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C - Lublin

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of the fresh sample, segregated all the samples into four classes of secondary<br />

transformation state. The first class of W 1 value ranging from 0,36 to 0,45<br />

comprises moorsh formations of initial state of secondary transformations, the fifth<br />

class of W 1 >0,90 holds for totally degraded moorshes (Gawlik J., 1992; Gawlik J.<br />

and Harkot W. 2000).<br />

Homoionic hydrogen forms of fresh moorsh materials containing exactly 0,4 g<br />

of dry organic matter were treated by NaOH solutions at pH = 5, 6, 7, and 8 at<br />

1:100 w/w solid to liquid ratio. Concentrations of the DOM in the extracts (0.45<br />

µm filtrates) were determined spectrophotometrically at 470 nm using Jasco V-500<br />

apparatus (MacCarthy P. and Rice J.A., 1985). A calibration curve was based on<br />

sodium humate solutions (Aldrich H1, 675-2).<br />

RESULTS AND DISCUSSION<br />

The amounts of DOM which was released in the process of alkalization are<br />

shown in Figure 1.<br />

2.5<br />

DOM(pH)=0.01exp(b 1 *pH)<br />

c [mg/ml]<br />

2<br />

1.5<br />

1<br />

0.5<br />

0<br />

1W 1 =0,74<br />

W 1 =0,48<br />

4 5 6 7 8 9<br />

pH<br />

Fig. 1. Concentration of organic matter released at various pH’s.<br />

The dissolution of soil organic matter was significantly affected by pH. At low,<br />

initial pH values, the dissolved organic matter concentration was small. Changes<br />

in pH affect the electrostatic charge that induces repulsion-attraction of negatively<br />

charged surfaces of humic acids to other soil components. Generally the increase in<br />

pH resulted in the increase in dissolution of organic due to negative charge increase<br />

107

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