Taxonomy of the deep-sea eel genus, Histiobranchus (Synaphobranchidae, Anguilliformes), with notes on the ecology of H. bathybius in the eastern North Atlantic

The eel genus Histiobranchus Gill occurs benthopelagically over the continental rise and abyss of the World Ocean, primarily beneath temperate and subpolar surface waters. Its generic status within the subfamily Synaphobranchinae is confirmed by comparison of the structure and topography of its cephalic sensory system and skeletal features with Synaphobranchus. At least three species of Histiobranchus are recognized: H. bathybius (panoceanic), H. bruuni (Tasman Sea and waters south-east of New Zealand) and H. australis (two geographical forms; South Atlantic and south-western Indian Ocean, and South Indo-West Pacific Oceans). Collections totalling 319 specimens of H. bathybius from the eastern North Atlantic (1790–5440 m depth) yielded a size range of 99–1370 mm total length ( L _T), with no apparent sexual dimorphism. Length–frequency distributions indicate a mode of juvenile fish at around 100–200 mm L _T and a further two around 600–700 and 1300–1400 mm L _T among adults. Generally smaller fish occur in shallower regions, although the size range is broad over the whole depth range. No apparent trend occurs in the size distribution with latitude over the range 17–54) N. Females outnumber males (1 male : 1·7 females) and both sexes are largely distinguishable from 300 mm L _T. Ripening eggs occur in females from both adult length modes, with running ripe and spent females of very different size indicating iteroparity.     

Spawning characteristics of the anadromous brown trout in a small Swedish stream

The spawning pattern of the anadromous brown trout Salmo trutta was studied in Själsöån, a small stream in Gotland, Sweden, during eight winters between 1992–1993 and 1999–2000. The total length ( L _T) at spawning was normally distributed (185–890 mm) for females and multimodal for males (300, 400 and 550 mm most frequent length classes). Spawning males were significantly younger (2+ to 4+ years) than females (3+ to 5+ years). The sex‐ratio at the beginning and at the end of the spawning season favoured males. The mean ±  s . d . number of spawners was 70 ± 16 individuals per year. Migration into and out of the stream occurred between November and June. The highest number of spawning fish was found in the stream at the end of November or at the beginning of December. Migration mainly occurred during high water flow and at night. The majority of the females entered the stream and spawned the same (29·3% of all the females) or the next night (32·8% of all the females) while males may have stayed for 2 to 3 weeks (21·3% of all the males) in the stream before spawning. Males usually remained much longer in the stream (mean ±  s . d . 45 ± 56 days) than females (16 ± 30 days). Females lost more mass in the stream (mean ±  s . d . 17·3 ± 8·6%) than males (7·7 ± 9·6%). For both sexes, mass loss was positively correlated with the time spent in the stream. Only 7·3% of the males and 5·7% of the females occurred in the stream for >1 year. Spawning took place only during the night.     

Maturation, fecundity, and intertidal spawning of Pacific sand lance in the northern Gulf of Alaska

Pacific sand lance Ammodytes hexapterus in Kachemak Bay, Alaska, showed no sexual dimorphism in length-to-weight (gonad-free) ratio or length-at-age relationship. Most matured in their second year, males earlier in the season than females, but females (31%) attained a higher gonadosomatic index than males (21%). Sand lance spawned intertidally once each year in late September and October on fine gravel or sandy beaches soon after the seasonal peak in water temperatures. Sand lance in Cook Inlet and Prince William Sound displayed similar maturation schedules. Schools were dominated 2: 1 by males as they approached the intertidal zone at a site where spawning has taken place for decades. Sand lance spawned vigorously in dense formations, leaving scoured pits in beach sediments. Fecundity of females (93–199 mm) was proportional to length, ranging from 1468 to 16 081 ova per female. About half of the overall spawning school fecundity was derived from age group 1 females (55% of the school by number). Spawned eggs were 1·02 mm in diameter, demersal, slightly adhesive, and deposited in the intertidal just below the waterline. Sand lance embryos developed over 67 days through periods of intertidal exposure and sub-freezing air temperatures.     

Reproductive biology of the endangered Oxleyan pygmy perch Nannoperca oxleyana Whitley

The reproductive biology of the Oxleyan pygmy perch Nannoperca oxleyana is described from simultaneous studies of wild populations in north-eastern New South Wales and mature fish held in aquaria. In the wild, 50% of males and females matured at total lengths of 24·0–25·9 and 28·0–29·9 mm, respectively. The species displays sexual dichromatism during the spawning season, with males developing more intense red and brown fin and body colouration, and black pelvic fins. Captive male broodfish displayed territoriality during the breeding season, closely guarding sites within artificial, plant-like substrata in which pairs of fish spawned adhesive eggs. Protracted serial spawning of wild and captive fish occurred from September to April and May at mean water temperatures ≥16·6° C and day length ≥10·7 h. Captive broodfish spawned on an average of 57% of days during the 256 day spawning period. Gonado-somatic indices averaged 0·7% for all ripe males and 4·1–4·2% for all ripe females collected. Mean total and batch fecundities of captive females were 1323 eggs per fish and 7·8 eggs per fish per day, respectively, and relative fecundity was 587 eggs g⁻¹ of body mass. Batch fecundity of wild females was estimated at 7·8 eggs per fish. The adaptive significance of this reproductive strategy in a harsh, variable environment is discussed.     

The relation between feeding and reproduction in Anasterias minuta (Asteroidea: Forcipulata)

Anasterias minuta is an oral-brooding sea star and one of the main predators of intertidal benthos in Patagonia, Argentina. The aims of this study were to: (1) assess the temporal pattern of feeding and brooding, (2) evaluate the effect of body size, tidal height and temperature on feeding and brooding, (3) evaluate temporary changes in digestive and sexual organs and (4) investigate the relationships between the predatory and brooding activities. Females do not feed during the brooding period. Spawning proceeded during March. The brooding period was from March to November, with a maximum in May. The population feeding rate varied seasonally, with a maximum in December and a minimum in May. The feeding rate was positively related to water temperature and sea star size; but not with tidal height. An annual cycle exists for pyloric caeca weight in both sexes; lowest values were found during winter, due to brooding female starvation, and a possible decrease in feeding rate of non-brooding females and males. No inverse relationship was found between the pyloric caeca and gonad weights in females, but a lag of 1 month was observed in males, being the maximal pyloric caeca development before the maximum gonad weight, suggesting nutrient translocation.     

The reproductive ecology and abundance of Symptevygia bonapavtii endemic to the south-west Atlantic

Logistical ogives gave an estimated L _T50 value (i.e. the total length at which 50% individuals are sexually mature) of 635 mm for female and 650 mm for male Sympterygia bonapartii . Mature individuals of both sexes had significantly larger livers than immature ones and females had a significantly heavier liver than males. Clasper elongation was the first step in male maturation, followed by clasper calcification and the development of alar thorns. In mature females, the right ovary was larger than the left, which was apparently due to differences in stroma tissue. Gonadosomatic index and diameter of ovarian follicles of mature females peaked in late spring and was at a minimum from late summer and through the winter. Juvenile S. bonapartii were more abundant near estuarine areas during winter, and adults appeared in estuaries by late spring and summer. Females carrying egg-cases were found near the shore in late spring and egg-cases were found in benthic samples only in shallow waters suggesting that S. bonapartii deposits egg-cases in shallow waters during late spring-summer and that nursery areas are in outer estuarine zones. In the southern part (38°–42° S) of the study area S. bonapartii showed a strong movement to shallow waters in late spring and summer, spreading over the entire coastal area in winter. These movements are discussed in relation to water temperature and trophic interactions.     

The movements of pikeperch in a shallow reservoir

The movements of 12 female (62–74 cm) and eight male pikeperch (55–64 cm) radiotagged in early March 1997 in the shallow and turbid Bygholm Reservoir, peaked during the summer, but all fish were also active during the winter. Females moved more than males and their activity was correlated with water temperature. Rate of movement was correlated positively with body size for both male and female pikeperch. During the breeding season (April–May) males became stationary for 14–47 days. Spawning sites, inferred from movements of males, were at depths of 2·0–2·5 m on hard substrata, mainly gravel in areas with many submerged trees and shrubs. Males tended to use the same spawning site the next year. Diel activity pattern varied seasonally but activity was highest from 1800 to 2400 hours.     

Phenotypic sex differentiation of blue tilapia under constant and fluctuating thermal regimes and its adaptive and evolutionary implications

Oreochromis aureus exposed during the first 28 days of exogenous feeding to constant 35° C, or fluctuating temperatures (day at 35° C, night at 27° C, and vice versa) showed significantly ( P <0·05) faster growth, least size heterogeneity and better survival rates than siblings under constant 27° C. Constant high temperatures had a strong masculinizing effect (M: F sex ratios of 7·33–19·00: 1·00 v . 0·75–0·82: 1·00 in controls reared at 27° C). Fluctuating temperatures had less masculinizing potential but still produced sex ratios significantly skewed to the detriment of females (M: F sex ratios of 2·33–11·50: 1·00). This suggests that ambient temperature may have represented a sufficient environmental pressure for the selection of thermolabile sex-determinism in this species, and presumably in other Oreochromis spp. The evolutionary advantage of thermosensitivity in Oreochromis spp. is discussed, considering a framework where individual advantages oppose, to some degree, to the population or species interest.     

Distribution and reproduction of the southern lantern shark from New Zealand

Distribution, population structure and reproduction are described for the southern lantern shark Etmopterus granulosus at the Chatham Rise, New Zealand. Depth of capture for E. granulosus ranged from 744 to 1420 m, with highest catch rates between 800–1200 m. More than twice as many females as males were captured, and the majority of sharks caught were mature, indicating that there may be segregation according to sex and size class. Only 10 of 492 female sharks captured contained ova in uteri, and none contained embryos. The absence of pregnant females suggests that they move to another area or depth prior to pupping. Size of sharks captured ranged from 20·0 to 78·8 cm total length. Females began to mature at 62 cm total length, and males at 52 cm. There was no evidence of a seasonal reproductive cycle. Ovulation appeared to occur when ova reached a diameter of 40–45 mm. The average number of ova in mature females was 12·7. This information is crucial for assessing the impact of fisheries on E. granulosus populations.     

Reproductive biology of the threatened golden galaxias Galaxias auratus Johnston and the influence of lake hydrology

Golden galaxias Galaxias auratus (31–235 mm fork length, L _F) were collected monthly from littoral habitats in Lakes Crescent and Sorell, Tasmania, Australia, between July 2000 and December 2002. Spawning habitats were identified and monitored in both lakes, and surveyed in Lake Crescent. Trends in gonado-somatic indices and reproductive stages of development indicated that gonad development in both sexes begins in midsummer and peaks in late autumn to early winter. Males mature at smaller sizes (50% at 52 mm L _F) than females (50% at 76 mm L _F), larger individuals are predominately females (95% of fish ≥138 mm L _F), and overall male to female ratios are female biased ( c . 1:2). Spawning occurs late autumn to early spring (water temperatures = 1·4–9·7° C) with peaks in spawning activity in winter (mean water temperatures <5° C). Demersal adhesive eggs ( c. 1·5 mm diameter) were found on cobble substrata ( c. 20–250 mm diameter) in littoral areas ( c. 0·2–0·6 m deep) and fecundity of fish 71–181 mm L _F ranged from 619 to 14 478 eggs. The rate of change in water level over the 20 days prior to monthly sampling was important in explaining the occurrence of spent fish and this accounted for temporal differences in spawning between the populations. Lake hydrology influences the reproductive cycle of G. auratus by possibly providing a stimulus for spawning and it controls the availability of spawning habitat in Lake Crescent. Seasonal hydrological cycles ( i.e. rises during late autumn to winter) and a minimum water level of 802·20 m Australian Height Datum in Lake Crescent during autumn (above which littoral areas of cobble substratum are inundated) are critical to G. auratus populations.     

Reproduction in the dusky grouper from the southern Mediterranean

Demographic data and gonad histology confirmed that the dusky grouper Epinephelus marginatus is a protogynous hermaphrodite that follows a monandric pathway to sexual development. Females reached first sexual maturity at 36·7 cm L_s and estimated mean length at first maturity (L₅₀) was 43·8 cm L_s for females and 81·3 cm L_s for males. Adult sex ratios during the reproductive period were c. 3·5: 1 females to males. Females exhibited group-synchronous ovarian development and multiple ovulation occurred over the spawning period. Gonads were ripe from early May and spawning occurred from June until early September. The size of ripe testes (0·6% W )indicated strong oligospermy and suggested a mating system with no sperm competition. Sexual transition was protogynous involving regression of ovarian tissue and proliferation of testicular tissue in the gonads. Transitional individuals occurred from May through November and accounted for 9% of sampled adult population. Sex change occurred in fish 69–93 cm (L_s) long and the size distributions of males and females overlapped over 27% of the L_s range. Special zones were recognized as gathering areas for sexually mature dusky groupers during the reproductive period.     

Reproductive biology of Vinciguerria nimbaria in the equatorial waters of the eastern Atlantic Ocean

Adult Vinciguerria nimbaria in an area of the Atlantic Ocean (0–5°N; 10–20°W), collected from November 1994 to February 1998, exhibited two different patterns in diel behaviour: 'typical' behaviour which consisted of large diel vertical migration and 'atypical', characterized by concentrations of schools that remained in the surface layers during the daytime. The total life span of V. nimbaria was estimated at 6–7 months. Females were mature when they reached 30·6 mm standard length ( L _S), which corresponded to an age of 85 days. Once the females were mature, spawning was continuous in the population as a whole, and V. nimbaria spawned continuously throughout the year. Spawning took place during two restricted times of the day: typical females spawned at dusk and atypical females spawned at dawn. Using the post-ovulatory follicles method, spawning frequency was estimated at 2 days. Batch fecundity was estimated at 1236 oocytes or 1230 oocytes g⁻¹ of total body mass, and egg size was 650 µm whatever the period of the year. The lifetime fecundity of V. nimbaria was estimated at 9000 eggs (109 000 eggs if mortality rate was not taken into account), and the maximum stock egg production of a theoretical cohort occurred at 37 mm L _S. Young adults thus contributed the most to the reproductive output for the survival of the population.     

Seasonal changes in the habitat use and movements of adult European grayling in a large subarctic river

In late summer (13 August–13 September 1998), at water temperatures of 12·0–15·7° C, grayling ( n =14) stayed mainly in the riffle-section where they were captured in a large regulated river in northern Finland, moving little between consecutive days. In autumn (2–30 October 1998), at 1·7–6·7° C, the fish ( n =16) migrated to potential overwintering sites 0–14 km up- or downstream by mid October, moving mainly short distances thereafter. The daily movement rates, and the total ranges covered by the fish in late summer and autumn were 54±32 m (mean± s.d ) and 1053±1636 m, and 190±168 m and 3135±1850 m, respectively. In autumn the fish used deeper habitats (most suitable range 150–400 cm) with lower current velocities (20–80 cm s⁻¹) and finer bottom substrata (mainly sand) than in late summer (depth 100–325 cm, velocity 30–110 cm s⁻¹, and cobble-boulder substrata).     

Reproduction of the blue-spotted maskray Neotrygon kuhlii (Myliobatoidei: Dasyatidae) in south-east Queensland, Australia

This study examined the reproduction and population structure of the blue-spotted maskray Neotrygon kuhlii within Moreton Bay, a subtropical embayment in south-east Queensland, Australia. Mean sizes at maturity were 314 mm disc width ( W _D) in females ( n = 140, 115–465 mm W _D) and 294 mm W _D in males ( n = 123, 129–381 mm W _D). Female N. kuhlii had a synchronous annual reproductive cycle, with one litter of one to three pups (mean ± s.d . 1·67 ± 0·71) produced per year. Mating behaviours were observed in October and November, and ovulation occurred early in the Austral summer, overlapping with the start of embryonic development. Gestation took c. 4 months with parturition occurring in late February and March. Size at birth was 115–170 mm W _D. The population showed a significant female bias, particularly in larger size classes. Tagging studies produced a total recapture rate of 16·1% and indicated that N. kuhlii were site resident for up to 1081 days.     

Feeding behaviour of yearling and older hybrid grass carp

Hybrid grass carp resulting from the cross of a female grass carp, Ctenopharyngodon idella (Val.), and a male bighead carp, Hypophthalmichthys ( Aristichthys ) nobilis Rich., 12–18 months old ( c . 300 mm T.L.) were studied in a two-part experiment to determine feeding preference and total daily consumption fish^-1 on selected species of aquatic plants. Fish were maintained in circular pools with 6840·8 1 of water inside a temperature-controlled greenhouse. Preference tests were conducted at three temperature ranges; 25–28° C, 17–20° C and 12–15° C. Based on the time to complete consumption or the relative quantity consumed, the most preferred plant was Lemna gibba when in combination with six other species. Chara sp., Najas guadalupensis and Potamogeton peciinatus were readily consumed and considered to be of about equal preference. Ceratophyllum demersum and Myriophyllum brasiliense were least preferred. Hybrid grass carp generally consumed as much plant material species^-1 and in the same order of preference at the 12–15°C range as they did at 25–28° C. In the second part, mean daily consumption (g) fish^-1 at 25·7–31·0° C for five plant species tested separately was as follows: Chara sp. 369·8; Lemna gibba 178·2; Najas guadalupensis 172·6; Hydrilla verticillata 106·4 and Ceratophyllum demersum 8·8.     

Age, growth and reproduction of the barrelfish Hyperoglyphe perciformis (Mitchill) in the western North Atlantic

Otoliths ( n = 847) and gonads ( n = 817) were collected from barrelfish Hyperoglyphe perciformis that were captured by commercial fishermen in the waters off South Carolina and Georgia in 1995, 1997 and 2001–2006. Of the otoliths collected, 97% were aged successfully, and specimens sampled ranged from 5 to 85 years, with a median age of 12 years. The von Bertalanffy growth parameters yielded the equation: L_t = 857·8{1 − e^{−0·0985[ t −(−8·95)]}}, where L_t is fork length ( L _F) at time t . Through histological examination, 94% of the gonads assessed were assigned to a sex and reproductive class. Females spawned from September to May with a peak from November to January. Males spawned year round, but had a peak from September to April. The sex ratio (M:F) for this population was 1:1·34. The smallest mature female was 605 mm L _F and the youngest immature female was 697 mm L _F. Estimates of L _F and age at 50% maturity ( L ₅₀ and A ₅₀) for females were 660 mm L _F (95% CI = 633–667 mm L _F) and 6·08 years (95% CI = 3·50–7·27 years), respectively. The youngest mature male was 575 mm L _F and the oldest immature male was 762 mm L _F, and no estimates of L ₅₀ or A ₅₀ were made for males. It was determined that barrelfish exhibit the typical characteristics of long life span, slow growth and high age at maturity seen in other deepwater fishes, and that care should be taken to manage this species accordingly.     

The length weight relationship, age, growth and reproduction of the roach Rutilus rutilus (L.) in Lake Volvi

The length-weight relationship of a sample of 233 roach ( Rutilus rutilus ) can be described by the following equations: y =0·0356 x ^3·405 and y =0·0215 ×^3·606 for males and females respectively. In both equations y equals the body weight in grams and × is the standard length in centimetres. The average condition factor K was 2·01 with a range of 1·71 to 2·26. The roach's span of life was 13 years for both sexes. The growth increment is greater during the first year of life (about 56 mm), decreasing to approximately 17 mm at the end of the sixth year of life and then becoming constant at about 12 mm per year. Roach become sexually mature at age 1 + for males and one year later for females. The mean absolute fecundity was 9294 eggs; with a range from 920 to 32 810. The growth of the gonads is related to the age of the fish. Spawning occurs during the first half of April, at a mean water temperature of 10° C.     

Reproductive biology of the smooth-hound shark Mustelus mustelus (L.) in the Gulf of Gabès (south-central Mediterranean Sea)

The reproductive biology of the smooth-hound shark Mustelus mustelus was studied in the Gulf of Gabès (southern Tunisia). Females were found to mature between 1075 and 1230 mm total length ( L _T) whereas males matured between 880 and 1120 mm L _T. The L _T at which 50% of the population reached maturity was 971 and 1172 mm for males and females, respectively. Male gonads were symmetrical in terms of mass and both functional, whereas in females only the right ovary was functional. The seasonal changes in the oocytes and testes development, embryo length and the occurrence of near-term and post-partum females showed that this species displayed a clearly defined annual reproductive cycle with parturition occurring during late April and early May, after a gestation period of 10–11 months. Mating took place during May and early June and fertilization occurred from early June to early July. The embryo sex ratio was not significantly different from unity. Litter size varied from four to 18 embryos and was positively correlated with maternal L _T. The young were born with a L _T of 340–420 mm.     

Reproductive biology of Psammobatis extenta

Psammobatis extenta collected from the commercial bottom trawl fishery operating in Puerto Quequén, Argentina, between 2000 and 2001, had a sex ratio of 1:1 (535 specimens). Both the largest male and female measured 313 mm total length ( L _T). The relationship between total body mass and L _T was significantly different between sexes; mature females weighed more than mature males for a given L _T. The size at which 50% of males were sexually mature was 262 mm L _T (83·6% of the maximum size), whereas 50% of females were mature at 249 mm L _T (80·0% of the maximum size). The gonadosomatic index in mature males and females was slightly higher during summer, but did not show significant variation over the sampling period. The hepatosomatic index of males and females was higher during the autumn and winter and followed a distinct seasonal pattern. Evidence suggested a continuous reproductive cycle during the year, with a maximum number of females carrying egg-cases in summer.