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Office of Undergraduate Research Home » 2020 Undergraduate Research Symposium Schedules

Found 6 projects

Oral Presentation 3

2:45 PM to 4:15 PM
“We Pieced This Country Together”: A Visual and Multimedia Story Board
Presenter
  • Kim Anh (Kim) Tran, Senior, Public Health-Global Health Mary Gates Scholar
Mentor
  • LaShawnDa Pittman, American Ethnic Studies
Session
    Session O-3B: Using a Race Equity and Social Justice Lens to Support Vulnerable Populations
  • 2:45 PM to 4:15 PM

  • Other American Ethnic Studies mentored projects (2)
  • Other students mentored by LaShawnDa Pittman (1)
“We Pieced This Country Together”: A Visual and Multimedia Story Boardclose

There is a long-standing concern that in American society, historical roots, structural racism, and systems of power have perpetuated the spectrum of negative health outcomes in communities of color. As the status quo is maintained, policy and public opinion reflect the continual oppression of minority families. Through my research, I created a visual and multimedia project that will identify the relationship between public policy and the social determinants of health, and how these factors have affected different communities of color within Washington state and the national level. I conducted extensive library research, analyzed and interpreted data, and utilized GIS technologies to visualize the placement of different communities. This work includes identifying historical background information, past U.S. policies, and relevant literature. In this visual and multimedia project, I displayed four puzzle pieces representing different communities (Asian, Native American, Hispanic, and African Americans) on a map, and examined public policies implemented by European colonizers that racialized minorities in unique ways. This chronological project displayed contemporary policies in housing, economic, employment, education, and criminal justice. Overall, I looked at each group's distinct experience of racial health disparities and will use this platform for dialogue to emerge for students and community members on these topics to prioritize the needs, barriers and solutions to confront racism.


MJ60 Krypton Campaign 3 Data Analysis
Presenter
  • Madison R. Durand, Senior, Physics: Comprehensive Physics, Astronomy NASA Space Grant Scholar
Mentor
  • Jason Detwiler, Physics
Session
    Session O-3I: Neutrinos, Planets, Stars and Galaxies
  • 2:45 PM to 4:15 PM

  • Other Physics mentored projects (33)
  • Other students mentored by Jason Detwiler (1)
MJ60 Krypton Campaign 3 Data Analysisclose

The MAJORANA experiment and its follow-on, the Large Enriched Germanium Experiment for Neutrinoless Double-Beta Decay (LEGEND), search for the creation of matter in the form of neutrinoless double-beta decay, a process that would demonstrate that neutrinos are their own antiparticle and that lepton number conservation may be violated, allowing a deeper understanding of the matter-antimatter imbalance in the universe. MJ60 is a germanium detector used to investigate the low-energy region of the MAJORANA DEMONSTRATOR data, as well as the waveforms produced from incident betas in comparison with gamma events. The latter of these is important for understanding the background of LEGEND: the detectors are submerged in liquid argon, in which beta decays of argon-39 and argon-42 contribute to the background of the extremely sensitive experiment. MJ60 was originally a prototype for the P-type point-contact detectors used in the MAJORANA DEMONSTRATOR. Our group is using this detector to measure mechanisms of energy loss near the detector surfaces by recording events from the nearly monoenergetic beta emissions of metastable krypton-83 (83Kr) at 18 and ~30 keV. Analysis of the waveforms produced from these events, which has been my primary task, will allow us to investigate whether betas incident on our detectors’ passivated surface exhibit markedly different charge collection than gammas, as has been hypothesized. If this expectation is upheld, we will be able to produce a method to identify these events based upon a calculated parameter from the recorded waveforms. Such a parameter will help inform future detector R&D efforts, and will also contribute to background rejection capabilities in MAJORANA and LEGEND.


Characterizing 100+ Neutrino Detectors for the COHERENT Experiment
Presenter
  • Olivia Wilde McGoldrick, Senior, Physics: Comprehensive Physics UW Honors Program
Mentor
  • Jason Detwiler, Physics
Session
    Session O-3I: Neutrinos, Planets, Stars and Galaxies
  • 2:45 PM to 4:15 PM

  • Other Physics mentored projects (33)
  • Other students mentored by Jason Detwiler (1)
Characterizing 100+ Neutrino Detectors for the COHERENT Experimentclose

The COHERENT experiment is endeavoring to detect Coherent Elastic Neutrino-Nucleus Scattering (CEνNS) in several nuclear targets using the Spallation Neutron Source (SNS) at Oak Ridge National Laboratory (ORNL). We search for very low energy (on the order of keV) coherent interactions between neutrinos and atomic nuclei using an array of particle detectors made of different scintillating materials. Neutrinos are fundamental particles under the Standard Model of particle physics that historically have not conformed to theoretical expectations. Understanding their interactions with other particles helps us potentially find other unexpected qualities of neutrinos and in that, discover new physics. At the UW component of the COHERENT team, I along with several other physics undergrads, have just finished characterizing over one-hundred NaI(Tl) crystals to contribute to a large array of detectors at ORNL where they will be illuminated by a strong, pulsed flux of neutrinos born from pions and muons generated in the SNS beam target. For each crystal, I used two characteristic radioactive sources (133Ba & 137Cs) to gather data on each crystal for characterization of their use at ORNL. Each crystal was run for 1.67 hours to find the optimal operating voltage (gain) and to explore the energy linearity of radiation detections at different points in each 7kg crystal (this allowed us to identify if the crystals had any cracks that would interfere with detections). In this talk, I intend to present the statistics on the measured crystal characteristics, including gains, energy resolution, scintillation uniformity as we prepare to ship the crystals to ORNL for installation in the array of other detectors capable of detecting the CEνNS phenomenon.


Poster Presentation 7

2:40 PM to 3:25 PM
Mothering During Jim Crow: Using the Reproductive Justice Framework to Understand Black Motherhood During Legalized Racism
Presenters
  • Ayan Hussein (Ayan) Mohamed, Senior, Public Health-Global Health
  • Rina Yan, Senior, Public Health-Global Health
  • Alana Tida (Alana) Lim, Senior, Microbiology
  • Rachel Brenda (Rachel) Vulk, Senior, Environmental Science & Resource Management
  • Mia Grace Schuman, Senior, Gender, Women, and Sexuality Studies
  • Anthony Chung, Sophomore, Engineering Undeclared
Mentor
  • LaShawnDa Pittman, American Ethnic Studies
Session
    Session T-7A: Culture, Race and Equity, Immigration
  • 2:40 PM to 3:25 PM

  • Other American Ethnic Studies mentored projects (2)
  • Other students mentored by LaShawnDa Pittman (1)
Mothering During Jim Crow: Using the Reproductive Justice Framework to Understand Black Motherhood During Legalized Racismclose

Jim Crow era legalized racism denied Black women the freedom to exercise control over their childbearing and childrearing; specifically, by restricting their access to necessary medical care and sufficient resources to care for their families, and by constraining their autonomy and agency. As a consequence, Black women experienced uniquely poor reproductive health and family outcomes compared to all other racial and ethnic groups (Eichelberger et al. 2016); these racial disparities persist today. This study applies a reproductive justice framework to understanding Black women’s lived experiences of systematic raced and gendered oppression, as well as their forms of resistance when caring for themselves and their children. Reproductive justice is the personal right to control one’s body, have children under the conditions that we choose, and parent those children in stable communities (Sister Song 1997). Thus, we ask how did gendered racism impact Black women’s experiences of reproductive justice and what strategies of resistance did they devise in response? We used Dedoose, a cloud-based mixed methods software, to conduct a content analysis of oral histories from two oral history repositories. These primary sources were excerpted and coded for common themes including racism’s influence on childbearing and childrearing, socioeconomic experiences, access to medical care, and protective factors. We have three preliminary findings that contribute to existing literature: 1) when women required more medical care than midwives could provide, they experienced numerous barriers to accessing such care, 2) Black women experienced multiple levels of social control that undermined their childrearing, and 3) women devised strategies of resistance to care for their bodies and their children, including collective childrearing, resource sharing, and instilling a sense of self-worth in their children.


A Genetic Screen for Suppressors of IPMK-1 in C. elegans
Presenter
  • Megan Lee, Senior, Spanish, Biochemistry UW Honors Program
Mentors
  • Matt Kaeberlein, Pathology
  • Jason Pitt,
Session
    Session T-7E: Neuroscience 2
  • 2:40 PM to 3:25 PM

  • Other Pathology mentored projects (31)
  • Other students mentored by Matt Kaeberlein (16)
  • Other students mentored by Jason Pitt (1)
A Genetic Screen for Suppressors of IPMK-1 in C. elegansclose

The hypoxia response pathway, induced by genetic activation or by decreasing oxygen available, has been shown to extend the lifespan of C. elegans. A previous experiment conducted in our lab compared the transcriptomes of worms treated with normoxia, continuous hypoxia, and intermittent hypoxia therapy (IHT). This study showed that IHT doubles lifespan in C. elegans and was partially controlled by the enzyme inositol polyphosphate multikinase (IPMK-1), which suppresses some of the lifespan extension benefits of IHT. To further explore the genetic basis for the effect of IPMK-1 on IHT, we performed a forward genetic suppressor screen on the IPMK-1 animals. IPMK-1 animals die at elevated temperature so we mutagenized IPMK-1(sea9) worms and selected animals from the F2 generation that reached adulthood at 26.5oC. Identifying the genetic changes in these suppressors will tell us more about the control of IHT and how it promotes longevity.


Poster Presentation 8

3:30 PM to 4:15 PM
Using Circularly Permuted GFP to Visualize Dynamic ATP Levels in C. elegans Throughout Aging
Presenter
  • Brendon Eugene Michael Davis, Senior, Mathematics, Biology (Molecular, Cellular & Developmental) Mary Gates Scholar, UW Honors Program
Mentors
  • Matt Kaeberlein, Pathology
  • Jason Pitt,
Session
    Session T-8G: Medicine, Pathology
  • 3:30 PM to 4:15 PM

  • Other Pathology mentored projects (31)
  • Other students mentored by Matt Kaeberlein (16)
  • Other students mentored by Jason Pitt (1)
Using Circularly Permuted GFP to Visualize Dynamic ATP Levels in C. elegans Throughout Agingclose

A 2019 study by Lobas, et al. demonstrated that a circularly permuted form of Green Fluorescent Protein (GFP) can be created such that it only fluoresces when bound to adenosine 5’ triphosphate (ATP), thereby acting as an observable ATP sensor. The primary source of ATP production in cells is in the mitochondria, and loss of mitochondrial function is considered a hallmark of aging. Because ATP additionally reflects the energetic availability of tissue in multicellular animals, it is of interest to study how ATP levels change in an organism throughout aging and in response to environmental stressors. This study uses a novel plasmid construct that has been optimized to express the fluorescent ATP sensor in the nematode C. elegans. These nematodes are visualized using our fluorescent imaging robot to measure ATP levels throughout the whole lifetime of the worms in order to determine if cellular ATP levels serve as an aging biomarker. The first construct uses whole body expression of the ATP sensor, which is expected to show varying levels of ATP-reporting fluorescence throughout the life of each animal before darkening in response to age-induced paralysis and death. Subsequent studies employ different promoters in the plasmid to create tissue-specific fluorescence. This allows for a wide combination of experiments that test the effect of environmental, temporal, and genetic factors on specific tissue ATP levels and longevity in C. elegans. For example, expressing the ATP sensor in hepatocytes in organisms under cyanide conditions indicates the energetic response of these cells to toxin. Results from these follow-up studies indicate how cellular energy affects organisms’ lifespans and the ability to respond to stressors, as well as the role that varying biochemical pathways play in maintaining energetic homeostasis during aging.


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