Acid-base chemistry of high-elevation streams in the great smoky mountains
| Autor: | Robert B. Cook, Ralph R. Turner, Mary Anna Bogle, Patrick J. Mulholland, Anthony V. Palumbo, Jerry W. Elwood |
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| Rok vydání: | 1994 |
| Předmět: |
inorganic chemicals
chemistry.chemical_classification Hydrology geography Environmental Engineering geography.geographical_feature_category Base (chemistry) Ecological Modeling Bedrock chemistry.chemical_element STREAMS engineering.material Pollution Nitrogen Sulfur chemistry Environmental chemistry engineering Environmental Chemistry Pyrite Acid–base reaction Leaching (agriculture) Water Science and Technology |
| Zdroj: | Scopus-Elsevier ResearcherID |
| ISSN: | 1573-2932 0049-6979 |
| DOI: | 10.1007/bf01257133 |
| Popis: | Longitudinal and temporal variations in water chemistry were measured in several low-order, high-elevation streams in the Great Smoky Mountains to evaluate the processes responsible for the acid-base chemistry. The streams ranged in average base flow ANC from −30 to 28 μeq L−1 and in pH from 4.54 to 6.40. Low-ANC streams had lower base cation concentrations and higher acid anion concentrations than did the high-ANC streams. NO3 − and SO4 2− were the dominant acid anions. NO3 − was derived from a combination of high leaching of nitrogen from old-growth forests and from high rates of atmospheric deposition. Streamwater SO4 2− was attributed to atmospheric deposition and an internal bedrock source of sulfur (pyrite). Although dissolved Al concentrations increased with decreasing pH in the study streams, the concentrations of inorganic monomeric Al did not follow the pattern expected from equilibrium with aluminum trihydroxide or aluminum silicate phases. During storm events, pH and ANC declined by as much as 0.5 units and 15 μeq L−1, respectively, at the downstream sites. The causes of the episodic acidification were increases in SO4 2− and DOC. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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