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INTERNAL STRUCTURE AND MINERALOGY OF A ZONED ANORTHITE- AND GROSSULAR-BEARING LEUCOTONALITIC
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  • journal_title:The Canadian Mineralogist
  • Contributor:Milan Novák ; Petr Gadas
  • Publisher:Mineralogical Association of Canada
  • Date:2010-
  • Format:text/html
  • Language:en
  • Identifier:10.3749/canmin.48.3.629
  • journal_abbrev:Can Mineral
  • issn:0008-4476
  • volume:48
  • issue:3
  • firstpage:629
  • section:Articles
摘要

A zoned lenticular body of anorthite- and grossular-bearing leucotonalitic pegmatite, ~3–4 m thick and ~20–30 m long, cuts serpentinized lherzolite at Ruda nad Moravou, Staré Město Unit, Czech Republic. Its zoned internal structure consists of the following (sub)units from the contact inward: contact unit (Amp > Di), a highly heterogeneous transitional unit dominated by a leucocratic subunit (Pl > Qtz >> Di ~ Ep > Grs) with lesser proportions of grossular (Grs >> Qtz > Di) and diopside (Pl > Qtz ≈ Di) subunits, a coarse-grained unit (Pl > Qtz >> Grs ≈ Ep) with a graphic intergrowth of grossular + quartz, a graphic-blocky unit (Pl > Qtz > Kfs >> Grs), and a quartz core. White to grayish plagioclase An98–19 forms anhedral to euhedral grains, 0.1–2 mm to 10 cm in size. White to deep green K-feldspar occurs exclusively in the graphic-blocky unit. Colorless to pale brown grossular, varying from Grs98–100Adr0–1Prp0–1 (grossular subunit, quartz core) to Grs73–86 Adr11–24Sps1–2Prp0–1Sch0–4 (graphic intergrowths with Qtz), is present in all textural–paragenetic units in highly variable proportions. Subhedral to anhedral grains of pale to dark green diopside (XMg 97–82) ≤5 cm long occur almost exclusively in the contact unit and diopside subunit. Dark green grains of epidote-group minerals (epidote – clinozoisite – dissakisite – allanite), 0.1–20 mm in size, occur also in the outer units. Accessory minerals include common zircon as euhedral crystals of variable habits, ≤1 cm in size, locally associated with rare baddeleyite, U-rich zirconolite and gittinsite. Accessory titanite, fersmite, pyrochlore–betafite, apatite, monazite-(Ce), rutile, and biotite also were identified, along with several phases associated with subsolidus alteration: albite, clinozoisite, white mica, actinolite, Nb-rich titanite, Ba-rich feldspars, harmotome, chabazite-Ca, armenite, chlorite, prehnite, and pumpellyite-(Al). Plagioclase, diopside, and zircon show trends (decreasing Ca/Na, Mg/Fe, and Zr/Hf from outer to inner units) very similar to those expected of fractional crystallization. No simple compositional trends were recognized in grossular and epidote-group minerals except for decreasing ∑REE inward in the latter. Elevated contents of Mg and Cr in diopside and epidote-group minerals, limited exclusively to the contact unit and the diopside subunit, were controlled by contamination from the host serpentinite. Very low amounts of H2O-, F-, P-bearing minerals and an absence of micas strongly suggest low activities of H2O, F and P, whereas minerals containing CO2, B, Li and Be are absent. These findings imply a pegmatite-forming melt poor in H2O and other volatiles that crystallized sequentially inwardly from the contact with host rocks; crystallization likely proceeded during a single process. The mineral assemblages and chemical compositions of the minerals suggest a P > ~0.5–0.8 GPa and T > ~650–780°C of initial primary crystallization (liquidus conditions). The zonal internal structure, pegmatitic textures and fractionation trends in some minerals indicate rapid to moderate undercooling of the pegmatite-forming melt; low amounts of fluxes fit well with the boundary-layer model. The pegmatite from Ruda nad Moravou represents a new type of non-granitic pegmatite, leucotonalitic to quartz leucogabbroic in composition, significantly Ca-rich and with minor contamination by Mg.

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