Geoffrey Nielsen, Professor Sue Hannaford, Professor Robin Foster

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Presentation transcript:

Relative Dependence of Neural Plasticity on Age and Activity in the Bumblebee (Bombus huntii) Geoffrey Nielsen, Professor Sue Hannaford, Professor Robin Foster University of Puget Sound Biology Department 1500 N. Warner Tacoma, WA 98416 Introduction Neural Plasticity is one of the most fascinating and complex aspects of neuroscience. Due to the complexity of neural plasticity mechanisms, simple models are used to study neural plasticity. The bumblebee, Bombus huntii provides an ideal model organism with which to study neural plasticity, particularly the way it is affected by age and activity1. The Mushroom Body is the portion of the B. huntii brain that is responsible for higher order sensory integration and experience related learning so it will be the focus of this study2. Objective To determine if changes in brain structure in adult worker bumblebees are due to the contributions of age dependent neural plasticity, activity dependent neural plasticity, or a combination of both? Results The prediction that activity rate plays a role in plasticity in the B. huntii brain, is supported by this data. From two sessions of in hive observations, it appears there is no definitive correlation between age and average number of foraging trips per hour (Figure 2). Thus, foraging rate is not a product of age related plasticity and is exhibiting independent effects. Increased activity rate appears to be correlated with a greater ratio of Neuropil to Kenyon cells (Figure 3). As foraging trips per hour increases, The Neuropil volume of B. huntii occupies a larger portion of brain space than Kenyon cell volume. Activity rate seems to be playing a role in the way the B. huntii brain grows and learns, meaning that the activity of the insect is shaping it’s neural development. Figure 2. Foraging trip data for 2 observation sessions. Methods Dissect, slice and mount sections of B. huntii brains on slides. Stain and photograph the mounted sections. Using the program Imagetools, measure the total volume of the Neuropil and Kenyon cells for each brain. Compare volume results to ages and activity levels of bees. Determine if activity rate contributes to changes in structure of B. huntii brain, particularly the ratio of Synapse to cell body in the Mushroom Bodies. Figure 3. Neuropil to Kenyon Cell Ratio as foraging trips per hour increases. Future Research Future research in this area would benefit from a larger sample size to further confirm these results, as well as an attempt to establish the relative contributions that age and activity level have on neural plasticity in B. huntii. Mushroom Bodies References 1.) Farris, Sarah M., Gene E. Robinson, and Susan E. Fahrbach. "Experience and Age Related Outgrowth of Intrinsic Neurons in the Mushroom Bodies of the Adult Worker Bumblebee." The Journal of Neuroscience 21.16 (2001): 6395-404. 2.) Durst, C., S. Eichmueller, and R. Menzel. "Development and Experience Lead to Increased Volume of Subcompartments of the Bumblebee Mushroom Body." Behavioral and Neural Biology 62.3 (1994): 259-63. Acknowledgements Professor Sue Hannaford Professor Robin Foster Preston Van Buren Figure 1. Cross section of the B. huntii brain..