Office of Undergraduate Research

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Emphasizing equitable and inclusive access to research opportunities, the University of Maryland's Office of Undergraduate Research (OUR) empowers undergraduates and faculty to engage and succeed in inquiry, creative activity, and scholarship. This collection includes materials shared by undergraduate researchers during OUR events. It also encompasses materials from Undergraduate Research Day 2020, Undergraduate Research Day 2021, and Undergraduate Research Day 2022, which were organized by the Maryland Center for Undergraduate Research.

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Author: search.filters.author.Riggins, TracySubject: search.filters.subject.Psychology

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    Exploring the Impact of Prenatal Drug Exposure on Brain Development: Data Collection Framework
    (2024) Sare, Perfect; Jones, Morgan; Chi, Zehua; Riggins, Tracy
    Understanding brain development is a critical area of neuroscience requiring comprehensive research. Numerous factors, including prenatal drug exposure (PDE), significantly influence both pre- and postnatal brain development. The HEALthy Brain and Child Development (HBCD) Study is a longitudinal study that aims to explore these impacts and advance our knowledge of early brain and child development. It utilizes multiple, carefully curated methods to obtain physiological data from participants, including diverse patient recruitment, biospecimen collection, and various MRI scans. This poster will address these methods of data collection and how they will contribute to future research. 2
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    Relations between amygdala:hippocampus ratios and depressive symptoms in typically developing 4- to 8-year-old children
    (2020) Coley, Katherine; Turcios, Miguel; Weinberg, Benjamin; Riggins, Tracy; Riggins, Tracy
    Previous literature suggests that the coordination between the amygdala and hippocampus, regions critical for encoding of complex memory and emotion, are associated with depression and risk factors for depression, such as negative memory bias, during adulthood (Yavas et al., 2019; Gerritsen et al., 2012). Research on adolescents ages 8-17 suggests that increased amygdala:hippocampus ratios are related to the severity of anxiety in pediatric major depression (MacMillan et al., 2003). Although associations between amygdala:hippocampus ratios and depression are well-documented in older samples, these associations are not well-explored in early childhood (i.e., <8 years). Given this is a developmental period during which both the amygdala and the hippocampus undergo structural and functional changes (Riggins et al., 2018; Stern et al., 2019), it may be especially important to understand how these developmental changes relate to depressive symptoms in early childhood. The present research aims to address this gap in the literature. Specifically, we examined depressive symptoms and amygdala:hippocampus ratios in typically developing 4- to 8-year-old children drawn from a larger, longitudinal study on brain development in early childhood (N=200, 100 female; Riggins et al., 2018). Depression scores were assessed using the Children’s Depression Inventory (CDI; Kovacs, 1985). Brain region volumes were collected using a standard resolution (.9mm3), T1-weighted whole brain structural magnetic resonance imaging (MRI) scan and processed using FreeSurfer (v5.1). In addition to amygdala and hippocampal volumes, intracranial volume (ICV) was collected as a control for participant head size. Analysis using partial correlations revealed a significant association between total amygdala:hippocampus ratios and depressive symptoms, r(50) = -.234, p = .048. The association between right amygdala:hippocampus ratios and depressive symptoms approached significance, r(50) = -.218, p = .060, and the association between left amygdala:hippocampus ratios and depressive symptoms were not significant. Contrary to previous research, smaller amygdala:hippocampus ratios predicted increased depressive symptoms. Implications for this research are discussed further.
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    Exploring Hippocampal Structural Differences in Habitual vs Non-habitual Nappers During Early Childhood
    (2020) Meredith, Lena; Allard, Tamara; Riggins, Tracy; Riggins, Tracy
    During sleep, memories become less vulnerable to interference, both during overnight sleep and naps. Previous research in adults suggests this effect is partially due to a “transfer” of memories from hippocampus to cortex, but there is little research investigating this process in children. Existing literature suggests habitually napping children need naps more than non-habitually napping children because their hippocampus is less mature. This study examines the relation between habitual versus non-habitual nappers and the hippocampus in early childhood. The participants are part of a larger ongoing study, from which we had 21 participants (Mage= 4.49 years, SD=0.51, 9 female). Of the 21 participants, 8 were nappers (napped 5+ days/week) and 13 were non-nappers (napped <5 days/week). Hippocampal volumes were extracted from T1 weighted MRI scans via FreeSurfer 6.0.0 and refined with a Segmentation Adapter Tool (Morey et al., 2009). Subregions of hippocampal head, body, and tail were identified via standard anatomical landmarks (Watson et al., 1992; Weiss et al., 2005). Preliminary analyses examined possible confounding differences between groups (age, sex, and intercranial volume). There were no differences, thus these measures were not controlled for. Results showed significant differences in hippocampal tail volumes. In the left hemisphere, nappers had larger volumes than non-nappers. Although these are preliminary results, the findings support that variation in hippocampal development may relate to nap status in developing children. Future research will focus on increased sample sizes and investigate other brain regions to determine the specificity of these effects.