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At least 127 records · Page 7Linked to original sources

USGS1974

Interstitial water studies on small core samples, Leg 22

Interstitial waters from Leg 22 in the Indian Ocean revealed two unique results: Site 214, on the Ninetyeast Ridge, penetrated through a 30-meter sequence of fine-grained basalt and reentered hard, silty clay containing carbonate skeletal debris. Such a basalt layer may well have been impervious and extensive enough to seal off underlying (fossil) seawater of Paleocene age. However, except for a marked increase in calcium and a slight increase in chloride, no appreciable changes in pore fluid chemistry could be confirmed. Site 217, at the northernmost end of the Ninetyeast Ridge, demonstrated record concentrations of interstitial calcium in clayey nannofossil oozes and a relatively small but significant increment in chloride with depth. Presumably, these increments signal the existence of evaporitic sediments or evaporite-influenced brines at considerably greater depth than penetrated.

Initial reports of the Deep Sea Drilling Project↗

USGS2003

Geologic framework and hydrogeologic features of the Glen Rose Limestone, Camp Bullis Training Site, Bexar County, Texas

The Glen Rose Limestone crops out over most of the Camp Bullis Training Site in northern Bexar County, Texas, where it consists of upper and lower members and composes the upper zone and the upper part of the middle zone of the Trinity aquifer. Uncharacteristically permeable in northern Bexar County, the Glen Rose Limestone can provide avenues for recharge to and potential contamination of the downgradient Edwards aquifer, which occupies the southeastern corner of Camp Bullis. The upper member of the Glen Rose Limestone characteristically is thin-bedded and composed mostly of soft limestone and marl, and the lower Glen Rose typically is composed mostly of relatively massive, fossiliferous limestone. The upper member, about 410 to 450 feet thick at Camp Bullis, was divided in this study into five hydrogeologic subdivisions, A through E (youngest to oldest). The approximately 120-foot-thick Interval A has an abundance of caves, which is indicative of its generally well developed fracture, channel, and cavern porosity that in places provides appreciable permeability. The 120- to 150-foot-thick Interval B is similar to Interval A but with less cave development and considerably less permeability. The 10- to 20-foot-thick Interval C, a layer of partly to mostly dissolved soluble carbonate minerals, is characterized by breccia porosity, boxwork permeability, and collapse structures that typically divert ground water laterally to discharge at land surface. The 135- to 180-foot-thick Interval D generally has low porosity and little permeability with some local exceptions, most notably the caprinid biostrome just below the top of the interval, which appears to be permeable by virtue of excellent moldic, vug, fracture, and cavern porosity. The 10- to 20-foot-thick Interval E, a layer of partly to mostly dissolved evaporites similar to Interval C, has similar hydrogeologic properties and a tendency to divert ground water laterally.

Texas↗

USGS1992

Mid-Mesozoic (Mid-Jurassic to Early Cretaceous) evolution of the Georges Bank Basin, U.S. North Atlantic outer continental shelf: Sedimentology of the Conoco 145-1 well

The Conoco 145-1 exploratory well, located in the southeastern portion of the Georges Bank Basin, was drilled to a total depth of 4303 m below the sea floor. The oldest sedimentary rocks sampled are of Middle Jurassic age (Late Bathonian-Callovian). A dolomite-limestone-evaporite sequence dominates the section below 3917 m; limestone is the predominant lithology in the intervals of 3271-3774 m, 2274-3158 m, and 1548-1981 m. Siliciclastics dominate the remainder of the drilled section. Calcite tightly cements most of the rocks below 1548 m; dolomite, silica, siderite, and diagenetic clay cements are locally important. Restricted inner marine environments, representing lagoonal and tidal flat conditions, prevailed at the wellsite during much of the deposition recorded by the Callovian-Bathonian age Iroquois Formation. These environments gave way to a carbonate platform, which formed part of the > 5,000 km long Bahama-Grand Banks gigaplatform that lasted through the end of the Late Jurassic (encompassing the uppermost portion of the Iroquois Formation and the Scatarie Limestone and Bacarro Limestone Members of the Abenaki Formation). The absence of a skeletal-reef association and the dominance of muddy limestone fabrics are evidence that the 145-1 wellsite was located on the platform interior. Major periods of siticiclastic deposition interrupted carbonate deposition, and they are recorded by stratigraphic equivalents of the Mohican Formation, Misaine Shale Member of the Abenaki Formation, and the Mohawk and Mic Mac Formations. A series of sustained prograding delta systems, the earliest of which is preserved as the Missisauga Formation, buried the carbonate platform following its drowning in the Early Cretaceous (Berriasian-Valanginian). The sparser, primarily allochthonous lignite content and better-sorted, glauconite-bearing sands of the Missisauga strata at the 145-1 wellsite suggest that shallow marine or barrier-bar environments were more prevalent than the low delta-plain facies recorded farther shoreward at the COST G-1 wellsite.

Sedimentary Geology↗

USGS2018

Climate stability in Central Anatolia during the Messinian Salinity Crisis

Deposition of large amounts of evaporites and erosion of deep canyons within the Mediterranean Basin as a result of reduced basin connectivity with the Atlantic Ocean and the epicontinental Paratethys Sea characterized the Messinian Salinity Crisis (MSC, 5.97–5.33 Ma). The influence of the MSC on Mediterranean environmental conditions within the basin itself has been intensely studied from marine records, but reconstructing the impact of the MSC on circum-Mediterranean continental climate has been hampered by the absence of continuous sedimentary archives that span the duration of the event. Here, we report results of a continental record of carbon (δ 13 C) and oxygen (δ 18 O) isotopes from lake carbonates framed by new magnetostratigraphic and 40 Ar/ 39 Ar dating, as well as by existing mammal stratigraphy (Kangal Basin, central Anatolia). The sampled section records continuous fluvio-lacustrine sedimentation from ~6.6 Ma to 4.9 Ma, which spans the MSC and the Miocene-Pliocene boundary. This dataset so far represents the only continuous continental paleoenvironmental record of the MSC in the circum-Mediterranean realm. The Kangal Basin isotope record indicates a low degree of evaporation. Furthermore, covariance between δ 13 C and δ 18 O suggests a coupling between lake water balance and biologic productivity. Variations in δ 13 C and δ 18 O therefore likely reflect changes in the amount of incoming precipitation, rather than changes in δ 18 O values of incoming precipitation. The most prominent spike in δ 13 C and δ 18 O occurs during the acme of the MSC and is therefore interpreted to have resulted from a decrease in the amount of incoming moisture correlative to a period of vigorous erosion and sea level lowering in the Mediterranean Basin. Major sea level lowering of Mediterranean basin waters during the acme of the MSC could have therefore led to slightly dryer conditions over Anatolia, which is also suggested by modeling studies. Overall, changes in δ 13 C and δ 18 O values are small. Therefore, we surmise that the MSC had limited effects on the paleoenvironmental and paleoclimatic conditions in the Anatolian interior.

Palaeogeography, Palaeoclimatology, Palaeoecology↗

USGS2001

Sources of salinity near a coal mine spoil pile, north-central Colorado

A small (1 km 2 ) salt-affected stream drainage on the High Plains north of Denver, Colorado was sampled to determine the near-surface dispersion of soluble salts and metals from low-sulfur coal mining waste (spoil). Surface waters collected along the 0.8-km stream reach, and aqueous leachates of spoil and naturally saline local soil, were analyzed for chemical constituents and sulfur isotopes. In this semiarid setting with abundant carbonate-bearing surficial sediments, the limited, mildly acidic drainage from the spoil pile is quickly neutralized, restricting the mobility of many elements. However, some spoil-derived constituents were clearly traceable within the upper 0.4 km of the stream reach. Spoil leachates and surface water near the spoil pile have distinctive compositions of major anions and cations, and elevated levels of dissolved nitrate compared with downstream waters. Spoil-derived sulfate was traceable because it has generally positive values of δ 34 S that contrasted with generally negative values of δ 34 S in soil leachates and evaporite salts from the surrounding area. Spatial–chemical sampling of surface water showed an abrupt increase in dissolved U, Se, B, Li, and Mn in the lower 0.4 km of the stream reach where shallow ground water from surrounding irrigated fields contributed to surface flow. The downstream evolution of surface water chemistry and sulfur isotopic composition is consistent with mixing between spoil-affected upstream water and irrigation-return water. The methods described should be applicable at other sites in similar settings where the environmental effect of low-sulfur coal mining waste must be assessed and where access to samples of shallow ground water is limited.

Colorado↗

USGS1993

The U. S. Geological Survey, Digital Spectral Library: Version 1 (0.2 to 3.0um)

We have developed a digital reflectance spectral library, with management and spectral analysis software. The library includes 498 spectra of 444 samples (some samples include a series of grain sizes) measured from approximately 0.2 to 3.0 um . The spectral resolution (Full Width Half Maximum) of the reflectance data is <= 4 nm in the visible (0.2-0.8 um) and <= 10 nm in the NIR (0.8-2.35 um). All spectra were corrected to absolute reflectance using an NIST Halon standard. Library management software lets users search on parameters (e.g. chemical formulae, chemical analyses, purity of samples, mineral groups, etc.) as well as spectral features. Minerals from borate, carbonate, chloride, element, halide, hydroxide, nitrate, oxide, phosphate, sulfate, sulfide, sulfosalt, and the silicate (cyclosilicate, inosilicate, nesosilicate, phyllosilicate, sorosilicate, and tectosilicate) classes are represented. X-Ray and chemical analyses are tabulated for many of the entries, and all samples have been evaluated for spectral purity. The library also contains end and intermediate members for the olivine, garnet, scapolite, montmorillonite, muscovite, jarosite, and alunite solid-solution series. We have included representative spectra of H2O ice, kerogen, ammonium-bearing minerals, rare-earth oxides, desert varnish coatings, kaolinite crystallinity series, kaolinite-smectite series, zeolite series, and an extensive evaporite series. Because of the importance of vegetation to climate-change studies we have include 17 spectra of tree leaves, bushes, and grasses. The library and software are available as a series of U.S.G.S. Open File reports. PC user software is available to convert the binary data to ascii files (a separate U.S.G.S. open file report). Additionally, a binary data files are on line at the U.S.G.S. in Denver for anonymous ftp to users on the Internet. The library search software enables a user to search on documentation parameters as well as spectral features. The analysis system includes general spectral analysis routines, plotting packages, radiative transfer software for computing intimate mixtures, routines to derive optical constants from reflectance spectra, tools to analyze spectral features, and the capability to access imaging spectrometer data cubes for spectral analysis. Users may build customized libraries (at specific wavelengths and spectral resolution) for their own instruments using the library software. We are currently extending spectral coverage to 150 um. The libraries (original and convolved) will be made available in the future on a CD-ROM.

Open-File Report↗

USGS2015

Geology and hydrocarbon potential of the Dead Sea Rift Basins of Israel and Jordan

Following its middle Miocene inception, numerous basins of varying lengths and depths developed along the Dead Sea fault zone, a large continental transform plate boundary. The modern day left-lateral fault zone has an accumulated left-lateral offset of 105 to 110 km (65 to 68 mi). The deepest basin along the fault zone, the Lake Lisan or Dead Sea basin, reaches depths of 7.5 to 8.5 km (24,500 ft to 28,000 ft), and shows evidence of hydrocarbons. The basins are compartmentalized by normal faulting associated with rapid basin subsidence and, where present, domal uplift accompanying synrift salt withdrawal. The stratigraphy of the fault zone is composed of a thick pre-wrench interval of early Tertiary to Precambrian strata overlain by a syn-wrench section of Miocene to Recent sediments. The main potential source rock is the pre-wrench Cretaceous Maastrichtian Ghareb Formation (and equivalents), which has a total organic carbon (TOC) content measurement of 8 to 18%. Lesser potential source rocks may also be found in the Pleistocene, Cretaceous (Turonian), Jurassic (Oxfordian–Callovian), and Triassic (Ladinian–Carnian). Geochemical analyses indicate that the source of all oils, asphalts, and tars recovered in the Lake Lisan basin is the Ghareb Formation. Geothermal gradients along the Dead Sea fault zone vary from basin to basin. Syn-wrench potential reservoir rocks are highly porous and permeable, whereas pre-wrench strata commonly exhibit lower porosity and permeability. Biogenic gas has been produced from Pleistocene reservoirs. Potential sealing intervals may be present in Neogene evaporites and tight lacustrine limestones and shales. Simple structural traps are not evident; however, subsalt traps may exist. Unconventional source rock reservoir potential has not been tested.

GCSSEPM Foundation Perkins-Rosen Research Conferen↗

USGS2001

The Sirte Basin province of Libya; Sirte-Zelten total petroleum system

The Sirte (Sirt) Basin province ranks 13th among the world?s petroleum provinces, having known reserves of 43.1 bil-lion barrels of oil equivalent (36.7 billion barrels of oil, 37.7 tril-lion cubic feet of gas, 0.1 billion barrels of natural gas liquids). It includes an area about the size of the Williston Basin of the north-ern United States and southern Canada (?490,000 square kilome-ters). The province contains one dominant total petroleum system, the Sirte-Zelten, based on geochemical data. The Upper Cretaceous Sirte Shale is the primary hydrocarbon source bed. Reservoirs range in rock type and age from fractured Precam-brian basement, clastic reservoirs in the Cambrian-Ordovician Gargaf sandstones, and Lower Cretaceous Nubian (Sarir) Sand-stone to Paleocene Zelten Formation and Eocene carbonates commonly in the form of bioherms. More than 23 large oil fields (>100 million barrels of oil equivalent) and 16 giant oil fields (>500 million barrels of oil equivalent) occur in the province. Abstract 1 Production from both clastic and carbonate onshore reservoirs is associated with well-defined horst blocks related to a triple junc-tion with three arms?an eastern Sarir arm, a northern Sirte arm, and a southwestern Tibesti arm. Stratigraphic traps in combina-tion with these horsts in the Sarir arm are shown as giant fields (for example, Messla and Sarir fields in the southeastern portion of the province). Significant potential is identified in areas marginal to the horsts, in the deeper grabens and in the offshore area. Four assessment units are defined in the Sirte Basin prov-ince, two reflecting established clastic and carbonate reservoir areas and two defined as hypothetical units. Of the latter, one is offshore in water depths greater than 200 meters, and the other is onshore where clastic units, mainly of Mesozoic age, may be res-ervoirs for laterally migrating hydrocarbons that were generated in the deep-graben areas. The Sirte Basin reflects significant rifting in the Early Cre-taceous and syn-rift sedimentary filling during Cretaceous through Eocene time, and post-rift deposition in the Oligocene and Miocene. Multiple reservoirs are charged largely by verti-cally migrating hydrocarbons along horst block faults from Upper Cretaceous source rocks that occupy structurally low posi-tions in the grabens. Evaporites in the middle Eocene, mostly post-rift, provide an excellent seal for the Sirte-Zelten hydrocarbon system. The offshore part of the Sirte Basin is complex, with subduction occurring to the northeast of the province boundary, which is drawn at the 2,000-meter isobath. Possible petroleum systems may be present in the deep offshore grabens on the Sirte Rise such as those involving Silurian and Eocene rocks; however, potential of these systems remains speculative and was not assessed.

Bulletin↗

USGS2002

Lithostratigraphic, conodont, and other faunal links between lower Paleozoic strata in northern and central Alaska and northeastern Russia

Lower Paleozoic platform carbonate strata in northern Alaska (parts of the Arctic Alaska, York, and Seward terranes; herein called the North Alaska carbonate platform) and central Alaska (Farewell terrane) share distinctive lithologic and faunal features, and may have formed on a single continental fragment situated between Siberia and Laurentia. Sedimentary successions in northern and central Alaska overlie Late Proterozoic metamorphosed basement; contain Late Proterozoic ooid-rich dolostones, Middle Cambrian outer shelf deposits, and Ordovician, Silurian, and Devonian shallow-water platform facies, and include fossils of both Siberian and Laurentian biotic provinces. The presence in the Alaskan terranes of Siberian forms not seen in wellstudied cratonal margin sequences of western Laurentia implies that the Alaskan rocks were not attached to Laurentia during the early Paleozoic. The Siberian cratonal succession includes Archean basement, Ordovician shallow-water siliciclastic rocks, and Upper Silurian–Devonian evaporites, none of which have counterparts in the Alaskan successions, and contains only a few of the Laurentian conodonts that occur in Alaska. Thus we conclude that the lower Paleozoic platform successions of northern and central Alaska were not part of the Siberian craton during their deposition, but may have formed on a crustal fragment rifted away from Siberia during the Late Proterozoic. The Alaskan strata have more similarities to coeval rocks in some peri-Siberian terranes of northeastern Russia (Kotelny, Chukotka, and Omulevka). Lithologic ties between northern Alaska, the Farewell terrane, and the peri-Siberian terranes diminish after the Middle Devonian, but Siberian afµnities in northern and central Alaskan biotas persist into the late Paleozoic.

Alaska↗

USGS2007

Chapter 3: Geologic Assessment of Undiscovered Oil and Gas Resources in the Phosphoria Total Petroleum System of the Wind River Basin Province, Wyoming

The Phosphoria Total Petroleum System (TPS) encompasses the entire Wind River Basin Province, an area of 4.7 million acres in central Wyoming. The source rocks most likely are black, organic-rich shales of the Meade Peak and Retort Phosphatic Shale Members of the Permian Phosphoria Formation located in the Wyoming and Idaho thrust belt to the west and southwest of the province. Petroleum was generated and expelled during Jurassic and Cretaceous time in westernmost Wyoming and is interpreted to have migrated into the province through carrier beds of the Pennsylvanian Tensleep Sandstone where it was preserved in hypothesized regional stratigraphic traps in the Tensleep and Permian Park City Formation. Secondary migration occurred during the development of structural traps associated with the Laramide orogeny. The main reservoirs are in the Tensleep Sandstone and Park City Formation and minor reservoirs are in the Mississippian Madison Limestone, Mississippian-Pennsylvanian Amsden Formation, Triassic Chugwater Group, and Jurassic Nugget Sandstone and Sundance Formation. The traps are sealed by shale or evaporite beds of the Park City, Amsden, and Triassic Dinwoody Formations, Triassic Chugwater Group, and Jurassic Gypsum Spring Formation. A single conventional oil and gas assessment unit (AU), the Tensleep-Park City AU, was defined for the Phosphoria TPS. Both the AU and TPS cover the entire Wind River Basin Province. Oil is produced from 18 anticlinal fields, the last of which was discovered in 1957, and the possibility of discovering new structural oil accumulations is considered to be relatively low. Nonassociated gas is produced from only two fields, but may be underexplored in the province. The discovery of new gas is more promising, but will be from deep structures. The bulk of new oil and gas accumulations is dependent on the discovery of hypothesized stratigraphic traps in isolated carbonate reservoirs of the Park City Formation. Mean resource estimates for the Tensleep-Park City Conventional Oil and Gas AU total 18 million barrels of oil, 294 billion cubic feet of gas, and 5.9 million barrels of natural gas liquids.

Data Series↗

USGS2016

Aptian ‘Shale Gas’ Prospectivity in the Downdip Mississippi Interior Salt Basin, Gulf Coast, USA

This study evaluates regional ‘shale gas’ prospectivity of the Aptian section (primarily Pine Island Shale) in the downdip Mississippi Salt Basin (MSB). Previous work by the U.S. Geological Survey estimated a mean undiscovered gas resource of 8.8 trillion cubic feet (TCF) in the chronostratigraphic-equivalent Pearsall Formation in the Maverick Basin of south Texas, where industry has established a moderately successful horizontal gas and liquids play. Wells penetrating the downdip MSB Aptian section at depths of 12,000-15,000 ft were used to correlate formation tops in a 15-well cross-section extending about 200 miles (mi) east-southeastward from Adams Co. to Jackson Co. Legacy cuttings from these wells were analyzed for thermal maturity and source rock quality. Bitumen reflectance (n=53) increases with increasing present-day burial depth in the east-central study area from 1.0% to 1.7%. As the Aptian section shallows in Adams Co. to the west, bitumen Ro values are higher (1.7-2.0%), either from relatively greater heat flux or greater mid-Cenomanian uplift and erosion in this area. Total organic carbon (TOC) content ranges 0.01-1.21 and averages 0.5 wt.% (n=51); pyrolysis output (S2; n=51) averages 0.40 mg HC/g rock, indicating little present-day hydrocarbon-generative potential. Bitumen reflectance is preferred as a thermal maturity parameter as Tmax values are unreliable. Normalized X-ray diffraction (XRD) mineral analyses (n=26) indicate high average clay abundance (53 wt.%) relative to quartz (29%) and carbonate (18%). Mineral content shows a spatial relationship to an Appalachian orogen clastic sediment source, with proximal high clay and quartz and distal high carbonate content. Clastic influx from the Appalachian orogen is confirmed by detrital zircon U-Pb ages with dominant Grenville and Paleozoic components [105 ages from a Rodessa sandstone and 112 ages from a Paluxy (Albian) sandstone]. Preliminary information from fluid inclusion microthermometry (41 aqueous measurements from calcite cements in one argillaceous James Limestone sample) indicates homogenization temperatures (Th) of 120-135°C, consistent with present-day bottom-hole conditions and measured bitumen Ro values towards the western end of the MSB. Downdip in the central MSB, microthermometry (26 aqueous measurements from quartz dust rims in one Paluxy sandstone sample) and measured bitumen Ro values indicate maximum temperatures may have been significantly higher (~25°C) than present-day conditions. High inclusion salinities (15-25 wt.% salt) at both locations suggest interaction of pore fluids with evaporites. Mercury injection capillary pressure (MICP) analyses (n=3) indicate porosity ranges 1.3-2.1% and permeability 0.006-0.02 µD for Pine Island and Rodessa shales. Overall, results from this work indicate generally poor ‘shale gas’ prospectivity compared to other shale reservoirs based primarily on depth, low organic content, low porosity, and high clay content. However, thickness and thermal maturity are appropriate, moderate reservoir pressures are present, and petroleum systems modelling by others has indicated high undiscovered gas potential for the basin as a whole.

Conference Paper↗

USGS1981

A process-sedimentary framework for characterizing recent and ancient sabkhas

The discovery of sabkha environments during the 1960's, marked the beginning of Recent evaporite sedimentological studies and their perception as models for facies analysis. However, variation among Recent sabkhas, though recognized by the geologic community, has not been duly addressed, which has resulted in overuse of the Trucial Coast model in comparative sedimentological studies. Knowledge of the dominant physical processes which determine sabkha morphology, and of the sedimentary response to those processes, can lead to a fundamental understanding of a sabkha's origin and of how it differs from other sabkhas. Physical processes thought to be most important (besides evaporation) include those operative under: (1) marine-; (2) fluvial-lacustrine-; and (3) eolian-dominated conditions. Dominance of one or more of these in the proper settings give rise to marine coastal sabkhas, continental playas, and interdune sabkhas. Sedimentary responses to dominant physical processes lead to the development of sabkhas consisting of a combination of either: (1) terrigenous clastics; (2) carbonate-sulfate (anhydrite-gypsum) minerals; or (3) soluble salts (halite, sylvite, polyhalite, etc.). Sediment characterization can also allow discrimination of the range or compositional variety in, for example, coastal sabkhas. Where applied to the stratigraphic record, this classification system may help unravel the sedimentary history of an ancient sabkha system, and a determination of the dominant physical processes that ruled its development.

Sedimentary Geology↗

USGS2006

Unusual Holocene and late Pleistocene carbonate sedimentation in Bear Lake, Utah and Idaho, USA

Bear Lake (Utah-Idaho, USA) has been producing large quantities of carbonate minerals of varying mineralogy for the past 17,000 years. The history of sedimentation in Bear Lake is documented through the study of isotopic ratios of oxygen, carbon, and strontium, percent organic carbon, percent CaCO3, X-ray diffraction mineralogy, HCl-leach inorganic geochemistry, and magnetic properties on samples from three piston cores. Historically, the Bear River, the main source of water for Great Salt Lake, did not enter Bear Lake until it was artificially diverted into the lake at the beginning of the 20th century. However, during the last glacial interval, the Bear River did enter Bear Lake depositing red, calcareous, silty clay. About 18,000 years ago, the Bear River became disconnected from Bear Lake. A combination of warmer water, increased evaporation, and increased organic productivity triggered the precipitation of calcium carbonate, first as calcite. As the salinity of the lake increased due to evaporation, aragonite began to precipitate about 11,000 years ago. Aragonite is the dominant mineral that accumulated in bottom sediments of the lake during the Holocene, comprising an average of about 70 wt.% of the sediments. Aragonite formation in a large, cold, oligotrophic, high latitude lake is highly unusual. Lacustrine aragonite usually is found in small, saline lakes in which the salinity varies considerably over time. However, Bear Lake contains endemic ostracodes and fish, which indicate that the chemistry of the lake has remained fairly constant for a long time. Stable isotope data from Holocene aragonite show that the salinity of Bear Lake increased throughout the Holocene, but never reached highly evolved values of ??18O in spite of an evaporation-dominated water balance. Bear Lake hydrology combined with evaporation created an unusual situation that produced large amounts of aragonite, but no evaporite minerals.

Sedimentary Geology↗

USGS1970

Mineral resources of the southern half of Zone III Santander, Norte de Santander and Boyaca, Colombia

The areas covered by this report lies in the eastern Cordillera of the Colombian Andes in the region around Bucaramanga. This part of the eastern Cordillera consists of a structurally complex core of metamorphic and igneous rocks of Precambrian to Mesozoic age, flanked to east and west by faulted and folded sedimentary strata of late Paleozoic to Tertiary age. Infaulted blocks of sedimentary rocks are locally present in the massif. Unconsolidated deposits of Quaternary age, primarily terraced alluvium, are 10cally extensive in valleys on the flanks of the range. The crystalline central core of the range is called the Santander massif. In it are located the principal sold deposits and scattered deposits of copper, lead, zinc, and fluorite. The sedimentary rocks flanking the massif contain significant deposits of phosphate rock and gypsum, as well as other nonmetallic industrial minerals such as limestone, barite, glass sand, and coal. A belt of lead-zinc prospects in carbonate and sandstone beds of Cretaceous age on the east side of the range warrants further investigation. Gold and silver are the only important metallic minerals that have been produced in the Santander massif. Mining dates back to colonial and possibly to pre-colonial times and continues on a small scale at present. The California and Vetas district was the main area of investigation of metallic minerals during the present project. Results of geochemical sampling of stream sediments and assays of vein material indicate that the main potential of the area is in gold with lesser potentials in copper, lead, zinc, and silver. Mineralization of the district is probably younger than Early Cretaceous. Although no copper minerals have been mined elsewhere in the massif, small amounts of copper minerals in various rocks in scattered areas is revealed by green and blue stains of copper carbonates and sulfates. Deposits of greatest areal extent are in arkosic conglomeratic beds of the Giron Formation. These are being explored and sampled at the present time (1969). A little lead has been mined and smelted in the past but operations were on a very small scale and of short duration. Small amounts of lead, zinc, and copper minerals accompany dolomite replacement of Cretaceous limestone in a few scattered places, and several promising prospects are being investigated by means of trenches and drilling. One magnetite and several hematite prospects were examined but none offers any potential for economic development. Thick beds of gypsum in Lower Cretaceous limestone on Mesa de Los Santos, south of Bucaramanga are being quarried from outcrops for use in cement manufacture. The deposit was discovered shortly before the present project began, and although its extent beneath overlying strata is not yet determined by drilling, it appears to be in a small evaporite basin of about three kilometers in radius. Reserves of gypsum are large, but future development will have to be by underground mining. Outcrops of Cretaceous limestone of high purity are widespread and are more than adequate to meet all demands, which at present are for cement and calcined lime, road construction material, and to a small extent for agricultural lime and polished decorative stone. Upper Paleozoic limestone of the Diamante Formation crops out in a few places; it has been used near Bucaramanga for cement manufacture. Marble is present in several localities of the Santander massif in Lower Paleozoic and Devonian rocks. Impurities, fractures, and solution cavities render most of it unsuitable for decorative purposes, but selected parts are used in floor tile and terrazo. Recrystallized limestone of the Diamante Formation in the same area, usually referred to as marble, is of uniform high purity throughout a thick and uninterrupted section, and offers a good source of limestone raw material. A little is now used for agricultural lime. The potential of this resource has not been fully evalua

Open-File Report↗

USGS2015

Extreme variation of sulfur isotopic compositions in pyrite from the Qiuling sediment-hosted gold deposit, West Qinling orogen, central China: An in situ SIMS study with implications for the source of sulfur

High spatial resolution textural (scanning electron microscope (SEM)), chemical (electron microprobe (EMP)) and laser ablation-inductively coupled plasma-mass spec- trometry (LA-ICP-MS)), and sulfur isotopic (secondary ion mass spectrometry (SIMS)) analyses of pyrite from the Qiuling sediment-hosted gold deposit (232±4 Ma) in the West Qinling orogen, central China were conducted to distinguish pyrite types and gain insights into the source and evolution of sulfur in hydrothermal fluids. The results reveal an enormous variation (−27.1 to +69.6‰) in sulfur isotopic composition of pyrite deposited during three paragenetic stages. Pre-ore framboidal pyrite, which is characterized by low concentra- tions of As, Au, Cu, Co, and Ni, has negative δ34S values of −27.1 to −7.6‰ that are interpreted in terms of bacterial re- duction of marine sulfate during sedimentation and diagenesis of the Paleozoic carbonate and clastic sequences, the predom- inant lithologies in the deposit area, and the most important hosts of many sediment-hosted gold deposits throughout the West Qinling orogen. The ore-stage hydrothermal pyrite con- tains high concentrations of Au, As, Cu, Sb, Tl, and Bi and hasa relatively narrow range of positive δ34S values ranging from +8.1 to +15.2‰. The sulfur isotope data are comparable to those of ore pyrite from many Triassic orogenic gold deposits and Paleozoic sedimentary exhalative (SEDEX) Pb-Zn de- posits in the West Qinling orogen, both being hosted mainly in the Devonian sequence. This similarity indicates that sulfur, responsible for the auriferous pyrite at Qiuling, was largely derived from the metamorphic devolatization of Paleozoic marine sedimentary rocks. Post-ore-stage pyrite, which is sig- nificantly enriched in Co and Ni but depleted in Au and As, has unusually high δ34S values ranging from +37.4 to +69.6 ‰, that are interpreted to result from thermochemical reduc- tion of evaporite sulfates in underlying Cambrian sedimentary rocks with very high δ34S values. The variations in Au content and sulfur isotopic compositions across a single ore-stage py- rite grain may reflect displacement of indigenous groundwater with low δ34S values by auriferous metamorphic fluids with high δ34S values. The very low-grade metamorphism of the host rocks and the metamorphic derivation of sulfur for the ore pyrite indicate that the Qiuling sediment-hosted gold deposit is an epizonal manifestation of an orogenic gold system in the West Qinling orogen.

Mineralium Deposita↗

USGS2004

Numerical analysis of seawater circulation in carbonate platforms: II. The dynamic interaction between geothermal and brine reflux circulation

Density-driven seawater circulation may occur in carbonate platforms due to geothermal heating and / or reflux of water of elevated salinity. In geothermal circulation lateral contrasts in temperature between seawater and platform groundwaters warmed by the geothermal heat flux result in upward convective flow, with colder seawater drawn into the platform at depth. With reflux circulation, platform-top waters concentrated by evaporation flow downward, displacing less dense underlying groundwaters. We have used a variable density groundwater flow model to examine the pattern, magnitude and interaction of these two different circulation mechanisms, for mesosaline platform-top waters ( 50 ‰ ) and brines concentrated up to saturation with respect to gypsum ( 150 ‰ ) and halite ( 246 ‰ ). Geothermal circulation, most active around the platform margin, becomes restricted and eventually shut-off by reflux of brines from the platform interior towards the margin. The persistence of geothermal circulation is dependent on the rate of brine reflux, which is proportional to the concentration of platform-top brines and also critically dependent on the magnitude and distribution of permeability. Low permeability evaporites can severely restrict reflux whereas high permeability units in hydraulic continuity enhance brine transport. Reduction in permeability with depth and anisotropy of permeability (kv < < kh) focuses flow laterally in the shallow subsurface (<1 km), resulting in a horizontally elongated brine plume. Aquifer porosity and dispersivity are relatively minor controls on reflux. Platform brines can entrain surficial seawater when brine generating conditions cease but the platform-top remains submerged, a variant of reflux we term "latent reflux". Brines concentrated up to gypsum saturation have relatively long residence times of at least 100 times the duration of the reflux event. They thus represent a long-term control on post-reflux groundwater circulation, and consequently on the rates and spatial patterns of shallow burial diagenesis, such as dolomitization.

American Journal of Science↗

USGS2002

The major-ion composition of Silurian seawater

One-hundred fluid inclusions in Silurian marine halite were analyzed in order to determine the major-ion composition of Silurian seawater. The samples analyzed were from three formations in the Late Silurian Michigan Basin, the A-1, A-2, and B Evaporites of the Salina Group, and one formation in the Early Silurian Canning Basin (Australia), the Mallowa Salt of the Carribuddy Group. The results indicate that the major-ion composition of Silurian seawater was not the same as present-day seawater. The Silurian ocean had lower concentrations of Mg2+, Na+, and SO2-4, and much higher concentrations of Ca2+ relative to the ocean's present-day composition. Furthermore, Silurian seawater had Ca2+ in excess of SO2-4. Evaporation of Silurian seawater of the composition determined in this study produces KC1-type potash minerals that lack the MgSO4-type late stage salts formed during the evaporation of present-day seawater. The relatively low Na+ concentrations in Silurian seawater support the hypothesis that oscillations in the major-ion composition of the oceans are primarily controlled by changes in the flux of mid-ocean ridge brine and riverine inputs and not global or basin-scale, seawater-driven dolomitization. The Mg2+/Ca2+ ratio of Silurian seawater was ~1.4, and the K+/Ca2+ ratio was ~0.3, both of which differ from the present-day counterparts of 5 and 1, respectively. Seawaters with Mg2+/Ca2+ <2 facilitate the precipitation of low-magnesian calcite (mol % Mg < 4) marine ooids and submarine carbonate cements whereas seawater with Mg2+/Ca2+ >2 (e.g., modern seawater) facilitate the precipitation of aragonite and high-magnesian calcite. Therefore, the early Paleozoic calcite seas were likely due to the low Mg2+/Ca2+ ratio of seawater, not the pCO2 of the Silurian atmosphere. Copyright ?? 2002 Elsevier Science Ltd.

Geochimica et Cosmochimica Acta↗

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↗