Searcharxiv⌕ Search

arXiv subjects

Le Zhang

Publications and source records attributed to Le Zhang.

266 records · Page 15Linked to original sources

Systematic Effects in Interferometric Observations of the CMB Polarization

The detection of the primordial $B$-mode spectrum of the polarized cosmic microwave background (CMB) signal may provide a probe of inflation. However, observation of such a faint signal requires excellent control of systematic errors. Interferometry proves to be a promising approach for overcoming such a challenge. In this paper we present a complete simulation pipeline of interferometric observations of CMB polarization, including systematic errors. We employ two different methods for obtaining the power spectra from mock data produced by simulated observations: the maximum likelihood method and the method of Gibbs sampling. We show that the results from both methods are consistent with each other, as well as, within a factor of 6, with analytical estimates. Several categories of systematic errors are considered: instrumental errors, consisting of antenna gain and antenna coupling errors, and beam errors, consisting of antenna pointing errors, beam cross-polarization and beam shape (and size) errors. In order to recover the tensor-to-scalar ratio, $r$, within a 10% tolerance level, which ensures the experiment is sensitive enough to detect the $B$-signal at $r=0.01$ in the multipole range $28 < \ell < 384$, we find that, for a QUBIC-like experiment, Gaussian-distributed systematic errors must be controlled with precisions of $|g_{rms}| = 0.1$ for antenna gain, $|ε_{rms}| = 5 \times 10^{-4}$ for antenna coupling, $δ_{rms} \approx 0.7^\circ$ for pointing, $ζ_{rms} \approx 0.7^\circ$ for beam shape, and $μ_{rms} = 5 \times 10^{-4}$ for beam cross-polarization.

astro-ph.CO↗

Bayesian Inference of Polarized CMB Power Spectra from Interferometric Data

Detection of B-mode polarization of the cosmic microwave background (CMB) radiation is one of the frontiers of observational cosmology. Because they are an order of magnitude fainter than E-modes, it is quite a challenge to detect B-modes. Having more manageable systematics, interferometers prove to have a substantial advantage over imagers in detecting such faint signals. Here, we present a method for Bayesian inference of power spectra and signal reconstruction from interferometric data of the CMB polarization signal by using the technique of Gibbs sampling. We demonstrate the validity of the method in the flat-sky approximation for a simulation of an interferometric observation on a finite patch with incomplete uv-plane coverage, a finite beam size and a realistic noise model. With a computational complexity of O(n^{3/2}), n being the data size, Gibbs sampling provides an efficient method for analyzing upcoming cosmology observations.

astro-ph.CO↗

Indirect searches of dark matter

If dark matter decays or annihilates into electrons and positrons, it can affect radiation and cosmic-ray backgrounds. We review a novel, more general analysis of constraints on decaying dark matter models, by introducing the response functions based on the current radio, gamma-ray and positron observations. Constraints can be simply obtained by requiring the convolution of the response functions with actual decay spectrum of electrons and positrons smaller than the product of decay lifetime in 10^{26}s and mass in 100GeV. The response functions just depend on the astrophysical inputs such as the propagation model, but not on the microscopic decay scenario. Moreover, an anisotropy analysis of the full-sky radio emissions to identify the extragalactic dark matter annihilation is shown. We discuss the angular power spectra of the cosmological synchrotron emission from dark matter annihilations into electron positron pairs and compare them with astrophysical backgrounds and Galactic foregrounds. We find that the angular power spectrum of radio fluxes at around GHz frequencies and in the range of 200 <l <3000 opens a optimal window to disentangle the dark matter signals from common astrophysical backgrounds.

astro-ph.CO↗

Inverse Compton gamma-rays from Galactic dark matter annihilation: Anisotropy signatures

High energy electrons and positrons from annihilating dark matter can imprint unique angular anisotropies on the diffuse gamma-ray flux by inverse Compton scattering off the interstellar radiation field. We develop a numerical tool to compute gamma-ray emission from such electrons and positrons produced in the smooth host halo and in substructure halos with masses down to 10^(-6)M_sun. We show that the angular power spectrum from inverse Compton scattering is exponentially suppressed below an angular scale determined by the diffusion length of electrons and positrons. We also find that the total flux and the shape of the angular power spectrum depends sensitively on the spatial distribution of subhalos in the Milky Way. Finally, the contribution from the smooth host halo component to the gamma-ray mean intensity is negligibly small compared to subhalos.

astro-ph.HE↗

Constraining Decaying Dark Matter with Fermi LAT Gamma-rays

High energy electrons and positrons from decaying dark matter can produce a significant flux of gamma rays by inverse Compton off low energy photons in the interstellar radiation field. This possibility is inevitably related with the dark matter interpretation of the observed PAMELA and FERMI excesses. The aim of this paper is providing a simple and universal method to constraint dark matter models which produce electrons and positrons in their decay by using the Fermi LAT gamma-ray observations in the energy range between 0.5 GeV and 300 GeV. We provide a set of universal response functions that, once convolved with a specific dark matter model produce the desired constraint. Our response functions contain all the astrophysical inputs such as the electron propagation in the galaxy, the dark matter profile, the gamma-ray fluxes of known origin, and the Fermi LAT data. We study the uncertainties in the determination of the response functions and apply them to place constraints on some specific dark matter decay models that can well fit the positron and electron fluxes observed by PAMELA and Fermi LAT. To this end we also take into account prompt radiation from the dark matter decay. We find that with the available data decaying dark matter cannot be excluded as source of the PAMELA positron excess.

astro-ph.HE↗

Galactic Signatures of Decaying Dark Matter

If dark matter decays into electrons and positrons, it can affect Galactic radio emissions and the local cosmic ray fluxes. We propose a new, more general analysis of constraints on dark matter. The constraints can be obtained for any decaying dark matter model by convolving the specific dark matter decay spectrum with a response function. We derive this response function from full-sky radio surveys at 408 MHz, 1.42 GHz and 23 GHz, as well as from the positron flux recently reported by PAMELA. We discuss the influence of astrophysical uncertainties on the response function, such as from propagation and from the profiles of the dark matter and the Galactic magnetic field. As an application, we find that some widely used dark matter decay scenarios can be ruled out under modest assumptions.

astro-ph.GA↗

Dark Matter Signatures in the Anisotropic Radio Sky

We calculate intensity and angular power spectrum of the cosmological background of synchrotron emission from cold dark matter annihilations into electron positron pairs. We compare this background with intensity and anisotropy of astrophysical and cosmological radio backgrounds, such as from normal galaxies, radio-galaxies, galaxy cluster accretion shocks, the cosmic microwave background and with Galactic foregrounds. Under modest assumptions for the dark matter clustering we find that around 2 GHz average intensity and fluctuations of the radio background at sub-degree scales allows to probe dark matter masses >100 GeV and annihilation cross sections not far from the natural values ~ 3 x 10^(-26) cm^3/s required to reproduce the correct relic density of thermal dark matter. The angular power spectrum of the signal from dark matter annihilation tends to be flatter than that from astrophysical radio backgrounds. Furthermore, radio source counts have comparable constraining power. Such signatures are interesting especially for future radio detectors such as SKA.

astro-ph↗

Cancer Cell Motility: Optimizing Spatial Search Strategies

Aberrantly regulated cell motility is a hallmark of cancer cells. A hybrid agent-based model has been developed to investigate the synergistic and antagonistic cell motility-impacting effects of three microenvironment variables simultaneously: chemoattraction, haptotactic permission, and biomechanical constraint or resistance. Reflecting distinct cell-specific intracellular machinery, the cancer cells are modelled as processing a variety of spatial search strategies that respond to these three influencing factors with differential weights attached to each. While responding exclusively to chemoattraction optimizes cell displacement effectiveness, incorporating permission and resistance components becomes increasingly important with greater distance to the chemoattractant source and/or after reducing the ligand's effective diffusion coefficient. Extending this to a heterogeneous population of cells shows that displacement effectiveness increases with clonal diversity as characterized by the Shannon index. However, the resulting data can be fit best to an exponential function, suggesting that there is a level of population heterogeneity beyond which its added value to the cancer system becomes minimal as directionality ceases to increase. Possible experimental extensions and potential clinical implications are discussed.

q-bio.CB↗

Multi-Scale, Multi-Resolution Brain Cancer Modeling

In advancing discrete-based computational cancer models towards clinical applications, one faces the dilemma of how to deal with an ever growing amount of biomedical data that ought to be incorporated eventually in one form or another. Model scalability becomes of paramount interest. In an effort to start addressing this critical issue, here, we present a novel multi-scale and multi-resolution agent-based in silico glioma model. While "multi-scale" refers to employing an epidermal growth factor receptor (EGFR)-driven molecular network to process cellular phenotypic decisions within the micro-macroscopic environment, "multi-resolution" is achieved through algorithms that classify cells to either active or inactive spatial clusters, which determine the resolution they are simulated at. The aim is to assign computational resources where and when they matter most for maintaining or improving the predictive power of the algorithm, onto specific tumor areas and at particular times. Using a previously described 2D brain tumor model, we have developed four different computational methods for achieving the multi-resolution scheme, three of which are designed to dynamically train on the high-resolution simulation that serves as control. To quantify the algorithms' performance, we rank them by weighing the distinct computational time savings of the simulation runs versus the methods' ability to accurately reproduce the high-resolution results of the control. Finally, to demonstrate the flexibility of the underlying concept, we show the added value of combining the two highest-ranked methods.

q-bio.CB↗

Contraints on radiative dark-matter decay from the cosmic microwave background

If dark matter decays to electromagnetically-interacting particles, it can inject energy into the baryonic gas and thus affect the processes of recombination and reionization. This leaves an imprint on the cosmic microwave background (CMB): the large-scale polarization is enhanced, and the small-scale temperature fluctuation is damped. We use the WMAP three-year data combined with galaxy surveys to constrain radiatively decaying dark matter. Our new limits to the dark-matter decay width are about ten times stronger than previous limits. For dark-matter lifetimes that exceed the age of the Universe, a limit of $ζΓ_χ < 1.7 \times 10^{-25} s^{-1}$ (95% CL) is derived, where $ζ$ is the efficiency of converting decay energy into ionization energy. Limits for lifetimes short compared with the age of the Universe are also derived. We forecast improvements expected from the Planck satellite.

astro-ph↗

Simulating Brain Tumor Heterogeneity with a Multiscale Agent-Based Model: Linking Molecular Signatures, Phenotypes and Expansion Rate

We have extended our previously developed 3D multi-scale agent-based brain tumor model to simulate cancer heterogeneity and to analyze its impact across the scales of interest. While our algorithm continues to employ an epidermal growth factor receptor (EGFR) gene-protein interaction network to determine the cells' phenotype, it now adds an explicit treatment of tumor cell adhesion related to the model's biochemical microenvironment. We simulate a simplified tumor progression pathway that leads to the emergence of five distinct glioma cell clones with different EGFR density and cell 'search precisions'. The in silico results show that microscopic tumor heterogeneity can impact the tumor system's multicellular growth patterns. Our findings further confirm that EGFR density results in the more aggressive clonal populations switching earlier from proliferation-dominated to a more migratory phenotype. Moreover, analyzing the dynamic molecular profile that triggers the phenotypic switch between proliferation and migration, our in silico oncogenomics data display spatial and temporal diversity in documenting the regional impact of tumorigenesis, and thus support the added value of multi-site and repeated assessments in vitro and in vivo. Potential implications from this in silico work for experimental and computational studies are discussed.

q-bio.TO↗

Simulating non-small cell lung cancer with a multiscale agent-based model

Background The epidermal growth factor receptor (EGFR) is frequently overexpressed in many cancers, including non-small cell lung cancer (NSCLC). In silcio modeling is considered to be an increasingly promising tool to add useful insights into the dynamics of the EGFR signal transduction pathway. However, most of the previous modeling work focused on the molecular or the cellular level only, neglecting the crucial feedback between these scales as well as the interaction with the heterogeneous biochemical microenvironment. Results We developed a multiscale model for investigating expansion dynamics of NSCLC within a two-dimensional in silico microenvironment. At the molecular level, a specific EGFR-ERK intracellular signal transduction pathway was implemented. Dynamical alterations of these molecules were used to trigger phenotypic changes at the cellular level. Examining the relationship between extrinsic ligand concentrations, intrinsic molecular profiles and microscopic patterns, the results confirmed that increasing the amount of available growth factor leads to a spatially more aggressive cancer system. Moreover, for the cell closest to nutrient abundance, a phase-transition emerges where a minimal increase in extrinsic ligand abolishes the proliferative phenotype altogether. Conclusions Our in silico results indicate that, in NSCLC, in the presence of a strong extrinsic chemotactic stimulus, and depending on the cell's location, downstream EGFR-ERK signaling may be processed more efficiently, thereby yielding a migration-dominant cell phenotype and overall, an accelerated spatio-temporal expansion rate.

q-bio.CB↗

The impacts of dark matter particle annihilation on recombination and the anisotropies of the cosmic microwave background

The recombination history of the Universe provides a useful tool for constraining the annihilation of dark matter particles. Even a small fraction of dark matter particles annihilated during the cosmic dark age can provide sufficient energy to affect the ionization state of the baryonic gas. Although this effect is too small for neutralinos, lighter dark matter particle candidates, e.g. with mass of 1-100 MeV, which was proposed recently to explain the observed excess of positrons in the Galactic Center, may generate observable differences in the cosmic microwave background (CMB) temperature and polarization anisotropies. The annihilations at the era of recombination affects mainly the CMB anisotropy at small angular scales (large $\ell$), and is distinctively different from the effect of early reionization. We perform a multi-parameter analysis of the CMB data, including the both the WMAP first year and three year data, and the ACBAR, Boomerang, CBI, and VSA data. Assuming that the observed excess of $e^+e^-$ pairs in the galactic center region is produced by dark matter annihilation, and that a sizable fraction of the energy produced in the annihilation is deposited in the baryonic gas during recombination, we obtain a %95 dark matter mass limit of $M<8 \MeV$ with the current data set.

astro-ph↗

Development of a Three-Dimensional Multiscale Agent-Based Tumor Model: Simulating Gene-Protein Interaction Profiles, Cell Phenotypes & Multicellular Patterns in Brain Cancer

Experimental evidence suggests that epidermal growth factor receptor (EGFR)-mediated activation of the signaling protein phospholipase C gamma plays a critical role in a cancer cell's phenotypic decision to either proliferate or to migrate at a given point in time. Here, we present a novel three-dimensional multiscale agent-based model to simulate this cellular decision process in the context of a virtual brain tumor. Each tumor cell is equipped with an EGFR gene-protein interaction network module that also connects to a simplified cell cycle description. The simulation results show that over time proliferative and migratory cell populations not only oscillate but also directly impact the spatio-temporal expansion patterns of the entire cancer system. The percentage change in the concentration of the sub-cellular interaction network's molecular components fluctuates, and, for the proliferation-to-migration switch we find that the phenotype triggering molecular profile to some degree varies as the tumor system grows and the microenvironment changes. We discuss potential implications of these findings for experimental and clinical cancer research.

q-bio.TO↗