Optimization study for refractance window drying process of Langra variety mango.

Refractance window (RW) drying of mango pulp has shown good quality retention compared to conventional drying methods. Different pulp thickness (2, 3 and 4 mm) and drying temperature (85, 90 and 95 °C) were optimized for RW drying of mango pulp for responses as drying time, ascorbic acid, total phenolics content (TPC) and hardness of mango leather. Face-centered central composite design was performed for optimization using Design-Expert software. RW drying of 2 mm thick mango pulp took the shortest drying time, however lower ascorbic acid and TPC were determined as compared to 3 mm and 4 mm thick pulp mango leather. Hardness of RW dried mango leather was determined to be in the chewable range as 3.62-5.33 N. The optimum solution generated for RW drying temperature and pulp thickness was 95 °C and 2.49 mm, respectively. The drying time was 22.5 min with high quality retention in terms of ascorbic acid, TPC and hardness as 62.33 mg/100 g DW, 7.72 mg GAE/g DW and 4.60 N respectively of dried product with desirability function obtained was 0.969. More nutrients were preserved in mango leather as well as microstructure of mango powder was observed as smooth and flaky with uniform thickness of powder particles with RW drying process when compared with tray and oven drying at 95 °C drying temperature and 2.50 mm mango pulp thickness.

Genesis of Influenza A(H5N8) Viruses.

Highly pathogenic avian influenza A(H5N8) clade 2.3.4.4 virus emerged in 2016 and spread to Russia, Europe, and Africa. Our analysis of viruses from domestic ducks at Tanguar haor, Bangladesh, showed genetic similarities with other viruses from wild birds in central Asia, suggesting their potential role in the genesis of A(H5N8).

Quantitative Analysis of Major Phytochemicals in Orthodox tea (Camellia sinensis), Oxidized under Compressed Air Environment.

This study describes major changes in phytochemical composition of orthodox tea (Camellia sinensis var. Assamica) oxidized under compressed air (CA). The experiments for oxidation were conducted under air pressure (101, 202, and 303 kPa) for 150 min. Relative change in the concentrations of caffeine, catechins, theaflavins (TF), and thearubigins (TR) were analyzed. Effect of CA pressure was found to be nonsignificant in regulating caffeine concentration during oxidation. But degradation in different catechins as well as formation of different TF was significantly affected by CA pressure. At high CA pressure, TF showed highest peak value. TR was found to have slower rate of formation during initial phase of oxidation than TF. Even though the rate of TR formation was significantly influenced by CA, a portion of catechins remained unoxidized at end of oxidation. Except caffeine, the percent change in rate of formation or degradation were more prominent at 202 kPa.