219 research outputs found

    The Performance of Cattle on Lowland Species-Rich Neutral Grassland at Three Contrasting Grazing Pressures

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    Grazing is an essential management practice for maintaining the nature conservation value of lowland semi-natural neutral grassland to control succession and create different faunal habitats via structural heterogeneity within the pasture (Duffey et al., 1974). However, there is a paucity of information on what would constitute a sustainable grazing intensity that will deliver the wildlife objectives and what the consequences of this management would be on growth rate of livestock and overall pasture output. An experiment was designed to quantify the ecological and agronomic consequences of imposing different grazing intensities on species-rich neutral grassland. The results will provide sward-based criteria for the integration of such species-rich grassland into commercial livestock systems

    Enhancing beetle and spider communities in agricultural grasslands: the roles of seed addition and habitat management

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    Over three years, a replicated block design was used to investigate the effects of seed mixtures (grasses only; grasses and legumes; grasses, legumes and non-legume forbs), establishment techniques and long term management on beetle and spider communities of grassland swards. We quantified trophic links between phytophagous beetles and their host plants to assess the effect of these seed mixtures and management practices on food web structure. When managed under low intensity cutting regimes the most diverse seed mixture supported the highest biomass of beetles and spiders (c. 3.6 kg ha−1). Species richness of predatory beetles, phytophagous beetles and spiders were all increased by the sowing of legumes, although the addition of other forbs tended to result in at most modest further increases in invertebrate species richness. Analysis of food web structure suggests that the number of host plants utilised by beetles was greatest within the most diverse seed mixtures, but that this declined rapidly after the establishment year. We demonstrate that by sowing cheap and simple seed mixtures agriculturally improved grasslands can be managed to support increased diversity of spiders and beetles. While seed mixtures do not necessarily need to be of the highest diversity to achieve these benefits, the inclusion of legumes does appear to be crucial. The lower costs of intermediate diversity seed mixtures increase appeal to farmers, increasing the likely uptake of these methodologies in voluntary agri-environment schemes

    The global biogeography of lizard functional groups

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    Aim: Understanding the mechanisms determining species richness is a primary goal of biogeography. Richness patterns of sub-groups within a taxon are usually assumed to be driven by similar processes. However, if richness of distinct ecological strategies respond differently to the same processes, inferences made for an entire taxon may be misleading. We deconstruct the global lizard assemblage into functional groups and examine the congruence among richness patterns between them. We further examine the species richness – functional richness relationship to elucidate the way functional diversity contributes to the overall species richness patterns. Location: Global. Methods: Using comprehensive biological trait databases we classified the global lizard assemblage into ecological strategies based on body size, diet, activity times and microhabitat preferences, using Archetypal Analysis. We then examined spatial gradients in the richness of each strategy at the one-degree grid cell, biomes and realm scales. Results: We found that lizards can best be characterized by seven 'ecological strategies': scansorial, terrestrial, nocturnal, herbivorous, fossorial, large and semiaquatic. There are large differences among the global richness patterns of these strategies. While the major richness hotspot for lizards in general is in Australia, several strategies exhibit highest richness in the Amazon Basin. Importantly, the global maximum in lizard species richness is achieved at intermediate values of functional diversity and increasing functional diversity further result in a shallow decline of species richness. Main conclusions: The deconstruction of the global lizard assemblage along multiple ecological axes offers a new way to conceive lizard diversity patterns. It suggests that local lizard richness mostly increases when species belonging to particular ecological strategies become hyper-diverse there, and not because more ecological types are present in the most species rich localities. Thus maximum richness and maximum ecological diversity do not overlap. These results shed light on the global richness pattern of lizards, and highlight previously unidentified spatial patterns in understudied functional groups
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