ASASSN-15oi: A Rapidly Evolving, Luminous Tidal Disruption Event at 216 Mpc

We present ground-based and Swift photometric and spectroscopic observations of the tidal disruption event (TDE) ASASSN-15oi, discovered at the center of 2MASX J20390918-3045201 ($d\simeq216$ Mpc) by the All-Sky Automated Survey for SuperNovae (ASAS-SN). The source peaked at a bolometric luminosity of $L\simeq1.9\times10^{44}$ ergs s$^{-1}$ and radiated a total energy of $E\simeq5.0\times10^{50}$ ergs over the $\sim3.5$ months of observations. The early optical/UV emission of the source can be fit by a blackbody with temperature increasing from $T\sim2\times10^4$ K to $T\sim6\times10^4$ K while the luminosity declines from $L\simeq1.9\times10^{44}$ ergs s$^{-1}$ to $L\simeq2.8\times10^{43}$ ergs s$^{-1}$, requiring the photosphere to be shrinking rapidly. The optical/UV luminosity decline is broadly consistent with an exponential decline, $L\propto e^{-t/t_0}$, with $t_0\simeq35$ days. ASASSN-15oi also exhibits roughly constant soft X-ray emission that is significantly weaker than the optical/UV emission. Spectra of the source show broad helium emission lines and strong blue continuum emission in early epochs, although these features fade rapidly and are not present $\sim3$ months after discovery. The early spectroscopic features and color evolution of ASASSN-15oi are consistent with a TDE, but the rapid spectral evolution is unique among optically-selected TDEs

Simplified Rolled Technique at Implantâ Uncovering Surgery for Correcting Horizontal Ridge Defect

Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/142141/1/cap0140.pd

H-ATLAS/GAMA: The nature and characteristics of optically red galaxies detected at submillimetre wavelengths

We combine Herschel/SPIRE sub-millimeter (submm) observations with existing multi-wavelength data to investigate the characteristics of low redshift, optically red galaxies detected in submm bands. We select a sample of galaxies in the redshift range 0.01$\leq$z$\leq$0.2, having >5$\sigma$ detections in the SPIRE 250 micron submm waveband. Sources are then divided into two sub-samples of $red$ and $blue$ galaxies, based on their UV-optical colours. Galaxies in the $red$ sample account for $\approx$4.2 per cent of the total number of sources with stellar masses M$_{*}\gtrsim$10$^{10}$ Solar-mass. Following visual classification of the $red$ galaxies, we find that $\gtrsim$30 per cent of them are early-type galaxies and $\gtrsim$40 per cent are spirals. The colour of the $red$-spiral galaxies could be the result of their highly inclined orientation and/or a strong contribution of the old stellar population. It is found that irrespective of their morphological types, $red$ and $blue$ sources occupy environments with more or less similar densities (i.e., the $\Sigma_5$ parameter). From the analysis of the spectral energy distributions (SEDs) of galaxies in our samples based on MAGPHYS, we find that galaxies in the $red$ sample (of any morphological type) have dust masses similar to those in the $blue$ sample (i.e. normal spiral/star-forming systems). However, in comparison to the $red$-spirals and in particular $blue$ systems, $red$-ellipticals have lower mean dust-to-stellar mass ratios. Besides galaxies in the $red$-elliptical sample have much lower mean star-formation/specific-star-formation rates in contrast to their counterparts in the $blue$ sample. Our results support a scenario where dust in early-type systems is likely to be of an external origin

A versatile method for preparation of hydrated microbial-latex biocatalytic coatings for gas absorption and gas evolution

We describe a latex wet coalescence method for gas-phase immobilization of microorganisms on paper which does not require drying for adhesion. This method reduces drying stresses to the microbes. It is applicable for microorganisms that do not tolerate desiccation stress during latex drying even in the presence of carbohydrates. Small surface area, 10-65 mu m thick coatings were generated on chromatography paper strips and placed in the head-space of vertical sealed tubes containing liquid to hydrate the paper. These gas-phase microbial coatings hydrated by liquid in the paper pore space demonstrated absorption or evolution of H-2, CO, CO2 or O-2. The microbial products produced, ethanol and acetate, diffuse into the hydrated paper pores and accumulate in the liquid at the bottom of the tube. The paper provides hydration to the back side of the coating and also separates the biocatalyst from the products. Coating reactivity was demonstrated for Chlamydomonas reinhardtii CC124, which consumed CO2 and produced 10.2 +/- A 0.2 mmol O-2 m(-2) h(-1), Rhodopseudomonas palustris CGA009, which consumed acetate and produced 0.47 +/- A 0.04 mmol H-2 m(-2) h(-1), Clostridium ljungdahlii OTA1, which consumed 6 mmol CO m(-2) h(-1), and Synechococcus sp. PCC7002, which consumed CO2 and produced 5.00 +/- A 0.25 mmol O-2 m(-2) h(-1). Coating thickness and microstructure were related to microbe size as determined by digital micrometry, profilometry, and confocal microscopy. The immobilization of different microorganisms in thin adhesive films in the gas phase demonstrates the utility of this method for evaluating genetically optimized microorganisms for gas absorption and gas evolution

Identification of intracellular bacteria from multiple single-cell RNA-seq platforms using CSI-Microbes

The study of the tumor microbiome has been garnering increased attention. We developed a computational pipeline (CSI-Microbes) for identifying microbial reads from single-cell RNA sequencing (scRNA-seq) data and for analyzing differential abundance of taxa. Using a series of controlled experiments and analyses, we performed the first systematic evaluation of the efficacy of recovering microbial unique molecular identifiers by multiple scRNA-seq technologies, which identified the newer 10x chemistries (3' v3 and 5') as the best suited approach. We analyzed patient esophageal and colorectal carcinomas and found that reads from distinct genera tend to co-occur in the same host cells, testifying to possible intracellular polymicrobial interactions. Microbial reads are disproportionately abundant within myeloid cells that up-regulate proinflammatory cytokines like IL1Β and CXCL8, while infected tumor cells up-regulate antigen processing and presentation pathways. These results show that myeloid cells with bacteria engulfed are a major source of bacterial RNA within the tumor microenvironment (TME) and may inflame the TME and influence immunotherapy response

Manga 'Ubá' tratada com ethephon na pré-colheita

A manga 'Ubá' amadurece, geralmente, de novembro a janeiro, e a maturação desuniforme em uma mesma planta exige colheita escalonada, que pode prolongar-se por até um mês. Foram avaliados os efeitos de diferentes concentrações de ethephon na antecipação e na uniformização do amadurecimento e nos atributos de qualidade da manga 'Ubá'. Na 17ª semana após a antese, 25 mangueiras, sendo cinco por tratamento, foram pulverizadas com ethephon, nas concentrações de 0, 250, 500, 750 e 1000 mg L-1, acrescido de 0,5% de óleo mineral. Foram colhidos cinco frutos de cada planta, diariamente, até o completo amadurecimento, com exceção da dose 0 mg L-1, em que, a partir de seis dias após aplicação do ethephon (DAAE), a colheita foi semanal, até 41 DAAE. Os frutos colhidos foram armazenados a 20,0 ± 0,8 °C e a 90 ± 5% de umidade relativa e avaliados após o completo amadurecimento. A aplicação do ethephon em pré-colheita antecipou a colheita de manga 'Ubá' em até 36 dias, uniformizou o amadurecimento dos frutos na planta e dispensou a climatização em pós-colheita. Após a aplicação do ethephon, quanto mais tardia a colheita, mais rapidamente completou-se o amadurecimento e melhor foi a qualidade final do fruto. A concentração de 750 mg L-1 de ethephon, seguida da colheita três dias depois, foi a que proporcionou frutos de melhor qualidade

Non-Stationarity in the “Resting Brain’s” Modular Architecture

Task-free functional magnetic resonance imaging (TF-fMRI) has great potential for advancing the understanding and treatment of neurologic illness. However, as with all measures of neural activity, variability is a hallmark of intrinsic connectivity networks (ICNs) identified by TF-fMRI. This variability has hampered efforts to define a robust metric of connectivity suitable as a biomarker for neurologic illness. We hypothesized that some of this variability rather than representing noise in the measurement process, is related to a fundamental feature of connectivity within ICNs, which is their non-stationary nature. To test this hypothesis, we used a large (n = 892) population-based sample of older subjects to construct a well characterized atlas of 68 functional regions, which were categorized based on independent component analysis network of origin, anatomical locations, and a functional meta-analysis. These regions were then used to construct dynamic graphical representations of brain connectivity within a sliding time window for each subject. This allowed us to demonstrate the non-stationary nature of the brain’s modular organization and assign each region to a “meta-modular” group. Using this grouping, we then compared dwell time in strong sub-network configurations of the default mode network (DMN) between 28 subjects with Alzheimer’s dementia and 56 cognitively normal elderly subjects matched 1∶2 on age, gender, and education. We found that differences in connectivity we and others have previously observed in Alzheimer’s disease can be explained by differences in dwell time in DMN sub-network configurations, rather than steady state connectivity magnitude. DMN dwell time in specific modular configurations may also underlie the TF-fMRI findings that have been described in mild cognitive impairment and cognitively normal subjects who are at risk for Alzheimer’s dementia