Microbial and Faunal Interactions and Effects on Litter Nitrogen and Decomposition in Agroecosystems

We conducted field experiments to test the general hypothesis that the com- position of decomposer communities and their trophic interactions can influence patterns of plant litter decomposition and nitrogen dynamics in ecosystems. Conventional (CT) and no-tillage (NT) agroecosystems were used to test this idea because of their structural sim- plicity and known differences in their functional properties. Biocides were applied to ex- perimentally exclude bacteria, saprophytic fungi, and microarthropods in field exclosures. Abundances of decomposer organisms (bacteria, fungi, protozoa, nematodes, microar- thropods), decomposition rates, and nitrogen fluxes were quantified in surface and buried litterbags (Secale cereale litter) placed in both NT and CT systems. Measurements of in situ soil respiration rates were made concurrently. The abundance and biomass of all microbial and faunal groups were greater on buried than surface litter. The mesofauna contributed more to the total heterotrophic C in buried litter from CT (6-22%) than in surface litter from NT (0.4-1/1%). Buried litter decay rates (1.4-1.7%/d) were -2.5 times faster than rates for surface litter (0.5-O.7%/d). Ratios of fungal to bacterial biomass and fungivore to bacterivore biomass on NT surface litter generally increased over the study period resulting in ratios that were 2.7 and 2.2 times greater, respectively, than those of CT buried litter by the end of the summer. The exclusion experiments showed that fungi had a somewhat greater influence on the decomposition of surface litter from NT while bacteria were more important in the de- composition of buried litter from CT. The fungicide and bactericide reduced decomposition rates of NT surface litter by 36 and 25% of controls, respectively, while in CT buried litter they were reduced by 21 and 35% of controls, respectively. Microarthropods were more important in mobilizing surface litter nitrogen by grazing on fungi than in contributing to litter mass loss. Where fungivorous microarthropods were experimentally excluded, there was less than a 5% reduction in mass loss from litter of both NT and CT, but fungi- fungivore interactions were important in regulating litter N dynamics in NT surface litter. As fungal densities increased following the exclusion of microarthropods on NT surface litter, there was 25% greater N retention as compared to the control after 56 d of decay. Saprophytic fungi were responsible for as much as 86% of the net N immobilized (1.81 g /m2) in surface litter by the end of the study when densities of fungivorous microarthropods were low. Although bacteria were important in regulating buried litter decomposition rates and the population dynamics of bacterivorous fauna, their influence on buried litter N dynamics remains less clear. The larger microbial biomass and greater contribution of a bacterivorous fauna on buried litter is consistent with the greater carbon losses and lower carbon assimilation in CT than NT agroecosystems. In summary, our results suggest that litter placement can strongly influence the com- position of decomposer communities and that the resulting trophic relationships are im- portant to determining the rates and timing of plant litter decomposition and N dynamics. Furthermore, cross placement studies suggest that the decomposer communities within each tillage system, while not discrete, are adapted to the native litter placements in each.

[1]  D. Coleman,et al.  Reduction of microbial and faunal groups following application of streptomycin and captan in Georgia no-tillage agroecosystems , 1991 .

[2]  D. Coleman,et al.  Relationships between fungal and bacterial substrate-induced respiration, biomass and plant residue decomposition , 1991 .

[3]  J. Blair,et al.  Decay Rates, Nitrogen Fluxes, and Decomposer Communiies of Single‐ and Mixed‐Species Foliar Litter , 1990 .

[4]  K. Paustian,et al.  Ecology of arable land : organisms, carbon and nitrogen cycling , 1990 .

[5]  William L. Hargrove,et al.  A substrate-induced respiration (SIR) method for measurement of fungal and bacterial biomass on plant residues , 1990 .

[6]  D. Crossley,et al.  Soil mites in detrital food webs of conventional and no-tillage agroecosystems , 1990, Pedobiologia.

[7]  J. Blair,et al.  Effects of naphthalene on microbial activity and nitrogen pools in soil-litter microcosms , 1989 .

[8]  J. Blair,et al.  Resource quality and trophic responses to simulated throughfall: Effects on decomposition and nutrient flux in a no-tillage agroecosystem , 1989 .

[9]  J. Blair,et al.  Decomposition and nitrogen dynamics of surface weed residues in no-tillage agroecosystems under drought conditions: Influence of resource quality on the decomposer community , 1989 .

[10]  R. Kucey,et al.  EFFECT OF VESICULAR-ARBUSCULAR MYCORRHIZAL FUNGI AND CAPTAN ON GROWTH AND N2 FIXATION BY Rhizobium-INOCULATED FIELD BEANS , 1988 .

[11]  H. W. Hunt,et al.  Guilds or functional groups? An analysis of predatory arthropods from a shortgrass steppe soil , 1988, Pedobiologia.

[12]  J. Kough,et al.  DEPRESSED METABOLIC ACTIVITY OF VESICULAR-ARBUSCULAR MYCORRHIZAL FUNGI AFTER FUNGICIDE APPLICATIONS. , 1987, The New phytologist.

[13]  B. Sohlenius,et al.  LONG-TERM DYNAMICS OF NEMATODE COMMUNITIES IN ARABLE SOIL UNDER FOUR CROPPING SYSTEMS , 1987 .

[14]  D. Coleman,et al.  LITTER PLACEMENT EFFECTS ON MICROBIAL AND ORGANIC MATTER DYNAMICS IN AN AGROECOSYSTEM , 1987 .

[15]  D. Walter Trophic Behavior of "Mycophagous" Microarthropods , 1987 .

[16]  D. Coleman,et al.  Detritus Food Webs in Conventional and No-tillage Agroecosystems , 1986 .

[17]  D. E. Scott,et al.  Nitrogen Cycling as Affected by Interactions of Components in a Georgia Piedmont Agroecosystem , 1986 .

[18]  Bent Christensen,et al.  Barley straw decomposition under field conditions: Effect of placement and initial nitrogen content on weight loss and nitrogen dynamics , 1986 .

[19]  T. Fenchel The ecology of heterotrophic microflagellates , 1986 .

[20]  D. H. Knight,et al.  The nitrogen cycle in lodgepole pine forests, southeastern Wyoming , 1985 .

[21]  E. Ingham Review of the effects of 12 selected biocides on target and non-target soil organisms , 1985 .

[22]  David C. Coleman,et al.  Interactions of Bacteria, Fungi, and their Nematode Grazers: Effects on Nutrient Cycling and Plant Growth , 1985 .

[23]  H. Verhoef,et al.  Effects of collembolan grazing on nitrogen dynamics in a coniferous forest , 1985 .

[24]  K. Paustian Influence of fungal growth pattern on decomposition and nitrogen mineralization in a model system , 1985 .

[25]  S. Visser Role of the soil invertebrates in determining the composition of soil microbial communities , 1985 .

[26]  J. Laybourn-Parry A Functional Biology of Free-Living Protozoa , 1984 .

[27]  E. Odum,et al.  Nutrient budgets and internal cycling of N, P, K, Ca, and Mg in conventional tillage, no-tillage and old-field ecosystems on the Georgia piedmont , 1984 .

[28]  D. Crossley,et al.  Evaluation of Five Techniques for Recovering Postlarval Stages of Chiggers (Acarina: Trombiculidae) from Soil Habitats , 1984 .

[29]  W. Whitford,et al.  Carbon and Nitrogen Dynamics During the Decomposition of Litter and Roots of a Chihuahuan Desert Annual, Lepidium Lasiocarpum , 1984 .

[30]  G. W. Thomas,et al.  Changes in Soil Properties Under No-Tillage , 1984 .

[31]  B. Sohlenius,et al.  Colonization, population development and metabolic activity of nematodes in buried barley straw , 1984, Pedobiologia.

[32]  T. Seastedt The Role of Microarthropods in Decomposition and Mineralization Processes , 1984 .

[33]  D. A. Klein,et al.  Soil fungi: Relationships between hyphal activity and staining with fluorescein diacetate , 1984 .

[34]  K. Newell Interaction between two decomposer basidiomycetes and a collembolan under Sitka spruce: Grazing and its potential effects on fungal distribution and litter decomposition , 1984 .

[35]  J. Lagerlöf,et al.  Soil Fauna (Microarthropods, Enchytraeids, Nematodes) in Swedish Agricultural Cropping Systems , 1983 .

[36]  Lars R. Bakken,et al.  Buoyant Densities and Dry-Matter Contents of Microorganisms: Conversion of a Measured Biovolume into Biomass , 1983, Applied and environmental microbiology.

[37]  T. Seastedt,et al.  Nutrients in forest litter treated with naphthalene and simulated throughfall: A field microcosm study , 1983 .

[38]  D. Coleman,et al.  Short-term bacterial growth, nutrient uptake, and ATP turnover in sterilized, inoculated and C-amended soil: The influence of N availability , 1983 .

[39]  C. Reid,et al.  Biological Strategies of Nutrient Cycling in Soil Systems , 1983 .

[40]  H. Petersen,et al.  A comparative analysis of soil fauna populations and their role in decomposition processes , 1982 .

[41]  D. A. Klein,et al.  Relationship between fluorescein diacetate-stained hyphae and oxygen utilization, glucose utilization, and biomass of submerged fungal batch cultures , 1982, Applied and environmental microbiology.

[42]  T. Fenchel Ecology of heterotrophic microflagellates. II Bioenergetics and growth , 1982 .

[43]  W. Whitford,et al.  The Effects of Microarthropods on Litter Decomposition in a Chihuahuan Desert Ecosystem , 1981 .

[44]  W. Whitford,et al.  THE ROLE OF MITES AND NEMATODES IN EARLY STAGES OF BURIED LITTER DECOMPOSITION IN A DESERT , 1981 .

[45]  R. Hanlon Influence of grazing by Collembola on the activity of senescent fungal colonies grown on media of different nutrient concentration , 1981 .

[46]  James P. Martin,et al.  Incorporation of a Wide Variety of Organic Substrate Carbons into Soil Biomass as Estimated by the Fumigation Procedure 1 , 1981 .

[47]  D. M. Griffin,et al.  Water and Microbial Stress , 1981 .

[48]  D. Coleman,et al.  Habitable pore space and microbial trophic interactions , 1980 .

[49]  J. Doran Soil microbial and biochemical changes associated with reduced tillage. , 1980 .

[50]  J. F. McBrayer,et al.  Effect of snow-pack on oak-litter breakdown and nutrient release in a Minnesota forest. , 1980 .

[51]  Björn Sohlenius,et al.  Abundance, biomass and contribution to energy flow by soil nematodes in terrestrial ecosystems , 1980 .

[52]  J. Stout The Role of Protozoa in Nutrient Cycling and Energy Flow , 1980 .

[53]  J. Anderson,et al.  Decomposition in Terrestrial Ecosystems , 1979 .

[54]  E. Paul,et al.  Conversion of Biovolume Measurements of Soil Organisms, Grown Under Various Moisture Tensions, to Biomass and Their Nutrient Content , 1979, Applied and environmental microbiology.

[55]  D. Coleman,et al.  The use of soil microcosms in evaluating bacteriophagic nematode responses to other organisms and effects on nutrient cycling , 1979 .

[56]  D. Coleman,et al.  THE INFLUENCE OF AMOEBAE ON THE UPTAKE OF NITROGEN BY PLANTS IN GNOTOBIOTIC SOIL , 1979 .

[57]  Anthony William Aldridge Brown,et al.  Ecology of pesticides , 1979 .

[58]  J. Oades,et al.  Utilization of organic materials in soil aggregates by bacteria and fungi , 1978 .

[59]  M. Bertoldi,et al.  Effects of benomyl and captan on rhizosphere fungi and the growth of Allium cepa , 1978 .

[60]  B. Söderström Vital staining of fungi in pure cultures and in soil with fluorescein diacetate , 1977 .

[61]  D. Parkinson,et al.  Effects of collembolan grazing on fungal colonization of leaf litter , 1977 .

[62]  David C. Coleman,et al.  Compartmental Analysis of "Total Soil Respiration": An Exploratory Study , 1973 .

[63]  L. Babiuk,et al.  The use of fluorescein isothiocyanate in the determination of the bacterial biomass of grassland soil. , 1970, Canadian journal of microbiology.

[64]  A. Cockburn,et al.  Studies on the growth and feeding of Tetrahymena pyriformis in axenic and monoxenic culture. , 1968, Journal of general microbiology.

[65]  M. Witkamp,et al.  The Role of Arthropods and Microflora in Breakdown of White Oak Litter , 1966, Pedobiologia.

[66]  J. Olson,et al.  Energy Storage and the Balance of Producers and Decomposers in Ecological Systems , 1963 .

[67]  M. H. Quenouille,et al.  A Technique for the Quantitative Estimation of Soil Micro-organisms: With a Statistical Note by , 1948 .

[68]  B. Singh A method of estimating the numbers of soil protozoa, especially amoebae, based on their differential feeding on bacteria. , 1946, The Annals of applied biology.