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Physiology and Molecular Biology of Stress ... - KHAM PHA MOI

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Nutrient <strong>Stress</strong><br />

207<br />

Table 16.<br />

Relationship between chloride content in leaves <strong>and</strong><br />

growth disorders in coconut plants*<br />

KCl application Leaf content Growth disorders (%)<br />

(Kg/plant)<br />

(% dry wt.)<br />

K Cl Frond fracture Stem cracking<br />

0 1.61 0.07 11.6 27.0<br />

2.25 1.64 0.41 1.7 8.1<br />

4.50 1.66 0.51 1.2 4.5<br />

*Adapted from Von Uexkull (1985).<br />

Chloride toxicity is a worldwide phenomenon <strong>and</strong> is an important factor limiting<br />

plant growth. The general symptoms are burning <strong>of</strong> leaf tips or margins, bronzing,<br />

premature yellowing <strong>and</strong> abscission <strong>of</strong> leaves. In some cases growth is reduced without<br />

any visual symptoms.<br />

15. NICKEL<br />

Nickel is a recently discovered micronutrient that can form chelate compound <strong>and</strong> can<br />

replace other heavy metals from physiologically important centres <strong>of</strong> metabolism. Most<br />

<strong>of</strong> the soils contain small quantities <strong>of</strong> nickel (< 100 ppm). Nickel is closely related to<br />

iron <strong>and</strong> cobalt in chemical <strong>and</strong> physiological properties. Although nickel may exist in<br />

the oxidation state <strong>of</strong> Ni(I) <strong>and</strong> Ni(II) but the most preferred oxidation state in biological<br />

system is Ni(II) (Cammack et al., 1988).<br />

The function <strong>of</strong> nickel in higher plants was first time shown by Dixon et al.,<br />

(1975) in connection with the urease activity. Eskew et al., (1984) reported that leguminous<br />

plants require nickel irrespective <strong>of</strong> the form <strong>of</strong> nitrogen source. Later, the essentiality<br />

<strong>of</strong> nickel for non-legumes was established (Brown et al., 1987). By these findings<br />

nickel is regarded as an essential element. Nickel is a component <strong>of</strong> urease, microbial<br />

dehydrogenases, hydrogenases <strong>and</strong> methyl reductase. It plays a significant role in urea<br />

<strong>and</strong> ureide metabolism, iron absorption, nitrogen fixation <strong>and</strong> seed development.<br />

Nickel-deficient cowpea plants accumulated large amount <strong>of</strong> urea in tip <strong>of</strong> the<br />

leaf blade. Ureide levels were not affected by nickel supply (Walker et al., 1985). Brown<br />

et al., (1990) found that in barley the critical deficiency level <strong>of</strong> Ni is about 0.1 µg/g dry<br />

weight <strong>and</strong> associated with the accumulation <strong>of</strong> nitrate <strong>and</strong> amino acids. Nickel deficient<br />

plants show interveinal chlorosis <strong>and</strong> necrosis in leaves. Normally the nickel<br />

content <strong>of</strong> many plants is in the range <strong>of</strong> 1-10 µg/g dry matter. In some plants like lupin,<br />

nickel is preferentially translocated to seeds (Table 17).

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