An ethnoarchaeological study of chemical residues in the floors and soils of Q'eqchi' Maya houses at Las Pozas,Guatemala

This ethnoarchaeological study at the Q'eqchi' Maya village of Las Pozas, Guatemala, aimed to refine the understanding of the relationship between soil chemical signatures and human activities for archaeological applications. The research involved phosphorus, exchangeable ion (calcium, potassium, magnesium, sodium), and trace element analysis of soils and earth floors extracted by Mehlich II, ammonium acetate, and DTPA chelate solutions, respectively. The results showed high levels of phosphorus, potassium, magnesium, and pH in food preparation areas, as well as high phosphorus concentrations and low pH in food consumption areas. The traffic areas exhibited low phosphorus and trace element contents, whereas refuse disposal areas were enriched. These results provide important information for the understanding of space use in ancient settlements. © 2002 Wiley Periodicals, Inc.     

Mineralogy of soils from two continental-scale transects across the United States and Canada and its relation to soil geochemistry and climate

Quantitative mineralogy correlates with major-, minor- and trace-element chemistry for 387 samples of A-horizon and deeper soils collected from east–west and north–south transects across the USA and Canada, where the deeper soils were collected beneath the A-horizon samples. Concentrations of the major elements correlate with specific mineral phases. Minor- and trace-element concentrations correlate with the same phases as the major elements with which they share similar geochemical behavior. Concentrations of quartz and feldspar correlate with precipitation trends east of the Rocky Mountains, and are independent of the underlying rock type and age, indicating that the weathering of soils in this region may have reached a steady-state mineralogy. Other trends in mineralogy relate to physiographic province. The combination of quantitative mineralogy and chemical analysis yields a much richer portrait of soils than can be gained from chemistry alone, because the origins of chemical trends and the chemical availability of specific elements are related to mineralogy.     

Direct observation of heavy metal-mineral association from the Clark Fork River Superfund Complex: Implications for metal transport and bioavailability

Two sets of samples from riverbeds and adjacent floodplains, separated by 80 river kilometers, were collected from the Clark Fork River Superfund Complex, Montana, (the largest Superfund site in the United States), and studied primarily with transmission electron microscopy (TEM) with several supporting techniques to determine heavy metal-mineral association. Seven of the eight samples studied were strongly influenced by material that once resided in mining and smelting dumps and impoundments; this material was transported downstream sometime during the last century and a half from the Butte/Anaconda areas. The eighth sample was from a deeper floodplain level and dates to premining days. The TEM observations afford a direct look, down to the nanometer level, at secondary mineral formation as a result of the breakdown of sulfides and silicates in the acid environment of this massive mine-drainage system. In the shallow, oxic floodplain sediments, heavy metals of concern in this system (As, Cu, Pb, and Zn) are taken up by the formation of sulfates (particularly Pb in jarosite), as well as hydrous metal oxides (As, Cu, Pb, and Zn in and on ferrihydrite, and a possibly new vernadite-like mineral). The oxides are long-lived in these systems, as they were also found in the anoxic riverbeds. Metals are also taken up by the formation of sulfides in sulfate-reducing environments as observed in the formation of nanoclusters of chalcopyrite and sphalerite. In all samples, clays make up between 5 and 20% of the sediment and carry significant amounts of Cu and Zn. The hydrous oxides, secondary sulfides, and clays provide several routes for metal transport downstream over long distances. Besides the potential bioavailability of heavy metals exchanged on and off the hydrous metal oxides and clays, nanometer-sized sulfides may also be highly reactive in the presence of biologic systems.     

Reduction of structural Fe(III) in nontronite by methanogen Methanosarcina barkeri

Clay minerals and methanogens are ubiquitous and co-exist in anoxic environments, yet it is unclear whether methanogens are able to reduce structural Fe(III) in clay minerals. In this study, the ability of methanogen Methanosarcina barkeri to reduce structural Fe(III) in iron-rich smectite (nontronite NAu-2) and the relationship between iron reduction and methanogenesis were investigated. Bioreduction experiments were conducted in growth medium using three types of substrate: H₂/CO₂, methanol, and acetate. Time course methane production and hydrogen consumption were measured by gas chromatography. M. barkeri was able to reduce structural Fe(III) in NAu-2 with H₂/CO₂ and methanol as substrate, but not with acetate. The extent of bioreduction, as measured by the 1,10-phenanthroline method, was 7-13% with H₂/CO₂ as substrate, depending on nontronite concentration (5-10 g/L). The extent was higher when methanol was used as a substrate, reaching 25-33%. Methanogenesis was inhibited by Fe(III) reduction in the H₂/CO₂ culture, but enhanced when methanol was used. High charge smectite and biogenic silica formed as a result of bioreduction. Our results suggest that methanogens may play an important role in biogeochemical cycling of iron in clay minerals and may have important implications for the global methane budget.     

Continental-scale patterns in soil geochemistry and mineralogy: Results from two transects across the United States and Canada

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada (GSC) initiated a pilot study that involved collection of more than 1500 soil samples from 221 sites along two continental transects across Canada and the United States. The pilot study was designed to test and refine protocols for a soil geochemical survey of North America. The two transects crossed a wide array of soil parent materials, soil ages, climatic conditions, landforms, land covers and land uses. Sample sites were selected randomly at approximately 40-km intervals from a population defined as all soils of the continent. At each site, soils representing 0 to 5 cm depth, and the O, A, and C horizons, if present, were collected and analyzed for their near-total content of over 40 major and trace elements. Soils from 0–5 cm depth were also collected for analysis of organic compounds. Results from the transects confirm that soil samples collected at a 40-km spacing reveal coherent, continental- to subcontinental-scale geochemical and mineralogical patterns that can be correlated to aspects of underlying soil parent material, soil age and climate influence. The geochemical data also demonstrate that at the continental-scale the dominance of any of these major factors that control soil geochemistry can change across the landscape. Along both transects, soil mineralogy and geochemistry change abruptly with changes in soil parent materials. However, the chemical influence of a soil’s parent material can be obscured by changing climatic conditions. For the transects, increasing precipitation from west to east and increasing temperature from north to south affect both soil mineralogy and geochemistry because of climate effects on soil weathering and leaching, and plant productivity. Regional anomalous metal concentrations can be linked to natural variations in soil parent materials, such as high Ni and Cr in soils developed on ultramafic rocks in California or high P in soils formed on weathered Ordovician limestones in central Kentucky. On local scales, anomalous metal concentrations recognized in soil profiles, such as high P in soils from animal confinement sites, are consistent with local anthropogenic disturbances. At a larger scale, the distribution of Hg across the west to east transect demonstrates that it can be difficult to distinguish between natural or anthropogenic contributions and that many factors can contribute to an element’s spatial distribution.Only three samples in a subset of seventy-three 0–5 cm depth soil samples from the north to south transect had organochlorine pesticides values above the method detection limit, apparently related to historic usage of the pesticides DDT and dieldrin.     

Soil properties and stable carbon isotope analysis of landscape features in the Petexbatún region of Guatemala

Soil properties and stable carbon isotope ratios contained in the soil organic matter (SOM) were used to investigate the change in vegetative history of land cleared anciently for maize (Zea mays L.) agriculture in the Petexbatún region of Guatemala. Maize and other C⁴ plants associated with land clearance leave a carbon isotopic signature in the SOM different from the C³ plants of native forest vegetation. Soil profiles were collected from various landscape features around the Classic Maya site of Aguateca: control locations (areas likely not used in ancient agriculture), defensible locations (areas near defensive walls), rejolladas (natural karst depressions), upland locations (well‐drained soils atop the Aguateca escarpment), and bajos (seasonal and perennial wetlands). The chemical and physical properties of the profiles were examined and the soils were taxonomically classified to the great group level. The changes in d¹³C with soil depth were determined and compared statistically. The ¹³C enrichment of the SOM in bajo and rejollada profiles were similar and were significantly (p < 0.05) greater than the control, defensible, and upland soils. This isotopic signature of sustained C⁴ vegetation was likely associated with forest clearance and ancient Maya agriculture. Both the bajo and rejollada landscape features appear to have been valuable agricultural resources for ancient Maya. © 2009 Wiley Periodicals, Inc.     

Varying sediment sources (Hudson Strait,Cumberland Sound,Baffin Bay) to the NW Labrador Sea slope between and during Heinrich events 0 to 4

Core HU97048‐007PC was recovered from the continental Labrador Sea slope at a water depth of 945 m, 250 km seaward from the mouth of Cumberland Sound, and 400 km north of Hudson Strait. Cumberland Sound is a structural trough partly floored by Cretaceous mudstones and Paleozoic carbonates. The record extends from ～10 to 58 ka. On‐board logging revealed a complex series of lithofacies, including buff‐colored detrital carbonate‐rich sediments [Heinrich (H)‐events] frequently bracketed by black facies. We investigate the provenance of these facies using quantitative X‐ray diffraction on drill‐core samples from Paleozoic and Cretaceous bedrock from the SE Baffin Island Shelf, and on the < 2‐mm sediment fraction in a transect of five cores from Cumberland Sound to the NW Labrador Sea. A sediment unmixing program was used to discriminate between sediment sources, which included dolomite‐rich sediments from Baffin Bay, calcite‐rich sediments from Hudson Strait and discrete sources from Cumberland Sound. Results indicated that the bulk of the sediment was derived from Cumberland Sound, but Baffin Bay contributed to sediments coeval with H‐0 (Younger Dryas), whereas Hudson Strait was the source during H‐events 1–4. Contributions from the Cretaceous outcrops within Cumberland Sound bracket H‐events, thus both leading and lagging Hudson Strait‐sourced H‐events. Copyright © 2012 John Wiley & Sons, Ltd.     

Black Hole-Neutron Star Mergers as Central Engines of Gamma-Ray Bursts

Hydrodynamic simulations of the merger of stellar mass black hole-neutron star binaries are compared with mergers of binary neutron stars. The simulations are Newtonian but take into account the emission and back-reaction of gravitational waves. The use of a physical nuclear equation of state allows us to include the effects of neutrino emission. For low neutron star-to-black hole mass ratios, the neutron star transfers mass to the black hole during a few cycles of orbital decay and subsequent widening before finally being disrupted, whereas for ratios near unity the neutron star is destroyed during its first approach. A gas mass between approximately 0.3 and approximately 0.7 M middle dot in circle is left in an accretion torus around the black hole and radiates neutrinos at a luminosity of several times 1053 ergs s-1 during an estimated accretion timescale of about 0.1 s. The emitted neutrinos and antineutrinos annihilate into e+/- pairs with efficiencies of 1%-3% and rates of up to approximately 2x1052 ergs s-1, thus depositing an energy Enunu&d1; less, similar1051 ergs above the poles of the black hole in a region that contains less than 10-5 M middle dot in circle of baryonic matter. This could allow for relativistic expansion with Lorentz factors around 100 and is sufficient to explain apparent burst luminosities Lgamma approximately Enunu&d1;&solm0;&parl0;fOmegatgamma&parr0; up to several times 1053 ergs s-1 for burst durations tgamma approximately 0.1-1 s, if the gamma emission is collimated in two moderately focused jets in a fraction fOmega=2deltaOmega&solm0;&parl0;4pi&parr0; approximately 1&solm0;100-(1/10) of the sky.     

Determination of sediment provenance by unmixing the mineralogy of source-area sediments: The “SedUnMix” program

Along the margins of areas such as Greenland and Baffin Bay, sediment composition reflects a complex mixture of sources associated with the transport of sediment in sea ice, icebergs, melt-water and turbidite plumes. Similar situations arise in many contexts associated with sediment transport and with the mixing of sediments from different source areas. The question is: can contributions from discrete sediment (bedrock) sources be distinguished in a mixed sediment by using mineralogy, and, if so, how accurately? To solve this problem, four end-member source sediments were mixed in various proportions to form eleven artificial mixtures. Two of the end-member sediments are felsic, and the other two have more mafic compositions. End member and mixed sediment mineralogies were measured for the < 2 mm sediment fractions by quantitative X-ray diffraction (qXRD). The proportions of source sediments in the mixtures then were calculated using an Excel macro program named SedUnMix, and the results were evaluated to determine the robustness of the algorithm. The program permits the unmixing of up to six end members, each of which can be represented by up to 5 alternative compositions, so as to better simulate variability within each source region. The results indicate that we can track the relative percentages of the four end members in the mixtures. We recommend, prior to applying the technique to down-core or to other provenance problems, that a suite of known, artificial mixtures of sediments from probable source areas be prepared, scanned, analyzed for quantitative mineralogy, and then analyzed by SedUnMix to check the sensitivity of the method for each specific unmixing problem.     

Arsenic in sediments, groundwater, and streamwater of a glauconitic Coastal Plain terrain, New Jersey, USA—Chemical “fingerprints” for geogenic and anthropogenic sources

Glauconite-bearing deposits are found worldwide, but As levels have been determined for relatively few. The As content of glauconites in sediments of the Inner Coastal Plain of New Jersey can exceed 100 mg/kg, and total As concentrations (up to 5.95 μg/L) found historically and recently in streamwaters exceed the State standard. In a major watershed of the Inner Coastal Plain, chemical “fingerprints” were developed for streambed sediments and groundwater to identify contributions of As to the watershed from geologic and anthropogenic sources. The fingerprint for streambed sediments, which included Be, Cr, Fe and V, indicated that As was predominantly of geologic origin. High concentrations of dissolved organic C, nutrients (and Cl⁻) in shallow groundwater indicated anthropogenic inputs that provided an environment where microbial activity released As from minerals to groundwater discharging to the stream. Particulates in streamwater during high flow constituted most of the As load; the chemical patterns for these particulates resembled the geologic fingerprint of the streambed sediments. The As/Cr ratio of these suspended particles likely indicates they derived not only from runoff, but from groundwater inputs, because As contributed by groundwater is sequestered on streambed sediments. Agricultural inputs of As were not clearly identified, although chemical characteristics of some sediments indicated vehicle-related inputs of metals. Sediment sampling during dry and wet years showed that, under differing hydrologic conditions, local anthropogenic fingerprints could be obscured but the geologic fingerprint, indicating glauconitic sediments as an As source, was robust.