Known as Golden Algae in popular media, Prymnesium parvum causes harmful algal blooms. When stressed, it secretes increased amounts of toxic chemicals called prymnesins, which have resulted in major fish kills in Texas. Although many options exist for mitigation of blooms, a feasible protocol for control of blooms on large-scale impoundments has yet to be identified. Chemical control of P. parvum using six different enzyme inhibiting aquatic herbicides was explored in laboratory experiments. Of the six chemicals screened, one (Flumioxazin) was selected for further study due to a significant decrease in P. parvum cell numbers with increasing chemical concentration. It was applied to natural plankton communities during in-situ experiments (Lake Granbury, Texas). The first experiment was conducted during a period of P. parvum bloom initiation (March) and the second experiment conducted during a post bloom period (April). Experiments were carried out in 20 L polycarbonate carboys covered in 30% shade cloth to simulate natural light, temperature and turbulence conditions. Flumioxazin was additionally screened in the laboratory on the common game/forage fish bluegill sunfish (Lepomis macrochirus) for six weeks with weekly re-application of flumioxazin to treatment tanks. Cell counts via light-microscopy, showed the chemical flumioxazin caused significant decreases in P. parvum, but no significant differences in zooplankton abundance during the period of bloom initiation. However, significant decreases in adult copepods were observed during the post bloom period, most likely due to decreased light penetration and inhibition of the photosensitive mode of action, but no significant decreases in P. parvum. No significant effects of flumioxazin were observed on growth, survival or feed conversion ratio for L. macrochirus.

Pyrmnesium parvum, commonly known as golden algae, is an algal species that under certain circumstances releases toxins which can lead to fish kills and the death of other economically and ecologically important organisms. One of the major objectives of the study was to investigate whether a relationship exists between land use and Prymnesium parvum abundance in littoral sites of Lake Texoma, USA. Another objective was to investigate whether a relationship exists between other physical variables and counts of P. parvum. Lastly, developing a valid model that predicts P. parvum abundance was an objective of the study. Through stepwise regression, a small but highly significant amount of the variation in P. parvum counts was found to be explained by wetlands, soil erodibility and lake elevation. The developed model provides insight for potential golden algae management plans, such as maintaining wetlands and teaching land owners the relationship between soil erosivity and golden algae blooms.

Prymnesium parvum Carter, a haptophyte species capable of forming harmful algal blooms (HABs), has been identified in fresh and brackish water habitats worldwide. In Texas, P. parvum blooms have diminished local community revenues from losses to tourism, fishing, and hatchery production. In this thesis, P. parvum dynamics were studied using in-situ microcosm experiments at Lake Possum Kingdom, Texas during three seasons (fall, winter, spring) in 2004-2005. Specifically, nutrient additions were used to test the hypothesis that increased nutrient levels would not enhance P. parvum's ability to invade phytoplankton communities. In addition to full nutrient additions to levels of f/2 media, other treatments included nutrient additions deficient in either nitrogen (N) or phosphorus (P). Additionally, barley straw extract was tested as a growth inhibitor to prevent P. parvum blooms. Furthermore, P. parvum initial population density was examined to test the hypothesis that increased initial populations could promote an increase in P. parvum population densities. Findings indicated that P. parvum populations in Lake Possum Kingdom would not likely gain a selective advantage over other species when inorganic nutrients (nitrogen and phosphorus) were not limiting. P. parvum did, however, gain an advantage during both N- and P-limited conditions as indicated by toxicity, cell concentrations, and bulk phytoplankton community shifts. Furthermore, P. parvum blooms in Lake Possum Kingdom would likely not be inhibited by barley straw extract application. Initial population densities affected the final population density, but only when initial populations were low. A method to quickly and accurately detect the presence of P. parvum is needed due to P. parvum's potential to cause toxic and lethal blooms. This thesis tested whether P. parvum photopigments are conservative regardless of growth conditions and could be used to quantify the relative abundance of P. parvum in mixed community samples. If biomarker pigments are conservative, then an optimized version of CHEMTAX could be employed as an alternative diagnostic tool to microscopy for enumeration of P. parvum. However, P. parvum pigments in the Texas strain were not conservative throughout the growth cycle and therefore may not be a reliable indicator of cell abundance.

Prymnesium parvum Carter, a haptophyte species capable of forming harmful algal blooms (HABs), has been identified in fresh and brackish water habitats worldwide. In Texas, P. parvum blooms have diminished local community revenues from losses to tourism, fishing, and hatchery production. In this thesis, P. parvum dynamics were studied using in-situ microcosm experiments at Lake Possum Kingdom, Texas during three seasons (fall, winter, spring) in 2004-2005. Specifically, nutrient additions were used to test the hypothesis that increased nutrient levels would not enhance P. parvum's ability to invade phytoplankton communities. In addition to full nutrient additions to levels of f/2 media, other treatments included nutrient additions deficient in either nitrogen (N) or phosphorus (P). Additionally, barley straw extract was tested as a growth inhibitor to prevent P. parvum blooms. Furthermore, P. parvum initial population density was examined to test the hypothesis that increased initial populations could promote an increase in P. parvum population densities. Findings indicated that P. parvum populations in Lake Possum Kingdom would not likely gain a selective advantage over other species when inorganic nutrients (nitrogen and phosphorus) were not limiting. P. parvum did, however, gain an advantage during both N- and P-limited conditions as indicated by toxicity, cell concentrations, and bulk phytoplankton community shifts. Furthermore, P. parvum blooms in Lake Possum Kingdom would likely not be inhibited by barley straw extract application. Initial population densities affected the final population density, but only when initial populations were low. A method to quickly and accurately detect the presence of P. parvum is needed due to P. parvum's potential to cause toxic and lethal blooms. This thesis tested whether P. parvum photopigments are conservative regardless of growth conditions and could be used to quantify the relative abundance of P. parvum in mixed community samples. If biomarker pigments are conservative, then an optimized version of CHEMTAX could be employed as an alternative diagnostic tool to microscopy for enumeration of P. parvum. However, P. parvum pigments in the Texas strain were not conservative throughout the growth cycle and therefore may not be a reliable indicator of cell abundance.

Inflows affect water quality, food web dynamics, and even the incidence of harmful algal blooms. It may be that inflows can be manipulated to create refuge habitat for biota trying to escape poor environmental conditions, such as fish populations in lakes during times of toxic Prymnesium parvum blooms. Water availability sometimes can be an issue, especially in arid climates, which limits this approach to management. Utilizing source water from deeper depths to displace surface waters, however, might effectively mimic inflow events. I test this notion by conducting in-lake mesocosm experiments with natural plankton communities where I manipulate hydraulic flushing. Results show that P. parvum cell density is reduced by 69%, and ambient toxicity completely ameliorates during pre-bloom conditions in the lake. During conditions of bloom development, population density is reduced by 53%, toxicity by 57%, and bloom proportions are never reached. There is minimal effect of these inflows on total phytoplankton and zooplankton biomass, and little effect on water quality. Shifts toward more rapidly growing phytoplankton taxa are observed, as are enhanced copepod nauplii. In other words, while inflows using deep waters suppress P. parvum bloom initiation and development, they are benign to other aspects of the lower food web and environment. The results from using deep lake water to suppress harmful algal blooms indicate this may be a promising management approach and further studies are recommended to test whether this mitigating effect can translate to a large-scale in-lake treatment.

This dissertation includes molecular and phytochemical investigations of the harmful, bloom-forming alga, Prymnesium parvum, including analysis of known polyketide metabolites as a function of salinity and growth. Initially, the development of molecular and phytochemical tools was necessary for the detection and quantification of P. parvum and its associated toxins. Suites of oligonucleotides and molecular beacons were designed for conventional and quantitative multiplex PCR to amplify four species- and gene-specific products simultaneously that were used for the detection and quantitation of P. parvum. This built-in redundancy provided increased confidence in reactions with the positive confirmation of four discrete products. Techniques were also developed for the chemical enrichment of toxins produced by P. parvum. Until now, isolation of “prymnesins” has never been reproduced. Polyketide prymnesins possess unique spectral properties that were used to generate an LC-MS fingerprint that comprised 13 ion species. Preliminary investigations using chemifluorimetric methods were also capable of detecting prymnesins in the pico- and nano-molar range. Environmental samples were tested as an independent assessment of these methods. Lastly, the roles of polyketide prymnesins were analyzed with respect to total hemolytic activity (HA) as a function of culture age and salinity. Variation in HA of supernatants was statistically significant relative to both variables (p << 0.05). Salinity was inversely related to HA wherein cultures growing in 5-25 psu were 150-200% more hemolytic. Total HA was inversely related to culture age during the first three weeks, but positively related to it during the next three weeks. Interestingly, no hemolysis was detected in fractions containing prymnesins from culture supernatants and the majority of hemolysins remained in the aqueous phase. Prymnesins extracted from cells varied significantly over the 6-week observation period (p << 0.05); HA was positively correlated during the first half and inversely related during the last half of the study. Salinity was directly related to HA from cell extracts, but these effects were not significantly different until the last three weeks. These investigations suggest that polyketide prymnesins are present at much lower quantities than previously believed, and they may not be the key compounds associated with hemolysis due to P. parvum. / text

Phytoplankton produce allelochemicals; excreted chemical substances that are affecting other microorganisms in their direct environment. In my thesis, I investigated strain specific variability in the expression of allelochemicals of the harmful flagellate Prymnesium parvum, that is euryhaline but mainly bloom forming in brackish water. I found a large variation among strains, but further showed that all strains of P. parvum were more allelopathic in brackish water compared to marine water. In a marine microbial community, allelochemicals can affect prey, competitors and grazers both, directly and indirectly. For instance, in a food web where grazing controls prey abundance, the negative direct effect of allelochemicals on grazers will positive affect their prey. During my thesis, I investigated how marine microbial communities respond to the addition of allelochemicals. I performed field experiments with microbial communities from seawater collected from different places over Europe, and tested how this communities respond to the addition of allelochemicals from the dinoflagellate Alexandrium tamarense. Before I incubated the microbial communities for several days with A. tamarense algal filtrate, I evaluated the allelopathic efficiency of the algal filtrates with an algal monoculture of Rhodomonas spp. This allowed me to compare the effect of A. tamarense filtrate between the different microbial communities. In general, bacteria reached higher abundances when allelochemicals were present. As allelochemicals also inhibited nanoflagellates and ciliates, we concluded, that allelochemicals indirectly benefit bacteria by reducing grazing pressure. In microbial food webs with many heterotrophic grazers, allelochemicals further benefitted other phytoplankton by inhibiting grazers. It was also shown that bioavailable DOM is released from a microbial community when allelochemicals are present. As most DOM was released from the seawater fraction &gt; 60 μm, we concluded, that larger microorganisms are more affected by allelochemicals than smaller microorganisms. The results can be explained by the surface to volume ratio of microorganisms: Larger organisms provide more contact surface for allelochemicals, and therefore, are probably more vulnerable towards allelochemicals. In conclusion, the effect of allelochemicals on a microbial community depends among others on the structure of the microbial food web, the amount of available DOM, the particle density in the seawater and the composition of the phytoplankton community.

Thesis (M.S.)--Baylor University, 2008. / Includes bibliographical references (p. 68-74)

Thesis (M.S.)--University of North Carolina at Wilmington, 2005. / Includes bibliographical references (leaves: [70]-74)