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Grassland Vegetation (grassland + vegetation)
Selected AbstractsFlux and turnover of fixed carbon in soil microbial biomass of limed and unlimed plots of an upland grassland ecosystemENVIRONMENTAL MICROBIOLOGY, Issue 4 2005J. Ignacio Rangel-Castro Summary The influence of liming on rhizosphere microbial biomass C and incorporation of root exudates was studied in the field by in situ pulse labelling of temperate grassland vegetation with 13CO2 for a 3-day period. In plots that had been limed (CaCO3 amended) annually for 3 years, incorporation into shoots and roots was, respectively, greater and lower than in unlimed plots. Analysis of chloroform-labile C demonstrated lower levels of 13C incorporation into microbial biomass in limed soils compared to unlimed soils. The turnover of the recently assimilated 13C compounds was faster in microbial biomass from limed than that from unlimed soils, suggesting that liming increases incorporation by microbial communities of root exudates. An exponential decay model of 13C in total microbial biomass in limed soils indicated that the half-life of the tracer within this carbon pool was 4.7 days. Results are presented and discussed in relation to the absolute values of 13C fixed and allocated within the plant,soil system. [source] Signals of range expansions and contractions of vascular plants in the high Alps: observations (1994,2004) at the GLORIA, master site Schrankogel, Tyrol, AustriaGLOBAL CHANGE BIOLOGY, Issue 1 2007HARALD PAULI Abstract High mountain ecosystems are defined by low temperatures and are therefore considered to react sensitively to climate warming. Responding to observed changes in plant species richness on high peaks of the European Alps, an extensive setup of 1 m × 1 m permanent plots was established at the alpine-nival ecotone (between 2900 and 3450 m) on Mount Schrankogel, a GLORIA master site in the central Tyrolean Alps, Austria, in 1994. Recording was repeated in a representative selection of 362 quadrats in 2004. Ten years after the first recording, we observed an average change in vascular plant species richness from 11.4 to 12.7 species per plot, an increase of 11.8% (or of at least 10.6% at a 95% confidence level). The increase in species richness involved 23 species (about 43% of all taxa found at the ecotone), comprising both alpine and nival species and was pronouncedly higher in plots with subnival/nival vegetation than in plots with alpine grassland vegetation. Only three species showed a decrease in plot occupancy: one was an annual species, one was rare, and one a common nival plant that decreased in one part of the area but increased in the uppermost part. Species cover changed in relation to altitudinal preferences of species, showing significant declines of all subnival to nival plants, whereas alpine pioneer species increased in cover. Recent climate warming in the Alps, which has been twice as high as the global average, is considered to be the primary driver of the observed differential changes in species cover. Our results indicate an ongoing range contraction of subnival to nival species at their rear (i.e. lower) edge and a concurrent expansion of alpine pioneer species at their leading edge. Although this was expected from predictive distribution models and different temperature-related habitat preferences of alpine and nival species, we provide first evidence on , most likely , warming-induced species declines in the high European Alps. The projected acceleration of climate warming raises concerns that this phenomenon could become the major threat to biodiversity in high mountains. [source] Virus infection and grazing exert counteracting influences on survivorship of native bunchgrass seedlings competing with invasive exoticsJOURNAL OF ECOLOGY, Issue 2 2006C. M. MALMSTROM Summary 1,Invasive annual grasses introduced by European settlers have largely displaced native grassland vegetation in California and now form dense stands that constrain the establishment of native perennial bunchgrass seedlings. Bunchgrass seedlings face additional pressures from both livestock grazing and barley and cereal yellow dwarf viruses (B/CYDVs), which infect both young and established grasses throughout the state. 2,Previous work suggested that B/CYDVs could mediate apparent competition between invasive exotic grasses and native bunchgrasses in California. 3,To investigate the potential significance of virus-mediated mortality for early survivorship of bunchgrass seedlings, we compared the separate and combined effects of virus infection, competition and simulated grazing in a field experiment. We infected two species of young bunchgrasses that show different sensitivity to B/CYDV infection, subjected them to competition with three different densities of exotic annuals crossed with two clipping treatments, and monitored their growth and first-year survivorship. 4,Although virus infection alone did not reduce first-year survivorship, it halved the survivorship of bunchgrasses competing with exotics. Within an environment in which competition strongly reduces seedling survivorship (as in natural grasslands), virus infection therefore has the power to cause additional seedling mortality and alter patterns of establishment. 5,Surprisingly, clipping did not reduce bunchgrass survivorship further, but rather doubled it and disproportionately increased survivorship of infected bunchgrasses. 6,Together with previous work, these findings show that B/CYDVs can be potentially powerful elements influencing species interactions in natural grasslands. 7,More generally, our findings demonstrate the potential significance of multitrophic interactions in virus ecology. Although sometimes treated collectively as plant ,predators', viruses and herbivores may exert influences that are distinctly different, even counteracting. [source] A measure for spatial heterogeneity of a grassland vegetation based on the beta-binomial distributionJOURNAL OF VEGETATION SCIENCE, Issue 5 2000Masae Shiyomi Abstract. A method is proposed to estimate the frequency and the spatial heterogeneity of occurrence of individual plant species composing the community of a grassland or a plant community with a short height. The measure is based on the beta-binomial distribution. The weighted average heterogeneity of all the species composing a community provides a measure of community-level heterogeneity determining the spatial intricateness of community composition of existing species. As an example to illustrate the method, a sown grassland with grazing cows was analysed, on 102 quadrats of 50 cm × 50 cm, each of which divided into four small quadrats of 25 cm × 25 cm. The frequency of occurrence for all the species was recorded in each small quadrat. Good fits to the beta-binomial series for most species of the community were obtained. These results indicate that (1) each species is distributed heterogeneously with respective spatial patterns, (2) the degree of heterogeneity is different from species to species, and (3) the beta-binomial distribution can be applied for grassland communities. In most of the observed species spatial heterogeneity is often characterized by species-specific propagating traits: seed-propagating plant species exhibited a low heterogeneity/random pattern while clonal species exhibited a high heterogeneity/aggregated pattern. This measure can be applied to field surveys and to the estimation of community parameters for grassland diagnosis. [source] A comparative study of seed number, seed size, seedling size and recruitment in grassland plantsOIKOS, Issue 3 2000Anna Jakobsson In this study we analyse relationships between seed number, seed size, seedling size and recruitment success in grassland plants. The often hypothesised trade-off between seed size and seed number was supported by a cross-species analysis and by an analysis of 35 phylogenetically independent contrasts, derived from a data-set of 72 species. Apart from among-species relatedness, we also controlled for possible confounding effect of plant size that may influence both seed size and seed number. A sowing experiment with 50 species was performed in the field. The seeds were sown in a grassland and subjected to two treatments, disturbance and undisturbed sward. Evidence for seed-limited recruitment was obtained for 45 of the species. Disturbance had a significant, or nearly significant, positive effect on recruitment for 16 of the 45 species. The relative recruitment in undisturbed sward increased with increased seed size, and both recruitment success and seedling size were positively related to seed size. We suggest that a trade-off between competitive ability and number of recruitment opportunities follows from the trade-off between seed size and seed number, through a causal chain from seed size via seedling size to recruitment success. The relationships between seed size, seed number and recruitment may be an important underlying mechanism for abundance and dynamics of plant species in grassland vegetation. This is an example of a direct link between evolutionary life-history theory, and theory of plant community structure. [source] Inventorying management status and plant species richness in semi-natural grasslands using high spatial resolution imageryAPPLIED VEGETATION SCIENCE, Issue 2 2010K. Hall Abstract Question: Can we reliably estimate grazing intensity, indicators of grazing intensity (i.e. field-layer height and shrub-cover), and vascular plant species richness in semi-natural grasslands from high spatial resolution satellite data? Location: The Baltic Island of Öland (Sweden). Methods: Fieldwork included the on-site description of grazed and ungrazed areas and shrub-cover within 107 semi-natural grassland sites. Field-layer height and vascular plant species richness (total within-site and mean small-scale species richness) were recorded within the sites. Digital classification of QuickBird data was performed to identify grazed and ungrazed areas and shrub-cover. Vegetation indices were generated to analyze the performance of satellite data for estimating field-layer height, and the spectral heterogeneity was used to characterize the within-site environmental heterogeneity. Results: The proportion of digitally classified grazed area explained 45% of the variation in field-layer height and 43% of the variation in shrub-cover. Field-layer height was significantly related to vegetation indices. A linear model with three explanatory variables (spectral richnessred, spectral richnessNIR, and shrub-cover) explained 47% of the variation in total within-site species richness. Conclusions: High spatial resolution imagery may assist in the monitoring of the processes that follow the cessation of grazing, on the scale of individual grassland sites. Measures of spectral heterogeneity acquired by high spatial resolution imagery can be used in the assessment of total within-site vascular plant species richness in semi-natural grassland vegetation. [source] | |||||||||||||