Areal activities and stratification of hydrolytic enzymes involved in the biochemical cycles of carbon, nitrogen, sulphur and phosphorus in podsolized boreal forest soils

• Published in: Soil biology & biochemistry 2004-03, Vol.36 (3), p.425-433
• Main Authors: Wittmann, Christoph, Kähkönen, Mika A., Ilvesniemi, Hannu, Kurola, Jukka, Salkinoja-Salonen, Mirja S.
• Format: Article
• Language: English
• Subjects: Abies; Agronomy. Soil science and plant productions; Biochemistry and biology; biogeochemical cycles; Biological and medical sciences; Boreal forest; boreal forests; carbon; Chemical, physicochemical, biochemical and biological properties; coniferous forests; Enzyme activity; forest soils; Fundamental and applied biological sciences. Psychology; nitrogen; phosphorus; Physics, chemistry, biochemistry and biology of agricultural and forest soils; Picea abies; Pinus sylvestris; Seasonal distribution; Soil enzymes; soil pH; Soil science; sulfur; Vertical distribution
• ISSN: 0038-0717; 1879-3428
• DOI: 10.1016/j.soilbio.2003.10.019

A novel approach allowing on-site high throughput enzyme activity measurements by fluorogenic model substrates was applied to study the functioning of enzymes involved in biochemical cycling of nutrients in boreal forest soil ecosystems. The examined enzymes comprised α-glucosidase, β-glucosidase, β-xylosidase, β-cellobiosidase, N-acetyl-glucosamidase, acetate-esterase, butyrate-esterase, phosphomonoesterase, sulphatase and aminopeptidase, whereby spatial and seasonal variation of their activity was investigated over nine seasons in 2 years. The studied sites of boreal podzolized soil of Pinus sylvestris and Picea abies forest were located in central Finland. Activity of all enzymes except sulphatase was highest in the humus layer in all seasons. Maximum sulphatase activity was located below the humus layer in the soil column. Annual activities of acetate-esterase, butyrate-esterase, β-glucosidase and phosphomonosterase calculated to in situ temperature during the year were 480–700, 690–950, 110–190 and 110–200 mol m −2 year −1, respectively. They were up to 100 fold higher than the other six measured activities. The overall turnover capacity of the enzymes was >1000 mol of ester linked carbon, >700 mols carbon from different carbohydrates, 100–200 mol of ester linked phosphate, 10–40 mol of ester linked sulphate m −2 year −1. Winter time (November–April) contributed from 7 to 32% to the annual turnover capacity indicating important enzyme activities also during a cold period of the year. Clear-cutting of the tree stand did not adversely affect enzyme activities related to the cycling of carbon, nitrogen, sulphur and phosphorus during the year. The pH optimum for hemicellulose and cellulose hydrolysing enzymes was pH 3–4 and the pH optimum of phosphomonoesterase, sulphatase, aminopeptidase and N-acetyl-glucosamidase was 4–5. This shows that the hydrolytic activities were adapted to the acid pH-values of the soils. The soil hydrolytic potential was many fold higher as compared to the actual amount of litter it received in the P. sylvestris and P. abies forests.