• Korean Journal of Child Studies
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• v.1
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• pp.15-27
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• 1980

PURPOSE This study was intended to analyze the play-form of normal preschool children as related to age, sex, educational experience and social maturity. METHOD 1. Subjects The subjects of this study were eighty seven 3-, 4- and 5-year-old preschool children attending educational institutions in Seoul. 2. Instruments The instruments used in this study consisted of twenty one-minute observations in 5 preschool settings and a questionnaire designed to measure the children's social maturity filled in by their parents. The observations provided information on the children's free play, that is 1) play-form: solitary, parallel and group play 2) use/non-use of toys 3) behavior: play, activity, doing nothing, onlooking 4) stationary/moving dimensions 5) play group size The questionnaire measured such factors as communication, socialization, locomotion, self-help and self-direction. 3. Data Analysis Data analysis consisted of percentage and Chi square. RESULTS 1. Play-Form The relationship between age and play-form proved to be significant at the .05 level. That is, in both boys and girls, solitary play decreased with age and group play increased with age while parallel play maintained a similar position. The relationship between sex and play-form proved to be significant at the .05 level in 3-& 4-year-old children, but not significant in 5-year-old children. That is, in their $3^{rd}$ year boys engage in the solitary play more than girls and in their $4^{th}$ year boys engage in more group play than girls. 2. Toys Without differentiation of sex and age, cases of using toys in play exceed those cases where toys were not used. 3. Behavior The relationship between age and behavior proved to be significant at the .05 level in both boys and girls. That is, with increase of age, play decreased and activity increased in boys while play increased and doing nothing decreased in girls. 4. Moving Status Totally, moving occurred more frequently in play than stationary status. Moving proved not to have a significant relationship with age, but it did Navel a significant relationship with sex at the .05 level. That is, moving tended to increase with the increase in age in both boys and girls, but not at a significant level. Boys moved significantly more than girls in all three age levels. 5. The Relationship between Educational Experience and Play-Form There was a tendency for children with longer preschool experience to engage in less solitary play and more group play than children who had less than one semester of preschool experience, but this difference was not statistically significant. 6. The Relationship between Social Maturity and Play-Form The high social maturity group engaged in less solitary play and more group play than the low social maturity group, but this was not a statistically significant difference. 7. Play Group Size Play group size was 2~10 children, but the majority of play groups consisted of 2~3 children. There was a tendency for play groups composed of 2 children to decrease with age and play groups composed of 3 children to increase with age. No significant difference was found between the sexes in play group size.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.36 no.6
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• pp.646-653
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• 2003

Investigations were made on the population structure, sex ratio, growth, and recruitment patterns of Leptochela sydniensis in the southwestern coastal areas of Korea, between May 2000 and December 2001. Spawning period, fecundity, brood loss, reproductive output, and size at sexual maturity also were examined. The results of the sex ratio showed that females were more numerous than males during the overall study period. Parameters of growth were estimated using the modified von Bertalanffy growth function (VBGF) model incorporating seasonal variation into growth. Females grew somewhat faster and reached a larger size than males $(L\infty=12.80\;mm\;CL\;and\;K=0.70\;yr^{-1}\;or\;females,\and\;L\infty=12.08\;mm\;CL\;and\;K=0.69\;yr^{-1}$ for males). The structure of recruitment patterns obtained by the FiSAT program indicated one normally distributed group. Based on the occurrence of ovigerous females and the gonadosomatic index (GSI), the main spawning season was from June to August. Analysis of covariance indicated that brood loss was not observed during the incubation period. The size at which $50\%$ of females are mature is estimated as 5.48 mm CL.

• Journal of Aquaculture
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• v.22 no.1
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• pp.92-99
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• 2009

Population dynamics and sexual maturity of Neomysis japonica (Ishikawa and Oshima, 1951) were investigated from a shrimp farm in Tae-an, Korea. N. japonica was collected monthly at the shrimp farm belonging to the Marine and Fisheries Research Institute, the Soonchunhyang University from October 2002 to September 2003. The proportion of female was higher than that of male. The mean carapace length of male (2.42 mm) was larger than that of female (2.31 mm). Brood size increased with increasing female body size. The size of N. japonica at 50% sexual maturity was approximately 4.4 mm. N. japonica females grew faster and reached larger size than males. The mortality rate (z) calculated by length-converted catch curves was $3.46\;yr^{-1}$. The annual recruitment pattern of N. japonica had two major peaks. Log-transformed total length was significantly related with log-transformed carapace length.

• 한국해양학회지
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• v.18 no.2
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• pp.161-168
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• 1983

Age composition and reproductive period o the shad, Konosirus punctatus, in Cheonsu Bay were determined though analysis of sizi, ane and maturity of fish. Sampses were collected with trap in the bay mouth from May, 1981 to December, 1982. Shads start entering the bay for feeding and spawning in spring when water temperature exceeds 8$^{\circ}C$. They stay in inner part of the bay in summer nad move out to sea in autumn before water trmperature decreasea to 8$^{\circ}C$. Fish grows very rapidly during first summer after birth. Mean lengthes of 1-4 year old fishes were 12.2cm, 15.8cm, 17.6cm and 20.9cm, respectively. The largest and oldrst fish pbserved was 22.0cm long with age 4. Shads of Cheonsu Bay reach maturity at 2 years old at the size greater then 14cm. Data on size and age at first maturityindicate thzt maturity of shad depends on size and not on age. Spawning occurs from late April to late May when water temperature is between 8$^{\circ}C$ and 15$^{\circ}C$.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.53 no.1
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• pp.67-73
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• 2020

The maturity and spawning of the yellow goosefish Lophius litulon were studied using samples collected monthly from January to December 2018 from the coastal waters of Korea. We analyzed monthly changes in maturity stage, gonadosomatic index (GSI), total length (TL) at 50%, 75%, and 97.5% group maturity, egg diameter and fecundity. The spawning period was from January to June. The size of eggs spawned was between 0.30 to 1.28 mm. Fecundity varied between 328,314 to 1,624,783 eggs. The percentage of sexually mature females estimated from a logistic function was over 50% at 48.67 cm TL, 75% at 56.76 cm TL and 97.5% at 74.89 cm TL.

• Korean journal of applied entomology
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• v.57 no.4
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• pp.329-337
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• 2018

To increase the mating rate of Bombus ignitus used as insect pollinator, we investigated the sexual maturity time of B. ignitus. In investigating ovary development such as the number of eggs per ovariole and spermatheca size, the time of sexual maturity of queen was 10 days after eclosion. In case of male, the number of sperm was 246 thousand at immediately after eclosion, and was highest as 480 thousand at 9 days, and tended to show a dramatic decline at 35 days (87 thousand). The more mating time, the less the number of sperm. In consideration of number of sperms, the time of sexual maturity of male was 3-15 days after eclosion. In the sexual maturity time of queen in mating, the queen was not mated at immediately after eclosion, and showed a decrease in 20 days. In terms of the rate of mating and oviposition, the favorable time for mating of queen was 9-20 days. On the other hand, the male showed 3.3% of mating at immediately after ecolosion, showed the highest of 43.3% at 6 days after eclosion, and tended to decrease in 25 days. The sexual maturity time for mating of male was 6-20 days. In summary, our results indicate that sexual maturity time of B. ignitus in reproductive organs and mating is most favorable in 9-12 days after eclosion for queen and 6-9 days for male.

• Korean Journal of Veterinary Research
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• v.33 no.2
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• pp.277-283
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• 1993

In the present study, observations were made on the life-history of Lymnaea viridis under laboratory conditions, involving incubation period of the eggs and their hatching rate, shell length of the newly hatched snails, sexual maturity, size of the snails when the snail produced the first egg-mass, the number of eggs in each egg-mass, egg-laying, ovipostion, growth rate of the snails, and longevity of the snail. At temperatures between $19.8^{\circ}C$ to $22.5^{\circ}C$, incubation period of the eggs occupied 10~12 days, and after beginning of hatching, all young snails emerged completely from the egg-mass within 5 days. The hatching rate was 88%. The average shell length of the newly hatched snails was about 0.064cm. The rate of growth was extraordinarily rapid under good laboratory conditions. When two snails were reared in one culture vessel($20{\times}15{\times}5cm$) with blue-green algae at about $22^{\circ}C$, snail growth was optimal, taking 37 days to reach 1.2cm in shell length. Sexual maturity reached in about 19 days. The size of the snails at sexual maturity was $0.78{\pm}0.05cm$ in length and $0.47{\pm}0.04cm$ in width. The first egg-masses produced were $0.59{\pm}0.22cm$ in length and $0.34{\pm}0.08cm$ in width, and contained 7~38 eggs. The eggs are usually laid in water. The egg-laying was affected by food and temperature. Snails fed with blue-green algae at about $22^{\circ}C$ produced larger egg-masses than the snails fed with fish food at about $26^{\circ}C$. Under conditions of continuous activity and growth, the maximum expectation of life appears to be 109~350(mean 230) days. And the shell length of snails at death were 1.39~1.64cm.

• Animal cells and systems
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• v.4 no.4
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• pp.329-336
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• 2000

Life table experiments were performed in order to examine the effects of food quality on Moina macrocopa fed with four kinds of algal foods, Botryococcus sp., Scenedesmus subspicatus, Selenastrum capricornutum, and Chlorella sp., at $20^{\circ}C$ . The temperature effects on M. macrocopa were also assessed, feeding Chlorella at $17^{\circ}C$,$20^{\circ}C$,$25^{\circ}C$, and a combination of $28^{\circ}C$ (light) and $25^{\circ}C$ (dark). The cartilaginous Botryococcs cells were Inappropriate food for Moina. Among the foods tested, Chlorella was the food of the best quality in all accounts of life history traits. Moina grown on Chlorella showed higher net reproductive rate ($R_0$), longer mean and maximum longevities, earlier mean age at maturity, longer mean carapace length at maturity, larger mean clutch size, and shorter mean time interval between clutch productions than those grown on Selenastrum and Scenedesmus. An optimal temperature for Moina was $20^{\circ}C$ . When Moina were grown on Chlorella at $20^{\circ}C$, they showed the highest r, the highest $R_0$, the shortest T, the longest mean longevity, the earliest mean age at maturity, the longest mean carapace length at maturity, and the largest mean clutch size. The results of life table experiments showed that the individual and population growth patterns were much more affected by low temperature $17^{\circ}C$, than by high temperature ($\geq 20^{\circ}C$). In the optimal condition, the r value was very high, 5.1 in $d^{-1}$. In conclusion, the food quality and the temperature are the most important factors to govern the size and continuity of Moina population, by which the individual growth rates and reproductivity of members in the population can be controlled to survive in their environment such as small and temporary water bodies in nature.

• Animal cells and systems
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• v.13 no.1
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• pp.83-89
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• 2009

Investigations were made on population biology of Pampus echinogaster (Basilewsky, 1855) in the coastal areas of Korea, Yellow Sea, between August 2005 and July 2006. Population structure was not significantly different between male and females. Monthly variation of gonadosomatic index (GSI) of both sexes defined spawning period extending from March through July. A similar pattern was also observed in change at maturity stages. For males and females GSI was positively correlated with hepatosomatic index (HSI). Fecundity, ranging from 41,250 to 103,610 eggs, was related to body size, indicating that body size is the useful determinant of fecundity. The sexual maturity ($L_{50}$) was estimated as 14.98 cm TL for males and 19.32 cm TL for females. Parameters of growth estimated by the modified von Bertalanffy growth function model showed that the values of $L_{\infty}$ and K for combined data were 39.12 cm TL and 0.65 $yr^{-1}$. The growth performance index of this study (2.75) was higher than that of the previous study (2.45). This difference could be attributed to sampling method. The recruitment patterns indicated one normally distributed group. Percentage of the recruitment was 51.04% in the spawning season and the highest in August (19.78%).

• Korean Journal of Fisheries and Aquatic Sciences
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• v.38 no.4
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• pp.232-238
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• 2005

This paper describes reproduction, population structure, growth and size at sexual maturity of a deep-water mud shrimp (Solenocera melantho) in the adjacent waters of Geomun Island, Korea. The shrimp was caught by a beam trawl from November 1998 to December 1999. Spawning period was estimated by gonadosomatic index to be from August to early November with a peak in October to early November. Female shrimps were $12\%$ matured at 16 mm in carapace length, $33\%$ matured at 18 mm and $75\%$ matured at 22 mm. The size at $50\%$ maturity for female was estimated to be 20.65 mm in carapace length. Breeding season was estimated to be from August to early November with a peak in October to early November. The size at $50\%$ inseminated was 19.81 mm CL. The fecundity was 87,500-405,200 and related exponentially to carapace length and total weight. This species survived between 25 and 26 months. The maximum carapace length of females and males were 48 mm and 34 mm respectively. Sex ratio was $51.3\%$, and the females were preponderant. Growth was estimated by modified von Bertalanffy growth function incorporating seasonal variation in growth in both years females (K=1.019/yr and $L_{\infty}$=51.731 mm CL) grew faster, reaching a larger size at a given age than males (K=1.848/yr, and $L_{\infty}$=27.499 mm CL). This is indicated by differences in growth performance indices $(\varphi')$ between females (3.291) and males (3.145).