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Analysis Methods for the Determination of Anthropogenic Additions of P to Agricultural Soils
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作者 Richard L. Haney Virginia L. jin +4 位作者 Mari-Vaughn V. johnson Elizabeth B. Haney R. Daren Harmel jeffrey G. Arnold michael j. white 《Open Journal of Soil Science》 2015年第2期59-68,共10页
Phosphorus loading and measurement is of concern on lands where biosolids have been applied. Traditional soil testing for plant-available P may be inadequate for the accurate assessment of P loadings in a regulatory e... Phosphorus loading and measurement is of concern on lands where biosolids have been applied. Traditional soil testing for plant-available P may be inadequate for the accurate assessment of P loadings in a regulatory environment as the reported levels may not correlate well with environmental risk. In order to accurately assess potential P runoff and leaching, as well as plant uptake, we must be able to measure organic P mineralized by the biotic community in the soil. Soils with varying rates of biosolid application were evaluated for mineralized organic P during a 112-day incubation using the difference between P measured using a rapid-flow analyzer (RFA) and an axial flow Varian ICP-OES. An increase in the P mineralized from the treated soils was observed from analysis with the Varian ICP-OES, but not with the RFA. These results confirm that even though organic P concentrations have increased due to increasing biosolid application, traditional soil testing using an RFA for detection, would not accurately portray P concentration and potential P loading from treated soils. 展开更多
关键词 Phosphorus ANTHROPOGENIC ADDITIONS Biosolids Rapid-Flow Analyzer (RFA) Inductively Coupled Plasma (ICP) Texas Commission of Environmental Quality (TCEQ) Soil ORGANIC C (SOC) Total N (TN) Water-Soluble ORGANIC C (WSOC) Water Soluble ORGANIC N (WSON)
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Removal of Lithium Citrate from H3A for Determination of Plant Available P
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作者 Richard L. Haney Elizabeth B. Haney +1 位作者 Douglas R. Smith michael j. white 《Open Journal of Soil Science》 2017年第11期301-314,共14页
The soil extractant, H3A, has undergone several iterations to extract calcium (Ca), iron (Fe), aluminum (Al), potassium (K), phosphorus (P), ammonium (NH4-N) and nitrate (NO3-N) under ambient soil conditions. Few soil... The soil extractant, H3A, has undergone several iterations to extract calcium (Ca), iron (Fe), aluminum (Al), potassium (K), phosphorus (P), ammonium (NH4-N) and nitrate (NO3-N) under ambient soil conditions. Few soil extractants currently used by commercial and university soil testing laboratories can perform multi-nutrient extraction without over- or under-estimating at least one nutrient. Soil pH and plant root exudates have a strong influence on nutrient availability and H3A was developed to mimic soil conditions. Lithium citrate was previously used in the H3A formulation, but resulted in a cloudy supernatant in some samples, complicating laboratory analyses. In this study, we removed lithium citrate and compared the nutrients extracted from the modified (H3A-4) to the established (H3A-3) solutions. We found that the new extractant, H3A-4, produced a clear supernatant even in soils with low pH and high iron and aluminum concentrations. H3A-4 accurately predicts plant available nutrients and is a viable choice for commercial and laboratory settings due to its ease of use. 展开更多
关键词 PHOSPHATE SOIL Extraction LITHIUM CITRATE
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