Elisabeth J. Cooper
University of Tromsø
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Featured researches published by Elisabeth J. Cooper.
Nature Climate Change | 2012
Sarah C. Elmendorf; Gregory H. R. Henry; Robert D. Hollister; Robert G. Björk; Noémie Boulanger-Lapointe; Elisabeth J. Cooper; Johannes H. C. Cornelissen; Thomas A. Day; Ellen Dorrepaal; Tatiana G. Elumeeva; Mike Gill; William A. Gould; John Harte; David S. Hik; Annika Hofgaard; David R. Johnson; Jill F. Johnstone; Ingibjörg S. Jónsdóttir; Janet C. Jorgenson; Kari Klanderud; Julia A. Klein; Saewan Koh; Gaku Kudo; Mark Lara; Esther Lévesque; Borgthor Magnusson; Jeremy L. May; Joel A. Mercado-Díaz; Anders Michelsen; Ulf Molau
Temperature is increasing at unprecedented rates across most of the tundra biome(1). Remote-sensing data indicate that contemporary climate warming has already resulted in increased productivity ov ...
Polar Research | 2010
Elke Morgner; Bo Elberling; Ditte Strebel; Elisabeth J. Cooper
Winter respiration in snow-covered ecosystems strongly influences annual carbon cycling, underlining the importance of processes related to the timing and quantity of snow. Fences were used to increase snow depth from 30 to 150 cm, and impacts on respiration were investigated in heath and mesic meadow, two common vegetation types in Svalbard. We manually measured ecosystem respiration from July 2007 to July 2008 at a temporal resolution greater than previously achieved in the High Arctic (campaigns: summer, eight; autumn, six; winter, 17; spring, nine). Moisture contents of unfrozen soil and soil temperatures throughout the year were also recorded. The increased snow depth resulted in significantly higher winter soil temperatures and increased ecosystem respiration. A temperature–efflux model explained most of the variation of observed effluxes: meadows, 94 (controls) and 93% (fences); heaths, 84 and 77%, respectively. Snow fences increased the total non-growing season efflux from 70 to 92 (heaths) and from 68 to 125 g CO2-C m-2 (meadows). The non-growing season contributed to 56 (heaths) and 42% (meadows) of the total annual carbon respired. This proportion increased with deeper snow to 64% in both vegetation types. Summer respiration rates were unaffected by snow fences, but the total growing season respiration was lower behind fences because of the considerably delayed snowmelt. Meadows had higher summer respiration rates than heaths. In addition, non-steady state CO2 effluxes were measured as bursts lasting several days during spring soil thawing, and when ice layers were broken to carry out winter efflux measurements.
Journal of Vegetation Science | 2004
Elisabeth J. Cooper; Inger Greve Alsos; Dagmar Hagen; Fiona M. Smith; Stephen J. Coulson; Ian D. Hodkinson
Abstract Composition and density of the soil seed banks, together with seedling emergence in the field, were examined on Svalbard. 1213 soil samples were collected from six dry-mesic habitats in three regions representing various stages of colonization from bare moraines to full vegetation cover and spanning a range of typical nutrient and thermal regimes. Of the 165 vascular plant species native to Svalbard, 72 were present as mature plants at the study sites and of these 70% germinated seed. Proglacial soil had 12 seedlings per m2, disturbed Dryas heath 131, intact Dryas heath 91, polar heath 715, thermophilic heath 3113, and a bird cliff 10437 seedlings. Highest seed bank species richness was at the thermophilic heath (26 species). Seedlings of 27 species emerged in the field, with fewer seedlings in disturbed habitats (60 seedlings per m2) than in intact Dryas heath (142), suggesting that an absence of ‘safe sites’ limited seedling establishment in disturbed habitats. Measurement of seedling emergence in the field increased awareness of which species are able to germinate naturally. This may be underestimated by up to 31% if greenhouse trials alone are used, owing partly to unsuitability of greenhouse conditions for germination of some species and also to practical limitations of amount of soil sampled. Most thermophilic species failed to germinate and some species present at several sites only germinated from the thermophilic heath seed bank, suggesting that climate constrains recruitment from seeds in the High Arctic. Nomenclature: Elven & Elvebakk (1996).
Journal of Vegetation Science | 2001
René van der Wal; Rob W. Brooker; Elisabeth J. Cooper; Rolf Langvatn
We studied the effects of Svalbard reindeer on the abundance of lichens in Spitsbergen. A survey was carried out in 14 areas with contrasting reindeer densities. Separate cover estimates for crustose, fructose and foliose lichens were taken in each area, and related to the density of reindeer pellet groups, a measure of reindeer density. Dominant macrolichen families were identified in 10 areas, and a full record of macrolichen species was taken in four additional areas. Varia- tion in reindeer density is partially due to past overhunting, and subsequent incomplete recovery, releasing some areas from reindeer grazing for 100-200 yr. The cover of fruticose lichens was negatively related to reindeer pellet group density, indicating suppression by Svalbard reindeer. This makes their impact comparable to other members of the Rangifer genus around the northern hemisphere. The generally recorded low abundance of lichens in the diet of Svalbard reindeer compared to other Rangifer species, therefore, was interpreted as the depletion of fruticose lichens in Spitsbergen, and a subsequent switch to alternative foods. Of all fruticose lichens, Stereocaulon spp. appeared least sensitive to grazing. Crustose and foliose lichen cover was independent of reindeer pellet group density. The cover of crustose lichens was significantly related to latitude, with greater cover in more northern areas. Foliose lichens were more abundant in places where moss cover was high. We conclude that the impact of Svalbard reindeer on lichens is dependent on growth form, with fruticose lichens suffering from grazing, whereas foliose lichens might indirectly benefit from higher densities of reindeer or, like crustose lichens, be controlled by other factors.
Global Biogeochemical Cycles | 2010
Mats P. Björkman; Elke Morgner; Elisabeth J. Cooper; Bo Elberling; Leif Klemedtsson; Robert G. Björk
The winter CO(2) efflux from subnivean environments is an important component of annual C budgets in Arctic ecosystems and consequently makes prediction and estimations of winter processes as well ...
Ecology and Evolution | 2013
Philipp R. Semenchuk; Bo Elberling; Elisabeth J. Cooper
Abstract The High Arctic winter is expected to be altered through ongoing and future climate change. Winter precipitation and snow depth are projected to increase and melt out dates change accordingly. Also, snow cover and depth will play an important role in protecting plant canopy from increasingly more frequent extreme winter warming events. Flower production of many Arctic plants is dependent on melt out timing, since season length determines resource availability for flower preformation. We erected snow fences to increase snow depth and shorten growing season, and counted flowers of six species over 5 years, during which we experienced two extreme winter warming events. Most species were resistant to snow cover increase, but two species reduced flower abundance due to shortened growing seasons. Cassiope tetragona responded strongly with fewer flowers in deep snow regimes during years without extreme events, while Stellaria crassipes responded partly. Snow pack thickness determined whether winter warming events had an effect on flower abundance of some species. Warming events clearly reduced flower abundance in shallow but not in deep snow regimes of Cassiope tetragona, but only marginally for Dryas octopetala. However, the affected species were resilient and individuals did not experience any long term effects. In the case of short or cold summers, a subset of species suffered reduced reproductive success, which may affect future plant composition through possible cascading competition effects. Extreme winter warming events were shown to expose the canopy to cold winter air. The following summer most of the overwintering flower buds could not produce flowers. Thus reproductive success is reduced if this occurs in subsequent years. We conclude that snow depth influences flower abundance by altering season length and by protecting or exposing flower buds to cold winter air, but most species studied are resistant to changes. Winter warming events, often occurring together with rain, can substantially remove snow cover and thereby expose plants to cold winter air. Depending on morphology, different parts of the plant can be directly exposed. On this picture, we see Dryas octopetala seed heads from the previous growing season protrude through the remaining ice layer after a warming event in early 2010. The rest of the plant, including meristems and flower primordia, are still somewhat protected by the ice. In the background we can see a patch of Cassiope tetragona protruding through the ice; in this case, the whole plant including flower primordia is exposed, which might be one reason why this species experienced a loss of flowers the following season. Photograph by Philipp Semenchuk.
Biogeochemistry | 2015
Philipp R. Semenchuk; Bo Elberling; Cecilie Amtorp; Judith Winkler; Sabine B. Rumpf; Anders Michelsen; Elisabeth J. Cooper
Nitrogen (N) mineralization, nutrient availability, and plant growth in the Arctic are often restricted by low temperatures. Predicted increases of cold-season temperatures may be important for plant nutrient availability and growth, given that N mineralization is also taking place during the cold season. Changing nutrient availability may be reflected in plant N and chlorophyll content and lead to increased photosynthetic capacity, plant growth, and ultimately carbon (C) assimilation by plants. In this study, we increased snow depth and thereby cold-season soil temperatures in high Arctic Svalbard in two vegetation types spanning three moisture regimes. We measured growing-season availability of ammonium (NH4+), nitrate (NO3−), total dissolved organic carbon (DOC) and nitrogen (TON) in soil; C, N, δ15N and chlorophyll content in Salix polaris leaves; and leaf sizes of Salix, Bistorta vivipara, and Luzula arcuata at peak season. Nutrient availability was significantly higher with increased snow depth in the two mesic meadow vegetation types, but not in the drier heath vegetation. Nitrogen concentrations and δ15N values of Salix leaves were significantly higher in all vegetation types, but the leaf sizes were unchanged. Leaves of Bistorta and Luzula were significantly larger but only significantly so in one moist vegetation type. Increased N and chlorophyll concentrations in leaves indicate a potential for increased growth (C uptake), supported by large leaf sizes for some species. Responses to cold-season soil warming are vegetation type- and species-specific, with potentially stronger responses in moister vegetation types. This study therefore highlights the contrasting effect of snow in a tundra landscape and has important implications for projections of whole tundra responses to climate change.
Polar Research | 2010
Mats P. Björkman; Elke Morgner; Robert G. Björk; Elisabeth J. Cooper; Bo Elberling; Leif Klemedtsson
Recent climate change predictions suggest altered patterns of winter precipitation across the Arctic. It has been suggested that the presence, timing and quantity of snow all affect microbial activity, thus influencing CO2 production in soil. In this study annual and seasonal emissions of CO2 were estimated in High-Arctic Adventdalen, Svalbard, and sub-Arctic Latnjajaure, Sweden, using a new trace gas-based method to track real-time diffusion rates through the snow. Summer measurements from snow-free soils were made using a chamber-based method. Measurements were obtained from different snow regimes in order to evaluate the effect of snow depth on winter CO2 effluxes. Total annual emissions of CO2 from the sub-Arctic site (0.662-1.487 kg CO2 m-2 yr-1) were found to be more than double the emissions from the High-Arctic site (0.369-0.591 kg CO2 m-2 yr-1). There were no significant differences in winter effluxes between snow regimes or vegetation types, indicating that spatial variability in winter soil CO2 effluxes are not directly linked to snow cover thickness or soil temperatures. Total winter emissions (0.004- 0.248 kg CO2 m-2) were found to be in the lower range of those previously described in the literature. Winter emissions varied in their contribution to total annual production between 1 and 18%. Artificial snow drifts shortened the snow-free period by 2 weeks and decreased the annual CO2 emission by up to 20%. This study suggests that future shifts in vegetation zones may increase soil respiration from Arctic tundra regions.
Arctic, Antarctic, and Alpine Research | 2003
Elisabeth J. Cooper; Philip A. Wookey
Abstract In polar semidesert communities of northwest Spitsbergen the reproductive potential of keystone vascular plant species, such as Dryas octopetala, is currently being constrained by low summer temperatures, resulting in the infrequent production of viable seeds. This study tests the hypothesis that summer foraging behavior of reindeer (Rangifer tarandus platyrhynchus) may further limit successful seed production due to intense selective grazing pressure on the flowering shoots. Surveys of neighboring coastal tundra areas with contrasting reindeer population densities revealed direct evidence of strong grazing pressure on reproductive shoots of D. octopetala on the Brøgger Peninsula and considerably less floral herbivory on the sparsely reindeer-populated Blomstrand island. Recruitment of Dryas on the Brøgger Peninsula is therefore being hindered by intense selective grazing of flowering shoots by Svalbard reindeer. This situation is not unique to this area of Svalbard and also extends to other species of flowering plants.
PLOS ONE | 2014
Sabine B. Rumpf; Philipp R. Semenchuk; Stefan Dullinger; Elisabeth J. Cooper
The Arctic is one of the ecosystems most affected by climate change; in particular, winter temperatures and precipitation are predicted to increase with consequent changes to snow cover depth and duration. Whether the snow-free period will be shortened or prolonged depends on the extent and temporal patterns of the temperature and precipitation rise; resulting changes will likely affect plant growth with cascading effects throughout the ecosystem. We experimentally manipulated snow regimes using snow fences and shoveling and assessed aboveground size of eight common high arctic plant species weekly throughout the summer. We demonstrated that plant growth responded to snow regime, and that air temperature sum during the snow free period was the best predictor for plant size. The majority of our studied species showed periodic growth; increases in plant size stopped after certain cumulative temperatures were obtained. Plants in early snow-free treatments without additional spring warming were smaller than controls. Response to deeper snow with later melt-out varied between species and categorizing responses by growth forms or habitat associations did not reveal generic trends. We therefore stress the importance of examining responses at the species level, since generalized predictions of aboveground growth responses to changing snow regimes cannot be made.