Ultrastructure of the spines in the copulatory organ of some Monocelididae (Turbellaria,Proseriata)

Summary A comparative ultrastructural study of the copulatory organ was carried out in four genera of Turbellaria-Monocelididae. In all four genera the male copulatory organ is of the conjuncta-duplex type and has a cirrus armed with spines. Fine-structural analysis of the cirrus spines reveals that these structures are specializations within the basement lamina of the cirrus. In this part of the male canal the basement lamina has a trilamellar structure. The spines are formed by a local thickening of the middle electron-dense layer and show a structural similarity in all the Monocelididae investigated.The systematic value of this character within the family Monocelididae is discussed.Abbreviations b bacteria - bl basement lamina - cr cell remnants - g granules of prostate glands - hd hemidesmosomes - l lumen of cirrus - m _c muscles of cirrus - m _b muscles of bulbus - mi mitochondria - p parenchymal elements - s spine - sp septum - st stylet - sz spermatozoa     

Fasciola hepatica: the ultrastructure of the epithelium of the seminal vesicle, the ejaculatory duct and the cirrus.

The ultrastructure of the seminal vesicle, ejaculatory duct, cirrus sac and cirrus is described. The epithelium of the seminal vesicle consists of a single layer of squamous to cuboidal cells. The apical ends of the cells have thin polymorphic lamellae and long narrow pits, both of which enclose normal spermatozoa. The cells have a moderate amount of GER and Golgi complexes which produce a lucid secretory body. The ejaculatory duct epithelium is composed of cuboidal to columnar cells between or through which project the terminal parts of the ducts of the unicellular prostate glands. The apical surfaces of the epithelia are extended into triangular or filiform projections having thin sinuous lamellae. The cytoplasm contains GER cisternae and Golgi complexes which synthesize a dense ovoid secretion. The cirrus sac and cirrus are covered by a thin modified tegument. The cirrus has many spines and the normal ratio of T1 and T2 type of secretory bodies, whereas the cirrus sac has few spines and the T2 type of secretory body predominates over the T1 type. The significance and possible functions of the structures observed in the three tissues are discussed.     

Ultrastructure of the copulatory organ of Haplopharynx quadristimulus and its phylogenetic significance (Plathelminthes,Haplopharyngida)

Summary The male reproductive system in Haplopharynx quadristimulus consists of paired testes, sperm ducts, seminal vesicles, seminal ducts, a copulatory organ containing prostatic vesicle and stylet apparatus, and the male canal. By electron microscopy all components appeared to be regional specializations of a canal extending from the testes to the body wall and lined by a multiciliated epithelium. The epithelium of the stylet apparatus contained six different cell types. One cell type (matrix syncytium) formed the stylet and the other five were located distal to the stylet/prostatic-vesicle junction along the male system epithelium. Each cell type was attached to the supporting intercellular matrix at a different level along the stylet apparatus. All cell types extended to the distal end of the stylet apparatus regardless of where they originated along its length. The cells in the apparatus lacked cilia, but one of the cell types contained rootlets. Modified rootlets or rootlet derivatives were possibly present in another cell type in the form of rootlet-like ribbons. The findings support the monophyly of the Macrostomida Haplopharyngida (by common occurrence of a matrix syncytium) and at the same time suggest their separation as two distinct taxa (by differences in the structure of the prostatic vesicle and other parts of the stylet apparatus).Abbreviations a accessory spine - c circular muscle - ce centriole - ci cilium - di dictyosome - e epithelial cell - ed ejaculatory duct - ep epidermal cell - f rootlet-like ribbon - g prostatic gland cell neck - g1 type I gland cell granules - g2 type II gland cell granules - g3 type III gland cell granules - h hemidesmosome - i intercellular matrix - im internal muscle - j septate junction - l stylet apparatus lumen - le spine lateral extension - lm longitudinal muscle - m matrix syncytium - mc male-canal epithelial cell - me male canal - mp male pore - mt microtubules - mv microvilli - n nucleus - nc nerve cell body - np nerve process - om oblique muscle - p prostatic vesicle epithelial cell - pv prostatic vesicle - r rootlet - s stylet - sa stylet apparatus - sc sensory receptor - sd sperm duct - se seminal duct - sl stylet lumen - sp spot desmosome - sr sperm - sv seminal vesicle - t terminal web - te testis - u ultrarhabdite - z zonula adhaerens - 2 cell type 2 - 3 cell type 3 - 4 cell type 4 - 6 cell type 6     

Development of the reproductive apparatus of the land planarian Rhynchodemus sylvaticus (Turbellaria: Tricladida) and its significance for classification in the genus

Seven specimens of Rhynchodemus sylvaticus (Leidy) collected from a variety of localities in the US and having variously developed copulatory organs are believed to represent stages in the development of the copulatory apparatus. Four specimens were juveniles with under-developed male components, one specimen had a well-developed female atrium and small male component, and two specimens were mature with a male organ twice the size of the female part. In early stages, the male component had sperm ducts, seminal vesicle, and narrow atrium; more mature stages had a considerable elongated atrium with thick folds in its muscularized wall, a massive muscular bulbus; and a sigmoid ejaculatory duct opening into the large bulbar cavity. Morphological features of mature male copulatory organs in all species of the genus Rhynchodemus are basically similar whereas external body features (color and number of dorsal stripes) of these same species differ.     

Ultrastructure of the cirrus sac of echinophallid tapeworms (Cestoda, Bothriocephalidea) and the terminology of cirrus hard structures

Transmission (TEM) and scanning (SEM) electron microscope methods were used to study the fine structure of the cirrus, cirrus sac, internal seminal vesicle, ejaculatory duct, prostate glands and cirrus armature of Echinophallus wageneri (Monticelli, 1890) and Paraechinophallus japonicus (Yamaguti, 1934) (Bothriocephallidea: Echinophallidae). The cirrus sac of these species has two unique ultrastructural features: a thick wall with two bands of muscles and prominent, rooted hard structures. Rare traits echinophallids share with diphyllobothriideans are microtriches on the ejaculatory duct and with spathebothriideans, well-developed unicellular prostate glands outside the cirrus sac. Because there is a similarity of cirrus armature and rostellar hooks in having a tegumental localisation and in having a heterogenous structure of the blade and root, a cortex, a central pulp region and a recurved apex, these structures are named “modified hooks” instead of spines. They also have a spiral arrangement; no base plate was observed. True spines, as found in trematodes, are between the surface and basal plasma membrane of the external syncytial layer of the tegument, rest on the basal plasma membrane of the distal epithelial cytoplasm, show a homogeneous electron-dark crystalline appearance and are covered by the surface plasma membrane. Aside from the characteristic hooks on the scolex of various cestodes, we see no evidence that would preclude the development of still other specialised structures, such as these modified hooks, from microtriches. In spite of the absence of studies on the development of modified hooks from the cirrus of echinophallids and/or its consideration as derived from microtriches, we assume that like microtriches, formation of modified hooks is from tegumental bodies and therefore they are derivative structures of the cestode tegument.     

Developmental sequence for the copulatory organs of Kontikia mexicana with remarks on taxonomic significance (Turbellaria: Tricladida: Geoplanidae)

Five specimens, presumably representing different developmental stages of the land planarian Kontikia mexicana (Hyman, 1939), were used to reconstruct the development of the copulatory apparatus in this species. The results support the notion that Kontikia differs from the closely related Caenoplana in its possession of a penis papilla. In the earliest stage available, a penis papilla was absent and other components were not differentiated. In a late-juvenile condition, the gonopore, seminal vesicle, and ejaculatory duct were present. The short penis papilla appeared to arise in this stage by elongation of the terminal tissue around the ejaculatory duct and its separation from the antral wall. The female canal was guarded by an epithelial fold and the glandular duct was present. In the mature condition, the penis papilla was more elongate, and the secretory (prostatic) region of the ejaculatory duct was functional. The female canal, guarded by an epithelial fold, was well-developed with enlarged glandular duct but lacking the posterior diverticulum and the sperm storage system associated with the ovovitelline ducts known in Kontikia orana Froehlich, 1955.     

Comparative ultrastructure of copulatory organs having a stylet in the Proseriata (Turbellaria)

The ultrastructure of male copulatory organs having a stylet has been studied in some genera of the Proseriata.Within the Monocelididae there was a variety of stylet-like hard structures. The stylet in Monocelis fusca was a differentiation of the basement membrane of the epithelium lining a penis-like muscular papilla. The penis papilla in Ectocotyla consisted of circular muscles surrounded by a thickened basement membrane and an epithelium. Archilopsis sp. and Archilina sp. with a duplex copulatory bulb, had a stylet within a spiny cirrus. The stylet in Archilopsis sp. was a cylindrical muscular protrusion with a thickened basement lamina that lined the cirrus lumen. The stylet structure in Archilina sp. was composed of four long spines which were derivatives of the basement membrane. In Ectocotyla multitesticulata and Dupliminona corsicana, the accessory prostatoid organ was provided with a hook-shaped stylet that was differentiated in the basement membrane and of which the material was continuous with the fibrous matrix between the muscles of the prostatic bulb. The stylet and needles in the Archimonocelis species were intracellular differentiations. The copulatory organ in Carenscoilia biforamen consisted of a tubiform stylet and four needles, all of which were also intracellular specializations.I consider copulatory hard structures in the Turbellaria to be taxonomically significant in terms of structure, differentiation, and location (whether subcellular, in the basement membrane, or intracellular).     

Blood flukes (Digenea: Aporocotylidae) of stingrays (Myliobatiformes: Dasyatidae): Orchispirium heterovitellatum from Himantura imbricata in the Bay of Bengal and a new genus and species of Aporocotylidae from Dasyatis sabina in the northern Gulf of Mexico

We redescribe Orchispirium heterovitellatum based on the holotype and 3 original voucher specimens collected from the mesenteric blood vessels of scaly whiprays Himantura imbricata (Bloch and Schneider, 1801) (as Dasyatis imbricatus) captured in the western Bay of Bengal off Waltair, India. We emend the diagnosis of Orchispirium to include anterior sucker present, testis looping, cirrus sac enveloping large internal seminal vesicle, oviducal seminal receptacle present, and metraterm short and thin-walled. We describe Myliobaticola richardheardi n. gen., n. sp. based on live observations, light microscopy, and scanning electron microscopy of adult specimens collected from between the cardiac trabeculae of Atlantic stingrays Dasyatis sabina (Lesueur, 1824) captured in Mississippi Sound (type locality), Mississippi, and Apalachicola Bay, Florida. The new species has a minute, aspinous body lacking lateral tubercles; an aspinous and eversible anterior sucker lacking a peduncle; a posterior esophageal swelling; an inverse U-shaped intestine; smooth ceca terminating in the anterior body half; a looping testis lacking lobes; a cirrus sac enveloping a large internal seminal vesicle; a medial and primarily post-testicular ovary; an oviducal seminal receptacle; a postgonadal uterus flanking the internal seminal vesicle; a short and thin-walled metraterm; and a common genital pore. It lacks a pharynx and Laurer's canal. No other named aporocotylids infect a member of cohort Batoidea or have the combination of an aspinous body, an aspinous anterior sucker, a posterior esophageal swelling, an inverse U-shaped intestine, a looping testis, a cirrus sac enveloping a large internal seminal vesicle, and a common genital pore; these observations indicate that O. heterovitellatum and M. richardheardi are closely related. The discovery of a second species representing a second genus of Aporocotylidae in diamond stingrays (Dasyatidae) suggests that Batoidea is an undersampled host group for aporocotylid infections.     

Sand dwelling Turbellaria from the Netherlands Delta area

Sand dwelling Turbellaria from the Delta of the Rivers Rhine, Meuse and Scheldt have been investigated. Thirty-eight samples taken from littoral and sublittoral stations in the Grevelingen, Eastern and Western Scheldt have been analysed.Thirty-three species were recorded (Acoela were not considered); twenty-four of them are new for the area and seven new species are described.Density and diversity of Turbellaria were higher in the Eastern Scheldt than in the Western Scheldt or in the Lake Grevelingen. A maximum density of 82 ind./100 cm³ was noted. A tentative calculation on relative abundance of the representatives of the different Turbellaria orders is established. Proseriata seem to be dominant in the localities studied.Abbreviations acg : accessory glands - aco : accessory organ - ad : atrial diverticle - b : bursa - br : brain - cil : cilia - cm : circular muscle - cn : cnidosac - co : copulatory organ - cs : cuticular spines - css : cuticular stylet sheat - de : ejaculatory duct - di : ductus intervesicularis - ds : seminal duct - dsp : spermatic duct - en : enteron - fd : female duct - fp : femal pore - ga : genital atrium - gf : glands in female duct - gg : glands - gp : genital pore - hp : adhesive papillae - ivs : intra capsular seminal vesicle - lm : longitudinal muscle - m : mouth - mp : male pore - ov : ovary - p : proboscis - pg : proboscisglands - ph : pharynx - phg : pharyngial glands - r : retractor muscle - rh : rhabdites - rhg : rhabdite glands - rs : seminal receptacle - s : stylet - sta : statocyst - ut : uterus - t : testis - v : vagina - vg : prostate vesicle - vi : vitellary - vs : seminal vesicle     

The helminth parasites of the lesser flamingo,Phoeniconaias minor (Geoffroy), from Lake Nakuru,Kenya, including a new cestode,Phoenicolepis nakurensis n.g., n.sp.

Summary Seven species of cestodes and two of nematodes are reported from Phoeniconaias minor from Lake Nakuru, Kenya. Phoenicolepis nakurensis n.g., n.sp. (Hymenolepididae) is characterized by the size and shape of the hooks, scolex and strobila, structure of the terminal genital ducts, presence of an accessory sac, external seminal vesicle and stylet, and absence of an internal seminal vesicle. Gynandrotaenia stammeri. Cladogynia phoeniconaiadis, Flamingolepis tengizi, F. dolguschini and Striatofilaria phoenicopteri are redescribed; all except C. phoeniconaiadis are new for this host and for Kenya. ac]19800210Abbreviations as accessory sac - c cirrus - cs cirrus sac - esv external seminal vesicle - g gland cells - gs glandular sheath - isv internal seminal vesicle - md muscular duct - Mg Mehlis' gland - o ovary - pg prostate gland cells - s stylet - sr seminal receptacle - u uterus - v vagina - vd vas deferens - vg vitelline gland     

A new allocreadiid (Trematoda) species from freshwater fish Heterandria bimaculata (Teleostei: Poeciliidae) in Southeastern Mexico

Paracreptotrema heterandriae n. sp. (Trematoda: Allocreadiidae) is described from the intestine of the freshwater fish Heterandria bimaculata (Teleostei: Poeciliidae) from the upper basin of Río La Antigua, in Veracruz, Mexico. The new species is distinguished from the 3 others in the Paracreptotrema Choudhury, Pérez-Ponce de León, Brooks, and Daverdin, 2006 , mainly by having a feeble membranous cirrus sac containing an uncoiled seminal vesicle, instead of a well-developed muscular cirrus sac that encloses coiled seminal vesicle, pars prostatica, and ejaculatory duct as in the previously 3 nominal species. Moreover, eggs of the new species are larger than all others ([measurements in micrometers] eggs of P. heterandriae n. sp. 72.5 [70-75] × 40 [35-41]; P. blancoi 55.4 [52.5-62.5] × 38.5 [32.5-42.5]; P. mendezi 46 × 37; P. profundulusi 57 [52-60] × 27.8 [25-30]).     

Structure of the accessory reproductive glands of the male migratory grasshopper,Melanoplus sanguinipes

The accessory reproductive glands of Melanoplus sanguinipes comprise two bilateral masses of 16 tubules each, distinguishable in sexually mature insects as four white, ten short hyaline, one long hyaline, and a seminal vesicle. Over most of its length, the wall of each tubule consists of a simple glandular epithelium resting on a basal lamina, surrounded by a thin layer of circular muscle. However, near the junction with the ejaculatory duct, the wall of each tubule has a much thickened circular muscle layer and squamous or cuboidal epithelium, the region serving to regulate movement of secretion into the ejaculatory duct. Interdigitation of adjacent epithelial cells is common, and several kinds of specialized junctions occur. In the glandular region, all epithelial cells appear the same and may be flattened, cuboidal, or columnar depending on the tubule type. Except for those of the seminal vesicle, the glandular epithelial cells share ultrastructural features typical of cells engaged in the synthesis of protein for export. Despite these general similarities, in most instances subtle differences occur in the cellular ultrastructure of the epithelia of each tubule and in the appearance of their luminal secretions, suggesting that the tubules are functionally specialized.     

Ultrastructure of copulatory organs in Turbellaria

Summary The copulatory organs in Macrostomum sp. and Microstomum sp. contain simple tubular stylets which are intracellular specializations. The stylet in Macrostomum sp. is produced in a syncytium covering part of the prostatic vesicle. The proximal region of the stylet surrounds the vesicle which contains six prostatic gland ducts and six accessory (sensory) cells containing ciliary rootlets. The stylet in Microstomum sp. is produced in an extension of a syncytium which lines the combined seminal-prostatic vesicle. The stylet is connected to the combined vesicle by a narrow bridge of matrix syncytium through which sperm, prostatic gland products and sensory cilia pass from the vesicle to the stylet lumen. In both species the matrix syncytium can be interpreted as a specialized terminal end of the male canal epithelium. Stylets of Turbellaria and other lower Metazoa are discussed in regards to structure (one or several pieces) and location (in separate cells, in a syncytium, or extracellular).Abbreviations used in figures ac accessory cell - b basal body - c cilium - cv combined vesicle - d prostatic gland duct - dc degenerative cell - di dictyosome - e epidermis - ed ejaculatory duct - g prostatic gland cell - h hemidesmosome - i intercellular matrix - im internal muscle - in intestine; - l lumen of male canal - lm longitudinal muscle - m matrix syncytium - mc male canal epithelial cell - mi microfilaments - mt microtubules - mu muscle cell - mv microvilli - n nucleus - np nerve process - ns neurosecretory (?) granule - p prostatic vesicle - pv prostatic part of combined vesicle - r rootlet - s stylet - sm stylet material - sp sperm - sv seminal part of combined vesicle     

Comparative morphology, homologies, and functions of the male system in oribatid mites (Arachnida: Acari)

The penis is basically a double-walled oval cone. The weak type penis (only 2 species) has a weak tongue, lacks a bridge, and is elongate. The strong type (all others) has a bridge, a strong tongue, thicker walls, and is short. An accessory gland and a common vas deferens always open into the inner cup lumen (= ejaculatory duct). The massive tongue muscles may open the penal orifice. A pair of penal retractor muscles originate on the body wall. Penal protrusion and perhaps partial extrusion of stalk substance is by hemolymph pressure. The penis is completely homologous to the ovipositor. The genital discs are cuticular cups containing glandular tissue and are retractible by muscles originating on the body wall. The minute, rod-like, immobile sperm are mixed with seminal fluid and stalk material secreted by seminal vesicle cells. This mixture is carried via the vase deferentia by peristalsis to the penis. Semen and stalk substance (protein) are somehow separated in the ejaculatory duct into separate pools, with stalk substance nearest the penal orifice. Upon penal protrusion, a bit of stalk material is extruded and fastened to the ground, and upon raising of the mite's body the stalk is “drawn out.” Finally, the ball of semen, adhering to the stalk tip, is pulled through the penal orifice.     

Histological,histochemical, and ultrastructural investigation of the male copulatory apparatus of Haminoea navicula (Gastropoda,Cephalaspidea)

Due to its biological and systematic importance, the morphology and function of the male copulatory apparatus of Haminoea navicula, a Cephalaspidea gastropod mollusk, was investigated by light and electron microscopy. These systems are poorly understood in haminoids, but are often used in the taxonomy of the genus. In H. navicula, the male copulatory apparatus comprises the penis within a penial sheath, a seminal duct and the prostate with two lobes. The penis is a muscular structure with a tip covered by spikes formed by muscular cells. The penial sheath consists of muscular tissue folds lined by an epithelium. Below this epithelium, polysaccharide‐secreting cells and pigment cells were observed. A large number of vacuolar cells were found below the ciliated epithelium of the seminal duct. The proximal lobe of the prostate was formed by tubules that could be divided in basal, middle and apical zones, containing cells that secrete polysaccharides and proteins. The tubules of the prostate distal lobe contained a single type of secretory cells with vesicles that were stained by histochemical techniques for detection of polysaccharides and proteins. Ciliated cells were present along the tubules in both lobes of the prostate. This study revealed a complex prostate with five types of secretory cells, which secrete substances that should be involved in the maintenance and eventually also in the maturation of spermatozoa. A comparison with previous publications, shows that the male copulatory apparatus can differ substantially among cephalaspideans, even between H. navicula and non‐European species attributed to this genus.     

Ultrastructure of the male reproductive organs in the interstitial annelid Sphaerosyllis hermaphrodita (”Polychaeta”, Syllidae)

 The reproductive organs of the simultaneous hermaphrodite Sphaerosyllis hermaphrodita (Syllidae, Exogoninae) were examined by TEM and reconstructed from ultrathin serial sections. Oocytes are produced in the 11–13th chaetigerous segments and then attached to the outer body surface. The male organs comprise a seminal vesicle, testes, sperm ducts and copulatory chaetae. The unpaired seminal vesicle is an uncompartmented cavity above the gut and within the chaetigerous segments 8–10. Its interior is lined with a layer of gland cells that degenerate as spermatogenesis in the vesicle proceeds. The testes are situated ventrolaterally, close to the seminal vesicle in the 9th chaetigerous segment. They contain cells at early stages of spermatogenesis, which are connected to one another by zonulae collares. The testes and seminal vesicle are enclosed in epithelia. Paired sperm ducts run ventrally from about the midline of the body under the seminal vesicle and into the parapodia of the 9th chaetigerous segment. There they open, together with the protonephridia of this segment, to the outside next to the stout copulatory chaeta. Each sperm duct consists of six cells, the luminal surface of which bears microvilli but no cilia. Only in animals with fully differentiated sperm does the small opening of the proximal duct cell in each duct give access to the seminal vesicle. The mode of sperm transfer is discussed. Accepted: 9 December 1996     

Redescription of Synthesium pontoporiae n. comb. with notes on S. tursionis and S. seymouri n. comb. (Digenea: Brachycladiidae Odhner, 1905)

Synthesium pontoporiae n. comb. is redescribed, together with Synthesium tursionis and Synthesium seymouri n. comb.; the parasites were obtained from stranded and accidentally caught cetaceans. The sucker ratio (ratio between widths of the oral and ventral suckers) in S. pontoporiae was 1:1.8-3.0 (mean 1:2.2); in S. tursionis was 1:0.8-1.2; and in S. seymouri was 1:0.5-0.7. Synthesium pontoporiae differed from its congeners by additional diagnostic characters, including: oval to lobed testes; small cirrus with pyriform proximal region and flexible, tubular distal region formed by evagination of ejaculatory duct; and vitellarium in small follicles extending from the level of the seminal vesicle to the posterior extremity of the body and not forming dendritic radial bunches. Data on the morphology of adult S. pontoporiae and S. tursionis were inferred from confocal laser microscopical observations.     

中华绒螯蟹(Eriocheir sinensis)雄性生殖系统的组织学研究

中华绒螯蟹雄性生殖系统的组织学研究表明:生精小管一侧为管壁上皮,另一侧为生发区,生殖细胞由生发区基底部同管腔增殖。输精管分为输精细管和贮精囊,管壁上皮具分泌功能,贮精囊有肌肉层。射精管壁肌肉层较厚,粘膜形成纵行皱襞。副性腺内壁为单层立方上皮。生殖系统发育有明显的季节性,8月开始发育加速,10月进入高峰,4月开始发育停滞。     

The study of the ultrastructure of the female reproductive system in a parasite of bats Allassogonoporus amphoraeformis (Digenea: Allassogonoporidae)

The morphology and fine structure of the female reproductive system of allassogonoporid trematode Allassogonoporus amphoraeformis have been described for the first time. The ovary consists of the germ cells being at various developmental stages and supporting cells of two types. The oviduct, seminal receptacle with its short duct and the proximal portion of Laurer's canal are lined by flattened cellular epithelium with lamellae and cilia on its luminal surface and well-developed basal infoldings. The distal part of Laurer's canal and metraterm are tegumental in structure and are characterized by sparse secretory inclusions and lacking of spines. Mehlis' glands of two types open into ootype. The uterus wall is composed of highly flattened epithelial cells surrounded by basal lamina and sparse muscle bundles. Vitelline lobules consist only of the vitelline cells at various developmental stages. The mature vitelline cells contain two types of inclusions: vitelline droplets and rarely scattered lipids. Vitelline ducts are lined by cellular epithelium with highly folded luminal surface and devoid of cilia. Presented results are compared with earlier obtained data on other lecithodendrioiden trematode Prosthodendrium ascidia ([symbol: see text], 1990).     

Structural and ultrastructural studies of male reproductive tract and spermatozoa in Xylocopa frontalis (Hymenoptera,Apidae)

Fiorillo, B. S., Zama, U., Lino‐Neto, J. and Báo, S. N. 2010. Structural and ultrastructural studies of male reproductive tract and spermatozoa in Xylocopa frontalis (Hymenoptera, Apidae). —Acta Zoologica (Stockholm) 91 : 176–183. In Xylocopa frontalis the reproductive tract is composed of testes, deferent ducts, seminal vesicles, accessory glands and an ejaculatory duct. Each testis comprises four testicular tubules in which multiple cysts are present containing approximately 64 spermatozoa per cyst. The seminal vesicle consists of an epithelium, a thick basement lamina and a muscular external sheet. In the luminal region some vesicles can be observed; however, the epithelial cells of the seminal vesicle do not display morphological features associated with secretory functions. The spermatozoa, measuring approximately 260 µm long, are similar to the hymenopteran pattern. The head region consists of an acrosome with an inner perforatorium that penetrates an asymmetrical nuclear tip. The nucleus is linear, electron‐dense and its posterior tip projects into the beginning of the axoneme. The centriolar adjunct is asymmetric with many electron‐lucent lacunae interspersed throughout. The axoneme has the 9 + 9 + 2 pattern of microtubules and in the posterior region the central microtubules finish first, followed by the doublets and finally the accessory microtubules. The mitochondrial derivatives are asymmetric in both length and diameter with paracrystalline material present only in the larger one. These features may be useful characters for taxonomy and phylogenetic studies.