• Korean Journal of Ichthyology
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• v.23 no.4
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• pp.269-277
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• 2011

Age and growth pattern of Pacific cod Gadus macrocephalus were determined using samples collected in Jinhae Bay in Korea during the spawning period from 2006 to 2009. The ages of 333 specimens were estimated using their otoliths. The reliability of scales as a means of age determination was analyzed by comparing the ages estimated from otoliths and scales of 96 specimens. The scales collected from the base of the second dorsal fin or from the caudal peduncle were proved to be suitable for age determination of Pacific cod. Monthly changes in the marginal index in otoliths decreased from December showing the lowest value in February. Ages ranged from 4 to 6 years for both females and males, and most of them were 6 years old. Relationships between the otolith radius (R) and total length (TL) were TL=10.4R+3.1 for males, and TL=11.5R+3.4 for females. The growth curves in total length ($L_t$, cm) were expressed as $L_t$=141.5 [1-exp{-0.089 (t+0.209)}] for males and $L_t$=127.5 [1-exp {-0.124 (t+0.077)}] for females.

• Development and Reproduction
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• v.20 no.4
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• pp.331-347
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• 2016

Sexual dimorphism is the most conspicuous difference between the sexes. This study examines possible sexual dimorphism and the relative growth patterns of morphometric characteristics in the marine medaka, Oryzias dancena for their potential to help differentiate between males and females of this species. The von Bertalanffy growth parameters estimated by a non-linear regression method were $L_{\infty}=30.2mm$, K=3.22/year, and ${\tau}_0=-0.05$. All 18 characteristics measured showed a difference between males and females from 70 days after hatching. Each of these characteristics were significantly different between sexes (ANCOVA, P<0.05), and the ratio of standard length between sexes showed that males were larger than females for all five morphometric measurements. Fin length measurements were taken for 21 distances of anal fin and 7 distances of dorsal fin between landmarks. There were all differences for all dorsal fin rays between the males and the females and there is significant difference in 70 days after their hatch when the sexual dimorphism is presented. The significant difference (P<0.05) in fin ray for male and female was more greatly seen as they grow. Male marine medaka showed more rapid growth than females, with longer length, dorsal fins and anal fins. Differences in these characteristics will be useful during experiments when it is necessary to differentiate between sexes of marine medaka.

• Journal of the Korean Society of Fisheries and Ocean Technology
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• v.53 no.4
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• pp.363-375
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• 2017

The age and growth of pointhead flounder, Hippoglossoides pinetorum caught by gill nets was analyzed in this study from March 2015 to July 2017. New annuli were formed in H. pinetorum otoliths annually, and the boundary was set between the opaque and translucent zones from March and April. The relationships between total length (TL) and body weight (BW) were $BW=0.0025TL^{3.409}$ ($r^2=0.9551$) for females and $BW=0.0057TL^{3.138}$ ($r^2=0.9163$) for males. In this study, the ring of pointhead flounder, H. pinetorum was formed between 3 and 8 for females and between 3 and 6 for males. Total length (TL) and otolith radius (OR) were measured as follows: TL = 7.142 OR + 0.769 ($r^2=0.793$) for females and TL = 6.498 OR + 1.706 ($r^2=0.652$) for males. The mean distances of first ring ($r_1$) were 0.92 mm and 0.91 mm for females and males respectively. The TLs at the time of annulus formation, back-calculated from the otolith-length relationship by reference to the von Bertalanffy growth curves, were $L_t=43.59(1-e^{-0.15(t+0.007)})$ for females and $L_t=28.13(1-e^{-0.26(t+0.006)})$ for males while the growth between female and male was different.

• Food Science of Animal Resources
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• v.28 no.2
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• pp.187-195
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• 2008

The purpose of this study was to establish proper shipping weight and backfat thickness by applying the growth model to backfat thickness, measured by means of not only body weight, but also ultrasonography, and predicting the changes by age. Three breeds, i.e. Duroc, Landrace, and Yorkshie, were analyzed, and the Gompertz, logistic, and Von Bertalanffy model were used for inference with the parameter of the growth model being sex. As a result, both body weight and backfat thickness showed different growth curve parameters and characteristics at inflection points depending on model selection and sex. As for backfat thickness, in estimating the inflection point, unlike the case of body weight, the inflection ages of the boars of the Duroc breed was earlier than that of sows, whereas the inflection ages of the sows of the Landrace and Yorkshire breeds was earlier than that of boars. More than anything else, in the analysis of the changes in backfat thickness according to body weight, as the body weight reached 145kg, the backfat thickness showed much variation as great as 1.7-3.2 cm in each breed and sex. In addition, unlike the other breeds, the boars of the Landrace breed showed an exponential type of relationship between body weight and backfat thickness. As they grow to become 100 kg or heavier, abrupt change in back fat thickness was confirmed. If the growth of body weight and backfat thickness is understood and the genetic relationship is taken advantage of like this, it would be possible to set desired body weight and backfat thickness, and thus help effectively set the shipping time. If not only the phenotype, but also genetic parameters about growth characteristics are estimated and analyzed additionally, more effective data can be generated.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.48 no.3
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• pp.377-385
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• 2015

The age and growth of the skipjack tuna Katsuwonus pelamis were determined using otoliths sampled from a Korean tuna purse seine fishery in the Western and Central Pacific Ocean from January 2005 to September 2006. A total of 312 otoliths were used to estimate the ages of skipjack tuna, which ranged from 1 to 7 years. The relationships between otolith ring radius (R) and fork length (FL) for female, male, and sex combined were FL = 19.74R + 1.50 ($r^2=0.54$), FL = 17.66R + 6.35 ($r^2=0.47$), and FL = 18.83R + 3.36 ($r^2=0.53$), respectively. The back-calculated fork lengths of each age ($FL_{year}$) were $FL_1=36.2cm$, $FL_2=43.3cm$, $FL_3=48.3cm$, $FL_4=52.6cm$, $FL_5=56.5cm$, $FL_6=60.8cm$, and $FL_7=63.2cm$. The relationships between fork length (FL) and total weight (TW) for female, male, and sex combined were $TW=0.00001FL^{3.19}(r^2=0.95)$, $TW=0.00001FL^{3.17}(r^2=0.95)$, and $TW=0.000009FL^{3.23}(r^2=0.95)$, respectively. The von Bertalanffy growth parameters of skipjack tuna estimated in this study were $L_{\infty}=77.4cm$, K = 0.176/year, and $t_0=-2.569years$.

• The Korean Journal of Malacology
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• v.27 no.1
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• pp.43-53
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• 2011

The gametogenic cycle and the spawning season in female and male Cyclina sinensis were investigated by quantitative statistical analysis using an image analyzer system, and the biological minimum size (the size at 50% of sexual maturity) was calculated by combination of quantitative data by size and von Bertalanffy's equation. Compared the gametogenic cycle by quantitative statistical analysis with the previous qualitative results in female and male C. sinensis, monthly changes in female and male gametogenic cycles calculated by quantitative statistical analysis showed similar patterns to the gonadal stages in female and male reproductive cycles by qualitative histological analysis. Comparisons of monthly changes in the portions (%) of each area to eight kinds of areas by quantitative statistical analysis in the gonads in female and male C. sinensis are as follows. Monthly changes in the portions (%) of the ovary areas to total tissue areas in females and also monthly changes in the portions of the testis areas to total tissue areas in males increased in March and reached the maximum in May, and then showed a rapid decrease from June to October. Monthly changes in the portions (%) of oocyte areas to ovarian tissue areas in females and also monthly changes in the portions of the areas of the spermatogenic stages to testis areas in males began to increase in March and reached the maximum in June in females and males, and then rapidly dropped from July to October in females and males when spawnig occurred. From these data, it is apparent that the number of spawning seasons in female and male C. sinensis occurred once per year, from July to October. Monthly changes in the number of the oocytes per mm2 and in the mean diameter of the oocyte in captured image which were calculated for each female slide showed a maximum in May and reached the minimum from December to February. Therefore, C. sinensis in both sexes showed a unimodal gametogenic cycle during the year. The percentage of sexual maturity of female and male clams ranging from 25.1 to 30.0 mm in length was over 50% and 100% for clams over 40.1 mm length. In this study, the biological minimum size (sexually mature shell lengths at 50% of sexual maturity) in females and males were 26.85 and 26.28 mm, respectively.

• 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.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.13 no.4
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• pp.179-183
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• 1980

The efficiency of energy transfer by a population of the farmed pacific oyster, Crassostrea gigas was studied during culture period of 10 months July 1979-April 1980, in Geoje-Hansan Bay near Chungmu City. Energy use by the farmed oyster population was calculated from estimates of half-a-month unit age specific natural mortality rate and data on growth, gonad output, shell organic matter production and respiration. Total mortality during the culture period was estimated approximate $36\%$ from data on survivor individual number per cluster. Growth may be dual consisted of a curved line during the first half culture period (July-November) and a linear line in the later half period (December-April). The first half growth was approximated by the von Bertalanffy growth model; shell height, $SH=6.33\;(1-e^{0.2421(t+0.54)})$, where t is age in half-a-month unit. In the later half growth period shell height was related to t by SH=4.44+0.14t. Dry meat weight (DW) was related to shell height by log $DW=-2.2907+2.589{\cdot}log\;SH,\;(2, and/or log $DW=-5.8153+7.208{\cdot}log\;SH,\;(5. Size specific gonad output (G) as calculated by condition index of before and after the spawning season, was related to shell height by $G=0.0145+(3.95\times10^{-3}{\times}SH^{2.9861})$. Shell organic matter production (SO) was related to shell height by log $SO=-3.1884+2.527{\cdot}1og\;SH$. Size and temperature specific respiration rate (R) as determined in biotron system with controlled temperature, was related to dry meat weight and temperature (T) by log $R=(0.386T-0.5381)+(0.6409-0.0083T){\cdot}log\;DW$. The energy used in metabolism was calculated from size, temperature specific respiration and data on body composition. The calorie contents of oyster meat were estimated by bomb calorimetry based on nitrogen correction. The assimilation efficiency of the oyster estimated directly by a insoluble crude silicate method gave $55.5\%$. From the information presently available by other workers, the assimilation efficiency ranges between $40\%\;and\;70\%$. Twenty seven point four percent of the filtered food material expressed by energy value for oyster population was estimated to have been rejected as pseudofaeces : $17.2\%$ was passed as faeces; $35.04\%$ was respired and lost as heat; $0.38\%$ was bounded up in shell organics; $2.74\%$ was released as gonad output, $2.06\%$ was fell as meat reducing by mortality. The remaining $15.28\%$ was used as meat production. The net efficiency of energy transfer from assimilation to meat production (yield/assimilation) of a farm population of the oyster was estimated to be $28\%$ during culture period July 1979-April 1980. The gross efficiency of energy transfer from ingestion to meat production (yield/food filtered) is probably between $11\%\;and\;20\%$.