With the increasing use of molecular genetic techniques in ecology and evol
ution, it has become apparent that methods of non-destructive DNA sampling
must be developed. In this study we collected 50 blue mussels (Mytilus spp.
) in each of three size categories: small (10-20 mm), medium (20-30 mm), an
d large (30+ mm). Hemolymph was extracted from 25 mussels in each size cate
gory and the remaining 25 mussels served as controls. The hemolymph was ext
racted and control mussels were monitored for 384 days, during which Lime n
o significant differences in survival or growth were found. We extracted DN
A from the hemolymph and successfully polymerase chain reaction-amplified t
he TTS and Glu-5' species-specific markers from 81% and 92% of the samples.
respectively, and determined that all mussels were Mytilus trossulus (Lama
rck). The extraction of hemolymph for DNA analysis allows for molecular inv
estigations of populations ur species which are either rare or in limited n
umbers, and for life history investigations where survival of the organism
is necessary.