Observations on the boundary between zeolite facies and prehnite-pumpellyite facies

Using graphical analysis of the system CaO-Al₂O₃-SiO₂-H₂O-CO₂, this paper derives a topology relating the minerals calcite, laumontite, wairakite, prehnite, quartz, and zoisite. Simple thermodynamic reasoning allows this system to be applied to natural rocks and indicates that the first appearance of the assemblage epidote-chlorite-quartz (±albite) should mark the upper boundary of zeolite facies. This assemblage forms at the expense of laumontite+prehnite, laumontite+calcite, or laumontite+pumpellyite, with wairakite likely to replace laumontite as the stable zeolite at low pressures. In natural systems this proposed facies boundary is multivariant and, hence, it is likely to be strongly sensitive to compositional variables. For example, Na-bearing wairakite will be more stable than pure Ca-wairakite and increasing abundance of Fe³⁺ will tend to stabilize epidote+quartz at the expense of the zeolites. Because of this, monitoring the composition of minerals such as epidote, prehnite, or wairakite from lowvariance assemblages may provide a more-sensitive indicator of metamorphic grade than the presence or absence of any particular mineral assemblage.     

A new petrogenetic grid for low-grade metabasites

Abstract We have used internally-consistent thermodynamic data to present calculated phase equilibria for the system Na₂O-CaO-MgO-Al₂O₃-SiO₂-H₂O (NCMASH), in the range 0–500° C and 0.1–10 kbar, involving the phases anorthite, glaucophane, grossular, heulandite, jadeite, laumontite, lawsonite, paragonite, prehnite, pumpellyite, stilbite, tremolite, wairakite, zoisite with excess albite, clinochlore, quartz and pure water. Average activity terms derived from published mineral chemical data were included for clinochlore, glaucophane, prehnite, pumpellyite, tremolite, and zoisite. The new petrogenetic grid delineates stability fields and parageneses of common index minerals in zeolite, prehniteactinolite, prehnite-pumpellyite, pumpellyite-actinolite, blueschist and greenschist facies metabasites. The stability fields of mineral assemblages containing prehnite, pumpellyite, epidote, actinolite (+ albite + chlorite + quartz) were analysed in some detail, using activity data calculated from five specific samples. For example, the prehnite-actinolite facies covers a P-T field ranging from about 220 to 320° C at pressures below 4.5 kbar. The transition from the prehnite-actinolite and pumpellyite-actinolite to greenschist facies occurs at about 250–300° C at 1–3 kbar and at about 250–350° C at 3–8 kbar. P-T fields of individual facies overlap considerably due to variations in chemical composition.     

克拉玛依油区沸石类矿物特征及其与油气的关系

克拉玛依油区储层中共发现6种沸石和一种与沸石演化有关的钠长石。本文通过沸石矿物特征及分布规律的研究认为;沸石及沸石的组合在纵向上存在着一定的分带性,与埋藏成岩关系极为密切。方沸石和方沸石十片沸石带为早成岩期B阶段形成;片沸石十浊沸石带主要为晚成岩期A阶段形成;浊沸石+钠长石带为晚成岩期B—c阶段形成。方沸石的钠长石化和方沸石溶蚀对储层贡献较大。另外对沸石分带中的一些重叠现象等进行了初步探讨。     

Zeolite and prehnite-pumpellyite facies in south central Puerto Rico

The intermediate lavas and pyroclastic rocks of south central Puerto Rico have been subjected to about four kilometers of burial. Despite shallow burial the mineralogy of these rocks has systematically readjusted. The degree of metamorphism is proportional to permeability; secondary phases appear in greater quantities in porous pyroclastics. In lavas, plagioclase and olivine phenoerysts contain a progressive sequence of alteration phases reflecting temperature and pressure conditions during alteration. The generalized sequence of appearance of secondary phases from low to high rank is as follows: 1. analcime, celadonite, chlorite, and sericite; 2. laumontite and albite; 3. prehnite; 4. pumpellyite; 5. epidote; 6. actinolite. Assemblages containing analcime, heulandite, celadonite, and laumontite belong to the zeolite facies. Remaining assemblages belong to the prehnite-pumpellyite facies.During alteration two major thresholds were crossed. First, calcium-aluminum silicates formed from materials released by decomposition of calcium feldspar. Second, clinopyroxene was decomposed in a process that added considerable mafic material to the reacting system, and made bulk rock compositions approximately equivalent to the composition of the reacting system. Comparison with other regions of similar metamorphic rank and composition indicates that zonation of such sequences on the basis of individual mineral occurrences, especially epidote, is justified only for local regions where the behavior of volatiles was uniform.Based on part of a dissertation (Jolly, 1969) presented to the faculty of the Department of Geology, State University of New York at Binghamton.     

Zeolites in volcanic-igneous hydrothermal systems: a case study of Pauzhetka geothermal field (Kamchatka) and Oligocene Smrekovec volcanic complex (Slovenia)

Production from geothermal reservoirs in volcanic-igneous hydrothermal systems may be disturbed owing to the formation of authigenic minerals that reduce primary porosity and infill fissure systems. Crystallization may be induced by natural processes or human activity related to the reservoir exploitation. In volcanic and volcaniclastic rocks, zeolites and related authigenic silicate minerals commonly develop. Two selected study sites—Pauzhetka geothermal field in Russia and Smrekovec volcanic complex in Slovenia are characterized by extensive development of progressive stage medium- and low-temperature propylitization and zeolitization with similar mineral assemblages that reduced original reservoir rock porosity and permeability. Retrograde and overprinting reactions of argillitization commonly enhance porosity and permeability of rocks, but some other reactions, like from prehnite to laumontite, from laumontite to heulandite, and from laumontite to analcime, encountered in the Smrekovec volcanic complex reduced it appreciably. Retrograde reactions recognized in the study sites were not induced by the temperature drop only, but were accompanied by the change in chemical composition of reacting fluids. Chemical composition of interstitial waters produced from exploitation wells in the Pauzhetka geothermal field indicate that propylitic and zeolite facies alteration is related to Na–Cl, slightly alkaline waters, while argillitization involved acidic thermal waters with more complex ion composition.     

Stilbite-laumontite equilibrium

The reaction stilbite=laumontite+3 quartz+3 H₂O was experimentally studied using conventional hydrothermal techniques employing mineral mixtures consisting of reactants and products in 91 and 19 ratios. Equilibrium was demonstrated; the univariant curve passes through about 170° C and 2000 bars, 185°±10° C and 3000 bars, about 185° C and 4000 bars, and 183°±10° C at 5000 bars P _fluid. These results combined with published equilibria for analcime, laumontite, wairakite and prehnite permit delineation of the P-T conditions for the zeolite and prehnite-pumpellyite facies metamorphism in the Tanzawa Mountains, Japan.     

酸性岩的变质相

在沸石相变质条件下,花岗岩里浊沸石交代了斜长石和石英,在酸性火山岩里产生明矾石、埃洛石或高岭石。经受绿纤石-葡萄石相变质的花岗岩,其中黑云母变为钙铝榴石、帘石、绿纤石和葡萄石集合体,同时斜长石发生绢云母化。绿片岩相内酸性岩的浅色矿物有石英、微斜长石、钠长石和绿帘石,暗色矿物有绿泥石和黑云母。在角闪岩相变质的酸性岩中,开始出现中、基性斜长石,其中暗色矿物黑云母的镁铁比值要大于角闪石的镁铁比值。经受麻粒岩相变质后,紫苏花岗岩的矿物组成没有变化,但有铀、钍和钾的迁出。     

Mineral assemblages and phase equilibria of metabasites from the prehnite–pumpellyite to amphibolite facies,with the Flin Flon Greenstone Belt (Manitoba) as a type example

An exceptionally well-exposed part of the Flin Flon Greenstone Belt (Manitoba/Saskatchewan) is used to characterize the mineral assemblage evolution associated with prehnite–pumpellyite through amphibolite facies metamorphism of basalts. Data from these rocks are combined with a large literature data set to assess the ability of current thermodynamic models to reproduce natural patterns, evaluate the use of metabasic rocks at these grades to estimate pressure–temperature (P–T) conditions of metamorphism, and to comment on the metamorphic devolatilization that occurs. At Flin Flon, five major isograds (actinolite-in, prehnite- and pumpellyite-out, hornblende-in, oligoclase-in, and actinolite-out) collectively represent passage from prehnite–pumpellyite to lower amphibolite facies conditions. The evolution in mineral assemblages occurs in two narrow (~1,000 m) zones: the prehnite–pumpellyite to greenschist facies (PP-GS) transition and greenschist to amphibolite facies (GS-AM) transition. Across the GS-AM transition, significant increases in the hornblende and oligoclase proportions occur at the expense of actinolite, albite, chlorite, and titanite, whereas there is little change in the proportions of epidote. The majority of this mineral transformation occurs above the oligoclase-in isograd within the hornblende–actinolite–oligoclase zone. Comparison with thermodynamic modelling results suggests data set 5 (DS5) of Holland and Powell (1998, Journal of Metamorphic Geology, 16 (3):309–343) and associated activity–composition (a–x) models is generally successful in reproducing natural observations, whereas data set 6 (DS6) (Holland & Powell, 2011, Journal of Metamorphic Geology, 29 (3):333–383) and associated a–x models fail to reproduce the observed mineral isograds and compositions. When the data from Flin Flon are combined with data from the literature, two main pressure-sensitive facies series for metabasites are revealed, based on prograde passage below or above a hornblende–albite bathograd at ~3.3 kbar: a low-pressure ‘actinolite–oligoclase type’ facies series, characterized by the appearance of oligoclase before hornblende, and a moderate- to high-pressure ‘hornblende–albite type’ facies series, characterized by the appearance of hornblende before oligoclase. Concerning the PP-GS transition, the mineral assemblage evolution in Flin Flon suggests it occurs over a small zone (<1,000 m), in which assemblages containing true transitional assemblages (prehnite and/or pumpellyite coexisting with actinolite) are rare. This contrasts with thermodynamic modelling, using either DS5 or DS6, which predicts a wide PP-GS transition involving the progressive appearance of epidote and actinolite and disappearance of pumpellyite and prehnite. Patterns of mineral assemblages and thermodynamic modelling suggest a useful bathograd (‘CHEPPAQ bathograd’), separating prehnite–pumpellyite-bearing assemblages at low pressures and pumpellyite–actinolite-bearing assemblages at higher pressures, occurs at ~2.3 to 2.6 kbar. Observations from the Flin Flon sequence suggests devolatilization across the GS-AM transition (average: ~1.8 wt% H₂O) occurs over a very narrow interval within the actinolite–hornblende–oligoclase zone, associated with the loss of >75% of the total chlorite. By contrast, modelling of the GS-AM transition zone predicts more progressive dehydration of ~2 wt% H₂O over a >50°C interval. Observations from the field suggest devolatilization across the PP-GS transition occurs over a very narrow interval given the rarity of transitional assemblages. Modelling suggests fluid release of 1.0–1.4 wt% resulting from prehnite breakdown over a ~10°C interval. This fluid may not be entirely lost from the rock package due to involvement in the hydration of igneous mineralogy across the PP-GS transition as observed in the Flin Flon sequence.     

Characteristics of Triassic epithermal Au mineralization at the Q prospect,Chatree mining area,Central Thailand

The Chatree deposit is located in the Loei‐Phetchabun‐Nakhon Nayok volcanic belt that extends from Laos in the north through central and eastern Thailand into Cambodia. Gold‐bearing quartz veins at the Q prospect of the Chatree deposit are hosted within polymictic andesitic breccia and volcanic sedimentary breccia. The orebodies of the Chatree deposit consist of veins, veinlets and stockwork. Gold‐bearing quartz veins are composed mainly of quartz, calcite and illite with small amounts of adularia, chlorite and sulfide minerals. The gold‐bearing quartz veins were divided into five stages based on the cross‐cutting relationship and mineral assemblage. Intense gold mineralization occurred in Stages I and IV. The mineral assemblage of Stages I and IV is characterized by quartz–calcite–illite–laumontite–adularia–chlorite–sulfide minerals and electrum. Quartz textures of Stages I and IV are also characterized by microcrystalline and flamboyant textures, respectively. Coexistence of laumontite, illite and chlorite in the gold‐bearing quartz vein of Stage IV suggests that the gold‐bearing quartz veins were formed at approximately 200°C. The flamboyant and brecciated textures of the gold‐bearing quartz vein of Stage IV suggest that gold precipitated with silica minerals from a hydrothermal solution that was supersaturated by boiling. The δ¹⁸O values of quartz in Stages I to V range from +10.4 to +11.6‰ except for the δ¹⁸O value of quartz in Stage IV (+15.0‰). The increase in δ¹⁸O values of quartz at Stage IV is explained by boiling. P_H2O is estimated to be 16 bars at 200°C. The f_CO2 value is estimated to be 1 bar based on the presence of calcite in the mineral assemblage of Stage IV. The total pressure of the hydrothermal solution is approximately 20 bars at 200°C, suggesting that the gold‐bearing quartz veins of the Q prospect formed about 200 m below the paleosurface.     

Isotope systematics of secondary minerals from the Prospect Intrusion,New South Wales

The differentiated Mesozoic alkali dolerite Prospect Intrusion contains a wide range of secondary minerals, including carbonates (primarily calcite), laumontite, prehnite and heulandite, whose stability relationships imply a formation temperature of <200°C. The δ¹⁸O data for carbonates define a higher temperature (160 – 195°C) suite, and a lower temperature (51 – 73°C) suite. The δ¹³C, δ¹⁸O and ⁸⁷Sr/⁸⁶Sr isotope systematics for these carbonates suggest derivation of the higher temperature group from magmatic fluids, whereas the other group had a major meteoric component that probably originated from porewater in the country rock. Source fluids for prehnite were meteoric rather than magmatic in origin based on their δD and δ¹⁸O ratios. Early in the intrusion's emplacement, CO₂-rich hydrothermal fluids formed a carbonate rind sealing the upper part of the hydrothermal system and produced the higher temperature carbonates (calcite) and laumontite. Later, cooler fluids with a meteoric component infiltrated vesicles and fractures, depositing the lower temperature carbonates (calcite, aragonite), heulandite and prehnite.     

Textural evolution and metamorphism of pillow basalts from the Franciscan Complex,western Marin County,California

Petrogenesis of Franciscan pillow basalts from the Franciscan Complex of western Marin County California entails both dynamic crystallization of tholeiitic magma and subsequent low-temperature metamorphism. Brittle deformation during tectonic emplacement of pillow basalts into a chert greywacke terrain is manifested by the shearing of interpillow matrix and polishing of pillow rims, but the igneous textures within pillows are well preserved.The cooling history of pillow basalts can be understood through analysis of morphologic variations of primary olivine and plagioclase from rim to core of the pillow. Crystal sizes and plagioclase dendrite spacings are consisted with a cooling rate which generally decreases inward. Some pillows show a marked asymmetry in plagioclase and olivine morphology suggesting lower cooling rates caused by asymmetric cooling of the pillows. Olivine morphologies, primarily hopper and chain forms, are consistent with cooling rates of 2–10 °C/h for pillow cores and 50–75 °C/h for pillow rims.Low temperature hydrothermal alteration has produced secondary minerals indicative of zeolite facies conditions. Pillow matrix is either chloritic or zeolitic (in part laumontized). Pillow rims display incomplete replacement of calcic palagonite by pumpellyite (Fe₂O₃=9–21 wt%), prehnite (Fe₂O₃=5–7 wt%), sphene and quartz. Metamorphism of pillow interiors, manifested by: (1) veins of quartz, pumpellyite, calcite, or harmotome (BaO=15 wt%); (2) amygdules containing analcime, chlorite or quartz; and (3) replacement of olivine by pumpellyite or smectite/illite, of plagioclase by albite (An3)+sericite, and of glassy groundmass by fine-grained chlorite. Primary augite (Wo3₃₉En₁₃Fs₄₈) was not altered. The described paragenesis may be attributed to oceanfloor and/or Franciscan-type metamorphism.     

A Petrographic and Mineralogical Study of Volcanic Rocks from the Mayaxueshan Area, North Qilian Fold Belt, NW China

The Ordovician volcanic rocks in the Mayaxueshan area have been pervasively altered or metamorphosed and contain abundant secondary minerals such as albite, chlorite, epidote, prehnite, pumpellyite, actinolite, titanite, quartz, and/or calcite. They were denoted as spilites or spilitic rocks in terms of their petrographic features and mineral assemblages. The metamorphic grades of the volcanic rocks are equivalent to that of the intercalated metaclastic rocks. This indicates that both the spilitic volcanic rocks and metaclastic rocks in the Mayaxueshan area have formed as a result of Caledonian regional metamorphism. We suggest that the previously denoted spilitic rocks or altered volcanic rocks should be re-denoted as metabasalts or metabasaltic rocks. The metamorphic grade of the volcanic rocks increases with their age: prehnite-pumpellyite facies for the upper part of the Middle Ordovician volcanic rocks, prehnite-pumpeilyite to lower greenschist facies for the lower part of the Middle Ordovician vol     

Cold subduction of the Neotethys: the metamorphic record from finely banded lawsonite and epidote blueschists and associated metabasalts of the Nagaland Ophiolite Complex,India

In this study, we have deduced the thermal history of the subducting Neotethys from its eastern margin, using a suite of partially hydrated metabasalts from a segment of the Nagaland Ophiolite Complex (NOC), India. Located along the eastern extension of the Indus‐Tsangpo suture zone (ITSZ), the N–S‐trending NOC lies between the Indian and Burmese plates. The metabasalts, encased within a serpentinitic mélange, preserve a tectonically disturbed metamorphic sequence, which from west to east is greenschist (GS), pumpellyite–diopside (PD) and blueschist (BS) facies. Metabasalts in all the three metamorphic facies record prograde metamorphic overprints directly on primary igneous textures and igneous augite. In the BS facies unit, the metabasalts interbedded with marble show centimetre‐ to metre‐scale interlayering of lawsonite blueschist (LBS) and epidote blueschist (EBS). Prograde HP/LT metamorphism stabilized lawsonite + omphacite (X_Jd = 0.50–0.56 to 0.26–0.37) + jadeite (X_Jd = 0.67–0.79) + augite + ferroglaucophane + high‐Si phengite (Si = 3.6–3.65 atoms per formula unit, a.p.f.u.) + chlorite + titanite + quartz in LBS and lawsonite + glaucophane/ferroglaucophane ± epidote ± omphacite (X_Jd = 0.34) + chlorite + phengite (Si = 3.5 a.p.f.u.) + titanite + quartz in EBS at the metamorphic peak. Retrograde alteration, which was pervasive in the EBS, produced a sequence of mineral assemblages from omphacite and lawsonite‐absent, epidote + glaucophane/ferroglaucophane + chlorite + phengite + titanite + quartz through albite + chlorite + glaucophane to lawsonite + albite + high‐Si phengite (Si = 3.6–3.7 a.p.f.u.) + glaucophane + epidote + quartz. In the PD facies metabasalts, the peak mineral assemblage, pumpellyite + chlorite + titanite + phengitic white mica (Si = 3.4–3.5 a.p.f.u.) + diopside appeared in the basaltic groundmass from reacting titaniferous augite and low‐Si phengite, with prehnite additionally producing pumpellyite in early vein domains. In the GS facies metabasalts, incomplete hydration of augite produced albite + epidote + actinolite + chlorite + titanite + phengite + augite mineral assemblage. Based on calculated T–M(H₂O), T–M(O₂) (where M represents oxide mol.%) and P–T pseudosections, peak P–T conditions of LBS are estimated at ~11.5 kbar and ~340 °C, EBS at ~10 kbar, 325 °C and PD facies at ~6 kbar, 335 °C. Reconstructed metamorphic reaction pathways integrated with the results of P–T pseudosection modelling define a near‐complete, hairpin, clockwise P–T loop for the BS and a prograde P–T path with a steep dP/dT for the PD facies rocks. Apparent low thermal gradient of 8 °C km^?1 corresponding to a maximum burial depth of 40 km and the hairpin P–T trajectory together suggest a cold and mature stage of an intra‐oceanic subduction zone setting for the Nagaland blueschists. The metamorphic constraints established above when combined with petrological findings from the ophiolitic massifs along the whole ITSZ suggest that intra‐oceanic subduction systems within the Neotethys between India and the Lhasa terrane/the Karakoram microcontinent were also active towards east between Indian and Burmese plates.     

Zeolite and clay-carbonate assemblages in the Blairmore Group (Cretaceous) southern Alberta Foothills,Canada

Zeolites, calcite, quartz, kaolinite, chlorite and other authigenic minerals occur in the non-marine sandstones of the Lower Cretaceous Blairmore Group of the southern Alberta Foothills, Canada. Zeolites are restricted to plagioclase-rich sandstones and do not occur with kaolinite. Laumontite and barian-strontian heulandite (containing up to 6.9 weight percent BaO and 4.1 weight percent SrO) generally occur as pore fillings, but laumontite also occurs within albitized plagioclase. About 80 percent of plagioclase grains examined by electron microprobe are partly to completely albitized. A structural-stratigraphic reconstruction of the areas sampled indicate maximum burial depths, including tectonic thickening, in the range 4.7 to 7.8 Km, with P load ～1 to ～2 Kb, respectively. A comparison of mineral assemblages in Blairmore rocks with published experimental data suggest T did not exceed ～250°–280°C, depending on the load pressure. If P _H2O∶P load, the presence of laumontite and albite suggest minimum T on the order of 150°–180°C. The lack of lawsonite suggests P-load <3Kb, which is compatible with structural-stratigraphic data. The occurrence of the alternative assemblages calcite-kaolinite-quartz and laumontite implies gradients in f _CO2/f _HO2. Assemblages containing laumontite presumably equilibrated with fluids having X _CO2a Mg⁺⁺/a (H⁺)². X-ray diffraction studies on disordered graphitic material indicate a comparable degree of graphitization between Blairmore graphitic material and that found in zeolite facies assemblages elsewhere. If log f _O2 were at least as low as that defined by quartz-magnetite-fayalite buffer, disordered graphite could not have equilibrated with fluids of the same composition as those equilibrated with laumontite or kaolinite.     

Mass transfer and porosity evolution during low temperature water–rock interaction in gneisses of the simano nappe: Arvigo,Val Calanca,Swiss Alps

Late Alpine fissures and fractures in amphibolite-facies basement gneisses at Arvigo (Val Calanca, Swiss Alps) show distinct cm-sized reaction selvages parallel to the fracture walls that composed of subgreenschist facies assemblages produced by the interaction of water present in the fracture porosity with the old high-grade gneiss assemblages. The process of selvage or reaction-vein formation occurred in the brittle deformation regime and at temperatures characteristic of, first the prehnite-pumpellyite facies and then later of the zeolite facies. The vein formation occurred during uplift and cooling at very late stages of the Alpine orogeny. The reaction veins are composed of a selvage of altered gneiss on both sides of the central fracture and a central zone with fissure minerals that have been growing in the open fracture pore space. The central zone of the Arvigo veins contains an early assemblage with epidote, prehnite and chlorite and a late succession sequence of various species of zeolite. The veins of the Arvigo quarry are convincing evidence that fracture fluids in gneiss and granite have the potential to precipitate Ca–zeolite. This is an important find because many fluids recovered from deep continental drill holes and from geothermal energy exploration are found to be oversaturated in respect to a number of Ca–zeolite species. Vein formation during late uplift and cooling of the Alps occurred at continuously decreasing T and at hydrostatic pressure: (1) coexisting prehnite/epidote records temperatures of 330–380°C, (2) chlorite formation at temperature of 333 ± 32°C and (3) formation of zeolites <250°C. In the selvages the prime reaction is the replacement of plagioclase by albite along a sharp reaction front that separates the selvage from unaltered gneiss. In addition to albitisation, chloritisation of biotite is the second important reaction in the alteration process. The reactions release components for the formation of Ca–Al silicates. The water–rock interaction is associated with a depletion of Al, Si, Ca, Fe and K in the altered wall rock. The overall reaction is associated with an increase in porosity of up to 14.2 ± 2.2% in the selvage zone (altered wall rock), caused by the volume decrease during albitisation and the removal of biotite. The propagation of the sharp reaction front through the gneiss matrix occurred via a dissolution-reprecipitation mechanism. Zeolite formation is tied to the plagioclase alteration reaction in the rock matrix, which releases components for zeolite formation to a CO₂-poor aqueous liquid.     

Geological, mineralogical and geochemical characteristics of zeolite deposits associated with borates in the Bigadiç, Emet and Kirka Neogene lacustrine basins, western Turkey

The Bigadiç, Emet and Kirka lacustrine basins of western Turkey may be considered as Tibet-type graben structures that were developed during the Miocene within the Izmir-Ankara suture zone complex. The volcanic-sedimentary successions of these basins are made up of mudstone, carbonate (limestone and dolomite) and detrital rocks, and also of crystal or vitric tuffs about 135 to 200 m thick. The Degirmenli (Bigadiç), Emirler (Bigadiç) Köpenez (Emet) and Karaören (Kirka) tuffs constituting the zeolite deposits are situated beneath four borate deposits (colemanite, ulexite, borax). The most abundant diagenetic silicate minerals are K- and Ca-clinoptilolites in the zeolite deposits, and Li-rich trioctahedral smectites (stevensite, saponite and hectorite) and K-feldspar in the borate deposits. In the Degirmenli, Emirler. Köpenez and Karaören deposits, the following diagenetic faciès were developed from rhyolitic glasses rich in K and poor in Na: (glass + smectite), (K-clinoptilolite + opal-CT), (Caclinoptilolite + K-feldspar ± analcime ± quartz) and (K-feldspar+analcime+quartz). K-feldspar which is also rarely associated with phillipsite (Karaören) and heulandite (Degirmenli and Karaören), succeeds clinoptilolite and precedes analcime in these diagenetic facies where dioctahedral smectites, opal-CT and quartz are the latest minerals. No diagenetic transformations exist between clinoptilolite, K-feldspar and analcime that were formed directly from glass. The lateral facies distributions resulted from the differences in salinity and pH of pore water trapped during deposition of the tuffs, but vertical distributions in vitric tuffs seem to have been controlled by the glass/liquid ratio of the reacting system and the permeability or diffusion rate of alkali elements. The Bigadiç, Emet and Kirka zeolite deposits which were formed in saline basins rich in Ca and Mg ions, show similar chemical changes, i.e. loss of alkalis and gain in alkaline-earth elements that have taken place during the diagenetic transformation of rhyolitic glasses to dioctahedral smectites or clinoptilolite. The absence of sodic zeolites such as mordenite, erionite, chabazite and silica-rich phillipsite is mainly due to the very high K/Na ratio of the starting materials rather than initial alkaline conditions or high Na content in lake waters.     

Jadeitites, albitites and related rocks from the Motagua Fault Zone, Guatemala

Jadeitites from Guatemala are found as weathered blocks in tectonized serpentinite in a 15-km zone north of the Motagua Fault Zone. Rock types found with jadeitite include albitites, albite-mica rocks, omphacite/taramitic amphibole-bearing metabasites, chlorite-actinolite schists, talc-carbonate rocks and antigorite schists. In addition to the predominant jadeitic (Jd₉₃_₁₀₀) pyroxene, common phases in jadeitite include micas (paragonite and/or phengite ± rarer phlogopite), omphacite, albite, titanite /Pm zircon, apatite and graphite. Conditions of jadeitite formation are 100-400d? C, 5-11 kbar with 0.0 > log₁₀a_sio2≥= 0.7. Fluid inclusions, coarse textures, vein structures, and rhythmic zoning of pyroxene indicate an aqueuos fluid was involved. Jadeitites are either (1) metasomatic modifications of former felsic-to-pelitic inclusions that have undergone silica depletion plus efficient soda exchange and enrichment, or (2) solution precipitations derived from such a source. The close spatial relationship of faults and shear zones, serpentinites, and jadeitites suggests jadeitites form in a relatively high-P/T setting with substantial flow of sodic fluid in a tectonized zone. Most Guatemalan jadeitites are extensively altered to analcime, albite, taramitic amphibole, (clino)zoisite ± nepheline and preiswerkite. This alteration reflects depressurization /Pm heating to below the jadeite + fluid = analcime reaction at high a_Na. With progressive alteration, analcime and nepheline are replaced by albite; the increase in silica content may result from fluid flowing up a tectonized zone reaching saturation with an albite assemblage. Albitite phases, albite, actinolite, zoisite, /Pm chlorite, phengite, K-feldspar and quartz, record conditions of c. 3-8 kbar at T < 400d? C, indicating a clockwise P-T trajectory of the blocks. Barium aluminosilicates—banalsite, celsian, cymrite and hyalophane—are common minor late-stage phases in jadeitites and albite-rich rocks. Barian phengite is common in albite-mica rocks.     

三塘湖盆地条湖组含沉积有机质凝灰岩致密储层特征

含沉积有机质凝灰岩是三塘湖盆地一种特殊类型的致密储层,对这套含沉积有机质凝灰岩致密储层的研究将为提高我们对非常规致密储层的认识提供一个很好的机会。文中通过凝灰岩样品岩石矿物组成、薄片、扫描电镜、石英结晶度和物性等的分析,阐述了三塘湖盆地二叠系条湖组含沉积有机质凝灰岩致密储层的特征。结果表明：条湖组凝灰岩致密储层的岩石类型主要有玻屑凝灰岩和晶屑玻屑凝灰岩,凝灰岩中最主要的矿物是石英,平均含量可以达到50%以上。凝灰岩致密储层的储集空间类型可以分为脱玻化作用形成的矿物粒间孔,溶蚀作用形成的粒内孔、无机矿物粒内孔和黏土矿物粒内孔,有机质孔以及裂缝。凝灰岩储层的物性具有高孔低渗的特点,孔隙度主要分布在10%~25%,空气渗透率主要分布在(0.01~0.5)×10-3 μm2,凝灰岩火山玻璃质的脱玻化作用是导致凝灰岩储层高孔低渗的主要因素,脱玻化形成的粒间孔体积小但数量巨大造成了凝灰岩总孔隙度较高,孔隙喉道半径极小又导致渗透率很低。凝灰岩储层物性主要受原始火山灰的组分以及脱玻化程度的控制,玻屑凝灰岩比晶屑玻屑凝灰岩储层物性好,脱玻化程度越高储层物性越好,而脱玻化程度主要受凝灰岩的埋深(温度)、有机质(有机酸)含量等因素控制。     

中国东部中生代火山岩中沸石岩的地质特征和成因

天然沸石是岩石圈上部分布最广的硅酸盐矿物之一,它普遍地见于各种火山岩和火山-沉积岩中。沸石不仅在岩浆期后热液阶段生成,而且在沉积-成岩作用阶段、表生作用(风化)阶段、低级变质阶段都可以生成。由于沸石对周围的物理化学条件和热、动力变质作用反应灵敏,因此,它是了解地质体形成时的地质环境及其变化的良好的指示矿物。本文概述了我国东部中生代火山岩中沸石岩的分布、时代、产出的地层岩性剖面、原岩类型、矿物组合及其生成顺序,并探讨了它的形成条件和成因类型,其中主要涉及具有工业意义的斜发沸石岩和丝光沸石岩。     

Pumpellyite–actinolite facies of the Sanbagawa metamorphism

The pumpellyite–actinolite facies proposed by Hashimoto is defined by the common occurrence of the pumpellyite–actinolite assemblage in basic schists. It can help characterize the paragenesis of basic and intermediate bulk compositions, which are common constituents of various low-grade metamorphic areas. The dataset of mutually consistent thermodynamic properties of minerals gives a positive slope for the boundary between the pumpellyite–actinolite and prehnite–pumpellyite facies in P–T space. In the Sanbagawa belt in Japan, the mineral parageneses of hematite-bearing and -free basic schists, as well as pelitic schists have been well documented. The higher temperature limit of this facies is defined by the disappearance of the pumpellyite+epidote+actinolite+chlorite assemblage in hematite-free basic schists with X_Fe3+ of epidote around 0.20–0.25 and the appearance of epidote+actinolite+chlorite assemblage with X^Ep_Fe3+≤0.20. In hematite-bearing basic schists, there is a continuous change of paragenesis to higher grade, epidote–glaucophane or epidote–blueschist facies. In pelitic schists, the albite+lawsonite+chlorite assemblage does occur but only rarely, and its assemblage cannot be used to determine the regional thermal structure. The lower temperature equivalence of the pumpellyite–actinolite assemblage is not observed in the field. The Mikabu Greenstone complex and the northern margin of the Chichibu complex, which are located to the south of the Sanbagawa belt, are characterized by clinopyroxene+chlorite or lawsonite+actinolite assemblages, which are lower temperature assemblages than the pumpellyite+actinolite assemblage. These three metamorphic complexes belong to the same subduction-metamorphic complex. The pumpellyite–actinolite facies or subfacies can be useful to help reveal the field thermal structure of metamorphic complexes