Reproductive cycle and gonadial changes in the New Zealand rock oyster Crassostrea glomerata

The annual reproductive cycle and the cyclical changes in the gonad of the New Zealand rock oyster, Crassostrea glomerata (Gould, 1850), during the breeding period of 1970–71 and 1971–72 have been described. The gonad passes through an intermediate phase, after a post‐spawning period, when sex is indeterminate. Gametogenesis begins in July and August, but follicles ripen mostly during the spring months of October and November. Maximum development is seen in November, and nearly all oysters are in spawning condition in December and January. Major spawning takes place in January or February depending upon water temperature, and spawning continues until the end of March. Larvae may be found in the‐ plankton until late in the season, to the end of April or even May. Following spawning, gonadial regression sets in, with leucocyte infiltration and phagocytosis of residual gonial cells. A greater percentage of oysters more than 1 y old are females. The majority of oysters of age 1 y and below are males.     

Reproduction in Galaxias fasciatus Gray (Salmoniformes : Galaxiidae)

A study of the reproductive cycle was made on Galaxias fasciatus Gray from streams on Banks Peninsula, South Island, New Zealand. There was no spawning migration; adults remained in the usual adult habitat to breed. The course of gonad maturation showed that spawning occurred in the autumn, from the end of April to mid‐June. Most males matured at 2 years of age and most females at 4 years old. Egg numbers in the females varied from 3800 to 23 600. Males were predominant in age groups 1–4, females in the older age groups. Amongst fish of potential breeding age there was an excess of males. Circumstantial evidence suggested that eggs were laid among piles of water‐logged debris lodged in pools and backwaters. The larvae, which are briefly described, probably hatch during floods to be swept quickly downstream to the sea.     

Measuring reproductive condition in the Greenshell™ mussel Perna canaliculus

The annual reproductive cycle of Perna canaliculus (Gmelin) was investigated for 1 year by collecting monthly gonad samples from an intertidal population. Gonads of 50 animals were dissected and photographically recorded on video before being fixed for histological sectioning. The histological gonad sections were examined both qualitatively, using a classification and scoring system (S) and quantitatively, using image analysis technology. The quantitative measures used were the proportion of: (1) sections comprising follicles (FC); (2) sections comprising gametes (GC); and (3) the proportion of follicles comprising gametes (G/F). Significant consecutive monthly changes in the qualitative and quantitative measures indicated major spawning events. Gametogenesis occurred during winter with a spawning in August‐September. Gonad condition remained low during the spring and early summer until a development period between January and March. A second major spawning event occurred between March and April. There was a high degree of synchrony in reproductive status observed between the sexes. When comparing the four measurement methods using the f statistic as an index of power the GC measure was found to be the most reliable. A gonad visual grading system was developed for rapid assessment of gonad reproductive status and tested. Visual grades of pre‐recorded gonad samples were compared to the histological measures. Increasing visual grade correlated strongly with increases in all of the histological measurements.

The visual grading was a good predictor of the spawning activity of female P. canaliculus.     

Spawning site selection,egg development,and larval drift of Galaxias postvectis and G. fasciatus in a New Zealand stream

Twelve Galaxias postvectis (shortjaw kokopu) and four G. fasciatus (banded kokopu) spawning sites were found on the margins of the Katikara Stream, Taranaki, New Zealand. This is the first time G. postvectis spawning sites have been documented. G. fasciatus spawning sites discovered in this study confirm previous observations elsewhere in New Zealand. These spawning sites were all found out of water, variable distances from the base flow water level amongst stony substrate, vegetation, and debris. Most G. fasciatus appeared to lay their eggs, and subsequently hatch, c. 3 weeks earlier than G. postvectis, which spawned from 9 to 17 May 2001. G. brevipinnis (koaro) larvae were also identified drifting downstream in late May and mid June 2001. Deposition of eggs and subsequent hatching were found to be associated with elevated flows.     

Biology of Evechinus chloroticus (echinoidea: Echinometridae) from different localities

Mean gonad indices of Evechinus chloroticus (Val.) at Kaikoura and Kaiteriteri, South Island, New Zealand, increased during the winter and spring to reach peak values during the summer and then decreased to minimum values in autumn. There was only one major summer peak at Kaikoura, but two at Kaiteriteri. The maximum mean gonad index of Kaiteriteri specimens was little higher than the minimum at Kaikoura. Absolute size of gonads and spawn producton were also lower at Kaiteriteri, perhaps because of less food there.

At both localities gametogenic cycles were correlated with gonad index cycles, progressing from unripe to ripe from late autumn to spring, but Kaikoura urchins held ripe gametes over a longer period than Kaiteriteri urchins. The volume of spawn from females was greater than that from males but males had ripe gametes (and could be artificially induced to spawn) longer. At Kaikoura, some spawning probably occurred throughout summer with a major spawning in late summer or early autumn. Large urchins with small dark gonads were found throughout the year, particularly at Kaiteriteri; these were probably senile individuals.

Although at both localities Evechinus matured at 3–4 years, Kaikoura urchins were larger at maturity.

At Kaiteriteri sex ratios of mature Evechinus did not differ significantly from 1:1, but in some populations at Kaikoura males were significantly more prevalent than females.     

Timing and habitat of koaro (Galaxias brevipinnis) spawning in streams draining MtTaranaki,New Zealand

A spawning site of Galaxias brevipinnis Giinther was located in a New Zealand stream for the first time. It was at the edge of a riffle and only partially submerged. The habitat used for spawning matched that described for G. brevipinnis in Australia. Spawning was estimated to have occurred between late April and early May and the eggs hatched in late May. The species of fish spawning was identified by rearing the eggs through to identifiable juveniles and by DNA sequencing of one individual.     

Seasonal variation in the reproductive activity and biochemical composition of the Pacific oyster (Crassostrea gigas) from the Marlborough Sounds,New Zealand

Reproductive cycles of the Pacific oyster Crassostrea gigas (Thunberg) from the Marlborough Sounds, New Zealand, were followed between June 1998 and January 2000. Histological examination of the gonad confirms an annual cycle with a winter inactive period followed by rapid gonad development and a single short spawning period. The population gonad index correlated with seawater temperature and changes in tissue dry weight, condition index, and biochemical components. In winter, few individuals with early gametogenic stages were present and rapid development of primary oocytes (diam. 11 μm) occurred during spring (September‐November). The developmental rate and the diameter of mature oocytes (37 μm) was similar for the 1998 and 1999 seasons. For a standard 110‐mm‐length oyster, maximal tissue body weight and condition index were recorded in December. Rapid weight loss in January was length dependent and was attributed to spawning. Temperature was the environmental variable which best correlated with the timing of gametogenesis. Food availability (phytoplankton biomass) may have been responsible for inter‐annual variations. The biochemical composition (% glycogen, lipid, protein) of separated gonad and somatic tissues were variable seasonally and annually. Gametogenesis (oocyte diameter) was associated with increased gonad protein and glycogen and a decrease in lipid concentrations. These changes are similar to those in Pacific oyster populations from other parts of the world.     

Size distribution of individuals in the population of Asterias amurensis(Echinodermata: Asteroidea) and its reproductive cycle in China

To obtain baseline information on the size distribution of individuals in the population and reproductive features of sea star Asterias amurensis, monthly surveys of the population were carried out from May to December 2010 and March to May 2015 in coastal waters off Yantai, China. Spawning period was predicted by gonad and pyloric caeca indices as well as anatomical and histological methods. In the A. amurensis population, both large individuals(143 mm) and small ones(42 mm) were present in all sampling months. The population size structure was driven by the appearance of big cohorts of individuals less than 55 mm from May to August. The appearance of small individuals in all months suggested a prolonged spawning period at other sites in this bay or sea stars growing slowly because of food shortage. An arm length is a good predictor to wet body weight for A.amurensis. The development of gonad was relative slow from May to September but rapidly reached a peak of20.95 in October 2010, and then dropped remarkably, indicating its spawning lasted from October to November.The same phenomenon was found from March to May 2015, suggesting another spawning during March to May,which was also verified by the results of histologic analysis on ovary. The gonad index(GI) and pyloric caeca index(PCI) tended to show a negative relationship. Due to the poor food availability, the reproductive characteristics of sea star were most likely affected by the shellfish mariculturein Yantai coastal waters.     

Ecology of New Zealand abalones,Haliotis species (Mollusca: Gastropoda)

The spawning season of Haliotis iris Martyn, as indicated by a gonad index and examination of ovaries, was late summer to autumn at Kaikoura, New Zealand, in 1967–68. In contrast, H. australis Gmelin spawned twice, once in the spring and again in the late summer to autumn. Both patterns are typical of haliotids. But in the 1968–69 year neither species spawned; full gonads with apparently ripe eggs were maintained through the winter of 1969. No reason for this inconsistency can be offered. Haliotis iris at Taylors Mistake, 154 km south, followed essentially the same pattern as Kaikoura H. iris through 1968, but spawned slightly in autumn 1969.

Haliotis iris first produces mature eggs when it is about 60 mm long and probably spawns substantially for the first time when it is 4 years old. Although fecundities of larger animals reached about 11 million eggs, not all of these were necessarily spawned. Haliotis australis also first produces mature eggs when it is about 60 mm long, but the age at which first spawning takes place could not be determined; maximum fecundity is about 3 million eggs. The sex ratios did not differ significantly from 1: 1 for either species.     

Gametogenic development and spawning of the razor clam,Zenatia acinaces in northeastern New Zealand

The potential exists for New Zealand to exploit already established markets for razor clams through development of fisheries or aquaculture industries for the New Zealand razor clam, Zenatia acinaces. However, fishery or aquaculture development for Z. acinaces requires an understanding of the reproductive cycle including the timing of gametogenic development and spawning. The reproductive cycle of Z. acinaces was studied over an 11‐month period from May 2000 to March 2001 at Kennedy Bay, Coromandel Peninsula, using qualitative standard histological analysis and quantitative measures of oocytes. Histological analysis indicated that Z. acinaces is dioecious and gametogenic development was synchronous between the sexes. Gametogenesis began in June with gametes maturing quickly and by August/September (late winter/ early spring) most razor clams were ripe. Spawning began as early as September (spring) although spawning mainly occurred during October. By December (summer), nearly all clams were completely spent. From January 2001 most clams could not be sexed as all residual gametes were resorbed. Razor clams remained in this stage during March 2001. Spawning began when the water temperature was around its lowest, c. 15°C. Monthly mean number of eggs/follicle was sensitive to changes in reproductive development, closely following patterns observed in the qualitative stagings. Patterns of monthly mean oocyte diameters did not adequately describe the spawning events observed in qualitative analyses. Sex ratios were equal over the size range (69–99 mm shell length) of clams that could be sexed. The data presented in this study provide valuable information on the timing of spawning events for Z. acinaces, necessary for developing sustainable management strategies and selecting broodstock for aquaculture.     

海湾扇贝南移后繁殖期的变动

本文根据海湾扇贝的肥满度、肉柱百分数、性腺指数及消化脓指数等指标的周年变化，并结合性腺的组织切片来确定其繁殖期。结果表明，海湾扇贝南移后的繁殖期是从每年的10月下旬开始的，直到翌年5月下旬，其中4月为繁殖盛期。繁殖期间，扇贝的性腺分批成熟，分批排放，并有消退与恢复的现象。同时，海湾扇贝引进中国北方海区并南移福建后，其繁殖规律与原产地（美国大西洋沿岸）的繁殖期有很大的不同。     

Annual gametogenesis and reproductive effort of the limpet <Emphasis Type="Italic">Cellana grata</Emphasis> (Gould, 1859) (Gastropoda: Nacellidae) in a rocky intertidal beach at Ulleungdo Island off the east coast of Korea

Widely distributed from the northern coast of Vietnam to the northern Japan, the limpet Cellana grata (Gould, 1859) occurs commonly on the south and east coasts of Korea. Despite their wide distribution range, few studies have investigated the annual gametogenesis and reproductive effort of C. grata. In an attempt to understand the reproductive physiology of the limpet, we investigated the annual gametogenesis and reproductive effort of C. grata from Ulleungdo Island off the east coast of Korea. Histology revealed that the gonial mitosis commenced in January, as the female exhibited small oogonia (10–40 μm) in the follicle. From March to June, the oocyte size increased dramatically, and fully mature eggs (110–170 μm in diameter) appeared in early summer. First spawning males and females were observed in July, as the surface seawater temperature (SST) reached 22.1°C. The spawning male and females could be observed until the end of December. Gonad somatic index (GSI), a ratio of gonad mass to the total tissue weight, of the male ranged from 0.6 (April) to 17.9 (July), while the female GSI varied from 1.0 (February) to 18.3 (July). GSI of male and female declined rapidly from July to August, suggesting that the major purse of the spawning at the study site was between July and August. Our study suggested that the commercial catch of C. grata during July and August must be suspended at Ulleungdo Island, in order to protect the spawning limpets, which enhances C. grata recruitment and the population.     

青蛤的繁殖周期

青蛤Cyclina sinensis采自福建漳浦佛昙湾。依据青蛤生殖细胞的发育规律,把生殖腺发育过程分为五期:增殖期、生长期、成熟期、排放期和休止期。青蛤怀卵量与个体体积存在线性关系:F=0.6046 0.1266V。根据青蛤肥满度、生殖腺指数和性成熟率等指标的周年变化规律,并结合性腺组织切片观察结果,认为青蛤繁殖期在9—12月,其中9月下旬至10月中旬为繁殖盛期。文中还就水温与青蛤繁殖期的关系进行了讨论。     

烟台多棘海盘车种群的个体大小分布及生殖周期

为了解烟台多棘海盘车种群个体大小分布及繁殖特征，自2010年5月至12月及2015年3月到5月，在烟台近海对该种群分别进行逐月采样调查。利用性腺指数(GI)和幽门盲囊指数(PCI)以及解剖组织学方法预测其产卵周期。结果表明：在所有的采样月份中，体长大于143mm的个体与体长小于42mm的个体在种群中均同时存在；在5-8月期间，种群结构特征以体长小于55mm的个体为主。同时该海域不同站点的采样月份中均有小个体存在，说明种群的产卵周期存在延后现象或者由于食物短缺造成了海星生长缓慢。腕长可以很好的用来衡量还行身体湿重。性腺在2010年5月-9月发育相对缓慢但在十月份迅速到达峰值20.95，之后明显下降，表明其产卵期从10月份持续至11月份。2015年3月-5月也发现了同样的现象，表明该种群自3月-5月存在另一个产卵期，且通过对卵的组织学分析也进一步证实该产卵期的存在。性腺指数和幽门盲囊指数呈负相关关系。由于食物来源短缺，烟台近海海星种群的繁殖特征极有可能受到当地近海扇贝养殖的影响。     

The life history and sexual biology of Pseudunciola obliquua (crustacea: amphipoda) in the New York Bight

Pseudunciola obliquua is the most abundant subtidal amphipod of the near-shore macrobenthos in the New York Bight south of Fire Island. It has an annual life-cycle. Breeding occurs in March and April, and a single brood of between 8 and 20 eggs per female is produced. Fecundity is linearly proportional to maternal length. The eggs take about two months to develop; the juveniles emerge in June and July. Initial recruitment in the study area was estimated to be 2980 and 5850 per m² for the 1979–1980 and 1980–1981 year classes, respectively. Of the initial recruits only about 10% survive to form the reproductive stock of the following spring.Females and males grow at similar rates and are equally abundant as juveniles and initially as adults, until they reach sexual maturity. After breeding, the abundance of males decreases rapidly due to post-reproductive death. Females continue to live, carrying the developing eggs in their brood pouches. Mean female growth increases throughout the brooding period until the young are released, shortly after which adult females also die. The entire generation of reproductive adults has died by September.     

The timing and reproductive output of the commercial sea cucumber Holothuria scabra on the Kenyan coast

The sea cucumber Holothuria scabra is a widely distributed and economically important species that has been harvested in Kenya for decades. No previous studies have been carried out on the reproduction of this species in Kenya. Standard gonad index methods were used to analyze reproductive patterns of individuals collected monthly in 1998–1999, 2000–2001 and 2006–2007. Morphological characteristics, gonad tubule lengths and fecundity were also measured. Mean monthly gonad indices were significantly correlated between males and females indicating synchronous gonad development between the sexes. Gonad indices showed a biannual pattern that was consistent in all three years with a minor spawning event occurring between August and September and a major spawning event between November and December. The pattern of gonad growth showed significant variability between years and between months. Temporal changes in gonad growth correlated significantly with gonad tubule length and absolute fecundity. Monthly gonad indices also correlated significantly with monthly measurements of air temperature and light suggesting a possible role for both factors in timing gametogenesis and spawning. There was a shift in sex ratio from unity in the 1998–1999 and 2000–2001 samples to significantly more males in the 2006–2007 samples, as well as a significant reduction in mean sizes (body wall weight) and reproductive output (gonad index) which suggests that the reproductive success of this species is potentially negatively affected by fishing.     

Buoyancy regulation by Microcystis in Lake Okaro

Seasonal changes in ovarian activity were investigated in New Zealand turbot Colistium nudipinnis (Waite 1910) and brill Colistium guntheri (Hutton 1873), collected by commercial trawlers along the west coast of the South Island of New Zealand. Both species demonstrated group synchronous oocyte development, with a capacity for multiple ovulations within a reproductive season. During a 17‐h trawl survey, ovulated turbot were caught between 1500 and 2030 h, indicating a daily spawning rhythm. The turbot and brill spawning seasons were prolonged (late autumn to mid summer). A protracted spawning season confers some advantages in aquaculture.     

Life history strategies in zooplankton communities: The significance of female gonad morphology and maturation types for the reproductive biology of marine calanoid copepods

The present review addresses the reproductive strategies of marine calanoid copepods, as affected by their physiological preconditioning, and aims to enhance understanding of their adaptations to specific environmental conditions.Knowledge about oocyte development and internal gonad structure, especially in relation to feeding conditions, is essential for a complete understanding of the reproductive strategies of the copepods. Therefore, the foci of the review are to identify general patterns in oocyte and gonad development in calanoid copepod species from marine ecosystems worldwide and to elucidate the significance of gonad structures for reproductive strategies.Oogenesis is similar in all copepod species. During maturation, the morphology of the oocytes changes distinctly and, according to oocyte size and appearance of ooplasm and nucleus, five oocyte developmental stages are distinguished. In contrast, the gonad structure and its changes during the spawning cycle differ considerably among species, and these differences are related to specific reproductive traits.Four gonad morphology types can be distinguished: the Calanus-type, found in species from all over the world with distinctly different life history traits, is apparently most common in calanoid copepods. In this gonad type, most oocyte developmental stages are present simultaneously, and usually many oocytes mature synchronously, all of which are released in one clutch. The gonad structure allows frequent spawning and large clutches, hence, high egg production rates. This may be a preconditioning for exploiting seasonally high food supply. However, the Calanus-type was also found in species producing eggs at lower rates. In the diverticula of Pseudocalanus-type gonads, only two oocyte developmental stages are present and usually fewer oocytes mature synchronously. Accordingly, the egg production rate is generally lower as compared to the Calanus-type, and apparently only this gonad-type is structurally suitable for ovigerity. Species with Pseudocalanus-type gonads are present from polar seas to the tropics, some of them being key species. The Acartia-type was scarce, found in only one species, Acartia clausi. Here all oocyte developmental stages are present, including intermediate stages, but only a few oocytes mature synchronously and are released together. High spawning frequency compensates for the small clutches, and hence egg production rate may be as high as in Calanus-type gonads. In the Aetidius-type gonad, the total number of oocytes in the diverticula is low as is the number of oocytes maturing synchronously. Less is known about the reproductive biology of species with Aetidius-type gonads; however, their distribution and feeding patterns suggest that this type is common in species inhabiting environments of low food availability.The differences in gonad structures also lead to differences in the egg size:female size ratio, as the space available for each mature oocyte depends on the total number of oocytes. Independent from gonad-type, the eggs are relatively large in species in which the gonads contain only few oocytes, whereas small eggs are produced by species with gonads filled with many oocytes. Since all species carrying their eggs in external sacs until hatching (ovigerous species) have Pseudocalanus-type gonads, the scatter in their egg size:female size ratio is low. The broadcast spawning species are of all gonad-types, and consequently the scatter among them is high.A major factor affecting the timing and magnitude of spawning of calanoid copepods is the energy supply for gonad development. Therefore, part of the review elucidates the role of internal and external resources in fuelling egg production. In many species, freshly assimilated food is transferred into egg material within a short period of time, and clutch size and spawning frequency are the two parameters that allow adjustment of egg production to food availability and temperature. However, internal body reserves may also fuel oocyte development. The extent to which oogenesis depends on ambient feeding conditions varies considerably among species and even within species, apparently reflecting their adaptation to specific environmental conditions. All copepod species continue to release eggs for a short period after the onset of starvation, indicating that a short-term nutrient pool fuels final oocyte maturation. Some species, especially from polar and subpolar regions, are capable of reproducing on internal reserves, either solely or in addition to freshly ingested food, hence, decoupling the reproduction to some extent from the spring bloom. The reproductive strategy of Calanus finmarchicus, which responds with extreme flexibility to variations in food supply, is presented here as an example for the complexity of the reproductive processes in a calanoid copepod.In accordance with their physiological pre-conditioning, the calanoid copepod species exhibit distinctly different reproductive patterns. Polar and sub-polar environments are characterized by strong seasonality in light regime, and hence, phytoplankton concentration. The reproductive activity of many dominant (herbivorous) species peaks during the spring bloom. However, species that utilize internal reserves or food resources other than phytoplankton, reproduce before and after the bloom, or even year-round. In the North Atlantic, presented here as an example for a boreal marine ecosystem, maximum reproduction of the dominant copepod species Calanus finmarchicus occurs during the spring bloom. However, the timing of peak spawning varies between areas, as the onset of the bloom varies with hydrography and climate. The subtropical Gulf of Aqaba, in contrast to other subtropical systems, is characterized by seasonal phytoplankton succession driven by thermal winter convection. These changing environmental conditions, however, did not affect the reproduction of two of the dominant species, Clausocalanus farrani and C. furcatus. In contrast, other calanoid species exhibit reproductive cycles, either related to temperature (Ctenocalanus vanus) or to ontogenetic migration (Rhincalanus nasutus).The information gained from studies of morphology and reproductive traits contributes to standardization of methods in reproductive studies. Based on detailed knowledge of gonad morphology and its changes during maturation and due to food supply, classification schemata have been developed allowing the identification of females ready to spawn. In a next step, egg production may be estimated from preserved females by assessing clutch size through the number of maturing oocytes in the gonads. This approach, however, is as yet applicable only to the species best studied, Calanus finmarchicus.The present review shows that morphological studies on gonad maturation processes may provide significant contributions to fundamental ecological questions. Thus, they extend our knowledge of reproductive ecology from simply relating reproductive traits to abiotic and biotic factors toward a mechanistic understanding of how reproduction is regulated in calanoid copepods.     

Annual pattern of brooding and settlement in a population of the flat oyster Ostrea chilensis from central New Zealand

Temporal patterns of larval brooding and settlement were investigated in a flat oyster (Ostrea chilensis) population in Tasman Bay, central New Zealand. The proportion of the population brooding larvae and larval settlement rates were monitored over 26 months. A peak period of brooding activity began in late spring and continued through summer. Maximum rates of 17% and 23% of adult oysters brooding larvae occurred in November and December, and an estimated 55–78% of adult oysters incubated larvae over the entire summer breeding period. These proportions of brooders are higher than those previously reported for Tasman Bay. A very low level of brooding activity (1%) occurred during winter. Temporal trends in larval settlement closely tracked brooding patterns. Settlement was greatest between November and January, and there were very low rates in winter. The seasonal breeding pattern in the population was intermediate between northern and southern populations, confirming a latitudinal gradient of reproductive behaviour for O. chilensis in New Zealand. Results are useful in optimising the timing of substrate deployment in an enhancement programme for the oyster fishery.     

Reproduction and recruitment patterns of the surf clam Donax serra (Bivalvia,Donacidae) on two Namibian sandy beaches

Reproduction and recruitment of the surf clam Donax serra on two Namibian beaches were studied over a period of two years. Histological examination of the gonads indicated a discontinous annual reproductive cycle, related to monthly mean sea surface temperature. The spawning season lasted from August/September to February, but juveniles (2 – 6 mm anterior-posterior shell length) were only present for three months in the intertidal zone. The condition index indicates that the species spawns during autumn and summer, but histological validation is needed. The period when juveniles are abundant is decoupled from the spawning period and therefore cannot be predicted clearly, even if the spawning period is known. Starvation, hydrodynamic processes, chemical parameters and different release times during the spawning period are thought to cause the differences in settlement time and recruitment strength between locations.