1. INTRODUCTION
The acquired MRSI signal is conventionally modeled as {\mbi s}({\mbi k}, t)=\int \int\rho({\mbi r}, f)e^{-i2\pi {\mmb k}\cdot {\mmb r}}e^{-i2\pi ft}d{\mbi r}df+\xi({\mbi k}, t), \eqno{\hbox{(1)}}where denotes the desired spatial-spectral function and represents the measurement noise often modeled as a complex white Gaussian process. The function contains valuable information on the spatial-spectral distribution of metabolites, and is useful for noninvasive metabolite imaging of living systems. For example, MRSI can be used to study glucose metabolism [1]; MRSI can map out the spatial distributions of N-Acetyl aspartate (NAA), creatine, choline, and lactate metabolites that are useful for the investigation of neurological disorders [2]. However, considerable practical challenges remain in obtaining in both high spatial-spectral resolution and high SNR. These difficulties are due to acquisition time limitations and low concentrations of metabolites (typically thousands-fold below that of tissue water [3]). This paper addresses the low SNR problem.