421 research outputs found
Substrate Effect on the High Temperature Oxidation Behavior of a Pt-modified Aluminide Coating. Part II: Long-term Cyclic-oxidation Tests at 1,050 C
This second part of a two-part study is devoted to the effect of the substrate on the long-term, cyclic-oxidation behavior at 1,050 C of RT22 industrial coating deposited on three Ni-base superalloys (CMSX-4, SCB, and IN792). Cyclicoxidation tests at 1,050 C were performed for up to 58 cycles of 300 h (i.e., 17,400 h of heating at 1,050 C). For such test conditions, interdiffusion between the coating and its substrate plays a larger role in the damage process of the system than during isothermal tests at 900, 1,050, and 1,150 C for 100 h and cyclicoxidation tests at 900 C which were reported in part I [N. Vialas and D. Monceau,
Oxidation of Metals 66, 155 (2006)]. The results reported in the present paper show that interdiffusion has an important effect on long-term, cyclic-oxidation resistance, so that clear differences can be observed between different superalloys protected with the same aluminide coating. Net-mass-change (NMC) curves show the better cyclic-oxidation behavior of the RT22/IN792 system whereas uncoated CMSX-4 has the best cyclic-oxidation resistance among the three superalloys studied. The importance of the interactions between the superalloy substrate and its coating is then demonstrated. The effect of the substrate on cyclic-oxidation behavior is related to the extent of oxide scale spalling and to the evolution of microstructural
features of the coatings tested. SEM examinations of coating surfaces and cross sections show that spalling on RT22/CMSX-4 and RT22/SCB was favored by the presence of deep voids localized at the coating/oxide interface. Some of these voids can act as nucleation sites for scale spallation. The formation of such interfacial
voids was always observed when the b to c0 transformation leads to the formation of a two-phase b/c0 layer in contact with the alumina scale. On the contrary, no voids
were observed in RT22/IN792, since this b to c0 transformation occurs gradually by an inward transformation of b leading to the formation of a continuous layer of c0
phase, parallel to the metal/scale interface
H_2 emission arises outside photodissociation regions in ultra-luminous infrared galaxies
Ultra-luminous infrared galaxies are among the most luminous objects in the
local universe and are thought to be powered by intense star formation. It has
been shown that in these objects the rotational spectral lines of molecular
hydrogen observed at mid-infrared wavelengths are not affected by dust
obscuration, leaving unresolved the source of excitation of this emission. Here
I report an analysis of archival Spitzer Space Telescope data on ultra-luminous
infrared galaxies and demonstrate that star formation regions are buried inside
optically thick clouds of gas and dust, so that dust obscuration affects
star-formation indicators but not molecular hydrogen. I thereby establish that
the emission of H_2 is not co-spatial with the buried starburst activity and
originates outside the obscured regions. This is rather surprising in light of
the standard view that H_2 emission is directly associated with star-formation
activity. Instead, I propose that H_2 emission in these objects traces shocks
in the surrounding material, which are in turn excited by interactions with
nearby galaxies, and that powerful large-scale shocks cooling by means of H_2
emission may be much more common than previously thought. In the early
universe, a boost in H_2 emission by this process may speed up the cooling of
matter as it collapsed to form the first stars and galaxies and would make
these first structures more readily observable.Comment: Main text and supplemental information, 21 pages including 6 figures,
2 table
"'Asianness Under Construction:' The Contours and Negotiation of Panethnic Identity/Culture among Interethnically Married Asian Americans."
Based on life-history interviews of interethnically married U.S.-raised Asians, this article examines
the meaning and dynamics of Asian American interethnic marriages, and what they reveal about
the complex incorporative process of this βin-betweenβ racial minority group into the U.S.. In
particular, this article explores the connection between Asian American interethnic marriage
and pan-Asian consciousness/identity, both in terms of how panethnicity shapes romantic/
marital desires of individuals and how pan-Asian culture and identity is invented and negotiated
in the process of family-making. My findings indicate that while strong pan-Asian consciousness/
identity underlies the connection among intermarried couples, these unions are not simply
a defensive effort to βpreserveβ Asian-ethnic identity and cultur against a society that still
racializes Asian Americans, but a tentative and often unpremeditated effort to navigate a path
toward integration into the society through an ethnically based, albeit hybrid and reconstructed
identity and culture, that helps the respondents retain the integrity of βAsianness.
A high resolution genome-wide scan for significant selective sweeps: an application to pooled sequence data in laying chickens
In most studies aimed at localizing footprints of past selection, outliers at tails of the empirical distribution of a given test statistic are assumed to reflect locus-specific selective forces. Significance cutoffs are subjectively determined, rather than being related to a clear set of hypotheses. Here, we define an empirical p-value for the summary statistic by means of a permutation method that uses the observed SNP structure in the real data. To illustrate the methodology, we applied our approach to a panel of 2.9 million autosomal SNPs identified from re-sequencing a pool of 15 individuals from a brown egg layer line. We scanned the genome for local reductions in heterozygosity, suggestive of selective sweeps. We also employed a modified sliding window approach that accounts for gaps in the sequence and increases scanning resolution by moving the overlapping windows by steps of one SNP only, and suggest to call this a "creeping window" strategy. The approach confirmed selective sweeps in the region of previously described candidate genes, i.e. TSHR, PRL, PRLHR, INSR, LEPR, IGF1, and NRAMP1 when used as positive controls. The genome scan revealed 82 distinct regions with strong evidence of selection (genome-wide p-value<0.001), including genes known to be associated with eggshell structure and immune system such as CALB1 and GAL cluster, respectively. A substantial proportion of signals was found in poor gene content regions including the most extreme signal on chromosome 1. The observation of multiple signals in a highly selected layer line of chicken is consistent with the hypothesis that egg production is a complex trait controlled by many genes
An OBSL1-Cul7Fbxw8 Ubiquitin Ligase Signaling Mechanism Regulates Golgi Morphology and Dendrite Patterning
The elaboration of dendrites in neurons requires secretory trafficking through the Golgi apparatus, but the mechanisms that govern Golgi function in neuronal morphogenesis in the brain have remained largely unexplored. Here, we report that the E3 ubiquitin ligase Cul7Fbxw8 localizes to the Golgi complex in mammalian brain neurons. Inhibition of Cul7Fbxw8 by independent approaches including Fbxw8 knockdown reveals that Cul7Fbxw8 is selectively required for the growth and elaboration of dendrites but not axons in primary neurons and in the developing rat cerebellum in vivo. Inhibition of Cul7Fbxw8 also dramatically impairs the morphology of the Golgi complex, leading to deficient secretory trafficking in neurons. Using an immunoprecipitation/mass spectrometry screening approach, we also uncover the cytoskeletal adaptor protein OBSL1 as a critical regulator of Cul7Fbxw8 in Golgi morphogenesis and dendrite elaboration. OBSL1 forms a physical complex with the scaffold protein Cul7 and thereby localizes Cul7 at the Golgi apparatus. Accordingly, OBSL1 is required for the morphogenesis of the Golgi apparatus and the elaboration of dendrites. Finally, we identify the Golgi protein Grasp65 as a novel and physiologically relevant substrate of Cul7Fbxw8 in the control of Golgi and dendrite morphogenesis in neurons. Collectively, these findings define a novel OBSL1-regulated Cul7Fbxw8 ubiquitin signaling mechanism that orchestrates the morphogenesis of the Golgi apparatus and patterning of dendrites, with fundamental implications for our understanding of brain development
A Large Fraction of Hydrogen-rich Supernova Progenitors Experience Elevated Mass Loss Shortly Prior to Explosion
Spectroscopic detection of narrow emission lines traces the presence of circumstellar mass distributions around massive stars exploding as core-collapse supernovae. Transient emission lines disappearing shortly after the supernova explosion suggest that the material spatial extent is compact and implies an increased mass loss shortly prior to explosion. Here, we present a systematic survey for such transient emission lines (Flash Spectroscopy) among Type II supernovae detected in the first year of the Zwicky Transient Facility survey. We find that at least six out of ten events for which a spectrum was obtained within two days of the estimated explosion time show evidence for such transient flash lines. Our measured flash event fraction (>30% at 95% confidence level) indicates that elevated mass loss is a common process occurring in massive stars that are about to explode as supernovae
The prevalence and influence of circumstellar material around hydrogen-rich supernova progenitors
Narrow transient emission lines (flash-ionization features) in early
supernova (SN) spectra trace the presence of circumstellar material (CSM)
around the massive progenitor stars of core-collapse SNe. The lines disappear
within days after the SN explosion, suggesting that this material is spatially
confined, and originates from enhanced mass loss shortly (months to a few
years) prior to explosion. We performed a systematic survey of H-rich (Type II)
SNe discovered within less than two days from explosion during the first phase
of the Zwicky Transient Facility (ZTF) survey (2018-2020), finding thirty
events for which a first spectrum was obtained within days from
explosion. The measured fraction of events showing flash ionisation features
( at confidence level) confirms that elevated mass loss in
massive stars prior to SN explosion is common. We find that SNe II showing
flash ionisation features are not significantly brighter, nor bluer, nor more
slowly rising than those without. This implies that CSM interaction does not
contribute significantly to their early continuum emission, and that the CSM is
likely optically thin. We measured the persistence duration of flash ionisation
emission and find that most SNe show flash features for days.
Rarer events, with persistence timescales days, are brighter and rise
longer, suggesting these may be intermediate between regular SNe II and
strongly-interacting SNe IIn
Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family
BACKGROUND: Macular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterized by progressive corneal opacity that starts in early childhood and ultimately progresses to blindness in early adulthood. The aim of this study was to identify the cause of MCD in a black South African family with two affected sisters. METHODS: A multigenerational South African Sotho-speaking family with type I MCD was studied using whole exome sequencing. Variant filtering to identify the MCD-causal mutation included the disease inheritance pattern, variant minor allele frequency and potential functional impact. RESULTS: Ophthalmologic evaluation of the cases revealed a typical MCD phenotype and none of the other family members were affected. An average of 127 713 variants per individual was identified following exome sequencing and approximately 1.2Β % were not present in any of the investigated public databases. Variant filtering identified a homozygous E71Q mutation in CHST6, a known MCD-causing gene encoding corneal N-acetyl glucosamine-6-O-sulfotransferase. This E71Q mutation results in a non-conservative amino acid change in a highly conserved functional domain of the human CHST6 that is essential for enzyme activity. CONCLUSION: We identified a novel E71Q mutation in CHST6 as the MCD-causal mutation in a black South African family with type I MCD. This is the first description of MCD in a black Sub-Saharan African family and therefore contributes valuable insights into the genetic aetiology of this disease, while improving genetic counselling for this and potentially other MCD families. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-016-0308-0) contains supplementary material, which is available to authorized users
The Leukemia-Associated Mllt10/Af10-Dot1l Are Tcf4/Ξ²-Catenin Coactivators Essential for Intestinal Homeostasis
The leukemia-associated Mllt10/Af10 and its partner the histone methyltransferase Dot1l are identified as Tcf4/Ξ²-catenin co-activators and shown to be essential for Wnt-driven endogenous gene expression, intestinal development and homeostasis
Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5
Reversible post-translational protein modifications such as SUMOylation add complexity to cardiac transcriptional regulation. The homeodomain transcription factor Nkx2-5/Csx is essential for heart specification and morphogenesis. It has been previously suggested that SUMOylation of lysine 51 (K51) of Nkx2-5 is essential for its DNA binding and transcriptional activation. Here, we confirm that SUMOylation strongly enhances Nkx2-5 transcriptional activity and that residue K51 of Nkx2-5 is a SUMOylation target. However, in a range of cultured cell lines we find that a point mutation of K51 to arginine (K51R) does not affect Nkx2-5 activity or DNA binding, suggesting the existence of additional Nkx2-5 SUMOylated residues. Using biochemical assays, we demonstrate that Nkx2-5 is SUMOylated on at least one additional site, and this is the predominant site in cardiac cells. The second site is either non-canonical or a βshiftingβ site, as mutation of predicted consensus sites and indeed every individual lysine in the context of the K51R mutation failed to impair Nkx2-5 transcriptional synergism with SUMO, or its nuclear localization and DNA binding. We also observe SUMOylation of Nkx2-5 cofactors, which may be critical to Nkx2-5 regulation. Our data reveal highly complex regulatory mechanisms driven by SUMOylation to modulate Nkx2-5 activity
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