Brominated flame retardants and natural organobrominated compounds in a vulnerable delphinid species along the Brazilian coast

Guiana dolphins, Sotalia guianensis, are vulnerable to extinction along their distribution on the Brazilian coast and assessing chemical pollution is of utmost importance for their conservation. For this study, 51 carcasses of Guiana dolphins were sampled across the Brazilian coast to investigate legacy and emerging brominated flame retardants (BFRs) as well as the naturally-produced MeO-BDEs. PBDEs and MeO-BDEs were detected in all samples analyzed, whereas emerging BFRs were detected in 16 % of the samples, all in Rio de Janeiro state. PBDE concentrations varied between 2.24 and 799 ng.g-1 lipid weight (lw), emerging BFRs between 0.12 and 1.51 ng.g-1 lw and MeO-BDEs between 3.82 and 10,247 ng.g-1 lw. Concentrations of legacy and emerging BFRs and natural compounds varied considerably according to the sampling site and reflected both the local anthropogenic impact of the region and the diversity/mass of biosynthesizers. The PBDE concentrations are lower than what was found for delphinids in the Northern Hemisphere around the same sampling period and most sampling sites presented mean concentrations lower than the limits for endocrine disruption known to date for marine mammals of 460 ng.g-1 lw, except for sampled from Santa Catarina state, in Southern Brazil. Conversely, MeO-BDE concentrations are higher than those of the Northern Hemisphere, particularly close to the Abrolhos Bans and Royal Charlotte formation, that are hotspots for biodiversity. Despite the elevated concentrations reported for this group, there is not much information regarding the effects of such elevated concentrations for these marine mammals. The distinct patterns observed along the Brazilian coast show that organobrominated compounds can be used to identify the ecological segregation of delphinids and that conservation actions should be planned considering the local threats.A.F. Azevedo and J. Lailson-Brito thank the National Council for Scientific and Technological Development (CNPq) for grants PQ-1B and 1D, respectively; and UERJ (Prociência). We thank the students from Aquatic Mammal and Bioindicator Lab (UERJ - Brazil), Environmental Chemistry Lab (CSIC - Spain) and Radioisotope Lab (UFRJ - Brazil). L.G. Vidal thanks the Coordination for the Improvement of Higher Education Personnel (CAPES - Finance Code 001) for providing her PhD grant. The authors thank the ICMBio - Estação Ecológica de Tamoios (ESEC Tamoios) and APA de Guapi-Mirim/ESEC da Guanabara for supporting the collection of carcasses in Ilha Grande Bay.Peer reviewe

Evidence confirms an anthropic origin of Amazonian Dark Earths.

Arising from: Silva et al. Nature Communications https://doi.org/10.1038/s41467-020-20184-2 (2021

In Vivo Effects Of The Controlled No Donor/scavenger Ruthenium Cyclam Complexes On Blood Pressure.

Ruthenium(II/III) complexes able to bind and release NO* were tested in vivo, in conscious Wistar rats instrumented for continuous blood pressure (BP) measurement and administration of in bolus injections (5 to 100 nmol/Kg i.v.) of trans-[Ru(II)Cl(NO+)(cyclam)](PF6)2 (cyclam-NO) or sodium nitroprusside (SNP). For normotensive rats, cyclam-NO produced a sustained 10% BP reduction of basal MAP during 7 +/- 0.4 to 11 +/- 0.3 min. In acute hypertensive rats, cyclam-NO produced BP reduction 3-fold larger than in normotensive rats and similar to that of SNP (maximal effect: 41 +/- 1.3 vs. 45 +/- 2.2 mmHg, respectively). However, the duration of the effect of cyclam-NO was 13 to 21-fold longer than that of SNP. The hypotensive effect of cyclam-NO was fully blocked in presence of continuous infusion of a NO* scavenger, carboxy-PTIO (6 mmol/Kg/min), or of the inhibitor of cGMP activation, methylene blue (83 nmol/Kg/min), or of the cyclam-NO precursor, trans-[RuCl(tfins)(cyclam)](tfms) (cyclam-tfms) (500 mmol/Kg/min). The long lasting BP reduction of cyclam-NO can be interpreted in terms of a slower rate of NO* release (k-NO = 2.2 x 10(-3) S(-1) at 35 degrees C) following chemical reduction (E(0') = 0.10 V vs NHE). In summary, cyclam-NO showed an hypotensive effect around 20 times longer than SNP in either normotensive or hypertensive rats, which was completely inhibited by methylene blue or carboxy-PTIO. Continuous infusion of cyclam-tfms completely blocked the hypotensive effect of cyclam-NO by scavenging the NO* released by the reduced cyclam-NO.702735-5

Climate Simulation and Change in the Brazilian Climate Model

Abstract The response of the global climate system to atmospheric CO2 concentration increase in time is scrutinized employing the Brazilian Earth System Model Ocean–Atmosphere version 2.3 (BESM-OA2.3). Through the achievement of over 2000 yr of coupled model integrations in ensemble mode, it is shown that the model simulates the signal of recent changes of global climate trends, depicting a steady atmospheric and oceanic temperature increase and corresponding marine ice retreat. The model simulations encompass the time period from 1960 to 2105, following the phase 5 of the Coupled Model Intercomparison Project (CMIP5) protocol. Notwithstanding the accurate reproduction of large-scale ocean–atmosphere coupled phenomena, like the ENSO phenomena over the equatorial Pacific and the interhemispheric gradient mode over the tropical Atlantic, the BESM-OA2.3 coupled model shows systematic errors on sea surface temperature and precipitation that resemble those of other global coupled climate models. Yet, the simulations demonstrate the model’s potential to contribute to the international efforts on global climate change research, sparking interest in global climate change research within the Brazilian climate modeling community, constituting a building block of the Brazilian Framework for Global Climate Change Research

Cellular Determinants of HIV Persistence on Antiretroviral Therapy

International audienceThe era of antiretroviral therapy has made HIV-1 infection a manageable chronic disease for those with access to treatment. Despite treatment, virus persists in tissue reservoirs seeded with long-lived infected cells that are resistant to cell death and immune recognition. Which cells contribute to this reservoir and which factors determine their persistence are central questions that need to be answered to achieve viral eradication. In this chapter, we describe how cell susceptibility to infection, resistance to cell death, and immune-mediated killing as well as natural cell life span and turnover potential are central components that allow persistence of different lymphoid and myeloid cell subsets that were recently identified as key players in harboring latent and actively replicating virus. The relative contribution of these subsets to persistence of viral reservoir is described, and the open questions are highlighted