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Contrasting Seascape Use by a Coastal Fish Assemblage: a Multi-methods Approach

  • Ronald Baker
  • Adam Barnett
  • Michael Bradley
  • Katya Abrantes
  • Marcus Sheaves
Article
  • 35 Downloads

Abstract

Understanding the range of habitats needed to complete life-cycles is essential for the effective conservation and management of species. We combined otolith microchemistry, acoustic tracking, and underwater video to determine patterns of seascape use by an assemblage of tropical snappers, including two little-known species of high economic importance, the Papuan black bass (Lutjanus goldiei) and spot-tail snapper (Lutjanus fuscescens). All species appeared to have marine larval phases, and post-settlement distributions broadly overlapped across the coastal seascape. However, species and life stages were distributed along a gradient from freshwater to coastal waters. Lutjanus fuscescens is primarily a freshwater species post-settlement, but larger individuals move into brackish estuaries and even coastal waters at times. Lutjanus goldiei appear to recruit to low salinity or freshwater areas. Larger individuals tend to have home-ranges centred on brackish estuaries, while making regular movements into both coastal waters and freshwater. Lutjanus argentimaculatus also ranged widely from fresh to coastal waters, but juveniles were most common in the saline parts of estuaries. Ontogenetic shifts by L. argentimaculatus were similar to those reported from other regions, despite vast differences in the spatial proximity of seascape components. The wide-ranging seascape movements of our target species highlight the importance of maintaining effective connectivity between marine, estuarine, and freshwaters in the region to maintain ecosystem function and support sustainable sport fisheries. The combined approaches resolved some of the ambiguities of individual methods and provide a powerful approach to understanding seascape use by coastal fishes.

Keywords

Ontogeny Connectivity Otolith microchemistry Acoustic tracking Underwater video 

Notes

Acknowledgements

We thank Riccard and Nathalie Reimann of Baia Sportfishing and the people of Baia Village for their support of this research, Lina Pandihau of the Papua New Guinea National Fisheries Authority for assistance with field work and logistical planning, Dr. Yi Hu of the Advanced Analytical Centre at JCU for training and advice on LA-ICPMS, and Mark O’Callaghan for advice on the preparation of otoliths for analysis.

Author Contributions

All authors designed the study and collected the samples; MB sectioned and aged otoliths, and conducted LA-ICPMS; RB analysed the otolith microchemistry data; AB analysed the acoustic tracking data; MB conducted and analysed the underwater video census; RB wrote the paper with input from all authors.

Funding Information

This research was funded by the Papua New Guinea National Fisheries Authority and the Australian Centre for International Agricultural Research under grant FIS-2013-015. RB was partly supported by a fellowship from the Tropical Landscapes Joint Venture between the Commonwealth Scientific and Industrial Research Oganisation and James Cook University.

Compliance with Ethical Standards

Field work was conducted in collaboration with and permission of the Papua New Guinea National Fisheries Authority. All applicable institutional and national guidelines for the care and use of animals were followed, and this work was completed in accordance with JCU’s animal ethics guidelines under JCU Ethics Permit A2308.

Conflict of Interest

The authors declare they have no conflict of interest.

Supplementary material

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References

  1. Allen, G.R. 1985. An annotated and illustrated catalogue of lutjanid species known to date. FAO species catalogue, Vol. 6. Snappers of the World. FAO, Rome.Google Scholar
  2. Allen, G.R. 2004. A review of the freshwater fish fauna of the trans Fly ecoregion. Report to World Wildlife Fund South Pacific program, Suva. In Fiji.Google Scholar
  3. Arthington, A., R. Naiman, M. McClain, and C. Nilsson. 2010. Preserving biodiversity and ecological services of rivers: new challenges and research opportunities. Freshwater Biology 55: 1–16.CrossRefGoogle Scholar
  4. Baker, R., M. Bradley, S. Freddi, K. Abrantes, A. Barnett, and M. Sheaves. 2018. Non-lethal aging of tropical catch-and-release sport fishery species. Fisheries Research 207: 110–117.CrossRefGoogle Scholar
  5. Barnett, A., K.G. Abrantes, R. Baker, A. Diedrich, A. Kuilboer, T. Mahony, I. McLeod, G. Moscardo, M. Prideaux, A. van Luyn, and M. Sheaves. 2016. Sport fisheries, conservation, and sustainable livelihoods: a multidisciplinary assessment of best practice. Fish and Fisheries 17: 696–713.CrossRefGoogle Scholar
  6. Beck, M., K. Heck, K. Able, D. Childers, D. Eggleston, B. Gillanders, B. Halpern, C. Hays, K. Hoshino, T. Minello, R. Orth, P. Sheridan, and M. Weinstein. 2001. The identification, conservation, and management of estuarine and marine nurseries for fish and invertebrates. Bioscience 51: 633–641.CrossRefGoogle Scholar
  7. Biggs, C.R., and R.S. Nemeth. 2014. Timing, size, and duration of a Dog (Lutjanus jocu) and Cubera Snapper (Lutjanus cyanopterus) spawning aggregation in the U.S. Virgin Islands. Proceedings of the Gulf and Caribbean Fisheries Institute 67: 240–245.Google Scholar
  8. Bradley, M., R. Baker, and M. Sheaves. 2017. Hidden components in tropical seascapes: deep-estuary habitats support unique fish assemblages. Estuaries and Coasts 40: 1195–1206.CrossRefGoogle Scholar
  9. Brophy, D., T.E. Jeffries, and B.S. Danilowicz. 2004. Elevated manganese concentrations at the cores of clupeid otoliths: possible environmental, physiological, or structural origins. Marine Biology 144: 779–786.CrossRefGoogle Scholar
  10. Brown, R., and K. Severin. 2009. Otolith chemistry analyses indicate that water Sr:Ca is the primary factor influencing otolith Sr:Ca for freshwater and diadromous fish but not for marine fish. Canadian Journal of Fisheries and Aquatic Science 66: 1790–1808.CrossRefGoogle Scholar
  11. Caddy, J. 2008. The importance of “cover” in the life histories of demersal and benthic marine resources: a neglected issue in fisheries assessment and management. Bulletin of Marine Science 83: 7–52.Google Scholar
  12. Campana, S. 1999. Chemistry and composition of fish otoliths: pathways, mechanisms and applications. Marine Ecology Progress Series 188: 263–297.CrossRefGoogle Scholar
  13. Cappo, M., P. Eden, S.J. Newman, and S. Robertson. 2000. A new approach to validation of periodicity and timing of opaque zone formation in the otolith of eleven species of Lutjanus from the central Great Barrier Reef. Fishery Bulletin 98: 474–488.Google Scholar
  14. Cappo, M., R. Marriott, and S. Newman. 2013. James’s rule and causes and consequences of a latitudinal cline in the demography of John’s Snapper (Lutjanus johnii) in coastal waters of Australia. Fishery Bulletin 111: 309–324.CrossRefGoogle Scholar
  15. Choat, J.H., J.P. Kritzer, and J.L. Ackerman. 2009. Aging in coral reef fishes: Do we need to validate the periodicity of increment formation of every species of fish for which we collect age-based demographic data? In: Green, B.S., Mapstone B.D., Carlos G., Begg G.A. (Eds) 2009. Tropical fish otoliths: information for assessment, management and ecology. Reviews: Methods and Technologies in Fish Biology and Fisheries, Vol. 11.Google Scholar
  16. Cocheret de la Moriniere, E., B.I.A. Pollux, I. Nagelkerken, and G. van der Velde. 2002. Post-settlement life cycle migration patterns and habitat preference of coral reef fish that use seagrass and mangrove habitats as nurseries. Estuarine Coastal and Shelf Science 55: 309–321.CrossRefGoogle Scholar
  17. Crook, D.A., D.J. Buckle, Q. Allsop, W. Baldwin, T.M. Saunders, P.M. Kyne, J.D. Woodhead, R. Maas, B. Roberts, and M.M. Douglas. 2017. Use of otolith chemistry and acoustic telemetry to elucidate migratory contingents in barramundi Lates calcarifer. Marine and Freshwater Research 68: 1554–1566.CrossRefGoogle Scholar
  18. Dorenbosch, M., M.C. Verweij, I. Nagelkerken, N. Jiddawi, and G. van der Velde. 2004. Homing and daytime tidal movements of juvenile snappers (Lutjanidae) between shallow-water nursery habitats in Zanzibar, western Indian Ocean. Environmental Biology of Fishes 70: 203–209.CrossRefGoogle Scholar
  19. Dahlgren, C.P., and D.B. Eggleston. 2000. Ecological processes underlying ontogenetic habitat shifts in a coral reef fish. Ecology 81: 2227–2240.CrossRefGoogle Scholar
  20. Elsdon, T., and B. Gillanders. 2003. Recontructing migratory patterns of fish based on environmental influences on otolith chemistry. Reviews in Fish Biology and Fisheries 13: 219–235.CrossRefGoogle Scholar
  21. Elsdon, T., and B. Gillanders. 2005. Consistency of patterns between laboratory experiments and field collected fish in otolith chemistry: an example and applications for salinity reconstructions. Marine and Freshwater Research 56: 609–617.CrossRefGoogle Scholar
  22. Elsdon, T., B. Wells, S. Campana, B. Gillanders, C. Jones, K. Limburg, D. Secor, S. Thorrold, and B. Walther. 2008. Otolith chemistry to describe movements and life-history parameters of fishes: hypotheses, assumptions, limitations and inferences. Oceanography and Marine Biology: An Annual Review 46: 297–330.Google Scholar
  23. Fodrie, F.J., L.A. Yeager, J.H. Grabowski, C.A. Layman, G.D. Sherwood, and M.D. Kenworthy. 2015. Measuring individuality in habitat use across complex landscapes: approaches, constraints, and implications for assessing resource specialization. Oecologia 178: 75–87.CrossRefGoogle Scholar
  24. Froese, R., and D. Pauly. 2017. Editors, FishBase. World Wide Web electronic publication. www.fishbase.org, version (06/2017).
  25. Garratt, P.A. 1993. Spawning of riverbream, Acanthopagrus berda, in Kosi estuary. South African Journal of Zoology 28: 26–31.CrossRefGoogle Scholar
  26. Gillanders, B.M. 2005. Otolith chemistry to determine movements of diadromous and freshwater fish. Aquatic Living Resources 18: 291–300.CrossRefGoogle Scholar
  27. Gillanders, B., K. Able, J. Brown, D. Eggleston, and P. Sheridan. 2003. Evidence of connectivity between juvenile and adult habitats for mobile marine fauna: an important component of nurseries. Marine Ecology Progress Series 247: 281–295.CrossRefGoogle Scholar
  28. Hamer, P., A. Henderson, M. Hutchinson, J. Kemp, C. Green, and P. Feutry. 2015. Atypical correlation of otolith strontium: Calcium and barium: calcium across a marine-freshwater life history transition of a diadromous fish. Marine and Freshwater Research 66: 411–419.CrossRefGoogle Scholar
  29. Hammerschlag-Peyer, C.M., and C.A. Layman. 2010. Intrapopulation variation in habitat use by two abundant coastal fish species. Marine Ecology Progress Series 415: 211–220.CrossRefGoogle Scholar
  30. Keith, P., C. Lord, and K. Maeda. 2015. Indo-Pacific Sicydiine Gobies. Biodiversity, life traits and conservation. 256p. Societe Francaise d’Ichtyologie, Paris, France.Google Scholar
  31. Kimirei, I.A., I. Nagelkerken, B. Griffioen, C. Wagner, and Y.D. Mgaya. 2011. Ontogenetic habitat use by mangrove/seagrass-associated coral reef fishes shows flexibility in time and space. Estuarine Coastal and Shelf Science 92: 47–58.CrossRefGoogle Scholar
  32. Luo, J.G., J.E. Serafy, S. Sponaugle, P.B. Teare, and D. Kieckbusch. 2009. Movement of gray snapper Lutjanus griseus among subtropical seagrass, mangrove, and coral reef habitats. Marine Ecology Progress Series 380: 255–269.CrossRefGoogle Scholar
  33. Matich, P., J.S. Ault, R.E. Boucek, D.R. Bryan, K.R. Gastrich, C.L. Harvey, M.R. Heithaus, J.J. Kiszka, V. Paz, J.S. Rehage, and A.E. Rosenblatt. 2017. Ecological niche partitioning within a large predator guild in a nutrient-limited estuary. Limnology and Oceanography 62: 934–953.CrossRefGoogle Scholar
  34. Mateo, I., E.G. Durbin, R.S. Appeldoorn, A.J. Adams, F. Juanes, R. Kingsley, P. Swart, and D. Durant. 2010. Role of mangroves as nurseries for French Grunt Haemulon flavolineatum and schoolmaster Lutjanus apodus assessed by otolith elemental fingerprints. Marine Ecology Progress Series 402: 197–212.CrossRefGoogle Scholar
  35. McCulloch, M., M. Cappo, J. Aumend, and W. Muller. 2005. Tracing the life history of individual barramundi using laser ablation MC-ICP-MS Sr-isotopic and Sr/Ba ratios in otoliths. Marine and Freshwater Research 56: 637–644.CrossRefGoogle Scholar
  36. Nagelkerken, I., M. Sheaves, R. Baker, and R.M. Connolly. 2015. The seascape nursery: a novel spatial approach to identify and manage nurseries for coastal marine fauna. Fish and Fisheries 16: 362–371.CrossRefGoogle Scholar
  37. Nagelkerken, I., M. Dorenbosch, W. Verberk, E.C. de la Moriniere, and G. van der Velde. 2000. Importance of shallow-water biotopes of a Caribbean bay for juvenile coral reef fishes: patterns in biotope association, community structure and spatial distribution. Marine Ecology Progress Series 202: 175–192.CrossRefGoogle Scholar
  38. Nakamura, Y., M. Horinouchi, T. Shibuno, Y. Tanaka, T. Miyajima, I. Koike, H. Kurokura, and M. Sano. 2008. Evidence of ontogenetic migration from mangroves to coral reefs by black-tail snapper Lutjanus fulvus: stable isotope approach. Marine Ecology Progress Series 355: 257–266.CrossRefGoogle Scholar
  39. O’Connor, J.J., D. Lecchini, H.J. Beck, G. Cadiou, G. Lecellier, D.J. Booth, and Y. Nakamura. 2016. Sediment pollution impacts sensory ability and performance of settling coral-reef fish. Oecologia 180: 11–21.CrossRefGoogle Scholar
  40. Oka, S., and K. Tachihara. 2008. Migratory history of the spotted flagtail, Kuhlia marginata. Environmental Biology of Fishes 81: 321–327.CrossRefGoogle Scholar
  41. Piddocke, T., G. Butler, P. Butcher, S. Purcell, D. Bucher, and L. Christidis. 2015. Age validation in the Lutjanidae: a review. Fisheries Research 167: 48–63.CrossRefGoogle Scholar
  42. Russell, D.J., and A.J. McDougall. 2005. Movement and juvenile recruitment of mangrove jack, Lutjanus argentimaculatus (Forsskal), in northern Australia. Marine and Freshwater Research 56: 465–475.CrossRefGoogle Scholar
  43. Ruttenberg, B., S. Hamilton, M. Hickford, G. Paradis, M. Sheehy, J. Standish, O. Ben-Tzvi, and R. Warner. 2005. Elevated levels of trace elements in cores of otoliths and their potential for use as natural tags. Marine Ecology Progress Series 297: 273–281.CrossRefGoogle Scholar
  44. Sadovy, Y. 2016. Mainstreaming fish spawning aggregations into fishery management calls for a precautionary approach. Bioscience 66: 295–306.CrossRefGoogle Scholar
  45. Secor, D.H. 1999. Specifying divergent migrations in the concept of stock: the contingent hypothesis. Fisheries Research 43 (1–3): 13–34.CrossRefGoogle Scholar
  46. Sheaves, M. 1995. Large lutjanid and serranid fishes in tropical estuaries: are they adults or juveniles? Marine Ecology Progress Series 129: 31–40.CrossRefGoogle Scholar
  47. Sheaves, M., and B. Molony. 2000. Short-circuit in the mangrove food chain. Marine Ecology Progress Series 199: 97–109.CrossRefGoogle Scholar
  48. Sheaves, M., B. Molony, and A. Tobin. 1999. Spawning migrations and local movements of a tropical sparid fish. Marine Biology 133: 123–128.CrossRefGoogle Scholar
  49. Sheaves, M., R. Baker, I. Nagelkerken, and R.M. Connolly. 2015. True value of estuarine and coastal nurseries for fish: incorporating complexity and dynamics. Estuaries and Coasts 38: 401–414.CrossRefGoogle Scholar
  50. Sheaves, M., R. Baker, I. McLeod, K. Abrantes, J. Wani, and A. Barnett. 2016. The conservation status of Niugini black bass: a world-renowned sport fish with an uncertain future. Fisheries Management and Ecology 23: 243–252.CrossRefGoogle Scholar
  51. Snover, M.L. 2008. Ontogenetic habitat shifts in marine organisms: influencing factors and the impact of climate variability. Bulletin of Marine Science 83: 53–67.Google Scholar
  52. Swales, S., A. Storey, and K. Bakowa. 2000. Temporal and spatial variations in fish catches in the Fly River system in Papua New Guinea and the possible effects of the Ok Tedi copper mine. Environmental Biology of Fishes 57: 75–95.CrossRefGoogle Scholar
  53. Tanaka, K., Y. Hanamura, V. Chong, S. Watanabe, A. Man, F. Kassim, M. Kodama, and T. Ichikawa. 2011. Stable isotope analysis reveals ontogenetic migration and the importance of a large mangrove estuary as a feeding ground for juvenile John’s snapper Lutjanus johnii. Fisheries Science 77: 809–816.CrossRefGoogle Scholar
  54. Thorrold, S.R., G.P. Jones, S. Planes, and J.A. Hare. 2006. Transgenerational marking of embryonic otoliths in marine fishes using barium stable isotopes. Canadian Journal of Fisheries and Aquatic Sciences 63: 1193–1197.CrossRefGoogle Scholar
  55. Travers, M., I. Potter, K. Clarke, S. Newman, and J. Hutchins. 2010. The inshore fish faunas over soft substrates and reefs on the tropical west coast of Australia differ and change with latitude and bioregion. Journal of Biogeography 37: 148–169.CrossRefGoogle Scholar
  56. Verweij, M.C., I. Nagelkerken, K.E.M. Hol, A.H.J.B. van den Beld, and G. van der Velde. 2007. Space use of Lutjanus apodus including movement between a putative nursery and a coral reef. Bulletin of Marine Science 81: 127–138.Google Scholar
  57. Walther, B.D., and K.E. Limburg. 2012. The use of otolith chemistry to characterize diadromous migrations. Journal of Fish Biology 81: 796–825.CrossRefGoogle Scholar
  58. Wood, A., J. Butler, M. Sheaves, and J. Wani. 2013. Sport fisheries: opportunities and challenges for diversifying coastal livelihoods in the Pacific. Marine Policy 42: 305–314.CrossRefGoogle Scholar

Copyright information

© Coastal and Estuarine Research Federation 2018

Authors and Affiliations

  • Ronald Baker
    • 1
    • 2
    • 3
  • Adam Barnett
    • 1
  • Michael Bradley
    • 1
    • 2
  • Katya Abrantes
    • 1
    • 2
  • Marcus Sheaves
    • 1
    • 2
  1. 1.Marine Biology and Aquaculture Unit, College of Science and EngineeringJames Cook UniversityTownsvilleAustralia
  2. 2.TropWATERJames Cook UniversityTownsvilleAustralia
  3. 3.University of South Alabama, Dauphin Island Sea LabDauphin IslandUSA

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