Oecologia

, Volume 174, Issue 4, pp 1449–1461

Temperature and rainfall strongly drive temporal growth variation in Asian tropical forest trees

  • Mart Vlam
  • Patrick J. Baker
  • Sarayudh Bunyavejchewin
  • Pieter A. Zuidema
Global change ecology - Original research

Abstract

Climate change effects on growth rates of tropical trees may lead to alterations in carbon cycling of carbon-rich tropical forests. However, climate sensitivity of broad-leaved lowland tropical trees is poorly understood. Dendrochronology (tree-ring analysis) provides a powerful tool to study the relationship between tropical tree growth and annual climate variability. We aimed to establish climate–growth relationships for five annual-ring forming tree species, using ring-width data from 459 canopy and understory trees from a seasonal tropical forest in western Thailand. Based on 183/459 trees, chronologies with total lengths between 29 and 62 years were produced for four out of five species. Bootstrapped correlation analysis revealed that climate–growth responses were similar among these four species. Growth was significantly negatively correlated with current-year maximum and minimum temperatures, and positively correlated with dry-season precipitation levels. Negative correlations between growth and temperature may be attributed to a positive relationship between temperature and autotrophic respiration rates. The positive relationship between growth and dry-season precipitation levels likely reflects the strong water demand during leaf flush. Mixed-effect models yielded results that were consistent across species: a negative effect of current wet-season maximum temperatures on growth, but also additive positive effects of, for example, prior dry-season maximum temperatures. Our analyses showed that annual growth variability in tropical trees is determined by a combination of both temperature and precipitation variability. With rising temperature, the predominantly negative relationship between temperature and growth may imply decreasing growth rates of tropical trees as a result of global warming.

Keywords

Climate–growth relationship Global change Thailand Tree rings Tropical tree 

Supplementary material

442_2013_2846_MOESM1_ESM.jpg (3.3 mb)
Fig. S1 Ring structure of the five study species, direction of growth is from right to left. White arrows indicate ring boundaries (JPEG 3397 kb)
442_2013_2846_MOESM2_ESM.eps (907 kb)
Fig. S2 Boxplots showing the dbh distribution of all sampled trees and those trees included in the chronology (EPS 906 kb)

References

  1. Baker PJ, Bunyavejchewin S (2006) Suppression, release and canopy recruitment in five tree species from a seasonal tropical forest in western Thailand. J Trop Ecol 22:521–529CrossRefGoogle Scholar
  2. Baker TR et al (2004) Increasing biomass in Amazonian forest plots. Philos Trans R Soc Lond B Biol Sci 359:353–365PubMedCentralPubMedCrossRefGoogle Scholar
  3. Baker PJ, Bunyavejchewin S, Oliver CD, Ashton PS (2005) Disturbance history and historical stand dynamics of a seasonal tropical forest in western Thailand. Ecol Monogr 75:317–343CrossRefGoogle Scholar
  4. Biondi F, Waikul K (2004) DENDROCLIM2002: a C++ program for statistical calibration of climate signals in tree-ring chronologies. Comput Geosci 30:303–311CrossRefGoogle Scholar
  5. Brando PM, Nepstad DC, Davidson EA, Trumbore SE, Ray D, Camargo P (2008) Drought effects on litterfall, wood production and belowground carbon cycling in an Amazon forest: results of a throughfall reduction experiment. Philos Trans R Soc Lond B Biol Sci 363:1839–1848PubMedCentralPubMedCrossRefGoogle Scholar
  6. Brienen RJW, Zuidema PA (2005) Relating tree growth to rainfall in Bolivian rain forests: a test for six species using tree ring analysis. Oecologia 146:1–12PubMedCrossRefGoogle Scholar
  7. Brienen RJW, Lebrija-Trejos E, Zuidema PA, Martínez-Ramos M (2010) Climate–growth analysis for a Mexican dry forest tree shows strong impact of sea surface temperatures and predicts future growth declines. Glob Change Biol 16:2001–2012CrossRefGoogle Scholar
  8. Buckley B, Palakit K, Duangsathaporn K, Sanguantham P, Prasomsin P (2007) Decadal scale droughts over northwestern Thailand over the past 448 years: links to the tropical Pacific and Indian Ocean sectors. Clim Dyn 29:63–71CrossRefGoogle Scholar
  9. Bunn AG (2008) A dendrochronology program library in R (dplR). Dendrochronologia 26:115–124CrossRefGoogle Scholar
  10. Bunyavejchewin S, Baker PJ, Lafrankie JV, Ashton PS (2001) Stand structure of a seasonal dry evergreen forest at Huai Kha Khaeng Wildlife Sanctuary, Western Thailand. Nat Hist Bull Soc 49:89–106Google Scholar
  11. Bunyavejchewin S, LaFrankie JV, Baker PJ, Davies SJ, Ashton PS (2009) Forest trees of Huai Kha Khaeng Wildlife Sanctuary, Thailand: data from the 50-hectare Forest Dynamics Plot. National Parks, Wildlife and Plant Conservation Department, BangkokGoogle Scholar
  12. Choat B et al (2012) Global convergence in the vulnerability of forests to drought. Nature 491:752–755PubMedGoogle Scholar
  13. Clark DA (2004) Sources or sinks? The responses of tropical forests to current and future climate and atmospheric composition. Philos Trans R Soc Lond B Biol Sci 359:477–491PubMedCentralPubMedCrossRefGoogle Scholar
  14. Clark DA (2007) Detecting tropical forests’ responses to global climatic and atmospheric change: current challenges and a way forward. Biotropica 39:4–19CrossRefGoogle Scholar
  15. Clark DA, Piper SC, Keeling CD, Clark DB (2003) Tropical Rain forest tree growth and atmospheric carbon dynamics linked to interannual temperature variation during 1984–2000. Proc Natl Acad Sci USA 100:5852–5857PubMedCentralPubMedCrossRefGoogle Scholar
  16. Clark DB, Clark DA, Oberbauer SF (2010) Annual wood production in a tropical rain forest in NE Costa Rica linked to climatic variation but not to increasing CO2. Glob Change Biol 16:747–759CrossRefGoogle Scholar
  17. Clark DA, Clark DB, Oberbauer SF (2013) Field-quantified responses of tropical rainforest aboveground productivity to increasing CO2 and climatic stress, 1997–2009. J Geophys Res Biogeosci 118:783–794CrossRefGoogle Scholar
  18. Cook E, Briffa K, Shiyatov S, Mazepa V, Jones PD (1990) Data analysis. In: Cook ER, Kairiukstis LA (eds) Methods of dendrochronology. Kluwer, Dordrecht, pp 97–162CrossRefGoogle Scholar
  19. Cook ER, Anchukaitis KJ, Buckley BM, D’Arrigo RD, Jacoby GC, Wright WE (2010) Asian monsoon failure and megadrought during the last millennium. Science 328:486–489PubMedCrossRefGoogle Scholar
  20. Corlett RT (2011) Impacts of warming on tropical lowland rainforests. Trends Ecol Evol 26:606–613PubMedCrossRefGoogle Scholar
  21. Couralet C, Sterck FJ, Sass-Klaassen U, Van Acker J, Beeckman H (2010) Species-specific growth responses to climate variations in understory trees of a central African rain forest. Biotropica 42:503–511CrossRefGoogle Scholar
  22. Denslow JS (1980) Gap partitioning among tropical rainforest trees. Biotropica 12:47–55CrossRefGoogle Scholar
  23. Devall MS, Parresol BR, Wright SJ (1995) Dendrochronological analysis of Cordia alliodora, Pseudobombax septenatum and Annona spraguei in central Panama. IAWA J 16:411–424CrossRefGoogle Scholar
  24. Dixon RK, Solomon AM, Brown S, Houghton RA, Trexier MC, Wisniewski J (1994) Carbon pools and flux of global forest ecosystems. Science 263:185–190PubMedCrossRefGoogle Scholar
  25. Dong SX et al (2012) Variability in solar radiation and temperature explains observed patterns and trends in tree growth rates across four tropical forests. Proc R Soc Lond B Biol Sci 279:3923–3931CrossRefGoogle Scholar
  26. Doughty CE (2011) An in situ leaf and branch warming experiment in the Amazon. Biotropica 43:658–665CrossRefGoogle Scholar
  27. Druckenbrod DL, Pederson N, Rentch J, Cook ER (2013) A comparison of times series approaches for dendroecological reconstructions of past canopy disturbance events. For Ecol Manag 302:23–33CrossRefGoogle Scholar
  28. Dujesiefken D, Rhaesa A, Eckstein D, Stobbe H (1999) Tree wound reactions of differently treated boreholes. J Arboric 25:113–123Google Scholar
  29. Dünisch O, Montóia VR, Bauch J (2003) Dendroecological investigations on Swietenia macrophylla King and Cedrela odorata L. (Meliaceae) in the central Amazon. Trees Struct Funct 17:244–250Google Scholar
  30. Feeley KJ, Joseph Wright S, Nur Supardi MN, Kassim AR, Davies SJ (2007) Decelerating growth in tropical forest trees. Ecol Lett 10:461–469PubMedCrossRefGoogle Scholar
  31. Galbraith D et al (2010) Multiple mechanisms of Amazonian forest biomass losses in three dynamic global vegetation models under climate change. New Phytol 187:647–665PubMedCrossRefGoogle Scholar
  32. Hansen J, Sato M, Ruedy R (2012) Perception of climate change. Proc Natl Acad Sci USA 109:E2415–E2423PubMedCentralPubMedCrossRefGoogle Scholar
  33. Hietz P, Wanek W, Dünisch O (2005) Long-term trends in cellulose δ13C and water-use efficiency of tropical Cedrela and Swietenia from Brazil. Tree Physiol 25:745–752PubMedCrossRefGoogle Scholar
  34. Holmes RL (1983) Computer-assisted quality control in tree-ring dating and measurement. Tree ring Bull 43:69–78Google Scholar
  35. IPCC (2007) Climate Change 2007: the physical science basis. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge University Press, Cambridge, New YorkGoogle Scholar
  36. Jacoby GC (1989) Overview of tree-ring analysis in tropical regions. IAWA Bull 10:99–108CrossRefGoogle Scholar
  37. Kalinganire A, Pinyopusarek K (2000) Chukrasia: biology cultivation and utilisation ACIAR techinical report series. CSIRO Forestry and Forest Products, KingstonGoogle Scholar
  38. Körner C (2003) Carbon limitation in trees. J Ecol 91:4–17CrossRefGoogle Scholar
  39. Körner C (2009) Responses of humid tropical trees to rising CO2. Annu Rev Ecol Evol Syst 40:61–79CrossRefGoogle Scholar
  40. LaFrankie JV (2010) Trees of tropical Asia. Black Tree, PhilippinesGoogle Scholar
  41. Lee TD, Reich PB, Bolstad PV (2005) Acclimation of leaf respiration to temperature is rapid and related to specific leaf area, soluble sugars and leaf nitrogen across three temperate deciduous tree species. Funct Ecol 19:640–647CrossRefGoogle Scholar
  42. Lloyd J, Farquhar GD (1996) The CO2 dependence of photosynthesis, plant growth responses to elevated atmospheric CO2 concentrations and their interaction with soil nutrient status. I. General principles and forest ecosystems. Funct Ecol 10:4–32CrossRefGoogle Scholar
  43. Lloyd J, Farquhar GD (2008) Effects of rising temperatures and [CO2] on the physiology of tropical forest trees. Philos Trans R Soc Lond B Biol Sci 363:1811–1817PubMedCentralPubMedCrossRefGoogle Scholar
  44. Loader NJ et al (2011) Recent trends in the intrinsic water-use efficiency of ringless rainforest trees in Borneo. Philos Trans R Soc Lond B Biol Sci 366:3330–3339PubMedCentralPubMedCrossRefGoogle Scholar
  45. Malhi Y, Grace J (2000) Tropical forests and atmospheric carbon dioxide. Trends Ecol Evol 15:332–337PubMedCrossRefGoogle Scholar
  46. Marcott SA, Shakun JD, Clark PU, Mix AC (2013) A reconstruction of regional and global temperature for the past 11,300 years. Science 339:1198–1201PubMedCrossRefGoogle Scholar
  47. Meir P, Metcalfe DB, Costa ACL, Fisher RA (2008) The fate of assimilated carbon during drought: impacts on respiration in Amazon rainforests. Philos Trans R Soc Lond B Biol Sci 363:1849–1855PubMedCentralPubMedCrossRefGoogle Scholar
  48. Metcalfe DB et al (2010) Shifts in plant respiration and carbon use efficiency at a large-scale drought experiment in the eastern Amazon. New Phytol 187:608–621PubMedCrossRefGoogle Scholar
  49. Nghia NH (1998) Afzelia xylocarpa IUCN 2011. IUCN Red List of Threatened Species. IUCN, CambridgeGoogle Scholar
  50. Nguyen NC et al (1996) Vietnam forest trees. Agricultural Publishing House, HanoiGoogle Scholar
  51. Nock CA et al (2011) Long-term increases in intrinsic water-use efficiency do not lead to increased stem growth in a tropical monsoon forest in western Thailand. Glob Change Biol 17:1049–1063CrossRefGoogle Scholar
  52. Ohashi S, Okada N, Nobuchi T, Siripatanadilok S, Veenin T (2009) Detecting invisible growth rings of trees in seasonally dry forests in Thailand: isotopic and wood anatomical approaches. Trees Struct Funct 23:813–822CrossRefGoogle Scholar
  53. Oliver CD, Larson BC (1996) Forest stand dynamics. Wiley, New YorkGoogle Scholar
  54. Pederson N, Cook ER, Jacoby GC, Peteet DM, Griffin KL (2004) The influence of winter temperatures on the annual radial growth of six northern range margin tree species. Dendrochronologia 22:7–29CrossRefGoogle Scholar
  55. Pinheiro J, Bates D, DebRoy S, Sarkar D, the R Development Core Team (2011) nlme: linear and nonlinear mixed effects models, R package version 3.1–101 edn Google Scholar
  56. Poussart PF, Evans MN, Schrag DP (2004) Resolving seasonality in tropical trees: multi-decade, high-resolution oxygen and carbon isotope records from Indonesia and Thailand. Earth Planet Sci Lett 218:301–316CrossRefGoogle Scholar
  57. Pumijumnong N (2012) Dendrochronology in Southeast Asia. Trees Struct Funct 27:343–358CrossRefGoogle Scholar
  58. Pumijumnong N, Eckstein D, Sass U (1995) Tree-ring research on Tectona grandis in Northern Thailand. IAWA J 16:385–392CrossRefGoogle Scholar
  59. R Core Development Team (2013) R: a language and environment for statistical computing, 3.0.0 edn. R Foundation for Statistical Computing, Vienna, AustriaGoogle Scholar
  60. Rozendaal DMA, Zuidema PA (2011) Dendroecology in the tropics: a review. Trees Struct Funct 25:3–16CrossRefGoogle Scholar
  61. Schöngart J, Orthmann B, Hennenberg KJ, Porembski S, Worbes M (2006) Climate–growth relationships of tropical tree species in West Africa and their potential for climate reconstruction. Glob Change Biol 12:1139–1150CrossRefGoogle Scholar
  62. Soliz-Gamboa C, Rozendaal DA, Ceccantini G, Angyalossy V, Borg K, Zuidema P (2011) Evaluating the annual nature of juvenile rings in Bolivian tropical rainforest trees. Trees Struct Funct 25:17–27CrossRefGoogle Scholar
  63. Speer JH (2010) Fundamentals of tree-ring research. University of Arizona Press, TucsonGoogle Scholar
  64. Stokes MA, Smiley TL (1968) An introduction to tree-ring dating. University of Chicago, ChicagoGoogle Scholar
  65. Trouet V, Van Oldenborgh GJ (2013) KNMI climate explorer: a web-based research tool for high-resolution paleoclimatology. Tree Ring Res 69:3–13CrossRefGoogle Scholar
  66. Wang B, Ho L (2002) Rainy season of the Asian-Pacific summer monsoon. J Clim 15:386–398CrossRefGoogle Scholar
  67. Wigley TM, Briffa KR, Jones PD (1984) On the average value of correlated time series, with applications in dendroclimatology and hydrometeorology. J Clim Appl Meteorol 23:201–213CrossRefGoogle Scholar
  68. Williams LJ, Bunyavejchewin S, Baker PJ (2008) Deciduousness in a seasonal tropical forest in western Thailand: interannual and intraspecific variation in timing, duration and environmental cues. Oecologia 155:571–582PubMedCrossRefGoogle Scholar
  69. Worbes M (1995) How to measure growth dynamics in tropical trees a review. IAWA J 16:337–351CrossRefGoogle Scholar
  70. Worbes M (2002) One hundred years of tree-ring research in the tropics—a brief history and an outlook to future challenges. Dendrochronologia 20:217–231CrossRefGoogle Scholar
  71. Worbes M, Junk WJ (1989) Dating tropical trees by means of 14C from bomb tests. Ecology 70:503–507CrossRefGoogle Scholar
  72. Wright SJ, Muller-Landau HC, Schipper JAN (2009) The future of tropical species on a warmer planet. Conserv Biol 23:1418–1426PubMedCrossRefGoogle Scholar
  73. Zang C, Biondi F (2013) Dendroclimatic calibration in R: the bootRes package for response and correlation function analysis. Dendrochronologia 31:68–74CrossRefGoogle Scholar
  74. Zuidema PA, Vlam M, Chien PD (2011) Ages and long-term growth patterns of four threatened Vietnamese tree species. Trees Struct Funct 25:29–38CrossRefGoogle Scholar
  75. Zuidema PA, Brienen RJW, Schöngart J (2012) Tropical forest warming: looking backwards for more insights. Trends Ecol Evol 27:193–194PubMedCrossRefGoogle Scholar
  76. Zuidema PA, Baker PJ, Groenendijk P, Schippers P, van der Sleen P, Vlam M, Sterck F (2013) Tropical forests and global change: filling knowledge gaps. Trends Plant Sci 18:1360–1385CrossRefGoogle Scholar
  77. Zuur AF, Ieno EN, Walker NJ, Savaliev AA, Smith GM (2009) Mixed effects models and etensions in ecology with R. Springer, New YorkCrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  • Mart Vlam
    • 1
  • Patrick J. Baker
    • 2
  • Sarayudh Bunyavejchewin
    • 3
  • Pieter A. Zuidema
    • 1
  1. 1.Forest Ecology and Forest Management GroupWageningen UniversityWageningenThe Netherlands
  2. 2.Department of Forest and Ecosystem ScienceUniversity of MelbourneVictoriaAustralia
  3. 3.Department of National Parks, Wildlife and Plant ConservationBangkokThailand

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