Leaf and root production, decomposition and carbon and nitrogen fluxes during stand development in tropical moist forests, north-east India
C. Lalnunzira A and S. K. Tripathi A B
+ Author Affiliations
- Author Affiliations
A Department of Forestry, School of Earth Sciences and Natural Resources Management, Mizoram University, Aizawl, Tanhril -796004, India.
B Corresponding author. Email: sk_tripathi@rediffmail.com
Soil Research 56(3) 306-317 https://doi.org/10.1071/SR16265
Submitted: 3 October 2016 Accepted: 10 November 2017 Published: 16 March 2018
Abstract
In the present study we investigated the production and decomposition of leaves, branches and roots in two moist regenerating tropical forests (5 and 15 years old; RF-5 and RF-15 respectively) and a natural forest (NF) in north-east India. Total litter input increased during vegetation succession (759, 1089 and 1284 g m–2 year–1 in RF-5, RF-15 and NF respectively), whereas the contribution of soft litter decreased sharply. Decomposition over 450 days indicated significant seasonal (P < 0.001) patterns in mass loss of litter components, with greater rates during the wet period. Soil CO2 efflux was strongly seasonal. C stock loss followed patterns similar to those of mass loss, whereas N increased initially, followed by its gradual release. Rainfall explained 74–90% of the variability in mass loss rates. Concentrations of cellulose and N were significantly positively correlated with mass loss at an early stage of decomposition (r = 0.54–0.65, P < 0.05), whereas lignin : N and C : N ratios were negatively correlated with mass loss at later stages. Regenerating forests adapted ecosystem-level strategies that induced early leaf fall to reduce soil water loss, increase organic matter return to the soil and conserve N through immobilisation during the process of decomposition to speed up vegetation succession in the regenerating forest.
Additional keywords: carbon and nitrogen dynamics, litter production, natural tropical forest, regenerating forests.
References
Aide TM, Grau HR (2004) Globalization, migration, and Latin American ecosystems. Science 305, 1915–1916.| Globalization, migration, and Latin American ecosystems.Crossref | GoogleScholarGoogle Scholar |
Anderson JM, Ingram ISI (1993) ‘Tropical soil biology and fertility: a handbook of methods.’ 2nd edn. (CAB International: Wallingford, UK)
Austin AT, Vitousek PM (2000) Precipitation, decomposition and litter decomposability of Metrosideros polymorpha in native forests on Hawai. Journal of Ecology 88, 129–138.
| Precipitation, decomposition and litter decomposability of Metrosideros polymorpha in native forests on Hawai.Crossref | GoogleScholarGoogle Scholar |
Bocock KL, Gilbert D, Capstick CK, Twin DC, Ward JS, Woodman MJ (1960) Changes in leaf litter when placed on the surface of the soils with contrasting humus types I. Losses in dry weight of oak and ash leaf litter. Journal of Soil Science 11, 1–9.
| Changes in leaf litter when placed on the surface of the soils with contrasting humus types I. Losses in dry weight of oak and ash leaf litter.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF3MXht1Kqtr8%3D&md5=5e0c6fe769aeb2935b8b788dd5629c03CAS |
Boyero L, Cardinale BJ, Bastian M, Pearson RG (2014) Biotic vs. abiotic control of decomposition: a comparison of the effects of simulated extinctions and changes in temperature. PLoS One 9, e87426
| Biotic vs. abiotic control of decomposition: a comparison of the effects of simulated extinctions and changes in temperature.Crossref | GoogleScholarGoogle Scholar |
Celentano D, Zahawi RA, Finegan B, Ostertag R, Cole RJ, Holl KD (2011) Litterfall dynamics under different tropical forest restoration strategies in Costa Rica. Biotropica 43, 279–287.
| Litterfall dynamics under different tropical forest restoration strategies in Costa Rica.Crossref | GoogleScholarGoogle Scholar |
Champion HG, Seth SK (1968) ‘A revised survey of the forest types of India.’(Government of India: New Delhi, India)
Chazdon RL (2014) ‘Second growth: the promise of tropical forest regeneration in an age of deforestation.’(University of Chicago Press: Chicago, IL, USA)
Chazdon RL, Letcher SG, van Breugel M, Martinez-Ramos M, Bongers F, Finegan B (2008) Rates of change in tree communities of secondary neotropical forests following major disturbances. Philosophical Transactions of the Royal Society of London B Biological Sciences 362, 273–289.
Chen H, Gurmesa GA, Liu L, Zhang T, Fu S (2014) Effects of litter manipulation on litter decomposition in a successional gradients of tropical forests in southern China. PLoS One 9, e99018
| Effects of litter manipulation on litter decomposition in a successional gradients of tropical forests in southern China.Crossref | GoogleScholarGoogle Scholar |
Denslow JS, Guzman GS (2000) Variation in stand structure, light and seedling abundance across a tropical moist forest chronosequence, Panama. Journal of Vegetation Science 11, 201–212.
| Variation in stand structure, light and seedling abundance across a tropical moist forest chronosequence, Panama.Crossref | GoogleScholarGoogle Scholar |
Economics and Statistics Department Government of Mizoram (2014) ‘State Statistical handbook of Mizoram.’ (Economics and Statistics Department Government of Mizoram: North East India).
Feldpausch TR, Rondon MA, Fernande ECM, Riha SJ, Wandelli E (2004) Carbon and nutrient accumulation in secondary forests regenerating on pastures in Central Amazonia. Ecological Applications 14, 164–176.
| Carbon and nutrient accumulation in secondary forests regenerating on pastures in Central Amazonia.Crossref | GoogleScholarGoogle Scholar |
Finzi AC, Allen AS, DeLucia EH, Ellsworth DS, Schlesinger WH (2001) Forest litter production, chemistry and decomposition following two years of free-air CO2 enrichment. Ecology 82, 470–484.
Fioretto A, Papa S, Fuggi A (2003) Litterfall and litter decomposition in a low Mediterranean shrubland. Biology and Fertility of Soils 39, 37–44.
| Litterfall and litter decomposition in a low Mediterranean shrubland.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXptVyqsrY%3D&md5=9a967dfb14b3057fce07a2260b0054bdCAS |
Gavazov K, Mills R, Spiegelberger T, Lenglet J, Buttler A (2014) Biotic and abiotic constraints on the decomposition of Fagussylvaticaleaf litter along an altitudinal gradient in contrasting land-use types. Ecosystems 17, 1326–1337.
| Biotic and abiotic constraints on the decomposition of Fagussylvaticaleaf litter along an altitudinal gradient in contrasting land-use types.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXht1Wlsr3J&md5=13d0dd2db18ca3d2b412cb029c6e06b0CAS |
Hauser S, Gang E, Norgrove L, Birang MA (2005) Decomposition of plant material as an indicator of ecosystem disturbance in tropical land use systems. Geoderma 129, 99–108.
| Decomposition of plant material as an indicator of ecosystem disturbance in tropical land use systems.Crossref | GoogleScholarGoogle Scholar |
Hobbie SE, Oleksyn J, Eissenstat DM, Reich PB (2009) Fine root decomposition rates do not mirror those of leaf litter among temperate tree species. Oecologia 162, 505–513.
Holl KD (2002) Tropical moist forest restoration. In ‘Handbook of ecological restoration’, Vol. II. (Eds A. J. Davy and M. Perrow.) pp. 539–558. (Cambridge University Press: Cambridge, UK)
Jordon CF (1983) Productivity of tropical rain forest ecosystems and the implications for their useas future wood and energy sources. In ‘Tropical rainforests ecosystems –structure and function’. (Ed. F. B. Golley) pp. 117–136. (Elsevier Scientific Publishing: Oxford, UK)
Kotowska MM, Leuschner C, Triadiati T, Hertel D (2015) Conversion of tropical lowland forest reduces nutrient return through litterfall, and alters nutrient use efficiency and seasonality of net primary production. Oecologia 180, 601–618.
| Conversion of tropical lowland forest reduces nutrient return through litterfall, and alters nutrient use efficiency and seasonality of net primary production.Crossref | GoogleScholarGoogle Scholar |
Lam PKS, Dudgeon D (1985) Seasonal effects on litterfall in a Hong Kong forest. Journal of Tropical Ecology 1, 55–64.
| Seasonal effects on litterfall in a Hong Kong forest.Crossref | GoogleScholarGoogle Scholar |
Lambers H, Raven JA, Shaver GR, Smith SE (2008) Plant nutrient-acquisition strategies change with soil age. Trends in Ecology & Evolution 23, 95–103.
| Plant nutrient-acquisition strategies change with soil age.Crossref | GoogleScholarGoogle Scholar |
Lewis SL, Edwards DP, Galbraith D (2015) Increasing human dominance of tropical forests. Science 349, 827–832.
| Increasing human dominance of tropical forests.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXhtlKltrbO&md5=18997880bc923379d7fe2e11a247e035CAS |
Loaiza-Usuga JC, León-Peláez JD, González-Hernández MI, Gallardo-Lancho JF, Osorio-Vega W, Correa-Londoño G (2013) Alterations in litter decomposition patterns in tropical montane forests of Colombia: a comparison of oak forests and coniferous plantations. Canadian Journal of Forest Research 43, 1–6.
Marín-Spiotta E, Ostertag R, Silver WL (2007) Long-term patterns in tropical reforestation: plant community composition and aboveground biomass accumulation. Ecological Applications 17, 828–839.
| Long-term patterns in tropical reforestation: plant community composition and aboveground biomass accumulation.Crossref | GoogleScholarGoogle Scholar |
Martin PH, Sherman RE, Fahey TJ (2004) Forty years of tropical forest recovery from agriculture: structure and floristics of secondary and old-growth riparian forests in the Dominican Republic. Biotropica 36, 297–317.
Martius C, Hofer H, Garcia MVB, Rombke J, Hanagarth W (2004) Litter fall, litter stocks and decomposition rates in rainforest and agroforestry sites in central Amazonia. Nutrient Cycle in Agroecosystems 68, 137–154.
Mtambanengwe F, Kirchman H (1995) Litter from tropical savanna woodland (Miombo): chemical composition and C and N mineralization. Soil Biology & Biochemistry 27, 1639–1651.
| Litter from tropical savanna woodland (Miombo): chemical composition and C and N mineralization.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXhtVSntrfJ&md5=0d724f241514a5954961fc1d9a475733CAS |
McClaugherty CA, Aber JD, Melillo JM (1982) The roles of fine roots in organic matter and nitrogen budgets of forest ecosystems. Ecology 63, 1481–1490.
| The roles of fine roots in organic matter and nitrogen budgets of forest ecosystems.Crossref | GoogleScholarGoogle Scholar |
Meentemeyer V, Box EO, Thompson R (1982) World patterns and amounts of terrestrial plant litter production. Bioscience 32, 125–128.
| World patterns and amounts of terrestrial plant litter production.Crossref | GoogleScholarGoogle Scholar |
Odiwe AI, Muoghalu JI (2003) Litterfall dynamics and forest floor litter as influenced by fire in a secondary lowland rain forest in Nigeria. Tropical Ecology 44, 241–248.
Olson JS (1963) Energy storage and the balance of producers and decomposers in ecological systems. Ecology 44, 322–331.
| Energy storage and the balance of producers and decomposers in ecological systems.Crossref | GoogleScholarGoogle Scholar |
Ostertag R, Hobbie SE (1999) Early stages of root and leaf decomposition in Hawaiian forests: effects of nutrient availability. Oecologia 121, 564–573.
| Early stages of root and leaf decomposition in Hawaiian forests: effects of nutrient availability.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC1czns1yktw%3D%3D&md5=9e318138eed13aef1caaa253eec2a6a4CAS |
Ostertag R, Marín-Spiotta E, Silver WL, Schulten J (2008) Litterfall and decomposition in relation to soil carbon pools along a secondary forest chronosequence in Puerto Rico. Ecosystems 11, 701–714.
| Litterfall and decomposition in relation to soil carbon pools along a secondary forest chronosequence in Puerto Rico.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtVOntL7I&md5=724b7ed760f434f5afd521e7d4fcc61bCAS |
Page AL, Miller RL, Keeny DR (Eds) (1982) ‘Methods of soil analysis. Part 2, second edition.’ (American Society of Agnonomy, Soil Science Society of America: Madison, WI, USA)
Pandey RR, Sharma G, Tripathi SK, Singh AK (2007) Litterfall, litter decomposition and nutrient dynamics in a subtropical natural oak forest and managed plantation in northeastern India. Forest Ecology and Management 240, 96–104.
| Litterfall, litter decomposition and nutrient dynamics in a subtropical natural oak forest and managed plantation in northeastern India.Crossref | GoogleScholarGoogle Scholar |
Pandey RR, Sharma G, Singh TB, Tripathi SK (2010) Factors influencing soil CO2 efflux in a north eastern Indian oak forest and plantation. African Journal of Plant Science 4, 280–289.
Pandey S, Sheikh GA, Bhat AH (2016) Dynamics of litterfall in nutrient cycling and forest preservation. International Journal of Multidisciplinary Research 2, 2455–3662.
Paudel E, Dossa GGO, de Blecourt M, Beckschafer P, Xu J, Harrison RD (2015) Quantifying the factors affecting leaf litter decomposition across a tropical forest disturbance gradient. Ecosphere 6, 1–20.
| Quantifying the factors affecting leaf litter decomposition across a tropical forest disturbance gradient.Crossref | GoogleScholarGoogle Scholar |
Pragasan AL, Parthasarathy N (2005) Litter production in tropical dry evergreen forests of south India in relation to season, plant life-forms and physiognomic groups. Current Science 88, 1255–1263.
Purahong W, Schloter M, Pecyna MJ, Kapturska D, Daumlich V, Mital S, Buscot F, Hofrichter M, Gutknecht JLM, Kruger D (2015) Uncoupling of microbial community structure and function in decomposing litter across beech forest ecosystems in central Europe. Scientific Reports 4,
| Uncoupling of microbial community structure and function in decomposing litter across beech forest ecosystems in central Europe.Crossref | GoogleScholarGoogle Scholar |
Roy PS, Roy A (2010) Land use and land cover change in India: a remote sensing and GIS perspective. Journal of the Indian Institute of Science 90, 489–502.
Sayer EJ, Powers JS, Tanner TVJ (2007) Increased litterfall in tropical forest boosts the transfer of soil CO2 to the atmosphere. PLoS One 2, e1299
| Increased litterfall in tropical forest boosts the transfer of soil CO2 to the atmosphere.Crossref | GoogleScholarGoogle Scholar |
Silver WL, Kueppers LM, Lugo AE, Ostertag R, Matzek V (2004) Carbon sequestration and plant community dynamics following reforestation of tropical pasture. Ecological Applications 14, 1115–1127.
| Carbon sequestration and plant community dynamics following reforestation of tropical pasture.Crossref | GoogleScholarGoogle Scholar |
Singh ShB, Mishra BP, Tripathi SK (2015) Recovery of plant diversity and soil nutrients during stand development in subtropical forests of Mizoram, northeast India. Biodiversitas 16, 205–212.
| Recovery of plant diversity and soil nutrients during stand development in subtropical forests of Mizoram, northeast India.Crossref | GoogleScholarGoogle Scholar |
Slik JWF, Paoli G, McGuire K, Amaral I, Barroso J, Bastian M, Blanc L (2013) Large trees drive forest aboveground biomass variation in moist lowland forests across the tropics. Global Ecology and Biogeography 22, 1261–1271.
| Large trees drive forest aboveground biomass variation in moist lowland forests across the tropics.Crossref | GoogleScholarGoogle Scholar |
Stocker GC, Thompson WA, Irvine AK, Fitzsim JD, Thomas PR (1995) Annual patterns of litterfall in a lowland and table- land rainforest in tropical Australia. Biotropica 27, 412–420.
Swamy HR, Proctor J (1994) Litterfall and nutrient cycling in four rainforests in the Sringeri area of the Indian Western Ghats. Global Ecology and Biogeography Letters 4, 155–165.
| Litterfall and nutrient cycling in four rainforests in the Sringeri area of the Indian Western Ghats.Crossref | GoogleScholarGoogle Scholar |
Tripathi SK, Singh KP (1992a) Nutrient immobilization and release pattern during plant decomposition in a dry tropical bamboo savanna, India. Biology and Fertility of Soils 14, 191–199.
| Nutrient immobilization and release pattern during plant decomposition in a dry tropical bamboo savanna, India.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXksVynsbw%3D&md5=f6d833904e57ccf7c20fb5b0c5d95ac8CAS |
Tripathi SK, Singh KP (1992b) Abiotic and litter quality control during the decomposition of different plant parts in dry tropical bamboo savanna in India. Pedobiologia 36, 109–124.
Tripathi SK, Sumida A, Shibata H, Uemura S, Ono K, Hara T (2005) Growth and substrate quality of fine roots and soil nitrogen availability in a young Betula ermanii forest of Northern Japan: effects of the removal of understory dwarf bamboo (Sasa kurilensis). Forest Ecology and Management 212, 278–290.
| Growth and substrate quality of fine roots and soil nitrogen availability in a young Betula ermanii forest of Northern Japan: effects of the removal of understory dwarf bamboo (Sasa kurilensis).Crossref | GoogleScholarGoogle Scholar |
Tripathi SK, Sumida A, Shibata H, Ono K, Uemura S, Kodama Y, Hara T (2006) Leaf litterfall and decomposition of different above- and belowground parts of birch (Betula ermanii) trees and dwarf bamboo (Sasa kurilensis) shrubs in a young secondary forest in Northern Japan. Biology and Fertility of Soils 43, 237–246.
| Leaf litterfall and decomposition of different above- and belowground parts of birch (Betula ermanii) trees and dwarf bamboo (Sasa kurilensis) shrubs in a young secondary forest in Northern Japan.Crossref | GoogleScholarGoogle Scholar |
Uselman SM, Qualls RG, Lilienfein J (2007) Fine root production across a primary successional ecosystem chronosequence at Mt. Shasta, California. Ecosystems 10, 703–717.
| Fine root production across a primary successional ecosystem chronosequence at Mt. Shasta, California.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtFejs7nO&md5=4124b5bcaa35d191b1ba41fe1a64cbe2CAS |
van Breugel M, Bongers F, Marti’Nez-Ramos M (2007) Species dynamics during early secondary forest succession: recruitment, mortality and species turnover. Biotropica 39, 610–619.
| Species dynamics during early secondary forest succession: recruitment, mortality and species turnover.Crossref | GoogleScholarGoogle Scholar |
Vance ED, Brookes PC, Jenkinson DS (1987) An extraction method for measuring soil microbial biomass carbon. Soil Biology & Biochemistry 19, 703–707.
| An extraction method for measuring soil microbial biomass carbon.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXjs1KqsA%3D%3D&md5=5ef618ae2bbf3c60a2c364059b609059CAS |
Vitousek PM (1984) Litterfall, nutrient cycling, and nutrient limitation in tropical forests. Ecology 65, 285–298.
| Litterfall, nutrient cycling, and nutrient limitation in tropical forests.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2cXhtlOqu7c%3D&md5=34576a67720351753d7bd781dd13d535CAS |
Walker J, Reddel P (2007) Retrogressive succession and restoration on old landscapes. In ‘Linking restoration and ecological succession’. (Eds L. R. Walker, J. Walker, and R. J. Hobbs.) pp. 1–16. (Springer Science: New York, NY, USA)
Witkamp M (1966) Rates of carbon dioxide evolution from the forest floor. Ecology 47, 492–494.
| Rates of carbon dioxide evolution from the forest floor.Crossref | GoogleScholarGoogle Scholar |
Xuluc-Tolosa FJ, Vester HFM, Ramírez-Marcial N, Castellanos-Albores J, Lawrence D (2003) Leaf litter decomposition of tree species in three successional phases of tropical dry secondary forest in Campeche, Mexico. Forest Ecology and Management 174, 401–412.
| Leaf litter decomposition of tree species in three successional phases of tropical dry secondary forest in Campeche, Mexico.Crossref | GoogleScholarGoogle Scholar |
Zhang D, Hui D, Luo Y, Zhou G (2008) Rates of litter decomposition in terrestrial ecosystems: global patterns and controlling factors. Journal of Plant Ecology 1, 85–93.
| Rates of litter decomposition in terrestrial ecosystems: global patterns and controlling factors.Crossref | GoogleScholarGoogle Scholar |
Zhang K, Cheng X, Dang H, Ye C, Zhang Y, Zhang Q (2013) Linking litter production, quality and decomposition to vegetation succession following agricultural abandonment. Soil Biology & Biochemistry 57, 803–813.
| Linking litter production, quality and decomposition to vegetation succession following agricultural abandonment.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhslejsrnK&md5=75604103681ebd7bf5d1b3646f3f8fe6CAS |
Zhou GY, Guan LL, Wei XH, Zhang DQ, Zhang QM (2006) Litterfall production along successional and altitudinal gradients of subtropical monsoon evergreen broadleaved forests in Guangdong, China. Plant Ecology 188, 77–89.
| Litterfall production along successional and altitudinal gradients of subtropical monsoon evergreen broadleaved forests in Guangdong, China.Crossref | GoogleScholarGoogle Scholar |
Zhou G, Guan L, Wei X, Tang X, Liu S, Liu J, Zhang D, Yan J (2008) Factors influencing leaf litter decomposition: an intersite decomposition experiment across China. Plant and Soil 311, 61–72.
| Factors influencing leaf litter decomposition: an intersite decomposition experiment across China.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtVyju73J&md5=3ecde636004eee52b7372a9d6e5d9ec3CAS |
