Consequences of Electromagnetic Stimulation on Hydraulic Conductivity of Soils

Hydraulic conductivity is a measure of the rate at which water flows through porous media. Because of the dipole properties of water molecules, any electric field can affect hydraulic conductivity. In this study, the effect of radio-frequency (RF) waves on hydraulic conductivity is investigated. This is important both for the geophysical measurement of hydraulic conductivity as well as remediation using electromagnetic waves. Bentonite clay and sandy samples are tested in rigid-wall, cylindrical permeameters and stimulated using a CPVC-cased monopole antenna vertically centered in the permeameters. The permeameters are encased within RF cavities constructed of aluminum mesh in order to prevent interference from outside and to confine the RF wave to the medium. Falling-head and constant-head tests are performed to measure the hydraulic conductivity of the clayey and sandy soil samples, respectively. The results show a correlation between the change in the hydraulic conductivity and the characteristics of the RF stimulation. The change is, however, different for sandy and clayey soils

Results from a set of three-dimensional numerical experiments of a hot Jupiter atmosphere

We present highlights from a large set of simulations of a hot Jupiter atmosphere, nominally based on HD 209458b, aimed at exploring both the evolution of the deep atmosphere, and the acceleration of the zonal flow or jet. We find the occurrence of a super-rotating equatorial jet is robust to changes in various parameters, and over long timescales, even in the absence of strong inner or bottom boundary drag. This jet is diminished in one simulation only, where we strongly force the deep atmosphere equator-to-pole temperature gradient over long timescales. Finally, although the eddy momentum fluxes in our atmosphere show similarities with the proposed mechanism for accelerating jets on tidally-locked planets, the picture appears more complex. We present tentative evidence for a jet driven by a combination of eddy momentum transport and mean flow.Comment: 26 pages, 22 Figures. Accepted for publication in Astronomy and Astrophysic

Large eddy simulation of two-dimensional isotropic turbulence

Large eddy simulation (LES) of forced, homogeneous, isotropic, two-dimensional (2D) turbulence in the energy transfer subrange is the subject of this paper. A difficulty specific to this LES and its subgrid scale (SGS) representation is in that the energy source resides in high wave number modes excluded in simulations. Therefore, the SGS scheme in this case should assume the function of the energy source. In addition, the controversial requirements to ensure direct enstrophy transfer and inverse energy transfer make the conventional scheme of positive and dissipative eddy viscosity inapplicable to 2D turbulence. It is shown that these requirements can be reconciled by utilizing a two-parametric viscosity introduced by Kraichnan (1976) that accounts for the energy and enstrophy exchange between the resolved and subgrid scale modes in a way consistent with the dynamics of 2D turbulence; it is negative on large scales, positive on small scales and complies with the basic conservation laws for energy and enstrophy. Different implementations of the two-parametric viscosity for LES of 2D turbulence were considered. It was found that if kept constant, this viscosity results in unstable numerical scheme. Therefore, another scheme was advanced in which the two-parametric viscosity depends on the flow field. In addition, to extend simulations beyond the limits imposed by the finiteness of computational domain, a large scale drag was introduced. The resulting LES exhibited remarkable and fast convergence to the solution obtained in the preceding direct numerical simulations (DNS) by Chekhlov et al. (1994) while the flow parameters were in good agreement with their DNS counterparts. Also, good agreement with the Kolmogorov theory was found. This LES could be continued virtually indefinitely. Then, a simplifiedComment: 34 pages plain tex + 18 postscript figures separately, uses auxilary djnlx.tex fil

Toroidal versus poloidal magnetic fields in Sun-like stars: a rotation threshold

From a set of stellar spectropolarimetric observations, we report the detection of surface magnetic fields in a sample of four solar-type stars, namely HD 73350, HD 76151, HD 146233 (18 Sco) and HD 190771. Assuming that the observed variability of polarimetric signal is controlled by stellar rotation, we establish the rotation periods of our targets, with values ranging from 8.8 d (for HD 190771) to 22.7 d (for HD 146233). Apart from rotation, fundamental parameters of the selected objects are very close to the Sun's, making this sample a practical basis to investigate the specific impact of rotation on magnetic properties of Sun-like stars. We reconstruct the large-scale magnetic geometry of the targets as a low-order (l<10) spherical harmonics expansion of the surface magnetic field. From the set of magnetic maps, we draw two main conclusions. (a) The magnetic energy of the large-scale field increases with rotation rate. The increase of chromospheric emission with the mean magnetic field is flatter than observed in the Sun. Since the chromospheric flux is also sensitive to magnetic elements smaller than those contributing to the polarimetric signal, this observation suggests that a larger fraction of the surface magnetic energy is stored in large scales as rotation increases. (b) Whereas the magnetic field is mostly poloidal for low rotation rates, more rapid rotators host a large-scale toroidal component in their surface field. From our observations, we infer that a rotation period lower than ~12 days is necessary for the toroidal magnetic energy to dominate over the poloidal component.Comment: MNRAS (in press

The geography of recent genetic ancestry across Europe

The recent genealogical history of human populations is a complex mosaic formed by individual migration, large-scale population movements, and other demographic events. Population genomics datasets can provide a window into this recent history, as rare traces of recent shared genetic ancestry are detectable due to long segments of shared genomic material. We make use of genomic data for 2,257 Europeans (the POPRES dataset) to conduct one of the first surveys of recent genealogical ancestry over the past three thousand years at a continental scale. We detected 1.9 million shared genomic segments, and used the lengths of these to infer the distribution of shared ancestors across time and geography. We find that a pair of modern Europeans living in neighboring populations share around 10-50 genetic common ancestors from the last 1500 years, and upwards of 500 genetic ancestors from the previous 1000 years. These numbers drop off exponentially with geographic distance, but since genetic ancestry is rare, individuals from opposite ends of Europe are still expected to share millions of common genealogical ancestors over the last 1000 years. There is substantial regional variation in the number of shared genetic ancestors: especially high numbers of common ancestors between many eastern populations likely date to the Slavic and/or Hunnic expansions, while much lower levels of common ancestry in the Italian and Iberian peninsulas may indicate weaker demographic effects of Germanic expansions into these areas and/or more stably structured populations. Recent shared ancestry in modern Europeans is ubiquitous, and clearly shows the impact of both small-scale migration and large historical events. Population genomic datasets have considerable power to uncover recent demographic history, and will allow a much fuller picture of the close genealogical kinship of individuals across the world.Comment: Full size figures available from http://www.eve.ucdavis.edu/~plralph/research.html; or html version at http://ralphlab.usc.edu/ibd/ibd-paper/ibd-writeup.xhtm

The ordinary city trap

The paper is a critique of a critique, it explains why the most salient and influential critiques of the neo-Marxist world city and global city concepts, made by those arguing to further postcolonialize urban studies through such suppositions that all cities are ‘ordinary’, are misguided. First, it is explained how the charges of economism and ethnocentrism against the world city and global city concepts are ignoratio elenchi: they do not even begin to address or critique their neo-Marxist argument that, across the difference and diversity of the world’s cities, a few major cities have the necessary economic specialization and therefore extraordinary function of commanding and controlling neoliberal globalization. Second, the error made by advocates of ordinary cities of supposing that world-systems analysis and the world city concept are forms of developmentalism is understood as the source for a wider postcolonial mistake of conflating the neo-Marxist world city and global city literatures with the very neoliberal practices toward urban development that they have long attempted to disclose and counter. Finally, the charges against the world city and global city concepts as paradigmatic, peripheralizing, and normative are also rebutted, not only to highlight how those critiques are consequentialist and dependent on the respective charges of economism, ethnocentrism, and developmentalism having veracity, but to demonstrate how an acceptance of the ordinary cities argument for an idiographic, provincial, nominalist, and comparative approach to urban studies, as an alternative to the two neo-Marxist concepts, is only to fall into the trap of making the mistake of confusing evidence of absence for absence of evidence

Cholesterol and the risk of grade-specific prostate cancer incidence: evidence from two large prospective cohort studies with up to 37 years' follow up

&lt;b&gt;Background&lt;/b&gt; High cholesterol may be a modifiable risk factor for prostate cancer but results have been inconsistent and subject to potential "reverse causality" where undetected disease modifies cholesterol prior to diagnosis.&lt;p&gt;&lt;/p&gt; &lt;b&gt;Methods&lt;/b&gt; We conducted a prospective cohort study of 12,926 men who were enrolled in the Midspan studies between 1970 and 1976 and followed up to 31st December 2007. We used Cox-Proportional Hazards Models to evaluate the association between baseline plasma cholesterol and Gleason grade-specific prostate cancer incidence. We excluded cancers detected within at least 5 years of cholesterol assay.&lt;p&gt;&lt;/p&gt; &lt;b&gt;Results&lt;/b&gt; 650 men developed prostate cancer in up to 37 years' follow-up. Baseline plasma cholesterol was positively associated with hazard of high grade (Gleason score[greater than or equal to]8) prostate cancer incidence (n=119). The association was greatest among men in the 4th highest quintile for cholesterol, 6.1 to &#60;6.69 mmol/l, Hazard Ratio 2.28, 95% CI 1.27 to 4.10, compared with the baseline of &#60;5.05 mmol/l. This association remained significant after adjustment for body mass index, smoking and socioeconomic status.&lt;p&gt;&lt;/p&gt; &lt;b&gt;Conclusions&lt;/b&gt; Men with higher cholesterol are at greater risk of developing high-grade prostate cancer but not overall risk of prostate cancer. Interventions to minimise metabolic risk factors may have a role in reducing incidence of aggressive prostate cancer

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

Personality is influenced by genetic and environmental factors1 and associated with mental health. However, the underlying genetic determinants are largely unknown. We identified six genetic loci, including five novel loci2,3, significantly associated with personality traits in a meta-analysis of genome-wide association studies (N = 123,132–260,861). Of these genomewide significant loci, extraversion was associated with variants in WSCD2 and near PCDH15, and neuroticism with variants on chromosome 8p23.1 and in L3MBTL2. We performed a principal component analysis to extract major dimensions underlying genetic variations among five personality traits and six psychiatric disorders (N = 5,422–18,759). The first genetic dimension separated personality traits and psychiatric disorders, except that neuroticism and openness to experience were clustered with the disorders. High genetic correlations were found between extraversion and attention-deficit– hyperactivity disorder (ADHD) and between openness and schizophrenia and bipolar disorder. The second genetic dimension was closely aligned with extraversion–introversion and grouped neuroticism with internalizing psychopathology (e.g., depression or anxiety)

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.

Because of the high costs associated with ascertainment of families, most linkage studies of Bipolar I disorder (BPI) have used relatively small samples. Moreover, the genetic information content reported in most studies has been less than 0.6. Although microsatellite markers spaced every 10 cM typically extract most of the genetic information content for larger multiplex families, they can be less informative for smaller pedigrees especially for affected sib pair kindreds. For these reasons we collaborated to pool family resources and carried out higher density genotyping. Approximately 1100 pedigrees of European ancestry were initially selected for study and were genotyped by the Center for Inherited Disease Research using the Illumina Linkage Panel 12 set of 6090 single-nucleotide polymorphisms. Of the ~1100 families, 972 were informative for further analyses, and mean information content was 0.86 after pruning for linkage disequilibrium. The 972 kindreds include 2284 cases of BPI disorder, 498 individuals with bipolar II disorder (BPII) and 702 subjects with recurrent major depression. Three affection status models (ASMs) were considered: ASM1 (BPI and schizoaffective disorder, BP cases (SABP) only), ASM2 (ASM1 cases plus BPII) and ASM3 (ASM2 cases plus recurrent major depression). Both parametric and non-parametric linkage methods were carried out. The strongest findings occurred at 6q21 (non-parametric pairs LOD 3.4 for rs1046943 at 119 cM) and 9q21 (non-parametric pairs logarithm of odds (LOD) 3.4 for rs722642 at 78 cM) using only BPI and schizoaffective (SA), BP cases. Both results met genome-wide significant criteria, although neither was significant after correction for multiple analyses. We also inspected parametric scores for the larger multiplex families to identify possible rare susceptibility loci. In this analysis, we observed 59 parametric LODs of 2 or greater, many of which are likely to be close to maximum possible scores. Although some linkage findings may be false positives, the results could help prioritize the search for rare variants using whole exome or genome sequencing

Genomics of Divergence along a Continuum of Parapatric Population Differentiation

MM received funding from the Max Planck innovation funds for this project. PGDF was supported by a Marie Curie European Reintegration Grant (proposal nr 270891). CE was supported by German Science Foundation grants (DFG, EI 841/4-1 and EI 841/6-1)