A Rich Cluster of Galaxies Near the Quasar B2 1335+28 at z=1.1: Color Distribution and Star-Formation Properties

We previously reported a significant clustering of red galaxies (R-K=3.5--6) around the radio-loud quasar B2 1335+28 at z=1.086. In this paper, we establish the existence of a rich cluster at the quasar redshift, and study the properties of the cluster galaxies through further detailed analysis of the photometric data. The color distribution of the galaxies in the cluster is quite broad and the fraction of blue galaxies (\sim 70%) is much larger than in intermediate-redshift clusters. Using evolutionary synthesis models, we show that this color distribution can be explained by galaxies with various amounts of star-formation activity mixed with the old stellar populations. Notably, there are about a dozen galaxies which show very red optical-NIR colors but also show significant UV excess with respect to passive-evolution models. They can be interpreted as old early-type galaxies with a small amount of star formation. The fact that the UV-excess red galaxies are more abundant than the quiescent red ones suggests that a large fraction of old galaxies in this cluster are still forming stars to some extent. However, a sequence of quiescent red galaxies is clearly identified on the R-K versus K color-magnitude (C-M) diagram. The slope and zero point of their C-M relation appear to be consistent with those expected for the precursors of the C-M relation of present-day cluster ellipticals when observed at z=1.1. We estimate the Abell richness class of the cluster to be R \sim 1. New X-ray data presented here place an upper limit of L_x < 2 10^{44} erg s^{-1} for the cluster luminosity. Inspections of the wider optical images reveal some lumpy structure, suggesting that the whole system is still dynamically young.Comment: 54 pages including 13 Postscript figures, 1 jpg figure, and 1 table, uses aasms4.sty and epsf.sty. Accepted for publication in ApJ: Replaced as the older verison was missed to include the figure 2c, 2d, and figure

Notch-Fatigue Properties of Advanced TRIP-Aided Bainitic Ferrite Steels

To develop a transformation-induced plasticity (TRIP)-aided bainitic ferrite steel (TBF steel) with high hardenability for a common rail of the next generation diesel engine, 0.2 pct C-1.5 pct Si-1.5 pct Mn-0.05 pct Nb TBF steels with different contents of Cr, Mo, and Ni were produced. The notch-fatigue strength of the TBF steels was investigated and was related to the microstructural and retained austenite characteristics. If Cr, Mo, and/or Ni were added to the base steel, then the steels achieved extremely higher notch-fatigue limits and lower notch sensitivity than base TBF steel and the conventional structural steels. This was mainly associated with (1) carbide-free and fine bainitic ferrite lath structure matrix without proeutectoid ferrite, (2) a large amount of fine metastable retained austenite, and (3) blocky martensite phase including retained austenite, which may suppress a fatigue crack initiation and propagation.ArticleMETALLURGICAL AND MATERIALS TRANSACTIONS A-PHYSICAL METALLURGY AND MATERIALS SCIENCE. 43A(11):4129-4136 (2012)journal articl

A practical device for pinpoint delivery of molecules into multiple neurons in culture

We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture

Maternal Feeding Controls Fetal Biological Clock

BACKGROUND: It is widely accepted that circadian physiological rhythms of the fetus are affected by oscillators in the maternal brain that are coupled to the environmental light-dark (LD) cycle. METHODOLOGY/PRINCIPAL FINDINGS: To study the link between fetal and maternal biological clocks, we investigated the effects of cycles of maternal food availability on the rhythms of Per1 gene expression in the fetal suprachiasmatic nucleus (SCN) and liver using a transgenic rat model whose tissues express luciferase in vitro. Although the maternal SCN remained phase-locked to the LD cycle, maternal restricted feeding phase-advanced the fetal SCN and liver by 5 and 7 hours respectively within the 22-day pregnancy. CONCLUSIONS/SIGNIFICANCE: Our results demonstrate that maternal feeding entrains the fetal SCN and liver independently of both the maternal SCN and the LD cycle. This indicates that maternal-feeding signals can be more influential for the fetal SCN and particular organ oscillators than hormonal signals controlled by the maternal SCN, suggesting the importance of a regular maternal feeding schedule for appropriate fetal molecular clockwork during pregnancy

Impact of COVID-19 on cardiovascular testing in the United States versus the rest of the world

Objectives: This study sought to quantify and compare the decline in volumes of cardiovascular procedures between the United States and non-US institutions during the early phase of the coronavirus disease-2019 (COVID-19) pandemic. Background: The COVID-19 pandemic has disrupted the care of many non-COVID-19 illnesses. Reductions in diagnostic cardiovascular testing around the world have led to concerns over the implications of reduced testing for cardiovascular disease (CVD) morbidity and mortality. Methods: Data were submitted to the INCAPS-COVID (International Atomic Energy Agency Non-Invasive Cardiology Protocols Study of COVID-19), a multinational registry comprising 909 institutions in 108 countries (including 155 facilities in 40 U.S. states), assessing the impact of the COVID-19 pandemic on volumes of diagnostic cardiovascular procedures. Data were obtained for April 2020 and compared with volumes of baseline procedures from March 2019. We compared laboratory characteristics, practices, and procedure volumes between U.S. and non-U.S. facilities and between U.S. geographic regions and identified factors associated with volume reduction in the United States. Results: Reductions in the volumes of procedures in the United States were similar to those in non-U.S. facilities (68% vs. 63%, respectively; p = 0.237), although U.S. facilities reported greater reductions in invasive coronary angiography (69% vs. 53%, respectively; p < 0.001). Significantly more U.S. facilities reported increased use of telehealth and patient screening measures than non-U.S. facilities, such as temperature checks, symptom screenings, and COVID-19 testing. Reductions in volumes of procedures differed between U.S. regions, with larger declines observed in the Northeast (76%) and Midwest (74%) than in the South (62%) and West (44%). Prevalence of COVID-19, staff redeployments, outpatient centers, and urban centers were associated with greater reductions in volume in U.S. facilities in a multivariable analysis. Conclusions: We observed marked reductions in U.S. cardiovascular testing in the early phase of the pandemic and significant variability between U.S. regions. The association between reductions of volumes and COVID-19 prevalence in the United States highlighted the need for proactive efforts to maintain access to cardiovascular testing in areas most affected by outbreaks of COVID-19 infection

Carbonyl Reductase 3 (CBR3) Mediates 9-cis-Retinoic Acid-Induced Cytostatis and is a Potential Prognostic Marker for Oral Malignancy

The molecular mechanisms of growth suppression by retinoic acid (RA) were examined. Our results suggest that the cytostatic effects of RA could be mediated by the activation of endogenous CBR3 gene in oral squamous cell carcinomas (OSCCs), and the expression is a potential marker for oral malignancy