Plant and Soil

, Volume 187, Issue 2, pp 159–219 | Cite as

Review of root dynamics in forest ecosystems grouped by climate, climatic forest type and species

  • Kristiina A. Vogt
  • Daniel J. Vogt
  • Peter A. Palmiotto
  • Paul Boon
  • Jennifer O'Hara
  • Heidi Asbjornsen
Carbon Allocation Mechanisms and Controls Carbon Allocation Within Plants


Patterns of both above- and belowground biomass and production were evaluated using published information from 200 individual data-sets. Data sets were comprised of the following types of information: organic matter storage in living and dead biomass (e.g. surface organic horizons and soil organic matter accumulations), above- and belowground net primary production (NPP) and biomass, litter transfers, climatic data (i.e. precipitation and temperature), and nutrient storage (N, P, Ca, K) in above- and belowground biomass, soil organic matter and litter transfers. Forests were grouped by climate, foliage life-span, species and soil order. Several climatic and nutrient variables were regressed against fine root biomass or net primary production to determine what variables were most useful in predicting their dynamics. There were no significant or consistent patterns for above- and belowground biomass accumulation or NPP change across the different climatic forest types and by soil order. Similarly, there were no consistent patterns of soil organic matter (SOM) accumulation by climatic forest type but SOM varied significantly by soil order—the chemistry of the soil was more important in determining the amount of organic matter accumulation than climate. Soil orders which were high in aluminum, iron, and clay (e.g. Ultisols, Oxisols) had high total living and dead organic matter accumulations-especially in the cold temperate zone and in the tropics. Climatic variables and nutrient storage pools (i.e. in the forest floor) successfully predicted fine root NPP but not fine root biomass which was better predicted by nutrients in litterfall. The importance of grouping information by species based on their adaptive strategies for water and nutrient-use is suggested by the data. Some species groups did not appear to be sensitive to large changes in either climatic or nutrient variables while for others these variables explained a large proportion of the variation in fine root biomass and/or NPP.

Key words

above- and belowground biomass and production above- and belowground litter transfers boreal forests climatic variables cold and warm temperate forests forest floor accumulations nutrients soil organic matter subtropical and tropical forests 


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  1. Aber, J D, Melillo, J M, Nadelhoffer, K J, McClaugherty, C A and Pastor, J 1985 Fine root turnover in forest ecosystems in relation to quantity and form of nitrogen availability: a comparison of two methods. Oecologia 66, 317–321.Google Scholar
  2. Aber, J D and Federer, C A 1992 A generalized, lumped-parameter model of photosynthesis, evapotranspiration and net primary production in temperate and boreal forest ecosystems. Oecologia 92, 463–474.CrossRefGoogle Scholar
  3. Abrams, M D and Kubiske, M E 1990 Leaf structural characteristics of 31 hardwood and conifer tree species in central Wisconsin: influence of light regime and shade tolerance rank. For. Ecol. Manage. 31, 245–254.Google Scholar
  4. Aerts, R 1995 The advantages of being evergreen. Trends Ecol. Evol 10, 402–407.CrossRefGoogle Scholar
  5. Alexander, I J and Fairley, R I 1983 Effects of N fertilization on populations of fine roots and mycorrhizas in spruce humus. Plant and Soil 71, 49–53.Google Scholar
  6. Anderson, J M 1991 The effects of climate change on decomposition processes in grassland and coniferous forests. Ecol. Appl. 1, 326–347.Google Scholar
  7. Arthur, M A and Fahey, T J 1992 Biomass and nutrients in an Engelmann spruce-subalpine fir forest in north central Colorado: pools, annual production, and internal cycling. Can. J. For. Res. 22, 315–325.Google Scholar
  8. Axelsson B and Brakenhielm S 1980 Investigation sites of the Swedish Coniferous Forest project-biological and physiographical features. In Structure and Function of Northern Coniferous Forests—an Ecosystem Study. Ed. T Persson. Ecol. Bull. 32, 25–64.Google Scholar
  9. Bazzaz, F A, Chiariello, N R, Coley, P D and Pitelka, L F 1987 Allocating resources to reproduction and defense. BioSci. 37, 58–67.Google Scholar
  10. Benzing, D H 1991 Aerial roots and their environments. In Plant Roots. The Hidden Half. Eds. YWiasel, AEshel and UKafkafi. pp 867–886. Marcel Dekler, Inc. New York, USA.Google Scholar
  11. Berish, C W 1982 Root biomass and surface area in three successional tropical forests. Can. J. For. Res. 12, 699–704.Google Scholar
  12. Bloomfield, J, Vogt, K A and Vogt, D J 1993 Decay rate and substrate quality of fine roots and foliage of two tropical tree species in the Luquillo Experimental Forest, Puerto Rico. Plant and Soil 150, 233–245.Google Scholar
  13. Blyth, J R and MacLeod, D A 1981 Sitka spruce (Picea sitchensis) in northeast Scotland. I. Relationships between site factors and growth. Forestry 54, 41–62.Google Scholar
  14. Bormann, F H and Likens, G E 1979 Pattern and Process in a Forested Ecosystem. Springer-Verlag, New York, USA.Google Scholar
  15. Boudot, J P, Bel Hadj, B A and Chone, T 1986 Carbon mineralization in andosols and aluminum rich highland soils. Soil Biol. Biochem. 18, 457–461.CrossRefGoogle Scholar
  16. Brown, S and Lugo, A E 1982 The storage and production of organic matter in tropical forests and their role in the global carbon cycle. Biotropica 14, 161–187.Google Scholar
  17. Burke, M K and Raynal, D J 1995 Fine root growth phenology, production, and turnover in a northern hardwood forest ecosystem. Plant and Soil 162, 135–146.Google Scholar
  18. Cabanettes A 1979 Croissance, biomasse et productivité de Pinus pinea L. en petite Camargue. Unpublished Ph.D. Dissertation. Academié de Montpellier, Université des Sciences et Techniques du Languedoc, Montpellier, France.Google Scholar
  19. Cannell, M G R 1982 World Forest Biomass and Primary Production Data. Academic Press, London, UK.Google Scholar
  20. Cannell, M G R and Dewar, R C 1994 Carbon allocation in trees: a review of concepts for modelling. Adv. Ecol. Res. 25, 59–105.Google Scholar
  21. Carey, M L and Farrell, E P 1978 Production, accumulation and nutrient content of Sitka spruce litterfall. Ir. For. 35, 35–44.Google Scholar
  22. Castellanos, J, Maass, M and Kummerow, J 1991 Root biomass of a dry deciduous tropical forest in Mexico. Plant and Soil 131, 225–228.Google Scholar
  23. Cavelier, J 1992 Fine-root biomass and soil properties in a semideciduous and a lower montane rain forest in Panama. Plant and Soil 142, 187–201.Google Scholar
  24. Chapin, F SIII 1991 Integrated responses of plants to stress. BioSci. 41, 29–36.Google Scholar
  25. Chapin, F SIII and Kedrowski, R A 1983 Seasonal changes in nitrogen and phosphorous fractions and autumn retranslocations in evergreen and deciduous taiga trees. Ecology 64, 376–391.Google Scholar
  26. Chapin, F SIII, Bloom, A J, Field, C B and Waring, R H 1987 Plant responses to multiple environmental factors. BioSci. 37, 49–57.Google Scholar
  27. Climates of the States 1980 National Oceanic and Atmospheric Administration Narrative Summaries, Tables, and Maps for Each State. 2nd ed. Vols. 1 and 2. Gale Research, Book Tower, Detroit, Michigan, USA.Google Scholar
  28. Cole D W and Gessel S P 1968 Cedar River Research. A Program for Studying the Pathways, Rates, and Processes of Elemental Cycling in a Forest Ecosystem. Forest Resources Monograph. Institute of Forest Products, University of Washington College of Forest Resources Contribution No 4. 54 p.Google Scholar
  29. Cole, D W and Rapp, M 1981 Elemental cycling in forests. In Dynamic Properties of Forest Ecosystems. International Biological Programme 23. Ed. D EReichle. pp 341–409. Cambridge University Press, London, UK.Google Scholar
  30. Coleman D C, Oades J M and Uehara G (eds) 1989 Dynamics of Soil Organic Matter in Tropical Ecosystems. NifTAL Project. Department of Agronomy and Soil Science, College of Trop. Agric. and Human Resources, University of Hawaii.Google Scholar
  31. Coley, P D 1988 Effects of plant growth rate and leaf lifetime on the amount and type of anti-herbivore defense. Oecologia 74, 531–536.Google Scholar
  32. Comeau, P G and Kimmins, J P 1989 Above- and below-ground biomass and production of lodgepole pine on sites with differing soil moisture regimes. Can. J. For. Res. 19, 447–454.Google Scholar
  33. Covington W W 1976 Forest floor organic matter and nutrient content and leaffall during secondary succession in Northern hardwoods. Ph D Dissertation. Yale University, New Haven, CT, USA.Google Scholar
  34. Covington, W W 1981 Changes in forest floor organic matter and nutrient content following clear cutting in northern hardwoods. Ecology 62, 41–48.Google Scholar
  35. Cox, T L, Harris, T L, Ausmus, B S and Edwards, N T 1978 The role of roots in biogeochemical cycles in an eastern deciduous forest. Pedobiologica 18, 264–271.Google Scholar
  36. Cromack K Jr 1973 Litter production and decomposition in a mixed hardwood watershed and a white pine watershed at Coweeta Hydrologic Station, North Carolina. Unpublished PhD Dissertation. University of Georgia, Athens, Georgia, USA.Google Scholar
  37. Cuevas, E and Medina, E 1986 Nutrient dynamics within Amazonian forest ecosystems. I. Nutrient flux in fine litter fall and efficiency of nutrient utilization. Oecologia 68, 466–472.Google Scholar
  38. Cuevas, E and Medina, E 1988 Nutrient dynamics within Amazonian forests. II. Fine root growth, nutrient availability and leaf litter decomposition. Oecologia 76, 222–235.Google Scholar
  39. Cuevas, E, Brown, S and Lugo, A E 1991 Above- and belowground organic matter storage and production in a tropical pine plantation and a paired broadleaf secondary forest. Plant and Soil 135, 257–268.Google Scholar
  40. Dahlgren, R A, Vogt, K A and Ugolini, F C 1991 The influence of soil chemistry on fine root aluminum concentrations in a subalpine Spodosol, Washington, USA. Plant and Soil 133 117–129.Google Scholar
  41. Day, F PJr 1982 Litter decomposition rates in the seasonally flooded Great Dismal Swamp. Ecology 63, 670–678.Google Scholar
  42. Day, F PJr 1984 Biomass and litter accumulation in the Great Dismal Swamp. In Cypress Swamps. Eds. K CEwel and H TOdum. pp 386–392. University Florida Press Gainesville, Florida, USA.Google Scholar
  43. DeAngelis, D L, Gardner, R H and Shugart, H H 1981 Productivity of forest ecosystems studied during the IBP: The woodlands data set. In Dyr mic Properties of Forest Ecosystems. International Biological Programme 23. Ed. D EReichle. pp 567–672. Cambridge University Press, London, UK.Google Scholar
  44. Deans, J D 1979 Fluctuations of the soil environment and fine root growth in a young Sitka spruce plantation. Plant and Soil 52, 195–208.Google Scholar
  45. Deans, J D 1981 Dynamics of coarse root production in a young plantation of Picea sitchensis. Forestry 54, 139–155.Google Scholar
  46. Edwards, P J 1977 Studies of mineral cycling in a montane rainforest in New Guinea. II. The production and disappearance of litter. J. Ecol. 65, 971–992.Google Scholar
  47. Edwards, P J 1982 Studies of mineral cycling in a montane rainforest in New Guinea. V. Rates of cycling in throughfall and litterfall. J. Ecol. 70, 807–827.Google Scholar
  48. Edwards, P J and Grubb, P J 1977 Studies of mineral cycling in a montane rainforest in New Guinea. I. The distribution of organic matter in the vegetation and soil. J. Ecol. 65, 943–969.Google Scholar
  49. Edwards, P J and Grubb, P J 1982 Studies of mineral cycling in a montane rainforest in New Guinea. IV. Soil characteristics and the division of mineral elements between the vegetation and soil. J. Ecol. 70, 649–666.Google Scholar
  50. Egunjobi, J K and Bada, S O 1979 Biomass and nutrient distribution in stands of Pinus caribaea L. in the dry forest zone of Nigeria. Biotropica 11, 130–135.Google Scholar
  51. Ewel, J J 1976 Litterfall and leaf decomposition in a tropical forest succession in eastern Guatemala. J. Ecol. 64, 293–308.Google Scholar
  52. Ewel, K C, Cropper, W PJr and Gholz, H L 1987a Soil CO2 evolution in Florida slash pine plantations. I. Changes through time. Can. J. For. Res. 17, 325–329.Google Scholar
  53. Ewel, K C, Cropper, W PJr and Gholz, H L 1987b Soil CO2 evolution in Florida slash pine plantations. II. Importance of root respiration. Can. J. For. Res. 17, 330–333.Google Scholar
  54. Fahey, T J and Hughes, J W 1994 Fine root dynamics in a northern hardwood forest ecosystem, Hubbard Brook Experimental Forest, NH. J. Ecol. 82, 533–548.Google Scholar
  55. Farrish, K W 1991 Spatial and temporal fine-root distribution in three Louisiana forest soils. Soil Sci. Soc. Am. J. 55, 1752–1757.Google Scholar
  56. Field, C B 1991 Ecological scaling of carbon gain to stress and resource availability. In Response of Plants to Multiple Stresses. Eds. H AMooney, W EWinner and E JPell. pp 35–61. Academic Press, London, UK.Google Scholar
  57. Fogel, R and Hunt, G 1979 Fungal and arboreal biomass in a western Oregon Douglas-fir ecosystem: distribution patterns and turnover. Can. J. For. Res. 9, 245–256.Google Scholar
  58. Fogel, R and Hunt, G 1983 Contribution of mycorrhizae and soil fungi to nutrient cycling in a Douglas-fir ecosystem. Can. J. For. Res. 13, 219–232.Google Scholar
  59. Fölster, H, DeLas Salas, G and Khanna, P 1976 A tropical evergreen forest site with perched water table, Magdalena Valley, Columbia. Biomass and bioelement inventory of primary and secondary vegetation. Oecol. Plant. 11, 297–320.Google Scholar
  60. Gholz, H L, Hendry, L C and Cropper, W PJr 1986 Organic matter dynamics of fine roots in plantations of slash pine (Pinus elliotti) in north Florida. Can. J. For. Res. 16, 529–538.Google Scholar
  61. Goaster, S Le, Dambrine, E and Ranger, J 1991 Croissance et nutrition minérale d'un peuplement d'épicéa sur sol pauvre. I. Évolution de la boimasse et dynamique d'incorporation d'éléments minéraux. Acta Oecol. 12, 771–789.Google Scholar
  62. Gomez, M M and Day, F PJr 1982 Litter nutrient content and production in the Great Dismal Swamp. Am. J. Bot. 69, 1314–1321.Google Scholar
  63. Gower, S T 1987 Relations between mineral nutrient availability and fine root biomass in two Costa Rican tropical wet forests. Biotropica 19, 171–175.Google Scholar
  64. Gower, S T, Isebrands, J G and Sheriff, D W 1995 Carbon allocation and accumulation in conifers. In Resource Physiology of Conifers: Acquisition Allocation, and Utilization. Eds. W K Smith and T MHinckley. Academic Press, New York, USA.Google Scholar
  65. Gower, S T, Vogt, K A and Grier, C C 1992 Carbon dynamics of Rocky Mountain Douglas-fir: influence of water and nutrient availability. Ecol. Monogr. 62, 43–65.Google Scholar
  66. Gower S T, Running S W, Gholz H L, Haynes B E, Hunt J E R, Ryan M G, Waring R H and Cropper J W P 1996 Influence of climate and nutrition on carbon allocation and net primary production of four conifer forests. Tree Physiol. (In press).Google Scholar
  67. Greenland, D J and Kowal, J M 1960 Nutrient content of moist tropical forest in Ghana. Plant and Soil 12, 154–174.Google Scholar
  68. Grier, C C 1976 Biomass productivity and nitrogen-phosphorus cycles in hemlock-spruce stands of the central Oregon coast. In Western Hemlock Management. Eds. W AAtkinson and R JZasoski. pp 71–81. University of Washington Press, Seattle, Washington, USA.Google Scholar
  69. Grier, C C and Running, S W 1976 Leaf area of mature northwestern coniferous forests: relation to site water balance. Ecology 58, 893–899.Google Scholar
  70. Grier, C C and Logan, R S 1977 Old growth Pseudotsuga menziesii communities of a western Oregon watershed: Biomass distribution and production budgets. Ecol. Monogr. 47, 373–400.Google Scholar
  71. Grier, C C and Ballard, T M 1981 Biomass, nutrient distribution, and net production in alpine communities of the Kluane Mountains, Yukon Territory, Canada. Can. J. Bot. 59, 2635–2649.Google Scholar
  72. Grier, C C, Vogt, K A, Keyes, M R and Edmonds, R L 1981 Biomass distribution and above- and belowground production in young and mature Abies amabilis zone ecosystems of the Washington Cascades. Can. J. For. Res. 11, 155–167.Google Scholar
  73. Grubb, P J and Tanner, E V J 1976 The montane forests and soils of Jamaica: a reassessment. J. Arnold Arboretum 57, 513–568.Google Scholar
  74. Harris, W F, Sollins, P, Edwards, N T, Dinger, B E and Shugart, H H 1975 Analysis of carbon flow and productivity in a temperate deciduous forest ecosystem. In Productivity of World Ecosystems. Eds. D EReichle, J FFranklin and D WGoodall. pp 116–122. National Academy of Science, Washington D.C., USA.Google Scholar
  75. Hase, H and Fölster, H 1982 Bioelement inventory of a tropical (semi-) evergreen seasonal forest on eutropic alluvial soils, Western Llanos, Venezuela. Acta Oecol./Oecol. Plant. 3, 331–346.Google Scholar
  76. Haynes, B E and Gower, S T 1995 Belowground carbon allocation in unfertilized and fertilized red pine plantations in northern Wisconsin. Tree Physiol. 15, 317–325.PubMedGoogle Scholar
  77. Helmisaari, H-S 1995 Nutrient cycling in Pinus sylvestris stands in eastern Finland. Plant and Soil 168/169, 327–336.Google Scholar
  78. Hendrick, R L and Pregitzer, K S 1993 The dynamics of fine root length, biomass, and nitrogen content in two northern hardwood ecosystems. Can. J. For. Res. 23, 2507–2520.Google Scholar
  79. Horner, J D, Cates, R G and Gosz, J R 1987 Tannin, nitrogen, and cell wall composition of green vs. senescent Douglas-fir foliage. Within- and between-stand differences in stands of unequal density. Oecologia 72, 515–519.Google Scholar
  80. Huntington, T G, Ryan, D F and Hamburg, S P 1988 Estimating soil nitrogen and carbon pools in a northern hardwood forest ecosystem. Soil Sci. Soc. Am. J. 52, 1162–1167. 1989Google Scholar
  81. Husni, Mohd. Shariff A and Miller, H G 1991 Soil fertility and tree species diversity in two Malaysian forests. J. Trop. For. Sci. 3, 318–331.Google Scholar
  82. Huttel, Ch 1969 Rapport d'Activité l'Année 1968. Off. Rech. Sci. 084 Technique Outremer, Centre d'Adiopodoume, Cote d'Ivoire.Google Scholar
  83. Huttell, C 1975 Root distribution and biomass in three Ivory Coast rain forest plots. In Tropical Ecological Systems. Trends in Terrestrial and Aquatic Research. Eds. F BGolley and EMedina. pp 123–130. Springer-Verlag, New York, USA.Google Scholar
  84. Huttel, C and Bernhard-Reversat, F 1975 Recherches sur l'écosystéme de al forét sub-êquatoriale de Basse Côte-d'Ivoire. Terre Vie Rev. Écol. Appl. 29, 169–264.Google Scholar
  85. Ingestad, T and Agren, G 1992 Theories and methods on plant nutrition and growth. Physiol. Plant. 84, 177–184.CrossRefGoogle Scholar
  86. Jenkinson, D S, Adams, D E and Wild, A 1991 Model estimates of CO2 emissions from soil in response: to global warming. Nature 351, 304–306.CrossRefGoogle Scholar
  87. Jianping, S, Dali, T, Sidong, Z and Miao, W 1993 Fine root dynamics of broadleaved Korean pine forest in Changbai Mountain, China. Chinese J. Appl. Ecol. 4, 241–245.Google Scholar
  88. Johnson, D W, Cole, D W, Bledsoe, C S, Cromack, KJr, Edmonds, R L, Gessel, S P, Grier, C C, Richards, B N and Vogt, K A 1982 Nutrient cycling in forests of the Pacific Northwest. In Analysis of Coniferous Forest Ecosystems in the Western United States. US/IBP Synthesis Series 14. Ed. R LEdmonds. pp 186–232. Hutchinson Ross Publishing Co., Pennsylvania, USA.Google Scholar
  89. Jordan, C F 1971 Productivity of a tropical forest and its relation to a world pattern of energy storage. J. Ecol. 59, 127–142.Google Scholar
  90. Joslin, J D and Anderson, G S 1987 Organic matter and nutrients associated with fine root turnover in a white oak stand. For. Sci. 33, 330–346.Google Scholar
  91. Kangas, P 1992 Root regrowth in a subtropical wet forest in Puerto Rico. Biotropica 24, 463–465.Google Scholar
  92. Kaul, O N, Single, R P, Srivastava, V K and Gurumurti, K 1982 Distribution of organic matter in Pinus elliottii plantations. Indian For. 108, 39–50.Google Scholar
  93. Keyes, M R and Grier, C C 1981 Below- and above-ground biomass and net production in two contrasting Douglas-fir stands. Can. J. For. Res. 11, 599–605.Google Scholar
  94. Kimmins, J P and Hawkes, B C 1978 Distribution and chemistry of fine roots in a white spruce- subalpine fir stand in British Columbia: Implications for management. Can. J. For. Res. 8, 265–279.Google Scholar
  95. Kinerson, R S, Ralston, C W and Wells, C G 1977 Carbon cycling in a loblolly pine plantation. Oecologia 29, 1–10.Google Scholar
  96. Klinge, H 1973 Root mass estimation in lowland tropical rain forests of central Amazonia, Brazil. I. Fine root masses of a pale yellow latosol and a giant humus podzol. Trop. Ecol. 14, 29–38.Google Scholar
  97. Klinge, H 1975 Root mass estimation in lowland tropical rainforests of central Amazonia, Brazil. III. Nutrients in fine roots from giant humus podsols. Trop. Ecol. 16, 28–38.Google Scholar
  98. Klinge, H and Rodrigues, W A 1968a Litter production in an area of Amazonian terra firme forest. Part I. Litter-fall, organic carbon and total nitrogen contents of litter. Amazonian 1, 287–302.Google Scholar
  99. Klinge, H and Rodrigues, W A 1968b Litter production in an area of Amazonian terra firme forest. Part II. Mineral nutrient content of the litter. Amazonian 1, 303–310.Google Scholar
  100. Klinge, H and Herrera, R 1978 Biomass studies in Amazon caatinga forest in southern Venezuela. I. Standing crop of composite root mass in selected stands. Trop. Ecol. 19, 93–110.Google Scholar
  101. Klinge, H, Rodrigues, W A, Brunig, E and Fittkau, E J 1975 Biomass and structure in a central Amazonian rainforest. In Tropical Ecological Systems. Trends in Terrestrial and Aquatic Research. Eds. F BGolley and EMedina. pp 115–122. Springer-Verlag, Berlin, Germany.Google Scholar
  102. Kummerow, J, Castillanos, J, Maas, M and Larigauderie, A 1990 Production of fine roots and the seasonality of their growth in a Mexican deciduous dry forest. Vegetation 90, 73–80.Google Scholar
  103. Lambers, H and Poorter, H 1992 Inherent variation in growth rate between higher plants: a search for physiological causes and ecological consequences. Adv. Ecol. Res. 23, 187–261.Google Scholar
  104. Landsberg J J, Linder S and McMurtrie R E 1995 A strategic plan for research on managed forest ecosystems in a globally changing environment. Global Change and Terrestrial Ecosystems GCTE Report No. 4. GCTE Activity 3.5: Effects of Global Change on Managed Forests. Implementation Plan, pp 1–17.Google Scholar
  105. Landsberg, J J, Kaufmann, M R, Binkley, D, Isebrands, J and Jarvis, P G 1991 Evaluating progress towards closed forest models based on fluxes of carbon, water and nutrients. Tree Physiol. 9, 1–15.PubMedGoogle Scholar
  106. Lawson, G W, Armstrong-Mensah, K O and Hall, J B 1970 A catena in tropical moist deciduous forest near Kade, Ghana. J. Ecol. 58, 371–398.Google Scholar
  107. Linder, S and Axelsson, B 1982 changes in carbon uptake and allocation patterns as a result of irrigation and fertilization in a young Pinus sylvestris stand. In Carbon Uptake and Allocation: Key to Management of Subalpine Forest Ecosystems. Ed. R HWaring. pp 38–44. IUFRO Workshop. For. Res. Lab., Oregon State University Corvallis Oregon USA.Google Scholar
  108. Lodge, D J, Scatena, F N, Asbury, C E and Sanchez, M J 1991 Fine litterfall and related nutrient inputs resulting from Hurricane Hugo in subtropical wet and lower montane rain forests of Puerto Rico. Biotropica 23, 336–342.Google Scholar
  109. Lugo, A E 1992 Comparison of tropical tree plantations with secondary forest, of similar age. Ecol. Monogr. 62, 1–41.Google Scholar
  110. Lugo, A E and Scatena, F N 1995 Ecosystem-level properties of the Luquillo Experimental forest with emphasis on the Forest. In Tropical Forests: Management and Ecology. Ecological Studies. 112. Eds. A ELugo and CLowe. pp. 59–100. Springer-Verlag, New York, USA.Google Scholar
  111. Luxmoore, R J, Oren, R, Sheriff, D W and Thomas, R B 1995 Sourcesink-storage relationships of conifers. In Resource Physiology of Conifers: Acquisition, Allocation, and Utilization. Eds. W KSmith and T MHinckley. pp 179–216. Academic Press, New York, USA.Google Scholar
  112. Mabberley, D J 1992 Tropical Rain Forest Ecology. 2nd Ed. Chapman and Hall, New York, USA. 300 p.Google Scholar
  113. Malkönen, E 1975 Annual primary production and nutrient cycle in a birch stand. Commun. Inst. For. Fenn. 91, 1–35.Google Scholar
  114. Marshall, J D and Waring, R H 1985 Predicting fine root production and turnover by monitoring root starch and soil temperature. Can. J. For. Res. 15, 791–800.Google Scholar
  115. McClaugherty, C A, Aber, J D and Melillo, J M 1982 The role of fine roots in the organic matter and nitrogen budgets of two forested ecosystems. Ecology 63, 1481–1490.Google Scholar
  116. McClaugherty, C A, Aber, J D and Melillo, J M 1984 Decomposition dynamics of fine roots in forested ecosystems. Oikos 42, 378–386.Google Scholar
  117. McGinty D T 1976 Comparative root and soil dynamics on a white pine watershed and in the hardwood forest in the Coweeta Basin. Unpublished Ph.D. Dissertation. University of Georgia, Athens, Georgia, USA.Google Scholar
  118. Megonigal, J P and Day, F PJr 1988 Organic matter dynamics in four seasonally flooded forest communities of the Dismal Swamp. Am. J. Bot. 75, 1334–1343.Google Scholar
  119. Meier C 1981 The role of fine roots in N and P budgets in young and mature Abies amabilis ecosystems. Ph.D. Dissertation. University of Washington, Seattle, WA, USA.Google Scholar
  120. Merckx, R, denHartog, A and VanVeen, J A 1985 Turnover of rootderived material and related microbial biomass formation in soils of different texture. Soil Biol. Biochem. 17, 565–569.CrossRefGoogle Scholar
  121. Mooney, H A and Dunn, E L 1970 Photosynthetic systems of Mediterranean climate shrubs and trees of California and Chile. Am. Nat. 104, 447–453.CrossRefGoogle Scholar
  122. Mooney, H A, Drake, B G, Luxmoore, R J, Oechel, W C and Pitelka, L F 1991 Predicting ecosystem responses to elevated CO2 concentrations. Bio Sci. 41, 96–104.Google Scholar
  123. Nadelhoffer, K J, Aber, J D and Melillo, J M 1983 Leaf litter production and soil organic matter dynamics along a nitrogen availability gradient in southern Wisconsin (USA). Can. J. For. Res. 13, 12–21.Google Scholar
  124. Nadelhoffer, K J, Aber, J D and Melillo, J M 1985 Fine roots, net primary production and nitrogen availability: a new hypothesis. Ecology 66, 1377–1390.Google Scholar
  125. Nilsson, U and Albrektson, A 1993 Productivity of needles and allocation of growth in young Scots pine trees of different competitive status. For. Ecol. Manage. 62, 173–187.Google Scholar
  126. Nye, P H 1961 Organic matter and nutrient cycles under moist tropical forest. Plant and Soil 13, 333–346.Google Scholar
  127. Odum, H T 1970 Summary: an emerging view of the ecological system at El Verde. In A Tropical Rain Forest. Eds. H TOdum and R FFigeon. Ch. 1–10. US Atomic Energy Commission, Div. Tech. Inf Nat. Tech. Inf Serv., Springfield, Virginia, USA.Google Scholar
  128. Ogawa, H, Yoda, K, Ogino, K and Kira, T 1965 Comparative ecological studies of three main types of forest vegetation in Thailand. 2. Plant biomass. Nature Life Southeast Asia 4, 49–81.Google Scholar
  129. O'Neill, R V and DeAngelis, D L 1982 Comparative productivity and biomass relations of forest ecosystems. In Dynamic Properties of Forest Ecosystems. International Biological Programme 23. Ed. D EReichle. pp 411–449. Cambridge University Press, London, UK.Google Scholar
  130. Ovington, J D and Olson, J S 1970 Biomass and chemical content of El Verde Lower Montane rain forest plants. In A Tropical Rain Forest. Eds. H TOdum and R FPigeon. Ch. 11–2. USA tomic Energy Commission, Div. Tech. Inf Nat. Tech. Inf Serv., Springfield, Virginia, USA.Google Scholar
  131. Owen, T H 1954 Observations on the monthly litterfall and nutrient content of Sitka spruce litter. Forestry 27, 7–15.Google Scholar
  132. Pallardy, S G, Cermak, J, Ewers, F W, Kaufmann, M R, Parker, W C and Sperry, J S 1995. Water transport dynamics in trees and stands. In Resource Physiology of Conifers: Acquisition, Allocation, and Utilization. Eds. W KSmith and T MHinckley. pp 301–389. Academic Press, New York, USA.Google Scholar
  133. Pastor, J P, Aber, J D, McClaugherty, C A and Melillo, J M 1984 Aboveground production and N and P cycling along a nitrogen mineralization gradient on Blackhawk Island, Wisconsin. Ecology 65, 256–268.Google Scholar
  134. Persson, H 1978 Root dynamics in a young Scots pine stand in central Sweden. Oikos 30, 508–519.Google Scholar
  135. Persson, H 1980 Death and replacement of fine roots in a mature Scots pine stand. Ecol. Bull. (Stockholm) 32, 251–260.Google Scholar
  136. Post, W M, Emanuel, W R, Zinke, P J and Stangenberger, A G 1982 Soil carbon pools and world life zones. Nature 298, 156–159.Google Scholar
  137. Powell, S W and Day, F PJr 1991 Root production in four communities in the Great Dismal Swamp. Am. J. Bot. 78, 288–297.Google Scholar
  138. Priess, J and Fölster, H 1994 Carbon cycle dynamics and soil respiration of forests under natural degradation in the Gran Sabana. Intersciencia 19, 317–322.Google Scholar
  139. Puri, S, Singh, V, Bhushan, B and Singh, S 1994 Biomass production and distribution of roots in three stands of Populus deltoides. For. Ecol. Manage. 65, 135–147.Google Scholar
  140. Raich, J W and Nadelhoffer, K J 1989 Belowground carbon allocation in forest ecosystems: global trends. Ecology 70, 1346–1354.Google Scholar
  141. Rastetter, E B, King, A W, Cosby, B J, Hornberger, G M, O'Neill, R V and Hobbie, J H 1992 Aggregating fine-scale ecological knowledge to model coarser-scale attributes of ecosystems. Ecol. Appl. 2, 44–70.Google Scholar
  142. Reich, P B, Walters, M B and Ellsworth, D S 1992 Leaf life-span in relation to leaf, plant, and stand characteristics among diverse ecosystems. Ecol. Monogr. 62, 365–392.Google Scholar
  143. Roy, S and Singh, J S 1995 Consequences of habitat heterogeneity for availability of nutrients in a dry tropical forest. J. Ecol. 82, 503–509.Google Scholar
  144. Ruark, G A and Bockheim, J G 1987 Below-ground biomass of 10-, 20-, and 32-year-old Populus tremuloides in Wisconsin. Pedobiologia 30, 207–217.Google Scholar
  145. Running, S W and Hunt, J E R 1993 Generalization of a forest ecosystem process model for other biomes, BIOME-BGC, and an application for global-scale models. In Scaling Physiological Processes: Leaf to Globe. Eds. J REhleringer and C BField. pp 141–156. Academic Press, New York, USA.Google Scholar
  146. Safford, L O 1974 Effect of fertilization on biomass and nutrient content of fine roots in a beech-birch-maple stand. Plant and Soil 40, 349–363.Google Scholar
  147. Sanford, R LJr 1989 Root systems of three adjacent, old growth Amazon forests and associated transition zones. J. Trop. For. Sci. 1, 268–279.Google Scholar
  148. Sanford, R LJr 1989 Apogeotropic roots in an Amazon rain forest. Science 235, 1062–1064.Google Scholar
  149. Santantonio, D 1990 Modeling growth and production of tree roots. In Process Modeling of Forest Growth Responses to Environmental Stress. Eds. R KDixon, R SMeldahl, G ARuark and W GWarren. pp 124–141. Timber Press, Portland, Oregon, USA.Google Scholar
  150. Santantonio, D and Herrmann, R K 1985 Standing crop, production, and turnover of fine roots on dry, moderate, and wet sites of mature Douglas-fir in western Oregon. Ann. Sci. For. 42, 113–142.Google Scholar
  151. Santantonio, D and Santantonio, E 1987 Effect of thinning on production and mortality of fine roots in a Pinus radiata plantation on a fertile site in New Zealand. Can. J. For. Res. 17 919–928.Google Scholar
  152. Santantonio, D and Grace, J C 1987 Estimating fine-root production and turnover from biomass and decomposition data: a compartment flow model. Can. J. For. Res. 17, 900–908.Google Scholar
  153. Schlesinger, W H 1977 Carbon balance in terrestrial detritus. Annu. Rev. Ecol Syst. 8, 51–81.CrossRefGoogle Scholar
  154. Schulze, E-D 1982 Plant life forms and their carbon, water and nutrient relations. In Physiological Plant Ecology 11. Water Relations and Carbon Assimilation. Eds. O LLange, P SNobel, C BOsmond and HZiegler. pp 616–676. Springer-Verlag, Berlin, Germany.Google Scholar
  155. Singh, J S and Singh, S P 1987 Forest vegetation of the Himalaya. The Bot. Rev. 53, 80–192.Google Scholar
  156. Singh, V 1994 Root distribution in Pinus deltoides “G-3” plantations in an arid region of northwestern India. Trop. Ecol. 35, 105–113.Google Scholar
  157. Sollins, P, Grier, C C, McCorison, F M, Cromack, KJr, Fogel, R and Frederikson, R L 1980 The internal element cycles of an old growth Douglas-fir ecosystem in western Oregon. Ecol. Monogr. 50, 261–285.Google Scholar
  158. Son, Y and Gower, S T 1991 Aboveground nitrogen and phosphorus use by five plantation-grown trees with different leaf longevities. Biogeochemistry 14, 167–191.Google Scholar
  159. Sprugel, D G, Ryan, M K, Brooks, J R, Vogt, K A and Martin, T A 1994 Respiration, from the organ-level to the stand-a model system for the application of scaling techniques. In Resource Physiology of Conifers. Acquisition, Allocation, and Utilization. Eds. W KSmith and T MHinckley. pp 255–299. Academic Press. San Diego, New York, USA.Google Scholar
  160. Spycher, G, Sollins, P and Rose, S 1983 Carbon and nitrogen in the light fraction of a forest soil: vertical distribution and seasonal patterns. Soil Sci. 135, 79–87.Google Scholar
  161. Srivastava, S K, Singh, K P and Upadhyay, R S 1986 Fine root growth dynamics in teak (Tectona grandis Linn.F.). Can. J. For. Res. 16, 1360–1364.Google Scholar
  162. Stark, N and Spratt, M 1977 Root biomass and nutrient storage in rain forest oxisols near San Carlos de Rio Negro. Trop. Ecol. 18, 1–9.Google Scholar
  163. Swank, W T and Crossley, D A 1988 Introduction and site description. In Forest Hydrology and Ecology at Coweeta. Eds. W TSwank and D ACrossleyJr. pp 3–16. Springer-Verlag, New York, USA.Google Scholar
  164. Swift, M J, Heal, O W and Anderson, J M 1979 Decomposition in Terrestrial Ecosystems. Blackwell Publications, Oxford, UK.Google Scholar
  165. Tanner, E V J 1977 Four montane rain forests of Jamaica: a quantitative characterization of the floristics, the soils and the foliar mineral levels, and a discussion of the interrelations. J. Ecol. 65, 883–918.Google Scholar
  166. Tanner, E V J 1980a Studies on the biomass and productivity in a series of montane rain forests in Jamaica. J. Ecol. 68, 573–588.Google Scholar
  167. Tanner, E V J 1980b Litterfall in montane rain forests of Jamaica and its relation to climate. J. Ecol. 68, 833–848.Google Scholar
  168. Tanner, E V J 1985 Jamaican montane forests: nutrient capital and cost of growth. J. Ecol. 73, 553–568.Google Scholar
  169. Teskey, R O and Hinckley, T M 1981 Influence of temperature and water potentials on root growth of white oak. Physiol. Plant. 52, 363–369.Google Scholar
  170. Turner J 1975 Nutrient cycling in a Douglas-fir ecosystem with respect to age and nutrient status. Unpublished Ph.D. Dissertation, University of Washington, Seattle, Washington, USA.Google Scholar
  171. Valentini, R, Mugnozza, G E S and Ehleringer, J R 1992 Hydrogen and carbon isotope ratios of selected species of a Mediterranean macchia ecosystem. Funct. Ecol. 6, 627–631.Google Scholar
  172. Vance, E D and Nadkarni, N M 1992 Root biomass distribution in a moist tropical montane forest. Plant and Soil 142, 31–39.Google Scholar
  173. VanPraag, H J, Sougnez-Remy, S, Weissen, F and Carletti, G 1988 Root turnover in a beech and a spruce stand of the Belgian Ardennes. Plant and Soil 105, 87–103.Google Scholar
  174. Viereck, L A, Dyrness, C T, VanCleve, K and Foote, M J 1983 Vegetation, soils, and forest productivity in selected forest types in interior Alaska. Can. J. For. Res. 13, 703–720.Google Scholar
  175. Visalakshi, N 1994 Fine root dynamics in two tropical dry evergreen forests in southern India. J. Biosci. 19, 103–116.Google Scholar
  176. Vitousek, P 1982 Nutrient cycling and nutrient use efficiency. Am. Nat. 119, 553–572.CrossRefGoogle Scholar
  177. Vitousek, P M, Gosz, J R, Grier, C C, Melillo, J M and Reiners, W A 1982 A comparative analysis of potential nitrification and nitrate mobility in forest ecosystems. Ecol. Monogr. 52, 155–177.Google Scholar
  178. Vitousek, P M and Sanford, R LJr 1986 Nutrient cycling in moist tropical forests. Annu. Rev. Ecol. Syst. 17, 137–167.CrossRefGoogle Scholar
  179. Vogt D J 1987 Douglas-fir ecosystems in western Washington biomass and production as related to site quality and stand age. Ph.D. Dissertation. University of Washington, Seattle, Washington, USA.Google Scholar
  180. Vogt, K A 1991 Carbon cycling in forest ecosystems. Tree Physiol. 9, 69–86.PubMedGoogle Scholar
  181. Vogt, K A, Grier, C C, Meier, C E and Edmonds, R L 1982 Mycorrhizal role in net primary production and nutrient cycling in Abies amabilis ecosystems in western Washington. Ecology 63, 370–380.Google Scholar
  182. Vogt, K A, Vogt, D J, Moore, E E, Littke, W, Grier, C and Leney, C 1985 Estimating Douglas-fir fine root biomass and production from living bark and starch. Can. J. For. Res. 15, 177–179.Google Scholar
  183. Vogt, K A Grier, C C and Vogt, D J 1986 Production, turnover, and nutrient dynamics of above and belowground detritus of world forests. Adv. Ecol. Res. 15, 303–377.Google Scholar
  184. Vogt, K A, Dahlgren, R A, Ugolini, F, Zabowski, D, Moore, E E and Zasoski, R J 1987 Above- and belowground: I. Concentrations of Al, Fe, Ca, Mg, K, Mn, Cu, Zn and P for Abies amabilis and Tsuga mertensiana. Biogeochemistry 4, 277–294.Google Scholar
  185. Vogt, K A, Vogt, D J, Moore, E E and Sprugel, D G 1989 Methodological considerations in measuring biomass, production, respiration and nutrient resorption for tree roots in natural ecosystem. In Applications of Continuous and Steady-State Methods to Root Biology. Eds. J GTorrey and L JWinship. pp 217–232. Kluwer Academic Publishers, Dordrecht, the Netherlands.Google Scholar
  186. Vogt, K A, Vogt, D J, Gower, S T and Grier, C C 1990 Carbon and nitrogen interactions for forest ecosystems. In Above- and belowground interactions in forest trees in acidified soils. Air Pollution Report 32. Ed. H Persson. pp 203–235. Commission of the European Communities. Directorate-General for Science, Research and Development. Environment Research Programme, Brussels, Belgium.Google Scholar
  187. Vogt, K A, Publicover, D A, Bloomfield, J, Perez, J M, Vogt, D J and Silver, W L 1993 Belowground responses as indicators of environmental change. Environ. Exp. Bot. 33, 189–205.CrossRefGoogle Scholar
  188. Vogt, K A, Vogt, D, Brown, S, Tilley, J Edmonds, R, Silver, W and 0911 0406 V 2 Siccama, T 1995 Forest floor and soil organic matter contents and factors controlling their accumulation in boreal temperate and tropical forests. Adv. Soil Sci. 159–178.Google Scholar
  189. Vogt, K A, Gordon, J C, Wargo, J P, Vogt, D J, Asbjornsen, H, Palmiotto, P A, Clark, H J, O'Hara, J L, Keeton, W S and Patel-Weynand, T 1996 Ecosystems: Balancing Science with Management. Springer-Verlag, New York, USA.Google Scholar
  190. Waring, R H and Franklin, J F 1979 The evergreen coniferous forests of the Pacific Northwest. Science 204, 1380–1386.Google Scholar
  191. Waring, R H 1987 Characteristics of trees predisposed to die: stress causes distinctive changes in photosynthate allocation. BioSci. 37, 569–574.Google Scholar
  192. Waring, R H and Schlesinger, W H 1985 Forest Ecosystems: Concepts and Management. Academic Press, Orlando, Florida, USA.Google Scholar
  193. Welch, T G and Klemmedson, J O 1975 Influence of the biotic factor and parent material on distribution of nitrogen and carbon on ponderosa pine ecosystems. In Forest Soils and Forest Land Management. Eds. BBernier and C HWinget. pp 159–178. University of Laval Press, Quebec, Canada.Google Scholar
  194. White, C S, Gosz, J R, Horner, J D and Moore, D I 1988 Seasonal, annual, and treatment-induced variation in available nitrogen pools and nitrogen-cycling processes in soils of two Douglas-fir stands. Biol. Fertil. Soils 6, 93–99.CrossRefGoogle Scholar
  195. Yin, X, Perry, J A and Dixon, R K 1989 Fine-root dynamics and biomass distribution in a Quercus ecosystem following harvesting. For. Ecol. Manage. 27, 159–177.Google Scholar
  196. Yoda, K and Kira, T 1969 Comparative ecological studies on three main types of forest vegetation in Thailand. 5. Accumulation and turnover of soil organic matter, with notes on the altitudinal soil secyuence on Khao (Mt.) Luang, peninsular Thailand. nature Life Southeast Asia 6, 88–110.Google Scholar

Copyright information

© Kluwer Academic Publishers 1996

Authors and Affiliations

  • Kristiina A. Vogt
    • 1
  • Daniel J. Vogt
    • 1
  • Peter A. Palmiotto
    • 1
  • Paul Boon
    • 1
  • Jennifer O'Hara
    • 1
  • Heidi Asbjornsen
    • 1
  1. 1.School of Forestry and Environmental StudiesNew HavenUSA

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