Role of ovarian follicle cells in vitellogenesis and oocyte resorption inCapitella sp. I (Polychaeta)

Capitella sp. I has a short generation time, is polytelic and produces broods of relatively large, yolky eggs at intervals of as short as 5–7 d at 20°C. The follicle cells surrounding vitellogenic oocytes in the medial portion of the ovary contain large nuclei, extensive arrays of rough endoplasmic reticulum and Golgi complexes. The coelomic surfaces of follicle cells in the outer layer are covered by blade-like microvilli, which project into the coelom. In the dorsal and lateral portions of the ovary, where mature oocytes are found, the follicle cells are covered by flat, stellate-shaped, peritoneal cells that resemble the podocytes of many invertebrate excretory organs and of the mammalian glomerulus. Changes occurring in the ovary during resorption of oocytes in the middle to advanced stages of vitellogenesis are described. Oogonia and previtellogenic oocytes are not resorbed and perhaps subsequently undergo vitellogenesis. The ovary in this highly opportunistic polychaete species may play a significant regulatory role in the control of reproduction by producing yolk precursors, regulating their uptake from the coelomic fluid via the activity of the follicle cells and by resorbing mature oocytes in response to stress.     

Ovary structure and oogenesis in Cirratulus cirratus (Polychaeta: Cirratulidae)

Oogenesis in polychaetes has, in most species, two main phases: a coelomic phase during which vitellogenesis occurs, and an ovarian phase. Details of the latter are known in very few species. Efficient reproduction requires coordination between these two phases of oocyte differentiation. The ovaries of Cirratulus cirratus (O. F. Müller) occur 2/segment throughout the fertile region of the body; 5 main stages of oocyte differentiation can be recognised on them: stem cells, oogonia, premeiotic oocytes, early oocytes and terminal oocytes. A quantitative study of the composition of the ovary throughout the reproductive cycle shows that the ovary size is approximately constant, but that the percentage of cells in the terminal oocyte stage is reduced to zero prior to spawning. This stage in oocyte differentiation is therefore a critical one, at which oogenesis may be arrested. The ovary alternates between a proliferative phase when the terminal oocytes are present, and a non-proliferative phase when they are absent. The overall rate of germ cell production for each ovary is low, less than 1 cell/ovary/day, and the, ovary tissue turnover time is greater than 2 years. A qualitative model describing the production of oocytes is presented, and the implications of the low rate of germ cell production are discussed. A low rate of germ cell proliferation, as in Cirratulus cirratus, implies that the rate of oocyte output into the coelom will be controlled by factors influencing the later stages of ovarian oocyte differentiation.     

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.     

Oocyte development in the kuruma prawn Penaeus japonicus

Female kuruma prawns (Penaeus japonicus Bate) with undeveloped, early developing, developing, nearly ripe and ripe ovaries, were collected from Ise Bay, Japan, in 1984. Oocyte development of the kuruma prawn was classified into ten stages according to morphological characters, namely: (1) synapsis stage, (2) chromatin nucleolus stage, (3) early perinucleolus stage, (4) late perinucleolus stage, (5) oil globule Stage I, (6) oil globule Stage II, (7) yolkless stage, (8) yolk granule stage, (9) prematuration stage, and (10) maturation stage. The synapsis stage is a multiplication stage. The chromatin nucleolus stage, early and late perinucleolus stages are previtellogenesis and primary growth stages. Oil globule Stage I is an initial stage of primary vitellogenesis and secondary growth. Follicle cells on the oil globule Stage I oocytes expand rapidly and reach maximum size during oogenesis. Yolk granule stage oocytes are in the initial stages of secondary vitellogenesis. Strongly acidophilic yolk granules accumulate within basophilic vesicles of the cytoplasm. The yolk granules are first concentrated in the inner part of the cytoplasm, then gradually spread to the periphery. Cortical crypts, which are separated from the oocyte cytoplasm by the cytoplasmic membrane, are situated outside of oocyte cytoplasm. Germinal vesicle breakdown (GVBD) is initiated in the late phase of prematuration and continues until the late phase of maturation immediately prior to spawning. At the beginning of the maturation stage, the oocytes are ovulated, after which the nuclei further shrink and migrate out-wards. After ovulation, meiotic division of the ovarian oocyte progressed up to the metaphase of primary maturation division. Finally, the meiotic metaphase is visible just beneath the cytoplasmic membrane in the mature oocyte. Though ovulation is synchronous within the same ovary, GVBD is not completely synchronous. Ovulated mature oocytes have many club-shaped cortical crypts in the peripheral part of the cytoplasm and contain extensive accumulations of yolk granules dispersed throughout the cytoplasm. The apical end of the club-shaped cortical crypts and cytoplasmic membrane are coated by the vitellin envelope in the mature oocyte.     

Ultrastructure of the ovary and oogenesis in the jellyfish Linuche unguiculata and Stomolophus meleagris,with a review of ovarian structure in the Scyphozoa

Ovarian structure and oogenesis has been examined in six scyphozoan species including the semaeostome Diplumularis antarctica Maas, 1908 (collected in 1987 in McMurdo Sound, Antarctic), the rhizostomes Cassiopea xamachana Bigelow, 1892 (collected in Belize in 1988), and Stomolophus meleagris L. Agassiz, 1862 (collected in Ft. Pierce Inlet in 1988), and the coronates Periphylla periphylla (Peron and Lesueur, 1810), Nausithoe atlantica Broch, 1914 (both collected in the Bahamas in 1988), and Linuche unguiculata (Schwartz, 1788) (collected in Nassau Harbor, Bahama Islands in 1989). Based on these findings and information on five other scyphozoan species from additional literature sources, at least two fundamentally different types of ovaries exist in the Scyphozoa. In semaeosotome and rhizostome species, oocytes develop in close association with specialized gastrodermal cells called trophocytes which may serve a nutritive function. However, coronate species lack trophocytes and oocytes develop freely in the mesoglea. The ovaries of S. meleagris and L. unguiculata are used as models to represent the ultrastructural events occurring during oogenesis in species having trophocytes and those lacking them, respectively. In both L. unguiculata and S. meleagris, the ovaries arise as evaginations of the gastrodermis in the floor of interradial pouches. Germ cells appear to originate from endodermally-derived gastrodermal cells and migrate into the mesoglea prior to vitellogenesis. In L. unguiculata, the oocytes develop freely within the mesoglea throughout vitellogenesis, while in S. meleagris each oocyte maintains contact with specialized gastrodermal cells called trophocytes. In the vitellogenic oocytes of both species, numerous invaginations of the oolemma result in the formation of intraooplasmic channels throughout the ooplasm. These channels are intimately associated with cisternae of rough endoplasmic reticulum and may play some role in yolk precursor uptake by substantially increasing the surface area of the oocyte. Vitellogenesis is similar in both species and involves the autosynthetic activity of the Golge complex and rough endoplasmic reticulum, and the heterosynthetic incorporation of yolk precursors through receptor-mediated endocytosis. However, in the oocytes of S. meleagris, the trophocytes probably play a role in the transfer of nutrients from the gastrovascular cavity to the oocyte. The present study suggests that scyphozoans were among the first metazoans to develop ovarian accessory cells during their reproductive evolution. The trophocyte-oocyte association observed in some scyphozoans is similar to but structurally less complex than the trophonema-oocyte association described from anthozoans. Scyphozoan ovarian morphology helps support the view that the Scyphozoa share a closer phylogenetic relationship with the Anthozoa than with the Hydrozoa.     

Effects of temperature,nutritive and metal stressors on the reproductive biology of Mytilus edulis

Experimental observations suggest that the gametogenic cycle of Mytilus edulis from Swansea Bay, South Wales (U.K.) is adversely modified by the combined effects of temperature, nutritive and sublethal metal-induced stress. During low temperature stress, oogenesis remained in the vegetative stage and vitellogenesis only commenced when temperatures were raised to ambient levels. Copper was the most toxic metal, although its uptake was slowest. A concentration of 0.05 mg l^-1 of this metal proved lethal at ambient temperatures, although at low temperatures there was no mortality. Copper suppressed both the growth of young oocytes and vitellogenesis in larger oocytes. Zinc was less toxic than copper, although this also inhibited oocyte development and resulted in severe lysis of gametes. Cadmium was the least toxic of the three metals studied and suppressed gametogenesis only in the initial stages of gonad development. The low toxicity of cadmium to gametogenesis may be a result of its high solubility and its possible storage in the digestive gland.     

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.     

中国淡水蛏卵子发生的超微结构

运用透射电镜研究中国淡水蛏Novaculina chinensis卵子发生过程中细胞和细胞器的超微结构变化,结果表明,卵原细胞的胞质含有丰富的核糖体及少量线粒体和内质网,其它细胞器不发达,卵黄合成前期,卵母细胞胞体增大,线粒体较多,量小泡装和条索状的内质网;同时随着发育的进行,出现卵黄膜、合成少量卵黄粒及产生大量脂滴,卵黄全成期卵母细胞胞体迅速增大,细胞核伸出伪足状突起;胞 内出现丰富的线粒体、溶酶体及结构独特的内质网、卵黄粒越来越多,而脂滴越来越少,成熟期卵母细胞胞体达到最大,细胞器不发达,胞质中充满大量卵黄粒,仅少量脂滴。首次观察到卵母细胞表面伸出伪足状突起,这也是外源卵黄发生的证据。讨论了中国淡水蛏卵子发生的特点.     

Utrastructural study of oogenesis and oocytic degeneration in Pecten maximus from the Bay of St. Brieuc

An ultrastructural study of oocytic development enabled the identification of changes occurring during oogenesis in Pecten maximus collected from the Bay of St. Brieuc, France, in 1987. Auxiliary cells, closely associated with developing oocytes were observed. Each oocyte seems to be associated with only one secretory cell, which is characterised by an abundant rough endoplasmic reticulum at the onset of vitellogenesis. Contact between this cell and a developing oocyte is maintained by a desmosome-like junction which can be observed when the vitelline coat is formed. These auxiliary cells seem to play a trophic role in vitellogenesis, and may be involved in the formation of the vitelline coat of the oocytes. Oocytic degeneration is discussed in detail; in this species, it is a continuous phenomenon of varying intensity throughout the year. The ultrastructural changes resulting in lysis of the oocyte are described, and the evolution of atretic oocytes is examined.     

Oogenesis and spawn-formation in the pigmy lion fish Dendrochirus brachypterus (Pteroidae)

Dendrochirus brachypterus possesses a special type of ovary in which the germinative epithelium surrounds a spongy stroma hanging in the lumen. The inner side of the ovarian wall is covered by a special type of epithelium that produces a gelatinous envelope around the gametes (spawn) during reproduction. In general, oogenesis in the lion fish resembles that of other teleosts, the characteristic difference being in the formation of ovigerous peduncles-protrusions of the spongy stroma, each of which bears a single oocyte. During oogenesis the oocytes rise above the germinal epithelium, enveloped in their follicular epithelia. The larger the oocyte the greater the length of its peduncles and the further its position from the germinal layer (Fig. 3). During this phase of development, a marked multiplication of yolk granules occurs; they increase their diameter and finally homogenize at ovulation. Under favorable thermal conditions, oogenesis continues all year round. The peduncular growth of oocytes enables the growing egg cells to move away from the egg-producing surface, thus making space available for the ovary to produce more eggs. This ability should have a survival value for these fish if we take into consideration that the most vulnerable stage in their life history is that of planktonic larvae (Fishelson, 1975).     

Spawning pattern and type of fecundity in relation to ovarian allometry in the round herring <Emphasis Type="Italic">Etrumeus teres</Emphasis>

Spawning pattern (assessed by seasonal changes in ovarian developmental stages) and type of fecundity (assessed by analysis of oocyte-size frequency distributions) of the round herring Etrumeus teres were studied in relation to ovarian growth and seasonal changes in the gonadosomatic (GSI), hepatosomatic (HSI) and liposomatic (LSI) index as well as the somatic condition of spawners (CS) in a spawning ground of southern Japan. Except for summer, mature and recently spawned ovaries occurred all year round. Oogonia and primary oocytes were present in all ovaries, and cortical alveoli stage (CA) oocytes occurred in all mature, hydrated and partially spent (PS) females (PS: females containing post-ovulatory follicles). Before hydration, a clutch of larger yolked oocytes, undergoing synchronous growth (range 0.7–1.1 mm), was present in mature ovaries which was completely separated from a more heterogeneous clutch of oogonia, primary and secondary oocytes (<0.150 mm) and oocytes in the CA stage (range 0.15–0.60 mm). As vitellogenesis progressed, the yolked clutch increased in size but the CA oocytes remained arrested. The latter entered into the secondary growth phase when hydration started in the advanced batch. Ovarian growth was isometric in all developmental stages, validating the use of GSI, which showed a consistent monthly evolution among years. Spawning stopped in summer (July and August) and peaked in winter and spring. HSI correlated positively with GSI on both a monthly mean basis (r = 0.76) and individual fish basis (liver weight explained 67–83% of the variability in ovary weight when females were grouped into 1-unit GSI intervals) suggesting a significant role of liver in vitellogenesis. LSI and CS also showed marked seasonal changes peaking from summer to middle autumn. Overall results suggest that E. teres is a multiple spawner with a group-synchronous ovarian development and indeterminate annual fecundity, with the three processes linked to an isometric growth of the ovary. We propose that such a reproductive pattern is an adaptation to produce batches of large pelagic eggs through a protracted spawning season.     

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.     

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     

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.     

Vitellogenesis in the deep-sea shark Centroscymnus coelolepis

At present, information on the reproductive physiology of Centroscymnus coelolepis, which is one of most important and widespread deep-sea shark species, is completely lacking. In this study, we investigated vitellogenesis, a key step in the reproduction biology of fishes. Specimens of C. coelolepis were collected at 2850 m depth in the Western Mediterranean Sea. The size of the collected sharks (range: 35.5-65.0 cm TL) was much lower than those typically reported for the Atlantic and Pacific Oceans. The marked distinctiveness of Mediterranean and Atlantic/Pacific populations was reflected by the achievement of sexual maturity at a smaller size in Mediterranean specimens. The examination of cytoplasmatic components of oocytes indicated that vitellogenin uptake in the ovary started when oocytes reached 14 mm in diameter. Only reproductive females displayed a significant relationship between plasmatic vitellogenin and gonadal development, suggesting that vitellogenesis in C. coelolepis is a discontinuous process. Oestradiol levels were tightly coupled with gonadal development, underlining the importance of this hormone in controlling vitellogenesis. All these findings suggest that vitellogenesis in this yolk-sac viviparous shark might occur with similar mechanisms of oviparous vertebrates.     

Vitellogenesis in the deep-sea shark Centroscymnus coelolepis

At present, information on the reproductive physiology of Centroscymnus coelolepis, which is one of most important and widespread deep-sea shark species, is completely lacking. In this study, we investigated vitellogenesis, a key step in the reproduction biology of fishes. Specimens of C. coelolepis were collected at 2850 m depth in the Western Mediterranean Sea. The size of the collected sharks (range: 35.5–65.0 cm TL) was much lower than those typically reported for the Atlantic and Pacific Oceans. The marked distinctiveness of Mediterranean and Atlantic/Pacific populations was reflected by the achievement of sexual maturity at a smaller size in Mediterranean specimens. The examination of cytoplasmatic components of oocytes indicated that vitellogenin uptake in the ovary started when oocytes reached 14 mm in diameter. Only reproductive females displayed a significant relationship between plasmatic vitellogenin and gonadal development, suggesting that vitellogenesis in C. coelolepis is a discontinuous process. Oestradiol levels were tightly coupled with gonadal development, underlining the importance of this hormone in controlling vitellogenesis. All these findings suggest that vitellogenesis in this yolk-sac viviparous shark might occur with similar mechanisms of oviparous vertebrates.     

Origin and development of the amoebocytes of Nicolea zostericola (Polychaeta: Terebellidae) with a discussion of their possible role in oogenesis

Three types of amoebocytes are present at different stages in the life history of Nicolea zostericola (Grube, 1860): a granular amoebocyte or spindle cell and 2 agranular amoebocytes, designated Type I and Type II. The agranular amoebocytes originate from specific sites on the lateral parietal peritoneum of the coelomic cavity in all the thoracic and a few abdominal segments. The origin of the granular amoebocyte is unknown. In juvenile worms the Type I amoebocyte enters the coelomic fluid and accumulates lipid and glycogen, presumably derived from reserves stored in the parietal peritoneum. Near the beginning of the vitellogenic phase of oogenesis, the Type I amoebocyte disappears and a Type II form is produced by the peritoneum. Type II cells differ cytologically from the Type I form by containing extensive rough ER (endoplasmic reticulum), Golgi complexes and free ribosomes; they appear to synthesize protein for export. At the end of vitellogenesis and near spawning, amoebocytes undergo alterations which include the migration of the nucleus to a central position, the formation of stacks and whirls of rough ER cisternae, and the appearance of vacuoles throughout the cytoplasm. It is suggested that the agranular amoebocytes obtain nutrients from food reserves stored in the parietal peritoneum and transfer them to the oocytes for use in yolk synthesis. The function of the granular amoebocytes is unknown.Contribution No.37 from the Marine Science Institute, Northeastern University, Nahant, Massachusetts, USA.Contribution No. 50, Harbor Branch Foundation, Inc.     

Growth and reproductive biology of the small penaeid shrimp Trachysalambria curvirostris in Tokyo Bay

We investigated the growth and reproductive biology of the penaeid shrimp Trachysalambria curvirostris in Tokyo Bay, Japan, by monthly bottom-trawl surveys from May 2002 to December 2004. We also examined oogenesis in T. curvirostris by histological observation of the ovary. Females grew faster and attained a larger body size for age than males. The growth rate was high in summer and low in winter and was likely to be associated with seasonal changes in water temperature. The carapace length (CL) at which 50% of females contained vitellogenic oocytes was estimated to be 17.0 mm. The reproductive season extended from May to October. Young-of-the-year appeared in October and could be traced across the months on CL histograms to the following September or October, indicating a 1-year life cycle. This extended reproductive season, together with our observation of asynchronous development of oocytes in the ovary, suggests that multiple spawning by individual females may occur during the reproductive season. Postovulated oocytes were not found among the samples we collected during the daytime, suggesting that final oocyte maturation and spawning occur at night. Cortical crypts in the cytoplasm of the oocyte, considered to be a general feature of oogenesis in penaeid shrimps, were not found in T. curvirostris, even in oocytes undergoing germinal vesicle breakdown. This result implies that the cortical reaction after spawning of T. curvirostris may be different from that of other penaeid shrimps.     

Dynamics of de novo vitellogenesis in fish with indeterminate fecundity: an application of oocyte packing density theory to European anchovy, <Emphasis Type="Italic">Engraulis encrasicolus</Emphasis>

De novo vitellogenesis is common among teleosts; however, its dynamics and the timing of batch recruitment are poorly understood. In this study, we combine a suite of methods and theories in fish reproductive biology (oocyte packing density, stereology, ovarian allometry, oocyte size frequencies and postovulatory follicle [POF] ageing) to reconstruct the steps and timing of batch recruitment in European anchovy. Using general linear modelling to standardize oocyte numbers, we demonstrate that the fractions of primary growth, cortical alveoli and vitellogenic oocytes in the ovary are relatively stable in females with migratory nucleus oocytes (MN) or with POFs 1 and 2 days old (POF-1 and POF-2), but they change abruptly at hydration. These results imply that batch recruitment in European anchovy occurs in pulses of very short duration (less than a day). The standing crop of vitellogenic oocytes in MN, POF-1 and POF-2 females equals the number of eggs contained in two mature batches.