Algal Surface Research Articles

An efficient polyaluminum lanthanum silicate coagulant for phosphorus removal and algal bloom control

Due to the advantages of convenient operation and low cost, the use of coagulants is considered a promising method for algae bloom harvesting. However, large dosages, poor algal bloom control rates, and limited phosphorus removal efficiency restrict the usage of most coagulants. In this study, a novel polyaluminum lanthanum silicate (PALS) coagulant was used to remove phosphorus and control algal bloom. The results of isotherm study showed that phosphorus adsorption on PALS fitted Freundlich model, indicating chemisorption and heterogeneous multilayer adsorption were the mechanisms of phosphorus adsorption by PALS. The maximum phosphorus adsorption capacity of PALS by Langmuir model was 485.30 mg/g. According to the algal bloom control experiments, the removal of algae and phosphorus was slight at low dosages of PALS (2 mg/L and 5 mg/L). Short-term control of the algal bloom was observed within 2 days in PALS-10 group, but the bloom recovered afterward, while phosphorus and algae were almost completely removed in PALS-15 and PALS-20. When the dosage of PALS was ≤ 10 mg/L, PALS coated the algal cell surfaces and induced mild oxidative stress, showing a little damage to cell integrity. However, the PALS dose over 15 mg/L could effectively capture algal cells through charge neutralization, cause severe oxidative stress, strongly upregulate the expression of selected five genes, significantly damage cell integrity, and lead to algae lysis. These findings demonstrated that PALS is a promising coagulant for phosphorus removal and algal bloom control in eutrophic waters, and the minimum threshold of its usage was 15 mg/L.

Robust Natural Light-Absorbable and -Degradable AIE Photosensitizers for Fluorescence Labeling and Efficient Photodynamic Eradication of Algal Pollutants.

Current water pollution caused by the excessive proliferation of harmful algae urges green methods that can efficiently utilize natural light to treat algal pollution. Herein, a series of aggregation-induced emission (AIE) photosensitizers that can efficiently harness sunshine were synthesized for the environmentally friendly and biocompatible treatment of algal pollution. By tuning the number of thiophene units and the electron conjugation degree, the photosensitizers' absorptions were broadened to cover the whole visible light range. The positive charges guided photosensitizers to aggregate on algal cell surfaces, resulting in a turn-on fluorescence signal and robust reactive oxygen species generation under sunshine, thereby achieving fluorescence labeling and photodynamic eradication of algae. The eradication outcomes demonstrated that the AIE photosensitizers significantly outperformed the commercial algaecide ALG. At 20 ppm photosensitizers, 90.4% and 94.2% killing rates were achieved for C. reinhardtii and C. vulgaris, respectively, 2.8- and 3.6-fold higher than those from the same concentration of ALG. Excellent performances in inhibiting algae growth were also verified with efficiency superior to that of ALG. Importantly, the photosensitizers can self-degrade into biocompatible fragments under irradiation to avoid secondary pollution. The developed photosensitizers that possess sunshine convertibility and degradability provide an efficient tool for algal treatment, showing broad research and application prospects.

An experimental assessment of active and passive dispersal of red snow algae on the Harding Icefield, southcentral Alaska

ABSTRACT Red snow algae seasonally color glacier and alpine snow surfaces with characteristic red blooms. These blooms significantly reduce the albedo of the snow surface resulting in increased snow ablation. The global cryosphere is sensitive to the melt effect of expansive reoccurring blooms; however, the primary dispersal path by which snow algae seasonally recolonize snow surfaces is currently unresolved. Using an experimental field approach that inhibited resurfacing populations with a physical barrier, then sampled algal surface abundance the following growing season, we assessed two pathways of algal surface colonization on the Harding Icefield, Alaska. Our results provide the first experimental depiction of active resurfacing as the primary pathway of seasonal snow surface colonization by red snow algae above the equilibrium line elevation on an Alaskan glacier. Results suggest that, at the peak of the growing season, 65 percent of surface abundance was derived from actively resurfacing cells and 35 percent from passively dispersing cells.

Desorption of rare earth elements biosorbed on Euglena mutabilis suspensions and biofilms

AbstractIncreasing demand for rare earth elements (REEs) has stimulated research on novel recovery methods from sources like industrial effluents. Our recent study demonstrated that algal biofilms are good candidates for the adsorption of REEs and that the extracellular polymeric substances (EPS) within the biofilm were a key accumulator of REEs. In this work, we measured the desorption kinetics, extents, and selectivity of REEs from the algae Euglena mutabilis in suspensions and biofilms using aqueous solutions of HCl at pH between 1.5 and 4, and Na2EDTA at pH 5. We examined the potential for reusing suspended and biofilm biomass for repeated adsorption–desorption cycles. The desorption kinetics were similar for suspensions and biofilms, with equilibrium being reached within 20 min. The extent of desorption was higher in biofilms with 86% and 95% desorption, compared to suspensions which had 72% and 74% desorption using HCl and Na2EDTA, respectively. We postulate that the difference between suspensions and biofilms is attributed to the binding sites in the EPS matrix of the biofilm being more readily protonated than those at the algal cell wall surface. Heavy REEs were found to preferentially desorb at pH 4 over lighter REEs. After 3 repeated adsorption–desorption cycles, the adsorption capacity of biofilms increased by 280% and 80% using HCl and Na2EDTA, respectively, compared to an 80% decrease in biosorption capacity for the suspension. The increase in biofilm biosorption capacity was attributed to the simultaneous desorption of divalent cations alongside REEs from the EPS increasing the number of available binding sites.

Repeated release of cerium oxide nanoparticles altered algal responses: Growth, photosynthesis, and photosynthetic gene expression

The expanding production of engineered nanomaterials (ENMs) can eventually cause their increased release into and presence in aquatic ecosystems, potentially threatening the health of aquatic organisms and the stability of the ecological environment. Generally, ENMs are repeatedly released into real-world aquatic environments in relatively low concentrations, potentially affecting photosynthesis in primary producers such as algae. However, knowledge regarding the effects of repeated exposure to ENMs on algal photosynthesis is still lacking. Herein, the physiological responses of the freshwater algae Chlorella vulgaris following single and repeated exposures to cerium oxide nanoparticles (CeO2 NPs) were investigated at 10 mg/L, with a focus on photosynthesis. The results showed that repeated exposures triggered increased photosynthetic pigment contents, oxidative stress levels, decreased photosynthetic performance, and lower biomass in C. vulgaris compared to a single exposure. Photosynthesis-related genes (i.e., petA, petB, psaA, atpB, and rbcL) were found to be upregulated following repeated exposures. Particularly for petB, repeated rather than single exposure treatment significantly upregulated its expression levels by 2.92–10.24-fold compared to unexposed controls. Furthermore, increased exposure times could aggravate the interaction between CeO2 NPs and algae, elevating 8.13%, 12.13%, and 20.51% Ce distribution on the algal cell surface or intracellularly, compared to a single exposure. This study is the first to investigate the effects of ENM exposure times on algal photosynthesis, providing new insights into the assessment of the risks these materials pose to real-world aquatic environments.

Is monochloramine pre-oxidation a viable strategy for enhancing the treatment efficiency of algae-laden water with conventional drinking water treatment process?

Algal blooms worldwide pose many challenges to drinking water production. Pre-oxidation with NaClO, KMnO4, or ozone is commonly used to enhance algal removal in conventional drinking water treatment processes. However, these currently utilized oxidation methods often result in significant algal cell lysis or impede the operation of the subsequent units. Higher algal removal with pre-chlorination in algal solutions prepared with natural water, compared to those prepared with ultrapure water, has been observed. In the present studies, preliminary findings indicate that ammonium in natural water alters chlorine species to NH2Cl, leading to improved treatment efficiency. NH2Cl with 1.5–3.0 mg∙L−1 as Cl2 with an oxidation time of 3–7 h significantly enhancing algal removal by coagulation. The selective oxidation of surface-absorbed organic matter (S-AOM) by NH2Cl, followed by the subsequent peeling off of this material from the algal surface, leading to an increase in zeta potential from −20.2 mV to −3.8 mV, constitutes the primary mechanism of enhanced algal removal through coagulation. These peeled S-AOM retained their large molecular weight and acted as polymer aids. Compared with NaClO and KMnO4, NH2Cl displays the best performance in improving algal removal, avoiding cell lysis, and decreasing the potential for nitrogenous disinfection byproducts formation under the reaction conditions used in this study. Notably, in major Chinese cities, water purification plants commonly rely on suburban lakes or reservoirs as water sources, necessitating the transportation of raw water over long distances for times up to several hours. These conditions favor the implementation of NH2Cl pre-oxidation. The collective results indicate the potential of NH2Cl oxidation as a viable pretreatment strategy for algal contamination during water treatment processes.

Effects of polystyrene nanoplastics and PCB-44 exposure on growth and physiological biochemistry of Chlorella vulgaris

Both NPs and PCBs are emerging contaminants widely distributed in the environment, and it is worth exploring whether the combination of the two contaminants causes serious pollution and harm. Therefore, we studied the effects of PS-NPs and PCB-44 alone and together after 96 h and 21 d of exposure to C. pyrenoidosa. The results showed that PS-NPs and PCB-44 affected the cell cycle of C. pyrenoidosa and inhibited its normal growth. Under PS-NPs and PCB-44 stress, the relative conductivity of the algal solution increased, the hydrophobicity of the algal cell surface decreased, and the synthesis of chlorophyll a and chlorophyll b was reduced. In addition to physiological, there are biochemical effects on C. pyrenoidosa. PS-NPs and PCB-44 exposure induced oxidative stress with significant changes in the enzymatic activities of SOD and CAT together with MDA content. Moreover, the relative expression of photosynthesis-related genes (psbA, rbcL, rbcS) all responded, negatively affecting photosynthesis. In particular, significant toxic effects were observed with single exposure to PCB-44 and co-exposure to PS-NPs and PCB-44, with similar trends of effects in acute and chronic experiments. Taken together, exposure to PS-NPs and PCB-44 caused negative effects on the growth and physiological biochemistry of C. pyrenoidosa. These results provide scientific information to further explore the effects of NPs and PCBs on aquatic organisms and ecosystems.

Physicochemical surface properties of Chlorella vulgaris: a multiscale assessment, from electrokinetic and proton uptake descriptors to intermolecular adhesion forces.

Given the growing scientific and industrial interests in green microalgae, a comprehensive understanding of the forces controlling the colloidal stability of these bioparticles and their interactions with surrounding aqueous microenvironment is required. Accordingly, we addressed here the electrostatic and hydrophobic surface properties of Chlorella vulgaris from the population down to the individual cell levels. We first investigated the organisation of the electrical double layer at microalgae surfaces on the basis of electrophoresis measurements. Interpretation of the results beyond zeta-potential framework underlined the need to account for both the hydrodynamic softness of the algae cells and the heterogeneity of their interface formed with the outer electrolyte solution. We further explored the nature of the structural charge carriers at microalgae interfaces through potentiometric proton titrations. Extraction of the electrostatic descriptors of interest from such data was obscured by cell physiology processes and dependence thereof on prevailing measurement conditions, which includes light, temperature and medium salinity. As an alternative, cell electrostatics was successfully evaluated at the cellular level upon mapping the molecular interactions at stake between (positively and negatively) charged atomic force microscopy tips and algal surface via chemical force microscopy. A thorough comparison between charge-dependent tip-to-algae surface adhesion and hydrophobicity level of microalgae surface evidenced that the contribution of electrostatics to the overall interaction pattern is largest, and that the electrostatic/hydrophobic balance can be largely modulated by pH. Overall, the combination of multiscale physicochemical approaches allowed a drawing of some of the key biosurface properties that govern microalgae cell-cell and cell-surface interactions.

Removals of Some High- and Low-Density Polyethylene (HDPE and LDPE), Polypropylene (PP) and Polyvinyl Chloride (PVC) Microplastics Using Some Microalgae Types, Energy Production and Energy Recovery

Waste plastic conversion involves the treatment of plastic waste to transform in different forms of energy (heat, electricity, liquid fuels). Plastic can be converted into different forms of biofuel via thermochemical conversion methods (gasification, pyrolysis and liquefaction). Algal biomass can be converted into different forms of biofuel (crude bio-oil, bioethanol, biogas, biodiesel and bio-hydrogen) well as value added chemicals. Microalgal cells can accumulate more lipids over a shorter life cycle, they are discussed as a promising feedstock for third-generation biodiesel. The utilization of microalgae as biofuel feedstocks offers an economic, ecofriendly alternative to the use of fossil fuels the aim of microplastics (MPs) removals. Interactions between MPs and microalgal cells could enhance several important features for possible microalgal harvest and MPs accumulation. One hypothesis is microalgal biomass hypothesis can accumulate lipids and carbohydrates under microplastic stress, supporting biomass conversion into biodiesel and bioethanol. In such systems, algal cells act as bio-scavengers for MPs, binding the particles to algal surfaces or incorporating them into their cells; they are filtered from the water body and finally destroyed by further downstream processing of the polluted biomass. In this study, in order to determine biofuel (1-butanol) and methane gas [CH4(g)] production; High- and low-density polyethylene (HDPE and LDPE), polypropylene (PP), and polyvinyl chloride (PVC) MPs were removed using biomass composed of microalgae Chlamydomonas reinhardtii and Chlorella vulgaris. The algal inhibition test results proved that small groups of MPs with a size of ≈ 100 nm did not show algal inhibition. According to the algae inhibition test results, the production of 1-butanol from 100 mg/l microalgae biomass under aerobic conditions were determined as 93 ml/g for HDPE, 236 ml/g for LDPE, 387 ml/g for PP and 459 ml/g for PVC. According to the algae inhibition test results, the production of CH4(g) from 400 mg/l microalgae biomass under anaerobic conditions were measured as 452 ml/g for HDPE, 510 ml/g for LDPE, 529 ml/g for PP and 541 ml/g for PVC. 91.26%, 94.52%, 98.34% and 96.17% energy recoveries were measured for HDPE, LDPE, PP and PVC MPs, respectively, after microalgae biomass experiments, at pH=7.0 and at 35oC. Maximum 98.34% energy recovery was obtained for PP MPs after microalgae biomass experiments, at pH=7.0 and at 35oC.

Metabolomics and Microbiomics Insights into Differential Surface Fouling of Three Macroalgal Species of Fucus (Fucales, Phaeophyceae) That Co-Exist in the German Baltic Sea.

The brown algal genus Fucus provides essential ecosystem services crucial for marine environments. Macroalgae (seaweeds) release dissolved organic matter, hence, are under strong settlement pressure from micro- and macrofoulers. Seaweeds are able to control surface epibionts directly by releasing antimicrobial compounds onto their surfaces, and indirectly by recruiting beneficial microorganisms that produce antimicrobial/antifouling metabolites. In the Kiel Fjord, in the German Baltic Sea, three distinct Fucus species coexist: F. vesiculosus, F. serratus, and F. distichus subsp. evanescens. Despite sharing the same habitat, they show varying fouling levels; F. distichus subsp. evanescens is the least fouled, while F. vesiculosus is the most fouled. The present study explored the surface metabolomes and epiphytic microbiota of these three Fucus spp., aiming to uncover the factors that contribute to the differences in the fouling intensity on their surfaces. Towards this aim, algal surface metabolomes were analyzed using comparative untargeted LC-MS/MS-based metabolomics, to identify the marker metabolites influencing surface fouling. Their epiphytic microbial communities were also comparatively characterized using high-throughput amplicon sequencing, to pinpoint the differences in the surface microbiomes of the algae. Our results show that the surface of the least fouling species, F. distichus subsp. evanescens, is enriched with bioactive compounds, such as betaine lipids MGTA, 4-pyridoxic acid, and ulvaline, which are absent from the other species. Additionally, it exhibits a high abundance of the fungal genera Mucor and Alternaria, along with the bacterial genus Yoonia-Loktanella. These taxa are known for producing antimicrobial/antifouling compounds, suggesting their potential role in the observed fouling resistance on the surface of the F. distichus subsp. evanescens compared to F. serratus and F. vesiculosus. These findings provide valuable clues on the differential surface fouling intensity of Fucus spp., and their importance in marine chemical defense and fouling dynamics.

Characterizing photochemical production carboxyl content of dissolved organic matters using absorbance spectroscopy combined with FT-ICR MS

Irradiation can significantly impact the structure, reactivity and environmental behavior of dissolved organic matter (DOM). The extent of these processes remains to be ascertained in more detail but the heterogeneity and site-specificity of DOM, and the lack of methods to characterize DOM at its environmentally-relevant concentrations make it a challenge. In this study, the differences of DOM response to photodegradation in four typical origins (i.e., surface water, sediment and intracellular and extracellular algal DOM) were tracked on the molecular-level using Fourier Transform Ion Cyclotron Resonance Mass Spectrometry (FT-ICR MS). Changes of the carboxyl and phenolic DOM moieties induced by irradiation were quantified by spectroscopic titrations, and the mechanism of functional groups affecting the changes of specific molecular composition was qualitatively proposed. The results demonstrated that intracellular algal organic matter (I-DOM) was most susceptible to photodegradation (ca. 63% DOM loss), then came extracellular algal organic matter (E-DOM) and surface water DOM (W-DOM) (ca. 15% DOM loss). Sediment DOM (S-DOM) was most resistant to irradiation, with a very small level of its mineralization. Lipids, lignin-like compounds and tannin-like compounds in I-DOM and E-DOM were relatively photo-labile. The photodegradation of lipids was related to the decarboxylation of carboxyl functional groups, while the photodegradation of tannin-like compounds was related to the rupture of phenolic functional groups. In comparison, the molecular composition of W-DOM and S-DOM was less affected by irradiation, which was also reflected in the fact that the carboxyl and phenolic functional groups were highly photo-resistant. This study showed that the photoactivity of DOM in surface water was closely related to the abundance of algae, so controlling the excessive reproduction of algae may have a positive effect on stability of quality and quantity of organic matter in surface water.

Effect of lead ions on biochemical behavior of Cladophora glomerata in sterilized and non-sterilized media.

Freshwater ecosystems are under peril globally due to anthropogenic influences, most notably metals. The present study aimed to evaluate the morphological and biochemical responses of Cladophora glomerata obtained from a freshwater stream to various lead concentrations (0.0, 7.5, 15, 30, and 60 mg/L Pb2+) in sterilized and non-sterilized media. Pigments, proline, malondialdehyde (MDA), total phenolic compounds (TPC), hydrogen peroxide, and protein content of the green alga were determined in response to various growing conditions. Pb2+ stress had a detrimental effect not only on biochemical components of C. glomerata but also on the algal cell's shape and surface structure. High Pb2+ concentrations significantly decreased chlorophyll-a (from 1350 μg/g in non-sterilized and 1340 μg/g in sterilized media for the control group to 1067 μg/g in non-sterilized and 1049 μg/g in sterile media at 60 mg/L Pb2+) and protein contents (from 34.47 mg/g for the sterilized and 35.89 mg/g for non-sterilized of the control to 24.82 mg/g for the sterilized and 26.18 mg/g for the non-sterilized at 60 mg/L Pb2+) of algal biomass but increased the concentrations of stress compounds (e.g., MDA, proline, and TPC). Variation in the macroalgal biomass composition was also indicated by FTIR analysis based on interactions between amino, amide, and anionic surface groups on the algal biomass and Pb2+ ions. Morphological and biochemical responses of C. glomerata reveal that non-sterile conditions encouraged the proliferation of this macroalga under Pb2+ exposure.

Effective and sustainable bioremediation of molybdenum pollutants from wastewaters by potential microalgae

Due to industrialization and growing population have greatly affected the quality of natural water resources globally. Molybdenum is a harmful metal that can cause serious health issues when exposed to >10 ppm levels. Several industries routinely discharged it, hence posing the environmental problems. For discharged industrial effluents, there are not any environmentally friendly and sustainable treatment method have developed for removing molybdenum hazards. The objective of this study was to design a green, sustainable approach for removing the molybdenum pollutant and to offset the treatment cost by obtaining values from microalgal by-products. Chlorella sorokiniana TU5 and Picochlorum oklahomensis, two fast-growing microalgal strains, were used for molybdenum treatment. The maximum removal efficiency was 115.65 mg L−1 with biomass and lipid yield of 2.35 g L−1 and 579.3 mg L−1, respectively, after 14 days of growth and further exposure to molybdenum pollutant. The molybdenum removal capacity was further increased by optimizing crucial factors, pH and temperature before removing biomass from the aqueous phase. Zeta potential study helped to determine the pH range that appropriately facilitate the strongest possible ionic bonds, leading to the enhanced molybdenum adsorption. In order to verify molybdenum adsorption and comprehend the dominating and quantitative interactions, FTIR was carried out to analyze the reactive groups in the algal cell surface. The current work analyses to control external parameters for improving the adsorption efficiency during harvesting of microalgal biomass, which efficiently improved the removal of molybdenum (V) from the liquid phase. The proposed technique aims to improve the bioremediation efficiency of molybdenum and other inorganic contaminants at an industrial scale by using microalgal treatment.

Aging process does not necessarily enhance the toxicity of polystyrene microplastics to Microcystis aeruginosa

Microplastic (MP) pollution in aquatic systems has attracted increasing attention in recent years. MPs will inevitably encounter aging process in the environment. However, research on the effects of aged MPs on freshwater ecosystems remains limited. This study compared the properties of pristine and aged polystyrene (PS) MPs of different sizes (20 nm, 200 nm, 2000 nm) and determined the effects of aging on the toxicity of PS MPs to typical freshwater cyanobacteria, Microcystis aeruginosa. Aging process induced significant changes to the properties of the MPs, especially their microstructures and surface functional groups. Aging process also influenced zeta potential, which could further affect stability and toxicity of PS MPs. After 96 h exposure, increase of algal growth and photosynthetic activity was observed in the treatment of pristine 200 nm, aged 20 nm and aged 200 nm PS MPs. In addition, pristine 20 nm, pristine 200 nm, pristine 2000 nm, aged 20 nm and aged 200 nm PS MPs were adsorbed on algal cell surface, which could influence the cell permeability. Pristine PS MPs promoted microcystin synthesis and release, which could do harm to drinking water safety and freshwater ecosystems. However, there was no significant increase in aged PS MPs treatments. Furthermore, the increased 13C content of algal cells in all pristine PS MPs treatments indicated that M. aeruginosa assimilated more CO2 and generate more energy to resist the stress of pristine PS MPs when compared with aged PS MPs. These results indicate that aging process did not necessarily enhance the toxicity and biological risk of PS MPs to freshwater ecosystems. Findings of this study fill the knowledge gap in understanding the effects and risks of aged MPs on freshwater ecosystems.

Multilayer adsorption of lead (Pb) and fulvic acid by Chlorella pyrenoidosa: Mechanism and impact of environmental factors

When the multilayer adsorption of lead (Pb) and fulvic acid (FA) occurs on algal surface, the adsorption capacity of Pb on the algae will increase dramatically, thus increasing the environmental risk of Pb. However, the corresponding mechanism and the influence of environmental factors on the multilayer adsorption remain unclear. Here, microscopic observation methods and batch adsorption experiments were exactly designed to investigate the adsorption behavior of multilayer adsorption of Pb and FA on algal surface. The results of Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) revealed that carboxyl groups were the major functional groups responsible for the binding of Pb ions in multilayer adsorption, and its number was more than that in monolayer adsorption. The solution pH, with an optimal pH of 7, was a critical factor influencing the occurrence of multilayer adsorption because it influences the protonation of the involved functional groups and determines the concentration of Pb2+ and Pb-FA in the solution. Increasing the temperature was beneficial for multilayer adsorption, with ΔH for Pb and FA varied from +17.12 to +47.68 kJ/mol and +16.19 to +57.74 kJ/mol, respectively. The multilayer adsorption of Pb and FA onto algal surface also followed the pseudo-second order kinetic model, but was extremely slower than the monolayer adsorption of Pb and FA by 30 times and 15 orders of magnitude, respectively. Therefore, the adsorption of Pb and FA in the ternary system had a different adsorption behavior than that in the binary system, which verified the presence of multilayer adsorption of Pb and FA and further support the multilayer adsorption mechanism. This work is important to provide data support for water ecological risk prevention and control of heavy metals.

Recovery of Water Quality and Detection of Algal Blooms in Lake Villarrica through Landsat Satellite Images and Monitoring Data

Phytoplankton is considered a strong predictor of the environmental quality of lakes, while Chlorophyll-a is an indicator of primary productivity. In this study, 25 LANDSAT images covering the 2014–2021 period were used to predict Chlorophyll-a in the Villarrica lacustrine system. A Chlorophyll-a recovery algorithm was calculated using two spectral indices (FAI and SABI). The indices that presented the best statistical indicators were the floating algal index (R2 = 0.87) and surface algal bloom index (R2 = 0.59). A multiparametric linear model for Chlorophyll-a estimation was constructed with the indices. Statistical indicators were used to validate the multiple linear regression model used to predict Chlorophyll-a by means of spectral indices, with the following results: a MBE of −0.136 μ, RMSE of 0.055 μ, and NRMSE of 0.019%. All results revealed the strength of the model. It is necessary to raise awareness among the population that carries out activities around the lake in order for them to take policy actions related to water resources in this Chilean lake. Furthermore, it is important to note that this study is the first to address the detection of algal blooms in this Chilean lake through remote sensing.

Algicidal substances of Brevibacillus laterosporus and their effect on red tide organisms

Herein, the algicidal effects of Brevibacillus laterosporus on typical red tide organisms were investigated. Through comparative analysis of the fermentation solution, sterile filtrate and bacterial body, it was found that this strain mainly exerts its algicidal function by secreting algicidal substances. In this paper, we established a method for extracting the algicidal substances of B. laterosporus and systematically investigated their features and effect on Heterosigma akashiwo. The results showed that the algicidal substances are a mixture of compounds all with molecular weights less than 3500 Da, with those below 100 Da producing 45% of the algicidal effect; these are more polar and best extracted with methanol. The algicidal substances are stable over a range of temperatures (-80.0 to 70.0°C) and pH values (4.0-8.0). The algicidal substances caused most H. akashiwo cells to rupture within 24 h. In the remaining cells, the algicidal substances activated the antioxidant system and reduced their metabolic activity, leading to apoptosis, as observed by cell crumbling and a reduction in membrane potential. The responses of different algal cell surface structures to the algicidal substances were also compared and analysed. It was concluded that these algicidal substances can act on the cell membrane and change its permeability, allowing entry of the algicidal substances to produce an algicidal effect.

Factors affecting the toxicity and oxidative stress of layered double hydroxide-based nanomaterials in freshwater algae

Layered double hydroxide (LDH) nanomaterials are utilized extensively in numerous fields because of their distinctive structural properties. It is critical to understand the environmental behavior and toxicological effects of LDHs to address potential concerns caused by their release into the environment. In this work, the toxicological effects of two typical LDHs (Mg-Al-LDH and Zn-Al-LDH) on freshwater green algae (Scenedesmus obliquus) and the main affecting factors were examined. The Zn-Al-LDH exhibited a stronger growth inhibition toxicity than the Mg-Al-LDH in terms of median effect concentration. This toxicity difference was connected to the stability of particle dispersion in water and the metallic composition of LDHs. The contribution of the dissolved metal ions to the overall toxicity of the LDHs was lower than that of their particulate forms. Moreover, the joint toxic action of different dissolved metal ions in each LDH belonged to additive effects. The Mg-Al-LDH induced a stronger oxidative stress effect in algal cells than the Zn-Al-LDH, and mitochondrion was the main site of LDH-induced production of reactive oxygen species. Scanning electron microscope observation indicated that both LDHs caused severe damage to the algal cell surface. At environmentally relevant concentrations, the LDHs exhibited joint toxic actions with two co-occurring contaminants (oxytetracycline and nano-titanium dioxide) on S. obliquus in an additive manner mainly. These findings emphasize the impacts of the intrinsic nature of LDHs, the aqueous stability of LDHs, and other environmental contaminants on their ecotoxicological effects.

Evaluation of Cd2+ stress on Synechocystis sp. PCC6803 based on single-cell elemental accumulation and algal toxicological response

With the development of single cell analysis techniques, the concept of precision toxicology has been proposed in recent years. Due to the heterogeneity of cells, we need to perform toxicological assessments on individual cells. Microalgae, one kind of important primary producers, play as a major pathway by which heavy metals enter the food chain and thus accumulate/transfer to higher trophic levels. Herein, the biosorption of Cd (Ex-Cd) and bioaccumulation of Cd (In-Cd) for Synechocystis sp. PCC 6803 were investigated by online 3D droplet microfluidic device combined with inductively coupled plasma mass spectrometry detection. Meanwhile, the algal toxicological responses of the algae cell to Cd2+ exposure under different concentration (50, 100, and 150 μg L − 1) and time (15 min, 24, 48 and 96 h) were studied. Combining single-cell analysis with toxicological indicators, the toxicity mechanism of Cd2+to algal was discussed. The single cell analysis results revealed heterogeneity in cellular uptake of Cd2+. The proportion of Cd-containing cells and Cd content in single algal cells all reached the maximum at 24 h. The uptake of Cd2+ occurred within 15 min under all tested exposure concentrations and a large part of Cd2+ were adsorbed on the algal cells surface. The Pearson correlation analysis showed that cell density, chlorophyll a and carotenoids were significantly negatively correlated with Cd accumulation, whereas ROS level and SOD activity were significantly positively correlated with Cd accumulation. It suggested that Cd2+accumulated intracellular would show toxic effects on the algal cells and oxidative stress is the main mechanism of Cd toxicity to algal cells. This work promotes our understanding of the toxicological responses of microalgae under Cd stress at single cells level.

Characterization of a bloom-associated alphaproteobacterial lineage, ‘Candidatus Phycosocius’: insights into freshwater algal-bacterial interactions

Marine bacterial lineages associated with algal blooms, such as the Roseobacter clade, have been well characterized in ecological and genomic contexts, yet such lineages have rarely been explored in freshwater blooms. This study performed phenotypic and genomic analyses of an alphaproteobacterial lineage ‘Candidatus Phycosocius’ (denoted the CaP clade), one of the few lineages ubiquitously associated with freshwater algal blooms, and described a novel species: ‘Ca. Phycosocius spiralis.’ Phylogenomic analyses indicated that the CaP clade is a deeply branching lineage in the Caulobacterales. Pangenome analyses revealed characteristic features of the CaP clade: aerobic anoxygenic photosynthesis and essential vitamin B auxotrophy. Genome size varies widely among members of the CaP clade (2.5–3.7 Mb), likely a result of independent genome reductions at each lineage. This includes a loss of tight adherence pilus genes (tad) in ‘Ca. P. spiralis’ that may reflect its adoption of a unique spiral cell shape and corkscrew-like burrowing activity at the algal surface. Notably, quorum sensing (QS) proteins showed incongruent phylogenies, suggesting that horizontal transfers of QS genes and QS-involved interactions with specific algal partners might drive CaP clade diversification. This study elucidates the ecophysiology and evolution of proteobacteria associated with freshwater algal blooms.