Distribution and sources of organochlorine pesticides in water and sediments from Daliao River estuary of Liaodong Bay,Bohai Sea (China)

The levels of 19 kinds of organochlorine pesticides (OCPs) in the aqueous phase, suspended particulate matter (SPM), pore water and sediments from Daliao River estuary of Liaodong Bay (Bohai Sea) in northeast China were investigated to evaluate their potential pollution risks. The total OCPs concentrations in the aqueous phase, SPM, pore water and sediments were 3.7–30.1 ng l⁻¹, 4.6–52.6 ng l⁻¹, 157–830 ng l⁻¹ and 2.1–21.3 ng g⁻¹ dry weight, respectively. The concentrations of OCPs, in the Daliao River estuary, are in the mid-range, as compared to those reported in other estuaries worldwide. The distribution of HCHs and DDTs were different indicating different contamination sources. Lindane is the main type of HCH and continuing use in northeast China of ‘pure’ HCH (lindane) rather than technical HCH accounts for the source. The ratios of (DDE + DDD)/DDT in the samples indicate no recent inputs of these chemicals to the estuary.     

渤海湾西部表层沉积物悬移组分元素特征及物源意义

对渤海湾西部海底表层沉积物样品粒径小于0.063mm的悬移组分进行16种元素测试,分析了各元素特征及分布规律。元素平均丰度与黄土及渤海泥质沉积物基本一致,说明渤海湾西部表层沉积物悬移组分的物源主要与黄河源区黄土高原的黄土有关。研究区16种元素可分为两类,I类是Sc、Co、Fe、V、Al、Ca、Mg、Th、U、Cr;II类是Zr、Hf、Ba、Na、Sr、K。同类元素丰度的平面分布规律相似,呈现正相关性;异类元素丰度的平面分布规律相反且呈负相关性。研究区主要分为两个地球化学分区,两区基本以北纬39°05′线为界,I区位于南部和中部,以高Sc、Co、V、Th、U、Cr、Fe、Al、Mg、Ca等I类元素为特征;而II区位于北部,以高Zr、Hf、Ba、Sr、Na、K等II类元素为特征。渤海湾西部表层沉积物悬移组分的元素特征及分区,可能与研究区内不同季节沿岸环流方向改变,进而导致不同物源母质沉积物输运混合作用有关。     

长江口海域悬浮颗粒有机物的稳定氮同位素分布及其生物地球化学意义

对2006年2,5,8,11月份长江口海域表层水体中的悬浮颗粒物(SPM)进行稳定氮同位素分析,根据不同季节、不同区域内其1δ5N值的变化研究水体中氮的迁移、转化等生物地球化学过程,揭示其环境行为,从而对该海域的氮循环机制进行探索。研究发现:该海域悬浮颗粒有机物的稳定氮同位素组成(1δ5Np)分布范围较宽,在0.6‰~8.2‰之间,具有明显的时空分布特点,反映了不同程度的陆源输入和氮的生物地球化学过程的影响。口门内,表层水体中1δ5Np的变化主要受长江径流的陆源输入影响,生物地球化学作用影响较弱;最大浑浊带,水体中的悬浮颗粒有机氮受微生物的降解活动影响明显,各季节均存在不同程度的颗粒物分解作用;外海区,陆源输入减弱,悬浮颗粒物的δ15Np值主要受微藻的同化吸收作用以及一定程度的颗粒物分解作用影响。     

基于高光谱数据的珠江口表层水体悬浮泥沙遥感反演模式

利用2006年12月4日珠江口海域实测的高光谱遥感反射率数据及悬浮泥沙质量浓度数据,进行了该海域表层水体悬浮泥沙遥感反演模式的研究。研究结果表明,悬浮泥沙质量浓度与Rrs(λ1)/Rr s(λ2)-Rrs(λ1)/Rrs(λ3)的相关性较好,其中Rrs(λ)代表遥感反射率,λ代表波长,λ1=762.6 nm,λ2=559.09 nm,λ3=772.78 nm,建立了悬浮泥沙质量浓度定量遥感反演模式,该模式的均方根误差为4.67 mg/L,可以用于珠江口海域的悬浮泥沙质量浓度的遥感监测。     

The fate of terrestrial organic matter in two Scottish sea lochs

Sea lochs are zones of rapid organic matter (OM) turnover. Most of this OM is of allochthonous origin, being introduced into the lochs via freshwater input. In this study the behaviour of terrestrially derived OM was elucidated using a combination of parameters which indicate OM diagenesis in the near surface sediments from two Scottish sea lochs, Loch Creran and Loch Etive. Alkaline CuO oxidation was used to determine lignin phenols which serve as biomarkers for terrestrial OM in sediments. Stable carbon isotope, total carbon and nitrogen and total OM (including the labile and refractory fractions) compositions were also determined.     

Petroleum pollution in surface sediments of Daya Bay,South China,revealed by chemical fingerprinting of aliphatic and alicyclic hydrocarbons

Nine surface sediments collected from Daya Bay have been Soxhlet-extracted with 2:1 (v/v) dichloromethane-methanol. The non-aromatic hydrocarbon (NAH) fraction of solvent extractable organic matter (EOM) and some bulk geochemical parameters have been analyzed to determine petroleum pollution of the bay. The NAH content varies from 32 to 276 μg g⁻¹ (average 104 μg g⁻¹) dry sediment and accounts for 5.8–64.1% (average 41.6%) of the EOM. n-Alkanes with carbon number ranging from 15 to 35 are identified to be derived from both biogenic and petrogenic sources in varying proportions. The contribution of marine authigenic input to the sedimentary n-alkanes is lower than the allochthonous input based on the average n-C₃₁/n-C₁₉ alkane ratio. 25.6–46.5% of the n-alkanes, with a mean of 35.6%, are contributed by vascular plant wax. Results of unresolved complex mixture, isoprenoid hydrocarbons, hopanes and steranes also suggest possible petroleum contamination. There is strong evidence of a common petroleum contamination source in the bay.     

水流挟沙力分析与探讨

水流挟沙力是悬沙输运计算中非常重要的问题之一,其计算形式常采用基于重力理论的经验和半经验公式.本文针对目前广泛采用的2种挟沙力关系式,选用4组实验水槽数据和2组天然河道实测资料分别讨论其关联性.结果表明,不论指数m在其取值范围内取何值,2个表达式皆存在一定的函数关联性.且当指数m取1和2/3时,直接表现出很强的线性关联.在挟沙力计算中采用流速的平方关系式,物理意义清晰,形式简单.在实际应用时,适当选取系数,挟沙力采用形式简单的平方关系式是完全可行的.     

闽江口入海悬沙输运的数值模拟

闽江河口位于福建省东部,本文利用欧拉-拉格朗日差分方法模拟闽江口及附近海域在不同径流下的潮流场,并建立拉格朗日水质点跟踪方法近似模拟了悬沙在海域中的迁移过程．水质点运动轨迹计算结果表明,闽江口悬沙在外海主要向南方或东南方输运,其轨迹呈现螺旋线．在洪峰流量下,悬沙运移距离较远．     

Skeletal linear extension rates of the foliose scleractinian coral Merulina ampliata (Ellis & Solander, 1786) in a turbid environment

Skeletal linear extension rates of a foliaceous, IndoPacific, skiophilous, heterotrophic, scleractinian Merulina ampliata (Ellis & Solander 1786) were obtained along a sediment/nutrient load gradient at the southern islands of Singapore. Measurements were made during November 1999– November 2000 using the alizarin red‐S staining technique. Suspended particulate matter concentration (r²_adj = 0.76), turbidity (r²_adj = 0.59), the organic content of suspended sediments (r² = 0.50), and nitrite‐nitrate concentration (r²_adj = 0.50) were significant predictors of the skeletal linear extension rate of M. ampliata. Maximum linear extension growth rates of M. ampliata (mean ± SD: 1.43 ± 0.67–3.26 ± 0.59 cm·year^?1) were comparable to 15‐year‐old accounts at the same research sites, indicating adaptation to low‐light, high‐sediment waters.     

Methylmercury production in sediments of Chesapeake Bay and the mid-Atlantic continental margin

Methylmercury (MeHg) concentration and production rates were studied in bottom sediments along the mainstem of Chesapeake Bay and on the adjoining continental shelf and slope. Our objectives were to 1) observe spatial and temporal changes in total mercury (HgT) and MeHg concentrations in the mid-Atlantic coastal region, 2) investigate biogeochemical factors that affect MeHg production, and 3) examine the potential of these sediments as sources of MeHg to coastal and open waters. Estuarine, shelf and slope sediments contained on average 0.5 to 1.5% Hg as MeHg (% MeHg), which increased significantly with salinity across our study site, with weak seasonal trends. Methylation rate constants (k_meth), estimated using enriched stable mercury isotope spikes to intact cores, showed a similar, but weaker, salinity trend, but strong seasonality, and was highly correlated with % MeHg. Together, these patterns suggest that some fraction of MeHg is preserved thru seasons, as found by others [Orihel, D.M., Paterson, M.J., Blanchfield, P.J., Bodaly, R.A., Gilmour, C.C., Hintelmann, H., 2008. Temporal changes in the distribution, methylation, and bioaccumulation of newly deposited mercury in an aquatic ecosystem. Environmental Pollution 154, 77] Similar to other ecosystems, methylation was most favored in sediment depth horizons where sulfate was available, but sulfide concentrations were low (between 0.1 and 10 μM). MeHg production was maximal at the sediment surface in the organic sediments of the upper and mid Bay where oxygen penetration was small, but was found at increasingly deeper depths, and across a wider vertical range, as salinity increased, where oxygen penetration was deeper. Vertical trends in MeHg production mirrored the deeper, vertically expanded redox boundary layers in these offshore sediments. The organic content of the sediments had a strong impact on the sediment:water partitioning of Hg, and therefore, on methylation rates. However, the HgT distribution coefficient (K_D) normalized to organic matter varied by more than an order of magnitude across the study area, suggesting an important role of organic matter quality in Hg sequestration. We hypothesize that the lower sulfur content organic matter of shelf and slope sediments has a lower binding capacity for Hg resulting in higher MeHg production, relative to sediments in the estuary. Substantially higher MeHg concentrations in pore water relative to the water column indicate all sites are sources of MeHg to the water column throughout the seasons studied. Calculated diffusional fluxes for MeHg averaged  1 pmol m^− 2 day^− 1. It is likely that the total MeHg flux in sediments of the lower Bay and continental margin are significantly higher than their estimated diffusive fluxes due to enhanced MeHg mobilization by biological and/or physical processes. Our flux estimates across the full salinity gradient of Chesapeake Bay and its adjacent slope and shelf strongly suggest that the flux from coastal sediments is of the same order as other sources and contributes substantially to the coastal MeHg budget.