Mercury in the marine food chain in the Southern Ocean at Macquarie Island: an analysis of a top predator,Patagonian toothfish (<Emphasis Type="Italic">Dissostichus eleginoides</Emphasis>) and a mid-trophic species,the warty squid (<Emphasis Type="Italic">Moroteuthis ingens</Emphasis>)

The characteristics and habitat of the Patagonian toothfish (Dissostichus eleginoides) are typical of fish that accumulate high concentrations of mercury. In this study, mercury determinations were made on samples of muscle tissue from Macquarie Island toothfish and the Southern Ocean deepwater warty squid (Moroteuthis ingens). The analysis of mercury in the biological tissues was made by cold vapour-atomic absorption spectrometry following acid digestion. Performance of the analytical procedure was assessed by analysis of certified reference material (DORM-2, dogfish muscle). Mercury concentrations of 16 Macquarie Island toothfish ranged from 0.12 mg kg^–1 (550 g, 381 mm TL) to 0.59 mg kg^–1 (6,100 g, 823 mm TL), with a mean concentration of 0.33±0.12 mg kg^–1. A significant correlation was found between mercury and either toothfish weight or total length. The fish analysed were juveniles, which suggests that larger individuals would have higher mercury concentrations well exceeding food standard code limits for mercury in fish (typically 0.5 mg kg^–1). Warty squid, also from around Macquarie Island, had a low mean mercury concentration of 0.086 mg kg^–1 in mantle tissue; no significant correlation existed between mercury concentration and either squid mantle length or total weight. It is postulated that the squid have a mechanism, possibly involving the digestive gland, that prevents bioaccumulation of mercury in the mantle, and presumably other body tissues.     

Growth and age structure of the swan mussel Anodonta cygnea (L.) at different depths in lake Mattsee (Salzburg, Austria)

Unionid clams were collected at 1–2 m, 3–4 m and 6–7 m depth in lake Mattsee, a moderately mesotrophic lake, to investigate the effect of depth on clam growth and age structure. No significant differences in age structure of Anodonta cygnea were found (p=0.65). Three and ten years old clams were present at all depths, but in different percentages. Whereas at 1–2 m 13.3% of the collected clams were <4 years old, this percentage was 4.4% at 6–7 m and 7.1% at 3–4 m. A greater percentage (6.7%) of older mussels (9, 10 years) were collected at 6–7 m than at 1–2 m (2.2%). Growth declined with depth. Total length at a given age of clams at 1–2 m and 3–4 m did not differ (p=0.54), whereas differences were significant between clams at 1–2 m and 6–7 m (p<0.05) as well as between 3–4 m and 6–7 m (p<0.05). The Growth constant k was highest at 1–2 m depth.     

Comparison of foraging strategies of incubating king penguins Aptenodytes patagonicus from Macquarie and Heard islands

The foraging strategies of king penguins from Heard and Macquarie islands were compared using satellite telemetry, time-depth recorders and diet samples. Trip durations were 16.8±3.6 days and 14.8±4.1 days at Macquarie and Heard islands, respectively. At Macquarie Island, total distances travelled were 1281±203 km compared to 1425±516 km at Heard Island. The total time the penguins spent at sea was 393±66 h at Macquarie Island and 369±108 h at Heard Island. The penguins from Macquarie Island performed more deep dives than those from Heard Island. King penguins from Macquarie Island travelled 1.5±0.2 km h⁻¹ day⁻¹ compared to 1.3±0.1 km h⁻¹ day⁻¹. At Macquarie Island, 19% of dives were upto 70–90 m depth compared to 35% at Heard Island. The main dietary prey species were the fish Krefftychthis anderssoni and the squid Moroteuthis ingens in both groups. The differences in the at-sea distribution and the foraging behaviour of the two groups of penguins were possibly related to differences in oceanography and bathymetric conditions around the two islands. Dietary differences may be due to interannual variability in prey availability since the two colonies were studied during incubation but in different years.     

Effects of temperature on growth rates of fungi from subantarctic Macquarie Island and Casey,Antarctica

Summary The linear growth rates of fungal isolates were measured on agar plates at temperatures ranging from 4° to 35°C. Fungi tested included the major fungal colonizers of leaves and litter of the three dominant plant species on subantarctic Macquarie Island, and major fungal species associated with plant and soil communities near Australia's Casey Station on the Antarctic Continent. All fungi grew at 4°C and were classified as psychrotrophs. Maximum growth rates were recorded at temperatures of 10° to 20°C for 13 of the 15 isolates from Macquarie Island and for all six isolates from Casey. Most of the leaf colonizing fungi from Macquarie Island had optimum growth temperatures of 15°C whereas all litter fungi from Macquarie Island and Casey fungi except Thelebolus microsporus had optimum growth temperatures of 20°C or above. Maximum growth of all species was at temperatures above those normally prevailing in their natural environments, with most species growing at 4°C at between 10% and 30% of their maximum rates. However, microclimatic effects may have resulted at times in temperatures near their growth optima. The highest growth rates at 4°C were recorded for Phoma spp. 1 and 2, Phoma exigua and Mortierella gamsii from Macquarie Island and Mortierella sp. 1 from Casey. Thelebolus microsporus and sterile sp. G from Casey also grew relatively fast at 4°C, and these species, and Phoma sp. 3 and Phoma exigua from Macquarie Island had the lowest Q-₁₀ values for the temperature range 4° to 15°C.     

Age and growth estimates of the bull shark,Carcharhinus leucas,from the northern Gulf of Mexico

Synopsis Length at age and growth rates for 59 bull sharks, Carcharhinus leucas, collected from the northern Gulf of Mexico were estimated from the band patterns formed seasonally in the vertebral centra. The combined age at length data for both sexes were applied to a von Bertalanffy growth model producing parameter estimates of L = 285 cm TL, K = .076, t₀ = –3.0 yr. Lengths at age for males and females were similar except that males did not attain as great a length as females. Growth was apparently slow and varied among individuals, but in general, was estimated to be 15–20 cm yr^–1 for the first five years, 10 cm yr^–1 for years 6–10, 5–7 cm yr^–1 for years 11–16, and less than 4–5 cm yr^–1 thereafter. Males mature at 210–220 cm TL or 14–15 yr of age; females mature at>225 cm TL or 18+ yr of age. The largest male (245 cm TL) was 21.3 yr old; the largest female (268 cm TL) was 24.2 yr old.     

Axial rod growth and age estimation of the sea pen,Halipteris willemoesi Kölliker

Halipteris willemoesi is a large octocoral commonly found in the Bering Sea. It is a member of a ubiquitous group of benthic cnidarians called sea pens (Octocorallia: Pennatulacea). Sea pens have a skeletal structure, the axial rod, that in cross section exhibits growth rings. Pairs of adjacent rings, or ring couplets, were assumed to be annuli and were used to estimate the age and growth of H. willemoesi. Twelve axial rods, extracted from H. willemoesi collected in the Bering Sea, were selected to represent small (25–29 cm total length), medium (97–130 cm TL) and large (152–167 cm TL) colonies. Each rod resembled a tapered dowel; the thickest part (0.90–6.75 mm in diameter) was at about 5–10% of total length from the base tip, the distal part was more gradually tapered than was the base. The number of ring couplets increased with rod size indicating their utility in estimating age and growth. Estimated age among rods was based on couplet counts at the thickest part of each rod; the average estimated age (±SE) was 7.1 ±0.7, 19.3 ±0.5, and 44.3 ±2.0 yr for small, medium and large-size rods, respectively. Based on these estimated ages, average growth rate in total length was 3.9 ± 0.2, 6.1 ± 0.3, and 3.6 ± 0.1 cm yr^–1 for small, medium, and large-size colonies. The average annual increase in maximum rod diameter among all colonies was 0.145 ± 0.003 SE mm yr^–1; therefore, age prediction from maximum rod diameter was calculated (estimated age (yr) = 7.0 * (maximum rod diameter, mm) –0.2; R ² = 0.99). At maximum diameter, the average couplet width was relatively constant among the three colony sizes (0.072 ± 0.05 mm). X-ray diffraction and electron microprobe analyses revealed that the inorganic portion of the rod is composed of a high-magnesium calcite. Radiometric validation of these age and growth rate estimates was attempted, but high amounts of exogenous ²¹⁰Pb precluded using the disequilibria of ²¹⁰Pb:²²⁶Ra. Instead, ²¹⁰Pb activities were measured in a series of cores extracted along the axial rod. These activities ranged from 0.691 ± 0.036 (SE) to 2.76 ± 0.13 dpm g^–1, but there was no pattern of decay along the length of the rod; therefore, the growth rates and corresponding ages could not be validated. Based on estimated age from ring couplet counts, growth in total rod length is slow at first, fastest at medium size, and slows toward maximum size, with an estimated longevity approaching 50 yr.     

Belowground carbon storage of Micronesian mangrove forests

Belowground carbon storage was examined for mangrove forests on Pohnpei Island, Micronesia. Stored carbon in a coral reef-type mangrove habitat consisting of a 2 m thick mangrove peat layer, which is a type of mangrove habitat in tropical Pacific islands, was estimated at 1300 t C ha^–1. The carbon burial rate during the phase of gradual sea-level rise, which was calculated at 93 g m^–2 year^–1 between 1800 and 1380 years bp using the medians of the radiocarbon ages, was significantly higher than that between 1380 years bp and present in a stable sea-level phase.     

Age and growth of king and Spanish mackerel larvae and juveniles from the Gulf of Mexico and U.S. South Atlantic Bight

Synopsis Sagittal otoliths from 50 king mackerel 2.9–13.0 mm SL and 72 Spanish mackerel 2.8–22.0 mm SL collected off the southeast U.S. were examined whole at 400 × using a compound microscope-video system. Otoliths of both species had visible, presumably daily, growth increments as well as finer subdaily increments. Otolith growth was directly proportional to growth in standard length for king (r² = 0.91) and Spanish mackerel (r² = 0.86). Spanish mackerel were estimated to be 3–15 d old with a mean absolute growth rate (SL/number of growth increments) and 95% confidence interval of 1.15 ± 0.07 mm · d^–1. The least squares linear equation: SL = –1.30 + 1.31 (age in days), with r² = 0.67 and p < 0.001, described the relationship between length and age. There was a significant positive relationship between absolute growth rate and fish length. King mackerel were estimated to be 3–15 d old with a mean absolute growth rate of 0.89 ± 0.06 mm d^–1. The least squares linear equation: SL = 0.37 + 0.82 (age in days), with r² = 0.77 and p < 0.001, best described the relationship between length and age. The relationship between growth rate and fish length was not significant. The growth rate of king mackerel was slightly higher for fish from the Mississippi River plume than from all other locations combined, while Spanish mackerel growth rates were not significantly different.     

Consequences of depletion of stratospheric ozone for terrestrial Antarctic ecosystems: the response of Deschampsia antarctica to enhanced UV-B radiation in a controlled environment

Mini UV lamps were installed over antarctic plants at Léonie Island, Antarctic peninsula, and shoot length measurements of Deschampsia antarctica were performed during the austral summer January–February 1999.We studied the response of the antarctic hairgrass, Deschampsia antarctica to enhanced UV-B. In a climate room experiment we exposed tillers of Deschampsia antarctica, collected at Léonie Island, Antarctic peninsula, to ambient and enhanced levels of UV-B radiation. In this climate room experiment with 0, 2.5 and 5 kJ m^–2 day^–1 UV-B_BE treatments we observed that length growth of shoots at 2.5 and 5 kJ m^–2 day^–1 UV-B_BE was markedly reduced compared to 0 kJ m^–2 day^–1 UV-B_BE. In addition, there was an increased number of shoots and increased leaf thickness with enhanced UV-B. The Relative Growth Rate (RGR) was not affected by UV-B, possibly because reduced shoot length growth by enhanced UV-B was compensated by increased tillering. Light response curves of net leaf photosynthesis of plants exposed to 5 kJ m^–2 day^–1 UV-B_BE did not differ from those exposed to 0 kJ m^–2 day^–1 UV-B_BE. The content of UV-B absorbing compounds of plants exposed to increasing UV-B did not significantly change.Mini UV-B lamp systems were installed in the field, to expose the terrestrial antarctic vegetation at Léonie Island to enhanced solar UV-B. In that study, the increment of shoot length of tagged plants of Deschampsia antarctica during the January-February 1999 at Léonie Island, was recorded and compared to shoot length growth under controlled conditions.The consequences of enhanced UV-B radiation as a result of ozone depletion for the terrestrial antarctic ecosytems are discussed.     

A new method for measuring growth and age in the precious red coral<Emphasis Type="Italic"> Corallium rubrum</Emphasis> (L.)

A new technique for aging red coral Corallium rubrum (L.) colonies based on staining the organic matrix found in the axial calcareous skeleton is presented and validated. This method provided clear-cut images of growth rings of red coral. To demonstrate their annual periodicity, two approaches have been used: (i) applying this technique to adult colonies of known age (more than 20 years old), and (ii) labeling colonies with calcein and allowing them to grow for 1 year. Results provided evidence of the annual periodicity of growth rings. This new method assesses colony age with an underestimate of true age by 3–4 years. The difference between estimated age and actual age could be attributed to the phase of initial growth during which rings are not formed. Colonies from different sites, depths, and habitats (n=33) were analyzed yielding preliminary data on longevity and mean growth rates in red coral. Colonies from shallow habitats (15–62 m) examined here with basal diameter of about 7 mm were at least 30–40 years old. Mean growth rate of basal diameter was 0.35±0.15 mm year^–1. Comparison with previous aging methods used for red coral resulted in considerable differences in estimations of age (about 10 years greater in this study) and growth rates (about four times lower). The application of this method to red coral will provide key data as a basis for developing management and conservation plans for this valuable species.Communicated by: H.R. Lasker     

Age determination,growth and mortality of Gerres subfasciatus Cuvier, 1830 in southeast Australia

Commercial beach‐seine (30–50 mm cod‐end mesh) catches of Gerres subfasciatus in Lake Macquarie southeast Australia were sampled monthly between December 2000 and April 2002 to investigate species age, growth and mortality characteristics using sectioned sagittal otoliths. Inclusion of fishery‐independent length data of young‐of‐the year collected from littoral seagrass beds with fine meshed beach seines augmented growth analyses. Fifty otoliths each month (total 448 female and 402 male) were examined with sections displaying alternating opaque and translucent zonation. Formation of otolith opaque zones occurred annually between August and December as determined by monthly marginal increment analyses. Spawning occurred between October and February, and a universal birth date of 1 December was assigned that allowed counts of opaque zones to be converted to age estimates in years and months (decimal ages). The von Bertalanffy growth function identified that both genders grew fast for their initial 2 years, but thereafter slowed. Females grew faster, had a greater mean fork length‐at‐age, estimated L_∞ and an observed greater maximum fork length in samples compared to males. Nevertheless, observed longevity was 10⁺ years for both genders. Commercial catches of both genders were dominated by the 2⁺ and 3⁺ year age classes. Catch curve analyses identified the instantaneous rate of total annual mortality to be ~0.8 and an exploitation rate of <0.5 for both genders. The data form a basis for developing assessment and management strategies of G. subfasciatus fisheries.     

Fur seals at Macquarie Island: post-sealing colonisation,trends in abundance and hybridisation of three species

Commercial sealers exterminated the original fur seal population at Macquarie Island in the early 1800s. The first breeding record since the sealing era was not reported until March 1955. Three species of fur seal now occur at Macquarie Island, the Antarctic (Arctocephalus gazella), subantarctic (A. tropicalis) and New Zealand (A. forsteri) fur seal. Census data from 54 breeding seasons in the period 1954–2007 were used to estimate population status and growth for each species. Between the 1950s and 1970s, annual increases in pup production for the species aggregate were low. Between 1986 and 2007, pup production of Antarctic fur seals increased by about 8.8% per year and subantarctic fur seals by 6.8% per year. The New Zealand fur seal, although the most numerous fur seal species on Macquarie Island, has yet to establish a breeding population, due to the absence of reproductively mature females. Hybridisation among species is significant, but appears to be declining. The slow establishment and growth of fur seal populations on Macquarie Island appears to have been affected by its distance from major population centres and hence low immigration rates, asynchronous colonisation times of males and females of each species, and extensive hybridisation.     

Long distance migration of insects to a subantarctic island

Transoceanic migration of four species of macrolepidoptera to subantarctic Macquarie Island has been detected in 7 out of 33 years during the period 1962–96 and is restricted to spring and autumn. Analyses of synoptic charts during the migration period show that autumn immigrants originated from New Zealand and comprised a single species of noctuid moth,Agrotis ipsilon (Walker). Spring immigrants originated from Australia and comprised two noctuids, Dasypodia selenophora Guenée and Persectania ewingii Westwood and a butterfly, Vanessa kershawi (McCoy). Autumn migrations were associated with depressions in the southern Tasman Sea. Spring migrations were associated with the eastward passage of prefrontal airflows ahead of cold fronts which extended from southern Australia to the west of Macquarie Island. In an analysis of one of these events, winds exceeded 30 ms^?1 at 300 m altitude and could have transported migrants from Tasmania to Macquarie Island overnight in less than 10 h. Flight activity was assisted by the presence of a nocturnal temperature inversion that maintained upper air temperatures above 5 °C. The effect of potential global warming on the migration and colonization of Macquarie Island by insects is discussed.     

Abundance and distribution of a brown trout (Salmo trutta, L.) population in a remote high mountain lake

Brown trout (Salmo trutta) population of a remote high mountain lake (Lake Redó, Pyrenees, 2240 m above sea level) were studied during autumn using hydroacoustic techniques. This acoustic technique was for the first time used on fish at such high altitude in Spain. Sampling using multimesh nets fish catches and echosounding recording were carried out in September 1998. Mean density of fish was estimated to be 1.82 fish per 1000 m³ (597 fish ha^–1). The results exhibited mainly a littoral habitat, with the brown trout being preferentially in the 10–25 m deep layer, where the water was warmer and the richness and diversity of macroinvertebrates higher. The sampling by hydroacoustic technique found a length frequency range of fish higher than the multimesh gill nets but both of them estimated similar fish proportion for the common length range. The more frequent target strength (TS) for the population was –38 dB (TS range –37 to –39 dB). Good correlation was found between TS frequency distribution obtained by echosounding and that predicted by means of a model based on the log of the fish total length from multimesh gill nets captures.     

Production rates of Eurytemora affinis in the Elbe estuary,comparison of field and enclosure production estimates

Production rates of the calanoid copepod Eurytemora affinis were estimated from field studies in the Elbe estuary and from an enclosure experiment. As one basic parameter of production rates, the body length, was compared between both investigations. Most of the copepodid stages in the enclosure experiment reached a significant greater length than the copepodids in the estuary. The differences in length between copepods from the field and the experiment could mainly be explained by a four times higher chlorophyll-a level in the enclosure experiment. The better food supply also results in a higher individual growth rate for all instars in the enclosure experiment. Therefore the population of Eurytemora affinis in the Elbe estuary was regarded as food limited during certain times of the year, especially in late spring and summer.Maximum daily production rate in the enclosure experiment (40 µg dw l^–1 d^–1) was four times higher than in the estuary (12 µg dw l^–1 d^–1). The mean daily P:B ratio in the enclosure was 0.301 d^–1 compared to 0.11 d^–1 in the estuary.     

Growth, Natural Mortality, Length–weight Relationship, Maximum Length and Length-at-first-maturity of the Coelacanth Latimeria chalumnae

Based on the re-interpretation of published data, the von Bertalanffy growth function parameters of the coelacanth, Latimeria chalumnae, are estimated as L=218cm total length, s.e. 23; K=0.059 (year^–1), s.e. 0.012; t₀=–3.3 (year), s.e. 0.5, corresponding to a life span of 48 years. The length–weight relationship of the form W=a*TLb, with wet weight (W) in g and total length (TL) in cm, is estimated as a=0.0278, b=2.89, r²=0.893, n=87, range=42.5–183cm TL. Using extreme value theory, the maximum length for female coelacanths is estimated as 199cm TL (95% confidence interval=175–223cm TL) and for males as 168cm TL (95% confidence interval 155–180cm TL). Based on data from seven females with embryos or mature eggs, the length-at-first-maturity for females is estimated to be about 150cm TL, corresponding to an age of about 16 years. Based on the value of t₀=–3.3 years and on the presence of three scale rings found in a newborn coelacanth, the period of embryogenesis lasts for about three years, the longest known in vertebrates. The natural mortality rate is estimated at M=0.12. Population food consumption is found to be 1.4 times the existing biomass per year, and gross food conversion efficiency indicates that only 10% of the consumed food is utilized for somatic growth.     

Age and Growth of the Whiskery Shark, Furgaleus macki, from Southwestern Australia

Age and growth of the whiskery shark, Furgaleus macki, from southwestern Australia were examined using vertebral ageing and tag-recapture data. The readability of bands on the vertebral centra varied markedly between individuals. Four readers were used to make band counts, with the most experienced reader having the lowest index of average percent error and the highest level of agreement with final counts. Marginal increment analysis indicated that opaque bands form in January. With parturition occurring from August to October, size data suggests that the first band is probably formed 15–17 months after birth. The age at maturity was estimated to be 4.5 years for males, and 6.5 years for females. The oldest male was 10.5 years, and oldest female was 11.5 years. Von Bertalanffy growth parameters for males were L =121.5cm fork length, K=0.423 year^–1, t ₀=–0.472 years, were L =120.7cm fork length, K=0.369 year^–1, t ₀=–0.544 years for females, and were L =118.1cm fork length, K=0.420 year^–1, t ₀=–0.491 years for combined sexes. Data from a tag recapture study were analysed using a maximum likelihood method to verify the estimates of growth parameters from vertebral ageing. Von Bertalanffy growth parameters from the tag recapture study were L =128.2cm fork length, K=0.288 year^–1, t ₀=–0.654 years. The two methods of estimating growth parameters produced similar results, with rapid growth until approximately 5 years of age, after which there was little increase in length.     

Reproduction, population dynamics, growth and production ofScrobicularia plana da costa (pelecypoda) in the Bidasoa estuary, Spain

The breeding cycle, recruitment, population dynamics, growth and production ofScrobicularia plana were studied at one station in the Bidasoa estuary (SE of the Biscay Bay, Spain) during a period of 3 or 4 years. To complete this study, the reproduction for a period of 1 year was analysed at two other sites of the estuary. At none of the stations important differences in spawning activity were observed between the different years. The animals reproduced for the first time when they reached the age of two years. The histological data and the recruitment analysis showed only one spawning period between June and mid-September, with a peak in July-August. This breeding pattern differs from those shown by other southern European populations. The recruitment of spat (0.25–0.50 mm) occurred from June–July to October–December in different years. The population showed different annual patterns of density and population structure, depending on recruitment success. Growth was most rapid in spring and summer. The bivalves reached a mean length of 21.8 mm at the age of approximately 16 months; in the following year they grew to 30 mm. The growth during the life span fitted the theoretical growth equation of Von Bertalanffy. Annual production was in the range of 59.0–83.4 g AFDW m^–2 year^–1. The P/B ratios of the population varied between 0.84 and 1.48 (1.06 ± 1.36; ¯x ± 95% C.I.).     

Use of space and food by resident and migrant brown trout,Salmo trutta

Synopsis Parr and resident forms of brown trout,Salmo trutta, from Vangsvatnet Lake, Norway live in freshwater, while migrant forms live in coastal waters during summer and in freshwater during winter. About 80% of parr and residents live at depths <5 m, smolts and migrants are more confined to near-surface water. Brown trout partly segregate by size, age and sex from spring through autumn. More than 90% of parr and residents in the tributaries are 0–2 years old, 2–14 cm in length, in the littoral zone 0–3 years old, 7–24 cm in length, and in the pelagic zone 2–6 years old, 18–32 cm in length. The mean body length of equal-aged fish increases from tributaries through littoral to pelagic zones in the lake. Smolts (2–7 years, 14–29 cm) leave the lake from April through August and return during September–October. Migrants (2–11 years, 23–67 cm) leave the take in April–May and return during August–September; sexually mature fish return earlier than immatures. Female brown trout are less stream-dwelling, but more migrant and pelagic than males. Most individuals in the lake population spend the winter in the littoral zone. In the tributaries, diet differs significantly between age-groups of parr; young fish feed on smaller food items than do older fish. In the lake, parr and residents living in the same habitats feed on the same food items. Littoral brown trout feed mainly on insect larvae and chironomid pupae, pelagic brown trout feed on zooplankton and surface insects. Migrants feed little while staying in freshwater, except for matures which feed on young salmonids and surface arthropods during the 2 first months after they had returned from coastal waters. The results are discussed in relation to growth possibilities and mortality risks of the different habitats.Reprint request to B. Jonsson.     

Studies on the age and growth of the bata,Labeo bata (Ham.) (Cyprinidae,Teleostei) from the river Kali,India

Age and growth of Labeo bata (Ham.) was studied by the analysis of annuli found on the scale and by length-frequency distribution. The fish attained lengths of 131, 194, 236, 277, 314, 341 and 364 mm at the end of the 1st, 2nd, 3rd, 4th, 5th, 6th and 7th years of life respectively. The increase in length of scale bears a constant relationship with the increase in length of fish, and regression analysis yielded a straight line between scale and body length. Calculated values could be expressed as: Y = –2.534 + 0.064 XThe growth rate of the fish was found high during the 1st and 2nd years and decreased gradually afterwards till the 7th year. Both sexes showed more a or less similar growth rate and attained a similar longevity. Growth trend of the fish confirmed the von Bertalanffy growth equation: Lt = 450(l–e^{–0.2165(t+0.5963))} The seasonal growth curve was chiefly influenced by feeding intensity in fishes of 1st year class while in adults it was affected by feeding intensity as well as by maturation of the gonads.