Intracellular Organic Matter Research Articles

Coagulation and disinfection by-products formation potential of extracellular and intracellular matter of algae and cyanobacteria.

Coagulation and flocculation can remove particulate algal cells effectively; however, they are not very effective for removing dissolved algal organic matter (AOM) in drinking water plants. In this work, optimum coagulation conditions using alum for both extracellular and intracellular organic matter of six different algal and cyanobacterial species were determined. Different coagulation conditions such as alum dosage, pH, and initial dissolved organic carbon (DOC) were tested. Hydrophobicity, hydrophilicty, and transphilicity of the cellular materials were determined using resin fractionation method. The removal of DOC by coagulation correlated well with the hydrophobicity of the AOM. The disinfection by-product formation potential (DBPFP) of various fractions of AOM was determined after coagulation. Although, higher removal occurred for hydrophobic AOM during coagulation, specific DBPFP, which varied from 10 to 147 μg/mg-C was higher for hydrophobic AOM. Of all the six species, highest DBPFP occurred for Phaeodactylum tricornutum, an abundant marine diatom species, but is increasingly found in surface water.

Effects of pre-ozonation on the cell characteristics and N-nitrosodimethylamine formation at three growth phases of Microcystis aeruginosa.

Pre-oxidation in water treatment is considered an effective method to enhance the removal of algal cells and their exuded organic matters. However, pre-oxidation also alters the characteristics of algae and consequently influences disinfection processes. The existing studies mainly focused on the stationary growth phase, but little is known for the exponential and declined phases. The objectives of this study were to examine the effects of pre-ozonation on the integrity of algal cells, the release of algal organic matters, and the formation of disinfection by-products like N-nitrosodimethylamine (NDMA) from Microcystis aeruginosa (M. aeruginosa) at three growth phases. The results demonstrated that pre-ozonation was efficient to inactivate M. aeruginosa cells. The severity of M. aeruginosa cell damage increased as the ozone dosage increased from 0.5 to 2.0mg/L. The damage of cell membranes resulted in the release of intracellular organic matters. Excitation-emission matrix spectra (EEMS) analysis indicated that ozone mainly reacted with soluble microbial products (SMP). With the increase of ozone concentration, although the trend of NDMA formation was similar for all three growth phases, more production of NDMA by algal cells was observed at the declined phase. In the post-disinfection process, chloramine showed the potential as a more suitable disinfectant than chlorination after pre-ozonation to minimize the NDMA formation. Therefore, appropriate pre-ozonation is beneficial to reduce the NDMA formation from exponential algae, while has no significant change during both stationary and declined phases.

Effects of ultrasound on Microcystis aeruginosa cell destruction and release of intracellular organic matter.

Harmful algal blooms negatively impact ecosystems and threaten drinking water sources. One potential method to effectively counteract algal blooms is ultrasonication. However, ultrasonication can easily lead to the release of intracellular organic matter (IOM). The purpose of this study was to investigate the relationship between the destruction of algal cells and IOM release at different ultrasound frequencies. Microcystis aeruginosa cells were ultrasonicated at 20kHz with an intensity of 0.038W/mL, 740kHz with an intensity of 0.113W/mL, and 1120kHz with an intensity of 0.108W/mL. The IOM release was detected by fluorescence spectroscopy in addition to the more commonly used haemocytometry and optical density. After ultrasonication for 15min, the removal rate of algal cells reached 10.5% at 20kHz, 9.46% at 740kHz, and 35.4% at 1120kHz. The 20kHz and 740kHz ultrasound caused local damage to algal cells and then disrupted them, whereas the 1120kHz ultrasound directly disrupted most algal cells. The extracellular organic matter (EOM), which was increased by ultrasonication, mainly consisted of protein-like compounds, chlorophyll, and a small amount of humic-like substances. Gas vacuoles had been destructed before the cells were broken, as indicated by the decrease of cell size and the wrinkles on the cell surface. Moreover, the removal of algae cells while upholding integrity is more conducive to the safety of the water environment.

The effect of low frequency ultrasonic treatment on the release of extracellular organic matter of Microcystis aeruginosa

The effect of low frequency ultrasonic treatment on the growth of cyanobacteria and the behavior of extracellular organic matter (EOM) were investigated in this study. The growth of cyanobacteria can be controlled effectively by low frequency ultrasonic treatment, and the inhibitory effect of ultrasound on the photosynthetic ability of cells was more significant than on the cells density (the minimum values of cells density and chlorophyll-a was obtained at day 3 and day 1 respectively). Significant rupture of cells was observed when irradiated by a higher intensity ultrasound (ultrasonic dosage ≥ 1.5 J/mL). Tyrosine-like components were mainly distributed in the soluble EOM and loosely bound EOM fractions; both of the tryptophan-like components and polyaromatic humic-like components were distributed in the soluble EOM, loosely bound EOM, and tightly bound EOM fractions; and polycarboxylate humic-like components were mainly distributed in soluble EOM fraction. Given that the production of hydroxyl radicals was measured, negligible due to the limit of ultrasonic treatment duration (≤1 min). On the other hand, intensive shock waves and shear forces of collapsing acoustic cavitation bubbles were considered as the main reason for the rupture of cells and the changes of the behavior of EOM. A higher intensity ultrasonic treatment resulted in a greater release of EOM, including bound EOM (ultrasonic dosage ≥ 0.1 J/mL), and intracellular organic matter (ultrasonic dosage ≥ 1.5 J/mL). Moreover, the determination of protein and polysaccharide suggested that the bonding of polysaccharides to cells surface is stronger than that of proteins to cells surface, and a portion of the polysaccharides in other fractions was transferred to the tightly bound state during the first serval days after ultrasonic treatment.

Removal of Microcystis aeruginosa and control of algal organic matters by potassium ferrate(VI) pre-oxidation enhanced Fe(II) coagulation

The problem of cyanobacteria blooms during potable water production has generated wide concern. Ferrate(VI) serving as a pre-oxidation tactic was first applied to enhance conventional Fe(II) coagulation for Microcystis aeruginosa-laden water treatment at lab scale. Results demonstrated that ferrate(VI) pre-oxidation could successfully destabilize algae cells through destroying the protective organic layer. The residual ferrate(VI) together with post-added Fe(II) could provoke a comproportionation reaction, where large amounts of Fe hydrolyzates [Fe(OH)3] are formed. The in-situ Fe(OH)3 with abundant reactive surface is responsible for the promotion of flocs growth by facilitating the clustering and cross-linking of algal organic matters (AOM) and cyanobacteria cells, simultaneously resulting in satisfactory reductions in OD680, turbidity and UV254. Overdose of ferrate(VI) could cause severe cell destruction along with the release of intracellular organic matter (IOM), which may impair the water quality by increasing the concentration of dissolved organic carbon (DOC) and the disinfection by-products formation potential (DBPFP). Meanwhile, considering the Fe residual in settled water, the optimal ferrate(VI) dose (20 µM) and Fe(II) dose (80 µM) were proposed. Besides, the synergistic effect of both the degradation by ferrate(VI) and the adsorption by in-situ Fe(OH)3 contributed to the removal of DOC and Microcystin-LR. This study suggests that ferrate(VI) might be a potential candidate for pre-treatment to assist Fe(II) coagulation when addressing algae-laden water.

Influence of algal organic matter of Microcystis aeruginosa on ferrate decay and MS2 bacteriophage inactivation

Surface water contaminated with algae and with enteric viruses is a global problem. When surface water is used as a drinking water source, it is important to know the influence of algal organic matter on the disinfection of viruses. In this work, we studied the disinfection efficacy of ferrate and the influence of algal organic matter on the disinfection. We determined the MS2 inactivation kinetics by ferrate under three pH conditions (7, 8, and 8.7). The experimental results and pH-dependent calculation suggest that H2FeO4 and HFeO4− are 1935 and 8 times as effective as FeO42− in MS2 inactivation. We also found that intracellular algal organic matter (IAOM) had a stronger effect on MS2 inactivation kinetics than extracellular algal organic matter (EAOM) suggesting that IAOM led to higher consumption of Fe(VI) compared to EAOM. At pH 8.7, while significant consumption of FeO42− by as low as 8 mg C/L of EAOM and 2 mg C/L of IAOM was detected, MS2 inactivation was negatively influenced only when 13 mg C/L of IAOM present. This study showed that it is important to control pH and to determine the concentration of algal organic matter if ferrate is used for disinfection of surface water contaminated with algae.

Fast photocatalytic inactivation of Microcystis aeruginosa by metal-organic frameworks under visible light

In this work, Metal-organic Frameworks (MOFs) were applied to inactivate algae under visible light with low doses. Five MOFs with different compositions (Zn and Fe; carboxylates or imidazolates) were successfully synthesized and characterized by XRD, SEM and UV–vis. The effects of MOFs on Microcystis aeruginosa were evaluated with regard to morphology characteristics, physiological activity, cell integrity and pigment degradation. The results indicated that Ag/AgCl@ZIF-8 outperformed MOF-235, ZIF-8, Bi2WO6/MIL-100(Fe) and BiOBr/MOF-5 in the degradation of chlorophyll a at the dose of 10 mg L−1. After 6 h of irradiation, 93.1% of Microcystis aeruginosa died and was unable to regrow and reproduce, which was demonstrated by changes in cell morphology, damage of cell membrane integrity and antioxidant enzyme system. Besides, the intracellular organic matter (IOM) and extracellular organic matter (EOM) were proven to be efficiently removed by MOF-assisted photocatalytic inactivation. Superoxide radical (O2·-) was demonstrated to be the major reactive oxygen species. A probable mechanism was proposed that the electrons in the valence band of Ag/AgCl@ZIF-8 transfer into the conduction band under irradiation to produce O2·- which inactivated the algae cells. Furthermore, Ag/AgCl@ZIF-8 can effectively remove Microcystis aeruginosa under sunlight and is of great application prospects for algae removal in real water bodies.

Aerobic denitrification performance of strain Acinetobacter johnsonii WGX-9 using different natural organic matter as carbon source: Effect of molecular weight

The aim of this study was to investigate the effect of natural organic matter (NOM) including humic acid (HA) and fulvic acid (FA), intracellular organic matter (IOM) extracted from Microcystis aeruginosa (MA) and Chlorella sp. (CH), and their different molecular weight (MW) fractions on the aerobic denitrification performance of bacterial strain WGX-9 by monitoring nitrogen removal efficiency and testing changes in organic matter with HA, FA, MA-IOM and CH-IOM as the sole carbon source. Strain WGX-9 was identified as Acinetobacter johnsonii and exhibited excellent aerobic denitrification capability. The nitrate removal efficiency with IOM as the sole carbon source was relatively higher than that with NOM as the sole carbon source. The prepared NOM and extracted IOM samples were separated into six fractions with MW cut-offs of 100, 30, 10, 5 and 1 kDa. The fraction of MW > 100 kDa contributed the largest amount to the MW distribution, accounting for 77.11%, 29.00%, 44.97% and 24.81% of HA, FA, MA-IOM, and CH-IOM, respectively. Nitrate removal efficiency was improved with decreasing MW of organic matter. For example, nitrate removal efficiency was 26.50%, 32.41%, 27.88% and 43.89% using HA, FA, MA-IOM, and CH-IOM fractions of MW > 100 kDa as the carbon source, whereas with MW < 1 kDa, it increased to 36.67%, 37.88%, 60.90%, and 68.90%, respectively. This is probably because the smaller MW fraction is more suitable for bacterial growth. These results demonstrate that the strain WGX-9 can utilize lower MW organic matter, which lays the foundations for nitrogen removal in actual drinking water reservoirs.

Evaluation of disruption/permeabilization methodologies for Microcystis aeruginosa as alternatives to obtain high yields of microcystin release

The extraction of the wide range of useful bioactive compounds produced by cyanobacteria is still a major bottleneck at industrial scale. In addition to the high costs, extraction efficiencies are also commonly low, with low cell disruption efficiencies playing a particularly significant role in intracellular compounds' release. To increase the chances of an extended use of the cyanobacteria toxin microcystin in several biotechnological fields, we aimed to optimize five different disruption techniques: bead milling, microwave, freeze-thaw cycles, high-speed homogenization, and sonication. For each of the methods tested, the conditions that maximized the intracellular organic matter release were: i) 20% of beads and treatment time of 7 min (bead milling); ii) 800 W for 1.5 min (microwave); iii) three 12-h freeze-thaw cycles at −20 °C; iv) 15,000 rpm for 7 min (high-speed homogenization); and v) 40 kHz for 10 min (sonication).Sonication and freeze-thaw cycles followed by sonication revealed to be the most effective methodologies to ensure a maximum intracellular organic matter release and, consequently, microcystin availability for being extracted. The decrease of cells' viability was however more evident in freeze-thaw cycles, freeze-thaw cycles followed by sonication, and microwave where only 0.3, 0.05 and 0.9% of the initial cells, respectively, maintained their viability after being treated. On the other hand, sonication and bead milling reduced the viability of the original culture to 5 and 15.5%, respectively, while high-speed homogenization did not show any significant differences compared to control.According to the results obtained in this study, the most suitable methodology to maximize the release of microcystin was therefore the use of sonication (40 kHz) during 10 min.

Using Advanced Spectroscopy and Organic Matter Characterization to Evaluate the Impact of Oxidation on Cyanobacteria.

Drinking water treatment plants throughout the world are increasingly facing the presence of toxic cyanobacteria in their source waters. During treatment, the oxidation of cyanobacteria changes cell morphology and can potentially lyse cells, releasing intracellular metabolites. In this study, a combination of techniques was applied to better understand the effect of oxidation with chlorine, ozone, potassium permanganate, and hydrogen peroxide on two cell cultures (Microcystis, Dolichospermum) in Lake Champlain water. The discrepancy observed between flow cytometry cell viability and cell count numbers was more pronounced for hydrogen peroxide and potassium permanganate than ozone and chlorine. Liquid chromatography with organic carbon and nitrogen detection was applied to monitor the changes in dissolved organic matter fractions following oxidation. Increases in the biopolymer fraction after oxidation with chlorine and ozone were attributed to the release of intracellular algal organic matter and/or fragmentation of the cell membrane. A novel technique, Enhanced Darkfield Microscopy with Hyperspectral Imaging, was applied to chlorinated and ozonated samples. Significant changes in the peak maxima and number of peaks were observed for the cell walls post-oxidation, but this effect was muted for the cell-bound material, which remained relatively unaltered.

Study on ultrasonic treatment for municipal sludge.

Ultrasonic technique has attracted wide attention due to its advantages of no secondary pollution, high decomposition speed and simple equipment in the treatment of municipal sludge. In this paper, study on ultrasound-chemical treatment for municipal sludge in investigated. Results indicate that ultrasonic waves can destroy sludge floc structure and cell walls, release intracellular organic matter, and accelerate the hydrolysis process; ultrasonic can improve the sedimentation and dewatering performance of sludge; ultrasonic wave can produce a sponge effect on sludge, which makes the water flow through the channel more easily from the wave surface, thereby agglomerating the sludge particles and increasing the particle size; ultrasound can promote coagulation; ultrasound can also improve the activity of excess sludge, and improve the efficiency of anaerobic digestion process and the final biogas production. Ultrasound-Cationic polyacrylamide (CPAM) treatment can undermine the repulsion between particles to a certain extent and destabilizes sludge flocs. In addition, the adsorption and bridging action of the flocculant CPAM further agglomerates the sludge particles, and the water in the sludge is squeezed out to be converted into free water, which further improves the dewatering performance of the sludge, thereby reducing the moisture content of the filter cake.

Impact of UV irradiation on Chlorella sp. damage and disinfection byproducts formation during subsequent chlorination of algal organic matter

The frequent occurrence of algal blooms in surface water has attracted more and more attention, which caused many water quality problems, including disinfection byproducts (DBPs). Algal organic matter (AOM) including intracellular organic matter (IOM) and extracellular organic matter (EOM), was a well-known precursor to DBPs formation in drinking water. This study evaluated the effect of ultraviolet (UV) irradiation on the cell integrity, IOM release and DBPs formation during subsequent chlorination of Chlorella sp. Results showed the damage rates of algal cells increased to 40.1% after the high UV irradiation of 528 mJ/cm2, which contributed to the release of IOM. In addition, UV irradiation was effective in reducing the formation of haloacetic acids (HAAs) both in AOM and IOM, but promoted the formation of nitrogenous DBPs (N-DBPs) from AOM in subsequent chlorination. Furthermore, neutral pH exerted a positive effect on the formation of DBPs. UV irradiation decreased the bromine substitution factor (BSF) value of AOM at a high bromide level. The BSF values increased with increasing of the concentration of bromide. Moreover, more amino acids and low molecular weight precursors were produced after UV irradiation in filtered supernatant, which contributed to the formation of N-DBPs with algal chlorination. Overall, this information demonstrated pre-oxidation of UV irradiation could be used to treat the algal-rich drinking water.

•OH Inactivation of Cyanobacterial Blooms and Degradation of Toxins in Drinking Water Treatment System

Cyanobacterial blooms continue to serve as one of the most serious global issues threatening water supply and human health. During cyanobacterial bloom season, a large •OH-yield equipment was developed and installed after coagulation settling in a 12000 ton/day drinking water treatment system in Xiamen, China. An •OH concentration of 7.76∼57.8 μmol/L was formed by using the oxygen activated species generated by strong ionisation discharge combining with the effect of water jet cavitation. •OH pre-treatment at a dose of 1.0 mg/L inactivated cyanobacterial blooms in the process of conveying bloom water within only 20s, which were then removed by sand filtration. Under SEM observation, dominant Microcystis sp. colonies connected by mucilage were dispersed into individuals that still retained the cell integrity, indicating no release of intracellular organic matter (IOM). According to a flow cytometry analysis, the main cause of •OH inactivation was the breakage of DNA strands. Meanwhile, the •OH-mineralized microcystin-LR was by breaking the C=C conjugated diene bond and crucial opening the persistent benzene ring to carboxylic acid m/z 158.0. During •OH pre-treatment of 1.0 mg/L and NaClO disinfection of 0.5 mg/L, all water quality indexes and disinfection by-product (DBP) contents complied with the Chinese Sanitary Standards for Drinking Water. Therefore, the •OH based on the strong ionisation discharge showed great prospect for large-scale drinking water treatment in the removal of cyanobacterial blooms while retaining cell integrity as well as the degradation of toxins.

Evaluation of disinfection byproduct formation from extra- and intra-cellular algal organic matters during chlorination after Fe(vi) oxidation.

Blue-green algae commonly bloom in fresh water in summer, producing extra- and intra-cellular algal organic matters, which are important precursors for disinfection byproduct (DBP) formation. In this study, we evaluated the effect of pre-oxidation with ferrate(vi) (FeO42−, Fe(vi)) on the characterization of intracellular organic matter (IOM) and extracellular organic matter (EOM). The results indicated that soluble microbial-like products of EOM and IOM decreased and humic acid-like products of IOM increased, which would influence the DBP formation in the subsequent chlorination step. Therefore, in this study, the effect of Fe(vi) pre-oxidation on the DBP formation from IOM and EOM with subsequent chlorination was also investigated. For Chlorella sp., EOM presented no significant change, and IOM presented a reduction of THMs (8.2%) after Fe(vi) oxidation at a dosage of 16 mg L−1. For P. limnetica, EOM and IOM both exhibited reduction of trihalomethanes (THMs) and chloral hydrate (CH) after Fe(vi) oxidation. Besides, THMs had the lowest concentration at pH 8.0 in all four solutions. Haloacetonitriles (HANs) and haloketones (HKs) showed slight changes with increasing pH values. Due to the frequent detection of bromide (Br−) in surface water, the effect of bromide existence on THM formation was also investigated. The results indicated that all brominated DBPs increased, and chlorinated DBPs decreased with the increase in bromide concentration. In addition, the bromine substitution factor (BSF) of Chlorella sp. and P. limnetica both increased with the increase in Br− concentration.

Impact of Graphene Oxide on Algal Organic Matter of Microcystis aeruginosa

Graphene oxide (GO) as a novel and promising material has a huge market and multiple applications. The release of GO into the aquatic system during their life cycle would lead to potential risks for the environment and aquatic organisms. This study evaluated the impacts of GO on algal growth and algal organic matter (AOM) of Microcystis aeruginosa. GO exhibited moderate effects on algal growth and the photosynthetic system. There was no evident influence on cell density and chlorophyll-a content at GO concentrations below 10 mg/L. Variation and characteristics of AOM after the interaction between GO and algae were analyzed. The characteristics of intracellular organic matter on algae’s exposure to GO showed no significant difference compared with the control group. Conversely, GO had greater impacts on extracellular organic matter after the interaction with algae. The dissolved organic carbon and microcystin-LR showed a significant decline with the increasing GO concentration. The overall molecular weight decreased as well, typically for low molecules. Moreover, the three-dimensional fluorescence spectrum showed that the humic acid- or fulvic acid-like organics decreased obviously. These conclusions reflect that GO has a strong adsorption capacity for removing extracellular organic matter, whereas it did not inflict damage to the algal cells, so that little change could be found in intracellular organic matter. The current study is expected to be beneficial in interpreting the potential risks of GO on algal growth and the variation of AOM.

Fluorescent and molecular weight dependence of THM and HAA formation from intracellular algogenic organic matter (IOM)

This study (i) examined the formation of two major carbonaceous disinfection by-products (C-DBPs), trihalomethanes (THMs) and haloacetic acids (HAAs), during the chlorination of intracellular algogenic organic matter (IOM) extracted from two commonly blooming algae M. aeruginosa (MA) and Chlorella sp. (CH), and (ii) investigated the roles and relationships of fluorescent and molecular weight (MW) properties on/with IOM-derived THMs and HAAs. The extracted IOM samples were separated into different MW fractions by centrifugal devices with membrane support with MW cut-offs of 100, 30, 10, 3, and 1 kDa. We observed an overall reduction of C-DBPs with a decrease of IOM-MW from >100 kDa to <1 kDa. Of six fractionated IOM, a large fraction (>100 kDa) contributed the largest amount to the MW distribution of IOM, accounting for 33 and 42% of the total dissolved organic carbon (DOC) of MA and CH, respectively. It also had the highest-yielding potential to produce significant levels of THMs and HAAs, and total C-DBPs over other small MW fractions. Although small MW fractions (>10 kDa) contributed around 50% of the total DOC, they made an insignificant contribution (>20%) to the THMs, HAAs, and overall C-DBPs. Furthermore, the decrease of IOM MW caused a shift from the domination of HAA formation to THM formation, especially when MW was <10 kDa. By canonical correspondent analysis, the relationship of IOM-derived THMs and HAAs with IOM properties was examined. In particular, large fractions of IOM, exhibiting aromatic protein- (AP) and soluble microbial product- (SMP) like fluorescence, are favorable for the formation of HAAs, whereas small MW fractions of IOM with HA- and FA-like fluorescence preferentially tends to form THMs. Our findings evidently show the strong dependence of IOM-derived THMs and HAAs on the fluorescent and MW properties. Therefore, the characterization of MW and fluorescent properties can provide the advantages in the control of algae-derived DBPs upon the chlorination of eutrophic water.

Algal fouling control in a hollow fiber module during ultrafiltration by angular vibrations

In this work, a lab-scale membrane system was developed to accommodate angular vibrations with a hollow fiber module. A series of filtration experiments were designed and implemented to investigate the effects of angular vibrations on fouling by various algae-derived foulants, including algal cells, debris, extracellular organic matter (EOM), and intracellular organic matter (IOM). The experimental results indicated the effects of angular vibrations on fouling mitigation at the frequency of 2 Hz in the following order: algal cells (~ 97.4%) > debris (~ 93.6%) > IOM (~ 81.8%) > EOM (~ 52.3%). The vibrations mainly targeted the cake layer formed by these foulants, but was ineffective for pore blocking which constituted a large portion of EOM fouling. Although the fouling rates were accelerated during the normal ultrafiltration of the combined foulants, the effects of angular vibrations continued to be impressive (67.8–92.6%). This was because the cake layer formation was the dominant fouling mechanism. Furthermore, the vibrations were found to improve the organic removal by alleviating concentration polarization. In this paper, quantitative analysis is presented to demonstrate the potential of angular vibrations to control algal fouling with the relatively low energy consumption of 0.034 mW.

Influence of algal organic matter on MS2 bacteriophage inactivation by ultraviolet irradiation at 220 nm and 254 nm

We determined the potential interference of extracellular algal organic matter (EAOM) and intracellular algal organic matter (IAOM) extracted from Microcystis aeruginosa on MS2 bacteriophage inactivation under UV irradiation at two wavelengths (220 and 254 nm). UV irradiation at 220 nm doubled the inactivation rate of MS2 in water containing EAOM than in organic-free phosphate buffered solution. In contrast, EAOM did not change MS2 inactivation by exposure to UV 254 nm. The presence of IAOM did not significantly influence MS2 inactivation by exposure to either UV 254 or UV 220 nm. To achieve 3 log10 inactivation of MS2, UV254 nm required more than double the dose of UV220 nm (45 mJ/cm2 vs. 20 mJ/cm2). Linear correlations between the reduction in infectivity and the reduction in genome copies detected by reverse transcription quantitative polymerase chain reaction suggested that genomic damage is the main mechanism responsible for MS2 inactivation in water containing algal organic matter (AOM) by exposure to UV irradiation. These findings suggest that the presence of AOM did not negatively influence MS2 inactivation by either 220 or 254 nm irradiation, and that a lower UV dose of 220 nm irradiation can be used to achieve the same level of inactivation in water containing AOM.

Formation characteristics of carbonaceous and nitrogenous disinfection by-products depending on residual organic compounds by CGS and DAF

Allogenic organic matter (AOM) composed of extracellular and intracellular organic matter (EOM and IOM) is a major precursor of halogenated carbonaceous and nitrogenous disinfection by-products (C-DBPs and N-DBPs) upon chlorination. The EOM and IOM extracted from Microcystis aeruginosa were analyzed based on bulk parameters and organic fractions with different molecular weight by liquid chromatography with organic carbon detection (LC-OCD). It investigated the efficiency of a conventional gravity system (CGS) and dissolved air flotation (DAF) in the removal of organic precursors, together with measurement of the formation of four major trihalomethanes (THMs) and haloacetonitriles (HANs) in treated water upon chlorination. The results showed that EOM accounted for 59% of building blocks and humic substances, whereas for IOM, 54% were low molecular weight (LMW) neutrals. Both CGS and DAF showed 57-59% removal of dissolved organic carbon (DOC) from EOM and IOM. Regarding DON removal, DAF was found to be more effective, i.e., 8% higher than CGS for EOM. Moreover, the removal of LMW acids and neutrals (not easy to remove and are major precursors of DBPs) from EOM and IOM by DAF was higher than from CGS. The amounts of DBPs measured in all the samples treated for interchlorination were much lower than in the samples for prechlorination. Although the precursors of EOM had a higher concentration than in IOM, THMs and HANs were detected for IOM at a higher concentration, which might be attributed to higher amounts of aromatic, aliphatic moisture and protein compounds in the IOM. Comparatively, DAF showed lower THM and HAN values than CGS water, particularly for IOM. Also, DAF showed a sharp decrease in THMs and an insignificant increase in HANs according to time.

Environmental risks of ZnO nanoparticle exposure on Microcystis aeruginosa: Toxic effects and environmental feedback

The vast majority of studies measure the toxic effect of organisms exposed to nanoparticles (NPs) while there is still a lack of knowledge about the influence of NPs on the aquatic environment. It is unknown whether or not the interaction between NPs and algae will result in the variation of algal organic matter (AOM) and stimulate the production of more algal toxins. In this study, zinc oxide nanoparticles (nano-ZnO) as a typical representative of metal oxide NPs were used to evaluate the toxic effects and environmental feedback of Microcystis aeruginosa. Reactive oxygen species (ROS) and malondialdehyde (MDA) were measured to explain the toxicity mechanism. Changes of AOM, including the production of toxins, the molecular weight distribution and the excitation-emission matrices of algal solution were also studied as environmental feedback indicators after nano-ZnO destroyed the algae. As the nano-ZnO exceeded the comparable critical concentration (1.0 mg/L), the algae were destroyed and intracellular organic matters were released into the aquatic environment, which stimulated the generation of microcystin-LR (MC-LR). However, it is worth noting that the concentration of nano-ZnO would need to be high (at mg/L range) to stimulate more MC-LR production. These findings are expected to be beneficial in interpreting the toxicity and risks of the releasing of NPs through the feedback between algae and the aquatic environment.