Effect of cryopreservation on pollen viability, fertility and morphology of different Psidium species.

Cryopreservation of pollen is a complementary conservation strategy and can be used for conserve the diversity in the genus Psidium. The present study aims to cryopreserve the pollen of Psidium species to overcome asynchronous flowering. The pollen of different Psidium species were germinated in vitro in an optimized medium of germination. In vitro/in vivo pollen viability assessment and SEM analysis were carried out to determine the changes after cryopreservation. The in vitro pollen viability was determined at monthly intervals starting from fresh pollen until six months of cryopreservation. The in vivo fertility tests were carried out by pollination using both fresh and cryopreserved pollen. The cryopreserved pollen showed in vitro germination ranging from 1.78% (in P. molle) to 81.67% (in "H 12-5") compared to fresh pollen (2.16% in P. molle to 86.08% in P. guineense). In vivo fertility was tested by controlled pollination using six-month-old cryopreserved pollen and it resulted in fruit setting ranged between 3.33% (P. cattleianum var. cattleianum) and 27.66% (P. chinensis) as compared to fresh pollen between 4.0% (P. cattleianum var. cattleianum) and 30.66% (P. chinensis). Seed set and germination was also recorded in all the crosses attempted using cryopreserved pollen. These in vitro and in vivo results indicated that cryopreservation is an effective technique for breeding and conserving the haploid gene pool in cryo genebank. Scanning Electron Microscopic studies of pollen revealed no significant variation in shape and size after cryopreservation when compared to fresh pollen.

Genotoxic effects of tobacco use in residents of hilly areas and foot hills of Western Ghats, Southern India.

Smoking and smokeless tobacco consumption is a significant risk factor that provokes genetic alterations. The present investigation was to evaluate the biomarkers of genotoxicity including micronucleus (MN), chromosome aberrations (CA) and DNA strand breaks among tobacco consumers and control individuals residing in hilly areas of Western Ghats, Tamilnadu, South India. This study included 268 tobacco consumers with equal number of controls. The tobacco consumers were divided into Group I (<10 years of tobacco consumption with an age range from 15 to 35 years) and group II (>10 years consumption above 35 years of age). Chromosome aberration (CA) and comet assay were performed using blood and micronucleus assay from exfoliated buccal epithelial cells obtained from tobacco consumers and controls. Elevated levels of CA were found in group II (Chromatid type: 2.39 ± 1.13 and chromosome type: 1.44 ± 1.24) exposed subjects, high micronucleus and DNA damage (TL:4.48 ± 1.24 and TM:3.40 ± 1.58) levels were significantly (p < 0.05) observed in both smoking and smokeless tobacco consumers when comparison with group I and controls. This study also observed a lack of awareness among the tobacco consumers about the harmful health effects of tobacco. Tobacco consumption contributes to the significant alteration in genetic materials. In addition, a high rate of spontaneous abortion was also seen in the studied population.