USGS Science⌕ Search

SEARCH · USGS Science

Results for “Geological Society of America Bulletin”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

1,666 records · Page 45Linked to original sources
USGS2000

Assessment of potential for natural attenuation of chlorinated ethenes and ethanes in ground water at a petrochemical reclamation site, Harris County, Texas

Redox conditions in the Numerous Sand Channels Zone beneath a petrochemical reclamation site in Harris County, Texas, range from sulfate reducing to methanogenic as indicated by the presence of methane in ground water and the range of molecular hydrogen concentrations. Assessment of the potential for reductive dechlorination using BIOCHLOR as a screening tool indicated conditions favoring anaerobic degradation of chlorinated organic compounds in the Numerous Sand Channels Zone. Evidence supporting reductive dechlorination includes apparently biogenic cis -1,2-dichloroethene; an increased ratio of 1,2-dichloroethane to 1,1,2-trichloroethane downgradient from the assumed contaminant source area; ethene and methane concentrations greater than background concentrations within the area of the contaminant plume; and a positive correlation of the ratio of ethene to vinyl chloride as a function of methane concentrations. The body of evidence presented in this report argues for hydrogenolysis of trichloroethene to cis -1,2-dichloroethene; of 1,1,2-trichloroethane to 1,2-dichloroethane; and of vinyl chloride to ethene within the Numerous Sand Channels Zone. Simulations using BIOCHLOR yielded apparent first-order decay constants for reductive dechlorination in the sequence tetrachloroethene trichloroethene cis -1,2-dichloroethene vinyl chloride ethene within the range of literature values reported for each compound and apparent first-order decay constants for reductive dechlorination in the sequence 1,1,2-trichloroethane 1,2-dichloroethane slightly greater than literature values reported for each compound along the upgradient segment of a simulated ground-water flowpath. Except for vinyl chloride, apparent rates of reductive dechlorination for all simulated species show a marked decrease along the downgradient segment of the simulated ground-water flowpath. Evidence for reductive dechlorination of chlorinated ethenes within the Numerous Sand Channels Zone indicates potential for natural attenuation of chlorinated ethenes. Reductive dechlorination of chlorinated ethanes apparently occurs to a lesser extent, indicating relatively less potential for natural attenuation of chlorinated ethanes. Additional data are needed on the concentrations and distribution of chlorinated ethenes and ethanes in individual fine sand intervals of the Numerous Sand Channels Zone. This information, combined with lower minimum reporting levels for future chloroethane analyses, might enable a more complete and quantitative assessment of the potential for natural attenuation at the site.

Texas↗
USGS1996

Hydrogeologic investigation and simulation of ground-water flow in the Upper Floridan Aquifer of north-central Florida and southwestern Georgia and delineation of contributing areas for selected city of Tallahassee, Florida, water-supply wells

A 4-year investigation of the Upper Floridan aquifer and ground-water flow system in Leon County, Florida, and surrounding counties of north-central Florida and southwestern Georgia began in 1990. The purpose of the investigation was to describe the ground-water flow system and to delineate the contributing areas to selected City of Tallahassee, Florida, water-supply wells. The investigation was prompted by the detection of low levels of tetrachloroethylene in ground-water samples collected from several of the city's water-supply wells. Hydrologic data and previous studies indicate that; ground-water flow within the Upper Floridan aquifer can be considered steady-state; the Upper Floridan aquifer is a single water-bearing unit; recharge is from precipitation; and that discharge occurs as spring flow, leakage to rivers, leakage to the Gulf of Mexico, and pumpage. Measured transmissivities of the aquifer ranged from 1,300 ft 2 /d (feet squared per day) to 1,300,000 ft2/d. Steady-state ground-water flow in the Upper Floridan aquifer was simulated using a three-dimensional ground- water flow model. Transmissivities ranging from less than 5,000 ft2/d to greater than 11,000,000 ft 2 /d were required to calibrate to observed conditions. Recharge rates used in the model ranged from 18.0 inches per year in areas where the aquifer was unconfined to less than 2 inches per year in broad areas where the aquifer was confined. Contributing areas to five Tallahassee water-supply wells were simulated by particle- tracking techniques. Particles were seeded in model cells containing pumping wells then tracked backwards in time toward recharge areas. The contributing area for each well was simulated twice, once assuming a porosity of 25 percent and once assuming a porosity of 5 percent. A porosity of 25 percent is considered a reasonable average value for the Upper Floridan aquifer; the 5 percent porosity simulated the movement of ground-water through only solution-enhanced bedding plains and fractures. The contributing areas were generally elliptical in shape, reflecting the influence of the sloping potentiometric surface. The contributing areas delineated for a 5 percent porosity were always much larger than those determined using a 25 percent porosity. The lowest average ground-water velocity computed within a contributing area, using a 25 percent porosity, was 1.0 ft/d (foot per day) and the highest velocity was 1.6 ft/d. The lowest average ground-water velocity, determined using a 5 percent porosity, was 2.4 ft/d and the highest was 7.4 ft/d. The contributing areas for each of the five wells was also determined analytically and compared to the model-derived areas. The upgradient width of the simulated contributing areas were larger than the upgradient width of the analytically determined contributing areas for four of the five wells. The model could more accurately delineate contributing areas because of the ability to simulate wells as partially penetrating and by incorporating complex, three-dimensional aquifer characteristics, which the analytical method could not.

Florida, Georgia↗
USGS2026

Seismic characteristics of the April 2024 eruption of Ruang Volcano, North Sulawesi, Indonesia

The two most recent eruptions of Ruang volcano, in 2002 and 2024, have been large (VEI 4) with very short precursory periods, 3 and 6 days, respectively. Background seismicity at Ruang volcano is generally low with 0–2 volcano-tectonic (VT) earthquakes per day. The 2024 eruptions were preceded by a notable increase in VT earthquakes from 11 to 15 April with a rapid escalation from 16 to 17 April in the form of increased VT swarms, and the appearance of low frequency earthquakes and short bursts of VT drumbeats shortly before the eruption. Similar VT seismic unrest was recorded in March 2015, May 2016, and April 2022, although none of these episodes culminated in an eruption. A comparison of seismic energy release between April 2022 and April 2024 shows distinct differences. In 2024, cumulative seismic energy reached its peak within 5 days, just before the onset of eruption on 17 April. In contrast, during the 2022-episode, energy release followed a more gradual increase over 8 days peaking on 16 April, then declining gradually without leading to eruption. Notably, low frequency (LF) and drumbeat earthquakes were absent in non-eruptive unrest episodes. The transition to proximal LFs in 2024 likely signals pressure fluctuations, intensified magma degassing, and conduit formation, acting as an important precursor to eruption. Additionally, the occurrence of short bursts of drumbeat seismicity likely reflects the onset of the shallow magma ascent and was an important short-term precursor to the eruption. Finally, we examine the potential influence of regional tectonic earthquakes on the escalation of precursory unrest in 2024.

North Sulawesi, Ruang volcano↗
USGS2026

Geophysical architecture and geochronology of the Neoarchean Mentor anorthosite intrusive complex, northwestern Minnesota: Largest anorthosite complex of the Superior Province?

The Neoarchean Mentor anorthosite intrusive complex (MAIC) lies within the Wawa subprovince in northwestern Minnesota, in a region where the Wawa, Quetico, and Wabigoon subprovinces are juxtaposed in close proximity. Archean rocks are entirely concealed, and interpretations are developed from aeromagnetic, gravity, and borehole samples. The MAIC includes both anorthosite (dense, weakly magnetized) and oxide-rich gabbro (strongly magnetized) lithologies. Anorthosite is coarse-grained to megacrystic, intensely altered, and locally brecciated. Pervasive epidote alteration enhanced the density of the anorthosite via introduction of higher-density mineral assemblages, explaining why the MAIC produces a significant gravity high. Oxide-rich gabbro forms a border phase of the MAIC and has potential for vanadium, chromium, and titanium mineralization, and produces a strong aeromagnetic high. The MAIC is interpreted to extend over an area of 640 km 2 , making it the largest known anorthosite complex of the Superior Province, as measured by preserved areal extent. Modeling indicates the MAIC extends more than 6 km into the subsurface. A new Pb–Pb zircon age of 2737.2 ± 4.5 Ma is interpretated as the crystallization age of anorthosite within the MAIC, showing that the MAIC formed well before the ca. 2690 Ma Shebandowanian orogeny, and raising new questions about correlations with other parts of the Wawa subprovince. A low-density batholith, here informally called the Fertile batholith, is interpreted to intrude the southern part of the MAIC. A new Pb–Pb zircon age of 2701.1 ± 6 Ma is interpreted as the magmatic age of the Fertile batholith.

Minnesota↗
USGS2026

Sedimentological and geochemical characterization of lacustrine deposits of the Babouri-Figuil basin, northern Cameroon: Implications for source rocks distribution and petroleum exploration

The West and Central African Rift System (WCARS) refers to the series of Cretaceous rift basins where commercial hydrocarbon accumulations have been discovered. Some of the WCARS frontier basins are currently being investigated to increase our understanding of these basins in light of new commercial discoveries. The present study was performed in the Babouri-Figuil Basin (BFB), which is genetically related to the WCARS and constitutes an area of interest in terms of petroleum prospecting, where the distribution of petroleum source rocks and potential targets for petroleum exploration across the entire basin is poorly understood. For the current study, an integrated facies analysis along with organic and inorganic geochemical techniques were applied to the basin's Cretaceous deposits with the aim of reconstructing the paleodepositional environment, assessing factors that triggered the input of organic matter, and providing a spatial overview of the organic matter accumulation in the basin based on outcrop samples. An alluvial fan-lacustrine-braided river system is inferred from the facies analysis of the stratigraphic sequence consisting of conglomerate, sandstone, siltstone, limestone, marlstone, and claystone. Bulk analysis of organic matter reveals that black shale and massive claystone are the main prospective petroleum source rocks in the basin. Inorganic geochemical analyses reveal the influence of anoxic conditions, moderate to high primary productivity, and low terrigenous inputs in organic matter enrichment. The formations rich in organic matter are predominantly concentrated in the western and eastern parts of the basin which may represent areas with depressions, characterized by high accommodation space. In terms of the regional context of the WCARS rift basins, typical hydrocarbon exploration in the BFB may target basal-conglomerate, sandstone beds situated directly above or/and interbedded with the Lower Cretaceous source rocks, and the Upper Cretaceous sandstone beds. Basement rocks (granite, granodiorite, and gneisses) and oil shale deposits may represent potential unconventional hydrocarbon exploration. The current integrated study provides an insight that should guide future hydrocarbon exploration campaigns in the basin.

Babouri-Figuil basin↗
USGS2025

3D viscoelastic models of slip-deficit rate along the Cascadia subduction zone

Interseismic deformation in the Pacific Northwest is constrained by the horizontal crustal velocity field derived from the Global Positioning System (GPS) in addition to vertical rates derived from GPS, leveling, and tide gauge measurements. Such measurements were folded in to deformation models of fault slip rates as part of the 2023 National Seismic Hazard Model (NSHM) update. Here I build upon one of the contributing models, the viscoelastic earthquake-cycle model of Pollitz [2022]. This model permits inclusion of effects of time-dependent viscoelastic relaxation within earthquake cycles (i.e., ‘ghost transients’) and laterally variable elastic and/or ductile material properties. I lever-age these capabilities to incorporate the Cascadia megathrust into Western U.S.-wide deformation models in which crustal fault slip rates are estimated simultaneously with slip deficit rates along the interplate boundary between the descending Juan de Fuca plate and North American plate. This effort includes construction of a margin-wide model of viscoelastic structure founded on the Slab 2.0 model and probes different models of the ductile properties of the surrounding oceanic asthenosphere, continental lower crust, and mantle asthenosphere. This results in new estimates of the distribution of slip deficit rate along the ∼ 1000 km long margin, highlights the importance of correcting for glacial-isostatic adjustment effects, and permits assessment of sensitivity of results to assumed ductile properties.

California, Oregon, Washington↗
USGS1976

Effect of deicing chemicals on the hydrologic environment in Massachusetts; evaluation of surface-water data collection

The objective of this study is to develop predictive relationships that can be used to describe the impact of highway deicing salts on the hydrologic environment. A method, presented in an earlier report, for estimating yearly mean chloride concentrations from estimated or actual runoff and salt-application data was applied to the period 1971 through1974 and the results compared with yearly mean chloride concentrations computed from records of specific conductance. Estimates were found to be from minus 63 percent to plus 56 percent in error when the error was expressed as the difference between estimated and computed values as a percentage of the computed values. Chloride concentrations used in this study are computed from specific conductance/chloride concentration relationships and records of specific conductance. Preliminary results from graphic analyses and least-squares regression analysis show that relationships between measured values of specific conductance and chloride concentration have correlation coefficients ranging from 0.30 to 0.97. Analysis of streamflow for all major dissolved constituents is recommended with the purpose of attempting to describe the variations in the specific conductance/chloride concentration relationships.

Massachusetts↗
USGS2024

A history of cryohydrogeology modeling and recent advancements through the integration of solute transport

Groundwater flow systems and permafrost are interrelated because permafrost thaw enhances permeability, while groundwater flow can advect heat and accelerate permafrost thaw (McKenzie et al. 2021). Given amplified climate change in cold regions, there is renewed interest in ‘cryohydrogeology’, the study of groundwater in cold regions. Many data-driven studies have shown that permafrost thaw is leading to activated aquifers and increased baseflow across the pan-Arctic region (e.g. Walvoord and Striegl 2007, Evans et al. 2020). Empirical evidence of a subsurface ‘replumbing’ (Walvoord and Kurylyk 2016) in permafrost regions raises questions about the fate of sequestered contaminants in the North (Langer et al. 2023). We will discuss the history of and emerging opportunities in cryohydrogeological modeling, with a focus on recent contaminant transport modeling.

Conference Paper↗
USGS2026

Monazite and xenotime U-Pb geochronology and thermometry of the Blue Ridge and Inner Piedmont of North Carolina: Implications for the thermal-metamorphic evolution of the southern Appalachian metamorphic “core”

The southern Appalachian orogen preserves a complex distribution of metamorphism and deformation varying in timing, magnitude, and spatial extent. These complexities give rise to disparate interpretations for southern Appalachian tectonic evolution, which complicates the testing and interpretation of tectonic models in this system. New monazite (Mnz) and xenotime (Xtm) laser ablation split stream (LASS) analyses alongside Mnz-Xtm thermometry in the orogenic core in the eastern Blue Ridge (EBR), western Inner Piedmont (WIP), and Cat Square terranes (CST) of North Carolina yield new constraints that define distinct pro- and retrograde metamorphic events. The EBR preserves two prograde thermal events: the Taconic (∼470-440 Ma, >660°C) and Neoacadian (∼380-340 Ma, 600–700°C), separated by a period of cooling (exhumation?) and followed by garnet breakdown from 339 to 329 Ma. Evidence of pervasive Neoacadian ductile deformation in the EBR is largely limited to the Brevard fault zone (BFZ), indicating that a major rheological gradient existed across the BFZ during the Neoacadian and early Alleghanian. Southeast of the BFZ, in the WIP and CST, monazite data define a protracted Neoacadian evolution from early mineral growth at ∼405 Ma at ∼450–600°C to >700°C at ∼360 Ma, followed by early Alleghanian retrograde metamorphism and deformation (<345 Ma, 350–500°C). These constraints, together with previously reported thermobarometric data, define a P-T-t evolution for the WIP and CST consistent with Neoacadian crustal flow, while the coeval presence of a thermal-rheological boundary along the BFZ further supports a model of Neoacadian crustal “escape” flow within the orogen.

North Carolina↗
USGS2026

Origin of the Pd/Pt ratio of the J-M Reef, Stillwater Complex, Montana, USA

The J-M reef of the Stillwater Complex is characterized by a high Pd/Pt ratio (mean ~3.8 with a standard error of 0.03) with a homogeneous geospatial distribution at the deposit scale. In this contribution, we demonstrate that the Pd/Pt ratio of the reef is the product of equilibration of an immiscible sulfide liquid with a silicate melt rich in Pd relative to Pt. Despite the high tenors of the J-M reef sulfides (avg 2,700 ppm Pt and 770 ppm Pt), numerical modeling shows that the parental melts did not have extraordinary Pd and Pt concentrations. Instead, the initial composition of a plausible parental silicate melt can have Pd and Pt contents well within the expected range of a normal, mantle-derived partial melt (i.e., ~10–20 ppb for both Pd and Pt with Pd/Pt of ~1). The relative differences in the partitioning behavior of Pt and Pd between sulfide liquid and silicate melt are unlikely to produce a consistent Pd/Pt ratio across a wide range of silicate melt to sulfide liquid mass ratios (i.e., R factors). Instead, the pre-emplacement fractionation of Pt alloy from S-undersaturated silicate magma accounts for the homogeneous and high Pd/Pt ratio of the J-M reef. We show that batch equilibration of sulfide liquid with silicate melt can produce the high Pd/Pt ratios of the reef if the partition coefficients between sulfide liquid and silicate melt for Pd and Pt are extremely high (>10 6 ). In an alternative model, Pd enrichment could be achieved by sulfide upgrading in resident footwall mush even if the partition coefficients between sulfide liquid and silicate melt are relatively small (between 10 4 and 10 6 ) because the instantaneous mass ratio of silicate melt to sulfide liquid is small (R ≈ 100–700), so the partitioning behavior of Pt and Pd has little impact on the composition of sulfide liquid.

Montana↗
USGS1997

Analysis of minimum 7-day discharges and estimation of minimum 7-day, 2-year discharges for streamflow-gaging stations in the Brazos River basin, Texas

The minimum 7-day, 2-year discharge (7Q2) was estimated for each of 97 streamflow-gaging stations in the Brazos River Basin, Texas, with at least 10 years of unregulated or 10 years of regulated discharge data using the Pearson Type III distribution fitted by L-moment statistics of the annual minimum 7-day discharges. Forty-six stations have at least 10 years of unregulated discharge data only, 26 stations have at least 10 years of regulated discharge data only, and 25 stations have at least 10 years of unregulated and 10 years of regulated discharge data. Statistical tests were applied to the annual minimum 7-day discharges to determine if the unregulated and regulated data have trends; and to determine if the data before regulation are significantly different from the data after regulation. Results of the Mann-Kendall test indicate a significant trend at the 95-percent confidence level for 8 of the 46 unregulated-only stations, for 6 of the 26 regulated-only stations, and for 5 stations before regulation and for 10 stations after regulation of the 25 stations with both unregulated and regulated data. Results of the Wilcoxon rank-sum test indicate a significant difference between the unregulated and regulated annual minimum 7-day discharges at the 95-percent confidence level for 16 of the 25 stations with both types of data. The 7Q2 is zero for 31 of the 46 unregulated-only stations and for 9 of the 26 regulated-only stations. The 7Q2 also is zero for 9 stations before regulation and for 3 stations after regulation of the 25 stations with both unregulated and regulated data. The 7Q2 ranges from 33 to 631 cubic feet per second for the eight regulated-only stations on the mainstem Brazos River. For the seven stations on the mainstem Brazos River with at least 10 years of unregulated and 10 years of regulated discharge data, the 7Q2 ranges from 0 to 568 cubic feet per second before regulation and from 0.30 to 670 cubic feet per second after regulation. The 7Q2 increased during regulation for 19 of the 25 stations with both unregulated and regulated data. The effect of regulation for most stations generally was an increase in the magnitude of the 7Q2.

Texas↗
USGS2025

Geology and geochemistry of Ni-Co laterite occurrences of northern California and southern Oregon

Ni-Co laterite occurrences in the Klamath Mountains of southern Oregon and northern California contain Ni, Co, and Sc values comparable to global deposits. However, they are thin and limited in extent, often occurring as landslides and slumps. Olivine in the parent material contains Ni and Co and enstatite contains Sc. Through pervasive weathering, these elements where concentrated in Fe- and Mn-oxides. Unlike the mined Nickel Mountian deposit near Riddle, Oregon, these occurrences have no hydrous-Mg silicate minerals. Although the region experienced pervasive weathering in the Eocene, preservation of the laterite profiles was limited in the Klamath Mountains due to accelerated uplift and erosion compared to the Coast Range Provence.

Conference Paper↗
USGS2025

Confocal laser-scanning microscopy (CLSM)-based thermal maturity of Tasmanites and progress in standardization of fluorescence microspectrometry

Evaluation of thermal maturity in vitrinite-free or vitrinite-deficient sediments via fluorescence microspectrometry can provide relevant information related to petroleum exploration and thermal history assessment. However, variation in spectral fluorescence properties of alginite macerals with increasing thermal maturity is largely underexplored. Here, authors of this study have applied confocal laser-scanning microscopy (CLSM) in conjunction with fluorescence microspectrometry to a maturity series of marine Upper Devonian Tasmanites algae from the Ohio Shale (Huron Member) and a single sample from the Marcellus Formation of the Appalachian Basin. Spectral fluorescence properties of Tasmanites were evaluated in relation to orientation, measurement location, and the number of measurements per sample, and were compared to published literature. Emission spectra of Tasmanites from continuous wave laser excitation (405 nm) were acquired from sections perpendicular and parallel to bedding and at different positions within individual Tasmanites bodies. The results showed a progressive red-shift in emission maxima (λ max ) in a large sample sized maturity series ( N = 19), e.g., 493 to 578 nm for the perpendicular section at middle position. Further, blue-shifted apex and mineral-adjacent positions within sections perpendicular to bedding were observed, with the latter being reported here for the first time. While blue-shift at apex positions can be attributed to mechanical deformation-induced reorientation of photoselected fluorophores, the blue-shifted mineral-adjacent positions could result from strain loading and development of a plastic deformation region at the mineral contact zone with Tasmanites . A decrease in standard deviation with increasing number of measured emission maxima is well-observed, and 15 to 20 individual measurements per sample appears sufficient for low standard deviation and coefficient of variance. CLSM-derived thermal maturity parameters indicated that a moderate positive correlation of red/green quotient (Q 650/500 ; R 2 = 0.67) with solid bitumen reflectance (BR o in %) exists. For reproducible results, the determination of λ max and Q 650/500 should be conducted exclusively in the middle position at perpendicular and parallel sections of the polished whole-rock pellets, where the lowest standard deviation in measurement was observed. These results strengthen the suitability and relevance of the CLSM technique in thermal maturity studies of dispersed organic matter (DOM) and contribute to the standardization of fluorescence microspectrometry methods in organic petrology investigation.

Kentucky, Ohio, Virginia, West Virginia↗
USGS2026

The mineral chemistry networks of tin and tungsten reflect metallogenic eras of the Mesozoic

Continental remobilization is a crucial driver of metallogenesis and the formation of ore deposits. Some of the world’s largest mineral deposits of the economically valuable elements tin (Sn), tungsten (W), gold (Au), copper (Cu), lead (Pb), and zinc (Zn) formed during the Mesozoic Era. Additionally, the chemistry and distribution of the elements Sn and W have been investigated in previous studies to understand planetary formation and differentiation processes. These two elements are largely co-located during certain South China Mesozoic metallogenic events but are not co-located during other time periods in the same regions. Here, we investigated the mineral chemistry network similarities and dissimilarities of Sn and W to understand their mineral formation and distribution during the Mesozoic Era and throughout Earth history. Mineral chemistry network community detection analysis and electronegativity associations among mineral constituent elements of Sn minerals and W minerals indicate that the elements have similar chemistry among their oxide minerals. However, Sn forms a much wider range of minerals that also contain S compared to W, which occurs in a limited number of S-containing minerals. The divergent constituent element interactions among S-containing Sn minerals and W minerals reflect the redox sensitivity and importance of oxygen (O) fugacity in Sn mineral formation. Conversely, extensive W mineral deposits are known to form at both high and low O fugacities. The similarities and differences between the mineral chemistry networks of Sn and W reflect the mineral distribution of the two elements in the Sn-W mineralization event from 160 to 139 Ma vs. the Sn–uranium (U) mineralization event from 125 to 98 million years ago (Ma). The mineral chemistry and distribution of Mesozoic Sn and W deposits illustrate the contrasting importance of redox and O fugacity on the mineral formation of different elements, and the dynamic crustal evolution that took place during this period of Earth history.

Geosciences↗
USGS2025

Melt generation sources and conditions in the wake of a migrating slab window: Geochemistry and petrology of the million-year history of primitive volcanism at Clear Lake volcanic field, California

Clear Lake volcanic field (CLVF) is the northernmost and youngest (~2.2 Ma to 8 ka) of the volcanic centers distributed along the San Andreas transform fault in western California. The initial phase of CLVF volcanism (interval one) occurred between ~2.2 and 1.3 Ma and extends ~35 km southeast of Clear Lake, forming a semi-continuous upland plateau capped by lava flows, with isolated volcanic remnants on the periphery. This volcanism is broadly characterized by geochemically primitive compositions that reflect three source compositions and conditions of melt generation. (1) Partial melting of upwelling asthenospheric mantle lherzolite at moderate pressures (1.2–1.4 GPa) and temperatures (1297–1329 °C) produced high-CaO (9.8–11.3 wt %) basalts with high Al 2 O 3 (16.8–17.6 wt %), Mg#s (66–70), MgO (8–10 wt %), Ni (103–262 μg/g), and Cr (284–609 μg/g). These high-CaO basalts contain olivine (Fo 87–91 ) phenocrysts with Cr-spinel inclusions ± subordinate plagioclase and crop out only in the southern part of the CLVF. (2) Partial melting of depleted sub-continental lithospheric mantle harzburgite at variable pressures (0.7–1.5 GPa) and temperatures (1097–1299 °C) produced a compositional continuum of med-K 2 O, calc-alkaline, high-MgO basalts through high-MgO andesites with high Mg#s (67–77), MgO (8–14 wt %) and high Ni and Cr abundances (154–439 and 340–1124 μg/g, respectively). Mineral assemblages are olivine (Fo 88–93 ) with Cr-spinel inclusions ± subordinate clinopyroxene, orthopyroxene and plagioclase. Small (<2.5 cm) mantle harzburgite xenoliths and mantle olivine xenocrysts are also found in several of these samples. These high-MgO basalts through andesites represent the largest volume of primitive compositions and have erupted predominantly along the main, fault-controlled northwest-southeast trending axis of volcanism with peripheral outcrops to the north, west, and east. (3) Partial melting of the Gorda eclogite slab edge produced adakitic silicic slab melts with strong depletion in the heavy rare earth elements (Yb = 0.6 μg/g). Subsequent reaction of those melts with depleted ultramafic rocks during ascent imprinted the adakitic dacites with high Mg#s (65–78) and elevated Ni (117–210 μg/g) and Cr (191–283 μg/g). Phenocrysts of orthopyroxene (En 87–94 ) with spinel inclusions (Cr# = 80–88) and extremely Ni-rich (9483 μg/g) olivine cores (Fo 84–93 ) record those reactions. Small-volume outcrops of the adakites on the eastern periphery of the CLVF track the passing slab edge. The trio of melting sources recorded by early CLVF magmatism reflect the tectonically complex environment and the hot (1097–1329 °C), shallow (0.7–1.5 GPa) melting conditions for these primitive compositions and provide estimates of the heat delivered to the crust. Over time, this flux led to maturation of the CLVF magmatic system toward the more voluminous and silicic volcanism that characterizes the balance of its subsequent volcanic history and maintains the present-day anomalously high heat flow in the region. The current interval (interval four) of volcanic activity at CLVF is characterized by low-volume, fault-controlled eruptions of basaltic andesite and andesite suggestive of mantle magma and heat delivery to the crust, similar to interval one. This analogous activity provides motivation for the current study and begs the question of whether the system is undergoing thermal priming for renewed silicic volcanism.

California↗
USGS2025

Origin of the high Pd/Pt ratio of the J-M Reef, Stillwater Complex Montana USA

The J-M Reef of the Stillwater Complex exhibits a high and consistent Pd/Pt ratio (~3.8). This ratio results from the equilibration of an immiscible sulfide liquid with a relatively high Pd/Pt silicate melt rather than an unusually Pd- and Pt-enriched parental melt. Numerical modeling suggests that the original silicate melt contained typical mantle-derived concentrations of Pd and Pt (~10–20 ppb Pd/Pt ~1). The partitioning of Pt and Pd between sulfide liquid and silicate melt alone cannot explain the consistently high Pd/Pt ratio across variable melt-to-sulfide mass ratios (R factors). Instead Pt-depletion caused by the early fractionation of Pt-alloy from S-undersaturated silicate magma likely established the high Pd/Pt signature. High Pd/Pt ratios can form through batch equilibration of sulfide liquid with silicate melt if partition coefficients are extremely high (>10⁶). Alternatively Pd enrichment may result from sulfide upgrading within the resident footwall mush under smaller partition coefficients (10⁴–10⁶) in this model the instantaneous R factors remain low (R ≈ 100–700). This limits the impact of Pt and Pd partitioning on sulfide composition and helps explain the Pd-enriched character of the J-M Reef.

Montana↗
USGS1977

Acid-rain weathering of a metasedimentary rock basin, Herkimer County, New York

A geochemical balance of major chemical constituents of precipitation inflow with those of surface-water outflow was used to evaluate the effect of acid rainfall (average pH = 4.3) on weathering rates of metasedimentary rocks underlying a surface-water basin in New York State. Precipitation samples and surface-water samples show that approximately 45 percent of the net cation outflow is due to weathering by precipitation acidity. The remaining 55 percent of the cation load in the outflow is attributed to interactions between atmosphere, rock, and soil water in the unsaturated zone. Comparison of the acidity of acid precipitation and air-equilibrated distilled water suggests that since preindustrial time, precipitation acidity has probably increased weathering rates for this basin approximately 75 percent. The increased acidity of the precipitation may also increase the rate of dissolution of heavy metals from water-piping systems.

New York↗
USGS1997

Water-quality assessment of south-central Texas: Occurrence and distribution of volatile organic compounds in surface water and ground water, 1983-94, and implications for future monitoring

The study area of the South-Central Texas study unit of the National Water-Quality Assessment Program comprises the Edwards aquifer in the San Antonio region and its catchment area. The first phase of the assessment includes evaluation of existing water-quality data for surface water and ground water, including volatile organic compounds, to determine the scope of planned monitoring. Most analyses of volatile organic compounds in surface water are from the National Pollutant Discharge Elimination System sites in San Antonio, Texas. Nine volatile organic compounds were detected at the six sites. The three compounds with the most detections at National Pollutant Discharge Elimination System sites are 1,2,4-trimethylbenzene, toluene, and xylene. Analysis of volatile organic compounds in ground water was limited to Edwards aquifer wells. Twenty-eight volatile organic compounds were detected in samples from 89 wells. The five most commonly detected compounds in samples from wells, in descending order, are tetrachloroethene, trichloroethene, bromoform, chloroform, and dibromochloromethane. Detections of volatile organic compounds in surface water and ground water within the South-Central Texas study area are limited to site-specific sources associated with development; therefore, planned monitoring for possible detections of volatile organic compounds as part of the National Water-Quality Assessment Program will emphasize areas of expanding population and development. Monitoring of volatile organic compounds is planned at National Pollutant Discharge Elimination System sites, at basic fixed surface-water sites, and in the ground-water study-unit surveys.

Texas↗