Northern forest ecosystems are exposed to a range of anthropogenic processes including global warming, atmospheric deposition, and changing land-use. The vegetation of northern forests is composed of species with several functional traits related to these processes, whose effects may be difficult to disentangle. Here, we combined analyses of spatio-temporal dynamics and functional traits of ground flora species, including morphological characteristics, responses to macro- and microclimate, soil conditions, and disturbance. Based on data from the Swedish National Forest Inventory, we compared changes in occurrence of a large number of ground flora species during a 20-year period (1994-2013) in boreal and temperate Sweden respectively. Our results show that a majority of the common ground flora species have changed their overall frequency. Comparisons of functional traits between increasing and declining species, and of trends in mean trait values of sample plots, indicate that current floristic changes are caused by combined effects of climate warming, nitrogen deposition and changing land-use. Changes and their relations with plant traits were generally larger in temperate southern Sweden. Nutrient-demanding species with mesotrophic morphology were favored by ongoing eutrophication due to nitrogen deposition in the temperate zone, while dwarf shrubs with low demands on nitrogen decreased in frequency. An increase of species with less northern and less eastern distribution limits was also restricted to temperate Sweden, and indicates effects of a moister and milder macroclimate. A trend toward dense plantation forests is mirrored by a decrease of light-demanding species in both vegetation zones, and a decrease of grassland species in the temperate zone. Although denser tree canopies may buffer effects of a warmer climate and of nitrogen deposition to some extent, traits related to these processes were weakly correlated in the group of species with changing frequency. Hence, our results indicate specific effects of these often confounded anthropogenic processes.
Questions Does the influence of forest edges on plant species richness and composition depend on forest management? Do forest specialists and generalists show contrasting patterns? Location Mesic, deciduous forests across Europe. Methods Vegetation surveys were performed in forests with three management types (unthinned, thinned 5–10 years ago and recently thinned) along a macroclimatic gradient from Italy to Norway. In each of 45 forests, we established five vegetation plots along a south‐facing edge‐to‐interior gradient (n = 225). Forest specialist, generalist and total species richness, as well as evenness and proportion of specialists, were tested as a function of the management type and distance to the edge while accounting for several environmental variables (e.g. landscape composition and soil characteristics). Magnitude and distance of edge influence were estimated for species richness per management type. Results Greatest total species richness was found in thinned forests. Edge influence on generalist plant species richness was contingent on the management type, with the smallest decrease in species richness from the edge‐to‐interior in unthinned forests. In addition, generalist richness increased with the proportion of forests in the surrounding landscape and decreased in forests dominated by tree species that cast more shade. Forest specialist species richness, however, was not affected by management type or distance to the edge, and only increased with pH and increasing proportion of forests in the landscape. Conclusions Forest thinning affects the plant community composition along edge‐to‐interior transects of European forests, with richness of forest specialists and generalists responding differently. Therefore, future studies should take the forest management into account when interpreting edge‐to‐interior because both modify the microclimate, soil processes and deposition of polluting aerosols. This interaction is key to predict the effects of global change on forest plants in landscapes characterized by the mosaic of forest patches and agricultural land that is typical for Europe.
Question Does the abundance of keystone forest floor species change in response to changes in the forest structure? Location Sweden Methods We used data from the Swedish National Forest Inventory to investigate changes in the abundance of three common species, as well as the total abundance of all understorey vascular plants (the field layer) in forests in the boreal and temperate parts of Sweden. GLMs and GAMs were used to relate species abundance and temporal changes in abundances to forest structure and forest structural change. Results Productivity, measured as the site index, was the most important determinant of individual species' abundance. The volume of Picea abies, the density of tree stems and forest age were among the most important forest structural variables. We found that the dwarf shrub Vaccinium myrtillus, the narrow‐leaved grasses (mainly Avenella flexuosa) and the total field layer cover decreased in boreal Sweden from 1994 through 2010 and that these changes coincided with an increase in forest density and with a reduction in forest age. Conclusions Changes in Swedish forests to higher tree layer density and younger age appear to contribute significantly to current changes in forest floor vegetation. The use of more intensive thinning practices to reduce the total density of the forest and to increase the proportion of broad‐leaved tree species and Pinus sylvestris would favour the forest floor species in this study. Moreover, increasing forest age (i.e. the length of rotation periods) might favour V. myrtillus in particular, for which the time since disturbance is important for the recovery of pre‐disturbance abundance. However, increased thinning intensity and forest age will reduce the potential for wood production, implying a trade‐off between production of wood and maintenance of well‐developed forest floor vegetation.
The nutrient balancing hypothesis proposes that, when sufficient food is available, the primary goal of animal diet selection is to obtain a nutritionally balanced diet. This hypothesis can be tested using the Geometric Framework for nutrition (GF). The GF enables researchers to study patterns of nutrient intake (e.g. macronutrients; protein, carbohydrates, fat), interactions between the different nutrients, and how an animal resolves the potential conflict between over-eating one or more nutrients and under-eating others during periods of dietary imbalance. Using the moose (Alces alces L.), a model species in the development of herbivore foraging theory, we conducted a feeding experiment guided by the GF, combining continuous observations of six captive moose with analysis of the macronutritional composition of foods. We identified the moose’s self-selected macronutrient target by allowing them to compose a diet by mixing two nutritionally complementary pellet types plus limited access to Salix browse. Such periods of free choice were intermixed with periods when they were restricted to one of the two pellet types plus Salix browse. Our observations of food intake by moose given free choice lend support to the nutrient balancing hypothesis, as the moose combined the foods in specific proportions that provided a particular ratio and amount of macronutrients. When restricted to either of two diets comprising a single pellet type, the moose i) maintained a relatively stable intake of non-protein energy while allowing protein intakes to vary with food composition, and ii) increased their intake of the food item that most closely resembled the self-selected macronutrient intake from the free choice periods, namely Salix browse. We place our results in the context of the nutritional strategy of the moose, ruminant physiology and the categorization of food quality.
Forest edges are interfaces between forest interiors and adjacent land cover types. They are important elements in the landscape with almost 20 % of the global forest area located within 100 m of the edge.Edges are structurally different from forest interiors, which results in unique edge influences on microclimate, functioning and biodiversity. These edge influences have been studied for multiple decades, yet there is only limited information available on how forest edge structure varies at the continental scale, and which factors drive this potential structural diversity. Here we quantified the structural variation along 45 edge-to-interior transects situated along latitudinal, elevational and management gradients across Europe. We combined state-of-the-art terrestrial laser scanning and conventional forest inventory techniques to investigate how the forest edge structure (e.g. plant area index, stem density, canopy height and foliage height diversity) varies and which factors affect this forest edge structural variability. Macroclimate, management, distance to the forest edge and tree community composition all influenced the forest edge structural variability and interestingly we detected interactive effects of our predictors as well. We found more abrupt edge-to-interior gradients (i.e. steeper slopes) in the plant area index in regularly thinned forests. In addition, latitude, mean annual temperature and humidity all affected edge-to-interior gradients in stem density. We also detected a simultaneous impact of both humidity and management, and humidity and distance to the forest edge, on the canopy height and foliage height diversity. These results contribute to our understanding of how environmental conditions and management shape the forest edge structure. Our findings stress the need for site-specific recommendations on forest edge management instead of generalized recommendations as the macroclimate substantially influences the forest edge structure.Only then, the forest edge microclimate, functioning and biodiversity can be conserved at a local scale.
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