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

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(e) strongly bound occluded Pi forms with<strong>in</strong> sesquioxides by strong HCl; (f) highly<br />

resistant Pi <strong>in</strong> secondary and primary m<strong>in</strong>erals.<br />

The fractionation methods are very widely used with different levels <strong>of</strong> success to<br />

assess P <strong>status</strong> <strong>of</strong> <strong>forest</strong> ecosystems. We present here <strong>the</strong> results <strong>of</strong> three case studies:<br />

(a) Compton and Cole (1998) compared P cycl<strong>in</strong>g between Douglas fir and red alder<br />

stands. Total ecosystem P <strong>in</strong> <strong>the</strong> alder stand was 69% <strong>of</strong> that found <strong>in</strong> <strong>the</strong> Douglas-fir<br />

stand (<strong>in</strong>herit site difference), but <strong>the</strong> alder stand took up 61% more P annually than<br />

Douglas-fir and also showed higher fluxes <strong>of</strong> P <strong>in</strong> litterfall (94%) and resorption<br />

(292%). But all <strong>the</strong> P extractable fractions, which are meant to represent available soil<br />

P, were lower under alder. They came to <strong>the</strong> conclusion that all static measures<br />

(pools) <strong>of</strong> available P do not appear to adequately reflect P supply <strong>in</strong> <strong>the</strong>se <strong>forest</strong><br />

stands.<br />

(b) B<strong>in</strong>kley et al. (2000) <strong>in</strong>vestigated P dynamics <strong>in</strong> Eucalyptus and Albizia pure<br />

species stands, and also <strong>in</strong> 1:1 mixture <strong>of</strong> <strong>the</strong> two species. A P fractionation technique<br />

with a slight modification (Fe impregnated paper) was used <strong>in</strong>stead <strong>of</strong> anion exchange<br />

res<strong>in</strong> to obta<strong>in</strong> easily desorbed P fraction - solution Pi. Eucalyptus had higher<br />

productivity, but both sites had similar amounts <strong>of</strong> P uptake at age 15 yrs. For most Pfractions<br />

<strong>the</strong>re was no effect <strong>of</strong> tree species except HCl-P, which was lower <strong>in</strong> Albizia<br />

than Eucalyptus soil (HCO3-Po was high <strong>in</strong> Albizia soil but NaOH was high <strong>in</strong><br />

Eucalypts). However, solution Pi was high <strong>in</strong> Eucalypts.<br />

(c) Richter et al. (2006) attempted to quantify <strong>changes</strong> <strong>in</strong> P fractions <strong>in</strong> an Ultisol<br />

dur<strong>in</strong>g <strong>the</strong> growth <strong>of</strong> an old-field p<strong>in</strong>e <strong>forest</strong> from 1957-2005. Soil sample were<br />

collected <strong>in</strong> 1962, 1968, 1977, 1982, 1990, 1997, and 2005 and different P fractions<br />

and available P us<strong>in</strong>g <strong>the</strong> Mehlich III method were determ<strong>in</strong>ed. The net transfer <strong>of</strong> P<br />

from m<strong>in</strong>eral soil <strong>in</strong>to tree biomass and O horizons was 82.5 kg ha -1 over a 28 year<br />

period (Table 10). However, this did not dim<strong>in</strong>ish <strong>the</strong> amount <strong>of</strong> labile soil P (anionexchange<br />

res<strong>in</strong>s, and NaHCO3 and Mehlich-III extractants). Substantial decreases <strong>in</strong><br />

slowly cycl<strong>in</strong>g Po and Pi associated with Fe and Al oxides and Ca compounds<br />

occurred dur<strong>in</strong>g 28 years <strong>of</strong> <strong>forest</strong> growth, and <strong>the</strong>se accounted for much <strong>of</strong> <strong>the</strong> P<br />

supplied to biomass and O horizons, show<strong>in</strong>g <strong>the</strong> long-term dynamics <strong>of</strong> P <strong>in</strong> soils as<br />

discussed above (Fig 11 ). Changes <strong>in</strong> soil P are small <strong>in</strong> this aggrad<strong>in</strong>g <strong>forest</strong> (2.9 kg<br />

ha -1 y -1 over 28 yr).<br />

66

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