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西大别造山带红安高压榴辉岩主要矿物为石榴石、绿辉石、冻蓝闪石、石英和绿帘石,有时可见蓝闪石、多硅白云母和钠云母。石榴石具有生长环带且边缘成分变化大,可分为代表峰期的Ⅰ型边（XMg高、Grs低）和受退变质改造的Ⅱ型边（XMg低、Grs高）。石榴石内蓝闪石包体发育冻蓝闪石退变边,说明包体不能完全反映进变质条件。基质绿辉石比包体绿辉石Jd含量低,在一个晶体内成分有明显变化和沿解理缝发育冻蓝闪石,显示峰后绿辉石有成分变化和退变质改造。基质中冻蓝闪石晶体较大,核部见有蓝闪石残留,说明二者有成因联系。冻蓝闪石和绿辉石都发育后成合晶结构,石榴石有韭闪石的反应冠状体。在THERMOCALC程序计算的P-T视剖面图中,石榴石Ⅰ型边反映的峰期P-T条件为2.4~2.6GPa、570~585℃,和基质中多硅白云母Si含量等值线限定范围一致,对应硬柱石蓝闪石榴辉岩组合。石榴石Ⅱ型边P-T范围为1.9~2.4GPa、530~570℃,低于峰期条件。在可能的峰后降压过程中,岩石先后主要经历了硬柱石脱水生成绿帘石和蓝闪石、绿辉石退变为冻蓝闪石的反应阶段。绿辉石、冻蓝闪石发育的后成合晶说明晚期退变过程缺乏流体,石榴石的韭闪石冠状体也可能在该阶段产生,都受局部成分域控制。红安高压榴辉岩中各矿物与成分代表不同变质阶段,称其为冻蓝闪石榴辉岩只是对现有主要组成矿物的描述,不是基于共生关系的严格岩石学命名。 相似文献
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母乳中p,p’-DDE浓度是监测母体短期内p,p’-DDE的“静态”蓄积水平,估算婴幼儿每日摄入量的重要技术手段。本文旨在通过监测北京女性两个相邻哺乳期内母乳中p,p’-DDE浓度及变化,估算两次分娩间隔期母体内p,p’-DDE的“动态”富集速度,并根据每日摄入量掌握人体p,p’-DDE的长期变化趋势。在2009年至2019年期间,收集了43名女性首次分娩后六个月内和18名女性第二次分娩后六个月内的母乳样本,并采用气相色谱法检测了母乳中p,p’-DDE的浓度。实验结果表明,母乳中p,p’-DDE浓度在哺乳期持续下降。年龄和分娩次数是母乳中p,p’-DDE浓度的影响因素,p,p’-DDE浓度随母亲年龄增大而升高,随分娩次数增多而降低。18名母亲两个哺乳期内母乳中p,p’-DDE平均排泄速度计算结果表明,排泄速度从18.9μg/kg lipid/month降低到16.8μg/kg lipids/month。而母体两次分娩隔期内p,p’-DDE年富集速度估算值为正,分布在10.9~14.9μg/kg lipids/year之间,每日摄入量分布在29.8~40.8ng/day/kg.b.w.之间。因此北京女性哺乳期母体内p,p’-DDE月排泄速度与母体年富集速度数值相当,母体p,p’-DDE每日摄入量远低于世界卫生组织（WHO）建议值,北京女性是低风险暴露人群。 相似文献
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P-T-t轨迹作为变质岩的重要研究方法之一，对揭示岩石的构造演化过程具有重要意义。北大别饶拔寨镁铁-超镁铁岩形成的构造环境和就位过程长期以来尚存争议。本文通过岩相学观察、矿物化学研究和温压计计算，揭示出饶拔寨石榴辉石岩经历了四个变质演化阶段：1）超高压变质阶段（M1）：主要根据石榴子石中金红石的出溶，单斜辉石中石英的出溶和磷灰石中不透明矿物的出溶，结合前人研究，认为饶拔寨石榴辉石岩经历过超高压变质阶段（≥2.5GPa）；2）高压麻粒岩相阶段（M2）：矿物组合为石榴子石（变斑晶）和单斜辉石（基质）+斜长石（基质），记录的温压条件为T=648~700℃，P=1.47~1.94GPa；3）中压麻粒岩相阶段（M3）：以石榴子石外围发育的主要由斜方辉石+斜长石组成的内圈"白眼圈"为特征，形成的温压条件为T=781~796℃，P=0.92~0.98GPa；4）角闪岩相阶段（M4）：以石榴子石变斑晶周围发育的外圈"白眼圈"为特征，其矿物组合为角闪石+斜长石的后成合晶，形成的温压条件为T=663~685℃，P=0.50~0.58GPa。石榴辉石岩的锆石SIMS U-Pb定年得到了3组不同的交点年龄，分别为208.1~202.1Ma、227.6Ma和817.7Ma。根据锆石包裹体中角闪石+斜长石的组合，推断208.1~202.1Ma代表了角闪岩相变质年龄的下限，227.6Ma则是高压麻粒岩相的下限年龄，而新元古代年龄（817.7Ma）与区域上的变质岩原岩年龄一致，可能代表了其原岩年龄。结合前人研究，饶拔寨石榴辉石岩记录了顺时针的P-T-t轨迹，揭示了板片俯冲（超高压变质）-碰撞-折返（降压升温过程，~227Ma）-抬升（降压降温过程，208~202Ma）的完整过程。 相似文献
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佛子岭群位于大别造山带最北缘，处于华北和扬子两大板块结合部位，构造位置十分关键，是解析两大板块精细耦合过程和探究大别造山带晚古生代构造事件的重要单元。然而，由于长期以来佛子岭群一直被视为"浅变质"复理石沉积单元，因而对其变质演化过程的解析较为薄弱，制约了对大别造山带形成过程的全面理解。本次通过对老虎场-龚店地质剖面细致的观测，石榴黑云母片麻岩精细的岩相学、矿物化学分析、热力学评价和年代学研究，建立了佛子岭群一个逆时针P-T变质演化型式。研究显示，佛子岭群记录了Ⅰ、Ⅱ、Ⅲ和Ⅳ四个变质阶段，温压变化依次为：①T=658~663℃、P=1.08~1.16GPa→②T=755~762℃、P=1.21~1.45GPa→③T=549~554℃、P=1.08~1.19GPa→④P标定=0.3~0.6GPa、T=477~499℃，①至③为近等压升温和降温过程，③至④则表现为近等温降压型式。锆石U-Pb定年显示了1484±64Ma~1180±192Ma、995±35Ma~606±14Ma和370±14Ma~331±8Ma三组年龄，前两组代表了碎屑锆石年龄；第三组共计7颗锆石，年龄集中，Th/U比值0.01~0.03，加权平均年龄为344±11Ma，代表了主期变质年龄。结合此次地质剖面结构特征和岩石类型，以及前人白云母40Ar-39Ar的270~255Ma变质年龄，表明佛子岭群记录了两期变质事件，早期为晚古生代的拉张背景下的岛弧根部变质，晚期为晚古生代末的较为快速抬升构造热事件，并据此推测大别造山带可能为增生和碰撞复合型造山带。 相似文献
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绝大部分的亚硝酸盐和氰化物属于钙钛矿型结构,但有部分化合物为“反”钙钛矿型结构,充填空洞A位的阳离子的拓扑体积为0。阴离子团NO2-和CN-的拓扑体积都近乎常数,分别为41.73Å3和40.03Å3,标准方差σn-1=1.516和σn-1=1.25。由此,进一步证明了原来的一套离子拓扑体积数值的普适性。“反”钙钛矿型结构中A位阳离子的平均半径rA>1.00Å时,三价阳离子会产生扩容效应,其扩容系数大约是其本身拓扑体积的2倍;正钙钛矿型结构中,当A位是由半径较大的Cs+充填时,Cs+也会产生扩容效应,其扩容系数约为24Å3。氰化物中结晶水分子的拓扑体积近乎常数,为24Å3或0。 相似文献
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柴北缘锡铁山榴辉岩退变质成因角闪石40Ar/39Ar年代学研究 总被引：2，自引：2，他引：0
采用激光阶段加热40Ar/39Ar技术,对柴达木盆地北缘锡铁山榴辉岩退变质作用形成的榴闪岩和斜长角闪岩之角闪石进行了定年分析。09NQ44Amp来自榴闪岩,各阶段表观年龄(以现代空气氩40Ar/36Ar比值295.5扣除非放射性成因40Ar)构成了单调下降的阶梯状年龄谱。在反等时线图解上,2~4阶段数据点和5~18阶段数据点分别构成了两条等时线,等时年龄分别为427.6±10Ma和425.1±2.6Ma,对应的初始40Ar/36Ar比值则分别为435.2±6.1和705.3±13。角闪石09NQ43Amp来自榴辉岩强烈退变质作用形成的斜长角闪岩,40Ar/39Ar阶段加热分析也获得单调下降的年龄谱,在反等时线图解上其数据点3~6阶段和7~16阶段分别构成了两条等时线,等时年龄分别为418.9±2.9Ma和418.1±2.1Ma,对应的初始40Ar/36Ar比值则分别为493.7±2.8和685.8±34.3。等时线截距值高于现代大气40Ar/36Ar比值,表明角闪石中含过剩40Ar。同时,由低温和中-高温阶段加热数据点分别构成两条等时年龄基本一致,截距值却明显不同的等时线,表明在角闪石热力学性质不同的源区,存在两期明显不同且未混合的初始捕获Ar组分。等时年龄425~418Ma代表的是锡铁山榴辉岩角闪岩相退变质作用发生的时间。等时线图解法虽然有效的校正了角闪石中的过剩40Ar,但仅根据表观年龄图谱和等时线图谱还无法清晰判断过剩40Ar在角闪石中的赋存状态,有待进一步探讨。 相似文献
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古海水pH值代用指标——海洋碳酸盐硼同位素研究进展 总被引：1，自引：0，他引：1
仪器测量的海水pH记录太短，无法评估海水pH自然变化的频率和幅度,并预测未来大气CO2急剧增加后海水酸度的响应。海相碳酸盐的硼同位素是目前恢复古海洋pH的有效途径，倍受古气候—环境学家的重视。评述了近年来海洋碳酸盐的硼同位素的最新研究成果和研究现状，重点探讨了海相碳酸盐的硼同位素的测定方法、硼同位素—pH模型和古海水pH恢复等前沿内容，旨在提供一个系统的海洋碳酸盐硼同位素—pH系统的基本概念及研究思路，以利于气候学、地质学界了解这一交叉领域的发展动态。 相似文献
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对2004年获取的天山奎屯河哈希勒根51号冰川1个雪坑和哈密庙尔沟平顶冰川4个雪坑的离子浓度特征进行了研究,结果表明：Ca2+、NO-3和SO42-是哈密庙尔沟平顶冰川雪坑雪层和积累区雪坑底部冰中的主要离子（尤其是Ca2+ ）,其雪层中的主要阳离子关系可在底部冰中得以较好的反映,但雪层中各离子浓度与海拔的相关性不明显,可能与海拔的跨度较小和挖取的雪坑较疏有关;雪坑底部冰中的离子浓度与海拔间明显的相关性说明淋融作用随着海拔升高、气温降低而逐渐减弱。SO42-和Ca2+是奎屯河哈希勒根51号冰川雪坑中的主要离子（尤其是SO42-）,其雪坑离子化学特征与哈密庙尔沟平顶冰川差别较大,可能与哈密庙尔沟平顶冰川处于塔克拉玛干沙漠、古尔班通古特沙漠和鄯善沙漠的下风向相关,还可能与雪层内淋融作用的强弱和沉积通量的高程效应有关。哈密庙尔沟平顶冰川积累区雪坑中NH4+、NO3-和K+的Cs/Ci较Ca2+、Mg2+和Na+要大,奎屯河哈希勒根51号冰川Na+和NH4+的“雪冰比”较Cl-、SO42-、Mg2+和Ca2+要大,说明这两条冰川雪坑中的Ca2+和Mg2+信号较其它离子可能更易于在冰芯记录中保存下来,为冰芯研究和古气候记录的恢复提供了保障。 相似文献
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贵阳地表水-地下水的硫和氯同位素组成特征及其污染物示踪意义 总被引：5，自引：0，他引：5
喀斯特地表水和地下水的交换活跃,地下水系统容易受到地表污染物的污染。为了解喀斯特城市地表水—地下水系统污染特征和污染物质来源,对贵阳市地表水、地下水、雨水和城市排污污水的硫同位素和氯同位素组成变化进行了研究。贵阳市不同类型水体的δ37Cl值在-4.07‰～+2.03‰之间变化,δ34SSO4值变化为-20.4‰～+20.9‰。大气输入物质和城市排污污水的δ37Cl、δ34S及Cl-/SO42-比值与地表水和地下水的不同,稳定硫和氯同位素的结合研究为示踪地下水污染物来源提供了有效研究手段。贵阳市地下水中的Cl-和SO42-至少有4种来源,人为活动通过城市排污和大气输入向地下水系统大量输入了硫酸盐和氯离子。 相似文献
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HARLOV DANIEL E.; JOHANSSON LEIF; VAN DEN KERKHOF ALFONS; FORSTER HANS-JURGEN 《Journal of Petrology》2006,47(1):3-33
A localized dehydration zone, Söndrum stone quarry, Halmstad,SW Sweden, consists of a central, 1 m wide granitic pegmatoiddyke, on either side of which extends a 2·5–3 mwide dehydration zone (650–700°C; 800 MPa; orthopyroxene–clinopyroxene–biotite–amphibole–garnet)overprinting a local migmatized granitic gneiss (amphibole–biotite–garnet).Whole-rock chemistry indicates that dehydration of the graniticgneiss was predominantly isochemical. Exceptions include [Y+ heavy rare earth elements (HREE)], Ba, Sr, and F, which aremarkedly depleted throughout the dehydration zone. Systematictrends in the silicate and fluorapatite mineral chemistry acrossthe dehydration zone include depletion in Fe, (Y + HREE), Na,K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusionchemistry is similar in all three zones and indicates the presenceof a fluid containing CO2, NaCl, and H2O components. Water activitiesin the dehydration zone average 0·36, or XH2O = 0·25.All lines of evidence suggest that the formation of the dehydrationzone was due to advective transport of a CO2-rich fluid witha minor NaCl brine component originating from a tectonic fracture.Fluid infiltration resulted in the localized partial breakdownof biotite and amphiboles to pyroxenes releasing Ti and Ca,which were partitioned into the remaining biotite and amphibole,as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, andF. At some later stage, H2O-rich fluids (H2O activity >0·8)gave rise to localized partial melting and the probable injectionof a granitic melt into the tectonic fracture, which resultedin the biotite and amphibole recording a diffusion profile forF across the dehydration zone into the granitic gneiss as wellas a diffusion profile in Fe, Mn, and Mg for all Fe–Mgsilicate minerals within 100 cm of the pegmatoid dyke. KEY WORDS: charnockite; fluids; CO2; brines; localized dehydration; Söndrum 相似文献
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An understanding of the Okcheon Metamorphic Belt (OMB) in South Korea is central to unraveling the tectono-metamorphic evolution of East Asia. Amphibole-bearing rocks in the OMB occur as calcsilicate layers and lenses in psammitic rocks, in the psammitic rocks themselves, and in the mafic volcanic layers and intrusives. Most amphiboles fail to show 40Ar/39Ar plateau ages; those that do have ages ranging from 132 to 975 Ma. The disturbed age pattern and wide variation in 40Ar/39Ar ages can be related to metamorphic grade, retrograde chemical reactions, excess Ar and amphibole composition. The oldest age (975 Ma) can be interpreted either as an old igneous or metamorphic age predating sedimentation or a false age caused by excess Ar. The youngest age of 132 Ma and the disturbed age pattern found in amphiboles from rocks located close to Jurassic granitoids are the result of retrograde thermal metamorphic effects accompanying intrusion of the granitoids. Some medium- or coarse-grained amphiboles in the calcsilicates are aggregates of fine-grained crystals. As a result, they are heterogeneous and prove to be readily affected by excess Ar. A disturbed age pattern in amphiboles from the calcsilicates occurring in the high-grade metamorphic zone may also be the product of excess Ar. On the other hand, the disturbed pattern of amphiboles present in the calcsilicates from the low-grade metamorphic zone could arise from both excess Ar and mixed ages. However, amphiboles from psammitic rocks and some calcsilicates in the high-grade metamorphic zone and in intrusive metabasites display real plateau ages of 237 to 261 Ma. The temperature conditions in the high-grade metamorphic zone were higher than the argon closing temperature for amphibole, and the amphiboles in this zone give plateau ages only when they are homogeneous in composition, lack excess Ar, and have not been thermally affected by intrusion of the granitoids. The unmodified 40Ar/39Ar ages prove rather younger than the age of the Late Paleozoic metamorphic event of 280 to 300 Ma, but they are close to muscovite K-Ar ages of 263 to 277 Ma. These 40Ar/39Ar amphibole ages are interpreted as the time of cooling that followed the main regional, intermediate-P/T metamorphic climax. The results demonstrate that interpretation of 40Ar/39Ar amphibole ages in an area subjected to several metamorphic events can be accomplished only by undertaking a thorough tectono-metamorphic study, accompanied by detailed chemical analysis of the amphiboles. 相似文献
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Four pairs of associated calcic and sodic amphiboles from blueschistfacies metamorphic rocks were analyzed with the electron microprobeand studied by single-crystal X-ray diffraction techniques.Except for ranges in the ratios Mg/(Mg+Fe) and Fe3+/(Fe3++Al+Ti),the sodic amphiboles are similar in chemical composition. Theamount of calcium in the M(4)-site ranges only from 0·18to 0·21 ion per formula unit. The calcic amphiboles,in addition to a range in Mg/(Mg+Fe), vary in Na/(Na+Ca) ratio(0·29–0·48). Three of the calcic amphibolescontain less than 1·5 calcium ions per formula unit,indicating a significant solid solution of sodic amphibole componentsin the calcic amphibole phase. The a and b unit-cell parametersof the calcic amphiboles decrease with increased content ofthe sodic component. 相似文献
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Chemical analyses for the following amphibole pairs are presented:anthophyllite—tremolite (or actinolite, or hornblende),cummingtonite (or grunerite)–actinolite (or hornblende),cummingtonite (or grunerite)–anthophyllite (or gedrite),and manganoan cummingtonitemagnesioriebeckite. Nineteen analyses of such pairs are quoted from the literature,and thirty-seven additional pairs have been newly analyzed byelectron probe techniques. Quantitative microprobe determinationsof Si, Al, Fe, Mn, Mg, Ca, and Na were made on polished thin-sections,using naturally occurring, analyzed, homogeneous amphibolesas standards. The literature analyses and the electron probeanalyses for metamorphic, two-amphibole assemblages are givenfor amphiboles in physical contact, which show no textural evidenceof one amphibole being a reaction or alteration product of theother. The chemical data for some of the volcanic, two—amphiboleassemblages were obtained from occurrences that probably donot represent equilibrium pairs. The chemical data are used to determine the extent of the miscibilitygaps between the various amphibole series and the fractionationof the major elements between the two amphiboles of a pair.Anthophyllite and members of the cummingtonite-grunerite seriesgenerally have a larger Fe(total)/Mg ratio than the coexistingcalcic amphibole. The maximum CaO, Al2O3and Na2O contents ofcummingtonite in metamorphic cummingtonite—hornblendepairs are 19 and 32, 02 weight per cent, respectively. Themaximum CaO, A12O3, and Na2O contents of cummingtonite in metamorphiccummingtonite-hornblende pairs are 19, 32, and 02 weightper cent, respectively. Larger CaO and Al2O3 values reportedin the literature were found to be too high because of admixtureof actinolite or hornblende in the analyzed separates. Smallamounts of MnO tend to concentrate preferentially in anthophylliteor cummingtonite of anthophyllite-hornblende and cummingtonite-hornblendepairs. Anthophyllite-cummingtonite pairs may show very similarFe(total)/Mg ratios and differ slightly in Al2O3 content only. 相似文献
17.
MOINE B. N.; GREGOIRE M.; O'REILLY S. Y.; SHEPPARD S. M. F.; COTTIN J. Y. 《Journal of Petrology》2001,42(11):2145-2167
A basanite dyke in the Kerguelen Archipelago contains abundantcomposite mantle xenoliths consisting of spinel-bearing dunitescross-cut by amphibole-rich veins. Two types of veins (thickand thin) have been distinguished: the thick veins representalmost complete crystallization products of highly alkalinemelts similar to the host basanites, whereas thin veins areprecipitates from fractionates of the parental melts to thethick veins. These fractionated fluids are enriched in H2O relativeto the parental melts. The amphiboles in the thin veins arelower in Ti and higher in Nb, Ta, Zr and Hf than amphibolesin the thick veins. This fractionation of high field strengthelements (HFSE) is consistent with a combination of the changingcomposition of the fractionated fluids and the change in intrinsicamphibole–fluid partition coefficients for HFSE in fluidswith higher aH2O and lower aTiO2. The trace element contentof amphiboles disseminated in dunitic wall-rocks is closelyrelated to the composition of adjacent veins and thus theseamphiboles are precipitates from fluids percolating into thedunite from the veins. Disseminated amphibole reflects the compositionof the percolating melt, which is similar to that of the associatedveins. KEY WORDS: mantle amphibole; Kerguelen; HFSE fractionation; mantle HFSE; mantle xenoliths 相似文献
18.
Calculated Phase Relations in the System Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O with Applications to UHP Eclogites and Whiteschists 总被引：2，自引：0，他引：2
Pressure–temperature grids in the system Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O and its subsystems have been calculatedin the range 15–45 kbar and 550–900°C, usingan internally consistent thermodynamic dataset and new thermodynamicmodels for amphibole, white mica, and clinopyroxene, with thesoftware THERMOCALC. Minerals considered for the grids includegarnet, omphacite, diopside, jadeite, hornblende, actinolite,glaucophane, zoisite, lawsonite, kyanite, coesite, quartz, talc,muscovite, paragonite, biotite, chlorite, and plagioclase. Compatibilitydiagrams are used to illustrate the phase relationships in thegrids. Coesite-bearing eclogites and a whiteschist from Chinaare used to demonstrate the ability of pseudosections to modelphase relationships in natural ultrahigh-pressure metamorphicrocks. Under water-saturated conditions, chlorite-bearing assemblagesin Mg- and Al-rich eclogites are stable at lower temperaturesthan in Fe-rich eclogites. The relative temperature stabilityof the three amphiboles is hornblende > actinolite > glaucophane(amphibole names used sensu lato). Talc-bearing assemblagesare stable only at low temperature and high pressure in Mg-and Al-rich eclogites. For most eclogite compositions, talccoexists with lawsonite, but not zoisite, in the stability fieldof coesite. Water content contouring of pressure–temperaturepseudosections, along with appropriate geotherms, provides newconstraints concerning dehydration of such rocks in subductingslabs. Chlorite and lawsonite are two important H2O-carriersin subducting slabs. Depending on bulk composition and pressure–temperaturepath, amphibole may or may not be a major H2O-carrier to depth.In most cases, dehydration to make ultrahigh-pressure eclogitestakes place gradually, with H2O content controlled by divariantor higher variance assemblages. Therefore, fluid fluxes in subductionzones are likely to be continuous, with the rate of dehydrationchanging with changing pressure and temperature. Further, eclogitesof different bulk compositions dehydrate differently. Dehydrationof Fe-rich eclogite is nearly complete at relatively shallowdepth, whereas Mg- and Al-rich eclogites dehydrate continuouslydown to greater depth. KEY WORDS: dehydration; eclogites; phase relations; THERMOCALC; UHP metamorphism; whiteschists 相似文献
19.
Chromium as Cr3+ substitutes for octahedrally coordinated Alin upper-mantle minerals, thereby reducing the activity of Al2O3in the system and hence the concentration of Al2O3 in partialmelts. The effect of Cr2O3 on melt compositions multiply saturatedwith the spinel lherzolite phase assemblage has been quantifiedin the system CaO–MgO–Al2O3–SiO2–Cr2O3at 1·1 GPa as a function of 100 Cr/(Cr + Al) in the spinel(Cr#sp). The decrease of Al2O3 in the melt with increasing Cr#spis accompanied by increasing MgO and SiO2, whereas CaO remainsalmost constant. Consequently, the CaO/Al2O3 ratio of the meltincreases with Cr#sp, and the melt becomes richer in normativediopside, hypersthene and quartz. The effect may explain certainmantle melts with unusually high CaO/Al2O3 ratios. The concentrationof Cr2O3 in the melt remains low even at high Cr#sp, which meansthat the strong effect of Cr2O3 on partial melting equilibriais not readily apparent from its concentration in the melt itself.The existence of a highly refractory major component such asCr2O3 nullifies simplified conclusions from the ‘inverseapproach’ in the experimental study of basalt petrogenesis,as there is insufficient information in the composition of thepartial melt to reconstruct the conditions of melting. KEY WORDS: basalt petrogenesis; partial melting; reversal experiment; spinel lherzolite; system CMAS–Cr2O3; CaO/Al2O3 of melt; effect of Cr2O3 相似文献
20.
The following article presents constraints of the stability of Mg-rich (Mg/(Mg + Fe2+) > 0.5) calcic amphibole in both calc-alkaline and alkaline magmas, testing of previous thermobarometers, and formulation
of new empirical equations that take into consideration a large amount of literature data (e.g. more than one thousand amphibole
compositions among experimental and natural crystals). Particular care has been taken in choosing a large number of natural
amphiboles and selecting quality experimental data from literature. The final database of experimental data, composed of 61
amphiboles synthesized in the ranges of 800–1,130°C and 130–2,200 MPa, indicates that amphibole crystallization occurs in
a horn-like P–T stability field limited by two increasing curves (i.e. the thermal stability and an upper limit), which should start to bend
back to higher pressures. Among calcic amphiboles, magnesiohornblendes and tschermakitic pargasites are only found in equilibrium
with calc-alkaline melts and crystallize at relatively shallow conditions (P up to ~1 GPa). Kaersutite and pargasite are species almost exclusively found in alkaline igneous products, while magnesiohastingsite
is equally distributed in calc-alkaline and alkaline rocks. The reliability of previous amphibole applications was checked
using the selected experimental database. The results of this testing indicate that none of the previous thermobarometers
can be successfully used to estimate the P, T and fO2 in a wide range of amphibole crystallization conditions. Multivariate least-square analyses of experimental amphibole compositions
and physico-chemical parameters allowed us to achieve a new thermobarometric model that gives reasonably low uncertainties
(T ± 23.5°C, P ± 11.5%, H2Omelt ± 0.78wt%) for calc-alkaline and alkaline magmas in a wide range of P–T conditions (up to 1,130°C and 2,200 MPa) and ∆NNO values (±0.37 log units) up to 500 MPa. The AK-[4]Al relation in amphibole can be readily used to distinguish crystals of calc-alkaline liquids from those of alkaline magmas.
In addition, several chemometric equations allowing to estimate the anhydrous composition of the melts in equilibrium with
amphiboles of calc-alkaline magmas were derived. 相似文献