126 research outputs found

    A fundamental problem in our understanding of low-mass galaxy evolution

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    Recent studies have found a dramatic difference between the observed number density evolution of low-mass galaxies and that predicted by semi-analytic models. Whilst models accurately reproduce the z= 0 number density, they require that the evolution occurs rapidly at early times, which is incompatible with the strong late evolution found in observational results. We report here the same discrepancy in two state-of-the-art cosmological hydrodynamical simulations, which is evidence that the problem is fundamental. We search for the underlying cause of this problem using two complementary methods. First, we consider a narrow range in stellar mass of log (Mstar/(h−2M_)) = 9–9.5 and look for evidence of a different history of today’s low-mass galaxies in models and observations. We find that the exclusion of satellite galaxies from the analysis brings the median ages and star formation rates of galaxies into reasonable agreement. However, the models yield too few young, strongly star-forming galaxies. Secondly, we construct a toy model to link the observed evolution of specific star formation rates with the evolution of the galaxy stellar mass function. We infer from this model that a key problem in both semi-analytic and hydrodynamical models is the presence of a positive instead of a negative correlation between specific star formation rate and stellar mass. A similar positive correlation is found between the specific dark matter halo accretion rate and the halo mass, indicating that model galaxies are growing in a way that follows the growth of their host haloes too closely. It therefore appears necessary to find a mechanism that decouples the growth of low-mass galaxies, which occurs primarily at late times, from the growth of their host haloes, which occurs primarily at early times. We argue that the current form of star formation-driven feedback implemented in most galaxy formation models is unlikely to achieve this goal, owing to its fundamental dependence on host halo mass and time

    The dependence of low redshift galaxy properties on environment

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    We review recent results on the dependence of various galaxy properties on environment at low redshift. As environmental indicators, we use group mass, group-centric radius, and the distinction between centrals and satellites; examined galaxy properties include star formation rate, colour, AGN fraction, age, metallicity and concentration. In general, satellite galaxies diverge more markedly from their central counterparts if they reside in more massive haloes. We show that these results are consistent with starvation being the main environmental effect, if one takes into account that satellites that reside in more massive haloes and at smaller halo-centric radii on average have been accreted a longer time ago. Nevertheless, environmental effects are not fully understood yet. In particular, it is puzzling that the impact of environment on a galaxy seems independent of its stellar mass. This may indicate that the stripping of the extended gas reservoir of satellite galaxies predominantly occurs via tidal forces rather than ram-pressure.Comment: Invited Review given at the Workshop "Environment and the Formation of Galaxies: 30 years later" held in Lisbon, 6-7 September 2010. 10 pages, 5 figure

    Gravity at Work: How the Build-Up of Environments Shape Galaxy Properties

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    We present results on the heating of the inter-cluster medium (ICM) by gravitational potential energy from in-falling satellites. We calculate the available excess energy of baryons once they are stripped from their satellite and added to the ICM of the hosting environment. this excess energy is a strong function of environment and we find that it can exceed the contribution from AGNs or supernovae (SN) by up to two orders of magnitude in the densest environments/haloes. Cooling by radiative losses is in general fully compensated by gravitational heating in massive groups and clusters with hot gas temperature > 1 keV. The reason for the strong environment dependence is the continued infall of substructure onto dense environments during their formation in contrast to field-like environments. We show that gravitational heating is able to reduce the number of too luminous galaxies in models and to produce model luminosity functions in agreement with observations.Comment: 8 pages, 3 figures. To be published in Proceedings of JENAM 2010, Symposium 2: "Environment and the formation of galaxies: 30 years later

    An approach to measure compliance to clinical guidelines in psychiatric care

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    <p>Abstract</p> <p>Background</p> <p>The aim of this study was to measure six months compliance to Swedish clinical guidelines in psychiatric care after an active supported implementation process, using structured measures derived from the guidelines.</p> <p>Methods</p> <p>In this observational study four psychiatric clinics each participated in active implementation of the clinical guidelines for the assessment and treatment of depression and guidelines for assessment and treatment of patients with suicidal behaviours developed by The Stockholm Medical Advisory Board for Psychiatry. The implementation programme included seminars, local implementation teams, regular feedback and academic visits. Additionally two clinics only received the guidelines and served as controls. Compliance to guidelines was measured using indicators, which operationalised requirements of preferred clinical practice. 725 patient records were included, 365 before the implementation and 360 six months after.</p> <p>Results</p> <p>Analyses of indicators registered showed that the actively implementing clinics significantly improved their compliance to the guidelines. The total score differed significantly between implementation clinics and control clinics for management of depression (mean scores 9.5 (1.3) versus 5.0 (1.5), p < 0.001) as well as for the management of suicide (mean scores 8.1 (2.3) versus 4.5 (1.9), p < 0.001). No changes were found in the control clinics and only one of the OR was significant.</p> <p>Conclusion</p> <p>Compliance to clinical guidelines measured by process indicators of required clinical practice was enhanced by an active implementation.</p

    Quality assurance in psychiatry: quality indicators and guideline implementation

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    In many occasions, routine mental health care does not correspond to the standards that the medical profession itself puts forward. Hope exists to improve the outcome of severe mental illness by improving the quality of mental health care and by implementing evidence-based consensus guidelines. Adherence to guideline recommendations should reduce costly complications and unnecessary procedures. To measure the quality of mental health care and disease outcome reliably and validly, quality indicators have to be available. These indicators of process and outcome quality should be easily measurable with routine data, should have a strong evidence base, and should be able to describe quality aspects across all sectors over the whole disease course. Measurement-based quality improvement will not be successful when it results in overwhelming documentation reducing the time for clinicians for active treatment interventions. To overcome difficulties in the implementation guidelines and to reduce guideline non-adherence, guideline implementation and quality assurance should be embedded in a complex programme consisting of multifaceted interventions using specific psychological methods for implementation, consultation by experts, and reimbursement of documentation efforts. There are a number of challenges to select appropriate quality indicators in order to allow a fair comparison across different approaches of care. Carefully used, the use of quality indicators and improved guideline adherence can address suboptimal clinical outcomes, reduce practice variations, and narrow the gap between optimal and routine care

    Micro-CT Based Experimental Liver Imaging Using a Nanoparticulate Contrast Agent: A Longitudinal Study in Mice

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    BACKGROUND: Micro-CT imaging of liver disease in mice relies on high soft tissue contrast to detect small lesions like liver metastases. Purpose of this study was to characterize the localization and time course of contrast enhancement of a nanoparticular alkaline earth metal-based contrast agent (VISCOVER ExiTron nano) developed for small animal liver CT imaging. METHODOLOGY: ExiTron nano 6000 and ExiTron nano 12000, formulated for liver/spleen imaging and angiography, respectively, were intravenously injected in C57BL/6J-mice. The distribution and time course of contrast enhancement were analysed by repeated micro-CT up to 6 months. Finally, mice developing liver metastases after intrasplenic injection of colon carcinoma cells underwent longitudinal micro-CT imaging after a single injection of ExiTron nano. PRINCIPAL FINDINGS: After a single injection of ExiTron nano the contrast of liver and spleen peaked after 4-8 hours, lasted up to several months and was tolerated well by all mice. In addition, strong contrast enhancement of abdominal and mediastinal lymph nodes and the adrenal glands was observed. Within the first two hours after injection, particularly ExiTron nano 12000 provided pronounced contrast for imaging of vascular structures. ExiTron nano facilitated detection of liver metastases and provided sufficient contrast for longitudinal observation of tumor development over weeks. CONCLUSIONS: The nanoparticulate contrast agents ExiTron nano 6000 and 12000 provide strong contrast of the liver, spleen, lymph nodes and adrenal glands up to weeks, hereby allowing longitudinal monitoring of pathological processes of these organs in small animals, with ExiTron nano 12000 being particularly optimized for angiography due to its very high initial vessel contrast

    A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumption

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    Mammalian oocytes are arrested at prophase I of meiosis, and resume meiosis prior to ovulation. Coordination of meiotic arrest and resumption is partly dependent on the post-transcriptional regulation of maternal transcripts. Here, we report that, SPINDLIN1 (SPIN1), a maternal protein containing Tudor-like domains, interacts with a known mRNA-binding protein SERBP1, and is involved in regulating maternal transcripts to control meiotic resumption. Mouse oocytes deficient for Spin1 undergo normal folliculogenesis, but are defective in resuming meiosis. SPIN1, via its Tudor-like domain, forms a ribonucleoprotein complex with SERBP1, and regulating mRNA stability and/or translation. The mRNA for the cAMP-degrading enzyme, PDE3A, is reduced in Spin1 mutant oocytes, possibly contributing to meiotic arrest. Our study demonstrates that Spin1 regulates maternal transcripts post-transcriptionally and is involved in meiotic resumption.Ting Gang Chew, Anne Peaston, Ai Khim Lim, Chanchao Lorthongpanich, Barbara B. Knowles, Davor Solte

    Properties of galaxies reproduced by a hydrodynamic simulation.

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    Previous simulations of the growth of cosmic structures have broadly reproduced the 'cosmic web' of galaxies that we see in the Universe, but failed to create a mixed population of elliptical and spiral galaxies, because of numerical inaccuracies and incomplete physical models. Moreover, they were unable to track the small-scale evolution of gas and stars to the present epoch within a representative portion of the Universe. Here we report a simulation that starts 12 million years after the Big Bang, and traces 13 billion years of cosmic evolution with 12 billion resolution elements in a cube of 106.5 megaparsecs a side. It yields a reasonable population of ellipticals and spirals, reproduces the observed distribution of galaxies in clusters and characteristics of hydrogen on large scales, and at the same time matches the 'metal' and hydrogen content of galaxies on small scales

    Genes targeted by the estrogen and progesterone receptors in the human endometrial cell lines HEC1A and RL95-2

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    <p>Abstract</p> <p>Background</p> <p>When the steroid hormones estrogen and progesterone bind to nuclear receptors, they have transcriptional impact on target genes in the human endometrium. These transcriptional changes have a critical function in preparing the endometrium for embryo implantation.</p> <p>Methods</p> <p>382 genes were selected, differentially expressed in the receptive endometrium, to study their responsiveness of estrogen and progesterone. The endometrial cell lines HEC1A and RL95-2 were used as experimental models for the non-receptive and receptive endometrium, respectively. Putative targets for activated steroid hormone receptors were investigated by chromatin immunoprecipitation (ChIP) using receptor-specific antibodies. Promoter occupancy of the selected genes by steroid receptors was detected in ChIP-purified DNA by quantitative PCR (qPCR). Expression analysis by reverse transcriptase (RT)-PCR was used to further investigate hormone dependent mRNA expression regulation of a subset of genes.</p> <p>Results</p> <p>ChIP-qPCR analysis demonstrated that each steroid hormone receptor had distinct group of target genes in the endometrial cell lines. After estradiol treatment, expression of estrogen receptor target genes predominated in HEC1A cells (n = 137) compared to RL95-2 cells (n = 35). In contrast, expression of progesterone receptor target genes was higher in RL95-2 cells (n = 83) than in HEC1A cells (n = 7) after progesterone treatment. RT-PCR analysis of 20 genes demonstrated transcriptional changes after estradiol or progesterone treatment of the cell lines.</p> <p>Conclusions</p> <p>Combined results from ChIP-qPCR and RT-PCR analysis showed different patterns of steroid hormone receptor occupancy at target genes, corresponding to activation or suppression of gene expression after hormone treatment of HEC1A and RL95-2 cell lines.</p
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