The large spatial inhomogeneity in transmit B 1 field (B 1 + ) observable in human MR images at high static magnetic fields (B 0 ) severely impairs image quality. To overcome this effect in brain T 1 -weighted images, the MPRAGE sequence was modified to generate two different images at different inversion times, MP2RAGE. By combining the two images in a novel fashion, it was possible to create T 1 -weigthed images where the result image was free of proton density contrast, T 2 ⁎ contrast, reception bias field, and, to first order, transmit field inhomogeneity. MP2RAGE sequence parameters were optimized using Bloch equations to maximize contrast-to-noise ratio per unit of time between brain tissues and minimize the effect of B 1 + variations through space. Images of high anatomical quality and excellent brain tissue differentiation suitable for applications such as segmentation and voxel-based morphometry were obtained at 3 and 7 T. From such T 1 -weighted images, acquired within 12 min, high-resolution 3D T 1 maps were routinely calculated at 7 T with sub-millimeter voxel resolution (0.65-0.85 mm isotropic). T 1 maps were validated in phantom experiments. In humans, the T 1 values obtained at 7 T were 1.15 ± 0.06 s for white matter (WM) and 1.92 ± 0.16 s for grey matter (GM), in good agreement with literature values obtained at lower spatial resolution. At 3 T, where whole-brain acquisitions with 1 mm isotropic voxels were acquired in 8 min, the T 1 values obtained (0.81 ± 0.03 s for WM and 1.35 ± 0.05 for GM) were once again found to be in very good agreement with values in the literature. © 2009 Elsevier Inc. All rights reserved. IntroductionIn the past decade, the magnetization-prepared rapid gradient echo, MPRAGE (Mugler and Brookeman, 1990), sequence has become one of the most commonly used sequences to obtain T 1 -weighted anatomical images of the human brain, in particular at high magnetic field. MPRAGE images are routinely used as anatomical reference for fMRI or for brain tissue classification in voxel-based morphometry (Ashburner and Friston, 2000). However, at high static magnetic fields (≥ 3 T), the increased inhomogeneity of the transmit B 1 + and receive B 1 − fields creates intensity variations throughout the image (bias field). Bias fields not only render segmentation and quantitative analysis difficult but also severely affect image quality at ultra-high fields (≥7 T). The use of adiabatic pulses to perform the inversion in the MPRAGE is only partially able to mitigate the effects of inhomogeneous B 1 . A number of strategies have been proposed to minimize or to correct bias fields generated by the inhomogeneity of the B 1 fields. Most correction strategies aim at correcting the combined (transmit and receive) bias field via post-processing techniques. This can be done either by low-pass filtering (Cohen et al., 2000;Wald et al., 1995) or by fitting slowly varying functions such as Gaussians or low order polynomials (Styner et al., 2000). The result from these low pass filters or fits is then su...

The primary auditory cortex (PAC) is central to human auditory abilities, yet its location in the brain remains unclear. We measured the two largest tonotopic subfields of PAC (hA1 and hR) using high-resolution functional MRI at 7 T relative to the underlying anatomy of Heschl's gyrus (HG) in 10 individual human subjects. The data reveals a clear anatomical-functional relationship that, for the first time, indicates the location of PAC across the range of common morphological variants of HG (single gyri, partial duplications, and complete duplications). In 20/20 individual hemispheres, two primary mirror-symmetric tonotopic maps were clearly observed with gradients perpendicular to HG. PAC spanned both divisions of HG in cases of partial and complete duplications (11/20 hemispheres), not only the anterior division as commonly assumed. Specifically, the central union of the two primary maps (the hA1-R border) was consistently centered on the full Heschl's structure: on the gyral crown of single HGs and within the sulcal divide of duplicated HGs. The anatomicalfunctional variants of PAC appear to be part of a continuum, rather than distinct subtypes. These findings significantly revise HG as a marker for human PAC and suggest that tonotopic maps may have shaped HG during human evolution. Tonotopic mappings were based on only 16 min of fMRI data acquisition, so these methods can be used as an initial mapping step in future experiments designed to probe the function of specific auditory fields.

To study the properties of human primary somatosensory (S1) cortex as well as its role in cognitive and social processes, it is necessary to noninvasively localize the cortical representations of the body. Being arguably the most relevant body parts for tactile exploration, cortical representations of fingers are of particular interest. The aim of the present study was to investigate the cortical representation of individual fingers (D1-D5), using human touch as a stimulus. Utilizing the high BOLD sensitivity and spatial resolution at 7T, we found that each finger is represented within three subregions of S1 in the postcentral gyrus. Within each of these three areas, the fingers are sequentially organized (from D1 to D5) in a somatotopic manner. Therefore, these finger representations likely reflect distinct activations of BAs 3b, 1, and 2, similar to those described in electrophysiological work in non-human primates. Quantitative analysis of the local BOLD responses revealed that within BA3b, each finger representation is specific to its own stimulation without any cross-finger responsiveness. This finger response selectivity was less prominent in BA 1 and in BA 2. A test-retest procedure highlighted the reproducibility of the results and the robustness of the method for BA 3b. Finally, the representation of the thumb was enlarged compared to the other fingers within BAs 1 and 2. These findings extend previous human electrophysiological and neuroimaging data but also reveal differences in the functional organization of S1 in human and nonhuman primates. Hum Brain Mapp 35:213-226,

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