• Korean Journal of Fisheries and Aquatic Sciences
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• v.42 no.6
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• pp.600-603
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• 2009

Genetic and phenotypic parameter estimates for measurement traits were obtained from pacific oyster Crassostrea gigas at nine months old. For the growth-related traits among nine months old pacific oyster, heritabilities of shell length, shell height, shell width, total weight, body weight and shell weight were estimated as 0.4855, 0.5248, 0.0884, 0.7236, 0.7726 and 0.6957, respectively. Genetic correlations among the growth-related traits of pacific oyster at nines month old, shell length, shell height, shell width, total weight, body weight, shell weight were showing highly positive correlations. Breeding value on growth-related traits of pacific oyster at nine months old were estimated as shell length -7.044-11.870, shell height -11.380-18.370, shell width -1.234-2.831, total weight -8.339-17.140, body weight -1.813-3.507 and shell weight -4.422-8.837. The results show that there is quite substantial additive genetic variance for measurement traits in pacific oyster that can be exploited through selective breeding.

• Journal of Ecology and Environment
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• v.30 no.2
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• pp.109-119
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• 2007

The effect of water flow on the growth of Gafrarium tumidum was studied in the field using open cages constructed with stainless steel net and perspex in which holes were drilled. Cages with different flows (25, 50 and 75% of the control) were made by varying the area of perspex being drilled. Reduction in flow rate was directly proportional to the undrilled area, and the mean flow rate of the different treatment groups varied from 3.12 cm/s for the 25% exposure to 12.48 cm/s for the control cages. At the end of the 3-month experiment, no significant differences in sediment characteristics were found among the treatments. Growth in shell length, shell weight and tissue dry weight was, however, positively correlated with flow rate. Percentage increases ranged from $3.0{\sim}8.3%$ for shell length, $9.9{\sim}23.1%$ for shell weight and $17.2{\sim}53.3%$ for tissue dry weight. Condition index of the clam was not significantly different among the treatments. Seston depletion effect could reduce growth in G. tumidum only when water flow was reduced to 25% of the control. G. tumidum also exhibited different responses in shell and tissue growth at low flow rates, in which shell growth continued to decrease as flow rate decreased whereas tissue growth was relatively independent of low flows at 25 and 50% of the control. It was suggested that when seston flux was reduced at slow flows, it would be a better strategy for G. tumidum to channel energy for gonad development instead of shell growth during the reproductive stage.

• The Korean Journal of Malacology
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• v.21 no.1
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• pp.57-64
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• 2005

Samples of Corbicula japonica Prime of Jujin estuary in Gochang were collected from July 2000 to September 2001. Age of C. japonica was determined from the rings on the shell. The relationship between shell length and ring radius in each ring group was expressed as a regression line. Therefore, there is a correspondence in each ring formation. Based on the monthly variation of the marginal index (MI') of the shell, it is assumed that the ring of this species was formed once a year during the period of February and March. The relationship between shell length (SL; mm) and total weight (TW; g) was expressed by the following equation: TW = 1.0942 ${\times}10^{-4}SL^{3.3217}$ ($r^2$ = 0.9905). Shell length (SL) and shell height (SH; mm) was highly correlated with shell height as the following equation: SH = 0.9174 SL - 0.9935 ($r^2$ = 0.9885). The shell length (SL) - shell width (SW) relation was also expressed by the following equation; SW = 0.5925 SL - 1.1706 ($r^2$ = 0.9726). Growth curves for shell length and total weight fitted to the von Bertalanffy's growth curve were expressed as: $$SL_t = 46.4861[1-e^{-0.3383(t+0.0958)}]$$, $$TW_t = 34.54[1-e^{-0.3383(t+0.0958)}]^3.3217$$.

• The Korean Journal of Ecology
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• v.1 no.2
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• pp.49-56
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• 1977

For the culture the population growth, shell length and spawning seasons of Gomphina veneriformis, and its environmental factors, were investigated at the Jeju coastal regions. from Feburuary, 1975 to March, 1976. The soil movements of the tidal flats where the clams inhabited were relatively rapid during the strong tidal actions. The rate of population growth were rapid from April to September, then became obsure. The relative growth equations of the shell height (SH) and the shell breadth (SB) against the shell length (SL) of the clams were as follows: Changhung : SH=0.751 SL + 0.685, SB=0.448 SL-0.630 Pyoson : SH-0.775 SL - 0.115, SB=0.464 SL-1.008 Hwhason : SH=0.794 SL - 0.923, SB=0.485 SL-1.155 Kwhagzee : SH=0.771 SL - 0.644, SB=0.455 SL-1.049 The meat weight increases of the clams were continued from March to late June, then it decreased sharply up to late August. The spawning of the clams seems to be late from June to Spetember in the regions studied.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.35 no.6
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• pp.557-562
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• 2002

This study was to estimate population growth parameters of the freshwater bivalve, Corbicula (Corbiculina) papyacca (Heude) in Korea. Samples were collected from Jojong stream in Chungpyeong from September 1999 to August 2000. Ages were determined from the ring of shell, The shell length of the samples ranged from 4,2 mm to 28.1 mm, The ring on the surface of shell was formed once a year from January to March, Marginal increment analysis of shell rings indicated that annuli were formed in June. Spawning period was estimated to be May to August with a peak between June and July through fatness analysis, and thus rings were considered to be true annual marks. Von Bertalanffy's growth parameter were estimated from a nonlinear method with the value of logical maximum shell length ($L_{propto}$) was 34,36 mm, K was 0.1531/year, logical age of shell length 0 ($t_{0}$) was -0,5246 year, and logical maximum total weight ($W_{propto}$) was 11.42 g.

• The Korean Journal of Malacology
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• v.26 no.3
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• pp.227-234
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• 2010

A comparative analysis of size and age structures of coastal subfossil shell assemblages of the shortnecked clam Ruditapes philippinarum from open and protected bays of Cheju Island (Korea) was carried out. On the whole, taking into account the damage of small fragile shells, size and age structures of the shell assemblages corresponded to the classical curve of bivalve population distribution when its mortality diminishes with age increase up to a certain threshold. It was found that shell samples from open bays of the western, southern and eastern coasts included shells of smaller and younger individuals (L ${\leq}$ 40 mm, ${\leq}$ 4 years) than samples from the eastern protected bay (L ${\leq}$ 54.5 mm, ${\leq}$ 6 years). Evidently, strong wave activity was the reason for a short life-span of the clams from the open areas. Growth was investigated retrospectively by annual growth rings on the shells. Growth rates of the clams from the various coasts of Cheju Island differed. However, growth rates of the clams from different biotopes at the same (eastern) side of the Island were similar. Shell height/length and width/length ratios statistically significantly increased with the clam age increase. Most likely, the reason for such shell shape alteration is that more conglobated individuals more survive being more energy-optimal than oblong specimens.

• The Korean Journal of Malacology
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• v.29 no.2
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• pp.121-127
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• 2013

In this study, growth-line analysis was carried out on the hard clam (Meretrix petechialis) collected from the Neolithic shell middens in Daejuk-ri, Seosan, Korea, to reconstruct palaeoenvironment. Growth increments of 206 specimens of the clam were examined. The ages of the specimens were determined from the rings on the shells. The relationship between shell length and ring radius in each ring group was expressed as a regression line, indicating a correspondence in each ring formation. Growth pattern of the midden specimens was compared to that of modern ones collected from Gimje, Jeonbuk. Growth curves for shell length fitted to the von Berta anffy's growth curve were expressed respectively as follows: $SL_t=102.9025[1-e^{-0.18657(t+1.0906)}]$ in the shell midden specimens, $SL_t=104.2583[1-e^{-0.2277(t+0.7499)}]$ in the modern ones. The relationship between shell length (SL; mm) and shell height (SH; mm) was expressed by the following equations: SH = 0.7791 SL + 3.6636 ($R^2$ = 0.946) in the midden specimens, SH = 0.8103 SL + 0.5145 ($R^2$ = 0.991) in the modern ones. The results of the tests regarding the differences between regression coefficients and elevations of growth curves of these two populations demonstrate that the slopes were not significantly different (p < 0.05), but the elevations were (p > 0.05). However, overall growth curves of the midden and modern populations were not significantly different, indicating that shell growth environments of the two areas are similar. Therefore, it is likely that sea temperature near the midden area could be similar to that of present Gimje area, and thus temperature during the period of the midden formation could be higher than presently known.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.11 no.4
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• pp.116-121
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• 2006

Samples of Meretrix lusoria were collected monthly from the tidal flat of Simpo, Puan-gun, Chollabuk-do, west coast of Korea from April 2004 to March 2005. Age of M. lusoria was determined from the rings on the shell. The relationship between shell length and ring radius in each ring group was expressed as a regression line. Therefore, there is a correspondence in each ring formation. Based on the monthly variations in the marginal index (MI') of the shell, it is assumed that the ring of this species was formed once a year during the period of February to April. The relationship between shell length (SL) and shell height (SH; mm) was highly correlated with shell height as the following equation: SH = 0.8103 SL + 0.5145 $(r^2=0.991)$. The shell length (SL) - shell width (SW) relation was also expressed by the following equation: SW = 0.4897 SL + 0.0315 $(r^2=0.976)$. Shell length (SL; mm) and total weight (TW; g) was expressed by the following equation: $TW=2.9195\times10^{-4}\;SL^{2.9547}\;(R^2=0.991)$. Shell length (SL) and shell height (SH; mm) was highly correlated with shell height as the following equation: $SH=0.8103\;SL+0.5145\;(R^2=0.991)$ The shell length (SL) - shell width (SW) relation was also expressed by the following equation: $SW=0.4897\;SL+0.0315\;(R^2=0.976)$. Growth curves for shell length and total weight fitted to the von Bertalanffy's growth curve were expressed respectively as: $SL_t=104.9[l-e^{-0.2235(t+0.7677)}],\;TW_t=280.8[l-e^{-0.2235(t+0.7677)}]^{2.9547}$.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.11 no.4
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• pp.152-157
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• 2006

Samples of Meretrix lusoria were collected monthly from the tidal flat of Simpo, Puan-gun, Chollabuk-do, west coast of Korea from April 2004 to March 2005. Age of M. lusoria was determined from the rings on the shell. The relationship between shell length and ring radius in each ring group was expressed as a regression line. Therefore, there is a correspondence in each ring formation. Based on the monthly variations in the marginal index (MI') of the shell, it is assumed that the ring of this species was formed once a year during the period of February to April. The relationship between shell length (SL) and shell height (SH; mm) was highly correlated with shell height as the following equation: SH = 0.8103 SL + 0.5145 $(r^2=0.991)$. The shell length (SL) - shell width (SW) relation was also expressed by the following equation: SW = 0.4897 SL + 0.0315 $(r^2=0.976)$. Shell length (SL; mm) and total weight (TW; g) was expressed by the following equation: $TW=2.9195\times10^{-4}\;SL^{2.9547}\;(R^2=0.991)$. Shell length (SL) and shell height (SH; mm) was highly correlated with shell height as the following equation: $SH=0.8103\;SL+0.5145\;(R^2=0.991)$ The shell length (SL) - shell width (SW) relation was also expressed by the following equation: $SW=0.4897\;SL+0.0315\;(R^2=0.976)$. Growth curves for shell length and total weight fitted to the von Bertalanffy's growth curve were expressed respectively as: $SL_t=104.9[l-e^{-0.2235(t+0.7677)}],\;TW_t=280.8[l-e^{-0.2235(t+0.7677)}]^{2.9547}$.

• The Korean Journal of Malacology
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• v.23 no.2
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• pp.227-233
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• 2007

The amount of Batillus cornutus captured in Jeju Island was about 2,000 tons/year for three years after 2000. The mean size of B. cornutus by shell height was 7.7 cm in 2001, 7.9 cm in 2002, and 8.1 cm in 2003. Local mean size of B. cornutus by shell height was 8.7 cm in eastern waters, 7.4 cm in western waters, 7.8 cm in southern waters, and 7.7 cm in northern waters of Jeju Island. To investigate the effect of the growth pattern, an experiment was conducted: the samples were tagged and released in southern coastal waters of Jeju Island on 2nd April (a release test) and 29th October (a recapture test) in 2003. The release stations were two sites, natural reef and artificial reef, where their environmental conditions were different from each other. In April, the size of B. cornutus released in the natural reef was 6.2 cm in mean shell height, and 58.9 g in mean shell weight. The size of B. cornutus released in the artificial reef was 6.6 cm in mean shell height, and 65.9 g in mean shell weight. During the release period, most of B. cornutus were not moved much (less than 10 m) from the original release sites. When B. cornutus was recaptured in October after 7 months, the size of B. cornutus released in the natural reef became 7.4 cm in mean shell height, and 89.4 g in mean shell weight. The size of B. cornutus released in the artificial reef became 7.2 cm in mean shell height, and 84.9 g in mean shell weight. This indicates that the growth rate of B. cornutus released in the natural reef was higher than that of B. cornutus in the artificial reef. These differences in the growth of B. cornutus between study sites were ascribed to the abundance of marine algae grazed by immobile B. cornutus. Namely, with relatively high growth rate of B. cornutus in the natural reef, the number of species (23 species) and biomass (26,703.4 g) of algae were more diverse and abundant than those (7 species and 17,018.4 g) of algae in the artificial reef. The growth of B. cornutus in the natural reef was also correlated to high water temperature $(15.5-25.9^{\circ}C)$.