ALBERT

Description: The Older Giant Dyke Complex is a differentiated alkaline intrusion of Proterozoic age (1154±16 Ma) and is the earliest of the late Gardar intrusions in the Tugtutôq-Ilímaussaq region. The dyke is approximately 20 km long by 0·5 km broad and comprises (i) marginal ‘border group’ rocks of alkali olivine gabbro, grading inwards to ferro-syenogabbro and (ii) an axial ‘central group’ of salic rocks ranging from augite syenite in the WSW to sodalite foyaite in the ENE.Chilled margins contain plagioclase (An53), olivine (Fo53), magnetite, ilmenite, and apatite as liquidus phases and later-crystallized augite (Di69Hd27Ac4) and biotite (Annite32). The coexisting Fe-Ti oxides indicate fO2 and T values just below the synthetic QFM buffer curve. In the border group, plagioclase cores zone into anorthoclase and soda-sanidine rims, olivines reach Fo16, pyroxenes Di32Hd59Ac9, and biotites Annite86. Interstitial pargasitic amphibole appears close to the innermost margins. In the central group, feldspars are all perthitic alkali feldspars and nepheline becomes a major, early crystallizing phase. Olivines range from Fo10-Fo4, in the augite-syenites where they coexist with ferro-salites Di50Hd47Ac3, but olivine is absent from foyaitic assemblages in which the pyroxenes range through aegirine-augite to pure aegirine. Interstitial amphiboles range from ferro-pargasite or hastingsite to katophorite and thence towards arfvedsonite, but are absent from the most differentiated rocks, whereas biotite occurs throughout the entire group in the range Annite71-Annite100.The parental magma, represented by the chilled margins, was a relatively anhydrous alkali olivine-basalt with an initial 87Sr/86Sr ratio of 0.70326. Its high Ti, P, Ba, and F contents are inferred to be features inherited from a primary magma, derived from the mantle as a small partial melt fraction which involved significant amounts of fluor-apatite and phlogopite. While all lithologies are considered as differentiates from this parental magma, there is both a well-defined field junction and a compositional hiatus between the border group and the central group rocks. Mineralogical considerations and REE patterns suggest that the later, more salic (?benmoreitic) magma from which the central group crystallized, related to the parental magma by ol-fsp-ap-FeTi oxide fractionation. Congelation in both border group and central group occurred by side-wall crystallization, but the salic magma became compositionally stratified, with upward concentration of alkalis and volatiles to produce a phonolitic upper facies which is preserved at the ENE end of the intrusion owing to subsequent axial tilting.

Description: SummaryCell dimensions have been measured from correctly indexed powder patterns of thirty natural and two synthetic orthopyroxenes. The natural specimens (mostly metamorphic) contain exsolved phases largely avoided during microprobe chemical analysis. Linear regression analysis between the cell dimensions and Mg, Al, Ca contents (ignoring minor elements) was quite unsatisfactory until a term in Mg2 was added. Two separate regression analyses for the ranges Mg 0–0·5 and 0·5–1 using only Mg, Al, and Ca were satisfactory. Olivine yielded satisfactory regressions for the whole range without a term in Mg2 (Louisnathan and Smith, 1968). The difference between olivine and pyroxene results from absence of site preference by Mg and Fe in olivine compared to strong preference in pyroxene revealed by electron density and Mössbauer studies (Bancroft, Burns, and Howie, 1967; Ghose and Hafner, 1967).The data were recalculated by means of a new best-fit procedure developed by Hey in which the errors in the chemical and physical parameters are considered simultaneously.Earlier measurements of a and b for plutonic pyroxenes are consistent within possible experimental uncertainties with those given here; however a and b data obtained by Kuno and by Hess on volcanic specimens are considerably higher by variable amounts. Although there are uncertainties in the Ca content and its effect on a and b, the larger dimensions probably result from lower site preference as indicated by Mössbauer studies.Prediction of Mg, Ca, and Al from just the cell dimensions is only moderately accurate even for metamorphic orthopyroxenes.

Description: Kûngnât Fjeld is an intrusive complex resulting from three intrusive events involving trachyte, mafic trachyte and hawaiite magmas tapped successively from a single magmatic source. In situ differentiation produced gabbroic, syeno-gabbroic, syenitic, and quartz syenitic cumulates showing strong cryptic variation. Layered sequences of syenitic rocks total c. 3500 m. The compositional range is extended by late-stage minor intrusions of microsyenite and peralkaline granite. The principal cumulus minerals are feldspar (Ab40An60 to Or45Ab51An4); olivine (Fo56 to Fo1) and clinopyroxene (Di70Hd27Ac3 to Di6Hd90Ac4 followed by an abrupt change of trend towards Di3Hd78Ac19 in the layered series and nearly pure aegirine in some peralkaline residues). Intercumulus phases are amphibole (hastingsite to ferro-edenite to ferro-actinolite in the layered series with riebeckite to arfvedsonite in some associated granites) and biotite (annite31 to annite98.5).