In production horticulture, it is desirable that ground management strategies are selected in such a way as to ensure that there are adequate levels of soil biota present to carry out key ecosystem processes required for long-term crop growth. We established replicated field plots in a New Zealand kiwifruit orchard of each of five ground management treatments, i.e. maintenance of pasture, planting of a dwarf fescue mulch, sawdust application, cultivation and repeated use of herbicides, and then monitored the responses of components of the soil biota to these treatments over a 5-year period. Those treatments involving enhancement of basal resource inputs (pasture, fescue, sawdust) consistently supported higher levels of microbial biomass and activity than did the others. These effects were not consistently propagated through higher trophic levels of the decomposer food web, although populations of microbe-feeding and predacious nematodes did often differ significantly across treatments. This idiosyncratic response of decomposer food web components to treatments is believed to be due to the complex interplay of top-down and bottom-up forces in soil food webs. There were also important treatment effects on nematode community structure; ordination analysis revealed that the sawdust and cultivated plots supported different species assemblages to the pasture and fescue plots. Further, treatments supporting greater basal resource inputs tended to result in a higher diversity of nematodes; on average the Shannon–Weiner diversity index for the 0–5cm depth layer was 2.80 and 2.64 for the fescue and pasture treatments, and only 2.32 and 2.45 for the cultivation and herbicide treatments. Populations of Collembola were also generally enhanced in plots with greater basal resource inputs. We utilised litterbag decomposition rates as a measure of the performance of ecosystem functioning carried out by the soil biota, and generally found that surface placed litter decomposition rates were greatest in those treatments supporting greater levels of basal resource inputs and microbial biomass (i.e. greatest for the mulched and fescue plots, least for the herbicide and cultivated plots), but were generally independent of higher trophic levels. Most of our results could be explained by the fact that treatments differed in the amounts of the basal resources that were likely to be present, rather than other components of agricultural intensification such as direct effects of cultivation-induced disturbance or herbicide toxicity. Finally, our study indicates that in order to gain a more complete picture of how agricultural intensification affects soil biota in the long-term requires experiments which simultaneously consider several trophic levels and several modes of intensification, and which run for several years.
The issue of how plant community composition affects decomposer community composition and function is considered, by reviewing recent literature and through the use of two examples.
Ecologists have studied plant succession for over a hundred years, yet our understanding of the nature of this process is incomplete, particularly in relation to its response to new human perturbations and the need to manipulate it during ecological restoration. We demonstrate how plant succession can be understood better when it is placed in the broadest possible temporal context. We further show how plant succession can be central to the development of a framework that integrates a spectrum of ecological processes, which occur over time scales ranging from seconds to millions of years. This novel framework helps us understand the impacts of human perturbations on successional trajectories, ecosystem recovery, and global environmental change.
Five weed management strategies (sawdust mulching, repeated spring-summer cultivation, hand-hoeing and two herbicide treatments) were applied to each of two cropping systems (maize and asparagus) near Hamilton, New Zealand. Assessments of the response of microbial activity and biomass were made over an entire annual cropping cycle (from August 1990 to October 1991). Soil respiration and substrate-induced respiration (SIR) were strongly stimulated by sawdust mulch over the experimental period, probably as a result of the enhanced soil moisture status, but the other treatments did not exert any strong consistent effects. Use of the selective inhibitor technique demonstrated temporary stimulatory effects of mulching, cultivation and (occasionally) herbicide application on both the bacterial and fungal components of the soil system. The fumigation-incubation technique also suggested that mulching had stimulatory effects on microbial activity and biomass but only when control values were not subtracted. Most of the effects detected occurred in the top 5 cm of the mineral soil. Placement of litter-bags on the surface and at 10cm depth indicated that litter decomposition was often most rapid in the sawdustmulched plots, probably as a result of enhanced abiotic decomposition. Soil respiration and SIR were also greatest for the litter placed on the mulched plots, over most of the annual cropping cycle. We concluded that weed management strategies which influence soil moisture contents are likely to induce the most significant responses by the soil microflora.
No abstract is provided for this article.
Elevational gradients are increasingly recognized as a valuable tool for understanding how community and ecosystem properties respond to climatic factors, but little is known about how plant traits and their effects on ecosystem processes respond to elevation. We studied the response of plant leaf and litter traits, and litter decomposability across a gradient of elevation, and thus temperature, in subarctic tundra in northern Sweden for each of two contrasting vegetation types, heath and meadow, dominated by dwarf shrubs and herbaceous plants respectively. This was done at each of three levels; across species, within individual species, and the plant community using a community weighted average approach. Several leaf and litter traits shifted with increasing elevation in a manner consistent with greater conservation of nutrients at all three levels, and the most consistent response was an increase in tissue N to P ratio. However, litter decomposition was less directly responsive to elevation because the leaf and litter traits which were most responsive to elevation were not necessarily those responsible for driving decomposition. At the community level, the response to elevation of foliar and litter traits, and decomposability, varied greatly among the two vegetation types, highlighting the importance of vegetation type in determining ecological responses to climatic factors such as temperature. Finally our results highlight how understanding the responses of leaf and litter characteristics of functionally distinct vegetation types, and the processes that they drive, to temperature helps provide insights about how future climate change could affect tundra ecosystems.
Litter bags are often used to determine the impact of soil animals on litter decomposition rates through the use of varied mesh sizes that exclude soil animals on the basis of body size. However, concerns have been raised regarding confounding factors that can co-vary with mesh size (e.g., microclimatic differences and leaching losses) and that might affect mass loss from litter bags independent of soil animal effects. To explore if these factors may interfere with the interpretation of studies that have used litter bags of varying mesh sizes, we quantified the effects of mesh size (50 μm, 0.4 mm and 1.0 mm aperture) on litter mass loss in the absence of soil animals. Further we measured potential microclimate (temperatures, light transmission and moisture) differences that may co-vary with mesh size. In addition, we quantified litter mass losses through litter fragmentation and leaching. Litter mass loss in the absence of soil animals did not differ between mesh sizes, suggesting that the use of the different meshes does not generate confounding factors that directly influence mass loss rates in the absence of animals. Microclimatic differences between litter bags of different mesh sizes were minimal and revealed slightly warmer (0.7 °C) temperatures and easier water entry for the fine than the coarse mesh bags, but no effect on litter evaporation rates. Light transmittance was largest for the fine mesh (79%) compared to the medium (60%) and coarse mesh (73%). The impact of UV on litter mass loss was 1% higher in the coarse mesh. Loss of fragmented litter was considerably higher from the coarse mesh (93%) than the fine mesh bags (17%). In conclusion, different mesh sizes can be used to reliably quantify the role of soil animals in litter mass loss from litter bags. The greater litter mass loss from litter bags with coarser mesh sizes is however caused by the soil animals both promoting litter decomposition and greater litter fragmentation (with the undecomposed fragments then being lost from the bags). Additional approaches are needed to determine the relative importance of these two effects of soil animals on litter mass loss from litter bags.
No abstract is provided for this article.