Comparison of 18S ribosomal RNA gene sequences between diverse bivalve spec
ies, including eight scallop species, allowed the design of an 18S rRNA tar
geted oligonucleotide probe (BS-1364) that tvas specific for scallops belon
ging to the genus Argopecten (bay and calico scallops). The high sequence s
imilarity of the 18S rRNA gene between Argopecten irradians and Argopecten
gibbus (98.8%) prevented the design of an A. irradians species-specific pro
be. Hybridization studies using amplified 18S rDNA from a diverse collectio
n of bivalve species demonstrated that the specificity of the digoxygenin-l
abeled probe was consistent with the predicted specificity indicated by seq
uence comparison. Hybridization studies using laboratory-spawned bay scallo
p veligers indicated that a single veliger could be detected by probe hybri
dization in a blot format, and that probe hybridization signal was proporti
onal (r(2) = .99) to the abundance of veligers. Methods for rRNA extraction
and blotting were developed that allowed bay scallop veligers to be specif
ically and quantitatively identified in natural plankton samples. Prelimina
ry studies conducted in Tampa Bay, Florida, suggest that introduced scallop
s can successfully spawn and produce veligers under in situ conditions. The
Argopecten-specific probe and methods developed in this study provide the
means to study the production and fate of bay scallop larvae in nature and
provide evidence that scallops introduced into Tampa Bay have the potential
for successful reproduction and enhancement of scallop stocks.