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Dr. Y. S. Parmar University of Horticulture & Forestry, Solan

Dr. Yashwant Singh Parmar University of Horticulture and Forestry, Solan, was established on 1st December, 1985 with the objective to promote education, research and extension education in the fields of Horticulture, Forestry and allied disciplines. Late Dr. Yashwant Singh Parmar, the first Chief Minister and the architect of Himachal Pradesh perceived the importance of Horticulture and Forestry to develop and improve the State economy which led to the establishment of this University. Its history lies in erstwhile Himachal Agricultural College, Solan, established in 1962 and affiliated to the Panjab University. It became one of the campuses of Agriculture Complex of Himachal Pradesh University on its formation in 1970. Consequent upon the establishment of Himachal Pradesh Krishi Vishvavidyalaya in 1978, this campus became its Horticulture Complex and finally in 1985, assumed the status of a State University, being the only University in the country engaged exclusively in teaching, research and extension in Horticulture and Forestry. The University is located at Nauni in Solan District of Himachal Pradesh, 13 km from Solan on Solan-Rajgarh Road, at an elevation of 1300 metres above mean sea level. Solan town is situated on national highway (NH-22) and is well connected by train and bus services. The University has four constituent colleges, out of which, two are located at the main campus Nauni, one for horticulture and the other for forestry, having 9 and 7 departments, respectively. The third College i.e., College of Horticulture & Forestry is located at Neri in Hamirpur District on Nadaun-Hamirpur state highway, about 6 Km from Hamirpur town and is well connected with bus service. The college offers three Undergraduate Degree Programmes i.e. BSc (Hons.) Horticulture, BSc (Hons.) Forestry and B. Tech. Biotechnology and MSc degree programme in a few subjects. The fourth college i.e. College of Horticulture and Forestry, Thunag (Mandi) is located at Thunag District Mandi. This college offer BSc (Hons.) Horticulture and BSc (Hons.) Forestry degree programme. In addition, there are five Regional Research Stations, 12 Satellite Stations and five Krishi Vigyan Kendras (KVKs) situated in different zones of the State.

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20193
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Subject: Biotechnology × End date: 2019 × Start date: 2019 × Thesis Type: M.Sc ×
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    ThesisItemOpen Access
    STUDIES ON IN VITRO REGENERATION OF ENDANGERED MEDICINAL PLANT NAG CHHATRI (TRILLIUM GOVANIANUM WALL. EX D. DON)
    (UHF,NAUNI, 2019-12) KUMAR, VINAY; SHARMA, RAJNISH
    ABSTRACT The present investigations were aimed at “Studies on in vitro regeneration of endangered medicinal plant nag chhatri (Trillium govanianum Wall. ex D. Don)”. Plant material was procured from the natural habitat and different parts viz., seeds, roots, rhizome discs, rhizome buds, stems and leaves were used as explants for in vitro regeneration. Highest per cent survival 86.67%, 84.45%, 83.33% and 93.33% was observed in seed, root, rhizome disc and rhizome bud explants, respectively when treated with 0.2% carbendazim for 5 mins along with 0.1% HgCl2 for 3 mins while phytotoxic effect of different sterilants was observed on leaf and stem explants. Out of different explants used, rhizome buds showed 96.67% shoot regeneration on MS medium supplemented with 0.5 mg/l BAP, 0.5 mg/l kinetin, 0.5 mg/l GA3 with average shoot length of 4.33 cm after 4 weeks of culturing. Modified MS medium containing ammonium sulphate, 7.00 mM CaCl2and 0.2 mM Fe-EDDHA was used for shoot regeneration to overcome the problem of leaf chlorosis that was observed after one week from shoot proliferation. Substantial increase in the production of lateral buds and mini rhizomes was found on MS medium enriched with 6% sucrose, 0.5 mg/l BAP, 0.5 mg/l kinetin, 0.5 mg/l GA3 and 100 mg/l casein hydrolysate with 93.33% bud production. Higher concentration of sucrose, growth regulators (BAP & TDZ) and additives (casein hydrolysate & L-glutamine) showed significant effect on mini rhizomes production from in vitro derived lateral buds. Number of experiments were carried out for inducing in vitro rooting in regenerated shoots and mini rhizomes using different auxins on half strength and full strength media, respectively, but rooting couldn’t be achieved because of the browning of established shoots and mini rhizomes. Therefore, it was inferred that the present study would be helpful towards various in vitro conservation practices of this valuable medicinal herb in near future. Keywords: In vitro regeneration,Trillium govanianum, Rhizome, Lateral bud, Mini rhizome, Medicinal herb
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    ThesisItemOpen Access
    STUDIES ON COST EFFECTIVE IN VITRO PROPAGATION OF PLUM (Prunus salicina L.) CV. SANTA ROSA
    (UHF,NAUNI, 2019-09) HARISHCHANDRA, SHERKAR SANDIP; THAKUR, MANISHA
    ABSTRACT Plum (Prunus salicina L.) is one of the important temperate fruit crops of the world. It belongs to family Rosaceae and sub family Prunoideae. In the present investigation, a technique for cost effective in vitro propagation of plum cv. Santa Rosa has been developed. It was observed that table sugar (40 g/l) and isabgol (10 g/l) can be used as low cost alternatives for sucrose and agar, respectively. Out of different combinations tried, 10 g/l isabgol and 30 g/l sucrose showed maximum shoot multiplication rate of 1:6 with 2.36 cm average shoot length, which was better as compared to control having shoot multiplication rate of 1:4 with average shoot length of 2.22 cm. On the other hand when isabgol was combined with 40 g/l table sugar showed shoot multiplication rate of 1:4 with average shoot length of 2.12 cm was obtained which was similar to control. With the increase in number of passages shoot multiplication rate increased in all the above mentioned medium. Best rooting (60%) was observed on 1/3rd strength liquid control medium with 15 roots per shoot, followed by 1/3rdLCR2with 11.33 roots per shoot. Dark treatment of 48 hours enhanced rooting in both the above mentioned rooting medium. For hardening different potting mixtures were tested but maximum per cent survival 75% was observed on cocopeat. For increasing the hardening percentage biohardening was tested by using Jeevamrit and PGPR (Bacillus licheniformis). It was observed that drenching 20 ml of Jeevamrit (3%) resulted in 60% plantlet survival whereas, 50% survival could be achieved when 5 ml of PGPR was poured around each plantlet. Cost analysis of various medium used showed that there was a significant difference between cost of low cost medium and control. Per plantlet cost in control medium was calculated to be Rs. 1.33 whereas, in low cost medium containing isabgol + sucrose (LCM2) and isabgol + table sugar (LCM5) during multiplication and 1/3rd LCR2 during rooting it was calculated to be Rs 0.40 and 0.22, respectively, showing 59.92% and 77.55% cost reduction. Therefore table sugar and isabgol can be successfully used as an inexpensive alternative to sucrose and agar for commercial multiplication of plum cv. Santa Rosa at economical rates.
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    ThesisItemOpen Access
    IN VITRO PROPAGATION OF A BIOTYPE OF CRAB APPLE [MALUS BACCATA (LINN.) BORKH. (SHILLONG)]
    (UHF,NAUNI, 2019-02) ANJALI; MODGIL, MANJU
    ABSTRACT The present studies were made to establish and proliferate shoots using axillary buds as explants during in vitro propagation of crab apple biotype Shillong. Shoot cuttings were collected in different months of the year from trees growing at the Dhanda farm of the Regional Research Station of IARI, Shimla (H.P.). Surface sterilization with 1.0% NaOCl for 20 mins was found more effective as compared to higher concentrations. Rinsing of phenols in liquid MS medium containing PVP (1g/l) and AC (1g/l) was found essential for explants survival and successful establishment of buds. The explants of 1-1.5cm size resulted in medium phenol intensity and maximum bud break (6.67%). MS medium supplemented with 2mg/l BA, 0.5 mg/l GA3 and 0.1 mg/l IBA resulted in maximum bud break of 40.13% and bud survival of 19.66% after 1st subculture when buds were collected in April month. However, some of the proliferated shoots did not grow further which may be due to the internal contamination of bacteria. These shoots turned brown and became necrotic. Shoots did not induce multiple/axillary shoots in four combinations of growth regulators. Addition of appropriate antibiotics in culture medium to inhibit the bacterial growth or meristem culture may be used in fu