843 research outputs found

    Effects of large-scale environment on the assembly history of central galaxies

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    We examine whether large-scale environment affects the mass assembly history of their central galaxies. To facilitate this, we constructed dark matter halo merger trees from a cosmological N-body simulation and calculated the formation and evolution of galaxies using a semi-analytic method. We confirm earlier results that smaller halos show a notable difference in formation time with a mild dependence on large-scale environment. However, using a semi-analytic model, we found that on average the growth rate of the stellar mass of central galaxies is largely insensitive to large-scale environment. Although our results show that the star formation rate (SFR) and the stellar mass of central galaxies in smaller halos are slightly affected by the assembly bias of halos, those galaxies are faint, and the difference in the SFR is minute, and therefore it is challenging to detect it in real galaxies given the current observational accuracy. Future galaxy surveys, such as the BigBOSS experiment and the Large Synoptic Survey Telescope, which are expected to provide observational data for fainter objects, will provide a chance to test our model predictions.Comment: 7 pages, 5 figure

    Merger relics of cluster galaxies

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    Context. Sheen and collaborators recently found that a surprisingly large portion (38%) of massive early-type galaxies in heavy clusters show strong merger-related disturbed features. This contradicts the general understanding that massive clusters are hostile environments for galaxy mergers. Considering the significance of mergers in galaxy evolution, it is important to understand this. Aims. We aim to present a theoretical foundation that explains galaxy mergers in massive clusters. Methods. We used the N-body simulation technique to perform a cosmological-volume simulation and derive dark-halo merger trees. Then, we used the semi-analytic modeling technique to populate each halo with galaxies. We ran hydrodynamic simulations of galaxy mergers to estimate the lifetime of merger features for the imaging condition used by Sheen and collaborators. We applied this merger feature lifetime to our semi-analytic models. Finally, we counted the massive early-type galaxies in heavy model clusters that would show strong merger features. Results. While there still are substantial uncertainties, our preliminary results are remarkably close to the observed fraction of galaxies with merger features. Key ingredients for the success are twofold: firstly, the subhalo motion in dark haloes has been accurately traced, and, second, the lifetime of merger features has been properly estimated. As a result, merger features are expected to last very long in cluster environments. Many massive early-type galaxies in heavy clusters therefore show merger features not because they experience mergers in the current clusters in situ, but because they still carry their merger features from their previous halo environments. Conclusions. Investigating the merger relics of cluster galaxies is potentially important, because it uniquely allows us to backtrack the halo merger history.Comment: 4 pages, 3 figures, accepted for publication in A&A Research Not

    Turning behaviors of T cells climbing up ramp-like structures are regulated by myosin light chain kinase activity and lamellipodia formation

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    T cells navigate diverse microenvironments to perform immune responses. Micro-scale topographical structures within the tissues, which may inherently exist in normal tissues or may be formed by inflammation or injury, can influence T cell migration, but how T cell migration is affected by such topographical structures have not been investigated. In this study, we fabricated ramp-like structures with a 5 mu m height and various slopes, and observed T cells climbing up the ramp-like structures. T cells encountering the ramp-like structures exhibited MLC accumulation near head-tail junctions contacting the ramp-like structures, and made turns to the direction perpendicular to the ramp-like structures. Pharmacological study revealed that lamellipodia formation mediated by arp2/3 and contractility regulated by myosin light chain kinase (MLCK) were responsible for the intriguing turning behavior of T cells climbing the ramp-like structures. Arp2/3 or MLCK inhibition substantially reduced probability of T cells climbing sharp-edged ramp-like structures, indicating intriguing turning behavior of T cells mediated by lamellipodia formation and MLCK activity may be important for T cells to access inflamed or injured tissues with abrupt topographical changes.11Ysciescopu

    Public Finance Responses to COVID-19 in Korea

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    Technical Adequacy of Curriculum-Based Measures in Writing in Grades 1ā€“3

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    The purpose of this study was to investigate evidence of reliability, criterion validity, and grade-level differences of curriculum-based measures of writing (CBM-W) with 612 students in grades 1ā€“3. Four scoring procedures (words written, words spelled correctly, correct word sequences, and correct minus incorrect word sequences) were used with two CBM-W tasks (pictureā€“word and story prompt) during fall, winter, and spring of one academic year. A subsample of participants (nā€‰=ā€‰244) were given a criterion measure in spring of the academic year. Pearsonā€™s r coefficients were calculated to determine evidence of alternate form reliability and criterion validity, and a MANOVA was used to detect significant growth within and across grade levels. Results indicated that scores on both CBM-W tasks had adequate reliability and validity coefficients in grades 2ā€“3 and mixed results in grade 1. Significant growth was detected within and across all grades at each time point on each task. Implications for research and practice are discussed

    X-ray: Discovering DRAM Internal Structure and Error Characteristics by Issuing Memory Commands

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    The demand for accurate information about the internal structure and characteristics of dynamic random-access memory (DRAM) has been on the rise. Recent studies have explored the structure and characteristics of DRAM to improve processing in memory, enhance reliability, and mitigate a vulnerability known as rowhammer. However, DRAM manufacturers only disclose limited information through official documents, making it difficult to find specific information about actual DRAM devices. This paper presents reliable findings on the internal structure and characteristics of DRAM using activate-induced bitflips (AIBs), retention time test, and row-copy operation. While previous studies have attempted to understand the internal behaviors of DRAM devices, they have only shown results without identifying the causes or have analyzed DRAM modules rather than individual chips. We first uncover the size, structure, and operation of DRAM subarrays and verify our findings on the characteristics of DRAM. Then, we correct misunderstood information related to AIBs and demonstrate experimental results supporting the cause of rowhammer. We expect that the information we uncover about the structure, behavior, and characteristics of DRAM will help future DRAM research.Comment: 4 pages, 7 figure

    Rhus verniciflua Stokes against Advanced Cancer: A Perspective from the Korean Integrative Cancer Center

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    Active anticancer molecules have been searched from natural products; many drugs were developed from either natural products or their derivatives following the conventional pharmaceutical paradigm of drug discovery. However, the advances in the knowledge of cancer biology have led to personalized medicine using molecular-targeted agents which create new paradigm. Clinical benefit is dependent on individual biomarker and overall survival is prolonged through cytostatic rather than cytotoxic effects to cancer cell. Therefore, a different approach is needed from the single lead compound screening model based on cytotoxicity. In our experience, the Rhus verniciflua stoke (RVS) extract traditionally used for cancer treatment is beneficial to some advanced cancer patients though it is herbal extract not single compound, and low cytotoxic in vitro. The standardized RVS extract's action mechanisms as well as clinical outcomes are reviewed here. We hope that these preliminary results would stimulate different investigation in natural products from conventional chemicals
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