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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>D. Kirk Nordstrom</dc:contributor>
  <dc:contributor>Judy I. Steiger</dc:contributor>
  <dc:contributor>Briant A. Kimball</dc:contributor>
  <dc:contributor>Philip L. Verplanck</dc:contributor>
  <dc:creator>R. Blaine McCleskey</dc:creator>
  <dc:date>2003</dc:date>
  <dc:description>Water analyses are reported for 259 samples&#13;
collected from the Red River, New Mexico, and its&#13;
tributaries during low-flow(2001) and spring snowmelt&#13;
(2002) tracer studies. Water samples were collected&#13;
along a 20-kilometer reach of the Red River beginning&#13;
just east of the town of Red River and ending at the U.S.&#13;
Geological Survey streamflow-gaging station located&#13;
east of Questa, New Mexico. The study area was&#13;
divided into three sections where separate injections&#13;
and synoptic sampling events were performed during&#13;
the low-flow tracer study. During the spring snowmelt&#13;
tracer study, three tracer injections and synoptic&#13;
sampling events were performed bracketing the areas&#13;
with the greatest metal loading into the Red River as&#13;
determined from the low-flow tracer study. The lowflow&#13;
tracer synoptic sampling events were August 17,&#13;
20, and 24, 2001. The synoptic sampling events for the&#13;
spring snowmelt tracer were March 30, 31, and April 1,&#13;
2002.&#13;
Stream and large inflow water samples were&#13;
sampled using equal-width and depth-integrated&#13;
sampling methods and composited into half-gallon&#13;
bottles. Grab water samples were collected from&#13;
smaller inflows. Stream temperatures were measured at&#13;
the time of sample collection. Samples were&#13;
transported to a nearby central processing location&#13;
where pH and specific conductance were measured and&#13;
the samples processed for chemical analyses. Cations,&#13;
trace metals, iron redox species, and fluoride were&#13;
analyzed at the U.S. Geological Survey laboratory in&#13;
Boulder, Colorado. Cations and trace metal&#13;
concentrations were determined using inductively&#13;
coupled plasma-optical emission spectrometry and&#13;
graphite furnace atomic absorption spectrometry.&#13;
Arsenic concentrations were determined using hydride&#13;
generation atomic absorption spectrometry, iron redox&#13;
species were measured using ultraviolet-visible&#13;
spectrometry, and fluoride concentrations were&#13;
determined using an ion-selective electrode. Alkalinity&#13;
was measured by automated titration, and sulfate,&#13;
chloride, and bromide were analyzed by ion&#13;
chromatography at the U.S. Geological Survey&#13;
laboratory in Salt Lake City, Utah.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.3133/ofr03148</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>U.S. Geological Survey</dc:publisher>
  <dc:title>Questa baseline and pre-mining ground-water quality investigation. 2. Low-flow (2001) and snowmelt (2002) synoptic/tracer water chemistry for the Red River, New Mexico</dc:title>
  <dc:type>reports</dc:type>
</oai_dc:dc>