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1.
The capacity of mine waste to trap CO2 is, in some cases, much larger than the greenhouse gas production of a mining operation. In mine tailings, the presence of secondary carbonate minerals that trap CO2 can therefore represent substantial fixation of this greenhouse gas. The abilities of three methods of quantitative phase analysis to measure trace nesquehonite (MgCO3·3H2O) in samples of processed kimberlite have been assessed: the method of reference intensity ratios (RIR), the internal standard method, and the Rietveld method with X-ray powder diffraction data. Tests on synthetic mixtures made to resemble processed kimberlite indicate that both the RIR and Rietveld methods can be used accurately to quantify nesquehonite to a lower limit of approximately 0.5 wt.% for conditions used in the laboratory. Below this value, estimates can be made to a limit of approximately 0.1 wt.% using a calibration curve according to the internal standard method. The RIR method becomes increasingly unreliable with decreasing abundance of nesquehonite, primarily as a result of an unpredictable decline in preferred orientation of crystallites. For Rietveld refinements, structureless pattern fitting was used to account for planar disorder in lizardite by considering it as an amorphous phase. Rietveld refinement of data collected from specimens that were serrated to minimize preferred orientation of crystallites gives rise to systematic overestimates of refined abundances for lizardite and underestimates for other phases. The resulting pattern of misestimates may be mistaken for the effect of amorphous and/or nanocrystalline material in samples. This effect is mitigated by collecting data from non-serrated specimens, which typically give relative errors on refined abundances for major and minor phases in the range of 5–20%. However, relative error can increase rapidly for abundances less than 5 wt.%. Nonetheless, absolute errors are sufficiently small that estimates can be made for the amount of CO2 stored in secondary nesquehonite using the RIR method or the Rietveld method for abundances ?0.5 wt.% and a calibration curve for abundances <0.5 wt.%. The extent to which C is being mineralized in an active mine setting at the Diavik Diamond Mine, Northwest Territories, Canada, has been investigated. Rietveld refinement results and calibrated abundances for trace nesquehonite are used to estimate the amount of CO2 trapped in Diavik tailings. Results of quantitative phase analysis are also used to calculate neutralization potentials for the kimberlite mine tailings and to estimate the contribution made by secondary nesquehonite.  相似文献   

2.
Fluid and solid inclusions have been studied in selected samples from a series of spinel-bearing Crdiopside-and Al-augite-series ultramafic (harzburgites, lherzolites, and olivine-clinopyroxene-rich rocks), and gabbroic xenoliths from Hierro, Canary Islands. In these samples several generations of fluid inclusions and ultramafic-and mafic-glass inclusions may be texturally related to different stages of crystal growth. The fluid inclusions consist of pure, or almost pure, CO2. The solid inclusions in the ultramafic xenoliths comprise early inclusions of devitrified ultramafic glass, sulphide inclusions, as well as polyphase inclusions (spinel+clinopyroxene±glass±other silicates) believed to have formed from trapped basaltic melts. Vitreous basaltic glass±CO2±sulphide±silicates are common as secondary inclusions in the ultramafic xenoliths, and as primary inclusions in the gabbroic xenoliths. Microthermometry gives minimum trapping temperatures of 1110° C for the early ultramafic-and mafic-glass inclusions, and a maximum of 1260–1280° C for late inclusions of host basaltic glass. In most samples the CO2 inclusions show a wide range in homogenization temperatures (-40 to +31° C) as a result of decrepitation during ascent. The lowest homogenization temperatures of about-40° C, recorded in some of the smallest CO2 inclusions, indicate a minimum depth of origin of 35 km (12 kbar) for both the Cr-diopside-and Al-augite-series xenoliths. The gabbroic xenoliths originate from a former magma chamber at a depth of 6–12 km.Contribution no. 100 of the Norwegian programme of the International Lithosphere Project  相似文献   

3.
Summary Pyroclastites erupted from the Upper Pollara magma chamber (13 ka, Salina Island, Aeolian Archipelago) resulted from mingling and mixing of rhyolitic and andesitic magmas. An experimental study has been conducted on the rhyolitic end-member to constrain the pre-eruptive conditions of the magma. In order to check for the role of mixing on the equilibrium phase assemblage, three different starting compositions, corresponding to three different mixing degrees, have been used. The crystallization experiments were conducted at two different oxygen fugacities and at variable temperature and fluid contents. The results indicate that the natural mineralogical assemblage can only be reproduced from a composition showing a certain degree of mixing. Assuming a pressure of 200 MPa (generally accepted for the Aeolian Islands), the pre-eruptive temperature of the magmas is estimated between 755 and 800 °C and the water content of the melt was higher than 4–4.5 wt.%. The Upper Pollara magma crystallized at relatively high fO2 (ΔlogfO2 = Ni–NiO + 1 log unit), compared to rhyolitic magmas from Lipari and Vulcano. As this difference has not been observed for the most primitive magmas the difference in fO2 could be related to different degassing processes operating in Salina and Lipari – Vulcano magmas.  相似文献   

4.
Ca2SiO4 dicalcium silicate has been transformed at high pressure in a diamond-anvil cell (DAC) coupled with a YAG laser heater, in order to study the high-pressure modifications of this compound. Starting material was the olivine form of Ca2SiO4 (γ-polymorph). Several samples have been synthesized at loading pressures of 4.5, 10 and 15 GPa respectively, at room temperature. Other samples have been obtained at pressures ranging between 4.5 and 45 GPa and temperatures estimated to be about 2500 °C. The study of the quenched high pressure and/or high temperature phases has been performed using analytical transmission electron microscopy (ATEM) and X-ray diffraction (XRD). All the polymorphs of Ca2SiO4 usually produced with high temperatures, including α-Ca2SiO4, have been observed in the samples recovered from the high-pressure experiments. The α′-Ca2SiO4 and α-Ca2SiO4 polymorphs have been obtained at ambient conditions for the first time without stabilizing impurities. A new modification of α′-Ca2SiO4 has also been synthesized. Finally, the breakdown at high-pressure and temperature of Ca2SiO4 into CaSiO3 and CaO is reported.  相似文献   

5.
Based on the experiments on dehydration-melting of solid samples of Al-rich gneiss (H029) and biotite granulitite (H013), the fugacities of O2, H2O and H2 have been calculated. It is recognized that the fugacities of O2, H2O and H2 vary regularly, but the fugacity of H2O shows a tendency of abrupt increasing at about 700°C and 800°C. According to the above fact, the melting mechanism of biotite can be well documented. Under relatively low temperatures (< 750°C), part of the water can be liberated and induce plagioclase to melt, which may mark the beginning of migmatization. At high temperatures (> 800°C), biotite can be dissociated and a larger amount of water can be released, which would result in a bigger degree of melting, hence leading to the formation of granitic magma.  相似文献   

6.
 More than 5 800 chemical analyses on water samples collected during 1987–1995 from 528 monitoring wells located in the southernmost part of the Po Valley (Emilia-Romagna region, northern Italy), one of the most urbanized, industrialized and agriculturally developed areas of Italy, have been processed. The analysis of data showed that: (1) waters are discharging from both confined and unconfined aquifers; (2) the water in the unconfined aquifer(s) is Ca(Mg)-HCO3 in composition while confined ones are Na-Cl and/or Na-(HCO3); (3) both confined and unconfined aquifer samples have δ18O and δD isotopic values of meteoric signature; (4) waters from both the aquifers are at least 40 years old; (5) the pumping rate has caused subsidence, particularly where the aquifer(s) is (are) unconfined; (6) the unconfined aquifer(s) is exposed to the risk of NO3 pollution; (7) considering the present "pressure" (i.e. pumping rate) on this natural environment by human activity, care must be taken in the future to preserve this "strategic" resource. Received: 27 October 1997 · Accepted: 12 March 1998  相似文献   

7.
A new digestion procedure and chemical separation technique has been developed for measurement of Lu/Hf and Hf isotope ratios that does not require high‐pressure bombs or use of HF or HClO4 acids. Samples are digested in dilute HCl or HNO3 after flux‐fusion at 110 0 °C in the presence of lithium metaborate. High field strength elements (HFSE) and rare earth elements (REE) are separated from this solution by co‐precipitation with iron hydroxide. The dissolved precipitate (in 2 mol l?1 HCl) is loaded directly onto a standard cation exchange column which separates remaining sample matrix from the heavy REE (Lu+Yb), and the middle‐light REE and HFSE (Hf). The middle‐light REE and individual HFSE are then separated (10.5, 9 and 6 mol l?1 HCl) using a miniaturized column containing TEVA spec resin which provides a REE‐, Ti‐ and Zr‐free Hf cut. This chemical separation scheme can also be readily adapted for isotopic analysis of the Sm‐Nd system and/or the other HFSE (Ti, Zr). Total procedural blanks for this technique are < 10 0 pg and < 2 pg for Hf and Lu, respectively, even when digesting large (0.5 g) samples. We present data from replicate digestions of international rock reference materials which demonstrate this technique routinely reproduces Lu/Hf ratios to < 0.2% (2s) and 176 Hf/177 Hf isotope ratios to < 30 ppm (2s). Moreover, the technique is matrix‐independent and has been successfully applied to analysis of diverse materials including basalts, meteorites, komatiites, kimberlites and carbonatites. The relative simplicity of this technique, coupled with the ease of digestion (and sample‐spike equilibration) of large difficult‐to‐dissolve samples, and the speed (2 days) with which samples can be digested and processed through the chemical separation scheme makes it an attractive new method for preparing samples for Lu‐Hf isotopic investigation.  相似文献   

8.
Compressional (VP) and shear (VS) wave velocities and the dependent elastic constants have been determined by the pulse transmission technique to 6 kb confining pressure at room temperature and to 700° C at 6 kb confining pressure for eleven basalts from the Faeroe Islands. The Faeroe basalts investigated are tholeiitic, they clearly lie within the tholeiitic area, and display a pronounced trend of iron enrichment from rocks with an M/M + F ratio of 0.5 to rocks with an M/M + F ratio of about 0.25. The mean VP and VS for eleven specimens are 5.57 km/sec and 3.18 km/sec, respectively. Velocity—density relations for the basalts might be more appropriately described by non-linear solutions than by linear relations commonly used for basalts. In general, VP and VS remain unaffected by temperature up to 300° C. At higher temperature the changes in wave velocities are influenced by metamorphic processes and are, therefore, somewhat erratic. In zeolite-bearing specimens an abrupt velocity decrease around 350°C is observed, which correlates well with a drastic compaction of bulk volume. Additional experiments on cold-pressed zeolite powder clearly indicate that the sharp velocity decrease in the basalts is related to dehydration of zeolite minerals. Partial-melting processes, which occur within vesicules and pore-spaces at distinctly higher temperatures have no additional effect on wave velocity. Comparison with field data reveals that, without exception, the velocities at 0.5 kb confining pressure display the same range that has been commonly noted in refraction data for Layer 2. There are no significant differences in wave velocities and the pressure—temperature dependence in samples recovered from the upper, middle, and lower basalt series in the Faeroe Islands.  相似文献   

9.
Fluid inclusions, ranging from pure N2 to pure CO2, occur in olivine porphyroclasts in spinel dunite xenoliths (chrome-diopside suite) from two localities within the Quaternary to Historic alkaline lavas of Lanzarote, Canary Islands. This is the first report of fluid inclusions containing major amounts of N2 in mantle xenoliths. The nitrogen-rich fluid inclusions predate at least one generation of nitrogen-free carbon dioxide inclusions; textural evidence indicates that the inclusions were trapped within the upper mantle. Some of the nitrogen-rich fluid inclusions are intimately associated with solid inclusions of spinel. The nitrogen-rich fluid was most likely produced in-situ, by oxidation-dehydration reactions destabilizing ammonium-bearing silicate minerals (phlogopite, amphibole), increasing oxygen fugacity or, possibly, increasing temperature of the mantle. This process could be related to an event of CO2 and silicate melt injection at 6–8 kbar (Neumann et al., in press), or to some earlier event in the evolution of the mantle beneath Lanzarote. The existence of a N2-rich fluid phase in at least some mantle lithology(ies) at certain conditions is demonstrated by these data. This discovery has consequences for the understanding of the evolution of the mantle below the Canary Islands, as well as for the global nitrogen budget.  相似文献   

10.
The Lovozero pluton (Kola Peninsula, Russia) is an unique object from the standpoint of the abundance, diversity, and originality of Th mineralization. In contrast to other igneous rocks and to such chemical elements as Ca, REE, U, and Na, Th in the hyperalkaline pegmatites and hydrothermalites of the Lovozero pluton commonly occurs as its own mineral phases. Umbozerite Na3Sr4Th(Mn,Zn,Fe,Mg)[Si8O24](OH) (7 samples), Ti-Th silicate Na0–7Sr0–1ThTi1–2Si8O22–23(OH) · nH2O (8 samples), Na-Th silicate (Na,K)4Th3[Si8(O,OH)24] · nH2O (6 samples), thorite (2 samples), steenstrupine-(Ce)-thorosteenstrupine series minerals (5 samples), and Th phosphate (Th,Na,K,Ca,Mg,U,Sr,Ba)[(P,Si, Al)1O4] · nH2O (1 sample) were investigated in this study. Ti-Th silicates and Th phosphate have been described for the first time. All of the above-mentioned minerals have been examined with electron microprobe, IR spectroscopy, powder diffraction, thermogravimetric and optical methods. High-Th minerals such as steenstrupine, umbozerite, Th phosphate, and Na-Th silicates crystallized mainly during the ussingite stage of the pegmatite-forming process. At the early hydrothermal high-alkaline stage, steenstrupine was replaced with REE and Th aggregates (belovite, vitusite, seidite, Na-Th silicates, Ti-Th silicates, etc.). Thorite, Ti-Th silicates, and minerals of the rhabdophane and monazite groups were formed at the late hydrothermal low-alkaline stage. Despite the metamict features of almost all samples, stoichiometric ratios of cations in umbozerites and Ti-Th silicates remain stable. Clear relationships have been revealed between umbozerites and Ti-Th silicates, on the one hand, and seidite-(Ce), a Ti-silicate that has a zeolite-like structure, on the other. This implies that, under certain conditions, these minerals may be regarded as potential suppliers of Th to the environment due to the leaching of Th from zeolite channels.  相似文献   

11.
Gabbro xenoliths reported in this paper were collected in northern Fuerteventura, the Canary Island located closest to the coast of Africa. The xenoliths are very fresh and consist of Ti–Al-poor clinopyroxene + plagioclase (An87–67) + olivine (Fo72–86) ± orthopyroxene. Clinopyroxene and orthopyroxene are constantly and markedly depleted in light rare earth elements (LREE) relative to heavy REE (HREE), as expected for cumulus minerals formed from highly refractory N-MORB-type melts. In contrast, whole-rock Primordial Mantle-normalized trace element patterns range from mildly S-shaped (mildly depleted in Pr–Sm relative to both the strongly incompatible elements Rb–La and the HREE) to enriched. Estimates show that the trace element compositions of the rocks and their minerals are compatible with formation as N-MORB gabbro cumulates, which have been infiltrated at various extents (≤1% to >5%) by enriched alkali basaltic melts. The enriched material is mainly concentrated along grain boundaries and cracks through mineral grains, suggesting that the infiltration is relatively recent, and is thus associated with the Canary Islands magmatism. Our data contradict the hypothesis that a mantle plume was present in this area during the opening of the Atlantic Ocean. No evidence of continental material that might reflect attenuated continental crust in the area has been found. Gabbro xenoliths with REE and trace element compositions similar to those exhibited by the Fuerteventura gabbros are also found among gabbro xenoliths from the islands of La Palma (western Canary Islands) and Lanzarote. The compositions of the most depleted samples from these islands are closely similar, implying that there was no significant change in chemistry during the early stages of formation of the Atlantic oceanic crust in this area. Strongly depleted gabbros similar to those collected in Fuerteventura have also been retrieved in the MARK area along the central Mid-Atlantic Ridge. The presence of N-MORB oceanic crust beneath Fuerteventura implies that the continent–ocean transition in the Canary Islands area must be relatively sharp, in contrast to the situation both further north along the coast of Morocco, and along the Iberian peninsula.  相似文献   

12.
Twenty-nine dug well samples have been collected from the Gambhir River basin in the Bharatpur District of Rajasthan State in India for hydrogeochemical study to understand the sources of dissolved ions and assess the chemical quality of the water. Broadly speaking, the groundwaters have a chemical composition within the permissible limits suggested for drinking water. Nitrate is higher than the acceptable limit in some samples, due to the use of fertilizers. Graphical treatment of the major ion chemistry helps in deciphering the chemical characteristics of groundwaters, which may then be used for grouping the samples to identify the trends of the chemical alteration of the meteoric water. Four groups have been identified in the Gambhir River basin groundwater system: (1) HCO 3 enriched, (2) mixed type, (3) alkali-rich, high TDS type, and (4) HCO 3 deficient. Possible aqueous species have been identified for these four groups of samples. In groups I and II, the species are Ca (HCO 3) 2, Mg (HCO 3) 2, NaCl, Na 2SO 4 and NaHCO 3. Group III, in addition to these species, has abundance of KCl. Group IV has Ca (HCO 3) 2, NaCl, CaSO 4, and rather rare species such as CaCl 2, MgCl 2 and MgSO 4. Interpretation of the data reveals that feldspar and pyrite weathering reactions do not play a significant role in giving groundwaters their observed chemical characteristics. Groups I and II samples have evidently been derived by dissolution of surface salts, whereas groups III and IV groundwaters suggest dissolution of a marine evaporite sequence similar to the one known to exist to the west of the study area, unconformably overlying the rocks of the Delhi Super Group. There are indications that joints play an important role in segregating groundwaters with different chemical characteristics.  相似文献   

13.
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14.
Fullerenes have been detected in carbonaceous chondrite meteorites and in breccia samples from meteorite impact craters, but questions have been raised about contradictory results from similar samples and the sensitivities and accuracies of different analytical methods. We analyzed samples from three impact craters and detected C60 in samples from several locations; we also observed differences in the detection capabilities of various analytical techniques used in the search for fullerenes. The presence of C60 in rocks from the Onaping Formation of the Sudbury impact crater was confirmed. Low levels of C60 were also detected for the first time in samples from the Gardnos (Norway) and Ries (Germany) impact structures.We detected C60 in these samples using surface-enhanced laser desorption/ ionization (SELDI), but the related technique of microprobe laser-desorption, laser-ionization mass spectrometry (μL2MS) did not observe C60 above detection limits. We attribute the absence of μL2MS signal to aggregate formation caused by phthalic acid esters, which appear to easily contaminate samples either during storage or demineralization in plastic containers. The μL2MS technique is incapable of detecting aggregated C60, but aggregation does not suppress detection in SELDI. Phthalate-induced aggregation did, however, enhance SELDI detection of C60 in some cases, and we suggest that this enhancement may help explain previously reported differences in C60 detection from natural samples between laser desorption mass spectrometry (LDMS, a technique analogous to SELDI that has detected fullerenes in meteorite and impact breccia samples) and high-pressure liquid chromatography (HPLC). This work highlights the effects of phthalates and other indigenous compounds or contaminants on certain mass spectrometric techniques and lends support to the idea that several complementary analytical methods should be employed to investigate complex natural samples.  相似文献   

15.
采用氢化物发生技术测定地质样品中的硒时,需要考虑样品的溶解、Se价态的预还原以及抑制共存离子的干扰。本文采用硝酸-盐酸-氢氟酸-高氯酸体系快速溶解样品,直接加入浓盐酸煮沸将六价硒还原为四价硒,将氢化物发生器与电感耦合等离子体发射光谱仪联用测定了铀矿地质样品中的痕量硒。样品中除了Cu2+其他离子的含量均不干扰硒的测定,通过在试液中加入铁盐溶液或在硼氢化钠还原剂中加入铁氰化钾抑制了Cu2+的干扰。方法检出限为0.12μg/L,精密度(RSD)小于5%。与前人报道的方法相比,本方法检出限较低,操作简单快速,冲洗30 s可消除记忆效应,适合批量铀矿地质样品中痕量硒的测定。  相似文献   

16.
《Applied Geochemistry》1997,12(3):267-280
The SiO2 contents of landfill leachates have been monitored (together with other constituents) for up to 21 sampling locations at 3 landfill sites in Cheshire, England, at 6 month intervals over a 2 a period. The observed SiO2 values average 26.9 mg/l SiO2 (s.d. 12.1 mg/1), and show no variation that can be attributed to the transition from acetogenesis to methanogenesis. The youngest (<2 a) leachates have highest SiO2 levels (27–47 mg/I). Geochemical modelling shows that most samples are supersaturated with respect to both quartz and chalcedony, and with respect to calcite. Ion activity diagrams suggest that alkali and SiO2 activities are controlled by reactions which involve clay minerals, especially smectites, probably as constituents of the waste rather than the site containment. Ammonium also appears to be controlled by exchange with K within clays. The information gained in this study suggests that SiO2 should be routinely determined for leachates, to permit a more detailed interpretation of the processes and reactions that influence their compositions.  相似文献   

17.
The efficiency of neutron activation as an analytical technique has been evaluated for exploration of lateritic and karstic bauxites in Sierra Leone, Guinea, Australia (Gove), Philippines and Jamaica. The 10-g bauxite samples are prepared in the field and sent to a central laboratory. With the “Automatic Bauxite Analyzer” — equipped with an isotopic neutron source — a single Al and Si determination can be made in 5 minutes. For calibration, standards are required which are similar in composition to the samples to be analyzed. Using sample pairs and averaging the results of three subsequent determinations an accuracy of ±2% Al2 O3 and about ±0.6% SiO2 can be obtained. Time requirements, accuracy and cost of this technique are compared with wet chemistry and X-ray fluorescence. For an exploration programme incorporating for example 15,000 drill core samples, a 50% reduction in expenditure for analytic determinations can be achieved by applying neutron activation instead of X-ray fluorescence alone.  相似文献   

18.
We report new stepped heating He, Ar, CO2 and water data on a petrogenetically diverse suite of lavas from the Manus back-arc basin, where a plume component has previously been identified. The aim of this study is to evaluate the superimposed effects of degassing and contamination in order to identify mantle source characteristics. CO2 abundances and carbon isotopes in both the vesicle ([CO2] up to 180ppm; δ13C as low as -33.6 ‰) and glass ([CO2] up to 270ppm; δ13C as low as -34.3 ‰) phases reveal that samples have been modified by varying degrees of degassing. High water concentration samples (back-arc basin basalts (BABB) and arc type samples) show the highest degrees of degassing (i.e. lower δ13C values and lower CO2 contents). The results are modelled for both the glass and vesicle phases using batch and fractional degassing models. Parental melt compositions can be constrained to show the following CO2 concentration trend: arc-type > BABB s.r. (southern rift) > MORB-2, E-MORB, X-BABB (extreme BABB), BABB > MORB-1 and MORB-smt. 4He/40Ar∗ ratios of samples (14.6-1100) are consistent with residual volatiles from a degassed source. Variations in CO2/3He values are likely due to degassing, followed by contamination from a crustal source (either the subducting Solomon Sea Plate or the pre-existing crust through which the lavas erupt), as evidenced by high K2O/TiO2 ratios and low δ13C. The CO2/3He of the Manus plume is best estimated by the MORB-smt and MORB-1 samples at 3.1 ± 0.6 x 109. This value is similar to previous estimates of plume CO2/3He values, which are either equal to or slightly greater than the upper mantle average of 2 x 109.  相似文献   

19.
南海全新世大暖期海表水的高酸性证据   总被引：1，自引：1，他引：0       下载免费PDF全文
利用正热电离质谱高精度测定了南海化石珊瑚样品的δ11B 比值,定量地重建了中晚全新世以来南海海表水的pH值。结果显示南海海表水pH值并不像预先设想的那样稳定。其中古海水pH值最低为6100aB.P.前的7.91;   最高为4300aB.P.前和1200aB.P.前的8.29。南海海表水pH值从全新世大暖期开始,整体上呈缓慢增加趋势,而到现代以后明显下降。珊瑚δ11B记录表明南海海表水在中晚全新世有两个高酸性的时期,一个发生在全新世大暖期,一个为现代。全新世大暖期时南海出现的高海平面、偏强的东亚夏季风和偏弱的冬季风可能是导致其海表水出现高酸性的原因。现代南海海表水pH值显著偏低,背离了中晚全新世以来南海海表水pH值逐渐增加的趋势,这很可能说明人类大量排放的CO2确实改变了南海海表水自然变化的规律,南海在变酸。  相似文献   

20.
44 samples of the Jilin meteorite were analyzed by various laboratories for spallogenic, radiogenic, and trapped rare gases. A non-uniform distribution has been found for the rare gases of different origins. There have been found correlations among the spallogenic rare gases, with apparent depth effects. 43 samples were analyzed for their cosmogenic radionuclides60Co,26Al,36Cl,40K,53Mn,54Mn, and22Na. Correlations have been found between60Co and53Mn and between60Co and21Ne. The Jilin meteorite has a complex history of cosmic-ray irradiation. According to the two-stage model and the other fragments have a burying depth two stages,T 1=11 m.y. andT 2=0.3 m.y. The burying depth of all samples in the parent body can be obtained by the content of21Ne. Jilin meteorite No. 1 is located 20–142 cm from the surface, No. 4 ranges from 106–134 cm, and the other fragments have a burying depth between 15 and 150 cm. The equation of the reference plane for the surface of the 1-stage Jilin meteoroid is 0.24x+0.81y+0.53z+0.5=0. Use can also be made of60Co to determine the burying depth of all samples in the 2-stage Jilin meteoroid (under a geometry of 4π), and further to restore the preatmospheric form and size of the parent body. During its atmospheric passage, the Jilin had an ablation rate of ca. 30%. On the basis of the two-stage model and the concentration of21Ne and60Co in the samples, we propose a scheme to restore the relative position of all samples in the parent body. 12 sample-distribution regions can be sketched out. Also can be restored the relative position of all the samples in the parent body during the two stages.  相似文献   

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