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Gary P. Landis

Publications and source records attributed to Gary P. Landis.

12 recordsLinked to original sources
USGS2022

40Ar/39Ar geochronology of magmatic-steam alunite from Alunite Ridge and Deer Trail Mountain, Marysvale Volcanic Field, Utah: Timing and duration of miocene hydrothermal activity associated with concealed intrusions

Porphyry and epithermal deposits are important sources of base and precious metals. Most actively mined deposits have been exhumed such that ore bodies are relatively close to the surface and are therefore locatable and economic to extract. Identifying and characterizing concealed deposits, particularly more deeply buried porphyry deposits, represents a far greater challenge for mineral exploration, and will become progressively more important as near-surface resources are gradually exhausted over time. We report high-precision 40 Ar/ 39 Ar dates for coarsely crystalline alunite that precipitated from magmatic steam in open fractures in Oligocene dacitic volcanic rocks, and a SHRIMP 206 Pb/ 238 U zircon date for one of several rhyolite dikes present at Alunite Ridge and Deer Trail Mountain, Utah. Both the magmatic-steam alunite and rhyolite dikes are related to concealed intrusions. The rhyolite dike yielded an age of 30.72 ± 0.36 Ma, which is older than a commonly cited 27.1 Ma age estimate for the Three Creeks Tuff Member of the Bullion Canyon Volcanics that is cut by the dike. 40 Ar/ 39 Ar data for samples of magmatic-steam alunite and sericite from six mines and prospects provide evidence for at least two periods of episodic hydrothermal activity at ca. 15.7–15.1 Ma and ca. 14.7–13.8 Ma, with the older and younger pulses of activity recorded at the more eastern and western sites, respectively. These two periods of hydrothermal activity are consistent with previous interpretations that Alunite Ridge and Deer Trail Mountain are underlain by two concealed porphyry stocks. 40 Ar/ 39 Ar analyses of individual bands in a sample of massive, centimeter-scale banded vein alunite yield indistinguishable ages with a weighted mean of 13.98 ± 0.12 Ma, consistent with a short-lived (≲250 ka) magmatic event with episodic vapor discharge recurring on short timescales (≲36 ka). 40 Ar/ 39 Ar geochronology of magmatic-steam alunite is a valuable tool to constrain the timing and duration of magmatic hydrothermal activity associated with unexposed intrusions and potentially porphyry deposits, and therefore may be useful in exploration.

Utah↗
USGS2016

Groundwater ages from the freshwater zone of the Edwards aquifer, Uvalde County, Texas—Insights into groundwater flow and recharge

Tritium–helium-3 groundwater ages of the Edwards aquifer in south-central Texas were determined as part of a long-term study of groundwater flow and recharge in the Edwards and Trinity aquifers. These ages help to define groundwater residence times and to provide constraints for calibration of groundwater flow models. A suite of 17 samples from public and private supply wells within Uvalde County were collected for active and noble gases, and for tritium–helium-3 analyses from the confined and unconfined parts of the Edwards aquifer. Samples were collected from monitoring wells at discrete depths in open boreholes as well as from integrated pumped well-head samples. The data indicate a fairly uniform groundwater flow system within an otherwise structurally complex geologic environment comprised of regionally and locally faulted rock units, igneous intrusions, and karst features within carbonate rocks. Apparent ages show moderate, downward average, linear velocities in the Uvalde area with increasing age to the east along a regional groundwater flow path. Though the apparent age data show a fairly consistent distribution across the study area, many apparent ages indicate mixing of both modern (less than 60 years) and premodern (greater than 60 years) waters. This mixing is most evident along the “bad water” line, an arbitrary delineation of 1,000 milligrams per liter dissolved solids that separates the freshwater zone of the Edwards aquifer from the downdip saline water zone. Mixing of modern and premodern waters also is indicated within the unconfined zone of the aquifer by high excess helium concentrations in young waters. Excess helium anomalies in the unconfined aquifer are consistent with possible subsurface discharge of premodern groundwater from the underlying Trinity aquifer into the younger groundwater of the Edwards aquifer.

Texas↗
USGS2013

Ore genesis constraints on the Idaho cobalt belt from fluid inclusion gas, noble gas isotope, and ion ratio analyses--a reply

Burlinson (2013) questions the veracity of the H 2 concentrations reported for fluid inclusion extracts from minerals in the Idaho cobalt belt (Table 2; Landis and Hofstra, 2012) and suggests that they are an analytical artifact of electron-impact mass spectrometry. He also declares that H 2 should not be present in fluid inclusions because it is invariably lost by diffusion and is never detected in fluid inclusions by laser Raman. We welcome this opportunity to reply and maintain that the reported H 2 contents are accurate. Below we explain why Burlinson’s criticisms are invalid.

Idaho↗
USGS2013

Mass fractionation of noble gases in synthetic methane hydrate: Implications for naturally occurring gas hydrate dissociation

As a consequence of contemporary or longer term (since 15 ka) climate warming, gas hydrates in some settings may presently be dissociating and releasing methane and other gases to the ocean-atmosphere system. A key challenge in assessing the impact of dissociating gas hydrates on global atmospheric methane is the lack of a technique able to distinguish between methane recently released from gas hydrates and methane emitted from leaky thermogenic reservoirs, shallow sediments (some newly thawed), coal beds, and other sources. Carbon and deuterium stable isotopic fractionation during methane formation provides a first-order constraint on the processes (microbial or thermogenic) of methane generation. However, because gas hydrate formation and dissociation do not cause significant isotopic fractionation, a stable isotope-based hydrate-source determination is not possible. Here, we investigate patterns of mass-dependent noble gas fractionation within the gas hydrate lattice to fingerprint methane released from gas hydrates. Starting with synthetic gas hydrate formed under laboratory conditions, we document complex noble gas fractionation patterns in the gases liberated during dissociation and explore the effects of aging and storage (e.g., in liquid nitrogen), as well as sampling and preservation procedures. The laboratory results confirm a unique noble gas fractionation pattern for gas hydrates, one that shows promise in evaluating modern natural gas seeps for a signature associated with gas hydrate dissociation.

Chemical Geology↗
USGS2012

Ore genesis constraints on the Idaho Cobalt Belt from fluid inclusion gas, noble gas isotope, and ion ratio analyses

The Idaho cobalt belt is a 60-km-long alignment of deposits composed of cobaltite, Co pyrite, chalcopyrite, and gold with anomalous Nb, Y, Be, and rare-earth elements (REEs) in a quartz-biotite-tourmaline gangue hosted in Mesoproterozoic metasedimentary rocks of the Lemhi Group. It is the largest cobalt resource in the United States with historic production from the Blackbird Mine. All of the deposits were deformed and metamorphosed to upper greenschist-lower amphibolite grade in the Cretaceous. They occur near a 1377 Ma anorogenic bimodal plutonic complex. The enhanced solubility of Fe, Co, Cu, and Au as chloride complexes together with gangue biotite rich in Fe and Cl and gangue quartz containing hypersaline inclusions allows that hot saline fluids were involved. The isotopes of B in gangue tourmaline are suggestive of a marine source, whereas those of Pb in ore suggest a U ± Th-enriched source. The ore and gangue minerals in this belt may have trapped components in fluid inclusions that are distinct from those in post-ore minerals and metamorphic minerals. Such components can potentially be identified and distinguished by their relative abundances in contrasting samples. Therefore, we obtained samples of Co and Cu sulfides, gangue quartz, biotite, and tourmaline and post-ore quartz veins as well as Cretaceous metamorphic garnet and determined the gas, noble gas isotope, and ion ratios of fluid inclusion extracts by mass spectrometry and ion chromatography. The most abundant gases present in extracts from each sample type are biased toward the gas-rich population of inclusions trapped during maximum burial and metamorphism. All have CO 2 /CH 4 and N 2 /Ar ratios of evolved crustal fluids, and many yield a range of H 2 -CH 4 -CO 2 -H 2 S equilibration temperatures consistent with the metamorphic grade. Cretaceous garnet and post-ore minerals have high R H and R S values suggestive of reduced sulfidic conditions. Most extracts have anomalous 4 He produced by decay of U and Th and 38 Ar produced by nucleogenic production from 41 K. In contrast, some ore and gangue minerals yield significant SO 2 and have low R H and R S values of a more oxidized fluid. Three extracts from gangue quartz have high helium R/R A values indicative of a mantle source and neon isotope compositions that require nucleogenic production of 22 Ne in fluorite from U ± Th decay. Two extracts from gangue quartz have estimated 40 K/ 40 Ar that permit a Precambrian age. Extracts from gangue quartz in three different ore zones are biased toward the hypersaline population of inclusions and have a tight range of ion ratios (Na, K, NH 4 , Cl, Br, F) suggestive of a single fluid. Their Na, Cl, Br ratios suggest this fluid was a mixture of magmatic and basinal brine. Na-K-Ca temperatures (279°–347°C) are similar to homogenization temperatures of hypersaline inclusions. The high K/Na of the brine may be due to albitization of K silicate minerals in country rocks. Influx of K-rich brines is consistent with the K metasomatism necessary to form gangue biotite with high Cl. An extract from a post-ore quartz vein is distinct and has Na, Cl, Br ratios that resemble metamorphic fluids in Cretaceous silver veins of the Coeur d’Alene district in the Belt Basin. The results show that in some samples, for certain components, it is possible to “see through” the Cretaceous metamorphic overprint. Of great import for genetic models, the volatiles trapped in gangue quartz have 3 He derived from a mantle source and 22 Ne derived from fluorite, both of which may be attributed to nearby ~1377 Ma basalt-rhyolite magmatism. The brine trapped in gangue quartz is a mixture of magmatic fluid and evaporated seawater. The former requires a granitic intrusion that is present in the bimodal intrusive complex, and the latter equatorial paleolatitudes that existed in the Mesoproterozoic. The results permit genetic models involving heat and fluids from the neighboring bimodal plutonic complex and convection of basinal brine in the Lemhi Group. While the inferred fluid sources in the Idaho cobalt belt are similar in many respects to those in iron oxide copper-gold deposits, the fluids were more reduced such that iron was fixed in biotite and tourmaline instead of iron oxides.

Idaho↗
USGS2012

The Spar Lake strata-Bound Cu-Ag deposit formed across a mixing zone between trapped natural gas and metals-bearing brine

Ore formation at the Spar Lake red bed-associated strata-bound Cu deposit took place across a mixing and reaction zone between a hot oxidized metals-transporting brine and a reservoir of “sour” (H 2 S-bearing) natural gas trapped in the host sandstones. Fluid inclusion volatile analyses have very high CH 4 concentrations (≥1 mol % in most samples), and a sample from the fringe of the deposit has between 18 and 36 mol % CH 4 . The ratio of CH 4 /CO 2 in fluid inclusions appears to vary regularly across the deposit, with the lowest CH 4 /CO 2 ratios from high-grade chalcocite-bearing ore, and the highest from the chalcopyrite-bearing fringe. The helium R/R a isotope ratios (0.23–0.98) and concentrations define a mixture between crustal and atmospheric helium. The volatiles in fluid inclusions (CH 4 , CO 2 , H 2 S, SO 2 , H 2 , H 2 O, and other organic gases) and values of f O 2 and temperature calculated from the volatiles data all show gradations across the deposit that are completely consistent with such a mixing and reaction zone. Other volatiles from the fluid inclusions (HCl, HF, 3 He, Msup>4 He, N 2 , Ar) characterize the brine and give evidence for only shallow crustal fluids with no magmatic influences. The brine entered the gas reservoir from below and along the axis of the deposit and migrated out along bedding to the southwest, northeast, and northwest. Metals-transporting brines may have been fed into the host sandstones from the East Fault, but that remains uncertain. Abundant ore-stage Fe and Mn calcite cements from the reduced fringe have δ 13 C values as low as −18.4‰, and many values less than −10‰, which indicate that significant carbonate was generated by oxidation of organic carbon from the natural gas. The zone of calcite cements with very low δ 13 C values approximately envelopes chalcocite-bearing ore. Sulfur isotope data of Cu, Pb, and Fe sulfides and barite indicate derivation of roughly half of the orebody sulfide directly from sour gas H 2 S. That sour gas H 2 S had developed in steps known from other sedimentary basins, starting with (1) bacterial sulfate reduction (BSR) of seawater sulfate having δ 34 S of about 20‰ and sequestering of the sulfide in organic matter in source rocks stratigraphically below the deposit host rocks, followed by (2) maturation of the sulfide-bearing organic matter into liquid petroleum with relatively homogeneous sulfide having δ 34 S of 5 ± 5‰, then by (3) thermal cracking of the oil to CH 4 and H 2 S with relatively homogeneous sulfide having δ 34 S closely distributed, about 6‰. The CH 4 and H 2 S migrated and were trapped in sandstones of the upper member of the Revett Formation, where they were later met by the 200°C metals-transporting brine. There was additional contribution of sulfide to ore from later thermochemical sulfate reduction (TSR) operating on sulfate δ 34 S of 20 to 29‰ in both formation waters and metals-transporting solutions. A large range of δ 34 S in sulfides resulted as the 6‰ sour gas sulfide was supplemented with varying proportions of 20 to 29‰ sulfide from TSR.

Economic Geology↗
USGS2011

Observations of mass fractionation of noble gases in synthetic methane hydrate

As a consequence of contemporary or longer term (since 15 ka) climate warming, gas hydrates in some settings are presently dissociating and releasing methane and other gases to the oceanatmosphere system. A key challenge in assessing the susceptibility of gas hydrates to warming climate is the lack of a technique able to distinguish between methane recently released from gas hydrates and methane emitted from leaky thermogenic reservoirs, shallow sublake and subseafloor sediments, coalbeds, and other sources. Carbon and deuterium stable isotopic data provide only a first-order characterization of methane sources, while gas hydrate can sequester any type of methane. Here, we investigate the possibility of exploiting the pattern of noble gas fractionation within the gas hydrate lattice to fingerprint methane released from gas hydrates. Starting with synthetic gas hydrate formed under careful laboratory conditions, we document complex noble gas fractionation patterns in the gases liberated during dissociation and explore the effects of aging and storage (e.g., in liquid nitrogen), as well as sampling and preservation procedures. The laboratory results confirm a unique noble gas fractionation pattern for gas hydrates, one that shows promise in evaluating modern natural gas seeps for a signature associated with gas hydrate dissociation.

Conference Paper↗
USGS2010

Evolution of Ore Deposits and Technology Transfer Project: Isotope and Chemical Methods in Support of the U.S. Geological Survey Science Strategy, 2003-2008

Principal functions of the U.S. Geological Survey (USGS) Mineral Resources Program are providing assessments of the location, quantity, and quality of undiscovered mineral deposits, and predicting the environmental impacts of exploration and mine development. The mineral and environmental assessments of domestic deposits are used by planners and decisionmakers to improve the stewardship of public lands and public resources. Assessments of undiscovered mineral deposits on a global scale reveal the potential availability of minerals to the United States and other countries that manufacture goods imported to the United States. These resources are of fundamental relevance to national and international economic and security policy in our globalized world economy. Performing mineral and environmental assessments requires that predictions be made of the likelihood of undiscovered deposits. The predictions are based on geologic and geoenvironmental models that are constructed for the diverse types of mineral deposits from detailed descriptions of actual deposits and detailed understanding of the processes that formed them. Over the past three decades the understanding of ore-forming processes has benefited greatly from the integration of laboratory-based geochemical tools with field observations and other data sources. Under the aegis of the Evolution of Ore Deposits and Technology Transfer Project (referred to hereinafter as the Project), a 5-year effort that terminated in 2008, the Mineral Resources Program provided state-of-the-art analytical capabilities to support applications of several related geochemical tools to ore-deposit-related studies. The analytical capabilities and scientific approaches developed within the Project have wide applicability within Earth-system science. For this reason the Project Laboratories represent a valuable catalyst for interdisciplinary collaborations of the type that should be formed in the coming years for the United States to meet its natural-resources and natural-science needs. This circular presents an overview of the Project. Descriptions of the Project laboratories are given first including descriptions of the types of chemical or isotopic analyses that are made and the utility of the measurements. This is followed by summaries of select measurements that were carried out by the Project scientists. The studies are grouped by science direction. Virtually all of them were collaborations with USGS colleagues or with scientists from other governmental agencies, academia, or the private sector.

Circular↗
USGS1988

Gas bubbles in fossil amber as possible indicators of the major gas composition of ancient air

Gases trapped in Miocene to Upper Cretaceous amber were released by gently crushing the amber under vacuum and were analyzed by quadrupole mass spectrometry. After discounting the possibility that the major gases N 2 , O 2 , and CO 2 underwent appreciable diffusion and diagenetic exchange with their surroundings or reaction with the amber, it has been concluded that in primary bubbles (gas released during initial breakage) these gases represent mainly original ancient air modified by the aerobic respiration of microorganisms. Values of N 2 /(CO 2 + O 2 ) for each time period give consistent results despite varying O 2 /CO 2 ratios that presumably were due to varying degrees of respiration. This allows calculation of original oxygen concentrations, which, on the basis of these preliminary results, appear to have changed from greater than 30 percent O 2 during one part of the Late Cretaceous (between 75 and 95 million years ago) to 21 percent during the Eocene-Oligocene and for present-day samples, with possibly lower values during the Oligocene-Early Miocene. Variable O 2 levels over time in general confirm theoretical isotope-mass balance calculations and suggest that the atmosphere has evolved over Phanerozoic time.

Science↗