In situ and laboratory soil spectroscopy with portable visible-to-near-infrared and mid-infrared instruments for the assessment of organic carbon in soils

Geoderma ◽  
2019 ◽  
Vol 355 ◽  
pp. 113900 ◽  
Author(s):  
Christopher Hutengs ◽  
Michael Seidel ◽  
Felix Oertel ◽  
Bernard Ludwig ◽  
Michael Vohland
NIR news ◽  
2017 ◽  
Vol 28 (4) ◽  
pp. 3-5 ◽  
Author(s):  
JJ Roberts ◽  
D Cozzolino

The increasing use of hand-held or portable infrared instruments (near infrared and mid infrared (MIR)), the development of new algorithms and the increasing use of chemometrics have changed the way that infrared spectroscopy is used to measure different properties in soils, allowing the measurement of samples in the field (on-the go). However, key important aspects on the use of near infrared spectroscopy to analyse soil samples containing high moisture levels still not well understood. A brief summary of the main issues related with applications of NIR spectroscopy to measure soil samples in the field are discussed in this article.


Soil Research ◽  
2005 ◽  
Vol 43 (6) ◽  
pp. 713 ◽  
Author(s):  
Adam Pirie ◽  
Balwant Singh ◽  
Kamrunnahar Islam

Reflectance spectroscopy techniques in the ultraviolet, visible, near-infrared and mid-infrared regions are alternatives for many traditional laboratory methods for measuring soil properties. However, debate exists over whether the near-infrared (700–2500 nm) or the mid-infrared (MIR, 2500–25000 nm) region of the electromagnetic spectrum is more useful for predicting soil properties. Therefore, the aim of this study was to compare UV-VIS-NIR and MIR spectroscopic techniques to predict several soil properties. A total of 415 surface and subsurface soil samples were collected from widely spread locations within New South Wales and south-eastern Queensland of Australia to model the proposed hypothesis. Principal component regression analysis (PCR) was used to develop calibration and validation models from soil spectra and reference laboratory values. The models developed using MIR spectra achieved higher prediction accuracy (regression coefficient, r2 = 0.62–0.85) for pH, organic carbon, clay, sand, CEC, and exchangeable Ca and Mg than that obtained by UV-VIS-NIR spectra (r2 = 0.28–0.76). PCR models were also developed for the combined spectral regions (UV-VIS-NIR+MIR). The models developed using combined spectra were also found to predict pH, organic carbon, clay, sand, CEC, and exchangeable Ca and Mg with acceptable accuracy (r2 = 0.59–0.79). The results of this study indicate that MIR spectra are better than UV-VIS-NIR spectra for estimation of common soil properties.


Soil Research ◽  
2015 ◽  
Vol 53 (8) ◽  
pp. 913 ◽  
Author(s):  
F. Le Guillou ◽  
W. Wetterlind ◽  
R. A. Viscarra Rossel ◽  
W. Hicks ◽  
M. Grundy ◽  
...  

Mid-infrared (mid-IR) diffuse reflectance spectroscopy can be used to effectively analyse soil, but the preparation of soil samples by grinding is time consuming. Soil samples are usually finely ground to a particle size of less than 0.250 mm because the spectrometer’s beam aperture is approximately 1–2 mm in diameter. Larger particles can generate specular reflections and spectra that do not adequately represent the soil sample. Grinding soil to small particle sizes enables the diffuse reflectance of light and more representative sample measurements. Here, we report on research that investigates the effect that grinding to different particle sizes have on soil mid-IR spectra. Our aims were to compare the effect of grinding soil to different particle sizes (2.000 mm, 1.000 mm, 0.500 mm, 0.250 mm and 0.106 mm) on the frequencies of mid-IR spectra, and compare the effect of these particle sizes on the accuracy of spectroscopic calibrations to predict organic carbon, sand, silt and clay contents. Using the Commonwealth Scientific and Industrial Research Organisation’s (CSIRO) National visible–near infrared database, we selected 227 soil samples from the National Soil Archive for our experiments, and designed an experiment whereby each soil sample was ground in triplicate to the different particle sizes. These ground samples were measured using an FT-IR spectrometer with a spectral range of 4000–600 cm–1. Grinding to particle sizes that are ≤2.000 mm reduces subsample variability. Smaller particle sizes produce finer and sharper absorption features, which are related to organic carbon, and clay and sand mineralogies. Generally, better predictions for clay, sand and soil organic carbon contents were achieved using soil that is more finely ground, but there were no statistically significant differences between predictions that use soil ground to 1 mm, 0.5 mm, 0.25 mm. Grinding did not affect predictions of silt content. Recommendations on how much grinding is required for mid-IR analysis should also consider the time, cost and effort needed to prepare the soil samples as well as the purpose of the analysis.


2018 ◽  
Vol 11 (3) ◽  
pp. 1549-1563 ◽  
Author(s):  
David W. T. Griffith ◽  
Denis Pöhler ◽  
Stefan Schmitt ◽  
Samuel Hammer ◽  
Sanam N. Vardag ◽  
...  

Abstract. In complex and urban environments, atmospheric trace gas composition is highly variable in time and space. Point measurement techniques for trace gases with in situ instruments are well established and accurate, but do not provide spatial averaging to compare against developing high-resolution atmospheric models of composition and meteorology with resolutions of the order of a kilometre. Open-path measurement techniques provide path average concentrations and spatial averaging which, if sufficiently accurate, may be better suited to assessment and interpretation with such models. Open-path Fourier transform spectroscopy (FTS) in the mid-infrared region, and differential optical absorption spectroscopy (DOAS) in the UV and visible, have been used for many years for open-path spectroscopic measurements of selected species in both clean air and in polluted environments. Near infrared instrumentation allows measurements over longer paths than mid-infrared FTS for species such as greenhouse gases which are not easily accessible to DOAS.In this pilot study we present the first open-path near-infrared (4000–10 000 cm−1, 1.0–2.5 µm) FTS measurements of CO2, CH4, O2, H2O and HDO over a 1.5 km path in urban Heidelberg, Germany. We describe the construction of the open-path FTS system, the analysis of the collected spectra, several measures of precision and accuracy of the measurements, and the results a four-month trial measurement period in July–November 2014. The open-path measurements are compared to calibrated in situ measurements made at one end of the open path. We observe significant differences of the order of a few ppm for CO2 and a few tens of ppb for CH4 between the open-path and point measurements which are 2 to 4 times the measurement repeatability, but we cannot unequivocally assign the differences to specific local sources or sinks. We conclude that open-path FTS may provide a valuable new tool for investigations of atmospheric trace gas composition in complex, small-scale environments such as cities.


2022 ◽  
Vol 217 ◽  
pp. 105284
Author(s):  
Yongsheng Hong ◽  
Muhammad Abdul Munnaf ◽  
Angela Guerrero ◽  
Songchao Chen ◽  
Yaolin Liu ◽  
...  

2017 ◽  
Author(s):  
David W. T. Griffith ◽  
Denis Pöhler ◽  
Stefan Schmitt ◽  
Samuel Hammer ◽  
Sanam N. Vardag ◽  
...  

Abstract. In complex and urban environments, atmospheric trace gas composition is highly variable in time and space. Point measurement techniques for trace gases with in situ instruments are well established and accurate, but do not provide spatial averaging to compare against developing high resolution atmospheric models of composition and small scale meteorology with resolutions of the order of a kilometre. Open path measurement techniques provide path average concentrations and spatial averaging which, if sufficiently accurate, may be better suited to assessment and interpretation with such models. Open path Fourier Transform Spectroscopy (FTS) in the mid infrared region, and Differential Optical Absorption Spectroscopy (DOAS) in the UV and visible, have been used for many years for open path spectroscopic measurements of selected species in both clean air and in polluted environments. Compared to the mid infrared, near infrared instrumentation allows measurements over longer paths than mid IR FTS, for species such as greenhouse gases which are not easily accessible to DOAS. In this pilot study we present the first open path near infrared (4000–10 000 cm−1, 1.0–2.5 μm) FTS measurements of CO2, CH4, O2, H2O and HDO over a 1.5 km path in urban Heidelberg, Germany. We describe the construction of the open path FTS system, the analysis of the collected spectra, precision and accuracy of the measurements, and the results from a four-month trial measurement period in July–November 2014. The open path measurements are compared to calibrated in situ measurements made at one end of the open path. There are small but significant differences between in situ and open path measurements coincident in time which reflect local sources and sinks and the way in which they are sampled by the point and path-averaged measurements. Open path FTS may provide a valuable new tool for investigations of atmospheric trace gas composition in complex, small scale environments such as cities.


2015 ◽  
Vol 69 (6) ◽  
pp. 760-772 ◽  
Author(s):  
Kevin C. Sales ◽  
Filipa Rosa ◽  
Pedro N. Sampaio ◽  
Luís P. Fonseca ◽  
Marta B. Lopes ◽  
...  

2019 ◽  
Author(s):  
Michael Stukel ◽  
Thomas Kelly

Thorium-234 (234Th) is a powerful tracer of particle dynamics and the biological pump in the surface ocean; however, variability in carbon:thorium ratios of sinking particles adds substantial uncertainty to estimates of organic carbon export. We coupled a mechanistic thorium sorption and desorption model to a one-dimensional particle sinking model that uses realistic particle settling velocity spectra. The model generates estimates of 238U-234Th disequilibrium, particulate organic carbon concentration, and the C:234Th ratio of sinking particles, which are then compared to in situ measurements from quasi-Lagrangian studies conducted on six cruises in the California Current Ecosystem. Broad patterns observed in in situ measurements, including decreasing C:234Th ratios with depth and a strong correlation between sinking C:234Th and the ratio of vertically-integrated particulate organic carbon (POC) to vertically-integrated total water column 234Th, were accurately recovered by models assuming either a power law distribution of sinking speeds or a double log normal distribution of sinking speeds. Simulations suggested that the observed decrease in C:234Th with depth may be driven by preferential remineralization of carbon by particle-attached microbes. However, an alternate model structure featuring complete consumption and/or disaggregation of particles by mesozooplankton (e.g. no preferential remineralization of carbon) was also able to simulate decreasing C:234Th with depth (although the decrease was weaker), driven by 234Th adsorption onto slowly sinking particles. Model results also suggest that during bloom decays C:234Th ratios of sinking particles should be higher than expected (based on contemporaneous water column POC), because high settling velocities minimize carbon remineralization during sinking.


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