Multi-messenger observations of a binary neutron star merger

On 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40+8-8 Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 Mo. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One- Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transient’s position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta

Gall-inducing insects from Campos de Altitude, Brazil

Insetos indutores de galhas são muito ricos em espécies nas formações vegetais do sudeste do Brasil. O objetivo deste estudo foi descrever a riqueza de morfotipos de galha por meio da caracterização de suas formas externas e os padrões de ocorrência nas plantas hospedeiras. As amostragens foram realizadas em campos rupestres e altitudinais de quatro regiões da Serra da Mantiqueira: 1) campos de altitude do Parque Estadual do Brigadeiro e 2) Parque Nacional do Caparaó, 3) Parque Estadual do Ibitipoca e Parque Nacional do Itatiaia. Foram registradas 93 espécies de galhas induzidas por insetos em 13 famílias, 30 gêneros e 50 espécies de plantas hospedeiras. Sendo 38 a riqueza de insetos indutores de galhas do Parque Estadual do Brigadeiro, 21 do Parque Nacional do Caparaó, 23 do Parque Nacional do Caparaó e 20 do Parque Nacional do Itatiaia. As famílias com maior riqueza foram Asteraceae (33%) e Melastomataceae (17%). A família Cecydomiidae (Diptera) foi a mais frequente (98%). O órgão mais atacado foi o caule (56%) seguido de folha (23%). O fato de apenas 12% das galhas descritas neste estudo já terem sido registradas em trabalhos anteriores, reforça a necessidade em aumentar o esforço amostral na direção de um maior conhecimento sobre a riqueza e história natural dos insetos indutores de galhas no Brasil. ____________________________________________________________________________________ABSTRACT: Gall-inducing insects are very specious in vegetations of southeastern Brazil. Our goal was describe the gall richness by characterizing their external forms and their patterns of occurrence on host plants. Samples were collected from Campos de Altitude at four regions of the Mantiqueira Range: 1) Parque Estadual da Serra do Brigadeiro, 2) Parque Nacional do Caparaó, 3) Parque Estadual do Ibitipoca, 4) Parque Nacional do Itatiaia. We found 93 gall species within 13 families, 30 genera and 50 host plant species. We recorded 38 gall species in Parque Estadual da Serra do Brigadeiro, 21 in Parque Nacional do Caparaó, 23 in Parque Estadual do Ibitipoca and 20 in Parque Nacional do Itatiaia. Asteraceae represented 33% of the species collected, followed by Melastomataceae at 17%; with each one concentrating 56% and 18% of the galling insects, respectively. 98% of galls were Cecydomiidae (Diptera). The most attacked organ was the stem (56%), followed by the leaf (23%). Only 12% of the galls described in our study had been already recorded in previous studies, thus reinforcing the need to increase the sampling effort toward a better understanding of the richness and the natural history of gall-inducing insects from Brazil

Noncoding RNA transcription targets AID to divergently transcribed loci in B cells

The vast majority of the mammalian genome has the potential to expressnoncoding RNA (ncRNA). The 11-subunit RNA exosome complex is the main source of cellular 3′–5′ exoribonucleolytic activity and potentially regulates the mammalian noncoding transcriptome(1). Here we generated a mouse model in which the essential subunit Exosc3 of the RNA exosome complex can be conditionally deleted. Exosc3-deficient B cells lack the ability to undergo normal levels of class switch recombination and somatic hypermutation, two mutagenic DNA processes used to generate antibody diversity via the B-cell mutator protein activation-induced cytidine deaminase (AID)(2,3). The transcriptome of Exosc3-deficient B cells has revealed the presence of many novel RNA exosome substrate ncRNAs. RNA exosome substrate RNAs include xTSS-RNAs, transcription start site (TSS)-associated antisense transcripts that can exceed 500 base pairs in length and are transcribed divergently from cognate coding gene transcripts. xTSS-RNAs are most strongly expressed at genes that accumulate AID-mediated somatic mutations and/or are frequent translocation partners of DNA double-strand breaks generated at Igh in B cells(4,5). Strikingly, translocations near TSSs or within gene bodies occur over regions of RNA exosome substrate ncRNA expression. These RNA exosome-regulated, antisense-transcribed regions of the B-cell genome recruit AID and accumulate single-strand DNA structures containing RNA–DNA hybrids. We propose that RNA exosome regulation of ncRNA recruits AID to single-strand DNA-forming sites of antisense and divergent transcription in the B-cell genome, thereby creating a link between ncRNA transcription and overall maintenance of B-cell genomic integrity