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Bred oysters switch shell carbon under acidification

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Selectively bred Saccostrea glomerata keep more ordered calcite and can use different DIC pathways than wild-type oysters in acidified Australian estuaries.

Source

Selectively bred oysters can alter their biomineralization pathways, promoting resilience to environmental acidification

Fitzer SC, McGill RAR, Torres Gabarda S, et al. · Global change biology · 2019

doi.org/10.1111/gcb.14818Read the full paper ↗24 citationscc by

What they did

Families bred for QX resistance or fast growth plus wild-type oysters were sampled from control (~pH 8.1–8.2) and acidified (~pH 7.4–7.5) leases; shells were mapped by EBSD and δ13C was measured in seawater, shell, tissue, and extrapallial fluid.

What they found

Acidified seawater was isotopically lighter. Wild-type shells showed more crystallographic disorder. Under acidification shell δ13C went negative, consistent with a switch from HCO3− toward CO32− as the carbon source; selected families already used the CO32−-like signature at control sites.

The limits

What it doesn't show

Small n (12 oysters, 3 per SEM/isotope analysis) and covarying salinity, temperature, and food mean acidification is not isolated; commercial breeding is not a reef-restoration trial.

Key terms

Coastal acidification
Low pH in estuaries driven by land runoff and acid sulfate soils, not only atmospheric CO2.
δ13C
Carbon-isotope ratio used to infer whether shell carbon comes from HCO3− or CO32− pools.
EBSD
Electron backscatter diffraction mapping of calcite crystal orientation.
Saccostrea glomerata
Sydney rock oyster farmed in NSW estuaries.
Extrapallial fluid
Fluid between mantle and shell where calcification occurs.

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Acidified lease pH was about:

Common questions

What pH did acidified leases reach?

About pH 7.4–7.5 versus control 8.1–8.2.

Which shells were more disordered?

Wild-type (F31) calcite vs selected F15/F30.

What happens to shell δ13C under acidification?

It becomes significantly lighter (negative).

Why does that matter?

It implies a shift in inorganic carbon source used for biomineralization.

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