This paper reports on a study in which fine seawater droplets were placed on zinc surfaces for periods of 15 min to 6 h. After each exposure, droplets were either extracted from the specimens or allowed to evaporate in laboratory conditions. Scanning electron microscopy ͑SEM͒-energy-dispersive spectroscopy, X-ray microdiffraction, and SEM-focused ion beam studies were undertaken on the specimens after exposure, as was in situ Raman spectroscopy on zinc covered with a saline droplet. Approximately 30 min after droplets were placed on the surface, a thin moisture layer ͑termed the secondary spreading film͒ spread out from the central droplet. As a function of position and time, oxide development in the central region was initially slow; however, after ϳ30 min, a significant local attack of the underlying microstructure occurred. Correspondingly, precipitate phases developed on top of the oxide, which produced an oxide consisting of three bands: an irregular zone with a localized metal attack and significant voids at the metal/oxide interface, overlaid by a relatively void-free layer, which in turn was overlaid by a porous zone. At the edge of the drop ͑before the secondary spreading͒, oxide growth was much faster, and the deposition of phases that precipitate in solutions appeared critical. We discuss the chemistry and identification of the various phases and the implications of oxide formation to the electrochemical processes occurring in drops.While Part I of this two-part series 1 looked at the formation of oxides on polished zinc surfaces after 1 and 2.5 day exposures to seawater droplets, here we explore oxide formation after short exposures. This paper analyzes oxide formation at the "surface" using X-ray microdiffraction ͑XRD͒ and scanning electron microscopyenergy-dispersive spectroscopy ͑SEM-EDS͒, as well as in sections through the oxide using SEM-focused ion beam ͑FIB͒. We also look at in situ oxide development using Raman spectroscopy.Part I included an extensive review of the literature on the formation of oxides, which is not repeated here. However, observations on the very early development of surface oxides are pertinent to this paper. In studies involving surface analysis under droplets, thin films in solution 2,3 or in field exposures, 4 several authors have reported a sequence whereby the initial zinc oxide is transformed to zinc hydroxide, and then a zinc carbonate ͑or zinc hydroxy carbonate͒ layer forms on top before a final layer of zinc hydroxy anions forms ͑the exact zinc hydroxy anion depends on the environment but is commonly zinc hydroxyl-chloride or zinc hydroxyl-sulfate͒. Most of these studies were after exposures from hours to days for the laboratory experiments and for days to years in the field exposure. In Part I, 1 it was reported that the application of a 0.5 L seawater drop under high relative humidity ͑RH͒ exhibited secondary spreading, with the central region initially acting as an anode and the outer region initially acting as a cathode. When a drop is initially placed on a sur...