No description available.

To initiate algal virus research in the Bay of Quinte, three stations were sampled biweekly throughout 2011. By targeting algal virus DNA polymerase, major capsid protein genes (MCP), and a Microcystis aeruginosa cyanophage (Ma-LMM01) tail sheath protein gene, PCR amplification revealed diverse and unique Phycodnaviruses (viruses of eukaryotic algae) and cyanophage. When analysed statistically, patterns of virus abundance suggested that the seasonality of any one virus cannot be generalised to predict that of other viruses, even among closely related viruses. This study also demonstrated a strong relationship between algal virus abundance and host biomass. It was found that despite the apparent heterogeneity of virus abundance across the Bay, virus abundance patterns clustered by sampling date and geographic location. By providing evidence for diverse algal viruses with complex seasonality, this work highlights significant gaps in the current understanding of Bay of Quinte phytoplankton ecology.

To initiate algal virus research in the Bay of Quinte, three stations were sampled biweekly throughout 2011. By targeting algal virus DNA polymerase, major capsid protein genes (MCP), and a Microcystis aeruginosa cyanophage (Ma-LMM01) tail sheath protein gene, PCR amplification revealed diverse and unique Phycodnaviruses (viruses of eukaryotic algae) and cyanophage. When analysed statistically, patterns of virus abundance suggested that the seasonality of any one virus cannot be generalised to predict that of other viruses, even among closely related viruses. This study also demonstrated a strong relationship between algal virus abundance and host biomass. It was found that despite the apparent heterogeneity of virus abundance across the Bay, virus abundance patterns clustered by sampling date and geographic location. By providing evidence for diverse algal viruses with complex seasonality, this work highlights significant gaps in the current understanding of Bay of Quinte phytoplankton ecology.

Cyanobacteria are one of the oldest forms of photosynthetic life and may have contributed significantly to the evolution of oxygen into the then anoxic environment. Cyanobacteria are also one of the best sources of natural secondary metabolites (cyanopeptides) some of which have harmful effects on the ecosystem, while others may be beneficial. It is known that these secondary metabolites are continuously produced during growth, however, it is not known whether the producing cyanobacteria actually benefit from these metabolites. The overarching aim of this study was to answer the question ‘Why do cyanobacteria produce secondary metabolites?’. With this aim in mind, preliminary work focused on understanding the growth and secondary metabolite production characteristics of Microcystis aeruginosa PCC7806. The technique of labelling secondary metabolites with 15N was successfully employed in differentiation and quantification of ex-novo and de-novo metabolites. The effect of exogenous cyanopeptides such as microcystins, aerucyclamides, anabaenopeptins, aeruginosamide, cyanopeptolin and aeruginosin on M. aeruginosa PCC7806 was evaluated using a rapid bioassay approach along with an automated cell enumeration technique. The results indicate that at least some cyanopeptides (microcystins-LR, microcystin-LF, aeruginosamide, anabaenopeptin B and aerucyclamide A) induce significant changes to cell division and metabolite production rate. In an ecological scenario, the release of such secondary metabolites by lysing cells (such as when blooms collapse), may be perceived as an alarm signal by surrounding live cells, which may in turn slow cell division and prepare for re-invasion. This may be a strategy for species survival and dominance. While the results from this study do not confirm a role for cyanopeptides, it is thought that the results are clearly indicative of the role played by cyanopeptides for the producing organism. In order to confirm a role, it is recommended that monitoring ribosomally synthesised metabolites (e.g. aerucyclamides) along with chlorophyll-a gene expression, with sophisticated techniques such as qPCR are used.

No description available.

No description available.

There is a current lack of accurate tools to determine the concentration of cyanobacteria in situ.  Besides, cyanobacterial blooms have to be carefully monitored in reservoirs as they are more frequent because of climate change and can lead to potential released of toxins, along with other components. This project investigates the possible use of fluorescent probes to measure the concentration of different types of organic matter released by the algae. Three different species of toxic cyanobacteria were chosen to carry out this research as they are representative of the local harmful blooms found across Australia. Furthermore, the efficiency of two different chemicals (powdered activated carbon, also known as PAC, and alum) used in drinking water treatment plants were investigated, in order to determine a method for automatic dosage adjustment in water treatment plant. The organic matter was characterized by LC-OCD and fluorescence spectroscopy and statistical analysis such as principal component analysis was performed on the generated data. General characterization of the different species was firstly performed and globally, similar comportments were observed among the three cyanobacteria species. There is indeed a general increase in the release of organic material throughout the cell’s growth phase. Results from the jar tests showed that PAC mainly targeted humic-like substances and building blocks, which are middle size particles. The average removal rate obtained was 40µg/L per mg/L of PAC added into the water. Therefore, there is indication that the decreased efficiency for the removal of the taste and odor compounds observed in certain plants can be partially attributed to direct competition of organic matter adsorption onto PAC instead of a blockage of the PAC pores by larger particles. On the other hand, alum was able to remove large particles, particularly biopolymers and also humic-substances. However, a great increase of the low molecular weight molecules at very high doses of alum was seen, which suggest that a too high dose of alum is toxic for the algae cells. Based on the bench scale testing the recommended dose of 50 mg/L seems to be optimum for the studied water treatment plant. Specific ultraviolet absorbance and dissolved organic carbon measurements were also investigated and good correlations were found between the concentration of humic-like substances and absorbance, confirming that they are good measure to assess the content of organic matter in the water. However, as the slope coefficient of the linear trend varied between the species, it was not possible to obtain a common conversion factor for all the species. Finally, one fluorophore was found in common to all the samples and is characterized by the excitation-emission wavelength: 240/440 nm. Correlations with the chromatography’s results were investigated and this component seems to match the biopolymers and humic-like substances concentrations. Furthermore, its intensity decreases continuously with the addition of PAC whereas a drop was observed at the lower doses of alum. In regards on these findings, a method for automatic chemicals dosing from the fluorescence measures was proposed. / Detta examensarbete handlar om hur dricksvattenkvalitet kan kontrolleras och övervakas i vattenreningsverk. Nu existerar  inte någon exakt metod för att bestämma koncentrationen av cyanobakterier i vatten då det finns många olika arter. Men det är viktigt att övervaka algers tillväxt in i vattenreningsverk för de kan släppa ut skadliga ämnen till dricksvattnet. De tre arter som studerats i detta projekt är giftiga. Det organiska materialet i råvattnet kan också blockera membranporer eller leda till n biprodukter, som är cancerframkallande. Till sist konkurrerar några organiska substansen med smak- och luktföreningar för adsorptionsställena hos det pulverformiga aktiverade kolet. Därför är smaken och luktföreningarna inte väl borttagna, vilket leder till kundernas klagomål. Cyanobakterier måste övervakas noggrant.                            För att bestämma biologisk och kemisk egenskap hos vatten används flera tekniker för närvarande. I examensarbetet har undersökningar med vätskekromatografi och fluorescensteknik företagits. Kromatografi användes för att klassificera den organiska substansen i mindre grupper: biopolymerer, humus substanser, byggstenar och neutralmolekyler med låg molekylvikt (LMVN). Statistisk analys med R, inklusive huvudkomponentanalys företogs på insamlade data. Fluorescensdata registrerades också och visas i en excitationsutsläppsmatris.                            Experimenten reproducerade en behandlingsprocess och undersökte effektiviteten hos två kemikalier: pulveriserat aktivt kol (PAK) och alun. Resultaten visade att humusämnen   och dess byggstenar var väl borttagna av PAK medan även biopolymerer och humusämnen var väl bortagna av alun. Emellertid var en för hög dos av alun skadlig eftersom det ledde till en ökad frisättning av LMVN. I synnerhert kunde PAK ta bort 40µg/L av både humusämnen och dess byggstenar per mg/L av PAK tillagd. Det föreslår att de är de viktigaste konkurrenterna och att endast direkt konkurrens för adsorptionsställena sker. Om det fanns blockeringsfenomen, skulle det också finnas en minskning för biopolymererna. Den optimala doseringen av alun som bestämdes för det undersökta vattenreningsverket var 50 mg/L. Det kunde ta bort 60-70% av biopolymerer och 40-50% av humusämnen.                            Specifik ultraviolett absorbans och fluorescens registrerades. Båda visade riktigt bra korrelationer med humusämnen, vilket gör de till bra verktyg för att bedöma vattenkvaliteten. Men det kräver fortfarande att arten av cyanobakterie urskiljs eftersom koefficientens lutningar var olika. De kan därför vara ett verktyg för att mäta koncentrationen av organisk material, men arten måste vara känd. Fluorescencedata visade en topp vid 440 nm. En parallellfaktoranalys utfördes på data och endast en komponent hittades gemensam i alla prover. Därför studerades den maximala fluorescensintensiteten hos denna komponent. Å ena sidan kunde vi observera en kontinuerlig minskning av intensiteten när PAK tillsattes. Det är därför möjligt att veta hur man justerar den kemiska doseringen från fluorescensintensiteterna. I slutet av examensarbetet föreslås en metod för automatisk kemisk dosering. Fluorescensprober kan ännu inte exakt indikera cellkoncentrationen. Men med flera sonder som riktar sig till olika våglängder kan de redan vara till stor hjälp för styrning vid vattenverk.

No description available.

The diploma thesis investigates the coagulation of nature waters with humic substances and peptides/proteins produced by Microcystis aeruginosa during water treatment process with aluminum coagulants. It was confirmed that the efficiency of coagulation mechanism of humic substances and peptides/proteins strongly depends on the pH value, because pH value is limited factor of a charge properties of peptides/proteins, humic substances and hyrolysis products of coagulants. The optimal pH range for the coagulation of humic substances was 5- 6 and for cyanobacterial peptides/proteins 5-6.5. In both cases a charge neutralisation and an adsorption were dominant mechanism of coagulation. Optimal pH range for the coagulation of humic substances in the presence of cyanobacterial peptides/proteins was identical as well as optimal pH range of humic substances with absence of peptides/proteins (5-6) but the presence of peptides/proteins positively influenced particle coagulation of humic substances, because the optimal concentration of the coagulants decreased to more than half. An interaction between humic substances and peptides/proteins was demonstrated. A positive effect of coagulation was observed in the case of jar tests with absence of coagulants at a very low pH range (<4). Keywords Humic substances; AOM...

The aim of the diploma thesis is to analyze the mechanisms involved in the coagulation of peptides and proteins contained in cellular organic matter produced by Microcystis aeruginosa, and to describe their influence on the coagulation of hydrophobic kaolin suspension. According to the results of jar tests, the coagulation effectiveness and removability of COM peptides/proteins and kaolin particles are heavily dependent on pH value which determines charge characteristics of peptides/proteins, kaolin and hydrolysis products of coagulant and therefore the prevailing mechanisms of interactions between them. Efficient coagulation and the highest removal of COM peptides and proteins were achieved in the pH range of 4-6 due to charge neutralization of peptide/protein negative surface by positively charged hydrolysis products of ferric coagulant. Peptides and proteins contributed to the coagulation of kaolin particles under the reaction conditions mentioned above, too. Charge neutralization and adsorption were found to be the dominant coagulation mechanisms under these conditions. At a low COM/Fe concentration ratio (COM/Fe < 0.33), adsorption of peptides/proteins onto ferric oxide-hydroxide particles, described as the electrostatic patch model, enabled the coagulation in the pH range of 6-8. On the...