04.06.2016 Views

Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

Vergara - 1976 - Physiological and morphological adaptability of ri

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

(TROWTH AND NTJTRIENT UPTAKE OF RITE ROOTS 269<br />

EFFECT OF LIGHT INTENSITY AND TEMPERATURE ON GROWTH<br />

0F ROOTS OF LOWLAND RICE<br />

The growth <strong>of</strong> a <strong>ri</strong>ce plant advances in a chain <strong>of</strong> shoot units <strong>and</strong> roots emerge<br />

as a unit. This shoots elongation syrnchronized with the upper third node leaf<br />

blade <strong>and</strong> may complicate the study’ <strong>of</strong> <strong>ri</strong>ce root growth as affected by climatic<br />

factors such as light intensity" <strong>and</strong> temperature. The regula<strong>ri</strong>ty <strong>and</strong> i11terdependence<br />

in emergence <strong>and</strong> elongation <strong>of</strong> roots <strong>and</strong> leaves should be closely<br />

related to the transloeation <strong>and</strong> circulation <strong>of</strong> metabolites in <strong>ri</strong>ce plants. 111<br />

studying the translocation <strong>of</strong> photosynthetic products from leaves to roots <strong>of</strong><br />

<strong>ri</strong>ce at yjoung panicle initiation, a stage <strong>of</strong> the most vigorous emergence <strong>and</strong><br />

elongation <strong>of</strong> roots, Yoshida (1968) ShOWCd that the rate <strong>of</strong> sucrose translocation<br />

per day amounted to 5 to 10% <strong>of</strong> the dry weight <strong>of</strong> roots (Table 1). But<br />

more than 90% <strong>of</strong> the nitrogen absorbed by roots was supplied to the ae<strong>ri</strong>al<br />

parts at that growth stage (Yoshida <strong>and</strong> Takahashi. 1958; Inada, 1967).<br />

The interrelation between ae<strong>ri</strong>al <strong>and</strong> underground organs in the mutual<br />

lranslocation <strong>of</strong> metabolites would result in the change in ae<strong>ri</strong>al parts, affecting<br />

the roots in a relatively short time, <strong>and</strong> vice versa. A conspicuous example <strong>of</strong><br />

such interrelation is the effect <strong>of</strong> light intensity’ on the growth <strong>of</strong> roots. Decrease<br />

in light intensity’ by shading almost completely’ interrupted dry matter increase<br />

in both ae<strong>ri</strong>al <strong>and</strong> underground parts (Oshima <strong>and</strong> Murayama. 1960). Moreover,<br />

shading more markedly affected roots than shoots, decreasing the R/T<br />

ratio (Yazaiva, 1955, unpublished), <strong>and</strong> disturbing the synchronized emergence<br />

<strong>of</strong> roots <strong>and</strong> leaves; that is, root emergence was started midway in the formation<br />

<strong>of</strong>the related leaf. which remained unaltered even under 50% reduction in light<br />

intensity (Komatsu, 1961). Since light does not directly‘ influence <strong>ri</strong>ce roots that<br />

grow in paddy soil, the foregoing facts are att<strong>ri</strong>buted with certainty to the decrease<br />

in photosynthate supply’ to the roots which was more rapid than the<br />

reduction in photosynthesis in green organs <strong>of</strong> <strong>ri</strong>ce. Actually, Yazawa (1960,<br />

unpublished) observed that when light intensity was reduced by 50% through<br />

shading. the total sugar content in roots after 12.5 hours fell to 50% <strong>of</strong> the eontrol,<br />

whereas that in leaves fell 79%. indicating that more acute shortage <strong>of</strong><br />

sugar took place in roots (Table 2).<br />

The effect <strong>of</strong> temperature on root growth has been studied by many workers,<br />

but the results are to some extent contradictory’. Nagai <strong>and</strong> Matsushita (1963)<br />

Table 1. Rate oil‘ sucrose translocation from leaves to roots in lowl<strong>and</strong> <strong>ri</strong>ce at young<br />

panlcle initiation tYoshtda, 196B).<br />

Specific activity <strong>of</strong><br />

Sucrose transloeation<br />

Nitrogen source in sucrose translocated (mgtg dw <strong>of</strong> root)<br />

culture solution (cprnfmg C) per hour per day<br />

No nitrogen 4,326 5.08 121.8<br />

Ammonium-N 18,368 1.91 455<br />

Nitrate-N 18,359 1.92 46 D

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!