Rapakivi texture from the O’Leary Porphyry,Arizona (U.S.A.)

The rhyodactic O’Leary Porphyry which forms the Pleistocene (0.233±0.37 m.y.) volcanic domes of O’Leary Peak and Darton Dome in the San Francisco Volcanic Field (northern Arizona, U.S.A.) contains sanidine phenocrysts with oligoclase mantles (rapakivi texture). Rapakivi texture occurs worldwide in silicic rocks of many ages and has been attributed to various igneous and metamorphic processes. The O’Leary Porphyry contains both mantled and unmantled sanidine (both are Or_63–69 Ab_30–36An₁), oligoclase and quartz phenocrysts, labradorite (An₅₃Ab₄₅Or₂) and kaersutite xenocrysts and andesite xenoliths. The compositional range of oligoclase is the same (An_11–26Ab_70–80Or_r–10) for the rapakivi mantles, the oligoclase phenocrysts, and the oligoclase crystals poikilitic within sanidines. Most mantles are discontinuous. The sanidine appears to have been resorbed prior to mantling. Experimental melting studies on the O’Leary Prophyry show that, for a 15 wgt.% water system, plagioclase crystallized prior to sanidine and quartz crystallized last. The O’Leary Porphyry, although inhomogeneous, plots on a Q-Or-Ab-An diagram well within the plagioclase stability field. Poikilitic plagioclases within sanidines further support crystallization of plagioclase prior to sanidine in the O’Leary Porphyry. Exsolution of a ternary feldspar to form a plagioclase mantle is the most commonly accepted igneous theory of rapakivi texture formation but has been eliminated as the origin of the O’Leary Porphyry rapakivi. Petrologic models by Tuttle and Bowen and by Stewart are rejected for the O’Leary rapakivi because of inconsistencies with the O’Leary occurrences. Two theories are viable for the O’Leary rapakivi texture. First, is a decrease in water vapor pressure which would enlarge the plagioclase stability field possibility causing mantling of metastable sanidines. The second and preferred theory is that of an addition of sodium and calcium by basification (chemical assimilation without melting) of the xenoliths within the O’Leary Porphyry. This would move the bulk composition of the melt into the plagioclase field possibly resulting in crystallization of plagioclase on sanidine crystals. Diffusion of sodium and calcium from the xenoliths to sanidine would result in mantling only those crystals near to the xenoliths. Later, convection would result in distribution throughout the melt of rapakivi, unmantled sanidines, and xenolithic kaersutite as is seen in the porphyry. Basic xenoliths are extremely common in rapakivi-bearing rocks. Those within the O’Leary Porphyry are andesitic and show resorption, and in some areas of O’Leary Peak itself, have been drawn out into schlieren.     

Nomenclature and petrochemistry of the peralkaline oversaturated extrusive rocks

Four-hundred and twenty-one analyses of quartz-normative, peralkaline, extrusive rocks have been collected from the literature and from unpublished sources and are used to examine chemical variation in this group of rocks. Comparisons are particularly made between the full body of data and the variations recorded in the non-hydrated obsidians alone byMacdonald andBailey (1973). It is argued that the compositions of the magmas which formed these obsidians and those which subsequently crystallised were similar as regards the major oxides SiO₂, Al₂O₃, FeO + Fe₂O₃, Na₂O and K₂O. Marked variations in the abundances of the minor oxides CaO and TiO₂ are shown to be a result of geographical location. Small but significant differences in the distribution of Al and Fe as a function of normative quartz can be recognised between various pantelleritic suites. A new classificatory scheme is proposed, based on the iron (as FeO) and Al₂O₃ contents. This is simpler than previously employed normative classifications, is more applicable to crystalline rocks, and, happily, in 95 % of cases gives the same rock name as the normative system.     

Experimental petrology relating to oversaturated peralkaline volcanics: A review

Experiments specifically devoted to problems of oversaturated peralkaline rocks have been primarily concerned with quartz + feldspar + liquid equilibria, and the determination of the low temperature liquids in the feldspar primary phase region. The results are brought together, and compared with natural compositions, by recalculating and plotting in the system Na₂O-K₂O-Al₂O₃-SiO₂ (molecular). The minimum zone in the peralkaline quartz-feldspar cotectic is the synthetic analogue of most comendites and many pantellerites. Peralkaline trachytes and trachytic pantellerites appear to be the natural equivalents of synthetic low temperature liquids in the feldspar primary phase region, but the more peralkaline liquids cannot be a simple evolutionary series controlled only by feldspar fractionation. Experiments have yet to reveal the relating process (or processes) for the series pantelleritic trachyte to pantellerite. Feldspars separating from low temperature synthetic and natural liquids are usually Or₃₅ ±₅ i.e. equivalent to the composition range of the thermal minimum between the anorthoclase and sanidine solid solution loops in the alkali feldspar join. Such liquids may therefore be envisaged as the locus of compositions in the peralkaline system that are in equilibrium with alkali feldspar at the minimum in the solid solution series. Such feldspar, when it separates from the vast majority of peralkaline liquids is fractionating K₂O and Al₂O₃, making the residual liquids more peralkaline and more sodic. Development of the peralkaline condition in natural liquids is commonly ascribed to the « plagioclase effect », but this creates its own dilemma by seeming to be effective only in liquids which are already distinctively alkaline. Furthermore it can only work in a low pressure regime. Examination of the high pressure melting curves of possible mantle minerals shows that acmitic pyroxenes have the lowest melting, in either hydrous or anhydrous conditions, especially at low partial pressures of oxygen. This provides a simple source control by which liquids will either be intrinsically peralkaline (if the melt volume is small) or inherit the potential for low pressure operation of the « plagioclase effect » (most basic magmas). Alkali transfer is well-attested in solid ? vapour experiments and in natural examples of metasomatic aureoles. The mobility of alkalis (and iron) must figure in any realistic scheme of peralkaline petrogenesis. This points up the need for experiments designed to meet the challenge ofopen system magmatism.     

Magma types of volcanic rocks and continental margin of the Taiwan upper Paleozoic Geosyncline

Greenrocks are very common in the Tananao Schist of eastern Taiwan where the known fossils are of Permian in age. Fourty-four greenrock samples were chemically analysed and their magma types studied. The chemical composition of the greenrocks have marked variation common in volcanic rock series. The greater parts of the greenrocks belong to basalt and a smaller portion to basaltic andesite (SiO₂ 53 %–58 %). They are probably isochemical with their original igneous rocks except for volatile components. No striking Fe-enrichment exists in a MgO-ΣFeO-(Na₂O=K₂O) diagram. Based on (Na₂O=K₂O)-Al₂O₃-SiO₂ diagrams afterKuno (1960), the parent magma of the rocks mostly belong to the high-alumina basalt series and only a few to alkali olivine basalt series. The high-alumina basalt can be looked upon as having an incipient trend for the calc-alkaline or the hypersthene series ofKuno (1959). The average K/Rb ratio of 460, the average TiO₂ percentage of 1.5 %, and low K₂O of around 0.5 % seem to warrant a conclusion that the basaltic rocks were poured out in the upper Paleozoic eugeosyncline on an embryonic continental crust. Considering the rock association of amphibolite plus serpentine (dismembered ophiolite), meta-graywacke, metachert, crystalline limestone, metaarkose, and metabasites in the Tananao Schist, the most probable site for the eugeosyncline may been an extensional trough near the fragmented paleo-Asiatic margin.     

Geochemistry of upper cretaceous volcanic rocks from the pontic chain,northern turkey

Preliminary data on major elements, Cs, Ba, Rb, Pb, Sr, REE, Y, Th, U, Zr, Ht, Sn, Nb, W, Mo, Cr, V, Sc, Ni, Co and Cu contents for eight samples coming from the Upper Cretaceous volcanic belt of the Pontic Chain (Northern Turkey) are reported. SiO, versus K₂O relationship shows that the analyzed samples belong to the calc-alkaline and shoshonite series. The calc-alkaline rocks appear to represent two distinct magma types one close in composition to typical island are calc-alkaline magmas and one with high incompatible elements concentration and tractionated heavy REE patterns which suggest a genesis by partial melting at high pressure with a garnet bearing residue. Shoshonitic rocks show Na₂O/K₂O close to one, high incompatible elements concentration, and TiO₂%. Al₂O₃%, Ni and Co contents, Ni/Co and V/Ni ratios and REE patterns similar to typical island are andesites which suggest for these rocks similar genetical processes as the island are calc-alkaline magmas.     

Petrochemistry of quaternary pumiceous pyroclastic products in southern Guadeloupe (F.W.I.)

Pumiceous pyroclastic products are present as flows and falls at several stages of the evolution of the southern Guadeloupe volcanic island. An understanding of this volcanism had to rely on detailed petrochemical data of these products to complement similar data for effusive rocks so as to yield complete stratigraphical coverage. On the other hand most pumiceous rocks are more or less conspicuousily banded suggesting that mixing phenomena occurred to different degrees in their genesis. Three major classes of pumiceous products are found: (1) the Axial Chain deposits (2.0–0.5 My) are characterized by An90, 75-55 + En55 + Wo42En37 + Usp35-37 ± Fo68 ± Hble, SiO₂ 60%, SiO₂/Th 35.6, and La/Th 3.9. Banded samples have components that differ in evolution indices by about 50%; (2) the Bouillante Chaine pyroclastics (0.3–0.1 My) consist of scattered deposits with variable mineralogical and geochemical compositions that seem to have erupted from a number of small eruptive centers. Qz-dacitic pumice is common with An90, 70-45 + En66-56 + Usp32-38 + Ilm94 + Hble ± Wo40-42En40-42, SiO₂ 62%, SiO₂/Th 22.9, and La/Th >4. Mixed pumice samples have highly contrasted evolution indices differing by up to 120%; (3) the Pintade pumice flows and falls correspond to the major pyroclastic event (approx. 10 km³) in the southern Basse Terre area. They are characterized by An85-70 + En66-56 + Usp32-37 ± Wo42En42, SiO₂/Th 18.7-22?6, and La/Th 3.0-4.0. Banded pumice lumps are scarce and show slight compositional contrasts; differences in evolution indices do not exceed 38%. Axial and Bouillante chain pyroclastics and Grande Découverte volcano pumice respectively, form two different families in trace element plots. Minor elements in pyroxenes also are distinctive. These trends are similar to those obtained for effusive rocks and define comagmatic series. Major and trace element data for the separated components of inhomogeneous pumice in each formation always plot in the corresponding series. These chemical discriminants can be used to attribute samples of unknown provenance to a given volcanic ensemble. An inverse relationship between differences in evolution indices in inhomegeneous pumice and the volume of any single eruptive sequence is noted. This is an indication that pumiceous pyroclastic rocks were erupted from a zoned magma chamber. We favor an interpretation where zonation is produced by influx of less envolved magma in superficial differentiated chambers which is a direct cause for eruption.     

Petrology of tholeiitic lavas from Tanna Island (New Hebrides): Importance of cumulative processes in Island arc magmatism

Tanna, one of the southernmost islands of the New Hebrides volcanic arc, is made of Late Pliocene to Recent island arc tholeiitic basalts and andesites, with SiO₂ contents ranging from 45 to 57%. These lavas are highly porphyritic (30–50% in volume): phenocrysts of plagioclase are the most abundant, together with olivine and clinopyroxene. The groundmass contain plagioclase, augite, olivine, magnetite and glass; pigeonite, tridymite, sanidine and, rarely, biotite may also occur. The olivines and clinopyroxenes show an iron enrichment from the cores of phenocrysts to their rims and the groundmass crystals, but their compositional variations are not correlated with the Mg/Fe ratio of bulk host rocks, the most Fe-rich compositions being found in Mg-rich lavas. Plagioclase compositions range from An₉₅ to An₆₀ in the basalts and An₆₀ to An₅₀ in the andesites, but, within each group, they are not correlated with SiO₂ or Na₂O contents of host lavas. Consequently, the bulk major element compositions of Tanna volcanic rocks cannot be considered as primarily controlled by crystal separation from successive liquids. The oxyde-SiO₂ variations diagrams, and the modal compositions and mineral chemistry show that crystal accumulation is the predominant mechanism accounting for bulk rock compositions. However, this does not exclude fractional crystallization: the variation of the calculated groundmass mineralogy strongly suggest the occurrence of crystal removal mainly clinopyroxene and magnetite.     

Major-element petrochemistry of some extrusive rocks from the volcanically active Mariana Islands

Volcanic rocks from six of the currently or recently active volcances of the Mariana Island are show little variation in major element abundances. SiO₂ content averages 51.5 wt.%. The flows are high in Al₂O (mean 17.7 wt.%) and Fe oxides (mean 10.1 wt.% calculated as FeO only), and moderate in MgO content (mean 4.7 wt.%), Na₂O (mean 2.7 wt.%), and K₂O (mean 0.7 wt.%). Only the rocks from Farallon de Pajaros, the northernmost of the Mariana Islands, deviate slightly from the average of the analyses. Three analyses from this island are slightly higher in SiO₂ (about 54 wt.%) and Al₂O₃, and are lower in total Fe oxides and MgO. According to preferred classification, the lavas of the Mariana Islands can be termed mela-andesites, high-alumina basalts, or calc-alkaline (orogenic) basalts. The K₂O values (mean 0.7 wt.%) obtained from lavas of the Mariana Islands are significantly higher than the K₂O values (about 0.33 wt.%) from volcanics of the Izu chain to the north. Inasmuch as the substantial scatter in location of earthquake foci beneath both arcs prevents accurate delineation of the upper boundary of the Benioff zone, it presently cannot be determined whether this discrepancy in K₂O values reflects a difference in depth from the volcanic are to the dipping seismic zone or relates to other phenomena. The older volcanic islands within the Mariana-Bonin island chain apparently defined an island arc system during Eocene to Miocene time. This indicates that the present plane of convergence between the Pacific plate and the Philippine Sea plate has defined the convergence between these plates since Eocene time.     

Calc-alkaline volcanic rocks from NW Sardinia: Evaluation of a fractional crystallization model

The volcanic centre of Monte Seda Oro, N. W. Sardinia, representative of a Cenozoic calc-alkaline andesitic suite of rocks is composed of a variety of rocks ranging from high alumina basalts to dacites. The minerals of basaltic, andesitic and dacitic rocks show only limited variation in chemical composition. The geochemical data suggest that the various rock-types are related by a crystal-liquid fractionation. Least-squate numerical calculations, using major element data, support the derivation of andesites with SiO₃ content ranging from 53.8 to 59.0% from basalts having about 48.7% of SiO₂ by low pressure crystal fractionation of the phenocryst phases present in these rocks. However, the origin of dacites cannot be readily explained by this mechanism.     

Volcan ceboruco: A major composite volcano of the mexican volcanic belt

Ceboruco is a major composite volcano at the western end of the Mexican Volcanic Belt, near the junction between the North American and Pacific plates. The volcano is built from successive eruptions of andesite lavas and pyroclastic rocks, and major eruptions during its history have resulted in the formation of two concentric calderas. The youngest volcanic activity has included the extrusion of dacites within the inner caldera and a voluminous flank eruption of andesite during 1870–72. Fumarolic activity persists to the present day. Chemical analyses show that the lavas are of cale-alkaline type and rangs from andesite (SiO₂=58–61%) to acid dacite (SiO₂=68%) in composition. The rate of increase of K₂O relative to SiO is greater than that in volcanic rocks from the Mexican Volcanic Belt as a whole. This indicates that simple models based on the application of such relationships may not be adequate to explain the petrogenesis of calc-alkaline lavas.     

Capping volcanic rocks: West central Nevada

Cenozoic capping volcanic rocks in the Nevada portion of the Basin and Range Province of the western United States belong to the high alumina calcalkaline igneous series. Varying proportions of plagioclase (An=85 to 45 percent), pyroxene (augite, pigeonite, and hypersthene), olivine, magnetite, biotite, and oxyhornblende indicate a modal range from olivine basalt to andesite. Major element analyses made on randomly collected samples, as well as on samples from systematically measured stratigraphic sections in localities of minimum erosion show ranges in Al₂O₃ (from 17.5 to 22.5 percent); SiO₂ (from 44.0 to 54.0 percent); MgO (from 3.47 to 8.20 percent) and CaO (from 7.19 to 11.90 percent). Na₂O/K₂O is always greater than 1.0. Ba⁺⁺ and Sr⁺⁺ abundances for some of the rocks are in agreement with those suggested, by workers in the field, for average basalt and andesite derived by melting of mantle or lower crust, but for many of the samples the values found are considerably higher. Although the presence of biotite in the earlier flows and oxyhornblende in the later ones along with the presence of much magnetite in all the rocks examined suggests that in part these rocks were derived by crystallization of a melt under conditions of high partial pressure of oxygen, the available trace element data indicates that contamination of the magma with crustal material was also a factor in their developmental history. The case for a parent magma, subsequently fractionally crystallized and contaminated in part, is strengthened by the occurrence of crystal cumulates and highly altered xenoliths in some of the flows.     

Petrology of filicudi,aeolian archipelago

Volcanic rocks on the island of Filicudi are typical of the cale-alkaline association of the Aeolian archipelago, and range in composition from basalt to high-K andesite. All specimens contain abundant phenocrystic plagioclase (cores of An_82–97, rims becoming progressively more sodic with increasing Differentiation Index), clinopyroxene, and magnetite; the most basic samples contain olivine, which is replaced by orthopyroxene at around D.I.=44. SiO₂ generally increases with time, and this in conjunction with the continuity in mineralogy suggests that the lavas are the differentiation products of a single batch of magma. Least-squares mixing calculations are consistent with a shallow fractional model, as is the variation in trace element abundances.     

Electrical conductivity of igneous rocks: Composition and temperature relations

The conductivity of four igneous rocks with, 49, 65, 77, and 84% SiO₂ was measured as a function of temperature in the interval from 20° to 1280°C; measurements were made in a vacuum of 10^?3 torr. No simple relationships were found between conductivity and SiO₂ content or versus major element groupings such as Na₂O=K₂O=CaO and TiO₂=Cr₂O₃=Al₂O₃=Fe₂O₃=FeO. An analytical expression was obtained between conductivity and the albite-quartz ratio, valid for temperatures between 300° and 1200°C. It was necessary to compute the CIPW norm in order to obtain the albite and quartz percentages. The onset of melting apparently occurred between 600° and 700°C. Petrography performed on two samples after cooling showed 70 and 85% partial melting. Three conduction regions were identified: 1) below 300°C, 2) between 300°C and 600°C, and 3) above 600°C. Different activation energies obtained for the heating and cooling intervals confirm that the sample undergoes textural changes in the heating-cooling cycle. Activation energy increments of 0.1 and 0.2 eV per decade of albite-quartz ratio were obtained.     

Volcanic rocks of the Witu Islands,Papua New Guinea: The origin of magmas above the deepest part of the New Britain Benioff zone

The Witu Islands are Quaternary volcanoes that overlie the deepest (about 300–580 km) part of the New Britain Benioff zone. The islands are about 100 km south of the transcurrent-divergent plate boundary that crosses the Bismarck Sea, and they surmount the southeastern end of the Willaumez-Manus Rise. The rocks are olivine- and quartz-normative tholeiitic basalts, low- and high-SiO₂ andesites, dacites, and rhyolites. Alkaline rocks that overlie the deep (greater than 300 km) parts of other Benioff zones have not been found in the Witu Islands. Compared to the Witu Islands rocks, those with similar SiO₂ contents from New Britain volcanoes that overlie progressively shallower parts of the Benioff zone to the south, are, for example, generally poorer in Na+K, Ti, and P, and higher in Ca and Al. There are similar progressive changes in trace-element abundances, but Zr and Nb contents are distinctly richer in Witu Islands rocks.⁸⁷Sr/⁸⁶Sr values range between 0.70311 and 0.7038, which are typical for rocks from New Britain as a whole and from other island arcs in the southwest Pacific. Two¹⁴³Nd/¹⁴⁴Nd values of 0.512211 and 0.512271, taken together with the Sr isotopic results, define a source region equivalent to those for oceanic-island basalts; there is no evidence for sea-water contamination of the sources. Perhaps the most striking feature of the Witu Islands rocks is their compositional diversity. Basalts range from olivine tholeiites similar to marginal-basin basalts from other areas, to quartz tholeiites similar in most respects to those typical of island arcs, and to incompatible-element-enriched tholeiites that are close to silica-undersaturation. Andesites on Unea Island have a strong island-arc signature, but the andesites, dacites, and rhyolite of Garove Island have some features that may be more in common with the silica-oversaturated rocks of oceanic areas. The mineralogy of Witu Islands basalts is characterised by phenocrysts of olivine (Fo_89-54), plagioclase (An_90-55) and Ca-augite. Cr-Al-rich spinels and aluminous magnetites are present as inclusions in some olivine phenocrysts. Groundmass fayalite, alkali feldspar, and dacitic to rhyolitic glasses high in K/Na are found in a few samples. In contrast to basalts from volcanoes above the shallower parts of the New Britain Benioff zone, those of the Witu Islands are characterised by rarity of low-Ca pyroxene, as phenocrysts or in the groundmass. Rocks richer in SiO₂ are characterised by the presence of orthopyroxene phenocrysts and lesser amounts of olivine. Hydrous minerals appear to be absent. Groundmass Fe-Ti oxides define crystallisation temperatures (about 800–1050°C) and oxygen fugacities (fO₂) corresponding to those of the Ni-NiO buffer, but up to two fO₂ log units above it. The suite as a whole is phenocryst-poor compared to most New Britain volcanic rocks. A significant degree of mantle heterogeneity is inferred by the chemical variability of the Witu Islands rocks. However, there are no compelling reasons in support of the interpretation that source heterogeneity is due to the effect of a slab-derived component. The cause of the heterogeneity is unclear, but may be due to mantle differentiation processes related to an anomalous tectonic setting.     

Chemistry and metal contents of magmatic gases: the new Tolbachik volcanoes case (Kamchatka)

The gaseous products of new Tolbachik volcanoes were studied during 1975 to 1977 throughout all eruptive stages and during the post eruptive activity. In investigations the northern break-out gases emitted during the eruption from the moving and consolidated lava flows there have been detected H₂O (the main component), H₂, HF, HCl, SO₂ and H₂S, CO₂, CO, NH₃, CH₄ and other hydrocarbons, NH₄Cl predominated in compositions of condensates and subtimates on lava flows and the most characteristic microcomponents were Zn, Cu, Pb, Sn, Ag and others. Sampling of gases and condensates at the southern break-out was conducted immediately from the flowing melt. In gases there have been detected H₂O (98 mol. %). HCl and H₂ (0.9 mol. % each) as well as HF, SO₂, H₂S, CO₂ and in small quantities O₂ and N₂, Gases reached the equilibrium state atT andP sampling and were characteristic of gas composition of the southern break-out magma. HCl, HF and H₂SO₄ were predominant during condensate and sublimate mineralization. The major raicrocomponents were represented by Pt, Sb, As, Zn, Cu, Pb, Ni, Co and others. Comparison of compositions of gases and of products of their reactions at the northern and at the southern break-outs allows us to assume the presence of the deeper magma source at the northern break-out and of shallow magma source at the southern break-out.     

A Statistical Framework for Calculating and Assessing Compositional Linear Trends Within Fault Zones: A Case Study of the NE Block of the Clark Segment,San Jacinto Fault,California, USA

Utilizing chemical data derived from the various fault zone architectural components of the Clark strand of the San Jacinto fault, southern California, USA, we apply for the first time non-central principal component analysis to calculate a compositional linear trend within molar A–CN–K space. In this procedure A–CN–K are calculated as the molar proportions of Al₂O₃ (A), CaO* + Na₂O (CN), and K₂O (K) in the sum of molar Al₂O₃, Na₂O, CaO*, and K₂O. CaO* is the molar CaO after correction for apatite. We then derive translational invariant chemical alteration intensity factors, t, for each architectural component through orthogonal projection of analyzed samples onto the compositional linear trend. The chemical alteration intensity factor t determines the relative change in composition compared to the original state (i.e., the composition of the altered wall rocks). It is dependent on the degree of intensity to which the process or processes responsible for the change in composition of each architectural component has been active. These processes include shearing, fragmentation, fluid flow, and generation of frictional heat. Non-central principal component analysis indicates that principal component 1 explains 99.7 % of the spread of A–CN–K data about the calculated compositional linear trend (i.e., the variance). The significance level for the overall one-way analysis of variance (ANOVA) is 0.0001. Such a result indicates that at least one significant difference across the group of means of t values is different at the 95 % confidence level. Following completion of the overall one-way ANOVA, the difference in means t test indicated that the mean of the t values for the fault core are different than the means obtained from the transition and damage zones. In contrast, at the 95 % confidence level, the means of the t values for the transition and damage zones are not statistically distinguishable. The results of XRD work completed during this study revealed that the <2 µm fraction is composed primarily of illite/smectite with ~15 % illite in the damage zone, of illite/smectite with ~30 % illite in the transition zone, and of discreet illite with very minor smectite in the fault core. These changes parallel the increasing values of the chemical alteration intensity factors (i.e., t). Based on the above results, it is speculated that when fault zones are derived from tonalitic wall rocks at depths of ~400 ± 100 m, the onset of the illite/smectite to illite conversion will occur when t values exceed 0.20 ± 0.12, the average chemical alteration intensity factor calculated for the transition zone. Under such conditions during repeated rupturing events, frictional heat is produced and acidic fluids with elevated temperatures (≥ ~125 °C) are flushed through the fault core. Over time, the combination of shearing, fragmentation, and frictionally elevated temperatures eventually overcomes the kinetic barrier for the illite/smectite to illite transition. Such settings and processes are unique to fault zones, and as a result, they represent an underappreciated setting for the development of illite from illite/smectite. The success of non-central principal component analysis in this environment offers the first statistically rigorous methodology for establishing the existence of compositional linear trends in fault zones. This method also derives quantifiable alteration intensity factors that could potentially be used to compare the intensity of alteration at different segments of a fault, as well as offer a foundation to interpret the potential driving forces for said alteration and differences therein.     

The quaternary caldera volcano emuruangogolak,kenya rift,and the petrology of a bimodal ferrobasalt-pantelleritic trachyte association

Emuruangogolak is a Quaternary basalitrachyte volcano situated in the Suguta graben of the northern Kenva rift, and probably erupted last early in this century. Following the construction of an early trachytic shield volcano, two episodes of caldera collapse occurred. each preceded by explosive pvroclastic activity. Post-calelera volcanism consisted of alternating phases of basalt and trachyte eruption. The basic lavas are high-Ti ferrobasalts of a mildly alkaline ‘transitional’ composition and the trachytes are peralkaline and oversaturated. A distinct compositional bimodality exists and no rocks in the range 49–59°. SiO, have been found. Major and trace element analyses suggest that the trachytes are genetically related to the basalts. Associations of almost identical lavas occur in Ethiopia. Pantelleria and the Azores but with the presence of intermediate terms Fractional crystallization is the mechanism currently preferred to account for the origin of the trachytes. The ‘Daly gap’ may be a consequence of a crystallization process which limits the volume of intermediate magma available at any time. In addition, the physical properties and spatial distribution of the different magmas probably discriminate against the cruption of lavas of intermediate composition.     

Petrogenesis and tectonic setting of the Queershan composite granitic pluton,eastern Tibetan Plateau: Constraints from geochronology,geochemistry and Hf isotope data

The Queershan composite granitic pluton is located in the north of the late Paleozoic Yidun arc collision-orogenic belt, eastern Tibetan Plateau. The main rock types are coarse-grained porphyritic alkalic-monzonite granite with minor fine-grained porphyritic monzogranite and granodiorite distributed in the eastern and southwestern regions. Here we report their zircon U-Pb ages and geo- chemical data. The intrusive contact relations indicate that granodiorite was formed earlier than the alkalic-monzonite granite(105.9±1.3 Ma) and monzogranite(102.6±1.1 Ma). These suggest that the Queershan composite granitic pluton was formed through three-stage magmatic events. The alkalic-monzonite granite(105.9±1.3 Ma) and monzogranite(102.6±1.1 Ma) are characterized by high SiO2(73.5%–77.7%), K2O+Na2O(6.9%–8.5%), Ga/Al ratios(2.6–3.4) and low Al2O3(11.8%–14.5%), CaO(0.25%–1.5%), MgO(0.18%–0.69%), negative Ba, Sr and Eu anomalies, showing A-type granite affinities. The granodiorite exhibits lower SiO2, P2O5 and K2O+Na2O contents, but higher Al2O3, CaO and MgO contents than alkalic-monzonite granite and monzogranite, showing I-type granite affinity. 176Hf/177 Hf ratios of the alkalic-monzonite granite and the monzogranite are 0.282692–0.282749 and 0.282685–0.282765, respectively, and with similar ?Hf(t) values(?0.56 to 1.43 and ?0.87 to 1.90 respectively). They also present similar TDM2 model ages(1.04–1.22 and 1.07–1.2 Ga respectively), indicating they may be sourced from a similar rock source, mostly like Kangding Complex. The homogeneity of the Hf isotopic compositions and the absence of the MMEs demonstrate that little depleted mantle materials have contributed to the source. We propose that the Mesoproterozoic crust materials of the Yangtze Craton exist beneath the Yidun arc terrane and support it was a dismembered part of the Yangtze Craton. The A-type granites of Queershan composite granitic pluton are most probably related to the closure of the Bangong-Nujiang Tethys ocean.     

Geochemistry of the volcanics of central Mexico

The Tertiary and Recent volcanics of Mexico occur in two provinces. The Cordillera Province is made up of about 1700 m of ignimbrite sheets overlain and intercalated in the upper part by olivine basalt and basaltic andesite. The Rio Lerma Province extends transversely across Mexico and in the Valley of Mexico the lavas consist mainly of andesite and dacite, 68 % of those analysed having 62 | 4.7 % SiO₂. A total of 108 chemical analyses were made for the major elements, 90 of these including determinations of Cr, Ni, Cu, Zn, Rb, Sr, Ba, Th and Pb for two areas, the Valley of Mexico in the Rio Lerma Province and the Guadalajara region which lies at the intersection of the two provinces. Computer constructions of normative components in the basalt tetrahedron and other projections support an origin of partial melting of tholeiitic to pyrolitic material for the production of andesite. The Guadalajara lavas have consistently higher K/SiO₂ and K/Rb ratios and lower Mg/SiO₂ ratio than the Valley of Mexico rocks suggesting generation at greater depth.     

Petrology of the hilina formation,Kilauea volcano,Hawaii

The Hilina Formation comprises the oldest sequence of lava flows and tuffs exposed on Kilauea Volcano. These rocks are only exposed in kipukas in younger Puna Formation lavas along cliffs on the south flank of Kilauea Volcano. Locally, tuffs and flows of the Pahala Formation separate the underlying Hilina Formation rocks rom the overlying Puna Formation rocks. Charcoal collected from the base of the Pahala Formation yielded a C¹⁴ age of 22.800±340 years B.P. which defines a minimum age for the Hilina Formation. Hilina Formation lavas crop out over a wide region and probably originated from the summit area and from both rift zones. The Hilina Formation contains both olivine-controlled and differentiated lavas (using the terminology ofWright, 1971). The olivine-controlled lavas of the Hilina Formation are distinguishable mineralogically and geochemically from younger olivine-controlled Kilauea lavas. The younger lavas generally contain discrete low-calcium pyroxene grains. greater glass contents, higher K₂O/P₂O₅ ratios and lower total iron contents. Similar geochemical trends prevail for Manuna Loa lavas, and may typify the early lavas of Hawaiian shield volcanoes. Despite these similarities, the Hilina Formation (and all Kilauea) lavas have higher TiO₂ and CaO, and lower SiO₂ and Al₂O₃ contents than Mauna Loa Lavas. These differences have existed for over 30,000 years. Therefore, it is unlikely that the older lavas of Kilauea are compositionally similar to recent Mauna Loa lavas as was previously suggested. K₂O, TiO₂, Na₂ and Zr contents of lavas from a stratigraphic sequence of Hilina Formation lavas are variable. These variations may be utilized to subdivide the sequence into geochemical groups. These groups are not magma batches. Rather, they represent lavas from batches whose compositions may have been modified by crystal fractionation and magma mixing.