Due to their specific effect on photosynthesis, herbicides pose a potential threat to coastal and estuarine microalgae. However, comprehensive understanding of the hazard and risk of these contaminants is currently lacking. Therefore the aim of the present study was to investigate the toxic effects of four ubiquitous herbicides (atrazine, diuron, Irgarol®1051 and isoproturon) and herbicide mixtures on marine microalgae. Using a Pulse Amplitude Modulation (PAM) fluorometry based bioassay we demonstrated a clear species and herbicide specific toxicity and showed that the current environmental legislation does not protect algae sufficiently against diuron and isoproturon. Although a low actual risk of herbicides in the field was demonstrated, monitoring data revealed that concentrations occasionally reach potential effect levels. Hence it cannot be excluded that herbicides contribute to observed changes in phytoplankton species composition in coastal waters, but this is likely to occur only occasionally.

A literature review on the effects of high ammonium concentrations on the growth of 6 classes of microalgae suggests the following rankings. Mean optimal ammonium concentrations were 7600, 2500, 1400, 340, 260, 100μM for Chlorophyceae, Cyanophyceae, Prymnesiophyceae, Diatomophyceae, Raphidophyceae, and Dinophyceae respectively and their tolerance to high toxic ammonium levels was 39,000, 13,000, 2300, 3600, 2500, 1200μM respectively. Field ammonium concentrations <100μM would not likely reduce the growth rate of most microalgae. Chlorophytes were significantly more tolerant to high ammonium than diatoms, prymnesiophytes, dinoflagellates, and raphidophytes. Cyanophytes were significantly more tolerant than dinoflagellates which were the least tolerant. A smaller but more complete data set was used to estimate ammonium EC50 values, and the ranking was: Chlorophyceae>Cyanophyceae, Dinophyceae, Diatomophyceae, and Raphidophyceae. Ammonia toxicity is mainly attributed to NH3 at pHs >9 and at pHs <8, toxicity is likely associated with the ammonium ion rather than ammonia.

Effects of the antimicrobial agent triclosan to natural periphyton communities (biofilms, comprising primarily microalgae and bacteria) were assessed in two independent experiments during spring and summer. For that purpose a semi-static test system was used in which periphyton was exposed to a concentration range of 5–9054nmol/L triclosan. Effects on algae were analyzed as content and composition of photosynthetic pigments. The corresponding EC50 values were 39.25 and 302.45nmol/L for the spring and summer experiment, respectively. Effects on periphytic bacteria were assessed as effects on carbon utilization patterns, using Biolog Ecoplates. No inhibition of either total carbon utilization or functional diversity was observed, indicating a pronounced triclosan tolerance of the marine bacteria. In contrast, a small stimulation of the total carbon utilization was observed at triclosan concentrations exceeding 100nmol/L.

The effects of long-line mussel farming on microphytobenthos were investigated in a coastal area of the Gulf of Trieste. Sediment grain-size, organic matter content, microalgal abundance and community structure were analysed in September 2008 and March 2009. Four areas were sampled: a twenty-year farm, a four-year farm, a disused farm and a reference site. Principal component analysis (PCA) highlighted a decreasing gradient of organic matter content from the twenty-year farm to the control. Mussel farming seemed to influence microphytobenthic abundance with higher densities in the oldest farm. Three genera were dominant; Navicula and Gyrosigma seemed to be stimulated by the organic load under the active farms while we infer that Nitzschia proliferation was limited by shade caused by mussel ropes. In the PCA, samplings of the disused farm were placed in-between the still active farms and the control, indicating the partial recovery occurred in this site.

To biocontrol algal bloom, a novel algicidal bacterium, Enterobacter sp. NP23, was isolated. This strain has an effective algicidal activity against Chlorella vulgari, Microcystis aeruginosa, Scenedesmus, and Chlorella pyrenoidosa. Meanwhile, the growth factors were assayed to obtain a high cell density of strain NP23. As a result, three growth factors (i.e., KNO₃0.6 %, MnSO₄·H₂O 0.001 %, and K₂HPO₄0.3 %) were determined as the critical roles in enhancing the cell density of 10¹³ CFU/mL. Moreover, algicidal activity assays revealed that strain NP23 exhibited high algicidal activities against M. aeruginosa and Scenedesmus. These results indicate that this wild-type strain would provide a new member for biocontrolling microalgal and cyanobacterial populations in eco-technology.

In this study, Scenedesmus quadricauda ABU12 was immobilized with sodium alginate to determine its potential for decolorizing indigo blue dye under different incubation conditions. The microalga was incubated at different pH (6.5–9.5), biomass concentrations (0.1–1.0 g l⁻¹), dye concentrations (12–75 mg l⁻¹) and temperatures (25–40°C). The concentration of biomass used significantly determined the rate of dye decolorization, as the lowest biomass concentration (0.10 g) was able to completely decolorize the dye by day 3, while the highest biomass concentration (1.00 g l⁻¹) attained 100 % decolorization on day 4. Neutral pHs supported the highest dye decolorization rates compared alkaline pHs. The rate of dye decolorization had a linear relationship with the concentration of the dye in solution as increasing dye concentration in the medium significantly reduced the rate of decolorization (p < 0.05). At 25°C, the rate of dye decolorization was consistently higher from day 2 to the end of the experiment. Infra-red analyses of the algal biomass and the dye solution was done in Kbr by pressing between flat aperture plates of sodium chloride and scanning from 4,000 to 625 cm⁻¹. This revealed the presence of functional groups associated with the biomass and dye that provided possible explanations for the decolorization of the dye under the different incubation conditions. These results showed that immobilized S. quadricauda is capable of decolorizing indigo blue dye at low biomass when immobilized with sodium alginate. However, this was dependent on the incubation temperature and dye concentration.

Modern society grapples with large amounts of household waste. The anaerobic digestion of this waste offers a promising source for energy-rich biogas production but generates high toxic effluents that require treatment before reuse or disposal into the environment. This study aimed to investigate three techniques, namely coagulation/flocculation, electro-coagulation, and activated sludge, in terms of efficiency in the treatment of these effluents. It also aimed to assess their toxicity effects on the germination and growth of durum wheat Triticum aestivum L. seeds before and after 6 days of treatment. Activated sludge was most efficient in reducing chemical oxygen demand, turbidity, and conductivity (95.7 %, 15.8 %, and 37.5 %, respectively). The effluent treated with this technique induced a marked delay in germination (low mean time of germination) and a significant reduction in the percentages of seed germination and root and leaf growths. It was also noted to strongly induce lipid peroxidation in roots and leaves, which presumably explained the germination/growth inhibition of the wheat seeds. The effluent also induced marked lipid peroxidation effects and strongly inhibited the activities of butyrylcholinesterase in mice bone marrows. The effluent shows a high ability to inhibit the growth of three microalgae; these endpoints are useful tools to biomonitor the physico-chemical quality of this wastewater. Overall, while no significant alterations were observed in terms of animal and vegetable toxicities when the effluent was treated by coagulation/flocculation, activated sludge treatment proved efficient in reducing the toxicities induced by the untreated effluents. The results indicate that the application of this technique is promising with regards to attaining efficient, eco-friendly, and cost-effective strategies for the management and treatment of household waste.

In the actual environment, temperatures fluctuate drastically through season or global warming and are thought to affects risk of pollutants for aquatic biota; however, there is no report about the effect of water temperature on toxicity of widely used herbicide diuron to fresh water microalgae. The present research investigated inhibitory effect of diuron on growth and photosynthetic activity of a green alga Pseudokirchneriella subcapitata at five different temperatures (10, 15, 20, 25, and 30 °C) for 144 h of exposure. As a result, effective diuron concentrations at which a 50 % decrease in algal growth occurred was increased with increasing water temperature ranging from 9.2 to 20.1 μg L–¹for 72 h and 9.4–28.5 μg L–¹for 144 h. The photochemical efficiency of photosystem II (Fᵥ/Fₘratio) was significantly reduced at all temperatures by diuron exposure at 32 μg L–¹after 72 h. Inhibition rates was significantly increased with decreased water temperature (P < 0.01). Intracellular H₂O₂levels as an indicator of oxidative stress were also decreased with increasing temperature in both control and diuron treatment groups and were about 2.5 times higher in diuron treatment groups than that of controls (P < 0.01). Our results suggest water temperatures may affect the toxicokinetics of diuron in freshwater and should therefore be considered in environmental risk assessment.