Specific gravity and vertical distribution of sprat eggs in the Baltic Sea

During peak spawning of sprat Sprattus sprattus in the Baltic Sea in May–June egg specific gravity averaged ± s . d . 1·00858 ± 0·00116 g cm⁻³ but was significantly higher in the beginning and significantly lower towards the end of the spawning season. A close relationship was found between egg diameter and egg specific gravity ( r ² = 0·71). This relationship, however, changed during the spawning season indicating that some other factor was involved causing the decrease in specific gravity during the spawning period. The vertical egg distribution changed during the spawning season: eggs were distributed mainly in the deep layers early in the season, occurred in and above the permanent halocline during peak spawning, and above the halocline towards the end of the spawning season. Consequently, poor oxygen conditions in the deep layers and low temperatures in layers between the halocline and the developing thermocline may affect egg development. Thus, opportunities for egg development vary over the spawning season and among spawning areas, and depending on frequency of saline water inflows into the Baltic Sea and severity of winters, between years.     

Characteristics of egg and larval production in captive bluespotted gobies

Spawning of the Hawaiian coral-reef goby Asterropteryx semipunctata was diurnal, occurring at various times throughout the day. Mean length of eggs deposited in nests was 0·76 mm (range 0·67–0·84); mean egg width was 0·47 mm (range 0·41–0·52). Clutch size varied from 296 to 1552 eggs (mean=886±309), and was independent of standard length, total body weight, and body condition. Mean relative clutch size was 1·59 eggs mg^-1 total body weight (range 0·84–2·43). Clutches hatched 4–5 nights after being deposited in a nest. Mean notochord length of newly-hatched larvae was 1·88 mm (range 1·60–2·04). The minimum period of time that elapsed between egg deposition and subsequent growth of a new batch of oocytes to spawning size was 5–6 days, providing a reasonable estimate of minimum spawning interval. Compared with other gobiids, tropical species tend to have shorter incubation periods, smaller eggs and smaller larvae at hatching.     

Experimental Parameterisation of Principal Physics in Buoyancy Variations of Marine Teleost Eggs

It is generally accepted that the high buoyancy of pelagic marine eggs is due to substantial influx of water across the cell membrane just before ovulation. Here we further develop the theoretical basis by applying laboratory observations of the various components of the fertilized egg in first-principle equations for egg specific gravity (ρ_egg) followed by statistical validation. We selected Atlantic cod as a model animal due to the affluent amount of literature on this species, but also undertook additional dedicated experimental works. We found that specific gravity of yolk plus embryo is central in influencing ρ_egg and thereby the buoyancy. However, our established framework documents the effect on ρ_egg of the initial deposition of the heavy chorion material in the gonad prior to spawning. Thereafter, we describe the temporal changes in ρ_egg during incubation: Generally, the eggs showed a slight rise in ρ_egg from fertilization to mid-gastrulation followed by a gradual decrease until full development of main embryonic organs just before hatching. Ontogenetic changes in ρ_egg were significantly associated with volume and mass changes of yolk plus embryo. The initial ρ_egg at fertilization appeared significantly influenced by the chorion volume fraction which is determined by the combination of the final chorion volume of the oocyte and of the degree of swelling (hydrolyzation) prior to spawning. The outlined principles and algorithms are universal in nature and should therefore be applicable to fish eggs in general.     

A study of the population biology of Athevina boyeri Risso, 1810 in Aberthaw Lagoon, on the Bristol Channel, in South Wales

The biology of the sixth population of A. boyeri Risso, 1810 to be recorded outside of the Mediterranean basin is described. The 2 year life cycle was similar to that of other populations of the species that have been investigated. A maximum standard length of 93 mm was recorded for 2-year-old fish. Sexual maturity was attained by females at a length of 39 mm. A temporal lag in ovarian development was noted between the two spawning age groups, with the older age group spawning first. Details are provided of batch spawning in A. boyeriand the difficulties of assessing fecundity in batch spawners is discussed. Discrepancies between direct and indirect methods of assessing batch size indicated that the eggs around the largest mode may not represent the next batch to be spawned. Evidence is presented to suggest that in A. boyeri these eggs represent a ' store' from which batches of eggs are subsequently released.     

The swelling egg of the long rough dab, Hippoglossoides platessoides limandoides (Bloch)

The egg of Hippoglossoides platessoides limandoides swells when released into sea water. The swelling takes place entirely outside the ovoplasm and creates a large perivitelline space which can make up 85% of the total egg volume. Swelling occurs in both unfertilized and fertilized eggs although a small proportion of unfertilized eggs, believed not to have been activated, do not swell. Swelling is dependent upon the breakdown of cortical alveoli, together with an unusually soft and elastic chorion. The cortical alveoli, present in greater numbers than is usual in teleost eggs, release colloidal material when they break down on egg activation; adsorption of water by this material is responsible for the egg volume increase.     

Trade-off between egg mass and egg number in brown trout

Individual egg mass and fecundity increased with somatic mass in first time and repeat spawning wild anadromous and freshwater resident brown trout Salmo trutta . The egg mass was larger for similar-sized trout in south (58° N) than mid Norway (63° N), whereas fecundity was higher in mid- than in south Norway, making total gonadal investment similar in the two areas. Repeat spawners had heavier eggs than similar-sized first time spawners. The egg mass of residents was c. 10% larger than that of similar-sized first time spawning anadromous trout. Common garden experiments with offspring of wild anadromous trout showed no significant correlation between egg and somatic mass in first time spawners in two of the three populations studied. In the third population, a slight positive correlation was found. Similar results were found for repeat spawners. In the three populations, fecundity increased significantly with somatic mass in both first time and repeat spawners. Wild and hatchery-reared trout showed negative correlation between egg mass and fecundity when the effect of body size was excluded, indicating a trade-off between the two parameters. In wild trout, this was caused by variation among populations, whereas in hatchery fish, within population variation was observed in egg mass over fecundity. Furthermore, the egg mass of first time and repeat spawners were positively correlated, when adjusted for fish size. Size-specific gonadal investment was significantly higher in wild anadromous than resident trout. There was no significant difference in gonadal investment between first time and repeat spawners in wild anadromous trout. However, in the hatchery-reared trout, gonadal investment was significantly higher at repeat than first time maturation. The hatchery trout did not spawn naturally, but were artificially stripped. Among populations, a part of the variation in egg mass and fecundity is phenotypically plastic, a part appears genetically determined.     

Reproductive behavior and spawning success of female Amblyglyphidodon leucogaster (Pisces: Pomacentridae) from the Red Sea

The reproductive behavior of female whitebelly damselfish, Amblyglyphidodon leucogaster, was investigated in the Gulf of Aqaba, Red Sea over two breeding seasons. Females were promiscuous, mating with 7–10 different males throughout the season. Females lay eggs in distinct batches, defined as the total number of eggs laid in a day. Generally females deposit a batch of eggs with one male (87.2%) and are capable of laying a new batch every other day. Egg batch size averaged 4009 eggs and females laid from 2 to 22 egg batches per season. The variation in spawning success was not correlated to body size. Females preferred to deposit eggs in nests that already contained early stage eggs (0–2 days old). Within a nest, females chose to lay eggs contiguous to the youngest egg batch, regardless if the nest contained either a single batch or multiple batches of different ages. Female within-nest spawning patterns appear to be a consequence of between nest preferences for nests with young eggs. It is proposed that the strong within-nest preference is a consequence of mate selection where females may use new egg batches as a visual cue as part of a copying style. Such a style may reduce the risk of predation and increase feeding opportunities, because less time is expended in mate selection, which would provide additional resources for egg production and ultimately increase female spawning success over the breeding season. This revised version was published online in July 2006 with corrections to the Cover Date.     

The ability of Baltic cod eggs to maintain neutral buoyancy and the opportunity for survival in fluctuating conditions in the Baltic Sea

In the brackish water of the Baltic Sea successful spawning of Baltic cod Gadus morhua is restricted to the Bornholm, Gdansk and Gotland basins below the halocline, occurring at 50–80 m depth. Due to irregular mixing of the deep water, stagnant conditions occur regularly accompanied with unfavourable oxygen conditions. In avoiding stressful oxygen conditions maintenance of egg buoyancy is considered a major limiting factor for successful spawning of Baltic cod. Batches of eggs were incubated experimentally in a density gradient column. Egg specific gravity changed during development, decreasing from the time of gastrulation, then increasing prior to hatching. The changes in specific gravity varied among egg batches from different females and were related to egg quality, egg size and ambient salinity. Eggs achieve different specific gravity depending on incubation salinity. Initial egg specific gravity together with the ability of eggs to gain and maintain buoyancy up to hatching, determine larval specific gravity and the depth where hatching will occur, and thus opportunities for larval survival, avoiding stressful oxygen conditions and developing at favourable feeding conditions.     

Studies on effective PCR screening strategies for white spot syndrome virus (WSSV) detection in Penaeus monodon brooders.

We re-tested stored (frozen) DNA samples in 5 independent polymerase chain reaction (PCR) replicates and confirmed that equivocal test results from a previous study on white spot syndrome virus (WSSV) in brooders and their offspring arose because amounts of WSSV DNA in the test samples were near the sensitivity limits of the detection method. Since spawning stress may trigger WSSV replication, we also captured a fresh batch of 45 brooders for WSSV PCR testing before and after spawning. Replicates of their spawned egg batches were also WSSV PCR tested. For these 45 brooders, WSSV prevalence before spawning was 67% (15/45 1-step PCR positive, 15/45 2-step PCR positive and 15/45 2-step PCR negative). Only 27 (60%) spawned successfully. Of the successful spawners, 56% were WSSV PCR positive before spawning and 74% after. Brooders (15) that were heavily infected (i.e. 1-step PCR positive) when captured mostly died within 1 to 4 d, but 3 (20%) did manage to spawn. All their egg batch sub-samples were 1-step PCR positive and many failed to hatch. The remaining 30 shrimp were divided into a lightly infected group (21) and a 2-step PCR negative group (9) based on replicate PCR tests. The spawning rates for these 2 groups were high (81 and 78%, respectively). None of the negative spawners (7) became WSSV positive after spawning and none gave egg samples positive for WSSV. In the lightly infected group (21), 6 brooders were 2-step WSSV PCR negative and 15 were 2-step WSSV PCR positive upon capture. However, all of them were WSSV PCR positive in replicate tests and after spawning or death. Four died without spawning. The remaining 17 spawned but only 2 gave egg samples PCR negative for WSSV. The other 15 gave PCR positive egg samples, but they could be divided into 2 spawner groups: those (7) that became heavily infected (i.e. 1-step PCR positive) after spawning and those (8) that remained lightly infected (i.e. became or remained 2-step PCR positive only). Of the brooders that became heavily infected after spawning, almost all egg sample replicates (91 %) tested 2-step PCR positive. One brooder even gave heavily infected (i.e. 1-step PCR positive) egg samples. For the brooders that remained lightly infected after spawning, only 27% of the egg sample replicates were 2-step PCR positive. Based on these results, we recommend that to avoid false negatives in WSSV PCR brooder tests screening tests should be delayed until after spawning. We also recommend, with our PCR detection system, discarding all egg batches from brooders that are 1-step PCR positive after spawning. On the other hand, it may be possible with appropriate monitoring to use eggs from 2-step PCR positive brooders for production of WSSV-free or lightly infected postlarvae. These may be used to stock shrimp ponds under low-stress rearing conditions.     

Feeding behaviour of cod (Gadus morhua) in relation to spawning

The food consumption and egg production of 26 adult (13 female and 13 male) Atlantic cod ( Gadus morhua ) were monitored during prespawning, spawning and postspawning periods. Females spawned from late January to mid-April. Feeding activity occurred from December to early January and ceased for females, on average, 36 days (15–54 days) before the onset of spawning. The duration of spawning by females was, on average, 42 days (10–61 days) and feeding was suppressed by both sexes during the first three-quarters of each female's spawning period. Mature females went, on average, 70 days or 19% of the year without eating. An abrupt increase in feeding activity, particularly by females, occurred during the last quarter of spawning or shortly after the release of the last egg batch (on average, feeding started again after 91% of a female's eggs had been released or 82% of egg batches). Females consumed greater quantities of food than males during both winter and postspawning feeding periods. During spawning, females lost, on average, 29% of their body weight and males 14%. Fecundity ranged from 0.75 to 3.97 million eggs per female. The volume of eggs produced by four individual females (range = 1285–5995 ml in four to 11 batches) ranged from 99 to 195% (mean 150%) of a female's postspawning body volume. Six immature cod fed throughout the experimental period and gained, on average, 8% of initial body weight. Laboratory results were supported by stomach fullness index values of Georges Bank cod exhibiting different maturity states.     

Evaluating the use of spawning success to estimate reproductive success in a Caribbean reef fish

Observations on egg batch production by known female Stegastes partitus and the fates of those egg batches within the nests of known males revealed that spawning success was not a reliable predictor of hatching success and, hence, reproductive success because of high egg batch mortality. Moreover, while numbers of eggs per batch increased with increasing female length, both inter- and intra-individual variation in batch size was considerable, demonstrating that spawning events cannot be considered equivalent. These two findings indicate that spawning success cannot be assumed to provide a direct quantitative substitute for a measure of reproductive success in this benthic spawning reef fish.     

Aspects of the spawning of labrid and scarid fishes (Pisces: Labroidei) at Enewetak Atoll,Marshall Islands with notes on other families

Synopsis Spawning of 32 species of Labridae and 13 species of Scaridae was seen at Enewetak Atoll, Marshall Islands. Most spawned on a reef bisecting the main ocean-lagoon passage which had strong tidal currents. Others spawned on lagoon reefs and in Halimeda beds. Polygynous haremic, lek-like and promiscuous mating systems were found which were species specific. Data on reproductive patterns, sexual dichromatism, sexual dimorphism, seasonality and spawning behavior were determined. Many spawned during the day in a time-phase dependent pattern from near sunrise to sunset. Scarid spawning began at slack high water or after when currents were starting to move out of the lagoon. Labrid spawning usually started about 30 min later with some continuing up to 2 h after high tide. With high tide before sunrise, scarid spawning began 30–50 min after sunrise as the current started flowing over the reef. With high tide near sunset, spawning occurred with an incoming current. Most labroids spawned on all phases of the moon. Acanthuridae (6 spp), Caesionidae (1 sp.) and Zanclidae (1 sp.) spawned after high tide at the same time as labroids. Pomacanthidae (5 spp.) spawned only shortly before sunset without reference to tidal currents. Fishes producing pelagic eggs at the lagoon-ocean channel spawned (1) at or slightly after high tide (44spp.), (2) in late afternoon without reference to tide (6 spp.) or (3) after slack low water (1 sp. ). Spawning style can vary within a single species in different environments. Despite the presence of many piscivores, no successful predation on spawning adults was seen. Predation on newly released eggs was uncommon. Labrichthys unilineata and Anampses twistii attempted to defend their eggs for a few sec after release. Attacks by piscivores on spawning adults on tropical reefs occur once per 100–1000 spawnings. Most are wary when preparing to spawn and prespawning behavior is easily interrupted. The risk from piscivores goes down and spawning ascent speed decreases with increasing size of spawners. Egg predation by zooplanktivores is less for pair spawners than group spawners possibly due to less conspicuous gamete clouds and times of spawning. Increasing height of egg release, speed and length of the spawning ascent, and trajectory alteration of ascending adults are believed to make it more difficult for zooplanktivores to locate eggs after release. For labrids, permanent full sexual dichromatism was found among haremic, lek-like and promiscuous mating systems. Species with temporary full dichromatism, permanent and temporary partial dichromatism and monochromatism were haremic. Smaller scarids were believed to have lek-like, and larger species haremic, mating systems. Smaller scarids had male looping behavior and post spawning displays, plus faster spawning ascents and different locations for egg release than larger ones. Eggs of 21 labrids were spherical or nearly spherical, ranging from 0.55–0.80 mm in diameter, and most had one oil globule. Among 7 is scarids, 6 had spindle-shaped eggs ranging from 1.25 ×0.50 mm 2.14× 0.48 mm while one had a nearly spherical egg. One scarid egg lacked an oil globule.     

The Principles of Buoyancy in Marine Fish Eggs and Their Vertical Distributions across the World Oceans

Buoyancy acting on plankton, i.e. the difference in specific gravity between plankton and the ambient water, is a function of salinity and temperature. From specific gravity measurements of marine fish eggs salinity appears to be the only determinant of the buoyancy indicating that the thermal expansions of the fish egg and the ambient seawater are equal. We analyze the mechanisms behind thermal expansion in fish eggs in order to determine to what extent it can be justified to neglect the effects of temperature on buoyancy. Our results confirm the earlier assumptions that salinity is the basic determinant on buoyancy in marine fish eggs that, in turn, influence the vertical distributions and, consequently, the dispersal of fish eggs from the spawning areas. Fish populations have adapted accordingly by producing egg specific gravities that tune the egg buoyancy to create specific vertical distributions for each local population. A wide variety of buoyancy adaptations are found among fish populations. The ambient physical conditions at the spawning sites form a basic constraint for adaptation. In coastal regions where salinity increases with depth, and where the major fraction of the fish stocks spawns, pelagic and mesopelagic egg distributions dominate. However, in the larger part of worlds’ oceans salinity decreases with depth resulting in different egg distributions. Here, the principles of vertical distributions of fish eggs in the world oceans are presented in an overarching framework presenting the basic differences between regions, mainly coastal, where salinity increases with depth and the major part of the world oceans where salinity decreases with depth. We show that under these latter conditions, steady-state vertical distribution of mesopelagic fish eggs cannot exist as it does in most coastal regions. In fact, a critical spawning depth must exist where spawning below this depth threshold results in eggs sinking out of the water column and become lost for recruitment to the population. An example of adaptation to such conditions is Cape hake spawning above the critical layer in the Northern Benguela upwelling ecosystem. The eggs rise slowly in the onshore subsurface current below the Ekman layer, hence being advected inshore where the hatched larvae concentrate with optimal feeding conditions.     

Lunar spawning in Siganus canaliculatus

A major spawning of the seagrass rabbitfish Siganus canaliculatus occurred 4 days after the new moon in both May and June 1993, and 7 days after the new moon in 1994. The gonadosomatic index ( I _G) and serum vitellogenin (VTG) levels fluctuated according to the lunar cycle; IG and VTG levels showed peaks at around the new moon and the waning moon, respectively, suggesting that spawning of this species is synchronized with the lunar cycle. Vitellogenic oocytes appeared on day 2 after the first spawning and were fully mature on day 30. When a greater percentage of the most advanced oocytes attained the tertiary yolk stage, they formed a batch and separated from the adjacent group of smaller pre-vitellogenic oocytes, indicating that S. canaliculatus is a multiple spawner with an ovary belonging to the group-synchronous type of oocyte development. Batch fecundity, assessed using batches of oocytes at and after the tertiary yolk stage, ranged from c. 0·52 to 2·56 million eggs. The relationship between batch fecundity (F) and fork length (1) can be represented as F=0·0536854L^5·07292.     

Length rather than year‐round spawning,affects reproductive performance of RAS‐reared F‐generation pikeperch,Sander lucioperca (Linnaeus, 1758) – Insights from practice

The continuous production of large numbers of high quality gametes is essential for aquaculture, particularly in candidate species, such as pikeperch, Sander lucioperca (L.). The common practice of year‐round reproduction is under suspicion of inflicting adverse effects on the quality of the gametes through the disturbance of endogenous rhythms. We hypothesized that such perturbation does not affect RAS‐reared F‐generation broodstock. Reproductive performance (number of eggs) and gamete quality (fertilization and hatching rate) were assessed over the course of 3 years covering six independent, photothermal shifted spawning seasons in a commercial pikeperch hatchery (n = 31 egg batches of F‐generation fish in total). No substantial differences in fertilization or hatching rates could be detected between the individual spawning seasons. Fecundity varied, but there are indications for a size effect on female fecundity with intermediate sized females producing higher number of eggs (~65–70 cm). Low egg quality could be detected in batches of very large fish. In conclusion, size‐specific broodstock composition, but not year‐round reproduction of F‐generation pikeperch spawners affects the reproductive performance.     

A phylogenetic analysis of egg size,clutch size,spawning mode,adult body size,and latitude in reef fishes

Theoretical treatments of egg size in fishes suggest that constraints on reproductive output should create trade-offs between the size and number of eggs produced per spawn. For marine reef fishes, the observation of distinct reproductive care strategies (demersal guarding, egg scattering, and pelagic spawning) has additionally prompted speculation that these strategies reflect alternative fitness optima with selection on egg size differing by reproductive mode and perhaps latitude. Here, we aggregate data from 278 reef fish species and test whether clutch size, reproductive care, adult body size, and latitudinal bands (i.e., tropical, subtropical, and temperate) predict egg size, using a statistically unified framework that accounts for phylogenetic correlations among traits. We find no inverse relationship between species egg size and clutch size, but rather that egg size differs by reproductive mode (mean volume for demersal eggs = 1.22 mm³, scattered eggs = 0.18 mm³, pelagic eggs = 0.52 mm³) and that clutch size is strongly correlated with adult body size. Larger eggs were found in temperate species compared with tropical species in both demersal guarders and pelagic spawners, but this difference was not strong when accounting for phylogenetic correlations, suggesting that differences in species composition underlies regional differences in egg size. In summary, demersal guarders are generally small fishes with small clutch sizes that produce large eggs. Pelagic spawners and egg scatterers are variable in adult and clutch size. Although pelagic spawned eggs are variable in size, those of scatterers are consistently small.     

The influence of maternal length and age on the size and weight of the eggs and the relative fecundity of the haddock, Melanogrammus aeglefinus, in British waters

The diameter and dry weight of the eggs of haddock, Melanogrammus aeglefinus , are positively correlated with fish length. The correlations are largely due to the fact that many of the smaller fish that were sampled were 2 years old, and the eggs of these young haddock, which can be regarded as precocious spawners, are significantly smaller and lighter than those of older fish. The relative fecundity of 2–year–old haddock (274 eggs g⁻¹) is also lower than that of the other age classes (493 eggs g⁻¹); this has important implications for the estimation of egg production from female spawning stock biomass. It is pointed out that in some years precocious spawners represent a large component of the North Sea haddock spawning stock. When the annual egg production of this stock is calculated, it may be appropriate to apply a weighting factor to the number of eggs contributed by the 2–year–olds, on the assumption that the small eggs of these fish produce larvae that are less viable than those of older haddock.     

Spawning frequency, fecundity, egg weight and spawning type of silver pomfret, Pampus argenteus (Euphrasen) (Stromateidae), in Kuwait waters

Silver pomfret, Pampus argenteus, were collected by fishing with drift gillnets on one spawning ground in Kuwait waters during 1998–2000. Fish size frequency, sex ratio, maturation cycle, spawning frequency, fecundity and egg weight were assessed. The length–weight relationship differed between sexes whereby females were significantly bigger than males. Spawning started in mid‐May and continued until early October. During this time the water temperature ranged from 26.0 to 32.8°C, salinity was ? 39.0‰ and water depth ranged between 5 and 12 m. Large females spawned earlier than young spawners and the overall percentage of males during the spawning period was 70.3%. Spawning occurred after 13.00 h, with peak spawning between 15.00 and 18.00 hours during outgoing tide. Mean daily spawning frequency amounted to 63.2%. Spawning activity was found to be associated with the lunar cycle and spawnings were concentrated during the first and third quarters of the moon period, indicating a semilunar reproduction cycle. It was concluded that a female would spawn at least six times during the season. No change was observed in relative fecundity during the peak spawning season (June–August). Average relative batch fecundity was 176.3 eggs g^?1 somatic weight (SW), corresponding to a relative total fecundity of 1058 eggs g^?1 SW, which is 1.5 times higher than estimates obtained from counting the standing stock of oocytes. Bigger fish produced heavier eggs and the egg weight decreased as the spawning season progressed. Based on gonadal cycles, oocyte size frequency distribution and total fecundity, we concluded that silver pomfret is a multiple batch spawner with indeterminate fecundity.     

Life-history traits of invasive bighead goby Neogobius kessleri (Günther, 1861) from the middle Danube River, with a reflection on which goby species may win the competition

Life history traits of an invasive population of bighead goby Neogobius kesslerei (Günther, 1861) from the middle Danube, including absolute and relative fecundity, egg size, number of spawning batches and size at first maturation, were examined and evaluated within an epigenetic context. Ripe bighead goby females attained 42.8–142.5 mm L _S, with absolute fecundities ranging from 669 to 5646 eggs (mean 2109 eggs), and relative fecundities of 61.6–174.0 eggs g⁻¹ body weight (mean 119.6 eggs). Egg diameters varied between 0.04 mm and 1.70 mm (mean = 0.57 mm). In the pre-spawning period there was no clear size distinction in eggs (0.12–1.45 mm; mean = 0.52 mm) in 34.1% of females; whereas in 65.9% of females, two egg size groups were distinguished: group I diameters of 0.06–0.85 mm (mean = 0.43 mm), and group II diameters of 0.55–1.70 mm (mean = 1.17 mm). Females with size-group II eggs at the beginning of the reproductive season were assumed to be ready to spawn and the others to be subsequent spawners. Bighead goby appears to be altricial compared to the round goby, although in both species a shift from highly precocial towards a less precocial life history was observed. These differences, affected by epigenetic mechanisms and resulting in alternative ontogenies, may have important implications for a species' potential success in novel environments, favouring the round goby over short time periods (several years) and bighead goby over longer periods of time (decades and longer).     

Reproductive ecology of Japanese anchovy off the Pacific coast of eastern Honshu, Japan

Spawning frequency of offshore migrant populations of Japanese anchovy Engraulis japonicus ranged from 0·34 to 0·90, and was higher than that of inshore Japanese anchovy. In addition, spawning frequency of offshore populations varied in response to the sex ratio. They spawned at water temperatures of 5.0, 8.6 and 12.6° C, indicating that the minimum critical water temperature of offshore Japanese anchovy was considerably lower than that of inshore populations. A significant positive relationship was observed between water temperature and relative batch fecundity of offshore Japanese anchovy. Furthermore, water temperature was negatively related to egg size, suggesting a trade-o. between relative batch fecundity and egg size for offshore fish. At the same water temperature, relative batch fecundity of offshore populations was higher than that of inshore ones. The comparison of spawning frequency and relative batch fecundity suggests that offshore Japanese anchovy represent a reproductive ecology by which they spawn more eggs than inshore Japanese anchovy within a certain time period.