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1.
Geochem Trans ; 15(1): 2, 2014 Mar 19.
Artigo em Inglês | MEDLINE | ID: mdl-24641695

RESUMO

BACKGROUND: Coastal sediments in the northern Gulf of Mexico have a high potential of being contaminated by petroleum hydrocarbons, such as polycyclic aromatic hydrocarbons (PAHs), due to extensive petroleum exploration and transportation activities. In this study we evaluated the spatial distribution and contamination sources of PAHs, as well as the bioavailable fraction in the bulk PAH pool, in surface marsh and shelf sediments (top 5 cm) of the northern Gulf of Mexico. RESULTS: PAH concentrations in this region ranged from 100 to 856 ng g-1, with the highest concentrations in Mississippi River mouth sediments followed by marsh sediments and then the lowest concentrations in shelf sediments. The PAH concentrations correlated positively with atomic C/N ratios of sedimentary organic matter (OM), suggesting that terrestrial OM preferentially sorbs PAHs relative to marine OM. PAHs with 2 rings were more abundant than those with 5-6 rings in continental shelf sediments, while the opposite was found in marsh sediments. This distribution pattern suggests different contamination sources between shelf and marsh sediments. Based on diagnostic ratios of PAH isomers and principal component analysis, shelf sediment PAHs were petrogenic and those from marsh sediments were pyrogenic. The proportions of bioavailable PAHs in total PAHs were low, ranging from 0.02% to 0.06%, with higher fractions found in marsh than shelf sediments. CONCLUSION: PAH distribution and composition differences between marsh and shelf sediments were influenced by grain size, contamination sources, and the types of organic matter associated with PAHs. Concentrations of PAHs in the study area were below effects low-range, suggesting a low risk to organisms and limited transfer of PAHs into food web. From the source analysis, PAHs in shelf sediments mainly originated from direct petroleum contamination, while those in marsh sediments were from combustion of fossil fuels.

2.
Environ Pollut ; 214: 101-113, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27064616

RESUMO

In 2010, an estimate 4.1 million barrels of oil were accidentally released into the Gulf of Mexico (GoM) during the Deepwater Horizon (DWH) Oil Spill. One and a half years after this incident, a set of subtidal and intertidal marsh sediment cores were collected from five stations in Barataria Bay, Louisiana, USA, and analyzed to determine the spatial and vertical distributions and source of hydrocarbon residues based on their chemical composition. An archived core, collected before the DWH oil spill from the same area, was also analyzed to assess the pre-spill hydrocarbon distribution in the area. Analyses of aliphatic hydrocarbons, polycyclic aromatic hydrocarbons (PAHs) and stable carbon isotope showed that the distribution of petroleum hydrocarbons in Barataria Bay was patchy and limited in areal extent. Significant TPH and ΣPAH concentrations (77,399 µg/g and 219,065 ng/g, respectively) were detected in the surface sediments of one core (i.e., core A) to a depth of 9 cm. Based on a sedimentation rate of 0.39 cm yr(-1), determined using (137)Cs, the presence of anthropogenic hydrocarbons in these sediment core deposited ca. 50 to 60 years ago. The historical background hydrocarbon concentrations increased significantly at the sediment surface and can be attributed to recent inputs. Although the oil present in the bay's sediments has undergone moderate weathering, biomarker analyses performed on core A samples likely indicated the presence of hydrocarbons from the DWH oil spill. The effects of oiling events on Barataria Bay and other marsh ecosystems in this region remain uncertain, as oil undergoes weathering changes over time.


Assuntos
Monitoramento Ambiental , Sedimentos Geológicos/análise , Poluição por Petróleo/análise , Petróleo/análise , Hidrocarbonetos Policíclicos Aromáticos/análise , Poluentes Químicos da Água/análise , Baías/análise , Carbono/análise , Ecossistema , Sedimentos Geológicos/química , Golfo do México , Louisiana , Tempo (Meteorologia) , Áreas Alagadas
3.
Mar Environ Res ; 79: 100-10, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22763177

RESUMO

This study examined the influence of particle size and organic matter on aggregation and compaction of 3 hydraulically dredged sediments from coastal Louisiana (clay, silt loam, sandy loam) saturated under a range of salinity regimes (1 and 5 PSU, 5 and 10 PSU, and 15 and 25 PSU) for 4 time periods (1, 8, 16, and 26 weeks). Particle sizes were determined using a laser diffraction particle size analyzer, which allowed us to develop high-resolution results indicating changes in aggregate size across a spectrum of experimental conditions. The sediments with greater organic matter content exhibited approximately 60% aggregation, as indicated by fewer aggregates in the clay size fraction, and subsequently more aggregates in the sand size fraction, when organic matter remained in the sediment. Additionally, the sandy sediment compacted more than the organic sediments in the first 16 weeks. These findings suggest that sediments with greater clay and organic matter content behave as larger particles and may undergo particle rearrangement and compaction over longer time scales than sandy sediments with low organic matter. For coastal wetland restoration, models should include the effect of organic matter on particle aggregation to understand sediment dynamics over geologic time.


Assuntos
Monitoramento Ambiental , Sedimentos Geológicos/química , Recuperação e Remediação Ambiental , Água Doce , Sedimentos Geológicos/análise , Sedimentos Geológicos/microbiologia , Louisiana , Tamanho da Partícula , Salinidade , Água do Mar
4.
Mar Environ Res ; 72(5): 248-57, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22000271

RESUMO

Here we present results of an initial assessment of the impacts of a water diversion event on the concentrations and chemical composition of dissolved organic matter (DOM) and bacterioplankton community composition in Barataria Bay, Louisiana U.S.A, an important estuary within the Mississippi River Delta complex. Concentrations and spectral properties of DOM, as reflected by UV/visible absorbance and fluorescence, were strikingly similar at 26 sites sampled along transects near two western and two eastern areas of Barataria Bay in July and September 2010. In September 2010, dissolved organic carbon (DOC) was significantly higher (568.1-1043 µM C, x=755.6+/-117.7 µM C, n=14) than in July 2010 (249.1-577.1 µM C, x=383.7+/-98.31 µM C, n=14); conversely, Abs254 was consistently higher at every site in July (0.105-0.314) than in September (0.080-0.221), averaging 0.24±0.06 in July and 0.15±0.04 in September. Fluorescence data via the fluorescence index (FI450/500) revealed that only 30% (8 of 26) of the July samples had an FI450/500 above 1.36, compared to 96% (25 of 26) for the September samples. This indicates a more terrestrial origin for the July DOM. Bacterioplankton from eastern sites differed in composition from bacterioplankon in western sites in July. These differences appeared to result from reduced salinities caused by the freshwater diversion. Bacterioplankton communities in September differed from those in July, but no spatial structure was observed. Thus, the trends in bacterioplankton and DOM were likely due to changes in water masses (e.g., input of Mississippi River water in July and a return to estuarine waters in September). Discharge of water from the Davis Pond Freshwater Diversion (DPFD) through Barataria Bay may have partially mitigated some adverse effects of the oil spill, inasmuch as DOM is concerned.


Assuntos
Bactérias/classificação , Baías/análise , Carbono/análise , Água Doce , Microbiologia da Água , Bactérias/genética , Bactérias/isolamento & purificação , Baías/microbiologia , DNA Bacteriano/análise , Monitoramento Ambiental , Fluorescência , Louisiana , Oxigênio/análise , Poluição por Petróleo/prevenção & controle , Filogenia , Reação em Cadeia da Polimerase , Análise de Componente Principal , Salinidade , Espectrofotometria Ultravioleta , Temperatura
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