Graduation date: 1971

Thesis (M.S.)--Oregon Graduate Center, 1980.

Thesis (Ph. D.)--Oregon Graduate Center, 1979.

Twenty-four crossbred steer calves (235 + 6 kg initial BW) were weaned, adapted to a growing diet, trained to use Calan feeders and assigned to one of four treatments in a 2 x 2 factorial arrangement as follows: (1) no transit stress and saline injection, (2) no transit stress and trace mineral and vitamin E (TM/VitE) injections, (3) transit stress and saline injection and (4) transit stress and TM/VitE injection. TM/VitE injections consisted of MultiminTM to provide 0.3, 0.6, 0.15 and 0.6 mg of Cu, Mn, Se, and Zn/kg BW, respectively, and Vita ETM to provide 9 IU of VitE/kg BW on d 0 and 21 of the study. On d 24, transit-stressed steers were subjected to a three-d, 2000-km, transportation period. During the 56-d experiment, liver and serum samples were assayed to assess trace mineral status, antibody titers to keyhole limpet hemocyanin (KLH) measured to assess humoral immunity and phytohemagglutinin(PHA)- and ovalbumin(OVA)-induced skin swelling and lymphocyte proliferation measured to assess cellular immunity. TM/VitE-injected steers grew slower (P < 0.05) over the first 24 d of the experiment and tended (P = 0.10) to grow slower after transit. TM/VitE injections increased (P < 0.05) liver Cu and Zn concentrations 135 and 21 % by d 30, respectively. TM/VitE-injected steers had increased (P < 0.05) serum Cu on d 24 and 26, but decreased (P < 0.05) serum Zn and whole blood Se compared to saline-injected steers on d 24 and 56. TM/VitE injections increased serum α-tocopherol concentrations. TM/VitE injections did not affect humoral immunity, but decreased (P < 0.05) skin-swelling responses to PHA on d 21, and decreased (P < 0.05) lymphocyte proliferation to OVA and KLH. Transit-stressed steers had higher (P < 0.05) serum Cu on d 26, and higher (P < 0.05) liver Cu concentrations on d 56 than non-transit-stressed steers. Transit stress did not affect serum Zn or whole blood Se concentrations. Injections of TM/VitE increased Cu, Zn and vitamin E, but not Se status. The TM/VitE treatment suppressed growth and cellular immune function suggesting that levels of trace minerals used in this study were too high.

This thesis represents a culmination of work which seeks to examine the prelimbic and anterior cingulate cortex (ACC) during trace fear memory across sleep and wakefulness states. In order to accomplish this task, a technical platform needed to be developed. Accordingly, the first chapter demonstrates that fear behavior can recorded utilizing neck electromyography (EMG). The second chapter examines the role of the ACC in trace fear memory, discovering that many neurons have premotor activity related to freezing behavior. Additionally, auditory-evoked potentials in the ACC demonstrate learning curves which match learning curves of fear. We suggest that the ACC is involved in affective-motor integration. The third chapter examines how genetic enhancement of trace fear learning, with calcium/calmodulin-dependent protein kinase IV (CaMKIV) over-expressed mice, can influence electro-cortical potentials during wakefulness, learning and sleep. We found that CaMKIV potentiates electro-cortical brain waves during learning and sleep. In particular 4-7.5Hz rhythms were potentiated in CaMKIV over-expressed mice during learning, and are likely to be localized to regions of the prelimbic cortex. Taken together the results of this thesis demonstrate that the trace fear memory paradigm engages the ACC and prelimbic regions, as evidenced at the single cell and cortical field potential level, for sensory-affective and premotor functions related to anticipating painful stimulation. CaMKIV appears to be a protein which modulates learning and electro-cortical potentials and may be a potential target for sleep-dependent memory consolidation in the prefrontal cortex.

This thesis represents a culmination of work which seeks to examine the prelimbic and anterior cingulate cortex (ACC) during trace fear memory across sleep and wakefulness states. In order to accomplish this task, a technical platform needed to be developed. Accordingly, the first chapter demonstrates that fear behavior can recorded utilizing neck electromyography (EMG). The second chapter examines the role of the ACC in trace fear memory, discovering that many neurons have premotor activity related to freezing behavior. Additionally, auditory-evoked potentials in the ACC demonstrate learning curves which match learning curves of fear. We suggest that the ACC is involved in affective-motor integration. The third chapter examines how genetic enhancement of trace fear learning, with calcium/calmodulin-dependent protein kinase IV (CaMKIV) over-expressed mice, can influence electro-cortical potentials during wakefulness, learning and sleep. We found that CaMKIV potentiates electro-cortical brain waves during learning and sleep. In particular 4-7.5Hz rhythms were potentiated in CaMKIV over-expressed mice during learning, and are likely to be localized to regions of the prelimbic cortex. Taken together the results of this thesis demonstrate that the trace fear memory paradigm engages the ACC and prelimbic regions, as evidenced at the single cell and cortical field potential level, for sensory-affective and premotor functions related to anticipating painful stimulation. CaMKIV appears to be a protein which modulates learning and electro-cortical potentials and may be a potential target for sleep-dependent memory consolidation in the prefrontal cortex.

There is a widespread use of thermal hydraulic codes in nuclear industry. The codesare used to analyse the transient and steady-state behavior of the nuclear powerplants. The US Nuclear Regulatory Commission that has long experience of developing such codes are now incorporating the capabilities of their earlier codes into one modern simulation tool, called TRACE. The code is under development and validation work is required especially in the field of BWR applications. Eventually the code is expected to replace similar codes such as TRAC and Relap5. With this in mind, a TRACE model of Forsmark 1 has been set up to investigate how well it can simulate a plant transient. On the 25th of July, 2006 there was a disturbance at Forsmark 1 that caused the RPV water level and pressure to decrease.In this project, plant data acquired during the event are used to validate the model of Forsmark 1. The validation work is focused on comparing measured and calculated water and pressure levels in the RPC during the transient. The results show qualitatively good agreement with the validation data, however during a period of the simulations there are large discrepancies concerning the pressure and water level in the RPV. In total, 13 simulations are performed, studying the influences of parameters such as simulation time-step size, the feed water flow boundary conditions and the steam line isolation valve characteristics. Based on the results of the simulations, a number of recommendations are made regarding suggestions for further work.

Tracing represents that the information which are generated from the system can be collected for later observation and analysis. Because the SoC design becomes more and more complex, an advanced tracing is needed instead of processor tracing only. However, the generation rate and the size of real time system traces are so huge such that the compressor for tracing is needed. In this thesis, we purpose an on-chip bus trace analyzer for SoC¡¦s. This trace analyzer can allowed to perform accurate, successive trace collection in an unlimited time and can be used in various embedded system without influencing the operation of the bus system. The approach consists of two stages: (1) timing/signal abstraction stage and (2) trace reducing stage. And we show how to design and implement the on-chip bus trace analyzer. It can be also configured by users for different debugging uses. The experimental results show that this bus trace analyzer can reach a good compression ratio of 99% for AMBA system. Hence, by utilizing this trace analyzer, the support for debugging can be more powerful than existing method.

Twenty-four crossbred steer calves (235 + 6 kg initial BW) were weaned, adapted to a growing diet, trained to use Calan feeders and assigned to one of four treatments in a 2 x 2 factorial arrangement as follows: (1) no transit stress and saline injection, (2) no transit stress and trace mineral and vitamin E (TM/VitE) injections, (3) transit stress and saline injection and (4) transit stress and TM/VitE injection. TM/VitE injections consisted of MultiminTM to provide 0.3, 0.6, 0.15 and 0.6 mg of Cu, Mn, Se, and Zn/kg BW, respectively, and Vita ETM to provide 9 IU of VitE/kg BW on d 0 and 21 of the study. On d 24, transit-stressed steers were subjected to a three-d, 2000-km, transportation period. During the 56-d experiment, liver and serum samples were assayed to assess trace mineral status, antibody titers to keyhole limpet hemocyanin (KLH) measured to assess humoral immunity and phytohemagglutinin(PHA)- and ovalbumin(OVA)-induced skin swelling and lymphocyte proliferation measured to assess cellular immunity. TM/VitE-injected steers grew slower (P < 0.05) over the first 24 d of the experiment and tended (P = 0.10) to grow slower after transit. TM/VitE injections increased (P < 0.05) liver Cu and Zn concentrations 135 and 21 % by d 30, respectively. TM/VitE-injected steers had increased (P < 0.05) serum Cu on d 24 and 26, but decreased (P < 0.05) serum Zn and whole blood Se compared to saline-injected steers on d 24 and 56. TM/VitE injections increased serum &#945;-tocopherol concentrations. TM/VitE injections did not affect humoral immunity, but decreased (P < 0.05) skin-swelling responses to PHA on d 21, and decreased (P < 0.05) lymphocyte proliferation to OVA and KLH. Transit-stressed steers had higher (P < 0.05) serum Cu on d 26, and higher (P < 0.05) liver Cu concentrations on d 56 than non-transit-stressed steers. Transit stress did not affect serum Zn or whole blood Se concentrations. Injections of TM/VitE increased Cu, Zn and vitamin E, but not Se status. The TM/VitE treatment suppressed growth and cellular immune function suggesting that levels of trace minerals used in this study were too high.

In the System on a Chip () era, more components are embedded in one chip. Therefore, it has been an important issue to assist verification and debugging by observing the signals inside of a chip. The bus signals tracing is a general method to resolve it. However, the quantities of signals that have to be traced in an are very huge, we must to reduce the trace data as more as possible. Because of the reasons described as above, we propose a hardware called multi-resolution bus tracer to overcome these problems in this thesis. In the bus tracer, user can changes the observed accuracy of tracing signals dynamically during the program execution, and reduces all those signals efficiently. The experiment results show that bus tracer can achieve 85% average compressed ratio on the forward tracing, and 84% average compressed ratio on the backward tracing. In the other hand, the software called trace data analyzer not only transfers the trace signals into Value Change Dump (VCD) file format but also provides some essential analyses for user observation. Finally, our IP (Intelligent Property) has been integrated into a real platform: 3D Graphics Acceleration, and tape-out successfully. Therefore, using the multi-resolution bus trace analyzer can promote the abilities of system debugging efficiently.