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At least 1,621 records · Page 90Linked to original sources

A comparison of geochemical exploration techniques and sample media within accretionary continental margins: an example from the Pacific Border Ranges, Southern Alaska, U.S.A.

The Pacific Border Ranges of the southern Alaskan Cordillera are composed of a number of allochthonous tectonostratigraphic terranes. Within these terranes are widespread volcanogenic, massive sulfide deposits in and adjacent to portions of accreted ophiolite complexes, bands and disseminations of chromite in accreted island-arc ultramafic rocks, and epigenetic, gold-bearing quartz veins in metamorphosed turbidite sequences. A geochemical pilot study was undertaken to determine the most efficient exploration strategy for locating these types of mineral deposits within the Pacific Border Ranges and other typical convergent continental margin environments. High-density sediment sampling was carried out in first- and second-order stream channels surrounding typical gold, chromite and massive sulfide occurrences. At each site, a stream-sediment and a panned-concentrate sample were collected. In the laboratory, the stream sediments were sieved into coarse-sand, fine- to medium-sand, and silt- to clay-size fractions prior to analysis. One split of the panned concentrates was retained for analysis; a second split was further concentrated by gravity separation in heavy liquids and then divided into magnetic, weakly magnetic and nonmagnetic fractions for analysis. A number of different techniques including atomic absorption spectrometry, inductively coupled plasma atomic emission spectrometry and semi-quantitative emission spectrography were used to analyze the various sample media. Comparison of the various types of sample media shows that in this tectonic environment it is most efficient to include a silt- to clay-size sediment fraction and a panned-concentrate sample. Even with the relatively low detection limits for many elements by plasma spectrometry and atomic absorption spectrometry, anomalies reflecting the presence of gold veins could not be identified in any of the stream-sediment fractions. Unseparated panned-concentrate samples should be analyzed by emission spectroscopy and atomic absorption spectrometry for Ag and Au. If, however, magnetic and nonmagnetic concentrate fractions are used in a reconnaissance program, semiquantitative emission spectrography is adequate for all analytical work.

Journal of Geochemical Exploration↗

Fluid inclusion gas chemistry as a potential minerals exploration tool: Case studies from Creede, CO, Jerritt Canyon, NV, Coeur d'Alene district, ID and MT, southern Alaska mesothermal veins, and mid-continent MVT's

Recent advances in instrumentation now permit quantitative analysis of gas species from individual fluid inclusions. Fluid inclusion gas data can be applied to minerals exploration empirically to establish chemical (gas composition) signatures of the ore fluids, and conceptually through the development of genetic models of ore formation from a framework of integrated geologic, geochemical, and isotopic investigations. Case studies of fluid inclusion gas chemistry from ore deposits representing a spectrum of ore-forming processes and environments are presented to illustrate both the empirical and conceptual approaches. We consider epithermal silver-gold deposits of Creede, Colorado, Carlin-type sediment-hosted disseminated gold deposits of Jerritt Canyon, Nevada, metamorphic silver-base-metal veins of the Coeur d'Alene district, Idaho and Montana, gold-quartz veins in accreted terranes of southern Alaska, and the mid-continent base-metal sulfide deposits of Mississippi Valley-Type (MVT's). Variations in gas chemistry determine the redox state of the ore fluids, provide compositional input for gas geothermometers, characterize ore fluid chemistry (e.g., CH 4 CO 2 , H 2 SSO 2 , CO 2 /H 2 S, organic-rich fluids, gas-rich and gas-poor fluids), identify magmatic, meteoric, metamorphic, shallow and deep basin fluids in ore systems, locate upwelling plumes of magmatic-derived volatiles, zones of boiling and volatile separation, interfaces between contrasting fluids, and important zones of fluid mixing. Present techniques are immediately applicable to exploration programsas empirical studies that monitor fluid inclusion gas threshold concentration levels, presence or absence of certain gases, or changes in gas ratios. We suggest that the greater contribution of fluid inclusion gas analysis is in the integrated and comprehensive chemical dimension that gas data impart to genetic models, and in the exploration concepts based on processes and environments of ore formation derived from these genetic models.

Journal of Geochemical Exploration↗

Distribution of modern benthic foraminifers on the New Jersey Outer Continental Shelf

We used samples from 21 stations within a 600 km2 area of the New Jersey Outer Continental Shelf to assess the effects of a hydrodynamic environment on the distribution and redistribution of benthic foraminifers. These samples show that, although the predominant genera (Elphidium, Cibicides, and Saccammina) are the same as those reported by other investigators for this region, the environmental factors that control the generic distribution are more complex than were previously postulated. Generic distribution patterns derived from this study are correlated with the bottom topography and sediment distribution as well as the temperature, salinity, and dissolved oxygen concentrations of the bottom waters. The six predominant species observed in the samples (and their phenotypic variants) are cryophilic forms known to occur in the Virginian and Nova Scotian biogeographic provinces and in Arctic waters. Species distribution patterns also correlate well with bottom topography and hydrographic factors, but may be modified by seasonal fluctuations in test production and by redistribution of dead tests. At most stations, specimens of Elphidium subarcticum were attached to quartz grains. This phenomenon, which has not been reported before, probably is an adaptation to a high-energy environment. The distribution pattern of Elphidium subarcticum along with those of the sessile species Webbinella concava and Vasiglobulina n.sp. corroborate sedimentological evidence that the accumulation of modern sediments in the area is negligible.

New Jersey↗

Neogene biostratigraphy and paleoenvironments of Enewetak Atoll, equatorial Pacific Ocean

Micropaleontologic analyses of Neogene sediments from Enewetak Atoll, Marshall Islands, provide data on the age of lagoonal deposits, stratigraphic disconformities and the paleoenvironmental and subsidence history of the atoll. Benthic foraminifers, planktic foraminifers, calcareous nannofossils and ostracodes were studied from six boreholes, the deepest penetrating 1605 feet below the lagoon floor into upper Oligocene strata. The Oligocene-Miocene boundary occurs at about 1200 ft below the lagoon floor. The early and middle Miocene is characterized by brief periods of deposition and numerous hiatuses. Ostracodes and benthic foraminifers indicate a shallow-marine reefal environment with occasional brackish water conditions. Upper Miocene and lower Pliocene deposits placed in calcareous nannofossil Zones NN9-15 and in planktic foraminifer Zones N16-19 contain species-rich benthic microfaunas which indicate alternating reefal and brackish water mangrove environments. The upper Pliocene contains at least two major depositional hiatuses that coincide with a major faunal turnover in benthic foraminiferal and ostracode assemblages. The Quaternary is characterized by benthic microfaunas similar to those of modern atoll lagoons and is punctuated by at least 11 disconformities which signify periods of low sea level. Atoll subsidence rates during the last 10 Ma averaged 30 to 40 m/m.y. ?? 1991 Elsevier Science Publishers B.V. All rights reserved.

Marine Micropaleontology↗

The applicability of terrestrial visitor impact management strategies to the protection of coral reefs

A dramatic expansion in nature-based tourism to tropical coastal destinations has occurred in the past 20 years. Tourism development, combined with intense recreational pressures, has irreversibly transformed and degraded many popular scenic natural environments. This paper examines the management of recreational impacts to coral reefs using Virgin Islands National Park as a case study. A review of terrestrial recreational ecology research explores the implications and potential applicability of some principal findings to the protection of coral reefs. Visitor impact management recommendations for the protection of coral reefs are offered. Managers can minimize coral reef recreational impacts by (1) restricting high-impact uses, (2) containing rather than dispersing recreational use, (3) encouraging the use of resistant environments, (4) teaching low-impact recreational practices, and (5) enforcing park rules and regulations.

Ocean and Coastal Management↗

The environmental and medical geochemistry of potentially hazardous materials produced by disasters

Many natural or human-caused disasters release potentially hazardous materials (HM) that may pose threats to the environment and health of exposed humans, wildlife, and livestock. This chapter summarizes the environmentally and toxicologically significant physical, mineralogical, and geochemical characteristics of materials produced by a wide variety of recent disasters, such as volcanic eruptions, hurricanes and extreme storms, spills of mining/mineral-processing wastes or coal extraction by-products, and the 2001 attacks on and collapse of the World Trade Center towers. In describing these characteristics, this chapter also illustrates the important roles that geochemists and other earth scientists can play in environmental disaster response and preparedness. In addition to characterizing in detail the physical, chemical, and microbial makeup of HM generated by the disasters, these roles also include (1) identifying and discriminating potential multiple sources of the materials; (2) monitoring, mapping, and modeling dispersal and evolution of the materials in the environment; (3) understanding how the materials are modified by environmental processes; (4) identifying key characteristics and processes that influence the materials' toxicity to exposed humans and ecosystems; (5) estimating shifts away from predisaster environmental baseline conditions; and (6) using geochemical insights learned from past disasters to help estimate, prepare for, and increase societal resilience to the environmental and related health impacts of future disasters.

Book chapter↗

11.12 - Volatile hydrocarbons and fuel oxygenates

Petroleum hydrocarbons and fuel oxygenates are among the most commonly occurring and widely distributed contaminants in the environment. This chapter presents a summary of the sources, transport, fate, and remediation of volatile fuel hydrocarbons and fuel additives in the environment. Much research has focused on the transport and transformation processes of petroleum hydrocarbons and fuel oxygenates, such as benzene, toluene, ethylbenzene, and xylenes and methyl tert‐butyl ether, in groundwater following release from underground storage tanks. Natural attenuation from biodegradation limits the movement of these contaminants and has received considerable attention as an environmental restoration option. This chapter summarizes approaches to environmental restoration, including those that rely on natural attenuation, and also engineered or enhanced remediation. Researchers are increasingly combining several microbial and molecular-based methods to give a complete picture of biodegradation potential and occurrence at contaminated field sites. New insights into the fate of petroleum hydrocarbons and fuel additives have been gained by recent advances in analytical tools and approaches, including stable isotope fractionation, analysis of metabolic intermediates, and direct microbial evidence. However, development of long-term detailed monitoring programs is required to further develop conceptual models of natural attenuation and increase our understanding of the behavior of contaminant mixtures in the subsurface.

Book chapter↗

1.13 – Emerging contaminants

Since the Industrial Revolution, a diversity of large-scale chemical innovations has impacted aquatic systems in urban environments. Beginning in the 1990s, there has been a growing scientific interest and public awareness of the effects of the chemicals used in domestic, commercial, industrial, and agricultural applications, referred to in this article as ‘emerging contaminants’ (ECs), on ecosystem and human health. The growing global population and its increasing demands on water supplies in conjunction with climate-induced changes in hydrologic regimes place stress on freshwater resources, resulting in a greater reliance on reuse of reclaimed municipal wastewater treatment plant (WWTP) effluents to meet human and environmental needs. WWTP effluents are a major source of ECs, and it is important to have an understanding of the chemical composition of the reclaimed water, because many ECs are biologically active and the effects of chronic exposure to low concentration complex mixtures are unknown. Several classes of ECs that have been shown to be widespread in the aquatic environment are discussed in this chapter, including surfactants, complexing agents, fragrances, antimicrobials, industrial chemicals, pharmaceuticals, natural and synthetic estrogens, and disinfection byproducts. All of these compounds are biologically active via a variety of modes of action, and can occur in aquatic systems at concentrations ranging from <0.001 to >100 μg l −1 .

Book chapter↗

The global dispersion of pathogenic microorganisms by dust storms and its relevance to agriculture

Dust storms move an estimated 500–5000 Tg of soil through Earth’s atmosphere every year. Dust-storm transport of topsoils may have positive effects such as fertilization of aquatic and terrestrial ecosystems and the evolution of soils in proximal and distal environments. Negative effects may include the stripping of nutrient-rich topsoils from source regions, sandblasting of plant life in downwind environments, the fertilization of harmful algal blooms, and the transport of toxins (e.g., metals, pesticides, herbicides, etc.) and pathogenic microorganisms. With respect to the long-range dispersion of microorganisms and more specifically pathogens, research is just beginning to demonstrate the quantity and diversity of organisms that can survive this type of transport. Most studies to date have utilized different assays to identify microorganisms and microbial communities using predominately culture-based, and more recently nonculture-based, methodologies. There is a clear need for international-scale research efforts that apply standardized methods to advance this field of science. Here we present a review of dust-borne microorganisms with a focus on their relevance to agronomy.

Book chapter↗

Evaluating the status of individuals and populations: Advantages of multiple approaches and time scales

The assessment of population status is a central goal of applied wildlife research and essential to the field of wildlife conservation. &ldquo;Population status&rdquo; has a number of definitions, the most widely used having to do with the current trajectory of the population (i.e., growing, stable, or declining), or the probability of persistence (i.e., extinction risk), perhaps without any specific knowledge as to the factors driving a population&rsquo;s dynamics. In contrast, a population&rsquo;s status relative to the carrying capacity of the environment ( K ) is an ecologically-based definition that explicitly provides information about a major mechanism of population control. That is, it relates to the relative per capita availability of resources to individuals in a population, which can also be used to infer the state of the environment itself. Sea otters in the North Pacific provide an excellent system with which to examine various approaches to assessing population status relative to K . This is because sea otters were nearly extirpated by historic commercial overexploitation in the eighteenth and nineteenth centuries, followed by natural and translocation-aided population recovery during the twentieth century, and this decline and recovery has been relatively well documented. This provided a unique opportunity to study populations at the extremes of the population status spectrum. Here we describe and review the approaches that have been utilized in sea otter research to understand the status of populations relative to resource abundance. Specifically, we will illustrate the utility of various indices of population status for understanding population dynamics using the case study of a second precipitous sea otter decline in the Western Aleutians. The indices or &ldquo;tools&rdquo; described here fit into several broad categories including (1) energetic, (2) morphological, and (3) demographic as well as a fourth category of emerging tools that have not yet been employed in many other situations including dietary diversity, community structure, spatial distribution, and gene expression. Overall, a variety of indices used to measure population status throughout the sea otter&rsquo;s range have provided insights for understanding the mechanisms driving the trajectory of various sea otter populations, which a single index could not, and we suggest using multiple methods to measure a population&rsquo;s status at multiple spatial and temporal scales. The work described here also illustrates the usefulness of long-term data sets and/or approaches that can be used to assess population status retrospectively, providing information otherwise not available. While not all systems will be as amenable to using all the approaches presented here, we expect innovative researchers could adapt analogous multi-scale methods to a broad range of habitats and species including apex predators occupying the top trophic levels, which are often of conservation concern.

Book chapter↗

Radionuclides in surface water and groundwater

Unique among all the contaminants that adversely affect surface- and groundwater quality, radioactive compounds pose a double threat from toxicity and ionizing radiation. The high energy potential of many of these materials makes them both useful and hazardous. The unique properties of radioactive materials make them invaluable for medical and energy applications. However, mining, production, use, and disposal of compounds and their byproducts provide potential pathways for their release into the environment, posing a risk to both humans and ecosystems. This chapter presents an overview of the sources and uses of radioactive compounds in the United States, biogeochemical processes that control mobility in the environment, examples of radionuclide contamination, and an overview of remediation strategies.

Book chapter↗

Sea otter-mediated linkages among oceanic, nearshore, and terrestrial ecosystems

Seemingly distinct ecological communities are often linked by both direct and indirect interactions that can be difficult to discern. A widely recognized interecosystem linkage is the transfer of marine-derived nutrients to terrestrial systems via anadromous fish. In this chapter, we explore other linkages that move marine-derived nutrients between ocean and terrestrial ecosystems, focusing on the role of nearshore marine ecosystems . Through oceanic nutrients and biomass that originate from phytoplankton, and nearshore nutrients and biomass that derive mainly from macroalgae, there are multiple pathways to subsidize terrestrial ecosystems. We discuss various pathways identified through multiple independent studies and explore how those subsidies may be related to sea otter presence. Recovery of sea otters and subsequent changes to nearshore communities, for example, changes in kelp, invertebrate and vertebrate abundance, and diversity, may in turn influence coastal terrestrial ecosystems and species including bears, wolves, foxes, river otters, shorebirds, and other consumers. As offshore oceanic productivity declines globally, we ask how the return of the sea otter reinvigorates diminished and lost linkages between marine and terrestrial environments through direct predator–prey linkages, and indirectly through the enhancement of the nearshore marine environment.

Book chapter↗

Pleistocene Lake Bonneville as an analog for extraterrestrial lakes and oceans

Geomorphic confirmation for a putative ancient Mars ocean relies on analog comparisons of coastal-like features such as shoreline feature attributes and temporal scales of process formation. Pleistocene Lake Bonneville is one of the few large, geologically young, terrestrial lake systems that exemplify well-preserved shoreline characteristics that formed quickly, on the order of a thousand years or less. Studies of Lake Bonneville provide two essential analog considerations for interpreting shorelines on Mars: (1) morphological variations in expression depend on constructional vs erosional processes, and (2) shorelines are not always correlative at an equipotential elevation across a basin due to isostasy, heat flow, wave setup, fetch, and other factors. Although other large terrestrial lake systems display supporting evidence for geomorphic comparisons, Lake Bonneville encompasses the most integrated examples of preserved coastal features related to basin history, sediment supply, climate, and fetch, all within the context of a detailed hydrograph. These collective terrestrial lessons provide a framework to evaluate possible boundary conditions for ancient Mars hydrology and large water body environmental feedbacks. This knowledge of shoreline characteristics, processes, and environments can support explorations of habitable environments and guide future mission explorations.

Book chapter↗

Applied aspects of locomotion and biomechanics

Locomotion is the act and process of moving from place to place, which is fundamental to the life history of all mobile organisms. While the field of biomechanics encompasses the study of the physical constraints of what animals are capable of, ecological contexts require an integrated view that includes ecology and behavior. This chapter provides an overview of some of the areas where locomotion and biomechanics of fish movement interface with the rapidly evolving changes that humans impose on aquatic environments. These changes include fundamental alterations to the environment such as altered flows, fragmentation of riverine habitats, and invasive species, but also direct interactions that occur with capture fisheries. We explore each of these areas, considering both challenges and opportunities informed by the study of locomotion and biomechanics, emphasizing how this field can contribute to conservation of fishes in the Anthropocene. We then turn to technology, where important advances are aiding in our understanding of fish movement. In some cases those advances have themselves led to novel technologies, where biomimetic robots and related devices offer novel opportunities, both for conservation and for other pursuits.

Book chapter↗

Weathering of the New Albany Shale, Kentucky: II. Redistribution of minor and trace elements

During weathering, elements enriched in black shale are dispersed in the environment by aqueous and mechanical transport. Here a unique evaluation of the differential release, transport, and fate of Fe and 15 trace elements during progressive weathering of the Devonian New Albany Shale in Kentucky is presented. Results of chemical analyses along a weathering profile (unweathered through progressively weathered shale to soil) describe the chemically distinct pathways of the trace elements and the rate that elements are transferred into the broader, local environment. Trace elements enriched in the unweathered shale are in massive or framboidal pyrite, minor sphalerite, CuS and NiS phases, organic matter and clay minerals. These phases are subject to varying degrees and rates of alteration along the profile. Cadmium, Co, Mn, Ni, and Zn are removed from weathered shale during sulfide-mineral oxidation and transported primarily in aqueous solution. The aqueous fluxes for these trace elements range from 0.1 g/ha/a (Cd) to 44 g/ha/a (Mn). When hydrologic and climatic conditions are favorable, solutions seep to surface exposures, evaporate, and form Fe-sulfate efflorescent salts rich in these elements. Elements that remain dissolved in the low pH (<4) streams and groundwater draining New Albany Shale watersheds become fixed by reactions that increase pH. Neutralization of the weathering solution in local streams results in elements being adsorbed and precipitated onto sediment surfaces, resulting in trace element anomalies. Other elements are strongly adsorbed or structurally bound to solid phases during weathering. Copper and U initially are concentrated in weathering solutions, but become fixed to modern plant litter in soil formed on New Albany Shale. Molybdenum, Pb, Sb, and Se are released from sulfide minerals and organic matter by oxidation and accumulate in Fe-oxyhydroxide clay coatings that concentrate in surface soil during illuviation. Chromium, Ti, and V are strongly correlated with clay abundance and considered to be in the structure of illitic clay. Illite undergoes minimal alteration during weathering and is concentrated during illuvial processes. Arsenic concentration increases across the weathering profile and is associated with the succession of secondary Fe(III) minerals that form with progressive weathering. Detrital fluxes of particle-bound trace elements range from 0.1 g/ha/a (Sb) to 8 g/ha/a (Mo). Although many of the elements are concentrated in the stream sediments, changes in pH and redox conditions along the sediment transport path could facilitate their release for aqueous transport.

Applied Geochemistry↗

Characteristics and environmental aspects of slag: a review

Slag is a waste product from the pyrometallurgical processing of various ores. Based on over 150 published studies, this paper provides an overview of mineralogical and geochemical characteristics of different types of slag and their environmental consequences, particularly from the release of potentially toxic elements to water. This chapter reviews the characteristics of both ferrous (steel and blast furnace Fe) and non-ferrous (Ag, Cu, Ni, Pb, Sn, Zn) slag. Interest in slag has been increasing steadily as large volumes, on the order of hundreds of millions of tonnes, are produced annually worldwide. Research on slag generally focuses on potential environmental issues related to the weathering of slag dumps or on its utility as a construction material or reprocessing for secondary metal recovery. The chemistry and mineralogy of slag depend on the metallurgical processes that create the material and will influence its fate as waste or as a reusable product. The composition of ferrous slag is dominated by Ca and Si. Steel slag may contain significant Fe, whereas Mg and Al may be significant in Fe slag. Calcium-rich olivine-group silicates, melilite-group silicates that contain Al or Mg, Ca-rich glass, and oxides are the most commonly reported major phases in ferrous slag. Calcite and trace amounts of a variety of sulfides, intermetallic compounds, and pure metals are typically also present. The composition of non-ferrous slag, most commonly from base-metal production, is dominated by Fe and Si with significant but lesser amounts of Al and Ca. Silicates in the olivine, pyroxene, and melilite groups, as well as glass, spinels, and SiO 2 (i.e., quartz and other polymorphs) are commonly found in non-ferrous slag. Sulfides and intermetallic compounds are less abundant than the silicates and oxides. The concentrations of some elements exceed generic USEPA soil screening levels for human contact based on multiple exposure pathways; these elements include Al, Cr, Cu, Fe, Mn, Pb, and Zn based on bulk chemical composition. Each slag type usually contains a specific suite of elements that may be of environmental concern. In general, non-ferrous slag may have a higher potential to negatively impact the environment compared to ferrous slag, and is thus a less attractive material for reuse, based on trace element chemistry, principally for base metals. However, the amount of elements released into the environment is not always consistent with bulk chemical composition. Many types of leaching tests have been used to help predict slag&rsquo;s long-term environmental behavior. Overall, ferrous slags produce an alkaline leachate due to the dissolution of Ca oxides and silicates derived from compounds originally added as fluxing agents, such as lime. Ferrous slag leachate is commonly less metal-rich than leachate from non-ferrous slag generated during base metal extraction; the latter leachate may even be acidic due to the oxidation of sulfides. Because of its characteristics, ferrous slag is commonly used for construction and environmental applications, whereas both non-ferrous and ferrous slag may be reprocessed for secondary metal recovery. Both types of slag have been a source of some environmental contamination. Research into the environmental aspects of slag will continue to be an important topic whether the goal is its reuse, recycling, or remediation.

Applied Geochemistry↗

Arsenic and antimony geochemistry of mine wastes, associated waters and sediments at the Giant Mine, Yellowknife, Northwest Territories, Canada

Elevated levels of arsenic (As) and antimony (Sb) in water and sediments are legacy residues found downstream from gold-mining activities at the Giant Mine in Yellowknife, Northwest Territories (NWT), Canada. To track the transport and fate of As and Sb, samples of mine-waste from the mill, and surface water, sediment, pore-water, and vegetation downstream of the mine were collected. Mine waste, pore-water, and sediment samples were analyzed for bulk chemistry, and aqueous and solid-state speciation. Sediment and vegetation chemistry were evaluated using scanning electron microscope imaging, synchrotron-based element mapping and electron microprobe analysis. The distributions of As and Sb in sediments were similar, yet their distributions in the corresponding pore-waters were mostly dissimilar, and the mobility of As was greater than that of Sb. Competition for sorption sites is the most likely cause of elevated Sb concentrations in relatively oxidized pore-water and surface water. The aqueous and solid-state speciation of As and Sb also differed. In pore-water, As(V) dominated in oxidizing environments and As(III) in reducing environments. In contrast, the Sb(V) species dominated in all but one pore-water sample, even under reducing conditions. Antimony(III) appears to preferentially precipitate or adsorb onto sulfides as evidenced by the prevalence of an Sb(III)-S secondary solid-phase and the lack of Sb(III)(aq) in the deeper zones. The As(V)–O solid phase became depleted with depth below the sediment–water interface, and the Sb(V)–O phase persisted under relatively reducing conditions. In the surficial zone at a site populated by Equisetum fluviatile (common horsetail), As and Sb were associated with organic material and appeared mobile in the root zone. In the zone below active plant growth, As and Sb were associated primarily with inorganic phases suggesting a release and reprecipitation of these elements upon plant death. The co-existence of reduced and oxidized As and Sb species, instability of some phases under changing redox conditions, and plant uptake and release pose challenges for remediation efforts at the mine.

Northwest Territories↗

Antimony mobility during the early stages of stibnite weathering in tailings at the Beaver Brook Sb deposit, Newfoundland

The aqueous speciation and mineralogy of antimony (Sb) in waters and tailings at Beaver Brook antimony deposit have been analyzed to understand Sb mobility during the initial stages of stibnite (Sb2S3) weathering in a near-surface environment. Dissolution of stibnite in oxidizing conditions releases Sb in drainage water and Sb is incorporated into the mineral structures of several secondary minerals. The most abundant Sb host in Beaver Brook tailings is primary stibnite, which dissolves, releasing Sb(III) to the pore water which rapidly oxidizes to Sb¬(V). The maximum concentration of Sb in tailings pore water is 26.4 mg/L and only 0.9% is in form of Sb(III). In all surface water, Sb concentration ranges from 0.01 to 26.1 mg/L (average 9.4 mg/L) and is mostly present in its Sb(V) (98.9 to 99.2 % of total Sb). The secondary minerals containing Sb formed in tailings impoundment, include tripuhyite-like Sb-Fe oxides (FeSbO4) where Sb is an important part of their structure with variable Fe/Sb ratios and Sb concentrations of up to 37.8% by weight (average of 21.7%). These are important Sb host phases in the top 30 cm of tailings. Iron oxides enriched in Sb, such as goethite (FeOOH), where Sb (average of 3.9% by weight) is adsorbed or incorporated in the structure are common but represent less than 1.3 % of the total mass of Sb. The elevated Mg concentrations in tailing ponds and pore water promote the precipitation of brandholzite (Mg[Sb(OH)6]2·6H2O) (in association with gypsum) during dry periods, which is easily dissolved during rainy periods. Brandholzite dissolution may significantly contribute to the concentration of dissolved Sb, together with stibnite dissolution, whereas Sb-Fe oxides are stable in the neutral pH, oxidized surface environment. Arsenic (As) accompanies Sb in all media but its behaviour differs from that of Sb. The source of As is arsenopyrite, which decomposes more slowly than stibnite. This may be due to the formation of oxidation rims on arsenopyrite grains composed of Fe, As, S, Sb and Ca which slow the dissolution, whereas no rims are seen on stibnite. Also, despite similar As and Sb concentration in bulk tailings, the concentration of Sb in drainage water is higher than that of As. In pore water, As(III) is the dominant oxidation state of As suggesting that the oxidation of dissolved As is slower than that of Sb.

Newfoundland↗