Phenological observations of major plant growth forms and species in montane and Eriophorum vaginatum tussock tundra in central Alaska

The development stages of several tundra plant species were observed during the summers of 1977 and 1978 in different vegetation zones in a snow accumulation area and in tussock tundra. Leaf maturation and senescence tend towards synchrony regardless of the time of emergence from under the snow. Flowering stages are less synchronous and general than are the vegetation stages within a growth form.     

Environmental and vegetational variation across a snow accumulation area in montane tundra in central Alaska

Several environmental factors were measured in a transect across a snow accumulation area in order to indicate (1) possible controls of arctic vegetation patterns; (2) water, carbon, and nutrient budgets of different vegetation types; and (3) relationships of Eriophorum vaginatum tussock tundra to other vegetation types. The results indicate that the vegetation zones are largely associated with different levels of nitrogen and phosphorus availability rather than length of the snowfree season, water availability, and soil pH. Nitrogen uptake was highest in the forb-grass and lower deciduous shrub zones and lowest in the lichen-heath. Phosphorus uptake was highest in the lower deciduous shrub zone and lowest in the lichen-heath. On the basis of several floristic and environmental factors tussock tundra has the lowest affinities to the lower deciduous shrub zone.     

Rapid recovery of kohekohe (

Soil conditions, vegetation features and soil fauna were recorded in montane tall tussock grassland dominated by narrow- leaved snow tussock Chionochloa rigida ssp. rigida up to 30 months after a spring fire. Burning reduced the stature of tussocks and the size and density of tillers in the first growing season. After two growing seasons, tussock canopy development and tiller size remained below those found in the unburnt grassland nearby. New tillers and tussocks established following the prolific fire-induced flowering one year after burning. After the fire and sheep grazing, intertussock cover became progressively dominated by introduced grasses and herbs. While soil pH, moisture content, bulk density, surface litter and total nematodes showed significant treatment (burning) effects, these properties also showed significant year-to-year variation. The greatest increase in any nematode group was in Paratylenchus, a distinctive genus widespread in tussock grasslands and apparently responsive to environmental fluctuation and root development; its population was 100x and 29x greater in the burned area than in the control area 16 and 30 months after burning. Subject to detailed testing, populations of mites and collembola may provide relatively simple indicators of recovery of ecosystem function of such grasslands after burning.     

Bacterial and fungal community structure in Arctic tundra tussock and shrub soils

Fungal and bacterial community structure in tussock, intertussock and shrub organic and mineral soils at Toolik Lake, Alaska were evaluated. Community structure was examined by constructing clone libraries of partial 16S and 18S rRNA genes. The soil communities were sampled at the end of the growing season in August 2004 and just after the soils thawed in June 2005. The communities differed greatly between vegetation types, although tussock and intertussock soil communities were very similar at the phyla level. The communities were relatively stable between sample dates at the phyla and subphyla levels, but differed significantly at finer phylogenetic scales. Tussock and intertussock bacterial communities were dominated by Acidobacteria, while shrub soils were dominated by Proteobacteria. These results appear consistent with previous work demonstrating that shrub soils contain an active, bioavailable C fraction, while tussock soils are dominated by more recalcitrant substrates. Tussock fungi communities had higher proportions of Ascomycota than shrub soils, while Zygomycota were more abundant in shrub soils. Recent documentation of increasing shrub abundance in the Arctic suggests that soil microbial communities and their functioning are likely to be altered by climate change.     

Factors determining plant species richness in Alaskan arctic tundra

Abstract. We studied the relationship between plant N:P ratio, soil characteristics and species richness in wet sedge and tussock tundra in northern Alaska at seven sites. We also collected data on soil characteristics, above‐ground biomass, species richness and composition. The N:P ratio of the vegetation did not show any relationship with species richness. The N:P ratio of the soil was related with species richness for both vegetation types. Species richness in the tussock tundra was most strongly correlated with soil calcium content and soil pH, with a strong correlation between these two factors. N:P ratio of the soil was also correlated with soil pH. Other factors correlated with species richness were soil moisture and Sphagnum cover. Organic matter content was the factor most strongly correlated with species richness in the wet sedge vegetation. N:P ratio of the soil was strongly correlated with organic matter content. We conclude that N:P ratio in the vegetation is not an important factor determining species richness in arctic tundra and that species richness in arctic tundra is mainly determined by pH and flooding. In tussock tundra the pH, declining with soil age, in combination with Sphagnum growth strongly decreases species richness, while in wet sedge communities flooding over long periods of time creates less favourable conditions for species richness.     

Leaf mineral nutrition of Arctic plants in response to warming and deeper snow in northern Alaska

Articulating the consequences of global climate change on terrestrial ecosystem biogeochemistry is a critical component of Arctic system studies. Leaf mineral nutrition responses of tundra plants is an important measure of changes in organismic and ecosystem attributes because leaf nitrogen and carbon contents effect photosynthesis, primary production, carbon budgets, leaf litter, and soil organic matter decomposition as well as herbivore forage quality. In this study, we used a longterm experiment where snow depth and summer temperatures were increased independently and together to articulate how a series of climate change scenarios would affect leaf N, leaf C, and leaf C:N for vegetation in dry and moist tussock tundra in northern Alaska, USA. Our findings were: 1) moist tundra vegetation is much more responsive to this suite of climate change scenarios than dry tundra with up to a 25% increase in leaf N; 2) life forms exhibit divergence in leaf C, N, and C:N with deciduous shrubs and graminoids having almost identical leaf N contents; 3) for some species, leaf mineral nutrition responses to these climate change scenarios are tundra type dependent ( Betula ), but for others ( Vaccinium vitis-idaea ), strong responses are exhibited regardless of tundra type; and 4) the seasonal patterns and magnitudes of leaf C and leaf N in deciduous and evergreen shrubs were responsive to conditions of deeper snow in winter. Leaf N is was generally higher immediately after emergence from the deep snow experimental treatments and leaf N was higher during the subsequent summer and fall, and the leaf C:N were lower, especially in deciduous shrubs. These findings indicate that coupled increases in snow depth and warmer summer temperatures will alter the magnitudes and patterns of leaf mineral nutrition and that the long term consequences of these changes may feed-forward and affect ecosystem processes.     

Effects of drainage and temperature on carbon balance of tussock tundra micrososms

We examined the importance of temperature (7°C or 15°C) and soil moisture regime (saturated or field capacity) on the carbon (C) balance of arctic tussock tundra microcosms (intact blocks of soil and vegetation) in growth chambers over an 81-day simulated growing season. We measured gaseous CO₂ exchanges, methane (CH₄) emissions, and dissolved C losses on intact blocks of tussock (Eriophorum vaginatum) and intertussock (moss-dominated). We hypothesized that under increased temperature and/or enhanced drainage, C losses from ecosystem respiration (CO₂ respired by plants and heterotrophs) would exceed gains from gross photosynthesis causing tussock tundra to become a net source of C to the atmosphere. The field capacity moisture regime caused a decrease in net CO₂ storage (NEP) in tussock tundra micrososms. This resulted from a stimulation of ecosystem respiration (probably mostly microbial) with enhanced drainage, rather than a decrease in gross photosynthesis. Elevated temperature alone had no effect on NEP because CO₂ losses from increased ecosystem respiration at elevated temperature were compensated by increased CO₂ uptake (gross photosynthesis). Although CO₂ losses from ecosystem respiration were primarily limited by drainage, CH₄ emissions, in contrast, were dependent on temperature. Furthermore, substantial dissolved C losses, especially organic C, and important microhabitat differences must be considered in estimating C balance for the tussock tundra system. As much as 20% of total C fixed in photosynthesis was lost as dissolved organic C. Tussocks stored 2x more C and emitted 5x more methane than intertussocks. In spite of the limitations of this microcosm experiment, this study has further elucidated the critical role of soil moisture regime and dissolved C losses in regulating net C balance of arctic tussock tundra.     

Interactions between Carbon and Nitrogen Mineralization and Soil Organic Matter Chemistry in Arctic Tundra Soils

We used long-term laboratory incubations and chemical fractionation to characterize the mineralization dynamics of organic soils from tussock, shrub, and wet meadow tundra communities, to determine the relationship between soil organic matter (SOM) decomposition and chemistry, and to quantify the relative proportions of carbon (C) and nitrogen (N) in tundra SOM that are biologically available for decomposition. In all soils but shrub, we found little decline in respiration rates over 1 year, although soils respired approximately a tenth to a third of total soil C. The lack of decline in respiration rates despite large C losses indicates that the quantity of organic matter available was not controlling respiration and thus suggests that something else was limiting microbial activity. To determine the nature of the respired C, we analyzed soil chemistry before and after the incubation using a peat fractionation scheme. Despite the large losses of soil C, SOM chemistry was relatively unchanged after the incubation. The decomposition dynamics we observed suggest that tundra SOM, which is largely plant detritus, fits within existing concepts of the litter decay continuum. The lack of changes in organic matter chemistry indicates that this material had already decomposed to the point where the breakdown of labile constituents was tied to lignin decomposition. N mineralization was correlated with C mineralization in our study, but shrub soil mineralized more and tussock soil less N than would have been predicted by this correlation. Our results suggest that a large proportion of tundra SOM is potentially mineralizable, despite the fact that decomposition was dependent on lignin breakdown, and that the historical accumulation of organic matter in tundra soils is the result of field conditions unfavorable to decomposition and not the result of fundamental chemical limitations to decomposition. Our study also suggests that the anticipated increases in shrub dominance may substantially alter the dynamics of SOM decomposition in the tundra. Received 31 January 2002; accepted 16 July 2002.     

Soil aeration in relation to soil physical properties, nitrogen availability, and root characteristics within an arctic watershed

The seasonal change in soil oxygen availability was determined in several habitats along a topographic moisture gradient in an arctic watershed. The effect of changes in soil aeration on soil chemical and plant properties was examined by comparison of the driest (tussocks) and wettest (wet sedge tundra) sites along this gradient. Spatial variability and seasonal change in soil oxygen availability was closely linked to the hydrologic regime and the thickness of the organic soil horizon. The greatest extension of the aerobic soil layer was found beneath well-drained tussocks, while less than 10% of the unfrozen soil layer is aerated in flooded wet sedge tundra. Intertussock areas and watertracks (channels of water drainage) have intermediate levels of aeration. In tussock tundra, soil oxygen diffusion is restricted in the mineral soil layer below the organic horizon due to reduced pore space. Organic matter constituents and their change with depth were similar beneath tussocks and in wet sedge tundra, indicating that factors other than soil aeration (e.g. low soil temperatures, short growing season) are the primary controls on decomposition in these two arctic tundra systems. NH₄ ⁺, the dominant form of inorganic N, was more available in wet sedge tundra than in tussock tundra. At both sites, extractable and soil solution NO₃ ^- concentrations increased 4 to 8 fold in the second part of the growing season, indicating increased nitrifier activity with improved soil oxygen availability. Although soils thawed as deep as 60 cm, approx. 90% of the root biomass was concentrated within 20 cm of the surface. Despite the anaerobic soil environment in wet sedge tundra, the dominant species there, Eriophorum angustifolium, reached slightly greater rooting depths than E. vaginatum, whose roots grow in the elevated, aerobic portion of tussocks. E. angustifolium had a root porosity of 31%, within the range found for wetland species, while roots of E. vaginatum had a porosity close to 12%. Rhizome porosity were low in both species (11%).     

Seasonal variation in enzyme activities and temperature sensitivities in Arctic tundra soils

Arctic soils contain large amounts of organic matter due to very slow rates of detritus decomposition. The first step in decomposition results from the activity of extracellular enzymes produced by soil microbes. We hypothesized that potential enzyme activities are low relative to the large stocks of organic matter in Arctic tundra soils, and that enzyme activity is low at in situ temperatures. We measured the potential activity of six hydrolytic enzymes at 4 and 20 °C on four sampling dates in tussock, intertussock, shrub organic, and shrub mineral soils at Toolik Lake, Alaska. Potential activities of N‐acetyl glucosaminidase, β‐glucosidase, and peptidase tended to be greatest at the end of winter, suggesting that microbes produced enzymes while soils were frozen. In general, enzyme activities did not increase during the Arctic summer, suggesting that enzyme production is N‐limited during the period when temperatures would otherwise drive higher enzyme activity in situ. We also detected seasonal variations in the temperature sensitivity (Q₁₀) of soil enzymes. In general, soil enzyme pools were more sensitive to temperature at the end of the winter than during the summer. We modeled potential in situβ‐glucosidase activities for tussock and shrub organic soils based on measured enzyme activities, temperature sensitivities, and daily soil temperature data. Modeled in situ enzyme activity in tussock soils increased briefly during the spring, then declined through the summer. In shrub soils, modeled enzyme activities increased through the spring thaw into early August, and then declined through the late summer and into winter. Overall, temperature is the strongest factor driving low in situ enzyme activities in the Arctic. However, enzyme activity was low during the summer, possibly due to N‐limitation of enzyme production, which would constrain enzyme activity during the brief period when temperatures would otherwise drive higher rates of decomposition.     

Changes in vegetation states in grazed and ungrazed Mackenzie Basin grasslands, New Zealand, 1990-2000

Changes in vegetation from 1990 to 2000 were examined at 10 high country localities, representing four grassland types: fescue tussock (Festuca novae-zelandiae), snow tussock (Chionochloa rigida), red tussock (C. rubra), and silver tussock (Poa cita). At each locality, three treatments were established: ambient sheep+rabbit grazing, rabbit grazing only, and no grazing. The mutivariate methods of classification and ordination were used on individual-quadrat cover data to define vegetation states and to examine transitions between them over time. Vegetation states in quadrats already dominated by Hieracium pilosella(> 50% cover) in 1990 showed little change in species composition regardless of grassland type and grazing treatment. In fescue tussock grassland, H. pilosellaincreased regardless of grazing treatment in states with low initial H. pilosellacover (< 5%), while the cover of Carex colensoi, Aira caryophyllea and Rumex acetosella decreased. In the single silver tussock locality, Poa citadecreased markedly in the ungrazed treatment as adventive species such as Dactylis glomerataand Echium vulgare increased. However, Poa citaalso decreased, probably due to drought, in the grazed treatment. Snow tussock and red tussock grassland states were more stable than those in short tussock grasslands, but there was also a general trend towards increasing H. pilosellacover in intertussock vegetation regardless of treatment. However, at one snow tussock locality, transitions from H. piloselladominated to C. rigida-dominated states occurred in ungrazed quadrats, while the reverse occurred in grazed vegetation. Implications for the management of tussock grasslands for conservation are discussed.     

Fine root production and nutrient content in wet and moist arctic tundras as influenced by chronic fertilization

We used ingrowth cores to estimate fine root production in organic soils of wet sedge and moist tundra ecosystems near Toolik Lake on Alaska's North Slope. Root-free soil cores contained in nylon mesh tubes (5 cm diameter, 20–30 cm long) were placed in control and chronically fertilized (N plus P) plots in mid-August 1994 and were retrieved 1 year later. Estimated fine root production in control plots was 75 g m^–2 year^–1 in wet sedge and 56 g m^–2 year^–1 in moist tussock tundra. Fine root production in fertilized plots was 85 g m^–2 year^–1 in wet sedge and 67 g m^–2 year^–1 in moist tussock tundra. Although our estimates of fine root production were higher on fertilized than control plots, differences were not statistically significant within either tundra type. Comparisons between our estimates of fine root production and other estimates of aboveground (plus rhizome) production on the same (wet sedge tundra) or similar (moist tussock tundra) plots suggest that fine root production was about one-third of total net primary production (NPP) under non-fertilized conditions and about one-fifth of total NPP under chronic fertilization. Fine root N and P concentrations increased with fertilization in both tundra types, but P concentrations increased more than N concentrations in wet sedge tundra, whereas relative increases in N and P concentrations in moist tundra roots were similar. These data are consistent with other studies suggesting that NPP in wet sedge tundra is often P limited and that co-limitation by N and P is more important in moist tussock tundra.     

Phosphorus Availability Determines the Response of Tundra Ecosystem Carbon Stocks to Nitrogen Enrichment

Northern permafrost soils contain important carbon stocks. Here we report the long-term response of carbon stocks in high Arctic dwarf shrub tundra to short-term, low-level nutrient enrichment. Twenty years after experimental nitrogen addition, carbon stocks in vegetation and organic soil had almost halved. In contrast, where phosphorus was added with nitrogen, carbon storage increased by more than 50%. These responses were explained by changes in the depths of the moss and organic soil layers. Nitrogen apparently stimulated decomposition, reducing carbon stocks, whilst phosphorus and nitrogen co-stimulated moss productivity, increasing organic matter accumulation. The altered structure of moss and soil layers changed soil thermal regimes, which may further influence decomposition of soil carbon. If climate warming increases phosphorus availability, any increases in nitrogen enrichment from soil warming or expanding human activity in the Arctic may result in increased carbon sequestration. Where phosphorus is limiting in tundra areas, however, nitrogen enrichment may result in carbon loss.     

Decomposition of old organic matter as a result of deeper active layers in a snow depth manipulation experiment

A snow addition experiment in moist acidic tussock tundra at Toolik Lake, Alaska, increased winter snow depths 2–3 m, and resulted in a doubling of the summer active layer depth. We used radiocarbon (?¹⁴C) to (1) determine the age of C respired in the deep soils under control and deepened active layer conditions (deep snow drifts), and (2) to determine the impact of increased snow and permafrost thawing on surface CO₂ efflux by partitioning respiration into autotrophic and heterotrophic components. ?¹⁴C signatures of surface respiration were higher in the deep snow areas, reflecting a decrease in the proportion of autotrophic respiration. The radiocarbon age of soil pore CO₂ sampled near the maximum mid-July thaw depth was approximately 1,000 years in deep snow treatment plots (45–55 cm thaw depth), while CO₂ from the ambient snow areas was ~100 years old (30-cm thaw depth). Heterotrophic respiration ?¹⁴C signatures from incubations were similar between the two snow depths for the organic horizon and were extremely variable in the mineral horizon, resulting in no significant differences between treatments in either month. Radiocarbon ages of heterotrophically respired C ranged from <50 to 235 years BP in July mineral soil samples and from 1,525 to 8,300 years BP in August samples, suggesting that old soil C in permafrost soils may be metabolized upon thawing. In the surface fluxes, this old C signal is obscured by the organic horizon fluxes, which are significantly higher. Our results indicate that, as permafrost in tussock tundra ecosystems of arctic Alaska thaws, carbon buried up to several thousands of years ago will become an active component of the carbon cycle, potentially accelerating the rise of CO₂ in the atmosphere.     

Nutrient Addition Prompts Rapid Destabilization of Organic Matter in an Arctic Tundra Ecosystem

Nutrient availability in the arctic is expected to increase in the next century due to accelerated decomposition associated with warming and, to a lesser extent, increased nitrogen deposition. To explore how changes in nutrient availability affect ecosystem carbon (C) cycling, we used radiocarbon to quantify changes in belowground C dynamics associated with long-term fertilization of graminoid-dominated tussock tundra at Toolik Lake, Alaska. Since 1981, yearly fertilization with nitrogen (N) and phosphorus (P) has resulted in a shift to shrub-dominated vegetation. These combined changes have altered the quantity and quality of litter inputs, the vertical distribution and dynamics of fine roots, and the decomposition rate of soil organic C. The loss of C from the deep organic and mineral soil has more than offset the C accumulation in the litter and upper organic soil horizons. In the litter and upper organic horizons, radiocarbon measurements show that increased inputs resulted in overall C accumulation, despite being offset by increased decomposition in some soil pools. To reconcile radiocarbon observations in the deeper organic and mineral soil layers, where most of the ecosystem C loss occurred, both a decrease in input of new root material and a dramatic increase of decomposition rates in centuries-old soil C pools were required. Therefore, with future increases in nutrient availability, we may expect substantial losses of C which took centuries to accumulate.     

Carex sempervirens tussocks induce spatial heterogeneity in litter decomposition, but not in soil properties, in a subalpine grassland in the Central Alps

Tussocks of graminoids can induce spatial heterogeneity in soil properties in dry areas with discontinuous vegetation cover, but little is known about the situation in areas with continuous vegetation and no study has tested whether tussocks can induce spatial heterogeneity in litter decomposition. In a subalpine grassland in the Central Alps where vegetation cover is continuous, we measured soil properties [concentration of N, C, organic matter (OM) and pH] and monitored litter decomposition traits (dry mass loss, loss of C, N, P and K) inside and outside tussocks of Carex sempervirens. Soil C, N, OM concentrations or pH inside tussocks did not differ significantly from those outside tussocks. After 1 year of decomposition, litter dry mass loss, C and K loss were significantly smaller inside than outside tussocks. The slower litter decomposition inside tussocks was likely caused by the elevated tussock base, which made environmental conditions inside tussocks much dryer than those outside in early spring when snow melts. Our results suggest that in areas with continuous vegetation cover tussocks induce spatial heterogeneity in litter decomposition but not in soil properties.     

Denitrification Potential, Root Biomass, and Organic Matter in Degraded and Restored Urban Riparian Zones

Hydrologic changes associated with urbanization often lead to lower water tables and drier, more aerobic soils in riparian zones. These changes reduce the potential for denitrification, an anaerobic microbial process that converts nitrate, a common water pollutant, into nitrogen gas. In addition to oxygen, denitrification is controlled by soil organic matter and nitrate. Geomorphic stream restorations are common in urban areas, but their effects on riparian soil conditions and denitrification have not been evaluated. We measured root biomass, soil organic matter, and denitrification potential (anaerobic slurry assay) at four depths in duplicate degraded, restored, and reference riparian zones in the Baltimore, Maryland, U.S.A., metropolitan area. There were three main findings in this study. First, although reference sites were wet and had high soil organic matter, they had low levels of nitrate relative to degraded and restored sites and therefore there were few differences in denitrification potential among sites. Evaluations of riparian restorations that have nitrate removal by denitrification as a goal should consider the complex controls of this process and how they vary between sites. Second, all variables declined markedly with depth in the soil. Restorations that increase riparian water tables will thus foster interaction of groundwater nitrate with near-surface soils with higher denitrification potential. Third, we observed strong positive relationships between root biomass and soil organic matter and between soil organic matter and denitrification potential, which suggest that establishment of deep-rooted vegetation may be particularly important for increasing the depth of the active denitrification zone in restored riparian zones.     

Production and export of dissolved C in arctic tundra mesocosms: the roles of vegetation and water flow

To better understand carbon (C) cycling in arctic tundra we measureddissolved C production and export rates in mesocosms of three tundra vegetationtypes: tussock, inter-tussock and wet sedge. Three flushing frequencies wereused to simulate storm events and determine potential mass export of dissolved Cunder increased soil water flow scenarios. Dissolved C production and exportrates differed between vegetation types (inter-tussock < tussock < wetsedge). In the absence of flushing, dissolved organic C (DOC) dominatedproduction in tussock and inter-tussock soils but was consumed in wet sedgesoils (8.3, 32.7, and –0.4 g C g soil^–1day^–1). Soil water dissolved C concentrations declined over time when flushedat high and medium frequencies but were variable at low flushing frequency.Total yield of dissolved C and DOC increased with increased flushing frequency.The ratio of DOC to dissolved inorganic C exported dropped with increasedflushing under tussock but not inter-tussock or wet sedge vegetation. Massexport per liter of water added declined as flushing frequency increased intussock and inter-tussock mesocosms. Export and production of dissolved C werestrongly correlated with above ground biomass, but not with photosynthetic ratesor below ground biomass. DOC quality was examined by measuring production ofToolik Lake bacteria fed mesocosm soil water. When normalized for DOCconcentration, wet sedge soil water supported significantly higher bacterialproduction. Our results indicate that arctic tundra soils have high potentialsfor dissolved C export, that water flow and vegetation type mainly controldissolved C export, and that responses of aquatic microbes to terrestrial inputsdepend on the vegetation type in the watershed.     

Winter regulation of tundra litter carbon and nitrogen dynamics

Mass and nitrogen (N) dynamics of leaf litter measured in Alaskan tussock tundra differed greatly from measurements of these processes made in temperate ecosystems. Nearly all litter mass and N loss occurred during the winter when soils were mostly frozen. Litter lost mass during the first summer, but during the subsequent two summers when biological activity was presumably higher than it is during winter, litter mass remained constant and litter immobilized N. By contrast, litter lost significant mass and N over both winters of measurement. Mass loss and N dynamics were unaffected by microsite variation in soil temperature and moisture. Whether wintertime mass and N loss resulted from biological activity during winter or from physical processes (e.g., fragmentation or leaching) associated with freeze-thaw is unknown, but has implications for how future climate warming will alter carbon (C) and N cycling in tundra. We hypothesize that spring runoff over permafrost as soils melt results in significant losses of C and N from litter, consistent with the observed influx of terrestrial organic matter to tundra lakes and streams after snow melt and the strong N limitation of terrestrial primary production.     

The nature of spatial transitions in the Arctic

Aim Describe the spatial and temporal properties of transitions in the Arctic and develop a conceptual understanding of the nature of these spatial transitions in the face of directional environmental change. Location Arctic tundra ecosystems of the North Slope of Alaska and the tundra‐forest region of the Seward Peninsula, Alaska Methods We synthesize information from numerous studies on tundra and treeline ecosystems in an effort to document the spatial changes that occur across four arctic transitions. These transitions are: (i) the transition between High‐Arctic and Low‐Arctic systems, (ii) the transition between moist non‐acidic tundra (MNT) and moist acidic tundra (MAT, also referred to as tussock tundra), (iii) the transition between tussock tundra and shrub tundra, (iv) the transition between tundra and forested systems. By documenting the nature of these spatial transitions, in terms of their environmental controls and vegetation patterns, we develop a conceptual model of temporal dynamics of arctic ecotones in response to environmental change. Results Our observations suggest that each transition is sensitive to a unique combination of controlling factors. The transition between High and Low Arctic is sensitive primarily to climate, whereas the MNT/MAT transition is also controlled by soil parent material, permafrost and hydrology. The tussock/shrub tundra transition appears to be responsive to several factors, including climate, topography and hydrology. Finally, the tundra/forest boundary responds primarily to climate and to climatically associated changes in permafrost. There were also important differences in the demography and distribution of the dominant plant species across the four vegetation transitions. The shrubs that characterize the tussock/shrub transition can achieve dominance potentially within a decade, whereas spruce trees often require several decades to centuries to achieve dominance within tundra, and Sphagnum moss colonization of non‐acidic sites at the MNT/MAT boundary may require centuries to millennia of soil development. Main conclusions We suggest that vegetation will respond most rapidly to climatic change when (i) the vegetation transition correlates more strongly with climate than with other environmental variables, (ii) dominant species exhibit gradual changes in abundance across spatial transitions, and/or (iii) the dominant species have demographic properties that allow rapid increases in abundance following climatic shifts. All three of these properties characterize the transition between tussock tundra and low shrub tundra. It is therefore not surprising that of the four transitions studied this is the one that appears to be responding most rapidly to climatic warming.