The perirhinal and entorhinal cortices are critical components of the medial temporal lobe (MTL) declarative memory system. Study of their specific functions using blood oxygenation level-dependent (BOLD) functional magnetic resonance imaging (fMRI), however, has suffered from severe magnetic susceptibility signal dropout resulting in poor temporal signal-to-noise (tSNR) and thus weak BOLD signal detectability. We have demonstrated that higher spatial resolution in the z-plane leads to improved BOLD fMRI signal quality in the anterior medial temporal lobes when using a 16-element surface coil array at 3 T (Tesla). Using this technique, the present study investigated the roles of the anterior medial temporal lobe, particularly the entorhinal and perirhinal cortices, in both object and spatial memory. Participants viewed a series of fractal images and were instructed to encode either the object's identity or location. Object and spatial recognition memory were tested after 18-sec delays. Both the perirhinal and entorhinal cortices were active during the object and spatial encoding tasks. In both regions, object encoding was biased to the left hemisphere, whereas spatial encoding was biased to the right. A similar hemispheric bias was evident for recognition memory. Recent animal studies suggest functional dissociations among regions of the entorhinal cortex for spatial vs. object processing. Our findings suggest that this process-specific distinction may be expressed in the human brain as a hemispheric division of labor.Studies in rodents and monkeys are suggestive of a process-specific division of labor within the perirhinal and entorhinal cortices. For example, electrophysiological and lesion studies in rodents show that within the entorhinal cortex more medial subdivisions receive and process spatial information, whereas lateral regions receive and process object-related information (Fyhn et al. 2004;Hafting et al. 2005;Hargreaves et al. 2005;Seffenach et al. 2005;Kerr et al. 2007).Correspondingly, in the monkey, the dorsal and ventral visual processing streams have different projection paths along the rostro-caudal extent of the parahippocampal cortex, perirhinal, entorhinal cortex and throughout the perforant pathway to the hippocampus Amaral 1994, 2004;Suzuki et al. 1997;Burwell 2000;Munoz and Insausti 2005). Superimposed upon this rostro-caudal topography are medial to lateral afferent projection gradients within both perirhinal and entorhinal cortices (Saleem and Tanaka 1996;Mohedano-Moriano et al. 2007). Although functional dissociations between the medial and lateral regions of these cortical structures have yet to be demonstrated, the anatomical connectivity is suggestive of a medial to lateral functional distinction in the monkey similar to that found in rodents.In humans, both neuropsychological (e.g., Kimura 1963;Milner 1972;Glosser et al. 1995;Jones-Gotman et al. 1997;Bohbot et al. 2000;Kelley et al. 2002;Kennepohl et al. 2007) and neuroimaging (e.g., Moscovitch et al. 1995;Martin et al. 1997;Bellg...