355 research outputs found
The structure ofAl(111)-K−(√3 × √3)R30° determined by LEED: stable and metastable adsorption sites
It is found that the adsorption of potassium on Al(111) at 90 K and at 300 K both result in a (√3 × √3)R0° structure. Through a detailed LEED analysis it is revealed that at 300 K the adatoms occupy substitutional sites and at 90 K the adatoms occupy on-top sites; both geometries have hitherto been considered as very unusual. The relationship between bond length and coordination is discussed with respect to the present results, and with respect to other quantitative studies of alkali-metal/metal adsorption systems
Spatiotemporal Distribution of Harmful Algal Flora in the Tropical Estuarine Complex of Goa, India
Mandovi and Zuari estuarine complex is monsoon-influenced estuaries located along the central west coast of India. During the past few years, there has been an increase in nutrient loading specially during monsoonal runoff which is responsible for the growth of harmful algal flora. To understand occurrence and distribution of harmful algal blooms species, daily/alternate day samplings were carried out in Mandovi and Zuari estuaries during 2007-2008 and 2008-2009 periods, respectively, comprising of monsoon (June–November) and nonmonsoon (December–May). In Mandovi, total 54 HAB species with 49 in monsoon and 36 during nonmonsoon period were reported. In Zuari, total 46 HAB species with 38 in monsoon and 41 were reported during nonmonsoon period. Bray-Curtis cluster analysis based on log-transformed phytoplankton density detected seven well-defined groups revealing spatiotemporal variability. The density of the dominant harmful algal species was significantly positively correlated with nutrients, but negatively correlated with salinity. The results of the study indicate that monsoon plays an important role in occurrence and distribution of harmful algal species having direct correlation with salinity variations and nutrient loading
Changes in the source and transport mechanism of terrigenous input to the Indian sector of southern ocean during the late quaternary and its palaeoceanographic implications
Changes in the terrigenous sediment source and transport mechanisms during the late Quaternary
have been investigated using four sediment cores within the Indian sector of Southern Ocean,
using the magnetic susceptibility (MS) and sedimentological records. Sediments deposited during
the Holocene and other interglacial periods were characterised by low MS, low sand content,
reduced ice-rafted detritus (IRD) input and increased illite possibly transported via hydrographic
advection from the south. The glacial intervals are characterised by high MS, high sand content,
increased IRD input and reduced illite clays, derived from both local as well as Antarctic sources.
Significant reduction in clay fraction and illite content during glacials suggests that the erosive
and transporting capabilities of the deep and bottom waters could have reduced compared to the
interglacial times. The changes in terrigenous influx to this region were significantly influenced by
the rhythmic glacial–interglacial fluctuations in bottom circulation and the position of the Polar
Front
McSAFE - High performance Monte Carlo methods for SAFEty demonstration, From proof of concept to industry-like applications
Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia
OBJECTIVES:
To prospectively assess the value of serum total bilirubin (TB) within 3 months of hepatoportoenterostomy (HPE) in infants with biliary atresia as a biomarker predictive of clinical sequelae of liver disease in the first 2 years of life.
STUDY DESIGN:
Infants with biliary atresia undergoing HPE between June 2004 and January 2011 were enrolled in a prospective, multicenter study. Complications were monitored until 2 years of age or the earliest of liver transplantation (LT), death, or study withdrawal. TB below 2 mg/dL (34.2 μM) at any time in the first 3 months (TB <2.0, all others TB ≥ 2) after HPE was examined as a biomarker, using Kaplan-Meier survival and logistic regression.
RESULTS:
Fifty percent (68/137) of infants had TB < 2.0 in the first 3 months after HPE. Transplant-free survival at 2 years was significantly higher in the TB < 2.0 group vs TB ≥ 2 (86% vs 20%, P < .0001). Infants with TB ≥ 2 had diminished weight gain (P < .0001), greater probability of developing ascites (OR 6.4, 95% CI 2.9-14.1, P < .0001), hypoalbuminemia (OR 7.6, 95% CI 3.2-17.7, P < .0001), coagulopathy (OR 10.8, 95% CI 3.1-38.2, P = .0002), LT (OR 12.4, 95% CI 5.3-28.7, P < .0001), or LT or death (OR 16.8, 95% CI 7.2-39.2, P < .0001).
CONCLUSIONS:
Infants whose TB does not fall below 2.0 mg/dL within 3 months of HPE were at high risk for early disease progression, suggesting they should be considered for LT in a timely fashion. Interventions increasing the likelihood of achieving TB <2.0 mg/dL within 3 months of HPE may enhance early outcomes
Enhanced surface vibrations and reconstruction of the Al(111) surface induced by Rb adsorption
Recurrence of Primary Sclerosing Cholangitis After Liver Transplant in Children : An International Observational Study
Background and Aims Recurrent primary sclerosing cholangitis (rPSC) following liver transplant (LT) has a negative impact on graft and patient survival; little is known about risk factors for rPSC or disease course in children. Approach and Results We retrospectively evaluated risk factors for rPSC in 140 children from the Pediatric PSC Consortium, a multicenter international registry. Recipients underwent LT for PSC and had >90 days of follow-up. The primary outcome, rPSC, was defined using Graziadei criteria. Median follow-up after LT was 3 years (interquartile range 1.1-6.1). rPSC occurred in 36 children, representing 10% and 27% of the subjects at 2 years and 5 years following LT, respectively. Subjects with rPSC were younger at LT (12.9 vs. 16.2 years), had faster progression from PSC diagnosis to LT (2.5 vs. 4.1 years), and had higher alanine aminotransferase (112 vs. 66 IU/L) at LT (all P < 0.01). Inflammatory bowel disease was more prevalent in the rPSC group (86% vs. 66%; P = 0.025). After LT, rPSC subjects had more episodes of biopsy-proved acute rejection (mean 3 vs. 1; P < 0.001), and higher prevalence of steroid-refractory rejection (41% vs. 20%; P = 0.04). In those with rPSC, 43% developed complications of portal hypertension, were relisted for LT, or died within 2 years of the diagnosis. Mortality was higher in the rPSC group (11.1% vs. 2.9%; P = 0.05). Conclusions The incidence of rPSC in this cohort was higher than previously reported, and was associated with increased morbidity and mortality. Patients with rPSC appeared to have a more aggressive, immune-reactive phenotype. These findings underscore the need to understand the immune mechanisms of rPSC, to lay the foundation for developing new therapies and improve outcomes in this challenging population.Peer reviewe
Targeted calcium influx boosts cytotoxic T lymphocyte function in the tumour microenvironment
Adoptive cell transfer utilizing tumour-targeting cytotoxic T lymphocytes (CTLs) is one of the most effective immunotherapies against haematological malignancies, but significant clinical success has not yet been achieved in solid tumours due in part to the strong immunosuppressive tumour microenvironment. Here, we show that suppression of CTL killing by CD4+CD25+Foxp+ regulatory T cell (Treg) is in part mediated by TGFβ-induced inhibition of inositol trisphosphate (IP3) production, leading to a decrease in T cell receptor (TCR)-dependent intracellular Ca2+ response. Highly selective optical control of Ca2+ signalling in adoptively transferred CTLs enhances T cell activation and IFN-γ production in vitro, leading to a significant reduction in tumour growth in mice. Altogether, our findings indicate that the targeted optogenetic stimulation of intracellular Ca2+ signal allows for the remote control of cytotoxic effector functions of adoptively transferred T cells with outstanding spatial resolution by boosting T cell immune responses at the tumour sites
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