SummaryThe recommended procedures for melissopalynology suffer from two problems that can lead to incorrect assignment of honey origin. One problem is the Jack of complete sedimentation of the pollen from honey samples owing to centrifugation of too concentrated a solution for too short a time at too low a centrifuge speed. This can result in selective sedimentation of larger, more dense pollen grains. The other problem with recommended melissopalynology procedures is a lack of insistence that all samples be subjected to an acetolysis procedure. An example of this problem with identification is given where willow and rapeseed (canola) pollen appear virtually identical before acetolysis, but can be seen as markedly different afterwards.
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Low et al. (1989) studied this question.
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