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Bronwen Wang

Publications and source records attributed to Bronwen Wang.

At least 19 recordsLinked to original sources

Earth Mapping Resources Initiative protocols—Sampling hard-rock mine waste and perpetual mine water sources

Supporting the overarching goal to evaluate critical minerals nationwide, the mine waste characterization effort in the U.S. Geological Survey (USGS) Earth Mapping Resources Initiative has created a series of protocols to standardize sampling carried out under this effort by the participating State geological surveys and their cooperators. The protocols are based on published, reviewed methods that can be deployed in the field. The protocols include (1) collecting and processing composite samples of mine and mill waste, including tailings, waste rock, gangue, heap leach piles, ore stockpiles, slag, or other mineralized and processed materials and (2) collecting and preserving water samples from perpetual or long-term mine water sources. The protocols also specify information to document on field sheets and detail the collection of geospatial data. The analytical methods used by the USGS and USGS contract laboratories are described in this report, including the data delivery pathway for USGS-derived data.

Scientific Investigations Report↗

Bayesian mapping of regionally grouped, sparse, univariate earth science data

Some earth science data are naturally grouped by region, and it is often desirable to map these data by region. However, if there are only a few samples within each region, then the map should be smoothed in an appropriate way to mitigate the problems that arise from having only a few samples. A smoothing algorithm based on a Bayesian hierarchical model is developed and presented in this report. This algorithm has several features that make it especially suitable for mapping earth science data: it can account for measurements that are censored, it can process multiple datasets with different measurement errors and different censoring thresholds, and it can calculate the uncertainty in any statistic that is mapped. The algorithm is demonstrated by mapping gold concentrations that are measured in streambed sediments in the Taylor Mountains quadrangle in southwestern Alaska.

Alaska↗

Critical Minerals in Ores (CMiO) database

Critical minerals are commodities essential to modern industrial and strategic technologies and are highly vulnerable to supply chain disruption. The Critical Minerals Mapping Initiative (CMMI) is a collaboration among the U.S. Geological Survey (USGS), the Geological Survey of Canada, and Geoscience Australia that aims to deepen global understanding of where critical minerals are located. A key output of this initiative is the Critical Minerals in Ores (CMiO) database that is advancing our collective understanding of critical minerals distributions. For instance, publicly available data on the concentrations of many critical minerals are sparse because these commodities can only be produced in small, yet essential, quantities compared to the primary commodities like copper and zinc. The CMiO database helps bridge this gap by offering high-quality, multielement geochemical data from a wide variety of critical mineral-bearing deposits around the world. Importantly, it uses a novel consensus deposit environment, group, and type classification scheme developed by the agencies that allows comparisons among ore deposits from different regions. The CMiO database contains geochemical data for more than 20,000 samples from more than 100 deposit types comprising 10 deposit environments.

Fact Sheet↗

From critical minerals to food security, the benefits of data collaboration

The volume of data in the public geoscience sphere is rapidly and continually expanding. At Geoscience Australia (GA) we saw an over 500% increase in data points within our relational databases between 2018 and 2024, over the life of the Exploring for the Future (EFTF) program. With the Resourcing Australia’s Prosperity initiative, a continued increase in data quantity will be seen for the next 10 to 35 years. At the same time, a broadening audience for geoscience data is increasing the desire to enhance the diversity of delivery streams. This ranges from data-dense highly technical outputs for geoscience specialists to curated interpretive products for people who are non-geoscientists. Development of these curated outputs has contributed to our awareness of the need for data to be collected and compiled in a way that ensures its reuse, with a focus on quality metadata and data provenance.

Conference Paper↗

GIS-based identification of areas that have resource potential for lode gold in Alaska

Several comprehensive, data-driven geographic information system (GIS) analyses were conducted to assess prospectivity for lode gold in Alaska. These analyses use available geospatial datasets of lithologic, geochemical, mineral occurrence, and geophysical data to build models for recognizing different types of gold deposits within physiographic units defined by stream drainage basins that are approximately 100 square kilometers in area. The analytical methods successfully delineated areas in the State that contain known lode gold deposits and occurrences, providing some measure of confidence in their ability to predict gold prospectivity in areas of unknown lode gold potential. The results of our analyses indicate high prospectivity in a few areas scattered around the State that are not known to contain lode gold deposits. In addition to assessing the potential for lode gold deposits in Alaska, we designed analyses to distinguish different lode gold deposit types, including orogenic, reduced-intrusion-related, epithermal, and gold-bearing porphyry. These can primarily be differentiated using their unique trace element geochemical fingerprints and elemental enrichments, which reflect the characteristics of the geologic environment and chemistry of the ore-forming fluids. We identified multiple parameters that would discriminate the different types of gold deposits, but owing to the limits of available data, the compositional similarity of ore-forming fluids among some types of lode gold deposits, and overlapping geologic environments, distinguishing deposit types at the state scale in Alaska remains problematic. These limitations resulted in overlapping areas of prospectivity for different deposit types, highlighting the challenges for targeted gold exploration in Alaska. Adjustment of some scoring parameters and recharacterization at smaller scales to highlight individual mineral systems for application of prospectivity analyses may be helpful at a district scale. At a regional scale, the aerial overlap of individual deposit type analyses reinforces confidence in prospectivity for a lode gold resource in a drainage basin. Our analysis for undivided lode gold deposits will be the most practical analysis for landuse decisions in which delineation of areas that have confident potential for gold deposits in general is the primary goal. Data-driven GIS analysis for lode gold potential in Alaska, although limited by the size and uneven coverage of available datasets, objectively indicates prospectivity in areas where exposure is good as well as in areas under cover. The results of our analyses show medium to high prospectivity in areas that surround known deposits, indicating an overall expansion of areas that have the potential to contain gold deposits. Exploration in these areas may help improve the balance between the volume of gold produced in placer districts statewide and the relatively low volume of identified lode resources that contribute to these placer deposits. The results of our analyses can help focus future investigations in areas that show prospectivity but are not known to contain gold deposits, as well as in areas where data are lacking and the geology is poorly understood, and acquisition of additional data may help better define and constrain gold prospectivity.

Alaska↗

Chemical analysis of archived stream-sediment samples, Alaska

Geochemical data are presented for more than 1,500 archived stream-sediment samples and accompanying quality control samples. The archived sediments were reanalyzed to improve the stream geochemical dataset for Alaska and to support ongoing U.S. Geological Survey (USGS) studies. Sediment samples were primarily from the USGS Mineral Resources Program’s sample archive in Denver, Colorado, but a few were from the Alaska Geological & Geophysical Surveys’ Geologic Materials Center in Anchorage, Alaska. All samples were submitted to the USGS contract laboratory, AGAT Laboratories, for analysis. All samples were analyzed using a 60-element analytical method involving fusion of the sample by sodium peroxide, dissolution of the fusion cake by nitric acid, and elemental analysis by inductively coupled plasma-optical emission spectroscopy and inductively coupled plasma-mass spectroscopy. Additionally, 106 samples from the Nixon Fork area were analyzed by a second multi-element method involving decomposition by a mixture of hydrochloric, nitric, perchloric, and hydrofluoric acids and the elemental analysis of the resulting solution by inductively coupled plasma-optical emission spectroscopy and inductively coupled plasma-mass spectroscopy. The latter method was used because the detection limit is lower for several elements including As, Cd, Pb, and Sb. Mercury concentrations in 296 samples from southeast Alaska were determined using a cold-vapor atomic absorption spectrometry method. The concentration data from the archived samples are presented along with concentration data from the standard reference material that was submitted with the samples.

Alaska↗

Evaluation of the analytical methods used to determine the elemental concentrations found in the stream geochemical dataset compiled for Alaska

A recent U.S. Geological Survey data compilation of stream-sediment geochemistry for Alaska contains decades of analyses collected under numerous Federal and State programs. The compiled data were determined by various analytical methods. Some samples were reanalyzed by a different analytical method than the original, resulting in some elements having concentrations reported by multiple analytical methods. Consideration of the analytical methods used to determine the elemental concentrations is an important step in a mineral prospectivity analysis. We used the compiled data to compare concentrations of barium (Ba), cobalt (Co), copper (Cu), chromium (Cr), nickel (Ni), lead (Pb), and zinc (Zn) determined by different analytical methods to show how simple data comparisons can identify bias and provide a general sense of the comparability of different analytical methods. The elements were selected because they have a range of geochemical properties that may affect the performance of different analytical procedures. Generally, agreement between Ba, Co, Cu, Cr, Ni, Pb, and Zn concentrations is good for most quantitative methods that use a total decomposition of the sample. However, Cr concentrations typically were lower for methods using quantitative-instrumental analysis following a multi-acid dissolution technique that included hydrofluoric acid compared to those using sinter decomposition. Additionally, low- to middle-range concentrations for Co, Cr, Cu, Ni, Pb, and Zn by instrumental neutron activation (NA) and energy-dispersive x-ray spectroscopy (EDX) analyzed by the National Uranium Resource Evaluation (NURE) program have high uncertainty. Concentrations determined by methods that use partial decomposition of the sample generally correspond well to concentrations determined by methods that use a total decomposition technique, except for Ba and Cr. For Ba and Cr, partial decomposition techniques yield lower concentrations than those determined by methods that use a total decomposition technique. Comparison of Ba, Co, Cr, Cu, Ni, Pb, and Zn concentrations determined by semiquantitative visual six-step direct-current arc emission spectrography (ES_SQ) to those determined by quantitative methods using either a total or partial decomposition technique consistently show scatter that exceeds the values expected based on the range represented by the semiquantitative concentration. The data compilation includes a best-value determination that was selected based on the analytical method from the all concentration data for that sample. Ba, Cr, Co, and Zn concentrations determined by NA usually are selected as the best-value determination. However, the NURE-NA method was designed for high throughput and the uncertainty associated with low- and mid-range concentrations is greater than that of the multi-acid method used to reanalyze many samples. Selection of the multi-acid method over the NURE-NA method for Ba, Co, and Zn could be warranted. Additionally, concentrations determined by ES_SQ usually are selected as the best-value determination over all methods that use a partial decomposition of the sample. Substitution of concentrations determined by methods that use a partial decomposition for those of ES_SQ may be warranted for Co, Cu, Ni, Pb, and Zn. Regardless of the selection of the best-value determination, the dataset remains a mixed method dataset and the uncertainty due to differences in analytical methodology must be considered when using the dataset.

Alaska↗

Alaska Geochemical Database Version 3.0 (AGDB3)—Including “Best Value” Data Compilations for Rock, Sediment, Soil, Mineral, and Concentrate Sample Media

The Alaska Geochemical Database Version 3.0 (AGDB3) contains new geochemical data compilations in which each geologic material sample has one “best value” determination for each analyzed species, greatly improving speed and efficiency of use. Like the Alaska Geochemical Database Version 2.0 before it, the AGDB3 was created and designed to compile and integrate geochemical data from Alaska to facilitate geologic mapping, petrologic studies, mineral resource assessments, definition of geochemical baseline values and statistics, element concentrations and associations, environmental impact assessments, and studies in public health associated with geology. This relational database, created from data-bases and published datasets of the U.S. Geological Survey (USGS), Atomic Energy Commission National Uranium Resource Evaluation (NURE), Alaska Division of Geological & Geophysical Surveys (DGGS), U.S. Bureau of Mines, and U.S. Bureau of Land Management serves as a data archive in support of Alaskan geologic and geochemical projects and contains data tables in several different formats describing historical and new quantitative and qualitative geochemical analyses. The analytical results were determined by 112 laboratory and field analytical methods on 396,343 rock, sediment, soil, mineral, heavy-mineral concentrate, and oxalic acid leachate samples. Most samples were collected by personnel of these agencies and analyzed in agency laboratories or, under contracts, in commercial analytical laboratories. These data represent analyses of samples collected as part of various agency programs and projects from 1938 through 2017. In addition, mineralogical data from 18,138 nonmagnetic heavy-mineral concentrate samples are included in this database. The AGDB3 includes historical geochemical data archived in the USGS National Geochemical Database (NGDB) and NURE National Uranium Resource Evaluation-Hydrogeochemical and Stream Sediment Reconnaissance databases, and in the DGGS Geochemistry database. Retrievals from these data-bases were used to generate most of the AGDB data set. These data were checked for accuracy regarding sample location, sample media type, and analytical methods used. In other words, the data of AGDB3 supersedes data in the AGDB and the AGDB2, but the background about the data in these two earlier versions are needed by users of the current AGDB3 to understand what has been done to amend, clean up, correct and format this data. Corrections were entered, resulting in a significantly improved Alaska geochemical dataset, the AGDB3. Data that were not previously in these databases because the data predate the earliest agency geochemical data-bases, or were once excluded for programmatic reasons, are included here in the AGDB3 and will be added to the NGDB and Alaska Geochemistry. The AGDB3 data provided here are the most accurate and complete to date and should be useful for a wide variety of geochemical studies. The AGDB3 data provided in the online version of the database may be updated or changed periodically.

Alaska↗

Soil mineralogy and geochemistry along a north-south transect in Alaska and the relation to source-rock terrane

Soils collected along a predominately north-south transect in Alaska were used to evaluate regional differences in the soil mineralogy and geochemistry in the context of a geotectonic framework for Alaska. The approximately 1,395-kilometer-long transect followed the Dalton, Elliott, and Richardson Highways from near Prudhoe Bay to Valdez. Sites were selected with a site spacing of approximately 10 road-kilometers; soil was sampled by soil horizon at 175 sites. Terrane boundaries were estimated from digitized versions of the lithotectonic terrane map of Alaska (Silberling and others, 1994). Terrane assignments for each site were based on the site’s distance along the transect. We also present data for 15 minerals or mineral groups and 58 elements, as well as total, inorganic, and organic carbon. Quantitative mineralogy of the mineral-soil horizons was characterized by X-ray diffraction. Elemental contents were determined by a combination of inductively coupled plasma-atomic emission spectrometry (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS) analysis following a multi-acid or sodium-sinter decomposition of the samples. Total carbon and carbonate carbon contents were determined using an automated carbon analyzer and coulometric titration, respectively; organic carbon content was obtained by calculating the difference between total and carbonate carbon. Mercury and selenium were analyzed using cold-vapor atomic absorption (CV-AA), and hydride-generation atomic absorption spectrometry (HG-AAS), respectively. The mineralogical and geochemical patterns from these soils are used to assess the relation between soil characteristics and the geology of surrounding terranes.

Alaska↗

Fertility of the early post-eruptive surfaces of Kasatochi Island volcano

In the four years after the 2008 eruption and burial of Kasatochi Island volcano, erosion and the return of bird activity have resulted in new and altered land surfaces and initiation of ecosystem recovery. We examined fertility characteristics of the recently deposited pyroclastic surfaces, patches of legacy pre-eruptive surface soil (LS), and a post-eruptive surface with recent bird roosting activity. Pyroclastic materials were found lacking in N, but P, K, and other macronutrients were in sufficient supply for plants. Erosion and leaching are moving mobile P and Fe downslope to deposition fan areas. Legacy soil patches that currently support plants have available-N at levels (10–22 mg N kg -1 ) similar to those added by birds in a recent bird roosting area. Roosting increased surface available N from <1 mg N kg -1 in the new pyroclastic surfaces to up to 42 mg N kg -1 and increased soil biological respiration of CO 2 from essentially zero to a level about 40% that of the LS surface. Laboratory plant growth trials using Lupinus nootkatensis and Leymus mollis indicated that the influence of eroded and redeposited LS in amounts as little as 10% by volume mixed with new pyroclastic materials could aid plant recovery by supplying vital N and soil biota to plants as propagules are introduced to the new surface. Erosion-exposure of fertile pre-eruptive soils and erosion-mixing of pre-eruptive soils with newly erupted materials, along with inputs of nutrients from bird activities, each will exert significant influences on the surface fertility and recovery pattern of the new post-eruptive Kasatochi volcano. For this environment, these influences could help to speed recovery of a more diverse plant community by providing N (LS and bird inputs) as alternatives to relying most heavily on N-fixing plants to build soil fertility.

Alaska↗

The geochemical atlas of Alaska, 2016

A rich legacy of geochemical data produced since the early 1960s covers the great expanse of Alaska; careful treatment of such data may provide significant and revealing geochemical maps that may be used for landscape geochemistry, mineral resource exploration, and geoenvironmental investigations over large areas. To maximize the spatial density and extent of data coverage for statewide mapping of element distributions, we compiled and integrated analyses of more than 175,000 sediment and soil samples from three major, separate sources: the U.S. Geological Survey, the National Uranium Resource Evaluation program, and the Alaska Division of Geological & Geophysical Surveys geochemical databases. Various types of heterogeneity and deficiencies in these data presented major challenges to our development of coherently integrated datasets for modeling and mapping of element distributions. Researchers from many different organizations and disparate scientific studies collected samples that were analyzed using highly variable methods throughout a time period of more than 50 years, during which many changes in analytical techniques were developed and applied. Despite these challenges, the U.S. Geological Survey has produced a new systematically integrated compilation of sediment and soil geochemical data with an average sample site density of approximately 1 locality per 10 square kilometers (km 2 ) for the entire State of Alaska, although density varies considerably among different areas. From that compilation, we have modeled and mapped the distributions of 68 elements, thus creating an updated geochemical atlas for the State.

Alaska↗

Surface-air mercury fluxes across Western North America: A synthesis of spatial trends and controlling variables

Mercury (Hg) emission and deposition can occur to and from soils, and are an important component of the global atmospheric Hg budget. This paper focuses on synthesizing existing surface-air Hg flux data collected throughout the Western North American region and is part of a series of geographically focused Hg synthesis projects. A database of existing Hg flux data collected using the dynamic flux chamber (DFC) approach from almost a thousand locations was created for the Western North America region. Statistical analysis was performed on the data to identify the important variables controlling Hg fluxes and to allow spatiotemporal scaling. The results indicated that most of the variability in soil-air Hg fluxes could be explained by variations in soil-Hg concentrations, solar radiation, and soil moisture. This analysis also identified that variations in DFC methodological approaches were detectable among the field studies, with the chamber material and sampling flushing flow rate influencing the magnitude of calculated emissions. The spatiotemporal scaling of soil-air Hg fluxes identified that the largest emissions occurred from irrigated agricultural landscapes in California. Vegetation was shown to have a large impact on surface-air Hg fluxes due to both a reduction in solar radiation reaching the soil as well as from direct uptake of Hg in foliage. Despite high soil Hg emissions from some forested and other heavily vegetated regions, the net ecosystem flux (soil flux + vegetation uptake) was low. Conversely, sparsely vegetated regions showed larger net ecosystem emissions, which were similar in magnitude to atmospheric Hg deposition (except for the Mediterranean California region where soil emissions were higher). The net ecosystem flux results highlight the important role of landscape characteristics in effecting the balance between Hg sequestration and (re-)emission to the atmosphere.

Science of the Total Environment↗

Biological legacies: Direct early ecosystem recovery and food web reorganization after a volcanic eruption in Alaska

Attempts to understand how communities assemble following a disturbance are challenged by the difficulty of determining the relative importance of stochastic and deterministic processes. Biological legacies, which result from organisms that survive a disturbance, can favour deterministic processes in community assembly and improve predictions of successional trajectories. Recently disturbed ecosystems are often so rapidly colonized by propagules that the role of biological legacies is obscured. We studied biological legacies on a remote volcanic island in Alaska following a devastating eruption where the role of colonization from adjacent communities was minimized. The role of biological legacies in the near shore environment was not clear, because although some kelp survived, they were presumably overwhelmed by the many vagile propagules in a marine environment. The legacy concept was most applicable to terrestrial invertebrates and plants that survived in remnants of buried soil that were exposed by post-eruption erosion. If the legacy concept is extended to include ex situ survival by transient organisms, then it was also applicable to the island's thousands of seabirds, because the seabirds survived the eruption by leaving the island and have begun to return and rebuild their nests as local conditions improve. Our multi-trophic examination of biological legacies in a successional context suggests that the relative importance of biological legacies varies with the degree of destruction, the availability of colonizing propagules, the spatial and temporal scales under consideration, and species interactions. Understanding the role of biological legacies in community assembly following disturbances can help elucidate the relative importance of colonists versus survivors, the role of priority effects among the colonists, convergence versus divergence of successional trajectories, the influence of spatial heterogeneity, and the role of island biogeographical concepts.

Alaska↗

Organic matter quantity and source affects microbial community structure and function following volcanic eruption on Kasatochi Island, Alaska

In August 2008, Kasatochi volcano erupted and buried a small island in pyroclastic deposits and fine ash; since then, microbes, plants and birds have begun to re-colonize the initially sterile surface. Five years post-eruption, bacterial 16S rRNA gene and fungal internal transcribed spacer (ITS) copy numbers and extracellular enzyme activity (EEA) potentials were one to two orders of magnitude greater in pyroclastic materials with organic matter (OM) inputs relative to those without, despite minimal accumulation of OM (<&thinsp;0.2%C). When normalized by OM levels, post-eruptive surfaces with OM inputs had the highest &beta;-glucosidase, phosphatase, NAGase and cellobiohydrolase activities, and had microbial population sizes approaching those in reference soils. In contrast, the strongest factor determining bacterial community composition was the dominance of plants versus birds as OM input vectors. Although soil pH ranged from 3.9 to 7.0, and %C ranged 100&times;, differentiation between plant- and bird-associated microbial communities suggested that cell dispersal or nutrient availability are more likely drivers of assembly than pH or OM content. This study exemplifies the complex relationship between microbial cell dispersal, soil geochemistry, and microbial structure and function; and illustrates the potential for soil microbiota to be resilient to disturbance.

Alaska↗

GIS-Based Identification of Areas with Mineral Resource Potential for Six Selected Deposit Groups, Bureau of Land Management Central Yukon Planning Area, Alaska

This study, covering the Bureau of Land Management (BLM) Central Yukon Planning Area (CYPA), Alaska, was prepared to aid BLM mineral resource management planning. Estimated mineral resource potential and certainty are mapped for six selected mineral deposit groups: (1) rare earth element (REE) deposits associated with peralkaline to carbonatitic intrusive igneous rocks, (2) placer and paleoplacer gold, (3) platinum group element (PGE) deposits associated with mafic and ultramafic intrusive igneous rocks, (4) carbonate-hosted copper deposits, (5) sandstone uranium deposits, and (6) tin-tungsten-molybdenum-fluorspar deposits associated with specialized granites. These six deposit groups include most of the strategic and critical elements of greatest interest in current exploration. This study has used a data-driven, geographic information system (GIS)-based method for evaluating the mineral resource potential across the large region of the CYPA. This method systematically and simultaneously analyzes geoscience data from multiple geospatially referenced datasets and uses individual subwatersheds (12-digit hydrologic unit codes or HUCs) as the spatial unit of classification. The final map output indicates an estimated potential (high, medium, low) for a given mineral deposit group and indicates the certainty (high, medium, low) of that estimate for any given subwatershed (HUC). Accompanying tables describe the data layers used in each analysis, the values assigned for specific analysis parameters, and the relative weighting of each data layer that contributes to the estimated potential and certainty determinations. Core datasets used include the U.S. Geological Survey (USGS) Alaska Geochemical Database (AGDB2), the Alaska Division of Geologic and Geophysical Surveys Web-based geochemical database, data from an anticipated USGS geologic map of Alaska, and the USGS Alaska Resource Data File. Map plates accompanying this report illustrate the mineral prospectivity for the six deposit groups across the CYPA and estimates of mineral resource potential. There are numerous areas, some of them large, rated with high potential for one or more of the selected deposit groups within the CYPA.

Alaska↗

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↗

Effect of ultramafic intrusions and associated mineralized rocks on the aqueous geochemistry of the Tangle Lakes Area, Alaska

Stream water was collected at 30 sites within the Tangle Lakes area of the Delta mineral belt in Alaska. Sampling focused on streams near the ultramafic rocks of the Fish Lake intrusive complex south of Eureka Creek and the Tangle Complex area east of Fourteen Mile Lake, as well as on those within the deformed metasedimentary, metavolcanic, and intrusive rocks of the Specimen Creek drainage and drainages east of Eureka Glacier. Major, minor, and trace elements were analyzed in aqueous samples for this reconnaissance aqueous geochemistry effort. The lithologic differences within the study area are reflected in the major-ion chemistry of the water. The dominant major cation in streams draining mafic and ultramafic rocks is Mg 2+ ; abundant Mg and low Ca in these streams reflect the abundance of Mg-rich minerals in these intrusions. Nickel and Cu are detected in 84 percent and 87 percent of the filtered samples, respectively. Nickel and Cu concentrations ranged from Ni <0.4 to 10.1 micrograms per liter (mg/L), with a median of 4.2 mg/L, and Cu <0.5 to 27 mg/L, with a median of 1.2 mg/L. Trace-element concentrations in water are generally low relative to U.S. Environmental Protection Agency freshwater aquatic-life criteria; however, Cu concentrations exceed the hardness-based criteria for both chronic and acute exposure at some sites. The entire rare earth element (REE) suite is found in samples from the Specimen Creek sites MH5, MH4, and MH6 and, with the exception of Tb and Tm, at site MH14. These samples were all collected within drainages containing or downstream from Tertiary gabbro, diabase, and metagabbro (Trgb) exposures. Chondrite and source rock fractionation profiles for the aqueous samples were light rare earth element depleted, with negative Ce and Eu anomalies, indicating fractionation of the REE during weathering. Fractionation patterns indicate that the REE are primarily in the dissolved, as opposed to colloidal, phase.

Alaska↗

Aqueous geochemical data from the analysis of stream-water samples collected in June and July 2006 — Taylor Mountains 1:250,000-scale quadrangle, Alaska

We report on the chemical analysis of water samples collected from the Taylor Mountains 1:250,000-scale quadrangle, Alaska. Parameters for which data are reported include pH, conductivity, water temperature, major cation and anion concentrations, trace-element concentrations, and dissolved organic-carbon concentrations. Samples were collected as part of a multiyear U.S. Geological Survey project entitled ?Geologic and Mineral Deposit Data for Alaskan Economic Development.? Data presented here are from samples collected in June and July 2006. The data are being released at this time with minimal interpretation. This is the third release of aqueous geochemical data from this project; aqueous geochemical data from samples collected in 2004 and 2005 were published previously. The data in this report augment but do not duplicate or supersede the previous data release. Site selection was based on a regional sampling strategy that focused on first- and second-order drainages. Water sample site selection was based on landscape parameters that included physiography, wetland extent, lithological changes, and a cursory field review of mineralogy from pan concentrates. Stream water in the Taylor Mountains quadrangle is dominated by bicarbonate (HCO3-), although in a few samples more than 50 percent of the anionic charge can be attributed to sulfate (SO42-). The major-cation chemistry ranges from Ca2+/Mg2+ dominated to a mix of Ca2+/Mg2+/Na++K+. Generally, good agreement was found between the major cations and anions in the duplicate samples. Many trace elements in these samples were at or near the analytical method detection limit, but good agreement was found between duplicate samples for elements with detectable concentrations. All field blank major-ion and trace-element concentrations were below detection.

Alaska↗