Articles | Volume 6, issue 1
https://doi.org/10.5194/soil-6-17-2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/soil-6-17-2020
© Author(s) 2020. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Identification of new microbial functional standards for soil quality assessment
Universität Trier, Bodenkunde, Behringstr. 21, 54286 Trier,
Germany
Michael Schloter
Helmholtz Zentrum München, Deutsches Forschungszentrum für
Gesundheit und Umwelt, Abteilung für vergleichende Mikrobiomanalysen,
Ingolstädter Landstr. 1, 85764 Neuherberg, Germany
Berndt-Michael Wilke
TU Berlin, FG Bodenkunde, Ernst-Reuter-Platz 1, 10587 Berlin, Germany
Lee A. Beaudette
Environment and Climate Change Canada, 335 River Road, Ottawa,
Ontario, K1A 0H3, Canada
Fabrice Martin-Laurent
AgroSup Dijon, INRA, Université Bourgogne, Université
Bourgogne Franche-Comté, Agroécologie, 17 rue Sully, 21065 Dijon
CÉDEX, France
Nathalie Cheviron
UMR ECOSYS, Platform Biochem-Env, INRA, AgroParisTech, Université
Paris-Saclay, 78026, Versailles, France
Christian Mougin
UMR ECOSYS, Platform Biochem-Env, INRA, AgroParisTech, Université
Paris-Saclay, 78026, Versailles, France
Jörg Römbke
ECT Oekotoxikologie GmbH, Böttgerstr. 2–14, 65439 Flörsheim,
Germany
Related authors
Malte Ortner, Michael Seidel, Sebastian Semella, Thomas Udelhoven, Michael Vohland, and Sören Thiele-Bruhn
SOIL, 8, 113–131, https://doi.org/10.5194/soil-8-113-2022, https://doi.org/10.5194/soil-8-113-2022, 2022
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Soil organic carbon (SOC) and its labile fractions are influenced by soil use and mineral properties. These parameters interact with each other and affect SOC differently depending on local conditions. To investigate the latter, the dependence of SOC content on parameters that vary on a local scale depending on parent material, soil texture, and land use as well as parameter combinations was statistically assessed. Relevance and superiority of local models compared to total models were shown.
Björn Klaes, Rolf Kilian, Gerhard Wörner, Sören Thiele-Bruhn, and Helge W. Arz
E&G Quaternary Sci. J., 67, 1–6, https://doi.org/10.5194/egqsj-67-1-2018, https://doi.org/10.5194/egqsj-67-1-2018, 2018
Malte Ortner, Michael Seidel, Sebastian Semella, Thomas Udelhoven, Michael Vohland, and Sören Thiele-Bruhn
SOIL, 8, 113–131, https://doi.org/10.5194/soil-8-113-2022, https://doi.org/10.5194/soil-8-113-2022, 2022
Short summary
Short summary
Soil organic carbon (SOC) and its labile fractions are influenced by soil use and mineral properties. These parameters interact with each other and affect SOC differently depending on local conditions. To investigate the latter, the dependence of SOC content on parameters that vary on a local scale depending on parent material, soil texture, and land use as well as parameter combinations was statistically assessed. Relevance and superiority of local models compared to total models were shown.
Björn Klaes, Rolf Kilian, Gerhard Wörner, Sören Thiele-Bruhn, and Helge W. Arz
E&G Quaternary Sci. J., 67, 1–6, https://doi.org/10.5194/egqsj-67-1-2018, https://doi.org/10.5194/egqsj-67-1-2018, 2018
L. Fuchslueger, E.-M. Kastl, F. Bauer, S. Kienzl, R. Hasibeder, T. Ladreiter-Knauss, M. Schmitt, M. Bahn, M. Schloter, A. Richter, and U. Szukics
Biogeosciences, 11, 6003–6015, https://doi.org/10.5194/bg-11-6003-2014, https://doi.org/10.5194/bg-11-6003-2014, 2014
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In mountain grasslands drought has distinct transient effects on soil nitrogen cycling and bacterial and archaeal ammonia-oxidizers (AOB and AOA), which could have been related to a niche differentiation of these two groups at increasing NH4+ levels. However, the effective strength of drought was modulated by the level of grassland management.
J. Esperschütz, C. Zimmermann, A. Dümig, G. Welzl, F. Buegger, M. Elmer, J. C. Munch, and M. Schloter
Biogeosciences, 10, 5115–5124, https://doi.org/10.5194/bg-10-5115-2013, https://doi.org/10.5194/bg-10-5115-2013, 2013
S. Schulz, R. Brankatschk, A. Dümig, I. Kögel-Knabner, M. Schloter, and J. Zeyer
Biogeosciences, 10, 3983–3996, https://doi.org/10.5194/bg-10-3983-2013, https://doi.org/10.5194/bg-10-3983-2013, 2013
S. Schulz, M. Engel, D. Fischer, F. Buegger, M. Elmer, G. Welzl, and M. Schloter
Biogeosciences, 10, 1183–1192, https://doi.org/10.5194/bg-10-1183-2013, https://doi.org/10.5194/bg-10-1183-2013, 2013
Related subject area
Soil and methods
Spatial prediction of organic carbon in German agricultural topsoil using machine learning algorithms
On the benefits of clustering approaches in digital soil mapping: an application example concerning soil texture regionalization
An open Soil Structure Library based on X-ray CT data
Identification of thermal signature and quantification of charcoal in soil using differential scanning calorimetry and benzene polycarboxylic acid (BPCA) markers
Estimating soil fungal abundance and diversity at a macroecological scale with deep learning spectrotransfer functions
An underground, wireless, open-source, low-cost system for monitoring oxygen, temperature, and soil moisture
Estimation of soil properties with mid-infrared soil spectroscopy across yam production landscapes in West Africa
The central African soil spectral library: a new soil infrared repository and a geographical prediction analysis
Developing the Swiss mid-infrared soil spectral library for local estimation and monitoring
Predicting the spatial distribution of soil organic carbon stock in Swedish forests using a group of covariates and site-specific data
Improved calibration of the Green–Ampt infiltration module in the EROSION-2D/3D model using a rainfall-runoff experiment database
Quantifying soil carbon in temperate peatlands using a mid-IR soil spectral library
Are researchers following best storage practices for measuring soil biochemical properties?
Quantifying and correcting for pre-assay CO2 loss in short-term carbon mineralization assays
The influence of training sample size on the accuracy of deep learning models for the prediction of soil properties with near-infrared spectroscopy data
Game theory interpretation of digital soil mapping convolutional neural networks
Comparing three approaches of spatial disaggregation of legacy soil maps based on the Disaggregation and Harmonisation of Soil Map Units Through Resampled Classification Trees (DSMART) algorithm
Oblique geographic coordinates as covariates for digital soil mapping
Development of pedotransfer functions for water retention in tropical mountain soil landscapes: spotlight on parameter tuning in machine learning
The 15N gas-flux method to determine N2 flux: a comparison of different tracer addition approaches
A new model for intra- and inter-institutional soil data sharing
Machine learning and soil sciences: a review aided by machine learning tools
Identifying and quantifying geogenic organic carbon in soils – the case of graphite
Error propagation in spectrometric functions of soil organic carbon
Word embeddings for application in geosciences: development, evaluation, and examples of soil-related concepts
Soil lacquer peel do-it-yourself: simply capturing beauty
Multi-source data integration for soil mapping using deep learning
Using deep learning for digital soil mapping
No silver bullet for digital soil mapping: country-specific soil organic carbon estimates across Latin America
Separation of soil respiration: a site-specific comparison of partition methods
Proximal sensing for soil carbon accounting
Evaluation of digital soil mapping approaches with large sets of environmental covariates
Planning spatial sampling of the soil from an uncertain reconnaissance variogram
Mapping of soil properties at high resolution in Switzerland using boosted geoadditive models
Quantitative imaging of the 3-D distribution of cation adsorption sites in undisturbed soil
Decision support for the selection of reference sites using 137Cs as a soil erosion tracer
Soil organic carbon stocks are systematically overestimated by misuse of the parameters bulk density and rock fragment content
The added value of biomarker analysis to the genesis of plaggic Anthrosols; the identification of stable fillings used for the production of plaggic manure
Synchrotron microtomographic quantification of geometrical soil pore characteristics affected by compaction
Pedotransfer functions for Irish soils – estimation of bulk density (ρb) per horizon type
Assessing the performance of a plastic optical fibre turbidity sensor for measuring post-fire erosion from plot to catchment scale
Passive soil heating using an inexpensive infrared mirror design – a proof of concept
The application of terrestrial laser scanner and SfM photogrammetry in measuring erosion and deposition processes in two opposite slopes in a humid badlands area (central Spanish Pyrenees)
Soil surface roughness: comparing old and new measuring methods and application in a soil erosion model
Comparison of spatial association approaches for landscape mapping of soil organic carbon stocks
Eddy covariance for quantifying trace gas fluxes from soils
Ali Sakhaee, Anika Gebauer, Mareike Ließ, and Axel Don
SOIL, 8, 587–604, https://doi.org/10.5194/soil-8-587-2022, https://doi.org/10.5194/soil-8-587-2022, 2022
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As soil carbon has become a key component of climate-smart agriculture, the demand for high-resolution maps has increased drastically. Meanwhile, machine learning algorithms are becoming more widely used and are opening up new solutions in soil mapping. This paper shows which algorithms perform best, how soil inventory data can be most efficiently used for digital soil mapping, and the different available options and methods to derive high-resolution soil carbon data at the large regional scale.
István Dunkl and Mareike Ließ
SOIL, 8, 541–558, https://doi.org/10.5194/soil-8-541-2022, https://doi.org/10.5194/soil-8-541-2022, 2022
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Digital soil mapping (DSM) allows us to regionalize soil properties by relating them to environmental covariates with the help of an empirical model. Legacy soil data provide a valuable basis to generate high-resolution soil maps with DSM. We studied the usefulness of data-clustering methods to tackle potential sampling bias in legacy soil data while applying DSM for soil texture regionalization. Clustering has proved to be useful in various steps of the DSM process.
Ulrich Weller, Lukas Albrecht, Steffen Schlüter, and Hans-Jörg Vogel
SOIL, 8, 507–515, https://doi.org/10.5194/soil-8-507-2022, https://doi.org/10.5194/soil-8-507-2022, 2022
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Soil structure is of central importance for soil functions. It is, however, ill defined. With the increasing availability of X-ray CT scanners, more and more soils are scanned and an undisturbed image of the soil's structure is produced. Often, a qualitative description is all that is derived from these images. We provide now a web-based Soil Structure Library where these images can be evaluated in a standardized quantitative way and can be compared to a world-wide data set.
Brieuc Hardy, Nils Borchard, and Jens Leifeld
SOIL, 8, 451–466, https://doi.org/10.5194/soil-8-451-2022, https://doi.org/10.5194/soil-8-451-2022, 2022
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Soil amendment with artificial black carbon (BC; biomass transformed by incomplete combustion) has the potential to mitigate climate change. Nevertheless, the accurate quantification of BC in soil remains a critical issue. Here, we successfully used dynamic thermal analysis (DTA) to quantify centennial BC in soil. We demonstrate that DTA is largely under-exploited despite providing rapid and low-cost quantitative information over the range of soil organic matter.
Yuanyuan Yang, Zefang Shen, Andrew Bissett, and Raphael A. Viscarra Rossel
SOIL, 8, 223–235, https://doi.org/10.5194/soil-8-223-2022, https://doi.org/10.5194/soil-8-223-2022, 2022
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We present a new method to estimate the relative abundance of the dominant phyla and diversity of fungi in Australian soil. It uses state-of-the-art machine learning with publicly available data on soil and environmental proxies for edaphic, climatic, biotic and topographic factors, and visible–near infrared wavelengths. The estimates could serve to supplement the more expensive molecular approaches towards a better understanding of soil fungal abundance and diversity in agronomy and ecology.
Elad Levintal, Yonatan Ganot, Gail Taylor, Peter Freer-Smith, Kosana Suvocarev, and Helen E. Dahlke
SOIL, 8, 85–97, https://doi.org/10.5194/soil-8-85-2022, https://doi.org/10.5194/soil-8-85-2022, 2022
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Do-it-yourself hardware is a new approach for improving measurement resolution in research. Here we present a new low-cost, wireless underground sensor network for soil monitoring. All data logging, power, and communication component cost is USD 150, much cheaper than other available commercial solutions. We provide the complete building guide to reduce any technical barriers, which we hope will allow easier reproducibility and open new environmental monitoring applications.
Philipp Baumann, Juhwan Lee, Emmanuel Frossard, Laurie Paule Schönholzer, Lucien Diby, Valérie Kouamé Hgaza, Delwende Innocent Kiba, Andrew Sila, Keith Sheperd, and Johan Six
SOIL, 7, 717–731, https://doi.org/10.5194/soil-7-717-2021, https://doi.org/10.5194/soil-7-717-2021, 2021
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This work delivers openly accessible and validated calibrations for diagnosing 26 soil properties based on mid-infrared spectroscopy. These were developed for four regions in Burkina Faso and Côte d'Ivoire, including 80 fields of smallholder farmers. The models can help to site-specifically and cost-efficiently monitor soil quality and fertility constraints to ameliorate soils and yields of yam or other staple crops in the four regions between the humid forest and the northern Guinean savanna.
Laura Summerauer, Philipp Baumann, Leonardo Ramirez-Lopez, Matti Barthel, Marijn Bauters, Benjamin Bukombe, Mario Reichenbach, Pascal Boeckx, Elizabeth Kearsley, Kristof Van Oost, Bernard Vanlauwe, Dieudonné Chiragaga, Aimé Bisimwa Heri-Kazi, Pieter Moonen, Andrew Sila, Keith Shepherd, Basile Bazirake Mujinya, Eric Van Ranst, Geert Baert, Sebastian Doetterl, and Johan Six
SOIL, 7, 693–715, https://doi.org/10.5194/soil-7-693-2021, https://doi.org/10.5194/soil-7-693-2021, 2021
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We present a soil mid-infrared library with over 1800 samples from central Africa in order to facilitate soil analyses of this highly understudied yet critical area. Together with an existing continental library, we demonstrate a regional analysis and geographical extrapolation to predict total carbon and nitrogen. Our results show accurate predictions and highlight the value that the data contribute to existing libraries. Our library is openly available for public use and for expansion.
Philipp Baumann, Anatol Helfenstein, Andreas Gubler, Armin Keller, Reto Giulio Meuli, Daniel Wächter, Juhwan Lee, Raphael Viscarra Rossel, and Johan Six
SOIL, 7, 525–546, https://doi.org/10.5194/soil-7-525-2021, https://doi.org/10.5194/soil-7-525-2021, 2021
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We developed the Swiss mid-infrared spectral library and a statistical model collection across 4374 soil samples with reference measurements of 16 properties. Our library incorporates soil from 1094 grid locations and 71 long-term monitoring sites. This work confirms once again that nationwide spectral libraries with diverse soils can reliably feed information to a fast chemical diagnosis. Our data-driven reduction of the library has the potential to accurately monitor carbon at the plot scale.
Kpade O. L. Hounkpatin, Johan Stendahl, Mattias Lundblad, and Erik Karltun
SOIL, 7, 377–398, https://doi.org/10.5194/soil-7-377-2021, https://doi.org/10.5194/soil-7-377-2021, 2021
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Forests store large amounts of carbon in soils. Implementing suitable measures to improve the sink potential of forest soils would require accurate data on the carbon stored in forest soils and a better understanding of the factors affecting this storage. This study showed that the prediction of soil carbon stock in Swedish forest soils can increase in accuracy when one divides a big region into smaller areas in combination with information collected locally and derived from satellites.
Hana Beitlerová, Jonas Lenz, Jan Devátý, Martin Mistr, Jiří Kapička, Arno Buchholz, Ilona Gerndtová, and Anne Routschek
SOIL, 7, 241–253, https://doi.org/10.5194/soil-7-241-2021, https://doi.org/10.5194/soil-7-241-2021, 2021
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This study presents transfer functions for a calibration parameter of the Green–Ampt infiltration module of the EROSION-2D/3D model, which are significantly improving the model performance compared to the current state. The relationships found between calibration parameters and soil parameters however put the Green–Ampt implementation in the model and the state-of-the-art parametrization method in question. A new direction of the infiltration module development is proposed.
Anatol Helfenstein, Philipp Baumann, Raphael Viscarra Rossel, Andreas Gubler, Stefan Oechslin, and Johan Six
SOIL, 7, 193–215, https://doi.org/10.5194/soil-7-193-2021, https://doi.org/10.5194/soil-7-193-2021, 2021
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In this study, we show that a soil spectral library (SSL) can be used to predict soil carbon at new and very different locations. The importance of this finding is that it requires less time-consuming lab work than calibrating a new model for every local application, while still remaining similar to or more accurate than local models. Furthermore, we show that this method even works for predicting (drained) peat soils, using a SSL with mostly mineral soils containing much less soil carbon.
Jennifer M. Rhymes, Irene Cordero, Mathilde Chomel, Jocelyn M. Lavallee, Angela L. Straathof, Deborah Ashworth, Holly Langridge, Marina Semchenko, Franciska T. de Vries, David Johnson, and Richard D. Bardgett
SOIL, 7, 95–106, https://doi.org/10.5194/soil-7-95-2021, https://doi.org/10.5194/soil-7-95-2021, 2021
Matthew A. Belanger, Carmella Vizza, G. Philip Robertson, and Sarah S. Roley
SOIL, 7, 47–52, https://doi.org/10.5194/soil-7-47-2021, https://doi.org/10.5194/soil-7-47-2021, 2021
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Soil health is often assessed by re-wetting a dry soil and measuring CO2 production, but the potential bias introduced by soils of different moisture contents is unclear. Our study found that wetter soil tended to lose more carbon during drying than drier soil, thus affecting soil health interpretations. We developed a correction factor to account for initial soil moisture effects, which future studies may benefit from adapting for their soil.
Wartini Ng, Budiman Minasny, Wanderson de Sousa Mendes, and José Alexandre Melo Demattê
SOIL, 6, 565–578, https://doi.org/10.5194/soil-6-565-2020, https://doi.org/10.5194/soil-6-565-2020, 2020
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The number of samples utilised to create predictive models affected model performance. This research compares the number of samples needed by a deep learning model to outperform the traditional machine learning models using visible near-infrared spectroscopy data for soil properties predictions. The deep learning model was found to outperform machine learning models when the sample size was above 2000.
José Padarian, Alex B. McBratney, and Budiman Minasny
SOIL, 6, 389–397, https://doi.org/10.5194/soil-6-389-2020, https://doi.org/10.5194/soil-6-389-2020, 2020
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In this paper we introduce the use of game theory to interpret a digital soil mapping (DSM) model to understand the contribution of environmental factors to the prediction of soil organic carbon (SOC) in Chile. The analysis corroborated that the SOC model is capturing sensible relationships between SOC and climatic and topographical factors. We were able to represent them spatially (map) addressing the limitations of the current interpretation of models in DSM.
Yosra Ellili-Bargaoui, Brendan Philip Malone, Didier Michot, Budiman Minasny, Sébastien Vincent, Christian Walter, and Blandine Lemercier
SOIL, 6, 371–388, https://doi.org/10.5194/soil-6-371-2020, https://doi.org/10.5194/soil-6-371-2020, 2020
Anders Bjørn Møller, Amélie Marie Beucher, Nastaran Pouladi, and Mogens Humlekrog Greve
SOIL, 6, 269–289, https://doi.org/10.5194/soil-6-269-2020, https://doi.org/10.5194/soil-6-269-2020, 2020
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Decision trees have become a widely adapted tool for mapping soil properties in geographic space. However, it is problematic to implement spatial relationships in the models. We present a new method which uses geographic coordinates along several axes tilted at oblique angles in the models. We test this method on four spatial datasets. The results show that the new method is at least as accurate as other proposed alternatives, has a computational advantage and is flexible and interpretable.
Anika Gebauer, Monja Ellinger, Victor M. Brito Gomez, and Mareike Ließ
SOIL, 6, 215–229, https://doi.org/10.5194/soil-6-215-2020, https://doi.org/10.5194/soil-6-215-2020, 2020
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Pedotransfer functions (PTFs) for soil water retention were developed for two tropical soil landscapes using machine learning. The models corresponding to these PTFs had to be adjusted by tuning their parameters. The standard tuning approach was compared to mathematical optimization. The latter resulted in much better model performance. The PTFs derived are of particular importance for soil process and hydrological models.
Dominika Lewicka-Szczebak and Reinhard Well
SOIL, 6, 145–152, https://doi.org/10.5194/soil-6-145-2020, https://doi.org/10.5194/soil-6-145-2020, 2020
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This study aimed at comparison of various experimental strategies for incubating soil samples to determine the N2 flux. Such experiments require addition of isotope tracer, i.e. nitrogen fertilizer enriched in heavy nitrogen isotopes (15N). Here we compared the impact of soil homogenization and mixing with the tracer and tracer injection to the intact soil cores. The results are well comparable: both techniques would provide similar conclusions on the magnitude of N2 flux.
José Padarian and Alex B. McBratney
SOIL, 6, 89–94, https://doi.org/10.5194/soil-6-89-2020, https://doi.org/10.5194/soil-6-89-2020, 2020
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Data sharing and collaboration are critical to solving large-scale problems. The prevailing soil data-sharing model is of a centralized nature and, consequently, results in the participants ceding control and governance over their data to the lead party. Here we explore the use of a distributed ledger (blockchain) to solve the aforementioned issues. We also describe the potential use case of developing a global soil spectral library between multiple, international institutions.
José Padarian, Budiman Minasny, and Alex B. McBratney
SOIL, 6, 35–52, https://doi.org/10.5194/soil-6-35-2020, https://doi.org/10.5194/soil-6-35-2020, 2020
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The application of machine learning (ML) has shown an accelerated adoption in soil sciences. It is a difficult task to manually review all papers on the application of ML. This paper aims to provide a review of the application of ML aided by topic modelling in order to find patterns in a large collection of publications. The objective is to gain insight into the applications and to discuss research gaps. We found 12 main topics and that ML methods usually perform better than traditional ones.
Jeroen H. T. Zethof, Martin Leue, Cordula Vogel, Shane W. Stoner, and Karsten Kalbitz
SOIL, 5, 383–398, https://doi.org/10.5194/soil-5-383-2019, https://doi.org/10.5194/soil-5-383-2019, 2019
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A widely overlooked source of carbon (C) in the soil environment is organic C of geogenic origin, e.g. graphite. Appropriate methods are not available to quantify graphite and to differentiate it from other organic and inorganic C sources in soils. Therefore, we examined Fourier transform infrared spectroscopy, thermogravimetric analysis and the smart combustion method for their ability to identify and quantify graphitic C in soils. The smart combustion method showed the most promising results.
Monja Ellinger, Ines Merbach, Ulrike Werban, and Mareike Ließ
SOIL, 5, 275–288, https://doi.org/10.5194/soil-5-275-2019, https://doi.org/10.5194/soil-5-275-2019, 2019
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Vis–NIR spectrometry is often applied to capture soil organic carbon (SOC). This study addresses the impact of the involved data and modelling aspects on SOC precision with a focus on the propagation of input data uncertainties. It emphasizes the necessity of transparent documentation of the measurement protocol and the model building and validation procedure. Particularly, when Vis–NIR spectrometry is used for soil monitoring, the aspect of uncertainty propagation becomes essential.
José Padarian and Ignacio Fuentes
SOIL, 5, 177–187, https://doi.org/10.5194/soil-5-177-2019, https://doi.org/10.5194/soil-5-177-2019, 2019
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A large amount of descriptive information is available in geosciences. Considering the advances in natural language it is possible to
rescuethis information and transform it into a numerical form (embeddings). We used 280764 full-text scientific articles to train a language model capable of generating such embeddings. Our domain-specific embeddings (GeoVec) outperformed general domain embedding tasks such as analogies, relatedness, and categorisation, and can be used in novel applications.
Cathelijne R. Stoof, Jasper H. J. Candel, Laszlo A. G. M. van der Wal, and Gert Peek
SOIL, 5, 159–175, https://doi.org/10.5194/soil-5-159-2019, https://doi.org/10.5194/soil-5-159-2019, 2019
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Teaching and outreach of soils is often done with real-life snapshots of soils and sediments in lacquer or glue peels. While it may seem hard, anyone can make such a peel. Illustrated with handmade drawings and an instructional video, we explain how to capture soils in peels using readily available materials. A new twist to old methods makes this safer, simpler, and more successful, and thus a true DIY (do-it-yourself) activity, highlighting the value and beauty of the ground below our feet.
Alexandre M. J.-C. Wadoux, José Padarian, and Budiman Minasny
SOIL, 5, 107–119, https://doi.org/10.5194/soil-5-107-2019, https://doi.org/10.5194/soil-5-107-2019, 2019
José Padarian, Budiman Minasny, and Alex B. McBratney
SOIL, 5, 79–89, https://doi.org/10.5194/soil-5-79-2019, https://doi.org/10.5194/soil-5-79-2019, 2019
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Digital soil mapping has been widely used as a cost-effective method for generating soil maps. DSM models are usually calibrated using point observations and rarely incorporate contextual information of the landscape. Here, we use convolutional neural networks to incorporate spatial context. We used as input a 3-D stack of covariate images to simultaneously predict organic carbon content at multiple depths. In this study, our model reduced the error by 30 % compared with conventional techniques.
Mario Guevara, Guillermo Federico Olmedo, Emma Stell, Yusuf Yigini, Yameli Aguilar Duarte, Carlos Arellano Hernández, Gloria E. Arévalo, Carlos Eduardo Arroyo-Cruz, Adriana Bolivar, Sally Bunning, Nelson Bustamante Cañas, Carlos Omar Cruz-Gaistardo, Fabian Davila, Martin Dell Acqua, Arnulfo Encina, Hernán Figueredo Tacona, Fernando Fontes, José Antonio Hernández Herrera, Alejandro Roberto Ibelles Navarro, Veronica Loayza, Alexandra M. Manueles, Fernando Mendoza Jara, Carolina Olivera, Rodrigo Osorio Hermosilla, Gonzalo Pereira, Pablo Prieto, Iván Alexis Ramos, Juan Carlos Rey Brina, Rafael Rivera, Javier Rodríguez-Rodríguez, Ronald Roopnarine, Albán Rosales Ibarra, Kenset Amaury Rosales Riveiro, Guillermo Andrés Schulz, Adrian Spence, Gustavo M. Vasques, Ronald R. Vargas, and Rodrigo Vargas
SOIL, 4, 173–193, https://doi.org/10.5194/soil-4-173-2018, https://doi.org/10.5194/soil-4-173-2018, 2018
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We provide a reproducible multi-modeling approach for SOC mapping across Latin America on a country-specific basis as required by the Global Soil Partnership of the United Nations. We identify key prediction factors for SOC across each country. We compare and test different methods to generate spatially explicit predictions of SOC and conclude that there is no best method on a quantifiable basis.
Louis-Pierre Comeau, Derrick Y. F. Lai, Jane Jinglan Cui, and Jenny Farmer
SOIL, 4, 141–152, https://doi.org/10.5194/soil-4-141-2018, https://doi.org/10.5194/soil-4-141-2018, 2018
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To date, there are still many uncertainties and unknowns regarding the soil respiration partitioning procedures. This study compared the suitability and accuracy of five different respiration partitioning methods. A qualitative evaluation table of the partition methods with five performance parameters was produced. Overall, no systematically superior or inferior partition method was found and the combination of two or more methods optimizes assessment reliability.
Jacqueline R. England and Raphael A. Viscarra Rossel
SOIL, 4, 101–122, https://doi.org/10.5194/soil-4-101-2018, https://doi.org/10.5194/soil-4-101-2018, 2018
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Proximal sensing can be used for soil C accounting, but the methods need to be standardized and procedural guidelines developed to ensure proficient measurement and accurate reporting. This is particularly important if there are financial incentives for landholders to adopt practices to sequester C. We review sensing for C accounting and discuss the requirements for the development of new soil C accounting methods based on sensing, including requirements for reporting, auditing and verification.
Madlene Nussbaum, Kay Spiess, Andri Baltensweiler, Urs Grob, Armin Keller, Lucie Greiner, Michael E. Schaepman, and Andreas Papritz
SOIL, 4, 1–22, https://doi.org/10.5194/soil-4-1-2018, https://doi.org/10.5194/soil-4-1-2018, 2018
Short summary
Short summary
This paper presents an extensive evaluation of digital soil mapping (DSM) tools. Recently, large sets of environmental covariates (e.g. from analysis of terrain on multiple scales) have become more common for DSM. Many DSM studies, however, only compared DSM methods using less than 30 covariates or tested approaches on few responses. We built DSM models from 300–500 covariates using six approaches that are either popular in DSM or promising for large covariate sets.
R. Murray Lark, Elliott M. Hamilton, Belinda Kaninga, Kakoma K. Maseka, Moola Mutondo, Godfrey M. Sakala, and Michael J. Watts
SOIL, 3, 235–244, https://doi.org/10.5194/soil-3-235-2017, https://doi.org/10.5194/soil-3-235-2017, 2017
Short summary
Short summary
An advantage of geostatistics for mapping soil properties is that, given a statistical model of the variable of interest, we can make a rational decision about how densely to sample so that the map is sufficiently precise. However, uncertainty about the statistical model affects this process. In this paper we show how Bayesian methods can be used to support decision making on sampling with an uncertain model, ensuring that the probability of meeting certain levels of precision is high enough.
Madlene Nussbaum, Lorenz Walthert, Marielle Fraefel, Lucie Greiner, and Andreas Papritz
SOIL, 3, 191–210, https://doi.org/10.5194/soil-3-191-2017, https://doi.org/10.5194/soil-3-191-2017, 2017
Short summary
Short summary
Digital soil mapping (DSM) relates soil property data to environmental data that describe soil-forming factors. With imagery sampled from satellites or terrain analysed at multiple scales, large sets of possible input to DSM are available. We propose a new statistical framework (geoGAM) that selects parsimonious models for DSM and illustrate the application of geoGAM to two study regions. Straightforward interpretation of the modelled effects likely improves end-user acceptance of DSM products.
Hannes Keck, Bjarne W. Strobel, Jon Petter Gustafsson, and John Koestel
SOIL, 3, 177–189, https://doi.org/10.5194/soil-3-177-2017, https://doi.org/10.5194/soil-3-177-2017, 2017
Short summary
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Several studies have shown that the cation adsorption sites in soils are heterogeneously distributed in space. In many soil system models this knowledge is not included yet. In our study we proposed a new method to map the 3-D distribution of cation adsorption sites in undisturbed soils. The method is based on three-dimensional X-ray scanning with a contrast agent and image analysis. We are convinced that this approach will strongly aid the development of more realistic soil system models.
Laura Arata, Katrin Meusburger, Alexandra Bürge, Markus Zehringer, Michael E. Ketterer, Lionel Mabit, and Christine Alewell
SOIL, 3, 113–122, https://doi.org/10.5194/soil-3-113-2017, https://doi.org/10.5194/soil-3-113-2017, 2017
Christopher Poeplau, Cora Vos, and Axel Don
SOIL, 3, 61–66, https://doi.org/10.5194/soil-3-61-2017, https://doi.org/10.5194/soil-3-61-2017, 2017
Short summary
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This paper shows that three out of four frequently used methods to calculate soil organic carbon stocks lead to systematic overestimation of those stocks. Stones, which can be assumed to be free of carbon, have to be corrected for in both bulk density and layer thickness. We used data of the German Agricultural Soil Inventory to illustrate the potential bias and suggest a unified and unbiased calculation method for stocks of soil organic carbon, which is the largest terrestrial carbon pool.
Jan M. van Mourik, Thomas V. Wagner, J. Geert de Boer, and Boris Jansen
SOIL, 2, 299–310, https://doi.org/10.5194/soil-2-299-2016, https://doi.org/10.5194/soil-2-299-2016, 2016
Ranjith P. Udawatta, Clark J. Gantzer, Stephen H. Anderson, and Shmuel Assouline
SOIL, 2, 211–220, https://doi.org/10.5194/soil-2-211-2016, https://doi.org/10.5194/soil-2-211-2016, 2016
Short summary
Short summary
Soil compaction degrades soil structure and affects water, heat, and gas exchange as well as root penetration and crop production. The objective of this study was to use X-ray computed microtomography (CMT) techniques to compare differences in geometrical soil pore parameters as influenced by compaction of two different aggregate size classes.
B. Reidy, I. Simo, P. Sills, and R. E. Creamer
SOIL, 2, 25–39, https://doi.org/10.5194/soil-2-25-2016, https://doi.org/10.5194/soil-2-25-2016, 2016
Short summary
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This study reviews pedotransfer functions from the literature for different soil and horizon types. It uses these formulae to predict bulk density (ρb) per horizon using measured data of other soil properties. These data were compared to known pb per horizon and recalibrated. These calculations were used to fill missing horizon data in the Irish soil database. This allowed the generation of a pb map to 50 cm. These pb data are at horizon level allowing more accurate estimation of C with depth.
J. J. Keizer, M. A. S. Martins, S. A. Prats, L. F. Santos, D. C. S. Vieira, R. Nogueira, and L. Bilro
SOIL, 1, 641–650, https://doi.org/10.5194/soil-1-641-2015, https://doi.org/10.5194/soil-1-641-2015, 2015
Short summary
Short summary
In this study, a novel plastic optical fibre turbidity sensor was exhaustively tested with a large set of runoff samples, mainly from a recently burnt area. The different types of samples from the distinct study sites revealed without exception an increase in normalized light loss with increasing sediment concentrations that agreed (reasonably) well with a power function. Nevertheless, sensor-based predictions of sediment concentration should ideally involve site-specific calibrations.
C. Rasmussen, R. E. Gallery, and J. S. Fehmi
SOIL, 1, 631–639, https://doi.org/10.5194/soil-1-631-2015, https://doi.org/10.5194/soil-1-631-2015, 2015
Short summary
Short summary
There is a need to understand the response of soil systems to predicted climate warming for modeling soil processes. Current experimental methods for soil warming include expensive and difficult to implement active and passive techniques. Here we test a simple, inexpensive in situ passive soil heating approach, based on easy to construct infrared mirrors that do not require automation or enclosures. Results indicated that the infrared mirrors yielded significant heating and drying of soils.
E. Nadal-Romero, J. Revuelto, P. Errea, and J. I. López-Moreno
SOIL, 1, 561–573, https://doi.org/10.5194/soil-1-561-2015, https://doi.org/10.5194/soil-1-561-2015, 2015
Short summary
Short summary
Geomatic techniques have been routinely applied in erosion studies, providing the opportunity to build high-resolution topographic models.The aim of this study is to assess and compare the functioning of terrestrial laser scanner and close range photogrammetry techniques to evaluate erosion and deposition processes in a humid badlands area.
Our results demonstrated that north slopes experienced more intense and faster dynamics than south slopes as well as the highest erosion rates.
L. M. Thomsen, J. E. M. Baartman, R. J. Barneveld, T. Starkloff, and J. Stolte
SOIL, 1, 399–410, https://doi.org/10.5194/soil-1-399-2015, https://doi.org/10.5194/soil-1-399-2015, 2015
B. A. Miller, S. Koszinski, M. Wehrhan, and M. Sommer
SOIL, 1, 217–233, https://doi.org/10.5194/soil-1-217-2015, https://doi.org/10.5194/soil-1-217-2015, 2015
Short summary
Short summary
There are many different strategies for mapping SOC, among which is to model the variables needed to calculate the SOC stock indirectly or to model the SOC stock directly. The purpose of this research was to compare these two approaches for mapping SOC stocks from multiple linear regression models applied at the landscape scale via spatial association. Although the indirect approach had greater spatial variation and higher R2 values, the direct approach had a lower total estimated error.
W. Eugster and L. Merbold
SOIL, 1, 187–205, https://doi.org/10.5194/soil-1-187-2015, https://doi.org/10.5194/soil-1-187-2015, 2015
Short summary
Short summary
The eddy covariance (EC) method has become increasingly popular in soil science. The basic concept of this method and its use in different types of experimental designs in the field are given, and we indicate where progress in advancing and extending the field of applications is made. The greatest strengths of EC measurements in soil science are (1) their uninterrupted continuous measurement of gas concentrations and fluxes and (2) spatial integration over
small-scale heterogeneity in the soil.
Cited articles
Anderson, T. H. and Domsch, K. H.: The metabolic quotient for CO2
(qCO2) as a specific activity parameter to assess the effects of
environmental conditions, such as pH, on the microbial biomass of forest
soils, Soil Biol. Biochem., 25, 393–395, https://doi.org/10.1016/0038-0717(93)90140-7, 1993.
Bååth, E.: Growth rates of bacterial communities in soils at varying
pH: A comparison of the thymidine and leucine incorporation techniques,
Microb. Ecol., 36, 316–327 https://doi.org/10.1007/s002489900118, 1998.
Bååth, E., Pettersson, M., and Söderberg, K. H.: Adaptation of a
rapid and economical microcentrifugation method to measure thymidine and
leucine incorporation by soil bacteria, Soil Biol. Biochem., 33,
1571–1574, https://doi.org/10.1016/S0038-0717(01)00073-6, 2001.
Bach, C. E., Warnock, D. D., Van Horn, D. J., Weintraub, M. N., Sinsabaugh,
R. L., Allison, S. D., and German, D. P.: Measuring phenol oxidase and
peroxidase activities with pyrogallol, l-DOPA, and ABTS: Effect of assay
conditions and soil type, Soil Biol. Biochem., 67, 183–191, 2013.
Baldrian, P.: Fungal laccases – occurrence and properties, FEMS Microbiol.
Rev., 30, 215–242, 2006.
Bastida, F., Zsolnay, A., Hernández, T., and García, C.: Past,
present and future of soil quality indices: A biological perspective,
Geoderma, 147, 159–171, https://doi.org/10.1016/j.geoderma.2008.08.007, 2008.
Bloem, J. and Breure, A. M.: Microbial indicators, in: Trace Metals and other Contaminants in the Environment, edited by: Markert, B. A., Breure, A. M., and Zechmeister, H. G., Vol. 6, Elsevier, Dordrecht, 259–282, 2003.
Beck, T. and Beck, R.: Bodenenzyme. in: Handbuch der
Bodenkunde, edited by: Blume, H.-P., Felix-Hennigsen, P.,
Frede, H.-G., Guggenberger, G., Horn, R., and Stahr, K., Wiley-VCH, Weinheim, Germany, 244 pp., 2000.
Bergkemper, F., Kublik, S., Lang, F., Krüger, J., Vestergaard, G.,
Schloter, M., and Schulz, S.: Novel oligonucleotide primers reveal a high
diversity of microbes which drive phosphorous turnover in soil, J.
Microbiol. Meth., 125, 91–97, https://doi.org/10.1016/j.mimet.2016.04.011, 2016.
Bispo, A., Cluzeau, D., Creamer, R., Dombos, M., Graefe, U., Krogh, P. H.,
Sousa, J. P., Peres, G., Rutgers, M., Winding, A., and Römbke, J.:
Indicators for monitoring soil biodiversity, Integr. Environ.
Assess., 5, 717–719, https://doi.org/10.1897/IEAM-2009-064.1, 2009.
Bockhorst, S. and Wardle, D. A.: Microclimate within litter bags of
different mesh size: Implications for the “arthropod effect” on litter
decomposition, Soil Biol. Biochem., 58, 147–152, 2013.
Bollag, J. M.: Decontaminating soil with enzymes, Environ. Sci.
Technol., 26, 1876–1881, 1992.
Bolliger, A., Nalla, A., Magid, J., de Neergaard, A., Dole Nalla, A., and
Bøg-Hansen, T. C.: Re-examining the glomalin-purity of glomalin-related
soil protein fractions through immunochemical, lectin-affinity and soil
labelling experiments, Soil Biol. Biochem., 40, 887–893, https://doi.org/10.1016/j.soilbio.2007.10.019, 2008.
Breure, A. M., De Deyn, G. B., Dominati, E., Eglin, T., Hedlund, K., Van
Orshoven, J., and Posthuma, L.: Ecosystem services: A useful concept for
soil policy making!, Curr. Opin. Env. Sust., 4,
578–585, 2012.
Brookes, P. C.: The use of microbial parameters in monitoring soil pollution
by heavy metals, Biol. Fert. Soils, 19, 269–279, https://doi.org/10.1007/BF00336094, 1995.
Brooks, J. P., Edwards, D. J., Harwich, M. D., Jr., Rivera, M. C., Fettweis,
J. M., Serrano, M. G., Reris, R. A., Sheth, N. U., Huang, B., Girerd, P.,
Strauss III, J. F., Jefferson, K. K., and Buck, G. A.: The truth about
metagenomics: Quantifying and counteracting bias in 16S rRNA studies
ecological and evolutionary microbiology, BMC Microbiol., 15, 66, https://doi.org/10.1186/s12866-015-0351-6, 2015.
Cebron, A., Norini, M. P., Beguiristain, T., and Leyval, C.: Real-time PCR
quantification of PAH-ring hydroxylating dioxygenase (PAH-RHD alpha) genes
from Gram positive and Gram-negative Bacteria in soil and sediment samples,
J. Microbiol. Meth., 73, 148–159, 2008.
Chen, X., Su, Y., He, X., Liang Y., and Wu, J.: Comparative analysis of
basidiomycetous laccase genes in forest soils reveals differences at the
cDNA and DNA levels, Plant Soil, 366, 321–331, 2013.
Creamer, R. E., Hannula, S. E., Leeuwen, J., Stone, D., Rutgers, M.,
Schmelz, R. M., Ruiter, P., Hendriksen, N., Bolger, T., Bouffaud, M. L.,
Buee, M., Carvalho, F., Costa, D., Dirilgen, T., Francisco, R., Griffiths,
B. S., Griffiths, R., Martin, F., Silva, P. D., Mendes, S., Morais, P. V.,
Pereira, C., Philippot, L., Plassart, P., Redecker, D., Römbke, J.,
Sousa, J. P., Wouterse, M., and Lemanceau, P.: Ecological network analysis
reveals the inter-connection between soil biodiversity and ecosystem
function as affected by land use across Europe, Appl. Soil Ecol., 97,
112–124, https://doi.org/10.1016/j.apsoil.2015.08.006, 2016.
Coban, H., Miltner, A., and Kästner, M.: Fate of fatty acids derived from
biogas residues in arable soil, Soil Biol. Biochem., 91, 58–64,
2015.
Dandie, C. E., Miller, M. N., Burton, D. L., Zebarth, B. J., Trevors, J. T., and
Goyer, C.: Nitric oxide reductase-targeted real-time PCR quantification of
denitrifier populations in soil, Appl. Environ. Microb., 73,
4250–4258, 2007.
De Gonzalo, G., Colpa, D. I., Habib, M. H. M., and Fraaije, M. W.: Bacterial
enzymes involved in lignin degradation, J. Biotechnol., 236,
110–119, 2016.
Edwards, I. P., Zak, D. R., Kellner, H., Eisenlord, S. D., and Pregitzer, K. S.:
Simulated atmospheric N deposition alters fungal community composition and
suppresses ligninolytic gene expression in a Northern Hardwood forest, PLoS
ONE, 6, e20421, https://doi.org/10.1371/journal.pone.0020421, 2011.
Eichlerová, I., Šnajdr, J., and Baldrian, P.: Laccase
activity in soils: Considerations for the measurement of enzyme activity,
Chemosphere, 88, 1154–1160,
https://doi.org/10.1016/j.chemosphere.2012.03.019, 2012.
El Azhari, N., Bru, D., Sarr, A., and Martin-Laurent, F.: Estimation of the
density of the protocatechuate-degrading bacterial community in soil by
real-time PCR, Eur. J. Soil Sci., 59, 665–673, 2008.
El Azhari, N., Devers-Lamrani, M., Chatagnier, G., Rouard, N., and
Martin-Laurent, F.: Molecular analysis of the catechol-degrading bacterial
community in a coal wasteland heavily contaminated with PAHs, J.
Hazard. Mater., 177, 593–601, https://doi.org/10.1016/j.jhazmat.2009.12.074, 2010.
European Commission: EU-Regulation 1107/2009/EC of the European Parliament
and the council of 21 October 2009 concerning the placing of plant
protection products on the market and repealing Council Directives
79/117/EEC and 91/414/EEC, Offic. J. Europ. Union, L 309, 1–50, 2009.
Faber, J. H., Creamer, R. E., Mulder, C., Römbke, J., Rutgers, M., Sousa,
J. P., Stone, D., and Griffiths, B. S.: The practicalities and pitfalls of
establishing a policy-relevant and cost-effective soil biological monitoring
scheme, Integr. Environ. Assess., 9, 276–284,
2013.
Feinstein, L. M., Woo, J. S., and Blackwood, C. B.: Assessment of bias
associated with incomplete extraction of microbial DNA from soil, Appl. Environ. Microb., 75, 5428–5433, https://doi.org/10.1128/AEM.00120-09,
2009.
Fish, J. A., Chai, B., Wang, Q., Sun, Y., Brown, C. T., Tiedje, J. M., and
Cole, J. R.: FunGene: The Functional Gene Pipeline and Repository, Front. Microbiol., 4, 291, https://doi.org/10.3389/fmicb.2013.00291, 2013.
Gaby, J. C. and Buckley, D. H.: A comprehensive evaluation of PCR primers to
amplify the nifH gene of nitrogenase, PLoS ONE, 7, e93883, https://doi.org/10.1371/journal.pone.0093883, 2012.
Galic, N., Schmolke, A., Forbes, V., Baveco, H., and van den Brink, P. J.: The role of ecological models in linking ecological risk assessment to
ecosystem services in agroecosystems, Sci. Total Environ., 415,
93–100, 2012.
Garland, J. L.: Analysis and interpretation of community-level physiological
profiles in microbial ecology, FEMS Microbiol. Ecol., 24, 289–300, https://doi.org/10.1016/S0168-6496(97)00061-5, 1997.
Garland, J. L. and Mills, A. L.: Classification and characterization of
heterotrophic microbial communities on the basis of patterns of
community-level sole-carbon-source utilization, Appl. Environ.
Microb., 57, 2351–2359, 1991.
Geisen, S., Briones, M. J. I., Gan, H., Behan-Pelletier, V. M., Friman, V. P.,
de Groot, G. A., Hannula, S. E., Lindo, Z., Philippot, L., Tiunov, A. V., and
Wall, D. H.: A methodological framework to embrace soil biodiversity, Soil
Biol. Biochem., 136, 107536, https://doi.org/10.1016/j.soilbio.2019.107536, 2019.
Glimm, E., Heuer, H., Engelen, B., Smalla, K., and Backhaus, H.: Statistical
comparisons of community catabolic profiles, J. Microbiol.
Meth., 30, 71–80, https://doi.org/10.1016/S0167-7012(97)00046-8, 1997.
Gomez, E., Ferreras, L., and Toresani, S.: Soil bacterial functional
diversity as influenced by organic amendment application, Bioresource
Technol., 97, 1484–1489, https://doi.org/10.1016/j.biortech.2005.06.021, 2006.
Gomiero, T.: Soil degradation, land scarcity and food security: Reviewing a
complex challenge, Sustainability, 8, 281, https://doi.org/10.3390/su8030281,
2016.
Gorfer, M., Blumhoff, M., Klaubauf, S., Urban, A., Inselsbacher, E.,
Bandian, D., Mitter, B., Sessitsch, A., Wanek, W., and Strauss, J.:
Community profiling and gene expression of fungal assimilatory nitrate
reductases in agricultural soil, ISME J., 5, 1771–1783, 2011.
Griffiths, B. S. and Philippot, L.: Insights into the resistance and
resilience of the soil microbial community, Fems Microbiol. Rev., 37,
112–129, 2013.
Guillaume, T., Maranguit, D., Murtilaksono, K., and Kuzyakov, Y.:
Sensitivity and resistance of soil fertility indicators to land-use changes:
New concept and examples from conversion of Indonesian rainforest to
plantations, Ecol. Indic., 67, 49–57, https://doi.org/10.1016/j.ecolind.2016.02.039, 2016.
Hannula, S. E. and van Veen, J. A.: Primer sets developed for functional genes reveal shifts in functionality of fungal community in soils, Front. Microbiol., 7, 1897, https://doi.org/10.3389/fmicb.2016.01897, 2016.
Hartmann, A., Schmid, M., van Tuinen, D., and Berg, G.: Plant-driven
selection of microbes, Plant Soil, 321, 235–257, 2009.
Hayat, R., Ali, S., Amara, U., Khalid, R., and Ahmed, I.: Soil beneficial
bacteria and their role in plant growth promotion: A review, Ann.
Microbiol., 60, 579–598, https://doi.org/10.1007/s13213-010-0117-1, 2010.
Haynes, R. J.: Nature of the belowground ecosystem and its development during
pedogenesis, Adv. Agron., 127, 43–109, 2014.
Henry, S., Baudoin, E., Lopez-Gutiérrez, J.-C., Martin-Laurent, F.,
Brauman, A., and Philippot, L.: Quantification of denitrifying bacteria in
soils by nirK gene targeted real-time PCR, J. Microbiol. Meth.,
59, 327–335, 2004.
Herrmann, A. M., Coucheney, E., and Nunan, N.: Isothermal microcalorimetry
provides new insight into terrestrial carbon cycling, Environ. Sci.
Technol., 48, 4344–4352, https://doi.org/10.1021/es403941h, 2014.
Hirsch, P. R., Mauchline, T. H., and Clark, I. M.: Culture-independent
molecular techniques for soil microbial ecology, Soil Biol.
Biochem., 42, 878–887, https://doi.org/10.1016/j.soilbio.2010.02.019, 2010.
ISO 11063: Soil quality – Method to directly extract DNA from soil samples,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/50025.html (last access: 27 January 2020), 2012.
ISO 11266: Soil quality – Guidance on laboratory testing for biodegradation
of organic chemicals in soil under aerobic conditions, International
Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/19244.html (last access: 27 January 2020), 1994.
ISO 14238: Soil quality – Biological methods – Determination of nitrogen
mineralization and nitrification in soils and the influence of chemicals on
these processes, International Organization for Standardization, Geneva,
Switzerland, available at: https://www.iso.org/standard/56033.html (last access: 27 January 2020), 2012.
ISO 14239: Soil quality – Laboratory incubation systems for measuring the
mineralization of organic chemicals in soil under aerobic conditions,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/69583.html (last access: 27 January 2020), 2017.
ISO 14240-1: Soil quality – Determination of soil microbial biomass – Part
1: Substrate-induced respiration method, International Organization for
Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/21530.html (last access: 27 January 2020), 1997.
ISO 14240-2: Soil quality – Determination of soil microbial biomass – Part
2: Fumigation-extraction method, International Organization for
Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/23951.html (last access: 27 January 2020), 1997.
ISO 15473: Soil quality – Guidance on laboratory testing for biodegradation
of organic chemicals in soil under anaerobic conditions, International
Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/27189.html (last access: 27 January 2020), 2002.
ISO 15685: Soil quality – Determination of potential nitrification and
inhibition of nitrification – Rapid test by ammonium oxidation,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/53530.html (last access: 27 January 2020), 2012.
ISO 16072: Soil quality – Laboratory methods for determination of microbial
soil respiration, International Organization for Standardization, Geneva,
Switzerland, available at: https://www.iso.org/standard/32096.html (last access: 27 January 2020), 2002.
ISO 17155: Soil quality – Determination of abundance and activity of soil
microflora using respiration curves, International Organization for
Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/53529.html (last access: 27 January 2020), 2012.
ISO 17601: Soil quality – Estimation of abundance of selected microbial
gene sequences by quantitative PCR from DNA directly extracted from soil,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/60106.html (last access: 27 January 2020), 2016.
ISO 18311: Soil quality – Method for testing effects of soil contaminants
on the feeding activity of soil dwelling organisms – Bait-lamina test,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/62102.html (last access: 27 January 2020), 2016.
ISO 23753-1: Soil quality – Determination of dehydrogenase activity in
soils – Part 1: Method using triphenyltetrazolium chloride (TTC),
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/70145.html (last access: 27 January 2020), 2019.
ISO 23753-2: Soil quality – Determination of dehydrogenase activity in
soils – Part 2: Method using iodotetrazolium chloride (INT), International
Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/70146.html (last access: 27 January 2020), 2019.
ISO 20130: Soil quality – Measurement of enzyme activity patterns in soil
samples using colorimetric substrates in micro-well plates, International
Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/67074.html (last access: 27 January 2020), 2018.
ISO 20951: Soil Quality – Guidance on methods for measuring greenhouse
gases (CO2, N2O, CH4) and ammonia (NH3) fluxes between
soils and the atmosphere, International Organization for Standardization,
Geneva, Switzerland, available at:
https://www.iso.org/standard/69534.html (last access: 27 January 2020), 2018.
ISO/CD 23265: Soil quality – Test for measuring organic matter
decomposition in contaminated soil, International Organization for
Standardization, Geneva, Switzerland, under development,
available at:
https://www.iso.org/standard/75115.html (last access: 27 January 2020), 2018.
ISO/TS 20131-1: Soil quality – Easy laboratory assessments of soil
denitrification, a process source of N2O emissions – Part 1: Soil
denitrifying enzymes activities, International Organization for
Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/67075.html (last access: 27 January 2020), 2018.
ISO/TS 20131-2: Soil quality – Easy laboratory assessments of soil
denitrification, a process source of N2O emissions – Part 2:
Assessment of the capacity of soils to reduce N2O, International
Organization for Standardization, Geneva, Switzerland,
available at: https://www.iso.org/standard/67076.html (last access: 27 January 2020), 2018.
ISO/TS 22939: Soil quality – Measurement of enzyme activity patterns in
soil samples using fluorogenic substrates in micro-well plates,
International Organization for Standardization, Geneva, Switzerland, available at:
https://www.iso.org/standard/41226.html (last access: 27 January 2020), 2019.
ISO/TS 29843-1: Soil quality – Determination of soil microbial diversity –
Part 1: Method by phospholipid fatty acid analysis (PLFA) and phospholipid
ether lipids (PLEL) analysis, International Organization for
Standardization, Geneva, available at: https://www.iso.org/standard/45703.html (last access: 27 January 2020), 2010.
ISO/TS 29843-2: Soil quality – Determination of soil microbial diversity –
Part 2: Method by phospholipid fatty acid analysis (PLFA) using the simple
PLFA extraction method, International Organization for Standardization,
Geneva, available at: https://www.iso.org/standard/54070.html (last access: 27 January 2020), 2011.
Jänsch, S., Scheffczyk, A., and Römbke, J.: The bait lamina test –
A possible screening method for earthworm toxicity testing,
Euro.-Mediterr. J. Environ. Integr., 2, 5, https://doi.org/10.1007/s41207-017-0015-z, 2017.
Janos, D. P., Garamszegi, S., and Beltran, B.: Glomalin extraction and
measurement, Soil Biol. Biochem., 40, 728–739, https://doi.org/10.1016/j.soilbio.2007.10.007, 2008.
Jansson, J. K. and Hofmockel, K. S.: The soil microbiome – from
metagenomics to metaphenomics, Curr. Opin. Microbiol., 43, 162–168,
https://doi.org/10.1016/j.mib.2018.01.013, 2018.
Jeffries, T. C., Rayu, S., Nielsen, U. N., Lai, K., Ijaz, A., Nazaries, L.,
and Singh, B. K.: Metagenomic functional potential predicts degradation rates
of a model organophosphorus xenobiotic in pesticide contaminated soils,
Front. Microbiol., 9, 147, https://doi.org/10.3389/fmicb.2018.00147, 2018.
Jiang, X., Cao, L., Zhang, R., Yan, L., Mao, Y., and Yang, Y.: Effects of nitrogen addition and litter properties on litter decomposition and enzyme activities of individual fungi, Appl. Soil Ecol., 80, 108–115, 2014.
Joergensen, R. G. and Emmerling, C.: Methods for evaluating human impact on
soil microorganisms based on their activity, biomass, and diversity in
agricultural soils, J. Plant Nutr. Soil Sc., 169,
295–309, https://doi.org/10.1002/jpln.200521941, 2006.
Jung, J., Choi, S., Jung, H., Scow, K. M., and Park, W.: Primers for
amplification of nitrous oxide reductase genes associated with Firmicutes
and Bacteroidetes in organic-compound-rich soils, Microbiology, 159,
307–315, https://doi.org/10.1099/mic.0.060194-0, 2013.
Keuskamp, J. A., Dingemans, B. J. J., Lehtinen, L., Sarneel, J. M., and Hefting,
M. M.: Tea Bag Index: a novel approach to collect uniform decomposition data
across ecosystems, Methods Ecol. Evol., 4, 1070–1075, 2013.
Knacker, T., Förster, B., Römbke, J., and Frampton, G. K.: Assessing
the effects of plant protection products on organic matter breakdown in
arable fields – Litter decomposition test systems, Soil Biol.
Biochem., 35, 1269–1287, https://doi.org/10.1016/S0038-0717(03)00219-0, 2003.
Kolb, S., Knief, C., Stubner, S., and Conrad, R.: Quantitative detection of
methanotrophs in soil by novel pmoA-targeted real-time PCR assays, Appl.
Environ. Microb., 69, 2423–2429, https://doi.org/10.1128/AEM.69.5.2423-2429.2003, 2003.
Kuffner, M., Hai, B., Rattei, T., Melodelima, C., Schloter, M.,
Zechmeister-Boltenstern, S., Jandl, R., Schindlbacher, A., and Sessitsch,
A.: Effects of season and experimental warming on the bacterial community in
a temperate mountain forest soil assessed by 16S rRNA gene pyrosequencing,
FEMS Microbiol. Ecol., 82, 551–562, https://doi.org/10.1111/j.1574-6941.2012.01420.x, 2012.
Kvas, S., Rahn, J., Engel, K., Neufeld, J. D., Villeneuve, P. J., Trevors,
J. T., Lee, H., Scroggins, R. P., and Beaudette, L. A.: Development of a
microbial test suite and data integration method for assessing microbial
health of contaminated soil, J. Microbiol. Meth., 143, 66–77,
2017.
Levy-Booth, D. J., Prescott, C. E., and Grayston, S. J.: Microbial
functional genes involved in nitrogen fixation, nitrification and
denitrification in forest ecosystems, Soil Biol. Biochem., 75,
11–25, https://doi.org/10.1016/j.soilbio.2014.03.021, 2014.
Liu, W., Qiao, C., Yang, S., Bai, W., and Liu, L.: Microbial carbon use
efficiency and priming effect regulate soil carbon storage under nitrogen
deposition by slowing soil organic matter decomposition, Geoderma, 332,
37–44, https://doi.org/10.1016/j.geoderma.2018.07.008, 2018.
Lueders, T., Manefield, M., and Friedrich, M. W.: Enhanced sensitivity of
DNA- and rRNA-based stable isotope probing by fractionation and quantitative
analysis of isopycnic centrifugation gradients, Environ. Microbiol.,
6, 73–78, 2004.
Lugtenberg, B. and Kamilova, F.: Plant-growth-promoting rhizobacteria,
Annu. Rev. Microbiol., 63, 541–556, https://doi.org/10.1146/annurev.micro.62.081307.162918, 2009.
Martin-Laurent, F., Cornet, L., Ranjard, L., Lopez-Gutiérrez, J. C.,
Philippot, L., Schwartz, C., Chaussod, R., Catroux, G., and Soulas, G.:
Estimation of atrazine-degrading genetic potential and activity in three
French agricultural soils, FEMS Micobiol. Ecol., 48, 425–435, 2004.
MEA (Millennium Ecosystem Assessment): Ecosystems and Human Well-being:
Synthesis, Island Press, Washington, D.C., 2005.
Modrzyński, J. J., Christensen, J. H., Mayer, P., and Brandt, K. K.:
Limited recovery of soil microbial activity after transient exposure to
gasoline vapors, Environ. Pollut., 216, 826–835, https://doi.org/10.1016/j.envpol.2016.06.054, 2016.
Montgomery, D. R.: Dirt: The Erosion of Civilizations, University of
California Press, Berkeley, Calif., London, 2008.
Nannipieri, P. and Eldor, P.: The chemical and functional characterization
of soil N and its biotic components, Soil Biol. Biochem., 41,
2357–2369, https://doi.org/10.1016/j.soilbio.2009.07.013, 2009.
Nannipieri, P., Greco, S., and Ceccanti, B.: Ecological Significance of the
Biological Activity in Soil, in: Soil Biochemistry, Volume 6,
edited by: Bollag, J. M. and Stotzky, G., Routledge, New York, 293–355,
2017.
Nicol, G. W., Glover, L. A., and Prosser, J. I.: Spatial analysis of
archaeal community structure in grassland soil, Appl. Environ.
Microb., 69, 7420–7429, https://doi.org/10.1128/AEM.69.12.7420-7429.2003, 2003.
Nienstedt, K., Brock, T. C. M., Van Wensem, J., Montforts, M., Hart, A.,
Aagaard, A., Alix, A., Boesten, J., Bopp, S. K., Brown, C., Capri, E.,
Forbes, V., Köpp, H., Liess, M., Luttik, R., Maltby, L., Sousa, J.-P.,
Streissl, F., and Hardy, A. R.: Development of a framework based on an
ecosystem services approach for deriving specific protection goals for
environmental risk assessment of pesticides, Sci. Total
Environ., 415, 31–38, 2012.
Norton, J. M., Alzerreca, J. J., Suwa, Y., and Klotz, M. G.: Diversity of
ammonia monooxygenase operon in autotrophic ammonia-oxidizing bacteria,
Arch. Microbiol., 177, 139–149, https://doi.org/10.1007/s00203-001-0369-z, 2002.
Ockleford, C., Adriaanse, P., Berny, P., Brock, T., Duquesne, S., Grilli,
S., Hernandez-Jerez, A. F., Bennekou, S. H., Klein, M., Kuhl, T., Laskowski,
R., Machera, K., Pelkonen, O., Pieper, S., Stemmer, M., Sundh, I.,
Teodorovic, I., Tiktak, A., Topping, C. J., Wolterink, G., Craig, P., de
Jong, F., Manachini, B., Sousa, P., Swarowsky, K., Auteri, D., Arena, M.,
and Rob, S.: EFSA PPR Panel (EFSA Panel on Plant Protection Products and
their Residues) Scientific Opinion addressing the state of the science on
risk assessment of plant protection products for in-soil organisms, EFSA
Journal, 15, 255, https://doi.org/10.2903/j.efsa.2017.4690, 2017.
OECD: Test No. 216: Soil Microorganisms: Nitrogen Transformation Test,
Paris, France, 2000a.
OECD: Test No. 217: Soil Microorganisms: Carbon Transformation Test, Paris,
France, 2000b.
OECD: OECD Series on Testing and Assessment No. 56, Guidance document on the
breakdown of organic matter in litterbags, ENV/JM/MONO 23, Paris, France,
2006.
Ollivier, J., Kleineidam, K., Reichel, R., Thiele-Bruhn, S., Kotzerke, A.,
Kindler, R., Wilke, B. M., and Schloter, M.: Effect of
sulfadiazine-contaminated pig manure on the abundances of genes and
transcripts involved in nitrogen transformation in the root-rhizosphere
complexes of maize and clover, Appl. Environ. Microb., 76,
7903–7909, 2010.
Ouyang, Y., Reeve, J. R., and Norton, J. M.: Soil enzyme activities and
abundance of microbial functional genes involved in nitrogen transformations
in an organic farming system, Biol. Fert. Soils, 54, 437–450,
2018.
Pankhurst, C. E., Yu, S., Hawke, B. G., and Harch, B. D.: Capacity of fatty
acid profiles and substrate utilization patterns to describe differences in
soil microbial communities associated with increased salinity or alkalinity
at three locations in South Australia, Biol. Fert. Soils, 33,
204–217, 2001.
Parker, S. S.: Buried treasure: Soil biodiversity and conservation,
Biodivers. Conserv., 19, 3743–3756, 2010.
Paul, E. A.: Soil Microbiology, Ecology and Biochemistry, 4th Edn., Academic
Press, Burlington, MA, 2015.
Peng, J., Lü, Z., Rui, J., and Lu, Y.: Dynamics of the methanogenic
archaeal community during plant residue decomposition in an anoxic rice
field soil, Appl. Environ. Microb., 74, 2894–2901, https://doi.org/10.1128/AEM.00070-08, 2008.
Penton, C. R., Gupta, V. V. S. R., Yu, J., and Tiedje, J. M.: Size matters:
Assessing optimum soil sample size for fungal and bacterial community
structure analyses using high throughput sequencing of rRNA gene amplicons,
Front. Microbiol., 7, 824, https://doi.org/10.3389/fmicb.2016.00824, 2016.
Philippot, L., Ritz, K., Pandard, P., Hallin, S., and Martin-Laurent, F.:
Standardisation of methods in soil microbiology: Progress and challenges,
FEMS Microbiol. Ecol., 82, 1–10, https://doi.org/10.1111/j.1574-6941.2012.01436.x,
2012.
Prado, A. G. S. and Airoldi, C.: The effect of the herbicide diuron on soil
microbial activity, Pest Manag. Sci., 57, 640–644 https://doi.org/10.1002/ps.321,
2001.
Prado, A. G. S. and Airoldi, C.: A toxicity view of the pesticide picloram when
immobilized onto a silica gel surface, Anal. Bioanal.
Chem., 376, 686–690, https://doi.org/10.1007/s00216-003-1927-9, 2003.
Preston-Mafham, J., Boddy, L., and Randerson, P. F.: Analysis of microbial
community functional diversity using sole-carbon-source utilisation profiles
– A critique, FEMS Microbiol. Ecol., 42, 1–14, https://doi.org/10.1016/S0168-6496(02)00324-0, 2002.
Pulleman, M., Creamer, R., Hamer, U., Helder, J., Pelose, C., Peres, G., and
Rutgers, M.: Soil biodiversity, biological indicators and soil ecosystem
services – an overview of European approaches, Curr. Opin. Env.
Sust., 4, 529–538, 2012.
Quince, C., Walker, A. W., Simpson, J. T., Loman, N. J., and Segata, N.:
Shotgun metagenomics, from sampling to analysis, Nat. Biotechnol., 35,
833–844, 2017.
Ramirez, K. S., Knight, C. G., De Hollander, M., Brearley, F. Q.,
Constantinides, B., Cotton, A., Creer, S., Crowther, T. W., Davison, J.,
Delgado-Baquerizo, M., Dorrepaal, E., Elliott, D. R., Fox, G., Griffiths,
R. I., Hale, C., Hartman, K., Houlden, A., Jones, D. L., Krab, E. J., Maestre,
F. T., McGuire, K. L., Monteux, S., Orr, C. H., Van Der Putten, W. H., Roberts,
I. S., Robinson, D. A., Rocca, J. D., Rowntree, J., Schlaeppi, K., Shepherd,
M., Singh, B. K., Straathof, A. L., Bhatnagar, J. M., Thion, C., Van Der
Heijden, M. G. A., and De Vries, F. T.: Detecting macroecological patterns in
bacterial communities across independent studies of global soils, Nat.
Microbiol., 3, 189–196, 2018.
Regan, K. M., Nunan, N., Boeddinghaus, R. S., Baumgartner, V., Berner, D.,
Boch, S., Oelmann, Y., Overmann, J., Prati, D., Schloter, M., Schmitt, B.,
Sorkau, E., Steffens, M., Kandeler, E., and Marhan, S.: Seasonal controls on
grassland microbial biogeography: Are they governed by plants, abiotic
properties or both?, Soil Biol. Biochem., 71, 21–30, https://doi.org/10.1016/j.soilbio.2013.12.024, 2014.
Ribbons, R. R., Levy-Booth, D. J., Masse, J., Grayston, S. J., McDonald, M. A.,
Vesterdal, L., and Prescott, C. E.: Linking microbial communities, functional
genes and nitrogen-cycling processes in forest floors under four tree
species, Soil Biol. Biochem., 103, 181–191, https://doi.org/10.1016/j.soilbio.2016.07.024, 2016.
Rillig, M. C.: Arbuscular mycorrhizae, glomalin, and soil aggregation,
Can. J. Soil Sci., 84, 355–363, https://doi.org/10.4141/S04-003, 2004.
Rillig, M. C. and Mummey, D. L.: Mycorrhizas and soil structure, New
Phytol., 171, 41–53, https://doi.org/10.1111/j.1469-8137.2006.01750.x, 2006.
Ritz, K., Black, H. I. J., Campbell, C. D., Harris, J. A., and Wood, C.:
Selecting biological indicators for monitoring soils: A framework for
balancing scientific and technical opinion to assist policy development,
Ecol. Indic., 9, 1212–1221, 2009.
Römbke, J., Jänsch, S., Meier, M., Hilbeck, A., Teichmann, H., and
Tappeser, B.: General recommendations for soil ecotoxicological tests
suitable for the environmental risk assessment (ERA) of genetically modified
plants (GMPs), Integr. Environ. Assess., 6,
287–300, 2010.
Rousk, J.: Biomass or growth? How to measure soil food webs to understand
structure and function, Soil Biol. Biochem., 102, 45–47, https://doi.org/10.1016/j.soilbio.2016.07.001, 2016.
Rousk, J., Demoling, L. A., and Bååth, E.: Contrasting short-term
antibiotic effects on respiration and bacterial growth compromises the
validity of the selective respiratory inhibition technique to distinguish
fungi and bacteria, Microb. Ecol., 58, 75–85, https://doi.org/10.1007/s00248-008-9444-1, 2009a.
Rousk, J., Brookes, P. C., and Bååth, E.: Contrasting soil pH effects
on fungal and bacterial growth suggest functional redundancy in carbon
mineralization, Appl. Environ. Microb., 75, 1589–1596,
https://doi.org/10.1128/AEM.02775-08, 2009b.
Rutgers, M., Wouterse, M., Drost, S. M., Breure, A. M., Mulder, C., Stone,
D., Creamer, R. E., Winding, A., and Bloem, J.: Monitoring soil bacteria
with community-level physiological profiles using Biolog™
ECO-plates in the Netherlands and Europe, Appl. Soil Ecol., 97, 23–35,
https://doi.org/10.1016/j.apsoil.2015.06.007, 2016.
Sakakibara, S. M., Jones, M. D., Gillespie, M., Hagerman, S. M., Forrest, M. E.,
Simard, S. W., and Durall, D. M.: A comparison of ectomycorrhiza
identification based on morphotyping and PCR-RFLP analysis, Mycol.
Res., 106, 868–878, 2002.
Savazzini, F., Longa, C. M., Pertot, I., and Gessler, C. J.: Real-time PCR for
detection and quantification of the biocontrol agent Trichoderma atroviride
strain SC1 in soil, Microbiological Methods, 73, 185–194, https://doi.org/10.1016/j.mimet.2008.02.004, 2008.
Scheu, S., Schlitt, N., Tiunov, A. V., Newington, J. E., and Jones, T. H.:
Effects of the presence and community composition of earthworms on microbial
community functioning, Oecologia, 133, 254–260, https://doi.org/10.1007/s00442-002-1023-4, 2002.
Scheu, S., Ruess, L., and Bonkowski, M.: Interactions between microorganisms
and soil micro- and mesofauna, in: Microorganisms in Soils: Roles in Genesis
and Functions, edited by: Varma, A. and Buscot, F., Vol. 3, Springer, Berlin, Heidelberg,
253–275, 2005.
Schmitt, H., Van Beelen, P., Tolls, J., and Van Leeuwen, C. L.:
Pollution-induced community tolerance of soil microbial communities caused
by the antibiotic sulfachloropyridazine, Environ. Sci.
Technol., 38, 1148–1153, 2004.
Schöler, A., Jacquiod, S., Vestergaard, G., Schulz, S., and Schloter, M.:
Analysis of soil microbial communities based on amplicon sequencing of
marker genes, Biol. Fert. Soils, 53, 485–489, 2017.
Schwartz, E.: Characterization of growing microorganisms in soil by stable
isotope probing with , Appl. Environ.
Microb., 73, 2541–2546, 2007.
Schwartz, E., Hayer, M., Hungate, B. A., Koch, B. J., McHugh, T. A., Mercurio,
W., Morrissey, E. M., and Soldanova, K.: Stable isotope probing with
18O-water to investigate microbial growth and death in environmental
samples, Curr. Opin. Biotech., 41, 14–18, 2016.
Schulz, S., Bergkemper, F., De Vries, M., Schöler, A., and Schloter, M.:
qPCR for quantitative validation of metagenomic data [qPCR zur quantitativen
Validierung von Metagenomdaten], BioSpektrum, 22, 265–269, https://doi.org/10.1007/s12268-016-0684-1, 2016.
Sessitsch, A., Hackl, E., Wenzl, P., Kilian, A., Kostic, T., Stralis-Pavese,
N., Sandjong, B. T., and Bodrossy, L.: Diagnostic microbial microarrays in
soil ecology, New Phytol., 171, 719–736, https://doi.org/10.1111/j.1469-8137.2006.01824.x, 2006.
Singh, B. K., Tate, K. R., Kolipaka, G., Hedley, C. B., Macdonald, C. A.,
Millard, P., and Murrell, J. C.: Effect of afforestation and reforestation
of pastures on the activity and population dynamics of methanotrophic
bacteria, Appl. Environ. Microb., 73, 5153–5161, https://doi.org/10.1128/AEM.00620-07, 2007.
Six, J., Bossuyt, H., Degryze, S., and Denef, K.: A history of research on
the link between (micro)aggregates, soil biota, and soil organic matter
dynamics, Soil Till. Res., 79, 7–31
https://doi.org/10.1016/j.still.2004.03.008, 2004.
Smith, C. J. and Osborn, A. M.: Advantages and limitations of quantitative
PCR (Q-PCR)-based approaches in microbial ecology, FEMS Microbiol.
Ecol., 67, 6–20, https://doi.org/10.1111/j.1574-6941.2008.00629.x, 2009.
Šnajdr, J., Valášková, V., Merhautová, V.,
Herinková, J., Cajthaml, T., and Baldrian, P.: Spatial variability of
enzyme activities and microbial biomass in the upper layers of Quercus
petraea forest soil, Soil Biol. Biochem., 40, 2068–2075, 2008.
Spohn, M., Pötsch, E. M., Eichorst, S. A., Woebken, D., Wanek, W., and
Richter, A.: Soil microbial carbon use efficiency and biomass turnover in a
long-term fertilization experiment in a temperate grassland, Soil Biol. Biochem., 97, 168–175, https://doi.org/10.1016/j.soilbio.2016.03.008, 2016.
Steinberg, L. M. and Regan, J. M.: mcrA-targeted real-time quantitative PCR
method to examine methanogen communities, Appl. Environ.
Microb., 75, 4435–4442, 2009.
Strickland, M. S. and Rousk, J.: Considering fungal: Bacterial dominance in
soils – Methods, controls, and ecosystem implications, Soil Biol.
Biochem., 42, 1385–1395, https://doi.org/10.1016/j.soilbio.2010.05.007, 2010.
Suriyavirun, N., Krichels, A. H., Kent, A. D., and Yang, W. H.:
Microtopographic differences in soil properties and microbial community
composition at the field scale, Soil Biol. Biochem., 131, 71–80,
https://doi.org/10.1016/j.soilbio.2018.12.024, 2019.
Takriti, M., Wild, B., Schnecker, J., Mooshammer, M., Knoltsch, A.,
Lashchinskiy, N., Eloy Alves, R. J., Gentsch, N., Gittel, A., Mikutta, R.,
Wanek, W., and Richter, A.: Soil organic matter quality exerts a stronger
control than stoichiometry on microbial substrate use efficiency along a
latitudinal transect, Soil Biol. Biochem., 121, 212–220, https://doi.org/10.1016/j.soilbio.2018.02.022, 2018.
TEEB: The Economics of Ecosystems and Biodiversity Ecological and Economic
Foundations, edited by: Kumar, P., Earthscan, Routledge, London, UK, 2010.
Thiele-Bruhn, S., Bloem, J., de Vries, F. T., Kalbitz, K., and Wagg, C.:
Linking soil biodiversity and agricultural soil management, Curr. Opin.
Env. Sust., 4, 523–528, 2012.
Tian, J., He, N., Hale, L., Niu, S., Yu, G., Liu, Y., Blagodatskaya, E.,
Kuzyakov, Y., Gao, Q., and Zhou, J.: Soil organic matter availability and
climate drive latitudinal patterns in bacterial diversity from tropical to
cold temperate forests, Funct. Ecol., 32, 61–70, https://doi.org/10.1111/1365-2435.12952, 2018.
Traugott, M., Kamenova, S., Ruess, L., Seeber, J., and Plantegenest, M.:
Empirically characterising trophic networks: What emerging DNA-based
methods, stable isotope and fatty acid analyses can offer, Adv.
Ecol. Res., 49, 177–224, 2013.
Van der Putten, W. H., Mudgal, S., Turbé, A., Toni, A. D., Lavelle, P.,
Benito, P., and Ruiz, N.: Soil biodiversity: functions, threats and tools
for policy makers, Bio Intelligence Service, Paris, France, 2010.
Voříšková, A., Jansa, J., Püschel, D., Krüger, M.,
Cajthaml, T., Vosátka, M., and Janoušková, M.: Real-time PCR
quantification of arbuscular mycorrhizal fungi: does the use of nuclear or
mitochondrial markers make a difference?, Mycorrhiza, 27, 577–585, https://doi.org/10.1007/s00572-017-0777-9, 2017.
Wagg, C., Bender, S. F., Widmer, F., and Van Der Heijden, M. G. A.: Soil
biodiversity and soil community composition determine ecosystem
multifunctionality, P. Natl. Acad. Sci. USA, 111, 5266–5270, https://doi.org/10.1073/pnas.1320054111, 2014.
Wallenstein, M. D., Myrold, D. D., Firestone, M., and Voytek, M.:
Environmental controls on denitrifying communities and denitrification
rates: Insights from molecular methods, Ecol. Appl., 16,
2143–2152, https://doi.org/10.1890/1051-0761(2006)016[2143:ECODCA]2.0.CO;2, 2006.
Wardle, D. A. and Ghani, A.: A critique of the microbial metabolic quotient
(qCO2) as a bioindicator of disturbance and ecosystem development, Soil
Biol. Biochem., 27, 1601–1610, https://doi.org/10.1016/0038-0717(95)00093-T,
1995.
Winding, A. and Hendriksen, N. B.: Comparison of CLPP and enzyme activity
assay for functional characterization of bacterial soil communities, J. Soil. Sediment., 7, 411–417, https://doi.org/10.1065/jss2007.11.262, 2007.
Wright, S. F., Upadhyaya, A., and Buyer, J. S.: Comparison of N-linked
oligosaccharides of glomalin from arbuscular mycorrhizal fungi and soils by
capillary electrophoresis, Soil Biol. Biochem., 30, 1853–1857, https://doi.org/10.1016/S0038-0717(98)00047-9, 1998.
Xia, W., Zhang, C., Zeng, X., Feng, Y., Weng, J., Lin, X., Zhu, J., Xiong,
Z., Xu, J., Cai, Z., and Jia, Z.: Autotrophic growth of nitrifying community
in an agricultural soil, ISME J., 5, 1226–1236, https://doi.org/10.1038/ismej.2011.5, 2011.
Xu, S., Feng, S., Sun, H., Wu, S., Zhuang, G., Deng, Y., Bai, Z., Jing, C.,
and Zhuang, X.: Linking N2O emissions from biofertilizer-amended soil
of tea plantations to the abundance and structure of N2O-reducing
microbial communities, Environ. Sci. Technol., 52,
11338–11345, https://doi.org/10.1021/acs.est.8b04935, 2018.
Xue, K., Zhou, J., Van Nostrand, J., Mench, M., Bes, C., Giagnoni, L., and
Renella, G.: Functional activity and functional gene diversity of a
Cu-contaminated soil remediated by aided phytostabilization using compost,
dolomitic limestone and a mixed tree stand, Environ. Pollut., 242,
229–238, 2018.
Yates, M. V., Nakatsu, C. H., Miller, R. V., and Pillai, S. D.: Manual of
Environmental Microbiology, 4th Edn., American Society of
Microbiology, Washington DC, USA, 2016.
Yergeau, E., Hogues, H., Whyte, L. G., and Greer, C. W.: The functional
potential of high Arctic permafrost revealed by metagenomic sequencing, qPCR
and microarray analyses, ISME J., 4, 1206–1214, https://doi.org/10.1038/ismej.2010.41, 2010.
Zhang, K., Li, X., Cheng, X., Zhang, Z., and Zhang, Q.: Changes in soil
properties rather than functional gene abundance control carbon and nitrogen
mineralization rates during long-term natural revegetation, Plant Soil,
443, 293–306, 2019.
Short summary
Soil quality depends on the functioning of soil microbiota. Only a few standardized methods are available to assess this as well as adverse effects of human activities. So we need to identify promising additional methods that target soil microbial function. Discussed are (i) molecular methods using qPCR for new endpoints, e.g. in N and P cycling and greenhouse gas emissions, (ii) techniques for fungal enzyme activities, and (iii) field methods on carbon turnover such as the litter bag test.
Soil quality depends on the functioning of soil microbiota. Only a few standardized methods are...