Depth-Dependent Mineral Soil CO2 Production Processes: Sensitivity to Harvesting-Induced Changes in Soil Climate.

Science.gov (United States)

Kellman, Lisa; Myette, Amy; Beltrami, Hugo

2015-01-01

Forest harvesting induces a step change in the climatic variables (temperature and moisture), that control carbon dioxide (CO2) production arising from soil organic matter decomposition within soils. Efforts to examine these vertically complex relationships in situ within soil profiles are lacking. In this study we examined how the climatic controls on CO2 production change within vertically distinct layers of the soil profile in intact and clearcut forest soils of a humid temperate forest system of Atlantic Canada. We measured mineral soil temperature (0, 5, 10, 20, 50 and 100 cm depth) and moisture (0-15 cm and 30-60 cm depth), along with CO2 surface efflux and subsurface concentrations (0, 2.5, 5, 10, 20, 35, 50, 75 and 100 cm depth) in 1 m deep soil pits at 4 sites represented by two forest-clearcut pairs over a complete annual cycle. We examined relationships between surface efflux at each site, and soil heat, moisture, and mineral soil CO2 production. Following clearcut harvesting we observed increases in temperature through depth (1-2°C annually; often in excess of 4°C in summer and spring), alongside increases in soil moisture (30%). We observed a systematic breakdown in the expected exponential relationship between CO2 production and heat with mineral soil depth, consistent with an increase in the role moisture plays in constraining CO2 production. These findings should be considered in efforts to model and characterize mineral soil organic matter decomposition in harvested forest soils.

Molecular Studies of Complex Soil Organic Matter Interactions with Metal Ions and Mineral Surfaces using Classical Molecular Dynamics and Quantum Chemistry Methods

Science.gov (United States)

Andersen, A.; Govind, N.; Laskin, A.

2017-12-01

Mineral surfaces have been implicated as potential protectors of soil organic matter (SOM) against decomposition and ultimate mineralization to small molecules which can provide nutrients for plants and soil microbes and can also contribute to the Earth's elemental cycles. SOM is a complex mixture of organic molecules of biological origin at varying degrees of decomposition and can, itself, self-assemble in such a way as to expose some biomolecule types to biotic and abiotic attack while protecting other biomolecule types. The organization of SOM and SOM with mineral surfaces and solvated metal ions is driven by an interplay of van der Waals and electrostatic interactions leading to partitioning of hydrophilic (e.g. sugars) and hydrophobic (e.g., lipids) SOM components that can be bridged with amphiphilic molecules (e.g., proteins). Classical molecular dynamics simulations can shed light on assemblies of organic molecules alone or complexation with mineral surfaces. The role of chemical reactions is also an important consideration in potential chemical changes of the organic species such as oxidation/reduction, degradation, chemisorption to mineral surfaces, and complexation with solvated metal ions to form organometallic systems. For the study of chemical reactivity, quantum chemistry methods can be employed and combined with structural insight provided by classical MD simulations. Moreover, quantum chemistry can also simulate spectroscopic signatures based on chemical structure and is a valuable tool in interpreting spectra from, notably, x-ray absorption spectroscopy (XAS). In this presentation, we will discuss our classical MD and quantum chemistry findings on a model SOM system interacting with mineral surfaces and solvated metal ions.

The nanophase iron mineral(s) in Mars soil

Science.gov (United States)

Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

1993-01-01

A series of surface-modified clays containing nanophase (np) iron oxide/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these "Mars-soil analogs" were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging, specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The clay acted as an effective matrix, both chemically and sterically, preventing the major part of the synthesized iron oxides from ripening, i.e., growing and developing larger crystals. The precipitated iron oxides appear as isodiametric or slightly elongated particles in the size range 1-10 nm, having large specific surface area. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxy mineral such as "green rust," or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable maghemite (gamma-Fe2O3) by mild heat treatment and then to nanophase hematite (alpha-Fe2O3) by extensive heat treatment. After mild heating, the iron-enriched clay became slightly magnetic, to the extent that it adheres to a hand-held magnet, as was observed with Mars soil. The chemical reactivity of the iron-enriched clays strongly resembles, and offers a plausible mechanism

Uranium Sequestration by Aluminum Phosphate Minerals in Unsaturated Soils

International Nuclear Information System (INIS)

Jerden, James L. Jr.

2007-01-01

A mineralogical and geochemical study of soils developed from the unmined Coles Hill uranium deposit (Virginia) was undertaken to determine how phosphorous influences the speciation of uranium in an oxidizing soil/saprolite system typical of the eastern United States. This paper presents mineralogical and geochemical results that identify and quantify the processes by which uranium has been sequestered in these soils. It was found that uranium is not leached from the saturated soil zone (saprolites) overlying the deposit due to the formation of a sparingly soluble uranyl phosphate mineral of the meta-autunite group. The concentration of uranium in the saprolites is approximately 1000 mg uranium per kg of saprolite. It was also found that a significant amount of uranium was retained in the unsaturated soil zone overlying uranium-rich saprolites. The uranium concentration in the unsaturated soils is approximately 200 mg uranium per kg of soil (20 times higher than uranium concentrations in similar soils adjacent to the deposit). Mineralogical evidence indicates that uranium in this zone is sequestered by a barium-strontium-calcium aluminum phosphate mineral of the crandallite group (gorceixite). This mineral is intimately inter-grown with iron and manganese oxides that also contain uranium. The amount of uranium associated with both the aluminum phosphates (as much as 1.4 weight percent) has been measured by electron microprobe micro-analyses and the geochemical conditions under which these minerals formed has been studied using thermodynamic reaction path modeling. The geochemical data and modeling results suggest the meta-autunite group minerals present in the saprolites overlying the deposit are unstable in the unsaturated zone soils overlying the deposit due to a decrease in soil pH (down to a pH of 4.5) at depths less than 5 meters below the surface. Mineralogical observations suggest that, once exposed to the unsaturated environment, the meta-autunite group

Microbial community responses in forest mineral soil to compaction, organic matter removal, and vegetation control

Science.gov (United States)

Matt D. Busse; Samual E. Beattie; Robert F. Powers; Filpe G. Sanchez; Allan E. Tiarks

2006-01-01

We tested three disturbance hypotheses in young conifer plantations: H1: soil compaction and removal of surface organic matter produces sustained changes in microbial community size, activity, and structure in mineral soil; H2: microbial community characteristics in mineral soil are linked to the recovery of plant diversity...

Microbial Composition in Decomposing Pine Litter Shifts in Response to Common Soil Secondary Minerals

Science.gov (United States)

Welty-Bernard, A. T.; Heckman, K.; Vazquez, A.; Rasmussen, C.; Chorover, J.; Schwartz, E.

2011-12-01

A range of environmental and biotic factors have been identified that drive microbial community structure in soils - carbon substrates, redox conditions, mineral nutrients, salinity, pH, and species interactions. However, soil mineralogy has been largely ignored as a candidate in spite of recent studies that indicate that minerals have a substantial impact on soil organic matter stores and subsequent fluxes from soils. Given that secondary minerals and organic colloids govern a soil's biogeochemical activity due to surface area and electromagnetic charge, we propose that secondary minerals are a strong determinant of the communities that are responsible for process rates. To test this, we created three microcosms to study communities during decomposition using pine forest litter mixed with two common secondary minerals in soils (goethite and gibbsite) and with quartz as a control. Changes in bacterial and fungal communities were tracked over the 154-day incubation by pyrosequencing fragments of the bacterial 16S and fungal 18S rRNA genes. Ordination using nonmetric multidimensional scaling showed that bacterial communities separated on the basis of minerals. Overall, a single generalist - identified as an Acidobacteriaceae isolate - dominated all treatments over the course of the experiment, representing roughly 25% of all communities. Fungal communities discriminated between the quartz control alone and mineral treatments as a whole. Again, several generalists dominated the community. Coniochaeta ligniaria dominated communities with abundances ranging from 29 to 40%. The general stability of generalist populations may explain the similarities between treatment respiration rates. Variation between molecular fingerprints, then, were largely a function of unique minor members with abundances ranging from 0.01 to 8%. Carbon availability did not surface as a possible mechanism responsible for shifts in fingerprints due to the relatively large mass of needles in the

Mercury contamination in agricultural soils from abandoned metal mines classified by geology and mineralization.

Science.gov (United States)

Kim, Han Sik; Jung, Myung Chae

2012-01-01

This survey aimed to compare mercury concentrations in soils related to geology and mineralization types of mines. A total of 16,386 surface soils (0~15 cm in depth) were taken from agricultural lands near 343 abandoned mines (within 2 km from each mine) and analyzed for Hg by AAS with a hydride-generation device. To meaningfully compare mercury levels in soils with geology and mineralization types, three subclassification criteria were adapted: (1) five mineralization types, (2) four valuable ore mineral types, and (3) four parent rock types. The average concentration of Hg in all soils was 0.204 mg kg(-1) with a range of 0.002-24.07 mg kg(-1). Based on the mineralization types, average Hg concentrations (mg kg(-1)) in the soils decreased in the order of pegmatite (0.250) > hydrothermal vein (0.208) > hydrothermal replacement (0.166) > skarn (0.121) > sedimentary deposits (0.045). In terms of the valuable ore mineral types, the concentrations decreased in the order of Au-Ag-base metal mines ≈ base metal mines > Au-Ag mines > Sn-W-Mo-Fe-Mn mines. For parent rock types, similar concentrations were found in the soils derived from sedimentary rocks and metamorphic rocks followed by heterogeneous rocks with igneous and metamorphic processes. Furthermore, farmland soils contained relatively higher Hg levels than paddy soils. Therefore, it can be concluded that soils in Au, Ag, and base metal mines derived from a hydrothermal vein type of metamorphic rocks and pegmatite deposits contained relatively higher concentrations of mercury in the surface environment.

The origin of lead in the organic horizon of tundra soils: Atmospheric deposition, plant translocation from the mineral soil or soil mineral mixing?

International Nuclear Information System (INIS)

Klaminder, Jonatan; Farmer, John G.; MacKenzie, Angus B.

2011-01-01

Knowledge of the anthropogenic contribution to lead (Pb) concentrations in surface soils in high latitude ecosystems is central to our understanding of the extent of atmospheric Pb contamination. In this study, we reconstructed fallout of Pb at a remote sub-arctic region by using two ombrotrophic peat cores and assessed the extent to which this airborne Pb is able to explain the isotopic composition ( 206 Pb/ 207 Pb ratio) in the O-horizon of tundra soils. In the peat cores, long-range atmospheric fallout appeared to be the main source of Pb as indicated by temporal trends that followed the known European pollution history, i.e. accelerated fallout at the onset of industrialization and peak fallout around the 1960s-70s. The Pb isotopic composition of the O-horizon of podzolic tundra soil ( 206 Pb/ 207 Pb = 1.170 ± 0.002; mean ± SD) overlapped with that of the peat ( 206 Pb/ 207 Pb = 1.16 ± 0.01) representing a proxy for atmospheric aerosols, but was clearly different from that of the parent soil material ( 206 Pb/ 207 Pb = 1.22-1.30). This finding indicated that long-range fallout of atmospheric Pb is the main driver of Pb accumulation in podzolic tundra soil. In O-horizons of tundra soil weakly affected by cryoturbation (cryosols) however, the input of Pb from the underlying mineral soil increased as indicated by 206 Pb/ 207 Pb ratios of up to 1.20, a value closer to that of local soil minerals. Nevertheless, atmospheric Pb appeared to be the dominant source in this soil compartment. We conclude that Pb concentrations in the O-horizon of studied tundra soils - despite being much lower than in boreal soils and representative for one of the least exposed sites to atmospheric Pb contaminants in Europe - are mainly controlled by atmospheric inputs from distant anthropogenic sources. - Highlights: → We used Pb isotopic composition to aid interpretation of Pb profiles in tundra soils. → Ombrotrophic peat cores were used as records of atmospheric inputs of Pb. �

Mineral Soil Carbon in Managed Hardwood Forests of the Northeastern US

Science.gov (United States)

Vario, C.; Friedland, A.; Hornig, C.

2013-12-01

New England is characterized by extensive forest cover and large reservoirs of soil carbon (C). In northern hardwood forests, mineral soil C can account for up to 50% of total ecosystem C. There has been an increasing demand for forests to serve both as a C sink and a renewable energy source, and effective management of the ecosystem C balance relies on accurate modeling of each compartment of the ecosystem. However, the dynamics of soil C storage with respect to forest use are variable and poorly understood, particularly in mineral soils. For example, current regional models assume C pools after forest harvesting do not change, while some studies suggest that belowground mineral soil C pools can be affected by disturbances at the soil surface. We quantified mineral soil C pools in previously clear-cut stands in seven research or protected forests across New York, New Hampshire, Massachusetts, and Vermont. The ages of the sites sampled ranged from recently cleared to those with no disturbance history, with 21 forest stands represented in the study. Within each research forest studied, physical parameters such as soil type, forest type, slope and land-use history (aside from forest harvest) did not vary between the stands of different ages. Soil samples were collected to a depth of 60 cm below the mineral-organic boundary using a gas-powered augur and 9.5-cm diameter drill bit. Samples were collected in 10-cm increments in shallow mineral soil and 15-cm increments from 30-60 cm depth. Carbon, nitrogen (N), pH, texture and soil mineralogy were measured across the regional sites. At Bartlett Experimental Forest (BEF) in New Hampshire, mineral soil biogeochemistry in cut and uncut sites was studied at a finer scale. Measurements included soil temperature to 55 cm depth, carbon compound analyses using Py-GCMS and soil microbial messenger RNA extractions from mineral soil. Finally, we simulated C dynamics after harvesting by building a model in Stella, with a particular

The origin of lead in the organic horizon of tundra soils: Atmospheric deposition, plant translocation from the mineral soil or soil mineral mixing?

Energy Technology Data Exchange (ETDEWEB)

Klaminder, Jonatan, E-mail: jonatan.klaminder@emg.umu.se [Department of Ecology and Environmental Science, Umea University, 90187 Umea (Sweden); Farmer, John G. [School of GeoSciences, University of Edinburgh, Edinburgh, EH9 3JN, Scotland (United Kingdom); MacKenzie, Angus B. [Scottish Universities Environmental Research Centre, East Kilbride, G75 0QF, Scotland (United Kingdom)

2011-09-15

Knowledge of the anthropogenic contribution to lead (Pb) concentrations in surface soils in high latitude ecosystems is central to our understanding of the extent of atmospheric Pb contamination. In this study, we reconstructed fallout of Pb at a remote sub-arctic region by using two ombrotrophic peat cores and assessed the extent to which this airborne Pb is able to explain the isotopic composition ({sup 206}Pb/{sup 207}Pb ratio) in the O-horizon of tundra soils. In the peat cores, long-range atmospheric fallout appeared to be the main source of Pb as indicated by temporal trends that followed the known European pollution history, i.e. accelerated fallout at the onset of industrialization and peak fallout around the 1960s-70s. The Pb isotopic composition of the O-horizon of podzolic tundra soil ({sup 206}Pb/{sup 207}Pb = 1.170 {+-} 0.002; mean {+-} SD) overlapped with that of the peat ({sup 206}Pb/{sup 207}Pb = 1.16 {+-} 0.01) representing a proxy for atmospheric aerosols, but was clearly different from that of the parent soil material ({sup 206}Pb/{sup 207}Pb = 1.22-1.30). This finding indicated that long-range fallout of atmospheric Pb is the main driver of Pb accumulation in podzolic tundra soil. In O-horizons of tundra soil weakly affected by cryoturbation (cryosols) however, the input of Pb from the underlying mineral soil increased as indicated by {sup 206}Pb/{sup 207}Pb ratios of up to 1.20, a value closer to that of local soil minerals. Nevertheless, atmospheric Pb appeared to be the dominant source in this soil compartment. We conclude that Pb concentrations in the O-horizon of studied tundra soils - despite being much lower than in boreal soils and representative for one of the least exposed sites to atmospheric Pb contaminants in Europe - are mainly controlled by atmospheric inputs from distant anthropogenic sources. - Highlights: {yields} We used Pb isotopic composition to aid interpretation of Pb profiles in tundra soils. {yields} Ombrotrophic peat

Calcium mineralization in the forest floor and surface soil beneath different tree species in the northeastern US

NARCIS (Netherlands)

Dijkstra, F.A.

2003-01-01

Calcium (Ca) is an important element for neutralizing soil acidity in temperate forests. The immediate availability of Ca in forested acid soils is largely dependent on mineralization of organic Ca, which may differ significantly among tree species. I estimated net Ca mineralization in the forest

Composition of structural fragments and the mineralization rate of organic matter in zonal soils

Science.gov (United States)

Larionova, A. A.; Zolotareva, B. N.; Kolyagin, Yu. G.; Kvitkina, A. K.; Kaganov, V. V.; Kudeyarov, V. N.

2015-10-01

Comparative analysis of the climatic characteristics and the recalcitrance against decomposition of organic matter in the zonal soil series of European Russia, from peat surface-gley tundra soil to brown semidesert soil, has assessed the relationships between the period of biological activity, the content of chemically stable functional groups, and the mineralization of humus. The stability of organic matter has been determined from the ratio of functional groups using the solid-state 13C NMR spectroscopy of soil samples and the direct measurements of organic matter mineralization from CO2 emission. A statistically significant correlation has been found between the period of biological activity and the humification indices: the CHA/CFA ratio, the aromaticity, and the alkyl/ O-alkyl ratio in organic matter. The closest correlation has been observed between the period of biological activity and the alkyl/ O-alkyl ratio; therefore, this parameter can be an important indicator of the soil humus status. A poor correlation between the mineralization rate and the content of chemically stable functional groups in soil organic matter has been revealed for the studied soil series. At the same time, the lowest rate of carbon mineralization has been observed in southern chernozem characterized by the maximum content of aromatic groups (21% Corg) and surface-gley peat tundra soil, where an extremely high content of unsubstituted CH2 and CH3 alkyl groups (41% Corg) has been noted.

Study on adsorption of 60Co in soils and minerals and transportation of 60Co in bean-soil system

International Nuclear Information System (INIS)

Feng Yonghong; Chen Chuanqun; Wang Shouxiang; Zhang Yongxi; Sun Zhiming

1998-02-01

The adsorption and desorption of 60 Co in soils and minerals, and the transportation, accumulation, distribution in bean-soil system are studied. The results are as follows: (1) 60 Co was adsorbed rapidly and desorbed difficultly by soils and minerals. The order of the saturated adsorption rate and K d (distribution coefficient) of 60 Co at the balance value was: kieselguhr>paddy soil (loamy clay)>yellowish red soil>kaoline>perlite>silt-loamy soil. The order of D f (desorption factor) value was: yellowish red soil>silt-loamy soil>kaoline>perlite>paddy soil (loamy clay)>kieselguhr. The dynamic behavior of 60 Co in the soils and minerals could be described as a closed two--compartment model. (2) After 60 Co was introduced to the bean-soil system, the concentration of 60 Co in the root is about 10.4∼23.3 times of that in the stalk, and 30 times of that in the bean pod. The negative correlation between the concentration of 60 Co in the soil and depth was detected, over 90 per cent of 60 Co was retained within 6 centimeters of the surface layer, the half residual depth was 2 centimeters. An opened two-compartment model was applied to describe the behavior of 60 Co in the bean-soil system

Mineralization of 14C-labeled agrochemicals in soil

International Nuclear Information System (INIS)

Xu Bujin; Huang Xiaohua; Hu Xiuqing; Zhang Yongxi

2001-01-01

14 C-labeled compounds were used to study the mineralization of methamidophos, 2,4-D and metsulfuron in soil. Mineralization rate was influenced by the type of soil, concentration of chemical in the soil, the initial soil microbial population and the nature of the chemical. (author)

Competitive sorption between glyphosphate and inorganic phosphate on clay minerals and low organic matter soils

International Nuclear Information System (INIS)

Dion, H.M.; Hill, H.H.Jr.; Washington State Univ., Pullmann, WA; Harsh, J.B.; Washington State Univ., Pullmann, WA

2001-01-01

Inorganic phosphate may influence the adsorption of glyphosate to soil surface sites. It has been postulated that glyphosphate sorption is dominated by the phosphoric acid moiety, therefore, inorganic phosphate could compete with glyphosate for surface sorption sites. Sorption of glyphosate is examined in low organic carbon systems where clay minerals dominate the available adsorption sites using 32 P-labeled phosphate and 14 C-labeled glyphosate to track sorption. Glyphosate sorption was found to be strongly dependent on phosphate additions. Isotherms were generally of the L type, which is consistent with a limited number of surface sites. Most sorption on whole soils could be accounted for by sorption observed on model clays of the same mineral type as found in the soils. (author)

The Interfacial Behavior between Biochar and Soil Minerals and Its Effect on Biochar Stability.

Science.gov (United States)

Yang, Fan; Zhao, Ling; Gao, Bin; Xu, Xiaoyun; Cao, Xinde

2016-03-01

In this study, FeCl3, AlCl3, CaCl2, and kaolinite were selected as model soil minerals and incubated with walnut shell derived biochar for 3 months and the incubated biochar was then separated for the investigation of biochar-mineral interfacial behavior using XRD and SEM-EDS. The XPS, TGA, and H2O2 oxidation were applied to evaluate effects of the interaction on the stability of biochar. Fe8O8(OH)8Cl1.35 and AlCl3·6H2O were newly formed on the biochar surface or inside of the biochar pores. At the biochar-mineral interface, organometallic complexes such as Fe-O-C were generated. All the 4 minerals enhanced the oxidation resistance of biochar surface by decreasing the relative contents of C-O, C═O, and COOH from 36.3% to 16.6-26.5%. Oxidation resistance of entire biochar particles was greatly increased with C losses in H2O2 oxidation decreasing by 13.4-79.6%, and the C recalcitrance index (R50,bicohar) in TGA analysis increasing from 44.6% to 45.9-49.6%. Enhanced oxidation resistance of biochar surface was likely due to the physical isolation from newly formed minerals, while organometallic complex formation was probably responsible for the increase in oxidation resistance of entire biochar particles. Results indicated that mineral-rich soils seemed to be a beneficial environment for biochar since soil minerals could increase biochar stability, which displays an important environmental significance of biochar for long-term carbon sequestration.

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé , Alexander W.; Ohno, Tsutomu; Higgins, Steven R.; Amirbahman, Aria; Yildirim, Nadir; Parr, Thomas B.

2015-01-01

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé, Alexander W.

2015-08-18

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Imaging and Analytical Approaches for Characterization of Soil Mineral Weathering

Energy Technology Data Exchange (ETDEWEB)

Dohnalkova, Alice; Arey, Bruce; Varga, Tamas; Miller, Micah; Kovarik, Libor

2017-07-01

Soil minerals weathering is the primary natural source of nutrients necessary to sustain productivity in terrestrial ecosystems. Soil microbial communities increase soil mineral weathering and mineral-derived nutrient availability through physical and chemical processes. Rhizosphere, the zone immediately surrounding plant roots, is a biogeochemical hotspot with microbial activity, soil organic matter production, mineral weathering, and secondary phase formation all happening in a small temporally ephemeral zone of steep geochemical gradients. The detailed exploration of the micro-scale rhizosphere is essential to our better understanding of large-scale processes in soils, such as nutrient cycling, transport and fate of soil components, microbial-mineral interactions, soil erosion, soil organic matter turnover and its molecular-level characterization, and predictive modeling.

Soil Minerals: AN Overlooked Mediator of Plant-Microbe Competition for Organic Nitrogen in the Rhizosphere

Science.gov (United States)

Grandy, S.; Jilling, A.; Keiluweit, M.

2016-12-01

Recent research on the rate limiting steps in soil nitrogen (N) availability have shifted in focus from mineralization to soil organic matter (SOM) depolymerization. To that end, Schimel and Bennett (2004) argued that together with enzymatic breakdown of polymers to monomers, microsite processes and plant-microbial competition collectively drive N cycling. Here we present new conceptual models arguing that while depolymerization is a critical first step, mineral-organic associations may ultimately regulate the provisioning of bioavailable organic N, especially in the rhizosphere. Mineral-associated organic matter (MAOM) is a rich reservoir for N in soils and often holds 5-7x more N than particulate or labile fractions. However, MAOM is considered largely unavailable to plants as a source of N due to the physicochemical forces on mineral surfaces that stabilize organic matter. We argue that in rhizosphere hotspots, MAOM is in fact a potentially mineralizable and important source of nitrogen for plants. Several biochemical strategies enable plants and microbes to compete with mineral-organic interactions and effectively access MAOM. In particular, root-deposited low molecular weight compounds in the form of root exudates facilitate the biotic and abiotic destabilization and subsequent bioavailability of MAOM. We believe that the competitive balance between the potential fates of assimilable organic N — bound to mineral surfaces or dissolved and available for assimilation — depends on the specific interaction between and properties of the clay, soil solution, mineral-bound organic matter, and microbial community. For this reason, the plant-soil-MAOM interplay is enhanced in rhizosphere hotspots relative to non-rhizosphere environments, and likely strongly regulates plant-microbe competition for N. If these hypotheses are true, we need to reconsider potential soil N cycle responses to changes in climate and land use intensity, focusing on the processes by which

[Organic carbon and carbon mineralization characteristics in nature forestry soil].

Science.gov (United States)

Yang, Tian; Dai, Wei; An, Xiao-Juan; Pang, Huan; Zou, Jian-Mei; Zhang, Rui

2014-03-01

Through field investigation and indoor analysis, the organic carbon content and organic carbon mineralization characteristics of six kinds of natural forest soil were studied, including the pine forests, evergreen broad-leaved forest, deciduous broad-leaved forest, mixed needle leaf and Korean pine and Chinese pine forest. The results showed that the organic carbon content in the forest soil showed trends of gradual decrease with the increase of soil depth; Double exponential equation fitted well with the organic carbon mineralization process in natural forest soil, accurately reflecting the mineralization reaction characteristics of the natural forest soil. Natural forest soil in each layer had the same mineralization reaction trend, but different intensity. Among them, the reaction intensity in the 0-10 cm soil of the Korean pine forest was the highest, and the intensities of mineralization reaction in its lower layers were also significantly higher than those in the same layers of other natural forest soil; comparison of soil mineralization characteristics of the deciduous broad-leaved forest and coniferous and broad-leaved mixed forest found that the differences of litter species had a relatively strong impact on the active organic carbon content in soil, leading to different characteristics of mineralization reaction.

The role of organo-mineral interactions on the capacity of soils to store carbon

Science.gov (United States)

Georgiou, K.; Abramoff, R. Z.; Riley, W. J.; Torn, M. S.

2017-12-01

Observed patterns of soil organic carbon (SOC) content across geochemical regimes are signatures of process and provide opportunities to understand the underlying decomposition and stabilization mechanisms that can guide their representation in models. The type of sorption equation used in soil decomposition models has large implications for both SOC stock and its temperature sensitivity. Here we compared different model formulations of SOC sorption to mineral surfaces, motivated by the myriad of chemical associations between organic and mineral surfaces, and used laboratory and field incubations to inform model parameters. We explored linear, Langmuir, and Freundlich adsorption models, where the latter emerges from heterogeneous compositions of substrate and surface components. We show the effect of model representations on predicted trends of SOC as a function of mineralogy and discuss the role of soil C saturation on emergent patterns. Specifically, our results highlight that the response of mineral-associated (`protected') SOC to changes in plant C inputs depends greatly on the C saturation deficit of the soil and thus, the representation of organo-mineral interactions in models can lead to nonlinear steady-state responses in protected SOC. We also find that, consistent with field experiments, the trend in protected SOC and mineral C saturation capacity is linear, but, interestingly, the slope depends on the degree of C saturation. We contend that this latter finding is an important consideration for field studies that did not find a universal slope and interpreted this as an inability of mineralogy to explain observed patterns. Our results also suggest that warming affects this slope, with higher temperatures causing a decrease in the amount of protected C for a given saturation capacity and C input rate. This means that more C inputs will be needed to keep the same amount of protected C at higher temperatures. Organo-mineral interactions play a key role in

Anaerobic N mineralization in paddy soils in relation to inundation management, physicochemical soil fractions, mineralogy and soil properties

Science.gov (United States)

Sleutel, Steven; Kader, Mohammed Abdul; Ara Begum, Shamim; De Neve, Stefaan

2013-04-01

Anaerobic N mineralization measured from (saturated) repacked soil cores from 25 paddy fields in Bangladesh and was previously found to negatively related to soil N content on a relative basis. This suggests that other factors like soil organic matter (SOM) quality or abiotic factors instead control the anaerobic N mineralization process. We therefore assessed different physical and chemical fractions of SOM, management factors and various soil properties as predictors for the net anaerobic N mineralization. 1° First, we assessed routinely analyzed soil parameters (soil N and soil organic carbon, texture, pH, oxalate- and pyrophosphate-extractable Fe, Al, and Mn, fixed-NH4 content). We found no significant influences of neither soil mineralogy nor the annual length of inundation on soil N mineralization. The anaerobic N mineralization correlated positively with Na-pyrophosphate-extractable Fe and negatively with pH (both at Presistant OM fraction, followed by extraction of mineral bound OM with 10%HF thereby isolating the HF-resistant OM. None of the physicochemical SOM fractions were found useful predictors anaerobic N mineralization. The linkage between these chemical soil N fractions and N supplying processes actually occurring in the soil thus appears to be weak. Regardless, we hypothesize that variation in strength of N-mineral and N-OM linkages is likely to explain variation in bio-availability of organic N and proneness to mineralization. Yet, in order to separate kinetically different soil N fractions we then postulated that an alternative approach would be required, which instead isolates soil N fractions on the basis of bonding strength. In this respect bonding strength should be seen as opposite of proneness to dissolution of released N into water, the habitat of soil microorganisms mediating soil N mineralization. We hypothesize that soil N extracted by water at increasing temperatures would reflect such N fractions with increasing bonding strength, in

Protozoan predation in soil slurries compromises determination of contaminant mineralization potential

International Nuclear Information System (INIS)

Badawi, Nora; Johnsen, Anders R.; Brandt, Kristian K.; Sørensen, Jan; Aamand, Jens

2012-01-01

Soil suspensions (slurries) are commonly used to estimate the potential of soil microbial communities to mineralize organic contaminants. The preparation of soil slurries disrupts soil structure, however, potentially affecting both the bacterial populations and their protozoan predators. We studied the importance of this “slurry effect” on mineralization of the herbicide 2-methyl-4-chlorophenoxyacetic acid (MCPA, 14 C-labelled), focussing on the effects of protozoan predation. Mineralization of MCPA was studied in “intact” soil and soil slurries differing in soil:water ratio, both in the presence and absence of the protozoan activity inhibitor cycloheximide. Protozoan predation inhibited mineralization in dense slurry of subsoil (soil:water ratio 1:3), but only in the most dilute slurry of topsoil (soil:water ratio 1:100). Our results demonstrate that protozoan predation in soil slurries may compromise quantification of contaminant mineralization potential, especially when the initial density of degrader bacteria is low and their growth is controlled by predation during the incubation period. - Highlights: ► We studied the protozoan impact on MCPA mineralization in soil slurries. ► Cycloheximide was used as protozoan inhibitor. ► Protozoa inhibited MCPA mineralization in dilute topsoil slurry and subsoil slurry. ► Mineralization potentials may be underestimated when using soil slurries. - Protozoan predation may strongly bias the quantification of mineralization potential when performed in soil slurries, especially when the initial density of degrader bacteria is low such as in subsoil or very dilute topsoil slurries.

Impact of exotic earthworms on organic carbon sorption on mineral surfaces and soil carbon inventories in a northern hardwood forest

Science.gov (United States)

Amy Lyttle; Kyungsoo Yoo; Cindy Hale; Anthony Aufdenkampe; Stephen D. Sebestyen; Kathryn Resner; Alex. Blum

2015-01-01

Exotic earthworms are invading forests in North America where native earthworms have been absent since the last glaciation. These earthworms bioturbate soils and may enhance physical interactions between minerals and organic matter (OM), thus affecting mineral sorption of carbon (C) which may affect C cycling. We quantitatively show how OM-mineral sorption and soil C...

Mineralogical and geochemical patterns of urban surface soils, the example of Pforzheim, Germany

International Nuclear Information System (INIS)

Norra, Stefan; Lanka-Panditha, Mahesh; Kramar, Utz; Stueben, Doris

2006-01-01

This study presents a combined geochemical and mineralogical survey of urban surface soils. Many studies on urban soils are restricted to purely chemical surveys in order to investigate soil pollution caused by anthropogenic activities such as traffic, heating, industrial processing, waste disposal and many more. In environmental studies, chemical elements are often distinguished as lithogenic and anthropogenic elements. As a novel contribution to those studies, the authors combined the analysis of a broad set of chemical elements with the analysis of the main mineralogical phases. The semi-quantification of mineralogical phases supported the assignment of groups of chemical elements to lithogenic or anthropogenic origin. Minerals are important sinks for toxic elements. Thus, knowledge about their distribution in soils is crucial for the assessment of the environmental hazards due to pollution of urban soils. In Pforzheim, surface soils (0-5 cm depth) from various land use types (forest, agriculture, urban green space, settlement areas of various site densities) overlying different geological units (clastic and chemical sediments) were investigated. Urban surface soils of Pforzheim reflect to a considerable degree the mineral and chemical composition of parent rocks. Irrespective of the parent rocks, elevated concentrations of heavy metals (Zn, Cu, Pb, Sn, Ag) were found in soils throughout the whole inner urban settlement area of Pforzheim indicating pollution. These pollutants will tend to accumulate in inner urban surface soils according to the available adsorption capacity, which is normally higher in soils overlying limestone than in soils overlying sandstone. However, inner urban surface soils overlying sandstone show elevated concentrations of carbonates, phyllo-silicates and Fe and elevated pH values compared with forest soils overlying sandstone. Thus, in comparison to forest soils overlying sandstones, inner urban soils overlying sandstone affected by

Biochar effect on the mineralization of soil organic matter

Directory of Open Access Journals (Sweden)

Sander Bruun

2012-05-01

Full Text Available The objective of this work was to verify whether the addition of biochar to the soil affects the degradation of litter and of soil organic matter (SOM. In order to investigate the effect of biochar on the mineralization of barley straw, soil was incubated with 14C-labelled barley straw with or without unlabelled biochar. To investigate the effect of straw on the mineralization of biochar, soil was incubated with 14C-labelled biochar with or without straw. In addition, to investigate the effect of biochar on old SOM, a soil labelled by applying labelled straw 40 years ago was incubated with different levels of biochar. All experiments had a control treatment, without any soil amendment. The effect of biochar on the straw mineralization was small and nonsignificant. Without biochar, 48±0.2% of the straw carbon was mineralized within the 451 days of the experiment. In comparison, 45±1.6% of C was mineralized after biochar addition of 1.5 g kg-1. In the SOM-labelled soil, the organic matter mineralized more slowly with the increasing doses of biochar. Biochar addition at 7.7 g kg-1 reduced SOM mineralization from 6.6 to 6.3%, during the experimental period. The addition of 15.5 g kg-1 of biochar reduced the mineralized SOM to 5.7%. There is no evidence of increased degradation of either litter or SOM due to biochar addition; consequently, there is no evidence of decreased stability of SOM.

Minerals in soil select distinct bacterial communities in their microhabitats.

Science.gov (United States)

Carson, Jennifer K; Campbell, Louise; Rooney, Deirdre; Clipson, Nicholas; Gleeson, Deirdre B

2009-03-01

We tested the hypothesis that different minerals in soil select distinct bacterial communities in their microhabitats. Mica (M), basalt (B) and rock phosphate (RP) were incubated separately in soil planted with Trifolium subterraneum, Lolium rigidum or left unplanted. After 70 days, the mineral and soil fractions were separated by sieving. Automated ribosomal intergenic spacer analysis was used to determine whether the bacterial community structure was affected by the mineral, fraction and plant treatments. Principal coordinate plots showed clustering of bacterial communities from different fraction and mineral treatments, but not from different plant treatments. Permutational multivariate anova (permanova) showed that the microhabitats of M, B and RP selected bacterial communities different from each other in unplanted and L. rigidum, and in T. subterraneum, bacterial communities from M and B differed (Ppermanova also showed that each mineral fraction selected bacterial communities different from the surrounding soil fraction (P<0.05). This study shows that the structure of bacterial communities in soil is influenced by the mineral substrates in their microhabitat and that minerals in soil play a greater role in bacterial ecology than simply providing an inert matrix for bacterial growth. This study suggests that mineral heterogeneity in soil contributes to the spatial variation in bacterial communities.

Nitrogen stabilization in organo-mineral fractions from soils with different land uses

Science.gov (United States)

Giannetta, Beatrice; Zaccone, Claudio; Rovira, Pere; Vischetti, Costantino; Plaza, César

2017-04-01

Understanding the processes that control quantity and quality of soil organic matter (SOM) interacting with mineral surfaces is of paramount importance. Although several physical fractionation methods have been proposed to date to obtain fractions that mirror SOM degree of stability and protection, a detailed quantification of stabilisation modes through which SOM bounds to the mineral matrix is still lacking. In this research we determined C and N distribution in several soils including coniferous and broadleaved forest soils, grassland soils, technosols and an agricultural soil amended with biochar at rates of 0 and 20 t/ha in a factorial combination with two types of organic amendment (municipal solid waste compost and sewage sludge). We performed a physical size fractionation by ultrasonic dispersion and wet sieving, splitting particles into four different size fractions: coarse sand (2000-200 µm diameter), fine sand (200-50 µm), coarse silt (50-20 µm) and fine silt plus clay (stabilization modes. This method, in fact, allows resolving the nature of different bonds between mineral and organic components by the use of sequential extractions with chemical reagents (potassium sulphate, sodium tetraborate, sodium pyrophosphate, sodium hydroxide, sodium hydroxide after weak acid attack, sodium hydroxide after sodium dithionite pretreatment, and sodium hydroxide after hydrofluoric acid pretreatments). Elemental analysis (CHN) was then carried out on SOM pools isolated from different fractions. Preliminary data show that, for all land uses in general, and for grassland soils in particular, most of the total N is found in organo-mineral complexes (fraction soil N content. Although a small N loss was observed during the fractionation procedure, especially in N-rich samples, and data analysis is still ongoing, these preliminary results could already represent a valuable insight into organic N stabilization by mineral matrix.

Influence of organic surface coatings on the sorption of anticonvulsants on mineral surfaces.

Science.gov (United States)

Qu, Shen; Cwiertny, David M

2013-10-01

Here, we explore the role that sorption to mineral surfaces plays in the fate of two commonly encountered effluent-derived pharmaceuticals, the anticonvulsants phenytoin and carbamazepine. Adsorption isotherms and pH-edge experiments are consistent with electrostatics governing anticonvulsant uptake on metal oxides typically found in soil and aquifer material (e.g., Si, Al, Fe, Mn, and Ti). Appreciable, albeit limited, adsorption was observed only for phenytoin, which is anionic above pH 8.3, on the iron oxides hematite and ferrihydrite. Adsorption increased substantially in the presence of cationic and anionic surfactants, species also commonly encountered in wastewater effluent. For carbamazepine, we propose the enhanced uptake results entirely from hydrophobic interactions with apolar tails of surfactant surface coatings. For phenytoin, adsorption also arises from the ability of surfactants to alter the net charge of the mineral surface and thereby further enhance favorable electrostatic interactions with its anionic form. Collectively, our results demonstrate that although pristine mineral surfaces are likely not major sinks for phenytoin and carbamazepine in the environment, their alteration with organic matter, particularly surfactants, can considerably increase their ability to retain these emerging pollutants in subsurface systems.

Response of Microbial Soil Carbon Mineralization Rates to Oxygen Limitations

Science.gov (United States)

Keiluweit, M.; Denney, A.; Nico, P. S.; Fendorf, S. E.

2014-12-01

The rate of soil organic matter (SOM) mineralization is known to be controlled by climatic factors as well as molecular structure, mineral-organic associations, and physical protection. What remains elusive is to what extent oxygen (O2) limitations impact overall rates of microbial SOM mineralization (oxidation) in soils. Even within upland soils that are aerobic in bulk, factors limiting O2 diffusion such as texture and soil moisture can result in an abundance of anaerobic microsites in the interior of soil aggregates. Variation in ensuing anaerobic respiration pathways can further impact SOM mineralization rates. Using a combination of (first) aggregate model systems and (second) manipulations of intact field samples, we show how limitations on diffusion and carbon bioavailability interact to impose anaerobic conditions and associated respiration constraints on SOM mineralization rates. In model aggregates, we examined how particle size (soil texture) and amount of dissolved organic carbon (bioavailable carbon) affect O2 availability and distribution. Monitoring electron acceptor profiles (O2, NO3-, Mn and Fe) and SOM transformations (dissolved, particulate, mineral-associated pools) across the resulting redox gradients, we then determined the distribution of operative microbial metabolisms and their cumulative impact on SOM mineralization rates. Our results show that anaerobic conditions decrease SOM mineralization rates overall, but those are partially offset by the concurrent increases in SOM bioavailability due to transformations of protective mineral phases. In intact soil aggregates collected from soils varying in texture and SOM content, we mapped the spatial distribution of anaerobic microsites. Optode imaging, microsensor profiling and 3D tomography revealed that soil texture regulates overall O2 availability in aggregate interiors, while particulate SOM in biopores appears to control the fine-scale distribution of anaerobic microsites. Collectively, our

A disconnect between O horizon and mineral soil carbon - Implications for soil C sequestration

Science.gov (United States)

Garten, Charles T., Jr.

2009-03-01

Changing inputs of carbon to soil is one means of potentially increasing carbon sequestration in soils for the purpose of mitigating projected increases in atmospheric CO 2 concentrations. The effect of manipulations of aboveground carbon input on soil carbon storage was tested in a temperate, deciduous forest in east Tennessee, USA. A 4.5-year experiment included exclusion of aboveground litterfall and supplemental litter additions (three times ambient) in an upland and a valley that differed in soil nitrogen availability. The estimated decomposition rate of the carbon stock in the O horizon was greater in the valley than in the upland due to higher litter quality (i.e., lower C/N ratios). Short-term litter exclusion or addition had no effect on carbon stock in the mineral soil, measured to a depth of 30 cm, or the partitioning of carbon in the mineral soil between particulate- and mineral-associated organic matter. A two-compartment model was used to interpret results from the field experiments. Field data and a sensitivity analysis of the model were consistent with little carbon transfer between the O horizon and the mineral soil. Increasing aboveground carbon input does not appear to be an effective means of promoting carbon sequestration in forest soil at the location of the present study because a disconnect exists in carbon dynamics between O horizon and mineral soil. Factors that directly increase inputs to belowground soil carbon, via roots, or reduce decomposition rates of organic matter are more likely to benefit efforts to increase carbon sequestration in forests where carbon dynamics in the O horizon are uncoupled from the mineral soil.

Adsorption of Trametes versicolor laccase to soil iron and aluminum minerals: enzyme activity, kinetics and stability studies.

Science.gov (United States)

Wu, Yue; Jiang, Ying; Jiao, Jiaguo; Liu, Manqiang; Hu, Feng; Griffiths, Bryan S; Li, Huixin

2014-02-01

Laccases play an important role in the degradation of soil phenol or phenol-like substance and can be potentially used in soil remediation through immobilization. Iron and aluminum minerals can adsorb extracellular enzymes in soil environment. In the present study, we investigated the adsorptive interaction of laccase, from the white-rot fungus Trametes versicolor, with soil iron and aluminum minerals and characterized the properties of the enzyme after adsorption to minerals. Results showed that both soil iron and aluminum minerals adsorbed great amount of laccase, independent of the mineral specific surface areas. Adsorbed laccases retained 26-64% of the activity of the free enzyme. Compared to the free laccase, all adsorbed laccases showed higher Km values and lower Vmax values, indicating a reduced enzyme-substrate affinity and a lower rate of substrate conversion in reactions catalyzed by the adsorbed laccase. Adsorbed laccases exhibited increased catalytic activities compared to the free laccase at low pH, implying the suitable application of iron and aluminum mineral-adsorbed T. versicolor laccase in soil bioremediation, especially in acid soils. In terms of the thermal profiles, adsorbed laccases showed decreased thermal stability and higher temperature sensitivity relative to the free laccase. Moreover, adsorption improved the resistance of laccase to proteolysis and extended the lifespan of laccase. Our results implied that adsorbed T. versicolor laccase on soil iron and aluminum minerals had promising potential in soil remediation. Crown Copyright © 2013. Published by Elsevier B.V. All rights reserved.

Geochemical soil sampling for deeply-buried mineralized breccia pipes, northwestern Arizona

Science.gov (United States)

Wenrich, K.J.; Aumente-Modreski, R. M.

1994-01-01

Thousands of solution-collapse breccia pipes crop out in the canyons and on the plateaus of northwestern Arizona; some host high-grade uranium deposits. The mineralized pipes are enriched in Ag, As, Ba, Co, Cu, Mo, Ni, Pb, Sb, Se, V and Zn. These breccia pipes formed as sedimentary strata collapsed into solution caverns within the underlying Mississippian Redwall Limestone. A typical pipe is approximately 100 m (300 ft) in diameter and extends upward from the Redwall Limestone as much as 1000 m (3000 ft). Unmineralized gypsum and limestone collapses rooted in the Lower Permian Kaibab Limestone or Toroweap Formation also occur throughout this area. Hence, development of geochemical tools that can distinguish these unmineralized collapse structures, as well as unmineralized breccia pipes, from mineralized breccia pipes could significantly reduce drilling costs for these orebodies commonly buried 300-360 m (1000-1200 ft) below the plateau surface. Design and interpretation of soil sampling surveys over breccia pipes are plagued with several complications. (1) The plateau-capping Kaibab Limestone and Moenkopi Formation are made up of diverse lithologies. Thus, because different breccia pipes are capped by different lithologies, each pipe needs to be treated as a separate geochemical survey with its own background samples. (2) Ascertaining true background is difficult because of uncertainties in locations of poorly-exposed collapse cones and ring fracture zones that surround the pipes. Soil geochemical surveys were completed on 50 collapse structures, three of which are known mineralized breccia pipes. Each collapse structure was treated as an independent geochemical survey. Geochemical data from each collapse feature were plotted on single-element geochemical maps and processed by multivariate factor analysis. To contrast the results between geochemical surveys (collapse structures), a means of quantifying the anomalousness of elements at each site was developed. This

[Analysis of XRD spectral characteristics of soil clay mineral in two typical cultivated soils].

Science.gov (United States)

Zhang, Zhi-Dan; Luo, Xiang-Li; Jiang, Hai-Chao; Li, Qiao; Shen, Cong-Ying; Liu, Hang; Zhou, Ya-Juan; Zhao, Lan-Po; Wang, Ji-Hong

2014-07-01

The present paper took black soil and chernozem, the typical cultivated soil in major grain producing area of Northeast, as the study object, and determinated the soil particle composition characteristics of two cultivated soils under the same climate and location. Then XRD was used to study the composition and difference of clay mineral in two kinds of soil and the evolutionary mechanism was explored. The results showed that the two kinds of soil particles were composed mainly of the sand, followed by clay and silt. When the particle accumulation rate reached 50%, the central particle size was in the 15-130 microm interval. Except for black soil profile of Shengli Xiang, the content of clay showed converse sequence to the central particle in two soils. Clay accumulated under upper layer (18.82%) in black soil profile while under caliche layer (17.41%) in chernozem profile. Clay content was the least in parent material horizon except in black profile of Quanyanling. Analysis of clay XRD atlas showed that the difference lied in not only the strength of diffraction peak, but also in the mineral composition. The main contents of black soil and chernozem were both 2 : 1 clay, the composition of black soil was smectite/illite mixed layer-illite-vermiculite and that of chernozem was S/I mixture-illite-montmorillonite, and both of them contained little kaolinite, chlorite, quartz and other primary mineral. This paper used XRD to determine the characteristics of clay minerals comprehensively, and analyzed two kinds of typical cultivated soil comparatively, and it was a new perspective of soil minerals study.

Arabian Red Sea coastal soils as potential mineral dust sources

KAUST Repository

Prakash, P. Jish

2016-09-26

Both Moderate Resolution Imaging Spectroradiometer (MODIS) and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) satellite observations suggest that the narrow heterogeneous Red Sea coastal region is a frequent source of airborne dust that, because of its proximity, directly affects the Red Sea and coastal urban centers. The potential of soils to be suspended as airborne mineral dust depends largely on soil texture, moisture content and particle size distributions. Airborne dust inevitably carries the mineralogical and chemical signature of a parent soil. The existing soil databases are too coarse to resolve the small but important coastal region. The purpose of this study is to better characterize the mineralogical, chemical and physical properties of soils from the Arabian Red Sea coastal plain, which in turn will help to improve assessment of dust effects on the Red Sea, land environmental systems and urban centers. Thirteen surface soils from the hot-spot areas of windblown mineral dust along the Red Sea coastal plain were sampled for analysis. Analytical methods included optical microscopy, X-ray diffraction (XRD), inductively coupled plasma optical emission spectrometry (ICP-OES), ion chromatography (IC), scanning electron microscopy (SEM) and laser particle size analysis (LPSA). We found that the Red Sea coastal soils contain major components of quartz and feldspar, as well as lesser but variable amounts of amphibole, pyroxene, carbonate, clays and micas, with traces of gypsum, halite, chlorite, epidote and oxides. The range of minerals in the soil samples was ascribed to the variety of igneous and metamorphic provenance rocks of the Arabian Shield forming the escarpment to the east of the Red Sea coastal plain. The analysis revealed that the samples contain compounds of nitrogen, phosphorus and iron that are essential nutrients to marine life. The analytical results from this study will provide a valuable input into dust emission models used in climate

Lability of soil organic carbon in tropical soils with different clay minerals

DEFF Research Database (Denmark)

Bruun, Thilde Bech; Elberling, Bo; Christensen, Bent Tolstrup

2010-01-01

Soil organic carbon (SOC) storage and turnover is influenced by interactions between organic matter and the mineral soil fraction. However, the influence of clay content and type on SOC turnover rates remains unclear, particularly in tropical soils under natural vegetation. We examined the lability...... of SOC in tropical soils with contrasting clay mineralogy (kaolinite, smectite, allophane and Al-rich chlorite). Soil was sampled from A horizons at six sites in humid tropical areas of Ghana, Malaysian Borneo and the Solomon Islands and separated into fractions above and below 250 µm by wet sieving....... Basal soil respiration rates were determined from bulk soils and soil fractions. Substrate induced respiration rates were determined from soil fractions. SOC lability was significantly influenced by clay mineralogy, but not by clay content when compared across contrasting clay minerals. The lability...

Effects of plant cover on soil N mineralization during the growing season in a sandy soil

Science.gov (United States)

Yao, Y.; Shao, M.; Wei, X.; Fu, X.

2017-12-01

Soil nitrogen (N) mineralization and its availability plays a vital role in regulating ecosystem productivity and C cycling, particularly in semiarid and desertified ecosystems. To determine the effect of plant cover on N turnover in a sandy soil ecosystem, we measured soil N mineralization and inorganic N pools in soil solution during growing season in a sandy soil covered with various plant species (Artemisia desertorum, Salix psammophila, and Caragana korshinskii). A bare sandy soil without any plant was selected as control. Inorganic N pools and N mineralization rates decreased overtime during the growing season, and were not affected by soil depth in bare land soils, but were significantly higher at the 0-10 cm layer than those at the 10-20 cm soil layer under any plant species. Soil inorganic N pool was dominated by ammonium, and N mineralization was dominated by nitrification regardless of soil depth and plant cover. Soils under C. korshinskii have significant higher inorganic N pools and N mineralization rate than soils under bare land and A. desertorum and S. psammophila, and the effects of plant cover were greater at the 0-10 cm soil layer than at the 10-20 cm layer. The effects of C. korshinskii on soil inorganic N pools and mineralization rate varied with the stage of growing season, with greater effects on N pools in the middle growing season, and greater effects on mineralization rate at the last half of the growing season. The results from this study indicate that introduction of C. korshinskii has the potential to increase soil N turnover and availability in sandy soils, and thus to decrease N limitation. Caragana korshinskii is therefore recommend for the remediation of the desertified land.

Formation and development of salt crusts on soil surfaces

KAUST Repository

Dai, Sheng; Shin, Hosung; Santamarina, Carlos

2015-01-01

The salt concentration gradually increases at the soil free surface when the evaporation rate exceeds the diffusive counter transport. Eventually, salt precipitates and crystals form a porous sodium chloride crust with a porosity of 0.43 ± 0.14. After detaching from soils, the salt crust still experiences water condensation and salt deliquescence at the bottom, brine transport across the crust driven by the humidity gradient, and continued air-side precipitation. This transport mechanism allows salt crust migration away from the soil surface at a rate of 5 μm/h forming salt domes above soil surfaces. The surface characteristics of mineral substrates and the evaporation rate affect the morphology and the crystal size of precipitated salt. In particular, substrate hydrophobicity and low evaporation rate suppress salt spreading.

Formation and development of salt crusts on soil surfaces

KAUST Repository

Dai, Sheng

2015-12-14

The salt concentration gradually increases at the soil free surface when the evaporation rate exceeds the diffusive counter transport. Eventually, salt precipitates and crystals form a porous sodium chloride crust with a porosity of 0.43 ± 0.14. After detaching from soils, the salt crust still experiences water condensation and salt deliquescence at the bottom, brine transport across the crust driven by the humidity gradient, and continued air-side precipitation. This transport mechanism allows salt crust migration away from the soil surface at a rate of 5 μm/h forming salt domes above soil surfaces. The surface characteristics of mineral substrates and the evaporation rate affect the morphology and the crystal size of precipitated salt. In particular, substrate hydrophobicity and low evaporation rate suppress salt spreading.

Mineral formation and organo-mineral controls on the bioavailability of carbon at the terrestrial-aquatic interface

Science.gov (United States)

Rod, K. A.; Smith, A. P.; Renslow, R.

2016-12-01

Recent evidence highlights the importance of organo-mineral interactions in regulating the source or sink capacity of soil. High surface area soils, such as allophane-rich or clay-rich soils, retain organic matter (OM) via sorption to mineral surfaces which can also contribute physical isolation in interlayer spaces. Despite the direct correlation between mineral surfaces and OM accumulation, the pedogenic processes controlling the abundance of reactive surface areas and their distribution in the mineral matrix remains unclear. As global soil temperatures rise, the dissolution of primary minerals and formation of new secondary minerals may be thermodynamically favored as part of soil weathering process. Newly formed minerals can supply surfaces for organo-metallic bonding and may, therefore, stabilize OM by surface bonding and physical exclusion. This is especially relevant in environments that intersect terrestrial and aquatic systems, such as the capillary fringe zone in riparian ecosystems. To test the mechanisms of mineral surface area protection of OM, we facilitated secondary precipitation of alumino-silicates in the presence of OM held at two different temperatures in natural Nisqually River sediments (Mt Rainier, WA). This was a three month reaction intended to simulate early pedogenesis. To tease out the influence of mineral surface area increase during pedogenesis, we incubated the sediments at two different soil moisture contents to induce biodegradation. We measured OM desorption, biodegradation, and the molecular composition of mineral-associated OM both prior to and following the temperature manipulation. To simulate the saturation of capillary fringe sediment and associated transport and reaction of OM, column experiments were conducted using the reacted sediments. More co-precipitation was observed in the 20°C solution compared to the 4°C reacted solution suggesting that warming trends alter mineral development and may remove more OM from solution

Influence of iron redox cycling on organo-mineral associations in arctic tundra soils

Science.gov (United States)

Herndon, E.; AlBashaireh, A.; Duroe, K.; Singer, D. M.

2016-12-01

Geochemical interactions between soil organic matter and minerals influence decomposition in many environments but remain poorly understood in arctic tundra systems. In tundra soils that are periodically to persistently saturated, the accumulation of iron oxyhydroxides and organo-iron precipitates at redox interfaces may inhibit decomposition by binding organic molecules and protecting them from microbial degradation. Here, we couple synchrotron-source spectroscopic techniques with chemical sequential extractions and physical density fractionations to evaluate the spatial distribution and speciation of Fe-bearing phases and associated organic matter in organic and mineral horizons of the seasonally thawed active layer in tundra soils from northern Alaska. Mineral-associated organic matter comprised 63 ± 9% of soil organic carbon stored in the active layer of ice wedge polygons. Ferrous iron produced in anoxic mineral horizons diffused upwards and precipitated as poorly-crystalline oxyhydroxides and organic-bound Fe(III) in the organic horizons. Ferrihydrite and goethite were present as coatings on mineral grains and plant debris and in aggregates with clays and particulate organic matter. Organic matter released through acid-dissolution of iron oxides may represent a small pool of readily-degradable organic molecules temporarily stabilized by sorption to iron oxyhydroxide surfaces, while larger quantities of particulate organic carbon and humic-like substances may be physically protected from decomposition by Fe-oxide coatings and aggregation. We conclude that formation of poorly-crystalline and crystalline iron oxides at redox interfaces contributes to mineral protection of organic matter through sorption, aggregation, and co-precipitation reactions. Further study of organo-mineral associations is necessary to determine the net impact of mineral-stabilization on carbon storage in rapidly warming arctic ecosystems.

Effect of aluminium on dissolved organic matter mineralization in an allophanic and kaolinitic temperate rain forest soil

Science.gov (United States)

Merino, Carolina; Matus, Francisco; Fontaine, Sebastien

2016-04-01

Aluminium (Al) and it influence on the mineralization of dissolved organic matter (DOM) and thus on carbon (C) sequestration in forest soils is poorly understood. We hypothesized that an addition of Al to the soil solution beyond a molar Al:C ratio of 0.1, induces precipitation of the organic matter which leads to an excess Al in the soil solution causing an inhibitory effect for growing microorganisms. We investigated the effect of Al concentrations for the potential of C biodegradation at different Al:C ratios from DOM and Ah mineral soil horizons from two temperate rain forest soils from southern Chile. Dissolved organic matter and surface mineral horizons were incubated with initial molar Al:C ratio from 0.08 to 1.38 found under at field conditions. Mineralization was quantified by measurement of C-CO2 evolved during 15 days. Increasing the initial Al:C ratio > 0.12, led to a considerable reduction in mineralization (up to 70%). For Al:C ratio biodegradation of DOM and thus an increased in the C sequestration in mineral soils with molar Al:C ratio > 0.12. The observed DOM losses in the stream water of pristine southern forests can be explained by increasing the bioavailability of organic C for Al:C ratio < 0.12. Aluminium concentration had a marked effect at the spectral ART-FTIR bands assigned to cellulose-like and aromatic compounds in Ah mineral soil, diminishing the mineralization. The present results were also confirmed by the Al fluorescence using a confocal microscopy.

Overcoming soil compaction in surface mine reclamation

Energy Technology Data Exchange (ETDEWEB)

Sweigard, R.J. (University of Kentucky, Lexington, KY (USA). Dept. of Mining Engineering)

1991-01-01

Rubber-tyred soil reconstruction equipment causes compaction of soil and means surface mine operators cannot satisfy crop yield standards defined by the Surface Mining Control and Reclamation Act. Soil compaction can be overcome by either modifying the reconstruction process or alleviating the problem, for example by deep tillage, once it occurs. The Dept. of Mining Engineering at the Institute of Mining and Minerals Research is conducting a laboratory investigation into a method of injecting low density porous organic material into a bin containing soil at the same time as the soil is ripped. This should prevent voids collapsing when subjected to forces from farm equipment and natural sources. Soil analyses are performed before and after the injection. Ripping and injection with ground pecan shells had a residual effect on nuclear bulk density compared to the initially compacted case and also showed an improvement in hydraulic conductivity. Work is in progress on modifying the system to handle other injection material and should lead on to field tests on a prototype involving both soil analysis and crop yield determination. 1 fig.

Overcoming soil compaction in surface mine reclamation

International Nuclear Information System (INIS)

Sweigard, R.J.

1991-01-01

Rubber-tyred soil reconstruction equipment causes compaction of soil and means surface mine operators cannot satisfy crop yield standards defined by the Surface Mining Control and Reclamation Act. Soil compaction can be overcome by either modifying the reconstruction process or alleviating the problem, for example by deep tillage, once it occurs. The Dept. of Mining Engineering at the Institute of Mining and Minerals Research is conducting a laboratory investigation into a method of injecting low density porous organic material into a bin containing soil at the same time as the soil is ripped. This should prevent voids collapsing when subjected to forces from farm equipment and natural sources. Soil analyses are performed before and after the injection. Ripping and injection with ground pecan shells had a residual effect on nuclear bulk density compared to the initially compacted case and also showed an improvement in hydraulic conductivity. Work is in progress on modifying the system to handle other injection material and should lead on to field tests on a prototype involving both soil analysis and crop yield determination. 1 fig

Dissolved organic carbon from sewage sludge and manure can affect estrogen sorption and mineralization in soils

International Nuclear Information System (INIS)

Stumpe, Britta; Marschner, Bernd

2010-01-01

In this study, effects of sewage sludge and manure borne dissolved organic carbon (DOC) on 17β-estradiol (E2) and 17α-ethinylestradiol (EE2) sorption and mineralization processes were investigated in three agricultural soils. Batch equilibrium techniques and equilibrium dialysis methods were used to determine sorption mechanisms between DOC, estrogens and the soil solid phase. It was found that that the presence of organic waste borne DOC decreased estrogen sorption in soils which seems to be controlled by DOC/estrogen complexes in solution and by exchange processes between organic waste derived and soil borne DOC. Incubation studies performed with 14 C-estrogens showed that DOC addition decreased estrogen mineralization, probably due to reduced bioavailability of estrogens associated with DOC. This increased persistence combined with higher mobility could increase the risk of estrogen transport to ground and surface waters. - The effect of DOC on estrogen sorption and mineralization is influenced by exchange processes between organic waste borne and soil derived DOC.

Dissolved organic carbon from sewage sludge and manure can affect estrogen sorption and mineralization in soils

Energy Technology Data Exchange (ETDEWEB)

Stumpe, Britta, E-mail: britta.stumpe@rub.d [Ruhr-University Bochum, Institute of Geography, Department Soil Science/Soil Ecology, Universitaetsstr. 150, 44780 Bochum (Germany); Marschner, Bernd, E-mail: bernd.marschner@rub.d [Ruhr-University Bochum, Institute of Geography, Department Soil Science/Soil Ecology, Universitaetsstr. 150, 44780 Bochum (Germany)

2010-01-15

In this study, effects of sewage sludge and manure borne dissolved organic carbon (DOC) on 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) sorption and mineralization processes were investigated in three agricultural soils. Batch equilibrium techniques and equilibrium dialysis methods were used to determine sorption mechanisms between DOC, estrogens and the soil solid phase. It was found that that the presence of organic waste borne DOC decreased estrogen sorption in soils which seems to be controlled by DOC/estrogen complexes in solution and by exchange processes between organic waste derived and soil borne DOC. Incubation studies performed with {sup 14}C-estrogens showed that DOC addition decreased estrogen mineralization, probably due to reduced bioavailability of estrogens associated with DOC. This increased persistence combined with higher mobility could increase the risk of estrogen transport to ground and surface waters. - The effect of DOC on estrogen sorption and mineralization is influenced by exchange processes between organic waste borne and soil derived DOC.

[Response of mineralization of dissolved organic carbon to soil moisture in paddy and upland soils in hilly red soil region].

Science.gov (United States)

Chen, Xiang-Bi; Wang, Ai-Hua; Hu, Le-Ning; Huang, Yuan; Li, Yang; He, Xun-Yang; Su, Yi-Rong

2014-03-01

Typical paddy and upland soils were collected from a hilly subtropical red-soil region. 14C-labeled dissolved organic carbon (14C-DOC) was extracted from the paddy and upland soils incorporated with 14C-labeled straw after a 30-day (d) incubation period under simulated field conditions. A 100-d incubation experiment (25 degrees C) with the addition of 14C-DOC to paddy and upland soils was conducted to monitor the dynamics of 14C-DOC mineralization under different soil moisture conditions [45%, 60%, 75%, 90%, and 105% of the field water holding capacity (WHC)]. The results showed that after 100 days, 28.7%-61.4% of the labeled DOC in the two types of soils was mineralized to CO2. The mineralization rates of DOC in the paddy soils were significantly higher than in the upland soils under all soil moisture conditions, owing to the less complex composition of DOC in the paddy soils. The aerobic condition was beneficial for DOC mineralization in both soils, and the anaerobic condition was beneficial for DOC accumulation. The biodegradability and the proportion of the labile fraction of the added DOC increased with the increase of soil moisture (45% -90% WHC). Within 100 days, the labile DOC fraction accounted for 80.5%-91.1% (paddy soil) and 66.3%-72.4% (upland soil) of the cumulative mineralization of DOC, implying that the biodegradation rate of DOC was controlled by the percentage of labile DOC fraction.

Sorption and Transport of Pharmaceutical chemicals in Organic- and Mineral-rich Soils

Science.gov (United States)

Vulava, V. M.; Schwindaman, J.; Murphey, V.; Kuzma, S.; Cory, W.

2011-12-01

Pharmaceutical, active ingredients in personal care products (PhACs), and their derivative compounds are increasingly ubiquitous in surface waters across the world. Sorption and transport of four relatively common PhACs (naproxen, ibuprofen, cetirizine, and triclosan) in different natural soils was measured. All of these compounds are relatively hydrophobic (log KOW>2) and have acid/base functional groups, including one compound that is zwitterionic (cetirizine.) The main goal of this study was to correlate organic matter (OM) and clay content in natural soils and sediment with sorption and degradation of PhACs and ultimately their potential for transport within the subsurface environment. A- and B-horizon soils were collected from four sub-regions within a pristine managed forested watershed near Charleston, SC, with no apparent sources of anthropogenic contamination. These four soil series had varying OM content (fOC) between 0.4-9%, clay mineral content between 6-20%, and soil pH between 4.5-6. The A-horizon soils had higher fOC and lower clay content than the B-horizon soils. Sorption isotherms measured from batch sorption experimental data indicated a non-linear sorption relationship in all A- and B-horizon soils - stronger sorption was observed at lower PhAC concentrations and lower sorption at higher concentrations. Three PhACs (naproxen, ibuprofen, and triclosan) sorbed more strongly with higher fOC A-horizon soils compared with the B-horizon soils. These results show that soil OM had a significant role in strongly binding these three PhACs, which had the highest KOW values. In contrast, cetirizine, which is predominantly positively charged at pH below 8, strongly sorbed to soils with higher clay mineral content and least strongly to higher fOC soils. All sorption isotherms fitted well to the Freundlich model. For naproxen, ibuprofen, and triclosan, there was a strong and positive linear correlation between the Freundlich adsorption constant, Kf, and f

Arabian Red Sea coastal soils as potential mineral dust sources

Directory of Open Access Journals (Sweden)

P. Jish Prakash

2016-09-01

Full Text Available Both Moderate Resolution Imaging Spectroradiometer (MODIS and Spinning Enhanced Visible and InfraRed Imager (SEVIRI satellite observations suggest that the narrow heterogeneous Red Sea coastal region is a frequent source of airborne dust that, because of its proximity, directly affects the Red Sea and coastal urban centers. The potential of soils to be suspended as airborne mineral dust depends largely on soil texture, moisture content and particle size distributions. Airborne dust inevitably carries the mineralogical and chemical signature of a parent soil. The existing soil databases are too coarse to resolve the small but important coastal region. The purpose of this study is to better characterize the mineralogical, chemical and physical properties of soils from the Arabian Red Sea coastal plain, which in turn will help to improve assessment of dust effects on the Red Sea, land environmental systems and urban centers. Thirteen surface soils from the hot-spot areas of windblown mineral dust along the Red Sea coastal plain were sampled for analysis. Analytical methods included optical microscopy, X-ray diffraction (XRD, inductively coupled plasma optical emission spectrometry (ICP-OES, ion chromatography (IC, scanning electron microscopy (SEM and laser particle size analysis (LPSA. We found that the Red Sea coastal soils contain major components of quartz and feldspar, as well as lesser but variable amounts of amphibole, pyroxene, carbonate, clays and micas, with traces of gypsum, halite, chlorite, epidote and oxides. The range of minerals in the soil samples was ascribed to the variety of igneous and metamorphic provenance rocks of the Arabian Shield forming the escarpment to the east of the Red Sea coastal plain. The analysis revealed that the samples contain compounds of nitrogen, phosphorus and iron that are essential nutrients to marine life. The analytical results from this study will provide a valuable input into dust emission models

Basic exchangeable cations in Finnish mineral soils

Directory of Open Access Journals (Sweden)

Armi Kaila

1972-09-01

Full Text Available The content of exchangeable Ca, Mg, K and Na replaced by neutral ammonium acetate was determined in 470 samples of mineral soils from various parts of Finland, except from Lapland. The amount of all these cations tended to increase with an increase in the clay content, but variation within each textural class was large, and the ranges usually overlapped those of the other classes. The higher acidity of virgin surface soils was connected with a lower average degree of saturation by Ca as compared with the corresponding textural classes of cultivated soils. No significant difference in the respective contents of other cations was detected. The samples of various textural groups from deeper layers were usually poorer in exchangeable Ca and K than the corresponding groups of plough layer. The mean content of exchangeable Mg was equal or even higher in the samples from deeper layers than in the samples from plough layer, except in the group of sand soils. The percentage of Mg of the effective CEC increased, as an average, from 9 in the sand and fine sand soils of plough layer to 30 in the heavy clay soils; in the heavy clay soils from deeper layers its mean value was 38 ± 4 %. In the samples of plough layer, the mean ratio of Ca to Mg in sand and fine sand soils was about 9, in silt and loam soils about 6, in the coarser clay soils about 4, and in heavy clay about 2.

Qualitative soil mineral analysis by EDXRF, XRD and AAS probes

International Nuclear Information System (INIS)

Singh, Virendra; Agrawal, H.M.

2012-01-01

Soil minerals study is vital in terms of investigating the major soil forming compounds and to find out the fate of minor and trace elements, essential for the soil–plant interaction purpose. X-ray diffraction (XRD) has been a popular technique to search out the phases for different types of samples. For the soil samples, however, employing XRD is not so straightforward due to many practical problems. In the current approach, principal component analysis (PCA) has been used to have an idea of the minerals present, in qualitative manner, in the soil under study. PCA was used on the elemental concentrations data of 17 elements, determined by the energy dispersive X-ray fluorescence (EDXRF) technique. XRD analysis of soil samples has been done also to identify the minerals of major elements. Some prior treatments, like removal of silica by polytetrafluoroethylene (PTFE) slurry and grinding with alcohol, were given to samples to overcome the peak overlapping problems and to attain fine particle size which is important to minimize micro-absorption corrections, to give reproducible peak intensities and to minimize preferred orientation. A 2θ step of 0.05°/min and a longer dwell time than normal were used to reduce interferences from background noise and to increase the counting statistics. Finally, the sequential extraction procedure for metal speciation study has been applied on soil samples. Atomic absorption spectroscopy (AAS) was used to find the concentrations of metal fractions bound to various forms. Applying all the three probes, the minerals in the soils can be studied and identified, successfully. - Highlights: ► Qualitative soil minerals analysis by EDXRF, AAS and XRD methods. ► There is a requirement of other means and methods due to inadequacy of XRD. ► Principal component analysis (PCA) provides an idea of minerals present in soil. ► Trace elements complexes can be determined by AAS probe. ► EDXRF, AAS and XRD, in combination, enable

Aided Phytostabilization of Copper Contaminated Soils with L. Perenne and Mineral Sorbents as Soil Amendments

Science.gov (United States)

Radziemska, Maja

2017-09-01

The present study was designed to assess phytostabilization strategies for the treatment of soil co-contaminated by increasing levels of copper with the application mineral amendments (chalcedonite, zeolite, dolomite). From the results it will be possible to further elucidate the benefits or potential risks derived from the application of different types of mineral amendments in the remediation of a copper contaminated soil. A glasshouse pot experiment was designed to evaluate the potential use of different amendments as immobilizing agents in the aided phytostabilization of Cu-contaminated soil using ryegrass (Lolium perenne L.). The content of trace elements in plants and total in soil, were determined using the method of spectrophotometry. All of the investigated element contents in the tested parts of L. perenne were significantly different in the case of applying mineral amendments to the soil, as well as increasing concentrations of copper. The greatest average above-ground biomass was observed for soil amended with chalcedonite. In this experiment, all analyzed metals accumulated predominantly in the roots of the tested plant. In general, applying mineral amendments to soil contributed to decreased levels of copper concentrations.

Can Biochar Protect Labile Organic Matter Against Mineralization in Soil?

Institute of Scientific and Technical Information of China (English)

Giovanna B.MELAS; Oriol ORTIZ; Josep M.ALACA(N)IZ

2017-01-01

Biochar could help to stabilize soil organic (SOM) matter,thus sequestering carbon (C) into the soil.The aim of this work was to determine an easy method i) to estimate the effects of the addition of biochar and nutrients on the organic matter (SOM)mineralization in an artificial soil,proposed by the Organization for Economic Co-operation and Development (OECD),amended with glucose and ii) to measure the amount of labile organic matter (glucose) that can be sorbed and thus be partially protected in the same soil,amended or not amended with biochar.A factorial experiment was designed to check the effects of three single factors (biochar,nutrients,and glucose) and their interactions on whole SOM mineralization.Soil samples were inoculated with a microbial inoculum and preincubated to ensure that their biological activities were not limited by a small amount of microbial biomass,and then they were incubated in the dark at 21 ℃ for 619 d.Periodical measurements of C mineralized to carbon dioxide (CO2) were carried out throughout the 619-d incubation to allow the mineralization of both active and slow organic matter pools.The amount of sorbed glucose was calculated as the difference between the total and remaining amounts of glucose added in a soil extract.Two different models,the Freundlich and Langmuir models,were selected to assess the equilibrium isotherms of glucose sorption.The CO2-C release strongly depended on the presence of nutrients only when no biochar was added to the soil.The mineralization of organic matter in the soil amended with both biochar and glucose was equal to the sum of the mineralization of the two C sources separately.Furthermore,a significant amount of glucose can be sorbed on the biochar-amended soil,suggesting the involvement of physico-chemical mechanisms in labile organic matter protection.

Soil Surface Organic Layers in Alaska's Arctic Foothills: Development, Distribution and Microclimatic Feedbacks

Science.gov (United States)

Baughman, C. A.; Mann, D. H.; Verbyla, D.; Valentine, D.; Kunz, M. L.; Heiser, P. A.

2013-12-01

Accumulated organic matter at the ground surface plays an important role in arctic ecosystems. These soil surface organic layers (SSOLs) influence temperature, moisture, and chemistry in the underlying mineral soil and, on a global basis, comprise enormous stores of labile carbon. Understanding the dynamics of SSOLs is prerequisite to modeling the responses of arctic ecosystem processes to climate changes. Here, we ask three questions regarding SSOLs in the Arctic Foothills in northern Alaska: 1) What environmental factors control their spatial distribution? 2) How long do they take to form? 3) What is the relationship between SSOL thickness and mineral soil temperature through the growing season? The best topographically-controlled predictors of SSOL thickness and spatial distribution are duration of sunlight during the growing-season, upslope drainage area, slope gradient, and elevation. SSOLs begin to form within several decades following disturbance but require 500-700 years to reach equilibrium states. Once formed, mature SSOLs lower peak growing-season temperature and mean annual temperature in the underlying mineral horizon by 8° and 3° C respectively, which reduces available growing degree days within the upper mineral soil by nearly 80%. How ongoing climate change in northern Alaska will affect the region's SSOLs is an open and potentially crucial question.

Modelling soil organic carbon concentration of mineral soils in arable lands using legacy soil data

DEFF Research Database (Denmark)

Suuster, E; Ritz, Christian; Roostalu, H

2012-01-01

is appropriate if the study design has a hierarchical structure as in our scenario. We used the Estonian National Soil Monitoring data on arable lands to predict SOC concentrations of mineral soils. Subsequently, the model with the best prediction accuracy was applied to the Estonian digital soil map...

Influence of iron redox cycling on organo-mineral associations in Arctic tundra soil

Science.gov (United States)

Herndon, Elizabeth; AlBashaireh, Amineh; Singer, David; Roy Chowdhury, Taniya; Gu, Baohua; Graham, David

2017-06-01

carbon in the organic horizons (28 ± 5 wt.% C) were approximately twice the concentrations in the mineral horizons (14 ± 2 wt.% C), and organic matter was dominated by base-extractable and insoluble organics enriched in aromatic and aliphatic moieties. Conversely, water-soluble organic molecules and organics solubilized through acid-dissolution of iron oxides comprised soil organic C and were consistent with a mixture of alcohols, sugars, and small molecular weight organic acids and aromatics released through decomposition of larger molecules. Integrated over the entire depth of the active layer, soils contained 11 ± 4 kg m-2 low-density, particulate organic C and 19 ± 6 kg m-2 high-density, mineral-associated organic C, indicating that 63 ± 19% of organic C in the active layer was associated with the mineral fraction. We conclude that organic horizons were enriched in poorly crystalline and crystalline iron oxide phases derived from upward translocation of dissolved Fe(II) and Fe(III) from mineral horizons. Precipitation of iron oxides at the redox interface has the potential to contribute to mineral protection of organic matter and increase the residence time of organic carbon in arctic soils. Our results suggest that iron oxides may inhibit organic carbon degradation by binding low-molecular-weight organic compounds, stabilizing soil aggregates, and forming thick coatings around particulate organic matter. Organic matter released through acid-dissolution of iron oxides could represent a small pool of readily-degradable organic molecules temporarily stabilized by sorption to iron oxyhydroxide surfaces. The distribution of iron in organic complexes and inorganic phases throughout the soil column constrains Fe(III) availability to anaerobic iron-reducing microorganisms that oxidize organic matter to produce CO2 and CH4 in these anoxic environments. Future predictions of carbon storage and respiration in the arctic tundra should consider such influences of mineral

Organic matter dynamics and N mineralization in grassland soils

NARCIS (Netherlands)

Hassink, J.

1995-01-01

The aims of this study are i) to improve our understanding of the interactions between soil texturelsoil structure, soil organic matter, soil biota and mineralization in grassland soils, ii) to develop a procedure that yields soil organic matter fractions that can be determined directly

Mineralization of polycyclic and n-heterocyclic aromatic compounds in hydrocarbon-contaminated soils

International Nuclear Information System (INIS)

Grosser, R.J.; Warshawsky, D.; Vestal, J.R.

1995-01-01

The comparative mineralization of eight polycyclic aromatic compounds in five soils collected from an abandoned coal tar refinery in eastern Ohio was determined. The soils showed differences only in total extractable hydrocarbon content of the soil chemical characteristics measured. The compounds studied included five polycyclic aromatic hydrocarbons (phenanthrene, anthracene, pyrene, and carcinogenic benz[a]anthracene and benzo[a]pyrene) and three N-heterocyclic aromatics (9H-carbazole, and carcinogenic 7H-dibenzo[c,g]carbazole and dibenz[a,j]acridine). Mineralization was measured by serum bottle radiorespirometry. Only phenanthrene, anthracene, pyrene, benz[a]anthracene, and carbazole were mineralized in the soils after 64 d. Two of the soils with eight to 15 times the hexane -extractable hydrocarbon content consistently showed more rapid initial rates and higher overall extents of mineralization compared to the other three soils. Overall extents of mineralization ranged from 38 to 55% for phenanthrene, 10 to 60% for anthracene, 25 to 70% for pyrene, background to 40% for benz[a]anthracene, and 25 to 50% for carbazole after 64 d. Extents of mineralization by indigenous soil microbiota appear to be more dependent on the chemical characteristics of the soil and not soil total biomass and activity. Cultures capable of degrading phenanthrene, anthracene, and pyrene were obtained following enrichment techniques. A Mycobacterium sp. capable of degrading these three compounds was isolated and reintroduced into two of the soils, resulting in mineralization enhanced above that of the indigenous soil microbial population. These data indicate that the future success of bioremediation methods relies on the characterization of environmental parameters affecting microbial degradation as well as the isolation of microbial populations that can reduce toxicity in the environment

Root-driven Weathering Impacts on Mineral-Organic Associations in Deep Soil

Science.gov (United States)

Keiluweit, M.; Garcia Arredondo, M.; Tfaily, M. M.; Kukkadapu, R. K.; Schulz, M. S.; Lawrence, C. R.

2017-12-01

Plant roots dramatically reshape the soil environments through the release of organic compounds. While root-derived organic compounds are recognized as an important source of soil C, their role in promoting weathering reactions has largely been overlooked. On the one hand, root-driven weathering may generate mineral-organic associations, which can protect soil C for centuries to millennia. On the other hand, root-driven weathering also transforms minerals, potentially disrupting protective mineral-organic associations in the process. Hence root-derived C may not only initiate C accumulation, but also diminish C stocks through disruption of mineral-organic associations. Here we determined the impact of rhizogenic weathering on mineral-organic associations, and associated changes in C storage, across the Santa Cruz Marine Terrace chronosequence (65ka-226ka). Using a combination of high-resolution mass spectrometry, Mössbauer, and X-ray (micro)spectroscopy, we examined mineral-organic associations of deep soil horizons characterized by intense rhizogenic weathering gradients. Initial rhizogenic weathering dramatically increased C stocks, which is directly linked to an increase of microbially-derived C bound to monomeric Fe and Al and nano-goethite. As weathering proceeded, the soil C stocks declined concurrent with an increasingly plant-derived C signature and decreasing crystallinity. X-ray spectromicroscopic analyses revealed strong spatial associations between C and Fe during initial weathering stages, indicative of protective mineral-organic associations. In contrast, later weathering stages showed weaker spatial relationships between C and Fe. We conclude that rhizogenic weathering enhance C storage by creating protective mineral-organic associations in the initial weathering stages. As root-driven weathering proceeds, minerals are transformed into more crystalline phases that retain lower amounts of C. Our results demonstrate that root-induced weathering

Magnetic minerals in soils across the forest-prairie ecotone in NW Minnesota

Science.gov (United States)

Maxbauer, D.; Feinberg, J. M.; Fox, D. L.; Nater, E. A.

2016-12-01

Soil pedogenesis results in a complex assemblage of iron oxide minerals that can be disentangled successfully using sensitive magnetic techniques to better delineate specific soil processes. Here, we evaluate the variability in soil processes within forest, prairie, and transitional soils along an 11 km transect of anthropogenically unaltered soils that span the forest-to-prairie ecotone in NW Minnesota. All soils in this study developed on relatively uniform topography, similar glacial till parent material, under a uniform climate, and presumably over similar time intervals. The forest-to-prairie transition zone in this region is controlled by naturally occurring fires, affording the opportunity to evaluate differences in soil processes related to vegetation (forest versus prairie) and burning (prairie and transitional soils). Results suggest that the pedeogenic fraction of magnetite/maghemite in soils is similar in all specimens and is independent of soil type, vegetation, and any effects of burning. Magnetically enhanced horizons have 45% of remanence held by a low-coercivity pedogenic component (likely magnetite/maghemite) regardless of vegetation cover and soil type. Enhancement ratios for magnetic susceptibility and low-field remanences, often used as indicators of pedogenic magnetic minerals, are more variable but remain statistically equivalent across the transect. These results support the hypothesis that pedogenic magnetic minerals in soils mostly reflect ambient climatic conditions regardless of the variability in soil processes related to vegetation and soil type. The non-pedogenic magnetic mineral assemblage shows clear distinctions between the forest, prairie, and transitional soils in hysteresis properties (remanence and coercivity ratios; Mr/Ms and Bc/Bcr, respectively), suggesting that variable processes in these settings influence the local magnetic mineral assemblage, and that it may be possible to use magnetic minerals in paleosols to constrain

The impact of mineral composition on compressibility of saturated soils

OpenAIRE

Dolinar, Bojana

2012-01-01

This article analyses the impact of soils` mineral composition on their compressibility. Physical and chemical properties of minerals which influence the quantity of intergrain water in soils and, consequently, the compressibility of soils are established by considering the previous theoretical findings. Test results obtained on artificially prepared samples are used to determine the analytical relationship between the water content and stress state, depending on the mineralogical properties ...

Spatial variation in microbial processes controlling carbon mineralization within soils and sediments

Energy Technology Data Exchange (ETDEWEB)

Fendorf, Scott [Stanford Univ., CA (United States); Kleber, Markus [Oregon State Univ., Corvallis, OR (United States); Nico, Peter [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)

2017-10-19

Soils have a defining role in global carbon cycling, having one of the largest dynamic stocks of C on earth—3300 Pg of C are stored in soils, which is three-times the amount stored in the atmosphere and more than the terrestrial land plants. An important control on soil organic matter (SOM) quantities is the mineralization rate. It is well recognized that the rate and extent of SOM mineralization is affected by climatic factors and mineral-organic matter associations. What remained elusive is to what extent constraints on microbial metabolism induced by the respiratory pathway, and specifically the electron acceptor in respiration, control overall rates of carbon mineralization in soils. Therefore, physical factors limiting oxygen diffusion such as soil texture and aggregate size (soil structure) may therefore be central controls on C mineralization rates. The goal of our research was therefore to determine if variations in microbial metabolic rates induced by anaerobic microsites in soils are a major control on SOM mineralization rates and thus storage. We performed a combination of laboratory experiments and field investigations will be performed to fulfill our research objectives. We used laboratory studies to examine fundamental factors of respiratory constraints (i.e., electron acceptor) on organic matter mineralization rates. We ground our laboratory studies with both manipulation of field samples and in-field measurements. Selection of the field sites is guided by variation in soil texture and structure while having (other environmental/soil factors constant. Our laboratory studies defined redox gradients and variations in microbial metabolism operating at the aggregate-scale (cm-scale) within soils using a novel constructed diffusion reactor. We further examined micro-scale variation in terminal electron accepting processes and resulting C mineralization rates within re-packed soils. A major outcome of our research is the ability to quantitatively place

Depth distribution of 137Cs adsorption property of clay minerals influenced by mineral weathering

International Nuclear Information System (INIS)

Nakao, Atsushi; Funakawa, Shinya; Kosaki, Takashi

2007-01-01

Radiocesium adsorption potential of mica clay mineral can increase as it is weathered, because K depletion in mica interlayer sites generates new Cs selective sites. However, in soils weathered under field conditions, the increase in 137 Cs adsorption potential associated with mineral weathering has not been observed extensively. We investigated four soil profiles from Japan and Thailand with different soil pH ranges (3.3-4.0, 4.2-4.3, 5.0-5.7, and 5.5-7.3). The solid/liquid distribution coefficients of Cs ( Cs Kd) in clay ( 137 Cs adsorption potential of mica clay minerals. In three soil profiles, Cs Kd value in clay was the largest at a surface horizon and was decreased with depth, whereas in the most acidic of Podzolic soil profile, it was the largest at B horizon. The large Cs Kd value in surface clays relative to deeper horizons were well associated with that of 2.0-1.0 μm clay fraction. We assumed that the 137 Cs adsorption potential increased at surface horizons mainly because coarser clay micas were weathered and generated Cs selective sites. The exceptional result obtained in Podzolic soil profile suggests that too intensive weathering destruct mica structure and may decrease in Cs adsorption potential of mica clay minerals. (author)

Temperature response of permafrost soil carbon is attenuated by mineral protection.

Science.gov (United States)

Gentsch, Norman; Wild, Birgit; Mikutta, Robert; Čapek, Petr; Diáková, Katka; Schrumpf, Marion; Turner, Stephanie; Minnich, Cynthia; Schaarschmidt, Frank; Shibistova, Olga; Schnecker, Jörg; Urich, Tim; Gittel, Antje; Šantrůčková, Hana; Bárta, Jiři; Lashchinskiy, Nikolay; Fuß, Roland; Richter, Andreas; Guggenberger, Georg

2018-05-18

Climate change in Arctic ecosystems fosters permafrost thaw and makes massive amounts of ancient soil organic carbon (OC) available to microbial breakdown. However, fractions of the organic matter (OM) may be protected from rapid decomposition by their association with minerals. Little is known about the effects of mineral-organic associations (MOA) on the microbial accessibility of OM in permafrost soils and it is not clear which factors control its temperature sensitivity. In order to investigate if and how permafrost soil OC turnover is affected by mineral controls, the heavy fraction (HF) representing mostly MOA was obtained by density fractionation from 27 permafrost soil profiles of the Siberian Arctic. In parallel laboratory incubations, the unfractionated soils (bulk) and their HF were comparatively incubated for 175 days at 5 and 15°C. The HF was equivalent to 70 ± 9% of the bulk CO 2 respiration as compared to a share of 63 ± 1% of bulk OC that was stored in the HF. Significant reduction of OC mineralization was found in all treatments with increasing OC content of the HF (HF-OC), clay-size minerals and Fe or Al oxyhydroxides. Temperature sensitivity (Q10) decreased with increasing soil depth from 2.4 to 1.4 in the bulk soil and from 2.9 to 1.5 in the HF. A concurrent increase in the metal-to-HF-OC ratios with soil depth suggests a stronger bonding of OM to minerals in the subsoil. There, the younger 14 C signature in CO 2 than that of the OC indicates a preferential decomposition of the more recent OM and the existence of a MOA fraction with limited access of OM to decomposers. These results indicate strong mineral controls on the decomposability of OM after permafrost thaw and on its temperature sensitivity. Thus, we here provide evidence that OM temperature sensitivity can be attenuated by MOA in permafrost soils. © 2018 John Wiley & Sons Ltd.

Impact of clay mineral on air oxidation of PAH-contaminated soils.

Science.gov (United States)

Biache, Coralie; Kouadio, Olivier; Lorgeoux, Catherine; Faure, Pierre

2014-09-01

This work investigated the impact of a clay mineral (bentonite) on the air oxidation of the solvent extractable organic matters (EOMs) and the PAHs from contaminated soils. EOMs were isolated from two coking plant soils and mixed with silica sand or bentonite. These samples, as well as raw soils and bentonite/soil mixtures, were oxidized in air at 60 and 100 °C for 160 days. Mineralization was followed by measuring the CO2 produced over the experiments. EOM, polycyclic aromatic compound (PAC), including PAH, contents were also determined. Oxidation led to a decrease in EOM contents and PAH concentrations, these diminutions were enhanced by the presence of bentonite. Transfer of carbon from EOM to insoluble organic matter pointed out a condensation phenomenon leading to a stabilization of the contamination. Higher mineralization rates, observed during the oxidation of the soil/bentonite mixtures, seem to indicate that this clay mineral had a positive influence on the transformation of PAC into CO2.

Mineralization of Nitrogen in Hydromorphic Soils Amended with ...

African Journals Online (AJOL)

... to 320.00 mg kg-1 for Mangrove soil (mangal acid sulphate soils). The order of cumulative nitrogen released in the waste amended soil followed the order: sewage sludge>kitchen waste> poultry manure> oil palm waste> cow manure. Total mineralized N indicated negative correlation with total organic N and C:N ratio ...

Occurrence and distribution of polycyclic aromatic hydrocarbons in organo-mineral particles of alluvial sandy soil profiles at a petroleum-contaminated site

International Nuclear Information System (INIS)

Lu, Zhe; Zeng, Fangang; Xue, Nandong; Li, Fasheng

2012-01-01

The occurrence and the distribution of 16 USEPA priority pollutants polycyclic aromatic hydrocarbons (PAHs) were investigated in two alluvial sandy soil profiles and in their four sizes of organo-mineral particles ( 200 μm coarse sand) beside a typical oil sludge storage site in eastern China. PAHs were mainly enriched in the surface soil (0–20 cm) and the concentrations declined in deeper soils, from 3.68 to 0.128 μg/g in profile 1 and 10.8 to 0.143 μg/g in profile 2 (dry wt.). The PAHs in the upper soil layers of this study site mainly came from combustion pollution, whereas in the lower soil layers petroleum contamination became the major source of PAHs. The content of different sized organo-mineral particles of this alluvial sandy soil decreased in the following order: fine sand > coarse sand > silt > clay. X-ray diffraction (XRD) results showed that all the different sized soil fractions of this study site were dominated by quartz, calcite and feldspar. The particle surface became smoother with size increasing as shown by scanning electron microscope (SEM) images. PAH concentrations varied largely in different sized soil fractions. The highest PAH concentration was associated with clay and decreased in the order: clay > silt > coarse sand > fine sand. Soil organic matter (SOM) content, mineral composition and particle surface characteristics were suggested as three main factors affecting the distribution of PAHs in different sized organo-mineral particles. This study will help to understand the distribution and transport characteristics of PAHs in soil profiles at petroleum-contaminated sites. -- Highlights: ► PAH concentrations varied largely in different sized fractions. ► The highest PAH concentrations were associated with clay and decreased in the order: clay > silt > coarse sand > fine sand. ► Soil organic matter (SOM) is an important factor to dominate the distribution of PAHs in this study site.

Occurrence and distribution of polycyclic aromatic hydrocarbons in organo-mineral particles of alluvial sandy soil profiles at a petroleum-contaminated site

Energy Technology Data Exchange (ETDEWEB)

Lu, Zhe [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Anwai, Dayangfang 8, Beijing 100012 (China); Department of Chemistry, University of Manitoba, Winnipeg, Manitoba, Canada R3T 2N2 (Canada); School of Environment, Renmin University of China, Zhongguancun Street 59, Beijing 100872 (China); Zeng, Fangang [School of Environment, Renmin University of China, Zhongguancun Street 59, Beijing 100872 (China); Xue, Nandong [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Anwai, Dayangfang 8, Beijing 100012 (China); Li, Fasheng, E-mail: ligulax@vip.sina.com [State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Anwai, Dayangfang 8, Beijing 100012 (China)

2012-09-01

The occurrence and the distribution of 16 USEPA priority pollutants polycyclic aromatic hydrocarbons (PAHs) were investigated in two alluvial sandy soil profiles and in their four sizes of organo-mineral particles (< 2 {mu}m clay, 2-20 {mu}m silt, 20-200 {mu}m fine sand, and > 200 {mu}m coarse sand) beside a typical oil sludge storage site in eastern China. PAHs were mainly enriched in the surface soil (0-20 cm) and the concentrations declined in deeper soils, from 3.68 to 0.128 {mu}g/g in profile 1 and 10.8 to 0.143 {mu}g/g in profile 2 (dry wt.). The PAHs in the upper soil layers of this study site mainly came from combustion pollution, whereas in the lower soil layers petroleum contamination became the major source of PAHs. The content of different sized organo-mineral particles of this alluvial sandy soil decreased in the following order: fine sand > coarse sand > silt > clay. X-ray diffraction (XRD) results showed that all the different sized soil fractions of this study site were dominated by quartz, calcite and feldspar. The particle surface became smoother with size increasing as shown by scanning electron microscope (SEM) images. PAH concentrations varied largely in different sized soil fractions. The highest PAH concentration was associated with clay and decreased in the order: clay > silt > coarse sand > fine sand. Soil organic matter (SOM) content, mineral composition and particle surface characteristics were suggested as three main factors affecting the distribution of PAHs in different sized organo-mineral particles. This study will help to understand the distribution and transport characteristics of PAHs in soil profiles at petroleum-contaminated sites. -- Highlights: Black-Right-Pointing-Pointer PAH concentrations varied largely in different sized fractions. Black-Right-Pointing-Pointer The highest PAH concentrations were associated with clay and decreased in the order: clay > silt > coarse sand > fine sand. Black-Right-Pointing-Pointer Soil organic

Record of the solar corpuscular radiation in minerals from lunar soils - A comparative study of noble gases and tracks

International Nuclear Information System (INIS)

Wieler, R.; Etique, P.

1980-01-01

A comparative study is made of trapped light noble gases and solar flare tracks in mineral separates from lunar soils in an investigation aimed at detecting possible temporal variations of the ratio between solar flare and solar wind activity. He, Ne, Ar and solar flare tracks are measured on plagioclase separates of 12 surface soils and two Apollo 15 drill core samples, and track density histograms are compared with gas concentration distributions obtained from aliquot samples. Results show that solar wind Ar is probably well retained in all minerals. He, Ne, and Ar are not saturated macroscopically, and semi-microscopic or microscopic saturation is very rare for Ar, even in gas-rich plagioclase populations. All grains contain trapped noble gases, even in relatively gas-poor mineral populations, and for clean minerals in the size range of 150-200 microns, the time between the first and last surface exposure is in the order of 10 to the 7th to 10 to the 8th years

Study of Arabian Red Sea coastal soils as potential mineral dust sources

KAUST Repository

Prakash, P. Jish; Stenchikov, Georgiy L.; Tao, Weichun; Yapici, Tahir; Warsama, Bashir H.; Engelbrecht, Johann

2016-01-01

Both Moderate Resolution Imaging Spectroradiometer (MODIS) and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) satellite observations suggest that the narrow heterogeneous Red Sea coastal region is a frequent source of airborne dust that, because of its proximity, directly affects the Red Sea and coastal urban centers. The potential of soils to be suspended as airborne mineral dust depends largely on soil texture, moisture content, and particle size distributions. Airborne dust inevitably carries the mineralogical and chemical signature of a parent soil. The existing soil databases are too coarse to resolve the small but important coastal region. The purpose of this study is to better characterize the mineralogical, chemical and physical properties of soils from the Red Sea Arabian coastal plane, which in turn will help to improve assessment of dust effect on the Red Sea and land environmental systems and urban centers. Thirteen surface soils from the hot-spot areas of wind-blown mineral dust along the Red Sea coastal plain were sampled for analysis. Analytical methods included Optical Microscopy, X-ray diffraction (XRD), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Ion Chromatography (IC), Scanning Electron Microscopy (SEM), and Laser Particle Size Analysis (LPSA). We found that the Red Sea coastal soils contain major components of quartz and feldspar, as well as lesser but variable amounts of amphibole, pyroxene, carbonate, clays, and micas, with traces of gypsum, halite, chlorite, epidote and oxides. The wide range of minerals in the soil samples was ascribed to the variety of igneous and metamorphic provenance rocks of the Arabian Shield forming the escarpment to the east of the Red Sea coastal plain. The analysis revealed that the samples contain compounds of nitrogen, phosphorus and iron that are essential nutrients to marine life. The analytical results from this study will provide a valuable input into dust emission models used

Study of Arabian Red Sea coastal soils as potential mineral dust sources

KAUST Repository

Prakash, P. Jish

2016-03-23

Both Moderate Resolution Imaging Spectroradiometer (MODIS) and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) satellite observations suggest that the narrow heterogeneous Red Sea coastal region is a frequent source of airborne dust that, because of its proximity, directly affects the Red Sea and coastal urban centers. The potential of soils to be suspended as airborne mineral dust depends largely on soil texture, moisture content, and particle size distributions. Airborne dust inevitably carries the mineralogical and chemical signature of a parent soil. The existing soil databases are too coarse to resolve the small but important coastal region. The purpose of this study is to better characterize the mineralogical, chemical and physical properties of soils from the Red Sea Arabian coastal plane, which in turn will help to improve assessment of dust effect on the Red Sea and land environmental systems and urban centers. Thirteen surface soils from the hot-spot areas of wind-blown mineral dust along the Red Sea coastal plain were sampled for analysis. Analytical methods included Optical Microscopy, X-ray diffraction (XRD), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Ion Chromatography (IC), Scanning Electron Microscopy (SEM), and Laser Particle Size Analysis (LPSA). We found that the Red Sea coastal soils contain major components of quartz and feldspar, as well as lesser but variable amounts of amphibole, pyroxene, carbonate, clays, and micas, with traces of gypsum, halite, chlorite, epidote and oxides. The wide range of minerals in the soil samples was ascribed to the variety of igneous and metamorphic provenance rocks of the Arabian Shield forming the escarpment to the east of the Red Sea coastal plain. The analysis revealed that the samples contain compounds of nitrogen, phosphorus and iron that are essential nutrients to marine life. The analytical results from this study will provide a valuable input into dust emission models used

From bulk soil to intracrystalline investigation of plant-mineral interaction

Science.gov (United States)

Lemarchand, D.; Voinot, A.; Chabaux, F.; Turpault, M.

2011-12-01

Understanding the controls and feedbacks regulating the flux of matter between bio-geochemical reservoirs in forest ecosystems receives a fast growing interest for the last decades. A complex question is to understand how minerals and vegetation interact in soils to sustain life and, to a broader scope, how forest ecosystems may respond to human activity (acid rain, harvesting,...) and climate perturbations (temperature, precipitation,...). Many mineralogical and biogeochemical approaches have longtime been developed, and occasionally coupled, in order to investigate the mechanisms by which chemical elements either are exchanged between soil particles and solutions, or are transferred to plants or to deeper soil layers and finally leave the system. But the characterization of particular processes like the contribution of minor reactive minerals to plant nutrition and global fluxes or the mechanisms by which biology can modify reaction rates and balance the bioavailability of nutrients in response to environmental perturbation sometimes fails because of the lack of suitable tracers. Recent analytical and conceptual advances have opened new perspectives for the use of light "non traditional" stable isotopes. Showing a wild range of concentrations and isotopic compositions between biogeochemical reservoirs in forest ecosystem, boron has physico-chemical properties particularly relevant to the investigation of water/rock interactions even when evolving biologically-mediated reactions. In this study, we focused on the distribution of boron isotopes from intracrystalline to bulk soil scales. An overview of the boron distribution and annual fluxes in the soil-plant system clearly indicates that the vegetation cycling largely controls the mobility of boron. We also observe that the mineral and biological B pools have drastically different isotopic signature that makes the transfer of B between them very easy to follow. In particular, the podzol soil we analyzed shows a

Net sulfur mineralization potential in Swedish arable soils in relation to long-term treatment history and soil properties

DEFF Research Database (Denmark)

Boye, Kristin; Nilsson, S Ingvar; Eriksen, Jørgen

2009-01-01

accumulated net S mineralization (SAccMin) and a number of soil physical and chemical properties were determined. Treatments and soil differences in SAccMin, as well as correlations with soil variables, were tested with single and multivariate analyses. Long-term FYM application resulted in a significantly (p......The long-term treatment effect (since 1957-1966) of farmyard manure (FYM) application compared with crop residue incorporation was investigated in five soils (sandy loam to silty clay) with regards to the net sulfur (S) mineralization potential. An open incubation technique was used to determine...... = 0.012) higher net S mineralization potential, although total amounts of C, N, and S were not significantly (p soils within this treatment. The measured soil variables were not significantly correlated...

A Combination of Biochar-Mineral Complexes and Compost Improves Soil Bacterial Processes, Soil Quality, and Plant Properties.

Science.gov (United States)

Ye, Jun; Zhang, Rui; Nielsen, Shaun; Joseph, Stephen D; Huang, Danfeng; Thomas, Torsten

2016-01-01

Organic farming avoids the use of synthetic fertilizers and promises food production with minimal environmental impact, however this farming practice does not often result in the same productivity as conventional farming. In recent years, biochar has received increasing attention as an agricultural amendment and by coating it with minerals to form biochar-mineral complex (BMC) carbon retention and nutrient availability can be improved. However, little is known about the potential of BMC in improving organic farming. We therefore investigated here how soil, bacterial and plant properties respond to a combined treatment of BMC and an organic fertilizer, i.e., a compost based on poultry manure. In a pakchoi pot trial, BMC and compost showed synergistic effects on soil properties, and specifically by increasing nitrate content. Soil nitrate has been previously observed to increase leaf size and we correspondingly saw an increase in the surface area of pakchoi leaves under the combined treatment of BMC and composted chicken manure. The increase in soil nitrate was also correlated with an enrichment of bacterial nitrifiers due to BMC. Additionally, we observed that the bacteria present in the compost treatment had a high turnover, which likely facilitated organic matter degradation and a reduction of potential pathogens derived from the manure. Overall our results demonstrate that a combination of BMC and compost can stimulate microbial process in organic farming that result in better vegetable production and improved soil properties for sustainable farming.

A combination of biochar-mineral complexes and compost improves soil bacterial processes, soil quality and plant properties

Directory of Open Access Journals (Sweden)

JUN eYE

2016-04-01

Full Text Available Organic farming avoids the use of synthetic fertilizers and promises food production with minimal environmental impact, however this farming practice does not often result in the same productivity as conventional farming. In recent years, biochar has received increasing attention as an agricultural amendment and by coating it with minerals to form biochar-mineral complex (BMC carbon retention and nutrient availability can be improved. However, little is known about the potential of BMC in improving organic farming. We therefore investigated here how soil, bacterial and plant properties respond to a combined treatment of BMC and an organic fertilizer, i.e. a compost based on poultry manure. In a pakchoi pot trial, BMC and compost showed synergistic effects on soil properties, and specifically by increasing nitrate content. Soil nitrate has been previously observed to increase leaf size and we correspondingly saw an increase in the surface area of pakchoi leaves under the combined treatment of BMC and chicken manure. The increase in soil nitrate was also correlated with an enrichment of bacterial nitrifiers due to BMC. Additionally, we observed that the bacteria present in the compost treatment had a high turnover, which likely facilitated organic matter degradation and a reduction of potential pathogens derived from the manure. Overall our results demonstrate that a combination of BMC and compost can stimulate microbial process in organic farming that result in better vegetable production and improved soil properties for sustainable farming.

Ex situ bioremediation of mineral oil in soils: Aerated pile treatment. Final report

International Nuclear Information System (INIS)

Graves, D.

1998-04-01

Under a contract with Southern Company Services, a pilot-scale evaluation of mineral oil biodegradation was conducted at Plant Mitchell. The evaluation consisted of two demonstrations to examine land treatment and aerated pile treatment of soil contaminated with the mineral insulating oil used in electrical transformers. Treatment of mineral oil contaminated soil is problematic in the State of Georgia and throughout the US because current practice is to excavate and landfill the contaminated soil. In many cases, the cost associated with these activities far exceeds the environmental risk of mineral oil in soil. This project was designed to evaluate the performance of bioremediation for the treatment of mineral oil in soil. Testing was carried out in a demonstration facility prepared by Georgia Power Company. The facility consisted of 12 independent treatment cells constructed on a concrete pad and covered with a roof

[Effects of variable temperature on organic carbon mineralization in typical limestone soils].

Science.gov (United States)

Wang, Lian-Ge; Gao, Yan-Hong; Ding, Chang-Huan; Ci, En; Xie, De-Ti

2014-11-01

Soil sampling in the field and incubation experiment in the laboratory were conducted to investigate the responses of soil organic carbon (SOC) mineralization to variable temperature regimes in the topsoil of limestone soils from forest land and dry land. Two incubated limestone soils were sampled from the 0-10 cm layers of typical forest land and dry land respectively, which were distributed in Tianlong Mountain area of Puding county, Guizhou province. The soils were incubated for 56 d under two different temperature regimes including variable temperature (range: 15-25 degrees C, interval: 12 h) and constant temperature (20 degrees C), and the cumulative temperature was the same in the two temperature treatments. In the entire incubation period (56 d), the SOC cumulative mineralization (63.32 mg x kg(-1)) in the limestone soil from dry land (SH) under the variable temperature was lower than that (63.96 mg x kg(-1)) at constant 20 degrees C, and there was no significant difference in the SOC cumulative mineralization between the variable and constant temperature treatments (P variable temperature was significantly lower than that (209.52 mg x kg(-1)) at constant 20 degrees C. The results indicated that the responses of SOC mineralization to the variable temperature were obviously different between SL and SH soils. The SOC content and composition were significantly different between SL and SH soils affected by vegetation and land use type, which suggested that SOC content and composition were important factors causing the different responses of SOC mineralization to variable temperature between SL and SH soils. In addition, the dissolved organic carbon (DOC) content of two limestone soils were highly (P variable temperature mainly influenced SOC mineralization by changing microbial community activity rather than by changing microbial quantity.

Differential chemical fractionation of dissolved organic matter during sorption by Fe mineral phases in a tropical soil from the Luquillo Critical Zone Observatory

Science.gov (United States)

Plante, A. F.; Coward, E.; Ohno, T.; Thompson, A.

2017-12-01

Fe-bearing mineral phases contribute substantially to adsorption and stabilization of soil organic matter (SOM), due largely to their high specific surface area (SSA) and reactivity. While the importance of adsorption onto mineral surfaces has been well-elucidated, selectivity of various mineral and organic phases remains poorly understood. The goals of this work were to: 1) quantify the contributions of Fe-minerals of varying crystallinity to dissolved organic matter (DOM) sorption, and 2) characterize the molecular fractionation of DOM induced by reactions at the mineral interface, using a highly-weathered Oxisol from the Luquillo Critical Zone Observatory (LCZO). Three selective dissolution experiments targeting Fe-mineral phases were followed by specific surface area (SSA) analysis of the residues and characterization of extracted DOM by high resolution mass spectrometry (FT-ICR-MS). Fe-depleted extraction residue samples, untreated control soil samples, and Fe-enriched ferrihydrite-coated soil samples were then subjected to a batch sorption experiment with litter-derived DOM. Results of selective dissolution experiments indicated that a substantial proportion of soil SSA was derived from extracted Fe-bearing phases, and FT-ICR-MS analysis of extracted DOM revealed distinct chemical signatures. Sorbed C concentrations were well correlated with Fe contents induced by treatments, and thus SSA. Molecular characterization of the DOM post-sorption indicated that poorly crystalline Fe phases preferentially adsorbed highly unsaturated aromatic compounds, and higher-crystallinity Fe phases were associated with more aliphatic compounds. These findings suggests that molecular fractionation via organomineral complexation may act as a physicochemical filter of DOM released to the critical zone.

Soil carbon mineralization following biochar addition associated with external nitrogen

Directory of Open Access Journals (Sweden)

Rudong Zhao

2015-12-01

Full Text Available Biochar has been attracting increasing attention for its potentials of C sequestration and soil amendment. This study aimed to understand the effects of combining biochar with additional external N on soil C mineralization. A typical red soil (Plinthudults was treated with two biochars made from two types of plantation-tree trunks (soil-biochar treatments, and was also treated with external N (soil-biochar-N treatments. All treatments were incubated for 42 d. The CO2-C released from the treatments was detected periodically. After the incubation, soil properties such as pH, microbial biomass C (MBC, and microbial biomass N (MBN were measured. The addition of biochar with external N increased the soil pH (4.31-4.33 compared to the soil treated with external N only (4.21. This was not observed in the comparison of soil-biochar treatments (4.75-4.80 to soil only (4.74. Biochar additions (whether or not they were associated with external N increased soil MBC and MBN, but decreased CO2-C value per unit total C (added biochar C + soil C according to the model fitting. The total CO2-C released in soil-biochar treatments were enhanced compared to soil only (i.e., 3.15 vs. 2.57 mg and 3.23 vs. 2.45 mg, which was attributed to the labile C fractions in the biochars and through soil microorganism enhancement. However, there were few changes in soil C mineralization in soil-biochar-N treatments. Additionally, the potentially available C per unit total C in soil-biochar-N treatments was lower than that observed in the soil-biochar treatments. Therefore, we believe in the short term, that C mineralization in the soil can be enhanced by biochar addition, but not by adding external N concomitantly.

Effect of N and P addition on soil organic C potential mineralization in forest soils in South China

Institute of Scientific and Technical Information of China (English)

OUYANG Xuejun; ZHOU Guoyi; HUANG Zhongliang; ZHOU Cunyu; LI Jiong; SHI Junhui; ZHANG Deqiang

2008-01-01

Atmospheric nitrogen deposition is at a high level in some forests of South China. The effects of addition of exogenous N and P on soil organic carbon mineralization were studied to address: (1) if the atmospheric N deposition promotes soil C storage through decreasing mineralization; (2) if the soil available P is a limitation to organic carbon mineralization. Soils (0-10 cm) was sampled from monsoon evergreen broad-leaved forest (MEBF), coniferous and broad-leaved mixed forest (CBMF), and Pinus massoniana forest (PMF) in Dinghushan Biosphere Reserve (located in Gnangdong Province, China). The soils were incubated at 25℃ for 45 weeks, with addition of N (NH4NO3 solution) or P (KH2PO4 solution). CO2-C emission and the inorganic N (NH4+-N and NO3--N) of the soils were determined during the incubation. The results showed that CO2-C emission decreased with the N addition. The addition of P led to a short-term sharp increase in CO2 emission after P application, and the responses of CO2-C evolution to P addition in the later period of incubation related to forest types. Strong P inhibition to CO2 emission occurred in both PMF and CBMF soils in the later incubation. The two-pool kinetic model was fitted well to the data for C turnover in this experiment. The model analysis demonstrated that the addition of N and P changed the distribution of soil organic C between the labile and recalcitrant pool, as well as their mineralization rates. In our experiment, soil pH can not completely explain the negative effect of N addition on CO2-C emission. The changes of soil inorganic N during incubation seemed to support the hypothesis that the polymerization of added nitrogen with soil organic compound by abiotic reactions during incubation made the added nitrogen retard the soil organic carbon mineralization. We conclude that atmospheric N deposition contributes to soil C accretion in the three subtropical forest ecosystems, however, the shortage of soil available P in CBMF and

[Soil organic carbon mineralization of Black Locust forest in the deep soil layer of the hilly region of the Loess Plateau, China].

Science.gov (United States)

Ma, Xin-Xin; Xu, Ming-Xiang; Yang, Kai

2012-11-01

The deep soil layer (below 100 cm) stores considerable soil organic carbon (SOC). We can reveal its stability and provide the basis for certification of the deep soil carbon sinks by studying the SOC mineralization in the deep soil layer. With the shallow soil layer (0-100 cm) as control, the SOC mineralization under the condition (temperature 15 degrees C, the soil water content 8%) of Black Locust forest in the deep soil layer (100-400 cm) of the hilly region of the Loess Plateau was studied. The results showed that: (1) There was a downward trend in the total SOC mineralization with the increase of soil depth. The total SOC mineralization in the sub-deep soil (100-200 cm) and deep soil (200-400 cm) were equivalent to approximately 88.1% and 67.8% of that in the shallow layer (0-100 cm). (2) Throughout the carbon mineralization process, the same as the shallow soil, the sub-deep and deep soil can be divided into 3 stages. In the rapid decomposition phase, the ratio of the mineralization or organic carbon to the total mineralization in the sub-deep and deep layer (0-10 d) was approximately 50% of that in the shallow layer (0-17 d). In the slow decomposition phase, the ratio of organic carbon mineralization to total mineralization in the sub-deep, deep layer (11-45 d) was 150% of that in the shallow layer (18-45 d). There was no significant difference in this ratio among these three layers (46-62 d) in the relatively stable stage. (3) There was no significant difference (P > 0.05) in the mineralization rate of SOC among the shallow, sub-deep, deep layers. The stability of SOC in the deep soil layer (100-400 cm) was similar to that in the shallow soil layer and the SOC in the deep soil layer was also involved in the global carbon cycle. The change of SOC in the deep soil layer should be taken into account when estimating the effects of soil carbon sequestration in the Hilly Region of the Loess Plateau, China.

[Effects of different types of litters on soil organic carbon mineralization].

Science.gov (United States)

Shi, Xue-Jun; Pan, Jian-Jun; Chen, Jin-Ying; Yang, Zhi-Qiang; Zhang, Li-Ming; Sun, Bo; Li, Zhong-Pei

2009-06-15

Using litter incubation experiment in laboratory, decomposition discrepancies of four typical litters from Zijin Mountain were analyzed. The results show that organic carbon mineralization rates of soil with litters all involve fast and slow decomposition stages, and the differences are that the former has shorter duration,more daily decomposition quantity while the latter is opposite. Organic carbon mineralization rates of soil with litters rapidly reached maximum in the early days of incubation, and the order is soil with Cynodon dactylon litter (CK + BMD) (23.88 +/- 0.62) mg x d(-1), soil with Pinus massoniana litter (CK+ PML) (17.93 +/- 0.99) mg x d(-1), soil with Quercus acutissima litter (CK+ QAC) (15.39 +/- 0.16) mg x d(-1) and soil with Cyclobalanopsis glauca litter (CK + CGO) (7.26 +/- 0.34) mg x d(-1), and with significant difference between each other (p litter initial chemical elements. The amount of organic carbon mineralized accumulation within three months incubation is (CK + BMD) (338.21 +/- 6.99) mg, (CK + QAC) (323.48 +/- 13.68) mg, (CK + PML) (278.34 +/- 13.91) mg and (CK + CGO) (245.21 +/- 4.58) mg. 198.17-297.18 mg CO2-C are released during litter incubation, which occupies 20.29%-31.70% of the total litter organic carbon amounts. Power curve model can describe the trends of organic carbon mineralization rate and mineralized accumulation amount,which has a good correlation with their change.

Surface analytical techniques applied to minerals processing

International Nuclear Information System (INIS)

Smart, R.St.C.

1991-01-01

An understanding of the chemical and physical forms of the chemically altered layers on the surfaces of base metal sulphides, particularly in the form of hydroxides, oxyhydroxides and oxides, and the changes that occur in them during minerals processing lies at the core of a complete description of flotation chemistry. This paper reviews the application of a variety of surface-sensitive techniques and methodologies applied to the study of surface layers on single minerals, mixed minerals, synthetic ores and real ores. Evidence from combined XPS/SAM/SEM studies have provided images and analyses of three forms of oxide, oxyhydroxide and hydroxide products on the surfaces of single sulphide minerals, mineral mixtures and complex sulphide ores. 4 refs., 2 tabs., 4 figs

Particulate Organic Matter Affects Soil Nitrogen Mineralization under Two Crop Rotation Systems.

Directory of Open Access Journals (Sweden)

Rongyan Bu

Full Text Available Changes in the quantity and/or quality of soil labile organic matter between and after different types of cultivation system could play a dominant role in soil nitrogen (N mineralization. The quantity and quality of particulate organic matter (POM and potentially mineralizable-N (PMN contents were measured in soils from 16 paired rice-rapeseed (RR/cotton-rapeseed (CR rotations sites in Hubei province, central China. Then four paired soils encompassing low (10th percentile, intermediate (25th and 75th percentiles, and high (90th percentile levels of soil PMN were selected to further study the effects of POM on soil N mineralization by quantifying the net N mineralization in original soils and soils from which POM was removed. Both soil POM carbon (POM-C and N (POM-N contents were 45.8% and 55.8% higher under the RR rotation compared to the CR rotation, respectively. The PMN contents were highly correlated with the POM contents. The PMN and microbial biomass N (MBN contents concurrently and significantly decreased when POM was removed. The reduction rate of PMN was positively correlated with changes in MBN after the removal of POM. The reduction rates of PMN and MBN after POM removal are lower under RR rotations (38.0% and 16.3%, respectively than CR rotations (45.6% and 19.5%, respectively. Furthermore, infrared spectroscopy indicated that compounds with low-bioavailability accumulated (e.g., aromatic recalcitrant materials in the soil POM fraction under the RR rotation but not under the CR rotation. The results of the present study demonstrated that POM plays a vital role in soil N mineralization under different rotation systems. The discrepancy between POM content and composition resulting from different crop rotation systems caused differences in N mineralization in soils.

Effect of heavy metals on soil mineral surfaces and bioretention pond performance

Science.gov (United States)

Zhang, H.; Olson, M. S.

2009-12-01

Haibo Zhang and Mira S. Olson Department of Civil, Architectural, and Environmental Engineering, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104 As urban stormwater runoff flows across impervious surfaces, it collects and accumulates pollutants that are detrimental to the quality of local receiving water bodies. Heavy metal pollution, such as copper, lead and zinc, has been a concern in urban stormwater runoff. In addition, the presence of bacteria in stormwater has been frequently reported. The co-existence of both heavy metals and bacteria in stormwater and their complex interactions determine their transport and removal through bioretention pond. Stormwater runoff was sampled from a bioretention pond in Philadelphia, PA. The concentration of copper, lead and zinc were measured as 0.086ppm, 0.083ppm and 0.365ppm, respectively. Batch experiments were conducted with solutions of pure copper, lead and zinc, and with a synthetic stormwater solution amended with copper, lead and zinc. The solution was buffered to pH 7, within the range of the observed stormwater pH. In pure heavy metal solutions, the sorption of copper, lead and zinc onto soil are 96%, 99% and 85%, respectively. In synthetic stormwater containing nutrients and all three metals, the sorption of lead is 97%, while copper and zinc decrease to 29% and 71%, respectively. Mineralogy of a soil sample taken from the bioretention pond was analyzed using a scanning electron microscope (SEM) and compared before and after sorption experiments. Sorption and complexation of heavy metals is likely to change the mineralogy of soil particle surfaces, which will affect the attachment of bacteria and therefore its transport through soil. This study will benefit long-term predictions of the performance of bioretention ponds for urban stormwater runoff treatment. Keyword: Heavy metal pollution, sorption, surface complexation, urban stormwater runoff, bioretention pond

Mineralization of nitrogen by protozoan activity in soil

NARCIS (Netherlands)

Kuikman, P.

1990-01-01

In general, more than 95% of the nitrogen in soils is present in organic forms. This nitrogen is not directly available to plants unless microbial decomposition takes place with the release of mineral nitrogen. In modern agriculture, nitrogen is often applied to arable soils as a fertilizer

Organic matter dynamics and N mineralization in grassland soils

OpenAIRE

Hassink, J.

1995-01-01

The aims of this study are i) to improve our understanding of the interactions between soil texturelsoil structure, soil organic matter, soil biota and mineralization in grassland soils, ii) to develop a procedure that yields soil organic matter fractions that can be determined directly and can be used in soil organic matter models, iii) to develop a model that predicts the long-term dynamics of soil organic matter, iv) to develop a simple model that can be used by farmers and advi...

Stabilization of organic matter in soils: role of amorphous mineral phases

Science.gov (United States)

Zewde Tamrat, Wuhib; Rose, Jérôme; Levard, Clément; Chaurand, Perrine; Basile-Doelsch, Isabelle

2016-04-01

Soil organic matter (SOM) globally contributes the largest portion of continental carbon stock. One major issue concerning this large C pool includes its instability by mineralization and erosion due to land use. The main hypothesis of this work is that physicochemical stabilization of SOM is mainly driven by interactions of organic compounds, not with mineral surfaces as classically considered, but with amorphous polymers continuously formed by the alteration of soil minerals(1-3). Our objective is to understand how nano-organomineral complexes (nCOMx) are structured at the nanoscale, assess mechanisms of their formation, and quantify the effects of their occurrence on SOM turnovers. Due to inherent high complexity of natural samples, our methodology is based on the formation of nCOMx from both synthetic systems and natural mineral-weathered components. For the mineral component, biotite (from Bancroft, Canada) was selected. For the organic component, 3,4-Dihydroxy-L-phenylalanine, an amino acid with hydroxyl (pKa=9.95), carboxyl (pKa=2,58), amino (pKa=9,24) and an aromatic functions was chosen. The methodology aimed at developing conditions that generate biotite dissolution and nCOMx precipitation. The second step of the experiment consisted of the precipitation of nCOMx by slowly increasing pH over 3 to 12 hours of hydrolysis. Three final pH conditions were tested (4.2, 5 and 7) with Metal/Carbon ratios of 0.01, 0.1, 1, 10 and 'No Carbon'. The first results of dissolution rates and congruency, AFM imaging, ICPMS, HR-TEM and XRD as well as XAS characterizations (transmission and florescence mode at the Fe K-edge) of nCOMx will be presented. Experiments and analysis techniques were designed to study these synthetic phases with regard to Si, Al, Fe and OM proportions to increase the OM proportion (as in natural soil phases) and also increase the stability of the OM phase (as in increased residence time of OM in the soil). We will focus particularly on the Fe state

Leaf litter and roots as sources of mineral soil organic matter in temperate deciduous forest with and without earthworms

Science.gov (United States)

Fahey, T.; Yavitt, J. B.

2012-12-01

We labeled sugar maple trees with 13C to quantify the separate contributions of decaying leaf litter and root turnover/rhizosphere C flux to mineral soil organic matter (SOM). Labeled leaf litter was applied to forest plots with and without earthworms and recovery of the label in SOM was quantified over three years. In parallel, label recovery was quantified in soils from the labeling chambers where all label was supplied by belowground C flux. In the absence of earthworms about half of the label added as leaf litter remained in the surface organic horizons after three years, with about 3% recovered in mineral SOM. The label was most enriched on silt + clay surfaces, representing precipitation of DOC derived from litter. Earthworms mixed nearly all the leaf litter into mineral soil within one year, and after two years the label was most enriched in particulate organic matter held within soil aggregates produced by worms. After three years 15-20% of the added label was recovered in mineral SOM. In the labeling chambers over 75% of belowground C allocation (BCA) was used in root and rhizosphere respiration in the first year after labeling. We recovered only 3.8% of estimated BCA in SOM after 3 years; however, expressed as a proportion of fine root production plus rhizosphere C flux, this value is 15.4%, comparable to that for leaf litter in the presence of earthworms. In conclusion, both roots and leaf litter contribute significantly to the formation of stabilized mineral SOM in temperate deciduous forests, and this process is profoundly altered by the invasion of lumbricid earthworms.

Metal oxides, clay minerals and charcoal determine the composition of microbial communities in matured artificial soils and their response to phenanthrene.

Science.gov (United States)

Babin, Doreen; Ding, Guo-Chun; Pronk, Geertje Johanna; Heister, Katja; Kögel-Knabner, Ingrid; Smalla, Kornelia

2013-10-01

Microbial communities in soil reside in a highly heterogeneous habitat where diverse mineral surfaces, complex organic matter and microorganisms interact with each other. This study aimed to elucidate the long-term effect of the soil mineral composition and charcoal on the microbial community composition established in matured artificial soils and their response to phenanthrene. One year after adding sterile manure to different artificial soils and inoculating microorganisms from a Cambisol, the matured soils were spiked with phenanthrene or not and incubated for another 70 days. 16S rRNA gene and internal transcribed spacer fragments amplified from total community DNA were analyzed by denaturing gradient gel electrophoresis. Metal oxides and clay minerals and to a lesser extent charcoal influenced the microbial community composition. Changes in the bacterial community composition in response to phenanthrene differed depending on the mineral composition and presence of charcoal, while no shifts in the fungal community composition were observed. The abundance of ring-hydroxylating dioxygenase genes was increased in phenanthrene-spiked soils except for charcoal-containing soils. Here we show that the formation of biogeochemical interfaces in soil is an ongoing process and that different properties present in artificial soils influenced the bacterial response to the phenanthrene spike. © 2012 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.

Interactive priming of biochar and labile organic matter mineralization in a smectite-rich soil.

Science.gov (United States)

Keith, Alexandra; Singh, Balwant; Singh, Bhupinder Pal

2011-11-15

Biochar is considered as an attractive tool for long-term carbon (C) storage in soil. However, there is limited knowledge about the effect of labile organic matter (LOM) on biochar-C mineralization in soil or the vice versa. An incubation experiment (20 °C) was conducted for 120 days to quantify the interactive priming effects of biochar-C and LOM-C mineralization in a smectitic clayey soil. Sugar cane residue (source of LOM) at a rate of 0, 1, 2, and 4% (w/w) in combination with two wood biochars (450 and 550 °C) at a rate of 2% (w/w) were applied to the soil. The use of biochars (~ -36‰) and LOM (-12.7‰) or soil (-14.3‰) with isotopically distinct δ(13)C values allowed the quantification of C mineralized from biochar and LOM/soil. A small fraction (0.4-1.1%) of the applied biochar-C was mineralized, and the mineralization of biochar-C increased significantly with increasing application rates of LOM, especially during the early stages of incubation. Concurrently, biochar application reduced the mineralization of LOM-C, and the magnitude of this effect increased with increasing rate of LOM addition. Over time, the interactive priming of biochar-C and LOM-C mineralization was stabilized. Biochar application possesses a considerable merit for long-term soil C-sequestration, and it has a stabilizing effect on LOM in soil.

Effects of Sludge-amendment on Mineralization of Pyrene and Microorganisms in Sludge and Soil

DEFF Research Database (Denmark)

Klinge, C; Gejlsbjerg, B; Ekelund, Flemming

2001-01-01

. Sludge-amendment enhanced the mineralization of pyrene in the soil compared to soil without sludge, and the most extensive mineralization was observed when the sludge was kept in a lump. The number of protozoa, heterotrophic bacteria and pyrene-mineralizing bacteria was much higher in the sludge compared...... to the soil. The amendment of sludge did not affect the number of protozoa and bacteria in the surrounding soil, which indicated that organic contaminants in the sludge had a little effect on the number of protozoa and bacteria in the surrounding soil...

How do peat type, sand addition and soil moisture influence the soil organic matter mineralization in anthropogenically disturbed organic soils?

Science.gov (United States)

Säurich, Annelie; Tiemeyer, Bärbel; Don, Axel; Burkart, Stefan

2017-04-01

Drained peatlands are hotspots of carbon dioxide (CO2) emissions from agriculture. As a consequence of both drainage induced mineralization and anthropogenic sand mixing, large areas of former peatlands under agricultural use contain soil organic carbon (SOC) at the boundary between mineral and organic soils. Studies on SOC dynamics of such "low carbon organic soils" are rare as the focus of previous studies was mainly either on mineral soils or "true" peat soil. However, the variability of CO2 emissions increases with disturbance and therefore, we have yet to understand the reasons behind the relatively high CO2 emissions of these soils. Peat properties, soil organic matter (SOM) quality and water content are obviously influencing the rate of CO2 emissions, but a systematic evaluation of the hydrological and biogeochemical drivers for mineralization of disturbed peatlands is missing. With this incubation experiment, we aim at assessing the drivers of the high variability of CO2 emissions from strongly anthropogenically disturbed organic soil by systematically comparing strongly degraded peat with and without addition of sand under different moisture conditions and for different peat types. The selection of samples was based on results of a previous incubation study, using disturbed samples from the German Agricultural Soil Inventory. We sampled undisturbed soil columns from topsoil and subsoil (three replicates of each) of ten peatland sites all used as grassland. Peat types comprise six fens (sedge, Phragmites and wood peat) and four bogs (Sphagnum peat). All sites have an intact peat horizon that is permanently below groundwater level and a strongly disturbed topsoil horizon. Three of the fen and two of the bog sites have a topsoil horizon altered by sand-mixing. In addition the soil profile was mapped and samples for the determination of soil hydraulic properties were collected. All 64 soil columns (including four additional reference samples) will be installed

Determination of soil weathering rates with U-Th series disequilibria: approach on bulk soil and selected mineral phases

International Nuclear Information System (INIS)

Gontier, Adrien

2014-01-01

The aim of the present study was to evaluate weathering and soil formation rates using U-Th disequilibria in bulk soil or separated minerals. The specific objectives of this work were to evaluate the use of U-Th chronometric tools 1) regarding the impact of a land cover change and the bedrock characteristics 2) in selected secondary mineral phases and 3) in primary minerals. On the Breuil-Chenue (Morvan) site, no vegetation effect neither a grain size effect was observed on the U-Th series in the deepest soil layers (≤ 40 cm). The low soil production rate (1-2 mm/ka) is therefore more affected by regional geomorphology than by the underlying bedrock texture. In the second part of this work, based on a thorough evaluation of different techniques, a procedure was retained to extract Fe-oxides without chemical fractionation. Finally, the analysis of biotites hand-picked from one of the studied soil profile showed that U-series disequilibria allow to independently determinate the field-weathering-rate of minerals. (author)

Phosphate-Solubilizing and -Mineralizing Abilities of Bacteria Isolated from Soils

Institute of Scientific and Technical Information of China (English)

TAO Guang-Can; TIAN Shu-Jun; CAI Miao-Ying; XIE Guang-Hui

2008-01-01

Microorganisms capable of solubilizing and mineralizing phosphorus (P) pools in soils are considered vital in promoting P bioavailability. The study was conducted to screen and isolate inorganic P-solubilizing bacteria (IPSB) and organic P-mineralizing bacteria (OPMB) in soils taken from subtropical flooded and temperate non-flooded soils, and to compare inorganic P-solubilizing and organic P-solubilizing abilities between IPSB and OPMB. Ten OPMB strains were isolated and identified as Bacillus cereus and Bacillus megaterium, and five IPSB strains as B. megaterium, Burkholderia caryophylli,Pseudomonas ciehorii, and Pseudomonas syringae. P-solubilizing and -mineralizing abilities of the strains were measured using the methods taking cellular P into account. The IPSB strains exhibited inorganic P-sohibilizing abilities ranging between 25.4-41.7 μg P mL-1 and organic P-mineralizing abilities between 8.2-17.8 μg P mL-1. Each of the OPMB strains also exhibited both solubilizing and mineralizing abilities varying from 4.4 to 26.5 μg P mL-1 and from 13.8 to 62.8 μg P mL-1, respectively. For both IPSB and OPMB strains, most of the P mineralized from the organic P source was incorporated into the bacterial cells as cellular P. A significantly negative linear correlation (P < 0.05) was found between culture pH and P solubilized from inorganic P by OPMB strains. The results suggested that P solubilization and mineralization could coexist in the same bacterial strain.

Carbon content of forest floor and mineral soil in Mediterranean Pinus spp. and Oak stands in acid soils in Northern Spain

Energy Technology Data Exchange (ETDEWEB)

Herrero, C.; Turrión, M.B.; Pando, V.; Bravo, F.

2016-07-01

Aim of the study: The aim of the study was to determine the baseline carbon stock in forest floor and mineral soils in pine and oak stands in acid soils in Northern Spain. Area of study: The study area is situated in northern Spain (42° N, 4° W) on “Paramos y Valles” region of Palencia. aterial and methods: An extensive monitoring composed of 48 plots (31 in pine and 17 in oak stands) was carried out. Litter layers and mineral soil samples, at depths of 0-30 cm and 30-60 cm, were taken in each plot. An intensive monitoring was also performed by sampling 12 of these 48 plots selected taken in account species forest composition and their stand development stage. Microbial biomass C (CMB), C mineralization (CRB), and soil organic C balance at stand level were determined in surface soil samples of intensive monitoring. Main results: No differences in soil C content were detected in the two forest ecosystems up to 60 cm depth (53.0±25.8 Mg C ha-1 in Pinus spp. plantations and 60.3±43.8 Mg C ha-1 in oak stands). However, differences in total C (CT), CMB and CRB were found in the upper 10 cm of the soils depending on the stand development stage in each species forest composition (Pinus nigra, Pinus pinaster, Pinus sylvestris and Quercus pyrenaica). Plots with high development stage exhibited significant lower metabolic quotient (qCO2), so, meant more efficient utilization of C by the microbial community. The C content in the forest floor was higher in pine stands (13.7±0.9 Mg C ha-1) than in oak stands (5.4±0.7 Mg C ha-1). A greater turnover time was found in pine ecosystems vs. oak stands. In contrast, forest floor H layer was nonexistent in oak stands. Research highlights: Results about litterfall, forest floor and mineral soil dynamics in this paper can be used strategically to reach environmental goals in new afforestation programs and sustainable forest management approaches. (Author)

Biologically enhanced mineral weathering: what does it look like, can we model it?

Science.gov (United States)

Schulz, M. S.; Lawrence, C. R.; Harden, J. W.; White, A. F.

2011-12-01

The interaction between plants and minerals in soils is hugely important and poorly understood as it relates to the fate of soil carbon. Plant roots, fungi and bacteria inhabit the mineral soil and work symbiotically to extract nutrients, generally through low molecular weight exudates (organic acids, extracelluar polysachrides (EPS), siderophores, etc.). Up to 60% of photosynthetic carbon is allocated below ground as roots and exudates, both being important carbon sources in soils. Some exudates accelerate mineral weathering. To test whether plant exudates are incorporated into poorly crystalline secondary mineral phases during precipitation, we are investigating the biologic-mineral interface. We sampled 5 marine terraces along a soil chronosequence (60 to 225 ka), near Santa Cruz, CA. The effects of the biologic interactions with mineral surfaces were characterized through the use of Scanning Electron Microscopy (SEM). Morphologically, mycorrhizal fungi were observed fully surrounding minerals, fungal hyphae were shown to tunnel into primary silicate minerals and we have observed direct hyphal attachment to mineral surfaces. Fungal tunneling was seen in all 5 soils by SEM. Additionally, specific surface area (using a nitrogen BET method) of primary minerals was measured to determine if the effects of mineral tunneling are quantifiable in older soils. Results suggest that fungal tunneling is more extensive in the primary minerals of older soils. We have also examined the influence of organic acids on primary mineral weathering during soil development using a geochemical reactive transport model (CrunchFlow). Addition of organic acids in our models of soil development at Santa Cruz result in decreased activity of Fe and Al in soil pore water, which subsequently alters the spatial extent of primary mineral weathering and kaolinite precipitation. Overall, our preliminary modeling results suggest biological processes may be an important but underrepresented aspect of

Microfluidic Leaching of Soil Minerals: Release of K+ from K Feldspar

Science.gov (United States)

Ciceri, Davide; Allanore, Antoine

2015-01-01

The rate of K+ leaching from soil minerals such as K-feldspar is believed to be too slow to provide agronomic benefit. Currently, theories and methods available to interpret kinetics of mineral processes in soil fail to consider its microfluidic nature. In this study, we measure the leaching rate of K+ ions from a K-feldspar-bearing rock (syenite) in a microfluidic environment, and demonstrate that at the spatial and temporal scales experienced by crop roots, K+ is available at a faster rate than that measured with conventional apparatuses. We present a device to investigate kinetics of mineral leaching at an unprecedented simultaneous resolution of space (~101-102 μm), time (~101-102 min) and fluid volume (~100-101 mL). Results obtained from such a device challenge the notion that silicate minerals cannot be used as alternative fertilizers for tropical soils. PMID:26485160

Mineralization and volatilization of ring labelled 14C-2,4-D in three different soils

International Nuclear Information System (INIS)

Shrivastwa, M.; Singh, D.K.; Jindal, T.; Agarwal, H.C.

2001-01-01

Mineralization and volatilization of ring labelled 14 C-2,4-dichlorophenoxyacetic acid in soil was studied over a period of six weeks under laboratory conditions at 25 deg. C in three different soils collected from three sites, Delhi, Jaipur and Ludhiana. A very slow rate of both mineralization and volatilization was observed in all the three soils. The observed mineralization, was highest for the Delhi soil, 0.93%, followed by the Ludhiana soil, 0.73% and the Jaipur soil 0.14% in 42 days. The extent of volatilization was 0.46% for the Jaipur soil, 0.37% for the Ludhiana soil and 0.32% for the Delhi soil. (author)

Soil Organic Matter and Soil Productivity: Searching for the Missing Link

Science.gov (United States)

Felipe G. Sanchez

1998-01-01

Soil-organic matter (SOM) is a complex array of components including soil fauna and flora at different stages of decomposition (Berg et al., 1982). Its concentration in soils can vary from 0.5% in mineral soils to almost 100% in peat soils (Brady, 1974). Organic matter (OM) in the surface mineral soil is considered a major determinant of forest ecosystem productivity...

Hyperspectral analysis of clay minerals

Science.gov (United States)

Janaki Rama Suresh, G.; Sreenivas, K.; Sivasamy, R.

2014-11-01

A study was carried out by collecting soil samples from parts of Gwalior and Shivpuri district, Madhya Pradesh in order to assess the dominant clay mineral of these soils using hyperspectral data, as 0.4 to 2.5 μm spectral range provides abundant and unique information about many important earth-surface minerals. Understanding the spectral response along with the soil chemical properties can provide important clues for retrieval of mineralogical soil properties. The soil samples were collected based on stratified random sampling approach and dominant clay minerals were identified through XRD analysis. The absorption feature parameters like depth, width, area and asymmetry of the absorption peaks were derived from spectral profile of soil samples through DISPEC tool. The derived absorption feature parameters were used as inputs for modelling the dominant soil clay mineral present in the unknown samples using Random forest approach which resulted in kappa accuracy of 0.795. Besides, an attempt was made to classify the Hyperion data using Spectral Angle Mapper (SAM) algorithm with an overall accuracy of 68.43 %. Results showed that kaolinite was the dominant mineral present in the soils followed by montmorillonite in the study area.

[Research on characteristics of soil clay mineral evolution in paddy field and dry land by XRD spectrum].

Science.gov (United States)

Zhang, Zhi-dan; Li, Qiao; Luo, Xiang-li; Jiang, Hai-chao; Zheng, Qing-fu; Zhao, Lan-po; Wang, Ji-hong

2014-08-01

The present paper took the typical saline-alkali soil in Jilin province as study object, and determinated the soil clay mineral composition characteristics of soil in paddy field and dry land. Then XRD spectrum was used to analyze the evolutionary mechanism of clay mineral in the two kinds of soil. The results showed that the physical and chemical properties of soil in paddy field were better than those in dry land, and paddy field would promote the weathering of mineral particles in saline-alkali soil and enhance the silt content. Paddy field soil showed a strong potassium-removal process, with a higher degree of clay mineral hydration and lower degree of illite crystallinity. Analysis of XRD spectrum showed that the clay mineral composition was similar in two kinds of soil, while the intensity and position of diffraction peak showed difference. The evolution process of clay mineral in dry land was S/I mixture-->vermiculite, while in paddy field it was S/I mixture-->vermiculite-->kaolinite. One kind of hydroxylated 'chlorite' mineral would appear in saline-alkali soil in long-term cultivated paddy field. Taking into account that the physical and chemical properties of soil in paddy field were better then those in dry land, we could know that paddy field could help much improve soil structure, cultivate high-fertility soil and improve saline-alkali soil. This paper used XRD spectrum to determine the characteristics of clay minerals comprehensively, and analyzed two'kinds of land use comparatively, and was a new perspective of soil minerals study.

The Study of Abundance of Soil Minerals on Micro Toposequen of Karst Gunungsewu Pegunungan Selatan

Directory of Open Access Journals (Sweden)

Djoko Mulyanto

2008-05-01

Full Text Available Landform of Gunungsewu karst topography dominated by positive forms consists of hills and negative forms of dolines. On the micro toposequen of karst, most of dolines dominated by red soils which hue 2.5 YR – 5 YR, whereas on hills by soils which hue 5 YR – 7.5 YR. The aim of research was to study of soil minerals status on karst micro toposequent. Results showed that soil minerals of sand fraction on dolines dominated by quartz, opaque, and iron concretion, whereas on hills dominated by labradorite, and mafic minerals. Clay minerals on doline dominated by kaolinite whereas on hills by halloysite. The high concentration of kaolinite, quartz, opaque and iron concretions of soils on dolines appropriate with degree of soil weathering which in a line with decreasing of soil pH, silt/ clay ratio, and hue of soils on dolines redder than hue of soils on hills. The origin of soil parent material suggested come from volcanic materials.

Elevated moisture stimulates carbon loss from mineral soils by releasing protected organic matter.

Science.gov (United States)

Huang, Wenjuan; Hall, Steven J

2017-11-24

Moisture response functions for soil microbial carbon (C) mineralization remain a critical uncertainty for predicting ecosystem-climate feedbacks. Theory and models posit that C mineralization declines under elevated moisture and associated anaerobic conditions, leading to soil C accumulation. Yet, iron (Fe) reduction potentially releases protected C, providing an under-appreciated mechanism for C destabilization under elevated moisture. Here we incubate Mollisols from ecosystems under C 3 /C 4 plant rotations at moisture levels at and above field capacity over 5 months. Increased moisture and anaerobiosis initially suppress soil C mineralization, consistent with theory. However, after 25 days, elevated moisture stimulates cumulative gaseous C-loss as CO 2 and CH 4 to >150% of the control. Stable C isotopes show that mineralization of older C 3 -derived C released following Fe reduction dominates C losses. Counter to theory, elevated moisture may significantly accelerate C losses from mineral soils over weeks to months-a critical mechanistic deficiency of current Earth system models.

Improvement of nitrogen utilization and soil properties by addition of a mineral soil conditioner: mechanism and performance.

Science.gov (United States)

Yan, Xiaodan; Shi, Lin; Cai, Rumeng

2018-01-01

A mineral soil conditioner (MSC) composed of activated potash feldspar, gypsum, and calcium carbonate and containing an amount of available mineral nutrients, is shown to be effective for plant growth and acidic soil amelioration. In this study, a field test was conducted over four rice seasons by examining treatment with control check (CK), MSC, biological active carbon, and lime to investigate the nitrogen-use efficiency and mechanism of soil characteristic variations due to the desilicification and allitization of soil as well as the unrestrained use of nitrogen (N) fertilizer in recent years. Influences of MSC on the xylem sap intensity and mean rice yields were evaluated, and the soil type was also analyzed using the FactSage 6.1 Reaction, phase diagram, and Equilib modules. The results of the field trial showed that MSC application increased the xylem sap intensity and nitrogen export intensity by 37.33-39.85% and 31.40-51.20%, respectively. A significant increase (5.63-15.48%) in mean grain yields was achieved with MSC application over that with biological active carbon and lime application. The effects of MSC had a tendency to increase with time in the field experiment results, and grain yields increased after the initial application. The new formation of clay minerals exhibits a significant influence on [Formula: see text] fixation, especially for 2:1 phyllosilicates with illite, owing to the interlayers of the clay minerals. Our preliminary results showed that kaolinite, the main 1:1 phyllosilicate clay mineral in ferralsol, transformed to illite at room temperature as a consequence of the presence of H 4 SiO 4 and available K + supplied by MSC. This indicated that improving the soil quality combined with reducing N losses from soils is an efficient way to control non-point source pollution from agriculture without the risk of decreased in grain yield.

The distribution of selected elements and minerals in soil of the conterminous United States

Science.gov (United States)

Woodruff, Laurel G.; Cannon, William F.; Smith, David; Solano, Federico

2015-01-01

In 2007, the U.S. Geological Survey initiated a low-density (1 site per 1600 km2, 4857 sites) geochemical and mineralogical survey of soil of the conterminous United States as part of the North American Soil Geochemical Landscapes Project. Three soil samples were collected, if possible, from each site; (1) a sample from a depth of 0 to 5 cm, (2) a composite of the soil A-horizon, and (3) a deeper sample from the soil C-horizon or, if the top of the C-horizon was at a depth greater than 100 cm, from a depth of approximately 80–100 cm. The The major mineralogical components in samples from the soil A- and C-horizons were determined by a quantitative X-ray diffraction method using Rietveld refinement. Sampling ended in 2010 and chemical and mineralogical analyses were completed in May 2013. Maps of the conterminous United States showing predicted element and mineral concentrations were interpolated from actual soil data for each soil sample type by an inverse distance weighted (IDW) technique using ArcGIS software. Regional- and national-scale map patterns for selected elements and minerals apparent in interpolated maps are described here in the context of soil-forming factors and possible human inputs. These patterns can be related to (1) soil parent materials, for example, in the distribution of quartz, (2) climate impacts, for example, in the distribution of feldspar and kaolinite, (3) soil age, for example, in the distribution of carbonate in young glacial deposits, and (4) possible anthropogenic loading of phosphorus (P) and lead (Pb) to surface soil. This new geochemical and mineralogical data set for the conterminous United States represents a major step forward from prior national-scale soil geochemistry data and provides a robust soil data framework for the United States now and into the future.

The influence of site factors on nitrogen mineralization in forest soils ...

African Journals Online (AJOL)

The influence of site factors on nitrogen mineralization in forest soils of the ... on N mineralization, as well as the effect of N mineralization on forest productivity. ... of the natural log of mean annual temperature, geological substrate and total N ...

Runoff and windblown vehicle spray from road surfaces, risks and measures for soil and water.

NARCIS (Netherlands)

Schipper, P.N.M.; Comans, R.N.J.; Dijkstra, J.J.; Vergouwen, L.

2007-01-01

Soil and surface water along roads are exposed to pollution from motorways. The main pollutants are polycyclic aromatic hydrocarbons (PAH), mineral oil, heavy metals and salt. These pollutants originate from vehicles (fuel, wires, leakage), wear and degradation of road surfaces and road furniture

The mineralization and transformation of both added organic nitrogen and native soil N in red soils from four different ecological conditions

International Nuclear Information System (INIS)

Ye Qingfu; Zhang Qinzheng; He Zhenli; Xi Haifu; Wu Gang; Wilson, M.J.

1998-01-01

The NH 4 + -N, microbial biomass-N, humus-N, and extractable organic N derived from the added 15 N-labelled ryegrass and soil indigenous pool were measured separately with 15 N tracing techniques. Based on the recovery of NH 4 + - 15 N and lost- 15 N (mainly as NH 3 ), more than 30% of the added ryegrass 15 N was mineralized in 15 d. The amount of mineralized N increased with time up to 90 d for all soils except for the upland soil in which it decreased slightly. The mineralization of ryegrass N and incorporation of ryegrass- 15 N into microbial biomass was greatest in upland soil. The transformation of ryegrass 15 N into humus 15 N occurred rapidly in 15 d, with higher humus 15 N occurring in the upland or tea-garden soil than the paddy and unarable soil. The addition of ryegrass caused additional mineralization of soil indigenous organic N and enhanced the turnover of both microbial biomass N and stable organic N in soils

Interplay between black carbon and minerals contributes to long term carbon stabilization and mineral transformation

Science.gov (United States)

Liang, B.; Weng, Y. T.; Wang, C. C.; Chiang, C. C.; Liu, C. C.; Lehmann, J.

2017-12-01

Black carbon receives increasing global wide research attention due to its role in carbon sequestration, soil fertility enhancement and remediation application. Generally considered chemically stable in bulk, the reactive surface of BC can interplays with minerals and form strong chemical bondage, which renders physical protection of BC and contributes to its long term stabilization. Using historical BC-rich Amazonian Dark Earth (ADE), we probe the in-situ organo-mineral association and transformation of BC and minerals over a millennium scale using various synchrotron-based spectroscopic (XANES, FTIR) and microscopic (TXM) methods. Higher content of SRO minerals was found in BC-rich ADE compare to adjacent tropical soils. The iron signature found in BC-rich ADE was mainly ferrihydrite/lepidocrocite, a more reactive form of Fe compared to goethite, which was dominant in adjacent soil. Abundant nano minerals particles were observed in-situ associated with BC surface, in clusters and layers. The organo-mineral interaction lowers BC bioavailability and enhances its long-term stabilization in environment, while at the same time, transforms associated minerals into more reactive forms under rapid redox/weathering environment. The results suggest that mineral physical protection for BC sequestration may be more important than previous understanding. The scale up application of BC/biochar into agricultural systems and natural environments have long lasting impact on the in-situ transformation of associated minerals.

Carbon and nitrogen mineralization in vineyard acid soils amended with a bentonitic winery waste

Science.gov (United States)

Fernández-Calviño, David; Rodríguez-Salgado, Isabel; Pérez-Rodríguez, Paula; Díaz-Raviña, Montserrat; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel

2015-04-01

Carbon mineralization and nitrogen ammonification processes were determined in different vineyard soils. The measurements were performed in samples non-amended and amended with different bentonitic winery waste concentrations. Carbon mineralization was measured as CO2 released by the soil under laboratory conditions, whereas NH4+ was determined after its extraction with KCl 2M. The time evolution of both, carbon mineralization and nitrogen ammonification, was followed during 42 days. The released CO2 was low in the analyzed vineyard soils, and hence the metabolic activity in these soils was low. The addition of the bentonitic winery waste to the studied soils increased highly the carbon mineralization (2-5 fold), showing that the organic matter added together the bentonitic waste to the soil have low stability. In both cases, amended and non-amended samples, the maximum carbon mineralization was measured during the first days (2-4 days), decreasing as the incubation time increased. The NH4+ results showed an important effect of bentonitic winery waste on the ammonification behavior in the studied soils. In the non-amended samples the ammonification was no detected in none of the soils, whereas in the amended soils important NH4+ concentrations were detected. In these cases, the ammonification was fast, reaching the maximum values of NH4 between 7 and 14 days after the bentonitic waste additions. Also, the percentages of ammonification respect to the total nitrogen in the soil were high, showing that the nitrogen provided by the bentonitic waste to the soil is non-stable. The fast carbon mineralization found in the soils amended with bentonitic winery wastes shows low possibilities of the use of this waste for the increasing the organic carbon pools in the soil.On the other hand, the use of this waste as N-fertilizer can be possible. However, due its fast ammonification, the waste should be added to the soils during active plant growth periods.

Physiochemical Influence of Soil Minerals on the Organic Reduction of Soil Chromium

International Nuclear Information System (INIS)

Njoku, P.C.; Nweze, C.A.

2009-01-01

The physiochemical influence of soil minerals (Bentonite, Kaolinite, Diatomite,Rutile and Ferrihydrite) on the organic reduction ofchromium (VI) has been investigated with Oxalic acid as the organic reductant. The effect of pH and particle sizes of the soil minerals were also investigated. Results showed that with 0.1mol/dm3 concentration of Oxalic acid, the concentration of chromium(VI) remaining was 0.28, 0.34,0.38, 0.46 and 0.52mg/kgfor Bentonite, Rutile, Diatomite, Kaolinite and Ferrihydrite respectively whereas at 0.5mol/dm3of oxalic acid, the concentration of chromium reduced to 0.20,0.26, 0.30, 0.38, and0.44mg/kg for Bentonite, Rutile, Diatomite, Kaolinite and Ferrihydrite. Increasedconcentration of oxalic acid increased the reduction of chromium(VI) to chromium(III). At pH 5.0, the concentration of chromium(VI)left was 0.28, 0.34, 0.38,0.46 and 0.52mg/kg forBentonite, Rutile, Diatomite, Kaolinite and Ferrihydrite while at pH 2.5, concentration was0.16, 0.22, 0.26, 0.34 and 0.43mg/kg respectively. At particle size of 47-42 microns, concentration of chromium(VI) was 0.28, 0.34,0.38, 0.46, 0.52mg/kg for the same order ofthe soil minerals. At micron sizes of33-29 and 28-25 ranges the concentration ofchromium(VI) left was 0.23, 0.29, 0.33,0.41 and 0.47mg/kg for both micron sizes and corresponding minerals as well. These results showed that above 33-29 micron sizes, the influence of particle size was negligible. (author)

Picloram and Aminopyralid Sorption to Soil and Clay Minerals

Science.gov (United States)

Aminopyralid sorption data are lacking, and these data are needed to predict off-target transport and plant available herbicide in soil solution. The objective of this research was to determine the sorption of picloram and aminopyralid to five soils and three clay minerals and determine if the pote...

Thermomagnetic identification of manganese and iron minerals present in soils and industrial dusts

Science.gov (United States)

Wawer, Małgorzata; Rachwał, Marzena; Jabłońska, Mariola; Krzykawski, Tomasz; Magiera, Tadeusz

2017-04-01

Many industries (e.g. metallurgy, power, cement, and coking plants) constitute a sources of industrial dusts containing technogenic magnetic particles (TMP). TMP are mostly iron oxides with ferrimagnetic or antiferromagnetic properties, therefore their presence in dusts, soils and sediments can be easily detected by magnetic susceptibility measurements. TMP, thanks their specific mineral and magnetic properties, and well developed specific surface area, are characterized by a chemical affinity for some elements like heavy metals. The main objective of this study was identification of manganese and iron (hydro)oxides occurring in industrial dusts and soils being under their deposition for long time period. In principle, Mn and Fe (hydro)oxides present in these samples originate from high-temperature technological processes. Soils samples (collected from different soil horizons) taken from surroundings of power station, iron/steel and non-ferrous plants as well as metallurgical dusts and fly ashes from power stations were subjected to investigation. During the studies temperature dependent magnetic susceptibility measurements and X-ray powder diffraction analyses were applied. Thermomagnetic analyses (K-T) revealed differences between samples from particular industries, however an inflexion at 450-500°C of all curves was observed indicating a probable occurrence of maghemite- or titanomagnetite-like phases. The curves of TMP emitted by power plants have inflection at 580 °C indicating that magnetite was the main magnetic phase. In case of TMP originated from non-ferrous metal smelting additional curve deflection at 130 and 210 °C occurred relating to intermediate titanomagnetite or iron sulfides. X-ray diffraction proved the occurrence of magnetite and maghemite in almost all samples, especially connected with power industry and iron/steel metallurgy. Mineral analysis revealed that kind of industrial process influenced on the dominating mineral forms found in

Linking annual N2O emission in organic soils to mineral nitrogen input as estimated by heterotrophic respiration and soil C/N ratio.

Science.gov (United States)

Mu, Zhijian; Huang, Aiying; Ni, Jiupai; Xie, Deti

2014-01-01

Organic soils are an important source of N2O, but global estimates of these fluxes remain uncertain because measurements are sparse. We tested the hypothesis that N2O fluxes can be predicted from estimates of mineral nitrogen input, calculated from readily-available measurements of CO2 flux and soil C/N ratio. From studies of organic soils throughout the world, we compiled a data set of annual CO2 and N2O fluxes which were measured concurrently. The input of soil mineral nitrogen in these studies was estimated from applied fertilizer nitrogen and organic nitrogen mineralization. The latter was calculated by dividing the rate of soil heterotrophic respiration by soil C/N ratio. This index of mineral nitrogen input explained up to 69% of the overall variability of N2O fluxes, whereas CO2 flux or soil C/N ratio alone explained only 49% and 36% of the variability, respectively. Including water table level in the model, along with mineral nitrogen input, further improved the model with the explanatory proportion of variability in N2O flux increasing to 75%. Unlike grassland or cropland soils, forest soils were evidently nitrogen-limited, so water table level had no significant effect on N2O flux. Our proposed approach, which uses the product of soil-derived CO2 flux and the inverse of soil C/N ratio as a proxy for nitrogen mineralization, shows promise for estimating regional or global N2O fluxes from organic soils, although some further enhancements may be warranted.

Arabian Red Sea coastal soils as potential mineral dust sources

KAUST Repository

Prakash, P. Jish; Stenchikov, Georgiy L.; Tao, Weichun; Yapici, Tahir; Warsama, Bashir H.; Engelbrecht, Johann

2016-01-01

, because of its proximity, directly affects the Red Sea and coastal urban centers. The potential of soils to be suspended as airborne mineral dust depends largely on soil texture, moisture content and particle size distributions. Airborne dust inevitably

Carbon Footprint of Biofuel Sugarcane Produced in Mineral and Organic Soils in Florida

Energy Technology Data Exchange (ETDEWEB)

Izursa, Jose-Luis; Hanlon, Edward; Amponsah, Nana; Capece, John

2013-02-06

Ethanol produced from sugarcane is an existing and accessible form of renewable energy. In this study, we applied the Life Cycle Assessment (LCA) approach to estimate the Carbon Footprint (CFP) of biofuel sugarcane produced on mineral (sandy) and organic (muck) soils in Florida. CFP was estimated from greenhouse gas (GHG) emissions (CO2, CH4, and N2O) during the biofuel sugarcane cultivation. The data for the energy (fossil fuels and electricity), equipment, and chemical fertilizers were taken from enterprise budgets prepared by the University of Florida based on surveys and interviews obtained from local growers during the cropping years 2007/2008 and 2009/2010 for mineral soils and 2008/2009 for organic soils. Emissions from biomass burning and organic land use were calculated based on the IPCC guidelines. The results show that the CFP for biofuel sugarcane production is 0.04 kg CO2e kg-1y-1 when produced in mineral soils and 0.46 kg CO2e kg-1y-1 when produced in organic soils. Most of the GHG emissions from production of biofuel sugarcane in mineral soils come from equipment (33%), fertilizers (28%), and biomass burning (27%); whereas GHG emissions from production in organic soils come predominantly from the soil (93%). This difference should be considered to adopt new practices for a more sustainable farming system if biofuel feedstocks are to be considered.

The solonetzic process in surface soils and buried paleosols and its reflection in the mineralogical soil memory

Science.gov (United States)

Chizhikova, N. P.; Kovda, I. V.; Borisov, A. V.; Shishlina, N. I.

2009-10-01

The development of the solonetzic process in paleosols buried under kurgans and in the modern surface soils has been studied on the basis of the analysis of the clay (memory“ of the solid-phase soil components. The mineralogical characteristics show that the solonetzic process in the modern background soil is more developed. The mineralogical approach allows us to reveal the long-term changes in the soil status; it is less useful for studying the effect of short-term bioclimatic fluctuations. In the latter case, more labile soil characteristics should be used. The mineralogical method, combined with other methods, becomes more informative upon the study of soil chronosequences. Our studies have shown that the data on the clay minerals in the buried paleosols may contain specific information useful for paleoreconstructions that is not provided by other methods.

Anisotropic surface chemistry properties and adsorption behavior of silicate mineral crystals.

Science.gov (United States)

Xu, Longhua; Tian, Jia; Wu, Houqin; Fang, Shuai; Lu, Zhongyuan; Ma, Caifeng; Sun, Wei; Hu, Yuehua

2018-03-07

Anisotropic surface properties of minerals play an important role in a variety of fields. With a focus on the two most intensively investigated silicate minerals (i.e., phyllosilicate minerals and pegmatite aluminosilicate minerals), this review highlights the research on their anisotropic surface properties based on their crystal structures. Four surface features comprise the anisotropic surface chemistry of minerals: broken bonds, energy, wettability, and charge. Analysis of surface broken bond and energy anisotropy helps to explain the cleavage and growth properties of mineral crystals, and understanding surface wettability and charge anisotropy is critical to the analysis of minerals' solution behavior, such as their flotation performance and rheological properties. In a specific reaction, the anisotropic surface properties of minerals are reflected in the adsorption strengths of reagents on different mineral surfaces. Combined with the knowledge of mineral crushing and grinding, a thorough understanding of the anisotropic surface chemistry properties and the anisotropic adsorption behavior of minerals will lead to the development of effective relational models comprising their crystal structure, surface chemistry properties, and targeted reagent adsorption. Overall, such a comprehensive approach is expected to firmly establish the connection between selective cleavage of mineral crystals for desired surfaces and designing novel reagents selectively adsorbed on the mineral surfaces. As tools to characterize the anisotropic surface chemistry properties of minerals, DLVO theory, atomic force microscopy (AFM), and molecular dynamics (MD) simulations are also reviewed. Copyright © 2017 Elsevier B.V. All rights reserved.

Determination of total organic phosphorus in samples of mineral soils

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Armi Kaila

1962-01-01

Full Text Available In this paper some observations on the estimation of organic phosphorus in mineral soils are reported. The fact is emphasized that the accuracy of all the methods available is relatively poor. Usually, there are no reasons to pay attention to differences less than about 20 ppm. of organic P. Analyses performed on 345 samples of Finnish mineral soils by the extraction method of MEHTA et. al. (10 and by a simple procedure adopted by the author (successive extractions with 4 N H2SO4 and 0.5 N NaOH at room temperature in the ratio of 1 to 100 gave, on the average, equal results. It seemed to be likely that the MEHTA method removed the organic phosphorus more completely than did the less vigorous method, but in the former the partial hydrolysis of organic phosphorus compounds tends to be higher than in the latter. An attempt was made to find out whether the differences between the respective values for organic phosphorus obtained by an ignition method and the simple extraction method could be connected with any characteristics of the soil. No correlation or only a low correlation coefficient could be calculated between the difference in the results of these two methods and e. g. the pH-value, the content of clay, organic carbon, aluminium and iron soluble in Tamm’s acid oxalate, the indicator of the phosphate sorption capacity, or the »Fe-bound» inorganic phosphorus, respectively. The absolute difference tended to increase with an increase in the content of organic phosphorus. For the 250 samples of surface soils analyzed, the ignition method gave values which were, on the average, about 50 ppm. higher than the results obtained by the extraction procedure. The corresponding difference for the 120 samples from deeper layers was about 20 ppm of organic P. The author recommends, for the present, the determination of the total soil organic phosphorus as an average of the results obtained by the ignition method and the extraction method.

Use of Coffee Pulp and Minerals for Natural Soil Ameliorant

Directory of Open Access Journals (Sweden)

Pujiyanto Pujiyanto

2007-05-01

Full Text Available In coffee plantation, solid waste of coffee pulp is usually collected as heap nearby processing facilities for several months prior being used as compost. The practice is leading to the formation of odor and liquid which contaminate the environment. Experiments to evaluate the effect of natural soil ameliorant derived from coffee pulp and minerals were conducted at The Indonesian Coffee and Cocoa Research Institute in Jember, East Java. The experiments were intended to optimize the use of coffee pulp to support farming sustainability and minimize negative impacts of solid waste disposal originated from coffee cherry processing. Prior to applications, coffee pulp was hulled to organic paste. The paste was then mixed with 10% minerals (b/b. Composition of the minerals was 50% zeolite and 50% rock phosphate powder. The ameliorant was characterized for their physical and chemical properties. Agronomic tests were conducted on coffee and cocoa seedling. The experiments were arranged according to Randomized Completely Design with 2 factors, consisted of natural ameliorant and inorganic fertilizer respectively. Natural ameliorant derived from coffee pulp was applied at 6 levels: 0, 30, 60, 90, 120 and 150 g dry ameliorant/seedling of 3 kg soil, equivalent to 0, 1, 2, 3, 4 and 5% (b/b of ameliorant respectively. Inorganic fertilizer was applied at 2 levels: 0 and 2 g fertilizer/application of N-P-K compound fertilizer of 15-15-15 respectively. The inorganic fertilizer was applied 4 times during nursery of coffee and cocoa. The result of the experiment indicated that coffee pulp may be used as natural soil ameliorant. Composition of ameliorant of 90% coffee pulp and 10% of minerals has good physical and chemical characteristics for soil amelioration. The composition has high water holding capacity; cations exchange capacity, organic carbon and phosphorus contents which are favorable to increase soil capacity to support plant growth. Application of

Soil phosphorus redistribution among iron-bearing minerals under redox fluctuation

Science.gov (United States)

Lin, Y.; Bhattacharyya, A.; Campbell, A.; Nico, P. S.; Pett-Ridge, J.; Silver, W. L.

2016-12-01

Phosphorus (P) is a key limiting nutrient in tropical forests that governs primary production, litter decomposition, and soil respiration. A large proportion of P in these highly weathered soils is bound to short-range ordered or poorly crystalline iron (Fe) minerals. It is well-documented that these Fe minerals are redox-sensitive; however, little is known about how Fe-redox interactions affect soil P turnover. We evaluated the impacts of oxic/anoxic fluctuation on soil P fractions and reactive Fe species in a laboratory incubation experiment. Soils from a humid tropical forest were amended with plant biomass and incubated for up to 44 days under four redox regimes: static oxic, static anoxic, high frequency fluctuating (4-day oxic/4-day anoxic), and low frequency fluctuating (8-day oxic/4-day anoxic). We found that the static anoxic treatment induced a 10-fold increase in Fe(II) (extracted by hydrochloric acid) and a 1.5-fold increase in poorly crystalline Fe (extracted by ammonium oxalate), suggesting that anoxic conditions drastically increased Fe(III) reduction and the formation of amorphous Fe minerals. Static anoxic conditions also increased Fe-bound P (extracted by sodium hydroxide) and increased the oxalate-extractable P by up to 110% relative to static oxic conditions. In two fluctuating treatments, Fe(II) and oxalate-extractable Fe and P were all increased by short-term reduction events after 30 minutes, but fell back to their initial levels after 3 hours. These results suggest that reductive dissolution of Fe(III) minerals mobilized a significant amount of P; however, this P could be rapidly re-adsorbed. Furthermore, bioavailable P extracted by sodium bicarbonate solution was largely unaffected by redox regimes and was only increased by static anoxic conditions after 20 days. Overall, our data demonstrate that a significant amount of soil P may be liberated and re-adsorbed by Fe minerals during redox fluctuation. Even though bioavailable P appears to be

Quantification of centimeter-scale spatial variation in PAH, glucose and benzoic acid mineralization and soil organic matter in road-side soil

Energy Technology Data Exchange (ETDEWEB)

Hybholt, Trine K.; Aamand, Jens [Department of Geochemistry, Geological Survey of Denmark and Greenland (GEUS), Oster Voldgade 10, DK-1350 Copenhagen K (Denmark); Johnsen, Anders R., E-mail: arj@geus.dk [Department of Geochemistry, Geological Survey of Denmark and Greenland (GEUS), Oster Voldgade 10, DK-1350 Copenhagen K (Denmark)

2011-05-15

The aim of the study was to determine centimeter-scale spatial variation in mineralization potential in diffusely polluted soil. To this end we employed a 96-well microplate method to measure the mineralization of {sup 14}C-labeled organic compounds in deep-well microplates and thereby compile mineralization curves for 348 soil samples of 0.2-cm{sup 3}. Centimeter-scale spatial variation in organic matter and the mineralization of glucose, benzoic acid, and PAHs (phenanthrene and pyrene) was determined for urban road-side soil sampled as arrays (7 x 11 cm) of 96 subsamples. The spatial variation in mineralization was visualized by means of 2-D contour maps and quantified by means of semivariograms. The geostatistical analysis showed that the easily degradable compounds (glucose and benzoic acid) exhibited little spatial variation in mineralization potential, whereas the mineralization was highly heterogeneous for the PAH compounds that require specialized degraders. The spatial heterogeneity should be taken into account when estimating natural attenuation rates. - Highlights: > Geostatistics were applied at the centimeter scale. > Glucose and benzoic acid mineralization showed little spatial variation. > PAH mineralization was highly variable at the sub-centimeter scale. > High spatial heterogeneity may be caused by low functional redundancy. - This study supports the hypothesis that specialized xenobiotic degraders may show high spatial heterogeneity in soil due to low functional redundancy.

Soft X-ray spectromicroscopy study of mineral-organic matter associations in pasture soil clay fractions.

Science.gov (United States)

Chen, Chunmei; Dynes, James J; Wang, Jian; Karunakaran, Chithra; Sparks, Donald L

2014-06-17

There is a growing acceptance that associations with soil minerals may be the most important overarching stabilization mechanism for soil organic matter. However, direct investigation of organo-mineral associations has been hampered by a lack of methods that can simultaneously characterize organic matter (OM) and soil minerals. In this study, STXM-NEXAFS spectroscopy at the C 1s, Ca 2p, Fe 2p, Al 1s, and Si 1s edges was used to investigate C associations with Ca, Fe, Al, and Si species in soil clay fractions from an upland pasture hillslope. Bulk techniques including C and N NEXAFS, Fe K-edge EXAFS spectroscopy, and XRD were applied to provide additional information. Results demonstrated that C was associated with Ca, Fe, Al, and Si with no separate phase in soil clay particles. In soil clay particles, the pervasive C forms were aromatic C, carboxyl C, and polysaccharides with the relative abundance of carboxyl C and polysaccharides varying spatially at the submicrometer scale. Only limited regions in the soil clay particles had aliphatic C. Good C-Ca spatial correlations were found for soil clay particles with no CaCO3, suggesting a strong role of Ca in organo-mineral assemblage formation. Fe EXAFS showed that about 50% of the total Fe in soils was contained in Fe oxides, whereas Fe-bearing aluminosilicates (vermiculite and Illite) accounted for another 50%. Fe oxides in the soil were mainly crystalline goethite and hematite, with lesser amounts of poorly crystalline ferrihydrite. XRD revealed that soil clay aluminosilicates were hydroxy-interlayered vermiculite, Illite, and kaolinite. C showed similar correlation with Fe to Al and Si, implying a similar association of Fe oxides and aluminosilicates with organic matter in organo-mineral associations. These direct microscopic determinations can help improve understanding of organo-mineral interactions in soils.

Internal reflection spectroscopic analysis of sulphide mineral surfaces

International Nuclear Information System (INIS)

Kaoma, J.

1989-01-01

To establish the reason for flotation of sulfide minerals in the absence of any conventional collector, internal reflection spectroscopic analysis (IRS) of their surfaces was conducted. sulfur, sulfates, thiosulfates, and hydrocarbonates have been detected on the surface of as-grand sulfide minerals. On sodium sulfide-treated surfaces, both sulfur and polysulfide have also been found to be present. From these findings, the flotation of sulfide minerals without collectors is discussed. (author). 26 refs

Molecular analysis of manufactured gas plant soils for naphthalene mineralization

International Nuclear Information System (INIS)

Sanseverino, J.; Werner, C.; Fleming, J.; Applegate, B.M.; King, J.M.H.; Sayler, G.S.; Blackburn, J.

1991-01-01

New molecular tools are being developed and tested to ascertain the biodegradability of hazardous wastes by soil bacterial population. The potential for manufactured gas plant (MGP) soil bacterial populations to degrade naphthalene, as a component mixture of polynuclear aromatic hydrocarbons, was evaluated by the detection of a naphthalene biodegradative genotype by DNA probe hybridization with DNA extracts and colonies of cultured bacteria of the MGP soils. The activity of the naphthalene-degrading populations was evaluated by mineralization assays, 14 CO 2 production from 14 C-naphthalene. Direct messenger RNA (mRNA) extraction from MGP soil was evaluated as an instantaneous measure of naphthalene catabolic gene expression in MGP soil. The bioavailability of naphthalene for bacterial degradation within the MGP soils was assessed by measuring the bioluminescent response of a naphthalene-lux catabolic reporter strain Pseudomonas fluorescens HK44 (pUTK21). DNA extracted from 5 MGP soils and 1 creosote-contaminated soil and hybridized with a nahA gene probe indicated that the naphthalene degradative genes were present in all samples in the range of 0.06 to 0.95 ng/100 μl DNA extract which was calculated to represent 3.58 x 10 8 to 1.05 x 10 10 nahA positive cells/g soil. Phenanthrene, anthracene, and benzo(a)pyrene were mineralized also by some of the soils. NAH7 homologous messenger RNA transcripts were detectable in one MGP soil and in the creosote-contaminated soil

Sulfide Mineral Surfaces

International Nuclear Information System (INIS)

Rosso, Kevin M.; Vaughan, David J.

2006-01-01

The past twenty years or so have seen dramatic development of the experimental and theoretical tools available to study the surfaces of solids at the molecular (?atomic resolution?) scale. On the experimental side, two areas of development well illustrate these advances. The first concerns the high intensity photon sources associated with synchrotron radiation; these have both greatly improved the surface sensitivity and spatial resolution of already established surface spectroscopic and diffraction methods, and enabled the development of new methods for studying surfaces. The second centers on the scanning probe microscopy (SPM) techniques initially developed in the 1980's with the first scanning tunneling microscope (STM) and atomic force microscope (AFM) experiments. The direct 'observation' of individual atoms at surfaces made possible with these methods has truly revolutionized surface science. On the theoretical side, the availability of high performance computers coupled with advances in computational modeling has provided powerful new tools to complement the advances in experiment. Particularly important have been the quantum mechanics based computational approaches such as density functional theory (DFT), which can now be easily used to calculate the equilibrium crystal structures of solids and surfaces from first principles, and to provide insights into their electronic structure. In this chapter, we review current knowledge of sulfide mineral surfaces, beginning with an overview of the principles relevant to the study of the surfaces of all crystalline solids. This includes the thermodynamics of surfaces, the atomic structure of surfaces (surface crystallography and structural stability, adjustments of atoms at the surface through relaxation or reconstruction, surface defects) and the electronic structure of surfaces. We then discuss examples where specific crystal surfaces have been studied, with the main sulfide minerals organized by structure type

Sulfide Mineral Surfaces

Energy Technology Data Exchange (ETDEWEB)

Rosso, Kevin M.; Vaughan, David J.

2006-08-01

The past twenty years or so have seen dramatic development of the experimental and theoretical tools available to study the surfaces of solids at the molecular (?atomic resolution?) scale. On the experimental side, two areas of development well illustrate these advances. The first concerns the high intensity photon sources associated with synchrotron radiation; these have both greatly improved the surface sensitivity and spatial resolution of already established surface spectroscopic and diffraction methods, and enabled the development of new methods for studying surfaces. The second centers on the scanning probe microscopy (SPM) techniques initially developed in the 1980's with the first scanning tunneling microscope (STM) and atomic force microscope (AFM) experiments. The direct 'observation' of individual atoms at surfaces made possible with these methods has truly revolutionized surface science. On the theoretical side, the availability of high performance computers coupled with advances in computational modeling has provided powerful new tools to complement the advances in experiment. Particularly important have been the quantum mechanics based computational approaches such as density functional theory (DFT), which can now be easily used to calculate the equilibrium crystal structures of solids and surfaces from first principles, and to provide insights into their electronic structure. In this chapter, we review current knowledge of sulfide mineral surfaces, beginning with an overview of the principles relevant to the study of the surfaces of all crystalline solids. This includes the thermodynamics of surfaces, the atomic structure of surfaces (surface crystallography and structural stability, adjustments of atoms at the surface through relaxation or reconstruction, surface defects) and the electronic structure of surfaces. We then discuss examples where specific crystal surfaces have been studied, with the main sulfide minerals organized by

Instrumental neutron activation analysis as a tool for assessing the solubility of soil mineral matter in strong acid

International Nuclear Information System (INIS)

Steinnes, E.; Naeumann, R.

2004-01-01

Fifty samples of natural surface soils with high but variable organic matter content were analyzed for 13 elements (Na, Al, K, Sc, V, Cr, Mn, Fe, Co, Zn, Sr, Ba, La) by INAA. The same samples were analyzed for the 'total-recoverable' fraction of these elements by ICP-OES after decomposition with 7M HNO 3 , and the results are compared. The data are discussed separately for two groups of samples with organic matter contents of respectively >80% and Mn (77)>La (60)>Fe = Zn (53)>V (33)>Cr (29)>Sc (25)>Al = Ba (17)>Sr (13)>K (5)>Na (2). The results are in good agreement with corresponding literature data for mineral soils in the case of Al, K, Sc, V, Cr, Fe, and La. In the case of Na, Mn, Co, Zn, Sr, and Ba the present surface soils showed significantly higher 'total-recoverable' fractions than the previously studied subsoils. Possible reasons for these differences are discussed. INAA remains a convenient reference technique for determination of total concentrations with the rapidly increasing use of strong mineral acids in environmental studies of elements. (author)

Plant litter chemistry alters the content and composition of organic carbon associated with soil mineral and aggregate fractions in invaded ecosystems.

Science.gov (United States)

Tamura, Mioko; Suseela, Vidya; Simpson, Myrna; Powell, Brian; Tharayil, Nishanth

2017-10-01

the higher surface area of soil minerals at this site. The plant biomarkers were lower in the aggregate fractions of the P. lobata-invaded soils, compared with noninvaded pine stands, potentially suggesting a microbial co-metabolism of pine-derived compounds. These results highlight the complex interactions among litter chemistry, soil biota, and minerals in mediating soil C storage in unmanaged ecosystems; these interactions are particularly important under global changes that may alter plant species composition and hence the quantity and chemistry of litter inputs in terrestrial ecosystems. © 2017 John Wiley & Sons Ltd.

Banana leaf and glucose mineralization and soil organic matter in microhabitats of banana plantations under long-term pesticide use.

Science.gov (United States)

Blume, Elena; Reichert, José Miguel

2015-06-01

Soil organic matter (SOM) and microbial activity are key components of soil quality and sustainability. In the humid tropics of Costa Rica 3 pesticide regimes were studied-fungicide (low input); fungicide and herbicide (medium input); and fungicide, herbicide, and nematicide (high input)-under continuous banana cultivation for 5 yr (young) or 20 yr (old) in 3 microhabitats-nematicide ring around plants, litter pile of harvested banana, and bare area between litter pile and nematicide ring. Soil samples were incubated sequentially in the laboratory: unamended, amended with glucose, and amended with ground banana leaves. Soil organic matter varied with microhabitat, being greatest in the litter pile, where microbes had the greatest basal respiration with ground banana leaf, whereas microbes in the nematicide ring had the greatest respiration with glucose. These results suggest that soil microbes adapt to specific microhabitats. Young banana plantations had similar SOM compared with old plantations, but the former had greater basal microbial respiration in unamended and in glucose-amended soil and greater first-order mineralization rates in glucose-amended soil, thus indicating soil biological quality decline over time. High pesticide input did not decrease microbial activity or mineralization rate in surface soil. In conclusion, microbial activity in tropical volcanic soil is highly adaptable to organic and inorganic inputs. © 2015 SETAC.

Impact of activated carbon, biochar and compost on the desorption and mineralization of phenanthrene in soil

International Nuclear Information System (INIS)

Marchal, Geoffrey; Smith, Kilian E.C.; Rein, Arno; Winding, Anne; Wollensen de Jonge, Lis; Trapp, Stefan; Karlson, Ulrich G.

2013-01-01

Sorption of PAHs to carbonaceous soil amendments reduces their dissolved concentrations, limiting toxicity but also potentially biodegradation. Therefore, the maximum abiotic desorption of freshly sorbed phenanthrene (≤5 mg kg −1 ) was measured in three soils amended with activated carbon (AC), biochar or compost. Total amounts of phenanthrene desorbed were similar between the different soils, but the amendment type had a large influence. Complete desorption was observed in the unamended and compost amended soils, but this reduced for biochar (41% desorbed) and AC (8% desorbed). Cumulative amounts mineralized were 28% for the unamended control, 19% for compost, 13% for biochar and 4% for AC. Therefore, the effects of the amendments in soil in reducing desorption were also reflected in the extents of mineralization. Modeling was used to analyze key processes, indicating that for the AC and charcoal treatments bacterial activity did not limit mineralization, but rather desorption into the dissolved phase. -- Highlights: •Phenanthrene desorption and mineralization compared in soils with activated carbon, charcoal or compost. •Only activated charcoal and biochar hindered both desorption and mineralization. •A linear relationship was found between the extents desorbed and mineralized. •Modelling indicated that bacterial activity was not limiting but that desorption was. -- Extraction into an exhaustive silicone sink measures the maximum phenanthrene desorption from soils with amendments, and this is reflected in the extent of mineralization

Soil mineral assemblage influences on microbial communities and carbon cycling under fresh organic matter input

Science.gov (United States)

Finley, B. K.; Schwartz, E.; Koch, B.; Dijkstra, P.; Hungate, B. A.

2017-12-01

The interactions between soil mineral assemblages and microbial communities are important drivers of soil organic carbon (SOC) cycling and storage, although the mechanisms driving these interactions remain unclear. There is increasing evidence supporting the importance of associations with poorly crystalline, short-range order (SRO) minerals in protection of SOC from microbial utilization. However, how the microbial processing of SRO-associated SOC may be influenced by fresh organic matter inputs (priming) remains poorly understood. The influence on SRO minerals on soil microbial community dynamics is uncertain as well. Therefore, we conducted a priming incubation by adding either a simulated root exudate mixture or conifer needle litter to three soils from a mixed-conifer ecosystem. The parent material of the soils were andesite, basalt, and granite and decreased in SRO mineral content, respectively. We also conducted a parallel quantitative stable isotope probing incubation by adding 18O-labelled water to the soils to isotopically label microbial DNA in situ. This allowed us to characterize and identify the active bacterial and archaeal community and taxon-specific growth under fresh organic matter input. While the granite soil (lowest SRO content), had the largest total mineralization, the least priming occurred. The andesite and basalt soils (greater SRO content) had lower total respiration, but greater priming. Across all treatments, the granite soil, while having the lowest species richness of the entire community (249 taxa, both active and inactive), had a larger active community (90%) in response to new SOC input. The andesite and basalt soils, while having greater total species richness of the entire community at 333 and 325 taxa, respectively, had fewer active taxa in response to new C compared to the granite soil (30% and 49% taxa, respectively). These findings suggest that the soil mineral assemblage is an important driver on SOC cycling under fresh

Mineralization of 14C-labelled aromatic pesticide molecules in Egyptian soils under aerobic and anaerobic conditions

International Nuclear Information System (INIS)

Zayed, S.M.A.D.; Earghaly, M.; Mahdy, F.; El-Maghraby, S.; Taha, H.; Soliman, S.M.

2001-01-01

The mineralization of 2,4-D, carbofuran and pirimiphos-methyl in Egyptian soils was studied over a period of 90 days. Laboratory studies under aerobic and anaerobic conditions were conducted using 14 C-ring labelled pesticides. Under anaerobic conditions 10-14% of applied ring labelled 2,4-D mineralized during 90 days with no significant variations due to soil type. Under aerobic conditions, 2,4-D mineralized more readily in clay soil to reach 29-34% of applied dose within 90 days. In clay loam soil, 14 C-carbofuran and 14 C-pirimiphos-methyl mineralized at a rather slow rate to reach 12-14% and 12-13% of applied dose in 90 days, respectively under aerobic conditions. Generally, soils repeatedly treated with pesticides gave a slightly lower percentage of mineralization than control soils. In all studies, the soil extractable pesticide residues decreased with time and the bound residues gradually increased. The highest binding affinity of about 26-29% was observed with 2,4-D in clay soil under aerobic conditions in 90 days. Carbofuran, and pirimiphos-methyl, on the other hand, had lower binding capacity that did not exceed 16% of applied radioactivity. (author)

Chemical and Physical Interactions of Martian Surface Material

Science.gov (United States)

Bishop, J. L.

1999-09-01

A model of alteration and maturation of the Martian surface material is described involving both chemical and physical interactions. Physical processes involve distribution and mixing of the fine-grained soil particles across the surface and into the atmosphere. Chemical processes include reaction of sulfate, salt and oxidizing components of the soil particles; these agents in the soils deposited on rocks will chew through the rock minerals forming coatings and will bind surface soils together to form duricrust deposits. Formation of crystalline iron oxide/oxyhydroxide minerals through hydrothermal processes and of poorly crystalline and amorphous phases through palagonitic processes both contribute to formation of the soil particles. Chemical and physical alteration of these soil minerals and phases contribute to producing the chemical, magnetic and spectroscopic character of the Martian soil as observed by Mars Pathfinder and Mars Global Surveyor. Minerals such as maghemite/magnetite and jarosite/alunite have been observed in terrestrial volcanic soils near steam vents and may be important components of the Martian surface material. The spectroscopic properties of several terrestrial volcanic soils containing these minerals have been analyzed and evaluated in terms of the spectroscopic character of the surface material on Mars.

Temporal and spatial dynamics of mineral levels of forage, soil and ...

African Journals Online (AJOL)

Temporal and spatial dynamics of mineral levels of forage, soil and cattle blood ... In the plain lands, local variations occurred for soil phosphorus and magnesium. ... Rangeland improvement and supplementation strategies are suggested to ...

Mineral oil residues in soil and apple under temperate conditions of Kashmir, India.

Science.gov (United States)

Ahmad, Malik Mukhtar; Wani, Ashraf Alam; Sofi, Mubashir; Ara, Ishrat

2018-03-09

The study was undertaken to ascertain the persistence of Orchol-13, a mineral oil used against insect pests of horticultural fruit crops in soil and apple following the dormant and summer applications of 2 and 0.75% respectively. Soil samples were collected during dormant, while as both soil and apple samples were collected during summer season. Samples were collected at 0, 1, 3, and 5 days post treatment in both the seasons. Average recoveries of paraffinic constituents (which constitute about 60% of mineral oils by composition) from soil and apple at 1 μg ml -1 spiking level were found to be 74.18 and 76.81% respectively. The final quantification of paraffinic constituents was performed on gas chromatograph equipped with flame ionization detector (GC-FID). No paraffinic constituents of mineral oil could be detected in soil and apple at 0 day post treatment in both the seasons.

Effect of clay minerals on the stabilization of black cotton and lateritic soils

International Nuclear Information System (INIS)

Nyambok, I.O.

1986-01-01

The problem associated with black cotton and lateritic soils because of the swelling-shrinkage property of their constituent clay minerals were investigated. Samples of black cotton lateritic soils were collected from different parts of Kenya. The samples were analysed for their mineral compositions and later treated with hydrated lime in order to eliminate the swelling shrinkage behaviour. The samples were subsequently tested for their engineering properties in a soil mechanics laboratory using shear box and Casagrande apparatus. It was found that the chemical treatment of the soils with hydrated lime removes their plastic property and improves their shear strength. (author)

Genesis and Development of Soils along Different Geomorphic Surfaces in Kouh Birk Area, Mehrestan City

Directory of Open Access Journals (Sweden)

Mohammad Akbar Bahoorzahi

2017-02-01

the presence of argillic and petrocalcic horizons in rock pediment, soils of this surface were more developed compared to other landforms. High amount of CaCO3 (39.5% was observed in pedon 4 on rock pediment geomorphic surface which is attributed to calcareous parent material. The presence of argillic horizon in this geomorphic position is due to the more available water of the past climate. The maximum salinity was observed in the mantled pediments. Calcic over gypsic horizons formed in pedon 7 on alluvial fan surface due to higher solubility of gypsum than calcium carbonate. Kaolinite, illite, chlorite, and palygorskite clay minerals were found in pedons 1 and 4 on rock pediment. Palygorskite in this position seems to be pedogenic, but kaolinite, illite, and chlorite are inherited from parent material. Mantled pediment and alluvial fan showed smectite, kaolinite, illite, chlorite, and palygorskite clay minerals. Pedogenic smectite in this position is probably formed from weathering of illite and chlorite. On the other hand, palygorskite stability decreased in mantled pediment surface. This is the reason why smectite was the dominant clay mineral in this landform. Clay and calcite coatings were investigated in Bt horizon of pedon 1 (rock pediment. Coatings and infillings of calcite in Bk2 horizon of the same geomorphic position caused a calcic crystallitic b fabric. A diffused clay coating due to the presence of Na in Btn horizon of pedon 3 in rock pediment was observed. Micromorphological observations of By2 horizon in pedon 5 (mantled pediment showed gypsum interlocked plates and gypsum infillings. Interlocked plates formed due to re-solubility of gypsum crystals. Micro spars and infillings of calcite are among dominant pedofeatures found in Bk1 horizon of pedon 7 (alluvial fan geomorphic surface. A calcic crystallitic b fabric and Primary calcite mineral were also observed in this pedon. Release of Ca from calcareous parent material caused Ca+2 to SO4-2 ratio to

Nitrous oxide emissions respond differently to mineral and organic nitrogen sources in contrasting soil types.

Science.gov (United States)

Pelster, David E; Chantigny, Martin H; Rochette, Philippe; Angers, Denis A; Rieux, Christine; Vanasse, Anne

2012-01-01

The use of various animal manures for nitrogen (N) fertilization is often viewed as a viable replacement for mineral N fertilizers. However, the impacts of amendment type on NO production may vary. In this study, NO emissions were measured for 2 yr on two soil types with contrasting texture and carbon (C) content under a cool, humid climate. Treatments consisted of a no-N control, calcium ammonium nitrate, poultry manure, liquid cattle manure, or liquid swine manure. The N sources were surface applied and immediately incorporated at 90 kg N ha before seeding of spring wheat ( L.). Cumulative NO-N emissions from the silty clay ranged from 2.2 to 8.3 kg ha yr and were slightly lower in the control than in the fertilized plots ( = 0.067). The 2-yr mean NO emission factors ranged from 2.0 to 4.4% of added N, with no difference among N sources. Emissions of NO from the sandy loam soil ranged from 0.3 to 2.2 kg NO-N ha yr, with higher emissions with organic than mineral N sources ( = 0.015) and the greatest emissions with poultry manure ( < 0.001). The NO emission factor from plots amended with poultry manure was 1.8%, more than double that of the other treatments (0.3-0.9%), likely because of its high C content. On the silty clay, the yield-based NO emissions (g NO-N kg grain yield N) were similar between treatments, whereas on the sandy loam, they were greatest when amended with poultry manure. Our findings suggest that, compared with mineral N sources, manure application only increases soil NO flux in soils with low C content. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Redistribution of soil nitrogen, carbon and organic matter by mechanical disturbance during whole-tree harvesting in northern hardwoods

Science.gov (United States)

Ryan, D.F.; Huntington, T.G.; Wayne, Martin C.

1992-01-01

To investigate whether mechanical mixing during harvesting could account for losses observed from forest floor, we measured surface disturbance on a 22 ha watershed that was whole-tree harvested. Surface soil on each 10 cm interval along 81, randomly placed transects was classified immediately after harvesting as mineral or organic, and as undisturbed, depressed, rutted, mounded, scarified, or scalped (forest floor scraped away). We quantitatively sampled these surface categories to collect soil in which preharvest forest floor might reside after harvest. Mechanically mixed mineral and organic soil horizons were readily identified. Buried forest floor under mixed mineral soil occurred in 57% of mounds with mineral surface soil. Harvesting disturbed 65% of the watershed surface and removed forest floor from 25% of the area. Mechanically mixed soil under ruts with organic or mineral surface soil, and mounds with mineral surface soil contained organic carbon and nitrogen pools significantly greater than undisturbed forest floor. Mechanical mixing into underlying mineral soil could account for the loss of forest floor observed between the preharvest condition and the second growing season after whole-tree harvesting. ?? 1992.

Mineralization of residual fertilizer nitrogen in soil after rice harvest

International Nuclear Information System (INIS)

Hazarika, S.; Sarkar, M.C.

1994-01-01

Remineralization of immobilized 15 N labelled urea N applied to rice crop at the rate of 180 kg N/ha was determined. Mineral N increased rapidly up to 14 days of incubation and thereafter remained more or less constant. The recovery of fertilizer as mineral N varied between 0.7 and 3.1 μg/g soil. The percent mineralization of labelled organic N ranged between 3.1 and 9.5. (author). 5 refs., 2 tabs., 1 fig

Nitrification and nitrogen mineralization in agricultural soils contaminated by copper mining activities in Central Chile

OpenAIRE

Moya, Héctor; Verdejo, José; Yáñez, Carolina; Álvaro, Juan E.; Sauvé, Sébastien; Neaman, Alexander

2017-01-01

Microbiological bioassays of nitrification and nitrogen mineralization have been used for evaluation of soil quality on metal-contaminated soils. We evaluated the effectiveness of nitrification and nitrogen mineralization bioassays as quality indicators of soil degradation caused by metal contamination. We performed standard tests based on protocols of ISO 14238 (2012) and ISO 15685 (2012) on 90 soil samples collected from agricultural areas in central Chile that were historically contaminate...

Formation and Stability of Microbially Derived Soil Organic Matter

Science.gov (United States)

Waldrop, M. P.; Creamer, C.; Foster, A. L.; Lawrence, C. R.; Mcfarland, J. W.; Schulz, M. S.

2017-12-01

Soil carbon is vital to soil health, food security, and climate change mitigation, but the underlying mechanisms controlling the stabilization and destabilization of soil carbon are still poorly understood. There has been a conceptual paradigm shift in how soil organic matter is formed which now emphasizes the importance of microbial activity to build stable (i.e. long-lived) and mineral-associated soil organic matter. In this conceptual model, the consumption of plant carbon by microorganisms, followed by subsequent turnover of microbial bodies closely associated with mineral particles, produces a layering of amino acid and lipid residues on the surfaces of soil minerals that remains protected from destabilization by mineral-association and aggregation processes. We tested this new model by examining how isotopically labeled plant and microbial C differ in their fundamental stabilization and destabilization processes on soil minerals through a soil profile. We used a combination of laboratory and field-based approaches to bridge multiple spatial scales, and used soil depth as well as synthetic minerals to create gradients of soil mineralogy. We used Raman microscopy as a tool to probe organic matter association with mineral surfaces, as it allows for the simultaneous quantification and identification of living microbes, carbon, minerals, and isotopes through time. As expected, we found that the type of minerals present had a strong influence on the amount of C retained, but the stabilization of new C critically depends on growth, death, and turnover of microbial cells. Additionally, the destabilization of microbial residue C on mineral surfaces was little affected by flushes of DOC relative to wet-dry cycles alone. We believe this new insight into microbial mechanisms of C stabilization in soils will eventually lead to new avenues for measuring and modeling SOM dynamics in soils, and aid in the management of soil C to mediate global challenges.

Effect of pH on the adsorption of carbendazim in Polish mineral soils

International Nuclear Information System (INIS)

Paszko, Tadeusz

2012-01-01

The study aimed to determine the influence of pH on the adsorption of carbendazim in soil profiles of three mineral agricultural soils: Hyperdystric Arenosol, Haplic Luvisol and Hypereutric Cambisol. In the examined pH range between 3 and 7 the adsorption of carbendazim was inversely correlated to the pH of the soil. The adsorption coefficients were in the range between 0.3 and 151.8 mL g −1 . Decreasing the pH in the soil suspensions from 7 to 3 increased the value of this coefficient by 3 to 70 times. A decrease in the amounts of organic matter down the soil profiles was not associated with weaker carbendazim adsorption. In the samples from all soil horizons, at pH values between 3 and 6, the predominant sorption process was carbendazim adsorption on clay minerals. The adsorption of carbendazim on organic matter prevailed over that on clays only at pH > 6 and only in the Ap horizon of the examined soils. The developed mathematical models yielded very good results when the adsorption of the protonated form of carbendazim was assumed to be the predominant adsorption process on clays together with the adsorption of neutral molecules on organic matter and clays. The results from both the model fitting and the experiments revealed the negative effect of Al oxides and hydroxides and Al cations on the adsorption of the protonated form of carbendazim on clay minerals. The developed models successfully described the pH-dependent adsorption processes of carbendazim for both data from particular soil horizons and those from all three examined soil profiles. -- Highlights: ► Adsorption of carbendazim in soils was inversely correlated to soil pH. ► At low pH carbendazim was adsorbed predominantly by clay minerals. ► Al 3+ influenced adsorption of the protonated form of carbendazim on clays. ► Created models predict pH-dependent sorption processes in the whole soil profiles.

Correlation studies of mineral nutrients' concentrations in soils and ...

African Journals Online (AJOL)

Ananas comosus) plants growth and development in the southern agricultural zone of Cross River State. Fields experiment were conducted to evaluate the relationships existing between mineral nqutrients in the soils and pineapple plants.

On the recovery of oil-polluted soils with mineral zeolite

International Nuclear Information System (INIS)

Rasulova, Z.Q.; Huseynzade, G.A.; Hajiyeva, S.A.

2014-01-01

Full text : The purpose of this study - ecological analysis of soil invertebrates in the oil-polluted soils and testing adsorbent for purificatication of such soils. In the study cenoses of Absheron 48 species of soil invertebrates belonging to 5 families, 13 orders, 24 families were revealed. For these purposes the local mineral -zeolite was applied. The results of experiments showed that refinement with zeolite makes positive impact on development of fauna of soil invertebrates. The studies were conducted in 2011-2013 in locally contaminated areas of oilfields of Absheron Peninsula. Radiation background in the studied areas ranges from 50-600 mR/hr

Impact of Poultry Litter Cake, Cleanout, and Bedding following Chemical Amendments on Soil C and N Mineralization

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Dexter B. Watts

2012-01-01

Full Text Available Poultry litter is a great alternative N source for crop production. However, recent poultry litter management changes, and increased chemical amendment use may impact its N availability. Thus, research was initiated to evaluate the effect that broiler cake and total cleanout litter amended with chemical additives have on C and N mineralization. A 35-day incubation study was carried out on a Hartsells fine sandy loam (fine-loamy, siliceous, subactive, thermic Typic Hapludults soil common to the USA Appalachian Plateau region. Three poultry litter components (broiler cake, total cleanout, and bedding material from a broiler house were evaluated and compared to a soil control. Chemical amendments lime (CaCO3, gypsum (CaSO4, aluminum sulfate (AlSO4, and ferrous sulfate (FeSO4 were added to the poultry litter components to determine their impact on C and N mineralization. Litter component additions increased soil C mineralization in the order of broiler cake > total cleanout > bedding > soil control. Although a greater concentration of organic C was observed in the bedding, broiler cake mineralized the most C, which can be attributed to differences in the C : N ratio between treatments. Chemical amendment in addition to the manured soil also impacted C mineralization, with AlSO4 generally decreasing mineralization. Nitrogen mineralization was also significantly affected by poultry litter component applications. Broiler cake addition increased N availability followed by total cleanout compared to soil control, while the bedding resulted in net N immobilization. Chemical amendments impacted N mineralization primarily in the broiler cake amended soil where all chemical amendments decreased mineralization compared to the no chemical amendment treatment. This short-term study (35-day incubation indicates that N availability to crops may be different depending on the poultry litter component used for fertilization and chemical amendment use which could

Characterization of Minerals: From the Classroom to Soils to Talc Deposits

Science.gov (United States)

McNamee, Brittani D.

2013-01-01

This dissertation addresses different methods and challenges surrounding characterizing and identifying minerals in three environments: in the classroom, in soils, and in talc deposits. A lab manual for a mineralogy and optical mineralogy course prepares students for mineral characterization and identification by giving them the methods and tools…

Dissolved organic carbon and nitrogen mineralization strongly affect co2 emissions following lime application to acidic soil

International Nuclear Information System (INIS)

Shaaban, M.; Peng, Q.; Lin, S.; Wu, Y.

2014-01-01

Emission of greenhouse gases from agricultural soils has main contribution to the climatic change and global warming. Dynamics of dissolved organic carbon (DOC) and nitrogen mineralization can affect CO/sub 2/ emission from soils. Influence of DOC and nitrogen mineralization on CO/sub 2/ emissions following lime application to acidic soil was investigated in current study. Laboratory experiment was conducted under aerobic conditions with 25% moisture contents (66% water-filled pore space) at 25 degree C in the dark conditions. Different treatments of lime were applied to acidic soil as follows: CK (control), L (low rate of lime: 0.2g lime / 100 g soil) and H (high rate of lime: 0.5g lime /100g soil). CO/sub 2/ emissions were measured by gas chromatography and dissolved organic carbon, NH4 +-N, NO/sub 3/ --N and soil pH were measured during incubation study. Addition of lime to acidic soil significantly increased the concentration of DOC and N mineralization rate. Higher concentrations of DOC and N mineralization, consequently, increased the CO/sub 2/ emissions from lime treated soils. Cumulative CO/sub 2/ emission was 75% and 71% higher from L and H treatments as compared to CK. The results of current study suggest that DOC and N mineralization are critical in controlling gaseous emissions of CO/sub 2/ from acidic soils following lime application. (author)

Sorptive and desorptive fractionation of dissolved organic matter by mineral soil matrices.

Science.gov (United States)

Oren, Adi; Chefetz, Benny

2012-01-01

Interactions of dissolved organic matter (DOM) with soil minerals, such as metal oxides and clays, involve various sorption mechanisms and may lead to sorptive fractionation of certain organic moieties. While sorption of DOM to soil minerals typically involves a degree of irreversibility, it is unclear which structural components of DOM correspond to the irreversibly bound fraction and which factors may be considered determinants. To assist in elucidating that, the current study aimed at investigating fractionation of DOM during sorption and desorption processes in soil. Batch DOM sorption and desorption experiments were conducted with organic matter poor, alkaline soils. Fourier-transform infrared (FTIR) and UV-Vis spectroscopy were used to analyze bulk DOM, sorbed DOM, and desorbed DOM fractions. Sorptive fractionation resulted mainly from the preferential uptake of aromatic, carboxylic, and phenolic moieties of DOM. Soil metal-oxide content positively affected DOM sorption and binding of some specific carboxylate and phenolate functional groups. Desorptive fractionation of DOM was expressed by the irreversible-binding nature of some carboxylic moieties, whereas other bound carboxylic moieties were readily desorbed. Inner-sphere, as opposed to outer-sphere, ligand-exchange complexation mechanisms may be responsible for these irreversible, as opposed to reversible, interactions, respectively. The interaction of aliphatic DOM constituents with soil, presumably through weak van der Waals forces, was minor and increased with increasing proportion of clay minerals in the soil. Revealing the nature of DOM-fractionation processes is of great importance to understanding carbon stabilization mechanisms in soils, as well as the overall fate of contaminants that might be associated with DOM. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

Results of mineral, chemical, and sulfate isotopic analyses of water, soil, rocks, and soil extracts from the Pariette Draw Watershed, Uinta Basin, Utah

Science.gov (United States)

Morrison, Jean M.; Tuttle, Michele L.W.; Fahy, Juli W.

2015-08-06

In 2010, Utah Department of Environmental Quality (DEQ) Division of Water Quality (UDWQ, 2010) determined that water quality in Pariette Draw was in violation of Federal and State water quality criteria for total dissolved solids (TDS), selenium (Se), and boron (B). The measure of total dissolved solids is the sum of all the major ion concentrations in solution and in this case, the dominant ions are sodium (Na) and sulfate (SO4), which can form salts like thenardite (Na2SO4) and mirabilite (Na2SO4⋅H2O). The Utah Department of Environmental Quality (2010) classified the contamination as natural background and from nonpoint sources related to regional lithology and irrigation practices. Although the daily loads of the constituents of concern and water chemistry have been characterized for parts of the watershed, little is known about the controls that bedrock and soil mineralogy have on salt, Se, and B storage and the water-rock interactions that influence the mobility of these components in ground and surface waters. Studies in the Uncompahgre River watershed in Colorado by Tuttle and others (2014a, 2014b) show that salt derived from weathering of shale in a semiarid climate is stored in a variety of minerals that contribute solutes to runoff and surface waters based on a complex set of conditions such as water availability, geomorphic position (for example, topography controls the depth of salt accumulation in soils), water-table fluctuations, redox conditions, mineral dissolution kinetics, ion-exchange reactions, and secondary mineral formation. Elements like Se and B commonly reside in soluble salt phases, so knowledge of the behavior of salt minerals also sheds light on the behavior of associated contaminants.

Uranyl adsorption at clay mineral surfaces

Energy Technology Data Exchange (ETDEWEB)

Roesch, N. [Technische Univ. Muenchen (Germany). Fachgebiet Theoretische Chemie

2016-11-01

This first systematic survey of actinide adsorption at complex clay mineral surfaces, which provided new insights at the atomic level, is currently being extended to neptunyl NpO{sub 2}{sup +} and more complex minerals, like iron-substituted phyllosilicates. In this way we examine if the concepts developed so far can be applied more generally to support the interpretation of pertinent experiments. A further facet of these studies is to account also for the dynamic nature of the mineral/water interface by means of exemplary dynamic simulations.

Zinc oxide nanoparticles affect carbon and nitrogen mineralization of Phoenix dactylifera leaf litter in a sandy soil.

Science.gov (United States)

Rashid, Muhammad Imtiaz; Shahzad, Tanvir; Shahid, Muhammad; Ismail, Iqbal M I; Shah, Ghulam Mustafa; Almeelbi, Talal

2017-02-15

We investigated the impact of zinc oxide nanoparticles (ZnO NPs; 1000mgkg -1 soil) on soil microbes and their associated soil functions such as date palm (Phoenix dactylifera) leaf litter (5gkg -1 soil) carbon and nitrogen mineralization in mesocosms containing sandy soil. Nanoparticles application in litter-amended soil significantly decreased the cultivable heterotrophic bacterial and fungal colony forming units (cfu) compared to only litter-amended soil. The decrease in cfu could be related to lower microbial biomass carbon in nanoparticles-litter amended soil. Likewise, ZnO NPs also reduced CO 2 emission by 10% in aforementioned treatment but this was higher than control (soil only). Labile Zn was only detected in the microbial biomass of nanoparticles-litter applied soil indicating that microorganisms consumed this element from freely available nutrients in the soil. In this treatment, dissolved organic carbon and mineral nitrogen were 25 and 34% lower respectively compared to litter-amended soil. Such toxic effects of nanoparticles on litter decomposition resulted in 130 and 122% lower carbon and nitrogen mineralization efficiency respectively. Hence, our results entail that ZnO NPs are toxic to soil microbes and affect their function i.e., carbon and nitrogen mineralization of applied litter thus confirming their toxicity to microbial associated soil functions. Copyright © 2016 Elsevier B.V. All rights reserved.

Influence of a soil enzyme on iron-cyanide complex speciation and mineral adsorption.

Science.gov (United States)

Zimmerman, Andrew R; Kang, Dong-Hee; Ahn, Mi-Youn; Hyun, Seunghun; Banks, M Katherine

2008-01-01

Cyanide is commonly found as ferrocyanide [Fe(II)(CN)(6)](-4) and in the more mobile form, ferricyanide [Fe(III)(CN)(6)](-3) in contaminated soils and sediments. Although soil minerals may influence ferrocyanide speciation, and thus mobility, the possible influence of soil enzymes has not been examined. In a series of experiments conducted under a range of soil-like conditions, laccase, a phenoloxidase enzyme derived from the fungi Trametes versicolor, was found to exert a large influence on iron-cyanide speciation and mobility. In the presence of laccase, up to 93% of ferrocyanide (36-362ppm) was oxidized to ferricyanide within 4h. No significant effect of pH (3.6 and 6.2) or initial ferrocyanide concentration on the extent or rate of oxidation was found and ferrocyanide oxidation did not occur in the absence of laccase. Relative to iron-cyanide-mineral systems without laccase, ferrocyanide adsorption to aluminum hydroxide and montmorillonite decreased in the presence of laccase and was similar to or somewhat greater than that of ferricyanide without laccase. Laccase-catalyzed conversion of ferrocyanide to ferricyanide was extensive though up to 33% of the enzyme was mineral-bound. These results demonstrate that soil enzymes can play a major role in ferrocyanide speciation and mobility. Biotic soil components must be considered as highly effective oxidation catalysts that may alter the mobility of metals and metal complexes in soil. Immobilized enzymes should also be considered for use in soil metal remediation efforts.

30 CFR 823.14 - Soil replacement.

Science.gov (United States)

2010-07-01

... 30 Mineral Resources 3 2010-07-01 2010-07-01 false Soil replacement. 823.14 Section 823.14 Mineral Resources OFFICE OF SURFACE MINING RECLAMATION AND ENFORCEMENT, DEPARTMENT OF THE INTERIOR PERMANENT PROGRAM PERFORMANCE STANDARDS SPECIAL PERMANENT PROGRAM PERFORMANCE STANDARDS-OPERATIONS ON PRIME FARMLAND § 823.14 Soil replacement. (a) Soil...

Decreasing soil water Ca2+ reduces DOC adsorption in mineral soils: implications for long-term DOC trends in an upland forested catchment in southern Ontario, Canada.

Science.gov (United States)

Kerr, Jason Grainger; Eimers, M Catherine

2012-06-15

Positive trends in dissolved organic carbon (DOC) concentration have been observed in surface waters throughout North America and northern Europe. Although adsorption in mineral soils is an important driver of DOC in upland streams, little is known about the potential for changes in DOC adsorption to contribute to these trends. We hypothesized that long-term declines in soil water Ca(2+) levels, in response to declining acid deposition, might influence DOC adsorption and that this could contribute to long-term DOC trends in an upland forested catchment in south-central Ontario, Canada. Between 1987 and 2009, DOC concentrations increased significantly (pDOC concentration (DOC(np)), which is a measure of the soil water DOC concentration at equilibrium with the soil, ranged from 1.27 to 3.75 mg L(-1) in B horizon soils. This was similar to the mean DOC concentrations of B horizon soil water (2.04-6.30 mg L(-1)) and stream water (2.20 mg L(-1)), indicating that soil and stream water DOC concentrations are controlled by equilibrium processes at the soil-water interface. Adsorption experiments using variable Ca(2+) concentrations demonstrated that as Ca(2+) decreased the DOC(np) increased (1.96 to 4.74 mg L(-1)), which was consistent with the observed negative correlation between DOC and Ca(2+) in B horizon soil water (pDOC adsorption (p>0.05), indicating that changes in DOC adsorption might be related to cation bridging. We conclude that declines in soil water Ca(2+) concentration can contribute to increasing DOC trends in upland streams by reducing DOC adsorption in mineral soils. Copyright © 2012 Elsevier B.V. All rights reserved.

Researches concerning the influence of inorganic substratum over glyphosate mineralization capacity in soil

Directory of Open Access Journals (Sweden)

Monica NEGREA

2009-05-01

Full Text Available The object of this work was to study the dynamic of glyphosate mineralization in different agricultural soils characteristic to the west part of Romania: Black Chernozem, Typical Gleysol, Phaeozom and Slight Vertisol with moderate carbonatation. The degradation experiment was conducted under controlled laboratory conditions using Glyphosatephosphonomethyl- 14C-labeled with specific activity 2,2mCi/mmol. The experimental results indicated that the dynamic of glyphosate mineralization until the stage CO2 in present of inorganic compounds is different for each soil, the mineralization of the herbicide is important in the first days of incubation and then decreases with time until the end of experimentation.

Spectroscopic Evidence of the Improvement of Reactive Iron Mineral Content in Red Soil by Long-Term Application of Swine Manure.

Directory of Open Access Journals (Sweden)

Chichao Huang

Full Text Available Mineral elements in soil solutions are thought to be the precursor of the formation of reactive minerals, which play an important role in global carbon (C cycling. However, information regarding the regulation of mineral elements release in soil is scarce. Here, we examined the long-term (i.e., 23 yrs effects of fertilisation practices on Fe minerals in a red soil in Southern China. The results from chemical analysis and Fourier-transform infrared spectroscopy showed that long-term swine manure (M treatment released greater amounts of minerals into soil solutions than chemical fertilisers (NPK treatment, and Fe played a dominant role in the preservation of dissolved organic C. Furthermore, Fe K-edge X-ray absorption near-edge fine structure spectroscopy demonstrated that reactive Fe minerals were mainly composed of less crystalline ferrihydrite in the M-treated soil and more crystalline goethite in the NPK-treated soil. In conclusion, this study reported spectroscopic evidence of the improvement of reactive Femineral content in the M-treated soil colloids when compared to NPK-treated soil colloids.

The Bio-accessibility of Synthetic Fe-Organo Complexes in Subsurface Soil with Elevated Temperature: a Proxy for the Vulnerability of Mineral Associated Carbon to Warming Rachel C. Porras, Peter S. Nico, and Margaret Torn Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA

Science.gov (United States)

Porras, R. C.; Hicks Pries, C.

2015-12-01

Globally, subsurface soils (>30 cm) represent an important reservoir of soil organic carbon (SOC). However, the vulnerability of this deep SOC and, in particular mineral-associated SOC, to warming, and its potential to amplify the effects of climate change is highly uncertain. To gain insight into the bio-accessibility and temperature sensitivity of mineral-associated organic C, we conducted a series of incubations using soils collected from three depths (0-10, 50-60, and 80-90 cm) under coniferous forest. The soils are moderately acidic (mean pH=6.5) sandy, mixed, mesic Ultic Haploxeralfs. To understand how mechanisms controlling SOC bio-accessibilty or temperature sensitivity differ with depth and with the properties of Fe-organo complexes (i.e.,degree of crystallinity, amount of reactive surface area, or surface saturation), we used a 13C labeled glucose substrate to prepare synthetic Fe-organo complexes spanning a range of crystallinity and mineral surface saturation. The synthetic Fe-organo complexes were then added to soil from three depths. The soils containing the 13C labeled Fe-organo adduct were incubated at two temperatures (ambient and +4°C) and respired 13CO2 was measured and used to estimate flux rates. Differences in measured 13CO2 fluxes as a function of depth, surface loading, and mineral properties are discussed in terms of their implications for the temperature sensitivity of mineral protected organic carbon in subsurface soils.

Carbon dioxide emissions from semi-arid soils amended with biochar alone or combined with mineral and organic fertilizers.

Science.gov (United States)

Fernández, José M; Nieto, M Aurora; López-de-Sá, Esther G; Gascó, Gabriel; Méndez, Ana; Plaza, César

2014-06-01

Semi-arid soils cover a significant area of Earth's land surface and typically contain large amounts of inorganic C. Determining the effects of biochar additions on CO2 emissions from semi-arid soils is therefore essential for evaluating the potential of biochar as a climate change mitigation strategy. Here, we measured the CO2 that evolved from semi-arid calcareous soils amended with biochar at rates of 0 and 20tha(-1) in a full factorial combination with three different fertilizers (mineral fertilizer, municipal solid waste compost, and sewage sludge) applied at four rates (equivalent to 0, 75, 150, and 225kg potentially available Nha(-1)) during 182 days of aerobic incubation. A double exponential model, which describes cumulative CO2 emissions from two active soil C compartments with different turnover rates (one relatively stable and the other more labile), was found to fit very well all the experimental datasets. In general, the organic fertilizers increased the size and decomposition rate of the stable and labile soil C pools. In contrast, biochar addition had no effects on any of the double exponential model parameters and did not interact with the effects ascribed to the type and rate of fertilizer. After 182 days of incubation, soil organic and microbial biomass C contents tended to increase with increasing the application rates of organic fertilizer, especially of compost, whereas increasing the rate of mineral fertilizer tended to suppress microbial biomass. Biochar was found to increase both organic and inorganic C contents in soil and not to interact with the effects of type and rate of fertilizer on C fractions. As a whole, our results suggest that the use of biochar as enhancer of semi-arid soils, either alone or combined with mineral and organic fertilizers, is unlikely to increase abiotic and biotic soil CO2 emissions. Copyright © 2014 Elsevier B.V. All rights reserved.

Study of Adsorption of Phenanthrene on Different Types of Clay Minerals

International Nuclear Information System (INIS)

Contreras, M. L.; Escolano, O.; Rodriguez, V.; Diaz, F. J.; Perez, R.; Garcia, S.; Garcia Frutos, F. J.

2003-01-01

The fate and behaviour of non-ionic hydrophobic organic compounds in deep soil is mainly controlled by the mineral fraction present in the soil due to the very low organic carbon content of the deep soil. The mineral fraction that may greatly influence the fate and transport of these compounds due to its presence and properties are the clay minerals. Clay minerals also become increasingly important in low organic matter content soils. There tree, studies of non-ionic hydrophobic organic compounds adsorption on clay minerals without organic matter are necessary lo better understand the fate and transport of these compounds. In this work we used phenanthrene as model compound of non-ionic hydrophobic organic compound and four pure clay minerals: kaolinite, illite, montmorillonite, and vermiculite including muscovite mica. These clays minerals are selected due to its abundance in represents ve Spanish soils and different properties as its structural layers and expanding capacity. Batch experiments were performed using phenanthrene aqueous solutions and the clays selected. Phenanthrene sorption isotherms for all clays, except muscovite mica, were best described by the Freundlich model. Physical sorption on the external surfaces is the most probable adsorption mechanisms. In this sense, the presence of non-polar nano-sites on clay surfaces could determine the adsorption of phenanthrene by hydrophobic interaction on these sites. (Author) 22 refs

Oxygen isotope fractionation effects in soil water via interaction with cations (Mg, Ca, K, Na) adsorbed to phyllosilicate clay minerals

Science.gov (United States)

Oerter, Erik; Finstad, Kari; Schaefer, Justin; Goldsmith, Gregory R.; Dawson, Todd; Amundson, Ronald

2014-07-01

In isotope-enabled hydrology, soil and vadose zone sediments have been generally considered to be isotopically inert with respect to the water they host. This is inconsistent with knowledge that clay particles possessing an electronegative surface charge and resulting cation exchange capacity (CEC) interact with a wide range of solutes which, in the absence of clays, have been shown to exhibit δ18O isotope effects that vary in relation to the ionic strength of the solutions. To investigate the isotope effects caused by high CEC clays in mineral-water systems, we created a series of monominerallic-water mixtures at gravimetric water contents ranging from 5% to 32%, consisting of pure deionized water of known isotopic composition with homoionic (Mg, Ca, Na, K) montmorillonite. Similar mixtures were also created with quartz to determine the isotope effect of non-, or very minimally-, charged mineral surfaces. The δ18O value of the water in these monominerallic soil analogs was then measured by isotope ratio mass spectrometry (IRMS) after direct headspace CO2 equilibration. Mg- and Ca-exchanged homoionic montmorillonite depleted measured δ18O values up to 1.55‰ relative to pure water at 5% water content, declining to 0.49‰ depletion at 30% water content. K-montmorillonite enriched measured δ18O values up to 0.86‰ at 5% water content, declining to 0.11‰ enrichment at 30% water. Na-montmorillonite produces no measureable isotope effect. The isotope effects observed in these experiments may be present in natural, high-clay soils and sediments. These findings have relevance to the interpretation of results of direct CO2-water equilibration approaches to the measurement of the δ18O value of soil water. The adsorbed cation isotope effect may bear consideration in studies of pedogenic carbonate, plant-soil water use and soil-atmosphere interaction. Finally, the observed isotope effects may prove useful as molecular scale probes of the nature of mineral

Accelerated decay rates drive soil organic matter persistence and storage in temperate forests via greater mineral stabilization of microbial residues.

Science.gov (United States)

Phillips, R.; Craig, M.; Turner, B. L.; Liang, C.

2017-12-01

, our results indicate that tree species influence soil C and N storage owing to how differences in decay rates affect mineral stabilization of organic matter. Further, our findings indicate that slow decay promotes soil C and N stocks at the soil surface, whereas fast decay promotes greater soil C and N stocks at depth.

Sorption Energy Maps of Clay Mineral Surfaces

International Nuclear Information System (INIS)

Cygan, Randall T.; Kirkpatrick, R. James

1999-01-01

A molecular-level understanding of mineral-water interactions is critical for the evaluation and prediction of the sorption properties of clay minerals that may be used in various chemical and radioactive waste disposal methods. Molecular models of metal sorption incorporate empirical energy force fields, based on molecular orbital calculations and spectroscopic data, that account for Coulombic, van der Waals attractive, and short-range repulsive energies. The summation of the non-bonded energy terms at equally-spaced grid points surrounding a mineral substrate provides a three dimensional potential energy grid. The energy map can be used to determine the optimal sorption sites of metal ions on the exposed surfaces of the mineral. By using this approach, we have evaluated the crystallographic and compositional control of metal sorption on the surfaces of kaolinite and illite. Estimates of the relative sorption energy and most stable sorption sites are derived based on a rigid ion approximation

Priming effects of the endophytic fungus Phomopsis liquidambari on soil mineral N transformations.

Science.gov (United States)

Chen, Yan; Ren, Cheng-Gang; Yang, Bo; Peng, Yao; Dai, Chuan-Chao

2013-01-01

Nitrogen (N) is a crucial nutrient for soil biota, and its cycling is determined by the organic carbon decomposing process. Some endophytic fungi are latent saprotrophs that trigger their saprotrophic metabolism to promote litter organic matter cycling as soon as the host tissue senesces or dies. However, the effects of endophytic fungi on litter and soil N dynamics in vitro have rarely been investigated. In this study, we investigated N dynamics (total and mineral N) in both litter and soil in incubations of a pure culture of an endophytic fungus Phomopsis liquidambari with litter and following soil burial of the litter. Soil enzymes and microbial communities participating in the N transformations were also investigated. A pure culture of P. liquidambari released litter NH (4) (+) -N in the initial stages (10 days) of the incubation. However, following soil burial, the presence of both P. liquidambari and soil ammonia-oxidizing bacteria (AOB) resulted in an increase in soil NO (3) (-) -N. These results indicate that the endophytic fungus P. liquidambari in vitro stimulates organic mineralization and promote NH (4) (+) -N release. Such effects triggered soil AOB-driven nitrification process.

Probing the rhizosphere to define mineral organic relationships

Science.gov (United States)

Schulz, M. S.; Dohnalkova, A.; Stonestrom, D. A.

2016-12-01

Soil organic matter (SOM) accumulation and stabilization over time is an important process as soils are a large carbon reservoir in which feedbacks under changing climates are unclear. The association of SOM with poorly crystalline or short-range-ordered secondary minerals has been shown to be important for carbon stabilization. Commonly used soil extraction techniques display correlations of SOM with secondary phases but do not show causation. The fate of root exudates in soils and processes controlling exudate associations with mineral phases are as yet structurally undefined. Sub-micron exploration of in-situ relations provides valuable information on SOM-mineral interactions. Soils of the Santa Cruz (California) marine terrace chronosequence are used to illustrate changes in deep (> 1 m) rhizosphere through time. Cracks and soil ped faces are sites of high root density and organic matter (biofilm or mucilage) deposition. We employ a variety of scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM) techniques for high resolution imaging and elemental analyses of deep rhizosphere and associated carbon mineral interactions. In these coastal prairie soils microscopy reveals secondary clay minerals associated with and possibly forming from organic-rich mucilage that occurs along the aforementioned rooting networks on fracture surfaces. We hypothesize that the production of secondary clays in the rhizosphere is an important mode of C incorporation into secondary minerals.

Spatial variability of isoproturon mineralizing activity within an agricultural field: Geostatistical analysis of simple physicochemical and microbiological soil parameters

Energy Technology Data Exchange (ETDEWEB)

El Sebai, T. [UMR Microbiologie et Geochimie des Sols, INRA/CMSE, 17 Rue Sully, BP 86510, 21065 Dijon Cedex (France); Lagacherie, B. [UMR Microbiologie et Geochimie des Sols, INRA/CMSE, 17 Rue Sully, BP 86510, 21065 Dijon Cedex (France); Soulas, G. [UMR Microbiologie et Geochimie des Sols, INRA/CMSE, 17 Rue Sully, BP 86510, 21065 Dijon Cedex (France); Martin-Laurent, F. [UMR Microbiologie et Geochimie des Sols, INRA/CMSE, 17 Rue Sully, BP 86510, 21065 Dijon Cedex (France)]. E-mail: fmartin@dijon.inra.fr

2007-02-15

We assessed the spatial variability of isoproturon mineralization in relation to that of physicochemical and biological parameters in fifty soil samples regularly collected along a sampling grid delimited across a 0.36 ha field plot (40 x 90 m). Only faint relationships were observed between isoproturon mineralization and the soil pH, microbial C biomass, and organic nitrogen. Considerable spatial variability was observed for six of the nine parameters tested (isoproturon mineralization rates, organic nitrogen, genetic structure of the microbial communities, soil pH, microbial biomass and equivalent humidity). The map of isoproturon mineralization rates distribution was similar to that of soil pH, microbial biomass, and organic nitrogen but different from those of structure of the microbial communities and equivalent humidity. Geostatistics revealed that the spatial heterogeneity in the rate of degradation of isoproturon corresponded to that of soil pH and microbial biomass. - In field spatial variation of isoproturon mineralization mainly results from the spatial heterogeneity of soil pH and microbial C biomass.

Spatial variability of isoproturon mineralizing activity within an agricultural field: Geostatistical analysis of simple physicochemical and microbiological soil parameters

International Nuclear Information System (INIS)

El Sebai, T.; Lagacherie, B.; Soulas, G.; Martin-Laurent, F.

2007-01-01

We assessed the spatial variability of isoproturon mineralization in relation to that of physicochemical and biological parameters in fifty soil samples regularly collected along a sampling grid delimited across a 0.36 ha field plot (40 x 90 m). Only faint relationships were observed between isoproturon mineralization and the soil pH, microbial C biomass, and organic nitrogen. Considerable spatial variability was observed for six of the nine parameters tested (isoproturon mineralization rates, organic nitrogen, genetic structure of the microbial communities, soil pH, microbial biomass and equivalent humidity). The map of isoproturon mineralization rates distribution was similar to that of soil pH, microbial biomass, and organic nitrogen but different from those of structure of the microbial communities and equivalent humidity. Geostatistics revealed that the spatial heterogeneity in the rate of degradation of isoproturon corresponded to that of soil pH and microbial biomass. - In field spatial variation of isoproturon mineralization mainly results from the spatial heterogeneity of soil pH and microbial C biomass

Carbon storage and nutrient mobilization from soil minerals by deep roots and rhizospheres

DEFF Research Database (Denmark)

Callesen, Ingeborg; Harrison, Robert; Stupak, Inge

2016-01-01

studies on potential release of nutrients due to chemical weathering indicate the importance of root access to deep soil layers. Nutrient release profiles clearly indicate depletion in the top layers and a much higher potential in B and C horizons. Reviewing potential sustainability of nutrient supplies......Roots mobilize nutrients via deep soil penetration and rhizosphere processes inducing weathering of primary minerals. These processes contribute to C transfer to soils and to tree nutrition. Assessments of these characteristics and processes of root systems are important for understanding long......-term supplies of nutrient elements essential for forest growth and resilience. Research and techniques have significantly advanced since Olof Tamm’s 1934 “base mineral index” for Swedish forest soils, and the basic nutrient budget estimates for whole-tree harvesting systems of the 1970s. Recent research...

Liquid infused porous surfaces for mineral fouling mitigation.

Science.gov (United States)

Charpentier, Thibaut V J; Neville, Anne; Baudin, Sophie; Smith, Margaret J; Euvrard, Myriam; Bell, Ashley; Wang, Chun; Barker, Richard

2015-04-15

Prevention of mineral fouling, known as scale, is a long-standing problem in a wide variety of industrial applications, such as oil production, water treatment, and many others. The build-up of inorganic scale such as calcium carbonate on surfaces and facilities is undesirable as it can result in safety risks and associated flow assurance issues. To date the overwhelming amount of research has mainly focused on chemical inhibition of scale bulk precipitation and little attention has been paid to deposition onto surfaces. The development of novel more environmentally-friendly strategies to control mineral fouling will most probably necessitate a multifunctional approach including surface engineering. In this study, we demonstrate that liquid infused porous surfaces provide an appealing strategy for surface modification to reduce mineral scale deposition. Microporous polypyrrole (PPy) coatings were fabricated onto stainless steel substrates by electrodeposition in potentiostatic mode. Subsequent infusion of low surface energy lubricants (fluorinated oil Fluorinert FC-70 and ionic liquid 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMIm)) into the porous coatings results in liquid-repellent slippery surfaces. To assess their ability to reduce surface scaling the coatings were subjected to a calcium carbonate scaling environment and the scale on the surface was quantified using Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES). PPy surfaces infused with BMIm (and Fluorinert to a lesser extent) exhibit remarkable antifouling properties with the calcium carbonate deposition reduced by 18 times in comparison to untreated stainless steel. These scaling tests suggest a correlation between the stability of the liquid infused surfaces in artificial brines and fouling reduction efficiency. The current work shows the great potential of such novel coatings for the management of mineral scale fouling. Copyright © 2014 Elsevier Inc. All rights

Effects of sawdust and organo mineral fertilizer and their residual effect on the yield of maize on degrades soil

International Nuclear Information System (INIS)

Dania, S.O.; Fagbola, O.; Isitekhale, H.H.E.

2012-01-01

Conventional mineral fertilizer alone cannot sustain arable crop production in soil which top layer has been eroded hence it is necessary to employ the application of organic base fertilizer. A greenhouse experiment was conducted to investigate the effects of sawdust, organo mineral fertilizer and their residual effects on the growth and yield of maize. Organo mineral fertilizer is the combination of organic manure and mineral fertilizer. Simulated degraded soil was used and the experimental design was a 2 x 2 x 3 factorial in a completely randomized design with three replicates. The factors investigated were: two levels of organo mineral fertilizer (with and without), two levels of soil amendment (with and without sawdust) and three levels of application methods. The methods of organo mineral fertilizer used were ring, subsurface and mixed methods. The amendment of soil to sawdust was ratio 1:1 by volume. The growth and yield of maize was significantly (p = 0.05) higher in non-amended soil with OMF under different application methods compared to soil amended with sawdust with or without OMF application. Ring method of application of OMF in non-amended soil significantly increased the growth and yield of maize compared to other methods of OMF application. The residual effect of OMF and sawdust on the growth and yield of maize was significantly higher in non-amended soil with OMF under different application methods compared to soil amended with sawdust. Addition of sawdust to soil does not improve the growth and yield of maize with or without OMF and under different application methods. Organo mineral fertilizer using ring and subsurface application methods has a beneficial effect in improving the growth and yield of maize in degraded soil where the top layer has been eroded. (author)

Effects of sawdust and organo mineral fertilizer and their residual effect on the yield of maize on degraded soil

International Nuclear Information System (INIS)

Dania, S.O.; Fagbola, O.

2012-01-01

Conventional mineral fertilizer alone cannot sustain arable crop production in soil which top layer has been eroded hence it is necessary to employ the application of organic base fertilizer. A greenhouse experiment was conducted to investigate the effects of sawdust, organo mineral fertilizer and their residual effects on the growth and yield of maize. Organo mineral fertilizer is the combination of organic manure and mineral fertilizer. Simulated degraded soil was used and the experimental design was a 2 x 2 x 3 factorial in a completely randomized design with three replicates. The factors investigated were: two levels of organo mineral fertilizer (with and without), two levels of soil amendment (with and without sawdust) and three levels of application methods. The methods of organo mineral fertilizer used were ring, subsurface and mixed methods. The amendment of soil to sawdust was ratio 1: 1 by volume. The growth and yield of maize was significantly (p = 0.05) higher in non-amended soil with OMF under different application methods compared to soil amended with sawdust with or without OMF application. Ring method of application of OMF in non-amended soil significantly increased the growth and yield of maize compared to other methods of OMF application. The residual effect of OMF and sawdust on the growth and yield of maize was significantly higher in non-amended soil with OMF under different application methods compared to soil amended with sawdust. Addition of sawdust to soil does not improve the growth and yield of maize with or without OMF and under different application methods. Organo mineral fertilizer using ring and subsurface application methods has a beneficial effect in improving the growth and yield of maize in degraded soil where the top layer has been eroded. (author)

Mineralization of carbon and nitrogen from fresh and anaerobically stored sheep manure in soils of different texture

DEFF Research Database (Denmark)

Sørensen, P.; Jensen, E.S.

1995-01-01

A sandy loam soil was mixed with three different amounts of quartz sand and incubated with ((NH4)-N-15)(2)SO4 (60 mu g N g(-1) soil) and fresh or anaerobically stored sheep manure (60 mu g g(-1) soil). The mineralization-immobilization of N and the mineralization of C were studied during 84 days...

Factors for Microbial Carbon Sources in Organic and Mineral Soils from Eastern United States Deciduous Forests

Energy Technology Data Exchange (ETDEWEB)

Stitt, Caroline R. [Mills College, Oakland, CA (United States)

2013-09-16

Forest soils represent a large portion of global terrestrial carbon; however, which soil carbon sources are used by soil microbes and respired as carbon dioxide (CO2) is not well known. This study will focus on characterizing microbial carbon sources from organic and mineral soils from four eastern United States deciduous forests using a unique radiocarbon (14C) tracer. Results from the dark incubation of organic and mineral soils are heavily influenced by site characteristics when incubated at optimal microbial activity temperature. Sites with considerable differences in temperature, texture, and location differ in carbon source attribution, indicating that site characteristics play a role in soil respiration.

Bioremediation of experimental petroleum spills on mineral soils in the Vestfold Hills, Antarctica

International Nuclear Information System (INIS)

Kerry, E.

1993-01-01

The effect of nutrient and water enhancement on the biodegradation of petroleum was tested in Antarctic mineral soils. Nitrogen, phosphorus and potassium were applied in solution, with or without gum xanthan or plastic covers, to sites artificially contaminated with distillate. The effectiveness of these procedures was assessed by measuring changes in total petroleum hydrocarbons; heptadecane/pristane and octadecane/phytane ratios; in concentrations of major hydrocarbon components and in microbial numbers and activity. Significantly lower hydrocarbon concentration were recorded after one year in soils treated with fertilizer solutions, but only in the surface 3 cm. These soils also showed lowered heptadecane/pristane and octadecane/phytane ratios and had the highest levels of microbial activity relative to other plots. Soils treated with gum xanthan or covered with plastic had the highest residual hydrocarbon levels. Both treatments inhibited evaporative loss of hydrocarbon, and there were indications that gum xanthan was utilized by the microbiota as an alternative carbon source to distillate. Higher temperatures were recorded under the plastic but no stimulation of biodegradation was detected. Estimated numbers of metabolically active bacteria were in the range 10 7 to 10 8 g -1 dry weight of soil, with an estimated biomass of 0.03 to 0.26 mg g -1 soil. Estimated numbers of amoebae were in the range 10 6 10 7 g -1 soil (biomass of 2 to 4 mg g -1 ). The highest populations were recorded in fertilized, contaminated soils, the only soils where petroleum degradation was demonstrated. 23 refs., 1 fig., 4 tabs

Mineral capacity of peat soils organic matter and entry of Cs137 into perennial grasses

International Nuclear Information System (INIS)

Tsybulko, N.N.; Shapsheeva, T.P.; Arastovich, T.V.; Zajtsev, A.A.

2010-01-01

The results of the study of peat soils organic substance structure with various peat ash content are given. Contents of active organic substance and carbon of microbial biomass in peat and boggy soil with 20% peat ash content is 3.0-3.5 and 1.6-1.8 times higher correspondingly, than thus in peaty-gley soil with 70% peat ash content. At peat and boggy soil with low peat ash content Cs137 transition into hay is minimal. 14 times higher than at peaty-gley soil with 70% peat ash content. Application of fertilizers at peat and boggy soil reduces Cs137 transition factor 4.7-6.4 times if compared to peaty-gley soil (2.1-4.7 times). Close positive interconnection between Cs137 transition factors from soil into the plants and organic carbon soil contents, absolute contents of potentially mineralized carbon and mineralization degree

Soil mineral concentrations and soil microbial activity in grapevine inoculated with arbuscular mycorrhizal (AM fungus in Chile

Directory of Open Access Journals (Sweden)

Eduardo von Bennewitz

2008-01-01

Full Text Available A two year-experiment was carried out to study an effect of root inoculation with arbuscular mycorrhizal (AM fungus on soil mineral concentrations and soil microbial activity in grapevine (Vitis vi­ni­fe­ra cv. “Cabernet Sauvignon” cultivated in Chile. Plants were inoculated with a commercial granular inoculant (Mycosym Tri-ton® and cultivated in 20 L plastic pots filled with an unsterilized sandy clay soil from the Vertisols class under climatic conditions of Curicó (34°58´ S; 71°14´ W; 228 m ASL, Chile.Soil analyses were carried out at the beginning of the study and after two years (four samples of rhizospheric soil for each treatment to assess the effects of mycorrhizal infection on soil mineral concentration and physical properties. Soil microbial activity was measured by quantifying the soil production of CO2 in ten replications of 50 g of soil from each treatment. Root mycorrhizal infection was assessed through samples of fresh roots collected during 2005 and 2006. Fifty samples for each treatment were analyzed and the percentage of root length containing arbuscules and vesicles was assessed.During both years (2005 and 2006 all treatments showed mycorrhizal infection, even the Control treatment where no AM was applied. Mycorrhizal colonization did not affect the soil concentrations of N, P, K, Ca, Mg, K, Ca, Mg, Mn, Zn, Cu, Fe, B, organic matter, pH/KCl and ECe. Soil CO2-C in vitro production markedly decreased during the period of the study. No significant differences where detected among treatments in most cases.

[Nitrogen Fraction Distributions and Impacts on Soil Nitrogen Mineralization in Different Vegetation Restorations of Karst Rocky Desertification].

Science.gov (United States)

Hu, Ning; Ma, Zhi-min; Lan, Jia-cheng; Wu, Yu-chun; Chen, Gao-qi; Fu, Wa-li; Wen, Zhi-lin; Wang, Wen-jing

2015-09-01

In order to illuminate the impact on soil nitrogen accumulation and supply in karst rocky desertification area, the distribution characteristics of soil nitrogen pool for each class of soil aggregates and the relationship between aggregates nitrogen pool and soil nitrogen mineralization were analyzed in this study. The results showed that the content of total nitrogen, light fraction nitrogen, available nitrogen and mineral nitrogen in soil aggregates had an increasing tendency along with the descending of aggregate-size, and the highest content was occurred in 5mm and 2-5 mm classes, and the others were the smallest. With the positive vegetation succession, the weight percentage of > 5 mm aggregate-size classes was improved and the nitrogen storage of macro-aggregates also was increased. Accordingly, the capacity of soil supply mineral nitrogen and storage organic nitrogen were intensified.

Mineralization of alanine enantiomers in soil treated with heavy metals and nutrients

Directory of Open Access Journals (Sweden)

Pavel Formánek

2011-01-01

Full Text Available This work deals with the determination of the effect of heavy metals and nutrients applied to the soil on alanine enatiomers mineralization with the main focus on evaluating the effect on L/D alanine respiration rate ratio. This study was initiated because previous research works revealed a change in L/D amino acid respiration under acid- or heavy metal-stress in soil. Generally, D-amino acids artificially supplied to soil are less utilized by microorganisms compared with their L-enantiomers. Stress of soil microorganisms cause decreased discrimination of D-amino acids utilization. Also, previous research showed that an application of fertilizers or combinations of fertilizers may affect the mineralization rate of L-amino acids differently, compared with their D-enantiomers. The results of this study show, that the effect of both heavy metals and nutrients on the L/D ratio was not clear, increasing or decreasing this ratio. Further research is necessary to broaden this study.

Particle morphology and mineral structure of heavy metal-contaminated kaolin soil before and after electrokinetic remediation.

Science.gov (United States)

Roach, Nicole; Reddy, Krishna R; Al-Hamdan, Ashraf Z

2009-06-15

This study aims to characterize the physical distribution of heavy metals in kaolin soil and the chemical and structural changes in kaolinite minerals that result from electrokinetic remediation. Three bench-scale electrokinetic experiments were conducted on kaolin that was spiked with Cr(VI) alone, Ni (II) alone, and a combination of Cr(VI), Ni(II) and Cd(II) under a constant electric potential of 1VDC/cm for a total duration of 4 days. Transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD) analyses were performed on the soil samples before and after electrokinetic remediation. Results showed that the heavy metal contaminant distribution in the soil samples was not observable using TEM and EDX. EDX detected nickel and chromium on some kaolinite particles and titanium-rich, high-contrast particles, but no separate phases containing the metal contaminants were detected. Small amounts of heavy metal contaminants that were detected by EDX in the absence of a visible phase suggest that ions are adsorbed to kaolinite particle surfaces as a thin coating. There was also no clear correlation between semiquantitative analysis of EDX spectra and measured total metal concentrations, which may be attributed to low heavy metal concentrations and small size of samples used. X-ray diffraction analyses were aimed to detect any structural changes in kaolinite minerals resulting from EK. The diffraction patterns showed a decrease in peak height with decreasing soil pH value, which indicates possible dissolution of kaolinite minerals during electrokinetic remediation. Overall this study showed that the changes in particle morphology were found to be insignificant, but a relationship was found between the crystallinity of kaolin and the pH changes induced by the applied electric potential.

Particle morphology and mineral structure of heavy metal-contaminated kaolin soil before and after electrokinetic remediation

International Nuclear Information System (INIS)

Roach, Nicole; Reddy, Krishna R.; Al-Hamdan, Ashraf Z.

2009-01-01

This study aims to characterize the physical distribution of heavy metals in kaolin soil and the chemical and structural changes in kaolinite minerals that result from electrokinetic remediation. Three bench-scale electrokinetic experiments were conducted on kaolin that was spiked with Cr(VI) alone, Ni (II) alone, and a combination of Cr(VI), Ni(II) and Cd(II) under a constant electric potential of 1 VDC/cm for a total duration of 4 days. Transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD) analyses were performed on the soil samples before and after electrokinetic remediation. Results showed that the heavy metal contaminant distribution in the soil samples was not observable using TEM and EDX. EDX detected nickel and chromium on some kaolinite particles and titanium-rich, high-contrast particles, but no separate phases containing the metal contaminants were detected. Small amounts of heavy metal contaminants that were detected by EDX in the absence of a visible phase suggest that ions are adsorbed to kaolinite particle surfaces as a thin coating. There was also no clear correlation between semiquantitative analysis of EDX spectra and measured total metal concentrations, which may be attributed to low heavy metal concentrations and small size of samples used. X-ray diffraction analyses were aimed to detect any structural changes in kaolinite minerals resulting from EK. The diffraction patterns showed a decrease in peak height with decreasing soil pH value, which indicates possible dissolution of kaolinite minerals during electrokinetic remediation. Overall this study showed that the changes in particle morphology were found to be insignificant, but a relationship was found between the crystallinity of kaolin and the pH changes induced by the applied electric potential.

Amino acid and N mineralization dynamics in heathland soil after long-term warming and repetitive drought

NARCIS (Netherlands)

Andresen, L.C.; Bode, S.; Tietema, A.; Boeckx, P.; Rütting, T.

2015-01-01

Monomeric organic nitrogen (N) compounds such as free amino acids (FAAs) are an important resource for both plants and soil microorganisms and a source of ammonium (NH4+) via microbial FAA mineralization. We compared gross FAA dynamics with gross N mineralization in a Dutch heathland soil using a

Effect of three typical sulfide mineral flotation collectors on soil microbial activity.

Science.gov (United States)

Guo, Zunwei; Yao, Jun; Wang, Fei; Yuan, Zhimin; Bararunyeretse, P; Zhao, Yue

2016-04-01

The sulfide mineral flotation collectors are wildly used in China, whereas their toxic effect on soil microbial activity remains largely unexplored. In this study, isothermal microcalorimetric technique and soil enzyme assay techniques were employed to investigate the toxic effect of typical sulfide mineral flotation collectors on soil microbial activity. Soil samples were treated with different concentrations (0-100 μg•g - 1 soil) of butyl xanthate, butyl dithiophosphate, and sodium diethyldithiocarbamate. Results showed a significant adverse effect of butyl xanthate (p flotation collectors concentration from 20.0 to 100.0 μg•g(-1). However, the adverse effects of these three floatation collectors showed significant difference. The IC 20 of the investigated flotation reagents followed such an order: IC 20 (butyl xanthate) > IC 20 (sodium diethyldithiocarbamate) > IC 20 (butyl dithiophosphate) with their respective inhibitory concentration as 47.03, 38.36, and 33.34 μg•g(-1). Besides, soil enzyme activities revealed that these three flotation collectors had an obvious effect on fluorescein diacetate hydrolysis (FDA) enzyme and catalase (CAT) enzyme. The proposed methods can provide meaningful toxicological information of flotation reagents to soil microbes in the view of metabolism and biochemistry, which are consistent and correlated to each other.

Initial growth of Schizolobium parahybae in Brazilian Cerrado soil under liming and mineral fertilization

Directory of Open Access Journals (Sweden)

Ademilson Coneglian

Full Text Available ABSTRACT High prices and the scarcity of hardwoods require the use of alternative wood sources, such as the Guapuruvu (Schizolobium parahybae, an arboreal species native to the Atlantic Forest, which has fast growth and high market potential. However, there is no information on its cultivation in the Brazilian Cerrado. Thus, this study aimed to analyze the contribution of mineral fertilization and liming in a Cerrado soil on the initial growth of Schizolobium parahybae. The experiment was set in a randomized block design, with 4 treatments (Cerrado soil; soil + liming; soil + fertilizer; and soil + fertilizer + liming and 15 replicates. The following variables were analyzed: plant height, stem diameter, number of leaves, total, shoot, leaf, root and stem dry matter, and root/shoot ratio. The obtained data were subjected to the analysis of variance, Tukey test and regression analysis. During the initial growth, Schizolobium parahybae can be cultivated in a Brazilian Cerrado soil only under mineral fertilization, with no need for soil liming.

Influences upon the lead isotopic composition of organic and mineral horizons in soil profiles from the National Soil Inventory of Scotland (2007–09)

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Farmer, John G., E-mail: J.G.Farmer@ed.ac.uk [School of GeoSciences, The University of Edinburgh, Crew Building, Alexander Crum Brown Road, Edinburgh, EH9 3FF Scotland (United Kingdom); Graham, Margaret C. [School of GeoSciences, The University of Edinburgh, Crew Building, Alexander Crum Brown Road, Edinburgh, EH9 3FF Scotland (United Kingdom); Eades, Lorna J. [School of Chemistry, The University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh, EH9 3FJ Scotland (United Kingdom); Lilly, Allan; Bacon, Jeffrey R. [James Hutton Institute, Craigiebuckler, Aberdeen, AB15 8QH Scotland (United Kingdom)

2016-02-15

Some 644 individual soil horizons from 169 sites in Scotland were analyzed for Pb concentration and isotopic composition. There were three scenarios: (i) 36 sites where both top and bottom (i.e. lowest sampled) soil horizons were classified as organic in nature, (ii) 67 with an organic top but mineral bottom soil horizon, and (iii) 66 where both top and bottom soil horizons were mineral. Lead concentrations were greater in the top horizon relative to the bottom horizon in all but a few cases. The top horizon {sup 206}Pb/{sup 207}Pb ratio was lesser (outside analytical error) than the corresponding bottom horizon {sup 206}Pb/{sup 207}Pb ratio at (i) 64%, (ii) 94% and (iii) 73% of sites, and greater at only (i) 8%, (ii) 3% and (iii) 8% of sites. A plot of {sup 208}Pb/{sup 207}Pb vs. {sup 208}Pb/{sup 206}Pb ratios showed that the Pb in organic top (i, ii) and bottom (i) horizons was consistent with atmospherically deposited Pb of anthropogenic origin. The {sup 206}Pb/{sup 207}Pb ratio of the organic top horizon in (ii) was unrelated to the {sup 206}Pb/{sup 207}Pb ratio of the mineral bottom horizon as demonstrated by the geographical variation in the negative shift in the ratio, a result of differences in the mineral horizon values arising from the greater influence of radiogenic Pb in the north. In (iii), the lesser values of the {sup 206}Pb/{sup 207}Pb ratio for the mineral top horizon relative to the mineral bottom horizon were consistent with the presence of anthropogenic Pb, in addition to indigenous Pb, in the former. Mean anthropogenic Pb inventories of 1.5 and 4.5 g m{sup −2} were obtained for the northern and southern halves of Scotland, respectively, consistent with long-range atmospheric transport of anthropogenic Pb (mean {sup 206}Pb/{sup 207}Pb ratio ~ 1.16). For cultivated agricultural soils (Ap), this corresponded to about half of the total Pb inventory in the top 30 cm of the soil column. - Highlights: • Pb isotope ratios were determined for 644

Microbes Persist: Using a Systems Biology Approach to Reveal How the Soil Microbiome Shapes Soil Organic Matter

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Pett-Ridge, J.

2017-12-01

Soils store more carbon than the atmosphere and terrestrial vegetation combined, yet the factors that control its persistence remain elusive. Recent insights have overturned the long-held assumption that carbon stability depends mostly on chemical `recalcitrance' of soil organic matter (SOM). Instead, an emerging paradigm emphasizes how environmental drivers like temperature and moisture, soil minerals, and microbial ecology interact to control SOM formation, stabilization, and turnover. Detailed spectroscopic and isotopic (14C) analyses of mineral-associated SOM show that the oldest carbon in soil may be easily broken down and respired in the laboratory, and that it biochemically resembles microbial cells and metabolites far more than plant material. This places microbial ecophysiology at the center of the soil carbon persistence question. Microbial cells likely interact with mineral surfaces as part of an ecological strategy to condition their environment (e.g. biofilm formation or extracellular enzyme production), and their diverse cellular components likely associate with minerals after cells die. Collectively, these microbial characteristics - metabolic activities, population growth strategies, and cellular biochemistry - can be thought of as `soil ecophysiological traits'. This presentation will explore potential traits that may be fruitful targets for studies evaluating the persistence and importance of microbial products as SOM precursors, and will highlight results showing that soil mineral type influences the microbial communities that colonize mineral surfaces, as well as the quantity and type of mineral-associated carbon that accumulates. I will propose a series of integrated approaches that used together can examine how genomic capacity and activities of soil microbiomes are shaped by edaphic conditions (moisture, temperature, redox regimes) and fundamentally affect the terrestrial soil C pool.

Differential controls on soil carbon density and mineralization among contrasting forest types in a temperate forest ecosystem

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You, Ye-Ming; Wang, Juan; Sun, Xiao-Lu; Tang, Zuo-Xin; Zhou, Zhi-Yong; Sun, Osbert Jianxin

2016-01-01

Understanding the controls on soil carbon dynamics is crucial for modeling responses of ecosystem carbon balance to global change, yet few studies provide explicit knowledge on the direct and indirect effects of forest stands on soil carbon via microbial processes. We investigated tree species, soil, and site factors in relation to soil carbon density and mineralization in a temperate forest of central China. We found that soil microbial biomass and community structure, extracellular enzyme activities, and most of the site factors studied varied significantly across contrasting forest types, and that the associations between activities of soil extracellular enzymes and microbial community structure appeared to be weak and inconsistent across forest types, implicating complex mechanisms in the microbial regulation of soil carbon metabolism in relation to tree species. Overall, variations in soil carbon density and mineralization are predominantly accounted for by shared effects of tree species, soil, microclimate, and microbial traits rather than the individual effects of the four categories of factors. Our findings point to differential controls on soil carbon density and mineralization among contrasting forest types and highlight the challenge to incorporate microbial processes for constraining soil carbon dynamics in global carbon cycle models. PMID:26925871

Ofloxacin sorption in soils after long-term tillage: The contribution of organic and mineral compositions

International Nuclear Information System (INIS)

Zhou, Dandan; Chen, Bingfa; Wu, Min; Liang, Ni; Zhang, Di; Li, Hao; Pan, Bo

2014-01-01

Intensive human activities in agricultural areas resulted in significant alteration of soil properties, which consequently change their interactions with various contaminants. This process needs to be incorporated in contaminant behavior prediction and their risk assessment. However, the relevant study is missing. This work was designed to examine the change of soil properties and ofloxacin (OFL) sorption after tillage. Soil samples were collected in Yuanyang, Mengzi, and Dianchi areas with different agricultural activities. Although the mineral compositions of soils from Yuanyang and Dianchi differed greatly, these compositions are similar after tillage, especially for paddy soils. Soil pH decreased generally after OFL sorption, suggesting that ion exchange of OFL with protons in soil organic matter (SOM) was important for OFL sorption. However, a positive relationship between SOM and OFL sorption was not observed. On the contrary, increased SOM decreased OFL sorption when soils from the same geological location were compared. Generally speaking, tillage activities or dense vegetations greatly decreased OFL sorption. The higher OFL sorption in B horizon than A horizon suggested limited leaching of OFL through soil columns. The summed sorption calculated based on the sorption of individual soil components and their percentages in soils was higher than the intact soil. This phenomenon may be understood from the interactions between soil components, such as the coating of SOM on mineral particles. This study emphasizes that soil should be treat as a dynamic environmental matrix when assessing antibiotic behaviors and risks, especially in the area with intense human activities. - Highlights: • Mineral compositions tend to be similar after tillage. • Increased SOM decreases OFL sorption for soils from the same geological location. • Tillage activities or dense vegetations greatly decrease OFL sorption. • The summed sorption of individual soil components is

Medicinal significance of vegetables cultivated over minerals supplemented soil

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Bangash, J.A.; Arif, M.; Khan, F.; Khan, F.; Khan, A.S.

2010-01-01

Three winter season vegetables Fenugreek/Methi (Trigonella-foenum-graceum), Sarson (Brassica-campestris-var-sarson) and Garlic (Allium-sativum) were included in the present study to determine some of their mineral components and see if some of their mineral (Cr, Zn, Mn, Cu, Mg and Fe) content could be increased by supplementation through their roots. Thus calculated amount of Cr, Zn, Mn, Cu, Mg and Fe salts (as fertilizer) were applied in solution form to the roots of vegetables in different concentration as individual or in combinations. These vegetables were grown from seeds in the soil plot. After harvesting vegetables were dried, acid digested and analyzed for Cr, Mn, Zn, Cu, Fe and Mg on Hitachi Zeeman Japan Z-8000, Atomic Absorption Spectrophotometer. Thus in Fenugreek/Methi (Trigonella-foenum-graceum) total increase of Cr, Zn, Mn, Mg and Fe recorded was (10, 94, 10, 256 and 520) mg/Kg dry weight basis; in Sarson (Brassica-campestris-var-sarson) total increase of Cr, Zn, Mn and Mg recorded was (12, 30, 22 and 424) mg/Kg dry weight basis and ( Garlic) (Allium-sativum) total increase of Cr, Zn, Mn, Cu, Mg and Fe recorded was (14, 28, 4, 4, 116 and 10) mg/Kg dry weight basis. From the present study it can be concluded that by changing the soil minerals environment the uptake of required mineral content of vegetables, perhaps could be enhanced. This could play important role in management of diabetes control and also in the elimination of other deficiency diseases like anemia. (author)

Soil respiration and net N mineralization along a climate gradient in Maine

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Jeffery A. Simmons; Ivan J. Fernandez; Russell D. Briggs

1996-01-01

Our objective was to determine the influence of temperature and moisture on soil respiration and net N mineralization in northeastern forests. The study consisted of sixteen deciduous stands located along a regional climate gradient within Maine. A significant portion of the variance in net N mineralization (41 percent) and respiration (33 percent) was predicted by...

[Distribution and sources of oxygen and sulfur heterocyclic aromatic compounds in surface soil of Beijing, China].

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He, Guang-Xiu; Zhang, Zhi-Huan; Peng, Xu-Yang; Zhu, Lei; Lu, Ling

2011-11-01

62 surface soil samples were collected from different environmental function zones in Beijing. Sulfur and oxygen heterocyclic aromatic compounds were detected by GC/MS. The objectives of this study were to identify the composition and distribution of these compounds, and discuss their sources. The results showed that the oxygen and sulfur heterocyclic aromatic compounds in the surface soils mainly contained dibenzofuran, methyl- and C2-dibenzofuran series, dibenzothiophene, methyl-, C2- and C3-dibenzothiophene series and benzonaphthothiophene series. The composition and distribution of the oxygen and sulfur heterocyclic aromatic compounds in the surface soil samples varied in the different environmental function zones, of which some factories and the urban area received oxygen and sulfur heterocyclic aromatic compounds most seriously. In Beijing, the degree of contamination by oxygen and sulfur heterocyclic aromatic compounds in the north surface soil was higher than that in the south. There were preferable linear correlations between the concentration of dibenzofuran series and fluorene series, as well as the concentration of dibenzothiophene series and dibenzofuran series. The oxygen and sulfur heterocyclic aromatic compounds in the surface soil were mainly derived from combustion products of oil and coal and direct input of mineral oil, etc. There were some variations in pollution sources of different environmental function zones.

Relationship among Phosphorus Circulation Activity, Bacterial Biomass, pH, and Mineral Concentration in Agricultural Soil

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Dinesh Adhikari

2017-12-01

Full Text Available Improvement of phosphorus circulation in the soil is necessary to enhance phosphorus availability to plants. Phosphorus circulation activity is an index of soil’s ability to supply soluble phosphorus from organic phosphorus in the soil solution. To understand the relationship among phosphorus circulation activity; bacterial biomass; pH; and Fe, Al, and Ca concentrations (described as mineral concentration in this paper in agricultural soil, 232 soil samples from various agricultural fields were collected and analyzed. A weak relationship between phosphorus circulation activity and bacterial biomass was observed in all soil samples (R2 = 0.25, and this relationship became significantly stronger at near-neutral pH (6.0–7.3; R2 = 0.67. No relationship between phosphorus circulation activity and bacterial biomass was observed at acidic (pH < 6.0 or alkaline (pH > 7.3 pH. A negative correlation between Fe and Al concentrations and phosphorus circulation activity was observed at acidic pH (R2 = 0.72 and 0.73, respectively, as well as for Ca at alkaline pH (R2 = 0.64. Therefore, bacterial biomass, pH, and mineral concentration should be considered together for activation of phosphorus circulation activity in the soil. A relationship model was proposed based on the effects of bacterial biomass and mineral concentration on phosphorus circulation activity. The suitable conditions of bacterial biomass, pH, and mineral concentration for phosphorus circulation activity could be estimated from the relationship model.

Soil Organic Carbon and Its interaction with Minerals in Two Hillslopes with Different Climates and Erosion Processes

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Wang, X.; Yoo, K.; Wackett, A. A.; Gutknecht, J.; Amundson, R.; Heimsath, A. M.

2017-12-01

Climate and topography have been widely recognized as important factors regulating soil organic carbon (SOC) dynamics but their interactive effects on SOC storage and its pools remain poorly constrained. Here we aimed to evaluate SOC storages and carbon-mineral interactions along two hillslope transects with moderately different climates (MAP: 549 mm vs. 816 mm) in Southeastern Australia. We sampled soil along the convex (eroding)-to-convergent (depositional) continuum at each hillslope transect and conducted size and density fractionation of these samples. In responses to the difference in climate factor, SOC inventories of eroding soils were twice as large at the wetter site compared with the drier site but showed little difference between two sites in depositional soils. These trends in SOC inventories were primarily controlled by SOC concentrations and secondarily by soil thicknesses. Similar patterns were observed for mineral associated organic carbon (MOC), and the abundances of MOC were controlled by the two independently operating processes affecting MOC concentration and fine-heavy fraction minerals. The contents and species of secondary clay and iron oxide minerals, abundances of particulate organic carbon, and bioturbation affected MOC concentrations. In contrast, the abundances of fine-heavy fraction minerals were impacted by erosion mechanisms that uniquely responded to regional- and micro- climate conditions. Consequently, topographic influences on SOC inventories and carbon-mineral interactions were more strongly pronounced in the drier climate where vegetation and erosion mechanisms were sensitive to microclimate. Our results highlight the significance of understanding topography and erosional processes in capturing climatic effects on soil carbon dynamics.

Spectroscopic quantification of soil phosphorus forms by 31P-NMR after nine years of organic or mineral fertilization

International Nuclear Information System (INIS)

Gatiboni, Luciano Colpo; Brunetto, Gustavo; Rheinheimer, Danilo dos Santos; Kaminski, Joao; Flores, Alex Fabiani Claro; Lima, Maria Angelica Silveira; Girotto, Eduardo; Copetti, Andre Carlos Cruz; Pandolfo, Carla Maria; Veiga, Milton

2013-01-01

Long-standing applications of mineral fertilizers or types of organic wastes such as manure can cause phosphorus (P) accumulation and changes in the accumulated P forms in the soil. The objective of this research was to evaluate the forms of P accumulated in soils treated with mineral fertilizer or different types of manure in a long-term experiment. Soil was sampled from the 0-5 cm layer of plots fertilized with five different nutrient sources for nine years: 1) control without fertilizer; 2) mineral fertilizer at recommended rates for local conditions; 3) 5 t ha -1 year -1 of moist poultry litter; 4) 60 m 3 ha -1 year -1 of liquid cattle manure and 5) 40 m 3 ha -1 year -1 of liquid swine manure. The 31 P-NMR spectra of soil extracts detected the following P compounds: orthophosphate, pyrophosphate, inositol phosphate, glycerophosphate, and DNA. The use of organic or mineral fertilizer over nine years did not change the soil P forms but influenced their concentration. Fertilization with mineral or organic fertilizers stimulated P accumulation in inorganic forms. Highest inositol phosphate levels were observed after fertilization with any kind of manure and highest organic P concentration in glycerophosphate form in after mineral or no fertilization. (author)

Assessing the use of composts from multiple sources based on the characteristics of carbon mineralization in soil.

Science.gov (United States)

Zhang, Xu; Zhao, Yue; Zhu, Longji; Cui, Hongyang; Jia, Liming; Xie, Xinyu; Li, Jiming; Wei, Zimin

2017-12-01

In order to improve soil quality, reduce wastes and mitigate climate change, it is necessary to understand the balance between soil organic carbon (SOC) accumulation and depletion under different organic waste compost amended soils. The effects of proportion (5%, 15%, 30%), compost type (sewage sludge (SS), tomato stem waste (TSW), municipal solid waste (MSW), kitchen waste (KW), cabbage waste (CW), peat (P), chicken manure (CM), dairy cattle manure (DCM)) and the black soil (CK). Their initial biochemical composition (carbon, nitrogen, C:N ratio) on carbon (C) mineralization in soil amended compost have been investigated. The CO 2 -C production of different treatments were measured to indicate the levels of carbon (C) mineralization during 50d of laboratory incubation. And the one order E model (M1E) was used to quantify C mineralization kinetics. The results demonstrated that the respiration and C mineralization of soil were promoted by amending composts. The C mineralization ability increased when the percentage of compost added to the soil also increased and affected by compost type in the order CM>KW, CW>SS, DCM, TSW>MSW, P>CK at the same amended level. Based on the values of C 0 and k 1 from M1E model, a management method in agronomic application of compost products to the precise fertilization was proposed. The SS, DCM and TSW composts were more suitable in supplying fertilizer to the plant. Otherwise, The P and MSW composts can serve the purpose of long-term nutrient retention, whereas the CW and KW composts could be used as soil remediation agent. Copyright © 2017 Elsevier Ltd. All rights reserved.

Effect of Mineral and Humic Substances on Tailing Soil Properties and Nutrient Uptake by Pennisetum purpureum Schumach

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Adhe Phoppy Wira Etika

2015-05-01

Full Text Available Tin mining produces a by-product sand tailing from soil leaching with characteristic low pH and total organic carbon, and can be reclaimed by providing a suitable ameliorant. When available in situ, ameliorant materials can be economically used as they are required in large amounts. Fortunately, Bangka Belitung has sample stock of such kaolinite-rich minerals that can be utilized for improving soil chemical properties. Extracted organic materials, such as humic substances, can also be utilized as they influence the complex soil reactions, and promote plant growth. Thus, this study aimed to assess the effects of mineral, humic materials and interaction of both material on soil chemical properties and nutrient uptake of Pennisetum purpureum Schumach. A completely randomized design with 2 factors and 3 replications each was employed. Factor 1 was mineral matter is 0; 420; 840; 1.260 Mg ha-1 while Factor 2 was humic material is 0; 0.46; 0.92; 1.38 kg C ha-1. Air-dried samples of tailing were applied with oil palm compost then mixed evenly with mineral and humic materials. Penissetum purpureum Schumach was planted after 4 weeks incubation, and maintained for another 4 weeks. The results demonstrated that the addition of mineral matter significantly increased soil organic carbon content, total N, exchangeable K, Fe, Mn and boosted nutrient - total Ca, Mg and Mn – uptake of the plant. But the application of humic material increased only soil organic carbon content. The interaction of both materials only lowered soil pH.

Ice and mineral licks used by caribou in winter

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Douglas C. Heard

1990-09-01

Full Text Available In winter, barren-ground caribou obtain minerals from ice and soil licks. Between December and April we have seen caribou cratering on the surface of frozen lakes and licking the ice. Ice samples from eight licks on four lakes contained concentrations of calcium, magnesium, sodium, potassium, phosphorus, chloride and sulphate many times higher than in the surrounding unlicked ice or than would be expected in lake water. Soil licks being used in March and June had high concentrations of calcium, magnesium, sodium phosphorus and potassium. In winter caribou may be seeking supplements of all of the major mineral elements (calcium, magnesium, sodium and potassium at ice and soil licks because lichens, their staple winter diet, are low in minerals and may also reduce the absorption of some minerals.

Evaluation of Soils Contained in Mineral Tailings at Junin Lake

International Nuclear Information System (INIS)

Gomez, Javier; Fabian, Julio; Vela, Mariano

2008-01-01

The Junin National Reserve is located between the provinces of Junin and Pasco, Sierra Central, high land of Peru. It was analyzed 20 samples from different geographic locations soil of the Reserve. The results showed us that there are pollutants minerals very harmful to the environment because of some of the centers miners deposited the tailings in the vicinity of the nature reserve. The techniques used for characterization of mineralogical soil were: neutron activation analysis, x-ray fluorescence and spectroscopy Moessbauer by transmission. The analysis done by the method of X-ray fluorescence indicate the presence of Rubidium, tungsten, calcium, iron, nickel, copper, zinc, gold and zirconium. With spectroscopy Moessbauer technique was observed the presence a higher proportion of paramagnetic iron; while thanks to neutron activation analysis, besides these elements, it was observed the presence of Molybdenum, Manganese and a high concentration of arsenic. (authors)

Evaluation of Soils Contained in Mineral Tailings at Junin Lake

Energy Technology Data Exchange (ETDEWEB)

Gomez, Javier [Instituto de Investigacion de Fisica, Av. Universitaria s/n, Lima (Peru); Fabian, Julio; Vela, Mariano [Instituto Peruano de Energia Nuclear, Av. Canada 1470, San Borja, Lima (Peru)

2008-07-01

The Junin National Reserve is located between the provinces of Junin and Pasco, Sierra Central, high land of Peru. It was analyzed 20 samples from different geographic locations soil of the Reserve. The results showed us that there are pollutants minerals very harmful to the environment because of some of the centers miners deposited the tailings in the vicinity of the nature reserve. The techniques used for characterization of mineralogical soil were: neutron activation analysis, x-ray fluorescence and spectroscopy Moessbauer by transmission. The analysis done by the method of X-ray fluorescence indicate the presence of Rubidium, tungsten, calcium, iron, nickel, copper, zinc, gold and zirconium. With spectroscopy Moessbauer technique was observed the presence a higher proportion of paramagnetic iron; while thanks to neutron activation analysis, besides these elements, it was observed the presence of Molybdenum, Manganese and a high concentration of arsenic. (authors)

Mineralização do carbono da palha de aveia e dejetos de suínos aplicados na superfície ou incorporados ao solo Carbon mineralization of straw and pig manure with and without incorporation in soil

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Sandro José Giacomini

2008-12-01

Full Text Available A mineralização do C de dejetos de suínos e de palhas de cereais é um processo ainda relativamente pouco estudado no Brasil. O objetivo deste trabalho foi avaliar a mineralização do C da palha de aveia, dos dejetos líquidos de suínos e da cama sobreposta de suínos, aplicados na superfície ou incorporados em um Argissolo Vermelho distrófico arênico, em condições de laboratório. Utilizou-se o delineamento inteiramente casualizado, com quatro repetições dos seguintes tratamentos: solo; solo + palha incorporada; solo + palha em superfície; solo + cama sobreposta incorporada; solo + cama sobreposta em superfície; solo + dejetos líquidos incorporados; solo + dejetos líquidos em superfície; solo + palha + dejetos líquidos incorporados; e solo + palha + dejetos líquidos em superfície. Durante 80 dias de incubação, a emissão de CO2 foi medida continuamente. Ao final desse período, observou-se que foram mineralizados 59 % do C dos dejetos líquidos e apenas 23 % do C da cama sobreposta. A incorporação dos materiais orgânicos ao solo não resultou em maior mineralização do C, quando comparado à permanência desses na superfície do solo. O N amoniacal, aplicado com os dejetos líquidos de suínos, não aumentou a mineralização do C da palha de aveia.The C mineralization of pig manure and cereal straw is still relatively little studied in Brazil. The aim of this work was to evaluate C mineralization of oat straw, pig slurry and pig deep-litter, applied on the surface or incorporated in a Hapludalf soil, in laboratory conditions. The experiment was a completely randomized design with four replications of the following treatments: soil; soil + incorporated straw; soil + surface straw; soil + incorporated pig deep-litter; soil + surface pig deep-litter; soil + incorporated pig slurry; soil + surface pig slurry; soil + incorporated straw + pig slurry; and soil + surface straw + pig slurry. During the 80 days of incubation

Rapid Turnover and Minimal Accretion of Mineral Soil Carbon During 60-Years of Pine Forest Growth on Previously Cultivated Land

Science.gov (United States)

Richter, D., Jr.; Mobley, M. L.; Billings, S. A.; Markewitz, D.

2016-12-01

At the Calhoun Long-Term Soil-Ecosystem field experiment (1957-present), reforestation of previously cultivated land over fifty years nearly doubled soil organic carbon (SOC) in surface soils (0 to 7.5-cm) but these gains were offset by significant SOC losses in subsoils (35 to 60-cm). Nearly all of the accretions in surface soils amounted to gains in light fraction SOC, whereas losses at depth were associated with silt and clay-sized particles. These changes are documented in the Calhoun Long-Term Soil-Ecosystem (LTSE) study that resampled soil from 16 plots about every five years and archived all soil samples from four soil layers within the upper 60-cm of mineral soil. We combined soil bulk density, density fractionation, stable isotopes, and radioisotopes to explore changes in SOC and soil organic nitrogen (SON) associated with five decades of the growth of a loblolly pine secondary forest. Isotopic signatures showed relatively large accumulations of contemporary forest-derived carbon in surface soils, and no accumulation of forest-derived carbon in subsoils. We interpret results to indicate that land-use change from cotton fields to secondary pine forests drove soil biogeochemical and hydrological changes that enhanced root and microbial activity and SOM decomposition in subsoils. As pine stands matured and are now transitioning to mixed pines and hardwoods, demands on soil organic matter for nutrients to support aboveground growth has eased due to pine mortality, and bulk SOM and SON and their isotopes in subsoils have stabilized. We anticipate major changes in the next fifty years as 1957 pine trees transition to hardwoods. This study emphasizes the importance of long-term experiments and deep soil measurements when characterizing SOC and SON responses to land use change. There is a remarkable paucity of E long-term soil data deeper than 30 cm.

Complexity of clay mineral formation during 120,000 years of soil development along the Franz Josef chronosequence, New Zealand

International Nuclear Information System (INIS)

Dietel, J.; Dohrmann, R.; Guggenberger, G.; Meyer-Stueve, S.; Turner, S.; Schippers, A.; Kaufhold, S.; Butz-Braun, R.; Condron, L.M.; Mikutta, R.

2017-01-01

Weathering of primary silicates to secondary clay minerals over time affects multiple soil functions such as the accumulation of organic matter and nutrient cations. However, the extent of clay mineral (trans)formation as a function of soil development is poorly understood. In this study, the degree of weathering of sediments along a 120 kyr soil formation gradient was investigated using X-ray diffraction, Fourier transform infrared spectroscopy and X-ray fluorescence spectroscopy. Irrespective of site age, mica and chlorite were the dominant clay minerals. During weathering, a remarkable suite of transitional phases such as vermiculite and several interstratifications with vermiculitic, smectitic, chloritic and micaceous layers developed. The degree of weathering was correlated with soil pH and depletion of K, Ca, Na, Fe and Al, regarding both soil depth and site age. Kaolinite occurred especially at the 120 kyr site, indicating slow formation via transitional phases. The findings of this study revealed that long-term soil development caused complex clay mineral assemblages, both temporally and spatially, and linking this variability to soil functioning warrants further research. (author).

Contact angles at the water-air interface of hydrocarbon-contaminated soils and clay minerals

Science.gov (United States)

Sofinskaya, O. A.; Kosterin, A. V.; Kosterina, E. A.

2016-12-01

Contact angles at the water-air interface have been measured for triturated preparations of clays and soils in order to assess changes in their hydrophobic properties under the effect of oil hydrocarbons. Tasks have been to determine the dynamics of contact angle under soil wetting conditions and to reveal the effect of chemical removal of organic matter from soils on the hydrophilicity of preparations. The potentialities of static and dynamic drop tests for assessing the hydrophilic-hydrophobic properties of soils have been estimated. Clays (kaolinite, gumbrine, and argillite) have been investigated, as well as plow horizons of soils from the Republic of Tatarstan: heavy loamy leached chernozem, medium loamy dark gray forest soil, and light loamy soddy-calcareous soil. The soils have been contaminated with raw oil and kerosene at rates of 0.1-3 wt %. In the uncontaminated and contaminated chernozem, capillary water capacity has been maintained for 250 days. The contact angles have been found to depend on the degree of dispersion of powdered preparation, the main type of clay minerals in the soil, the presence and amount of oxidation-resistant soil organic matter, and the soil-water contact time. Characteristic parameters of mathematical models for drop behavior on triturated preparations have been calculated. Contamination with hydrocarbons has resulted in a reliable increase in the contact angles of soil preparations. The hydrophobization of soil surface in chernozem is more active than in soils poorer in organic matter. The complete restoration of the hydrophilic properties of soils after hydrocarbon contamination is due to the oxidation of easily oxidizable organic matter at the low content of humus, or to wetting during several months in the absence of the mazut fraction.

Pathogenic prion protein is degraded by a manganese oxide mineral found in soils

Science.gov (United States)

Russo, F.; Johnson, C.J.; McKenzie, D.; Aiken, Judd M.; Pedersen, J.A.

2009-01-01

Prions, the aetiological agents of transmissible spongiform encephalopathies, exhibit extreme resistance to degradation. Soil can retain prion infectivity in the environment for years. Reactive soil components may, however, contribute to the inactivation of prions in soil. Members of the birnessite family of manganese oxides (MnO2) rank among the strongest natural oxidants in soils. Here, we report the abiotic degradation of pathogenic prion protein (PrPTSE) by a synthetic analogue of naturally occurring birnessite minerals. Aqueous MnO2 suspensions degraded the PrPTSE as evidenced by decreased immunoreactivity and diminished ability to seed protein misfolding cyclic amplification reactions. Birnessite-mediated PrPTSE degradation increased as a solution's pH decreased, consistent with the pH-dependence of the redox potential of MnO2. Exposure to 5.6 mg MnO2 ml-1 (PrPTSE:MnO2=1 : 110) decreased PrPTSE levels by ???4 orders of magnitude. Manganese oxides may contribute to prion degradation in soil environments rich in these minerals. ?? 2009 SGM.

Relative nitrogen mineralization and nitrification potentials in relation to soil chemistry in oak forest soils along a historical deposition gradient

Science.gov (United States)

Ralph E. J. Boerner; Elaine Kennedy Sutherland

1996-01-01

This study quantified soil nutrient status and N mineralization/nitrification potentials in soils of oak-dominated, unmanaged forest stands in seven USDA Forest Service experimental forests (EF) ranging along a historical and current acidic deposition gradient from southern Illinois to central West Virginia.

Response of hydrolytic enzyme activities and nitrogen mineralization to fertilizer and organic matter application in subtropical paddy soils

Science.gov (United States)

Kader, Mohammed Abdul; Yeasmin, Sabina; Akter, Masuda; Sleutel, Steven

2016-04-01

Driving controllers of nitrogen (N) mineralization in paddy soils, especially under anaerobic soil conditions, remain elusive. The influence of exogenous organic matter (OM) and fertilizer application on the activities of five relevant enzymes (β-glucosaminidase, β-glucosidase, L-glutaminase, urease and arylamidase) was measured in two long-term field experiments. One 18-years field experiment was established on a weathered terrace soil with a rice-wheat crop rotation at the Bangabandhu Sheikh Mujibur Rahman Agricultural University (BSMRAU) having five OM treatments combined with two mineral N fertilizer levels. Another 30-years experiment was established on a young floodplain soil with rice-rice crop rotation at the Bangladesh Agricultural University (BAU) having eight mineral fertilizer treatments combined with organic manure. At BSMRAU, N fertilizer and OM amendments significantly increased all enzyme activities, suggesting them to be primarily determined by substrate availability. At BAU, non-responsiveness of β-glucosidase activity suggested little effect of the studied fertilizer and OM amendments on general soil microbial activity. Notwithstanding probably equal microbial demand for N, β-glucosaminidase and L-glutaminase activities differed significantly among the treatments (P>0.05) and followed strikingly opposite trends and correlations with soil organic N mineralization. So enzymatic pathways to acquire N differed by treatment at BAU, indicating differences in soil N quality and bio-availability. L-glutaminase activity was significantly positively correlated to the aerobic and anaerobic N mineralization rates at both field experiments. Combined with negative correlations between β-glucosaminidase activity and N mineralization rates, it appears that terminal amino acid NH2 hydrolysis was a rate-limiting step for soil N mineralization at BAU. Future investigations with joint quantification of polyphenol accumulation and binding of N, alongside an

Clay minerals, metallic oxides and oxy-hydroxides and soil organic carbon distribution within soil aggregates in temperate forest soils

Science.gov (United States)

Gartzia-Bengoetxea, Nahia; Fernández-Ugalde, Oihane; Virto, Iñigo; Arias-González, Ander

2017-04-01

Soil mineralogy is of primary importance for key environmental services provided by soils like carbon sequestration. However, current knowledge on the effects of clay mineralogy on soil organic carbon (SOC) stabilization is based on limited and conflicting data. In this study, we investigated the relationship between clay minerals, metallic oxides and oxy-hydroxides and SOC distribution within soil aggregates in mature Pinus radiata D.Don forest plantations. Nine forest stands located in the same geographical area of the Basque Country (North of Spain) were selected. These stands were planted on different parent material (3 on each of the following: sandstone, basalt and trachyte). There were no significant differences in climate and forest management among them. Moreover, soils under these plantations presented similar content of clay particles. We determined bulk SOC storage, clay mineralogy, the content of Fe-Si-Al-oxides and oxyhydroxides and the distribution of organic C in different soil aggregate sizes at different soil depths (0-5 cm and 5-20 cm). The relationship between SOC and abiotic factors was investigated using a factor analysis (PCA) followed by stepwise regression analysis. Soils developed on sandstone showed significantly lower concentration of SOC (29 g C kg-1) than soils developed on basalts (97 g C kg-1) and trachytes (119 g C kg-1). The soils on sandstone presented a mixed clay mineralogy dominated by illite, with lesser amounts of hydroxivermiculite, hydrobiotite and kaolinite, and a total absence of interstratified chlorite/vermiculite. In contrast, the major crystalline clay mineral identified in the soils developed on volcanic rocks was interstratified chlorite/vermiculite. Nevertheless, no major differences were observed between basaltic and trachytic soils in the clay mineralogy. The selective extraction of Fe showed that the oxalate extractable iron was significantly lower in soils on sandstone (3.7%) than on basalts (11.2%) and

Spatial variability of isoproturon mineralizing activity within an agricultural field: geostatistical analysis of simple physicochemical and microbiological soil parameters.

Science.gov (United States)

El Sebai, T; Lagacherie, B; Soulas, G; Martin-Laurent, F

2007-02-01

We assessed the spatial variability of isoproturon mineralization in relation to that of physicochemical and biological parameters in fifty soil samples regularly collected along a sampling grid delimited across a 0.36 ha field plot (40 x 90 m). Only faint relationships were observed between isoproturon mineralization and the soil pH, microbial C biomass, and organic nitrogen. Considerable spatial variability was observed for six of the nine parameters tested (isoproturon mineralization rates, organic nitrogen, genetic structure of the microbial communities, soil pH, microbial biomass and equivalent humidity). The map of isoproturon mineralization rates distribution was similar to that of soil pH, microbial biomass, and organic nitrogen but different from those of structure of the microbial communities and equivalent humidity. Geostatistics revealed that the spatial heterogeneity in the rate of degradation of isoproturon corresponded to that of soil pH and microbial biomass.

Forest soil mineral weathering rates: use of multiple approaches

Science.gov (United States)

Randy K. Kolka; D.F. Grigal; E.A. Nater

1996-01-01

Knowledge of rates of release of base cations from mineral dissolution (weathering) is essential to understand ecosystem elemental cycling. Although much studied, rates remain enigmatic. We compared the results of four methods to determine cation (Ca + Mg + K) release rates at five forested soils/sites in the northcentral U.S.A. Our premise was that multiple...

Revegetation of Acid Rock Drainage (ARD) Producing Slope Surface Using Phosphate Microencapsulation and Artificial Soil

Science.gov (United States)

Kim, Jae Gon

2017-04-01

Oxidation of sulfides produces acid rock drainage (ARD) upon their exposure to oxidation environment by construction and mining activities. The ARD causes the acidification and metal contamination of soil, surface water and groundwater, the damage of plant, the deterioration of landscape and the reduction of slope stability. The revegetation of slope surface is one of commonly adopted strategies to reduce erosion and to increase slope stability. However, the revegetation of the ARD producing slope surface is frequently failed due to its high acidity and toxic metal content. We developed a revegetation method consisting of microencapsualtion and artificial soil in the laboratory. The revegetation method was applied on the ARD producing slope on which the revegetation using soil coverage and seeding was failed and monitored the plant growth for one year. The phosphate solution was applied on sulfide containing rock to form stable Fe-phosphate mineral on the surface of sulfide, which worked as a physical barrier to prevent contacting oxidants such as oxygen and Fe3+ ion to the sulfide surface. After the microencapsulation, two artificial soil layers were constructed. The first layer containing organic matter, dolomite powder and soil was constructed at 2 cm thickness to neutralize the rising acidic capillary water from the subsurface and to remove the dissolved oxygen from the percolating rain water. Finally, the second layer containing seeds, organic matter, nutrients and soil was constructed at 3 cm thickness on the top. After application of the method, the pH of the soil below the artificial soil layer increased and the ARD production from the rock fragments reduced. The plant growth showed an ordinary state while the plant died two month after germination for the previous revegetation trial. No soil erosion occurred from the slope during the one year field test.

Thallium speciation and extractability in a thallium- and arsenic-rich soil developed from mineralized carbonate rock.

Science.gov (United States)

Voegelin, Andreas; Pfenninger, Numa; Petrikis, Julia; Majzlan, Juraj; Plötze, Michael; Senn, Anna-Caterina; Mangold, Stefan; Steininger, Ralph; Göttlicher, Jörg

2015-05-05

We investigated the speciation and extractability of Tl in soil developed from mineralized carbonate rock. Total Tl concentrations in topsoil (0-20 cm) of 100-1000 mg/kg are observed in the most affected area, subsoil concentrations of up to 6000 mg/kg Tl in soil horizons containing weathered ore fragments. Using synchrotron-based microfocused X-ray fluorescence spectrometry (μ-XRF) and X-ray absorption spectroscopy (μ-XAS) at the Tl L3-edge, partly Tl(I)-substituted jarosite and avicennite (Tl2O3) were identified as Tl-bearing secondary minerals formed by the weathering of a Tl-As-Fe-sulfide mineralization hosted in the carbonate rock from which the soil developed. Further evidence was found for the sequestration of Tl(III) into Mn-oxides and the uptake of Tl(I) by illite. Quantification of the fractions of Tl(III), Tl(I)-jarosite and Tl(I)-illite in bulk samples based on XAS indicated that Tl(I) uptake by illite was the dominant retention mechanism in topsoil materials. Oxidative Tl(III)uptake into Mn-oxides was less relevant, probably because the Tl loadings of the soil exceeded the capacity of this uptake mechanism. The concentrations of Tl in 10 mM CaCl2-extracts increased with increasing soil Tl contents and decreasing soil pH, but did not exhibit drastic variations as a function of Tl speciation. With respect to Tl in contaminated soils, this study provides first direct spectroscopic evidence for Tl(I) uptake by illite and indicates the need for further studies on the sorption of Tl to clay minerals and Mn-oxides and its impact on Tl solubility in soils.

30 CFR 779.21 - Soil resources information.

Science.gov (United States)

2010-07-01

... 30 Mineral Resources 3 2010-07-01 2010-07-01 false Soil resources information. 779.21 Section 779.21 Mineral Resources OFFICE OF SURFACE MINING RECLAMATION AND ENFORCEMENT, DEPARTMENT OF THE INTERIOR SURFACE COAL MINING AND RECLAMATION OPERATIONS PERMITS AND COAL EXPLORATION SYSTEMS UNDER REGULATORY PROGRAMS SURFACE MINING PERMIT...

Organic horizon and mineral soil mercury along three clear-cut forest chronosequences across the northeastern USA.

Science.gov (United States)

Richardson, Justin B; Petrenko, Chelsea L; Friedland, Andrew J

2017-12-01

Mercury (Hg) is a globally distributed pollutant trace metal that has been increasing in terrestrial environments due to rising anthropogenic emissions. Vegetation plays an important role in Hg sequestration in forested environments, but increasing tree removal for biofuels and wood products may affect this process. The long-term effect of clear-cutting on forest soil Hg remains uncertain, since most studies are limited to measuring changes for event. The chronosequence approach, which substitutes space for time using forest stands of different ages since clear-cutting, allows for investigation of processes occurring over decades to centuries. Here, we utilized three clear-cut forest soil chronosequences across the northeastern USA to understand Hg accumulation and retention over several decades. Total Hg concentrations and pools were quantified for five soil depth increments along three chronosequences. Our results showed Hg concentrations and pools decreased in the initial 20 years following clear-cutting. Mineral soil Hg pools decreased 21-53% (7-14 mg m -2 ) between 1-5-year-old stands and 15-25-year-old stands but mineral soil Hg pools recovered in 55-140-year-old stands to similar values as measured in 1-5-year-old stands. Our study is one of the first to demonstrate a decrease and recovery in Hg pool size. These changes in Hg did not correspond with changes in bulk density, soil C, or pH. We utilized a simple two-box model to determine how different Hg fluxes affected organic and mineral soil horizon Hg pools. Our simple model suggests that changes in litterfall and volatilization rates could have caused the observed changes in organic horizon Hg pools. However, only increases in leaching could reproduce observed decreases to mineral soil Hg pools. Further studies are needed to determine the mechanism of Hg loss from forest soils following clear-cutting.

Nitrogen isotope ratios in surface and sub-surface soil horizons

International Nuclear Information System (INIS)

Rennie, D.A.; Paul, E.A.

1975-01-01

Nitrogen isotope analysis of surface soils and soil-derived nitrate for selected chernozemic and luvisolic soils showed mean delta 15 N values of 11.7 and 11.3, respectively. Isotope enrichment of the total N reached a maximum in the lower B horizon. Sub-soil parent material samples from the one deep profile included in the study indicated a delta 15 N value (NO 3 -N) of 1/3 that of the Ap horizon, at a depth of 180 cm. The delta 15 N of sub-surface soil horizons containing residual fertilizer N were low (-2.2) compared to the surface horizon (9.9). The data reported from this preliminary survey suggest that the natural variations in 15 N abundance between different soils and horizons of the same soil reflect the cumulative effects of soil genesis and soil management. More detailed knowledge and understanding of biological and other processes which control N isotope concentrations in these soils must be obtained before the data reported can be interpreted. (author)

Natural nanoparticles in soils and their role in organic-mineral interactions and cooloid-facilitated transport

NARCIS (Netherlands)

Regelink, I.C.

2014-01-01

Mineral nanoparticles are naturally present in the soil and play an important role in several soil processes. This thesis uses a combination of novel analytical techniques, among which Field-Flow-Fractionation, to study nanoparticles in soil and water samples. The results show that nanoparticles

Gross mineralization of nitrogen in fertile soils. Effects of the tillage system and soil depths

International Nuclear Information System (INIS)

Videla, C.; Echeverria, H.; Studdert, G.

2002-01-01

A greenhouse experiment was carried out with the aim of determining the effect of different tillage systems and soil depths on gross mineralization rates (TMB). The studied soil was a Typic Argiudoll Petrocalcic Paleudoll complex, under: conventional tillage for 23 yr. (PC treatment); no tillage for 6 yr. (PD treatment), and pasture for 4 yr. (P treatment) and 0-10 and 10-20 sampling depths. TMB were estimated through 15 N dilution technique, by addition of labelled (NH 4 ) 2 SO 4 (10% 15 N at. exc.) at days 0, 7, 21 and 35. Twenty-four and 72 h after each addition, N inorganic content and 15 N enrichment of inorganic were determined on 2M KCl extracts in order to estimate the TMB. At 0-10 cm depth, TMB increase until day 21 and decreased afterwards. There were no significant differences between tillage treatments. At 10-20 cm soil depth PC and PD TMB were constant during the whole analysed period. P treatment had a quadratic adjust, with negative linear component. P TMB was lower than PC and PD until day 21 but afterwards it was significantly higher. These results suggest the presence in the pasture of an organic matter fraction, which mineralizes lately but with a high rate. (author)

Centimeter-scale spatial variability in 2-methyl-4-chlorophenoxyacetic acid mineralization increases with depth in agricultural soil

DEFF Research Database (Denmark)

Badawi, Nora; Johnsen, Anders R.; Sørensen, Jan

2013-01-01

Mineralization of organic chemicals in soil is typically studied using large homogenized samples, but little is known about the small-scale spatial distribution of mineralization potential. We studied centimeter-scale spatial distribution of 2-methyl-4-chlorophenoxyacetic acid (MCPA) mineralization...... was mineralized in all samples in the plow layer, but only about 60% in the transition zone immediately below the plow layer showed mineralization; at greater depth even fewer samples showed mineralization. A patchy spatial distribution of mineralization activity was observed from right below the plow layer...... activity at different depths (8-115 cm) in a Danish agricultural soil profi le using a 96-well microplate C-radiorespirometric method for small-volume samples. The heterotrophic microbial population and specifi c MCPA degraders decreased 10- to 100-fold from the plow layer to a depth of 115 cm. MCPA...

Organic nitrogen storage in mineral soil: Implications for policy and management

Energy Technology Data Exchange (ETDEWEB)

Bingham, Andrew H., E-mail: drew_bingham@nps.gov [Air Resources Division, National Park Service, P.O. Box 25287, Denver, CO 80225 (United States); Cotrufo, M. Francesca [Department of Soil and Crop Sciences and Natural Resources Ecology Laboratory, Colorado State University, 200 West Lake Street, Fort Collins, CO 80523 (United States)

2016-05-01

Nitrogen is one of the most important ecosystem nutrients and often its availability limits net primary production as well as stabilization of soil organic matter. The long-term storage of nitrogen-containing organic matter in soils was classically attributed to chemical complexity of plant and microbial residues that retarded microbial degradation. Recent advances have revised this framework, with the understanding that persistent soil organic matter consists largely of chemically labile, microbially processed organic compounds. Chemical bonding to minerals and physical protection in aggregates are more important to long-term (i.e., centuries to millennia) preservation of these organic compounds that contain the bulk of soil nitrogen rather than molecular complexity, with the exception of nitrogen in pyrogenic organic matter. This review examines for the first time the factors and mechanisms at each stage of movement into long-term storage that influence the sequestration of organic nitrogen in the mineral soil of natural temperate ecosystems. Because the factors which govern persistence are different under this newly accepted paradigm we examine the policy and management implications that are altered, such as critical load considerations, nitrogen saturation and mitigation consequences. Finally, it emphasizes how essential it is for this important but underappreciated pool to be better quantified and incorporated into policy and management decisions, especially given the lack of evidence for many soils having a finite capacity to sequester nitrogen. - Highlights: • We review the current framework for long-term nitrogen stabilization in soils. • We highlight the most important factors according to this framework. • We discuss how these factors may influence management and policy decisions.

Dissolution of minerals with rough surfaces

Science.gov (United States)

de Assis, Thiago A.; Aarão Reis, Fábio D. A.

2018-05-01

We study dissolution of minerals with initial rough surfaces using kinetic Monte Carlo simulations and a scaling approach. We consider a simple cubic lattice structure, a thermally activated rate of detachment of a molecule (site), and rough surface configurations produced by fractional Brownian motion algorithm. First we revisit the problem of dissolution of initial flat surfaces, in which the dissolution rate rF reaches an approximately constant value at short times and is controlled by detachment of step edge sites. For initial rough surfaces, the dissolution rate r at short times is much larger than rF ; after dissolution of some hundreds of molecular layers, r decreases by some orders of magnitude across several time decades. Meanwhile, the surface evolves through configurations of decreasing energy, beginning with dissolution of isolated sites, then formation of terraces with disordered boundaries, their growth, and final smoothing. A crossover time to a smooth configuration is defined when r = 1.5rF ; the surface retreat at the crossover is approximately 3 times the initial roughness and is temperature-independent, while the crossover time is proportional to the initial roughness and is controlled by step-edge site detachment. The initial dissolution process is described by the so-called rough rates, which are measured for fixed ratios between the surface retreat and the initial roughness. The temperature dependence of the rough rates indicates control by kink site detachment; in general, it suggests that rough rates are controlled by the weakest microscopic bonds during the nucleation and formation of the lowest energy configurations of the crystalline surface. Our results are related to recent laboratory studies which show enhanced dissolution in polished calcite surfaces. In the application to calcite dissolution in alkaline environment, the minimal values of recently measured dissolution rate spectra give rF ∼10-9 mol/(m2 s), and the calculated rate

Impact of activated carbon, biochar and compost on the desorption and mineralization of phenanthrene in soil

DEFF Research Database (Denmark)

Marchal, Geoffrey; Smith, Kilian E.C.; Rein, Arno

2013-01-01

), biochar or compost. Total amounts of phenanthrene desorbed were similar between the different soils, but the amendment type had a large influence. Complete desorption was observed in the unamended and compost amended soils, but this reduced for biochar (41% desorbed) and AC (8% desorbed). Cumulative...... amounts mineralized were 28% for the unamended control, 19% for compost, 13% for biochar and 4% for AC. Therefore, the effects of the amendments in soil in reducing desorption were also reflected in the extents of mineralization. Modeling was used to analyze key processes, indicating that for the AC...

Element concentrations in surface soils of the Coconino Plateau, Grand Canyon region, Coconino County, Arizona

Science.gov (United States)

Van Gosen, Bradley S.

2016-09-15

This report provides the geochemical analyses of a large set of background soils collected from the surface of the Coconino Plateau in northern Arizona. More than 700 soil samples were collected at 46 widespread areas, sampled from sites that appear unaffected by mineralization and (or) anthropogenic contamination. The soils were analyzed for 47 elements, thereby providing data on metal concentrations in soils representative of the plateau. These background concentrations can be used, for instance, for comparison to metal concentrations found in soils potentially affected by natural and anthropogenic influences on the Coconino Plateau in the Grand Canyon region of Arizona.The soil sampling survey revealed low concentrations for the metals most commonly of environmental concern, such as arsenic, cobalt, chromium, copper, mercury, manganese, molybdenum, lead, uranium, vanadium, and zinc. For example, the median concentrations of the metals in soils of the Coconino Plateau were found to be comparable to the mean values previously reported for soils of the western United States.

Influence of soil properties on the toxicity of TiO₂ nanoparticles on carbon mineralization and bacterial abundance.

Science.gov (United States)

Simonin, Marie; Guyonnet, Julien P; Martins, Jean M F; Ginot, Morgane; Richaume, Agnès

2015-01-01

Information regarding the impact of low concentration of engineered nanoparticles on soil microbial communities is currently limited and the importance of soil characteristics is often neglected in ecological risk assessment. To evaluate the impact of TiO2 nanoparticles (NPs) on soil microbial communities (measured on bacterial abundance and carbon mineralization activity), 6 agricultural soils exhibiting contrasted textures and organic matter contents were exposed for 90 days to a low environmentally relevant concentration or to an accidental spiking of TiO2-NPs (1 and 500mgkg(-1) dry soil, respectively) in microcosms. In most soils, TiO2-NPs did not impact the activity and abundance of microbial communities, except in the silty-clay soil (high OM) where C-mineralization was significantly lowered, even with the low NPs concentration. Our results suggest that TiO2-NPs toxicity does not depend on soil texture but likely on pH and OM content. We characterized TiO2-NPs aggregation and zeta potential in soil solutions, in order to explain the difference of TiO2-NPs effects on soil C-mineralization. Zeta potential and aggregation of TiO2-NPs in the silty-clay (high OM) soil solution lead to a lower stability of TiO2-NP-aggregates than in the other soils. Further experiments would be necessary to evaluate the relationship between TiO2-NPs stability and toxicity in the soil. Copyright © 2014 Elsevier B.V. All rights reserved.

EFFECTS OF NITRIFICATION INHIBITORS ON MINERAL NITROGEN DYNAMICS IN AGRICULTURE SOILS

OpenAIRE

Ferisman Tindaon; Gero Benckiser; ohannes Carl Gottlieb Ottow

2011-01-01

Experiments were conducted under laboratory conditions to elucidate the effect of three nitrification inhibitors viz, 3.4dimethylpyrazo-lephosphate (DMPP), 4-Chlormethylpyrazole (ClMP) and dicyandiamide (DCD) on mineral nitrogen dynamics of (NH4)2SO4 in soil incubated at 25oC in soils. The quantitative determination of ammonium, nitrite and nitrate were carried out spectrophotometrically, while potential denitrify-cation capacity (PDC) was measured gas chromatographically. DMPP, ClMP and DCD ...

Effects of Nitrification Inhibitors on Mineral Nitrogen Dynamics in Agriculture Soils

OpenAIRE

Tindaon, Ferisman; Benckiser, Gero; Ottow, Johannes Carl Gottlieb

2011-01-01

Experiments were conducted under laboratory conditions to elucidate the effect of three nitrification inhibitors viz, 3.4dime-thylpyrazo-lephosphate (DMPP), 4-Chlormethylpyrazole (ClMP) and dicyandiamide (DCD) on mineral nitrogen dynamics of (NH4)2SO4 in soil incubated at 25oC in soils. The quantitative determination of ammonium, nitrite and nitrate were carried out spectrophotometrically, while potential denitrify-cation capacity (PDC) was measured gas chromatographically. DMPP, ClMP and DCD...

Cd Mobility in Anoxic Fe-Mineral-Rich Environments - Potential Use of Fe(III)-Reducing Bacteria in Soil Remediation

Science.gov (United States)

Muehe, E. M.; Adaktylou, I. J.; Obst, M.; Schröder, C.; Behrens, S.; Hitchcock, A. P.; Tylsizczak, T.; Michel, F. M.; Krämer, U.; Kappler, A.

2014-12-01

Agricultural soils are increasingly burdened with heavy metals such as Cd from industrial sources and impure fertilizers. Metal contaminants enter the food chain via plant uptake from soil and negatively affect human and environmental health. New remediation approaches are needed to lower soil metal contents. To apply these remediation techniques successfully, it is necessary to understand how soil microbes and minerals interact with toxic metals. Here we show that microbial Fe(III) reduction initially mobilizes Cd before its immobilization under anoxic conditions. To study how microbial Fe(III) reduction influences Cd mobility, we isolated a new Cd-tolerant, Fe(III)-reducing Geobacter sp. from a heavily Cd-contaminated soil. In lab experiments, this Geobacter strain first mobilized Cd from Cd-loaded Fe(III) hydroxides followed by precipitation of Cd-bearing mineral phases. Using Mössbauer spectroscopy and scanning electron microscopy, the original and newly formed Cd-containing Fe(II) and Fe(III) mineral phases, including Cd-Fe-carbonates, Fe-phosphates and Fe-(oxyhydr)oxides, were identified and characterized. Using energy-dispersive X-ray spectroscopy and synchrotron-based scanning transmission X-ray microscopy, Cd was mapped in the Fe(II) mineral aggregates formed during microbial Fe(III) reduction. Microbial Fe(III) reduction mobilizes Cd prior to its precipitation in Cd-bearing mineral phases. The mobilized Cd could be taken up by phytoremediating plants, resulting in a net removal of Cd from contaminated sites. Alternatively, Cd precipitation could reduce Cd bioavailability in the environment, causing less toxic effects to crops and soil microbiota. However, the stability and thus bioavailability of these newly formed Fe-Cd mineral phases needs to be assessed thoroughly. Whether phytoremediation or immobilization of Cd in a mineral with reduced Cd bioavailability are feasible mechanisms to reduce toxic effects of Cd in the environment remains to be

Soil N mineralization profiles of co-existing woody vegetation islands at the alpine tree line

Czech Academy of Sciences Publication Activity Database

Wang, L.; Godbold, Douglas

2017-01-01

Roč. 136, 5-6 (2017), s. 881-892 ISSN 1612-4669 R&D Projects: GA MŠk(CZ) LO1415 Institutional support: RVO:67179843 Keywords : Tree line * Soil N mineralization * in situ field incubation * Soil N availability * Resin capsule * Woody vegetation islands Subject RIV: DF - Soil Science OBOR OECD: Soil science Impact factor: 2.017, year: 2016

Potential Nitrification and Nitrogen Mineral of Soil in Coffee Agroforestry System with Various Shading Trees

Directory of Open Access Journals (Sweden)

Purwanto .

2007-05-01

Full Text Available The role of shading trees in coffee farms has been well understood to establish suitable condition for the growth of coffee trees, on the other hand their role in nitrogen cycle in coffee farming is not yet well understood. The objectives of this study are to investigate the influence of various legume shading trees on the concentration of soil mineral N (N-NH4 + and N-NO3-, potential nitrification and to study the controlling factors of nitrification under field conditions. This field explorative research was carried out in Sumberjaya, West Lampung. Twelve observation plots covered four land use systems (LUS, i.e. 1 Coffee agroforestry with Gliricidiasepium as shade trees; 2 Coffee agroforestry with Gliricidiaas shade trees and Arachis pintoias cover crops; 3Coffee agroforestry with Paraserianthes falcataria as shade trees; and 4 Mixed/multistrata coffee agroforestry with Gliricidiaand other fruit crops as shade trees. Measurements of soil mineral-N concentration were carried out every three weeks for three months. Results showed that shade tree species in coffee agroforestry significantly affected concentrations of soil NH4 +, NO3- and potential nitrification. Mixed coffee agroforestry had the highest NH4+/N-mineral ratio (7.16% and the lowest potential nitrification (0.13 mg NO2-kg-1 hour -1 compared to other coffee agroforestry systems using single species of leguminous shade trees. Ratio of NH4 + /N-mineral increased 0.8—21% while potential nitrification decreased 55—79% in mixed coffee agroforestry compared to coffee agroforestry with Gliricidia or P. falcatariaas shade trees. Coffee agroforestry with P. falcatariaas shade trees had potential nitrification 53% lower and ratio of NH4 + /N-mineral concentration 20% higher than that with Gliricidia. Coffee agroforestry with P. falcataria as shade trees also had organic C content 17% higher, total N 40% higher, available P 112% higher than that with Gliricidia. The presence of A. pintoiin

Mineralization dynamics in soil fertilized with seaweed-fish waste compost.

Science.gov (United States)

Illera-Vives, Marta; López-Fabal, Adolfo; López-Mosquera, M Elvira; Ribeiro, Henrique M

2015-12-01

Seaweed and fish waste can be composted together to obtain fertilizer with high organic matter and nutrient contents. The nutrients, however, are mostly in organic form and must be mineralized to make them available to plants. The objective of this work was to establish a usage guideline for the compost by studying its mineralization dynamics. Also, the release of inorganic N and C from soil fertilized with the compost was monitored and modelled. C and N were released throughout the assay, to an extent significantly dependent on fertilizer rate. Mineralization of both elements fitted a first-order exponential model, and each fertilizer rate required using a specific fitting model. An increased rate favoured mineralization (especially of carbon). After 90 days, 2.3% of C and 7.7% of N were mineralized (and 23.3% of total nitrogen made plant available) with the higher rate. C mineralization was slow because organic matter in the compost was very stable. On the other hand, the relatively high initial content in mineral N of the compost increased gradually by the effect of mineralization. The amount of N available would suffice to meet the requirements of moderately demanding crops at the lower fertilizer rate, and even those of more demanding crops at the higher rate. © 2015 Society of Chemical Industry.

Stability of the Inherent Target Metallome in Seed Crops and a Mushroom Grown on Soils of Extreme Mineral Spans

Directory of Open Access Journals (Sweden)

Gerhard Gramss

2016-02-01

Full Text Available Extremes in soil mineral supply alter the metallome of seeds much less than that of their herbage. The underlying mechanisms of mineral homeostasis and the “puzzle of seed filling” are not yet understood. Field crops of wheat, rye, pea, and the mushroom Kuehneromyces mutabilis were established on a set of metalliferous uranium mine soils and alluvial sands. Mineral concentrations in mature plants were determined from roots to seeds (and to fungal basidiospores by ICP-MS following microwave digestion. The results referred to the concentrations of soil minerals to illustrate regulatory breaks in their flow across the plant sections. Root mineral concentrations fell to a mean of 7.8% in the lower stem of wheat in proportions deviating from those in seeds. Following down- and up-regulations in the flow, the rachis/seed interface configured with cuts in the range of 1.6%–12% (AsPbUZn and up-regulations in the range of 106%–728% (CuMgMnP the final grain metallome. Those of pea seeds and basidiospores were controlled accordingly. Soil concentration spans of 9–109× in CuFeMnNiZn shrank thereby to 1.3–2× in seeds to reveal the plateau of the cultivar’s desired target metallome. This was brought about by adaptations of the seed:soil transfer factors which increased proportionally in lower-concentrated soils. The plants thereby distinguished chemically similar elements (As/P; Cd/Zn and incorporated even non-essential ones actively. It is presumed that high- and low-concentrated soils may impair the mineral concentrations of phloems as the donors of seed minerals. In an analytical and strategic top performance, essential and non-essential phloem constituents are identified and individually transferred to the propagules in precisely delimited quantities.

Measurement of net nitrogen and phosphorus mineralization in wetland soils using a modification of the resin-core technique

Science.gov (United States)

Noe, Gregory B.

2011-01-01

A modification of the resin-core method was developed and tested for measuring in situ soil N and P net mineralization rates in wetland soils where temporal variation in bidirectional vertical water movement and saturation can complicate measurement. The modified design includes three mixed-bed ion-exchange resin bags located above and three resin bags located below soil incubating inside a core tube. The two inner resin bags adjacent to the soil capture NH4+, NO3-, and soluble reactive phosphorus (SRP) transported out of the soil during incubation; the two outer resin bags remove inorganic nutrients transported into the modified resin core; and the two middle resin bags serve as quality-control checks on the function of the inner and outer resin bags. Modified resin cores were incubated monthly for a year along the hydrogeomorphic gradient through a floodplain wetland. Only small amounts of NH4+, NO3-, and SRP were found in the two middle resin bags, indicating that the modified resin-core design was effective. Soil moisture and pH inside the modified resin cores typically tracked changes in the surrounding soil abiotic environment. In contrast, use of the closed polyethylene bag method provided substantially different net P and N mineralization rates than modified resin cores and did not track changes in soil moisture or pH. Net ammonification, nitrifi cation, N mineralization, and P mineralization rates measured using modified resin cores varied through space and time associated with hydrologic, geomorphic, and climatic gradients in the floodplain wetland. The modified resin-core technique successfully characterized spatiotemporal variation of net mineralization fluxes in situ and is a viable technique for assessing soil nutrient availability and developing ecosystem budgets.

Storage and stability of organic carbon in soils as related to depth, occlusion within aggregates, and attachment to minerals

Directory of Open Access Journals (Sweden)

M. Schrumpf

2013-03-01

Full Text Available Conceptual models suggest that stability of organic carbon (OC in soil depends on the source of plant litter, occlusion within aggregates, incorporation in organo-mineral complexes, and location within the soil profile. Density fractionation is a useful tool to study the relevance of OC stabilization in aggregates and in association with minerals, but it has rarely been applied to full soil profiles. We aim to determine factors shaping the depth profiles of physically unprotected and mineral associated OC and test their relevance for OC stability across a range of European soils that vary in vegetation, soil types, parent material, and land use. At each of the 12 study sites, 10 soil cores were sampled to 60 cm depth and subjected to density separation. Bulk soil samples and density fractions (free light fractions – fLF, occluded light fractions – oLF, heavy fractions – HF were analysed for OC, total nitrogen (TN, δ14C, and Δ14C. Bulk samples were also incubated to determine CO2 evolution per g OC in the samples (specific mineralization rates as an indicator for OC stability. Depth profiles of OC in the light fraction (LF-OC matched those of roots for undisturbed grassland and forest sites, suggesting that roots are shaping the depth distribution of LF-OC. Organic C in the HF declined less with soil depth than LF-OC and roots, especially at grassland sites. The decrease in Δ14C (increase in age of HF-OC with soil depth was related to soil pH as well as to dissolved OC fluxes. This indicates that dissolved OC translocation contributes to the formation of subsoil HF-OC and shapes the Δ14C profiles. The LF at three sites were rather depleted in 14C, indicating the presence of fossil material such as coal and lignite, probably inherited from the parent material. At the other sites, modern Δ14C signatures and positive correlations between specific mineralization rates and fLF-OC indicate the fLF is a potentially available energy and

Thermal Properties of Soils

Science.gov (United States)

1981-12-01

plagio - clase feldspar and pyroxene. The tine fraction may Surface area and its effects contain the clay "sheet" minerals (i.e. kaolinite. illite...Pyroxene, Kaoliniwe Unified By By Ortho. Plagio . amphibole, Basic clay min. Hematite Soil Soil soil petrogr. X.ray clase clase and Igneous and clay and no

Response of Soil Bulk Density and Mineral Nitrogen to Harvesting and Cultural Treatments

Science.gov (United States)

Minyi Zhou; Mason C. Carter; Thomas J. Dean

1998-01-01

The interactive effects of harvest intensity, site preparation, and fertilization on soil compaction and nitrogen mineralization were examined in a loblolly pine (Pinus taeda L.) stand growing on a sandy, well-drained soil in eastern Texas. The experimental design was 2 by 2 by 2 factorial, consisting of two harvesting treatments (mechanical whole-...

Organic carbon and reducing conditions lead to cadmium immobilization by secondary Fe mineral formation in a pH-neutral soil.

Science.gov (United States)

Muehe, E Marie; Adaktylou, Irini J; Obst, Martin; Zeitvogel, Fabian; Behrens, Sebastian; Planer-Friedrich, Britta; Kraemer, Ute; Kappler, Andreas

2013-01-01

Cadmium (Cd) is of environmental relevance as it enters soils via Cd-containing phosphate fertilizers and endangers human health when taken up by crops. Cd is known to associate with Fe(III) (oxyhydr)oxides in pH-neutral to slightly acidic soils, though it is not well understood how the interrelation of Fe and Cd changes under Fe(III)-reducing conditions. Therefore, we investigated how the mobility of Cd changes when a Cd-bearing soil is faced with organic carbon input and reducing conditions. Using fatty acid profiles and quantitative PCR, we found that both fermenting and Fe(III)-reducing bacteria were stimulated by organic carbon-rich conditions, leading to significant Fe(III) reduction. The reduction of Fe(III) minerals was accompanied by increasing soil pH, increasing dissolved inorganic carbon, and decreasing Cd mobility. SEM-EDX mapping of soil particles showed that a minor fraction of Cd was transferred to Ca- and S-bearing minerals, probably carbonates and sulfides. Most of the Cd, however, correlated with a secondary iron mineral phase that was formed during microbial Fe(III) mineral reduction and contained mostly Fe, suggesting an iron oxide mineral such as magnetite (Fe3O4). Our data thus provide evidence that secondary Fe(II) and Fe(II)/Fe(III) mixed minerals could be a sink for Cd in soils under reducing conditions, thus decreasing the mobility of Cd in the soil.

Short-Range-Order Mineral Physical Protection On Black Carbon Stabilization

Science.gov (United States)

Liang, B.; Weng, Y. T.; Wang, C. C.; Song, Y. F.; Lehmann, J.; Wang, C. H.

2015-12-01

Soil organic matter is one of the largest reservoirs in global carbon cycle, and black carbon (BC) represents a chemical resistant component. Black C plays an important role in global climate change. Generally considered recalcitrant due to high aromaticity, the reactive surface and functional groups of BC are crucial for carbon sequestration in soils. Mineral sorption and physical protection is an important mechanism for BC long term stabilization and sequestration in environments. Previous studies on mineral protection of BC were limited to analysis techniques in two-dimensions, for example, by SEM, TEM, and NanoSIMS. Little is known about the scope of organo-mineral association, the in-situ distribution and forms of minerals, and the ultimate interplay of BC and minerals. The aim of this study is to investigate the three-dimensional interaction of organic C and minerals in submicron scale using synchrotron-based Transmission X-ray Microcopy (TXM) and Fourier-Transform Infrared Spectroscopy (FTIR). Abundant poorly-crystallined nano-minerals particles were observed. These short-range-order (SRO) minerals also aggregate into clusters and sheets, and form envelops-like structures on the surface of BC. On top of large surface contact area, the intimate interplay between BC and minerals reinforces the stability of both organic C and minerals, resulting from chemical bonding through cation bridging and ligand exchange. The mineral protection enhances BC stabilization and sequestration and lowers its bioavailability in environment. The results suggest that mineral physical protection for BC sequestration may be more important than previous understanding.

Spectroscopic quantification of soil phosphorus forms by {sup 31}P-NMR after nine years of organic or mineral fertilization

Energy Technology Data Exchange (ETDEWEB)

Gatiboni, Luciano Colpo, E-mail: gatiboni@cav.udesc.br [Universidade Estadual de Santa Catarina (UDESC), Lages, SC (Brazil); Brunetto, Gustavo; Rheinheimer, Danilo dos Santos; Kaminski, Joao; Flores, Alex Fabiani Claro; Lima, Maria Angelica Silveira; Girotto, Eduardo; Copetti, Andre Carlos Cruz, E-mail: danilo.rheinheimer@pq.cnpq.br, E-mail: joao.kaminski@gmail.com, E-mail: acflores@quimica.ufsm.br, E-mail: masl32003@gmail.com, E-mail: girottosolos@gmail.com, E-mail: andrecopetti@yahoo.com.br [Universidade Federal de Santa Maria (UFSM), RS (Brazil); Pandolfo, Carla Maria; Veiga, Milton, E-mail: pandolfo@epagri.sc.gov.br, E-mail: milveiga@epagri.sc.gov.br [Empresa de Pesquisa Agropecuaria e Extensao Rural de Santa Catarina (EPAGRI), Campos Novos, SC (Brazil)

2013-05-15

Long-standing applications of mineral fertilizers or types of organic wastes such as manure can cause phosphorus (P) accumulation and changes in the accumulated P forms in the soil. The objective of this research was to evaluate the forms of P accumulated in soils treated with mineral fertilizer or different types of manure in a long-term experiment. Soil was sampled from the 0-5 cm layer of plots fertilized with five different nutrient sources for nine years: 1) control without fertilizer; 2) mineral fertilizer at recommended rates for local conditions; 3) 5 t ha{sup -1} year{sup -1} of moist poultry litter; 4) 60 m{sup 3} ha{sup -1} year{sup -1} of liquid cattle manure and 5) 40 m{sup 3} ha{sup -1} year{sup -1} of liquid swine manure. The {sup 31}P-NMR spectra of soil extracts detected the following P compounds: orthophosphate, pyrophosphate, inositol phosphate, glycerophosphate, and DNA. The use of organic or mineral fertilizer over nine years did not change the soil P forms but influenced their concentration. Fertilization with mineral or organic fertilizers stimulated P accumulation in inorganic forms. Highest inositol phosphate levels were observed after fertilization with any kind of manure and highest organic P concentration in glycerophosphate form in after mineral or no fertilization. (author)

Mineral and surface issues in oil and gas operations

International Nuclear Information System (INIS)

Vasseur, P.F.

1998-01-01

The Farmers' Advocate Office was created in 1972 to help put Alberta mineral owners on an equal footing with the energy sector. Most mineral owners are at a disadvantage when dealing with the disposition of their minerals because they have little or no knowledge of what they own or what their surface rights are. This paper addresses key features of mineral leasing arrangements in Alberta and explains their potential impact. It also brings to the mineral owner's attention some specific problems and concerns including mineral rights, the lease agreement, signing considerations, length of leases, delayed production payment, drilling rental, royalties, and gas cost allowance. Issues regarding oil and gas production including shut-in wells, off-set clauses , drilling depth, taxes and prepayment for minerals are also discussed from the perspective of a mineral owner

Mineralization of soil-aged isoproturon and isoproturon metabolites by Sphingomonas sp. strain SRS2.

Science.gov (United States)

Johannesen, Helle; Sørensen, Sebastian R; Aamand, Jens

2003-01-01

The aim of the study was to determine the effect of aging of the herbicide isoproturon and its metabolites monodesmethyl-isoproturon and 4-isopropyl-aniline in agricultural soil on their availability to the degrading bacterium Sphingomonas sp. strain SRS2. The 14C-ring-labeled isoproturon, monodesmethyl-isoproturon, and 4-isopropyl-aniline were added to sterilized soil and stored for 1, 49, 71, or 131 d before inoculation with strain SRS2. The availability of the compounds was estimated from the initial mineralization and the amount of 14CO2 recovered after 120 d of incubation. Aging in soil for 131 d reduced the initial mineralization of isoproturon and monodesmethyl-isoproturon and, in the case of isoproturon, also reduced the recovery of 14CO2. Initial mineralization and recovery of 14CO2 from aged 4-isopropyl-aniline were slightly reduced, but less 14CO2 was generally produced than with isoproturon or monodesmethyl-isoproturon. Thus, recovery of 14CO2 from 14C-isoproturon and 14C-monodesmethyl-isoproturon was 50.7 to 64.4% of the initially added 14C, while recovery from 14C-4-isopropyl-aniline was only 11.7 to 17.0%. Sorption measurements revealed similar Freundlich constants (K(f)) for isoproturon and monodesmethyl-isoproturon, whereas K(f) for 4-isopropyl-aniline was more than fivefold greater. The findings imply that in soil, partial degradation of isoproturon to 4-isopropyl-aniline may lead to reduced mineralization of the herbicide due to sorption of the aniline moiety.

Optimization method for quantitative calculation of clay minerals in soil

Indian Academy of Sciences (India)

However, no reliable method for quantitative analysis of clay minerals has been established so far. In this study, an attempt was made to propose an optimization method for the quantitative ... 2. Basic principles. The mineralogical constitution of soil is rather complex. ... K2O, MgO, and TFe as variables for the calculation.

Soil Response to Global Change: Soil Process Domains and Pedogenic Thresholds (Invited)

Science.gov (United States)

Chadwick, O.; Kramer, M. G.; Chorover, J.

2013-12-01

The capacity of soil to withstand perturbations, whether driven by climate, land use change, or spread of invasive species, depends on its chemical composition and physical state. The dynamic interplay between stable, well buffered soil process domains and thresholds in soil state and function is a strong determinant of soil response to forcing from global change. In terrestrial ecosystems, edaphic responses are often mediated by availability of water and its flux into and through soils. Water influences soil processes in several ways: it supports biological production, hence proton-donor, electron-donor and complexing-ligand production; it determines the advective removal of dissolution products, and it can promote anoxia that leads microorganisms to utilize alternative electron acceptors. As a consequence climate patterns strongly influence global distribution of soil, although within region variability is governed by other factors such as landscape age, parent material and human land use. By contrast, soil properties can vary greatly among climate regions, variation which is guided by the functioning of a suite of chemical processes that tend to maintain chemical status quo. This soil 'buffering' involves acid-base reactions as minerals weather and oxidation-reduction reactions that are driven by microbial respiration. At the planetary scale, soil pH provides a reasonable indicator of process domains and varies from about 3.5 to10, globally, although most soils lie between about 4.5 and 8.5. Those that are above 7.5 are strongly buffered by the carbonate system, those that are characterized by neutral pH (7.5-6) are buffered by release of non-hydrolyzing cations from primary minerals and colloid surfaces, and those that are buffered by hydrolytic aluminum on colloidal surfaces. Alkali and alkaline (with the exception of limestone parent material) soils are usually associated with arid and semiarid conditions, neutral pH soils with young soils in both dry and wet

Clay minerals and metal oxides strongly influence the structure of alkane-degrading microbial communities during soil maturation.

Science.gov (United States)

Steinbach, Annelie; Schulz, Stefanie; Giebler, Julia; Schulz, Stephan; Pronk, Geertje J; Kögel-Knabner, Ingrid; Harms, Hauke; Wick, Lukas Y; Schloter, Michael

2015-07-01

Clay minerals, charcoal and metal oxides are essential parts of the soil matrix and strongly influence the formation of biogeochemical interfaces in soil. We investigated the role of these parental materials for the development of functional microbial guilds using the example of alkane-degrading bacteria harbouring the alkane monooxygenase gene (alkB) in artificial mixtures composed of different minerals and charcoal, sterile manure and a microbial inoculum extracted from an agricultural soil. We followed changes in abundance and community structure of alkane-degrading microbial communities after 3 and 12 months of soil maturation and in response to a subsequent 2-week plant litter addition. During maturation we observed an overall increasing divergence in community composition. The impact of metal oxides on alkane-degrading community structure increased during soil maturation, whereas the charcoal impact decreased from 3 to 12 months. Among the clay minerals illite influenced the community structure of alkB-harbouring bacteria significantly, but not montmorillonite. The litter application induced strong community shifts in soils, maturated for 12 months, towards functional guilds typical for younger maturation stages pointing to a resilience of the alkane-degradation function potentially fostered by an extant 'seed bank'.

Adsorption of surface functionalized silica nanoparticles onto mineral surfaces and decane/water interface

International Nuclear Information System (INIS)

Metin, Cigdem O.; Baran, Jimmie R.; Nguyen, Quoc P.

2012-01-01

The adsorption of silica nanoparticles onto representative mineral surfaces and at the decane/water interface was studied. The effects of particle size (the mean diameters from 5 to 75 nm), concentration and surface type on the adsorption were studied in detail. Silica nanoparticles with four different surfaces [unmodified, surface modified with anionic (sulfonate), cationic (quaternary ammonium (quat)) or nonionic (polyethylene glycol (PEG)) surfactant] were used. The zeta potential of these silica nanoparticles ranges from −79.8 to 15.3 mV. The shape of silica particles examined by a Hitachi-S5500 scanning transmission electron microscope (STEM) is quite spherical. The adsorption of all the nanoparticles (unmodified or surface modified) on quartz and calcite surfaces was found to be insignificant. We used interfacial tension (IFT) measurements to investigate the adsorption of silica nanoparticles at the decane/water interface. Unmodified nanoparticles or surface modified ones with sulfonate or quat do not significantly affect the IFT of the decane/water interface. It also does not appear that the particle size or concentration influences the IFT. However, the presence of PEG as a surface modifying material significantly reduces the IFT. The PEG surface modifier alone in an aqueous solution, without the nanoparticles, yields the same IFT reduction for an equivalent PEG concentration as that used for modifying the surface of nanoparticles. Contact angle measurements of a decane droplet on quartz or calcite plate immersed in water (or aqueous nanoparticle dispersion) showed a slight change in the contact angle in the presence of the studied nanoparticles. The results of contact angle measurements are in good agreement with experiments of adsorption of nanoparticles on mineral surfaces or decane/water interface. This study brings new insights into the understanding and modeling of the adsorption of surface-modified silica nanoparticles onto mineral surfaces and

Soil mineral composition matters: response of microbial communities to phenanthrene and plant litter addition in long-term matured artificial soils.

Science.gov (United States)

Babin, Doreen; Vogel, Cordula; Zühlke, Sebastian; Schloter, Michael; Pronk, Geertje Johanna; Heister, Katja; Spiteller, Michael; Kögel-Knabner, Ingrid; Smalla, Kornelia

2014-01-01

The fate of polycyclic aromatic hydrocarbons (PAHs) in soil is determined by a suite of biotic and abiotic factors, and disentangling their role in the complex soil interaction network remains challenging. Here, we investigate the influence of soil composition on the microbial community structure and its response to the spiked model PAH compound phenanthrene and plant litter. We used long-term matured artificial soils differing in type of clay mineral (illite, montmorillonite) and presence of charcoal or ferrihydrite. The soils received an identical soil microbial fraction and were incubated for more than two years with two sterile manure additions. The matured artificial soils and a natural soil were subjected to the following spiking treatments: (I) phenanthrene, (II) litter, (III) litter + phenanthrene, (IV) unspiked control. Total community DNA was extracted from soil sampled on the day of spiking, 7, 21, and 63 days after spiking. Bacterial 16S rRNA gene and fungal internal transcribed spacer amplicons were quantified by qPCR and subjected to denaturing gradient gel electrophoresis (DGGE). DGGE analysis revealed that the bacterial community composition, which was strongly shaped by clay minerals after more than two years of incubation, changed in response to spiked phenanthrene and added litter. DGGE and qPCR showed that soil composition significantly influenced the microbial response to spiking. While fungal communities responded only in presence of litter to phenanthrene spiking, the response of the bacterial communities to phenanthrene was less pronounced when litter was present. Interestingly, microbial communities in all artificial soils were more strongly affected by spiking than in the natural soil, which might indicate the importance of higher microbial diversity to compensate perturbations. This study showed the influence of soil composition on the microbiota and their response to phenanthrene and litter, which may increase our understanding of

Helium Ion Microscopy: A Promising Tool for Probing Biota-Mineral Interfaces

Science.gov (United States)

Lybrand, R.; Zaharescu, D. G.; Gallery, R. E.

2017-12-01

The study of biogeochemical interfaces in soil requires powerful technologies that can enhance our ability to characterize mineral surfaces and interacting organisms at micro- to nanoscale resolutions. We aim to demonstrate potential applications of Helium Ion Microscopy in the earth and ecological sciences using, as an example, samples from a field experiment. We assessed samples deployed for one year along climatic and topographic gradients in two Critical Zone Observatories (CZOs): a desert to mixed conifer forest gradient (Catalina CZO) and a humid hardwood forest (Calhoun CZO). Sterile ground rock (basalt, quartz, and granite; 53-250 µm) was sealed into nylon mesh bags and buried in the surface soils of both CZOs. We employed helium ion and scanning electron microscopies to compare retrieved ground rock samples with sterile unreacted mineral controls in conjunction with the Environmental Molecular Sciences Laboratory at Pacific Northwest National Laboratory, USA. Our work showed early colonization of mesh bag materials by fungal and bacterial organisms from the field systems and identified morphological changes in mineral grains following exposure to the soil environment. Biological specimens observed on grain surfaces exhibited contrasting features depending on mineral type and ecosystem location, including fungal hyphae that varied in length, diameter, and surface morphologies. We also present imagery that provides evidence for incipient stages of mineral transformation at the fungal-mineral interface. Our findings demonstrate that helium ion microscopy can be successfully used to characterize grain features and biological agents of weathering in experimental field samples, representing a promising avenue for research in the biogeosciences. Future directions of this work will couple high resolution imaging with measures of aqueous and solid geochemistry, fungal morphological characterization, and microbial profiling to better understand mineral

Chemical composition of the humus layer, mineral soil and soil solution of 200 forest stands in the Netherlands in 1995

NARCIS (Netherlands)

Leeters, E.E.J.M.; Vries, de W.

2001-01-01

A nationwide assessment of the chemical composition of the soil solid phase and the soil solution in the humus layer and two mineral layers (0-10 cm and 10-30 cm) was made for 200 forest stands in the year 1995. The stands were part of the national forest inventory on vitality, included seven tree

The Thermodynamics of Selenium Minerals in Near-Surface Environments

Directory of Open Access Journals (Sweden)

Vladimir Krivovichev

2017-10-01

Full Text Available Selenium compounds are relatively rare as minerals; there are presently only 118 known mineral species. This work is intended to codify and systematize the data of mineral systems and the thermodynamics of selenium minerals, which are unstable (selenides or formed in near-surface environments (selenites, where the behavior of selenium is controlled by variations of the redox potential and the acidity of solutions at low temperatures and pressures. These parameters determine the migration of selenium and its precipitation as various solid phases. All selenium minerals are divided into four groups—native selenium, oxide, selenides, and oxysalts—anhydrous selenites (I and hydrous selenites and selenates (II. Within each of the groups, minerals are codified according to the minimum number of independent elements necessary to define the composition of the mineral system. Eh–pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 9.0 software package. The Eh–pH diagrams of the Me–Se–H2O systems (where Me = Co, Ni, Fe, Cu, Pb, Zn, Cd, Hg, Ag, Bi, As, Sb, Al and Ca were plotted for the average contents of these elements in acidic waters in the oxidation zones of sulfide deposits. The possibility of the formation of Zn, Cd, Ag and Hg selenites under natural oxidation conditions in near surface environments is discussed.

Inclusion of Solar Elevation Angle in Land Surface Albedo Parameterization Over Bare Soil Surface.

Science.gov (United States)

Zheng, Zhiyuan; Wei, Zhigang; Wen, Zhiping; Dong, Wenjie; Li, Zhenchao; Wen, Xiaohang; Zhu, Xian; Ji, Dong; Chen, Chen; Yan, Dongdong

2017-12-01

Land surface albedo is a significant parameter for maintaining a balance in surface energy. It is also an important parameter of bare soil surface albedo for developing land surface process models that accurately reflect diurnal variation characteristics and the mechanism behind the solar spectral radiation albedo on bare soil surfaces and for understanding the relationships between climate factors and spectral radiation albedo. Using a data set of field observations, we conducted experiments to analyze the variation characteristics of land surface solar spectral radiation and the corresponding albedo over a typical Gobi bare soil underlying surface and to investigate the relationships between the land surface solar spectral radiation albedo, solar elevation angle, and soil moisture. Based on both solar elevation angle and soil moisture measurements simultaneously, we propose a new two-factor parameterization scheme for spectral radiation albedo over bare soil underlying surfaces. The results of numerical simulation experiments show that the new parameterization scheme can more accurately depict the diurnal variation characteristics of bare soil surface albedo than the previous schemes. Solar elevation angle is one of the most important factors for parameterizing bare soil surface albedo and must be considered in the parameterization scheme, especially in arid and semiarid areas with low soil moisture content. This study reveals the characteristics and mechanism of the diurnal variation of bare soil surface solar spectral radiation albedo and is helpful in developing land surface process models, weather models, and climate models.

30 CFR 823.12 - Soil removal and stockpiling.

Science.gov (United States)

2010-07-01

... 30 Mineral Resources 3 2010-07-01 2010-07-01 false Soil removal and stockpiling. 823.12 Section 823.12 Mineral Resources OFFICE OF SURFACE MINING RECLAMATION AND ENFORCEMENT, DEPARTMENT OF THE INTERIOR PERMANENT PROGRAM PERFORMANCE STANDARDS SPECIAL PERMANENT PROGRAM PERFORMANCE STANDARDS-OPERATIONS ON PRIME FARMLAND § 823.12 Soil removal and...

Comparison studies adsorption of thorium and uranium on pure clay minerals and local Malaysian soil sediments

International Nuclear Information System (INIS)

Syed, H.S.

1999-01-01

Adsorption studies of thorium and uranium radionuclides on 9 different pure clay minerals and 4 local Malaysian soil sediments were conducted. Solution containing dissolved thorium and uranium at pH 4.90 was prepared from concentrate sludges from a long term storage facility at a local mineral processing plant. The sludges are considered as low level radioactive wastes. The results indicated that the 9 clay minerals adsorbed more uranium than thorium at pH ranges from 3.74 to 5.74. Two local Malaysian soils were observed to adsorb relatively high concentration of both radionuclides at pH 3.79 to 3.91. The adsorption value 23.27 to 27.04 ppm for uranium and 33.1 to 50.18 ppm for thorium indicated that both soil sediments can be considered as potential enhanced barrier material for sites disposing conditioned wastes containing uranium and thorium. (author)

Soil carbon and nitrogen mineralization under different tillage systems and Permanent Groundcover cultivation between Orange trees

Directory of Open Access Journals (Sweden)

Elcio Liborio Balota

2011-06-01

Full Text Available The objective of this work was to evaluate the alterations in carbon and nitrogen mineralization due to different soil tillage systems and groundcover species for intercropped orange trees. The experiment was established in an Ultisol soil (Typic Paleudults originated from Caiuá sandstone in northwestern of the state of Paraná, Brazil, in an area previously cultivated with pasture (Brachiaria humidicola. Two soil tillage systems were evaluated: conventional tillage (CT in the entire area and strip tillage (ST with a 2-m width, each with different groundcover vegetation management systems. The citrus cultivar utilized was the 'Pera' orange (Citrus sinensis grafted onto a 'Rangpur' lime rootstock. The soil samples were collected at a 0-15-cm depth after five years of experiment development. Samples were collected from under the tree canopy and from the inter-row space after the following treatments: (1 CT and annual cover crop with the leguminous Calopogonium mucunoides; (2 CT and perennial cover crop with the leguminous peanut Arachis pintoi; (3 CT and evergreen cover crop with Bahiagrass Paspalum notatum; (4 CT and cover crop with spontaneous B. humidicola grass vegetation; and (5 ST and maintenance of the remaining grass (pasture of B. humidicola. The soil tillage systems and different groundcover vegetation influenced the C and N mineralization, both under the tree canopy and in the inter-row space. The cultivation of B. humidicola under strip tillage provided higher potential mineralization than the other treatments in the inter-row space. Strip tillage increased the C and N mineralization compared to conventional tillage. The grass cultivation increased the C and N mineralization when compared to the others treatments cultivated in the inter-row space.

Managing for soil carbon sequestration: a modeling framework for decision-making

Science.gov (United States)

Abramoff, Rose; Harden, Jennifer; Georgiou, Katerina; Tang, Jinyun; Torn, Margaret; Riley, William

2017-04-01

In order to plan for responsible soil carbon (C) management, it is important to know how site factors will affect C stabilization. For example, is mineral-associated C vulnerable to climate change, and how do management practices that modify plant inputs affect mineral-associated C? We applied a soil organic carbon (SOC) decomposition model that represents microbial physiology and mineral sorption. The model was able to reproduce large spatial gradients in SOC stocks; model predictions of SOC were highly correlated with SOC observations across an 4000 km transect (R2 > 0.9). We also used a Random Forest algorithm to compare our model predictions with transect data. We applied this model to explore expected changes to SOC across a range of mineral surface properties, mean annual temperature (MAT), and plant input rates. We found that SOC generally increased after plant amendments. Furthermore, the type of amendment (i.e., high vs. low lignin content), soil mineralogy, and climate all affected the sign and magnitude of SOC change over time. In particular, cold sites with low mineral surface availability were most vulnerable to SOC loss, and may benefit most from plant amendments. At all sites, mineral surface saturation reduced the SOC pool's sensitivity to changes in plant inputs. Saturated soils lost a smaller fraction of initial mineral-associated C following warming. We encourage the use of soil carbon models as frameworks to evaluate how particular sites may respond to changes in management and/or climate.

Managing Soil Biota-Mediated Decomposition and Nutrient Mineralization in Sustainable Agroecosystems

Directory of Open Access Journals (Sweden)

Joann K. Whalen

2014-01-01

Full Text Available Transformation of organic residues into plant-available nutrients occurs through decomposition and mineralization and is mediated by saprophytic microorganisms and fauna. Of particular interest is the recycling of the essential plant elements—N, P, and S—contained in organic residues. If organic residues can supply sufficient nutrients during crop growth, a reduction in fertilizer use is possible. The challenge is synchronizing nutrient release from organic residues with crop nutrient demands throughout the growing season. This paper presents a conceptual model describing the pattern of nutrient release from organic residues in relation to crop nutrient uptake. Next, it explores experimental approaches to measure the physical, chemical, and biological barriers to decomposition and nutrient mineralization. Methods are proposed to determine the rates of decomposition and nutrient release from organic residues. Practically, this information can be used by agricultural producers to determine if plant-available nutrient supply is sufficient to meet crop demands at key growth stages or whether additional fertilizer is needed. Finally, agronomic practices that control the rate of soil biota-mediated decomposition and mineralization, as well as those that facilitate uptake of plant-available nutrients, are identified. Increasing reliance on soil biological activity could benefit crop nutrition and health in sustainable agroecosystems.

Predicting soil N mineralization using organic matter fractions and soil properties: A re-analysis of literature data

NARCIS (Netherlands)

Ros, G.H.

2012-01-01

Extractable organic matter (EOM) fractions have been used to assess the capacity of soils to supply nitrogen (N), but their role in N mineralization and their potential to improve agricultural fertilizer management are still under debate. This paper shows evidence that the relationship between EOM

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

International Nuclear Information System (INIS)

Klaminder, J.; Grip, H.; Moerth, C.-M.; Laudon, H.

2011-01-01

Research highlights: → Organic compounds is mineralized during later transport in deep groundwater aquifers. → Carbonic acid generated by this process stimulates dissolution of silicate minerals. → Protons derived from pyrite oxidation also affects weathering in deep groundwater. → The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H 2 CO 3 , produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and δ 18 O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H 2 CO 3 generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO 4 2- in the groundwater during lateral transport and a δ 34 S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km 2 ) as evident by δ 18 O signatures and base cation concentrations that overlap with that of the groundwater.

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

Energy Technology Data Exchange (ETDEWEB)

Klaminder, J., E-mail: jonatan.klaminder@emg.umu.se [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)] [Department of Ecology and Environmental Science, Umea University, SE-901 87 (Sweden); Grip, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden); Moerth, C.-M. [Department of Geological Sciences, Stockholm University, 106 91 Stockholm (Sweden); Laudon, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)

2011-03-15

Research highlights: {yields} Organic compounds is mineralized during later transport in deep groundwater aquifers. {yields} Carbonic acid generated by this process stimulates dissolution of silicate minerals. {yields} Protons derived from pyrite oxidation also affects weathering in deep groundwater. {yields} The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H{sub 2}CO{sub 3}, produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and {delta}{sup 18}O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H{sub 2}CO{sub 3} generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO{sub 4}{sup 2-} in the groundwater during lateral transport and a {delta}{sup 34}S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km{sup 2}) as evident by {delta}{sup 18}O signatures and base cation concentrations that overlap with that of the groundwater.

Surface hydrophilicity of PLGA fibers governs in vitro mineralization and osteogenic differentiation

Energy Technology Data Exchange (ETDEWEB)

Thomas, Minnah; Arora, Aditya; Katti, Dhirendra S., E-mail: dsk@iitk.ac.in

2014-12-01

Interfacial properties of biomaterials play an important role in governing their interaction with biological microenvironments. This work investigates the role of surface hydrophilicity of electrospun poly(lactide-co-glycolide) (PLGA) fibers in determining their biological response. For this, PLGA is blended with varying amounts of Pluronic®F-108 and electrospun to fabricate microfibers with varying surface hydrophilicity. The results of mineralization study in simulated body fluid (SBF) demonstrate a significant enhancement in mineralization with an increase in surface hydrophilicity. While presence of serum proteins in SBF reduces absolute mineral content, mineralization continues to be higher on samples with higher surface hydrophilicity. The results from in vitro cell culture studies demonstrate a marked improvement in mesenchymal stem cell —adhesion, elongation, proliferation, infiltration, osteogenic differentiation and matrix mineralization on hydrophilized fibers. Therefore, hydrophilized PLGA fibers are advantageous both in terms of mineralization and elicitation of favorable cell response. Since most of the polymeric materials being used in orthopedics are hydrophobic in nature, the results from this study have strong implications in the future design of interfaces of such hydrophobic materials. In addition, the work proposes a facile method for the modification of electrospun fibers of hydrophobic polymers by blending with a poloxamer for improved bone tissue regeneration. - Highlights: • Surface hydrophilicity of PLGA modulated by blending with Pluronic F-108. • Hydrophilized fibers support better in vitro mineralization. • Mineralization trends retained in the presence of adsorbed serum proteins. • Hydrophilized fibers promote better cell adhesion and proliferation. • Hydrophilized fibers also enable better osteogenic differentiation.

A New Method of Environmental Assessment and Monitoring of Cu, Zn, As, and Pb Pollution in Surface Soil Using Terricolous Fruticose Lichens

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Yuri Sueoka

2016-12-01

Full Text Available Levels of trace element pollution in surface soil can be estimated using soil analyses and leaching tests. These methods may reveal different results due to the effect of soil properties, such as grain size and mineral composition, on elemental availability. Therefore, this study advocates an alternative method for monitoring and assessment of trace element pollution in surface soil using terricolous fruticose lichens. Lichens growing at abandoned mine sites and unpolluted areas in southwest Japan and their substrata were analyzed using inductively coupled plasma-mass spectrometry and X-ray fluorescence spectrometry to clarify the relationships between Cu, Zn, As, and Pb concentrations in lichens and soils, including their absorption properties. Concentrations of these elements in the lichens were positively correlated with those in the soils regardless of lichen species, location, habitat, or conditions of soils. The analyzed lichens had neither competitive nor antagonistic properties in their elemental absorption, which made them good biomonitors of trace element pollution in surface soil. The distribution maps of average Cu, Zn, As, and Pb concentrations at each sampling region detected almost all of the Cu, Zn, and As pollution of the soils. Therefore, lichens could be used in practical applications to monitor Cu, Zn, and As pollution in surface soils.

30 CFR 783.21 - Soil resources information.

Science.gov (United States)

2010-07-01

... 30 Mineral Resources 3 2010-07-01 2010-07-01 false Soil resources information. 783.21 Section 783.21 Mineral Resources OFFICE OF SURFACE MINING RECLAMATION AND ENFORCEMENT, DEPARTMENT OF THE INTERIOR SURFACE COAL MINING AND RECLAMATION OPERATIONS PERMITS AND COAL EXPLORATION SYSTEMS UNDER REGULATORY PROGRAMS UNDERGROUND MINING PERMIT APPLICATION...

Bacterial diversity in the active stage of a bioremediation system for mineral oil hydrocarbon-contaminated soils.

Science.gov (United States)

Popp, Nicole; Schlömann, Michael; Mau, Margit

2006-11-01

Soils contaminated with mineral oil hydrocarbons are often cleaned in off-site bioremediation systems. In order to find out which bacteria are active during the degradation phase in such systems, the diversity of the active microflora in a degrading soil remediation system was investigated by small-subunit (SSU) rRNA analysis. Two sequential RNA extracts from one soil sample were generated by a procedure incorporating bead beating. Both extracts were analysed separately by generating individual SSU rDNA clone libraries from cDNA of the two extracts. The sequencing results showed moderate diversity. The two clone libraries were dominated by Gammaproteobacteria, especially Pseudomonas spp. Alphaproteobacteria and Betaproteobacteria were two other large groups in the clone libraries. Actinobacteria, Firmicutes, Bacteroidetes and Epsilonproteobacteria were detected in lower numbers. The obtained sequences were predominantly related to genera for which cultivated representatives have been described, but were often clustered together in the phylogenetic tree, and the sequences that were most similar were originally obtained from soils and not from pure cultures. Most of the dominant genera in the clone libraries, e.g. Pseudomonas, Acinetobacter, Sphingomonas, Acidovorax and Thiobacillus, had already been detected in (mineral oil hydrocarbon) contaminated environmental samples. The occurrence of the genera Zymomonas and Rhodoferax was novel in mineral oil hydrocarbon-contaminated soil.

Combining selective sequential extractions, X-Ray Absorption Spectroscopy, and X-Ray Powder Diffraction for Cu (II speciation in soil and mineral phases

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Tatiana Minkina

2017-04-01

Full Text Available Interaction of Cu (II ions with the matrix of soil and mineral phases of layered silicates was assessed by the Miller method of selective sequential fractionation and a set of synchrotron X-ray methods, including X-ray powder diffraction (XRD and X-ray absorption spectroscopy (XANES. It was shown that the input of Cu into Calcic Chernozem in the form of monoxide (CuO and salt (Cu(NO32 affected the transformation of Cu compounds and their affinity for metal-bearing phases. It was found that the contamination of soil with a soluble Cu(II salt increased the bioavailability of the metal and the role of organic matter and Fe oxides in the fixation and retention of Cu. During the incubation of soil with Cu monoxide, the content of the metal in the residual fractions increased, which was related to the possible entry of Cu in the form of isomorphic impurities into silicates, as well as to the incomplete dissolution of exogenic compounds at the high level of their input into the soil. A mechanism for the structural transformation of minerals was revealed, which showed that ion exchange processes result in the sorption of Cu (II ions from the saturated solution by active sites on the internal surface of the lattice of dioctahedral aluminosilicates. Surface hydroxyls at the octahedral aluminum atom play the main role. X-ray diagnostics revealed that excess Cu(II ions are removed from the system due to the formation and precipitation of coarsely crystalline Cu(NO3(OH3.

Calculating carbon mass balance from unsaturated soil columns treated with CaSO₄₋minerals: test of soil carbon sequestration.

Science.gov (United States)

Han, Young-Soo; Tokunaga, Tetsu K

2014-12-01

Renewed interest in managing C balance in soils is motivated by increasing atmospheric concentrations of CO2 and consequent climate change. Here, experiments were conducted in soil columns to determine C mass balances with and without addition of CaSO4-minerals (anhydrite and gypsum), which were hypothesized to promote soil organic carbon (SOC) retention and soil inorganic carbon (SIC) precipitation as calcite under slightly alkaline conditions. Changes in C contents in three phases (gas, liquid and solid) were measured in unsaturated soil columns tested for one year and comprehensive C mass balances were determined. The tested soil columns had no C inputs, and only C utilization by microbial activity and C transformations were assumed in the C chemistry. The measurements showed that changes in C inventories occurred through two processes, SOC loss and SIC gain. However, the measured SOC losses in the treated columns were lower than their corresponding control columns, indicating that the amendments promoted SOC retention. The SOC losses resulted mostly from microbial respiration and loss of CO2 to the atmosphere rather than from chemical leaching. Microbial oxidation of SOC appears to have been suppressed by increased Ca(2+) and SO4(2)(-) from dissolution of CaSO4 minerals. For the conditions tested, SIC accumulation per m(2) soil area under CaSO4-treatment ranged from 130 to 260 g C m(-1) infiltrated water (20-120 g C m(-1) infiltrated water as net C benefit). These results demonstrate the potential for increasing C sequestration in slightly alkaline soils via CaSO4-treatment. Copyright © 2014 Elsevier Ltd. All rights reserved.

Mineralization of organic phosphorus in soil size fractions under different vegetation covers in the north of Rio de Janeiro

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Joice Cleide de Oliveira Rita

2013-10-01

Full Text Available In unfertilized, highly weathered tropical soils, phosphorus (P availability to plants is dependent on the mineralization of organic P (Po compounds. The objective of this study was to estimate the mineralization of total and labile Po in soil size fractions of > 2.0, 2.0-0.25 and 2.0 and 2.0-0.25 mm fractions, respectively. In contrast, there was an average increase of 90 % of total Po in microaggregates of 2.0 (-50 % and < 0.25 mm (-76 % fractions, but labile Po increased by 35 % in the 2.0-0.25 mm fraction. The Po fraction relative to total extracted P and total labile P within the soil size fractions varied with the vegetation cover and incubation time. Therefore, the distribution of P fractions (Pi and Po in the soil size fraction revealed the distinctive ability of the cover species to recycle soil P. Consequently, the potential of Po mineralization varied with the size fraction and vegetation cover. Because Po accounted for most of the total labile P, the P availability to plants was closely related to the mineralization of this P fraction.

A Comparative Analyses of Granulometry, Mineral Composition and Major and Trace Element Concentrations in Soils Commonly Ingested by Humans

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Veronica M. Ngole-Jeme

2015-07-01

Full Text Available This study compared the granulometric properties, mineralogical composition and concentrations of major and trace element oxides of commonly ingested soils (geophagic soil collected from different countries with a view of understanding how varied they may be in these properties and to understand the possible health implications of ingesting them. Soil samples were collected from three different countries (South Africa, Swaziland and Democratic Republic of Congo (DRC and their granulometric properties, concentrations of major and trace element oxides as well as mineralogical composition determined. Differences were observed in the granulometric properties of geophagic soil from the three different countries with most of them having <20% clay content. The soils also showed varied degrees of weathering with values of Chemical Index of Alteration (CIA and Chemical Index of Weathering (CIW being between 60% and 99.9% respectively. The mineral assemblages of the soils from South Africa and Swaziland were dominated by the primary minerals quartz and feldspar whereas soils from DRC had more of kaolinite, a secondary mineral than primary minerals. Soils from DRC were associated with silt, clay, Al2O3, and CIA unlike most samples from South Africa which were associated with SiO2, sand, K2O, CaO, and MgO. The soils from Swaziland were closely associated with silt, H2O and Fe2O3(t. These associations reflect the mineralogy of the samples. These soils are not likely to serve as nutrient supplements because of the low concentrations of the nutrient elements contained. The coarse texture of the samples may also result in dental destruction during mastication. Sieving of the soils before ingestion to remove coarse particles is recommended to reduce the potential health threat associated with the ingestion of coarse-textured soils.

A Comparative Analyses of Granulometry, Mineral Composition and Major and Trace Element Concentrations in Soils Commonly Ingested by Humans

Science.gov (United States)

Ngole-Jeme, Veronica M.; Ekosse, Georges-Ivo E.

2015-01-01

This study compared the granulometric properties, mineralogical composition and concentrations of major and trace element oxides of commonly ingested soils (geophagic soil) collected from different countries with a view of understanding how varied they may be in these properties and to understand the possible health implications of ingesting them. Soil samples were collected from three different countries (South Africa, Swaziland and Democratic Republic of Congo (DRC)) and their granulometric properties, concentrations of major and trace element oxides as well as mineralogical composition determined. Differences were observed in the granulometric properties of geophagic soil from the three different countries with most of them having soils also showed varied degrees of weathering with values of Chemical Index of Alteration (CIA) and Chemical Index of Weathering (CIW) being between 60% and 99.9% respectively. The mineral assemblages of the soils from South Africa and Swaziland were dominated by the primary minerals quartz and feldspar whereas soils from DRC had more of kaolinite, a secondary mineral than primary minerals. Soils from DRC were associated with silt, clay, Al2O3, and CIA unlike most samples from South Africa which were associated with SiO2, sand, K2O, CaO, and MgO. The soils from Swaziland were closely associated with silt, H2O and Fe2O3(t). These associations reflect the mineralogy of the samples. These soils are not likely to serve as nutrient supplements because of the low concentrations of the nutrient elements contained. The coarse texture of the samples may also result in dental destruction during mastication. Sieving of the soils before ingestion to remove coarse particles is recommended to reduce the potential health threat associated with the ingestion of coarse-textured soils. PMID:26264010

Conventional intensive logging promotes loss of organic carbon from the mineral soil.

Science.gov (United States)

Dean, Christopher; Kirkpatrick, James B; Friedland, Andrew J

2017-01-01

There are few data, but diametrically opposed opinions, about the impacts of forest logging on soil organic carbon (SOC). Reviews and research articles conclude either that there is no effect, or show contradictory effects. Given that SOC is a substantial store of potential greenhouse gasses and forest logging and harvesting is routine, resolution is important. We review forest logging SOC studies and provide an overarching conceptual explanation for their findings. The literature can be separated into short-term empirical studies, longer-term empirical studies and long-term modelling. All modelling that includes major aboveground and belowground biomass pools shows a long-term (i.e. ≥300 years) decrease in SOC when a primary forest is logged and then subjected to harvesting cycles. The empirical longer-term studies indicate likewise. With successive harvests the net emission accumulates but is only statistically perceptible after centuries. Short-term SOC flux varies around zero. The long-term drop in SOC in the mineral soil is driven by the biomass drop from the primary forest level but takes time to adjust to the new temporal average biomass. We show agreement between secondary forest SOC stocks derived purely from biomass information and stocks derived from complex forest harvest modelling. Thus, conclusions that conventional harvests do not deplete SOC in the mineral soil have been a function of their short time frames. Forest managers, climate change modellers and environmental policymakers need to assume a long-term net transfer of SOC from the mineral soil to the atmosphere when primary forests are logged and then undergo harvest cycles. However, from a greenhouse accounting perspective, forest SOC is not the entire story. Forest wood products that ultimately reach landfill, and some portion of which produces some soil-like material there rather than in the forest, could possibly help attenuate the forest SOC emission by adding to a carbon pool in

Modeling the influence of organic acids on soil weathering

Science.gov (United States)

Lawrence, Corey R.; Harden, Jennifer W.; Maher, Kate

2014-01-01

Biological inputs and organic matter cycling have long been regarded as important factors in the physical and chemical development of soils. In particular, the extent to which low molecular weight organic acids, such as oxalate, influence geochemical reactions has been widely studied. Although the effects of organic acids are diverse, there is strong evidence that organic acids accelerate the dissolution of some minerals. However, the influence of organic acids at the field-scale and over the timescales of soil development has not been evaluated in detail. In this study, a reactive-transport model of soil chemical weathering and pedogenic development was used to quantify the extent to which organic acid cycling controls mineral dissolution rates and long-term patterns of chemical weathering. Specifically, oxalic acid was added to simulations of soil development to investigate a well-studied chronosequence of soils near Santa Cruz, CA. The model formulation includes organic acid input, transport, decomposition, organic-metal aqueous complexation and mineral surface complexation in various combinations. Results suggest that although organic acid reactions accelerate mineral dissolution rates near the soil surface, the net response is an overall decrease in chemical weathering. Model results demonstrate the importance of organic acid input concentrations, fluid flow, decomposition and secondary mineral precipitation rates on the evolution of mineral weathering fronts. In particular, model soil profile evolution is sensitive to kaolinite precipitation and oxalate decomposition rates. The soil profile-scale modeling presented here provides insights into the influence of organic carbon cycling on soil weathering and pedogenesis and supports the need for further field-scale measurements of the flux and speciation of reactive organic compounds.

Effects of apple branch biochar on soil C mineralization and nutrient cycling under two levels of N.

Science.gov (United States)

Li, Shuailin; Liang, Chutao; Shangguan, Zhouping

2017-12-31

The incorporation of biochar into soil has been proposed as a strategy for enhancing soil fertility and crop productivity. However, there is limited information regarding the responses of soil respiration and the C, N and P cycles to the addition of apple branch biochar at different rates to soil with different levels of N. A 108-day incubation experiment was conducted to investigate the effects of the rate of biochar addition (0, 1, 2 and 4% by mass) on soil respiration and nutrients and the activities of enzymes involved in C, N and P cycling under two levels of N. Our results showed that the application of apple branch biochar at rates of 2% and 4% increased the C-mineralization rate, while biochar amendment at 1% decreased the C-mineralization rate, regardless of the N level. The soil organic C and microbial biomass C and P contents increased as the rate of biochar addition was increased to 2%. The biochar had negative effects on β-glucosidase, N-acetyl-β-glucosaminidase and urease activity in N-poor soil but exerted a positive effect on all of these factors in N-rich soil. Alkaline phosphatase activity increased with an increase in the rate of biochar addition, but the available P contents after all biochar addition treatments were lower than those obtained in the treatments without biochar. Biochar application at rates of 2% and 4% reduced the soil nitrate content, particularly in N-rich soil. Thus, apple branch biochar has the potential to sequester C and improve soil fertility, but the responses of soil C mineralization and nutrient cycling depend on the rate of addition and soil N levels. Copyright © 2017 Elsevier B.V. All rights reserved.

Reforestation in southern China: revisiting soil N mineralization and nitrification after 8 years restoration

Science.gov (United States)

Mo, Qifeng; Li, Zhi'An; Zhu, Weixing; Zou, Bi; Li, Yingwen; Yu, Shiqin; Ding, Yongzhen; Chen, Yao; Li, Xiaobo; Wang, Faming

2016-01-01

Nitrogen availability and tree species selection play important roles in reforestation. However, long-term field studies on the effects and mechanisms of tree species composition on N transformation are very limited. Eight years after tree seedlings were planted in a field experiment, we revisited the site and tested how tree species composition affects the dynamics of N mineralization and nitrification. Both tree species composition and season significantly influenced the soil dissolved organic carbon (DOC) and nitrogen (DON). N-fixing Acacia crassicarpa monoculture had the highest DON, and 10-mixed species plantation had the highest DOC. The lowest DOC and DON concentrations were both observed in Eucalyptus urophylla monoculture. The tree species composition also significantly affected net N mineralization rates. The highest rate of net N mineralization was found in A. crassicarpa monoculture, which was over twice than that in Castanopsis hystrix monoculture. The annual net N mineralization rates of 10-mixed and 30-mixed plantations were similar as that of N-fixing monoculture. Since mixed plantations have good performance in increasing soil DOC, DON, N mineralization and plant biodiversity, we recommend that mixed species plantations should be used as a sustainable approach for the restoration of degraded land in southern China.

The Mineralosphere Concept: Mineralogical Control of the Distribution and Function of Mineral-associated Bacterial Communities.

Science.gov (United States)

Uroz, Stephane; Kelly, Laura Catherine; Turpault, Marie-Pierre; Lepleux, Cendrella; Frey-Klett, Pascale

2015-12-01

Soil is composed of a mosaic of different rocks and minerals, usually considered as an inert substrata for microbial colonization. However, recent findings suggest that minerals, in soils and elsewhere, favour the development of specific microbial communities according to their mineralogy, nutritive content, and weatherability. Based upon recent studies, we highlight how bacterial communities are distributed on the surface of, and in close proximity to, minerals. We also consider the potential role of the mineral-associated bacterial communities in mineral weathering and nutrient cycling in soils, with a specific focus on nutrient-poor and acidic forest ecosystems. We propose to define this microbial habitat as the mineralosphere, where key drivers of the microbial communities are the physicochemical properties of the minerals. Copyright © 2015 Elsevier Ltd. All rights reserved.

Mineral cycling in soil and litter arthropod food chains. Progress report, November 1, 1979-October 31, 1980

International Nuclear Information System (INIS)

Crossley, D.A. Jr.

1980-01-01

Recent progress and current status are reported for research concerned with mineral element dynamics in soil arthropod food chains. Research is performed within the larger context of terrestrial decomposition systems, in which soil arthropods may act as regulators of nutrient dynamics during decomposition. Research is measuring rates of nutrient accumulation and excretion by using radioactive tracer techniques with radioactive analogs of nutrients. Experimental measurement of radioactive tracer excretion and nutrient element pools are reported for soil microarthropods, using new methods of counting and microprobe elemental analysis. Research on arthropod-fungal relations is utilizing high-efficiency extraction followed by dissection of 13 x 13 cm soil blocks. A two-component excretion model is reported for Cobalt-60 in earthworms (Eisenia foetida), demonstrating that no assimilation of cobalt occurs from the mineral soil fraction but is entirely from organic matter. Collection of data sets on soil arthropod communities and abundances is completed

Wood strength loss as a measure of decomposition in northern forest mineral soil

Science.gov (United States)

Martin Jurgensen; David Reed; Deborah Page-Dumroese; Peter Laks; Anne Collins; Glenn Mroz; Marek Degorski

2006-01-01

Wood stake weight loss has been used as an index of wood decomposition in mineral soil, but it may not give a reliable estimate in cold boreal forests where decomposition is very slow.Various wood stake strength tests have been used as surrogates of weight loss, but little is known on which test would give the best estimate of decomposition over a variety of soil...

Nitrogen mineralization in forestry-drained peatland soils in the Stołowe Mountains National Park (Central Sudetes Mts

Directory of Open Access Journals (Sweden)

Glina Bartłomiej

2016-06-01

Full Text Available The aim of this work was to determine the intensity of nitrogen mineralization in forestry drained ombrotrophic peatland soils in the Stołowe Mountains National Park, SW Poland. Additionally discussion about the shallow organic soils classification according to Polish Soil Classification (2011 is presented. For the study three research transects were established on forestry drained ombrotrophic peatlands in the Stołowe Mountains. Each of the transect consisted of four (site A and B or five (site C sampling plots. Sampling was conducted in the year 2012. The soil samples for the basic soil properties analysis were sampled in April, whereas undisturbed soil samples were collected in stainless steel rings (100 cm3 every 10 cm in April (spring, July (summer and October (autumn to show the seasonal dynamics of nitrogen mineralization. Statistical analysis showed that the content of N-NH4 was mainly determined by actual soil moisture and precipitation rate, whereas the content of N-NO3 was positively correlated with air temperature. Among investigated peatlands the highest concentrations of mineral nitrogen forms was observed in the Długie Mokradło bog, situated on the Skalniak Plateau-summit. Additionally, the results obtained showed that implementation of new subtype: shallow fibric peat soils (in Polish: gleby torfowe fibrowe płytkie within the type of peat soils (in polish: gleby torfowe should be considered during developing of the next update of Polish Soil Classification.

Areal variability of the mineral soil cover in a reclaimed soda waste dumping site

Directory of Open Access Journals (Sweden)

Klatka Sławomir

2017-03-01

Full Text Available Areal variability of the mineral soil cover in a reclaimed soda waste dumping site. This paper provides an analysis of the areal variability of the thickness and selected physical and chemical properties of the mineral cover formed in the process of settling ponds reclamation at the former Krakow Soda Plant “Solvay”. The topsoil is intended to provide a substrate for plants, therefore, its quality is the main determinant of the development for herbaceous and woody vegetation. Areal variability of the topsoil parameters was determined by kriging. In the context of the envisaged direction of management of the settling ponds, the analysis showed that electrical conductivity, thickness of the soil cover and the sand fraction content have potentially the highest impact on the diversification of vegetation. Understanding the spatial variability of the soil cover parameters, that are essential for vegetation, may contribute to increasing the efficiency of biological reclamation and also to cost reduction. Precise selection of the areas unsuitable for plant growth makes it possible to improve soil parameters on limited areas similarly as in the precision agriculture.

Organic farming and cover crops as an alternative to mineral fertilizers to improve soil physical properties

Science.gov (United States)

Sánchez de Cima, Diego; Luik, Anne; Reintam, Endla

2015-10-01

For testing how cover crops and different fertilization managements affect the soil physical properties in a plough based tillage system, a five-year crop rotation experiment (field pea, white potato, common barley undersown with red clover, red clover, and winter wheat) was set. The rotation was managed under four different farming systems: two conventional: with and without mineral fertilizers and two organic, both with winter cover crops (later ploughed and used as green manure) and one where cattle manure was added yearly. The measurements conducted were penetration resistance, soil water content, porosity, water permeability, and organic carbon. Yearly variations were linked to the number of tillage operations, and a cumulative effect of soil organic carbon in the soil as a result of the different fertilization amendments, organic or mineral. All the systems showed similar tendencies along the three years of study and differences were only found between the control and the other systems. Mineral fertilizers enhanced the overall physical soil conditions due to the higher yield in the system. In the organic systems, cover crops and cattle manure did not have a significant effect on soil physical properties in comparison with the conventional ones, which were kept bare during the winter period. The extra organic matter boosted the positive effect of crop rotation, but the higher number of tillage operations in both organic systems counteracted this effect to a greater or lesser extent.

Application of remedy studies to the development of a soil washing pilot plant that uses mineral processing technology: a practical experience

International Nuclear Information System (INIS)

Richardson, W.S.; Phillips, C.R.; Hicks, R.; Luttrell, J.; Cox, C.

1999-01-01

Soil washing employing mineral processing technology to treat radionuclide-contaminated soils has been examined as a remedy alternative to the exclusive excavation, transportation, and disposal of the soil. Successful application depends on a thorough remedy study, employing a systematic tiered approach that is efficient, self-limiting, and cost effective. The study includes: (1) site and soil characterization to determine the basic mineral and physical properties of both the soil and contaminants and to identify their relative associations; (2) treatment studies to evaluate the performance of process units for contaminant separation; (3) conceptual process design to develop a treatment pilot plant; and (4) engineering design to construct, test, and optimize the actual full-scale plant. A pilot plant using soil washing technology for the treatment of radium-contaminated soil was developed, tested, and demonstrated. The plant used particle-size separation to produced a remediated product that represented approximately 50% of the contaminated soil. Subsequently, it was modified for more effective performance and application to soil with alternate characteristics; it awaits further testing. The economic analysis of soil washing using the pilot plant as a model indicates that a remedy plan based on mineral processing technology is very competitive with the traditional alternative employing excavation, transportation, and disposal exclusively, even when disposal costs are modest or when recovery of remediated soil during treatment is low. This paper reviews the tiered approach as it applies to mineral processing technology to treat radionuclide-contaminated soils and a pilot plant developed to test the soil washing process. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

Surface characterization of bacterial cells relevant to the mineral industry

NARCIS (Netherlands)

Sharma, PK; Rao, KH

Bacteria belonging to the Acidithiobacilli group are widely used in the mineral processing industry in bioleaching and biobeneficiation operations. Paenibacillus polymyxa has also found application in biobeneficiation studies. Microbial adhesion to mineral surface is an essential step,for both

Variations in the patterns of soil organic carbon mineralization and microbial communities in response to exogenous application of rice straw and calcium carbonate

International Nuclear Information System (INIS)

Feng, Shuzhen; Huang, Yuan; Ge, Yunhui; Su, Yirong; Xu, Xinwen; Wang, Yongdong; He, Xunyang

2016-01-01

The addition of exogenous inorganic carbon (CaCO 3 ) and organic carbon has an important influence on soil organic carbon (SOC) mineralization in karst soil, but the microbial mechanisms underlying the SOC priming effect are poorly understood. We conducted a 100-day incubation experiment involving four treatments of the calcareous soil in southwestern China's karst region: control, 14 C-labeled rice straw addition, 14 C-labeled CaCO 3 addition, and a combination of 14 C-labeled rice straw and CaCO 3 . Changes in soil microbial communities were characterized using denaturing gradient gel electrophoresis with polymerase chain reaction (PCR-DGGE) and real-time quantitative PCR (q-PCR). Both 14 C-rice straw and Ca 14 CO 3 addition stimulated SOC mineralization, suggesting that organic and inorganic C affected SOC stability. Addition of straw alone had no significant effect on bacterial diversity; however, when the straw was added in combination with calcium carbonate, it had an inhibitory effect on bacterial and fungal diversity. At the beginning of the experimental period, exogenous additives increased bacterial abundance, although at the end of the 100-day incubation bacterial community abundance had gradually declined. Incubation time, exogenous input, and their interaction significantly affected SOC mineralization (in terms of priming and the cumulative amount of mineralization), microbial biomass carbon (MBC), and microbial community abundance and diversity. Moreover, the key factors influencing SOC mineralization were MBC, bacterial diversity, and soil pH. Overall, these findings support the view that inorganic C is involved in soil C turnover with the participation of soil microbial communities, promoting soil C cycling in the karst region. - Highlights: • Different patterns of 14 C-rice straw and Ca 14 CO 3 addition on positive priming effects of SOC mineralization. • Inorganic C is involved in soil C cycling with the participation of soil microbial

Neutron probe measurement of soil water content close to soil surface

International Nuclear Information System (INIS)

Faleiros, M.C.; Ravelo S, A.; Souza, M.D. de

1993-01-01

The problem of neutron probe soil water content measurements close to soil surface is analysed from the spatial variability and also from the slow neutron loss to the atmosphere points of view. Results obtained on a dark red latosol of the county of Piracicaba, SP, indicate the possibility of precisely measuring the neutron sphere of influence when different media are used on soil surface. (author). 7 refs, 5 figs, 1 tab

Mineralization and Transfer Processes of 14C-labeled Pesticides in Outdoor Lysimeters

International Nuclear Information System (INIS)

Grundmann, Sabine; Doerfler, Ulrike; Ruth, Bernhard; Loos, Christine; Wagner, Tobias; Karl, Heidrun; Munch, Jean Charles; Schroll, Reiner

2008-01-01

A recently designed two-chamber-lysimeter-test-system allows the detailed investigation of degradation, transport and transfer processes of 14 C-labeled substances in soil-plant-atmosphere-systems under outdoor conditions. With this test system it is feasible to distinguish between 14 C-emissions from soil surfaces and 14 C-emissions from plant surfaces in soil monoliths under real environmental conditions. Special soil humidity sensors allow the measurement of soil water content near to the soil surface, in 1 and 5 cm depth. The behavior of organic chemicals can be followed for a whole vegetation period and a mass balance for the applied chemical can be established. Some selected results of the herbicides isoproturon and glyphosate - using the two-chamber-lysimeter-test-system - are presented to demonstrate its applicability for the identification and quantification of the processes that govern pesticide behavior in soil-plant-systems. Mineralization of 14 C-isoproturon was very different in four different soils; the mineralization capacity of the soils ranged from 2 to 60%. Leaching of isoproturon in general was very low, but depending on the soil type and environmental conditions isoproturon and its metabolites could be leached via preferential flow, especially shortly after application. For the herbicide 14 C-glyphosate no accumulation of residues in the soil and no leaching of the residues to deeper soil layers could be observed after three applications. Glyphosate was rapidly degraded to AMPA in the soil. Glyphosate and AMPA were accumulated in soy bean nodules

Studies on 14C-extractable residue, 14C-bound residue and mineralization of 14C-labeled chlorsulfuron in soils

International Nuclear Information System (INIS)

Ye Qingfu; Sun Jinhe; Qi Wenyuan; Wu Jianmin

2003-01-01

The purpose of the present study was to investigate 14 C-extractable residue ( 14 C-ER), 14 C-bound residue ( 14 C-BR) and mineralization of 14 C-labeled chlorsulfuron in soils by using isotope technique. The main factors affecting 14 C-BR formation and the distribution pattern of 14 C-BR in humus were also discussed in details. The results were as follows: (1) The 14 C-ER content of 14 C-chlorsulfuron in seven kinds of soil was positively related to soil pH and negatively related to clay content and organic matter content significantly. Moreover. the decrease rate of 14 C-chlorsulfuron parent compound derived from 14 C-ER in soils followed the first order rate reaction, the half-life in Soil 1-Soil 7 were 13.0, 13.1, 17.7, 133.3, 21.8, 22.1, 33.2 days, respectively. It was concluded that soil pH was the main factor affecting the degradation of 14 C-chlorsulfuron. (2) The 14 C-BR content of 14 C-chlorsulfuron in soils increased sharply with the incubation time during the initial 20 days, then changed slowly with time. However, 14 C-BR content during the whole incubation depended on soil types. The order of 14 C-BR content followed Soil 1 > Soil 2, Soil 5 and Soil 6 > Soil 3 > Soil 7 > Soil 4. The maximum values of 14 C-BR content of 14 C-chlorsulfuron in Soil 1-Soil 7 were 53.3%, 40.9%, 37.8%, 16.4%, 42.5%, 41.0% and 31.3% of applied amount. In addition, the 14 C-BR content of 14 C-chlorsulfuron in soils was negatively related to soil pH significantly, and positively related to the clay content. The soil pH was found to be the main factor affecting BR formation of 14 C-chlorsulfuron among the basic properties of soil. (3) During the whole periods of the incubation, the 14 C-BR of 14 C-chlorsulfuron in soils was mainly distributed in fulvic acid and humin. The relative percent of 14 C-BR in fulvic acid was higher than in humin. While the relative percentage of the 14 C-BR in humic acid only account for 2%. It was suggested that fulvic acid played an important role

Effect of Simulated Acid Rain on Potential Carbon and Nitrogen Mineralization in Forest Soils

Institute of Scientific and Technical Information of China (English)

OUYANG Xue-Jun; ZHOU Guo-Yi; HUANG Zhong-Liang; LIU Ju-Xiu; ZHANG De-Qiang; LI Jiong

2008-01-01

Acid rain is a serious environmental problem worldwide. In this study, a pot experiment using forest soils planted with the seedlings of four woody species was performed with weekly treatments of pH 4.40, 4.00, 3.52, and 3.05 simulated acid rain (SAR) for 42 months compared to a control of pH 5.00 lake water. The cumulative amounts of C and N mineralization in the five treated soils were determined after incubation at 25 ℃ for 65 d to examine the effects of SAR treatments.For all five treatments, cumulative CO2-C production ranged from 20.24 to 27.81 mg kg-1 dry soil, net production of available N from 17.37 to 48.95 mg kg-1 dry soil, and net production of NO-3-N from 9.09 to 46.23 mg kg-1 dry soil. SAR treatments generally enhanced the emission of CO2-C from the soils; however, SAR with pH 3.05 inhibited the emission.SAR treatments decreased the net production of available N and NO3-N. The cumulative CH4 and N2O productions from the soils increased with increasing amount of simulated acid rain. The cumulative CO2-C production and the net production of available N of the soil under Acmena acuminatissima were significantly higher (P≤0.05) than those under Schima superba and Cryptocarya concinna. The mineralization of soil organic C was related to the contents of soil organic C and N, but was not related to soil pH. However, the overall effect of acid rain on the storage of soil organic matter and the cycling of important nutrients depended on the amount of acid deposition and the types of forests.

Carbon Mineralization Can Be Sustained or Even Stimulated under Fluctuating Redox Conditions in Tropical and Temperate Soils

Science.gov (United States)

Huang, W.; Hall, S. J.

2017-12-01

Soil carbon (C) mineralization is widely thought to be affected by O2 availability, and anaerobiosis represents a significant global mechanism of C stabilization. However, mineral-associated organic C (e.g. Fe-bound organic C) may be vulnerable to redox fluctuations due to release following Fe reduction, which could counteract protective effects of anaerobiosis. Many soils, including temperate Mollisols and tropical Oxisols, experience fluctuating redox conditions following moisture variations that could impact C cycling and stabilization. Here we incubated two soils with C4 leaf litter at different duration and frequencies of anaerobic periods for 128 days to investigate how redox fluctuations affect soil C mineralization. The treatments included static aerobic (control), and 2-, 4-, 8- and 12- day anaerobic followed by 4-day aerobic. We measured CO2, CH4, and their C isotope ratios. Longer durations of anaerobic conditions promoted greater Fe reduction and more DOC released. Notably, in both soils despite their large differences in composition, the production of CO2 and CH4 was stimulated under aerobic conditions following anaerobic conditions (relative to the control), which compensated for the decrease under anaerobic conditions. After 128 days, cumulative C mineralization in the control was similar between the Mollisol (9.7 mg C g-1) and the Oxisol (10.1 mg C g-1). The value in the Mollisol was significantly higher in the 12-day anaerobic treatment (11.2 mg C g-1) than the aerobic control and the 2-day anaerobic treatment (9.7 mg C g-1). In the Oxisol, cumulative C mineralization was not significantly affected by any of the fluctuating redox treatments relative to the control. Our findings challenge theory by showing that redox fluctuations can counteract the suppressive effects of O2 limitation on decomposition.

Collembolans feeding on soil affect carbon and nitrogen mineralization by their influence on microbial and nematode activities

Czech Academy of Sciences Publication Activity Database

Kaneda, Satoshi; Kaneko, N.

2008-01-01

Roč. 44, č. 3 (2008), s. 435-442 ISSN 0178-2762 Institutional research plan: CEZ:AV0Z60660521 Keywords : Collembola * mineral soil * nitrogen mineralization Subject RIV: EH - Ecology, Behaviour Impact factor: 1.446, year: 2008

Identification of a green rust mineral in a reductomorphic soil by Mossbauer and Raman spectroscopies

Science.gov (United States)

Trolard, F.; Génin, J.-M. R.; Abdelmoula, M.; Bourrié, G.; Humbert, B.; Herbillon, A.

1997-03-01

Mössbauer and Raman spectroscopies are used to identify for the first time a green rust as a mineral in a reductomorphic soil from samples extracted in the forest of Fougères (Brittany-France). The Mossbauer spectrum displays two characteristic ferrous and ferric quadrupole doublets, the abundance ratio Fe(II)/Fe(Ill) of which is close to 1. Comparison with synthetic mixed valence Fe(II)Fe(HI) hydroxides supports the conclusion that the most probable formula is Fe2(OH)5, i.e., according to the pyroaurite-like crystal structure [Fe(n1Fe1III)(OH),]+o [OH] -. The microprobe Raman spectrum exhibits two bands at 518 and 427 cm-' as for synthetic green rusts. When exposed to the air, the new mineral goes rapidly from bluish-green to ochrous. The formula is compatible with the values of ionic activity products Q for equilibria between aqueous iron species and minerals obtained from soil waters, which suggests that this new mineral is likely to control the mobility of Fe in the environment.

Surface materials map of Afghanistan: iron-bearing minerals and other materials

Science.gov (United States)

King, Trude V.V.; Kokaly, Raymond F.; Hoefen, Todd M.; Dudek, Kathleen B.; Livo, Keith E.

2012-01-01

This map shows the distribution of selected iron-bearing minerals and other materials derived from analysis of HyMap imaging spectrometer data of Afghanistan. Using a NASA (National Aeronautics and Space Administration) WB-57 aircraft flown at an altitude of ~15,240 meters or ~50,000 feet, 218 flight lines of data were collected over Afghanistan between August 22 and October 2, 2007. The HyMap data were converted to apparent surface reflectance, then further empirically adjusted using ground-based reflectance measurements. The reflectance spectrum of each pixel of HyMap data was compared to the spectral features of reference entries in a spectral library of minerals, vegetation, water, ice, and snow. This map shows the spatial distribution of iron-bearing minerals and other materials having diagnostic absorptions at visible and near-infrared wavelengths. These absorptions result from electronic processes in the minerals. Several criteria, including (1) the reliability of detection and discrimination of minerals using the HyMap spectrometer data, (2) the relative abundance of minerals, and (3) the importance of particular minerals to studies of Afghanistan's natural resources, guided the selection of entries in the reference spectral library and, therefore, guided the selection of mineral classes shown on this map. Minerals occurring abundantly at the surface and those having unique spectral features were easily detected and discriminated. Minerals having similar spectral features were less easily discriminated, especially where the minerals were not particularly abundant and (or) where vegetation cover reduced the absorption strength of mineral features. Complications in reflectance calibration also affected the detection and identification of minerals.

Effects of forest conversion on soil microbial communities depend on soil layer on the eastern Tibetan Plateau of China.

Directory of Open Access Journals (Sweden)

Ruoyang He

Full Text Available Forest land-use changes have long been suggested to profoundly affect soil microbial communities. However, how forest type conversion influences soil microbial properties remains unclear in Tibetan boreal forests. The aim of this study was to explore variations of soil microbial profiles in the surface organic layer and subsurface mineral soil among three contrasting forests (natural coniferous forest, NF; secondary birch forest, SF and spruce plantation, PT. Soil microbial biomass, activity and community structure of the two layers were investigated by chloroform fumigation, substrate respiration and phospholipid fatty acid analysis (PLFA, respectively. In the organic layer, both NF and SF exhibited higher soil nutrient levels (carbon, nitrogen and phosphorus, microbial biomass carbon and nitrogen, microbial respiration, PLFA contents as compared to PT. However, the measured parameters in the mineral soils often did not differ following forest type conversion. Irrespective of forest types, the microbial indexes generally were greater in the organic layer than in the mineral soil. PLFAs biomarkers were significantly correlated with soil substrate pools. Taken together, forest land-use change remarkably altered microbial community in the organic layer but often did not affect them in the mineral soil. The microbial responses to forest land-use change depend on soil layer, with organic horizons being more sensitive to forest conversion.

Organomineral Complexation at the Nanoscale: Iron Speciation and Soil Carbon Stabilization

Science.gov (United States)

Coward, E.; Thompson, A.; Plante, A. F.

2016-12-01

Much of the uncertainty in the biogeochemical behavior of soil carbon (C) in tropical ecosystems derives from an incomplete understanding of soil C stabilization processes. The 2:1 phyllosilicate clays often associated with temperate organomineral complexation are largely absent in tropical soils due to extensive weathering. In contrast, these soils contain an abundance of Fe- and Al-containing short-range-order (SRO) mineral phases capable of C stabilization through sorption or co-precipitation, largely enabled by high specific surface area (SSA). SRO-mediated organomineral associations may thus prove a critical, yet matrix-selective, driver of the long-term C stabilization capacity observed in tropical soils. Characterizing the interactions between inherently heterogeneous organic matter and amorphous mineralogy presses the limits of current analytical techniques. This work pairs inorganic selective dissolution with high-resolution assessment of Fe speciation to determine the contribution of extracted mineral phases to the mineral matrix, and to C stabilization capacity. Surface (0-20 cm) samples were taken from 20 quantitative soil pits within the Luquillo Critical Zone Observatory in northeast Puerto Rico stratified across granodioritic and volcaniclastic parent materials. 57Fe-Mössbauer spectroscopy (MBS) and x-ray diffraction (XRD) before and after Fe-SOM extraction were used to assess changes in the mineralogical matrix associated with SOM dissolution, while N2-BET sorption was used to determine the contributions of the extractable phases to SSA. Results indicate (1) selective extraction of soil C produces significant shifts in Fe phase distribution, (2) SRO minerals contribute substantially to SSA, and (3) SRO minerals appear protected by more crystalline phases via physical mechanisms, rather than dissolution-dependent chemical bonds. This nanoscale characterization of Fe-C complexes thus provides evidence for both anticipated mineral-organic and

Determination of hydrogen abundance in selected lunar soils

Science.gov (United States)

Bustin, Roberta

1987-01-01

Hydrogen was implanted in lunar soil through solar wind activity. In order to determine the feasibility of utilizing this solar wind hydrogen, it is necessary to know not only hydrogen abundances in bulk soils from a variety of locations but also the distribution of hydrogen within a given soil. Hydrogen distribution in bulk soils, grain size separates, mineral types, and core samples was investigated. Hydrogen was found in all samples studied. The amount varied considerably, depending on soil maturity, mineral types present, grain size distribution, and depth. Hydrogen implantation is definitely a surface phenomenon. However, as constructional particles are formed, previously exposed surfaces become embedded within particles, causing an enrichment of hydrogen in these species. In view of possibly extracting the hydrogen for use on the lunar surface, it is encouraging to know that hydrogen is present to a considerable depth and not only in the upper few millimeters. Based on these preliminary studies, extraction of solar wind hydrogen from lunar soil appears feasible, particulary if some kind of grain size separation is possible.

The global distribution and dynamics of surface soil moisture

Science.gov (United States)

McColl, Kaighin A.; Alemohammad, Seyed Hamed; Akbar, Ruzbeh; Konings, Alexandra G.; Yueh, Simon; Entekhabi, Dara

2017-01-01

Surface soil moisture has a direct impact on food security, human health and ecosystem function. It also plays a key role in the climate system, and the development and persistence of extreme weather events such as droughts, floods and heatwaves. However, sparse and uneven observations have made it difficult to quantify the global distribution and dynamics of surface soil moisture. Here we introduce a metric of soil moisture memory and use a full year of global observations from NASA's Soil Moisture Active Passive mission to show that surface soil moisture--a storage believed to make up less than 0.001% of the global freshwater budget by volume, and equivalent to an, on average, 8-mm thin layer of water covering all land surfaces--plays a significant role in the water cycle. Specifically, we find that surface soil moisture retains a median 14% of precipitation falling on land after three days. Furthermore, the retained fraction of the surface soil moisture storage after three days is highest over arid regions, and in regions where drainage to groundwater storage is lowest. We conclude that lower groundwater storage in these regions is due not only to lower precipitation, but also to the complex partitioning of the water cycle by the surface soil moisture storage layer at the land surface.

Heteroaggregation of graphene oxide with minerals in aqueous phase.

Science.gov (United States)

Zhao, Jian; Liu, Feifei; Wang, Zhenyu; Cao, Xuesong; Xing, Baoshan

2015-03-03

Upon release into waters, sediments, and soils, graphene oxide (GO) may interact with fine mineral particles. We investigated the heteroaggregation of GO with different minerals, including montmorillonite, kaolinite, and goethite, in aqueous phase. GO significantly enhanced the dispersion of positively charged goethite (>50%) via heteroaggregation, while there was no interaction between GO and negatively charged montmorillonite or kaolinite. Electrostatic attraction was the dominant force in the GO-goethite heteroaggregation (pH 4.0-8.5), and the dissolved Fe ions (formation of multilayered GO-goethite complex with high configurational stability. These findings are useful for understanding the interaction of GO with mineral surfaces, and potential fate and toxicity of GO under natural conditions in aquatic environments, as well as in soils and sediments.

Variations in the patterns of soil organic carbon mineralization and microbial communities in response to exogenous application of rice straw and calcium carbonate

Energy Technology Data Exchange (ETDEWEB)

Feng, Shuzhen [Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125 (China); University of Chinese Academy of Sciences, Beijing 100039 (China); Huanjiang Observation and Research Station for Karst Ecosystems, Chinese Academy of Sciences, Huangjiang 547100 (China); Huang, Yuan [Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125 (China); University of Chinese Academy of Sciences, Beijing 100039 (China); Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi 830011 (China); Ge, Yunhui [Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125 (China); College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128 (China); Su, Yirong [Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125 (China); Huanjiang Observation and Research Station for Karst Ecosystems, Chinese Academy of Sciences, Huangjiang 547100 (China); Xu, Xinwen; Wang, Yongdong [Xinjiang Institute of Ecology and Geography, Chinese Academy of Sciences, Urumqi 830011 (China); He, Xunyang, E-mail: hbhpjhn@isa.ac.cn [Key Laboratory of Agro-ecological Processes in Subtropical Region, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125 (China); Huanjiang Observation and Research Station for Karst Ecosystems, Chinese Academy of Sciences, Huangjiang 547100 (China)

2016-11-15

The addition of exogenous inorganic carbon (CaCO{sub 3}) and organic carbon has an important influence on soil organic carbon (SOC) mineralization in karst soil, but the microbial mechanisms underlying the SOC priming effect are poorly understood. We conducted a 100-day incubation experiment involving four treatments of the calcareous soil in southwestern China's karst region: control, {sup 14}C-labeled rice straw addition, {sup 14}C-labeled CaCO{sub 3} addition, and a combination of {sup 14}C-labeled rice straw and CaCO{sub 3}. Changes in soil microbial communities were characterized using denaturing gradient gel electrophoresis with polymerase chain reaction (PCR-DGGE) and real-time quantitative PCR (q-PCR). Both {sup 14}C-rice straw and Ca{sup 14}CO{sub 3} addition stimulated SOC mineralization, suggesting that organic and inorganic C affected SOC stability. Addition of straw alone had no significant effect on bacterial diversity; however, when the straw was added in combination with calcium carbonate, it had an inhibitory effect on bacterial and fungal diversity. At the beginning of the experimental period, exogenous additives increased bacterial abundance, although at the end of the 100-day incubation bacterial community abundance had gradually declined. Incubation time, exogenous input, and their interaction significantly affected SOC mineralization (in terms of priming and the cumulative amount of mineralization), microbial biomass carbon (MBC), and microbial community abundance and diversity. Moreover, the key factors influencing SOC mineralization were MBC, bacterial diversity, and soil pH. Overall, these findings support the view that inorganic C is involved in soil C turnover with the participation of soil microbial communities, promoting soil C cycling in the karst region. - Highlights: • Different patterns of {sup 14}C-rice straw and Ca{sup 14}CO{sub 3} addition on positive priming effects of SOC mineralization. • Inorganic C is involved in

Sorption behavior of bensulfuron-methyl on andisols and ultisols volcanic ash-derived soils: Contribution of humic fractions and mineral-organic complexes

Energy Technology Data Exchange (ETDEWEB)

Espinoza, Jeannette; Fuentes, Edwar [Department of Inorganic and Analytical Chemistry, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Olivos 1007, Casilla 233, Santiago (Chile); Baez, Maria E., E-mail: mbaez@ciq.uchile.c [Department of Inorganic and Analytical Chemistry, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Olivos 1007, Casilla 233, Santiago (Chile)

2009-12-15

Bensulfuron-methyl sorption was studied in Andisol and Ultisol soils in view of their characteristic physical and chemical properties, presenting acidic pH and variable charge. Humic and fulvic acids (HA and FA) and humin (HUM) contributions were established. Sorption was studied by using two synthetic sorbents, an aluminum-silicate with iron oxide coverage and the same sorbent coated with humic acid. Freundlich model described Bensulfuron-methyl behavior in all sorbents (R{sup 2} 0.969-0.998). K{sub f} for soils (8.3-20.7 mug{sup 1-1/n} mL{sup 1/n} g{sup -1}) were higher than those reported in the literature. Organic matter, halloysite or kaolinite, and specific surface area contributed to the global process. The highest K{sub f} for HA, FA and HUM were 539.5, 82.9, and 98.7 mug{sup 1-1/n} mL{sup 1/n} g{sup -1}. Model sorbents described the participation of variable charge materials with high adsorption capacity. The constant capacitance model was used to assess effects of Bensulfuron-methyl adsorption on the distribution of SOH, SOH{sub 2}{sup +} and SO{sup -} sites of sorbents. - Organic matter, phyllosilicates, variable charge minerals and organo-mineral complexes contribute to bensulfuron-methyl sorption on volcanic ash-derived soils.

Role of Arthropods in Maintaining Soil Fertility

Directory of Open Access Journals (Sweden)

Thomas W. Culliney

2013-09-01

Full Text Available In terms of species richness, arthropods may represent as much as 85% of the soil fauna. They comprise a large proportion of the meso- and macrofauna of the soil. Within the litter/soil system, five groups are chiefly represented: Isopoda, Myriapoda, Insecta, Acari, and Collembola, the latter two being by far the most abundant and diverse. Arthropods function on two of the three broad levels of organization of the soil food web: they are plant litter transformers or ecosystem engineers. Litter transformers fragment, or comminute, and humidify ingested plant debris, which is deposited in feces for further decomposition by micro-organisms, and foster the growth and dispersal of microbial populations. Large quantities of annual litter input may be processed (e.g., up to 60% by termites. The comminuted plant matter in feces presents an increased surface area to attack by micro-organisms, which, through the process of mineralization, convert its organic nutrients into simpler, inorganic compounds available to plants. Ecosystem engineers alter soil structure, mineral and organic matter composition, and hydrology. The burrowing by arthropods, particularly the subterranean network of tunnels and galleries that comprise termite and ant nests, improves soil porosity to provide adequate aeration and water-holding capacity below ground, facilitate root penetration, and prevent surface crusting and erosion of topsoil. Also, the movement of particles from lower horizons to the surface by ants and termites aids in mixing the organic and mineral fractions of the soil. The feces of arthropods are the basis for the formation of soil aggregates and humus, which physically stabilize the soil and increase its capacity to store nutrients.

Transformation of nitrogenous fertilizers of surface and deep application in calcareous soil

International Nuclear Information System (INIS)

Zuo Dongfeng

1990-01-01

The transformations of 15 N labelled fertilizer N in calcareous soil were studied under greennhouse conditions. The experimental results indicate that the ratio of fixed ammonium is closely related to the methods of fertilizer application to the soil. When fertilizer N applied as deep dressing the fixation of nitrogen by clay minerals and microorganisms may markedly reduce the losses of nitrogen, but the amount of nitrogen fixed by the clay minerals and that by microorganisms showed negative correlation (r = -0.9185 ** ). The more the amount of fixed nitrogen by clay minerals, the less by microorganisms. No obvious interrelation between the residual utilization of urea, ammonium bicarbonate, ammonium sulfate and the ammount of nitrogen fixed by organisms can be observed, but the residual utilization of these fertilizers by the succeeding crop has been related to the total amount of mineral nitrogen

Atrazine and its metabolites degradation in mineral salts medium and soil using an enrichment culture.

Science.gov (United States)

Kumar, Anup; Singh, Neera

2016-03-01

An atrazine-degrading enrichment culture was used to study degradation of atrazine metabolites viz. hydroxyatrazine, deethylatrazine, and deisopropylatrazine in mineral salts medium. Results suggested that the enrichment culture was able to degrade only hydroxyatrazine, and it was used as the sole source of carbon and nitrogen. Hydroxyatrazine degradation slowed down when sucrose and/or ammonium hydrogen phosphate were supplemented as the additional sources of carbon and nitrogen, respectively. The enrichment culture could degrade high concentrations of atrazine (up to 110 μg/mL) in mineral salts medium, and neutral pH was optimum for atrazine degradation. Further, except in an acidic soil, enrichment culture was able to degrade atrazine in three soil types having different physico-chemical properties. Raising the pH of acidic soil to neutral or alkaline enabled the enrichment culture to degrade atrazine suggesting that acidic pH inhibited atrazine-degrading ability. The study suggested that the enrichment culture can be successfully utilized to achieve complete degradation of atrazine and its persistent metabolite hydroxyatrazine in the contaminated soil and water.

Mars analog minerals' spectral reflectance characteristics under Martian surface conditions

Science.gov (United States)

Poitras, J. T.; Cloutis, E. A.; Salvatore, M. R.; Mertzman, S. A.; Applin, D. M.; Mann, P.

2018-05-01

We investigated the spectral reflectance properties of minerals under a simulated Martian environment. Twenty-eight different hydrated or hydroxylated phases of carbonates, sulfates, and silica minerals were selected based on past detection on Mars through spectral remote sensing data. Samples were ground and dry sieved to <45 μm grain size and characterized by XRD before and after 133 days inside a simulated Martian surface environment (pressure 5 Torr and CO2 fed). Reflectance spectra from 0.35 to 4 μm were taken periodically through a sapphire (0.35-2.5 μm) and zinc selenide (2.5-4 μm) window over a 133-day period. Mineral stability on the Martian surface was assessed through changes in spectral characteristics. Results indicate that the hydrated carbonates studied would be stable on the surface of Mars, only losing adsorbed H2O while maintaining their diagnostic spectral features. Sulfates were less stable, often with shifts in the band position of the SO, Fe, and OH absorption features. Silicas displayed spectral shifts related to SiOH and hydration state of the mineral surface, while diagnostic bands for quartz were stable. Previous detection of carbonate minerals based on 2.3-2.5 μm and 3.4-3.9 μm features appears to be consistent with our results. Sulfate mineral detection is more questionable since there can be shifts in band position related to SO4. The loss of the 0.43 μm Fe3+ band in many of the sulfates indicate that there are fewer potential candidates for Fe3+ sulfates to permanently exist on the Martian surface based on this band. The gypsum sample changed phase to basanite during desiccation as demonstrated by both reflectance and XRD. Silica on Mars has been detected using band depth ratio at 1.91 and 1.96 μm and band minimum position of the 1.4 μm feature, and the properties are also used to determine their age. This technique continues to be useful for positive silica identifications, however, silica age appears to be less consistent

Experimental study on soluble chemical transfer to surface runoff from soil.

Science.gov (United States)

Tong, Juxiu; Yang, Jinzhong; Hu, Bill X; Sun, Huaiwei

2016-10-01

Prevention of chemical transfer from soil to surface runoff, under condition of irrigation and subsurface drainage, would improve surface water quality. In this paper, a series of laboratory experiments were conducted to assess the effects of various soil and hydraulic factors on chemical transfer from soil to surface runoff. The factors include maximum depth of ponding water on soil surface, initial volumetric water content of soil, depth of soil with low porosity, type or texture of soil and condition of drainage. In the experiments, two soils, sand and loam, mixed with different quantities of soluble KCl were filled in the sandboxes and prepared under different initial saturated conditions. Simulated rainfall induced surface runoff are operated in the soils, and various ponding water depths on soil surface are simulated. Flow rates and KCl concentration of surface runoff are measured during the experiments. The following conclusions are made from the study results: (1) KCl concentration in surface runoff water would decrease with the increase of the maximum depth of ponding water on soil surface; (2) KCl concentration in surface runoff water would increase with the increase of initial volumetric water content in the soil; (3) smaller depth of soil with less porosity or deeper depth of soil with larger porosity leads to less KCl transfer to surface runoff; (4) the soil with finer texture, such as loam, could keep more fertilizer in soil, which will result in more KCl concentration in surface runoff; and (5) good subsurface drainage condition will increase the infiltration and drainage rates during rainfall event and will decrease KCl concentration in surface runoff. Therefore, it is necessary to reuse drained fertile water effectively during rainfall, without polluting groundwater. These study results should be considered in agriculture management to reduce soluble chemical transfer from soil to surface runoff for reducing non-point sources pollution.

Gross Nitrogen Mineralization in Surface Sediments of the Yangtze Estuary

Science.gov (United States)

Liu, Min; Li, Xiaofei; Yin, Guoyu; Zheng, Yanling; Deng, Fengyu

2016-01-01

Nitrogen mineralization is a key biogeochemical process transforming organic nitrogen to inorganic nitrogen in estuarine and coastal sediments. Although sedimentary nitrogen mineralization is an important internal driver for aquatic eutrophication, few studies have investigated sedimentary nitrogen mineralization in these environments. Sediment-slurry incubation experiments combined with 15N isotope dilution technique were conducted to quantify the potential rates of nitrogen mineralization in surface sediments of the Yangtze Estuary. The gross nitrogen mineralization (GNM) rates ranged from 0.02 to 5.13 mg N kg-1 d-1 in surface sediments of the study area. The GNM rates were generally higher in summer than in winter, and the relative high rates were detected mainly at sites near the north branch and frontal edge of this estuary. The spatial and temporal distributions of GNM rates were observed to depend largely on temperature, salinity, sedimentary organic carbon and nitrogen contents, and extracellular enzyme (urease and L-glutaminase) activities. The total mineralized nitrogen in the sediments of the Yangtze Estuary was estimated to be about 6.17 × 105 t N yr-1, and approximately 37% of it was retained in the estuary. Assuming the retained mineralized nitrogen is totally released from the sediments into the water column, which contributed 12–15% of total dissolved inorganic nitrogen (DIN) sources in this study area. This result indicated that the mineralization process is a significant internal nitrogen source for the overlying water of the Yangtze Estuary, and thus may contribute to the estuarine and coastal eutrophication. PMID:26991904