• Fisheries and Aquatic Sciences
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• v.24 no.1
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• pp.53-62
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• 2021

Gindai (Pristipomoides zonatus) is one of six snappers in a management complex called the Deep 7 of the Hawaiian Islands. Little is known about its life history and a preliminary analysis of otolith thin sections indicated the species may exhibit moderate growth with a lifespan approaching 40 years. Preliminary age estimates from the previous study were reinvestigated using the same otolith sections in an attempt to validate those ages with bomb radiocarbon (¹⁴C) dating. From the misalignment of birth years for the otolith ¹⁴C measurements with regional references - the post-peak bomb ¹⁴C decline period - it was concluded that previous ages were inflated from overcounting of the earliest growth zone structure in otolith sections. The oldest gindai was re-aged to 26 years once the age reading was adjusted for early overcounting, 13 years younger than the original estimate of 39 years for this fish. In general, the earliest otolith growth of gindai was massive and complicated by numerous subannual checks. The approach of lumping the early growth structures was supported by the alignment of ¹⁴C measurements from otolith core material (first year of growth). The result was greater consistency of calculated birthdates with the ¹⁴C decline reference, along with minor offsets that may indicate age estimation was imprecise by a few years for some individuals. The revised von Bertalanffy growth function applied to the validated age-at-length estimates revealed more rapid growth (k = 0.378 cf. 0.113) and a lifespan of approximately 30 years. The findings presented here are a case study of how the bomb ¹⁴C decline period can be used as a tool in the refinement of age reading protocols.

• Journal of the Korean Society of Fisheries and Ocean Technology
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• v.54 no.1
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• pp.54-64
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• 2018

The age and growth of Pleurogrammus azonus in the coastal of Gangwon-do, East Sea were determined, from monthly samples of commercial catches, caught by the gill net and set net fishery from January to December in 2008. Gonadosomatic index (GSI) began to increase in September, and reached the maximum between November and December. After spawning GSI began to decrease from January. The annuli of P. azonus are formed once a year, with the boundary between opaque and translucent zones forming from December to January. The relationships between fork length (FL) and body weight (BW) were $BW=0.005FL^{3.240}$($R^2=0.963$) for females and $BW=0.006FL^{3.238}$($R^2=0.946$) for males. The FLs at annuli formation in otoliths were back-calculated from the otolith-length relationship and were adjusted to von Bertalanffy growth curves to $FL_t=70.54(1-{\exp}^{(-0.099(t+1.188))})$ for females and $FL_t=51.87(1-{\exp}^{(-0.135(t+1.697))})$ for males. Until the age of 3 years, males grew faster than females; however, from the age of 4 years, females grew faster than males. In the future, we want to study the relationship between early growth and water temperature changes in the East Sea.

• Korean Journal of Ichthyology
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• v.24 no.2
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• pp.110-117
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• 2012

Hatching date and early growth of Pacific cod Gadus macrocephalus were estimated by examination of otolith microstructure of Pacific cod juveniles collected in Jinhae Bay of Korea from May to June, 2008. Water temperature during the main spawning time ranged from 7 to $9^{\circ}C$ according to the geographic distribution of temperature measured from November to May between 2006 and 2009. The spawners were collected from December to February between 2006 and 2008, and the gonadosomatic index of spawners was larger in females than in males, showing a peak in January. Total length of juveniles ranged from 37.5 to 94.9 mm ($63.2{\pm}11.0mm$; mean${\pm}$SD). The number of daily growth increments in juvenile otoliths were on average $102{\pm}15$ in May 17 samples, $119{\pm}16$ in May 29 ones and $116{\pm}18$ in June 3 ones. Hatching dates estimated from the number of daily growth increments ranged from late December to mid-March, showing the peak between late January and mid-February. Daily growth in total length (TL, mm) can be adjusted to the Gompertz curve: $TL_t=123.2{\exp}\{-{\exp}[-0.0165(t-81.8)]\}$ ($r^2$=0.93, n=273).

• 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.

• Korean Journal of Ichthyology
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• v.18 no.1
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• pp.45-54
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• 2006

Age and growth of the small yellow croaker, Larimichthys polyactis were estimated using right sagittal otoliths of 506 fish specimens from March to December, 2002 and from January to February, 2005 in the South Sea, part of the East China Sea of Korea. Examination of outer margins of the otolith showed that the opaque zone was formed once a year. Marginal increment of the otolith formed annual rings from May and June at the beginning of spawning season. In the relationship between total length and body weight, a multiplicative error structure was assumed because variability in growth increased as a function of the length, and the estimated equation was $BW=0.0044TL^{3.2502}$ ($R^2=0.97$). The relative growth as body weight at total length has significant difference between females and males (P<0.05). For describing growth of the small yellow croaker, Larimichthys polyactis a von Bertalanffy growth model was adopted. The von Bertalanffy growth curve had an additive error structure and the growth parameters estimated from non-linear regression were $L_{\infty}=33.88cm$, K=0.20/year and $t_0=-2.39year$. Growth at age of males and females shows no significant difference (P>0.05). Most examined fish were 1, 2 and 3 years old, although the oldest fish were 7 old for males and 8 for females.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.12 no.2
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• pp.112-120
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• 2007

This paper reviews the use of parasites as 'biological tags' for studying stock analysis of salmonid fishes. Numerous definitions of stock concepts exist, but most of them essentially define a group of fish as having similar biological characteristics and being self-reproducing as stocks. It is important to manage fish stocks for human consumption and sustainable production and especially for salmonid fishes. Because these fry are considered as each country's property, it is necessary to identify and discriminate each fish stock in the open sea. Methods of separating fish stocks are very diverse. Artificial tags, parasites, otoliths scales and genetic characters have been used for stock analysis and each method has advantages and disadvantages. Of these parasites can be good biological tags because they are applied by nature at no cost. Parasites can be infected with susceptible host fishes when they enter into certain areas. Then if they move to the outside and are caught researchers can infer that the fish had been in the endemic area for a period of time during their life. Hence the host fish can be considered as naturally 'tagged' by parasites. However, if they do not pass the parasites-endemic. area, they will harbour no parasites. Therefore, researchers can discriminate each fish stocks and trace their migration routes with these biological tags. In this paper, several examples on the use of parasites as biological tags for studying salmonids, as well as other species, are listed. The advantages and limitations of parasites as biological tags are also discussed. Chum salmon (Oncorhynchus keta), the main salmonid species migrating to Korea, is distributed all around the North Pacific. Korean chum salmon are generally thought to move to the Sea of Okhotsk, the western North Pacific and the Bering Sea. However, there is no clear information on the distribution and migration pathways of Korean chum salmon, and no markers exist for separating them from others yet. Recent Korean chum salmon stock analysis including parasites information are mentioned.