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The isotopic exchange reaction of iodine in fused NaI–NaIO3 and KI–KIO3 systems, which does not proceed until the mixture is melted, is found to be almost instantaneous in homogeneous melts. The equilibrium is attained within a period of less than 5 min at a temperature 5°C above the melting temperature of each composition for both systems. No noticeable exchange is observed even after heating the samples for 30 min at a temperature 20°C below the corresponding melting point. A single-step bimolecular association-dissociation mechanism is proposed for the exchange.

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Maize protein quality is deficit in essential amino acids, lysine and tryptophan. These constraints of o2 (opaque2) are corrected in genetically improved, hard endosperm QPM (Quality Protein Maize). An integrated strategy of phenotypic selection for endosperm modifiers and molecular marker-assisted foreground and background selection has been used in present study. The QPM donors were, CML 161, DMRQPM 58, CML 176 and CML 141 whereas, normal maize inbreds were CM 212, V338, V361, V336, V341, V351, CM 141 and V335. The inbreds were subjected to parental polymorphism survey between non-QPM and QPM using CIMMYT based three SSR markers, viz. phi057, umc1066 and phi112. Two markers, viz. phi057 and umc1066 exhibited co-dominant reactions, while phi112 was dominant in nature. Finally, two combinations V335 × CML 141 and V351 × CML 141 were considered for conversion program. Foreground selection was exercised using o2 specific marker umc1066 in BC1 and BC2 generations, while background as well as foreground selection was exercised in BC2F3 generation to recover the genome of recurrent parent up to extent of 80 to 100% with the help of SSR markers distributed across the whole maize genome. The tryptophan concentration in endosperm protein was significantly enhanced and the converted maize lines had almost twice the amount of lysine and tryptophan than normal maize inbreds.

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In the present investigation, expression of genes related to Na+ exclusion such as salt overly sensitive (TaSOS1) and Na+/H+ antiporter (TaNHX1) and proline accumulation such as pyrroline-5-carboxylate reductase (P5CR) and glutamate synthase (GOGAT) was studied in seedlings of Kharchia 65 (Kh 65, salt tolerant) and HD 2009 (sensitive) under salt stress (ECe, 12 dSm–1) and controlled conditions. As compared to HD 2009, Kh 65 showed significantly lower accumulation of Na+ (p < 0.01) and higher accumulation of proline (p < 0.05) in leaf blade under salt stress. The relative expression of TaSOS1 increased significantly (p < 0.001) in roots of Kh 65 (4.31-fold) while it decreased in HD 2009. There was significantly higher (p < 0.01) relative expression of TaNHX1 (27.57-fold) in leaf and 3.07-fold in roots of Kh 65 as compared to 3.65- and 0.87-fold increase in leaf and roots of HD 2009, respectively, under salt stress. There was significantly (p < 0.05) higher accumulation of proline as compared to HD 2009 in leaf tissues. There was significantly higher (p < 0.01) expression of P5CR (5.23-fold in leaf and 8.77-fold in the root) and glutamate synthase (6.0- fold in roots) in Kh 65 as compared to HD 2009. The study demonstrated that upregulation of genes for Na+ exclusion in root and compartmentation in leaf and increased proline concentration are associated with tolerance to salinity stress in wheat. The information will be useful for improving wheat genotypes for salt tolerance.

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Cereal Research Communications
Authors: R. Ponnuswamy, A. Rathore, A. Vemula, R.R. Das, A.K. Singh, D. Balakrishnan, H.S. Arremsetty, R.B. Vemuri, and T. Ram

The All India Coordinated Rice Improvement Project of ICAR-Indian Institute of Rice Research, Hyderabad organizes multi-location testing of elite lines and hybrids to test and identify new rice cultivars for the release of commercial cultivation in India. Data obtained from Initial Hybrid Rice Trials of three years were utilized to understand the genotype × environment interaction (GEI) patterns among the test locations of five different agro-ecological regions of India using GGE and AMMI biplot analysis. The combined analysis of variance and AMMI ANOVA for a yield of rice hybrids were highly significant for GEI. The GGE biplots first two PC explained 54.71%, 51.54% and 59.95% of total G + GEI variation during 2010, 2011 and 2012, respectively, whereas AMMI biplot PC1 and PC2 explained 46.62% in 2010, 36.07% in 2011 and 38.33% in 2012 of the total GEI variation. Crossover interactions, i.e. genotype rank changes across locations were observed. GGE biplot identified hybrids, viz. PAN1919, TNRH193, DRH005, VRH639, 26P29, Signet5051, KPH385, VRH667, NIPH101, SPH497, RH664 Plus and TNRH222 as stable rice hybrids. The discriminative locations identified in different test years were Coimbatore, Maruteru, VNR, Jammu, Raipur, Ludhiana, Karjat and Dabhoi. The AMMI1 biplot identified the adaptable rice hybrids viz., CNRH102, DRH005, NK6303, NK6320, DRRH78, NIPH101, Signet5050, BPH115, Bio452, NPSH2003, and DRRH83. The present study demonstrated that AMMI and GGE biplots analyses were successful in assessing genotype by environment interaction in hybrid rice trials and aided in the identification of stable and adaptable rice hybrids with higher mean and stable yields.

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