Extension of the Color Glass Condensate Approach to Diffractive Reactions

We present an evolution equation for the Bjorken x dependence of diffractive dissociation on hadrons and nuclei at high energies. We extend the formulation of Kovchegov and Levin by relaxing the factorization assumption used there. The formulation is based on a technique used by Weigert to describe interjet energy flow. The method can be naturally extended to other exclusive observables

On Orbital Period Changes in Nova Outbursts

We propose a new mechanism that produces an orbital period change during a nova outburst. When the ejected material carries away the specific angular momentum of the white dwarf, the orbital period increases. A magnetic field on the surface of the secondary star forces a fraction of the ejected material to corotate with the star, and hence the binary system. The ejected material thus takes angular momentum from the binary orbit and the orbital period decreases. We show that for sufficiently strong magnetic fields on the surface of the secondary star, the total change to the orbital period could even be negative during a nova outburst, contrary to previous expectations. Accurate determinations of pre- and post-outburst orbital periods of recurrent nova systems could test the new mechanism, in addition to providing meaningful constraints on otherwise difficult to measure physical quantities. We apply our mechanism to outbursts of the recurrent nova U Sco.Comment: Accepted for publication in MNRA

Respiratory influences on pupil size dynamics and visual recognition memory

Breathing, a fundamental rhythm of life, has traditionally been associated with the exchange of oxygen and carbon dioxide. However, recent research in both animal models and humans has unveiled additional roles of respiration in modulating cortical neuronal activity, influencing sensory, motor, emotional, and cognitive processes. This dissertation aims to explore the impact of respiration on pupil size dynamics and visual recognition memory in humans. In Study I, we synthesized the research conducted on respiratory influences on pupil size dynamics in humans by conducting a systematic literature review. We discovered that the evidence for respiratory influences on pupil size dynamics in humans is less solid and extensive than previously believed. After more than 50 years of research, only 12 studies have directly investigated this topic. Not only was the underlying evidence for an effect of breathing phase, depth, and rate on pupil size dynamics weak, but the influence of breathing route (oral or nasal breathing) had not been investigated at all. In Study II, we conducted an experimental study to answer the outstanding questions identified in Study I. We collected pupil size data from participants during periods of rest while they breathed through their nose and mouth, on separate occasions. We demonstrated small but significant effects of breathing phase on pupil size and a spurious correlation and phase synchronization between the breathing and the pupil signal that is largely driven by breathing rate. After accounting for this spurious correlation and phase synchronization, we show that a small but significant interaction between the breathing and the pupil signal remains. Importantly, we show that, contrary to common belief, pupil size does not increase during inhalation, but rather during exhalation. Furthermore, we did not find any changes in pupil size in the time around inhalation and exhalation, and our results were not affected by the breathing route. In conclusion, we confirmed the influence of breathing on pupil size dynamics, while uncovering a more complex and intricate relationship than previously conceived. In Study III, we investigated the influence of breathing phase and breathing route on performance in a visual recognition memory task with a within-subject design and with stimuli presentation phase-locked to the inhalation or exhalation onset. We show that neither breathing phase nor breathing route affect memory performance. However, we did find an effect of breathing phase on response bias, with participants using a more conservative response bias during exhalation. Furthermore, we found that breathing route and breathing phase shape the Late Parietal Effect (LPE), but not the Frontal Negative Component (FN400), amplitude during encoding. Additionally, during recognition, both the LPE and FN400 component amplitudes were not, or only to a small extent, affected by breathing route and phase. While we demonstrated that breathing does not shape visual recognition memory performance, we also showed that breathing influences brain activity related to memory functions. Therefore, we highlight the importance of further research to elucidate the extent of respiratory influence on perception, cognition, and behavior. In Study IV, we further investigated the impact of breathing on visual memory performance by investigating the effects of nasal breathing phase on memory of repeated images presented in a rapid serial visual presentation (RSVP) task. In two separate, high-powered experiments, we did not find an effect of breathing phase on task performance. An exploratory analysis in the first experiment discovered a potential performance increase for stimuli presented approximately one second after inhalation. However, this was not replicated in the second, larger, and pre-registered study. Thus, we find no effect of breathing phase on performance in this RSVP task and urge for caution regarding the notion that visual memory is broadly affected by the breathing phase. Finally, in Study V, we investigated whether oral hormonal contraceptives (OC) affect chemosensory sensitivity and perception. Whereas previous research focused nearly exclusively on olfaction, we expanded this to also study the taste and trigeminal sense. Making use of Bayesian statistics, we evaluated the performance differences between a group of women taking OC, and a control group of normal cycling women. Our results indicated that the use of OC does not affect odor, trigeminal, or taste detection thresholds. Furthermore, neither odor nor taste perception were affected, with Bayes factors weighing the evidence in favor of the null hypothesis. We therefore conclude it to be unlikely that OC affect chemosensory perception to a degree that is of behavioral relevance. Collectively, this doctoral thesis challenges prevailing myths while paving the way for a more intricate understanding of the relationship between respiration and pupil size, and perceptual and cognitive processes. Importantly, it underscores the importance of implementing rigorous methodological paradigms in future research

PLANNING AND COORDINATION IN DRIVING SIMULATION

We present an overview of coordination and planning tasks that we face with during the development of the AgentDrive simulation platform. We particularly describe an integration of the AgentDrive with a driving simulator OpenDS. We demonstrate how the planning and coordination mechanisms can be applied in a driving simulator for automated driving applications or realistic traffic generation. We emphasize particular planning and/or coordination methods that were already developed using AgentDrive platform

Are fruit colors adapted to consumer vision and birds equally efficient in detecting colorful signals?

Reproduction in plants often requires animal vectors. Fruit and flower colors are traditionally viewed as an adaptation to facilitate detection for pollinators and seed dispersers. This long-standing hypothesis predicts that fruits are easier to detect against their own leaves compared with those of different species. We tested this hypothesis by analyzing the chromatic contrasts between 130 bird-dispersed fruits and their respective backgrounds according to avian vision. From a bird's view, fruits are not more contrasting to their own background than to those of other plant species. Fruit colors are therefore not adapted toward maximized conspicuousness for avian seed dispersers. However, secondary structures associated with fruit displays increase their contrasts. We used fruit colors to assess whether the ultraviolet and violet types of avian visual systems are equally efficient in detecting color signals. In bright light, the chromatic contrasts between fruit and background are stronger for ultraviolet vision. This advantage is due to the lesser overlap in spectral sensitivities of the blue and ultraviolet cones, which disappears in dim light conditions. We suggest that passerines with ultraviolet cones might primarily use epigamic signals that are less conspicuous to their avian predators (presumably with violet vision). Possible examples for such signals are carotenoid-based signals