The DOI matches its Crossref record; 218 of the 218 references it cites were found in a registry or an index.
Arbuscular mycorrhizal fungi in alleviation of salt stress: a review
Open accessAbstract
BACKGROUND: Salt stress has become a major threat to plant growth and productivity. Arbuscular mycorrhizal fungi colonize plant root systems and modulate plant growth in various ways. SCOPE: This review addresses the significance of arbuscular mycorrhiza in alleviation of salt stress and their beneficial effects on plant growth and productivity. It also focuses on recent progress in unravelling biochemical, physiological and molecular mechanisms in mycorrhizal plants to alleviate salt stress. CONCLUSIONS: The role of arbuscular mycorrhizal fungi in alleviating salt stress is well documented. This paper reviews the mechanisms arbuscular mycorrhizal fungi employ to enhance the salt tolerance of host plants such as enhanced nutrient acquisition (P, N, Mg and Ca), maintenance of the K(+) : Na(+) ratio, biochemical changes (accumulation of proline, betaines, polyamines, carbohydrates and antioxidants), physiological changes (photosynthetic efficiency, relative permeability, water status, abscissic acid accumulation, nodulation and nitrogen fixation), molecular changes (the expression of genes: PIP, Na(+)/H(+) antiporters, Lsnced, Lslea and LsP5CS) and ultra-structural changes. Theis review identifies certain lesser explored areas such as molecular and ultra-structural changes where further research is needed for better understanding of symbiosis with reference to salt stress for optimum usage of this technology in the field on a large scale. This review paper gives useful benchmark information for the development and prioritization of future research programmes.
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Microorganisms, and especially mycorrhiza, also play crucial roles in plant resistance to drought and osmotic stress and the tolerance against episodes of freezing and thawing.”
From Intensify production, transform biomass to energy and novel goods and protect soils in Europe—A vision how to mobilize marginal lands (2018) · cites this paper as Evelin et al., 2009
In the citing paper
“Established mechanisms include the mycelium, which has a smaller diameter than root hairs and therefore better access to bound water (Lehto and Zwiazek, 2011) and various mechanisms protecting the mycorrhizal fungus (and therefore also the plant root) from osmotic stress, such as accumulation of osmolytes (mannitol, trehalose); surface hydrophobicity and bacterial secretion of exopolysaccharides (”
From Intensify production, transform biomass to energy and novel goods and protect soils in Europe—A vision how to mobilize marginal lands (2018) · cites this paper as Evelin et al., 2009
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
Items 201–218 of 218
Chlorophyll fluorescence, stress and survival in populations of Mediterranean grassland species
Figueroa, M. E., Fernández‐Baco, L., Luque, T., et al. (1997) · Journal of Vegetation Science · doi:10.2307/3237033 · Cited by 40
Bacteroids Are Stable during Dark-Induced Senescence of Soybean Root Nodules
Sarath, G., Pfeiffer, N. E., Sodhi, C. S., et al. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.82.2.346 · Cited by 40
Mancuso, S., & Rinaldelli, E. (1996) · Advances in Horticultural Science · doi:10.1400/75445 · Cited by 39
Vesicular-Arbuscular Mycorrhizae of Halophytic Grasses in the Alvord Desert of Oregon
Ho, I. (1987) · Research Exchange (Washington State University) · Cited by 38
Histochemical characteristics of Glomus etunicatus infection of Citrus limon fibrous roots
Nemec, S. J. (1981) · Canadian Journal of Botany · doi:10.1139/b81-086 · Cited by 38
Saint-Etienne, L., Paul, S., Imbert, D., et al. (2006) · Forest Ecology and Management · doi:10.1016/j.foreco.2006.05.046 · Cited by 35
INCREASED UPTAKE OF BROMIDE AND CHLORIDE BY PLANTS INFECTED WITH VESICULAR‐ARBUSCULAR MYCORRHIZAS
Buwalda, J. G., Stribley, D. P., & Tinker, P. B. (1983) · New Phytologist · doi:10.1111/j.1469-8137.1983.tb03426.x · Cited by 35
Yamane, K., Rahman, S., Kawasaki, M., et al. (2004) · Plant Production Science · doi:10.1626/pps.7.435 · Cited by 30
Azcón, R., & Barea, J. M. (1992) · Biology and Fertility of Soils · doi:10.1007/bf00336272 · Cited by 29
Betaine status in wheat in relation to nitrogen stress and to transient salinity stress
Grattan, S. R., & Grieve, C. M. (1985) · Plant and Soil · doi:10.1007/bf02197795 · Cited by 29
Soil salinity and arbuscular mycorrhizal colonization of Puccinellia nuttalliana
Johnson-Green, P., Kenkel, N. C., & Booth, T. (2001) · Mycological Research · doi:10.1017/s095375620100452x · Cited by 27
Baker, A., Sprent, J. I., & Wilson, J. K. (1995) · DalSpace (Dalhousie University) · Cited by 24
Muok, B. O., & Ishii, T. (2006) · Journal of the Japanese Society for Horticultural Science · doi:10.2503/jjshs.75.26 · Cited by 23
Fuel and forage production from salt affected wasteland in India.
Abrol, I. P. (1986) · Cited by 19
Biochemical changes in Ziziphus xylopyrus by VA mycorrhizae
Mathur, N., & Vyas, A. (1996) · Cited by 18
Adaptive Components of Salt Tolerance
O’Leary, J. W. (2001) · CRC Press eBooks · doi:10.1201/9780203908426.ch30 · Cited by 15
Growth and Physiological Adaptations of Grasses to Salinity Stress
Marcum, K. B. (2001) · CRC Press eBooks · doi:10.1201/9780203908426-34 · Cited by 15
Mahmoodzad, H. (2008) · Pakistan Journal of Biological Sciences · doi:10.3923/pjbs.2008.1161.1164 · Cited by 10
Research works printed but not linked: 9
- Bhaskaran, 1997, Seasonal incidence and distribution of VAM fungi in native saline soils, Journal of Environmental Biology, 18, 209
- Brundrett, 1991, Mycorrhizas in natural ecosystem, Advances in Ecological Research, 21, 300
- El-Desouky, 1998, Growth perfomance of citrus rootstocks under saline conditions, Alexandria Journal of Agricultural Research, 43, 231
- Harisnaut, 2003, Salinity effects on antioxidant enzymes in mulberry cultivar, Science Asia, 29, 109, 10.2306/scienceasia1513-1874.2003.29.109 · DOI
- Lindermann, 1994, Role of VAM in biocontrol, 1
- Smith, 1995, Mycorrhizal symbiosis, 105
- Thanna, 1994, Salinity and mycorrhizal association in relation to carbohydrate status, leaf chlorophyll and activity of peroxidase and polyphenol oxidase enzymes in sour orange seedlings, Alexandria Journal of Agricultural Research, 39, 263
- Tinker, 1975, Soil chemistry of phosphorus and mycorrhizal effects on plant growth, 353
- Xu, 2000, Advances in chloride nutrition, Advances in Agronomy, 68, 96
Cited by
Sorted by citations
Schröder, P., Beckers, B., Daniels, S., Gnädinger, F., Maestri, E., Marmiroli, N., Mench, M., Millan, R., Obermeier, M. M., Oustriere, N., et al. (2018) · Science of The Total Environment · doi:10.1016/j.scitotenv.2017.10.209 · Cited by 151
Metadata
- Authors
- Evelin, H., Kapoor, R., & Giri, B.
- Affiliations
- University of Delhi (IN)
- Venue
- Annals of Botany
- Publisher
- Oxford University Press (OUP)
- Published
- 2009-10-08
- Volume
- 104
- Issue
- 7
- Pages
- 1263-1280
- ISSN
- 0305-7364 (ISSN-L)
- 1095-8290
- PMC
- PMC2778396
- OpenAlex
- W2131136324
- Cited by
- 1,083
- References
- 218
- Citations by year
- 2026: 43 · 2025: 52 · 2024: 67 · 2023: 70 · 2022: 74 · 2021: 94 · 2020: 102 · 2019: 94 · 2018: 73 · 2017: 89 · 2016: 61 · 2015: 51 · 2014: 65 · 2013: 60 · 2012: 40
- FWCI
- 2.47
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annals of Botany (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Council of Scientific and Industrial Research, India
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Mycorrhizal Fungi and Plant Interactions
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Stress Responses and Tolerance
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
- Keywords
- arbuscular mycorrhizal fungi, salt stress, salt tolerance, plant-microbe symbiosis, nutrient acquisition, Na+/K+ ratio, proline accumulation, betaine, polyamines, antioxidants, photosynthetic efficiency, water status, abscisic acid, nodulation, nitrogen fixation, PIP aquaporins, Na+/H+ antiporter, gene expression
- MeSH terms
- Sodium Chloride, Soil Microbiology, Stress, Physiological, Sodium-Hydrogen Exchangers, Magnoliopsida, Mycorrhizae, Salinity
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