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This paper introduces REACT, a novel machine learning framework designed to reconstruct global sea surface pH while strictly enforcing physical and chemical conservation laws. By decoupling transport dynamics from active chemical corrections, the model addresses a critical limitation in existing AI approaches that often violate carbonate closure when handling active tracers like pH. The method demonstrates significant improvements in prediction accuracy and consistency over standard baselines, offering a robust tool for monitoring ocean acidification without relying on computationally expensive traditional inverse models.
REACT: Physically and Chemically Consistent Reconstruction of Marine Active Tracers
arXiv:2610.03888v1 Announce Type: new Abstract: Reconstructing global sea surface pH from sparse observations is critical for monitoring ocean acidification and understanding marine carbon cycling. Traditional assimilation and inverse models are physically grounded but costly for large-scale reconstruction. Recent black-box and physics-guided AI models improve efficiency, but are mainly designed for passive tracers, where the reconstructed variable is also the transported inventory. In contrast, pH is an active carbonate tracer: it is the prediction target, while dissolved inorganic carbon (DIC) is the conserved carbon inventory. This mismatch can produce low pH error while violating carbonate closure and source-free carbon conservation. To address this, we introduce \textbf{REACT}, a carbon-first reconstruction framework that decouples transport, active correction, and chemical decoding. REACT transports a latent carbonate state with a conservative advection--diffusion solver, captures non-conservative carbon-cycle variations with a source module, decodes the corrected state into pH, and constrains the output through carbonate equilibrium. This design keeps pH as the target while enforcing consistency on the underlying carbon state. On simulation data, REACT reduces pH NRMSE by (14.7%) and chemical consistency error by (24.0%) over the best baseline. Cross-temporal-scale evaluations show robustness against error accumulation from coarse to fine temporal scales, and ablation studies validate the effectiveness of each component.
Abstract:Reconstructing global sea surface pH from sparse observations is critical for monitoring ocean acidification and understanding marine carbon cycling. Traditional assimilation and inverse models are physically grounded but costly for large-scale reconstruction. Recent black-box and physics-guided AI models improve efficiency, but are mainly designed for passive tracers, where the reconstructed variable is also the transported inventory. In contrast, pH is an active carbonate tracer: it is the prediction target, while dissolved inorganic carbon (DIC) is the conserved carbon inventory. This mismatch can produce low pH error while violating carbonate closure and source-free carbon conservation. To address this, we introduce \textbf{REACT}, a carbon-first reconstruction framework that decouples transport, active correction, and chemical decoding. REACT transports a latent carbonate state with a conservative advection--diffusion solver, captures non-conservative carbon-cycle variations with a source module, decodes the corrected state into pH, and constrains the output through carbonate equilibrium. This design keeps pH as the target while enforcing consistency on the underlying carbon state. On simulation data, REACT reduces pH NRMSE by (14.7%) and chemical consistency error by (24.0%) over the best baseline. Cross-temporal-scale evaluations show robustness against error accumulation from coarse to fine temporal scales, and ablation studies validate the effectiveness of each component.
Artificial Intelligence (cs.AI); Machine Learning (cs.LG)
arXiv:2610.03888 [cs.AI]
(or arXiv:2610.03888v1 [cs.AI] for this version)
https://doi.org/10.48550/arXiv.2610.03888 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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