GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Biogeochemistry. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (206 pages)
    Edition: 1st ed.
    ISBN: 9783030959210
    Series Statement: Advances in Critical Zone Science Series
    DDC: 577.14
    Language: English
    Note: Intro -- Series Editor's Preface -- Contents -- 1 An Introduction to Biogeochemistry of the Critical Zone -- References -- 2 Hot Spots and Hot Moments in the Critical Zone: Identification of and Incorporation into Reactive Transport Models -- 2.1 Introduction -- 2.1.1 Definition of Terms -- 2.1.2 Scope and Overall Impact -- 2.2 Capturing Scales and Complexity Using Models -- 2.2.1 Hot Spots Within the Hyporheic Zone-The Redox Microzone Concept -- 2.2.2 HSHMs at the Floodplain Scale -- 2.2.3 HSHMs Along River Corridors -- 2.3 Current Understanding and the Path Forward -- 2.3.1 A Conceptual Take on HSHMs Using a Trait-Based Framework -- 2.3.2 Improvements in Field-Scale Characterization of Hyporheic Zones -- 2.3.3 Recent Developments in Observation and Modeling of Hot Spots Featuring the Sediment Water Interface -- 2.4 How Can Models Contribute? -- 2.4.1 Scale Aware Modeling/Parameterization -- 2.4.2 A Preemptive Prioritization of HSHMs -- 2.5 Concluding Remarks -- References -- 3 Constraints of Climate and Age on Soil Development in Hawai'i -- 3.1 Understanding Critical Zone Functioning Through State Factor Analysis -- 3.2 Physiographic Setting -- 3.3 Analytical Approach -- 3.4 Development of Critical Zone Properties Across the Hawaiian Islands -- 3.4.1 Weathering Depth and Chemical Denudation -- 3.4.2 Conditioning Lava Flows for Critical Zone Development -- 3.5 Biogeochemical Properties of Hawaiian Critical Zone -- 3.5.1 Weathering and Soil Properties -- 3.6 Soil Process Domains and Pedogenic Thresholds in Hawai'i -- 3.6.1 Process Domains -- 3.6.2 Transitions Among Process Domains -- 3.7 Conclusions -- References -- 4 Biofilms in the Critical Zone: Distribution and Mediation of Processes -- 4.1 Introduction -- 4.2 Documenting Environmental Biofilms Using the Scanning Electron Microscope -- 4.3 Biofilms in the Critical Zone. , 4.3.1 Plant Hosted, Biofilms Above Ground: Phyllosphere and Endosphere -- 4.3.2 Biofilms in the Soil -- 4.3.3 Biofilms in the Deep Critical Zone -- 4.4 Biofilm Mediation of Critical Zone Processes -- 4.4.1 Biofilm Role in OM Stabilization, Biogenic Minerals -- 4.4.2 Biofilm Role in Mineral Weathering -- 4.4.3 Biofilm Strategies to Survive Drought -- 4.5 Summary -- References -- 5 Eroded Critical Zone Carbon and Where to Find It: Examples from the IML-CZO -- 5.1 Introduction -- 5.1.1 Field Site -- 5.2 Methods -- 5.2.1 Estimates of Post-settlement Sediment Accumulation -- 5.2.2 Organic Carbon Concentrations and C-Isotopic Compositions -- 5.2.3 Biomarkers -- 5.3 Results and Discussion -- 5.3.1 Sediment and OC Inventories -- 5.3.2 Organic C Sources and Composition -- 5.4 Conclusions -- References -- 6 Advances in Biogeochemical Modeling for Intensively Managed Landscapes -- 6.1 Introduction -- 6.2 Long-Term Carbon Dynamics -- 6.3 Event-Scale Biogeochemical Dynamics: The Impact of Microtopography and Artificial Drainage -- 6.4 Root Zone Biogeochemistry -- References -- 7 Hillslope Position and Land-Use History Influence P Distribution in the Critical Zone -- 7.1 Introduction -- 7.1.1 Effect of Ecosystem Development on P Distribution -- 7.1.2 Effect of Topography on P Distribution -- 7.1.3 Effect of Land Use on P Distribution -- 7.1.4 Topography and Land Use in the Calhoun CZO -- 7.2 Methods -- 7.2.1 Study Site -- 7.2.2 Sample Collection -- 7.2.3 Sample Analyses -- 7.2.4 Data Analyses -- 7.3 Results -- 7.3.1 Soil Analyses -- 7.3.2 Soil Solution Analyses -- 7.3.3 Resin Capsule Analyses -- 7.3.4 Stream Analyses -- 7.4 Discussion -- 7.4.1 Hillslope Effects -- 7.4.2 Effects of Land Use on Vertical Leaching -- 7.4.3 Soil Solution P -- 7.4.4 Effects of Land-Use History on P Fractions -- 7.5 Conclusion -- References.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Global change biology 9 (2003), S. 0 
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Forest soils, rather than woody biomass, are the dominant long-term sink for N in forest fertilization studies and, by inference, for N from atmospheric deposition. Recent evidence of significant abiotic immobilization of inorganic-N in forest humus layers challenges a previously widely held view that microbial processes are the dominant pathways for N immobilization in soil. Understanding the plant, microbial, and abiotic mechanisms of N immobilization in forest soils has important implications for understanding current and future carbon budgets. Abiotic immobilization of nitrate is particularly perplexing because the thermodynamics of nitrate reduction in soils are not generally favorable under oxic conditions. Here we present preliminary evidence for a testable hypothesis that explains abiotic immobilization of nitrate in forest soils. Because iron (and perhaps manganese) plays a key role as a catalyst, with Fe(II) reducing nitrate and reduced forms of carbon then regenerating Fe(II), we call this ‘the ferrous wheel hypothesis’. After nitrate is reduced to nitrite, we hypothesize that nitrite reacts with dissolved organic matter through nitration and nitrosation of aromatic ring structures, thus producing dissolved organic nitrogen (DON). In addition to ignorance about mechanisms of DON production, little is known about DON dynamics in soil and its fate within ecosystems. Evidence from leaching and watershed studies suggests that DON production and consumption may be largely uncoupled from seasonal biological processes, although biological processes ultimately produce the DOC and reducing power that affect DON formation and the entire N cycle. The ferrous wheel hypothesis includes both biological and abiological processes, but the reducing power of plant-derived organic matter may build up over seasons and years while the abiotic reduction of nitrate and reaction of organic matter with nitrite may occur in a matter of seconds after nitrate enters the soil solution.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Soil Science Society of America journal 63 (1999), S. 169-177 
    ISSN: 1435-0661
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: + selectivity and (ii) structural charge as affected by pedogenic mineral transformations in an age sequence of Hawaiian soils. The Cs+→ Li+ exchange experiments were conducted on soils collected from six sites [basaltic parent material deposited 0.3, 20, 150, 400, 1400 and 4100 thousands of years (ky) ago.] Identical exchange experiments were performed with kaolinite, montmorillonite, and illite for comparison. Selectivity for Cs+ on soils and clays increased with adsorbed mole fraction of Cs+ . Cesium-accessible structural charge of the surface soils increased initially with soil age from 20 mmolc kg-1 at the 0.3 ky site to 113 mmolc kg-1 at the 400-ky site. Increased weathering beyond 400 ky reduced structural charge to 21 mmolc kg-1 for the oldest site. The magnitude of Cs retention in the soils is correlated with the presence of 2∝1 layer-type silicates detected by x-ray diffraction (XRD) after removal of poorly crystalline constituents. The results indicate a modest accumulation of secondary 2∝1 layer-type silicates (with larger accumulations of poorly crystalline clays), followed by their subsequent declines, during the course of soil weathering.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Soil Science Society of America journal 63 (1999), S. 850-857 
    ISSN: 1435-0661
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: a = 4.92) and background electrolyte (LiCl) onto specimen kaolinite was measured as a function of surface-bound humic acid (HA) concentration (f oc = 0-0.5%), pH (3-10), and ionic strength (1-10 mM). Complexation of HA on the kaolinite surface (4.5 mg C kg-1) reduced the point of zero net charge (pznc) for kaolinite by more than one pH unit and resulted in a significant increase in negative surface charge. Maximum sorption of quinoline occurred near its pKa for all sorbents. Below the pKa, quinoline sorption increases with increasing pH and decreasing proton competition. Above the pKa, sorption is reduced in parallel with (but offset to a higher pH from) the ionized fraction. Competition with Li+ for surface sites is apparent from diminished quinoline adsorption with increasing ionic strength, but sorption of the ionized form of quinoline over Li+ (Kexc = 65 at pH 5). However, increasing f oc diminishes quinoline sorption and selectivity (Kexc = 32 at pH 5) and increases sorption reversibility and selectivity for quinoline (Kexc = 4 at pH 5). The results indicate that mineral-sorbed humic substances can diminish retention of cationic quinoline despite an increase in overall cation-exchange capacity.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1573-515X
    Keywords: element fluxes ; prescribed burning ; soil solution chemistry ; throughfall ; water chemistry profiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Solution chemistry profiles of mixed-conifer forests in granitic catchments of the Sierra Nevada were measured for three years before (1987–1990) and three years after (1990–1993) prescribed fire. Wet deposition, throughfall and soil solution samplers were installed in both white-fir and giant-sequoia dominated forest stands underlain by poorly developed inceptisols. Stream water chemistry was monitored as part of an ongoing study of catchment outputs. Calcium, NO 3 − and Cl− were the major ions in precipitation. Canopy leaching increased mean concentrations of all major ions, especially K+ and Ca2+. Water flux through the soil occurred largely during spring snowmelt. Forest floor leachate represented the most concentrated solutions of major ions. Interaction with the mineral soil decreased mean concentrations of most species and the average composition of soil solutions closely resembled stream water at baseflow. Bicarbonate alkalinity, Ca2+, Mg2+, and Na+ were enriched in stream water relative to precipitation whereas inputs of H+, NH 4 + , NO 3 − and SO 4 2− were retained within the catchments. Burning of the forest understory and litter layer increased solute concentrations in soil solution and stream water. Mean soil solution Ca2+, Mg2+ and K+ concentrations increased more than 10 fold, but the relative predominance of these cations was not affected by burning. Sulfate concentration, which was very low in soil solutions of undisturbed stands (〈25 mmolc m−3), increased more than 100 times following fire. Ammonium concentration exhibited a rapid, short-term increase and then a decrease below pre-burn levels. Changes in soil solution chemistry were reflected in catchment outputs.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2011-11-01
    Description: Formation of faujasite- and sodalite/cancrinite-type phases associated with caustic waste reactions in the environment may structurally incorporate contaminant species such as radioactive Sr2+ and Cs+, and thus provide a mechanism of attenuation. To investigate mineral evolution and structural incorporation of cations in simplified experiments, aluminosilicate solids were precipitated homogeneously at room temperature from batch solutions containing a 1:1 molal ratio of Si to Al and 10-3 molal Sr and/or Cs, and aged for 30 or 548 days. Syntheses were done with solutions in equilibrium with atmospheric CO2 and with gas-purged solutions. Experimental products were characterized by bulk chemical analyses, chemical extractions, XRD, SEM/TEM, TGA, solid-state 27Al NMR, and Sr EXAFS. Chemical analysis showed that solids had a 1:1 Al:Si molar ratio, and that Sr was sequestered at higher amounts than Cs. After 30 days of aging in purged solutions, XRD showed that zeolite X (faujasite-type) was the only crystalline product. After aging 30 and 548 days in solutions equilibrated with atmospheric CO2, a mixture of sodalite, cancrinite, and minor zeolite X were produced. Surface areas of solids at 30 days were much lower than published values for zeolite phases synthesized at high temperature, although particle aging produced more crystalline and less aggregated phases with higher bulk surface areas. Characterization of products by 27Al NMR indicated only tetrahedrally coordinated Al. Measured isotropic shifts of primary resonances did not change substantially with precipitate aging although the primary mineral phase changed from zeolite X to sodalite/cancrinite, indicating local ordering of Al-Si tetrahedra. Analysis of reaction products by Sr EXAFS suggested Sr bonding in hexagonal prisms and six-membered rings of the supercages of zeolite X that may be more site specific than those of monovalent cations. For samples aged for 548 days, interatomic distances from Sr-EXAFS are consistent with partial Sr dehydration and bonding to framework oxygen atoms in sodalite cages or in large channels in cancrinite. Incorporation of Sr into both faujasite and sodalite/cancrinite phases is favored over Cs during room-temperature synthesis, possibly because of increased cation site competition between Cs+ and Na+. Results of this study help to constrain cation incorporation into sodalite/cancrinite mineral assemblages that form at caustic waste-impacted field sites and may aid in the predictive modeling of contaminant release.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...