Reproduction and condition of female Octopus mimus (Mollusca: Cephalopoda)

The relationship between reproduction and condition was studied in a 15 mo sample of 919 maturing, mature and post-spawning female Octopus mimus (388 to 3714 g) caught in Iquique (North Chile). O. mimus is a semelparous species, with reproduction taking place all year round. Investment in reproductive tissues was, on average, 9.9% of mature female body weight, independent of season. However, somatic growth during maturation was dependent on season and varied between 26 and 63% of the whole-body growth in weight. The condition of females did not vary markedly until spawning, although seasonal variations were apparent, winter being the most unfavourable. Condition deteriorated dramatically after spawning, during parental care of the eggs. During this period, somatic-tissue depletion, mainly from the muscles, was >25% of the total body weight of mature females. The fecundity of O. mimus was probably limited by the costs associated with parental care of the eggs.     

Size-related reproductive biology of the infaunal bivalve<Emphasis Type="Italic"> Abra alba</Emphasis> (Bivalvia) in Kinsale Harbour (south coast of Ireland)

The reproductive behaviour of 248 specimens comprising four size classes of the infaunal bivalve Abra alba (Wood) was investigated between September 1994 and November 1995 in Kinsale Harbour. Small males returned a very small proportion of sexually mature and spawning animals. By contrast, no spawning females were found in this size class, suggesting that males develop and mature at a smaller size than females. Mean gonad maturity indices indicated that, except for the smallest size class, A. alba exhibits two spawning events in 1 year, i.e. a lesser spring and a major autumn spawning event. The spring event was well synchronised between males and females, while the autumn spawning was more broadly synchronised between the sexes. Only one spawning event was recorded for very large males and females, also occurring in spring. Spawning stages were recorded for both sexes over all size classes between February and November, indicating only a short period of sexual repose, if any. Oocyte diameters did not show a discrete size range from developing to spawning stages. All stages were seen to contain varying proportions of smaller, less mature oocytes, suggesting that large A. alba females do not develop and spawn en bloc, but release their gametes periodically. Maturity indices showed only a broad similarity with off-bottom temperatures.Communicated by O. Kinne, Oldendorf/Luhe     

Plasma sex steroid and vitellogenin profiles during gonad development in wild Mediterranean amberjack (<Emphasis Type="Italic">Seriola dumerilii</Emphasis>)

Mediterranean amberjacks, Seriola dumerilii Risso, were caught off the Pelagie Islands, in the south Mediterranean Sea, between May 1997 and June 1999. Fish blood was sampled, and gonads were collected at 10-day intervals throughout the spawning period and at monthly intervals during the resting period. Concentrations of plasma estradiol-17ß (E₂), testosterone (T), 17,20ß-dihydroxy-4-pregnen-3-one (DHP) and vitellogenin (Vtg) in females; and plasma T and 11-ketoT (11-KT) in males were correlated with changes in gonadal development. The first females that had already ovulated (F5) were found in late May. Most mature females (F4) were caught in June. Post-spawned females (F6) were found from late July until September. Estradiol-17ß was at baseline levels (<0.02 ng ml^–1) during autumn/winter and rapidly peaked (6.29±0.68 ng ml^–1) from May to early July. Plasma T levels showed a similar profile and were positively correlated to E₂ (r²=0.668) during the spawning period. Continuously elevated levels of E₂ and T were observed during the spawning season in vitellogenic females (stages F3, F4 and F5). Resting females were found during the autumn/winter months. Vitellogenin levels increased during May and peaked in June, reverting to undetectable levels in August, in parallel with sex steroid changes. Plasma DHP levels peaked in June (283.45±97.3 pg ml^–1), falling to basal values (<5 pg ml^–1) in August. DHP levels were higher in mature females (F4) than in maturing (F3) and in partially ovulated (F5) females. DHP values increased during germinal vesicle migration, peaked during germinal vesicle breakdown and decreased again during complete oocyte hydration. In males, changes in T and 11-KT plasma levels were related to testis development. The highest levels of T (5.76±2.64 ng ml^–1) were measured during spermatogenesis and highest 11-KT (5.28±3.6 ng ml^–1) in males with milt, from May to June. This study provides information, for the first time, on the relation between plasma sex steroid profiles and gonad development in wild Mediterranean amberjack, a useful benchmark for broodstock monitoring under controlled conditions.Communicated by R. Cattaneo-Vietti, Genova     

Multiple spawning in the tropical squid Photololigo sp.: what is the cost in somatic growth?

This study assesses the potential of the tropical loliginid squid Photololigo sp. to lay multiple batches of eggs and examines changes in somatic growth during reproduction. Histological analysis of the ovary and the relative size of the oviduct to mantle weight and ovary weight were used to determine the potential for multiple spawning. Ovaries of mature females always had immature and mature oocytes present, suggesting that not all the oocytes were maturing simultaneously and that multiple batches of eggs were being produced. Furthermore, poor correlations of oviduct weight with body size and ovary weight indicated that mature oocytes were not accumulating in the oviduct for a single spawning event. Both these observations supported the hypothesis that Photololigo sp. has the potential to lay multiple batches of eggs throughout its life. Specific growth rates, length-weight relationships, relative growth of somatic and reproductive tissue and microscopic assessment of muscle tissue were compared between immature and mature females. Growth rates of immature females were almost twice as fast as those of mature females. Mature females also had no large muscle fibres present, suggesting that energy for reproduction was mobilised from the muscle tissue.     

Reproduction and annual gametogenic cycle in Nephtys hombergii and N. caeca (Polychaeta: Nephtyidae)

The gametogenic cycles of Nephtys hombergii Audouin et M. Edw. and N. caeca Fabricius are described. Both species are polytelic (=discrete, iteroparous) and breed in their second and subsequent years. They spawn in May in the Tyne estuary. After spawning, N. hombergii retains a large number of gametocytes, which are ultimately resorbed. A new generation of gametocytes is proliferated by September and mature gametes accumulate during the winter months. Gametic development is not well synchronised.     

Reproductive biology of the spiny lobster, <Emphasis Type="Italic">Panulirus Penicillatus</Emphasis>, in the southeastern coastal waters off Taiwan

The reproductive biology of spiny lobster, Panulirus penicillatus, was studied based on 2,068 lobsters, ranging from 34.28 to 131.60 mm carapace length (CL), sampled in Taitung coastal waters from September 2003 to December 2004. The overall sex ratio approximated 1:1 (χ² = 0.02, P > 0.05), but the monthly sex ratios in 2004 showed significant differences and males were predominant in sizes larger than 80 mm CL. Reproductive activity, assessed using histology, a gonadosomatic index and percentage of ovigerous females, indicated that the mature females could be found in every month and that the major spawning occurred from May to September. The presence of re-developing/re-ripe ovaries by month and size-specific spawning time suggest that larger mature females (>60 mm CL) spawn at least three times a year while smaller new mature females spawn at least once a year. For females, the estimated sizes at 50% physiological and functional maturity were (mean ± SE) 56.46 ± 0.56 mm CL and 66.63 ± 1.07 mm CL. The estimated sizes at functional maturity were between 72 and 74 mm CL for males. The number of eggs per spawning event (brood size, BS) was related to CL by the equation Y _BS = 2.4 × 10^-3CL^4.18 (r ² = 0.902, n = 12). Female lobsters with CL ranging from 60 to 80 mm made the greatest contributions to egg production because of their high brood size and active reproductive activity. A minimum legal size should be established for the fishery to protect egg production potential of lobster population in the southeastern coastal waters off Taiwan.     

Reproduction of<Emphasis Type="Italic"> Ophiactis resiliens</Emphasis> (Echinodermata: Ophiuroidea) in New South Wales with observations on recruitment

Reproduction of the ophiuroid Ophiactis resiliens Lyman 1879, a common species in the shallow waters around Australia, was examined over 1 year in two populations near Sydney, New South Wales. Gametogenesis was documented by histological examination of the gonads. Vitellogenesis in females and spermatocyte proliferation in males started in February and March. O. resiliens had an annual spawning period from May to September/October with peak gamete release from May to July. Thereafter, spawning occurred in some specimens through November. Gravid gonads were present for approximately 2 months longer in O. resiliens from Clovelly Bay than in those from Little Bay. At both sites spawning was episodic and gametogenesis continued through most of the spawning season. Most specimens (50–100%) collected from November to March had indeterminate/recovery stage gonads, the sex of which, could not be determined. The timing of gametogenic renewal during these months varied among individuals. O. resiliens has a 3-month planktonic stage and the presence of juveniles, 0.5 –1.5 mm disk diameter, in the coralline algal turf at Little Bay from February to May, suggests that settlement occurs in summer and autumn at this site. In contrast, juveniles were rarely encountered in coralline turf at Clovelly.     

Reproductive cycle of<Emphasis Type="Italic"> Bispira volutacornis</Emphasis> (Polychaeta: Sabellidae) on the west coast of Ireland

The reproductive cycle of Bispira volutacornis, a dioecious polychaete, was followed over two spawning periods in Lettercallow Bay, on the west coast of Ireland. In the younger generation of sexually mature adults, gender can be determined on the basis of colour, the dorsal aspect of the males being cream at maturation, whilst the females are pink at the previtellogenic stage and an olive green at maturation. An annual reproductive cycle of 12 months shows that oocyte/sperm maturation is extraovarian. The male reproductive cycle proceeded at a more rapid pace than that of the female cycle, with sperm maturing earlier. Spawning in B. volutacornis occurred between late July and early September. B. volutacornis is a polytelic species, surviving spawning and releasing all gametes in a single batch, with a mean spawned oocyte diameter of 118 m. The reproductive cycle appears to be regulated by a seasonal change in water temperature, and spawning is timed to produce larvae during the autumnal planktonic bloom in Lettercallow Bay.Communicated by J.P. Thorpe, Port Erin     

Reproductive cycle of the endemic cassiduloid<Emphasis Type="Italic"> Cassidulus mitis</Emphasis> (Echinoidea: Cassiduloida) on the Brazilian coast

Cassidulus mitis Krau, 1954 is an endemic species from Rio de Janeiro, Brazil. To study the reproductive cycle of this species, samples were collected at Praia Vermelha, in Guanabara Bay, from October 1998 to April 2000. The sex ratio for C. mitis was 1:1, and reproduction occurred throughout the year. The gonadal index of males was greater than that of females. Five gametogenic stages were identified in males: early growth, premature, mature, partially spawned and early growth with a partially spawned stage. There were no spent or recovery stages such as those seen in females. Females had six gametogenic stages: recovery, early growth, premature, mature, partially spawned and spent stage; there was no early growth with a partially spawned stage as there was in males. The mean oocyte diameter was 382 m (SD=49 m), and the mean number of juveniles per female was 100 individuals (SD=108). The anterior gonads were frequently smaller than the posterior ones, and there were differences in the gametogenic stages between the anterior and posterior gonads. First sexual maturation occurred in individuals with a diameter of 17 mm. The intestinal wet weight was two- to threefold higher than the test wet weight. This may indicate that C. mitis uses its intestine as a weight belt to avoid displacement from the substratum.Communicated by P.W. Sammarco, Chauvin     

Seasonal migrations of plaice (Pleuronectes platessa) through the Dover Strait

Analysis of paired-haul mid-water trawling experiments conducted in the five months November to March during the years 1985 and 1988 revealed the seasonal pattern of migration of plaice (Pleuronectes platessa L.) moving through the Dover Strait between the Southern Bight of the North Sea and the English Channel. Mid-water catches of maturing fish were highest on south-going tidesprior to peak spawning (late January), while catches of spent fish, were highest on north-going tidesafter peak spawning. Detailed analysis of the catch data provided evidence that males complete their pre-spawning migration earlier, and their post-spawning migration later, than female fish and consequently spend more time on the spawning ground. Catches of immature female fish indicated a migration south following that of the mature fish. This dummy run may be a method by which immature plaice use the presence of high densities of mature and spawning fish to learn the location of the spawning ground. The analysis also indicated that differences in catch rates between day and night are unlikely to be the result of gear avoidance by day. The results confirm that selective tidal-stream transport is a key migratory mechanism for plaice in areas of fast tidal streams on the European continental shelf.     

Reproduction of the Antarctic fish Nototheniops nudifrons

The reproductive biology of the Antarctic fish Nototheniops nudifrons (Lönnberg, 1905) was analyzed by examination of the gonads of fish collected in March and April 1985 in trawls near Low Island, Antarctic Peninsula, and compared to direct observations of reproduction and early larval development in the laboratory from March to October of the same year. Males and females reached sexual maturity at an age of 4 to 5 yr. Mature males differed in coloration from females and immature males. Ovaries of sexually mature females contained two distinct size modes of vitellogenic oocytes, representing two separate clutches of developing eggs. Females spawned 100 to 3 500 demersal eggs, which were laid in a nest in crevices or under rocks, and guarded by the male for about 4 mo. Females did not assist in nest defense or egg care. Most spawning in the field and in the laboratory occurred in late fall and early winter (May to June). A second clutch may be spawned in spring (November and December). Eggs hatched after 124 d, and larvae were raised for 38 d. Otoliths of larvae contain internal microincrements, which are deposited in a daily fashion, and are visible by light microscopy. The otoliths of 32 adult fish were examined by scanning electron microscope, and counts of microincrements in these otoliths allowed the backcalculation of hatching dates. Estimated hatching dates were between September and May.     

Reproductive biology of the lanternfish Benthosema pterotum from the Indian Ocean

Samples of Benthosema pterotum (Alcock) were obtained from the Arabian Sea (1976, 1979, 1981, 1983, 1984), off Mozambique (1978) and from the Bay of Bengal (1979). The sexual maturity stages are described. For females, the size of the largest oocytes was found to be most useful for size of the largest oocytes was found to be most useful for assessing maturity. Mature and spawning fish were found in all seasons. Samples from November 1983 differed from all others in having very few mature females. A few apparently spent fish were observed in July to August 1979 and November 1983. Some females mature at 25 mm and males at 20 mm, whereas others can still be immature at 45 and 40 mm, respectively. Of the total number of stations, four had significantly more males than females, twelve significantly more females, and forty-seven displayed no difference in the sex ratios. The vertical migration of the mature and spawning fish did not differ significantly from that of other individuals. Batch fecundity ranged from ca. 200 to 3 000 eggs fish ranging from 27 to 52 mm, relative fecundity from ca. 2 000 to 7 000 eggs g^-1 maternal dry weight. There are indications that B. pterotum spawns only once, but no firm conclusions could be drawn.     

Maturation,fecundity, and spawning strategy of the thornback ray, <Emphasis Type="Italic">Raja clavata</Emphasis>: do reproductive characteristics vary regionally?

In Portuguese waters, thornback ray Raja clavata spawns mainly between May and January, although females and males in spawning condition are found throughout the year. The maturation process can be divided into three main phases by using information on gonad weight, oviducal gland and uterus width in females and on gonad weight, clasper length and sperm duct width in males. Females attain length-at-first-maturity at 784 mm and males at 676 mm, at ages of 7.5 and 5.8 years, respectively. In females larger than length-at-first-maturity, a resting stage was identified characterized by low gonadosomatic index and well-developed oviducal glands and uteri. These results along with the low proportion of adult females that are effectively reproducing per month demonstrated that the thornback ray cannot be considered a continuous spawner as described in other studies. Fecundity was determinate with about 35 eggs released per batch. During the spawning season, a total of four batch episodes occur indicating that the total fecundity was approximately 136 eggs per female. Regional differences may exist in the reproductive strategy of the species, namely on the duration of the spawning season, length-at-first-maturity, and fecundity, which can be related to a more intense fishing pressure in northern European waters.     

The Arctic sea butterfly<Emphasis Type="Italic"> Limacina helicina</Emphasis>: lipids and life strategy

The sea butterfly Limacina helicina was collected from May to September 2001 in Kongsfjorden, Spitsbergen, to investigate population structure and body and lipid composition with regard to life cycle and reproductive strategy. Veligers and juveniles were only found in late autumn and spring, whereas females occurred from July to September. The size of the females increased until mid-August and decreased in September. Dry and lipid mass were closely related to size; dry mass increased exponentially and lipids linearly with size. The lipid content was highest in veligers (31.5% of dry mass) and juveniles (23.6%) but low in females (<10%). Phospholipids were the dominating lipid class followed by triacylglycerols. Females, veligers, and egg ribbons, all from September, were richest in phospholipids. Juveniles contained the highest amounts of triacylglycerols, whereas females had low levels in July and the beginning of August. In mid-August, levels of triacylglycerols were variable and higher. This suggests that females were in their main spawning period and the high variability in triacylglycerols points to different stages within the spawning cycle. Enhanced amounts of free fatty acids in females from July may be related to gonad development. The 16:1(n-7) fatty acid was more dominant in spring whereas 18:4(n-3) increased in summer and autumn, which reflects a change in diet from diatom-dominated food items in spring to dinoflagellates in summer/autumn. Small amounts of long-chain monounsaturated fatty acids suggest ingestion of copepods, and the fatty acid composition of veligers feeding on particulate matter. L. helicina has a one-year life cycle with peak spawning in August and over-winters as veligers that may grow to juveniles during the winter period. They metamorphose into juveniles during spring, develop to males in early summer, and mature into females in July and August.Communicated by M. Kühl, Helsingør     

Energy investment in the annual reproduction cycle of female red porgy, <Emphasis Type="Italic">Pagrus pagrus</Emphasis> (L.)

Seasonal cycle in energy content of gonad, perivisceral fat, liver, and muscle was used to estimate the energy cost of spawning of female red porgy (Pagrus pagrus) from Buenos Aires coasts, Argentina. Spawning was observed primarily between November and January, although a low-intensity spawning was also observed at the beginning of this period. The energy required for gonad development of female red porgy (the difference between the maximum and minimum energy content of ovaries along the year) was 2,652 J g⁻¹ dry weight or 558 kJ. Female red porgy expend 22.8% of their total body energy (3,481 kJ) during the spawning period. Of this energy, relative contributions from different sources were as follows: ovaries 62.5% (496 kJ), perivisceral fat 17.8% (142 kJ), liver 10.3% (82 kJ), and muscles 9.4% (75 kJ). Female spawners lost about 7.2% (119 g) of their total body weight (1,654 g) in the spawning period. From the 7.2% of the total weight lost, female gonad represented a relative reduction of 73.8% (87.6 g), the perivisceral fat declined by 5.7% (6.8 g), the liver declined by 10.6% (12.5 g), and muscle tissue exhibited a 10% loss in total weight (11.9 g). Reproductive effort represented 7.6% of food energy, while resting metabolism accounted for almost 38% of food energy. Despite the fact that red porgy females feed throughout the entire spawning period, it is shown that between pre-spawning (September, water temperature 15°C) and mid-spawning (December, water temperature 19°C) they lost 45 and 38% of their muscle and liver lipids, respectively, and 89% of the perivisceral fat associated with the gut and body cavity. Red porgy used both their energy reserves and food energy during ovarian maturation. This asynchronous species have a strategy of a lower energy allocation and a higher dependence of food during the spawning time (late-spring and summer) for successful reproduction.     

The reproductive cycle of <Emphasis Type="Italic">Scolelepis goodbodyi</Emphasis> (Polychaeta,Spionidae)

The aim of this study was to examine the reproductive and gametogenic cycle of the spionid polychaete Scolelepis goodbodyi (Jones). Every 15 days, in the upper level of the intertidal zone on Barequeçaba Beach in southeastern Brazil, a 100 m² area was delimited and within it three points were selected and sampled using a core sampler 0.01 m² in area × 0.2 m long. Each sample was divided into three sub-samples: surface (2 cm) and middle (8 cm), which were sieved through 0.5, 0.25 and 0.125 mm mesh sieves; and lower (10 cm), sieved through 1.0 and 0.5 mm mesh sieves. Males, females and undetermined individuals were separated, and the width of the third setiger was measured. The gonadal development of each individual was classified based on external features of the gametogenic setigers. Ten to 20 adults from each sampling period were classified according to their gonadal development stage and then analyzed histologically for gametogenic studies, for comparison with the former classification. Some of the ripe females were used for fecundity evaluation. The diameters of the oocytes were measured prior to spawning. Eight hundred and twenty-eight females (29.70%), 848 males (30.42%) and 1,112 undetermined individuals (39.89%) were analyzed. The sex ratio did not differ significantly from unity (χ² = 0.24; df = 1; P < 0.05). Males and females were more abundant in May 2002 (ca. 80%) and between November 2002 and May 2003 (between 77 and 90%); the proportion of undetermined individuals did not represent recruitment alone, but also a high incidence of adults with recovering gonads. Fecundity varied from 134 oocytes in a 0.54 mm W3 individual to 289 oocytes in a 0.4 mm W3 individual, with a mean of 220 (SD = 57) oocytes per female and 19 (SD = 5) oocytes per gametogenic setiger. Oocytes were ellipsoid, and ranged in size from 150 × 80 (to 220 × 120 μm (mean ± SD = 173 × 113 ± 15 × 11 μm). Neither a well-defined gametogenic cycle nor synchrony in the reproductive period was observed, because many gonadal development stages occurred in each month. Nevertheless, peaks of maturity were observed between October–December 2002 and April–May 2003.     

Histology of the gonads and observations on the social behavior of the Caribbean angelfish Holacanthus tricolor

Male and female specimens of Holacanthus tricolor were collected in May 1981 and September 1982 off the Island of St. Croix. U.S. Virgin Islands, and their gonads were examined histologically. All testes examined showed vasa deferentia which were characteristic of secondary males, suggesting protogynous sex change. A transitional individual supported this interpretation. Ovarian histology and size-specific egg counts revealed seasonal differences in spawning frequency and clutch size. Females appeared to spawn every day in May. The timing of final maturation and hydration of the oocytes indicated that spawning occurred in the late afternoon or early evening. Not all females spawned every day in September, and clutch sizes were smaller than those of May. Behavioral observations of H. tricolor in the field revealed that males defended harems of two to four smaller females. Within each harem, females of different sizes had overlapping home ranges, while the home ranges of females of similar size did not overlap. Besides size dimorphism between the sexes, H. tricolor exhibited a previously unreported sexual dichromatism.     

Histological investigation of the reproductive cycles of the limpets <Emphasis Type="Italic">Patella </Emphasis><Emphasis Type="Italic">vulgata</Emphasis> and <Emphasis Type="Italic">Patella ulyssiponensis</Emphasis>

This study devised a staging system for, and monitored, the gonad development of the limpet species Patella vulgata and Patella ulyssiponensis on the South West coast of Ireland using histological techniques. Maturation began in the males of both species in January and in the females it began in March. There was no statistical difference in gonad development between sexes and between species. Spawning in the male P. vulgata occurred from September to December 2003 and in September and October 2004. In female P. vulgata spawning occurred from October to December 2003, no spawning of females was observed in 2004. In male P. ulyssiponensis spawning occurred in November and December 2003 and from September 2004 to December 2004. Spawning was observed from November 2003 to January 2004 and in September 2004 in female P. ulyssiponensis. Sex ratios also varied between the species and between months sampled. Nevertheless more males were observed in both species.     

Gametogenesis and spawning periodicity in the fan worm <Emphasis Type="Italic">Sabellastarte spectabilis</Emphasis> (Polychaeta: Sabellidae)

The sabellid polychaete Sabellastarte spectabilis (Grube 1878) was collected at approximately monthly intervals from January 2002 to December 2003 from intertidal and subtidal reefs near the Hawaii Institute of Marine Biology in Kane’ohe Bay, Hawaii, USA (21°N, 157°W). Gametogenesis and spawning periodicity were investigated using histological techniques and induction of spawning trials. Worms were characterized into four discrete reproductive stages based on histological evidence: (1) No evidence of reproductive activity in the coelom (sex cannot be determined), (2) Only coelomocytes present in the coelom (sex cannot be determined), (3) Some gametes present in the coelom (sex can be determined) and (4) Coelom densely packed with gametes (sex can be determined). The small hermaphroditic portion of the population was not used in this study. Stage 4 worms were present over an extended period of time (females, March–December and males, March–November) indicating a potentially broad reproductive season. No correlation between day length and maturation stages in S. spectabilis was detected. However, the statistical model Y = ([394.26 × X] − [7.793 × X ²]) − 4960.781 where Y the % frequency of Stage 4 worms and X the mean monthly water temperature explained 44% of the variation between water temperature and % frequency of Stage 4 worms. Maturation appeared to coincide with water temperatures of 24–25°C (March–September) after which there is a reduction in the % frequency of stage 4 individuals. Induction of spawning trials conducted between May and January showed the month of October with a significantly higher percent success than any other month investigated. According to all available information (e.g., natural spawning in water tables, histological data, induction of spawning trials, correlation of maturation stages with observed changes in average monthly water temperature.), there is an apparent peak in reproductive activity (spawning) within a broad maturational season, which may be influenced by water temperature.     

Offshore spawning by the portunid crabScylla serrata (Crustacea: Decapoda)

The portunid crabScylla serrata (Forskål) is shown to migrate offshore to spawn. Records of 447S. serrata caught as bycatch by trawlers in the tropical waters of northern Australia were analysed with respect to area, depth, distance offshore and month of capture as well as the sex and size of the crabs and whether the females were ovigerous. The crabs were caught mainly in three areas that correspond to the tiger prawn trawl fishery, at between 10 and 60 m depth (mean 28.5 m), 3 to 95 km offshore (mean 17.9 km). Most (87%) of the crabs were captured in October and November, which suggests they move offshore in September and October. No crabs were reported from offshore by February. Over 97% of the crabs caught offshore were female, of these 61.5% were ovigerous. The size range of females (100–109 to 200–209 mm carapace-width size classes) and males (120–129 to 200–209 mm carapace-width size classes) caught was similar. The frequent occurrence in coastal waters of females that are larger than the modal size at spawning, as well as mature females with spent ovaries, suggests that many females return to the coast after spawning. Although some species of portunid crab are euryhaline, mature females of estuarine species migrate to the sea to spawn. The migration byS. serrata described here is far more extensive than would be required to reach sea water salinities; it probably provides a dispersal mechanism for larvae to enable the megalopa stage to recruit to habitats distant from those of the parents.