Throughout the United States, many eutrophic freshwater bodies experience seasonal blooms of toxic cyanobacteria. These blooms limit recreational uses and pose a threat to both human and ecological health. Traditional bi-weekly chlorophyll-based sampling programs designed to assess overall algal biomass fail to capture important bloom parameters such as bloom timing, duration, and peak intensity. In-situ optical and fluorometric measurements have the potential to fill this gap. However, relating in-situ measurements to relevant water quality measures (e.g. cyanobacterial cell density or chlorophyll concentration) is a challenge that limits the implementation of probe-based monitoring strategies. This study, of Aphanizomenon dominated blooms in Boston's Charles River, combines five years of cyanobacterial cell counts with high resolution insitu sensor measurements to relate turbidity and fluorometric readings to cyanobacterial cell density. Our work compares probe and lab-based estimates of summer-mean chlorophyll concentration and highlights the challenges of working with raw fluorescence in cyanobacteria dominated waterbodies. A strong correlation between turbidity and cyanobacterial cell density (R 2 = 0.84) is used to construct a simple cell-density-estimation-model suitable for triggering rapid bloom-responsesampling and classifying bloom events with a true positive rate of 95%. The approach described in this study is potentially applicable to many cyanobacteria dominated freshwater bodies.
Keywords: Chlorophyll; Cyanobacteria; Harmful algal bloom; Phycocyanin; Real-time monitoring; Turbidity.
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