In recent years much attention has focused on the preservation of dino
saur bone.(1-3) In such molecular palaeontological studies contaminati
on of ancient DNA by human DNA is a major concern, yet contamination b
y contemporary plants and organisms may pose an even more serious prob
lem since sequences amplified from such material would be less likely
to be recognised as contaminants. In this study, we report several mic
roscopic fragments of fossil wood located within the marrow cavity of
a hypsilophodontid femur from the Early Cretaceous Otway Group, Dinosa
ur Cove, south-eastern Australia.(3) The wood is not recognisable macr
oscopically and it was only identified as such by thin sectioning proc
edures and light microscopy. Thus, if this sample was pulverised for D
NA extraction, the extreme sensitivity of the polymerase chain reactio
n (PCR) technique could result in amplification of DNA templates of ei
ther or both the dinosaur and the wood. The specificity of the PCR app
roach should normally preclude amplification of non-animal DNA.(2) How
ever in order to amplify ancient and degraded DNA samples successfully
it may be necessary to lower the annealing temperature to a level whe
re this specificity becomes compromised.