Resilience to multiple stressors in an aquatic plant and its microbiome
- PMID:31879950
- DOI: 10.1002/ajb2.1404
Resilience to multiple stressors in an aquatic plant and its microbiome
Abstract
Premise: Outcomes of species interactions, especially mutualisms, are notoriously dependent on environmental context, and environments are changing rapidly. Studies have investigated how mutualisms respond to or ameliorate anthropogenic environmental changes, but most have focused on nutrient pollution or climate change and tested stressors one at a time. Relatively little is known about how mutualisms may be altered by or buffer the effects of multiple chemical contaminants, which differ fundamentally from nutrient or climate stressors and are especially widespread in aquatic habitats.
Methods: We investigated the impacts of two contaminants on interactions between the duckweed Lemna minor and its microbiome. Sodium chloride (salt) and benzotriazole (a corrosion inhibitor) often co-occur in runoff to water bodies where duckweeds reside. We tested three L. minor genotypes with and without the culturable portion of their microbiome across field-realistic gradients of salt (3 levels) and benzotriazole (4 levels) in a fully factorial experiment (24 treatments, tested on each genotype) and measured plant and microbial growth.
Results: Stressors had conditional effects. Salt decreased both plant and microbial growth and decreased plant survival more as benzotriazole concentrations increased. In contrast, benzotriazole did not affect microbial abundance and even benefited plants when salt and microbes were absent, perhaps due to biotransformation into growth-promoting compounds. Microbes did not ameliorate duckweed stressors; microbial inoculation increased plant growth, but not at high salt concentrations.
Conclusions: Our results suggest that multiple stressors matter when predicting responses of mutualisms to global change and that beneficial microbes may not always buffer hosts against stress.
Keywords: Lemna minor; Lemnaceae; benzotriazole; biotransformation; duckweed; freshwater salinization; rhizosphere; species interactions; stress; urban pollution.
© 2019 Botanical Society of America.
References
LITERATURE CITED
- Adamsen, F., P. J. Pinter, E. M. Barnes, R. L. LaMorte, G. W. Wall, S. W. Leavitt, and B. A. Kimball. 1999. Measuring wheat senescence with a digital camera. Crop Science 39: 719-724.
- Alvey, J. K., B. Hagedorn, and A. Dotson. 2016. Benzotriazole enrichment in snowmelt discharge emanating from engineered snow storage facilities. Water Environment Research 88: 510-520.
- Ashander, J., L.-M. Chevin, and M. L. Baskett. 2016. Predicting evolutionary rescue via evolving plasticity in stochastic environments. Proceedings of the Royal Society, B, Biological Sciences 283: 20161690.
- Bal, H. B., L. Nayak, S. Das, and T. K. Adhya. 2013. Isolation of ACC deaminase producing PGPR from rice rhizosphere and evaluating their plant growth promoting activity under salt stress. Plant and Soil 366: 93-105.
- Bolyen, E., J. R. Rideout, M. R. Dillon, N. A. Bokulich, C. Abnet, G. A. Al-Ghalith, H. Alexander, et al. 2019. QIIME 2: Reproducible, interactive, scalable, and extensible microbiome data science. Nature Biotechnology 37: 852-857.
Publication types
MeSH terms
Substances
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
