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1.
 The properties of soils on previously dated sand dunes from Robe to Naracoorte in South Australia were examined. In these areas younger sand dunes are composed of fresh sand, but older sand dunes are composed of calcarenited sand. The soils on the sand dunes developed successionally by the age of sand dunes. The soil properties of these sand dunes differ depending on the ages of the sand dunes. The properties of sand particles in soils are as follows: (1) On the sand dunes of 4300 years B.P., A/C profile developed (Rendzina). On the sand dunes older than 125 000 years B.P. and on the plateau of Tertiary limestone, soil profiles of A1/AB/B/C on the sand dunes of 83 000 years B.P. and A1/A3/B1/B2/C (Terra rossa) are well developed. (2) Within the sand of A/C horizons of the sand dunes with the age of 4300 year B.P., the calcite grain content is about 64%, and the quartz content is about 35%. Within the B horizons of soils on the dunes from 83 000 years B.P. to 347 000 years B.P., the calcite grain content is only 1–2%; however, the quartz grain content is about 92%. In the B2 horizons of soils on the dune of 690 000 years B.P. and on the Tertiary plateau, there are some calcite grains but the quartz grain content is about 96%. (3) The average size of quartz grains in the soils on the sand dunes from 4300 B.P. to 347 000 years B.P. is generally smaller, but the average size of quartz on the sand dunes of 690 000 year B.P. becomes larger and the grains are well rounded. On the Tertiary limestone plateau, the average quartz size becomes again smaller, and the grains are more rounded. (4) Fet in B2 horizon of the soil profiles increases clearly corresponding to the age. Iron activity expressed by Feo/Fed also shows a close relation to the chronological sequence. The B horizon of the soil profiles shows a drastic decrease of Feo/Fed according to the age. Iron crystalinity, (Fed-Feo)/Fet, has a tendency for a positive relation with increasing age. Received: 1 June 1995 · Accepted: 4 December 1995  相似文献   

2.
Soil chronofunctions are often quasilinear, but those relationships may be only gross, fortuitous generalizations that ignore changes in soils resulting from climatic and other cyclic external influences that govern soil formation or soil degradation. In the Rocky Mountains, soil development has been extensively used to estimate the age of sediments, but the number of soils is usually few, and large ranges in values for soil data may be dismissed as “normal variation.” In a detailed study of soils in the Wind River Range and Wind River Basin, characteristics of near-surface horizons do not follow age trends. However, the underlying carbonate-bearing horizons do have age-related characteristics. This “soil paradox” may be related to glacial–interglacial cycles in which (1) wind erodes near-surface horizons and then provides new parent material and (2) cryoturbation disrupts carbonate horizons, remobilizing carbonate and changing carbonate morphology but with only minimal loss of carbonate from the soil.  相似文献   

3.
In South China, the Datangpo black shales (663 Ma–654.5 Ma) were deposited during the Cryognian interglacial time between the Sturtian and Marinoan glaciations. Multi-geochemical proxies, including different iron speciation and relevant ratios (FeHR/FeT, FeP/FeHR and FeT/Al ratios) and molybdenum concentrations, were used to reconstruct the paleo-depositional environment of this black shale horizon. The ratios of different iron species (FeHR/FeT > 0.38 and FeP/FeHR < 0.80) suggest an overall anoxic conditions (ferruginous) over the deposition of the black shales, although intermittent euxinic (FeHR/FeT > 0.38 and FeP/FeHR ≈ 0.80) and oxic (FeHR/FeT < 0.38) intervals could have occurred. Furthermore, FeT/Al ratios (FeT/Al ≤ 0.51) confirm that water column may not be persistent euxinia during the deposition of the Datangpo black shales. Meanwhile, molybdenum concentrations show a decreasing trend towards the top of the black shales, reconciling the gradual oxygenating trend during this period as stated above. Compared to δ34SPy values in the Mesoproterozoic deep ocean, more positive δ34SPy values of this study may result from a small size of sulfate reservoir. The small-size sulfate reservoir and concurrent enrichment of molybdenum indicate that the ocean chemistry in the Cryogenian Period is similar to that in the Archean Eon.  相似文献   

4.
The abandoned Hg mine in Podljubelj was in operation with interceptions from 1557 to 1902. The entire operating period yielded about 110 000 tons of ore, from which 360 tons of Hg was produced. The objective of the research project was to establish the contents and spatial distribution of Hg in soils and stream sediments in the vicinity of the mine. On an area of 88 ha the soil was sampled in a 100 × 100 m grid. Two soil horizons (0–5 cm and 20–30 cm) were sampled in order to distinguish between geogenic and anthropogenic Hg sources. It was established that on an area of about 9 ha Hg content in soil exceeds The New Dutchlist action value for Hg (10 mg/kg). Total Hg concentrations in soil samples vary between 0.17 and 719 mg/kg, with a mean of 3.0 mg/kg. Mercury contents in stream sediments range from 0.065 to 1.4 mg/kg, with a mean of 0.64 mg/kg. The highest determined value in soils was found in the area around the former roasting furnace, where the ore was processed. Increased Hg concentrations were also found on the mine waste dump (108 mg/kg). Mercury contents in soils generally decrease with soil profile depth and with the distance from the mine and from the roasting furnace location. Mercury also appears in higher concentrations along the road that runs through the valley, which results from the use of Hg-bearing ore residues in road construction. The average enrichment factor (EF) of Hg in topsoil with respect to subsoil is 3.3. Calculated enrichment factors show higher values also for Cd (3.2), Pb (2.7), Ca (2.4) and P (1.9). The average enrichment factor of Hg in topsoil with regard to the established Slovenian soil averages (EFslo) is 19. EFslo of other determined chemical elements do not exceed 3.0.  相似文献   

5.
This paper presents the results of an integrated U-Pb detrital zircon geochronology and Si-in-white mica analysis for synorogenic sediments in the Jianghan Basin to the south of the Dabie Orogen. The results provide an improved understanding of the provenance of these sediments and the unroofing pattern of the early Mesozoic Dabie Mountain. Si contents of detrital white micas range from 3.09 to 3.34 atoms pfu for the upper Triassic sandstones whereas 3.06 to 3.59 atoms pfu for the lower and middle Jurassic sandstones. The majority of detrital white micas in the lower Jurassic sandstones is phengitic and originated exclusively from the Dabie high- to ultrahigh- pressure rocks. The U-Pb dating results of the detrital zircons for seven samples suggest that these synorogenic sediments have a significant change of provenance from late Triassic to early and middle Jurassic. For the upper Triassic sandstone, the U-Pb age clusters of these zircons are characterized by ~ 420-450 Ma, ~ 750-820 Ma, ~ 1050-1200 Ma and ~ 2500 Ma with minor Luliangian (~ 1700–2000 Ma) components. In contrast, the zircon ages of the Jurassic sandstones are dominated by the Luliangian (~ 1700–2000 Ma) ages with only minor Caledonian (~ 420-450 Ma) and Greenville (~ 1050-1200 Ma) ages. In combination with other available geological data, it can be concluded that the Dabie HP-UHP rocks might initially be exposed to the surface at the beginning of early Jurassic (~ 190 Ma). The Jiangnan terrain (also named “Jiangnan old continental in Chinese) to the south of the Jianghan basin provided the predominant supply of upper Triassic sediments, whereas the Paleoproterozoic Yangtze crustal materials (overlying the present Dabie Complex at the time) were the important provenance of the Jurassic sediments in the Jianghan basin.  相似文献   

6.
A red soil profile in Xuancheng, Anhui province, southern China, in the middle to lower reaches of the Yangtze River, was investigated using X‐ray diffraction, X‐ray fluorescence spectrometer, and scanning electron microscopy. The mobile components K2O and Na2O and trace elements Ba and Sr of the Xuancheng section exhibit a general trend of decrease downward along the red soil profile, together with an increase downward of chemical index of alteration (CIA) values, suggesting more intense depletion in the lower portion than in the upper portion. The major components SiO2, Al2O3 and Fe2O3, as well as SiO2/Al2O3, SiO2/Fe2O3 and Al2O3/Fe2O3 ratios, show notable fluctuations along the soil profile, indicating intense climatic oscillations in the area during the Pleistocene age. The clay mineral assemblage of the Xuancheng section can be generally subdivided into three groups, suggesting a general trend of three stages of climate changes. The lower portion of ~10.4–6.3 m depth has a lower illite content and higher abundance of kaolinite and illite–smectite (I/S) clays, indicating that a warm and wet climate prevailed over the episode of ca. 600–350 ka BP. A decrease in abundance of kaolinite and I/S clays and increase in illite content at a depth of ~6.3–2.2 m probably indicate a transition stage of climate change from warm/humid to cool/dry in the period ca. 350–80 ka BP. The higher illite content and lower abundance of kaolinite and I/S clays in the upper portion of ~2.2–0 m depth suggest that a relatively cool and dry climate dominated since ca. 80 ka BP. Based on changes in clay mineralogy and chemical indices of the sediments, seven warm/cold fluctuations were determined in the area since the Middle Pleistocene. Climate changes documented in the Xuancheng section are in agreement with the δ18O records of sediments from the equatorial Pacific Core V28‐238 and the loess–palaeosol sequences in the Loess Plateau of northwestern China. Correlated to the episode of S4 and S5 soil units in the Loess Plateau, the period of ca. 600–350 ka BP in the Xuancheng area was dominated by the particularly strong East Asia summer monsoon, as indicated by its most abundant kaolinite and I/S clays. Fluctuations in clay mineralogy along the Xuancheng soil profile were mainly controlled by both the East Asia summer and winter monsoons in response to the global changes in the Middle–Late Pleistocene. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

7.
Upper crustal abundances of trace elements: A revision and update   总被引:7,自引:0,他引:7  
Zhaochu Hu  Shan Gao   《Chemical Geology》2008,253(3-4):205-221
We report new estimates of abundances of rarely analyzed elements (As, B, Be, Bi, Cd, Ge, In, Mo, Sb, Sn, Te, Tl, W) in the upper continental crust based on precise ICP-MS analyses of well-characterized upper crustal samples (shales, pelites, loess, graywackes, granitoids and their composites) from Australia, China, Europe, New Zealand and North American. Obtaining a better understanding of the upper crustal abundance and associated uncertainties of these elements is important in placing better constraints on bulk crust composition and, from that, whole Earth models of element cycling and crust generation. We also present revised abundance estimates of some more commonly analyzed trace elements (Li, Cr, Ni, and Tm) that vary by > 20% compared to previous estimates. The new estimates are mainly based on significant (r2 > 0.6) inter-element correlations observed in clastic sediments and sedimentary rocks, which yield upper continental crust elemental ratios that are used in conjunction with well-determined abundances for certain key elements to place constraints on the concentrations of the rarely analyzed elements. Using the well-established upper crustal abundances of La (31 ppm), Th (10.5 ppm), Al2O3 (15.40%), K2O (2.80%) and Fe2O3 (5.92%), these ratios lead to revised upper crustal abundances of B = 47 ppm, Bi = 0.23 ppm, Cr = 73 ppm, Li = 41 ppm, Ni = 34 ppm, Sb = 0.075, Te = 0.027 ppm, Tl = 0.53 ppm and W = 1.4 ppm. No significant correlations exist between Mo and Cd and other elements in the clastic sediments and sedimentary rocks, probably due to their enrichment in organic carbon. We thus calculate abundances of these elements by assuming the upper continental crust consists of 65% granitoid rocks plus 35% clastic sedimentary rocks. The validity of this approach is supported by the similarity of SiO2, Al2O3, La and Th abundances calculated in this way with their upper crustal abundances given in Rudnick and Gao [Rudnick, R., Gao, S., 2003. Composition of the continental crust. In: Rudnick, R.L. (Ed.), The Crust. In: Holland, H.D., Turekian, K.K. (Eds.), Treatise on Geochemistry, vol. 3. Elsevier–Pergamon, Oxford, pp. 1–64.]. The upper crustal abundances thus obtained are Mo = 0.6 ppm and Cd = 0.06 ppm. Our data also suggest a  20% increase of the Tm, Yb and Lu abundances reported in Rudnick and Gao [Rudnick, R., Gao, S., 2003. Composition of the continental crust. In: Rudnick, R.L. (Ed.), The Crust. In: Holland, H.D., Turekian, K.K. (Eds.), Treatise on Geochemistry, vol. 3. Elsevier–Pergamon, Oxford, pp. 1–64.].  相似文献   

8.
Changes in the urban environment of Dhaka City have been evaluated from the geochemical compositions of bottom sediments from two lakes, Gulshan-1 and –2. Abundances of Pb, Zn, Fe2O3 and total sulfur in a Gulshan-1 core gradually increase toward the sediment–water interface. Three stages of condition change can be recognized in Gulshan-1, based on trace metal concentration patterns. The basal Stage I corresponds to background Dhaka sedimentation, whereas gradual increase in Stage II represents the beginning of pollution. Marked increases in Pb and Zn in Stage III reflect rapid urban development and increased emissions to the atmosphere. The condition of the Dhaka environment is compared to that of Japan based on Zn–Fe2O3 and Pb–Fe2O3 relations. Zn–Fe2O3 ratios in Stage I Dhaka sediments are similar to normal Japanese sediments, whereas Stage II data lie on the same trend as Japan urban sediments. Dhaka Stage III samples have greater Zn:Fe2O3 ratios than Japanese urban sediments, suggesting Zn pollution from poorly-controlled industrial sources. In contrast, the Dhaka Pb–Fe2O3 trend lies between normal and urban Japanese sediments. Although vehicle emissions in Dhaka are now significant, the data suggest that Pb pollution from this source remains in its early stages.  相似文献   

9.
Ten highly weathered soils in southeastern Nigeria were sampled from their typical A and B horizons for analyses. The objectives were to determine the different forms of Fe and Al oxides in the soils and relating their occurrence to phosphate availability and retention in the soils. The soils are deep and often physically degraded but are well drained and coarse in the particle size distribution. They are mostly dominated by kaolinite in their mineralogy with very high values of SiO2. The soils are acidic with low soil organic carbon (SOC) contents. The elements in the exchange complex are also low thus reflecting in the low CEC of the soil. Available phosphorus (P) in the soils are generally low while total P ranged from 157 to 982 mg kg−1 with an overall average of 422 mg kg−1. Total Fe in the soil is highest and their order represented as follows: Fet > Fed > Feox ≥ Fep. The pyrophosphate extractable Fe was always higher in the top soil than in the subsoil and was attributed to the fact that these forms of Fe are associated with organic matter which is more abundant in topsoil than in subsoil. Like in Fe forms, the order of Al occurrence could generally be presented as; Alt > Ald > Alox > Alp. More Fe and Al oxides in the soils are strongly crystalline while a small quantity is poorly crystalline Fe forms. The amorphous forms of both Fe and Al are very low in the soils when compared with the crystalline forms. The oxides that show very strong affinity to total P are Fed–Feox, Fed, Ald, Fet, Feox and Alox/Ald. To overcome this problem of P retention in the soil, we recommend constant liming of these soils to neutralize them, application of organic matter and of high dosage of phosphate fertilizer to the soils.  相似文献   

10.
The role of the uppermost mantle strength in the pattern of lithosphere rifting is investigated using a thermo-mechanical finite-element code. In the lithosphere, the mantle/crust strength ratio (SM/SC) that decreases with increasing Moho temperature TM allows two strength regimes to be defined: mantle dominated (SM > SC) and crust dominated (SM < SC). The transition between the two regimes corresponds to the disappearance of a high strength uppermost mantle for TM > 700 °C. 2D numerical simulations for different values of SM/SC show how the uppermost mantle strength controls the style of continental rifting. A high strength mantle leads to strain localisation at lithosphere scale, with two main patterns of narrow rifting: “coupled crust–mantle” at the lowest TM values and “deep crustal décollement” for increasing TM values, typical of some continental rifts and non-volcanic passive margins. The absence of a high strength mantle leads to distributed deformations and wide rifting in the upper crust. These numerical results are compared and discussed in relation with series of classical rift examples.  相似文献   

11.
The prevailing theory for the formation of trona [Na3(CO3)(HCO3) · 2(H2O)] relies on evaporative concentration of water produced by silicate hydrolysis of volcanic rock or volcaniclastic sediments. Given the abundance of closed drainage basins dominated by volcanics, it is puzzling that there are so few trona deposits and present-day lakes that would yield dominantly Na–CO3 minerals upon evaporation. Groundwater in the San Bernardino Basin (southeastern Arizona, USA and northeastern Sonora, Mexico) would yield mainly Na–CO3 minerals upon evaporation, but waters in the surrounding basins would not. Analysis of the chemical evolution of this groundwater shows that the critical difference from the surrounding basins is not lithology, but the injection of magmatic CO2. Many major deposits of trona and Na–CO3-type lakes appear to have had “excess” CO2 input, either from magmatic sources or from the decay of organic matter. It is proposed that, along with the presence of volcanics, addition of “excess” CO2 is an important pre-condition for the formation of trona deposits.  相似文献   

12.
Reactions of CO2 with carbonate and silicate minerals in continental sediments and upper part of the crystalline crust produce HCO3 in river and ground waters. H2SO4 formed by the oxidation of pyrite and reacting with carbonates may produce CO2 or HCO3. The ratio, ψ, of atmospheric or soil CO2 consumed in weathering to HCO3 produced depends on the mix of CO2 and H2SO4, and the proportions of the carbonates and silicates in the source rock. An average sediment has a CO2 uptake potential of ψ = 0.61. The potential increases by inclusion of the crystalline crust in the weathering source rock. A mineral dissolution model for an average river gives ψ = 0.68 to 0.72 that is within the range of ψ = 0.63 to 0.75, reported by other investigators using other methods. These results translate into the CO2 weathering flux of 20 to 24 × 1012mol/yr.  相似文献   

13.
A 3-D density model for the Cretan and Libyan Seas and Crete was developed by gravity modelling constrained by five 2-D seismic lines. Velocity values of these cross-sections were used to obtain the initial densities using the Nafe–Drake and Birch empirical functions for the sediments, the crust and the upper mantle. The crust outside the Cretan Arc is 18 to 24 km thick, including 10 to 14 km thick sediments. The crust below central Crete at its thickest section, has values between 32 and 34 km, consisting of continental crust of the Aegean microplate, which is thickened by the subducted oceanic plate below the Cretan Arc. The oceanic lithosphere is decoupled from the continental along a NW–SE striking front between eastern Crete and the Island of Kythera south of Peloponnese. It plunges steeply below the southern Aegean Sea and is probably associated with the present volcanic activity of the southern Aegean Sea in agreement with published seismological observations of intermediate seismicity. Low density and velocity upper mantle below the Cretan Sea with ρ  3.25 × 103 kg/m3 and Vp velocity of compressional waves around 7.7 km/s, which are also in agreement with observed high heat flow density values, point out at the mobilization of the upper mantle material here. Outside the Hellenic Arc the upper mantle density and velocity are ρ ≥ 3.32 × 103 kg/m3 and Vp = 8.0 km/s, respectively. The crust below the Cretan Sea is thin continental of 15 to 20 km thickness, including 3 to 4 km of sediments. Thick accumulations of sediments, located to the SSW and SSE of Crete, are separated by a block of continental crust extended for more than 100 km south of Central Crete. These deep sedimentary basins are located on the oceanic crust backstopped by the continental crust of the Aegean microplate. The stretched continental margin of Africa, north of Cyrenaica, and the abruptly terminated continental Aegean microplate south of Crete are separated by oceanic lithosphere of only 60 to 80 km width at their closest proximity. To the east and west, the areas are floored by oceanic lithosphere, which rapidly widens towards the Herodotus Abyssal plain and the deep Ionian Basin of the central Mediterranean Sea. Crustal shortening between the continental margins of the Aegean microplate and Cyrenaica of North Africa influence the deformation of the sediments of the Mediterranean Ridge that has been divided in an internal and external zone. The continental margin of Cyrenaica extends for more than 80 km to the north of the African coast in form of a huge ramp, while that of the Aegean microplate is abruptly truncated by very steep fractures towards the Mediterranean Ridge. Changes in the deformation style of the sediments express differences of the tectonic processes that control them. That is, subduction to the northeast and crustal subsidence to the south of Crete. Strike-slip movement between Crete and Libya is required by seismological observations.  相似文献   

14.
The oolitic iron ore of the Gara Djebilet field occurs within the Early Devonian sediments of the Tindouf Basin (Algerian Sahara), particularly in the Upper Djebilet Formation of Pragian age. Three large lenses form three individual deposits, extending E-W for about 60 km, namely Gara West, Gara Center and Gara East.The mineralization is interbedded with argillaceous to sandy sediments and it can be related to a barrier island palaeoenvironment, bordered by an inner lagoon or shallow embayment and an epicontinental sea. Trapped by Palaeozoic shoals, the oolitic sediments show a mineralogy marked mainly by magnetite, hematite, goethite, maghemite, chamosite (bavalite), siderite, apatite and quartz. Three paragenetic associations present a vertical distribution with a Lower non-magnetitic ore, a magnetitic ore and an Upper non-magnetitic ore.Three petrographical facies types have been defined: a cemented facies (FOC); a detrital facies (FOD); and a non-detrital facies (FOND).Chemical data for the whole field show a difference between the Lower non-magnetitic ore (Fe=54.6%), the Magnetitic ore (Fe=57.8%) and the Upper non-magnetitic ore (Fe=53%). The Magnetitic ore, which corresponds mainly to the workable ore (cutoff grade at 57%), has the following composition: SiO2=4.9%, Al2O3=4.2%, Fe2O3=61.43%, FeO=19.2%, and P2O5=1.8%. The corresponding calculated economical ore reserves are 985×106t, with 57.8% Fe.Regarding the genesis of the oolitic iron ore, a southern source is suggested for the iron, with deposition taking place in a quiet environment. There, the ooids developed by an intrasedimentary accretion mechanism around detrital grain within an iron-rich mud.The Gara Djebilet field is an important occurrence of the “North African Palaeozoic Ironstone Belt” extending from the Zemmour to Libya which also includes ironstones of Ordovician, Silurian and Devonian age.  相似文献   

15.
Oxygenation of the Earth's atmosphere occurred in two major steps, near the beginning and near the end of the Proterozoic Eon (2500 to 542 Ma ago), but the details of this history are unclear. Chromium isotopes in iron-rich chemical sediments offer a potential to highlight fine-scale fluctuations in the oxygenation of the oceans and atmosphere and to add a further dimension in the use of redox-sensitive tracers to solve the question regarding fluctuations of atmospheric oxygen levels and their consequences for Earth's climate. We observe strong positive fractionations in Cr isotopes (δ53Cr up to + 5.0‰) in iron-rich cherts and banded iron formation horizons within the Arroyo del Soldado Group (Ediacaran; Uruguay) that can be explained by rapid, effective oxidation of Fe(II)-rich surface waters. These fluctuations are correlated with variations in ratios of highly reactive iron (FeHR) to total iron (Fetot) which indicate a predominance of anoxic water columns (FeHR/Fetot > 0.38) during the onset of oxidation pulses. We favor the scenario by which isotopically heavy Cr(VI) entered the basin after pulses of oxidative weathering on land and in which Fe(II) accumulated in the water column. Neodymium isotopes reveal that these oxygenation pulses were followed by increased influxes to the basin of continental crust-derived detrital components of Paleoproterozoic (Nd TDM model ages = 2.1–2.2 Ga) provenance typical of the Rio de la Plata Craton. The association of positive δ53Cr–ferruginous (FeHR/Fetot > 0.38) stratigraphic intervals with low-diversity acritarch assemblages dominated by Bavlinella faveolata strongly support models postulating a stratified, eutrophic Neoproterozoic ocean. Thus, even within a few million years of the Precambrian–Cambrian boundary, paleoceanographic conditions resembled more those of Paleoproterozoic oceans than Phanerozoic and present oceans. This highlights the sheer magnitude of ecological changes at the Precambrian–Cambrian transition, changes which ultimately led to the demise of the Precambrian world and the birth of the metazoan-dominated Phanerozoic.  相似文献   

16.
The Vazante Group consists of Precambrian carbonate-dominated platform deposits that extend along more than 300 km in the external zone of the Brasilia Fold Belt of the São Francisco Basin in east central Brazil. The sequence is about 4.8 km thick and contains a preserved glaciomarine diamictite unit (containing dropstone) at the top and a lower diamictite unit at the bottom. Previous C- and Sr-isotope profiles suggested the correlation of the upper diamictite unit with the “Sturtian” glacial event (ca. 750–643 Ma). However, new Re–Os isotope data from the shales associated with the upper diamictites yield radiometric age estimates between 993 ± 46 and 1100 ± 77 Ma. U–Pb measurements on a suite of clear euhedral zircon crystals that were separated from the same shales associated with the upper diamictite and from the arkosic sandstone above the lower diamictite yield ages as young as 988 ± 15 and 1000 ± 25 Ma, respectively. Based on the Re–Os and U–Pb ages, the best age estimate of the Vazante Group is constrained to be 1000–1100 Ma and thus the two diamictite units are not correlative with the Sturtian glaciation(s) but most likely are records of glacial events that occurred during the late Mesoproterozoic.  相似文献   

17.
Series of α, β, ω and (ω-1) hydroxy fatty acids (FAOHs) were determined in several freshwater and brackish water lacustrine sediments in Japan. Analytical procedure used was digestion of the solvent-extracted sediment with HF/HCl followed by solvent and saponification extraction of the residue. Abundances of α/β and ω-FAOH determined by this procedure were 2–3 times higher than those obtained by single alkaline saponification and of the same order with those provided by HCl hydrolysis. Major portion of α/β-FAOH was obtained by solvent extraction of the acid-treated sediments, while subsequent alkaline saponification was needed for the majority of ω-FAOH to be recovered. Thus determined FAOHs comprised 33–61% (Av. = 42%) of the “bound” acid constituents in the lacustrine surface sediments. The α/β and ω-FAOH composition was principally the same among the samples examined, except for relative proportions of the iso to anteiso C15 and C17 ß(α)-FAOH, which showed significant variations in the ranges of 0.30–1.1 and 0.46–1.5, respectively. In the holomictic lakes, the ratios together with the same ratios of the “bound” branched monocarboxylic acids tended to decrease with increasing water depth of the lakes, suggesting that the ratios may indicate an extent of the early diagenetic alteration of the bacteria-derived lipids either in water column or in surface sediment.  相似文献   

18.
Analysis of fault system in the high-P/T type Sambagawa metamorphic rocks of central Shikoku, southwest Japan, shows that conjugate normal faults pervasively developed in the highest-grade biotite zone (upper structural level) in three study areas (Asemi river, Oriu and Niihama areas). These conjugate normal faults consist of NE–SW to E–W striking and moderately north-dipping (set A), and NNW–SSE striking and moderately east dipping (set B) faults. The fault set A is dominant compared to the fault set B, and hence most of deformation is accommodated by the fault set A, leading to non-coaxial deformation. The sense of shear is inferred to be a top-to-the-WNW to NNW, based on the orientations of striation or quartz slickenfibre and dominant north-side down normal displacement. These transport direction by normal faulting is significantly different from that at D1 penetrative ductile flow (i.e. top-to-the-W to WNW). It has also been found that these conjugate normal faults are openly folded during the D3 phase about the axes trending NW–SE to E–W and plunging west at low-angles or horizontally, indicating that normal faulting occurred at the D2 phase. D2 normal faults, along which actinolite breccia derived from serpentinite by metasomatism sometimes occurs, perhaps formed under subgreenschist conditions (ca. 250 °C) in relation to the final exhumation of Sambagawa metamorphic rocks into the upper crustal level. The pervasive development of D2 normal faults in the upper structural level suggests that the final exhumation of Sambagawa metamorphic rocks could be caused by “distributed extension and normal faulting (removal of overburden)” in the upper crust.  相似文献   

19.
Formation of volcanogenic massive sulfide deposits: The Kuroko perspective   总被引:3,自引:0,他引:3  
The main objective of this paper is to identify the geochemical, hydrological, igneous and tectonic processes that led to the variations in the physical (size, geometry) and chemical (mineralogy, metal ratios and zoning) characteristics of volcanogenic massive sulfide deposits with respect to space (from a scale of mining district size area to a global scale) and time (from a < 10 000 year time scale to a geologic time scale).All volcanogenic massive sulfide deposits (VMSDs) appear to have formed in extensional tectonic settings, such as at mid ocean spreading centers, backarc spreading centers, and intracontinental rifts (and failed rifts). All VMSDs appear to have formed in submarine depressions by seawater that became ore-forming fluids through interactions with the heated upper crustal rocks. Submarine depressions, especially those created by submarine caldera formation and/or by large-scale tectonic activities (e.g., rifting), become most favorable sites for the formation of large VMSDs because of hydrological, physical and chemical reasons.The fundamental processes leading to the formation of VMSDs include the following six processes:
1. (1) Intrusion of a heat source (typically a 103 km size pluton) into an oceanic crust or a submarine continental crust causes deep convective circulation of seawater around the pluton. The radius of a circulation cell is typically 5 km. The temperature of fluids that discharge on the seafloor increases with time from the ambient temperature to a typical maximum of 350°C, and then decreases gradually to the ambient temperatures in a time scale of 100 to 10 000 years. The majority of sulfide and sulfate mineralization occurs during the waxing stage of hydrothermal activity.
2. (2) Reactions between low temperature (T < 150°C) country rocks with downward percolating seawater cause to precipitate seawater SO2−4 as disseminated gypsum and anhydrite in the country rocks.
3. (3) Reactions of the “modified” seawater with higher-temperature rocks at depths during the waxing stage cause the transformation of the “seawater” to metal- and H2S-rich ore-forming fluids. The metals and sulfide sulfur are leached from the county rocks; the previously formed gypsum and anhydrite are reduced by Fe2+-bearing minerals and organic matter, providing additional H2S. The mass of high temperature rocks that provide the metals and reduced sulfur is typically 1011 tons ( 40 km3 in volume). The roles of magmatic fluids or gases are minor in most massive sulfide systems, except for SO2 to produce acid-type alteration in some systems.
4. (4) Reactions between the ore-forming fluids and cooler rocks in the discharge zone cause alteration of rocks and precipitation of some ore minerals in the stockwork ores.
5. (5) Mixing of the ore-forming fluids with local seawater within unconsolidated sediments and/or on the seafloor causes precipitation of “primitive ores” with the black ore mineralogy (sphalerite + galena + pyrite + barite + anhydrite).
6. (6) Reactions between the “primitive ores” with later and hotter hydrothermal fluids cause transformation of “primitive ores” to “matured ores” that are enriched in chalcopyrite and pyrite.
Variations in the mineralogical and elemental characteristics, the geometry, and the size of submarine hydrothermal deposits are controlled by the following four parameters:
1. (A) The chemical and physical characteristics of seawater (composition, temperature, density), which depend largely on the geographical settings (e.g., equatorial evaporating basins),
2. (B) The chemical and physical characteristics of the plumbing system (lithology, fractures),
3. (C) The thermal structure of the plumbing system, which is determined largely by the ambient geothermal gradient, and the size and temperature of the intrusive, and
4. (D) The physical characteristics of the seafloor (depth, basin topography).
For example, the submarine hydrothermal deposits developed in basaltic plumbing systems are generally poor in Pb and Ba compared to those developed in felsic plumbing systems. The lower temperature systems are generally poorer in sulfides, but richer in iron oxides and sulfates. The higher temperature and larger hydrothermal systems tend to produce chalcopyrite and pyrite rich ores. Contrasts in the metal ratios between the Noranda-type Archean VMSDs and the younger VMSDs reflect the differences in the geothermal gradient of the plumbing systems. The submarine hydrothermal deposits developed in the near equatorial regions tend to form large continuous bedded type ores because of the likeliness of creating large stratified basins.The basic processes of submarine hydrothermal mineralization have remained essentially the same throughout the geologic history, from at least 3.5 billion year ago to the present.  相似文献   

20.
In this paper we present a detailed record of proxy-climatic events in the coastal belt of the eastern Mediterranean during the past 53,000 years. A sequence of alternating palaeosols, aeolianites, and dune sands, which have been dated by luminescence and by 14C, was studied by the magnetic susceptibility, particle-size distribution, clay mineralogy and soil micromorphology. Thirteen proxy-climatic events, demonstrating fluctuations of relatively dry and wet episodes, were recognized. The soil parent materials, as well as the different soil types, were rated in a semi-quantitative “dry” to “wet” scale. The palaeosol sequence is compared to a proxy-climatic record of oxygen and carbon isotopes in speleothems from a karstic cave in central Israel and to a record of lake levels of Lake Lisan and its successor, which is known as the Dead Sea. A genuine red Mediterranean Soil (Rhodoxeralfs), localy designated as “Hamra Soil” developed during the Last Glacial Stage, from 40 to 12.5 thousand calendar years BP. Climatic fluctuations that were recorded in speleothems and in changing lake levels were not preserved in this soil. During the cold and dry Younger Dryas, ca 12.5 to 11.5 calendar ka BP, a thick bed of loess material, deriving from atmospheric dust of the Sahara and Arabian deserts, covered the entire coastal belt. During this phase Lake Lisan was desiccated and turned into the modern, smaller Dead Sea. During the early Holocene, some 10–7.5 calendar ka BP, a second Red Hamra soil developed in warm and wet environments, associated with a relatively high stand of the Dead Sea level. A depletion of δ18O and a significant enrichment of δ13C in the speleothems were recorded during this episode. This event was in phase with the widespread distribution of freshwater lakes in the Sahara Desert and the accumulation of the S1 Sapropel in the eastern Mediterranean. Several small-scale dry and somewhat wet fluctuations of the Late Holocene, from 7.5 calendar ka BP to the present, were recorded in the coastal belt. Changes in human history, as reflected in archaeological records, are associated with proxy-climatic fluctuations. Periods of desertification and deterioration are coupled with dry episodes; periods of relative human prosperity are coupled with wetter episodes.  相似文献   

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