Mackerel icefish size and age differences and long‐term change at South Georgia and Shag Rocks

This study analysed the total length ( L _T)‐frequency distribution of mackerel icefish Champsocephalus gunnari at South Georgia and Shag Rocks from nine bottom trawl surveys at South Georgia and eight at Shag Rocks between 1987 and 2002. The estimated mean L _T of age‐classes 1+, 2+, 3+ and 4+ years during January were, respectively, 14·7, 23·5, 29·8 and 35·1 cm at South Georgia. Age‐classes 1+, 2+ and 3+ years were 18·3, 26·2 and 33·8 cm at Shag Rocks. The derived Bertalanffy growth parameters for South Georgia were: L _∞ = 51·7 cm, k  = 0·27 and t ₀ = −0·26. The mean L _T of each age‐class of C. gunnari at Shag Rocks was significantly larger than at South Georgia, equivalent to c . 5 months growth, although the annual growth in L _T was similar. This is further evidence that C. gunnari hatched earlier at Shag Rocks. At South Georgia, the mean L _T of age‐classes 1+ and 3+ years were correlated, and significantly decreased between 1987 and 2002, and were smaller following warmer summers. This decrease in the size of C. gunnari may be the result of reduced food availability linked to climate warming.     

The reproduction, age and growth of the spotted rockling

Biology of the Macaronesian endemic rockling Gaidropsarus guttatus was studied in the Azores. The overall sex ratio from the samples was highly in favour of females (1 : 6·33). The growth parameters were L _∞ = 24·23, k  = 1·219 and t ₀ = −0·059. Fish matured at 15 cm L _T and the spawning season was strongly clustered in April.     

Age and growth of Anguilla anguilla in the Camargue lagoons

Age and total length ( L _T) data from a 11 year monitoring of the Anguilla anguilla eel population of the Camargue lagoons (Rhône delta, southern France) were collected for glass, yellow and silver eels. Three distinct models were calibrated to describe the growth process of undifferentiated eels, females and males, respectively. Uncertainty of parameter estimates was evaluated by bootstrapping. Females were characterized by larger asymptotic body size ( L _T) than males (580 ± 50 v . 388 ± 13 mm) and faster growth, whilst the Brody growth coefficient was larger for males than for females (means ±  s . d . 3·00 10⁻³ ± 1·68 10⁻³ v . 1·73 10⁻³ ± 0·50 10⁻³). Sexual differentiation was estimated to begin at 204 ± 38 mm mean ±  s . d ., i.e . at the end of the second year in the lagoons, well before the L _T at which macroscopic differentiation became possible ( c . 300 mm). Males probably leave the lagoon or die (due to either natural or fishing mortality) within the first 3 years, whilst females can remain up to 5 years. Sexual differentiation and maturation have a major role in shaping the L _T structure of the population. The L _T and mass ( M ) data were fitted by allometric curves     . The calibration of distinct curves for data from different years indicated that the allometric coefficient a was subject to wider interannual fluctuations than the allometric exponent b . A negative correlation linked the average L _T and the allometric exponent ( r  = −0·58, P  < 0·01).     

Population variables and life-history characteristics of the alligator pipefish Syngnathoides biaculeatus, in Papua New Guinea

Population structure and life-history variables of the widely distributed alligator pipefish Syngnathoides biaculeatus were characterized in Bootless Bay, Papua New Guinea over the course of 11 months. There was little evidence of seasonality with four focal populations showing no significant change in abundance. Similarly, the sex ratio remained 1:1 for all but 1 month. Reproductive males carrying eggs (148–278 mm in total length, L _T) were found in all months. Brood size was significantly, positively related to male L _T for newly laid broods only. Maximum observed brood size was 351 and mean ± s . d . brood size was 238 ± 57 for newly laid broods. Juveniles and males showed no change in mean L _T over the year while slightly smaller females were captured in November 2006 and September 2007. Males were significantly longer than females so von Bertalanffy growth coefficients were estimated separately for each sex: males L _∞= 285 mm, K = 0·82 year⁻¹ and females L _∞= 261 mm, K = 1·10 year⁻¹. These estimates suggest that this species grows rapidly and has a short-life span. In the context of growing concern about overexploitation of syngnathids, a rapid growth rate combined with year round reproductive activity suggests that the tropical S. biaculeatus may be relatively resilient with regard to fishing pressure.     

Age, growth and feeding of the common stingray (Dasyatis pastinaca, L., 1758) in the Cilician coastal basin, northeastern Mediterranean Sea

Growth and feeding of stingray ( Dasyatis pastinaca ) were studied using 346 specimens from the Cilician Basin coastal area (northeastern Mediterranean). Age classes between 0 to XII were found. The total length of all specimens ranged from 14.6 to 100.9 cm, and total weight was between 22.5 and 6800 g. Total length (TL)-weight (W) and disc width (DW)-weight (W) relationships were W = 0.0033*L^3.1429 and W = 0.0039*DW^3.4914, respectively. The age data, derived from central readings, were used to estimate the von Bertalanffy length and weight growth parameters. The results were L_∞ = 294.9 cm, W_∞ = 198690.1 g, K = 0.029 year⁻¹; t₀ = −2.2 year. The D. pastinaca diet was composed mainly of crustaceans.     

Age, growth, sexual maturity and food composition of Sciaena umbra in the south-eastern Black Sea, Turkey

Studied were the age, growth, maturity and food composition of the brown meager, Sciaena umbra, caught off Trabzon, south-eastern Black Sea (Turkey) in 2002–2003. A total of 329 individuals was collected by spear fishing and hand nets. The thin sectioning method was used for aging the fish otoliths. Fitted von Bertalanffy growth parameters for all fish were: L _∞ = 51.14 (±1.19) cm, k  =   0.27 (±0.02) year⁻¹ and t ₀ = −0.93 (±0.07) year. This study revealed that S. umbra is a relatively slow-growing and long-lived species with a life span in excess of 18 years. Sexual maturity begins when they reach a length of about 15 cm. Lengths at which 50% of brown meagre become mature are 19.50 for males and about 22 cm for females. Spawning begins in June, when the temperature is approximately 18°C, and ends in August. Gut content analysis indicated that this species feeds mainly on crustaceans, then switches to fish as they grow. Sciaena umbra appears to be an apex predator in the upper littoral zone.     

Population structure, growth, mortality and estimated stock size of the introduced tench, Tinca tinca (L.), population in Lake Beyşehir, Turkey

Population structure, growth, length–weight relationship, mortality and stock size of tench, Tinca tinca (L.), was studied in Lake Beyşehir, Turkey in 2005. Totals of 3360 tench (1865 males; 1795 females) were captured with gill- and trammel-nets of various mesh sizes. Male to female ratio was 1.04 : 1. The study covered length year classes. Fork lengths and total weights ranged from 9 to 37 cm and 13 to 815 g. For all individuals, the von Bertalanffy growth equation and length–weight relationship were L _t = 54.2[1−exp(−0.1350( t  + 1.0281)] and W  = 0.0151  L ^2.9993, respectively. Growth performance index and mean condition factor of the tench population were 2.598 and 1.513, respectively. Mortality rates were Z  = 1.97 year⁻¹, M  = 0.29 year⁻¹ and F  = 1.68 year⁻¹ for total, natural, and fishing mortality, respectively. The exploitation rate was E  = 0.85, and the percentage of surviving fish was 13.9%. Tench stock was assessed as about 6–7 million individuals and 1450–1500 tonnes in biomass. It was determined that maximum sustainable yield could be obtained with an 80% level of the current fishing effort.     

Age, growth and reproduction of the black scorpionfish, Scorpaena porcus (Pisces, Scorpaenidae), on the Black Sea coast of Turkey

Age, growth and reproduction of the black scorpionfish, Scorpaena porcus were studied in specimens from the coast of the Sinop Peninsula (Black Sea) between March 2002 and April 2003 in order to characterize these population parameters in comparison to specimens from populations of nearby regions. A total of 1086 specimens was captured by beam trawl at the depths between 0 and 30 m. The total number of females (510) was significantly higher than that of males (373). Total length of males and females ranged between 5.7 and 23.6 cm, and 4.9 and 31.7 cm, respectively. The length–weight relationship showed a positive allometric growth. Females grew faster and reached a larger size at age than males ( L _∞ = 111.9 cm, K  = 0.035 year⁻¹, φ' = 2.64 for females, and L _∞ = 74.6 cm, K  = 0.054 year⁻¹, φ' = 2.49 for males). The age range estimated was up to 8 years for females and 5 years for males. Reproduction likely occurs between June and September. Sex ratio varied greatly with season, perhaps indicating different seasonal migratory patterns in adults of different sex. An inverse correlation between gonadosomatic index (GSI) and hepatosomatic index (HSI) was evident during the reproduction seasons. The mean size at first sexual maturity was 17.5 cm TL for females, and 16.7 cm TL for males.     

Prey consumption rates and growth of piscivorous brown trout in a subarctic watercourse

Prey consumption rates of piscivorous brown trout Salmo trutta were studied in the Pasvik watercourse, which forms the border between Norway and Russia. Estimates of food consumption in the field were similar to or slightly less than maximum values from a bioenergetic model. The piscivore diet consisted mainly of vendace Coregonus albula with a smaller number of whitefish Coregonus lavaretus . Individual brown trout had an estimated mean daily intake of c . 1·5 vendace and 0·4 whitefish, and a rapid annual growth increment of 7–8 cm year⁻¹. The total population of brown trout >25 cm total length was estimated as 8445 individuals (0·6 individuals ha⁻¹), giving a mean ±  s . e . annual consumption of 1553880 ± 405360 vendace and 439140 ± 287130 whitefish for the whole watercourse. The rapid growth in summer of brown trout >25 cm indicated a high prey consumption rate.     

Age, growth, mortality and population structure of the oyster, Crassostrea madrasensis, in the Moheskhali Channel (southeastern coast of Bangladesh)

The population structure, age, growth, mortality and harvest intensity of the oyster Crassostrea madrasensis were examined in the Moheskhali Channel, Bangladesh between June 2003 and May 2004. The channel is a representative habitat for the area. C. madrasensis monthly length frequency data were analyzed using FiSAT software for estimating population parameters, including asymptotic length ( L _∝ ), growth co-efficient ( K ) and recruitment pattern to assess the status of the stock. Asymptotic length ( L∝ ) and growth co-efficient ( K ) were 20.88 cm and 0.35 year⁻¹, respectively. The growth performance index (φ') was calculated with 2.18. The growth pattern showed negative allometric growth ( b  < 3), with an asymptotic weight ( W _∝ ) of about 1124.6 g. The oyster attained an average length of 6.17 cm at the end of 1 year. Total mortality ( Z ) by length-converted catch curve was estimated at 1.78 year⁻¹, fishing mortality ( F ) at 0.77 year⁻¹, and natural mortality ( M ) at 1.01 year⁻¹. The exploitation level ( E ) of C. madrasensis was 0.43, while the maximum allowable limit of exploitation ( E _max) was 0.45 for the highest yield. The recruitment pattern was continuous, displaying a single major peak event per year. Habitat temperatures were 25.5–31.0°C (mean ± SD, 29 ± 1.62°C); salinity range was from 12.36 to 26.0 ppt (mean ± SD, 19.6 ± 4.7 ppt). The exploitation level (0.43) indicated that the oyster stock was exploited at almost maximum yield in this channel.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Endurance swimming of European eel

A long‐term swim trial was performed with five female silver eels Anguilla anguilla of 0·8–1·0 kg ( c . 80 cm total length, L _T) swimming at 0·5 body lengths (BL) s⁻¹, corresponding to the mean swimming speed during spawning migration. The design of the Blazka‐type swim tunnel was significantly improved, and for the first time the flow pattern of a swim tunnel for fish was evaluated with the Laser‐Doppler method. The velocity profile over three different cross‐sections was determined. It was observed that 80% of the water velocity drop‐off occurred over a boundary layer of 20 mm. Therefore, swim velocity errors were negligible as the eels always swam outside this layer. The fish were able to swim continuously day and night during a period of 3 months in the swim tunnel through which fresh water at 19° C was passed. The oxygen consumption rates remained stable at 36·9 ± 2·9 mg O₂ kg⁻¹ h⁻¹ over the 3 months swimming period for all tested eels. The mean cost of transportation was 28·2 mg O₂ kg⁻¹ km⁻¹. From the total energy consumption the calculated decline in fat content was 30%. When extrapolating to 6000 km this would have been 60%, leaving only 40% of the total energy reserves for reproduction after arriving at the spawning site. Therefore low cost of transport combined with high fat content are crucial for the capacity of the eel to cross the Atlantic Ocean and reproduce.     

Swimming performance and metabolism of 0+ year Thymallus arcticus

The prolonged swimming speed and metabolic rate of 0+ year Arctic grayling Thymallus articus were examined with respect to current velocity, water temperature and fish size, and compared to conditions fish occupy in the river. Oxygen consumption (mg O₂ h⁻¹) increased with fish mass and temperature (6–23° C), with a steep increase in metabolic rate between 12 and 16° C. Absolute prolonged swimming speed (cm s⁻¹) increased rapidly with fish size (total length, L _T, and mass), however, fish in the natural stream habitat occupied current velocities between 15 and 25 cm s⁻¹ or 4  L _T s⁻¹, approximately half their potential prolonged swimming speed (10  L _T s⁻¹).     

Sexual and geographical variation in life history parameters of the shorthorn sculpin

A total of 293 shorthorn sculpins Myoxocephalus scorpius from Tromsø, northern Norway, were sampled between November 1998 and April 1999 to determine sex, total length, age, growth, maturity and mortality. Females grew to larger sizes ( L _∞=26·9 v. 18·5 cm), matured later (2 v. 1 year of age) at larger size (maturation length=16 v. 14 cm L _T), and had lower instantaneous mortality rates (0·93 v. 1·20 year⁻¹) than males. The life history parameters of shorthorn sculpins in northern Norway were more similar to the parameters of short-lived central European populations than to the parameters of the long-lived population of Newfoundland. This study confirms that northern Norwegian shorthorn sculpins exhibit sexual dimorphism as in other shorthorn sculpin populations. The relationships between growth pattern, age at maturity and mortality rates observed in the Tromsø population and in other shorthorn sculpin populations, correspond well with the predictions from a published life history model.     

Growth and reproduction of Mesopotamian spiny eel (Mastacembelus mastacembelus Banks & Solander, 1794) in Ataturk Dam Lake (Şanliurfa), Turkey

Age at length, growth and reproduction of 220 Mastacembelus mastacembelus specimens from the Atatürk Dam Lake were studied from July 2005 to July 2006. Total lengths and weights ranged from 7.0 to 85.0 cm and from 6 to 1100 g, respectively. Maximum age was 13 years. The regression model fitted to length and weight data was W  =   0.0228  L ^2.43 for males and W  =   0.0029  L ^2.95 for females. The von Bertalaffy growth equations for males and females were L _t  = 99.2 [1−e^{−0.11 ( t −0.12)}] and L _t  = 69.2 [1−e^{−0.26 ( t −0.35)}], respectively. Males dominated especially at an older age; the overall sex ratio was 1 : 0.63 (M:F). The breeding period was from May to July. Fecundity ranged from 2540 to 24 000 eggs per female.     

On the life history of the lesser gurnard (Scorpaeniformes: Triglidae) inhabiting the Agulhas Bank, South Africa

Growth analysis based on sectioned sagittal otoliths revealed the lesser gurnard Chelidonichthys queketti on the Agulhas Bank to be relatively fast growing and long lived, with ages of up to 7 years being recorded. Total length at age (mm) was described best by the specialized von Bertalanffy growth model as L _T=306·1 (1 − e^{0·53(t+0·18)}). First approximations of total, natural and fishing mortality rates were determined at 0·73, 0·38 and 0·35 year⁻¹ respectively. The adult population was male dominated with a sex ratio of 1 female: 1·2 males with the mean size of males and females being similar. The lesser gurnard is an iteroparous species with females maturing by the end of the first year of life (195 mm L _T), thereafter spawning throughout the year with reproductive activity peaking over spring and late summer. The lesser gurnard appears to exhibit similar life-history patterns to other triglid species in that it can be classified as a generalist. Generalistic life-history characteristics such as a fast growth rate, early sexual maturity at a relatively large size, a non-seasonal spawning pattern, feeding on a variety of prey organisms and the ability to inhabit various substrata could all contribute to it maintaining a high biomass on the Agulhas Bank.     

Effects of temperature, body size and feeding on rates of metabolism in young‐of‐the‐year haddock

The mean rate of oxygen consumption (routine respiration rate, R _R, mg O₂ fish⁻¹ h⁻¹), measured for individual or small groups of haddock Melanogrammus aeglefinus (3–12 cm standard length, L _S) maintained for 5 days within flow‐through respiratory chambers at four different temperatures, increased with increasing dry mass ( M _D). The relationship between R _R and M _D was allometric ( R _R = α  M ^b ) with b values of 0·631, 0·606, 0·655 and 0·650 at 5·0, 8·0, 12·0 and 15·0° C, respectively. The effect of temperature ( T ) and M _D on mean R _R was described by     indicating a Q ₁₀ of 2·27 between 5 and 15° C. Juvenile haddock routine metabolic scope, calculated as the ratio of the mean of highest and lowest deciles of R _R measured in each chamber, significantly decreased with temperature such that the routine scope at 15° C was half that at 5° C. The cost of feeding ( R _SDA) was c . 3% of consumed food energy, a value half that found for larger gadoid juveniles and adults.     

Growth, diet and metabolism of common wolf–fish in the North Sea, a fast–growing population

The von Bertalanffy growth parameters for common wolf–fish Anarhichas lupus in the North Sea were: male: L ∞=111·2 cm, t ₀=–0·43 and K =0·12; and female: L ∞=115·1 cm, t ₀=–0·39 and K =0·11, making this the fastest growing stock reported. Resting metabolic rates (RMR±S.E.) and maximum metabolic rates (MMR±S.E.) for six adult common wolf–fish (mean weight, 1·39 kg) at 5° C were 12·18±1·6 mg O₂ kg^–1 h^–1 and 70·65±7·63 mg O₂ kg^–1 h^–1 respectively, and at 10° C were 25·43±1·31 mg O₂ kg^–1 h^–1 and 113·84±16·26 mg O₂ kg^–1 h^–1. Absolute metabolic scope was 53% greater at 10° C than at 5° C. The diet was dominated by Decapoda (39% overall by relative occurrence), Bivalvia (20%) and Gastropoda (12%). Sea urchins, typically of low energy value, occupied only 7% of the diet. The fast growth probably resulted from summer temperatures approximating to the optimum for food processing and growth, but may have been influenced by diet, and reduced competition following high fishing intensity.     

Growth and reproduction of the wedge clam (Donax trunculus) in the Sea of Marmara, Turkey

Reproduction, growth and mortality of the wedge clam Donax trunculus were studied in an unexploited population in the northern part of the Sea of Marmara. Age determination was based from counting shell increments by inspection of both the external ring structure and the internal structure on thin cross-sections of the shell. Maximum life span was observed as 6 years for the studied population, but 4 years (shell length 40–41 mm) were usually not exceeded. Maximum length was 44.8 mm. Growth parameters were estimated as L _∞   = 44.15 mm, k  =   0.62 year⁻¹, C  = 1 and WP = 0.83 from external ring structure, and L _∞   = 42.44 mm, k  =   0.75 year⁻¹, C  = 1 and WP = 0.79 from internal growth bands (thin section). Natural mortality ( M ) was estimated as 0.98 year⁻¹. Sex ratio was not significantly different from 1 : 1. The monthly maturation process was assessed macroscopically and from variation in the mean total ash-free dry weight per shell weight of adult individuals. Spawning occurred between April and July with a peak between May and June. The recruitment pattern was unimodal.     

The biology of the bigeye grenadier at South Georgia

The biology of the bigeye grenadier Macrourus holotrachys caught as by‐catch in the Patagonian toothfish Dissostichus eleginoides longline fishery conducted around South Georgia was investigated to improve data available for fisheries management. Age estimates suggest that M. holotrachys is a moderately slow growing species ( K  = 0·10), reaching ages of >30 years and attaining total lengths ( L _T) >80 cm ( L _∞ = 33). The size at which 50% of females had started to mature ( L _int50) for M. holotrachys was 21 cm pre‐anal length ( L _PA) and occurred at c . 9 years old. Estimates of natural mortality and Pauly's growth performance index were found to be low ( M  = 0·09 and Φ = 2·82 respectively). Gonad maturity stage was described from macroscopic and histological investigation. Mature ovaries had oocytes at all developmental stages with between 22 and 55% likely to be spawned each year. Absolute fecundity ranged from 22 000 to 260 000 eggs and was positively correlated with both pre‐anal length and mass. A highly skewed sex ratio of 32 : 1, females : males, was found for specimens caught by longlines but not for a small sample of shallower trawl‐caught specimens. It is suggested that females are far more susceptible to longline capture than males. Macrourus holotrachys is a bentho‐pelagic predator and scavenger that feeds on a wide range of fishes and invertebrates. The fish are long lived, slow‐growing species typical of deep‐water grenadiers; fisheries management strategies should reflect their probable susceptibility to overfishing.