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<br />Chemical and isotopic data indicate that bed <br />sediments in the upper reaches of the study area <br />were a source of ammonium to the small-area flow <br />system. For example. chemical and isotopic analy- <br />ses of dissolved ammonium in ground water below <br />the sediment/water interface at McKay Road on <br />November 2, 1992, represent ammonium production in <br />'the sediments under the river at this site (fig. 18). <br />Ammonium concentrations were higher at a depth of <br />12 in. below the sediment/water interface than at other <br />sampled depths, and the l)lsN composition of the <br />ammonium at a depth of 12 in. was about 9 to 12 per <br />mil lighter than the l)lsN composition of ammonium at <br />other depths (table 6). Ammonium produced in-situ <br />generally is isotopically lighter than ammonium that <br />has been transported and subjected to reactions like <br />nitrification that cause the residual ammonium to <br />become isotopically enriched. Although the hydraulic- <br />head difference at the time of measurement was <br />directed from the river into the sediments, indicating no <br />advective flux to the river of ammonium at the 12-in <br />depth, the 24-hour data indicate that an upward flux of <br />ammonium sometime during the day was likely. The <br />relatively high organic-matter contentofbed sediments <br />at McKay Road indicates that the ammonium probably <br />was derived from the mineralization of organic nitro- <br />gen in sedimentary organic matter. The concentration <br />of orthophosphate in ground water below the sediment! <br />water interface also was higher at a depth of 12 in. than <br />at other sampled depths on the same date. indicating <br />that the mineralization of organic matter may have pro- <br />vided dissolved phosphorus to the small-area flow sys- <br />tem. <br />Sedimentary organic matter probably was <br />the source of high concentrations of dissolved ammo- <br />nium and orthophosphate in ground water beneath the <br />river at cross-section site 6 (table 9). At this site, the <br />sedimentary organic matter may have been excrement <br />from waterfowl (table 6). This reach of the river was <br />densely populated by waterfowl during the fall. The <br />nitrogen-isotope composition of ammonium in ground <br />water at the site on December 22. 1992, was the same <br />as the isotopic composition of fresh waterfowl excre- <br />ment (table 6). The isotopic composition of ammo- <br />nium in weathered waterfowl excrement was about <br />4 per mil heavier than that in the fresh material, indicat- <br />ing that the ammonium in the weathered material <br />had mineralized and lost isotopically light nitrogen. <br />Although there was not a net discharge of ground <br />water to the river at site 6 at the time of sampling on <br /> <br />December 22, 1992 (table 9), hydraulic head at the <br />piezometer from which the isotope sample was col- <br />lected was higher than the head in the river. <br /> <br />In addition to the bed sediments being sources <br />of dissolved-nitrogen species to ground water in <br />the small-area flow system, they also were sinks for <br />dissolved-nitrogen species. The combination of <br />low DO concentrations in ground water below the <br />sediment!water interface and the presence of nitrate <br />provided suitable conditions for denitrification to occur <br />in the small-area flow system. Laboratory incubations <br />indicated a measurable potential for denitrification in <br />the bed sediments (table 7). Rates of denitrification <br />(as indicated by N20 production) in riverbed sediments <br />from 88th Avenue and McKay Road sites increased <br />substantially when nitrate concentrations in pore water <br />in those sediments were increased from low in-situ <br />values, whereas the increase in denitrification rate in <br />sediments from Road 8 site was much smaller when <br />nitrate concentratiQns were increased from high in-situ <br />values. These results indicate that (1) denitrification <br />rates in bed sediments from 88th Avenue and McKay <br />Road sites were more limited by the availability of <br />nitrate than denitrification rates in sediments from <br />Road 8 site; and (2) any nitrate entering bed sediments <br />in the vicinity of 88th Avenue or McKay Road sites, <br />3 to 6 mi. downstream from the MWRD, would proba- <br />bly be reduced to N2, which is consistent with the low <br />concentrations of dissolved nitrite plus nitrate in <br />ground water from the small-area flow system at those <br />sites (fig. 17). Rates of denitrification in sediments <br />from the Henderson and Road 8 sites increased propor- <br />tionally more than denitrification rates in sediments <br />from 88th Avenue and McKay Road sites when glucose <br />was added to the sediments, which indicates that <br />denitrification rates in riverbed sediments from the <br />Henderson and Road 8 sites were more limited by the <br />availability of organic carbon than denitrification rates <br />in sediments from the 88th Avenue and McKay Road <br />sites. This interpretation is consistent with measure- <br />ments of organic-matter content that indicated a larger <br />percentage of organic matter in riverbed sediments <br />from the McKay Road site than in sediments from the <br />Henderson or Road 8 sites (table 5). In general, the <br />presence of a denitrifying potential in sediments in the <br />small-area flow system indicates that the small-area <br />flow system could be a sink for nitrate in ground water <br />from the large-area flow system and for nitrate in river <br />water. <br /> <br /> <br /> <br />32 Quantity and Quality of Ground-Water Dlscharga to the South Platte Rlvar, Denver to Fort Lupton, Colorado, <br />AUgU8t1992 Through July 1993 <br />