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Forest floor-mineral soil interactions in the internal nitrogen cycle of an old-growth forest

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Abstract

Seasonal patterns and annual rates of N inputs, outputs, and internal cycling were determined for an old-growth mixed-conifer forest floor in the Sierra Nevada Mountains of California. Rates of net N mineralization within the forest floor, and plant N-uptake and leaching of inorganic N from the forest floor were 13, 10, and 9 kg-N ha-1 yr-1, respectively. The Mediterranean-type climate appeared to have a significant effect on N cycling within this forest, such that all N-process and flow rates showed distrinct seasonal patterns. We estimated the forest floor supplies less than one-third of the total aboveground plant N-uptake in this forest. The rate of net nitrification within the forest floor was always low (1 kg-NO3 --N ha-1 30d-1). Mean residence times for organic matter and N in the forest floor were 13 and 34 years, respectively, suggesting that this forest floor layer is a site of net N immobilization within this ecosystem. We examined the influence of the forest floor on mineral soil N dynamics by injecting small amounts of15N-enriched (NH4)2SO4 solutions into the surface mineral soil with the forest floor present (+FF) or removed (-FF). K2SO4-extractable NO3 --N, total inorganic-N, and total-N pool sizes in the mineral soil were initially increased after forest floor removal (after 4 months), but NO3 --N and total inorganic-N were not significantly different thereafter. Microbial biomass-N and K2SO4-extractable total-N pool sizes were also found to be larger in mineral soils without a forest floor after 1 and 1.3 years, respectively. Total15N-recovery was greater in the +FF treatment compared to the -FF treatment after 1-year (about 50% and 35%, respectively) but did not differ after 1.3 years (both about 35%), suggesting that the forest floor delays but does not prevent the N-loss from the surface mineral soil of this forest. We estimated using our15N data that fungal translocation from the mineral soil to the forest floor may be as large as 9 kg-N ha-1 yr-1 (similar in magnitude to other N flows in this forest), and may account for all of the observed absolute increase of N in litter during the early stages of decomposition at this site. Our results suggest that the forest floor acts both as a source and sink for N in the mineral soil.

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References

  • Adams MA, Polglase PJ, Attiwill PM & Weston CJ (1989) In situ studies of nitrogen mineralizaiton and uptake in forest soils: some comments on methodology. Soil Biology and Biochemistry 21: 423–429

    Google Scholar 

  • Berg B & Söderström B (1979) Fungal biomass and nitrogen in decomposing Scots pine needle litter. Biology and Biochemistry 11: 339–341

    Google Scholar 

  • Binkley D & Hart SC (1989) The components of nitrogen availability assessments in forest soils. Advances in Soil Science 10: 57–112

    Google Scholar 

  • Bocock KL (1963) Changes in the amount of nitrogen in decomposing leaf letter in sessile oak (Quercus petraea). Journal of Ecology 51: 555–556

    Google Scholar 

  • Bremner JM & Mulvaney CS (1982) Nitrogen — Total In: Page AL, Miller RH & Keeney DR (Eds) Methods of Soil Analysis, Part 2, Chemical and Microbiological Properties (pp 595–624). Second Edn. American Society of Agronomy, Madison, Wisconsin

    Google Scholar 

  • Bringmark L (1980) Ion leaching through a podsol in a Scots pine stand. In: Persson T (Ed) Structure and Function of Northern Coniferous Forests — An Ecosystem Study. Ecological Bulletins (Stockholm) 32: 341–361

  • Brookes PC, Landman A, Pruden G & Jenkinson DS (1985) Chloroform fumigation and the release of soil nitrogen: a rapid direct extraction method to measure microbial biomass nitrogen in soil. Soil Biology and Biochemistry 17: 837–842

    Google Scholar 

  • Brooks PD, Stark JM, McInteer BB & Preston T (1989) A diffusion method to prepare soil extracts for automated Nitrogen-15 analysis. Soil Science Society of American Journal 53: 1707–1711

    Google Scholar 

  • Cole DW (1981) Nitrogen uptake and translocation by forest ecosystems. Ecological Bulletins (Stockholm) 33: 219–232

    Google Scholar 

  • Cole DW & Rapp M (1981) Elemental cycling in forest ecosystems. In: Reiche DE (Ed) Dynamic Properties of Forest Ecosystems (pp 341–409). International Biological Program, 23

  • Davidson EA, Eckert RW, Hart SC & Firestone MK (1989) Direct extraction of microbial biomass nitrogen from forest and grassland soils of California. Soil Biology and Biochemistry 21: 773–778

    Google Scholar 

  • Davidson EA, Hart SC & Firestone MK (submitted) Nitrate is important in the internal nitrogen cycle of a mature coniferous forest. Ecology

  • DiStefano Jf & Gholz HL (1986) A proposed use of ion exchange resins to measure nitrogen mineralization and nitrification in intact soil cores. Communications in Soil Science and Plant Analysis 17: 989–998

    Google Scholar 

  • Dyck WJ, Mees CA & Hodgkiss PD (1987) Nitrogen availability and comparison of uptake in two New Zealand Pinus radiata forests. New Zealand Journal of Forestry Science 17: 338–352

    Google Scholar 

  • Ellenberg VH (1977) Stickstoff als Standortsfaktor, insbesondere fr Mitteleuropeische Pflanzengesellschaften. Oecologia Plantarum 12: 1–22

    Google Scholar 

  • Eno CH (1960) Nitrate production in the field by incubating the soil in polyethylene bags. Soil Science Society of American Proceeding 24: 277–279

    Google Scholar 

  • Fahey TL, Yavitt JB, Peasson JA & Knight DH (1985) The nitrogen cycle in lodgepole pine forests, southeastern Wyoming. Biogeochemistry 1: 257–275

    Google Scholar 

  • Gessel SP, Cole DW & Steinbrenner EC (1973) Nitrogen balances in forest ecosystems of the pacific northwest. Soil Biology and Biochemistry 5: 19–34

    Google Scholar 

  • Gosz JR, Likens GE & Bormann FH (1973) Nutrient releases from decomposing leaf and branch litter in the Bubbard Brook Forest, New Hampshire, Ecological Monographs 43: 173–191

    Google Scholar 

  • Granhall U & Lindberg T (1977) Nitrogen fixation at coniferous forest sites within the Swecon project. Swedish Coniferous Forest Project Technical report 11: 1–39

    Google Scholar 

  • Grier CC, Vogt KA, Keyes MR & Edmonds RL (1981) Biomass distribution and aboveand belowground production in young and mature Abies amabilis zone ecosystems of the Washington Cascades. Canadian Journal of Forest Research 11: 155–167

    Google Scholar 

  • Hart SC (1990) Control of decomposition processes and nutrient flow in a California forest and grassland. Unpublished Ph.D. Dissertation, University of California, Berkeley

  • Hart SC & Binkley D (1984) Colorimetric interference and recovery of adsorbed ions from ion exchange resins. Communications in Soil Science and Plant Analysis 15: 893–902

    Google Scholar 

  • Hart SC & Firestone MK (1989) Evaluation of three in situ soil nitrogen availability assays. Canadian Journal of Forest Research 19: 185–191

    Google Scholar 

  • Hart SC & Gunther AJ (1989) In situ estimates of annual net nitrogen mineralization and nitrification in a subarctic watershed. Oecologia 80: 284–288

    Google Scholar 

  • Jackson LE, Schimel JP & Fireston MK (1989) Short-term partitioning of ammonium and nitrate between plants and microbes in an annual grassland. Soil Biology and Biochemistry 21: 409–415

    Google Scholar 

  • Jackson LE, Strauss RB, Fireston MK & Bartolome JW (1988) Plant and soil nitrogen dynamics in California annual grassland. Plant and Soil 110: 9–17

    Google Scholar 

  • Jorgensen JR, Wells CG & Metz LZ (1980) Nutrient changes in decomposing loblolly pine forest floors. Soil Science Society of America Journal 44: 1307–1314

    Google Scholar 

  • Keeney DR and Nelson DW (1982) Nitrogen — inorganic forms. In: Page AL, Miller RH & Keeney DR (Eds) Methods of Soil Analysis, Part 2, Chemical and Microbiological Properties (pp 643–698). Second Edn. American Society of Agronomy, Madison, Wisconsin

    Google Scholar 

  • Lamont BB (1983) Strategies for maximizing nutrient uptake in two Mediterranean ecosystems of low nutrient status. In: Kruger FJ, Mitchell DT & Jarvis JUM (Eds) Mediterranean-Type Ecosystems — The Role of Nutrients (pp 246–273). Ecological Studies 43, Springer-Verlag, Berlin

    Google Scholar 

  • Nadelhoffer KJ, Aber JD & Melillo JM (1983) Leaf litter production and soil organic matter dynamics along a nitrogen-availability gradient in Southern Wisconsin. Canadian Journal of Forest Research 13: 12–21

    Google Scholar 

  • Nadelhoffer KJ, Aber JD & Melillo JM (1984) Seasonal patterns of ammonium and nitrate uptake in nine temperate forest ecosystems. Plant and Soil 80: 321–335

    Google Scholar 

  • Nadelhoffer KJ, Aber JD & Melillo JM (1985) Fine roots, net primary production, and soil nitrogen availability: a new hypothesis. Ecology 66: 1377–1390

    Google Scholar 

  • Olson JS (1963) Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44: 322–331

    Google Scholar 

  • Pastor J, Aber JD, McClaugherty CA & Melillo JM (1984) Aboveground production and N and P cycling along a nitrogen mineralization gradient on Blackhawk Island, Wisconsin. Ecology 65: 256–268

    Google Scholar 

  • Powers RF (1990) Soil nitrogen mineralization along an altitudinal gradient: interactions of soil temperature, moisture, and substrate quality. Forest Ecology and Management 30: 19–29

    Google Scholar 

  • QuikChem Systems (1986) QuikChem method no. 12-107-06-1-A. Quikchem Systems, division of Lachat Chemicals, Inc., Mequon, Wisconsin

    Google Scholar 

  • QuikChem Systems (1987) QuikChem method no. 12-107-04-1-A. Quikchem Systems, division of Lachat Chemicals, Inc., Mequon, Wisconsin

    Google Scholar 

  • Schimel JP & Firestone MK (1989) Nitrogen incorporation and flow through a coniferous forest soil profile. Soil Science Society of America Journal 53: 779–784

    Google Scholar 

  • Schimel JP, Jackson LE & Firestone MK (1989) Spatial and temporal effects on plantmicrobial competition for inorganic nitrogen in a California annual grassland. Soil Biology and Biochemistry 21: 1059–1066

    Google Scholar 

  • Smethurst PJ & Nambiar EKS (1989) An appraisal of the in situ soil-core technique for measuring nitrogen uptake by a young Pinus radiata plantation. Soil Biology and Biochemistry 21: 939–942

    Google Scholar 

  • Sollins P & McCorison FM (1981) Nitrogen and carbon solution chemistry of an old growth coniferous forest watershed before and after cutting. Water Resources Research 17: 1409–1418

    Google Scholar 

  • Staaf H & Berg B (1977) Mobilization of plant nutrients in a Scots pine forest mor in Central Sweden. Silva Fennica 11: 210–217

    Google Scholar 

  • Steel RGD & Torrie JH (1980) Principles and Procedures of Statistics, 2nd edition. McGraw-Hill, New York, 633 pp

    Google Scholar 

  • STSC, Inc. (1986) Statgraphics user's guide. STSC Inc., Rockville, MD

    Google Scholar 

  • Vogt, KA, Grier CC, Meier CE & Keyes MR (1983) Organic matter production and nutrient dynamics in forest floors of young and mature Abies amabilis stands in western Washington, as affected by fine-root input. Ecological Monographs 53: 139–157

    Google Scholar 

  • Vogt KA, Grier CC & Vogt DJ (1986) Production, turnover, and nutrient dynamics of above- and belowground detritus of world forests. Advances in Ecological Research 15: 303–377

    Google Scholar 

  • Waring RH & Schlesinger WH (1985) Decomposition and forest soil development. In: Forest Ecosystems: Concepts and Management (pp 181–210). Academic Press, Inc., NY

    Google Scholar 

  • Weber MG & Van Cleve K (1981) Nitrogen dynamics in the forest floor of interior Alaska black spruce ecosystems. Canadian Journal of Forest Research 11: 743–751

    Google Scholar 

  • Weber MG & Van Cleve K (1984) Nitrogen transformations in feather moss and forest floor layers of interior Alaska black spruce ecosystems. Canadian Journal of Forest Research 14: 278–290

    Google Scholar 

  • Wells C & Jorgensen JR (1975) Nutrient cycling in loblolly pine plantations. In: Bernier B & Winget CH (Eds) Forest Soils and Forest Land Management (pp 137–158). Les Presses de L'Universite Laval, Quebec

    Google Scholar 

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Hart, S.C., Firestone, M.K. Forest floor-mineral soil interactions in the internal nitrogen cycle of an old-growth forest. Biogeochemistry 12, 103–127 (1991). https://doi.org/10.1007/BF00001809

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