Ecological disturbances and abundance of anthropogenic pollutants in the aquatic ecosystem: Critical review of impact assessment on the aquatic animals.

Anthropogenic toxins are discharged into the environment and distributed through a variety of environmental matrices. Trace contaminant detection and analysis has advanced dramatically in recent decades, necessitating further specialized technique development. These pollutants can be mobile and persistent in small amounts in the environment, and ecological receptors will interact with it. Despite the fact that few researches have been undertaken on invertebrate exposure, accumulation, and biological implications, it is apparent that a wide range of pollutants can accumulate in the tissues of aquatic insects, earthworms, amphipod crustaceans, and mollusks. Due to long-term stability during long-distance transit, a number of chemical and microbiological agents that were not previously deemed pollutants have been found in various environmental compartments. The uptake of such pollutants by the aquatic organism is done through the process of bioaccumulation when dangerous compounds accumulate in living beings while biomagnification is the process of a pollutant becoming more hazardous as it moves up the trophic chain. Organic and metal pollution harms animals of every species studied so far, from bacteria to phyla in between. The environmental protection agency says these poisons harm humans as well as a variety of aquatic organisms when the water quality is sacrificed in typical wastewater treatment systems. Contrary to popular belief, treated effluents discharged into aquatic bodies contain considerable levels of Anthropogenic contaminants. This evolution necessitates a more robust and recent advancement in the field of remediation and their techniques to completely discharge the various organic and inorganic contaminants.

Assessment, characterization, and quantification of microplastics from river sediments.

Microplastic (MP), as a pollutant, is currently posing a biological hazard to the aquatic environment. The study aims to isolate, quantify, and characterize the MP pollutants in sediment samples from 14 study sites at Kaveri River, Killa Chinthamani, Tiruchirappalli, South India. With Sediment-MP Isolation (SMI) unit, density separation was done with a hydrogen peroxide solution. Four forms of MPs namely, fragments, films, foams, and fibers with orange, white, green, and saffron red were observed. The plenitude and distribution of four forms of MPs and natural substrates were geometrically independent, with large amounts of microfragments within the research region accounting for 79.72% variation by Principal Component Analysis. FT-IR analyses of MPs showed the presence of polyamide, polyethylene, polyethylene glycol, polyethylene terephthalate, polypropylene, and polystyrene. Additionally, the scanning electron microscopic analysis revealed that the MPs have differential surface morphology with rough surfaces, porous structures, fissures, and severe damage. Most MPs comprised Si, Mg, Cu, and Al, according to energy dispersive X-ray analyses. The combined SMI, instrumental analyses and evaluation (heat map) of MPs in river sediments help assess contamination levels and types of MPs. The findings might provide an insight into the status of MPs in Kavery River sediments that could help in formulating regulations for MPs reduction and contamination in rivers eventually to protect the environment.

Aqueous two-phase partitioning and characterization of xylanase produced by Streptomyces geysiriensis from low cost lignocellulosic substrates.

Microbial production of xylanase is gaining the commercial importance, due to its wide range of applications from paper and pulp to food and feed industries. Streptomyces geysiriensis was used for the production of extracellular xylanase from lignocellulosic substrates such as rice bran and saw dust, under solid-state fermentation. The influence of pH, temperature and incubation period for the maximum production of xylanase was investigated with 1:2 (w/v) of substrate to moisture ratio at 100 rpm shaking conditions. The maximum production was recorded after 5 days of fermentation with pH 8.0 at 40 °C. The scale-up was done based on the results of optimized parameters using 3 L Applikon autoclavable bioreactor with maximum yield of 186 U/ml after 4 days of fermentation. Extracellular xylanase was separated by partitioning in aqueous two-phase system consisting of 20% polyethylene glycol 6000 and 12% K2HPO4 with maximum yield of 93.97%. The investigation of the effect of pH and temperature and its incubation time showed that xylanase was retained its activity in a pH range of 6.5-8.5, with thermal stability from 20 °C to 60 °C up to 180 min. The presence of metal ions was found to inhibit the activity of xylanase especially Cu2+ and Zn2+. Xylanase was stable both at 4 °C and room temperature (35 °C) for 30 and 9 days respectively. The kinetic parameters Km (0.48 mg/ml) and Vmax (8.33 U/mg) were determined using birchwood xylan as substrate.