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assessment of changes in the phosphorus status of forest ...

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enhances <strong>the</strong> dissolution <strong>of</strong> Ca-phosphates. Moreover, this extract<strong>in</strong>g solution<br />

removes dissolved and adsorbed P on calcium carbonate and o<strong>the</strong>r surfaces (Al- and<br />

Fe-oxide). As expected, this method would extract a significant amount <strong>of</strong> organic<br />

matter and thus P associated with it. In recent years, this method has been <strong>in</strong>cluded <strong>in</strong><br />

<strong>the</strong> sequential extraction procedure, where both <strong>the</strong> <strong>in</strong>organic P and organic P forms<br />

extracted by this method are described as readily labile forms. There is very little<br />

evidence to show that <strong>the</strong> organic P fraction extracted by this reagent is readily<br />

m<strong>in</strong>eralisable and can be treated <strong>in</strong> <strong>the</strong> same category as <strong>the</strong> <strong>in</strong>organic P fraction. This<br />

method has been used to detect short-term <strong>changes</strong> <strong>in</strong> <strong>the</strong> amount <strong>of</strong> P <strong>in</strong> <strong>forest</strong> soils.<br />

For example, Bekunda et al. (1990) showed that <strong>changes</strong> <strong>in</strong> <strong>the</strong> amount <strong>of</strong> <strong>in</strong>organic P<br />

ow<strong>in</strong>g to different forms <strong>of</strong> slash management at <strong>the</strong> time <strong>of</strong> plantation establishment<br />

could be measured by <strong>the</strong> NaHCO3 method with good results, though not for organic<br />

P measured <strong>in</strong> <strong>the</strong> extract.<br />

Solutions conta<strong>in</strong><strong>in</strong>g lactate and citrate anions are also extensively used to release P <strong>in</strong><br />

soil test methods. These methods are based on <strong>the</strong> desorption and exchange <strong>of</strong> P from<br />

various soil components. In Germany, Scand<strong>in</strong>avia and many East European<br />

countries different versions <strong>of</strong> <strong>the</strong> lactate method which was suggested by Riehm<br />

(1947) are used. Of <strong>the</strong> two commonly used versions, CAL (calcium lactate and<br />

acetic acid at pH 3.5) dissolves less P than <strong>the</strong> DL (Double lactate) method. The<br />

method extracts comparatively low values <strong>of</strong> P from <strong>forest</strong> soils, when compared to<br />

soils from agricultural land uses, as can be been <strong>in</strong> <strong>the</strong> Fig 13 taken from Le<strong>in</strong>weber<br />

et al. ( 1993). Thus <strong>the</strong> usefulness <strong>of</strong> <strong>the</strong> method to detect small <strong>changes</strong> <strong>in</strong> P <strong>status</strong> <strong>of</strong><br />

<strong>forest</strong>s soils is highly questionable. This method may however be useful for assess<strong>in</strong>g<br />

short term <strong>changes</strong> <strong>in</strong> <strong>forest</strong> soils, eg., after fertilizer additions.<br />

Mehlich used a comb<strong>in</strong>ation <strong>of</strong> HCl and H2SO4 acids (Mehlich 1) to extract P from<br />

soils <strong>in</strong> <strong>the</strong> north-central region <strong>of</strong> <strong>the</strong> U.S. which he modified (Mehlich 1984) to<br />

develop a multi-element extractant. Mehlich 3 extractant is a comb<strong>in</strong>ation <strong>of</strong> acids<br />

(acetic and nitric), salts (ammonium fluoride and ammonium nitrate), and <strong>the</strong><br />

chelat<strong>in</strong>g agent (EDTA). This is a commonly used method, also for <strong>forest</strong> soils <strong>in</strong><br />

parts <strong>of</strong> USA. These methods as <strong>the</strong> o<strong>the</strong>r methods mentioned above provide useful<br />

results for specific short term <strong>changes</strong> <strong>in</strong> P <strong>status</strong>, but as shown by Richter et al.<br />

(2006) this method could not predict <strong>the</strong> long-term amount <strong>of</strong> P taken up by an<br />

aggrad<strong>in</strong>g p<strong>in</strong>e ecosystem.<br />

Use <strong>of</strong> anion exchange res<strong>in</strong> act<strong>in</strong>g as a s<strong>in</strong>k to extract P has been <strong>in</strong> use for a long<br />

time. In recent years an impregnated paper with anion exchange res<strong>in</strong> (Sharpley 2000)<br />

61

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