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Stock Identification of Chum Salmon (Oncorhynchus keta) Using Trace Elements in Otoliths PDF

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Journal of Oceanography, Vol. 61, pp. 305 to 312, 2005 Stock Identification of Chum Salmon (Oncorhynchus keta) Using Trace Elements in Otoliths DONGWHA SOHN1, SUKYUNG KANG2,3 and SUAM KIM1* 1Department of Marine Biology, Pukyong National University, Busan 608-737, Korea 2Department of Marine Science, Pusan National University, Busan 609-735, Korea 3National Fisheries Research and Development Institute, Busan 619-902, Korea (Received 31 January 2004; in revised form 11 June 2004; accepted 11 June 2004) The relationship between trace elements in chum salmon otoliths and in their rearing Keywords: water was investigated to develop ways to distinguish chum salmon stocks in Korea. ⋅⋅⋅⋅⋅Chum salmon, Rearing water and otoliths of hatchery-reared chum salmon fry were collected from ⋅⋅⋅⋅⋅otolith, three major hatcheries (Yangyang, Samchuk, and Uljin) on the east coast of Korea in ⋅⋅⋅⋅⋅trace element, ⋅⋅⋅⋅⋅chemical composi- spring 2001 and 2002. Trace elements in the otoliths and rearing water were analyzed tion, using inductively coupled plasma mass spectrometry (ICP-MS) at the Korea Basic ⋅⋅⋅⋅⋅stock identifica- Science Institute. The chemical composition of rearing water and otoliths of the salmon tion. fry at specific sites did not vary significantly through the study period. The ratios of some trace elements to Ca in rearing water, such as Sr/Ca and Ba/Ca, was clearly reflected in the chemical composition of otoliths, although the absolute concentra- tions were different. These two elements may be useful in distinguishing between salmon hatcheries, which have different chemical environments. Discriminant analy- sis with the ratios of eight elements to Ca (Na/Ca, Mg/Ca, Al/Ca, Cu/Ca, Sr/Ca, Ba/ Ca, Mn/Ca, and Zn/Ca) revealed a distinct separation of natal area in stocks. The analysis of otolith chemistry may be an effective technique for identifying the origins of wild salmon caught at sea. 1. Introduction The distribution and migration paths of salmon have There are seven species of salmon (chum, sockeye, not been clearly understood because little is known about pink, chinook, coho, masu, and steelhead) in the North the salmon’s life at sea. It is generally accepted that chum Pacific Ocean, all of which are anadromous and return to salmon released from the Asian continent distribute more their natal waters to spawn (Groot and Margolis, 1991). widely in the ocean than do those from North America. Japan began a salmon enhancement program in 1878, and Young salmon released from Korean streams reside in most Pacific Rim countries have maintained enhancement estuarine and coastal areas in the spring and might move programs throughout the 20th century. In Korea, an arti- to the Sea of Okhotsk along the North Korean, Russian, ficial propagation program for chum salmon began in and Japanese coasts during the spring and summer. As 1913 on the northeastern coast. There was not much arti- they mature, they move to the western North Pacific and ficial propagation of chum salmon in South Korea until the Bering Sea. After spending some years in the Bering the Yangyang hatchery opened in the mid-1980s (Seong, Sea or the North Pacific Ocean, they migrate to their na- 1999). Three major hatcheries (Yangyang, Samchuk and tal streams to spawn in the autumn when they are three to Uljin) currently carry out artificial fertilization activity five years old (Jung et al., 2003; Fig. 1). in the autumn and release chum salmon fry into 18 adja- Stocks or populations are fundamental units for man- cent streams on the east coast of the Korean Peninsula aging fisheries resources. Each stock, in which individu- during the early spring. About 220 million fry were re- als share the same habitat or distribution, is part of the leased from these hatcheries between 1985 and 2002. same gene pool through sexual reproduction of interbreed- ing individuals within the population. There are many methods of identifying stocks, including mark and recap- ture, analysis of catch data, and comparison of life his- * Corresponding author. E-mail: [email protected] tory characteristics, parasites, genetic analysis, morphol- Copyright © The Oceanographic Society of Japan. ogy and otolith microchemistry (Begg and Waldman, 305 emental fingerprints (Campana et al., 1995; Thorrold et al., 1997, 1998; Thresher, 1999; Patterson et al., 1999; Gillanders and Kingsford, 2000; Campana and Thorrold, 2001; Rooker et al., 2002) because they accumulate ele- ments from habitats throughout the fish’s life (i.e., the first part of the otolith to be formed would reflect the natal habitat and the most recently formed part of the oto- lith would reflect the most recent habitat of the fish). We examined the chemical composition of salmon otoliths and of rearing water from three hatcheries in South Korea (Yangyang, Samchuk, and Uljin). Based on Fig. 1. Three plausible migration pathways of released chum the relationship between the chemical compositions of salmon from Korea to the North Pacific Ocean (Jung et al., 2003). salmon otoliths and of rearing water, we tried to develop a way to distinguish salmon stocks, assuming that there was no alteration of otolith chemistry after formation. 2. Materials and Methods In the spring of 2001 and 2002, a total of 26 and 849 salmon fry respectively were collected from the three major hatcheries along the eastern coast of the Korean Peninsula (Fig. 2). Fry were brought to the laboratory, and fork length and body weight were measured (Table 1). The sagittal otoliths were extracted, rinsed in distilled water, cleaned for 10 min in an ultrasonicator, and dried. Because of their small size, 20–40 otoliths were composited for chemical analysis as one specimen in or- der to reduce variability and to obtain high enough con- Fig. 2. The location of three major hatcheries of chum salmon centrations of elements to be detected by the analytical in Korea (Yangyang, Samchuk, and Uljin). The rearing water instrument. Water samples were also collected from the and otoliths of hatchery-reared chum salmon fry were col- hatcheries in spring 2001 and 2002 (Table 1). Water was lected from these hatcheries in the spring of 2001 and 2002. filtered through a 0.45 µm membrane filter using a vacuum pump, and 0.5 ml of nitric acid was added to each 100 ml aliquot of filtered water. 1999). Recently, interest in otolith microchemistry for At least nine elements (Ca, Na, Mg, Al, Cu, Sr, Ba, stock separation has increased because the analytical ca- Mn, and Zn) in both otoliths and rearing water were mea- pability of instruments has improved the precision and sured using inductively coupled plasma mass accuracy of measurements. For example, before the 1980s spectrometry (ICP-MS; X7 model, Thermo Elevertcal only six papers on otolith microchemistry had been pub- Ltd.) at the Korea Basic Science Institute. Filtered and lished, but the number of publications in this field in- acidified water samples were directly nebulized into the creased rapidly in the 1990s (Campana and Thorrold, instrument using a standard pneumatic nebulization sys- 2001). The inner ear of teleost fish contains three pairs of tem. Preparation of a standard solution for external cali- otoliths (earstones): the sagittae, lapilli and asterisci. Most bration was done using the EPA Method 5010. The signal scientists use sagittae for analysis of otolith elements drift and matrix effects were corrected using internal because they are the largest of the otoliths. Fish otoliths standards of 103Rh and 205Tl 10 ng/ml solution. Weighed have a role in balancing and hearing, and grow through- otolith samples were transferred into teflon vials and dis- out the entire life span of the fish. Fish otoliths consist of solved with several drops of purified concentrated nitric ~96% calcium carbonate (CaCO ), 3% protein complex, acid. The solution was diluted with Milli-Q water (18.2 3 and ~1% minor and trace elements, including radioiso- M ohm) on a balance to an appropriate mass (~3 g). Dis- topes and stable isotopes (Campana, 1999). The chemi- solved metals in rearing water were analyzed using the cal composition of otoliths does not change after forma- same methods. The concentration of all elements was tion (Campana and Neilson, 1985); therefore, many re- normalized by the calcium concentration, and the mean searchers believe the chemical composition of fish otoliths value and standard deviation at each site was calculated. can describe stock structure and migration routes and have Using the equation W = aLb, where W is body weight potential as environmental indicators, natural tags, or el- and L is fork length, we established a relationship be- 306 D. Sohn et al. Table 1. Description of samples collected from three study areas on the east coast of the Korean Peninsula during (a) spring 2001 and (b) spring 2002. (a) Study area Sampling date Sample size Fork length Body weight Otolith length (cm) (g) (µm) Yangyang Hatchery Otolith 2001 March 5 6.1 ± 0.4 1.3 ± 0.1 — Water 2001 June 3 Samchuk Hatchery Otolith 2001 March 8 5.7 ± 0.3 1.3 ± 0.3 — Water 2001 June 2 Uljin Hatchery Otolith 2001 March 13 8.2 ± 0.8 3.9 ± 1.2 — Water 2001 June 2 (b) Study area Sampling date Sample size Fork length Body weight Otolith length (cm) (g) (µm) Yangyang Hatchery Otolith 2002 March 280 4.3 ± 0.3 1.0 ± 0.2 8.5 ± 0.4 Water 2002 March 2 Samchuk Hatchery Otolith 2002 March 266 5.5 ± 0.3 2.2 ± 0.3 9.9 ± 0.7 Water 2002 March 3 Uljin Hatchery Otolith 2002 March 303 7.7 ± 0.7 5.3 ± 1.3 13.1 ± 1.1 Water 2002 March 2 tween fork length and body weight from samples collected in March 2002. Analysis of covariance (ANCOVA) was : W=0.009L3.20 used to assess geographical differences in salmon fry : W=0.024L2.63 growth. The mean values of element concentrations in : W=0.026L2.60 the otoliths and water were compared among the three study sites. Analysis of variance (ANOVA) was used to assess geographical differences in otolith elemental con- centrations. Discriminant analysis was used to place salmon into groups based on the ratios of eight elements to calcium. All statistical analyses were carried out using the STATISTICA program. 3. Results Fig. 3. The relationship between fork length and body weight There was a large difference in growth rate among of chum salmon fry collected from the three study areas in the hatcheries, even though salmon fry from all of the March 2002. hatcheries were similar in age. Fry from the southernmost location, Uljin, were the biggest and those from the north- ernmost, Yangyang, were the smallest. The means and between fork length and body weight of chum salmon fry standard deviations (SDs) of fry fork lengths collected in were W = 0.026L2.60, W = 0.024L2.63, and W = 0.009L3.20 the spring of 2002 were 4.3 ± 0.3, 5.5 ± 0.3, and 7.6 ± 0.7 for Yangyang, Samchuk, and Uljin, respectively (Fig. 3). cm for Yangyang, Samchuk, and Uljin, respectively. The The length and weight data were log transformed and means and SDs of body weight were 1.0 ± 0.2, 2.2 ± 0.3, analyzed using ANCOVA. The null hypothesis of the test and 5.3 ± 1.3 g (Table 1), and the means and SDs of the was that the slopes of the lines are the same in all the length of the longitudinal axis of otoliths were 8.5 ± 0.4, groups. ANCOVA analysis revealed geographically dif- 9.9 ± 0.7, and 13.1 ± 1.1, respectively. The relationships ferent growth patterns, with significant relationships be- Salmon Stock Identification Using Trace Elements in Otoliths 307 Table 2. Results of the ANCOVA for the relationship between fork length and body weight of chum salmon fry in the three study areas. Source DF MS F p Fork length 1 11.34 5700.211 0.0000 Sampling areas 2 0.174 87.533 0.0001 Error 843 1.985E-03 Total 847 Table 3. Molar ratios between elements and Ca in the otoliths of chum salmon fry collected on March 2001. Study area Na/Ca Mg/Ca Al/Ca Mn/Ca Cu/Ca Zn/Ca Sr/Ca Ba/Ca mmol/mol mmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol Yangyang 13.87 2.79 385.77 7.74 7.45 247.07 1535.86 9.64 Samchuk 13.02 2.81 24.60 1.82 2.76 82.38 172.97 0.73 Uljin 14.55 1.29 124.24 8.62 5.92 256.36 830.30 3.63 Table 4. Ratios of eight elements to Ca in the rearing water of salmon fry collected from the east coast of Korea in June 2001. 2001 June Na/Ca Mg/Ca Mn/Ca Sr/Ca Ba/Ca Cu/Ca Zn/Ca Al/Ca Rearing water mmol/mol mmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol Yangyang 2784.1 415.4 394.1 4821.4 575.2 574.2 1212.3 3164.7 2741.1 414.0 376.6 5120.5 554.6 267.5 2312.6 2573.7 2713.1 417.8 378.8 5114.1 561.9 306.4 2421.7 3613.1 Mean 2746.4 415.7 383.2 5018.7 563.9 382.7 1982.2 3117.1 *SD 35.4 1.9 9.5 668.9 10.4 167.0 668.9 521.3 Samchuk 169.6 103.3 91.7 1247.5 135.1 65.2 563.4 627.0 163.7 102.5 88.9 1200.3 131.9 71.9 568.3 848.0 Mean 166.6 102.9 90.3 1223.9 133.5 68.5 565.9 737.5 SD 4.2 0.6 2.0 33.4 2.3 4.8 3.5 156.2 Uljin 1124.1 350.2 745.6 1911.9 143.0 222.1 2541.2 847.5 770.5 295.7 570.1 1844.5 102.4 172.4 722.3 378.6 Mean 947.3 323.0 657.8 1878.2 122.7 197.3 1631.7 613.0 SD 250.0 38.5 124.1 47.7 28.7 35.1 1286.1 331.6 *SD: Standard deviation. tween fork length and body weight of chum salmon fry size, we could only get one data point for each element. in the study areas (F = 87.533, p < 0.0001; Table 2). Us- Elemental concentrations in fry otoliths were generally ing all of the data collected, the length-weight relation- high from Yangyang fry. Sr/Ca, Ba/Ca, Al/Ca, and Cu/Ca ship for fry was derived as W = 0.0144L2.90 (r2 = 0.98). ratios were the highest from the Yangyang hatchery and We believe that temperature differences of rearing water second highest from Uljin. Although Na/Ca, Mn/Ca, and at the study areas may have resulted in the differences Zn/Ca ratios were highest from the Uljin hatchery, the among fry lengths. Unfortunately, we could not compare ratios from Yangyang were nearly as high. On the other temperatures because hatcheries did not keep tempera- hand, the ratios of most elements to Ca, except for Mg/ ture records. Ca, were lowest in Samchuk. The Mg/Ca ratio was the Elemental signatures indicated that the chemical highest in Samchuk hatchery (Table 3). composition of fry otoliths were distinctly different in Otolith samples collected in 2002 also showed dif- the three study areas. In 2001, due to the small sample ferences in chemical composition among geographical 308 D. Sohn et al. Fig. 4. Mean and standard deviation of the concentration ratios of eight elements to Ca in otoliths of chum salmon fry and in rearing water collected at the three study areas in March 2002. Vertical bars represent one standard deviation. groups. Although the absolute concentrations of elements In spring 2001, nine element concentrations in rear- were not the same as in 2001, there were many similari- ing water were measured (Ca, Na, Mg, Al, Mn, Cu, Zn, ties between two years. Sr/Ca and Ba/Ca ratios were the Sr, and Ba). The ratios of these elements to Ca indicated highest in Yangyang fry, and Mg/Ca and Na/Ca were high- that most elements in rearing water were in higher con- est in Samchuk fry. Other elemental ratios (Mn/Ca, Zn/ centrations in Yangyang and Uljin than in Samchuk (Ta- Ca, Al/Ca, and Cu/Ca) were highest in Uljin fry. ANOVA ble 4). When we compare the ratios in the water with the was used to assess the difference in elemental composi- ratios from otoliths, regional variation was evident and tions and significant variation among the study sites was some elements in water were well reflected in otoliths. found in some elemental signatures (Mg/Ca, Na/Ca, Sr/ Sr/Ca, Mn/Ca, and Cu/Ca ratios were selected as good Ca, Ba/Ca, and Mn/Ca), while no statistical differences indicator elements because the concentration of these el- were detected for Zn/Ca, Al/Ca, and Cu/Ca ratios (Fig. ements was in the same order in otoliths and in rearing 4). As found in the 2001 samples, Sr/Ca and Ba/Ca ratios water (Fig. 5). Elemental signatures indicated that the were significantly higher in otoliths from Yangyang than chemical composition of rearing water collected in March in those from Samchuk and Uljin (Sr/Ca, F = 9075.5, p < 2002 was also distinctly different with respect to the 0.00001; Ba/Ca, F = 615.65, p < 0.00001). However, Mg/ hatchery locations. In March 2002, all element ratios ex- Ca and Na/Ca ratios were the highest in Samchuk otoliths cept Mn/Ca and Mg/Ca were highest in Yangyang water and Mn/Ca, Zn/Ca, Al/Ca, and Cu/Ca ratios were the high- and all element ratios except Ba/Ca and Al/Ca were low- est in Uljin otoliths. est in Samchuck water. In 2002, Sr/Ca, Ba/Ca, and Mn/ Salmon Stock Identification Using Trace Elements in Otoliths 309 Fig. 6. The first two axes of discriminant analysis using the concentration ratios of eight elements to Ca in otoliths to distinguish stock and natal origin of chum salmon fry from the east coast of Korea. nant analysis. Discriminant analysis of the ratios of eight elements to Ca (Na/Ca, Mg/Ca, Al/Ca, Cu/Ca, Sr/Ca, Ba/ Ca, Mn/Ca, and Zn/Ca) showed a distinct separation be- tween stock natal areas (Fig. 6). The clearest discrimina- tion was for Yangyang salmon, by the first canonical variate. The second canonical variate separated Samchuk and Uljin salmon almost completely. Fig. 5. Sr/Ca, Mn/Ca, and Cu/Ca ratios in rearing water col- lected in June 2001 (right panels) and the otoliths of reared 4. Discussion chum salmon fry collected in March 2001 (left panels). Because of the lack of experimental information, we were not able to completely explain the relationship be- tween environmental factors and salmon growth. How- Ca ratios were in the same concentration orders in otoliths ever, salmon fry of the same age were different in size and in rearing water (Fig. 4). among the three hatcheries, and the difference may be Comparing the chemical composition of otoliths in due to temperature differences among the hatcheries be- chum salmon fry with the chemical composition of their cause the three hatcheries are located at different latitudes. rearing water demonstrated the power of this analysis for Yangyang is the northernmost, while Uljin is the separating stocks from different geographic habitats. The southernmost. Peterson et al. (1977) reported that the data from both years showed that some elemental con- length of Atlantic salmon (Salmo salar) alevins increased centrations in otoliths and rearing water varied geographi- as temperature increased. Though information on water cally. Sr/Ca and Ba/Ca ratios, in particular, showed simi- temperature was not available from the hatcheries, it lar geographical variation patterns, although their abso- makes intuitive sense that the highest temperature was lute concentrations were different. For example, Sr/Ca found in the south (i.e., Uljin) and the lowest in the north ratios of rearing water were highest in Yangyang (4504 (i.e., Yangyang). µmol/mol) and lowest in Samchuk (515 µmol/mol). Re- Two basic assumptions about the chemistry of sults from the otolith analysis showed the highest Sr/Ca otoliths were made in this study: that otolith chemistry ratios at Yangyang (1378 µmol/mol) and the lowest at reflects that of the environment in which they were formed Samchuk (494 µmol/mol). Sr/Ca ratios in water and and that otolith chemistry is area-specific. Though the otoliths appeared to have a linear relationship. The Sr/Ca specific environmental factors that affect the microchem- ratio in otoliths varied depending on the concentration in istry of otoliths is still unknown, this research demon- water, regardless of locality and timing. This may sug- strated that chemical characteristics of otoliths did vary gest that element chemistry of otoliths in salmon responds among habitats. In addition to the effect of the environ- to the chemistry of the salmon’s rearing water. ment in which they are formed, it has been shown that The multivariate classification of elemental concen- the microchemical composition of otoliths is influenced trations was reduced to two dimensions using discrimi- by physiological processes (Brown and Harris, 1995; 310 D. Sohn et al. Table 5. Ratios of eight elements to Ca in the rearing water of salmon fry collected from the east coast of Korea in March 2002. 2002 March Na/Ca Mg/Ca Mn/Ca Sr/Ca Ba/Ca Cu/Ca Zn/Ca Al/Ca Rearing water mmol/mol mmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol µmol/mol Yangyang 1182.4 273.7 178.2 4478.4 547.5 80.1 260.0 801.6 1140.0 275. 9 167.5 4530.2 557.9 55.6 124.4 625.3 Mean 1161.2 274.8 172.8 4504.3 552.7 67.9 192.2 713.4 *SD 30.0 1.6 7.5 36.6 7.3 17.3 95.8 124.6 Samchuk 166.9 99.1 16.6 510.5 33.4 30.5 1033.9 112.4 154.1 99.4 11.4 513.3 29.1 21.1 301.4 72.8 160.5 99.4 14.9 522.2 29.4 22.7 436.8 119.6 Mean 160.5 99.3 14.3 515.4 30.6 24.8 590.7 101.6 SD 6.4 0.2 2.7 6.1 2.4 5.0 389.7 25.2 Uljin 957.0 310.9 3019.3 1835.8 134.8 43.7 176.7 217.3 920.6 307.7 2956.0 1828.2 130.2 30.7 67.5 110.7 Mean 938.8 309.3 2987.7 1832.0 132.5 37.2 122.1 164.0 SD 25.7 2.3 44.8 5.3 3.3 9.2 77.2 75.4 *SD: Standard deviation. Schroder et al., 1995), water temperature (Townsend et characteristics. For instance, the values of oxygen (δ18O), al., 1995), diet (Limburg, 1995; Gallahar and Kingsford, carbon (δ13C), and nitrogen (δ15N) isotopes from 1996), age and stress (Kalish, 1989). foraminifera fossils and fish otoliths have been measured If the elemental concentrations in streams stay con- to distinguish habitat temperature, paleoclimatic data stant over a long enough time interval, otolith micro- (Grossman and Ku, 1986), ecological positions of fish chemistry can help in identifying different natal areas. (Sugisaki and Tsuda, 1995), life cycle characteristics (Gao Our results showed that the chemical composition of rear- and Beamish, 1999) and age (Campana and Jones, 1998). ing water was distinctly different among the three hatch- Both isotopes and REEs are multi-use proxies that can be eries. Sr/Ca and Ba/Ca ratios in otoliths and rearing wa- used to identify different stocks and trace the relation- ters were stable for two years, and Sr/Ca and Ba/Ca ra- ship of otoliths with physical characteristics of the envi- tios in rearing water seemed to be especially well reflected ronment, such as salinity and temperature. in the otoliths of salmon fry. Therefore, we could sepa- In this study, after comparing and analyzing the rate stocks of chum salmon fry from the three study areas microchemistry of salmon otoliths, we found that the based on these ratios in otoliths. Other studies have also chemistry of the ambient water affects the chemical com- reported that some elements could be used to identify fish position of the otoliths. This is a powerful relationship stocks or populations among habitats. Limburg (1995) that can be used to separate salmon stocks by hatchery or described the use of Sr to separate habitat areas that var- natal area. Using this technique to distinguish the origins ied with climate and geography. Rooker et al. (2001) sepa- of wild-caught salmon at sea will be important in the fu- rated bluefin tuna stocks into eastern and western nurs- ture because it could help mitigate international conflicts ery grounds based on Sr/Ca and Ba/Ca ratios in otoliths. over fisheries. The chemical analysis of core portions of And Patterson et al. (1999) explained geographical dif- adult otoliths may show a pattern of microchemistry simi- ferences in immature Nassau grouper (Epinephelus lar to fry otoliths from the same origin. More study is striatus) within a 180 km range using Zn/Ca, Sr/Ca, Ba/ needed to determine the partition coefficients for elemen- Ca, and Pb/Ca ratios in otoliths. Likewise, our study clas- tal ratios such as Sr/Ca and Ba/Ca in order to clarify the sified three study areas within 55–140 km of the east coast relationship between rearing water and otoliths. of Korea using concentrations of several elements. Al- though the study areas are near each other, the areas do Acknowledgements vary in the ratios of concentrations of elements such as We would like to express our special thanks to sci- Na/Ca, Sr/Ca, Ba/Ca, Mg/Ca, and Mn/Ca in rearing wa- entists on the Salmon Research Team of National Fisher- ter and otoliths. ies Research and Development Institute, Samchuck In- New techniques using other isotopes and rare earth land Development Station, and Uljin Research Center for elements (REEs) may help identifying habitat and stock Freshwater Fish for the collection of salmon fry otoliths. Salmon Stock Identification Using Trace Elements in Otoliths 311 This study was jointly supported by the Ministry of Sci- Kalish, J. M. (1989): Otolith microchemistry: validation of the ence and Technology (Project: Fluctuations of marine liv- effects of physiology, age and environment on otolith com- ing resources in response to marine environmental vari- position. J. Exp. Mar. Biol. Ecol., 132, 151–178. ability) and the National Oceanic & Atmospheric Admin- Limburg, K. E. (1995): Otolith strontium traces environmental history of subyearling American shad Alosa sapidissima. istration (NOAA) of the USA (Personal Research con- Mar. Ecol. Prog. Ser., 119, 25–35. tract: AB133F-02-SE-1331). Patterson, H. M., S. R. Thorrold and J. M. Shenker (1999): Analysis of otolith chemistry in Nassau grouper References (Epinephelus striatus) from the Bahamas and Belize using Begg, G. A. and J. R. Waldman (1999): An holistic approach to solution-based ICP-MS. Coral Reef, 18, 171–178. fish stock identification. Fish. Res., 43, 35–44. Peterson, R. H., H. C. E. Spinney and A. Sreedharan (1977): Brown, P. and J. H. Harris (1995): Strontium batch-marking of Development of Atlantic salmon (Salmo salar) eggs and golden perch (Macquaria ambigua Richardson) and trout alevins under varied temperature regimes. J. Fish. Res. cod (Maccullochella macquariensis) (Cuvier). p. 693–701. Board Can., 34, 31–43. In Recent Developments in Fish Otolith Research, ed. by Rooker, J. R., D. H. Secor, V. S. Zdanowicz and T. Itoh (2001): D. H. Secor, J. M. Dean and S. E. Campana, University of Discrimination of northern bluefin tuna from nursery areas South Carolina Press, Columbia, SC. in the Pacific Ocean using otolith chemistry. Mar. Ecol. Campana, S. E. (1999): Chemistry and composition of fish Prog. Ser., 218, 275–282. otoliths: pathways, mechanisms and applications. Mar. Ecol. Rooker, J. R., D. H. Secor, V. S. Zdanowicz, G. D. Metrio, L. Prog. Ser., 188, 263–297. O. Relini, M. Deflorio, N. Santamaria, G. Palandri and M. Campana, S. E. and C. M. Jones (1998): Radiocarbon from Relini (2002): Otolith elemental fingerprints of Atlantic nuclear testing applied to age validation of black drum, bluefin tuna from eastern and western nurseries. Col. Vol. Pogonias cromis. Fish. Bull., 96, 185–192. Sci. Pap. ICCAT, 54, 198–506. Campana, S. E. and J. D. Neilson (1985): Microstructure of Schroder, S. L., C. M. Knudsen and E. C. Volk (1995): Mark- fish otoliths. Can. J. Fish. Aquat. Sci., 42, 1014–1032. ing salmon fry with strontium chloride solutions. Can. J. Campana, S. E. and S. R. Thorrold (2001): Otoliths, increments, Fish. Aquat. Sci., 52, 1141–1149. and elements: keys to a comprehensive understanding of Seong, K. B. (1999): Biological characteristics and population fish populations? Can. J. Fish. Aquat. Sci., 58, 30–38. genetics of salmonid species from Korea. Ph.D. Disserta- Campana, S. E., J. A. Gagn and J. W. McLaren (1995): Elemen- tion, Pukyoung National University, 125 pp. (in Korean). tal fingerprinting of fish otoliths using ID-ICPMS. Mar. Sugisaki, H. and A. Tsuda (1995): Nitrogen and carbon stable Ecol. Prog. Ser., 122, 115–120. isotopic ecology in the ocean: The transportation of organic Gallahar, N. K. and M. J. Kingsford (1996): Factors influenc- materials through the food web. p. 307–317. In ing Sr/Ca ratios in otoliths of Girella elevata: an experi- Biogeochemical Processes and Ocean Flux in the Western mental investigation. J. Fish. Biol., 48, 174–186. Pacific, ed. by H. Sakai and Y. Nozaki, TERRAPUB, To- Gao, Y. W. and R. J. Beamish (1999): Isotopic composition of kyo. otoliths as a chemical tracer in population identification of Thorrold, S. R., C. M. Jones and S. E. Campana (1997): Re- sockeye salmon (Oncorhynchus nerka). Can. J. Fish. Aquat. sponse of otolith microchemistry to environmental varia- Sci., 56, 2062–2068. tions experienced by larval and juvenile Atlantic croaker Gillanders, B. M. and M. J. Kingsford (2000): Elemental fin- (Micropogonias undulatus). Limnol. Oceanogr., 42, 102– gerprints of otoliths of fish may distinguish estuarine ‘nurs- 111. ery’ habitats. Mar. Ecol. Prog. Ser., 201, 273–286. Thorrold, S. R., C. M. Jones, S. E. Campana, J. W. Mclaren and Groot, C. and L. Margolis (1991): Pacific Salmon Life Histo- J. W. H. Lam (1998): Trace element signatures in otoliths ries. UBC Press, Vancouver, Canada, 564 pp. record natal river of juvenile American shad (Alosa Grossman, E. L. and T. L. Ku (1986): Oxygen and carbon iso- sapidissima). Limnol. Oceanogr., 43, 1826–1835. tope fractionation in biogenic aragonite: temperature effects. Thresher, R. E. (1999): Elemental composition of otoliths as a Chemical Geology (Isotope Geoscience Section), 59, 59– stock delineator in fishes. Fish. Res., 43, 165–204. 74. Townsend, D. W., R. L. Radtke, S. Corwin and D. A. Libby Jung, W., Y. H. Lee, S. Kim, D. H. Jin and K. B. Seong (2003): (1995): Strontium:calcium ratios for hindcasting larval cod Genetic identification of the North Pacific Chum Salmon Gadus morhua distributions relative to water masses on (Oncorhynchus keta) stocks. J. Kor. Fish. Soc., 36, 578– Georges Bank. Mar. Ecol. Prog. Ser., 119, 37–44. 585. 312 D. Sohn et al.

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