123 research outputs found
Nitrogen and phosphorus co-limitation and grazing moderate nitrogen impacts on plant growth and nutrient cycling in sand dune grassland
Atmospheric nitrogen (N) deposition alters plant biodiversity and ecosystem function in grasslands worldwide. This study examines the impact of 6 years of nutrient addition and grazing management on a sand dune grassland. Results indicate that co-limitation of N and phosphorus (P) moderates the impact of realistic rates of N addition (7.5, 15 kg N ha−1 year−1). Combined NP addition (15 kg N + 10 kg P ha−1 year−1) was the only nutrient treatment to differ significantly from the control, with greater above-ground biomass (mainly moss), and enhanced N and P mineralisation rates. Grazing management altered plant functional group composition, reduced above-ground biomass and meso-faunal feeding rates, and decoupled N and P mineralisation. There were no synergistic effects of grazing and N treatment. Although NP co-limitation apparently prevents adverse impacts of N deposition above the critical load, excess N is likely to be stored in moss biomass and soil, with unknown future consequences
Methane, carbon dioxide and nitrous oxide fluxes from a temperate salt marsh: grazing management does not alter global warming potential
Soil greenhouse gas emissions from cattle grazed and un-grazed temperate upper salt marsh were measured using dark static chambers, monthly for one year. Below-ground gas sampling tubes were also used to measure soil methane (CH4) concentrations. CH4 efflux from grazed and un-grazed salt marsh did not differ significantly although grazing did lead to ‘hotspots’ of underground CH4 (up to 6% of total air volume) and CH4 efflux (peak of 9 mg m−2 h−1) significantly linked to high soil moisture content, low soil temperatures and the presence of Juncus gerardii. Carbon dioxide (CO2) efflux was greater from the un-grazed marsh (mean of 420 mg m−2 h−1) than the grazed marsh (mean of 333 mg m−2 h−1) throughout most of the year and was positively correlated with the deeper water table and greater soil temperatures. Grazing was not a significant predictor of nitrous oxide (N2O) soil emissions. Global Warming Potential (GWP; over 100 years), calculated from mean yearly chamber fluxes for CH4 and CO2, did not differ significantly with grazing treatment. Seasonal variation in the key drivers of soil greenhouse gas efflux; soil temperature, moisture and water table, plus the presence or absence of aerenchymatous plants such as J. gerardii were more important to the magnitude of greenhouse gas emissions than grazing management per se
Biodiversity, ecosystem function and ecosystem service provision in saltmarsh and sand dune grasslands
Coastal grasslands, such as salt marshes and sand dunes, provide many important ecosystem services including ‘supporting services’ (soil formation, primary productivity and nutrient cycling), ‘provisioning services’ (fresh water supply, food and fibre products, bio-chemical or genetic resources), ‘regulating services’ (equable climate, pollution control, flood prevention, invertebrate pollination and pest regulation) and ‘cultural services’ (recreation, education and aesthetic appreciation). Historically, salt marsh and sand dune grasslands were commonly used as agricultural livestock grazing land. Currently, some of these coastal grasslands are ‘conservation grazed’ (i.e. extensively grazed to maximise plant diversity and to provide a suitable habitat for over-wintering bird species), others have been ‘abandoned’ (i.e. large herbivores removed) due to the removal of agricultural subsidies or remain historically ‘un-grazed’. Grazing management of coastal grasslands influences biological and physical habitat characteristics, ecosystem function, biodiversity and ecosystem service delivery. Understanding the impact of grazing is therefore vital to enable future robust management recommendations. Biodiversity is often used as an indicator of ecosystem health and ecosystem service provision with conservation priorities allocated accordingly. It is therefore essential to critically assess just how important biodiversity is to the provision of ecosystem services within a wide range of habitats. The review chapter draws together evidence for this argument from salt marsh and sand dune habitats with the conclusion that functional diversity and composition are more important than biodiversity per se (Chapter 2). The experimental chapters of this thesis deal with the impact of grazing upon temperate salt marsh and sand dune grassland biodiversity and ecosystem service provision. ‘Grazed’ (cattle grazed < 8 cm) and historically ‘un-grazed’ upper salt marsh plots were compared. ‘Fully grazed’ (ponies 0.2 ha-1, cattle 0.05 ha-1 and rabbits 45 ha-1), ‘rabbit grazed’ and ‘un-grazed’ (for 8 years) fixed sand dune grassland plots were also evaluated. Firstly, how grazing management affected ecosystem service provision of sand dune grassland was examined, by measuring a wide range of biophysical variables as proxies for ecosystem services (Chapter 3). ‘Supporting’ and ‘regulating’ services were provided predominantly by the un-grazed, ‘provisioning’ and ‘cultural’ services by the extensively grazed grassland. Secondly, the impact of short sward cattle grazing on the abundance, composition and diversity of the ground dwelling invertebrate community of an upper salt marsh was assessed using pitfall traps (Chapter 4). The findings showed that both cattle grazed and un-grazed saltmarsh habitat should be maintained to maximise invertebrate abundance and diversity and provide suitable habitat for coastal specialists. Thirdly, greenhouse gas emissions from grazed and un-grazed salt marsh were measured monthly for one year. Additionally, below-ground gas sampling tubes were used to measure soil methane concentrations (Chapter 5). Carbon dioxide efflux was greater from the un-grazed marsh soil but ‘hotspots’ of methane efflux were only found on the grazed marsh. Finally, the influence of grazing on the soil microbial community of both salt marsh and sand dune grasslands was measured by microbial biomass (fatty acid phospholipids: PLFAs), bacterial growth rate (Leucine incorporation) and respiration rates (Chapter 6). Microbial biomass, PLFA markers and bacterial growth rate were all influenced by grazing management. In summary, this work concludes that grazing management clearly affects biological and physical habitat characteristics, biodiversity, ecosystem function and ecosystem service delivery (Chapter 7). Management of coastal grasslands evidently involves trade-offs between biodiversity conservation and multiple ecosystem service provision
Are Drivers of Root-Associated Fungal Community Structure Context Specific?
The composition and structure of plant-root-associated fungal communities are determined by local abiotic and biotic conditions. However, the relative influence and identity of relationships to abiotic and biotic factors may differ across environmental and ecological contexts, and fungal functional groups. Thus, understanding which aspects of root-associated fungal community ecology generalise across contexts is the first step towards a more predictive framework. We investigated how the relative importance of biotic and abiotic factors scale across environmental and ecological contexts using high-throughput sequencing (ca. 55 M Illumina metabarcoding sequences) of >260 plant-root-associated fungal communities from six UK salt marshes across two geographic regions (South-East and North-West England) in winter and summer. Levels of root-associated fungal diversity were comparable with forests and temperate grasslands, quadrupling previous estimates of salt-marsh fungal diversity. Whilst abiotic variables were generally most important, a range of site- and spatial scale-specific abiotic and biotic drivers of diversity and community composition were observed. Consequently, predictive models of diversity trained on one site, extrapolated poorly to others. Fungal taxa from the same functional groups responded similarly to the specific drivers of diversity and composition. Thus site, spatial scale and functional group are key factors that, if accounted for, may lead to a more predictive understanding of fungal community ecology
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