Sources, Vertical Fluxes, and Accumulation of Aliphatic Hydrocarbons in Coastal Sediments of the Río de la Plata Estuary, Argentina
详细信息    查看全文
文摘
Settling particles and underlying sediments collected at 1,2.5 and 4 km off the metropolitan Buenos Aires coastwere analyzed to evaluate the sources and accumulationof resolved (RES), unresolved (UCM), and biomarkeraliphatic hydrocarbons. Sedimentary aliphatic concentrations(RES 0.11-14 es/entities/mgr.gif">g·g-1; UCM 0.1-800 es/entities/mgr.gif">g·g-1) includedvariability associated with north-south gradients and anexponential offshore reduction. Highest concentrations wereregistered close to Buenos Aires port and sewer, comparedto cleaner northern stations and southward sites affectedby a seaward residue transport. Sediment traps deployedin the sewer area revealed large hydrocarbon (38 and319 mg·m-2·day-1, RES and UCM) and total organic carbonfluxes (29 ± 26 g·m-2·day-1). The composition of RESand hopanes evaluated by principal component analysisindicated a consistent offshore gradient defined by the relativecontribution of lower vs higher molecular weightcomponents. Distant sites showed decreasing proportionsof petrogenic n-C17-26 alkanes, isoprenoids, and C20-27terpanes and relative enrichment of n-C27,29,31,33 terrestrialplant alkanes and C31-33 homohopanes. Sedimenthydrocarbon profiles showed an average 2-fold reductiondown to 20 cm depth with preferential removal of lowermolecular weight components and enrichment of n-C23-35alkanes and hopanes. Sediment inventories and trapdepositional fluxes indicate the accumulation of 5800-9700 tons of aliphatic hydrocarbons in the top 0-5 cmsediments with a strong interfacial alteration and selectivepreservation of refractory components: n-C13-22 (1.0%)< isoprenoids (3.2%) < n-C23-35 (6.1%) < hopanes (47%)~ UCM (50%), compared to intermediate stability of organiccarbon (12%) and quantitative preservation of polychlorinatedbiphenyls (PCBs) (91%).

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700