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At least 1,423 records · Page 79Linked to original sources
USGS1952

Magmatic differentiation in tertiary and quaternary volcanic rocks from Adak and Kanaga Islands, Aleutian Islands, Alaska

Samples of 17 volcanic rocks of Tertiary and Quaternary age from Adak and Kanaga islands have been chemically analyzed and studied microscopically. Spectrograms have been made of 10 of them. The rocks from Adak represent one center of possibly older Tertiary age and two centers of younger Tertiary or Quaternary age. The rocks from Kanaga Island represent both a shield volcano of possibly Tertiary age, partly destroyed by the formation of a caldera, and a young cone of Quaternary age that has grown within the caldera. All the rocks are basalt or andesite. Modally, all are characterized by relatively large crystals of plagioclase more calcic than andesine, and by one or more of the following ferromagnesian minerals: olivine, hypersthene, augite, and hornblende. Apatite and iron ores are common, and late silica minerals and orthoclase occur interstitially in the groundmasses of some rocks . As analyses of no more than four samples are available for each center, the small differences between sets of analyses representing different centers are of doubtful significance. Consequently, the analyses representing all the centers have been plotted on each of the several diagrams used. The several types of variation diagrams show that the province is a calc-alkaline one. The alkali-lime index is in the neighborhood of 63. This very high value is comparable with that for Katmai and is only slightly less than the maximum for the Japanese volcanic rock series. The quantities of minor constituents present are not exceptional for the rock types analyzed; the rocks from Adak are apparently more strontium-rich than those from Kanaga . The chemical analyses of the more basic rock types, as compared with the average analysis of plateau basalt, suggest that the Aleutian parental magma could have been derived from a plateau basalt magma by the addition of plagioclase and the subtraction of pyroxene, iron ore, and some quartz. The distribution of the minor elements can be explained more easily by postulating that, at least on Kanaga Island , some sediments have been assimilated. The derivation of the analyzed rocks from the Aleutian parental magma is most easily explained by the hypothesis that the plagioclase remained in suspension while the ferromagnesian minerals were settling out.

Alaska↗
USGS1974

Correlation between geophysical data and rock types in the Piedmont and coastal plain of northeast Virginia and related areas

Physical, chemical, and mineralogic characteristics of rock units in parts of the northeast Virginia Piedmont are reflected in the aeromagnelic, aeroradioactivity, and gravity data for this area. Magnetic anomalies show the areal distribution of rocks containing magnetite. Aeroradiometric anomalies in the Piedmont and Coastal Plain provinces are directly related to the K 2 O content of the formations. In the crystalline rocks of the Piedmont this is reflected in their muscovite and microcline content, whereas in the Coastal Plain province it is related to the glauconite content of the Aquia Formation. Locally, in the crystalline rocks of the Piedmont, uranium- and thorium-bearing mineral content is of greater importance than K 2 O-bearing mineral content in producing aeroradiometric anomalies. The region also is characterized by (1) a northern gravity high, (2) a southern gravity high presumed to be caused by mafic rocks, and (3) an intervening zone characterized by low gravity relief and underlain by schist and gneiss. Geologic and geophysical extrapolation southward toward the Arvonia area show that the Chopawamsic Formation and the volcanic rocks of the Evington group are coeval. Also, on the northwest side of these volcanic rocks is a belt of small rootless mafic and ultramafic rocks diapirically ceplaced in folded rocks of Early Cambrian (?) age.

Virginia↗
USGS1968

Exploration possibilities in the Western Chagai District, West Pakistan

A northerly-trending group of quartz diorite stocks that cut Cretaceous, Eocene, 01igocene(?) and Pleistocene( ?) sedimentary rocks near Saindak, West Pakistan , contain oxidized disseminated copper minerals which may occur in commercial concentrations at depth. The stocks are enclosed by an aureole of albite-epidote hornfels about 4 miles wide that locally is cut by veins containing sparse lead and copper minerals. Within the contact aureole the few thin beds of limestone and lenticular limestone reefs have been metasomatically replaced by iron sulfide or iron oxide. The sulfide is largely oxidized near the surface. The areas of metamorphosed rocks to which the veins are mostly restricted can be recognized on panchromatic aerial photographs and from a considerable distance on the ground by their rugged topography, dark color, and by the local abundance of dikes, thus greatly reducing the area requiring field examination during a prospecting program. The red and yellow soils mantling the sulfide-rich rocks are easily recognized from short distances on the ground, but cannot be differentiated from the unmetamorphosed rocks on conventional aerial photographs. Color photography or limited-spectral photo techniques probably can be used to reveal these distinctive soils and thus define the areas of sulfide mineralization.

west Pakistan↗
USGS2008

Questa baseline and pre-mining ground-water quality investigation. 17. Geomorphology of the Red River Valley, Taos County, New Mexico, and influence on ground-water flow in the shallow alluvial aquifer

In April 2001, the U.S. Geological Survey (USGS) and the New Mexico Environment Department (NMED) began a cooperative study to infer the pre-mining ground-water chemistry at the Molycorp molybdenum mine site in the Red River Valley of north-central New Mexico. This report is one in a series of reports that can be used to determine pre-mining ground-water conditions at the mine site. Molycorp’s Questa molybdenum mine in the Red River Valley, northern New Mexico, is located near the margin of the Questa caldera in a highly mineralized region. The bedrock of the Taos Range surrounding the Red River is composed of Proterozoic rocks of various types, which are intruded and overlain by Oligocene volcanic rocks associated with the Questa caldera. Locally, these rocks were altered by hydrothermal activity. The alteration zones that contain sulfide minerals are particularly important because they constitute the commercial ore bodies of the region and, where exposed to weathering, form sites of rapid erosion referred to as alteration scars. Over the past thousand years, if not over the entire Holocene, erosion rates were spatially variable. Forested hillslopes eroded at about 0.04 millimeter per year, whereas alteration scars eroded at about 2.7 millimeters per year. The erosion rate of the alteration scars is unusually rapid for naturally occurring sites that have not been disturbed by humans. Watersheds containing large alteration scars delivered more sediment to the Red River Valley than the Red River could remove. Consequently, large debris fans, as much as 80 meters thick, developed within the valley. The geomorphology of the Red River Valley has had several large influences on the hydrology of the shallow alluvial aquifer, and those influences were in effect before the onset of mining within the watershed. Several reaches where alluvial ground water emerges to become Red River streamflow were observed by a tracer dilution study conducted in 2001. The aquifer narrows where erosion-resistant bedrock, which tends to form vertical cliffs, restricts the width of the valley bottom. Although the presence of a shallow bedrock sill, overlain by shallow alluvium, is a plausible cause of ground-water emergence, this cause was not demonstrated in the study area. The water-table gradient can locally decrease in the downstream direction because of changes in the hydraulic properties of the alluvium, and this may be a contributing cause of ground-water emergence. However, at one site (near Cabin Springs), ground-water emergence could not be explained by spatial changes in geometric or hydraulic properties of the aquifer. Furthermore, the available evidence demonstrates that ground water flowing through bedrock fractures or colluvium entered the north side of the alluvial aquifer, and is the cause of ground-water emergence. At that location the alluvial aquifer was already flowing full, causing the excess water to emerge into the stream. An indirect consequence of altered rock in the tributary watersheds is the rapid erosion rate of alteration scars combined with the hydraulic properties of sediments shed from those scars. Where alteration scars are large the debris fans at the mouths of the tributary watersheds substantially encroach into the Red River Valley. At such locations debris-fan materials dominate the width and thickness of the alluvium in the valley and reduce the rate of flow of ground water within the Red River alluvial aquifer. Most sites of groundwater emergence are located immediately upstream from or along the margins of debris fans. A substantial fraction of the ground water approaching a debris fan can emerge to become streamflow. This last observation has three implications. First, very little water can flow the entire length of the study area entirely within the alluvial aquifer because the ground water repeatedly contacts debris-fan sediments over that length. Second, it follows that emerging water containing unique elemental constituents must have entered the alluvial aquifer at a relatively short distance upstream. Third, a gravel aquifer downstream from a large debris fan can transmit more ground water than flows into it through the debris fan. This observation explains how the water table can be naturally, and permanently, located well beneath the level of the bed of a perennial stream.

New Mexico↗
USGS1991

Marion Peak quadrangle, Fresno County, California— Analytic data

The Marion Peak 15-minute quadrangle includes about 620 km2 on the west slope of the Sierra Nevada in Fresno County, California, between 36°45' and 37°00' N. latitude and 118°30' and 118°45 W. longitude. This report supplements the geologic map of the Marion Peak quadrangle by providing modal and chemical analyses of the granitic and volcanic rock samples. Granitic rocks of the batholith underlie 95 percent of the quadrangle area. Most of the remaining area is underlain by septa of pre-batholithic metamorphosed sediments and volcanic rocks which occur between the individual granitic masses. Cenozoic volcanic rocks underlie a small area, and they include an eroded dacitic volcanic center and scattered erosional remnants of basaltic lava flows. About 300 samples of typical plutonic and volcanic rocks were collected during the course of geologic mapping; of these, 30 granitic, 2 metavolcanic, and 9 Cenozoic volcanic rocks were chemically analyzed for their major elements, and most were also analyzed for selected trace elements. In addition, 178 samples of granitic rocks were analyzed modally for the volume percent of their constituent minerals. Measurements of specific gravity and magnetic susceptibility are also included. The average chemical composition of the granitic rocks in the quadrangle, estimated from the analyzed samples, is a silicic granodiorite that contains 69.2 weight percent SiO 2 .

California↗
USGS1999

Syngenetic Au on the Carlin trend: Implications for Carlin-type deposits

A new type of gold occurrence recently discovered in the Carlin trend, north-central Nevada, is clearly distinct from classic Carlin-type gold ore. These occurrences are interpreted to be of sedimentary exhalative (sedex) origin because they are stratiform and predate compaction and lithification of their unaltered Devonian host rocks. They contain barite that exhibits δ 34 S and δ 18 0 values identical to sulfate in Late Devonian seawater and sedex-type barite deposits. Abrupt facies changes in the host rocks strongly suggest synsedimentary faulting and foundering of the carbonate shelf during mineralization, as is characteristic of sedex deposits. Gold occurs both as native inclusions in synsedimentary base-metal sulfides and barite, and as chemical enrichments in sulfide minerals. The absence of alteration and lack of δ 13 C and δ 18 0 isotopic shift of primary carbonates in these rocks is strong evidence that this gold was not introduced with classic Carlin-type mineralization. Collectively, these features show that the Devonian strata were significantly enriched in gold some 300 m.y. prior to generation of the mid-Tertiary Carlin-type deposits. These strata may have been an important, perhaps even vital, source of gold for the latter. Although gold is typically low in most Zn-Pb-rich sedex deposits, our evidence suggests that transport of gold in basinal fluids, and its subsequent deposition in the sedex environment, can be significant.

Geology↗
USGS1954

The East Slope No. 2 uranium prospect, Piute County, Utah

The secondary uranium minerals autunite, metatorbernite, uranophane(?), and schroeckingerite occur in altered hornfels at the East Slope No. 9. uranium prospect. The deposit, in sec. 6, T. 9.7 S., R. 3 W., Piute County, Utah, is about 1 mile west of the Bullion Monarch mine which is in the central producing area of the Marysvale uranium district. Hornfels, formed by contact metamorphism of rocks of the Bullion Canyon volcanics borderhug the margin of a quartz monzonite stock, is in fault contact with the later Mount Belknap rhyolite. The hornfels was intensely altered by hydrothermal solutions in pre-Mount Belknap time. Hematite-alunite-quartz-kaolinite rock, the most completely altered hornfels, is surrounded by orange to white argillized hornfels containing beidellite-montmorillonite clay, and secondary uranium minerals. The secondary uranium minerals probably have been derived from pitchblende, the primary ore mineral in other deposits of the Marysvale area. The two uranium-rich zones, 4 feet ad 5 feet thick, have been traced on the surface for 60 feet and 110 feet, respectively. Channel samples from these zones contained as much as 0.047 percent uranium. The deposit is significant because of its position outside the central producing area and because of the association of uranium minerals with alunitic rock in hydrothermally altered hornfels of volcanic rocks of early Tertiary age.

Circular↗
USGS2012

Hydrous carbonates on Mars?: Evidence from Mariner 6/7 infrared spectrometer and ground‐based telescopic spectra

Absorption features at 2.28 and 5.4 μm identified in Mariner 6/7 infrared spectrometer and terrestrial telescopic spectra are consistent with the spectra of hydrous magnesium carbonates such as hydromagnesite and artinite. Spectral characteristics of these hydrous carbonates are different from those of the anhydrous carbonates, as the former do not have the strong spectral features typically associated with anhydrous carbonates such as calcite and siderite. Theoretical mixing indicates that, depending on the type of hydrous carbonate, 10–20 wt % can be incorporated into the regolith without contradicting the spectral observations or the Viking x ray fluorescence chemical analysis. Hydrous carbonates form as weathering products of mafic minerals in the presence of H 2 O and CO 2 , even in the Antarctic. Their formation as evaporite minerals from either original magmas or hydrothermally altered rocks is consistent with the Martian environment, provided liquid water is or has been at least transiently present. On Earth, formation of hydrous Mg carbonates is associated with the production of amorphous iron oxides, which is consistent with both the environment and the inferred surface mineralogy of Mars. These minerals are about 60 wt % H 2 O, CO 3 , and OH; if they are abundant everywhere at the 10% level, then about 6% of the surface weight could be volatiles bound in this type of mineral. Although the stability of hydrous carbonates in a Martian environment is uncertain, there may be kinetic factors inhibiting the dehydration of these minerals, which may persist metastably in the current environment. Although the spectroscopic evidence for anhydrous carbonates is scant, the possible presence of hydrous carbonates provides an appealing mechanism for the existence of carbonates on Mars.

Journal of Geophysical Research↗
USGS2013

Trace metal-rich Quaternary hydrothermal manganese oxide and barite deposit, Milos Island, Greece

The Cape Vani Mn oxide and barite deposit on Milos Island offers an excellent opportunity to study the three-dimensional characteristics of a shallow-water hydrothermal system. Milos Island is part of the active Aegean volcanic arc. A 1 km long basin located between two dacitic domes in northwest Milos is filled with a 35-50 m thick section of Quaternary volcaniclastic and pyroclastic rocks capped by reef limestone that were hydrothermally mineralized by Mn oxides and barite. Manganese occurs as thin layers, as cement of sandstone and as metasomatic replacement of the limestone, including abundant fossil shells. Manganese minerals include chiefly δ-MnO2, pyrolusite and ramsdellite. The MnO contents for single beds range up to 60%. The Mn oxide deposits are rich in Pb (to 3.4%), BaO (to 3.1%), Zn (to 0.8%), As (to 0.3%), Sb (to 0.2%) and Ag (to 10 ppm). Strontium isotopic compositions of the Mn oxide deposits and sulphur isotopic compositions of the associated barite show that the mineralizing fluids were predominantly sea water. The Mn oxide deposit formed in close geographical proximity to sulphide-sulphate-Au-Ag deposits and the two deposit types probably formed from the same hydrothermal system. Precipitation of Mn oxide took place at shallow burial depths and was promoted by the mixing of modified sea water (hydrothermal fluid) from which the sulphides precipitated at depth and sea water that penetrated along faults and fractures in the Cape Vani volcaniclastic and tuff deposits. The hydrothermal fluid was formed from predominantly sea water that was enriched in metals leached from the basement and overlying volcanogenic rocks. The hydrothermal fluids were driven by convection sustained by heat from cooling magma chambers. Barite was deposited throughout the time of Mn oxide mineralization, which occurred in at least two episodes. Manganese mineralization occurred by both focused and diffuse flow, the fluids mineralizing the beds of greatest porosity and filling dilatational fractures along with barite.

Milos Island↗
USGS1971

Sulfur isotope study of the "B" limestone and Galena fissure ore deposits of the U.S. mine, Bingham mining district, Utah

The delta S 34 values for 261 sulfide concentrates from the "B" limestone replacement and Galena fissure deposits of the U. S. mine range from +3.8 to --8.0 permil; the mean is +0.56 permil. The data indicate that (1) sulfides of the "B" limestone ore deposits are depleted in S 34 by 0.4 to 0.7 permil relative to those of the Galena fissure ore deposits; (2) sulfides of both deposits exhibit a primary fractionation trend characterized by increasing S 34 depletion in the sequence pyrite, sphalerite, tetrahedrite, and galena; (3) delta values for coexisting sulfide pairs of the "B" limestone deposit increase with increasing altitude; (4) sulfides of both deposits are increasingly depleted in S 34 with increasing altitude; (5) the paragenetic order of sulfide deposition is accompanied by an apparent depletion of S 34 that is independent of mineral species; and (6) pyrite disseminated in wall rocks is depleted in S 34 relative to pyrite from adjacent ore deposits. The similarity of delta S 34 values and isotopic trends to those of the central porphyry-type deposit at Bingham (Field, 1966) suggests that the hydrothermal deposits of the district were formed by fluids that originated from a common source during one episode of sequential mineralization. Gross isotopic differences between the deposits, consistent differences between coexisting sulfides, and systematic variations of delta values are attributed to temperature effects imposed upon sulfide exchange equilibria; isotopic temperatures suggest a lateral gradient between the "B" limestone and adjacent Galena fissure deposits and a possible vertical gradient within the "B" limestone deposit. The vertical zonation of delta S 34 values and trends related to pyrite physical occurrence and sulfide paragenesis are provisionally attributed to a pH-Eh control. Although the apparent trends are imperfectly resolved because of textural complexities, the marked depletion of S 34 in pyrite disseminated in country rocks warrants additional study as a potential exploration method.

Utah↗
USGS2017

Multiscale hyperspectral imaging of the Orange Hill Porphyry Copper Deposit, Alaska, USA, with laboratory-, field-, and aircraft-based imaging spectrometers

In the past decade, use of hyperspectral imaging (imaging spectroscopy) for mineral exploration and mining operations has been increasing at different spatial scales. In this paper, we focus on recent trends in applying imaging spectrometer data to: 1) airborne imaging of high latitude deposits, 2) field-based imaging of outcrops, and 3) laboratory-level imaging of geologic samples. Comparing mineral information derived from imaging spectrometer data acquired at these three scales in Alaska in areas of exposed porphyry Cu-Au-Mo deposits, Orange Hill and Bond Creek, we find notable consistency in identifications of spectrally predominant minerals, including white mica, chlorite, clays, and gypsum. Variations in the wavelength position of white mica 2200 nm Al-OH absorption seen at the airborne level are echoed by finerscale field and laboratory imaging, with wavelength positions spanning the 2199 to 2207 nm range. The longerwavelength micas associated with porphyry formation are more phengitic in composition, and thus distinct from mica in plutonic and volcanic arc rocks not affected by magmatic-hydrothermal fluids. The hillside imagery, collected on a cloudy day that would have precluded aircraft survey, gave comparable result to airborne and laboratory data, indicating field-based imaging spectroscopy can be a feasible alternative to airborne survey for accessible targets. Direct spectral observation of molybdenite in rocks collected from the Orange Hill deposit demonstratesthat additional important mineral information can be revealed with laboratory level imaging spectroscopy that is difficult to obtain in coarser scale data, commonly due to low areal extent of target minerals. The spatial association of the clinochlore + white mica and long wavelength white mica spectral classes to multi-element Cu-Mo-Au anomalies from geochemical analyses of rocks and sediments support a causative relationship with magmatic-hydrothermal alteration. Mineral maps from the airborne data were used to guide field sampling that found additional CuMo-Au mineralized areas, which were previously unknown or unreported. The results from this study provide support for utilization of imaging spectroscopy for assisting mineral exploration in other portions of the state of Alaska as well as other areas at high latitudes. Imaging spectroscopy has the potential to provide targeting information for follow-up sampling and investigations, potentially reducing subsequent exploration costs.

Alaska↗
USGS1990

An evaluation and geochemical survey of the Farah Garan East Prospect, Southeast Asir, Kingdom of Saudi Arabia

The Farah Garan East prospect (MODS 4886) is located in the southeastern part of the Precambrian Arabian Shield of Saudi Arabia, about 15 km east-northeast of Zahran Al Janub and 1 km northeast of the ancient mines at Farah Garan. Ore minerals at the Farah Garan East prospect are pyrite, tennantite, galena, and sphalerite. These are sparsely and erratically distributed in west-dipping beds of dolomite, dolomite-talc breccia, and carbonate-sericite phyllite, and in associated breccias and zones of carbonate-altered mafic metavolcanic rocks, all of Precambrian age. Concordant beds of dolomite and carbonate-sericite phyllite are interlayered with metavolcanic rocks and are interpreted as volcanic-related submarine hydrothermal deposits of Precambrian age. Funnel-shaped bodies of dolomite-talc breccia that crop out near the north and south ends of the dolomite beds are interpreted as submarine hot-spring vent breccias. Aprons of exhalative dolomite thin laterally outward from these vents. Discordant and concordant zones of carbonate-altered metavolcanic rocks, east of and structurally below the hot-spring vents, probably represent pathways of hydrothermal circulation along networks of fractures in volcanic rocks, subjacent to these Precambrian submarine hot-spring vents. Ore minerals in outcrops, and geochemically anomalous concentrations of gold, silver, copper, lead, zinc, arsenic, antimony, and tellurium are present in carbonate-rich rocks of the hot-spring assemblage. This indicates that the ore minerals and elements were deposited originally as constituents of the hot-spring assemblage. However, exposed ore-mineral occurrences are small and sparse, and geochemical anomalies are small, irregularly distributed, and of subeconomic grade. Furthermore, weak electromagnetic anomalies do not indicate the presence of subsurface bodies of concentrated, conductive ore minerals. Therefore, no drilling is recommended.

Open-File Report↗
USGS2026

Integrating detrital magnetite geochemistry and (U-Th)/He chronometry as a sediment provenance tool in geologic and metallogenic terranes

Magnetite is ubiquitous in porphyry Cu systems and in sediment sourcing both barren and mineralized regions, with potential as an indicator mineral in concealed and coarsely-mapped terranes. We develop and test a workflow for integrated geochemistry and (U–Th)/He (He) dating for inferring detrital magnetite (DMt) provenance in these settings. The ca. 70 Ma Taurus porphyry Cu–Mo(–Au) district in eastern interior Alaska serves as a test case. DMt from streams draining porphyry-related mineralization was characterized by geochemistry and mineral inclusion and microstructure observations, complemented by similar data for potential porphyry and host rock sources. Principal component analysis and clustering of DMt geochemical data resolve multiple populations in our samples geochemically and texturally compatible with derivation from metamorphic, porphyry-related hydrothermal, and igneous sources. Hydrothermal magnetite comprises ∼16–50% of DMt nearest porphyry mineralization but diminishes to ∼4% ∼15 km downstream. Subsampled grains within populations yield ∼160–110 Ma, ∼70 Ma, ∼55 Ma, and ∼20 Ma magnetite He date modes. Combined with provenance, He dates capture Early Cretaceous regional exhumation of metamorphic host rock and Late Cretaceous porphyry Cu mineralization. DMt grains showing partial hematite replacement yield ca. 55–20 Ma dates regardless of source, overlapping regional warm/wet climatic intervals. We interpret Cenozoic dates to reflect exhumation to near-surface oxidizing conditions and(or) supergene weathering. Magnetite is thus a promising target phase for (1) tracking the spatiotemporal distribution of porphyry systems, and (2) linking the formation and exhumation of these systems to a regional geologic history, both in Alaska and globally.

Alaska, Yukon↗
USGS1979

Occurrence of uranium in rocks of the intrusive complex at Ekiek Creek, western Alaska

Uranium in the Ekiek Creek Complex of western Alaska is related to a niobium-rich pyrochlore in the nepheline syenite of the complex. The complex consists of an aegirine-phlogopite pyroxenite that has been intruded and partly replaced by nepheline syenite. The contact zone between the two igneous units varies from a sharp contact to a diffuse zone where the pyroxenite has been metasomatically replaced by the syenite. The entire complex was intruded into an older Cretaceous monzonite. The pyrochlore occurs as an accessory mineral in the syenite, and is visible in rocks containing over 50 ppm uranium. Chemical analyses indicate that, in all samples of syenite, there is a positive correlation between uranium and niobium; this suggests that the uranium-pyrochlore association persists even when pyrochlore is not readily visible in thin section. The small amount of pyrochlore, and its refractory nature, make the complex an unfavorable source for secondary uranium leaching or heavy-mineral concentration.

Open-File Report↗
USGS1975

Interstitial solutions and diagenesis in deeply buried marine sediments: Results from the Deep Sea Drilling Project

Through the Deep Sea Drilling Project samples of interstitial solutions of deeply buried marine sediments throughout the World Ocean have been obtained and analyzed. The studies have shown that in all but the most slowly deposited sediments pore fluids exhibit changes in composition upon burial. These changes can be grouped into a few consistent patterns that facilitate identification of the diagenetic reactions occurring in the sediments. Pelagic clays and slowly deposited (<1 cm/10 3 yr) biogenic sediments are the only types that exhibit little evidence of reaction in the pore waters. In most biogenic sediments sea water undergoes considerable alteration. In sediments deposited at rates up to a few cm/10 3 yr the changes chiefly involve gains of Ca 2+ and Sr 2+ and losses of Mg 2+ which balance the Ca 2+ enrichment. The Ca-Mg substitution may often reach 30 mM/kg while Sr 2+ may be enriched 15-fold over sea water. These changes reflect recrystallization of biogenic calcite and the substitution of Mg 2+ for Ca 2+ during this reaction. The Ca-Mg-carbonate formed is most likely a dolomitic phase. A related but more complex pattern is found in carbonate sediments deposited at somewhat greater rates. Ca 2+ and Sr 2+ enrichment is again characteristic, but Mg 2+ losses exceed Ca 2+ gains with the excess being balanced by SO 4 post staggered2- losses. The data indicate that the reactions are similar to those noted above, except that the Ca 2+ released is not kept in solution but is precipitated by the HCO 3 post staggered- produced in SO 4 post staggered2- reduction. In both these types of pore waters Na + is usually conservative, but K + depletions are frequent. In several partly consolidated sediment sections approaching igneous basement contact, very marked interstitial calcium enrichment has been found (to 5.5 g/kg). These phenomena are marked by pronounced depletion in Na + , Si and CO 2 , and slight enhancement in Cl - . The changes are attributed to exchange of Na + for Ca 2+ in silicate minerals forming from submarine weathering of igneous rocks such as basalts. Water is also consumed in these reactions, accounting for minor increases in total interstitial salinity. Terrigenous, organic-rich sediments deposited rapidly along continental margins also exhibit significant evidences of alteration. Microbial reactions involving organic matter lead to complete removal of SO 4 post staggered2- , strong HCO 3 post staggered- enrichment, formation of NH 4 post staggered+ , and methane synthesis from H 2 and CO 2 once SO 4 post staggered2- is eliminated. K + and often Na + (slightly) are depleted in the interstitial waters. Ca 2+ depletion may occur owing to precipitation of CaCO 3 . In most cases interstitial Cl - remains relatively constant, but increases are noted over evaporitic strata, and decreases in interstitial Cl - are observed in some sediments adjacent to continents.

Geochimica et Cosmochimica Acta↗
USGS1993

Reconnaissance guidelines for gold exploration in Central Alaska

Distribution of more than 300 gold-bearing samples from the Livengood (Tolovana) and parts of the Fairbanks and Rampart mining districts in central Alaska, USA, indicate that the concentration of gold in placers is spatially related both to structural features and to Late Cretaceous and (or) Tertiary felsic plutons. The regional consistency of these spatial relationships is demonstrated by proximity analysis using a Geographic Information System (GIS), and suggests a genetic association between faults, felsic plutons, and gold occurrences. The local presence of gold within several of the plutons indicates that these are the source of some of the gold. In addition, some gold occurs proximal to faults where plutons are not present, suggesting that some of the gold was also derived from the country rock. We envision a model whereby weakly mineralized solutions, thermally driven by latent plutonic heat, were enriched by circulation through clastic units that may have had a naturally elevated gold background. The resultant enriched solutions were channeled and reconcentrated along or adjacent to large-scale fault systems. Future exploration to define individual target areas should be directed toward areas where Late Cretaceous and (or) Tertiary felsic plutons occur near major faults. ?? 1993.

Journal of Geochemical Exploration↗