Lignin distribution in the tracheid cell wall of mild compression wood in P
inus radiata D. Don was examined by interference microscopy, confocal fluor
escence microscopy, and ultraviolet (UW) microscopy. Two anatomically diffe
rent samples of mild compression wood were compared with a sample of normal
wood using quantitative interference microscopy and microdensitometry comb
ined with confocal fluorescence microscopy to estimate the quantitative or
semiquantitative lignin distribution in the S2 and S2(L) regions of the sec
ondary cell wall and of the cell corner middle lamella (CCML). One of these
samples was briefly examined by UV microscopy for comparison. Quantitative
interference microscopy provided information on lignin concentration in di
fferent regions of the cell wall with values of 26, 46, and 57%, respective
ly, for the S2, S2(L), and CCML regions of sample 1 and 20, 29, and 46%, re
spectively, for the same regions of sample 2. Microdensitometry of confocal
fluorescence images provided semiquantitative information on the relative
lignin distribution based on lignin autofluorescence. Comparison between th
e two compression wood samples using autofluorescence gave results that wer
e in partial agreement with interference microscopy with respect to the rel
ative lignification levels in the S2, S2(L), and CCML regions. Some improve
ment was achieved by using calibration values for hemicellulose rather than
holocellulose for interference data in the S2, region. Results for UV micr
oscopy performed on sample 1 indicated that the lignification of the CCML r
egion was comparable with that of the S2(L) region in this sample but with
some variation among cells. All three techniques indicated significant vari
ation in lignification levels of the S2(L) and CCML regions among adjacent
cells and a significant reduction in the lignification of the CCML region c
ompared to normal wood.