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Results and Discussion

Chemical analysis of plant samples of all the genotypes for mineral uptake efticiency and distribution at various ontogenetic stages of Triticum aestivum L. is depicted in Tables 2 to 4. Mutant-37 of Indus-66 displayed significantly (P>=.01) higher uptake of N than all the other genotypes at all sampling dates in both sets of experiments. The N uptake of M-38 of C-591 was significantly higher than its mother cultivar at all sampling dates. In most of the cases Nayab mutants have higher N uptake than their parent and Mexi- Pak. However, Nayab mutant-27 was characterized by low grain N and high straw N content (LARIK et al 1984b). This observation indicate that this particular mutant is unable to transfer the absorbed N from shoot to the grain. This physiological function is undoubtedly gene controlled and differences are therefore inherited and gene probably determine not the character of complex, but the total uptake of an element in any specific environment (SINGH & LAMB 1970). Similarly, most of the Indus mutants were higher in N uptake than their parents and Mexi -Pak (Tables 2 to 4). M-27 was consistently higher than parent and Mexi-Pak at all sampling dates. The differential uptake of this mutant suggest that it has a greater uptake efficiency as a result of either a stronger root system or greater suction pressure. This probably accounts for the greater nitrogen absorption of this mutant. On the contrary, low N content of M-13 of Indus-66 in field experiment and M-28 and 38 of C-591 in pot experiment at maturity indicate the rapid translocation of N to aerial parts. Similar varietal differences in N uptake and utilization have been reported by a number of workers (MCNEAL et al 1966 ; GASSER & IORDANOV 1967 ; BRAUN & FISCHBECK 1976).

Mutants with superior P uptake and accumulation were also identified in the present work (Tables 2 to 4). All mutants of Indus-66 had significantly (P>=.01) higher uptake and accumulation of P at all sampling dates than their parent and commercial variety Mexi-Pak. M-38 of C-591 displayed higher P uptake than its mother cultivar at all sampling dates except at second harvest and at maturity in pot condition. Therefore, these mutants can be classified as P-efiicient mutants as suggested by BROWN (1966), because of their high P uptake capabilities from the growing media. On the other hand, Nayab mutants showed differential response to P uptake. These studies clearly suggest genetic control of P accumulation differences (BARBER et al 1967 ; LYNESS 1936 ; SAGGAR et al 1974).

The behaviour of the genotypes for K uptake and accumulation is presented in Tables 2 to 4. Generally the mutant genotypes have displayed improvement in K uptake at different sampling dates under both sets of conditions. Mutant-38 consistently exhibited higher K uptake compared to its mother cultivar at various ontogenetic stages under both conditions. Nayab mutants had significantly higher K uptake than their parent. The behaviour of M-37 of Indus-66 was not consistent. However, this mutant showed significant deviations than the parent and Mexi-Pak in K uptake potentialities. These results further points to the genotypic differences in K uptake and accumulation as well (CACCO et al 1976 ; GORSLINE et al 1961 ; KLEESE et al 1968, WALKER & SCHILLINGER 1975). These authors suggested that there are wide varietal differences in such genetically determined properties as ion transport and utilization.



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