Geology topics

Robert G. Marvinney

Publications and source records attributed to Robert G. Marvinney.

6 recordsLinked to original sources

USGS2023

Implementation plan of the National Cooperative Geologic Mapping Program strategy—Northeast region of the United States: New York and New England

Complexly deformed igneous, metamorphic, and sedimentary rocks form the bedrock of the Northeast region of the United States. Variably thick unconsolidated sediments deposited by glacial, fluvial, and eolian systems locally cover the bedrock. New geologic mapping focuses on areas lacking modern, detailed studies or syntheses, and contributes to existing framework research. This report addresses plans for the continued development of regionally and nationally consistent geologic maps and map databases, efforts to answer outstanding geologic questions, and societal concerns associated with related geologic topics, such as hazards, geologic and hydrologic resources, and environmental issues.

Connecticut, Massachusetts, Maine, New Hampshire, ↗

USGS2023

A recently discovered trachyte-hosted rare earth element-niobium-zirconium occurrence in northern Maine, USA

Reported here are geological, geophysical, mineralogical, and geochemical data on a previously unknown trachyte-hosted rare earth element (REE)-Nb-Zr occurrence at Pennington Mountain in northern Maine, USA. This occurrence was newly discovered by a regional multiparameter, airborne radiometric survey that revealed anomalously high equivalent Th (eTh) and U (eU), confirmed by a detailed ground radiometric survey and by portable X-Ray fluorescence (pXRF) and whole-rock analyses of representative rock samples. The mineralized area occurs within an elongate trachyte body (~1.2 km 2 ) that intrudes Ordovician volcanic rocks. Geologic constraints suggest that the trachyte is also Ordovician in age. The eastern lobe (~900 × ~400 m) of the trachyte is pervasively brecciated with a matrix containing seams, lenses, and veinlets composed mainly of potassium feldspar, albite, and fine-grained zircon and monazite. Barite is locally abundant. Minor minerals within the matrix include columbite, bastnäsite, euxenite, chlorite, pyrite, sphalerite, and magnetite. The pXRF analyses of 22 samples (App. Table A1) collected from the eastern lobe demonstrate that this entire part of the trachyte is highly mineralized. Whole-rock geochemical analyses for samples from the eastern lobe document high average contents of Zr (1.17 wt %), Nb (1,656 ppm), Ba (3,132 ppm), Y (1,140 ppm), Hf (324 ppm), Ta (122 ppm), Th (124 ppm), U (36.5 ppm), Zn (689 ppm), and Sn (106 ppm). Among light REE, the highest average concentrations are shown by La (763 ppm) and Ce (1,479 ppm). For heavy REE (HREE), Dy and Er are the most abundant on average (167 and 114 ppm, respectively). No HREE-rich minerals such as xenotime have been identified; the HREE may reside chiefly in monazite and bastnäsite, and within the fine-grained zircon. Very strong positive correlations (R 2 ) of 0.92 to 0.98 exist between Th and Zr, Nb, Y, Ce, Yb, and Sn, indicating that the radiometric data for eTh are valid proxies for concentrations of these metals in the mineralized rocks.

Maine↗

USGS2022

Potential for critical mineral deposits in Maine, USA

An analysis of the potential for deposits of critical minerals and elements in Maine presented here includes data and discussions for antimony, beryllium, cesium, chromium, cobalt, graphite, lithium, manganese, niobium, platinum group elements, rhenium, rare earth elements, tin, tantalum, tellurium, titanium, uranium, vanadium, tungsten, and zirconium. Deposits are divided into two groups based on geological settings and common ore-deposit terminology. One group consists of known deposits (sediment-hosted manganese, volcanogenic massive sulphide, porphyry copper-molybdenum, mafic- and ultramafic-hosted nickel-copper [-cobalt-platinum group elements], pegmatitic lithium-cesium-tantalum) that are in most cases relatively large, well-documented, and have been explored extensively in the past. The second, and much larger group of different minerals and elements, comprises small deposits, prospects, and occurrences that are minimally explored or unexplored. The qualitative assessment used in this study relies on three key criteria: (1) the presence of known deposits, prospects, or mineral occurrences; (2) favourable geologic settings for having certain deposit types based on current ore deposit models; and (3) geochemical anomalies in rocks or stream sediments, including panned concentrates. Among 20 different deposit types considered herein, a high resource potential is assigned only to three: (1) sediment-hosted manganese, (2) mafic- and ultramafic-hosted nickel-copper(-cobalt-platinum group elements), and (3) pegmatitic lithium-cesium-tantalum. Moderate potential is assigned to 11 other deposit types, including: (1) porphyry copper-molybdenum (-rhenium, selenium, tellurium, bismuth, platinum group elements); (2) chromium in ophiolites; (3) platinum group elements in ophiolitic ultramafic rocks; (4) granite-hosted uranium-thorium; (5) tin in granitic plutons and veins; (6) niobium, tantalum, and rare earth elements in alkaline intrusions; (7) tungsten and bismuth in polymetallic veins; (8) vanadium in black shales; (9) antimony in orogenic veins and replacements; (10) tellurium in epithermal deposits; and (11) uranium in peat.

Maine↗

USGS2014

Uranium and radon in private bedrock well water in Maine: geospatial analysis at two scales

In greater Augusta of central Maine, 53 out of 1093 (4.8%) private bedrock well water samples from 1534 km 2 contained [U] >30 μg/L, the U.S. Environmental Protection Agency’s (EPA) Maximum Contaminant Level (MCL) for drinking water; and 226 out of 786 (29%) samples from 1135 km 2 showed [Rn] >4,000 pCi/L (148 Bq/L), the U.S. EPA’s Alternative MCL. Groundwater pH, calcite dissolution and redox condition are factors controlling the distribution of groundwater U but not Rn due to their divergent chemical and hydrological properties. Groundwater U is associated with incompatible elements (S, As, Mo, F, and Cs) in water samples within granitic intrusions. Elevated [U] and [Rn] are located within 5–10 km distance of granitic intrusions but do not show correlations with metamorphism at intermediate scales (100−101 km). This spatial association is confirmed by a high-density sampling (n = 331, 5–40 samples per km 2 ) at local scales (≤10 –1 km) and the statewide sampling (n = 5857, 1 sample per 16 km 2 ) at regional scales (10 2 –10 3 km). Wells located within 5 km of granitic intrusions are at risk of containing high levels of [U] and [Rn]. Approximately 48 800–63 900 and 324 000 people in Maine are estimated at risk of exposure to U (>30 μg/L) and Rn (>4000 pCi/L) in well water, respectively.

Maine↗

USGS2014

Flow and sorption controls of groundwater arsenic in individual boreholes from bedrock aquifers in central Maine, USA

To understand the hydrogeochemical processes regulating well water arsenic (As) evolution in fractured bedrock aquifers, three domestic wells with [As] up to 478 μg/L are investigated in central Maine. Geophysical logging reveals that fractures near the borehole bottom contribute 70-100% of flow. Borehole and fracture water samples from various depths show significant proportions of As (up to 69%) and Fe (93-99%) in particulates (>0.45 μm). These particulates and those settled after a 16-day batch experiment contain 560-13,000 g/kg of As and 14-35% weight/weight of Fe. As/Fe ratios (2.5-20 mmol/mol) and As partitioning ratios (adsorbed/dissolved [As], 20,000-100,000 L/kg) suggest that As is sorbed onto amorphous hydrous ferric oxides. Newly drilled cores also show enrichment of As (up to 1300 mg/kg) sorbed onto secondary iron minerals on the fracture surfaces. Pumping at high flow rates induces large decreases in particulate As and Fe, a moderate increase in dissolved [As] and As(III)/As ratio, while little change in major ion chemistry. The δD and δ 18 O are similar for the borehole and fracture waters, suggesting a same source of recharge from atmospheric precipitation. Results support a conceptual model invoking flow and sorption controls on groundwater [As] in fractured bedrock aquifers whereby oxygen infiltration promotes the oxidation of As-bearing sulfides at shallower depths in the oxic portion of the flow path releasing As and Fe; followed by Fe oxidation to form Fe oxyhydroxide particulates, which are transported in fractures and sorb As along the flow path until intercepted by boreholes. In the anoxic portions of the flow path, reductive dissolution of As-sorbed iron particulates could re-mobilize As. For exposure assessment, we recommend sampling of groundwater without filtration to obtain total As concentration in groundwater.

Maine↗

USGS2012

Can arsenic occurrence rate in bedrock aquifers be predicted?

A high percentage (31%) of groundwater samples from bedrock aquifers in the greater Augusta area, Maine was found to contain greater than 10 μg L –1 of arsenic. Elevated arsenic concentrations are associated with bedrock geology, and more frequently observed in samples with high pH, low dissolved oxygen, and low nitrate. These associations were quantitatively compared by statistical analysis. Stepwise logistic regression models using bedrock geology and/or water chemistry parameters are developed and tested with external data sets to explore the feasibility of predicting groundwater arsenic occurrence rates (the percentages of arsenic concentrations higher than 10 μg L –1 ) in bedrock aquifers. Despite the under-prediction of high arsenic occurrence rates, models including groundwater geochemistry parameters predict arsenic occurrence rates better than those with bedrock geology only. Such simple models with very few parameters can be applied to obtain a preliminary arsenic risk assessment in bedrock aquifers at local to intermediate scales at other localities with similar geology.

Environmental Science & Technology↗