Terry V. Callaghan

Plant community responses to experimental warming across the tundra biome

Recent observations of changes in some tundra ecosystems appear to be responses to a warming climate. Several experimental studies have shown that tundra plants and ecosystems can respond strongly to environmental change, including warming; however, most studies were limited to a single location and were of short duration and based on a variety of experimental designs. In addition, comparisons among studies are difficult because a variety of techniques have been used to achieve experimental warming and different measurements have been used to assess responses. We used metaanalysis on plant community measurements from standardized warming experiments at 11 locations across the tundra biome involved in the International Tundra Experiment. The passive warming treatment increased plant-level air temperature by 1-3°C, which is in the range of predicted and observed warming for tundra regions. Responses were rapid and detected in whole plant communities after only two growing seasons. Overall, warming increased height and cover of deciduous shrubs and graminoids, decreased cover of mosses and lichens, and decreased species diversity and evenness. These results predict that warming will cause a decline in biodiversity across a wide variety of tundra, at least in the short term. They also provide rigorous experimental evidence that recently observed increases in shrub cover in many tundra regions are in response to climate warming. These changes have important implications for processes and interactions within tundra ecosystems and between tundra and the atmosphere.

Ecological Dynamics Across the Arctic Associated with Recent Climate Change

Assessing the Arctic The Arctic is experiencing some of the most rapid climate change currently under way across the globe, but consequent ecological responses have not been widely reported. At the close of the Fourth International Polar Year, Post et al. (p. 1355) review observations on ecological impacts in this sensitive region. The widespread changes occurring in terrestrial, freshwater, and marine systems, presage changes at lower latitudes that will affect natural resources, food production, and future climate buffering. At the close of the Fourth International Polar Year, we take stock of the ecological consequences of recent climate change in the Arctic, focusing on effects at population, community, and ecosystem scales. Despite the buffering effect of landscape heterogeneity, Arctic ecosystems and the trophic relationships that structure them have been severely perturbed. These rapid changes may be a bellwether of changes to come at lower latitudes and have the potential to affect ecosystem services related to natural resources, food production, climate regulation, and cultural integrity. We highlight areas of ecological research that deserve priority as the Arctic continues to warm.

The Balance between Positive and Negative Plant Interactions and Its Relationship to Environmental Gradients: A Model

Positive, beneficial interactions between individuals within plant communities have been observed in nature and recorded in a wide variety of ecological experiments. However, the existence of such interactions has been, and continues to be, largely ignored by most ecological researchers. We present here a new model that combines current ecological theory on plant competition, and its relationship to environmental severity, with evidence from a range of studies that show positive plant interactions in the field. The model describes a hypothetical relationship between the intensity of positive (e.g. mutualistic) and negative (e.g. competitive) interactions between members of a plant community, and the severity of the external environment. It also provides an explanation for the past and current neglect of positive plant interactions, and for the conflicting results from plant community manipulation experiments examining such phenomena. Potential directions for future research into positive plant interactions are proposed.

Microbial biomass C, N and P in two arctic soils and responses to addition of NPK fertilizer and sugar: implications for plant nutrient uptake

The soil microbial carbon (C), nitrogen (N) and phosphorus (P) pools were quantified in the organic horizon of soils from an arctic/alpine low-altitude heath and a high-altitude fellfield by the fumigation-extraction method before and after factorial addition of sugar, NPK fertilizer and benomyl, a fungicide. In unamended soil, microbial C, N and P made up 3.3–3.6%, 6.1–7.3% and 34.7% of the total soil C, N and P content, respectively. The inorganic extractable N pool was below 0.1% and the inorganic extractable P content slightly less than 1% of the total soil pool sizes. Benomyl addition in spring and summer did not affect microbial C or nutrient content analysed in the autumn. Sugar amendments increased microbial C by 15 and 37% in the two soils, respectively, but did not affect the microbial nutrient content, whereas inorganic N and P either declined significantly or tended to decline. The increased microbial C indicates that the microbial biomass also increased but without a proportional enhancement of N and P uptake. NPK addition did not affect the amount of microbial C but almost doubled the microbial N pool and more than doubled the P pool. A separate study has shown that CO2 evolution increased by more than 50% after sugar amendment and by about 30% after NPK and NK additions to one of the soils. Hence, the microbial biomass did not increase in response to NPK addition, but the microbes immobilized large amounts of the added nutrients and, judging by the increased CO2 evolution, their activity increased. We conclude: (1) that microbial biomass production in these soils is stimulated by labile carbon and that the microbial activity is stimulated by both labile C and by nutrients (N); (2) that the microbial biomass is a strong sink for nutrients and that the microbial community probably can withdraw substantial amounts of nutrients from the inorganic, plant-available pool, at least periodically; (3) that temporary declines in microbial populations are likely to release a flush of inorganic nutrients to the soil, particularly P of which the microbial biomass contained more than one third of the total soil pool; and (4) that the mobilization-immobilization cycles of nutrients coupled to the population dynamics of soil organisms can be a significant regulating factor for the nutrient supply to the primary producers, which are usually strongly nutrient-limited in arctic ecosystems.

Temperature and vegetation seasonality diminishment over northern lands

Pronounced increases in winter temperature result in lower seasonal temperature differences, with implications for vegetation seasonality and productivity. Research now indicates that temperature and vegetation seasonality in northern ecosystems have diminished to an extent equivalent to a southerly shift of 4°– 7° in latitude, and may reach the equivalent of up to 20° over the twenty-first century.

Comparative responses of phenology and reproductive development to simulated environmental change in sub-Arctic and high Arctic plants

The effects of temperature, precipitation and nutrient perturbations, and their interactions, are being assessed on two contrasting arctic ecosystems to simulate impacts of climate change. One, a high arctic polar semi-desert community, is characterised by a sparse, low and aggregated vegetation cover where plant proliferation is by seedlings, whereas the other, a sub-arctic dwarf shrub heath, is characterised by a complete vegetation cover of erect, clonal dwarf shrubs which spread vegetatively. The developmental processes of seed production were shown to be highly sensitive, even within one growing season, to specific environmental perturbations which differed between sites

Positive Plant Interactions in Tundra Vegetation and the Importance of Shelter

The hypothesis that positive plant interactions, arising from species aggregations, are important in harsh environments was tested on the sedge Carex bigelowii in the alpine/subarctic tundra of Swedish Lapland. Association analyses showhed that, in contrast to records for the High Arctic, aggregations of the low-growing species ( 2 cm away from the dwarf shrubs or outside the moss mat (...)

Growth responses of four sub-Arctic dwarf shrubs to simulated environmental change

Vegetative responses of Empetrum hermaphroditum, Vaccinium vitis-idaea, V. uliginosum and V. myrtillus to environmental change (temperature (T), water (W) and fertilizer (F)) were investigated in a factorial field perturbation study in sub-Arctic Sweden over two growing seasons (1991 and 1992). Total above-ground biomass was largely unresponsive to the perturbations due to dilution of current seasons growth by material produced in previous years. The mass of shoot material produced in 1991, increased in response to F within 11 weeks of the start of the experiment in the two evergreen species (V. vitis-idaea and E. hermaphroditum), but not in the only deciduous species (V. uliginosum) measured that year (...)

Global Change and the Boreal Forest: Thresholds, Shifting States or Gradual Change?

Abstract Changes in boreal climate of the magnitude projected for the 21st century have always caused vegetation changes large enough to be societally important. However, the rates and patterns of vegetation change are difficult to predict. We review evidence suggesting that these vegetation changes may be gradual at the northern forest limit or where seed dispersal limits species distribution. However, forest composition may be quite resilient to climate change in the central portions of a species range until some threshold is surpassed. At this point, changes can be rapid and unexpected, often causing a switch to very different ecosystem types. Many of these triggers for change are amenable to management, suggesting that our choice of policies in the coming decades will substantially influence the ecological and societal consequences of current climatic change.

In situ mineralization of nitorgen and phosphorus of arctic soils after perturbations simulating climate change

Seasonal net nitrogen (N) and phosphorus (P) mineralization was investigated at Abisko, Swedish Lapland in soils of a subarctic heath and in soils of a colder (by about 4° C), high altitude fellfield by (a) using in situ soil incubation in soils which had been shaded or subjected to two levels of increased temperature, combined with (b) reciprocal transplantation of soils between the two sites. Proportionally large and significant net seasonal mineralization of N, in contrast to non-significant P mineralization, was found in untransplanted and transplanted fellfield soil. In contrast, P was mineralized in proportionally large amounts, in contrast to low N mineralization, in the transplanted and untransplanted heath soil. The differences indicate that P was strongly immobilized in relation to N at the fellfield and that N was more strongly immobilized than P in the heath soil. The immobilization in both soils remained high even after a temperature change of 4–5° C experienced by transplanted soils. Air temperature increases of up to 4–5° C in greenhouses resulted in a soil temperature increase of 1–2° C and did not cause any extra increase of net N and P mineralization. The results suggest that soil temperature increases of up to 2° C, which are likely to occur by the end of the next century as an effect of a predicted 4–5° C rise in air temperature, have only small effects on net mineralization in at least two characteristic tundra soils. These effects are probably smaller than the natural fluctuation of plant available nutrients from site to site, even within the same plant community. A further soil temperature increase of up to 4–5° C may enhance decomposition and gross mineralization, but the rate of net mineralization, and hence the change of nutrient availability to the plants, depends on the extent of microbial immobilization of the extra nutrients released.