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Plant Species Diversity (plant + species_diversity)
Selected AbstractsMacrophyte species diversity in formerly cultivated wetlands in UgandaAFRICAN JOURNAL OF ECOLOGY, Issue 4 2008Josephine Esaete Abstract The diversity of major macrophytes was assessed in cultivated areas in Bukasa and Kinawataka wetlands in Central Uganda. One thousand and seventy-two plots of 1 × 1 m were established in 69 cultivated areas. Data were collected on species richness and abundance. Two-way analysis of covariance (ANCOVA) showed how cropping regimes affected macrophyte species richness and abundance. There were 127 plant species belonging to 37 families in cultivated areas. Of the 127 species, 42 were macrophytes and of the 37 families, fourteen contained macrophyte species. Plant species diversity was higher in the short-term cropping regime areas (11.3 species per 1 m2) than in the long-term cropping regime areas (9.3 species per 1 m2). However, macrophyte species richness was similar in the short-term (3.2 species per 1 m2) and the long-term (3.3 species per 1 m2) cropping regimes. The dominant families were Poaceae, Asteraceae and Cyperaceae with more than ten species each. The higher plant species diversity in cultivated areas than in uncultivated was because of nonmacrophyte species, thus cropping regime does not influence macrophyte species diversity. Increase in diversity of nonmacrophyte species in short-term cropping regime implies that the use of wetlands for agricultural crop growing may alter plant species composition and diversity during secondary succession. Résumé La diversité des principaux macrophytes a étéévaluée dans les régions cultivées des zones humides de Bukasa et de Kinawataka, au centre de l'Ouganda. On a établi 1072 plots d'1x1m, dans 69 zones cultivées. On a récolté des données sur la richesse et l'abondance des espèces. Une analyse de la covariance à deux voies (ANCOVA) a montré comment les régimes agricoles affectaient la richesse et l'abondance des espèces de macrophytes. Il y avait 127 espèces végétales appartenant à 37 familles dans les zones cultivées. De ces 127 espèces, 42 étaient des macrophytes, et des 37 familles, 14 comprenaient des espèces de macrophytes. La diversité des espèces végétales était plus élevée dans les surfaces subissant un régime cultural court (11,3 espèces/m2) que dans les surfaces soumises à un régime de culture plus long (9,3 espèces/m2). Cependant, la richesse en espèces de macrophytes était comparable pour le régime court (3,2 espèces/m2) et pour le plus long (3,3 espèces/m2). Les familles dominantes étaient les Poaceae, les Asteraceae et les Cyperaceae, qui comptaient chacune plus de 10 espèces. La diversité spécifique plus grande observée dans les aires cultivées était due aux espèces non macrophytes, et on peut donc dire que le régime de culture n'influence pas la diversité des espèces de macrophytes. L'augmentation de la diversité des espèces non macrophytes dans les cultures à régime court implique que l'utilisation des zones humides pour l'agriculture peut altérer par la suite la composition et la diversité des espèces végétales. [source] Effect of Hydrologic Restoration and Lonicera maackii Removal on Herbaceous Understory Vegetation in a Bottomland Hardwood ForestRESTORATION ECOLOGY, Issue 3 2008Rebecca M. Swab Abstract Amur honeysuckle (Lonicera maackii (Rupr.) Herder), a large deciduous shrub from China, has invaded many forests in eastern/central United States. The species was removed by cutting and herbicide application from a recently hydrologically restored section of a bottomland hardwood forest in central Ohio, and the response of understory plants, especially herbaceous species, was measured. Plots were established in uncleared and cleared sections, and percent cover of each herbaceous understory species was estimated monthly. One season after several years of Lonicera removal efforts, no significant association was discovered between percentage of Lonicera cover and total understory species abundance. There was, however, a direct correlation between elevation and honeysuckle abundance; L. maackii abundance was negatively associated with low elevations, likely due to hydrologic factors. Plant species diversity (H) and richness (s) increased with elevation but were not significantly different on plots with honeysuckle removal (H = 0.86 ± 0.08 vs. 0.78 ± 0.09 and s = 4.4 ± 0.19 vs. 4.2 ± 0.2 species/m2, respectively) despite the fact that understory light levels measured by densiometer were significantly higher (,= 0.003) in cleared versus uncleared sections. Native and invasive species were found in similar proportions in the two sections, and significant sprouting and regrowth of L. maackii were observed throughout the cleared section. Although the removal of L. maackii altered the characteristics of the plant species assemblage, the value of this management remains questionable in the years immediately following treatment. [source] Acidification of sandy grasslands , consequences for plant diversityAPPLIED VEGETATION SCIENCE, Issue 3 2009Pål Axel Olsson Abstract Questions: (1) Does soil acidification in calcareous sandy grasslands lead to loss of plant diversity? (2) What is the relationship between the soil content of lime and the plant availability of mineral nitrogen (N) and phosphorus (P) in sandy grasslands? Location: Sandy glaciofluvial deposits in south-eastern Sweden covered by xeric sand calcareous grasslands (EU habitat directive 6120). Methods: Soil and vegetation were investigated in most of the xeric sand calcareous grasslands in the Scania region (136 sample plots distributed over four or five major areas and about 25 different sites). Environmental variables were recorded at each plot, and soil samples were analysed for exchangeable P and N, as well as limestone content and pH. Data were analysed with regression analysis and canonical correspondence analysis. Results: Plant species richness was highest on weakly acid to slightly alkaline soil; a number of nationally red-listed species showed a similar pattern. Plant species diversity and number of red-listed species increased with slope. Where the topsoil had been acidified, limestone was rarely present above a depth of 30 cm. The presence of limestone restricts the availability of soil P, placing a major constraint on primary productivity in sandy soils. Conclusions: Acidification of sandy grasslands leads to reduced abundance of desirable species, although the overall effect is rather weak between pH 5 and pH 9. Slopes are important for high diversity in sandy grasslands. Calcareous soils cannot be restored through shallow ploughing, but deep perturbation could increase the limestone content of the topsoil and favour of target species. [source] Investigating the evolution of floras: problems and progress , An introductionDIVERSITY AND DISTRIBUTIONS, Issue 1 2006H. P. Linder ABSTRACT The Cape flora of southern Africa is a remarkable hotspot for plant species diversity and endemism. At a meeting in Zurich in 2004 progress in understanding the evolution of this diversity was reviewed. In this symposium, four papers presenting several of the methods used in this investigation were reported. These papers deal with molecular dating methods, the reconstruction of ancestral habitats, with possible speciation scenarios for the Cape flora, and the importance of the correct sampling strategies. [source] Effects of plant diversity, plant productivity and habitat parameters on arthropod abundance in montane European grasslandsECOGRAPHY, Issue 4 2005Jörg Perner Arthropod abundance has been hypothesized to be correlated with plant diversity but the results of previous studies have been equivocal. In contrast, plant productivity, vegetation structure, abiotic site conditions, and the physical disturbance of habitats, are factors that interact with plant diversity, and that have been shown to influence arthropod abundance. We studied the combined effect of plant species diversity, productivity and site characteristics on arthropod abundance in 71 managed grasslands in central Germany using multivariate statistics. For each site we determined plant species cover, plant community biomass (productivity), macro- and micronutrients in the soil, and characterized the location of sites with respect to orographic parameters as well as the current and historic management regimes. Arthropods were sampled using a suction sampler and classified a priori into functional groups (FGs). We found that arthropod abundance was not correlated with plant species richness, effective diversity or Camargo's evenness, even when influences of environmental variables were taken into account. In contrast, plant community composition was highly correlated with arthropod abundances. Plant community productivity influenced arthropod abundance but explained only a small proportion of the variance. The abundances of the different arthropod FGs were influenced differentially by agricultural management, soil characteristics, vegetation structure and by interactions between different FGs of arthropods. Herbivores, carnivores and detritivores reacted differently to variation in environmental variables in a manner consistent with their feeding mode. Our results show that in natural grassland systems arthropod abundance is not a simple function of plant species richness, and they emphasize the important role of plant community composition for the abundance patterns of the arthropod assemblages. [source] Relationships between spatial environmental heterogeneity and plant species diversity on a limestone pavementECOGRAPHY, Issue 6 2003Jeremy T. Lundholm No empirical studies have examined the relationship between diversity and spatial heterogeneity across unimodal species richness gradients. We determined the relationships between diversity and environmental factors for 144 0.18 m2 plots in a limestone pavement alvar in southern Ontario, Canada, including within-plot spatial heterogeneity in soil depth, microtopography and microsite composition. Species richness was unimodally related to mean soil depth and relative elevation. Microsite heterogeneity and soil depth heterogeneity were positively correlated with species richness, and the richness peaks of the unimodal gradients correspond to the maximally spatially heterogeneous plots. The best predictive models of species richness and evenness, however, showed that other factors, such as ramet density and flooding, are the major determinants of diversity in this system. The findings that soil depth heterogeneity had effects on diversity when the effects of mean soil depth were factored out, and that unimodal richness peaks were associated with high spatial heterogeneity in environmental factors represent significant contributions to our understanding of how spatial heterogeneity might contribute to diversity maintenance in plant communities. [source] Responses of global plant diversity capacity to changes in carbon dioxide concentration and climateECOLOGY LETTERS, Issue 11 2008F. I. Woodward Abstract We model plant species diversity globally by country to show that future plant diversity capacity has a strong dependence on changing climate and carbon dioxide concentration. CO2 increase, through its impact on net primary production and warming is predicted to increase regional diversity capacity, while warming with constant CO2 leads to decreases in diversity capacity. Increased CO2 concentrations are unlikely to counter projected extinctions of endemic species, shown in earlier studies to be more strongly dependent on changing land use patterns than climate per se. Model predictions were tested against (1) contemporary observations of tree species diversity in different biomes, (2) an independent global map of contemporary species diversity and (3) time sequences of plant naturalisation for different locations. Good agreements between model, observations and naturalisation patterns support the suggestion that future diversity capacity increases are likely to be filled from a ,cosmopolitan weed pool' for which migration appears to be an insignificant barrier. [source] Do biotic interactions shape both sides of the humped-back model of species richness in plant communities?ECOLOGY LETTERS, Issue 7 2006Richard Michalet Abstract A humped-back relationship between species richness and community biomass has frequently been observed in plant communities, at both local and regional scales, although often improperly called a productivity,diversity relationship. Explanations for this relationship have emphasized the role of competitive exclusion, probably because at the time when the relationship was first examined, competition was considered to be the significant biotic filter structuring plant communities. However, over the last 15 years there has been a renewed interest in facilitation and this research has shown a clear link between the role of facilitation in structuring communities and both community biomass and the severity of the environment. Although facilitation may enlarge the realized niche of species and increase community richness in stressful environments, there has only been one previous attempt to revisit the humped-back model of species richness and to include facilitative processes. However, to date, no model has explored whether biotic interactions can potentially shape both sides of the humped-back model for species richness commonly detected in plant communities. Here, we propose a revision of Grime's original model that incorporates a new understanding of the role of facilitative interactions in plant communities. In this revised model, facilitation promotes diversity at medium to high environmental severity levels, by expanding the realized niche of stress-intolerant competitive species into harsh physical conditions. However, when environmental conditions become extremely severe the positive effects of the benefactors wane (as supported by recent research on facilitative interactions in extremely severe environments) and diversity is reduced. Conversely, with decreasing stress along the biomass gradient, facilitation decreases because stress-intolerant species become able to exist away from the canopy of the stress-tolerant species (as proposed by facilitation theory). At the same time competition increases for stress-tolerant species, reducing diversity in the most benign conditions (as proposed by models of competition theory). In this way our inclusion of facilitation into the classic model of plant species diversity and community biomass generates a more powerful and richer predictive framework for understanding the role of plant interactions in changing diversity. We then use our revised model to explain both the observed discrepancies between natural patterns of species richness and community biomass and the results of experimental studies of the impact of biodiversity on the productivity of herbaceous communities. It is clear that explicit consideration of concurrent changes in stress-tolerant and competitive species enhances our capacity to explain and interpret patterns in plant community diversity with respect to environmental severity. [source] Top predator control of plant biodiversity and productivity in an old-field ecosystemECOLOGY LETTERS, Issue 2 2003Oswald J. Schmitz Abstract Predators can have strong indirect effects on plants by altering the way herbivores impact plants. Yet, many current evaluations of plant species diversity and ecosystem function ignore the effects of predators and focus directly on the plant trophic level. This report presents results of a 3-year field experiment in a temperate old-field ecosystem that excluded either predators, or predators and herbivores and evaluated the consequence of those manipulations on plant species diversity (richness and evenness) and plant productivity. Sustained predator and predator and herbivore exclusion resulted in lower plant species evenness and higher plant biomass production than control field plots representing the intact natural ecosystem. Predators had this diversity-enhancing effect on plants by causing herbivores to suppress the abundance of a competitively dominant plant species that offered herbivores a refuge from predation risk. [source] Indication of antagonistic interaction between climate change and erosion on plant species richness and soil properties in semiarid Mediterranean ecosystemsGLOBAL CHANGE BIOLOGY, Issue 2 2009PATRICIO GARCÍA-FAYOS Abstract We analyzed the consequences of climate change and the increase in soil erosion, as well as their interaction on plant and soil properties in semiarid Mediterranean shrublands in Eastern Spain. Current models on drivers of biodiversity change predict an additive or synergistic interaction between drivers that will increase the negative effects of each one. We used a climatic gradient that reproduces the predicted climate changes in temperature and precipitation for the next 40 years of the wettest and coldest end of the gradient; we also compared flat areas with 20° steep hillslopes. We found that plant species richness and plant cover are negatively affected by climate change and soil erosion, which in turn negatively affects soil resistance to erosion, nutrient content and water holding capacity. We also found that plant species diversity correlates weakly with plant cover but strongly with soil properties related to fertility, water holding capacity and resistance to erosion. Conversely, these soil properties correlate weaker with plant species cover. The joint effect of climate change and soil erosion on plant species richness and soil characteristics is antagonistic. That is, the absolute magnitude of change is smaller than the sum of both effects. However, there is no interaction between climate change and soil erosion on plant cover and their effects fit the additive model. The differences in the interaction model between plant cover and species richness supports the view that several soil properties are more linked to the effect that particular plant species have on soil processes than to the quantity and quality of the plant cover and biomass they support. Our findings suggest that plant species richness is a better indicator than plant cover of ecosystems services related with soil development and protection to erosion in semiarid Mediterranean climates. [source] Contrasting response of native and alien plant species richness to environmental energy and human impact along alpine elevation gradientsGLOBAL ECOLOGY, Issue 6 2009Lorenzo Marini ABSTRACT Aim, We tested whether the species,energy and species,human relationships vary between native and both naturalized and casual alien species richness when other environmental variables had been taken into account. Location, Trento Province, a region (c. 6200 km2) on the southern border of the European Alps (Italy), subdivided into 156 contiguous (c. 37.5 km2) cells and ranging in elevation from 66 to 3769 m. Methods, Data were separated into three subsets, representing richness of natives, naturalized aliens and casual aliens and separately related to temperature, human population and various environmental correlates of plant species diversity. We applied ordinary least squares and simultaneous autoregressive regressions to identify potential contrasting responses of the three plant status subsets and hierarchical partitioning to evaluate the relative importance of the predictor variables. Results, Variation in alien plant species richness along the region was almost entirely explained by temperature and human population density. The relationships were positive but strongly curvilinear. Native species richness was less strongly related to either factor but was positively related to the presence of calcareous bedrock. Native species richness had a decelerating positive relationship with temperature (R2= 55%), whereas naturalized and casual aliens had a positive accelerating relationship explaining 86% and 62% of the variation in richness, respectively. Native species richness had a positive decelerating relationship with population density (R2= 42%), whilst both alien subsets had a positive accelerating relationship. Main conclusions, Alien species richness was higher in areas with the most rich and diverse assemblages of native species. Areas at high altitudes are not especially prone to alien invasion due to energy constraints, low propagule pressure and disturbance, even considering a potential increased in temperature. Thus, if we consider future environmental change, we should expect a stronger response of aliens than natives in the currently warm, urbanized, low-altitude areas than in cold, high-altitude areas where human population density is low. [source] Spatial relationships between intensive land cover and residual plant species diversity in temperate farmed landscapesJOURNAL OF APPLIED ECOLOGY, Issue 6 2006SIMON M. SMART Summary 1In temperate farmed landscapes conservation policies increasingly emphasize large-scale reductions in land-use intensity. Yet despite a managed reversion to more favourable abiotic conditions, depleted regional species pools may prevent the re-assembly of target communities. 2Using national-scale survey data recorded across Great Britain in 1998, we investigated the extent to which grassland indicator plant species persisted on potential refuge habitats across a spatial gradient of intensive land cover in lowland 1-km squares. These habitats comprised road verges, field boundaries, watercourse banks and small biotope fragments. Intensive land cover comprised built land, arable and improved grassland. 3The rate of reduction in indicator species richness across the intensive land cover gradient was significantly lower in all potential refuge features than in surrounding fields and larger areas of habitat. 4The best refuge locations were watercourse banks and small biotopes. In both cases, indicator species richness was higher than adjacent fields at the lowest intensive land cover and stayed higher as intensive land cover increased. 5However, as intensive land cover increased, plant traits associated with higher nutrient availability were more prominently represented among indicator species. 6Although richer assemblages of indicator species persisted on refuge features, population sizes are likely to be small, because of species,area effects, and also vulnerable to nutrient surpluses and reduced or inappropriate disturbance. 7Synthesis and applications. Across the British lowlands, linear landscape features and small habitat fragments can provide limited safe havens for unimproved grassland plant species. However, the identity of refuge features and their species richness and composition are likely to vary with local conditions. Three activities are therefore paramount in assessing their role in larger scale extensification schemes: (i) development of rapid ways of assessing the plant diversity and distribution of refuge features in local areas; (ii) quantification of the risks posed to the viability of residual source populations through implementation of different options for incorporating them into extensification schemes; (iii) maximization of scheme performance by targeting landscapes with sufficient residual diversity to enable increases in population size of the target species in the medium term. [source] Community organization and species richness of ants (Hymenoptera/Formicidae) in Mongolia along an ecological gradient from steppe to Gobi desertJOURNAL OF BIOGEOGRAPHY, Issue 12 2003Martin Pfeiffer Abstract Aim, Ants (Hymenoptera/Formicidae) have strong influences on ecosystems especially in arid regions. However, little is known about ants of the vast steppe and desert regions of Central Asia. Here we provide the first comprehensive study of ant communities in Mongolia, conducted along a north-to-south gradient in climate. We examined ants' distribution patterns, assessed the impact of climatic parameters on community structure and species diversity and investigated the influence of the corresponding communities of plants. Location, Mongolia (Central Asia). Methods, We observed 31,956 ants at seed baits at 11 study sites along a transect from steppe to Gobi desert for which we attained meteorological data (mean yearly precipitation: 197 to 84 mm). Extra sampling was conducted at sugar and protein baits and by the inspection of different microhabitats. Vegetation patterns of each plot were recorded. Statistical evaluation comprised ordination and correlation. Results, We observed 15 species of ants at seed baits. Three faunal complexes of ants could be distinguished by detrended correspondence analysis (DCA): (1) in steppe baits were dominated by Formica - and Myrmica -species, (2) in semi desert we found mostly species of Tetramorium, Myrmica, Proformica, Plagiolepis, and Leptothorax, and (3) in desert Cataglyphis aenescens and Messor aciculatus dominated, and Lasius was exclusively found there. Another 11 rare ant species were sampled by hand and at sugar baits. Altogether five ant species were new to the Mongolian fauna: Cardiocondyla koshewnikovi, Myrmica koreana, Myrmica pisarskii, Polyergus nigerrimus, and Proformica kaszabi. Assignment of taxa to functional groups showed that in steppe cold climate specialists dominated, in semi desert we found mainly opportunists, and in desert hot climate specialists. Several functional groups know from arid zones in other parts of the world were missing. In desert certain species were highly dominant. First DCA scores of ant- and plant-communities were highly correlated with each other and with climatic parameters. While plant species diversity was positively correlated with increasing northern latitude, ant diversity and ant species richness were not correlated with latitude and responded neither to precipitation, nor to any other climatic parameter. Semi desert was a transition zone between steppe and desert, with high species richness. Ant genus composition of the ecotone overlapped with both other regions. However, beta diversity between pairs of plots within this zone was low, indicating a small-scale mosaic pattern. Main conclusions, The ant communities in the Mongolian steppe and desert zones were strongly influenced by low temperatures and differed in many aspects from the ant fauna in other arid ecosystems, especially in terms of species richness, diversity of feeding guilds, and richness of functional groups. [source] Analysis of plant species diversity with respect to island characteristics on the Channel Islands, CaliforniaJOURNAL OF BIOGEOGRAPHY, Issue 3 2000Aaron Moody Abstract Aim Species richness of native, endemic, and exotic plant groups is examined relative to island area, disturbance history, geological history, and other physical characteristics. Of particular interest are the biogeographic factors that underlie (a) differences in species-area and species-isolation relationships between plant groups; and (b) adherence or departure of individual islands and/or plant groups from expected patterns. Location The eight Channel Islands lie along the continental margin between the U.S./Mexico border and Point Conception, CA. They range in size from 2.6 to 249 km2, and are located from 20 to 100 km off the coast. The islands are known for their high degree of plant endemism, and they have undergone a long history of human occupation by indigenous peoples, followed by over a century of intensive grazing and other biotic disturbances. Methods The study is based on linear regression and residual analysis. Cases where individual islands and/or specific plant groups do not adhere to patterns expected under species-area and species-isolation paradigms, are evaluated with respect to other island characteristics that are not captured by considering only island size and isolation. Results All three plant groups exhibit strong, positive relationships between species richness and island size. For native species, the variance that remains after consideration of island size is largely explained by island isolation. For exotic species, residuals from the species-area relationship are unrelated to isolation. For endemic species, residuals from the species-area relationship are negatively related to isolation. Several islands are outliers for endemic and exotic species, for which richness values are not explained by either island area or isolation. Main,conclusions Species-area and species-isolation relationships for native, endemic, and exotic plant groups differ in accordance with hypothesized differences in the biogeographic factors that govern species diversity for these three groups. Most notably, endemic richness increases with isolation, suggesting the influence of this variable on processes of speciation and relictualism. These general relationships persist despite a long and varied history of human activity on the islands. Analysis of residuals suggests that deviations from expected patterns correspond to island-specific biogeographic factors. It is hypothesized that primary among these factors are land-use history, island environmental characteristics, and community-type richness. [source] Plant functional group composition and large-scale species richness in European agricultural landscapesJOURNAL OF VEGETATION SCIENCE, Issue 1 2008Jaan Liira Abstract Question: Which are the plant functional groups responding most clearly to agricultural disturbances? Which are the relative roles of habitat availability, landscape configuration and agricultural land use intensity in affecting the functional composition and diversity of vascular plants in agricultural landscapes? Location: 25 agricultural landscape areas in seven European countries. Methods: We examined the plant species richness and abundance in 4 km × 4 km landscape study sites. The plant functional group classification was derived from the BIOLFLOR database. Factorial decomposition of functional groups was applied. Results: Natural habitat availability and low land use intensity supported the abundance and richness of perennials, sedges, pteridophytes and high nature quality indicator species. The abundance of clonal species, C and S strategists was also correlated with habitat area. An increasing density of field edges explained a decrease in richness of high nature quality species and an increase in richness of annual graminoids. Intensive agriculture enhanced the richness of annuals and low nature quality species. Conclusions: Habitat patch availability and habitat quality are the main drivers of functional group composition and plant species richness in European agricultural landscapes. Linear elements do not compensate for the loss of habitats, as they mostly support disturbance tolerant generalist species. In order to conserve vascular plant species diversity in agricultural landscapes, the protection and enlargement of existing patches of (semi-) natural habitats appears to be more effective than relying on the rescue effect of linear elements. This should be done in combination with appropriate agricultural management techniques to limit the effect of agrochemicals to the fields. [source] Influence of nests of leaf-cutting ants on plant species diversity in road verges of northern PatagoniaJOURNAL OF VEGETATION SCIENCE, Issue 3 2000A.G. Farji-Brener Correa (1969,1998) Abstract. It has been suggested that ant nests are the most frequent small-scale disturbance that affect vegetation patterns. However, their effects on plant diversity are little studied. We document effects of nests of the leaf-cutting ant Acromyrmex lobicornis on physical-chemical soil properties and their influence on plant diversity near road verges in a desert steppe in NW Patagonia, Argentina. We analysed nest soils and controls for nitrogen, phosphorus, organic matter, moisture retention capacity and texture. We also analysed the vegetation on 42 nests (30 active and 12 abandoned or without life) and 42 areas without nests. Soil around nests had a greater nutrient content and capacity to retain moisture than control soils, which is mainly due to the presence of organic waste that the ants deposit on the soil surface. We found no association between the occurrence of nests and specific groups of plants, but plant diversity was higher at nest-sites than at nearby non-nest sites. This increased diversity , which is also found on abandoned nests , is mainly due to the occurrence of a larger number of native and exotic plant species on nest-sites that are uncommon elsewhere in the study area. The most abundant plant species showed similar cover values at nest and non-nest sites. This suggests that changes in diversity are associated to edaphic changes caused by nests rather than by changes in competitive balance caused by dominant species exclusion. We propose that the nests of Acromyrmex lobicornis, through increasing the availability of resources, generate favourable microsites that can function both as ,refuges' for less frequent native species, and as,stepping stones' for less frequent exotic plant species. [source] Control of plant species diversity and community invasibility by species immigration: seed richness versus seed densityOIKOS, Issue 1 2003Rebecca L. Brown Immigration rates of species into communities are widely understood to influence community diversity, which in turn is widely expected to influence the susceptibility of ecosystems to species invasion. For a given community, however, immigration processes may impact diversity by means of two separable components: the number of species represented in seed inputs and the density of seed per species. The independent effects of these components on plant species diversity and consequent rates of invasion are poorly understood. We constructed experimental plant communities through repeated seed additions to independently measure the effects of seed richness and seed density on the trajectory of species diversity during the development of annual plant communities. Because we sowed species not found in the immediate study area, we were able to assess the invasibility of the resulting communities by recording the rate of establishment of species from adjacent vegetation. Early in community development when species only weakly interacted, seed richness had a strong effect on community diversity whereas seed density had little effect. After the plants became established, the effect of seed richness on measured diversity strongly depended on seed density, and disappeared at the highest level of seed density. The ability of surrounding vegetation to invade the experimental communities was decreased by seed density but not by seed richness, primarily because the individual effects of a few sown species could explain the observed invasion rates. These results suggest that seed density is just as important as seed richness in the control of species diversity, and perhaps a more important determinant of community invasibility than seed richness in dynamic plant assemblages. [source] Estuarine Restoration of Submersed Aquatic Vegetation: The Nursery Bed EffectRESTORATION ECOLOGY, Issue 4 2010Angela Hengst The historic decline of submersed aquatic vegetation (SAV) in mesohaline regions of Chesapeake Bay, United States involved a diversity of plant species. The recent modest recovery is mostly, however, associated with a single, prolific but ephemeral species, Ruppia maritima. Two previously abundant and more stable species, Potamogeton perfoliatus and Stuckenia pectinata, have shown virtually no evidence of recovery. Based on previous studies that demonstrated the ability of R. maritima stands to enhance water clarity and nutrient conditions for SAV growth, we hypothesized that these beds would serve as effective "nursery" areas to incite transplant success for other SAV. We conducted experiments in a two-phase study at small and large spatial scales designed to explore this "nursery effect" as a restoration approach to increase plant species diversity. The first phase was conducted at small spatial scales to test effects of patch density by planting P. perfoliatus and S. pectinata into bare, sparse, and densely vegetated areas within three similar R. maritima beds in a tributary of Chesapeake Bay. Mean seasonal percent survivorship and shoot density were significantly higher in bare patches compared to vegetated patches. In the second phase of the study, P. perfoliatus was transplanted into separate R. maritima beds of different densities to test the effect of bed scale plant density on P. perfoliatus survival and growth. Transplant success of P. perfoliatus was positively correlated with the density of R. maritima among all sites. [source] Impacts of Restored Patch Density and Distance from Natural Forests on Colonization SuccessRESTORATION ECOLOGY, Issue 4 2003Hans Jacquemyn Abstract The reduction and fragmentation of forest habitats is expected to have profound effects on plant species diversity as a consequence of the decreased area and increased isolation of the remnant patches. To stop the ongoing process of forest fragmentation, much attention has been given recently to the restoration of forest habitat. The present study investigates restoration possibilities of recently established patches with respect to their geographical isolation. Because seed dispersal events over 100 m are considered to be of long distance, a threshold value of 100 m between recent and old woodland was chosen to define isolation. Total species richness, individual patch species richness, frequency distributions in species occurrences, and patch occupancy patterns of individual species were significantly different among isolated and nonisolated stands. In the short term no high species richness is to be expected in isolated stands. Establishing new forests adjacent to existing woodland ensures higher survival probabilities of existing populations. In the long term, however, the importance of long-distance seed dispersal should not be underestimated because most species showed occasional long-distance seed dispersal. A clear distinction should be made between populations colonizing adjacent patches and patches isolated from old woodland. The colonization of isolated stands may have important effects on the dynamics and diversity of forest networks, and more attention should be directed toward the genetic traits and viability of founding populations in isolated stands. [source] Multi-scale responses of plant species diversity in semi-natural buffer strips to agricultural landscapesAPPLIED VEGETATION SCIENCE, Issue 2 2008Maohua Ma Question: How does agricultural land usage affect plant species diversity in semi-natural buffer strips at multiple scales? Location: Lepsämä River watershed, Nurmijärvi, Southern Finland. Methods: Species diversity indicators included both richness and evenness. Plant communities in buffer strips were surveyed in 29 sampling sites. Using ArcGIS Desktop 9.0 (ArcInfo) and Fragstats 3.3 for GIS analysis, the landscape composition around each sampling site was characterized by seven parameters in square sectors at five scales: 4, 36, 100, 196, and 324ha. For each scale, Principle Component Analysis was used to examine the importance of each structural metric to diversity indicators using multiple regression and other simple analyses. Results: For all but the smallest scales (4 ha), two structural metrics including the diversity of land cover types and percentage of arable land were positively and negatively correlated with species richness, respectively. Both metrics had the highest correlation coefficients for species richness at the second largest scale (196 ha). The density of arable field edges between the fields was the only metric that correlated with species evenness for all scales, which had highest predictive power at the second smallest scale (36 ha). Conclusions: Species richness and evenness of buffer strips had scale-dependent relationships to land use in agricultural ecosystems. The results of this study indicated that species richness depends on the pattern of arable land use at large scales, which may relate to the regional species pool. Meanwhile, species evenness depended on the level of field edge density at small scales, which relates to how the nearby farmland was divided by the edges (e.g. many small-scale fields with high edge density or a few big-scale fields with low edge density). This implies that it is important to manage the biodiversity of buffer strips within a landscape context at multiple scales. [source] The contribution of rewetting to vegetation restoration of degraded peat meadowsAPPLIED VEGETATION SCIENCE, Issue 3 2007J. van Dijk van der Meijden (1990) Abstract Question: What is the contribution of a rise in groundwater level to vegetation restoration of degraded peat meadows compared to abandonment only? Location: Abandoned peat meadows in the central part of The Netherlands. Methods: Comparison of species composition and species abundance of vegetation and seed banks of reference and rewetted peat meadows, using plant trait and seed bank analysis. Results: Vegetation of rewetted meadows shared on average only 27% of their species with the reference meadow, while this was 50% on average for species in the seed bank. Rewetted meadows had a lower total number of species and a lower number of wet grassland and fen species present in the vegetation, but had higher species richness per m2, although evenness was not affected. Rewetting increased the dominance of species of fertile and near neutral habitats, but did not result in an increase of species of wet or waterlogged habitats. Re-wetted meadows were dominated by species relying mainly on vegetative reproduction and species with a low average seed longevity compared to the reference meadow. Conclusion: Rewetting was not effective as a restoration measure to increase plant species diversity or the number of wet grassland and fen species in the vegetation. If no additional restoration management is applied, the seed bank will be depleted of seeds of species of wet grassland or fen habitats, further reducing the chances of successful vegetation restoration. [source] Resilience of a high-conservation-value, semi-arid grassland on fertile clay soils to burning, mowing and ploughingAUSTRAL ECOLOGY, Issue 4 2010TOM LEWIS Abstract In grassland reserves, managed disturbance is often necessary to maintain plant species diversity. We carried out experiments to determine the impact of fire, kangaroo grazing, mowing and disc ploughing on grassland species richness and composition in a nature reserve in semi-arid eastern Australia. Vegetation response was influenced by winter,spring drought after establishment of the experiments, but moderate rainfall followed in late summer,autumn. Species composition varied greatly between sampling times, and the variability due to rainfall differences between seasons and years was greater than the effects of fire, kangaroo grazing, mowing or disc ploughing. In the fire experiment, species richness and composition recovered more rapidly after spring than autumn burning. Species richness and composition were similar to control sites within 12 months of burning and mowing, suggesting that removal of the dominant grass canopy is unnecessary to enhance plant diversity. Two fires (separated by 3 years) and post-fire kangaroo grazing had only minor influence on species richness and composition. Even disc ploughing caused only a small reduction in native richness. The minor impact of ploughing was explained by the small areas that were ploughed, the once-off nature of the treatment, and the high degree of natural movement and cracking in these shrink-swell soils. Recovery of the composition and richness of these grasslands was rapid because of the high proportion of perennial species that resprout vegetatively after fire and mowing. There appears to be little conservation benefit from fire, mowing or ploughing ungrazed areas, as we could identify no native plant species dependent on frequent disturbance for persistence in this grassland community. However, the ability of the Astrebla- and Dichanthium -dominated grasslands to recover quickly after disturbance, given favourable seasonal conditions, suggests that they are well adapted to natural disturbances (e.g. droughts, fire, flooding and native grazing). [source] Stream salinization is associated with reduced taxonomic, but not functional diversity in a riparian plant communityAUSTRAL ECOLOGY, Issue 3 2006ROBERT G. DOUPÉ Abstract Dryland salinity presents an overwhelming threat to terrestrial and aquatic habitats in Australia, and yet there remains very little empirical evidence of the impacts of secondary salinization on the biodiversity of riparian communities. Here we describe the response of a riparian plant community to stream and soil salinization, 25 years after the experimental clearing of a catchment in south-western Australia. Riparian plant species diversity was inversely related to soil salinity, and plant species composition was significantly altered by increased soil salinity. Despite the evidence for an impact of salinization on the taxonomic diversity and composition of the riparian plant community, there was little evidence for any effect of salinization on functional group diversity, or on ecological functioning, as measured by the percentage of above-ground plant cover. [source] Phylogenetic Composition of Angiosperm Diversity in the Cloud Forests of MexicoBIOTROPICA, Issue 4 2010Isolda Luna-Vega ABSTRACT Several members of the most ancient living lineages of flowering plants (angiosperms) inhabit humid, woody, mostly tropical habitats. Here we assess whether one of these forest types, the cloud forests of Mexico (CFM), contain a relatively higher proportion of phylogenetically early-diverging angiosperm lineages. The CFM houses an extraordinary plant species diversity, including members of earliest-diverging angiosperm lineages. The phylogenetic composition of CFM angiosperm diversity was evaluated through the relative representation of orders and families with respect to the global flora, and the predominance of phylogenetically early- or late-diverging lineages. Goodness-of-fit tests indicated significant differences in the proportional local and global representation of angiosperm clades. The net difference between the percentage represented by each order and family in the CFM and the global flora allowed identification of clades that are overrepresented and underrepresented in the CFM. Early-diverging angiosperm orders and families were found to be neither over- nor underrepresented in the CFM. A slight predominance of late-diverging phylogenetic levels among overrepresented clades, however, was encountered in the CFM. The resulting pattern suggests that cloud forests provide habitats where the most ancient angiosperm lineages have survived in the face of accumulating species diversity belonging to phylogenetically late-diverging lineages. Abstract in Spanish is available at http://www.blackwell-synergy.com/loi/btp [source] | |||||||||||||||||||||||||