5,361 research outputs found

    STR-934: FATIGUE RESPONSE OF UHPC AS A CLOSURE STRIP MATERIAL IN PREFABRICATED BRIDGE APPLICATIONS

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    Replacement of concrete bridge decks can be an expensive process. In order to decrease costs and time of construction, precast deck panels can be used with closure strips cast in place between the panels. In order to ensure that these connections can withstand the rigors of a bridge’s life cycle, fatigue testing was completed on a specimen consisting of two precast concrete panels reinforced with GFRP and connected using a UHPC closure strip. These panels were subjected to 2,000,000 cycles of fatigue loading at three locations and subject to static failure loading at one location following fatigue loads. It was found that under fatigue loading the panels were able to maintain structural integrity while deflection values increased linearly following the initial cracking phase. At ultimate load, the panel failed in punching shear at levels less than those specified by bridge code. This is primarily due to the failure location adjacent to the closure strip failing on three punching shear planes and one plane along the interface between the UHPC

    The niche construction perspective: a critical appraisal

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    Niche construction refers to the activities of organisms that bring about changes in their environments, many of which are evolutionarily and ecologically consequential. Advocates of niche construction theory (NCT) believe that standard evolutionary theory fails to recognize the full importance of niche construction, and consequently propose a novel view of evolution, in which niche construction and its legacy over time (ecological inheritance) are described as evolutionary processes, equivalent in importance to natural selection. Here, we subject NCT to critical evaluation, in the form of a collaboration between one prominent advocate of NCT, and a team of skeptics. We discuss whether niche construction is an evolutionary process, whether NCT obscures or clarifies how natural selection leads to organismal adaptation, and whether niche construction and natural selection are of equivalent explanatory importance.We also consider whether the literature that promotes NCT overstates the significance of niche construction, whether it is internally coherent, and whether it accurately portrays standard evolutionary theory. Our disagreements reflect a wider dispute within evolutionary theory over whether the neo-Darwinian synthesis is in need of reformulation, as well as different usages of some key terms (e.g., evolutionary process)

    STR-923: FATIGUE OF STUD SHEAR CONNECTORS IN STEEL-PRECAST COMPOSITE BRIDGES

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    Modular bridge systems consisting of precast concrete deck panels connected to steel girders are becoming increasingly popular due to their rapid construction and optimal material utilization. The shear connection is a critical element of the system, having significant impacts on construction time, economic and environmental cost, structural integrity, and durability. Today welded shear studs are by far the most common type of shear connection. In steel-precast composite bridges, the studs are commonly grouped together so that the precast deck panels can be affixed to the girders by providing full depth “shear pockets” filled with grout. A laboratory beam testing program is underway at the University of Waterloo to investigate the effect of cyclic loading on stud shear connectors in cast-in-place and precast bridge girders. The program consists of twelve beam specimens, uniquely tested using a variable amplitude load history simulating Canadian highway truck traffic. In addition to yielding valuable S-N (stress plotted vs. the number of cycles until fatigue failure) data, initial test results provide evidence of the benefits of redundancy in the structural system and the value of beam tests over push-out tests. Calculating connector stresses in a composite beam is made complicated by interfacial slip and neutral axis migration. The end goal of this research is to provide Canadian bridge designers and erectors with improved design and construction recommendations in order to improve the efficiency and economy of this structural system for rapid bridge replacement projects

    Evolutionary theory and the ultimate-proximate distinction in the human behavioral sciences

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    To properly understand behavior, we must obtain both ultimate and proximate explanations. Put briefly, ultimate explanations are concerned with why a behavior exists, and proximate explanations are concerned with how it works. These two types of explanation are complementary and the distinction is critical to evolutionary explanation. We are concerned that they have become conflated in some areas of the evolutionary literature on human behavior. This article brings attention to these issues. We focus on three specific areas: the evolution of cooperation, transmitted culture, and epigenetics. We do this to avoid confusion and wasted effort—dangers that are particularly acute in interdisciplinary research. Throughout this article, we suggest ways in which misunderstanding may be avoided in the future

    Cisplatin Decreases Voluntary Wheel-Running Activity but Does Not Impair Food-Motivated Behavior in Mice

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    Cisplatin is a chemotherapeutic agent that is still commonly used to treat solid tumors. However, it has several toxic side effects due in large part to the mitochondrial damage that it induces. As this mitochondrial damage is likely to result in a decrease in the amount of metabolic energy that is available for behavioral activities, it is not surprising that fatigue develops in cancer patients treated with cisplatin. The present preclinical study was initiated to determine whether the detrimental effects of cisplatin were more pronounced on physical effort requiring a lot of energy versus effort that not only requires less energy but also procures energy in the form of food. For this purpose, mice were either trained to run in a wheel or to work for food in various schedules of food reinforcement before being treated with cisplatin. The experiments were carried out only in male mice as we had already reported that sex differences in cisplatin-induced neurotoxicities are minimal. Cisplatin was administered daily for one cycle of five days, or two cycles separated by a five-day rest. As observed in previous experiments, cisplatin drastically reduced voluntary wheel running. In contrast, when cisplatin was administered to food-restricted mice trained to work for a food reward in a progressive ratio schedule or in a fixed-interval schedule, it tended to increase the number of responses emitted to obtain the food rewards. This increase was not associated with any change in the temporal distribution of responses during the interval between two reinforcements in mice submitted to the fixed interval schedule of food reinforcement. When cisplatin was administered to food-restricted mice trained in an effort-based decision-making task in which they had to choose between working for a grain pellet with little effort and working for a preferred chocolate pellet with more effort, it decreased the total number of responses emitted to obtain food rewards. However, this effect was much less marked than the decrease in wheel running induced by cisplatin. The decrease in the effort invested in the procurement of food rewards was not associated with any change in the relative distribution of effort between low reward and high reward during the time course of the test session. These findings show that cisplatin decreases energy-consuming activities but not energy-procuring activities unless they require a choice between options differing in their cost-benefit ratio. Furthermore, they indicate that the physical dimension of fatigue is more likely to develop in cisplatin-treated individuals than the motivational dimension of fatigue

    Brief for the United States as Amicus Curiae in Support of Neither Party

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    Amicus ("friend of the court") brief written by the United States in support of neither party in AMP v. Myriad Genetics (No. 2010-1406)

    Lunar hand tools

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    Tools useful for operations and maintenance tasks on the lunar surface were determined and designed. Primary constraints are the lunar environment, the astronaut's space suit and the strength limits of the astronaut on the moon. A multipurpose rotary motion tool and a collapsible tool carrier were designed. For the rotary tool, a brushless motor and controls were specified, a material for the housing was chosen, bearings and lubrication were recommended and a planetary reduction gear attachment was designed. The tool carrier was designed primarily for ease of access to the tools and fasteners. A material was selected and structural analysis was performed on the carrier. Recommendations were made about the limitations of human performance and about possible attachments to the torque driver

    A phase Ib/II study of cabozantinib (XL184) with or without erlotinib in patients with non-small cell lung cancer.

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    PurposeCabozantinib is a multi-kinase inhibitor that targets MET, AXL, and VEGFR2, and may synergize with EGFR inhibition in NSCLC. Cabozantinib was assessed alone or in combination with erlotinib in patients with progressive NSCLC and EGFR mutations who had previously received erlotinib.MethodsThis was a phase Ib/II study (NCT00596648). The primary objectives of phase I were to assess the safety, pharmacokinetics, and pharmacodynamics and to determine maximum tolerated dose (MTD) of cabozantinib plus erlotinib in patients who failed prior erlotinib treatment. In phase II, patients with prior response or stable disease with erlotinib who progressed were randomized to single-agent cabozantinib 100 mg qd vs cabozantinib 100 mg qd and erlotinib 50 mg qd (phase I MTD), with a primary objective of estimating objective response rate (ORR).ResultsSixty-four patients were treated in phase I. Doses of 100 mg cabozantinib plus 50 mg erlotinib, or 40 mg cabozantinib plus 150 mg erlotinib were determined to be MTDs. Diarrhea was the most frequent dose-limiting toxicity and the most frequent AE (87.5% of patients). The ORR for phase I was 8.2% (90% CI 3.3-16.5). In phase II, one patient in the cabozantinib arm (N = 15) experienced a partial response, for an ORR of 6.7% (90% CI 0.3-27.9), with no responses for cabozantinib plus erlotinib (N = 13). There was no evidence that co-administration of cabozantinib markedly altered erlotinib pharmacokinetics or vice versa.ConclusionsDespite responses with cabozantinib/erlotinib in phase I, there were no responses in the combination arm of phase II in patients with acquired resistance to erlotinib. Cabozantinib did not appear to re-sensitize these patients to erlotinib
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