Femtosecond laser ablation ICP-MS measurement of otolith Sr:Ca and Ba:Ca composition reveal differential use of freshwater habitats for three amphidromous Sicyopterus (Teleostei: Gobioidei: Sicydiinae) species

Journal of Fish Biology

Volumn 79, Issue 5, 2011, Pages 1304-1321

  Lord, C ^a,b   Tabouret, H ^b,c   Claverie, F ^c,d   Pecheyran C ^d   Keith, P ^b  

^a UNIVERSITY OF TOKYO   (Japan)

^b MUSÉUM NATIONAL D'HISTOIRE NATURELLE   (France)

^c UNIVERSITÉ DE PAU ET DES PAYS DE L'ADOUR   (France)

^d NATIONAL INSTITUTE OF STANDARDS AND TECHNOLOGY   (United States)

Author keywords

Amphidromy; Migratory behaviour; New Caledonia; Otolith microchemistry; Vanuatu

Indexed keywords

CALLOGOBIUS ATRATUS; GOBIOIDEI; PISCES; SICYOPTERUS; TELEOSTEI;

BARIUM; CALCIUM; FRESH WATER; STRONTIUM;

ANIMAL; ARTICLE; ATOMIC ABSORPTION SPECTROMETRY; CHEMISTRY; ECOSYSTEM; LOW LEVEL LASER THERAPY; PERCIFORMES; PHYSIOLOGY; VESTIBULE;

ANIMALS; BARIUM; CALCIUM; ECOSYSTEM; FRESH WATER; LASER THERAPY; OTOLITHIC MEMBRANE; PERCIFORMES; SPECTROPHOTOMETRY, ATOMIC; STRONTIUM;

EID: 84855723147     PISSN: 00221112     EISSN: 10958649     Source Type: Journal    
DOI: 10.1111/j.1095-8649.2011.03112.x     Document Type: Article

References (85)

1. Arai, T. (2006). Comparison of habitat use during early life stage between ayu Plecoglossus altivelis and ice goby Leucopsarion petresi along Sanriku Coast of Japan, as determined from otolith microchemistry. Fisheries Science 72, 382-387.
2. Arai, T. & Hirata, T. (2006). Differences in the trace element deposition in otoliths between marine- and freshwater-resident Japanese eels, Anguilla japonica, as determined by laser ablation ICPMS. Environmental Biology of Fishes 75, 173-182.
3. Arai, T., Otake, T. & Tsukamoto, K. (1997). Drastic changes in otolith microstructure and microchemistry accompanying the onset of metamorphosis in the Japanese eel, Anguilla japonica. Marine Ecology Progress Series 161, 17-22.
4. Arai, T., Otake, T. & Tsukamoto, K. (2000). Timing of metamorphosis and larval segregation of the Atlantic eels Anguilla rostrata and A. anguilla, as revealed by otolith microstructure and microchemistry. Marine Biology 137, 39-45.
5. Arai, T., Kotake, A., Lokman, P. M., Miller, M. J. & Tsukamoto, K. (2004). Evidence of different habitat use by New Zealand freshwater eels Anguilla australis and A. diffenbachii, as revealed by otolith microchemistry. Marine Ecology Progress Series 266, 213-225.
6. Arai, T., Hirata, T. & Takagi, Y. (2007). Application of laser ablation ICPMS to trace the environmental history of chum salmon Oncorhynchus keta. Marine and Environmental Research 63, 55-66.
7. Bath, G. E., Thorrold, S. R., Jones, C. M., Campana, S. E., McLaren, J. W. & Lam, J. W. (2000). Strontium and barium uptake in aragonitic otoliths of marine fish. Geochimica et Cosmochimica Acta 64, 1705-1714.
8. Bell, K. N. I. & Brown, J. A. (1995). Active salinity choice and enhanced swimming endurance in 0-8 day old larvae of diadromous gobies, including Sicydium punctatum (Pisces), in Dominica West Indies. Marine Biology 121, 409-417.
9. Campana, S. E. (1999). Chemistry and composition of fish otolith: pathways, mechanism and applications. Marine Ecology Progress Series 188, 263-297.
10. Chang, M.-Y., Wang, C.-H., You, C.-F. & Tzeng, W.-N. (2006). Individual-based dispersal patterns of larval gobies in an estuary as indicated by otolith elemental fingerprints. Scientia Marina 70S2, 165-174.
11. Closs, G. P., Smith, M., Barry, B. & Markwitz, A. (2003). Non-diadromous recruitment in coastal population of common bully (Gobiomorphus cotidianus). New Zealand Journal of Marine and Freshwater 37, 301-313.
12. Crook, D. A., Macdonald, J. I., O'Connor, J. P. & Barry, B. (2006). Use of otolith chemistry to examine patterns of diadromy in the threatened Australian grayling Prototroctes maraena. Journal of Fish Biology 69, 1330-1344.
13. Daverat, F., Tomas, J., Lahaye, M., Palmer, M. & Elie, P. (2005). Tracking continental habitat shifts of eels using otolith Sr/Ca ratios: validation and application to the coastal, estuarine and riverine eels of the Gironde-Garonne-Dordogne watershed. Marine and Freshwater Research 56, 619-627.
14. De Pontual, H., Lagardère, F., Amara, R., Bohn, M. & Ogor, A. (2003). Influence of ontogenetic and environmental changes in the otolith microchemistry of juvenile sole (Solea solea). Journal of Sea Research 50, 199-210.
15. Dessert, C., Gaillardet, J., Dupre, B., Schott, J. & Pokrovsky, O. S. (2009). Fluxes of high- versus low-temperature water-rock interactions in aerial volcanic areas: example from the Kamchatka Peninsula, Russia. Geochimica Cosmochimica Acta 73, 148-169.
16. Dittman, A. H. & Quinn, T. P. (1996). Homing in Pacific salmon: mechanisms and ecological basis. Journal of Experimental Biology 199, 83-91.
17. Elfman, M., Limburg, K. E., Kristiansson, P., Svedäng, H., Westin, L., Wickström, H., Malmqvist, K. & Pallon, J. (2000). Complex life histories of fishes revealed through natural information storage devices: case studies of diadromous events as recorded by otoliths. Nuclear Instruments and Methods in Physics Research: Beam Interactions with Materials and Atoms B 161-163, 877-881.
18. Elsdon, T. S. & Gillanders, B. M. (2004). Fish otolith chemistry influenced by exposure to multiple environmental variables. Journal of Experimental Marine Biology and Ecology 313, 269-284.
19. Elsdon, T. S. & Gillanders, B. M. (2005). Alternative life-history patterns of estuarine fish: barium in otoliths elucidates freshwater residency. Canadian Journal of Fisheries and Aquatic Sciences 62, 1143-1152.
20. Elsdon, T. S. & Gillanders, B. M. (2006). Temporal variability in strontium, calcium, barium and manganese in estuaries: implications for reconstructing environmental histories of fish from chemicals in calcified structures. Estuarine, Coastal and Shelf Science 66, 147-156.
21. Fitzsimons, J. M. & Nishimoto, R. T. (1990). Territories and site tenacity in males of the Hawaiian stream goby Lentipes concolor (Pisces: Gobiidae). Ichthyological Exploration of Freshwaters 1, 185-189.
22. Gillanders, B. M. (2005). Otolith chemistry to determine movements of diadromous and freshwater fish. Aquatic Living Resources 18, 291-300.
23. Halden, N. M., Mejia, S. R., Babaluk, J. A., Reist, J. D., Kristofferson, A. H., Campbell, J. L. & Teesdale, W. J. (2000). Oscillatory zinc distribution in Arctic char (Salvelinus alpinus) otoliths: the result of biology or environment? Fisheries Research 46, 289-298.
24. Hamer, P. A., Jenkins, G. P. & Coutin, P. (2006). Barium variation in Pagrus auratus (Sparidae) otoliths: a potential indicator of migration between an embayment and ocean waters in south-eastern Australia. Estuarine, Coastal and Shelf Science 68, 686-702.
25. Howland, K. L., Tonn, W. M., Babaluk, J. A. & Tallman, R. F. (2001). Identification of freshwater and anadromous inconnu in the Mackenzie River system by analysis of otolith strontium. Transactions of the American Fisheries Society 130, 725-741.
26. Iguchi, K. & Mizuno, N. (1991). Mechanisms of embryonic drift in the amphidromous goby Rhinogobius brunneus. Environmental Biology of Fishes 31, 295-300.
27. Jackson, D. A., Peres-Neto, P. R. & Olden, J. D. (2001). What controls who is where in freshwater fish communities - the roles of biotic, abiotic, and spatial factors. Canadian Journal of Fisheries and Aquatic Sciences 58, 157-170.
28. Jessop, B. M., Shiao, J.-C., Iizuka, Y. & Tzeng, W.-N. (2002). Migratory behaviour and habitat use by American eels Anguilla rostrata as revealed by otolith microchemistry. Marine Ecology Progress Series 233, 217-229.
29. Jessop, B. M., Shiao, J.-C., Iizuka, Y. & Tzeng, W.-N. (2006). Migration of juvenile American eels Anguilla rostrata between freshwater and estuary as revealed by otolith microchemistry. Marine Ecology Progress Series 310, 219-233.
30. Kabata-Pendias, A. & Pendias, H. (2001). Trace Elements in Soils and Plants, 3rd edn. Boca Raton, FL: CRC Press.
31. Kalish, J. M. (1990). Use of otolith microchemistry to distinguish the progeny of sympatric anadromous and non-anadromous salmonids. Fishery Bulletin 88, 657-666.
32. Keith, P. (2003). Biology and ecology of amphidromous Gobiidae in the Indo-Pacific and the Caribbean regions. Journal of Fish Biology 63, 831-847.
33. Keith, P. & Lord, C. (2011). Tropical freshwater gobies: amphidromy as a life cycle. In The Biology of Gobies (Patzner, R. A., Van Tassell, J. L., Kovacic, M. & Kapoor, B. G., eds), pp. 243-277. New York, NY: Science Publishers Inc.
34. Keith, P., Watson, R. E. & Marquet, G. (2004). Sicyopterus aiensis, a new species of freshwater goby from Vanuatu (Teleostei: Gobioidei). Cybium 28, 111-118.
35. Keith, P., Lord, C. & Vigneux, E. (2006). In vivo observations on post-larval development of freshwater gobies and eleotrids from French Polynesia and New Caledonia. Ichthyological Exploration of Freswaters 17, 187-191.
36. Keith, P., Hoareau, T. B., Lord, C., Ah-Yane, O., Gimmoneau, G., Robinet, T. & Valade, P. (2008). Characterisation of post-larval to juvenile stages, metamorphosis and recruitments of an amphidromous goby, Sicyopterus lagocephalus (Pallas) (Teleostei: Gobiidae: Sicydiinae). Marine and Freshwater Research 59, 876-889.
37. Keith, P., Lord, C., Marquet, G. & Kalfatak, D. (2009). Biodiversity and biogeography of amphidromous fishes from New Caledonia, a comparison with Vanuatu. Zoologia Neocaledonica 7. Biodiversity Studies in New Caledonia. Mémoires du Muséum national d'Histoire naturelle 198, 175-183.
38. Keith, P., Lord, C., Gerbeaux, P. & Kalfatak, D. (2011). Freshwater biota. Focus on fish, shrimps and crabs. In Natural History of Santo (Bouchet, P., Le Guyader, H. & Pascal, O., eds), pp. 242-251. Paris: Publications Scientifiques du MNHN.
39. Kido, M. H. & Heacock, D. E. (1992). The spawning ecology of o'opu-nakea (Awaous stamineus) in Wainiha River. In New Directions in Research Management and Conservation of Hawaiian Freshwater Stream, Biology and Fisheries Management (Devick, W., ed.), pp. 142-157. Honolulu, HI: Department of Aquatic Resources.
40. Kraus, R. T. & Secor, D. H. (2004). Incorporation of strontium into otoliths of an estuarine fish. Journal of Experimental Marine Biology and Ecology 302, 85-106.
41. Kuroki, M., Tao, M., Ishida, R. & Tsukamoto, K. (2006). Migratory history of wild and released ayu (Plecoglossus altivelis) in the Korube River, Japan. Coastal and Marine Science 30, 425-431.
42. Lecomte-Finiger, R. (1999). L'otolithe: la "boîte noire" des Téléostéens. Année Biologique 38, 107-122.
43. 226Ra from river-borne sediments in the Hudson estuary. Earth and Planetary Science Letters 43, 343-350.
44. Limburg, K. E. (1995). Otolith strontium traces environmental history of subyearling American shad Alosa sapidissima. Marine Ecology Progress Series 119, 25-36.
45. Lindstrom, D. P. (1998). Reproduction, early development and larval transport dynamics of amphidromous Hawaiian Gobioids. PhD Thesis, University of Michigan, Ann Arbor, MI, U.S.A.
46. Ling, Y. J., Iizuka, Y. & Tzeng, W. N. (2005). Decreased Sr/Ca ratios in the otoliths of two marine eels, Gymnothorax reticularis and Muraenesox cinereus, during metamorphosis. Marine Ecology Progress Series 304, 201-206.
47. Lord, C. & Keith, P. (2008). Threatened fishes of the world: Sicyopterus sarasini Weber & Beaufort, 1915 (Gobiidae). Environmental Biology of Fishes 83, 169-170.
48. Lord, C., Brun, C., Hautecoeur, M. & Keith, P. (2010). Insights on endemism: comparison of the duration of the marine larval phase estimated by otolith microstructural analysis of three amphidromous Sicyopterus species (Gobioidei: Sicydiinae) from Vanuatu and New Caledonia. Ecology of Freshwater Fish 19, 26-38.
49. Louvat, P. & Allègre, C. J. (1997). Present denudation rates on the island of Réunion determined by river geochemistry: basalt weathering and mass budget between chemical and mechanical erosions. Geochimica Cosmochimica Acta 61, 3645-3669.
50. Louvat, P. & Allègre, C. J. (1998). Riverine erosion rates on Sao Miguel volcanic island, Azores archipelago. Chemical Geology 148, 177-200.
51. Marquet, G., Keith, P. & Vigneux, E. (2003). Atlas des poissons et des crustacés d'eau douce de Nouvelle-Calédonie Patrimoines Naturels 58.
52. McCulloch, M., Fallon, S., Wyndham, T., Hendy, E., Lough, J. & Barnes, D. (2003). Coral record of increased sediment flux to the inner Great Barrier Reef since European settlement. Nature 421, 727-730.
53. McCulloch, M., Cappo, M., Aumend, J. & Müller, W. (2005). Tracing the life history of individual barramundi using laser ablation MC-ICP-MC Sr-isotopic and Sr/Ba ratios in otoliths. Marine and Freshwater Research 56, 637-644.
54. Milton, D. A. & Chenery, S. R. (2001). Sources and uptake of trace metals in otoliths of juvenile barramundi (Lates calcarifer). Journal of Experimental Marine Biology and Ecology 264, 47-65.
55. Milton, D., Halliday, I., Sellin, M., Marsh, R., Staunton-Smith, J. & Woodhead, J. (2008). The effect of habitat and environmental history on otolith chemistry of barramundi Lates calcarifer in estuarine populations of a regulated tropical river. Estuarine, Coastal and Shelf Science 78, 301-315.
56. Monti, D. & Legendre, P. (2009). Shifts between biotic and physical driving forces of species organization under natural disturbance regimes. Canadian Journal of Fisheries and Aquatic Sciences 66, 1282-1293.
57. Myers, G. S. (1949). Usage of anadromous, catadromous and allied terms for migratory fishes. Copeia 1949, 49-97.
58. Nishimoto, R. T. & Fitzsimons, J. M. (1986). Courtship, territoriality, and coloration in the endemic Hawaiian freshwater goby, Lentipes concolor. In Indo-Pacific Fish Biology, Proceedings of the 2nd International Conference on Indo-Pacific Fishes, Tokyo (Uyeno, T., Arai, R., Taniuchi, T. & Matsuura, K., eds), pp. 811-817. Tokyo: Ichthyological Society of Japan.
59. Otake, T. & Uchida, K. (1998). Application of otolith microchemistry for distinguishing between amphidromous and non-amphidromous stocked ayu, Plecoglossus altivelis. Fisheries Science 64, 517-521.
60. Pannella, G. (1971). Fish otoliths: daily growth layers and periodical patterns. Science 173, 1124-1127.
61. Pfeifer, H.-R., Derron, M.-H., Rey, D., Schlegel, C., Atteia, O., Dalla Piazza, R., Dubois, J.-P. & Mandia, Y. (2000). Natural trace element input to the soil-sediment- water plant system: examples of background and contaminated situations in Switzerland, Eastern France and Northern Italy. In Trace Elements - Their Distribution and Effects in the Environment (Markett, B. & Friese, K., eds), pp. 33-86. Amsterdam: Elsevier.
62. Rad, S. D., Allègre, C. J. & Louvat, P. (2007). Hidden erosion on volcanic islands. Earth and Planetary Science Letters 262, 109-124.
63. Radtke, R. L. (1989). Strontium-calcium concentration ratios in fish otoliths as environmental indicators. Biochemistry and Physiology Part A 92, 189-193.
64. Radtke, R. L. & Kinzie, R. A. III (1996). Evidence of a marine larval stage in endemic Hawaiian stream gobies from isolated high-elevation locations. Transactions of the American Fisheries Society 125, 613-621.
65. Radtke, R. L., Townsend, D. W., Kinzie, R. A. III & Fey, D. (1999). Two-dimensional X-ray mapping of otoliths, a high-resolution technique for determining amphidromy in the tropical goby Lentipes concolor (Gill). Journal of Experimental Marine Biology and Ecology 238, 21-27.
66. Secor, D. H. & Rooker, J. R. (2000). Is otolith strontium a useful scalar of life cycles in estuarine fishes? Fisheries Research 46, 359-371.
67. Secor, D. H., Henderson-Arzapalo, A. & Piccoli, P. M. (1995). Can otolith microchemistry chart patterns of migration and habitat utilization in anadromous fishes? Journal of Experimental Marine Biology and Ecology 192, 15-33.
68. Shen, K. N. & Tzeng, W. N. (2002). Formation of a metamorphosis check in otoliths of the amphidromous goby Sicyopterus japonicus. Marine Ecology Progress Series 228, 205-211.
69. Shen, K. N., Lee, Y. C. & Tzeng, W. N. (1998). Use of otolith microchemistry to investigate the life history pattern of gobies in a Taiwanese stream. Zoological Studies 37, 322-329.
70. Shiao, J. C., Lozys, L., Iizuka, Y. & Tzeng, W. N. (2006). Migratory patterns and contribution of stocking to the population of European eel in Lithuanian waters as indicated by otolith Sr:Ca ratios. Journal of Fish Biology 69, 749-769.
71. Tabouret, H., Bareille, G., Claverie, F., Pécheyran, C., Prouzet, P. & Donard, O. F. X. (2010). Simultaneous use of strontium:calcium and barium:calcium ratios in otoliths as markers of habitat: application to the European eel (Anguilla anguilla) in the Adour basin, South West France. Marine Environmental Research 70, 35-45.
72. Taillebois, L., Keith, P., Valade, P., Torres, P., Baloche, S. & Dufour, S. (2011). Involvement of thyroid hormones in the control of larval metamorphosis in Sicyopterus lagocephalus (Teleostei: Gobioidei) at the time of river recruitment. General and Comparative Endocrinology. 173, 281-288. DOI: 10.1016/j.ygcen.2011.06.008
73. Tamada, K. (2001). Clutch size and egg size in three species of Rhinogobius complex dwelling in a single stream. Japanese Journal of Ichthyology 48, 49-52.
74. Tsukamoto, K. & Arai, T. (2001). Facultative catadromy of the eel Anguilla japonica between freshwater and seawater habitats. Marine Ecology Progress Series 220, 265-276.
75. Tsukamoto, K., Nakai, I. & Tesch, W.-V. (1998). Do all freshwater eels migrate? Nature 396, 635-636.
76. Tsunagawa, T. & Arai, T. (2008). Flexible migration of Japanese freshwater gobies Rhinogobius spp. as revealed by Sr:Ca ratios. Journal of Fish Biology 73, 2421-2433.
77. Tsunagawa, T., Suzuki, T. & Arai, T. (2009). Migratory history of Rhinogobius sp. OR morphotype "Shimahire" as revealed by otolith Sr:Ca ratios. Ichthyological Research 57, 10-15.
78. Turner, D. R., Whitfield, M. & Dickson, A. G. (1981). The equilibrium speciation of dissolved components in freshwater and seawater at 25°C and 1 atm pressure. Geochimica and Cosmochimica Acta 45, 855-881.
79. Tzeng, W. N. (1996). Effects of salinity and ontogenetic movements on strontium:calcium ratios in the otoliths of Japanese eel, Anguilla japonica Temminck and Schlegel. Journal of Experimental Marine Biology and Ecology 199, 111-122.
80. Valade, P., Lord, C., Grondin, H., Bosc, P., Taillebois, L., Iida, M., Tsukamoto, K. & Keith, P. (2010). Early life history and description of larval stages of an amphidromous goby, Sicyopterus lagocephalus (Gobioidei: Sicydiinae). Cybium 33, 309-319.
81. de Vries, M. C., Gillanders, B. M. & Elsdon, T. S. (2005). Facilitation of barium uptake into fish otoliths: influence of strontium concentration and salinity. Geochimica et Cosmochimica Acta 69, 4061-4072.
82. Watson, R. E., Keith, P. & Marquet, G. (2007). Akihito vanuatu, a new genus and new species of freshwater goby from the South Pacific (Teleostei: Gobioidei: Sicydiinae). Cybium 31, 341-349.
83. Wells, B. K., Rieman, B. E., Clayton, J. L., Horan, D. L. & Jones, C. M. (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. Transactions of the American Fisheries Society 132, 409-424.
84. Yokoi, K. & Hosoya, K. (2005). Larval salinity tolerance in the endangered goby Rhinogobius sp. BI (Gobiidae) from the Bonin Islands. Japanese Journal of Ichthyology 52, 31-34.
85. Yuma, M., Maruyama, A. & Rusuwa, B. (2000). Behaviour and distribution of upstream-migrating juvenile Rhinogobius sp. (the orange form). Ichthyological Research 47, 379-384.