Multi-object spectroscopy of low redshift EIS clusters. I

We report the results of the first multi-object spectroscopic observations at the Danish 1.54m telescope at La Silla, Chile. Observations of five cluster candidates from the ESO Imaging Survey Cluster Candidate Catalog are described. From these observations we confirm the reality of the five clusters with measured redshifts of 0.11<=z<=0.35. We estimate velocity dispersions in the range 294-621km/s indicating rather poor clusters. This, and the measured cluster redshifts are consistent with the results of the matched filter procedure applied to produce the Cluster Candidate Catalog.Comment: 7pages, accepted by Astronomy and Astrophysic

Multi-object spectroscopy of low-redshift EIS clusters IV. Reliability of matched-filter results at z~0.3-0.4

abridged) In this paper we present new redshifts for 747 galaxies in 23 ESO Imaging Survey (EIS) cluster fields. We use the "gap"-technique to search for significant overdensities in redshift space for identifying groups/clusters of galaxies. In this way we spectroscopically confirm systems in 10 of the 23 cluster candidate fields with a matched-filter estimated redshift z_MF=0.3-0.4 and with spectroscopic redshifts in the range from z=0.158 to z=0.534. We find that the systems identified in the present paper span a broad range of one-dimensional velocity dispersion (175-497 km/s) and richness (12L*<=L<=65L*). Both undersampling and contamination by substructures contribute to the uncertainty of these measurements. From the analysis of the colours of the galaxy populations we find that ~60% of the spectroscopically confirmed systems have a "significant" red sequence with a colour matching passive stellar evolution models. With this paper we complete our spectroscopic survey of the fields of 58 EIS cluster candidates with estimated redshifts z<=0.4. We have measured a total of 1954 galaxy redshifts in the range z=0.0065 to z=0.6706. Of the 58 systems we confirm 42 (~75%) with redshifts between z=0.095 and z=0.534.Comment: Accepted for publication in A&A, 19 pages, 11 figure

Intersection local times of independent fractional Brownian motions as generalized white noise functionals

In this work we present expansions of intersection local times of fractional Brownian motions in $\R^d$, for any dimension $d\geq 1$, with arbitrary Hurst coefficients in $(0,1)^d$. The expansions are in terms of Wick powers of white noises (corresponding to multiple Wiener integrals), being well-defined in the sense of generalized white noise functionals. As an application of our approach, a sufficient condition on $d$ for the existence of intersection local times in $L^2$ is derived, extending the results of D. Nualart and S. Ortiz-Latorre in "Intersection Local Time for Two Independent Fractional Brownian Motions" (J. Theoret. Probab.,20(4)(2007), 759-767) to different and more general Hurst coefficients.Comment: 28 page

Multi-object spectroscopy of low redshift EIS clusters. III. Properties of optically selected clusters

We have carried out an investigation of the properties of low redshift EIS clusters using both spectroscopy and imaging data. We present new redshifts for 738 galaxies in 21 ESO Imaging Survey (EIS) Cluster fields. We use the ``gap''-technique to search for significant overdensities in redshift space and to identify groups/clusters of galaxies corresponding to the original EIS matched filter cluster candidates. In this way we spectroscopically confirm 20 of the 21 cluster candidates with a matched-filter estimated redshift z_MF=0.2. We have now obtained spectroscopic redshifts for 34 EIS cluster candidates with z_MF=0.2 (see also Hansen et al., 2002; Olsen et al., 2003). Of those we spectroscopically confirm 32 with redshifts ranging from z=0.064 to 0.283. We find that: 1) the velocity dispersions of the systems range from sigma_v<=130km/s to sigma_v=1200km/s, typical of galaxy groups to rich clusters; 2) richnesses corresponding to Abell classes R<=1; and 3) concentration indices ranging from C=0.2 to C=1.2. From the analysis of the colours of the galaxy populations we find that 53% of the spectroscopically confirmed systems have a ``significant'' red sequence. These systems are on average richer and have higher velocity dispersions. We find that the colour of the red sequence galaxies matches passive stellar evolution predictions.Comment: 24 pages, accepted for publication in A&

Evolution in the Cluster Early-type Galaxy Size-Surface Brightness Relation at z =~ 1

We investigate the evolution in the distribution of surface brightness, as a function of size, for elliptical and S0 galaxies in the two clusters RDCS J1252.9-2927, z=1.237 and RX J0152.7-1357, z=0.837. We use multi-color imaging with the Advanced Camera for Surveys on the Hubble Space Telescope to determine these sizes and surface brightnesses. Using three different estimates of the surface brightnesses, we find that we reliably estimate the surface brightness for the galaxies in our sample with a scatter of < 0.2 mag and with systematic shifts of \lesssim 0.05 mag. We construct samples of galaxies with early-type morphologies in both clusters. For each cluster, we use a magnitude limit in a band which closely corresponds to the rest-frame B, to magnitude limit of M_B = -18.8 at z=0, and select only those galaxies within the color-magnitude sequence of the cluster or by using our spectroscopic redshifts. We measure evolution in the rest-frame B surface brightness, and find -1.41 \+/- 0.14 mag from the Coma cluster of galaxies for RDCS J1252.9-2927 and -0.90 \+/- 0.12 mag of evolution for RX J0152.7-1357, or an average evolution of (-1.13 \+/- 0.15) z mag. Our statistical errors are dominated by the observed scatter in the size-surface brightness relation, sigma = 0.42 \+/- 0.05 mag for RX J0152.7-1357 and sigma = 0.76 \+/- 0.10 mag for RDCS J1252.9-2927. We find no statistically significant evolution in this scatter, though an increase in the scatter could be expected. Overall, the pace of luminosity evolution we measure agrees with that of the Fundamental Plane of early-type galaxies, implying that the majority of massive early-type galaxies observed at z =~ 1 formed at high redshifts.Comment: Accepted in ApJ, 16 pages in emulateapj format with 15 eps figures, 6 in colo

Measuring the impact of health policies using Internet search patterns: the case of abortion

<p>Abstract</p> <p>Background</p> <p>Internet search patterns have emerged as a novel data source for monitoring infectious disease trends. We propose that these data can also be used more broadly to study the impact of health policies across different regions in a more efficient and timely manner.</p> <p>Methods</p> <p>As a test use case, we studied the relationships between abortion-related search volume, local abortion rates, and local abortion policies available for study.</p> <p>Results</p> <p>Our initial integrative analysis found that, both in the US and internationally, the volume of Internet searches for abortion is inversely proportional to local abortion rates and directly proportional to local restrictions on abortion.</p> <p>Conclusion</p> <p>These findings are consistent with published evidence that local restrictions on abortion lead individuals to seek abortion services outside of their area. Further validation of these methods has the potential to produce a timely, complementary data source for studying the effects of health policies.</p

Photo-antagonism of the GABAA receptor

Neurotransmitter receptor trafficking is fundamentally important for synaptic transmission and neural network activity. GABAA receptors and inhibitory synapses are vital components of brain function, yet much of our knowledge regarding receptor mobility and function at inhibitory synapses is derived indirectly from using recombinant receptors, antibody-tagged native receptors and pharmacological treatments. Here we describe the use of a set of research tools that can irreversibly bind to and affect the function of recombinant and neuronal GABAA receptors following ultraviolet photoactivation. These compounds are based on the competitive antagonist gabazine and incorporate a variety of photoactive groups. By using site-directed mutagenesis and ligand-docking studies, they reveal new areas of the GABA binding site at the interface between receptor β and α subunits. These compounds enable the selected inactivation of native GABAA receptor populations providing new insight into the function of inhibitory synapses and extrasynaptic receptors in controlling neuronal excitation

Horizontal DNA transfer mechanisms of bacteria as weapons of intragenomic conflict

Horizontal DNA transfer (HDT) is a pervasive mechanism of diversification in many microbial species, but its primary evolutionary role remains controversial. Much recent research has emphasised the adaptive benefit of acquiring novel DNA, but here we argue instead that intragenomic conflict provides a coherent framework for understanding the evolutionary origins of HDT. To test this hypothesis, we developed a mathematical model of a clonally descended bacterial population undergoing HDT through transmission of mobile genetic elements (MGEs) and genetic transformation. Including the known bias of transformation toward the acquisition of shorter alleles into the model suggested it could be an effective means of counteracting the spread of MGEs. Both constitutive and transient competence for transformation were found to provide an effective defence against parasitic MGEs; transient competence could also be effective at permitting the selective spread of MGEs conferring a benefit on their host bacterium. The coordination of transient competence with cell-cell killing, observed in multiple species, was found to result in synergistic blocking of MGE transmission through releasing genomic DNA for homologous recombination while simultaneously reducing horizontal MGE spread by lowering the local cell density. To evaluate the feasibility of the functions suggested by the modelling analysis, we analysed genomic data from longitudinal sampling of individuals carrying Streptococcus pneumoniae. This revealed the frequent within-host coexistence of clonally descended cells that differed in their MGE infection status, a necessary condition for the proposed mechanism to operate. Additionally, we found multiple examples of MGEs inhibiting transformation through integrative disruption of genes encoding the competence machinery across many species, providing evidence of an ongoing "arms race." Reduced rates of transformation have also been observed in cells infected by MGEs that reduce the concentration of extracellular DNA through secretion of DNases. Simulations predicted that either mechanism of limiting transformation would benefit individual MGEs, but also that this tactic's effectiveness was limited by competition with other MGEs coinfecting the same cell. A further observed behaviour we hypothesised to reduce elimination by transformation was MGE activation when cells become competent. Our model predicted that this response was effective at counteracting transformation independently of competing MGEs. Therefore, this framework is able to explain both common properties of MGEs, and the seemingly paradoxical bacterial behaviours of transformation and cell-cell killing within clonally related populations, as the consequences of intragenomic conflict between self-replicating chromosomes and parasitic MGEs. The antagonistic nature of the different mechanisms of HDT over short timescales means their contribution to bacterial evolution is likely to be substantially greater than previously appreciated

Q&A: What is human language, when did it evolve and why should we care?

Human language is unique among all forms of animal communication. It is unlikely that any other species, including our close genetic cousins the Neanderthals, ever had language, and so-called sign 'language' in Great Apes is nothing like human language. Language evolution shares many features with biological evolution, and this has made it useful for tracing recent human history and for studying how culture evolves among groups of people with related languages. A case can be made that language has played a more important role in our species' recent (circa last 200,000 years) evolution than have our genes