Biosolids Decomposition after Surface Applications in West Texas

ABSTRACT In a semiarid environment, climate is a critical factor in the decomposition of surface‐applied biosolids. This study examined the effect of 2‐ to 7‐yr exposure times on the composition of single applications of New York, NY biosolids in western Texas. Exposure time effects on organic matte...

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Veröffentlicht in:Journal of environmental quality 2003-09, Vol.32 (5), p.1773-1781
Hauptverfasser: Jaynes, W. F., Zartman, R. E., Sosebee, R. E., Wester, D. B.
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container_end_page 1781
container_issue 5
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container_title Journal of environmental quality
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creator Jaynes, W. F.
Zartman, R. E.
Sosebee, R. E.
Wester, D. B.
description ABSTRACT In a semiarid environment, climate is a critical factor in the decomposition of surface‐applied biosolids. This study examined the effect of 2‐ to 7‐yr exposure times on the composition of single applications of New York, NY biosolids in western Texas. Exposure time effects on organic matter, N, P, S, Cu, Cr, Pb, Hg, and Zn were studied near Sierra Blanca, TX. Due to organic matter decomposition, total organic C decreased from 340 g kg−1 in fresh biosolids to 180 g kg−1 in biosolids after 82 mo of exposure, whereas the inorganic ash content of the biosolids increased from 339 to 600 g kg−1 Total N decreased from 50 to 10 g N kg−1 and total S decreased from 12 to 6 g S kg−1 Bicarbonate‐available P in the biosolids decreased from 0.9 to 0.2 g kg−1 Successive H2O extractions yielded soluble P concentrations consistent with dicalcium phosphate (dical) for fresh biosolids and tricalcium phosphate (trical) for biosolids exposed for 59 months or more. Sparingly soluble phosphates, such as dical and trical, potentially yield >0.5 mg P L−1 in runoff waters for extended periods after biosolids applications, especially after multiple applications. Selective dissolution of the biosolids indicated that as much as 66 to 78% of P exists as iron phosphates, 16 to 21% as Fe oxides, and 5 to 12% as insoluble Ca phosphates. Chemical analyses of ash samples suggest that Cu and Zn have been lost from biosolids through leaching or runoff and no losses of Pb, Cr, or Hg have occurred since application.
doi_str_mv 10.2134/jeq2003.1773
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F. ; Zartman, R. E. ; Sosebee, R. E. ; Wester, D. B.</creator><creatorcontrib>Jaynes, W. F. ; Zartman, R. E. ; Sosebee, R. E. ; Wester, D. B.</creatorcontrib><description>ABSTRACT In a semiarid environment, climate is a critical factor in the decomposition of surface‐applied biosolids. This study examined the effect of 2‐ to 7‐yr exposure times on the composition of single applications of New York, NY biosolids in western Texas. Exposure time effects on organic matter, N, P, S, Cu, Cr, Pb, Hg, and Zn were studied near Sierra Blanca, TX. Due to organic matter decomposition, total organic C decreased from 340 g kg−1 in fresh biosolids to 180 g kg−1 in biosolids after 82 mo of exposure, whereas the inorganic ash content of the biosolids increased from 339 to 600 g kg−1 Total N decreased from 50 to 10 g N kg−1 and total S decreased from 12 to 6 g S kg−1 Bicarbonate‐available P in the biosolids decreased from 0.9 to 0.2 g kg−1 Successive H2O extractions yielded soluble P concentrations consistent with dicalcium phosphate (dical) for fresh biosolids and tricalcium phosphate (trical) for biosolids exposed for 59 months or more. Sparingly soluble phosphates, such as dical and trical, potentially yield &gt;0.5 mg P L−1 in runoff waters for extended periods after biosolids applications, especially after multiple applications. Selective dissolution of the biosolids indicated that as much as 66 to 78% of P exists as iron phosphates, 16 to 21% as Fe oxides, and 5 to 12% as insoluble Ca phosphates. Chemical analyses of ash samples suggest that Cu and Zn have been lost from biosolids through leaching or runoff and no losses of Pb, Cr, or Hg have occurred since application.</description><identifier>ISSN: 0047-2425</identifier><identifier>EISSN: 1537-2537</identifier><identifier>DOI: 10.2134/jeq2003.1773</identifier><identifier>PMID: 14535320</identifier><identifier>CODEN: JEVQAA</identifier><language>eng</language><publisher>Madison: American Society of Agronomy, Crop Science Society of America, Soil Science Society</publisher><subject>Agronomy. Soil science and plant productions ; Applied sciences ; Biological and medical sciences ; Biosolids ; Calcium phosphates ; Conservation of Natural Resources ; Continental surface waters ; Decomposition ; Desert Climate ; Environmental Monitoring ; Exact sciences and technology ; Fundamental and applied biological sciences. Psychology ; General agronomy. Plant production ; Iron phosphates ; Leaching ; Lead ; Mercury ; Metals, Heavy - analysis ; Natural water pollution ; Organic Chemicals - analysis ; Organic matter ; Other nutrients. Amendments. Solid and liquid wastes. Sludges and slurries ; Pollution ; Refuse Disposal ; Runoff ; Semiarid environments ; Sewage - chemistry ; Soil and water pollution ; Soil Pollutants - analysis ; Soil science ; Soil-plant relationships. Soil fertility. Fertilization. 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F.</creatorcontrib><creatorcontrib>Zartman, R. E.</creatorcontrib><creatorcontrib>Sosebee, R. E.</creatorcontrib><creatorcontrib>Wester, D. B.</creatorcontrib><title>Biosolids Decomposition after Surface Applications in West Texas</title><title>Journal of environmental quality</title><addtitle>J Environ Qual</addtitle><description>ABSTRACT In a semiarid environment, climate is a critical factor in the decomposition of surface‐applied biosolids. This study examined the effect of 2‐ to 7‐yr exposure times on the composition of single applications of New York, NY biosolids in western Texas. Exposure time effects on organic matter, N, P, S, Cu, Cr, Pb, Hg, and Zn were studied near Sierra Blanca, TX. Due to organic matter decomposition, total organic C decreased from 340 g kg−1 in fresh biosolids to 180 g kg−1 in biosolids after 82 mo of exposure, whereas the inorganic ash content of the biosolids increased from 339 to 600 g kg−1 Total N decreased from 50 to 10 g N kg−1 and total S decreased from 12 to 6 g S kg−1 Bicarbonate‐available P in the biosolids decreased from 0.9 to 0.2 g kg−1 Successive H2O extractions yielded soluble P concentrations consistent with dicalcium phosphate (dical) for fresh biosolids and tricalcium phosphate (trical) for biosolids exposed for 59 months or more. Sparingly soluble phosphates, such as dical and trical, potentially yield &gt;0.5 mg P L−1 in runoff waters for extended periods after biosolids applications, especially after multiple applications. Selective dissolution of the biosolids indicated that as much as 66 to 78% of P exists as iron phosphates, 16 to 21% as Fe oxides, and 5 to 12% as insoluble Ca phosphates. Chemical analyses of ash samples suggest that Cu and Zn have been lost from biosolids through leaching or runoff and no losses of Pb, Cr, or Hg have occurred since application.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>Biosolids</subject><subject>Calcium phosphates</subject><subject>Conservation of Natural Resources</subject><subject>Continental surface waters</subject><subject>Decomposition</subject><subject>Desert Climate</subject><subject>Environmental Monitoring</subject><subject>Exact sciences and technology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General agronomy. Plant production</subject><subject>Iron phosphates</subject><subject>Leaching</subject><subject>Lead</subject><subject>Mercury</subject><subject>Metals, Heavy - analysis</subject><subject>Natural water pollution</subject><subject>Organic Chemicals - analysis</subject><subject>Organic matter</subject><subject>Other nutrients. Amendments. Solid and liquid wastes. Sludges and slurries</subject><subject>Pollution</subject><subject>Refuse Disposal</subject><subject>Runoff</subject><subject>Semiarid environments</subject><subject>Sewage - chemistry</subject><subject>Soil and water pollution</subject><subject>Soil Pollutants - analysis</subject><subject>Soil science</subject><subject>Soil-plant relationships. Soil fertility. Fertilization. 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F.</au><au>Zartman, R. E.</au><au>Sosebee, R. E.</au><au>Wester, D. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biosolids Decomposition after Surface Applications in West Texas</atitle><jtitle>Journal of environmental quality</jtitle><addtitle>J Environ Qual</addtitle><date>2003-09</date><risdate>2003</risdate><volume>32</volume><issue>5</issue><spage>1773</spage><epage>1781</epage><pages>1773-1781</pages><issn>0047-2425</issn><eissn>1537-2537</eissn><coden>JEVQAA</coden><abstract>ABSTRACT In a semiarid environment, climate is a critical factor in the decomposition of surface‐applied biosolids. This study examined the effect of 2‐ to 7‐yr exposure times on the composition of single applications of New York, NY biosolids in western Texas. Exposure time effects on organic matter, N, P, S, Cu, Cr, Pb, Hg, and Zn were studied near Sierra Blanca, TX. 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subjects Agronomy. Soil science and plant productions
Applied sciences
Biological and medical sciences
Biosolids
Calcium phosphates
Conservation of Natural Resources
Continental surface waters
Decomposition
Desert Climate
Environmental Monitoring
Exact sciences and technology
Fundamental and applied biological sciences. Psychology
General agronomy. Plant production
Iron phosphates
Leaching
Lead
Mercury
Metals, Heavy - analysis
Natural water pollution
Organic Chemicals - analysis
Organic matter
Other nutrients. Amendments. Solid and liquid wastes. Sludges and slurries
Pollution
Refuse Disposal
Runoff
Semiarid environments
Sewage - chemistry
Soil and water pollution
Soil Pollutants - analysis
Soil science
Soil-plant relationships. Soil fertility. Fertilization. Amendments
Texas
Water Pollutants - analysis
Water treatment and pollution
title Biosolids Decomposition after Surface Applications in West Texas
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