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
Citations number
18
Categorie Soggetti
Agriculture,"Agriculture Soil Science
ISSN journal
00380768
Volume
42
Issue
1
Year of publication
1996
Pages
1 - 10
Database
ISI
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-.