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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.W. Metge</dc:contributor>
  <dc:contributor>N. Kinner</dc:contributor>
  <dc:contributor>N. Mayberry</dc:contributor>
  <dc:creator>R.W. Harvey</dc:creator>
  <dc:date>1997</dc:date>
  <dc:description>&lt;div class="hlFld-Abstract"&gt;&lt;div id="abstractBox"&gt;&lt;p class="articleBody_abstractText"&gt;Buoyant densities were determined for groundwater bacteria and microflagellates (protozoa) from a sandy aquifer (Cape Cod, MA) using two methods:  (1) density-gradient centrifugation (DGC) and (2) Stoke's law approximations using sedimentation rates observed during natural-gradient injection and recovery tests. The dwarf (average cell size, 0.3 μm), unattached bacteria inhabiting a pristine zone just beneath the water table and a majority (∼80%) of the morphologically diverse community of free-living bacteria inhabiting a 5-km-long plume of organically-contaminated groundwater had DGC-determined buoyant densities &amp;lt;1.019 g/cm&lt;sup&gt;3&lt;/sup&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;before culturing. In the aquifer, sinking rates for the uncultured 2-μm size class of contaminant plume bacteria were comparable to that of the bromide tracer (1.9 × 10&lt;sup&gt;-&lt;/sup&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;M), also suggesting a low buoyant density. Culturing groundwater bacteria resulted in larger (0.8−1.3 μm), less neutrally-buoyant (1.043−1.081 g/cm&lt;sup&gt;3&lt;/sup&gt;) cells with potential sedimentation rates up to 64-fold higher than those predicted for the uncultured populations. Although sedimentation generally could be neglected in predicting subsurface transport for the community of free-living groundwater bacteria, it appeared to be important for the cultured isolates, at least until they readapt to aquifer conditions. Culturing-induced alterations in size of the contaminant-plume microflagellates (2−3 μm) were ameliorated by using a lower nutrient, acidic (pH 5) porous growth medium. Buoyant densities of the cultured microflagellates were low, i.e., 1.024−1.034 g/cm&lt;sup&gt;3&lt;/sup&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;(using the DGC assay) and 1.017−1.039 g/cm&lt;sup&gt;3&lt;/sup&gt;&lt;span&gt;&amp;nbsp;&lt;/span&gt;(estimated from in-situ sedimentation rates), sug gesting good potential for subsurface transport under favorable conditions.&lt;/p&gt;&lt;/div&gt;&lt;/div&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1021/es960461d</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>ACS</dc:publisher>
  <dc:title>Physiological considerations in applying laboratory-determined buoyant densities to predictions of bacterial and protozoan transport in groundwater: Results of in-situ and laboratory tests</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>