[BPT06-P07] Radio- and stable carbon isotopic responses in experimentally-cultured bivalves for the understanding of acidification effect on bivalve nutrient uptake and biomineralization
Keywords:Mollusca, Radio isotope, Stable carbon isotope
The effects of ocean acidification on bivalve growth and calcification have been widely debated in recent years due to potential impacts on the aquaculture sector and thus marine biodiversity. This study aims to elucidate the effects of ocean acidification on bivalve nutrient assimilation into its various components via laboratory culture experiments at six different pCO2 levels at 25 °C (332, 463, 653, 872, 1137, and 1337 μatm). Radio carbon (Δ14C) and stable carbon (δ13C) isotopic analysis will be undertaken to investigate: (1) the proportion of incorporation of carbon from ambient DIC and metabolic CO2 into bivalve shell and tissues; and (2) effects of changing pCO2 concentrations on carbon incorporation. Our research marks the first attempt to trace partitioning of nutrients within a single species via application of bomb-pulse radiocarbon principles. By using modern samples in a culture experiment of ocean acidification by using CO2 gas derived from fossil fuels, differences in contribution from end-members of DIC and metabolic CO2 can be clearly resolved in high resolution. Combination of radiocarbon techniques with stable isotopic analysis will allow biological contributions to be parsed from a geochemical perspective, providing a comprehensive understanding of bivalve nutrient assimilation.
Specimens of the filter-feeding clam Scapharca broughtonii (Bivalvia: Arcidae) were cultured in aquaria for 8 weeks, with a novel high-precision pCO2 control system which maintained steady CO2 levels. Bivalve shells and soft tissues, as well as the relevant water and plankton feed samples, were then analysed for δ13C in an Isotope Ratio Mass Spectrometer (IRMS) and Δ14C in an Accelerator Mass Spectrometer (AMS) to examine variations in end-member contributions to the bivalve components.
Shell carbon was found to be principally derived from seawater DIC in all pCO2 conditions. Mantle and soft tissue isotopic signatures stayed constant across pCO2 concentrations and were primarily correlated with the organic carbon signal. A high degree of correlation between Δ14C values of bivalve shell and seawater DIC may point to S. broughtonii’s suitability as a geochemical proxy of DIC palaeo-concentrations. Using Δ14C in concert with δ13C allowed separation of isotopic fractionations deriving from effects other than those caused by actual changes in end-member contributions. Shell δ13C thus might indicate biologically-related fractionation due to physiological adaptations to cope with effects of changes in ambient pH as these dictated the magnitude of this species-specific effect.
Specimens of the filter-feeding clam Scapharca broughtonii (Bivalvia: Arcidae) were cultured in aquaria for 8 weeks, with a novel high-precision pCO2 control system which maintained steady CO2 levels. Bivalve shells and soft tissues, as well as the relevant water and plankton feed samples, were then analysed for δ13C in an Isotope Ratio Mass Spectrometer (IRMS) and Δ14C in an Accelerator Mass Spectrometer (AMS) to examine variations in end-member contributions to the bivalve components.
Shell carbon was found to be principally derived from seawater DIC in all pCO2 conditions. Mantle and soft tissue isotopic signatures stayed constant across pCO2 concentrations and were primarily correlated with the organic carbon signal. A high degree of correlation between Δ14C values of bivalve shell and seawater DIC may point to S. broughtonii’s suitability as a geochemical proxy of DIC palaeo-concentrations. Using Δ14C in concert with δ13C allowed separation of isotopic fractionations deriving from effects other than those caused by actual changes in end-member contributions. Shell δ13C thus might indicate biologically-related fractionation due to physiological adaptations to cope with effects of changes in ambient pH as these dictated the magnitude of this species-specific effect.