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1.
赣南横径地区碳酸温泉CO2成因研究 总被引：1，自引：0，他引：1
本文在分析横径温泉区4个气样的气体组分、氦同位素以及CO2和CH4的碳同位素基础上,结合温泉区地质条件,研究了该区碳酸温泉中CO2的成因。研究结果表明:横径温泉区温泉气中CO2的含量很高(>96%),CO2气体中1δ3C较重(-5.53‰~-4.43‰),属于与深大断裂活动有关的深部幔源无机成因气;温泉气中CH4的含量很低(<1.86%),CH4气体中1δ3C较轻(-27.69‰~-59.31‰),其中39、和11号温泉气体中的CH4属于深部幔源无机CH4和源于地表生物成因CH4的混合,而2号温泉气体中的CH4属于深部幔源无机CH4。 相似文献
2.
石灰稳定红黏土强度的长期碳化效应 总被引：1，自引：0，他引：1
碳化效应是石灰稳定土强度增长机理之一,但长期的碳化作用是否对其强度一直起促进作用？如果没有压实作用,碳化效果到底如何？这些关键问题还没有得到充分的论证。采用灰土拌和后击实养护和养护后再击实的不同制样方法,通过承载比CBR试验,探讨压实作用对碳化效应的影响。制备4种初始含水率的击实试样,开展碳酸溶液和纯水浸泡下的CBR试验,论证长期碳化对石灰稳定土强度的作用效果。结果表明,自然养护90 d后再击实试样的CBR值明显低于击实后养护的试样;初始含水率为34%时前者约为后者的12倍。另外,碳酸溶液浸泡15 d后的试样CBR值均小于纯水浸泡的试样CBR值,但初始含水率越大其影响程度越小,当初始含水率大于34%后两者之间的强度基本没有差别。为进一步佐证长期碳化作用能弱化石灰稳定土的强度,开展不同浸泡时间的无侧限抗压强度试验,发现石灰土的强度呈现先增大后减少的变化趋势,再次证实长期的碳化作用弱化石灰稳定土的强度。最后,利用热重分析法测试经过碳酸溶液浸泡前后的石灰稳定土,发现长期碳化溶解了部分石灰土中的碳酸钙和硅酸盐类胶结物。借助扫描电镜图片和孔隙尺寸分布曲线,从微观角度揭示不同击实和养护方式对石灰稳定土强度的影响机制。 相似文献
3.
地壳再循环与大陆碱性玄武岩的成因：以山东新生代碱性玄武岩为例 总被引：6，自引：0，他引：6
大陆碱性玄武岩在地球化学特征上与洋岛玄武岩高度相似,被看做是板内玄武岩在大陆上的典型代表。本文以山东
新生代碱性玄武岩为例,探讨大陆碱性玄武岩的成因。山东新生代碱性玄武岩按时空分布特征可以分为两类：早期定向分
布、相互平行的三个火山群（包括鲁西的潍坊火山群、沂水火山群和胶东的蓬莱火山群）和晚期杂乱分布的孤立小火山。
早期火山群碱性较弱,以碱性橄榄玄武岩和碧玄岩为主,微量元素特征和同位素组成变化大;晚期孤立小火山碱性强,以
碧玄岩和霞石岩为主,微量元素特征和同位素组成较均一。因此,从岩性组成和时空分布特征看,山东的火山群相当于洋
岛/海山的造盾期玄武岩,而孤立小火山接近于洋岛/海山上的复苏期玄武岩。潍坊火山群和沂水火山群在Sr-Nd,Nd-Hf同位
素相关图上都存在从亏损到富集的两端元混合排列趋势,但两者的排列趋势有一点区别。其中同位素富集的端元相对于原
始地幔具有偏低的Ce/Pb比和偏高的Ba/Th比,指示其为大陆下地壳物质。同时,这种富集端元的Th/La比值明显低于大陆下
地壳的平均值,其放射成因Hf相对于放射成因Nd过剩（即Nd-Hf同位素解耦）,说明这种富集端元不是岩浆上升过程中混染
的下地壳物质,而是经历过早期熔融的再循环大陆下地壳（榴辉岩或者石榴辉石岩）。鲁西两个平行火山群在同位素排列上
的区别类似于夏威夷玄武岩中的KEA链和LOA链,因此,山东的平行火山群的深部动力学背景可能是地幔柱,再循环大陆
下地壳物质可能是这种地幔柱的重要组成物质。晚期的孤立小火山在地球化学特征上与火成碳酸岩非常相似,如在原始地
幔标准化图上都具有K,Pb,Zr,Hf,Ti的负异常等特征,因此我们认为其地幔源区为碳酸盐化的橄榄岩。孤立小火山中等亏损
的Sr,Nd,Hf同位素特征支持碳酸岩熔体来自年轻的（中生代？）再循环洋壳。 相似文献
4.
《International Geology Review》2012,54(11):1350-1362
ABSTRACTRecent studies show that crustal carbonates recycled into the mantle can be traced using Mg isotopes of basalts. However, the species of recycled carbonates are poorly constrained. Carbonates have lower δ26Mg values and higher 87Sr/86Sr ratios relative to the mantle, but different carbonate species display different mixing curves with the mantle in the Mg-Sr isotopic diagram because of differences in their Sr and Mg contents. Thus a combined study of Mg-Sr isotopes can constrain the species of deeply recycled carbonates. Here, we present newly determined 87Sr/86Sr ratios of the <110 Ma basalts from Eastern China, and together with published Mg isotopic data we evaluate the species of recycled carbonates in the mantle and discuss their implication. The <110 Ma basalts display low δ26Mg values of ?0.60 to ?0.30‰ and relatively low initial 87Sr/86Sr ratios of 0.70328 to 0.70537, suggesting that their mantle source was hybridized by recycled carbonates with a light Mg isotopic composition which had more significant effects on Mg than Sr isotope ratios. Mg-Sr isotopic data indicate that the recycled carbonates consist of magnesite and aragonite, but the possibility of calcite and dolomite cannot be eliminated. Based on the carbonated peridotite solidus, the equilibrium line between dolomite and magnesite + aragonite, as well as the mantle adiabat, the initial melting depth of the carbonated mantle, the source region of the studied basalts, was constrained at ~300–360 km. Thus, the subducted depth of the west Pacific slab underlying the carbonated mantle and supplying recycled carbonates should be greater than ~300–360 km, consistent with the seismic tomography result that the west Pacific slab now stagnates in the mantle transition zone. 相似文献
5.
The exceptional andalusite–kyanite–andalusite sequence occurs in Al‐rich graphitic slates in a narrow pelite belt on the hangingwall of a ductile normal fault in NW Variscan Iberia. Early chiastolite is replaced by Ky–Ms–Pg aggregates, which are overgrown by pleochroic andalusite near granites intruded along the fault. Slates plot in AKFM above the chloritoid‐chlorite tie‐line. Their P–T grids are modelled with Thermocalc v2.7 and the 1998 databases in the NaKFMASH and KFMASH systems. The univariant reaction Ctd + And/Ky = St + Chl + Qtz + H2O ends at progressively lower pressure as F/FM increases and A/AFM decreases, shrinking the assemblage Cld–Ky–Chl, and opening a chlorite‐free Cld–Ky trivariant field on the low temperature reaction side. This modelling matches the observed absence of chlorite in high F/FM rocks, which is restricted to low pressure in the andalusite stability field. The P–T path deduced from modelling shows a first prograde event in the andalusite field followed by retrogression into the kyanite field, most likely coupled with a slight pressure increase. The final prograde evolution into the andalusite field can be explained by two different prograde paths. Granite intrusion caused the first prograde part of the path with andalusite growth. The subsequent thermal relaxation, together with aH2O decrease, generated the retrograde andalusite–kyanite transformation, plus chlorite consumption and chloritoid growth. This transformation could have been related to folding in the beginning, and aided later by downthrowing due to normal faulting. Heat supplied by syntectonic granite intrusion explains the isobaric part of the path in the late stages of evolution, causing the prograde andalusite growth after the assemblage St–Ky–Chl. Near postectonic granites, a prograde path with pressure decrease originated the assemblage St–And–Chl. 相似文献
6.
将音频大地电磁测深法（AMT）应用于五大连池地区的碳酸矿泉水勘查,以Occam（奥克姆）方法进行数据反演,揭示了研究区域深部电性特征,结果与地质资料的解释一致。研究区内实测三个AMT剖面的反演结果均显示,该区域深部存在多条明显的断裂带,其深度超过-2.5 km,走向北西,规模不一。这些深部断裂可能是CO2气体向上运移的通道,由此可以推断CO2储气层,并为最终圈定碳酸矿泉水范围提供依据。 相似文献
7.
The Witwatersrand goldfields contain abundant assemblages that include pyrophyllite, chloritoid, chlorite, kaolinite and/or kyanite, with quartz. A chemographic analysis of the system Fe(Mg)-Al-Si-O-H involving these minerals yields 22 potential phase diagrams. Using orientation criteria and thermodynamic calculations as further constraints, this list has been reduced to three possible diagrams. New thermodynamic data favour one of these in particular.
This chemographic analysis demonstrates that formation of chloritoid is not restricted to the breakdown reaction of kaolinite plus chlorite in the F(M)ASH system, as stated by previous studies, but could be from pyrophyllite + chlorite → chloritoid + quartz + H2 O.
The metamorphic temperature variation between Witwatersrand goldfields exceeded 65 C, based on chlorite and chloritoid compositions. The lower and upper pressure limits are constrained by the andalusite to kyanite, and the sudoite/chlorite to carpholite boundaries, i.e. 1.5–2.8, and 7 kbar, respectively. The widespread pyrophyllite, chlorite and Fe-chloritoid in all the Witwatersrand goldfields, and the local occurrence of sudoite indicate a consistent low-pressure environment in which Mg-chloritoid would not be stable. 相似文献
This chemographic analysis demonstrates that formation of chloritoid is not restricted to the breakdown reaction of kaolinite plus chlorite in the F(M)ASH system, as stated by previous studies, but could be from pyrophyllite + chlorite → chloritoid + quartz + H
The metamorphic temperature variation between Witwatersrand goldfields exceeded 65 C, based on chlorite and chloritoid compositions. The lower and upper pressure limits are constrained by the andalusite to kyanite, and the sudoite/chlorite to carpholite boundaries, i.e. 1.5–2.8, and 7 kbar, respectively. The widespread pyrophyllite, chlorite and Fe-chloritoid in all the Witwatersrand goldfields, and the local occurrence of sudoite indicate a consistent low-pressure environment in which Mg-chloritoid would not be stable. 相似文献
8.
We explore the partial melting behavior of a carbonated silica-deficienteclogite (SLEC1; 5 wt % CO2) from experiments at 3 GPa and comparethe compositions of partial melts with those of alkalic andhighly alkalic oceanic island basalts (OIBs). The solidus islocated at 1050–1075 °C and the liquidus at 1415 °C.The sub-solidus assemblage consists of clinopyroxene, garnet,ilmenite, and calcio-dolomitic solid solution and the near solidusmelt is carbonatitic (<2 wt % SiO2, <1 wt % Al2O3, and<0·1 wt % TiO2). Beginning at 1225 °C, a stronglysilica-undersaturated silicate melt (34–43 wt % SiO2)with high TiO2 (up to 19 wt %) coexists with carbonate-richmelt (<5 wt % SiO2). The first appearance of carbonated silicatemelt is 100 °C cooler than the expected solidus of CO2-freeeclogite. In contrast to the continuous transition from carbonateto silicate melts observed experimentally in peridotite + CO2systems, carbonate and silicate melt coexist over a wide temperatureinterval for partial melting of SLEC1 carbonated eclogite at3 GPa. Silicate melts generated from SLEC1, especially at highmelt fraction (>20 wt %), may be plausible sources or contributingcomponents to melilitites and melilititic nephelinites fromoceanic provinces, as they have strong compositional similaritiesincluding their SiO2, FeO*, MgO, CaO, TiO2 and Na2O contents,and CaO/Al2O3 ratios. Carbonated silicate partial melts fromeclogite may also contribute to less extreme alkalic OIB, asthese lavas have a number of compositional attributes, suchas high TiO2 and FeO* and low Al2O3, that have not been observedfrom partial melting of peridotite ± CO2. In upwellingmantle, formation of carbonatite and silicate melts from eclogiteand peridotite source lithologies occurs over a wide range ofdepths, producing significant opportunities for metasomatictransfer and implantation of melts. KEY WORDS: carbonated eclogite; experimental phase equilibria; partial melting; liquid immiscibility; ocean island basalts 相似文献
9.
Metamorphism of the Gile Mountain Formation and Waits River Formation in the Strafford Dome and Townshend-Brownington Syncline in east-central Vermont records two nappe-style events, D1 and D2, followed by doming. D1 formed a muscovite + biotite ± ilmenite schistosity subparallel to compositional layering, SO, and was followed by heating to garnet grade. The temperature and pressure at the end of D1 are estimated to be c . 450 C and 6-8 kbar. D2 variably crenulated and folded S1 during a nearly isothermal pressure increase of 1-2 kbar, calculated from compositions of garnet, which have inclusions trails with progressive crenulation and rotation of the S1 fabric. Similar P-T paths are computed for most of the area, suggesting that the later schistosity developed during emplacement of a regional nappe 3-6 km thick. There is a general lack of D3 (dome-stage) microstructures.
Near the Strafford-Willoughby Arch, staurolite and kyanite overgrew S2 in pelites, and plagioclase with increasing XAn overgrew S2 in calcic pelites, reflecting post-D2 heating to a maximum of 550-600 C. Metamorphic pressures at the end of D2 are fairly constant on the west side of the dome, indicating minor dome-stage uplift. In contrast, pressures at the thermal peak of metamorphism decrease by more than 4 kbar east of the dome. The observed pattern of isotherms and isobars is mainly the result of post-metamorphic, differential uplift and unroofing.
Finally, a minor, retrograde metamorphism produced the assemblage albite + epidote + K-feldspar + muscovite + chlorite, with grade increasing east toward the Connecticut River. 相似文献
Near the Strafford-Willoughby Arch, staurolite and kyanite overgrew S2 in pelites, and plagioclase with increasing X
Finally, a minor, retrograde metamorphism produced the assemblage albite + epidote + K-feldspar + muscovite + chlorite, with grade increasing east toward the Connecticut River. 相似文献
10.
Partial Melting Experiments of Peridotite + CO2 at 3 GPa and Genesis of Alkalic Ocean Island Basalts
We document compositions of minerals and melts from 3 GPa partialmelting experiments on two carbonate-bearing natural lherzolitebulk compositions (PERC: MixKLB-1 + 2·5 wt% CO2; PERC3:MixKLB-1 + 1 wt% CO2) and discuss the compositions of partialmelts in relation to the genesis of alkalic to highly alkalicocean island basalts (OIB). Near-solidus (PERC: 1075–1105°C;PERC3: 1050°C) carbonatitic partial melts with <10 wt%SiO2 and 40 wt% CO2 evolve continuously to carbonated silicatemelts with >25 wt% SiO2 and <25 wt% CO2 between 1325 and1350°C in the presence of residual olivine, orthopyroxene,clinopyroxene, and garnet. The first appearance of CO2-bearingsilicate melt at 3 GPa is 150°C cooler than the solidusof CO2-free peridotite. The compositions of carbonated silicatepartial melts between 1350 and 1600°C vary in the rangeof 28–46 wt% SiO2, 1·6–0·5 wt% TiO2,12–10 wt% FeO*, and 19–29 wt% MgO for PERC, and42–48 wt% SiO2, 1·9–0·5 wt% TiO2,10·5–8·4 wt% FeO*, and 15–26 wt% MgOfor PERC3. The CaO/Al2O3 weight ratio of silicate melts rangesfrom 2·7 to 1·1 for PERC and from 1·7 to1·0 for PERC3. The SiO2 contents of carbonated silicatemelts in equilibrium with residual peridotite diminish significantlywith increasing dissolved CO2 in the melt, whereas the CaO contentsincrease markedly. Equilibrium constants for Fe*–Mg exchangebetween carbonated silicate liquid and olivine span a rangesimilar to those for CO2-free liquids at 3 GPa, but diminishslightly with increasing dissolved CO2 in the melt. The carbonatedsilicate partial melts of PERC3 at <20% melting and partialmelts of PERC at 15–33% melting have SiO2 and Al2O3 contents,and CaO/Al2O3 values, similar to those of melilititic to basaniticalkali OIB, but compared with the natural lavas they are moreenriched in CaO and they lack the strong enrichments in TiO2characteristic of highly alkalic OIB. If a primitive mantlesource is assumed, the TiO2 contents of alkalic OIB, combinedwith bulk peridotite/melt partition coefficients of TiO2 determinedin this study and in volatile-free studies of peridotite partialmelting, can be used to estimate that melilitites, nephelinites,and basanites from oceanic islands are produced from 0–6%partial melting. The SiO2 and CaO contents of such small-degreepartial melts of peridotite with small amounts of total CO2can be estimated from the SiO2–CO2 and CaO–CO2 correlationsobserved in our higher-degree partial melting experiments. Thesesuggest that many compositional features of highly alkalic OIBmay be produced by 1–5% partial melting of a fertile peridotitesource with 0·1–0·25 wt% CO2. Owing to verydeep solidi of carbonated mantle lithologies, generation ofcarbonated silicate melts in OIB source regions probably happensby reaction between peridotite and/or eclogite and migratingcarbonatitic melts produced at greater depths. KEY WORDS: alkali basalts; carbonated peridotite; experimental petrology; ocean island basalts; partial melting 相似文献