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Lanthanides are indispensable constituents of modern technologies and are often challenging to acquire from natural resources. The demand for REEs is so high that there is a clear need to develop efficient and eco-friendly recycling methods. In the present study, freeze-dried biomass of the polyextremophile Galdieria sulphuraria was employed to recover REEs from spent fluorescent lamps (FL) luminophores by pretreating the freeze-dried biomass with an acid solution to favour ion exchange and enhance the binding sites on the cell surface available for the metal ions. Lanthanides were extracted from the luminophores using sulfuric acid solutions according to standardised procedures, and the effect of biosorbent dosage (0.5-5 mg/ml) and biosorption time (5-60 min) were evaluated. The content of individual REEs in the luminophores and the resulting algal biomass were determined using inductively coupled plasma mass spectrometry (ICP-MS). The most abundant REE in the luminophores was yttrium (287.42 mg/g dm, 91.60% of all REEs), followed by europium (20.98 mg/g, 6.69%); cerium, gadolinium, terbium and lanthanum was in trace. The best biosorption performances were achieved after 5 min and at the lowest biosorbent dosage (0.5 mg/mL). The highest total metal amount corresponded to 41.61 mg/g dried mass, and yttrium was the most adsorbed metal (34.59 mg/g dm, 82.88%), followed by cerium (4.01 mg/g); all other metals were less than 2 mg/g. The rapidity of the biosorption process and the low biosorbent dosage required confirmed this microalga as a promising material for creating an eco-sustainable protocol for recycling REEs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

The toxic effects of Triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether) on morphology and sexual and asexual reproduction of C. ehrenbergii were examined. In addition, the genotoxic effects of Triclosan were evaluated on the same alga using the microgel electrophoresis test, also-called Comet assay. Increasing Triclosan concentrations in the range 0.125-5 mg L(-1) did not affect size and shape of the cells but had relevant effects on both chloroplast morphology and dimension. Triclosan inhibited the vegetative growth of C. ehrenbergii at 0.5 mg L(-1). The effects on sexual reproduction indicate that the number of C. ehrenbergii zygospores was significantly reduced by the application of 0.937 mg L(-1). The Comet assay showed that Triclosan treatments led to a dose-dependent DNA damage of C. ehrenbergii; 0.25 mg L(-1)caused significant genotoxic effects and higher concentrations irreversibly altered the DNA strands. These results suggest that C. ehrenbergii could represent a useful organism to evaluate the whole toxicity of pharmaceuticals and personal care products (PPCPs), giving valuable information for a risk assessment.