Diaz, A.; Tal, I.; Markowitz, N.; Grossman, S.; Espinal, E.; Tostaeva, G.; schroeder, c.; Mehta, A.; Neymotin, S.; Bickel, S.

Transient high-frequency activity (HFA) in local field potentials exhibits substantial variability across trials and behavioral states, yet its functional role in sensory representation remains poorly understood. Here, we tested whether transient HFA events carry stimulus-related information through their temporal, spectral, and phase-dependent properties. Using intracranial recordings from 21 human participants performing a visual localizer task, we extracted transient HFA events and quantified their features using information-theoretic and decoding analyses. Individual event features carried only modest information about stimulus identity, and response magnitude and morphology-related properties contributed minimally to decoding performance. Instead, decoding was dominated by temporal alignment and low-frequency phase. Critically, representing transient events as distributed low-frequency phase configurations across electrodes substantially improved cross-trial decoding performance, whereas disrupting distributed phase structure eliminated this decoding advantage. These findings indicate that stimulus-related structure in transient HFA does not primarily arise from isolated local event properties, but instead emerges through distributed, phase-dependent network dynamics. More broadly, the results provide a framework for understanding how transient high-frequency neural activity contributes to sensory representations across distributed cortical networks.