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1.
Aeolian Res ; 55: 100786, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-35251380

RESUMO

While anthropogenic pollutants have decreased during the lockdown imposed as an effort to contain the spread of the Coronavirus disease 2019 (COVID-19), changes in particulate matter (PM) do not necessarily exhibit the same tendency. This is the case for the eastern Arabian Peninsula, where in March-June 2020, and with respect to the same period in 2016-2019, a 30 % increase in PM concentration is observed. A stronger than normal nocturnal low-level jet and subtropical jet over parts of Saudi Arabia, in response to anomalous convection over the tropical Indian Ocean, promoted enhanced and more frequent episodes of Shamal winds over the Arabian Peninsula. Increased surface winds associated with the downward mixing of momentum to the surface fostered, in turn, dust lifting and increased PM concentrations. The stronger low-level winds also favoured long-range transport of aerosols, changing the PM values downstream. The competing effects of reduced anthropogenic and increased dust concentrations leave a small positive signal (<5 W m-2) in the net surface radiation flux (Rnet), with the former dominating during daytime and the latter at night. However, in parts of the Arabian Gulf, Sea of Oman and Iran Rnet increased by >20 W m-2 with respect to the baseline period, owing to a clearer environment and weaker winds. It is concluded that a reduction in anthropogenic emissions due to the lockdown does not necessarily go hand in hand with lower particulate matter concentrations. Therefore, emissions reduction strategies need to account for feedback effects in order to reach the planned long-term outcomes.

2.
Air Qual Atmos Health ; 14(7): 1071-1079, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33841587

RESUMO

The preventive and cautionary measures taken by the UAE and Abu Dhabi governments to reduce the spread of the coronavirus disease (COVID-19) and promote social distancing have led to a reduction of mobility and a modification of economic and social activities. This paper provides statistical analysis of the air quality data monitored by the Environment Agency - Abu Dhabi (EAD) during the first 10 months of 2020, comparing the different stages of the preventive measures. Ground monitoring data is compared with satellite images and mobility indicators. The study shows a drastic decrease during lockdown in the concentration of the gaseous pollutants analysed (NO2, SO2, CO, and C6H6) that aligns with the results reported in other international cities and metropolitan areas. However, particulate matter (PM10 and PM2.5) averaged concentrations followed a markedly different trend from the gaseous pollutants, indicating a larger influence from natural events (sand and dust storms) and other anthropogenic sources. The ozone (O3) levels increased during the lockdown, showing the complexity of O3 formation. The end of lockdown led to an increase of the mobility and the air pollution; however, air pollutant concentrations remained in lower levels than during the same period of 2019. The results in this study show the large impact of human activities on the quality of air and present an opportunity for policymakers and decision-makers to design stimulus packages to overcome the economic slow-down, with strategies to accelerate the transition to resilient, low-emission economies and societies more connected to the nature that protect human health and the environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11869-021-01000-2.

3.
J Virol ; 83(17): 8722-32, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19553327

RESUMO

The presence of interleukin-2 (IL-2)-producing human immunodeficiency virus type 1 (HIV-1)-specific CD4(+) T-cell responses has been associated with the immunological control of HIV-1 replication; however, the causal relationship between these factors remains unclear. Here we show that IL-2-producing HIV-1-specific CD4(+) T cells can be cloned from acutely HIV-1-infected individuals. Despite the early presence of these cells, each of the individuals in the present study exhibited progressive disease, with one individual showing rapid progression. In this rapid progressor, three IL-2-producing HIV-1 Gag-specific CD4(+) T-cell responses were identified and mapped to the following optimal epitopes: HIVWASRELER, REPRGSDIAGT, and FRDYVDRFYKT. Responses to these epitopes in peripheral blood mononuclear cells were monitored longitudinally to >1 year postinfection, and contemporaneous circulating plasma viruses were sequenced. A variant of the FRDYVDRFYKT epitope sequence, FRDYVDQFYKT, was observed in 1/21 plasma viruses sequenced at 5 months postinfection and 1/10 viruses at 7 months postinfection. This variant failed to stimulate the corresponding CD4(+) T-cell clone and thus constitutes an escape mutant. Responses to each of the three Gag epitopes were rapidly lost, and this loss was accompanied by a loss of antigen-specific cells in the periphery as measured by using an FRDYVDRFYKT-presenting major histocompatibility complex class II tetramer. Highly active antiretroviral therapy was associated with the reemergence of FRDYVDRFYKT-specific cells by tetramer. Thus, our data support that IL-2-producing HIV-1-specific CD4(+) T-cell responses can exert immune pressure during early HIV-1 infection but that the inability of these responses to enforce enduring control of viral replication is related to the deletion and/or dysfunction of HIV-1-specific CD4(+) T cells rather than to the fixation of escape mutations at high frequencies.


Assuntos
Linfócitos T CD4-Positivos/imunologia , Infecções por HIV/imunologia , Infecções por HIV/virologia , HIV-1/genética , HIV-1/imunologia , Interleucina-2/metabolismo , Mutação de Sentido Incorreto/imunologia , Adulto , Animais , Mapeamento de Epitopos , Epitopos de Linfócito T/genética , Epitopos de Linfócito T/imunologia , HIV-1/isolamento & purificação , Humanos , Tolerância Imunológica , Estudos Longitudinais , Masculino , Produtos do Gene gag do Vírus da Imunodeficiência Humana/genética , Produtos do Gene gag do Vírus da Imunodeficiência Humana/imunologia
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