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Sulfur release and retention in forest soil organic matter. [Pseudotsuga menziessii; Alnus rubra Bong]

Thesis/Dissertation ·
OSTI ID:7068275
Sulfur (S) release and retention in decomposing forest litter and humidified soil organic matter were examined in adjacent 55-year-old stands of Douglas-fir (Pseudotsuga menziessii (Mirb.) Franco) and red alder (Alnus rubra Bong). Fresh Douglas-fir and red alder litter had similar concentrations of total S (1220 and 1380 mg S {times} kg{sup {minus}1}, respectively), but the different distribution among four chemical forms (inorganic SO{sub 4}, soluble C-bonded S, ester SO{sub 4}, and insoluble C-bonded S) led to different S losses during decomposition. The initially high mass of inorganic SO{sub 4} was leached from Douglas-fir litter within four months. This resulted in greater S loss than from red alder litter, where insoluble C-bonded S was the major S fraction. Leaching of initially present soluble C-bonded S also contributed significantly to S loss. Concentration of SO{sub 4} (4 vs 0 mg S {times} L{sup {minus}1}) in solutions applied over a one-year period to green Douglas-fir needles decomposing in the forest had no effect on dynamics of insoluble C-bonded S and ester SO{sub 4}. High concentration of SO{sub 4} (32 vs. 0 mg S {times} L{sup {minus}1}) in solutions applied to Douglas-fir needle litter decomposing for 110 days at 22{degree}C resulted in higher insoluble C-bonded S retention only when high concentration of NH{sub 4}NO{sub 3} (112 vs 28 N {times} L{sup {minus}1}) was also in the added solutions. Addition of N alone caused formation of both insoluble organic N and insoluble C-bonded S. Higher initial concentration of insoluble C-bonded S in green needles decomposing in the forest did not affect the S mass remaining after one year. Addition of SO{sub 4} (38 mg S {times} kg soil{sup {minus}1}) to manipulated soil samples from Douglas-fir and red alder A horizons decreased net S mineralization. There was no effect of SO{sub 4} addition on arylsulfatase activity.
Research Organization:
Washington Univ., Seattle, WA (USA)
OSTI ID:
7068275
Country of Publication:
United States
Language:
English