Naval Services Game \u2713

Conducted from 27-31 January 2014 at the United States Naval war College in Newport, Rhode Island, the Naval Services Game brought together 30 members of the Navy and Marine Corps for the Navy and Marine Corps for the purpose of exploring U.S. Navy and U.S. Marine Corps integration, The intent of this integration is to develop forward deployed naval forces with integrated capabilities for engagement and crisis responses. Participants were assigned to three, independent (Blue) player cells. These cells were tasked similarly with players providing a perspective of the service component commander in theater initially, then the Service Chief

Naval Services Game \u2712

The United States Naval War College (NWC) in Newport, Rhode Island, in partnership with the Marine Corps Warfighting Laboratory (MCWL), hosted the Naval Services Game (NSG) from 11-13 September 2012. The NSG was developed and executed under the sponsorship of the Naval Board. The purpose of the NSG was to explore the challenges associated with aggregating naval forces in response to an emerging conflict

Naval Services Game \u2713: Game Report

Conducted form 27-31 January 2014 in Newport, Rhode Island, and under the design, direction and analysis of the United States Naval War College (NWC) and the Marine Corps Warfighter Laboratory (MCWL), the Naval Services Game (NSG) brought together 30 members of the Navy and Marine Corps to explore U.S. Marine Corps integration. The intent of this exploration is to help develop forward deployed naval forces with integrated capabilities for engagement and crisis response

Magnets, magic, and other anomalies:In defense of methodological naturalism

Funding for this research was provided by the John Templeton Foundation, grant number 59023Recent critiques of methodological naturalism (MN) claim that it fails by conflicting with Christian belief and being insufficiently humble. We defend MN by tracing the real history of the debate, contending that the story as it is usually told is mythic. We show how MN works in practice, including among real scientists. The debate is a red herring. It only appears problematic because of confusion among its opponents about how scientists respond to experimental anomalies. We conclude by introducing our preferred approach, Science‐Engaged Theology.PostprintPeer reviewe

Probing the Black Hole Engine with Measurements of the Relativistic X-ray Reflection Component

Over the last decades X-ray spectroscopy has proven to be a powerful tool for the estimation of black hole spin and several other key parameters in dozens of AGN and black hole X-ray binaries. In this White Paper, we discuss the observational and theoretical challenges expected in the exploration, discovery, and study of astrophysical black holes in the next decade. We focus on the case of accreting black holes and their electromagnetic signatures, with particular emphasis on the measurement of the relativistic reflection component in their X-ray spectra.Comment: Astro 2020 Decadal science White Pape

BioDMET: a physiologically based pharmacokinetic simulation tool for assessing proposed solutions to complex biological problems

We developed a detailed, whole-body physiologically based pharmacokinetic (PBPK) modeling tool for calculating the distribution of pharmaceutical agents in the various tissues and organs of a human or animal as a function of time. Ordinary differential equations (ODEs) represent the circulation of body fluids through organs and tissues at the macroscopic level, and the biological transport mechanisms and biotransformations within cells and their organelles at the molecular scale. Each major organ in the body is modeled as composed of one or more tissues. Tissues are made up of cells and fluid spaces. The model accounts for the circulation of arterial and venous blood as well as lymph. Since its development was fueled by the need to accurately predict the pharmacokinetic properties of imaging agents, BioDMET is more complex than most PBPK models. The anatomical details of the model are important for the imaging simulation endpoints. Model complexity has also been crucial for quickly adapting the tool to different problems without the need to generate a new model for every problem. When simpler models are preferred, the non-critical compartments can be dynamically collapsed to reduce unnecessary complexity. BioDMET has been used for imaging feasibility calculations in oncology, neurology, cardiology, and diabetes. For this purpose, the time concentration data generated by the model is inputted into a physics-based image simulator to establish imageability criteria. These are then used to define agent and physiology property ranges required for successful imaging. BioDMET has lately been adapted to aid the development of antimicrobial therapeutics. Given a range of built-in features and its inherent flexibility to customization, the model can be used to study a variety of pharmacokinetic and pharmacodynamic problems such as the effects of inter-individual differences and disease-states on drug pharmacokinetics and pharmacodynamics, dosing optimization, and inter-species scaling. While developing a tool to aid imaging agent and drug development, we aimed at accelerating the acceptance and broad use of PBPK modeling by providing a free mechanistic PBPK software that is user friendly, easy to adapt to a wide range of problems even by non-programmers, provided with ready-to-use parameterized models and benchmarking data collected from the peer-reviewed literature

Orbital Decay in M82 X-2

© 2022. The Author(s). Published by the American Astronomical Society. This is an open access article distributed under the Creative Commons Attribution License, to view a copy of the license, https://creativecommons.org/licenses/by/4.0/M82 X-2 is the first pulsating ultraluminous X-ray source discovered. The luminosity of these extreme pulsars, if isotropic, implies an extreme mass transfer rate. An alternative is to assume a much lower mass transfer rate, but with an apparent luminosity boosted by geometrical beaming. Only an independent measurement of the mass transfer rate can help discriminate between these two scenarios. In this paper, we follow the orbit of the neutron star for 7 yr, measure the decay of the orbit ( Ṗorb/Porb≈−8·10−6yr−1 ), and argue that this orbital decay is driven by extreme mass transfer of more than 150 times the mass transfer limit set by the Eddington luminosity. If this is true, the mass available to the accretor is more than enough to justify its luminosity, with no need for beaming. This also strongly favors models where the accretor is a highly magnetized neutron star.Peer reviewe

X-UDS: The Chandra Legacy Survey of the UKIDSS Ultra Deep Survey Field

We present the X-UDS survey, a set of wide and deep Chandra observations of the Subaru-XMM Deep/UKIDSS Ultra Deep Survey (SXDS/UDS) field. The survey consists of 25 observations that cover a total area of 0.33 deg(2). The observations are combined to provide a nominal depth of similar to 600 ks in the central 100 arcmin(2) region of the field that has been imaged with Hubble/WFC3 by the CANDELS survey and similar to 200 ks in the remainder of the field. In this paper, we outline the survey's scientific goals, describe our observing strategy, and detail our data reduction and point source detection algorithms. Our analysis has resulted in a total of 868 band-merged point sources detected with a false-positive Poisson probability of <1 x 10(-4). In addition, we present the results of an X-ray spectral analysis and provide best-fitting neutral hydrogen column densities, N-H, as well as a sample of 51 Compton-thick active galactic nucleus candidates. Using this sample, we find the intrinsic Compton-thick fraction to be 30%-35% over a wide range in redshift (z = 0.1-3), suggesting the obscured fraction does not evolve very strongly with epoch. However, if we assume that the Compton-thick fraction is dependent on luminosity, as is seen for Compton-thin sources, then our results are consistent with a rise in the obscured fraction out to z similar to 3. Finally, an examination of the host morphologies of our Compton-thick candidates shows a high fraction of morphological disturbances, in agreement with our previous results. All data products described in this paper are made available via a public website

Development of the lateral ventricular choroid plexus in a marsupial, Monodelphis domestica

<p>Abstract</p> <p>Background</p> <p>Choroid plexus epithelial cells are the site of blood/cerebrospinal fluid (CSF) barrier and regulate molecular transfer between the two compartments. Their mitotic activity in the adult is low. During development, the pattern of growth and timing of acquisition of functional properties of plexus epithelium are not known.</p> <p>Methods</p> <p>Numbers and size of choroid plexus epithelial cells and their nuclei were counted and measured in the lateral ventricular plexus from the first day of its appearance until adulthood. Newborn <it>Monodelphis </it>pups were injected with 5-bromo-2-deoxyuridine (BrdU) at postnatal day 3 (P3), P4 and P5. Additional animals were injected at P63, P64 and P65. BrdU-immunopositive nuclei were counted and their position mapped in the plexus structure at different ages after injections. Double-labelling immunocytochemistry with antibodies to plasma protein identified post-mitotic cells involved in protein transfer.</p> <p>Results</p> <p>Numbers of choroid plexus epithelial cells increased 10-fold between the time of birth and adulthood. In newborn pups each consecutive injection of BrdU labelled 20-40 of epithelial cells counted. After 3 injections, numbers of BrdU positive cells remained constant for at least 2 months. BrdU injections at an older age (P63, P64, P65) resulted in a smaller number of labelled plexus cells. Numbers of plexus cells immunopositive for both BrdU and plasma protein increased with age indicating that protein transferring properties are acquired post mitotically. Labelled nuclei were only detected on the dorsal arm of the plexus as it grows from the neuroependyma, moving along the structure in a 'conveyor belt' like fashion.</p> <p>Conclusions</p> <p>The present study established that lateral ventricular choroid plexus epithelial cells are born on the dorsal side of the structure only. Cells born in the first few days after choroid plexus differentiation from the neuroependyma remain present even two months later. Protein-transferring properties are acquired post-mitotically and relatively early in plexus development.</p