The chemical character and burial of phosphorus in shallow coastal sediments in the northeastern Baltic Sea

The chemical composition and vertical distribution of sediment phosphorus (P) in shallow coastal sediments of the northeastern Baltic Sea (BS) were characterized by sequential extraction. Different P forms were related to chemical and physical properties of the sediments and the chemistry of pore water and near-bottom water. Sediment P composition varied among the sampling sites located in the Archipelago Sea (AS) and along the northern coast of the Gulf of Finland (GoF): the organic rich sites were high in organic P (OP), while apatite-P dominated in the area affected by sediment transportation. Although the near-bottom water was oxic, the sediments released P. Release of P was most pronounced at the site with high sediment OP and reduced conditions in the sediment-water interface, indicating that P had its origins in organic sources as well as in reducible iron (Fe) oxyhydroxides. The results suggest that even though these coastal areas are shallow enough to lack salinity stratification typical for the brackish BS, they are vulnerable to seasonal oxygen (O₂) depletion and P release because of their patchy bottom topography, which restricts mixing of water. Furthermore, coastal basins accumulate organic matter (OM) and OP, degradation of which further diminishes O₂ and creates the potential for P release from the sediment. In these conditions, an abundance of labile OP may cause marked efflux of P from sediment reserves in the long-term.     

Forms and distribution of inorganic phosphorus in sediments of two shallow eutrophic lakes in Florida

Physicochemical attributes were measured and aquatic macroinvertebrates were collected from six wetlands near Perth, Western Australia at three weekly intervals over a 13 month period from August 1988 to September 1989. The six wetlands encompassed a range of depths, pH, concuctivities, nutrient concentrations and colours. Temporal changes in the macroinvertebrate communities appeared to be related to seasonal changes in the physical and chemical characteristics of the wetlands. Community composition differed more between the less enriched wetlands then the higly enriched wetlands where communities were generally similar. High species richness was associated with seasonal drying. High macro invertebrate abundance appeared to be associated with the presence of either green algal or cyanobacterial blooms in the enriched wetlands. The highest macroinvertebrate biomass was recorded in wetlands with both cyanobacterial blooms and abundant macrophytes present.     

上覆水性质对沉积物吸附有机污染物能力的影响

采用正交实验法研究了温度、pH、离子强度和溶解性有机质(DOC)对沉积物吸附菲和五氯酚(PCP)能力的影响.结果表明,上覆水温度和pH对个别沉积物的吸附能力有显著影响,其他因素及交互作用对菲和PCP的吸附无显著影响.沉积物对菲的吸附能力随温度升高而降低,对PCP在中温(20℃)时最小.pH对菲的吸附无显著影响,PCP的吸附量随pH升高而降低.DOC升高微弱地降低了菲和PCP的吸附,离子强度升高使PCP的吸附有微弱升高.沉积物对有机污染物的吸附能力主要由沉积物和有机污染物性质决定,受上覆水性质影响较小.     

Phosphorus dynamics in shallow eutrophic lakes: an example from Zeekoevlei,South Africa

Zeekoevlei is the largest freshwater lake in South Africa and has been suffering from hyper-eutrophic conditions since last few decades. We have used total P (TP), dissolved phosphate (PO₄ ³⁻), organic P (OP), calcium (Ca) and iron (Fe) bound P fractions to investigate the relevant physical, chemical and biological processes responsible for sedimentation and retention of P and to study phosphorus (P) dynamics in this shallow lake. In addition, redox proxies (V/Cr and Th/U ratios) are used to study the prevailing redox conditions in sediments. Adsorption by CaCO₃ and planktonic assimilation of P are found to control P sedimentation in Zeekoevlei. Low concentration of the labile OP fraction in surface sediments restricts the release of P by bacterial remineralisation. Low molar Ca/P and Fe/P ratios indicate low P retention capacity of sediments, and P is most likely released by desorption from wind-induced resuspended sediments and mixing of pore water with the overlying water column. Handling editor: J. Saros     

Uranium sorption onto natural sediments within a small stream in central Japan

In this study, we surveyed the uranium (U) load in stream water within a humid forest in Japan, and clarified the fact that changes in U load depended on the amount of sediment accumulated behind dams constructed along the stream. To elucidate the relationship between U and the accumulated sediments, we conducted U sorption experiments in the laboratory using stream water and sampled sediments. The chemistry of the stream water was analyzed in the field for pH, electrical conductivity (EC), and temperature, as well as laboratory analyses via inductively coupled plasma mass spectrometry (ICP-MS). We determined the amount of organic material, amorphous material, and total U contents in the sediments. Following the sorption experiments, we analyzed the pH and U concentrations in experimental solutions and determined the distribution coefficients of U for the sediments. The logarithm value of the distribution coefficients of U for amorphous material shows a positive correlation with pH, while the logarithm value of the distribution coefficients of U for organic material is independent of pH (4.7–6.9). Although the logarithm value of the distribution coefficient of U for amorphous material was 0.1–0.5 units larger than the value for organic material, U was effectively removed from the stream water by sorption onto organic material (humic substances and decomposing leaves), because the amount of organic material exceeded that of amorphous material.     

Vertical distribution and chemical character of sediment phosphorus in two shallow estuaries in the Baltic Sea

The vertical distribution of various phosphorus (P) forms and their relation to physico-chemical properties of estuary sediment material were studied to better understand the potential release and burial of P. Core samples were taken from two dissimilar estuaries in the Baltic Sea: one in the Archipelago Sea (AS) and one in the Gulf of Finland (GoF). The P reserves were characterized by a sequential extraction procedure including the analysis of simultaneously dissolved elements in two extraction steps. The sediment material was also analysed for particle size distribution and total elements. In addition, several environmental variables were determined. The occurrence of the various forms of P varied with sediment depth among different sites. Reductant soluble, iron (Fe) bound P was the most dynamically changing P form in the sediment, while P bound to other metal oxides and apatite-P were the most stable fractions. High sedimentation rate was a dominating factor for sediment P burial. In addition, the content of organic matter, the amount of erosion-transported sorption components, and the oxygen (O₂) conditions in the near-bottom water were important determinants of the behaviour of sediment P. The results indicate that, over the long term, both estuaries have acted as sinks for deposited P and restricted the transport of P to the AS and the open GoF, thereby partly alleviating the eutrophication process.     

Mineralization of dissolved organic phosphorus from a shallow eutrophic lake

Release of soluble reactive phosphorus (SRP) from dissolved organic phosphorus (DOP), concentrated by reverse osmosis of water samples from Lough Neagh Northern Ireland, was measured in the presence of enzymes and cultures of lake water bacteria in a basal liquid medium adjusted to the pH of lake water (7.6). No hydrolysis of unfractionated DOP was observed in the presence of alkaline phosphatase but a combination of alkaline phosphatase and phosphodiesterase mineralized 14% of DOP in a 30 day incubation period at 15 °C. A similar amount of mineralization was attained by phytase. Phytase induced the same degree of mineralization in a range of DOP fractions varying from MW > 100 000 to c. 500. A mixed culture of lake water bacteria mineralized 12% of unfractionated DOP. Single cultures of lake water bacteria displayed low mineralizing activity (mean of 49 cultures = 5% DOP hydrolysed). Results indicate that DOP from Lough Neagh in the above molecular weight range is predominantly recalcitrant to bacterial mineralization under natural lake conditions.     

大型浅水富营养化湖泊中蓝藻水华形成机理的思考

湖泊富营养化依然是我国目前以及今后相当长一段时期内的重大水环境问题。研究蓝藻水华的形成机制 ,对于科学预测湖泊中蓝藻水华的产生 ,并采取相应措施减少其带来的影响具有重要的生态和环境意义。为探索富营养化湖泊中蓝藻水华形成机理 ,综述了目前对我国大型浅水湖泊蓝藻水华成因研究现状和对水华形成机理的一般认识。分析了导致蓝藻水华形成的化学、物理和生物等主要环境因素 ,论述了蓝藻 ,尤其是微囊藻成为水华优势种的可能原因。认为对水华的形成需要全面认识 ,营养盐浓度的升高可能仅是蓝藻水华形成、且人们可以加以控制的因素之一 ;在探索水华成因时 ,不能仅仅局限于夏季蓝藻水华发生时环境特征的研究与观察 ,而应该提前关注蓝藻的越冬生理生态特征、春季复苏的生态诱导因子及其阈值以及在复苏后 ,蓝藻如何在生长过程中形成群体 ,并逐步成为湖泊水生生态系统中的优势种乃至形成水华的过程。并需要对蓝藻越冬的生存对策、蓝藻群体的形成的条件、蓝藻在春季复苏的触发条件及其生态阈值、以及蓝藻在与其它藻类种群竞争中取胜的生理生化特征有足够的认识。蓝藻水华的“暴发”是表观现象 ,其前提还是藻类一定的生物量 ,且是一个逐渐形成的过程。根据生态学的基本理论和野外对水华形成过程的原位观测     

Nitrate uptake rate in anoxic profundal sediments from a eutrophic reservoir

There is renewed interest in the use of nitrate to treat the profundal zone of lakes to inhibit anaerobic biogeochemical processes that result in the degradation of bottom water quality (e.g., sediment phosphorus release, mercury methylation). In this study we used experimental sediment–water interface chambers to quantify the rate of sediment nitrate uptake (SNU) in profundal sediments from Lake Perris, a eutrophic raw water reservoir in Southern California. Deoxygenated chamber water was spiked with nitrate, and nitrate concentration was monitored over time under quiescent conditions, followed by mixed conditions with average water velocities of 1 cm/s. Key findings included: (1) SNU decreased with decreasing nitrate concentration, (2) SNU was higher under mixed versus quiescent conditions by nearly 50%, and (3) nitrate uptake as a function of nitrate concentration followed a conventional sediment oxygen demand model in which nitrate uptake was proportional to the square root of nitrate concentration. The probable mechanism for elevated SNU under mixed conditions was an increased diffusional concentration gradient combined with a decrease in the diffusional boundary layer at the sediment–water interface, both of which enhanced the flux of nitrate from overlaying water into sediment. Managers planning to implement lake nitrate addition should account for induced nitrate demand when determining dosing rates. For example, based on our modeling efforts from this data set, SNU in Lake Perris could range by an order of magnitude, from around 12 mg N/m²/d under quiescent, low nitrate conditions (0.1 mg N/l) to around 120 mg N/m²/d under mixed, high nitrate conditions (5 mg N/l). Handling editor: L. Naselli-Flores     

Spatial variation of phosphorus fractions in bottom sediments and the potential contributions to eutrophication in shallow lakes

Spatial variation of phosphorus fractions in bottom sediment, pore water and overlying water in three shallow eutrophic lakes, Nishiura, Kitaura and Sotonasakaura, Japan, and the contributions of the fractional P to mobilization of phosphorus from sediment were examined in this study. The vertical distributions of dissolved inorganic phosphorus (DIP) concentrations in overlying and pore water differed with lake and sampling site. In particular, DIP was high in pore water in the surface layer of the sediment for the middle to downlake areas of Lake Kitaura. DIP release flux calculated from a gradient of the concentrations at the sediment–water interface was high compared with other sites. The distribution of fractional P content in sediments was highly variable. The citrate–dithionite–bicarbonate–non-reactive phosphorus (CDB–NRP) fraction, in particular, differed greatly among the three lakes. According to correlation in the ratios between CDB–NRP and loss on ignition, sediments of these lakes were classified in three clusters. The CDB–NRP fraction was suggested to play a role in DIP release from sediment. The possibility of nitrate concentration playing a role in the control of DIP release was considered.     

Mineralization, pore water chemistry and phosphorus release from peaty sediments in the eutrophic Loosdrecht lakes, The Netherlands

SUMMARY. 1. Pore water chemistry in peaty sediment was monitored for a year at two representative locations of the eutrophic shallow Loosdrecht lakes. The Netherlands. Phosphorus fluxes over the sediment-water interface were calculated using measured concentration gradients in the pore water and compared to fluxes measured under laboratory conditions. Results were analysed with Redundancy Analysis to detect patterns of variation in pore water chemistry and in measured and calculated fluxes, that could be ascribed to environmental variables.
2. It was demonstrated that phosphorus fluxes measured in long-term laboratory incubations were not correlated to any of the pore water characteristics.
3. Initial phosphorus fluxes measured in sediment columns, which varied between −7.7 and 1330 μmol m⁻²: day⁻¹, were correlated significantly to the calculated phosphorus flux over the sediment-water interface.
4. The high correlation between calculated fluxes of ammonia, phosphorus and methane and measured initial flux of phosphorus, conclusively pointed to mineralization of organic matter as the driving force for phosphorus release from the sediment.
5. Redundancy Analysis demonstrated that the rates of mineralization and phosphorus release were only weakly related to temperature. They appeared to be especially stimulated by the autumnal decrease in temperature which was probably related to an extra input of organic matter.     

Mechanisms regulating abundance of submerged vegetation in shallow eutrophic lakes

Shallow eutrophic lakes tend to be either in a turbid state dominated by phytoplankton or in a clear-water state dominated by submerged macrovegetation. Recent studies suggest that the low water turbidity in the clear-water state is maintained through direct and indirect effects of the submerged vegetation. This study examined what mechanisms may cause a recession of the submerged vegetation in the clear-water state, and thereby a switch to the turbid state. The spatial distribution of submerged vegetation biomass was investigated in two shallow eutrophic lakes in the clear-water state in southern Sweden. Biomass of submerged vegetation was positively correlated with water depth and wave exposure, which also were mutually correlated, suggesting that mechanisms hampering submerged vegetation were strongest at shallow and/or sheltered locations. The growth of Myriophyllum spicatum, planted in the same substrate and at the same water depth, was compared between sheltered and wave exposed sites in two lakes. After 6 weeks the plants were significantly smaller at the sheltered sites, where periphyton production was about 5 times higher than at the exposed sites. Exclosure experiments were conducted to evaluate the effects of waterfowl grazing on macrophyte biomass. Potamogeton pectinatus growth was decreased by grazing, whereas M. spicatum was not affected. The effects were greater at a sheltered than at a wave-exposed site, and also negatively related to distance from the reed belt. These results suggest that competition from epiphytes and waterfowl grazing hamper the development of submerged vegetation at sheltered and/or shallow locations. An increased strength of these mechanisms may cause a recession of submerged vegetation in shallow eutrophic lakes in the clear-water state and thereby a switch to the turbid state. Received: 24 June 1996 / Accepted: 8 September 1996     

Development of a new aggregative index to assess potential effect of metals pollution in aquatic sediments

A new aggregative index called modified risk assessment code (mRAC) was developed based on heavy metal toxicity and fractionation in aquatic sediment. Results of the application of mRAC to assess metal pollution in surface sediment samples of Anzali international wetland revealed that the new index led to more precise results than those of other prevalent aggregative indexes, such as modified degree of contamination (mC_d) and ecological risk index (RI). Based on assessment by mRAC, sediments of the study area were at high or very high potential adverse effect levels, compared to using mC_d and RI where sediments were at a moderate or low potential adverse effect level. This is due to mRAC taking both metal toxicity and fractionation into account.     

湖北省若干浅水湖泊沉积物有机质与富营养化的关系

分析了湖北省月湖、龙阳湖、后官湖、梁子湖、牛山湖、保安湖、鲁湖等7个湖泊表层沉积物有机质、总氮与总磷的含量,并考察了其在月湖、龙阳湖沉积物中的垂直分布及月湖、龙阳湖与保安湖表层沉积物的颗粒组成,结果表明：位于城市与城郊的月湖与龙阳湖表层沉积物有机质含量较高,且表现出沿岸带较丰富的空间分布特征。在垂直及水平方向上,有机质与总氮和总磷含量均显著相关,颗粒组成与有机质和总氮含量亦显著相关。有机质富集应是促进城市湖泊富营养化的重要因素。     

Iron:phosphorus ratio in surface sediment as an indicator of phosphate release from aerobic sediments in shallow lakes

Analysis of Danish lakes showed that both mean winter and mean summer concentrations of lake water total phosphorus in the trophogenic zone correlated negatively with the total iron to total phosphorus ratio (Fe:P) in surface sediments. No correlation was found between the water total phosphorus concentration and either the sediment phosphorus concentration alone or with sediment calcium concentration. The increase in total phosphorus from winter to summer, which is partly a function of net internal P-loading, was lowest in lakes with high Fe:P ratios in the surface sediment.A study of aerobic sediments from fifteen lakes, selected as representative of Danish lakes with respect to the sediment Fe and phosphorus content, showed that the release of soluble reactive phosphorus was negatively correlated with the surface sediment Fe:P ratio. Analysis of phosphate adsorption properties of surface sediment from 12 lakes revealed that the capability of aerobic sediments to buffer phosphate concentration correlated with the Fe:P ratio while the maximum adsorption capacity correlated with total iron. Thus, the Fe:P ratio may provide a measure of free sorption sites for orthophosphate ions on iron hydroxyoxide surfaces.The results indicate that provided the Fe:P ratio is above 15 (by weight) it may be possible to control internal P-loading by keeping the surface sediment oxidized. Since the Fe:P ratio is easy to measure, it may be a useful tool in the management of shallow lakes.     

三峡水库香溪河库湾沉积物对磷的吸附特征研究

通过三峡水库香溪河库湾的3个采样点沉积物中磷的自然吸附实验和不同粒径下沉积物的胁迫吸附试验,研究了沉积物对磷的吸附特征。结果表明:上覆水中的磷浓度与沉积物中的总磷含量有很好的相关性,沉积物中的总磷含量对上覆水的水质有很大的影响;三点的临界平衡浓度为C1:0.188mg/L,C2:0.147mg/L,C3:0.188mg/L;各点增加的量即饱和吸附量不同(ΔQ1:268.16mg/kg,ΔQ2:57.96mg/kg,ΔQ3:267.27mg/kg),恰恰与三点的临界平衡浓度之间的关系一致;粒径对沉积物对磷的吸附量影响程度与沉积物理化参数也存在很大的关系;三个样点的吸附量,分别接近于1.5mg/g,0.8mg/g及1.4mg/g。结果还表明:最大吸附量大的地方,饱和吸附量不一定就大,二者之间不存在必然的关系;香溪河沉积物中的磷在现有条件下表现为“源”,不排除外在条件改变时转化为“汇”。如果最大吸附容量、饱和吸附容量及平衡浓度能够很好的与数学相结合,可为当地的环保部门管理香溪附近工厂提供科学依据。     

Influence of redox potential on phosphate-uptake by sediments in two sub-tropical eutrophic lakes

Biogeochemical reactions in shallow eutrophic lakes areaffected bythe changes in redox potential (Eh) as bottom sedimentsundergotemporal resuspension and settling. The stability of varioussediment P fractions and kinetics of P-uptake were evaluatedfortwo sub-tropical lakes (Lake Apopka and Lake Okeechobee,Florida)using sediment suspensions in closed systems maintained atvariousEh levels ranging from –235 to 555 mV. Redox potential hadminimal effect on the stability of NaOH-P (Fe-/Al-bound P plusmoderately resistant organic P) and HCl-P (Ca-/Mg-P) fractionsinLake Apopka sediments. Increases in ortho-P and NH₄Cl-P(loosely-bound P plus labile organic P) concentrations wereobserved in highly reduced (Eh=–225 mV) Apopkasediments.Phosphate solubility diagrams and mineral equilibriacalculationssuggest that P-uptake by Apopka bottom sediments at elevated Pconcentrations (ortho-P110 M) was due toformationof Ca-P compounds and/or co-precipitation of P withCaCO₃. Incontrast, the ortho-P concentrations for Lake Okeechobeebottomsediments increased exponentially with decreasing Eh. Thequantityof NaOH-P fractions for these sediments decreased withdecreasingEh, suggesting the release of Fe- and Mn-bound P intosolution.Phosphate-uptake by Okeechobee bottom sediments (pH 7.5,ambient)followed first order kinetics, yielding a rate constant (k)of 0.51±0.05 h^-1. Unlike that of Apopka, the mudsediments in Lake Okeechobee have strong affinity for P ineitheraerobic or anaerobic conditions. Results suggest that even incalcareous systems, Fe and Al, when present in highconcentrations(as in the case of Lake Okeechobee), are actively involved inregulating P-uptake and geochemistry.     

The influence of water quality and sediment geochemistry on the horizontal and vertical distribution of phosphorus and nitrogen in sediments of a large,shallow lake

Distinct horizontal water column concentration gradients of nutrients and chlorophyll a (Chl a) occur within large, shallow, eutrophic Lake Taihu, China. Concentrations are high in the north, where some of the major polluted tributaries enter the lake, and relatively low in the south, where macrophytes generally are abundant. It is not clear, however, whether these water column concentration gradients are similarly reflected in spatial heterogeneity of nutrient concentrations within the bottom sediments. The main objective of this study was therefore to test if horizontal and vertical variations in the phosphorus and nitrogen content in bottom sediments of Lake Taihu are significantly related to (1) horizontal variations in overlying water column nutrient concentrations and (2) other sediment geochemical constituents. We measured the concentration of total phosphorus (TP) and total nitrogen (TN) in surficial sediments (0–2 cm) and TP, TN and Chl a concentrations in water column samples, collected from 32 sites in 2005. In 2006 sediment, TP, TN, carbon, iron and manganese concentrations were measured vertically at 2 cm intervals, extending to a depth of approximately 20 cm, at an additional eight sites. Linear correlation analysis revealed that surficial sediment TP concentrations across the 32 stations were related significantly, though weakly, to annual mean water column concentrations of TP, TN as well as Chl a. Correlations of surficial sediment TN with water column variables were, however, not significant (P > 0.05). Amongst the geochemical variables tested, the vertical variability of sediment TP concentrations was most strongly related to sediment manganese and carbon concentrations. A multiple stepwise linear regression revealed that the combination of sediment manganese and carbon concentrations explained 91% of the horizontal variability in sediment TP concentrations and 65% of the vertical variability. Handling editor: Luigi Naselli-Flores     

Physicochemical and sorption properties of thermally-treated sediments with high organic matter content

Sediment samples with high organic carbon contents (22.04% and 8.46%) were collected and thermally-treated using a method analogous to biochar production. The obtained thermally-treated sediments (TTSs) showed a much higher degree of carbon capture in comparison to biochar derived from common biomass, indicating potential use of TTSs in soil amendment and carbon sequestration. Their sorption with organic contaminants was also investigated using sulfamethoxazole (SMX) as a model sorbate. SMX sorption increased greatly with pyrolytic temperature. Desorption ratio of the adsorbed SMX in TTSs generally decreased with increased pyrolytic temperature and with decreased solid-phase concentrations. The thermodynamic analysis showed that the higher entropy increase (positive ΔS) was well related with the decreased desorption ratio with increased solid-phase concentration for the original sediments. The fate-controlling effect of contaminants in TTS application for soil amendment should be evaluated combining sorption/desorption and sorption thermodynamic studies.