Environmental Science & Technology Theses and Dissertations
Permanent URI for this collectionhttp://hdl.handle.net/1903/2748
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Item Soils Developed in Freshwater Marl Sediments in The Hagerstown (Great) Limestone Valley(1993) Shaw, Joey N.; Rabenhorst, Martin C.; Agronomy; Digital Repository at the University of Maryland; University of Maryland (College Park, MD)Certain calcareous soils occupying alluvial landscape positions in the Hagerstown (Great) limestone valley of western Maryland have developed from highly calcareous ( 60-100g/100g) marl sediments of Holocene age which range in depth from .5m to over 8m. These marlderived soils have a high pH ( 7. 5-8. 5) , low bulk density, and high porosity (0.5 to 0.6). The carbonate in the marl was developed from inorganic and biogenic processes. The marl was formed in now extinct ponds which had inundated alluvial landscape positions during parts of the Holocene period. Certain algae capable of accumulating carbonate internally and externally developed the majority of the marl. Pedogenic processes have transformed the marl sediments into highly calcareous Mollisols. The presence of buried surface horizons and coarse (> fine sand) carbonate forms render classification of these soils problematic. The coarse carbonate forms were mainly biogenic deposits, but these carbonates have been altered sufficiently by coating with pedogenic carbonate to identify calcic horizons. The drainage class is difficult to interpret as a result of the gleyed appearance of the marl sediments (chroma <3) and the high pH of these soils which inhibits Fe oxide reduction. Most of the marl-derived soils (70%) are better drained than the previous classification indicates. These soils have been mapped in the Great Valley in units named for the warners series (fine-silty, carbonatic, mesic Fluvaquentic Haplaquolls) and the Massenet ta series (fine-loamy, carbonatic, mesic, Fluvaquentic Hapludolls). However, proper classification may place these soils in the Typic Calciudolls subgroup. Some soils originally mapped in the very poorly drained Dunning units are very poorly drained marl-derived soils.Item CHROMIUM OXIDATION AND REDUCTION BY HYDROGEN PEROXIDE IN DIVERSE SOILS AND SIMPLE AQUEOUS SYSTEMS(1999) Rock, Melanie Louise; Helz, George R.; James, Bruce R.; Chemistry; Environmental Science & Technology; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)Hydrogen peroxide is being tested for in situ remediation of buried contaminants - either as a direct chemical oxidant in Fenton-type reactions or as a source of oxidizing equivalents in bioremediation. How it affects a common co-contaminant, Cr, is explored here in four chemically diverse high-Cr soils. Soils contaminated with high levels of soluble Cr(VI) from ore processing and soils containing high levels of recently reduced Cr(III) from electroplating waste showed marked increases in chromate after single applications of J-25 mM peroxide. Cr(VI) in the leachates exceeded the drinking water standard (2μM) by 1-3 orders of magnitude. Soluble Cr(III), in the form of dissolved organic complexes, contributed to the likelihood of Cr(III) oxidation. Anaerobic soil conditions at a tannery site prevented oxidation of Cr(III). Naturally occurring Cr in serpentine soil also resisted oxidation. Ambient soluble Cr(VI) in a contaminated aquifer disappeared from peroxide leachates below pH 5, then reappeared as peroxide levels declined. In solutions prepared under environmentally relevant conditions, aged 280 μM Cr(III) treated with 100 μM H2O2 showed increases in Cr(VI) over weeks with maximum oxidation rates achieved in solutions prepared with 2:1 and 4:1 OH^-:Cr. Although Cr(III) speciation differs in fresh and aged aqueous systems, a similar mechanism involving the pre-equilibrium step: Cr(OH)/ + OH- .,. Cr(OH)/ may account for Cr(III) oxidation in both systems. Under alkaline conditions, H2O2 enhanced the oxidative dissolution of Crn(OH)3n^0. The formation of peroxochromium compounds in the presence of H2O2 and Cr(VI) may account for the disappearance and reappearance of Cr(VI) in H2O2 treated soils; as does the possible formation and subsequent reoxidation of Crm\(OH)3n-2^2+ oligomers. Mobilization of hazardous Cr(VI) must be considered in plans to use H2O2 for remediation of chemically complex wastes. Once Cr(III) is oxidized to Cr(VI) by H2O2 it may persist long after applied H2O2 treatments have disappeared. Further, hexavalent Cr will behave as a catalyst toward H20 2 in soils, enhancing its oxidative capacity while helping to dissipate high levels of applied H2O2.Item Soils with Spodic Characteristics on the Eastern Shore of Maryland(1990) Condron, Margaret Anne; Rabenhorst, Martin C.; Environmental Science and Technology; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)A seasonally fluctuating water table may be an important factor in the formation of spodic horizons in sandy, quartzose sediments on the Lower Eastern Shore of Maryland. This study was conducted to examine spodic horizon formation and expression along two topohydrosequences. After a reconnaissance study, two research sites were chosen in the Pocomoke State Forest in Worcester County, Maryland. The soils were classified according to Soil Taxonomy as siliceous, mesic, Typic Quartzipsamments, Aquic Haplorthods, and Aerie and Typic Haplaquods. The spodic horizons were thickest (26-204cm) in the wettest positions. Total organic carbon, pyrophosphateextractable carbon, and extractable aluminum were greatest in the spodic horizons, and there was little extractable iron in the Haplaquods. There was less structural aluminum and potassium in the surface horizons than in the lower horizons. This suggests that feldspar weathering in the surface horizons provides a source of aluminum for the spodic horizon formation. Quantitative estimates of pedogenesis showed net gains of extractable aluminum, total (organic) carbon, and pyrophosphate carbon in the lower landscape positions. The seasonally fluctuating water table appears to influence the movement of soluble organic aluminum complexes through the soil downslope, as well as within the pedon from the surface to subjacent horizons.