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Selected AbstractsOn the climate and weather of mountain and sub-arctic lakes in Europe and their susceptibility to future climate changeFRESHWATER BIOLOGY, Issue 12 2009R. THOMPSON Summary 1.,The complex terrain and heterogeneous nature of the mountain environment coupled with remoteness from major centres of human activity makes mountains challenging locations for meteorological investigations. Mountainous areas tend to have more varied and more extreme weather than lowlands. 2.,The EMERGE program has the primary aim of assessing the status of remote mountain and sub-arctic lakes throughout Europe for the first time. In this study, we describe the main features of the climate, ice-cover durations and recent temperature trends of these areas. The main weather characteristics of European mountain and sub-arctic lakes are their cold temperatures and year-round precipitation. Mean annual temperatures are generally close to 0 °C, and maximum summer temperatures reasonably close to 10 °C. 3.,Maritime versus continental settings determine the main differences in annual-temperature range among lake districts (10.5 °C in Scotland to 26.7 °C in Northern Finland), and a similar factor for ice-cover duration. Radiation ranges from low (120 W m,2) in the high latitude sub-arctic and high (237 W m,2) in the southern ranges of the Pyrenees and Rila. Similarly, precipitation is high in the main Alpine chain (250 cm year,1 in the Central Southern Alps) and low in the continental sub-arctic (65 cm year,1 in Northern Finland). 4.,The main temporal patterns in air temperature follow those of the adjacent lowlands. All the lake districts warmed during the last century. Spring temperature trends were highest in Finland; summer trends were weak everywhere; autumn trends were strongest in the west, in the Pyrenees and western Alps; while winter trends varied markedly, being high in the Pyrenees and Alps, low in Scotland and Norway and negative in Finland. 5.,Two new, limnological case studies on Lake Redon, in the Pyrenees, highlight the sensitivity of remote lakes to projected changes in the global climate. These two case studies involve close linkages between extreme chemical-precipitation events and synoptic wind-patterns, and between thermocline behaviour and features of the large-scale circulation. 6.,Individual lakes can be ultra-responsive to climate change. Even modest changes in future air temperatures will lead to major changes in lake temperatures and ice-cover duration and hence probably affect their ecological status. [source] Effects of the past and the present on species distribution: land-use history and demography of wintergreenJOURNAL OF ECOLOGY, Issue 2 2000Kathleen Donohue Summary 1,Past land use can have long-term effects on plant species' distributional patterns if alterations in resources and environmental conditions have persistent effects on population demography (environmental change) and/or if plants are intrinsically limited in their colonization ability (historical factors). 2,We evaluated the role of environmental alteration vs. historical factors in controlling distributional patterns of Gaultheria procumbens, a woody, clonal understorey species with a pronounced restriction to areas that have never been ploughed, and near absence from adjoining areas that were ploughed in the 19th century. The demographic study was conducted in scrub oak and hardwood plant communities on an extensive sand plain, where it was possible to control for the effect of variation in environment prior to land use. 3,The observed demographic effects were contrary to the hypothesis that persistent environmental alteration depressed demographic performance and limited the distribution of G. procumbens. We observed no overall effect of land-use history on stem density, stem recruitment or flower production. In fact, some aspects of performance were enhanced in previously ploughed areas. Populations in previously ploughed areas exhibited less stem mortality in scrub oak transitions, an increase in germination, seedling longevity and proportion of potentially reproductive stems in both plant communities, a trend for slower observed rates of population decline in both plant communities, and a higher projected rate of population growth in the scrub oak transitions. Thus, particularly in scrub oak communities, the lower abundance of G. procumbens in formerly ploughed than in unploughed areas contrasted with its performance. 4,The limited occurrence of G. procumbens in formerly farmed areas was explained instead by its slow intrinsic growth rate, coupled with limited seedling establishment. Lateral population extension occurred exclusively through vegetative growth, allowing a maximum expansion of 43 cm year,1. 5,We conclude that inherent limitations in the colonizing ability of some plant species may present a major obstacle in the restoration or recovery of plant communities on intensively disturbed sites, even in the absence of persistent environmental effects that depress population growth. [source] Prey consumption rates and growth of piscivorous brown trout in a subarctic watercourseJOURNAL OF FISH BIOLOGY, Issue 3 2006H. Jensen Prey consumption rates of piscivorous brown trout Salmo trutta were studied in the Pasvik watercourse, which forms the border between Norway and Russia. Estimates of food consumption in the field were similar to or slightly less than maximum values from a bioenergetic model. The piscivore diet consisted mainly of vendace Coregonus albula with a smaller number of whitefish Coregonus lavaretus. Individual brown trout had an estimated mean daily intake of c. 1·5 vendace and 0·4 whitefish, and a rapid annual growth increment of 7,8 cm year,1. The total population of brown trout >25 cm total length was estimated as 8445 individuals (0·6 individuals ha,1), giving a mean ± s.e. annual consumption of 1553880 ± 405360 vendace and 439140 ± 287130 whitefish for the whole watercourse. The rapid growth in summer of brown trout >25 cm indicated a high prey consumption rate. [source] Modelling the relationship between sexual reproduction and rhizome growth in Posidonia oceanica (L.) DelileMARINE ECOLOGY, Issue 4 2006Sebastiano Calvo Abstract The relationship between flowering and growth performance of Posidonia oceanica (L.) Delile in meadows distributed along the south-eastern coast of Sicily (Italy) was investigated by means of a statistical model (generalized linear mixed model) combined with the lepidochronological analysis. Over a 28-year period, 67 floral stalk remains were observed. The highest flowering index was recorded in lepidochronological year 1998 (10.1%) and the Inflorescence Frequency per age showed a clear decrease corresponding to 15-year-old shoots. The sexual reproductive event had positive effects on rhizome elongation (cm year,1) and leaf production (no. leaves year,1) in the same flowering year, whilst no effect on the rhizome production (mg year,1) was observed. Rhizome growth variables showed significant negative lagged responses in the two years following flowering. On the whole, we calculated that the effect exerted by flowering, in terms of loss on rhizome elongation and production, was about 27% and 38%, respectively. Although it has been demonstrated that recovery from the stress induced by sexual reproduction is limited to the two years after flowering, the magnitude of the reproductive cost may become quite considerable especially in comparison with the whole lifespan of individual shoots. [source] | ||||||||||