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At least 55 records · Page 3Linked to original sources
USGS1999

Seasonal relationships between precipitation, forest floor, and streamwater nitrogen, Isle Royale, Michigan

The Upper Great Lakes receive large amounts of precipitation-NH + 4 and moderate NO - 3 inputs. Increased atmospheric inorganic N input has led to concern about ecosystem capacity to utilize excess N. This paper summarizes a 5-yr study of seasonal N content and flux in precipitation, snowpack, forest floor, and streamwater in order to assess the source of inorganic N outputs in streamflow from a small boreal watershed. Average precipitation N input was 3 kg ha -1 yr -1 . The peak snowpack N content averaged 0.55 kg ha -1 . The forest floor inorganic N pool was ≈ 2 kg ha -1 , eight times larger than monthly precipitation N input. The inorganic N pool size peaked in spring and early summer. Ninety percent of the forest floor inorganic N pool was made up of NH + 4 -N. Forest floor inorganic N pools generally increased with temperature. Net N mineralization was 15 kg ha -1 yr -1 , and monthly rates peaked in early summer. During winter, the mean monthly net N mineralization rate was twice the peak snowpack N content. Streamwater NO - 3 concentration peaked in winter, and inorganic N output peaked in late fall. Beneath the dominant boreal forest species, net N mineralization rates were positively correlated ( P < 0.05) with streamwater NO - 3 concentrations. Forest floor NO - 3 pools beneath alder [ Alnus rugosa (Du Roi) Spreng] were positively correlated ( P < 0.01) to streamwater NO - 3 output. At the watershed mouth, streamwater NO - 3 concentrations were positively correlated ( P < 0.05) with precipitation NO - 3 input and precipitation amount. The relatively small snowpack N content and seasonal precipitation N input compared to forest floor inorganic N pools and net N mineralization rates, the strong ecosystem retention of precipitation N inputs, and the seasonal streamwater NO - 3 concentration and output pattern all indicated that little streamwater NO - 3 came directly from precipitation or snowmelt.

Michigan↗
USGS1999

Importance of microscopy in durability studies of solidified and stabilized contaminated soils

Solidification/stabilization (S/S) is recognized by the U.S. EPA as a best demonstrated available technology for the containment of contaminated soils and other hazardous wastes that cannot be destroyed by chemical, thermal, or biological means. Despite the increased use of S/S technologies, little research has been conducted on the weathering and degradation of solidified and stabilized wastes once the treated materials have been buried. Published data to verify the performance and durability of landfilled treated wastes over time are rare. In this preliminary study, optical and electron microscopy (scanning electron microscopy [SEM], transmission electron microscopy [TEM] and electron probe microanalyses [EPMA]) were used to evaluate weathering features associated with metal-bearing contaminated soil that had been solidified and stabilized with Portland cement and subsequently buried on site, stored outdoors aboveground, or achieved in a laboratory warehouse for up to 6 yr. Physical and chemical alteration processes identified include: freeze-thaw cracking, cracking caused by the formation of expansive minerals such as ettringite, carbonation, and the movement of metals from waste aggregates into the cement micromass. Although the extent of degradation after 6 yr is considered slight to moderate, results of this study show that the same environmental concerns that affect the durability of concrete must be considered when evaluating the durability and permanence of the solidification and stabilization of contaminated soils with cement. In addition, such evaluations cannot be based on leaching and chemical analyses alone. The use of all levels of microscopic analyses must be incorporated into studies of the long-term performance of S/S technologies.Solidification/stabilization (S/S) is recognized by the U.S. EPA as a best demonstrated available technology for the containment of contaminated soils and other hazardous wastes that cannot be destroyed by chemical, thermal, or biological means. Despite the increased use of S/S technologies, little research has been conducted on the weathering and degradation of solidified and stabilized wastes once the treated materials have been buried. Published data to verify the performance and durability of landfilled treated wastes over time are rare. In this preliminary study, optical and electron microscopy (scanning electron microscopy [SEM], transmission electron microscopy [TEM] and electron probe microanalyses [EPMA]) were used to evaluate weathering features associated with metal-bearing contaminated soil that had been solidified and stabilized with Portland cement and subsequently buried on site, stored outdoors aboveground, or archived in a laboratory, warehouse for up to 6 yr. Physical and chemical alteration processes identified include: freeze-thaw cracking, cracking caused by the formation of expansive minerals such as ettringite, carbonation, and the movement of metals from waste aggregates into the cement micromass. Although the extent of degradation after 6 yr is considered slight to moderate, results of this study show that the same environmental concerns that affect the durability of concrete must be considered when evaluating the durability and permanence of the solidification and stabilization of contaminated soils with cement. In addition, such evaluations cannot be based on leaching and chemical analyses alone. The use of all levels of microscopic analyses must be incorporated into studies of the long-term performance of S/S technologies.

Soil Science Society of America Journal↗
USGS2000

Nitrite fixation by humic substances: Nitrogen-15 nuclear magnetic resonance evidence for potential intermediates in chemodenitrification

Studies have suggested that NO − 2 , produced during nitrification and denitrification, can become incorporated into soil organic matter and, in one of the processes associated with chemodenitrification, react with organic matter to form trace N gases, including N 2 O. To gain an understanding of the nitrosation chemistry on a molecular level, soil and aquatic humic substances were reacted with 15 N-labeled NaNO 2 , and analyzed by liquid phase 15 N and 13 C nuclear magnetic resonance (NMR). The International Humic Substances Society (IHSS) Pahokee peat and peat humic acid were also reacted with Na 15 NO 2 and analyzed by solid-state 15 N NMR. In Suwannee River, Armadale, and Laurentian fulvic acids, phenolic rings and activated methylene groups underwent nitrosation to form nitrosophenols (quinone monoximes) and ketoximes, respectively. The oximes underwent Beckmann rearrangements to 2° amides, and Beckmann fragmentations to nitriles. The nitriles in turn underwent hydrolysis to 1° amides. Peaks tentatively identified as imine, indophenol, or azoxybenzene nitrogens were clearly present in spectra of samples nitrosated at pH 6 but diminished at pH 3. The 15 N NMR spectrum of the peat humic acid exhibited peaks corresponding with N-nitroso groups in addition to nitrosophenols, ketoximes, and secondary Beckmann reaction products. Formation of N-nitroso groups was more significant in the whole peat compared with the peat humic acid. Carbon-13 NMR analyses also indicated the occurrence of nitrosative demethoxylation in peat and soil humic acids. Reaction of 15 N-NH 3 fixated fulvic acid with unlabeled NO − 2 resulted in nitrosative deamination of aminohydroquinone N, suggesting a previously unrecognized pathway for production of N 2 gas in soils fertilized with NH 3

Soil Science Society of America Journal↗
USGS2000

Recharge from a subsidence crater at the Nevada test site

Current recharge through the alluvial fans of the Nevada Test Site (NTS) is considered to be negligible, but the impact of more than 400 nuclear subsidence craters on recharge is uncertain. Many of the craters contain a playa region, but the impact of these playas has not been addressed. It was hypothesized that a crater playa would focus infiltration through the surrounding coarser-grained material, thereby increasing recharge. Crater U5a was selected because it represented a worst case for runoff into craters. A borehole was instrumented for neutron logging beneath the playa center and immediately outside the crater. Physical and hydraulic properties were measured along a transect in the crater and outside the crater. Particle-size analysis of the 14.6 m of sediment in the crater and morphological features of the crater suggest that a large ponding event of &asymp;63000 m 3 had occurred since crater formation. Water flow simulations with HYDRUS-2D, which were corroborated by the measured water contents, suggest that the wetting front advanced initially by as much as 30 m yr &minus;1 with a recharge rate 32 yr after the event of 2.5 m yr &minus;1 Simulations based on the measured properties of the sediments suggest that infiltration will occur preferentially around the playa perimeter. However, these sediments were shown to effectively restrict future recharge by storing water until removal by evapotranspiration (ET). This work demonstrated that subsidence craters may be self-healing.

Soil Science Society of America Journal↗
USGS2000

Forest soil chemistry and terrain attributes in a Catskills watershed

Knowledge of soil chemistry is useful in assessing the sensitivity of forested areas to natural and anthropogenic disturbances, but characterizing large areas is expensive because of the large sample numbers required and the cost of soil chemical analyses. We collected and chemically analyzed soil samples from 72 sites within a 214-ha watershed in the Catskill Mountains of New York to evaluate factors that influence soil chemistry and whether terrain features could be used to predict soil chemical properties. Using geographic information system (GIS) techniques, we determined five terrain attributes at each sampling location: (i) slope, (ii) aspect, (iii) elevation, (iv) topographic index, and (v) flow accumulation. These attributes were ineffective in predicting the chemical properties of organic and mineral soil samples; together they explained only 4 to 25% of the variance in pH(w), effective cation-exchange capacity (CEC(e)), exchangeable bases, exchangeable acidity, total C, total N, and C/N ratio. Regressions among soil properties were much better; total C and pH(w) together explained 33 to 66% of the variation in exchangeable bases and CEC(e). Total C was positively correlated with N (r = 0.91 and 0.96 in Oa horizons and mineral soil, respectively), exchangeable bases (r = 0.65, 0.76), and CEC(e) (r = 0.54, 0.44), indicating the importance of organic matter to the chemistry of these acidic soils. The fraction of CEC(e) occupied by H explained 44% of the variation in pH(w). Soil chemical properties at this site vary on spatial scales finer than typical GIS analyses, resulting in relationships with poor predictive power. Thus, interrelationships among soil properties are more reliable for prediction.Knowledge of soil chemistry is useful in assessing the sensitivity of forested areas to natural and anthropogenic disturbances, but characterizing large areas is expensive because of the large sample numbers required and the cost of soil chemical analyses. We collected and chemically analyzed soil samples from 72 sites within a 214-ha watershed in the Catskill Mountains of New York to evaluate factors that influence soil chemistry and whether terrain features could be used to predict soil chemical properties. Using geographic information system (GIS) techniques, we determined five terrain attributes at each sampling location: (i) slope, (ii) aspect, (iii) elevation, (iv) topographic index, and (v) flow accumulation. These attributes were ineffective in predicting the chemical properties of organic and mineral soil samples; together they explained only 4 to 25% of the variance in pHw, effective cation-exchange capacity (CECe), exchangeable bases, exchangeable acidity, total C, total N, and C/N ratio. Regressions among soil properties were much better; total C and pHw together explained 33 to 66% of the variation in exchangeable bases and CECe. Total C was positively correlated with N (r = 0.91 and 0.96 in Oa horizons and mineral soil, respectively), exchangeable bases (r = 0.65, 0.76), and CECe (r = 0.54, 0.44), indicating the importance of organic matter to the chemistry of these acidic soils. The fraction of CECe occupied by H explained 44% of the variation in pHw. Soil chemical properties at this site vary on spatial scales finer than typical GIS analyses, resulting in relationships with poor predictive power. Thus, interrelationships among soil properties are more reliable for prediction.

New York↗
USGS2000

Carbon distribution in subalpine forests and meadows of the Olympic Mountains, Washington

stimates of C storage in mountainous regions are rare. Forest–meadow ecotones in subalpine ecosystems, which contain a mosaic of forests and meadows, may be particularly sensitive to future changes in climate and are therefore important to include in estimates of terrestrial C storage. In this study, we quantified soil C and ecosystem C pools in subalpine forest and meadow soils of the northeastern (NE, dry climate) and southwestern (SW, wet climate) Olympic Mountains. Carbon concentrations of mineral soil are relatively high in upper horizons, ranging from 43 to 142 g kg −1 in NE soils and 27 to 162 g kg −1 in SW soils. Northeastern meadow soils store more C than NE forests ( P = 0.009) , while SW forest soils store more C than SW meadows ( P = 0.038) Ecosystem C storage is greater in forests than in meadows. Under a warmer climatic scenario with drier summers and wetter winters, subalpine C storage may decrease in the NE and increase in the SW, and changes in C storage will be closely related to vegetation distribution, ecosystem productivity, decomposition rates, and local disturbance regimes. Because ecosystem processes and associated C storage differ between high- and low-elevation ecosystems, it is important that data from both high- and low-elevation sites are included in estimates of C storage in terrestrial ecosystems.

Soil Science Society of America Journal↗
USGS2000

Calcium depletion in a Southeastern United States forest ecosystem

Forest soil Ca depletion through leaching and vegetation uptake may threaten long-term sustainability of forest productivity in the southeastern USA. This study was conducted to assess Ca pools and fluxes in a representative southern Piedmont forest to determine the soil Ca depletion rate. Soil Ca storage, Ca inputs in atmospheric deposition, and outputs in soil leaching and vegetation uptake were investigated at the Panola Mountain Research Watershed (PMRW) near Atlanta, GA. Average annual outputs of 12.3 kg ha −1 yr −1 in uptake into merchantable wood and 2.71 kg ha −1 yr −1 soil leaching exceeded inputs in atmospheric deposition of 2.24 kg ha −1 yr −1 The annual rate of Ca uptake into merchantable wood exceeds soil leaching losses by a factor of more than five. The potential for primary mineral weathering to provide a substantial amount of Ca inputs is low. Estimates of Ca replenishment through mineral weathering in the surface 1 m of soil and saprolite was estimated to be 0.12 kg ha −1 yr −1 The weathering rate in saprolite and partially weathered bedrock below the surface 1 m is similarly quite low because mineral Ca is largely depleted. The soil Ca depletion rate at PMRW is estimated to be 12.7 kg ha −1 yr −1 At PMRW and similar hardwood-dominated forests in the Piedmont physiographic province, Ca depletion will probably reduce soil reserves to less than the requirement for a merchantable forest stand in ≈80 yr. This assessment and comparable analyses at other southeastern USA forest sites suggests that there is a strong potential for a regional problem in forest nutrition in the long term.

Soil Science Society of America Journal↗
USGS2001

Impact of climate and parent material on chemical weathering in Loess-derived soils of the Mississippi River valley

Peoria Loess-derived soils on uplands east of the Mississippi River valley were studied from Louisiana to Iowa, along a south-to-north gradient of decreasing precipitation and temperature. Major element analyses of deep loess in Mississippi and Illinois show that the composition of the parent material is similar in the northern and southern parts of the valley. We hypothesized that in the warmer, wetter parts of the transect, mineral weathering should be greater than in the cooler, drier parts of the transect. Profile average values of CaO/TiO 2 , MgO/TiO 2 , K 2 O/TiO 2 and Na 2 O/TiO 2 , Sr/Zr, Ba/Zr, and Rb/Zr represent proxies for depletion of loess minerals such as calcite, dolomite, hornblende, mica, and plagioclase. All ratios show increases from south to north, supporting the hypothesis of greater chemical weathering in the southern part of the valley. An unexpected result is that profile average values of Al 2 O 3 /TiO 2 and Fe 2 O 3 /TiO 2 (proxies for the relative abundance of clay minerals) show increases from south to north. This finding, while contrary to the evidence of greater chemical weathering in the southern part of the transect, is consistent with an earlier study which showed higher clay contents in Bt horizons of loess-derived soils in the northern part of the transect. We hypothesize that soils in the northern part of the valley received fine-grained loess from sources to the west of the Mississippi River valley either late in the last glacial period, during the Holocene or both. In contrast, soils in the southern part of the valley were unaffected by such additions.

Arkansas, Illinois, Iowa, Kentucky, Louisiana, Mis↗
USGS2002

Calibration and temperature correction of heat dissipation matric potential sensors

This paper describes how heat dissipation sensors, used to measure soil water matric potential, were analyzed to develop a normalized calibration equation and a temperature correction method. Inference of soil matric potential depends on a correlation between the variable thermal conductance of the sensor's porous ceramic and matric potential. Although this correlation varies among sensors, we demonstrate a normalizing procedure that produces a single calibration relationship. Using sensors from three sources and different calibration methods, the normalized calibration resulted in a mean absolute error of 23% over a matric potential range of −0.01 to −35 MPa. Because the thermal conductivity of variably saturated porous media is temperature dependent, a temperature correction is required for application of heat dissipation sensors in field soils. A temperature correction procedure is outlined that reduces temperature dependent errors by 10 times, which reduces the matric potential measurement errors by more than 30%. The temperature dependence is well described by a thermal conductivity model that allows for the correction of measurements at any temperature to measurements at the calibration temperature.

Soil Science Society of America Journal↗
USGS2003

Formation and loss of humic substances during decomposition in a pine forest floor

Since twice as much C is sequestered in soils as is contained in the atmosphere, the factors controlling the decomposition rate of soil C are important to the assessment of the effects of climatic change. The formation of chemically resistant humic substances might be an important process controlling recycling of CO 2 to the atmosphere. Our objectives were to measure the rate of formation and loss of humic substances during 13 yr of litter decomposition . We placed nets on the floor of a white pine (Pinus strobus) forest to separate each annual layer of litter for 13 yr and measured humic substance concentration using NaOH extraction followed by chromatographic fractionation. The humic acid fraction increased from 2.1% of the C in litterfall to 15.7% after 1 yr. On a grams per square meter (g m -2 ) basis the humic substance fraction increased during the first year and then declined, with a half decay time (t 1/2 ) of 5.1 yr, which was significantly slower than the bulk litter (t 1/2 = 3.9 yr). The carboxylic C concentration estimated from 13 C nuclear magnetic resonance (NMR) increased in the litter over time, though total mass of carboxylic acid C in the forest floor also declined over the 13-yr period (t 1/2 = 4.6 yr). While humic substances in the forest floor decomposed at a somewhat slower rate than bulk litter during Years 1 to 13, they decomposed much faster than has been calculated from 14 C dating of the refractory fraction of organic matter in the mineral soil.

Soil Science Society of America Journal↗
USGS2003

Hydric soils in a southeastern Oregon vernal pool

Vernal pools on the High Lava Plain of the northern Great Basin become ponded in most years, but their soils exhibit weak redoximorphic features indicative of hydric conditions. We studied the hydrology, temperature, redox potentials, soil chemistry, and soil morphology of a vernal pool to determine if the soils are hydric, and to evaluate hydric soil field indicators. We collected data for 3 yr from piezometers, Pt electrodes, and thermocouples. Soil and water samples were analyzed for pH, organic C, and extractable Fe and Mn. Soils were ponded from January through April or May, but subsurface saturation was never detected. Soil temperatures 50 cm below the surface rose above 5°C by March. Clayey Bt horizons perched water and limited saturation to the upper 10 cm. Redox potentials at a 5-cm depth were often between 200 and 300 mV, indicating anaerobic conditions, but producing soluble Fe 2+ concentrations <1 mg L −1 Extractable soil Fe contents indicated Fe depletion from pool surface horizons and accumulation at or near the upper Bt1 horizon. Depletions and concentrations did not satisfy the criteria of any current hydric soil indicators. We recommend development of new indicators based on acceptance of fewer, less distinct redox concentrations for recognition of a depleted A horizon, and on presence of a thin zone containing redox concentrations located in the upper part of the near-surface perching horizon.

Soil Science Society of America Journal↗
USGS2005

Phosphate reactivity in long-term poultry litter-amended southern Delaware sandy soils

Eutrophication caused by dissolved P from poultry litter (PL)-amended agricultural soils has been a serious environmental concern in the Delaware-Maryland-Virginia Peninsula (Delmarva), USA. To evaluate state and federal nutrient management strategies for reducing the environmental impact of soluble P from long-term PL-amended Delaware (DE) soils, we investigated (i) inorganic P speciation; (ii) P adsorption capacity; and (iii) the extent of P desorption. Although the electron microprobe (EMP) analyses showed a strong correlation between P and Al/Fe, crystalline Al/Fe-P precipitates were not detected by x-ray diffraction (XRD). Instead, the inorganic P fractionation analyses showed high levels of oxalate extractable P, Al, and Fe fractions (615-858, 1215-1478, and 337-752 mg kg-1, respectively), which were susceptible to slow release during the long-term (30-d) P desorption experiments at a moderately acidic soil pHwater. The labile P in the short-term (24-h) desorption studies was significantly associated with oxalate and F extractable Fe and Al, respectively. This was evident in an 80% reduction maximum in total desorbable P from NH4 oxalate/F pretreated soils. In the adsorption experiments, P was strongly retained in soils at near targeted pH of lime (???6.0), but P adsorption gradually decreased with decreasing pH near the soil pHwater (???5.0). The overall findings suggest that P losses from the can be suppressed by an increase in the P retention capacity of soils via (i) an increase in the number of lime applications to maintain soil pHwater at near targeted pH values, and/or (ii) alum/iron sulfate amendments to provide additional Al- and Fe-based adsorbents. ?? Soil Science Society of America.

Soil Science Society of America Journal↗
USGS2004

Pedogenic silica accumulation in chronosequence soils, southern California

Chronosequential analysis of soil properties has proven to be a valuable approach for estimating ages of geomorphic surfaces where no independent age control exists. In this study we examined pedogenic silica as an indicator of relative ages of soils and geomorphic surfaces, and assessed potential sources of the silica. Pedogenic opaline silica was quantified by tiron (4,5-dihydroxy-1,3-benzene-disulfonic acid [disodium salt], C 6 H 4 Na 2 O 8 S 2 ) extraction for pedons in two different chronosequences in southern California, one in the San Timoteo Badlands and one in Cajon Pass. The soils of both of these chronosequences are developed in arkosic sediments and span 11.5 to 500 ka. The amount of pedogenic silica increases with increasing duration of pedogenesis, and the depth of the maximum silica accumulation generally coincides with the maximum expression of the argillic horizon. Pedogenic silica has accumulated in all of the soils, ranging from 1.2% tiron-extractable Si (Si tn ) in the youngest soil to 4.6% in the oldest. Primary Si decreases with increasing duration of weathering, particularly in the upper horizons, where weathering conditions are most intense. The loss of Si coincides with the loss of Na and K, implicating the weathering of feldspars as the likely source of Si loss. The quantity of Si lost in the upper horizons is adequate to account for the pedogenic silica accumulation in the subsoil. Pedogenic silica was equally effective as pedogenic Fe oxides as an indicator of relative soil age in these soils.

California↗
USGSDate not supplied

Characterizing the two-dimensional thermal conductivity distribution in a sand and gravel aquifer

Both hydrologic and thermal transport properties play a significant role in the movement of heat through permeable sedimentary material; however, the thermal conductivity is rarely characterized in detailed spatial resolution. As part of a study of the movement of thermal plumes through a sand and gravel aquifer, we have constructed a two-dimensional profile of thermal conductivity. This work consisted of: (i) measuring the thermal conductivity of the soil solids, λ s , for the main stratigraphic units using the steady-state divided-bar apparatus and estimating conductivity from mineral composition; (ii) measuring the volumetric water content and porosity using crosshole ground-penetrating radar; (iii) evaluating four models used to predict the apparent thermal conductivity, λ, of variably saturated soils and selecting the best model using the information-theoretic approach, (iv) calculating the λ field on a 0.25-m square cell grid using measured data and the selected model, and (v) simulating thermal transport within the two-dimensional domain using a finite element numerical model. The apparent thermal conductivity in the saturated aquifer ranges from 2.14 to 2.69 W m −1 K −1 with a mean of 2.42 W m −1 K −1 Numerical simulations show that the heterogeneous thermal conductivity field results in increased thermal dispersion that is most pronounced at the plume front. Our values for λ and λ s may be used for glacial soils with similar mineralogy and texture. Our methods may also be used at other sites to construct the thermal conductivity distribution.

Ontario↗
USGS2005

The soil physics contributions of Edgar Buckingham

During 1902 to 1906 as a soil physicist at the USDA Bureau of Soils (BOS), Edgar Buckingham originated the concepts of matric potential, soil–water retention curves, specific water capacity, and unsaturated hydraulic conductivity ( K ) as a distinct property of a soil. He applied a formula equivalent to Darcy's law (though without specific mention of Darcy's work) to unsaturated flow. He also contributed significant research on quasi-empirical formulas for K as a function of water content, water flow in capillary crevices and in thin films, and scaling. Buckingham's work on gas flow in soils produced paradigms that are consistent with our current understanding. His work on evaporation elucidated the concept of self-mulching and produced sound and sometimes paradoxical generalizations concerning conditions that favor or retard evaporation. Largely overshadowing those achievements, however, is that he launched a theory, still accepted today, that could predict transient water content as a function of time and space. Recently discovered documents reveal some of the arguments Buckingham had with BOS officials, including the text of a two-paragraph conclusion of his famous 1907 report on soil water, and the official letter documenting rejection of that text. Strained interpersonal relations motivated the departure of Buckingham and other brilliant physicists (N.E. Dorsey, F.H. King, and Lyman Briggs) from the BOS during 1903 to 1906. Given that Buckingham and his BOS colleagues had been rapidly developing the means of quantifying unsaturated flow, these strained relations probably slowed the advancement of unsaturated flow theory.

Soil Science Society of America Journal↗
USGS2010

Soil organic carbon stocks in Alaska estimated with spatial and pedon data

Temperatures in high-latitude ecosystems are increasing faster than the average rate of global warming, which may lead to a positive feedback for climate change by increasing the respiration rates of soil organic C. If a positive feedback is confirmed, soil C will represent a source of greenhouse gases that is not currently considered in international protocols to regulate C emissions. We present new estimates of the stocks of soil organic C in Alaska, calculated by linking spatial and field data developed by the USDA NRCS. The spatial data are from the State Soil Geographic database (STATSGO), and the field and laboratory data are from the National Soil Characterization Database, also known as the pedon database. The new estimates range from 32 to 53 Pg of soil organic C for Alaska, formed by linking the spatial and field data using the attributes of Soil Taxonomy. For modelers, we recommend an estimation method based on taxonomic subgroups with interpolation for missing areas, which yields an estimate of 48 Pg. This is a substantial increase over a magnitude of 13 Pg estimated from only the STATSGO data as originally distributed in 1994, but the increase reflects different estimation methods and is not a measure of the change in C on the landscape. Pedon samples were collected between 1952 and 2002, so the results do not represent a single point in time. The linked databases provide an improved basis for modeling the impacts of climate change on net ecosystem exchange.

Soil Science Society of America Journal↗
USGS2010

Erosion and vegetation restoration impacts on ecosystem carbon dynamics in South China

To quantify the consequences of erosion and vegetation restoration on ecosystem C dynamics (a key element in understanding the terrestrial C cycle), field measurements were collected since 1959 at two experimental sites set up on highly disturbed barren land in South China. One site had received vegetation restoration (the restored site) while the other received no planting and remained barren (the barren site). The Erosion-Deposition Carbon Model (EDCM) was used to simulate the ecosystem C dynamics at both sites. The on-site observations in 2007 showed that soil organic C (SOC) storage in the top 80-cm soil layer at the barren site was 50.3 ± 3.5 Mg C ha −1 , half that of the restored site. The SOC and surface soil loss by erosion at the restored site from 1959 to 2007 was 3.7 Mg C ha −1 and 2.2 cm, respectively—one-third and one-eighth that of the barren site. The on-site C sequestration in SOC and vegetation at the restored site was 0.67 and 2.5 Mg C ha −1 yr −1 , respectively, from 1959 to 2007, driven largely by tree growth and high atmospheric N deposition in the study area. Simulated findings suggested that higher N deposition resulted in higher on-site SOC storage in the soil profile (with SOC in the top 20-cm layer increasing more significantly), and higher on-site ecosystem C sequestration as long as N saturation was not reached. Lacking human-induced vegetation recovery, the barren site remained as barren land from 1959 to 2007 and the on-site C decrease was 0.28 Mg C ha −1 yr −1 Our study clearly indicated that vegetation restoration and burial by soil erosion provide a large potential C sink in terrestrial ecosystems.

Soil Science Society of America Journal↗
USGS2010

Biologic origin of iron nodules in a marine terrace chronosequence, Santa Cruz, California

The distribution, chemistry, and morphology of Fe nodules were studied in a marine terrace soil chronosequence northwest of Santa Cruz, California. The Fe nodules are found at depths <1 m on all terraces. The nodules consisted of soil mineral grains cemented by Fe oxides. The nodules varied in size from 0.5 to 25 mm in diameter. Nodules did not occur in the underlying regolith. The Fe-oxide mineralogy of the nodules was typically goethite; however, a subset of nodules consisted of maghemite. There was a slight transformation to hematite with time. The abundance of soil Fe nodules increased with terrace age on the five terraces studied (aged 65,000-226,000 yr). Scanning electron microscopy (SEM) revealed Fe-oxide-containing fungal hyphae throughout the nodules, including organic structures incorporating fine-grained Fe oxides. The fine-grained nature of the Fe oxides was substantiated by M??ssbauer spectroscopy. Our microscopic observations led to the hypothesis that the nodules in the Santa Cruz terrace soils are precipitated by fungi, perhaps as a strategy to sequester primary mineral grains for nutrient extraction. The fungal structures are fixed by the seasonal wetting and dry cycles and rounded through bioturbation. The organic structures are compacted by the degradation of fungal C with time. ?? Soil Science Society of America. All rights reserved.

Soil Science Society of America Journal↗