Oogenesis in the marine mussel Mytilus edulis: an ultrastructural study

Ultrastructural changes occurring during the course of development in oocytes of Mytilus edulis are described for mussels collected at monthly intervals over a period of one year (September 1981 to October 1982) from a site in Cornwall, England. During early stages of oogenesis the oocyte is surrounded by a small number of follicle cells but, as development proceeds, the follicle cells are restricted to the stalk region which attaches the oocyte to the acinar wall. Contact between the follicle cells and the developing oocyte is maintained by means of desmosomelike gap junctions. Organelles and inclusion bodies present in the ooplasm during oogenesis include rough endoplasmic reticulum (RER), Golgi bodies, mitochondria, free ribosomes, Balbiani's vitelline body, annulate lamellae and yolk and cortical granules. The RER, in particular, varies considerably throughout the course of development. Evidence for uptake of exogenous macromolecules into oocytes by pinocytosis is presented; it occurs in the basal region of previtellogenic oocytes prior to the formation of the vittelline coat. Lipid-yolk granules invariably have mitochondria in close association and, during the winter months, develop in close proximity to small, apparently glycogen-rich vesicles possibly suggesting that conversion of glycogen to lipid takes place in developing oocytes. Oocyte degeneration was commonly observed and involves initial breakdown of the plasma membrane followed by rupture of the vitelline coat. The oocyte contents once released into the acinar lumen are resorbed by the epithelial cells of the gonoducts, which are prevalent throughout the mantle of ripe individuals.     

Multiple trans-Arctic passages in the red alga Phycodrys rubens: evidence from nuclear rDNA ITS sequences

In order to investigate how episodes of geological and climatic change have influenced the distribution and evolutionary diversification of Arctic to cold temperate-North Atlantic seaweed species, intraspecific genetic variation was analyzed among isolates of the sublittoral, benthic red alga Phycodrys rubens (collected between June 1992 and January 1994). Rooted phylogenetic analyses of nuclear ribosomal DNA internal transcribed spacer (ITS) sequences and the plastid encoded Rubisco spacer sequences suggest that P. rubens invaded the North Atlantic from the Pacific shortly after the opening of the Bering Strait (3 to 3.5 million years ago), colonizing both the western and eastern Atlantic coasts. Based on these data we further hypothesize that P. rubens survived along the European coasts during the more recent Pleistocene glaciations, while becoming locally extinct along the North American Atlantic coasts. Following retraction of the last ice sheet, the western Atlantic coast was colonized a second time from the Pacific. The presence of two distinct genetic types (based on ITS and Rubisco sequences) along the European coasts is postulated to be a result of isolation and subsequent differentiation. This is likely because ice-free areas are known to have existed in northern Scotland and Norway during the last glaciation. The presence of an East Atlantic genetic type along the West Atlantic coast is believed to be a recent introduction (caused by human activity) of P. rubens to Newfoundland.     

Introduced versus native subspecies of Codium fragile: how distinctive is the invasive subspecies tomentosoides?

After its introduction, the green alga Codium fragile (Sur.) Hariot ssp. tomentosoides (van Goor) Silva has spread widely on several temperate-zone, rocky shores where non-weedy conspecific subspecies occur (N.E. Atlantic, N.E. Pacific, S. Pacific). To determine how phenologically and morphologically distinctive the invasive alga was relative to native subspecies, I compared marine intertidal populations of C. fragile ssp. tomentosoides and the native C. fragile ssp. novaezelandiae (J. Ag.) Silva (hereafter referred to as ssp. tomentosoides and ssp. novae-zelandiae respectively on New Zealand shores in 1992, 1993 and 1995. On the North Island, the invasive ssp. tomentosoides is sparsely distributed on low intertidal benches on wave-protected shores in the Hauraki Gulf (east coast) in spring and summer, and thalli die back to the perennial holdfast in autumn. In contrast, the native ssp. novaezelandiae forms dense beds within the low intertidal mussel zone on wave-swept shores of Maori Bay (west coast), and fronds are perennial. Whereas ssp. tomentosoides has only a few fronds arising from the spongy basal hold-fast, ssp. novae-zelandiae thalli are composed of many fronds. The ssp. tomentosoides from the Hauraki Gulf is significantly more branched than comparably sized native conspecifics from Maori Bay. These phenological and morphological differences were used to predict the subspecific identity of C. fragile from three other locations on the North Island, two locations on the South Island, and four locations on S.E. Australian shores; microscopic examination of utricles was used to check the predictions. Seasonality and number of fronds per thallus are the most reliable characters for field identification of native vs invasive subspecies: perennial intertidal thalli with large numbers of fronds are indicative of native subspecies for different geographic regions.     

Ultrastructure changes in hepatocytes of catfish Clarias gariepinus from Lake Mariut, Egypt

In the present study, specimens of catfish (Clariidae) were collected from a polluted location (Main Basin) and a relatively clean area (East Basin) in Lake Mariut, one of the Nile Delta Lakes in Egypt. Fifteen fish were taken from each site. Liver preparations of fish from the two sources were comparatively examined for cellular changes using transmission electron microscopy. Fish hepatocytes from the polluted area showed accumulation of the heterochromatin, enlarged nucleoli, and an extremely folded nuclear envelope. Perichromatin granules were increased and progressively formed small clusters closely associated with patches of heterochromatin. In the cytoplasm, fractionation, dilation, and vesiculation of rough endoplasmic reticulum (RER), and elevated amounts of smooth endoplasmic reticulum (SER) tubules were noted. The most frequent pathological modifications were the swelling of mitochondria, cristae regression and changes in the electron-transparency of the matrix. Lysosomes showing myelin-like stacks of membraneous material (phospholipidosis), glycogenosomes (i.e., glycogen rosettes enclosed by membranes) and cytoplasmic myelinated bodies were strongly developed. Furthermore, increasing numbers of secondary lysosomes with degraded cell organelles were found. With reference to the storage vesicles, there appeared to be an increase in the lipid droplets (lipidosis) within many hepatocytes. This study reinforces the need to select representative sentinel species from different habitats for biomonitoring purposes and it provides further support for the use of biomarkers in assessing the health of aquatic ecosystems.     

Ovarian morphology and oogenesis in Aurelia aurita (Scyphozoa: Semaeostomae): ultrastructural evidence of heterosynthetic yolk formation in a primitive metazoan

In Aurelia aurita, the ovaries arise as horseshoe-shaped evaginations of the gastrodermis in the floor of four interradial gastric pouches. Germ-cell islands arise within endodermally-derived gastrodermal cells. Oocytes grow and gradually bulge into the mesoglea while maintaining physical contact throughout vitellogenesis with specialized cells called trophocytes. Ultrastructural changes suggest that these cells transport yolk precursors from the coelenteron to the oocytes in a manner similar to that reported for the trophonema cells of anthozoan ovaries. Vitellogenesis involves both the autosynthetic activity of the oocyte organelles (Golgi complex and rough endoplasmic reticulum) and the heterosynthetic incorporation of precursors through endocytotic processes involving both coated pits and vesicles and smooth-surfaced tubules. Ultrastructural data suggest that different types or classes of yolk precursors enter the oocyte through the trophocytes and via the surrounding mesoglea. To our knowledge, this is the most primitive animal in which this type of yolk synthesis has been described. The trophocyte-oocyte relationship in oocytes of A. aurita is reminiscent of the trophonema-oocyte relationship in anthozoans and supports the belief that the Anthozoa and Scyphozoa share a close phylogenetic relationship.     

Ultrastructure of oogenesis in the holopelagic polychaetes Rhynchonerella angelini and Alciopa reynaudii (Polychaeta: Alciopidae)

Ultrastructural features of oogenesis were examined in the pelagic polychaetes Rhynchonerella angelini and Alciopa reynaudii which were collected from Bahamian waters by a manned submersible during 1979 and 1980. No definitive ovary was detected in either species. Oogonia are released into the coelom as packets of cells, where they undergo mitotic division while surrounded by an envelope of sheath cells. Cytokinesis is incomplete, resulting in intercellular bridges between oogonia. Oocytes undergo early stages of meiosis characterized by the presence of synapsed chromosomes, followed by a period of rapid cytoplasmic and nuclear growth. Oocytes are released from the packets in the early vitellogenic phase into the coelom, where they undergo yolk synthesis as solitary coelomic cells. Vitellogenesis includes both autosynthetic and heterosynthetic processes. Autosynthesis involves the fusion of secretory vesicles formed by the combined activity of the rough endoplasmic reticulum and Golgi complex, with convoluted electron-dense tubular bodies of unknown origin. Heterosynthesis involves the intense uptake of exogenous precursors through endocytosis and their fusion into nascent yolk bodies which, in turn, are presumed to fuse with autosynthetically-derived yolk bodies. No nutrient stores were detected in somatic tissues. Early and middle stages of vitellogenic oocytes were absent from the coelom. This absence combined with the high level of endocytotic activity suggests that vitellogenesis occurs rapidly. These features, in combination with the presence of an exceptionally thin body wall and gut, might serve as related adaptations for predator avoidance by the maintenance of relatively low tissue-density. Alciopid, phyllodocid, and nereid polychaetes share some common reproductive features including the presence of dispersed ovaries, clusters of syncytial germ cells which undergo meiosis while enveloped by somatic cells and the release of oocytes from the clusters prior to vitellogenesis.     

A comparative seasonal study of two populations of Hypnea musciformis from the East and West Coasts of Florida,USA I. Growth and chemistry

Dry weight levels of the red alga Hypnea musciformis (Wulfen) Lamouroux from Atlantic and Gulf of Mexico coastal sites in florida, USA were lowest in the late winter and early spring, increasing through the summer and highest in the fall. There was a two-month lag in the Gulf coast population's dry weight pattern, indicating differing growth patterns. Chlorophyll a, phycoerythrin and phycoerythrin/chlorophyll a ratios were highest in the winter and lowest in the summer for both populations. Total pigment levels for H. musciformis from the Atlantic coast site were significantly greater than those of the Gulf coast. Protein and carbohydrate percentages were inversely related in both populations, with carbohydrate levels highest in summer and protein levels highest in winter. The Gulf coast population contained significantly more protein than the Atlantic coast plants. Carrageenan levels were highest in spring and lowest in fall, the Atlantic coast population generally had higher levels than the Gulf coast population. The differences in seasonal patterns and levels of the chemical constituents were reflected by distinct morphological characteristics for each population. The Atlantic coast population was larger, darker, more coarse in texture and possessed more crozier branch tips than the Gulf coast plants. These distinctions represent acclimitization responses that relate to habitat differences.     

An electron-microscope study of periostracum formation in some marine bivalves. II. The cells lining the periostracal groove

The histology and ultrastructure of the epithelial cells of the outer and middle mantle folds of the bivalves Mytilus edulis (L), Cardium edule (L), Macoma balthica (L) and Nucula sulcata Bronn are described. The cells lining the inner face of the outer fold exhibit a prominent granular endoplasmic reticulum, and Golgi complexes which are concerned with the elaboration of granules and vesicles eventually incorporated into the periostracum. A gradual reduction in the protein synthetic apparatus occurs towards the tip of the fold. Within the cells, it is proposed that the ovoid inclusion bodies are lysosomes and that they control the rate of secretion. The cells of the middle fold are cuboidal in appearance. Those of M. edulis and N. sulcata exhibit prominent granules, whereas those of C. edule and M. balthica possess vesicles. The cells of M. edulis differ from the others in possessing stout bundles of filaments, which occupy large areas of the cell and constitute a cell web. The cells of the epithelium in all cases do not appear to be implicated in periostracum formation.     

Ultrastructural responses and oxidative stress induced by cypermethrin in the liver of Labeo rohita

The present study was conducted to establish the relationship between selected oxidative stress parameters and ultrastructural responses in liver tissue of Labeo rohita fingerlings exposed to cypermethrin. Fish were exposed to lethal (4.0 μg L^?1) and sublethal (0.4 μg L^?1) concentrations of cypermethrin for a period of 24, 48, 72 and 96 h for acute studies and 1, 5, 10 and 15 days for subacute studies, respectively. Results showed increased catalase (CAT) and protease activity, hydrogen peroxide (H₂O₂), malondialdehyde (MDA), protein carbonyls and free amino acid (FAA) levels at both concentrations. This suggests participation of free-radical-induced oxidative cell injury in mediating the hepatotoxicity of cypermethrin. In corroboration of this, ultrastructural lesions witnessed a reduction in the number of cell organelles, swollen, vacuolated and condensed mitochondria, dilated rough endoplasmic reticulum, and reduced numbers of smooth enodplasmic reticulum, peroxisomes and lysosomes at the lethal (4.0 μg L^?1) concentration. At the sublethal (0.4 μg L^?1) concentration, cytoplasmic vacuolation, condensed, vacuolated and swollen mitochondria, dilated rough endoplasmic reticulum and an absence of hepatocyte microvilli were prominent. Ultrastructural changes were exhibited as subcellular responses due to the imbalance in cellular oxidative status by means of oxidative damage.     

Confirmation of serial spawning in the chokka squid Loligo vulgaris reynaudii off the coast of South Africa

Ovary maturation and spawning in the chokka squid Loligo vulgaris reynaudii were investigated by collecting squid from across their distributional range on the southeastern coast of South Africa between 1992 and 1993. Based on histological examination of the ovarian tissue and the separation of multiple modes in oocyte size-frequency distribution, ovary development was characterised by eight distinct stages. Our study confirms serial spawning in L. v. reynaudii. Received: 9 October 1998 / Accepted: 22 April 1999     

The ultrastructure of epidermal mucous cells in marine invertebrates (Nemertini,Polychaeta, Prosobranchia,Opisthobranchia)

The epidermal mucous cells of various nemerteans, polychaetes and gastropods exhibit a highly heterogeneous fine structure, which is not correlated to systematic position or way of living. Formation and extrusion of the mucus secretory substances also follow different patterns. In the majority of species investigated, the mucus inclusions originate in the Golgi area, in Pomatias they form in the rough endoplasmic reticulum. The mucus droplets either coalesce in the cytoplasm or retain their individuality before being extruded.Supported by the Deutsche Forschungsgemeinschaft (Sto 75/2, We 380/4).     

Route of egg yolk protein uptake in the oocytes of kuruma prawn,Penaeus japonicus

The route of egg yolk protein uptake into the oocytes of kuruma prawn, Penaeus japonicus, was studied using immunohistochemical and electron microscopical methods. Although a significant immunofluorescence with anti-vitellin-immunoglobulin was observed in the enlarged follicle cells surrounding oil globule stage oocytes of the early vitellogenic ovary, no fluorescence was detected in shrunken follicle cells surrounding oocytes in the yolk granule stage. Electron microscopically, yolk granule stage oocytes have an irregular surface with numerous well-developed microvilli. In contrast, the surface of follicle cells is relatively smooth. The irregular surface of yolk granule stage oocytes was covered with a layer of electron dense material. Similar dense material was found in the spaces between the neighboring follicle cells on the yolk granule stage oocytes. The outer surface of the follicle cells on yolk granule stage oocytes was covered by dense materials which were similar to those found on the irregular surface of oocytes. Micropinocytotic vesicles containing dense material were found in the ooplasm near the irregular surface with numerous well-developed microvilli. Dense material was concentrated in the peripheral part of the small forming yolk bodies of yolk granule stage oocytes. This suggests that the electron dense material, probably egg yolk protein, transferred to the surface of yolk granule stage oocytes from the spaces between the neighboring follicle cells may be incorporated into the ooplasm by pinocytosis through the microvilli and subsequently aggregate to form yolk bodies.     

Mitochondrial DNA variation in king mackerel (Scomberomorus cavalla) from the western Atlantic Ocean and Gulf of Mexico

King mackerel (Scomberomorus cavalla Cuvier) collected in 1992 and 1993 from 13 localities along the Atlantic coast of the southeastern USA and in the northern Gulf of Mexico were surveyed for variation in mitochondrial (mt)DNA and a nuclear-encoded dipeptidase locus (PEPA-2). Both polymorphic and fixed mtDNA restriction sites were identified and mapped using conventional and polymerase chain-reaction (PCR)-based methods. Heterogeneity in mtDNA haplotype frequencies was found only in comparisons of pooled haplotypes from Atlantic localities versus pooled haplotypes from Gulf localities. This finding indicates weak genetic divergence between king mackerel from the Atlantic and those from the Gulf. Frequencies of two PEPA-2 alleles essentially paralleled previous findings: one allele (PEPA-2a) was common among samples from western Gulf localities, whereas the other allele (PEPA-2b) was common among samples from Atlantic and eastern Gulf localities. There was considerable variation in PEPA-2 allele frequencies within broadly-defined regions. Variation in mtDNA haplotypes and PEPA-2 genotypes was independent, as was variation in mtDNA haplotypes with sex or age of individuals. Variation in PEPA-2 genotypes was not independent of sex or age of individuals. The latter result suggests that frequencies of PEPA-2 alleles in samples of king mackerel may stem, in part, from sex and age distributions of individuals within samples, and indicates that caution should be exercised in using allelic variation at PEPA-2 as a measure of population (stock) structure in king mackerel. The discordance in spatial patterning of mtDNA haplotypes versus PEPA-2 alleles across the Gulf (i.e. homogeneity in mtDNA haplotype frequencies versus heterogeneity in PEPA-2 allele frequencies) may be due to either female excess at several localities, sex-biased migration, or both. Observed patterns of genetic variation also are consistent with the hypothesis that king mackerel in the western Atlantic may have been subdivided during Pleistocene glaciation, and that the current distribution of PEPA-2 alleles may be a historical artefact. Received: 17 December 1996 / Accepted: 2 April 1997     

Gametogenesis,embryogenesis, and larval features of the oviparous sponge <Emphasis Type="Italic">Petrosia ficiformis</Emphasis> (Haplosclerida,Demospongiae)

This study describes the reproductive cycle of Petrosia ficiformis and documents for the first time embryogenesis in an oviparous haplosclerid demosponge. Gonochoric adults, occurring in 2:1 female/male ratios, spawned in late autumn, after a 7-month long oogenesis and a 2.5-week-long spermatogenesis. Following a remarkable migration, the oocytes were released as 250 μm eggs bearing attached polar bodies and a thin mucous cover. Round-headed spermatozoa with three large mitochondria, and many proacrosomal vesicles fertilized the eggs externally. A fertilization membrane appeared around the zygotes. Nearly equal and total cleavage led to a stereoblastula that subsequently became an entirely ciliated larva. The larva alternated spherical and multilobate body shape and consisted of undifferentiated cells. It had poor abilities to swim and glide, probably experiencing passive dispersal and unselective attachment. Settlers developed choanocyte chambers after 1.5 months. Symbiotic microbes were absent from gametes and larvae, being necessarily acquired from the ambient at each sponge generation. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Spermatogenesis inPyrosoma atlanticum (Tunicata: Thaliacea: Pyrosomatida): Implications for tunicate phylogeny

Colonies ofPyrosoma atlanticum were collected by submersible in October 1988 in the Caribbean Sea, and testes were studied by electron microscopy. Spermatogonia, spermatocytes and early spermatids have two centrioles. The proximal centriole subsequently disappears, its remains apparently persisting in the spermatozoon as dense material adjacent to the distal centriole, which gives rise to the axoneme. At the tip of early spermatids are several 50 nm proacrosomal vesicles, which disappear leaving no trace in early elongating spermatids. The spermatozoon lacks an acrosome and has a head 35µm long. The head is differentiated into a bulbous posterior portion 5µm long × 1µm wide, a thinner anterior portion 25µm long tapering from a width of 0.7µm to a width of 0.4µm, and a very thin anterior extension 5µm long × 0.5µm wide. At the start of elongation, the anterior extension begins to form just lateral to the proacrosomal vesicles as a spiral projection comprising part of the nucleus, covered by a thin sheath of cytoplasm. This sheath of cytoplasm undergoes a complex differentiation. Ultimately, the nucleus in the anterior extension is overlain by two membrane-bound sheaths of cytoplasm connected by a spiral flange of cytoplasm. Between these two sheaths is a spiral space, open to the exterior through a subterminal pore near the sperm tip. In early spermatids the mitochondria fuse into a single mitochondrion, which remains lateral to the nucleus. The cristae become modified late in spermatogenesis. Throughout elongation of the spermatid there are patches of dense material between the nucleus and mitochondrion. A manchette of microtubules transiently encircles the thin anterior portion of the nucleus during the last phase of elongation. A manchette is not present during most of elongation. In the spermatozoon the mitochondrion, which has reticulate cristae, spirals a few times about the nucleus and extends from the junction between the bulbous portion and the thinner anterior portion of the nucleus to the junction between the thinner anterior portion and the nuclear extension. Spermatogenesis inP. atlanticum, compared to that in other tunicates, most closely resembles that in colonial ascidians, and supports the majority view that pyrosomes arose from aplousobranch ascidians that lost their attachment to the substratum. Pyrosome sperm are more highly derived than doliolid sperm, which have an acrosome that is probably capable of exocytosis. When salp and pyrosome sperm are compared, both are highly derived, but neither shares any apomorphies with the other that it does not share with at least one other tunicate order. Thus, sperm morphology does not support the majority view that pyrosomes gave rise to doliolids and neither confirms nor denies the idea that pyrosomes are intermediate between aplousobranch ascidians and salps. Therefore, it is likely that the class Thaliacea is polyphyletic, with doliolids arising very early from the ascidian lineage and with salps and pyrosomes arising somewhat later.     

Effects of zinc on epidermal ultrastructure in the larva of Clupea harengus

In March, 1983 changes in epidermal ultrastructure were examined in Clupea harengus L. larvae hatched from eggs incubated in four zinc concentrations (0.5 2.0, 6.0 and 12.0 ppm). In addition to the outer and inner epidermal cell types described previously, a third type of cell is present. Ultrastructurally this resembles the epidermal chloride cells of Sardinops caerulea Girard, characterised by numerous mitochondria, extensive smooth endoplasmic reticulum and a free surface exposed to the environment. These cells occur on the yolk sac, head and in the regions of the trunk just above the yolk sac. In larvae treated in 12.0 ppm zinc, the cells contain fewer mitochondria with fewer cristae than those in the controls. Smooth endoplasmic reticulum is much reduced forming nodular masses and contains granular osmiophilic inclusions. In larvae hatching from eggs previously incubated in 6.0 and 12.0 ppm zinc, the epidermal cells contain more vesicles, intracellular spaces, and swollen mitochondria and show signs of necrosis. The viability of these larvae is discussed.     

日本沼虾三种细胞器在精子发生过程中变化的研究

应用透射电镜技术,研究了日本沼虾在精子发生过程中线粒体、溶酶体及内质网的变化．从精原细胞到精子,生精细胞内线粒体数量逐渐增多,结构渐趋复杂化,并形成衍生物,参与精子顶体的形成．溶酶体从初级溶酶体逐渐形成次级溶酶体,其中包括包裹溶酶体及溶噬体;部分溶酶体构成精子顶体的一部分．精子发生的全过程中,未见典型的粗面内质网（ＲＥＲ）,仅见泡状粗面内质网（ＶＲＥＲ）;滑面内质网只在精原细胞期出现．支持细胞的作用包括两个方面：一为支持作用,使生精细胞有一个适宜的发育场所;二为营养作用,为生精细胞的发育提供足够的物质和能量．     

Gonadal morphology and gametogenesis in the sea pen Pennatula aculeata (Anthozoa: Pennatulacea) from the Gulf of Maine

The ultrastructural features of gametogenesis are described in male and female colonies of the sea pen Pennatula aculeata. Specimens were collected for observation and fixation at 113 to 231 m depth in the Gulf of Maine, USA, in August 1993. The species is gonochoric, and all stages of gametogenesis are observed in both male and female colonies >45 mm in height. Gametogenesis shows several features that differ from sea anemones. The developing oocytes and sperm cysts are completely encompassed by gastrodermally derived follicle cells, and they are released from the mesenteries into the coelenteron before they are fully differentiated. Following maturation in the coelenteron, the eggs and intact sperm cysts are expelled through the mouths of the autozoids during spawning. The expulsion of sperm cysts suggests that they function as primitive spermatophores, perhaps as a way of reducing sperm dilution. Vitellogenesis results in the biosynthesis of lipid droplets which are the sole nutrient reserves in the egg. Heterosynthetic vitellogenesis is characterized by the importation of lipid precursors into the oocyte, and there is some indirect evidence that hypertrophic follicle cells play a role in production, transport, and/or mediation of these precursors. Spermatogenesis is similar to that of other anthozoans. The spermatozoon has a cone-shaped head, a posterior nuclear fossa, a ring of lipid-like bodies in the midpiece, a prominent cytoplasmic collar surrounding the proximal flagellum, and a single mitochondrion, but the posterior region of the sperm also contains previously undescribed concentric rings of cisternae resembling smooth endoplasmic reticulum. Received: 23 March 1998 / Accepted: 31 July 1998     

Ultrastructural and cytochemical study on interactions between nutrient storage cells and gametogenesis in the mussel Mytilus edulis

The ultrastructural morphology of storage-cell breakdown and replenishment in Mytilus edulis is described for mussels collected at monthly intervals over a period of one year (September 1981 to October 1982) from a site in Cornwall, England. In addition cytochemical staining reactions at light and electron microscope levels are described for the storage cells and the Sertoli cells. The breakdown of adipogranular (ADG) cell components is believed to be a lysosomally-mediated process of controlled autolysis involving fusion of primary lysosomes with the protein granules. Increasing activity for lysosomal enzymes during ADG cell breakdown is demonstrated using quantitative cytochemistry. The presence of glycogen in vesicular connective tissue (VCT) cells is demonstrated using freeze-dried, formaldehyde-vapour-fixed tissue. The breakdown of VCT cells involves sequestration of glycogen from the central reserve into small cytoplasmic vesicles; subsequent release appears to be mediated by eccrine secretion. The presence of arylsulphatase activity in lysosomes within the peripheral cytoplasm of the VCT cells during the winter months indicates that glycogen breakdown may also be lysosomally mediated. The morphology of the Sertoli cells is described; during the early stages of spermatogenesis they are characterized by the presence of numerous lipid droplets which are depleted as development proceeds. Contact between Sertoli cells and developing spermatogonia is maintained by means of long septate junctions. Following spawning, the well developed lysosomal system is evident in the Sertoli cells and appears to be engaged in intracellular digestion of phagocytosed waste sperm and residual cytoplasm. Resorption of the products of gamete degeneration by the gonoduct epithelial cells is described. During regeneration, VCT cells appear to endocytose material; the ADG cells demonstrate extensive arrays of rough endoplasmic reticulum and are occasionally seen undergoing mitosis. A process involving loss of glycogen vesicles from the mantle epithelial cells by means of apocrine sections is described.