利用放射性碳对中国变性土的年代确定

Vertisols,which are mainly developed on fluvial and lacustrine deposits and basalt,are extensively distributed in China.66 samples of them for radiocarbon dating were collected across 5 porvinces and 1 autonomous region,ranging from warm-temperate to subtropical and tropical zones in China.The soil organic matter was dated via surface horizon,black soil horizon and dark-colour horizon of the vertisols,whereas carbonate through calcareous concretions and dispersed carbonate in soil profile using radiocarbon method.The present article elucidates the dates of genetic horizons,and of surface and buried vertisols as well.14C dating indicates that the surface vertisols were formed during the end of the late Pleistocene.ca.15600 years ageo.Correlation between depth of sampling and measured 14C age shows that age characteristics of the vertisols of China are close to those of West Germany,Italy,TUrnisia,Australia and Argentina,However,two buried vertisols developed on fluvial and lacustrine deposits were formed during different geological periods,The buried soils in warm-temperate zone were formed in the mid Holocene,while those in subtropics were buried at 12930 years B.P., and formed in the end of the late Pleistocene.     

不同改土物料对白浆土磷吸附解吸的影响

向白浆土各层次土壤施入不同改土物料,比较不同处理土壤对 P 的吸附解吸情况.结果表明:各土层土壤对 P的吸附量均随着平衡液浓度的增加而增加;不同土层间土壤吸附 P 量大小顺序为淀积层＞混拌层＞白浆层＞黑土层;随着平衡液浓度的增大,P 吸附的增加率递减;施 Ca 加大了土壤对 P 的吸附,其中黑土层增加220.16%,白浆层增加54.50%,淀积层增加 52.36%;而施有机肥减弱了土壤对 P 的吸附,其中黑土层降低70.16%,白浆层降低45.50%,淀积层降低55.27%.Ca 有降低土壤 P 解吸率的趋势,有机肥能大幅度地提高其解吸率.     

Characterization of hydrophobic acid fractions in water-soluble organic matter in Dystric Cambisol and in a stream in a small forested watershed: Seasonal and vertical variations in chemical properties

Abstract

Chemical properties of hydrophobic acid (HoA) fractions in water-soluble organic matter in soil and water are concerned with its interactions with mineral soil surfaces and organic pollutants. In 2004 we examined the seasonal and vertical changes in chemical properties of the HoA fraction in a Cambisol profile and compared these properties with those in the HoA fraction of an adjacent stream (aquatic humic substances) in a temperate forested watershed using high performance size exclusion chromatography (HPSEC) and ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy. The HoA fractions from Oi, Oe/Oa, A and B horizon soils in summer had lower O-alkyl C proportions than those recorded in samples in other seasons. The proportions of aromatic C in HoA fractions from A and B horizons were highest in summer. These seasonal variations were less significant than variations with soil depth. O-alkyl C proportions in HoA fractions decreased with increasing soil depth from the Oi to the A horizon. The HoA fractions from the B horizon showed a higher alkyl C proportion than samples from other horizons in winter and spring. These changes with soil depth from the Oi to A horizons might result from selective utilization of carbohydrate carbon by microorganisms, whereas those in the B horizon may result from sorption to mineral surfaces. The HoA fractions in the stream were similar in relative molecular weight, distribution of each type of proton and carbon species in HoA fractions from the B horizon, whereas stream HoA fractions collected in summer would be derived from organic horizons. This indicated that vertical changes in the chemical properties of HoA fractions in soil and pathways of water to the stream would largely affect the chemical properties of HoA fractions in the stream.     

Transport of Phosphorus and Fractionation of Residual Phosphorus in Various Horizons of a Spodosol

The retention and transport of P by three horizon samples (A, E, and Bh) of a Spososol (Oldsmar sand: sandy, silicious, hyperthermic Alfic Arenic Haplaquods) were evaluated using a batch-equilibration and leaching column techniques with application of P in rates equivalent to 25 and 100 kg P ha^-1. Adsorption coefficient (K) values followed the order: Bh > A > E. Adsorption of P by the E horizon soil sample was negligible (M = 4 μg g^-1 soil) as compared to that of either A or Bh horizon samples, e.g., 303 and 479 μg g^-1, respectively. The leaching column study with application of P equivalent to 100 kg ha^-1 showed 39, 68, and 98% of applied P were leached from the Bh, A, and E horizons, respectively, with eight pore volumes of leachate. Elution curves showed the peak P elution at the second pore volume (equivalent to 3.7 cm of water addition). After leaching with eight pore volumes, the residual P in the soil was present primarily in non-occluded Fe and Al-P forms in the A and Bh horizons.     

黄淮海平原晚第四纪古土壤

本文运用孢子花粉,古生物化石和放射性碳断代等手段,从土壤剖面层段的特征,土壤年龄和环境变化方面证明,分布于黄淮海平原的变性土不是现代土壤,而是古土壤,该古土壤自晚新世晚期以来经历了三次沉积－成土作用旋回,其土壤发育程度较弱,且是由钙质结核土层,暗色土层,表土层和（或）淤土层组成的一个叠置型古土壤。     

Mechanisms controlling the mobility of dissolved organic matter, aluminium and iron in podzol B horizons

The processes governing the (im)mobilization of Al, Fe and dissolved organic matter (DOM) in podzols are still subject to debate. In this study we investigated the mechanisms of (im)mobilization of Al, Fe and organic matter in the upper and lower B horizons of two podzols from the Netherlands that are in different stages of development. We equilibrated batches of soil material from each horizon with DOM solutions obtained from the Oh horizon of the corresponding soil profiles. We determined the amount of (im)mobilized Al, Fe and DOM after addition of Al and Fe at pH 4.0 and 4.5 and initial dissolved organic carbon (DOC) concentrations of 10 mg C litre^?1 or 30 mg C litre^?1, respectively. At the combination of pH and DOC concentrations most realistic for the field situation, organic matter was retained in all horizons, the most being retained in the lower B horizon of the well‐developed soil and the least in the upper B horizon of the younger profile. Organic matter solubility seemed to be controlled mainly by precipitation as organo‐metal complexes and/or by adsorption on freshly precipitated solid Al‐ and Fe‐phases. In the lower B horizons, at pH 4.5, solubility of Al and Fe appeared to be controlled mainly by the equilibrium with secondary solid Al‐ and Fe‐phases. In the upper B horizons, the solubility of Al was controlled by adsorption processes, while Fe still precipitated as inorganic complexes as well as organic complexes in spite of the prevailing more acidic pH. Combined with a previous study of eluvial horizons from the same profiles, the results confirm the important role of organic matter in the transport of Al and Fe to create illuvial B horizons initially and subsequently deepening and differentiating them into Bh and Bs horizons.     

Quantifying processes of pedogenesis using optically stimulated luminescence

New analytical techniques have opened up the possibility of addressing rates of soil processes quantitatively. Here, we present the results of an investigation into the use of single‐grain optically stimulated luminescence (OSL) dating to derive rates of soil mixing in the top 50 cm of soil profiles from two toposequences situated in the Werrikimbe National Park in Australia. Of 500 single grains analysed from each sampled depth increment, less than 25% provided a finite age, with the rest of the grains either non‐responsive or dose‐saturated. This proportion of finite‐age grains tended to decrease with soil depth. Median ages of quartz grains increased down the soil profile, with topsoil ages of up to 500 years and subsoil ages of up to 5000 years. Few ‘younger’ grains were found deeper in the profile and few ‘older’ grains near the soil surface. These trends suggest that pedoturbation is resulting in vertical transport of grains through the profile, but that there is a distribution of transport distances, with a poor probability of large transport distances from surface to subsoil or vice versa compared with a more frequent movement of grains to and from the surface in the uppermost 10–35 cm. The calculation of a single age for each soil horizon was unachievable as each horizon contained a heterogeneous mixture of grains with varying histories of transport to and from the soil surface. Soil mixing was confirmed along both toposequences studied. However, the occurrence of minor mixing rates did not lead to a homogenization of the topsoil and adjacent horizons. We postulated that mixing velocities were mostly related to flora at our study site. Vertical soil mixing rates of 0.5 and 0.2 mm year^?1 were calculated from the distribution of finite single‐grain ages.     

Soil formation in the coast aeolianites and sands of Natal

The morphological, physical, chemical and mineralogical properties of eight prominent classes of soil developed in the coast aeolianites and sands of Natal are presented. These data and information on soil geography lead to the conclusion that: (i) losses of silica and bases and relative accumulation of iron (the ferrallitic process) have given rise to red and yellow kaolinitic materials; (ii) clay eluviation has given rise to coarse textured topsoils and to B2t horizons; and (iii) the hydromorphic process has caused grey colours in many sandy topsoils, plinthite development at some E/B horizon interfaces and gleying of some B2 horizons. In the soils on the older aeolianites, there is no evidence of either podzolization or the coarser textured topsoil being a younger geological deposit. The development of yellow soils in younger aeolianites may indicate a cooler climate than existed when red materials developed from the older aeolianites.     

Comparison of 0.1N sodium hydroxide with 0.1M sodium pyrophosphate in the extraction of soil organic matter from various soil horizons

Abstract

Soil samples representing the O, A, B, and C soil horizons from soil organic matter (SOM) studies were selected to study the relative effectiveness of 0.1N sodium hydroxide (NaOH) and 0.1M sodium pyrophosphate (NaPyr) in extracting organic carbon (OC). Replicate samples were extracted with each extractant in a ratio of about 1:144 and successive extractions were performed for each soil. Results indicated the importance of successive extractions for more complete removal of extractable OC. A single extraction removed an average of only 68%, 78%, 86%, and 60% of the OC extracted with four successive extractions for the O, A, B, and C horizons, respectively. The C horizons were lowest in OC and the slowest to release OC in the extraction process. Organic C was solubilized from the B horizons most quickly with an average of 95% of the successively extractable OC removed with only two extractions. The extractability of the soil TOC was highest in the Bhs and then the Bw, C, A, and O horizons at 92% and 42%, 46%, 38%, and 3 6%, respectively. The NaOH and NaPyr were nearly equal in extracting OC from the Bhs horizons. The NaOH extracted more OC than the NaPyr at 53%, 55%, 29%, and 47% more in the O, A, Bw, and C horizon samples, respectively. These results stress the importance of considering the soil horizon type and the use of NaOH in successive extraction for maximum removal of OC in soil studies.     

Podzol formation in sandy soils of Finland

Podzolization occurs quickly in acidic parent materials with addition of acidic litter from coniferous trees. This study was conducted to evaluate Podzol formation and estimate lengths of time required to meet morphological and chemical criteria of podzolic B horizon and spodic horizon in Finland. Soil color, organic C, ODOE, and extractable Al and Fe were measured in a seven-pedon chronosequence (230–1800 years) and four older pedons (8300–11,300 years). The bulk mineralogical composition of the BC and C horizons was uniform with quartz, plagioclase and K-feldspar as main components and amphibole, illite and chlorite as minor components. The fine (<5 μm) fraction of selected samples was primarily amorphous allophone-like material with some mixed-layered illite–vermiculite. All pedons in the study met the criteria for albic horizons according to the FAO–Unesco, World Reference Base (WRB) and Soil Taxonomy systems. According to the FAO–Unesco system, all pedons had spodic B horizons and were classified as Podzols. According to the WRB system, none of pedons of the chronosequence had spodic horizons, whereas the older pedons met the criteria for a spodic horizon. About 4780 years were required to form a spodic horizon according to the WRB system. The oldest pedon of the chronosequence and the older pedons had spodic horizons according to Soil Taxonomy, but the younger pedons failed to meet the spodic horizon criteria. About 1520 years were required to form a spodic horizon that met the color and organic C criteria of Soil Taxonomy, whereas it took about 4780 years to meet the required accumulation of Fe and Al. This study points out the discrepancy between the color criteria and the criteria reflecting the accumulation of Al, Fe and organic matter in the B horizon.     

31Phosphorus‐Nuclear magnetic resonance analysis in extracts of a phosphorus‐enriched volcanic soil of Chile

Abstract

The nature of organic and inorganic phosphorus (P) in fertilized and unfertilized samples of Vilcun soil, a Chilean medial mesic typic Dystrandept which was studied through ³¹phosphorus‐nuclear magnetic resonance (³¹P‐NMR) analysis carried out on a single alkaline extraction. The total P contents ranged from 1,506 mg P kg^‐1 (B horizon, unfertilized soil) to 7,541 mg P kg^‐1 (A horizon, fertilized soil). The magnitude of the P signal (SEM‐EDAX results) appears to be related to that of the iron (Fe) signal. Signals of ³¹P‐NMR spectra are attributable to inorganic orthophosphate, and orthophosphate monoesters and diesters. No important differences between horizons were observed. Apparently in this soil, P are mainly associated with iron oxides and organic matter. The organic P forms were not readily subjected to mineralization.     

南极Fildes半岛成土过程中主要元素的行为

Nine horizon samples of three soil profiles representative of Dystri-gelic Cambisol, Fibri-gelic Histosol and Relic Ornithosol were taken from Fildes Peninsula of King George Island, South Shetland Islands to quantitatively demonstrate the enrichment, migration and loss of the elements (Si, Al, Fe, Ca, Mg, Mn, K, Na and P) in soil horizons and their behaviour within profiles by application of the enrichment coefficient calculated in terms of the abundance of Ti. Six horizon samples of 4 other profiles randomly taken from the studied area were examined for calculation of the redistributing enrichment coefficient, which was applied for a better understanding of the element redistribution between soil and clay fraction along with soil development. The results showed that the enrichment, migration and redistribution of the elements varied strongly among the investigated soils and horizons, due to the differences of weathering degrees and moisture status, influences of sea bird activities, etc.     

Crop use and profile distribution of phosphorus in soils that developed on mafic rocks in southern Portugal

The phytoavailability of soil phosphorus (P) depends on the different forms in which it occurs and how these forms change after the application of P fertiliser to the soil. Forms of P in the A, B and C horizons of eleven pedons that developed on mafic rocks were characterised by a fractionation method before and after fertilisation with single superphosphate, and a micropot experiment was conducted to assess the short-term use of P fertiliser by rye (Secale cereale L.). The main sources of P to the crop were (i) phosphate adsorbed on mineral surfaces and pedogenic Fe, Al or Ca phosphates in the A horizon and (ii) Ca-phosphates in B and C horizons. In the C horizons, poor in Fe/Al phases and clay, the precipitated Ca-P showed low solubility, resulting in a reduction in shoot biomass. The apparent P recovery by rye was similar in the A (36%) and B (29%) but decreased in the C (15%) horizons. The partial factor productivity (g g^?1) decreased from the A (58) to B (11) and C (5) horizons. P phytoavailability decreased with increasing profile depth because the transformation of P fertiliser to poorly soluble Ca-P forms increased with depth.     

Soil heterogeneity and profile development in a stratified gravel deposit in Ireland

The spatial variation in a soil section developed in a stratified, coarse-textured deltaic deposit is documented. Analytical and morphological data are presented for 8 A horizon, 19 B horizon and 6 C horizon samples taken from a 5-m section. The occurrence of a lithologic discontinuity at the A-B boundary as well as many stratigraphical discontinuities occurring diagonally across the B and C horizons is demonstrated. As a consequence a number of different soil profiles, which would place the soils in diverse soil orders or great groups in most classification systems, were found to exist side by side in the section studied. The problem of placing lateral boundaries to sampling sites in such materials is highlighted and the exclusive use of fine earth (<2 mm material) when assessing pedogenic trends and processes in coarse-textured materials is questioned.     

Studies on the properties of organic matter in buried humic horizon derived from volcanic ash

To investigate the relationship between age and the sugar composition in hydrolysates of the surface horizon and buried humic horizons with age up to 28,000 years B.P., the neutral sugars and amino sugars in soil hydrolysates were determined.

The ratios of total sugar carbon content to total carbon content of soil ranged from 2.68 to 4.13 percent. These values showed no distinct relationship with age.

Rhamnose, fucose, arabinose, xylose, mannose, galactose, glucose, g1ucosamine and galactosamine were present in the hydrolysates of all soil samples.

The polysaccharides of soil samples which have been buried for shorter periods were dominated by glucose, while those of soil samples buried for longer periods were dominated by mannose.

The proportion of hexoses showed a tendency to increase with age, while that of pentoses showed a tendency to decrease with age.     

Phosphatase activity in the surface and buried chestnut soils of the Volga-Don interfluve

The phosphatase activity (PA) was studied in the chestnut paleosols buried in 1718–1720 under the Anna Ivanovna rampart in the southern part of the Privolzhskaya Upland and in the middle of the third millennium BC under the burial mound of the Bronze Age on the Northern Yergeni Upland; the background analogues of these soils were also examined. The PA values in the fresh soil samples varied from 2.5 to 37 mg of P₂O₅/10 g of soil per h with maximums in the A1 horizon of the surface soils and in the B1 horizon of the paleosols. The PA values depended on the time of storage of the samples: with time, they increased by 2.6–2.9 times in the A1 horizon of the background surface soil and decreased by 20–60% in the other soil samples. The specific distribution patterns of the PA values in the soil profiles remained the same independently of the time of storage of the samples. Relatively small amounts of the soil samples were sufficient for the reliable determination of the PA: 1–2 g for the A1 horizon and 3–5 g for the B1 and B2 horizons. The time of incubation with the substrate had to be increased up to 4 h for the long-stored samples.     

Genesis of a Xeralf on feldspathic sandstone, South Australia

A Xeralf on feldspathic sandstone was sampled from a hillslope in the Mount Lofty Ranges in order to study its genesis and, in particular, the origin of the strong texture contrast. Micromorphological study demonstrated that the clay present in void argillans and papules in the B2 horizon accounted for only a small amount of the clay present. Elemental analysis of the whole soil (< 2 mm) and sand, silt and clay fractions showed that there had been considerable weathering of both quartz and microcline, which were the dominant minerals present. Kaolinite is the dominant clay mineral weathering product. Illite appears to be forming from vermiculite in the A horizon. Using zircon as an internal standard, it was shown that elemental losses of SiO₂ and reductions in weight and volume were similar in A and B horizons. Losses of aluminium and potassium were greatest in the A horizon, least in the B3. There has been an absolute increase in the amount of iron. A possible source is iron from heavy mineral bands upslope. It was concluded from the similarity of the quartz particle-size distributions of the A2, B2 and B3 horizons that the intensity of weathering of quartz was the same in A and B horizons. In the case of feldspar (mostly microcline), there is a greater proportion of feldspar in the fine sand and silt fractions of the A2 horizon than in the B horizon. Weathering of feldspar is greatest in the A horizon. The texture profile is principally a function of greater lateral loss of clay from the A horizons compared to the B horizons.     

Vertical distribution of soil properties under short‐rotation forestry in Northern Germany

Short‐rotation forestry (SRF) on arable soils has high potentials for biomass production and leads to long‐term no‐tillage management. In the present study, the vertical distributions of soil chemical and microbial properties after 15 y of SRF with willows and poplar (Salix and Populus spp.) in 3‐ and 6‐year rotations on an arable soil were measured and compared to a pertinent tilled arable site. Two transects at different positions in the relief (upper and lower slope; transect 1 and 2) were investigated. Short‐rotation forestry caused significant changes in the vertical distribution of all investigated soil properties (organic and microbial C, total and microbial N, soil enzyme activities), however, the dimension and location (horizons) of significant effects varied. The rotation periods affected the vertical distribution of the soil properties within the SRF significantly. In transect 1, SRF had higher organic‐C concentrations in the subsoil (Bv horizon), whereas in transect 2, the organic‐C concentrations were increased predominantly in the topsoil (Ah horizon). Sufficient plant supply of P and K in combination with decreased concentrations of these elements in the subsoil under SRF pointed to an effective nutrient mobilization and transfer from the deeper soil horizons even in the long term. In transect 1, the microbial‐C concentrations were higher in the B and C horizons and in transect 2 in the A horizons under SRF than under arable use. The activities of β‐glucosidases and acid phosphatases in the soil were predominantly lower under SRF than under arable use in the topsoil and subsoil. We conclude, that long‐term SRF on arable sites can contribute to increased C sequestration and changes in the vertical distribution of soil microbial biomass and soil enzyme activities in the topsoil and also in the subsoil.     

Alkyl C and hydrophobicity in B and C horizons of an acid forest soil

Aliphatic C most probably derived from ester‐bound moieties was found to be present in sandy subsoil horizons. The hydrophobic nature of such compounds may increase their stabilization potential. Therefore, the aim of this study was to investigate the potential of aliphatic compounds in mineral soil horizons along a Dystric Cambisol profile under beech forest to increase hydrophobicity. The conceptual approach included the analyses of soil samples before and after solvent extraction and base hydrolysis for elemental and isotopic composition. Additionally, the advancing contact angle was measured to quantify hydrophobicity. Curie‐point pyrolysis GC/MS was carried out to characterize the nature of alkyl C present in subsoil samples. A close correlation between the ¹⁴C activity and the stable‐C‐isotope ratio (δ¹³C) indicates isotopic fractionation upon C stabilization in subsoils. Free lipids contributed less than 10% to the organic C found in subsoil horizons. Base hydrolysis revealed very high amounts of hydroxyalkanoic acids in the B horizons of the acid forest soil. Hydrophobicity of SOM was not found to be correlated to esterified‐ or free‐lipid content. The contact angle was in a similar range for all bulk soil horizons, suggesting greater hydrophobicity of organic matter in subsoil horizons considering their very low concentrations of organic C compared to the A horizon. The quantity and nature of pyrolysis products change with increasing depth in the soil profile. Aliphatic products cannot be detected in B and C horizons by Curie‐point pyrolysis GC/MS.     

Spatial and temporal variation in podzol organic matter studied by pyrolysis-gas chromatography/mass spectrometry and micromorphology

A well‐developed podzol hydrosequence that has been partially covered with drift sand, and partially subjected to improved drainage, provides new insights into the causes of variation in soil organic matter chemistry in such soils. While E horizons invariably move towards a dominance of aliphatic components reflecting residual accumulation, the chemistry of organic matter in well‐drained B horizons is determined mainly by decaying roots, which are transformed by microorganisms to humus aggregates. In poorly drained, stratified B horizons, humus coatings dominate and the chemistry is very close to that of dissolved organic carbon. When a sand cover inhibits the supply of fresh litter, microbial decomposition in the A horizon causes a shift in chemistry towards that of the E horizon. Similarly, upon improved drainage and removal of complexed metals from the top of the B horizon, microbial decomposition of all palatable organic matter in the top of the B horizon causes a shift towards E‐horizon chemistry. This is probably the mechanism by which most E horizons in podzols are formed, and not by re‐solution. Marked chemical changes upon improved drainage may take only decades. During microbial decay, small polysaccharide‐derived pyrolysis products (mainly furans, furaldehydes and acetic acid) remain abundant due to the contribution of microbial sugars. Both micromorphology and factor analysis on quantified results of pyrolysis‐gas chromatography/mass spectrometry contribute significantly to the interpretation of the humus chemistry of these profiles and thus to our understanding of soil genesis. Organic chemistry of the investigated podzols can be understood only in the context of their genesis.