Black carbon estimation in French calcareous soils using chemo‐thermal oxidation method

We studied the black carbon (BC) content of ca. 405 samples from French topsoil and artificial soil and carbonate mixtures. Our protocol involved three main steps: (i) decarbonation by HCl, (ii) elimination of non‐pyrogenic organic carbon in a furnace at 375 °C, and (iii) quantification of residual carbon by CHN analysis. BC content increased for calcareous soils according to their carbonates content. Subsequent analyses confirmed the existence of a methodological artefact for BC determination only in calcareous soils. Decarbonation changes the thermal properties of organic matter, creating more recalcitrant carbon than in the initial sample. Higher CaCO₃ and organic carbon content results in a more pronounced artefact. The reversal of the first two steps of the chemo‐thermal oxidation method (i.e. thermal oxidation before soil decarbonation) eliminates this artefact. Overall, our results suggest that BC content may have been overestimated in a large number of studies on calcareous soils.     

Accurate and Precise Measurement of Organic Carbon Content in Carbonate-Rich Soils

Accurate measurement of soil organic carbon (SOC) is dependent on precise and fast methods for the separation of organic and inorganic carbon. The widely used methods involving thermal decomposition of soil samples at a specific temperature in an automated carbon (C) analyzer are susceptible to interference by carbonates and overestimation of organic C, and thus removal of carbonates by acid pretreatment of samples is recommended. Two carbonate-removal pretreatments including hydrochloric (HCl) acid addition and HCl fumigation are compared using the calcium carbonate (CaCO₃) standard and soil samples of varying SOC contents. Both pretreatment methods provided similar measurements of organic C, indicating that both methods are efficient in removal of carbonates present in the soil. However, the HCl fumigation method exhibited greater accuracy and precision compared to the HCl addition method. Hence, SOC measurement procedure involving HCl fumigation as a pretreatment for the removal of carbonates is recommended for carbonate-rich soils.     

Direct Determination of Organic Carbon by Dry Combustion in Soils with Carbonates

Abstract

In acid soils, where organic carbon (C) corresponds to total C, direct determination of organic C by dry combustion is possible, whereas in soils with carbonates also a separate measurement of inorganic C is required. In this case, direct quantification of organic C can be accomplished by the Walkley‐Black method, which is time‐consuming and involves greatly polluting by‐products. Hence, a method able to determine directly organic C by dry combustion is strongly needed for soils with carbonates. This study proposes such a method, after it was found to be highly reliable in calcareous soils of a Mediterranean island. The correction factor to use in the Walkley‐Black method to account for nonrecoverable C was calculated. It does not show any overall relationship with the contents of either organic C or inorganic C, and for all land uses examined in the island, it is not significantly different from the commonly suggested value 1.30.     

Carbon and nitrogen mineralization in acidic, limed and calcareous agricultural soils: Apparent and actual effects

Soil pH and calcium carbonate contents are often hypothesized to be important factors controlling organic matter turnover in agricultural soils. The aim of this study was to differentiate the effects of soil pH from those related to carbonate equilibrium on C and N dynamics. The relative contributions of organic and inorganic carbon in the CO₂ produced during laboratory incubations were assessed. Five agricultural soils were compared: calcareous (74% CaCO₃), loess (0.2% CaCO₃) and an acidic soil which had received different rates of lime 20 years ago (0, 18 or 50 t ha⁻¹). Soil aggregates were incubated with or without rape residues under aerobic conditions for 91 days at 15 °C. The C and N mineralized, soil pH, O₂ consumption and respiratory quotient (RQ=ΔCO₂/ΔO₂) were monitored, as well as the δ¹³C composition of the evolved CO₂ to determine its origin (mineral or organic). Results showed that in non-amended soils, the cumulative CO₂ produced was significantly greater in the limed soil with a pH>7 than in the same soil with less or no lime added, whereas there was no difference in N mineralization or in O₂ consumption kinetics. We found an exponential relationship between RQ values and soil pH, suggesting an excess production of CO₂ in alkaline soils. This CO₂ excess was not related to changes in substrate utilization by the microbial biomass but rather to carbonates equilibrium. The δ¹³C signatures confirmed that the CO₂ produced in soils with pH>7 originated from both organic and mineral sources. The contribution of soil carbonates to CO₂ production led to an overestimation of organic C mineralization (up to 35%), the extent of which depended on the nature of soil carbonates but not on the amount. The actual C mineralization (derived from organic C) was similar in limed and unlimed soil. The amount of C mineralized in the residue-amended soils was ten times greater than in the basal soil, thus masking the soil carbonate contribution. Residue decomposition resulted in a significant increase in soil pH in all soils. This increase is attributed to the alkalinity and/or decarboxylation of organic anions in the plant residue and/or to the immobilization of nitrate by the microbial biomass and the corresponding release of hydroxyl ions. A theoretical composition (C, O, H, N) of residue and soil organic matter is proposed to explain the RQ measured. It emphasizes the need to take microbial biomass metabolism, O₂ consumption due to nitrification and carbon assimilation yield into account when interpreting RQ data.     

An Evaluation of the Loss-on-Ignition Method for Determining the Soil Organic Matter Content of Calcareous Soils

The Loss-on-Ignition (LOI) method is widely employed for measuring the organic matter (OM) content of soil samples. There is a risk of carbonate losses when calcareous soil samples are analyzed through LOI, but this has never been investigated in detail. Moreover, a worldwide standard protocol for determining the carbonate content of soils is not available. The aims of this study were (i) to evaluate two commonly employed carbonate analysis procedures using calcareous and non-calcareous soil samples: the gravimetric method with (GMF) and without (GM) the addition of the antioxidant iron(II) chloride (FeCl₂) and the acetic acid dissolution procedure (AAD); (ii) to evaluate the effect of ignition temperature on losses of pure calcite, calcite-quartz and calcareous soil samples. We found that the average apparent carbonate content of the non-calcareous soils was greatest for the GMF method followed by the AAD procedure. The GM method showed the smallest apparent carbonate contents. For the calcite-quartz sand mixture, ignition losses started at 600°C and increased with temperature in a sigmoidal way. LOI values stabilized at 750°C when 80% of the carbon dioxide was released. We recommend the GM procedure for carbonate analysis because the apparent carbonate contents of the non-calcareous soil samples were smallest. Furthermore, we recommend an LOI temperature of 550°C because at this ignition temperature 99.8% of the total calcite fraction remains in the soil samples.     

Determination of total organic‐C in soils by an improved chromic acid digestion and spectrophotometric procedure

Abstract

An improvement to the Walkley‐Black wet digestion method for the rapid determination of organic carbon over the range 0.2–5.5% in air‐dry soil is described. It permits total recovery of the organic‐C in finely ground soil samples digested with the heat of dilution from mixing N K₂ Cr₂ O₇ with concentrated H₂SO₄. in test tubes followed by external heating from a hot‐plate digestor. The organic‐C concentrations are determined directly, as the Cr product in diluted soil digests, by absorptiometry at 600 nm with calibration against similarly treated sucrose standards in solution. For the soils tested, there were negligible interferences from carbonates, wood charcoal, coke, Fe⁺² and readily reducible Mn; Cl does not interfere with the organic‐C assay in non‐saline soils but for saline soils a correction based on 1/12 Cl^‐ assay of the soil is necessary. The present method is compared with Tabatabai and Bremner's dry combustion procedure and Allison's manometric adaptation for calcareous soils. The procedure described here does not require carbonate to be determined and is therefore simpler. In addition it is cheaper, faster and more effective in controlling interferences than dry combustion procedures.     

外加碳酸盐增加石灰性土壤密闭培养过程中CO2的释放量

The closed-jar incubation method is widely used to estimate the mineralization of soil organic C. There are two C pools (i.e., organic and inorganic C) in calcareous soil. To evaluate the effect of additional carbonates on CO2 emission from calcareous soil during closed-jar incubation, three incubation experiments were conducted by adding different types (CaCO3 and MgCO3 ) and amounts of carbonate to the soil. The addition of carbonates significantly increased CO2 emission from the soil; the increase ranged from 12.0% in the CaCO3 amended soil to 460% in the MgCO3 amended soil during a 100-d incubation. Cumulative CO2 production at the end of the incubation was three times greater in the MgCO3 amended soil compared to the CaCO3 amended one. The CO2 emission increased with the amount of CaCO3 added to the soil. In contrast, CO2 emission decreased as the amount of MgCO3 added to the soil increased. Our results confirmed that the closed-jar incubation method could lead to an overestimate of organic C mineralization in calcareous soils. Because of its effect on soil pH and the dissolution of carbonates, HgCl2 should not be used to sterilize calcareous soil if the experiment includes the measurement of soil CO2 production.     

An appraisal of soil organic C content in Mediterranean agricultural soils

Low soil organic carbon (SOC) levels in dry areas can affect soil functions and may thus indicate soil degradation. This study assesses the significance of SOC content in Mediterranean arable soils based on the analysis of a broad data set of 2613 soils sampled from Mediterranean grasslands and agricultural land. The distribution in values of SOC, pH, clay and carbonates was analysed according to different climatic areas (semi‐arid, Mediterranean temperate, Mediterranean continental and Atlantic) and with respect to six different land uses (grassland, cereal crops, olives and nuts, vineyards, fruit trees and vegetable gardens). The general trend was for low SOC in arable land and decreased with aridity. In wet areas (Atlantic and Mediterranean continental), acidic soils had a higher SOC content than did calcareous soils, whereas in the Mediterranean temperate area SOC had little relationship to soil pH. In low SOC arable soils, the SOC content was related to clay content. In calcareous arable soils of the Mediterranean temperate zone, SOC content was more closely related to carbonates than to clay. In contrast to the Atlantic area, Mediterranean grassland soils had much lower amounts of SOC than forest soils. Mediterranean calcareous and temperate acidic soils under grassland had SOC‐to‐clay ratios similar to or only slightly greater than that under a crop regime. In contrast, Mediterranean continental acidic soils under grassland had a much higher SOC‐to‐clay ratio than arable soils. This suggests a low resilience of the Mediterranean temperate and calcareous arable soils in terms of SOC recovery after the secession of ploughing, which may be a result of intensive use of these soils over many centuries. Consequently, we hypothesize that the Mediterranean calcareous soils have undergone significant changes that are not readily reversed after ploughing ceases. Such changes may be related to alterations in soil aggregation and porosity which, in turn, are associated with soil carbonate dynamics. Decarbonation processes (the depletion of active carbonates) may therefore be relevant to the reclamation of highly calcareous arable soils through fostering soil re‐aggregation. The article concludes by discussing the suitability of zero tillage, manuring or the introduction of woody species to increase SOC in calcareous arable soils that are highly depleted of organic matter.     

Quantification and depth distribution analysis of carbon to nitrogen ratio in forest soils using reflectance spectroscopy

Forest soils have large contents of carbon (C) and total nitrogen (TN), which have significant spatial variability laterally across landscapes and vertically with depth due to decomposition, erosion and leaching. Therefore, the ratio of C to TN contents (C:N), a crucial indicator of soil quality and health, is also different depending on soil horizon. These attributes can cost-effectively and rapidly be estimated using visible–near infrared–shortwave infrared (VNIR–SWIR) spectroscopy. Nevertheless, the effect of different soil layers, particularly over large scales of highly heterogeneous forest soils, on the performance of the technique has rarely been attempted. This study evaluated the potential of VNIR–SWIR spectroscopy in quantification and variability analysis of C:N in soils from different organic and mineral layers of forested sites of the Czech Republic. At each site, we collected samples from the litter (L), fragmented (F) and humus (H) organic layers, and from the A₁ (depth of 2–10 cm) and A₂ (depth of 10–40 cm) mineral layers providing a total of 2505 samples. Support vector machine regression (SVMR) was used to train the prediction models of the selected attributes at each individual soil layer and the merged layer (profile). We further produced the spatial distribution maps of C:N as the target attribute at each soil layer. Results showed that the prediction accuracy based on the profile spectral data was adequate for all attributes. Moreover, F was the most accurately predicted layer, regardless of the soil attribute. C:N models and maps in the organic layers performed well although in mineral layers, models were poor and maps were reliable only in areas with low and moderate C:N. On the other hand, the study indicated that reflectance spectra could efficiently predict and map organic layers of the forested sites. Although, in mineral layers, high values of C:N (≥ 50) were not detectable in the map created based on the reflectance spectra. In general, the study suggests that VNIR–SWIR spectroscopy has the feasibility of modelling and mapping C:N in soil organic horizons based on national spectral data in the forests of the Czech Republic.     

Improved method for removing siderite by in situ acidification before elemental and isotope analysis of soil organic carbon

Siderite (FeCO₃) is an iron carbonate mineral commonly found in sediments and soils. Similarly to other carbonates, such as calcite or dolomite, it may substantially affect the quantification of organic carbon (C) as well as determination of C isotope ratio of soil organic matter. Both analyses require effective removal of siderite by pretreatment with acid. However, little is known about the siderite removal efficiency of the acid pretreatment methods which have been previously proposed in the literature. In our study, we tested three previously proposed carbonate removal methods for siderite removal in siderite‐containing soils. Furthermore, we tested whether siderite C content in a soil sample can be detected as CO₂ evolved after H₃PO₄ addition which would allow organic C determination from the difference between total and inorganic C. None of the three tested pretreatment methods led to sufficient removal of siderite C when applied on siderite alone. Therefore, we developed a new protocol for a 4‐day treatment with 10% HCl at 25°C. At siderite content of up to 10 wt.%, the removal efficiency of our method (99–100%) was sufficient both for organic C as well as for C isotope analyses. This was further confirmed with tests on siderite‐containing soils. These showed that the method of Larson et al. ( 2008 ) developed for sediments is also suitable. However, the new protocol provides advantage in terms of less microplate manipulation, capsule overflow and oven use. We found that CO₂ is not evolved 2 minutes after H₃PO₄ addition from siderite in contrast to calcite and dolomite. This fact can be used for separate quantification of inorganic C from calcite/dolomite and siderite, e.g., in studies of their different role in soil development. We showed that siderite‐containing soils require special pretreatment procedure before organic C and ¹³C/¹²C analyses. We recommend using our protocol if techniques such as XRD or SEM‐EDS indicate the presence of siderite in soil.     

Contribution of organic amendments to soil organic matter detected by thermogravimetry

Sustainable soil management requires reliable and accurate monitoring of changes in soil organic matter (SOM). However, despite the development of improved analytical techniques during the last decades, there are still limits in the detection of small changes in soil organic carbon content and SOM composition. This study focused on the detection of such changes under laboratory conditions by adding different organic amendments to soils. The model experiments consisted of artificially mixing soil samples from non‐fertilized plots of three German long‐term agricultural experiments in Bad Lauchstädt (silty loam), Grossbeeren (silty sand), and Müncheberg (loamy sand) with straw, farmyard manure, sheep faeces, and charcoal in quantities from 3 to 180 t ha^?1 each. In these mixtures we determined the organic carbon contents by elemental analysis and by thermal mass losses (TML) determined by thermogravimetry. The results confirmed the higher reliability of elemental analysis compared to TML for organic carbon content determination. The sensitivity of both methods was not sufficient to detect the changes in organic carbon content caused by small quantities of organic amendments (3 t ha^?1 or 0.1–0.4 g C kg^?1 soil). In the case of elemental analysis, the detectability of changes in carbon content increased with quantities of added amendments, but the method could not distinguish different types of organic amendments. On the contrary, the based on analysis of degradation temperatures, the TML allowed this discrimination together with their quantitative analysis. For example, added charcoal was not visible in TML from 320 to 330°C, which is used for carbon content determination. However, increasing quantities of charcoal were reflected in a higher TML around 520°C. Furthermore, differences between measured (with TML_110–550) and predicted mass loss on ignition using both organic carbon (with TML₃₃₀) and clay contents (with TML₁₄₀) were confirmed as a suitable indicator for detection of organic amendments in different types of soils. We conclude that thermogravimetry enables the sensitive detection of organic fertilizers and organic amendments in soils under arable land use.     

五台山土壤水稳性团聚体有机碳分布特征

为揭示五台山垂直带土壤不同形态团聚体有机碳的分布特征,以五台山垂直带土壤为研究对象,于2016年8月从高海拔至低海拔对亚高山草甸土、山地草甸土、棕壤、淋溶褐土、石灰性褐土样品进行采集,并且通过湿筛法和物理分组技术获得不同土壤类型中2,2~0.25,0.25~0.053,0.053mm水稳性团聚体,进一步分析了土壤及各级水稳性团聚体的总有机碳、颗粒有机碳(POC)和矿物结合有机碳(MOC)。结果表明:亚高山草甸土、山地草甸土和棕壤均以2mm团聚体为最多,达到总水稳性团聚体的45.13%。然而,淋溶褐土和石灰性褐土中分别以2~0.25mm和0.25~0.053mm团聚体为最多,分别达到33.79%和39.95%。随着海拔高度的降低土壤有机碳含量依次降低,且不同土壤类型中,2mm和2~0.25mm团聚体有机碳含量与其对应的土壤有机碳含量呈极显著正相关关系,相关系数分别为r2mm=0.986和r2~0.25mm=0.966(P0.01)。随着土壤团聚体粒径的减小,亚高山草甸土、山地草甸土、棕壤的POC含量呈现下降趋势,而淋溶褐土和石灰性褐土的POC含量呈现升高趋势。亚高山草甸土、山地草甸土、棕壤的MOC含量都以2mm团聚体为最大,淋溶褐土和石灰性褐土分别以2~0.25mm和0.25~0.053mm团聚体的MOC含量为最大。各土壤及团聚体中MOC的含量要明显大于POC的含量,而且在土壤和各级大团聚体中二者呈现正相关关系(P0.05)。此外,各土壤POC和MOC的含量与土壤有机碳含量也呈现正相关关系(P0.05)。因此,随着海拔高度的降低,各土壤团聚体组成由大团聚体向微团聚体转变,亚高山草甸土、山地草甸土、棕壤的碳截获能力强于淋溶褐土和石灰性褐土。     

Organic carbon in soils of Germany: Status quo and the need for new data to evaluate potentials and trends of soil carbon sequestration

Uncertainties in estimates of soil carbon (C) stocks and sequestration result from major gaps in knowledge of C storage in soils, land‐use history, the variability of field measurements, and different analytical approaches applied. In addition, there is a lack of long‐term datasets from relevant land‐use systems. As in many European countries, a national database on soil organic carbon (SOC) including all relevant information for the determination of soil C stocks is likewise missing in Germany. In this paper, we summarize and evaluate the present state of knowledge on organic‐C contents/pools in soils of Germany and discuss the need for the acquisition and access to new data on soil organic carbon. Despite the number of agricultural sites under permanent soil monitoring, regional surveys on SOC, comprehensive ecosystem studies, and long‐term field experiments, there is a striking lack of data in Germany particularly with regard to agricultural soils. Apart from a missing standardization of methods and homogeneous baseline values, the implementation of a periodic, nation‐wide soil inventory on agricultural soils is required in order to simultaneously record information on land use, land‐use change, and agricultural practice. In contrast, the existing national inventory of forest soils provides information on C‐stock changes in forest soils, although there is some concern with regard to the representativeness of the sampling design to adequately address the problem of spatial heterogeneity and temporal variability. It is concluded that the lack of comprehensiveness, completeness, actuality, data harmonization, and standardized sampling procedures will further prevent the establishment of a SOC database in Germany with regard to the monitoring of trends in soil C pools and fluxes and the assessment of long‐term C‐sequestration potentials of soils under different land use. A future soil inventory should represent the heterogeneity of organic matter through functionally different SOC pools, topsoil characteristics as well as content, pool, and flux data for the deeper mineral‐soil compartments.     

Agrophysical assessment of alluvial calcareous soils of the Çumra region of Central Anatolia in Turkey

Some physical (density, coefficient of filtration, particle-size composition, etc.) and chemical (contents of carbonates, organic carbon, nitrogen, etc.) properties of an alluvial calcareous soil were studied in Central Anatolia (Konya province, Çumra region). These heavy-textured (medium clay) soils with a low content of organic carbon (less than 1%) have favorable agrophysical properties due to the stable structure of the pore space. The studies of the water regime of soils under drop irrigation confirm the favorable hydrological properties of these soils. The use of the known agrophysical estimates (after Medvedev, the index of the optimal water regime, etc.) has revealed the high dispersal of the data related to the low humus content in these heavy-textured soils. The favorable structure of the pore space is suggested to be stipulated by the active activity of the numerous and diverse representatives of soil biota. Four phyla predominate in the microbio-logical composition of the soils studied; among them, Actinobacteria is the dominant. The composition of this phylum is dominated by the elevated number of both higher (Streptomyces) and lower (three species of Rhodococcus) actinobacteria. The high biodiversity of bacteria against the background of their great total number and the developed trophic interactions in the microbial community promote the well-balanced production of specific metabolites, including gaseous ones (CO₂, H₂). This circumstance allows this clayey soil to function rather actively while protecting the pore space against compaction and maintaining the optimal density, porosity, and hydrological properties.     

Loss‐on‐ignition as an estimator of soil organic carbon in a‐horizon forestry soils

Abstract

The determination of soil organic matter by wet digestion techniques is a slow and laborious analysis. Loss‐on‐ignition (LOI) provides a simple alternative technique for the estimation of soil organic carbon in non‐calcareous A horizon soils of the Natal midlands and Zululand forestry regions. Using multiple regressional techniques, the relationships between loss‐on‐ignition, Walkley organic carbon and soil texture for 55 soils were determined over a range of ignition temperatures. The relationships hold best for soil samples with relatively low organic carbon contents (< 5%). The optimum temperature for ignition was found to occur at 450°C and resulted in the relationship: Soil organic carbon = 0.284*LOI percent. No advantage is gained through ignition at higher temperatures due to the loss of clay mineral structural water, even if the soil texture is accurately known.     

Availability and speciation of cadmium added to a calcareous soil under various managements

Potential risks for human health and adverse effects on soil quality caused by accumulation of cadmium (Cd) in soil at concentrations around or exceeding current European Union (EU) permitted limits have long been recognized. We have assessed availability and partitioning of Cd in a Mediterranean calcareous soil under four management regimes. Cadmium was added as a single pulse of CdSO₄ at the maximum Cd concentration established by the EU for sludge‐amended agricultural soils and concentrations exceeding the mandatory limits. Soils were treated with 0, 3, 10 and 50 mg Cd kg^?1 soil, incubated moist and analysed at selected times up to 600 days. Cadmium availability and distribution in soil were studied by neutral electrolyte and sequential extractions. During the incubation, the availability of Cd was not strictly dependent on the amount of metal added as the exchangeable fractions were similar shortly after the additions of Cd regardless of its initial concentration. Sequential extractions showed that for concentrations of 3 and 10 mg Cd kg^?1 soil Cd was evenly distributed among the soil phases, and its mobility was reduced mainly by adsorption on carbonates. At Cd concentrations exceeding 10 mg Cd kg^?1 soil a residual fraction appeared, perhaps from precipitation of Cd. Most of the Cd was associated with carbonates; land management and organic matter content had no major effects on the Cd distribution among different soil phases. The extraction protocols were effective for studying the fate of Cd in this calcareous soil as almost all of the Cd added was recovered. However, the introduction of a preliminary step with buffered NH₄NO₃ improved the determination of the most labile pools. Availability of Cd in calcareous soils estimated with reference methods appeared to be very small even when its total concentration far exceeded the current EU limits.     

用激光衍射法评价有机物和和碳酸盐对土壤团聚的作用

>Aggregation in many soils in semi-arid land is affected by their high carbonate contents.The presence of lithogenic and/or primary carbonates can also inffuence the role of soil organic matter(SOM) in aggregation.The role of carbonates and SOM in aggregation was evaluated by comparing the grain-size distribution in two carbonate-rich soils(15% and 30% carbonates) under conventional tillage after different disaggregating treatments.We also compared the effect of no-tillage and conventional tillage on the role of these two aggregating agents in the soil with 30% of carbonates.Soil samples were treated as four different ways:shaking with water(control),adding hydrochloric acid(HCl) to remove carbonates,adding hydrogen peroxide(H2O2) to remove organic matter,and consecutive removal of carbonates and organic matter(HCl + H2O2),and then analyzed by laser diffraction grain-sizing.The results showed that different contributions of carbonates and SOM to aggregate formation and stability depended not only on their natural proportion,but also on the soil type,as expressed by the major role of carbonates in aggregation in the 15% carbonate-rich soil,with a greater SOC-to-SIC(soil organic C to soil inorganic C) ratio than the 30% carbonate-rich soil.The increased organic matter stocks under no-tillage could moderate the role of carbonates in aggregation in a given soil,which meant that no-tillage could affect the organic and the inorganic C cycles in the soil.In conclusion,the relative role of carbonates and SOM in aggregation could alter the aggregates hierarchy in carbonate-rich soils.     

Comparison of Three Methods for Measurement of Soil Organic Carbon

Quantification of soil organic carbon (SOC) is an important element in the assessment of the carbon sequestration potential of soils in tree-based intercropping (TBI) systems. The organic carbon (OC) concentrations of soils in TBI systems often differ from those in conventional agricultural systems due to the additional C inputs from litter fall and roots. However, the presence of soil inorganic carbon (SIC) can confound the measurements of SOC. This study compared three methods of measuring SOC: (i) measurement of the total soil C (TC) in one subsample and, after treatment in a muffle furnace (575 °C) for 24 h, measurement of SIC in another subsample; (ii) SOC measured after fumigation with 12 M hydrochloric acid (HCl) to remove SIC; and (iii) SOC measured after digestion with 0.73 M H₂SO₃ to remove SIC. The TC, SOC, and SIC concentrations were determined by combustion. A correction factor was applied to express SIC and SOC concentrations on an original, untreated soil basis. Measurement of SOC by the muffle furnace method resulted in the greatest SOC concentrations for Populus spp. (hybrid poplar) for samples from two of the three depths (0–10 and 20–40 cm). Measurement of SOC by the HCl fumigation and H₂SO₃ digestion methods were highly correlated, suggesting complete removal of SIC with minimal oxidation of SOC. These results have implications for the method of measuring SOC in calcareous soils under coniferous and deciduous tree species to a depth of 40 cm.     

Utilization of Compost Increases Organic Carbon And Its Humin,Humic and Fulvic Acid Fractions In Calcareous Soil

Organic carbon sustainability in a gravelly calcareous soil is a great challenge under the humid conditions of south Florida. The beneficial effects of compost utilization on soil fertility prompted an investigation on (i) accumulation of total organic carbon and (ii) the soil organic carbon (SOC) in humin, humic acid (HA) and fulvic acid (FA) fractions in a gravelly calcareous soil amended with composts or inorganic fertilizer. In 1996 and 1998, compost from municipal solid waste (MSW) (100% MSW), Bedminster cocompost (75% MSW and 25% biosolids) and biosolids compost (100% biosolids) at 72, 82.7 and 15.5 Mg ha^?1, respectively, were each incorporated in soil beds and inorganic fertilizer (6-2.6-10) NPK at 2.8 Mg ha^?1. A control (no amendment) treatment was also included. Total organic carbon and various fractions of soil organic carbon were determined in two depths (0-10 and 10-22 cm) for both soil particles (< 2mm) and pebbles (> 2mm). Inorganic and organic soil amendments had decreased soil pH and increased soil electrical conductivity (EC) 19 months from initial application. Total organic carbon contents in soil particle were 4-, 3-, and 2-fold higher in MSW compost, Bedminster cocompost and biosolids compost treatments, respectively, than those in fertilizer treated or non-treated soils. MSW compost increased total organic carbon in pebbles by 4- and 3-fold in the 0-10 and 10-22 cm deep layers, respectively, more than other treatments. The soil organic carbon accumulation decreased with depth in all treatments in soil particles, but did not in pebbles. Amending soils with MSW compost significantly increased the organic carbon in humin, HA and FA fractions more than those treated with inorganic fertilizer or non-amended. MSW compost has a potential to be used as a soil amendment to increase and sustain the organic carbon in calcareous soils of south Florida.     

Classification of anthrosols with vitric/andic properties derived from lignite ash

To test the applicability of the Soil Reference Base of Soil Resources (ISSS/ISRIC/FAO, 1998. World Reference Base for Soil Resources, World Soil Resources Report 84, FAO, Rome) for soils derived from anthropogenic substrates, soils developed on lignite ashes in Germany which have some similarities with andosols were compared with natural volcanic soils from different countries. Soil parameters used for comparison were bulk density, clay content, Al_o+0.5 Fe_o, and P-retention, as they serve as diagnostic criteria to define either vitric or andic horizons. For Al_o+0.5 Fe_o, and P-retention, there was no statistically significant difference between both soil groups, the bulk densities of the lignite ash-derived soils were even significantly lower than those of the natural volcanic soils. Moreover, pH, total organic carbon, cation exchange capacity as well as the contents of carbonates and gypsum were collated and differences emerged between both soil groups concerning the contents of carbonates, gypsum and total organic carbon. In case of the lignite ash-derived soils, these parameters as well as the contents of oxalate soluble oxides were strongly influenced by the composition of the anthropogenic parent material. Up to now, such soil materials are not included as soil-forming materials in the World Reference Base for Soil Resources. We therefore suggested the introduction of a new diagnostic soil material, the so-called technogenic soil material into the anthropogeomorphic soil materials and to introduce “technogenic anthrosols” as a new reference subunit. In our proposition, technogenic materials are defined as anthropogeomorphic materials which are formed by technical processes including a distinct degree of transformation and/or new formation of soil-forming materials. Soil materials are categorised as “technogenic” when they consist of more than 70% (by volume) of soil material derived from technical processes like, e.g. combustion products of fossil energy sources, sewage sludges, blast furnace slags, etc.To include as much information as possible into the name of a soil, we developed a concept of reference soil series for the WRB combining pedogenetic and lithogenic information. Within this concept, these soils should be considered to be a subunit of anthrosols (vitri- or andi-technogenic anthrosols) and the specific properties of the soil-forming material (coaly, calcaric, gypsiric) should be given as additional information as Reference Soil Series as well as texture and kind of parent material.