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Dynamic oxygen landscapes modulate eco-physiological responses to mercury exposure in the bivalve Ruditapes philippinarum

TitleDynamic oxygen landscapes modulate eco-physiological responses to mercury exposure in the bivalve Ruditapes philippinarum
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2026
AuthorsD'Aniello, Ilaria, Fabrello Jacopo, Campaci Chiara Margherita, Capasso Annalisa, Ciampaglia Roberto, Manzo Sonia, Moro Isabella, Pavanello Sabrina, Simonelli Martina, Roviezzo Fiorentina, Matozzo Valerio, and Munari Marco
JournalMarine Pollution Bulletin
Volume232
Type of ArticleArticle
ISSN0025326X
Keywordsacetylcholinesterase, adult, animal experiment, Antioxidant, article, Atomic absorption spectrometry, bioaccumulation, biochemical analysis, Biochemical oxygen demand, biogenic oxygen production, biological marker, bivalve, blood cell, blood cell count, Catalase, chemical pollution, clam, clam culture, Coastal ecosystems, controlled study, dissolved oxygen, dynamic oxygen landscapes, ecophysiology, Ecosystems, enzyme activity, exocrine gland, exposure, gill, glutathione, Glutathione Transferase, heavy metal, Hemocyte, hemolymph, Hyperoxia, Impurities, lipid peroxidase, lipid peroxidation assay, mercuric chloride, mercury, mercury (element), Mercury (metal), Mercury compounds, Mercury exposure, microwave assisted extraction, Molluscs, Multiple driver' exposure, multiple drivers exposure, nonhuman, Oxidative stress, Oxygen, Oxygen regime, oxygen saturation, oxygen supersaturation, Oxyscape, oxyscapes, photosynthesis, Physiological models, physiological response, physiological stress, Pollution, Primary producers, Protein, Risk assessment, Ruditapes philippinarum, Salinity, Shellfish, software, spatiotemporal analysis, spectrophotometry, superoxide dismutase, Supersaturation, thiobarbituric acid reactive substance, thiobarbituric acid reactive substances assay, total hemocyte count, xanthine oxidase method
Abstract

Coastal ecosystems are characterized by strong diel fluctuations in dissolved oxygen driven by primary producers, generating dynamic ‘oxyscapes’ that can modulate organism physiology. While oxygen supersaturation can buffer climate-related stressors, its role in mediating contaminant effects remains poorly understood. We investigated whether oxygen supersaturation influences physiological impact of mercury (HgCl₂) in the clam Ruditapes philippinarum. Clams were exposed for 7 days to a fully factorial combination of two oxygen regimes (normoxia: 90% saturation; diel hyperoxia: >150% for 5 h day−1) and two Hg concentrations (0 and 1 μg L−1). Haemocyte traits (count, diameter, volume) and a battery of biomarkers were measured in gills and digestive gland. Bioaccumulation of mercury was also investigated. Hyperoxia did not buffer mercury toxicity but modulated organism responses across multiple biological levels. Mercury and hyperoxia reduced haemocyte size, but not cell abundance. Mercury increased lipid peroxidation, while antioxidant responses were tissue-specific and inconsistently regulated. Hyperoxia independently increased oxidative stress, whereas combined mercury and hyperoxia exposure affected gill CAT activity. Oxygen regime influenced baseline mercury levels but did not reduce bioaccumulation under exposure conditions. These findings demonstrated that oxygen supersaturation reshapes rather than mitigates contaminant effects, highlighting a decoupling between metabolic support and physiological stress. Within dynamic oxyscapes, oxygen availability emerges as a key driver of both exposure and response pathways, with implications for organism vulnerability under multi-stressor scenarios. Our results challenge the assumption that biogenic oxygen production can buffer chemical pollution and emphasise the need to integrate oxygen dynamics into ecophysiological and risk assessment frameworks. © 2026 The Authors.

Notes

Cited by: 0; All Open Access; Green Open Access; Hybrid Gold Open Access

URLhttps://www.scopus.com/pages/publications/105042602762?origin=resultslist
DOI10.1016/j.marpolbul.2026.120056
Citation KeyD'Aniello2026
PubMed ID42341450