base. A detailed morphometric study reveals low intraspecific variation and hypoallometry of the male genital process. Across 17 species studied comparatively, the lengths of the male genital process and the female common and separate spermathecal ducts are highly variable. The length of the male genital process is correlated significantly with that of the female common spermathecal duct, but not with that of the separate spermathecal ducts. Based on the combined evidence it is concluded that the male genital process and the female common spermathecal duct have coevolved, and that sexual selection by cryptic female choice constitutes a possible and parsimonious explanation for their coevolution. Alternative or additional explanations in terms of sexually antagonistic coevolution cannot be ruled out conclusively, but are not supported by the available evidence.     

PAR-3 is required for epithelial cell polarity in the distal spermatheca of C. elegans

PAR-3 is localized asymmetrically in epithelial cells in a variety of animals from Caenorhabditis elegans to mammals. Although C. elegans PAR-3 is known to act in early blastomeres to polarize the embryo, a role for PAR-3 in epithelial cells of C. elegans has not been established. Using RNA interference to deplete PAR-3 in developing larvae, we discovered a requirement for PAR-3 in spermathecal development. Spermathecal precursor cells are born during larval development and differentiate into an epithelium that forms a tube for the storage of sperm. Eggs must enter the spermatheca to complete ovulation. PAR-3-depleted worms exhibit defects in ovulation. Consistent with this phenotype, PAR-3 is transiently expressed and localized asymmetrically in the developing somatic gonad, including the spermathecal precursor cells of L4 larvae. We found that the defect in ovulation can be partially suppressed by a mutation in IPP-5, an inositol polyphosphate 5-phosphatase, indicating that one effect of PAR-3 depletion is disruption of signaling between oocyte and spermatheca. Microscopy revealed that the distribution of AJM-1, an apical junction marker, and apical microfilaments are severely affected in the distal spermatheca of PAR-3-depleted worms. We propose that PAR-3 activity is required for the proper polarization of spermathecal cells and that defective ovulation results from defective distal spermathecal development.     

The spermathecal complex in Ips typographus (L.): Differentiation of the spermathecal gland related to age and reproductive state

The spermathecal complex of the bark beetle, Ips typographus, comprises the following elements: spermathecal duct, spermatheca and spermathecal gland. The spermathecal duct connects the vagina and the spermatheca and consists of a cuticular tube surrounded by an epithelial layer and circular muscles. The spermatheca is bottle-shaped and has a cuticle-lined lumen. Muscles are attached to both ends of the spermatheca. The spermathecal gland which is connected to the spermatheca possesses three cell types: glandular, hypodermal, and ductule. The glandular cells have different structural characteristics depending on the age and reproductive state of the females. After the emergence of the brood, two different kinds of secretory material are present in the glandular cells. There is evidence that one type of secretion is emitted during the first few days after brood emergence, while the other type accumulates to be secreted during later stages.     

The rôle of the spermathecal gland of the boll weevil,Anthonomus grandis

Spermatozoa were relatively inactive and did not enter the spermatheca of female boll weevils, Anthonomus grandis, whose spermathecal glands were removed as teneral adults. However, these females were able to lay fertile eggs for a 2 week period. When the spermathecal gland was removed from older females, spermathecal filling occurred, and although the spermatozoa retained their fertilizing capacity for extended periods, spermathecal emptying did not occur. Spermatozoa gradually lost their motility and fertilizing capacity, indicating that spermathecal secretions are effective in very small amounts. Spermatozoa were not activated by any of the materials contained in the normal male ejaculate. These materials alone did not effect spermathecal filling nor were they capable of maintaining the fertilizing capacity of the spermatozoa for very long. Sperm economy is low with less than 1 fertile egg laid per 100 spermatozoa used.