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Storage timescales and the crystal growth history recorded in the layered reservoir of the Unit 3 Kulanaokuaiki Tephra Member of the Uēkahuna Ash from Kīlauea volcano

The Kulanaokuaiki Tephra Unit 3 (900 C.E.) was a subplinian basaltic scoria eruption, the largest known to have occurred at Kīlauea’s summit. The initiation mechanism and cause(s) of this highly hazardous eruption remain poorly understood, particularly as this style of activity has not been observed in the modern period. We use olivine diffusion timescales from Fe-Mg and lithium zoning to assess magma storage timescales and evaluate evidence for mixing prior to eruption. Of the 200 crystals assessed, 55% are normally zoned for forsterite and 45% are non-zoned. Zoned crystals (> 1 mm) ( n = 96) have average compositions of Fo 89 cores and Fo 81 rims, while small crystals 0.5–1 mm ( n = 14) have Fo 85 cores and Fo 82 rims. Modeled Fo diffusion timescales range from < 1 to 12.6 years (median of 3.0 years). Lithium maps in 32 of the forsterite-zoned crystals reveal a variety of lithium zoning types, most of which we attribute to crystal growth. Many lithium profiles are coupled to phosphorus within the outer ~ 100 μm of the crystal ( n = 17), reflecting growth processes and precluding their use for diffusion studies. Overall, our Unit 3 olivine dataset displays no evidence of magmatic priming shortly prior to eruption, unlike prior observations for the basaltic subplinian eruption of the Keanakāko‘i Tephra Unit E (1650 C.E.). Thus, explosive eruption magmas may be stored for considerably longer than previously thought, and magmatic priming is not a necessary precursor for Kīlauea’s explosive eruptions. We hypothesize that gas-driven filter pressing from crystallization of microlites and macrocrysts in the reservoir slurry contributed to the explosivity of the Unit 3 eruption.

Hawaii

Magma storage and mixing conditions for the 1953-1974 eruption of Southwest Trident volcano, Katmai National Park, Alaska

Between 1953 and 1974, approximately 0.5 km 3 of andesite and dacite erupted from a new vent on the southwest flank of Trident volcano in Katmai National Park, Alaska, forming an edifice now known as Southwest (or New) Trident. Field, analytical, and experimental evidence shows that the eruption commenced soon after mixing of dacite and andesite magmas at shallow crustal levels. Four lava flows (58.3–65.5 wt% SiO 2 ) are the dominant products of the eruption; these contain discrete andesitic enclaves (55.8–58.9 wt% SiO 2 ) as well as micro- and macro-scale compositional banding. Tephra from the eruption spans the same compositional range as lava flows; however, andesite scoria (56–58.1 wt% SiO 2 ) is more abundant relative to dacite tephra, and is the explosively erupted counterpart to andesite enclaves. Fe–Ti oxide pairs from andesite scoria show a limited temperature range, clustered around 1000 °C. Temperatures from grains found in dacite lavas possess a wider range; however, cores from large (>100 μm) magnetite and coexisting ilmenite give temperatures of ∼890 °C, taken to represent a pre-mixing temperature for the dacite. Water contents from dacite phenocryst melt inclusions and phase equilibria experiments on the andesite imply that the two magmas last resided at a water pressure of 90 MPa, and contained ∼3.5 wt% H 2 O, equivalent to 3 km depth if saturated. Unzoned pyroxene and sodic plagioclase in the dacite suggest that it likely underwent significant crystallization at this depth; highly resorbed anorthitic plagioclase from the andesite suggests that it originated at greater depths and underwent relatively rapid ascent until it reached 3 km, mixed with dacite, and erupted. Diffusion profiles in phenocrysts suggest that mixing preceded eruption of earliest lava by approximately one month. The lack of a compositional gap in the erupted rock suite indicates that thorough mixing of the andesite and dacite occurred quickly, via disaggregation of enclaves, phenocryst transfer from one magma to another, and direct mixing of compositionally distinct melt phases.

Alaska

Adiabatic temperature changes of magma-gas mixtures during ascent and eruption

Most quantitative studies of flow dynamics in eruptive conduits during volcanic eruptions use a simplified energy equation that ignores either temperature changes, or the thermal effects of gas exsolution. In this paper we assess the effects of those simplifications by analyzing the influence of equilibrium gas exsolution and expansion on final temperatures, velocities, and liquid viscosities of magma–gas mixtures during adiabatic decompression. For a given initial pressure ( p 1 ), temperature ( T 1 ) and melt composition, the final temperature ( T f ) and velocity ( u max ) will vary depending on the degree to which friction and other irreversible processes reduce mechanical energy within the conduit. The final conditions range between two thermodynamic end members: (1) constant enthalpy ( dh =0), in which T f is maximal and no energy goes into lifting or acceleration; and (2) constant entropy ( ds =0), in which T f is minimal and maximum energy goes into lifting and acceleration. For ds =0, T 1 =900 °C and p 1 =200 MPa, a water-saturated albitic melt cools by ~200 °C during decompression, but only about 250 °C of this temperature decrease can be attributed to the energy of gas exsolution per se: the remainder results from expansion of gas that has already exsolved. For the same T 1 and p 1 , and dh =0, T f is 10–15 °C hotter than T 1 but is about 10–25 °C cooler than T f in similar calculations that ignore the energy of gas exsolution. For ds =0, p 1 =200 MPa and T 1 =9,000 °C, assuming that all the enthalpy change of decompression goes into kinetic energy, a water-saturated albitic mixture can theoretically accelerate to ~800 m/s. Similar calculations that ignore gas exsolution (but take into account gas expansion) give velocities about 10–15% higher. For the same T 1 , p I =200 MPa, and ds =0, the cooling associated with gas expansion and exsolution increases final melt viscosity more than 2.5 orders of magnitude. For dh =0, isenthalpic heating decreases final melt viscosity by about 0.7 orders of magnitude. Thermal effects of gas exsolution are responsible for less than 10% of these viscosity changes. Isenthalpic heating could significantly reduce flow resistance in eruptive conduits if heat generation were concentrated along conduit walls, where shearing is greatest. Isentropic cooling could enhance clast fragmentation in near-surface vents in cases where extremely rapid pressure drops reduce gas temperatures and chill the margins of expanding pyroclasts.

Contributions to Mineralogy and Petrology

Evidence of hydrous differentiation and crystal accumulation in the low-MgO, high-Al2O3 Lake Basalt from Medicine Lake volcano, California

The late Pleistocene Lake Basalt of Medicine Lake volcano, California is comprised of variably porphyritic basalt and basaltic andesite flows and scoria. These eruptives are similar in composition and phenocryst abundance to the low-MgO, high-Al 2 O 3 mafic magmas common in convergent margin settings. The petrogenesis of the magmas that produced the Lake Basalt has been inferred from field relations, melting experiments and subsequent major and trace element modeling. Their formation involved both hydrous differentiation and plagioclase accumulation and thus the Lake Basalt can be used to constrain the relative contributions of these processes to the production of high-Al 2 O 3 arc basalt. Phenocryst-poor lavas of the Lake Basalt formed by hydrous differentiation; their compositions and observed phenocrysts were reproduced in 1 kbar, H 2 O-saturated melting experiments. Anorthite-rich plagioclase compositions of the lavas of the Lake Basalt necessitate crystallization from melts with between 4 and 6 wt% dissolved H 2 O. Phenocryst-rich lavas of the Lake Basalt, with 18 modal% phenocrysts and greater, formed by plagioclase accumulation in magmas similar to the phenocryst-poor lavas. This interpretation is supported by the depleted incompatible element abundances and enriched Sr/Zr ratio of the more porphyritic lavas relative to the phenocryst-poor lavas. We model the formation of the Lake Basalt as a two-stage process that combines a differentiation model and a plagioclase accumulation model. Stage one involved hydrous fractionation, granitic assimilation and mixing with undifferentiated parent magma. This process generated lavas with up to 19.2 wt% A1 2 O 3 and 7 modal% phenocrysts. In stage two, plagioclase accumulated in these liquids and produced more aluminous and porphyritic lavas with up to 21.8 wt% A1 2 O 3 and 33 modal% phenocrysts.

California

Influence of stretching and density contrasts on the chemical evolution of continental magmas: An example from the Ivrea-Verbano Zone

The southern Ivrea-Verbano Zone of the Italian Western Alps contains a huge mafic complex that intruded high-grade metamorphic rocks while they were resident in the lower crust. Geologic mapping and chemical variations of the igneous body were used to study the evolution of underplated crust. Slivers of crustal rocks (septa) interlayered with igneous mafic rocks are concentrated in a narrow zone deep in the complex (Paragneiss-bearing Belt) and show evidence of advanced degrees of partial melting. Variations of rare-earth-element patterns and Sr isotope composition of the igneous rocks across the sequence are consistent with increasing crustal contamination approaching the septa. Therefore, the Paragneiss-bearing Belt is considered representative of an “assimilation region” where in-situ interaction between mantle- and crust-derived magmas resulted in production of hybrid melts. Buoyancy caused upwards migration of the hybrid melts that incorporated the last septa and were stored at higher levels, feeding the Upper Mafic Complex. Synmagmatic stretching of the assimilation region facilitated mixing and homogenization of melts. Chemical variations of granitoids extracted from the septa show that deep septa are more depleted than shallow ones. This suggests that the first incorporated septa were denser than the later ones, as required by the high density of the first-injected mafic magmas. It is inferred that density contrasts between mafic melts and crustal rocks play a crucial role for the processes of contamination of continental magmas. In thick under plated crust, the extraction of early felsic/hybrid melts from the lower crust may be required to increase the density of the lower crust and to allow the later mafic magmas to penetrate higher crustal levels.

Contributions to Mineralogy and Petrology

Magmatic infiltration and melting in the lower crust and upper mantle beneath the Cima volcanic field, California

Xenoliths of lower crustal and upper mantle rocks from the Cima volcanic field (CVF) commonly contain glass pockets, veins, and planar trains of glass and/or fluid inclusions in primary minerals. Glass pockets occupy spaces formerly occupied by primary minerals of the host rocks, but there is a general lack of correspondence between the composition of the glass and that of the replaced primary minerals. The melting is considered to have been induced by infiltration of basaltic magma and differentiates of basaltic magma from complex conduits formed by hydraulic fracturing of the mantle and crustal rocks, and to have occurred during the episode of CVF magmatism between ∼7.5 Ma and present. Variable compositions of quenched melts resulted from mixing of introduced melts and products of melting of primary minerals, reaction with primary minerals, partial crystallization, and fractionation resulting from melt and volatile expulsion upon entrainment of the xenoliths. High silica melts ( >∼60% SiO 2 ) may result by mixing introduced melts with siliceous melts produced by reaction of orthopyroxene. Other quenched melt compositions range from those comparable to the host basalts to those with intermediate Si compositions and elevated Al, alkalis, Ti, P, and S; groundmass compositions of CVF basalts are consistent with infiltration of fractionates of those basalts, but near-solidus melting may also contribute to formation of glass with intermediate silica contents with infiltration only of volatile constituents.

California

Plagioclase zonation styles in hornblende gabbro inclusions from Little Glass Mountain, Medicine Lake volcano, California: Implications for fractionation mechanisms and the formation of composition gaps

The rhyolite of Little Glass Mountain (73–74% SiO 2 ) is a single eruptive unit that contains inclusions of quenched andesite liquid (54–61% SiO 2 ) and partially crystalline cumulate hornblende gabbro (53–55% SiO 2 ). Based on previous studies, the quenched andesite inclusions and host rhyolite lava are related to one another through fractional crystallization and represent an example of a fractionation-generated composition gap. The hornblende gabbros represent the cumulate residue associated with the rhyolite-producing and composition gap-forming fractionation event. This study combines textural (Nomarski Differential Interference Contrast, NDIC, imaging), major element (An content) and trace element (Mg, Fe, Sr, K, Ti, Ba) data on the style of zonation of plagioclase crystals from representative andesite and gabbro inclusions, to assess the physical environment in which the fractionation event and composition gap formation took place. The andesite inclusions (54–61% SiO 2 ) are sparsely phyric with phenocrysts of plagioclase, augite and Fe-oxide±olivine, +/–orthopyroxene, +/–hornblende set within a glassy to crystalline matrix. The gabbro cumulates (53–55% SiO 2 ) consist of an interconnected framework of plagioclase, augite, olivine, orthopyroxene, hornblende and Fe-oxide along with highly vesicular interstitial glass (70–74% SiO 2 ). The gabbros record a two-stage crystallization history of plagioclase+olivine+augite (Stage I) followed by plagioclase+orthopyroxene+ hornblende+Fe-oxide (Stage II). Texturally, the plagioclase crystals in the andesite inclusions are characterized by complex, fine-scale oscillatory zonation and abundant dissolution surfaces. Compositionally (An content) the crystals are essentially unzoned from core-to-rim. These features indicate growth within a dynamic (convecting?), reservoir of andesite magma. In contrast, the plagioclase crystals in the gabbros are texturally smooth and featureless with strong normal zonation from An 74 at the core to around An 30 . K, and Ba abundances increase and Mg abundances decrease steadily towards the rim. Ti, Fe, and Sr abundances increase and then decrease towards the rim. The trace element variations are fully consistent with the two-stage crystallization sequence inferred from the gabbro mineralogy. These results indicate progressive closed-system in situ crystallization in a quiescent magmatic boundary layer environment located along the margins of the andesite magma body. The fractional crystallization that generated the host rhyolite lava is one of inward solidification of a crystallizing boundary layer followed by melt extraction and accumulation of highly evolved interstitial liquid. This mechanism explains the formation of the composition gap between parental andesite and rhyolite magma compositions.

California

Late-stage sulfides and sulfarsenides in Lower Cambrian black shale (stone coal) from the Huangjiawan mine, Guizhou Province, People's Republic of China

The Ni-Mo Huangjiawan mine, Guizhou Province, People's Republic of China, occurs in Lower Cambrian black shale (stone coal) in an area where other mines have recently extracted ore from the same horizon. Detailed electron microprobe (EMPA) and scanning electron microscope (SEM) analyses of representative thin sections have revealed a complex assemblage of sulfides and sulfarsenides. Early sulfidic and phosphatic nodules and host matrix have been lithified, somewhat fractured, and then mineralized with later-stage sulfides and sulfarsenides. Gersdorffite, millerite, polydymite, pyrite, sphalerite, chalcopyrite, galena, and clausthalite have been recognized. EMPA data are given for the major phases. Pyrite trace-element distributions and coeval Ni-, As-sulfides indicate that in the main ore layer, the last sulfide deposition was Ni-As-Co-rich. Mo and V deposition were early in the petrogenesis of these rocks. The assemblages gersdorffite-millerite-polydymite (pyrite) and millerite-gersdorffite (pyrite) and the composition of gersdorffite indicate a formation temperature of between 200?? and 300??C suggesting that the last solutions to infiltrate and mineralize the samples were related to hydrothermal processes. Environmentally sensitive elements such as As, Cd, and Se are hosted by sulfides and sulfarsenides and are the main source of these elements to residual soil. Crops grown on them are enriched in these elements, and they may be hazardous for animal and human consumption. ?? Springer-Verlag 2007.

Mineralogy and Petrology

Zircon from historic eruptions in Iceland: Reconstructing storage and evolution of silicic magmas

Zoning patterns, U-Th disequilibria ages, and elemental compositions of zircon from eruptions of Askja (1875 AD), Hekla (1158 AD), Öræfajökull (1362 AD) and Torfajökull (1477 AD, 871 AD, 3100 BP, 7500 BP) provide insights into the complex, extended, histories of silicic magmatic systems in Iceland. Zircon compositions, which are correlated with proximity to the main axial rift, are distinct from those of mid-ocean ridge environments and fall at the low-Hf edge of the range of continental zircon. Morphology, zoning patterns, compositions, and U-Th ages all indicate growth and storage in subvolcanic silicic mushes or recently solidified rock at temperatures above the solidus but lower than that of the erupting magma. The eruptive products were likely ascending magmas that entrained a zircon “cargo” that formed thousands to tens of thousands of years prior to the eruptions.

Mineralogy and Petrology

Sphene and zircon in the Highland Range volcanic sequence (Miocene, southern Nevada, USA): Elemental partitioning, phase relations, and influence on evolution of silicic magma

Sphene is prominent in Miocene plutonic rocks ranging from diorite to granite in southern Nevada, USA, but it is restricted to rhyolites in coeval volcanic sequences. In the Highland Range volcanic sequence, sphene appears as a phenocryst only in the most evolved rocks (72–77 mass% SiO 2 ; matrix glass 77–78 mass% SiO 2 ). Zr-in-sphene temperatures of crystallization are mostly restricted to 715 and 755°C, in contrast to zircon (710–920°C, Ti-in-zircon thermometry). Sphene rim/glass Kds for rare earth elements are extremely high (La 120, Sm 1200, Gd 1300, Lu 240). Rare earth elements, especially the middle REE (MREE), decrease from centers to rims of sphene phenocrysts along with Zr, demonstrating the effect of progressive sphene fractionation. Whole rocks and glasses have MREE-depleted, U-shaped REE patterns as a consequence of sphene fractionation. Within the co-genetic, sphene-rich Searchlight pluton, only evolved leucogranites show comparable MREE depletion. These results indicate that sphene saturation in intruded and extruded magmas occurred only in highly evolved melts: abundant sphene in less silicic plutonic rocks represents a late-stage ‘bloom’ in fractionated interstitial melt.

Nevada

Mineralogical, chemical, and crystallographic properties of supergene jarosite-group minerals from the Xitieshan Pb-Zn sulfide deposit, northern Tibetan Plateau, China

Supergene jarosite-group minerals are widespread in weathering profiles overlying Pb-Zn sulfide ores at Xitieshan, northern Tibetan Plateau, China. They consist predominantly of K-deficient natrojarosite, with lesser amounts of K-rich natrojarosite and plumbojarosite. Electron microprobe (EMP) analyses, scanning electron microcopy (SEM) investigation, and X-ray mapping reveal that the jarosite-group minerals are characterized by spectacular oscillatory zoning composed of alternating growth bands of K-deficient and K-bearing natrojarosite (K 2 O >1 wt.%). Plumbojarosite, whenever present, occurs as an overgrowth in the outermost bands, and its composition can be best represented by K 0.29 Na 0.19 Pb 0.31 Fe 2.66 Al 0.22 (SO 4 ) 1.65 (PO 4 ) 0.31 (AsO 4 ) 0.04 (OH) 7.37 . The substitution of monovalent for divalent cations at the A site of plumbojarosite is charge balanced by the substitution of five-valent for six-valent anions in XO, 4/sub> at the X site. Thermogravimetric analysis (TGA) of representative samples reveal mass losses of 11.46 wt.% at 446.6 &deg;C and 21.42 wt.% at 683.4 &deg;C due to dehydroxylation and desulfidation, respectively. TGA data also indicate that the natrojarosite structure collapses at 446.6 &deg;C, resulting in the formation of NaFe(SO 4 ) 2 and minor hematite. The decomposition products of NaFe(SO 4 ) are hematite and Na, 2 SO 4 . Powder X-ray diffraction (XRD) analyses show that the jarosite-group minerals have mean unit-cell parameters of a =7.315 &auml; and c =016.598 &auml;. XRD and EMP data support the view that substitutions of Na for K in the A site and full Fe occupancy in the B site can considerably decrease the unit-cell parameter c , but only slightly increase a . The results from this study suggest that the observed oscillatory zoning of jarosite-group minerals at Xitieshan resulted mainly from substitutions of K for Na at the A site and P for S at the X site.

Tibetan Plateau

New constraints on the pyroclastic eruptive history of the Campanian volcanic Plain (Italy)

The &sim;&thinsp;150&thinsp;km 3 (DRE) trachytic Campanian Ignimbrite, which is situated north-west of Naples, Italy, is one of the largest eruptions in the Mediterranean region in the last 200&thinsp;ky. Despite centuries of investigation, the age and eruptive history of the Campanian Ignimbrite is still debated, as is the chronology of other significant volcanic events of the Campanian Plain within the last 200&ndash;300&thinsp;ky. New 40 Ar/ 39 Ar geochronology defines the age of the Campanian Ignimbrite at 39.28&thinsp;&plusmn;&thinsp;0.11&thinsp;ka, about 2&thinsp;ky older than the previous best estimate. Based on the distribution of the Campanian Ignimbrite and associated uppermost proximal lithic and polyclastic breccias, we suggest that the Campanian Ignimbrite magma was emitted from fissures activated along neotectonic Apennine faults rather than from ring fractures defining a Campi Flegrei caldera. Significantly, new volcanological, geochronological, and geochemical data distinguish previously unrecognized ignimbrite deposits in the Campanian Plain, accurately dated between 157 and 205&thinsp;ka. These ages, coupled with a xenocrystic sanidine component >&thinsp;315&thinsp;ka, extend the volcanic history of this region by over 200&thinsp;ky. Recent work also identifies a pyroclastic deposit, dated at 18.0&thinsp;ka, outside of the topographic Campi Flegrei basin, expanding the spatial distribution of post-Campanian Ignimbrite deposits. These new discoveries emphasize the importance of continued investigation of the ages, distribution, volumes, and eruption dynamics of volcanic events associated with the Campanian Plain. Such information is critical for accurate assessment of the volcanic hazards associated with potentially large-volume explosive eruptions in close proximity to the densely populated Neapolitan region.

Mineralogy and Petrology

Isotope geochemistry and fluid inclusion study of skarns from Vesuvius

We present new mineral chemistry, fluid inclusion, stable carbon and oxygen, as well as Pb, Sr, and Nd isotope data of Ca-Mg-silicate-rich ejecta (skarns) and associated cognate and xenolithic nodules from the Mt. Somma-Vesuvius volcanic complex, Italy. The typically zoned skarn ejecta consist mainly of diopsidic and hedenbergitic, sometimes "fassaitic" clinopyroxene, Mg-rich and Ti-poor phlogopite, F-bearing vesuvianite, wollastonite, gehlenite, meionite, forsterite, clinohumite, anorthite and Mg-poor calcite with accessory apatite, spinell, magnetite, perovskite, baddeleyite, and various REE-, U-, Th-, Zr- and Ti-rich minerals. Four major types of fluid inclusions were observed in wollastonite, vesuvianite, gehlenite, clinopyroxene and calcite: a) primary silicate melt inclusions (THOM = 1000-1050??C), b) CO2 ?? H2S-rich fluid inclusions (THOM = 20-31.3??C into the vapor phase), c) multiphase aqueous brine inclusions (THOM = 720-820??C) with mainly sylvite and halite daughter minerals, and d) complex chloride-carbonate-sulfate-fluoride-silicate-bearing saline-melt inclusions (THOM = 870-890??C). The last inclusion type shows evidence for immiscibility between several fluids (silicate melt - aqueous chloride-rich liquid - carbonate/sulfate melt?) during heating and cooling below 870??C. There is no evidence for fluid circulation below 700??C and participation of externally derived meteoric fluids in skarn formation. Skarns have considerably variable 206Pb/204Pb (19.047-19.202), 207Pb/204Pb (15.655-15.670), and 208Pb/204Pb (38.915-39.069) and relatively low 143Nd/144Nd (0.51211-0.51244) ratios. The carbon and oxygen isotope compositions of skarn calcites (??13CV-PDB = -5.4 to -1.1???; ??18OV-SMOW = 11.7 to 16.4???) indicate formation from a 18O- and 13C-enriched fluid. The isotope composition of skarns and the presence of silicate melt inclusion-bearing wollastonite nodules suggests assimilation of carbonate wall rocks by the alkaline magma at moderate depths (< 5 km) and consequent exsolution of CO2-rich vapor and complex saline melts from the contaminated magma that reacted with the carbonate rocks to form skarns.

Mineralogy and Petrology

A metallogenic survey of alkalic rocks of Mt. Somma-Vesuvius volcano

Somma-Vesuvius is an alkaline volcano whose products (pumice, scoria and lava) have alkaline (Na2O+K2O) contents between 6 and 16 wt%, Mg number <50, SiO2 59-47 wt% and MgO 0-7.8 wt% (more than 50% of the samples have a content <2 wt%). Immobile-element ratios (Th/Yb, Ta/Yb, Ce/Yb) indicate a shoshonitic character, while the K2O content (4-10 wt%) is characteristic of ultrapotassic rocks. The behavior of selected metals is discussed by grouping them on the basis of the stratigraphic sequence and differentiating the volcanic activity between plinian and interplinian (Rolandi et al., 1998; Ayuso et al., 1998). This allows observation of the variation within each formation from 25.000y. BP to the last historic eruptive cycle (1631-1944 AD). The main processes to explain the wide distribution of the data presented are fractional crystallization of a mantle-derived magma, magma mixing, and contamination with heterogeneous lower and/or upper crust. Variation diagrams distinguish different behavior for groups of metals: Ag (0.01-0.2 ppm), Mo (1-8.8 ppm), W (1.3-13 ppm), Pb (16-250 ppm), Sb (0.2-2.6 ppm), Sc (0.2-61 ppm), Li (15-140 ppm) and Be (1-31 ppm) increase with increasing differentiation and tend to correlate with the incompatible trace elements (Th, Hf, etc). Cu (10-380 ppm), Au (2-143 ppb), Co (0.7-35.1 ppm) and Fe (1.3-6.2 wt%) decrease towards advanced stage of differentiation. Iron also identifies three magmatic groups. The ratio Fe3+/Fe2+ ranges between 0.2 and 1.8, and Fe2O3/ (Fe2O3+FeO) ranges between 0.2 and 0.8, giving rise to an oxidized environment; exceptions are in the samples belonging to the interplinian formations: I, II, medieval and 1631-1994 AD. Fluorine ranges between 0.1 and 0.4 wt% for the complete Mt. Somma-Vesuvius activity, except for the Ottaviano and Avellino plinian (0.8 wt%) events. Chlorine has a wider range, from 0.1 wt% to 1.6 wt%. Mt Somma-Vesuvius has some features similar to those of mineralized alkaline magmatic systems which coincide with the transition between subduction-related compression and extension-related to continental rifting. We infer that a prospective time for the formation of mineralization at Mt Somma-Vesuvius was during the 1631-1944 eruptive period.

Mineralogy and Petrology

Lunar ferroan anorthosites: mineralogy, compositional variations, and petrogenesis

Detailed petrologic study of a suite of lunar ferroan anorthosites indicates that their mineral compositional variations are generally consistent with derivation of these anorthosites from a common parent magma. There are continuous compositional variations in major elements and smooth trends in minor elements (Mg, Fe in plagioclase; Al, Ti, Cr in pyroxene). Relict textures, zoning, and possible primary trends of mineral compositional variations are preserved in many of the anorthosites. The presence of heterogeneous, bimodal, and/or trimodal pyroxene compositions suggests that some of the anorthosites are polymict rocks; however, they are composed entirely of ferroan-anorthosite-suite lithologies. Some aspects of the mineral composition data suggest that complex processes operated during formation of the ferroan anorthosites. The lack of a well-defined, positive or negative trend of pyroxene Mg/(Mg + Fe) versus plagioclase anorthite content, the homogenization of mineral compositions in some anorthosites, and the varied and apparently enriched Mn contents of pyroxenes in some anorthosites suggest that original igneous compositional characteristics have been altered during and/or after crystallization. Processes operative during anorthosite formation may have included some mixing of different melts, trapping of variable amounts of intercumulus liquid, postcrystallization redistribution of elements, or perturbations both during adcumulus growth and subsequent to crystallization by impact events. FeO and MgO contents of the highly calcic plagioclase typical of these anorthosites suggest that the plagioclase-melt distribution coefficients for these elements need to be reassessed.

Journal of Geophysical Research

Petrologic and geophysical nature of serpentinites

Mineralogically, serpentinites consist predominantly of lizardite, clinochrysotile, and antigorite. Recent work has shown that these minerals are not polymorphs. Chrysotile is the only mineral recognized as a synthetic product in experimental studies of the system MgO-SiO 2 -H 2 O. Antigorite seems to be stable at higher temperatures than lizardite or chrysotile. The density of individual serpentine species is dependent on their morphology; the low-density serpentinites (<2.55g/cc) consist predominantly of clino-chrysotile. Seismic velocities and magnetic susceptibilities of serpentinites are related to the degree of serpentinization. The transition of massive serpentinites from ductile to brittle behavior in laboratory experiments at high confining pressures and temperatures above 300°C has been related to dehydration which may provide a mechanism for developing deep-focus earthquakes along Benioff zones. Serpentinite is formed by direct hydration of ultramafic protolith in the crust. The most common ultramafic protoliths are harzburgite, dunite, and Iherzolite. The assemblage generally developed from these is lizardite + chrysotile + brucite + magnetite. In areas of high-grade metamorphism, antigorite is the predominant serpentine mineral. The common, large, alpine-type serpentinized ultramafic masses contain brucite and have MgO/SiO 2 ratios similar to those of their protolith, resulting in volume increase during serpentinization. Metamorphic serpentinites and some highly sheared alpine-type serpentinites have lower MgO/SiO 2 ratios than their protolith, lack brucite, and appear t o have been formed by volume-for-volume replacement with concomitant loss of magnesium or addition of silica. Many large, young masses of peridotite appear to be slabs of oceanic mantle over-thrust onto continental edges. Subsequent sedimentation, serpentinization, and tectonism have greatly modified these original slabs so that their recognition in older orogenic zones is equivocal. The concept of the tectonic evolution of ultramafic rocks from oceanic crust-mantle slabs invading continental margins and being incrementally serpentinized and moved by later tectonic events provides a working hypothesis that allows a better explanation of the many peculiar and varied occurrences of serpentinite. The evidence does not support Hess' suggestion that the third layer of the oceanic crust consists of partly serpentinized mantle peridotite.

Bulletin of the Geological Society of America

Multivariate analyses of Erzgebirge granite and rhyolite composition: Implications for classification of granites and their genetic relations

High-precision major, minor and trace element analyses for 44 elements have been made of 329 Late Variscan granitic and rhyolitic rocks from the Erzgebirge metallogenic province of Germany. The intrusive histories of some of these granites are not completely understood and exposures of rock are not adequate to resolve relationships between what apparently are different plutons. Therefore, it is necessary to turn to chemical analyses to decipher the evolution of the plutons and their relationships. A new classification of Erzgebirge plutons into five major groups of granites, based on petrologic interpretations of geochemical and mineralogical relationships (low-F biotite granites; low-F two-mica granites; high-F, high-P2O5 Li-mica granites; high-F, low-P2O5 Li-mica granites; high-F, low-P2O5 biotite granites) was tested by multivariate techniques. Canonical analyses of major elements, minor elements, trace elements and ratio variables all distinguish the groups with differing amounts of success. Univariate ANOVA's, in combination with forward-stepwise and backward-elimination canonical analyses, were used to select ten variables which were most effective in distinguishing groups. In a biplot, groups form distinct clusters roughly arranged along a quadratic path. Within groups, individual plutons tend to be arranged in patterns possibly reflecting granitic evolution. Canonical functions were used to classify samples of rhyolites of unknown association into the five groups. Another canonical analysis was based on ten elements traditionally used in petrology and which were important in the new classification of granites. Their biplot pattern is similar to that from statistically chosen variables but less effective at distinguishing the five groups of granites. This study shows that multivariate statistical techniques can provide significant insight into problems of granitic petrogenesis and may be superior to conventional procedures for petrological interpretation.

Computers & Geosciences