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We report an exceptionally fast grassland recovery process from a karst plateau in SW Slovenia. Vegetation of old fields with different ages was sampled using a chronosequence of fields abandoned 1, 3, 6, 9, 13, 15 and 100 years ago. We prepared dendrogram dividing the data set into 9 clusters that were further analyzed: diagnostic species, ecological conditions and life forms were evaluated. The initial stage of succession was characterized by segetal weeds and indicated high levels of soil nutrients. The second stage was dominated by dense patches of perennial forbs (most of them ruderal species) preferring also high levels of soil nutrients. The third stage was dominated by caespitose hemicryptophyte grasses, many of them of sub-Mediterranean origin. The first two stages took 13 years and both could be considered as early successional stages developing on nutrient rich soils. These stages were switched to late successional stage characterized by seminatural grassland species. The quick succession can probably be attributed to the rich species pool of natural grassland flora, the small size and annual mowing of abandoned agricultural fields and the close proximity of seed sources. [ABSTRACT FROM AUTHOR]

Aims: The relative importance of species within an ecosystem shows spatio‐temporal variability related to both the terrain features and numerous rapidly changing factors. Accordingly, functional and species patterns may show some level of persistence, or, due to various disturbances, fluctuations. Communities with high species richness were found to maintain a higher degree of stability than species‐poor or perturbed vegetations; however, diversity and its stability may be spatio‐temporally variable. Based on these considerations, our aim was to assess the responses of a sandy pasture, both species‐wise and at the community level, to the relatively invariant habitat, and to the more rapidly changing environmental conditions. Location: Hungary. Methods: We surveyed the vegetation in an area of about 1 ha by means of high‐resolution spatio‐temporal sampling: we recorded the surface aerial cover (%) of the plant species during 15 campaigns covering spring, summer and autumn aspects for seven years (2013–2019) in 80 × 60 m grids. The biological activity of the ecosystem (above‐ground biomass, soil respiration) was also followed up together with the environmental limiting factors. Results: During the study period, which was characterized by significant warming, the grassland showed a balanced physiological performance with year‐to‐year variability. Fluctuating differentiation of the plant species with different environmental optima along with the terrain attributes was assumed to be responsible for this balanced physiological performance. Although community‐level diversity remained stable, some species favoring cooler, wetter positions disappeared. Conclusions: Terrain features of the study area within 1.5 m or less elevation differences created considerably heterogeneous conditions for a high number (114) of plant species with different ecological needs to co‐occur. The stability of the diversity was found to show terrain relatedness, that is spatial as well as temporal patterns compared to the null model of spatio‐temporal independence, and the ecosystem functions followed these patterns. [ABSTRACT FROM AUTHOR]

The European temperate forest zone has great importance, in terms of maintaining the habitats of not only forests but also anthropogenous grasslands, which were formed as a result of habitat reconstruction. These habitats have great importance, by means of nature conservation, landscape use, economy, and forest and grassland use. The mosaic-like habitat complexes that consist of these grasslands and forest patches help to increase biodiversity and supply the habitat for forest game. In this survey, changes in the vegetation of the temperate forests (Fagetum) of the Mátra Mountains of Hungary were investigated after reconstruction. In 2012, shrub cutting was carried out in the area of Parádóhuta, and then three different management methods (abandoning, mowing, and grazing) were utilized. Our goals were the following: to perform a vegetation survey of the sample areas (i); surveying the natural regeneration of the grassland and analyzing its biodiversity, nature conservation, and economical value (ii); and analyzing the vegetation in terms of nature conservation and valuing its life form spectrum, economy values, and livestock-feeding ability (iii). According to our results, systematic mowing and a less-intensive grazing had a significantly positive effect on biodiversity and the coverage of species, thus increasing the naturalness of the studied grassland habitats, while wild game were able to act as ecological engineers. [ABSTRACT FROM AUTHOR]

Aims: Ecological theories predict that assembly processes shape communities so that co-existing species may either be functionally more dissimilar ("divergence") or more similar ("convergence") than expected by chance. Two important factors that are rarely considered in combination are spatial scale and successional stage. Our aim is to identify different functional patterns during succession across spatial scales and to discuss the likely underlying assembly processes. We expect to find convergence due to environmental filtering at early succession, especially at the largest scales, and a tendency towards divergence driven by competitive interactions as succession unfolds and at smaller spatial scales. Location: Protected Landscape Area “Bohemian Karst”, Czech Republic. Methods: We studied three succession stages (two, eight and 55 years after abandonment). Each field was sampled using 40 1-m² quadrats containing 100 pins in a regular grid. We analysed trait dispersion at several combinations of grain and extent and characterised trait similarity using phylogeny and four traits: specific leaf area, leaf dry matter content, height, and seed mass analysed individually and combined using Gower distance (multi-trait dissimilarity). Results: In the youngest field, three of the traits individually and the multi-trait dissimilarity showed convergence regardless of scale. Phylogeny showed convergence at most spatial scales of the youngest stage. The other two fields showed greater divergence predominantly in the oldest field at the smallest spatial scale. Conclusions: The results are mainly congruent with theoretical expectations and provide a valuable example of directional changes from trait convergence to divergence along succession. The scale-invariant convergence in the early stages of succession seems to be the result of environmental filtering and weaker competitive exclusion. At later stages and particularly at smaller scales, divergence becomes more common, likely because competition limits the trait similarity of species. These results highlight the importance of predictable (non-random) changes in ecological succession. [ABSTRACT FROM AUTHOR]

Spatial patterns of ecosystem processes constitute significant sources of uncertainty in greenhouse gas flux estimations partly because the patterns are temporally dynamic. The aim of this study was to describe temporal variability in the spatial patterns of grassland CO2 and N2O flux under varying environmental conditions and to assess effects of the grassland management (grazing and mowing) on flux patterns. We made spatially explicit measurements of variables including soil respiration, aboveground biomass, N2O flux, soil water content, and soil temperature during a 4-year study in the vegetation periods at grazed and mowed grasslands. Sampling was conducted in 80 × 60 m grids of 10 m resolution with 78 sampling points in both study plots. Soil respiration was monitored nine times, and N2O flux was monitored twice during the study period. Altitude, soil organic carbon, and total soil nitrogen were used as background factors at each sampling position, while aboveground biomass, soil water content, and soil temperature were considered as covariates in the spatial analysis. Data were analyzed using variography and kriging. Altitude was autocorrelated over distances of 40–50 m in both plots and influenced spatial patterns of soil organic carbon, total soil nitrogen, and the covariates. Altitude was inversely related to soil water content and aboveground biomass and positively related to soil temperature. Autocorrelation lengths for soil respiration were similar on both plots (about 30 m), whereas autocorrelation lengths of N2O flux differed between plots (39 m in the grazed plot vs. 18 m in the mowed plot). Grazing appeared to increase heterogeneity and linkage of the spatial patterns, whereas mowing had a homogenizing effect. Spatial patterns of soil water content, soil respiration, and aboveground biomass were temporally variable especially in the first 2 years of the experiment, whereas spatial patterns were more persistent (mostly significant correlation at p < 0.05 between location ranks) in the second 2 years, following a wet year. Increased persistence of spatial patterns after a wet year indicated the recovery potential of grasslands following drought and suggested that adequate water supply could have a homogenizing effect on CO2 and N2O fluxes. [ABSTRACT FROM AUTHOR]

In this study eight temperate grassland sites were monitored for soil CO 2 efflux (R s ) and the spatial covariate soil water content (SWC) and soil temperature (T s ) at fine scale in over 77 measurement campaigns. The goals of this multisite study were to explore the correlations between environmental gradients and spatial patterns of R s , SWC and T s , which are not site-specific and to quantify the relevance of biotic and abiotic controls over spatial patterns along increasing vegetation structural complexity. These patterns in water-limited ecosystems in East-Central Europe are likely to be influenced by summer droughts caused by the changing climate. A consistent experimental setup was applied at the study sites including 75 sampling locations along 15 m circular transects. Spatial data processing was mainly based on variography. Two proxy variables were introduced to relate the site characteristics in terms of soils, water status and vegetation. Normalised SWC (SWCn) reconciled site-specific soil water regimes while normalised day of year integrated temperature and vegetation phenology. A principal component analysis revealed that the progressing closure of vegetation in combination with large R s and SWCn values, as well as low T s and R s variability support the detectability of spatial patterns found in both the abiotic and biotic variables. Our results showed that apart from SWC the pattern of soil temperature also had an effect on spatial structures. We detected that when the spatially structured variability of T s was low, a strong negative correlation existed between SWCn and the spatial autocorrelation length of R s with r = 0.66 (p < 0.001). However, for high spatially structured variability of T s , occurring presumably at low T s in spring and autumn, the correlation did not exist and it was difficult to quantify the spatial autocorrelation of R s . Our results are indicative of a potential shift from homogeneity and dominance of biotic processes to an increased heterogeneity and abiotic regulation in drought prone ecosystems under conditions of decreasing soil moisture. [ABSTRACT FROM AUTHOR]

Questions How does the spatial configuration of sampling units influence recorded plant species richness values at small spatial scales? What are the consequences of these findings for sampling methodology and rarefaction analyses? Location Six semi-natural grasslands in Western Eurasia (France, Germany, Bulgaria, Hungary, Italy, Turkey). Methods In each site we established six blocks of 40 cm × 280 cm, subdivided into 5 cm × 5 cm micro-quadrats, on which we recorded vascular plant species presence with the rooted (all sites) and shoot (four sites) presence method. Data of these micro-quadrats were then combined to achieve larger sampling units of 0.01, 0.04 and 0.16 m² grain size with six different spatial configurations (square, 4:1 rectangle, 16:1 rectangle, three variants of discontiguous randomly placed micro-quadrats). The effect of the spatial configurations on species richness was quantified as relative richness compared to the mean richness of the square of the same surface area. Results Square sampling units had significantly lower species richness than other spatial configurations in all countries. For 4:1 and 16:1 rectangles, the increase of rooted richness was on average about 2% and 8%, respectively. In contrast, the average richness increase for discontiguous configurations was 7%, 17% and 40%. In general, increases were higher with shoot presence than with rooted presence. Overall, the patterns of richness increase were highly consistent across six countries, three grain sizes and two recording methods. Conclusions Our findings suggest that the shape of sampling units has negligible effects on species richness values when the length-width ratio is up to 4:1, and the effects remain small even for more elongated contiguous configurations. In contrast, results from discontiguous sampling units are not directly comparable with those of contiguous sampling units, and are strongly confounded by spatial extent. This is particularly problematic for rarefaction studies where spatial extent is often not controlled for. We suggest that the concept of effective area is a useful tool to report effects of spatial configuration on richness values, and introduce species-extent relationships ( SERs) to describe richness increases of different spatial configurations of sampling units. [ABSTRACT FROM AUTHOR]

Questions (i) Which species dominate mid-successional old-fields in Hungary? How does the identity of these species relate to local (patch-scale) diversity and to the progress of succession? (ii) Which species have the strongest negative impact on diversity in spontaneous old-field succession and what generalizations are possible about traits of these species? (iii) Are these species dominant or subordinate components in mature target communities? (iv) Do native or alien species have stronger effects on the diversity and progress of succession? Location Abandoned agricultural fields (abandoned croplands, orchards and vineyards) at various locations throughout Hungary. Methods Vegetation patterns on 112 old-fields, in 25 sites varying in soil and climatic conditions, topography, landscape contexts and land-use histories were sampled. Most old-fields had appropriate seed sources in the immediate vicinity, i.e. natural or semi-natural grasslands (meadows steppes, closed and open sand steppes) as source and target habitats. Age of abandoned fields ranged from 1 to 69 yr, but most sites were between 15 and 60 yr. The cover of vascular plant species (%) was estimated in 2 × 2-m plots. Relationships between diversity, progress of succession (similarity to target communities) and identity of dominants were tested. Results A small portion of successional dominants (eight species) had strong negative impacts on diversity. These species belonged to Poaceae, Asteraceae and Fabaceae. Most of these species were wind-pollinated, and capable of lateral vegetative spread. Dominant species varied in size and had, on average, a low requirement for N but a high requirement for light. With one exception, Solidago gigantea, they were native to the Hungarian flora. Significant differences were found among the impact of successional dominants when dominant species were grouped according to their original role (dominants or subordinates) in natural communities. The overall effect of species identity was also significant. Bothriochloa ischaemum was identified as the species with the strongest negative effect on species diversity. Conclusions Our results suggest that mid-successional dominant species differ in their impact on diversity and progress of succession. Mid-successional plots dominated by alien species, or by native species that were originally subordinate in natural communities, regenerate less successfully and may temporarily arrest succession. Therefore, early colonization of native dominants should be enhanced with restoration measures. [ABSTRACT FROM AUTHOR]