Age, growth, reproduction and mortality of the striped seabream, Lithognathus mormyrus (Pisces, Sparidae), off the Canary Islands (Central-east Atlantic)

Striped seabream, Lithognathus mormyrus L. (n=731) caught off the Canary Islands from January 1999 to June 2000 were studied. Fish ranged in size from 113 to 372 mm total length, weighing from 21.1 to 748.2 g total weight. Weight increased allometrically with size (b=2.9071). Fish age was 0–10-years-old. Growth was relatively slow (k=0.88 years⁻¹), with females growing at a slightly faster rate than males. The species displayed protandric hermaphroditism. Male : female ratio was unbalanced in favour of males (1 : 0.85). Males predominated in smaller sizes, females in larger sizes, and intersexual individuals were in intermediate sizes. The reproductive season extended from June to December, with a peak in spawning activity in August–September. Males reached maturity at 207 mm (2 years) and females at 246 mm (3 years). The real value of instantaneous rate of natural mortality was between 0.30 and 0.45 years⁻¹.     

The growth of charr, Salvelinus willughbii Günther, in Windermere

The growth of charr ( Salvelinus willughbii Günther ) caught in Windermere from 1941–1952 has been studied. Scales were used for determination of age and back-calculation of length for age. Autumn and spring spawners, males and females, and charr of normal and dwarf growth were treated separately. In fish of normal growth, the spring spawners were significantly smaller than the autumn spawners at ages 1 and 2 years, and significantly larger from age 4 years onwards. There was little difference in growth between males and females within the two spawning populations. Charr of lengths of less than 200 mm at age 4 years were considered to be dwarfs. Mean lengths at capture of male charr were: autumn spawners normal growth 272 mm, dwarf 218 mm; spring spawners normal growth 327 mm, dwarf 194 mm. The oldest recorded age was 8 years.     

Fluctuating recruitment and variable life history of migratory brown trout, Salmo trutta L., in a small, unstable stream

The recruitment dynamics and life history of migratory brown trout, Sulmo trutta L., were investigated in a small Baltic coast stream subject to recurring drought. Spawning males consisted of both mature male parr (101–206 mm t.l. ) and migrant males (205–780 mm t.l. ). Spawning females were all migrants which delayed maturity until reaching a significantly greater size on average (424–805 mm t.l. ) than migrant males. Male: female ratios were very high in spawning aggregations (9–12 males: 1 female) with males representing up to five year-classes or more. Gametes from several generations of males per spawning event may be important for maintaining the genetic viability of this population with few female spawners per year. The amount of spawning was dependent on precipitation just prior to and during the spawning period since migrants could not enter the stream under drought conditions. Migrants did not overwinter in the stream.
Drought also caused variable fry mortality following emergence in early summer. Recruitment of 0+ parr in autumn varied from c . 175 to 3000 during 3 years. Smolts were relatively young (ages 1–2) and small (≥8 cm), and were significantly longer on average than sibling parr. Yet emigration of 1-year-olds was not related to 0+ parr size the previous autumn because of overlapping growth rates.
Persistence of the migratory brown trout in this unstable environment may be the consequence of (i) life history adaptation (e.g. short freshwater residence of both juveniles and spawners), and (ii) a complementary set of individual life histories where variation in age of migrant spawners and the occurrence of mature male parr result in a stable spawner population despite inconsistent recruitment of migrants to the sea.     

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.     

Otolith description and age‐and‐growth of Kurtus gulliveri from northern Australia

The sagitta of Kurtus gulliveri was ovate, moderately thick with the following attributes: lateral surface convex, mesial surface flat; dorsal margin sinuate, posterior margin rounded ventrally, ventral margin rounded and irregular; sulcus divided into ostium and cauda by constriction of dorsal and ventral margins, heterosulcoid, colliculum heteromorph; dorsal depression large and distinct, ventral groove close to margin in larger otoliths; rostrum broad and antirostrum small, separated by wide, shallow excisural notch. Otolith size was moderate, average 4·6% standard length ( L _S), typical for a perciform. Annuli on 78 whole sagittae were read, and 15% of these were transversely sectioned for verification of the annuli. Males ranged from 94 to 235 mm L _S and females from 95 to 284 mm L _S. There was little difference in size distribution of the sample between the sexes, perhaps due to a 6 month spawning season over which young were continually added to the population. Some sexual dimorphism was noted, however, as age 2 year females were significantly larger than males of the same age. The largest fish aged was a 284 mm L _S, 3 year‐old female, and the oldest age reached was 4 years by two males. It appears likely that most spawning females are ≥2 years old, but some larger 1 year old fish may attain sexual maturity.     

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.     

Biology of the annular seabream, Diplodus annularis (Sparidae), in coastal waters of the Canary Islands

The biology of the Canary Islands annular seabream Diplodus annularis (Linnaeus 1758) was studied from samples collected between January and December 1998. Fish ranged from 82 to 209 mm total length in size and from 8.7 to 137.1 g in weight. The mean length showed an increase with increasing water depth. Males showed a negative allometric growth and females isometric growth. The species was characterized by protandric hermaphroditism. The overall sex ratio was unbalanced in favour of males (1 : 0.79). The reproductive season extended from January to May, with a peak in spawning activity in March–April. Males reached maturity at a smaller length (103 mm, 1-year-old) than females (128 mm, 2-year-old). Fish aged 0–6 years were found. The von Bertalanffy growth parameters for all individuals were: L_∞=247.9 mm, k=0.268 years^–1, and t₀=–0.879 years.     

Growth of dark chub, Zacco temmincki (Cyprinidae), with a discussion of sexual size differences

I examined the annual and seasonal growth of dark chub, Zacco temmincki, in a Japanese river. Investigation of opercular rings showed that the fish reached a maximum age of 8 years. There was no significant sexual size difference at younger ages (3–5 years), but males were larger than females at older ages (6–7 years). Annual increments of length and weight for males that were recaptured were also larger than those for females. The fish spawn from June to August. Females grew for a short period from April to May, but males on average grew for a longer period from April to August. There was no sexual difference in growth rate except during the spawning period. Annual growth rate was negatively correlated with fish length in each sex. The sexual size differences at older ages of the fish might be due to the polygynous mating system in which most mature males could not obtain females and invested for somatic growth in the spawning period, and a short growing season that was overlapped considerably with the spawning period.     

Growth and life history traits of Aegean chub,Squalius fellowesii (Günther, 1868) in streams in Muğla Province,Aegean coast,Turkey

To aid in species' conservation, the aim of this study was to provide initial findings on age, growth and reproduction of an endemic species, Aegean chub Squalius fellowesii (Günther, 1868) populations from streams in the Aegean region of Mu?la Province, Turkey. The species is relatively short‐lived (maximum 6 years), attaining a size of about 200 mm total length with a rapid growth to first maturity (≈60 mm TL), and relatively little growth thereafter. The male:female ratio was 1.0 : 0.6, males significantly outnumbering females in the majority of the streams. General condition values of individual fish varied between 2.9 and 3.4. Sexual maturity was usually achieved later and at larger sizes in females than in males. Sexual maturation in most populations was at the age of 2 years in females and 1 year in males. The species spawns between early April and late May. Mean absolute and relative fecundity were about 4440 eggs and 57 eggs·g^?1, respectively. Mean egg diameter was 1.00 ± 0.03 mm, ranging from 0.70 to 1.20 mm. Suggestions for the conservation of Aegean chub are discussed.     

Reproductive biology of racer goby Neogobius gymnotrachelus in the Włocławski Reservoir (Vistula River, Poland)

Initial studies on the reproductive parameters and spawning behaviour of racer goby Neogobius gymnotrachelus, one of three Ponto‐Caspian gobiid species recently invading Polish waters, were carried out in W?oc?awski Reservoir (lower River Vistula, Poland), where spawning lasted from April to August. Males were on average about 23.3% longer and 53.8% heavier than females. The smallest female with mature gonads was 58 mm TL (estimated age 2+ years), and males were sexually mature at 59 mm TL (age of 1+ years). Gonado‐somatic index at the beginning of spawning was seven times larger in females (mean = 8.4) than that in males (mean = 1.2). Mean absolute fecundity was 952 eggs per female (361–2236). Egg diameter ranged from 0.140 to 1.558 mm, being of bi‐modal distribution, which suggests two or three spawning bouts. Length–frequency analysis of juveniles revealed a multimodal distribution. Specialized reproductive behaviour (nest construction and parental care of eggs) and an extended spawning period increase the probability that racer goby can successfully establish self‐sustaining populations in novel environments.     

The reproductive biology of blackspot sea bream Pagellus bogaraveo in captivity. I. gonadal development, maturation and hermaphroditism

Gonadal development, maturation, spawning and hermaphroditism were investigated in captive blackspot sea bream, Pagellus bogaraveo Brünnich, 1768, during the second, third and fourth years of life. The gonads of 224 fish were examined macroscopically and histologically. Undifferentiated gonads were found in fish smaller than 22.0 cm. Adult fish showed four gonadal differentiations: ovotestes with functional testis and quiescent ovary (Mf), ovotestes with functional ovary and regressed testis (mF), ovotestes with both ovary and testis at a resting stage (mf), and ovaries with no male tissue (F). The overall incidence of gonochoric females F was 41%. Functional males Mf were more frequent in age classes 1+ and 2+, whereas functional females mF predominated in the 3+ age class, above 25.0 cm TL. Histological examination revealed testicular degeneration and atrophy in functional females mF. On the basis of both histological data as well as size and age frequency distribution, it is suggested that the reproductive strategy of P. bogaraveo in captivity is characterized by protandrous hermaphroditism, with a high incidence of female gonochorism. Spawning occurred in March–April, at a size of 28.0 cm and age 3 in males and at 29.5 cm and age 4 in females. The gonosomatic index (GSI) remained constantly low (≤ 0.05) throughout the second and third years of life. A significant increase in GSI was noted in both males and females at the accomplishment of the fourth year of life, coinciding with the spawning season. The results are compared with information available on wild P. bogaraveo and discussed with a view to a possible exploitation of this species in aquaculture, through a reliable control of reproduction.     

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).     

Age estimation,growth and maturity of the Argentine hake (Merluccius hubbsi Marini, 1933) along the northernmost limit of its distribution in the south-western Atlantic

Age, growth and length-at-maturity of the Argentine hake (Merluccius hubbsi) were studied in the northernmost limit of the species distribution in the south-western Atlantic. A total of 351 otoliths and information from 1610 specimens sampled from the industrial double-rig trawl landings between May 2013 and April 2014 were used. Age and growth were estimated by counting and measuring increments in sectioned sagittae otoliths, and length at maturity was estimated based on macroscopic gonadal analysis. For both sexes, hepatosomatic index and condition index increased mainly during spring, reaching a maximum at the end of summer before the subsequent spawning season began. Gonadosomatic index was highest in April, believed to correspond with peak spawning. The annual periodicity of alternate opaque and translucent zones was validated by marginal increment analysis. Growth curves were fitted to back-calculated size at age by fitting the three-parameters von Bertalanffy growth function. The maximum age was 5 years in fish of either sex. Females attained larger sizes than males. The parameters of the von Bertalanffy growth equations were: L∞?=?533?mm, k?=?0.231 year^?1 and t₀?=??0.935 year for females; L∞?=?394?mm, k?=?0.405 year^?1 and t₀?=??0.463 year for males. The mean length and age at first maturity was 273?mm at 1.9 years for males and 274?mm at 2.0 years for females.     

Regional and interannual variations in spawning activity of Pacific saury Cololabis saira during northward migration in spring in the north-western Pacific

Regional and interannual variations in spawning activity of Pacific saury Cololabis saira during the northward migration in spring were investigated for 1995–1997 in the north-western Pacific. Only females with a large body size (≥270–290 mm knob length) appeared to spawn. Almost all females in this cohort were actively spawning in a region of sea surface temperature ( T _SS) >18° C, the proportion of active spawners appeared positively related to T _SS in a region of 13° C < T _SS≤ 18° C, and no females were spawning in the region of T _SS≤13° C. Although this relationship between spawning activity and T _SS was common in all years, the distribution of females in the large-size cohort among the regions varied interannually. Consequently, the proportion of active spawners among adult females showed considerable interannual variations.     

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.     

Monitoring population productivity in the saiga antelope

Effective conservation requires a good understanding of factors causing variation in population growth rate. We here analyse the relationship between female age and fecundity in the saiga antelope Saiga tatarica tatarica , a critically endangered ungulate of the Eurasian steppes and semideserts, at both individual and population levels. Annual variation in age structure and twinning rates was investigated using long-term datasets, sampling a total of 3308 females in four populations over more than 40 years. Further, a new non-invasive method is presented, estimating twinning rates from both calves and placentas encountered during calving aggregation transects. At an individual level, the most parsimonious model for twinning rates included three age classes (1, 2 and ≥3 years); however, the model with only two classes (1 and ≥2 years) was competitive and particularly useful for monitoring because these two age classes can reliably be determined by direct observation in the field. Among yearlings, 77.4% were fecund and 11.7% twinned, whereas among older females 94.6% were fecund and 72.6% twinned. At a population level, annual variation in age structure (proportion ≥2 years) correlated well with annual variation in twinning rate except in the north-west Pre-Caspian population. Our results suggest that the recent poaching-driven collapse in saiga numbers has potentially resulted in reductions in fecundity, which will have an impact on population growth rate. Our results highlight the potential for monitoring of twinning rate using non-invasive calving aggregation transects as a cost-effective additional tool to population counts for monitoring the status of this critically endangered species. These monitoring methods are also potentially transferable to other ungulate species.     

Biology of the radiated shanny Ulvaria subbifurcata Storer in Newfoundland (Pisces: Stichaeidae)

Ulvaria subbifurcata is found on the north-east Atlantic coast of North America. Fish less than 55 mm preyed predominantly on copepods, while larger ones ate mainly nereids; polynoids and amphipods were eaten by all sizes. These four food items comprised the main food of the radiated shanny. Spawning occurred in May with the fish first spawning at age three to five. No conspicuous secondary sexual characters were observed. Females spawned once per year, producing a demersal egg mass. Males spawned up to four times and tended the egg mass (or masses). Incubation lasted 35–40 days, and the pelagic larvae settles on the bottom by August. Adult males tended to be larger than females of the same age but little difference was found sexually in the length–weight relationships. Ulvaria subbifurcata larger than 60 mm are nocturnal. This may reduce predation by, and competition with, other inshore benthic fishes.     

Reproduction, age and growth of Sillago maculata in south-eastern Australia

Sillago maculata is endemic to the east coast of Australia where it is harvested by recreational and commercial fishers; however, little is known of the important aspects of its biology and ecology to assist with fisheries management planning. This situation is redressed here by investigating aspects of the reproduction, age and growth of estuarine populations of S. maculata in south-eastern Australia. Gonadosomatic index (GSI) values indicated peak spawning occurred between September and February and that the estimated mean fork length at maturity (L₅₀) was 14.6 cm for males and 15.2 cm for females. Females displayed an asynchronous pattern of oocyte development, with individuals probably spawning multiple times in a spawning season. A validated aging protocol using thin sectioned otoliths was used to estimate the age of fish. The maximum ages for males and females were 9.5 and 12.0 years, respectively. Growth differed between sexes, with males ( L ∞ = 24.04, K  = 0.70, t ₀ = −0.09) attaining a smaller maximum length than females ( L ∞ = 25.01, K  = 0.72, t ₀ = −0.04). The age composition of gill-net and beach-seine samples mainly consisted of individuals aged 2–4 years, and there was evidence of variable recruitment. Management implications are also discussed.     

Female‐biased migration of stream‐dwelling Dolly Varden in the Shiisorapuchi River, Hokkaido, Japan

The first evidence for female‐biased migration in a partially migratory stream‐dwelling salmonid the Dolly Varden Salvelinus malma , a phenomenon well known in sea‐run and lake‐run populations, is presented. Dolly Varden in the Shiisorapuchi River in central Hokkaido, Japan, used both tributaries, of which there are many, and the main stem, but spawned only in tributaries. The size structures of Dolly Varden (≥age 1 + years) in tributaries were unimodal (<100 mm fork length, L _F) during non‐spawning seasons but changed to bimodal during spawning seasons (lower mode <110 mm, upper mode >120 mm L _F). Mature individuals were observed in both modal groups. From the trapping and census data, the small group appeared to be tributary resident and the large group main stem migrant. Males were common in both resident and migrant components. Most females, however, migrated to the main stem to mature, indicating female‐biased migration.     

Effects of maternal age and condition on parturition and the perinatal period of Antarctic fur seals

The effect of maternal age and condition on the date of parturition and the duration of the perinatal period of Antarctic fur seals at Bird Island, South Georgia, were investigated over three consecutive breeding seasons. Females rear young during a four-month lactation period in a highly seasonal but predictable environment. Although females may first pup at three years of age, they did not attain full adult size until six years of age; older females (≥ 6 years) tended to be heavier, longer, and in better condition than younger females (3–5 years). Older females returned to breeding beaches earlier and could occupy the most suitable pupping sites, and gave birth when densities of animals on the beaches were low (i.e. more favourable for pup survival). Females that arrived earlier were able to remain ashore longer with their pups prior to departing on their first foraging trips but this was unrelated to either maternal age or condition. Younger females returned later in the pupping season, possibly as a result of late implantation due to smaller energy reserves than older and larger females. In 1990 all females arrived late, were in poorer condition, gave birth to lighter pups, and had shorter perinatal periods. This suggests that not only was implantation late but that females returned to an area of low food availability prior to parturition.