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

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phase: a) anion replacement to enhance desorption, b) complex<strong>in</strong>g <strong>of</strong> cations b<strong>in</strong>d<strong>in</strong>g<br />

P to release P, c) hydrolysis <strong>of</strong> cations b<strong>in</strong>d<strong>in</strong>g P to release P and d) dissolv<strong>in</strong>g action<br />

<strong>of</strong> acids. Therefore, <strong>the</strong> selection <strong>of</strong> a soil test for P should depend on extract<strong>in</strong>g P<br />

from certa<strong>in</strong> chemical forms <strong>of</strong> <strong>in</strong>terest based on <strong>the</strong> soil characteristics.<br />

Some <strong>the</strong>se methods are reviewed below:<br />

Among <strong>the</strong> use <strong>of</strong> different extractants <strong>the</strong> use <strong>of</strong> water to extract P from soils is<br />

restricted to soils, to which very high amounts <strong>of</strong> P have been added and are present<br />

<strong>in</strong> easily dissolved forms <strong>in</strong> soils. This is not <strong>the</strong> case for <strong>forest</strong> soils <strong>in</strong> general. Only<br />

small amounts <strong>of</strong> soil P can be extracted by water creat<strong>in</strong>g problems <strong>in</strong> chemical<br />

analysis. However despite <strong>the</strong> very low absolute values obta<strong>in</strong>ed by water extraction,<br />

<strong>the</strong>se values relate to <strong>the</strong> <strong>in</strong>tensity parameter <strong>of</strong> P availability <strong>in</strong> soils and have been<br />

used <strong>in</strong> relat<strong>in</strong>g <strong>the</strong>m to capacity parameters <strong>of</strong> soil P obta<strong>in</strong>ed by us<strong>in</strong>g o<strong>the</strong>r methods<br />

(see Ulrich and Khanna 1968). The limitations <strong>of</strong> its wide scale use are both <strong>the</strong><br />

cumbersome extraction procedures to achieve equilibrium solution phases and <strong>the</strong> use<br />

<strong>of</strong> such methods for huge number <strong>of</strong> survey type soil samples.<br />

One <strong>of</strong> <strong>the</strong> most common methods used for <strong>forest</strong> soils is <strong>the</strong> so called Bray method<br />

(Bray and Kurtz 1945). The extractant is a mixture <strong>of</strong> HCl and NH4F, where F acts to<br />

complex <strong>the</strong> Al and Fe and <strong>the</strong> P bound to <strong>the</strong>m is released. The amount <strong>of</strong> acid added<br />

is sometimes varied depend<strong>in</strong>g upon <strong>the</strong> form <strong>of</strong> P to be extracted. The extractant with<br />

low HCl concentration is called <strong>the</strong> Bray1 method. This method is specifically<br />

designed to be used <strong>in</strong> acid soils. Bray 1 and Bray 2 (high HCl concentration)<br />

methods are commonly employed for <strong>forest</strong> soils, especially those with high amounts<br />

<strong>of</strong> organic matter. This method has been used to show short term <strong>changes</strong> <strong>in</strong> <strong>the</strong> soil<br />

due to treatments such as fire (Romanya et al. 1994), soil heat<strong>in</strong>g (Serrasolsas and<br />

Khanna 1995), or fertilizer additions. However, Compton and Cole (1998) reported<br />

that alder stands which had higher P dynamics (uptake, litterfall content, resorption<br />

values) than Douglas fir stands, had lower Bray P value and total P <strong>in</strong> <strong>the</strong> soil,<br />

suggest<strong>in</strong>g that <strong>the</strong> quantification <strong>of</strong> an available P pool alone does not adequately<br />

reflect P supply <strong>in</strong> <strong>forest</strong> stands. When nutrient pools are small, <strong>the</strong> flux through <strong>the</strong>se<br />

pools, must be considered as well to obta<strong>in</strong> a realistic picture <strong>of</strong> nutrient supply from<br />

that pool.<br />

For calcareous and alkal<strong>in</strong>e soils <strong>the</strong> method commonly used employs 0.5 M NaHCO3<br />

solution at a pH <strong>of</strong> 8.5 to extract available soil P (Olsen et al. 1954). This extractant<br />

decreases calcium <strong>in</strong> solution (through precipitation <strong>of</strong> calcium carbonate), and thus<br />

60

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