Adult exposure influences offspring response to ocean acidification in oysters

By L. Parker, Pauline Ross, W. O'Connor, Larissa Borysko, D. Raftos, H. Pörtner. 2012

457 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/2894b93b7903d8746c667af61623b3a3a6bfd0bb

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In Global and Planetary Change

In Oceanography

Citations in the corpus

Impacts of ocean acidification on marine shelled molluscs (2013, background): “Similar decreases in larval size and increases in abnormal development were reported for S. glomerata in a study by Watson et al. (2009) and Parker et al. (2012).”
Elevated pCO2 causes developmental delay in early larval Pacific oysters, Crassostrea gigas (2013, background): “The effects of ocean acidification have been studied on populations of C. gigas from Japan (Kurihara et al. 2007), Australia (Parker et al. 2010, 2012), and Europe (Gazeau et al. 2011), but few studies to date look at these effects on populations of C. gigas from the United States.”
A developmental and energetic basis linking larval oyster shell formation to acidification sensitivity (2013, background): “…vary strongly as a function of life-history stage and food availability [Green et al., 2009; Waldbusser et al., 2010; Melzner et al., 2011], or on previous exposure of reproductive adults and larvae to acidified waters [Barton et al., 2012; Hettinger et al., 2012; Parker et al., 2012].”
Long-term and trans-life-cycle effects of exposure to ocean acidification in the green sea urchin Strongylocentrotus droebachiensis (2013, background): “In a recent paper, Parker et al. (2012) pre-exposed adult oysters to high pCO2 (856 latm) for 5 weeks during reproductive conditioning and showed a positive carry-over effect on larval growth.”
Effects of sea-water acidification on fertilization and larval development of the oyster Crassostrea gigas (2013, background): “Some of these detrimental effects may, however, be attenuated by the capacity of the organisms to acclimate or adapt to elevated pCO2 over the next century (Parker et al., 2012), so caution is advised when extrapolating results to natural populations.”
Linking the biological impacts of ocean acidification on oysters to changes in ecosystem services: A review (2017, background): “However, Parker et al. (2015; 2012) 333 demonstrated conferred tolerance from adults exposed to elevated CO2 to their 334 offspring (also dependent on if the oysters originated from wild or aquaculture-335 reared populations), suggesting hereditary traits as a mechanism of resilience.”
Sydney Harbour: a review of anthropogenic impacts on the biodiversity and ecosystem function of one of the world’s largest natural harbours (2015, result): “Larvae spawned from adults exposed to elevated pCO2 were larger and developed faster, but displayed similar survival compared with larvae spawned from adults exposed to ambient pCO2 (Parker et al. 2012).”
Non-genetic inheritance and changing environments (2013, background): “The notion of TGP has appeared under various names, including maternal environmental effects [13], intergenerational effects [14], legacy or carry-over effects [15], cross-generational plasticity [16], and trans-generational acclimation [17].”
High-Frequency Dynamics of Ocean pH: A Multi-Ecosystem Comparison (2011, background): “Additionally, these species must also tolerate abiotic factors that interact with pH, such as temperature [62].”
Adaptation and the physiology of ocean acidification (2013, unknown): “2011), oysters (Parker et al. 2012) and coccolithophores (Langer et al.”
The physiological and molecular responses of larvae from the reef-building coral Pocillopora damicornis exposed to near-future increases in temperature and pCO2 (2012, background): “Previous work in non-brooding systems suggests positive carry-over effects in oysters (Parker et al. 2012), which could have substantial implications for future population response.”