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At least 145 records · Page 8Linked to original sources
USGS1970

Water content of basalt erupted on the ocean floor

Deep sea pillow basalts dredged from the ocean floor show that vesicularity changes with composition as well as with depth. Alkalic basalts are more vesicular than tholeiitic basalts erupted at the same depth. The vesicularity data, when related to experimentally determined solubility of water in basalt, indicate that K-poor oceanic tholeiites originally contained about 0.25 percent water, Hawaiian tholeiites of intermediate K-content, about 0.5 percent water, and alkali-rich basalts, about 0.9 percent water. Analyses of fresh basalt pillows show a systematic increase of H 2 O + as the rocks become more alkalic. K-poor oceanic tholeiites contain 0.06–0.42 percent H 2 O + , Hawaiian tholeiites, 0.31–0.60 percent H 2 O + , and alkali rich basalts 0.49–0.98 percent H 2 O + . The contents of K 2 O, P 2 O 5 , F, and Cl increase directly with an increase in H 2 O + content such that at 1.0 weight percent H 2 O + , K 2 O is 1.58 percent, P 2 O 5 is 0.55 percent, F is 0.07 percent, and Cl is 0.1 percent. The measured weight percent of deuterium on the rim of one Hawaiian pillow is −6.0 (relative to SMOW); this value, which is similar to other indications of magmatic water, suggests that no appreciable sea water was absorbed by the pillow during or subsequent to eruption on the ocean floor. Concentrations of volatile constituents in the alkali basalt melts relative to tholeiitic melts can be explained by varying degrees of partial melting of mantle material or by fractional crystallization of a magma batch.

Contributions to Mineralogy and Petrology↗
USGS1986

Oxygen isotope compositions of selected laramide-tertiary granitoid stocks in the Colorado Mineral Belt and their bearing on the origin of climax-type granite-molybdenum systems

Quartz phenocrysts from 31 granitoid stocks in the Colorado Mineral Belt yield ??18O values less than 10.4???, with most values between 9.3 and 10.4???. An average magmatic value of about 8.5??? is suggested. The stocks resemble A-type granites; these data support magma genesis by partial melting of previously depleted, fluorine-enriched, lower crustal granulites, followed by extreme differentiation and volatile evolution in the upper crust. Subsolidus interaction of isotopically light water with stocks has reduced most feldspar and whole rock ??18O values. Unaltered samples from Climax-type molybdenumbearing granites, however, show no greater isotopic disturbance than samples from unmineralized stocks. Although meteoric water certainly played a role in post-mineralization alteration, particularly in feldspars, it is not required during high-temperature mineralization processes. We suggest that slightly low ??18O values in some vein and replacement minerals associated with molybdenum mineralization may have resulted from equilibration with isotopically light magmatic water and/or heavy isotope depletion of the ore fluid by precipitation of earlier phases. Accumulation of sufficient quantities of isotopically light magmatic water to produce measured depletions of 18O requires extreme chemical stratification in a large magma reservoir. Upward migration of a highly fractionated, volatile-rich magma into a small apical Climax-type diapir, including large scale transport of silica, alkalis, molybdenum, and other vapor soluble elements, may occur with depression of the solidus temperature and reduction of magma viscosity by fluorine. Climax-type granites may provide examples of 18O depletion in magmatic systems without meteoric water influx. ?? 1986 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1982

The chemical and isotopic record of rock-water interaction in the Sherman Granite, Wyoming and Colorado

Chemical, isotopic, radiographic, and rock-leaching data are combined to describe the effects of rock-water interactions in core samples of petrographically fresh, 1.43 b.y.-old Sherman Granite. The data serve to identify sensitive indicators of incipient alteration and to estimate the degree, pathways, and timing of element mobilization. Unfractured core samples of Sherman Granite are remarkably fresh by most chemical or isotopic criteria, but incipient alteration is indicated by the abundance and distribution of uranium and the degree of radioactive equilibration of uranium with its decay products. Uranium abundances which are out of equilibrium with lead decay products indicate remobilization of a portion (3 to 60 percent) of original uranium in late Phanerozoic time. Association of uranium with minor but pervasive secondary alteration products also indicates some remobilization. The amount of apparent uranium mobility in unfractured Sherman Granite (3 to 60 percent) is small compared to the results of similar studies of Archean granites from nearby localities. Chemical and isotopic data evaluated as a function of core-sample depth suggest a uranium migrational pathway involving near-surface leaching and reconcentration at depth. Movement of solutions through the upper 200 ft (60 m) of Sherman Granite is fracture controlled, and brecciated granite shows more obvious petrographic, chemical, and isotopic evidence of alteration and multi-element redistribution. Laboratory experiments using freshly crushed Sherman Granite confirm that uranium is leached in preference to elements such as Si, Mg, Ca, and K, and that leachable uranium is situated close to the solid-liquid interface; perhaps as uranium along grain boundaries, in crystal defects, or on cleavage traces of minerals that exclude uranium from their structure. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1982

Evolution of continental crust and mantle heterogeneity: Evidence from Hf isotopes

We present initial 176Hf/177 Hf ratios for many samples of continental crust 3.7-0.3 Gy old. Results are based chiefly on zircons (1% Hf) and whole rocks: zircons are shown to be reliable carriers of essentially the initial Hf itself when properly chosen on the basis of U-Pb studies. Pre-3.0 Gy gneisses were apparently derived from an unfractionated mantle, but both depleted and undepleted mantle are evident as magma sources from 2.9 Gy to present. This mantle was sampled mainly from major crustal growth episodes 2.8, 1.8 and 0.7 Gy ago, all of which show gross heterogeneity of 176Hf/177Hf in magma sources from ??Hf=0 to +14, or about 60% of the variability of the present mantle. The approximate ??Hf=2??Nd relationship in ancient and modern igneous rocks shows that 176Lu/177Hf fractionates in general twice as much as 147Sm/144Nd in mantle melting processes. This allows an estimation of the relative value of the unknown bulk solid/liquid distribution coefficient for Hf. DLu/DHf=??? 2.3 holds for most mantle source regions. For garnet to be an important residual mantle phase, it must hold Hf strongly in order to preserve Hf-Nd isotopic relationships. The ancient Hf initials are consistent with only a small proportion of recycled older cratons in new continental crust, and with quasi-continuous, episodic growth of the continental crust with time. However, recycling of crust less than 150 My old cannot realistically be detected using Hf initials. The mantle shows clearly the general positive ??Hf resulting from a residual geochemical state at least back to 2.9 Gy ago, and seems to have repeatedly possessed a similar degree of heterogeneity, rather than a continuously-developing depletion. This is consistent with a complex dynamic disequilibrium model for the creation, maintenance and destruction of heterogeneity in the mantle. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1988

Origin of metaluminous and alkaline volcanic rocks of the Latir volcanic field, northern Rio Grande rift, New Mexico

Volcanic rocks of the Latir volcanic field evolved in an open system by crystal fractionation, magma mixing, and crustal assimilation. Early high-SiO2 rhyolites (28.5 Ma) fractionated from intermediate compositionmagmas that did not reach the surface. Most precaldera lavas have intermediate-compositions, from olivine basaltic-andesite (53% SiO2) to quartz latite (67% SiO2). The precaldera intermediate-composition lavas have anomalously high Ni and MgO contents and reversely zoned hornblende and augite phenocrysts, indicating mixing between primitive basalts and fractionated magmas. Isotopic data indicate that all of the intermediate-composition rocks studied contain large crustal components, although xenocrysts are found only in one unit. Inception of alkaline magmatism (alkalic dacite to high-SiO2 peralkaline rhyolite) correlates with, initiation of regional extension approximately 26 Ma ago. The Questa caldera formed 26.5 Ma ago upon eruption of the >500 km3 high-SiO2 peralkaline Amalia Tuff. Phenocryst compositions preserved in the cogenetic peralkaline granite suggest that the Amalia Tuff magma initially formed from a trace element-enriched, high-alkali metaluminous magma; isotopic data suggest that the parental magmas contain a large crustal component. Degassing of water- and halogen-rich alkali basalts may have provided sufficient volatile transport of alkalis and other elements into the overlying silicic magma chamber to drive the Amalia Tuff magma to peralkaline compositions. Trace element variations within the Amalia Tuff itself may be explained solely by 75% crystal fractionation of the observed phenocrysts. Crystal settling, however, is inconsistent with mineralogical variations in the tuff, and crystallization is thought to have occurred at a level below that tapped by the eruption. Spatially associated Miocene (15-11 Ma) lavas did not assimilate large amounts of crust or mix with primitive basaltic magmas. Both mixing and crustal assimilation processes appear to require development of relatively large magma chambers in the crust that are sustained by large basalt fluxes from the mantle. The lack of extensive crustal contamination and mixing in the Miocene lavas may be related to a decreased basalt flux or initiation of blockfaulting that prevented pooling of basaltic magma in the crust. ?? 1988 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1980

A generalized garnet-forming reaction for metaigneous rocks in the Adirondacks

A generalized reaction is presented to account for garnet formation in a variety of Adirondack metaigneous rocks. This reaction, which is the sum of five partial reactions written in aluminum-fixed frames of reference, is given by: 4(y+1+w)Anorthite+4 k(y+1+2 w)Olivine +4(1-k)(y+1+2 w)Fe-oxide+(8(y+1) -4 k(y+1+2 w))Orthopyroxene = 2(y+1)Garnet +2(y+1+2 w)Clinopyroxene+4 wSpinel where y is a function of plagioclase composition, k refers to the relative amounts of olivine and Fe-oxide participating in the reaction, and w is a measure of silicon mobility. When mass balanced for Mg and Fe, this reaction is found to be consistent with analyzed mineral compositions in a wide range of Adirondack metaigneous rocks. The reaction applies equally well whether the garnets were formed directly from the rectants given above or went through an intermadiate stage involving the formation of spinel, orthopyroxene, and clinopyroxene. The actual reactions which have produced garnet in both undersaturated and quartz-bearing rocks are special cases of the above general reaction. The most important special cases appear to be those in which the reactants include either olivine alone (k=1) or Fe-oxide alone (k=0). Silicon is relatively immobile (w =2) in olivine bearing, magnesium-rich rocks (k???1), and this correlates with the increased intensity in spinel clouding of plagioclase in these rocks. Silicon mobility apparently increases in the more iron-rich rocks, which also tend to contain clear or lightly clouded plagioclase. In all the rocks studied the most common composition of metamorphic plagioclase is close to An33 (i.e., y=1). Plagioclase of lower anorthite content may be too sodic to participate in garnet formation at the P-T conditions involved. ?? 1980 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1983

Carbonatite tuffs in the Laetolil Beds of Tanzania and the Kaiserstuhl in Germany

Carbonatite lava and tephra are now well known. The only modern eruptive carbonatites, from Oldoinyo Lengai, Tanzania, are of alkali carbonatite, whereas all of the pre-modern examples are of calcite or dolomite. Chemical and stable isotope analyses were made of separate phases of Pliocene carbonatite tuffs of the Laetolil Beds in Tanzania and of Miocene carbonatite tuffs of the Kaiserstuhl in Germany in order to understand the reasons for this major difference. The Laetolil Beds contain numerous carbonatite and melilitite-carbonatite tuffs. It is proposed that the carbonatite ash was originally of alkali carbonate composition and that the alkali component was dissolved, leaving a residuum of calcium carbonate. The least recrystallized melilitite-carbonatite tuff contains early-deposited calcite cement and calcite pseudomorphs after nyerereite (?) that have contents of strontium and barium and ??18O and ??13C values suggestive of incomplete chemical and isotopic exchange during alteration and replacement of alkali carbonatite ash. Carbonatite tuffs of the Kaiserstuhl contain globules composed of calcite phenocrysts and microphenocrysts in a groundmass of calcite with a small amount of clay, apatite, and magnetite. The SrO contents of phenocrysts, microphenocrysts, and groundmass calcite average 0.90, 1.42, and 0.59 percent, respectively. The average ??18O and ??13C values of globules (+14.3 and -9.0, respectively) fall between those of coarse-grained intrusive Kaiserstuhl carbonatite (avg. +6.6, -5.8) and those of low-temperature calcite cement in the carbonatite tuffs (+21.8, -14.9). The phenocrysts and microphenocrysts are primary magmatic calcite, but several features indicate that the groundmass has been recrystallized and altered in contact with meteoric water, resulting in weathering of silicate to clay, leaching of strontium, and isotopic exchange. The weight of evidence favors an original high content of alkali carbonatite in the groundmass, with recrystallization following leaching of the alkalies. ?? 1983 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1988

Compositional evolution of the zoned calcalkaline magma chamber of Mount Mazama, Crater Lake, Oregon

The climactic eruption of Mount Mazama has long been recognized as a classic example of rapid eruption of a substantial fraction of a zoned magma body. Increased knowledge of eruptive history and new chemical analyses of ∼350 wholerock and glass samples of the climactic ejecta, preclimactic rhyodacite flows and their inclusions, postcaldera lavas, and lavas of nearby monogenetic vents are used here to infer processes of chemical evolution of this late Pleistocene — Holocene magmatic system. The 6845±50 BP climactic eruption vented ∼50 km 3 of magma to form: (1) rhyodacite fall deposit; (2) welded rhyodacite ignimbrite; and (3) lithic breccia and zoned ignimbrite, these during collapse of Crater Lake caldera. Climactic ejecta were dominantly homogeneous rhyodacite (70.4±0.3% SiO 2 ), followed by subordinate andesite and cumulate scoriae (48–61% SiO 2 ). The gap in wholerock composition reflects mainly a step in crystal content because glass compositions are virtually continuous. Two types of scoriae are distinguished by different LREE, Rb, Th, and Zr, but principally by a twofold contrast in Sr content: High-Sr (HSr) and low-Sr (LSr) scoriae. HSr scoriae were erupted first. Trace element abundances indicate that HSr and LSr scoriae had different calcalkaline andesite parents; basalt was parental to some mafic cumulate scoriae. Parental magma compositions reconstructed from scoria wholerock and glass data are similar to those of inclusions in preclimactic rhyodacites and of aphyric lavas of nearby monogenetic vents. Preclimactic rhyodacite flows and their magmatic inclusions give insight into evolution of the climactic chamber. Evolved rhyodacite flows containing LSr andesite inclusions were emplaced between ∼30000 and ∼25000 BP. At 7015±45 BP, the Llao Rock vent produced a zoned rhyodacite pumice fall, then rhyodacite lava with HSr andesite inclusions. The Cleetwood rhyodacite flow, emplaced immediately before the climactic eruption and compositionally identical to climactic rhyodacite (volatile-free), contains different HSr inclusions from Llao Rock. The change from LSr to HSr inclusions indicates replenishment of the chamber with andesite magma, perhaps several times, in the latest Pleistocene to early Holocene. Modeling calculations and wholerock-glass relations suggest than: (1) magmas were derived mainly by crystallization differentiation of andesite liquid; (2) evolved preclimactic rhyodacite probably was derived from LSr andesite; (3) rhyodacites contain a minor component of partial melt from wall rocks, and (4) climactic and compositionally similar rhyodacites probably formed by mixing of evolved rhyodacite with HSr derivative liquid(s) after replenishment of the chamber with HSr andesite magma. Density considerations permit a model for growth and evolution of the chamber in which andesite recharge magma ponded repeatedly between cumulates and rhyodacite magma. Convective cooling of this andesite resulted in rapid crystallization and upward escape of buoyant derivative liquid which mixed with overlying, convecting rhyodacite. The evolved rhyodacites were erupted early in the chamber's history and(or) near its margins. Postcaldera andesite lavas may be hybrids composed of LSr cumulates mixed with remnant climactic rhyodacite. Younger postcaldera rhyodacite probably formed by fractionation of similar andesite and assimilation of partial melts of wallrocks. Uniformity of climactic rhyodacite suggests homogeneous silicic ejecta from other volcanoes resulted from similar replenishment-driven convective mixing. Calcalkaline pluton compositions and their internal zonation can be interpreted in terms of the Mazama system frozen at various times in its history.

Oregon↗
USGS1969

Primitive and contaminated basalts from the Southern Rocky Mountains, U.S.A

Basalts in the Southern Rocky Mountains province have been analyzed to determine if any of them are primitive. Alkali plagioclase xenocrysts armored with calcic plagioclase seem to be the best petrographic indicator of contamination. The next best indicator of contamination is quartz xenocrysts armored with clinopyroxene. On the rocks and the region studied, K 2 O apparently is the only major element with promise of separating primitive basalt from contaminated basalt inasmuch as it constitutes more than 1 % in all the obviously contaminated basalts. K 2 O: lead (> 4 ppm) and thorium (> 2 ppm) contents and Rb/Sr (> 0.035) are the most indicative of the trace elements studied. Using these criteria, three basalt samples are primitive (although one contains 1.7% K 2 O) and are similar in traceelement contents to Hawaiian and Eastern Honshu, Japan, primitive basalts. Contamination causes lead isotope ratios, 206 Pb/ 204 Pb and 208 Pb/ 204 Pb, to become less radiogenic, but it has little or no effect on 87 Sr/ 86 Sr. We interpret the effect on lead isotopes to be due to assimilation either of lower crustal granitic rocks, which contain 5–10 times as much lead as basalt and which have been low in U/Pb and Th/Pb since Precambrian times, or of upper crustal Precambrian or Paleozoic rocks, which have lost much of their radiogenic lead because of heating prior to assimilation. The lack of definite effects on strontium isotopes may be due to the lesser strontium contents of granitic crustal rocks relative to basaltic rocks coupled with lack of a large radiogenic enrichment in the crustal rocks. Lead isotope ratios were found to be less radiogenic in plagioclase separates from an obviously contaminated basalt than in the primitive basalts. The feldspar separate that is rich in sodic plagioclase xenocrysts was found to be similar to the whole-rock composition for 206 Pb/ 204 Pb and 208 Pb/ 204 Pb whereas a more dense fraction probably enriched in more calcic plagioclase phenocrysts is more similar to the primitive basalts in lead isotope ratios. The primitive basalts have: 206 Pb/ 204 Pb ∼ 18.09–18.34, 207 Pb/ 204 Pb ∼ 15.5, 208 Pb/ 204 Pb ∼ 37.6–37.9, 87 Sr/ 86 Sr ∼ 0.704–0.705. In the primitive basalts from the Southern Rocky Mountains the values of 206 Pb/ 204 Pb are similar to values reported by others for Hawaiian and eastern Honshu basalts and abyssal basalts, whereas 208 Pb/ 204 Pb tends to be equal to or a little less radiogenic than those from the oceanic localities. 87 Sr/ 86 Sr appears to be equal to or a little greater than those of the oceanic localities. These 206 Pb/ 204 Pb and 208 Pb/ 204 Pb ratios are distinctly less radiogenic and 87 Sr/ 86 Sr values are about equal to those reported by others for volcanic islands on oceanic ridges and rises.

Colorado↗
USGS1986

The evolution of young silicic lavas at Medicine Lake Volcano, California: Implications for the origin of compositional gaps in calc-alkaline series lavas

At Medicine Lake Volcano, California, the compositional gap between andesite (57-62 wt.% SiO2) and rhyolite (73-74 wt.% SiO2) has been generated by fractional crystallization. Assimilation of silicic crust has also occurred along with fractionation. Two varieties of inclusions found in Holocene rhyolite flows, hornblende gabbros and aphyric andesites, provide information on the crystallization path followed by lavas parental to the rhyolite. The hornblende gabbros are magmatic cumulate residues and their mineral assemblages are preserved evidence of the phases that crystallized from an andesitic precursor lava to generate the rhyolite lavas. The andesitic inclusions represent samples of a parental andesite and record the early part of the differentiation history. Olivine, plagioclase and augite crystallization begins the differentiation history, followed by the disappearance of olivine and augite through reaction with the liquid to form orthopyroxene and amphibole. Further crystallization of the assemblage plagioclase, amphibole, orthopyroxene, magnetite, and apatite from a high-SiO2 andesite leads to rhyolite. This final crystallization process occurs on a cotectic that is nearly horizontal in temperature-composition space. Since a large amount of crystallization occurs over a limited temperature interval, a compositional gap develops between rhyolite and high SiO2 andesite. Liquidus surfaces with shallow slopes in temperature-composition space are characteristic of several late-stage crystallization assemblages in the andesite to rhyolite compositional range. Experimentally produced plagioclase+ amphibole+orthopyroxene+magnetite and plagioclase+ augite+low-Ca pyroxene+magnetite cotectics have liquidus slopes that are nearly flat. At other calc-alkaline volcanic centers crystallization processes involving large compositional changes over small temperature intervals may also be important in the development of bimodal volcanism (i.e. the existence of a composition gap). At Mt. Mazama and Mt. St. Helens, USA and Aso Caldera and Shikotsu, Japan the amphibole-bearing assemblage was important. At Krakatau, Indonesia and Katmai, USA, an augite+orthopyroxene-bearing assemblage was important. In addition to its role in the production of a compositional gap between intermediate and rhyolitic lavas, the crystallization process increases the H2O content of the residual liquid. This rapid increase in residual liquid volatile content which results from the precipitation of a large proportion of crystalline solids may be an important factor among several that lead to explosive silicic eruptions. ?? 1986 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1991

Nd, Sr, and O isotopic variations in metaluminous ash-flow tuffs and related volcanic rocks at the Timber Mountain/Oasis Valley Caldera, Complex, SW Nevada: implications for the origin and evolution of large-volume silicic magma bodies

Nd, Sr and O isotopic data were obtained from silicic ash-flow tuffs and lavas at the Tertiary age (16-9 Ma) Timber (Mountain/Oasis Valley volcanic center (TMOV) in southern Nevada, to assess models for the origin and evolution of the large-volume silicic magma bodies generated in this region. The large-volume (>900 km3), chemically-zoned, Topopah Spring (TS) and Tiva Canyon (TC) members of the Paintbrush Tuff, and the Rainier Mesa (RM) and Ammonia Tanks (AT) members of the younger Timber Mountain Tuff all have internal Nd and Sr isotopic zonations. In each tuff, high-silica rhyolites have lower initial e{open}Nd values (???1 e{open}Nd unit), higher87Sr/86Sr, and lower Nd and Sr contents, than cocrupted trachytes. The TS, TC, and RM members have similar e{open}Nd values for high-silica rhyolites (-11.7 to -11.2) and trachytes (-10.5 to -10.7), but the younger AT member has a higher e{open}Nd for both compositional types (-10.3 and -9.4). Oxygen isotope data confirm that the TC and AT members were derived from low e{open}Nd magmas. The internal Sr and Nd isotopic variations in each tuff are interpreted to be the result of the incorporation of 20-40% (by mass) wall-rock into magmas that were injected into the upper crust. The low e{open}Nd magmas most likely formed via the incorporation of low ??18O, hydrothermally-altered, wall-rock. Small-volume rhyolite lavas and ash-flow tuffs have similar isotopic characteristics to the large-volume ash-flow tuffs, but lavas erupted from extracaldera vents may have interacted with higher ??18O crustal rocks peripheral to the main magma chamber(s). Andesitic lavas from the 13-14 Ma Wahmonie/Salyer volcanic center southeast of the TMOV have low e{open}Nd (-13.2 to -13.8) and are considered on the basis of textural evidence to be mixtures of basaltic composition magmas and large proportions (70-80%) of anatectic crustal melts. A similar process may have occurred early in the magmatic history of the TMOV. The large-volume rhyolites may represent a mature stage of magmatism after repeated injection of basaltic magmas, crustal melting, and volcanism cleared sufficient space in the upper crust for large magma bodies to accumulate and differentiate. The TMOV rhyolites and 0-10 Ma old basalts that erupted in southern Nevada all have similar Nd and Sr isotopic compositions, which suggests that silicic and mafic magmatism at the TMOV were genetically related. The distinctive isotopic compositions of the AT member may reflect temporal changes in the isotopic compositions of basaltic magmas entering the upper crust, possibly as a result of increasing "basification" of a lower crustal magma source by repeated injection of mantle-derived mafic magmas. ?? 1991 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1974

Presentation and interpretation of chemical data for igneous rocks

Arguments are made in favor of using variation diagrams to plot analyses of igneous rocks and their derivatives and modeling differentiation processes by least-squares mixing procedures. These methods permit study of magmatic differentiation and related processes in terms of all of the chemical data available. Data are presented as they are reported by the chemist and specific processes may be modeled and either quantitatively described or rejected as inappropriate or too simple. Examples are given of the differing interpretations that can arise when data are plotted on an AEM ternary vs. the same data on a full set of MgO variation diagrams. Mixing procedures are illustrated with reference to basaltic lavas from the Columbia Plateau.

Idaho, Washington, Oregon↗
USGS1974

Chemistry and mineralogy of garnet pyroxenites from Sabah, Malaysia

Garnet pyroxenites and corundum-garnet amphibolites from the Dent peninsula of eastern Sabah (North Borneo) occur as blocks in a slump breccia deposit of late Miocene age. The earliest formed minerals include pyrope-almandine garnet, tschermakitic augite, pargasite, and rutile. Cumulate textures are present in two of the six specimens studied. The earlier fabric has been extensively brecciated and partly replaced by plagioclase, ilmenite, and a fibrous amphibole. The bulk composition and mineralogy of these rocks are similar to those of garnet pyroxenite lenses within ultramafic rocks. Estimated temperature and pressure for the origin of the Sabah garnet pyroxenites is 850±150° C and 19±4 kbar.

Contributions to Mineralogy and Petrology↗
USGS1989

Boron isotopic composition of tourmaline from massive sulfide deposits and tourmalinites

Boron isotope ratios (11B/10B) have been measured on 60 tourmaline separates from over 40 massive sulfide deposits and tourmalinites from a variety of geologic and tectonic settings. The coverage of these localities is global (5 continents) and includes the giant ore bodies at Kidd Creek and Sullivan (Canada), Broken Hill (Australia), and Ducktown (USA). Overall, the tourmalines display a wide range in ??11B values from -22.8 to +18.3??? Possible controls over the boron isotopic composition of the tourmalines include: 1) composition of the boron source, 2) regional metamorphism, 3) water/rock ratios, 4) seawater entrainment, 5) temperature of formation, and 6) secular variations in seawater ??11B. The most significant control appears to be the composition of the boron source, particularly the nature of footwall lithologies; variations in water/ rock ratios and seawater entrainment are of secondary importance. The boron isotope values seem especially sensitive to the presence of evaporites (marine and non-marine) and carbonates in source rocks to the massive sulfide deposits and tourmalinites. ?? 1989 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1994

Petrogenesis of the highly potassic 1.42 Ga Barrel Spring pluton, southeastern California, with implications for mid-Proterozoic magma genesis in the southwestern USA

Syenites from the Barrel Spring pluton were emplaced in the Early Proterozoic Mojave crustal provine of southeastern California at 1.42 Ga. All rocks, even the most mafic, are highly enriched in incompatible elements (e.g. K 2 O 4–12 wt%, Rb 170–370 ppm, Th 12–120 ppm, La 350–1500xchondrite, La/Yb n 35–100). Elemental compositions require an incompatible element-rich but mafic (or ultramafic) source. Trace element models establish two plausible sources for Barrel Spring magmas: (1) LREE enriched garnet websterite with accessory apatite±rutile (enriched lithospheric mantle), and (2) garnet amphibolite or garnet-hornblende granulite with enriched alkali basalt composition, also with accessory apatite±rutile (mafic lower crust). Nd and Pb isotopic ratios do not distinguish a crust vs mantle source, but eliminate local Mojave province crust as the principal one, and indicate that generation of the enriched source occurred several hundred million years before emplacement of the Barrel Spring pluton. 1.40–1.44 Ga potassic granites are common in southeastern California, suggesting a genetic link between the Barrel Spring pluton and the granites; however, although the same thermal regime was probably responsible for producing both the granitic and syentic magmas, elemental and isotopic compositions preclude a close relationship. Isotopic similarity of the Barrel Spring pluton to 1.40–1.44 Ga granites emplaced in the Central Arizona crustal province to the east may imply that a common component was present in the lithosphere of these generally distinct regions.

California↗
USGS1980

A lead isotope study of mineralization in the Saudi Arabian Shield

New lead isotope data are presented for some late Precambrian and early Paleozoic vein and massive sulfide deposits in the Arabian Shield. Using the Stacey Kramers (1975) model for lead isotope evolution, isochron model ages range between 720 m.y. and 420 m.y. Most of the massive sulfide deposits in the region formed before 680 m.y. ago, during evolution of the shield. Vein type mineralization of higher lead content occurred during the Pan African event about 550 m.y. ago and continued through the Najd period of extensive faulting in the shield that ended about 530 m.y. ago. Late post-tectonic metamorphism may have been responsible for vein deposits that have model ages less than 500 m.y. Alternatively some of these younger model ages may be too low due to the mineralizing fluids acquiring radiogenic lead from appreciably older local crustal rocks at the time of ore formation. The low207Pb/204Pb ratios found for the deposits in the main part of the shield and for those in north-eastern Egypt, indicate that the Arabian craton was formed in an oceanic crustal environment during the late Precambrian. Involvement of older, upper-crustal material in the formation of the ore deposits in this part of the shield is precluded by their low207Pb/204Pb and208Pb/204Pb characteristics. In the eastern part of the shield, east of longitude 44??20???E towards the Al Amar-Idsas fault region, lead data are quite different. They exhibit a linear207Pb/204Pb-206Pb/204Pb relationship together with distinctly higher208Pb/204Pb characteristics. These data imply the existence of lower crustal rocks of early Proterozoic age that apparently have underthrust the shield rocks from the east. If most of the samples we have analyzed from this easterly region were mineralized 530 m.y. ago, then the age of the older continental rocks is 2,100??300 m.y. (2??). The presence of upper crustal rocks, possibly also of early Proterozoic age, is indicated by galena data from Hailan in South Yemen and also from near Muscat in Oman. These data are the first to indicate such old continental material in these regions. ?? 1980 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1983

Distribution of oceanic and continental leads in the Arabian-Nubian Shield

New common lead data for feldspar, whole-rock, and galena samples from the Arabian-Nubian Shield, together with data from previous work, can be divided into two main groups. Group I leads have oceanic (mantle) characteristics, whereas group II leads have incorporated a continental-crustal component of at least early Proterozoic age. The group I leads are found in rocks from the Red Sea Hills of Egypt and the western and southern parts of the Arabian Shield. Group II leads are found in rocks from the northeastern and eastern parts of the Arabian Shield, as well as from the southeastern Shield near Najran. They are also found in rocks to the south in Yemen, to the east in Oman, and to the west at Aswan, Egypt. This distribution of data suggests that the Arabian-Nubian Shield has an oceanic core flanked by rocks that have developed, at least in part, from older continental material. Two mechanisms are suggested by which this older lead component could have been incorporated into the late Proterozoic rocks, and each may have operated in different parts of the Shield. The older lead component either was derived directly from an underlying early Proterozoic basement or was incorporated from subducted pelagic sediments or sediments derived from an adjacent continent. New U-Pb zircon data indicate the presence of an early Proterozoic basement southeast of Jabal Dahul in the eastern Arabian Shield. These data, together with 2,000-Ma-old zircons from the Al Amar fault zone, verify the implication of the common lead data that at least a part of the eastern Arabian Shield has an older continental basement. Because continental margins are particularly favorable locations for development of ore deposits, these findings may have important economic implications, particularly for tin, tungsten, and molybdenum exploration. ?? 1983 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Magmatic inclusions in rhyolites, contaminated basalts, and compositional zonation beneath the Coso volcanic field, California

Basaltic lava flows and high-silica rhyolite domes form the Pleistocene part of the Coso volcanic field in southeastern California. The distribution of vents maps the areal zonation inferred for the upper parts of the Coso magmatic system. Subalkalic basalts (<50% SiO 2 ) were erupted well away from the rhyolite field at any given time. Compositional variation among these basalts can be ascribed to crystal fractionation. Erupted volumes of these basalts decrease with increasing differentiation. Mafic lavas containing up to 58% SiO 2 , erupted adjacent to the rhyolite field, formed by mixing of basaltic and silicic magma. Basaltic magma interacted with crustal rocks to form other SiO 2 -rich mafic lavas erupted near the Sierra Nevada fault zone. Several rhyolite domes in the Coso volcanic field contain sparse andesitic inclusions (55–61% SiO 2 ). Pillow-like forms, intricate commingling and local diffusive mixing of andesite and rhyolite at contacts, concentric vesicle distribution, and crystal morphologies indicative of undercooling show that inclusions were incorporated in their rhyolitic hosts as blobs of magma. Inclusions were probably dispersed throughout small volumes of rhyolitic magma by convective (mechanical) mixing. Inclusion magma was formed by mixing (hybridization) at the interface between basaltic and rhyolitic magmas that coexisted in vertically zoned igneous systems. Relict phenocrysts and the bulk compositions of inclusions suggest that silicic endmembers were less differentiated than erupted high-silica rhyolite. Changes in inferred endmembers of magma mixtures with time suggest that the steepness of chemical gradients near the silicic/mafic interface in the zoned reservoir may have decreased as the system matured, although a high-silica rhyolitic cap persisted. The Coso example is an extreme case of large thermal and compositional contrast between inclusion and host magmas; lesser differences between intermediate composition magmas and inclusions lead to undercooling phenomena that suggest smaller ΔT. Vertical compositional zonation in magma chambers has been documented through study of products of voluminous pyroclastic eruptions. Magmatic inclusions in volcanic rocks provide evidence for compositional zonation and mixing processes in igneous systems when only lava is erupted.

California↗