Usefulness of near‐infrared spectroscopy for the prediction of chemical and biological soil properties in different long‐term experiments

The prediction accuracy of visible and near‐infrared (Vis‐NIR) spectroscopy for soil chemical and biological parameters has been variable and the reasons for this are not completely understood. Objectives were (1) to explore the predictability of a series of chemical and biological properties for three different soil populations and—based on these heterogeneous data sets—(2) to analyze possible predictive mechanisms statistically. A number of 422 samples from three arable soils in Germany (a sandy Haplic Cambisol and two silty Haplic Luvisols) of different long‐term experiments were sampled, their chemical and biological properties determined and their reflectance spectra in the Vis‐NIR region recorded after shock‐freezing followed by freeze‐drying. Cross‐validation was carried out for the entire population as well as for each population from the respective sites. For the entire population, excellent prediction accuracies were found for the contents of soil organic C (SOC) and total P. The contents of total N and microbial biomass C and pH were predicted with good accuracy. However, prediction accuracy for the other properties was less: content of total S was predicted approximately quantitatively, whereas Vis‐NIR spectroscopy could only differentiate between high and low values for the contents of microbial N, ergosterol, and the ratio of ergosterol to microbial biomass C. Contents of microbial biomass P and S, basal respiration, and qCO₂ could not be predicted. Prediction accuracies were greatest for the entire population and the Luvisol at Garte, followed by the Luvisol at Hohes Feld, whereas the accuracy for the sandy Cambisol was poor. The poor accuracy for the sandy Cambisol may have been due to only smaller correlations between the measured properties and the SOC content compared to the Luvisols or due to a general poor prediction performance for sandy soils. Another reason for the poor accuracy may have been the smaller range of contents in the sandy soil. Overall, the data indicated that the accuracy of predictions of soil properties depends largely on the population investigated. For the entire population, the usefulness of Vis‐NIR for the number of chemical and biological soil properties was evident by markedly greater correlation coefficients (measured against Vis‐NIR predicted) compared to the Pearson correlation coefficients of the measured properties against the SOC content. However, the cross‐validation results are valid only for the closed population used in this study.     

Simultaneous assessment of key properties of arid soil by combined PXRF and Vis–NIR data

Arid soil is common worldwide and has unique properties that often limit agronomic productivity, specifically, salinity expressed as soluble salts and large amounts of calcium carbonate and gypsum. Currently, the most common methods for evaluating these properties in soil are laboratory‐based techniques such as titration, gasometry and electrical conductivity. In this research, we used two proximal sensors (portable X‐ray fluorescence (PXRF) and visible near‐infrared diffuse reflectance spectroscopy (Vis–NIR DRS)) to scan a diverse set (n = 116) of samples from arid soil in Spain. Then, samples were processed by standard laboratory procedures and the two datasets were compared with advanced statistical techniques. The latter included penalized spline regression (PSR), support vector regression (SVR) and random forest (RF) analysis, which were applied to Vis–NIR DRS data, PXRF data and PXRF and Vis–NIR DRS data, respectively. Independent validation (30% of the data) of the calibration equations showed that PSR + RF predicted gypsum with a ratio of performance to interquartile distance (RPIQ) of 5.90 and residual prediction deviation (RPD) of 4.60, electrical conductivity (1:5 soil : water) with RPIQ of 3.14 and RPD of 2.10, Ca content with RPIQ of 2.92 and RPD of 2.07 and calcium carbonate equivalent with RPIQ of 2.13 and RPD of 1.74. The combined PXRF and Vis–NIR DRS approach was superior to those that use data from a single proximal sensor, enabling the prediction of several properties from two simple, rapid, non‐destructive scans.     

Comparison of Near Infrared Reflectance Spectroscopy with Combustion and Chemical Methods for Soil Carbon Measurements in Agricultural Soils

As interest in soil organic carbon (SOC) dynamics increases, so do needs for rapid, accurate, and inexpensive methods for quantifying SOC. Objectives were to i) evaluate near infrared reflectance (NIR) spectroscopy potential to determine SOC and soil organic matter (SOM) in soils from across Tennessee, USA; and ii) evaluate potential upper limits of SOC from forest, pasture, no-tillage, and conventional tilled sites. Samples were analyzed via dry-combustion (SOC), Walkley–Black chemical SOM, and NIR. In addition, the sample particle size was classified to give five surface roughness levels to determine effects of particle size on NIR. Partial least squares regression was used to develop a model for predicting SOC as measured by NIR by comparing against SOM and SOC. Both NIR and SOM correlated well (R² > 0.9) with SOC (combustion). NIR is therefore considered a sufficiently accurate method for quantifying SOC in soils of Tennessee, with pasture and forested systems having the greatest accumulations.Abbreviations SOC, soil organic carbon; NIR, Near Infrared Reflectance Spectroscopy; MTREC, Middle Tennessee Research and Education Center; RECM, Research and Education Center at Milan; PREC, Plateau Research and Education Center; PLS, Partial least squares.     

Calibration of visible and near infrared spectroscopy for soil analysis at the field scale on three European farms

The development of accurate calibration models for selected soil properties is a crucial prerequisite for successful implementation of visible and near infrared (Vis‐NIR) spectroscopy for soil analysis. This paper compares the performance of calibration models developed for individual farms with that of general models valid for three farms in three European countries. Fresh soil samples collected from farms in the Czech Republic, Germany and Denmark were scanned with a fibre‐type Vis‐NIR spectrophotometer. After dividing spectra into calibration (70%) and validation (30%) sets, spectra in the calibration set were subjected to partial least squares regression (PLSR) with leave‐one‐out cross‐validation to establish calibration models of soil properties. Except for the Czech Republic farm, individual farm models provided successful calibration for total carbon (TC), total nitrogen (TN) and organic carbon (OC), with coefficients of determination (R²) of 0.85–0.93 and 0.74–0.96 and residual prediction deviations (RPD) of 2.61–3.96 and 2.00–4.95 for the cross‐validation and independent validation respectively. General calibration models gave improved prediction accuracies compared with models of farms in the Czech Republic and Germany, which was attributed to larger ranges in the variation of soil properties in general models compared with those in individual farm models. The results revealed that larger standard deviations (SDs) and wider variation ranges have resulted in larger R² and RPD, but also larger root mean square errors of prediction (RMSEP). Therefore, a compromise solution, which also results in small RMSEP values, should be found when selecting soil samples for Vis‐NIR calibration to cover a wide variation range.     

Improved analysis and modelling of soil diffuse reflectance spectra using wavelets

Diffuse reflectance spectroscopy using visible (vis), near‐infrared (NIR) and mid‐infrared (mid‐IR) energy can be a powerful tool to assess and monitor soil quality and function. Mathematical pre‐processing techniques and multivariate calibrations are commonly used to develop spectroscopic models to predict soil properties. These models contain many predictor variables that are collinear and redundant by nature. Partial least squares regression (PLSR) is often used for their analysis. Wavelets can be used to smooth signals and to reduce large data sets to parsimonious representations for more efficient data storage, computation and transmission. Our aim was to investigate their potential for the analyses of soil diffuse reflectance spectra. Specifically we wished to: (i) show how wavelets can be used to represent the multi‐scale nature of soil diffuse reflectance spectra, (ii) produce parsimonious representations of the spectra using selected wavelet coefficients and (iii) improve the regression analysis for prediction of soil organic carbon (SOC) and clay content. We decomposed soil vis‐NIR and mid‐IR spectra using the discrete wavelet transform (DWT) using a Daubechies’s wavelet with two vanishing moments. A multiresolution analysis (MRA) revealed their multi‐scale nature. The MRA identified local features in the spectra that contain information on soil composition. We illustrated a technique for the selection of wavelet coefficients, which were used to produce parsimonious multivariate calibrations for SOC and clay content. Both vis‐NIR and mid‐IR data were reduced to less than 7% of their original size. The selected coefficients were also back‐transformed. Multivariate calibrations were performed by PLSR, multiple linear regression (MLR) and MLR with quadratic polynomials (MLR‐QP) using the spectra, all wavelet coefficients, the selected coefficients and their back transformations. Calibrations by MLR‐QP using the selected wavelet coefficients produced the best predictions of SOC and clay content. MLR‐QP accounted for any nonlinearity in the data. Transforming soil spectra into the wavelet domain and producing a smaller representation of the data improved the efficiency of the calibrations. The models were computed with reduced, parsimonious data sets using simpler regressions.     

Discriminating soil crust type,development stage and degree of disturbance in semiarid environments from their spectral characteristics

Biological soil crusts (BSCs) are increasingly recognized as common features in arid and semiarid ecosystems and play an important role in the hydrological and ecological functioning of these ecosystems. However, BSCs are very vulnerable to, in particular, human disturbance. This results in a complex spatial pattern of BSCs in various stages of development. Such patterns, to a large extent, determine runoff and erosion processes in arid and semiarid ecosystems. In recent years, visible and near infrared (Vis‐NIR) diffuse reflectance spectroscopy has been used for large‐scale mapping of the distribution of BSCs. Our goals were (i) to demonstrate the efficiency of Vis‐NIR spectroscopy in discriminating vegetation, physical soil crusts, various developmental stages of BSCs, and various types of disturbance on BSCs and (ii) to develop a classification system for these types of ground cover based on Vis‐NIR spectroscopy. Spectral measurements were taken of vegetation, physical crusts and various types of BSCs prior to, and following, trampling or removal with a scraper in two semiarid areas in SE Spain. The main spectral differences were: (i) absorption by water at about 1450 nm, more intense in the spectra of vegetation than in those of physical crusts or BSCs, (ii) absorption features at about 500 and 680 nm for the BSCs, which were absent or very weak for physical crusts, (iii) a shallower slope between about 750 and 980 nm for physical crusts and early‐successional BSCs than for later‐successional BSCs and (iv) a steeper slope between about 680 and 750 nm for the most developed BSCs. A partial least squares regression‐linear discriminant analysis of the spectral data resulted in a reliable classification (Kappa coefficients over 0.90) of the various types of ground cover and types of BSC disturbance. The distinctive spectral features of vegetation, physical crusts and the various developmental stages of BSCs were used to develop a classification system. This will be a promising tool for mapping BSCs with hyperspectral remote sensing.     

Prediction of volumetric soil organic carbon from field‐moist intact soil cores

This study investigated the potential for visible–near‐infrared (vis–NIR) spectroscopy to predict locally volumetric soil organic carbon (SOC) from spectra recorded from field‐moist soil cores. One hundred cores were collected from a 71‐ha arable field. The vis–NIR spectra were collected every centimetre along the side of the cores to a depth of 0.3 m. Cores were then divided into 0.1‐m increments for laboratory analysis. Reference SOC measurements were used to calibrate three partial least‐squares regression (PLSR) models for bulk density (ρ_b), gravimetric SOC (SOC_g) and volumetric SOC (SOC_v). Accurate predictions were obtained from averages of spectra from those 0.1‐m increments for SOC_g (ratio of performance to inter‐quartile (RPIQ) = 5.15; root mean square error (RMSE) = 0.38%) and SOC_v (RPIQ = 5.25; RMSE = 4.33 kg m^?3). The PLSR model for ρ_b performed least well, but still produced accurate results (RPIQ = 3.76; RMSE = 0.11 Mg m^?3). Predictions for ρ_b and SOC_g were combined to compare indirect and direct predictions of SOC_v. No statistical difference in accuracy between these approaches was detected, suggesting that the direct prediction of SOC_v is possible. The PLSR models calibrated on the 10‐cm depth intervals were also applied to the spectra originally recorded on a 1‐cm depth increment. While a bigger bias was observed for 1‐cm than for 10‐cm predictions (1.13 and 0.19 kg m^?3, respectively), the two populations of estimates were not distinguishable statistically. The study showed the potential for using vis–NIR spectroscopy on field‐moist soil cores to predict SOC at high depth resolutions (1 cm) with locally derived calibrations.     

Modelling soil organic carbon concentration of mineral soils in arable land using legacy soil data

Soil organic carbon (SOC) concentration is an essential factor in biomass production and soil functioning. SOC concentration values are often obtained by prediction but the prediction accuracy depends much on the method used. Currently, there is a lack of evidence in the soil science literature as to the advantages and shortcomings of the different commonly used prediction methods. Therefore, we compared and evaluated the merits of the median approach, analysis of covariance, mixed models and random forests in the context of prediction of SOC concentrations of mineral soils under arable management in the A‐horizon. Three soil properties were used in all of the developed models: soil type, physical clay content (particle size <0.01 mm) and A‐horizon thickness. We found that the mixed model predicted SOC concentrations with the smallest mean squared error (0.05%²), suggesting that a mixed‐model approach is appropriate if the study design has a hierarchical structure as in our scenario. We used the Estonian National Soil Monitoring data on arable lands to predict SOC concentrations of mineral soils. Subsequently, the model with the best prediction accuracy was applied to the Estonian digital soil map for the case study area of Tartu County where the SOC predictions ranged from 0.6 to 4.8%. Our study indicates that predictions using legacy soil maps can be used in national inventories and for up‐scaling estimates of carbon concentrations from county to country scales.     

Can Near or Mid‐Infrared Diffuse Reflectance Spectroscopy Be Used to Determine Soil Carbon Pools?

Abstract

The objective of this study was to compare mid‐infrared (MIR) an near‐infrared (NIR) spectroscopy (MIRS and NIRS, respectively) not only to measure soil carbon content, but also to measure key soil organic C (SOC) fractions and the δ¹³C in a highly diverse set of soils while also assessing the feasibility of establishing regional diffuse reflectance calibrations for these fractions. Two hundred and thirty‐seven soil samples were collected from 14 sites in 10 western states (CO, IA, MN, MO, MT, ND, NE, NM, OK, TX). Two subsets of these were examined for a variety of C measures by conventional assays and NIRS and MIRS. Biomass C and N, soil inorganic C (SIC), SOC, total C, identifiable plant material (IPM) (20× magnifying glass), the ratio of SOC to the silt+clay content, and total N were available for 185 samples. Mineral‐associated C fraction, δ¹³C of the mineral associated C, δ¹³C of SOC, percentage C in the mineral‐associated C fraction, particulate organic matter, and percentage C in the particulate organic matter were available for 114 samples. NIR spectra (64 co‐added scans) from 400 to 2498 nm (10‐nm resolution with data collected every 2 nm) were obtained using a rotating sample cup and an NIRSystems model 6500 scanning monochromator. MIR diffuse reflectance spectra from 4000 to 400 cm^?1 (2500 to 25,000 nm) were obtained on non‐KBr diluted samples using a custom‐made sample transport and a Digilab FTS‐60 Fourier transform spectrometer (4‐cm^?1 resolution with 64 co‐added scans). Partial least squares regression was used with a one‐out cross validation to develop calibrations for the various analytes using NIR and MIR spectra. Results demonstrated that accurate calibrations for a wide variety of soil C measures, including measures of δ¹³C, are feasible using MIR spectra. Similar efforts using NIR spectra indicated that although NIR spectrometers may be capable of scanning larger amounts of samples, the results are generally not as good as achieved using MIR spectra.     

Sample preparation and selection for qualitative and quantitative analyses of soil organic carbon with mid‐infrared reflectance spectroscopy

Mid‐infrared spectroscopy (MIRS) is a well‐established analytical tool for qualitative and quantitative analysis of soil samples. However, effects of soil sample grinding procedures on the prediction accuracy of MIR models and on qualitative spectral information have not been well investigated and, in consequence, not standardized up to now. Further, the effects of soil sample selection on the accuracy of MIR prediction models has not been quantified yet. This study investigated these effects by using 180 well‐characterized soil samples that were ground for different times (0, 2 or 4 minutes) and then used for MIR measurements. To study the impact of sample preparation, soil spectra were subjected to principal component analyses (PCA), multiple regression and partial least square (PLS) analysis. The results indicate that the prediction accuracy of MIR models for soil organic carbon (SOC) and pH and the qualitative spectral information were better overall for lightly ground (2 minutes) soil samples compared with intensively (4 minutes) or unground soil samples. Whereas the grinding procedure did not show any effect on spectra of clay minerals, spectral information for quartz and for SOC was modified. Even though it is difficult to recommend a global standardized soil sample grinding procedure for MIR measurements because of different mill types available within laboratories, we highly recommend using an internally standardized grinding procedure. Moreover, we show that neither land use nor soil sampling depth influences the prediction of the SOC content. However, sand and clay content substantially affect the score vectors used by the PLS algorithm to predict the SOC content. Thus, we recommend using soil samples similar in texture for more precise SOC calibration models for MIR spectroscopy.     

Influence of basin‐based conservation agriculture on selected soil quality parameters under smallholder farming in Zimbabwe

The research was carried out to determine the effect of basin‐based conservation agriculture (CA) on selected soil quality parameters. Paired plots (0.01 ha) of CA and conventional tillage based on the animal‐drawn mouldboard plough (CONV) were established between 2004 and 2007 on farm fields on soils with either low (12–18% – sandy loams and sandy clay loams) or high clay levels (>18–46% – sandy clays and clays) as part of an ongoing project promoting CA in six districts in the smallholder farming areas of Zimbabwe. We hypothesized that CA would improve soil organic carbon (SOC), bulk density, aggregate stability, soil moisture retention and infiltration rate. Soil samples for SOC and aggregate stability were taken from 0 to 15 cm depth and for bulk density and soil moisture retention from 0 to 5, 5 to 10 and 10 to 15 cm depths in 2011 from maize plots. Larger SOC contents, SOC stocks and improved aggregate stability, decreased bulk density, increased pore volume and moisture retention were observed in CA treatments. Results were consistent with the hypothesis, and we conclude that CA improves soil quality under smallholder farming. Benefits were, however, greater in high clay soils, which is relevant to the targeting of practices on smallholder farming areas of sub‐Saharan Africa.     

Influence of the number of samples on prediction error of visible and near infrared spectroscopy of selected soil properties at the farm scale

This paper reports on the influence of the number of samples used for the development of farm‐scale calibration models for moisture content (MC), total nitrogen (TN) and organic carbon (OC) on the prediction error expressed as root mean square error of prediction (RMSEP) for visible and near infrared (vis‐NIR) spectroscopy. Fresh (wet) soil samples collected from four farms in the Czech Republic, Germany, Denmark and the UK were scanned with a fibre‐type vis‐NIR, AgroSpec spectrophotometer with a spectral range of 305–2200 nm. Spectra were divided into calibration (two thirds) and prediction (one third) sets and the calibration spectra were subjected to a partial least squares regression (PLSR) with leave‐one‐out cross‐validation using Unscrambler 7.8 software. The RMSEP values of models with a large sample number (46–84 samples from each farm) were compared with those of models developed with a small sample number (25 samples selected from the large sample set of each farm) for the same variation range. Both large‐set and small‐set models were validated by the same prediction set for each property. Further PLSR analysis was carried out on samples from the German farm, with different sample numbers of the calibration set of 25, 50, 75 and 100 samples. Results showed that the large‐size dataset models resulted in smaller RMSEP values than the small‐size dataset models for all the soil properties studied. The results also demonstrated that with the increase in sample number used in the calibration set, RMSEP decreased in almost linear fashion, although the largest decrease was between 25 and 50 samples. Therefore, it is recommended that the number of samples should be chosen according to the accuracy required, although 50 soil samples is considered appropriate in this study to establish calibration models of TN, OC and MC with smaller expected prediction errors as compared with smaller sample numbers.     

How do hedgerows influence soil organic carbon stock in livestock‐grazed pasture?

Hedgerows have the potential to influence ecosystem function in livestock‐grazed pasture. Despite this, they are often ignored when quantifying farmland ecosystem service delivery. In this study, we assess the contribution of hedgerows to the ecosystem function of carbon (C) storage, with a particular emphasis on soil organic carbon (SOC). We measured SOC stock (kg C m^?2), on an equivalent soil mass basis, at 0–0.15 m depth in pasture adjacent to 38 hedgerows (biotic) and 16 stone walls or fences (abiotic controls) across ten farms in the county of Conwy, Wales, UK. Pasture SOC stock (~7 kg C m^?2) was similar adjacent to biotic and abiotic field boundaries, positively associated with soil moisture and negatively with soil bulk density (BD). For biotic boundaries, two further variables were significantly associated with SOC stock, distance from hedgerow (decrease in SOC stock) and slope orientation (upslope SOC stock greater than downslope). For pasture adjacent to hedgerows, a model combining the aforementioned variables (BD, soil moisture, distance from hedgerow, slope orientation) explained 78% of variation in SOC stock. This study demonstrates that whilst hedgerows do have subtle positive effects on SOC stock in adjacent pasture, SOC storage adjacent to field boundaries is influenced more by soil moisture content and BD than field boundary type.     

Development of a Near‐Infrared Imaging System for Determination of Rice Moisture

The objective of this study was to develop a near‐infrared (NIR) imaging system to determine rice moisture content. The NIR imaging system fitted with 15 band‐pass filters (wavelengths of 870–1,014 nm) was used to capture the spectral image. In this work, calibration methods including multiple linear regression (MLR), partial least squares regression (PLSR), and artificial neural network (ANN) were used in both near‐infrared spectrometry (NIRS) and the NIR imaging system to determine the moisture content of rice. Comprehensive performance comparison among MLR, PLSR, and ANN approaches has been conducted. To reduce repetition and redundancy in the input data and obtain a more accurate network, six significant wavelengths selected by the MLR model, which had high correlation with the moisture content of rice, were used as the input data of the ANN. The performance of the developed system was evaluated through experimental tests for rice moisture content. This study adopted the coefficient of determination (r_val²), the standard error of prediction (SEP), and the relative performance determinant (RPD) as the performance indices of the NIR imaging system with respect to the tests of rice moisture content. Utilizing these three models, the analysis results of r_val², SEP, and RPD for the validation set were within 0.942–0.952, 0.435–0.479%, and 4.2–4.6, respectively. From experimental results, the performance of NIR imaging system was almost the same as that of NIRS. Using the developed NIR imaging system, all of the three different calibration methods (MLR, PLSR, and ANN) provided a high prediction capacity for the determination of moisture in rice samples. These results indicated that the NIR imaging system developed in this study can be used as a device for the measurement of rice moisture content.     

Prediction of soil organic matter using a spatially constrained local partial least squares regression and the Chinese vis–NIR spectral library

We need to determine the best use of soil vis–NIR spectral libraries that are being developed at regional, national and global scales to predict soil properties from new spectral readings. To reduce the complexity of a calibration dataset derived from the Chinese vis–NIR soil spectral library (CSSL), we tested a local regression method that combined geographical sub‐setting with a local partial least squares regression (local‐PLSR) that uses a limited number of similar vis–NIR spectra (k‐nearest neighbours). The central idea of the local regression, and of other local statistical approaches, is to derive a local prediction model by identifying samples in the calibration dataset that are similar, in spectral variable space, to the samples used for prediction. Here, to derive our local regressions we used Euclidean distance in spectral space between the calibration dataset and prediction samples, and we also used soil geographical zoning to account for similarities in soil‐forming conditions. We tested this approach with the CSSL, which comprised 2732 soil samples collected from 20 provinces in the People's Republic of China to predict soil organic matter (SOM). Results showed that the prediction accuracy of our spatially constrained local‐PLSR method (R² = 0.74, RPIQ = 2.6) was better than that from local‐PLSR (R² = 0.69, RPIQ = 2.3) and PLSR alone (R² = 0.50, RPIQ = 1.5). The coupling of a local‐PLSR regression with soil geographical zoning can improve the accuracy of local SOM predictions using large, complex soil spectral libraries. The approach might be embedded into vis–NIR sensors for laboratory analysis or field estimation.     

Residue incorporation mitigates tillage‐induced loss of soil carbon in laboratory microcosms

Annual horticultural systems rely on frequent and intensive tillage to prepare beds, manage weeds and control insects. But this practice reduces soil organic carbon (SOC) through accelerated CO₂ emission. Crop residue incorporation could counteract this loss. We investigated whether vegetable systems could be made more resilient by including a high‐residue grain crop such as sweet corn (Zea mays L. var. rugosa), in the rotation through the use of conventional (no residue, no soil sieving) and organic (residue incorporated and soil sieved) soil management scenarios. We evaluated short‐term emission of CO₂‐C and soil C content in incubated Chromosol and Vertosol soils (Australian Classification) with and without sieving (simulated tillage) or the incorporation of ground sweet corn residue. Residue treatment emitted 2.3 times more CO₂‐C compared to the no‐residue treatment, and furthermore, sieved soil emitted 1.5 times more CO₂‐C than the unsieved across the two soil types. The residue incorporation had a greater effect on CO₂‐C flux than simulated tillage, suggesting that C availability and form can be more important than physical disturbance in cropping soils. The organic scenario (with residue and sieved) emitted more CO₂‐C, but had 13% more SOC compared with the conventional scenario (without residue and unsieved), indicating that organic systems may retain more SOC than a conventional system. The SOC lost by soil disturbance was more than offset by the incorporation of residue in the laboratory conditions. Therefore, the possible SOC loss by tillage for weed control under organic management may be offset by organic residue input.     

An improved method for measurement of soil aggregate stability using laser granulometry applied at regional scale

Laboratory‐based aggregate stability (AS) tests should be applied to material wetted to a moisture content comparable with that of a field soil. We have improved our original laser granulometer (LG)‐based AS test published in this journal by including a pre‐wetting stage. Our method estimates disaggregation reduction (DR; µm) for a soil sample (1–2‐mm diameter aggregates). Soils with more stable aggregates have larger DR values. We apply the new technique to soils from 60 cultivated sites across eastern England, with ten samples from each of six different parent material (PM) types encompassing a wide range of soil organic carbon (SOC) concentrations (1.2–7.0%). There are large differences between the median DR values (rescaled to < 500 µm) for soils over the PM types, which when used as a predictor (in combination with SOC concentration) accounted for 53% of the variation in DR. There was no evidence for including an interaction term between PM class and SOC concentration for the prediction of DR. After applying the aggregate stability tests with the 60 regional soil samples, they were stored for 9 months and the tests were repeated, resulting in a small but statistically significant increase in DR for samples from some, but not all, PM types. We show how a palaeosol excavated from a site in southern England can be used as an aggregate reference material (RM) to monitor the reproducibility of our technique. It has been suggested that soil quality, measured by critical soil physical properties, may decline if the organic carbon concentration is less than a critical threshold. Our results show that, for aggregate stability, any such thresholds are specific to the PM.     

Methods to Estimate the Protection of Soil Organic Carbon within Macroaggregates, 1: Does Soil Water Status Affect the Estimated Amount of Soil Organic Carbon Protected inside Macroaggregates?

The additional mineralized soil organic carbon (SOC) after soil crushing is considered to be the amount of SOC protected within aggregates (>200 μm). This study investigated the effect of soil moisture in crushed and uncrushed soil samples on the calculated amounts of protected SOC in five tropical soils (Arenosol, two Ferralsols, Nitisol, and Vertisol). No differences in soil moisture optimum were observed between crushed and uncrushed soil samples, except in clayey soils with high SOC contents and high SOC mineralization rates (Nitisol and Vertisol). Crushing the soil increased soil respiration by 0.9 to 2.4 times. Soil moisture seemed to be a confounding factor in estimation of the SOC-protected amount only in soil with a high amount of protected SOC or with a low macroaggregate stability (Ferralsol and Vertisol). In these soils, the amount of protected SOC could be influenced by the method used to estimate it.     

The use of visible and near‐infrared spectroscopy for the analysis of soil water repellency

This study investigated the potential of visible/near‐infrared reflectance spectroscopy (Vis‐NIRS) to predict soil water repellency (SWR). The top 40 mm of soils (n = 288) across 48 sites under pastoral land‐use in the North Island of New Zealand, which represented 10 soil orders and covered five classes of drought proneness, were analysed by standard laboratory methods and Vis‐NIRS. Soil WR was measured by using the molarity of ethanol droplet (MED) and the water drop penetration time (WDPT) tests. Soil organic carbon content (%C) was also measured to examine a possible relationship with SWR. A partial least squares regression (PLSR) model was developed by using Vis‐NIRS spectral data and the reference laboratory data. In addition, we explored the power of discrimination based on WDPT classes using partial least squares discriminant analysis (PLS‐DA). The PLSR of the processed spectra produced moderately accurate prediction for MED (R²_val = 0.61, RPD_val = 1.60, RMSE_val = 0.59) and good prediction for %C (R²_val = 0.82, RPD_val = 2.30, RMSE_val = 2.72). When the data from the 10 soil orders were considered separately and based on soil order rather than being grouped, the prediction of MED was further improved except for the Allophanic, Brown, Organic and Ultic soil orders. The PLS‐DA was successful in classifying 60% of soil samples into the correct WDPT classes. Our results indicate clearly that Vis‐NIRS has the potential to predict SWR. Further improvement in the prediction accuracy of SWR is envisaged by increasing the understanding of the relationship between Vis‐NIRS and the SWR of all New Zealand soil orders as a function of their physical properties and chemical constituents such as hydrophobic compounds.