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At least 919 records · Page 51Linked to original sources

Barcodes are a useful tool for labeling and tracking ecological samples

Barcodes are used to label and track just about everything these days. Look around your office, in your medicine cabinet, at the package you just received in the mail, or on the shelves of any shop in town, and you will immediately grasp the ubiquity of their use. Interestingly, railroads and supermarkets were the early pioneers of barcode development: the former needing a way to track railway car location and ownership on a national scale, the latter needing a way to track a diverse array of products and to decrease checkout times (Nelson 1997). Barcodes first came to use in the sciences via the field of medicine, and the medical literature contains hundreds of publications describing how this technology has reduced errors in patient specimen identification and handling, where error mitigation is crucial. In short, barcodes have been adopted by many industries, and in many fields they are now synonymous with asset tracking. In spite of their potential to efficiently organize “assets” (i.e., samples) and minimize human error, the use of barcodes has yet to gain widespread application in ecology. In an age where students take notes on laptops instead of paper, and where “text messaging” involves a smartphone rather than a ball‐point pen, why do otherwise tech‐savvy ecologists persist in hand‐labeling samples? Why do we repeatedly transcribe long and unique identifiers at each step in the process of sample analysis, thereby wasting time and creating opportunities for transcription errors and data loss? Why are most sample storage areas only successfully navigable by the lab manager who personally shelved the samples? In the case of our large ecology lab—and, we suspect, in many others as well—the answer to these questions was perpetually, “bar‐coding won't be worth the trouble.” Recently, however, we realized this was no longer a sufficient answer when we started a new research project that involved collecting an additional thousands of samples each year; we decided to embrace the tangible benefits of an electronic labeling system, and implemented barcoding in our lab. To be clear, the use of barcoding in ecology is not completely novel, and there have been early adopters of this technology. For example, the Cedar Creek Long Term Ecological Research (LTER) site has been using barcodes since at least the mid‐1990s to track the large number of samples collected in their long‐term experimental grasslands (T. A. Kennedy, personal observation ). Overall, however, Cedar Creek is an outlier: in informal e‐mail surveys of LTER sites, only two of eight respondents used barcodes for sample identification or tracking, and even then their use was generally limited to certain samples or certain stages of sample analysis. Our objective in this article is to use our lab as a case study to highlight the potential of barcodes to simplify numerous aspects of sample collection and processing.

Arizona↗

Experimental investigation of false positive errors in auditory species occurrence surveys

False positive errors are a significant component of many ecological data sets, which in combination with false negative errors, can lead to severe biases in conclusions about ecological systems. We present results of a field experiment where observers recorded observations for known combinations of electronically broadcast calling anurans under conditions mimicking field surveys to determine species occurrence. Our objectives were to characterize false positive error probabilities for auditory methods based on a large number of observers, to determine if targeted instruction could be used to reduce false positive error rates, and to establish useful predictors of among-observer and among-species differences in error rates. We recruited 31 observers, ranging in abilities from novice to expert, that recorded detections for 12 species during 180 calling trials (66,960 total observations). All observers made multiple false positive errors and on average 8.1% of recorded detections in the experiment were false positive errors. Additional instruction had only minor effects on error rates. After instruction, false positive error probabilities decreased by 16% for treatment individuals compared to controls with broad confidence interval overlap of 0 (95% CI: -46 to 30%). This coincided with an increase in false negative errors due to the treatment (26%; -3 to 61%). Differences among observers in false positive and in false negative error rates were best predicted by scores from an online test and a self-assessment of observer ability completed prior to the field experiment. In contrast, years of experience conducting call surveys was a weak predictor of error rates. False positive errors were also more common for species that were played more frequently, but were not related to the dominant spectral frequency of the call. Our results corroborate other work that demonstrates false positives are a significant component of species occurrence data collected by auditory methods. Instructing observers to only report detections they are completely certain are correct is not sufficient to eliminate errors. As a result, analytical methods that account for false positive errors will be needed, and independent testing of observer ability is a useful predictor for among-observer variation in observation error rates.

Ecological Applications↗

The ecology of methane in streams and rivers: Patterns, controls, and global significance

Streams and rivers can substantially modify organic carbon (OC) inputs from terrestrial landscapes, and much of this processing is the result of microbial respiration. While carbon dioxide (CO 2 ) is the major end-product of ecosystem respiration, methane (CH 4 ) is also present in many fluvial environments even though methanogenesis typically requires anoxic conditions that may be scarce in these systems. Given recent recognition of the pervasiveness of this greenhouse gas in streams and rivers, we synthesized existing research and data to identify patterns and drivers of CH 4 , knowledge gaps, and research opportunities. This included examining the history of lotic CH 4 research, creating a database of concentrations and fluxes (MethDB) to generate a global-scale estimate of fluvial CH 4 efflux, and developing a conceptual framework and using this framework to consider how human activities may modify fluvial CH 4 dynamics. Current understanding of CH 4 in streams and rivers has been strongly influenced by goals of understanding OC processing and quantifying the contribution of CH 4 to ecosystem C fluxes. Less effort has been directed towards investigating processes that dictate in situ CH 4 production and loss. CH 4 makes a meager contribution to watershed or landscape C budgets, but streams and rivers are often significant CH 4 sources to the atmosphere across these same spatial extents. Most fluvial systems are supersaturated with CH 4 and we estimate an annual global emission of 26.8 Tg CH 4 , equivalent to ~15-40% of wetland and lake effluxes, respectively. Less clear is the role of CH 4 oxidation, methanogenesis, and total anaerobic respiration to whole ecosystem production and respiration. Controls on CH 4 generation and persistence can be viewed in terms of proximate controls that influence methanogenesis (organic matter, temperature, alternative electron acceptors, nutrients) and distal geomorphic and hydrologic drivers. Multiple controls combined with its extreme redox status and low solubility result in high spatial and temporal variance of CH 4 in fluvial environments, which presents a substantial challenge for understanding its larger-scale dynamics. Further understanding of CH 4 production and consumption, anaerobic metabolism, and ecosystem energetics in streams and rivers can be achieved through more directed studies and comparison with knowledge from terrestrial, wetland, and aquatic disciplines.

Ecological Monographs↗

Relating hyporheic fluxes, residence times, and redox-sensitive biogeochemical processes upstream of beaver dams

Abstract. Small dams enhance the development of patchy microenvironments along stream corridors by trapping sediment and creating complex streambed morphologies. This patchiness drives intricate hyporheic flux patterns that govern the exchange of O 2 and redox-sensitive solutes between the water column and the stream bed. We used multiple tracer techniques, naturally occurring and injected, to evaluate hyporheic flow dynamics and associated biogeochemical cycling and microbial reactivity around 2 beaver dams in Wyoming (USA). High-resolution fiber-optic distributed temperature sensing was used to collect temperature data over 9 vertical streambed profiles and to generate comprehensive vertical flux maps using 1-dimensional (1-D) heat-transport modeling. Coincident with these locations, vertical profiles of hyporheic water were collected every week and analyzed for dissolved O 2 , pH, dissolved organic C, and several conservative and redox-sensitive solutes. In addition, hyporheic and net stream aerobic microbial reactivity were analyzed with a constant-rate injection of the biologically sensitive resazurin (Raz) smart tracer. The combined results revealed a heterogeneous system with rates of downwelling hyporheic flow organized by morphologic unit and tightly coupled to the redox conditions of the subsurface. Principal component analysis was used to summarize the variability of all redox-sensitive species, and results indicated that hyporheic water varied from oxic-stream-like to anoxic-reduced in direct response to the hydrodynamic conditions and associated residence times. The anaerobic transition threshold predicted by the mean O 2 Damko ¨hler number seemed to overestimate the actual transition as indicated by multiple secondary electron acceptors, illustrating the gradient nature of anaerobic transition. Temporal flux variability in low-flux morphologies generated a much greater range in hyporheic redox conditions compared to high-flux zones, and chemical responses to changing flux rates were consistent with those predicted from the empirical relationship between redox condition and residence time. The Raz tracer revealed that hyporheic flow paths have strong net aerobic respiration, particularly at higher residence time, but this reactive exchange did not affect the net stream signal at the reach scale.

Freshwater Science↗

Ore genesis constraints on the Idaho cobalt belt from fluid inclusion gas, noble gas isotope, and ion ratio analyses--a reply

Burlinson (2013) questions the veracity of the H 2 concentrations reported for fluid inclusion extracts from minerals in the Idaho cobalt belt (Table 2; Landis and Hofstra, 2012) and suggests that they are an analytical artifact of electron-impact mass spectrometry. He also declares that H 2 should not be present in fluid inclusions because it is invariably lost by diffusion and is never detected in fluid inclusions by laser Raman. We welcome this opportunity to reply and maintain that the reported H 2 contents are accurate. Below we explain why Burlinson’s criticisms are invalid.

Idaho↗

Time scales of porphyry Cu deposit formation: insights from titanium diffusion in quartz

Porphyry dikes and hydrothermal veins from the porphyry Cu-Mo deposit at Butte, Montana, contain multiple generations of quartz that are distinct in scanning electron microscope-cathodoluminescence (SEM-CL) images and in Ti concentrations. A comparison of microprobe trace element profiles and maps to SEM-CL images shows that the concentration of Ti in quartz correlates positively with CL brightness but Al, K, and Fe do not. After calibrating CL brightness in relation to Ti concentration, we use the brightness gradient between different quartz generations as a proxy for Ti gradients that we model to determine time scales of quartz formation and cooling. Model results indicate that time scales of porphyry magma residence are ~1,000s of years and time scales from porphyry quartz phenocryst rim formation to porphyry dike injection and cooling are ~10s of years. Time scales for the formation and cooling of various generations of hydrothermal vein quartz range from 10s to 10,000s of years. These time scales are considerably shorter than the ~0.6 m.y. overall time frame for each porphyry-style mineralization pulse determined from isotopic studies at Butte, Montana. Simple heat conduction models provide a temporal reference point to compare chemical diffusion time scales, and we find that they support short dike and vein formation time scales. We interpret these relatively short time scales to indicate that the Butte porphyry deposit formed by short-lived episodes of hydrofracturing, dike injection, and vein formation, each with discrete thermal pulses, which repeated over the ~3 m.y. generation of the deposit.

Montana↗

Bobjonesite, V4+ O (SO4) (H2O)3, a new mineral species from Temple Mountain, Emery County, Utah, U.S.A

Bobjonesite, V 4+ O (SO 4 ) (H 2 O) 3 , is a new mineral species from Temple Mountain, Emery County, Utah, U.S.A. It occurs as blue-green crusts and efflorescences in fractures in a fossil (Triassic) tree; individual crystals are <<1 mm and are intimately intergrown. Bobjonesite hydrates very easily, and is unstable in all but the driest atmosphere. Its structure was determined on a crystal of bobjonesite; however, the physical properties, optical properties and X-ray powder-diffraction pattern were recorded on the synthetic equivalent, and an electron-microprobe analysis was not possible. Bobjonesite has a pale blue streak, a vitreous luster and no observable fluorescence under ultraviolet light. It has no cleavage or parting. The Mohs hardness is ~1, and the calculated density is 2.28 g/cm 3 . Bobjonesite is biaxial positive, with α 1.555(2), β 1.561(1), γ 1.574(2), 2 V (obs.) = 72(1)°, 2 V (calc.) = 69°; it is non-pleochroic, X = b , Y ≈ a , Z ∧ c ≈ 19° (in β obtuse). Bobjonesite is monoclinic, space group P 2 1 / n , cell dimensions from single-crystal data: a 7.3940(5), b 7.4111(3), c 12.0597(9) Å, β 106.55(1)°, V 633.5(1) Å 3 , Z = 4. The strongest seven lines in the X-ray powder-diffraction pattern [ d in Å( I )( hkl )] are as follows: 5.795(100)(002), 3.498(90)(112), 3.881(48)(1̅03), 5.408(37) (101), 4.571(20)(012), 6.962(11)(1̅01) and 6.254(11)(011). The chemical formula was derived from crystal-structure analysis; the end-member formula is V O (SO 4 ) (H 2 O) 3 . The crystal structure of bobjonesite was refined to an R index of 3.6% for 1105 observed (| F o | > 5> F ) reflections measured with an automated four-circle X-ray diffractometer using Mo K α X-radiation. There is one V site occupied by V 4+ and surrounded by three O atoms and three (H 2 O) groups in an octahedral arrangement, with one short vanadyl bond (1.577 Å), four similar equatorial bonds (<2.022 Å>), and one longer V–O bond (2.278 Å) trans to the vanadyl bond. The structure consists of isolated [V 4+ 2 O 2 (H 2 O) 6 (SO 4 ) 2 ] clusters linked by hydrogen bonds.

Utah↗

The composition of coexisting jarosite-group minerals and water from the Richmond mine, Iron Mountain, California

Jarosite-group minerals accumulate in the form of stalactites and fine-grained mud on massive pyrite in the D drift of the Richmond mine, Iron Mountain, California. Water samples were collected by placing beakers under the dripping stalactites and by extracting pore water from the mud using a centrifuge. The water is rich in Fe 3+ and SO 4 2− , with a pH of approximately 2.1, which is significantly higher than the extremely acidic waters found elsewhere in the mine. Electron-microprobe analysis and X-ray mapping indicate that the small crystals (<10 μm in diameter) are compositionally zoned with respect to Na and K, and include hydronium jarosite corresponding to the formula (H 3 O) 0.6 K 0.3 Na 0.1 Fe 3 3+ (SO 4 ) 2 (OH) 6 . The proton-microprobe analyses indicate that the jarosite-group minerals contain significant amounts of As, Pb and Zn, and minor levels of Bi, Rb, Sb, Se, Sn and Sr. Speciation modeling indicates that the drip waters are supersaturated with respect to jarosite-group minerals. The expected range in composition of jarosite-group solid-solution in equilibrium with the pore water extracted from the mud was found to be consistent with the observed range in composition.

California↗

High REE and Y concentrations in Co-Cu-Au ores of the Blackbird district, Idaho

Analysis of 11 samples of strata-bound Co-Cu-Au ore from the Blackbird district in Idaho shows previously unknown high concentrations of rare earth elements (REE) and Y, averaging 0.53 wt percent ???REE + Y oxides. Scanning electron microscopy indicates REE and Y residence in monazite, xenotime, and allanite that form complex intergrowths with cobaltite, suggesting coeval Co and REE + Y mineralization during the Mesoproterozoic. Occurrence of high REE and Y concentrations in the Blackbird ores, together with previously documented saline-rich fluid inclusions and Cl-rich biotite, suggest that these are not volcanogenic massive sulfide or sedimentary exhalative deposits but instead are iron oxide-copper-gold (IOCG) deposits. Other strata-bound Co deposits of Proterozoic age in the North American Cordillera and elsewhere in the world may have potential for REE and Y resources. IOCG deposits with abundant light REE should also be evaluated for possible unrecognized heavy REE and Y mineralization. ?? 2006 by Economic Geology.

Economic Geology↗

Bald Mountain gold mining district, Nevada: A Jurassic reduced intrusion-related gold system

The Bald Mountain mining district has produced about 2 million ounces (Moz) of An. Geologic mapping, field relationships, geochemical data, petrographic observations, fluid inclusion characteristics, and Pb, S, O, and H isotope data indicate that An mineralization was associated with a reduced Jurassic intrusion. Gold deposits are localized within and surrounding a Jurassic (159 Ma) quartz monzonite porphyry pluton and dike complex that intrudes Cambrian to Mississippian carbonate and clastic rocks. The pluton, associated dikes, and An mineralization were controlled by a crustal-scale northwest-trending structure named the Bida trend. Gold deposits are localized by fracture networks in the pluton and the contact metamorphic aureole, dike margins, high-angle faults, and certain strata or shale-limestone contacts in sedimentary rocks. Gold mineralization was accompanied by silicification and phyllic alteration, ??argillic alteration at shallow levels. Although An is typically present throughout, the system exhibits a classic concentric geochemical zonation pattern with Mo, W, Bi, and Cu near the center, Ag, Pb, and Zn at intermediate distances, and As and Sb peripheral to the intrusion. Near the center of the system, micron-sized native An occurs with base metal sulfides and sulfosalts. In peripheral deposits and in later stages of mineralization, Au is typically submicron in size and resides in pyrite or arsenopyrite. Electron microprobe and laser ablation ICP-MS analyses show that arsenopyrite, pyrite, and Bi sulfide minerals contain 10s to 1,000s of ppm Au. Ore-forming fluids were aqueous and carbonic at deep levels and episodically hypersaline at shallow levels due to boiling. The isotopic compositions of H and O in quartz and sericite and S and Pb in sulfides are indicative of magmatic ore fluids with sedimentary sulfur. Together, the evidence suggests that Au was introduced by reduced S-bearing magmatic fluids derived from a reduced intrusion. The reduced character of the intrusion was caused by assimilation of carbonaceous sedimentary rocks. Tertiary faults dismember the area and drop down the upper part of the mineralizing system to the west. The abundant and widespread kaolinite in oxide ores is relatively disordered (1A polytype) and has ??D and ??18O values suggestive of a supergene origin. The deep weathering and oxidation of the ores associated with exhumation made them amenable to open-pit mining and processing using cyanide heap leach methods. ?? 2007 Society of Economic Geologists, Inc.

Economic Geology↗

Aurorite, argentian todorokite, and hydrous silver-bearing lead manganese oxide

During a study of hypogene manganese minerals, three silver-bearing manganese oxides were identified in "black calcite" associated with silver ores at the Aurora mine (Treasure Hill), Hamilton, Nevada. Specifically these are: (1) argentian chalcophanite (aurorite) (Ag 2 Ba,Ca,Pb,-K 2 ,Cu,Mn (super +2) )Mn 3 (super +4) O 7 . 3H 2 O; (2) argentian todorokite (Ag 2 ,K 2 ,Ca,Ba,-Na 2 ,Cu,Pb)Mn 4 (super +4) O 9 . 5H 2 O; and (3) hydrous silver-bearing lead manganese oxide (Pb,Cu,Ba,Sb,Ag 2 ,Ca,K 2 )Mn 5 (super +4) O 11 . 5H 2 O. Based on the large concentration of silver in argentian chalcophanite (7.50% Ag 2 O) and the low zinc content (0.25% ZnO) this mineral is recognized as a new species and named "aurorite."Physical and optical properties, and chemical analyses of the three minerals are presented together with X-ray powder diffraction data for aurorite and argentian todorokite. All chemical analyses were done with the electron microprobe analyzer. Due to extremely small particle size and textural relations, no X-ray powder data were obtained for the hydrous silver-bearing lead manganese oxide. Associated minerals include cryptomelane, pyrolusite, birnessite(?), cerargyrite, native silver, quartz, and manganoan calcite. Although the general uniform dark color of the "black calcite" and apparent uniform distribution of the inclusions suggests contemporaneous formation, examination of polished sections at high magnifications shows a definite paragenetic sequence. Manganoan calcite is replaced by fine-grained intergrowths of cryptomelane, pyrolusite, birnessite(?), and cerargyrite. Native silver formed early and the silver-bearing manganese oxides formed late in the sequence; aurorite fills microfractures that cut through all other minerals.These three silver-bearing manganese oxides were recognized only at the Aurora mine, Hamilton, Nevada, although black calcite veins were studied from numerous areas in the western United States. The geologic features of silver-bearing black calcites are described by Hewett and Radtke in the preceding paper.

Nevada↗

Mineralogy of sulfides from certain Hawaiian basalts

Polymineralic sulfide grains, composed principally of Fe sulfide and Fe-Cu sulfide, with magnetite, have been studied mineragraphically and by electron probe, and interpreted in terms of experimental data for the system Fe-Ni-Cu-S. The three main phases are monosulfide solid solution, a Cu-Fe sulfide (solid solution) with composition near cubanite, and Ti-free magnetite. The grains are believed to represent phases unmixed from an immiscible liquid phase in the basalt magma. Compositions of the two main sulfide phases suggest quenching below 700 degrees C. Most of the Ni has been retained in the monosulfide solid solution by rapid quenching.

Hawaii↗

Distribution of silver and copper in placer gold derived from the northeastern part of the Colorado Mineral Belt

Placer gold grains from the modern streams originating in the Colorado Mineral Belt were examined for silver and copper content on a quantitative basis utilizing the electron microprobe. The variation among grains from a particular locality is large, but the mean silver content of the interior of the placer gold grains from each locality and (or) the variation in copper content may be of value in distinguishing lode sources and gold mining districts. Microprobe analysis of the interior of gold grains is independent of chemical actions that affect the border of placer gold grains during their transport history, and it is shown that distinct compositional groups of different lode sources may be identified even in a single sample--information that may aid in recognizing the existence of concealed lodes that once contributed to a placer environment.

Colorado↗

Gold-bearing arsenian pyrite determined by microprobe analysis, Cortez and Carlin Gold Mines, Nevada

Studies of polished sections and chemical analyses made by electron microprobe show that gold and arsenic in the unoxidized ores from the Cortez and Carlin mines are most abundant in pyrite. Gold, as particles too small to be seen under the microscope, along with arsenic is concentrated in tiny pyrite grains (<0.005 mm) and in thin rims of larger pyrite grains. It is concentrated also in arsenopyrite which is sparsely distributed in the Cortez ore. Traces of gold are contained in sphalerite and chalcopyrite sparsely disseminated in Carlin ore. Mercury and antimony occur also in the pyrite, and antimony is in illite as well. Little if any gold or arsenic is contained in quartz, carbonate, clay, and carbonaceous material. In oxidized ore, the sulfur and carbonaceous material have been removed and gold and arsenic occur in iron oxide pseudomorphs after pyrite. Gold can be seen in the oxidized ore, indicating that it has been mobilized and concentrated. No association was found between gold and the carbonaceous material. During mineralization, calcite was removed from the fractured silty carbonate of the Roberts Mountains Formation, creating micropore space in which pyrite, quartz, and illite were deposited. The average tenor of the pyrite, if all the gold were in the pyrite, would be 0.10 percent at Cortez and 0.14 percent at Carlin. These calculated values are similar to the analytical values. The calculated tenor of the carbonaceous material, however-if such material were considered to be the mineral host of the gold-would be 0.28 percent at Cortez and 1 percent at Carlin. These figures are unreasonable when compared with the analytical data, which show that the carbonaceous material contains no detectable amounts of gold. © 1973 Society of Economic Geologists, Inc.

Nevada↗

Annealing history limits for inhomogeneous, native gold grains as determined from Au-Ag diffusion rates

Quantitative study of intrinsic inhomogeneities in native gold grains from three deposits in the western United States has revealed concentration profiles that represent the integrated sum of natural diffusion plus original chemical heterogeneity. By assuming that measured natural concentration gradients result solely from diffusion, upper limits may be placed on the temperature-time annealing history of the gold nuggets. This assumption focuses on the end member case in which an initial step-discontinuity is assumed between measured extremes of concentration.Concentration changes of up to 30 weight percent Ag indicate probable deposition temperatures of less than 300 degrees C for electrum from Copper Basin, Arizona, and Alder Gulch, Montana. The gold in the Homestake, South Dakota, deposit probably was formed at temperatures well under 400 degrees C.In support of this study, new data for interdiffusion in the Au-Ag system were obtained from a series of annealing experiments followed by electron microprobe analysis. The interdiffusion coefficient, D, in the range 10 (super -10) to 10 (super -17) cm 2 sec (super -1) was determined from measured profiles across synthetic alloy pairs held at eight fixed temperatures from 297 degrees to 799 degrees C, for periods ranging from 32 hours to 730 days.

Arizona, Montana, South Dakota↗

Spectra of altered rocks in the visible and near infrared

Visible and near-infrared (0.35 to 2.5 mu m) bidirectional reflection spectra were recorded for a suite of well-characterized hydrothermally altered rock samples. The spectra typically display well-defined bands caused by both electronic and vibrational processes in the individual mineral constituents.Electronic transitions in the iron-bearing constituent minerals produce diagnostic minima near 0.43, 0.65, 0.85, and 0.93 mu m. Vibrational transitions in clay and water-bearing mineral constituents typically produce characteristic single or multiple features over limited spectral ranges near 1.4, 1.75, 1.9, 2.2, and 2.35 mu m. The most abundant feature-producing minerals present in these rocks are hematite, goethite, and alunite, while others frequently present are jarosite, kaolinite, potassium micas, pyrophyllite, montmorillonite, diaspore, and gypsum.This study shows that visible-near infrared spectrometry is a reliable and rapid technique for detecting and identifying clay minerals and alunite in rocks. Because these minerals are important constituents of altered rocks, the feasibility of using the visible and near infrared for detecting altered rocks by remote-sensing techniques is indicated. The spectral region near 2.2 mu m is particularly important for this purpose.

Nevada↗

Near-infrared spectra of West Shasta gossans compared with true and false gossans from Australia and Saudi Arabia

The near-infrared spectra of a suite of outcrop samples of massive sulfide gossans and false gossans representing three different weathering environments were measured and studied with X-ray, scanning electron microscope, and energy dispersive X-ray. Gossans that formed in a humid tropical environment are represented by samples from the Mt. Isa area, Queensland, Australia, and gossans that formed in an arid environment are represented by samples from several locations in Saudi Arabia. The gossans of the West Shasta massive sulfide district in California represent a weathering environment intermediate between these two extremes.On the basis of these spectral measurements, true gossans after massive sulfide deposits have spectra in the 800 to 2,500 nanometer (nm) region that are distinctly different from the spectra of false gossans. In the humid tropical environment, highly leached, newly formed kaolin minerals in the gossan cause spectral differences at about 1,400 to 2,200 nm. In the arid environment, true gossans preserve talc and minor mica from the massive sulfide deposit; these minerals are not observed in false gossans. These minerals result in spectral differences in the 2,200- to 2,300-nm region. In addition, true gossans generally have goethite spectral bands at about 900 nm as opposed to hematite spectral bands at about 850 nm for the false gossans.False gossans are not known in the West Shasta district; however, the gossan at the largest deposit, Iron Mountain, is a true gossan that has the distinctive spectral features of goethite at about 900 nm and diaspore in the 1,400- to 2,500-nm region. The other gossans also have the spectral features of goethite, but they contain a less leached mixture of kaolinite plus illite and have distinctive spectral features in the 1,400- to 2,500-nm region. These spectral differences define two groups of West Shasta gossans--inner gossans in large deposits and outer gossans at the margins of large deposits and in lesser massive sulfide deposits.

Economic Geology↗

A method for the concentration of fine-grained rutile (TiO2) from sediment and sedimentary rocks by chemical leaching

Quaternary marine sediment in the Gulf of Maine basins contains 0.7 to 1.0 wt percent TiO 2 (determined by X-ray fluorescence spectrometry). Most of this TiO 2 exists in the form of silt-size rutile crystals that are visible by using the petrographic microscope with transmitted light (Valentine and Commeau, 1990). The identification of rutile was confirmed by using a scanning electron microscope (SEM) equipped with an energy-dispersive X-ray spectrometer (EDS) system. To quantify the amount of TiO 2 in the sediment contributed by rutile and its polymorphs, anatase and brookite, it was necessary to eliminate as many of the other minerals as possible, especially titanium-bearing minerals such as ilmenite, ilmenomagnetite, biotite, hornblende, oyroxene, and sphene. We accomplished this by developing a method of chemical dissolution that removed the bulk of the raw material and left the TiO 2 minerals intact. Many methods using acids and bases have been developed over the years to dissolve rocks, minerals, and sediments for chemical analysis or to concentrate specific minerals (Dolcater et al., 1970; Church, 1971; Campbell, 1973, and the references cited therein). The method developed by Raman and Jackson (1965) to concentrate rutile and anatase in soils and sediments requires digesting the sample in concentrated hydrofluoric acid (HF) for 24 hours. However, Campbell (1973) found that digestion in HF for more than 2 hours results in a loss of anatase. The method of Dolcater et al. (1970) for concentrating titanium as a free oxide requires the use of hydrofluotitanic acid (H 2 TiF 6 ), which is difficult to find on the commercial market. The acid can be prepared by the reaction of concentrated HF (48%) with an excess of TiO 2 , but the procedure requires 36 hours to complete and should be attempted with caution because it is highly exothermic. Jackson (1979) provides a detailed method for digesting soils, but many of the recommended pretreatment steps employ sodium compounds such as sodium bicarbonate (NaHCO 3 ), sodium citrate (Na 3 C 6 H 5 O 7 -2H 2 O), and sodium dithionate (Na 2 S 2 O 4 ), which are used for the removal of calcium carbonate, iron oxides, and phosphates. In combining the methods of Dolcater and Jackson, sodium compounds must be thoroughly washed from the sample because they form sodium fluotitanate (Na 2 TiF 6 ) in the presence of hydrofluotitanic acid (Fig. 1K). French and Adams (1973) described an inexpensive method for decomposing silicates by HF digestion in polypropylene containers. Their technique was effective for a wide variety of rock types. However, it did not address the problem caused by the precipitation of insoluble fluorides, nor did it outline a procedure to concentrate any residue that remained. As no one method gave the results we required, we modified procedures described in the literature and developed a process that removes 96 to 98 wt percent of the raw sample material. The residue is composed of rutile and minor amounts of micro- and cryptocrystalline TiO 2 (Fig. 1A-J), barite (Fig. 1L), elemental carbon (coal), and insoluble fluorides (Fig. 1J). The fluorides precipitate during the decomposition of siliceous material in hydrofluoric acid (e.g., MgF 2 and MgAlF 5 -2.7H 2 O; Lanmyhr and Kringstad, 1966). Most of the sample analyzed by the method described were marine muds collected from the Gulf of Maine (Valentine and Commeau, 1990). The silt and clay fraction (up to 99 wt% of the sediment) is composed of clay minerals (chiefly illite-mica and chlorite), silt-size quartz and feldspar, and small crystals (2-12 um) of rutile and hematite. The bulk sediment samples contained an average of 2 to 3 wt percent CaCO 3 . Tiher samples analyzed include red and gray Carboniferous and Triassic sandstones and siltstones exposed around the Bay of Fundy region and Paleozoic sandstones, siltstones, and shales from northern Maine and New Brunswick. These rocks are probable sources for the fine-grained rutile found in the Gulf of Maine.

Economic Geology↗