Published December 7, 2021
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Integrative Assessment of Sediments Affected by CO2 Enrichment: A Case Study in the Bay of Santos—SP, Brazil

  • 1. Department of Environment, Petrobras, Santos 11010-310, Brazil
  • 2. Department of Physico-Chemistry, Aquatic Systems Research Group, UNESCO/UNITWIN WiCop, Faculty of Environmental and Marine Sciences, 11510 Cádiz, Spain
  • 3. Centro de Investigaciones Costeras—Universidad de Atacama (CIC-UDA), University of Atacama, Copiapó 1530000, Chile
  • 4. Department of Ocean Sciences, Federal University of São Paulo (UNIFESP), Santos 11030-100, Brazil
  • 5. Federal University of São Paulo
  • 6. Department of Ecotoxicology, Santa Cecília University (UNISANTA), Boqueirão 11045-907, Brazil

Description

CO2 enrichment in the marine environment caused by leakages from carbon capture and storage technologies may occur over operational procedures. An integrated approach using weight-of-evidence was applied to assess the environmental risk associated with the acidification caused by CO2 enrichment in coastal sediments from Santos (Brazil). Chemical analyses (metal(loid)s and organic contaminant (e.g., hydrocarbons), toxicity tests (amphipods mortality, sea-urchin embryo-larval development) and macro-benthic community structure alteration assessment were performed with different acidified scenarios (pH 8.0–6.0) for two stations with different contamination degrees. These lines of evidence were statistically analyzed and integrated (multivariate analysis and ANOVA). Results of toxicity showed significant chronic effects starting at pH 7.0 while acute effects were observed starting at pH 6.5. The macro-benthic community integrity showed significant differences for all treatments at the Piaçaguera channel station, considered to be moderately contaminated. Results from the multivariate analysis correlated toxic effects and increase in the mobility of some elements with acidification. Also, the biological indexes were correlated with concentrations of dissolved Zn in seawater. The pH of 6.0 was extremely toxic for marine life due to its high acidification and metal bioavailability. The approach herein identified and discriminated the origin of the degradation caused by the acidification related to the enrichment of CO2.
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