39 research outputs found
Scale-dependent non-Gaussianity and the CMB power asymmetry
We introduce an alternative parametrisation for the scale dependence of the non–linearity parameter fNL in quasi-local models of non–Gaussianity. Our parametrisation remains valid when fNL changes sign, unlike the commonly adopted power law ansatz fNL(k) ∝ knfNL. We motivate our alternative parametrisation by appealing to the self-interacting curvaton scenario, and as an application, we apply it to the CMB power asymmetry. Explaining the power asymmetry requires a strongly scale dependent non-Gaussianity. We show that regimes of model parameter space where fNL is strongly scale dependent are typically associated with a large gNL and quadrupolar power asymmetry, which can be ruled out by existing observational constraints
Inflationary signatures of single-field models beyond slow-roll
If the expansion of the early Universe was not close to de Sitter, the
statistical imprints of the primordial density perturbation on the cosmic
microwave background can be quite different from those derived in slow-roll
inflation. In this paper we study the inflationary signatures of all
single-field models which are free of ghost-like instabilities. We allow for a
rapid change of the Hubble parameter and the speed of sound of scalar
fluctuations, in a way that is compatible with a nearly scale-invariant
spectrum of perturbations, as supported by current cosmological observations.
Our results rely on the scale-invariant approximation, which is different from
the standard slow-roll approximation. We obtain the propagator of scalar
fluctuations and compute the bispectrum, keeping next-order corrections
proportional to the deviation of the spectral index from unity. These theories
offer an explicit example where the shape and scale-dependences of the
bispectrum are highly non-trivial whenever slow-roll is not a good
approximation.Comment: v1: 36 pages, including tables, appendices and references. v2:
abstract improved, references added, minor clarifications throughout the
text; matches version published in JCA
The hemispherical asymmetry from a scale-dependent inflationary bispectrum
If the primordial bispectrum is sufficiently large then the CMB hemispherical asymmetry may be explained by a large-scale mode of exceptional amplitude which perturbs the zeta two-point function. We extend previous calculations, which were restricted to one- or two-source scenarios, by providing a method to compute the response of the two-point function in any model yielding a 'local-like' bispectrum. In general, this shows that it is not the reduced bispectrum fNL which sources the amplitude and scale-dependence of the mode coupling but rather a combination of 'response functions'. We discuss why it is difficult to construct successful scenarios and enumerate the fine-tunings which seem to be required. Finally, we exhibit a concrete model which can be contrived to match the observational constraints and show that to a Planck-like experiment it would appear to have |fNL-local| ~ |fNL-equi| ~ |fNL-ortho| ~ 1. Therefore, contrary to previous analyses, we conclude that it is possible to generate the asymmetry while respecting observational constraints on the bispectrum and low-ell multipoles even without tuning our location on the long-wavelength mode
Structures associated with feeding in three broad-mouthed, benthic fish groups
The flatheads, toadfishes, and goosefishes discussed here hold certain features in common. All are bottom-living forms with depressed head areas and broad gapes, and all eat large food items: fishes and/or crabs. All have developed structural specializations in association with this diet. The three groups are at most distantly related, and their feeding specializations are different and have evolved from different bases. In flatheads the combination of large food items and depressed head regions seems to have led to the separation of the two halves of the pelvic girdle, a feature in which they differ from their scorpaenoid relatives. Toadfish peculiarities associated with feeding are various but most notable in those that pass crabs they eat through the gape and into the mouth. Goosefish feeding is centered around the use of a lure to attract prey to within striking distance. The three fish groups are discussed separately, but their feeding structures are compared to one another in the final section of the paper.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42639/1/10641_2004_Article_BF00005053.pd
A possible relationship between aspects of dentition and feeding in the centrarchid and anabantoid fishes
Certain components of dentition — teeth on the third basibranchial in the Centrarchidae and on the parasphenoid in the anabantoids (sensu lato) — are very rare elsewhere in higher teleostean fishes. Though these basibranchial and parasphenoid teeth in the two fish groups are on opposite sides of the oral cavity, it is hypothesized that they both developed as adaptations for gripping a particular category of food items, namely strong-clawed, hard-shelled, active animals that, once within the oral cavity, would try to crawl out again. A corollary to this hypothesis is that higher teleosts with extensive dentition in the central part of the oral cavity have a grasping jaw bite, which, unlike a piercing, shearing, or crushing jaw bite, does not necessarily kill the prey that is taken into the oral cavity.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42630/1/10641_2004_Article_BF00005147.pd
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
Although multiple reports show that defective genetic networks underlie the aetiology of autism, few have translated into pharmacotherapeutic opportunities. Since drugs compete with endogenous small molecules for protein binding, many successful drugs target large gene families with multiple drug binding sites. Here we search for defective gene family interaction networks (GFINs) in 6,742 patients with the ASDs relative to 12,544 neurologically normal controls, to find potentially druggable genetic targets. We find significant enrichment of structural defects (P≤2.40E-09, 1.8-fold enrichment) in the metabotropic glutamate receptor (GRM) GFIN, previously observed to impact attention deficit hyperactivity disorder (ADHD) and schizophrenia. Also, the MXD-MYC-MAX network of genes, previously implicated in cancer, is significantly enriched (P≤3.83E-23, 2.5-fold enrichment), as is the calmodulin 1 (CALM1) gene interaction network (P≤4.16E-04, 14.4-fold enrichment), which regulates voltage-independent calcium-activated action potentials at the neuronal synapse. We find that multiple defective gene family interactions underlie autism, presenting new translational opportunities to explore for therapeutic interventions
�ber den Suspensionsmodus des Mandibularbogens und den splanchnischen Apparat beiStylephorus chordatus Shaw 1791 (Lampridiformes, Stylephoridae)
The status of Arctic charr Salvelinus alpinus in Britain and Ireland
The Arctic charr occurs in lakes across Britain and Ireland and was previously described here as 15 separate species. Most authorities now agree that all these stocks belong to a single polymorphic species complex Salvelinus alpinus (L.). This fish is given little protection in British and Irish law and there has been a steady loss of natural populations in recent years in all the countries concerned. A few new stocks have been created either intentionally or accidentally. In Scotland, only a small proportion of the 258 recorded natural populations has been studied and at least 12 of these are now extinct. There are at least four introduced populations originating from native Scottish stocks, but the fate of stocks introduced from Canada for aquaculture is uncertain. In England, there are eight extant populations in Cumbria and four others extinct. The status of introduced stocks in England is uncertain but there is probably one population surviving in Yorkshire. In Wales, eight lakes with resident Arctic charr populations have been recorded, three of these populations are natural, one is extinct and four have been introduced. In Ireland, of the 74 known populations, approximately 30% are extinct. There is no evidence to indicate that introduced stocks (some of them from Iceland) in a small number of lakes have survived there. A range of factors is involved in the extinction of populations and these include pollution, eutrophication, acidification, afforestation, engineering, exploitation, aquaculture, introductions and climate change. Much research remains to be done and unique stocks of this valuable species will continue to be lost unless positive action is taken through local conservation management backed by appropriate national legislation