Dl. Wetzel et al., ULTRASPATIALLY-RESOLVED SYNCHROTRON INFRARED MICROSPECTROSCOPY OF PLANT-TISSUE IN-SITU, Cellular and molecular biology, 44(1), 1998, pp. 145-168
Routine use of 6 mu m or 12 mu m apertures with synchrotron microspect
roscopy provide good spectra without excessive co-addition of scans. 1
00% mapping by stepping in pixel sized increments reveals chemical het
erogeneity within cellular dimensions. The brightness of the synchrotr
on source and the absence of thermal noise compared to a conventional
thermal (globar) source yields favorable signal-to-noise operation. Th
e nondivergent characteristics of the source result in minimal loss of
radiation at the aperture, hence, spatial resolution approaches the d
iffraction limit. Details of cellular dimensions are then localized wi
thin any maps produced and individual spectra obtained from adjacent p
ixels clearly shows the striking difference in chemistry even within a
microscopic vicinity. In this report the mapping of plant tissue with
the synchrotron is contrasted to previous lower spatial resolution ma
pping experiments done with the globar on similar materials using inte
rpolation between separated sampling spots and larger apertures.