138 research outputs found

    Cosmic Star Formation, Reionization, and Constraints on Global Chemical Evolution

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    Motivated by the WMAP results indicating an early epoch of reionization, we consider alternative cosmic star formation models which are capable of reionizing the early intergalactic medium. We develop models which include an early burst of massive stars (with several possible mass ranges) combined with standard star formation. We compute the stellar ionizing flux of photons and we track the nucleosynthetic yields for several elements: D, He4, C, N, O, Si, S, Fe, Zn. We compute the subsequent chemical evolution as a function of redshift, both in the intergalactic medium and in the interstellar medium of forming galaxies, starting with the primordial objects which are responsible for the reionization. We apply constraints from the observed abundances in the Lyman alpha forest and in Damped Lyman alpha clouds in conjunction with the ability of the models to produce the required degree of reionization. We also consider possible constraints associated with the observations of the two extremely metal-poor stars HE 0107-5240 and CS22949-037. We confirm that an early top-heavy stellar component is required, as a standard star formation model is unable to reionize the early Universe and reproduce the abundances of the very metal-poor halo stars. A bimodal (or top-heavy) IMF (40 - 100 M_\odot) is our preferred scenario compared to the extreme mass range (\ga 100 M_\odot) often assumed to be responsible for the early stages of reionization. A mode of even more extreme stellar masses in the range (\ge 270 M_\odot) has also been considered. All massive stars in this mode collapse entirely into black holes, and as a consequence, chemical evolution and reionization are de-correlated. [Abstract abbreviated.]Comment: 45 pages, 18 eps figures, as accepted in Ap

    Measuring trust in vaccination: A systematic review.

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    Vaccine acceptance depends on public trust and confidence in the safety and efficacy of vaccines and immunization, the health system, healthcare professionals and the wider vaccine research community. This systematic review analyses the current breadth and depth of vaccine research literature that explicitly refers to the concept of trust within their stated aims or research questions. After duplicates were removed, 19,643 articles were screened by title and abstract. Of these 2,779 were screened by full text, 35 of which were included in the final analysis. These studies examined a range of trust relationships as they pertain to vaccination, including trust in healthcare professionals, the health system, the government, and friends and family members. Three studies examined generalized trust. Findings indicated that trust is often referred to implicitly (19/35), rather than explicitly examined in the context of a formal definition or discussion of the existing literature on trust in a health context. Within the quantitative research analysed, trust was commonly measured with a single-item measure (9/25). Only two studies used validated multi-item measures of trust. Three studies examined changes in trust, either following an intervention or over the course of a pandemic. The findings of this review indicate a disconnect between the current vaccine hesitancy research and the wider health-related trust literature, a dearth in research on trust in low and middle-income settings, a need for studies on how trust levels change over time and investigations on how resilience to trust-eroding information can be built into a trustworthy health system

    Loss of heterozygosity of TRIM3 in malignant gliomas

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    <p>Abstract</p> <p>Background</p> <p>Malignant gliomas are frequent primary brain tumors associated with poor prognosis and very limited response to conventional chemo- and radio-therapies. Besides sharing common growth features with other types of solid tumors, gliomas are highly invasive into adjacent brain tissue, which renders them particularly aggressive and their surgical resection inefficient. Therefore, insights into glioma formation are of fundamental interest in order to provide novel molecular targets for diagnostic purposes and potential anti-cancer drugs. Human <it>Tripartite motif protein 3 </it>(<it>TRIM3</it>) encodes a structural homolog of <it>Drosophila brain tumor </it>(<it>brat</it>) implicated in progenitor cell proliferation control and cancer stem cell suppression. <it>TRIM3 </it>is located within the loss of allelic heterozygosity (LOH) hotspot of chromosome segment 11p15.5, indicating a potential role in tumor suppression. ...</p> <p>Methods</p> <p>Here we analyze 70 primary human gliomas of all types and grades and report somatic deletion mapping as well as single nucleotide polymorphism analysis together with quantitative real-time PCR of chromosome segment 11p15.5.</p> <p>Results</p> <p>Our analysis identifies LOH in 17 cases (24%) of primary human glioma which defines a common 130 kb-wide interval within the <it>TRIM3 </it>locus as a minimal area of loss. We further detect altered genomic dosage of <it>TRIM3 </it>in two glioma cases with LOH at 11p15.5, indicating homozygous deletions of <it>TRIM3</it>.</p> <p>Conclusion</p> <p>Loss of heterozygosity of chromosome segment 11p15.5 in malignant gliomas suggests <it>TRIM3 </it>as a candidate brain tumor suppressor gene.</p

    Negation and the functional sequence

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    There exists a general restriction on admissible functional sequences which prevents adjacent identical heads. We investigate a particular instantiation of this restriction in the domain of negation. Empirically, it manifests itself as a restriction the stacking of multiple negative morphemes. We propose a principled account of this restriction in terms of the general ban on immediately consecutive identical heads in the functional sequence on the one hand, and the presence of a Neg feature inside negative morphemes on the other hand. The account predicts that the stacking of multiple negative morphemes should be possible provided they are separated by intervening levels of structure. We show that this prediction is borne out
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