మా గ్రూప్ ప్రతి సంవత్సరం USA, యూరప్ & ఆసియా అంతటా 3000+ గ్లోబల్ కాన్ఫరెన్స్ ఈవెంట్లను నిర్వహిస్తుంది మరియు 1000 కంటే ఎక్కువ సైంటిఫిక్ సొసైటీల మద్దతుతో 700+ ఓపెన్ యాక్సెస్ జర్నల్లను ప్రచురిస్తుంది , ఇందులో 50000 మంది ప్రముఖ వ్యక్తులు, ప్రఖ్యాత శాస్త్రవేత్తలు ఎడిటోరియల్ బోర్డ్ సభ్యులుగా ఉన్నారు.
ఎక్కువ మంది పాఠకులు మరియు అనులేఖనాలను పొందే ఓపెన్ యాక్సెస్ జర్నల్స్
700 జర్నల్స్ మరియు 15,000,000 రీడర్లు ప్రతి జర్నల్ 25,000+ రీడర్లను పొందుతున్నారు
Dereje Shimelis, Kassahun Bantte and Tilaye Feyissa
In Ethiopia, sugarcane is being grown as an important cash and industrial crop among many crops and plays an important role for the development of the economy of the country. Improvement of this crop through conventional breeding takes 8 to 10 years and its propagation by cutting takes 6 to 7 years for commercial scale. During these periods of years the crop might starts to detiorarte genetically by biotic and abiotic factors. To solve the limitations, tissue culture (micropropagation) was born as best alternative. Once millions of shootlets multiplied in vitro by micropropagation, they should have roots to be transplanted to the field. Hence, this research was launched to optimize appropriate concentration of IBA (0, 1, 2 and 3) mgl-1 and NAA (0, 1, 2, 3, 4 and 5) mgl-1 combinations for root induction of C86-12 and C86-56 genotypes in completely randomized design with 4×6×2 factorial treatment combinations arrangements. The analysis of variance showed that the interaction effects of concentrations of IBA and NAA combinations and genotypes were highly significant (p=0.001) for mean number of roots per shoot and mean root length.1/2 MS medium supplemented with 2 mgl-1 IBA+1 mgl-1 NAA for C86-56 has gave best number of roots (14.88) but best root length (3.14 cm) was obtained on ½ MS+3 mgl-1 IBA+4 mgl-1 NAA. For C86-12 genotype 5 mgl-1 NAA alone has gave best number of roots (17.8) and root length (3.2 cm). Out 100 Plantlets taken for acclimatization from best media of root induction, 87% for C86-12 and 93% for C86-56 were survived. Thus these media combinations are the best media for induction of roots after multiplication stage of micropropagation for these genotypes.