HARMFUL ALGAE BLOOM (HAB) RESEARCH

2016 Pilot Study

Cochlodinium polyrikoides is a commonly occurring species of harmful algae species seen in coastal regions globally (Lee and Lee, 2006; Tang and Gobler, 2008; Park et al., 2015; Kim et al., 2016). Harmful algae blooms (HABs), such as C. Poly blooms, occur in coastal regions and can have serious negative effects on commercial wild and aquacultured species (Tang et al., 2004; O’Neil et al., 2012). HAB events are increasing globally in frequency, maginitude and toxicity, and are estimated to have an economic effect of approximately USD $50 million annually in the United States (Hoagland et al., 2002; Jeong et al., 2008; Park et al., 2013).

C. poly blooms, or brown tides, have been increasing in distribution, duration, and frequency globally, including in the United States (Hoagland et al., 2002; Garate-Lizarraga et al., 2003; Rountos et al., 2014). C. poly is non-toxic to humans, but can have serious effects on juvenile shellfish and finfish, and is known to cause fish/shellfish kills globally (Lee and Lee, 2006; Gobler et al., 2008; Tang and Gobler, 2009). For Juvenille shellfish, such as bay scallops (Argopecten irradians) and American oysters (Crassostrea virginica), C. poly bloom events result in high mortality during blooms and reduced growth rates following blooms (Gobler et al., 2008; Tang and Gobler, 2008; Tang and Gobler, 2009).

In 2016, Ward Aquafarms, conducted a study during a C. poly bloom in Buzzard’s Bay and Fiddler’s Cove Marina in North Falmouth, MA. C. poly cell concentrations were calculated by obtaining water samples aforementioned locations and then performing C. poly cell counts. C. poly distribution and cell densities were documented in Fiddler’s Cove (nursery area) and Buzzard’s Bay, with C. poly cell densities highest in Fiddler’s Cove Marina adjacent to Ward Aquafarms shellfish nursery systems.

Ward Aquafarms also tracked the survival and growth rates of adult and juvenile oysters, clams and bay scallops during the 2016 C. poly bloom. With the C. poly cell densities highest adjacent to Ward Aquafarms’ oyster and bay scallop nursery systems in Fiddler’s Cove Marina, Ward Aquafarms was able to document what any negative effects in survival and growth caused by high concentrations of C. poly.

After 60 days, reductions in growth rates and survival for juvenile (< 10 mm) bay scallops, clams and oysters in the nursery systems were observed during the 2016 bloom. Juvenile oysters less than 10 mm had a mean±SD percent survival 49.9±5.4% and mean±SD growth rate of 0.03±0.0 mm/day. Juvenile oysters greater than 10 mm had a survival rate of 94.9±3.6% and a growth rate of 0.40±0.1 mm/day. Since C. poly densities were highest in the nursery area, and nursery size bay scallops, clams, oysters are the most impacted by C. poly blooms, strategies to mitigate the effects in the nursery area is of utmost importance. The results from Ward Aquafarms’ 2016 C. poly study launched a series of subsequent research on way to identify when a bloom is happening, how bad the bloom is, and ways to potentially mitigate the negative effects of a bloom.

Imaging FlowCytoBot (IFCB)

In 2017 and 2018 McLane Research Laboratories and Dr. Brosnahan (WHOI) partnered with Ward Aquafarms to determine strategies to mitigate HAB impacts on farmers, including early notification, ongoing monitoring, and farm management strategies. A cornerstone to these strategies is a new technology – called Imaging FlowCytobot (or IFCB) - that provides continuous, real-time, automated monitoring of the phytoplankton community around farms. Data produced by this sensor provide a massive leap forward for basic understanding and management of coastal ecosystems, while also informing managers, farmers and other stakeholder when a HAB is starting, growing or subsiding – all critical information to those aiming to mitigate HAB impacts.

The IFCB sensor is a submersible imaging-in-flow cytometer that acts as an automated microscope, collecting images of individual phytoplankton at up to 12 cell per second. Raw data from the instrument (~100,000 images a day)provides estimates of algae species’ concentrations and indicates physiological changes and important ecological interactions between species. Computer automated characterization of these types of changes can inform forecasts of a given species’ or bloom’s trajectory, ultimately providing farmers information about whether a HAB is increasing or waning so that they can act accordingly to protect their animals

The intent of the proposed project is to build on these preliminary results and to expand the benefits of real-time in situ microscopy and automated analysis software to farmers throughout the region. When farmers can be notified of bloom activity within the area of their farm, mitigation strategies such as moving shellfish to deeper water or areas of higher flow can be evaluated in terms of cost and permitting required. While it may be more labor intensive, if the shellfish can be moved either vertically within the water column, or to an adjacent water body, it often can be the difference between high mortality and low growth or a strong season which allows the farm to maintain economic viability.

In the summer of 2017, the project team completed a pilot IFCB deployment within the Ward Aquafarms nursery area in the same location. Immediate identification of C. polykrikoides when the IFCB was installed on July 28, 2017 led Dr. Ward to move juvenile oysters to an alternative grow site where harmful algal concentrations were much lower.  This action spared the farm from a much more significant loss of juvenile shellfish and demonstrated how knowledge of ongoing blooms can improve the profitability of the both the farm and its immediate neighbors. Future deployments of an IFCB will provide data and analytical products freely to farmers, managers, and other local and regional partners while also providing a needed data stream to prove a new automated system for protection of animals from C. polykrikoides exposure.

An initial classifier developed from the 2017 data set already shows great promise for automation of data analysis and will only improve with the collection of more images that better capture the variety of species that may co-occur with C. polykrikoides in the region.

Further refinement is also expected to enable discrimination of different C. polykrikoides cells types including vegetative and sexual forms, automatically and in real time, so that farmers can factor this information into decisions regarding nursery movements and other mitigation actions.

Environmental Monitoring App

In addition to the installation of the IFCB adjacent to Ward Aquafarms’ nursery systems, Ward Aquafarms has built a custom nursery monitoring and alert system, which measures chlorophyll, dissolved oxygen, water temperature, and flow rate for each system (YSI EXO3 sonde). With the suite of environmental factors provided by the YSI sonde in addition to the information provided by the IFCB, Ward Aquafarms can identify when a HAB is happening, shut off the nursery pumps, and monitor the water quality of the nursery system until the bloom has subsided. The nursery monitoring system and will alert the user if a given parameter has dropped below a user-specified threshold.

Due to the fact that the IFCB records the full diversity of phytoplankton within its 10-100 μm target size range, the sensor is also invaluable for monitoring other HAB species as well. A prime example is Pseudo-nitzschia spp., a group of diatoms that produce domoic acid, a toxin that causes amnesic shellfish poisoning when cells and/or their toxins are concentrated in shellfish meats. While toxic Pseudo-nitzschia blooms are well established threats in maritime Canada and along the U.S. west coast, it is only in recent years that the blooms have endangered New England shellfish resources, causing fall and winter closures and two shellfish recalls in Maine and precautionary harvest closures in Massachusetts and Rhode Island in 2016 and 2017.

Sources:

Anderson, D.M., Hoagland, P., Kaoru, Y. and White, A.W. 2000. Estimated annual economic impacts from harmful algal blooms (HABs) in the United States. WHOI-2000-11. Department of Biology, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts.

Garate-Lizarraga, I., Lopez-Cortes, D.J., Bustillos-Guzman, J.J., Hernandez-Sandoval, F. 2003. Blooms of Cochlodinium polykrikoides (Gymnodiniaceae) in the Gulf of California, Mexico. Revista de Biologia Tropical. 52(1):51-58.

Gobler, C.J., Berry, D.L., Anderson, O.R., Burson, A., Koch, F., Rodgers, B.S., Moore, L.K., Goleski, J.A., Allam, B., Bowser, P., Tang, Y., and Nuzzi, R. 2008. Characterization, dynamics, and ecological impacts of harmful Cochlodinium polykrikoides blooms on eastern Long Island, NY, USA. Harmful Algae. 7:293-307.

Hoagland, P., Anderson, D.M., Kaoru, Y., and White, A.W. 2002. The economic effects of harmful algal blooms in the United States: estimates, assessment issues, and information needs. Estuaries and Coasts. 25(4):819-837.

Jeong, H.J., Kim, J.S., Yoo, Y.D., Kim, S.T., Song, J.Y., Kim, T.H., Seong, K.A., Kang, N.S., Kim, M.S., Kim, J.H., Kim, S., Ryu, J., Lee, H.M., and Yih, W.H. 2008. Control of the harmful alga Cochlodinium polykrikoides by the naked ciliate Strombidinopsis jeokjo in mesocosm enclosures. Harmful Algae. 7: 368-77.

Kim, D.W., Jo, Y.H., Choi, J.K., Choi, J.G., Bi, H. 2016. Physical processes leading to the development of an anomalously large Cochlodinium polykrikoides bloom in the East sea/Japan sea. Harmful Algae. 55: 250-258.

Lee, Y.S., Lee, S.Y. 2006. Factors affecting outbreaks of Cochlodinium polykrikoidesblooms in coastal areas of Korea. Marine Pollution Bulletin. 52, 5:626-634.

O’Neil, J.M., Davis, T.W., Burford, M.A., Gobler, C.J. 2012.The rise of harmful cyanobacteria blooms: The potential roles of eutrophication and climate change. Harmful Algae. 14:313-334.

Park, T.G., Lim, W.A., Park, Y.T., Lee, C.K., Jeong, H.J. 2013. Economic impact, management and mitigation  of red tides in Korea. Harmful Algae. 30, 1: 131-143.

Park, B.S., Kim, J.H., Kim, J.H., Gobler, C.J., Baek, S.H., Han, M.S. 2015. Dynamics of bacterial community structure during blooms of Cochlodinium polykrikoides (Gymnodiniales, Dinophyceae) in Korean coastal waters. Harmful Algae. 48: 44-54.

Rountos, K.J., Tang, Y.Z., Cerrato, R.M., Gobler, C.J., and Pikitch, E.K. 2014. Toxicity of the harmful dinoflagellate Cochlodinium polykrikoides to early life stages of three estuarine forage fish. Marine Ecology Progress Series. 505:81-94.

Tang, D.L., Kawamura, H., Doan-Nhu, H., Takahashi, W. 2004. Remote sensing oceanography of a harmful algal bloom off the coast of southeastern Vietnam. Journal of Geophysical Research.

Tang, Y.Z. and Gobler, C.J. 2008. Characterization of the toxicity of Cochlodinium polykrikoides isolates from Northeast US estuaries to finfish and shellfish. Harmful Algae. 8:454-462.

Tang, Y.Z. and Gobler, C.J. 2009. Cochlodinium polykrikoides blooms and clonal isolates from the northwest Atlantic coast cause rapid mortality in larvae of multiple bivalve species. Marine Biology. 156:2601-261