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Sediment resuspension in coastal environments is associated with both nutrient repartitioning and with the biological carbon pump, which are further linked to climate change, eutrophication, and marine pollution. To explore these relationships, a resuspension framework, including surficial/core sediments and settling trap-collected particles (TCPs), was assessed in the Jiaozhou Bay (JZB) to examine the behavior and fate of particulate biogenic elements (C, N, P and Si). Resuspension-mediated differences in the concentrations of numerous biogenic proxies were significant and mainly corresponded to selective upwelling of fine-sized, nutrient-enriched particles, to autochthonous organic matter degradation below the trap-deployed level comprising water column transportation and long-term retention at the sediment-water interface. This is further reinforced by smaller inorganic carbon concentrations in sediments and origin-indicating stoichiometric ratio records (OC:ON, OC:OP). Nevertheless, biogenic silica (BSi) exhibited a near homologous concentration and had the largest preservation efficiency. Three principal components, representing production and preservation, remineralisation, and a particle-size effect, accounted for 55.5%, 14.0%, and 9.1% of the total variance, respectively. After calibration, the primary sinking flux was two orders of magnitude smaller than the measured absolute sedimenting flux. Also, the limited bottom achieving contribution with a maximum of 28.3% for freshly biogenic particles produced in autumn/winter circumstances with low primary productivity was inferred. The recurrent resuspension processes in JZB demonstrated that 5-12 cycles of similar or higher intensity resuspension was required before freshly-formed biogenic particles could ultimately be integrated into the sediments. Regarding the internal P sink-switching mechanism, the previously transformed Fe-bound fraction across the estuarine salinity gradient has limited application under offshore redox oscillations, whereas near-quantitative transfer of dissolved P from remineralized organic matter to authigenic carbonate fluorapatite could substantially reduce its bio-availability in resuspended particulate P.