Ecotoxicity of Diazinon and Atrazine Mixtures after Ozonation Catalyzed by Na+ and Fe2+ Exchanged Montmorillonites on Lemna minor.

The toxicity of two pesticides, diazinon (DAZ) and atrazine (ATR), before and after montmorillonite-catalyzed ozonation was comparatively investigated on the duckweed Lemna minor. The results allowed demonstrating the role of clay-containing media in the evolution in time of pesticide negative impact on L. minor plants. Pesticides conversion exceeded 94% after 30 min of ozonation in the presence of both Na+ and Fe2+ exchanged montmorillonites. Toxicity testing using L. minor permitted us to evaluate the change in pesticide ecotoxicity. The plant growth inhibition involved excessive oxidative stress depending on the pesticide concentration, molecular structure, and degradation degree. Pesticide adsorption and/or conversion by ozonation on clay surfaces significantly reduced the toxicity towards L. minor plants, more particularly in the presence of Fe(II)-exchanged montmorillonite. The results showed a strong correlation between the pesticide toxicity towards L. minor and the level of reactive oxygen species, which was found to depend on the catalytic activity of the clay minerals, pesticide exposure time to ozone, and formation of harmful derivatives. These findings open promising prospects for developing a method to monitor pesticide ecotoxicity according to clay-containing host-media and exposure time to ambient factors.

Role of Silica on Clay-Catalyzed Ozonation for Total Mineralization of Bisphenol-A.

Catalytic ozonation for the total mineralization of bisphenol-A (BPA) from aqueous solution was investigated in the presence of various silica-based catalysts such as mesoporous silica, acid-activated bentonite (HMt) and montmorillonite-rich materials (Mt) ion-exchanged with Na+ and Fe2+ cations (NaMt and Fe(II)Mt). The effects of the catalyst surface were studied by correlating the hydrophilic character and catalyst dispersion in the aqueous media to the silica content and BPA conversion. To the best of our knowledge, this approach has barely been tackled so far. Acid-activated and iron-free clay catalysts produced complete BPA degradation in short ozonation times. The catalytic activity was found to strongly depend on the hydrophilic character, which, in turn, depends on the Si content. Catalyst interactions with water and BPA appear to promote hydrophobic adsorption in high Si catalysts. These findings are of great importance because they allow tailoring silica-containing catalyst properties for specific features of the waters to be treated.

Clay-Catalyzed Ozonation of Organic Pollutants in Water and Toxicity on Lemna minor: Effects of Molecular Structure and Interactions.

The use of clays as adsorbents and catalysts in the ozonation of organic pollutants (Atrazine, bis-Phenol A, Diazinon, and Diclofenac sodium) allowed simulating their natural oxidative degradation in clay soils and to evaluate the ecotoxicity of mixtures partially oxidized on the species Lemna minor, a biodiversity representative of plants in the aquatic environment. Kinetic data showed that the adsorption of organic pollutants on clay particles obeys the pseudo-second-order model, while the adsorption isotherms satisfactorily fit the Langmuir model. Adsorption reduces the dispersion of the organic pollutant in the environment and prolongs its persistence and its natural degradation probability. Measurements of the Zeta potential and particle size as a function of pH demonstrate that the catalytic activity of clay depends on its cation, its silica/alumina ratio, and therefore on its permanent and temporary ion exchange capacities. These factors seem to govern its delamination and dispersion in aqueous media, its hydrophilic-hydrophobic character, and its porosity. Tests conducted on Lemna minor in contact with ozonation mixtures revealed that the toxicity could be due to pH decrease and to the toxicity of the intermediates yielded. Ecotoxicity would depend on the structure of the organic molecules, the chemical composition of the clay surface and ozonation time, which determines the oxidation progress. These results are of great importance for further research because they allow concluding that the negative impact of the persistence of an organic molecule in clay-containing media depends on the type and composition of the very clay mineral.

Cadmium accumulation and toxicity affect the extracytoplasmic polyphosphate level in Chlamydomonas reinhardtii.

Cadmium is a non-essential metal and highly toxic for biological functions. Depending on the dose of Cd2+, the biochemical response will differ. In this study, we investigated the level of extracytoplasmic polyphosphate (polyP) when Chlamydomonas reinhardtii was exposed to the effect of CdCl2. When compared to control cells, Cd2+-treated cells to 400-600 µM showed a decrease in the growth rate from 0.78 to 0.38 d-1 for the strain CC-125, and a decrease from 0.81 to 0.32-0.35 d-1 for CC-503. This indicated a strong toxicity effect on the population growth of cells during 72 h. In addition, the results demonstrated the decrease in the synthesis and/or the degradation of polyP that was correlated with the accumulation of Cd2+ in both algal strains. Furthermore, the level of polyP decreased in relation to the decrease of FV/FM value. The toxicity of Cd2+ induced a high level of cell necrosis for CC-503, and the level of polyP could not be recovered at 72 h. In response to the toxic effects of Cd2+, the observed formation of palmelloid colonies by CC-125 cells was correlated with the recovery of the polyP level. Nevertheless, both algal strains were able to accumulate significant amount of Cd2+ in their biomass. Therefore, our study demonstrated a distinct impact of Cd2+ on the metabolism of polyP (synthesis and/or degradation), which was dependent on the concentration of CdCl2 and the Chlamydomonas strain. Based on this study, the level of polyP can be used as a biomarker of Cd2+ toxicity at 24-48 h, even with the cell wall-deficient strain CC-503.

A flavin binding cryptochrome photoreceptor responds to both blue and red light in Chlamydomonas reinhardtii.

Cryptochromes are flavoproteins that act as sensory blue light receptors in insects, plants, fungi, and bacteria. We have investigated a cryptochrome from the green alga Chlamydomonas reinhardtii with sequence homology to animal cryptochromes and (6-4) photolyases. In response to blue and red light exposure, this animal-like cryptochrome (aCRY) alters the light-dependent expression of various genes encoding proteins involved in chlorophyll and carotenoid biosynthesis, light-harvesting complexes, nitrogen metabolism, cell cycle control, and the circadian clock. Additionally, exposure to yellow but not far-red light leads to comparable increases in the expression of specific genes; this expression is significantly reduced in an acry insertional mutant. These in vivo effects are congruent with in vitro data showing that blue, yellow, and red light, but not far-red light, are absorbed by the neutral radical state of flavin in aCRY. The aCRY neutral radical is formed following blue light absorption of the oxidized flavin. Red illumination leads to conversion to the fully reduced state. Our data suggest that aCRY is a functionally important blue and red light-activated flavoprotein. The broad spectral response implies that the neutral radical state functions as a dark form in aCRY and expands the paradigm of flavoproteins and cryptochromes as blue light sensors to include other light qualities.

Effects of superparamagnetic iron oxide nanoparticles on photosynthesis and growth of the aquatic plant Lemna gibba.

Toxicity of superparamagnetic iron oxide nanoparticles (SPION) was investigated in Lemna gibba plants exposed for 7 days to Fe3O4 (SPION-1), Co0.2Zn0.8Fe2O4 (SPION-2), or Co0.5Zn0.5Fe2O4 (SPION-3) at 0, 12.5, 25, 50, 100, 200 or 400 µg mL(-1). At < 400 µg mL(-1) of SPION exposure, toxicity was indicated by decrease of chlorophyll content, deterioration of photosystem II (PSII) functions, strong production of reactive oxygen species (ROS), and inhibition of growth rate based on fresh weight (52-59 %) or frond number (32-49 %). The performance index of PSII activity was the most sensitive biomarker of PSII functions and decreased by 83, 86, and 79 % for SPION-1, SPION-2, and SPION-3, respectively. According to the change of these biomarkers, the exposure of SPION suspensions to L. gibba caused several alterations to the entire plant cellular system, which may come from both the uptake of nanoparticles and metal ions in the soluble fraction. Our results, based on the change of several biomarkers, showed that these SPION have a complex toxic mode of action on the entire plant system and therefore affects its viability. Therefore, the plant model L. gibba was shown to be a sensitive bioindicator of SPION cellular toxicity and thus can be used in the development of a laboratory bioassay toxicity testing.

Locomotion behavior testing as a complementary tool in Collembola avoidance assays with neurotoxic insecticides.

This study aimed (1) to assess the ability of collembolans Folsomia candida to avoid soils contaminated with three seed dressing insecticides imidacloprid, clothianidin, and fipronil; (2) to assess the effects of the insecticides on collembolans' locomotion behavior; (3) to check if changes in the locomotion behavior would explain the avoidance/preference responses; and (4) to evaluate the possibility to use locomotion behavior as toxicity biomarker of the tested insecticides. Avoidance and locomotion behavior assays with collembolans F. candida were performed with commercial seed dressing formulations of three insecticides (imidacloprid, clothianidin, and fipronil). Results showed no avoidance behavior at any concentration, while a "preference" was observed with increasing concentrations of the three tested insecticides. Significant reductions in the locomotion of exposed collembolans were observed at ≥ 1 mg kg-1 for imidacloprid (18-38%) and fipronil (29-58%) and ≥ 4 mg kg-1 for clothianidin (10-47%). At the higher insecticide concentrations, the collembolans had their trajectories restricted to smaller areas, with a tendency for circular movements. Our results confirm that the "preference" for contaminated soils with neurotoxic substances is likely due to locomotion inhibition impairing the ability of organisms to escape. This effect highlights that only avoidance assays may be not sufficient to assure the safety of some substances and confirm the potential of locomotion behavior as a sensitive toxicity biomarker for neurotoxic insecticides.

Polyclonal antibodies against the TLA1 protein also recognize with high specificity the D2 reaction center protein of PSII in the green alga Chlamydomonas reinhardtii.

The Chlamydomonas reinhardtii DNA-insertional transformant truncated light-harvesting antenna 1 (tla1) mutant, helped identify the novel TLA1 gene (GenBank Accession # AF534570-71) as an important genetic determinant in the chlorophyll antenna size of photosynthesis. Down-regulation in the amount of the TLA1 23 kDa protein in the cell resulted in smaller chlorophyll antenna size for both photosystems (in Tetali et al. Planta 225:813-829, 2007). Specific polyclonal antibodies, raised against the recombinant TLA1 protein, showed a cross-reaction with the predicted 23 kDa TLA1 protein in C. reinhardtii protein extracts, but also showed a strong cross-reaction with a protein band migrating to 28.5 kDa. Questions of polymorphism, or posttranslational modification of the TLA1 protein were raised as a result of the unexpected 28.5 kDa cross-reaction. Work in this paper aimed to elucidate the nature of the unexpected 28.5 kDa cross-reaction, as this was deemed to be important in terms of the functional role of the TLA1 protein in the regulation of the chlorophyll antenna size of photosynthesis. Immuno-precipitation of the 28.5 kDa protein, followed by LC-mass spectrometry, showed amino acid sequences ascribed to the psbD/D2 reaction center protein of PSII. The common antigenic determinant between TLA1 and D2 was shown to be a stretch of nine conserved amino acids V-F-L(V)LP-GNAL in the C-terminus of the two proteins, constituting a high antigenicity "GNAL" domain. Antibodies raised against the TLA1 protein containing this domain recognized both the TLA1 and the D2 protein. Conversely, antibodies raised against the TLA1 protein minus the GNAL domain specifically recognized the 23 kDa TLA1 protein and failed to recognize the 28.5 kDa D2 protein. D2 antibodies raised against an oligopeptide containing this domain also cross-reacted with the TLA1 protein. It is concluded that the 28.5 kDa cross-reaction of C. reinhardtii protein extracts with antiTLA1 antibodies is due to antibody affinity for the GNAL domain of the D2 protein and has no bearing on the identity or function of the TLA1 protein.

Insight into natural medium remediation through ecotoxicity correlation with clay catalyst selectivity in organic molecule ozonation.

The oxidative degradation of diazinon (DAZ) and diclofenac sodium (DCF) in aqueous media was comparatively investigated and correlated with the mortality of Artemia salina in the presence of clay catalysts. For this purpose, montmorillonites (Mt) exchanged with Na+ and Fe2+ cations (NaMt and Fe(II)Mt), acid activated bentonites and hydrotalcite were used as clay catalysts. Surface interaction and adsorption on the clay surface were found to govern the catalyst dispersion in aqueous media and both activity and selectivity in ozonation. These catalysts' features were correlated with the ecotoxicity of ozonised reaction mixtures as expressed in terms of mortality rates of Artemia salina. DAZ and DCF display specific intrinsic ecotoxicity that evolves differently during ozonation according to the catalyst. The ecotoxicity was found to strongly depend on the distribution of the ozonation intermediates, which, in turn, was narrowly correlated with the acid-base properties of the catalyst surface. These valuable findings allow the prediction of the behaviour of the clay-containing media in natural remediation.

Toxic Responses of Palladium Accumulation in Duckweed (Lemna minor): Determination of Biomarkers.

Palladium (Pd) is a trace metal of the platinum group elements, representing an emerging contaminant for the environment. It is of great interest to characterize the bioaccumulation and toxicity of Pd to improve our toxicological knowledge for this contaminant. Under standardized toxicity testing conditions, we analyzed Pd accumulation and toxicity effects on the duckweed Lemna minor exposed to nominal concentrations from 2 to 50 µM. The inhibitory effect was significant (p < 0.05) from 8 µM of Pd, starting with 9.5% of growth inhibition and a decrease of 1 cm for the root size. Under 12.5 µM of Pd, the bioaccumulated Pd of 63.93 µg/g fresh weight inhibited plant growth by 37.4%, which was caused by a strong oxidative stress in the cytosol and organelles containing DNA. Under 25 and 50 µM of Pd, bioaccumulated Pd was able to deteriorate the entire plant physiology including chlorophyll synthesis, the photosystem II antenna complex, and the photochemical reactions of photosynthesis. In fact, plants treated with 50 µM Pd accumulated Pd up to 255.95 µg/g fresh weight, causing a strong decrease in total biomass and root elongation process. Therefore, we showed several growth, physiological, and biochemical alterations which were correlated with the bioaccumulation of Pd. These alterations constituted toxicity biomarkers of Pd with different lowest-observed-effect dose, following this order: root size = growth inhibition < catalase activity = carotenoid content = reactive oxygen species production = total thiols < chlorophyll a/b = variable fluorescence to maximal fluorescence intensity ratio = absorbed-light energy transfer from the chlorophyll a antenna to the photosystem II reaction center = performance index of photosystem II activity < VJ . Therefore, the present study provides insight into the toxicity mechanism of Pd in L. minor plants under standardized testing conditions. Environ Toxicol Chem 2021;40:1630-1638. © 2021 SETAC.

Interaction Effect of EDTA, Salinity, and Oxide Nanoparticles on Alga Chlamydomonas reinhardtii and Chlamydomonas euryale.

The interaction effects of organic ligand ethylene diamine tetra-acetic acid (EDTA) and oxide nanoparticles (magnetite Fe3O4-NPs and copper CuO-NPs) were investigated during a 72 h period on two green algal species-Chlamydomonas reinhardtii under freshwater conditions and Chlamydomonas euryale under saltwater conditions. Fe3O4-NPs had larger agglomerates and very low solubility. CuO-NPs, having smaller agglomerates and higher solubility, were more toxic than Fe3O4-NPs in freshwater conditions for similar mass-based concentrations, especially at 72 h under 100 mg L-1. Furthermore, the effect of EDTA increased nanoparticle solubility, and the salinity caused a decrease in their solubility. Our results on C. euryale showed that the increase in salinity to 32 g L-1 caused the formation of larger nanoparticle agglomerates, leading to a decrease in the toxicity impact on algal cells. In addition, EDTA treatments induced a toxicity effect on both freshwater and saltwater Chlamydomonas species, by altering the nutrient uptake of algal cells. However, C. euryale was more resistant to EDTA toxicity than C. reinhardtii. Moreover, nanoparticle treatments caused a reduction in EDTA toxicity, especially for CuO-NPs. Therefore, the toxicity impact caused by these environmental factors should be considered in risk assessment for metallic nanoparticles.

Phylogenomic analysis of the Chlamydomonas genome unmasks proteins potentially involved in photosynthetic function and regulation.

Chlamydomonas reinhardtii, a unicellular green alga, has been exploited as a reference organism for identifying proteins and activities associated with the photosynthetic apparatus and the functioning of chloroplasts. Recently, the full genome sequence of Chlamydomonas was generated and a set of gene models, representing all genes on the genome, was developed. Using these gene models, and gene models developed for the genomes of other organisms, a phylogenomic, comparative analysis was performed to identify proteins encoded on the Chlamydomonas genome which were likely involved in chloroplast functions (or specifically associated with the green algal lineage); this set of proteins has been designated the GreenCut. Further analyses of those GreenCut proteins with uncharacterized functions and the generation of mutant strains aberrant for these proteins are beginning to unmask new layers of functionality/regulation that are integrated into the workings of the photosynthetic apparatus.

Effect of aluminum on cellular division and photosynthetic electron transport in Euglena gracilis and Chlamydomonas acidophila.

The present study investigated aluminum's effect on cellular division and the photosynthetic processes in Euglena gracilis and Chlamydomonas acidophila at pH 3.0, at which Al is present mostly as Al(3+), AlSO(4) (+), and Al(SO(4))(2) (-). These algal species were exposed to 100, 188, and 740 microM Al, and after 24 h cell-bound Al was significantly different from control only for the highest concentration tested. However, very different effects of Al on algal cellular division, biomass per cell, and photosynthetic activity were found. Aluminum stimulated cell division but decreased at some level biomass per cell in C. acidophila. Primary photochemistry of photosynthesis, as Photosystem II quantum yield, and energy dissipation via nonphotochemical activity were slightly affected. However, for E. gracilis, under the same conditions, Al did not show a stimulating effect on cellular division or photosynthetic activity. Primary photochemical activity was diminished, and energy dissipation via nonphotochemical pathways was strongly increased. Therefore, when Al is highly available in aquatic ecosystems, these effects may indicate very different response mechanisms that are dependent on algal species.

Functionalized Glutathione on Chitosan-Genipin Cross-Linked Beads Used for the Removal of Trace Metals from Water.

Functionalized glutathione on chitosan-genipin cross-linked beads (CS-GG) was synthesized and tested as an adsorbent for the removal of Fe(II) and Cu(II) from aqueous solution. The beads were characterized by several techniques, including Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), CNS elementary analysis, scanning electron microscopy (SEM), and atomic force microscopy (AFM). The effect of several parameters such as the pH, the temperature, and the contact time was tested to optimize the condition for the adsorption reaction. The beads were incubated in aqueous solutions contaminated with different concentrations of Fe(II) and Cu(II) (under the range concentration from 10 to 400 mg·L-1), and the adsorption capacity was evaluated by inductively coupled plasma optical emission spectrometry (ICP-OES). The adsorption equilibrium was reached after 120 min of incubation under optimal pH 5 for Fe(II) and after 180 min under optimal pH 6 for Cu(II). According to the Langmuir isotherm, the maximum adsorption capacities (q max) for Fe(II) and Cu(II) were 208 mg·g-1 and 217 mg·g-1, respectively. Our results showed that the adsorption efficiency of both metals on CS-GG beads was correlated with the degree of temperature. In addition, the adsorption reaction was spontaneous and endothermic, indicated by the positive values of ΔG 0 and ΔH 0. Therefore, the present study demonstrated that the new synthesized CS-GG beads had a strong adsorption capacity for Fe(II) and Cu(II) and were efficient to remove these trace metals from aqueous solution.

Antisense inhibition of the PsbX protein affects PSII integrity in the higher plant Arabidopsis thaliana.

PSII, the oxygen-evolving complex of photosynthetic organisms, contains an intriguingly large number of low molecular weight proteins. PsbX, one of these proteins, is ubiquitous in PSII complexes of cyanobacteria and plants. In previous studies, deletion of the PsbX protein in cyanobacteria has not resulted in clear phenotypic changes. Here we report the construction of an antisense (AS-PsbX) line in Arabidopsis thaliana with <10% of wild-type PsbX levels. AS-PsbX plants are capable of photoautotrophic growth, but biochemical, biophysical and immunological evidence demonstrates that reduction of PsbX contents leads to reduced levels of functional assembled PSII core complexes, while the light-harvesting antennae are not affected. In addition, levels of phosphorylation of the core proteins D1, D2 and CP43 are severely reduced in the antisense plants relative to their wild-type counterparts. We conclude that PsbX is important for accumulation of functional PSII.

Validation of photosynthetic-fluorescence parameters as biomarkers for isoproturon toxic effect on alga Scenedesmus obliquus.

Photosynthetic-fluorescence parameters were investigated to be used as valid biomarkers of toxicity when alga Scenedesmus obliquus was exposed to isoproturon [3-(4-isopropylphenyl)-1,1-dimethylurea] effect. Chlorophyll fluorescence induction of algal cells treated with isoproturon showed inactivation of photosystem II (PSII) reaction centers and strong inhibition of PSII electron transport. A linear correlation was found (R2>or=0.861) between the change of cells density affected by isoproturon and the change of effective PSII quantum yield (PhiM'), photochemical quenching (qP) and relative photochemical quenching (qP(rel)) values. The cells density was also linearly dependent (R2=0.838) on the relative unquenched fluorescence parameter (UQF(rel)). Non-linear correlation was found (R2=0.937) only between cells density and the energy transfer efficiency from absorbed light to PSII reaction center (ABS/RC). The order of sensitivity determined by the EC-50% was: UQF(rel)>PhiM'>qP>qP(rel)>ABS/RC. Correlations between cells density and those photosynthetic-fluorescence parameters provide supporting evidence to use them as biomarkers of toxicity for environmental pollutants.

Effect of mercury on the polyphosphate level of alga Chlamydomonas reinhardtii.

In this study, the accumulation and toxicity effect of 1-7 µM of Hg was determined during 24-72 h on two strains of Chlamydomonas reinhardtii, CC-125 and CC-503 as a cell wall-deficient mutant, by monitoring the growth rate and the maximum quantum yield of Photosystem II. In addition, the level of extracytoplasmic polyphosphates (polyP related to the cell wall) was determined to understand the polyP physiological role in Hg-treated algal cells. The results showed that the polyP level was higher in the strain CC-125 compared to CC-503. When algal cells were exposed to 1 and 3 µM of Hg, the accumulation of Hg was correlated with the degradation of polyP for both strains. These results suggested that the degradation of polyP participated in the sequestration of Hg. In fact, this mechanism might explain at 72 h the recovery of the polyP level, the efficiency of maximum PSII quantum yield, the low inhibition of growth rate, and the low accumulated Hg in algal biomass. Under the effect of 5 and 7 µM of Hg, the degradation of polyP was complete and could not be recovered, which was caused by a high accumulation and toxicity of Hg already at 24 h. Our results demonstrated that the change of polyP level was correlated with the accumulation and effect of Hg on algal cells during 24-72 h, which can be used as a biomarker of Hg toxicity. Therefore, this study suggested that extracytoplasmic polyP in C. reinhardtii contributed to the cellular tolerance for Hg.

Effect of cadmium accumulation on green algae Chlamydomonas reinhardtii and acid-tolerant Chlamydomonas CPCC 121.

Cadmium is one of the most dangerous metals found in wastewater since exposure to low concentrations are highly toxic for cellular functions. In this study, the effect of cadmium accumulation on Chlamydomonas reinhardtii and acid-tolerant strain CPCC 121 was investigated during 48 h under 100-600 µM of Cd and two pH conditions (4 and 7). The toxicity of accumulated Cd was determined by the change of cellular and photosynthetic parameters. Obtained results showed that the maximum capacity of Cd accumulation in algal biomass was reached for both strains at 24 h of exposure to 600 µM of Cd. Under this condition, C. reinhardtii showed a higher uptake of Cd compared to the strain CPCC 121, inducing a stronger cellular toxic impact. Chlamydomonas CPCC 121 showed a tolerance for Cd due to the exclusion of Cd at the cell wall surface, which was higher at pH 4 than pH 7. TEM images and EDX spectrum of Cd distribution within the cell confirmed the role of the cell wall as a barrier for Cd uptake. Although Cd2+ concentration was the highest in the medium, CPCC 121 was the most tolerant at pH 4, but was not enough efficient to be considered for the phycoremediation of Cd. At neutral pH, the efficiency of C. reinhardtii for the removal of Cd was limited by its toxicity, which was dependent to the concentration of Cd in the medium and the time of exposure.

Toxicity of Nickel Oxide Nanoparticles on a Freshwater Green Algal Strain of Chlorella vulgaris.

A freshwater microalga strain of Chlorella vulgaris was used to investigate toxic effects induced by nickel oxide nanoparticles (NiO-NPs) in suspension. Algal cells were exposed during 96 h to 0-100 mg L-1 of NiO-NPs and analyzed by flow cytometry. Physicochemical characterization of nanoparticles in tested media showed a soluble fraction (free Ni2+) of only 6.42% for 100 mg L-1 of NiO-NPs, indicating the low solubility capacity of these NPs. Toxicity analysis showed cellular alterations which were related to NiO-NPs concentration, such as inhibition in cell division (relative cell size and granularity), deterioration of the photosynthetic apparatus (chlorophyll synthesis and photochemical reactions of photosynthesis), and oxidative stress (ROS production). The change in cellular viability demonstrated to be a very sensitive biomarker of NiO-NPs toxicity with EC50 of 13.7 mg L-1. Analysis by TEM and X-ray confirmed that NiO-NPs were able to cross biological membranes and to accumulate inside algal cells. Therefore, this study provides a characterization of both physicochemical and toxicological properties of NiO-NPs suspensions in tested media. The use of the freshwater strain of C. vulgaris demonstrated to be a sensitive bioindicator of NiO-NPs toxicity on the viability of green algae.

Changes in the room-temperature emission spectrum of chlorophyll during fast and slow phases of the Kautsky effect in intact leaves.

Changes in the room-temperature emission spectrum of chlorophyll (Chl) were analyzed using fast diode-array recordings during the Kautsky effect in mature and in greening barley leaves. In mature leaves, the comparison of F(O) (basal level of fluorescence yield at transient O) and F(M) (maximum level of fluorescence yield at transient M) spectra showed that the relative amplitude of total variable fluorescence was maximal for the 684 nm Photosystem II (PSII) band and minimal for the 725 nm Photosystem I band. During the increase from F(O) to F(M), a progressive redshift of the spectrum of variable fluorescence occurred. This shift reflected the different fluorescence rise kinetics of different layers of chloroplasts inside the leaf. This was verified by simulating the effect of screening on the emission spectrum of isolated chloroplasts and by experiments on greening leaves with low Chl content. In addition, experiments performed at different greening stages showed that the presence of uncoupled Chl at early-greening stages and light-harvesting complex II (LHCII) at later stages have detectable but minor effects on the shape of room-temperature emission spectra. When strong actinic light was applied to mature green leaves, the slow fluorescence yield, which declined from F(M) to F(T) (steady-state level of fluorescence yield at transient T), was accompanied by a slight redshift of the 684 nm PSII band because of nonphotochemical quenching of short-wavelength-emitting Chl ascribed to LHCII.