Sustained alpha oscillations serve attentional prioritization in working memory, not maintenance.

Recent theory on the neural basis of working memory (WM) has attributed an important role to "activity-silent" or -quiescent mechanisms, suggesting that sustained neural activity might not be essential in the retention of information. This idea has been challenged by reports of ongoing neural activity in the alpha band during WM maintenance, however. The precise role of these alpha oscillations is unclear: Do they reflect attentional prioritization of stored information, or do they serve as a general maintenance mechanism, for instance to periodically refresh synaptic traces? To address this, we designed a visual WM task involving two memory items, one of which was prioritized by being tested first for recall. The task included both short (1 second) and long (3 seconds) delay intervals between encoding and retrieval. The long delay condition allowed us to test whether the alpha-based decoding effects persist beyond the early delay period, thereby putting accounts that attribute alpha activity to generic maintenance processes to the test. Time-resolved decoding analyses revealed that both tested-first and tested-second items were initially decodable following stimulus presentation. However, only the tested-first item exhibited sustained decodability throughout the delay, particularly in the long delay condition, where it transitioned into a stable coding scheme. This prolonged representation was selectively supported by induced alpha power, which reliably tracked the prioritized tested-first item, but not the deprioritized tested-second item. Impulse-based decoding further confirmed this asymmetry, showing a selective increase in readout for the tested-second item only when it became immediately task relevant. Together, these findings suggest that sustained alpha-band activity primarily reflects attentional prioritization, rather than general memory maintenance. Unattended, deprioritized items appear to transition into an activity-quiescent state, consistent with models of synaptic storage in WM.