4.7 Article

Calcium and strontium isotope systematics in the lagoon-estuarine environments of South Australia: Implications for water source mixing, carbonate fluxes and fish migration

Journal

GEOCHIMICA ET COSMOCHIMICA ACTA
Volume 239, Issue -, Pages 90-108

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2018.07.036

Keywords

Calcium; Strontium; Isotopes; Water mixing; Carbonate fluxes; Otoliths; PHREEQC

Funding

  1. Czech Science Foundation (GACR grant) [17-18120S]
  2. Environment Institute
  3. University of Adelaide
  4. Australian Research Council [DP110100716, FT100100767]
  5. Base-Line Earth project - European Commission via the Marie Currie (ITN MC) grant under Horizon 2020 program [643084]
  6. ARC Linkage project (ARC grant) [LP160101353]
  7. Fundacao para a Ciencia e Tecnologia [UID/MAR/04292/2013, SFRH/BPD/95784/2013]
  8. Adelaide Graduate Research Scholarship
  9. CRC Landscape Environments and Mineral Exploration (LEME) Regolith Science Supplementary Scholarship
  10. Australian Research Council [LP160101353] Funding Source: Australian Research Council
  11. Fundação para a Ciência e a Tecnologia [SFRH/BPD/95784/2013] Funding Source: FCT
  12. Marie Curie Actions (MSCA) [643084] Funding Source: Marie Curie Actions (MSCA)

Ask authors/readers for more resources

This study uses Ca and Sr isotopes (delta Ca-44/40 and Sr-87/Sr-86), coupled with elemental ratios, to better understand the water source apportionment and carbonate output in the Coorong, Lower Lakes and Murray Mouth Estuary, which represents the terminus of Australia's longest river system. The geochemistry of waters in the Coorong (i.e., North and South Lagoon) can be explained by mixing of three major components, including: (i) the Southern Ocean seawater, (ii) local freshwaters, and (iii) hypersaline lagoon waters, the latter significantly modified by ongoing evaporation and carbonate formation. The Sr and Ca isotope composition of the North Lagoon is indistinguishable from that of the Southern Ocean (i.e., normal salinity of similar to 35 PSU), with the exception of transient freshwater input events that can temporarily lower the salinity to brackish levels. Interestingly, our results from the hypersaline South Lagoon (salinity up to similar to 120 PSU) confirmed that the latter is highly evaporated brackish water (with >= 40% contribution from continent-derived waters), which has been additionally modified by in-situ carbonate precipitation. Importantly, our Ca isotope and elemental constraints showed that about 15-17% of the dissolved Ca2+ in the South Lagoon has been removed as CaCO3 (primarily as aragonite). This in turn has implications for the local carbonate cycle and blue carbon studies, suggesting that the South Lagoon acts as a net sink for the dissolved inorganic carbon (DIC). Ca isotope data from the otoliths of smallmouth hardyhead fish species (Atherinosoma microstoma) collected in the Coorong indicate that delta(44)/Ca-40 is primarily controlled by biological processes (i.e., kinetic isotope fractionation effects related to growth rate), rather than by the Ca isotope composition of local lagoon waters. As to Sr-87/Sr-86 in otoliths, the latter confirmed the importance of continent-derived water sources in the Coorong, recorded over the life span of the fish. Overall, with suitable fossil carbonate archives (e.g., bivalve shells, foraminifera), our calibration of Sr-87/Sr-86 and delta(44)/Ca-40 in the modern hydrological system, with respect to a large salinity gradient (ranging from fresh to hypersaline, i.e., 0 to similar to 120 PSU), implies potential future applications of these isotope tracers in carbonate-producing coastal systems, which include (i) tracing and apportioning different water sources, (ii) quantifying local carbonate outputs, and (iii) reconstructing paleosalinity changes. (C) 2018 Elsevier Ltd. All rights reserved.

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