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<br />Table 1. Distribution of soil-sampling sites by geologic units in townships 01 the Uncompahgre Project area <br />[Numbers under geologic unil indicate the number of sites in each unil within each township; geologic units are defined as follows: <br />Kd. Upper CretaceOus Dakota Sandstone; KIn. Upper Creaaceous Mancos Shale; Qt. Quaternary terrace and alluvial-fan deposits; <br />Qrn. Quaternary (Holocene) alluvium overlying Mancos Shale: Qr. Quaternary (recent) flood-plain alluvium deposited by the <br />Uncompahgre River and other streams; Qd. Quaternary alluvium derived from Dakota Sandstone; --, no samples] <br />Townlhlp Range Geologic unR <br />number Townlhlp (III well) Kd Km Ql am ad <br />(lIg.6) ar <br />I 15 south 96 3 3 3 3 <br />2 15 south 95 3 3 3 3 <br />3 15 south 94 3 3 <br />4 51 north II '4 3 <br />5 51 north 10 3 3 3 3 <br />6 5 t north 09 3 3 <br />7 50 north II 3 3 <br />S 50 north 10 3 3 3 3 <br />9 50 north 09 3 3 <br />10 49 north 10 3 3 3 3 3 <br />II 49 north 09 3 3 3 <br />12 49 north OS 3 3 <br />13 4S north 10 3 'I <br />14 4Snorth 09 3 3 3 <br />15 4Snorth OS 3 3 <br />I Analytical data for all sites included for calculation of geometric means and ranges, but only first three sites ured for analysis of <br />variance (ANOVA). <br />2Analytical data included for calculation of geometric means and ranges, but not for ANOVA. <br /> <br />using tap water, rinsed several times in demineralized <br />water, redried at ambient room temperature, and <br />ground to pass a 2-mm screen in a Wiley mill. Each <br />ground sample was mixed and split, and a part was <br />ashed at 4500C in a muffle furnace for 24 hours. <br />Soils and plant ash were decomposed using a <br />low-temperature mixed acid digestion (Crock and <br />others, 1983). Solutions were analyzed simulta- <br />neously for 40 constituents using inductively coupled <br />plasma atomic-emission spectroscopy (ICP-AES) <br />(Crock and others, 1983). Soils and dried plant <br />material for arsenic and selenium determinations were <br />decomposed by mixed acids and hydrogen peroxide <br />(Crock and others, 1994). Determinations were made <br />by hydride-generation atomic absorption spectroscopy <br />(HGAAS) (Crock and Lichte, 1982; Sanzolone and <br />Chao, 1987). <br />Extractions on soils were done using deionized <br />water (one part soil to five parts water, by weight) by <br />agitation for 16 hours on a horizontal reciprocating <br />shaker (Stewart and others. 1990). Solutions were <br />clarified by centrifugation and filtration (0.45-j!m <br /> <br />filter). Conductivity, pH, and anion concentrations <br />were determined in solution by conductivity meter, <br />standard combination pH electrode, and ion chromato- <br />graph (Wilson and others, 1987; Stewart and others, <br />1990). A part of each solution was predigested to <br />oxidize organic malter, according to a modification <br />developed by Presser and Barnes (1985), prior to <br />arsenic and selenium determination by HGAAS. <br /> <br />Selenium Concentrations <br />in Soils and Alfalfa <br /> <br />The geometric means and ranges for total <br />selenium in all soil samples from the Uncompahgre <br />Project area and in soil samples from each geologic <br />unit (Crock and others, 1994) are listed in table 2. <br />Total-selenium concentrations in the 142 soil samples <br />ranged from 0.1 to 8.6j!glg (table 2). The geometric <br />mean selenium concentration for all soil samples was <br />1.4j!glg, compared to a geometric mean of 0.23 j!g1g <br />for Western soils (Shacklelte and Boerngen, 1984). <br /> <br />18 Detailed StUdy of Selenium and Other Constituents In Water. Bottom Sediment, Soli, Alfalfa, and Biota Associated with <br />Irrigation Drainage In the Uncompahgre Project Area and In the Grand Valley, West-Central Colorado, 1991-93 <br />