Historical records and the sources of polycyclic aromatic hydrocarbons in the East China Sea

The coastal cities are the most advanced regions in China. In the past few decades, the environment changed very significantly due to large scale human activities in the coastal regions. Polycyclic aromatic hydrocarbons (PAHs) in three dated sediment cores from the west coast of the Yellow Sea (core A01), the Yangtze River estuary (YRE; core A02) and the Oujiang River estuary (ORE; core A03) were analyzed to reconstruct the environmental evolutionary process of the east China coastal region over the past century. In the three cores, PAHs concentrations were increased rapidly. Lower concentrations of PAHs were measured in core A02 than in cores A01 and A03. The vertical variation of PAHs in the YRE was dominated by the petrogenic sources. Historical records of PAHs in the ORE were controlled by pyrolytic sources. PAHs on the west coast of the Yellow Sea were contributed by the two sources.     

The distribution, sources and toxicity risks of polycyclic aromatic hydrocarbons and n-alkanes in riverine and estuarine core sediments from the Daliao River watershed

The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g^?1OC^?1 and 6.60 to 366.20 μg g^?1OC^?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQ_BaP) and dioxins (TEQ_TCDD) furnished a consistent assessment of the PAHs in the sediment cores.     

Polycyclic aromatic hydrocarbons in surface sediments of Laizhou Bay,Bohai Sea,China

Concentration, distribution, and sources of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of Laizhou Bay, China. Total PAH concentrations ranged from 97.2 to 204.8 ng/g, with a mean of 148.4 ng/g. High concentrations of PAHs were found in the fine-grained sediments on both sides of the Yellow River estuary (YRE). In contrast, low levels of PAHs were observed in relatively coarse grain sediments, suggesting hydrodynamics influence the accumulation of sedimentary PAHs. The YRE and its adjacent area is the main sink for Yellow River-derived PAHs. Both PAH isomer ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were applied to apportion sources of PAHs. Results indicated that both pyrogenic and petrogenic PAH sources were important. Further PCA/MLR analysis showed that the contributions of coal combustion, petroleum combustion and a combined source of spilled oil and biomass burning were 41, 15 and 44%, respectively. From an ecotoxicological viewpoint, the studied area appears to have low levels of PAH pollution.     

Sources and distribution of terrigenous organic matter delivered by the Atchafalaya River to sediments in the northern Gulf of Mexico

Suspended sediments (SS) from the Atchafalaya River (AR) and the Mississippi River and surficial sediment samples from seven shallow cross-shelf transects west of the AR in the northern Gulf of Mexico were examined using elemental (%OC, C/N), isotopic (δ¹³C, Δ¹⁴C), and terrigenous biomarker analyses. The organic matter (OM) delivered by the AR is isotopically enriched (∼−24.5‰) and relatively degraded, suggesting that soil-derived OM with a C4 signature is the predominant OM source for these SS. The shelf sediments display OC values that generally decrease seaward within each transect and westward, parallel to the coastline. A strong terrigenous C/N (29) signal is observed in sediments deposited close to the mouth of the river, but values along the remainder of the shelf fall within a narrow range (8-13), with no apparent offshore trends. Depleted stable carbon isotope (δ¹³C) values typical of C3 plant debris (−27‰) are found near the river mouth and become more enriched (−22 to −21‰) offshore. The spatial distribution of lignin in shelf sediments mirrors that of OC, with high lignin yields found inshore relative to that found offshore (water depth > 10 m).The isotopic and biomarker data indicate that at least two types of terrigenous OM are deposited within the study area. Relatively undegraded, C3 plant debris is deposited close to the mouth of the AR, whereas more degraded, isotopically enriched, soil-derived OM appears to be deposited along the remainder of the shelf. An important input from marine carbon is found at the stations offshore from the 10-m isobath. Quantification of the terrigenous component of sedimentary OM is complicated by the heterogeneous composition of the terrigenous end-member. A three-end-member mixing model is therefore required to more accurately evaluate the sources of OM deposited in the study area. The results of the mixing calculation indicate that terrigenous OM (soil-derived OM and vascular plant debris) accounts for ∼79% of the OM deposited as inshore sediments and 66% of OM deposited as offshore sediments. Importantly, the abundance of terrigenous OM is 40% higher in inshore sediments and nearly 85% higher in offshore sediments than indicated by a two-end-member mixing model. Such a result highlights the need to reevaluate the inputs and cycling of soil-derived OM in the coastal ocean.     

全新世渤海泥质沉积物地球化学特征

对渤海泥质区柱状沉积物的粒度与化学成分的分析及AMS 14C测年数据表明,全新世以来本区泥质沉积物的物质来源与沉积环境较为稳定.R型因子分析得出三种主要组合类型,以Ca、Ti和Mn为代表,分别对应黄河物质影响、陆源细粒物质输入和海洋自生作用.其中西南部与中部泥形成于约6000 a B.P.以来,黄河物质影响较强,主要在潮余流的作用下搬运后沉积下来.北部泥自早全新世之前便已开始形成,且主要沉积于高海面之前,受滦河物质作用相对较强.南部和北部泥质沉积年代存在明显差异,受水深、离岸距离、海平面高度等多种因素影响.尽管距黄河口较近,但区内沉积速率远低于中国近海其他泥质体,这与渤海环流状况及泥沙运移方向关系密切.     

Variability of tetraether lipids in Yellow River-dominated continental margin during the past eight decades: Implications for organic matter sources and river channel shifts

Glycerol dialkyl glycerol tetraethers (GDGTs) and bulk organic geochemical parameters were examined for a short core from the Bohai Sea, a Yellow River-dominated continental margin. A three end member mixing model using branched/isoprenoid tetraethers (BIT) index, δ¹³C and C/N shows that the average fractions of soil, marine and plant organic matter (OM) during the period of 1933–2011 are 67.7% (38–92%), 26.1% (0–58%) and 6.2% (0–23%), respectively. Abrupt changes of sedimentary OM compositions around 1953, 1976 and 1996 are synchronous with the Yellow River mouth relocations. The BIT index values (0.33–0.80) present a stronger correlation with crenarchaeol abundance (R² = 0.88) than branched GDGTs abundance (R² = 0.27), suggesting that variations of marine Thaumarchaeota abundance rather than soil OM inputs is the first order factor controlling the BIT index values, although this proxy has been widely used for soil OM. The comparison between the BIT index, nutrient status and historical Yellow River sediment load indicates that the high sensitivity of the BIT index to the Yellow River channel shifts cannot be explained by a nutrient stimulation mechanism, but instead is likely caused by the restriction of Thaumarchaeota growth in highly turbid water due to the enormous sediment inputs from Yellow River. Our study demonstrates that local conditions should be considered when applying the BIT index as an environmental proxy.     

现代黄河三角洲南部潮间带及附近海域沉积特征认识与分析

基于潮间带和浅海12个柱状样粒度、地球化学元素、210Pb同位素实测数据,结合河流年代特征、岸线历史变化等资料,参照前人关于沉积相和沉积速率研究成果,对现代黄河三角洲南部潮间带及莱州湾西部海域沉积特征进行了分析。根据剩余210Pb比活度信息,综合运用历史地理学方法、沉积环境判别公式和粒度曲线变化特征,初步认识了现代黄河三角洲南部潮间带地区具体沉积年代。对柱状样的数据进行分析后,运用相关特征值定量区分了沉积物的物源。结果表明:在潮间带这样不稳定的沉积环境下,210Pb_ex比活度阶段性倒置的分布模式虽然无法对年代进行连续标定,但可以在很大程度上指示沉积环境变化。现代黄河三角洲南部潮间带沉积物形成时间要远早于莱州湾西部,210Pb结合沉积环境判别函数、历史地理资料以及粒度特征可以将深度102 cm、80 cm、32 cm分别标定为1929年、1934年和1947年。广利河水系在深度20 cm范围内影响沉积环境。地球化学元素相关特征值分析显示:现代黄河三角洲南部潮间带沉积物风化程度介于黄河和莱州湾南岸之间,个别微量元素富集程度与莱州湾沉积物差异明显,就沉积环境而言,与现代黄河沉积物已有所不同。     

Chemical characteristics and pollution sources of petroleum hydrocarbons and PAHs in sediments from the Beiluohe River,Northern China

To determine the degree of hydrocarbon contamination and the contribution of local petroleum industries to contaminant loadings in sediments from the Beiluohe River, China, 12 surface sediment samples were collected for geochemical analysis in 2005. Sediment samples were extracted by organic solvents, separated by silica gel column chromatography and the profiles of n-alkanes, biomarkers and polycyclic aromatic hydrocarbons (PAHs) in sediments were analyzed by gas chromatography with flame ionization detector and gas chromatography/mass spectroscopy. Concentrations of total hydrocarbons in the sediments varied from 12.1 to 3,761.5 μg g⁻¹ dry wt, indicating that most sediments in Beiluohe River was only slightly to moderately contaminated by hydrocarbons. Concentrations of PAHs for six samples (sum of 16 isomers) varied from 17.7 to 407.7 ng g⁻¹ dry wt and at present low levels of PAHs did not cause adverse biological effects in Beiluohe River sedimentary environment. PAH compositions, n-alkanes and biomarker profiles all suggested that there were different sources of contaminations in studied areas. n-Alkanes reflect two distinct sources: a fossil n-alkane series from crude oil at sites S40, S43, S87 and plantwax n-alkanes at sites S39 and S45. Judged by their PAH ratios, the sediments at site S15 were pyrolytic, sediments at S17 and S43 were petrogenic, and sediments at S39, S40 and S64 had a mixture source of pyrolytic and petrogenic.     

Characterization and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in sediments in the Yellow River Estuary, China

Concentrations and sources of polycyclic aromatic hydrocarbons (PAHs) were investigated in surface sediments of the Yellow River Estuary (YRE). The isobath-parallel tidal and residual currents play important roles in the variation of PAH distribution, such that the contamination level of PAHs in fine-grained sediments is significantly higher than in the relatively coarse grain size sediments. Both diagnostic ratios and principal component analysis (PCA) with multivariate linear regression (MLR) were used to apportion sources of PAHs. The results revealed that pyrogenic sources are important sources of PAHs. Further analysis indicated that the contributions of coal combustion, traffic-related pollution and mixed sources (spills of oil products and vegetation combustion) were 35, 29 and 36 %, respectively, using PCA/MLR. Pyrogenic sources (coal combustion and traffic-related pollution) contribute 64 % of anthropogenic PAHs in sediments, which indicates that energy consumption could be a predominant factor in PAH pollution of YRE. Acenaphthylene and acenaphthene are the two main species of PAHs with more ecotoxicological concern in YRE.     

Nature of sedimentary organic matter in the lower reaches of the Godavari River basin, India

The distribution and nature of sedimentary organic matter (OM) have been examined in sediment cores collected from the lower reaches, including estuary, of the Godavari River in order to understand sedimentation patterns, sources, and diagenesis of OM. The samples were analyzed for organic carbon (Corg), total nitrogen, amino acids and hexosamines. The observed irregular trends in Corg distribution with depth indicate the unstable nature of bed sediment in the lower reaches of the river. Yet, in the lower estuarine region, regular trends in Corg distribution with depth reflect the deposition of sediment. The atomic ratio of Corg and total nitrogen (C/N; 10.5–16.1) also supported this observation. The distribution of amino acids and diagenetic indicators (β-ala+γ-aba mol.%, AA/HA and Glc-NH₂/Gal-NH₂) in individual cores revealed the post-depositional changes in the OM. In the core sediment from the lower reaches, there was no clear cut trend in amino acid content with depth. In the estuarine region, however, amino acid content was very low (50.5 and 186.5 μg g⁻¹) in the upper layers compared to that in the lower layers (558.5 and 1099.3 μg g⁻¹). Reactivity index (range 0.3–3.7) revealed that OM in the upper few centimeters, especially in the lower estuarine region, was more reactive relative to that in the deeper layers.     

渤海东部晚更新世以来的沉积物地球化学特征

为探讨渤海东部晚更新世以来的元素地球化学特征及控制因素,对渤海东部DLC70-1孔157个沉积物样品进行了化学成分、粒度及测年分析。结果表明,晚更新世以来研究区沉积物的物质来源与沉积环境较为稳定;根据DLC70-1孔沉积物地球化学特征,钻孔岩芯可划分为6层,反映了末次间冰期（暖期）晚期以来渤海东部沉积物物源的变化以及海面波动。Al₂O₃、MgO、TFe₂O₃、MnO、TiO₂、Cu、Zn、Pb、Cr和Rb等元素与细粒沉积物呈正相关,SiO₂、Na₂O与粗粒沉积物呈正相关,K₂O、Sr和Ba分布与沉积物粒度无明显正或负的相关性;R-型因子分析得出三种主要组合类型,以Mg、Sr和Ba为代表,分别对应陆源细粒物质输入与黄河物质、海河物质和滦河物质的影响。运用Ba/Al₂O₃与Sr/Al₂O₃、MgO/Al₂O₃与K₂O/Al₂O₃离散图分析了DLC70-1孔的物质来源,结果表明沉积物主要来源于黄河,该孔中上部32.30~49.00 m和9.30~23.20 m沉积物受到了滦河和海河物质的影响。     

Clay minerals in the major Chinese coastal estuaries and their provenance implications

A sea-survey was carried out along the Chinese coast from the Bohai Sea to South China Sea, and 15 surficial samples were taken from major coastal estuaries, i.e., from north to south, the Yellow, abandoned Yellow, Yangtze, Qiantang, Ou, Min, Han, and Pearl River estuaries. On the basis of clay mineral analysis and published data collection, this paper discusses the characteristics of clay minerals of each coastal river and potentials of implications of sediment sources. The results show that the change of diagnostic clay minerals from smectite to kaolinite from the Yellow to the Pearl River estuaries is southward, as clearly shown by the ratios of smectite to chlorite (S/Ch) and kaolinite to illite (K/I). S/Ch decreases southward, while K/I moves reversely, implying change in climate setting from cool/dry to humid/hot with intensified weathering processes. Besides, these two indicators in the estuaries are also linked with the derivation of parent-rock of each river-basin and coastal hydrodynamics. The disproportional higher ratio of K/I in the Yellow and abandoned Yellow River estuaries is ascribed to their sediment sources with abundant loess component in the north-central China. The K/I decrease offshore from the Pearl River estuary is primarily due to hydrodynamic sorting. Therefore, the S/Ch and K/I of the present study comprehensively reflect the controls of climate, parent-rock, and sediment transport along the coast.     

Black carbon in soils from different land use areas of Shanghai,China: Level,sources and relationship with polycyclic aromatic hydrocarbons

Black carbon (BC) in soils plays a key role of carrying hydrophobic pollutants like polycyclic aromatic hydrocarbons (PAHs). However, little is known about the spatial distribution, sources of BC and its relationship with PAHs in urban soils. We studied BC, total organic carbon (TOC) and PAHs concurrently in 77 soils collected from downtown area, suburban and rural area and industrial area of Shanghai, China. BC was determined by both chemical oxidation (dichromate oxidation, BC_Cr) and chemo-thermal oxidation (CTO-375, BC_CTO). BC sources were identified qualitatively by BC/TOC concentration ratios and BC-cogenerated high molecular weight (HMW) PAH isomer ratios and quantitatively by principal component analysis followed by multiple linear regression (PCA-MLR). Results showed that BC_Cr concentration (4.65 g/kg on average) was significantly higher than BC_CTO (1.91 g/kg on average) in Shanghai soils. BC_Cr concentrations in industrial area were significantly higher than those in other two. Stronger correlation was found between PAHs and TOC, BC_Cr than that between PAHs and BC_CTO, which indicates the possibility of PAHs being carried by charcoal and other organic matters thus negating its exclusive dependence on soot. Charcoal was therefore suggested to be taken into account in studies of BC and its sorption of PAHs. BC/TOC ratios showed a mixed source of biomass burning and fossil fuel combustion. PCA scores of BC-cogenerated HMW PAHs isomer ratios in potential sources and soil samples clearly demonstrated that sources of BC in urban soils may fall into two categories: coal and biomass combustion, and traffic (oil combustion and tire wear). PCA-MLR of HMW PAHs concentrations in soil samples indicated that coal and oil combustion had the largest contribution to BC in urban soils while tire wear and biomass combustion were important in downtown and rural area, respectively, which indicated they were main sources of HMW PAHs and presumably of BC.     

Concentrations and possible sources of PAHs in sediments from Bohai Bay and adjacent shelf

Concentrations, spatial distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency as priority pollutants were investigated in surface sediments of Bohai Bay, North China. Total concentrations of PAHs were in the range of 140.6–300.7 ng/g (dry wt), with an average of 188.0 ng/g. The three predominant PAHs were phenanthrene, acenaphthene and naphthalene. Sedimentary PAH concentrations of the north and central Bohai Bay were higher than those of the southern side of this bay. PAHs source analysis suggested that PAHs in most of the sediments were mainly from grass, wood and coal incomplete combustion. At other stations near the estuaries (Luanhe River Estuary and Chaohe River Estuary) or the oil drilling platform, both petrogenic and pyrogenic inputs were significant. The pyrogenic PAHs close to the oil drilling platform were mainly from petroleum combustion.     

Alkane and PAH biomarkers as tracers of terrigenous organic carbon in Arctic Ocean sediments

We present the first sedimentary biomarker study encompassing the entire Arctic Ocean. A large data set of organic markers for terrigenous, petroleum and combustion inputs [alkanes, hopanes and steranes, parent and alkyl polycyclic aromatic hydrocarbons (PAHs)] is examined for patterns in space and time using principal components analysis (PCA) and partial least squares (PLS). Biomarker patterns reveal the central Arctic Ocean basin sediments to be compositionally distinct from those of the Mackenzie River/Beaufort Sea and Barents Sea, but similar to those of the Laptev Sea. PAH distributions reflected in PAH ratios and PCA projections demonstrate that Arctic Ocean sediment is dominated by natural inputs to the extent that anthropogenic combustion PAHs are not significant. We find only modest changes between the glacial and post-glacial sediments for atmospherically transported hydrocarbon biomarkers, while particle associated biomarkers were captured strongly at basin edges during the glacial period, and much more evenly transported across basins during the post-glacial period. The orders of magnitude decreases in particle associated petrogenic alkanes and PAHs in central basins during glacial times, coupled with the uniformity of most petrogenic biomarker parameters for most basin and shelf locations, reflect a massive reduction in ice transport that makes the margins the most likely source of petrogenic material for the Pleistocene/Holocene central Arctic basins. The proximity of large coal deposits of various maturity levels along the Lena River, the overlap in PAH and biomarker composition of the Laptev Sea and surficial sediments from the central Arctic Ocean and the location of the Laptev Sea at the origin of the main Transpolar Drift all point to eroded coals from the Lena River/Laptev Sea as the likely source of petrogenic hydrocarbons to the central Arctic Ocean. The ubiquitous presence of allochthonous coal in Arctic Ocean surface sediments provides a major constraint on the use of petrogenic biomarkers to infer the presence of subsurface petroleum reserves.     

渤海湾晚更新世晚期以来古河道分布和三角洲发育及其古环境的演变

渤海湾及其沿岸是中国海洋地质与第四纪地质研究程度最高的地区之一。虽然研究成果众多,但仍有一些基础的地质问题亟待解决。比如,晚更新世晚期黄河是否流经渤海湾?全新世黄河在渤海湾及其沿岸形成的多期次三角洲叶瓣在海域如何展布?以上问题一直是中国海洋地质研究中备受关注的热点话题。借助2016-2017年在渤海湾获取的约2000 km的浅地层剖面数据、2个30 m左右的取芯钻孔（BXZK2017-1和BXZK2017-2孔）及相应的AMS ¹⁴C和OSL测年数据,同时结合前人的一些浅剖数据和钻孔的研究成果,将渤海湾中部晚更新世以来的地层自上而下划分出4个地震单元（SU1~SU4）和6个沉积单元（DU1-DU6）,分别对应前三角洲相、潮坪与浅海、泛滥平原、河道相、海陆交互相、湖沼相。在此基础上综合探讨渤海湾晚更新世晚期以来总体的地层框架和沉积演化特征。研究表明：黄河可能在21.8~9 cal ka BP,由近东西向流经渤海湾北部进入渤海中部盆地;全新世以来,渤海湾从西北侧至南侧,依次分布4期次的三角洲叶瓣,对应的发育时间可能分别是1400 AD~现在、11~1128 AD、700 BC~11 AD和1855~现在;渤海湾西侧最北两期次的水下三角洲可能主要与海河有关,而南侧其余2期次三角洲叶瓣则可能分别对应岐口超级叶瓣以及现代黄河三角洲超级叶瓣。加深了解渤海湾晚更新世晚期以来的地层序列演化、古河道发育以及全新世三角洲在渤海湾的展布情况,将有助于渤海湾海岸带开发、海底工程建设以及地质灾害防范等。     

近2600年来黄河下游沉积量和上中游产沙量变化过程

主要基于华北平原上93个钻孔中沉积物详细观测和分析数据,结合182组¹⁴C测年和埋深数据、参考前人黄河下游河道历史变迁及其他相关研究成果,估算出2600年以来黄河下游在602BC～11A.D.,11～1034A.D.,1034～1128A.D.,1128～1855A.D.和1855～1997A.D.等5个历史时期的年平均沉积量分别是3.89×10^8t/a,2.24×10^8t/a,6.63×10^8t/a,6.78×10^8t/a和8.47×10^8t/a。通过建立黄河下游有无堤防和决溢频率与泥沙输移比的关系,计算出5个时期黄河上中游的平均年输沙量分别是6.2×10^8t/a,6.8×10^8t/a,8.3×10^8t/a,11.5×10^8t/a和15.3×10^8t/a。进而探讨了黄河输沙量变化的主要原因,以及历史上王景治河后出现的600年安流时期的原因。     

Sediment distribution characteristics and environment evolution within 100 years in western Laizhou Bay,Bohai Sea,China

This study is about the reconstruction of fluvial origins based on the grain size distribution of sediment deposits in the western Laizhou Bay, Bohai Sea, China. Thirteen sediment cores were selected to research sediment characteristics using the Sahu discriminant formula, C-M diagram, and Folk method. The results showed: (1) Bounded by the Guangli River estuary, the north sediment was affected by the water and sand flowing from the Yellow River during different periods. The south sediment came from multi-source rivers under the influence of the Xiaoqing River, Mihe River, and other coastal rivers; (2) the deposited sediments were dated by a clear historical record of the branched channel oscillation combined with the characteristics of the diversion channel, erosion, and regression. The subaqueous delta overlapped during several Yellow River channel runs (1897–1904, 1929–1934, 1938–1947, 1947–1953, 1976–1996) and the deposited sediment facies changed (the north tidal flat-abandoned subaqueous delta-lateral delta-delta front); (3) the deposited sediment characteristics can be revealed by studying the branched diversions of the Yellow River and coastal multi-rivers of the past one hundred years.     

Contaminants in sediments from the central Gulf of Mexico

Surface sediment samples at 89 locations and 300-cm cores from 43 sites in the Mississippi Sound were examined for evidence of pollutant impact upon this coastal environment. Chemical variables determined were total organic carbon, Kjeldahl nitrogen, phenols, and hydrocarbons. Values of these pollutant indicators were about the same or lower in Gulf of Mexico samples compared to Missippi Sound sediments and considerably lower than those from rivers and bays emptying into the sound, indicating limited impact from sites of pollutant sources into the sound. Concentrations of sedimentary pollutants peaked in the Pascagoula River where levels of total organic carbon (TOC), Kjeldahl nitrogen (TKN), phenols, and hydrocarbons exceeded sound values by one to three orders of magnitude. Analysis of cores shows pollutant intrusion to sediment strata predating industrial development. The level of pollution varies from site to site but fortunately is only serious at localized sites within the sound.     

Sources and distribution of aliphatic and polycyclic aromatic hydrocarbons in Yellow River Delta Nature Reserve, China

Sediment samples collected from the Core Area, Experimental Area and Buffer Area of Yellow River Delta National Nature Reserve (YRDNNR), China, were analyzed by GC-MS in order to determine the degree of hydrocarbon contamination, and identify the sources of aliphatic hydrocarbons and PAHs. The total petroleum hydrocarbon contents of sediments were relatively low or moderate compared to world-wide locations reported to be chronically contaminated by oil. On the whole, the degree of petroleum contamination in the Core Area and Buffer Area in YRDNNR is weaker than that of the Experimental Area. The potential ecosystem risk assessment indicated that PAHs will not cause immediate adverse biological effects in the YRDNNR. Besides oil-related hydrocarbon inputs in this region, aliphatic hydrocarbon analysis showed the presence of hydrocarbons of terrestrial origin at some sampling sites, characterized by high CPI values. Based on PAH ratios and principal component analysis, pyrolytic input may be a major source of PAHs in YRDNNR sediment, while petrogenic inputs were more apparent at some sites in the Experimental Area due to oil exploration in the Shengli Oilfield.