Search USGS⌕ Search

USGS · 70017615

Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona

Abstract

Thousands of solution-collapse breccia pipes crop out in the canyons and on the plateaus of northwestern Arizona; some host high-grade uranium deposits. The mineralized pipes are enriched in Ag, As, Ba, Co, Cu, Mo, Ni, Pb, Sb, Se, V and Zn. These breccia pipes formed as sedimentary strata collapsed into solution caverns within the underlying Mississippian Redwall Limestone. A typical pipe is approximately 100 m (300 ft) in diameter and extends upward from the Redwall Limestone as much as 1000 m (3000 ft). Unmineralized gypsum and limestone collapses rooted in the Lower Permian Kaibab Limestone or Toroweap Formation also occur throughout this area. Hence, development of geochemical tools that can distinguish these unmineralized collapse structures, as well as unmineralized breccia pipes, from mineralized breccia pipes could significantly reduce drilling costs for these orebodies commonly buried 300–360 m (1000–1200 ft) below the plateau surface. Design and interpretation of soil sampling surveys over breccia pipes are plagued with several complications. (1) The plateau-capping Kaibab Limestone and Moenkopi Formation are made up of diverse lithologies. Thus, because different breccia pipes are capped by different lithologies, each pipe needs to be treated as a separate geochemical survey with its own background samples. (2) Ascertaining true background is difficult because of uncertainties in locations of poorly-exposed collapse cones and ring fracture zones that surround the pipes. Soil geochemical surveys were completed on 50 collapse structures, three of which are known mineralized breccia pipes. Each collapse structure was treated as an independent geochemical survey. Geochemical data from each collapse feature were plotted on single-element geochemical maps and processed by multivariate factor analysis. To contrast the results between geochemical surveys (collapse structures), a means of quantifying the anomalousness of elements at each site was developed. This degree of anomalousness, named the “correlation value”, was used to rank collapse features by their potential to overlie a deeply-buried mineralized breccia pipe. Soil geochemical results from the three mineralized breccia pipes (the only three of the 50 that had previously been drilled) show that: (1) Soils above the SBF pipe contain significant enrichment of Ag, Al, As, Ba, Ga, K, La, Mo, Nd, Ni, Pb, Sc, Th, U and Zn, and depletion in Ca, Mg and Sr, in contrast to soils outside the topographic and structural rim; (2) Soils over the inner treeless zone of the Canyon pipe show Mo and Pb enrichment anf As and Ga depletion, in contrast to soils from the surrounding forest; and (3) The soil survey of the Mohawk Canyon pipe was a failure because of the rocky terrane and lack of a B soil horizon, or because the pipe plunges. At least 11 of the 47 other collapse structures studied contain anomalous soil enrichments similar to the SBF uranium ore-bearing pipe, and thus have good potential as exploration targets for uranium. One of these 11, #1102, does contain surface mineralized rock. These surveys suggest that soil geochemical sampling is a useful tool for the recognition of many collapse structures with underlying ore-bearing breccia pipes.

Explore related subjects

90° N90° S · 180° W ← longitude → 180° E
Source-reported bounding extent: 35.60134849448217° to 36.43233656059891° latitude; -114.31581652045145° to -112.90029352070502° longitude. This indicates report coverage, not an exact sampling location. View area on OpenStreetMap.

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

K. J. Wenrich, R. M. Aumente-Modreski. 1994. Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona. https://doi.org/10.1016/0883-2927(94)90065-5

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Elemental and isotope geochemistry of Smackover Formation brines in Alabama and Arkansas: Implications for fluid mixing and water-rock interaction

This study investigates the geochemical characteristics of brines within the Upper Jurassic Smackover Formation in Alabama and Arkansas through elemental and isotopic analyses and geochemical modeling to reveal the extent and nature of fluid mixing and water-rock interactions. Smackover Formation brines exhibit Na-Cl-Ca hydrogeochemical facies and sulfate depletion relative to seawater. Lower sulfate concentrations, coupled with high H 2 S concentrations in some brines (0-364 mg/L) at temperatures >80°C, suggest that thermochemical sulfate reduction occurred. Cl/Br and Na/Br ratios indicate that salinity was controlled by the mixing of meteoric water with evaporated seawater that had reached halite saturation, rather than by halite dissolution. The δ 18 O and δ 2 H values of the brines also suggest mixing between meteoric water and evaporated seawater that had reached gypsum and halite saturation. Geochemical modeling of seawater evaporation predicts a Cl-Na or Cl-Mg facies after halite saturation, contrasting with the observed Cl-Ca dominance of the Smackover Formation brines. The Ca-enriched brines may have evolved from Cl-Mg-dominated evaporated seawater through dolomitization of limestone. The 87 Sr/ 86 Sr ratios range from 0.70740 to 0.71048, higher than the average of Jurassic seawater (0.707). The non-linear relationship between 87 Sr/ 86 Sr and 1000/Sr suggests alteration of brine geochemistry by fluid mixing or by inputs from Sr and 87 Sr-enriched rock sources. Lithium concentrations are positively correlated with 87 Sr/ 86 Sr ratios and TDS in brines enriched in these constituents. These correlations suggest deeper-seated geogenic sources and have implications for Li exploration in the northern Gulf Coast basin. Normal faults associated with the pre-Jurassic topography may have provided potential pathways for brine migration into the Smackover Formation under the influence of overpressure or thermohaline convection in the Gulf Coast.

Alabama↗

Evaluating drivers of environmental change in a lake sediment core: Insights from spectroscopic metrics of water-extractable organic matter and stable carbon isotopes

Freshwater lakes play a critical role in the global carbon cycle by storing and transforming organic matter (OM) from both terrestrial and aquatic sources. Small lakes in northern temperate regions, despite their limited surface area, disproportionately influence regional carbon budgets. Buried sediments integrate OM inputs over time and archive ecosystem responses to natural and anthropogenic disturbances. However, the direction and magnitude of recent environmental changes on sediment carbon (C) dynamics remain poorly understood. A 23-cm core was collected from a small temperate lake in northeastern USA to evaluate sediment OM content and composition over timescales relevant to historical land-use change, damming, and recovery from acid deposition. Patterns in OM burial and source contributions were revealed via elemental and isotopic analyses of bulk OM and ultraviolet-visible spectrophotometry of water-extractable organic matter (WEOM). The optical metrics expanded observations of likely OM sources beyond the information gained from bulk carbon metrics (total carbon, δ 13 C). The aromaticity of WEOM increased downcore, which is consistent with a shift from increased terrestrial inputs during early logging and damming activity (pre ∼1920) to more microbial-derived OM in recent surficial sediments. Future applications of WEOM optical properties as complements to traditional geochemical metrics can enhance interpretations of lake ecosystem responses recorded in lake sediments to environmental perturbations in temperate lakes.

New York↗

Erosion and transport of sediments in watersheds of southwest Puerto Rico determined from strontium isotopes and mixing models

Sediment outflow from streams to coastal regions can adversely affect water quality and the health of ecosystems including Puerto Rico's southwestern carbonate platform with shallow marine communities. Knowledge of sediment provenance and erosional areas would aid effective restoration to reduce excessive sedimentation. Strontium (Sr) isotopic ratios ( 87 Sr/ 86 Sr) can be used to differentiate between sediment eroded into streams from different lithologies, or rock types, and used in mixing models to estimate proportions of source materials in downstream mixtures. The goal of this study was to use Sr isotopes to differentiate between river sediments in drainages with distinct geologies and present a case study where Sr isotope mixing models are used to identify sediment sourcing to Río Loco and Bahía de Guánica, a priority watershed of the U.S. Coral Reefs Task Force. For the Río Loco watershed, model results indicate that serpentinites in the uplands contributed approximately 71 % of sediment to Bahía de Guánica. About 21 % of sediment was from trachy-andesitic basalts in the foothills, and the remaining 8 % originated from sources on the coastal plain. Neither the uppermost headwater region of Río Loco, the Canal Principal De Riego Valle De Lajas, nor the tributary Quebrada Susúa appeared to be significant sources of sediment to Río Loco's mainstem or Bahía de Guánica at the time of the study. Our results demonstrate that sediment from the serpentinite-bearing areas of Río Loco watershed was effectively transported to the lowlands, which then discharge into Guánica Bay, and highlight the potential use of Sr isotopes as tracers of sediment provenance. This will, in turn, enable better science-based restoration efforts aimed at reducing terrestrial sediment erosion and impacts to marine ecosystems.

Puerto Rico↗