Laterite profiles developed from granite in southwestern Australia were studied by scanning electron microscopy. The morphology of soil materials reflects the mineralogy of secondary minerals formed from feldspar. In the saprolite, etched feldspar surfaces are coated with kaolinite or radiating, spherical aggregates of tubular halloysite. In the lower pallid zone these minerals have replaced most of the feldspar. In the upper pallid zone a porous framework has developed consisting mainly of quartz and gibbsite with 5-/μm euhedral gibbsite crystals in voids. Halloysite crystals in the upper pallid zone are partly unrolled and have splayed ends. Differences in mineralogy and morphology between profiles are thought to be due to variations in the intensity of leaching.

During an electron microscope study of the weathering of granite from southern New South Wales, Australia, an assemblage of minerals including florencite and rhabdophane was discovered replacing apatite. Light rare earth elements released from allanite early in weathering apparently combined with P released by leaching of primary apatite to form secondary phases exhibiting a range of morphologies and compositions. Chondrite normalized fractionation patterns La > Nd > Sm > Ce; La > Ce > Nd ≥ Sm and La = Sm = Nd > Ce were identified. The rare earth elements were present in very small crystals and aggregates of secondary minerals (< 10 μm) and coexisted with clays and secondary Fe-Ti oxides. The weathered granite was enriched about 6 to 10 times in all rare earth elements except Ce relative to fresh granite if the abundances were corrected for apparent enrichment due to reduction in density. The rare earth elements were probably derived from higher in the weathering profile, possibly by destruction of florencite and rhabdophane in very intensively weathered rock. Ce remained relatively immobile during weathering, probably due to its oxidation to Ce4+.

Lithium-bearing donbassite and tosudite were found in veins in hydrothermally altered granite (Beauvoir granite) in the northern part of the Massif Central, France. The two minerals are characterized by their high Li contents and low Mg and Fe contents; their structural formulae are: $${\left( {S{i_{3.81}}A{l_{0.19}}} \right)_{\Sigma = 4.00}}{O_{10}}{\left( {A{l_{3.81}}L{i_{0.52}}Fe_{0.01}^{2 + }C{a_{0.02}}M{g_{0.01}}} \right)_{\Sigma - 4.38}}{\left( {OH} \right)_8}{\left( {N{a_{0.07}}{K_{0.04}}} \right)_{\Sigma = 0.11}}$$ for donbassite and $${\left( {S{i_{3.50}}A{l_{0.50}}} \right)_{\Sigma = 4.00}}{O_{10}}{\left( {A{l_{2.95}}L{i_{0.22}}Fe_{0.01}^{3 + }T{i_{0.01}}} \right)_{\Sigma = 3.19}}{\left( {OH} \right)_5}{\left( {C{a_{0.01}}N{a_{0.15}}{K_{0.18}}} \right)_{\Sigma = 0.34}}$$ for tosudite.

These chemical compositions indicate that the donbassite is an intermediate member of the donbassite-cookeite solid solution series and that the tosudite consists of interstratified Li-donbassite and beidellite. Both Li-bearing minerals show thermal behavior distinct from those previously reported for dioctahedral chlorite and tosudite.

Petrographie investigation of drill cuttings from the Echassières area indicates that the two minerals were formed in an intermediate stage of hydrothermal alteration following an early stage characterized by formation of muscovite (2M1) at >350°C and before the latest stage characterized by deposition of kaolinite and randomly interstratified illite/smectite at < 100°C. Moreover, tosudite occurs in the upper part of the granite, whereas donbassite is restricted to the lower part, suggesting the formation of tosudite at lower temperatures.

A mineralogical investigation of the highly kaolinized Chanon granite and albite-muscovite granite of the Montebras cupola, Creuse, France, indicates that the magmatic stage was followed by two hydrothermal events related to successive cooling stages and by late weathering. The hydrothermal alteration was accompanied first by greisen formation and then a broad kaolinization process, which pervasively affected the granitic bodies. In the Chanon granite, the greisens are characterized by a trilithionite-lepidolite-quartz-tourmaline assemblage and are surrounded by concentric alteration zones. From the greisen to the fresh granite three zones were distinguished: (1) a zone characterized by secondary brown biotite (<400°C), (2) a zone characterized by secondary green biotite and phengite (300–350°C), and (3) a zone characterized by the presence of corrensite (180°–200°C) located around greisen veinlets. In the albite-muscovite granite the greisen is composed of lepidolite and quartz. This mineral assemblage was followed locally by Li-tosudite crystallization. During the second hydrothermal event (<100°C) an assemblage of kaolinite, mixed-layer illite/smectite (I/S), and illite formed pervasively and in crack fillings; the smectite layers of the US are potassic. Weathering produced Fe oxide and kaolinite. This kind of alteration developed mainly in the overlying Chanon granite. Here, Ca-Mg-montmorillonite formed in subvertical cracks, which transect the two granitic bodies, and hydrothermal I/S was obliterated by Ca-Mg-montmorillonite.

The hydrothermal parageneses were apparently controlled by magmatic albitization and the bulk chemistry of the two granitic bodies. The albitization, the formation of large micaceous greisens, and the successive recrystallizations of biotite (which was the most susceptible phase to alteration) provide information on the temperature range and chemical mobility during successive cooling stages. Si and Mg activities increased as the temperature of alteration decreased, and secondary Mg-biotite and Mg-phengite crystallized as long as the K activity was sufficient. The crystallizations of secondary biotite and phengite were followed by the crystallization of I/S during stages of low K activity. Secondary hydrothermal phases in the Chanon granite contain substantial Fe and Mg. Secondary hydrothermal phases in the albite-muscovite granite contain only small amounts of Fe and Mg, suggesting a lack of chemical exchange between the enclosing Chanon granite and the albite-muscovite granite, which is depleted in Fe-Mg-rich primary phases, such as biotite.

The formation of kaolin-group minerals in the weathering profile of granite, under the humid, temperate climate as found in Korea, was studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and electron microprobe analysis (EMA). The granite was gradually weathered to saprolite. K-rich feldspar was not weathered in the profile, but plagioclase partially weathered to halloysite septa (i.e., wall-like masses). At the bottom of the profile, biotite had weathered to regularly interstratified biotite-vermiculite (B-V), and subsequently to kaolinite, with a considerable increase in grain volume. In the upper part of the profile, loose aggregates of transported clays, including halloysite and kaolinite, coated the preformed halloysite septa in the weathered plagioclase. Halloysite had precipitated as a metastable phase in the microfissures of partially weathered plagioclase. Kaolinite had precipitated heavily in the weathered biotite, where surfaces supply abundant templates facilitating the nucleation of kaolinite. The localized crystallization of halloysite and kaolinite, depending on the distribution of primary minerals, strongly influenced the kaolin mineralogy of the granite weathering profile.

To study the physico-chemical activity of lichens on micaceous components of granitic rocks, samples covered by thalli of Parmelia conspersa (Ehrht) Ach. and Aspicilia intermutans (Nyl.) Arn. were collected and examined with Scanning Electron Microscopy (SEM) equipped with a Back Scattered Electron (BSE) detector and an Energy Dispersive Spectroscopy (EDS) microanalytical system. The bio-physical activity of both lichen species leads to a deep alteration of biotite, which results in detachment, separation and exfoliation of biotite plates. Chemically, the bioweathering process of biotite in the lichenmineral contact zone involves considerable depletion of potassium (K) from interlayer positions in biotite and removal of several elements, corresponding to a 9.7% loss in matter. The sequence of the loss of elements is: K+ » Fetot > Ti4+ ≅ Mg2+. There are also some gains in the order: Ca2+ > Na+ » Al3+ > Si4+ attributed to dissolution of co-existing Ca and Na rich minerals. Geochemical mass balance results suggest the transformation of K-rich biotite to scarcely altered biotite interstratified with a biotite-vermiculite intermediate phase in the lichen bioweathered contact zones.

The question of whether clay minerals can be biogenically transformed as a result of lichen activity at the lichen-rock interface remains unresolved. We applied several microscopical and analytical techniques—scanning electron microscopy-back-scattered electron (SEM-BSE), energy dispersive spectroscopy (EDS) and high-resolution transmission electron microscopy (HRTEM)—in an attempt to address this issue. Unaffected granitic biotite and bioweathered material from the granitic biotite and Parmelia conspersa lichen thalli interface were examined using HRTEM after ultrathin sectioning. The n-alkylammonium treatment of ultrathin sections was carried out in order to study the biogenous mineralogical transformation of the biotite. Microsamples proceeding from unaffected biotite zones demonstrated homogenous 10-Å d(001)-value biotite phase. HRTEM images of lattice fringes of samples taken from the lichen-biotite contact zone reveal large areas of both unexpanded (10-A) and randomly and R = 3 distributed expanded (from 14- to 30-Å) layers of phyllosilicates identified as interstratified biotite-vermiculite. Results of artificial biotite weathering (replacement of K by Ca ion) also revealed the biotite-vermiculite phase formation, indicating that K release in biotite is one of the mechanisms responsible for interstratified mineral phase formation. Two parallel processes, physical exfoliation of biotite and inter-layer ionic exchange of K and subsequent vermiculite formation, are the mechanisms for biotite bioweathering induced by lichens.

The porosity of a propylitized granite from Charroux (France), with no fractures or sealed fractures, increases by more than four times from the unaltered (0.3%) to the altered rock (1.4%). This evolution results from several local porosity modifications which occur at different scales in the rock: (1) at the core scale, from 10−1 to 10−5 m, where rock porosity changes as a function of rock-forming mineralogical composition; (2) at the mineral scale, from 10−3 to 10−7 m, where porosity depends both on the nature of the rock-forming mineral and its clay mineral alteration. Mineralogical and porosity data collected from the granite using a mineralogical map (after chemical staining and scanning electron microscopy images combined with autoradiographs) indicate that (1) the ferromagnesian rock-forming minerals — biotite and magnesiohornblende — act as the main porosity source in the unaltered granite, and (2) the nature of the clay minerals replacing rock-forming minerals in the altered granite appears to control the porosity value through two major alteration processes: chloritization and phengitization which affect the ferromagnesian minerals and produce non-porous chloritic and porous phengitic areas, respectively, at the studied scales. The observation that incipient porosity formation in granites is strongly linked to the pathway of ferromagnesian silicate alteration and subsequent clay mineral formation underlines the need to study parent-rock texture and mineralogy and their effects on subsequent near-surface weathering of granites.

In order to elucidate the process of mineralization of clay minerals in fault gouge and its spatial-temporal relationship with fault-zone evolution and hydrothermal alteration, X-ray diffraction (XRD) analysis and K-Ar dating were performed on clay samples from the Kojaku Granite of central Japan, including fault gouge along an active fault. The area studied is suitable for understanding thermal constraints on clay mineralization because the wall rock is homogeneous and its thermal history well defined. The results from XRD indicated that the clay minerals in the gouge samples are dioctahedral smectite, kaolinite, and 1Md illite, whereas clay fillings in fractures and joints in the intact granite (clay vein) include 2M1 illite in addition to dioctahedral smectite and 1Md illite. The evolution of clay mineralization is reconstructed as follows: (1) high-temperature hydrothermal alteration of feldspar and biotite produced 2M1 illite in clay veins; and (2) alteration accompanied by shearing at a lower temperature resulted in the formation of 1Md illite in the gouges. This scenario is consistent with the cooling history of the granite constrained by fission-track, U-Pb, and K-Ar dating methods. K-Ar dating of the clay samples separated into multiple particle-size fractions indicated that the low-temperature alteration leading to the production of 1Md illite was dated to ~40 Ma. Based on the cooling history of the granite, the 1Md illite formed at temperatures of 60–120°C. This temperature range was at the lower limit of the range reported in previous studies for faults. The spatial and geometrical relation of the faults studied and their K-Ar ages infer evolution which can be described as extensive development of small-scale faults at ~40 Ma followed by coalescence of the small-scale faults to form a larger, recently reactivated, active fault. The K-Ar ages have not been reset by the recent near-surface fault activity.

Eclogite-facies mineral assemblages are commonly preserved in mafic protoliths within continental terranes. It is widely accepted that the entirety of these continental terrains must also have been subducted to eclogite-facies conditions. However, evidence that the felsic material transformed at eclogite-facies conditions is lacking. Low-strain metagranites of the ultrahigh-pressure metamorphic Tso Morari Complex in Ladakh, Himalaya, are host to eclogite-facies mafic sills and preserve evidence of subduction to eclogite-facies conditions. Following the eclogite-facies metamorphism, the granites and their gneissic equivalents were overprinted by amphibolite-facies Barrovian metamorphism, obscuring their earlier metamorphic history. We present evidence that the Tso Morari metagranites preserve a complex magmatic, hydrothermal and polymetamorphic history that involved four stages. Stage 1 was magmatic crystallisation, a record of which is preserved in the primary igneous mineralogy and relict igneous microstructures. Monazite grains record a U–Pb age of 474.0 ± 11.6 Ma, concurrent with a published zircon crystallisation age. Stage 2 represents pervasive late-magmatic hydrothermal alteration of the granite during emplacement and is evident in the mineral composition, particularly in the white micas preserved in the igneous domains. Stage 3 involved the (ultra)high-pressure metamorphism of these granite bodies during the Himalayan subduction of continental material. The high-pressure stage of the metamorphic history (>25 kbar at 550–650°C) is preserved as thin coronas of garnet and phengite around igneous biotite, garnet with kyanite inclusions in pseudomorphs after cordierite, and rare palisade quartz textures after coesite. Stage 4 was a result of Barrovian metamorphism of the Tso Morari Complex and is evident in the replacement of garnet by biotite. Many of these features are preserved in localised textural domains in the rock, where local equilibrium was important and the anhydrous conditions limited reaction progress, though aided preservation potential. Collectively, these four stages record a 480 Myr history of metamorphism and reworking of the northernmost Indian plate.

This study presents zircon U–Pb geochronology and Hf and O isotope data for granitic rocks in the Zijinshan ore field, southwestern Fujian Province, China. The intrusive rocks comprise monzogranite, granite and granodiorite. The magmatic zircon U–Pb ages from these granitic rocks can be divided into four episodes: episodes 1 (157.9–159.9 Ma) and 2 (141 Ma) in the Late Jurassic and episodes 3 (108.1–103.2 Ma) and 4 (97.5–99.7 Ma) in the Middle and Late Cretaceous, respectively. Patterns of rare-earth elements (REE) show enrichment in light REE and obvious negative Eu anomalies. These rocks are also enriched in Rb, Th, U, La, Ce, Nd and Hf, and depleted in Ba, Nb, Sr, P and Ti. The increasing La/Yb ratio and decreasing heavy REE content with decreasing age may imply an increasing contribution of mantle-derived materials from the Late Jurassic to Cretaceous. The zircon ϵ Hf(t) and δ18O values, ranging from −37.7 to −2.8 and 12.0 ‰ to 6.3 ‰, respectively, indicate that the lower crust is an important source of granitic rocks. There was a significant increase in ϵ Hf(t) values and a decrease in δ18O values in the younger magmatic episodes (3 and 4), which ranged from −11.4 to −0.6 and 10.7 to 6.3 ‰, respectively. This suggests an increasing contribution of mantle-derived magma to the crustal melts from the Late Jurassic to late Early Cretaceous in response to the changing regional tectonic setting from compression to extension and an increasing interaction between the crust and mantle.

With the discovery of high-productivity oilfields in granite buried hills, it is necessary to systematically investigate the types of granite weathered reservoirs at different depths and their spatial distribution. However, previously subdivided reservoirs have been assumed to exhibit the same vertical zoning in different structural parts, contradicting the fact that the degree of weathering varies with the topography. In addition, comprehensive and quantitative methods for classifying reservoir types are lacking. Taking the Binxian Uplift of the Dongying depression in Bohai Bay Basin as an example, we therefore established a comprehensive identification standard for dividing granite reservoirs using lithology division, logging curve statistics, a dual-medium matrix–fracture model and seismic facies identification. Subsequently, by combining logging and seismic methods, the vertical stacking types and distribution properties of weathered granite reservoirs in various structural positions were analysed. The reservoirs were divided vertically into three zones: regolith, dissolution and fracture. Quantitative logging response standards for the different reservoirs were established using acoustic, density, natural gamma and resistivity logging. In terms of the seismic response, the regolith, dissolution and fracture zone corresponded to high-, medium- and low-amplitude seismic facies, respectively. A dynamic double-layer structure of the reservoir was established, comprising a completely weathered layer and a semi-weathered layer. The reservoir division method proposed in this paper can be used in other areas, and the research results can help promote the exploration of granite buried hill reservoirs.

Often understudied by archaeologists, ground stone tools (GST) were ubiquitous in the ancient Maya world. Their applications ranged from household tools to ceremonial equipment and beyond. Little attention has been focused on chemically sourcing the raw stone material used in GST production, largely because these tools were fashioned out of igneous or sedimentary rock, which can present characterization challenges. And, although portable X-ray fluorescence (pXRF) has been applied widely to source obsidian, the utility of pXRF for geochemically sourcing other kinds of stone remains underexplored. We present a small-scale application of pXRF for determining granite provenance within a section of the Middle Belize Valley in Belize, Central America. Belize is an ideal location to test chemical sourcing studies of granite because there are only three tightly restricted and chemically distinct sources of granite in the country, from which the overwhelming majority of granite for ancient tool production derived. The method described here demonstrates that successful and accurate geological characterizations can be made on granite GST. This cutting-edge sourcing technique has the potential to be more widely applied in other regions to reveal deeper connections between the sources of GST production and sites of consumption across space and through time.

The Himalaya is characterized by the presence of both pre-Himalayan Palaeozoic and syn-Himalayan Cenozoic granitic bodies, which can help unravel the pre- to syn-collisional geodynamics of this orogen. In the Bhagirathi Valley of Western Himalaya, such granites and the Tethyan Himalayan Sequence (THS) hosting them are bound to the south by the top-to-the-N extensional Jhala Normal Fault (JNF) and low-grade metapelite of the THS to its north. The THS is intruded by a set of leucocratic dykes concordant to the JNF. Zircon U–Pb laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) geochronology of the THS and one leucocratic dyke reveals that the two rocks have a strikingly similar age distribution, with a common and most prominent age peak at ~1000 Ma. To the north of the THS lies Bhaironghati Granite, a Palaeozoic two-mica granite, which shows a crystallization age of 512.28 ± 1.58 Ma. Our geochemical analysis indicates that it is a product of pre-Himalayan Palaeozoic magmatism owing to extensional tectonics in a back-arc or rift setting following the assembly of Gondwana (500–530 Ma). The Cenozoic Gangotri Leucogranite lies to the north of Bhaironghati Granite, and U–Pb dating of zircon from this leucogranite gives a crystallization age of 21.73 ± 0.11 Ma. Our geochemical studies suggest that the Gangotri Leucogranite is a product of muscovite-dehydration melting of the lower crust owing to flexural bending in relation to steepening of the subducted Indian plate. The leucocratic dykes are highly refracted parts of the Gangotri Leucogranite that migrated and emplaced along extensional fault zones related to the JNF and scavenged zircon from the host THS during crystallization.

The Souter Head sub-volcanic complex (Aberdeenshire, Scotland) intruded the high-grade metamorphic core of the Grampian Orogen at 469.1 ± 0.6 Ma (uranium-238–lead-206 (238U–206Pb) zircon). It follows closely peak metamorphism and deformation in the Grampian Terrane and tightly constrains the end of the Grampian Event of the Caledonian Orogeny. Temporally coincident U–Pb and argon/argon (40Ar/39Ar) data show the complex cooled quickly with temperatures decreasing from ca.800 °C to less than 200 °C within 1 Ma. Younger rhenium–osmium (Re–Os) ages are due to post-emplacement alteration of molybdenite to powellite. The U–Pb and Ar/Ar data combined with existing geochronological data show that D2/D3 deformation, peak metamorphism (Barrovian and Buchan style) and basic magmatism in NE Scotland were synchronous at ca.470 Ma and are associated with rapid uplift (5–10 km Ma−1) of the orogen, which, by ca.469 Ma, had removed the cover to the metamorphic pile. Rapid uplift resulted in decompressional melting and the generation of mafic and felsic magmatism. Shallow slab break-off (50–100 km) is invoked to explain the synchroneity of these events. This interpretation implies that peak metamorphism and D2/D3 ductile deformation were associated with extension. Similarities in the nature and timing of orogenic events in Connemara, western Ireland, with NE Scotland suggest that shallow slab break-off occurred in both localities.

A form of natural rock marking is described from a site on the coast of Fujian in China. Having been defined as rock art, it has now been found to be natural, caused by the release of massive kinetic energy in collisions between large blocks of granite. A combination of compressive and tensile stresses has yielded geometric changes to the fabric of the rock, and the selective weathering of modified parts of the rock has produced visually distinct, large surface markings resembling a rising Sun. The processes involved are considered in the light of research into the similar effects of explosives on rock.

A geochemical and mineralogical study has allowed us to address the factors controlling distribution pattern, residence and behaviour of rare earth elements (REE) during kaolinization of Variscan granitoids in NW Spain. Mineral composition of the deeply weathered samples is dominated by kaolinite, with minor amounts of quartz, muscovite-illite, alkaline feldspar and traces of resistant minerals (rutile, ilmenite, zircon and monazite). Variable amounts of Si, Na, Ca, K, Rb, Cs, Ba, U and P were lost from the weathering profile, as a result of feldspars, mica and apatite breakdown, whereas Al, Fe, Ti, Zr, Th, Hf and REE were concentrated in the residual kaolin. Chondrite-normalized REE patterns of the kaolins show an overall enrichment of light REE (LaN/SmN = 1.22–2.53), heavy REE depletion (GdN/YbN = 2.42–15.10) and a strong negative Eu anomaly (Eu/Eu* = 0.11–0.25), probably inherited from the parent granite. Nevertheless, the normalization to the parent granite reveals some REE fractionation and increasing positive Eu anomalies with advancing weathering, in response to the breakdown of feldspars. Different grain-size fractions show similar REE distribution patterns, but differ in concentration levels. Although the fine fractions are the most important REE reservoir, there is no positive correlation with clay mineralogy. The correlative behaviour among P2O5, Th and REE in the <2 mm fraction suggests that monazite plays a dominant role controlling the REE budget in the weathering profile.

Smectite formation in a vertisol developed from a granitic parent rock in the Kaélé region of Cameroon in a tropical, dry climate was studied by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), chemical analyses, cation exchange capacity (CEC) and low temperature gas adsorption. The soil profile comprises three horizons (from base to top): (1) a saprolite, (2) an intermediate horizon, and (3) an upper dark grey horizon. In the saprolite, the progressive alteration of feldspars gave rise to the exclusive neoformation of beidellite exhibiting a typical honeycomb fabric. This process resulted in Al, Fe, Ca, Mg, Ti and Mn enrichment, a depletion of Si and Na and a significant negative Eu anomaly. In the upper horizons, beidellite evolves and is transformed into montmorillonite and kaolinite, probably through a series of smectite-kaolinite mixed layers. This transformation, from the saprolite to the upper horizons, causes the observed decrease in the CEC and the increase in specific surface area and mesoporosity of the clay. The REE patterns of the bulk soil and clay fraction display similar behaviour, indicating that the three horizons, and hence the clay minerals, have a common source in the underlying granite. Mass-balance calculations show that the intense weathering of the granite leads to a mass reduction of ~80–90%.

Alkali feldspar phenocrysts (bulk composition Or75.0Ab24.6An0.4) in the subsolvus Shap granite comprise a fine-scale mixture of subregular pristine crypto- and micro-perthites with altered, micropore-rich feldspar with irregular microstructures. The regular perthites are strain-controlled intergrowths of Albite and/or Periclinetwinned albite exsolution lamellae within tweed orthoclase. The microperthites formed at ⩽ 590°C by heterogeneous nucleation of thin albite films which coarsened to > 1 µm length. Cryptoperthites developed at < 400°C by homogeneous nucleation of sub-µm long platelets between films. Platelets are coherent, but the coarser microperthite lamellae are semi-coherent, with pairs of misfit dislocations sub-regularly spaced along the albite-orthoclase interface. As much as 30% of any one feldspar crystal is turbid, a result of the formation of numerous µm to sub-µm sized micropores during deuteric alteration. In some areas, deuteric fluids gained access to the interior of feldspar crystals by exploiting semi-coherent film lamellae. Albite was selectively dissolved and micropore-rich irregular microcline was reprecipitated in its place. In other parts of the feldspars deuteric recrystallization completely cross-cuts the pristine microtextures and patch perthites have formed. These are coarse, incoherent to semi-coherent intergrowths of irregular microcline (replacing tweed orthoclase) and Albite-twinned albite. The deuteric reactions occurred at < 400°C; the main driving force for dissolution and reprecipitation was decrease in the elastic strain energy at the coherent interfaces of crypto-and micro-perthite lamellae, and the recrystallization of tweed orthoclase to irregular microcline.

Garnet is a widespread minor accessory mineral in the Late Proterozoic Elat-Quarry granite of southern Israel and is more abundant in the associated pegmatite and aplite. All garnets are dominated by almandine and spessartine end-members. Granite-hosted garnets are zoned with relative enrichment of Mn in the core and Fe in the rim. The chemistry of the garnet in the pegmatite and aplite are comparable to the rim compositions of garnets in the granite, but with a slight Fe-depletion at the rims. Geochemical parameters for the granite indicate fractional crystallization largely of an S-type source magma to a peraluminous composition.

In the highly evolved granite magma, Fe is relatively diminished, and only small amounts of biotite can crystallize. Manganese becomes a compatible element forming Mn-rich garnet (cores), and reducing the Mn content in the magma, subsequently leading to Fe-enriched rims. The greater abundance of garnet in the pegmatite and aplite (and its larger crystal-size in the former) relate to the enhanced presence of a hydrous fluid within the magma. The tendency for garnet crystals to concentrate in bands is much more developed in the pegmatite than in the granite, and is associated with the effects of hydrofracturing (fracture-filling), and the crystallization of coarse-grained alkaline feldspars.