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At least 865 records · Page 48Linked to original sources

USGS2011

The effects of permafrost thaw on soil hydrologic, thermal, and carbon dynamics in an Alaskan peatland

Recent warming at high-latitudes has accelerated permafrost thaw in northern peatlands, and thaw can have profound effects on local hydrology and ecosystem carbon balance. To assess the impact of permafrost thaw on soil organic carbon (OC) dynamics, we measured soil hydrologic and thermal dynamics and soil OC stocks across a collapse-scar bog chronosequence in interior Alaska. We observed dramatic changes in the distribution of soil water associated with thawing of ice-rich frozen peat. The impoundment of warm water in collapse-scar bogs initiated talik formation and the lateral expansion of bogs over time. On average, Permafrost Plateaus stored 137 ± 37 kg C m -2 , whereas OC storage in Young Bogs and Old Bogs averaged 84 ± 13 kg C m -2 . Based on our reconstructions, the accumulation of OC in near-surface bog peat continued for nearly 1,000 years following permafrost thaw, at which point accumulation rates slowed. Rapid decomposition of thawed forest peat reduced deep OC stocks by nearly half during the first 100 years following thaw. Using a simple mass-balance model, we show that accumulation rates at the bog surface were not sufficient to balance deep OC losses, resulting in a net loss of OC from the entire peat column. An uncertainty analysis also revealed that the magnitude and timing of soil OC loss from thawed forest peat depends substantially on variation in OC input rates to bog peat and variation in decay constants for shallow and deep OC stocks. These findings suggest that permafrost thaw and the subsequent release of OC from thawed peat will likely reduce the strength of northern permafrost-affected peatlands as a carbon dioxide sink, and consequently, will likely accelerate rates of atmospheric warming.

Alaska↗

USGS2018

Beyond clay: Towards an improved set of variables for predicting soil organic matter content

Improved quantification of the factors controlling soil organic matter (SOM) stabilization at continental to global scales is needed to inform projections of the largest actively cycling terrestrial carbon pool on Earth, and its response to environmental change. Biogeochemical models rely almost exclusively on clay content to modify rates of SOM turnover and fluxes of climate-active CO 2 to the atmosphere. Emerging conceptual understanding, however, suggests other soil physicochemical properties may predict SOM stabilization better than clay content. We addressed this discrepancy by synthesizing data from over 5,500 soil profiles spanning continental scale environmental gradients. Here, we demonstrate that other physicochemical parameters are much stronger predictors of SOM content, with clay content having relatively little explanatory power. We show that exchangeable calcium strongly predicted SOM content in water-limited, alkaline soils, whereas with increasing moisture availability and acidity, iron- and aluminum-oxyhydroxides emerged as better predictors, demonstrating that the relative importance of SOM stabilization mechanisms scales with climate and acidity. These results highlight the urgent need to modify biogeochemical models to better reflect the role of soil physicochemical properties in SOM cycling.

Biogeochemistry↗

USGS2023

Foliar chemical composition and respiration rates of sugar maple (Acer saccharum) and American beech (Fagus grandifolia) trees across a gradient of soil acidification

Acidic deposition has been well studied for its impacts on forest soils and plants and is thought to detrimentally affect sugar maple ( Acer saccharum ) in northeastern North America. The physiological mechanism driving reduced tree growth on acid impaired sites is not well understood, but has been suggested to involve increased autotrophic respiration rates. We measured foliar respiration and leaf elemental composition on two species with contrasting acid tolerances (sugar maple and American beech, Fagus grandifolia ) across a naturally occurring soil base saturation (BS) gradient in the Adirondack Mountains of New York. Foliar chemistry varied strongly as anticipated across the BS gradient, with decreases in base cations and increases in phytotoxic metals (e.g., Mn) on sites with highly acidified soils. However, foliar respiration rates were not correlated with most measures of acidity (e.g., BS, foliar concentrations of Ca, Mg, Al content). Respiration rates did correlate with other leaf traits (N content, leaf mass per unit area) reflective of leaf morphological variation in response to variable light availability. After accounting for multivariate trait covariation, mass-based respiration rates were associated with foliar Mn content, suggesting a positive relationship between the concentration of this phytotoxic metal and foliar respiration rates. Soluble foliar Ca, Mg, and Mn were closely correlated with total foliar concentrations of these elements. Overall these results demonstrate that soil acidification and loss of base cations is largely unrelated to foliar respiration rates, although the accumulation of foliar Mn on acidified soils may contribute to the metabolic burden of both sugar maple and American beech trees.

New York↗

USGS2020

Soil surface elevation dynamics in a mangrove-to-marsh ecotone characterized by vegetation shifts

Mangrove forest encroachment into coastal marsh habitats has been described in subtropical regions worldwide in recent decades. To better understand how soil processes may influence vegetation change, we studied soil surface elevation change, accretion rates, and soil subsurface change across a coastal salinity gradient in Florida, USA, an area with documented mangrove encroachment into saline marshes. Our aim was to identify if variations in the soil variables studied exist and to document any associated vegetation shifts. We used surface elevation tables and marker horizons to document the soil variables over 5 years in a mangrove-to-marsh transition zone or ecotone. Study sites were located in three marsh types (brackish, salt, and transition) and in riverine mangrove forests. Mangrove forest sites had significantly higher accretion rates than marsh sites and were the only locations where elevation gain occurred. Significant loss in surface elevation occurred at transition and salt marsh sites. Transition marshes, which had a significantly higher rate of shallow subsidence compared to other wetland types, appear to be most vulnerable to submergence or to a shift to mangrove forest. Submergence can result in herbaceous vegetation mortality and conversion to open water, with severe implications to the quantity and quality of wetland services provided.

Florida↗

USGS2010

Soil and periphyton indicators of anthropogenic water-quality changes in a rainfall-driven wetland

Surface soils and periphyton communities were sampled across an oligotrophic, soft-water wetland to document changes associated with pulsed inputs of nutrient- and mineral-rich canal drainage waters. A gradient of canal-water influence was indicated by the surface-water specific conductance, which ranged between 743 and 963 μS cm −1 in the canals to as low as 60 μS cm −1 in the rainfall-driven wetland interior. Changes in soil chemistry and periphyton taxonomic composition across this gradient were described using piecewise regressions models. The greatest increase in soil phosphorus (P) concentration occurred at sites closest to the canal while soil mineral (sulfur, calcium) concentrations increased most rapidly at the lower end of the gradient. Multiple periphyton shifts occurred at the lower end of the gradient and included; (1) a decline in desmids and non-desmid filamentous chlorophytes, and their replacement by a diatom-dominated community; (2) the loss of soft-water diatom indicator species and their replacement by hard-water species. Increased dominance by cyanobacteria and eutrophic diatom indicators occurred closer to the canals. Soil and periphyton changes indicated four zones of increasing canal influence across the wetland: (1) a zone of increasing mineral concentrations where soft-water taxa remained dominant; (2) a transition towards hard-water, oligotrophic diatoms as mineral concentrations increased further; (3) a zone of dominance by these hard-water species; (4) a zone of rapidly increasing P concentrations and dominance by eutrophic taxa. In contrast to conclusions drawn from routine water-chemistry monitoring, measures of chemical and biological change presented here indicate that most of this rainfall-driven peatland receives some influence from canal discharges. These changes are multifaceted and induced by shifts in multiple chemical constituents.

Florida↗

USGS2013

H-binding of size- and polarity-fractionated soil and lignite humic acids after removal of metal and ash components

A fractionation technique, combining dialysis removal of metal and ash components with hydrofluoric acid and pH 10 citrate buffer followed by chromatography of dialysis permeate on XAD-8 resin at decreasing pH values, has been applied to lignite humic acid (lignite-HA) and soil humic acid (soil-HA). H-binding data and non ideal competitive adsorption-Donnan model parameters were obtained for the HA fractions by theoretical analysis of H-binding data which reveal a significant increase of the carboxyl and the phenolic charge for the lignite-HA fractions vs. the parental lignite humic acid (L Parental HA). The fractionated lignite-HA material consisted mainly of permeate fractions, some of which were fulvic acid-like. The fractionated soil-HA material consisted mainly of large macromolecular structures that did not permeate the dialysis membrane during deashing. Chargeable groups had comparable concentrations in soil-HA fractions and parental soil humic acid (S Parental HA), indicating minimal interference of ash components with carboxyl and phenolic (and/or enolic) groups. Fractionation of HA, combined with theoretical analysis of H-binding, can distinguish the supramolecular vs. macromolecular nature of fractions within the same parental HA.

Environmental Science and Pollution Research↗

USGS2011

Soil characteristics of sediment-amended baldcypress ( Taxodium distichum ) swamps of coastal Louisiana

Amendments of sediment from dredging activities have played an important role in raising the elevation of sinking coastal wetlands. This study compared the soil characteristics of sediment- amended coastal swamps in the Barataria Preserve unit of Jean Lafitte National Historical Park and Preserve with natural swamps along Bayou des Familles. The sandy sediment amendments used in the coastal forests had different soil texture and characteristics than the more organic soils of the natural swamps. Three years after the application of these sediments on the sediment-amended swamps, dewatering and compaction of the sediment had occurred but the sediment still had high salinity and bulk density, and low organic matter content. The two sediment-amended swamps differed from each other in that Site 1 had a higher elevation (mean = 25 cm higher) and drier soil than Site 2. The effects of sediment in coastal forested wetlands require separate consideration from studies of salt marshes, e.g., the weight of the sediment might damage tree roots, or the amendments might influence soil stability during storms in a different way. Generally, this study suggests that shallower depths of sediment are more likely to yield environments beneficial to these sinking baldcypress swamps in coastal Louisiana.

Louisiana↗

USGS1990

Soil development on stable landforms and implications for landscape studies

Soil development parameters include a wide variety of morphological, chemical, and mineralogical parameters, but some of the best indicators of time and surface stability are derived from field morphology. Over long time-spans, the most common time function for soil development is exponential or logarithmic, in which rates decrease with increasing age. Over shorter time-spans in semi-arid and moister climates, Holocene and Pleistocene soil development functions appear as linear segments, with Holocene rates about 10 to 50 times those of Pleistocene rates. In contrast to significant temporal variation in rates, geographical variation in rates within (a) the southern Great Basin and (b) the east Central Valley of California is on the order of 2 or 3 times. When comparing soil development indices of the semi-arid Great Basin to those of moister central California, Holocene rates are similar, but Pleistocene rates are more than 10 times slower in the Great Basin. In a range of climatic settings, the reasons for declining rates over time are several and are complexly related to erosional history, fluxes in water and dust related to climatic changes, rates of primary mineral dissolution, and intrinsic soil processes.

Geomorphology↗

USGS1985

Crystalline gold in soil and the problem of supergene nugget formation: Freezing and exclusion as genetic mechanisms

Many of the world's richest gold placer deposits now occur in cold regions despite differences in their climatic history. It therefore seems possible that there may be some fundamental connection between freezing climates and the local chemical behavior of gold in the weathering cycle. This hypothesis, along with the problematical occurrence of gold as euhedral crystals in arctic gravel and soil placers, has led me to review low temperature phenomena that may bear on the geochemistry of gold. Several effects which may influence the weathering of natural gold-bearing rocks, the chemical complexation of gold, and its subsequent mobility and deposition appear to be strongly connected with freeze action. The exclusion of dissolved solutes, solute gases, and particles from ice, subjects rock and soil minerals to increased corrosion from thin, unfrozen, adsorbed water films which remain at particle surfaces throughout the freezing of rocks and soils. The preferential exclusion of cations (over anions) from growing ice crystals creates charge separations and measurable current flow across waterice phase boundaries in freezing soil — a phenomenon which leads to troublesome seasonal electrolytic corrosion of pipelines buried in soil; this phenomenon may also favor the dissolution of normally insoluble metals such as gold during geologic time periods. The ice-induced accumulation of clays, organic acids, bacteria, and other organic matter at mineral surfaces may also speed chemical attack by providing a nearby sink of alternate cation-binding sites and hence rapid removal of liberated cations from solution. The latter mechanism may be operative in both the dissolution and redeposition of gold. These physical, chemical, and electrical effects are favorable to the dissolution of rocks (in addition to frost shattering) and to the dissolution, mobilization, and redeposition of gold and other noble metals and must therefore contribute significantly to the behavior of gold at low temperatures. The occurrence of large numbers of gold placer deposits in northern Canada, Alaska, and Siberia may thus be due in part to the low temperatures common to these regions.

Precambrian Research↗

USGS1993

Evidence for Holocene stability of steep slopes, northern Peruvian Andes, based on soils and radiocarbon dates

Radiocarbon dating and soil relationships indicate that landscapes in highaltitude glaciated valleys of the northern Peruvian Andes have been remarkably stable during the Holocene. Radiocarbon dates show that deglaciation was underway by 12 ka, and that slopes and alluvial fans at the bases of slopes were essentially stabilized by at least 8 ka. The soils consist of fine-grained loessial A horizons overlying Bw horizons in gravelly till or alluvial-fan gravel. Following deglaciation, widespread gullying took place in till on the steep (maximum angle: 37°) sideslopes of most valleys; the eroded material was deposited as fans at the bases of the slopes. Loess was then deposited as a fairly uniform blanket across most elements of the landscape. Soil formation began during or following loess deposition, and because soil-profile morphology is sufficiently similar at most sites, soil formation has been a dominant process during much of the Holocene. This remarkable stability, especially for such steep slopes, is attributed to a combination of tight packing of the till, permeability of the capping loess, rapid revegetation following ice retreat, and roots from the present grassland vegetation and possibly former forests.

Catena↗

USGS2012

Advances in spectroscopic methods for quantifying soil carbon

The current gold standard for soil carbon (C) determination is elemental C analysis using dry combustion. However, this method requires expensive consumables, is limited by the number of samples that can be processed (~100/d), and is restricted to the determination of total carbon. With increased interest in soil C sequestration, faster methods of analysis are needed, and there is growing interest in methods based on diffuse reflectance spectroscopy in the visible, near-infrared or mid-infrared spectral ranges. These spectral methods can decrease analytical requirements and speed sample processing, be applied to large landscape areas using remote sensing imagery, and be used to predict multiple analytes simultaneously. However, the methods require localized calibrations to establish the relationship between spectral data and reference analytical data, and also have additional, specific problems. For example, remote sensing is capable of scanning entire watersheds for soil carbon content but is limited to the surface layer of tilled soils and may require difficult and extensive field sampling to obtain proper localized calibration reference values. The objective of this chapter is to discuss the present state of spectroscopic methods for determination of soil carbon.

Book chapter↗

USGS2020

Soil biogeochemical responses of a tropical forest to warming and hurricane disturbance

Tropical forests represent <15% of Earths terrestrial surface yet support >50% of the planets species and play a disproportionately large role in determining climate due to the vast amounts of carbon they store and exchange with the atmosphere. Currently, disturbance patterns in tropical ecosystems are changing due to factors such as increased land use pressure and an occurrence of hurricanes. At the same time, these regions are expected to experience unprecedented warming before 2100. Despite the importance of these ecosystems for forecasting the global consequences of multiple stressors, our understanding of how projected changes in climate and disturbance will affect the biogeochemical cycling of tropical forests remains in its infancy. Until now, no studies to our knowledge have evaluated forest recovery following hurricane disturbance within the context of concurrent climatic change. Here, we present soil biogeochemical results from a tropical forest field warming experiment in Puerto Rico where, a year after experimental warming began, Hurricanes Irma and Mara greatly altered the forest, allowing a unique opportunity to explore the interacting effects of hurricane disturbance and warming. We tracked post-hurricane forest recovery for a year without warming to assess legacy effects of prior warming on the disturbance response, and then reinitiated warming treatments to further evaluate interactions between forest recovery and warmer temperatures. The data showed that warming affected multiple aspects of soil biogeochemical cycling even in the first year of treatment, with particularly large positive effects on soil microbial biomass pools (e.g., increases of 54, 43, and 46% relative to the control plots were observed for microbial biomass carbon, nitrogen, and phosphorus, respectively after 6 months of warming). We also observed significant effects of the hurricanes on soil biogeochemical cycling, as well as interactive controls of warming and disturbance. Taken together, our results showed dynamic soil responses that suggest the future of biogeochemical cycling in this tropical wet forest will be strongly shaped by the directional effects of warming and the episodic effects of hurricanes.

Puerto Rico↗

USGS2015

Corn Belt soil carbon and macronutrient budgets with projected sustainable stover harvest

Corn ( Zea mays L.) stover has been identified as a prime feedstock for biofuel production in the U.S. Corn Belt because of its perceived abundance and availability, but long-term stover harvest effects on regional nutrient budgets have not been evaluated. We defined the minimum stover requirement (MSR) to maintain current soil organic carbon levels and then estimated current and future soil carbon (C), nitrogen (N), phosphorus (P), and potassium (K) budgets for various stover harvest scenarios. Analyses for 2006 through 2010 across the entire Corn Belt indicated that currently, 28 Tg or 1.6 Mg ha −1 of stover could be sustainably harvested from 17.95 million hectares (Mha) with N, P, and K removal of 113, 26, and 47 kg ha −1 , respectively, and C removal for that period was estimated to be 4.55 Mg C ha −1 . Assuming continued yield increases and a planted area of 26.74 Mha in 2050, 77.4 Tg stover (or 2.4 Mg ha −1 ) could be sustainably harvested with N, P, and K removal of 177, 37, and 72 kg ha −1 , respectively, along with C removal of &sim;6.57 Mg C ha −1 . Although there would be significant variation across the region, harvesting only the excess over the MSR under current fertilization rates would result in a small depletion of soil N (−5 ± 27 kg ha −1 ) and K (−20 ± 31 kg ha −1 ) and a moderate surplus of P (36 ± 18 kg ha −1 ). Our 2050 projections based on continuing to keep the MSR, but having higher yields indicate that soil N and K deficits would become larger, thus emphasize the importance of balancing soil nutrient supply with crop residue removal.

Iowa, Illinois, Indiana, Michigan, Minnesota, Miss↗

USGS2016

Hyperspectral narrowband and multispectral broadband indices for remote sensing of crop evapotranspiration and its components (transpiration and soil evaporation)

Evapotranspiration (ET) is an important component of micro- and macro-scale climatic processes. In agriculture, estimates of ET are frequently used to monitor droughts, schedule irrigation, and assess crop water productivity over large areas. Currently, in situ measurements of ET are difficult to scale up for regional applications, so remote sensing technology has been increasingly used to estimate crop ET. Ratio-based vegetation indices retrieved from optical remote sensing, like the Normalized Difference Vegetation Index (NDVI), Soil Adjusted Vegetation Index, and Enhanced Vegetation Index are critical components of these models, particularly for the partitioning of ET into transpiration and soil evaporation. These indices have their limitations, however, and can induce large model bias and error. In this study, micrometeorological and spectroradiometric data collected over two growing seasons in cotton, maize, and rice fields in the Central Valley of California were used to identify spectral wavelengths from 428 to 2295 nm that produced the highest correlation to and lowest error with ET, transpiration, and soil evaporation. The analysis was performed with hyperspectral narrowbands (HNBs) at 10 nm intervals and multispectral broadbands (MSBBs) commonly retrieved by Earth observation platforms. The study revealed that (1) HNB indices consistently explained more variability in ET (Δ R 2 = 0.12), transpiration (Δ R 2 = 0.17), and soil evaporation (Δ R 2 = 0.14) than MSBB indices; (2) the relationship between transpiration using the ratio-based index most commonly used for ET modeling, NDVI, was strong ( R 2 = 0.51), but the hyperspectral equivalent was superior ( R 2 = 0.68); and (3) soil evaporation was not estimated well using ratio-based indices from the literature (highest R 2 = 0.37), but could be after further evaluation, using ratio-based indices centered on 743 and 953 nm ( R 2 = 0.72) or 428 and 1518 nm ( R 2 = 0.69).

California↗

USGS2016

Assessing the evolution of soil moisture and vegetation conditions during the 2012 United States flash drought

This study examines the evolution of several model-based and satellite-derived drought metrics sensitive to soil moisture and vegetation conditions during the extreme flash drought event that impacted major agricultural areas across the central U.S. during 2012. Standardized anomalies from the remote sensing based Evaporative Stress Index (ESI) and Vegetation Drought Response Index (VegDRI) and soil moisture anomalies from the North American Land Data Assimilation System (NLDAS) are compared to the United States Drought Monitor (USDM), surface meteorological conditions, and crop and soil moisture data compiled by the National Agricultural Statistics Service (NASS). Overall, the results show that rapid decreases in the ESI and NLDAS anomalies often preceded drought intensification in the USDM by up to 6 wk depending on the region. Decreases in the ESI tended to occur up to several weeks before deteriorations were observed in the crop condition datasets. The NLDAS soil moisture anomalies were similar to those depicted in the NASS soil moisture datasets; however, some differences were noted in how each model responded to the changing drought conditions. The VegDRI anomalies tracked the evolution of the USDM drought depiction in regions with slow drought development, but lagged the USDM and other drought indicators when conditions were changing rapidly. Comparison to the crop condition datasets revealed that soybean conditions were most similar to ESI anomalies computed over short time periods (2–4 wk), whereas corn conditions were more closely related to longer-range (8–12 wk) ESI anomalies. Crop yield departures were consistent with the drought severity depicted by the ESI and to a lesser extent by the NLDAS and VegDRI datasets.

Agricultural and Forest Meteorology↗

USGS2009

Pilot studies for the North American Soil Geochemical Landscapes Project - Site selection, sampling protocols, analytical methods, and quality control protocols

In 2004, the US Geological Survey (USGS) and the Geological Survey of Canada sampled and chemically analyzed soils along two transects across Canada and the USA in preparation for a planned soil geochemical survey of North America. This effort was a pilot study to test and refine sampling protocols, analytical methods, quality control protocols, and field logistics for the continental survey. A total of 220 sample sites were selected at approximately 40-km intervals along the two transects. The ideal sampling protocol at each site called for a sample from a depth of 0-5 cm and a composite of each of the O, A, and C horizons. The <2-mm fraction of each sample was analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, As, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y, and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO 3 , HClO 4 , and HF. Separate methods were used for Hg, Se, total C, and carbonate-C on this same size fraction. Only Ag, In, and Te had a large percentage of concentrations below the detection limit. Quality control (QC) of the analyses was monitored at three levels: the laboratory performing the analysis, the USGS QC officer, and the principal investigator for the study. This level of review resulted in an average of one QC sample for every 20 field samples, which proved to be minimally adequate for such a large-scale survey. Additional QC samples should be added to monitor within-batch quality to the extent that no more than 10 samples are analyzed between a QC sample. Only Cr (77%), Y (82%), and Sb (80%) fell outside the acceptable limits of accuracy (% recovery between 85 and 115%) because of likely residence in mineral phases resistant to the acid digestion. A separate sample of 0-5-cm material was collected at each site for determination of organic compounds. A subset of 73 of these samples was analyzed for a suite of 19 organochlorine pesticides by gas chromatography. Only three of these samples had detectable pesticide concentrations. A separate sample of A-horizon soil was collected for microbial characterization by phospholipid fatty acid analysis (PLFA), soil enzyme assays, and determination of selected human and agricultural pathogens. Collection, preservation and analysis of samples for both organic compounds and microbial characterization add a great degree of complication to the sampling and preservation protocols and a significant increase to the cost for a continental-scale survey. Both these issues must be considered carefully prior to adopting these parameters as part of the soil geochemical survey of North America.

Applied Geochemistry↗

USGS2011

A national-scale geochemical and mineralogical survey of soils of the conterminous United States

In 2007, the US Geological Survey initiated a low-density (1 site per 1600 km 2 , c. 4800 sites) geochemical and mineralogical survey of soils of the conterminous USA. The ideal sampling protocol at each site includes a sample from 0–5 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The <2-mm fraction of each sample is analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO 3 , HClO 4 and HF. Separate methods are used for As, Hg, Se and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling was completed in 2010 with chemical and mineralogical analysis currently underway. Preliminary results for a swath from the central USA to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.

Conterminous United States↗

USGS2009

Changing sources of strontium to soils and ecosystems across the Hawaiian Islands

Strontium isotope ratios assist ecosystem scientists in constraining the sources of alkaline earth elements, but their interpretation can be difficult because of complexities in mineral weathering and in the geographical and environmental controls on elemental additions and losses. Hawaii is a "natural laboratory" where a number of important biogeochemical variables have either limited ranges or vary in systematic ways, providing a unique opportunity to understand the impact of time, climate, and atmospheric inputs on the evolution of base cation sources to ecosystems. There are three major sources of strontium (Sr) to these ecosystems, each with distinct isotopic compositions: basalt lava, Asian dust, and rainfall. We present Sr isotope and concentration data on both bulk soil digests and NH 4 Ac extracts from soil profiles covering a wide range of environments and substrate ages. Bulk soil material from dry climates and/or young substrate ages with > 80????g g - 1 Sr retain basalt-like Sr isotopic signatures, whereas those with Sr concentrations < 80????g g - 1 can have isotope signatures that range from basalt-like values to the more radiogenic values associated with continental dust. Although both dust accumulation and lava weathering are time- and rainfall-dependent, the overall concentration of Sr drops with increasing leaching even as quartz and mica derived from continental dust sources increase to > 40% by mass. At elevated dust levels, lava-derived Sr is low and dust-derived Sr is the dominant control of 87 Sr/ 86 Sr in bulk soils; however, 87 Sr/ 86 Sr of NH 4 Ac-extractable Sr largely reflects atmospheric deposition of marine aerosol in these situations. Overall, whole-soil Sr isotope values are controlled by complex interactions between Sr provided by lava weathering but partially lost by leaching, and Sr provided by dust but held in more resistant minerals. The isotopic composition of NH 4 Ac-extractable Sr and of the biota is controlled by lava weathering and rainfall contribution of Sr with only minor contributions from radiogenic dust sources. ?? 2009 Elsevier B.V.

Chemical Geology↗