• Korean Journal of Fisheries and Aquatic Sciences
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• v.23 no.5
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• pp.385-393
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• 1990

Age and growth in length of anchovy juveniles were analysed from the samples collected from the coastal waters of Chonnam, Korea, in 1988 and 1989. Ages in days were determined by counting growth increments in otolith from 248 individuals. Growth in length versus age in days was well represented by Gompertz curve: $$L =5.76{\times}E xp(1.66 \times(1- E xp(-0.44\;t)))$$, or $$L=3.7{\times}E xp(1.99\times(1-E xp(-0.0614\;t)))$$. The mean growth rate was 0.38 mm/day from 20 days to 40 days. Growth rate was maximum at 10 days, and then decreased gradually. The growth of anchovy juvenile were nearly constant inspite of the sampling dates or stations.

• The Journal of Pediatrics of Korean Medicine
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• v.31 no.4
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• pp.31-38
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• 2017

Objectives The purpose of this study was to find out the clinically reliable relationships between the Risser sign and chronological age, bone age, menarche, and adult height prediction (AHP) and to evidence the reliability of the Risser sign. Methods This study had been carried out with 50 children who had their growth checked in an oriental medical hospital from January 2015 to February 2017. We investigated Risser sign in AP X-rays with iliac crest, bone age, AHP for all 50 children and the timing of menarche from the 22 girls in the study subjects. We also investigated a correlation between the Risser stage and the other indicators to analyze statistical data. Results The mean chronological ages of Risser 1, 2, 3 and 4 were 11.2, 12.6, 14.4, and 15.5 years respectively for the boys and 10.8, 12.2, 13.8 and 14.8 years respectively for the girls. The mean bone ages of Risser 1, 2, 3 and 4 were 12.3, 13.6, 15.7 and 16.5 years respectively for the boys and 11.7, 13.8, 14.3 and 14.9 years respectively for the girls. We analyzed 22 girls' Risser stages in accordance with the duration from menarche. The result showed that in the first six months after menarche, all girls were in Risser 1 and 2; in the next six months, the girls were in Risser 2 on average; in the next 12 months, all girls were in Risser 3 and 4; after more than two years from menarche, all girls were in Risser 4. The mean remaining growth height of Risser 1, 2, 3 and 4 were 27.8, 17.3, 4.4 and 1.0 cm respectively for the boys and 14.5, 5.1, 3.1 and 1.1 cm respectively for the girls. The Risser stage was correlated strongly with chronological age (Spearman's rho=0.707 (boy), 0.841 (girl)), bone age (Spearman's rho=0.869 (boy), 0.875 (girl)), duration from menarche (Spearman's rho=0.909) and remaining growth height (Spearman's rho=-0.784 (boy), -0.878 (girl)). Conclusions This study showed that the Risser sign can be useful in assessing skeletal maturity and predicting remaining growth height based on the Risser stage and the other growth indicators.

• Asian-Australasian Journal of Animal Sciences
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• v.22 no.7
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• pp.931-936
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• 2009

Body weights of 862 Angora goats between birth and 36 months of age, recorded on a semiyearly basis from 1988 to 2000, were used to estimate genetic, permanent environmental and phenotypic covariance functions. These functions were estimated by fitting a random regression model with 6th order polynomial for direct additive genetic and animal permanent environmental effects and 4th and 5th order polynomial for maternal genetic and permanent environmental effects, respectively. A phenotypic covariance function was estimated by modelling overall animal and maternal effects. The results showed that the most variable coefficient was the intercept for both direct and maternal additive genetic effects. The direct additive genetic (co)variances increased with age and reached a maximum at about 30 months, whereas the maternal additive genetic (co)variances increased rapidly from birth and reached a maximum at weaning, and then decreased with age. Animal permanent environmental (co)variances increased with age from birth to 30 months with lower rate before 12 months and higher rate between 12 and 30 months. Maternal permanent environmental (co)variances changed little before 6 months but then increased slowly and reached a maximum at about 30 months. These results suggested that the contribution of maternal additive genetic and permanent environmental effects to growth variation differed from those of direct additive genetic and animal permanent environmental effects not only in expression time, but also in action magnitude. The phenotypic (co)variance estimates increased with age from birth to 36 months of age.

• Asian-Australasian Journal of Animal Sciences
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• v.5 no.4
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• pp.659-664
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• 1992

Twelve day old Pabna zebu calves of similar weights were assigned at random to 3 different calf starter-rations namely $T_0$, $T_1$ and $T_2$ to determine the effect of feeding regimes and growth pattern of calves upto 3 months of age. Calves allowed to intake starter 0.5 percent of body weight from 2nd week on to 7th weeks of age, while starter at 1 percent of body weight was allowed later on upto 13th weeks of age. Calves started to intake green grass after 2nd to 3rd weeks and average intake per day was limited to 1 kg upto the end of experiment, while calves started to take rice straw ad libitum after 6th weeks of age. Colostrum feeding was offered ad libitum and in addition calves suckled their dam's milk shortly before and after milking usually in the morning and evening. Growth of calves in different treatment groups was found statistically insignificant. The mean growth rate per head per day ranged from 196.43-375.0 g for $T_0$ group, 185.72-360.72 g for $T_1$ group and 180.1-385.72 g for $T_2$ group respectively between 1st to 7th weeks of age while the growth rate ranged from 309.53-328.57 g for $T_0$, 304.29-342.86 g for $T_1$ and 304.77-333.30 g for $T_2$ groups respectively from 9th weeks on to the end of the experiment.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.45 no.3
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• pp.246-252
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• 2012

The age and growth of the blackthroat seaperch Doederleinia berycoides was investigated based on samples captured in the southern seas of Korea from January to December, 2006. Age was estimated by analyzing otolith growth rings. The spawning period was extrapolated from August to November based on monthly changes in the gonad somatic index. The relationship between total length and otolith radius was analyzed separately for each sex with TL=-15.6174+10.3274R for females and TL=-4.4083+7.0749R for males. From the parameters calculated using average total length and weight when the year ring was formed, the growth of D. berycoides was expressed by von Bertalanffy growth equations as $L_t=34.71(1-e^{-0.2557(t+0.2078)})$, $W_t=713.85(1-e^{-0.2557(t+0.2078)})^{3.1972}$ for females, $L_t=27.37(1-e^{-0.3388(t+0.7362)})$, $W_t=353.91(1-e^{-0.3388(t+0.7362)})^{3.1647}$ for males, and $L_t=34.20(1-e^{-0.2530(t+0.2871)})$, $W_t=674.10(1-e^{-0.2530(t+0.2871)})^{3.1171}$ for pooled sexes, where L is total length at age t.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.22 no.5
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• pp.332-341
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• 1989

Stomach contents and microstructures in otolith of Chaenogobius laevis were analyzed for the determination of age, growth and food. By comparaing structural similarity in a series of growth increments from three samples collected in a two-week interval, daily deposition of growth increments in otolith can be validated. Growth in length as daily basis was well represented by Gompertz curve: $L= 5.73{\cdot}\;e^{15.06}(1-e^{-0.0015t})$ for the fish age of $46\~102$ days. Mean growth rate increased from 0.40 mm/day for the age of $50\~60$ days to 0.85 mm/day for the age of $80\~100$ days. Chasnobius laevis showed a carnivorous feeding behavior and its major food items were polychaetes, amphipods and copepods. Small individuals ($15\~30$ mm SL) preyed heavily on copepods as well as polychaetes. However, the portion of copepods in stomach contents was decreased with increasing fish siEe, and this decrease was compensated by an increased consumption of amphipods.

• Ocean and Polar Research
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• v.28 no.3
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• pp.237-243
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• 2006

The ages of sandfish, Arctoscopus japoninis sampled from the eastern sea of Korea, were determined by the transverse section method of otoliths. Ages were assigned to every individual according to the number of opaque zones, and then fitted to the von Bertalanffy growth equation. Estimated equations were $L_t=25.90(1-e^{-0.2976(t+0.4447)})$ for females and $L_t=21.38(1-e^{-0.2917(t+1.2087)})$ for males, where t is age (year) and $L_t$, is body length (mm) at age t. These two equations were significantly different and the body length of females calculated from the equation was larger than that of males except at 1 year old.

• The korean journal of orthodontics
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• v.24 no.4 s.47
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• pp.851-860
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• 1994

Before 1970, mandibular overgrowth was known as main cause of skeletal Class III malocclusion in growing children ; however, recent study reports that many skeletal Class III malocclusion patients also show maxillary deficiency. Since 1972, when Delaire re-accommodated Protraction Head Gear (P.H.G.), many researchers have reported that skeletal Class III discrepancies could be corrected through use of P.H.G., which induces anterior movement of maxilla and change in mandibular growth pattern into infero-posterior direction ; nevertheless, it is very difficult to predict resultant changes of orofacial region. The purpose of this study was to find out what treatment effect P.H.G. has on different study samples. Author divided 51 skeletal Class III malocclusion patients with maxillary deficiency who were treated with P.H.G. into different study groups depending on sex, treatment beginning age, intraoral appliance, and facial growth pattern. By doing so, following results were obtained. 1. Treatment beginning age and Sex Four age groups (5.8 to 8 year-old, 8 to 10 year-old, 10 to 12 year-old, 12 to 14 year-old) were compared, and no significant difference was observed. (p<0.05) There was no significant difference between the sex groups, either. (p<0.05). 2. Intraoral appliance Treatment effects of study groups that used R.P.E.(mean age of 10.2) and Labio-Lingual appliance(mean age of 8.9) were compared. There was no significant difference depending on the type of intraoral appliance that was used. (p<0.05) 3. Facial growth pattern 1) Amounts of SNB and ANB corrections were smaller in clockwise growth pattern group than those in normal or counterclockwise growth pattern group. (p<0.05) 2) Amounts of increase in Wits appraisal and mandibular plane angle were greater in counterclockwise growth pattern group than those in normal or clockwise growth pattern group. (p<0.05) 3)Amounts of increase in articular angle were greater in counter lockwise growth pattern group than those in clockwise growth pattern group. (p<0.05)

• Journal of the Korean Dietetic Association
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• v.9 no.2
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• pp.106-113
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• 2003

The purpose of this study was to compare the growth development between age-matched 51 postmenarcheal girls (mean age 153.1$\pm$5.8 month) who were rapidly maturing and 51 premenarcheal girls (mean age 153.1$\pm$5.7 month) who were slowly maturing. Anthropometirc measurements were taken for height, body weight, body fat(%), waist and hip circumferences of subjects. These measurements of menarcheal girls were significantly higher than those of nonmenarcheal girls. There was no significant difference in BMI distribution between two groups. However, 43.2% and 20.0% respectively in the menarcheal and nonmenarcheal girls had body fat levels of 30% or above. There were significant differences in the anthropometric measurements during past 4 years from 3rd grade elementary school to present. The greatest difference between the two groups were the amount and the rate of increased height and body weight from age 9 to 10. Among menarcheal girls, height, body weight, BMI, and Röhrer index were positively related to the onset of menarche. Distinctively, there was a stronger relationship between age at menarche and anthropometric measurements when the girls were 5th grade elementary school children. These findings support that during childhood and puberty, obese girls grow faster and have earlier menarche. Furthermore, the importance of prevention of obesity was recognized in order to accelerate growth of height among the girls by delaying the age of menarche.

• Asian-Australasian Journal of Animal Sciences
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• v.22 no.7
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• pp.937-942
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• 2009

The aim of this study was to analyze the effects on growth and muscle development during the growing period of the sex-linked dwarf gene in the background of a Taiwan Country chicken strain, L2, selected for egg production. Eight crossbred males, heterozygous for the DW*DW mutation, were each backcrossed to six females of the L2 strain to produce two genotypes of BC females, either normal (DW*N+/-) or dwarf (DW*DW/-). The experiment included 251 normal and 207 dwarf pullets. The effect of the dwarf gene on body weight and shank length was highly significant from 2 weeks of age. The reduction of body weight by the dwarf gene reached 34.8% and 37.4% as compared to normal sibs at 16 and 20 weeks of age, respectively. Parameters of the growth curve were estimated: the age at inflection (TI) was higher in normal pullets (66.9 days) than in dwarf pullets (61.2 days). A significant effect of the dwarf gene on single muscle fiber cross-section area was found from 12 weeks of age onwards, whereas the dwarf gene had no effect on the total number of muscle fibers. Comparing the effect of the dwarf gene on shank length at different ages revealed an earlier effect on skeleton growth, observed from 2 weeks of age, than on muscle development, which was affected from 8 to 12 weeks of age.