I estimated atmospheric input of C (photosynthesis) and N (N2 fixation) in three common tundra moss species through one growing season under experimental climate warming and evaluated possible effects this could gave on the ecosystem. N2 fixation and photosynthesis were collected 5 times during the growing season at eight field sites above the alpine treeline. I also assessed moss growth, nitrogen and phosphorous leaching and C and N in moss tissue content (as a measure of decomposability). The main finding of these results are that moss water content determines the magnitude of the warming response. With some deviations, mosses that hold on to moisture well, mosses in wet habitats and mosses during wet season increased their, N2 fixation, growth or photosynthesis under warming. This has implications for our predictions of climate change effects on the C and N cycle and shows that moisture is a key factor in regulating warming responses. These results are under preparation for publishing
As nitrogen is highly limiting for growth in cold ecosystems, it is possible that other organisms, eg. plants and fungi, will try to get hold of nitrogen entering the ecosystem via mosses. To describe fungal community composition in the moss layer, I collected moss shoots from 2 experiments in Sweden. One in Boreal and one in subarctic forest. I analysed shoots for 15N and 13C content and for fungal community composition and total fungal biomass. Fungal community analysis revealed that plant-associated fungi are present all the way up into the living moss tissue. These results are currently being remade with some methodological adjustments. The planned manuscript is therefore still under preparation.
To directly trace nitrogen from the moss into the rest of the ecosystem, I used labeled N (15N) added to the moss. I created 144 controlled mini-ecosystems containing soil, one of two plant species and moss covering the soil. Soil and plants were separated from the moss with one of 3 meshes of varying sizes. In this way, 15N in mosses could enter the soil-plant compartment 1) only through free water transport, 2) through both water transport and mycorrhizal colonisation of the moss or 3) through any mechanism also including plant roots growing into the moss layer. Plants established well but did not grow as fast as anticipated. I therefore decided to postpone the planned harvest of pots in 2019 to 2020. Instead, in 2019 preliminary samples of plant leaves were taken and analysed for 15N. These showed that we could trace 15N which confirms that the concentrations added are sufficient for our purpose. However, after only one year we did not see any difference in plant 15N concentration between plant with different access to moss N. This year I and MSc will finalise the project. She will include the results in her MSc thesis and I will synthesise the result in a manuscript for publication.