- Ecology and evolution of symbiotic fungi
- Fungal influence on soil biogeochemical processes
Under natural conditions the health and survival of plants depend on their symbiotic fungal partners. Molecular identification methods has revolutionized soil microbial ecology and unraveled a tremendous fungal diversity in soil that we are only beginning to truly appreciate. However, general ecological principles governing high fungal diversity remain largely unknown and community composition itself tells us very little about the functioning of soil ecosystems. The long-term goal of our research is to overcome these problems by addressing distribution of adaptive traits in communities along natural substrate gradients; study the phylogenetic rank of niche specificity in soil fungi and exploring the nature of adaptation to heterogeneous soil environments.
We explore the link between ecosystem functions and fungal biodiversity by combining molecular ecology tools with traditional culture based methods. This approach has allowed us to describe the ubiquitous ancient fungal class Archaeorhizomycetes, a.k.a. Soil Clone Group 1, (Science 333, 876-879). These fungi are diverse and occur in roots and soil from most terrestrial ecosystems but their ecological role and means of dispersal remains a mystery. In our research we continue to explore function, distribution and diversity of the class and argue that it remain under-represented in environmental studies due to frequent use of primers with known biases against the class, i.e. the reversed primers ITS4 (Schadt and Rosling, 2014). As highlighted in Tedersoos response to our comment the abundance of the class is very difficult to estimate due to amplification and sequencing biases favoring its short reads over that of other members of fungal communities.
Ylva Strid will conduct her Post doctoral training in our group in collaboration with Prof Diana Six at University of Montana. Her research will address how bark beetle strategies and fungal associates affect breeding success of the beetle. Surprisingly, after more than a century of bark beetle research no one has addressed whether fungi associated with non-mycangial beetles actually affect beetle success. This work is ground-breaking in its focus on the effects of fungi on non-mycangial beetles as well as the use of molecular techniques to describe the fungi associated with both mycangial and non-mycangial beetles. It is also the first to document fungal associations with major non-mycangial beetles throughout their development and their potential to benefit beetles through nitrogen (N) concentration.
With funding from ERC we are developing a new research program on arbuscular mycorrhizal (AM) fungi. AM fungi form symbiotic interactions with almost all terrestrial plants and have done so since plants first colonized land. We are interested in their evolutionary stability and genome organization. Shadi Saraei and Merce Montoliu who has joined us as PhD students in this program. The project aims at characterizing the structure of genetic variability within AM fungal species and is a collaboration with Prof James Bever at the University of Kansas.
During the spring and early summer of 2016 we have started sampling and isolations efforts at the Kungsängen Nature reserve in Uppsala.
Schadt CW, Rosling A (2015) Comment on “Global diversity and geography of soil fungi”. Science 348, 1438.
Menkis A, Urbina H, James TY, Rosling A (2014) Archaeorhizomyces borealis sp. nov. and a sequence-based classification of related soil fungal species. Fungal Biology 118, 943-955
Strid Y., Schroeder M., Lindahl B., Ihrmark K. & Stenlid J. (2014). Bark beetle has a decisive impact on fungal community in Norway spruce stem sections Fungal Ecology, 47-58.
Rosling A, Cox F, Cruz-Martinez K, Ihrmark K, Grelet G-A, Lindahl BD, Menkis A, James TY (2011) Archaeorhizomycetes: unearthing an ancient class of ubiquitous soil fungi. Science, 333: 876-879.
Soils develop as a result of their biological processes while constrained by the environmental and geochemical conditions of a site. Soils in turn provide the environmental constrains that soil fungi adapt to in order to, form associations with host, compete for substrate and to complete their life cycle. Fungi are well adapted to the temporally and spatially heterogeneous soil environment. Thin hyphae allow for efficient substrate exploration and provide large surface area for uptake. Resource translocation within the mycelia allows fungi to link spatially separated substrates, i.e. the carbon supply in its host roots with sources for nutrient uptake in soil. Research in the group addresses the interaction between soil microbial communities and soil process at different spatial and temporal scales. Together with Prof Marianne Clarholm and Ulf Skylberg we have proposed a model for how chelating agents and enzymes act together to release nutrient from less available forms of organic material in soil. This un-button model challenges the way we think about nutrient availability in soil.
Soil microbial communities influence soil processes and hence soil development. As an essential nutrient, phosphorus has intrinsically low availability in soil and root associated fungi are central in its acquisition to plants. The soil microbial biomass itself may however be an even more important driver for phosphorus mobilization and its transformation between organic and inorganic forms. Not only are their biomass a large sink for nutrient uptake but also their necromass provide a huge source of nutrients for future generations. In an collaboration with Rich Phillips at Indiana University, Bloomington we study the role of contrasting types mycorrhizal association (AM vs. ECM) on phosphors cycling in deciduous forests soils. We found that in deciduous forests the type of mycorrhizal association determines the P cycling with recalcitrant organic P accumulating in stands dominated by AM fungi while organic P availability was higher in ECM stands. In the fall Anna Rosling is invited to present these results and discuss the role of symbiotic fungi in P cycling at the Organic P workshop in England (https://op2016.com).
During 2015 Veera Kainiemi visited our group as part of a collaborative project with Dr Anke Herrmann and Dr Petra Fransson, both at SLU. The project explored the thermodynamics of soils collected across a stand age gradient in Uppland to identify a functional link between compositions of soil fungal communities and their ability to utilize carbon substrates of different complexity.
Energy is continuously transformed in soil systems through the metabolic activities of living organisms. Heterotrophic microorganisms utilize energy stored in organic matter and exchange it within the biosphere and with the atmosphere. Thus, different soil microbial communities are likely to call upon different biochemical pathways resulting in different carbon and energy flows through the communities and ecosystems. However, little is known about the energy flows and how they are linked to the carbon cycle and if there is a relation between microbial energetics and microbial community composition in the soil. In this project we study microbial energetics, activity and community structure in boreal forest soils at different succession stages. Working hypotheses are that in higher succession stages microbial diversity increases; the community becomes more energy efficient and specialized to use greater variety of carbon compounds as their energy source. We use isothermal microcalorimetry and multiple substrate-induced soil respiration to quantify energy flows and microbial activity and molecular ecology tools to study the fungal diversity and community structure.
Rosling A, Midgley MG, Cheeke T, Urbina H, Fransson P, Phillips RP (2016) Phosphorus cycling in deciduous forest soil differs between stands dominated by ecto- and arbuscular mycorrhizal trees. New Phytologist 209, 1184-1195.
Clarholm M, Skyllberg U, Rosling A (2015) Organic acid induced release of nutrients from metal-stabilized soil organic matter – The unbutton model. Soil Biology and Biochemistry 84, 168-176.
Rosling A (2009) Trees, mycorrhiza and minerals - field relevance of in vitro experiment. Geomicrobiology Journal. 26: 389-401.
Rosling A, Roose T, Herrmann AM, Davidson FA, Finlay RD, Gadd GM (2009) Approaches to modelling mineral weathering by fungi. Fungal Biology Reviews, 23: 138-144.
Rosling A, Suttle KB, Johansson E, van Hees PAW & Banfield JF (2007) Phosphorus availability affects soil fungal dissolution of apatite. Geobiology, 5: 265-280.