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1.
The Marl Slate, the English equivalent of the Kupferschiefer, has been studied with particular reference to the relationships between dolomitization and the origin of the metal sulphides. Dolomite occurs as: 1) discontinuous lenses of ferroan dolomicrite, 2) micronodules of finely crystalline dolospar in association with length-slow chalcedony and 3) discrete laminae of ferroan or non-ferroan dolospar. The ferroan dolomicrite has excess CaCO3, and is more abundant in the lower, sapropelic facies of the Marl Slate. It is considered to have formed by the penecontemporaneous alteration of calcium carbonate under hypersaline conditions. Small micronodules (typically about 0.3 mm in diameter) are also more abundant in the sapropelic Marl Slate. These frequently contain cores of length-slow chalcedony (quartzine) fibres and sometimes quartz megacrysts. Textural observations clearly indicate that this silica is of authigenic origin and the dolomite/chalcedony micronodules are interpreted as diagenetic replacements of a calcium sulphate mineral such as anhydrite. The discrete laminae of finely crystalline dolospar are often inter-laminated with calcite in the upper part of the Marl Slate. This dolomite is also calcium rich and represents a replacement, possibly of anhydrite, during a later phase of diagenesis. Metal sulphides occur in two distinct forms: as disseminated framboidal pyrite and as discrete lenses of pyrite, chalcopyrite, galena, sphalerite and rarer sulphides. The framboidal pyrite originated during early diagenesis by reaction of sulphide, produced by reduction of sulphate by organic material and micro-organisms, with iron also released in the reducing environment. The sulphide lenses are often in intimate association with dolospar, length-slow chalcedony and authigenic quartz megacrysts. This indicates that the lenses were produced during diagenesis by the reduction and replacement of calcium sulphate (anhydrite). Various sources, such as co-precipitation with dolomite precursors and the underlying Yellow Sands, may have supplied metals which were mobilized and transported by connate brines as diagenesis progressed. 相似文献
2.
《Applied Geochemistry》2002,17(9):1171-1181
Sediment cores were collected from 20 lakes from the Muskoka region of Ontario, Canada, to study vertical changes in trace metal concentrations with depth and the distribution of metals amongst humic material, amorphous and crystalline Fe and Mn oxides, insoluble organics/sulphides, and silicates. Based on their total concentrations, trace elements displayed different degrees of affinity for the organic fraction (represented by organic C) and the mineral fraction (represented by Al). Certain elements (Hg, As, Sb, Pb, Cd, and Zn) displayed a positive correlation with organic C, a negative correlation with Al, and enrichment in surface sediments (with enrichment factors ranging from 2 to 24). Detailed speciation studies revealed that these elements were associated mainly with humic material and to a lesser extent with oxides in surface sediments. Other elements (Al, Cr, Co, Fe, and Mn) displayed a negative correlation with organic C, a positive correlation with Al, and no consistent enrichment in their total concentration at the surface. The speciation study revealed that metals of the latter group were mainly associated with the silicate fraction in both surface and deep sediments. This study shows that relative affinities for organic and mineral fractions play an important role in the distribution of trace metals during burial and diagenesis, and hence in the shape of their vertical profiles. 相似文献
3.
The diagenesis in the organic-rich Cretaceous to Eocene Al Hisa Phosphorite Formation (AHP), Muwaqqar Chalk Marl Formation (MCM) and Umm Rijam Chert-Limestone Formation (URC) formations of Jordan can be linked directly to the fluctuating sedimentary environment of this shelf depositional system in the Middle to Late Eocene, and its influence on the composition of the deposited sediment and the early burial diagenetic environment. Most cementation was early, mostly within the first 10 m of burial, perhaps entirely within the first 100 m of burial. We propose that the siliceous cements are derived from biogenic silica, probably of diatoms, deposited in a shelf of enhanced productivity. Volumetrically, the most important processes were the redistribution of biogenic opal-A (diatoms) and calcite to form pervasive, layered and nodular cements. The formation of the silica and carbonate cements is closely linked through the effects their dissolution and precipitation have on pore fluid chemistry and pH. The chert beds have a biogenic silica origin, formed through replacement of diatoms and radiolaria by opal-CT, and subsequently by quartz. Calcite cement has carbonate derived from microbial diagenesis of organic matter and calcium derived from seawater. The Mg for early dolomite may have been generated by replacement of opal-CT by quartz, ore dissolution of unstable high Mg calcite bioclasts. The silica and carbonate diagenetic processes are both linked to microbial diagenesis of organic matter, and are intimately linked in both time and space, with pH possibly influencing whether a silica or a carbonate mineral precipitates. The paucity of metal cations capable of precipitating as sulphides is crucial to the creation of acidic pore water favourable to silica precipitation, either as opal-CT, chalcedony or quartz. The lack of clay minerals as a sink for the Mg required for opal-CT polymerisation is the principal factor responsible for the remarkably early silica cementation. All the diagenetic processes, with the probable exception of the opal-CT to quartz transition are early, almost certainly within the first 10 m of burial, possibly much less. A paragenetic sequence is presented here based on these two cores that should be tested against a wider core distribution to see whether this diagenetic history can be generalised throughout the basin. Warm bottom water temperatures probably led to silica diagenesis at much shallower burial depths than occurs in many other sedimentary basins. Silicified layers, in turn, commonly host fractures, suggesting that mechanical properties of the strata began to differentiate at a very early stage in the burial cycle. This has wide implications for processes linking diagenesis to deformation. 相似文献
4.
The effects of diagenesis on marine organic material have been compared to those on terrestrial organic material in three Australian oil exploration wells. n-Alkaae distributions obtained for limestones ranged from C15 to C25 with no odd-even predominance and showed little variation with depth. n-Alkane distributions obtained for shales ranged from C15 to C33 and frequently had a pronounced odd-even predominance. Differences in the rates of hydrocarbon diagenesis between different rock types may be due to variations in either clay mineral content or the nature of the parent organic material. The individual n-alkane distributions of the sediments are determined by source material, degree of diagenesis and lithofacies. 相似文献
5.
页岩粒度细小、岩石致密、微观非均质性显著,在成岩作用改造下发育形成页岩气储层,成岩作用的研究可以为优质页岩储层发育机理提供依据。以渝西地区綦江观音桥剖面、南川泉浅1井、南川三泉剖面、大足Z-203井等代表性剖面、钻孔为例,通过X射线衍射、氩离子抛光—场发射扫描电镜、能谱、岩石薄片/光片显微观察、有机地球化学测试、力学特征测试等手段,对储层成岩作用及其对储层力学脆性的影响展开系统研究。结果表明,研究区五峰组—龙马溪组页岩物质组分、岩石结构、力学性质存在层段性差异,成岩作用阶段介于晚成岩作用阶段至极低级变质作用阶段之间;储层主要成岩作用类型可以划分为压实作用等物理性成岩作用、矿物溶蚀作用等矿物相关化学性成岩作用和有机质生烃作用等有机质相关化学性成岩作用三类。研究区五峰组—龙马溪组底部存在部分脆性矿物高于80%的超高脆性矿物含量层段,碳质—硅质富层理页岩在特殊储层成岩作用的影响下形成大量自生微晶石英,构成以微晶石英+赋孔有机质为主的显微物相组合,兼具良好的力学脆性与储集能力,而其他层段缺乏持续演化不断形成微晶石英的物质基础。储层成岩作用发生的物质基础、岩石结构、类型、作用强度在层段间的差异,是储层脆性矿物与力学性质差异的关键影响因素,应纳入储层评价与优质储层机理研究的关注范畴。 相似文献
6.
Multiscale characterization of pyritized plant tissues in blueschist facies metamorphic rocks 总被引：2，自引：0，他引：2
Sylvain Bernard Karim Benzerara Olivier Beyssac 《Geochimica et cosmochimica acta》2010,74(17):5054-5068
Pyritized plant tissues with well-preserved morphology were studied in rocks from Vanoise (western Alps, France) that experienced high-pressure, low-temperature metamorphic conditions in the blueschist facies during the Alpine orogeny. Organic and inorganic phases composing these fossils were characterized down to the nanometer scale by Raman microspectroscopy, scanning transmission X-ray microscopy and transmission electron microscopy. The graphitic but disordered organic matter composing these fossils is chemically and structurally homogeneous and mostly contains aromatic functional groups. Its original chemistry remains undefined likely because it was significantly transformed by diagenetic processes and/or thermal degradation during metamorphism. Various mineral phases are closely associated with this organic matter, including sulphides such as pyrite and pyrrhotite, carbonates such as ankerite and calcite, and iron oxides. A tentative time sequence of formation of these diverse mineral phases relative to organic matter decay is proposed. The absence of traces of organic matter sulphurization, the pervasive pyritization of the vascular tissues and the presence of ankerite suggest that the depositional/diagenetic environment of these metasediments was likely rich in reactive iron. Fe-sulphides and ankerite likely precipitated early and might have promoted the preservation of the fossilized biological soft tissues by providing mechanical resistance to compaction during diagenesis and subsequent metamorphism. In contrast, iron oxides which form rims of 100-nm in thickness at the interface between organic matter and Fe-sulphides may result from metamorphic processes. This study illustrates that it may be possible in some instances to deconvolve metamorphic from diagenetic imprints and opens new avenues to better constrain processes that may allow the preservation of organic fossils during diagenesis and metamorphism. 相似文献
7.
The geochemistry of selenium associated with coal waste in the Elk River Valley,Canada 总被引：1，自引：0，他引：1
Selenium (Se) concentrations more than 12 times greater than the provincial freshwater quality guideline (2 µg/L) were detected in the Elk River downstream from the five open-pit coal mines in southeastern British Columbia's Elk River Valley. To identify possible sources of Se to the Elk River, samples from the coal-bearing Mist Mountain Formation were studied using X-ray diffraction, elemental and oxide analyses, sequential extractions and heavy liquid separation. Between 2.5 and 21.3% of the total Se in the five types of materials studied is water-soluble and 1.0 to 10.6% is associated with hydrous ferric and manganese oxides. Se associated with sulphides and organic material varies between 60 and 84% of the total Se and Se in the silicate structure varies from 5.9 to 24.7%. The ratio of sulphides to the total of organic carbon is well-correlated with the amount of Se in materials closely associated with coal seams containing less than 6 mg/kg of Se (r=0.916). This may suggest that the amount of organic matter present during deposition affects the amount of Se incorporated into sulphides. 相似文献
8.
《Applied Geochemistry》1998,13(3):349-358
Geochemical data from 4 cores taken in the Eastern Gotland Basin of the Central Baltic Sea (68 to 243 m water depth) show that depositional conditions for heavy metals in sediments were similar at all water depths prior to anthropogenic influxes. After the onset of industrialization, the deep anoxic parts of the basin expanded at irregular intervals and the <63 μm fractions of the sediments became characterized by high organic C and heavy-metal accumulation rates. The difference between the enrichment patterns in the basin and on the slope suggests that material enriched in organic matter (and associated trace elements) and in sulphides (and associated trace elements) is preferentially deposited in the basin. The composition of the sediments in the basin therefore reflects the effects of lateral transport of the sediment, which enriches organic C in the deepest part of the basin and of anoxia in the deep water of the basin, where metal sulphides are formed. Previous estimates of the timing of the onset of industrial pollution in the Central Baltic may have been in error because these new data suggest that this began in the Eastern Gotland Basin in about 1870. 相似文献
9.
10.
Graham Bird Paul A. Brewer Mark G. Macklin Mihaela Serban Dan Balteanu Basarab Driga 《Journal of Geochemical Exploration》2005,86(1):26-48
The Abrud–Arieş river system, western Romania, is subject to ongoing mining activity associated with Cu, Pb and Zn ore extraction. The catchment contains what is believed to be Europe's largest unutilized Au deposit at Roşia Montană that is planned to be exploited by open-cast mining techniques. The magnitude and environmental significance of metal (Cd, Cu, Pb, and Zn) concentrations in surface water and river channel sediment have been investigated along a 140 km reach of the Rivers Abrud and Arieş and 9 tributaries affected by mining. The speciation of sediment-bound metals was established using a 4-stage sequential extraction procedure (SEP) that identified four chemical phases: (1) exchangeable, (2) Fe/Mn oxides, (3) organic matter/sulphides and (4) residual. Peak solute and sediment-bound metal concentrations were found to occur in the River Abrud downstream of the EM Bucium mine and in mining-affected tributaries, with up to 71% of sites containing sediment metal concentrations in excess of Dutch intervention values. The River Arieş was found to be much less polluted than the River Abrud, with only Cu showing concentrations above guideline values, as a consequence of porphyry Cu mineralization in the catchment. The magnitude and spatial extent of metal pollution is influenced by local physico-chemical conditions and hydrological linkages between mining and local river systems. Sediment-bound Cd and Zn were found to be predominantly associated with the exchangeable phase of the sediment (9–74% and 6–65%, respectively), whilst Fe/Mn oxides (5–76%) and organic matter/sulphides (1–45%) generally accounted for a majority of Pb and Cu partitioning, respectively. Sites of environmentally significant sediment-metal pollution were identified in the Rivers Abrud and Arieş where exchangeable metal concentrations exceeded Dutch intervention values. The implications of metal contamination in the Arieş river basin to the proposed mining development at Roşia Montana are discussed in relation to other contaminated Romanian catchments and with the EU Water Framework Directive. 相似文献
11.
Various Fe–S minerals of the mackinawite–greigite–pyrite association, ubiquitous in biogenic remains from Jurassic mudstones, have been described in detail in an SEM–EDS study. Two diagenetic stages of Fe sulphide formation and preservation in the Jurassic organic skeletons are identified. In the first stage, pyrite formed as euhedra and framboids shortly after deposition, mainly in the interiors of the skeletons which still contained labile organic matter. The second stage of iron sulphide formation was related to the later stages of diagenesis, when the influence of the surrounding sediment was more dominant, although some organic matter was still present in the biogenic skeletons. A Fe-rich carbonate–aluminosilicate cement was then introduced between the earliest iron sulphides and later subsequently sulphidized, to form a metastable iron monosulphide of mackinawite composition and then greigite. 相似文献
12.
康滇古大陆裂谷的发生和演化造就了楚雄盆地,沉积出煤、铜、盐旋回与含矿建造和矿床组合.铜矿的生成(特别是改造富集)与煤(有机质)、盐(热卤水)密切相关.大姚—牟定式砂岩铜矿以其规模最大而具代表性.它的成矿作用的演化是从风化沉积作用到成岩作用、后生作用再到改造作用.作用的结果是分别产生含铜有机质沉积体、成岩矿层、后生矿层和改造富矿体.层状矿体赋存于砂岩浅紫交互带是氧化性流体与还原性流体相汇于斯而发生氧化—还原反应沉积成岩的结果.其金属硫化物的生成顺序与分带是遵循S、O、Fe、Cu热液体系中矿物共生组合规律的,随介质条件、四元素浓度的差异而变化. 相似文献
13.
Aleksander Jokic Elena Ponomarenko Darwin W Anderson 《Geochimica et cosmochimica acta》2003,67(14):2585-2597
X-ray absorption near-edge structure (XANES) and nuclear magnetic resonance (NMR) spectroscopy were used in combination to characterize organic carbon structures in a series of wetland soils in Saskatchewan, and XANES spectroscopy was also used to examine sulphur speciation in the soils. The organic C contents of most of the wetland soils are consistently higher by a factor of two to five times compared to adjacent well-drained soils. NMR analyses indicate that the organic matter in the wetland soils consists of predominantly aliphatic structures such as carbohydrates and long chain poly(methylene) units which are refractory structures found in plant waxes. The poly(methylene) structures have a significant capacity to sorb nonpolar organic molecules. The phenolic OH and carboxyl group content of the wetland soils studied is an additional significant factor in their sequestering ability for heavy metals or pesticides. Carbon XANES spectroscopy shows that the surface (∼10 nm) layer of particulate organic matter has a structure dominated by aromatic, carbohydrate and carboxylic acid-like material apparently derived from partially degraded lignin and cellulose polymers which are adsorbed onto clay minerals. The aliphatic structures remaining in this surface layer are probably recalcitrant (poly)methylene units. At a depth of ∼100 nm, the aliphatic content significantly increases suggesting the presence of more labile structures. The presence of these more labile aliphatic compounds may be due to slow decomposition rates in the wet, often cool environments present and to the protective action of the more refractory components in the surface ∼10 nm of the organic matter. Drying of the wetlands, either by draining or as a result of climate change, is likely to result in the rapid decomposition of these labile organic structures releasing carbon dioxide. Our data indicate that the preservation of the organic carbon compounds in these soils is a result of their presence as surface adsorbed layers on the soil mineral particles. The soils contain three different classes of sulphur compounds: reduced organic sulphur such as sulphides, low valent oxidized sulphur such as sulphoxides, and high valent oxidized sulphur such as sulphonate and sulphate. Of these, reduced sulphur species constitute between one-third and two-thirds of the total. Sulphonate structures comprise between a fifth and a third of the total. Sulphates exhibit a wide variation in content, and sulphoxides are either not detected or are present to a lesser extent (<5%). Drying of the wetlands would cause oxidation of sulphides to sulphates. 相似文献
14.
R. Raiswell 《Chemical Geology》1976,18(3):227-244
Carbonate concretions from the Jet Rock (Upper Lias, Lower Jurassic) of NE England grew in uncompacted sediment, close to the sediment surface. Microbiological activity created isolated microenvironments in which dissolved carbonate and sulphide species were produced more rapidly than they could be dispersed by diffusion, so establishing the localised supersaturation of calcite and metastable iron sulphides. Precipitation of these minerals in the microenvironment formed a single concretion.Mass-balance calculations demonstrate that at least two different microbiological processes participated in concretionary growth. The early growth stages had an unidentifiable microbiological source of carbonate which declined in importance relative to sulphate reduction as growth proceeded. It is suggested that the diffusion of dissolved organic material was important in sustaining microbiological activity.Mineralogical zonations in the concretions result from changes in the chemistry of the microenvironment due to variations in the rates of addition/removal Ca2+, Fe2+, HCO?3 and HS? by microbiological activity, the crystallization of authigenic minerals and diffusion between the microenvironment and surrounding pore waters. Such changes are of only local significance and the resulting mineralogical zonations in a concretion cannot be used to deduce successive stages of diagenesis in the whole sediment. 相似文献
15.
Spatial variation in salinity, pH, redox potential, and in the concentrations of dissolved Mn, Fe2+ and sulphides in pore water were investigated in a mangrove system in the state of São Paulo (Brazil). Total organic C (TOC), S, Fe and Mn were analyzed in the solid phase, along with acid volatile sulphide (AVS), density of roots and percentage of sand. Five zones, situated along the length of a 180 m transect were considered in the study. Four of these were colonized by different species of vascular plants (Spartina, Laguncularia, Avicennia and Rhizophora) and were denominated soils; the other was not colonized by vegetation, and was denominated sediment. The results indicated important differences between the physicochemical conditions of the pore water in the vegetated zones and the sediment. In the former, two geochemical environments were identified, based on soil depths. The upper 20 cm contained the largest quantity of roots, and the conditions were oxic (Eh > 350 mV) or suboxic (Eh: 100–350 mV), acidic, and with high concentrations of Fe and Mn in the pore water. Below this depth, the soil became anoxic, the concentration of sulphides (HS−) increased significantly and the concentrations of dissolved Fe and Mn decreased significantly. The total S and the AVS fraction increased with depth, while TOC concentrations decreased, indicating that the decreases in Fe and Mn were due to the precipitation of metal sulphides. However, clear differences among the vegetated zones were not observed. The sediment was always anoxic, but with low concentrations of sulphide in the interstitial water, and was neutral or slightly alkaline. As in the soils, the concentrations of sulphides and total S increased significantly with depth, indicating that the conditions favoured the synthesis and stability of metal sulphides. 相似文献
16.
A baseline study of trace metals in a coral reef sedimentary environment,Lakshadweep Archipelago 总被引：3，自引：1，他引：2
Anu Gopinath S. M. Nair N. C. Kumar K. V. Jayalakshmi D. Pamalal 《Environmental Earth Sciences》2010,59(6):1245-1266
Surficial and core samples collected from the sedimentary microenvironments of Lakshadweep Archipelago were analysed for their
trace metal contents. The synoptical relations in spatial distributions with respect to environmental conditions such as pH,
organic carbon and sediment texture were inter-correlated. Some of the metals exhibited good correlations with Fe/Mn, which
reflect their similarity in distribution rather than anthropogenic enrichment. Inter-relating the variations in metal—pH relationships
with metal—organic carbon, in general, those which exhibited positive correlations with pH, displayed negative interactions
with organic carbon content and vice versa. Comparatively, higher values of Fe in the mangrove area of one of the islands
highlight the possibility of precipitation of Fe as iron sulphides, which are common in mangrove ecosystem. Based on the contamination
factors for Pb, Zn and Cd, as well as the geo-accumulation index of Cd, it can be generalised that some of the islands remain
polluted with respect to these elements. An evaluation based on pollution load index shows that none of the islands surveyed
for this study posed a serious threat in trace metal pollution. Bray Curtis similarity index was computed to find out the
similarity among metals/islands, using non-transformed data of metal concentrations. Group linkage clustering technique was
used for drawing dendrograms to show the similarity among them. 相似文献
17.
18.
S. Oszczepalski 《Mineralium Deposita》1999,34(5-6):599-613
The Kupferschiefer ore series, between the Lower Permian (Rotliegendes) terrestrial redbeds/volcanics and the Upper Permian (Zechstein) marine sequence, is developed as dark-grey organic matter-rich and metal sulphide-containing deposits (reduced zone) and as red-stained organic matter-depleted and iron oxide-bearing sediments (oxidized zone?=?Rote Fäule). The transition zone from oxidized to reduced rocks occurs both vertically and horizontally. This zone is characterized by sparsely disseminated remnant copper sulphides within hematite-bearing sediments, replacements of copper sulphides by iron oxides and covellite, and oxide pseudomorphs after framboidal pyrite. These textural features and copper sulphide replacements after pyrite in reduced sediments imply that the main oxide/sulphide mineralization postdated formation of an early-diagenetic pyrite. Hematite-dominated sediments locally contain enrichments of gold and PGE. The Kupferschiefer mineralization resulted from upward and laterally flowing fluids which oxidized originally pyritiferous organic matter-rich sediments to form hematitic Rote Fäule areas, and which emplaced base and noble metals into reduced sediments. It is argued that long-lived and large-scale lateral fluid flow caused the cross-cutting relationships, expansion of the hematitic alteration front, redistribution of noble metals at the outer parts of oxidized areas, and the location of copper orebodies directly above and around oxidized and gold-bearing areas. The Rote Fäule may be a guide to favourable areas for both the Cu-Ag and new Au-Pt-Pd Kupferschiefer-type deposits. 相似文献
19.
《Applied Geochemistry》2002,17(3):225-243
Altered wallrocks of vein-type Pb–Zn–Sb mineralization, Siegerland district, Rheinisches Schiefergebirge, have been investigated by a combination of inorganic and organic geochemical methods, including major and trace element analysis, vitrinite reflectance measurements, C isotope and elemental analysis of kerogen. Alteration features of the siliciclastic pelitic-psammitic Lower Devonian wallrocks are increased K/Na ratios, significant desilicification and relative immobility of a number of elements, notably Al, Ti, Zr, Cr, V. Wallrock kerogens display elevated vitrinite reflectance values, decrease in H/C atomic ratios coupled with increase in S/C atomic ratios and heavier C isotope compositions, compared to the unaltered precursor sedimentary rocks. Interaction processes between the hydrothermal fluids and the respective wallrocks, related to injection of high-temperature silica-undersaturated solutions, are dominated by quartz dissolution coupled with sericitization reactions. Heat transfer due to fluid infiltration/convection and wallrock reactions caused fluid cooling, which promoted the sequential deposition of quartz and stibnite/sulphosalts within the vein systems. Hydrocarbons, detected in ore assemblages of Pb–Zn and Sb mineralization, were most probably derived from the Lower Devonian very low-grade (meta)sedimentary rocks. High maturity levels and pronounced, typical organic alteration patterns indicate that thermochemical SO2−4 reduction (TSR) played an important role in precipitation of metal sulphides. The present study demonstrates that a combination of inorganic and organic investigations on fluid–rock interaction processes is particularly useful for deciphering precipitation mechanisms of base metal sulphides. 相似文献
20.
A simulated sedimentary system, capable of being controlled and monitored for a considerable length of time without undue disturbance, has been assembled and applied to specific problems of the genesis of stratiform Pb‐Zn ore deposits. Results have been obtained relevant to: (i) the concentration of Pb and Zn from brines to underlying sediments; (ii) the behaviour of microorganisms in metal‐rich, highly saline environments; (iii) the precipitation diagenesis of calcium and magnesium carbonates; and (iv) the diagenesis of organic matter. The experiment has demonstrated the feasibility of simulating a complex sedimentary environment in the laboratory and has indicated the potential of such systems for the investigation of geobiological problems. 相似文献