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At least 1,513 records · Page 84Linked to original sources

USGS1997

The variable role of slab-derived fluids in the generation of a suite of primitive calc-alkaline lavas from the Southernmost Cascades, California

The compositional continuum observed in primitive calc-alkaline lavas erupted from small volcanoes across the southernmost Cascade arc is produced by the introduction of a variable proportion of slab-derived fluid into the superjacent peridotite layer of the mantle wedge. Magmas derived from fluid-rich sources are erupted primarily in the forearc and are characterized by Sr and Pb enrichment (primitive mantle-normalized Sr/P > 5.5), depletions of Ta and Nb, low incompatible-element abundances, and MORB-like Sr and Pb isotopic ratios. Magmas derived from fluid-poor sources are erupted primarily in the arc axis and behind the arc, and are characterized by weak enrichment in Sr [1.0 < (Sr/P)N < 1.3], weak depletions in Ta and Nb, higher incompatible-element abundances, and OIB-like Sr, Nd, and Pb isotopic ratios. Fluxing the mantle wedge above the subducting slab with H2O-rich fluid stabilizes amphibole and enriches the wedge peridotites in incompatible elements, particularly unradiogenic Sr and Pb. The hydrated amphibole-bearing portion of the mantle wedge is downdragged beneath the forearc, where its solidus is exceeded, yielding melts that are enriched in Sr and Pb, and depleted in Ta and Nb (reflecting both high Sr and Pb relative to Ta and Nb in the fluid, and the greater compatibility of Ta and Nb in amphibole compared to other silicate phases in the wedge). A steady decrease of the fluid-contributed geochemical signature away from the trench is produced by the progressive dehydration of the downdragged portion of the mantle wedge with depth, resulting from melt extraction and increased temperature at the slab-wedge interface. Inverse correlation between incompatible-element abundances and the size of the fluid-contributed geochemical signature is generated by melting of more depleted peridotites, rather than by significant differences in the degree of melting. High-(Sr/P)N lavas of the forearc are generated by melting of a MORB-source-like peridotite that has been fluxed with a greater proportion of slab-derived fluid, and low (Sr/P)N lavas of the arc axis are produced by melting of an OIB-source-like peridotite in the presence of a smaller proportion of slab-derived fluid. This study documents the control that a slab-derived fluid can have on incompatible element and isotopic systematics of arc magmas by 1) the addition of incompatible elements to the wedge, 2) the stabilization of hydrous phases in the wedge, and 3) the lowering of peridotite solidi.

Canadian Mineralogist↗

USGS1998

The provenance and chemical variation of sandstones associated with the Mid-continent Rift System, U.S.A.

Sandstones along the northern portion of the Precambrian Mid-continent Rift System (MRS) have been petrographically and chemically analyzed for major elements and a variety of trace elements, including the REE. After the initial extrusion of the abundant basalts along the MRS, dominantly volcaniclastic sandstones of the Oronto Group were deposited. These volcaniclastic sandstones are covered by quartzose and subarkosic sandstones of the Bayfield Group. Thus the sandstones of the Oronto Group were derived from previously extruded basalts, whereas, the sandstones of the Bayfield Group were derived from Precambrian granitic gneisses located on the rift flanks. The chemical variation of these sandstones closely reflects the changing detrital modes with time. The elemental composition of the sandstones confirms the source lithologies suggested by the mineralogy and clasts. The Oronto Group sandstones contain lower ratios of elements concentrated in silicic source rocks (La or Th) relative to elements concentrated in basic source rocks (Co, Cr, or Sc) than the Bayfield Group. Also, the average size of the negative Eu anomaly of the sandstones of the Oronto Group is significantly less (Eu/Eu* mean ?? standard deviation = 0.79 ?? 0.13) than that of the Bayfield Group (mean + standard deviation = 0.57 ?? 0.09), also suggesting a more basic source for the former than the latter. Mixing models of elemental ratios give added insight as to the evolution of the rift. These models suggest that the volcanistic sandstones of the lower portion of the Oronto Group are derived from about 80 to 90 percent basalt and 10 to 20 percent granitoids. The rest of the Oronto Group and the lower to middle portion of the Bayfield Group could have formed by mixing of about 30 to 60 percent basalt and 40 to 70 percent granitoids. The upper portion of the Bayfield Group is likely derived from 80 to 100 percent granitoids and zero to 20 percent basalt.

European Journal of Mineralogy↗

USGS2000

Formation evaluation of gas hydrate-bearing marine sediments on the Blake Ridge with downhole geochemical log measurements

The analyses of downhole log data from Ocean Drilling Program (ODP) boreholes on the Blake Ridge at Sites 994, 995, and 997 indicate that the Schlumberger geochemical logging tool (GLT) may yield useful gas hydrate reservoir data. In neutron spectroscopy downhole logging, each element has a characteristic gamma ray that is emitted from a given neutron-element interaction. Specific elements can be identified by their characteristic gamma-ray signature, with the intensity of emission related to the atomic elemental concentration. By combining elemental yields from neutron spectroscopy logs, reservoir parameters including porosities, lithologies, formation fluid salinities, and hydrocarbon saturations (including gas hydrate) can be calculated. Carbon and oxygen elemental data from the GLT was used to determine gas hydrate saturations at all three sites (Sites 994, 995, and 997) drilled on the Blake Ridge during Leg 164. Detailed analyses of the carbon and oxygen content of various sediments and formation fluids were used to construct specialized carbon/oxygen ratio (COR) fan charts for a series of hypothetical gas hydrate accumulations. For more complex geologic systems, a modified version of the standard three-component COR hydrocarbon saturation equation was developed and used to calculate gas hydrate saturations on the Blake Ridge. The COR-calculated gas hydrate saturations (ranging from about 2% to 14% bulk volume gas hydrate) from the Blake Ridge compare favorably to the gas hydrate saturations derived from electrical resistivity log measurements.

Conference Paper↗

USGS2014

Multi-temporal mapping of a large, slow-moving earth flow for kinematic interpretation

Periodic movement of large, thick landslides on discrete basal surfaces produces modifications of the topographic surface, creates faults and folds, and influences the locations of springs, ponds, and streams (Baum, et al., 1993; Coe et al., 2009). The geometry of the basal-slip surface, which can be controlled by geological structures (e.g., fold axes, faults, etc.; Revellino et al., 2010; Grelle et al., 2011), and spatial variation in the rate of displacement, are responsible for differential deformation and kinematic segmentation of the landslide body. Thus, large landslides are often composed of several distinct kinematic elements. Each element represents a discrete kinematic domain within the main landslide that is broadly characterized by stretching (extension) of the upper part of the landslide and shortening (compression) near the landslide toe (Baum and Fleming, 1991; Guerriero et al., in review). On the basis of this knowledge, we used photo interpretive and GPS field mapping methods to map structures on the surface of the Montaguto earth flow in the Apennine Mountains of southern Italy at a scale of 1:6,000. (Guerriero et al., 2013a; Fig.1). The earth flow has been periodically active since at least 1954. The most extensive and destructive period of activity began on April 26, 2006, when an estimated 6 million m3 of material mobilized, covering and closing Italian National Road SS90, and damaging residential structures (Guerriero et al., 2013b). Our maps show the distribution and evolution of normal faults, thrust faults, strike-slip faults, flank ridges, and hydrological features at nine different dates (October, 1954; June, 1976; June, 1991; June, 2003; June, 2005; May, 2006; October, 2007; July, 2009; and March , 2010) between 1954 and 2010. Within the earth flow we recognized several kinematic elements and associated structures (Fig.2a). Within each kinematic element (e.g. the earth flow neck; Fig.2b), the flow velocity was highest in the middle, and lowest in the upper and lower parts. As the velocity of movement initiated and increased, stretching of the earth flow body induced the formation of normal faults. Conversely, decreasing velocity and shortening of the earth flow induced the formation of thrust faults. A zone with relatively few structures, bounded by strike-slip faults, was located between stretching and shortening areas. These kinematic elements indicate that the overall earth flow was actually composed of numerous linked internal earth flows, with each internal flow having a distinct pattern of structures representative of stretching and shortening (Guerriero et al., in review). These observations indicated that the spatial variation in movement velocity associated with each internal earth flow, mimicked the pattern of movement for the overall earth flow. That is, the earth flow displayed a self-similar pattern at different scales. Furthermore, the presence of other structures such as back-tilted surfaces, flank-ridges, and hydrological elements provide specific information about the shape of the basal topographic surface. Our multi-temporal maps provided a basis for interpretation of the long-term kinematic evolution of the earth flow and the influence of the basal-slip surface on the earth flow movement. Our maps showed that main faults remained stationary through time, despite extensive mobilization and movement of material. This observation indicated that the slip-surface has remained relatively stationary since at least 1954.

Conference Paper↗

USGS1996

Small watershed studies: Analytical approaches for understanding ecosystem response to environmental change

Biogeochemical studies in small watersheds provide an analytical approach to understand how ecosystems respond to natural climatic variations and human-induced environmental change. Small watersheds, usually less than 5 km2, are small enough to permit characterization and understanding of ecosystem processes within relatively simple, homogeneous biological and physical settings; yet they are large enough to incorporate more complex processes and element cycles than can be studied at plot scales. Watersheds comprise discrete hydrochemical environments allowing quantification of hydrologic, element, and energy budgets. Element budgets, or mass balances, can be quantified as the difference between the mass of a solute that enters a watershed in wet and dry deposition and leaves a watershed in streamflow. Element budgets are primary tools used to investigate biogeochemical processes. Monitoring various aspects of element budgets to assess ecosystem health and stability is analogous to measuring the pulse or blood chemistry of a patient. Monitoring streamwater chemistry, basic climate, soil, and biotic variables provide a means to integrate complex biogeochemical processes and evaluate trends in water quality. Small watershed studies provide a scientific basis to develop predictive models of watershed function. Major emphases of small watershed studies include investigation of hydrologic and chemical responses to natural climate variation, anthropogenic stressors, and alternate forest-management practices. The nature and significance of biogeochemical research in small watersheds is reviewed by Moldan and Cerny (1994). The U.S. Geological Survey, U.S. Department of Agriculture Forest Service, and other federal agencies support several long-term small watershed studies to provide insight into a variety of ecosystem processes. Long-term records are essential to distinguish trends resulting from natural climatic variations or other stressors. The following sites, with noted periods of records, are examples of intensively studied forested watersheds in eastern USA supported by federal agencies: ■ Coweeta Hydrologic Laboratory, North Carolina, (1939-present), Swank and Crossley (1988). ■ Hubbard Brook Experimental Forest, New Hampshire, (1956-present), Bormann and Likens (1979). ■ Sleepers River Research Watershed, Vermont, (1958-present), Shanley et al. (1995). ■ Walker Branch Watershed, Tennessee, (1967-present), Johnson and Van Hook (1989). ■ Catoctin Mountains Research Site, Maryland, (1982-present), Rice and Bricker (1995). ■ Catskill Stream Network, New York, (1983- present), Murdoch and Stoddard (1992). ■ Panola Mountain Research Watershed, Georgia, (1985-present), Huntington et al. (1993). Small watershed studies also provide essential baseline information for understanding variations in water quality and element cycling in "pristine" ecosystems that can be used as benchmarks to evaluate anthropogenic impacts and alternate watershed management practices. This paper provides examples of how analytical tools developed through watershed research provide insight into ecosystem processes and can contribute to the management of watershed resources.

Conference Paper↗

USGS1956

Preliminary study of radioactive limonite localities in Colorado, Utah, and Wyoming

Nine radioactive limonite localities of different types were sampled during the spring and fall of 1953 in an effort to establish criteria for differentiating limonite outcrops associated with uranium or thorium deposits from limonite outcrops not associated with such deposits. The samples were analyzed for uranium and thorium by standard chemical methods, for equivalent uranium by the radiometric method, and for a number of common metals by semiquantitative geochemical methods. Correlation coefficients were then calculated for each of the metals with respect to equivalent uranium, and to uranium where present, for all of the samples from each locality. The correlation coefficients may indicate a significant association between uranium or thorium and certain metals. Occurrences of specific that are interpreted as significant very considerably for different uranium localities but are more consistent for the thorium localities. Samples taken from radioactive outcrops in the vicinity of uranium or thorium deposits can be quickly analyzed by geochemical methods for various elements. Correlation coefficients can then be determined for the various elements with respect to uranium or thorium; if any significant correlations are obtained, the elements showing such correlation may be indicators of uranium or thorium. Soil samples of covered areas in the vicinity of the radioactive outcrop may then be analyzed for the indicator elements and any resulting anomalies used as a guide for prospecting where the depth of overburden is too great to allow the use of radiation-detecting instruments. Correlation coefficients of the associated indicator elements, used in conjunction with petrographic evidence, may also be useful in interpreting the origin and paragenesis of radioactive deposits. Changes in color of limonite stains on the outcrop may also be a useful guide to ore in some areas.

Colorado;Utah;Wyoming↗

USGS2017

Relationships between gas field development and the presence and abundance of pygmy rabbits in southwestern Wyoming

More than 5957 km 2 in southwestern Wyoming is currently covered by operational gas fields, and further development is projected through 2030. Gas fields fragment landscapes through conversion of native vegetation to roads, well pads, pipeline corridors, and other infrastructure elements. The sagebrush steppe landscape where most of this development is occurring harbors 24 sagebrush-associated species of greatest conservation need, but the effects of gas energy development on most of these species are unknown. Pygmy rabbits ( Brachylagus idahoensis ) are one such species. In 2011, we began collecting three years of survey data to examine the relationship between gas field development density and pygmy rabbit site occupancy patterns on four major Wyoming gas fields (Continental Divide–Creston–Blue Gap, Jonah, Moxa Arch, Pinedale Anticline Project Area). We surveyed 120 plots across four gas fields, with plots distributed across the density gradient of gas well pads on each field. In a 1 km radius around the center of each plot, we measured the area covered by each of 10 gas field infrastructure elements and by shrub cover using 2012 National Agriculture Imagery Program imagery. We then modeled the relationship between gas field elements, pygmy rabbit presence, and two indices of pygmy rabbit abundance. Gas field infrastructure elements—specifically buried utility corridors and a complex of gas well pads, adjacent disturbed areas, and well pad access roads—were negatively correlated with pygmy rabbit presence and abundance indices, with sharp declines apparent after approximately 2% of the area consisted of gas field infrastructure. We conclude that pygmy rabbits in southwestern Wyoming may be sensitive to gas field development at levels similar to those observed for greater sage-grouse, and may suffer local population declines at lower levels of development than are allowed in existing plans and policies designed to conserve greater sage-grouse by limiting the surface footprint of energy development. Buried utilities, gas well pads, areas adjacent to well pads, and well pad access roads had the strongest negative correlation with pygmy rabbit presence and abundance. Minimizing the surface footprint of these elements may reduce negative impacts of gas energy development on pygmy rabbits.

Wyoming↗

USGS2015

Copahue volcano and its regional magmatic setting

Copahue volcano (Province of Neuquen, Argentina) has produced lavas and strombolian deposits over several 100,000s of years, building a rounded volcano with a 3 km elevation. The products are mainly basaltic andesites, with the 2000–2012 eruptive products the most mafic. The geochemistry of Copahue products is compared with those of the main Andes arc (Llaima, Callaqui, Tolhuaca), the older Caviahue volcano directly east of Copahue, and the back arc volcanics of the Loncopue graben. The Caviahue rocks resemble the main Andes arc suite, whereas the Copahue rocks are characterized by lower Fe and Ti contents and higher incompatible element concentrations. The rocks have negative Nb-Ta anomalies, modest enrichments in radiogenic Sr and Pb isotope ratios and slightly depleted Nd isotope ratios. The combined trace element and isotopic data indicate that Copahue magmas formed in a relatively dry mantle environment, with melting of a subducted sediment residue. The back arc basalts show a wide variation in isotopic composition, have similar water contents as the Copahue magmas and show evidence for a subducted sedimentary component in their source regions. The low 206 Pb/ 204 Pb of some backarc lava flows suggests the presence of a second endmember with an EM1 flavor in its source. The overall magma genesis is explained within the context of a subducted slab with sediment that gradually looses water, water-mobile elements, and then switches to sediment melt extracts deeper down in the subduction zone. With the change in element extraction mechanism with depth comes a depletion and fractionation of the subducted complex that is reflected in the isotope and trace element signatures of the products from the main arc to Copahue to the back arc basalts.

Copahue volcano↗

USGS1992

Geochemical evolution of Jurassic diorites from the Bristol Lake region, California, USA, and the role of assimilation

Late Jurassic dioritic plutons from the Bristol Lake region of the eastern Mojave Desert share several geochemical attributes with high-alumina basalts, continental hawaiite basalts, and high-K are andesites including: high K2O concentrations; high Al2O3 (16-19 weight %); elevated Zr/TiO2; LREE (light-rare-earth-element) enrichment (La/YbCN=6.3-13.3); and high Nb. Pearce element ratio analysis supported by petrographic relations demonstrates that P, Hf, and Zr were conserved during differentiation. Abundances of conserved elements suggest that dioritic plutons from neighboring ranges were derived from similar parental melts. In the most voluminous suite, correlated variations in elemental concentrations and (87Sr/86Sr)i indicate differentiation by fractional crystallization of hornblende and plagioclase combined with assimilation of a component characterized by abundant radiogenic Sr. Levenberg-Marquardt and Monte Carlo techniques were used to obtain optimal solutions to non-linear inverse models for fractional crystallization-assimilation processes. Results show that the assimilated material was chemically analogous to lower crustal mafic granulites and that the mass ratio of contaminant to parental magma was on the order of 0.1. Lack of enrichment in 18O with differentiation is consistent with the model results. Elemental concentrations and O, Sr, and Nd isotopic data point to a hydrous REE-enriched subcontinental lithospheric source similar to that which produced some Cenozoic continental hawaiites from the southern Cordillera. Isotopic compositions of associated granitoids suggest that partial melting of this subcontinental lithosphere may have been an important process in the development of the Late Jurassic plutonic arc of the eastern Mojave Desert. ?? 1992 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↗

USGS2026

The use of fluorite geochemistry and machine learning to identify critical mineral systems

Fluorite (CaF 2 ) is a potential pathfinder to critical mineral and rare earth element (REE) deposits but its application has been limited to a narrow range of mineralization types. I show that fluorite is a robust recorder of mineralization fertility by applying statistical and machine-learning methods to a new global fluorite geochemical database. Distinct median rare earth and trace element patterns are observed among deposit types and genetic environments. Fluorite associated with carbonatites and REE deposits are relatively enriched in Sr and have minimal Eu anomalies. These characteristics define new bivariate discrimination diagrams that correctly identify 78% of carbonatite-related fluorite and 88% of fluorite from REE deposits. Random forest classifiers were developed for a wide range of mineralization types and genetic settings. Trained solely on rare earth element patterns, these models achieve accuracies of 77–79%. Higher classification accuracies (up to 88–96%) are obtained when including elements such as Sr, highlighting the significance of trace elements for optimal fluorite classification. The recognition of diagnostic fluorite compositional fingerprints, particularly in REE-fertile systems, underscores its potential as a pathfinder and indicator for critical mineral exploration in F-bearing environments.

Mineralium Deposita↗

USGS2011

Stoichiometric relationship between suspension-feeding caddisfly (Trichoptera: Brachycentridae) and seston

Organisms must acquire adequate amounts of carbon (C) and nutrients [i.e., nitrogen (N) and phosphorus (P)] from their food to support growth. The growth of organisms can be constrained by consumer-resource elemental imbalances in C:nutrient ratios, especially in aquatic ecosystems. Furthermore, the elemental composition of aquatic organisms can change through ontogeny, which can impose additional challenges to growth (the growth rate hypothesis), terminal body size, and reproductive output. In streams, growth in larval aquatic insects is influenced primarily by food quality and quantity, temperature, and population density. We conducted a field study that tracked the growth of a common suspension-feeding caddisfly ( Brachycentrus occidentalis ) through its ontogeny by comparing the elemental composition (C:N:P) of the organism with its available food supply (suspended particulate organic matter or seston). Larvae and seston were sampled from four streams throughout 1 year. Differences in the growth of larvae among the streams were evident, even though the streams possessed similar thermal regimes. Spatial and temporal differences in the nutrient contents of B. occidentalis and seston were observed, suggesting a consumer-resource elemental imbalance. Lower C:P and N:P ratios in food were positively correlated to larval growth rate, suggesting growth was limited by P. The C, N, and P contents in B. occidentalis ’ body tissue did change throughout ontogeny. C:nutrient ratios varied across sites during larval development; however, inter-site variation decreased substantially as the populations approached pupation. Ultimately, consumer-resource elemental imbalances during the larval stage did not lead to differences in pre-emergent standing stocks across sites.

Hydrobiologia↗

USGS1989

Back-arc with frontal-arc component origin of Triassic Karmutsen basalt, British Columbia, Canada

The largely basaltic, ???4.5-6.2-km-thick, Middle to Upper Triassic Karmutsen Formation is a prominent part of the Wrangellian sequence. Twelve analyses of major and minor elements of representative samples of pillowed and massive basalt flows and sills from Queen Charlotte and Vancouver Islands are ferrotholeiites that show a range of 10.2-3.8% MgO (as normalized, H2O- and CO2-free) and related increases in TiO2 (1.0-2.5%), Zr (43-147 ppm) and Nb (5-16 ppm). Other elemental abundances are not related simply to MgO: distinct groupings are evident in Al2O3, Na2O and Cr, but considerable scatter is present in FeO* (FeO + 0.9Fe2O3) and CaO. Some of the variation is attributed to alteration during low-rank metamorphism or by seawater - including variation of Ba, Rb, Sr and Cu, but high-field-strength elements (Sc, Ti, Y, Zr and Nb) as well as Cr, Ni, Cu and rare-earth elements (REE's) were relatively immobile. REE's show chondrite-normalized patterns ranging from light-REE depleted to moderately light-REE enriched. On eleven discriminant plots these analyses fall largely into or across fields of within-plate basalt (WIP), normal or enriched mid-ocean-ridge tholeiite (MORB) and island-arc tholeiite (IAT). Karmutsen basalts are chemically identical to the stratigraphically equivalent Nikolai Greenstone of southern Alaska and Yukon Territory. These data and the fact that the Karmutsen rests on Sicker Group island-arc rocks of Paleozoic age suggest to us that: 1. (1) the basal arc, after minor carbonate-shale deposition, underwent near-axial back-arc rifting (as, e.g., the Mariana arc rifted at different times); 2. (2) the Karmutsen basalts were erupted along this rift or basin as "arc-rift" tholeiitite; and 3. (3) after subsequent deposition of carbonates and other rocks, and Jurassic magmatism, a large fragment of this basalt-sediment-covered island arc was accreted to North America as Wrangellia. The major- and minor-elemental abundances of Karmutsen basalt is modeled by first mixing primitive arc magma with enriched basaltic liquid derived either from garnet peridotite or metasomatized mantle, followed by fractionation of olivine, pyroxenes, plagioclase and spinel. ?? 1989.

Chemical Geology↗

USGS1983

Geochemistry of diverse basalt types from Loihi Seamount, Hawaii: Petrogenetic implications

The wide variety of basalt types, tholeiitic to basanite, dredged from Loihi Seamount have minor and trace element abundances that are characteristic of subaerial Hawaiian basalts, thereby confirming that Loihi Seamount is a manifestation of the Hawaiian “hot spot”. Within the Loihi sample suite there are well-defined positive correlations among abundances of highly incompatible elements (P, K, Rb, Ba, Nb, light REE and Ta) and moderately incompatible elements (Sr, Ti, Zr and Hf) and between MgO, Ni and Cr. However, within the Loihi suite abundance ratios of geochemically similar elements (Zr/Hf, Nb/Ta and La/Ce) vary by factors of 1.2–1.5 and abundance ratios of highly incompatible elements such as P/Ce, P/Th, K/Rb, Ba/Th and La/Nb vary by factors of 1.2–2.5. These abundance ratios are not readily changed by different degrees of fractionation and melting. Therefore, we conclude that these samples are not genetically related by different degrees of melting of a compositionally homogeneous source.

Hawaii↗

USGS1995

A mass proportion method for calculating melting reactions and application to melting of model upper mantle lherzolite

We present a method for calculating quantitative melting reactions in systems with multiple solid solutions that accounts for changes in the mass proportions of phases between two points at different temperatures along a melting curve. This method can be applied to any data set that defines the phase proportions along a melting curve. The method yields the net change in mass proportion of all phases for the chosen melting interval, and gives an average reaction for the melting path. Instantaneous melting reactions can be approximated closely by choosing sufficiently small melting intervals. As an application of the method, reactions for melting of model upper mantle peridotite are calculated using data from the system CaO-MgO-Al 2 O 3 -SiO 2 -Na 2 O (CMASN) over the pressure interval 0.7 – 3.5 GPa. Throughout almost this entire pressure range, melting of model lherzolite involves the crystallization of one or more solid phases, and is analogous to melting at a peritectic invariant point. In addition, we show that melting reactions for small melting intervals (< 5%) along the solidus of mantle peridotite are significantly different from those calculated for large melting intervals. For large melting intervals (> 10%), reaction stoichiometries calculated in CMASN are usually in good agreement with those available for melting of natural peridotite. The coefficients of melting reactions calculated from this method can be used in equations that describe the behavior of trace elements during melting. We compare results from near-fractional melting models using (1) melting reactions and rock modes from CMASN, and (2) constant reactions representative of those used in the literature. In modeling trace element abundances in melt, significant differences arise for some elements at low degrees of melting (< 10%). In modeling element abundances in the residue, differences increase with increase in degree of melting. Reactions calculated along the model lherzolite solidus in CMASN are the only ones available at present for small degrees of melting so we recommend them for accurate trace element modeling of natural lherzolite.

Earth and Planetary Science Letters↗

USGS1959

Composition of monazites from pegmatites in eastern Minas Gerais, Brazil

Two zoned pegmatites in south-eastern Minas Gerais were sampled in detail for their content of monazite and xenotime and the monazite was analysed for certain of the rare-earth elements and thorium. The ratio of xenotime to monazite increases in both pegmatites from the wall toward the quartz core. The content of the less basic rare-earth elements and of thorium in monazite rises in the same direction. These variation trends suggest that during the crystallization of these pegmatites there was a fractionation of the elements leading to a more or less steady enrichment of the less basic rare-earth elements and of thorium in the residual fluids. One mode of explaining these observed effects postulates that the rare-earth elements and thorium were present in pegmatitic fluids as co-ordination complexes rather than as simple cations.

Minas Gerais↗

USGS1968

Variation of Nb-Ta, Zr-Hf, Th-U and K-Cs in two diabase-granophyre suites

Concentrations of Nb, Ta, Zr, Hf, Th, U and Cs have been determined in samples of igneous rocks representing the diabase-granophyre suites from Dillsburg, Pennsylvania, and Great Lake, Tasmania. Niobium and tantalum have a three to fourfold increase with differentiation in each of the suites. The chilled margin of the Great Lake intrusion contains half the niobium and tantalum content (5.3 ppm and 0.4 ppm, respectively) of the chilled basalt from Dillsburg (10 ppm and 0.9 ppm, respectively). The twofold difference between the suites is correlated with differences in their titanium content. The average Nb Ta "> NbTa ratios for each suite are similar: 13.5 for the Great Lake suite, and 14.4 for the Dillsburg suite. The zirconium content of the two suites is essentially the same and increases from 50 to 60 ppm in the chilled margins to 240–300 ppm in the granophyres. Hafnium is low in the early formed rocks (0.5 –1.5 ppm and achieves a maximum in the granophyres (5–8 ppm). The Zr Hf "> ZrHf ratio decreases from 68 to 33 with progressive differentiation. In the Dillsburg suite thorium and uranium increase from 2.6 ppm and 0.6 ppm, respectively, in the chilled samples to 11.8 ppm and 3.1 ppm in the granophyres. The chilled margin of the Great Lake suite contains 3.2 ppm thorium and 9.8 ppm uranium; the granophyre contains 11.2 ppm thorium and 2.8 ppm uranium. The average Th U "> ThU ratios of the Dillsburg and Great Lake suites are nearly the same—4.1 and 4.4, respectively. Within each suite the Th U "> ThU ratio remains quite constant. Cesium and the K Cs "> KCs ratio do not vary systematically in the Dillsburg suite possibly because of redistribution or loss of cesium by complex geologic processes. Except for the chilled margin of the Great Lake suite, the variation of Cs and the K Cs "> KCs ratio are in accord with theoretical considerations. Cesium increases from about 0.6 ppm in the lower zone to 3.5 ppm in the granophyre; the K Cs "> KCs ratio varies from 10 × 10 3 in the lower zone to 6 × 10 3 in the granophyre. A comparison of the abundance of some of these elements is made with those reported on oceanic tholeiites from the Atlantic and Pacific oceans. Trace elements with large ionic radii (Th, U, Cs) are present in significantly greater concentrations in the two continental tholeiitic series than in the oceanic tholeiites. However, this does not seem to be true for lithophilic elements of smaller ionic radii (Zr and Nb). These trace element distribution patterns, when considered with other minor element and isotopic studies, indicate that 1. crustal contamination does not entirely account for differences between continental and oceanic tholeiites, and 2. the oceanic tholeiites do not necessarily delimit the geochemical characteristics of the mantle.

Geochimica et Cosmochimica Acta↗

USGS1987

Compositional evidence regarding the origins of rims on Semarkona chondrules

The compositions of the interiors and abraded surfaces of 7 chondrules from Semarkona (LL3.0) were measured by neutron activation analysis. For nonvolatile elements, the lithophile and siderophile element abundance patterns in the surfaces are generally similar to those in the corresponding interiors. Siderophile and chalcophile concentrations are much higher in the surfaces, whereas lithophile concentrations are similar in both fractions. Most of the similarities in lithophile patterns and some of the similarities in siderophile patterns between surfaces and interiors may reflect incomplete separation of the fractions in the laboratory, but for 3 or 4 chondrules the siderophile resemblance is inherent, implying that the surface and interior metal formed from a single precursor assemblage. Metal and sulfide-rich chondrule rims probably formed when droplets of these phases that migrated to the chondrule surface during melting were reheated and incorporated into matrix-like material that had accreted onto the surface. The moderately-volatile to volatile elements K, As and Zn tend to be enriched in the surfaces compared with other elements of similar mineral affinity; both enrichments and depletions are observed for other moderately volatile elements. A small fraction of chondrules experienced fractional evaporation while they were molten.

Geochimica et Cosmochimica Acta↗