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Using otolith trace elements as biological tracer for tracking larval dispersal of black porgy, Acanthopagrus schlegeli and yellowfin seabream, A. latus among estuaries of western Taiwan

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Abstract

To understand if the trace elements in the otoliths can be used as a biological tracer for tracking natal origin and dispersal of larval black porgy (Acanthopagrus schlegeli) and yellowfin seabream (A. latus) among estuaries, the fish larvae in 1997, 1998, and 2005 and water samples in 2005 were collected from 3 estuaries on the western coast of Taiwan. The elemental composition in both otoliths of the larvae and water samples were analyzed by a solution-based inductively coupled plasma mass spectrometer (ICP-MS). Temporal and spatial differences were found in some of the measured 12 element/Ca ratios in the larval otoliths. The water elemental composition was also significantly different between estuaries and between flood and ebb tides. 87.5–100 % of the larvae of both species could be successfully assigned to their sampled estuaries. However, only 20 % of the black porgy collected from TT in 1998 could be successfully assigned to TT and the rest to GST and TK. The low assignment might be due to the mixing by the tidal current because the flood tide comes from the direction of TK in the south and GST in the north and merged in the middle of Taiwan Strait nearby TT. This study demonstrated that the trace elements in the otoliths of the fish have the potential to detect the temporal and spatial variation of environmental conditions in the estuaries and subsequently can be used for tracking the origin of the larvae from different estuaries and their dispersal rate.

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References

  • Abu-Hakima R (1984) Some aspects of the reproductive biology of Acanthopagrus spp. (Family: Sparidae). J Fish Biol 25:515–526

    Article  Google Scholar 

  • Akazaki M, Takito A (1982) Studies on the seedling reproduction of yellowfin porgy (Kichinu). Acanthopagrus latus Houttuyn, 2: Egg development and metamorphosis of larvae. Aqua 29(4):218–228

    Google Scholar 

  • Alibert C, Kinsley L, Fallon SJ, McCulloch MT, Berkelmans R, McAllister F (2003) Source of trace element variability in Great Barrier Reef corals affected by the Burdekin flood plumes. Geochimica et cosmochimica acta 67:231–246

    Article  CAS  Google Scholar 

  • Bath GE, Thorrold SR, Jone CM, Campana SE, McLaren JW, Lam JWH (2000) Strontium and barium uptake in aragonitic otoliths of marine fish. Geochimica et cosmochimica acta 64:1705–1714

    Article  CAS  Google Scholar 

  • Brophy D, Jeffries TE, Danilowicz BS (2004) Elevated manganese concentrations at the cores of clupeid otoliths: possible environmental, physiological, or structural origins. Mar Biol 144:779–786

    Article  CAS  Google Scholar 

  • Brown P, Harris JH (1995) Strontium batch- marking of golden perch (Macquaria ambigua Richardson) and trout cod (Maccullochella macquariensis Cuvier). In: Secor DH, Dean JM, Campana SE (eds) Recent developments in fish otolith research. University of South Carolina Press, Columbia, pp 693–701

    Google Scholar 

  • Brown AL, Busby MS, Mier KL (2001) Walleye pollock Theragra chalcogramma during transformation from the larval to juvenile stage: otolith and osteological development. Mar Biol 139(5):845–851

    Article  Google Scholar 

  • Bruland KW (1983) Trace elements in sea-water. Chem Oceano 8:157–220

    CAS  Google Scholar 

  • Campana SE (1999) Chemistry and composition of fish otoliths: pathway, mechanisms and applications. Mar Ecol Prog Ser 188:263–297

    Article  CAS  Google Scholar 

  • Campana SE, Gagne JA, Mclaren JW (1995) Elemental fingerprinting of fish otoliths using ID-ICPMS. Mar Ecol Prog Ser 122:115–120

    Article  Google Scholar 

  • Chang CW, Hsu CC, Wang YT, Tzeng WN (2002) Early life history of Acanthopagrus latus and A. schegeli (Sparidae) on the western coast of Taiwan: temporal and spatial partitioning of recruitment. Mar Fresh Res 53:411–417

    Article  Google Scholar 

  • Chang MY, Wang CH, You CF, Tzeng WN (2006) Individual-based dispersal patterns of larval gobies in an estuary as indicated by otolith elemental fingerprints. Sci Mar 70:165–174

    CAS  Google Scholar 

  • Chang MY, Tzeng WN, Wang CH, You CF (2008) Rhinogobius giurinus among estuaries of western Taiwan: Implication for comprehending the larval dispersal and metapopulation connectance. Zool Stud 47(6):676–684

    Google Scholar 

  • Chu TY (1963) The oceanography of the surrounding waters of Taiwan. Inst Fish Bio Taiwan Univ 1(4):29–39

    Google Scholar 

  • Dove SG, Gillanders BM, Kingsford MJ (1996) An investigation of chronological differences in the deposition of trace metals in the otoliths of two temperate reef fishes. J Exp Mar Biol Ecol 205:15–33

    Article  CAS  Google Scholar 

  • Elsdon TS, Gillanders BM (2003) Relationship between water and otolith elemental concentrations in juvenile fish, Acanthopagrus butcheri. Mar Ecol Prog Ser 260:263–272

    Article  CAS  Google Scholar 

  • Elsdon TE, Gillanders BM (2005) Alternative life-history patterns of estuarine fish: Barium in otoliths elucidates freshwater residency. Can J Fish Aqua Sci 62:1143–1152

    Article  CAS  Google Scholar 

  • Everitt B (1978) Graphical techniques for multivariate data. Heinemann, London

    Google Scholar 

  • Farrell J, Campana SE (1996) Regulation of calcium and strontium deposition on the otolith of juvenile tilapia, Oreochromis niloticus. Comp Biochem Physiol 115:103–109

    Article  Google Scholar 

  • Forrester GE (2005) A field experiment testing for correspondence between trace elements in otoliths and the environment and for evidence of adaptation to prior habitats. Estuar 28(6):974–981

    Article  CAS  Google Scholar 

  • Fowler AJ, Campana SE, Jones CM, Torrold SR (1995) Experimental assessment of the effect of temperature and salinity on elemental composition of otoliths using solution-based ICPMS. Can J Fish Aqua Sci 52:1421–1430

    Article  Google Scholar 

  • Fukuhara O (1987) Larval development and behavior in early life stages of black sea bream reared in the laboratory. Nippon Suisan Gakk 53:371–379

    Article  Google Scholar 

  • Gillanders BM, Kinsford MJ (2003) Spatial variation in elemental composition of otoliths of three species of fish (family Sparidae). Estuar Coast Shelf Sci 57:1049–1064

    Article  CAS  Google Scholar 

  • Gillanders BM, Able KW, Brown JA, Eggleston DB, Sheeidan PF (2003) Evidence of connectivity between juvenile and adult habitats for mobile marine fauna: An important component of nurseries. Mar Ecol Prog Ser 247:281–295

    Article  Google Scholar 

  • Hoff GR, Fuiman LA (1995) Environmentally induced variation in elemental composition of red drum (Sciaenops ocellatus) otoliths. Bull Mar Sci 56:578–591

    Google Scholar 

  • Jean CT, Lee SC, Chen TC (1992) Morphometric studies on the fishes of subfamily Sparinae (Perciformes: Sparidae) from the coastal waters of Taiwan. J Fish Soc Tai 19:231–238

    Google Scholar 

  • Kafemann R, Adlerstein S, Neukamm R (2000) Variation in otolith strontium and calcium ratios as an indicator of life history strategies of freshwater species within a brackish water system. Fish Res 46:313–325

    Article  Google Scholar 

  • Kennedy BD, Folt CL, Blum JD, Chamberlain CP (1997) Natural isotope markers in salmon. Nature 387:766–767

    Article  CAS  Google Scholar 

  • Kennedy BP, Blum JD, Folt CL, Nislow KH (2000) Using natural strontium isotopic signatures as fish markers: methodology and application. Can J Fish Aqua Sci 57:2280–2292

    Article  CAS  Google Scholar 

  • Kennedy BP, Klaue A, Blum JD, Folt CL, Nislow KH (2002) Reconstructing the lives of fish using Sr isotopes in otoliths. Can J Fish Aqua Sci 59:925–929

    Article  Google Scholar 

  • Leu MY (1994) Natural spawning and larval rearing of silver sea bream, Rhabdosargus sarba (ForskaÊl), in captivity. Aqua 120:115–122

    Article  Google Scholar 

  • Liao IC (1997) Aquaculture practices in Taiwan and its visions. J Fish Soc Tai 32(3):193–206

    Google Scholar 

  • Mihelakakis A, Kitajima C (1995) Spawning of the silver sea bream, Sparus sarba, in captivity. Jap J Ichthy 42:53–59

    Google Scholar 

  • Milton DA, Chenery SR (2001) Sources and uptake of trace metal in otoliths of juvenile barramundi (Lates calcarifer). J Exp Mar Biol Ecol 264:47–65

    Article  CAS  Google Scholar 

  • Pollock BR, Weng H, Morton RM (1983) The seasonal occurrence of postlarval stages of yellowfin bream, Acanthopagrus australis (GuÈnther), and some factors affecting their movement into an estuary. J Fish Biol 22:409–415

    Article  Google Scholar 

  • Rieman BE, Myers DL, Nielsen RL (1994) Use of otolith microchemistry to discriminate Oncorhynchus nerka of resident and anadromous origin. Can J Fish Aqua Sci 51:68–77

    Article  CAS  Google Scholar 

  • Ruttenberg BJ, Warner RW (2006) Spatial variation in the chemical composition of natal otoliths from reef fish in the Galapagos Islands. Mar Ecol Prog Ser 328:225–236

    Article  CAS  Google Scholar 

  • Ruttenburg BJ, Hamilton SL, Hickford MJH, Paradis GC, Sheehy MS, Standish JD, Tzvi OB, Warner RR (2005) Elevated levels of trace elements in cores of otoliths and their potential for use as natural tags. Mar Ecol Prog Ser 297:273–281

    Article  Google Scholar 

  • Schroder S, Knudsen C, Volk E (1995) Marking salmon fry with strontium chloride solutions. Can J Fish Aqua Sci 52:1141–1149

    Article  CAS  Google Scholar 

  • Secor DH, Rooker JR, Zlokovitz E, Zdanowicz VS (2001) Indentification of riverine, estuarine, and coastal contingents of Hudson River striped bass based upon otolith elemental fingerprints. Mar Ecol Prog Ser 211:245–253

    Article  CAS  Google Scholar 

  • Swearer SE, Forrester GE, Steele MA, Brooks AJ, Lea DW (2003) Spatio-temporal and interspecific variation in otolith trace-elemental fingerprints in a temperate estuarine fish assemblages. Estuar Coast Shel Sci 56:1111–1123

    Article  CAS  Google Scholar 

  • Thorrold SR, Latkoczy C, Swart PK, Jones CM (2001) Natal homing in a marine fish metapopulation. Sci (Wash., D. C.) 291:297–299

    Google Scholar 

  • Thresher RE (1999) Elemental composition of otoliths as a stock delineator in fishes. Fish Res 43:165–204

    Article  Google Scholar 

  • Tzeng WN (1996) Effects of salinity and ontogenetic movements on strontium: calcium ratios in the otoliths of the Janpanese eel, Anguilla japonica. J Exp Mar Biol Ecol 199:111–122

    Article  CAS  Google Scholar 

  • Tzeng WN, Tsai YC (1994) Changes in otolith microchemistry of Japanese eel, Anguilla japonica, during its migration from the ocean to the rivers of Taiwan. J Fish Biol 45:671–683

    Google Scholar 

  • Tzeng WN, Wang YT, Chang CW (2002) Spatial and Temporal variations of the estuarine larval fish community on the west coast of Taiwan. Mar Fresh Res 53(2):419–430

    Article  Google Scholar 

  • Tzeng WN, Chang CW, Wang CH, Shiao JC, Iizuka Y, Yang YJ, You CF, Lŏzys L (2007) Misidentification of the migratory history of anguillid eels by Sr/Ca ratios of vaterite otoliths. Mar Ecol Prog Ser 348:285–295

    Article  CAS  Google Scholar 

  • Volk EC, Schroder SL, Grimm JJ (1999) Otolith thermal marking. Fish Res 43(1–3):205–219

    Article  Google Scholar 

  • Wells BK, Rieman BE, Clayton JL, Horan DL, Jones CM (2003) Relationships between water, otolith, and scale chemistries of westslope cutthroat trout from the Coeur d’ Alene River, Idaho: the potential application of hard-part chemistry to describe movements in freshwater. Trans Amer Fish Soc 132:409–424

    Article  CAS  Google Scholar 

  • Williams BK, Titus K (1988) Assessment of sampling stability in ecological applications of discriminant analysis. Ecol 69(4):1275–1285

    Article  Google Scholar 

  • Zenitani H, Kimura R (2007) Elemental analysis of otoliths of otoliths of Japanese anchovy: trial to discriminate between Seto Inland Sea and Pacific stock. Fish Sci 73:1–8

    Article  CAS  Google Scholar 

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Acknowledgments

This study was financially supported by the Council of Agriculture, Republic of China (Project No. COA 96AS-14.1.1-FA-F1). The authors are grateful to the previous students and research assistants of Fisheries Biology lab of the Department of Zoology (the present Department of Life science), National Taiwan University for the field sampling work, and also to Yu-Tzu Wang for the larvae species identification.

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Authors and Affiliations

  1. Biodiversity Center, Academia Sinica, Taipei, Taiwan, Republic of China

    Mei-Yu Chang

  2. Institute of Fisheries Sciences, College of Life Science, National Taiwan University, Taipei, Taiwan, Republic of China

    Wann-Nian Tzeng

  3. Department of Environmental Biology and Fisheries Science, National Taiwan Ocean University, Keelung, Taiwan, Republic of China

    Wann-Nian Tzeng

  4. Department of Earth Sciences, National Cheng Kung University, Tainan, Taiwan, Republic of China

    Chen-Fong You

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  1. Mei-Yu Chang
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  2. Wann-Nian Tzeng
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  3. Chen-Fong You
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Correspondence to Wann-Nian Tzeng.

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Chang, MY., Tzeng, WN. & You, CF. Using otolith trace elements as biological tracer for tracking larval dispersal of black porgy, Acanthopagrus schlegeli and yellowfin seabream, A. latus among estuaries of western Taiwan. Environ Biol Fish 95, 491–502 (2012). https://doi.org/10.1007/s10641-012-0081-7

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  • DOI: https://doi.org/10.1007/s10641-012-0081-7

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