57 research outputs found
Aspherical supernova explosions and formation of compact black hole low-mass X-ray binaries
It has been suggested that black-hole low-mass X-ray binaries (BHLMXBs) with
short orbital periods may have evolved from BH binaries with an
intermediate-mass secondary, but the donor star seems to always have higher
effective temperatures than measured in BHLMXBs (Justham, Rappaport &
Podsiadlowski 2006). Here we suggest that the secondary star is originally an
intermediate-mass (\sim 2-5 M_{\sun}) star, which loses a large fraction of
its mass due to the ejecta impact during the aspherical SN explosion that
produced the BH. The resulted secondary star could be of low-mass (\la 1
M_{\sun}). Magnetic braking would shrink the binary orbit, drive mass transfer
between the donor and the BH, producing a compact BHLMXB.Comment: 4 pages, accepted for publication in MNRAS Letter
Bridging ultrahigh-Q devices and photonic circuits
Optical microresonators are essential to a broad range of technologies and scientific disciplines. However, many of their applications rely on discrete devices to attain challenging combinations of ultra-low-loss performance (ultrahigh Q) and resonator design requirements. This prevents access to scalable fabrication methods for photonic integration and lithographic feature control. Indeed, finding a microfabrication bridge that connects ultrahigh-Q device functions with photonic circuits is a priority of the microcavity field. Here, an integrated resonator having a record Q factor over 200 million is presented. Its ultra-low-loss and flexible cavity design brings performance to integrated systems that has been the exclusive domain of discrete silica and crystalline microcavity devices. Two distinctly different devices are demonstrated: soliton sources with electronic repetition rates and high-coherence/low-threshold Brillouin lasers. This multi-device capability and performance from a single integrated cavity platform represents a critical advance for future photonic circuits and systems
A Systems Approach for Tumor Pharmacokinetics
Recent advances in genome inspired target discovery, small molecule screens, development of biological and nanotechnology have led to the introduction of a myriad of new differently sized agents into the clinic. The differences in small and large molecule delivery are becoming increasingly important in combination therapies as well as the use of drugs that modify the physiology of tumors such as anti-angiogenic treatment. The complexity of targeting has led to the development of mathematical models to facilitate understanding, but unfortunately, these studies are often only applicable to a particular molecule, making pharmacokinetic comparisons difficult. Here we develop and describe a framework for categorizing primary pharmacokinetics of drugs in tumors. For modeling purposes, we define drugs not by their mechanism of action but rather their rate-limiting step of delivery. Our simulations account for variations in perfusion, vascularization, interstitial transport, and non-linear local binding and metabolism. Based on a comparison of the fundamental rates determining uptake, drugs were classified into four categories depending on whether uptake is limited by blood flow, extravasation, interstitial diffusion, or local binding and metabolism. Simulations comparing small molecule versus macromolecular drugs show a sharp difference in distribution, which has implications for multi-drug therapies. The tissue-level distribution differs widely in tumors for small molecules versus macromolecular biologic drugs, and this should be considered in the design of agents and treatments. An example using antibodies in mouse xenografts illustrates the different in vivo behavior. This type of transport analysis can be used to aid in model development, experimental data analysis, and imaging and therapeutic agent design.National Institutes of Health (U.S.) (grant T32 CA079443
Rab32 connects ER stress to mitochondrial defects in multiple sclerosis.
Endoplasmic reticulum (ER) stress is a hallmark of neurodegenerative diseases such as multiple sclerosis (MS). However, this physiological mechanism has multiple manifestations that range from impaired clearance of unfolded proteins to altered mitochondrial dynamics and apoptosis. While connections between the triggering of the unfolded protein response (UPR) and downstream mitochondrial dysfunction are poorly understood, the membranous contacts between the ER and mitochondria, called the mitochondria-associated membrane (MAM), could provide a functional link between these two mechanisms. Therefore, we investigated whether the guanosine triphosphatase (GTPase) Rab32, a known regulator of the MAM, mitochondrial dynamics, and apoptosis, could be associated with ER stress as well as mitochondrial dysfunction.This article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site
Fast and Inexpensive Detection of Total and Extractable Element Concentrations in Aquatic Sediments Using Near-Infrared Reflectance Spectroscopy (NIRS)
Contains fulltext :
116994.pdf (publisher's version ) (Open Access
The convective Urca process
One possible fate of an accreting white dwarf is explosion in a type Ia
supernova. However, the route to the thermonuclear runaway has always been
uncertain owing to the lack of a convective model consistent with the Urca
process.
We derive a formalism for convective motions involving two radial flows. This
formalism provides a framework for convective models that guarantees
self-consistency for chemistry and energy budget, allows time-dependence and
describes the interaction of convective motions with the global contraction or
expansion of the star. In the one-stream limit, we reproduce several already
existing convective models and allow them to treat chemistry. We also suggest
as a model easy to implement in a stellar evolution code.
We apply this formalism to convective Urca cores in Chandrasekhar mass white
dwarfs. We stress that in degenerate matter, nuclear reactions that change the
number of electrons strongly influence the convective velocities. We point out
the sensitivity of the energy budget on the mixing. We illustrate our model by
computing {\it stationary} convective cores with Urca nuclei. We show that even
a very small mass fraction of Urca nuclei () strongly influences the
convective velocities.
Finally, we present preliminary computations of the late evolution of a close
to Chandrasekhar mass C+O white dwarf including the convective Urca process
Zusammenhänge zwischen physikalischen und chemischen Vorgängen bei der Muskelkontraktion
Vergleichende Untersuchungen �ber die Spontanoxydation von Nabelschnur- und Erwachsenenh�moglobin
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