| REAL-TIME PCR ASSAYS FOR THE
DETECTION OF HAB SPECIES FROM
BRACKISH LAGOONAL PONDS IN SOUTH CAROLINA,
USA
Workshop on Real-time Coastal Observing Systems
for Ecosystem Dynamics and Harmful
Algal Blooms. Villafranche-sur mer, France. 11-21 June 2003.
Jason
W. Kempton1,
Patrick Williams2, Susan B. Wilde2, and Alan J.
Lewitus1,
2
South
Carolina
Department of Natural Resources, Marine Resources Research Institute,
217 Ft.
Johnson Road, Charleston, SC 29412, USA; Belle W. Baruch Institute for
Coastal
Research, University of South Carolina, P.O. Box 1630, Georgetown, SC
29442,
USA
In 2001, the South
Carolina Harmful Algal Bloom Program
(SCHABP) extended its surveillance efforts to include brackish lagoonal
retention ponds associated with housing developments and golf courses.
These
ponds are numerous along the South Carolina (SC), USA
coast (> 1500 ponds over 1 acre) and are routinely used for
recreational
activities (fishing, crabbing, swimming, skiing). They are also
hypereutrophic,
and our results suggest that they are “natural incubators” for HABs.
From
2001-2002, 107 blooms from 9 different HAB species (Chattonella
subsalsa,
Chattonella verruculosa, Fibrocapsa japonica, Heterosigma akashiwo,
Karlodinium
micrum, Kryptoperidinium foliaceum, Pfiesteria piscicida, Pfiesteria
shumwayae,
and Prymnesium parvum) were documented in SC brackish
ponds. With
the exception of K. foliaceum, none of these were known to form
blooms
in SC. Several of these blooms were associated with fish kills and/or
measurable toxic activity. Rapid
quantitative detection of these HAB species is of central importance to
facilitate understanding bloom ecology and direct proper response.
Here, we
describe the application of real-time PCR assays for the detection of
several
HAB species recently observed in SC waters. Real-time PCR offers a
rapid,
sensitive means of detecting HAB species, and can provide quantitative
information with appropriate “ground-truthing”. Real-time PCR has been
incorporated into SCHABP routine monitoring and fish kill response
protocols,
and integrated with microscopic and HPLC pigment analyses to provide
accurate
assessment of HAB species identity.
|