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Fully Equipped to Succeed: Migratory Contingents Seen as an Intrinsic Potential for Striped Bass to Exploit a Heterogeneous Environment Early in Life

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Abstract

Migratory contingents, groups of individuals belonging to the same population that adopt different migratory patterns, have been identified in numerous Striped Bass (Morone saxatilis) populations along North American East Coast. We tested the hypothesis that migratory contingents may develop early in life to maximize the exploitation of the variety of habitats faced by a recently introduced fish population. Using the discriminatory power provided by otolith chemistry, we studied early-life history stages of Striped Bass in a recently reintroduced population in the St. Lawrence Estuary. Migratory patterns were inferred using multivariate analysis of four otolith trace elements (Sr, Ba, Mn, and Mg) on juveniles (0+ and 1+). Three migratory contingents were identified during early-life history stages: freshwater residents, oligohaline migrants, and mesohaline migrants. This study demonstrates the rapid establishment, in less than 10 years since initial stocking, of three migratory contingents initiated early in life among the St. Lawrence Striped Bass population. We postulate that diversification provided by the establishment of distinct migratory contingents among early-life history stages promotes the rapid colonization of new environments through the exploration and exploitation of an increased number of nursery habitats.

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References

  • Arai T., A. Kotake, and K. Morita. 2004. Evidence of downstream migration of Sakhalin taimen, Hucho perryi, as revealed by Sr:Ca ratios of otolith. Ichthyological Research 51: 377–380.

    Article  Google Scholar 

  • Bewers J.M., and P.A. Yeats. 1978. Trace metals in the waters of a partially mixed estuary. Estuarine and Coastal Marine Science 7: 147–162.

    Article  CAS  Google Scholar 

  • Bulger A.J., B.P. Hayden, M.E. Monaco, D.M. Nelson, and M.G. McCormick-Ray. 1993. Biologically-based estuarine salinity zones derived from a multivariate analysis. Estuaries 16: 311–322.

    Article  Google Scholar 

  • Campana S.E. 1990. How reliable are growth back-calculations based on otoliths?. Canadian Journal of Fisheries and Aquatic Sciences 47: 2219–2227.

    Article  Google Scholar 

  • Campana S.E. 1999. Chemistry and composition of fish otoliths: pathways, mechanisms and applications. Marine Ecology Progress Series 188: 263–297.

    Article  CAS  Google Scholar 

  • Campana S.E. 2005. Stock identification methods: application in fishery science. In Otolith elemental composition as a natural marker of fish stocks, eds. S.X. Cadrin, K.D. Friedland, and J.R. Waldman, 719. Amsterdam: Elsevier Academic Press.

    Google Scholar 

  • Campana S.E., J.A. Gagne, and J.W. McLaren. 1995. Elemental fingerprinting of fish otoliths using ID-ICPMS. Marine Ecology Progress Series 122: 115–120.

    Article  Google Scholar 

  • Chapman B.B., C. Brönmark, J.-Å. Nilsson, and L.-A. Hansson. 2011a. The ecology and evolution of partial migration. Oikos 120: 1764–1775.

    Article  Google Scholar 

  • Chapman B.B., C. Brönmark, J.-Å. Nilsson, and L.-A. Hansson. 2011b. Partial migration: an introduction. Oikos 120: 1761–1763.

    Article  Google Scholar 

  • Chapman B.B., K. Hulthén, J. Brodersen, P.A. Nilsson, C. Skov, L.A. Hansson, and C. Brönmark. 2012. Partial migration in fishes: causes and consequences. Journal of Fish Biology 81: 456–478.

    Article  CAS  Google Scholar 

  • Clark J. 1968. Seasonal movements of Striped Bass contingents of Long Island Sound and the New York Bight. Transactions of the American Fisheries Society 97: 320–343.

  • Cossa D., and S.A. Poulet. 1978. Survey of trace metal contents of suspended matter in the St. Lawrence Estuary and Saguenay Fjord. Journal of the Fisheries Research Board of Canada 35: 338–345.

    Article  CAS  Google Scholar 

  • Dauvin J.-C., and J.J. Dodson. 1990. Relationship between feeding incidence and vertical and longitudinal distribution of rainbow smelt larvae (Osmerus mordax) in a turbid well-mixed estuary. Marine Ecology Progress Series 60: 1–12.

    Article  Google Scholar 

  • Dickey C.L., J.J. Isely, and J.R. Tomasso. 1997. Slow growth did not decouple the otolith size–fish size relationship in Striped Bass. Transactions of the American Fisheries Society 126: 1027–1029.

    Article  Google Scholar 

  • Dodson J.J., J.-C. Dauvin, R.G. Ingram, and B. d’Anglejan. 1989. Abundance of larval rainbow smelt (Osmerus mordax) in relation to the maximum turbidity zone and associated macroplanktonic fauna of the middle St. Lawrence estuary. Estuaries and Coasts 12: 66–81.

    Article  Google Scholar 

  • Dodson, J.J., N. Aubin-Horth, V. Thériault, and D.J. Paez. 2013. The evolutionary ecology of alternative migratory tactics in salmonid fishes. Biological Reviews.

  • Douglas S.G., G. Chaput, J. Hayward, and J. Sheasgreen. 2009. Prespawning, spawning, and postspawning behavior of Striped Bass in the Miramichi River. Transactions of the American Fisheries Society 138: 121–134.

    Article  Google Scholar 

  • Eldridge M.B., J.A. Whipple, D. Eng, M.J. Bowers, and B.M. Jarvis. 1981. Effects of food and feeding factors on laboratory-reared Striped Bass larvae. Transactions of the American Fisheries Society 110: 111–120.

    Article  Google Scholar 

  • Eldridge M.B., J.A. Whipple, and M.J. Bowers. 1982. Bioenergetics and growth of Striped Bass, Morone saxatilis, embryos and larvae. Fishery Bulletin 80: 461–474.

    Google Scholar 

  • Elsdon T.S., and B.M. Gillanders. 2005. Alternative life-history patterns of estuarine fish: barium in otoliths elucidates freshwater residency. Canadian Journal of Fisheries and Aquatic Sciences 62: 1143–1152.

    Article  CAS  Google Scholar 

  • Elsdon T.S., and B.M. Gillanders. 2006. Identifying migratory contingents of fish by combining otolith Sr:Ca with temporal collections of ambient Sr:Ca concentrations. Journal of Fish Biology 69: 643–657.

    Article  CAS  Google Scholar 

  • Gemperline, P.J., R.A. Rulifson, and L. Paramore. 2002. Multi-way analysis of trace elements in fish otoliths to track migratory patterns. Chemometrics and Intelligent Laboratory Systems 60: 135–146.

  • Hanson J.M., and S.C. Courtenay. 1995. Water, science and the public: the Miramichi ecosystem. In Seasonal abundance and distribution of fishes in the Miramichi estuary, ed. M.P. Chadwick. Moncton: Canadian Special Publication of Fisheries and Aquatic Sciences.

    Google Scholar 

  • Hedger R.D., P.M. Atkinson, I. Thibault, and J.J. Dodson. 2008. A quantitative approach for classifying fish otolith strontium: calcium sequences into environmental histories. Ecological Informatics 3: 207–217.

    Article  Google Scholar 

  • Hjort J. 1914. Fluctuations in the great fisheries of northern Europe. Rapports et procès-verbaux - ICES 20: 237.

    Google Scholar 

  • Hughes A.L. 2012. Evolution of adaptive phenotypic traits without positive Darwinian selection. Heredity 108: 347–353.

    Article  CAS  Google Scholar 

  • Jessop B.M., J.C. Shiao, Y. Iizuka, and W.N. Tzeng. 2002. Migratory behaviour and habitat use by American eels Anguilla rostrata as revealed by otolith microchemistry. Marine Ecology Progress Series 233: 217–229.

    Article  Google Scholar 

  • Jonsson B., and N. Jonsson. 1993. Partial migration: niche shift versus sexual maturation in fishes. Reviews in Fish Biology and Fisheries 3: 348–365.

    Article  Google Scholar 

  • Kalish J.M. 1990. Use of otolith microchemistry to distinguish the progeny of sympatric anadromous and non-anadromous salmonids. Fishery Bulletin 88: 657–666.

    Google Scholar 

  • Kerr L.A., D.H. Secor, and P.M. Piccoli. 2009. Partial migration of fishes as exemplified by the estuarine-dependent white perch. Fisheries 34: 114–123.

    Article  Google Scholar 

  • Lazartigues A.V., P. Sirois, and D. Savard. 2014. LA-ICP-MS analysis of small samples: carbonate reference materials and larval fish otoliths. Geostandards and Geoanalytical Research 30: 225–240.

    Google Scholar 

  • Lecomte F., O. Morissette, G. Verreault, M. Legault, and P. Sirois. unpubl. Long time no see: the successful re-introduction of Striped Bass at the northern-most extend of its distributional range (St. Lawrence Estuary, Canada). Québec: Chaire de recherche MRNF sur les espèces aquatiques exploitées.

  • Lindley S.T., D.L. Erickson, M.L. Moser, G. Williams, O.P. Langness, B.W. McCovey, M. Belchik, D. Vogel, W. Pinnix, J.T. Kelly, J.C. Heublein, and A.P. Klimley. 2011. Electronic tagging of green sturgeon reveals population structure and movement among estuaries. Transactions of the American Fisheries Society 140: 108–122.

    Google Scholar 

  • Mansueti, R.J. 1958. Eggs, larvae and young of the Striped Bass, Roccus saxatilis. In Chesapeake biological laboratory contribution 112. Solomons: Chesapeake Biological Laboratory.

  • Martino E.J., and E.D. Houde. 2010. Recruitment of Striped Bass in Chesapeake Bay: spatial and temporal environmental variability and availability of zooplankton prey. Marine Ecology-Progress Series 409: 213–228.

    Article  Google Scholar 

  • Mercier L., D. Mouillot, O. Bruguier, L. Vigliola, and A.M. Darnaude. 2012. Multi-element otolith fingerprints unravel sea-lagoon lifetime migrations of gilthead sea bream Sparus aurata. Marine Ecology Progress Series 444: 175–194.

    Article  Google Scholar 

  • Morais P., E. Dias, J. Babaluk, and C. Antunes. 2011. The migration patterns of the European flounder Platichthys flesus (Linnaeus, 1758) (Pleuronectidae, Pisces) at the southern limit of its distribution range: ecological implications and fishery management. Journal of Sea Research 65: 235–246.

    Article  Google Scholar 

  • Nordeng H. 1983. Solution to the “char problem” based on Arctic char (Salvelinus alpinus) in Norway. Canadian Journal of Fisheries and Aquatic Sciences 40: 1372–1387.

    Article  Google Scholar 

  • North E.W., and E.D. Houde. 2003. Linking ETM physics, zooplankton prey, and fish early-life histories to Striped Bass Morone saxatilis and white perch M. americana recruitment (vol 260, pg. 219, 2003). Marine Ecology-Progress Series 264: 219–236.

    Article  Google Scholar 

  • Pelletier A.-M., G. Bourget, M. Legault, and G. Verreault. 2011. Réintroduction du bar rayé (Morone saxatilis) dans le fleuve Saint-Laurent: Bilan du rétablissement de l’espèce. Naturaliste Canadien 135: 79–85.

    Google Scholar 

  • Peterson R.H., D.J. Martin-Robichaud, and Å. Berge. 1996. Influence of temperature and salinity on length and yolk utilization of Striped Bass larvae. Aquaculture International 4: 89–103.

    Article  Google Scholar 

  • Phillis C.C., D.J. Ostrach, B.L. Ingram, and P.K. Weber. 2011. Evaluating otolith Sr/Ca as a tool for reconstructing estuarine habitat use. Canadian Journal of Fisheries and Aquatic Sciences 68: 360–373.

    Article  CAS  Google Scholar 

  • Pulido F. 2011. Evolutionary genetics of partial migration—the threshold model of migration revis(it) ed. Oikos 120: 1776–1783.

    Article  Google Scholar 

  • Quinn G.P., and M.J. Keough. 2002. Experimental design and data analysis for biologists. Cambridge: Cambridge University press.

    Book  Google Scholar 

  • R Core Team. 2012. R: a language and environment for statistical computing. Vienna: R foundation for statistical computing.

    Google Scholar 

  • Ray G.C. 2005. Connectivities of estuarine fishes to the coastal realm. Estuarine, Coastal and Shelf Science 64: 18–32.

    Article  Google Scholar 

  • Robichaud-LeBlanc K.A., S.C. Courtenay, and T.J. Benfey. 1998. Distribution and growth of young-of-the-year Striped Bass in the Miramichi River estuary, Gulf of St. Lawrence. Transactions of the American Fisheries Society 127: 56–69.

    Article  Google Scholar 

  • Robinson M., S. Courtenay, T. Benfey, L. Maceda, and I. Wirgin. 2004. Origin and movements of young-of-the-year Striped Bass in the southern Gulf of St. Lawrence, New Brunswick. Transactions of the American Fisheries Society 133: 412–426.

    Article  Google Scholar 

  • Robitaille, J., M. Bérubé, A. Gosselin, M. Baril, J. Beauchamp, J. Boucher, S. Dionne, M. Legault, Y. Mailhot, B. Ouellet, P. Sirois, S. Tremblay, G. Trencia, G. Verreault, and D. Villeneuve. 2011. Recovery strategy for the Striped Bass (Morone saxatilis), St. Lawrence Estuary population, Canada. In Species at risk act recovery strategy series, xi +51. Ottawa: Fisheries and Oceans Canada.

  • Rooker J.R., D.H. Secor, V.S. Zdanowicz, and T. Itoh. 2001. Discrimination of northern bluefin tuna from nursery areas in the Pacific Ocean using otolith chemistry. Marine Ecology Progress Series 218: 275–282.

    Article  CAS  Google Scholar 

  • Rossiter, D.G. 2013. Technical note: optimal partitioning of soil transects with R Version 2.1, 26 pp.

  • Rulifson R.A., and M.J. Dadswell. 1995. Life history and population characteristics of Striped Bass in Atlantic Canada. Transactions of the American Fisheries Society 124: 477–507.

    Article  Google Scholar 

  • Secor D.H. 1992. Application of otolith analysis to investigate anadromy in Chesapeake Bay Striped Bass Morone saxatilis. Fishery Bulletin 90: 798–806.

    Google Scholar 

  • Secor D.H. 1999. Specifying divergent migrations in the concept of stock: the contingent hypothesis. Fisheries Research 43: 13–34.

    Article  Google Scholar 

  • Secor D.H., and J.M. Dean. 1989. Somatic growth effects on the otolith—fish size relationship in young pond-reared Striped Bass, Morone saxatilis. Canadian Journal of Fisheries and Aquatic Sciences 46: 113–121.

    Article  Google Scholar 

  • Secor D.H., and P.M. Piccoli. 1996. Age- and sex-dependent migrations of Striped Bass in the Hudson River as determined by chemical microanalysis of otoliths. Estuaries 19: 778–793.

    Article  CAS  Google Scholar 

  • Secor D.H., and P.M. Piccoli. 2007. Oceanic migration rates of Upper Chesapeake Bay Striped Bass (Morone saxatilis), determined by otolith microchemical analysis. Fishery Bulletin 105: 62–73.

    Google Scholar 

  • Secor D.H., A. Henderson-Arzapalo, and P.M. Piccoli. 1995. Can otolith microchemistry chart patterns of migration and habitat utilization in anadromous fishes?. Journal of Experimental Marine Biology and Ecology 192: 15–33.

    Article  Google Scholar 

  • Secor D.H., J.R. Rooker, E.R. Zlokovitz, and V.S. Zdanowicz. 2001. Identification of riverine, estuarine and coastal contingents of Hudson River Striped Bass based upon otolith elemental fingerprints. Marine Ecology Progress Series 211: 245–253.

    Article  CAS  Google Scholar 

  • Sirois P., and J.J. Dodson. 2000. Critical periods and growth-dependent survival of larvae of an estuarine fish, the rainbow smelt Osmerus mordax. Marine Ecology Progress Series 203: 233–245.

    Article  Google Scholar 

  • Smith S.E., and S. Kato. 1979. San Francisco bay: the urbanized estuary. In The fisheries of San Francisco bay: past, present and future, ed. T.J. Conomos, 445–468. San Francisco: Pacific Division of the American Association for the Advancement of Science.

    Google Scholar 

  • St. Lawrence Centre. 1996. Synthesis report on the state of the St. Lawrence River. Volume 1: the St. Lawrence ecosystem. Montréal: Environment Canada.

    Google Scholar 

  • Stevens D.E., D.W. Kohlhorst, L.W. Miller, and D.W. Kelley. 1985. The decline of Striped Bass in the Sacramento-San Joaquin Estuary, California. Transactions of the American Fisheries Society 114: 12–30.

    Article  Google Scholar 

  • Subramanian V., and B. D’Anglejan. 1976. Water chemistry of the St. Lawrence estuary. Journal of Hydrology 29: 341–354.

    Article  CAS  Google Scholar 

  • Tabachnick B., and L. Fidell. 1996. Using multivariate statistics, 3rd edn. New York: Harper & Row.

    Google Scholar 

  • Tsai C.-F. 1991. Prey density requirements of the Striped Bass, Morone saxatilis (Walbaum), larvae. Estuaries 14: 207–217.

    Article  Google Scholar 

  • Tsukamoto K., I. Nakai, and W.-V. Tesch. 1998. Do all freshwater eels migrate?. Nature 396: 635–636.

    Article  CAS  Google Scholar 

  • Tzeng W.N., J.C. Shiao, and Y. Iizuka. 2002. Use of otolith Sr:Ca ratios to study the riverine migratory behaviors of Japanese eel Anguilla japonica. Marine Ecology Progress Series 245: 213–221.

    Article  Google Scholar 

  • Volk E.C., D.L. Bottom, K.K. Jones, and C.A. Simenstad. 2010. Reconstructing juvenile chinook salmon life history in the Salmon River Estuary, Oregon, using otolith microchemistry and microstructure. Transactions of the American Fisheries Society 139: 535–549.

    Article  Google Scholar 

  • Wallus R., and T.P. Simon. 2006. Reproductive biology and early life history in the Ohio River drainage. Boca Raton: CRC Press.

    Book  Google Scholar 

  • Webster R. 1973. Automatic soil-boundary location from transect data. Mathematical Geology 5: 27–37.

    Article  Google Scholar 

  • Wingate R.L., D.H. Secor, and R.T. Kraus. 2011. Seasonal patterns of movement and residency by Striped Bass within a subestuary of the Chesapeake Bay. Transactions of the American Fisheries Society 140: 1441–1450.

    Article  Google Scholar 

  • Yeats P.A., and D.H. Loring. 1991. Dissolved and particulate metal distributions in the St. Lawrence estuary. Canadian Journal of Earth Sciences 28: 729–742.

    Article  CAS  Google Scholar 

  • Zimmerman C.E., and G.H. Reeves. 2002. Identification of steelhead and resident rainbow trout progeny in the Deschutes River, Oregon, revealed with otolith microchemistry. Transactions of the American Fisheries Society 131: 986–993.

    Article  Google Scholar 

  • Zimmerman C.E., P.S. Rand, M. Fukushima, and S.F. Zolotukhin. 2012. Migration of Sakhalin taimen (Parahucho perryi): evidence of freshwater resident life history types. Environmental Biology of Fishes 93: 223–232.

    Article  Google Scholar 

  • Zlokovitz E.R., D.H. Secor, and P.M. Piccoli. 2003. Patterns of migration in Hudson River Striped Bass as determined by otolith microchemistry. Fisheries Research 63: 245–259.

    Article  Google Scholar 

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Acknowledgments

We thank Anne-Marie Pelletier, Kim Belzile, Patrick Gagnon, and Annie Marquis from Ministère des Forêts, de la Faune et des Parcs for sampling of Striped Bass in the St. Lawrence River. We also thank Dany Savard, Angélique Lazartigues, Sadia Mehdi, and Anne-Lise Fortin from the Université du Québec à Chicoutimi for the lab work. Comments and suggestions from Julian J. Dodson and Laure Devine for language revision of a manuscript’s earlier version are also acknowledged.

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Correspondence to Olivier Morissette.

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Morissette, O., Lecomte, F., Verreault, G. et al. Fully Equipped to Succeed: Migratory Contingents Seen as an Intrinsic Potential for Striped Bass to Exploit a Heterogeneous Environment Early in Life. Estuaries and Coasts 39, 571–582 (2016). https://doi.org/10.1007/s12237-015-0015-7

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