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USGS2017

Soils as relative-age dating tools

Soils develop at the earth's surface via multiple processes that act through time. Precluding burial or disturbance, soil genetic horizons form progressively and reflect the balance among formation processes, surface age, and original substrate composition. Soil morphology provides a key link between process and time (soil age), enabling soils to serve as both relative and numerical dating tools for geomorphic studies and landscape evolution. Five major factors define the contemporary state of all soils: climate, organisms, topography, parent material, and time. Soils developed on similar landforms and parent materials within a given landscape comprise what we term a soil/landform/substrate complex. Soils on such complexes that differ in development as a function of time represent a soil chronosequence. In a soil chronosequence, time constitutes the only independent formation factor; the other factors act through time. Time dictates the variations in soil development or properties (field or laboratory measured) on a soil/landform/substrate complex. Using a dataset within the chronosequence model, we can also formulate various soil development indices based upon one or a combination of soil properties, either for individual soil horizons or for an entire profile. When we evaluate soil data or soil indices mathematically, the resulting equation creates a chronofunction. Chronofunctions help quantify processes and mechanisms involved in soil development, and relate them mathematically to time. These rigorous kinds of comparisons among and within soil/landform complexes constitute an important tool for relative-age dating. After determining one or more absolute ages for a soil/landform complex, we can calculate quantitative soil formation, and or landform-development rates. Multiple dates for several complexes allow rate calculations for soil/landform-chronosequence development and soil-chronofunction calibration.

Book chapter↗

USGS1990

Adsorption of selenium by amorphous iron oxyhydroxide and manganese dioxide

This work compares and models the adsorption of selenium and other anions on a neutral to alkaline surface (amorphous iron oxyhydroxide) and an acidic surface (manganese dioxide). Selenium adsorption on these oxides is examined as a function of pH, particle concentration, oxidation state, and competing anion concentration in order to assess how these factors might influence the mobility of selenium in the environment. The data indicate that 1. 1) amorphous iron oxyhydroxide has a greater affinity for selenium than manganese dioxide, 2. 2) selenite [Se(IV)] adsorption increases with decreasing pH and increasing particle concentration and is stronger than selenate [Se(VI)] adsorption on both oxides, and 3. 3) selenate does not adsorb on manganese dioxide. The relative affinity of selenate and selenite for the oxides and the lack of adsorption of selenate on a strongly acidic surface suggests that selenate forms outer-sphere complexes while selenite forms inner-sphere complexes with the surfaces. The data also indicate that the competition sequence of other anions with respect to selenite adsorption at pH 7.0 is phosphate > silicate > molybdate > fluoride > sulfate on amorphous iron oxyhydroxide and molybdate ??? phosphate > silicate > fluoride > sulfate on manganese dioxide. The adsorption of phosphate, molybdate, and silicate on these oxides as a function of pH indicates that the competition sequences reflect the relative affinities of these anions for the surfaces. The Triple Layer surface complexation model is used to provide a quantitative description of these observations and to assess the importance of surface site heterogeneity on anion adsorption. The modeling results suggest that selenite forms binuclear, innersphere complexes with amorphous iron oxyhydroxide and monodentate, inner-sphere complexes with manganese dioxide and that selenate forms outer-sphere, monodentate complexes with amorphous iron oxyhydroxide. The heterogeneity of the oxide surface sites is reflected in decreasing equilibrium constants for selenite with increasing adsorption density and both experimental observations and modeling results suggest that manganese dioxide has fewer sites of higher energy for selenite adsorption than amorphous iron oxyhydroxide. Modeling and interpreting the adsorption of phosphate, molybdate, and silicate on the oxides are made difficult by the lack of constraint in choosing surface species and the fact that equally good fits can be obtained with different surface species. Finally, predictions of anion competition using the model results from single adsorbate systems are not very successful because the model does not account for surface site heterogeneity. Selenite adsorption data from a multi-adsorbate system could be fit if the equilibrium constant for selenite is decreased with increasing anion adsorption density.

Geochimica et Cosmochimica Acta↗

USGS2008

Dissolved metals and associated constituents in abandoned coal-mine discharges, Pennsylvania, USA. Part 2: Geochemical controls on constituent concentrations

Water-quality data for discharges from 140 abandoned mines in the Anthracite and Bituminous Coalfields of Pennsylvania reveal complex relations among the pH and dissolved solute concentrations that can be explained with geochemical equilibrium models. Observed values of pH ranged from 2.7 to 7.3 in the coal-mine discharges (CMD). Generally, flow rates were smaller and solute concentrations were greater for low-pH CMD samples; pH typically increased with flow rate. Although the frequency distribution of pH was similar for the anthracite and bituminous discharges, the bituminous discharges had smaller median flow rates; greater concentrations of SO4, Fe, Al, As, Cd, Cu, Ni and Sr; comparable concentrations of Mn, Cd, Zn and Se; and smaller concentrations of Ba and Pb than anthracite discharges with the same pH values. The observed relations between the pH and constituent concentrations can be attributed to (1) dilution of acidic water by near-neutral or alkaline ground water; (2) solubility control of Al, Fe, Mn, Ba and Sr by hydroxide, sulfate, and/or carbonate minerals; and (3) aqueous SO4-complexation and surface-complexation (adsorption) reactions. The formation of AlSO4+ and AlHSO42 + complexes adds to the total dissolved Al concentration at equilibrium with Al(OH)3 and/or Al hydroxysulfate phases and can account for 10-20 times greater concentrations of dissolved Al in SO4-laden bituminous discharges compared to anthracite discharges at pH of 5. Sulfate complexation can also account for 10-30 times greater concentrations of dissolved FeIII concentrations at equilibrium with Fe(OH)3 and/or schwertmannite (Fe8O8(OH)4.5(SO4)1.75) at pH of 3-5. In contrast, lower Ba concentrations in bituminous discharges indicate that elevated SO4 concentrations in these CMD sources could limit Ba concentrations by the precipitation of barite (BaSO4). Coprecipitation of Sr with barite could limit concentrations of this element. However, concentrations of dissolved Pb, Cu, Cd, Zn, and most other trace cations in CMD samples were orders of magnitude less than equilibrium with sulfate, carbonate, and/or hydroxide minerals. Surface complexation (adsorption) by hydrous ferric oxides (HFO) could account for the decreased concentrations of these divalent cations with increased pH. In contrast, increased concentrations of As and, to a lesser extent, Se with increased pH could result from the adsorption of these oxyanions by HFO at low pH and desorption at near-neutral pH. Hence, the solute concentrations in CMD and the purity of associated "ochres" formed in CMD settings are expected to vary with pH and aqueous SO4 concentration, with potential for elevated SO4, As and Se in ochres formed at low pH and elevated Cu, Cd, Pb and Zn in ochres formed at near-neutral pH. Elevated SO4 content of ochres could enhance the adsorption of cations at low pH, but decrease the adsorption of anions such as As. Such information on environmental processes that control element concentrations in aqueous samples and associated precipitates could be useful in the design of systems to reduce dissolved contaminant concentrations and/or to recover potentially valuable constituents in mine effluents.

Applied Geochemistry↗

USGS2018

A sequential selective dissolution method to quantify storage and stability of organic carbon associated with Al and Fe hydroxide phases

Stabilization of SOM (soil organic matter) is regulated in part by sorption and desorption reactions happening at mineral surfaces, as well as precipitation and dissolution of organo-metal complexes. Fe and Al hydroxides play a particularly significant role in SOM stabilization in soils due to their ubiquitous distribution and their highly reactive surface properties. Iron and Al hydroxides exist in soils across a wide spectrum of crystallinity, ranging from dissolved Fe and Al cations which combine with organics to form organo-metal precipitates to the more crystalline end members, goethite and gibbsite, which sorb SOM through a variety of molecular interactions. Though the importance of these sorption and precipitation reactions has long been recognized, the distribution of SOM among Fe and Al hydroxides of differing crystallinity has not been well quantified, nor has the timescale over which these stabilization mechanisms operate. In an attempt to measure the distribution of organic C among (i) Al- and Fe-humus complexes (ii) short-range-order (SRO) Al and Fe hydroxide surfaces and (iii) crystalline Fe oxyhydroxide surfaces, a single method combining several selective mineral dissolutions was applied to soils of four different geneses (a tropical forest Andisol, a temperate forest basaltic Mollisol, a Mediterranean coastal prairie Mollisol, and a northern mixed hardwood forest Spodosol). The traditional reactants used in selective dissolutions were replaced with carbon-free analogues so that the carbon released along with the Fe and Al at each stage of the selective dissolution process could be measured. Selective dissolutions were performed sequentially: Na-pyrophosphate (organo-Al and Fe complexes) followed by hydroxylamine (SRO Al and Fe hydroxides) followed by dithionite-HCl (crystalline Fe hydroxides). Carbon, Al, and Fe concentrations, as well as radiocarbon abundance were measured in the solutions yielded by each stage of the selective dissolution process. Results suggest that precipitation of organo-metal complexes (Na-pyrophosphate extractable C) often accounts for the largest pool of stabilized C among the three selectively dissolved pools, but these complexes were 14 C enriched in comparison to C from the other selectively dissolved pools and the residual C left on crystalline mineral surfaces after all three stages of selective dissolution. Hydroxylamine and dithionite-HCl extractable C pools were, on average, small and often below detection level in temperate soils. However, radiocarbon values for these C pools were generally depleted in comparison to other pools. These results suggest variation in organo-mineral complex stability is associated with degree of crystallinity of the mineral phase. Overall, this work suggests that sequential selective dissolution methods are a promising tool for characterizing the content and isotopic composition of soil C associated with distinct organo-mineral and organo-metal associations.

Geoderma↗

USGS2002

Molecular structure of the decamolybdodicobaltate(III) ion

When solutions of cobalt(II) ion and heptamolybdate ion (Mo₇O₂₄⁶⁻) are mixed in the presence of an oxidizing agent (such as bromine), Kurnakov, Hall, and others found that an emerald green complex is formed as the main product, namely, the heteropoly complex ion hexamolybdocobaltate(III), which forms salts such as (NH₄)₃[H₆CoMo₆O₂₄]·12H₂O. Friedheim and Keller showed that at the same time a small amount of another complex is also formed, having a Co:Mo ratio of 1:5. Tsigdinos, et al., found that if a hot solution of the hexamolybdocobaltate complex ion is treated with activated charcoal or Raney nickel the 1:6 complex is converted almost entirely to the 1:5 complex. These workers proved the latter to be a dimer, and formulated the ammonium salt (earlier prepared by Friedheim and Keller) as (NH₄)₆[Co₂Mo₁₀O₃₆]·10H₂O. We have now completed a crystal structure analysis of this interesting compound, which shows the proper formula to be (NH₄)₆[H₄Co₃Mo₁₀O₃₈]·7H₂O.

Journal of the American Chemical Society↗

USGS1996

Experimental investigation and modeling of uranium (VI) transport under variable chemical conditions

The transport of adsorbing and complexing metal ions in porous media was investigated with a series of batch and column experiments and with reactive solute transport modeling. Pulses of solutions containing U(VI) were pumped through columns filled with quartz grains, and the breakthrough of U(VI) was studied as a function of variable solution composition ( p H, total U(VI) concentration, total fluoride concentration, and p H-buffering capacity). Decreasing p H and the formation of nonadsorbing aqueous complexes with fluoride increased U(VI) mobility. A transport simulation with surface complexation model (SCM) parameters estimated from batch experiments was able to predict U(VI) retardation in the column experiments within 30%. SCM parameters were also estimated directly from transport data, using the results of three column experiments collected at different p H and U(VI) pulse concentrations. SCM formulations of varying complexity (multiple surface types and reaction stoichiometries) were tested to examine the trade-off between model simplicity and goodness of fit to breakthrough. A two-site model (weak- and strong-binding sites) with three surface complexation reactions fit these transport data well. With this reaction set the model was able to predict (1) the effects of fluoride complexation on U(VI) retardation at two different p H values and (2) the effects of temporal variability of p H on U(VI) transport caused by low p H buffering. The results illustrate the utility of the SCM approach in modeling the transport of adsorbing inorganic solutes under variable chemical conditions.

Water Resources Research↗

USGS1945

Petrography, structures, and petrofabrics of the Pinckneyville quartz diorite, Alabama

The Pinckneyville quartz diorite complex underlies an area in eastern Alabama extending from the Coosa River in northwest Elmore County northeast through Coosa and Tallapoosa counties into Clay County. Dark-gray, coarse-grained quartz diorite gneiss constitutes the major part of the complex, but there are smaller amounts of granodiorite and granite gneiss. Hornblende-biotite gneisses also occur and are considered to represent metamorphosed basic sills and dikes intruded before the quartz diorite complex. Schist septa lie within the complex and are usually parallel to the regional strike. The sequence of intrusion as interpreted from inclusions and petrographic data is (1) quartz diorite, (2) granodiorite, (3) granite. Small but persistent amounts of allanite and epidote are characteristic of the rocks of the complex. The texture is subporphyritic and shows evidence of protoclastic deformation. A northeast-southwest trend of inclusions, foliation, lineation, and contacts dominates. Primary flow structures are shown in the orientation of inclusions and micas. Secondary structures were superposed on the original flow structures shortly after intrusion and prior to complete consolidation. A prominent secondary structure is a lineation in b. Stretching in b is indicated by boudinage structures, the lineation, and small displacements of dikes. The intensity of the planar structures in the gneiss grades from strong to indistinct or lacking from east to west. Structures in schist inclusions indicate that some folding had taken place prior to intrusion. Thin pegmatite, granodiorite, and granite dikes are common. Most of them are essentially parallel to the regional strike. The petrographic boundary between gneiss and schist is always sharp. On a large scale, the gneiss structures are essentially parallel to the contacts, but slight to marked discordant relations occur at many localities. The schist structures usually parallel the contacts. Petrofabric analysis confirms the structural field observations. The mica fabrics are ac -girdles and are most complete where the foliation is weakest. Microscopic s -planes do not always coincide with the observed foliation. The quartz fabrics are also ac -girdles but are not so well developed as the mica girdles. Quartz orientations cannot always be related to known s -planes. It is concluded that the Pinckneyville quartz diorite complex represents a syntectonic intrusion—that is, that intrusion took place while external or regional forces were still active. The shape of the intrusion was controlled largely by the wall-rock structures which had developed earlier. The rocks show both igneous and metamorphic characteristics because the intrusion took place under regional metamorphic conditions.

Alabama↗

USGS2020

An analysis of the factors that control fault zone architecture and the importance of fault orientation relative to regional stress

The moment magnitude 7.2 El Mayor−Cucapah (EMC) earthquake of 2010 in northern Baja California, Mexico produced a cascading rupture that propagated through a geometrically diverse network of intersecting faults. These faults have been exhumed from depths of 6−10 km since the late Miocene based on low-temperature thermochronology, synkinematic alteration, and deformational fabrics. Coseismic slip of 1−6 m of the EMC event was accommodated by fault zones that displayed the full spectrum of architectural styles, from simple narrow fault zones (<100 m in width) that have a single high-strain core, to complex wide fault zones (>100 m in width) that have multiple anastomosing high-strain cores. As fault zone complexity and width increase the full spectrum of observed widths (20−200 m), coseismic slip becomes more broadly distributed on a greater number of scarps that form wider arrays. Thus, the infinitesimal slip of the surface rupture of a single earthquake strongly replicates many of the fabric elements that were developed during the long-term history of slip on the faults at deeper levels of the seismogenic crust. We find that factors such as protolith, normal stress, and displacement, which control gouge production in laboratory experiments, also affect the architectural complexity of natural faults. Fault zones developed in phyllosilicate-rich metasedimentary gneiss are generally wider and more complex than those developed in quartzo-feldspathic granitoid rocks. We hypothesize that the overall weakness and low strength contrast of faults developed in phyllosilicate rich host rocks leads to strain hardening and formation of broad, multi-stranded fault zones. Fault orientation also strongly affects fault zone complexity, which we find to increase with decreasing fault dip. We attribute this to the higher resolved normal stresses on gently dipping faults assuming a uniform stress field compatible with this extensional tectonic setting. The conditions that permit slip on misoriented surfaces with high normal stress should also produce failure of more optimally oriented slip systems in the fault zone, promoting complex branching and development of multiple high-strain cores. Overall, we find that fault zone architecture need not be strongly affected by differences in the amount of cumulative slip and instead is more strongly controlled by protolith and relative normal stress.

Baja California↗

USGS1989

Tectonostratigraphic terranes and their Paleozoic boundaries in the central and southern Appalachians

Parts of the central and southern Appalachian orogen appear to have evolved away from Proterozoic North America (Laurentia) and to have been accreted to it during the Paleozoic orogenies that collectively formed the orogen. Identifying each tectonostratigraphic terrane is a necessary step in understanding the evolution of the orogen. The terranes in the central and southern Appalachians are delineated, interpreted, and classified with varying degrees of confidence as: (1) Laurentian native terranes , (2) internal continental terranes of the Appalachian orogen, (3) disrupted terranes , (4) possible oceanic crustal remnants, (5) volcanic-arc terranes , (6) a continental terrane of Gondwanaland affinity, and (7) metamorphic complexes of undetermined affinity. The Laurentian native terranes consist of external massifs of Laurentian basement (Grenvillian and older), their rift- and shelf-facies cover rocks, and slope-rise prism deposits. External massifs are present in the Blue Ridge tectonic province, Reading Prong, and Honey Brook Upland. Rocks of the Talladega block are stratigraphically tied to Laurentia and, with the possible exception of the Hillabee greenstone, are also considered native. Offshore, deep-water, post-rift deposits of the Hamburg and Westminster terranes have no direct stratigraphic ties to Laurentia and are considered discrete native (not suspect) terranes . The internal continental terranes of the Appalachian orogen are isolated massifs of Middle Proterozoic (Grenvillian) continental basement and their cover sequences that occur within the metamorphic core of the orogen. These terranes , the Baltimore, Sauratown, and Pine Mountain terranes , could be either structurally isolated outliers of Laurentia or microcontinental fragments of Laurentian crust displaced by rifting or transcurrent faulting and later reassembled. Disrupted terranes in the central and southern Appalachians contain mélange complexes as well as more coherent terrane fragments (volcanic, ophiolitic, or continental) intermingled with the mélange complexes. Those identified include the Jefferson, Potomac, Smith River, Inner Piedmont, Falls Lake, Juliette, and Sussex terranes . The Bel Air-Rising Sun terrane (Baltimore Complex) in Maryland and Pennsylvania is the only terrane named separately as a possible oceanic crustal remnant. Similar mafic and ultramafic complexes are present in all of the disrupted terranes , but are too small to consider as separate terranes . Volcanic-arc terranes include the Chopawamsic, Carolina, Spring Hope, Roanoke Rapids, and Charleston terranes . The only terrane recognized as a continental terrane of Gondwanaland affinity is the Suwannee terrane , which contains rocks believed to correlate with those now exposed in west Africa. Metamorphic complexes of undetermined affinity are terranes that could not be clearly classified on the basis of available data. These include the Milton, Gaffney, Uchee, Crabtree, Goochland, Wilmington, and Hatteras terranes . The Penobscottian, Taconian, Acadian, and Alleghanian Paleozoic compressional events collectively assembled the various terranes into what is now the Appalachian orogen. Only the central and southern parts of the U.S. Appalachians are considered here. The Penobscottian orogeny, about 550 to 490 Ma, amalgamated the Potomac, the Chopawamsic, probably the Bel Air-Rising Sun, and possibly other exotic terranes at some unknown distance from Laurentia. This was followed by the Taconian orogeny, about 470 to 440 Ma, which accreted the previously amalgamated terranes and probably other terranes such as the Carolina terrane to Laurentia. The younger age limit for the Taconian event is partly constrained by Middle and Late Ordovician faunal assemblages in successor basin deposits of the Arvonia Slate and Quantico Formation. The significance of the Acadian orogeny, dated about 400 to 380 Ma in New England, is unclear in the central and southern Appalachians . In the Talladega block of Alabama and Georgia, an Early to Middle Devonian dynamothermal event is firmly bracketed between Early Devonian fossils and K-Ar ages that indicate a thermal peak no later than Middle Devonian time. A regional tectonothermal event and faulting of approximately this age are also suggested by isotopic studies in terranes to the east. The late Paleozoic (Alleghanian) continental collision between Laurentia and Gondwanaland, which formed the supercontinent Pangea, marks the final stage of accretionary history in the Appalachian -Caledonide orogen. Effects evident in the central and southern Appalachian region include: (1) the accretion of the Suwannee terrane and perhaps the Charleston terrane to what is now North America, (2) slicing and shifting of terranes along dextral strike-slip faults, particularly in the eastern Piedmont, (3) westward transport of native and previously accreted terranes in the western Piedmont and Blue Ridge as part of a composite crystalline thrust sheet, (4) deposition of clastic wedges in the Appalachian foreland, and (5) imbricate thrusting and folding of the resultant strata in the Valley and Ridge Province.

Appalachians↗

USGS1999

Lead isotope compositions of Late Cretaceous and early Tertiary igneous rocks and sulfide minerals in Arizona: Implications for the sources of plutons and metals in porphyry copper deposits

Porphyry copper deposits in Arizona are genetically associated with Late Cretaceous and early Tertiary igneous complexes that consist of older intermediate volcanic rocks and younger intermediate to felsic intrusions. The igneous complexes and their associated porphyry copper deposits were emplaced into an Early Proterozoic basement characterized by different rocks, geologic histories, and isotopic compositions. Lead isotope compositions of the Proterozoic basement rocks define, from northwest to southeast, the Mojave, central Arizona, and southeastern Arizona provinces. Porphyry copper deposits are present in each Pb isotope province. Lead isotope compositions of Late Cretaceous and early Tertiary plutons, together with those of sulfide minerals in porphyry copper deposits and of Proterozoic country rocks, place important constraints on genesis of the magmatic suites and the porphyry copper deposits themselves. The range of age-corrected Pb isotope compositions of plutons in 12 Late Cretaceous and early Tertiary igneous complexes is 206 Pb/ 204 Pb = 17.34 to 22.66, 207 Pb/ 204 Pb = 15.43 to 15.96, and 208 Pb/ 204 Pb = 37.19 to 40.33. These Pb isotope compositions and calculated model Th/U are similar to those of the Proterozoic rocks in which the plutons were emplaced, thereby indicating that Pb in the younger rocks and ore deposits was inherited from the basement rocks and their sources. No Pb isotope differences distinguish Late Cretaceous and early Tertiary igneous complexes that contain large economic porphyry copper deposits from less rich or smaller deposits that have not been considered economic for mining. Lead isotope compositions of Late Cretaceous and early Tertiary plutons and sulfide minerals from 30 metallic mineral districts, furthermore, require that the southeastern Arizona Pb province be divided into two subprovinces. The northern subprovince has generally lower 206 Pb/ 204 Pb and higher model Th/U, and the southern subprovince has higher 206 Pb/ 204 Pb and lower model Th/U. These Pb isotope differences are inferred to result from differences in their respective post-1.7 Ga magmatic histories. Throughout Arizona, Pb isotope compositions of Late Cretaceous and early Tertiary plutons and associated sulfide minerals are distinct from those of Jurassic plutons and also middle Tertiary igneous rocks and sulfide minerals. These differences most likely reflect changes in tectonic setting and magmatic sources. Within Late Cretaceous and early Tertiary igneous complexes that host economic porphyry copper deposits, there is commonly a decrease in Pb isotope composition from older to younger plutons. This decrease in Pb isotope values with time suggests an increasing involvement of crust with lower U/Pb than average crust in the source(s) of Late Cretaceous and early Tertiary magmas. Lead isotope compositions of the youngest porphyries in the igneous complexes are similar to those in most sulfide minerals within the associated porphyry copper deposit. This Pb isotope similarity argues for a genetic link between them. However, not all Pb in the sulfide minerals in porphyry copper deposits is magmatically derived. Some sulfide minerals, particularly those that are late stage, or distal to the main orebody, or in Proterozoic or Paleozoic rocks, have elevated Pb isotope compositions displaced toward the gross average Pb isotope composition of the local country rocks. The more radiogenic isotopic compositions argue for a contribution of Pb from those rocks at the site of ore deposition. Combining the Pb isotope data with available geochemical, isotopic, and petrologic data suggests derivation of the young porphyry copper-related plutons, most of their Pb, and other metals from a hybridized lower continental crustal source. Because of the likely involvement of subduction-related mantle-derived basaltic magma in the hybridized lower crustal source, an indiscernible mantle contribution is probable in the porphyry magmas. Clearly, in addition, Pb was contributed from the local country rocks. This is most evident in sulfide minerals in veins that are late stage, hosted in Proterozoic gneiss, and/or peripheral to the porphyry copper deposit.

Economic Geology↗

USGS2003

Geologic map of the Bonners Ferry 30' x 60' quadrangle, Idaho and Montana

This data set maps and describes the geology of the Bonners Ferry 30' x 60' quadrangle, Idaho and Montana. The bedrock geology of the Bonners Ferry quadrangle consists of sedimentary, metamorphic, and granitic rocks ranging in age from Middle Proterozoic to Eocene. Bedrock units include rocks of (1) the Middle Proterozoic Belt Supergroup (2) the Middle Proterozoic Deer Trail Group, (3) the Late Proterozoic Windermere Group, (4) miogeoclinal or shelf facies lower Paleozoic rocks, and (5) Mesozoic and Tertiary granitic rocks. The Belt Supergroup, a thick sequence of argillite, siltite, quartzite, and impure carbonate rocks up to 9,000 m thick, occurs in two non-contiguous sequences in the quadrangle: (1) the Clark Fork-Eastport Sequence east of the Purcell trench and (2) the Newport Sequence in the hanging wall of the Newport Fault. Only the two lowest Belt formations of the Newport Sequence are found in the Bonners Ferry quadrangle, but these two units are part of a continuous section, which extends southwestward to the town of Newport. Belt Supergroup rocks of the Clark Fork-Eastport Sequence are separated from those of the Newport Sequence by the Newport Fault, Priest River Complex, and Purcell Trench Fault. Some formations of the Belt Supergroup show differences in thickness and (or) lithofacies from one sequence to the other that are greater than those predicted from an empirical depositional model for the distances currently separating the sequences. These anomalous thickness and facies differences suggest that there has been a net contraction along structures separating the sequences despite Eocene extension associated with emplacement of the Priest River Complex. In addition to these two Belt sequences, probable Belt rocks are present in the Priest River Complex as high metamorphic grade crystalline schist and gneiss. Northwest of the Newport Sequence of Belt Supergroup is the Deer Trail Group, a distinct Middle Proterozoic sequence of argillite, siltite, quartzite, and carbonate rocks lithostratigraphically similar to the Belt Supergroup, but separated from all Belt Supergroup rocks by the Jumpoff Joe Fault. Rocks of the Deer Trail Group are pervasively phyllitic and noticeably more deformed than rocks in the Belt Supergroup sequences. Lithostratigraphically the Deer Trail Group is equivalent to part of the upper part of the Belt Supergroup. Differences in lithostratigraphy and thickness between individual Deer Trail and Belt units and between the Deer Trail and Belt sequences as a whole indicate that they were probably much farther apart when they were deposited. The Windermere Group is a lithologically varied sequence of volcanic rocks and coarse-grained, mostly immature, clastic sedimentary rocks up to 8,000 m thick. It is characterized by extreme differences in thickness and lithofacies over short distances caused by syndepositional faulting associated with initial stages of continental rifting in the Late Proterozoic. Strata of the Windermere Group unconformably overlie only the Deer Trail Group, and are nowhere found in depositional contact with Belt Supergroup rocks. Paleozoic rocks in the Bonners Ferry quadrangle consist of a thin, fault-bounded remnant preserved within the Clark Fork-Eastport Belt Supergroup Sequence. Mesozoic granitic rocks underlie at least 50 percent of the Bonners Ferry quadrangle. They fall into two petrogenetic suites, hornblende-biotite plutons and muscovite-biotite (two-mica) plutons, most of which are Cretaceous in age. Both suites are represented in the mid-crustal Priest River Complex and in the higher level plutons that flank the complex; by far the majority of the Priest River Complex are Cretaceous, two-mica bodies. Tertiary rocks are restricted to a single small stock, numerous hypabyssal dikes that are too small to show at the scale of the map, and to cataclastic rocks related to the Newport Fault. Quaternary deposits include unconsolidated to poorl

Miscellaneous Field Studies Map↗

USGS2003

Regional sediment budget of the Columbia River littoral cell, USA: Analysis of bathymetric- and topographic-volume change

In this Open-File Report we present calculations of changes in bathymetric and topographic volumes for the Grays Harbor, Willapa Bay, and Columbia River entrances and the adjacent coasts of North Beach, Grayland Plains, Long Beach, and Clatsop Plains for four intervals: pre-jetty - 1920s (Interval 1), 1920s - 1950s (Interval 2), 1950s - 1990s (Interval 3), and 1920s 1990s (Interval 4). This analysis is part of the Southwest Washington Coastal Erosion Study (SWCES), the goals of which are to understand and predict the morphologic behavior of the Columbia River littoral cell on a management scale of tens of kilometers and decades. We obtain topographic Light Detection and Ranging (LIDAR) data from a joint project by the U.S. Geological Survey (USGS), National Oceanic and Atmospheric Administration (NOAA), National Aeronautic and Space Administration (NASA), and the Washington State Department of Ecology (DOE) and bathymetric data from the U.S. Coast and Geodetic Survey (USC&GS), U.S. Army Corps of Engineers (USACE), USGS, and the DOE. Shoreline data are digitized from T-Sheets and aerial photographs from the USC&GS and National Ocean Service (NOS). Instead of uncritically adjusting each survey to NAVD88, a common vertical land-based datum, we adjust some surveys to produce optimal results according to the following criteria. First, we minimize offsets in overlapping surveys within the same era, and second, we minimize bathymetric changes (relative to the 1990s) in deep water, where we assume minimal change has taken place. We grid bathymetric and topographic datasets using kriging and triangulation algorithms, calculate bathymetric-change surfaces for each interval, and calculate volume changes within polygons that are overlaid on the bathymetric-change surfaces. We find similar morphologic changes near the entrances to Grays Harbor and the Columbia River following jetty construction between 1898 and 1916 at the Grays Harbor entrance and between 1885 and 1913 at the Columbia River entrance. The inlets and inner deltas eroded and the outer deltas moved offshore and accreted. The adjacent coasts experienced accretion over alongshore distances of tens of kilometers. North of the Grays Harbor entrance along North Beach and north of the Columbia River entrance along Long Beach the shoreface and the beach-dune complex mainly prograded, whereas south of the Grays Harbor entrance along Grayland Plains and south of the Columbia River entrance along Clatsop Plains the beach-dune complex above -10 m NAVD88 prograded and the shoreface between approximately -30 m and -10 m NAVD88 eroded. In the decades following jetty construction, the rates of erosion and accretion at the entrances decreased and the centers of deposition along the adjacent coasts moved away from the entrances. The rates of change have decreased, suggesting the systems are approaching dynamic equilibrium. Exceptions to this behaviour are the accretion of the beach-dune complex of Long Beach, the erosion of Cape Shoalwater, and the northward migration of the Willapa Bay ebb-tidal delta during all intervals. The net shoreline advance of Long Beach increases from 0.28 m/yr in pre-jetty conditions to 3.78 m/yr during Interval 4. The erosion of Cape Shoalwater and the northward migration of the Willapa Bay ebb-tidal delta are related to the northern migration of the Willapa Bay North Channel. Volume changes at the Grays Harbor, Willapa Bay, and Columbia River entrances and the Columbia River estuary are balanced against losses and gains due to littoral transport and sand supply from the Columbia River. Based on these sediment balances, we infer the following pathways: sand that eroded from the inlets and inner deltas at the Grays Harbor and Columbia River entrances moved offshore and northward to accrete the outer deltas and the beaches to the north; sand from the south flank of the Grays Harbor delta and shelf along Grayland Plains moved onshore to accrete the beach dune complex of Grayland Plains and moved northward to maintain accretion of the outer delta and the beach-dune complex of North Beach; sand that eroded from the south flank of the Columbia River delta and shelf along Clatsop Plains contributed to the accretion of the beach-dune complex of Clatsop Plains and the Columbia River outer delta. The net volume change for Interval 1 and 3 at the Grays Harbor entrance and for Interval 1 at the Columbia River entrance is erosion, whereas the net change for the other intervals is accretion. For the entire CRLC, there is a net loss of 185 Mm 3 for Interval 1, a net gain of 357 Mm 3 for Interval 2, and a net gain of 187 Mm 3 for Interval 3. These imbalances can be the result of incomplete bathymetric coverage of the bays and shoreface, uncertainties in the adjustments of vertical tidal datums, inconsistencies in the bathymetric data, and uncertainties in the sediment supply of the Columbia River.

Oregon, Washington↗

USGS2015

Mineral potential for nickel, copper, platinum group elements(PGE), and chromium deposits hosted in ultramafic rocks in the Islamic Republic of Mauritania (phase V, deliverable 67)

PRISM-I summary documents mention the presence of mafic-ultramafic igneous intrusive rocks in several areas of Mauritania and a number of chromium (Cr) and copper-nickel (Cu-Ni (±Co, Au)) occurrences associated with them. Permissive geologic settings generally include greenstone belts of any age, layered mafic-ultramafic and unlayered gabbro-anorthosite intrusive complexes in cratonic settings, ophiolite complexes, flood basalt provinces, and fluid-rich shear zones cutting accumulations of mafic-ultramafic rocks. Regions of Mauritania having these characteristics that are discussed in PRISM-I texts include the Mesoarchean greenstone belts of the TasiastTijirit terrane in the southwestern Rgueïbat Shield, two separate layered ultramafic complexes in the Amsaga Complex west of Atar, serpentinized metadunites in Mesoarchean rocks of the Rgueïbat Shield in the Zednes map sheet, several lateritized annular mafic-ultramafic complexes in the Paleoproterozoic northwestern portion of the Rgueïbat Shield, and the serpentinized ophiolitic segments of the Gorgol Noir Complex in the axial portion of the southern Mauritanides. Bureau de Recherches Géologiques et Minières (BRGM) work in the “Extreme Sud” zone also suggests that small copper occurrences associated with the extensive Jurassic microgabbroic intrusive rocks in the Taoudeni Basin of southeastern Mauritania could have potential for magmatic Cu-Ni (PGE, Co, Au) sulfide mineralization. Similarly, Jurassic mafic intrusive rocks in the northeastern Taoudeni Basin may be permissive. Known magmatic Cu-Ni deposits of these types in Mauritania are few in number and some uncertainty exists as to the nature of several of the more important ones.

Open-File Report↗

USGS1977

Genesis of a zoned granite stock, Seward Peninsula, Alaska

A composite epizonal stock of biotite granite has intruded a diverse assemblage of metamorphic rocks in the Serpentine Hot Springs area of north-central Seward Peninsula, Alaska. The metamorphic rocks include amphibolite-facies orthogneiss and paragneiss, greenschist-facies fine-grained siliceous and graphitic metasediments, and a variety of carbonate rocks. Lithologic units within the metamorphic terrane trend generally north-northeast and dip moderately toward the southeast. Thrust faults locally juxtapose lithologic units in the metamorphic assemblage, and normal faults displace both the metamorphic rocks and some parts of the granite stock. The gneisses and graphitic metasediments are believed to be late Precambrian in age, but the carbonate rocks are in part Paleozoic. Dating by the potassium-argon method indicates that the granite stock is Late Cretaceous. The stock has sharp discordant contacts, beyond which is a well-developed thermal aureole with rocks of hornblende hornfels facies. The average mode of the granite is 29 percent plagioclase, 31 percent quartz, 36 percent K-feldspar, and 4 percent biotite. Accessory minerals include apatite, magnetite, sphene, allanite, and zircon. Late-stage or deuteric minerals include muscovite, fluorite, tourmaline, quartz, and albite. The stock is a zoned complex containing rocks with several textural facies that are present in four partly concentric zones. Zone 1 is a discontinuous border unit, containing fine- to coarse-grained biotite granite, that grades inward into zone 2. Zone 2 consists of porphyritic biotite granite with oriented phenocrysts of pinkish-gray microcline in a coarse-grained equigranular groundmass of plagioclase, quartz, and biotite. It is in sharp, concordant to discordant contact with rocks of zone 3. Zone 3 consists of seriate-textured biotite granite that has been intruded by bodies of porphyritic biotite granite containing phenocrysts of plagioclase, K-feldspar, quartz, and biotite in an aplitic groundmass. Flow structures, pegmatite and aplite segregations, and miarolitic cavities are common in the seriate-textured granite. Zone 4, which forms the central part of the complex, consists of fine- to medium-grained biotite granite and locally developed leucogranite. Small miarolitic cavities are common within it. Eight textural facies have been defined within the complex, and mineralogic, petrographic, modal, and chemical variations are broadly systematic within the facies sequence. Study of these variations shows that the gradational facies of zones l and 2 systematically shift toward more mafic compositions inward within the complex. Seriate-textured rocks of zone 3 are similar in composition to those of zone 2, but porphyritic rocks of zone 3 and rocks of zone 4 mark shifts to more felsic compositions. These late-crystallizing felsic rocks are products of an interior residual magma system. This system was enriched in water and certain trace elements including tin, lithium, niobium, lead, and zinc. The complex as a whole has higher concentrations of these elements than many other granites. The nature of this geochemical specialization is particularly well demonstrated by the trace-element composition of biotite. The crystallization history of the pluton was complex. The available data suggest that this history could have included: (1) chilling and metasomatic alteration adjacent to the contact, (2) in-situ crystallization in several marginal facies accompanied by some transfer of residual constituents toward interior parts of the pluton, (3) slight upward displacement of magma that was subjacent to the crystallized walls, accompanied by disequilibrium crystallization and local vapor saturation, (4) upward displacement of part of the residual water-rich interior magma, accompanied by rapid loss of a separated vapor phase, and (5) displacement of the margins of the pluton by normal faults, accompanied by loss of an exsolved vapor phase from th

Open-File Report↗

USGS1981

Alkalic rocks and resources of thorium and associated elements in the Powderhorn District, Gunnison County, Colorado

Alkalic igneous rocks and related concentrations of thorium, niobium, rare-earth elements, titanium, and other elements have long been known in the Powderhorn mining district and have been explored intermittently for several decades. The deposits formed chiefly about 570 m.y. (million years) ago in latest Precambrian or Early Cambrian time. They were emplaced in lower Proterozoic (Proterozoic X) metasedimentary, metavolcanic, and plutonic rocks. The complex of alkalic rocks of Iron Hill occupies 31 km 2 (square kilometers) and is composed of pyroxenite, uncompahgrite, ijolite, nepheline syenite, and carbonatite, in order of generally decreasing age. Fenite occurs in a zone, in places more than 0.6 km (kilometer) wide, around a large part of the margin of the complex and adjacent to alkalic dikes intruding Precambrian host rock. The alkalic rocks have a radioactivity, chiefly due to thorium, greater than that of the surrounding Powderhorn Granite (Proterozoic X) and metamorphic rocks. The pyroxenite, uncompahgrite, ijolite, and nepheline syenite, which form more than 80 percent of the complex, have fairly uniform radioactivity. Radioactivity in the carbonatite stock, carbonatite dikes, and the carbonatite-pyroxenite mixed rock zone, however, generally exceeds that in the other rocks of the complex. The thorium concentrations in the Powderhorn district occur in six types of deposits: thorite veins, a large massive carbonatite body, carbonatite dikes, trachyte dikes, magnetite-ilmeniteperovskite dikes or segregations, and disseminations in small, anomalously radioactive plutons chiefly of granite or quartz syenite that are older than rocks of the alkalic complex. The highest grade thorium concentrations in the district are in veins that commonly occur in steeply dipping, crosscutting shear or breccia zones in the Precambrian rocks. They range in thickness from a centimeter or less to 5 m (meters) and are as much as 1 km long. The thorite veins are composed chiefly of potassic feldspar, white to smoky quartz, calcite, barite, goethite, and hematite, and also contain thorite, jasper, magnetite, pyrite, galena, chalcopyrite, sphalerite, synchysite, apatite, fluorite, biotite, sodic amphibole, rutile, monazite, bastnaesite, and vanadinite. The Th0 2 content of the thorite veins ranges from less than 0.01 percent to as much as 4.9 percent in high-grade samples. The Th0 2 content is generally less than 1 percent, however, and is only 0.05 to 0.1 percent in many of the veins examined in the district. Samples of the dolomitic carbonatite of Iron Hill mostly range from 3 to 145 ppm (parts per million) thorium. Thirty samples of the carbonatite dikes, the most radioactive rocks within the complex of Iron Hill, contain about 30 to 3,200 ppm thorium and a trace to about 1.5 percent rare-earth oxides. The magnetite-ilmenite-perovskite rocks have a radioactivity of 2 to 12 times the background of Precambrian granite that is attributable chiefly to thorium substitution for calcium in the perovskite. In two analyses the perovskite contains 0.12 and 0.15 percent Th0 2 . Trachyte dikes as much as 25 m thick cut the Precambrian rocks; their radioactivity is generally about two to four times the background of typical Precambrian granite, is locally higher, but is low relative to other types of thorium concentrations. A finegrained granite that is anomalously radioactive occurs in thick, dikelike plutons as much as 1.2 km wide, or more. The thorium content varies widely within the granite bodies. Eight samples of the granite contain 32 to 281 ppm thorium (averaging 115 ppm). The economic potential of thorium in the Powderhorn district is related in part to other elements such as niobium, titanium, iron, and rare earths. The proportions of niobium and rare earths to thorium vary in different parts of the district. Within the carbonatite body of Iron Hill, the Nb 2 0 5 content greatly exceeds Th0 2 , but the Th0 2 -Nb 2 0 5

Professional Paper↗

USGS2013

Reconnaissance geologic map of the Kuskokwim Bay region, southwest Alaska

The rocks of the map area range from Proterozoic age metamorphic rocks of the Kanektok metamorphic complex (Kilbuck terrane) to Quaternary age mafic volcanic rocks of Nunivak Island. The map area encompasses much of the type area of the Togiak-Tikchik Complex. The geologic maps used to construct this compilation were, for the most part, reconnaissance studies done in the time period from the 1950s to 1990s. Pioneering work in the map area by J.M. Hoare and W.L. Coonrad forms the basis for much of this map, either directly or as the stepping off point for later studies compiled here. Physiographically, the map area ranges from glaciated mountains, as much as 1,500 m high, in the Ahklun Mountains to the coastal lowlands of northern Bristol Bay and the Kuskokwim River delta. The mountains and the finger lakes (drowned fiords) on the east have been strongly affected by Pleistocene and Holocene glaciation. Within the map area are a number of major faults. The Togiak-Tikchik Fault and its extension to the northeast, the Holitna Fault, are considered extensions of the Denali fault system of central Alaska. Other sub-parallel faults include the Golden Gate, Sawpit, Goodnews, and East Kulukak Faults. Northwest-trending strike-slip faults crosscut and offset northeast-trending fault systems. Rocks of the area are assigned to a number of distinctive lithologic packages. Most distinctive among these packages are the high-grade metamorphic rocks of the Kanektok metamorphic complex or Kilbuck terrane, composed of a high-grade metamorphic orthogneiss core surrounded by greenschist and amphibolite facies schist, gneiss, and rare marble and quartzite. These rocks have yielded radiometric ages strongly suggestive of a 2.05 Ga emplacement age. Poorly known Paleozoic rocks, including Ordovician to Devonian and Permian limestone, are found east of the Kanektok metamorphic complex. A Triassic(?) ophiolite complex is on the southeast side of Kuskokwim Bay; otherwise only minor Triassic rock units are known. The most widespread rocks of the area are Jurassic and Early Cretaceous(?) volcanic and volcaniclastic rocks. The Kuskokwim Group flysch is restricted largely to the northeast part of the map area. It consists primarily of shelf and minor nearshore facies rocks. Primarily exposed in the lowlands west of the Ahklun Mountains, extensive latest Tertiary and Quaternary alkalic basalt flows and lesser pyroclastic rocks form much of the bedrock of the remaining area. On Saint Matthew Island, Cretaceous volcanic and pyroclastic rocks occur that are not found elsewhere within the map area. The Kuskokwim Group and older rocks, including on Saint Matthew Island, but not the Kanektok metamorphic complex, are intruded by widely dispersed Late Cretaceous and (or) Early Tertiary granitic rocks. Much of the lowland area is mantled by unconsolidated deposits that include glacial, alluvial and fluvial, marine, estuarine, and eolian deposits. These formed during several episodes of Quaternary glaciation.

Alaska↗

USGS2024

Geologic map and structure sections along the southern part of the Bartlett Springs Fault Zone and adjacent areas from Cache Creek to Lake Berryessa, northern Coast Ranges, California

Introduction Located in the Coast Ranges of northern California, the Bartlett Springs Fault Zone is the easternmost fault in the San Andreas Fault system in northern California. The fault is a right-lateral, strike-slip structure considered capable of producing an earthquake of moment magnitude 7. The purpose of this mapping is to better characterize the geology and earthquake hazards associated with the southern part of the Bartlett Springs Fault Zone and to help identify any evidence of active uplift on the faults bounding the Coast Ranges. Although the area immediately surrounding the Bartlett Springs Fault Zone is sparsely populated, its southern segment presents a potential seismic hazard to northern California communities as far away as the San Francisco Bay region and Sacramento. There are also nearby water resources, mineral resources, and public lands used for public recreation. The Coast Ranges of northern California are a series of northwest-southeast-oriented mountain ranges and valleys located north of the San Francisco Bay region, between the Pacific Ocean to the west and the Sacramento Valley to the east. The region has rugged terrain, high mountain peaks that reach more than 2,400 meters above sea level, isolated and narrow valley bottoms on which most human settlements are located, and large drainage systems that tend to follow the northwest-southeast-oriented topographic grain. The physiographic character of the region is shaped by its bedrock geology, deformational history, and active faulting. The basement rocks of the northern Coast Ranges consist of the Franciscan Complex and the Great Valley complex, the latter of which consists of two informal units, the Coast Range ophiolite and the Great Valley sequence. The Franciscan Complex and the Great Valley complex are in structural contact along the Coast Range Fault, a regional-scale structure and fundamental crustal boundary. The Franciscan Complex and the Great Valley complex are superposed by active, northwest-southeast-striking strike-slip faults that are associated with seismicity swarms. These active strike-slip faults can produce moderate to large earthquakes that have moment magnitudes of 7–8. In places, these active structures bound large ranges and valleys, suggesting that much of the modern topographic expression is the result of active deformation processes. This report contains new 1:24,000-scale geologic mapping along the southern part of the Bartlett Springs Fault Zone between Clear Lake and Lake Berryessa. The map area spans 738 square kilometers in northern Napa County, southern Lake County, and parts of Yolo and Colusa Counties. The south and east borders of the map are 90 kilometers north of San Francisco and 70 kilometers west of Sacramento, respectively. The map area is within the Knoxville mining district, which has a history of mercury and gold mining dating back to the mid-19th century. The two main towns in the region, Lower Lake and Clearlake, California, are west-northwest of the map area. Approximately 71,000 people live in the cities and rural communities located within a 40-kilometer radius of the center of the map area. The bedrock geology, cross sections, and structural data presented herein are critical for evaluating the long-term evolution of the Bartlett Springs Fault Zone. This work will supplement studies on local seismic hazards, liquefaction potential, landslide hazards, earthquake geology, natural resources, groundwater resources, engineering geology, and tectonic history by providing the background information for site-specific investigations on these subjects.

California↗

USGS2014

Vegetation changes associated with a population irruption by Roosevelt elk

Interactions between large herbivores and their food supply are central to the study of population dynamics. We assessed temporal and spatial patterns in meadow plant biomass over a 23-year period for meadow complexes that were spatially linked to three distinct populations of Roosevelt elk (Cervus elaphus roosevelti) in northwestern California. Our objectives were to determine whether the plant community exhibited a tolerant or resistant response when elk population growth became irruptive. Plant biomass for the three meadow complexes inhabited by the elk populations was measured using Normalized Difference Vegetation Index (NDVI), which was derived from Landsat 5 Thematic Mapper imagery. Elk populations exhibited different patterns of growth through the time series, whereby one population underwent a complete four-stage irruptive growth pattern while the other two did not. Temporal changes in NDVI for the meadow complex used by the irruptive population suggested a decline in forage biomass during the end of the dry season and a temporal decline in spatial variation of NDVI at the peak of plant biomass in May. Conversely, no such patterns were detected in the meadow complexes inhabited by the nonirruptive populations. Our findings suggest that the meadow complex used by the irruptive elk population may have undergone changes in plant community composition favoring plants that were resistant to elk grazing.

Ecology and Evolution↗