根际环境锌镉镍的形态变化与植物有效性   总被引：1，自引：1，他引：1  

孙丽娜李玉双  李昕馨孙铁珩 《岩矿测试》2007,26(4):257-263

以抚顺西露天采场60平盘5种修复植物根际与非根际土为研究对象，运用顺序提取实验和数理统计分析方法研究了根际与非根际土中Zn、Cd、Ni的形态分布与植物有效性。结果表明，Zn、Ni在根际与非根际土中主要以硫化物态存在；而Cd在非根际土中以硫化物态为主，在根际土中以可交换态和松、紧有机态为主。与Ni相比，非根际土中Zn的紧有机态、氧化物态和Cd的紧有机态、氧化物态、可交换态比例明显偏大；与非根际土相比，根际土中Zn的铁锰氧化物态和硫化物态含量增加，碳酸盐态含量降低，松有机态、紧有机态和可交换态Zn在不同植物根际变化不同。Cd的硫化物态降低，可交换态、松有机态、碳酸盐态、氧化物态和紧有机态含量在不同植物根际变化不同。Ni的紧有机态显著增加，可交换态、碳酸盐态和硫化物态明显降低，松有机态在不同植物根际变化不同；根际Cd的碳酸盐态增加和氧化物态降低有利于植物Cd的吸收；碳酸盐态Zn的减少可促进植物Zn的增高。  相似文献   

样品处理与保存方法对表层沉积物中金属形态分析的影响   总被引：1，自引：0，他引：1  

王晓丽  李鱼  王婷  杜显元  李绪谦 《吉林大学学报(地球科学版)》2008,38(2):299-304

利用改进的Tessier连续萃取法研究了冷藏、冷冻、冻干、烘干和风干等样品处理与保存方法对表层沉积物中金属形态的影响。结果表明：各样品处理与保存过程对沉积物中Fe、Mn、Cu、Zn及Pb的形态均具有不同程度的影响,其中Fe的形态受其影响最小（<3.3%）,Mn的形态受其影响最大（最高可达10.2%）;冻干对各金属形态的影响最小（<4.6%）;烘干和风干对重金属Cu、Zn和Pb的可交换态（Ⅰ+Ⅱ）和非残渣态（Ⅰ-Ⅴ）分布影响较大,而冷藏、冷冻和冻干的影响相对较小。因此,综合考虑重金属的形态分布及其生物可利用性,冻干是较理想的沉积物样品处理与保存方法。  相似文献   

The role of iron and sulfur in the visual appearance of lake sediment varves     

Veronika Gälman  Johan Rydberg  Andrei Shchukarev  Staffan Sjöberg  Antonio Martínez-Cortizas  Richard Bindler  Ingemar Renberg 《Journal of Paleolimnology》2009,42(1):141-153

Easily discernible sediment varves (annual laminations) may be formed in temperate zone lakes, and reflect seasonal changes in the composition of the accumulating material derived from the lake and its catchment (minerogenic and organic material). The appearance of varves may also be influenced by chemical processes. We assessed the role of iron (Fe) and sulfur (S) in the appearance of varves in sediments from Lake Nylandssjön in northern Sweden. We surveyed Fe in the lake water and established whether there is internal transport of Fe within the sediment. We used a unique collection of seven stored freeze cores of varved sediment from the lake, collected from 1979 to 2004. This suite of cores made it possible to follow long-term changes in Fe and S in the sediment caused by processes that occur in the lake bottom when the sediment is ageing. We compared Fe and S concentrations using X-ray fluorescence spectroscopy (XRF) in specific years in the different cores. No diagenetic front was found in the sediment and the data do not suggest that there is substantial vertical transport of Fe and S in the sediment. We also modeled Fe and S based on thermodynamic, limnological, and sediment data from the lake. The model was limited to the five components H⁺, e^?, Fe³⁺, SO₄ ^2?, H₂CO₃ and included the formation of solid phases such as Fe(OH)₃ (amorphous), FeOOH (aged, microcrystalline), FeS and FeCO₃. Modeling showed that there are pe (redox) ranges within which either FeS or Fe(OH)₃/FeOOH is the only solid phase present and there are pe ranges within which the two solid phases co-exist, which supports the hypothesis that blackish and grey-brownish layers that occur in the varves were formed at the time of deposition. This creates new possibilities for deciphering high-temporal-resolution environmental information from varves.  相似文献   

Experimental Study of Gold and Platinum Solubility in a Complex Fluid under Hydrothermal Conditions   总被引：2，自引：0，他引：2  

G. G. LIKHOIDOV  L. P. PLYUSNINA  J. A. SCHEKA  T. B. APHANAS EVA 《Resource Geology》2000,50(2):83-92

Abstract: The solubility of gold was studied in water and aqueous NaCl (1– 5 m) solutions under oxygen and sulfur buffered conditions between 300–500C at a constant pressure 1 kb. Two buffer assemblages HMP and PPM were used. Analysis of the scatter in measured values in log m_Au–m_NaCl–T frame fixed linear dependence between log m_Au and T at any studied iso‐pleth (m_NaCl) in the form of log m_Au = a. T(C) + b. Coefficients of the equation were calculated for water and NaCl (1, 3, 5 m) solutions. The maximum solubility characterizes the NaCl‐free system in the presence of HMP. In the case, Au solubility increases from (log m_Au) –6. 72 to –5. 04 at 300 and 500C, respectively. In the presence of PPM, maximum of Au solubility was obtained for the 5 mNaCl solution. In a similar manner solubility rises from –6. 54 to –5. 77 at 300 and 500C, accordingly. In studied f_O2/f_S2 area the behavior of Au solubility testified that: (i) – a composite interaction between chloride and hydrosulfide speciation of gold affects its total solubility; (ii) – in addition of NaCl up to about 1. 5 m the solubility decreases, more pronounced in the presence of HMP; (iii) – the contribution of chloride in total Au solubility is more for PPM despite of lower f_O2value, than for HMP. The solubility of platinum was studied in the Pt–Cl–S–H₂O system between 300 and 500C, 1 kb. PPM solid buffer controlled oxidation state, pH and sulfur activity of solutions (H₂O, 1 mNaCl and 0. 1 mHCl). Under the conditions, PtS precipitated from the solutions with increasing temperature and acidity. The PtS solubility in the 0. 1 m_HCl solutions lowers slightly in the range of 300–500C from –5. 30 to –5. 60 (in log m_Pt) that is typical to the hydrosulfide species. It was deduced that reducing media, regulated by the PPM assemblage, suppress activity of chloride species of Pt. More oxidizing conditions were modeled in runs using mixtures of Mn(II), Mn(III) and Mn(IV) oxides to buffer the aqueous‐chloride solutions between 300 and 500C, 1 kb. It was found that MnO tends to oxidize at T below 400C forming intermediate Mn‐hydroxides (β–MnOOH, Mn (OH)₂ and Mn₂(OH)₃Cl). These phases are metastable and transfer to Mn₃O₄ with increasing duration. Generation of the Mn‐hydroxides leads to a change of physical‐chemical parameters of the solutions, such as water activity, pH and Eh. The last results in abrupt increase in the noble metals dissolution. At stable existence of only Mn₃O₄, the solubility of both Pt and Au lowers to equilibrium values. Essential catalysis effect of Pt on intensity and rate of Mn(II) oxidation was found. The dominant role of chloride of Pt and Au was defined under most oxidized conditions, specified by Mn₂O₃–MnO₂ buffer. So at 400C, dissolved Au (log m_Au) increases from –4. 40 in water to –1. 00 in 0. 1 m_HCl, and ones of Pt (log m_Pt) from –4. 80 to –2. 90 accordingly. Thus, mixing of hydrosulfide and chloride solutions, as well as transformation of the systems to the stable state act upon total solubility of the noble metals.  相似文献   

Secondary geochemical dispersion in the Precambrian auriferous Hutti-Maski schist belt, Raichur district, Karnataka, India. Part I: anomalies of As, Sb, Hg and Bi in soil and groundwater     

N. R. Sahoo  H. S. Pandalai   《Journal of Geochemical Exploration》2000,71(3):353

The nature of secondary geochemical dispersion of As, Sb, Hg and Bi in soil and ground water of the semi-arid, tropical, Archaean, auriferous, Hutti-Maski greenstone belt has been investigated for identification of appropriate geochemical techniques for Au exploration in similar terrains.Results indicate that the <180 μm size-fraction of C-horizon soil is an appropriate sampling medium for delineating pedogeochemical anomalies of As, Sb, Hg and Bi related to gold mineralisation. These pedogeochemical anomalies along with anomalous values of alkalinity, chloride, sulphate, As and Sb in groundwater are controlled significantly by primary mineralisation located along shear zones in the greenstone belt. Arsenic anomalies in soil are broad, whereas, those of Sb and Bi are restricted to narrow zones directly over mineralised areas. In contrast, Hg anomalies around known mineralised areas are irregular and do not clearly demarcate the mineralised areas. The study indicates that anomalies of As, Sb and Hg in soil are principally hydromorphic, whereas those of Bi are clastic.The study recommends use of groundwater sampling at 2–3 km spacing with routine analysis of chloride, sulphate and alkalinity along with As and Sb in the first phase. This may be followed up with sampling of C-horizon of soils on a 1 km square grid for As-anomalies. Arsenic-anomalous areas may be sampled for As, Sb, Hg and Bi on a 500 m square grid for detailed exploration.  相似文献   

湘西表生环境中的砷及其生态健康效应   总被引：2，自引：0，他引：2  

卢新卫  王五一  解庆林  马东升 《地质科技情报》2000,19(4):79-82

湘西是金、砷、锑、汞等有色金属的重要成矿带,区域地层微量元素地球化学研究表明,湘西所出露的地层均显著富集砷,是砷的高区域地球化学异常区,元素存在相态的实验进一步表明,新元古界至寒武系中的砷以易迁移形式为主,母岩的这一性质决定了其风化土壤中的砷的含量较高,土壤砷的高背景特征受人为采矿活动的影响,局部地区呈现高异常,土壤、水体砷的高异常已影响到居民的身体健康。  相似文献   

Zinc speciation in the Northeastern Atlantic Ocean     

Michael J. Ellwood  Constant M. G. Van den Berg 《Marine Chemistry》2000,68(4)

Measurements of zinc and zinc complexation by natural organic ligands in the northeastern part of the Atlantic Ocean were made using cathodic stripping voltammetry with ligand competition. Total zinc concentrations ranged from 0.3 nM in surface waters to 2 nM at 2000 m for open-ocean waters, whilst nearer the English coast, zinc concentrations reached 1.5 nM in the upper water column. In open-ocean waters zinc speciation was dominated by complexation to a natural organic ligand with conditional stability constant (log K_ZnL′) ranging between 10.0 and 10.5 and with ligand concentrations ranging between 0.4 and 2.5 nM. The ligand was found to be uniformly distributed throughout the water column even though zinc concentrations increased with depth. Organic ligand concentrations measured in this study are similar to those published for the North Pacific. However the log K_ZnL′ values for the North Atlantic are almost and order of magnitude lower than those reported by Bruland [Bruland, K.W., 1989. Complexation of zinc by natural organic-ligands in the central North Pacific. Limnol. Oceanogr., 34, 269–285.] using anodic stripping voltammetry for the North Pacific. Free zinc ion concentrations were low in open-ocean waters (6–20 pM) but are not low enough to limit growth of a typical oceanic species of phytoplankton.  相似文献   

生物迁移思想的起源与发展   总被引：3，自引：0，他引：3  

徐炳川 《地质力学学报》1995,1(3):89-96

生物迁移命题是由达尔文(1859)提出来的。他在《物种起源)一书中认为,一个物种只能有一个起源中心;在条件允许的前提下,它会从这个中心迁移到力所能及的地区。然而,当布克曼(1922)的"迁移炮弹"理论问世之后,迁移研究几乎陷于停顿状态差不多50年。李四光是在"迁移炮弹"阴影下,依然坚持迁移观点的少数科学家之一。越来越多的事实证明了达尔文迁移思想的强大生命力。屡见不鲜的化石"穿时"现象和时代差异,大量的生物地理新资料,使人们从不可知论的桎梏中逐渐解脱出来。特别是80年代以来,由于地壳运动理论研究的新需求,以及大陆漂移和海水进退规程研究的新进展,掀起了重新认识迁移的高潮。作者依据自己的积累和前人的研究成果认为,迁移的研究方法可概括为:最低层位的地理追索方法、演化程序的地理追索方法和相应环境的追索方法。迁移如同演化,在达尔文力的全弥漫作用(All pervadins action)下时刻在进行着。迁移与其说是生物自身的一种能力,倒不如说是环境给予的一种机会。迁移造就并维系着丰富多彩的自然生态系统。迁移研究必将发展而形成一门新的学科--古生物迁移学(Palaeobiomigratology)。生物迁移思想是与地质力学的诞生和发展共存的。李四光(1927,1928)在研究海水进退规程时,曾列举了伴随海水南北方向的运动,生物作相应迁移的许多事实。生物迁移和海水运动,是性质完全不同的两种运动,其间必然存在着一个联系两者的中间环节;这个环节被李四光(1962)暗示为气候的变化,或两者共同导源于地球自转的不均衡。   相似文献   

Relations between free copper and salinity, dissolved and particulate organic carbon in the Oosterschelde and Westerschelde, Netherlands     

L. J. A. Gerringa  H. Hummel  T. C. W. Moerdijk-Poortvliet 《Journal of Sea Research》1998,40(3-4)

In a previous investigation, relatively simple relations were found to estimate free Cu, and hence a good approximation of bio-available Cu, at two sites in estuarine waters of the Dutch Oosterschelde and Westerschelde. In the present study, these relations are validated for the remainder of the two sea arms. In the Westerschelde the relation between the concentration of a dissolved organic ligand (K=10¹³), DOC (dissolved organic carbon) and salinity is valid in a range of salinities at least from 10 up to 25 to 30. This ligand group is primarily riverine and partly estuarine. It is, as far as we know, the strongest ligand for Cu, and its concentration dominantly affects the free Cu ion concentrations, which are around 50 fM. At high salinities, dilution and mineralisation diminish the riverine member of the ligand group too much and the relation with salinity and DOC is no longer valid. In the Oosterschelde the relations between POC (particulate organic carbon) and particulate Cu and between POC and the ratio of particulate and dissolved Cu are valid for the western, central and eastern compartments. Since equilibrium was assumed to exist between dissolved and particulate Cu, free Cu can be calculated from POC and particulate Cu concentrations. Due to the large adsorption capacity of POC, the Oosterschelde is with respect to Cu a very well-buffered system with [Cu²⁺] of 20 fM.  相似文献   

Succession,palaeoecology, evolution,and speciation of Pennsylvanian non‐marine bivalves,Northern Appalachian Basin,USA     

R. M. C. Eagar  E. S. Belt 《Geological Journal》2003,38(2):109-143

Seventeen horizons of non‐marine bivalves are described within the Appalachian succession from the base of the Pottsville Group of Westphalian A‐B age to the Uniontown coal of Stephanian C age at the top of the Carboniferous System. A new highly variable fauna of Anthraconaia from the roof shales of the Upper Freeport coal near Kempton, west Maryland, dates from late Westphalian D or very early Cantabrian time, on the evidence of non‐marine shells and megafloras. Below this horizon, the Appalachian sequence reveals zones of Anthraconauta phillipsii and Anthraconauta tenuis in the same order as in Britain, whereas faunas of Anthraconaia of these zones are less common and differ from those of Britain. In all horizons above the Upper Freeport coal all non‐marine bivalve faunas consist of stages in the sequences of two natural species, the groups of Anthraconaia prolifera and Anthraconaia puella‐saravana. The first shows evidence of having lived in well‐oxygenated, probably shallow, fresh water conditions of relatively wide extent. The second group lived preferentially in a plant‐rich environment of relatively stagnant fresh water. Both groups are found in horizons associated with coal seams and may be seen together in the same habitats, but diagrams of variation (pictographs) suggest that there was no interbreeding between the two groups in either the Northern Appalachians or in southern Germany where the species split was first recognized. In the northern Spanish coalfields of Guardo‐Valderrueda and Central Asturia, facies evidence suggests how an initial split may have taken place in the same morphological directions and into the same palaeoenvironments as the later split into two species. Appalachian deposition was generally slow and intermittent with frequent palaeosols. There is also evidence of erosion and of small palaeontological breaks in the sequence, especially near the eastern edge of the Northern Appalachian Basin in western Maryland. The amount of accumulated sediment was less than one‐tenth of that of western Europe when basin centre deposition is compared. We found no evidence of a major palaeontological break representing Westphalian D strata overlain by Stephanian C strata. We figure non‐marine bivalve faunas of Stephanian B age in association with the Pittsburgh and the Little Pittsburgh coals. Two new species of non‐marine bivalves are described: Anthraconaia anthraconautiformis sp. nov. and Anthraconaia extrema sp. nov. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献