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At least 163 records · Page 9Linked to original sources

Report of the committee on chemistry of natural waters, 1936–37

The membership of this Committee is as follows: C. S. Howard, Chairman, U. S. Geological Survey, Washington, D.C. D. G. Thompson, U. S. Geological Survey, Washington, D.C. A. C. Lane, 22 Arlington Street, Cambridge, Massachusetts C. S. Scofield, Bureau of Plant Industry, U. S. Dept. Agri., Washington, D. C. I. A. Denison, U.S. Bureau of Standards, Washington, D.C. T. G. Thompson, University of Washington, Seattle, Washington W. P. Kelley, Citrus Experiment Station, Riverside, California In order to provide for close cooperation between the work of the different research‐committees of the American Geophysical Union it was decided to have the chairmen of certain committees serve on other committees. The Chairman of the Committee on the Chemistry of Natural Waters is serving on the Committee of Underground waters and D. G. Thompson as Chairman of the Committee on Underground Waters is serving on the Committee on Chemistry of Natural Waters

Eos, Transactions, American Geophysical Union↗

Nanoscale silicate melt textures determine volcanic ash surface chemistry

Explosive volcanic eruptions produce vast quantities of silicate ash, whose surfaces are subsequently altered during atmospheric transit. These altered surfaces mediate environmental interactions, including atmospheric ice nucleation, and toxic effects in biota. A lack of knowledge of the initial, pre-altered ash surface has required previous studies to assume that the ash surface composition created during magmatic fragmentation is equivalent to the bulk particle assemblage. Here we examine ash particles generated by controlled fragmentation of andesite and find that fragmentation generates ash particles with substantial differences in surface chemistry. We attribute this disparity to observations of nanoscale melt heterogeneities, in which Fe-rich nanophases in the magmatic melt deflect and blunt fractures, thereby focusing fracture propagation within aureoles of single-phase melt formed during diffusion-limited growth of crystals. In this manner, we argue that commonly observed pre-eruptive microtextures caused by disequilibrium crystallisation and/or melt unmixing can modify fracture propagation and generate primary discrepancies in ash surface chemistry, an essential consideration for understanding the cascading consequences of reactive ash surfaces in various environments.

Nature Communications↗

Long-term trends in Arctic riverine chemistry signal multi-faceted northern change

Rivers integrate processes occurring throughout their watersheds and are therefore sentinels of change across broad spatial scales. River chemistry also regulates ecosystem function across Earth’s land–ocean continuum, exerting control from the micro- (for example, local food web) to the macro- (for example, global carbon cycle) scale. In the rapidly warming Arctic, a wide range of processes—from permafrost thaw to biological uptake and transformation—might reasonably alter river water chemistry. Here we use data from major rivers that collectively drain two-thirds of the Arctic Ocean watershed to assess widespread change in biogeochemical function within the pan-Arctic basin from 2003 to 2019. While the oceanward flux of alkalinity and associated ions increased markedly over this time frame, nitrate and other inorganic nutrient fluxes declined. Fluxes of dissolved organic carbon showed no overall trend. This divergence in response indicates the perturbation of multiple processes on land, with implications for biogeochemical cycling in the coastal ocean. We anticipate that these findings will facilitate refinement of conceptual and numerical models of current and future functioning of Arctic coastal ecosystems and spur research on scale-dependent change across the river-integrated Arctic domain.

Arctic↗

Fines classification based on sensitivity to pore-fluid chemistry

The 75-μm particle size is used to discriminate between fine and coarse grains. Further analysis of fine grains is typically based on the plasticity chart. Whereas pore-fluid-chemistry-dependent soil response is a salient and distinguishing characteristic of fine grains, pore-fluid chemistry is not addressed in current classification systems. Liquid limits obtained with electrically contrasting pore fluids (deionized water, 2-M NaCl brine, and kerosene) are combined to define the soil “electrical sensitivity.” Liquid limit and electrical sensitivity can be effectively used to classify fine grains according to their fluid-soil response into no-, low-, intermediate-, or high-plasticity fine grains of low, intermediate, or high electrical sensitivity. The proposed methodology benefits from the accumulated experience with liquid limit in the field and addresses the needs of a broader range of geotechnical engineering problems.

Journal of Geotechnical and Geoenvironmental Engin↗

Network analysis reveals multiscale controls on streamwater chemistry

By coupling synoptic data from a basin-wide assessment of streamwater chemistry with network-based geostatistical analysis, we show that spatial processes differentially affect biogeochemical condition and pattern across a headwater stream network. We analyzed a high-resolution dataset consisting of 664 water samples collected every 100 m throughout 32 tributaries in an entire fifth-order stream network. These samples were analyzed for an exhaustive suite of chemical constituents. The fine grain and broad extent of this study design allowed us to quantify spatial patterns over a range of scales by using empirical semivariograms that explicitly incorporated network topology. Here, we show that spatial structure, as determined by the characteristic shape of the semivariograms, differed both among chemical constituents and by spatial relationship (flow-connected, flow-unconnected, or Euclidean). Spatial structure was apparent at either a single scale or at multiple nested scales, suggesting separate processes operating simultaneously within the stream network and surrounding terrestrial landscape. Expected patterns of spatial dependence for flow-connected relationships (e.g., increasing homogeneity with downstream distance) occurred for some chemical constituents (e.g., dissolved organic carbon, sulfate, and aluminum) but not for others (e.g., nitrate, sodium). By comparing semivariograms for the different chemical constituents and spatial relationships, we were able to separate effects on streamwater chemistry of (i) fine-scale versus broad-scale processes and (ii) in-stream processes versus landscape controls. These findings provide insight on the hierarchical scaling of local, longitudinal, and landscape processes that drive biogeochemical patterns in stream networks.

Proceedings of the National Academy of Sciences↗

Effects of depletion sampling by standard three-pass pulsed DC electrofishing on blood chemistry parameters of fishes from Appalachian streams

Adverse effects on fishes captured by electrofishing techniques have long been recognized, although the extent of associated physical injury and behavioral alterations are highly variable and dependent on a number of factors. We examined the effects of three-pass pulsed DC (PDC) electrofishing on two salmonid species (Rainbow Trout Oncorhynchus mykiss and Brook Trout Salvelinus fontinalis) and five other genera (Green Sunfish Lepomis cyanellus, Potomac Sculpin Cottus girardi, Fathead Minnow Pimephales promelas, Largemouth Bass Micropterus salmoides, and Channel Catfish Ictalurus punctatus) common to Appalachian streams. We examined the corresponding effects of PDC electroshock on the following physiological indicators of stress and trauma: blood glucose and serum lactate, as well as on other blood chemistry, namely, enzymes, electrolytes, minerals, and proteins. All species demonstrated physiological responses to PDC electroshock, indicated by the biochemical differences in blood parameters in unshocked and shocked groups of fish with or without gross evidence of hemorrhagic trauma. Serum lactate was the most consistent indicator of these effects. Significant differences in whole blood glucose levels were also noted in treatment groups in all species except Green Sunfish, although the patterns observed were not as consistent as for serum lactate. Elevations in the serum enzymes, aspartate aminotransferase and creatine kinase, in the electroshocked fish occurred only in the two salmonid species. In many instances, although blood parameters were elevated in electroshocked fish compared with the unshocked controls for a given species, there were no differences in those levels in electroshocked fish based on the presence of gross hemorrhagic trauma to axial musculature. While some of the blood parameters examined correlated with both the occurrence of electroshock and the resultant tissue injury, there was no apparent link between the altered blood chemistry and increased mortality 30 d after electrofishing.

Appalachian Mountains↗

Temperature, water chemistry, and optical properties of Crater Lake

Water temperature, water chemistry, and optical properties of Crater Lake were studied from 1983 to 1991. In winter and spring, wind energy and convection mixed the water column to a depth of 200 to 250 m. The lake was thermally stratified in summer and early fall; however, the epilimnion was only 5 to 20 m thick, and most of the 589 m deep water column was a cold hypolimnion. The lake was slightly basic, with moderate alkalinity and conductivity. The water column was oxygenated, although slight decreases in dissolved oxygen concentration were noticed near the lake bottom in late summer and early fall. Phosphorus and nitrogen concentrations were low. Orthophosphorus-P concentrations increased slightly with increased lake depth, whereas nitrate-N was below detection limits in the upper 200 m of the water column and then increased with increased lake depth. Secchi disk clarity typically varied from the high-20-m to low-30-m range. The depth of 1 % surface incident light (425–655 nm) in July and August typically ranged between 80 and 100 m. The results also indicated that water temperature, water chemistry, and optical properties of the lake between 1983 and 1991 were consistent with those observed between 1896 and 1982.

Journal of Lake and Reservoir Management↗

Understanding the evolution of groundwater-contaminant plume chemistry emanating from legacy contaminant sources: An example from a long-term crude oil spill

Understanding the evolution of plumes emanating from residual hydrocarbon contaminant sources requires evaluating how changes in source compositions over time cause changes in dissolved plume chemistry as residual sources age. This study investigates such changes at the site of a 1979 crude-oil pipeline spill and is the first comprehensive look at groundwater chemistry associated with a residual hydrocarbon source zones in different stages of aging. The data show a direct relationship between concentrations of benzene and naphthalene in the residual oil and those measured in water samples collected below the oil. Groundwater associated with oil near the spill site had different chemical composition compared with water associated with oil that had spread downgradient from the spill zone, indicating a shift in biodegradation reactions. These results emphasize that source zone processes are spatially and temporally heterogeneous and should be accounted for in natural attenuation studies where residual source zones persist.

Minnesota↗

Water chemistry and its effects on the physiology and survival of Atlantic salmon Salmo salar smolts

The physiological effects of episodic pH fluctuations on Atlantic salmon Salmo salar smolts in eastern Maine, U.S.A., were investigated. During this study, S. salar smolts were exposed to ambient stream‐water chemistry conditions at nine sites in four catchments for 3 and 6 day intervals during the spring S. salar smolt migration period. Plasma chloride, plasma glucose, gill aluminium and gill Na + ‐ and K + ‐ATPase levels in S. salar smolts were assessed in relation to ambient stream‐water chemistry during this migration period. Changes in both plasma chloride and plasma glucose levels of S. salar smolts were strongly correlated with stream pH, and S. salar smolt mortality occurred in one study site with ambient stream pH between 5·6 and 5·8 during the study period. The findings from this study suggest that physiological effects on S. salar smolts are strongly correlated with stream pH and that in rivers and streams with low dissolved organic carbon (DOC) concentrations the threshold for physiological effects and mortality probably occurs at a higher pH and shorter exposure period than in rivers with higher DOC. Additionally, whenever an acidification event in which pH drops below 5·9 coincides with S. salar smolt migration in eastern Maine rivers, there is potential for a significant reduction in plasma ions of S. salar smolts.

Maine↗

Bottled water, spas, and early years of water chemistry

Although hot springs have been used and enjoyed for thousands of years, it was not until the late 1700s that they changed the course of world civilization by being the motivation for development of the science of chemistry. The pioneers of chemistry such as Priestley, Cavendish, Lavoisier, and Henry were working to identify and generate gases, in part, to determine their role in carbonated beverages. In the 18th century, spas in America were developed to follow the traditional activities of popular European spas. However, they were to become a dominant political and economic force in American history on three major points: (1) By far the most important was to provide a place for the leaders of individual colonies to meet and discuss the need for separation from England and the necessity for the Revolutionary War; (2) the westward expansion of the United States was facilitated by the presence of hot springs in many locations that provided the economic justification for railroads and settlement; and (3) the desire for the preservation of hot springs led to the establishment of the National Park Service. Although mineral springs have maintained their therapeutic credibility in many parts of the world, they have not done so in the United States. We suggest that the American decline was prompted by: (1) the establishment of The Johns Hopkins School of Medicine in 1893; (2) enactment of the Pure Food and Drug Act of 1907; and (3) the remarkable achievement of providing safe water supplies for American cities by the end of the 1920s. The current expanding market for bottled water is based in part on bottled water being an alternative beverage Ito alcohol and sweetened drinks and the inconsistent palatability and perceived health hazards of some tap waters.

Groundwater↗

A computer-assisted graphical method for identification and correlation of igneous rock chemistries

We have devised a computer-assisted graphical method for correlating chemical analyses in suites of related igneous rocks. The method provides a direct and empirical means of sample identification using all of the reported chemistry. In a study of basalt of the Columbia River plateau, the method has been used for (1) checking field identifications of rocks, (2) spotting analytical errors in analyses of samples of known chemical type, (3) identifying repetitions of chemistry in thick stratigraphic sections, and (4) matching analyses of dikes to those of flows that the dikes may have fed. Program OXVAR creates a set of oxide-oxide variation diagrams on a CALCOMP plotter; any oxide may be used as the base (for example, MgO, SiO 2 ). For each oxide-oxide variation diagram, program CTSET creates the smallest convex polygon that encloses all the data points as well as a larger polygon that takes into account the error in determination of each data point. A set of nested polygons, one for each oxide, then represents a chemical type. Program CTYPE identifies unknown analyses by comparing them with all defined chemical types. If all the elements or oxides of an analysis plot within the defined polygons for a given chemical type, then an identification is printed. If at least one element of an analysis falls outside the set of polygons defined for each chemical type, then “unidentified” is printed, and qualitative information on the amount of deviation from the defined chemical types is given.

Geology↗

Petrology and chemistry of the Green Acres gabbro complex near Winchester, Riverside County, California

The Cretaceous Green Acres layered igneous complex, northeast of Winchester, California, is composed of a suite of olivine- and hornblende-bearing gabbros in the Peninsular Ranges batholith within the Perris tectonic block. A consistent mineral assemblage is observed throughout the complex, but there is considerable textural and modal heterogeneity. Both preclude a consistent set of principles based on appearance and mineralogy on which to delineate map units. Distinct changes in the chemistry of olivine, pyroxene, and hornblende, however, serve to define discrete mappable units, and the complex has been divided into five geochemical map units on this basis. Limited whole-rock data show the Green Acres complex is chemically comparable to other Peninsular Ranges batholith gabbroic rocks, and rare earth element (REE) concentrations and patterns are typical of magmas generated in convergent margin settings. For the complex as a whole, olivine is Fo 80–35 , plagioclase is An 100–64 , clinopyroxene is Wo 49–41 En 48–38 Fs 18–6 and Wo 36–26 En 65–42 Fs 30–8 , and orthopyroxene is Wo 5–0 En 78–42 Fs 50–21 , where Fo is forsterite, An is anorthite, Wo is wollastonite, En is enstatite, and Fs is ferrosilite. The Mg/(Mg + ΣFe) atomic ratio in hornblende ranges from 0.84 to 0.50. Magmatic lineations and modal and textural layering are prevalent throughout the complex. Mineral chemistry does not change in any systematic way within and between layers in any map unit. Although the strike of layering varies, in any map unit at any given location it is the same in all units irrespective of intrusive order. Thin dikes, typically late-stage hornblende gabbro, commonly intrude parallel to layering. The strikes of magmatic lineations and modal layers are consistent with the populations of strikes of fabrics in the metamorphic basement as well as tectonic features in surrounding, postgabbro granitic rocks. These relations imply that the regional state of stress at the time of gabbro emplacement played a role in layer formation in conjunction with thermal and hydraulic pressure perturbations.

California↗

Of travertine and time: otolith chemistry and microstructure detect provenance and demography of endangered humpback chub in Grand Canyon, USA

We developed a geochemical atlas of the Colorado River in Grand Canyon and in its tributary, the Little Colorado River, and used it to identify provenance and habitat use by Federally Endangered humpback chub, Gila cypha. Carbon stable isotope ratios (δ 13 C) discriminate best between the two rivers, but fine scale analysis in otoliths requires rare, expensive instrumentation. We therefore correlated other tracers (SrSr, Ba, and Se in ratio to Ca) to δ 13 C that are easier to quantify in otoliths with other microchemical techniques. Although the Little Colorado River’s water chemistry varies with major storm events, at base flow or near base flow (conditions occurring 84% of the time in our study) its chemistry differs sufficiently from the mainstem to discriminate one from the other. Additionally, when fish egress from the natal Little Colorado River to the mainstem, they encounter cold water which causes the otolith daily growth increments to decrease in size markedly. Combining otolith growth increment analysis and microchemistry permitted estimation of size and age at first egress; size at first birthday was also estimated. Emigrants < 1 year old averaged 51.2 ± 4.4 (SE) days and 35.5 ± 3.6 mm at egress; older fish that had recruited to the population averaged 100 ± 7.8 days old and 51.0 ± 2.2 mm at egress, suggesting that larger, older emigrants recruit better. Back-calculated size at age 1 was unimodal and large (78.2 ± 3.3 mm) in Little Colorado caught fish but was bimodally distributed in Colorado mainstem caught fish (49.9 ± 3.6 and 79 ± 4.9 mm) suggesting that humpback chub can also rear in the mainstem. The study demonstrates the coupled usage of the two rivers by this fish and highlights the need to consider both rivers when making management decisions for humpback chub recovery.

Arizona↗

Summit crater lake observations, and the location, chemistry, and pH of water samples near Mount Chiginagak volcano, Alaska: 2004-2012

Mount Chiginagak is a hydrothermally active volcano on the Alaska Peninsula, approximately 170 km south–southwest of King Salmon, Alaska (fig. 1). This small stratovolcano, approximately 8 km in diameter, has erupted through Tertiary to Permian sedimentary and igneous rocks (Detterman and others, 1987). The highest peak is at an elevation of 2,135 m, and the upper ~1,000 m of the volcano are covered with snow and ice. Holocene activity consists of debris avalanches, lahars, and lava flows. Pleistocene pyroclastic flows and block-and-ash flows, interlayered with andesitic lava flows, dominate the edifice rocks on the northern and western flanks. Historical reports of activity are limited and generally describe “steaming” and “smoking” (Coats, 1950; Powers, 1958). Proximal tephra collected during recent fieldwork suggests there may have been limited Holocene explosive activity that resulted in localized ash fall. A cluster of fumaroles on the north flank, at an elevation of ~1,750 m, commonly referred to as the “north flank fumarole” have been emitting gas throughout historical time (location shown in fig. 2). The only other thermal feature at the volcano is the Mother Goose hot springs located at the base of the edifice on the northwestern flank in upper Volcano Creek, at an elevation of ~160 m (fig. 2, near sites H1, H3, and H4). Sometime between November 2004 and May 2005, a ~400-m-wide, 100-m-deep lake developed in the snow- and ice-filled summit crater of the volcano (Schaefer and others, 2008). In early May 2005, an estimated 3 million cubic meters (3×106 m3) of sulfurous, clay-rich debris and acidic water exited the crater through tunnels at the base of a glacier that breaches the south crater rim. More than 27 km downstream, these acidic flood waters reached approximately 1.3 m above normal water levels and inundated a fertile, salmon-spawning drainage, acidifying the entire water column of Mother Goose Lake from its surface waters to its maximum depth of 45 m (resulting pH ~2.9), and preventing the annual salmon run in the King Salmon River. A simultaneous release of gas and acidic aerosols from the crater caused widespread vegetation damage along the flow path. Since 2005, we have been monitoring the crater lake water that continues to flow into Mother Goose Lake by collecting surface water samples for major cation and anion analysis, measuring surface-water pH of affected drainages, and photo-documenting the condition of the summit crater lake. This report describes water sampling locations, provides a table of chemistry and pH measurements, and documents the condition of the summit crater between 2004 and 2011. In September 2013, the report was updated with results of water-chemistry samples collected in 2011 and 2012, which were added as an addendum.

Alaska↗

Effects of nonlethal sea lamprey attack on the blood chemistry of lake trout

A laboratory study examined changes in the blood chemistry of field-caught and hatchery-reared lake trout Salvelinus namaycush subjected to a nonlethal attack by sea lampreys Petromyzon marinus. We measured glucose, total protein, amylase, alkaline phosphatase (ALKP), alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatine kinase, calcium, magnesium, triglycerides, sodium, and potassium with a Kodak Ektachem DT60 Analyzer, Ektachem DTSC Module, and the DTE Module. Mean levels of total protein, AST, ALKP, hematocrit, calcium, magnesium, and sodium decreased significantly ( P ≤ 0.05), and mean levels of ALT and potassium increased significantly ( P ≤ 0.05) after sea lamprey feeding. Lake trout condition ( K ) and hematocrit levels also decreased significantly ( P ≤ 0.05) after the sea lamprey attack. Frequency distributions of eight lake trout blood chemistry variables and the hematocrit were significantly different before and after a sea lamprey attack. A second study that used hatchery lake trout broodstock measured changes in hematocrit before and after a sea lamprey attack.

Michigan↗

Reference values and comparison of blood chemistry and plasma protein values between gold standard analyzers and four point-of-care devices in free-ranging canvasbacks (Aythya valisineria)

Accurate, timely, and cost-effective blood chemistry analysis is an essential tool for directing emergency treatment, monitoring the health status of captive and free-ranging individuals and flocks, and improving the efficacy of conservation actions. Blood samples were obtained from 52 canvasbacks ( Aythya valisineria ) that were captured on San Francisco Bay, California, during December 2017 as part of a long-term study. Reference values and clinical agreement were determined for blood chemistry and plasma protein parameters among four commonly used point-of-care devices (VetScan ® VS2, i-STAT ® , AlphaTRAK ® 2 glucometer, refractometer) and two gold standard laboratory analyzers (Roche cobas ® c501, Helena SPIFE 3000 system). Canvasback reference values were generally within expected ranges for Anatidae species with the exception of higher upper limits for sodium and chloride. Creatine kinase and aspartate transaminase values exceeded a published threshold for diagnosis of capture myopathy even though study birds were captured using low-stress techniques and successfully released. With the exception of higher alkaline phosphatase in hatch-year canvasbacks, no age or sex differences were observed for any analyte in this population that was captured during a nonbreeding period. Analysis of analyzer agreement found raw VetScan aspartate transaminase, calcium, glucose, and uric acid values; corrected VetScan albumin, potassium, sodium, and total protein values; raw i-STAT glucose and potassium values; and corrected i-STAT sodium and chloride values were clinically interchangeable with Roche cobas values. Raw VetScan and i-STAT glucose values were also interchangeable. However, none of the Roche or point-of-care analyzer plasma protein values were in clinical agreement with gold standard electrophoresis values. The findings of this study highlight the need for analyzer- or technique-specific reference values and provide biologists and veterinarians quantitative reference values using currently available analyzers to better assess and respond to the health of individuals and populations.

California↗

The chemistry of eolian quartz dust and the origin of chert

Among the numerous models that have been suggested for the primary and predominant source of silica for chert, we suggest that eolian dust is worthy of further considerations. Such considerations are supported by the common association of Phanerozoic chert with evaporites, limestones, dolomites, or other strata that were deposited within or near arid paleoclimates. This association suggests a direct or indirect causal link between aridity and chert formation. In addition, eolian processes export large quantities of quartz-rich dust from arid climate ergs or loess lands. The chemistry of abraded quartz particles derived therefrom is consistent with chert formation. Abrasion of quartz particles produces an amorphous surface layer and underlying lattice disorder. An inverse relation between particle size distribution (< 64 μm) and the enthalpy of solution of abraded quartz is indicative of the degree of lattice disorder; as particle size decreases, the enthalpy of solution increases. The amorphous surface layer and underlying lattice disorder enhance both the rate and amount of dissolution of quartz dust particles; the solubilized silica can then be reprecipitated and diagenetically altered to the various silica polymorphs that occur in chert. An eolian supply and the chemistry of eolian abraded quartz particles may account for chert formation in disparate depositional environments that encompass deep-sea chert, chert in epicontinental seas including shallow shelves, and chert that formed in continental eolinites, lakes, and soils (arid climate silcretes).

Journal of Sedimentary Research↗

Mineralogy, chemistry, and fluid-aided evolution of the Pea Ridge Fe oxide-(Y + REE) deposit, southeast Missouri, USA

The Kiruna-type Pea Ridge iron oxide-apatite (IOA) deposit is hosted by a sequence of 1.47 Ga rhyolite tuffs of the St. Francois Mountains, southeast Missouri, USA. It consists of a series of altered zones composed mainly of amphibole, magnetite, hematite, and quartz, together with the presence of several rare earth element (Y + REE)-rich breccia pipes. In many cases, the fluorapatite within these zones is rich in inclusions of monazite, iron oxide, and quartz inclusions, plus minor xenotime. Monazite and minor xenotime are also found intergrown as inclusions in the fluorapatite, as well as in surrounding recrystallized magnetite and hematite in the magnetite ore. Monazite and xenotime typically occur as inclusions within both oxides. Monazite-(Ce) and xenotime-(Y) are both relatively poor (<2 wt %) in ThO 2 and UO 2 . No significant compositional differences exist in the (Y + REE) chemistry between monazite and xenotime inclusions in fluorapatite compared to grains intergrown with magnetite and hematite, suggesting that these two REE-rich minerals are cogenetic. Monazite-xenotime geothermometry and geochronology of monazite inclusions in fluorapatite provide evidence that formation/remobilization of the (Y + REE) phosphates took place at ca. 50° to 400°C, approximately 5 to 10 m.y. after emplacement of the main iron oxide-phosphate orebody. Evidence from field relationships and fluid inclusion chemistry, together with the massive recrystallization and remobilization of fluorapatite, monazite, xenotime, and iron oxides at Pea Ridge, suggest a subvolcanic origin coupled with a strong metasomatic reworking of the IOA deposit.

Missouri↗