• Korean Journal of Ecology and Environment
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• v.43 no.1
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• pp.82-90
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• 2010

The ecological characteristics of the Korean Aucha perch, Coreoperca herzi, were determined in order to estimate stock of the mid-upper system of the Seomjin River. The age was determined by counting the otolith annuli. The oldest fish observed in this study was 5 years old. Relationships between body length (BL) and body weight (BW) were $BW=0.0195BL^{3.08}$ ($R^2=0.966$) (p<0.01). Relationships between the otolith radius (R) and body length (BL) were BL=3.882R+1.66 ($R^2=0.944$). The von Bertalanffy growth parameters estimated from a non-linear regression method were $L_{\infty}=19.68\;cm$, $W_{\infty}=188.64\;g$, $K=0.17\;year^{-1}$ and $t_0=-1.46$ year. Therefore, growth in length of the fish was expressed by the von Bertalanffy's growth equation as $L_t=19.68$ ($1-e^{-0.17(t+1.46)}$) ($R^2=0.997$). The annual survival rate (S) was estimated to be $0.666\;year^{-1}$. The instantaneous coefficient of natural mortality (M) of estimated from the Zhang and Megrey method was $0.346\;year^{-1}$, and instantaneous coefficient of fishing mortality (F) was calculated $0.061\;year^{-1}$. From the estimates of survival rate (S), the instantaneous coefficient of total mortality(Z) was estimated to be $0.407\;year^{-1}$.

• Journal of the Korean Society of Marine Environment & Safety
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• v.19 no.1
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• pp.9-16
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• 2013

The growth and production of Aulichthys japonicus (6.70~15.32 cm TL) were investigated in an eelgrass bed of Dongdae Bay, Korea throughout 2006. A total 888 A. japonicus were collected with a small beam trawl. Growth in fish total length was expressed by the von Bertalanffy's growth equation as: $L_t=24.8257(1-e^{-0.5583(t+0.4816)})$. The densities, biomass, daily, annual production, and P/B ratio were $0.01{\pm}0.009/m^{-2}$, $0.17{\pm}0.16g/m^2$, $0.00006{\pm}0.00006g$ AFDW/$m^2$/day, 0.02g AFDW/$m^2$/yr, and 0.12, respectively. Monthly variation in production of A. japonicus was large; the peak occurred at July, September and November 2006 (0.000182, 0.000127 and 0.000123 g AFDW/$m^2$/day), where as the lowest value was 0.000003g AFDW/$m^2$/day at April and May 2006. Monthly change in production of A. japonicus was positive correlated with number of individuals, biomass and growth rate.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.49 no.4
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• pp.499-508
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• 2016

We investigated regional differences in the growth and maturation rate of Pacific cod in the East and Yellow Seas. Significant regional differences were detected in the von Bertalanffy growth equation and mean length at maturity (L₅₀). Cod in the East Sea grew at a faster rate than those in the Yellow Sea, with females growing faster than males in both populations. Cod of both sexes matured earlier in the Yellow Sea (age of maturity: 2.3 years for males, 2.6 years for females) than in the East Sea (age of maturity: 3.9 years for males, 4 years for females). These regional differences suggest that Pacific cod in the Yellow Sea, which is at the southwestern extremity of global cod distribution and thus likely to be an inhospitable habitat for this species, have adapted to their environment by developing earlier maturation and slower growth than cod in the East Sea or the Korea Strait. These regional differences must be taken into account when setting biological reference points for management of the Pacific cod fishery in Korean waters.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.2 no.1
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• pp.21-30
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• 1997

The present study reports the density, growth and production of a razor clam, Sinollovacula constricta, which is known to be one of the important fishreies catches from the Korean tidal flat. The annual yield reached to about 6,000 metric tons per year till 1994. The study was conducted on the Hwaseong tidal flat located on the central west coast, 40 kilometers south-west from Seoul. The annual yield of the razor clam in this area reached to about 50% of the total catch from the whole Korean coast. Samples were colleted monthly at 14 occasions from May 1992 to August 1993. Density of S. constricta ranged from 92~165 individuals per square meter during the study period. General trend of decreasing density was observed when the animal became older, but an exception was the year class of 1991 whose density was lower than that of 1990. The size of the shell was clearly separated into two classes during fall and winter (from September to February), however, the maximum frequency of the length of small size classes moved to right after February. It indicates a fast growth of young clams from spring to summer. Fast growth of the shell could also be examined by the growth curve. The shell growth of the whole life span was described by the von Bertalanffy equation of $L_t=89.3{\times}[1{\exp}\{-0.58{\times}(t+0.73\}]$. The growth in flesh dry weight was well fitted to the Gompertz growth model with the equation, $W_t=5.00{\times}{\exp}\{-4.31{\times}{\exp}(-0.043{\times}t)\}$. The clam lost about 30% of the body weight during spawning in August. The annual production calculated based on the data from September 1992 to August 1993 amounted to 150 g $DW{\cdot}m^{-2}{\cdot}yr^{-1}$ which was 2~50 fold higher than those of other bivalves occurred in Korea. This estimate was patitioned by each year classes; 87.5 by 1992, 53.4 by 1991, 59.0 by 1990 and -30.0 g $DW{\cdot}m^{-2}{\cdot}yr^{-1}$ by 1989 year class.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.16 no.2
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• pp.82-87
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• 1983

The aging and growth of Spisula sachalinensis from Ingu over the period from December 1981 through November 1982 were studied. The rings on the shell were used as the character for age determination. The ring where the translucent zone shifts to the opaque one was regarded as an annulus. The time of its formation was estimated by monthly variations of marginal growth rate in the shell. It was formed once a year over the period from August through September. The shell length at the formation of the annulus was estimated by taking the mean shell length corresponding to each of the annual ring. From analysis of mean shell length at the formation of the annulus, von Bertalanffy's growth equation was estimated as follows; $l_t=126.38(1-e^{-0.262(t-0.656)})\;W_t=485.85(1-e^{-0.262(t-0.656)})^3$ Back-calculated shell lengths estimated from this equation was quite consistent with actual shell lengths.