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  <title><![CDATA[PhD Defense by Jixiang Xu]]></title>
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width="362" height="74"></p><p>&nbsp;</p><p>&nbsp;</p><p>In partial fulfillment of the requirements for the degree of</p><p>&nbsp;</p><p>Master of Science in Biology</p><p>in the</p><p>School of Biological Sciences</p><p>&nbsp;</p><p><strong>Jixiang Xu</strong></p><p><strong>&nbsp;</strong></p><p>Will defend her thesis</p><p>&nbsp;</p><p><strong>“EFFECTS OF SULFOXAFLOR EXPOSURE ON BOMBUS IMPATIENS”</strong></p><p><strong>&nbsp;</strong></p><p><strong>21, July, 2025</strong></p><p>1 PM</p><p><a href="https://gatech.zoom.us/j/98569355573?pwd=KqgRMhQffU7Lrvl6Oh2oKhsEbSdw9v.1">https://gatech.zoom.us/j/98569355573?pwd=KqgRMhQffU7Lrvl6Oh2oKhsEbSdw9v.1</a></p><p>&nbsp;</p><p><strong>&nbsp;</strong></p><p>&nbsp;</p><p><strong>Thesis Advisor:</strong></p><p>Dr. Michael Goodisman</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;</p><p><strong>Committee Members:</strong></p><p>Dr. Joseph Lachance</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;</p><p><strong>&nbsp;</strong>Dr. Annalise Paaby</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;&nbsp;</p><p>Abstract: This study focuses on the insecticide sulfoxaflor (SFX) that reveals that its significant threat to the common eastern bumblebee, Bombus impatiens, is not neurotoxicity but severe reproductive failure. The research hypothesis that chronic, sublethal SFX exposure would negatively impact worker bees by altering gene expression in brain and ovary tissues. While acute toxicity tests established a lethal dose (LC₅₀ of 1.2222 mg/L), the more critical findings came from chronic exposure to field-realistic concentrations (0.16mg/L and 0.31mg/L). These experiments documented severe dose-dependent behavioral and reproductive impairments, including significantly reduced nectar consumption, honey pot construction, and a cessation of egg-laying. RNA sequencing revealed a tissue-specific differential gene expression: while the brain’s gene expression remained largely unaffected, the ovary shows a massive, dose-dependent transcriptomic change. This identifies the ovary, not the brain, as the primary site of chronic SFX pathology. Functional analysis showed SFX disrupting genes essential for meiosis, cellular signaling, energy metabolism, and tissue structure.</p><p>&nbsp;</p>]]></body>
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