This paper presents the first cosmological results based on Planck measurements of the cosmic microwave background (CMB) temperature and lensing-potential power spectra. We find that the Planck spectra at high multipoles ( > ∼ 40) are extremely well described by the standard spatiallyflat six-parameter ΛCDM cosmology with a power-law spectrum of adiabatic scalar perturbations. Within the context of this cosmology, the Planck data determine the cosmological parameters to high precision: the angular size of the sound horizon at recombination, the physical densities of baryons and cold dark matter, and the scalar spectral index are estimated to be θ * = (1.04147 ± 0.00062) × 10 −2 , Ω b h 2 = 0.02205 ± 0.00028, Ω c h 2 = 0.1199 ± 0.0027, and n s = 0.9603 ± 0.0073, respectively (note that in this abstract we quote 68% errors on measured parameters and 95% upper limits on other parameters). For this cosmology, we find a low value of the Hubble constant, H 0 = (67.3 ± 1.2) km s −1 Mpc −1 , and a high value of the matter density parameter, Ω m = 0.315 ± 0.017. These values are in tension with recent direct measurements of H 0 and the magnituderedshift relation for Type Ia supernovae, but are in excellent agreement with geometrical constraints from baryon acoustic oscillation (BAO) surveys. Including curvature, we find that the Universe is consistent with spatial flatness to percent level precision using Planck CMB data alone. We use high-resolution CMB data together with Planck to provide greater control on extragalactic foreground components in an investigation of extensions to the six-parameter ΛCDM model. We present selected results from a large grid of cosmological models, using a range of additional astrophysical data sets in addition to Planck and high-resolution CMB data. None of these models are favoured over the standard six-parameter ΛCDM cosmology. The deviation of the scalar spectral index from unity is insensitive to the addition of tensor modes and to changes in the matter content of the Universe. We find an upper limit of r 0.002 < 0.11 on the tensor-to-scalar ratio. There is no evidence for additional neutrino-like relativistic particles beyond the three families of neutrinos in the standard model. Using BAO and CMB data, we find N eff = 3.30 ± 0.27 for the effective number of relativistic degrees of freedom, and an upper limit of 0.23 eV for the sum of neutrino masses. Our results are in excellent agreement with big bang nucleosynthesis and the standard value of N eff = 3.046. We find no evidence for dynamical dark energy; using BAO and CMB data, the dark energy equation of state parameter is constrained to be w = −1.13 +0.13 −0.10 . We also use the Planck data to set limits on a possible variation of the fine-structure constant, dark matter annihilation and primordial magnetic fields. Despite the success of the six-parameter ΛCDM model in describing the Planck data at high multipoles, we note that this cosmology does not provide a good fit to the temperature power spectrum at low multipoles. T...
We report the results of a joint analysis of data from BICEP2/Keck Array and Planck. BICEP2 and Keck Array have observed the same approximately 400 deg 2 patch of sky centered on RA 0 h, Dec. −57.5°. The combined maps reach a depth of 57 nK deg in Stokes Q and U in a band centered at 150 GHz. Planck has observed the full sky in polarization at seven frequencies from 30 to 353 GHz, but much less deeply in any given region (1.2 μK deg in Q and U at 143 GHz). We detect 150 × 353 cross-correlation in B modes at high significance. We fit the single-and cross-frequency power spectra at frequencies ≥ 150 GHz to a lensed-ΛCDM model that includes dust and a possible contribution from inflationary gravitational waves (as parametrized by the tensor-to-scalar ratio r), using a prior on the frequency spectral behavior of polarized dust emission from previous Planck analysis of other regions of the sky. We find strong evidence for dust and no statistically significant evidence for tensor modes. We probe various model variations and extensions, including adding a synchrotron component in combination with lower frequency data, and find that these make little difference to the r constraint. Finally, we present an alternative analysis which is similar to a map-based cleaning of the dust contribution, and show that this gives similar constraints. The final result is expressed as a likelihood curve for r, and yields an upper limit r 0.05 < 0.12 at 95% confidence. Marginalizing over dust and r, lensing B modes are detected at 7.0σ significance.
We analyse the implications of the Planck data for cosmic inflation. The Planck nominal mission temperature anisotropy measurements, combined with the WMAP large-angle polarization, constrain the scalar spectral index to be n s = 0.9603 ± 0.0073, ruling out exact scale invariance at over 5σ. Planck establishes an upper bound on the tensor-to-scalar ratio of r < 0.11 (95% CL). The Planck data thus shrink the space of allowed standard inflationary models, preferring potentials with V < 0. Exponential potential models, the simplest hybrid inflationary models, and monomial potential models of degree n ≥ 2 do not provide a good fit to the data. Planck does not find statistically significant running of the scalar spectral index, obtaining dn s /dln k = −0.0134 ± 0.0090. We verify these conclusions through a numerical analysis, which makes no slowroll approximation, and carry out a Bayesian parameter estimation and model-selection analysis for a number of inflationary models including monomial, natural, and hilltop potentials. For each model, we present the Planck constraints on the parameters of the potential and explore several possibilities for the post-inflationary entropy generation epoch, thus obtaining nontrivial data-driven constraints. We also present a direct reconstruction of the observable range of the inflaton potential. Unless a quartic term is allowed in the potential, we find results consistent with second-order slow-roll predictions. We also investigate whether the primordial power spectrum contains any features. We find that models with a parameterized oscillatory feature improve the fit by ∆χ 2 eff ≈ 10; however, Bayesian evidence does not prefer these models. We constrain several single-field inflation models with generalized Lagrangians by combining power spectrum data with Planck bounds on f NL. Planck constrains with unprecedented accuracy the amplitude and possible correlation (with the adiabatic mode) of non-decaying isocurvature fluctuations. The fractional primordial contributions of cold dark matter (CDM) isocurvature modes of the types expected in the curvaton and axion scenarios have upper bounds of 0.25% and 3.9% (95% CL), respectively. In models with arbitrarily correlated CDM or neutrino isocurvature modes, an anticorrelated isocurvature component can improve the χ 2 eff by approximately 4 as a result of slightly lowering the theoretical prediction for the < ∼ 40 multipoles relative to the higher multipoles. Nonetheless, the data are consistent with adiabatic initial conditions.
We have examined the structure and expression of the products associated with the t(2;13)(q35;q14) translocation associated with alveolar rhabdomyosarcoma. The chromosome 13 gene (FKHR) is identified as a member of the fork head domain family of transcription factors characterized by a conserved DNA binding motif. Polymerase chain reaction analysis demonstrates that a 5'PAX3-3' FKHR chimaeric transcript is expressed in all eight alveolar rhabdomyosarcomas investigated. Immunoprecipitation experiments detect the predicted fusion protein. These findings indicate that the t(2;13) generates a potentially tumorigenic fusion transcription factor consisting of intact PAX3 DNA binding domains, a truncated fork head DNA binding domain and C-terminal FKHR regions.
A full-sky template map of the Galactic free-free foreground emission component is increasingly important for high sensitivity CMB experiments. We use the recently published \ha data of both the northern and southern skies as the basis for such a template. The first step is to correct the \ha maps for dust absorption using the 100 $\mu$m dust maps of Schlegel, Finkbeiner & Davis (1998). We show that for a range of longitudes, the Galactic latitude distribution of absorption suggests that it is 33 per cent of the full extragalactic absorption. A reliable absorption-corrected \ha map can be produced for $\sim 95$ per cent of the sky; the area for which a template cannot be recovered is the Galactic plane area $|b| < 5^{\circ}$, $l=260^{\circ}-0^{\circ}-160^{\circ}$ and some isolated dense dust clouds at intermediate latitudes. The second step is to convert the dust-corrected \ha data into a predicted radio surface brightness. The free-free emission formula is revised to give an accurate expression (1 per cent) for the radio emission covering the frequency range 100 MHz to 100 GHz and the electron temperature range 3000 to 20000 K. The main uncertainty when applying this expression is the variation of electron temperature across the sky. The emission formula is verified in several extended H{\sc ii} regions using data in the range 408 to 2326 MHz. A full-sky free-free template map is presented at 30 GHz; the scaling to other frequencies is given. The Haslam et al. all-sky 408 MHz map of the sky can be corrected for this free-free component, which amounts to a $\approx 6$ per cent correction at intermediate and high latitudes....Comment: 18 pages, 11 figures, accepted for publication in M.N.R.A.S. High-resolution versions of figs 2,7 (in colour), 9 and 11 can be obtained from ftp://ftp.jb.man.ac.uk/pub/cdickins/ff_paper/FINAL_FIGURES
The Planck nominal mission cosmic microwave background (CMB) maps yield unprecedented constraints on primordial non-Gaussianity (NG). Using three optimal bispectrum estimators, separable template-fitting (KSW), binned, and modal, we obtain consistent values for the primordial local, equilateral, and orthogonal bispectrum amplitudes, quoting as our final result f local NL = 2.7 ± 5.8, f equil NL = −42 ± 75, and f ortho NL = −25 ± 39 (68% CL statistical). Non-Gaussianity is detected in the data; using skew-C statistics we find a nonzero bispectrum from residual point sources, and the integrated-Sachs-Wolfe-lensing bispectrum at a level expected in the ΛCDM scenario. The results are based on comprehensive crossvalidation of these estimators on Gaussian and non-Gaussian simulations, are stable across component separation techniques, pass an extensive suite of tests, and are confirmed by skew-C , wavelet bispectrum and Minkowski functional estimators. Beyond estimates of individual shape amplitudes, we present model-independent, three-dimensional reconstructions of the Planck CMB bispectrum and thus derive constraints on early-Universe scenarios that generate primordial NG, including general single-field models of inflation, excited initial states (non-Bunch-Davies vacua), and directionally-dependent vector models. We provide an initial survey of scale-dependent feature and resonance models. These results bound both general single-field and multi-field model parameter ranges, such as the speed of sound, c s ≥ 0.02 (95% CL), in an effective field theory parametrization, and the curvaton decay fraction r D ≥ 0.15 (95% CL). The Planck data significantly limit the viable parameter space of the ekpyrotic/cyclic scenarios. The amplitude of the four-point function in the local model τ NL < 2800 (95% CL). Taken together, these constraints represent the highest precision tests to date of physical mechanisms for the origin of cosmic structure.
The two fundamental assumptions of the standard cosmological model -that the initial fluctuations are statistically isotropic and Gaussian -are rigorously tested using maps of the cosmic microwave background (CMB) anisotropy from the Planck satellite. The detailed results are based on studies of four independent estimates of the CMB that are compared to simulations using a fiducial ΛCDM model and incorporating essential aspects of the Planck measurement process. Deviations from isotropy have been found and demonstrated to be robust against component separation algorithm, mask choice, and frequency dependence. Many of these anomalies were previously observed in the WMAP data, and are now confirmed at similar levels of significance (about 3σ). However, we find little evidence of non-Gaussianity, with the exception of a few statistical signatures that seem to be associated with specific anomalies. In particular, we find that the quadrupole-octopole alignment is also connected to a low observed variance in the CMB signal. A power asymmetry is now found to persist on scales corresponding to about = 600 and can be described in the low-regime by a phenomenological dipole modulation model. However, any primordial power asymmetry is strongly scale-dependent and does not extend to arbitrarily small angular scales. Finally, it is plausible that some of these features may be reflected in the angular power spectrum of the data, which shows a deficit of power on similar scales. Indeed, when the power spectra of two hemispheres defined by a preferred direction are considered separately, one shows evidence of a deficit in power, while its opposite contains oscillations between odd and even modes that may be related to the parity violation and phase correlations also detected in the data. Although these analyses represent a step forward in building an understanding of the anomalies, a satisfactory explanation based on physically motivated models is still lacking.
We have identified a novel vertebrate homolog of the Drosophila gene dachshund, Dachshund2 (Dach2).Dach2 is expressed in the developing somite prior to any myogenic genes with an expression profile similar to Pax3, a gene previously shown to induce muscle differentiation. Pax3 and Dach2 participate in a positive regulatory feedback loop, analogous to a feedback loop that exists in Drosophila between the Pax gene eyeless (a Pax6 homolog) and the Drosophila dachshund gene. Although Dach2 alone is unable to induce myogenesis, Dach2 can synergize with Eya2 (a vertebrate homolog of the Drosophila gene eyes absent) to regulate myogenic differentiation. Moreover, Eya2 can also synergize with Six1 (a vertebrate homolog of the Drosophila gene sine oculis) to regulate myogenesis. This synergistic regulation of muscle development by Dach2 with Eya2 and Eya2 with Six1 parallels the synergistic regulation of Drosophila eye formation by dachshund with eyes absent and eyes absent with sine oculis. This synergistic regulation is explained by direct physical interactions between Dach2 and Eya2, and Eya2 and Six1 proteins, analogous to interactions observed between the Drosophila proteins. This study reveals a new layer of regulation in the process of myogenic specification in the somites. Moreover, we show that the Pax, Dach, Eya, and Six genetic network has been conserved across species. However, this genetic network has been used in a novel developmental context, myogenesis rather than eye development, and has been expanded to include gene family members that are not directly homologous, for example Pax3 instead of Pax6. [Key Words: Dach2; Eya2; Six1; Pax3; myogenesis; dachshund; somite development] Received August 20, 1999; revised version accepted November 1, 1999. Somites are segmentally organized mesodermal structures that are the embryonic precursors of the axial skeleton and of all skeletal muscle (for review, see Christ and Ordahl 1995). Somites form by budding off from the anterior end of the presegmental mesoderm (PSM) to form epithelial balls of tissue. Patterning signals from surrounding tissues induce different regions of the somite to acquire distinct fates: The dorsal somite develops into the dermamyotome, the precursor to the dermis and to the muscles; and the ventral somite gives rise to the sclerotome, the precursor of the axial skeleton and ribs (Christ and Ordahl 1995). Subsequent inductive signaling leads to further subdivision of cell fates within the somite.The best studied aspect of this patterning and differentiation process is the specification of the myogenic cells. The establishment of muscle cell fate requires inductive signals both from axial tissues and from the dorsal ectoderm that overlays the somite (Christ and Ordahl 1995;Cossu et al. 1996). The progress of myogenic induction can be observed by following the expression of the paired-type transcription factor Pax3. In the chick embryo, Pax3 is initially expressed throughout the PSM (Williams and Ordahl 1994). However, early inductive infl...
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