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Highest Species Richness (highest + species_richness)
Selected AbstractsNeophyte species richness at the landscape scale under urban sprawl and climate warmingDIVERSITY AND DISTRIBUTIONS, Issue 6 2009Michael P. Nobis Abstract Aim, Land use and climate are two major components of global environmental change but our understanding of their simultaneous and interactive effects upon biodiversity is still limited. Here, we investigated the relationship between the species richness of neophytes, i.e. non-native vascular plants introduced after 1500 AD, and environmental covariates to draw implications for future dynamics under land-use and climate change. Location, Switzerland, Central Europe. Methods, The distribution of vascular plants was derived from a systematic national grid of 1 km2 quadrates (n = 456; Swiss Biodiversity Monitoring programme) including 1761 species, 122 of which were neophytes. Generalized linear models (GLMs) were used to correlate neophyte species richness with environmental covariates. The impact of land-use and climate change was thereafter evaluated by projections for the years 2020 and 2050 using scenarios of moderate and strong changes for climate warming (IPCC) and urban sprawl (NRP 54). Results, Mean annual temperature and the amount of urban areas explained neophyte species richness best, with a high predictive power of the corresponding model (cross-validated D2 = 0.816). Climate warming had a stronger impact on the potential increase in the mean neophyte species richness (up to 191% increase by 2050) than ongoing urban sprawl (up to 10% increase) independently from variable interactions and model extrapolations to non-analogue environments. Main conclusions, In contrast to other vascular plants, the prediction of neophyte species richness at the landscape scale in Switzerland requires few variables only, and regions of highest species richness of the two groups do not coincide. The neophyte species richness is basically driven by climatic (temperature) conditions, and urban areas additionally modulate small-scale differences upon this coarse-scale pattern. According to the projections climate warming will contribute to the future increase in neophyte species richness much more than ongoing urbanization, but the gain in new neophyte species will be highest in urban regions. [source] Does conservation planning matter in a dynamic and uncertain world?ECOLOGY LETTERS, Issue 8 2004Eli Meir Abstract Loss of biodiversity is one of the world's overriding environmental challenges. Reducing those losses by creating reserve networks is a cornerstone of global conservation and resource management. Historically, assembly of reserve networks has been ad hoc, but recently the focus has shifted to identifying optimal reserve networks. We show that while comprehensive reserve network design is best when the entire network can be implemented immediately, when conservation investments must be staged over years, such solutions actually may be sub-optimal in the context of biodiversity loss and uncertainty. Simple decision rules, such as protecting the available site with the highest irreplaceability or with the highest species richness, may be more effective when implementation occurs over many years. [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] Atlantic reef fish biogeography and evolutionJOURNAL OF BIOGEOGRAPHY, Issue 1 2008S. R. Floeter Abstract Aim, To understand why and when areas of endemism (provinces) of the tropical Atlantic Ocean were formed, how they relate to each other, and what processes have contributed to faunal enrichment. Location, Atlantic Ocean. Methods, The distributions of 2605 species of reef fishes were compiled for 25 areas of the Atlantic and southern Africa. Maximum-parsimony and distance analyses were employed to investigate biogeographical relationships among those areas. A collection of 26 phylogenies of various Atlantic reef fish taxa was used to assess patterns of origin and diversification relative to evolutionary scenarios based on spatio-temporal sequences of species splitting produced by geological and palaeoceanographic events. We present data on faunal (species and genera) richness, endemism patterns, diversity buildup (i.e. speciation processes), and evaluate the operation of the main biogeographical barriers and/or filters. Results, Phylogenetic (proportion of sister species) and distributional (number of shared species) patterns are generally concordant with recognized biogeographical provinces in the Atlantic. The highly uneven distribution of species in certain genera appears to be related to their origin, with highest species richness in areas with the greatest phylogenetic depth. Diversity buildup in Atlantic reef fishes involved (1) diversification within each province, (2) isolation as a result of biogeographical barriers, and (3) stochastic accretion by means of dispersal between provinces. The timing of divergence events is not concordant among taxonomic groups. The three soft (non-terrestrial) inter-regional barriers (mid-Atlantic, Amazon, and Benguela) clearly act as ,filters' by restricting dispersal but at the same time allowing occasional crossings that apparently lead to the establishment of new populations and species. Fluctuations in the effectiveness of the filters, combined with ecological differences among provinces, apparently provide a mechanism for much of the recent diversification of reef fishes in the Atlantic. Main conclusions, Our data set indicates that both historical events (e.g. Tethys closure) and relatively recent dispersal (with or without further speciation) have had a strong influence on Atlantic tropical marine biodiversity and have contributed to the biogeographical patterns we observe today; however, examples of the latter process outnumber those of the former. [source] Species richness,standing crop relationship in stream bryophyte communities: patterns across multiple scalesJOURNAL OF ECOLOGY, Issue 1 2001Risto Virtanen Summary 1,We tested for a unimodal (,hump-backed') relationship between species richness and standing crop at various spatial scales in stream bryophyte communities. Bryophyte species and their biomasses were determined from 20 to 25 quadrats in eight river and six stream sites in northern Finland. 2,Regression analyses revealed a quadratic relationship between richness and biomass in only two of the river sites and a positive correlation in one other. A quadratic relationship was detected in three stream sites and richness increased linearly with biomass in another. 3,We also tested for the hump-shaped pattern across individual stream boulders, representing an elevational gradient from continuously submerged to permanently dry conditions, with an intermediate zone with fluctuating water level. 4,Species richness-standing crop relationship conformed to the hump-backed model only when samples from all three microhabitats were included in the analysis. A significant positive correlation occurred in the exposed low biomass end of the gradient which is characterized by semi-aquatic species, whereas the relationship tended to be negative in permanently submerged areas with high biomass of large canopy-forming species. Quadrats close to the water level had intermediate standing crop and highest species richness. 5,Species dominant at either end of the gradient appeared unable to monopolize space in the intermediate zone where disturbances (e.g. scouring by ice) detach mosses from the substratum, creating vacant gaps for colonization. The unimodal relationship between richness and biomass is likely to occur only in streams that contain large boulders protruding above the water line, thus providing scope for community diversification along very short vertical distances. [source] MARINE ALGAE ASSOCIATED WITH CARIBBEAN ROCKY SHORES, QUINTANA ROO, MEXICOJOURNAL OF PHYCOLOGY, Issue 2001Article first published online: 24 SEP 200 Albert, E. M. & Lehman, R. L. Center for Coastal Studies, Texas A&M University-Corpus Christi, Corpus Christi, TX 78412 USA Rocky shores located on the east coast of the Yucatan Peninsula are typically high-energy habitats associated with fringing or barrier reef systems. They are phytokarstic (iron-shore) consisting of fossiliferous limestone that is composed of stony coral skeletons. This study compares the macroalgae from three rocky shores located on the east coast of the Yucatan Peninsula, Quintana Roo, Mexico. Fifteen 0.25m2 quadrates were randomly placed in the intertidal and subtidal zones and evaluated for dominant algal cover. In addition, fifteen 0.25 m2 quadrates of standing stock material was randomly collected and used to characterize algal composition, species richness, abundance, and biomass. A voucher collection including herbarium mounts and preserved specimens were prepared for all species encountered. Thirty-five species were identified representing three divisions: Rhodophyta, Chlorophyta, and Phaeophyta. Rhodophyta had the highest species richness with a total of fifteen taxa identified. Phaeophyta had the lowest species richness with seven taxa but dominated algal coverage at two of the three sites. Chlorophyta was represented by thirteen species. Species common to all points were represented by Digenia simplex, Laurencia poiteaui, Laurencia sp., Polysiphonia sp., Microdictyon marinum, Halimeda opuntia, Dictyosphaeria cavernosa, Padina sanctae-crucis, and Turbinaria tricostata. [source] Sampling Techniques Influence Understory Plant Trajectories After Restoration: An Example from Ponderosa Pine RestorationRESTORATION ECOLOGY, Issue 4 2003Julie E. Korb Abstract Although there is no one correct technique for sampling vegetation, the sampling design chosen may greatly influence the conclusions researchers can draw from restoration treatments. Considerations when designing vegetation sampling protocol include determining what sampling attributes to measure, the size and shape of the sampling plot, the number of replicates and their location within the study area, and the frequency of sampling. We installed 20 point-intercept transects (50-m long), 8 belt transects (10 × 50 m), 10 adapted Daubenmire transects (four 0.5 × 2-m plots), and 4 modified-Whittaker plots (20 × 50 m with smaller nested plots) in treatment and control units to measure understory herbaceous response in a forest restoration experiment that tested different treatments. Point-intercept transects on average recorded at least twice as much plant cover as did adapted Daubenmire transects and modified-Whittaker plots taken at the same location for all control and treatment units. Point-intercept transects and adapted Daubenmire plots on average captured fewer rare and exotic species in the control and treatment units in comparison with the belt transects and modified-Whittaker plots. Modified-Whittaker plots captured the highest species richness in all units. Early successional understory response to restoration treatments was likely masked by the response of the herbaceous community to yearly climatic variation (dry vs. wet years). Species richness and abundance were higher in wet years than dry years for all control and treatment units. Our results illustrate that sampling techniques can greatly influence perceptions of understory plant trajectories and therefore the interpretation of whether restoration goals have been achieved. In addition, our results suggest that restoration monitoring needs to be conducted for a sufficient length of time so that restoration treatment responses can be detected. [source] Bird responses to fire severity and time since fire in managed mountain rangelandsANIMAL CONSERVATION, Issue 3 2010P. Pons Abstract Broom matorrals are subjected to extensive burning in the Pyrenees to improve grazing value, despite being a habitat of conservation interest in Europe. Our aim here is to evaluate the impact of such management practices over the long term, and of fire severity over the short term, on avifauna. Bird-habitat stations were distributed in broom shrublands from a few months to 51 years after fire, at 1400,2100 m a.s.l. Overall, shrub cover was the main habitat variable affecting the bird community composition. The abundance trends of bird species for half a century after fire were varied, but population recovery seemed slower (especially in the Dartford warbler Sylvia undata) than it had been reported at a lower altitude. Three species of European conservation concern (Alauda arvensis, Lullula arborea and Lanius collurio) showed abundance peaks at 10,19 years after fire. This time interval showed the highest species richness, abundance and conservation value, whereas shrub cover continued to increase afterwards. The bird assemblage tended to impoverish with increasing fire severity in the first year after a fire. Our results emphasize: (1) the slow recovery of bird community of burnt mountain shrublands; (2) the need for long-term biodiversity assessments to help improve planning of fire intervals at different altitudes; (3) the relevance of reducing fire severity due to its impact on fauna. [source] Tree Diversity, Forest Structure and Productivity along Altitudinal and Topographical Gradients in a Species-Rich Ecuadorian Montane Rain ForestBIOTROPICA, Issue 2 2010Jürgen Homeier ABSTRACT We studied the spatial heterogeneity of tree diversity, and of forest structure and productivity in a highly diverse tropical mountain area in southern Ecuador with the aim of understanding the causes of the large variation in these parameters. Two major environmental gradients, elevation and topography, representing a broad range of climatic and edaphic site conditions, were analyzed. We found the highest species richness of trees in valleys <2100 m. Valleys showed highest values of basal area, leaf area index and tree basal area increment as well. Tree diversity also increased from ridges to valleys, while canopy openness decreased. Significant relationships existed between tree diversity and soil parameters (pH, total contents of Mg, K, Ca, N and P), and between diversity and the spatial variability of pH and Ca and Mg contents suggesting a dependence of tree diversity on both absolute levels and on the small-scale heterogeneity of soil nutrient availability. Tree diversity and basal area increment were positively correlated, partly because both are similarly affected by soil conditions. We conclude that the extraordinarily high tree species richness in the area is primarily caused by three factors: (1) the existence of steep altitudinal and topographic gradients in a rather limited area creating a small-scale mosaic of edaphically different habitats; (2) the intermingling of Amazonian lowland plant species, that reach their upper distribution limits, and of montane forest species; and (3) the geographical position of the study area between the humid eastern Andean slope and the dry interandean forests of South Ecuador. [source] | |||||||||||||||||||