Distal Centriole Research Articles

Sperm morphology in the black coral Cirrhipathes sp. (Anthozoa, Antipatharia)

Abstract. Male polyps of the antipatharian Cirrhipathes sp., collected along the coral reef of Siladen Island (Sulawesi, Indonesia), were studied in order to gain an insight into the reproductive biology. Spermatocysts (maximum size 120 μm) are located within the primary gametogenic mesenteries and are separated by mesenteric cell cytoplasmic extensions. Sperm, maturing along radial rows, have a fairly round shape and contain a series of electron‐dense vesicles in the apical nuclear region. A single mitochondrion flanks the nucleus. A peculiar cup‐like electron‐dense body, edged with regularly spaced electron‐dense granules, is interposed between the nucleus and the tail, and delimits a central region that includes two centrioles. Cross‐sections of the cup‐like body reveal that the distal centriole has a pericentriolar system, consisting of nine arms arranged in a radial pattern. Each arm branches into three processes that are connected to the electron‐dense granules. Indirect evidence of spawning is derived from the accumulation of sperm in the gastric cavity. This process takes place through the lysis of the cells bordering the mesenteries. Intact cells of this bordering layer appear to be involved in the phagocytosis of non‐expelled gametes.

Preparation and ultrastructure of spermatozoa from Green Poison Frogs, Dendrobates auratus, following hormonal induced spermiation (Amphibia, Anura, Dendrobatidae)

Few ultrastructural studies have been performed on members of the Dendrobatidae, although such investigations can be useful for the understanding of reproductive patterns, as a diagnostic method for males in breeding programs for endangered amphibians and for phylogenetic analysis. The sperm ultrastructure of the Green Poison Frog, Dendrobates auratus, from Panama is described following induced spermiation in living animals. To date only testicular spermatozoa in other dendrobatid frogs have been analysed. Moreover, an electron microscopic preparation method (transmission and scanning electron microscopy) for dendrobatid sperm cells in low concentration is presented. Sperm cells from stimulated frogs (100 IU human chorionic gonadotropin, hCG, twice at an interval of 1 h) were recovered via cloaca lavage using 600 μl isotonic phosphate-free amphibian saline (IPS). Centrifuged flushings (5 min, 173 × g) were deposited on microscopic slides. Adherent spermatozoa were treated with Karnovsky fixative (overnight, 4 °C). After postfixation (2 h, 1% osmium tetroxide), samples were dehydrated in series of ascending acetones (30–100%). For transmission electron microscopy sperm cells were encapsulated using Epon and 1.5% 2,4,6-tris(dimethylaminomethyl)phenol (DMP 30). Ultrathin sections (70 nm) were cut and stained with uranyl acetate (30 min) and lead citrate (5 min). Sperm cells are filiform with a 21.1 ± 2.7 μm long and arcuated head and a single tail (35.0 ± 4.2 μm length). Their acrosomal complex is located at the anterior portion of the head and consists of the acrosomal vesicle which has low electron density, and the subjacent electron-dense subacrosomal cone. In transverse section, the nucleus is circular (1.9 ± 0.2 μm diameter) and conical in longitudinal section. It is surrounded by several groups of mitochondria. The chromatin is highly condensed and electron-dense but shows numerous electron-lucent inclusions. A short midpiece has a mitochondrial collar with a proximal and a distal centriole. The latter gives rise to the axoneme which alone forms the flagellum. The sperm ultrastructure of D. auratus differs from that of other Dendrobatidae because of the absence of a nuclear space and the absence of the undulating membrane associated with an axial fibre. This tail conformation is found in the Ranoidea but not in the Bufonoidea. These results show that the spermatozoa of D. auratus are the first within the Dendrobatidae without accessory tail structures. Methods of using sperm samples from hormonal treated frogs for ultrastructural studies is not only reasonable to examine e.g. amphibian phylogeny without killing frogs threatened with extinction but allows investigations in the field of assisted reproduction and male fertility for example in conservation programs for endangered amphibians.

Sperm ultra-structure of <i>Odontosyllis ctenostoma</i> (Polychaeta: Syllidae) with inferences on syllid phylogeny and reproductive biology

The analysis of the complex reproductive patterns of Syllidae may drastically change the taxonomic hierarchy of the family. To further contribute to the knowledge of Syllidae we have described the sperm ultra-structure and some steps of spermiogenesis of Odontosyllis ctenostoma Claparede, 1868, the first non interstitial eusylline investigated. The mature sperm has a bell-shaped acrosome and contains electron-dense granular material and thin filaments. The barrel-shaped nucleus bears two depressions: one anterior facing the acrosome and the other posterior partially containing the distal centriole and up to six mitochondria. Odontosyllis ctenostoma spermatozoa can be ascribed to the ect-aquasperm type typical of species practising external fertilisation. This morphology is not in complete accordance either with the particular brood protection reported for the species or the egg size. The sperm is similar to those of the Syllinae species thus far investigated, but the acrosome resembles that of the exogonine spermatid. Some authors consider Odontosyllis to be phylogenetically closer to Syllinae, though it shares epigamy with Exogoninae. Others have hypothesised that the exogonine sperm could have been derived from sylline sperm by simplification. In our hypothesis this could have happened through a gradual passage from an Odontosyllis-like eusylline ancestor.

Ultrastructure of spermatozoa of lizards in the genusMabuyafrom Central Brazil

This is the first description of spermatozoal ultrastructure of Mabuya skinks. The spermatozoa of the species studied are filiform, consisting of a head region, a midpiece and a tail. The head is characterized by the following features: a depressed acrosome anteriorly, an acrosome vesicle divided into cortex and medulla, paracrystalline subacrosomal material, a pointed tip perforatorium, a circular perforatorium base plate inside the subacrosomal cone, an epinuclear lucent zone separated from the subacrosomal cone by a membrane, a large nuclear rostrum, and round nuclear shoulders. The midpiece presents a bilateral stratified laminar structure, a distal centriole, peripheral fibres 3 and 8 grossly enlarged, columnar mitochondria with linear cristae, dense body rings and a triangular annulus. Finally, the tail is composed of a principal piece and an end piece. An axoneme and a fibrous sheath characterize the principal piece, and the end piece is formed only by an axoneme, which loses its pattern in the last portion. Comparisons with members of Teiidae revealed differences in the numbers of dense rings. A well-developed epinuclear lucent zone in Mabuya is less prominent among teiids. In the spermatozoa of Mabuya, the first ring of dense bodies is very large, uniquely resembling the condition present in snakes.

Sperm ultrastructure in the inseminating Macropsobrycon uruguayanae (Teleostei: Characidae: Cheirodontinae)

Macropsobrycon uruguayanae is a small, inseminating characid (tetra) of the tribe Compsurini. Although spermatozoa can be found within the ovarian cavity close to oocytes, the exact moment of fertilization has not yet been determined. Spermatozoa have moderately elongate nuclei with electron-dense chromatin. During spermiogenesis, nuclear rotation takes place. Elongate mitochondria with lamellar cristae are found posterior to the nucleus. Centrioles are parallel to one another with the proximal centriole slightly anterior to the longer distal one. The anterior tip of the proximal centriole is located within a shallow nuclear fossa. Electron-dense spurs are associated within the anterior and posterior ends of the distal centriole. Striated centriolar rootlets radiate both anteriorly and posteriorly from the distal centriole. Nine longitudinal accessory microtubules surround the axoneme in the proximal flagellum. The flagellum has a typical 9 + 2 axoneme with no intratubular differentiation. Atypical spermatozoa are also found in the testicular lumen. These cells resemble spermatozoa in most aspects, except that their nuclei are variable in shape, with the granular chromatin less electron-dense than that seen in spermatozoa. The origin and function of these cells could not be determined. The specializations seen in the spermatozoa are discussed as possible adaptations related to the habit of insemination.

Fine structure and morphology of sterlet ( Acipenser ruthenus L. 1758) spermatozoa and acrosin localization

Ultrastructure of sterlet Acipenser ruthenus L. 1758 sperm was examined by scanning and transmission electron microscopy, which allowed us to use various methods for visualizations of different parts of sterlet spermatozoa. Sperm cells possess a head with a distinct acrosome, a midpiece and a single flagellum surrounded by the flagellar plasma membrane. The average length of the head including the acrosome and the midpiece was estimated as 5.14 ± 0.42 μm. Nine to 10 posterolateral projections were derived from the acrosome. Three inter-twining endonuclear canals bounded by membranes traversed the nucleus in its whole length from the acrosome to the implantation fossa. Acrosin was located in all the three parts (acrosome, endonuclear canals and implantation fossa). The proximal and distal centrioles located in the midpiece compacted of nine peripheral triplets of microtubules. One cut of the midpiece contained from two to six mitochondria with area of 215 ± 85 nm 2 in average. The flagellum was 42.47 ± 1.89 μm in length with typical eukaryotic organization of one central pair and nine peripheral pairs of microtubules. It passed through a cytoplasmic channel in the midpiece, which was formed by an invagination at the plasmalemma. The flagellum gradually developed two lateral extensions of its plasma membrane, so-called “fins”. Detected morphological variation can be described by four principal component axes corresponding to groups of individual morphometric characters defined on the sperm structures. Correlations among the characters indicate that the sperms are variable in their shape rather than size. Significant variation among examined fish individuals was found only in flagellum and nucleus length. Comparison between the present and previous studies of morphology of sturgeon spermatozoa confirmed large inter- and/or intra-specific differences that could be of substantial taxonomic value.

Spermatozoon ultrastructure in seven South American species of Tegula Lesson, 1835 (Mollusca: Vetigastropoda) and the phylogenetic implications for the subfamily Tegulinae

Summary This study presents results of the examination of the ultrastructure of the spermatozoon of seven South American species of Tegula using light and transmission electron microscopy. In all cases the spermatozoa were of the primitive or ect-aquaspermatozoon type, common in species which employ external fertilization as part of their reproductive strategy. The spermatozoon of Tegula, from anterior to posterior, are composed of: (a) a bullet-shaped head with an anterior acrosome and a basal nucleus, (b) a mid-piece with a prevalent number of five mitochondria plus proximal and distal centrioles, and (c) a flagellum with a 9+2 arrangement of microtubules. The ultrastructural dimensions of the spermatozoa and the characteristics of the acrosome and the nucleus of the Tegula species studied here, as well as those previously published in the literature, showed that each species produces male gametes having a species-specific morphology. The results also suggest that the ultr structure of the spermatozoon could be potentially useful for recognizing subgenera within Tegula. The comparative study showed that some characters of the spermatozoon of the Tegulinae (e.g. length of the head, acrosome shape, acrosome length as percentage of total head length) agree with fossil, morphological and molecular evidence which suggest that members of this subfamily are more closely related to representative of the family Turbinidae.

Changes of sperm morphology, volume, density and motility and seminal plasma composition inBarbus barbus(Teleostei: Cyprinidae) during the reproductive season

Eighteen spermiating males were randomly selected from a hatchery-reared stock and electronically tagged to record changes in their sperm quality parameters (spermatozoa morphology, ultrastructure and motility, ionic composition and osmolality of the seminal plasma, and sperm volume and density) during the spawning season. Stripping was performed at the beginning of March, April and May. The Barbus barbus spermatozoon has a head without acrosome, a midpiece with 4–6 mitochondria and proximal and distal centrioles, and a flagellum with the typical 9+2 pairs of microtubules. Apart from posterior width of the midpiece, morphological and ultrastructural parameters changed significantly during the reproductive season; generally by decreasing toward the end of reproductive season. Sperm volume also decreased from 0.42 in March to 0.15 ml in May, and density from 18.81 in March to 12.45 × 109 spz ml−1 in May. Osmolality (mOsmol kg−1) was 268 ± 4, 276 ± 2 and 268 ± 2 in March, April and May respectively. Chloride, sodium, calcium and potassium ion concentrations (mM) did not show significant differences between March and April (Cl−: 125.3 vs. 120.5, Na+: 75.7 vs. 69.7, Ca2+: 0.4 vs. 0.3 and K+: 84.7 vs. 84.0). The percentage of motile spermatozoa at 15 s post activation did not show a significant difference between dates, but the highest spermatozoa velocity at 15 s post activation was observed in April (91.4 ± 3.2 µm s−1) and then decreased significantly towards the end of the reproductive season (80.6 µm s−1 in May). However, lowest spermatozoa velocity was measured in March (70.4 ± 1.9 µm s−1). This study supports the hypothesis that longer spermatozoa swim faster. Within one stripping, velocity and percentage motility decreased significantly with time post activation. In conclusion, changes observed in B. barbus sperm parameters during the reproductive season, suggest there is association between such changes and spermatozoa aging processes.

Ultrastructure of Spermatozoa of the Light Bullhead Leiocassis nitidus (Teleostei, Siluriformes, Bagridae)

The spermatozoa of Leiocassis nitidus are relatively simple cells composed of a spherical head, a short midpiece, and a tail, as in most Siluriformes. The ultrastructure is characterized by the following features: Acrosome absent, as in most teleosts; around nucleus about long, with a deep nuclear fossa containing the proximal and distal centrioles and mitochondria. Two centrioles approximately from each other; 10 or more mitochondria surrounding the axoneme (with a 9+2 microtubular pattern), arranged in two layers in the postnuclear cytoplasm and separated from the axoneme by the cytoplasmic canal. Two lateral fins on the same plane as the two central microtubules; doublets 3 and 8, which are ultrastructural characteristics of the sperma tail unlike other siluroids laking the lateral fins.

Comparison of spermiogenesis in the externally fertilizing Hemigrammus erythrozonus and the inseminating Corynopoma riisei (Teleostei: Characiformes: Characidae)

Spermiogenesis and sperm ultrastructure were analyzed in two species of characids with different modes of fertilization: externally fertilizing Hemigrammus erythrozonus and inseminating Corynopoma riisei. Spermiogenesis in H. erythrozonus is characterized by lateral development of the flagellum, nuclear rotation, formation of a shallow nuclear fossa, condensation of the chromatin by elimination of the electron-lucent area from the peripheral region of the nucleus, and renewal of the nuclear membrane. Multilammelated membrane and multivesicular bodies were also observed during elimination of the excess cytoplasm. The spermatozoon exhibits characters typical of "aquasperm," i.e. a spherical head containing a spherical nucleus with highly condensed chromatin, several small mitochondria located at the base of the nucleus within a cytoplasmic collar that extends into a long cytoplasmic sleeve surrounding the anterior part of the single flagellum, which is contained within a cytoplasmic canal. The flagellum lacks fins. The proximal and distal centrioles are nearly parallel to one another, with the anterior tips of both located within shallow nuclear fossae. Spermiogenesis in C. riisei is characterized by nuclear elongation alongside the forming flagellum, formation of an elongate cytoplasmic canal, displacement and elongation of the mitochondria, and uniform condensation of chromatin throughout the nucleus through enlargement of the diameter of the chromatin granules. The spermatozoon has an elongate nucleus with two elongate mitochondria localized to one side. Mitochondria are also located posterior to the nucleus forming a mitochondrial region. The single flagellum, which lacks fins, is lateral to the nucleus and initially contained within the greatly elongate cytoplasmic canal before exiting the canal at its posterior terminus. The spermatozoon of C. riisei exhibits several characters typical of "introsperm," such as an elongate nucleus and midpiece (mitochondrial region). The nuclear chromatin in the spermatozoon remains "flocculent" and is never as condensed as that seen in many characid sperm. Differences in spermiogenesis between externally fertilizing and inseminating characids are discussed.

Spermatid Differentiation and Sperm Ultrastructure of the Granular Ark, Tegillarca granosa (Bivalvia: Arcidae)

This study describes spermatogenesis and sperm ultrastructure of the granular ark, Tegillarca granosa using light and electron microscopy. In the active spermatogenic season, the testis comprises many spermatogenic follicles that contain germ cells in different developmental stages. Primary spermatocytes in the pachytene stage are characterized by synaptonemal complexes. The early spermatids are characterized by the appearance of several Golgi bodies, increased karyoplasmic electron density, and tubular mitochondria. The mass of proacrosomal granules consists of numerous heterogeneous granules with high electron density that are about 20 nm in diameter. From the midstage of spermiogenesis, the well-developed mitochondria in the cytoplasm aggregate posterior to the nucleus and surround the proximal and distal centrioles. The proacrosomal granules condense and form a single acrosome with a thin envelope. During late spermiogenesis, the acrosome begins to elongate becoming conical. The sperm is approximately <TEX>$35.0{\mu}m$</TEX> long and consists of a head, midpiece, and tail. The head comprises a round nucleus and a conical acrosome. A micro fibrous axial rod is observed between the nucleus and acrosome. The midpiece has a calyx-like structure with five mitochondria, and the tail, which has the typical "9+2" microtubular system, originates from the distal centriole.

Spermiogenesis in Soft‐Shelled Turtle, Pelodiscus sinensis

Spermiogenesis in the soft-shelled turtle, Pelodiscus sinensis, was examined by transmission electron microscopy. The process includes nuclear elongation, chromatin condensation, acrosomal and flagellar development, and elimination of excess cytoplasm. In stage I, the proacrosomal vesicle occurs next to a shallow fossa of the nucleus, and a dense acrosomal granule forms beneath it. A smaller subacrosomal granule in the middle of the fibrous layer is related to the development of intranuclear tubules. The nucleus begins to move eccentrically. In stage II, the round proacrosomal vesicle is flattened by protrusion of the nuclear fossa, and the dense acrosomal granule diffuses into the vesicle, as the fibrous layer forms the subacrosomal cone. Circular manchettes develop around the nucleus, and the chromatin coagulates into small granules. The movement of the nucleus causes rearrangement of the cytoplasm. In stage III, the front of the elongating nucleus protrudes out of the spermatid and is covered by the flat acrosome; coarse granules replace the small ones within the nucleus. At the posterior pole of the head, mitochondria move backward. Numerous microtubules begin to assemble the axoneme of flagellum. In stage IV, the chromatin concentrates to dense homogeneous phase. The circular manchette is reorganized longitudinally. The Sertoli process covers the acrosome and the residues of the cytoplasmic lobes are eliminated. In stage V, the sperm head matures. After dissolution of the longitudinal manchette, the mitochondria arrange themselves around the proximal and distal centrioles. Caudal to the mitochondrial mass, a fibrous sheath surrounds the proximal portion of the flagellum.

모래무지(Teleostei, Cyprinidae) 정자변형과정과 정자의 미세구조

Spermiogenesis and mature spermatozoa of the Korean false minnow Pseudogobio esocinus (Cyprinidae) are described by means of scanning and transmission electron microscopy. Spermiogenesis is characterized by lateral development of the flagellum, absence of nuclear rotation, and eccentric nuclear fossa formation. The spermatozoa have a spherical head containing a nucleus with highly condensed chromatin and no acrosome. The nuclear fossa contains the proximal centriole and anterior part of the distal centriole. The midpiece is type A II and contains semi-fused mitochondria around the axoneme. However, the symmetrical distribution of 4 or more the mitochondria does not follow a general pattern of the cyprinid spermatozoa. Cytoplasmic vesicles in the midpiece are common in Cypriniformes and some of Siluriformes and Characiformes spermatozoa.

Fine structure of spermatozoa in the gilthead sea bream (Sparus aurata Linnaeus, 1758) (Perciformes, Sparidae).

Scanning and transmission electron microscopy were used to investigate the fine structure of the sperm of the sparid fish Sparus aurata L. The mature spermatozoon of gilthead sea bream belongs, like that of the other sparid fish, to a "type I" as defined by Mattei (1970). It has a spherical head which lacks an acrosome, a short, irregularly-shaped midpiece and a long cylindrical tail. The nucleus reveals a deep invagination (nuclear fossa) in which the centriolar complex is located. The two centrioles are approximately perpendicular to each other and show a conventional "9+0" pattern. The proximal centriole is associated with a cross-striated cylindrical body lying inside a peculiar satellite nuclear notch which appears as a narrow invagination of the nuclear fossa. The distal centriole is attached to the nuclear envelope by means of a lateral plate and radial fibres made of an electron-dense material. The short midpiece houses one mitochondrion. The flagellum is inserted perpendicularly into the base of the nucleus and contains the conventional 9+2 axoneme.

Ultrastructural observations on spermiogenesis in the peanut worm, Themiste pyroides (Chamberlin, 1920) (Sipuncula; Sipunculidea)

Summary The process of spermiogenesis and the ultrastructure of the spermatozoa in the peanut worm, Themiste pyroides, from the Sea of Japan were observed with electron microscopy (SEM and TEM). The testes are composed of groups of spermatogonia and are covered by peritoneal cells. Clusters of spermatocytes are released from the testes into the coelomic fluid. Connected by intercellular bridges, the spermatocytes within a given cluster develop asynchronously. Proacrosomal vesicles and a flagellum appear in spermatocytes. Spermatids in the clusters retain the intercellular connections. During spermiogenesis, the acrosomal vesicle, formed by coalescence of small proacrosomal vesicles in the basal part of the spermatid, migrates to the apical part of the cell to form a conical-shaped acrosome. The basal concavity lying above the nucleus is filled with subacrosomal substance. The midpiece contains four mitochondria, two centrioles, and some residual cytoplasm with dark glycogen-like granules. A peculiar annulus structure develops around the base of the flagellum. The distal centriole has a pericentriolar complex consisting of radially oriented elements. Before the spawning process, the spermatozoa are filtered throughout the ciliary nephrostomal funnel into the excretory sac of paired nephridia where they are stored for a short time. The sperm are released into the sea water via nephridiopores. Spermatozoa remaining in the coelomic fluid after spawning are resorbed by amoebocytes. This species from Vostok Bay is characterized by a prolonged spawning period from June to early October. The reproductive strategy of T. pyroides is discussed in comparison with that of Thysanocardia nigra, the latter having a unique pattern of packaging of the spermatozoa, resulting in the formation of spermatozeugmata, as a reproductive adaptation to the very short spawning period.

Sperm ultra-structure and spermiogenesis in &lt;i&gt;Syllis krohni&lt;/i&gt; (Polychaeta: Syllidae), with some observations on its reproductive biology

yllidae show a wide spectrum of both reproductive strategies and sperm types. Analysis of their reproductive patterns could drastically change the presently accepted taxonomic hierarchy of the group. To further contribute to the knowledge of Syllidae we have described the sperm ultra-structure and the spermiogenesis of Syllis krohni (Ehlers, 1864). Mature sperm has a cone-shaped acrosome whose distal end is notched by a trough that transversely encircles its anterior portion. During spermiogenesis, the acrosomal vesicle undergoes modifications leading to its final shape with a posterior opening. The nucleus appears flattened anteriorly and forms a cleft that surrounds the proximal centriole in its distal region. A 9+2 flagellar axoneme is observed. Up to five mitochondria surround the distal centriole. The spermatozoon of S. krohni can be ascribed to the ect-aquasperm type that is typical in species having external fertilisation and appears to be very similar in appearance to that of the congeneric species thus far investigated. The main difference is in the shape of the acrosome, which is more elongated and as long as the nucleus. Reproduction of syllids seems to be conservative within sub-families, and the sperm morphology can probably help in phylogenetic reconstruction. External fertilisation is a widespread strategy within the genus Syllis , probably leading to a substantial similarity in sperm morphology being maintained. It is hypothesised, however, that within the same sperm type linked to a particularly reproductive strategy, the acrosome ultra-structure can be indicative of phylogeny.

Reproductive morphology of Brittanichthys axelrodi (Teleostei: Characidae), a miniature inseminating fish from South America

Light and electron microscopy were used to investigate the morphology of reproductive characters in a characid fish, Brittanichthys axelrodi. Spermatozoa were found in ovaries of females, thereby confirming insemination in this species. Bony hooks can be found on the fourth unbranched ray and branched rays 1-4 of the anal fin and the unique sigmoidally-curved ray of the caudal fin in mature males. Testes have three distinct regions: an anterior spermatogenic region, an aspermatogenic middle region lined with a simple squamous epithelium and used for storage of mature spermatozoa, and a posterior region of coiled chambers lined with a high simple cuboidal epithelium. The most posterior region appears to be instrumental in the formation and storage of spermatozeugmata, unencapsulated sperm packets. Thus far, this tripartite testis morphology is unique among characids. The mature spermatozoon has an elongate nucleus ( approximately 5 microm in length). A striated rootlet originates at the anterior end of the distal centriole and continues to the anterior tip of the cell. The striated rootlet wraps around the entire ventral area of the anterior part of the nucleus and appears to continue around the anterior tip of the nucleus and down the dorsal side as electron-dense material. Several large, spherical mitochondria ( approximately 0.6 microm in diameter) with lamellar cristae overlap the posterior end of the nucleus and continue beyond together with the cytoplasmic collar that contains the flagellum which lacks axonemal fins. Each spermatozeugma is lanceolate in shape when sectioned mid-sagitally, with the core staining positively for mucopolysaccharides. In both sexes, the gonopore opens posterior to the anus, with the urinary pore having a separate opening posterior to the gonopore. Bands of skeletal muscle were found in the area of the male gonopore. These morphological features are likely linked to the reproductive mode of insemination, a trait that is so far as known, relatively rare among teleost fishes, but is proving increasingly frequent among certain groups of characid fishes.

Ultrastructure of the spermatozoon of Myrmecocichla formicivora (Vieillot, 1881) and Philetairus socius (Latham, 1790) (Aves; Passeriformes), with a new interpretation of the passeridan acrosome

AbstractPasserine spermatozoa exhibit apomorphies that distinguish them from non‐passerine neognaths and palaeognaths. The acrosome is longer than the nucleus (excepting the suboscines, most Corvida, and a few Passerida). A perforatorium and endonuclear canals are absent. The proximal centriole is absent (except in the suboscines). The distal centriole is secondarily short, contrasting with its elongate condition in palaeognaths and Galloanserae. In the Passerida a single mitochondrial strand winds extensively along the axoneme (restricted to the anterior axoneme in suboscines and Corvida). A fibrous, or amorphous, periaxonemal sheath, seen in palaeognaths and many non‐passerines, respectively, is absent. The acrosome in Myrmecocichla formicivora and Philetairus socius is bipartite: an acrosome core is surmounted by an acrosome crest; the core is ensheathed by a layer which is a posterior extension of the crest. The acrosome helix is a lateral extension of the crest and the crest layer with (Myrmecocichla) or without (Philetairus) protrusion of material of the acrosome core into it. In M. formicivora, as in other muscicapoids, a fibrous helix is intertwined with at least the more proximal region of the mitochondrial helix. The fibrous helix is absent at maturity in Philetairus and other described passeroid spermatozoa with the possible exception of Passer italiae. In Philetairus a granular helix precedes the mitochondrial helix.

SPERM MORPHOLOGY AND SPERMATOGENESIS IN THE TUBE-WORM POMATOLEIOS KRASSII (POLYCHAETA: SPIROBRANCHINAE) FROM THE SUEZ BAY, EGYPT.

he mature sperm morphology and spermatogenesis ultrastructure have been fully described in Pomatoleios krassii, which is a spirobranchian polychoaete attached to rocks, wrecked boats, rods and hard substrates at some polluted sites on Suez Bay coast. Sperms develop in the coelom as free-floating plasmodial cells. At the end of spermatogenesis, mature sperms float freely in the coelom. The spermatogonia are relatively large in size (13 µ in diameter). The spermatozoon of the present species differs from that of other polychaete species by having a large head (6 µ in length) formed of rounded nucleus and large acrosome which forms a large curved terminal cap on the nucleus. This may be an indication that fertilization occurs by some mechanisms that limit exposure of such fragile gametes to any possiple pollution. Meanwhile, female of P.kraussii protects its eggs with a jelly mass attached to the branchial crown, and the sperm is required to penetrate the matrix of egg mass. The large pair of mitochondria (2 µ in diameter) and presence of two pairs of proximal and distal centrioles which are not recorded so for in previous studies, as well as the long tail may be correlated with a characteristic movement of the sperm to reach female branchial crown, where the egg masses are found.

Ultrastructure of spermatozoa of tench Tinca tinca observed by means of scanning and transmission electron microscopy

Structure of tench ( Tinca tinca L.) spermatozoa was investigated by means of scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Spermatozoa of 26.1 ± 3.8 μm total length possessed typical primitive simple structure, called “aqua sperm”, without acrosomal head structures. It was probably the smallest spermatozoon described among cyprinid fishes. Heads were mostly composed of dense and slightly granular material, which appeared to be fairly homogeneous except for the occasional appearance of vacuoles. The midpiece remained separated from the flagellum by the cytoplasmic channel; it was cylindric/cone-shaped, 0.86 ± 0.27 μm in length and 1.17 ± 0.24 μm in width at proximal part. The proximal centriole was located in the “implantation fossa”. The distal centriole appeared almost tangential to the nucleus and it functioned as a basal body for the flagellum. It had an orientation of 140° with respect to the distal centriole. The sperm flagellum with 25.45 ± 2.47 μm of total length had no any fin. The diameter of the flagellum perpendicular to the plane of the doublet of central microtubules was 173.67 ± 20.45 nm and horizontal plane of the central microtubules was 200.71 ± 20.45 nm. Peripheral doublets and the central doublet of microtubules measured 23.39 ± 3.18 and 35.88 ± 4.44 nm in width, respectively. The diameter of a microtubule was only 9.14 ± 2.97 nm. A vesicle was attached to the most basal region of the flagellum and located just under plasma membrane of the flagellum.