Most manipulation experiments simulating global change in tundra were short-term or did not measure plant growth directly. Here, we assessed the growth of three shrubs (Cassiope tetragona, Empetrum ...hermaphroditum and Betula nana) at a subarctic heath in Abisko (Northern Sweden) after 22 years of warming (passive greenhouses), fertilisation (nutrients addition) and shading (hessian fabric), and compare this to observations from the first decade of treatment. We assessed the growth rate of current-year leaves and apical stem (primary growth) and cambial growth (secondary growth), and integrated growth rates with morphological measurements and species coverage. Primary- and total growth of Cassiope and Empetrum were unaffected by manipulations, whereas growth was substantially reduced under fertilisation and shading (but not warming) for Betula. Overall, shrub height and length tended to increase under fertilisation and warming, whereas branching increased mostly in shaded Cassiope. Morphological changes were coupled to increased secondary growth under fertilisation. The species coverage showed a remarkable increase in graminoids in fertilised plots. Shrub response to fertilisation was positive in the short-term but changed over time, likely because of an increased competition with graminoids. More erected postures and large, canopies (requiring enhanced secondary growth for stem reinforcement) likely compensated for the increased light competition in Empetrum and Cassiope but did not avoid growth reduction in the shade intolerant Betula. The impact of warming and shading on shrub growth was more conservative. The lack of growth enhancement under warming suggests the absence of long-term acclimation for processes limiting biomass production. The lack of negative effects of shading on Cassiope was linked to morphological changes increasing the photosynthetic surface. Overall, tundra shrubs showed developmental plasticity over the longer term. However, such plasticity was associated clearly with growth rate trends only in fertilised plots.
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DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
Freeze–thaw fluctuations in soil temperature may be critical events in the annual pattern of nutrient mobilisation that supplies plant growth requirements in some temperate, and most high latitude ...and high altitude ecosystems. We investigated the effects of two differing freeze–thaw regimes, each of which is realistic of in situ spatial and temporal variation in field conditions, on C and N dynamics in sub-arctic heath tundra mesocosms. In addition,
15N isotopic label was used to follow the partitioning of a labile N pool between major ecosystem components, both during the freeze–thaw treatments phase, and in a subsequent equilibration phase. A single deep freeze treatment phase enhanced dissolved total and labelled N pools in the soil solution at initial thaw, and resulted in reduced pool sizes at the end of the equilibration phase. By contrast, a multiple freeze–thaw cycling treatment directly enhanced the dissolved labelled N pool, but did not significantly affect dissolved total N. Furthermore, both dissolved labelled N and dissolved total N pools were significantly enhanced in the equilibration period following multiple freeze–thaw, the latter due to a marked increase in soil solution NH
4
+. Microbial biomass C was not significantly affected by either of the freezing treatments upon final thaw, but was significantly reduced over the combined treatment and equilibration phases of the multiple freeze–thaw regimes. Furthermore, the treatments had no significant effects on total or labelled N within the microbial biomass over either phase. Total mesocosm CO
2 efflux rates remained closely correlated with soil temperature throughout the experiment in both regimes, suggesting that respiratory flushes associated with treatment-induced microbial cell lysis were negligible. Together, these results indicate that moderate freeze–thaw fluctuations may have minimal influences on microbial biomass pools, but nevertheless can have strong contrasting effects on the amounts, forms, and timing of N and organic C supply into the soil solution. Ecosystem losses via N
2O effluxes were of greatest magnitude immediately upon thawing in both treatments, and were of similar total magnitude to inorganic N leachates in throughflow. Herb leaves, total fine roots, and vascular stems accumulated some
15N label in one or both of the freezing treatments by the end of the experiment. Together, these results indicating very small N losses relative to the magnitudes of internal transfers, suggest tight ecosystem N cycling both during and after freeze–thaw events. Furthermore, our small and subtle effects on microbial and soluble C and N pools relative to previous studies using more severe regimes, suggests that periods of moderate freeze–thaw fluctuations may have only a minor influence on the annual pattern of C and nutrient dynamics in seasonally cold ecosystems.
$\bullet$ Shrub abundance is expected to increase with enhanced temperature and nutrient availability in the Arctic, and associated changes in abundance of ectomycorrhizal (EM) fungi could be a key ...link between plant responses and longer-term changes in soil organic matter storage. This study quantifies the response in EM fungal abundance to long-term warming and fertilization in two arctic ecosystems with contrasting responses of the EM shrub Betula nana. $\bullet$ Ergosterol was used as a biomarker for living fungal biomass in roots and organic soil and ingrowth bags were used to estimate EM mycelial production. We measured 15N and 13C natural abundance to identify the EM-saprotrophic divide in fungal sporocarps and to validate the EM origin of mycelia in the ingrowth bags. $\bullet$ Fungal biomass in soil and EM mycelial production increased with fertilization at both tundra sites, and with warming at one site. This was caused partly by increased dominance of EM plants and partly by stimulation of EM mycelial growth. $\bullet$ We conclude that cycling of carbon and nitrogen through EM fungi will increase when strongly nutrient-limited arctic ecosystems are exposed to a warmer and more nutrient-rich environment. This has potential consequences for below-ground litter quality and quantity, and for accumulation of organic matter in arctic soils.
The nutritional state of animals is tightly linked to the ambient environment, and for northern ungulates the state strongly influences vital population demographics, such as pregnancy rates. ...Continuously growing tissues, such as hair, can be viewed as dietary records of animals over longer temporal scales. Using sequential data on nitrogen stable isotopes (δ15N) in muskox guard hairs from ten individuals in high arctic Northeast Greenland, we were able to reconstruct the dietary history of muskoxen over approximately 2.5 years with a high temporal resolution of app. 9 days. The dietary chronology included almost three full summer and winter periods. The diet showed strong intra- and inter-annual seasonality, and was significantly linked to changes in local environmental conditions (temperature and snow depth). The summer diets were highly similar across years, reflecting a graminoid-dominated diet. In contrast, winter diets were markedly different between years, a pattern apparently linked to snow conditions. Snow-rich winters had markedly higher δ15N values than snow-poor winters, indicating that muskoxen had limited access to forage, and relied more heavily on their body stores. Due to the close link between body stores and calf production in northern ungulates, the dietary winter signals could eventually serve as an indicator of calf production the following spring. Our study opens the field for further studies and longer chronologies to test such links. The method of sequential stable isotope analysis of guard hairs thus constitutes a promising candidate for population-level monitoring of animals in remote, arctic areas.
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DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
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•Decomposition was studied at surface and in caves along an elevational gradient.•Overall decomposition levels were comparable in above and below ground habitats.•At the surface ...abiotic and biotic factors correlate only with decomposition rate.•In caves abiotic and biotic parameters are associated with stabilizing factor.•Current predictions underestimate the net carbon budget in areas with caves.
Decomposition is a major contributor to ecosystem respiration, determining the carbon emission and nutrient cycling rates. Our current understanding of decomposition dynamics and their underlying drivers has mainly focused on surface habitats but largely ignored in subterranean environments. Here we studied abiotic and microbial drivers of early-stage litter decomposition inside and outside caves along an elevational gradient in Tenerife. We found comparable decomposition rates (k) and litter stabilizing factors (S), with contrasting drivers and elevational variation. At the surface, we observed a mid-elevational trend in k, which tended to correlate with water availability, cooler temperatures, nutrient availability, and surface-specific bacterial taxa. In sharp contrast, caves showed no elevational impact nor influence of abiotic parameters and bacterial communities on k. Despite this, we found higher levels of S in caves, which were associated mainly with reduced water availability, lower temperatures and cave-specific bacterial taxa, indicating that conditions in caves are strongly linked with carbon storage. Our findings imply that our current perception of terrestrial habitat-based carbon cycling are underestimating the net carbon budget in areas with caves. Disentangling the role of the environment on decomposition in caves is key to fully characterize their roles in nutrient cycling and to understand how increasing anthropogenic pressures will affect fundamental processes in subterranean ecosystems.
The subarctic environment of northernmost Sweden has changed over the past century, particularly elements of climate and cryosphere. This paper presents a unique geo-referenced record of ...environmental and ecosystem observations from the area since 1913. Abiotic changes have been substantial. Vegetation changes include not only increases in growth and range extension but also counterintuitive decreases, and stability: all three possible responses. Changes in species composition within the major plant communities have ranged between almost no changes to almost a 50 per cent increase in the number of species. Changes in plant species abundance also vary with particularly large increases in trees and shrubs (up to 600%). There has been an increase in abundance of aspen and large changes in other plant communities responding to wetland area increases resulting from permafrost thaw. Populations of herbivores have responded to varying management practices and climate regimes, particularly changing snow conditions. While it is difficult to generalize and scale-up the site-specific changes in ecosystems, this very site-specificity, combined with projections of change, is of immediate relevance to local stakeholders who need to adapt to new opportunities and to respond to challenges. Furthermore, the relatively small area and its unique datasets are a microcosm of the complexity of Arctic landscapes in transition that remains to be documented.
Aims: Poorly drained arctic ecosystems are potential large emitters of methane (CH₄) due to their high soil organic carbon content and low oxygen availability. In wetlands, aerenchymatous plants ...transport CH₄ from the soil to the atmosphere, but concurrently transport O₂ to the rhizosphere, which may lead to oxidation of CH₄. The importance of the latter process is largely unknown for arctic plant species and ecosystems. Here, we aim to quantify the subsurface oxidation of CH₄ in a waterlogged arctic ecosystem dominated by Carex aquatilis ssp. starts and Eriophorum angustifolium, and evaluate the overall effect of these plants on the CH₄ budget. Methods: A mesocosms study was established based on the upper 20 cm of an organic soil profile with intact plants retrieved from a peatland in West Greenland (69°N). We measured dissolved concentrations and emissions of ¹³CO₂ and ¹³CH₄ from mesocosms during three weeks after addition of ¹³C-enriched CH₄ below the mesocosm. Results: Most of the recovered ¹³C label (>98 %) escaped the ecosystem as CH₄, while less than 2 % was oxidized to ¹³CO₂. Conclusions: It is concluded that aerenchymatous plants control the overall CH₄ emissions but, as a transport system for oxygen, are too inefficient to markedly reduce CH₄ emissions.
Decomposition of Organic Matter in Caves Ravn, Nynne Rand; Michelsen, Anders; Reboleira, Ana Sofia P. S.
Frontiers in ecology and evolution,
10/2020, Letnik:
8
Journal Article
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Decomposition of organic matter is a process, which includes mostly physical breakdown and biochemical transformation of complex organic molecules into simpler organic and inorganic molecules. The ...decomposition of organic matter is an important contributor to ecosystem respiration, which together with photosynthesis controls the net carbon emission from ecosystems. Subterranean ecosystems are extended all over the subsurface of our planet, and lack of light and consequently of photosynthetic activity. Understanding the drivers that control the dynamics of the decomposition processes in the deep subterranean spaces is important because they might differ from those at surface, due to factors as low species diversity and abundance, low microbial biomass, nutrient poor conditions, less pronounced variation of temperature, and higher humidity inside cave. Here, we review the existing studies of organic matter decomposition in caves. Decomposition rates are known from only nine caves representing four biogeographic regions, including Europe, North and South America. Most of the studies were performed in the aquatic compartment of caves. The decay of nine different organic substrates have been followed and the incubation time varied from 36 to 439 days. From a cave located in Australia the mass loss of leaf material from three plant species was investigated after 9 days incubation in the terrestrial compartment of the cave. Based on these observations, litter quality seems to be an important driver of decomposition in caves, and invertebrates have a stimulating effect on the decomposition within individual cave zones. The degree of connection to the surface also influences decomposition rate inside the cave. The lack of standard data among the studies is currently the major impediment to evaluate how differently the process proceeds in the underground compared to the surface, and to disentangle the main drivers of decomposition in caves across biomes. Improving our understanding of organic matter decomposition dynamics in caves will require the standardization of protocols and evaluation of the process over space and time, and a better comprehension on how decomposition changes over latitudinal, altitudinal and depth gradients.
1. Mammalian herbivores can strongly influence nitrogen (N) cycling and herbivore urine could be a central component of the N cycle in grazed ecosystems. Despite its potential role for ecosystem ...productivity and functioning, the fate of N derived from urine has rarely been investigated in grazed ecosystems. 2. This study explored the fate of ¹⁵N-enriched urea in tundra sites that have been either lightly or intensively grazed by reindeer for more than 50 years. We followed the fate of the ¹⁵N applied to the plant canopy, at 2 weeks and 1 year after tracer addition, in the different ecosystem N pools. 3. ¹⁵N-urea was rapidly incorporated in cryptogams and in above-ground parts of vascular plants, while the soil microbial pool and plant roots sequestered only a marginal proportion. Furthermore, the litter layer constituted a large sink for the ¹⁵N-urea, at least in the short term, indicating a high biological activity in the litter in the first phases of organic matter 15 layer and high immobilization decomposition. 4. Mosses and lichens still constituted the largest sink for the ¹⁵N-urea 1 year after tracer addition at both levels of grazing intensity demonstrating their large ability to capture and retain N from urine. Despite large fundamental differences in their traits, deciduous and evergreen shrubs were just as efficient as graminoids in taking up the ¹⁵N-urea. The total recovery of ¹⁵N-urea was lower in the intensively grazed sites, suggesting that reindeer reduce ecosystem N retention. 5. Synthesis. The rapid incorporation of the applied ¹⁵N-urea indicates that arctic plants can take advantage of a pulse of incoming N from urine. In addition, δ¹⁵N values of all taxa in the heavily grazed sites converged towards the δ¹⁵N values for urine, bringing further evidence that urine is an important N source for plants in grazed tundra ecosystems.
If microbial degradation of carbon substrates in arctic soil is stimulated by climatic warming, this would be a significant positive feedback on global change. With data from a climate change ...experiment in Northern Sweden we show that warming and enhanced soil nutrient availability, which is a predicted long-term consequence of climatic warming and mimicked by fertilization, both increase soil microbial biomass. However, while fertilization increased the relative abundance of fungi, warming caused only a minimal shift in the microbial community composition based on the phospholipid fatty acid (PLFA) and neutral lipid fatty acid (NLFA) profiles. The function of the microbial community was also differently affected, as indicated by stable isotope probing of PLFA and NLFA. We demonstrate that two decades of fertilization have favored fungi relative to bacteria, and increased the turnover of complex organic compounds such as vanillin, while warming has had no such effects. Furthermore, the NLFA-to-PLFA ratio for (13)C-incorporation from acetate increased in warmed plots but not in fertilized ones. Thus, fertilization cannot be used as a proxy for effects on warming in arctic tundra soils. Furthermore, the different functional responses suggest that the biomass increase found in both fertilized and warmed plots was mediated via different mechanisms.
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DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK