Arsenic (As) contamination of the environment has emerged as a concerning issue recently for which phytoremediation has been suggested as a viable solution. Hydrilla verticillata (L.f.) Royle is a widely distributed rapidly growing aquatic weed possessing significant potential to accumulate As and is thus a potential candidate for the purpose of As phytoremediation. In the present study, an investigation of thiol metabolism was conducted in H. verticillata, which revealed differential effects upon exposure to arsenite [As(III)] and arsenate [As(V)]. The accumulation of arsenic was found to be higher upon exposure to As(III) than to As(V). Besides, As(III) was found to induce the activities of enzymes, such as cysteine synthase and γ-glutamylcysteine synthetase and the amounts of cysteine and glutathione (GSH) to higher levels than that observed with As(V). The activity of glutathione-S-transferase was, however, stimulated to a higher level upon exposure to As(V) than As(III). The activity of arsenate reductase was found to increase upon As(V) exposure at all concentrations and durations. In addition, a significant stimulation in the activity of phytochelatin synthase was noticed in vitro with an increase in As/GSH concentration and time of incubation. Arsenic detoxification in H. verticillata thus appeared to involve an induction of thiol synthesis and consumption in a coordinated manner, though differentially upon exposure to As(III) and As(V). The information gained through this study would help in better designing of the pilot experiment at the field level depending on the chemical composition of the contaminated water.

The higher areal productivity and lipid content of microalgae and aquatic weed makes them the best alternative feedstocks for biodiesel production. Hence, an efficient and economic method of extracting lipid or oil from aquatic weed, Salvinia molesta is an important step towards biodiesel production. Since Salvinia molesta is an unexplored feedstock, its total lipid content was first measured as 16 % using Bligh and Dyer’s method which was quite sufficient for further investigation. For extracting more amount of lipid from Salvinia molesta, methanol: chloroform in the ratio 2:1 v/v was identified as the most suitable solvent system using Soxhlet apparatus. Based on the literature and the preliminary experimentations, parameters such as solvent to biomass ratio, temperature, and time were identified as significant for lipid extraction. These parameters were then optimized using response surface methodology with central composite design, where experiments were performed using twenty combinations of these extraction parameters with Minitab-17 software. A lipid yield of 92.4 % from Salvinia molesta was obtained with Soxhlet apparatus using methanol and chloroform (2:1 v/v) as solvent system, at the optimized conditions of temperature (85 °C), solvent to biomass ratio (20:1), and time (137 min), whereas a predicted lipid yield of 93.5 % with regression model. Fatty acid methyl ester (FAME) analysis of S. molesta lipid using gas chromatograph mass spectroscopy (GCMS) with flame ionization detector showed that fatty acids such as C16:0, C16:1, C18:1, and C18:2 contributed more than 9 % weight of total fatty acids. FAME consisted of 56.32, 28.08, and 15.59 % weight of monounsaturated, saturated, and polyunsaturated fatty acids, respectively. Higher cetane number and superior oxidation stability of S. molesta FAME could be attributed to its higher monounsaturated content and lower polyunsaturated content as compared to biodiesels produced from C. vulgaris, Sunflower, and Jatropha.

Aquatic weed Myriophyllum spicatum L. is one of the most invasive water plants known. In many countries, it is usually harvested and landfilled, where aerobic and anaerobic decomposition takes place. In this research, the kinetic, equilibrium, and desorption studies of biosorption of Pb(II), Cu(II), Cd(II), Ni(II), and Zn(II) ions onto compost of M. spicatum were investigated in batch experiments. Biosorbent was characterized by scaning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). SEM analysis showed that ion exchange between divalent cations Ca(II) and selected metals takes place. The results of FTIR exposed that carbonyl, carboxyl, hydroxyl, and phenyl groups are main binding sites for those heavy metal ions. The rate of adsorption of the five heavy metals was fast, which achieved equilibrium in 40 min, and followed the pseudo-second-order model well. Langmuir, Freundlich, and Sips equilibrium adsorption models were studied, and Sips isotherm gave the best fit for experimental data. Desorption by 0.1 M HNO₃did not fully recover the metals sorbed onto the compost, indicating that reusing this material as biosorbent is not possible. Furthermore, the use of spent biosorbent as a soil fertilizer is proposed.