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1.
Coexisting fine-grained (0.1–20 μm) authigenic silicate minerals separated from altered tuffs in Miocene and Plio-Pleistocene lacustrine deposits were characterized petrographically and using X-ray powder diffraction. The authigenic minerals are dominated by clinoptilolite, erionite, phillipsite, K-feldspar, silica, calcite, smectite, and randomly interstratified illite/smectite. Minor accessories of opal-CT, cristobalite, and barite are present with the major alteration minerals. Authigenic minerals from altered tuffs were dated using the K/Ar method to evaluate the utility of these minerals for determining the time of alteration in low-temperature diagenetic environments. The eruption ages of some of these zeolite-rich tuffs were determined using the 40Ar/39Ar method on single sanidine and plagioclase minerals. The K/Ar isotopic ages of the fine-grained K-feldspar show minimal variation compared with results from the clinoptilolite separates. The isotopic ages from the authigenic K-feldspar (15-13.8 Ma) and some of the zeolites (16.-6.7 Ma) are similar to the eruption ages of the tuffs and indicate early alteration. Despite their open-framework structure, zeolites apparently can retain part or all of their radiogenic argon under favorable conditions (e.g., saturated environment). How much of the radiogenic argon is retained is estimated from the isotopic ages of other coexisting secondary minerals that are commonly dated by the K/Ar method. Although zeolite isotopic ages should be interpreted with caution, they may be useful to constrain temporal relations of low-temperature diagenetic processes when used in conjunction with other dateable minerals.  相似文献   

2.
The results of 10Be and 9Be measurements in several sections of ten large manganese nodules are presented along with U and Th isotope data on five of them.The 10Be and 10Be/9Be methods yield growth rates (covering a period of 5–10 Ma) which are in excellent agreement with each other. In three cases, these rates are also in very good agreement with those derived from the 230Th methods, whereas in the other two the 230Th-based rates are faster by over a factor of two.Based on the discrepancy between the inventory of 10Be (as well as 230Th) in nodules and the overhead seawater column, it is calculated that the former scavenge their Be and Th isotopes from 2–900 m of the overhead water column. The deduced 9Be concentrations of ocean water based on its 10Be contents and the 10Be/9Be ratios of nodule surfaces are found to be in good agreement with the direct 9Be measurements of seawater implying that 9Be in nodules (like10Be) is mostly authigenic.  相似文献   

3.
A sequential chemical extraction procedure was developed and tested to investigate the utility of meteoric 10Be as a tracer for authigenic mineral formation beneath the East Antarctic Ice Sheet. Subglacial meltwater is widely available under the Antarctic Ice Sheet and dissolved gases within it have the potential to drive chemical weathering processes in the subglacial environment. Meteoric 10Be is a cosmogenic nuclide with a half-life of 1.39·106 years that is incorporated into glacier ice, therefore its abundance in the subglacial environment in Antarctica is meltwater dependent. It is known to adsorb to fine-grained particles in aqueous solution, precipitate with amorphous oxides/hydroxides, and/or be incorporated into authigenic clay minerals during chemical weathering. The presence of 10Be in chemical weathering products derived from beneath the ice therefore indicates chemical weathering processes in the subglacial environment. Freshly emerging subglacial sediments from the Mt. Achernar blue ice moraine were subject to chemical extractions where these weathering phases were isolated and 10Be concentrations therein quantified. Optimization of the phase isolation was developed by examining the effects of each extraction on the sample mineralogy and chemical composition. Experiments on 10Be desorption revealed that pH 3.2–3.5 was optimal for the extraction of adsorbed 10Be. Vigorous disaggregation of the samples before grain size separations and acid extractions is crucial due to the incorporation of the nuclide in clay minerals and its preferential absorption to clay-sized particles. 10Be concentrations of 2–22·107 atoms·g−1 measured in oxides and clay minerals in freshly emerging sediments strongly indicate subglacial chemical weathering in the catchment of the Mt. Achernar moraine. Based on total 10Be sample concentrations, local basal melt rates, and 10Be ice concentrations, sediment-meltwater contact in the subglacial environment is on the order of thousands of years per gram of underlying fine sediment. Strong correlation (R = 0.97) between 10Be and smectite abundance in the sediments supports authigenic clay formation in the subglacial environment. This suggests meteoric 10Be is a useful tool to characterize subglacial geochemical weathering processes under the Antarctic Ice Sheet.  相似文献   

4.
A block of sulfide crust collected from an active hydrothermal mound in an Archaean site (12°56.4′N, 143°37.9′E; depth ca. 3000 m) of the South Mariana Trough was dated using both 230Th/234U disequilibrium and electron spin resonance (ESR) methods to establish the growth duration. Eight subsamples from the sulfide crust were separated further into magnetic and non-magnetic fractions using a Franz isodynamic separator. Thirteen sulfide samples, soluble in nitric acid, yielded 230Th/234U ages of 0.3–2.2 ka. The magnetic fractions had significantly lower Th/U ratios, which enabled age determinations as precise as ±2% (2σ). The age distribution obtained for the section of sulfide crust analyzed is consistent with deposition of sulfide minerals from the upper surface of the crust to the inner side. The 230Th/234U ages of the sulfide minerals were compared with ESR ages of barites separated from 12 subsamples of the same sulfide crust. ESR ages of 0.27–1.3 ka show a spatial pattern broadly resembling that observed in 230Th/234U dating method. While there are some significant offsets, these results illustrate the potential of the two methods for use in investigation of the evolutional history of a hydrothermal system.  相似文献   

5.
230Th-238U radioactive disequilibrium was studied in the historical lava flows of the Mauna Loa and Kilauea, Hawaii. Large variations of the (230Th/232Th) ratio among lavas of the same volcano that were erupted at a few years' interval are interpreted as due to contamination. The contamination probably occurs by assimilation of zeolitic minerals formed by seawater interaction while the magma resides in a superficial chamber.  相似文献   

6.
Previous studies have shown how biogenic silica particles undergo conversion to aluminosilicate phases in large tropical deltaic systems, thus affecting the world ocean budget of major seawater cations. This study tackles the important question of the silica budget in the coastal zone of the Mississippi River Delta, providing evidence for the role of biogenic silica diagenesis in this subtropical system from direct examination of individual diatom particles, sediment leachates and pore-water composition. The estimated reactive silica stored in the study area (5990 km2) is based on operational leaches that account for altered biogenic silica particles and other authigenic aluminosilicate phases in addition to fresh biogenic silica. Early diagenesis of silica in the delta front occurs mainly where more siliceous material is deposited. An inner-shelf area, where hypoxic conditions are found, significantly contributes to the formation of authigenic products of Si alteration. Data suggest that the limiting factor of silica alteration processes is the availability of detrital phases such as Al and Fe. The estimated total reactive silica accumulation in the study area is 1.45×1010 mol Si year−1, representing ∼2.2% of the long-term bulk sediment accumulation. On the basis of a conservative appraisal, the authigenic mineral components account for ∼40% of the long-term reactive silica storage. This study shows that non-tropical deltaic systems are significantly more important sinks of silica than previously thought and that, where conditions are favourable, a consistent portion of reactive silica not leaving the shelf is stored within the delta in the form of authigenic components.  相似文献   

7.
The accumulation of extraterrestrial 3He, a tracer for interplanetary dust particles (IDPs), in sediments from the Ontong Java Plateau (OJP; western equatorial Pacific Ocean) has been shown previously to exhibit a regular cyclicity during the late Pleistocene, with a period of ∼100 ka. Those results have been interpreted to reflect periodic variability in the global accretion of IDPs that, in turn, has been linked to changes in the inclination of Earth’s orbit with respect to the invariable plane of the solar system. Here we show that the accumulation in OJP sediments of authigenic 230Th, produced by radioactive decay of 234U in seawater, exhibits a 100-ka cyclicity similar in phase and amplitude to that evident in the 3He record. We interpret the similar patterns of 230Th and 3He accumulation to reflect a common origin within the ocean-climate system. Comparing spatial and temporal patterns of sediment accumulation against regional patterns of biological productivity and against the well-established pattern of CaCO3 dissolution in the deep Pacific Ocean leads to the further conclusion that a common 100-ka cycle in accumulation of biogenic, authigenic and extraterrestrial constituents in OJP sediments reflects the influence of climate-related changes in sediment focusing, rather than changes in the rate of production or supply of sedimentary constituents.  相似文献   

8.
Ocean Drilling Program Site 658 lies under the North African summer dust plume, and ought to be an ideal target for optically stimulated luminescence (OSL) dating, since the main clastic input is far-travelled Saharan dust. However, OSL ages for coarse silt-sized quartz (40–63 μm) are systematically lower than independent age estimates when dose rates are calculated using a model which assumes detrital 238U, 232Th and 40K and excess 230Th and 231Pa. Ages which are in good agreement with independent age control are obtained from the coarse silt samples when a correction for authigenic uranium uptake is incorporated into the dose rate model. Authigenic uranium uptake occurs under reducing conditions, which are common at the sediment–water interface, and some degree of authigenic uranium correction may be required for most marine sediments. Using this revised dose rate model, ages produced using fine silt-sized quartz (4–11 μm) are up to 100% older than both independent and coarse silt ages. In addition, the fine silt ages show a consistent pattern of age decrease with depth over 1.5 m of core. 230Th data from Site 658 indicate that this site receives 3 times more sediment laterally than vertically. It is concluded that the fine silt at Site 658 contains a substantial reworked component, making it unsuitable for dating. Conversely the coarse silt fraction, which settles through water at ∼40 times the rate of fine silt, appears to be derived from dust input over the site at the time of deposition. Since prominent nepheloid (cloudy) layers occur in various deep ocean basins, and the material suspended in these layers often consists of reworked fine silt-sized sediments, coarser material should be dated where possible.  相似文献   

9.
Authigenic carbonates were sampled in methane-enriched piston core sediments collected from gas venting sites on the western continental slope of the Ulleung Basin, East Sea of Korea. Multidisciplinary investigations on these carbonates, including the scanning electronic microscope (SEM) observations and mineralogical-geochemical compositions, were carried out to identify the carbon and oxygen sources and the forming mechanism of these carbonates. The authigenic carbonates from the study area correspond to semi-consolidated, compact concretions or nodules ranging from 2 to 9 cm in size. X-ray diffraction and electron microprobe analyses showed that most of the sampled carbonate concretions were composed of almost purely authigenic high-Mg calcite (10.7–14.3 mol% MgCO3). Characteristically, microbial structures such as filaments and rods, which were probably associated with the authigenic minerals, were abundantly observed within the carbonate matrix. The carbonates were strongly depleted in δ13C (−33.85‰ to −39.53‰ Peedee Belemnite (PDB)) and were enriched in δ18O (5.16–5.60‰ PDB), indicating that the primary source of carbon is mainly derived from the anaerobic oxidation of methane. Such methane probably originated from the destabilization of the underlying gas hydrates as strongly supporting from the enriched 18O levels. Furthermore, the strongly depleted δ13C values (−60.7‰ to −61.6‰ PDB) of the sediment void gases demonstrate that the majority of the gas venting at the Ulleung Basin is microbial methane by CO2 reduction. This study provides another example for the formation mechanism of methane-derived authigenic carbonates associated with gas-hydrate decomposition in gas-seeping pockmark environments.  相似文献   

10.
Comparative UPb dating of zircon, xenotime and monazite from two different samples of the Himalayan “Makalu” granite shows the two U decay series to be in disequilibrium, particularly in monazite. This disequilibrium is due to excess or deficit amounts of radiogenic206Pb which originate from an excess or deficit of230Th, respectively, occurring initially in the mineral. Such an initial disequilibrium is caused by UTh fractionation between the crystallising mineral and the magma. Therefore, the UPb ages of Th-rich minerals such as monazite (and allanite) have to be corrected for excess206Pb due to excess230Th, whereas Th-poor minerals such as zircon and xenotime require a correction for a deficit of206Pb due to deficiency of230Th. The extent of this correction depends on the degree of ThU fractionation and on the age of the rock. For the two monazite populations analysed here, these excess amounts of206Pb were, with reference to the amount of radiogenic206Pb, 8–10% and 15–20% respectively, and less than 1% for zircon and xenotime. The varying degrees of Th enrichment relative to U in monazite show that the ThU partition coefficients for this mineral are not constant within a single granite. Furthermore, for monazite there is evidence for excess amounts of radiogenic207Pb originating from the decay of initial excess231Pa, also enriched during crystal growth.The very low Th/U ratios of 0.196 and 0.167, determined for thetwo whole rocks from which the minerals have been extracted, substantiate the view that granite formation is a fundamental mechanism for ThU fractionation in continental crust.The different ages of 21.9 ± 0.2m.y. and24.0 ± 0.4m.y., obtained by averaging the corrected238U206Pb ages of the monazites, suggest that the apparently homogeneous Makalu granite was generated over a period of at least 2 m.y.  相似文献   

11.
Noble and active gases are released from geological samples during gas extraction for noble gas isotope analyses. The active gases should be removed before inletting to mass spectrometers for the analyses. The normal noble gas preparation systems can clean up most geological samples. However, authigenic minerals from sedimentary rocks in oil/gas fields contain organic matter, which cannot be cleaned up by the normal preparation systems and thus influence the noble gas analyses. We introduce a novel gas purification system(PRC patent No. ZL201320117751.2), which includes several reversible purification pumps with different absorbing and degassing temperatures. It can well clean up water steam, carbon dioxide and organic gases. Mica minerals are often used for ~40Ar/~39 Ar dating. A muscovite sample(2082MS) which could not be cleaned up by the normal preparation system with two SAES NP10~#174; getters, becomes the test sample for a comparative experiment in this study. The experiment is assigned into 4 sections with the organic gas removal system(OGRS) "Closed/Opened" in turn. When the OGRS is closed only with two NP10 getters for purification, the ~40Ar intensities increase in curves with inlet time because of impurities, the ~40Ar/~39 Ar dating results yield age errors about ±2%–±1%(2σ). When the OGRS is opened for purification, in contrast, the ~40 Ar intensities decrease linearly with inlet time. This indicates that the gases have been cleaned up effectively, and the 4~0Ar/~39 Ar results yield ages with errors in ±0.4%. The OGRS is very helpful to obtain high-quality analysis data.  相似文献   

12.
The (U-Th)/He dating method applied to U-rich phases such as zircon and apatite has sufficient sensitivity and precision to be of potential use for dating relatively recent geologic events such as volcanic eruptions. However, in phases with crystallization ages less than ∼1 Ma, chemical fractionation within the 238U decay series may modify the He ingrowth rate, causing He ages computed from the secular equilibrium age equation to be incorrect. The resulting systematic error depends on the [230Th/238U] activity ratio of the dated phase when it is erupted, and on the eruption age. Zircons, which exclude Th relative to U, will likely have secular equilibrium He ‘ages’ that underestimate the eruption age by up to a few tens of %, decreasing with increasing eruption age. Apatites tend to accommodate U and Th with little fractionation, so apatite secular equilibrium He ages will be nearly concordant with eruption age. If minerals are erupted immediately after crystallization, the disequilibrium effect can be reasonably accounted for based on Th/U systematics. However, crystals are likely to reside for unknown but potentially long periods in a magma chamber, such that the degree of secular disequilibrium will be reduced prior to the onset of He accumulation. (U-Th)/He analyses of co-genetic phases that fractionate the U/Th ratio differently, like apatite and zircon, can be used to better constrain eruption age, as well as to provide insights into magma chamber residence time. We illustrate this approach with (U-Th)/He analyses of zircons and apatites of the Pleistocene-age Rangitawa Tephra, New Zealand.  相似文献   

13.
Using classical diffusion theory, we present a mathematical technique for the determination of 4He concentration profiles in minerals. This approach should prove useful for constraining the low-temperature cooling histories of individual samples and for correcting (U–Th)/He ages for partial diffusive loss. The calculation assumes that the mineral of interest contains an artificially produced and uniform distribution of 3He obtained by proton irradiation [Shuster et al., Earth Planet. Sci. Lett. 217 (2004) 19–32]. In minerals devoid of natural helium, this isotope allows measurement of He diffusion coefficients; in minerals with measurable radiogenic He, it permits determination of 4He profiles arising during ingrowth and diffusion in nature. The 4He profile can be extracted from stepwise degassing experiments in which the 4He/3He ratio is measured. The evolution of the 4He/3He ratio as a function of cumulative 3He released can be compared with forward models to constrain the shape of the profile. Alternatively, we present a linear inversion that can be used to directly solve for the unknown 4He distribution. The inversion incorporates a standard regularization technique to filter the influence of random measurement errors on the solution. Using either approach we show that stepwise degassing data can yield robust and high-resolution information on the 4He profile. Profiles of radiogenic He are a sensitive function of the time–Temperate (t–T) path that a cooling sample experienced. Thus, by step heating a proton-irradiated sample it is possible to restrict the sample’s acceptable t–T paths. The sensitivity of this approach was explored by forward-modeling 4He profiles resulting from a range of realistic t–T paths, using apatite as an example. Results indicate that 4He profiles provide rich information on t–T paths, especially when the profiles are coupled with (U–Th)/He cooling ages on the same sample. Samples that experienced only moderate diffusive loss have 4He concentration profiles that are rounded at the edge but uniform in the core of the diffusion domain. Such profiles can be identified by nearly invariant 4He/3He ratios after the first few to few tens of percent of 3He have been extracted by step heating. We show how such data can be used to correct (U–Th)/He ages for partial diffusive loss.  相似文献   

14.
We have studied two young speleothems, SC4 from Smiths Cave (Christmas Island, eastern Indian Ocean) and WM7 from Wollondilly Cave (Wombeyan caves, SE Australia). Attempts to date these speleothems by the Th/U method have proved unsuccessful with some age reversals for SC4 due to multiple sources of non-authigenic Th. This method has also resulted in imprecise ages for WM7 because of low U concentrations (<10 ppb) and consequently very low levels of authigenic 230Th relative even to the very low levels of detrital 230Th present. Here, we present an alternative method for reliable dating of these young speleothems using radiocarbon. Approximately 100 carbonate samples from SC4 and WM7 were analysed for 14C by accelerator mass spectrometry (AMS). The AMS results indicate that bomb 14C was evident in the youngest parts of both stalagmites. Two different approaches were used to estimate dead carbon fraction (DCF) values for these stalagmites for the pre-bomb period. For SC4, the DCF values were estimated based on the timing of 14C dates for that period determined by high-resolution δ18O recorded in the speleothem, and the timing of the onset of bomb 14C. For WM7, a “maximum” range of pre-bomb DCF was determined. Chronologies of these speleothems were built based on a dense sequence of DCF-corrected ages using three different age-depth models: Clam (Classical method), and Bacon and OxCal (Bayesian statistical approach). Good agreement between these age-depth models were observed indicating that the top 170 mm of SC4 and the top 50 mm of WM7 grew during the past 550–750 years and 1360–1740 years, respectively.  相似文献   

15.
We analyzed, U, Th and230Th/232Th activity ratios for a few tholeiites from the Mid-Atlantic Ridge FAMOUS zone at 36°50′N. The results show a fairly wide scatter for both Th/U and (230Th/232Th) ratios. Seawater contamination appears to be responsible for this scatter and, for the uranium, produces an increase in content yielding a (234U/238U) ratio greater than 1 and, for the Th, an increase of the (230Th/232Th) ratio which is a very sensitive indicator for contamination. Also, the latter often is selective: U, Th and Sr are not affected in the same manner.When discarding all data for contaminated samples, the FAMOUS zone appears to be very homogeneous with aTh/U ratio value of 3.05 and a (230Th/232Th) ratio value of 1.24. Comparison with other active volcanic areas reveals a negative correlation between (230Th/232Th) and87Sr/86Sr ratios for present lavas which is indicative of a consistency in Th-U and Rb-Sr fractionation in the source regions of these magmas. The Th isotopic geochemistry can thus provide useful information for the study of present volcanism, information as valuable as that from Sr, Pb or Nd isotopes.  相似文献   

16.
As one of the important deposit-clustered regionsof China, the Liaodong (eastern Liaoning Province)rift zone contains many large lead, zinc, gold, boron,magnesite and talc ore deposits with a long mininghistory. Recently, large-scale Xiaotongjiapuzi gold andGaojiapuzi silver deposits were discovered in the re-gion. Much work on the origin of these deposits hasbeen carried out, however, the discrepancy on the ageand the metal source of the deposits still rem- discu…  相似文献   

17.
K, Rb, Sr contents and Sr isotopic composition are reported for (1) the coexisting silicate minerals of a spinel lherzolite xenolith, (2) the whole rock xenolith, and (3) the host alkali basalt from the Pleistocene-Recent San Quintin volcanic field in Baja California. The data also include major element chemistry of the four mineral phases of the xenolith. The olivine-spinel and pyroxene thermometers indicate that the last temperature of equilibration of the xenolith in the upper mantle was about 1100°C.K, Rb, and Sr abundances are extremely low in the minerals of the xenolith, in contrast with the general enrichment of Ca, Al, Fe and Na in the whole xenolith. Furthermore, the abundance levels and the87Sr/86Sr ratios of the minerals are greatly lowered by surface washing of the minerals in2N cold HCl for three minutes. It is suggested that this is due to grain boundary and surface contamination of the minerals which took place in the upper mantle by a vapor phase deposition, prior to the inclusion of the xenolith in the basalt. The source of the vapor phase must have a87Sr/86Sr ratio greater than 0.7070, the highest measured ratio in the unwashed orthopyroxene. Sr in the host alkali basalt has a87Sr/86Sr ratio of 0.7031, unrelated to the grain boundary material.The acid-washed minerals, the unwashed minerals and the acid-washed whole rock xenolith show a scatter on a87Rb/86Sr versus87Sr/86Sr diagram. However, the surface-washed minerals and the whole rock alone define a straight-line relationship with a positive slope, which corresponds to an age3.4 ± 0.3AE(2σ) for the rock and an initial87Sr/86Sr of0.70057 ± 0.0004 (2σ). The age of 3.4 AE for the lherzolite is interpreted as its last involvement in a small degree of partial melting and the consequent extreme depletion of the large ion lithophile elements from the constituent minerals.  相似文献   

18.
In the loess plateau of China, the stratigraphical position of the Brunhes / Matuyama boundary was not found in loess unit L8 at Luochuan and Jixian as is commonly accepted. The interbedded palaeosols may be differentiated from the parent loess not only by their high magnetic susceptibility but also by their enhanced remanence properties. These contrasts mainly result from concentration changes of the inherited magnetic minerals, grain-size changes and authigenic formation of magnetic minerals, which are all linked to climate-controlled soil formation processes.  相似文献   

19.
The thorium isotope content of ocean water   总被引：1，自引：0，他引：1  
232Th concentrations of surface and deep Pacific Ocean waters are 0.01–0.02 dpm/1000 kg (60 pgm/kg). The230Th activity is 0.03–0.13 dpm/1000 kg in surface waters and 0.3–2.7 dpm/1000 kg in deep waters. Chemical residence times based on in situ production from parent isotopes are about the same for230Th and228Th in surface waters (1–5 years) but are ten times greater for230Th in deep waters (10–100 years). Apparently there are additional sources of230Th into deep waters. At MANOP site S manganese nodule tops are enriched in Th isotopes by adsorption of Th from seawater and not by incorporation of Th-rich particulates.  相似文献   

20.
Analyses of rock-magnetic properties of Neogene sediments of the Taxihe section, northern Tianshan Mountains, show that the section can be classified into three categories including lacustrine facies, fluvial facies and alluvial facies, which correspond to the lower, middle and upper of the Taxihe section respectively. The magnetic minerals of the lacustrine facies may be affected by the process of weath- ering, lithogenesis and biolithogenesis besides the source of the sediments. The natural remanence intensities are between 10-3 A/m and 10-2 A/m. The minerals are dominated by magnetite and the high coercive magnetic mineral may be goethite. The magnetic grains are the mixture of PSD SD or SD SP. The natural remanence intensities of the strata of fluvial facies are between 10-2 A/m and 10-1 A/m, about ten times that of the lacustrine facies. The magnetic minerals are mainly magnetite and hematite, and the magnetic grains are mainly PSD. The characteristic remanence (ChRM) carriers are magnetites. In the alluvial facies, the natural remanence intensities are mostly less than 1×10-2 A/m. The magnetic minerals of the series are dominated by magnetite and hematite, almost the same as the fluvial facies. But the difference is that most of the stepwise demagnetization can reveal two components and the ChRM carriers are hematites. The magnetic grains are PSD in terms of the hysteresis parameters.  相似文献   

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