Benthic algae compensate for phytoplankton losses in large aquatic ecosystems

Anthropogenic activities can induce major trophic shifts in aquatic systems, yet we have an incomplete understanding of the implication of such shifts on ecosystem function and on primary production (PP) in particular. In recent decades, phytoplankton biomass and production in the Laurentian Great Lakes have declined in response to reduced nutrient concentrations and invasive mussels. However, the increases in water clarity associated with declines in phytoplankton may have positive effects on benthic PP at the ecosystem scale. Have these lakes experienced oligotrophication (a reduction of algal production), or simply a shift in autotrophic structure with no net decline in PP? Benthic contributions to ecosystem PP are rarely measured in large aquatic systems, but our calculations based on productivity rates from the Great Lakes indicate that a significant proportion (up to one half, in Lake Huron) of their whole-lake production may be benthic. The large declines (5–45%) in phytoplankton production in the Great Lakes from the 1970s to 2000s may be substantially compensated by benthic PP, which increased by up to 190%. Thus, the autotrophic productive capacity of large aquatic ecosystems may be relatively resilient to shifts in trophic status, due to a redirection of production to the near-shore benthic zone, and large lakes may exhibit shifts in autotrophic structure analogous to the regime shifts seen in shallow lakes

Comparison of techniques used to count single-celled viable phytoplankton

Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Journal of Applied Phycology 24 (2012): 751-758, doi:10.1007/s10811-011-9694-z.Four methods commonly used to count phytoplankton were evaluated based upon the precision of concentration estimates: Sedgewick Rafter and membrane filter direct counts, flow cytometry, and flow-based imaging cytometry (FlowCAM). Counting methods were all able to estimate the cell concentrations, categorize cells into size classes, and determine cell viability using fluorescent probes. These criteria are essential to determine whether discharged ballast water complies with international standards that limit the concentration of viable planktonic organisms based on size class. Samples containing unknown concentrations of live and UV-inactivated phytoflagellates (Tetraselmis impellucida) were formulated to have low concentrations (<100 ml-1) of viable phytoplankton. All count methods used chlorophyll a fluorescence to detect cells and SYTOX fluorescence to detect non-viable cells. With the exception of one sample, the methods generated live and non-viable cell counts that were significantly different from each other, although estimates were generally within 100% of the ensemble mean of all subsamples from all methods. Overall, percent coefficient of variation (CV) among sample replicates was lowest in membrane filtration sample replicates, and CVs for all four counting methods were usually lower than 30% (although instances of ~60% were observed). Since all four methods were generally appropriate for monitoring discharged ballast water, ancillary considerations (e.g., ease of analysis, sample processing rate, sample size, etc.) become critical factors for choosing the optimal phytoplankton counting method.This study was supported by the U.S. Coast Guard Research and Development Center under contract HSCG32-07- X-R00018. Partial research support to DMA and DMK was provided through NSF International Contract 03/06/394, and Environmental Protection Agency Grant RD-83382801-0

Grazing impacts of the invasive bivalve Limnoperna fortunei (Dunker, 1857) on single-celled, colonial and filamentous cyanobacteria

Feeding behavior of the invasive bivalve Limnoperna fortunei in the presence of single-celled, colonial, and filamentous cyanobacteria was tested in laboratory experiments to evaluate the effects of size and shape on mussel feeding. The first hypothesis holds that golden mussel filters more efficiently smaller particles, such as single cells of Microcystis, which could be more easily assimilated by its filtering apparatus. The second hypothesis sustains that L. fortunei filters more efficiently rounded colonies, such as Microcystis, which would be more easily ingested than lengthy filamentous, such as Planktothrix. Filtration rates of golden mussel in the presence of single-celled, colonial and filamentous cyanobacteria were similar. Nevertheless, there was a great difference in the ingestion and pseudofeces production rates. Single cells were widely accepted as food, while filamentous and colonial cyanobacteria were massively expelled as pseudofeces. The results confirmed the first hypothesis that golden mussel prefers to ingest smaller particles. The second hypothesis was rejected since filamentous were preferentially ingested than colonial cyanobacteria. Golden mussel has the potential to remove toxic cells (Microcystis), however this potential would be reduced in cyanobacteria blooms, where colonial forms which are preferentially rejected by L. fortunei, are predominant. In this case, the presence of this invasive bivalve could also enhance the occurrence of blooms by rejecting colonial and filamentous cyanobacteria in pseudofeces