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首页> 外文期刊>Contributions to Mineralogy and Petrology >Ankerite carbonatite from Swartbooisdrif, Namibia: the first evidence for magmatic ferrocarbonatite
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Ankerite carbonatite from Swartbooisdrif, Namibia: the first evidence for magmatic ferrocarbonatite

机译:纳米比亚Swartbooisdrif的方铁矿碳酸盐岩:岩浆性铁碳酸盐岩的第一个证据

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摘要

Although general accounts of carbonatites usually envisage Ca–Mg carbonate melts evolving by fractional crystallisation to Fe-rich residua, there is longstanding concern that ferrocarbonatites may actually be products of hydrothermal rather than magmatic processes. All previously published examples of ankerite- and/or siderite-carbonatites fail to show one or more of the isotopic criteria (all determined on the same sample) thought to be diagnostic of crystallised magmatic carbonate liquids. Ferrocarbonatite dykes cut Archaean-Proterozoic basement at Swartbooisdrif, adjacent to the NW Namibia-Angola border. Their age is uncertain but probably ~1,100 Ma and their associated fenites are rich in sodalite. Where unaffected by subsequent recrystallisation, their petrographic textures resemble those of silicate layered intrusions; ankerite, magnetite and occasionally calcite are cumulus phases, joined by trace amounts of intercumulus pyrochlore. Ankerite is zoned, from Ca(Mg, Fe2+)(CO3)2 cores towards ferroan dolomite rims. Calcite contains ~1.7% SrO, plus abundant, tiny exsolved strontianite grains. Magnetite is close to pure Fe3O4. Pyrochlore has fine-scale euhedral oscillatory zoning and light-REE-enriched rims. ICP-MS analysis of magnetite and pyrochlore from the carbonatite allows calculation of their modal amounts from mass-balance considerations. Sodalite from the fenite is REE poor. Geothermometry, using either the calcite-dolomite solvus or oxygen isotope fractionation between calcite and magnetite, gives temperatures in the range 420–460 °C. Initial Sr, Nd and Pb isotopic ratios of the ferrocarbonatites (87Sr/86Sr=0.7033; εNd=0.2–1.0; 206Pb/204Pb=16.37; 207Pb/204Pb=15.42; 208Pb/204Pb=36.01) are appropriate for an ~1,100-Ma magmatic carbonatite. Likewise, carbonate δ18O=8.0 and δ13C=–7.36 indicate little or no subsequent shift from magmatic values. It appears that dense ankerite and magnetite dominated crystal accumulation from a melt saturated in these phases, plus calcite and pyrochlore, with prior fractionation of a silicate mineral and apatite. The resulting ferrocarbonatite lacks a silicate mineral (excluding fenite xenocrysts) and apatite. It has unusually low (basalt-like) REE abundances and (La/Lu)n, and low concentrations of Ba, Rb, U, Th, Nb, Ta, Zr and Hf. Very high Nb/Ta and low Zr/Hf imply that the evolution of the parental magma involved immiscible separation of a carbonate from a silicate melt. The sodalite-dominated Swartbooisdrif fenites suggest that the parental melt also had a substantial Na content, in contrast with the ferrocarbonatite rock.
机译:尽管对碳酸盐岩的一般解释通常是设想Ca-Mg碳酸盐熔融物会通过分步结晶演变成富铁残渣,但长期以来人们一直担心,铁碳酸盐岩实际上可能是水热过程而不是岩浆作用过程的产物。以前发布的所有方铁矿和/或菱铁矿-碳酸盐实例均未显示出一种或多种同位素标准(均在同一样品上测定),这些标准可诊断出岩浆碳酸盐液体的结晶。碳酸盐岩大堤在西北纳米比亚-安哥拉边界附近的Swartbooisdrif切割了古生代元古代地下室。它们的年龄尚不确定,但可能约为1100 Ma,其相关的辉石富含方钠石。在不受后续重结晶影响的地方,它们的岩石学纹理类似于硅酸盐层状侵入体的岩石学纹理。方铁矿,磁铁矿和方解石为积云相,并伴有微量的积云烧绿石。钙铁矿从Ca(Mg,Fe2 + )(CO3 )2 岩心向铁白云岩边缘划分。方解石含有约1.7%的SrO,以及大量细小的溶解的锶锶矿颗粒。磁铁矿接近纯Fe3 O4 。烧绿石具有小规模的正反面振荡分区和富含轻稀土的轮辋。 ICP-MS分析磁铁矿中的磁铁矿和烧绿石,可以从质量平衡的角度计算出其模态量。来自菲涅石的方钠石稀土元素贫乏。使用方解石-白云石固溶体或方解石与磁铁矿之间的氧同位素分馏进行地热测定,温度范围为420–460°C。碳铁矿的初始Sr,Nd和Pb同位素比(87 Sr / 86 Sr = 0.7033;εNd= 0.2-1.0; 206 Pb / 204 Pb = 16.37; 207 Pb / 204 Pb = 15.42; 208 Pb / 204 Pb = 36.01)适用于约1,100-Ma岩浆碳酸盐岩。同样,碳酸盐δ18 O = 8.0和δ13 C = –7.36表示从岩浆值开始几乎没有或没有随后的偏移。看来,在这些相中饱和的熔体中,加上方解石和烧绿石,以及先有硅酸盐矿物和磷灰石的分馏,致密的铁矿石和磁铁矿主导了晶体的积累。所得的亚铁碳酸盐岩缺乏硅酸盐矿物(不包括亚铁酸盐异种晶)和磷灰石。它具有异常低的(类玄武岩)稀土元素丰度和(La / Lu)n ,以及低浓度的Ba,Rb,U,Th,Nb,Ta,Zr和Hf。 Nb / Ta极高而Zr / Hf极低意味着母岩浆的演化涉及碳酸盐与硅酸盐熔体的不混溶分离。以方钠石为主的Swartbooisdrif fenites表明,与亚铁碳酸盐岩相比,母体熔体也具有大量的Na含量。

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  • 来源
    《Contributions to Mineralogy and Petrology》 |2002年第3期|377-396|共20页
  • 作者单位

    Department of Geological Sciences University of Durham South Road Durham DH1 3LE UK;

    Department of Earth Sciences University of Cambridge Downing Street Cambridge CB2 3EQ UK;

    Department of Earth Sciences University of Cambridge Downing Street Cambridge CB2 3EQ UK;

    Department of Geology Royal Holloway University of London Egham Hill Egham Surrey TW20 OEX UK;

    Department of Geology McMaster University 1280 Main Street West Hamilton Ontario L8S 4M1 Canada;

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