Cold and hot water–extractable organic matter as indicators of litter decomposition in forest soils

Mild extractions were used as indicators of easily decomposable organic matter (OM). However, the chemical composition of extracted OM often remained unclear. Therefore, the composition of cold and hot water–extractable OM was investigated in the O horizons (Oi, Oe, Oa) of a 170 y old beech stand (Fagus sylvatica) in the Ore Mtns., SE Germany. To simulate litter decomposition, the O horizon samples were incubated for 1 week under defined conditions. Cold‐ and hot‐water extracts were analyzed and chemically characterized by pyrolysis–field ionization mass spectrometry (Py‐FIMS). The C and N concentrations were always lower in the cold‐(C: 2.69 to 3.95 g kg^–1; N: 0.14 to 0.29 g kg^–1) than in the hot‐water extracts (C: 13.77 to 15.51 g kg^–1; N: 0.34 to 0.83 g kg^–1). The C : N ratios of both extracts increased with increasing depth. Incubation increased the concentrations of C and N in all water extracts, while C : N ratios of extracts decreased. The molecular‐chemical composition of cold and hot water–extracted OM revealed distinct differences. Generally, cold water–extracted OM was thermally more stable than hot water–extracted OM. The mass spectra of the hot water–extracted organic matter revealed more intensive signals of carbohydrates, phenols, and lignin monomers. Additionally, the n‐C₂₈ fatty acid and the n‐C₃₈–to–n‐C₅₂ alkyl monoesters clearly distinguished the hot‐ from the cold‐water extract. A principle‐component analysis visualized (1) alterations in the molecular‐chemical composition of cold‐ and hot‐water extracts due to previous incubation of the solid O horizon samples and (2) a decomposition from the Oi to the Oh horizon. This provides evidence that the macromorphological litter decomposition was reflected by the chemical composition of water extracts, and that Py‐FIMS is well‐suited to explain at the molecular level why OM decomposability is correlated with water‐extracted C.     

Soil organic matter stabilization in acidic forest soils is preferential and soil type-specific

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 (Fe_o; Al_o), and dithionite‐extractable Fe (Fe_d) 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 Al_o and Fe_o results in a particularly stable and relatively old C pool, which is potentially stable for thousands of years.     

Paddy management on different soil types does not promote lignin accumulation

Paddy soil management is generally thought to promote the accumulation of soil organic matter (SOM) and specifically lignin. Lignin is considered particularly susceptible to accumulation under these circumstances because of the recalcitrance of its aromatic structure to biodegradation under anaerobic conditions (i.e ., during inundation of paddy fields). The present study investigates the effect of paddy soil management on SOM composition in comparison to nearby agricultural soils that are not used for rice production (non‐paddy soils). Soil types typically used for rice cultivation were selected, including Alisol, Andosol and Vertisol sites in Indonesia (humid tropical climate of Java) and an Alisol site in China (humid subtropical climate, Jiangxi province). These soil types represent a range of soil properties to be expected in Asian paddy fields. All upper‐most A horizons were analysed for their SOM composition by solid‐state ¹³C nuclear magnetic resonance (NMR) spectroscopy and for lignin‐derived phenols by the CuO oxidation method. The SOM composition was similar for all of the above named parent soil types (non‐paddy soils) and was also not affected by paddy soil management. A substantial proportion (up to 23%) of the total aryl‐carbon in some paddy and non‐paddy soils was found to originate from condensed aromatic‐carbon (e.g ., charcoal). This may be attributed to the burning of crop residues. On average, the proportion of lignin was low and made up 20% of the total SOM, and showed no differences between straw, particulate organic matter (POM), and the bulk soil material. The results from CuO oxidation are consistent with the data obtained from solid‐state ¹³C NMR spectroscopy. The extraction of lignin‐derived phenols revealed low VSC (vanillyl, syringyl, cinnamyl) values for all investigated soils in a range (4 to 12 g kg⁻¹ OC) that was typical for agricultural soils. In comparison to adjacent non‐paddy soils, the data do not provide evidence for a substantial accumulation of phenolic lignin‐derived structures in the paddy soils, even for those characterized by higher organic carbon (OC) contents (e.g ., Andosol‐ and Alisol (China)‐derived paddy soils). We conclude that the properties of the parent soil types are more important for the lignin content of the soils than the effect of paddy management itself.     

Klimaeinfluß auf Lignin und Polysaccharide in Partikelgrößen-Fraktionen zonaler Steppenböden Rußlands

Climatic effect on lignin and polysaccharides in particle-size fractions of zonal steppe soils, Russia Zonal soils derived from similar parent materials are suitable for investigating the question, whether and how climate affects soil organic matter properties. For this reason we sampled 10 native surface (0—10 cm) and subsurface (ca. 50—60 cm) soil horizons in the native steppe and forest steppe of Russia. Polysaccharides and the vanillyl, syringyl and cinnamyl structural units of lignin (VSC) were determined in the fine earth (< 2 mm) as well as in clay (< 2 μm) and silt (2—20 μm) fractions. As the ratio of mean annual precipitation to potential evaporation (N/V) decreased, the concentrations of polysaccharides tended to decrease in the subsoil horizons. This was indicated most clearly for the silt fractions (r = 0.98**). In contrast, the VSC contents (in g kg^—1 organic C) of the subsoils increased as N/V decreased (r = —0.92*), resulting in increasing VSC/polysaccharide ratios of the subsoil horizons with decreasing N/V ratio (r = —0.94*). It is suggested that production of polysaccharides or their transport into the mineral subsoil or both is favored at sites with wide rather than narrow N/V ratio, whereas lignin might be selectively enriched during intense soil organic matter decay at the Southern sites.     

Soil properties and tree growth along an altitudinal transect in Ecuadorian tropical montane forest

In tropical montane forests, soil properties change with increasing altitude, and tree‐growth decreases. In a tropical montane forest in Ecuador, we determined soil and tree properties along an altitudinal transect between 1960 and 2450 m asl. In different vegetation units, all horizons of three replicate profiles at each of eight sites were sampled and height, basal area, and diameter growth of trees were recorded. We determined pH and total concentrations of Al, C, Ca, K, Mg, Mn, N, Na, P, S, Zn, polyphenols, and lignin in all soil horizons and in the mineral soil additionally the effective cation‐exchange capacity (CEC). The soils were Cambisols, Planosols, and Histosols. The concentrations of Mg, Mn, N, P, and S in the O horizons and of Al, C, and all nutrients except Ca in the A horizons correlated significantly negatively with altitude. The C : N, C : P, and C : S ratios increased, and the lignin concentrations decreased in O and A horizons with increasing altitude. Forest stature, tree basal area, and tree growth decreased with altitude. An ANOVA analysis indicated that macronutrients (e.g., N, P, Ca) and micronutrients (e.g., Mn) in the O layer and in the soil mineral A horizon were correlated with tree growth. Furthermore, lignin concentrations in the O layer and the C : N ratio in soil affected tree growth. These effects were consistent, even if the effect of altitude was accounted for in a hierarchical statistical model. This suggests a contribution of nutrient deficiencies to reduced tree growth possibly caused by reduced organic‐matter turnover at higher altitudes.     

Organic matter in particle-size fractions from A and B horizons of a Haplic Alisol

The organic matter in soils may be stabilized by its interactions with minerals. We have studied such interactions in a Haplic Alisol under forest in which clay and organic matter have migrated from an eluvial A horizon to accumulate in an illuvial B horizon. We have tried to trace the fate of organic matter in these horizons (Ah and Bvt) by determining clay mineralogy, carbon and nitrogen content, hydrolysable amino acids, lignin signature by alkaline CuO oxidation and carbon species by ¹³C CPMAS NMR of bulk soils and particle‐size fractions. In both horizons, most of the organic matter was present in O–alkyl and methylene structures, each contributing one‐third to the bulk organic matter. In the Ah horizon the ratios of carbon‐to‐nitrogen, and yields for lignin and hydrolysable amino acids decreased as the particle‐size class decreased, but side‐chain oxidation of lignin compounds increased with decreasing particle size. In contrast to previous observations, the proportions of O–alkyl carbon increased as particle size decreased, constituting a major proportion of the organic carbon in the clay‐size fractions from both the Ah and Bvt horizons (≥ 38%), while proportions of methylene carbon decreased. Illite was the dominant mineral in the fraction ≤ 6 μm, whereas the mobile fine clay fraction (<0.2 μm) was rich in smectites – minerals with large surface areas. Our results support the hypothesis that potentially labile organic matter, such as O–alkyl carbon typically present in polysaccharides, may be stabilized against further degradation in organomineral complexes.     

Distribution of Organic Carbon in the Humic Fractions of Diagnostic Horizons from Brazilian Soils

Abstract

This study was developed on 52 soil profiles, 61 surface diagnostic horizons, and 26 subsurface diagnostic horizons classified according to the Soil Taxonomy and Brazilian Soil Classification System (SiBCS) as Mollisols (Chernossolos), Spodosols (Espodossolos), Entisols (Gleissolos), Oxisols (Latossolos), and Histosols (Organossolos). The objective was to quantify the carbon (C) in organic matter fractions and to correlate it with soil chemical attributes. Soil organic matter was fractionated into fulvic acids (C‐FAF), humic acids (C‐HAF), and humin (C‐HUM), and the ratios C‐HAF/C‐FAF and AE (alkaline extract)/C‐HUM were calculated. Humin was the predominant fraction in Mollisols and Oxisols, which showed values of AE/C‐HUM and C‐HAF/C‐FAF lower than 1.0. The humin fraction was also predominant in surface horizons of Spodosols and Entisols, whereas a higher content of C‐FAF and C‐FAH was observed in the subsurface horizons, with values higher than 1.5 for the AE/C‐HUM ratio. C‐HAF was predominant in the Histosols, and C‐HAF/C‐FAF ratio values were higher than 2.0. The highest correlation values with soil attributes were observed for C‐HAF, C‐HUM, and total organic C with pH, sum of bases, and cation exchange capacity. The differences in humic substances distribution was a useful parameter to characterize soil orders in the Brazilian soil classification system and to understand pedogenic processes.     

Content and composition of free and occluded particulate organic matter in a differently textured arable Cambisol as revealed by solid‐state 13C NMR spectroscopy

The composition of functional light soil organic matter pools of arable Cambisols with a gradient in clay content was investigated. Soil texture differences originate from increasing loess admixture to the parent material (coarse‐grained tertiary sediments). Using density fractionation in combination with ultrasonic dispersion, two types of particulate organic matter (POM) were obtained: (1) free POM and (2) POM occluded in soil aggregates. Both POM fractions were analyzed by elemental analysis (C, N) and CPMAS ¹³C NMR spectroscopy. With increasing clay content the amount of organic carbon stored in the occluded POM fraction increased considerably, whereas the amounts of free POM were not related to the soil clay content. With increasing soil clay contents increasing proportions of O‐alkyl C and decreasing proportions of aryl C were found for both POM fractions. The occluded POM fraction showed a higher degree of degradation as indicated by lower amounts in O‐alkyl carbon. A lower degree of POM degradation was associated with higher clay contents. Higher soil clay contents promoted the conservation of POM with a low degree of alteration. This effect of soil texture was found to be highly significant when the aryl C : O‐alkyl C ratio was used as indicator for POM decomposition rather than the alkyl C : O‐alkyl C ratio.     

Carbon and nitrogen isotope composition of bulk soils, particle-size fractions and organic material after treatment with hydrofluoric acid

Soils and sediments contain only small amounts of organic matter, and large concentrations of paramagnetic metals can give poor solid‐state nuclear magnetic resonance (NMR) spectra of organic matter. Pretreatment of samples with hydrofluoric acid (HF) dissolves significant proportions of the mineral matrix and extracts paramagnetic elements. We investigated the effects of 10% HF treatment on the stable isotope content of carbon (C) and nitrogen (N) of organic matter from soils, composts and shales. Additionally we inferred molecular and isotopic characteristics of lost materials from calculations of isotope mass balances. Treatment with HF enriched C and N in mineral samples substantially (factors 2.5–42.4), except for Podzol B horizons (1.1–1.7) and organic material (1.0–1.3). After treatment most of the C (59.7–91.7%) and N (53.7–86.6%) was recovered, although changing C/N ratios often indicated a preferential loss of N‐rich material. Isotope ratios of C and N in the remaining material became more negative when net alterations exceeded 0.3‰. The isotope ratios of the lost material contained more ¹³C (1–2‰) and ¹⁵N (1–4‰) than the initial organic matter. Acid hydrolysis typically removes proteins, amino acids and polysaccharides, all of which are enriched in ¹³C, and in the case of proteins and amino acids, enriched in ¹⁵N as well. We conclude that HF treatment released fresh, soluble, probably microbial, biomass in addition to carbohydrates. Net changes of the bulk chemical composition of organic matter were small for most soils, size fractions and plant material, but not for samples containing little organic matter, or those rich in easily soluble organic matter associated with iron oxides, such as Podzol B horizons.     

Soil microbial biomass and activity: the effect of site characteristics in humid temperate forest ecosystems

Microbial biomass, respiratory activity, and in‐situ substrate decomposition were studied in soils from humid temperate forest ecosystems in SW Germany. The sites cover a wide range of abiotic soil and climatic properties. Microbial biomass and respiration were related to both soil dry mass in individual horizons and to the soil volume in the top 25 cm. Soil microbial properties covered the following ranges: soil microbial biomass: 20 µg C g^–1–8.3 mg C g^–1 and 14–249 g C m^–2, respectively; microbial C–to–total organic C ratio: 0.1%–3.6%; soil respiration: 109–963 mg CO₂‐C m^–2 h^–1; metabolic quotient (qCO₂): 1.4–14.7 mg C (g C_mic)^–1 h^–1; daily in‐situ substrate decomposition rate: 0.17%–2.3%. The main abiotic properties affecting concentrations of microbial biomass differed between forest‐floor/organic horizons and mineral horizons. Whereas microbial biomass decreased with increasing soil moisture and altitude in the forest‐floor/organic horizons, it increased with increasing N_tot content and pH value in the mineral horizons. Quantities of microbial biomass in forest soils appear to be mainly controlled by the quality of the soil organic matter (SOM), i.e., by its C : N ratio, the quantity of N_tot, the soil pH, and also showed an optimum relationship with increasing soil moisture conditions. The ratio of C_mic to C_org was a good indicator of SOM quality. The quality of the SOM (C : N ratio) and soil pH appear to be crucial for the incorporation of C into microbial tissue. The data and functional relations between microbial and abiotic variables from this study provide the basis for a valuation scheme for the function of soils to serve as a habitat for microorganisms.     

Long‐term fertilization and manuring effects on physically separated soil organic‐matter pools under continuous wheat cropping at a rainfed semiarid site in China

An essential prerequisite for a sustainable soil use is to maintain a satisfactory soil organic‐matter (OM) level. This might be achieved by sound fertilization management, though impacts of fertilization on OM have been rarely investigated with the aid of physical fractionation techniques in semiarid regions. This study aimed at examining changes in organic C (OC) and N concentrations of physically separated soil OM pools after 26 y of fertilization at a site of the semiarid Loess Plateau in China. To separate sensitive OM pools, total macro‐OM (> 0.05 mm) was obtained from bulk soil by wet‐sieving and then separated into light macro‐OM (< 1.8 g cm^–3) and heavy macro‐OM (> 1.8 g cm^–3) subfractions; bulk soil was also differentiated into light OM (< 1.8 g cm^–3) and mineral‐associated OM (> 1.8 g cm^–3). Farmyard manure increased concentrations of total macro‐OC and N by 19% and 25%, and those of light fraction OC and N by 36% and 46%, compared to no manuring; both light OC and N concentrations but only total macro‐OC concentration responded positively to mineral fertilizations compared to no mineral fertilization. This demonstrated that the light‐fraction OM was more sensitive to organic or inorganic fertilization than the total macro‐OM. Mineral‐associated OC and N concentrations also increased by manuring or mineral fertilizations, indicating an increase of stable OM relative to no fertilization treatment, however, their shares on bulk soil OC and N decreased. Mineral fertilizations improved soil OM quality by decreasing C : N ratio in the light OM fraction whereas manuring led to a decline of the C : N ratio in the total macro‐OM fraction, with respect to nil treatment. Further fractionation of the total macro‐OM according to density clarified that across treatments about 3/4 of total macro‐OM was associated with minerals. Thus, by simultaneously applying particle‐size and density separation procedures, we clearly demonstrated that the macro‐OM differed from the light OM fraction not only in its chemical composition but also in associations with minerals. The proportion of the 0.5–0.25 mm water‐stable aggregates of soil was higher under organic or inorganic fertilizations than under no manure or no mineral fertilization, and increases in OC and N concentrations of water‐stable aggregates as affected by fertilization were greater for 1–0.5 and 0.5–0.25 mm classes than for the other classes. Results indicate that OM stocks in different soil pools can be increased and the loose aggregation of these strongly eroded loess soils can be improved by organic or inorganic fertilization.     

Changes in soil organic matter composition are associated with forest encroachment into grassland with long-term fire history

This study investigates if Araucaria forest (C₃ metabolism) expansion on frequently burnt grassland (C₄ metabolism) in the southern Brazilian highland is linked to the chemical composition of soil organic matter (SOM) in non‐allophanic Andosols. We used the ¹³C/¹²C isotopic signature to group heavy organo‐mineral fractions according to source vegetation and ¹³C NMR spectroscopy, lignin analyses (CuO oxidation) and measurement of soil colour lightness to characterize their chemical compositions. Large proportions of aromatic carbon (C) combined with small contents of lignin‐derived phenols in the heavy fractions of grassland soils and grass‐derived lower horizons of Araucaria forest soils indicate the presence of charred grass residues in SOM. The contribution of this material may have led to the unusual increase in C/N ratios with depth in burnt grassland soils and to the differentiation of C₃‐ and C₄‐derived SOM, because heavy fractions from unburnt Araucaria forest and shrubland soils have smaller proportions of aromatic C, smaller C/N ratios and are paler compared with those with C₄ signatures. We found that lignins are not applicable as biomarkers for plant origin in these soils with small contents of strongly degraded and modified lignins as the plant‐specific lignin patterns are absent in heavy fractions. In contrast, the characteristic contents of alkyl C and O/N‐alkyl C of C₃ trees or shrubs and C₄ grasses are reflected in the heavy fractions. They show consistent changes of the (alkyl C)/(O/N‐alkyl C) ratio and the ¹³C/¹²C isotopic signature with soil depth, indicating their association with C₄ and C₃ vegetation origin. This study demonstrates that soils may preserve organic matter components from earlier vegetation and land‐use, indicating that the knowledge of past vegetation covers is necessary to interpret SOM composition.     

Dissolved organic matter sorption by mineral constituents of subsoil clay fractions

The retention of dissolved organic matter in soils is mainly attributed to interactions with the clay fraction. Yet, it is unclear to which extent certain clay‐sized soil constituents contribute to the sorption of dissolved organic matter. In order to identify the mineral constituents controlling the sorption of dissolved organic matter, we carried out experiments on bulk samples and differently pretreated clay‐size separates (untreated, organic matter oxidation with H₂O₂, and organic matter oxidation with H₂O₂ + extraction of Al and Fe oxides) from subsoil horizons of four Inceptisols and one Alfisol. The untreated clay separates of the subsoils sorbed 85 to 95% of the dissolved organic matter the whole soil sorbed. The sorption of the clay fraction increased when indigenous organic matter was oxidized by H₂O₂. Subsequent extraction of Al and Fe oxides/hydroxides caused a sharp decrease of the sorption of dissolved organic matter. This indicated that these oxides/hydroxides in the clay fraction were the main sorbents of dissolved organic matter of the investigated soils. Moreover, the coverage of these sorbents with organic matter reduced the amount of binding sites available for further sorption. The non‐expandable layer silicates, which dominated the investigated clay fractions, exhibited a weak sorption of dissolved organic matter. Whole soils and untreated clay fractions favored the sorption of ”︁hydrophobic” dissolved organic matter. The removal of oxides/hydroxides reduced the sorption of the lignin‐derived ”︁hydrophobic” dissolved organic matter onto the remaining layer silicates stronger than that of ”︁hydrophilic” dissolved organic matter.     

Changes in the chemical composition of soil organic matter after application of compost

Is the composition of soil organic matter changed by adding compost? To find out we incubated biowaste composts with agricultural soils and a humus‐free mineral substrate at 5°C and 14°C for 18 months and examined the products. Organic matter composition was characterized by CuO oxidation of lignin, hydrolysis of cellulosic and non‐cellulosic polysaccharides (CPS and NCPS) and ¹³C cross‐polarization magic angle spinning nuclear magnetic resonance (CPMAS ¹³C‐NMR) spectroscopy. The lignin contents in the compost‐amended soils increased because the composts contained more lignin, which altered little even after prolonged decomposition of the composts in soil. A pronounced decrease in lignin occurred in the soils amended with mature compost only. Polysaccharide C accounted for 14–20% of the organic carbon at the beginning of the experiment for both the compost‐amended soils and the controls. During the incubation, the relative contents of total polysaccharides decreased for 9–20% (controls) and for 20–49% (compost‐amended soils). They contributed preferentially to the decomposition as compared with the bulk soil organic matter, that decreased between < 2% and 20%. In the compost‐amended agricultural soils, cellulosic polysaccharides were decomposed in preference to non‐cellulosic ones. The NMR spectra of the compost‐amended soils had more intense signals of O–alkyl and aromatic C than did those of the controls. Incubation for 18 months resulted mainly in a decline of O–alkyl C for all soils. The composition of the soil organic matter after compost amendment changed mainly by increases in the lignin and aromatic C of the composts, and compost‐derived polysaccharides were mineralized preferentially. The results suggest that decomposition of the added composts in soil is as an ongoing humification process of the composts themselves. The different soil materials affected the changes in soil organic matter composition to only a minor degree.     

Long‐term effects of liming on microbial biomass and activity and soil organic matter quality (13C CPMAS NMR) in organic horizons of Norway spruce forests in Southern Germany

Long‐term effects of liming on microbial biomass and activity and soil organic matter (SOM) were investigated in samples from organic horizons (Of/Oh) in spruce forests at Adenau, Höglwald, Idar‐Oberstein, and Schluchsee (Southern Germany) where plots have been manually treated 7 to 13 years ago with dolomitic limestone. At all sites, pH values were markedly increased after liming. The contents of C and N in the organic horizons of the limed plots appeared to be lower with the greatest decrease at Höglwald (Dystric Luvisol) where liming has affected the soil properties for the longest time of all sites. Catalase activity was promoted after liming at Adenau (Cambic Podzol). This was also the case for the Dystric Luvisol where liming resulted also in higher basal respiration. Biomass‐C was higher in samples from the limed plot at Idar‐Oberstein (Dystric Cambisol). The ¹³C CPMAS NMR spectra of organic horizons from the control plots indicate no differences in the gross carbon composition of SOM. Furthermore, spectra from the limed Cambic Podzol, Dystric Cambisol, and Haplic Podzol (Schluchsee) were remarkably similar. However, for the Dystric Luvisol, the lime‐induced promotion of microbial activity resulted in lower O‐alkyl‐C intensity. The observed patterns of microbial biomass and activity were site‐dependent rather than a result of liming. Obviously liming had only small long‐term effects on the humus quality in the organic horizons, as far as detectable by CPMAS NMR spectroscopy. More sensitive techniques like pyrolysis‐GC/MS should be applied to analyze differences in C composition.     

What Characteristics of Soil Fertility Can Improve in Mixed Stands of Scots Pine and European Beech Compared with Monospecific Stands?

According to the current trends in forest management, endeavors are made to adjust the species composition to the site conditions and to increase the biodiversity. Changes in the species composition of forest stands lead to modifications of soil properties and nutrients cycle. The objective of the study was to evaluate the effect of monocultures (beech and pine) and mixed-species stands (pine-beech) on soil properties, particularly accumulation of soil organic carbon. We aim to demonstrate how different vegetation types influence soil properties in surface horizons of soil. The study sites are located in Germany and Poland under different tree stands Pinus sylvestris L., Fagus sylvatica L., and mixed-species stand. Contents of organic carbon and nitrogen, pH, and soil texture were analyzed. The studies conducted confirmed the positive effect of beech and mixed-species stands on acidification of surface soil horizons. We ordered the stands tested according to acidification effect on soils: pine stand > mixed stand > beech stand, which is consistent with previous studies. The most beneficial impact on the accumulation of organic carbon was observed in mixed-species stands in which beech and pine were found. Lower carbon-to-nitrogen (C/N) ratios confirm the high rate of organic matter decomposition and lower C/N ratio was reported in soil under beech stand in comparison to pine stands.     

Lignin and carbohydrates in soils under secondary forest,alley-cropping,and continuous farming,Thailand

This study was designed to investigate the impact of three land-use practices in Thailand on soil organic matter (SOM) composition. The land uses were continuous farming (till), alley-cropping, and secondary forest. Samples, taken from the top 10 cm soil surface, were fractionated into clay- (< 2 μm), silt- (2–20 μm), and sand-sized particles (20–2000 μm) prior to analyses of C, N, lignin-derived phenols and individual carbohydrates. As particle size increased, the C/N ratio and the concentration of lignin-derived phenols increased, whereas the degree of lignin oxidation as well as ratios of microbially derived hexoses to plant-derived pentoses decreased. Thus, the coarser the particle size, the less the SOM was altered by microbes. Seven years of alley-cropping increased SOM levels only little but considerably affected SOM composition by affecting the SOM of the sand fraction. The SOM concentration in the sand fraction increased in the order continuous farming < alley-cropping < secondary forest. In the same order, microbial alteration of lignin and carbohydrates of sand-sized SOM decreased. Both the different concentrations of SOM in the sand fractions as well as its different composition contributed, therefore, to different SOM among the sites. Increasing lignin-to-carbohydrate ratios for bulk soils and fractions in the order continuous farming < alley-cropping < secondary forest reflected such changes in SOM composition sensitively.     

Analyzing organic matter composition at intact biopore and crack surfaces by combining DRIFT spectroscopy and Pyrolysis‐Field Ionization Mass Spectrometry#

In the clay‐illuvial horizons (Bt) of Luvisols, surfaces of biopores and aggregates can be enriched in clay and organic matter (OM), relative to the bulk of the soil matrix. The OM composition of these coatings determines their bio‐physico‐chemical properties and is relevant for transport and transformation processes but is largely unknown at the molecular scale. The objective of this study was to improve the interpretation of spectra from Fourier transform infrared spectroscopy in diffuse reflectance mode (DRIFT) by using thermograms and released ion intensities obtained with pyrolysis‐field ionization mass spectrometry (Py‐FIMS) for a more detailed analysis of the mm‐scale spatial distribution of OM components at intact structural surfaces. Samples were separated from earthworm burrow walls, crack coatings, uncoated cracks, root channels, and pinhole fillings of the Bt‐horizons of Luvisols. The information from Py‐FI mass spectra enabled the assignment of OM functional groups also from spectral regions of overlapping DRIFT signal intensities to specific OM compound classes. In particular, bands from C=O and C=C bonds in the infrared range of wave numbers between 1,641 and 1,605 cm^?1 were related to heterocyclic N‐compounds, benzonitrile, and naphthalene. The OM at earthworm burrow walls was composed of chemically labile aliphatic C‐rich and rather stable lignin and alkylaromatic compounds whereas the OM of thick crack coatings and pinholes was dominated by heterocyclic N and nitriles and high‐molecular compounds, likely originating from combustion residues. In combination with Py‐FIMS, DRIFT applications to intact samples seem promising for generating a more detailed mm‐scale spatial distribution of OM‐related sorption and wettability properties of crack and biopore surfaces that may serve as preferential flow paths in structured soils.     

Soil organic matter composition and soil lightness

Relationships between soil lightness, soil organic matter (SOM) composition, content of organic C, CaCO₃, and texture were studied using 42 top‐soil horizons from different soil types located in southern Germany. SOM composition was determined by CPMAS ¹³C NMR spectroscopy, soil color was measured by diffuse‐reflectance spectrophotometry and given in the CIE L*a*b* color coordination system (Commission Internationale de l'Eclairage, 1978). Multiple‐regression analysis showed, that soil lightness of top‐soil horizons is principally determined by OC concentration, but CaCO₃ and soil texture are also major variables. Soil lightness decreased with increasing OC content. Carbonate content had an important effect on soil lightness even at low concentrations due to its lightening property. Regressions between soil lightness and organic C content were strongly linear, when the soils were differentiated according to texture and CaCO₃ content. The aryl‐C content was the only SOM component which correlated significantly with soil lightness (r_S = –0.87). In the linear regressions carried out on the different soil groups, soil aryl‐C content was a more significant predictor for soil lightness than total OC content.     

Long-term effects of mineral and organic fertilization on soil organic matter fractions and sorghum yield under Sudano-Sahelian conditions

Abstract. Knowledge of changes in soil organic matter (SOM) fractions resulting from agricultural practice is important for decision‐making at farm level because of the contrasting effects of different SOM fractions on soils. A long‐term trial sited under Sudano‐Sahelian conditions was used to assess the effect of organic and inorganic fertilization on SOM fractions and sorghum performance. Sorghum straw and kraal manure were applied annually at 10 t ha^?1, with and without urea at 60 kg N ha^?1. The other treatments included fallowing, a control (no fertilization), and inorganic fertilization only (urea, 60 kg N ha^?1). Fallowing gave significantly larger soil organic carbon and nitrogen (N) levels than any other treatment. Total soil SOM and N concentrations increased in the following order: urea only < straw < control < straw+urea < manure with or without urea < fallow. Farming had an adverse effect on SOM and N status; however, this mostly affected the fraction of SOM >0.053 mm (particulate organic matter, POM). The POM concentrations in the control, straw and urea‐only treatments were about one‐half of the POM concentrations in the fallow treatment. POM concentrations increased in the following order: urea only < control < straw with or without urea < manure with or without urea < fallow. The fraction of SOM <0.053 mm (fine organic matter, FOM) was greater than POM in all plots except in fallow and manure+urea plots. Total N concentration followed the same trend as SOM, but cultivation led to a decline in both POM‐N and FOM‐N. Crop yield was greatest in the manure plots and lowest in the straw, control and urea‐only plots. Results indicate that under Sudano‐Sahelian conditions, SOM, POM and FOM fractions and crop performance were better maintained using organic materials with a low C/N ratio (manure) than with organic material with a high C/N ratio (straw). Urea improved the effect of straw on crop yield and SOM concentration.