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1.
The island of Milos (Greece), part of the South Aegean volcanic arc with a typical Mediterranean climate, is covered with volcanic deposits of different ages. The objective of this study was to investigate the physicochemical and mineralogical properties of the soils developing on these volcanic deposits and their classification. Samples were taken from seven locations of soil on different parent material and of different ages. There were substantial differences in their particle size distribution, with sand ranging from 19% to 92%, silt from 3.5% to 50%, and clay from 5% to 46%. Organic matter content was low (< 2.0%). The soil pH ranged from 5.6 to 8.0. In two of the profiles, CaCO3 equivalents of 1.4% to 24.6% were found and a calcic horizon identified. The cation exchange capacity (CEC) and specific surface area (SSA) varied between profiles ranging from 3 cmol(+) kg− 1 to 47 cmol(+) kg− 1 and 30 m2 g− 1 to 380 m2 g− 1, respectively. The soils exhibited high base saturation. The amounts of Al, Fe and Si extracted with ammonium oxalate (Αlo, Feo and Sio) were particularly low (< 0.1%, < 0.17%, and < 0.1%, respectively) which demonstrates the absence of amorphous clay-silicate minerals (allophane). Fe extracted with dithionite citrate bicarbonate — DCB (Fed) was greater than Feo sharing the dominance of crystalline Fe oxides. Al and Si extracted with hot 0.5 M NaOH (Al2Ο3NaOH and SiΟ2NaOH) and with Τiron-C6H4Na2O8S2, (Al2Ο3Τ and SiΟ2Τ). SiΟ2NaOH and SiΟ2Τ were particularly high (mean values 3.4% and 4.5%, respectively), showing that amorphous silica was present. The clay fraction of the soil was dominated by the presence of 2:1 (vermiculite and smectite) and 1:1 (kaolinite) clay-silicates. Alo+ 1/2Feo was low (< 0.18%), while the P-retention in most soils was less than 15%. These soils do not exhibit andic properties and hence cannot be classified as Andisols. The silica saturation index (ISS) may be used for these soils to describe a pedogenetic environment rich in Si which favours the formation of pedogenic amorphous silica. The climate is the major determinant of the evolution of these soils.  相似文献   

2.
Recent studies with Andisols show that the carbon (C) stabilization capacity evolves with soil age relative to the evolution of the mineral phase. However, it is not clear how soil mineralogical changes during pedogenesis are related to the composition of soil organic matter (SOM) and 14C activity as an indicator for the mean residence time of soil organic matter (SOM). In the present study, we analyzed the contribution of allophane and metal–SOM complexes to soil C stabilization. Soil organic matter was analyzed with solid-state 13C nuclear magnetic resonance spectroscopy. Additionally, the soil was extracted with Na-pyrophosphate (Alp, Fep) and oxalate (Alo, Sio, and Feo). Results supported the hypothesis that allophane plays a key role for SOM stabilization in deep and oldest soil, while SOM stabilization by metal (Al and Fe) complexation is more important in the surface horizons and in younger soils. The metal/Cp ratio (Cp extracted in Na-pyrophosphate), soil pH, and radiocarbon age seemed to be important indicators for formation of SOM–metal complexes or allophane in top- and subsoils of Andisols. Changes in main mineral stabilization agents with soil age do not influence SOM composition. We suggest that the combination of several chemical parameters (Alp, Fep and Cp, metal/Cp ratio, and pH) which change through soil age controls SOM stabilization.  相似文献   

3.
Abstract

Phosphate (P) sorption characteristics of six natural Ghanaian Oxisols, selected because of their hydrological and topographical suitability for agriculture, were evaluated. Availability of P appears to be adequate for half of the soils as suggested by the Bray P1 test and determination of the standard P requirement (SPR), i.e., the amount of P sorbed at a concentration of 0.2 ppm P (6.46 μM). The SPR was found to be very closely related to Pmax (Langmuir P sorption capacity), which in turn, was significantly correlated with oxalate‐extractable aluminum (Al) (Alo) and iron (Fe) (Feo) and related (not significantly) to the difference between dithionite‐citrate‐bicarbonate‐extractable Fe (Fed) and oxalate‐extractable Fe. Accordingly, Pmax is fairly well predicted by the model of Borggaard: Pca]e=0.211#lbÀlo+0.115#lbFeo+ 0.05#lb(Fed‐Feo)+0.3, except for one soil strongly enriched in Fe oxides, mainly goethite. This goethite was found by X‐ray diffraction analysis to consist of crystals larger than normally found for pedogenic Fe oxides. The difference between Pmax and Pcalc for this soil could, therefore, be attributed to the occurrence of these large Fe oxide crystals, because P sorption will decrease with increasing crystal size (decreasing specific surface area).  相似文献   

4.
Minerals with large specific surface areas promote the stabilization of soil organic matter (SOM). We analysed three acidic soils (dystric, skeletic Leptic Cambisol; dystric, laxic Leptic Cambisol; skeletic Leptic Entic Podzol) under Norway spruce (Picea abies) forest with different mineral compositions to determine the effects of soil type on carbon (C) stabilization in soil. The relationship between the amount and chemical composition of soil organic matter (SOM), clay content, oxalate‐extractable Fe and Al (Feo; Alo), and dithionite‐extractable Fe (Fed) before and after treatment with 10% hydrofluoric acid (HF) in topsoil and subsoil horizons was analysed. Radiocarbon age, 13C CPMAS NMR spectra, lignin phenol content and neutral sugar content in the soils before and after HF‐treatment were determined and compared for bulk soil samples and particle size separates. Changes in the chemical composition of SOM after HF‐treatment were small for the A‐horizons. In contrast, for B‐horizons, HF‐soluble (mineral‐associated) and HF‐resistant (non‐mineral‐associated) SOM showed systematic differences in functional C groups. The non‐mineral associated SOM in the B‐horizons was significantly depleted in microbially‐derived sugars, and the contribution of O/N‐alkyl C to total organic C was less after HF‐treatment. The radiocarbon age of the mineral‐associated SOM was younger than that of the HF‐resistant SOM in subsoil horizons with small amounts of oxalate‐extractable Al and Fe. However, in horizons with large amounts of oxalate‐extractable Al and Fe the HF‐soluble SOM was considerably older than the HF‐resistant SOM. In acid subsoils a specific fraction of the organic C pool (O/N‐alkyl C; microbially‐derived sugars) is preferentially stabilized by association with Fe and Al minerals. Stabilization of SOM with the mineral matrix in soils with large amounts of oxalate‐extractable Alo and Feo results in a particularly stable and relatively old C pool, which is potentially stable for thousands of years.  相似文献   

5.
Andosol formation involves the rapid, abundant and in situ formation of non‐crystalline materials from tephra deposits. A large amount of humus complexed with Al also accumulates in the A horizons. As these materials are rich in Al or Fe compared to the parent tephra, the concentrations of the major and minor elements change significantly during Andosol formation. The objectives of this study were to examine how the rock type of the tephra and its weight loss during the formation process affect the changes in the element concentrations of Andosols. A total of 95 samples with different rock types from 18 pedons of Andosols in Japan were used to determine the total concentrations of 54 elements. Principal component analysis suggested that the degree of weathering and the rock types of parent tephra are the important factors in the variation of the element concentrations in Andosols. Three rock types, dacitic, andesitic and basaltic‐andesitic, were identified from the V and Zn contents of ferromagnetic minerals separated from the Andosol samples. Basaltic Andosols were identified from the abundant coloured volcanic glass and olivine in the sand fraction. Regarding concentrations of 41 elements, at least one group based on rock type was significantly different from one to three other groups at the P= 0.05 level. The content of oxalate‐extractable Si (Sio), Al (Alo) and Fe (Feo) was used as an index to show the extent of Andosol development. Relatively strong correlations between the element concentrations and Sio, Alo and Feo as well as other weathering indices were found in the andesitic samples. Among these elements, at least 27 (Be, Al, Ti, Fe, Y, Zr, Nb, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, Tl, Pb, Th and U) were enriched in the Andosols and the increases in these concentrations were related to total weight loss due to soil formation processes.  相似文献   

6.
We studied the mineralogical properties of Andisols of the Kitakami mountain range. Soils of the northern and central parts of the mountain range contained higher levels of acid oxalate extractable silicon (Sio), aluminum (A1o), and iron (Feo) but smaller amounts of sodium pyrophosphate-extractable aluminum (Alp), iron (Fep), and carbon (Cp) than those of the southern part. Consequently, the soils of the northern and central parts of the mountain range contained large amounts of allophane and ferrihydrite whereas in the soils of the southern part A1 (Fe)-humus complexes and 2:1 and 2:1:1 clays predominated. The amount of sand (20-2,000 μm) in the soils tended to decrease sharply from the north to the south of the mountain range. The soils of the northern and central parts of the mountain range contained larger amounts of heavy minerals in their fine sand fraction (20-200 μm). The soils of the southern part, on the other hand, contained larger amounts of fine-grained quartz (2-20 μm). All the soils of the mountain range contained substantial amounts of volcanic glass in their sand fraction. However, on a total soil basis, the amount of volcanic glass in the soils decreased from the north to the south of the mountain range and the trend was parallel to that of the sand content of the soils. From these results, we concluded that (i) the soils of the northern and central parts of the mountain range were derived mainly from tephras and (ii) the soils of the southern part were strongly influenced by long-range eolian dust.  相似文献   

7.
Organic carbon stocks and soil erodibility in Canary Islands Andosols   总被引：3，自引：0，他引：3  
Soil organic carbon (SOC) plays a key role in the structural stability of soils and in their resistance against erosion. However, and as far as andic soils are concerned, these mechanisms and processes, as well as the influence of the different types of SOC on aggregate stability, are not fully understood. The targets of this paper are: (i) to determine the content and forms of SOC in Andosols under evergreen forest vegetation [laurel (Laurus) and heather (Erica) forest] and (ii) to find out the role of soil organic matter (SOM) in the aggregate stability and in the resistance of Andosols to water erosion. Soil samples have been collected in 80 sites in a 40 km2 area under udic soil moisture regime. In them, fulvic and humic acids, Walkley–Black SOC, pyrophosphate-extractable SOC, Fe and Al, potassium sulphate extractable SOC, dissolved SOC, acid oxalate-extractable Fe, Al and Si, USLE K-factor and aggregate stability have been determined. The Andosols over volcanic ash are Aluandic Andosols (non-allophanic Andosols), whereas over basaltic lava flows are Silandic Andosols (allophanic Andosols). The surface (0–30 cm) samples analyzed contain 9.5–30 kg C m− 2 being significantly higher in allophanic Andosols (p < 0.5). Organic carbon adsorbed onto the mineral fraction (extractable pyrophosphate, Cp) accounts for 35–55% of the total SOC. All samples show a high stability to slaking and raindrop impact, being the first one highly correlated (r = 0.6) with pyrophosphate extractable C (Cp), Fe (Fep), and Al (Alp) in allophanic Andosols, unlike non-allophanic ones. The stability to raindrop impact correlates with pyrophosphate extractable C (Cp) and Fe (Fep) in both types of soils (r = 0.3–0.6, p < 0.05). These findings suggest that the high stability to both slaking and water-drop impact is due to the occurrence of allophane–Fe–OC complexes, rather than to the total OC, and the active Fe and Al forms, generated by the weathering of volcanic materials, constitute an essential constituent responsible for C sequestration and resistance to degradation in these soils.  相似文献   

8.
In previous studies, Al extracted by acid ammonium acetate (Ala) or Na-pyrophosphate (Alp), rather than silt or clay content and climate conditions, was the most important factor that controls organic matter (OM) levels in volcanic soils. Here, the hypothesis was tested that Ala is a comparable method (as much as CuCl2) to quantify the proportion of Al bound to OM in allophanic soils. As far as we know, there are no previous antecedents in which selective dissolution method has been compared with this extractant. Secondly, we examine the effects of (a) Al, (b) silt plus clay content (particles size 0-53 µm) and (c) clay mineralogy on the control of organic carbon (OC) level in Chilean volcanic soils. This was achieved by sampling 16 soils series (11 Andisols, one Alfisol and four Ultisols, USDA classification) including 48 soil pedons up to 0.4 m depth. Soils were analyzed for Ala, Alp, oxalate (Alo, Sio and Feo), cold NaOH (Aln) and un-buffered salts, CuCl2 (AlCu), LaCl3 (AlLa) and KCl (Alk). We also measured the Al-humus as soluble C fraction after pyrophosphate extraction and the C associated to the silt plus clay fraction after sonication and gravity decantation. The statistical package (S)MATR was used to examine bivariate linear regressions among soil properties by computing the standardized major axis (SMA). Our results indicate that Ala had a good correspondence with Alp (R2 = 0.76) in the top soil with Ala/Alp ratio of 0.19 and both extractans presented significant and positively relationship with soil OC (R2 > 0.62). Acid ammonium acetate was as effective as AlCu to determine the Al-OM in allophanic soils. It is cheaper than AlCu and Alp and 0.5 h shaking is required compared to 2 h of AlCu and 16 h of Alp. The efficiency of the extraction was: Aln ≥ Alo > Alp > AlCu ≥ Ala > AlLa > Alk. We also found that allophane content (estimated by Al/Si ratio) was strongly correlated (R2 = 0.82) with the OC in the fine silt plus clay and that Al-humus together with C in the finest particles explained (R2 > 0.60) the largest proportion of variation of soil OC across studied soils.  相似文献   

9.
Andr Eger  Allan Hewitt 《CATENA》2008,75(3):297-307
This study focuses on soils in a mountainous catchment area located in the eastern part of the Southern Alps, South Island, New Zealand. The objective was to check the soils for non- or poorly crystalline constituents (metal organic complexes, short-range-order minerals) and if there is a relationship between pedogenesis and aspect and more recent landscape history. The morphology of the soils indicates brown soils (dystric cambisols, dystrudepts) with only few signs of podsolisation. In contrast, selected chemical properties of the soils reveal very strong weathering and leaching. Feo/Fed ratios are high and exceeding 0.6 in almost every soil horizon. Oxalate-extractable aluminium and silicon show prominent peaks in the lower subsoil horizons with 1.76–2.52% Alo and up to 0.68% for Sio on southern aspects. This is considerably higher than the values measured for soils on northern aspects (0.59% to 1.07% Alo, max. 0.26% Sio). This aspect relationship is also applying to phosphate retention reaching values of more than 90% on southern aspects and not more than 70% for northern aspects. Additionally, significant movement of organic matter in soils on southern aspects is evident by measurements of organic carbon and pyrophosphate-extractable Al and Fe. Thus soil formation can be regarded as more advanced on southern aspects. Allophane in association with organic matter can be considered as an important constituent in southern aspect subsoils being responsible for the typical andic properties. Metal-humus complexes and ferrihydrite are of subordinate significance. Considering the actual soil forming conditions under scrub-grassland (esp. soil acidity), it is unlikely that weathering and leaching is still strong enough today to allow significant podsolisation and the formation of short-range-order minerals. Under consideration of existing soil data from other studies it is proposed that these components and the podsolisation features are relicts caused by more acidic conditions under former forest cover which supported a stronger weathering and leaching.  相似文献   

10.
The stabilization of SOM by Al–humus complexes and non-crystalline minerals is a key issue to explain the soil-C variability and the biogeochemical processes that determine the fate of soil C following land-use/cover change (LUCC) in volcanic landscapes. In an altitudinal gradient of volcanic soils (2550–3500 masl), we quantified the total soil C (CT) concentrations and stocks in soil pits sampled by genetic horizons. We performed analyses at landscape and local scales in order to identify and integrate the underlying environmental controls on CT and the effects of LUCC. We selected four sites, two on the upper piedmont, one on the lower mountain slope and one on the middle mountain slope at Cofre de Perote volcano (eastern central Mexico) where temperate forests are the natural vegetation. At each site we selected three to five units of use/cover as a chronosequence of the LUCC pathways. In each soil horizon chemical characteristics (i.e. N, C/N ratio, pH, exchangeable bases) were determined and mineralogical properties were estimated from selective Al, Fe and Si oxalate and pyrophosphate extractions (i.e. the Alp/Alo ratio, the active Al related to non-crystalline minerals as Alo ? Alp, the allophane concentration, and the non-crystalline Al and Fe minerals as Alo + 1/2Feo). At landscape scale, the Al–humus complexes were strongly related to the CT concentration in topsoil (A horizons) but this relationship decreased with depth. In turn, the non-crystalline minerals and the C/N ratio explained the variability of the CT concentrations in C horizons. At local scale, CT concentrations and stocks were depleted after conversion of forest to agriculture in Vitric Andosols at the upper piedmont but this was not observed in Silandic Andosols. However, in Vitric Andosols the reduction of the CT stocks is partially recovered throughout the regeneration/reforestation processes. The results suggest that the lower vulnerability of Silandic Andosols than Vitric Andosols to changes in the CT after LUCC is due to the higher levels of SOM stabilized by Al–humus complexes and non-crystalline minerals in the Silandic soils. Furthermore, the importance of the allophane to explain the CT stocks in the Silandic Andosols of the middle slopes suggests that the CT stabilized by this mineral fraction in the subsoil adds an important fraction of the CT to the estimates of the stocks.  相似文献   

11.
Abstract

Highly calcareous soils are abundant in Iran. The calcium carbonate equivalent (CCE) of these soils reach up to 650 g kg?1. Although phosphorus (P) fertilizer is being widely used in these soils, little information, if any, is available about P status in such soils. The objectives of this study were to 1) determine inorganic P forms in 18 surface soils of southern Iran, 2) study P readsorption during different stages of fractionation schemes, 3) assess the ability of NaOH to extract aluminum (Al)‐P, and 4) evaluate the relationships between P availability indices and inorganic P forms. Eighteen soil samples with a wide range of physicochemical properties were selected for this study. Inorganic P forms was determined by sequential extraction with NaHCO3, NH4OAc, NH4F, NaOH, citrate dithionite (CD), and H2SO4, which are referred to as Ca2‐P, Ca8‐P, Al‐P, Fe‐P, occluded P (O‐P), and Ca10‐P. Phosphorus readsorption in different stages was determined by 1 M MgCl2. Furthermore, a fractionation scheme without an NH4F step was used to evaluate the ability of NaOH to extract Al‐P. NaHCO3 (Olsen‐P) and MgCl2‐extractable P (Exch‐P) were regarded as P-availability indices. The abundance of different P forms was in the order Ca2‐P<Fe‐P<Al‐P<O‐P<Ca8‐P<Ca10‐P. Ca2‐P was highly correlated with Olsen‐P and Exch‐P. Ca2‐P, Olsen‐P, and Exch‐P showed a relationship with CCE, citrate–bicarbonate–dithionite extractable Fe (Fed), and Al (Ald). Phosphorus readsorption appeared to be important only in the Ca8‐P step, and the content of readsorbed P was related to Ca8‐P, CCE, and clay content of the soils. In the present study, Al‐P and Fe‐P accounted for 10 and 5% of the sum of the inorganic P fractions, respectively, and Fe‐P showed a strong relationship with Feo, whereas Al‐P showed a significant relationship with oxalate‐extractable Al (Alo) and Ald. It was found that one extraction with NaOH is not a good indicator for Fe‐ and Al‐P, and the ability of NaOH to extract Al‐P was reduced with increase in Al‐P content.  相似文献   

12.
C.A. Igwe  M. Zarei  K. Stahr 《CATENA》2009,77(3):232-237
The stability of microaggregates in soils as opposed to its dispersion is a very important soil phenomenon that checks degradation arising from unguided tillage and soil erosion. Ten soils from southeastern Nigeria were sampled from their typical A and B horizons for the study. The aim was to identify the extent of colloidal stability of the soils and the forms of Fe and Al oxides in the soils contributing to their stability. The soils are mostly Ultisols and Inceptisols formed on sandstones and shale parent materials. The soils are low in soil basic cations including the soil organic carbon (SOC). The major clay mineral is kaolinite while the soil is acid in reaction. The various forms of soil Fe and Al oxides are high with the total forms of Fe and Al being most dominant and > dithionite extracted Fe and Al > oxalate extracted Fe and Al > pyrophosphate extracted Fe and Al. The water-dispersible clay and silt (WDC) and (WDSi) which are index of dispersion in most soils are low to medium thus reflecting in the low to medium dispersion ratio (DR). The clay flocculation index (CFI) and aggregated silt + clay (ASC) were moderate to high implying the high potential stability of the soils. Soil organic carbon did not seem to be contributing much to the stability of the microaggregates while oxalate and pyrophosphate extractable Fe (Feox, Fep) and to some extent total Al (Alt) were among the different forms of oxides that act as aggregating agents. We propose here that rather than SOC acting as a disaggregating agent in the soils, it might have acted in association with these oxides in a linkage or bridge such as C–P–OM–C to ensure stability of the soils.  相似文献   

13.
There has been less concern about soil mineralogical alteration than about soil physical, chemical and biological changes induced by termite nest-building activity. Furthermore, much less attention has been paid to free sesquioxides than to phyllosilicate minerals. In the present study, we conducted field morphological observations and selective dissolution analysis to characterize free sesquioxides in termite (Macrotermes bellicosus) mounds as compared with surrounding pedons in different toposequence positions, i.e., seasonally flooded valley bottom, hydromorphic fringe and well-drained upland sites. Distinctive redoximorphic features, such as surface yellowish layers on mound structures from the fringe site, indicate possible alteration of iron sesquioxide forms in the mounds due to the transportation of soil from reductive (aquic subsoil) to oxidative (epigeal mound) environments by the nest-building activity of M. bellicosus. On the other hand, the iron-soluble content in the dithionite-citrate-bicarbonate (DCB) system (Fed) was generally higher in the mound structures than at the adjacent sub-surface (Ap2) horizon at each toposequence position, while there was less difference in the content of acid ammonium oxalate (AAO) extractable iron (Feo) as compared to Fed. As a consequence, the iron activity index (Fed/Feo ratio) was found for the most part to be lower in the mound structures than in the neighboring Ap2 horizon. In addition, the content of Fed, AAO-soluble Al (Alo) and DCB-extractable Al (Ald) was significantly correlated with clay content in these soils. These findings suggest that M. bellicosus preferentially collects clay particles, probably from the clay-rich subsoils, such as the argillic horizon, which has been formed by the co-migration of phyllosilicate minerals and relatively crystalline sesquioxides. The species then likely incorporates them into the mounds, which induces an increase in the Fed content relative to that of Feo, resulting in a decreased iron activity index in the mound structures.  相似文献   

14.
Iron, Al, and Mn were extracted by oxalate and dithionite from two Brown Mediterranean Soils, two Red Mediterranean Soils, one Vertisol and one Gley soil, all derived from basalt or scoria in the sub-humid and humid Mediterranean regions of the Golan Heights. Ratios of oxalate: dithionite extracted iron (Feo:Fed) were low in all soils, indicating that the predominant form of free iron is crystalline. Feo accumulates in the argillic B horizons of the Mediterranean soils, while Fed accumulates in the surface horizons. A large part of the free iron oxide in the surface horizons of Mediterranean soils is associated with non-clay fractions. While manganese behaves in a manner somewhat similar to that of iron, no definite trends could be discerned in the vertical distribution of free aluminium. In the Vertisol, Feo and Mno accumulate in the subsoil. Fed and Mnd increase slightly with soil depth. In the Gley soil, amorphous iron accumulates in the surface horizon, total free iron in the bottom horizon. Both amorphous and total free Mn had been depleted from the upper horizons of the Gley soil.  相似文献   

15.
Alpine wetlands and meadows across the Three Rivers Source Region (TRSR) store high soil organic carbon (SOC). However, information on factors affecting SOC storage is scanty. Herein, we investigated SOC storage and explored factors affecting SOC storage, including climate, soil properties and above- and belowground biomass, using 50 soil profiles across the TRSR on the Tibetan Plateau. The SOC storage was 491.9 ± 158.5 Tg C and 545.2 ± 160.8 Tg C in the TRSR alpine wetlands and meadow, respectively. The SOC stock was positively correlated with the mean annual precipitation. However, no significant correlation between SOC stock and mean annual temperature was observed, as opposed to the global trend. In addition, SOC stock was positively correlated with both the aboveground biomass (AGB) and belowground biomass (BGB). Soil pH indirectly affected SOC stock, while SOC stock positively correlated with Al and Fe oxyhydroxides. Compared with vegetation biomass and climatic factors, soil properties, including soil pH and Al and Fe oxyhydroxides (Alo and Feo), affected not only SOC stock variation but also affected the impact of vegetation and climatic factors on SOC stock. Climate factors, AGB, BGB, soil pH, Alo and Feo jointly accounted for 59% of SOC stock variation in alpine wetlands and 64% of SOC stock variation in alpine meadow. This study suggests that soil properties are the dominant factors affecting SOC variation in alpine wetlands and meadow on the Tibetan Plateau.  相似文献   

16.
C.W. Childs  R.L. Parfitt  R. Lee 《Geoderma》1983,29(2):139-155
Chemical and mineralogical data are presented for three Spodosols (podzols) and a related Inceptisol (yellow-brown loam). Allophane with an Al/Si atomic ratio close to two is identified in the B horizons of all four soils, and minor amounts of imogolite are present in association with allophane in all but one soil where small-particle gibbsite occurs. Parent materials for these soils are essentially non-vitric. Allophane (Al/Si = 2) has been estimated quantitatively in all soils using oxalate-extractable Si (Si0) and is selected clay fractions using both Si0 and infrared spectroscopy. Maximum concentrations of allophane (Al/Si = 2) range from 5% to 18% of fine earth (< 2 mm) fractions and all occur in B horizons. Fe0 values are low relative to Al0 values except for the upper horizons of the Inceptisol. Al0 values peak in B horizons and the ratio pyrophosphate-extractable Al to Al0 decreases from about 1 in A and upper B horizons to 0.1–0.4 in lower B horizons.An interpretation of the data is consistent with recent proposals that the movement of Al in podzolisation is due primarily to the formation of inorganic complexes with Si. Chemical criteria for spodic horizons should be consistent with the total illuviation of Al and Fe (and perhaps Si), rather than just the organic-bound fraction of Al and Fe in these horizons as indicated by amounts in extractants such as pyrophosphate.  相似文献   

17.
Trace metal behaviour in volcanic ash soils displays distinctive features related to the soils’ large contents of metal‐binding phases and to the rapid release of trace metals from glasses and weatherable minerals. In this work, the BCR (Community Bureau of Reference) sequential extraction scheme (exchangeable + weak acid soluble, reducible, oxidizable, and non‐extractable metal fractions) was applied to selected COST‐622 European reference volcanic soils to determine partitioning of zinc and copper between various solid‐phase constituents, along with the major elements Al, Fe and Mn. The total extracted Al (ΣAl) was strongly correlated with acid ammonium oxalate extractable Al (Alo) (ΣAl = 0.985Alo+ 0.11, R2= 0.98), while the total extracted Fe clearly underestimated the amorphous fraction. Large values for the non‐extractable Al fraction were associated with the presence of gibbsite and phyllosilicates. Although the Zn and Cu contents of the soils were generally large, total amounts extracted (the potentially mobilizable fraction) were small, especially for Zn and for soils with crystalline secondary minerals. The fraction of the total Cu which was potentially mobilizable generally exceeded that of Zn. In the potentially mobilizable Cu the oxidizable fraction was generally dominant. Biocycling appears to play an important role in the surface enrichment of potentially mobilizable Zn and Mn. Although further methodological research seems necessary, the BCR sequential extraction appears to be a valuable tool for studies on metal dynamics in soils with andic properties.  相似文献   

18.
P.M Huang  M.K Wang  M.H Wu  C.L Liu  T.S.C Wang 《Geoderma》1977,18(4):251-263
Twenty two surface soils, representing six parent materials and four soil groups, were sampled in Taiwan for the present study.Except in the soil derived from volcanic ash, the sesquioxidic components and relatively easily extractable Si were present only in small amounts in the NaOAc and H2O2- NaOAc extractable fractions. In addition to Fe, both Si and Al were present in the dithionite-citrate-bicarbonate extracts in considerable amounts, indicating that Si and Al were either present separately or in association with Fe in the sesquioxidic fractions of the soils. The amounts of Si, Al and Fe extracted by the dithionite-citrate-bicarbonate and boiling KOH treatments differed from sample to sample, indicating that they are important variables in the nature of the soils studied.The amounts of the ammonium oxalate-extractable Al and Fe, representing the noncrystalline sesquioxidic products of relatively recent weathering, also differed with parent materials and pedogenic processes. The statistical data indicate that the ammonium oxalate-extractable Al and Fe are related to the contents of organic matter but not to acidity and the contents of clay. The percentage distribution of the extractable Al in the > 2 μm fractions of the selected soil samples ranged from 22.0 to 52.5% and that of the extractable Fe from 11.1 to 38.1%, indicating that the active non-crystalline Al and Fe components in the non-clay fractions deserve close attention in the study of pedogenesis and other soil physicochemical reactions in relation to soil fertility and environmental protection.  相似文献   

19.
H.H. Le Riche 《Geoderma》1973,9(1):43-57
This previously described buried soil, developed in uniform parent material, was used to study the relative movements of elements and other soil components down the profile. Samples from all horizons were treated with hydrogen peroxide and ammonium oxalate, under ultra-violet light, to remove organic matter and sesquioxides, and the residues were subdivided into six particle size fractions.Downward movement of clay (< 0.5 μm) was accompanied by movement of extractable Al2O3 and Fe2O3, thus identifying these as part of the mobile fraction. The less close relationship of extractable Fe2O3 to the clay suggested that it also occurred partly in coarser aggregates. Proportions of minor elements extracted varied from < 1% for Sr to nearly complete extraction of Co, Cu and Mo in some horizons. The extractable fractions of most minor elements throughout the profile behaved more like Fe2O3 than Al2O3. In the extraction residues, nearly all elements were enriched in the clay fractions relative to the coarser fractions; this being greatest for V and Fe.  相似文献   

20.
Abstract

The immobilization of P is a significant fertility limitation of Andisols in Central America. It is believed that soil Al and Fe fractions have an important influence on P availability. This study was conducted to obtain information on the various forms of Al and Fe in ten pedons derived from volcanic ash in Panama and Costa Rica. Correlations between these Al and Fe fractions and P immobilization were measured by different methods.

The Al and Fe fractions, extracted by acid ammonium oxalate, 4M KOH, sodium pyrophosphate and dithionite‐citrate, were determined, and the correlations between these fractions, P immobilization, and other soil properties made.

It was observed that oxalate extractable Al correlated significantly with P immobilization, which had values of over 85% by the New Zealand method and 96% by the isotherm method. The Al concentration corresponding to this immobilization was over 2%. The difference between oxalate extractable Al and pyrophosphate extractable Al (inorganic Al fraction) correlated with P immobilization also. The pyrophosphate extractable Al fraction had the lowest concentrations and did not correlate with P immobilization. The NaF‐pH and dithionite‐citrate extractable Al correlated significantly with P immobilization.

Oxalate extractable Fe correlated with the P retained by the isotherm method, but dithionite‐citrate extractable Fe was negatively correlation with P immobilized. No correlations were found between the pyrophosphate extractable Fe and other soil properties.  相似文献   

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