Home About us Contact
|
Home About us Contact | ||
|
|
||
Plant Diversity (plant + diversity)
Kinds of Plant Diversity Selected AbstractsGrasshopper Herbivory Affects Native Plant Diversity and Abundance in a Grassland Dominated by the Exotic Grass Agropyron cristatumRESTORATION ECOLOGY, Issue 1 2009David H. Branson Abstract The indirect effects of native generalist insect herbivores on interactions between exotic and native grassland plants have received limited attention. Crested wheatgrass (Agropyron cristatum) is the most common exotic rangeland grass in western North America. Crested wheatgrass communities are resistant to colonization by native plant species and have strong competitive effects on native species, imposing problems for the restoration of native grasslands. Grasshoppers are generalist herbivores that are often abundant in Crested wheatgrass,dominated sites in the northern Great Plains. We conducted two experiments in a Crested wheatgrass,dominated grassland in western North Dakota to test the hypothesis that grasshopper herbivory influences local Crested wheatgrass community composition by impeding native seedlings. Grasshopper herbivory negatively affected the species richness, abundance, and Shannon diversity of native plants in 3 of 4 years. Although additional research is needed to determine if grasshoppers actively select native plants, the effects of grasshopper herbivory may be an important consideration in the restoration of Crested wheatgrass areas. Our findings illustrate the importance of understanding the impact of native generalist invertebrate herbivores on the relationships between exotic and native plants. [source] Plant diversity and land use under organic and conventional agriculture: a whole-farm approachJOURNAL OF APPLIED ECOLOGY, Issue 4 2007R. H. GIBSON Summary 1Organic farming is thought to lead to increased biodiversity and greater sustainability than higher-yielding conventional farming systems. It is usually assumed that organic farms have both larger and higher quality areas of semi-natural habitats, although this assumption has not been unequivocally tested. 2Here we test the hypothesis that in comparison to conventional farms, organic farms have larger areas of semi-natural and boundary vegetation, and organic farms support higher levels of plant abundance, richness and diversity within cropped and semi-natural areas. 3Our study compared whole-farms: 10 organic farms were paired with 10 conventional farms in a complex landscape in the south-west of England. On average, organic farms were 7·3 years post conversion. Plant abundance, species richness and diversity were measured in all crop and non-crop landscape elements on each farm. 4Organic farms had greater total areas of semi-natural habitat (woodland, field margins and hedgerows combined). Woodland area on it's own was also significantly greater. Organic farms had more continuous blocks of woodland (with simpler perimeters than similarly sized patches on conventional farms), whereas woodland on conventional farms often consisted of more linear patches. 5Semi-natural habitats on organic farms did not have higher plant abundance, richness or diversity than their conventional counterparts. The only landscape element that showed a significant increase in plant abundance, richness or diversity was arable fields. 6Synthesis and applications. Even within a complex agricultural landscape differences do exist between organic and conventional farms, these differences being larger areas of semi-natural habitats on organic farms. However, with the exception of arable fields, no habitats on organic farms were yet of a better quality than their conventional counterparts in terms of plant abundance and diversity. Conventional farmers may be able to achieve an increase in plant diversity within arable fields by adopting some organic management practices at the field scale (e.g. exclusion of synthetic herbicides), and whole-farm conversion to organic practice might not be required. However, further work is needed to determine any biodiversity benefits of larger areas of semi-natural habitat on conventional farmland. [source] Plant diversity and endemism in sub-Saharan tropical AfricaJOURNAL OF BIOGEOGRAPHY, Issue 2 2001Linder Aim This paper has as its central aim the location of centres of species richness and endemism in the sub-Saharan African flora. Previous postulation of these centres has been based on an intuitive interpretation of distributional data; this paper provides a test of these centres. A second aim is to establish whether the two indices, richness and endemism, locate the same centres. Thirdly the relationship between species richness and endemism, and latitude and rainfall are explored. Location The study area includes much of sub-Saharan Africa, but excludes the species-poor southern margin of the Sahara and the Namib,Kalahari regions. Methods Analyses were based on 1818 species, scored on a 2.5 × 2.5 degree grid. Species richness was inferred from a simple grid-diversity count; endemism was determined by three measures: the number of species restricted to two grids, the sum of the inverse of the ranges of the component species of each grid, and the proportion of the species in each grid that have restricted ranges. Results The African flora shows a remarkably profound patterning, both in species richness and endemism. The two measures locate largely the same centres, although the rank order among them differs. These centres are: the Cape Floristic Region, East Coast, Congo-Zambezi watershed, Kivu, Upper and Lower Guinea. Richness is strongly related to maximum rainfall, but there are no obvious correlations between modern climate and endemism. Species richness and endemism north of the equator is much more concentrated into centres than south of the equator. Main conclusions There are strongly developed refugia in sub-Saharan Africa. North of the equator, these refugia are sharply delimited and rather small, separated by large areas of very low endemism. South of the equator endemism tends to be more generally distributed. Variation in species richness in sub-Saharan Africa can be explained largely by modern rainfall, while endemism may be related to palaeoclimatic fluctuations. Both species richness and endemism show a strong skewing towards the south, indicating that the fluctuations in the Sahara might have influenced the modern distribution of plants in Africa. [source] Dispersal limitation may result in the unimodal productivity-diversity relationship: a new explanation for a general patternJOURNAL OF ECOLOGY, Issue 1 2007MEELIS PÄRTEL Summary 1Variation in diversity with habitat productivity has long been a central ecological topic. Plant diversity is mostly highest at intermediate productivity, exhibiting the unimodal (so-called ,hump-back') relationship. This relationship has been explained by both evolutionary and ecological processes, but the potential role of dispersal limitation has not been considered. 2We used European flora data to show that dispersal limitation may contribute to the unimodal productivity-diversity relationship. Species were characterized by their habitat productivity preference and dispersal probability (determined by the number of seeds and the presence of a dispersal syndrome). We calculated average relative dispersal probabilities for species assemblages occurring preferentially in different habitat productivity levels. 3At low productivity levels, species without dispersal syndromes predominate (R2 = 0.89), but at high productivity levels, species with a low number of seeds are common (R2 = 0.89). The total relative dispersal probability, combining both the dispersal probabilities attributable to the number of seeds and to the presence of dispersal syndrome, had a unimodal relationship with habitat productivity (R2 = 0.86). Thus, the unimodal productivity-diversity relationship may arise due to the minimal dispersal limitation of local richness in conditions of moderately low productivity. At very low productivity, the lack of dispersal syndromes may limit dispersal. At high productivity, the low number of seeds may limit dispersal. 4Consequently, in conditions where species pool size and biotic interactions do not vary along productivity gradients, the variation in dispersal probabilities with productivity alone can produce unimodal relationships between diversity and productivity. Thus, dispersal limitation may contribute to the observed diversity pattern and ecosystem functioning to a greater extent than usually assumed. [source] Extinction-Rate Estimates for a Modern Neotropical FloraCONSERVATION BIOLOGY, Issue 5 2002Nigel C. A. Pitman We present the first quantitative estimates of extinction rate in a complete Neotropical flora based on historical plant-collection records, quantitative measurements of forest loss and plant diversity, and the conservation status of endemic plant species in Ecuador. Our analyses suggest that 19,46 endemic plant species have gone extinct in Ecuador over the last 250 years, mostly because of habitat loss, and therefore are now globally extinct. An additional 282 species, nearly 7% of Ecuador's endemic flora, qualify as critically endangered. We found evidence of impending large-scale plant extinctions in the country's coastal and Andean forests, but little extinction and low potential for extinction in the Amazonian lowlands. Resumen: Las preocupaciones sobre las elevadas tasas de extinción en los trópicos son una característica común en la literatura sobre conservación, pero las mediciones directas son escasas. Presentamos las primeras estimaciones cuantitativas de la tasa de extinción en una flora neotropical completa basada en los expedientes históricos de colecciones de plantas, las mediciones cuantitativas de la pérdida de bosque y de diversidad y el estado de conservación de especies de plantas endémicas en Ecuador. Nuestro análisis sugiere que 19,46 especies de plantas se han extinguido en el Ecuador a lo largo de los últimos 250 años, debido principalmente a la pérdida de hábitat y por lo tanto son ahora extintas a nivel mundial. Además 282 especies, cerca del 7% de la flora endémica del Ecuador califica como críticamente amenazada. Encontramos indicaciones de inminentes extinciones de gran escala en el país, tanto en los bosques costeros como en los bosques de los Andes, pero poca extinción y bajo potencial de extinción en las tierras bajas del Amazonas. [source] Do cities export biodiversity?DIVERSITY AND DISTRIBUTIONS, Issue 1 2008Traffic as dispersal vector across urban, rural gradients ABSTRACT Urban areas are among the land use types with the highes richness in plant species. A main feature of urban floras is the high proportion of non-native species with often divergent distribution patterns along urban,rural gradients. Urban impacts on plant species richness are usually associated with increasing human activity along rural-to-urban gradients. As an important stimulus of urban plant diversity, human-mediated seed dispersal may drive the process of increasing the similarity between urban and rural floras by moving species across urban,rural gradients. We used long motorway tunnels as sampling sites for propagules that are released by vehicles to test for the impact of traffic on seed dispersal along an urban,rural gradient. Opposite lanes of the tunnels are separated by solid walls, allowing us to differentiate seed deposition associated with traffic into vs. out of the city. Both the magnitude of seed deposition and the species richness in seed samples from two motorway tunnels were higher in lanes leading out of the city, indicating an ,export' of urban biodiversity by traffic. As proportions of seeds of non-native species were also higher in the outbound lanes, traffic may foster invasion processes starting from cities to the surrounding landscapes. Indicator species analysis revealed that only a few species were confined to samples from lanes leading into the city, while mostly species of urban habitats were significantly associated with samples from the outbound lanes. The findings demonstrate that dispersal by traffic reflects different seed sources that are associated with different traffic directions, and traffic may thus exchange propagules along the urban,rural gradient. [source] A simulation approach to determine statistical significance of species turnover peaks in a species-rich tropical cloud forestDIVERSITY AND DISTRIBUTIONS, Issue 6 2007K. Bach ABSTRACT Use of ,-diversity indices in the study of spatial distribution of species diversity is hampered by the difficulty of applying significance tests. To overcome this problem we used a simulation approach in a study of species turnover of ferns, aroids, bromeliads, and melastomes along an elevational gradient from 1700 m to 3400 m in a species-rich tropical cloud forest of Bolivia. Three parameters of species turnover (number of upper/lower elevational species limits per elevational step, Wilson,Shmida similarity index between adjacent steps) were analysed. Significant species turnover limits were detected at 2000 (± 50) m and 3050 m, which roughly coincided with the elevational limits of the main vegetation types recognized in the study area. The taxon specificity of elevational distributions implies that no single plant group can be used as a reliable surrogate for overall plant diversity and that the response to future climate change will be taxon-specific, potentially leading to the formation of plant communities lacking modern analogues. Mean elevational range size of plant species was 490 m (± 369). Elevational range sizes of terrestrial species were shorter than those of epiphytes. We conclude that our simulation approach provides an alternative approach for assessing the statistical significance of levels of species turnover along ecological gradient without the limitations imposed by traditional statistical approaches. [source] Rapid plant diversity assessment using a pixel nested plot design: A case study in Beaver Meadows, Rocky Mountain National Park, Colorado, USADIVERSITY AND DISTRIBUTIONS, Issue 4 2007Mohammed A. Kalkhan ABSTRACT Geospatial statistical modelling and thematic maps have recently emerged as effective tools for the management of natural areas at the landscape scale. Traditional methods for the collection of field data pertaining to questions of landscape were developed without consideration for the parameters of these applications. We introduce an alternative field sampling design based on smaller unbiased random plot and subplot locations called the pixel nested plot (PNP). We demonstrate the applicability of the PNP design of 15 m × 15 m to assess patterns of plant diversity and species richness across the landscape at Rocky Mountain National Park (RMNP), Colorado, USA in a time (cost)-efficient manner for field data collection. Our results produced comparable results to a previous study in the Beaver Meadow study (BMS) area within RMNP, where there was a demonstrated focus of plant diversity. Our study used the smaller PNP sampling design for field data collection which could be linked to geospatial information data and could be used for landscape-scale analyses and assessment applications. In 2003, we established 61 PNP in the eastern region of RMNP. We present a comparison between this approach using a sub-sample of 19 PNP from this data set and 20 of Modified Whittaker nested plots (MWNP) of 20 m × 50 m that were collected in the BMS area. The PNP captured 266 unique plant species while the MWNP captured 275 unique species. Based on a comparison of PNP and MWNP in the Beaver Meadows area, RMNP, the PNP required less time and area sampled to achieve a similar number of species sampled. Using the PNP approach for data collection can facilitate the ecological monitoring of these vulnerable areas at the landscape scale in a time- and therefore cost-effective manner. [source] Potential impacts of climate change on Sub-Saharan African plant priority area selectionDIVERSITY AND DISTRIBUTIONS, Issue 6 2006Colin J. McClean ABSTRACT The Global Strategy for Plant Conservation (GSPC) aims to protect 50% of the most important areas for plant diversity by 2010. This study selects sets of 1-degree grid cells for 37 sub-Saharan African countries on the basis of a large database of plant species distributions. We use two reserve selection algorithms that attempt to satisfy two of the criteria set by the GSPC. The grid cells selected as important plant cells (IPCs) are compared between algorithms and in terms of country and continental rankings between cells. The conservation value of the selected grid cells are then considered in relation to their future species complement given the predicted climate change in three future periods (2025, 2055, and 2085). This analysis uses predicted climate suitability for individual species from a previous modelling exercise. We find that a country-by-country conservation approach is suitable for capturing most, but not all, continentally IPCs. The complementarity-based reserve selection algorithms suggest conservation of a similar set of grid cells, suggesting that areas of high plant diversity and rarity may be well protected by a single pattern of conservation activity. Although climatic conditions are predicted to deteriorate for many species under predicted climate change, the cells selected by the algorithms are less affected by climate change predictions than non-selected cells. For the plant species that maintain areas of climatic suitability in the future, the selected set will include cells with climate that is highly suitable for the species in the future. The selected cells are also predicted to conserve a large proportion of the species richness remaining across the continent under climate change, despite the network of cells being less optimal in terms of future predicted distributions. Limitations to the modelling are discussed in relation to the policy implications for those implementing the GSPC. [source] Negative per capita effects of purple loosestrife and reed canary grass on plant diversity of wetland communitiesDIVERSITY AND DISTRIBUTIONS, Issue 4 2006Shon S. Schooler ABSTRACT Invasive plants can simplify plant community structure, alter ecosystem processes and undermine the ecosystem services that we derive from biotic diversity. Two invasive plants, purple loosestrife (Lythrum salicaria) and reed canary grass (Phalaris arundinacea), are becoming the dominant species in many wetlands across temperate North America. We used a horizontal, observational study to estimate per capita effects (PCEs) of purple loosestrife and reed canary grass on plant diversity in 24 wetland communities in the Pacific Northwest, USA. Four measures of diversity were used: the number of species (S), evenness of relative abundance (J), the Shannon,Wiener index (H,) and Simpson's index (D). We show that (1) the PCEs on biotic diversity were similar for both invasive species among the four measures of diversity we examined; (2) the relationship between plant diversity and invasive plant abundance ranges from linear (constant slope) to negative exponential (variable slope), the latter signifying that the PCEs are density-dependent; (3) the PCEs were density-dependent for measures of diversity sensitive to the number of species (S, H,, D) but not for the measure that relied solely upon relative abundance (J); and (4) invader abundance was not correlated with other potential influences on biodiversity (hydrology, soils, topography). These results indicate that both species are capable of reducing plant community diversity, and management strategies need to consider the simultaneous control of multiple species if the goal is to maintain diverse plant communities. [source] Does plant richness influence animal richness?: the mammals of Catalonia (NE Spain)DIVERSITY AND DISTRIBUTIONS, Issue 4 2004Bradford A. Hawkins ABSTRACT Although it has long been held that plant diversity must influence animal diversity, the nature of this relationship remains poorly understood at large spatial scales. We compare the species richness patterns of vascular plants and mammals in north-eastern Spain using a 100-km2 grain size to examine patterns of covariation. We found that the total mammal richness pattern, as well as those of herbivores and carnivores considered separately, only weakly corresponded to the pattern of plants. Rather, mammal richness was best described by climatic variables incorporating water inputs, and after adding these variables to multiple regression models, plant and mammal richness were virtually independent. We conclude that the observed association, although weak, is explained by shared responses of both groups to climate, and thus, plant richness has no influence on the richness pattern of Catalan mammals. [source] Management strategies for plant invasions: manipulating productivity, disturbance, and competitionDIVERSITY AND DISTRIBUTIONS, Issue 3 2004Michael A. Huston ABSTRACT The traditional approach to understanding invasions has focused on properties of the invasive species and of the communities that are invaded. A well-established concept is that communities with higher species diversity should be more resistant to invaders. However, most recently published field data contradict this theory, finding instead that areas with high native plant diversity also have high exotic plant diversity. An alternative environment-based approach to understanding patterns of invasions assumes that native and exotic species respond similarly to environmental conditions, and thus predicts that they should have similar patterns of abundance and diversity. Establishment and growth of native and exotic species are predicted to vary in response to the interaction of plant growth rates with the frequency and intensity of mortality-causing disturbances. This theory distinguishes between the probability of establishment and the probability of dominance, predicting that establishment should be highest under unproductive and undisturbed conditions and also disturbed productive conditions. However, the probability of dominance by exotic species, and thus of potential negative impacts on diversity, is highest under productive conditions. The theory predicts that a change in disturbance regime can have opposite effects in environments with contrasting levels of productivity. Manipulation of productivity and disturbance provides opportunities for resource managers to influence the interactions among species, offering the potential to reduce or eliminate some types of invasive species. [source] Heterogeneity, speciation/extinction history and climate: explaining regional plant diversity patterns in the Cape Floristic RegionDIVERSITY AND DISTRIBUTIONS, Issue 3 2002R. M. Cowling Abstract. This paper investigates the role of heterogeneity and speciation/extinction history in explaining variation in regional scale (c. 0.1,3000 km2) plant diversity in the Cape Floristic Region of south-western Africa, a species- and endemic-rich biogeographical region. We used species-area analysis and analysis of covariance to investigate geographical (east vs. west) and topographic (lowland vs. montane) patterns of diversity. We used community diversity as a surrogate for biological heterogeneity, and the diversity of naturally rare species in quarter degree squares as an indicator of differences in speciation/extinction histories across the study region. We then used standard statistical methods to analyse geographical and topographic patterns of these two measures. There was a clear geographical diversity pattern (richer in the west), while a topographic pattern (richer in mountains) was evident only in the west. The geographical boundary coincided with a transition from the reliable winter-rainfall zone (west) to the less reliable non-seasonal rainfall zone (east). Community diversity, or biological heterogeneity, showed no significant variation in relation to geography and topography. Diversity patterns of rare species mirrored the diversity pattern for all species. We hypothesize that regional diversity patterns are the product of different speciation and extinction histories, leading to different steady-state diversities. Greater Pleistocene climatic stability in the west would have resulted in higher rates of speciation and lower rates of extinction than in the east, where for the most, Pleistocene climates would not have favoured Cape lineages. A more parsimonious hypothesis is that the more predictable seasonal rainfall of the west would have favoured non-sprouting plants and that this, in turn, resulted in higher speciation and lower extinction rates. Both hypotheses are consistent with the higher incidence of rare species in the west, and higher levels of beta and gamma diversity there, associated with the turnover of species along environmental and geographical gradients, respectively. These rare species do not contribute to community patterns; hence, biological heterogeneity is uniform across the region. The weak topography pattern of diversity in the west arises from higher speciation rates and lower extinction rates in the topographically complex mountains, rather than from the influence of environmental heterogeneity on diversity. [source] Integrating highly diverse invertebrates into broad-scale analyses of cross-taxon congruence across the PalaearcticECOGRAPHY, Issue 6 2009Andreas Schuldt Our knowledge on broad-scale patterns of biodiversity, as a basis for biogeographical models and conservation planning, largely rests upon studies on the spatial distribution of vertebrates and plants, neglecting large parts of the world's biodiversity. To reassess the generality of these patterns and better understand spatial diversity distributions of invertebrates, we analyzed patterns of species richness and endemism of a hyperdiverse insect taxon, carabid beetles (ca 11 000 Palaearctic species known), and its cross-taxon congruence with well-studied vertebrates (amphibians, reptiles) and plants across 107,units of the Palaearctic. Based on species accumulation curves, we accounted for completeness of the carabid data by separately examining the western (well-sampled) and eastern (partly less well-sampled) Palaearctic and China (deficient data). For the western Palaearctic, we highlight overall centers of invertebrate, vertebrate and plant diversity. Species richness and endemism of carabids were highly correlated with patterns of especially plant and amphibian diversity across large parts of the Palaearctic. For the well-sampled western Palaearctic, hotspots of diversity integrating invertebrates were located in Italy, Spain and Greece. Only analysis of Chinese provinces yielded low congruence between carabids and plants/vertebrates. However, Chinese carabid diversity is only insufficiently known and China features the highest numbers of annual new descriptions of carabids in the Palaearctic. Even based on the incomplete data, China harbors at least 25% of all Palaearctic carabid species. Our study shows that richness and endemism patterns of highly diverse insects can exhibit high congruence with general large scale patterns of diversity inferred from plants/vertebrates and that hotspots derived from the latter can also include a high diversity of invertebrates. In this regard, China qualifies as an outstanding multi-taxon hotspot of diversity, requiring intense biodiversity research and conservation effort. Our findings extend the limited knowledge on broad-scale invertebrate distributions and allow for a better understanding of diversity patterns across a larger range of the world's biodiversity than usually considered. [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] Herbivory enhances positive effects of plant genotypic diversityECOLOGY LETTERS, Issue 5 2010John D. Parker Ecology Letters (2010) 13: 553,563 Abstract Both plant diversity and vertebrate herbivores can impact plant fitness and ecosystem functioning, however their interactions have not been explicitly tested. We manipulated plant genotypic diversity of the native plant Oenothera biennis and monitored its survivorship and lifetime fitness with and without one of its major vertebrate consumers, white-tailed deer Odocoileus virginianus. Intense but unmanipulated herbivory by meadow voles Microtus pennsylvanicus killed over 70% of nearly 4000 experimental plants. However, plants grown in genotypically diverse patches suffered fewer vole attacks and had higher survival and reproductive output than plants in monoculture. Moreover, positive effects of genotypic diversity were enhanced by the presence of deer, indicating a non-additive interaction between diversity and trophic-level complexity. Genetic selection analyses showed that the selective value of ecologically important traits depended on plant diversity and exposure to deer, demonstrating that community complexity can promote fitness through multiple ecologically and evolutionarily important feedbacks. [source] Plant,soil feedbacks: a meta-analytical reviewECOLOGY LETTERS, Issue 9 2008Andrew Kulmatiski Abstract Plants can change soil biology, chemistry and structure in ways that alter subsequent plant growth. This process, referred to as plant,soil feedback (PSF), has been suggested to provide mechanisms for plant diversity, succession and invasion. Here we use three meta-analytical models: a mixed model and two Bayes models, one correcting for sampling dependence and one correcting for sampling and hierarchical dependence (delta-splitting model) to test these hypotheses. All three models showed that PSFs have medium to large negative effects on plant growth, and especially grass growth, the life form for which we had the most data. This supports the hypothesis that PSFs, through negative frequency dependence, maintain plant diversity, especially in grasslands. PSFs were also large and negative for annuals and natives, but the delta-splitting model indicated that more studies are needed for these results to be conclusive. Our results support the hypotheses that PSFs encourage successional replacements and plant invasions. Most studies were performed using monocultures of grassland species in greenhouse conditions. Future research should examine PSFs in plant communities, non-grassland systems and field conditions. [source] The unseen majority: soil microbes as drivers of plant diversity and productivity in terrestrial ecosystemsECOLOGY LETTERS, Issue 3 2008Marcel G. A. Van Der Heijden Abstract Microbes are the unseen majority in soil and comprise a large portion of life's genetic diversity. Despite their abundance, the impact of soil microbes on ecosystem processes is still poorly understood. Here we explore the various roles that soil microbes play in terrestrial ecosystems with special emphasis on their contribution to plant productivity and diversity. Soil microbes are important regulators of plant productivity, especially in nutrient poor ecosystems where plant symbionts are responsible for the acquisition of limiting nutrients. Mycorrhizal fungi and nitrogen-fixing bacteria are responsible for c. 5,20% (grassland and savannah) to 80% (temperate and boreal forests) of all nitrogen, and up to 75% of phosphorus, that is acquired by plants annually. Free-living microbes also strongly regulate plant productivity, through the mineralization of, and competition for, nutrients that sustain plant productivity. Soil microbes, including microbial pathogens, are also important regulators of plant community dynamics and plant diversity, determining plant abundance and, in some cases, facilitating invasion by exotic plants. Conservative estimates suggest that c. 20 000 plant species are completely dependent on microbial symbionts for growth and survival pointing to the importance of soil microbes as regulators of plant species richness on Earth. Overall, this review shows that soil microbes must be considered as important drivers of plant diversity and productivity in terrestrial ecosystems. [source] Community maturity, species saturation and the variant diversity,productivity relationships in grasslandsECOLOGY LETTERS, Issue 12 2006Qinfeng Guo Abstract Detailed knowledge of the relationship between plant diversity and productivity is critical for advancing our understanding of ecosystem functioning and for achieving success in habitat restoration efforts. However, effects and interactions of diversity, succession and biotic invasions on productivity remain elusive. We studied newly established communities in relation to preexisting homogeneous vegetation invaded by exotic plants in the northern Great Plains, USA, at four study sites for 3 years. We observed variant diversity,productivity relationships for the seeded communities (generally positive monotonic at three sites and non-monotonic at the other site) but no relationships for the resident community or the seeded and resident communities combined at all sites and all years. Community richness was enhanced by seeding additional species but productivity was not. The optimal diversity (as indicated by maximum productivity) changed among sites and as the community developed. The findings shed new light on ecosystem functioning of biodiversity under different conditions and have important implications for restoration. [source] Magnitude and variability of process rates in fungal diversity-litter decomposition relationshipsECOLOGY LETTERS, Issue 11 2005Christian K. Dang Abstract There is compelling evidence that losses in plant diversity can alter ecosystem functioning, particularly by reducing primary production. However, impacts of biodiversity loss on decomposition, the complementary process in the carbon cycle, are highly uncertain. By manipulating fungal decomposer diversity in stream microcosm experiments we found that rates of litter decomposition and associated fungal spore production are unaffected by changes in decomposer diversity under benign and harsher environmental conditions. This result calls for caution when generalizing outcomes of biodiversity experiments across systems. In contrast to their magnitude, the variability of process rates among communities increased when species numbers were reduced. This was most likely caused by a portfolio effect (i.e. statistical averaging), with the uneven species distribution typical of natural communities tending to weaken that effect. Curbing species extinctions to maintain ecosystem functioning thus can be important even in situations where process rates are unaffected. [source] Biodiversity loss, trophic skew and ecosystem functioningECOLOGY LETTERS, Issue 8 2003J. Emmett Duffy Abstract Experiments testing biodiversity effects on ecosystem functioning have been criticized on the basis that their random-assembly designs do not reflect deterministic species loss in nature. Because previous studies, and their critics, have focused primarily on plants, however, it is underappreciated that the most consistent such determinism involves biased extinction of large consumers, skewing trophic structure and substantially changing conclusions about ecosystem impacts that assume changing plant diversity alone. Both demography and anthropogenic threats render large vertebrate consumers more vulnerable to extinction, on average, than plants. Importantly, species loss appears biased toward strong interactors among animals but weak interactors among plants. Accordingly, available evidence suggests that loss of a few predator species often has impacts comparable in magnitude to those stemming from a large reduction in plant diversity. Thus, the dominant impacts of biodiversity change on ecosystem functioning appear to be trophically mediated, with important implications for conservation. [source] Mechanisms of positive biodiversity,production relationships: insights provided by ,13C analysis in experimental Mediterranean grassland plotsECOLOGY LETTERS, Issue 5 2001Maria C. Caldeira We investigated the role of water use in a Mediterranean grassland, in which diversity was experimentally manipulated, and a positive relationship was observed between plant species richness and productivity. Soil moisture patterns and stable carbon isotope ratios (,13C) in leaves indicated greater water use by plants growing in species-rich mixtures compared to monocultures. These results suggest that complementarity or facilitation may be the mechanism responsible for the positive relationship between plant diversity and ecosystem processes. [source] The influence of arbuscular mycorrhizae on the relationship between plant diversity and productivityECOLOGY LETTERS, Issue 2 2000John N Klironomos Ecological theory predicts a positive and asymptotic relationship between plant diversity and ecosystem productivity based on the ability of more diverse plant communities to use limiting resources more fully. This is supported by recent empirical evidence. Additionally, in natural ecosystems, plant productivity is often a function of the presence and composition of mycorrhizal associations. Yet, the effect of mycorrhizal fungi on the relationship between plant diversity and productivity has not been investigated. We predict that in the presence of AMF, productivity will saturate at lower levels of species richness because AMF increase the ability of plant species to utilize nutrient resources. In this study we manipulated old-field plant species richness in the presence and absence of two species of AMF. We found that in the absence of AMF, the relationship between plant species richness and productivity is positive and linear. However, in the presence of AMF, the relationship is positive but asymptotic, even though the maximum plant biomass was significantly different between the two AMF treatments. This is consistent with the hypothesis that AMF increase the redundancy of plant species in the productivity of plant communities, and indicates that these symbionts must be considered in future investigations of plant biodiversity and ecosystem function. [source] Effects of an exotic invasive macrophyte (tropical signalgrass) on native plant community composition, species richness and functional diversityFRESHWATER BIOLOGY, Issue 6 2010THAÍSA SALA MICHELAN Summary 1.,The issue of freshwater species being threatened by invasion has become central in conservation biology because inland waters exhibit the highest species richness per unit area, but apparently have the highest extinctions rates on the planet. 2.,In this article, we evaluated the effects of an exotic, invasive aquatic grass (Urochloa subquadripara, tropical signalgrass) on the diversity and assemblage composition of native macrophytes in four Neotropical water bodies (two reservoirs and two lakes). Species cover was assessed in quadrats, and plant biomass was measured in further quadrats, located in sites where tropical signalgrass dominated (D quadrats) and sites where it was not dominant or entirely absent (ND quadrats). The effects of tropical signalgrass on macrophyte species richness, Shannon diversity and number of macrophyte life forms (a surrogate of functional richness) were assessed through regressions, and composition was assessed with a DCA. The effects of tropical signalgrass biomass on the likelihood of occurrence of specific macrophyte life forms were assessed through logistic regression. 3.,Tropical signalgrass had a negative effect on macrophyte richness and Shannon and functional diversity, and also influenced assemblage composition. Emergent, rooted with floating stems and rooted submersed species were negatively affected by tropical signalgrass, while the occurrence of free-floating species was positively affected. 4.,Our results suggest that competition with emergent species and reduction of underwater radiation, which reduces the number of submersed species, counteract facilitation of free-floating species, contributing to a decrease in plant diversity. In addition, homogenisation of plant assemblages shows that tropical signalgrass reduces the beta diversity in the macrophyte community. 5.,Although our results were obtained at fine spatial scales, they are cause for concern because macrophytes are an important part of freshwater diversity. [source] Predicting changes in community composition and ecosystem functioning from plant traits: revisiting the Holy GrailFUNCTIONAL ECOLOGY, Issue 5 2002S. Lavorel Summary 1The concept of plant functional type proposes that species can be grouped according to common responses to the environment and/or common effects on ecosystem processes. However, the knowledge of relationships between traits associated with the response of plants to environmental factors such as resources and disturbances (response traits), and traits that determine effects of plants on ecosystem functions (effect traits), such as biogeochemical cycling or propensity to disturbance, remains rudimentary. 2We present a framework using concepts and results from community ecology, ecosystem ecology and evolutionary biology to provide this linkage. Ecosystem functioning is the end result of the operation of multiple environmental filters in a hierarchy of scales which, by selecting individuals with appropriate responses, result in assemblages with varying trait composition. Functional linkages and trade-offs among traits, each of which relates to one or several processes, determine whether or not filtering by different factors gives a match, and whether ecosystem effects can be easily deduced from the knowledge of the filters. 3To illustrate this framework we analyse a set of key environmental factors and ecosystem processes. While traits associated with response to nutrient gradients strongly overlapped with those determining net primary production, little direct overlap was found between response to fire and flammability. 4We hypothesize that these patterns reflect general trends. Responses to resource availability would be determined by traits that are also involved in biogeochemical cycling, because both these responses and effects are driven by the trade-off between acquisition and conservation. On the other hand, regeneration and demographic traits associated with response to disturbance, which are known to have little connection with adult traits involved in plant ecophysiology, would be of little relevance to ecosystem processes. 5This framework is likely to be broadly applicable, although caution must be exercised to use trait linkages and trade-offs appropriate to the scale, environmental conditions and evolutionary context. It may direct the selection of plant functional types for vegetation models at a range of scales, and help with the design of experimental studies of relationships between plant diversity and ecosystem properties. [source] Plant diversity positively affects short-term soil carbon storage in experimental grasslandsGLOBAL CHANGE BIOLOGY, Issue 12 2008SIBYLLE STEINBEISS Abstract Increasing atmospheric CO2 concentration and related climate change have stimulated much interest in the potential of soils to sequester carbon. In ,The Jena Experiment', a managed grassland experiment on a former agricultural field, we investigated the link between plant diversity and soil carbon storage. The biodiversity gradient ranged from one to 60 species belonging to four functional groups. Stratified soil samples were taken to 30 cm depth from 86 plots in 2002, 2004 and 2006, and organic carbon contents were determined. Soil organic carbon stocks in 0,30 cm decreased from 7.3 kg C m,2 in 2002 to 6.9 kg C m,2 in 2004, but had recovered to 7.8 kg C m,2 by 2006. During the first 2 years, carbon storage was limited to the top 5 cm of soil while below 10 cm depth, carbon was lost probably as short-term effect of the land use change. After 4 years, carbon stocks significantly increased within the top 20 cm. More importantly, carbon storage significantly increased with sown species richness (log-transformed) in all depth segments and even carbon losses were significantly smaller with higher species richness. Although increasing species diversity increased root biomass production, statistical analyses revealed that species diversity per se was more important than biomass production for changes in soil carbon. Below 20 cm depth, the presence of one functional group, tall herbs, significantly reduced carbon losses in the beginning of the experiment. Our analysis indicates that plant species richness and certain plant functional traits accelerate the build-up of new carbon pools within 4 years. Additionally, higher plant diversity mitigated soil carbon losses in deeper horizons. This suggests that higher biodiversity might lead to higher soil carbon sequestration in the long-term and therefore the conservation of biodiversity might play a role in greenhouse gas mitigation. [source] What determines the relationship between plant diversity and habitat productivity?GLOBAL ECOLOGY, Issue 6 2008Martin Zobel ABSTRACT The relationship between biodiversity and habitat productivity has been a fundamental topic in ecology. Although the relationship between these parameters may exhibit different shapes, the unimodal shape has been frequently encountered. The decrease in diversity at high productivity has usually been attributed to competitive exclusion. We suggest that evolutionary history and dispersal limitation may be even more important in shaping the diversity,productivity relationship. On a global scale, unimodal diversity,productivity relationships dominate in temperate regions, whereas positive relationships are more common in the tropics. This difference can be accounted for by contrasting evolutionary history. Temperate regions have smaller species pools for productive habitats since these habitats have been scarce historically for speciation, while the opposite is true for the tropics. In addition, dispersal within a region may limit diversity either due to the lack of dispersal syndromes at low productivity or the low number of diaspores at high productivity. Thereafter, biotic interactions (competition and facilitation) can shape the relationship. All these processes can act independently or concurrently. We recommend that the common approach to examining empirical diversity,environmental relationships should start with the role of large-scale processes such as evolutionary history and dispersal limitation, followed by influences associated with ecological interactions. [source] A resource-based conceptual model of plant diversity that reassesses causality in the productivity,diversity relationshipGLOBAL ECOLOGY, Issue 3 2006Chris Lavers ABSTRACT Biogeographical studies frequently reveal positive correlations between species richness and estimates of environmental water and/or energy. A popular interpretation of this relationship relates the supply of water and energy to productivity, and then, in turn, to richness. Productivity,diversity theories are now legion, yet none has proved sufficiently intuitive to gain broad acceptance. Like productivity, heterogeneity is known to influence diversity at fine spatial scales, yet the possibility that richness might relate to water,energy dynamics at coarse spatial scales via a heterogeneity-generating mechanism has received little attention. In this paper we outline such a conceptual model for plants that is internally consistent and testable. We believe it may help to explain the capacity of environments receiving different inputs of water and energy to support variable numbers of species at a range of spatial scales, the pervasive correlation between productivity and richness, some exceptions to the productivity,diversity relationship, the form of productivity,diversity curves and the link between richness and environmental ,harshness'. The model may also provide an answer to one of the most venerable puzzles in the field of diversity studies: why high inputs of water and energy correspond to more species rather than simply more individuals. [source] Effect of livestock breed and grazing intensity on grazing systems: 5.GRASS & FORAGE SCIENCE, Issue 4 2007Management, policy implications Summary This paper explores the management and policy implications of research findings investigating the use of grazing intensity and traditional breeds to achieve biodiversity outcomes on grasslands in four countries of Europe. An economic analysis, based on these research findings, indicated that financial assistance and/or premium prices are required to achieve sustainable grazing systems with a high biodiversity. The research findings suggested that existing agri-environment scheme prescriptions based only on blanket stocking rates are too crude to increase plant diversity, lacking consideration of initial site conditions. Conversely, some invertebrates seem to rapidly benefit from lenient stocking, highlighting the importance of clear goals for agri-environment schemes. Recommendations for an appropriate support package to deliver grazing systems with high biodiversity are presented. [source] Positive and negative effects of livestock grazing on plant diversity of Mongolian nomadic pasturelands along a slope with soil moisture gradientGRASSLAND SCIENCE, Issue 3 2009Noboru Fujita Abstract To examine different effects of herbivorous large mammals' grazing pressure on plant diversity along a slope in a Mongolian nomadic pasture, we compared species richness, Simpson's index of diversity, and the total plant coverage of plants between protected pasture from livestock grazing and grazed pasture on the near ridge, upper slope, lower slope, foot slope and valley bottom. The species richness and Simpson's index of diversity decreased and the total coverage increased downwardly with increase in pasture soil moisture along the slope. The species richness of the protected pasture decreased, changed little, and increased on the near ridge and the upper slope, the lower slope and the foot slope, and the valley bottom, respectively. Simpson's index of diversity of the protected pasture decreased compared with the grazed pasture only on the valley bottom. The total coverage became lower in the grazed pasture. As the reason for our results, we discuss positive and negative effects of livestock grazing on the species diversity of plants. The positive effect is shown on the valley bottom, where soil moisture and plant growth becomes high with the total coverage over 100%, due to relaxing indirectly the competitive exclusion among plants due to the grazing of dominant plants. The negative effect is obtained on the near ridge and the upper slope, where the soil moisture and the plant growth are low, because of elimination of some plants from the pasture by direct grazing damage. [source] | |||||||||||||||||||||||||||||||