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Invasive earthworms unlock arctic plant nitrogen limitation


Arctic plant growth is predominantly nitrogen (N) limited. This limitation is generally attributed to slow soil microbial processes due to low temperatures. Here, we show that arctic plant-soil N cycling is also substantially constrained by the lack of larger detritivores (earthworms) able to mineralize and physically translocate litter and soil organic matter. These new functions provided by earthworms increased shrub and grass N concentration in our common garden experiment. Earthworm activity also increased either the height or number of floral shoots, while enhancing fine root production and vegetation greenness in heath and meadow communities to a level that exceeded the inherent differences between these two common arctic plant communities. Moreover, these worming effects on plant N and greening exceeded reported effects of warming, herbivory and nutrient addition, suggesting that human spreading of earthworms may lead to substantial changes in the structure and function of arctic ecosystems.


Nitrogen (N) cycling in arctic soils plays an important role for the global climate system1 as vegetation changes in this biome directly affect the radiative forcing of our planet2,3 and the carbon pool in arctic soils plays a profound role in the terrestrial carbon-climate feedback system4. Arctic plants and microbes are heavily controlled by N availability5,6,7,8,9; hence, disruptions in N cycling can have large consequences for the functioning of tundra ecosystems. Commonly, the low nutrient availability in arctic soils is attributed to the cold climate hampering microbial turnover of nutrient pools10. In line with this view, abiotic drivers such as warming11 or permafrost thaw co-occurring with warming12 have been shown to increase intrinsic N cycling and N availability for tundra plants. Other studies have explored effects of other abiotic drivers, such as increased external inorganic N inputs13,14. Even though biotic drivers of change (e.g., herbivory) have also been acknowledged, no study has so far experimentally quantified potential impacts of invasive soil macrofauna on the intrinsic arctic N cycle—organisms that may provide functions that are currently absent in the decomposition process of tundra soils.

A potentially invasive group of soil macrofauna are earthworms that utilize deeper mineral soil layers (endogeic and anecic species) and thereby transform and restructure nutrient pools in upper soil horizons (henceforth: geoengineering earthworms). Earthworms represent textbook examples of organisms that stimulate N mineralization15, and can cause increased nitrification16 or denitrification due to their gut-associated bacterial community17. By releasing N from organic compounds earthworms stimulate microbial processes18 and plant growth19. Due to their capacity to both transform and restructure N pools, invasion of geoengineering earthworms into pristine tundra, where they are currently absent, may have substantial effects on arctic soils. Past glaciations eradicated geoengineering earthworms from arctic soils and their slow natural dispersal rates, 5–20 m yr−120,21, could leave high latitude landscapes without earthworms even over a Holocene time-scale—if not assisted by human mediated dispersal. Despite slow natural dispersal rates, human mediated introduction of earthworms into formerly glaciated landscapes may lead to near complete colonization over a decadal to centennial time-scale21,22. Observations also show that geoengineering earthworms, when introduced by humans, have established in arctic soils encompassing North America, Greenland, Iceland, Fennoscandia, and Russia (Fig. 1). Further, global warming is expected to facilitate survival and establishment of southern invaders, such as earthworms, both because of predicted improved abiotic conditions and due to the increasing number of human-mediated dispersal vectors that accompany intensified land-use in the Arctic23. Increasing soil temperatures and predicted formation of year-round unfrozen soil layers (talik) in the near future24 offer examples of potential niches opening in areas where frozen soils have previously limited earthworm establishment. In addition, recent models assessing both soil properties as well as climatic conditions predict that large areas in the Arctic are already suitable for several earthworm species25. In other ecosystems, some plants can be negatively affected by earthworm activities26, which makes the impact of geoengineering earthworms in tundra plant–soil systems largely speculative given the current lack of empirical studies.

Fig. 1: Documented presence of geoengineering earthworms in the Arctic.

Sites (red circles) in which Lumbricus sp. and Aporrectodea sp. have been found (utilizing the mineral soil as a habitat) in the arctic biome (purple shading) divided into three major geographical zones (sub-, low-, and high-arctic). Sites are compiled from previously published studies27,47,49,52,53,54,55 and findings presented in the Global Biodiversity Information Facility database. Red rectangle indicates a reported finding of L. rubellus in Greenland where the specific site was not reported56. The figure does not intend to provide a complete overview of known populations of geoengineering earthworms, but to illustrate that they can survive in the Arctic (mainly the sub-arctic zone). A common denominator is that earthworms occur adjacent to human introduction points. Thus, the map illustrates that human mediated introductions occur at circumpolar scale. The underlying map showing geographic areas of the Arctic is derived from the Arctic Biodiversity Assessment (

Here, we study two species that represent geoengineering earthworms (Lumbricus sp. and Aporrectodea sp.) which, once introduced by humans, can establish in the Arctic (Fig. 1) and reshape the arctic soil morphology in our study region in northern Sweden27. We use an arctic common garden experiment conducted over two growing seasons (Supplementary Fig. 1, Supplementary Table 1) consisting of two vegetation types (heath and meadow) supplemented with 15N labeled litter. In this setting, we applied geoengineering earthworms to assess their effect on N cycling in dwarf shrub- and forb dominated tundra communities. We hypothesize that, by providing currently missing functions in the decomposition process, these earthworms increase plant N uptake. In addition, we hypothesize that positive effects on plant N uptake are sufficient to enhance plant growth.


Earthworm effects on plant N uptake

Plant N concentration and N sources of the five studied plant species changed already in the first growing season with geoengineering earthworm presence. Without earthworms present, N concentration of the grass Festuca ovina, the only species common in both plant communities, did not differ between heath (dwarf shrub dominated) and meadow (forb dominated). However, with earthworms present N concentration in F. ovina increased on average by 50% (F1,6 = 43.3, P < 0.001, Fig. 2), more strongly so in the heath than in the meadow (vegetation × earthworm F1,24 = 5.6, P = 0.025; Fig. 2). Both the earthworm additions (F1,6 = 20.9, P = 0.004) and isotopic labeling of the litter layer (F1,24 = 57.1, P < 0.001) induced a significantly higher δ15N in F. ovina (Fig. 2). In addition, there was a significant interactive effect of earthworm and litter labeling treatment on δ15N in F. ovina (F1,30 = 4.7, P = 0.039), showing that more N from the litter pool was used by F. ovina when earthworms were present.

Fig. 2: Earthworm effects on nitrogen uptake of Festuca ovina.

Shown are earthworm effects on N content (%) and δ15N of Festuca ovina, a plant present in both of the studied vegetation types, i.e., heath (H) and meadow (M). Individual replicates of samples from unlabeled (white diamond shape) and δ15N labeled (red circle, where darker values indicate overlapping data) mesocosms are shown with average values (black square, ±std. err). Main effects and interaction effects are presented as text for each panel (effect of the labeled litter is indicated using the 15N symbol) along with symbols indicating significance level (P < 0.05 are shown using *, and significance levels <0.001 are indicated as ***). Note the cut off in the y-axis to show the δ15N signatures of the unlabeled and the labeled litter. Source data are provided as a Source Data file.

The analyses of four additional plant species that were specific to one of the two vegetation types further indicated that earthworms increase the N concentrations in plants. Of the species only present in the heath vegetation, in addition to F. ovina, Vaccinium vitis-idaea had higher N concentrations in the presence of earthworms (F1,6 = 13.7, P = 0.010) and while Vaccinium myrtillus responded in a similar way as V. vitis-idaea and F. ovina, the difference was not statistically significant (F1,6 = 5.6, P = 0.055) (Fig. 3). Similar to the effects on F. ovina reported above, the increased plant N in the habitat-specific species was also derived at least partly from the litter layer; the δ15N of Saussurea alpina did not differ between labeled and unlabeled litter additions without earthworms, but it increased with earthworms (labeling × earthworm, F1,14 = 4.7, P = 0.048) (Fig. 3). No other of the plants specific to the two vegetation types showed this interaction effect (Supplementary Table 4).

Fig. 3: Earthworm effects on nitrogen uptake of common heath and meadow species.

Nitrogen content and δ15N signatures of dwarf shrubs found only in heath (V. vitis-idea and V. myrtillus) and forbs found only in meadow (S. alpina and B. viviparia) in response to geoengineering earthworms. Note that these plant species were only found in one of the two vegetation types and thus did not allow comparison of effects between vegetation types. Individual replicates of samples from unlabeled (white diamond shape) and δ15N labeled (red circle, where darker values indicate overlapping data) mesocosms are shown with average values (black square, ±std. err). Main effects and interaction effects are presented as text for each panel (effect of the labeled litter is indicated using the 15N symbol) along with symbols indicating significance level (P < 0.05 are shown using *, and significance levels <0.001 are indicated as ***). Note the cut off in the y-axis to show the δ15N signatures of the unlabeled and the labeled litter. Source data are provided as a Source Data file.

There was no earthworm effect on the gravimetric (measured only during the first growing season) or volumetric soil moisture (first season). However, the volumetric soil water content (measured continuously with loggers) suggested a difference between the vegetation types (F1,9 = 16.4, P < 0.01) and the seasonal average water content was higher in the meadow (0.23 m3/m3) than in the heath (0.02 m3/m3). Analyses of litter cover, soil nutrients—using plant root simulator (PRS) probes—and microbial community—using phospholipid fatty acid (PLFA) analysis—after the first season provided additional insights about the processes driving plant N uptake in the presence of earthworms (Table 1). Earthworms reduced the surface litter cover, yet only in the meadow (vegetation × earthworm; F1,38 = 7.9; P = 0.008), but we detected a vertical mixing of surface litter into the rooting zone in the form of belowground earthworm tunnels and castings in both vegetation types (Supplementary Fig. 2). The PRS probes revealed no significant differences caused by earthworms in the availability of soluble inorganic N fractions (NO3 and NH4) and other key macronutrients such as phosphorous, base cations, iron and manganese (Supplementary Fig. 2). Nevertheless, in a complementing leaching study (see Methods) analyses of water soluble N forms showed that N mineralization was profound in the earthworm casts. Fresh casts (<7 days old) were dominated by inorganic N and had an NH4 concentration >10,000% higher than “earthworm free” litter and humus that were dominated by organic N forms (Supplementary Fig. 3). Nitrate concentrations were minute in comparison to NH4 in casts, litter, and humus. The PLFA analysis from the samples collected from the upper 10 cm horizon (including litter and soil), suggested that earthworms reduced bacterial biomass in the meadow, but not in the heath (vegetation × earthworm; actinomycetes: F1,38 = 4.6, P = 0.039; other bacteria: F1,38 = 4.8, P = 0.035), and had no effect on fungal biomass in either of the habitats (F1,38 = 0.8, P = 0.358). The biomass of actinomycetes, other soil bacteria and fungi was higher in the meadow than in the heath (Table 1, actinomycetes: F1,38 = 38.7, P < 0.001; other bacteria: F1,38 = 26.6, P < 0.001; fungi: F1,30 = 10.4, P = 0.002).

Table 1 Effects of geoengineering earthworms on litter cover and microbial and plant communities.

Earthworm effects on above and belowground plant production

Within the first season after earthworm introduction, the normalized difference vegetation index (NDVI, a measure of greenness) was significantly higher when earthworms were present (F1,6 = 6.4, P = 0.045; Table 1), while abundances of graminoids, forbs, deciduous dwarf shrubs, evergreen dwarf shrubs, mosses, and lichens did not change in response to earthworms (Supplementary Table 3). After the second season with earthworms, the maximum height of floral shoots of Deschampsia flexuosa was about three times higher when earthworms were present in the meadow (vegetation × earthworm; F1,38 = 9.3, P = 0.004) while the number of floral shoots remained similar between treatments (Fig. 4a, b). In contrast, the number of floral shoots of F. ovina was greater in the presence of earthworms (F1,6 = 4.7, P = 0.043). As would be expected if plant N availability was driving the observed growth responses, the N-content of F. ovina correlated positively with the number of floral shoots (R2 = 0.518, P = 0.001). In addition, the N content of F. ovina correlated positively with the NDVI of the studied plant communities (R2 = 0.487, P = 0.002).

Fig. 4: Aboveground plant growth responses to earthworm additions.

Boxplot showing a the maximum height and b the highest number of floral shoots (lower panel) of graminoids (D. flexuosa and F. ovina) per mesocosm. Diamond box indicate the 25%- to 75%-percentiles (whiskers show 99% percentile) and black rectangle the median value. Mesocosms lacking the studied plants are given a value of 0. Significant effects are indicated with *(P < 0.05). Source data are provided as a Source Data file.

At the onset of the experiment (13 June 2017, Supplementary Table 1), total fine root length did not differ between the vegetation types or between the earthworm treatments (Fig. 5). After 55 days, fine root growth was higher in meadow including earthworms than in meadow without earthworms (vegetation × earthworm; F1,6 = 4.5, P = 0.042). After 103 days, fine root growth in both vegetation types was almost twice as high under earthworm presence than without earthworms (F1,6 = 8.3, P = 0.028).

Fig. 5: Belowground plant growth response to earthworm additions.

Boxplot showing the fine root length at the onset of the experiment before the earthworm addition, and the fine root growth after earthworm addition in heath and meadow vegetation (mesocosm with labeled and unlabeled litter are pooled together). Periods when growth was measured are shown at the top. Diamond box indicate the 25%- and 75%-percentile (whiskers indicate the 99% percentile) and black rectangle show the median value. Also shown are all individual measurements (red diamonds). Treatment effects are written at the base of the panels and the level of significance indicated with *(P < 0.05) and **(P < 0.01). Source data are provided as a Source Data file.


Our results suggest that geoengineering earthworms and their activity increase plant N uptake from tundra soils, as earthworm presence increased plant N content, altered the δ15N of plant leaves, and boosted fine root growth already within the first season. The increased uptake of N was associated with increased individual plant height and amount of floral shoots and this enhanced performance of individual plants was also accompanied by community level increased NDVI (a measure of vegetation greenness). The most likely driver behind these effects is a boosting of N mineralization processes by earthworms, a process identified both by previous laboratory experiments28 as well as our comparison of NH4 in earthworm casts, litter and humus (Supplementary Fig. 4).

Geoengineering earthworms doubled leaf tissue N concentrations in F. ovina—an effect larger than the difference seen in this species caused by the growth conditions in the two studied vegetation types—and, thus appear at least as important as the dwarf shrub- and forb-driven effects currently dictating N cycling in tundra ecosystems29,30. Given the strong N limitation in arctic systems5,7,9 the increased plant N uptake triggered by earthworms is, indeed, expected to increase above- and belowground plant growth (hypothesis 2). Yet, the near doubling in fine root growth in fall and the more than doubling in length of D. flexuosa and number of shoots of F. ovina that we observed are surprisingly strong compared to the inherent differences between the studied dwarf shrub and forb vegetation communities. The effects we observed on root growth and above ground biomass were also strong compared to North American forests, where earthworms can even have negative effects on fine root growth31, and to agricultural systems where earthworms cause on average 23% increase in aboveground biomass19. Similar to manipulations of abiotic factors such as nutrients and temperature32 some of the effects of earthworms on plants seem species-specific. Some species increased N uptake in the presence of earthworms (F. ovina, V. vitis-idaea), while others (S. alpina) only changed their N sources as indicated by the changes in δ15N. Similarly, growth responses to earthworms also seem species specific since D. flexuosa increased in length of floral shoots, while F. ovina produced more of them. This asymmetric response between species suggests that if these plant responses are permanent, tundra plant communities could change in the long-term, possibly increasing the abundances of graminoids as seen in earthworm invaded North American forests26.

The effects of earthworms on fine root production in dwarf shrub and forb communities were notably stronger than the effects seen in local warming experiments, simulating autumn warming33 or variation in climatic conditions prevailing along a 500 m elevation gradient34. To further illustrate the importance of geoengineering earthworms in comparison to other environmental factors/drivers in our study area, we extracted plant community N (a weighted average N content calculated using coverage of plant functional groups as weights) and NDVI data (vegetation greenness) from previous local studies. These were situated in comparable vegetation settings within the same region (<20 km from our experiment) reducing any bias caused by context-dependent responses (Supplementary Tables 3 and 5). This comparison revealed that the effects on N content and NDVI caused by geoengineering earthworms were as strong, or even stronger, than other important environmental drivers in the Arctic, including warming, herbivory and fer tilization (Fig. 6a, b). For example, earthworms increased plant community N concentrations over three times as much as a 3 °C increase in summer temperatures35,36 or extensive fertilization with reindeer feces37. Moreover, the increases in NDVI caused by the earthworms were similar to the differences in greenness caused by a 3 °C warming along natural elevation gradients and more substantial than effects of herbivory and fertilization (Fig. 6b). Even expanding our comparison from local experiments to large-scale datasets further suggests that the worming effect on NDVI and community N is substantial compared to the effects of warming. Plant community N increased by about 30% in the presence of earthworms in our study, which is larger than the average 15% increase in response to summer warming from mean temperatures of 3–10 °C occurring across the arctic biome38. The earthworms also caused an increase in NDVI of 0.02–0.04 units (corresponding to 3–5% change) in our study, which is comparable to the greening accompanying shrub expansion and increased plant growth during the last decades in the Arctic (typically between 0.17 and 0.84% yr−1 increase in NDVI)39,40.

Fig. 6: Effects of earthworms compared to other environmental drivers in a changing Arctic.

Shown are a conceptual comparison of effects (percentage change relative to average of control) caused by earthworms (worming) with effects seen in previous local experiments in sub-arctic northern Sweden simulating arctic environmental change including warming, herbivory, and fertilization. a Effects (mean ± std. err) on plant community N expressed as a function of vegetation type (BF = sub-arctic birch forest, H = heath, and M = meadow). Nitrogen data for warming are from open top chambers35 and from an alpine altitudinal gradient36, the herbivory experiment was conducted using fences excluding voles and reindeer (shown effects are illustrating when grazers are present in relation to the ungrazed control)35 and reindeer feces were used in the fertilization experiment, where additions corresponded to about double and four times natural abundance37. b Effects (mean ± std. err) on NDVI (i.e., greenness) expressed as a function of vegetation type. Experiments are similar as above with the addition of data from an open top chamber experiment simulating a mean annual temperature increase of 1 °C conducted at both an altitude of 500 and 900 m.a.s.l. Source data are provided in Supplementary Table 3, Supplementary Methods 1 and as a Source Data file.

Earthworms boost the plant N uptake through two apparent processes in our study. Firstly, by stimulating mineralization of litter and humus into NH4-enriched casts; and secondly by vertically translocating nutrients from aboveground litter and fertile casts into the rooting zone so that they become more accessible for plants. Firstly, earthworms boost mineralization strongly in arctic soils as verified by their casts that had NH4 concentration >10,000% higher than the bulk soil (Supplementary Fig. 3)—importantly, this enrichment is one magnitude higher than observed in agricultural ecosystems41. Secondly, earthworms facilitate plant use of N from aboveground plant litter as revealed by decreased litter cover and a change in plant–δ15N toward the signature of the labeled litter. Indeed, an increased importance of litter derived N is expected from geoengineering earthworms considering their ability to mineralize litter, but also annual mixing ~0.6 cm of the surface soil into deeper soil layers42. We confirmed this mixing to be an active process in our tundra experiment by observing reduced litter cover in the meadow (forb dominated) in parallel with deposition of earthworm casting directly within the rooting zone (Supplementary Fig. 2). Because the increases in plant N concentrations do not fully match the increases in δ15N, also other, older soil N pools were mobilized and deposited as casts—especially in the heath (dwarf shrub dominated) where litter cover decreased less evidently. We acknowledge that dead and decomposing earthworms could be an additional N source in the experiment (as also under field conditions), but we do not believe this is a major contribution for two reasons. Firstly, the N taken up by plants was, at least partly, derived from plant litter. Secondly, our belowground imaging revealed living earthworms and formation of earthworm tunnels at the same time as positive effect on plant N uptake occurred, which was during both the peak and late growing season prior to the first winter of our experiment when soil–frost induced mortality is expected.

The mobilization of N from aboveground litter and the high availability of mineral N in earthworm casts (as measured in the leaching study) were associated with a higher plant N content, although we did not record any increases in mineral N in the PRS probes targeting the in situ soil solution. This is likely caused by a rapid plant uptake of the N made available by the earthworms, resulting in little N diffusion through the soil solution to the PRS probes. These results corroborate previous studies showing that N from urine and droppings of reindeer can increase plant N uptake and growth without any measurable effects on soil N availability43,44,45. While plant N concentrations and growth showed strong positive responses to the earthworms in both vegetation types, microbial biomass increased with earthworm presence in the heath and decreased in the meadow. We acknowledge that these observed microbial effects could be linked to both a direct effect of earthworms resulting in different responses among types of microbes, or indirect effects where the microbial community responds to changes in soil organic matter quality and the observed plant community specific effects on fine root growth. Considering the earlier response in fine root growth in the meadow, fiercer plant competition for N during the summer seems as a plausible process contributing to reduced microbial biomass in these plant communities.

The finding of a strong positive effect of geoengineering earthworms on plant N uptake is an important advancement in our understanding of plant N limitation in tundra soils. It shows that plant uptake of N from litter and soil pools can be greatly enhanced by introducing detritivores that are able to accelerate mineralization of organic matter and excrete processed material, casts, into the rooting zone. To synthesize, the absence of these functions represents a strong bottleneck in the plant N cycle in the Arctic. Our findings do not contradict the current view that the N (and carbon) cycle is constrained by temperature dependent microbial processes, but add a new central process—a great boost in the intrinsic N cycle can be achieved by changes in the soil macrofauna alone, without any direct impact of temperature per se. This increased knowledge is important as it implies that any mechanistic model predicting future changes in the arctic N cycle and subsequent effects on greening, plant communities or carbon cycling, needs to consider dispersal scenarios for soil macrofauna adding novel functions into the current decomposition process in tundra soils. By unlocking the physical entrapment of nutrients, occurring both at a vertical scale (above the rooting zone) and within soil organic matter that can be mineralized inside the earthworm gut, geoengineering earthworms provide plants access to new nutrient pools. Conceptually, this effect can be compared with processes generated during permafrost thaw, where thawing soil layers release soil nutrient pools previously unaccessible for plant roots which is recognized to have a strong impact on the plant N cycle12. However, in contrast to permafrost thaw, where effects are generated at greater soil depths and thus primarily affect deep-rooted plants46, geoengineering earthworms affect nutrient cycling within the upper few decimeters of soil where most plants have already allocated their roots. That geoengineering earthworms survive in discontinuous permafrost zones of Scandinavia, Russia, and North America when introduced by humans27,47,48,49, shows that suitable habitats already exist in the Arctic, and highlight that their lagged northward dispersal needs to be considered when fully understanding long-term nutrient cycling at high latitudes. The demonstrated strong effects on the tundra plant N uptake by geoengineering earthworms show that natural or human-aided dispersal of novel, large detritivores into tundra soils can have substantial impacts on the tundra ecosystem. From human-mediated invasions in other environments, we know that near complete (>80%) colonization of suitable habitats can occur over a decadal to centennial time-scale due to multiple introduction points22, indicating that earthworm invasions can proceed over a time-scale similar to that of climate change. Importantly, expected impacts from invasive earthworms on the plant–soil N cycle exceed those generated by climate warming and other currently recognized drivers of environmental change in this biome.


Study site

This study was conducted at the Abisko Scientific Research Station (68°21′17.0′′ N; 18°48′54′′ E) about 200 km north of the Arctic Circle. The station is located within the sporadic permafrost zone, with a mean annual temperature around 0 °C and mean annual precipitation of 335 mm (1981–2010, Abisko Scientific Research Station, 380 m.a.s.l).

Common garden experiment

We established a mesocosm (N = 48) experiment in the experimental garden of the Abisko Scientific Research Station. An overview of the experimental design is shown in Fig. S1 and a timeline for all activities is shown in Table S1. The mesocosm experiment consisted of natural tundra vegetation–soil monoliths from two vegetation types (meadow and heath) installed during the autumn of 2013. Monoliths for the mesocosms were collected in the Kärkevagge valley, about 20 km northwest of Abisko, Sweden, (at around 68°24′36′′ N; 18°19′11′′ E) at about 700 m elevation. Here, we selected representative patches of both heath and meadow vegetation. The heath was dominated by dwarf shrubs (Empetrum hermaphroditum, V. myrtillus, V. vitis-idaea), with a considerable amount of graminoids (Carex bigelowii, Deschampsia flexuosa, Festuca ovina) and bryophytes (Pleurozium schreberi, Hylocomium splendens). The meadow was dominated by forbs (Alchemilla glomerulans, Bistorta vivipara, S. alpina) and graminoids (C. bigelowii, D. flexuosa, F. ovina). Soils were pooled by vegetation type and homogenized to ensure a similar depth of soil under each vegetation patch regardless of their original soil depth. Mesocosms were constructed using polypropylene plastic boxes (50 × 39 × 30 cm, with 10 drainage holes with a diameter about 1 cm at the bottom) with a layer of weed cloth, a fine layer (c. 1 cm) of sand, and the mixed heath or meadow soil (intact vegetation including organic sods of 8 cm, placed on top of an Ah mineral soil horizon of 22 cm). The thickness of the O horizon are typical to that of local soils prior to earthworms invasions27. Average soil organic matter content for the upper 10 cm for the heath and meadow mesocosm were 12.1 ± 0.8% (mean ± std err) and 11.4 ± 1.3%, respectively.

In the common garden, eight wooden raised beds (300 cm × 160 cm, 40 cm high) were prepared, insulated with 5 cm thick styrofoam and filled with sand. The mesocosms were then installed into the raised beds at a randomly determined location. Either five or seven mesocosms were installed per raised bed and these mesocosms presented both heath and meadow vegetation in each bed at approx. equal numbers. The soil surface of the mesocosm was levelled with the surrounding sandy beds to maintain realistic soil temperature fluctuations. The mesocosms were allowed to recover from disturbance between the summer of 2013 and spring 2017 prior to the onset of the experiment. During the experiment soil temperature (−1 cm) and volumetric soil moisture content (down to −10 cm) were recorded at an hourly interval using data loggers (Em50 ECH2O) equipped with temperature (EC-5) and soil moisture (ECT) sensors (Decagon Systems, Washington state, US). See Supplementary Fig. 1 for location of loggers.

Earthworm treatments

Earthworms were first introduced to the mesocosms on 9th of June 2017 at relevant densities. The earthworm species’ used (Aporrectodea sp. and Lumbricus sp.) are observed to radiate out from anthropogenic sources in the surrounding arctic environment with four known invasion sites situated within 12 km from our mesocosm experiment27. All earthworms used in this experiment were collected manually in forest adjacent to farmlands within the municipality of Umeå (63°50′17.7′′ N; 20°18′46′′ E), Sweden. In each mesocosm, we added a total earthworm fresh weight of 24.2 g ± 0.3 (mean ± SE) of endogeic Aporrectodea sp. (Aporrectodea trapezoids, Aporrectodea tuberculata, Aporrectodea rosea, 16–17 individuals per mesocosm) and epi-endogeic Lumbricus rubellus (27–29 individuals per mesocosm), corresponding to densities of 87 and 140 individuals m−2, respectively. As a comparison, measured earthworm densities dominated by Aporrectodea sp. frequently exceed 200 individuals m−2 in nearby (<12 km) arctic earthworm invasion gradients27. One day prior to worm addition, all mesocosms were watered with 10 L each (corresponding to 51 mm precipitation), to prevent desiccation of earthworms directly after release. To prevent earthworms from migrating into mesocosms designated as earthworm-free controls, we assigned whole raised beds as either earthworm addition or controls resulting in four raised beds with and four without earthworms.

In contrast to invasive earthworms populations currently thriving in the local sub-arctic environment27, the earthworms in the mesocosm were unable to migrate below a soil depth of 30 cm. Given that no behavior based strategies could be adopted to cope with the low winter temperatures (down to −15 °C in the mesocosm) and soil frost in the 0.3 m deep mesocosms (soil frost extended down to 1 m during the first winter according to data from Abisko research station, measured <100 m from the experiment), eradication of the earthworm population during winter was considered unavoidable. Therefore, addition of earthworms was repeated in the following season (2018) to assure presence of living individuals. Here, we added earthworms to each mesocosm, corresponding to a fresh weight of 11.7 ± SE 0.3 g on 16 June 2018, to compensate for winter mortalities.

Addition of 15N labeled litter

To assess eventual impact of plant uptake of N from the litter layer, we introduced 15N labeled coarsely ground plant material (12 g) into half of the mesocosms on 19 June 2017 to isotopically spike the litter layer, while the remaining mesocosms received similarly ground but unlabeled litter (12 g). The litter added was a mixture of plant litter from meadow and heath vegetation with very similar species composition as the one used in this study43. The added litter had an atom % 15N of 0.36 ± 0.00 (unlabeled control, average ± SE) and 0.73 ± 0.00 (labeled litter), and a δ15N of −4.89 ± 0.31 (unlabeled control) and 984.44 ± 12.11 (labeled litter). Besides the 15N composition, there was no major difference in the N content between the two litter types (unlabeled: 0.97 ± 10% and labeled 0.88 ± 0.01%).

Plant–root-simulator probes

We used PRSTM soil probes (Western Ag Innovations Inc., Saskatoon, Canada), commercially manufactured ion-exchange membranes, to assess availability of inorganic forms of nitrogen (NO3–N and NH4–N, as well as Ca, Mg, K, P, Fe, and Mn). We installed two pairs in each mesocosm which were pooled before extraction. PRS-probes were buried from 16 June 2017 to 3 October 2017 at a depth of 4–10 cm.

Soil sampling

We collected soil samples to analyze the effects of earthworms on the microbial community composition on the 18 August 2017. From each mesocosm, a composite soil sample was taken by coring to 10 cm depth (four cores, corer diametre 1 cm), including the litter layer but removing the mineral soil horizon and pooling these samples together per mesocosm. In the laboratory, plant roots and litter were manually removed from each composite sample, a sub-sample was analyzed for soil moisture (105 °C, 18 h) and organic matter content (475 °C, 4 h) and the remaining soil sample was frozen (−20 °C) within four days of sampling and consequently freeze dried for PLFA analyses, conducted at the Biogeochemical Analyses Laboratory at the Swedish University of Agricultural Science, Umeå. PFLA analyses are reported in nmol/g dry soil.

Plant foliar nutrient content analyses

We collected green foliage from two to three plant species in each mesocosm at the end of the growing season (21 August 2017). From the meadow mesocosms, we collected the leaves of the two forbs that were present in the highest fraction of the meadow mesocosms; i.e., S. alpina and B. vivipara. From the heath mesocosms, we collected the leaves and stems of two dwarf shrub species, which were found in the highest fraction of the heath mesocosms, i.e., V. vitis-idaea and V. myrtillus. From both vegetation types, we collected the leaves of a jointly common graminoid; F. ovina. Thereby, our leaf samples at each vegetation type represented plant species constituting on average 60% of the vegetation cover. Since present in both vegetation types, F. ovina allowed comparison of plant N acquisition between heath and meadow without the interference caused by interspecific variation. Within each mesocosm, we collected ≥ten leaves of randomly distributed plants with fully expanded green leaves. All collected material was immediately air-dried ≥22 °C. Leaves were sorted from stems (V. myrtillus and V. vitis-idaea), dried (approximately 48 h, 60 °C) and milled into a fine powder (Bertin precellys 24). The ground materials were subsequently analyzed for total N and δ15N (Isotope ratio mass spectrometer DeltaV, Thermo Fisher Scientific, Bremen, Germany; and Elemental analyzer Flash EA 2000, Thermo Fisher Scientific, Bremen, Germany).

Aboveground plant sampling

In 27 July 2017, a vegetation and litter survey was conducted by the point intercept method50 in all mesocosms. We used two 50-cm wide rows of ten vertical pins at every 10 cm and counted the total number of times each species was intercepted by 20 pins. The total number of hits was normalized to hits per 100 pins in each mesocosm. This data were further used to calculate the abundance of plant functional groups (graminoids, forbs, evergreen, and deciduous dwarf-shrubs, mosses, and lichens) at the mesocosm level. For each mesocosm, we also measured NDVI (Normalized Difference Vegetation Index) from 0.5 m above each mesocosm using a hand-held pole and two channel sensors (SKR 1800D/SS2, SKL925 logger, SpectroSense2, Sky Instruments, Llandrindon Wells, Wales UK). This index measures the differences between near-infrared light (which vegetation strongly reflects) and red light (which vegetation absorbs), where higher values are indicative of higher photosynthetic activity for the plant community (used as a measure of vegetation greenness).

As an additional proxy for plant growth, we measured the length of the highest individuals and floral shoot numbers of F. ovina, and D. flexuosa (species that occurred in most of the mesocosms) in late autumn of 2018.

Below ground plant production

Total fine root length and fine root growth were measured on 13 June, 7 August, and 25 September 2017 using minirhizotrons (Bartz Technology Corporation, Carpinteria, CA, USA), a nondestructive method for observing temporal development of fine roots. These are transparent tubes with an inner diameter of 5 cm, which were placed horizontally at a depth of 10 cm into the mesocosms during their initial installation.

Nitrogen in earthworm products

To assess mineralization and nitrification rates in earthworm casts in comparison to litter and humus we conducted a water leaching experiment. All material was collected in situ from the earthworm invasion gradient at Jiebren, situated <10 km from the mesocosm experiment, described in detail elsewhere27. Fresh excreted casts were gathered from collected earthworms (Aporrectodea sp.) excreting cast directly into vials, while aged earthworm casts deposited during the season on top of litter was collected manually from the soil surface of forb and dwarf shrub vegetation communities growing under sparsely growing sub-alpine birch forest. Litter and humus (sieved through a 2 mm mesh) from meadow and heath vegetation communities was obtained from uninvaded soil behind a stream functioning as a migration barrier27. Sampled material was homogenized and subsectioned. One sub-sample was shaken in Milli Q water (sample v-water v, 1:5) for 2 h, centrifuged at 4000 rpm and the supernatant filtered through a 0.2 µm filter to remove bacteria. Sample was directly frozen after filtering and analyzed for inorganic N using a segmented flow analyzer (QuAAyro39, Seal Analytica) and total N was measured using a Formacs HT-I (Skalar) with a mounted nitrogen detector (ND 25). Organic N was calculated by subtracting the inorganic N from the total N.


The effect of earthworms, vegetation type and 15N labeling of litter (labeled and unlabeled) on plant N concentrations, plant δ15N, soil nutrient availability, abundance of bacteria, fungi, litter, and plant functional types and height of graminoids was tested with a linear mixed effect model using the lme command from the nlme package51 within the statistical environment R (R Core Team 2018). Earthworm treatment, vegetation type, and 15N labeling was treated as fixed categorical factors and block was treated as a categorical random factor to account for the spatial autocorrelation within blocks. Heteroscedasticity was tested by inspecting residuals and data was log transformed in a few cases to achieve homoscedasticity. The number of floral shoots was tested using the glmmPQL function in the statistical package MASS (Venables & Ripley 2002) within the statistical environment R (R Core Team 2018).

Data availability

The source data underlying results shown in Figs. 2–6 are provided as a Source Data file, and uploaded on figshare [].


  1. 1.

    Arneth, A. et al. Terrestrial biogeochemical feedbacks in the climate system. Nat. Geosci. 3, 525–532 (2010).

    ADS  CAS  Article  Google Scholar 

  2. 2.

    Chapin, F. S. et al. Role of land-surface changes in Arctic summer warming. Science 310, 657–660 (2005).

    ADS  CAS  PubMed  Article  Google Scholar 

  3. 3.

    Pearson, R. G. et al. Shifts in Arctic vegetation and associated feedbacks under climate change. Nat. Clim. Chang. 3, 673–677 (2013).

    ADS  Article  Google Scholar 

  4. 4.

    Schuur, E. A. G. et al. Climate change and the permafrost carbon feedback. Nature 520, 171–179 (2015).

    ADS  CAS  PubMed  Article  Google Scholar 

  5. 5.

    Sistla, S. A., Asao, S. & Schimel, J. P. Detecting microbial N-limitation in tussock tundra soil: implications for Arctic soil organic carbon cycling. Soil Biol. Biochem. 55, 78–84 (2012).

    CAS  Article  Google Scholar 

  6. 6.

    Wild, B. et al. Microbial nitrogen dynamics in organic and mineral soil horizons along a latitudinal transect in western Siberia. Glob. Biogeochem. Cycle 29, 567–582 (2015).

    ADS  CAS  Article  Google Scholar 

  7. 7.

    McKane, R. B. et al. Resource-based niches provide a basis for plant species diversity and dominance in arctic tundra. Nature 415, 68–71 (2002).

    ADS  CAS  PubMed  Article  Google Scholar 

  8. 8.

    McMahon, S. & Schimel, J. P. Shifting patterns microbial N-metabolism across seasons in upland Alaskan tundra soils. Soil Biol. Biochem. 105, 96–107 (2017).

    CAS  Article  Google Scholar 

  9. 9.

    Chapin, F. S., Moilanen, L. & Kielland, K. Preferential use of organic nitrogen for growth by a nonmycorrhizal arctic sedge. Nature 361, 150–153 (1993).

    ADS  CAS  Article  Google Scholar 

  10. 10.

    Hobbie, S. E. Temperature and plant species control over litter decomposition in Alaskan tundra. Ecol. Monogr. 66, 503–522 (1996).

    Article  Google Scholar 

  11. 11.

    Sistla, S. A. et al. Long-term warming restructures Arctic tundra without changing net soil carbon storage. Nature 497, 615 (2013). +.

    ADS  CAS  PubMed  Article  Google Scholar 

  12. 12.

    Chen, L. et al. Nitrogen availability regulates topsoil carbon dynamics after permafrost thaw by altering microbial metabolic efficiency. Nat. Commun. 9, 3951 (2018).

    ADS  PubMed  PubMed Central  Article  CAS  Google Scholar 

  13. 13.

    Song, M. H. et al. Shifts in priming partly explain impacts of long-term nitrogen input in different chemical forms on soil organic carbon storage. Glob. Change Biol. 24, 4160–4172 (2018).

    ADS  Article  Google Scholar 

  14. 14.

    Mack, M. C., Schuur, E. A. G., Bret-Harte, M. S., Shaver, G. R. & Chapin, F. S. Ecosystem carbon storage in arctic tundra reduced by long-term nutrient fertilization. Nature 431, 440–443 (2004).

    ADS  CAS  PubMed  Article  Google Scholar 

  15. 15.

    Lavelle, P. Faunal activities and soil processes: adaptive strategies that determine ecosystem function. Adv. Ecol. Res.27, 93–132 (1997).

    Article  Google Scholar 

  16. 16.

    Szlavecz, K. et al. Invasive earthworm species and nitrogen cycling in remnant forest patches. Appl. Soil Ecol. 32, 54–62 (2006).

    Article  Google Scholar 

  17. 17.

    Lubbers, I. M. et al. Greenhouse-gas emissions from soils increased by earthworms. Nat. Clim. Chang. 3, 187–194 (2013).

    ADS  CAS  Article  Google Scholar 

  18. 18.

    Parkin, T. B. & Berry, E. C. Microbial nitrogen transformations in earthworm burrows. Soil Biol. Biochem. 31, 1765–1771 (1999).

    CAS  Article  Google Scholar 

  19. 19.

    van Groenigen, J. W. et al. Earthworms increase plant production: a meta-analysis. Sci. Rep. 4, 7 (2014).

    Google Scholar 

  20. 20.

    Frelich, L. E. et al. Earthworm invasion into previously earthworm-free temperate and boreal forests. Biol. Invasions 8, 1235–1245 (2006).

    Article  Google Scholar 

  21. 21.

    Chkrebtii, O. A., Cameron, E. K., Campbell, D. A. & Bayne, E. M. Transdimensional approximate Bayesian computation for inference on invasive species models with latent variables of unknown dimension. Comput. Stat. Data Anal. 86, 97–110 (2015).

    MathSciNet  MATH  Article  Google Scholar 

  22. 22.

    Frelich, L. E. et al. Side-swiped: ecological cascades emanating from earthworm invasions. Front. Ecol. Environ. 17, 502–510 (2019).

    PubMed  PubMed Central  Article  Google Scholar 

  23. 23.

    Pauchard, A. et al. Non-native and native organisms moving into high elevation and high latitude ecosystems in an era of climate change: new challenges for ecology and conservation. Biol. Invasions 18, 345–353 (2016).

    Article  Google Scholar 

  24. 24.

    Nicolsky, D. J., Romanovsky, V. E., Panda, S. K., Marchenko, S. S. & Muskett, R. R. Applicability of the ecosystem type approach to model permafrost dynamics across the Alaska North Slope. J. Geophys. Res. 122, 50–75 (2017).

    Article  Google Scholar 

  25. 25.

    Phillips, H. R. P. et al. Global distribution of earthworm diversity. Science 366, 480–485 (2019).

    ADS  CAS  PubMed  Article  Google Scholar 

  26. 26.

    Craven, D. et al. The unseen invaders: introduced earthworms as drivers of change in plant communities in North American forests (a meta-analysis). Glob. Change Biol. 23, 1065–1074 (2017).

    ADS  Article  Google Scholar 

  27. 27.

    Wackett, A. A., Yoo, K., Olofsson, J. & Klaminder, J. Human-mediated introduction of geoengineering earthworms in the Fennoscandian arctic. Biol. Invasions 20, 1377–1386 (2018).

    Article  Google Scholar 

  28. 28.

    Haimi, J. & Huhta, V. Effects of earthworms on decomposition processes in raw humus forest soil—a microcosm study. Biol. Fertil. Soils 10, 178–183 (1990).

    Google Scholar 

  29. 29.

    Eskelinen, A., Stark, S. & Männistö, M. Links between plant community composition, soil organic matter quality and microbial communities in contrasting tundra habitats. Oecologia 161, 113–123 (2009).

    ADS  PubMed  Article  Google Scholar 

  30. 30.

    Bjork, R. G. et al. Linkages between N turnover and plant community structure in a tundra landscape. Plant Soil 294, 247–261 (2007).

    Article  CAS  Google Scholar 

  31. 31.

    Cameron, E. K., Cahill, J. F. & Bayne, E. M. Root foraging influences plant growth responses to earthworm foraging. PLoS One 9, 6 (2014).

    Google Scholar 

  32. 32.

    Chapin, F. S. & Shaver, G. R. Individualistic growth-response of tundra plant-species to environmental manipulations in the field. Ecology 66, 564–576 (1985).

    Article  Google Scholar 

  33. 33.

    Schwieger, S., Kreyling, J., Milbau, A. & Blume-Werry, G. Autumnal warming does not change root phenology in two contrasting vegetation types of subarctic tundra. Plant Soil 424, 145–156 (2018).

    CAS  Article  Google Scholar 

  34. 34.

    Blume-Werry, G. et al. Proportion of fine roots, but not plant biomass allocation below ground, increases with elevation in arctic tundra. J. Veg. Sci. 29, 226–235 (2018).

    Article  Google Scholar 

  35. 35.

    Kaarlejarvi, E. et al. Effects of warming on shrub abundance and chemistry drive ecosystem-level changes in a forest-tundra ecotone. Ecosystems 15, 1219–1233 (2012).

    Article  CAS  Google Scholar 

  36. 36.

    Sundqvist, M. K., Giesler, R. & Wardle, D. A. Within- and across-species responses of plant traits and litter decomposition to elevation across contrasting vegetation types in subarctic tundra. PLoS ONE 6, 12 (2011).

    Article  CAS  Google Scholar 

  37. 37.

    Barthelemy, H., Stark, S. & Olofsson, J. Strong responses of subarctic plant communities to long-term reindeer feces manipulation. Ecosystems 18, 740–751 (2015).

    CAS  Article  Google Scholar 

  38. 38.

    Bjorkman, A. D. et al. Plant functional trait change across a warming tundra biome. Nature 562, 57 (2018). +.

    ADS  CAS  PubMed  Article  Google Scholar 

  39. 39.

    Jia, G. J., Epstein, H. E. & Walker, D. A. Greening of arctic Alaska, 1981–2001. Geophys. Res. Lett. (2003).

    Article  Google Scholar 

  40. 40.

    Verbyla, D. The greening and browning of Alaska based on 1982–2003 satellite data. Glob. Ecol. Biogeogr. 17, 547–555 (2008).

    Article  Google Scholar 

  41. 41.

    Van Groenigen, J. W. et al. How fertile are earthworm casts? A meta-analysis. Geoderma 338, 525–535 (2019).

    ADS  Article  CAS  Google Scholar 

  42. 42.

    Darwin, C. Vegetable Mould and Earthworms. (John Murray, 1881).

  43. 43.

    Barthelemy, H., Stark, S., Michelsen, A. & Olofsson, J. Urine is an important nitrogen source for plants irrespective of vegetation composition in an Arctic tundra: Insights from a N-15-enriched urea tracer experiment. J. Ecol. 106, 367–378 (2018).

    CAS  Article  Google Scholar 

  44. 44.

    Stark, S. & Vaisanen, M. Insensitivity of soil microbial activity to temporal variation in soil n in subarctic tundra: evidence from responses to large migratory grazers. Ecosystems 17, 906–917 (2014).

    Article  Google Scholar 

  45. 45.

    Barthelemy, H., Dorrepaal, E. & Olofsson, J. Defoliation of a grass is mediated by the positive effect of dung deposition, moss removal and enhanced soil nutrient contents: results from a reindeer grazing simulation experiment. Oikos 128, 1515–1524 (2019).

    Article  Google Scholar 

  46. 46.

    Blume-Werry, G., Milbau, A., Teuber, L. M., Johansson, M. & Dorrepaal, E. Dwelling in the deep – strongly increased root growth and rooting depth enhance plant interactions with thawing permafrost soil. New Phytol. 223, 1328–1339 (2019).

    CAS  PubMed  Article  Google Scholar 

  47. 47.

    Booysen, M., Sikes, D., Bowser, M. L. & Andrews, R. Earthworms (Oligochaeta: Lumbricidae) of Interior Alaska. Biodiver. Data J. 6, 13 (2018).

    Article  Google Scholar 

  48. 48.

    Saltmarsh, D. M. et al. Distribution and abundance of exotic earthworms within a boreal forest system in southcentral Alaska. NeoBiota (2016).

    Article  Google Scholar 

  49. 49.

    Tiunov, A. V., Hale, C. M., Holdsworth, A. R. & Vsevolodova-Perel, T. S. Invasion patterns of Lumbricidae into the previously earthworm-free areas of northeastern Europe and the western Great Lakes region of North America. Biol. Invasions 8, 1223–1234 (2006).

    Article  Google Scholar 

  50. 50.

    Godhall, D. W. Some consideration in the use of point quadrats for the analysis of vegetation. Aust. J. Sci. Res. B 5, 1–41 (1952).

    Article  Google Scholar 

  51. 51.

    nlme: Linear and Nonlinear Mixed Effects Models v. R package Version 3.1-141. (2019).

  52. 52.

    Shekhovtsov, S. V., Golovanova, E. V. & Peltek, S. E. Different dispersal histories of lineages of the earthworm Aporrectodea caliginosa (Lumbricidae, Annelida) in the Palearctic. Biol. Invasions 18, 751–761 (2016).

    Article  Google Scholar 

  53. 53.

    Reynolds, J. W. A contribution to our knowledge of the earthworm fauna of Newfoundland and Labrador, Canada (Oligochaeta, Lumbricidae). Megadrilogica 8, 5–8 (2000).

    Google Scholar 

  54. 54.

    Reynolds, J. W. Additional earthworms (Oligochaeta: Lumbricidae) from Colorado, USA. Megadrilogica 10, 29–37 (2004).

    Google Scholar 

  55. 55.

    Zenkova, I. V. & Rapoport, I. B. in Advances in Earthworm Taxonomy Vol. Advances in Earthworm Taxonomy VI (Annelida: Oligochaeta). 6th International Oligochaeta Taxonomy Meeting, Palmeira de Faro (Portugal) (ed Kasparek, M.) 141–151 (Taylor & Francis, 2013).

  56. 56.

    Gates, G. E. Burmese earthworms. An introduction to the systematics and biology of megadrile oligochaetes with special reference to southeast Asia. Trans. Am. Philos. Soc. 62, 0–326 (1972).

    Article  Google Scholar 

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We thank Lapplandstiftelsen, Swedish Research Council (2017-04548), FORMAS (2018-01301 and 2013-00533), Göran Gustafssons Stiftelse för natur och miljö i Lappland, the Gunnar och Ruth Björkmans fond för norrländsk botanisk forskning, and Oscar och Lilly Lammstiftelse for financial support. We thank Dr. Ann Milbau for her input during construction of the mesocosms. Plant drying and grinding was conducted in the laboratory facilities of Finnish Natural Resources Institute, Rovaniemi. We thank Alisa Brandt, Manuel Görich, Anna Ley, Laurenz Teuber, and Veronika Vikuk for practical help, and the Abisko Scientific Research Station for support. Open access funding provided by Umea University.

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G.B.W. designed, initiated, and maintained the experiment. G.B.W., E.K., J.O., M.S., M.V., and J.K. conducted the fieldwork statistical analyses was done by J.O. J.K. wrote the paper in collaboration with G.B.W., E.K., J.O., M.S., and M.V.

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Correspondence to Jonatan Klaminder.

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Blume-Werry, G., Krab, E.J., Olofsson, J. et al. Invasive earthworms unlock arctic plant nitrogen limitation. Nat Commun 11, 1766 (2020).

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