CANOPY MODIFICATION OF PRECIPITATION CHEMISTRY IN DECIDUOUS AND CONIFEROUS FORESTS AFFECTED BY ACIDIC DEPOSITION
Citation
H. Shibata et T. Sakuma, CANOPY MODIFICATION OF PRECIPITATION CHEMISTRY IN DECIDUOUS AND CONIFEROUS FORESTS AFFECTED BY ACIDIC DEPOSITION, Soil Science and Plant Nutrition, 42(1), 1996, pp. 1-10
Categorie Soggetti
Agriculture,"Agriculture Soil Science
SICI code
0038-0768(1996)42:1<1:CMOPCI>2.0.ZU;2-O
Abstract
Ionic concentrations and fluxes of throughfall and precipitation were
measured during a period of 3 y in a deciduous stand (Df-site) and a c
oniferous stand (Cf-site) affected by acidic precipitation in the nort
h-western part of Tomakomai in Hokkaido. Throughfall pH at the Df-site
was higher than precipitation pH in many cases, indicating that the d
eciduous canopy neutralized a proton in acidic precipitation. In contr
ast, pH in throughfall at the Cf-site fluctuated independently of the
acidity of precipitation without any significant difference between pH
in throughfall and that in precipitation. Concentrations of SO42-, K, Na+, Cl- in throughfall were higher than in precipitation at both si
tes, especially during the growing period (from June to October), and
the magnitude of increment at the Cf-site was larger than that at the
Df-site. Na+ and Cl- in net throughfall flux (throughfall flux minus p
recipitation flux) for both sites were markedly affected by sea salt,
while other ions in net throughfall flux were supplied by non sea salt
, namely, external terrestrial, biological and anthropogenic materials
and internal sources of living leaves. Net throughfall flux of proton
s showed that proton consumption on the leaf surface was a major proce
ss of canopy modification. At the Df-site, the absolute value of net H
+ flux during the growing period (from June to October) was almost equ
ivalent to that of K+ and HCO3-, suggesting that the mechanism of H+ c
onsumption during canopy modification was closely dependent upon K+ re
lease from internal sources of foliage and surface reactions which wer
e controlled by bicarbonate and/or weak organic acid equilibrium. Annu
al proton consumption in deciduous and coniferous canopies were 0.53 a
nd 0.28 kmol(c) ha(-1) y(-1) respectively, and these values correspond
ed to about SO and 44% of the proton load as wet deposition, respectiv
ely. The smaller value of proton consumption at the Cf-site compared w
ith the Df-site may reflect the high capturing efficiency of the conif
erous canopy which acts as a collector of dry acidic deposition, espec
ially non sea salt SO42-.