The DOI matches its Crossref record; 113 of the 113 references it cites were found in a registry or an index.
Rhizosphere size and shape: Temporal dynamics and spatial stationarity
Abstract
Abstract The soil volume affected by roots – the rhizosphere – is one of the most important microbial hotspots determining the processes, dynamics and cycling of carbon (C), nutrients and water in terrestrial ecosystems. Rhizosphere visualization is necessary to understand, localize and quantify the ongoing processes and functions, but quantitative conclusions are very uncertain because of: 1) the continuum of the parameters between the root surface and root-free soil, i.e., there are no sharp borders, 2) differences in the distributions of various parameters (C, nutrients, pH, enzyme and microbial activities, gases, water etc.) across and along roots, 3) temporal changes of the parameters and processes with root growth as well as with water and C flows. In situ techniques: planar optodes, zymography, sensitive gels, 14C and neutron imaging as well as destructive approaches (thin layer slicing) have been used to analyze the rhizosphere extent and the gradients of various physico-chemical and biological characteristics: pH, CO2, O2, redox potential, enzyme activities, content of water, nutrients and excess elements, and organic compounds. A literature analysis allows the conclusion that: i) the rhizosphere extent for most of the parameters assessed by non-destructive visualization techniques is 0.5–4 mm but exceeds 4 mm for gases, nitrate, water and redox potential. ii) The rhizosphere extent of nutrients (N, P) is decoupled from the extent of the corresponding enzyme activities. iii) The imbalance between element flows to and uptake by roots may lead to accumulation of excess elements and formation of root carapaces (e.g. CaCO3 rhizoliths, Fe plaque) ranging up to a few cm. iv) All destructive approaches show a much (3–5 times) larger rhizosphere extent compared to visualization techniques. These conclusions are crucial for a mechanistic understanding of rhizosphere properties and functioning, estimation of the nutrient stocks available to roots, and for rhizosphere modelling considering root growth and architecture. Overall, roots function as ecosystem engineers and build their environment, serving as the main factors shaping rhizosphere extent. Sharp gradients are formed within a few days for nutrients and enzymes, but more time is necessary for the establishment of specific microbial communities. Despite the very strong dynamics of most parameters, their stationarity is reached within a few days because the release of C and enzymes or nutrient uptake are very quickly compensated by utilization by surrounding microorganisms or/and sorption and diffusion processes. We conclude that despite the dynamic nature of each property, the rhizosphere gradients, their extent and shape are quasi-stationary because of the opposite directions of their formation processes.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Proceedings of the National Academy of Sciences, USA
(1996) · Current Biology · doi:10.1016/s0960-9822(09)00431-x · Cited by 5,258
THE ROLE OF ROOT EXUDATES IN RHIZOSPHERE INTERACTIONS WITH PLANTS AND OTHER ORGANISMS
Bais, H. P., Weir, T. L., Perry, L. G., Gilroy, S., & Vivanco, J. M. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105159 · Cited by 4,682
Microbial hotspots and hot moments in soil: Concept & review
Kuzyakov, Y., & Blagodatskaya, E. (2015) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2015.01.025 · Cited by 1,872
Self-citationCarbon flow in the rhizosphere: carbon trading at the soil–root interface
Jones, D. L., Nguyen, C., & Finlay, R. D. (2009) · Plant and Soil · doi:10.1007/s11104-009-9925-0 · Cited by 1,710
Hinsinger, P., Plassard, C., Tang, C., & Jaillard, B. (2003) · Plant and Soil · doi:10.1023/a:1022371130939 · Cited by 1,402
Plant and mycorrhizal regulation of rhizodeposition
Jones, D. L., Hodge, A., & Kuzyakov, Y. (2004) · New Phytologist · doi:10.1111/j.1469-8137.2004.01130.x · Cited by 1,371
Self-citationRhizosphere: biophysics, biogeochemistry and ecological relevance
Hinsinger, P., Bengough, A. G., Vetterlein, D., & Young, I. M. (2009) · Plant and Soil · doi:10.1007/s11104-008-9885-9 · Cited by 1,270
Building roots in a changing environment: implications for root longevity
EISSENSTAT, D. M., WELLS, C. E., YANAI, R. D., & WHITBECK, J. L. (2000) · New Phytologist · doi:10.1046/j.1469-8137.2000.00686.x · Cited by 1,092
Plant-driven selection of microbes
Hartmann, A., Schmid, M., Tuinen, D. V., & Berg, G. (2009) · Plant and Soil · doi:10.1007/s11104-008-9814-y · Cited by 1,088
Dennis, P. G., Miller, A. J., & Hirsch, P. R. (2010) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2010.00860.x · Cited by 1,038
Cited by
Pugnaire, F. I., Morillo, J. A., Peñuelas, J., Reich, P. B., Bardgett, R. D., Gaxiola, A., Wardle, D. A., & van der Putten, W. H. (2019) · Science Advances · doi:10.1126/sciadv.aaz1834 · Cited by 513
Caporale, A. G., Amato, M., Duri, L. G., Bochicchio, R., De Pascale, S., Simeone, G. D. R., Palladino, M., Pannico, A., Rao, M. A., Rouphael, Y., et al. (2022) · Plants · doi:10.3390/plants11233345 · Cited by 36
Giannetta, B., Caporale, A. G., Olivera de Souza, D., Adamo, P., & Zaccone, C. (2025) · Environmental Research · doi:10.1016/j.envres.2025.122362 · Cited by 4
Metadata
- Authors
- Kuzyakov, Y., & Razavi, B. S.
- Venue
- Soil Biology and Biochemistry
- Publisher
- Elsevier BV
- Published
- 2019-08
- Volume
- 135
- Pages
- 343-360
- ISSN
- 0038-0717 (ISSN-L)
- OpenAlex
- W2945642553
- Cited by
- 759
- References
- 113
- FWCI
- 47.38
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Rhizosphere size and shape: Temporal dynamics and spatial stationarity. https://app.cochat.ai/papers/10.1016/j.soilbio.2019.05.011
- The paper
- Kuzyakov, Y., & Razavi, B. S. (2019). Rhizosphere size and shape: Temporal dynamics and spatial stationarity. Soil Biology and Biochemistry. https://doi.org/10.1016/j.soilbio.2019.05.011
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.