Sperm ultrastructure in Hemidonax pictus (Hemidonacidae, Bivalvia, Mollusca): comparison with other heterodonts, especially Cardiidae, Donacidae and Crassatelloidea

The systematic position and affinities of the marine bivalve genus Hemidonax (Heterodonta, Veneroida) are investigated using comparative sperm ultrastructure, with particular focus on the various groups to which this genus has been assigned [Donacidae (Tellinoidea), Cardiidae (Cardioidea) and Crassatellidae (Crassatelloidea)]. Ultrastructural examination (using transmission electron microscopy) reveals that Hemidonax pictus produces sperm of the aquasperm type, with a short, rounded-conical acrosomal vesicle, a short, barrel-shaped nucleus, a short midpiece (composed of two centrioles and four surrounding mitochondria) and a flagellum containing a conventional 9 + 2 pattern axoneme. The acrosomal vesicle exhibits a wedge-shaped, highly electron-dense, basal ring component, and less dense anterior component (including a thin, electron-lucent layer apically, which may prove to be a useful apomorphy for Hemidonax ). A loose, granular deposit of subacrosomal material is located within a narrow invagination traversing most of the length of the vesicle. Comparison with sperm of other heterodont bivalves shows no close connection between Hemidonax and the Donacidae (Tellinoidea) or with the Crassatellidae (or other crassatelloideans). Although certain Veneridae (Veneroidea) and Cardiidae (Cardioidea, especially Fragum ) show much better conformity in sperm morphology to that observed in Hemidonax , no complete match could be found among studied taxa. We conclude that Hemidonax should be retained in its own, previously introduced family Hemidonacidae, and the latter be placed incertae sedis within the Euheterodonta.  © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society , 2008, 153 , 325–347.     

Sperm ultrastructure in Kellia suborbicularis (Bivalvia: Galeommatoidea: Kellidae)

The sperm cells of Kellia suborbicularis are narrow with a short bullet‐shaped acrosome, a 5.0–5.5 µm long and 0.4–0.6 µm broad nucleus, and a short midpiece with a ring of five mitochondria. The disposition of the subacrosomal substance into a coronet‐like formation is unique, and the sperm structure offers no clue to the relationship between Kellia and other galeommatoidean genera. The possible significance of narrow elongate sperm for their entry into the brood pouch is discussed.     

Sperm ultrastructure of a member of the black coral family Aphanipathidae: Rhipidipathes reticulata (Anthozoa, Antipatharia)

Fertile male polyps of three colonies of the black coral Rhipidipathes reticulata (Aphanipathidae) from Togian Islands (Indonesia) have been the source of the sperm investigated at ultrastructural level, in order to compare their organization with that of other members belonging to the family Antipathidae and Myriopathidae. The extension of the studies to a representative of the family Aphanipathidae stresses once more the structural similarity of the male gametes in antipatharians. A sketch of the sperm model reports the similarity and differences in the examined taxa. Among the micro-characters, the cup-like body linked to the pericentriolar apparatus, is exclusive of the antipatharians. Other inclusions concern the more common pro-acrosomal vesicles or the acrosomelike structure observed only in Antipathella subpinnata and Myriopathes japonica. Lipid vesicles are occasionally present. A typical inclusion, the electron-dense content of which has a C-shaped configuration, is restricted to Rhipidipathes reticulata and is associated to the cup-like body or to the mitochondrion.     

Ciliary ultrastructure of protobranchs (Mollusca, Bivalvia)

Abstract. The external epithelial cilia and other surface structures of the nuculoid protobranchs Nuculana pernula and Nucula nitidosa were studied. The gill lamellae and labial palps are partly covered with very long cilia. These have a modified slender distal portion, an ordinary metazoan-type basal body, a basal foot. and a single, long cross-striated rootlet. In cilia on the gills of N. nitidosa , the basal foot is thick and attaches to the next basal body directly behind. Unciliated surface areas on the gills, labial palps, and foot are covered with a dense brushborder of microvilli. We observed no specific homologies between the cilia of the protobranchs studied and the epidermal cilia of the enigmatic Xenoturbella bocki , hence the recent hypothesis of a close connection of the latter to the protobranch bivalves is questioned.     

Reconstructing the Anomalodesmata (Mollusca: Bivalvia): morphology and molecules

The extant anomalodesmatan bivalves have always proved rather enigmatic and difficult to interpret, both in terms of their relationships to other bivalve taxa and the interrelationships of the constituent families. These difficulties stem from their diverse and often highly specialized life habits which have resulted in a wide array of disparate morphologies, and also from the fact that many are extremely rare. Classifications based on morphological characters have been dogged by fears that convergent and parallel evolution has masked phylogenetic signals. Molecular surveys of members of 12 of the 15 constituent families, using the 18S rRNA gene, have revealed that anomalodesmatans are robustly monophyletic and lie within the basal heterodonts. The Anomalodesmata should no longer be regarded as a subclass, but as a part of the Heterodonta. Here we present an enhanced analysis of 32 anomalodesmatan species (representatives of 12 families). Our results, subjected to Maximum Parsimony, Maximum Likelihood and Bayesian analyses, challenge our understanding of the internal relationships within the Anomalodesmata. In particular they indicate the need for a re-distribution of the families traditionally placed in the Thracioidea and Pandoroidea into a 'thraciid' lineage (Thraciidae + Cleidothaeridae + Myochamidae) and a 'lyonsiid' lineage (polyphyletic Lyonsiidae + Clavagellidae + Laternulidae + Pandoridae). The endolithic Clavagella and endobenthic Brechites and Penicillus form a robust clade. The hypothesis that the carnivorous septibranchs are monophyletic can, thus far, be neither supported nor rejected. Mapping critical morphological characters onto our molecular results provides evidence of multiple loss of some characters (e.g. prismato-nacreous shell microstructure and shell spicules) and also multiple gain of others (e.g. chondrophores).  © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society , 2006, 148 , 395–420.     

Sperm Ultrastructure of Two Mollusk Species Geukensia demissa and Modiolus modiolus (Mytilidae, Bivalvia)

Sperm ultrastructure was studied in two Atlantic species of bivalve mollusks Geukensia demissa and Modiolus modiolus (Mytilidae). These spermatozoa have a classic structure common for species with external fertilization: the head of the spermatozoon of G. demissa and M. modiolus consists of an acrosome, including an acrosomal vesicle and periacrosomal material, a nucleus, and a middle part with two mutually perpendicular centrioles, surrounded by a ring of spherical mitochondria. The spermatozoa of G. demissa and M. modiolus differ in the general shape and size of the head (M. modiolus, 5.8 × 4 m; G. demissa, 4.2 × 2.5 m), as well as the structure of the acrosome and the number of mitochondria (M. modiolus, 8–12; G. demissa, 5–6). The spermatozoa of the Atlantic species M. modiolus and M. modiolus (M. kurilensis) from the Sea of Japan are close in ultrastructure, but differ in the number of mitochondria. This could possibly be a reason to consider M. modiolus from the Sea of Japan as a separate subspecies, M. modiolus kurilensis. In ultrastructure, the spermatozoa of G. demissa differ significantly from the spermatozoa of M. modiolus, but are similar to the spermatozoa of species of the genus Brachidontes.     

Molecular phylogeny of pearl oysters and their relatives (Mollusca,Bivalvia, Pterioidea)

Background  

The superfamily Pterioidea is a morphologically and ecologically diverse lineage of epifaunal marine bivalves distributed throughout the tropical and subtropical continental shelf regions. This group includes commercially important pearl culture species and model organisms used for medical studies of biomineralization. Recent morphological treatment of selected pterioideans and molecular phylogenetic analyses of higher-level relationships in Bivalvia have challenged the traditional view that pterioidean families are monophyletic. This issue is examined here in light of molecular data sets composed of DNA sequences for nuclear and mitochondrial loci, and a published character data set of anatomical and shell morphological characters.     

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.     

Sperm ultrastructure in Chironomoidea (Insecta, Diptera)

The fine structure of spermatozoa from several species of chironomids, of Culicoides sp. (Ceratopogonidae) and of Odagmia pontina (Simulidae) was studied. A synapomorphic feature, consisting of nine kidney-shaped structures forming the centriole adjunct, was found in the chironomid species. All members of Chironomoidea share a mono-layered acrosome and a flagellar axoneme, provided with accessory tubules with 15 protofilaments in their tubular wall. The axoneme has a 9+9+2 pattern, but in an unidentified species of chironomid, a 9+9+0 model was observed where the central complex and the spokes are missing. Sperm motility is, however, maintained in all the examined species. The spermatozoa of this taxon have the tendency to complete maturation during their progression along the deferent ducts. Thus, in the proximal region of these ducts, they often show remnants of the spermatid cytoplasm.     

Yearly variation in recruitment and its effect on population dynamics inYoldia notabilis (Mollusca: Bivalvia), analyzed using projection matrix model

Long-term variation in recruitment was estimated by constructing projection matrices for a marine bivalve, Yoldia notabilis, at two stations in Otsuchi Bay, northeastern Japan, and the effects of its variation on population dynamics were examined using a simple matrix model. The matrix model was developed from the Leslie matrix, in which the population growth rate λ was expressed as a function of recruitment rate r₀. The equilibrium recruitment rate r_s, or the recruitment rate required to maintain population at constant size (λ=1), was expressed by the reciprocal of the reproductive value of a newly recruited individual. The estimates of r_s for the field population were lower at the shallower station than at the deeper station, reflecting higher survivorship and fecundity. Past recruitment rate estimated both by the field samplings for 3 years and by the back-calculation from the current age structure for over 10 years showed large yearly variation, ranging between 0 and 58.6×10⁻⁴. The estimates were larger than r_s, and hence, large enough to increase population size (λ>1) only in approximately one-third of the estimated years. This suggests that the population has been maintained by occasional successful recruitment occurring once every few years.     

Morphological perspective on the classification and evolution of Recent Pterioidea (Mollusca: Bivalvia)

The evolutionary relationships of the Recent Pterioidea are inferred from a phylogenetic analysis of representatives of all pterioidean genera based on original observations of anatomy and shell morphology, and an extensive survey of bivalve literature. The well-resolved cladogram supports monophyly for the superfamily, but renders all but one family (the monotypic Pulvinitidae) polyphyletic. In addition, these results reveal a considerable level of convergence and parallelisms through the Pterioidea. The branching order of pterioid genera in the morphological analysis is largely corroborated by the sequence of their appearance in the fossil record. The palaeontological evidence provides important information on dating lineage splitting events and transitional taxa. The proposed phylogeny integrates the cladistic analysis of the Recent Pterioidea with the fossil record and suggests that the crown-group pterioideans probably originated in the Triassic from the Bakevelliidae, an extinct paraphyletic stem group from which the Ostreoidea are also ultimately derived.  © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society , 2006, 148 , 253–312.     

Sperm ultrastructure in the nudibranch genus Halgerda with reference to other Discodorididae and to Chromodorididae (Mollusca: Opisthobranchia)

Comparative sperm ultrastructure within the molluscan nudibranch genus Halgerda (Discodorididae) was examined for the first time using transmission electron microscopy (TEM), based on 17 of the 35 known species. In addition, observations on two other discodorids are made to facilitate outgroup comparison with Halgerda, including one species of Discodoris (D. boholiensis) and Asteronotus cespitosus (currently accepted as the closest sister taxon to Halgerda). Comparison was also made with some genera of the Chromodorididae in view of sperm similarities. Spermatozoa of all species examined were of the complex, helical, elongate ( approximately 300-400 micro m) type characteristic of most heterobranch gastropods. These cells exhibit the following discrete regions (in anteroposterior sequence) : an acrosomal complex (composed of a rounded, membrane-bound vesicle and a column-like pedestal); a solid, helical nucleus; an elongate, helical midpiece (composed of an axoneme and associated nine coarse fibers, an enveloping mitochondrial derivative of matrix, and paracrystalline materials and glycogen helix); an annular complex; and a short glycogen piece. Of these regions, the midpiece is by far the longest, occupying over 90% of the total sperm length. Comparison with other members of the radula-bearing cryptobranch dorids reveals several sperm similarities to other genera in the clade, particularly those of other Discodorididae and also with the Chromodorididae. Comparison with previously studied genera reveals noteworthy sperm differences within the Discodorididae. The most notable differences are the internal structure of the acrosomal pedestal (long and homogeneous in Halgerda, Discodoris; short and homogeneous in Asteronotus; long and finely striated in Rostanga; oblong with angular electron-lucent striations in Jorunna) and the internal structure of the glycogen piece. The pronounced helical keels of most Halgerda and Discodoris nuclei contrast with the weakly helical nucleus of Asteronotus. Sperm features alone do not provide a means of defining the genus Halgerda or the family Discodorididae nor do they support the monophyletic status of the caryophyllidia-bearing dorids. Important sperm characters such as the acrosome, nucleus, and midpiece can often still be determined from specimens that have been initially fixed in formalin, then stored in ethanol for extended periods of time (i.e., museum material). Of all sperm features, the mitochondrial derivative of the midpiece is the most resistant to long-term fixation : the survival of acrosomal, nuclear, and axonemal components is variable, presumably a factor of prefixation autolysis, varied primary fixation times and temperatures, formalin quality, and duration of alcohol storage.     

Phylogeny of Veneroidea (Mollusca: Bivalvia) based on morphology and molecules

The largest Recent family of Bivalvia, the marine Veneridae with approximately 800 species, comprises one of the least understood and most poorly defined molluscan taxa, despite including some of the most economically important and abundant bivalves, for example quahog, Pismo clams, and Manila clams. A review of previous phylogenetic analyses including the superfamily Veneroidea (Veneridae, Petricolidae, Glauconomidae, Turtoniidae, Neoleptonidae) and within the Veneridae shows minimal taxon sampling leading to weak conclusions and few supported synapomorphies. New phylogenetic analyses on 114 taxa tested the monophyly of Veneroidea, Veneridae, and 17 nominal venerid subfamilies, using morphological (conchological, anatomical) data and molecular sequences from mitochondrial (16S, cytochrome oxidase I) and nuclear (28S, histone 3) genes. Morphological analyses using 45 exemplar taxa and 23 traditional characters were highly homoplastic and failed to reconstruct traditional veneroid classification. Full morphological analyses (31 characters) supported the monophyly of Veneroidea and Veneridae but only when certain taxa were excluded, revealing analytical difficulties caused by a suite of characters associated with neotenous or miniaturized morphology. Molecular analyses resulted in substantially higher clade consistency. The combined molecular data set resulted in significant support for a particular topology. The monophyly of Veneridae was supported only when Petricolidae and Turtoniidae were subsumed, and recognized as members with derived or neotenous morphologies, respectively. Morphological character mapping on molecular trees retained a high level of homoplasy, but revealed synapomorphies for major branch points and supported six subfamily groups (Dosiniinae, Gemminae, Samarangiinae, Sunettinae, Tapetinae, combined Chioninae + Venerinae). Glauconomidae and Neoleptonidae are provisionally maintained in Veneroidea pending further study; Petricolinae and Turtoniinae are placed in Veneridae. © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society, 2006, 148 , 439–521.     

Molecular phylogeny of Anomalodesmata (Mollusca: Bivalvia) inferred from 18S rRNA sequences

The origin of the anomalodesmatan bivalves and the relationships of the constituent families are far from being settled. Phylogenetic uncertainties result from the morphological heterogeneity of the Anomalodesmata and from parallel/convergent evolution of several character complexes due to similar life habits. Here, we assess these problems with 26 near-complete anomalodesmatan 18S rRNA sequences from 12 out of 15 families and a selection of heteroconch outgroup taxa. The robustly monophyletic Anomalodesmata share insertions in the V2 and V4 expansion regions. Both parsimony and maximum-likelihood analyses confirm their position among the basal heterodonts rooting between Carditidae and Lucinidae or, together with the latter, between Carditidae and the remaining Heterodonta. There is no support for monophyletic Myoida, nor for a close relationship of Anomalodesmata with any myoid taxon. At the base of the Anomalodesmata is an unstable cluster of long-branch species belonging to the Poromyidae, Verticordiidae, Lyonsiellidae and Thraciidae. The remaining Anomalodesmata split consistently but with varying branch support into three major clades: the Cuspidariidae excluding Myonera ; a 'thraciid' clade consisting of (Euciroidae, ( Myonera ( Thracia, Cleidothaerus , Myochamidae))); and a 'lyonsiid' clade with Laternulidae, Pandoridae, diphyletic Lyonsiidae due to a robust clade of Lyonsia norwegica and the clavagellid Brechites vaginiferus . Tests of various alternative topologies showed that all are significantly longer but optimal likelihood trees with monophyletic carnivorous taxa and/or Thraciidae are not significantly less likely. These results differ greatly from previous morphological studies. Palaeontological data and homology decisions for selected characters are evaluated in the light of the molecular trees.  © 2003 The Linnean Society of London, Zoological Journal of the Linnean Society , 2003, 139 , 229–246.     

The muscular system of Musellifer delamarei (Renaud-Mornant, 1968) and other chaetonotidans with implications for the phylogeny and systematization of the Paucitubulatina (Gastrotricha)

We studied comparatively the muscle organization of several gastrotrich species, aiming at shedding some light on the evolutionary relationships among the taxa of the suborder Paucitubulatina. Under confocal laser scanning microscope, the circular muscles were present in the splanchnic position as incomplete circular rings in Musellifer delamarei (Chaetonotidae) and Xenotrichula intermedia (Xenotrichulidae) and as dorsoventral bands in Xenotrichula punctata, Heteroxenotrichula squamosa and Draculiciteria tesselata (Xenotrichulidae); in the somatic position, M. delamarei shares the presence of dorsoventral muscles with all the Xenotrichulidae, in contrast with the remaining Chaetonotidae that lack these muscles. Maximum parsimony analysis of the muscular characters confirmed monophyly of Paucitubulatina and Xenotrichulidae, while the Chaetonotidae was paraphyletic, with the exclusion of Musellifer , which is the most basal genus within the Paucitubulatina. Xenotrichulidae is the sister taxon to Chaetonotidae, which in turn has Polymerurus as the most basal taxon. In general, the results agree with recent phylogenetic inferences based on molecular characters and support the hypothesis that, within Paucitubulatina, dorsoventral muscles are plesiomorphies retained in marine, interstitial, hermaphroditic gastrotrichs. Dorsoventral muscles were subsequently lost during changes in lifestyle and reproduction modality that took place with the invasion of the freshwater environment. This new information prompted us to reconsider the systematization of Chaetonotidae, proposing the establishment of Muselliferidae fam. nov. to include the genera Musellifer and Diuronotus .  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 379–398.     

Ultrastructure of Sperm in <Emphasis Type="Italic">Mercenaria stimpsoni</Emphasis> and <Emphasis Type="Italic">Mactra chinensis</Emphasis> (Mollusca: Bivalvia) from the Sea of Japan

The ultrastructure of the sperm of the common bivalve species Mercenaria stimpsoni and Mactra chinensis from Peter the Great Bay is described. The sperm structure is typical for animals with external insemination. The sperm consists of a head, middle part, and flagellum. The sperm head of M. stimpsoni has a curved crescent form and includes the nucleus and acrosome; the head length is 9.8 μm. The acrosome is subdivided to the acrosome granule and the periacrosomal material. There are 4 mitochondria of about 0.8 μm in size in the middle part of the spermatozoon. The mitochondria surround the centriolar apparatus, which consists of proximal and distal centrioles located at a right angle. The axoneme originates from the distal centriole. The sperm of M. chinensis is barrel-shaped, with a head length of 3.2 μm. The acrosome is relatively larger, and its height is 1–1.2 μm. There are also 4 mitochondria 0.6–0.8 μm in the middle part of the spermatozoon. The sperm structure of the described species is typical of the families to which the mollusks belong, with insignificant variations.     

Phylogeny of Early Cretaceous spatangoids (Echinodermata: Echinoidea) and taxonomic implications

A phylogenetic analysis of 36 species provides a test for the taxonomy and the history of Early Cretaceous spatangoids. Most taxonomic units from genera to suborders are consistent with the proposed phylogenetic framework. We retain Hemiasterina, Micrasterina, Hemiasteridae, Schizasteridae, Hemiaster , Heteraster , Mecaster , and Periaster as original monophyletic groups. However, all of these clades originate without the classical apomorphies normally ascribed to them. We suggest a revision of their diagnoses and of the generic attributions of basal species. Some ill-defined, 'primitive', and paraphyletic taxa are recognised: Toxaster , Epiaster , Palhemiaster , and Toxasteridae. Even if they do not have phylogenetic meaning, they are retained here, pending a more complete revision.     

Fine structure of the early stages of spermatogenesis in the Pacific oyster, Crassostrea gigas (Mollusca, Bivalvia)

The aim of this study is to describe the early stages of spermatogenesis of the Pacific oyster Crassostrea gigas using both light and electron microscopy. The gonad is formed by gonadal tubules invaginated in a connective tissue constituting a storage tissue. Myoepithelial cells surround each gonadal tubule and are associated with an acellular matrix delimiting the outer part of the tubule, the inner part is composed by intragonadal somatic cells associated with germinal lineage. Two types of spermatogonia are identified, where type I spermatogonia (Spg I) are large, scarce and pale cells leaned against the base of the tubule (nuclear diameter: 5.5+/-0.5 microm). Type II spermatogonia (Spg II) are clustered and dark cells which appear smaller than type I (nuclear diameter: 4.3+/-0.3 microm). The aspect of nuage-like material in cytoplasm is described from pale spermatogonia to primary spermatocytes (nuclear diameter: pachytene 3.6+/-0.3 microm, diplotene 3.4+/-0.3 microm), while no structure related to a chromatoid body was observed in oyster spermatocytes and spermatids.     

Rib fabrication in Ostreoidea and Plicatuloidea (Bivalvia,Pteriomorphia) and its evolutionary significance

Ribs of Ostreoidea and Plicatuloidea are defined as antimarginal, that is, perpendicular to the margin throughout growth. Morphogenetically, these ribs are unique, since, unlike radial ribs, they are secreted by a homogeneous mantle margin. Based also on the reconstructed shell secretion cycle in Bivalvia, we propose that ribs of Ostreoidea and Plicatuloidea are formed by a mantle margin which, upon extension from the shell margin, stretches and folds by taking the preformed ribs as templates. In extending perpendicular to the margin (as in all Bivalvia growing isometrically), such a mantle extends the rib pattern antimarginally. Ribs of this kind are purely mechanical structures, as their arrangement depends on the mechanical properties of the mantle and on the environmental conditions. This explains the high irregularity of such ribbing patterns. The presence of antimarginal ribs in both the Ostreoidea and Plicatuloidea sheds light on their origin. The first known oyster, Actinostreon cristadifformis, probably derived from an antimarginally ribbed Prospondylidae gen. indet. in the Late Permian or Early Triassic. Antimarginally ribbed Triassic species formerly included in Placunopsis originated both the Dimyidae Atreta in the Late Triassic and Enantiostreon in the Mid Triassic, which was transitional to Plicatulidae. Therefore, Dimyidae and Plicatulidae are closely connected and grouped under Plicatuloidea, to which Ostreoidea is phylogenetically unrelated.     

Cytological evidence for self-fertilization in Lasaea subviridis (Galeommatacea: Bivalvia)

Summary

Isolated individuals of Lasaea subviridis simultaneously spawn both eggs and sperm. The sperm attach to the eggs by undergoing an acrosomal reaction and a male pronucleus is incorporated into the egg cytoplasm. Two reduction divisions associated with the production of two polar bodies occur before the first cleavage. These results are consistent with self-fertilization, but not with apomictic or meiotic parthenogenesis. The net fertilization efficiency of Lasaea subviridis natural populations is estimated at 99.93%.