Groundwater (GW) contaminants upwelling toward surface water (SW) can attenuate in the hyporheic zone, with dissolved oxygen (DO) frequently controlling the attenuation. In a laboratory mesocosm, we induced downwelling of SW into the sediments to create a hyporheic flow cell (HFC). We added DO to downwelling SW and sodium sulfite (Na 2 SO 3) to anoxic upwelling GW to induce an abiotic mixing-dependent reaction along the mixing zone between the HFC and upwelling GW. Using planar optodes and SO 4 measurements, we observed movement of the DO mixing zone (oxic front position), extent of DO mixing (mixing zone thickness), and location of MD reaction (SO 4 peak concentration). Oxic front position and mixing zone thickness were stable during nonreactive control experiments, indicating that dispersion of DO across the mixing zone had come into equilibrium with supply of DO to the mixing zone. By contrast, mixing zone thickness shrank over time during the reaction experiments, as MD reaction consumed DO in the mixing zone. The decrease in mixing zone thickness for the reaction experiments indicates steeper DO gradients and greater dispersion (transport) limitation, quantified by Damköhler numbers farther above unity. Maximum SO 4 concentrations always occurred further from the center of the HFC (i.e., more toward surrounding upwelling GW) than did the oxic front. In most riverbeds, transport and mixing dynamics are thus superimposed upon existing hydraulic dynamics, with implications for monitoring and attenuation of contaminants. Plain Language Summary Groundwater (GW) contaminants approaching surface water (SW) can be removed in shallow sediments (hyporheic zone), with dissolved oxygen (DO) frequently a controlling factor in the removal. These reactions sometimes require mixing of chemicals coming from SW and GW. We simulated such a mixing zone in shallow laboratory sediments, including (1) a nonreactive control experiment where DO coming from SW mixed with water without DO coming from deeper GW and (2) a nonbiological mixing-dependent reaction of sodium sulfite (Na 2 SO 3) in GW with DO in SW to produce sulfate (SO 4). We found that the concentration patterns for the control experiments were stable over time, but those for the reaction experiments were more dynamic. This was confirmed by differences in location of peak product (SO 4) concentration and that of the current DO mixing zone. Thus, in most riverbeds, transport and mixing dynamics are superimposed upon hydraulic dynamics, with implications for monitoring and attenuation of GW contaminants approaching surface water.