Differences in sperm morphology in foam‐nesting leptodactyline frogs (Anura,Leptodactylidae)

Sperm morphology is diverse among vertebrates and is influenced by the reproductive strategies adopted by species. In anurans, sperm morphology is associated with reproductive modes and mating systems. Here, we describe the sperm morphology of 11 frog species in the genus Leptodactylus and that of Lithodytes lineatus and discuss the relationship between sperm morphology and species' mating systems. We observed two distinct sperm morphotypes among the leptodactyline species, which differed mostly in head morphology. Type I sperm had triangular head, discrete acrosome vesicle with posterior margin not clearly visible; type II sperm had elongated head, clear acrosomal vesicle with posterior margin clearly visible. These sperm types do not seem to be associated with phylogeny; instead, type II sperm was observed in all polyandrous species analysed and in species with evidences of polyandry. Moreover, sperm of all species presented tail with undulating membrane connected to the axial fibre. We suggest that differences in sperm morphology might be associated with sperm competition to what polyandrous species are subjected. However, natural history observations on polyandrous mating in some species presenting type II sperm and phylogenetic comparative studies are need to elucidate the role of mating systems in the evolution of sperm morphology in leptodactylines.     

The fine structure of the sperm of a holothurian and an ophiuroid

The fine structure of the mature sperm of the holothurian, Cucumaria miniata, and the ophiuroid, Ophiopholis aculeata, is described with particular reference to their acrosomal and centriolar satellite complexes, and compared to the sperm of other echinoderms. In Cucumaria, the acrosome is in the form of a diffuse acrosomal vesicle. It is unusual in that it apparently lacks an acrosomal membrane. A membrane separating the acrosomal vesicle from the periacrosomal material may not be equivalent to a typical inner acrosomal membrane. In Ophiopholis, the acrosome is dense, with some internal substructure, and is enclosed by a complete acrosomal membrane. In both species, the acrosome is partially surrounded by an amorphous periacrosomal mass. There is a notable absence of a subacrosomal depression and associated structures as found in other echinoderm sperm. The centriolar satellite complex (CSC) is essentially identical in both species. A reconstruction of the CSC is presented. The CSC consists of nine satellites radiating angularly from the distal centriole, each bifurcating at a dense node before inserting on a marginal ring containing circumferential microtubules. The ring is probably a cytoskeletal element. Immediately below the satellites are nine Y-shaped connectives. connecting each of the axonemal alpha doublets to the flagellar membrane.     

Sperm Bundles in the Seminal Vesicle of the Crematogaster victima (Smith) Adult Males (Hymenoptera: Formicidae)

This study establishes the presence of spermatodesm in the seminal vesicles of sexually mature males of Crematogaster victima (Smith). In this species, the spermatozoa are maintained together by an extracellular matrix in which the acrosomal regions are embedded. This characteristic has not yet been observed in any other Aculeata. However, the sperm morphology in this species is similar to that described for other ants. The spermatozoa measure on average 100 μm in length, and the number of sperm per bundle is up to 256. They are composed of a head formed by the acrosome and nucleus; this is followed by the flagellum, which is formed by the centriolar adjunct, an axoneme with a 9?+?9?+?2 microtubule pattern, two mitochondrial derivatives, and two accessory bodies. The acrosome is formed by the acrosomal vesicle and perforatorium. The nucleus is filled with compact chromatin with many areas of thick and non-compacted filaments. Both mitochondrial derivatives have the same shape and diameters. The presence of sperm bundles in sexually mature males differentiates C. victima from other ants; however, the similarities in the sperm ultrastructure support the monophyly of this insect group.     

ROLE OF THE GAMETE MEMBRANES IN FERTILIZATION IN SACCOGLOSSUS KOWALEVSKII (ENTEROPNEUSTA) : I. The Acrosomal Region and Its Changes in Early Stages of Fertilization

Previous electron microscope studies of sperm-egg association in the annelid Hydroides revealed novel aspects with respect to the acrosomal region. To determine whether these aspects were unique, a comparable study was made of a species belonging to a widely separated phylum, Hemichordata. Osmium tetroxide-fixed polyspermic material of the enteropneust, Saccoglossus, was used. The acrosomal region includes the membrane-bounded acrosome, with its large acrosomal granule and shallow adnuclear invagination, and the periacrosomal material which surrounds the acrosome except at the apex; here, the acrosomal membrane lies very close to the enclosing sperm plasma membrane. After reaching the egg envelope, the spermatozoon is activated and undergoes a series of changes: the apex dehisces and around the resulting orifice the acrosomal and sperm plasma membranes form a continuous mosaic membrane. The acrosomal granule disappears. Within 7 seconds the invagination becomes the acrosomal tubule, spans the egg envelopes, and meets the egg plasma membrane. The rest of the acrosomal vesicle everts. The periacrosomal mass changes profoundly: part becomes a fibrous core (possibly equivalent to a perforatorium); part remains as a peripheral ring. The basic pattern of structure and sperm-egg association in Saccoglossus is the same as in Hydroides. Previous evidence from four other phyla as interpreted here also indicates conformity to this pattern. The major role of the acrosome is apparently to deliver the sperm plasma membrane to the egg plasma membrane.     

Gamete ultrastructure in the arctic holothurian Molpadia borealis M. Sars, 1859 (Holothuroidea: Molpadiidae)

This study examines the gonad condition and gamete morphology of the Arctic deep-sea holothurian Molpadia borealis M. Sars, 1859 (Molpadiidae) collected from the Kara Sea in September 2006. The intensive process of gametogenesis observed in the holothurian gonads was close to completion, suggesting upcoming spawning. The sperm ultrastructure in M. borealis is similar to that in most Holothuroidea. This species has classic flagellated sperm, echinosperm, which are typical of animals with external insemination. The sperm head has a 2.5-??m spherical nucleus with a proximal acrosome consisting of a spherical acrosomal vesicle surrounded by periacrosomal material. A single circular mitochondrion located in the sperm mid-piece surrounds the proximal and distal centrioles, which are arranged at an obtuse angle to each other. The eggs of M. borealis are approximately 300 ??m in diameter. This suggests indirect development with a planktotrophic larva. This type of development of M. borealis is probably related to life in high latitudes in the deep sea.     

Actin-like filaments in the acrosomal apparatus of spermatozoa of a sea urchin

The acrosomal apparatus of a sea urchin, Echinocardium cordatum, consists of an acrosomal vesicle and a post-acrosomal rod. The rod is 2.5 μm long and extends from the acrosomal vesicle to the bottom of a nuclear invagination. The rod consists of a bundle of longitudinally disposed, 60 Å thick, actin-like filaments which bind heavy meromyosin to form arrowhead complexes. The actin-like filaments may have a dual function in the fertilization process: (1) extension of the acrosomal process through the egg investments; (2) incorporation of the sperm nucleus.     

Assembly of the fluorescent acrosomal matrix and its fate in fertilization in the water strider,Aquarius remigis

Animal sperm show remarkable diversity in both morphology and molecular composition. Here we provide the first report of intense intrinsic fluorescence in an animal sperm. The sperm from a semi‐aquatic insect, the water strider, Aquarius remigis, contains an intrinsically fluorescent molecule with properties consistent with those of flavin adenine dinucleotide (FAD), which appears first in the acrosomal vesicle of round spermatids and persists in the acrosome throughout spermiogenesis. Fluorescence recovery after photobleaching reveals that the fluorescent molecule exhibits unrestricted mobility in the acrosomal vesicle of round spermatids but is completely immobile in the acrosome of mature sperm. Fluorescence polarization microscopy shows a net alignment of the fluorescent molecules in the acrosome of the mature sperm but not in the acrosomal vesicle of round spermatids. These results suggest that acrosomal molecules are rearranged in the elongating acrosome and FAD is incorporated into the acrosomal matrix during its formation. Further, we followed the fate of the acrosomal matrix in fertilization utilizing the intrinsic fluorescence. The fluorescent acrosomal matrix was observed inside the fertilized egg and remained structurally intact even after gastrulation started. This observation suggests that FAD is not released from the acrosomal matrix during the fertilization process or early development and supports an idea that FAD is involved in the formation of the acrosomal matrix. The intrinsic fluorescence of the A. remigis acrosome will be a useful marker for following spermatogenesis and fertilization. J. Cell. Physiol. 226: 999–1006, 2011. © 2010 Wiley‐Liss, Inc.     

FINE STRUCTURE OF THE SPERMATOZOON OF HYDROIDES HEXAGONUS (ANNELIDA), WITH SPECIAL REFERENCE TO THE ACROSOMAL REGION

This paper describes in some detail the structure of the acrosomal region of the spermatozoon of Hydroides as a basis for subsequent papers which will deal with the structural changes which this region undergoes during fertilization. The material was osmium-fixed and mild centrifugation was used to aggregate the spermatozoa from collection to final embedding. The studies concern also the acrosomal regions of frozen-thawed sperm prepared by a method which previously had yielded extracts with egg membrane lytic activity. The plasma membrane closely envelops four readily recognizable regions of the spermatozoon: acrosomal, nuclear, mitochondrial, and flagellar. The acrosome consists of an acrosomal vesicle which is bounded by a single continuous membrane, and its periphery is distinguishable into inner, intermediate, and outer zones. The inner and intermediate zones form a pocket into which the narrowed apex of the nucleus intrudes. Granular material adjoins the inner surface of the acrosomal membrane, and this material is characteristically different for each zone. Centrally, the acrosomal vesicle is spanned by an acrosomal granule: its base is at the inner zone and its apex at the outer zone. The apex of the acrosomal granule flares out and touches the acrosomal membrane over a limited area. In this limited area the adjoining granular material of the outer zone is lacking. The acrosomal membrane of the inner zone is invaginated into about fifteen short tubules. The acrosomal membrane of the outer zone is closely surrounded by the plasma membrane. At the apex of the acrosomal region a small apical vesicle is sandwiched between the plasma membrane and the acrosomal membrane. Numerous frozen-thawed specimens and occasional specimens not so treated show acrosomal regions at the apex of which there is a well defined opening or orifice. Around the rim or lip of this orifice plasma and acrosomal membranes may even be fused into a continuum. The evidence indicates that the apical vesicle and the parts of the plasma and acrosomal membranes which surround it constitute a lid, and the rim of this lid constitutes a natural "fracture line" or rim of dehiscence. Should fracture occur, the lid would be removed and the acrosomal vesicle would be open to the exterior.     

Polymerization of actin without acrosomal exocytosis in starfish sperm : Visualization with NBD-phallacidin

Polymerized actin sperm of the starfish Pisaster ochraceus is stained intensely by NBD-phallacidin in the fluorescence microscope. Parallel phase contrast, Nomarski and scanning electron microscopy (SEM) illustrate other changes brought about in sperm treated with the calcium ionophore A23187 and NH₄Cl. A complete acrosome reaction is elicited by A23187, including exocytosis of the acrosomal vesicle and formation of a long acrosomal process which is filled with polymerized actin. Considerable actin polymerization is caused by NH₄Cl, but the acrosomal vesicle is not exocytosed. The various patterns of NH₄Cl-mediated polymerization of sperm actin always include bundles which project backward from the actomere and often others which project quite far forward in front of the acrosomal vesicle. These patterns are discussed in terms of the possible triggers and mechanisms of forming actin bundles in sperm.     

A reevaluation of the fertilizin hypothesis of sperm agglutination and the description of a novel form of sperm adhesion

The classical isoagglutination of sea urchin sperm by egg jelly is not an agglutination of cells, as proposed by the fertilizin-antifertilizin hypothesis. Sperm motility is required to obtain the isoagglutination of Strongylocentrotus purpuratus sperm, and the sperm do not adhere to each other in the isoagglutination clusters, which cannot be fixed for microscopy and which disperse rapidly into individual cells when sperm motility is inhibited. These observations suggest that isoagglutination is the swarming of freely moving sperm to a common focus and is quite distinct from the agglutination of sperm by known crosslinking agents (antibodies or lectins).A previously unrecognized form of sperm agglutination is described which follows induction of an acrosome reaction by egg jelly, ammonia, or the ionophore A23187 in a suspension of sea urchin or sand dollar sperm. The sperm form rosettes of up to 100 cells in which the newly extended acrosomal processes adhere to each other. Rosettes can form containing sperm of different species, in which the acrosomal processes adhere without species preference.As observed by transmission electron microscopy, the acrosomal process of Lytechinus pictus sperm consists of an acrosomal tubule covered by a sheath of extracellular material. Rosette formation results from attachment between the extracellular materials of adjacent sperm.Less frequently, the acrosomal process of one sperm adheres to the midpiece of another by fusion of the acrosomal tubule and midpiece plasma membranes.     

Fine structure of Lasaea subviridis and Mysella tumida sperm (Bivalvia,Galeommatacea)

Summary Lasaea subviridis and Mysella tumida sperm resemble the primitive spermatozoan type, but exhibit several unique morphological features. L. subviridis sperm heads vary in shape and size owing to differing degrees of nuclear condensation. A fully mature, heterogenous acrosomal vesicle with an associated axial rod is present. Up to 50% of L. subviridis sperm in developing gonads have conspicuously angled flagella that propel the sperm cells in irregular helical paths. This may represent a penultimate stage in sperm development because the remainder of the sperm cells have posteriorly-directed flagella and swim in a nonhelical anterior direction. A trend toward a reduction in both nuclear condensation and swimming ability may be a long-term consequence of increasing degrees of localized, but non-internal self-fertilization in marine invertebrates that brood. Mysella tumida sperm are monomorphic and possess numerous microvilli (30–60 nm in diameter and up to 5.7 m in length) that resemble stereocilia and radiate from the cell membrane surrounding the basal body. In this species, the sperm cell does not have an axial rod, and the complex acrosomal vesicle contains five distinct zones of varying electron opacity. One of these zones is a transverse, electron-opaque band that is apparently composed of rolled-up membrane. Following acrosomal breakdown, this membrane unfolds to cover the anterior tip of the sperm cell. Although both L. subviridis and M. tumida are hermaphroditic, the relative size of their male investments is conspicuously different. Approximately 40–50% of the M. tumida gonadal volume is testis compared with about 5% of that in L. subviridis.     

COMPARATIVE SPERM MORPHOLOGY OF THE PULMONATE LIMPETS TRIMUSCULUS COSTATUS, T. RETICULATUS (TRIMUSCULIDAE) AND BURNUPIA STENOCHORIAS AND ANCYLUS FLUVIATILIS (ANCYLIDAE)

Sperm ultrastructure is described for the first time in representativesof the pulmonate ‘limpet’ families Trimusculidae(Trimusculus costatus, T. reticulatus: marine) and Ancylidae(Burnupia stenochorias, Ancylus fluviatilis: freshwater). Allshow characteristic heterobranch sperm features (a spheroidalacrosomal vesicle supported by an acrosomal pedestal; a helicallykeeled nucleus and a complex, very elongate midpiece featuringparacrystalline and matrix layers sheathing the axoneme, coarsefibers and one or more glycogen helices). Posterior to the midpiece,a glycogen piece (axoneme sheathed by glycogen granules) andannulus are also present in all species. Taxonomically usefuldifferences in the shape and dimensions of the acrosome, nucleusand midpiece occur between the species. Results support thedecision of recent workers to transfer the Trimusculidae fromthe Siphonarioidea to a separate superfamily Trimusculoidea(characteristic sperm features including: narrow acrosomal pedestaloverlapping with nuclear apex; heavily keeled nucleus; midpiecewith strongly projecting secondary and glycogen helices). Therelationship of the Trimusculoidea to other pulmonates, as indicatedby sperm ultrastructure, remains uncertain largely because comparativedata for several important groups are unavailable. Spermatozoaof the two ancylids most closely resemble those of other investigatedplanor-boideans and to a lesser extent, those of the Lym-naeoidea.However, differences between Burnupia stenochorias (unique(?)accessory structure on the acrosomal pedestal; glycogen wedgeswithin the nuclear fossa; other features similar to planorbids)and Ancylus fluviatilis (all sperm features very similar toplanorbids) suggests that these patelliform ancylids are notclosely related. (Received 20 November 1997; accepted 23 January 1998)     

CHANGES IN THE SPERMATOZOON DURING FERTILIZATION IN HYDROIDES HEXAGONUS (ANNELIDA) : I. Passage of the Acrosomal Region through the Vitelline Membrane

In the previous paper the structure of the acrosomal region of the spermatozoon was described. The present paper describes the changes which this region undergoes during passage through the vitelline membrane. The material used consisted of moderately polyspermic eggs of Hydroides hexagonus, osmium-fixed usually 9 seconds after insemination. There are essentially four major changes in the acrosome during passage of the sperm head through the vitelline membrane. First, the acrosome breaks open apically by a kind of dehiscence which results in the formation of a well defined orifice. Around the lips of the orifice the edges of the plasma and acrosomal membranes are then found to be fused to form a continuous membranous sheet. Second, the walls of the acrosomal vesicle are completely everted, and this appears to be the means by which the apex of the sperm head is moved through the vitelline membrane. The lip of the orifice comes to lie deeper and deeper within the vitelline membrane. At the same time the lip itself is made up of constantly changing material as first the material of the outer zone and then that of the intermediate zone everts. One is reminded of the lip of an amphibian blastopore, which during gastrulation maintains its morphological identity as a lip but is nevertheless made up of constantly changing cells, with constantly changing outline and even constantly changing position. Third, the large acrosomal granule rapidly disappears. This disappearance is closely correlated with a corresponding disappearance of a part of the principal material of the vitelline membrane from before it, and the suggestion is made that the acrosomal granule is the source of the lysin which dissolves this part of the vitelline membrane. Fourth, in the inner zone the fifteen or so short tubular invaginations of the acrosomal membrane, present in the normal unreacted spermatozoon, lengthen considerably to become a tuft of acrosomal tubules. These tubules are the first structures of the advancing sperm head to touch the plasma membrane of the egg. It is notable that the surface of the acrosomal tubules which once faced into the closed acrosomal cavity becomes the first part of the sperm plasma membrane to meet the plasma membrane of the egg. The acrosomal tubules of Hydroides, which arise simply by lengthening of already existing shorter tubules, are considered to represent the acrosome filaments of other species.     

Ultrastructural investigations of testes and spermiogenesis in two species of halacarid mites (Halacaridae, Actinedida, Actinotrichida): Thalassarachna basteri from the Baltic Sea and Halacarellus thomasi from McMurdo Sound (Antarctica)

Testes and sperm cells of two species of halacarid mites, Thalassarachna basteri from the Baltic Sea and Halacarellus thomasi from McMurdo Sound (Antarctica), were investigated. Testes are paired structures, composed of a glandular and a germinal part. The testicular lumen is filled with a very complex secretion that contributes to sperm cell aggregates. Early spermatids of T. basteri display unusual chromatin condensation within the nucleus, but the formation of an acrosomal complex with a small acrosomal vesicle and a long acrosomal filament can be regarded as typical for the group. Tubular invaginations of the plasmalemma occur at the cell periphery. A deep, ring-like infold divides the cell into one part containing the chromatin body and another containing mainly the invaginations and the acrosomal complex. The mature sperm cell is ovoid, aflagellate and surrounded by a distinct secretion sheath. In H. thomasi only a limited number of spermiogenesis stages were observable. Chromatin condensation was rather similar and peripheral invaginations also occurred. However, no acrosomal complex was observed in the early stages. The division of the mature sperm cells into two halves was even more pronounced in H. thomasi, since one half of the cell contained masses of convoluted structures. The same half also contained a structure that remotely resembled an acrosomal complex. The observed differences between T. basteri and H. thomasi sperms support the placing of the two halacarids in separate genera.     

东方扁虾精子的超微结构

利用电镜研究了东方扁虾（Ｔｈｅｎｕｓ ｏｒｉｅｎｔａｌｉｓ）精子的形态和结构。精子由核、膜复合物区和顶体区３部分组成。核内含非浓缩的染色质、微管及细纤维丝,外被核膜;５～６条辐射臂自核部位伸出,臂内充满微管。膜复合物区位于核与顶体之间,由许多膜片层结构及其衍生的囊泡共同组成。顶体区由顶体囊和围顶体物质组成,顶体结构复杂,由顶体帽、内顶体物质和外顶体物质等构成;围顶体物质呈细颗粒状,主要分布于顶体囊     

THE ACROSOME REACTION IN MYTILUS EDULIS : I. Fine Structure of the Intact Acrosome

The intact acrosome of the Mytilus edulis spermatozoon consists of a conical vesicle, the basal side of which is deeply invaginated so that the whole vesicle forms a sheath around a very slender axial rod, about 2.7 µ long, inserted in a tube passing through the nucleus. The annular base of the acrosomal vesical is filled with a homogeneous substance; the outer wall of the vesicle is lined with a somewhat irregular layer of a particulate substance interspersed with very fine tubular elements, and its lumen is nearly filled by a strand of material which extends from the inner tip of the invagination to the apex of the acrosome. The lumen of the invagination appears empty except for the rod and a delicate sleeve-like structure which surrounds it. The plasma membrane of the sperm cell lies in immediate contact with the acrosomal membrane over its whole outer surface. In its general organization, this molluscan acrosome shows a rather close homology with that of the annelid Hydroides.     

Ultrastructure of spermatozoa in Orthalicidae (Mollusca,Gastropoda, Stylommatophora) and its systematic implications

Sperm morphology of orthalicid gastropods Clessinia pagoda, Spixia tucumanensis, Plagiodontes daedaleus (Odontostominae) and Drymaeus hygrohylaeus, D. poecilus, Bostryx stelzneri (Bulimulinae) are examined and described for the first time using transmission electron microscopy. Spermatozoa show the general characteristic of Pulmonata: an acrosomal vesicle, sperm nucleus helical, mitochondrial derivative forming a continuous sheath with paracrystalline material and coarse fibers associated with axonemal doublets. Features in the acrosomal complex and shape of the nucleus distinguish orthalicid sperms from other stylommatophoran. The acrosomal pedestal is traversed by fine striations in all species examined except in S. tucumanensis. The structure and thickness of the perinuclear sheath with a single or double layer of electron-dense material ensheathing the nuclear apex is characteristic of the group. The presence of a subnuclear ring in Drymaeus, Bostryx and Clessinia species is also reported. A data matrix of eleven species per 34 characters (16 sperm plus 18 anatomical and shell characters) from orthalicids plus other stylommatophoran and systellommatophoran representative species was constructed. Three cladistic analyses (sperm-based, anatomical-based and a combined sperm + anatomical-based) were performed to test the phylogenetic potential of sperm ultrastructure in orthalicid systematics and understand how sperm characters affect the topology and resolution of the obtained trees. Stylommatophora resulted in a monophyletic clade in the sperm-based and in the combined-character analysis. Orthalicidae is monophyletic only in the combined-character cladogram. Within Orthalicidae, Odontostominae is recovered as a monophyletic clade in all analyses, while Bulimulinae is paraphyletic in all trees except in the combined phylogeny. The present study and cladistic analyses performed support the hypothesis that characters on sperm ultrastructure are informative for stylommatophoran systematic and phylogenetic approaches, providing synapomorphies at familiar, subfamiliar and generic level.     

Morphological identification of sperm receptors above egg microvilli in the polychaete, Neanthes japonica

A fine-structural study of sperm-egg interactions in the polychaete Neanthes japonica was carried out. Unfertilized eggs are surrounded by a chorion 0.6-0.7 micrometers thick. Oocyte microvilli are inserted into the inner layer of the chorion. The outer layers of the chorion are opened just above the tips of the microvilli, where a membrane vesicle (microvillus tip vesicle, about 0.2 micrometers in diameter) plugs the chorion's opening. During fertilization, the acrosomal process of the sperm fuses with an egg microvillus within 1 min of insemination. All the microvillus tip vesicles disappear from the chorion surface within 5 min of insemination. When eggs, which are prefixed with glutaraldehyde, are inseminated, numerous sperm undergoing the acrosome reactions attach to the eggs. In the majority of these sperm, the tip of acrosomal process which is coated with the acrosomal content, adhere to a microvillus tip vesicle. These findings suggest that the microvillus tip vesicle serves as a sperm receptor, which induces the acrosome reactions and adhere to the sperm acrosomal process. The adhesion of the acrosomal process to the microvillus tip vesicle seems to be a prerequisite event for its fusion with the microvillus.     

A study of factors involved in induction of the acrosomal reaction in sperm of the sea urchin, Arbacia punctulata.

Several factors involved in induction of the acrosomal reaction in sperm of the sea urchin, Arbacia punctulata, have been investigated quantitatively using a simple substrate film technique to monitor extension of the acrosomal process by electron microscopy. Verification of typical acrosomal process formation has been accomplished using thin sections. Sperm were found to undergo the acrosomal reaction in artificial sea water in the absence of egg jelly coat at pH values above 9.6. In the presence of egg jelly a high percentage of sperm react at pH 8.6. At this pH, the fraction of sperm that undergo the acrosomal reaction is directly proportional to the concentration of egg jelly. The Ca²⁺ ionophore A23187 induces the acrosomal reaction in the absence of egg jelly at pH 8.6. The proportion of sperm that react is dependent on the concentration of ionophore and on the concentration of Ca²⁺ in the medium. Pretreatment of sperm with low levels of La³⁺ ion, which is known to be a Ca²⁺ ion antagonist, results in inhibition of egg jelly induction of the acrosomal reaction. These findings suggest that there are marked similarities between the acrosomal reaction in sea urchin sperm and membrane fusion dependent secretory processes in other cell types.     

Comparative study of sperm ultrastructure of Donax hanleyanus and Donax gemmula (Bivalvia: Donacidae)

The ultrastructure of bivalve spermatozoa can be species‐specific and often provides important taxonomic traits for systematic reviews and phylogenetic reconstructions. Young individuals of the Donacidae species Donax hanleyanus are often identified as samples of Donax gemmula. Hence, the spermatozoa ultrastructure of both species was described in the present work, aiming to identify characters that could be useful for further taxonomic and phylogenetic analyses. D. hanleyanus and D. gemmula spermatozoa were different especially in relation to acrosomal characteristics and chromatin condensation. The spermatozoon produced by D. hanleyanus had a nucleus (exhibiting granular chromatin with a rope‐like appearance) capped by a long and conical acrosomal vesicle, which extended itself outward beyond the anterior nuclear fossa. Otherwise, the nucleus of the sperm cell of D. gemmula showed well‐compacted chromatin, and its acrosome, which was partially inserted into the anterior nuclear fossa, had a bubble‐like tip. In conclusion, the conspicuous ultra‐structural differences found between the spermatozoan morphologies were helpful for the discrimination of the species. In conclusion, our results suggest that analyses of sperm ultrastructure of the bivalves in the family Donacidae can be valuable to investigate their taxonomic relatedness. The present results also contribute to assess the monophyletic status of the family.