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Description
When a rolling ball exits a spiral tube, it typically maintains its final inertial state and travels along straight line in concordance with Newton's first law of motion. Yet, most people predict that the ball will curve, a "naive physics" misconception called the curvilinear impetus (CI) bias. In the current

When a rolling ball exits a spiral tube, it typically maintains its final inertial state and travels along straight line in concordance with Newton's first law of motion. Yet, most people predict that the ball will curve, a "naive physics" misconception called the curvilinear impetus (CI) bias. In the current paper, we explore the ecological hypothesis that the CI bias arises from overgeneralization of correct motion of biological agents. Previous research has established that humans curve when exiting a spiral maze, and college students believe this motion is the same for balls and humans. The current paper consists of two follow up experiments. The first experiment tested the exiting behavior of rodents from a spiral rat maze. Though there were weaknesses in design and procedures of the maze, the findings support that rats do not behave like humans who exhibit the CI bias when exiting a spiral maze. These results are consistent with the CI bias being an overgeneralization of human motion, rather than generic biological motion. The second experiment tested physics teachers on their conception of how a humans and balls behave when exiting a spiral tube. Teachers demonstrated correct knowledge of the straight trajectory of a ball, but generalized the ball's behavior to human motion. Thus physics teachers exhibit the opposite bias from college students and presume that all motion is like inanimate motion. This evidence supports that this type of naive physics inertial bias is at least partly due to participants overgeneralizing both inanimate and animate motion to be the same, perhaps in an effort to minimize cognitive reference memory load. In short, physics training appears not to eliminate the bias, but rather to simply shift it from the presumption of stereotypical animate to stereotypical inanimate behavior.
ContributorsDye, Rosaline (Author) / Mcbeath, Michael K (Thesis advisor) / Sanabria, Federico (Committee member) / Megowan, Colleen (Committee member) / Arizona State University (Publisher)
Created2013
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Description
Smoking remains the leading cause of preventable death in the United States, and early initiation is associated with greater difficulty quitting. Among adolescent smokers, those with attention-deficit hyperactivity disorder (ADHD), characterized by difficulties associated with impulsivity, hyperactivity, and inattention, smoke at nearly twice the rate of their peers.

Smoking remains the leading cause of preventable death in the United States, and early initiation is associated with greater difficulty quitting. Among adolescent smokers, those with attention-deficit hyperactivity disorder (ADHD), characterized by difficulties associated with impulsivity, hyperactivity, and inattention, smoke at nearly twice the rate of their peers. Although cigarette smoking is highly addictive, nicotine is a relatively weak primary reinforcer, spurring research on other potential targets that may maintain smoking, including the potential benefits of nicotine on attention, inhibition, and reinforcer efficacy. The present study employs the most prevalent rodent model of ADHD, the spontaneously hypertensive rat (SHR) and its control comparison Wistar Kyoto (WKY) to examine the effects of acute and chronic subcutaneous nicotine injections on performance in three operant response inhibition paradigms. Functional activation in select regions of the prefrontal cortex and striatum was also explored. Acute (0.1, 0.3, 0.6 mg/kg) and chronic (0.3 mg/kg) nicotine increased impulsive responding regardless of strain, dose, or operant schedule. Dose-dependent decreases in latency to initiate the task were also observed. SHR receiving daily nicotine injections showed less activation in the nucleus accumbens shell compared to saline controls. Despite close similarities, one of the three operant tasks did not detect response inhibition deficits in SHR relative to WKY. A closer examination of these tasks may highlight critical components involved in the amelioration of response inhibition deficits.
ContributorsMazur, Gabriel Joseph (Author) / Sanabria, Federico (Thesis advisor) / Killeen, Peter R (Committee member) / Neisewander, Janet L (Committee member) / Wynne, Clive DL (Committee member) / Arizona State University (Publisher)
Created2014
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Description
The failure to withhold inappropriate behavior is a central component of most impulse control disorders, including Attention Deficit Hyperactivity Disorder (ADHD). The present study examined the effects of housing environment and methylphenidate (a drug often prescribed for ADHD) on the performance of rats in two response inhibition tasks: differential reinforcement

The failure to withhold inappropriate behavior is a central component of most impulse control disorders, including Attention Deficit Hyperactivity Disorder (ADHD). The present study examined the effects of housing environment and methylphenidate (a drug often prescribed for ADHD) on the performance of rats in two response inhibition tasks: differential reinforcement of low rate (DRL) and fixed minimum interval (FMI). Both tasks required rats to wait a fixed amount of time (6 s) before emitting a reinforced response. The capacity to withhold the target response (volitional inhibition) and timing precision were estimated on the basis of performance in each of the tasks. Paradoxically, rats housed in a mildly enriched environment that included a conspecific displayed less volitional inhibition in both tasks compared to rats housed in an isolated environment. Enriched housing, however, increased timing precision. Acute administration of methylphenidate partially reversed the effects of enriched housing. Implications of these results in the assessment and treatment of ADHD-related impulsivity are discussed.
ContributorsHill, Jade C (Author) / Sanabria, Federico (Thesis advisor) / Killeen, Peter (Committee member) / Neisewander, Janet (Committee member) / Arizona State University (Publisher)
Created2011
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Description
The purpose of this study, originally, was to contribute to the completion of a meta-analysis conducted by Mara Wierstra from the University of Virginia. Wierstra had requested individual participant data from two separate studies conducted in our lab: "Acute bouts of assisted cycling improves cognitive and upper extremity movement functions

The purpose of this study, originally, was to contribute to the completion of a meta-analysis conducted by Mara Wierstra from the University of Virginia. Wierstra had requested individual participant data from two separate studies conducted in our lab: "Acute bouts of assisted cycling improves cognitive and upper extremity movement functions in adolescents with Down syndrome" and "Assisted Cycling Therapy (ACT) improves inhibition in adolescents with autism spectrum disorder." From the data requested, the participants were required to complete three separate tests (i.e., Tower of London, Trail Making Task and the Stroop Test). After compiling the data and sending it to her, we decided to conduct a small meta-analysis of our own, drawing connecting conclusions from the data from the two studies. We concluded that observationally our data suggest an advantage for ACT over voluntary cycling and no cycling across two separate populations (i.e., Autism Spectrum Disorder and Down syndrome), and across different measures of executive function (i.e., Stroop Test, Trail Making Test, and Tower of London). The data suggest that the ACT interventions may promote the upregulation of neurotropic factors leading to neurogenesis in the prefrontal cortex of the brain.
ContributorsParker, Cade Joseph (Author) / Ringenbach, Shannon (Thesis director) / Holzapfel, Simon (Committee member) / School of Nutrition and Health Promotion (Contributor) / Barrett, The Honors College (Contributor)
Created2016-12
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Description
Temporal-order judgments can require integration of self-generated action-events and external sensory information. In a previous study, it was found that participants are biased to perceive one’s own action-events to occur prior to simultaneous external events. This phenomenon, named the “Egocentric Temporal Order Bias”, or ETO bias, was demonstrated as a

Temporal-order judgments can require integration of self-generated action-events and external sensory information. In a previous study, it was found that participants are biased to perceive one’s own action-events to occur prior to simultaneous external events. This phenomenon, named the “Egocentric Temporal Order Bias”, or ETO bias, was demonstrated as a 67% probability for participants to report self-generated events as occurring prior to simultaneous externally-determined events. These results were interpreted as supporting a feed-forward, constructive model of perception. However, the empirical data could support many potential mechanisms. The present study tests whether the ETO bias is driven by attentional differences, feed-forward predictability, or action. These findings support that participants exhibit a bias due to both feed-forward predictability and action, and a Bayesian analysis supports that these effects are quantitatively unique. Therefore, the results indicate that the ETO bias is largely driven by one’s own action, over and above feed-forward predictability.
ContributorsTang, Tim (Author) / Mcbeath, Michael K (Thesis advisor) / Brewer, Gene A. (Committee member) / Sanabria, Federico (Committee member) / Arizona State University (Publisher)
Created2020
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Description
Capacity limits of the human nervous system require important or rewarding information to be prioritized and encoded over less important or rewarding information. The present dissertation aims to identify structural and functional neural correlates of reward-motivated memory encoding. Chapter 1 reviews studies of reward-motivated memory encoding and their neural correlates,

Capacity limits of the human nervous system require important or rewarding information to be prioritized and encoded over less important or rewarding information. The present dissertation aims to identify structural and functional neural correlates of reward-motivated memory encoding. Chapter 1 reviews studies of reward-motivated memory encoding and their neural correlates, as well as the structure and function of dopaminergic midbrain circuits. Chapter 2 presents a study that utilizes electroencephalography (EEG) to determine which of two hypothesized processes underly the influence of reward value on episodic memory. One hypothesis is that value engages prefrontal executive control processes, so that valuable stimuli engage an elaborative rehearsal strategy that benefits memory. A second hypothesis is that value acts through the reward-related midbrain dopamine system to modulate synaptic plasticity in hippocampal and cortical efferents, thereby benefiting memory encoding. The results revealed that EEG signals thought to index dopamine-driven attention allocation were modulated by reward value and were positively correlated with individual differences in behavioral measures of memory prioritization. Chapter 3 employs diffusion-weighted magnetic resonance imaging (MRI) to dissociate heterogenous functional circuits of the midbrain reward system. The results comport with primate histology and show that midbrain circuits are differentially predictive of impulsivity and of attention-deficit hyperactivity disorder (ADHD). Chapter 4 presents a study that also employs diffusion-weighted MRI. The findings replicate Chapter 3 in dissociating heterogenous functional circuits of the midbrain reward system. Additionally, the structural integrity of midbrain-hippocampus circuits was quantified. Structural integrity of these circuits was positively correlated to behavioral measures of memory prioritization. These findings suggest that structural and functional measures of the dopaminergic reward system may underlie reward-motivated memory encoding in humans.
ContributorsElliott, Blake Louis (Author) / Brewer, Gene A (Thesis advisor) / McClure, Samuel M (Committee member) / Sanabria, Federico (Committee member) / Bae, Gi-Yeul (Committee member) / Arizona State University (Publisher)
Created2021