Dynamic blood oxygenation level-dependent functional MRI was applied at 7 T in the rat olfactory bulb (OB) with pulsed delivery of iso-amyl acetate (IAA) and limonene. Acquisition times for singleslice and whole OB data were 8 and 32 s, respectively, with spatial resolution of 220 ؋ 220 ؋ 250 m. On an intrasubject basis, short IAA exposures of 0.6 min separated by 3.5-min intervals induced reproducible spatial activity patterns (SAPs) in the olfactory nerve layer, glomerular layer, and external plexiform layer. During long exposures (Ϸ10 min), the initially dominant dorsal SAPs declined in intensity and area, whereas in some OB regions, the initially weak ventral͞lateral SAPs increased first and then decreased. The SAPs of different concentrations were topologically similar, which implies that whereas an odor at various concentrations activates the same subsets of receptor cells, different concentrations are assessed and discriminated by variable magnitudes of laminarspecific activations. IAA and limonene reproducibly activated different subsets of receptor cells with some overlaps. Whereas qualitative topographical agreement was observed with results from other methods, the current dynamic blood oxygenation level-dependent functional MRI results can provide quantitative SAPs of the entire OB.blood oxygenation level-dependent ͉ functional mapping ͉ olfactory bulb I n mammals, olfactory behaviors such as determination of food palatability and searching require accurate assessment and discrimination of different odor types, concentrations, and exposure duration (1). Distinctions between these behavioral tasks are believed to rely on a spatial-encoding mechanism in which different odor and concentrations evoke spatial activity patterns (SAPs) in the olfactory bulb (OB). The SAPs are derived from functionally induced activity in olfactory receptor neurons that synapse at specific glomeruli (2).Insights into the coding of olfactory information have been partially inferred from SAPs in the OB, where the data can be obtained by various methods: 2-deoxyglucose autoradiography (3), electrophysiology (4), c-fos expression (5), functional MRI (fMRI) (6), and optical imaging of voltage-sensitive dyes (7) or intrinsic signals (8). Experimental limitations of each method affect data interpretations because each method maps a specific signal. Certain experimental criteria have to be met for olfactory perception to be systematically and ideally derived from the functional architecture revealed by the SAPs: (i) the neuroanatomy of the whole OB has to be mapped; (ii) the dynamic nature of SAPs in the whole OB has to be mapped with both high spatial and temporal resolutions; (iii) laminar-specific activations in the different layers have to be quantitated; and (iv) reproducibility of SAPs has to be established in a quantitative manner such that the effects of stimulus parameters (e.g., odor type, concentration, and exposure duration) can be easily identified and separated. If each criterion is met on an intrasubject basis by a par...