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USGS2025

Terrebonne Basin, Gulf of Mexico gas hydrate resource evaluation and 3-D modeling of basin-scale sedimentation, salt tectonics, and hydrate system evolution since the early Miocene

In assessing methane hydrate as a potential transitional energy source, quantification of in-place volumes of gas is a first step—and yet, global, regional, and even local estimates of gas volumes contained within hydrate are highly variable, including within the extensively-studied Gulf of Mexico (GoM) gas hydrate province. Here, we construct the first 3-D basin and hydrocarbon system model of the Terrebonne Basin (Walker Ridge protraction area, northern GoM) to estimate in-place resources contained as gas within hydrate, as well as to provide the first estimate of in-place resources contained within free gas accumulations in the basin. The resultant model-predicted 3-D distributions (and saturations) of hydrate are consistent with independent seismic interpretation and borehole observations. This study reveals both sedimentation-driven and salt diapir-driven gas hydrate recycling produce elevated hydrate saturations in the basin (“recycling” occurs when relative upward shifts of the gas hydrate stability zone (GHSZ) cause hydrate dissociation, generating buoyant free gas that may reaccumulate as higher-saturation hydrate at the new base of GHSZ). An important finding of this study (particularly given that, globally, the source of methane in marine hydrate systems tends to be poorly understood) is that microbial sources can explain most or all hydrate occurrences in Terrebonne Basin. We calculate that ∼32 × 10 9 m 3 (∼1.1 10 12 ft 3 ) of methane gas is trapped within hydrate accumulations throughout Terrebonne Basin, while nearly 2 × 10 9 m 3 (∼67 × 10 9 ft 3 ) of methane occurs as free gas at high saturations within sandy reservoirs beneath the GHSZ and ∼35 × 10 9 m 3 (∼1.2 × 10 12 ft 3 ) occurs as free gas at low saturations within muddy units beneath the GHSZ. In total, our calibrated 3-D model predicts that nearly 70 × 10 9 m 3 (∼2.5 × 10 12 ft 3 ) of microbial methane is trapped as gas hydrate and free gas in the Terrebonne Basin.

Marine and Petroleum Geology↗

USGS1961

Sandstone-type uranium deposits at Ambrosia Lake, New Mexico-An interim report

The Ambrosia Lake district in northwestern New Mexico is the most important uranium mining and milling district in the United States. Together with the nearby Laguna district it contains more than 50 percent of the nation's reserves.Most of the ore occurs in the Morrison formation of Late Jurassic age as elongate, tabular, mantolike bodies principally in the upper half of the Westwater Canyon sandstone member and near the base of the Poison Canyon sandstone tongue (9). Individual deposits are distributed along two easterly trending belts 2 to 3 miles apart. The ore bodies are as much as 3,000 feet long, several hundred feet wide, and 100 feet thick. Depths to the ore range from 0 to 2,200 feet. Some ore is also mined from the Todilto limestone of Late Jurassic age and from the Dakota sandstone of Early (?) and Late Cretaceous age.Two types of unoxidized ore are recognized: prefault ore, which is considered to be primary, and postfault ore, which may be redistributed. The prefault ore shows no obvious relationship to tectonic structures but appears to be controlled by a variety of sedimentary structures. Postfault ore is controlled by a combination of sedimentary and tectonic structures. Disseminated carbonaceous matter, believed to be plant derived, appears to be the dominant control in the localization of the uranium .The ore mineralogy is comparatively simple, and coffinite is by far the most abundant ore mineral. Molybdenum, selenium, vanadium, and iron occur in anomalous quantities in the deposits in both oxidized and unoxidized minerals.U/eU ratios and radioisotope distribution indicate almost universal disequilibrium and fairly recent migration of radioisotopes in all deposits that have been sampled.Further studies on the organic carbonaceous matter, sandstone alteration, age determinations, and sulfur isotope composition are required to obtain a better understanding of the source, transportation, and deposition of uranium and other elements in the deposits .

New Mexico↗

USGS2011

Reserve growth in oil pools of Alberta: Model and forecast

Reserve growth is recognized as a major component of additions to reserves in most oil provinces around the world, particularly in mature provinces. It takes place as a result of the discovery of new pools/reservoirs and extensions of known pools within existing fields, improved knowledge of reservoirs over time leading to a change in estimates of original oil-in-place, and improvement in recovery factor through the application of new technology, such as enhanced oil recovery methods, horizontal/multilateral drilling, and 4D seismic. A reserve growth study was conducted on oil pools in Alberta, Canada, with the following objectives: 1) evaluate historical oil reserve data in order to assess the potential for future reserve growth; 2) develop reserve growth models/ functions to help forecast hydrocarbon volumes; 3) study reserve growth sensitivity to various parameters (for example, pool size, porosity, and oil gravity); and 4) compare reserve growth in oil pools and fields in Alberta with those from other large petroleum provinces around the world. The reported known recoverable oil exclusive of Athabasca oil sands in Alberta increased from 4.5 billion barrels of oil (BBO) in 1960 to 17 BBO in 2005. Some of the pools that were included in the existing database were excluded from the present study for lack of adequate data. Therefore, the known recoverable oil increased from 4.2 to 13.9 BBO over the period from 1960 through 2005, with new discoveries contributing 3.7 BBO and reserve growth adding 6 BBO. This reserve growth took place mostly in pools with more than 125,000 barrels of known recoverable oil. Pools with light oil accounted for most of the total known oil volume, therefore reflecting the overall pool growth. Smaller pools, in contrast, shrank in their total recoverable volumes over the years. Pools with heavy oil (gravity less than 20o API) make up only a small share (3.8 percent) of the total recoverable oil; they showed a 23-fold growth compared to about 3.5-fold growth in pools with medium oil and 2.2-fold growth in pools with light oil over a fifty-year period. The analysis indicates that pools with high porosity reservoirs (greater than 30 percent porosity) grew more than pools with lower porosity reservoirs which could possibly be attributed to permeability differences between the two types. Reserve growth models for Alberta, Canada, show the growth at field level is almost twice as much as at pool level, possibly because the analysis has evaluated fields with two or more pools with different discovery years. Based on the models, the growth in oil volumes in Alberta pools over the next five-year period (2006-2010) is expected to be about 454 million barrels of oil. Over a twenty-five year period, the cumulative reserve growth in Alberta oil pools has been only 2-fold compared to a 4- to- 5-fold increase in other petroleum producing areas such as Saskatchewan, Volga-Ural, U.S. onshore fields, and U.S. Gulf of Mexico. However, the growth at the field level compares well with that of U.S. onshore fields. In other petroleum provinces, the reserves are reported at field levels rather than at pool levels, the latter basically being the equivalent of individual reservoirs. ?? 2010 by the Canadian Society of Petroleum Geologists.

Bulletin of Canadian Petroleum Geology↗

USGS2004

Isotopic, geochemical, and temporal characterization of Proterozoic basement rocks in the Quitovac region, northwestern Sonora, Mexico: Implications for the reconstruction of the southwestern margin of Laurentia

A detailed geochemical characterization of 19 representative Proterozoic basement rocks in the Quitovac region in northwestern Sonora, Mexico, has identified two distinct Paleoproterozoic basement blocks that coincide spatially with the previously proposed Caborca and "North America" blocks. New U-Pb zircon geochronology revises their age ranges, the Caborca (1.78-1.69 Ga) and "North America" (1.71-1.66 Ga) blocks at Quitovac, and precludes a simple age differentiation between them. In addition, Grenvillian-age granitoids (ca. 1.1 Ga), spatially associated with the Caborca block have been identified at Quitovac. Nd isotopes and major- and trace-element geochemistry support the distinction of these Paleoproterozoic blocks. Granitoids of the "North America" block are characterized by depleted εNd values (3.4-3.9) and younger Nd model ages (1800-1740 Ma) and have lower K2O, Y, Rb, Ba, Th, REE, and Fe/Mg values than coeval rocks of the Caborca block. The Caborca block granitoids are likewise characterized by slightly less depleted εNd (0.6-2.6) and older Nd model ages (2070-1880 Ma). Despite the subtle differences, granitoids from both the Caborca and "North America" blocks exhibit island arc-like affinities. We propose that the Proterozoic basement rocks from the Quitovac region are an extension of the Proterozoic crustal provinces in the southwestern United States. Specifically, rocks of the Caborca block exhibit an affinity to rocks of either the Yavapai province or the Mojave-Yavapai transition zone, whereas rocks of the "North America" block have signatures similar to those of the Mazatzal province or possibly the Yavapai province of Arizona. The new isotopic ages and geochemical data do not support the existence of the Late Jurassic Mojave-Sonora megashear at Quitovac, as originally proposed. However, the Quitovac region accounts only for a small fraction of the Proterozoic basement in Sonora, so these findings do not eliminate the possibility of a megashear elsewhere in northern Sonora. Our new data create the possibility of alternative hypotheses for the distribution of Paleoproterozoic crustal provinces in southwestern North America that affect reconstructions of the original southwestern margin of Laurentia, and reduce uncertainties in the configuration, timing, and existence of the Proterozoic supercontinent, Rodinia.

Quitovac↗

USGS2012

Ecosystem services valuation to support decisionmaking on public lands—A case study of the San Pedro River watershed, Arizona

This report details the findings of the Bureau of Land Management–U.S. Geological Survey Ecosystem Services Valuation Pilot Study. This project evaluated alternative methods and tools that quantify and value ecosystem services, and it assessed the tools’ readiness for use in the Bureau of Land Management decisionmaking process. We tested these tools on the San Pedro River watershed in northern Sonora, Mexico, and southeast Arizona. The study area includes the San Pedro Riparian National Conservation Area (managed by the Bureau of Land Management), which has been a focal point for conservation activities and scientific research in recent decades. We applied past site-specific primary valuation studies, value transfer, the Wildlife Habitat Benefits Estimation Toolkit, and the Integrated Valuation of Ecosystem Services and Tradeoffs (InVEST) and Artificial Intelligence for Ecosystem Services (ARIES) models to value locally important ecosystem services for the San Pedro River watershed—water, carbon, biodiversity, and cultural values. We tested these approaches on a series of scenarios to evaluate ecosystem service changes and the ability of the tools to accommodate scenarios. A suite of additional tools were either at too early a stage of development to run, were proprietary, or were place-specific tools inappropriate for application to the San Pedro River watershed. We described the strengths and weaknesses of these additional ecosystem service tools against a series of evaluative criteria related to their usefulness for Bureau of Land Management decisionmaking. Using these tools, we quantified gains or losses of ecosystem services under three categories of scenarios: urban growth, mesquite management, and water augmentation. These results quantify tradeoffs and could be useful for decisionmaking within Bureau of Land Management district or field offices. Results are accompanied by a relatively high level of uncertainty associated with model outputs, valuation methods, and discount rates applied. Further guidance on representing uncertainty and applying uncertain results in decisionmaking would benefit both tool developers and those offices in using ecosystem services to compare management tradeoffs. Decisionmakers and Bureau of Land Management managers at the State-, district-, and field-office level would also benefit from continuing model improvements, training, and guidance on tool use that can be provided by the U.S. Geological Survey, the Bureau of Land Management, and the Department of the Interior. Tradeoffs were identified in the level of effort needed to parameterize and run tools and the amount and quality of information they provide to the decision process. We found the Wildlife Habitat Benefits Estimation Toolkit, Ecosystem Services Review, and United Nations Environment Programme–World Conservation Monitoring Centre Ecosystem Services Toolkit to be immediately feasible for application by the Bureau of Land Management, given proper guidance on their use. It is also feasible for the Bureau of Land Management to use the InVEST model, but in early 2012 the process of parameterizing the model required resources and expertise that are unlikely to be available in most Bureau of Land Management district or field offices. Application of past primary valuation is feasible, but developing new primary-valuation studies is too time consuming for regular application. Value transfer approaches (aside from the Wildlife Habitat Benefits Estimation Toolkit) are best applied carefully on the basis of guidelines described in this report, to reduce transfer error. The ARIES model can provide useful information in regions modeled in the past (Arizona, California, Colorado, and Washington), but it lacks some features that will improve its usability, such as a generalized model that could be applied anywhere in the United States. Eleven other tools described in this report could become useful as the tools more fully develop, in high-profile cases for which additional resources are available for tool application or in case-study regions where place-specific models have already been developed. To improve the value of these tools in decisionmaking, we suggest scientific needs that agencies such as U.S. Geological Survey can help meet—for instance, development and support of data archives. Such archives could greatly reduce resource needs and improve the reliability and consistency of results. Given the rapid state of evolution in the field, periodic follow-up studies on ecosystem services tools would help to ensure that the Bureau of Land Management and other public land management agencies are kept up to date on new tools and features that bring ecosystem services closer to readiness for use in regular decisionmaking.

Arizona;Sonora↗

USGS1944

"Ribbon rock", an unusual beryllium-bearing tactite

The beryllium deposits at Iron Mountain, near the northern end of the Sierra Cuchillo in Sierra and Socorro Counties, New Mexico, are unusual products of contact metamorphism. They occur in irregular bodies of tactile formed by replacement of Paleozoic limestone, generally at or near contacts with small intrusive masses of rhyolite, aplite, and fine-grained granite. The metamorphism took place in mid-Tertiary time. Beryllium is present chiefly in the complex silicate minerals helvite and danalite, and is a minor constituent of the garnet grossularite, a boron-bearing idocrase, and chlorite. These minerals are known to occur in noteworthy concentrations in only one type of rock, a peculiar rhythmically layered variety of tactile to which the name "ribbon rock" is given. The structure of such tactite is very conspicuous, and appears in section as thin, finely crenulated bands of magnetite alternating with similar bands of silicate minerals and finely crystalline fluorite. Concentric banding about fluorite-rich pod-like masses is common. Bodies of "ribbon rock" range in size from inch-thick lenses to large masses amounting to thousands of tons; most appear to have been formed along contacts between re-crystallized limestone and massive magnetite-andradite tactite, chiefly by replacing fluids penetrating the limestone from fractures. The layered structure is interpreted as a diffusion effect.The formation of massive and "ribbon rock" tactites can be traced through a range of falling temperature from a stage characterized by deposition from iron-rich vapors to a stage in which hydrothermal solutions were dominant. Both vapors and liquids appear to have been acid. Reducing conditions undoubtedly existed during the latter part of the hydrothermal stage. The occurrence of beryllium in "ribbon rock," but not in typical massive tactite, may signify that its compounds in deposits at or near intrusive contacts are confined to rocks of hydrothermal origin. The occurrence of "ribbon rock" is suggested as a potentially useful clue for recognition of beryllium-bearing contact deposits elsewhere; at least two other occurrences of what apparently is "ribbon rock" have been described in the literature.

New Mexico↗

USGS2016

Geochemistry of formation waters from the Wolfcamp and “Cline” shales: Insights into brine origin, reservoir connectivity, and fluid flow in the Permian Basin, USA

Despite being one of the most important oil producing provinces in the United States, information on basinal hydrogeology and fluid flow in the Permian Basin of Texas and New Mexico is lacking. The source and geochemistry of brines from the basin were investigated (Ordovician- to Guadalupian-age reservoirs) by combining previously published data from conventional reservoirs with geochemical results for 39 new produced water samples, with a focus on those from shales. Salinity of the Ca–Cl-type brines in the basin generally increases with depth reaching a maximum in Devonian (median = 154 g/L) reservoirs, followed by decreases in salinity in the Silurian (median = 77 g/L) and Ordovician (median = 70 g/L) reservoirs. Isotopic data for B, O, H, and Sr and ion chemistry indicate three major types of water. Lower salinity fluids (<70 g/L) of meteoric origin in the middle and upper Permian hydrocarbon reservoirs (1.2–2.5 km depth; Guadalupian and Leonardian age) likely represent meteoric waters that infiltrated through and dissolved halite and anhydrite in the overlying evaporite layer. Saline (>100 g/L), isotopically heavy (O and H) water in Leonardian [Permian] to Pennsylvanian reservoirs (2–3.2 km depth) is evaporated, Late Permian seawater. Water from the Permian Wolfcamp and Pennsylvanian “Cline” shales, which are isotopically similar but lower in salinity and enriched in alkalis, appear to have developed their composition due to post-illitization diffusion into the shales. Samples from the “Cline” shale are further enriched with NH 4 , Br, I and isotopically light B, sourced from the breakdown of marine kerogen in the unit. Lower salinity waters (<100 g/L) in Devonian and deeper reservoirs (>3 km depth), which plot near the modern local meteoric water line, are distinct from the water in overlying reservoirs. We propose that these deep meteoric waters are part of a newly identified hydrogeologic unit: the Deep Basin Meteoric Aquifer System. Chemical, isotopic, and pressure data suggest that despite over-pressuring in the Wolfcamp shale, there is little potential for vertical fluid migration to the surface environment via natural conduits.

New Mexico, Texas↗

USGS2023

Genesis of the Questa Mo porphyry deposit and nearby polymetallic mineralization, New Mexico, USA

The Oligocene Latir magmatic center in northern New Mexico is an exceptionally well-exposed volcanoplutonic complex that hosts a variety of magmatic-hydrothermal deposits, ranging from relatively deep, F-rich porphyry Mo mineralization to shallower epithermal deposits. We present new whole-rock chemical and isotopic data for plutonic rocks from the Latir magmatic center, including extensive sampling of drill core samples of intrusive rocks from the Questa porphyry Mo deposit. These data document temporal chemical trends of porphyry-related mineralization that occurred after caldera-forming magmatism and during postcaldera batholith assembly. Silicic magmas were generated multiple times throughout the history of the Latir magmatic center, but few are associated with the formation of a mineral deposit. Whole-rock trace element ratios and Sr, Nd, and Pb isotope compositions vary throughout the protracted history of silicic magmatism. The caldera-forming ignimbrite and early phase of postcaldera intrusions are unmineralized, more enriched in high field strength elements, and generally contain less radiogenic Sr and Pb and more radiogenic Nd than later intrusions. The Questa porphyry Mo deposit formed immediately after the most isotopically primitive phase of the batholith was assembled, ruling out simple reworking of juvenile mantle-derived crust as the source for mineralizing magmas. Rhyolite dikes associated with polymetallic sulfide deposits intruded ~800 k.y. after Mo mineralization, and Nd isotope data indicate that these dikes are associated with different batches of magma and are unrelated to the Mo-mineralizing intrusions at the Questa mine. Together, these data indicate that the source of magmas changed significantly throughout the 10-m.y. history of the magmatic center. We assess multiple genetic models for porphyry-related magmatism against this data set, favoring models with discrete periods of magma genesis from a deep hybridized zone in the lower crust giving rise to the punctuated periods of mineralization. These observations suggest that the formation of mineral deposits within a central magmatic locus is likely the result of the piecemeal assembly of individual hydrothermal-magmatic systems, and that distal and younger polymetallic mineralization commonly observed near known porphyry deposits represents decoupled processes.

New Mexico↗

USGS1999

Evolution of Cupido and Coahuila carbonate platforms, early Cretaceous, northeastern Mexico

The Cupido and Coahuila platforms of northeastern Mexico are part of the extensive carbonate platform system that rimmed the ancestral Gulf of Mexico during Barremian to Albian time. Exposures of Cupido and Coahuila lithofacies in several mountain ranges spanning an ∼80000 km 2 area reveal information about platform morphology and composition, paleoenvironmental relations, and the chronology of platform evolution. New biostratigraphic data, integrated with carbon and strontium isotope stratigraphy, significantly improve chronostratigraphic relations across the region. These data substantially change previous age assignments of several formations and force a revision of the longstanding stratigraphy in the region. The revised stratigraphy and enhanced time control, combined with regional facies associations, allow the construction of cross sections, isopach maps, and time-slice paleogeographic maps that collectively document platform morphology and evolution. The orientation of the Cupido (Barremian-Aptian) shelf margin was controlled by the emergent Coahuila basement block to the northwest. The south-facing margin is a high-energy grainstone shoal, whereas the margin facing the ancestral Gulf of Mexico to the east is a discontinuous rudist-coral reef. A broad shelf lagoon developed in the lee of the Cupido margin, where as much as 660 m of cyclic peritidal deposits accumulated. During middle to late Aptian time, a major phase of flooding forced a retrograde backstep of the Cupido platform, shifting the locus of shallow-marine sedimentation northwestward toward the Coahuila block. This diachronous flooding event records both the demise of the Cupido shelf and the consequent initiation of the Coahuila ramp. The backstepped Coahuila ramp (Aptian-Albian) consisted of a shallow shoal margin separating an interior evaporitic lagoon from a low-energy, muddy deep ramp. More than 500 m of cyclic carbonates and evaporites accumulated in the evaporitic lagoon during early to middle Albian time. Restriction of the platform interior dissipated by middle to late Albian time with the deposition of peloidal, miliolid-rich packstones and grainstones of the Aurora Formation. The Coahuila platform was drowned during latest Albian to early Cenomanian time, and the deep-water laminites of the Cuesta del Cura Formation were deposited. This study fills in a substantial gap in the Cretaceous paleogeography of the eastern Gulf of Mexico coast, improving regional correlations with adjacent hydrocarbon-rich platforms. The enhanced temporal relations and chronology of events recorded in the Cupido and Coahuila platforms significantly improve global correlations with coeval, economically important platforms worldwide, perhaps contributing to the determination of global versus regional controls on carbonate platform evolution during middle Cretaceous time.

Geological Society of America Bulletin↗

USGS2018

Early arc development recorded in Permian–Triassic plutons of the northern Mojave Desert region, California, USA

Permian–Middle Triassic plutons in the northern Mojave Desert, USA, are emplaced into the cryptic El Paso terrane, which is characterized by a northwest-striking belt of deep marine eugeoclinal strata juxtaposed against Proterozoic basement and its miogeoclinal cover. Fourteen new zircon U-Pb ages from the El Paso Mountains and Lane Mountain region of the Mojave Desert record nearly continuous magmatism occurring between ca. 275 and 240 Ma. These ages, which are taken to record the onset of subduction-related magmatism along the southwestern Laurentian margin, are older than the earliest arc plutons documented in the southern Sierra Nevada region to the north and in the Transverse Ranges to the south. They overlap, however, with Permian arc plutons documented in Sonora, Mexico. Dated plutons are compositionally variable, but can be characterized as intermediate to felsic, calcic to calc-alkalic, and having chemistries consistent with generation in an arc setting. Whole rock Sr-Nd isotopic compositions vary widely from relatively primitive (Sr i = 0.7035, initial εNd = +3, initial εHf in zircon = +13) to moderately evolved (Sr i = 0.708, initial εNd = –5, initial εHf in zircon = –3). Isotopic signatures differ considerably from partially coeval Triassic suites of the Transverse Ranges and central Mojave, which are more evolved and consistent with emplacement in Proterozoic continental crust of the Mojave province. They also differ considerably from those typical of intermediate plutons generated in intra-oceanic arcs, which are overall much more mantle-like. This suggests that the underpinnings of the El Paso terrane may be at least partly composed of continental crust and that magmas emplaced into the terrane may have been variably contaminated by crustal components. This is supported by the presence of Precambrian and early Paleozoic zircon inheritance recorded in some plutons. In all isotopic systems, values are the most evolved in the oldest plutons (ca. 275–270 Ma), becoming more juvenile in the Middle Triassic. These temporal trends, together with pluton fabrics and new estimates of Permian plate vectors, are interpreted to reflect generation of the earliest arc in a contractional setting that may have driven crustal thickening and a greater involvement of crustal materials in Permian magmas. This result supports a model of forced subduction initiation, which is favored by a change in plate motions along a previously weak margin, and predicts an initial compressive state in the upper plate. The uniformly primitive signatures of Triassic melts are taken to indicate a change to a transtensional upper-plate stress regime that promoted the development of more voluminous, primarily mantle-derived melts. Regional pluton age patterns suggest that arc magmatism initiated in restricted areas of the southwestern Laurentian margin (northern Mojave, Sonora) and then migrated north and south ultimately becoming a continuous arc by Jurassic time.

California↗

USGS2008

Davis Pond freshwater prediversion biomonitoring study: freshwater fisheries and eagles

In January 2001, the construction of the Davis Pond freshwater diversion structure was completed by the U.S. Army Corps of Engineers. The diversion of freshwater from the Mississippi River is intended to mitigate saltwater intrusion from the Gulf of Mexico and to lessen the concomitant loss of wetland areas. In addition to the freshwater inflow, Barataria Bay basin would receive nutrients, increased flows of sediments, and water-borne and sediment-bound compounds. The purpose of this biomonitoring study was, therefore, to serve as a baseline for prediversion concentrations of selected contaminants in bald eagle ( Haliaeetus leucocephalus ) nestlings (hereafter referred to as eaglets), representative freshwater fish, and bivalves. Samples were collected from January through June 2001. Two similarly designed postdiversion studies, as described in the biological monitoring program, are planned. Active bald eagle nests targeted for sampling eaglet blood (n = 6) were generally located southwest and south of the diversion structure. The designated sites for aquatic animal sampling were at Lake Salvador, at Lake Cataouatche, at Bayou Couba, and along the Mississippi River. Aquatic animals representative of eagle prey were collected. Fish were from three different trophic levels and have varying feeding strategies and life histories. These included herbivorous striped mullet ( Mugil cephalus ), omnivorous blue catfish ( Ictalurus furcatus ), and carnivorous largemouth bass ( Micropterus salmoides ). Three individuals per species were collected at each of the four sampling sites. Freshwater Atlantic rangia clams ( Rangia cuneata ) were collected at the downstream marsh sites, and zebra mussels ( Dreissena spp.) were collected on the Mississippi River. The U.S. Geological Survey (USGS) Biomonitoring of Environmental Status and Trends (BEST) protocols served as guides for fish sampling and health assessments. Fish are useful for monitoring aquatic ecosystems because they accumulate pesticides and other contaminants. Biomarker data on individual fish, generated at the USGS National Wetlands Research Center (Lafayette, La.), included percent white blood cells in whole blood, spleen weight to body weight ratio, liver weight to body weight ratio, condition factor, splenic macrophage aggregates, and liver microsomal 7-ethoxyresorufin-o-deethylase (EROD) activity. Fish age was estimated by comparing total lengths with values from the same species in the Southeast United States as determined from the literature. Contaminant analyses were coordinated by the U.S. Fish and Wildlife Service (USFWS) Analytical Control Facility (Laurel, Md.), where residues of organochlorine (OC) pesticides, total polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), aliphatic hydrocarbons (AHs), and trace elements were determined. The organic contaminant data were generated at the Mississippi State University Chemical Lab (Mississippi State, Miss.), and the inorganic contaminant data were generated by the Texas A&M University Geochemical and Environmental Research Group (College Station, Tex.). Statistical tests were performed to assess relationships among contaminants, fish age, fish species, and collection sites. Trends in interspecific differences among fish in concentrations of contaminants were noted. Striped mullet (hereafter mullet) frequently displayed the highest chemical concentrations. Levels of contaminants were generally higher in samples obtained from the Mississippi River than in those collected from the diversion area and were higher in mussels and clams (hereafter bivalves) than in fish. Because the Mississippi River sampling site for mullet and largemouth bass was downriver of the structure and south of New Orleans and the catfish site was upriver, the downriver data may not be directly reflective of the results from the receiving waters at the Davis Pond structure. Compared to the Caernarvon freshwater prediversion study in 1990 that assessed possible influx of contaminants with the freshwater diversion, contaminant levels in fishes and bivalves in this study were generally lower, yet three nontoxic inorganic elements in Davis Pond fish samples exhibited ranges of concentrations that were more than two times higher than did those from Caernarvon. Levels in bivalves were different between diversions but about equal in the numbers of trace elements showing high levels per location. Contaminant values were compared to those listed in various literature and agency sources, both regional and national, including the National Contaminant Biomonitoring Program (NCBP), in which the 85th percentile and above represents what is considered to be an elevated contaminant concentration and cause for concern. Generally, bivalves were at the high end of their ranges for both organic and inorganic contaminants. In this study, OCs were detectable in 67 percent of fish from the Mississippi River site, ranging from 0.15 to 1.09 μg/g wet weight (ww) or fresh weight (fw), and in 11 percent of the fish from the marsh sites, ranging from 0.06 to 0.612 μg/g ww. Bivalves from the Mississippi River had OC levels of 0.096 μg/g ww, whereas none were detectable in bivalves at the marsh sites. In this study, p,p ’-dichlorodiphenyldichloroethylene ( p,p’ -DDE) (a biodegradation product of DDT [dichlorodiphenyl trichloroethane]) and total PCBs were the most frequently detected OCs and were primarily from the Mississippi River. For total OC content, using adjusted least squares means, some significant interactions were noted between fish species and sites. PAHs were detected in aquatic animals at all sites (range of 0.017–17.534 μg/g ww), as were AHs (range of 0.423–4.549 μg/g ww); the highest levels of PAHs and AHs were found in bivalves from the Mississippi River. When analysis of variance (α = 0.05) was performed with data from aquatic animals, there were only two significant relationships between PAHs, AHs, and OCs between species, site, and age or the interaction among these variables. There was an interaction between fish species and n-decane (an AH) in that mullet and largemouth bass had significantly higher levels than did catfish ( P = 0.0175). When general linear means were used to investigate associations of inorganic contaminants among fish species, site, and age or any interactions among these variables, no significant results were noted for arsenic, cadmium, lead, beryllium, boron, molybdenum, or nickel. The range of mercury in fish in this study was 0.04–0.14 μg/g ww (0.14– 0.48 μg/g dry weight [dw]), with the most elevated levels detected in predatory largemouth bass at the sampling point farthest downstream from the structure and within the marsh area. Mercury was positively correlated with fish age ( P = 0.0152), where levels were estimated to increase 0.0253 parts per million (ppm) dw per year. In the Mississippi River, catfish showed significantly higher levels of mercury than did mullet or largemouth bass ( P = 0.00167). Among fish species, mullet displayed the highest levels in fish of aluminum, barium, manganese, and iron, all considered to have low toxicity in hydrologic systems. An interaction between fish and site was seen with aluminum ( P = 0.0031), where concentrations in mullet were significantly higher in the Mississippi River than at the other sites, as was also seen with barium ( P = 0.0009), chromium ( P = <0.0001), manganese ( P = 0.0004), strontium ( P = 0.0074), vanadium ( P = 0.0156), and zinc ( P = 0.0059). For iron ( P = 0.0.0001), mullet and largemouth bass at both the Mississippi River and Lake Salvador showed higher levels than did catfish, and these two species showed higher levels at two of the four sites. An interaction between fish and site was also seen with chromium ( P = <0.0001) in that concentrations in mullet were significantly higher in the Mississippi River than at the other sites, as was also seen with strontium ( P = 0.0074), vanadium ( P = 0.0156), and zinc ( P = 0.0059), metals for which deleterious effects have been demonstrated in other ecosystems. The NCBP program lists the 85th percentile for zinc at 34.2 μg/g fw (117.9 μg/g dw). In the Davis Pond prediversion biomonitoring study (hereafter the current study), one fish (MUL31RIVER, fish ID 8) showed values higher than that (125.4 μg/g dw or 37.54 μg/g ww), and the Mississippi River bivalve sample (MUSSRIVER) had a value of 140 μg/g dw (41.2 μg/g ww). In the current study, approximately 86 percent of the fish had measurable selenium levels, yet none reached the 85th percentile. The 85th percentile for selenium from the NCBP was 0.73 μg/g ww. Significantly higher levels of selenium were seen in mullet than in largemouth bass and catfish ( P = 0.0023). The NCBP 85th percentile for lead is 0.22 μg/g ww (0.76 μg/g dw). In the current study, the range of concentrations of lead was as much as 18.3 ppm dw (MUL31RIVER, fish ID 8), with the three most elevated values (range of 3.46–5.31 μg/g ww) coming from mullet from the Mississippi River. Biomarker data are measurable and directly reflect the condition of the animal, and measuring more than one biomarker in an individual increases confidence in health assessments. In the current study, biomarkers included macrophage aggregates (MAs), liver (hepatosomatic index [HSI]) and spleen (splenosomatic index [SSI]) weight to body weight ratios, percent white blood cells (WBCs) in whole blood, and condition factor. Few significant differences were noted with any of the biomarkers between sites, and there were no relationships between species and sites. For improved use of biomarker assessments, an increase in fish sample size would be useful for postdiversion sampling, as would comparisons of fish of the same sex and reproductive condition. During the current study, success for eagle nests in the diversion area and reference sites was similar as determined by numbers of nestlings fledged. When temperatures were below average during winter 2000, nests in both regions similarly failed. At each nest, the primary evidence of food items was small mammals. Eaglets (n = 6) generally appeared healthy, and whole blood concentrations of organic contaminants exceeded detection limits with three incidences of p,p’ -DDE (0.002–0.006 μg/L ww) and one incidence of oxychlordane (0.002 μg/L ww). The levels of p,p’ -DDE were well below those that have been inversely correlated with productivity and success rates of nesting bald eagles on a regional scale. The low values found in the whole blood samples for OC pesticides and PCBs were even lower when corrected for plasma volume. Aluminum values were 3.66 and 5.75 μg/L in two samples, zinc ranged from 5.21 to 6.77 μg/L ww in six samples, and silicon ranged from 1.7 to 4.6 μg/L in four samples. Selenium was detectable in each bird with the range at 0.332–0.566 μg/L ww, and strontium ranged from 0.0581 to 0.0975 μg/L ww. Mercury was detectable in blood samples from each bird and ranged from 0.0254 to 0.0845 μg/L ww, whereas lead was detectable in four samples and ranged from 0.0042 to 0.0136 μg/L ww. Although no detectable levels of total PCBs were found (also correlated with decreased reproductive productivity), 70 percent of the aquatic animals from the Mississippi River contained total PCBs (range 0.13–0.79 μg/L), whereas only about 7 percent of the aquatic animals sampled from the marsh area contained PCBs. Suggestions for postdiversion sampling include lowering the analytical detection limit for some metals, sampling aquatic animals over the course of a single season, obtaining a higher sample number of mature fish of one species (for example, blue catfish) within a range of total lengths for biomarker analyses, obtaining otoliths for estimating fish ages, assessing dioxins in eaglet blood, examining triazines in water, and obtaining all Mississippi River fish samples as close to the Davis Pond structure intake as possible. Because contaminants found in blood of eaglets reflect their prey species and because of the contaminant levels found in fish in the current study, eaglets may not be consuming primarily these species; therefore, obtaining juvenile nutria ( Myocastor coypus ) or turtle species for contaminant analyses might be considered, as well as collecting greater blood volume and using plasma to measure OCs and PCBs. Data obtained postdiversion will be compared with prediversion data to monitor changes.

Louisiana↗

USGS1998

Sponges of the Permian Upper Capitan Limestone Guadalupe Mountains, New Mexico and Texas

Demosponge "sphinctozoans" and inozoid calcareous sponges are major constituents of the Upper Permian, Upper Capitan Limestone in the Guadalupe Mountains of New Mexico and Texas. Systematic description, taxonomy, and the stratigraphic distribution of these sponges are documented in collections from exposures of the Upper Capitan Limestone in the vicinity of Carlsbad Caverns in New Mexico. The fauna appears diverse on a local scale, but when compared to diversity of assemblages of similar age in Tunisia and in Southern China, the assemblage is species poor, with 34 species of "calcareous" sponges and demosponges. Whether this is a local time or geographic gradient must wait additional investigations of sponge faunas from older parts of the Guadalupian series in the Guadalupe Mountains, as well as in localities southward in Texas and Mexico. Upper Capitan exposures near Carlsbad Caverns are at the northernmost end of the long Delaware Basin that was restricted by the Hovey channel to the south. As a consequence of either that restricted ecologic limitation or a time stratigraphic factor, Late Capitan assemblages are characterized by abundant individuals of only a few endemic species, and by relatively primitive cosmopolitan genera and species that were able to persist beyond the ranges of more specialized forms. Species in the collections include the ceractinomorphid porate "sphinctozoans" Cystothalamia guadalupensis (Girty, 1908a), Amblysiphonella cf. A. merlai Parona, 1933, Amblysiphonella species A, Amblysiphonella species B, Discosiphonella mammilosa (King, 1943), Tristratocoelia rhythmica Senowbari-Daryan and Rigby, 1988, Exaulipora permica (Senowbari-Daryan, 1990), type species of the new genus Exaulipora, Parauvanella minima Senowbari-Daryan, 1990, and Platythalamiella(?) sp., all from the families Sebargasiidae Steinmann, 1882, and Colospongiidae Senowbari-Daryan, 1990. The family Solenolmiidae Engeser, 1986 is represented by the new species Preverticillites parva. Among the ceractinomorphid Aporata, the family Thaumastocoeliidae Ott, 1967 is represented by Sollasia ostiolata Steinmann, 1882, and Girtyocoelia beedei (Girty, 1908b). The sclerospongiid Guadalupiidae Termier and Termier, in Termier, et al., 1977a, which includes the family Guadalupiidae Girty, 1908a, is represented by the species Guadalupia zitteliana Girty, 1908a, and Guadalupia explanata (King, 1943), Lemonea cylindrica (Girty, 1908a), Lemonea conica Senowbari-Daryan, 1990, Lemonea polysiphonata Senowbari-Daryan, 1990, and the new species Lemonea exaulifera and Lemonea micra. The Calcarea are represented within the subclass Aspiculata Rigby and Senowbari-Daryan, 1996a, and order Inozoida Rigby and Senowbari-Daryan, 1996a, by the Auriculospongiidae Termier and Termier, 1977a, which includes the large Gigantospongia discoforma Rigby and Senowbari-Daryan, 1996b. and Cavusonella caverna Rigby, Fan, and Zhang, 1989b. Also included are the Peronidellidae Wu, 1991, represented by the species Peronidella cf. P. rigbyi Senowbari-Daryan, 1991, Peronidella(?) delicata new species, and Minispongia constricta (Girty, 1908a), and the new genus and species Bicoelia guadalupensis. The family Virgulidae Termier and Termier, 1977a, is redefined to include the genus Virgola and the species Virgola neptunia (Girty, 1908a), and Virgola rigida (Girty, 1908a,). The family Polysiphonellidae Wu, 1991, (not Polysiphonellidae Belyaeva in Boiko, et al., 1991) is interpreted to include most of the subfamilies originally included by Rigby and Senowbari-Daryan (1996a) in the Virgulispongiidae. The sponge Grossotubinella parallela Rigby, Fan, and Zhang, 1989b is included there in the Preeudinae, with Pseudovirgula tenuis Girty, 1908a. Heliospongid demosponges are represented in the Upper Capitan by Heliospongia ramosa Girty, 1908b, Heliospongia vokesi King, 1943, and Neoheliospongia(?) cf. N. typica Deng, 1981. Fossils of unknown taxonomy, possibly sponges, hydrozoans or algae, are incl

Brigham Young University Geology Studies↗

USGS1995

Water-quality assessment of the Rio Grande Valley study unit, Colorado, New Mexico, and Texas -- Analysis of selected nutrient, suspended-sediment, and pesticide data

This report contains a summary of data compiled from sources throughout the Rio Grande Valley study unit of the National Water-Quality Assessment program. Information presented includes the sources and types of water-quality data available, the utility of water-quality data for statistical analysis, and a description of recent water-quality conditions and trends and their relation to natural and human factors. Water-quality data are limited to concentrations of selected nutrient species in surface water and ground water, concentrations of suspended sediment and suspended solids in surface water, and pesticides in surface water, ground water, and biota. The Rio Grande Valley study unit includes about 45,900 square miles in Colorado, New Mexico, and Texas upstream from the streamflow-monitoring station Rio Grande at El Paso, Texas. The area also includes the San Luis Closed Basin and the surface-water closed basins east of the Continental Divide and north of the United States-Mexico international border. The Rio Grande drains about 29,300 square miles in these States; the remainder of the study unit area is in closed basins. Concentrations of all nutrients found in surface-water samples collected from the Rio Grande, with the exception of phosphorus, generally remained nearly constant from the northernmost station in the study unit to Rio Grande near Isleta, where concentrations were larger by an order of magnitude. Total nitrogen and total phosphorus loads increased downstream between Lobatos, Colorado, and Albuquerque, New Mexico. Nutrient concentrations remained elevated with slight variations until downstream from Elephant Butte Reservoir, where nutrient concentrations were lower. Nutrient concentrations then increased downstream from the reservoir, as evidenced by elevated concentrations at Rio Grande at El Paso, Texas. Suspended-sediment concentrations were similar at stations upstream from Otowi Bridge near San Ildefonso, New Mexico. The concentration and estimated load were nearly two orders of magnitude larger at this station relative to upstream stations. Cochiti Lake allows suspended sediment to settle, thus the resulting concentration is substantially lower downstream from the reservoir. Downstream from Cochiti Lake, concentrations again increased due to inflow from tributaries, other ephemeral streams and arroyos, and agricultural and urban areas. Two ephemeral tributaries (Rio Puerco and Rio Salado, which are south of Albuquerque) contribute substantial amounts of suspended sediment to the Rio Grande. Suspended-sediment concentrations in the Rio Grande just downstream from Elephant Butte Dam decreased by nearly three orders of magnitude due to settling in the reservoir. Concentrations then increased due to agricultural and urban impacts downstream from the reservoir. Nutrients in ground water in the study unit do not appear to be a widespread problem. However, localized areas that have elevated nitrate concentrations have been documented. The largest median nitrate concentration was found in water from wells located in the Basin and Range-mountains-urban data stratum (3.0 milligrams per liter) and the smallest median nitrate concentration was found in water from wells located in the Southern Rocky Mountainsmountains-forest data stratum (0.08 milligram per liter). Few (3 percent) nitrate concentrations in water from wells in all data strata were greater than 10 milligrams per liter, and most (82 percent) were less than 2 milligrams per liter. Comparison of nitrate concentrations in water from wells located in specific land-use settings across all hydrogeologic settings, with the exception of the Colorado Plateau, indicated that the largest median nitrate concentration was associated with rangeland land use and that larger nitrate concentrations were found in water from shallow wells. Water from wells located in areas of rangeland land use consistently had larger median nutrient concentrations than water from wells in areas of other land uses. The largest median ammonia concentration was in water from wells located in the Colorado Plateau-San Juan Basin-rangeland data stratum (0.27 milligram per liter). Most median ammonia concentrations were less than 0.03 milligram per liter, indicating that elevated ammonia concentrations are not a major issue in the study unit. The largest median orthophosphate concentration was found in water from wells located in the Southern Rocky Mountains-mountains-forest data stratum (0.15 milligram per liter) and the smallest was found in water from wells located in the Basin and Range-mountains-urban data stratum (0.02 milligram per liter). Most orthophosphate concentrations (85 percent) sampled were less than 0.2 milligram per liter, indicating that elevated orthophosphate concentrations are not a major issue in the study unit. Pesticide analyses were available for only 38 ground-water sampling sites in the Rio Grande Valley study unit. Diazinon, at a concentration of 0.01 microgram per liter, was the only pesticide detected and it was detected at only one site. More study is needed to determine if pesticides are affecting ground-water quality in the Rio Grande Valley study unit. Surface-water biological pesticide data were inadequate for in-depth analysis. The primary sources of data were the U.S. Fish and Wildlife Service and the U.S. Geological Survey. In the U.S. Fish and Wildlife Service study p,p'-DDE, a degradation product of DDT, was detected most frequently; highest concentrations were found at Stahman Farms in carp (6.3 micrograms per gram wet-weight) and at Hatch in Western kingbird (5.1 micrograms per gram wet-weight). In the U.S. Geological Survey study of Bosque del Apache National Wildlife Refuge no detectable organochlorine concentrations were found in plants, but detectable levels of p,p'-DDE were found in coot and carp, with a maximum concentration of 0.12 microgram per gram wet-weight found in coot.

Colorado, New Mexico, Texas↗

USGS1985

Uranium mineralization in the Smith Lake district of the Grants uranium region, New Mexico.

The Mariano Lake and Ruby 1 uranium orebodies, which together comprise much of the uranium ore in the Smith Lake district of the Grants uranium region, New Mexico, occur in sandstones in the lower part of the Brushy Basin Member of the Upper Jurassic Morrison Formation. The orebodies, which are offset by faults of Laramide age, are enriched in an amorphous organic material that was introduced into the host sandstone after deposition. The enrichment by this organic material, in ore, is an important characteristic of the primary uranium deposits in the Grants uranium region. However, the close proximity of the chemically reduced ore zones to oxidized rock is suggestive that the deposits represent accumulations of uranium redistributed by reduction-oxidation processes from preexisting primary deposits.Within the ores, whole-rock abundances of organic carbon correlate positively with uranium contents. This correlation is consistent with petrologic evidence which indicates that uranium is everywhere intimately admixed with the amorphous organic material. Ore zones are also enriched in vanadium (as ore-stage vanadiferous chlorite) and sulfur (as ore-stage iron disulfide minerals with delta 34 S values ranging from -29 to -42ppm).Petrographic observations demonstrate that Smith Lake uranium mineralization occurred early (before major burial compaction) in the paragenetic sequence of host-rock diagenetic alterations but was preceded by precipitation of authigenic iron disulfides (delta 34 S values ranging from -11 to -38ppm), mixed-layered smectite-illite clays, and potassium feldspars.Additional preore alterations included dissolution of detrital sanidine and plagioclase and the leaching of iron from detrital iron-titanium oxide grains. Following mineralization, varying amounts of authigenic calcite and barite formed, both of which were partly replaced by kaolinitc. Oxidation of some previously formed iron disulfide minerals occurred late in the paragenetic sequence, as did localized precipitation of native selenium, pyrite, and very minor amounts of uranium minerals.The positive correlation between contents of uranium and organic carbon and the admixture of uranium with the amorphous organic material indicates that the Mariano Lake and Ruby 1 deposits are primary-type uranium orebodies. The offset of orebodies by Laramide faults and radiometric age determinations of the ores are also consistent with a primary origin for the deposits. Late Tertiary oxygenated ground waters locally modified original chemical and mineralogical characteristics of the ores in part by leaching some uranium. Secondary uranium minerals precipitated from the partly leached primary ores are sparse in the mine area; such recycled uranium appears to represent an insignificant proportion of the total uranium in the Smith Lake district.

Economic Geology↗

USGS1992

Organic matter diagenesis as the key to a unifying theory for the genesis of tabular uranium-vanadium deposits in the Morrison Formation, Colorado Plateau

Interstitial, epigenetic amorphous organic matter is intimately associated with uranium in the Grants uranium region on the southern part of the Colorado Plateau in northwestern New Mexico and is considered essential to genetic models for these deposits. In contrast, uranium minerals are intimately associated with authigenic vanadium chlorite and vanadium oxides in amorphous organic matter-poor ores of the Slick Rock and Henry Mountains mining districts on the northern part of the plateau, and therefore, in some genetic models amorphous organic matter is not considered crucial to the formation of these deposits. Differences in organic matter content can be explained by recognizing that amorphous organic matter-poor deposits have been subjected to more advanced stages of diagenesis than amorphous organic matter-rich deposits, during which organic compounds were broken down, solubilized, and removed during various diagenetic stages (e.g., sulfate reduction, methanogenesis, and organic acid production). Most diagenetic alterations (e.g., dissolution of framework grains and cements and precipitation of coarse-grained coffinite, vanadium clays, and vanadium oxides) characteristic of amorphous organic matter-poor deposits occurred when temperatures exceeded 80 degrees C--a temperature typical of the organic acid stage of diagenesis.Two factors combined to assure that a high percentage of the amorphous organic matter was removed from the Morrison Formation during diagenesis: the fact that the organic matter was humic (and therefore highly oxygenated), and that the juxtaposition of authigenic smectite and amorphous organic matter on grain rims facilitated clay mineral-organic catalysis reactions leading to the breakdown of large organic molecules into smaller, soluble molecules.Evidence that amorphous organic matter was involved in the genesis of organic matter-poor, as well as organic matter-rich, deposits includes the presence of leached iron-titanium oxides and strongly etched garnets (both attributed to leaching by organic acids), the gradation from organic matter-rich to organic matter-poor deposits in the Grants uranium region, the inverse correlation between the amount of amorphous organic matter and the intensity of diagenetic alteration, the ubiquitous occurrence of amorphous organic matter inclusions in coffinite, and the similarity in geometry of tabular uranium-vanadium ores and Holocene humate deposits. By recognizing that amorphous organic matter was crucial to the initial concentration of uranium (even in those deposits that presently contain little amorphous organic matter) and by recognizing the effects of the various stages of diagenesis on the ore, one genetic model may be applied to all of the sandstone-hosted, tabular-type uranium-vanadium deposits in the Morrison Formation on the Colorado Plateau.

Economic Geology↗

USGS2000

SHRIMP U-Pb zircon ages for Big Creek gneiss, Wyoming and Boulder Creek batholith, Colorado: Implications for timing of Paleoproterozoic accretion of the northern Colorado province

Sensitive, high-resolution, ion microprobe (SHRIMP) U-Pb zircon ages from a sample of the high-grade, hornblende-feldspathic Big Creek gneiss of the southeastern Sierra Madre, along with samples of a quartz monzonitic phase of the Boulder Creek batholith, help define timing of three major Paleoproterozoic thermo-tectonic events within the northern Colorado province at approximately 1810, 1710, and 1610 Ma. Previous ages determined for these key rock units were problematic; they hindered regional tectonic interpretations of the Paleoproterozoic crustal accretion history of the Colorado province that extends from the Cheyenne belt of southern Wyoming to north-central New Mexico. The Colorado province has been popularly modelled as a series of accreted oceanic volcano-plutonic arc systems and associated sediments, although alternative interpretations suggest that the series represents continental-margin arc rocks. The Big Creek gneiss has been interpreted as a high-grade basement equivalent of the oldest arc volcanic rocks exposed within the Green Mountain arc terrane, but it also has been suspected of being either an older block of pre-arc basement or perhaps an allochthonous piece of crust from slightly older orogens to the east and north. Previous ID-TIMS work on mg-size zircon fractions yielded U-Pb concordia upper-intercept ages of 1618 ± 22 and 1684 ± 5 Ma as well as negative lower-intercept ages, indicating complex U-Pb isotopic systematics involving at least two ages of zircon growth overprinted by at least one episode of Pb-loss. Zircons from this gneiss were analyzed using the SHRIMP, and a total of 32 spot analyses on both centers and rims produced a range of different 207 Pb/ 206 Pb ages between ∼1840 and ∼1560 Ma. The weighted mean of the oldest 207 Pb/ 206 Pb ages is 1812 ± 12 Ma and is interpreted to estimate the age of the protolith that appears to be slightly older than lower-grade metabasalts and associated plutons at ∼1790–1775 Ma. This protolith age of 1812 Ma further implies that significantly older crust (> 1820 Ma; e.g., Penokean orogeny) is not found in the Green Mountain magmatic arc. The youngest 207 Pb/ 206 Pb ages of ∼1610 Ma are interpreted to represent a time of new zircon growth during highly localized high-grade metamorphism—an event that also produced local granitic magmatism at ∼1625 Ma. The Boulder Creek batholith had been dated previously using the ID-TIMS, U-Pb zircon technique that yielded ages at ∼1670 and ∼1714 Ma, a 45-m.y. discrepancy that left the true age of the batholith in doubt. Zircons from two samples, previously dated using the ID-TIMS method, were analyzed using SHRIMP, and yielded concordia upper-intercept ages of 1713 ± 10 and 1721 ± 15 Ma. These results, combined with two earlier U-Pb zircon determinations, help to establish the age of the Boulder Creek batholith at 1714.4 ± 4.6 Ma (weighted mean), an age more compatible with those for the other large, tonalitic to quartz monzonitic, syntectonic plutons within the northern Colorado province. The new Boulder Creek age helps to establish a discrete period of plutonism (∼1735–1705 Ma) that is syn- to post-tectonic with respect to major regional structures of deformation and metamorphism in the northern Colorado province. Assuming the multiple oceanic arc accretion model, the new age for the mid-crustal emplacement of this batholith into a deforming composite back-arc basin may date the closure of that basin during crustal shortening.

Colorado, Wyoming↗

USGS2025

Depth of magma crystallization and fluid exsolution beneath the porphyry-skarn Cu deposits at Santa Rita and Hanover-Fierro, New Mexico, USA

The depth level at which porphyry Cu–forming magmas fractionated and exsolved mineralizing fluids is actively debated. In the classic model, extensive magma fractionation occurs in large, upper crustal magma chambers, and concomitant fluid exsolution leads to forceful expulsion of residual magmas in the form of porphyry dikes, stocks, and breccia pipes, which subsequently serve as pathways for the mineralizing fluids. In contrast, some recent studies highlighting the role of deep crustal magma fractionation in the production of fertile magmas essentially deny the existence of upper crustal magma chambers at the time of mineralization. To address this, we conducted a detailed thermobarometric investigation of 13 intermediate to felsic, porphyritic intrusive rocks related to porphyry-skarn Cu mineralization at Santa Rita and Hanover-Fierro, New Mexico, United States, representing two premineralization magmas (61–60 Ma), seven synmineralization magmas (60–58 Ma), and four late- to postmineralization magmas (58–57 Ma). For each sample, the pressure of last magma crystallization before final magma ascent to the current exposure level was reconstructed based on Al-in-hornblende barometry of small hornblende inclusions trapped within quartz phenocrysts and through titanium-in-quartz (TitaniQ) thermobarometry of the host quartz phenocrysts themselves. Since quartz is one of the last crystallizing magmatic minerals, and no significant phenocryst growth could have occurred in small dikes and stocks after final magma emplacement, quartz phenocrysts and their contained hornblende inclusions record the depth of last magma crystallization before final magma ascent. When present, hornblende phenocrysts and hornblende inclusions within other major phenocrysts were also analyzed. Both quartz and hornblende barometers return consistent average pressures of 3.2 ± 0.4 kbar for the entire suite of pre- to postmineralization magmas, corresponding to depths of 11 to 14 km. The synmineralization magmas return even more consistent average pressures of 3.1 ± 0.2 kbar, corresponding to a depth of 12 ± 1 km. The volume of the mineralizing porphyry dikes and stocks at the emplacement level is far too small to have provided all the fluids and metals required to form the observed ore deposits. Therefore, the majority of the ore-forming fluids must have originated from the magmas that crystallized at 12 ± 1 km depth. The ore deposits, conversely, formed at ~5-km paleodepth. This implies that most of the mineralizing fluids traveled an average vertical distance of ~7 km from their magmatic source to the eventual site of ore precipitation. The relatively unaltered nature and low veining degree of deeper parts of mineralized porphyry dikes and stocks suggest that the fluid transport through these intrusive bodies occurred mostly at near-solidus conditions by means of fluid percolation along grain boundaries. In summary, our results suggest that (1) a large, upper crustal pluton exists ~7 km beneath the Santa Rita and Hanover-Fierro deposits; (2) abundant phenocryst crystallization occurred at this depth level; and (3) this pluton was the main source for the exsolution of ore-forming fluids. However, the investigated rocks have elevated whole-rock Sr/Y ratios, indicating magma fractionation at deep crustal levels. As a result, our preferred model is a combination of the two end-member models introduced above, with most magma fractionation having occurred in the deep crust and with residual, intermediate to felsic melts having ascended and accumulated at 11 to 14 km paleodepth, where they continued to crystallize with comparatively little crystal-liquid separation, before some of these magmas ascended further to shallow levels and quenched to porphyries.

New Mexico↗

USGS2017

Fluorine

Fluorine compounds are essential in numerous chemical and manufacturing processes. Fluorspar is the commercial name for fluorite (isometric CaF 2 ), which is the only fluorine mineral that is mined on a large scale. Fluorspar is used directly as a fluxing material and as an additive in different manufacturing processes. It is the source of fluorine in the production of hydrogen fluoride or hydrofluoric acid, which is used as the feedstock for numerous organic and inorganic chemical compounds. The United States was the world’s leading producer of fluorspar until the mid-1950s. In the mid-1970s, the U.S. fluorspar mining industry began to decline because of foreign competition. By 1982, there was essentially only a single U.S. producer left, and that company ceased mining in 1996. Consumption of fluorspar in the United States peaked in the early 1970s, which was also the peak period of U.S. steel production. Since then, U.S. fluorspar consumption has decreased substantially; the United States has nonetheless increased its imports of downstream fluorine compounds, such as, in order of tonnage imported, hydrofluoric acid, aluminum fluoride, and cryolite. This combination of no U.S. production (until recently) and high levels of consumption has made the United States the world’s leading fluorspar-importing country, in all its various forms. The number of fluorspar-exporting countries has decreased substantially in recent decades, and, as a result, the United States has become dependent on just a few countries to supply its needs. In 2013, the United States imported the majority of its fluorspar from three countries, which were, in descending order of the amount imported, Mexico, China, and South Africa. Geologically, in igneous systems, fluorine is one of a number of elements that are “incompatible.” These incompatible elements become concentrated in the residual magma while the common silicates crystallize upon magma ascent and cooling, leading to relatively high fluorine concentrations in the more evolved or differentiated igneous rocks and in hydrothermal deposits associated with those evolved igneous rocks. In sedimentary rocks, fluorine’s highest concentrations are found in phosphorites because fluorine substitutes for hydroxyl ions in apatite, which leads to fluorine concentrations of, typically, from 2 to 4 weight percent in phosphorites. Because of the presence of fluorine, phosphate fertilizer manufacturers can produce a fluorosilicic acid byproduct. Most deposits mined for fluorine are hydrothermal, however, and consist of fluorine minerals that precipitated from hot water. Magmatic brines and brines from deep within sedimentary basins that have high concentrations of dissolved fluoride are the mineralizing fluids for various types of hydrothermal fluorspar deposits. Relatively dilute hydrothermal fluids that formed in some volcanic rocks can also transport sufficient fluoride to form a high-grade fluorspar deposit. Fluorite has low solubility in a common range of hydrothermal temperatures, particularly from about 160 degrees Celsius (°C) down to 60 °C. The increasing fluorite solubility below 60 °C partly explains why some water with exceptionally high levels of dissolved fluorine are found even at ambient temperatures in evaporitic lake basins in some East African Rift valleys in Kenya and Tanzania. The geologic conditions that led to the high concentrations there are known to exist in a number of other places in the world as well, including, perhaps, places in the Basin and Range province of the United States. Eight minerals or mineral groups have sufficient fluorine in their structures to be considered as possible ores of the element; they are bastnaesite (also spelled bastnäsite; and other fluorocarbonates), cryolite, sellaite, villiaumite, fluorite, fluorapatite (in phosphorites), various phyllosilicates, and topaz. Fluorite is currently the only mineral that is mined for fluorine, and nomineral except fluorite is likely to become a source of commercially produced fluorine as a primary product as long as supplies from relatively thick and high-grade fluorite deposits continue to be available. At least seven classes (which include one subclass) of hydrothermal fluorite deposits are recognized; they are classified according to their tectonic and (or) magmatic settings, as follows: (1) carbonatite-related fluorspar deposits; (2) alkaline-intrusion-related fluorspar deposits; (3) alkaline-volcanic-related epithermal fluorspar deposits; (4) Mississippi Valley-type fluorspar deposits (and a subclass of salt-related carbonate-hosted fluorspar deposits); (5) fluorspar deposits related to strongly differentiated granites; (6) subalkaline-volcanic-related epithermal fluospar deposits; and (7) fluorspar deposits that appear to be conformable within tuffaceous limy lacustrine sediments. An eighth class (not hydrothermal) is that of fluorspar deposits concentrated in soils and weathered zones; that is, residual fluorspar deposits. Generally, fluorspar deposits related to strongly differentiated granites have larger tonnages and lower grades than carbonatite-related fluorspar deposits, which, in turn, have larger tonnages and lower grades than fluorspar vein deposits from various other classes. The United States has a few identified resources of fluorspar, most notably the Klondike II property in the Illinois- Kentucky fluorspar district located about 8 kilometers southwest of Salem, Kentucky, which has a large vein that contains at least 1.6 million metric tons at a grade of 60 percent CaF 2 (Feytis, 2009). Additional fluorspar resources of lower grade but larger tonnage have been identified at Hicks Dome in the Illinois-Kentucky fluorspar district and at Lost River near the western tip of the Seward Peninsula in Alaska, along with a couple of dozen smaller, higher grade resources. Internationally, new mines that either opened before the beginning of 2013 or were scheduled to open soon after that time include the Nui Phao tungsten-fluorspar-bismuth-copper-gold deposit in northern Vietnam; the St. Lawrence project in Newfoundland, Canada, which is located in a well-known fluorspar district; the Bamianshan deposit, which is related to a strongly differentiated granite in northwestern Zhejiang Province, China, near some of that Province’s large, subalkaline-volcanic-related epithermal veins; and the Nokeng project in South Africa, which is also related to a strongly differentiated granite. Other deposits in northwestern Australia, Nevada (United States), Norway, South Africa, and Sweden have been identified and could be put into production within just a few years. Among undiscovered resources, an interesting possibility might be to produce a fluorine product from evaporitic, high-fluorine, high-pH sodium-carbonate brines like Lake Magadi (Kenya) and Lake Natron (Tanzania) in Africa’s Eastern Rift Valley. In addition, apparently conformable fluorspar deposits in tuffaceous limy lacustrine sediments, such as those in Italy, are likely to occur in similar young alkalic volcanic settings elsewhere in the world. Modern geophysical and geochemical exploration techniques have typically not been brought to bear in exploration for new fluorspar deposits, although such techniques are likely to be used in future exploration. The tendency for fluorine to dissolve in significant concentrations in water at low temperature allows both surface water and groundwater to be used as sampling media in geochemical exploration. Evolved granite-related fluorspar deposits may be particularly susceptible to geophysical exploration methods because crystalline rocks that form a basement to sedimentary sections can be approximately defined with gravity and magnetic methods, and magnetite-bearing skarns can be directly detected with magnetic surveys. Environmental considerations of fluorine mining focus especially on drinking water, where high fluorine concentrations can lead to tooth decay; dental and skeletal fluorosis; and bone and cartilage conditions, including genu valgum, which is the crippling bone deformity more commonly known as knock knee. Trace amounts of other elements in fluorspar ores are a concern at some deposits; for example, high beryllium concentrations in alkaline-volcanic-related epithermal deposits or high cadmium concentrations associated with Mississippi Valley-type and salt-related carbonate-hosted fluorspar deposits. Future research might include testing whether fluorine can be extracted economically from high-pH, sodium-carbonate brines and exploring for new occurrences of apparently conformable fluorspar deposits in tuffaceous limy lacustrine sediments outside of the Latium Region of Italy. Other promising new areas of research could be studies of fluorspar deposit fluid inclusion compositions by quadrupole mass spectrometry, by noble gas mass spectrometry on irradiated fluid inclusions, or by chlorine isotopes, while also measuring the chemistry of the same fluid inclusions either by bulk crush-and-leach methods or by laser ablation-inductively coupled plasma mass spectrometry. Advanced studies of fluid inclusion chemistry could be applied beneficially to some of the enigmatic large epithermal fluorspar veins at various places in the world, where they might determine those deposits’ possible relationships to igneous intrusions, or to dissolved salt, or to heated meteoric water in volcanic sections, or perhaps to all three. This knowledge could help focus new exploration.

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