45 research outputs found

    Hierarchical Growth and Cosmic Star Formation: Enrichment, Outflows and Supernova Rates

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    The cosmic star formation histories are evaluated for different minimum masses of the initial halo structures, with allowance for realistic gas outflows. With a minimum halo mass of 10^{7} - 10^{8} M_odot and a moderate outflow efficiency, we reproduce both the current baryon fraction and the early chemical enrichment of the IGM. The intensity of the formation rate of ``normal'' stars is also well constrained by the observations: it has to be dominated by star formation in elliptical galaxies, except perhaps at very low redshift. The fraction of baryons in stars is predicted as are also the type Ia and II supernova event rates. Comparison with SN observations in the redshift range z=0-2 allows us to set strong constraints on the time delay of type Ia supernovae (a total delay of \sim 4 Gyr is required to fit the data), the lower end of the mass range of the progenitors (2 - 8 M_odot) and the fraction of white dwarfs that reproduce the type Ia supernova (about 1 per cent). The intensity in the initial starburst of zero metallicity stars below 270 M_\odot must be limited in order to avoid premature overenrichment of the IGM. Only about 10 - 20 % of the metals present in the IGM at z = 0 have been produced by population III stars at very high z. The remaining 80 - 90 % are ejected later by galaxies forming normal stars, with a maximum outflow efficiency occurring at a redshift of about 5. We conclude that 10^{-3} of the mass in baryons must lie in first massive stars in order to produce enough ionizing photons to allow early reionization of the IGM by z \sim 15.Comment: 51 pages, 23 eps figure

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    Article A Genome-wide Functional Screen Shows MAGI-1 Is an L1CAM-Dependent Stabilizer of Apical Junctions in C. elegans

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    Summary Background: In multicellular organisms, cell-cell junctions are involved in many aspects of tissue morphogenesis. a-catenin links the cadherin-catenin complex (CCC) to the actin cytoskeleton, stabilizing cadherin-dependent adhesions. Results: To identify modulators of cadherin-based cell adhesion, we conducted a genome-wide RNAi screen in C. elegans and uncovered MAGI-1, a highly conserved protein scaffold. Loss of magi-1 function in wild-type embryos results in disorganized epithelial migration and occasional morphogenetic failure. MAGI-1 physically interacts with the putative actin regulator AFD-1/afadin; knocking down magi-1 or afd-1 function in a hypomorphic a-catenin background leads to complete morphogenetic failure and actin disorganization in the embryonic epidermis. MAGI-1 and AFD-1 localize to a unique domain in the apical junction and normal accumulation of MAGI-1 at junctions requires SAX-7/L1CAM, which can bind MAGI-1 via its C terminus. Depletion of MAGI-1 leads to loss of spatial segregation and expansion of apical junctional domains and greater mobility of junctional proteins. Conclusions: Our screen is the first genome-wide approach to identify proteins that function synergistically with the CCC during epidermal morphogenesis in a living embryo. We demonstrate novel physical interactions between MAGI-1, AFD-1/afadin, and SAX-7/L1CAM, which are part of a functional interactome that includes components of the core CCC. Our results further suggest that MAGI-1 helps to partition and maintain a stable, spatially ordered apical junction during morphogenesis

    Reconfiguration of a Multi-oscillator Network by Light in the Drosophila Circadian Clock

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    The brain clock that drives circadian rhythms of locomotor activity relies on a multi-oscillator neuronal network. In addition to synchronizing the clock with day-night cycles, light also reformats the clock-driven daily activity pattern. How changes in lighting conditions modify the contribution of the different oscillators to remodel the daily activity pattern remains largely unknown. Our data in Drosophila indicate that light readjusts the interactions between oscillators through two different modes. We show that a morning s-LNv \u3e DN1p circuit works in series, whereas two parallel evening circuits are contributed by LNds and other DN1ps. Based on the photic context, the master pacemaker in the s-LNv neurons swaps its enslaved partner-oscillator-LNd in the presence of light or DN1p in the absence of light-to always link up with the most influential phase-determining oscillator. When exposure to light further increases, the light-activated LNd pacemaker becomes independent by decoupling from the s-LNvs. The calibration of coupling by light is layered on a clock-independent network interaction wherein light upregulates the expression of the PDF neuropeptide in the s-LNvs, which inhibits the behavioral output of the DN1p evening oscillator. Thus, light modifies inter-oscillator coupling and clock-independent output-gating to achieve flexibility in the network. It is likely that the light-induced changes in the Drosophila brain circadian network could reveal general principles of adapting to varying environmental cues in any neuronal multi-oscillator system
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