Geochemical records of the sediments and their significance in Dongping Lake Area,the lower reach of Yellow River,North China

Dongping Lake area, located in the lower reaches of Yellow River, is an ideal place to study the changes of modern river and lake sedimentary environment. The sediment samples of Dawen River, Yellow River, and Dongping Lake were collected, and the major elements, trace elements and organic matter geochemical composition of the samples were analyzed. Cluster analysis, characteristic element ratio method and graphic method were used to explore the geochemical characteristics of sediments and their environmental implication. The results show that the contents of SiO_2, Na_2O, TiO_2 and Zr in sediments of Dawen River and Yellow River are relatively high, and the contents of iron and manganese oxides, organic matter, CaO, P_2O_5 and Sr in lake sediments are relatively high. That reveals the differences of sedimentary environments between the rivers and the lake. The contents of Sr and Zr in Dawen River are affected by the rapid migration of clastic materials in the upstream carbonate source area during the flood season; the δCe,ΣREE and REE's ratios in the sediments of the Yellow River reflect the influence of the Loess source; and the distribution of elements changes along the flow direction during the flood season. The characteristics of p H, element composition and LREE HREE fractionation of the lake sediments indicate that the sediment source is complex, and the lake environment is affected by the flood season. The study shows that the geochemical content and its variation characteristics of sediments effectively reveal the sedimentary environment, material composition and characteristics of flood season of rivers and the lake in the study area.     

Flood zone biogeochemistry of the Ob River middle course

The flood zone of the Ob River, the largest (in watershed area) river of the Arctic Ocean basin, is tens of km wide and, after the Amazon's Varzea, is the world's second largest flooding territory. To better understand the biogeochemistry of the Ob River and adjacent surface waters, we studied, in May and July 2014, the dissolved and colloidal organic carbon and trace metals in small rivers, lakes, and flooded water bodies connected and disconnected with the mainstream as well as the Ob River itself. All major and trace elements were distributed among two major categories depending on their pattern of dependence on the dissolved organic carbon (DOC) concentration. Dissolved inorganic carbon (DIC), Na, Mg, Ca, sulfate, Sr, Mo, Sb and U exhibited a general decrease in concentration with the increase of the [DOC]. The lowest concentration of these elements was observed in DOC-rich humic, acidic (4.9 ≤ pH ≤ 6.1) upland lakes fed by surrounding bogs. These elements marked the influence of underground feeding in July during summer baseflow, which was most visible in flood lakes in the Ob riparian zone and the Ob River itself. In May, the flood lakes were statistically similar to the Ob River. The elevated concentration of DOC (up to 60 mg/L) in the upland lakes was not correlated with groundwater-related elements, suggesting a lack of significant groundwater feeding in these lakes. In contrast, insoluble, usually low mobile elements (Al, Fe, other trivalent hydrolysates, Ti, Zr, Hf) and some metals (Cr, Zn, Ni, Pb) demonstrated a steady increase in concentration with increasing DOC, with the lowest values observed in the Ob River and the highest values observed in small tributaries and organic-rich upland lakes in July. It follows that these elements are limited by their main carriers – organic and organo-ferric colloids, rather than by the availability of the source, peat and mineral soil or plant litter. While for the majority of non-colloidal, groundwater-fed elements with high mobility (DIC, Na, Mg, Ca, K, Sr…) the small tributaries can be used as representatives of the Ob main stream, this is not the case for low mobility “insoluble” elements, such as Fe, Al, trivalent and tetravalent hydrolysates, and metal micronutrients (Cu, Zn, and Mn). The low soluble elements and divalent metals exhibited a much lower concentration in the river mainstream compared to that in the flood lakes, upland lakes and small rivers. This difference is significantly more pronounced in the baseflow in July compared to the spring flood in May. Presumably, autochthonous processes, such as the photo-oxidation and bio-oxidation of organo-ferric colloids and phytoplankton uptake are capable decreasing the concentration of these elements in the river mainstream.     

New assessment of organic mercury formation in highly polluted sediments in the Lenga estuary,Chile

Anomalously high levels of mercury in sediment in the Lenga estuary, Chile are comparable to the most contaminated sites previously reported elsewhere. Total mercury (Hg_total) concentrations range from 0.5 to 129 mg kg⁻¹ and organic mercury (Hg_org) from 11 to 53 μg kg⁻¹. The highest levels are in areas near the previous wastewater outfall of a chlo-alkali plant. The results show that the proportion of Hg_org/Hg_total in the sediment varies by more than two orders of magnitude (0.02–5.7%) according to the concentration of Hg_total. No correlation between the concentration of Hg_org and Hg_total was found. The lack of correlation does contrast with the findings of other authors in culture media. Our results indicate that even at very high concentrations of Hg_total and organic matter do not influence organic mercury formation in estuary sediments. The disparity in Hg_total and Hg_org concentrations also attests to environmental differences in the formation.     

Evaluation of temporal concentration profiles for ungauged rivers following pollution incidents

Abstract

In order to predict the impact of pollution incidents on rivers, it is necessary to predict the dispersion coefficient and the flow velocity corresponding to the discharge in the river of interest. This paper explores methods for doing this, particularly with a view to applications on ungauged rivers, i.e. those for which little hydraulic or morphometric data are available. An approach based on neural networks, trained on a wide-ranging database of optimized parameter values from tracer experiments and corresponding physical variables assembled for American and European rivers, is proposed. Tests using independent cases showed that the neural networks generally gave more reliable parameter estimates than a second-order polynomial regression approach. The quality of predictions of temporal concentration profiles was heavily influenced by the accuracy of the velocity prediction.

Citation Piotrowski, A. P., Napiorkowski, J. J., Rowinski, P. M. & Wallis, S. G. (2011) Evaluation of temporal concentration profiles for ungauged rivers following pollution incidents. Hydrol. Sci. J. 56(5), 883–894.     

Paleocene-Eocene potential source rocks in the Avengco Basin,Tibet: Organic geochemical characteristics and their implication for the paleoenvironment

The Avengco Basin is located in the western part of the Tibetan Plateau and is similar to the Nima Basin in the central part of the plateau and the Lunpola Basin in the eastern part in terms of sedimentary characteristics and tectonic settings, which are well known to provide a good source rock potential. However, the organic geochemical characteristics of the Paleocene-Eocene potential source rocks in the Avengco Basin have been under debate. Thirty-four marl and mudstone outcrop samples of the Niubao Formation in the Avengco Basin were collected and subjected to the following analyses: total organic carbon (TOC), Rock–Eval pyrolysis, stable carbon isotopes of kerogen, gas chromatography (GC) and gas chromatography–mass spectrometry (GC–MS). Here, we present the results indicating the organic matter of the upper Niubao Formation is mainly composed of Type II kerogen with a mixed source, which is dominated by algae. However, the lower Niubao Formation has the less oil-prone Type II–III kerogen, and the sources of the organic matter are mainly terrestrial plants with less plankton. In addition, the samples are thermally immature to marginally mature. The Niubao Formation was deposited in an anoxic–oxic environment which was brackish with an imperceptible stratified water column. The upper Niubao Formation has a medium to good hydrocarbon-generating potential. However, the lower Niubao Formation has a zero to poor hydrocarbon-generating potential.     

Stable C and N isotope record of short term changes in water level in lakes of different morphometry: Lake Anastazewo and Lake Skulskie,central Poland

We present the stable C isotope record of the changes within the past 20 yr in water level of two morphologically different lakes in central Poland. The aim was to explain the relationship between lake water level and the δ¹³C signature of bulk sedimentary organic matter (δ¹³C_TOC) and to assess the potential of δ¹³C_TOC as a paleolimnological proxy of lake level change. This was done by comparison of the fossil δ¹³C_TOC record with instrumental data for lake level change in a shallow and small lake as well as in one large and deep basin. In both lakes the water table varied greatly between 1980 and 2000 AD. The δ¹³C_TOC data were supplemented with δ¹⁵N and bulk geochemistry data, as well as paleoecological data. We show that δ¹³C_TOC reacted to short term and low amplitude fluctuation in water level, but the response was highly dependent on the morphometry of the lake. In the shallow and small basin, δ¹³C_TOC decreased along with lake level drop due to oxidation and greater input of organic matter from macrophytes colonizing the lake bottom. On the contrary, in the deep/large lake δ¹³C_TOC decreased with increasing water level due to enhanced delivery of soil-derived OM to the lake during highstands. Our results have broad paleolimnological implications as they show that δ¹³C_TOC cannot act as a universal paleohydrological proxy. Its interpretation for a particular lake can be ambiguous and must be supported with additional geochemical and paleocological information.     

Palynofacies and organic geochemistry studies of organic matter from a wetland system of southern Brazil influenced by different hydrological regimes in the Quaternary

The main goal of this study was to quantitatively and qualitatively characterize the sedimentary organic matter (OM) and demonstrate the usefulness of geochemistry and palynofacies analysis for obtaining paleoenvironmental data for the Holocene in southernmost Brazil. The results indicate that during the time interval from 10,586 cal yr BP to the present, the study area housed a wetland characterized by different hydrologic regimes. The basal peaty deposits correspond to a phase influenced mainly by the groundwater table, whereas the upper deposits composed of silty organic mud indicate fluvial influence related to river overflow events. In a similar manner, the TOC (total organic carbon) and TS (total sulfur) contents are higher in the basal portion of the profile, decreasing toward the top. These findings could be related to granulometry alterations that are linked to hydrologic regimes or anthropogenic interference in the landscape dynamics. Anomalous TS content observed in one of the samples might be due to an external source and perhaps related to the presence of thermal springs in the region. These types of areas have potential as a modern reference that can be applied in the reconstruction of past analogous environments such as coal deposits associated with fluvial paleoenvironments.     

Soil discrimination using diffuse reflectance Vis–NIR spectroscopy in a local toposequence

Vis–NIR spectroscopy is nowadays presented as a possible routine method for soil sample analysis. However, there is still no consensus on which is the best multivariate statistical method to use. We propose to use principal component analysis to complete the spectral data treatment. The soil samples came from a pedological cover made up of red–yellow Latosols: 88 samples of 11 soil profiles on four toposequences were collected; clay, organic matter, silica, iron, aluminum and titanium total contents were determined; the contents of goethite, hematite, gibbsite, and kaolinite were calculated. Diffuse reflectance Vis–NIR spectroscopy at wavelengths from 400 to 2400 nm combined with principal component analysis (PCA) was sufficiently sensitive to discriminate different Latosols. Wavelengths of 700 nm and 2200 to 2300 nm were influenced by content ratios of organic matter and iron oxides (700 nm), and kaolinite and gibbsite absorption (2200 and 2300 nm). The spectral responses were affected not only by the content of these constituents, but also by the composition of the minerals, so that the same class of Latosol may have different or similar spectral responses. The role of microaggregation is discussed.     

古海洋研究中的地球化学新指标

有机地球化学与微量元素地球化学古环境指标及其相关的同位素指标已成为追溯古全球变化与古海洋生物地球化学演化的有力工具。从古环境替代指标的示踪原理和应用的角度，综述了有孔虫碳同位素、有机地球化学整体指标、生物标志化合物、单体有机分子同位素、微量元素等在古海洋古环境研究中的应用及相关的研究动态与进展。指出古海洋研究正从以恢复古海洋的物理参数（温度、盐度、古洋流等）为主，向着揭示古水团演化、古生产力、古营养状况、碳贮库及碳循环等古生物地球化学演化过程方向纵深发展。     

Coupling Interactions between Electrokinetics and Bioremediation for Pyrene Removal from Soil under Polarity Reversal Conditions

This paper investigates the hybrid technology of electrokinetics (EK) coupled with bioremediation (Bio) in the removal of pyrene (PYR) in a soil matrix. Five different treatments were conducted to investigate the coupling interactions between EK and Bio on PYR degradation. A simulated removal curve was obtained by combining the degradation curves in EK‐ and Bio‐only experiments. The results show that the simulated curve fitted well with the actual degradation curve in electro‐bioremediation (EK‐Bio) experiments for the first 30 days of the experiment, while at later stages a discrepancy was found. This discrepancy was caused by adverse effects of low soil pH (3.6) near the anode on bacteria health during EK treatments. With polarity reversal (PR) to control the soil pH, the simulated curve fitted very well (r > 0.99) with the actual degradation curve during the whole treatment period. At the end of the experiment, PYR removal amounted to 63% with EK‐Bio treatments in PR electric fields, which was 1.7 times that of Bio‐only. Moreover, the bacteria counts under electric fields were more than that without EK. The spatial distributions of PYR degradation and bacterial counts were also investigated. The results show that they were both higher nearer the electrodes under PR electric fields.