Two different crystallization trends of pyroxene in a tholeiitic dolerite,Semi, northern Japan

Compositional and textural relations of coexisting augite and pigeonite in a tholeiitic dolerite in Semi, northern Japan have been analysed with the electron probe microanalyser. Two different crystallization trends of augite have been recognized. In the first case, augite varies in composition from Ca₃₇ Mg₄₁ Fe₂₂ to Ca₃₅ Mg₃₂ Fe₃₃ with nearly constant Ca/Ca +Mg+Fe ratio, whereas in the second case, augite varies from Ca₃₆Mg₄₀Fe₂₄ to Ca₂₈Mg₃₅Fe₃₇ with a considerable decrease of Ca/Ca+Mg+Fe ratio. The compositional trend of augite in the first case may be explained by cotectic crystallization of augite and pigeonite, and that in the second case may be explained by metastable crystallization of subcalcic augite due to undercooling of magma. Such metastable crystallization may have resulted in local heterogeneity of magma.     

Mineralogy as a function of depth in the prehistoric Makaopuhi tholeiitic lava lake,Hawaii

The electron probe X-ray microanalyzer has been used to determine the compositional variability of the groundmass minerals and glass in 10 specimens from a complete 225-foot section of the prehistoric tholeiitic lava lake of Makaopuhi Crater, Hawaii. The order of beginning of crystallization was: (1) chromite, (2) olivine, (3) augite, (4) plagioclase, (5) pigeonite, (6) iron-titanium oxides and orthopyroxene, (7) alkali feldspar and apatite, and (8) glass.Although the lake is chemically tholeiitic throughout, the occurrence of ferromagnesian minerals is as though there were a gradation from alkali olivine basalt in the upper chill downwards to olivine tholeiite. Groundmass olivine decreases downwards and disappears at about 20 feet. Pigeonite is absent in the uppermost 5±2 feet, then increases in amount down to 20 feet, below which augite and pigeonite coexist in constant 21 proportions. Strong zoning and metastable compositions characterize the pyroxenes of the chilled zones, but these features gradually disappear towards the interior of the lake to give way to equilibrium pyroxenes. Relatively homogeneous poikilitic orthopyroxene ( Ca₄Mg₇₀Fe₂₆) occurs in the olivine cumulate zone, having formed partly at the expense of pre-existing olivine, augite, and pigeonite ( Ca₈Mg₆₆Fe₂₆). The growth of orthopyroxene is believed to have been facilitated by the slower cooling rate and higher volatile pressure at depth, and by the rise in Mg/Fe ratio of the liquid due to the partial dissolution of settled olivine.Unlike olivine and pyroxene, feldspar is least zoned in the upper and lower chilled regions. The greatest range of compositional zoning in feldspar occurs at 160 to 190 feet, where it extends continuously from Or_1.0Ab₂₂An₇₇ to Or₆₄Ab₃₃An₃. The feldspar fractionation trend in the An-Ab-Or triangle gradually shifts with depth toward more equilibrium trends, even though the zoning becomes more extreme. The variation with depth in the initial (core) composition of the plagioclase suggests the influence of either slow nucleation and growth (undercooling) or slow diffusion in the liquid, relative to the rate of cooling.Idiomorphic opaque inclusions in olivine phenocrysts are chrome-spinels showing continuous variation from 60 percent chromite to 85 percent ulvospinel and to magnetite-rich spinel. A pre-eruption trend of increasing Al with decreasing Cr can be recognized in chromites from the upper chill. Most of the inclusions show a trend of falling Cr and Al, toward an ulvospinelmagnetite solid solution which is progressively poorer in Usp with depth. This trend was produced by solid state alteration of the chromite inclusions during cooling in the lava lake. Ilmenite (average Ilm₉₁Hm₉) coexists with variably oxidized titaniferous magnetite in the basalt groundmass. Estimated oxygen fugacities agree well with other independent determinations in tholeiitic basalt. No sulfide phase has been detected.Fractional crystallization produced a groundmass glass of granitic composition. Average, in percent, is: SiO₂, 75.5; Al₂O₃, 12.5; K₂O, 5.7; Na₂O, 3.1; CaO, 0.3; MgO, 0.05; total FeO, 1.2; and TiO₂, 0.8. Normative Or> Ab. Minor changes in glass composition with depth are consistent with a greater approach towards the granite minimum. Incipient devitrification precluded reliable analysis of glass from the lower half of the section. The SiO₂-phase associated with devitrification contains alkalis and Al and is believed to be cristobalite. Needle-like apatite crystals in the groundmass glass are Siand Fe-bearing fluorapatites containing appreciable rare earths (predominantly Ce) and variable Cl.The grain-size and maximum An content of the cores of plagioclase grains were controlled by cooling rate and are at a maximum at the center of the section. The most homogeneous pyroxene (and olivine, Moore and Evans, 1967), most equilibrium pyroxene trends, most abundant alkali feldspar, and most equilibrium feldspar trends are found at 160 to 190 feet, which is appreciably below that part of the lake which was slowest to crystallize. Volatile pressure, increasing with depth, possibly controlled the degree of attainment of equilibrium more than cooling rate.Since they are dependent on cooling history, some of the modal criteria commonly used for recognizing basalt types, such as the absence of Ca-poor pyroxene, presence of groundmass olivine, and the presence of alkali feldspar, should be applied with caution. Petrographic comparison of basalts from one flow, volcano, or province, with another, should recognize the possible variations due to cooling history alone.Publication authorized by the Director, U.S. Geological Survey     

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.     

The Salt Lick Creek layered intrusion,East Kimberley region,Western Australia

The Lower Proterozoic Salt Lick Creek intrusion, East Kimberley region, Western Australia, is a layered intrusion divisible into two well-defined zones, the Basal and Main Zones, whose combined stratigraphic thickness, as now exposed, is approximately 1000 metres. The Basal Zone, 360 metres thick, contains three members, two of which (Members 1 and 3) are dominated by olivine, plagioclase cumulates (including harrisites and allivalites); Member 2, near the middle of the Basal Zone, consists substantially of more olivine-rich cumulates, including plagioclase-bearing dunites. The Main Zone, commencing with Member 4 plagioclase, orthopyroxene cumulates, is composed largely of anorthositic cumulates of Member 5. Mild but nevertheless measurable rhythmic layering is superimposed upon the three members comprising the Basal Zone. Electron probe microanalyses of the primary phases across some 500 metres of cumulates indicate limited cryptic variation with stratigraphic height. Olivine ranges in composition from Fo₈₁ to Fo₈₄, orthopyroxene from Ca₂Mg₈₃Fe₁₅ to Ca₂Mg₇₈Fe₂₀, clinopyroxene from Ca₄₈Mg₄₆Fe₆ to Ca₄₄Mg₄₈Fe₈, and plagioclase from An₈₄ to An₈₈ but mineral compositions are not a simple function of stratigraphic height. It is inferred that the parental magma(s) was high-alumina mafic, intrinsically subalkaline, strongly olivine- and plagioclase-normative and in all likelihood tholeiitic in its affinities. The olivine-free cumulates of the Main Zone display a higher level of normative saturation than the cumulates of the Basal Zone but mineral and host rock chemistries, particularly 100 Mg/ (Mg+Fe²⁺) atomic ratios, are not favourable to proposals which would relate the origin of the Main Zone or the several members of the intrusion to the differentiation of a single pool of magma. It is suggested that the Main Zone, at least, derived from a separate pulse of relatively more saturated magma and that the lateral replenishment by more or less undifferentiated magma was also a fundamental and critical factor in the genesis of the Basal Zone cumulates.     

Clinopyroxenes in the tawhiroko tholeiitic dolerite at Moeraki,north-eastern Otago,New Zealand

Clinopyroxenes from various lithologic units in a single tholeiitic dolerite intrusion 50 m thick were analysed with the electron microprobe. Microphenocrysts of augite in the chilled marginal rock have the least scattered CaMgFe ratios, around Ca₃₈Mg₅₀Fe₁₂, and lowest Ti/Al ratios, less than 1/4, of the augites examined; they crystallized prior to emplacement. The augites which crystallized in situ are more Fe-rich and have higher Ti/Al ratios, close to 1/2. Pigeonite started crystallizing later than augite and formed rims to augite crystals. Continuous zoning from augite to subcalcic augite as was previously reported by Benson (1944) for the same dolerite is not observed. Subcaloic ferroaugites, however, link augite and ferropigeonite in the outermost margins of pyroxenes in the later segregations. The small scale differentiation in situ gave rise to globules, veins, and pegmatoids, in which sector-zoning of augite is well developed. The {100} sectors are enriched in MgSiO₃, FeSiO₃, and MnSiO₃ components relative to the {010} and the {110} sectors, and are accordingly depleted in other components. The protosite theory of sector-zoning formation proposed by Nakamura (1973) is further developed and the environment which favours the development of sector-zoning is discussed. The formation of augite rims around quartz-rich xenoliths and the compositional characteristics of the augites concerned are due to local high silica activities. Comments are made concerning some lunar pyroxenes in the light of the present study.     

The detailed mineralogy and significance of an Olivine-two pyroxene gabbro nodule from lanzarote,Canary Islands

A gabbro inclusion typical of the gabbroic xenolith suite in alkalic basalts on Lanzarote is composed of essentially four minerals. Olivine (5 vol.%) and plagioclase An₈₁ (60%) were first to crystallize. The olivine, Fo₇₆ with 0.02% CaO, was subsequently subjected to high-temperature oxidation followed by hydrolysis, resulting in its partial alteration to Fo₉₂ and Fe-oxide-hydroxide plus (free?) silica. Clinopyroxene (30%) Ca₄₃Mg₄₆Fe₁₁ has exsolved orthopyroxene Ca_1.6Mg_76.0Fe_22.4 with 2.10% A1₂O₃ in lamellae ∥ {100}. Orthopyroxene (5%) of the same composition also occurs as discrete crystals and petrographic and chemical criteria suggest that it formed by reaction of olivine with melt. The xenolith probably crystallized from a tholeiitic melt at a depth less than 9 km, i.e. above the Moho discontinuity under Lanzarote. The existence of basalts of olivine-tholeiitic chemistry on Lanzarote suggests a source for the gabbro nodules. Separation of calcic plagioclase from a tholeiitic melt may explain the relatively high alkali contents (Na₂O+ K₂O= 3.2 to 3.7%) of the Lanzarote olivine-tholeiitic basalts.     

The petrology and petrogenesis of the Tertiary anorogenic mafic lavas of Southern and Central Queensland,Australia — Possible implications for crustal thickening

The Miocene-Oligocene volcanism of this region is part of the larger Tertiary volcanic province found throughout E. Australia. Within the S.E. Queensland region, the volcanism is strongly bimodal, and has emanated from six major centres, and many additional smaller centres. The mafic lavas (volumetrically dominant) range continuously from ne-normative through to Q-normative and are predominantly andesine-normative; Mg/Mg+Fe (atomic ratios range from 30–60; K₂O ranges from 0.42–2.93%, and TiO₂ from 0.81–3.6%.Phenocryst contents are low (averaging 6.7 vol.%), and comprise olivine (Fa_18–75; Cr-spinel inclusions occur locally in Mg-rich phenocrysts), plagioclase (An_25–68), and less commonly augite, which is relatively aluminous in lavas of the Springsure volcanic centre. Very rare aluminous bronzite occurs in certain Q-normative lavas. Groundmass minerals comprise augite, olivine (Fa_33–77), feldspar (ranging from labradorite through to anorthoclase and sanidine), Fe-Ti oxides, and apatite. Within many of the Q-normative lavas, extensive development of subcalcic and pigeonitic pyroxenes occurs, and also relatively rarely orthopyroxene. Mineralogically, the ne- and ol-normative lavas, and some of the Q-normative lavas are indistinguishable, and in view of the gradations in chemistry, the term hawaiite has been extended to cover these lavas. The term tholeiitic andesite is used to describe the Q-normative lavas containing Ca-poor pyroxenes as groundmass phases.Megacrysts of aluminous augite, aluminous bronzite, olivine, ilmenite, and spinel sporadically occur within the lavas, and their compositions clearly indicate that they are not derived from the Upper Mantle. Rare lherzolite xenoliths are also found.The petrogenesis of these mafic lavas is approached by application of the thermodynamic equilibration technique of Carmichael et al. (1977), utilizing three parental mineral assemblages that could have been in equilibrium with the magmas at P and T. The models are: (a) standard upper mantle mineralogy; (b) an Fe-enriched upper mantle model (Wilkinson and Binns 1977); (c) lower crust mineralogy, based on analysed megacryst compositions. The calculations suggest that these mafic magmas were not in equilibrium with either mantle model prior to eruption, but show much closer approaches to equilibrium with the lower crust model. Calculated equilibration temperatures and pressures (for the lower crust model) range from 995°–l,391° C (average 1,192), and 7.2–16.3 kb (average 12.4). These results are interpreted in terms of a model of intrusion and magma fractionation within the crust-mantle interface region, with consequent crustal underplating and thickening beneath the Tertiary volcanic regions. Some support for the latter is provided by regional isostatic gravity anomalies and physiographic considerations.     

An analytical electron microscopic study of a pyroxene-amphibole intergrowth

Samples of a garnet granulite from the mafic border units of the Lake Chatuge, Georgia alpine peridotite body were found to contain lamellar intergrowths of a pargastic amphibole in augite having the typical appearance of an exsolution feature. Single crystal X-ray diffraction, optical, electron microprobe and conventional and analytical electron microscopic studies have provided data limiting the compositions and structures of the coexisting phases. Individual lamellae of both materials are from 0.5 to 2.0 m in width with the lamellar interface parallel to {0 1 0}. The formulae of the minerals, as determined by a combination of electron microprobe and analytical electron microscopy, are (Na_0.1Ca_1.0Mg_0.6Fe³⁺ _0.3)(Si_1.8Al_0.2)O₆ for the pyroxene and Na_0.7Ca_1.9(Mg_2.1Fe²⁺ _1.4Fe³⁺ _0.5Ti_0.1Cr_0.1Al_0.8)(Si_5.9Al_2.1) O₂₂(OH)₂ for the amphibole. Several other studies have described intergrowths similar to those observed in this work, in general favoring exsolution as the formation mechanism for the intergrowths. In the Lake Chatuge samples however, replacement of pyroxene by amphibole is in part indicated by continuous gradation of amphibole lamellae into amphiboles rimming the clinopyroxenes.Contribution No. 368 from the Mineralogical Laboratory, Department of Geological Sciences, The University of Michigan, Ann Arbor, Michigan     

Contributions to the mineral chemistry of Hawaiian rocks

Phenocryst and groundmass pyroxenes in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively by electron microprobe. Results and conclusions: i) Tholeiites contain augite, pigeonite, and bronzite; alkalic rocks contain salite, augite, and ferroaugite; and nephelinic rocks have salite, sometimes of Wo>50 mole %. ii) The three suites can be distinguished by Ca contents of pyroxenes: High-Ca pyroxenes of tholeiitic rocks have Wo_30–40; those of alkalic rocks have Wo_38–48; and those of the nephelinic rocks have Wo_47–51; i.e. Wo in clinopyroxene increases from tholeiitic, to alkalic, to nephelinic suites, iii). In the alkalic suite, rock types can be distinguished on the basis of clinopyroxene composition: Alkalic olivine and alkalic basalts have Wo_38–45, hawaiites and mugearites have Wo_45–48. Trachytes can be distinguished from both groups by higher Fe (Fs_22–30) and Ca contents (Wo_43–47). iv) Pyroxenes in tholeiitic rocks show higher intrarock variability (e.g. Fs₁₂Wo₄₀-Fs₃₇Wo₃₀) than those of the alkalic and nephelinic suites, v) Na₂O bulk-rock content affects Na₂O content of the precipitating high-Ca pyroxene; e.g. Na₂O in groundmass pyroxene increases from tholeiitic, to alkalic (mafic members only), to nephelinic suites; a similar relationship is present within the differentiated alkalic suite, vi) In tholeiites, changes in groundmass high-Ca pyroxene compositions are related to changes in bulk rock compositions, e.g. FeO/FeO+MgO+CaO in clinopyroxene increases as this ratio increases in the bulk rock; this is not true for alkalic and nephelinic rocks, vii) In groundmass high-Ca pyroxene, Al₂O₃, Na₂0, and TiO₂ contents increase and MnO content decreases with increasing Wo content from tholeiitic, to alkalic (mafic members only), to nephelinic suites, viii) Groundmass high-Ca pyroxenes are richer in MnO and Na₂O and poorer in Cr₂O₃ compared to coexisting phenocrysts. High-Ca pyroxene phenocrysts in nephelinic rocks and in one mugearite are depleted in SiO₂ and enriched in Al₂O₃ relative to coexisting groundmass clinopyroxene, indicating increased SiO₂ activity during crystallization. Some tholeiites show the reverse; this Si—Al relationship is not clear in other samples.     

Experimental petrology of alkalic lavas: constraints on cotectics of multiple saturation in natural basic liquids

Experimental study of natural alkalic lava compositions at low pressures (pO₂QFM) reveals that crystallization of primitive lavas often occurs in the sequence olivine, plagioclase, clinopyroxene, nepheline without obvious reaction relation. Pseudoternary liquidus projections of multiply saturated liquids coexisting with plagioclase (±olivine±clinopyroxene±nepheline) have been prepared to facilitate graphical analysis of the evolution of lava compositions during hypabyssal cooling. Use of (TiAl₂)(MgSi₂)_–1 and Fe³⁺ (Al)_–1 exchange components is a key aspect of the projection procedure which is succesful in reducing a wide range of compositions to a systematic graphical representation. These projections, and the experiments on which they are based, show that low pressure fractionation plays a significant role in the petrogenesis of many alkalic lava suites from both continental and oceanic settings. However, the role of polybaric fractionation is more evident in the major element chemistry of these lava suites than in many tholeiitic suites of comparable extent. For example, the lavas of Karisimbi, East Africa, show a range of compositions reflecting a polybaric petrogenesis from primitive picrites at 1360° C/18 kb and leading to advanced low pressure differentiates. Evolved leucite-bearing potassic members of this and other suites may be treated in a nepheline-diopside-kspar (+olivine+leucite) projection. Compositional curvature on the plagioclase+clinopyroxene+olivine+leucite cotectic offers a mechanism to explain resorption of plagioclase in alkalic groundmass assemblages and the incompatibility of albite and leucite. This projection is useful for evaluating the extent of assimilation of the alkalic portions of crustal granulites. Assimilation appears to have played some role in the advanced differentiates from Karisimbi.     

Compositions of immiscible liquids in volcanic rocks

Immiscible liquids, preserved as chemically distinct, glassy globules, (Si-rich and Fe-rich) occur in many tholeiitic basalts and some alkaline and calcalkaline lavas. The glasses typically form part of a dark mesostasis containing skeletal magnetite crystals. In thick flows, the Si-rich liquid may crystallize to granophyric patches, and the Ferich one to aggregates of hedenbergite, magnetite, and accessory phases. The mesostases containing these immiscible phases constitute from 20% of a primitive olivine tholeiite (MgO=7.5%) to 50% of a highly fractionated quartz tholeiite (MgO=2.8%), but may be less if the rock is oxidized. Abundant ferric iron promotes early crystallization of magnetite and prevents the iron enrichment necessary to reach the immiscibility field; thus, aa flows rarely exhibit immiscibility, whereas the more reduced pahoehoe ones do.Alumina and alkalis are concentrated in the Si-rich liquid, whereas the remainder of the major elements are concentrated in the Fe-rich melt; but the partitioning of Fe, Mg, Ca, and P is less pronounced in alkaline rocks than in tholeiites. Conjugate liquids have compositions of granite and Fe-rich pyroxenite, though the Si-rich melt in alkaline rocks is more syenitic and the Fe-rich one contains considerable normative alkali feldspar. The liquids coexist with plagioclase and augite of, respectively, An₅₀ and Ca₃₄Mg₁₉Fe₄₇ compositions in tholeiites, and An₄₀ and Ca₄₂Mg₂₉Fe₂₉ in alkaline rocks. Immiscibility is not restricted to K-rich residual liquids, but the miscibility gap is narrower for Na-rich compositions. In tholeiitic basalts with 52% SiO₂, the Na₂O/K₂O ratios in conjugate liquids are equal, but at lower silica contents the Si-rich liquid is relatively more sodic, whereas at higher silica contents it is relatively more potassic. This may explain the association of sodic granites with mid ocean ridge basalts.Immiscible liquids are present in sufficient amounts in so many volcanic rocks that magma unmixing should be considered a viable means of differentiation during the late stages of fractionation of common magmas, at least at low pressures.     

Pyroxenes from the Beaver Bay gabbro complex of Minnesota

Although the Beaver Bay ferrogabbro is a small-scale layered intrusion, Ca-rich pyroxenes show a strong iron enrichment during fractionation, ranging from augite (Mg₃₈Fe₂₄ Ca₃₈) to ferrohedengergite (Mg₁₀Fe₄₈Ca₄₂). Ca-poor pyroxenes from intermediate pigeonite (Mg₃₉Fe₅₀Ca₁₁) to ferriferous pigeonite (Mg₂₇Fe₆₅Ca₈) occur as intercumulus minerals. The pyroxenes from the non-layered Beaver River gabbro are included in the overall pyroxene fractionation trend of the Beaver Bay gabbro complex. The pyroxene trend of the Beaver Bay gabbro complex is similar to those of the Skaergaard and Bushveld; however, there is a slight difference in that the Ca-rich pyroxenes of Beaver Bay (having Mg content over 30%) are slightly richer in Ca than either the Skaergaard or Bushveld augites.     

Amphibole-plagioclase equilibria: An empirical model for the relation albite+tremolite=edenite+4 quartz

Equilibria between plagioclase, calcic amphibole and quartz can be described, in part, by the relation among mineral components: NaAlSi₃O₈+Ca₂Mg₅Si₈O₂₂(OH)₂ = NaCa₂Mg₅AlSi₇O₂₂(OH)₂+4SiO₂; this relation governs the partitioning of Na between plagioclase and the A-site of coexisting amphibole. Data from natural amphibolites reveal that this partitioning is systematic and sensitive to metamorphic grade. The ideal portion of the equilibrium constant (K _id = X _{Na, A}/X_{, A} · X _Ab) derived from natural samples is sensitive to bulk composition, inasmuch as both plagioclase and amphibole are highly non-ideal. Samples from a single outcrop have values ranging from 0.5 (X _Ab=0.74) to 4.1 (X _Ab=0.10). The continuous reaction, NaAlSi₃O₈+Ca₂Mg₅Si₈O₂₂(OH)₂ = NaCa₂Mg₅AlSi₇O₂₂(OH)₂+4SiO₂, proceeds to the right with increasing grade of metamorphism and for a given bulk composition, K _id increases with increasing temperature. Two related discontinuous reactions, actinolite+albite=hornblende+oligoclase+quartz and actinolite+oligoclase=hornblende+anorthite+quartz, also proceed to the right with increasing metamorphic grade and result in changes in the topology of a phase diagram that describes the partitioning of Na between plagioclase and amphibole A-site. A Schreinemakers' net is presented that is consistent with natural occurrences. The results of this study should aid in the delineation of metamorphic facies within amphibolites.     

The morphology and chemistry of K-feldspar megacrysts from Ikizdere Pluton: evidence for acid and basic magma interactions in granitoid rocks, NE-Turkey

Ikizdere Pluton consists of granite, granodiorite, tonalite, monzonite, quartz monzonite containing pinkish colored K-feldspar megacrysts (KFMs). The crystal sizes of the KFMs range from 1 to 4 cm. The lath-shaped megacrysts are uniformly (i.e., randomly) distributed in the host plutonic rocks and have mafic and felsic inclusions whose crystal sizes are smaller than 1 mm. The crystal inclusions are biotite, slightly annitic in composition with X_Mg[=Fe_tot/(Fe_tot+Mg)]=0.50-0.58, amphibole (magnesio-hornblende, X_Mg[=Mg/(Mg+Fe_tot)]=0.70-0.79), iron-titanium oxide (low titanium magnetit and ilmenite), plagioclase (Ab₇₅₋₂₅An₆₅₋₃₅) and as minor quartz. The compositions of the KFMs range from Or₉₅Ab₅An₀ to Or₈₂Ab₁₇An₁. BaO contents of the megacrysts increase from core to rim. The mafic and felsic inclusions are compositionally similar those of the host rocks.The chemical and textural features of K-feldspar are typical for megacrysts that grew as phenocrysts in dynamic granitoidic magma systems. The overgrowth of KFMs and mafic magma injections (magma mixing) may be related to temperature, pressure and compositional fluctuations in the magma chamber. Remnant of earlier formed K-feldspar crystals remain in the felsic magma system, while the mafic injection can decompose some earlier precipitated KFMs. The remnant of K-feldspar remaining after mafic injection are overgrown by rapid diffusion of Ba, K and Na elements in liquid phase, during the later stages of crystallization of the host magma.     

A petrological study of the younger Tongan andesites and dacites,and the olivine tholeiites of Niua Fo'ou Island,S. W. Pacific

Basaltic andesites are the dominant Tongan magma type, and are characterized by phenocrysts of augite, orthopyroxene (or rarely pigeonite), and calcic plagioclase (modally most abundant phase, and interpreted as the liquidus phase). The plagioclase phenocrysts exhibit slight oscillatory reverse zoning except for abrupt and thin more sodic rims, which are interpreted to develop during eruptive quenching. These rim compositions overlap those of the groundmass plagioclase. The pyroxene phenocrysts also exhibit only slight compositional zoning except for the outermost rim zones; the compositions of these rims, together with the groundmass pyroxenes, vary throughout the compositional range of subcalcic augite to ferroaugite through pigeonite to ferropigeonite, and are interpreted in terms of quench-controlled crystallization. This is supported, for example, by the random distribution of Al solid solution in the groundmass pyroxenes, compared to the more regular behaviour of Al in the phenocryst pyroxenes. The analysed Niua Fo'ou olivine tholeiites are aphyric; groundmass phases are plagioclase (An_17–88), olivine (Fa_18–63), titanomagnetite (usp. _59–73), and augite-ferroaugite which does not extend to subcalcic compositions; this is interpreted to be due to higher quenching temperatures and lower viscosities of these tholeiites compared to the basaltic andesites.Application of various geothermometers to the basaltic andesites suggest initial eruptive quenching temperatures of 1,008–1,124 ° C, plagioclase liquidus temperatures (1 bar) of 1,210–1,277 ° C, and orthopyroxene-clinopyroxene equilibration of 990–1,150 ° C. These calculated temperatures, together with supporting evidence (e.g. absence of olivine and amphibole, liquidus plagioclase, and plagioclase zoning patterns) are interpreted in terms of phenocryst crystallization from magmas that were either strongly water undersaturated, nearly anhydrous, or at best, water saturated at very low pressures (< 0.5 kb). This interpretation implies that these Tongan basaltic andesites did not originate by any of the currently proposed mechanisms involving hydrous melting within or above the Benioff zone.     

Simulation of primary phase relations and mineral compositions in the Partridge River intrusion,Duluth Complex,Minnesota: implications for the parent magma composition

In order to describe the composition and crystallinity of the initial (parental) magma of the Partridge River intrusion of the Keweenawan Duluth Complex, and thereby understand the mode of emplacement and solidification of the intrusion, we have applied a numerical simulation technique called geochemical thermometry (Frenkel et al. 1988). The parental magma was a low-alumina, high-Ti-P olivine tholeiite similar to typical Keweenawan low-alumina, high-Ti-P basalts associated with the Duluth Complex and from the nearby Portage Lake area of the Lake Superior region. The parental magma was emplaced as a crystal-liquid suspension, followed by chilling of an evolved, leading edge ferrodioritic liquid in the basal zone of the intrusion. The conditions of emplacement at the present crustal location were 1,150°C, 2 kbar, and f _{O 2} slightly above the wustite-magnetite (WM) buffer. The main differentiation process after emplacement was the sorting and redistribution of plagioclase and olivine crystals on a local scale accompanied by less efficient convection and minor settling of olivine. Calculated crystallization sequence for the parental magma is olivine+plagioclase (1,240°C)olivine+plagioclase+magnetite (1,146°C, WM+0.5)olivine+plagioclase+magnetite+augite (1,140°C, WM+0.5). The calculated compositions of the cumulus olivine and plagioclase in equilibrium with the parent magma at 1,150°C are Fo_66.7±1.1 and An_64.5±2.5, respectively, and are similar to the estimated average composition of primary olivine (Fo_69.1±2.8) and the average composition of plagioclase core (An_66.3±2.8) measured in drill core samples through the intrusion (Chalokwu and Grant 1987).     

Abyssal tholeiites from the Oceanographer Fracture Zone

Fresh basalts from the Oceanographer Fracture Zone are petrographically and chemically similar to typical abyssal tholeiites, but are somewhat enriched in large ion lithophile elements, with consistent differences among separate dredge hauls. Olivine compositions are in equilibrium with host basalt for reasonable K _D values, but some plagioclases are anomalously calcic (e.g., a rock highly differentiated in Mg/Mg+Fe bears some plagioclase of An₈₆). Ti/Al in clinopyroxene is approximately constant at 1/6, but Ti+Al abundance decreases in the sequence basalt groundmass cpx, basalt phenocryst+microphenocryst cpx, gabbro cpx (samples from adjacent dredges), an effect that may be related to decrease in cooling rate. Least-squares calculations indicate that 45% of magma with the composition of the more primitive sample must be removed as plagioclase, clinopyroxene and olivine (in the ratio 4.42.71, respectively) to obtain the composition of the more differentiated sample. Both samples have excess plagioclase on the liquidus, however, which should not be the case for the differentiated composition if it is produced by fractionation of all three phases. The excess of plagioclase and the anomalous plagioclase compositions indicate that the samples cannot be related solely by fractional crystallization. Additional processes such as magma mixing or plagioclase accumulation (or both) must have effected these differences.     

Petrography and mineral chemistry of neovolcanics occurring between Pacific and Nazca Plate boundaries

Mid-Oceanic Ridge Basalt (MORB) samples collected from southern East Pacific Rise (SEPR) have been investigated. These highly phyric plagioclase basalts (HPPB) and moderately phyric plagioclase basalts (MOPB) show rare cumulate and vitrophyric textures with plagioclase (>10% as phenocryst) and abundant glass (>72%). Electron Probe Micro Analysis (EPMA) showed large compositional variations in the megacrysts as well as microcrysts of plagioclase (An₆₂ to An₈₂), olivine (Fo₇₈ to Fo₈₇), pyroxene (ferroaugite to augite) and iron oxides, mostly titaniferous magnetite. Olivine grains show high Mg# (>80%) and distinctly low in NiO (0.01–0.2%). Ferroan trevorite (NiO =16.22 and FeO_(t) =83.06) a characteristic meteoritic mineral has been identified from the olivine megacrysts of MORB, possibly attributed to Ni-enrichment, resulted from heterogeneity of the lower mantle. Wide range of An composition in plagioclase is indicative of large pressure range of crystal nucleation under decompression at a depth of ∼70 km (An₈₂) up to the ocean spreading centre. Absence of zoning observed in all the minerals present in the MORB samples, possibly attributed to unmixing and dominant fractionation process.     

Tholeiitic basalt magmatism of Mount Etna and its relations with the alkaline series

Mount Etna is composed for the most part of intermediate alkaline products, most of them porphyritic-the etnaïtes-, that may be defined as sodic trachybasalts or trachyandesites. The strato-volcanio itself overlies tholeiitic basalts (usually aphyric, except for olivine) belonging to three major types: olivine tholeiites (normative Ol+Hy; modal olivine and augite, titanomagnetite and ilmenite), pigeonite tholeiites (normative Hy+minor Ol or Qz; modal pigeonite and augite with minor olivine, ilmenite and titanomagnetite), transitional tholeiites, i.e. transitional between pigeonite tholeiites (aphyric) and alkali basaltic etnaïtes (porphyritic, with normative Ol+Ne or minor Hy; modal augite and olivine, titanomagnetite alone). An analcite basalt, chemically close to alkali basaltic etnaïtes, forms the small Cyclopean Islands, SE of Etna, and an alkali olivine basalt composes a neck at Paterno, SW foot of Etna.Both pigeonite tholeiites and alkali basaltic etnaïtes may be derived from a primitive olivine tholeiite magma by subtraction or addition of phases crystallized at moderate and low pressure (kaersutite±olivine, calcic plagioclase and clinopyroxene). The differentiation process implies crystal fractionation of the primitive olivine tholeiite magma at varying levels of the crust. The speed of ascent of the magma is thought to be the factor controlling the level at which differentiation may take place: in low velocity regimes, fractionation takes place at deeper levels of the crust. Slow ascent speeds would be the consequence of a developing crustal extension episode, induced by mantle diapirism that generated the olivine tholeiite magma below the Mount Etna area.