Sundqvist Kristina L, Tysklind Mats, Cato Ingemar, Bignert Anders, Wiberg Karin
Department of Chemistry, Umeå University, 901 87, Umeå, Sweden.
Environ Sci Pollut Res Int. 2009 Jun;16(4):396-409. doi: 10.1007/s11356-009-0110-z. Epub 2009 Mar 19.
BACKGROUND, AIM, AND SCOPE: The primary aim of this study was to explore the variations in PCDD/F levels and homologue profiles of Baltic surface sediments by comprehensively analyzing polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) in samples from a large number of sites, encompassing not only previously known hotspot areas, but also sites near other potential PCDD/F sources, in pristine reference areas (in which there was no industrial activity) and offshore sites.
Surface sediment samples (146 in total) were collected at various points along the Swedish coast and offshore areas. In addition, bulk deposition was sampled, monthly, at a single site in northern Sweden during 1 year. The concentrations of tetra- through octa-substituted CDD/Fs were determined in both matrices.
Highly elevated concentrations of PCDD/Fs were found at many sites in coastal areas and concentrations were also slightly elevated in some offshore areas. Homologue profiles varied substantially amongst samples from coastal sites, while those from offshore and other pristine sediments were relatively similar. The offshore sediments showed different profiles from those observed in the deposition samples. Sediment levels of PCDD/Fs were not generally significantly correlated to organic carbon levels, except in some pristine areas. Comparison of data obtained in this and previous studies suggest that both their levels and profiles are similar today to those observed 20 years ago in coastal and offshore areas. The only detected trend is that their levels appear to have decreased slightly in the offshore area of the Bothnian Sea.
The localization of hotspot areas along the coast, the lack of consensus between PCDD/F profiles of sediments and general background, and their weak correlations with organic carbon suggest that PCDD/Fs in the study area largely originate from local/regional emissions. However, due to complicating factors such as sediment dynamics and land upheaval, it is not possible to conclude whether these pollutants derive from recent emissions or from a combination of recent emissions and re-distribution of previous inputs.
The results show that: elevated levels of PCDD/Fs are present in both coastal and offshore areas of the Baltic Sea, the major hotspots are close to the shore, and there are large variations in profiles, indicating that local emissions are (or have been) the major causes of pollution.
In order to identify other hotspot areas and trace sources, comprehensive analysis of PCDD/Fs in surface sediments is needed in all areas of the Baltic Sea that have not been previously investigated. The high levels of PCDD/Fs observed in surface sediments also indicate a need to elucidate whether they are due mainly to current emissions or a combination of recent pollution and re-distribution of historically deposited pollutants. To do so, better understanding of sediment dynamics and present-day inputs, such as riverine inputs, industrial effluents, and leakage from contaminated soil is required. There are indications that contaminated sediments have a regional impact on fish contamination levels. However, as yet there is no statistically robust evidence linking contaminated sediments with elevated levels in Baltic biota. It should also be noted that the Baltic Sea is being massively invaded by the deep-burrowing polychaete Marenzielleria ssp., whose presence in sediments has been shown to increase water concentrations of hydrophobic pollutants. In awareness of this, it is clear that high levels in sediments cannot be ignored in risk assessments. In order to investigate the emission trends more thoroughly, analysis of PCDD/Fs in offshore sediment cores throughout the Baltic Sea is also recommended.
背景、目的与范围:本研究的主要目的是通过全面分析来自大量地点的样品中的多氯二苯并 - 对 - 二噁英和多氯二苯并呋喃(PCDD/Fs),来探索波罗的海表层沉积物中PCDD/Fs水平及同系物分布的变化。这些地点不仅包括先前已知的热点区域,还包括其他潜在PCDD/Fs源附近的地点、原始参考区域(无工业活动)以及近海区域。
在瑞典海岸及近海区域的不同地点共采集了146份表层沉积物样品。此外,在瑞典北部的一个地点对大气沉降物进行了为期1年的月度采样。测定了两种基质中四至八取代CDD/Fs的浓度。
在沿海许多地点发现PCDD/Fs浓度大幅升高,一些近海区域的浓度也略有升高。沿海站点样品的同系物分布差异很大,而近海和其他原始沉积物的同系物分布相对相似。近海沉积物的分布与沉降物样品中观察到的不同。除了一些原始区域外,PCDD/Fs的沉积物水平一般与有机碳水平无显著相关性。本次研究及以往研究所得数据的比较表明,如今沿海和近海区域的PCDD/Fs水平及分布与20年前观察到的相似。唯一检测到的趋势是,波的尼亚海近海区域的PCDD/Fs水平似乎略有下降。
沿海热点区域的定位、沉积物PCDD/Fs分布与总体背景之间缺乏一致性以及它们与有机碳的弱相关性表明,研究区域内的PCDD/Fs主要源自本地/区域排放。然而,由于沉积物动态和陆地变迁等复杂因素,无法确定这些污染物是来自近期排放还是近期排放与先前输入物再分布的组合。
结果表明:波罗的海沿海和近海区域均存在PCDD/Fs水平升高的情况,主要热点靠近海岸,且分布存在很大差异,表明本地排放是(或曾经是)主要污染原因。
为了识别其他热点区域并追踪来源,需要对波罗的海所有先前未调查的区域的表层沉积物中的PCDD/Fs进行全面分析。在表层沉积物中观察到的高PCDD/Fs水平也表明需要阐明它们主要是由于当前排放还是近期污染与历史沉积污染物再分布的组合。为此,需要更好地了解沉积物动态和当前输入,如河流输入、工业废水和受污染土壤的渗漏。有迹象表明受污染的沉积物对鱼类污染水平有区域影响。然而,目前尚无统计学上有力的证据将受污染的沉积物与波罗的海生物群中升高的水平联系起来。还应注意的是,波罗的海正受到深穴多毛类动物Marenzielleria ssp.的大量入侵,沉积物中该物种的存在已被证明会增加疏水性污染物的水体浓度。鉴于此,很明显在风险评估中不能忽视沉积物中的高浓度污染物。为了更全面地调查排放趋势,还建议对整个波罗的海近海沉积物岩芯中的PCDD/Fs进行分析。