919 research outputs found

    Concentration of Manganese Dioxide from Philipsburg, Montana

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    Imports of manganese ore probably supply a major proportion of the needs of the United States. Domestic production is reported to be higher than pre-war levels, but does not equal that of the peak production year of 1943. In 1946, the Anaconda Copper Mining Company acĀ­counted for 90 percent of the total shipments of manganĀ­ese nodules, and this company is the largest producer of domestic metallurgical ore in the United States

    Social Influences on Inequity Aversion in Children

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    Adults and children are willing to sacrifice personal gain to avoid both disadvantageous and advantageous inequity. These two forms of inequity aversion follow different developmental trajectories, with disadvantageous inequity aversion emerging around 4 years and advantageous inequity aversion emerging around 8 years. Although inequity aversion is assumed to be specific to situations where resources are distributed among individuals, the role of social context has not been tested in children. Here, we investigated the influence of two aspects of social context on inequity aversion in 4- to 9-year-old children: (1) the role of the experimenter distributing rewards and (2) the presence of a peer with whom rewards could be shared. Experiment 1 showed that children rejected inequity at the same rate, regardless of whether the experimenter had control over reward allocations. This indicates that childrenā€™s decisions are based upon reward allocations between themselves and a peer and are not attempts to elicit more favorable distributions from the experimenter. Experiment 2 compared rejections of unequal reward allocations in children interacting with or without a peer partner. When faced with a disadvantageous distribution, children frequently rejected a smaller reward when a larger reward was visible, even if no partner would obtain the larger reward. This suggests that nonsocial factors partly explain disadvantageous inequity rejections. However, rejections of disadvantageous distributions were higher when the larger amount would go to a peer, indicating that social context enhances disadvantageous inequity aversion. By contrast, children rejected advantageous distributions almost exclusively in the social context. Therefore, advantageous inequity aversion appears to be genuinely social, highlighting its potential relevance for the development of fairness concerns. By comparing social and nonsocial factors, this study provides a detailed picture of the expression of inequity aversion in human ontogeny and raises questions about the function and evolution of inequity aversion in humans

    Placebo Bait Uptake Trial to Test Feasibility of Polynesian Rat (\u3ci\u3eRattus exulans\u3c/i\u3e) Eradication on Wake Atoll

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    Rodent eradications have contributed to the recovery of many threatened species, but challenges often exist for campaigns that occur on tropical islands when compared to more temperate regions. A post-operational review of a rat eradication operation on Wake Atoll indicated that certain areas, such as those with high alternative food abundance, may have contributed to the failure to remove all Polynesian rats. We conducted a nontoxic bait uptake trial to evaluate whether the maximum prescribed bait application rate for Brodifacoum-25W rodenticide pellets was sufficient to expose all rats to a lethal dose at three sites on Wake Atoll, including around a solid waste aggregation area (SWAA), which was previously identified as ā€œhigh risk.ā€ We monitored bait persistence and condition throughout the treatment period as well as rat movement via radio tracking. Bait uptake by rats was also assessed by trapping and examination of rat orifices and gastrointestinal contents for pyranine biomarker incorporated into the bait pellets. The rate of bait disappearance differed by site, with bait disappearing the fastest in vicinity of the SWAA. Rat movement also varied by site, with rats observed traveling greater distances around the SWAA, sometimes exceeding 300 m. The SWAA was the only site at which we observed rats negative for biomarker exposure. We suggest that these negative observations resulted from lack of bait availability or movement of rats into the core trapping area from outside the treatment area. However, we cannot rule out preferential selection of alternative food sources over bait pellets and suggest that this possibility should receive further attention. Based on our results, we conclude that, of the three sites, the maximum bait application rate prescribed on the product label was not high enough to provide every rat an opportunity to encounter bait at and around the SWAA. Given the rapid disappearance of bait and the regular immigration of rats from distant habitat, we recommend that an even greater application rate be prescribed and that the heavier treatment be extended over a much larger area surrounding the SWAA

    The mechanism of twin thickening and the elastic strain state of TWIP steel nanotwins

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    A Twinning Induced Plasticity (TWIP) steel with a nominal composition of Fe-16.4Mn-0.9C-0.5Si-0.05Nb-0.05V was deformed to an engineering strain of 6\%. The strain around the deformation twins were mapped using the 4D-STEM technique. Strain mapping showed a large average elastic strain of approximately 6\% in the directions parallel and perpendicular to the twinning direction. However, the large average strain comprised of several hot spots of even larger strains of up to 12\%. These hot spots could be attributed to a high density of sessile Frank dislocations on the twin boundary and correspond to shear stresses of 1--1.5 GPa. The strain and therefore stress fields are significantly larger than other materials known to twin and are speculated to be responsible for the early thickness saturation of TWIP steel nanotwins. The ability to keep twins extremely thin helps improve grain fragmentation, \textit{i.e.} the dynamic Hall-Petch effect, and underpins the large elongations and strain hardening rates in TWIP steels

    Social representations of HIV/AIDS in five Central European and Eastern European countries: A multidimensional analysis

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    Cognitive processing models of risky sexual behaviour have proliferated in the two decades since the first reporting of HIV/AIDS, but far less attention has been paid to individual and group representations of the epidemic and the relationship between these representations and reported sexual behaviours. In this study, 494 business people and medics from Estonia, Georgia, Hungary, Poland and Russia sorted free associations around HIV/AIDS in a matrix completion task. Exploratory factor and multidimensional scaling analyses revealed two main dimensions (labelled ā€˜Sexā€™ and ā€˜Deadly diseaseā€™), with significant cultural and gender variations along both dimension scores. Possible explanations for these results are discussed in the light of growing concerns over the spread of the epidemic in this region

    Poliomyelitis in Intraspinally Inoculated Poliovirus Receptor Transgenic Mice

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    AbstractMice transgenic with the human poliovirus receptor gene develop clinical signs and neuropathology similar to those of human poliomyelitis when neurovirulent polioviruses are inoculated into the central nervous system (CNS). Factors contributing to disease severity and the frequencies of paralysis and mortality include the poliovirus strain, dose, and gender of the mouse inoculated. The more neurovirulent the virus, as defined by monkey challenge results, the higher the rate of paralysis, mortality, and severity of disease. Also, the time to disease onset is shorter for more neurovirulent viruses. Male mice are more susceptible to polioviruses than females. TGM-PRG-3 mice have a 10-fold higher transgene copy number and produce 3-fold more receptor RNA and protein levels in the CNS than TGM-PRG-1 mice. CNS inoculations with type III polioviruses differing in relative neurovirulence show that these mouse lines are similar in disease frequency and severity, demonstrating that differences in receptor gene dosage and concomitant receptor abundance do not affect susceptibility to infection. However, there is a difference in the rate of accumulation of clinical signs. The time to onset of disease is shorter for TGM-PRG-3 than TGM-PRG-1 mice. Thus, receptor dosage affects the rate of appearance of poliomyelitis in these mice
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