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1.
ACS Earth Space Chem ; 5(8)2021 Aug 10.
Artigo em Inglês | MEDLINE | ID: mdl-34497969

RESUMO

Overexposure to ultraviolet (UV) radiation is a threat to human health. It can cause skin cancer and cataracts. Human-made ozone-depleting substances (ODSs) reduce the ozone concentration in the Earth's stratosphere, which acts as a protective shield from UV radiation. To protect and restore the ozone layer, the Montreal Protocol on Substances that Deplete the Ozone Layer was enacted in 1987 to phase out the production and consumption of certain ODSs and was later amended and adjusted to significantly strengthen its requirements. The United States Environmental Protection Agency (EPA) uses its Atmospheric and Health Effects Framework (AHEF) model to assess the adverse human health effects associated with stratospheric ozone depletion and the U.S. health benefits from the global implementation of the Montreal Protocol. Comparing the Montreal Protocol as amended and adjusted with a scenario of no controls on ODSs showed the prevention of an estimated 443 million cases of skin cancer and 63 million cataract cases for people born in the United States between 1890 and 2100. In addition, 2.3 million skin cancer deaths are avoided. Compared with the original 1987 Montreal Protocol, strengthening the Montreal Protocol, through its subsequent amendments and adjustments, resulted in an estimated 230 million fewer skin cancer cases, 1.3 million fewer skin cancer deaths, and 33 million fewer cataract cases.

3.
Science ; 359(6377): 760-764, 2018 02 16.
Artigo em Inglês | MEDLINE | ID: mdl-29449485

RESUMO

A gap in emission inventories of urban volatile organic compound (VOC) sources, which contribute to regional ozone and aerosol burdens, has increased as transportation emissions in the United States and Europe have declined rapidly. A detailed mass balance demonstrates that the use of volatile chemical products (VCPs)-including pesticides, coatings, printing inks, adhesives, cleaning agents, and personal care products-now constitutes half of fossil fuel VOC emissions in industrialized cities. The high fraction of VCP emissions is consistent with observed urban outdoor and indoor air measurements. We show that human exposure to carbonaceous aerosols of fossil origin is transitioning away from transportation-related sources and toward VCPs. Existing U.S. regulations on VCPs emphasize mitigating ozone and air toxics, but they currently exempt many chemicals that lead to secondary organic aerosols.


Assuntos
Poluentes Atmosféricos/efeitos adversos , Exposição Ambiental , Hidrocarbonetos/efeitos adversos , Compostos Orgânicos Voláteis/efeitos adversos , Poluentes Atmosféricos/análise , Ácido Dioctil Sulfossuccínico , Humanos , Hidrocarbonetos/análise , Estados Unidos , Compostos Orgânicos Voláteis/análise
4.
Sci Rep ; 7(1): 13033, 2017 10 12.
Artigo em Inglês | MEDLINE | ID: mdl-29026153

RESUMO

Climate change is accelerating the release of dissolved organic matter (DOM) to inland and coastal waters through increases in precipitation, thawing of permafrost, and changes in vegetation. Our modeling approach suggests that the selective absorption of ultraviolet radiation (UV) by DOM decreases the valuable ecosystem service wherein sunlight inactivates waterborne pathogens. Here we highlight the sensitivity of waterborne pathogens of humans and wildlife to solar UV, and use the DNA action spectrum to model how differences in water transparency and incident sunlight alter the ability of UV to inactivate waterborne pathogens. A case study demonstrates how heavy precipitation events can reduce the solar inactivation potential in Lake Michigan, which provides drinking water to over 10 million people. These data suggest that widespread increases in DOM and consequent browning of surface waters reduce the potential for solar UV inactivation of pathogens, and increase exposure to infectious diseases in humans and wildlife.


Assuntos
Mudança Climática , Chuva , Energia Solar , Raios Ultravioleta , Microbiologia da Água , Surtos de Doenças , Humanos , Lagos/microbiologia , Lagos/parasitologia , Modelos Teóricos , Compostos Orgânicos/análise , Rios/química , Estações do Ano , Propriedades de Superfície
5.
Cancer Epidemiol Biomarkers Prev ; 23(10): 2145-52, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25069694

RESUMO

BACKGROUND: We previously reported a significant association between higher UV radiation exposure before diagnosis and greater survival with melanoma in a population-based study in Connecticut. We sought to evaluate the hypothesis that sun exposure before diagnosis was associated with greater survival in a larger, international population-based study with more detailed exposure information. METHODS: We conducted a multicenter, international population-based study in four countries-Australia, Italy, Canada, and the United States-with 3,578 cases of melanoma with an average of 7.4 years of follow-up. Measures of sun exposure included sunburn, intermittent exposure, hours of holiday sun exposure, hours of water-related outdoor activities, ambient ultraviolet B (280-320 nm) dose, histologic solar elastosis, and season of diagnosis. RESULTS: Results were not strongly supportive of the earlier hypothesis. Having had any sunburn in 1 year within 10 years of diagnosis was inversely associated with survival; solar elastosis-a measure of lifetime cumulative exposure-was not. In addition, none of the intermittent exposure measures-water-related activities and sunny holidays-were associated with melanoma-specific survival. Estimated ambient UVB dose was not associated with survival. CONCLUSION: Although there was an apparent protective effect of sunburns within 10 years of diagnosis, there was only weak evidence in this large, international, population-based study of melanoma that sun exposure before diagnosis is associated with greater melanoma-specific survival. IMPACT: This study adds to the evidence that sun exposure before melanoma diagnosis has little effect on survival with melanoma.


Assuntos
Melanoma/mortalidade , Neoplasias Cutâneas/mortalidade , Queimadura Solar/epidemiologia , Luz Solar/efeitos adversos , Feminino , Humanos , Masculino , Modelos de Riscos Proporcionais , Queimadura Solar/complicações
6.
Faraday Discuss ; 165: 105-22, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24600999

RESUMO

Secondary Organic Aerosols (SOA) production and ageing is a multigenerational oxidation process involving the formation of successive organic compounds with higher oxidation degree and lower vapor pressure. Intermediate Volatility Organic Compounds (IVOC) emitted to the atmosphere are expected to be a substantial source of SOA. These emitted IVOC constitute a complex mixture including linear, branched and cyclic alkanes. The explicit gas-phase oxidation mechanisms are here generated for various linear and branched C10-C22 alkanes using the GECKO-A (Generator for Explicit Chemistry and Kinetics of Organics in the Atmosphere) and SOA formation is investigated for various homologous series. Simulation results show that both the size and the branching of the carbon skeleton are dominant factors driving the SOA yield. However, branching appears to be of secondary importance for the particle oxidation state and composition. The effect of alkane molecular structure on SOA yields appears to be consistent with recent laboratory observations. The simulated SOA composition shows, however, an unexpected major contribution from multifunctional organic nitrates. Most SOA contributors simulated for the oxidation of the various homologous series are far too reduced to be categorized as highly oxygenated organic aerosols (OOA). On a carbon basis, the OOA yields never exceeded 10% regardless of carbon chain length, molecular structure or ageing time. This version of the model appears clearly unable to explain a large production of OOA from alkane precursors.


Assuntos
Aerossóis/química , Alcanos/química , Modelos Químicos , Estrutura Molecular , Compostos Orgânicos/química
8.
Cancer Epidemiol ; 35(6): e105-10, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21612999

RESUMO

BACKGROUND: Sunlight exposure increases risk of melanoma. Sunlight also potentiates cutaneous synthesis of vitamin D, which can inhibit melanoma cell growth and promote apoptosis. Vitamin D effects are mediated through the vitamin D receptor (VDR). We hypothesized that genetic variation in VDR affects the relationship of sun exposure to risk of a further melanoma in people who have already had one. METHODS: We investigated the interaction between VDR polymorphisms and sun exposure in a population-based multinational study comparing 1138 patients with a multiple (second or subsequent) primary melanoma (cases) to 2151 patients with a first primary melanoma (controls); essentially a case-control study of melanoma in a population of melanoma survivors. Sun exposure was assessed using a questionnaire and interview, and was shown to be associated with multiple primary melanoma. VDR was genotyped at the FokI and BsmI loci and the main effects of variants at these loci and their interactions with sun exposure were analyzed. RESULTS: Only the BsmI variant was associated with multiple primary melanoma (OR=1.27, 95% CI 0.99-1.62 for the homozygous variant genotype). Joint effects analyses showed highest ORs in the high exposure, homozygous variant BsmI genotype category for each sun exposure variable. Stratified analyses showed somewhat higher ORs for the homozygous BsmI variant genotype in people with high sun exposure than with low sun exposure. P values for interaction, however, were high. CONCLUSION: These results suggest that risk of multiple primary melanoma is increased in people who have the BsmI variant of VDR.


Assuntos
Predisposição Genética para Doença , Melanoma/genética , Receptores de Calcitriol/genética , Neoplasias Cutâneas/genética , Luz Solar/efeitos adversos , Idoso , Estudos de Casos e Controles , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fatores de Risco
9.
Cancer Epidemiol Biomarkers Prev ; 19(11): 2932-41, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20802019

RESUMO

BACKGROUND: Solar elastosis adjacent to melanomas in histologic sections is regarded as an indicator of sun exposure, although the associations of UV exposure and phenotype with solar elastosis are yet to be fully explored. METHODS: The study included 2,589 incident primary melanoma patients with assessment of histologic solar elastosis in the population-based Genes, Environment, and Melanoma study. Ambient erythemal UV (UVE) at places of residence and sun exposure hours, including body site-specific exposure, were collected. We examined the association of cumulative site-specific and non-site-specific sun exposure hours and ambient UVE with solar elastosis in multivariable models adjusted for age, sex, center, pigmentary characteristics, nevi, and, where relevant, body site. RESULTS: Solar elastosis was associated most strongly with site-specific UVE [odds ratio (OR) for top exposure quartile, 5.20; 95% confidence interval (95% CI), 3.40-7.96; P for trend <0.001] and also with site-specific sun exposure (OR for top quartile, 5.12; 95% CI, 3.35-7.83; P for trend <0.001). Older age (OR at >70 years, 7.69; 95% CI, 5.14-11.52; P for trend < 0.001) and having more than 10 back nevi (OR, 0.77; 95% CI, 0.61-0.97; P = 0.03) were independently associated with solar elastosis. CONCLUSION: Solar elastosis had a strong association with higher site-specific UVE dose, older age, and fewer nevi. IMPACT: Solar elastosis could be a useful biomarker of lifetime site-specific UV. Future research is needed to explore whether age represents more than simple accumulation of sun exposure and to determine why people with more nevi may be less prone to solar elastosis.


Assuntos
Tecido Elástico/patologia , Tecido Elástico/efeitos da radiação , Luz Solar/efeitos adversos , Fatores Etários , Feminino , Humanos , Masculino , Melanoma/etiologia , Melanoma/patologia , Pessoa de Meia-Idade , Razão de Chances , Fenótipo , Neoplasias Cutâneas/etiologia , Neoplasias Cutâneas/patologia , Pigmentação da Pele
10.
New Phytol ; 187(2): 417-425, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20456057

RESUMO

SUMMARY: *Several studies have reported in situ methane (CH(4)) emissions from vegetation foliage, but there remains considerable debate about its significance as a global source. Here, we report a study that evaluates the role of ultraviolet (UV) radiation-driven CH(4) emissions from foliar pectin as a global CH(4) source. *We combine a relationship for spectrally weighted CH(4) production from pectin with a global UV irradiation climatology model, satellite-derived leaf area index (LAI) and air temperature data to estimate the potential global CH(4) emissions from vegetation foliage. *Our results suggest that global foliar CH(4) emissions from UV-irradiated pectin could account for 0.2-1.0 Tg yr(-1), of which 60% is from tropical latitudes, corresponding to < 0.2% of total CH(4) sources. *Our estimate is one to two orders of magnitude lower than previous estimates of global foliar CH(4) emissions. Recent studies have reported that pectin is not the only molecular source of UV-driven CH(4) emissions and that other environmental stresses may also generate CH(4). Consequently, further evaluation of such mechanisms of CH(4) generation is needed to confirm the contribution of foliage to the global CH(4) budget.


Assuntos
Internacionalidade , Metano/análise , Folhas de Planta/metabolismo , Folhas de Planta/efeitos da radiação , Plantas/metabolismo , Plantas/efeitos da radiação , Raios Ultravioleta , Aerobiose/efeitos da radiação , Biomassa , Clima
11.
Cancer Epidemiol Biomarkers Prev ; 16(5): 991-7, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17507627

RESUMO

Malignant melanomas often contain BRAF or NRAS mutations, but the relationship of these mutations to ambient UV exposure in combination with phenotypic characteristics is unknown. In a population-based case series from North Carolina, 214 first primary invasive melanoma patients in the year 2000 were interviewed regarding their risk factors. Ambient solar UV exposures were estimated using residential histories and a satellite-based model. Cases were grouped on the basis of BRAF and NRAS somatic mutations, determined using single-strand conformation polymorphism analysis and radiolabeled DNA sequencing, and the risk profiles of these groups were compared. Mutually exclusive BRAF-mutant and NRAS-mutant cases occurred at frequencies of 43.0% and 13.6% with mean ages at diagnosis of 47.3 and 62.1 years, respectively. Tumors from patients with >14 back nevi were more likely to harbor either a BRAF mutation [age-adjusted odds ratio (OR), 3.2; 95% confidence interval (95% CI), 1.4-7.0] or an NRAS mutation (age-adjusted OR, 1.7; 95% CI, 0.6-4.8) compared with patients with 0 to 4 back nevi. However, BRAF-mutant and NRAS-mutant tumors were distinctive in that BRAF-mutant tumors were characteristic of patients with high early-life ambient UV exposure (adjusted OR, 2.6; 95% CI, 1.2-5.3). When ambient UV irradiance was analyzed by decadal age, high exposure at ages 0 to 20 years was associated with BRAF-mutant cases, whereas high exposure at ages 50 and 60 years was characteristic of NRAS-mutant cases. Our results suggest that although nevus propensity is important for the occurrence of both BRAF and NRAS-mutant melanomas, ambient UV irradiance influences risk differently based on the age of exposure. The association of BRAF mutations with early-life UV exposure provides evidence in support of childhood sun protection for melanoma prevention.


Assuntos
Melanoma/epidemiologia , Nevo/patologia , Proteínas Proto-Oncogênicas B-raf/genética , Neoplasias Cutâneas/epidemiologia , Raios Ultravioleta/efeitos adversos , Intervalos de Confiança , Análise Mutacional de DNA , DNA de Neoplasias/análise , DNA de Neoplasias/química , DNA de Neoplasias/genética , Feminino , Genes ras/genética , Humanos , Masculino , Melanoma/genética , Pessoa de Meia-Idade , Mutação , North Carolina/epidemiologia , Razão de Chances , Fenótipo , Polimorfismo Conformacional de Fita Simples , Fatores de Risco , Análise de Sequência de DNA , Neoplasias Cutâneas/genética
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