THE main advantage of confocal microscopes over their conventional cou
nterparts arises from their ability to optically 'section' nearly tran
sparent materials; the thin image slices thus obtained can be used to
reconstruct three-dimensional images, a capability which is particular
ly useful for the study of biological specimens, Confocal microscopes
have previously used either a single laser-illuminated point-source an
d single point-detector (which are scanned in tandem across the object
) or white-light illumination with multiple point-sources and detector
s, Single-point-source systems, however, do not usually form images in
real time and are restricted to using available laser wavelengths, Mu
ltiple-point-source systems, on the other hand, produce images in real
time but use light very inefficiently-typically 1% or less is used fo
r imaging, Here we demonstrate a white-light, multiple-point-source me
thod which can in principle produce images in real time,vith light eff
iciencies as high as 50%. This system is likely to find broad practica
l application, particularly in the imaging of weakly reflecting or wea
kly fluorescent specimens.