389 research outputs found

    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

    Vegetation Re-development After Fen Meadow Restoration by Topsoil Removal and Hay Transfer

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    We investigated the effects of different restoration treatments on the development of fen meadow communities: (1) depth of topsoil removal, with shallow (circa 20 cm) and deep (circa 40 cm) soil removal applied, (2) transfer of seed-containing hay, and (3) access of large animals. We carried out a full factorial experiment with all combinations of these factors and monitored it for 4 years. We studied the effect of seed availability in the soil seed bank on species abundance in the vegetation and compared it to the effect of species introduction by hay. We observed large differences in species composition between different treatments after 4 years. The combination of hay transfer, deep soil removal, and exclusion of large animals resulted in a community with highest similarity to the target vegetation. We found that the transfer of seeds with hay had a larger effect on species abundance than the soil seed bank. Hay transfer appeared to have important consequences on vegetation development because it speeded up the establishment of the target vegetation.

    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

    Bacterial communities associated with honeybee food stores are correlated with land use

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    Microbial communities, associated with almost all metazoans, can be inherited from the environment. Although the honeybee (Apis mellifera L.) gut microbiome is well documented, studies of the gut focus on just a small component of the bee microbiome. Other key areas such as the comb, propolis, honey, and stored pollen (bee bread) are poorly understood. Furthermore, little is known about the relationship between the pollinator microbiome and its environment. Here we present a study of the bee bread microbiome and its relationship with land use. We estimated bacterial community composition using both Illumina MiSeq DNA sequencing and denaturing gradient gel electrophoresis (DGGE). Illumina was used to gain a deeper understanding of precise species diversity across samples. DGGE was used on a larger number of samples where the costs of MiSeq had become prohibitive and therefore allowed us to study a greater number of bee breads across broader geographical axes. The former demonstrates bee bread comprises, on average, 13 distinct bacterial phyla; Bacteroidetes, Firmicutes, Alpha‐proteobacteria, Beta‐proteobacteria, and Gamma‐proteobacteria were the five most abundant. The most common genera were Pseudomonas, Arsenophonus, Lactobacillus, Erwinia, and Acinetobacter. DGGE data show bacterial community composition and diversity varied spatially and temporally both within and between hives. Land use data were obtained from the 2007 Countryside Survey. Certain habitats, such as improved grasslands, are associated with low diversity bee breads, meaning that these environments may be poor sources of bee‐associated bacteria. Decreased bee bread bacterial diversity may result in reduced function within hives. Although the dispersal of microbes is ubiquitous, this study has demonstrated landscape‐level effects on microbial community composition
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