Does visual working memory represent a fixed number of objects, or is capacity reduced as object complexity increases? We measured accuracy in detecting changes between sample and test displays and found that capacity estimates dropped as complexity increased. However, these apparent capacity reductions were strongly correlated with increases in sample-test similarity (r= .97), raising the possibility that change detection was limited by errors in comparing the sample and test, rather than by the number of items that were maintained in working memory. Accordingly, when sample-test similarity was low, capacity estimates for even the most complex objects were equivalent to the estimate for the simplest objects (r= .88), suggesting that visual working memory represents a fixed number of items regardless of complexity. Finally, a correlational analysis suggested a two-factor model of working memory ability, in which the number and resolution of representations in working memory correspond to distinct dimensions of memory ability.

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The functional organization of human auditory cortex has not yet been characterized beyond a rudimentary level of detail. Here, we use functional MRI to measure the microstructure of orthogonal tonotopic and periodotopic gradients forming complete auditory field maps (AFMs) in human core and belt auditory cortex. These AFMs show clear homologies to subfields of auditory cortex identified in nonhuman primates and in human cytoarchitectural studies. In addition, we present measurements of the macrostructural organization of these AFMs into "clover leaf" clusters, consistent with the macrostructural organization seen across human visual cortex. As auditory cortex is at the interface between peripheral hearing and central processes, improved understanding of the organization of this system could open the door to a better understanding of the transformation from auditory spectrotemporal signals to higher-order information such as speech categories.tonotopy | periodotopy | cochleotopy | temporal receptive field | traveling wave H umans have evolved a highly sophisticated auditory system for the transduction and analysis of acoustic information, such as the spectral content of sounds and the temporal modulation of sound energy. The basilar membrane of the cochlea is organized tonotopically to represent the spectral content of sounds from high to low frequencies. This tonotopic (or cochleotopic) organization is preserved as auditory information is processed and passed on from the cochlea to the superior olive, the inferior colliculus, the medial geniculate nucleus, and into primary auditory cortex. Such cortical preservation of the peripheral sensory topography creates a common topographic sensory matrix in hierarchically organized sensory systems, important for consistent sensory computations. The current state of knowledge of the functional organization of human auditory cortex indicates the existence of multiple cortical subfields organized tonotopically. However, the number of these human cortical subfields, their boundaries, and their orientations relative to anatomical landmarks remain equivocal, due in part to an inability to measure cortical representations of a second acoustic dimension orthogonal to tonotopy to accurately delineate them.This ambiguity of human auditory subfield definitions contrasts dramatically with the current understanding of the functional organization of human visual cortex, in which detailed maps of the organization of the retina, called visual field maps (VFMs), have been well characterized (1-9). In vision, there are two orthogonal dimensions of visual space, eccentricity and polar angle, which together allow for the mapping of cortical representations to unique locations in visual space and the complete delineation of the boundaries of individual visual field maps. In audition, there has been only one dimension of sensory topography clearly mapped in cortex, which makes it impossible to use sensory topography to accurately differentiate specific human cortical auditory field maps (AFM...

Crowding refers to the phenomenon in which nearby distractors impede target processing. This effect is reduced as target-distractor distance increases, and it is eliminated entirely at a distance that is labeled the critical spacing point. Attention, distractor preview, and popout are each known to facilitate processing in crowded displays. Eight experiments examined whether this is accomplished via a reduction in critical spacing. Attention was manipulated via spatial cueing, whereby a peripheral cue elicited a stimulus-driven shift of attention. Distractor preview was examined by manipulating whether the crowding distractors were presented prior to or simultaneous with the target. Popout was examined by manipulating whether there was a salient color difference between the target and distractors. As demonstrated in previous studies, we found robust benefits of spatial cueing, preview, and popout in crowded displays. However, although spatial cueing led to robust improvements in target discrimination, there was no reduction in critical spacing for attended stimuli. By contrast, both preview and popout caused large reductions in critical spacing. These disparate results indicate that attention improves target discrimination in crowded displays in a qualitatively different manner than do the other factors.

Although several studies have suggested that cortical alterations underlie such age-related visual deficits as decreased acuity, little is known about what changes actually occur in visual cortex during healthy aging. Two recent studies showed changes in primary visual cortex (V1) during normal aging; however, no studies have characterized the effects of aging on visual cortex beyond V1, important measurements both for understanding the aging process and for comparison to changes in age-related diseases. Similarly, there is almost no information about changes in visual cortex in Alzheimer's disease (AD), the most common form of dementia. Because visual deficits are often reported as one of the first symptoms of AD, measurements of such changes in the visual cortex of AD patients might improve our understanding of how the visual system is affected by neurodegeneration as well as aid early detection, accurate diagnosis and timely treatment of AD. Here we use fMRI to first compare the visual field map (VFM) organization and population receptive fields (pRFs) between young adults and healthy aging subjects for occipital VFMs V1, V2, V3, and hV4. Healthy aging subjects do not show major VFM organizational deficits, but do have reduced surface area and increased pRF sizes in the foveal representations of V1, V2, and hV4 relative to healthy young control subjects. These measurements are consistent with behavioral deficits seen in healthy aging. We then demonstrate the feasibility and first characterization of these measurements in two patients with mild AD, which reveal potential changes in visual cortex as part of the pathophysiology of AD. Our data aid in our understanding of the changes in the visual processing pathways in normal aging and provide the foundation for future research into earlier and more definitive detection of AD.

Are resources in visual working memory allocated in a continuous or a discrete fashion? On the one hand, flexible resource models suggest that capacity is determined by a central resource pool that can be flexibly divided such that items of greater complexity receive a larger share of resources. On the other hand, if capacity in working memory is defined in terms of discrete storage "slots" then observers may be able to determine which items are assigned to a slot but not how resources are divided between stored items. To test these predictions, we manipulated the relative complexity of the items to be stored while holding the number items constant. Although mnemonic resolution declined when set size increased (Experiment 1), resolution for a given item was unaffected by large variations in the complexity of the other items to be stored when set size was held constant (Experiments 2-4). Thus, resources in visual working memory are distributed in a discrete slot-based fashion, even when inter-item variations in complexity motivate an asymmetrical division of resources across items.

One of the fundamental properties of the mammalian brain is that sensory regions of cortex are formed of multiple, functionally specialized cortical field maps (CFMs). Each CFM comprises two orthogonal topographical representations, reflecting two essential aspects of sensory space. In auditory cortex, auditory field maps (AFMs) are defined by the combination of tonotopic gradients, representing the spectral aspects of sound (i.e., tones), with orthogonal periodotopic gradients, representing the temporal aspects of sound (i.e., period or temporal envelope). Converging evidence from cytoarchitectural and neuroimaging measurements underlies the definition of 11 AFMs across core and belt regions of human auditory cortex, with likely homology to those of macaque. On a macrostructural level, AFMs are grouped into cloverleaf clusters, an organizational structure also seen in visual cortex. Future research can now use these AFMs to investigate specific stages of auditory processing, key for understanding behaviors such as speech perception and multimodal sensory integration.