Microcystis Cells Research Articles

Mini-Hydrocyclone Separation of Cyanobacterial and Green Algae: Impact on Cell Viability and Chlorine Consumption

The co-occurrence of non-toxic phytoplankton alongside cyanobacteria adds to the challenge of treating source waters with harmful algal blooms. The non-toxic species consume the oxidant and, thereby, reduce the efficacy of oxidation of both the extracellular and intracellular cyanotoxins. In this work, a 3D printed mini-hydrocyclone was used to separate a mixture of non-toxic green algae, Scenedesmus obliquus, from a toxic species of cyanobacteria, Microcystis aeruginosa. When water is pumped through the mini-hydrocyclone, cells exit through an overflow or underflow port depending on their size, shape, and density relative to the other cells and particles in the water matrix. The overflow port contains the cells that are smaller and less dense since these particles move toward the center of the hydrocyclone. In this work, the majority (>93%) of Microcystis cells were found in the overflow while the underflow contained primarily the Scenedesmus (>80%). This level of separation efficiency was maintained over the 30-min experiment and the majority of both cells (>86%) remained viable following the separation, which indicates that the pumping combined with forces exerted within the mini-hydrocyclone were not sufficient to cause cell death. The impact of free chlorine on the cells both pre-separation and post-separation was evaluated at two doses (1 and 2 mg/L). After separation, the overflow, which contained primarily Microcystis, had at least a 24% reduction in the free chlorine decay rate as compared to the feed water, which contained both species. This reduction in chlorine consumption shows that the cells separated via mini-hydrocyclone would likely require lower doses of oxidant to produce a similar level of degradation of the cyanotoxins present in either the extracellular or intracellular form. However, future work should be undertaken to evaluate this effect in natural bloom samples.

Phosphorus strategy in bloom-forming cyanobacteria (Dolichospermum and Microcystis) and its role in their succession

Dolichospermum (formerly Anabaena) and Microcystis cause harmful cyanobacterial blooms in freshwater ecosystems worldwide. Input reduction of both nitrogen (N) and phosphorus (P) are commonly recognized as basic ways of controlling blooms, but little is known about the roles of nutrients and their using strategy among cyanobacteria in triggering the succession of diazotrophic to non-diazotrophic cyanobacteria. In this study, we investigated in situ responses of cyanobactria to ambient P status during the transition from Dolichospermum flos-aquae to Microcystis spp. in Lake Taihu and Lake Chaohu. While dominant in phytoplankton community, D. flos-aquae experienced P deficiency as evidenced by qualitative detection of extracellular phosphatase via enzyme labeled fluorescence (ELF). The percentage of ELF-labelled D. flos-aquae cells was 33% when it dominated the phytoplankton community, and was 78% when it co-dominated with Microcystis spp., indicating an increase in P deficiency. Meanwhile, no ELF-labelled Microcystis cells were observed while polyphosphate body (PPB) were present, suggesting that Microcystis spp. were not P deficient. Additionally, the percentages of Microcystis cells containing PPB showed an inverted “U-shaped” relationship with concentrations on soluble reactive phosphorus (SRP). To validate the field observation, a laboratory study of the monocultures of the dominant cyanobacteria was conducted. Extracellular alkaline phosphatase activity (APA) and PPB accumulation were regulated by P availability in monocultures of D. flos-aquae. Interestingly, no cell bound extracellular phosphatase was found on Microcystis aeruginasa even in the culture without P supply. Consistently, the expressions of phosphatase encoding gene phoX showed no differences among the treatments. The way in which PPB accumulation occurred in Microcystis spp. in response to P availability in the cultures was similar to that observed in the field, demonstrating a strategy of energy conservation over P accumulation. The competitive advantage of Microcystis spp. was displayed at low P concentrations: where it could rapidly uptake and store inorganic P, which also increased the P deficiency of the coexisting phytoplankton species. Responses of P-transport gene pstS confirmed this hypothesis. The physiological and molecular mechanisms mentioned above enable Microcystis to survive and proliferate in environment with low available P supply more efficiently. In conclusion, different cyanobacterial species have distinct ways of responding to P availability, suggesting that the control of cyanobacterial blooms by targeted nutrient reduction is largely dependent upon the dominant species. P reduction is more effective in controlling diazotrophic cyanobacteria than non-diazotrophic cyanobacteria.

Removal of Microcystis blooms using enhanced colony formation and buoyancy by controlling extracellular polysaccharides and cation concentrations

This study attempted to promote the colony formation and enlarge the colony size of wild Microcystis strain by adjusting extracellular polysaccharides and cationic ion concentrations in culture medium, and then, using the enhanced floating velocity (Stokes’ law), wild Microcystis at the water surface was removed. In order to examine the difference between extracellular polysaccharides mixture and tightly cell-bound extracellular polysaccharides used in this study, the component composition and physical properties were also examined. The results showed that tightly cell-bound extracellular polysaccharides contained the greater amounts of cations (Ca2+ and Mg2+), phosphorus, carboxy group and monosaccharides than extracellular polysaccharides mixture. There were greater amounts of carboxy groups and mannose residue in tightly cell-bound extracellular polysaccharides than extracellular polysaccharides mixture, which would contribute to the stronger cell–cell adhesion of wild Microcystis to make colony formation and expand colony size. The adjustment of extracellular polysaccharides and cationic ion concentrations was effective method to promote the colony formation and enlarge the colony size of wild Microcystis, and that the control of Microcystis buoyancy by enhancing the colony size would be one of the options for the suppression of Microcystis blooms from the viewpoint of cost-effective, low-energy, environmentally-friendly, and non-destructive of Microcystis cells.

The Individual and Combined Effects of the Cyanotoxins, Anatoxin-a and Microcystin-LR, on the Growth, Toxin Production, and Nitrogen Fixation of Prokaryotic and Eukaryotic Algae.

Globally, eutrophication and warming of aquatic ecosystems has increased the frequency and intensity of cyanobacterial blooms and their associated toxins, with the simultaneous detection of multiple cyanotoxins often occurring. Despite the co-occurrence of cyanotoxins such as microcystins and anatoxin-a (ATX) in water bodies, their effects on phytoplankton communities are poorly understood. The individual and combined effects of microcystin-LR (MC-LR) and ATX on the cyanobacteria Microcystis spp., and Anabaena variabilis (a.k.a. Trichormus variabilis), and the chlorophyte, Selenastrum capricornutum were investigated in the present study. Cell density, chlorophyll-a content, and the maximum quantum efficiency of photosystem II (Fv/Fm) of Microcystis cells were generally lowered after exposure to ATX or MC-LR, while the combined treatment with MC-LR and ATX synergistically reduced the chlorophyll-a concentration of Microcystis strain LE-3. Intracellular levels of microcystin in Microcystis LE-3 significantly increased following exposure to MC-LR + ATX. The maximum quantum efficiency of photosystem II of Anabaena strain UTEX B377 declined during exposure to the cyanotoxins. Nitrogen fixation by Anabaena UTEX B377 was significantly inhibited by exposure to ATX, but was unaffected by MC-LR. In contrast, the combination of both cyanotoxins (MC-LR + ATX) caused a synergistic increase in the growth of S. capricornutum. While the toxins caused an increase in the activity of enzymes that scavenge reactive oxygen species in cyanobacteria, enzyme activity was unchanged or decreased in S. capricornutum. Collectively this study demonstrates that MC-LR and ATX can selectively promote and inhibit the growth and performance of green algae and cyanobacteria, respectively, and that the combined effect of these cyanotoxins was often more intense than their individual effects on some strains. This suggests that the release of multiple cyanotoxins in aquatic ecosystems, following the collapse of blooms, may influence the succession of plankton communities.

Sono-Fenton hybrid process on the inactivation of Microcystis aeruginosa: Extracellular and intracellular oxidation

For the first time, the inactivation of Microcystis aeruginosa using sono-Fenton process at low frequency high intensity (20 kHz, 0.42 W/mL) and high frequency low intensity (800 kHz, 0.07 W/mL) was investigated, respectively. 20 kHz sono-Fenton treatment successfully reduced cyanobacterial cell number from 4.19 × 106 cells/mL to 0.45 × 106 cells/mL within 5 min treatment. Alternatively, efficient performance of 800 kHz sono-Fenton process was observed to decrease Microcystis cell number to 2.33 × 106 cells/mL after 5 min inactivation, with lower energy cost. It was found that powerful 20 kHz sonication induced pore formation on the cell wall, leading to extracellular damage, while 800 kHz irradiation with low intensity triggered intracellular uptake of chemicals, suggesting endocytosis effects. Furthermore, sono-Fenton Processes were found to be affected by the concentrations of Fenton’s reagent, and pre-sonication time. Although solo Fenton treatment released microcystins in water, the degradation of microcystin-LR were achieved using 20 and 800 kHz sono-Fenton processes, respectively. The results of this work showed that severe extracellular oxidation is the vital inactivation mechanism of 20 kHz sono-Fenton process, while the internal oxidation caused by intracellularly delivered Fenton reagents is suggested to be the main cause of 800 kHz sono-Fenton inactivation, leading to much lower energy cost. This work provides alternative methods to control harmful cyanobacteria in water towards effective treatment.

Variation and diversity of genus microcystis in the water environment of the Nui Coc reservoir, Thai Nguyen province

The Nui Coc reservoir, Thai Nguyen province was built on the Cong River for multi-purposes of providing water for local people such as agricultural irrigation, aquaculture, tourism activities and especially the drinking water supply for the Thai Nguyen city and other surrounding areas. This paper presents the results of the monthly surveys which were conducted during the year 2011 for determination of diversity of Microcytis and the microcystin contents in the isolated Microcystis strains in the water environment of the Nui Coc reservoir. The present results showed that eight species of Microcytis genus of which Microcystis aeruginosa in the water environment of the Nui Coc reservoir was the most abudance. The Microcystis cell density of the Nui Coc reservoir varied seasonally and the highest values were observed in high temperature in the rainy season. The results from the High-Performance Liquid Chromatography (HPLC) analysis showed that the microcystin contents in the isolated Microcystis strains from the Nui Coc reservoir ranged from 0.116 to 0.40 µg MC/mg dried mass. The high cell density of Microcystis and high microcystin concentrations in the isolated Microcystis strains from the Nui Coc reservoir revealed the potential risk for human health. The results also highlighted that it is very necessary and urgent to carry out regular monitoring programs for detecting the occurrence of cyanobacteria and phytoplankton in the water environment of the Nui Coc reservoir in order to timely warn the potential risk of cyanobacteria boom and the adverse impacts on the aquatic ecosystem and especially on human health.

Establishing spatial and temporal patterns in Microcystis sediment seed stock viability and their relationship to subsequent bloom development in Western Lake Erie.

This study assessed the distribution, abundance, and viability of pre- and post-overwintering Microcystis sediment seed stocks in Western Lake Erie and how these variables are potentially related to past and subsequent bloom formation. We conducted a two-year spatiotemporal survey of vegetative seed stocks in Western Lake Erie, the region where annual algal blooms generally develop. Sediment was collected from 16 sites covering an area of 375 km2 and water column depths ranging from 3–9 meters. Sample collection occurred in November 2014, April 2015, November 2015, and April 2016. The abundance of total and potentially-toxic Microcystis cell equivalents were determined using quantitative polymerase chain reaction. A series of laboratory experiments using lake sediment were conducted to assess the viability of Microcystis vegetative seed stocks. Across all sampling periods, the abundance of total Microcystis in the sediment ranged from 6.6 x 104 to 1.7 x 109 cell equivalents g-1, and potentially-toxic Microcystis ranged from 1.4 x 103 to 4.7 x 106 cell equivalents g-1. The percent potentially-toxic Microcystis in the sediment ranged from <1% to 68% across all samples. Total Microcystis abundance diminished significantly over winter with densities in spring nearly 10 times less than the previous fall. However, despite cell loss from fall to spring, lab experiments demonstrated that remaining non-toxic and potentially-toxic cells were viable after the overwintering period. Further, lab grow-out experiments indicate that potentially-toxic strains recruited at a slightly higher rate than non-toxic strains, and may in part, contribute to the pattern of higher relative toxicity during early stages of the blooms. The abundance and distribution of overwintering cells did not correlate strongly to areas in the lake where subsequent summer blooms were most persistent. However, numerical analysis suggests that recruitment of benthic overwintering populations could help explain a portion of the initial rapid increase in bloom biomass and the spatial extent of this bloom initiation, particularly when recruitment is paired with subsequent growth in appropriate water column conditions.

Influences of small-scale oscillations on growth inhibition and ultrastructural changes of Microcystis cells

We investigated the effects of small-scale oscillation (SSO) on toxic Microcystis cells. The oscillating device was made of silicon with two axes that had a diameter of ∼40 mm, and a frequency of 2.5 Hz was observed at 150 rpm. The SSO was effective in inhibiting Microcystis growth. Microcystin release was not observed, whereas cell density barely increased in the oscillating group. Cell size and morphology of the oscillating group were no different from the control group. However, cell quotas of chl.a and microcystin in the oscillating group were half the level of the control group. Crucially, a number of large-sized holes were observed and layered long linear thylakoids were rarely observed in the oscillating group. Therefore, SSO was found to be very effective in Microcystis growth inhibition, and it caused ultrastructural changes without damage to the cell membrane and subsequent microcystin release.

Grazing of the copepod Cyclops vicinus on toxic Microcystis aeruginosa: potential for controlling cyanobacterial blooms and transfer of toxins

Abstract Grazing of zooplankton on phytoplankton may contribute to a reduction of harmful cyanobacteria in eutrophic waters. However, the feeding capacity and interaction between zooplankton and toxic cyanobacteria vary among grazer species. In this study, laboratory feeding experiments were designed to measure the grazing rate of the copepod Cyclops vicinus on Microcystis aeruginosa and the potential microcystin (MC) accumulation in the grazer. Copepods were fed a mixed diet of the edible green alga Ankistrodesmus falcatus and toxic M. aeruginosa for 10 days. The results showed that C. vicinus efficiently ingested toxic Microcystis cells with high grazing rates, varying during the feeding period (68.9–606.3 Microcystis cells animal-1 d-1) along with Microcystis cell density. Microcystis cells exhibited a remarkable induction in MC production under grazing conditions with concentrations 1.67–12.5 times higher than those in control cultures. Furthermore, C. vicinus was found to accumulate MCs in its body with concentrations increasing during the experiment (0.05–3.21 μg MC animal-1). Further in situ studies are needed to investigate the ability of Cyclops and other copepods to assimilate and detoxify MCs at environmentally relevant concentrations before deciding on the biocontrol of Microcystis blooms by copepods.

Autoaggregation and adhesion abilities in bacteria associated with colonies of Microcystis

Bacteria associated with Microcystis may play an important role in formation of Microcystis colonies and in development of cyanobacterial blooms. Adhesion to Microcystis cells is a requirement for colonization and long-term association of bacteria with Microcystis colonies. This study aimed to explore the relationship between autoaggregation ability and adhesion ability of Microcystis-associated bacteria, and to evaluate the effects of different environmental factors on their autoaggregation abilities. Twelve bacterial strains were isolated from colonies of three Microcystis morphospecies. All the bacterial isolates exhibited autoaggregation abilities. A positive correlation was found between autoaggregation ability and adhesion ability. Two selected bacterial isolates, HJX5 and HJX9, exhibited strong autoaggregation abilities at pH from 3 to 11. The laboratory experiment revealed the inhibitory effects of metal cations on the autoaggregation abilities of HJX5 and HJX9, but HJX5 and HJX9 could exhibit their autoaggregation abilities in the lake water. Extraction of exopolysaccharides (EPS) decreased significantly their autoaggregation abilities, indicating that EPS can play an important role in autoaggregation. The autoaggregation ability of Microcystis-associated bacteria may be an important trait contributing to their attachment into Microcystis colonies.

Recruitment-promoting of dormant Microcystis aeruginosa by three benthic bacterial species

The frequent occurrence of Microcystis aeruginosa blooms benefit from the dormant Microcystis cells, which will be recruited from sediment into overlying water to form a dominant population and algal blooms when external environmental conditions are suitable. Previous studies have unveiled factors involved in M. aeruginosa recruitment and bloom initiation, including nutrition, illumination, temperature, and hydrodynamic force. In this study, three dominant benthic bacterial species isolated from Lake Chongtian with frequent blooms-forming were identified through next generation sequencing (NGS) techniques, and laboratory experiments were conducted on the recruitment of dormant M. aeruginosa cells via co-culture with these bacteria at 10 °C, 15 °C, 20 °C and 25 °C. The results showed that the bacterial strains in sediment proliferated quickly before recruitment of dormant M. aeruginosa cells, subsequently significantly promoted the recruitment of dormant M. aeruginosa via allelochemical (metabolite) production, lower N:P values and lower dissolved oxygen concentrations in the sediment-water interface, and enhanced photosynthesis of M. aeruginosa cells. Furthermore, dormant M. aeruginosa was recruited from sediment at 10 °C when bacterial activity was present, but not recruited when bacterial activity was absent. At 15 °C,20 °Cand 25 °C, there were no remarkable differences in the recruitment rate of dormant M. aeruginosa cells among all bacterial groups, although their recruitment rate were significantly higher than that at 10 °C.These findings suggested that, under laboratory conditions, three benthic bacteria not only had a great influence on promoting the recruitment of dormant M. aeruginosa cells under desirable temperatures, but also can spur recruitment of dormant M. aeruginosacells from sediment at lower temperature (10 °C).

Involvement of microcystins, colony size and photosynthetic activity in the benthic recruitment of Microcystis

Cyanobacterial blooms in aquatic environments are a worldwide problem that greatly depend on the recruitment of benthic Microcystis species. In addition to environmental factors, physiological characteristics are also crucial for benthic recruitment of Microcystis, although the exact details remain poorly understood. In the present study, we studied the involvement of physiological characteristics in benthic recruitment from three aspects: photosynthetic activity, colony size and intracellular microcystin (MC) content. After UV irradiation the Microcystis cells were damaged and in poor physiological state. Normal benthic Microcystis (NBM) exhibited higher recruitment than damaged benthic Microcystis (DBM). This might be explained by the difference in photosynthetic activity. Small benthic colonies (20–60 μm) could reinvade the water column from sediments more easily than large colonies. Furthermore, poor physiological state was correlated with lower survival of large colonies (140–220 μm) which might decompose into smaller colonies (40–80 μm). Toxic Microcystis not only survived more easily than non-toxic ones in sediments but also recruited more readily into the water column from sediments. This might be due to the presence of intracellular MCs. During the benthic phase, toxic Microcystis might consume or release intracellular MCs to acclimate to benthic environment. We also found that sediment mixing in the form of passive suspension facilitated recruitment, but physiological characteristics, an active process, played a more decisive role. This knowledge on the physiological characteristics of Microcystis expands our understanding of benthic recruitment.

Exposure of Microcystis aeruginosa to hydrogen peroxide and titanium dioxide under visible light conditions: Modeling the impact of hydrogen peroxide and hydroxyl radical on cell rupture and microcystin degradation

The aims of this study are to evaluate, under visible light conditions, the ability of H2O2 and TiO2 to produce OH, their quantitative impacts on the cell integrity of Microcystis, and the subsequent release and degradation of microcystins (MCs). A sequential reaction model was developed, including one sub-model to simulate the rupture kinetics for cell integrity of Microcystis, and another to describe the release and degradation of MCs. For cell rupture, the dual-oxidant Delayed Chick-Watson model (DCWM) and dual-oxidant Hom model (HM) were first proposed and developed, giving excellent simulation results of cell rupture kinetics. Kinetic rate constants between Microcystis cells and H2O2(kH2O2, Cell) as well as OH (k•OH, Cell) under visible light successfully separated the individual effects of H2O2 and OH on Microcystis. The dual-oxidant models were further validated with additional experiments, making the models more convincing. Finally, the dual-oxidant cell rupture models were integrated with the MC degradation model and well predicted the observed MCs concentrations in the experimental systems. The results of this study not only demonstrate the potential application of H2O2 and TiO2 for the control of cyanobacteria and metabolites in natural water bodies, but also provide a new methodology to differentiate the individual contributions of the two oxidants, H2O2 and OH, on cell rupture, thus giving a novel way to more precisely determine the effective doses of applied oxidants for cyanobacteria control.

Analysis of cyanobacterial metabolites in surface and raw drinking waters reveals more than microcystin

Freshwater cyanobacterial blooms are becoming increasingly problematic in regions that rely on surface waters for drinking water production. Microcystins (MCs) are toxic peptides produced by multiple cyanobacterial genera with a global occurrence. Cyanobacteria also produce a variety of other toxic and/or otherwise bioactive peptides (TBPs) that have gained less attention including cyanopeptolins (Cpts), anabaenopeptins (Apts), and microginins (Mgn). In this study, we compared temporal and spatial trends of four MCs (MCLR, MCRR, MCYR, MCLA), three Cpts (Cpt1020, Cpt1041, Cpt1007), two Apts (AptF, AptB), and Mgn690 in raw drinking water and at six surface water locations above these drinking water intakes in a eutrophic lake. All four MC congeners and five of six TBPs were detected in lake and raw drinking water. Across all samples, MCLR was the most frequently detected metabolite (100% of samples) followed by MCRR (97%) > Cpt1007 (74%) > MCYR (69%) > AptF (67%) > MCLA (61%) > AptB (54%) > Mgn690 (29%) and Cpt1041 (15%). Mean concentrations of MCs, Apts, and Cpts into two drinking water intakes were 3.9 ± 4.7, 0.14 ± 0.21, and 0.38 ± 0.92, respectively. Mean concentrations in surface water were significantly higher (p < 0.05) than in drinking water intakes for MCs but not for Cpts and Apts. Temporal trends in MCs, Cpts, and Apts in the two raw drinking water intakes were significantly correlated (p < 0.05) with measures of cell abundance (chlorophyll-a, Microcystis cell density), UV absorbance, and turbidity in surface water. This study expands current information about cyanobacterial TBPs that occur in lakes and that enter drinking water treatment plants and underscores the need to determine the fate of less studied cyanobacterial metabolites during drinking water treatment that may exacerbate toxicity of more well-known cyanobacterial toxins.

Degradation of lincomycin in aqueous solution with hydrothermal treatment: Kinetics, pathway, and toxicity evaluation

Recently, lincomycin has been detected frequently in aquatic environment, especially in the effluent of pharmaceutical wastewater treatment plants. Public concerns have been raised due to its adverse bio-effect and potential of inducing resistance genes. In this study, hydrothermal treatment (HT) was applied to remove lincomycin from high-concentrated pharmaceutical waste water. Influence factors (e.g., temperature, initial concentration and pH) were investigated from kinetics perspective. Meanwhile, degradation byproducts were identified using liquid chromatography–mass spectrometry (LC–MS), based on that transformation pathways were proposed. Finally, the toxicity of lincomycin degradation intermediates were evaluated by Microcystis cells. The results showed that lincomycin was eliminated efficiently via HT and an obvious lag time existed in its degradation process. An autocatalytic model was developed successfully based on the degradation kinetics analysis. The model showed good fitness with experiments data (R2 > 0.99). Observed reaction constant (k) increased when reaction temperature varied from 110 to 160 °C; it decreased from 0.034 to 0.015 min−1 as pH ranged from 2.0 to 6.0. Additionally, increasing initial concentration of lincomycin promoted its degradation, while it showed a different trend once the concentration exceeded 300 mg L−1. A total of 7 major intermediates were identified, based on which hydrolysis, hydroxylation and desulfuration were inferred as the mainly evolution processes. Finally, toxicity evaluation indicated that both lincomycin and its degradation byproducts have no inhibition on algal strains. Thus, it is concluded that HT is an efficient method for removing lincomycin.

Establishment of a new strategy against Microcystis bloom using newly isolated lytic and toxin-degrading bacteria

Unwanted, rapid increases in the algal populations of water systems cause harmful algal blooms, which have recently become a major environmental problem. The cyanobacterium Microcystis aeruginosa is the most prevalent bloom species and is responsible for the majority of blooms in freshwater environments. In this study, we attempted to develop an eco-friendly method to suppress M. aeruginosa bloom based on a biological control using bacteria newly isolated from the soil. In a screen for bacteria with strong lethal activity toward Microcystis, we isolated Bacillus sp. T4 and characterised its algicidal activity. Microcystis aeruginosa cells were killed via indirect attack by compound(s) secreted by T4 bacteria. ELISA revealed a dramatic increase in extracellular microcystins in M. aeruginosa cultures upon treatment with T4. Therefore, we screened for bacteria that could degrade these toxins, and three new isolates (R12, S42 and S65) were identified. Simultaneous application of both T4 as a lytic agent and R12 or S42 as toxin-degrading bacteria could eliminate both Microcystis cells and its problematic toxin. Our eco-friendly approach, based on the application of newly isolated bacteria, provides a novel method to control harmful algal blooms.

The secretion of organics by living Microcystis under the dark/anoxic condition and its enhancing effect on nitrate removal

Recent studies indicated that the algal decomposition produces particulate and dissolved organic carbon (DOC), and can enhance denitrification in eutrophic lakes. However, the effects of the living cyanobacteria on nitrogen cycling in eutrophic lakes were still an unknown question. This study explores a new underlying mechanism of nitrate removal which is driven by living Microcystis. The results suggested that living Microcystis significantly enhanced the nitrate removal at sediment-water interface, with a nitrate removal rate of 0.54 d−1, which was 2.57 times higher than the nitrate removal rate in the treatment without the addition of Microcystis. Measurements of Chl a and Fv/Fm confirmed that Microcystis was tolerant to the dark/anoxic condition, and the recovery experiments suggested that Microcystis could survive under such stress conditions for at least seven days. Meanwhile, DOC secreted by living Microcystis reached to 4.55 mg C mg−1 Chl a. These secretions were biodegradable hydrophilic and contained carbohydrates and proteins. Our study indicated that during blooms, sinking Microcystis cells could directly provide DOC as carbon source, then consequently enhanced the denitrification at sediment-water interface, and the interactive relationship between living cyanobacteria and permanent nitrate removal should be taken into account while studying nitrogen cycling in aquatic ecosystem.

Harmful Algae Bloom Occurrence in Urban Ponds: Relationship of Toxin Levels with Cell Density and Species Composition.

Retention ponds constructed within urban watershed areas of high density populations are common as a result of green infrastructure applications. Several urban ponds in the Northern Kentucky, USA area were monitored for algal community (algae and cyanobacteria) from October 2012 to September 2013. Many of the harmful algal blooms observed during this study were composed primarily of the cyanobacteria genus, Microcystis. No correlations were observed between basic water quality parameters (dissolved oxygen, pH, conductivity, temperature, nitrate and soluble reactive phosphate) and the presence of cyanobacteria and/or microcystin cyanobacterial toxin levels. Furthermore, levels of microcystin toxins did not always coincide with high Microcystis cell counts. Harmful algal blooms in small urban ponds are common which pose risk to human and ecological health due to proximity of dense human population including pets and wild animals. Because harmful algal blooms were detected throughout the year in this study, adaptation of universal guidelines for the design, construction and maintenance of urban ponds may be necessary to protect watershed aquatic ecosystems, and lower health risks from exposure to such harmful blooms.

Bio-optical Properties of Cyanobacteria Blooms in Western Lake Erie

There is a growing use of remote sensing observations for detecting and quantifying freshwater cyanobacteria populations, yet the inherent optical properties of these communities in natural settings, fundamental to bio-optical algorithms, are not well known. Towards bridging this knowledge gap, we measured a full complement of optical properties in western Lake Erie during cyanobacteria blooms in the summers of 2013 and 2014. Our measurements focus attention on the optical uniqueness of cyanobacteria blooms, which have consequences for remote sensing and bio-optical modeling. We found the cyanobacteria blooms in the western basin during our field work were dominated by Microcystis, while the waters in the adjacent central basin were dominated by Planktothrix. Chlorophyll concentrations ranged from 1 to over 135 ${\mu}g/L$ across the study area with the highest concentrations associated with Microcystis in the western basin. We observed large, amorphous colonial Microcystis structures in the bloom area characterized by high phytoplankton absorption and high scattering coefficients with a mean particle backscatter ratio at 443nm greater than 0.03, which is higher than other plankton types and more comparable to suspended inorganic sediments. While our samples contained mixtures of both, our analysis suggests high contributions to the measured scatter and backscatter coefficients from cyanobacteria. Our measurements provide new insights into the optical properties of cyanobacteria blooms, and indicate that current semi-analytic models are likely to have problems resolving a closed solution in these types of waters as many of our observations are beyond the range of existing model components. We believe that different algorithm or model approaches are needed for these conditions, specifically for phytoplankton absorption and particle backscatter components. From a remote sensing perspective, this presents a challenge not only in terms of a need for new algorithms, but also for determining when to apply the best algorithm for a given situation. These results are new in the sense that they represent a complete description of the optical properties of freshwater cyanobacteria blooms, and are likely to be representative of bloom conditions for other systems containing Microcystis cells and colonies.

Evaluation of water quality during successive severe drought years within Microcystis blooms using fish embryo toxicity tests for the San Francisco Estuary, California

In the San Francisco Estuary, California, the largest estuary on the Pacific Coast of North America, the frequency and intensity of drought and associated cyanobacteria blooms are predicted to increase with climate change. To assess the impact of water quality conditions on estuarine fish health during successive severe drought years with Microcystis blooms, we performed fish embryo toxicity testing with Delta Smelt and Medaka. Fish embryos were exposed to filtered ambient water collected from the San Francisco Estuary during the Microcystis bloom season in 2014 and 2015, the third and fourth most severe recorded drought years in California. Medaka embryos incubated in filtered ambient waters exhibited high mortality rates (>77%), which was mainly due to bacterial growth. Medaka mortality data was negatively correlated with chloride, and positively correlated with water temperature, total and dissolved organic carbon, and ambient and net chlorophyll a concentration. Delta Smelt embryo mortality rates were lower (<42%) and no prominent seasonal or geographic trend was observed. There was no significant correlation between the Delta Smelt mortality data and water quality parameters. Aeromonas was the dominant bacteria that adversely affected Medaka. The growth of Aeromonas was suppressed when salinity was greater than or equal to 1psu and resulted in a significant reduction in mortality rate. Bacterial growth test demonstrated that the lysate of Microcystis cells enhanced the growth of Aeromonas. Toxin production by Microcystis is a major environmental concern, however, we conclude that dissolved substances released from Microcystis blooms could result in water quality deterioration by promoting growth of bacteria. Furthermore, a distinctive developmental deformity was observed in Medaka during the toxicity tests; somite formation was inhibited at the same time that cardiogenesis occurred and the functional heart was observed to be beating. The exact cause of the embryonic developmental deformity is still unknown.