Search results for "Soil food web"
showing 10 items of 10 documents
Responses of decomposer community to root-isolation and addition of slash
2001
Abstract We studied the causal relationships between forest harvesting and the soil decomposer community focusing on suppression of energy inputs from trees to the soil through root–mycorrhizal network and increased energy input to the soil in the form of slash left on site. We hypothesised that both of these factors would affect the decomposer community, since the soil food web has been regarded as a system in which the amount of resources controls the numbers of consumers. To study the importance of these factors without changes in microclimate, like in sunshine and shade, taking place in clear-felled areas, the experiment was performed in a mature spruce ( Picea abies (L.) Karst.) forest…
Effects of microbivore species composition and basal resource enrichment on trophic-level biomasses in an experimental microbial-based soil food web.
1998
Previous theoretical and empirical evidence suggests that species composition within trophic levels may profoundly affect the response of trophic-level biomasses to enhanced basal resources. To test whether species composition of microbivorous nematodes has such an effect in microbial-based soil food webs, I created three microcosm food webs, consisting of bacteria, fungi, bacterial-feeding nematodes (Acrobeloides tricornus, Caenorhabditis elegans), fungal-feeding nematodes (Aphelenchus avenae, Aphelenchoides sp.) and a predatory nematode (Prionchulus punctatus). The food webs differed in species composition at the second trophic level: food web A included A. tricornus and Aph. avenae, food…
No evidence of trophic cascades in an experimental microbial-based soil food web
1998
Trophic-dynamic theories predict the biomass and productivity of trophic levels to be partially top-down regulated in food webs, and that the top-down regulation will manifest itself as cascading trophic interactions. We tested the two principal predictions deduced from these theories: trophic cascades of (1) biomass regulation and (2) productivity regulation occur in food webs. We created three food webs with either one, two, or three trophic levels in soil microcosms containing a sterilized mixture of leaf litter and humus. Twenty species of bacteria and fungi formed the first trophic level, a bacterivorous nematode (Caenorhabditis elegans) and a fungivorous nematode (Aphelenchoides sp.) …
Responses of microbial-feeding nematodes to organic matter distribution and predation in experimental soil habitat
2001
Abstract Soils are spatially heterogeneous environments, a condition which is likely to affect the structure and function of soil food webs. To study the influence of soil organic matter distribution on decomposer food webs, we established microcosms that contained either: (1) large patches of initially sterile humus-litter mixture placed within sterile sand matrix (creating a large-patch habitat; LPH); or (2) blend of sand and humus-litter mixture (creating a small-patch habitat; SPH). Ten species of bacteria and ten species of fungi, and two bacterial-feeding ( Acrobeloides tricornis , Caenorhabditis elegans ) and two fungal-feeding ( Aphelenchus avenae , Aphelenchoides sp.) nematodes wer…
Does plant growth phase determine the response of plants and soil organisms to defoliation?
2005
Abstract To test a hypothesis that the effects of defoliation on plant ecophysiology and soil organisms depend on the timing of defoliation within a growing season, we established a greenhouse experiment using replicated grassland microcosms. Each microcosms was composed of three plant species, Trifolium repens , Plantago lanceolata and Phleum pratense , growing in grassland soil with a diverse soil community. The experiment consisted of two treatment factors—defoliation and plant growth phase (PGP)—in a fully factorial design. Defoliation had two categories, i.e. no trimming or trimming a total of four times at 2 week intervals. The PGP treatment had four categories, i.e. 1, 3, 7 or 13 wee…
Priorities for research in soil ecology
2017
The ecological interactions that occur in and with soil are of consequence in many ecosystems on the planet. These interactions provide numerous essential ecosystem services, and the sustainable management of soils has attracted increasing scientific and public attention. Although soil ecology emerged as an independent field of research many decades ago, and we have gained important insights into the functioning of soils, there still are fundamental aspects that need to be better understood to ensure that the ecosystem services that soils provide are not lost and that soils can be used in a sustainable way. In this perspectives paper, we highlight some of the major knowledge gaps that shoul…
Belowground responses by AM fungi and animal trophic groups to repeated defoliation in an experimental grassland community
2005
Abstract We tested a hypothesis that the effects of defoliation on plants and soil organisms vary with the number of successive defoliations. We established a 23-week greenhouse experiment using replicated grassland microcosms that were composed of three plant species, Trifolium repens , Plantago lanceolata and Phleum pratense , growing together in grassland soil with a diverse soil community. The experiment consisted of two treatment factors-defoliation and harvest time-in a fully factorial design. The defoliation treatment had two levels, i.e. no trimming and trimming of plants every 2 weeks, and the harvest time five levels, i.e. harvests after 1–3, 5 and 7 trimmings. Shoot production (t…
Spot mounding and granulated wood ash increase inorganic N availability and alter key components of the soil food web in clear-cut Norway spruce fore…
2012
Abstract The interactive effects of site preparation (spot mounding) and fertilization (granulated wood ash) on soil properties, soil micro- and mesofauna and ground vegetation were studied in two Norway spruce plantations established in clear-cut forests in Central Finland. Half of the seedlings were planted on mounds created by the planting machine, and the rest on intact forest floor. Half of the seedlings on mounded and intact forest floor were fertilized by adding granulated wood ash to circular plots surrounding the seedlings. Initial samples were taken from mounded and intact soil immediately after planting in June. Samples were taken from all treated plots in the autumn in the first…
Role of Soil Organisms in the Maintenance of Species-Rich Seminatural Grasslands through Mowing
2009
To preserve species-rich grasslands, management practices such as mowing are often required. Mowing is known to promote aboveground conditions that help to maintain plant species richness, but whether belowground effects are important as well is not known. We hypothesized that if mowing decreases belowground carbon transfer by reducing root mass, this will reduce the abundance and activity of soil decomposers and lead to diminished nutrient availability in soil. In grasslands, this would provide a means to mitigate the negative effects of nitrogen enrichment on plant species richness. We established experimental plots on grassland with one-third of plots growing untouched, one-third mowed o…
Interplay of omnivory, energy channels and C availability in a microbial-based soil food web
1998
To study the effects of omnivory on the structure and function of soil food webs and on the control of trophic-level biomasses in soil, two food webs were established in microcosms. The first one contained fungi, bacteria, a fungivorous nematode (Aphelenchoides saprophilus) and a bacterivorous nematode (Caenorhabditis elegans), and the second one fungi, bacteria, the fungivore and an omnivorous nematode (Mesodiplogaster sp.) feeding on both bacteria and the fungivore. Half of the replicates of each food web received additional glucose. The microcosms were sampled destructively at 5, 9, 13 and 19 weeks to estimate the biomass of microbes and nematodes and the soil NH4+-N concentration. The e…