Histological investigation on the ovarian cycle of the bluefin tuna in the western and central Mediterranean

The histological analysis of eastern Atlantic bluefin tuna Thunnus thynnus ovaries caught from February to September 1999–2000, made it possible to distinguish the presence of seven oocyte developmental stages and allowed the characterization of six time-dependent ovary maturity stages. The ovaries of mature (fork length, L _F ≥ 110 cm) bluefin tuna were non-active from August (spent period) to March (quiescent period) when they contained only perinucleolar-stage oocytes. Ovary development started in April to early May (recrudescent period) with the appearance of oocytes at the lipid stage. Vitellogenesis appeared in mid-May (ripening period) and post-vitellogenesis occurred in late May to mid-June (pre-spawning period). In late June to early July, hydrated oocytes, a sign of imminent spawning, were found only in specimens caught in Balearic waters. Females ranging between 100 and 110 cm L _F, captured during the recrudescent and ripening periods, had the largest oocytes at the lipid stage, most of which were degenerating. An extensive vitellogenic atresia was observed in the ovaries of five females caught during the spawning period in non-spawning areas.     

Reproductive biology ofAwaous guamensis, an amphidromous Hawaiian goby

Synopsis Spawning season, size at first reproduction, oocyte maturation, and fecundity ofAwaous guamensis, an amphidromous Hawaiian goby, were studied from June 1989 through May 1991 in the Wainiha River, Kau'ai, Hawai'i. Female fish larger than 73 mm standard length (SL) had mature gonads from August through December in 1989 and 1990. Gonadosomatic index (GSI) values for mature females ranged from 0.2 to 14.5 during the spawning season. Male fish larger than 64 mm SL had elevated GSI values from June 1989 through December 1989 and from August 1990 through December 1990. Mature sperm were found in two male fish collected in January and February. GSI values for mature males ranged from less than 0.01 to 4.0 in the spawning season. Size-frequency distributions of measurements of vitellogenic oocyte diameters and microscopic observations of oocytes indicated this species has group-synchronous oocyte development. Ovarian maturation stages examined over a 29-month period suggest that members of the stock spawned at different times within the spawning season, although mass spawning events have been documented for this species. Estimates of clutch sizes from nests measured in situ were comparable to estimates of potential fecundity from in vitro examination of ovaries, and indicated that female fish deposited an entire clutch during a spawning event. No evidence for multiple spawning by an individual fish in a single season was found. However, microscopic observations of brown bodies in some ovaries suggested that individual fish probably spawn more than once in a lifetime.     

RNA synthesis in the ovary and oocytes of the starfish

Qualitative studies on the in vitro uptake and incorporation of tritiated uridine into RNA of the somatic and germinal elements of the starfish ovary were carried out prior to and during hormone-induced oocyte maturation and spawning.Autoradiography of nonhormone-treated ovaries indicated that the outer ovarian wall contained the highest concentration of label, with lesser amounts in the follicle cells and least in the oocytes. Oocytes and follicle cells localized at the periphery of the ovary were labeled first, and both cells became progressively labeled throughout the ovary with time; the label first appeared localized in the nucleolus of the oocyte.Sucrose gradient analysis of the separated cellular components of prelabeled hormone-treated ovaries indicated that RNA synthesis occurred in all segments of the ovary and that the spawned oocyte fraction was the least active. Synthesis of ribosomal RNA was detectable after a lag period of approximately 4 hr. Oocytes incubated in ³H-uridine during and subsequent to 1-methyladenine-induced spawning and maturation synthesized 15–19 S and low molecular weight RNA but not ribosomal RNA. Synthesis of the 15–19 S RNA was inhibited with ethidium bromide and to a limited extent by actinomycin D. Isolated mitochondrial fractions contained most of the labeled 15–19 S RNA. These data suggest the mitochondrial origin of most, if not all, of this intermediate-weight RNA. On the basis of these studies, it appears that starfish oocytes and follicle cells are metabolically active at the transitional period from growth to maturational stages in oocytes. Synthesis of RNA furthermore apparently continues in the cytoplasm subsequent to germinal vesicle breakdown and spawning.     

Reproductive features of <Emphasis Type="Italic">Upeneus margarethae</Emphasis> (Mullidae), a species recorded in the coastal zone of Vietnam for the first time

The species Upeneus margarethae described recently from the western Indian Ocean is recorded in the coastal zone of Vietnam for the first time. The reproductive features of the representatives of the species from southern Central Vietnam (Nha Trang Bay), Central Vietnam (Da Nang), and North Vietnam (Ha Long Bay) are studied. Based on the analysis of maturity stages of female’s ovaries and gonadosomatic index, the fishes spawn over the entire year in Central Vietnam, but the spawning interruption is observed in North Vietnam during a winter season. In Nha Trang Bay, 50% of females reach sexual maturity at the body length (FL) 9.8 cm. Based on histological structure of ovaries and frequency distribution of oocyte diameter before the spawning, the oogenesis is continuous. Anomalous oocyte structure is registered in 20% of the females. Egg morphology is described for 3 h after activation of ovulated oocytes. A comparison of reproductive parameters in U. margarethae and U. tragula is conducted.     

Some aspects of the reproductive biology of perch Perca fluviatilis L. A histological description of the reproductive cycle

Histological changes in the perch ovary during development are described and related to changes in gonad weight and to a macroscopic scale of maturity stages after Kesteven (1960). A single organ formed by the fusion of two primordial ovaries, a central internal oviduct, and an extremely thick chorion surrounding oocytes are characteristic features of the perch ovary. Resting oocytes can be differentiated from developing oocytes which are larger and possess a granulosa layer which permits formation of the chorion and yolk acquisition. In the maturing ovary, oocyte diameter increases rapidly and the chorion, which possesses four layers, the tunica propria, two middle zones forming a fine network, and the zona radiata, also expands. The spent ovary is disorganized with follicles and tunica wall contracted, and a number of residual oocytes may be apparent. There was no evidence of pre-ovulatory degeneration although autolysis of a small number of residual oocytes was observed. The gonadosomatic index was highest for males in September and at a maximum in females immediately prior to spawning. After spawning the index fell rapidly with lowest values recorded in June and July. Variations in the gonadosomatic index are related to developmental stages in females.     

Evidence of daily spawning in natural populations of the New Zealand snapper Pagrus auratus (Sparidae)

Synopsis New Zealand snapper, Pagrus auratus, were captured by trawling from NE New Zealand over two successive spawning seasons, and examined for acute temporal changes in gonad condition. Fish with oocytes completing final oocyte maturation predominated during the morning, with a peak in ovulated fish occurring just after midday. Afternoon catches were dominated by fish in which the most advanced oocytes had yet to begin final maturation. This suggests that ovulation is synchronised to occur soon after midday, and the high proportion (up to 100% of the catch) of fish with particular gonad stages captured at any one time indicates that daily spawning involves most of the population. Diurnal changes in oocyte diameter support a daily spawning rhythm, with numbers of large hydrated oocytes peaking in the late morning, followed by the disappearance of these oocyte stages in the afternoon. Snapper captured alive by longlining were returned to the laboratory to examine the relationship between ovulation and probable time of spawning. Unovulated fish generally ovulated close to midday on the day of capture (morning captures), or the following day (afternoon captures). The viability of ovulated eggs (proportion undergoing division after fertilization) decreased markedly after oviduct residence times of over 8 hours. This suggests that natural spawning occurs before the late evening. The results of this study are consistent with anecdotal evidence suggesting that spawning occurs every day during the late afternoon or early evening, and is similar to the reproductive patterns displayed by a number of closely related sparids. Department of Zoology, University of Otago, PO Box 56, Dunedin, New Zealand     

The multiple spawning pattern of weakfish in the Chesapeake Bay and Middle Atlantic Bight

Weakfish Cynoscion regalis were collected from commercial fisheries in the Chesapeake Bay and the Middle Atlantic Bight (n=4380) during 1989–1992 and their reproductive biology assessed using the gonadosomatic index, macroscopic gonad stages, oocyte diameter distributions, microscopic whole oocyte analysis and histology. Sex ratios were approximately 3:1, females to males, in 1990–1992. Most fish (90%) attained sexual maturity by age 1 and at a small size. Estimated mean length at first maturity was: 164mm total length (TL) for males, and 170 mm TL for females. Weakfish spawn within the Chesapeake Bay, as far north as the Virginia/ Maryland border. Although spawning occurred during May–August and gonad development and initiation of spawning was synchronous, cessation of spawning was asynchronous. There was no indication that older fish exhibited a more extended spawning season than younger fish. Weakfish are multiple spawners with indeterminate fecundity. Oocyte development is asynchronous with oocytes of all stages being present in developed ovaries. Because of the complex and dynamic weakfish ovarian cycle, typical methods of assessing reproduction, such as the GSI and macroscopic gonad stages, are inadequate for this species if not used in conjunction with more detailed methods such as histology.     

Increase in intracellular cAMP is a prerequisite signal for initiation of physiological oocyte meiotic maturation in the hydrozoan Cytaeis uchidae

In medusae of the hydrozoan Cytaeis uchidae, oocyte meiotic maturation and spawning occur as a consequence of dark-light transition. In this study, we investigated the mechanism underlying the initiation of meiotic maturation using in vitro (isolated oocytes from ovaries) and in vivo (ovarian oocytes in medusae) systems. Injection of cAMP derivatives into isolated oocytes induced meiotic maturation in a dose-dependent manner. Meiotic maturation was also achieved in isolated oocytes preloaded with caged cAMP and exposed to UV irradiation. The caged cAMP/UV irradiation-induced meiotic maturation was completely inhibited by blockers of protein kinase A (PKA), H-89, KT5720, and Rp-cAMPS. The medusae from which most parts of the umbrella were removed (umbrella-free medusae) survived for at least 2 weeks, during which time oocyte meiotic maturation and spawning occurred. When H-89 and Rp-cAMPS were injected into ovarian oocytes of umbrella-free medusae within 3 min of dark-light stimulation, meiotic maturation was inhibited or delayed. An increase in intracellular cAMP was confirmed by FlCRhR, a fluorescent cAMP indicator, in ovarian oocytes exposed to dark-light transition as well as in isolated oocytes stimulated by caged cAMP/UV irradiation. These results indicate that the cAMP/PKA signaling pathway positively contributes to light-triggered physiological oocyte meiotic maturation in Cytaeis uchidae.     

Stereological assessment of the reproductive status of female Atlantic northern bluefin tuna during migration to Mediterranean spawning grounds through the Strait of Gibraltar

The ovarian mass and gonadosomatic index (I_G) of bluefin tuna Thunnus thynnus , caught in the Strait of Gibraltar (Barbate) during migration to Mediterranean spawning grounds, were several times lower than those found in bluefin tuna from Mediterranean spawning grounds (Balearic Islands). Some of the bluefin tuna from Barbate (8.3%) were classified as immature (the most advanced oocytes present in the ovaries were early vitellogenic), and the majority (the remaining 91.6%) as non-spawning mature; the ovary contained late vitellogenic oocytes, but there was no sign of spawning activity. Stereological estimation indicated that the ovaries of spawning bluefin tuna from the Balearic Islands contained five-fold more highly yolked oocytes than bluefin tuna from Barbate. When breeding bluefin tuna cross the Strait of Gibraltar the gonad is at an incipient stage of maturation. The average batch fecundity estimated from stereological quantification of stage 4 (migratory-nucleus) oocytes in the specimens collected from Balearic was 92.8 oocytes g-1'of body mass, and the spawning frequency in this area was calculated to be 1.2 days. In specimens from Barbate a relative batch fecundity of 96.3 oocytes g -1 was estimated using stage 3 (late vitellogenic) oocyte counts.     

Reproduction mode of European Bitterling (Rhodeus amarus,Bloch, 1782) determined through rapid oocyte counts and size determination using digital imaging

This study focuses on assessing the reproduction mode of an important model species for evolutionary and behavioural ecology by using digital image analysis: the European bitterling Rhodeus amarus (Bloch, 1782). Specifications of mode of reproduction were determined using oocyte size distribution, seasonal dynamics in mean oocyte diameter and total number of oocytes in ovary samples gained from April to July 2007. The rapid oocyte count was enabled by using lucia image analysis software, which also provided measurement and colour estimations of oocytes. Bitterling ovaries showed features typical for indeterminate spawners, i.e. a continuous distribution of oocyte size over the reproductive season and recruitment of new pre‐vitelogenic oocytes in the second half of the reproductive season. These results are consistent with the view that the European bitterling is a batch spawning fish with indeterminate fecundity.     

Apparent semi-lunar spawning rhythmicity in a brackish cardinalfish

The purpose of the present study was to examine the lunar-related spawning rhythmicity of the amboina cardinalfish Apogon amboinensis, which is a euryhaline species inhabiting mangrove creeks in the Indo-Pacific area. During the reproductive season, the gonado-somatic index increased towards and peaked within a week of the first and last quarter moon. Histological observations of the ovaries also showed development of yolk-laden oocytes towards the first and last quarter moon; postovulatory follicles, an indicator of spawning, appeared around these lunar phases. Fish with immature oocytes in the ovary were also collected in the same lunar phases, suggesting that at least two fish populations with different oocyte development stages exist at any given time. The levels of two steroid hormones secreted from the ovarian pieces into a culture medium with human chorionic gonadotropin were measured using enzyme-linked immunosorbent assay (ELISA). The level of oestradiol-17β increased around the new and full moon periods. On the other hand, 17α,20β-dihydroxy-4-pregnen-3-one levels increased around the first and last quarter moon, suggesting that the fish are actively undergoing vitellogenesis and final oocyte maturation around the respective lunar phase. These results suggest that with the 1 month ovarian development process, A . amboinensis exhibits a semi-lunar spawning pattern with peaks around the first and last quarter moon. When A . amboinensis were reared under laboratory conditions without the tidal stimuli, mouth-brooding was initiated in 13 of 20 males within a week of the first and last quarter moon. The possibility of a lunar-related endogenous rhythm in A . amboinensis is discussed.     

In vitro inhibition of oocyte and follicular maturation and spawning in starfish (Asterias forbesi) by 2-4-dinitrophenol

The in vitro effects of 2-4-dinitrophenol (DNP) on spawning and follicular and oocyte maturation in starfish ovaries and its various cellular components were investigated. Spawning and oocyte and follicular maturation induced by starfish gonadotropin radial nerve factor (RNF) in isolated ovarian fragments were all inhibited by appropriate doses of DNP. DNP inhibits processes which occur shortly after addition of the gonadotropin; in ovarian fragments insensitivity to DNP inhibition occurred shortly after addition of RNF but prior to initiation of spawning. Spontaneous follicular and oocyte maturation which occurred following release of ovarian follicles into sea water was prevented by DNP. In non-spontaneously maturing follicles released from the ovary, DNP inhibited both follicle and oocyte maturation induced by the secondary stimulator of spawning and maturation, 1-methyladenine (1-MA). DNP also inhibited 1-MA induced meiotic maturation in isolated immature oocytes incubated in the absence of follicle cells. Inhibition of oocyte maturation was not associated with inhibition of 3H-1-MA incorporation by isolated oocytes. Immature oocytes incubated in the presence of DNP underwent maturation following washing and subsequent exposure to 1-MA. Immature oocytes initially exposed to both 1-MA and DNP, however, showed decreased maturation responsiveness following washing and re-exposure to 1-MA. The results suggest that the inhibitory effects of DNP on spawning and oocyte maturation are the result of direct effects on the oocytes and possibly other cells and tissues within the ovary.     

Maturation and spawning processes of anadromous and resident pond smelt in lake ogawara

Pond smelt,Hypomesus nipponensis McAllister, in Lake Ogawara demonstrate alternative life history strategies, as evidenced by the coexistence of anadromous and resident fish. However, it is unknown if anadromous and resident groups interbreed. In this study, maturation and spawning processes were examined and compared between anadromous and resident groups. Histological observations indicated negligible variation in the maturational stage composition of oocytes, the frequency of oocyte diameter being unimodal for all specimens at different maturational stages. Oocytes were absent in the ovaries of spent fish. Accordingly, the species can be considered a semelparous spawner with unimodal oocyte diameter distribution. Temporal changes in the proportion of spent fish were compared between anadromous and resident groups. Spawning of both groups began in late March and peaked over April 8–12. Although both groups did not differ significantly in the period of peak spawning, anadromous fish finished spawning earlier than resident ones. Anadromous fish were not able to spawn upon migration into Lake Ogawara, and quickly matured after immigration, contrasting with resident fish.     

Ovary of the golden crab,Chaceon fenneri: I. Post-spawning and oosorption

Oosorption has been considered an important strategy in many invertebrate species which occurs in response to behavioral, ecological, or physiological factors. In crustaceans, the early light microscopic studies of the ovary attributed a role in oosorption to follicle cells, hemocytes, or phagocytes. In this study, ovaries were collected from female golden crabs following spawning and processed for examination by electron microscopy. Following spawning, several unspawned oocytes which had become dissociated from their follicle cells were found in the ovaries. They appeared to be lodged within the lumen. Such oocytes were observed undergoing various stages of autolysis. At no time were hemocytes or recognizable phagocytes found in the lumen of the ovaries or in contact with the degenerating oocytes. Follicle cells which had surrounded the oocytes prior to the time of spawning exhibited disrupted membranes. Resorption of unspawned eggs appears to occur by autolysis of the individual oocytes. Several of the females who had recently spawned had numerous sperm in their ovaries. Such sperm may have been pressed into the lumen at the time of spawning or during the fixation process.     

In vitro Inhibition of Oocyte and Follicular Maturation and Spawning in Starfish (Asterias forbesi) by 2-4-Dinitrophenol

The in vitro effects of 2-4-dinitrophenol (DNP) on spawning and follicular and oocyte maturation in starfish ovaries and its various cellular components were investigated. Spawning and oocyte and follicular maturation induced by starfish gonadotropin radial nerve factor (RNF) in isolated ovarian fragments were all inhibited by appropriate doses of DNP. DNP inhibits processes which occur shortly after addition of the gonadotropin; in ovarian fragments insensitivity to DNP inhibition occurred shortly after addition of RNF but prior to initiation of spawning. Spontaneous follicular and oocyte maturation which occurred following release of ovarian follicles into sea water was prevented by DNP. In non-spontaneously maturing follicles released from the ovary, DNP inhibited both follicle and oocyte maturation induced by the secondary stimulator of spawning and maturation, 1-methyladenine (1-MA). DNP also inhibited 1-MA induced meiotic maturation in isolated immature oocytes incubated in the absence of follicle cells. Inhibition of oocyte maturation was not associated with inhibition of ³H-1-MA incorporation by isolated oocytes. Immature oocytes incubated in the presence of DNP underwent maturation following washing and subsequent exposure to 1-MA. Immature oocytes initially exposed to both 1-MA and DNP, however, showed decreased maturation responsiveness following washing and re-exposure to 1-MA. The results suggest that the inhibitory effects of DNP on spawning and oocyte maturation are the result of direct effects on the oocytes and possibly other cells and tissues within the ovary.     

Comparative morphology and histology of the ovaries of the spined loach Cobitis taenia L. and natural allopolyploids of Cobitis (Cobitidae)

The maturity of ovaries, gonado-somatic index and size of oocytes in particular developmental stages during the reproductive period of spined loach Cobitis taenia and allotriploid and allotetraploid Cobitis were examined. The ploidy levels of all the loaches were determined according to karyotypes. All the investigated females spawned multiple times and the spawning period was from the end of May (water temperature c. 18·5° C) to mid- or the end of July. Some of the triploids had a longer spawning period which lasted until the end of August. Each female could lay several portions of eggs which differed in size and number during the spawning season. The relative proportion of oocytes of each stage in the ovaries during the reproductive period changed. The sizes of oocytes at the particular stages of triploids were statistically significantly larger than oocytes in the respective stages in C. taenia (diploid). The sizes of the oocytes (each stage) of C. taenia from both populations were not significantly different.     

Comparative study of reproductive biology in single- and multiple-spawner cyprinid fish. I. Morphological and histological features

To clarify the dynamics and regulation of oogenesis in single- and multiple-spawning cyprinid fish with group-synchronous oocyte development, a multidisciplinary approach to their reproduction was undertaken using three species from the River Meuse (Belgium): the roach Rutilus rutilus as a single spawner, and the bleak Alburnus alburnus and the white bream Blicca bjoerkna as multiple spawners. The gonadosomatic index (GSI) and histomorphometric changes (distribution of oocyte size, relative proportion of the various oocyte stages) in the ovary are compared. Different patterns of GSI and oocyte growth were observed both between the single- and multiple-spawner fish and between the two multiple spawners. Maximum GSIs were higher in roach (21%) than in bleak and white bream (17.7 and 14.5%, respectively), and compared to the rapid decline of GSI in the roach population, the GSI of multiple spawners decreased progressively during the spawning season. In roach, a short gonadal quiescent period and an early onset of vitellogenesis was recorded from late summer onwards whereas, in bleak and white bream, exogenous vitellogenesis was not systematically observed before winter. A protracted spawning season and/or a low water temperature in autumn are hypothesized to explain this long period of gonadal quiescence. In bleak, during the spawning season, the oocytes recruited arose from the stock of endogenous vitellogenesis and attained the final maturation stage very rapidly. This recruitment occurred during the whole spawning season. In white bream, the differentiation of vitellogenic oocytes from smaller oocytes was completed before the onset of the spawning season. During the spawning period, the proportion of vitellogenic oocytes decreased progressively whereas the percentage of oocytes in the final maturation stage remained approximately constant.     

The effect of oocytic atresia on fecundity estimates of the rabbit fishSiganus sutor (Pisces: Siganidae) of Kenyan marine inshore waters

In the strongly group-synchronized oocyte development ofSiganus sutor (Valenciennes, 1835) the group of oocytes to be released in the following spawning, is identified. The smallest size of oocyte belonging to this group was identified by the presence of cytoplasmic vacuoles in oocytes in histological sections. These vacuolated oocytes corresponded to oocytes of 150 µm diameter obtained by treatment with Gilson's fixative. The mean number of such oocytes in stage 4 (late developing) ovaries was found to be 638 000. The proportion of these oocytes removed by atresia before spawning was determined on histological sections to be 5%. The corrected estimate of mean fecundity was thus 606 000 oocytes per spawning.     

Preliminary results of the in vivo studies on ovarian resorption in carp (Cyprinus carpio L.)

Oocyte resorption in the ovaries of sexually mature carp, which did not spawn, was investigated using a method of sampling ovaries in vivo . A 2-year study revealed that a portion of the oocytes had undergone a slow resorption while the basic mass of the ovaries, throughout the experiment, consisted of the oocytes similar to those of stage IV of sexual maturity. At the same time no growth of the oocytes of the earlier maturation stages was found. The condition of the ovaries in the females studied indicated their complete infertility, at least for three successive spawning periods.     

Role of the tidal cycle in the gonadal development and spawning of the tropical wrasse Halichoeres trimaculatus

Many wrasses on coral reefs exhibit daily spawning that peaks around daytime high tides. In this study, we examined tidal-related ovarian development in the threespot wrasse, Halichoeres trimaculatus, a species common on coral reefs in the Indo-Pacific Ocean. When the fish were collected in the morning at different tidal phases, the gonadosomatic index (GSI) and ovarian histology changed; concomitant with increases in GSI towards high tide, a clutch of the most advanced oocytes developed from vitellogenic to maturation stages. Ovulated eggs and post-ovulated follicles (POF) existed in most ovaries around high tide, but only POF remained around ebb tide, suggesting that spawning occurred during or after high tide. We noticed that tidal-related spawning was considerable in the morning and that most ovaries collected on the afternoon high tide exhibited post-spawning features. This suggests that certain labrid species possess plasticity with regard to their spawning time and utilize potent environmental cues to ensure their reproductive success. When pieces of ovary were incubated with precursor steroids, high conversion of testosterone to 17beta-estradiol occurred during high and ebb tides, while that of 17alpha-hydroxyprogesterone to 17alpha,20beta-dihydroxy-4-pregnen-3-one and 17alpha,20beta,21-trihydroxy-4-pregnen-3-one was observed during low and flood tides. Incubation of pieces of ovary with human chorionic gonadotropin resulted in similar fluctuations in the steroid hormones with tidal phase. Production of these steroid hormones correlated with oocyte development in the ovaries and was probably regulated by gonadotropin. These results demonstrate that the daily cycle is fundamental for oocyte development, and that the tidal cycle is superimposed on this process.