2,050 research outputs found
Computer simulation of the primary recoil spectra and damage cross section of Fe₃Al using ENDF/B II data
A computer program, using Evaluated Nuclear Data File (ENDF/B II) information, was used to develop energy-exchange kernels which delineate the energy transfer probabilities between neutrons and Fe3Al lattice atoms. The kernels combine all available information on elastic and inelastic scattering contained in the ENDF/B II data.
The computer program used to generate the primary recoil spectra is SAKI, a modified version of RICE (1). SAKI is designed to calculate energy-exchange probabilities in any binary alloy as well as damage cross sections and optimum cutoff energies for use in comparing displacement effects in different reactor spectra. --Abstract, page ii
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The price tag of regulated open access for for-hire recreational fisheries
Saltwater recreational fisheries receive little attention compared to their commercial counterparts. Yet recreational fisheries can suffer from many of the same symptoms of open access as commercial fisheries. Regulations designed to allocate a scarce supply, such as seasonal closures augmented with bag and size limits, can result in significant losses of welfare to anglers. We provide an estimate of these foregone benefits by estimating the potential gains to implementing rights-based reforms of the headboat portion of the recreational red snapper fishery in the US Gulf of Mexico (GOM) – a fishery which has suffered from a regulatory spiral of shortened seasons and lowered bag limits in spite of rebuilding stocks. We gather primary survey data of headboat anglers that elicits their planned number and seasonal distribution of trips under status-quo management and alternative arrangements with year-round retention of red snapper and compensating increases in prices or lowered bag limits. We utilize these data to estimate a Kuhn-Tucker demand model of anglers’ seasonal demand for trips as a function of the ability to retain red snapper and bag limits and prices. We find that a hypothetical rights-based policy under which vessels could offer their customers year-round fishing, in exchange for lower per-angler retention and increased prices, could raise individual headboat anglers' welfare by an average of $139/year. These estimates, when placed in the context of the overall scope of recreational fishing around the world, suggests that status-quo management of scarce fish stocks may cost anglers billions of dollars a year
Reproductive inequality in humans and other mammals
To address claims of human exceptionalism, we determine where humans fit within the greater mammalian distribution of reproductive inequality. We show that humans exhibit lower reproductive skew (i.e., inequality in the number of surviving offspring) among males and smaller sex differences in reproductive skew than most other mammals, while nevertheless falling within the mammalian range. Additionally, female reproductive skew is higher in polygynous human populations than in polygynous nonhumans mammals on average. This patterning of skew can be attributed in part to the prevalence of monogamy in humans compared to the predominance of polygyny in nonhuman mammals, to the limited degree of polygyny in the human societies that practice it, and to the importance of unequally held rival resources to women’s fitness. The muted reproductive inequality observed in humans appears to be linked to several unusual characteristics of our species—including high levels of cooperation among males, high dependence on unequally held rival resources, complementarities between maternal and paternal investment, as well as social and legal institutions that enforce monogamous norms
Reproductive inequality in humans and other mammals
To address claims of human exceptionalism, we determine where humans fit within the greater mammalian distribution of reproductive inequality. We show that humans exhibit lower reproductive skew (i.e., inequality in the number of surviving offspring) among males and smaller sex differences in reproductive skew than most other mammals, while nevertheless falling within the mammalian range. Additionally, female reproductive skew is higher in polygynous human populations than in polygynous nonhumans mammals on average. This patterning of skew can be attributed in part to the prevalence of monogamy in humans compared to the predominance of polygyny in nonhuman mammals, to the limited degree of polygyny in the human societies that practice it, and to the importance of unequally held rival resources to women's fitness. The muted reproductive inequality observed in humans appears to be linked to several unusual characteristics of our species-including high levels of cooperation among males, high dependence on unequally held rival resources, complementarities between maternal and paternal investment, as well as social and legal institutions that enforce monogamous norms
“Others-in-Law”: Legalism in the Economy of Religious Differences
Religious legalism encompasses a wide range of attitudes that assign religious meaning to legal content or to legal compliance. The phenomenology of religious legalism is assuming a significant role in various contemporary debates about legal pluralism, accommodation of religious minorities, religious freedom, and so forth. This article revises this conception and the commonplace equation of Judaism and legalism. It suggests that we ought to regard both as part of the economy of religious differences by which religious identities are expressed and defined as alternatives. The common ascription of religious legalism to Judaism (and Islam) is criticized here through a historical analysis of the law-religion-identity matrix in three cultural settings: late ancient Judeo-Hellenic, medieval Judeo–Arabic, and post-Reformation Europe
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
There is tremendous potential for genome sequencing to improve clinical diagnosis and care once it becomes routinely accessible, but this will require formalizing research methods into clinical best practices in the areas of sequence data generation, analysis, interpretation and reporting. The CLARITY Challenge was designed to spur convergence in methods for diagnosing genetic disease starting from clinical case history and genome sequencing data. DNA samples were obtained from three families with heritable genetic disorders and genomic sequence data were donated by sequencing platform vendors. The challenge was to analyze and interpret these data with the goals of identifying disease-causing variants and reporting the findings in a clinically useful format. Participating contestant groups were solicited broadly, and an independent panel of judges evaluated their performance.
RESULTS:
A total of 30 international groups were engaged. The entries reveal a general convergence of practices on most elements of the analysis and interpretation process. However, even given this commonality of approach, only two groups identified the consensus candidate variants in all disease cases, demonstrating a need for consistent fine-tuning of the generally accepted methods. There was greater diversity of the final clinical report content and in the patient consenting process, demonstrating that these areas require additional exploration and standardization.
CONCLUSIONS:
The CLARITY Challenge provides a comprehensive assessment of current practices for using genome sequencing to diagnose and report genetic diseases. There is remarkable convergence in bioinformatic techniques, but medical interpretation and reporting are areas that require further development by many groups
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