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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>Kerry L. Weber</dc:contributor>
  <dc:contributor>Todd J. Severson</dc:contributor>
  <dc:contributor>Theresa M. Schreier</dc:contributor>
  <dc:contributor>Denise A. Mayer</dc:contributor>
  <dc:contributor>Douglas B. Aloisi</dc:contributor>
  <dc:contributor>Nathan L. Eckert</dc:contributor>
  <dc:creator>James A. Luoma</dc:creator>
  <dc:date>2015</dc:date>
  <dc:description>&lt;p&gt;The study was completed to evaluate the exposure-related effects of a biopesticide for dreissenid mussel (&lt;i&gt;Dreissena polymorpha&lt;/i&gt;, zebra mussel and&amp;nbsp;&lt;i&gt;Dreissena rostriformis bugensis&lt;/i&gt;, quagga mussel) control on glochidia from unionid mussels endemic to the Great Lakes and Upper Mississippi River Basins. The commercially prepared biopesticide was either a spray-dried powder (SDP) or freeze-dried powder (FDP) formulation of&amp;nbsp;&lt;i&gt;Pseudomonas fluorescens&lt;/i&gt;, strain CL145A. Glochidia of the unionid mussel species&amp;nbsp;&lt;i&gt;Lampsilis cardium&lt;/i&gt;,&amp;nbsp;&lt;i&gt;Lampsilis siliquoidea&lt;/i&gt;,&lt;i&gt;Lampsilis higginsii&lt;/i&gt;,&amp;nbsp;&lt;i&gt;Ligumia recta&lt;/i&gt;,&amp;nbsp;&lt;i&gt;Obovaria olivaria&lt;/i&gt;, and&amp;nbsp;&lt;i&gt;Actinonaias ligamentina&lt;/i&gt;&amp;nbsp;were exposed to SDP-formulated&amp;nbsp;&lt;i&gt;P. fluorescens&lt;/i&gt;&amp;nbsp;and&lt;i&gt;Lampsilis cardium&lt;/i&gt;&amp;nbsp;and&amp;nbsp;&lt;i&gt;Megalonaias nervosa&lt;/i&gt;&amp;nbsp;were exposed to FDP-formulated&amp;nbsp;&lt;i&gt;P. fluorescens&lt;/i&gt;.&lt;/p&gt;
&lt;p&gt;All exposures were static, 24 hours in duration, and included six treatment groups. The treatment groups included (1) an untreated control, (2) a positive control which received a nominal target active ingredient (AI) concentration of 300 milligrams per liter (mg/L) of heat-deactivated test article, and (3) treatments that received nominal target AI concentrations of 50, 100, 200, and 300 mg/L of test article. All treatment concentrations are reported based on active ingredient.&lt;/p&gt;
&lt;p&gt;Glochidia viability was reduced in two of the six species exposed to 50 mg/L SDP and in four of the six species exposed to 100 mg/L SDP when compared to untreated control groups at 6, 12, and 24 hours. Regardless of sample time, concentrations of 200 and 300 mg/L of SDP and 300 mg/L of heat-deactivated SDP (positive control) substantially reduced glochidia viability in all species except,&amp;nbsp;&lt;i&gt;L&lt;/i&gt;.&amp;nbsp;&lt;i&gt;higginsii&lt;/i&gt;. Glochidia viability was only reduced for L. cardium exposed to FDP at concentrations &amp;ge; 200 mg/L. After 24 hours of FDP exposure, differences in glochidia viability were only detected in&amp;nbsp;&lt;i&gt;M&lt;/i&gt;.&amp;nbsp;&lt;i&gt;nervosa&lt;/i&gt;&amp;nbsp;that were exposed to 300 mg/L of heat-deactivated SDP. However, given the low viability in the control group, the results for&amp;nbsp;&lt;i&gt;M&lt;/i&gt;.&amp;nbsp;&lt;i&gt;nervosa&lt;/i&gt;&amp;nbsp;should be interpreted with caution.&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.3133/ofr20151094</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>U.S. Geological Survey</dc:publisher>
  <dc:title>Exposure-related effects of formulated &lt;i&gt;Pseudomonas fluorescens&lt;/i&gt; strain CL145A to glochidia from seven unionid mussel species</dc:title>
  <dc:type>reports</dc:type>
</oai_dc:dc>