The distribution and concentration of elements, both essential and nonessential, within plant tissues change over time in response to physiological stimuli, developmental stage, and the external environment. To improve the understanding of genetic and physiological processes controlling plant growth, it is necessary to understand these changes both statically and dynamically at the tissue, cellular, and subcellular levels. The distribution of elements within plant tissues is informative for studies ranging from functional characterization in molecular biology, improving human nutrition, improving plant health and climate adaptability, to the movement and toxicity of contaminants throughout the food chain. The range of methods suitable for examining the concentration and distribution of elements within plants includes x-ray fluorescence microscopy (XFM), scanning electron microscopy coupled with energydispersive x-ray spectroscopy, nanoscale secondary ion mass spectrometry, laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), microparticleinduced x-ray emission, confocal microscopy with fluorophores, and autoradiography with radioactive isotopes. These various techniques all have advantages and disadvantages, differing not only in the extent of sample preparation required but also in sensitivity (detection limit), resolution, detectable elements, and probed volume (Lombi et al., 2011b). Of particular