Macdonald R W, Johannessen S C, Gobeil C, Wright C, Burd B, van Roodselaar A, Pedersen T F
Department of Fisheries and Oceans, Institute of Ocean Sciences, P.O. Box 6000, Sidney, BC, Canada V8L 4B2.
Mar Environ Res. 2008 Dec;66 Suppl:S87-100. doi: 10.1016/j.marenvres.2008.08.001. Epub 2008 Aug 12.
Organic carbon composition and redox element (Mn, Cd, U, Re, Mo, SigmaS, AVS) distributions are examined in seven 210Pb-dated box cores collected from the Strait of Georgia, British Columbia to evaluate the potential for redox elements to reveal impacts of anthropogenic loadings of labile organic carbon to sediments. In particular, the cores have been collected widely including regions far from local anthropogenic inputs and from locations within the zone of influence of two municipal outfalls where sediments are exposed to enhanced organic loadings from outfalls. We find a wide natural range in organic carbon forcing within the basin sediments generally reflected as Mn enrichments near the surface in cores exhibiting slow organic oxidation and sulphide, Cd, Mo, U and Re enrichments in cores exhibiting higher organic oxidation rates. Concentration profiles for redox elements or organic carbon are misleading by themselves, as they are influenced strongly by sediment porosity and sedimentation rate, and the organic matter remaining in sediment cores is predominantly recalcitrant. Fluxes of redox elements together with rates of organic metabolism estimated from sedimentation rates provide a better picture of the organic forcing. One core, GVRD-3, collected within the zone of influence of the Iona municipal outfall (0.5 km away), exhibits the highest organic carbon oxidation rates, enhanced Ag fluxes in the sediment surface mixed layer and altered delta15N composition, all of which implicate outfall particulates. Cd is also elevated in the GVRD-3 surface sediments, but evidence points to contamination and not redox forcing supporting this observation. Uranium also shows enrichment at sites near the outfalls, possibly in response to enhanced microbial metabolism. Predominantly these cores exhibit a wide natural range of organic carbon fluxes and organic carbon oxidation rates, supported by fluxes of marine and terrigenous organic carbon, within which it is difficult to identify any significant impact from municipal outfall organic carbon.
研究了从加拿大不列颠哥伦比亚省乔治亚海峡采集的7个210Pb测年箱式岩芯中的有机碳组成和氧化还原元素(锰、镉、铀、铼、钼、总硫、酸挥发性硫化物)分布,以评估氧化还原元素揭示不稳定有机碳人为负荷对沉积物影响的潜力。特别是,这些岩芯采集范围广泛,包括远离当地人为输入的区域以及两个市政排污口影响区内的地点,这些地点的沉积物受到排污口增加的有机负荷影响。我们发现,盆地沉积物中的有机碳强迫存在广泛的自然范围,通常表现为在有机氧化缓慢的岩芯中,表面附近锰富集;在有机氧化速率较高的岩芯中,硫化物、镉、钼、铀和铼富集。氧化还原元素或有机碳的浓度剖面本身具有误导性,因为它们受到沉积物孔隙率和沉积速率的强烈影响,并且沉积岩芯中残留的有机物质主要是难降解的。氧化还原元素通量以及根据沉积速率估算的有机代谢速率能更好地反映有机强迫情况。在伊奥纳市政排污口影响区内(距离0.5公里)采集的一个岩芯GVRD - 3,其有机碳氧化速率最高,沉积物表面混合层中的银通量增加,δ15N组成改变,所有这些都表明与排污口颗粒物有关。GVRD - 3表层沉积物中的镉也有所升高,但证据表明这是污染所致,而非氧化还原强迫支持这一观察结果。铀在排污口附近的地点也有富集,可能是对微生物代谢增强的响应。这些岩芯主要呈现出广泛的自然有机碳通量和有机碳氧化速率范围,由海洋和陆源有机碳通量支持,在此范围内很难识别出市政排污口有机碳的任何显著影响。