Organic carbon deposition and phosphorus accumulation during Oceanic Anoxic Event 2 in Tarfaya, Morocco     

Haydon P. Mort  Thierry Adatte  Gerta Keller  David Bartels  Karl B. Fllmi  Philipp Steinmann  Zsolt Berner  E.H. Chellai 《Cretaceous Research》2008,29(5-6):1008

With a multi-proxy approach, an attempt was made to constrain productivity and bottom-water redox conditions and their effects on the phosphorus accumulation rate at the Mohammed Plage section on the Tarfaya coast, Morocco, during the Cenomanian-Turonian Anoxic Event (OAE 2). A distinct δ¹³C_org isotope excursion of +2.5‰ occurs close to the top of the section. The unusually abrupt shift of the isotope excursion and disappearance of several planktonic foraminiferal species (e.g. Rotalipora cushmani and Rotalipora greenhornensis) in this level suggests a hiatus of between 40–60 kyrs at the excursion onset. Nevertheless, it was possible to determine both the long-term environmental history as well as the processes that took place immediately prior to and during OAE 2. TOC% values increase gradually from the base of the section to the top (from 2.5% to 10%). This is interpreted as the consequence of a long-term eustatic sea-level rise and subsidence causing the encroachment of less oxic waters into the Tarfaya Basin. Similarly a reduction in the mineralogically constructed ‘detrital index’ can be explained by the decrease in the continental flux of terrigenous material due to a relative sea-level rise. A speciation of phosphorus in the upper part of the section, which spans the start and mid-stages of OAE 2, shows overall higher abundances of P_reactive mass accumulation rates before the isotope excursion onset and lower values during the plateau. Due to the probable short hiatus, the onset of the decrease in phosphorus content relative to the isotope excursion is uncertain, although the excursion plateau already contains lower concentrations. The C_org/P_total and V/Al ratios suggest that this reduction was mostly likely caused by a decrease in the available bottom oxygen content (probably as a result of higher productivity) and a corresponding fall in the phosphorus retention ability of the sediment. Productivity appears to have remained high during the isotope plateau possibly due to a combination of ocean-surface fertilisation via increased aridity (increased K/Al and Ti/Al ratios) and/or higher dissolved inorganic phosphorus content in the water column as a result of the decrease in sediment P retention. The evidence for decreased P-burial has been observed in many other palaeoenvironments during OAE 2. Tarfaya's unique upwelling paleosituation provides strong evidence that the nutrient recycling was a global phenomenon and therefore a critical factor in starting and sustaining OAE 2.  相似文献   

Evaluation of coal bed methane potential of coal seams of Sawang Colliery,Jharkhand, India     

Anil M. Pophare  Vinod A. Mendhe  A. Varade 《Journal of Earth System Science》2008,117(2):121-132

The coal seams of Sawang Colliery, East Bokaro Coalfields are bituminous to sub-bituminous in nature and categorized as high gaseous seams (degree II to degree III level). These seams have the potential for coal bed methane (CBM) and their maturity increases with increasing depth, as a result of enhanced pressure-temperature conditions in the underground. The vitrinite maceral group composition of the investigated coal seams ranges from 62.50–83.15%, whereas the inertinite content varies from 14.93–36.81%. The liptinite content varies from 0.66% to 3.09%. The maximum micro-pores are confined within the vitrinite group of macerals. The coal seams exhibit vitrinite reflectance values (Ro% calculated) from 0.94% (sample CG-97) to 1.21% (sample CG-119). Proximate analyses of the investigated coal samples reveal that the moisture content (M%) ranges from 1.28% to 2.98%, whereas, volatile matter (VM%) content is placed in the range of 27.01% to 33.86%. The ash content (A%) ranges from 10.92% to 30.01%. Fixed carbon (FC%) content varies from 41.53% to 55.93%. Fuel ratio variation shows a restricted range from 1.53 to 1.97. All the coal samples were found to be strongly caking and forming coke buttons. The present study is based on the adsorption isotherm experiments carried out under controlled P-T conditions for determination of actual gas adsorption capacity of the coal seams. This analysis shows that the maximum methane gas adsorbed in the coal sample CG-81 is 17 m³/t (Std. daf), at maximum pressure of 5.92 MPa and experimental temperature of 30°C. The calculated Langmuir regression parameters P_L and V_L range from 2.49 to 3.75 MPa and 22.94 to 26.88 m³/t (Std. daf), respectively.  相似文献   

Phosphorus transport in shallow groundwater in peri-urban Kampala, Uganda: results from field and laboratory measurements   总被引：1，自引：0，他引：1  

N. R. Kulabako  M. Nalubega  R. Thunvik 《Environmental Geology》2008,53(7):1535-1551

To understand Phosphorus (P) sources and transport processes in the subsurface in Bwaise III Parish, Kampala, P attenuation and adsorption capacities of soils were studied in situ and from laboratory measurements. Relationships between sorption parameters and soil matrix properties, rates and mechanism of the adsorption process and soil P fractions were also investigated. P was generally higher in the wet than the dry season, but for both seasons, the maximum was 5 mgP/l. P transport mechanisms appeared to be a combination of adsorption, precipitation, leaching from the soil media and by colloids with the latter two playing an important role in the wet season. The sorption process comprised two phases with the first stage rate constants being about fourfold those of the second stage. The Langmuir isotherm described the sorption data well (R ² ≥ 0.95) with the second soil layer exhibiting the highest sorption maximum (C _max) (average value 0.6 ± 0.17 mgP/gDW). The best prediction of C _max had organic carbon, Ca, available P and soil pH. Residual P consisting mostly of organics was the main fraction in all the layers followed by inorganic HCl-P and NaOH-P in the top and middle layers, respectively. Loosely bound P (NH₄Cl-P) was the least fraction (<0.4% of total P) in all layers indicating the high binding capacity of P by the soils. The study results suggest that P dynamics is related to Ca, Fe and organic carbon content of the soils.  相似文献   

Usefulness of geological,mineralogical, chemical and chemometric analytical techniques in exploitation and profitability studies of iron mines and their associated elements     

M. Dolores Petit-Dominguez  M. Isabel Rucandio  Almudena Galan-Saulnier  Rosario Garcia-Gimenez 《Journal of Geochemical Exploration》2008

Due to the high number of variables involved in mine profitability studies, it is often very difficult to establish connections among them in order to provide a blend of market saleable quality products. In this sense, analytical chemistry together with chemometry are essential and indispensable disciplines to tackle these studies. The aim of this work was to demonstrate the utility of these disciplines to carry out optimization studies of iron mines. For this purpose, one of the most important iron mines of the Iberian Peninsula was chosen, sited in the mountain range of Sierra Menera, near the location of Ojos Negros (Teruel, Spain). Geological, mineralogical and chemical composition of 148 samples was analyzed, corresponding to different depths of three drill holes (named TE1, TE2 and TE3). In particular, aspects concerning to chemical composition are very important, since the mean contents of certain elements, such as phosphorus, sodium and potassium, should be restricted to the established limits to prevent that companies can drive back the raw material if they do not fulfil the necessary requirements. On the other hand, the large number of analysed samples drove us to use a statistical processing of the data. Among other aspects, it provides a way to find possible connections among a high number of variables and classify samples into compositional groups sharing similar composition, in order to limit the mineralised area and to obtain enough information about the amount of those chemical elements associated to iron ores. Data obtained from all these analytical techniques were in good agreement and provide a methodology that can be of wide interest applied to different geological studies.  相似文献   

土壤酶对碘离子在土壤中吸附行为的影响   总被引：1，自引：0，他引：1  

吴世军  陈繁荣  程俊  杨永强  吕莹  康明亮 《地球化学》2008,37(1):37-44

以批式试验法研究了微生物、葡萄糖氧化酶、脲酶、纤维素酶及其催化底物葡萄糖、尿素和纤维素对Ⅰ-在土壤中吸附的影响,结果表明微生物能显著提高Ⅰ-吸附量,但葡萄糖氧化酶、脲酶、纤维素酶及葡萄糖、尿素和纤维素对Ⅰ-吸附并无促进作用.葡萄糖氧化酶及葡萄糖含量在小于100 mg/L时对Ⅰ-吸附无影响,1000 mg/L时与Ⅰ-呈竞争吸附;脲酶及尿素随浓度增大,对Ⅰ-吸附的抑制作用变得明显;1～1000 mg/L范围内,纤维素酶和纤维素对Ⅰ-吸附没有影响;但葡萄糖氧化酶和葡萄糖生成的中间产物可促进土壤对Ⅰ-的吸附.平衡液中溶解性有机碳(DOC)含量随时间增加而逐渐降低,有机质浓度越大,降低趋势越明显.  相似文献   

沸石强化过滤的中试及生产性试验研究   总被引：2，自引：0，他引：2  

丁磊  王萍 《矿物学报》2008,28(3)

对新型水处理材料沸石强化常规给水处理工艺进行了中试和生产性试验,并与石英砂滤料做了对比.中试结果表明粒径为0.80-1.20mm沸石对浊度、氨氮、有机物都表现出良好的去除效果,过滤时的水头损失、反冲洗强度明显小于石英砂,不仅能满足反冲洗要求,还可节省反冲洗水量,降低运行成本.在生产性试验条件下,沸石对浊度、氨氮、耗氧量的去除率分别为95%、83%和39%.因此,在当前水源水遭到污染的情况下,用沸石替代石英砂滤料可明显改善水质,在不增加处理构筑物的情况下,对给水处理工艺可起到强化作用  相似文献   

污水-海水混合过程中磷转移的动力学   总被引：5，自引：0，他引：5       下载免费PDF全文

陈松  林汝健  廖文卓 《海洋与湖沼》1993,24(1):59-64

模拟研究厦门市污水排海时污水-海水混合过程中磷含量和形态的变化,及其在海水-颗粒物界面交换的动力学过程;提供转移模式,确定转移速率,进行磷的容量校正,为厦门西海域环境容量估算和水质控制提供定量参数和理论依据。  相似文献   

钛型吸附剂的表面特性     

谢式南  王俊鹤  周英兰  孙爱平 《中国海洋大学学报(自然科学版)》1990,(3)

用自装的BET容量法装置测定了几种粒状钛型吸附剂的比表面及其孔径分布。测定是在常温减压下进行的。结果表明:钛型吸附剂在加铀海水中的吸铀量与样品的比表面及孔径分布有一定的内在联系。这种表面性质的研究对吸附剂的筛选有重要的指导意义。  相似文献   

Study of Adsorption Isotherm Curves of Amino Acids on the Kaolinite     

刘效兰  张正斌 《海洋通报(英文版)》2002,4(1):52-60

This paper studies the adsorption isotherm curves of four amino acids (glyucine,aspartic acid,glutamic acid and lysine)and the effects of existences of different concentrations of Cu(Ⅱ) on them.Both the adsorption isotherm of the amino acids on the kaolinite and that when the copper ion Cu(Ⅱ） exists belong to the Langmuir type.The slopes of these adsorption isotherm increase with the increasing concentrations of Cu(Ⅱ） added.It can be explained in terms of formation of the type(Ⅰ） ternary surface complexes in these systems.The regular pattern of the effects of copper ion Cu(Ⅱ) on the adsorption isotherm of amino acids on the kaolinite is identical with that of its effects on the exchange and adsorption percentage E(%)-pH on the kaolinite in the same system.  相似文献   

砷酸根的液—固界面交换吸附研究——pH和Ca(Ⅱ)的影响     

赵卫红  张正斌 《中国海洋大学学报(自然科学版)》1997,(2)

研究ｐＨ和Ｃａ（Ⅱ）对砷酸根在海水与ＮａＣｌ介质中对水合氧化物和粘土矿物上交换吸附的影响：（１）在酸性条件下和海水及ＮａＣｌ介质中，砷酸根在针铁矿上的交换率Ｅ（％）—ｐＨ曲线呈平顶峰型、在δ－ＭｎＯ呈峰型、在粘土上分别呈双峰型和肩峰型。这是砷酸根存在多种形式与固体表面发生离子／配位子交换以及介质中阴离子竞争交换吸附共同作用的结果。（２）在碱性条件下的海水介质中，砷酸根与水合氧化物和粘土矿物的Ｅ（％）—ｐＨ曲线都呈Ｖ型，这是因为生成了具有一定结构的液—固界面三元络合物之故。（３）在ＮａＣｌ介质中，Ｃａ加入起促进作用，再次证明液—固界面三元络合物生成机理与Ｖ型曲线的内在关系  相似文献