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.     

Cations adsorbed to soil organic matter — A regulatory factor for the release of organic carbon and hydrogen ions from soils to waters

Surface waters in northern forest ecosystems receive a substantial amount of drainage water from superficial soil horizons enriched in organic matter (SOM). Chemical reactions in the interface between the soil solution andf organic colloides will therefore affect the surface water chemistry. The mobilization of total organic carbon (TOC) and pH was studied as a function of amounts of organically adsorbed Na, Ca and Al in two O and one A horizon, which differed in the likelihood of contributing to the chemistry in runoff, in a forested watershed in northern Sweden. The samples were hydrogen ion saturated, washed and titrated with NaOH, Ca(OH)₂ and Al(OH)₃ in a constant ionic medium of 0.01 M NaCl in order to give rise to a population of manipulated samples differing in the composition of adsorbed cations. The highly humified SOM accumulated in the O_h and A_h horizons of a Gleysol close to the draining stream was stabilized by flocculating Al (95% of adsorbed metal cations), which resulted in a low release of TOC. These horizons showed a high potential of organic carbon solubility when Al was changed for di- or monovalent cations. Calculations suggested that the release of TOC would increase more than ten times if Al was exchanged for Ca upon liming to pH 6.0. The pH values of all horizons were shown to be determined mainly by the composition of adsorbed mono-,di- and trivalent cations.     

Analysis and simulation of soil organic‐carbon stocks in grassland ecosystems in SW Germany

Grassland extensification is followed by a change of soil organic‐matter (SOM) contents. In order to give a better assessment of these developments on grassland sites in SW Germany, the CENTURY Soil Organic Matter Model was used on five long‐term experimental sites under three different management practices (“Mowing”, “Mulching” (mowing without removal of the phytomass), and “Natural succession”). On these sites, soil‐organic‐carbon (SOC) monitoring was continuously done for soil depths of 0–4 and 4–8 cm from 1975 to 2002. The contents of organic carbon (OC) were at steady state or showed a slight decrease for the mulched and succession plots. Carbon contents of the mowed plots were decreasing. Measured C contents were transferred into stocks and compared with the simulated OC stocks. Linear regressions between observed and simulated C stocks were calculated separately for mulched and succession plots. The regressions for OC yielded significant relationships (R² = 0.8) for both kinds of plots. However, the model did not reproduce the short‐term dynamics of C stocks. Whereas SOC stocks on mulched and succession plots are expected to stay stable for the next decades according to the simulation, they are expected to decrease for a couple of years before stabilization on mowed plots.     

Impact of organic‐manure combinations on the productivity and soil quality in different cropping systems in central India

In a field experiment, the effect of combination of different organic manures on the productivity of crops and soil quality were evaluated in deep vertisols of central India. Combinations of cattle dung manure (CDM), poultry manure (PM), and vermicompost (VC) vis‐à‐vis mineral fertilizers were tested in four cropping systems involving soybean (Glycine max L.), durum wheat (Triticum durum Desf.), mustard (Brassica juncea L.), chickpea (Cicer arietinum L.), and isabgol (Plantago ovata Forsk). The organic manures were applied based on the N‐equivalent basis and nutrient requirement of individual crop. The grain yields of durum wheat and isabgol were higher in the treatment that received a combination of CDM + VC + PM whereas in mustard, CDM + PM and in chickpea, CDM + VC recorded the higher yields. The yield levels in these organic‐manure combinations were similar to the yields obtained with mineral fertilizers. Among the cropping systems, soybean–durum wheat and among the nutrient sources, the combination of CDM + VC + PM recorded the highest total productivity. At the end of the 3‐year cropping cycle, application of organic manures improved the soil‐quality parameters viz., soil organic carbon (SOC), soil available nutrients (N, P, and K), soil enzymes (dehydrogenase and alkaline phosphatase), and microbial biomass C in the top 0–15 cm soil. Bulk density and mean weight diameter of the soil were not affected by the treatments. Among the cropping systems, soybean–durum wheat recorded the highest SOC and accumulated higher soil available N, P, and K. In conclusion, the study clearly demonstrated that the manures applied in different combinations improved the soil quality and produced the grain yields which are at par with mineral fertilizers.     

Humification indices of water‐soluble fulvic acids derived from synchronous fluorescence spectra — effects of spectrometer type and concentration

The high variability of dissolved organic matter (DOM) in natural systems (concentration, composition) means rapid methods are required for its characterization so that a high number of samples can be analyzed. The objective of the present study was to quantify the effects of spectrometer type and dissolved organic carbon (DOC) concentration on the humification indices of water‐soluble fulvic acids (FAs) derived from synchronous fluorescence spectra, and thus enable the broader application of this method for DOM characterization. We used three standard FAs from the International Humic Substances Society, 24 water‐soluble FAs isolated from topsoil, groundwater and surface water in a fen area, and two different spectrometers. The wavelengths at which bands occurred were similar for all the FAs. Therefore, the differences between the spectra of the FAs studied could be described by humification indices (band ratios). The humification indices calculated correlated very well between spectrometers despite small differences in the wavelengths of bands and shoulders. The absolute values of these indices deduced from two spectrometers can only be directly compared if the spectra are corrected using a standard substance. Increasing DOC concentration resulted in a linear increase in humification indices with a sample specific slope. Therefore, we recommend using an uniformly low DOC concentration of about 10 mg C l^—1 for recording the spectra of samples with typically low DOC concentrations (aquatic samples, soil solutions). This value is a compromise between relatively low absorption to minimize inner filter effects and a sufficient signal‐to‐noise ratio.     

Conversion of cropland into grassland: Implications for soil organic‐carbon stocks in two soils with different texture

Soil organic‐carbon (SOC) stocks are expected to increase after conversion of cropland into grassland. Two adjacent cropland and grassland sites—one with a Vertisol with 23 y after conversion and one with an Arenosol 29 y after conversion—were sampled down to 60 cm depth. Concentrations of SOC and total nitrogen (N_tot) were measured before and after density fractionation in two light fractions and a mineral‐associated fraction with C adsorbed on mineral surfaces. For the soil profiles, SOC stocks and radiocarbon (¹⁴C) concentrations of mineral associated C were determined. Carbon stocks and mineral‐associated SOC concentrations were increased in the upper 10 cm of the grassland soil compared to the cropland. This corresponded to the root‐biomass distribution, with 59% and 86% of the total root biomass at 0–5 cm soil depth of the grasslands. However, at the Arenosol site, at 10–20 cm depth, C in the mineral‐associated fraction was lost 29 y after the conversion into grassland. Over all, SOC stocks were not significantly different between grassland and cropland at both sites when the whole profile was taken into account. At the Arenosol site, the impact of land‐use conversion on SOC accumulation was limited by low total clay surface area available for C stabilization. Subsoil C (30–50 cm) at cropland of the Vertisol site comprised 32% of the total SOC stocks with high ¹⁴C concentrations below the plowing horizon. We concluded that fresh C was effectively translocated into the subsoil. Thus, subsoil C has to be taken into account when land‐use change effects on SOC are assessed.     

Long‐term effects of fertilization on some soil properties under rainfed soybean‐wheat cropping in the Indian Himalayas

This study aims to examine the effects of long‐term fertilization and cropping on some chemical and microbiological properties of the soil in a 32 y old long‐term fertility experiment at Almora (Himalayan region, India) under rainfed soybean‐wheat rotation. Continuous annual application of recommended doses of chemical fertilizer and 10 Mg ha^–1 FYM on fresh‐weight basis (NPK + FYM) to soybean (Glycine max L.) sustained not only higher productivity of soybean and residual wheat (Triticum aestivum L.) crop, but also resulted in build‐up of total soil organic C (SOC), total soil N, P, and K. Concentration of SOC increased by 40% and 70% in the NPK + FYM–treated plots as compared to NPK (43.1 Mg C ha^–1) and unfertilized control plots (35.5 Mg C ha^–1), respectively. Average annual contribution of C input from soybean was 29% and that from wheat was 24% of the harvestable aboveground biomass yield. Annual gross C input and annual rate of total SOC enrichment from initial soil in the 0–15 cm layer were 4362 and 333 kg C ha^–1, respectively, for the plots under NPK + FYM. It was observed that the soils under the unfertilized control, NK and N + FYM treatments, suffered a net annual loss of 5.1, 5.2, and 15.8 kg P ha^–1, respectively, whereas the soils under NP, NPK, and NPK + FYM had net annual gains of 25.3, 18.8, and 16.4 kg P ha^–1, respectively. There was net negative K balance in all the treatments ranging from 6.9 kg ha^–1 y^–1 in NK to 82.4 kg ha^–1 y^–1 in N + FYM–treated plots. The application of NPK + FYM also recorded the highest levels of soil microbial‐biomass C, soil microbial‐biomass N, populations of viable and culturable soil microbes.     

Influence of fertilization and organic amendments on organic‐carbon fractions in Heilu soil on the loess plateau of China

The influence of fertilization on organic‐carbon fractions separated by density and particle size in Heilu soil (Calcic Kastanozems, FAO) was investigated in a 20‐year (1979–1999) long‐term experiment on the Loess Plateau of China. Compared to an unfertilized treatment, N application alone did not increase total organic carbon (TOC) and its fractions of density and particle size. However, the treatment of N + P fertilization significantly increased salty‐solution–soluble organic carbon (SSOC), microbial biomass C (MB‐C), and organic C associated with fine silt. When manure was applied alone and in combination with N and P fertilizer, the light fraction of organic C (LFOC), SSOC, and MB‐C were increased significantly, and the TOC was as high as that of a native Heilu soil. Organic C associated with different particle‐size fractions was also increased significantly, and the allocation of C among the fractions was altered: the proportions of C in sand (>50 μm), coarse‐silt (20–50 μm), and fine‐clay (<0.2 μm) fractions were increased whereas fine‐silt (2–20 μm) and coarse‐clay (0.2–2 μm) fractions were decreased. It is concluded that N fertilizer alone is not capable of restoring organic‐matter content in the Heilu soils of the Loess Plateau and that C‐containing material like manure and straw is necessary to produce significant increase in soil organic carbon in these soils.     

Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions

In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L^–1 and S_D values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L^–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.     

The application of biochar on soil acidity and other physico‐chemical properties of soils in southern Ethiopia

The aim of this research was to investigate the effect of biochar amendment on soil acidity and other physico‐chemical properties of soil in Southern Ethiopia using a field experiment of three treatments: (1) biochar made of corn cobs, (2) biochar made of chopped Lantana camara stem, and (3) biochar made of Eucalyptus globulus feedstock and a control, in which neither of the biochar was used. Each treatment had three levels of 6, 12 and 18 t ha⁻¹. The experiment was setup with RCBD in a factorial arrangement with three replications. In this regard, a total of 36 plots (each 2 × 2 m size) were applied with three replications to the depth of 0–15cm. From these 36 plots, composite soil samples were collected to the depth of 0–30 cm and analyzed for bulk density, total porosity, pH, soil organic carbon, total nitrogen, available phosphorus, potassium, and exchangeable acidity using standard procedures before and after biochar application. Two‐way ANOVA was also used to analyze the impact of the biochars on soil acidity and other properties. For the treatments that had significant effects, a mean separation was made using Least Significance Difference (LSD) test. The results showed the application of biochar significantly reduced, soil bulk density and exchangeable acidity when compared with a control (p < 0.05). Moreover, the total soil porosity, soil pH, total nitrogen, soil organic carbon, available phosphorus, and potassium were significantly increased in the soil. From among applied biochar treatments, Lantana camara applied at the level of 18 t ha⁻¹ had a higher impact in changing soil physico‐chemical properties. In general, the study suggests that the soil acidity can be reduced by applying biochar as it can amend other soil physico‐chemical properties.     

Carbon status and structural stability of soils from differing land use systems in the Kingdom of Tonga

Maintenance of soil carbon stocks is vital for the environment at large and for maintenance of soil chemical, physical and biological fertility. Tonga represents a country in agricultural transition from subsistence to commercial production and whilst this is good for the national economy the impact on soil resources is less clear. The major cropped soils, fallow vegetation types and forest systems of Tonga were identified in each island group and samples of representative soils (0.15 m depth) from each land use unit were taken. Total carbon (C_T) and δ¹³C were measured and labile carbon (C_L) determined by oxidation with 333 mm KMnO₄. These data were used to determine the carbon management index (CMI) and the proportion of carbon from C4 species in the C_T pool. Relative to primary forest, the soil C_T and C_L generally declined with changes in vegetation and more intense mechanical tillage. The contribution of C4 plants to soil C increased with intensity of mechanical tillage and the prevalence of C4 guinea grass (Panicum maximum Jacquin) fallow. The changes in soil C were reflected in the CMI, and C_L was a more sensitive indicator of change than C_T. These data indicates that all land use systems have experienced a large net loss of soil C relative to the forest systems. Soil mean weight diameter (MWD) decreased significantly with increased intensity of mechanical tillage and to a lesser extent with the intensity and length of cropping. The relationship between soil MWD and soil C was similar with soil C_T and C_L. Grass fallow was as effective as permanent vegetation systems in improving soil MWD and lowering the micro‐aggregate (<125 μm) fraction.     

Addition of lignin to lime materials for expedited pH increase and improved vertical mobility of lime in no‐till soils

Soil acidification caused by long‐term nitrogen (N) fertilizer applications has been a growing concern for dryland crop production in both tilled and no‐till soils in the Pacific Northwest (PNW). Many no‐till soils have stratified soil pH in the 5–10 cm depth due to repeated N fertilizer applications at this depth. In the PNW, the practice of liming to correct low soil pH is complicated due to lack of affordable lime sources and because the inherent difficulty in ameliorating stratified soil acidity in no‐till systems. An intact soil‐column incubation study was conducted to investigate whether mixing lime materials with lignin‐containing black liquor—a by‐product from the pulp industry—could elevate soil pH change in both conventional and no‐till systems and expedite vertical downward movement of lime in no‐till system. Results indicate that mixing lime with black liquor has the potential to not only elevate the increase in soil pH in both conventional till and no‐till systems, but also accelerate downward movement of lime to correct soil pH below the soil surface. Mixing agricultural lime or super fine micro lime with black liquor increased soil pH to a depth of 25–30 cm within 147 days after surface application to a no‐till soil.     

Effects of compost on the chemical composition of SOM in density and aggregate fractions from rice–wheat cropping systems as shown by solid‐state 13C‐NMR spectroscopy

The 4‐year application of pig‐manure compost (PMC) to crop fields in Jiangsu significantly increased organic‐C and total N concentrations compared to chemical fertilization and control treatment. To identify the soil processes that led to these changes, ¹³C cross‐polarization magic‐angle spinning nuclear‐magnetic resonance (¹³C CPMAS NMR) and dipolar‐dephasing nuclear‐magnetic‐resonance spectroscopy (DD NMR) were conducted on soil organic matter (SOM) fractions separated by wet‐sieving and density fractionation procedures. This allowed characterization of the SOM quality under three contrasting fertilizer regimes. The results indicate that PMC application can alter the distribution of functional groups and improve alkyl C‐to‐O‐alkyl C ratios compared to chemical‐fertilizer treatment (CF). Alkyl C contents were increased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) for all treatments, suggesting that recalcitrant material accumulates in the microaggregate fractions. The O‐alkyl C contents were decreased from macroaggregate fractions (> 2 mm) to microaggregate fractions (0.05–0.25 mm) under CF and PMC treatments, while no consistent trend was found for the control (NF) treatment. The alkyl C‐to‐O‐alkyl C ratios in macroaggregates were lower than those in microaggregates, indicating that the degrees of SOM decomposition were lower in macroaggregates compared to microaggregates. In all aggregate‐size classes, the amount of organic matter appeared to depend on the fertilization regime. This study provides useful information regarding the buildup of organic material in soil from long‐term manure‐compost enrichment.     

Use of mid‐infrared spectroscopy in the diffuse‐reflectance mode for the prediction of the composition of organic matter in soil and litter

Mid‐infrared spectroscopy (MIRS) is assumed to be superior to near‐infrared spectroscopy (NIRS) for the prediction of soil constituents, but its usefulness is still not sufficiently explored. The objective of this study was to evaluate the ability of MIRS to predict the chemical and biological properties of organic matter in soils and litter. Reflectance spectra of the mid‐infrared region including part of the near‐infrared region (7000–400 cm^–1) were recorded for 56 soil and litter samples from agricultural and forest sites. Spectra were used to predict general and biological characteristics of the samples as well as the C composition which was measured by ¹³C CPMAS‐NMR spectroscopy. A partial least‐square method and cross‐validation were used to develop equations for the different constituents over selected spectra ranges after several mathematical treatments of the spectra. Mid‐infrared spectroscopy predicted well the C : N ratio: the modeling efficiency EF was 0.95, the regression coefficient (a) of a linear regression (measured against predicted values) was 1.0, and the correlation coefficient (r) was 0.98. Satisfactorily (EF ≥ 0.70, 0.8 ≤ a ≤ 1.2, r ≥ 0.80) assessed were the contents of C, N, and lignin, the production of dissolved organic carbon, and the contents of carbonyl C, aromatic C, O‐alkyl C, and alkyl C. However, the N mineralization rate, the microbial biomass and the alkyl–to–aromatic C ratio were predicted less satisfactorily (EF < 0.70). Limiting the sample set to mineral soils did generally not result in improved predictions. The good and satisfactory predictions reported above indicate a marked usefulness of MIRS in the assessment of chemical characteristics of soils and litter, but the accuracies of the MIRS predictions in the diffuse‐reflectance mode were generally not superior to those of NIRS.     

Acidity,nutrient stocks,and organic‐matter content in soils of a temperate deciduous forest with different abundance of European beech (Fagus sylvatica L.)

The production and composition of leaf litter, soil acidity, exchangeable nutrients, and the amount and distribution of soil organic matter were analyzed in a broad‐leaved mixed forest on loess over limestone in Central Germany. The study aimed at determining the current variability of surface‐soil acidification and nutrient status, and at identifying and evaluating the main factors that contributed to the variability of these soil properties along a gradient of decreasing predominance of European beech (Fagus sylvatica L.) and increasing tree‐species diversity. Analyses were carried out in (1) mature monospecific stands with a predominance of beech (DL 1), (2) mature stands dominated by three deciduous‐tree species (DL 2: beech, ash [Fraxinus excelsior L.], lime [Tilia cordata Mill. and/or T. platyphyllos Scop.]), and (3) mature stands dominated by five deciduous‐tree species (DL 3: beech, ash, lime, hornbeam [Carpinus betulus L.], maple [Acer pseudoplatanus L. and/or A. platanoides L.]). The production of leaf litter was similar in all stands (3.2 to 3.9 Mg dry matter ha^–1 y^–1) but the total quantity of Ca and Mg deposited on the soil surface by leaf litter increased with increasing tree‐species diversity and decreasing abundance of beech (47 to 88 kg Ca ha^–1 y^–1; 3.8 to 7.9 kg Mg ha^–1 y^–1). The soil pH_(H2O) and base saturation (BS) measured at three soil depths down to 30 cm (0–10 cm, 10–20 cm, 20–30 cm) were lower in stands dominated by beech (pH = 4.2 to 4.4, BS = 15% to 20%) than in mixed stands (pH = 5.1 to 6.5, BS = 80% to 100%). The quantities of exchangeable Al and Mn increased with decreasing pH and were highest beneath beech. Total stocks of exchangeable Ca (0–30 cm) were 12 to 15 times larger in mixed stands (6660 to 9650 kg ha^–1) than in beech stands (620 kg ha^–1). Similar results were found for stocks of exchangeable Mg that were 4 to 13 times larger in mixed stands (270 to 864 kg ha^–1) than in beech stands (66 kg ha^–1). Subsoil clay content and differences in litter composition were identified as important factors that contributed to the observed variability of soil acidification and stocks of exchangeable Ca and Mg. Organic‐C accumulation in the humus layer was highest in beech stands (0.81 kg m^–2) and lowest in stands with the highest level of tree‐species diversity and the lowest abundance of beech (0.27 kg m^–2). The results suggest that redistribution of nutrients via leaf litter has a high potential to increase BS in these loess‐derived surface soils that are underlain by limestone. Species‐related differences of the intensity of soil–tree cation cycling can thus influence the rate of soil acidification and the stocks and distribution of nutrients.     

Comparing the thermal conductivity of three artificial soils under differing moisture and density conditions for use in green infrastructure

Soil-based green infrastructure has the potential to improve building thermal performance and contribute to sustainable buildings. This study compares thermal conductivity response to soil moisture of three peat-free artificial soils to evaluate their potential use within green roofs and living walls. Thermal conductivity was measured with changing soil moisture and density. All soils showed higher thermal conductivity measures with increases in soil moisture. The ‘Biochar-coconut coir compost’ had the lowest thermal conductivity measures which displayed negligible response to density changes and exhibited the highest water holding capacity. When uncompacted, ‘FabSoil’ had low thermal conductivity measures, but when compacted, its measures were considerably higher. Results show the role of density on thermal performance will be soil type dependent. Overall, findings highlight the importance of considering substrate composition, density and suggest that peat-free artificial soil substrates that contain biochar, have a higher percentage organic matter content and a finer particle texture are likely to result in lower thermal conductivity and higher soil water holding capacity. The results also showed that ThetaProbe measures (volumetric) had a high equivalence to actual soil moisture content (gravimetric), across different soil types and soil bulk densities. This finding supports the use of ThetaProbe measures as an effective method for monitoring soil moisture; with the potential for integration into irrigation control systems for green infrastructure. The findings of this paper offer the potential to improve building thermal performance by informing soil substrate choice, irrigation control and load bearing requirements in the design of green infrastructure.     

Kinetics of the release of dissolved organic matter (DOM) from air‐dried and pre‐moistened soil material

In this study, the kinetics of soil organic matter (SOM) dissolution from soil samples in different states of moisture was investigated, using a continuous extraction method. The investigation distinguished three processes of SOM dissolution. They include an initial, fast process (probably hydrophilic dissolved organic matter) and two slow, rate limited processes, which probably correspond to hydrophobic dissolved organic matter (DOM). The second process indicates a slow, continuous release of DOM, whereas the third process is determined by a power law. The rate of the third process strongly depends on temperature and state of moisture. It is diffusion limited, with the diffusion control probably being located in the solid soil organic matter. This was explained by a gel structure, which slowly forms in the hydrating SOM and allows diffusion of mobile particles of SOM. The results show the importance of considering the moisture state of SOM for the kinetics of DOM dissolution.     

Quantification of long‐chain fatty acids in dissolved organic matter and soils

The objective was to develop and adapt a versatile analytical method for the quantification of solvent extractable, saturated long‐chain fatty acids in aquatic and terrestrial environments. Fulvic (FA) and humic (HA) acids, dissolved organic matter (DOM) in water, as well as organic matter in whole soils (SOM) of different horizons were investigated. The proposed methodology comprised extraction by dichloromethane/acetone and derivatization with tetramethylammonium hydroxide (TMAH) followed by gas chromatography/mass spectrometry (GC/MS) and library searches. The C_10:0 to C_34:0 methyl esters of n‐alkyl fatty acids were used as external standards for calibration. The total concentrations of C_14:0 to C_28:0 n‐alkyl fatty acids were determined in DOM obtained by reverse‐osmosis of Suwannee river water (309.3 μg g^—1), in freeze‐dried brown lake water (180.6 μg g^—1), its DOM concentrate (93.0 μg g^—1), humic acid (43.1 μg g^—1), and fulvic acid (42.5 μg g^—1). The concentrations of the methylated fatty acids (n‐C_16:0 to n‐C_28:0) were significantly (r² = 0.9999) correlated with the proportions of marker signals (% total ion intensity (TII), m/z 256 to m/z 508) in the corresponding pyrolysis‐field ionization (FI) mass spectra. The concentrations of terrestrial C_10:0 to C_34:0 n‐alkyl fatty acids from four soil samples ranged from 0.02 μg g^—1 to 11 μg g^—1. The total concentrations of the extractable fatty acids were quantified from a Podzol Bh horizon (26.2 μg g^—1), Phaeozem Ap unfertilized (48.1 μg g^—1), Phaeozem Ap fertilized (57.7 μg g^—1), and Gleysol Ap (66.7 μg g^—1). Our results demonstrate that the method is well suited to investigate the role of long‐chain fatty acids in humic fractions, whole soils and their particle‐size fractions and can be serve for the differentiation of plant growth and soil management.