沉水植物对水-沉积物界面各形态氮含量的影响

在室内模拟条件下研究沉水植物对水-沉积物界面的上覆水、不同层次的间隙水和沉积物中不同形态氮含量的影响.结果表明:总体上,上覆水和间隙水中不同形态氮含量的顺序为有机氮＞氨氮＞硝态氮;沉积物中可交换态无机氮以氨氮为主,沉水植物的存在并没有改变这一格局.不同处理不同层次的间隙水中,各形态氮含量均为下层＞中层＞上层,但沉积物中氨氮和硝态氮含量变化规律不明显.水-沉积物界面氨氮和硝态氮含量呈现明显季节性变化.总之,水-沉积物界面氨氮是沉积物向上覆水扩散的主要氮组分,沉水植物降低了氨氮和硝态氮的扩散通量.     

Phosphate enrichment in the northern Gulf of Aqaba: Regulation by carbonate sediments and impact on nitrogen elevation

The effect of carbonate sediment in regulating phosphate concentrations in sea water was investigated by laboratory incubation experiments using different sediment types. Incubation experiments were made with two types of sediments: uncontaminated sediment from a marine reserve and contaminated sediment with deposited phosphate powders. Fluxes of inorganic nitrogen and phosphate were estimated from linear regressions of solute concentrations over incubation periods. Ammonium and phosphate fluxes were about twofold higher in the uncontaminated sediment that had significantly lower organic carbon and total phosphate concentrations than in the phosphate-contaminated sediment. To test the effect of dissolved phosphate on increasing nitrogen fixation, additional incubation experiments were carried out using treated carbonate and silicate sediments with added dissolved phosphate (20 μM). Incubations were made under sterile conditions with HgCl₂ added to distinguish between biologically enhanced processes and pure physicochemical processes. The adsorption rate of phosphate onto carbonate sediment was about twice that onto silicate sediments. No nitrogen elevation either as ammonium or as nitrate was observed in the soluble phosphate enrichment incubations. In conclusion, this study demonstrates the importance of the regulation of soluble phosphate concentrations in carbonate sediment environments where the carbonate sediment acts as a buffering system keeping soluble phosphate concentrations at certain steady-state levels. The study also demonstrates the lack of evidence on enhancement of nitrogen concentrations due to the increase phosphate concentrations.     

海洋沉积物-水界面营养盐交换过程的研究1

对胶州湾和渤海沉积物分别进行室内培养实验.结果表明,在沉积物中加入营养盐后,铵氮、硅酸盐由沉积物向水体的迁移增大,铵氮的迁移在总溶解态氮的交换中起主要作用,其交换量约占总溶解态氮扩散量的76%,硝酸盐及磷酸盐由水体向沉积物的迁移减弱.在上覆水中加入营养盐后,硝酸盐、磷酸盐由水体向沉积物的迁移增大,硝酸氮的迁移占总溶解态氮交换的主要部分,约为62%.铵由沉积物向水体的迁移减弱,硅酸盐变成由水体向沉积物迁移.沉积物对于上覆水中营养盐的浓度具有一定的调节作用.无论在充空气或充氮气条件下,磷及硅的交换速率变化不明显,铵氮的迁移占总溶解态氮扩散量的98%以上.充氧条件下硝酸盐由沉积物向上覆水的迁移通量较充氮气条件增加.比较两种不同的通量计算方法(积分和拟合),结果表明由两种计算方法计算的交换速率的变化趋势基本是一致的.     

FORMS OF NITROGEN (NO 3 - -N; NO 2 - -N AND NH 2 CONH 2 -N) AND THEIR RELATIONS TO A.O.U. IN THE INDIAN COASTAL WATERS OF ARABIAN SEA

The distribution of three important dissolved forms of nitrogen, viz. nitrate, nitrite and urea in the surface and bottom water samples collected from 27 selected hydrographic profiles, in the Arabian Sea, along the west coast of India is described. Of the three forms, nitrate concentrations were the highest and comparatively higher concentrations were observed in the bottom water. Decomposition of organic matter resulting in the release of the thermodynamically stable nitrogen species, i.e. nitrate, may be the major factor resulting in higher nitrate concentrations at these depths, where the water is also characterized by low values of dissolved oxygen and temperature. The significant positive correlation between A.O.U. and nitrate of the bottom water samples emphasizes the role of oxidative decomposition of organic matter which plays an active role in reducing the oxygen concentrations below the theoretical values since at this depth ( ≈200 m) the net production is taken to be zero. This is also evidenced by the negative correlation of nitrate with dissolved oxygen and temperature, for the bottom samples.     

水动力条件下苦草对沉积物氮释放的影响

在浅水湖泊中,沉积物易受到水流的扰动释放出原本沉降于其中的氮营养盐。沉水植物一方面能够减少水动力的作用,一方面又能够吸收沉积物中的和已经释放到上覆水中的氮营养盐供其生长同时改善水质。因此,研究沉水植物对沉积物中氮营养盐释放的影响具有很重要的实际意义。借助自主开发的生态水槽,研究苦草（Vallisneria spiraslis L.）在动、静水条件下对沉积物氮的释放的影响。实验装置包括四组水槽,两组动水槽中的一组只铺沉积物,另一组在沉积物上种植苦草,两组静水槽也如此设置。在40 d的实验周期内,我们在实验始末采集沉积物样品,在每一个采样时间点（0、1、3、6、12、20、30、40 d）采集水样,并测定沉积物中总氮含量,原水样中的总氮含量以及过滤水样中的总氮、氨氮、硝氮和亚硝氮的含量。研究结果表明：没有苦草的实验组0～1 cm沉积物层总氮下降幅度较大,有苦草的实验组表面0～1 cm沉积物层氮含量较高。苦草从根系周围沉积物中吸收氮,1～4 cm沉积物层的吸收量多于4～8 cm沉积物层。各水槽上覆水中总氮含量在第1天就有较大的增加,从0.09 mg·L^-1分别升到0.60、0.50、0.379、0.36 mg·L^-1在水动力影响下的增加更显著,后缓慢上升。动水槽中进入到上覆水的氮中80%以上是以溶解态氮形式存在,静水槽中这个比例高达90%以上。苦草对溶解态和颗粒态氮的去除率最高可达27.6%和84.3%。3种氮形态中硝态氮的含量比重较大,在动水条件下,苦草对氨氮,硝氮和亚硝氮的去除率最高可达30.0%、25.0%和60.0%。但苦草对水中氮形态的比例的影响并不明显。以上结果说明水动力条件明显促进沉积物中氮的释放,沉水植物苦草通过保护表层沉积物,吸收下层沉积物中氮,去除进入上覆水中的氮,特别是颗粒态氮和溶解态中的亚硝态     

Forms of Nitrogen (NO 3 - -N; NO 2 - -N and NH 2 CONH 2 -N) and their relations to A.O.U. in the Indian coastal waters of Arabian Sea

The distribution of three important dissolved forms of nitrogen, viz. nitrate, nitrite and urea in the surface and bottom water samples collected from 27 selected hydrographic profiles, in the Arabian Sea, along the west coast of India is described. Of the three forms, nitrate concentrations were the highest and comparatively higher concentrations were observed in the bottom water. Decomposition of organic matter resulting in the release of the thermodynamically stable nitrogen species, i.e. nitrate, may be the major factor resulting in higher nitrate concentrations at these depths, where the water is also characterized by low values of dissolved oxygen and temperature. The significant positive correlation between A.O.U. and nitrate of the bottom water samples emphasizes the role of oxidative decomposition of organic matter which plays an active role in reducing the oxygen concentrations below the theoretical values since at this depth ( , 200 m) the net production is taken to be zero. This is also evidenced by the negative correlation of nitrate with dissolved oxygen and temperature, for the bottom samples.     

Hydrocarbon bioaccumulation from contaminated sediment by the deposit-feeding polychaeteAbarenicola pacifica

This study examines the role of the organic carbon content of sediment in aromatic hydrocarbon bioaccumulation and assesses the importance of two routes of hydrocarbon uptake: (1) the uptake of the particulate contaminant fraction from ingested sediment; (2) the uptake of the dissolved contaminant fraction from interstitial or overlying water. The lugwormAbarenicola pacifica was collected from San Juan Island, Washington, USA, in January 1989, and exposed to three sediments contaminated with [³H]benzo (a) pyrene (BaP). By manipulating the organic content of these sediments, it was possible to establish three treatments with similar BaP concentrations in the interstitial water, but differing in the amount of BaP in the bulk sediment. BaP bioaccumulation over the first few days of exposure was correlated with feeding rate, suggesting that ingested sediments were a source of BaP. The greatest body burden, however, was attained in those individuals held in sediments with the lowest organic carbon content and the lowest BaP concentration. Body burden at steady state was not correlated with either BaP concentrations in bulk sediment (dry weight or organic carbon-normalized bases) or the interstitial water. Increased organic matter decreased BaP bioavailability in a non-linear fashion. Bioaccumulation factors relative to water and organic content were relatively constant between 1 and 2% organic carbon in the sediment, but these same accumulation factors substantially underestimated body burden if applied to sandy sediments with little (0.3%) organic carbon.     

不同溶氧条件下九龙江口湿地沉积物一水界面氨氮释放与氧化规律

摘要：沉积物中氨氮（NH4^＋-N）的释放与氧化是河口湿地生态系统氮素生物地球化学循环的关键过程。本文通过室内模拟,构建饱和（BH）、好氧（HY）、缺氧（QY）和厌氧（YY）等四种上覆水溶氧（DO）条件,研究九龙江口湿地两种沉积物（红树林、光滩）中NH4^＋-N在沉积物-水界面的释放与氧化规律。结果表明,不同溶氧条件下,两种沉积物氨氮的释放、氧化存在显著差异。首先,红树林沉积物上覆水NH4^＋-NN的累积释放量是光滩沉积物的1．9-4．5倍,其中红树林沉积物上覆水NH4LN释放量分别达到1．64mg（BH）、2．07mg（HY）、3．47mg（QY）和3．20mg（YY）,而光滩沉积物则分别为0．85mg（BH）、1．00mg（HY）、0．77mg（QY）和1．27mg（YY）。在较高DO条件下两种沉积物NH。’一N均呈低释放状态,而在较低DO条件下则呈高释放状态。另外,四种溶氧条件下红树林沉积物NH4^＋-NN的释放速率（N43．73-78．51mg-m^-2-d^-1）和氧化速率（N26．19-40．68mg-m^-2-d^-1）均高于光滩（分别为N14．50-19．22mg-m^-2-d^-1和N8．89-22．53mg-m^-2-d^-1）,原因可能是红树林沉积物微生物种类丰富,群落多样性更高,矿化和硝化作用强烈。本文明晰了不同溶氧条件下河口红树林湿地沉积物NH4^＋-N的迁移转化过程,可促进滨海湿地的生态保护以及近海水域富营养化的控制。     

Revealing the factors affecting occurrence and distribution of polycyclic aromatic hydrocarbons in water and sediments of Lake Baikal and its tributaries

The concentrations of polycyclic aromatic hydrocarbons (PAH), total carbon (TC), total organic carbon (TOC), total nitrogen (TN) and dissolved inorganic nitrogen (DIN) in water and sediments of Lake Baikal and its tributaries were measured. It was found that according to existing water and sediment quality standards limiting permissible PAH concentrations, both surface waters and sediments in Lake Baikal watershed can be considered as unpolluted with PAHs compounds. Nevertheless, the spatial distribution of PAH concentrations in lake water indicates the existence of some point PAH sources in and around the lake. These sources were natural oil seeps and communal facilities such as residential coal-fired and oil-fired boilers. It was observed that concentrations of PAHs in both water and sediments are controlled by organic matter content and organic matter mineralisation degree, as indicated by PAH-to-carbon and nitrogen-to-carbon ratios respectively. It was found that PAH/TOC and PAH/TC ratios characterise PAH loading on water and sediments respectively, whereas DIN/TOC and TN/TC ratios characterise self-purification of water and sediments respectively. It was proved that PAH/TOC and DIN/TOC ratios can be used as tracers to evaluate the PAH contributions from tributaries to Lake Baikal.     

Environmental risk assessment of cobalt and manganese from industrial sources in an estuarine system

A total of 74 samples of soil, sediment, industrial sludge, and surface water were collected in a Mediterranean estuarine system in order to assess the potential ecological impact of elevated concentrations of Co and Mn associated with a Terephthalic (PTA) and Isophthalic (PIPA) acids production plant. Samples were analyzed for elemental composition (37 elements), pH, redox potential, organic carbon, and CaCO₃ content, and a group of 16 selected samples were additionally subjected to a Tessier sequential extraction. Co and Mn soil concentrations were significantly higher inside the industrial facility and around its perimeter than in background samples, and maximum dissolved Co and Mn concentrations were found in a creek near the plant’s discharge point, reaching values 17,700 and 156 times higher than their respective background concentrations. The ecological risk was evaluated as a function of Co and Mn fractionation and bioavailability which were controlled by the environmental conditions generated by the advance of seawater into the estuarine system during high tide. Co appeared to precipitate near the river mouth due to the pH increase produced by the influence of seawater intrusion, reaching hazardous concentrations in sediments. In terms of their bioavailability and the corresponding risk assessment code, both Co and Mn present sediment concentrations that result in medium to high ecological risk whereas water concentrations of both elements reach values that more than double their corresponding Secondary Acute Values.     

曝气复氧对富营养化水体底泥氮磷释放的影响

采用实验室模拟，研究了曝气复氧对富营养化水体底泥氮磷释放的影响，结果表明，①溶解氧是影响底泥氮磷释放的重要因素，厌氧状态会加速底泥氮磷的释放。②正常条件下曝气复氧可以有效的控制底泥总磷的释放；曝气条件下高pH值无法控制底泥总磷的释放，搅动会对底泥总磷的释放产生轻微的影响，上覆水总磷浓度较高时底泥会发生吸磷现象，而温度则影响较小。③正常条件下曝气复氧可以控制比较封闭水体底泥氨氮的释放；曝气条件下温度对底泥氨氮和总氮的释放影响较大，即温度越高，抑制氨氮和总氮的释放效果越好，且低温会导致底泥氨氮和总氮的大量释放；曝气条件下搅动导致底泥释放更多的氨氮和总氮。     

广东省不同水库底泥理化性质对内源氮磷释放影响

采用分级浸取分离方法,分析了广东省10个典型水库底泥的氮磷营养形态分布和污染状况;并通过模拟覆水试验,研究了不同水库底泥氮磷形态及理化性质对内源氮磷释放的影响。结果表明：广东省10个水库底泥氮磷污染较为严重,全氮含量为0.33~3.31 g.kg^-1,平均值为1.70 g.kg^-1;全磷含量为0.14~2.63 g.kg^-1,平均值为1.31 g.kg^-1。底泥氮磷主要以可转化态形式存在,可转化态氮磷含量占总氮磷含量百分比分别为41.2%~71.4%和53.6%~93.2%。底泥内源氮磷的释放主要受氮磷的赋存形态和含量的影响,水库底泥总氮的释放量与离子交换态氮（IEF-N）、碳酸盐结合态氮（WAEF-N）、铁锰氧化物结合态氮（SAEF-N）呈极显著正相关关系,相关系数分别为0.931、0.814、0.807;总磷的释放量与碳酸盐结合态磷（WAEF-P）、铁锰氧化物结合态磷（SAEF-P）呈极显著正相关,相关系数分别为0.960、0.957;这几种氮磷形态是上覆水体中氮磷的重要来源。同时底泥内源氮磷释放还与底泥机械组成有关,其中总氮和总磷释放量与底泥黏粒质量分数呈显著正相关,相关系数分别为0.738、0.638;而总氮的释放量与底泥砂粒质量分数呈显著负相关,相关系数为-0.685。这可能与可转化态氮磷更多的分布在细粒级底泥中有关,细颗粒底泥氮磷释放是上覆水体氮磷的主要来源。     

南黄海不同粒度表层沉积物中可转化氮与环境因子的关系

南黄海不同粒度表层沉积物中可转化氮的形成与释放受环境因子的驱动作用各不相同,上覆水体的温度、盐度、pH值、DO的含量以及NH4^ 和NO3^-的含量都对其有一定的影响．其中DO是不同形态的氮形成与释放最显著的影响因素,这是因为上覆水体中DO的含量愈高,扩散进入表层沉积物中的O2就愈多,沉积物处于相对氧化的环境中,有机质的矿化作用较易进行,致使无机形态氮的含量相对较高,而有机形态氮的含量相对较低,所以其与可转化有机形态氮呈负相关,而与可转化无机形态氮呈正相关．温度与中、细粒度沉积物中的SOEF-N的含量呈显著正相关,可能是因为温度的升高加快了海洋底栖生物的生长发育,使生物排泄物和死亡残体增多,尽管温度的升高加快了沉积物中有机质的矿化分解,但由于中、细粒度沉积物堆积紧密,对温度的响应不明显,致使SOEF-N的含量随温度的升高而升高．上覆水体中的NH;和NO3^-分别与中、细粒度沉积物中的SAEF-N和SOEF-N的含量呈正相关,说明上覆水体中的NH4^ 和NO3^-主要来自于沉积物中SAEF-N和SOEF-N的形成与释放．另外,粗粒度沉积物中不同形态的氮对环境的响应较中、细粒度沉积物中的强．     

Spatial distribution of phosphorus forms in sediments with different distances to the estuary of the Dianchi Lake,China

Effects of human activity on the distribution of phosphorus (P) forms were investigated for the sediments and porewaters in Daqinghe Estuary of Dianchi Lake, China. The concentrations of total P (TP), inorganic-P (I-P),and organic-P (Org-P), and the ratio of iron-bound P (Fe-P)/calcium-bound P (Ca-P) in the sediments decreased with the increasing distance from the sampling site to the estuary. This is probably due to the flocculant materials, e.g., ferric and aluminous salts, usually being added in the wastewater treatment processes. The concentration of ammonia in the sediment porewaters significantly decreased with the increasing distance from the sampling site to the estuary. Both concentrations of total nitrogen and nitrogen in the sediment porewaters decreased to some content with the increasing distance from the sampling site to the estuary. However, the concentrations of nitrate, dissolved total P (DTP), and TP did not have strong relationship with the distances from the sampling sites to the estuary. Pollution load and water quantity also had an important influence on the concentrations of P in sediments and its interstitial water in estuary sedimentary area.     

Nitrogen dynamics in the sediments of a wetland coastal ecosystem of southern India

The study area, Kuttanad Waters is a part of the Cochin estuarine system on the west coast of India. Kuttanad is well known for its agricultural activity and so the major contribution to the inorganic ions of nitrogen will be from fertilisers applied in agriculture. Based on observed salinity the stations have been divided into three zones. The fresh water zones had higher quantities of silt and clay whereas the estuarine zone was more sandy. The chemical speciation scheme applied here distinguishes three forms of ammoniacal nitrogen species: exchangeable, fixed, and organic ammoniacal nitrogen. No significant trends were observed in the seasonal distribution of total, exchangeable, fixed and organic nitrogen. A significant concentration of exchangeable ammonia was observed in the sediment due to their predominantly reducing environment, which restricts nitrification. High NH₄-N concentrations in the pore waters, along with the sedimentary composition leads to a significantly high quantity of fixed NH₄-N. The low values for N org is due to high mineralisation or deamination of organic nitrogen     

Nitrogen dynamics in the sediments of a wetland coastal ecosystem of southern India

The study area, Kuttanad Waters is a part of the Cochin estuarine system on the west coast of India. Kuttanad is well known for its agricultural activity and so the major contribution to the inorganic ions of nitrogen will be from fertilisers applied in agriculture. Based on observed salinity the stations have been divided into three zones. The fresh water zones had higher quantities of silt and clay whereas the estuarine zone was more sandy. The chemical speciation scheme applied here distinguishes three forms of ammoniacal nitrogen species: exchangeable, fixed, and organic ammoniacal nitrogen. No significant trends were observed in the seasonal distribution of total, exchangeable, fixed and organic nitrogen. A significant concentration of exchangeable ammonia was observed in the sediment due to their predominantly reducing environment, which restricts nitrification. High NH₄-N concentrations in the pore waters, along with the sedimentary composition leads to a significantly high quantity of fixed NH₄-N. The low values for N org is due to high mineralisation or deamination of organic nitrogen     

鄱阳湖沉积物中磷吸附释放特性及影响因素研究

沉积物是氮磷营养盐的主要蓄积库,它不仅是外来污染物的归宿地,同时其自身营养盐的释放也可对水环境产生重大影响。针对鄱阳湖存在的沉积物磷释放问题,关键环境因子对基质磷吸附的影响规律进行了探讨。通过控制在不同环境因素条件下,上覆水中磷的变化规律探讨,阐明磷在上覆水-底泥界面迁移转化的规律和环境因素对迁移转化过程的影响。研究结果表明,吸附初始阶段,两者含量相差较大,起始吸附速率很高;随着反应时间的推进,两者含量差随之减小;当吸附时间达到30 min时,此时上覆水的平衡质量浓度为8.648 mg·L^-1,两者含量达成平衡。由磷的吸附等温试验同样可看出,随着平衡质量浓度逐渐增加,土壤吸磷量刚开始增加较快,随后增加趋势逐渐减缓直至磷饱和。pH越小,上覆水质量浓度越低,沉积物对磷的吸附作用越强;pH越大,上覆水中TP质量浓度越大,强碱条件下,TP吸收量剧减。在好氧条件下,沉积物对磷的吸附远远高于厌氧条件下沉积物的吸附。好氧条件下,反应在4 h内,沉积物对磷的吸附速率最高,随后吸附量很小直至逐渐饱和。厌氧条件下,吸附作用不明显;当反应时间达到24 h后,上覆水磷质量浓度保持不变,此时沉积物磷吸附达到饱和。高溶解氧水平对于控制底泥向上覆水体释放磷,维持水体较低总磷是必要的。温度为30℃,20℃和5℃3种条件下,当反应24 h后,三者均达到吸附平衡。因此,当上覆水的磷质量浓度较低时,高温条件下基质的磷释放速度会高于低温条件下的磷释放速度。研究结果旨在为正确认识、合理评估环境因素对湖泊水体磷的影响提供更为充分恰当的试验依据和理论解释。     

Nitrogen- versus phosphorus-limited growth and sources of nutrients for coral reef macroalgae

Recent investigations of nutrient-limited productivity in coral reef macroalgae have led to the conclusion that phosphorus, rather than nitrogen, is the primary limiting nutrient. In this study, comparison of the dissolved inorganic nitrogen:phosphorus ratio in the water column of Kaneohe Bay, Hawaii, with tissue nitrogen:phosphorus ratios in macroalgae from Kaneohe Bay suggested that nitrogen, rather than phosphorus, generally limits productivity in this system. Results of nutrient-enrichment experiments in a flow-through culture system indicated that inorganic nitrogen limited the growth rates of 8 out of 9 macroalgae species tested. In 6 of the species tested, specific growth rates of thalli cultured in unenriched seawater from the Kaneohe Bay water column were zero or negative after 12 d. These results suggest that, in order to persist in low-nutrient coral reef systems, some macroalgae require high rates of nutrient advection or access to benthic nutrient sources in addition to nutrients in the overlying water column. Nutrient concentrations in water samples collected from the microenvironments inhabited or created by macroalgae were compared to nutrient concentrations in the overlying water column. On protected reef flats, inorganic nitrogen concentrations within dense mats of Gracilaria salicornia and Kappaphycus alvarezii, and inorganic nitrogen and phosphate concentrations in sediment porewater near the rhizophytic algae Caulerpa racemosa and C. sertularioides were significantly higher than in the water column. The sediments associated with these mat-forming and rhizophytic species appear to function as localized nutrient sources, making sustained growth possible despite the oligotrophic water column. In wave-exposed habitats such as the Kaneohe Bay Barrier Reef flat, water motion is higher than at protected sites, sediment nutrient concentrations are low, and zones of high nutrient concentrations do not develop near or beneath macroalgae, including dense Sargassum echinocarpum canopies. Under these conditions, macroalgae evidently depend on rapid advection of low-nutrient water from the water column, rather than benthic nutrient sources, to sustain growth. Received: 1 December 1997 / Accepted: 9 July 1998     

Multiphase redistribution differences of polycyclic aromatic hydrocarbons (PAHs) between two successive sediment suspensions

Successive sediment suspensions often happen in estuary, yet little research has probed into the difference in the release behaviors of organic compounds among different suspensions. This study took polycyclic aromatic hydrocarbons (PAHs) as typical organic contaminants and investigated the release behaviors between two successive suspensions with a particle entrainment simulator (PES). Results showed that successive sediment suspensions lowered the concentration of dissolved PAHs in the overlying water via facilitating the re-adsorption of dissolved PAHs onto the suspended particles. Fast-release and slow-release periods of PAHs were successively observed in the both suspensions. The concentration changes of dissolved PAHs in the second suspension were generally similar with but hysteretic to those in the first suspension. More vigorous desorption and re-absorption of PAHs were induced in the second suspension. Successive sediment suspensions obviously decreased the concentrations of mineral composition and organic matters in the overlying water, which significantly affects multiphase distribution of PAHs.     

Inventories and Distribution of Radiocaesium in Arctic Marine Sediments: Influence of Biological and Physical Processes

Extensive surveys of sediment burdens of radiocaesium, specifically ¹³⁷Cs, and other radioactive contaminants in the Arctic during the 1990's, indicate that almost all anthropogenic radionuclides buried on continental shelves adjacent to Alaska are derived from global bomb fallout. the ¹³⁷Cs (half-life: 30.2y) activities observed in surface (0-4 cm) marine sediments however, vary widely, albeit much less than the expected current inventory resulting from bomb fallout at this latitude (∼100mBq cm^-2). This observed geographical variation provided the opportunity to evaluate physical and biological mechanisms that may affect caesium biogeochemistry on Arctic continental shelves. We investigated whether high biological productivity in portions of the Bering and Chukchi Seas is effective in removing dissolved radiocaesium from the water column, and whether biological production in overlying water affects total radiocaesium inventories in sediments. Based upon C/N ratios in the organic fraction of shallow sediments, we found no evidence that higher inventories or surface activities of radiocaesium are present in areas with higher deposition of particulate organic matter. Based upon stable carbon isotope ratios of organic matter in sediments, we found no evidence that terrestrial runoff contributes proportionally to higher surface activities, although terrestrial runoff may affect total inventories of the radionuclide. Radiocaesium content of surface sediments was significantly correlated with total organic carbon content of sediments and the proportion of sediments in the finest sediment fractions. Because high current flow can also be expected to influence distributions of those sedimentary parameters, we conclude that re-distribution of