Komatiitic and Iron-rich Tholeiitic Lavas of Munro Township, Northeast Ontario

Munro Township, in the Archean Abitibi greenstone belt of northeastOntario, contains volcanic and hypabyssal rocks of two magmaseries: (1) an Fe-rich tholeiitic series of basaltic to daciticlava flows (3–10 m thick), layered peridotite-pyroxenite-gabbroflows (120 m thick), and layered sills (700 m thick); (2) anultramafic-mafic komatiitic series, comprising discrete lavaflows of peridotitic to andesitic composition (1–17 mthick), layered peridotite-gabbro flows (120 m thick), and layeredsills (500 m thick). The komatiitie lavas form a successionabout 1000 m thick that is both underlain and overlain by thickersuccessions of tholeiitic volcanic rocks. Three types of komatiite are recognized: peridotitic, pyroxenitic,and basaltic komatiites. The most ultramafic are peridotiticcumulates rich in forsteritic olivine (Fo_89–94), at thebases of flows and sills. Many less mafic peridotitic komatiites(MgO: 20–30 per cent), which typically form the upperparts of flows and the marginal parts of small intrusions, exhibitspinifex textures indicative of their formation from ultrabasicliquids. Pyroxenitic komatiites (MgO: 12–20 per cent)also may contain olivine, but are dominated by clinopyroxene,usually in spinifex textures. Basaltic komatiites (MgO <12per cent) are composed mainly of clino-pyroxene and plagioclaseor devitrified glass, rarely in spinifex texture and more commonlyin equigranular textures. Peridotitic komatiite with roughly30 per cent MgO appears to represent a parental liquid fromwhich the more ultramafic komatiites formed by accumulationof olivine, and the less mafic types were derived by fractionationof olivine, joined and finally succeeded in later stages byclinopyroxene and plagioclase. Komatiites of Munro Township share many of the characteristicsof the komatiites from the Barberton Mountain Land, South Africa(Voljoen & Viljoen, 1969a and b), but lack the high CaO/Al₂O₃ratios that distinguish the Barberton rocks. The Munro komatiitesare identical in this respect to ultramafic volcanic rocks inAustralia, Canada, Rhodesia, and India. It is proposed thatthe definition of the term komatiite be broadened so that itincludes all members of this ultramafic-mafic rock series, notonly those from Barberton Mountain Land. The proposed criteriaare: (1) highly ultramafic compositions in noncumulate lavas;(2) unusual volcanic structures such as spinifex texture andpolyhedral jointing; (3) low Fe/Mg ratios at given Al₂O₃ valuesor high CaO/Al₂O₃ ratios; low TiO₂ at given SiO₂; and high MgO,NiO, and Cr₂O₃.     

桂北四堡群中科马提岩系及其成因类型

桂北四堡群中许多镁铁质—超镁铁质岩体,实际上是火山岩或次火山岩。有的还具有科马提岩岩流的结构分层,其堆积带上部橄榄石和辉石晶体间隙中充填有基质物质。这些基质中发育了典型的橄榄石鬣刺结构。科马提岩与其伴生玄武岩属具成因联系的同一演化系列。在微量元素及REE特征上,区内科马提岩具有较好的Ⅱ类科马提岩属性,它们系亏损地幔经较小程度部分熔融产生。     

Crystallization Orders and Phase Chemistry of Glassy Lavas from the Pillow Sequences, Troodos Ophiolite, Cyprus

Three genetically unrelated magma suites are found in the extrusivesequences of the Troodos ophiolite, Cyprus. A stratigraphicallylower pillow lava suite contains andesite and dacite glassesand shows the crystallization order plagioclase; augite, orthopyroxene;titanomagnetite (with the pyroxenes appearing almost simultaneously).These lavas can in part be correlated chemically and mineralogicallywith the sheeted dikes and the upper part of the gabbro complexof the ophiolite. The second magma suite is represented in astratigraphically upper extrusive suite and contains basalticandesite and andesite glasses with the crystallizaton orderchromite; olivine; Ca-rich pyroxene; plagioclase. This magmasuite can be correlated chemically and mineralogically withparts of the ophiolitic ultramafic and mafic cumulate sequence,which has the crystallization order olivine; Ca-rich pyroxene;orthopyroxene; plagioclase. The third magma suite is representedby basaltic andesite lavas along the Arakapas fault zone andshows a boninitic crystallization order olivine; orthopyroxene;Ca-rich pyroxene; plagioclase. One-atmosphere, anhydrous phaseequilibria experiments on a lava from the second suite indicateplagioclase crystallization from 1225?C, pigeonite from 1200?C,and augite from 1165?C. These experimental data contrast withthe crystallization order suggested by the lavas and the associatedcumulates. The observed crystallization orders and the presenceof magmatic water in the fresh glasses of all suites are consistentwith evolution under relatively high partial water pressures.In particular, high P_H2O (1–3 kb) can explain the lateappearances of plagioclase and Ca-poor pyroxene in the majorityof the basaltic andesite lavas as the effects of suppressedcrystallization temperatures and shifting of cotectic relations.The detailed crystallization orders are probably controlledby relatively minor differences in the normative compositionsof the parental magmas. The basaltic andesite lavas are likelyto reach augite saturation before Ca-poor pyroxene saturation,whereas the Arakapas fault zone lavas, which have relativelyless normative diopside and more quartz, reached the Ca-poorpyroxene-olivine reaction surface and crystallized Ca-poor pyroxeneafter olivine.     

Physical volcanology and geochemistry of Palaeoarchaean komatiite lava flows from the western Dharwar craton,southern India: implications for Archaean mantle evolution and crustal growth

ABSTRACT

Palaeoarchaean (3.38–3.35 Ga) komatiites from the Jayachamaraja Pura (J.C. Pura) and Banasandra greenstone belts of the western Dharwar craton, southern India were erupted as submarine lava flows. These high-temperature (1450–1550°C), low-viscosity lavas produced thick, massive, polygonal jointed sheet flows with sporadic flow top breccias. Thick olivine cumulate zones within differentiated komatiites suggest channel/conduit facies. Compound, undifferentiated flow fields developed marginal-lobate thin flows with several spinifex-textured lobes. Individual lobes experienced two distinct vesiculation episodes and grew by inflation. Occasionally komatiite flows form pillows and quench fragmented hyaloclastites. J.C. Pura komatiite lavas represent massive coherent facies with minor channel facies, whilst the Bansandra komatiites correspond to compound flow fields interspersed with pillow facies. The komatiites are metamorphosed to greenschist facies and consist of serpentine-talc ± carbonate, actinolite–tremolite with remnants of primary olivine, chromite, and pyroxene. The majority of the studied samples are komatiites (22.46–42.41 wt.% MgO) whilst a few are komatiitic basalts (12.94–16.18 wt.% MgO) extending into basaltic (7.71 – 10.80 wt.% MgO) composition. The studied komatiites are Al-depleted Barberton type whilst komatiite basalts belong to the Al-undepleted Munro type. Trace element data suggest variable fractionation of garnet, olivine, pyroxene, and chromite. Incompatible element ratios (Nb/Th, Nb/U, Zr/Y Nb/Y) show that the komatiites were derived from heterogeneous sources ranging from depleted to primitive mantle. CaO/Al₂O₃ and (Gd/Yb)_N ratios show that the Al-depleted komatiite magmas were generated at great depth (350–400 km) by 40–50% partial melting of deep mantle with or without garnet (majorite?) in residue whilst komatiite basalts and basalts were generated at shallow depth in an ascending plume. The widespread Palaeoarchaean deep depleted mantle-derived komatiite volcanism and sub-contemporaneous TTG accretion implies a major earlier episode of mantle differentiation and crustal growth during ca. 3.6–3.8 Ga.     

Partial melting and recrystallization of Archeaan komatiites by residual heat from rapidly accumulated flows

Spinifex-textured komatiites at Honeymoon Well, Western Australia, show evidence of partial melting and recrystallization of original igneous textures. Their textures and mineral compositions differ markedly from those typical of komatiites. Spinifex olivine plates are bent and broken, while interstitial space between spinifex and cumulus olivine is occupied by polygonal aggregates of clinopyroxene, orthopyroxene, minor olivine and plagioclase. Similar granular pyroxene-plagioclase aggregates occur as diffuse veins cutting spinifex zones and cumulate zones of the flows and, in places, form the matrix to a breccia containing corroded fragments of spinifex rock. Thermometry based on the two pyroxene assemblages yields temperatures of 1055° to 1141° C, just below the low-pressure komatiite solidus. Mineral compositions are different from those of typical komatiites: clinopyroxenes are Al-poor and Cr-rich, olivines are unusually iron-rich and depleted in Cr and Ca, and the low-Ca pyroxene is bronzite rather than the more typical pigeonite. We interpret these observations as the results of thermal metamorphism, partial remelting and subsequent slow crystallization of originally normal spinifex-textured komatiite flows. The rocks in question occupy a 40–70 m interval sandwiched between two olivine-rich units: an underlying 90 m-thick olivine adcumulate layer, forming part of the cumulate zone of a basal 160 m-thick flow, and an overlying 1 km-thick extrusive body composed mostly of olivine mesocumulate and adcumulate and capped in turn by spinifex-textured flows. Thermal modelling shows that a sinusoidal temperature profile of cool flow tops and hot flow centres would exist within this sequence shortly after eruption. Conductive thermal relaxation of this profile could reheat spinifex zones to the extent of inducing partial melting and textural reconstitution. Such reheating is largely dependent on the time interval between the emplacement of successive flows. Calculations suggest that at Honeymoon Well the emplacement interval must have been of the order of 10 years or less. Textural reconstitution may have contributed to the development of the thick orthocumulate sequences characteristic of komatiites in the Agnew-Wiluna belt. Present address: Geochemex Australia, P.O. Box 281, West Perth, 6005, Western Australia     

Low- and high-alumina komatiites from a Late Archaean sequence,Newton Township,Ontario

Late Archaean komatiitic lavas from Newton Township, Ontario, consist of 6 chemically distinct magma types: 3 komatiites and 3 komatiitic basalts. The succession is unusual in containing both Al- and HREE-depleted komatiites and Al- and HREE-undepleted komatiites. The two types form distinct stratigraphic units separated by komatiitic basalts. Two komatiite types are strongly LREE depleted, whilst the third and the associated komatiitic basalts range from mildly depleted to enriched. Of the six magma types, only the two strongly LREE depleted komatiites represent primary mantle melts. The other komatiite type and the komatiitic basalts were derived from the primary komatiite magmas by combinations of olivine (+chromite) fractionation, assimilation of continental crust, and magma mixing. The two primary magmas may have been derived from similar sources, their contrasting chemistry being due to differing degrees of garnet segregation during melting. A generally applicable conclusion is that a wide range of komatiitic magma types can be generated from a relatively homogeneous depleted mantle, under conditions likely to prevail during the eruption of late Archean greenstone belt sequences.     

Bizarre geochemistry of komatiites from the Crixás greenstone belt,Brazil

Komatiite lava flows in the Crixás greenstone belt, Goiás, Brazil, have textures and volcanic structures typical of Archean komatiites, but are geochemically most unusual. The flows are porphyritic and massive, or layered with spinifex upper parts and olivine cumulate lower parts. MgO contents range from 18 to 40%. In such lavas, only olivine (and minor chromite) can have crystallized, but neither major nor trace elements fall on olivine control lines. In MgO variation diagrams, CaO and Sr fall on lines with slopes steeper than olivine control lines; SiO₂, FeO, Na₂O, K₂O and Y show little systematic variation; Zr shows a large variation that does not correlate with MgO; and Al₂O₃ decreases markedly with decreasing MgO. The aberrant behaviour is highlighted by the REE (rare earth elements) in spinifex and olivine cumulate layers from three flows: in the spinifex layers, chondrite-normalized REE patterns are hump-shaped with maxima at Nd or Sm ((La/Sm)_N=0.6, (Gd/Yb)_N=1.6–2.3), whereas cumulate zones in the same flows have steadily sloping patterns, with LREE enriched relative to HREE ((La/Sm)_N=1.3, (Gd/Yb)_N=1.4). Neither normal magmatic processes acting during emplacement of the komatiites, nor thermal erosion and wall-rock assimilation can explain these effects, and we speculate that elements commonly thought of as “immobile” (e.g. Al, Zr, REE) migrated during hydrothermal alteration or metamorphism. A Pb-Pb whole rock isochron gave an age of 2,728±140 Ma and selected Sm-Nd analyses an apparent isochron age of 2,825±98 Ma (ɛ_Nd≈0). The Pb-Pb age is believed to be the approximate time of emplacement. Interpretation of the Sm-Nd data is complicated by the evidence of mobility of REE.     

Magnesium and iron isotopes in 2.7 Ga Alexo komatiites: Mantle signatures, no evidence for Soret diffusion, and identification of diffusive transport in zoned olivine

Komatiites from Alexo, Canada, are well preserved and represent high-degree partial mantle melts (∼50%). They are thus well suited for investigating the Mg and Fe isotopic compositions of the Archean mantle and the conditions of magmatic differentiation in komatiitic lavas. High precision Mg and Fe isotopic analyses of 22 samples taken along a 15-m depth profile in a komatiite flow are reported. The δ²⁵Mg and δ²⁶Mg values of the bulk flow are −0.138 ± 0.021‰ and −0.275 ± 0.042‰, respectively. These values are indistinguishable from those measured in mantle peridotites and chondrites, and represent the best estimate of the composition of the silicate Earth from analysis of volcanic rocks. Excluding the samples affected by secondary Fe mobilization, the δ⁵⁶Fe and δ⁵⁷Fe values of the bulk flow are +0.044 ± 0.030‰, and +0.059 ± 0.044‰, respectively. These values are consistent with a near-chondritic Fe isotopic composition of the silicate Earth and minor fractionation during komatiite magma genesis. In order to explain the early crystallization of pigeonite relative to augite in slowly cooled spinifex lavas, it was suggested that magmas trapped in the crystal mush during spinifex growth differentiated by Soret effect, which should be associated with large and coupled variations in the isotopic compositions of Mg and Fe. The lack of variations in Mg and Fe isotopic ratios either rules out the Soret effect in the komatiite flow or the effect is effaced as the solidification front migrates downward through the flow crust. Olivine separated from a cumulate sample has light δ⁵⁶Fe and slightly heavy δ²⁶Mg values relative to the bulk flow, which modeling shows can be explained by kinetic isotope fractionation associated with Fe-Mg inter-diffusion in olivine. Such variations can be used to identify diffusive processes involved in the formation of zoned minerals.     

Petrogenesis of olivine-phyric shergottites Sayh al Uhaymir 005 and Elephant Moraine A79001 lithology A

Martian meteorites Sayh al Uhaymir (SaU) 005 and lithology A of EETA79001 (EET-A) belong to a newly emerging group of olivine-phyric shergottites. Previous models for the origin of such shergottites have focused on mixing between basaltic shergottite-like magmas and lherzolitic shergottite-like material. Results of this work, however, suggest that SaU 005 and EET-A formed from olivine-saturated magmas that may have been parental to basaltic shergottites.SaU 005 and EET-A have porphyritic textures of large (up to ∼3 mm) olivine crystals (∼25% in SaU 005; ∼13% in EET-A) in finer-grained groundmasses consisting principally of pigeonite (∼50% in SaU 005; ∼60% in EET-A), plagioclase (maskelynite) and < 7% augite. Low-Ti chromite occurs as inclusions in the more magnesian olivine, and with chromian ulvöspinel rims in the more ferroan olivine and the groundmass. Crystallization histories for both rocks were determined from petrographic features (textures, crystal shapes and size distributions, phase associations, and modal abundances), mineral compositions, and melt compositions reconstructed from magmatic inclusions in olivine and chromite. The following observations indicate that the chromite and most magnesian olivine (Fo 74-70 in SaU 005; Fo 81-77 in EET-A) and pyroxenes (low-Ca pyroxene [Wo 4-6] of mg 77-74 and augite of mg 78 in SaU 005; orthopyroxene [Wo 3-5] of mg 84-80 in EET-A) in these rocks are xenocrystic. (1) Olivine crystal size distribution (CSD) functions show excesses of the largest crystals (whose cores comprise the most magnesian compositions), indicating addition of phenocrysts or xenocrysts. (2) The most magnesian low-Ca pyroxenes show near-vertical trends of mg vs. Al₂O₃ and Cr₂O₃, which suggest reaction with a magma. (3) In SaU 005, there is a gap in augite composition between mg 78 and 73. (4) Chromite cores of composite spinel grains are riddled with cracks, indicating that they experienced some physical stress before being overgrown with ulvöspinel. (5) Magmatic inclusions are absent in the most magnesian olivine, but abundant in the more ferroan, indicating slower growth rates for the former. (6) The predicted early crystallization sequence of the melt trapped in chromite (the earliest phase) in each rock produces its most magnesian olivine-pyroxene assemblage. However, in neither case is the total crystallization sequence of this melt consistent with the overall crystallization history of the rock or its bulk modal mineralogy.Further, the following observations indicate that in both SaU 005 and EET-A the fraction of solid xenocrystic or xenolithic material is small (in contrast to previous models for EET-A), and most of the material in the rock formed by continuous crystallization of a single magma (possibly mixed). (1) CSD functions and correlations of crystal size with composition show that most of the olivine (Fo 69-62 in SaU 005; Fo 76-53 in EET-A) formed by continuous nucleation and growth. (2) Groundmass pigeonites are in equilibrium with this olivine, and show continuous compositional trends that are typical for basalts. (3) The CSD function for groundmass pigeonite in EET-A indicates continuous nucleation and growth (Lentz and McSween, 2000). (4) The melt trapped in olivine of Fo 76 to 67 in EET-A has a predicted crystallization sequence similar to that inferred for most of the rock and produces an assemblage similar to its modal mineralogy. (5) Melt trapped in late olivine (Fo ∼ 64) in SaU 005 has a composition consistent with the inferred late crystallization history of the rock.The conclusion that only a small fraction of either SaU 005 or EET-A is xenocrystic or xenolithic implies that both rocks lost fractionated liquids in the late stages of crystallization. This is supported by: (1) high pigeonite/plagioclase ratios; (2) low augite contents; and (3) olivine CSD functions, which show a drop in nucleation rate at high degrees of crystallization, consistent with loss of liquid. For EET-A, this fractionated liquid may be represented by EET-B.     

Spinifex-textured komatiites in the south border of the Carajas ridge,Selva Greenstone belt,Carajás Province,Brazil

Spinifex-textured komatiites in the Selva greenstone belt are the first unequivocal examples of komatiites in the Transition Subdomain of the Carajás Mineral Province. Outcrops of spinifex-textured komatiites, located ∼1.5 km to the south of the Carajás ridge, were discovered during regional exploration for Ni–Cu–(PGE) sulfide deposits by VALE. They are associated with a 3.8 km long unit consisting of variable types of ultramafic rocks (talc schist, serpentinite and spinifex-textured komatiite). This ultramafic unit follows the steep dipping NW–SE trending Selva greenstone belt composed mainly by quartz-chlorite schists (interpreted as metasediments) and chlorite-actinolite schists (interpreted as metabasalts). Greenschist facies metamorphic parageneses characterize all rock types in the Selva greenstone belt.The komatiitic rocks in the Selva belt comprise a sequence of flows consisting of an upper spinifex-textured layer and a lower olivine cumulate layer. Although the spinifex and cumulus textures are well preserved in the field, the primary mineralogy of the komatiites has been completely replaced by greenschist facies metamorphic minerals. Platy olivine spinifex texture, consisting of an array of roughly parallel olivine plates, and random spinifex texture, consisting of randomly oriented olivine plates, are the most common primary volcanic textures in komatiites in the Selva greenstone belt. Platy and random spinifex texture is defined by former plates of olivine replaced by serpentine with minor actinolite, chlorite and magnetite, alternating with former matrix replaced by abundant actinolite and minor chlorite, talc, serpentine, and magnetite. The domains between olivine plates in both platy and random spinifex-textured rocks contain irregular arrays of fine-grained parallel crystals, representing primary fine-grained “quench” clinopyroxene crystals replaced by actinolite.Spinifex-textured komatiites have MgO contents bracket between 22.8 and 26.9 wt.%, and cumulate textured komatiites have MgO contents up to 40.6 wt.%. When plotted vs MgO contents, most major and minor elements fall on well-defined linear trends indicating control by olivine fractionation or accumulation. Komatiites from the Selva and Seringa (located in the Rio Maria Domain) belts are Al-undepleted with Al₂O₃/TiO₂ ratios close to 20. Results for CaO, Na₂O, and REE suggest that these elements were mobile and their abundances have been modified during metasomatic alteration. REE contents in some samples are very high (up to 40 times primitive mantle values) and REE patterns vary from flat (La/Yb_MN ∼ 1) to highly enriched in LREE (La/Yb_MN up to ∼ 10). The REE mobility may be related to hydrothermal alteration associated to Cu–Au mineralization in the region.The identification of spinifex-textured komatiites close to the Carajás Basin suggests the continuation of 3.0–2.9 Ga greenstone belts of the Rio Maria Domain within the Transition Subdomain, and enlarges the area with potential to host komatiite-associated Ni–Cu–PGE deposits.     

The petrogenesis of the Lac Guyer komatiites and basalts and the nature of the komatiite-komatiitic basalt compositional gap

A sequence of ultramafic rocks in the Lac Guyer Archean greenstone belt exhibit brecciated flow tops, pillow structures, and spinifex textures testifying to their volcanic origin. Massive, spinifex-textured and differentiated flows in the sequence have the chemical characteristics of peridotitic komatiite, with MgO ranging from 19–25 wt.%. Associated pillowed flows have compositions that straddle the conventional boundary between komatiite and komatiitic basalt with MgO contents ranging from 16 to 19 wt.% MgO and are best termed pyroxenitic komatiites. Unlike other komatiitic occurrences, the peridotitic and pyroxenitic komatiites at Lac Guyer constitute a continuous chemical spectrum with no evidence of population minimum near 18 wt.% MgO. The contrasting behaviour of highly compatible elements, such as Ni and Cr, versus incompatible elements, such as Zr, indicate that this compositional spectrum was produced by a variation in the extent of partial melting (10–40%) of a garnet lherzolite source in the Archean mantle. The pyroxenitic komatiites represent liquids produced during lower (10–20%) degrees of melting during which garnet remained in the mantle residue. However, a change in slope in the distribution of Zr vs. Y between the pyroxenitic and the peridotitic komatiites indicates that garnet was completely consumed at the more extensive degrees of melting which produced the peridotitic komatiites. The Lac Guyer volcanic rocks display a population minimum at 15 wt.% MgO separating komatiitic magmas whose compositions are controlled by partial melting from basalts whose composition is controlled by crystal fractionation. The population minimum near 18 wt.% MgO which is taken as the boundary between komatiite and komatiitic basalt may have a similar origin.     

Compositional relations of coexisting orthopyroxene,pigeonite and augite in a tholeiitic andesite from Hakone Volcano

The compositions of five different coexisting pyroxenes hypersthene, pigeonite and augite in groundmass and bronzite and augite of phenocryst in a tholeiitic andesite from Hakone Volcano, Japan have been determined by the electron probe microanalyser. It is shown that there is a compositional gap of about 25 mole per cent CaSiO₃ between groundmass pigeonite and augite, compared with 35 per cent CaSiO₃ between phenocrystic augite and bronzite. Subcalcic augite or pigeonitic augite was not found. The groundmass augite, which occurs only as thin rims of pigeonite and hypersthene, is less calcic and more iron-rich than the phenocryst augite. It is also shown that the groundmass pigeonite is 3–4 mole per cent more CaSiO₃-rich than the coexisting groundmass hypersthene. The Fe/(Mg + Fe) ratios of these coexisting hypersthene and pigeonite are about 0.31 and 0.33, respectively. It is suggested from these results that a continuous solid solution does not exist between augite and pigeonite of the Fe/(Mg + Fe) ratio at least near 0.3 under the conditions of crystallization of groundmass of the tholeiitic andesite. It is suggested from the Mg-Fe partition and the textural relation that the groundmass augite crystallized from a liquid more iron-rich than that from which groundmass hypersthene and pigeonite crystallized.     

Comparison of Archean dunites and komatiites associated with nickel mineralisation in Western Australia: Implications for dunite genesis

The two important classes of Archean Fe-Ni-Cu sulphide deposits in Western Australia are those hosted by (1) coarse-grained adcumulate dunites (e.g. Agnew, Mount Keith) and (2) komatiitic lavas (e.g. Kambalda). Close similarities in compositions of relict olivine, pyroxene, and chromite from dunitic and komatiitic host rocks and compositional and textural similarities between chilled margins of some dunites and some komatiites indicate origins from similar komatiitic liquids which contained 20%–32% MgO. As field relations suggest that the dunites are probably lateral stratigraphic equivalents of spinifextextured komatiites, they are interpreted as the slowcooled end member of a continuum from spinifex-textured komatiites (former liquids) through cumulate komatiites (40%–90% olivine) to adcumulate komatiitic dunite (>90% olivine). Previous classification of these Ni deposits as intrusive- and volcanic-related deposits now appears unwarranted, and the terms komatiitic dunite-hosted and komatiite-hosted deposits are preferred.     

Compositional Zoning in Pyroxenes from Lunar Rock 12021, Oceanus Procellarum

Electron probe study of the pyroxene phenocrysts in rock 12021of the Apollo 12 sample reveals an extraordinary variety ofzoning phenomena. These phenocrysts have cores of relativelyhomogeneous pigeonite which are mantled by Ca-rich pyroxenes;the mantles are zoned outward from about 20 mol per cent FeSiO₃at the core-mantle boundaries to 70 mol per cent FeSiO₃ at themargins of the phenocrysts. The character of the normal zoningdiffers in each growth sector. Four different trends characterizinggrowth on (110), (100), (010), and parallel to c are described.Pronounced but erratic oscillatory effects are impressed onthe normal zoning in all sectors. Normal zoning in lunar pyroxenes is generally more extensivethan in terrestrial pyroxenes, probably because the lunar lavaswere an order of magnitude more fluid than terrestrial basalts.Turbulent flow in lunar lavas may have caused some of the oscillatoryeffects. The cyclic nature of augite and pigeonite crystallizationin these pyroxenes is probably kinetic in origin; conceivablyit could reflect the presence of an augite-pigeonite peritectic.It is likely that further knowledge of the crystal structureof pigeonite at high temperatures will be required before astructural model can be formulated that will satisfactorilyexplain the details of the sector zoning. Coarse-grained pyroxferroite and subcalcic ferroaugite havecrystallized in apparent ‘equilibrium’ in the finalstages of formation of the groundmass in rock 12021. Nevertheless,the crystallization of the pyroxferroite was probably metastablerelative to the assemblage ferroaugite+ fayalite+ tridymite.Data on the effect of Mg substitution on the stability of pyroxferroitewill be needed to establish this point. We suggest that the pigeonite cores of the phenocrysts in rock12021 crystallized under quiescent conditions, probably in amagma chamber below the lunar surface, and that the stronglyzoned augite mantles crystallized during emplacement of thelava on the surface.     

A clinoenstatite-bearing cumulate Olivine Pyroxenite from Howqua,Victoria

The Howqua Olivine Pyroxenite of eastern Victoria, Australia, intrudes a metamorphosed sequence of Cambrian high-Mg lavas. It crystallized an unusual mineral assemblage: Cr-rich magnesiochromite, olivine (Fo₉₄), and protoenstatite (now inverted to polysynthetically-twinned clinoenstatite). Residual liquid crystallized strongly-zoned interstitial pyroxenes followed by pargasite. Pargasite, often showing quench habit, crystallized in interstitial glass which is now altered to serpentine.The extremely refractory nature of the cumulus phases indicates a very high temperature of crystallization for liquidus olivine and chromite from a high-MgO, low-Al₂O₃ parent liquid similar in some respects to Archaean peridotitic komatiites. The suggested origin by hydrous melting of depleted mantle peridotite, plus other compositional and mineralogical similarities (especially the olivine-liquid reaction producing protoenstatite) indicate that the parent magma of the Howqua Olivine Pyroxenite had many features in common with the high-SiO₂, high-MgO clinoenstatite-bearing boninitic lavas of the Western Pacific. It is interpreted as a more extreme melt with affinities to boninite and it demonstrates that ultramafic magmas existed in the Cambrian.     

Low-Pressure Experimental Constraints on the Evolution of Komatiites

Melting experiments were performed on a komatiitic basalt with17 wt% MgO from Munro Township, Ontario, at I-atm pressure andan oxygen fugacity controlled approximately to the fayalite-magnetite-quartzbuffer. The experiments showed that olivine appears at 1344±5°C,spinel at 1334±6°C plagioclase at 1185±5°C,augite at 1176±5°C and pigeonite at 1154±6°C.Compositionally, olivine varies from Fo₉₀ to Fo₇₄ and displaysan average K^Fe/Mg_D (ol/liq) of 0•32. The spinels are chromitesand chromian spinels with Mg/(Mg + Fe²⁺) ratios between 0•66and 0•;32, which show a marked correlation with meltingtemperature. The pyroxenes show an average K^Fe/Mg_D (px/liq)of 0•26, identical for augite and pigeonite. Plagiodaseranges compositionally between An₈₂ and An₇₂ Plotted in thepseudo-quaternary basalt phase diagram, the liquid line of descentis similar to that observed for quartz tholeiitic magmas. Therefore,the low-pressure, late-stage evolution products of komatiiteand basaltic komatiite parental magmas will chemically and mineralogicallybe ferrobasaltic quartz tholeiites. High-temperature and high-pressuremodeling suggests that the main observed compositional variationof Munro komatiites can be explained by low-pressure crystalfractionation and accumulation of olivine into komatiite liquidswith below 21•5–23•5 wt% MgO and eruptive temperaturesbelow 1435–1465°C for oxygen fugacities between thefayalite-magnetite quartz (FMQ) and iron-wiistite (IW) buffers.The maximum magnesium content of liquid komatiites, assumingequilibrium Fo₉₄ olivine, is 27–29 wt% MgO and eruptivetemperatures are between 1515 and 1540°C. KEY WORDS: komatiites; experimental petrology; Munro Township; Ontario     

Differentiation of Komatiite Flows

Although layered komatiite flows with spinifex-textured upperparts and olivine-enriched lower parts are commonly thoughtto provide firm evidence of magmatic differentiation by olivinesettling, there are reasons to suspect that this may not betrue. Komatiite flows almost certainly convect vigorously asthey cool, with convective velocities that greatly exceed thesettling velocities of olivine grains. Other explanations forthe differentiation of komatiite flows into layers with differentolivine contents need to be investigated. One such explanation is provided by a detailed study of a komatiiteflow from Alexo, Ontario, Canada. This flow is about 16 m thickand has a spinifex-textured upper layer, and a lower layer,called the B-layer, which is composed of closely-packed, equantolivine phenocrysts. The composition of the initial liquid inthe flow is given by an upper chill sample, which has 28 percent MgO. In underlying spinifex lavas, MgO contents range from20 to 35 per cent MgO, and the B-layer has about 42 per centMgO. Olivines are most Fo-rich in the chill margin (Fo_94.1)and in the B-layer (Fo_93.8). In spinifex lavas, olivines aregenerally less magnesian, ranging from a high of Fo_93.8 in unusuallyMgO-rich chevron spinifex lavas, down to Fo₈₉ in the lower platespinifex lavas. It is believed that solidification of the upper part of theflow started only after it had become ponded, and that crystallizationproceeded with growth of spinifex olivines downwards from theroof of the flow. The manner in which the composition of silicateliquid within the flow changed during growth of the spinifexlayer can be calculated using the compositions of olivines inspinifex lavas. These calculations show that all the spinifexlavas are more magnesian than the liquids from which they formed:i.e. they all contain a component of excess olivine. Furthercalculations indicate, however, that liquid compositions inthe lower part of the flow changed more rapidly than can beexplained by accumulation of olivine in the spinifex lavas.This additional olivine must have crystallized in the lowerpart of the flow, and remained there as phenocrysts suspendedin the convecting liquid. As the spinifex-textured upper partcontinued to grow and thicken, olivine continued to crystallizewithin the flow, and the growing phenocrysts became more andmore concentrated in an ever-decreasing volume of liquid. Whenthe concentration exceeded about 50 vol. per cent, the viscosityof the lava became high enough to inhibit convection. The flowthen solidified completely, maintaining its olivine distributionwith a spinifextextured upper layer and an olivine-enrichedlower layer.     

Elevation of potassium content of basaltic magma by fractional crystallization: the effect of pressure

A wide range of natural quartz-normative liquids crystallizes olivine at low pressure. Addition of K₂O to the system results in expansion of the olivine primary phase field and replacement of pigeonite (stable in the K-free system) by hypersthene. Some variation in phase relations results from depression of crystallization temperature towards the temperature at which pigeonite reacts to form augite and hypersthene because of addition of K₂O. Another important influence on phase relations results from cation interactions in the liquid related to addition of K₂O. Studies of crystallization behavior of materials similar in most elements except K₂O show that K₂O content markedly alters crystallization behavior for more siliceous liquids but appears to have less effect on liquids with lower SiO₂ contents. Low-Ca pyroxenes melt congruently at P>5 kbar, so anhydrous liquids coprecipitate olivine, plagioclase, and two pyroxenes. Addition of K₂O to the liquid has the same effect as at 1 atm. Hypersthene replaces pigeonite as the Low-Ca pyroxene crystallization from liquids with >1.5% K₂O and the olivine primary phase field grows at the expense of those of pyroxenes and plagioclase. At 10 kbar, olivine may develop a reaction relationship with liquids containing >6% K₂O. At 15 kbar, however, liquids evolve to a pseudoeutectic involving alkali feldspar. The systematic variation in phase relations has important consequences for magmatic evolution in different environments. Dry mafic liquids at shallow levels in oceanic areas can crystallize olivine until the liquid is very evolved, resulting in extreme SiO₂-enrichment besides enrichment in K₂O, and producing potassic dacites. Olivine coexists with liquids with up to 54% SiO₂ if K₂O=0.6% (Grove and Baker 1984) but as much as 63% SiO₂ if K₂O3.5% (Ussler and Glazner 1989). Magmas rising beneath light continental crust may pond at the Moho and evolve to low-density liquids that can rise to the surface. Coprecipitation of olivine, plagioclase, augite, and a low-Ca pyroxene, produces enrichment in K₂O with only slight enrichment in SiO₂. This is terminated, at pressures of 6 to, possibly, 12 kbar, by development of a reaction relationship of olivine and liquid that progresses to higher K₂O contents with pressure. At pressures as high as 15 kbar, the reaction relation may not develop and only crystallization of alkali feldspar suppresses K₂O-enrichment. Any magmatic H₂O or crustal contamination may modify phase relations. The phase relations do, however, suggest that variation in K₂O:SiO₂ of evolved volcanic rocks is related to crustal thickness rather than to variation in the chemical compositions of primary magmas.     

Mineral chemistry of submarine lavas from Hilo Ridge, Hawaii: implications for magmatic processes within Hawaiian rift zones

The crustal history of volcanic rocks can be inferred from the mineralogy and compositions of their phenocrysts which record episodes of magma mixing as well as the pressures and temperatures when magmas cooled. Submarine lavas erupted on the Hilo Ridge, a rift zone directly east of Mauna Kea volcano, contain olivine, plagioclase, augite ±orthopyroxene phenocrysts. The compositions of these phenocryst phases provide constraints on the magmatic processes beneath Hawaiian rift zones. In these samples, olivine phenocrysts are normally zoned with homogeneous cores ranging from ∼ Fo₈₁ to Fo₉₁. In contrast, plagioclase, augite and orthopyroxene phenocrysts display more than one episode of reverse zoning. Within each sample, plagioclase, augite and orthopyroxene phenocrysts have similar zoning profiles. However, there are significant differences between samples. In three samples these phases exhibit large compositional contrasts, e.g., Mg# [100 × Mg/(Mg+Fe⁺²)] of augite varies from 71 in cores to 82 in rims. Some submarine lavas from the Puna Ridge (Kilauea volcano) contain phenocrysts with similar reverse zonation. The compositional variations of these phenocrysts can be explained by mixing of a multiphase (plagioclase, augite and orthopyroxene) saturated, evolved magma with more mafic magma saturated only with olivine. The differences in the compositional ranges of plagioclase, augite and orthopyroxene crystals between samples indicate that these samples were derived from isolated magma chambers which had undergone distinct fractionation and mixing histories. The samples containing plagioclase and pyroxene with small compositional variations reflect magmas that were buffered near the olivine + melt ⇒Low-Ca pyroxene + augite + plagioclase reaction point by frequent intrusions of mafic olivine-bearing magmas. Samples containing plagioclase and pyroxene phenocrysts with large compositional ranges reflect magmas that evolved beyond this reaction point when there was no replenishment with olivine-saturated magma. Two of these samples contain augite cores with Mg# of ∼71, corresponding to Mg# of 36–40 in equilibrium melts, and augite in another sample has Mg# of 63–65 which is in equilibrium with a very evolved melt with a Mg# of ∼30. Such highly evolved magmas also exist beneath the Puna Ridge of Kilauea volcano. They are rarely erupted during the shield building stage, but may commonly form in ephemeral magma pockets in the rift zones. The compositions of clinopyroxene phenocryst rims and associated glass rinds indicate that most of the samples were last equilibrated at 2–3 kbar and 1130–1160 °C. However, in one sample, augite and glass rind compositions reflect crystallization at higher pressures (4–5 kbar). This sample provides evidence for magma mixing at relatively high pressures and perhaps transport of magma from the summit conduits to the rift zone along the oceanic crust-mantle boundary. Received: 8 July 1998 / Accepted: 2 January 1999     

Deciphering an Archean mantle plume: Abitibi greenstone belt,Canada

The 2724–2722 Ma Stoughton-Roquemaure Group (SRG) of the Abitibi greenstone belt (the Archean Superior Province, Canada) is a ≤ 2 km thick komatiite–basalt succession intermittently exposed for about 50 km along strike. The ultramafic and mafic rocks occur mainly as pillowed, brecciated, and massive flows with well preserved spinifex textures in the komatiites. Volcanological, comparative stratigraphic and geochemical studies of the group along a volcanic marker horizon at the base of the succession allow the assessment of magma emplacement processes and mantle source rocks. Major feeder channels, secondary distributary tubes surrounded by pillowed flows with minor breccias and hyaloclastites display facies architecture of small volume flow fields (1–2 km³). Within the SRG, Al-depleted (ADK; Barberton-type) and Al-undepleted (AUK; Munro-type) komatiitic lavas are intercalated with tholeiitic basalt flows at a m- to 10s of m scale. Basalts and komatiites are inferred to be mantle plume-related; both rock types form two groups with characteristics of ADK and AUK including Al₂O₃/TiO₂ ~ 9–12 for ADK versus 17–22 for AUK, as well as (Gd/Yb)_n with > 1.3 versus ~ 1, respectively. The interdigitation of compositionally different flow units, limited extent of SRG volcanic rocks and facies architecture with the prevalence of small volume flows argue for a relatively small, heterogeneous mantle plume during the incipient stage of the evolution of the Archean Abitibi belt. Assuming that the scale of heterogeneities is comparable to the field expression of compositional changes and stratigraphy, it can be suggested that geochemical plume ‘layering’ is on 10s to 100s of m-scale. The evolution of this Archean mantle plume from inception to demise compares favorably with the Yellowstone hotspot which is assumed to have developed over 17 m.y. and had a diameter of about 300 km.