Magma dynamics at the base of an evolving mafic magma chamber: Incompatible element evidence from the Partridge River intrusion, Duluth Complex, Minnesota, USA

A characteristic feature of the Partridge River intrusion of the Keweenawan Duluth Complex is the approximately fivefold to ninefold increase in the concentrations of incompatible elements in the lower zone compared with cumulates stratigraphically higher. The concentrations of incompatible elements decrease from the lower zone upward to steady state values, which is ascribed to variations in the proportions of trapped liquid rather than variable degrees of fractional crystallization of a single parental magma. The calculated average composition of trapped liquid using our algorithm is similar to typical Keweenawan low-alumina, high Ti---P basalts associated with the Duluth Complex but is different from the leading edge ferrodioritic liquid quenched in the chilled margin of the intrusion. This difference suggests that the chilled margin does not represent the original (parental) magma composition from which the whole intrusion solidified, and that the enrichment of incompatible elements may be related to the local flotation of magmatic suspensions. To test the latter hypothesis numerically, we have used heat-mass transfer models, assuming a sheet-like magma chamber, to calculate the parameters of the model that best reproduce the observed distribution of incompatible elements in a mush zone at the base of the Partridge River intrusion. The results indicate that a mush zone enriched in the incompatible elements is produced if the velocity of movement of the lower solidification front into the magma body was less than the floating velocity of the bulk crystal mush. The dynamic parameters that best reproduce the observed distribution of incompatible elements include a magma emplacement pressure of 2 kbar, critical crystallinities of 50–68% in the mush zone from which the liquid is being expelled, and an emplacement temperature of 1160°C for the initial magma.     

Petrology of middle proterozoic diabases and picrites from Lake Nipigon,Canada

Mafic rocks at Lake Nipigon provide a record of rift-related continental basaltic magmatism during the Keweenawan event at 1109 Ma. The mafic rocks consist of an early, volumetrically minor suite of picritic intrusions varying in composition from olivine gabbro to peridotite and a later suite of tholeiitic diabase dikes, sheets and sills. The diabase occurs primarily as two 150 to 200 m thick sills with a textural stratigraphy indicating that the sills represent single cooling units. Compositional variation in the sills indicates that they crystallized from several magma pulses.The diabases are similar in chemistry to olivine tholeiite flood basalts of the adjacent Keweenawan rift, particularly with respect to low TiO₂, K₂O and P₂O₅. The picrites have higher TiO₂, K₂O and P₂O₅ than the diabases and are similar to, but more primitive than, high Fe-Ti basalts which erupted early in the Keweenawan volcanic sequence.All of the rocks crystallized from fractionated liquids. The picrites are cumulate rocks derived at shallow crustal depths from a magma controlled predominantly by olivine fractionation. Picritic chills are in equilibrium with olivine phenocrysts of composition Fo₈₀ and are interpreted to represent the least evolved liquids observed. The parental magma of the picrites was probably Fe rich relative to the parental magma of the diabase. The diabase sills crystallized from an evolved basaltic liquid controlled by cotectic crystallization of plagioclase and lesser olivine and pyroxene.The emplacement of dense olivine phyric picritic magmas early in the sequence, followed by later voluminous compositionally evolved magmas of lower density suggests the development of a crustal density filter effect as the igneous event reached a peak. Delamination of the crust-mantle interface may have resulted in the transition from olivine controlled primitive magma to fractionated magma through the development of crustal underplating.     

新疆东天山黄山东岩体橄榄石成因意义探讨

黄山东岩体位于新疆东天山造山带中段,由四次岩浆侵入形成:第一次侵入形成了岩体上部的橄榄辉长岩、角闪辉长岩和闪长岩,构成岩体的主体;第二次侵入形成辉长苏长岩,呈岩墙状分布于岩体西端和西北部;第三次侵入岩石为斜长二辉橄榄岩,位于岩体下部,为主要的赋矿岩石;第四次侵入岩石为底部角闪辉长岩。橄榄石为第三次侵入的斜长二辉橄榄岩和第一次侵入的橄榄辉长岩主要造岩矿物之一,橄榄石的镁橄榄石牌号(Fo)值介于68.5～82.5之间。其中含硫化物斜长二辉橄榄岩中的橄榄石具有较高的Fo值(79.7～82.5);斜长二辉橄榄岩中橄榄石的Fo值为78.3～79.9;而基性程度较低的橄榄辉长岩中橄榄石具有较低的Fo值(68.5～72.2)。利用橄榄石矿物成分计算得出黄山东岩体母岩浆Mg#(Mg2+/(Mg2++Fe2+))为0.59,为原生玄武质岩浆经历结晶分异作用形成。模拟计算结果显示黄山东岩体不含矿岩石中橄榄石是母岩浆经过2%的橄榄石结晶分异且硫达到饱和后,在硫化物熔离的同时岩浆发生橄榄石结晶而形成,并且橄榄石︰硫化物≈50︰1,部分橄榄石成分投点在橄榄石结晶和硫化物熔离的模拟曲线右下侧,指示它们可能受到晶间硅酸盐熔浆作用的影响。含硫化物斜长二辉橄榄岩中Fo值与Ni含量呈负相关关系,说明橄榄石与硫化物熔体之间发生了Fe-Ni交换反应。     

Anorthositic Rocks of the Duluth Complex: Examples of Rocks Formed from Plagioclase Crystal Mush

Anorthositic rocks compose 35–40% of the Middle Proterozoic(Keweenawan; 1?1 Ga) Duluth Complex—a large, compositemafic body in northeastern Minnesota that was intruded beneatha comagmatic volcanic edifice during the formation of the Midcontinentrift system. Anorthositic rocks, of which six general lithologictypes occur in one area of the complex, are common in an earlyseries of intrusions. They are characterized on a local scale(meters to kilometers) by nonstratiform distribution of rocktypes, variably oriented plagioclase lamination, and compositeintrusive relationships. Variably zoned, subhedral plagioclaseof nearly constant average An (60) makes up 82–98% ofthe anorthositic rocks. Other phases include granular to poikiliticolivine (Fo_66–38), poikilitic clinopyrox-ene (En'_73–37),subpoikilitic Fe-Ti oxides, and various late-stage and secondaryminerals. Whole-rock compositions of anorthositic rocks are modelled bymass balance to consist of three components: cumulus plagioclase(70–95 wt.%), minor cumulus olivine (0–5%), anda gabbroic postcumulus assemblage (5–27%) representinga trapped liquid. The postcumulus assemblage has textural andcompositional characteristics which are consistent with crystallizationfrom basaltic magma ranging from moderately evolved olivinetholeiite to highly evolved tholeiite (mg=60–25). Sympatheticvariations of mg in plagioclase and in mafic minerals suggestthat cumulus plagioclase, though constant in An, was in approximateequilibrium with the variety of basaltic magma compositionswhich produced the postcumulus assemblages. Standard models of mafic cumulate formation by fractional crystallizationof basaltic magmas in Duluth Complex chambers, although ableto explain the petrogenesis of younger stratiform troctoliticto gabbroic intrusions, are inadequate to account for the field,petrographic, and geochemical characteristics of the anorthositicrocks. Rather, we suggest an origin by multiple intrusions ofplagioclase crystal mushes—basaltic magmas charged withas much as 60% intratelluric plagioclase. The high concentrationsof cumulus plagioclase (70–95%) estimated to compose theanorthositic rocks may reflect expulsion of some of the transportingmagma during emplacement or early postcumulus crystallizationof only plagioclase from evolved hyperfeldspathic magma. Althoughthe evolved compositions of anorthositic rocks require significantfractionation of mafic minerals, geophysical evidence indicatesthat ultramafic rocks are, as exposure implies, rare in theDuluth Complex and implies that plagioclase crystal mushes werederived from deeper staging chambers. This is consistent withinterpretations of olivine habit and plagioclase zoning. Moreover,plagioclase could have been segregated from coprecipitatingmafic phases in such lower crustal chambers because of the buoyancyof plagioclase in basaltic magmas at high pressure. The geochemicaleffects of plagioclase suspension in basaltic magmas are consistentwith observed compositions of cumulus plagioclase in the anorthositicrocks and with the geochemical characteristics of many comagmaticbasalts. The petrogenesis of the anorthositic rocks and theoverall evolution of Keweenawan magmas can be related to thedynamics of intracontinental rift formation.     

Geochemical and mineralogical evidence for the occurrence of at least three distinct magma types in the ‘famous’ region

Bulk rock major and trace element variations in selected basalts from the Famous area, in conjunction with a detailed study of the chemical compositions of phenocryst minerals and associated melt inclusions are used to place constraints on the genetic relationship among the various lava types. The distribution of NiO in olivine and Cr-spinel phenocrysts distinguishes the picritic basalts, plagioclase phyric basalts and plagioclase-pyroxene basalts from the olivine basalts. For a given Mg/Mg+Fe²⁺ atomic ratio of the mineral, the NiO content of these phenocrysts in the former three basalt types is low relative to that in the phenocrysts in the olivine basalts. The Zr/Nb ratio of the lavas similarly distinguishes the olivine basalts from the plagioclase phyric and plagioclase pyroxene basalts and, in addition, distinguishes the picritic basalts from the other basalt types. These differences indicate that the different magma groups could not have been processed through the same magma chamber, and preclude any direct inter-relationship via open or closed system fractional crystallization.The Fe-Mg partitioning between olivine and host rock suggests that the picritic basalts represent olivine (±Cr-spinel) enriched magmas, derived from a less MgO rich parental magma. The partitioning of Fe and Mg between olivine, Cr-spinel and coexisting liquid is used to predict a primary magma composition parental to the picritic basalts. This magma is characterized by relatively high MgO (12.3%) and CaO (12.6%) and low FeO^* (7.96%) and TiO₂ (0.63%).Least squares calculations indicate that the plagioclase phyric basalts are related to the plagioclase-pyroxene basalts by plagioclase and minor clinopyroxene and olivine accumulation. The compositional variations within the olivine basalts can be accounted for by fractionation of plagioclase, clinopyroxene and olivine in an open system, steady state, magma chamber in the average proportions 453223. It is suggested that the most primitive olivine basalts can be derived from a pristine mantle composition by approximately 17% equilibrium partial melting. Although distinguished by its higher Zr/Nb ratio and lower NiO content of phenocryst phases, the magma parental to the picritic basalts can be derived from a similar source composition by approximately 27% equilibrium partial melting. It is suggested that the parental magma to the plagioclase-pyroxene and plagioclase phyric basalts might have been derived from greater depth resulting in the fractionation of the Zr/Nb ratio by equilibration with residual garnet.C.O.B. Contribution No. 722     

Boninite primary magmas: Evidence from the Cape Vogel Peninsula,PNG

Boninites from Cape Vogel, PNG, are dominantly pyroxene-glass rocks, but many contain olivine, sometimes as refractory as Fo₉₄. We derive a parental magma for this suite (in equilibrium with Fo₉₄) which contains 20 wt.% MgO and is quartz-normative. This liquid is hydrous, and from petrographie evidence and whole rock H₂O⁺ values, we estimate it to contain 2–3 wt.% H₂O. These data suggest olivine fractionation and primary magmatic water are important in boninite genesis, but both are often obscured by later alteration. The derived parental magma has probably formed at 1,250–1,300° C and low pressures (< ?10kB) and is similar to those which gave rise to olivine-clinoenstatite phyric boninites from New Caledonia and from Howqua, Australia, and possibly to a proposed parental magma for the Bushveld Complex.     

Simulation of the geochemical structure of the Ioko-Dovyren layered intrusion,northwestern Baikal area

The processes of differentiation in the magmatic chamber of the Ioko-Dovyren layered dunite-troctolite-gabbro-gabbronorite massif were simulated using the COMAGMAT-3.5 software package, which is based on the convection-accumulation model for the crystallization of magmatic intrusions. The initial magma composition was assumed to be equal to the weighted mean composition of the rocks composing the intrusion (wt %: 43.92 SiO₂, 9.72 Al₂O₃, 10.53 FeO, 27.88 MgO, 6.99 CaO, 0.59 Na₂O, 0.07 K₂O, and 0.11 TiO₂). The results obtained by simulating the crystallization of this composition within a pressure range of 0–10 kbar indicate that the crystallization sequence determined for the rocks Ol + Chr → Ol+ Pl+ Chr → Ol + Pl+ CPx → ± Ol + Pl+ CPx + LowCaPx in an anhydrous system takes place under pressures of 0–2 kbar. A series of simulations for a system closed with respect to oxygen yielded estimates for the phase and chemical composition of the emplaced magma and the parameters of the optimum model, which reproduces accurately enough the geochemical structure of the Ioko-Dovyren intrusion: the naturally occurring distributions of minerals and components in its vertical section. The correlation coefficients between the concentrations of oxides determined in the rocks and calculated within the model are \(r_{MgO,Al_2 O_3 ,CaO} \) ≥ 0.9 and \(r_{FeO,SiO_2 ,Na_2 O} \) ≥ 0.6. The simulated phase composition of the magma during its emplacement corresponded to melt + olivine (Fo ₈₉). The crystallinity of the parental magma was determined to have been equal to approximately 40 vol % at an assumed cumulus density of 90% near the lower contact and 70% near the upper one. The temperature of the magma during its emplacement was close to 1340°C at a pressure of 1 kbar. In the model, plagioclase and clinopyroxene appear on the liquidus at T?1255°C at T?1210°C, respectively, and the crystallization sequence of cumulus minerals corresponds to that observed in nature. The liquid phase (melt) of the parental magma during its emplacement had the following composition (wt %): 45.95 SiO₂, 15.93 Al₂ O₃, 14.49 MgO, 10.88 FeO, 11.46 CaO, 0.97 Na₂O, 0.11 K₂O, and 0.18 TiO₂. Our results confirm the plausibility of the hypothesis that the inner structure of the Ioko-Dovyren intrusion was formed by the emplacement and differentiation of a single magma portion with no less than 40 vol % crystallinity.     

Melting and phase relations in the plane tholeiite-lherzolite-nepheline basanite to 40 kilobars with geological implications

Six crystalline mixtures, picrite, olivine-rich tholeiite, nepheline basanite, alkali picrite, olivine-rich basanite, and olivine-rich alkali basalt were recrystallized at pressures to 40 kb, and the phase equilibria and sequences of phases in natural basaltic and peridotitic rocks were investigated.The picrite was recrystallized along the solidus to the assemblages (1) olivine+orthopyroxene+ clinopyroxene +plagioclase+spinel below 13 kb, (2) olivine+orthopyroxene+clinopyroxene+spinel between 13 kb and 18 kb, (3) olivine+orthopyroxene+clinopyroxene+ garnet+spinel between 18 kb and 26 kb, and (4) olivine+clinopyroxene+garnet above 26 kb. The solidus temperature at 1 atm is slightly below 1,100° and rises to 1,320° at 20 kb and 1,570° at 40 kb. Olivine is the primary phase crystallizing from the melt at all pressures to 40 kb.The olivine-rich tholeiite was recrystallized along the solidus into the assemblages (1) olivine+ clinopyroxene+plagioclase+spinel below 13 kb, (2) clinopyroxene+orthopyroxene+ spinel between 13 kb and 18 kb, (3) clinopyroxene+garnet+spinel above 18 kb. The solidus temperature is slightly below 1,100° at 1 atm, 1,370° at 20 kb, and 1,590° at 40 kb. The primary phase is olivine below 20 kb but is orthopyroxene at 40 kb.In the nepheline basanite, olivine is the primary phase below 14 kb, but clinopyroxene is the first phase to appear above 14 kb. In the alkali-picrite the primary phase is olivine to 40 kb. In the olivine-rich basanite, olivine is the primary phase below 35 kb and garnet is the primary phase above 35 kb. In the olivine-rich alkali basalt the primary phase is olivine below 20 kb and is garnet at 40 kb.Mineral assemblages in a granite-basalt-peridotite join are summarized according to reported experimental data on natural rocks. The solidus of mafic rock is approximately given by T=12.5 P _Kb+1,050°. With increasing pressure along the solidus, olivine disappears by reaction with plagioclase at 9 kb in mafic rocks and plagioclase disappears by reaction with olivine at 13 kb in ultramafic rocks. Plagioclase disappears at around 22 kb in mafic rocks, but it persists to higher pressure in acidic rocks. Garnet appears at somewhat above 18 kb in acidic rocks, at 17 kb in mafic rocks, and at 22 kb in ultramafic rocks.The subsolidus equilibrium curves of the reactions are extrapolated according to equilibrium curves of related reactions in simple systems. The pyroxene-hornfels and sanidinite facies is the lowest pressure mineral facies. The pyroxene-granulite facies is an intermediate low pressure mineral facies in which olivine and plagioclase are incompatible and garnet is absent in mafic rocks. The low pressure boundary is at 7.5 kb at 750° C and at 9.5 kb at 1,150° C. The high pressure boundary is 8.0 kb at 750° C and 15.0 kb at 1,150° C. The garnet-granulite facies is an intermediate high pressure facies and is characterized by coexisting garnet and plagioclase in mafic rocks. The upper boundary is at 10.3 kb at 750° C and 18.0 kb at 1,150° C. The eclogite facies is the highest pressure mineral facies, in which jadeite-rich clinopyroxene is stable.Compositions of minerals in natural rocks of the granulite facies and the eclogite facies are considered. Clinopyroxenes in the granulite-facies rocks have smaller jadeite-Tschermak's molecule ratios and higher amounts of Tschermak's molecule than clinopyroxenes in the eclogite-facies rocks. The distribution coefficients of Mg between orthopyroxene and clinopyroxene are normally in the range of 0.5–0.6 in metamorphic rocks in the granulite facies. The distribution coefficients of Mg between garnet and clinopyroxene suggest increasing crystallization temperature of the rocks in the following order: eclogite in glaucophane schist, eclogite and granulite in gneissic terrain, garnet peridotite, and peridotite nodules in kimberlite.Temperatures near the bottom of the crust in orogenic zones characterized by kyanitesillimanite metamorpbism are estimated from the mineral assemblages of metamorphic rocks in Precambrian shields to be about 700° C at 7 kb and 800° C at 9 kb, although heat-flow data suggest that the bottom of Precambrian shield areas is about 400° C and the eclogite facies is stable.The composition of liquid which is in equilibrium with peridotite is estimated to be close to tholeiite basalt at the surface pressure and to be picrite at around 30 kb. The liquid composition becomes poorer in normative olivine with decreasing pressure and temperature.During crystallization at high pressure, olivine and orthopyroxene react with liquid to form clinopyroxene, and a discontinuous reaction series, olivine orthopyroxene clinopyroxene is suggested. By fractional crystallization of pyroxenes the liquid will become poorer in SiO₂. Therefore, if liquid formed by partial melting of peridotite in the mantle slowly rises maintaining equilibrium with the surrounding peridotite, the liquid will become poorer in MgO by crystallization of olivine, and tholeiite basalt magma will arrive at the surface. On the other hand, if the liquid undergoes fractional crystallization in the mantle, the liquid may change in composition to alkali-basalt magma and alkali-basalt volcanism may be seen at a late stage of volcanic activity.Publication No. 681, Institute of Geophysics and Planetary Physics, University of California, Los Angeles.     

Experimental study of a jotunite (hypersthene monzodiorite): constraints on the parent magma composition and crystallization conditions (P,T, f O 2) of the Bjerkreim-Sokndal layered intrusion (Norway)

The Bjerkreim-Sokndal layered intrusion is part of the Rogaland anorthosite Province of southern Norway and is made of cumulates of the anorthositemangerite-charnockite suite. This study presents experimental phase equilibrium data for one of the finegrained jotunite (Tjörn locality) occurring along its northwestern lobe. These experimental data show that a jotunitic liquid similar in composition to the Tjörn jotunite, but slightly more magnesian and with a higher plagioclase component is the likely parent of macrocyclic units (MCU)III and IV of the intrusion. The limit of the olivine stability field in the experimentally determined phase diagram as well as comparison of the Al₂O₃ content of low-Ca pyroxenes from experiments and cumulates (1.5%) yields a pressure of emplacement 5 kbar. Experimentally determined Fe-Ti oxide equilibria compared to the order of cumulus arrival in the intrusion show that the oxygen fugacity was close to FMQ (fayalite-magnetite-quartz) during the early crystallization. It subsequently decreased relative to this buffer when magnetite disappeared from the cumulus assemblage and then increased until the reentry of this mineral. Calculated densities of experimental liquids show a density increase with fractionation at 7, 10 and 13 kbar due to the predominance of plagioclase in the crystallizing assemblage. At 5 kbar and 1 atm (FMQ-1), where plagioclase is the liquidus phase, density first increases and then drops when olivine (5 kbar) or olivine+ilmenite (1 atm: FMQ-1) precipitate. At 1 atm and NNO (nickel-nickel oxide), the presence of both magnetite and ilmenite as near liquidus phases induces a density decrease. In the Bjerkreim magma chamber, oxides are early cumulus phases and liquid density is then supposed to have decreased during fractionation. This density path implies that new influxes of magma emplaced in the chamber were both hotter and denser than the resident magma. The density contrast inferred between plagioclase and the parent magma shows that this mineral was not able to sink in the magma, suggesting anin situ crystallization process.     

Petrology of the Partridge River Intrusion, Duluth

Drill core DDH-221 was drilled for the Minnamax Project by AMAX Exploration, Inc., as part of the exploration for Cu-Ni sulfidesin the basal rocks of the northwestern margin of the DuluthComplex. The drill core intersects 525 m of the Partridge RiverIntrusion before passing into the Virginia Formation footwall.The rocks in the drill core comprise plagioclase and olivinecumulates, with troctolite and olivine gabbro as the most commonrock types. Sulfide- and oxide-bearing gabbros are present inthe lowest 100 m of the core where decreases in the crystalsizes of plagioclase and olivine, and the appearance of ophitictextures adjacent to the footwall, indicate that the chilledmargin of the intrusion has been preserved (Chalokwu & Grant,1990). The concentrations of incompatible elements in the wholerocks and the iron contents of olivine and pyroxenes all increasesharply in the lowest 100 m of the drill core (Chalokwu &Grant, 1990), and are interpreted as the downward increase inintercumulus liquid now preserved as intercumulus phases, andthe reaction of this liquid with olivine and pyroxenes. Mass, balance calculations for rocks containing widely differentvolumes of intercumulus phases show that the intercumulus liquidwas a chemically uniform ferrodiorite that can be derived fromKeweenawan high-alumina olivine tholeiite by plagioclase (An₆₃),clinopyroxene (En₅₀Fs₁₀Wo₄₀), and olivine (Fo₇₁) fractionation. Initial ⁸⁷Sr/⁸⁶Sr values for plagioclase range between 0–704764and O-706335, with the highest values occurring adjacent tothe footwall Virginia Formation, and the lowest at intermediatedepths in the core. These variations are similar to ⁸⁷Sr/⁸⁶Srvalues reported earlier by Grant & Moiling (1981) From theadjacent core DDH-295, although the values are all greater thanpublished initial ratios for the least altered Keweenawan lavas.We attribute the isotopic variations in core DDH-221 to isotopicheterogeneities in the Partridge River Intrusion magmas, andto limited assimilation of the Virginia Formation within 50m of the footwall. Rare-earth and other trace elements in the intercumulus liquidfrom core DDH-221 have similar distributions to the same elementsin Keweenawan basic to intermediate lavas. We conclude that the rocks of the Partridge River Intrusionsampled in drill core DDH-221 comprise a mechanical mixtureof cumulus plagioclase and olivine and intercumulus liquid thatwere not in equilibrium with each other, and that the intercumulusliquid was broadly consanguineous with Keweenawan high-aluminaolivine tholeiite lavas, but was modified to a greater extentby assimilative exchange with continental crust. After emplacement,the crystal-liquid mixture was modified by flotation of thecumulus plagioclase out of the basal zone, and by limited —but not ubiquitous — assimilation of footwall VirginiaFormation.     

Experimental data at 3 kbars pressure on parental magma to the Bushveld Complex

Experimental studies, mainly under 3 kbars pressure, have been undertaken on representative samples to determine if any of these compositions could be parental magma to the Bushveld Complex. One such composition, with 12.5% MgO, Mg/(Mg + Fe) of 0.72 and quartz-normative, crystallizes olivine, Fo₈₈, as liquidus mineral, at about 1,300° C, followed at only slightly lower temperature by orthopyroxene at 3 kbars pressure. There is a temperature drop of over 100° C before the appearance of plagioclase and finally clinopyroxene. This crystallization sequence is in excellent agreement with the observed sequence in the lower part of the Bushveld Complex.Results at higher pressures show that this composition cannot be a partial melt from mantle peridotite because olivine is replaced by orthopyroxene as the liquidus mineral at lower crustal pressures. A combination of olivine fractionation and contamination was probably involved in the early evolution of this magma.Experimental data on the other compositions show that they are not suitable as parental magma to the lowest portion of the complex. However, the data are used to construct phase diagrams within the basalt tetrahedron at 3 kbars pressure, which are of relevance to the crystallization of basic magmas in the upper crust.Research undertaken at the Grant Institute of Geology, University of Edinburgh, Scotland     

The system diopside-nepheline-leucite

The system diopside-nepheline-leucite, representing a join in the undersaturated part of the system nepheline (Ne)-kalsilite (Ks)-CaO-MgO-SiO₂, has been investigated at atmospheric pressure. The system is pseudoternary and cuts the primary phase volumes of forsterite solid solution (Fo_ss), diopside solid solution (Di_ss), nepheline solid solution (Ne_ss), carnegieite solid solution (Cg_ss), and leucite solid solution (Lc_ss). Melilite (Mel) occurs as a subliquidus phase. The phase diagram has two four-phase points: 1. one at 1275±5° C and Di₆₀Ne₈Lc₃₂ where liquid coexists with Fo_ss, Di_ss and Lc_ss, corresponding to olivine (Ol) leucitite; 2. the other at 1194±5° C and Di_27.5Ne_29.5Lc₄₃ where Ne_ss, Fo_ss and Lc_ss coexist with liquid, corresponding to Ol-Ne italite. With decreasing temperature, liquid moves from point (1) to a five-phase assemblage (3) where liquid is in equilibrium with Fo_ss, Di_ss, Mel and Lc_ss (1258±5°C), which is representative of Ol-Mel-leucitite. From point (2) liquid moves to a second five-phase assemblage (4), where Fo_ss, Mel, Ne_ss, Lc_ss and liquid are in equilibrium (1175±5°C, corresponding to a Lc-Ne katungite. The assemblage Fo_ss+Ne_ss+Di_ss+Mel+Lc_ss+ liquid, is reached between 1168° and 1100° C and corresponds to Ol-Mel-Ne leucitite. Fo_ss reacts with liquid and disappears. Near the point (1) it disappears at 1135±10° C, whereas near the point (2) it reacts out at 1060±10° C. Near the join Di-Ne it disappears at 950±10° C. The final assemblage in the system is representative of Mel-Ne leucitite.Presented at the symposium Recent Advances in the Studies of Rocks and Minerals at High Pressures and Temperatures held in Montreal, 1972. Jointly sponsored by the International Mineralogical Association and the Commission on Experimental Petrologie.     

Ultramafic and mafic xenoliths from Hierro,Canary Islands: evidence for melt infiltration in the upper mantle

Three groups of ultramafix xenoliths were collected from alkali basalt in the island of Hierro, Canary Islands: (1) Cr-diopside series (spinel harzbugite, lherzolite, dunite); (2) Al-augite series xenoliths (spinel wherlite, olivine clinopyroxenite, dunite, olivine websterite); (3) gabbroic xenoliths. The main textures are granoblastic, porphyroclastic and granular, but poikilitic textures, and symplectitic intergrowths of clinopyroxene (cpx) + spinel (sp)±orthopyroxene (opx)±olivine (ol) (in rare cases cpx+opx), occur locally. Textural relations and large inter- and intra-sample mineral chemical variations testify to a complex history of evolution of the mantle source region, involving repeated heating, partial melting, and enrichment associated with infiltration by basaltic melts. The oldest assemblage in the ultramafic xenoliths (porphyroclasts of ol+opx±sp±cpx) represents depleted abyssal mantle formed within the stability field of spinel lherzolite. The neoblast assemblage [ol+cpx+ sp±opx±plagioclase (plag)±ilmenite (il)±phlogopite (phlog)] reflect enrichment in CaO+Al₂O₃+Na₂O+ FeO±TiO₂±K₂O±H₂O through crystal/liquid separation processes and metasomatism. The Al-augite-series xenoliths represent parts of the mantle where magma infiltration was much more extensive than in the source region of the Cr-diopside series rocks. Geothermometry indicates temperature fluctuations between about 900–1000 and 1200°C. Between each heating event the mantle appears to have readjusted to regional geothermal gradient passing 950°C at about 12 kbar. The gabbroic xenoliths represent low-pressure cumulates.     

Petrology of a leucogabbroic interval within basal layered gabbros at North Arm Mountain,Bay of Islands ophiolite

Data from detailed sample traverses in the layered gabbro unit of the North Arm Mauntain massif, Bay of Islands ophiolite, allow meter-scale resolution of magmatic processes in spreading ridge magma chambers. One suite of 46 samples from a 195 m interval near the base of the layered gabbro unit contains cumulus plagioclase (An_73.7–87.5; average modal abundance=75%), clinopyroxene (Mg#=80.3–86.0; 18%), and olivine (Fo_76.6–82.1; 6%), with intergranular orthopyroxene (Mg#=78.0–83.3; 1%), and accessory Cr-Al spinel (Cr#=32.3–41.4). Ilmenite rims spinel in one sample. Whole rock Zr contents range from <6 to 15 ppm. Plots of stratigraphic height in the traverse versus petrogenetic indicators (e.g. Mg#'s of mafic phases and An in plagioclase) reveal both normal and reverse cryptic variation patterns; the patterns for all indices are generally correlated. The normal portions of the patterns formed during fractional crystallization of basalt batches. Ranges of mineral compositions in the normal trends suggest that 29–38% crystallization of each batch of basalt occurred before magmatic replenishment. The reverse cryptic trends formed by crystallization of hybrid magmas produced during periods of magma mixing. Other evidence for magma mixing is the systematic association of spinel and reversely zoned plagioclase with the reverse trends. Experiments and observations of natural assemblages indicate that 55% modal plagioclase crystallizes from basalts at the olivine+plagioclase+clinopyroxene+liquid piercing point. The average plagioclase content of this suite of leucogabbros from North Arm Mountain is too high to have formed from simple crystallization at the piercing point. Petrologic modeling indicates the leucogabbros may have formed from basalts into which a small amount (<10%) of plagioclase was resorbed during mixing; the initial compositions of these hybrid basalts lie in the plagioclase primary phase volume. Other suites of layered gabbros from North Arm Mountain are not so plagioclase-rich as the leucogabbros described above. Crystallization of basalts in the plagioclase primary phase volume and the consequent formation of plagioclaserich gabbros may occur in restricted portions of zoned magma chambers underlying oceanic spreading centers, or may occur episodically in the overall lifetimes of the magma chambers.     

Fluid inclusions as petrogenetic indicators in granulite xenoliths,Pali-Aike volcanic field,Chile

Granulite xenoliths within alkali olivine basalts of the Pali-Aike volcanic field, southern Chile, contain the mineral assemblage orthopyroxene + clinopyroxene + plagioclase + olivine + green spinel. These granulites are thought to be accidental inclusions of the lower crust incorporated in the mantle-derived basalt during its rise to the surface. Symplectic intergrowths of pyroxene and spinel developed between olivine and plagioclase imply that the reaction olivine+plagioclase = Al-orthopyroxene + Al-clinopyroxene + spinel (1) occurred during subsolidus cooling and recrystallization of a gabbroic protolith of the granulites.Examination of fluid inclusions in the granulites indicates the ubiquitous presence of an essentially pure CO₂ fluid phase. Inclusions of three different parageneses have been recognized: Type I inclusions occur along exsolution lamellae in clinopyroxene and are thought to represent precipitation of structurally-bound C or CO₂ during cooling of the gabbro. These are considered the most primary inclusions present. Type II inclusions occur as evenly distributed clusters not associated with any fractures. These inclusions probably represent entrapment of a free fluid phase during recrystallization of the host grains. IIa inclusions are found in granoblastic grains and have densities of 0.68–0.88 g/cm³. Higher density (=0.90–1.02 g/cm³) IIb inclusions occur only in symplectite phases. Secondary Type III CO₂+glass inclusions with =0.47–0.78 g/cm³ occur along healed fractures where basalt has penetrated the xenoliths. Type III inclusions appear related to exsolution of CO₂ from the host basalt during its ascent to the surface. These data suggest that CO₂ is an important constituent of the lower crust under conditions of granulite facies metamorphism, indicated by Type I and II fluid inclusions, and of the mantle, as indicated by Type III inclusions.Correlation of fluid inclusion densities with P-T conditions calculated from both two-pyroxene geothermometry and reation (1) indicate emplacement of a gabbroic pluton at 1,200–1,300° C, 4–6 kb; cooling was accompanied by a slight increase in pressure due to crustal thickening, and symplectite formation occurred at 850±35° C, 5–7 kb. Capture of the xenoliths by the basalt resulted in heating of the granulites, and CO₂ from the basalt was continuously entrapped by the xenoliths over the range 1,000–1,200° C, 4–6 kb. Examination of fluid inclusions of different generations can thus be used in conjunction with other petrologic data to place tight constraints on the specific P-T path followed by the granulite suite, in addition to indicating the nature of the fluid phase present at depth.     

Geology of the mineralized zone of the Wanapitei complex,Grenville Front,Ontario

The Wanapitei Complex (6 km×2.5 km), lying 0.4 km southeast of the Grenville Front, consists of a northwestern zone of gabbro and folded injection breccia and a southeastern layer of intensely folded hornblendeplagioclase gneiss. Disseminated Ni-Cu sulphides are unevenly distributed in a zone between the injection breccia and the folded gneiss.Rocks of the mineralized zone occur in southeastern and northeastern areas. The former area consists of hornblende norite, the major host rock of the sulphides, and olivine norite. Steeply-dipping cross-bedded primary layers and chemical trends indicate the top faces southeast. In the latter area olivine norite, hornblende norite, and hornblende gabbro grade eastward into recrystallized rocks and breccia. The olivine norites are characterized by corona reaction rims. Reactions are: olivine+plagioclase bronzite+diopside-spinel; olivine+pyroxene bronzite; and pyroxene+plagioclase diopside-spinel. Molecular proportion ratio variation diagrams suggest that rocks evolved from a common parent magma that underwent fractionation dominated by olivine and plagioclase. Sulphide mineralization (pyrrhotite, chalcopyrite, pentlandite, pyrite) is interstitial to the silicates and appears to be of primary magmatic origin.Northeasterly-trending shear zones, felsic dikes, and matic dikes are metamorphosed to the same degree as the rocks they cut (amphibolite facies). The sequence of events for the mineralized zone are: intrusion deep in the crust; tilting; brecciation; shearing; felsic and mafic dike emplacement; metamorphism; and injection of granite pegmatite dikes.Deceased (8-16-1986)     

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano,Hawaii

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K₂O in plagioclase and the abundances of TiO₂ and Fe₂O₃in spinel of xenoliths and mid-ocean ridge basalt, and a single ⁸⁷Sr/ ⁸⁶Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155°–230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10^–3–1.91×10^–3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel.     

Petrology of the Proterozoic Potato River Layered Intrusion, Northern Wisconsin, USA

The Potato River intrusion is a Keweenawan (1100 Ma) mafic plutonemplaced in Keweenawan volcanics and earlier Proterozoic metasedimentaryrocks along the southeastern flank of the Lake Superior syncline.It comprises the following lithostratigraphic zones: a thinto absent Border zone of altered olivine gabbro; a Lower zoneof olivine gabbro; a Picritic zone of picrite and troctolite;a Middle zone of olivine gabbro and leucogabbro; an Upper zoneof quartz leucogabbro and ferrogabbro; and a Roof zone of granophyricand granitic rocks. Fractional crystallization is evident fromcompositional changes in the rocks and cumulus minerals withstratigraphic height. Elements concentrated in the cumulus mineralsolivine and plagioclase (Mg, Fe²⁺, Al, Ca, Ni, Co, Cr, Sr) decreasewith height; elements concentrated in the trapped liquid (Na,K, La, Y, Zr, Nb, Rb, Ba) increase with height; and other elements(Ti, Fe³⁺, P, Ga, V, Sc, Cu, Zn) show complicated behavior relatedto the appearance of additional cumulus phases such as clinopyroxene,Fe-Ti oxides, and apatite. Lower zone rocks contain some sulfide,probably from sulfur derived from the country rock, and theUpper zone has sulfides probably precipitated from an immisciblesulfide liquid. The sulfide-bearing rocks have similaritiesto those of other intrusions, such as Bushveld, Stillwater,and Skaergaard. The picritic and troctolitic rocks of the Picritic zone indicatethat the intrusion was open to additional injections of maficmagma. Roof zone granophyric rocks are residual liquids intrudedalong the upper margin of the intrusion during regional tilting,but Roof zone granitic rocks are probably melted country rock.An attempt is made to estimate by reverse stratigraphic summationthe compositional path of the magma that solidified above thePicritic zone. The first compositions are highly aluminous,which suggests that the upper part of the intrusion has beenenriched in plagioclase by convection-aided crystal sorting.A complementary unit of mafic rocks is not exposed, but it couldbe present down dip. Some of the later compositions are similarto typical Keweenawan high-Al tholeiites. The magma did notundergo extreme iron enrichment, probably because of oxygenfugacity buffering.     

The influence of primary magma composition,H2O and pressure on mid-ocean ridge basalt differentiation

MORB suites display variations in their chemical differentiation trends which are closely related to the incompatible element enrichment of the basalts. We examine suites of primitive to evolved basalts from the Pacific-Nazca Ridge at 28° S (mostly depleted); from the Juan Fernandez microplate region (depleted) and from the Explorer Ridge, northeast Pacific (mostly enriched). Trends for incompatible element enriched MORBs consistently show less depletion of Al₂O₃ and less enrichment of FeO when plotted on MgO variation diagrams.Least squares modeling indicates that enriched basalts have undergone less plagioclase crystallization than depleted basalts especially in the early stages of differentiation. Using thermodynamic modelling, we show that variations between MORB differentiation trends result largely from differences in the major element chemistry and H₂O content of primary magmas. Our chosen enriched and depleted near-primary magmas are similar in major element chemistry but the enriched near-primary magma has higher H₂O and lower Al₂O₃ than the depleted near-primary magma. The MORB crystallization sequence is: olivineolivine+plagioclase olivine+plagioclase+high-Ca pyroxene; and the separate and combined effects of lower Al₂O₃ and higher H₂O are to cause plagioclase to crystallize later (lower temperature), and to make the interval of olivine+plagioclase crystallization shorter. As a result, enriched differentiates have higher Al₂O₃ and lower FeO than depleted MORBs at a given MgO content, even though their parents' Al₂O₃ is lower. Crystallization of enriched basalts at higher pressure than depleted basalts is not able to account for differences between the differentiation trends because the proportion of plagioclase is higher during three-phase crystallization at high pressure.The variations in trends do not depend on geographic location and thus are superimposed on any regional variations in MORB chemistry or mantle source. Nor are they related to spreading rate. Depleted basalts from the fast-spreading 28° S and Juan Fernandez ridges have differentiation trends similar to depleted basalts from the medium-spreading Galapagos Spreading Center, whereas differentiation trends for enriched basalts from the medium-spreading Explorer Ridge are quite different. Fe³⁺/Fe_total is similar (and quite low) for enriched and depleted basalts, indicating that neither oxidation state nor early magnetite crystallization are important.     

Diversity and spatial zonation of volcanic rocks from the East Pacific Rise near 21° N

A substantial range of petrologic rock types has erupted on the accreting plate boundary near 21° N on the East Pacific Rise (EPR). Young olivine basalts have Fo_89-86 phenocrysts, low bulk TiO₂ (1.1–1.3%), Ba (7–10 ppm), and high Ni contents (>100 ppm). Older plagioclase-olivine-pyroxene (POP) basalts have Fo_86-81 phenocrysts, high TiO₂ (1.4–1.7%), Ba (9–40 ppm), and low Ni (<100 ppm). The youngest olivine basalts erupt immediately around a segmented axial fissure system. Progressively older, more fractionated POP basalts have spread farther from the same fissure system, producing a stratigraphically-controlled zonal pattern of basalt type distribution around the eruptive fissures. A topographic and morphologic en echelon displacement of the ridge axis fissure of 1.7 km to the NW near 20°54N offsets this zonal distribution pattern. Low pressure crystal fractionation of olivine, plagioclase, and clinopyroxene (251) from an olivine basalt parent would yield POP basalts of the observed Zr, Ti, Y, P and major element chemistry. However very incompatible elements Ba and K are too variably enriched in POP basalts for this model to be viable. Small, variable degrees of mantle partial melting is not a viable model either because of the substantial depletion of Ni which correlates with incompatible element enrichment and because of the precise low pressure cotectic character of POP basalts. The in situ fractionation model of Langmuir (1987) can explain these features. The relative abundance of fractionated lavas, their small-scale areal chemical zonation, the petrochemical correlation between types, and geophysical evidence point to the existence of shallow fractionating magma reservoirs beneath the EPR at 21° N.