Genotype, age of tree, nature of explant and size (length and diameter), season of explant collection, explant position on medium, plant growth regulators and certain additives (ascorbic and citric acids, adenine sulphate, L-arginine, glutamine and ammonium citrate), incubation conditions, and subculturing period greatly influenced the in vitro clonal propagation of P. cineraria. The maximum number of lo-12 shoots were induced from the nodal shoot segment from pruned thorny adult trees on Murashige and Skoog's (MS) medium containing 0.1 mgl-' indole-3-acetic acid (IAA) + 2.5 mgl-' benzylaminopurine (BAP) + additives. Higher temperature (31 f 2 "C) and mixed (fluorescent and incandescent) light of 50 pmol me2 s-' photon flux density for 12 h per day photoperiod favoured shoot induction and subsequent growth. Explants from thornless trees produced 6-8 shoots per explant on MS medium containing 0.1 mgll' IAA + 5.0 mgll' BAP + additives. Nodal shoot segments obtained from root and stump sprouts produced multiple shoots. Root segments differentiated into multiple shoots on MS medium containing 0.5 mgll' indolebutyric acid (IBA) + 2.5mgll' BAP.Differentiated shoots multiplied best on MS medium containing 0.1 mgll' naphthalene acetic acid (NAA) + 1 .O mgl-' BAP + additives. To yield multiple shoots the original explant was transferred 6 times on fresh medium after harvesting the differentiated shoots. Shoots were rooted by pulsing with 100 mgll' IBA for 4 h and then culturing on hormone-free half strength MS medium. Initial dark incubation for 5 days at high temperature (33 f 2OC) was found essential for root induction from shoots which was 63% within two weeks. The rooted plantlets contained a consistent number of chromosomes (2 n = 28). It is suggested that the protocol developed could be useful for cloning of mature and tested trees of P. cineraria.
Sweet sorghum [Sorghum bicolor (L.) Moench] has potential as a bioenergy crop for producing food, fiber, and fermentable sugar. Unlike dryland grain sorghum, little information is available on the influence of staggered planting and genotypes, especially in semiarid tropical environments. The objectives of the present study were (i) to quantify the effects of planting time and genotype on stalk and biomass yields, juice sugar quality, and (ii) to identify the most productive genotypes and planting windows for sustainable feedstock supply. Four commercial sweet sorghum genotypes (SSV84, SSV74, CSV19SS, and CSH22SS) were planted on five planting dates (1 June, 16 June, 1 July, 16 July, and 1 August) during the rainy (June–October) season of 2008 and 2009 in Hyderabad (17°27´ N, 78°28´ E), India. Planting in early and mid‐June produced significantly (P ≤ 0.05) higher fresh stalk yield and grain yield than later planting dates. Commercial hybrid CSH22SS produced significantly more stalk, grain, sugar, and ethanol yield over genotypes SSV84 or SSV74. Based on the stalk yield, juice sugar quality, sugar, and ethanol yields, the optimum planting dates for sweet sorghum in semiarid tropical climate is early June to early July. Planting sweet sorghum during this time allows more feedstock to be harvested and hence extends the period for sugar mill operation by about 1 mo, that is, from the first to the last week of October.
Interspecific hybridization is an important tool to elucidate intergenomic relationships, transfer characters across species and develop synthetic amphidiploids, and it has been widely applied for improving brassicas. The objective of the present study was to create genetic variability in Brassica through interspecific hybridization. Crosses between Brassica juncea (AABB, 2n ¼ 36), and Brassica rapa (AA, 2n ¼ 20) vars toria, yellow sarson, and brown sarson were attempted, and the hybrid derivatives were advanced to the F 4 generation. Hybrids were obtained from the crosses B. juncea · toria and B. juncea · yellow sarson. The F 1 plants were vigorous and intermediate to the parents in many morphological traits. The meiotic study of AAB hybrids showed 10 II + 8 I in the majority (71.8%) of cells analysed. A maximum of 12 and a minimum of seven bivalents were also observed in a few cells. The occurrence of multivalent associations (trivalents to pentavalents) at diakinesis/metaphase I and a bridgefragment configuration at anaphase I were attributed to homoeology between A and B genomes. A high percentage of plants resembling B. juncea was observed in the F 2 generation. Transgressive segregation in both directions was found for plant height, primary branches, main raceme length, siliquae on main raceme, siliqua intensity, seeds per siliqua and seed yield. There were significant differences for the 14 characters in the F 4 derivatives. Moderate to high estimates of phenotypic and genotypic coefficients of variation, broad-sense heritability, and expected genetic advance were found for seed yield, 1000-seed weight, siliquae per plant, seeds per siliqua and days to flowering. Intergenomic recombination, reflected as wide variation in the hybrid progenies, permitted the selection of some useful derivatives.
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