Abstract
Plants release secondary metabolites into the soil that change the chemical environment around them. Exogenous abscisic acid (ABA) is an important allelochemical whose role in successional trajectories has not been examined. We hypothesized that ABA can accumulate in the soil through successional processes and have an influence on forest dynamics. To this end, we investigated the distribution of ABA in forest communities from early to late successional stages and the response of dominant species to the gradient of ABA concentrations in three types of forests from northern to southern China. Concentrations of ABA in the soils of three forest types increased from early to late successional stages. Pioneer species’ litters had the lowest ABA content, and their seed germination and seedling early growth were the most sensitive to the inhibitory effect of ABA. Mid- and late-successional species had a much higher ABA content in fallen leaves than pioneer species, and their seed germination and seedling early growth were inhibited by higher concentrations of ABA than pioneers. Late-successional species showed little response to the highest ABA concentration, possibly due to their large seed size. The results suggest that ABA accumulates in the soil as community succession proceeds. Sensitivity to ABA in the early stages, associated with other characteristics, may result in pioneer species losing their advantage in competition with late-successional species in an increasingly high ABA concentration environment, and being replaced by ABA-tolerant, late-successional species.
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Amaral Da Silva, E. A., Toorop, P. E., Van Lammeren, A. A. M., and Hilhorst, H. W. M. 2008. ABA inhibits embryo cell expansion and early cell division events during coffee (Coffea arabica ‘Rubi’) seed germination. Ann. Bot-London 102:425–433.
Anderson, R. C., Katz, A. J., and Anderson, M. R. 1978. Allelopathy as a factor in the success of Helianthus mollis Lam. J. Chem. Ecol. 4:9–16.
Bartha, S. 2001. Spatial relationships between plant litter, gopher disturbance and vegetation at different stages of old-field succession. Appl. Veg. Sci. 4:53–62.
Bosy, J. L., and Reader, R. J. 1995. Mechanisms underlying the suppression of forb seedling emergence by grass (Poa pratensis) litter. Funct. Ecol. 9:635–639.
Buta, J. G., and Spaulding, D. W. 1989. Allelochemicals in tall fescue-abscisic and phenolic acids. J. Chem. Ecol. 15:1629–1636.
Chobot, V., and Hadacek, F. 2009. Milieu-Dependent Pro- and Antioxidant Activity of Juglone May Explain Linear and Nonlinear Effects on Seedling Development. J. Chem. Ecol. 35:383–390.
Chung, I. M., Ahn, J. K., and Yun, S. J. 2001. Assessment of allelopathic potential of barnyard grass (Echinochloa crusalli) on rice (Oryza sativa L.) cultivars. Crop Prot. 20:921–928.
Coley, P. D., Bryant, J. P., and Chapin, F. S. 1985. Resource availability and plant antiherbivore defense. Science 230:895–899.
Cortez, J., Garnier, E., Perez-harguindeguy, N., Debussche, M., and Gillon, D. 2007. Plant traits, litter quality and decomposition in a Mediterranean old-field succession. Plant Soil 296:19–34.
Facelli, J. M. 1994. Multiple indirect effects of plant litter affect the establishment of woody seedlings in old fields. Ecology 75:1727–1735.
Facelli, J. M., and Kerrigan, R. 1996. Effects of ash and four types of litter the establishment of Eucalyptus obliqua. Ecoscience 3:319–324.
Facelli, J. M., and Pickett, S. T. A. 1991a. Plant litter: its dynamics and effects on plant community structure. Bot. Rev. 57:1–32.
Facelli, J. M., and Pickett, S. T. A. 1991b. Plant litter: light interception and effects on an old-field plant community. Ecology 72:1024–1031.
Fernandez, C., Lelong, B., Vila, B., Mévy, J. P., Robles, C., Greff, S., Dupouyet, S., and Anne, B. M. 2006. Potential allelopathic effect of Pinus halepensis in the secondary succession: an experimental approach. Chemoecology 16:97–105.
Finkelstein, R. R., Gampala, S. S. L., and Rock, C. D. 2002. Abscisic acid signaling in seeds and seedlings. Plant Cell 14:15–45.
Foster, B. L. 1999. Establishment, competition and the distribution of native grasses among Michigan old-fields. J. Ecol. 87:476–489.
Ganade, G., and Brown, V. K. 2002. Succession in old pastures of central amazonia: role of soil fertility and plant litter. Ecology 3:743–754.
Gao, Q., Peng, S. L., Zhao, P., Zeng, X. P., Cai, X., Yu, M., Shen, W. J., and Liu, Y. H. 2003. Explanation of vegetation succession in subtropical southern China based on ecophysiological characteristics of plant species. Tree Physiol. 9:641–648.
Goldberg, D. E., and Werner, P. A. 1983. The effects of size of opening in vegetation and litter cover on seedling establishment of goldenrods (Solidago ssp.). Oecologia 60:149–155.
Grime, J. P., Mason, G., Curtis, A. V., Rodman, J., Band, S. R., Mowforth, M. A. G., Neal, A. M., and Shaw, S. 1981. A comparative study of germination characteristics in a local flora. J. Ecol. 69:1017–1059.
Hattenschwiler, S., and Vitousek, P. M. 2000. The role of polyphenols in terrestrial ecosystem nutrient cycling. Trends Ecol. Evol. 15:238–243.
Hester, A. J., Gimingham, C. H., and Miles, J. 1991. Succession from heather moorland to birch woodland.III. seed availability, germination and early growth. J. Ecol. 79:329–344.
Hocher, V., Sotta, B., Maldiney, R., and Miginiac, E. 1991. Changes in abscisic acid and its β-D-glucopyranosyl ester levels during tomato (Lycopersicon esculentum Mill.) seed development. Plant Cell Rep. 10:444–447.
Jensen, K., and Gutekunst, K. 2003. Effects of litter on establishment of grassland plant species: the role of seed size and successional status. Basic Appl. Ecol. 4:579–587.
Jensen, K., and Schrautzer, J. 1999. Consequences of abandonment for a regional fen flora and mechanisms of successional change. Appl. Veg. Sci. 2:79–88.
Kardol, P., Bezemer, T. M., and Van Der Putten, W. H. 2006. Temporal variation in plant-soil feedback controls succession. Ecol. Lett. 9:1080–1088.
Koegel-knabner, I., Hatcher, P. G., and Zech, W. 1991. Chemical structural studies of forest soil humic acids aromatic carbon fraction. Soil Sci. Soc. Am. J. 55:241–247.
Kröpelin, S., Verschuren, D., Lézine, A. M., Eggermont, H., Cocquyt, C., Francus, P., Cazet, J. P., Fagot, M., Rumes, B., Russell, J. M., Darius, F., Conley, D. J., Schuster, M., Von Suchodoletz, H., and Engstrom, D. R. 2008. Climate-driven ecosystem succession in the sahara: the past 6000 years. Science 320:765–768.
Leishman, M. R., and Westoby, M. 1994. The role of large seed size in shaded conditions: experimental evidence. Funct. Ecol. 8:205–214.
Leung, J., and Giraudat, J. 1998. Abscisic acid signal transduction. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49:199.
Monk, C. D., and Gabrielson, F. C. 1985. Effect of shade, litter and root competition on old field vegetation in South Carolina. Bull. Torrey Bot. Club 112:383–392.
Mowha, J. A., and Jackson, D. L. 1976. Some growth promotive effects of abscisic acid. J. Exp. Bot. 100:1004–1008.
Northup, R. R., Dahlgren, R. A., and Mccoll, J. G. 1998. Polyphenols as regulators of plant-litter-soil interactions in northern California’s pygmy forest: a positive feedback? Biogeochemistry 42:189–220.
Ostertag, R., Marin-spiotta, E., Silver, W. L., and Schulten, J. 2008. Litterfall and decomposition in relation to soil carbon pools along a secondary forest chronosequence in Puerto Rico. Ecosystems 11:701–714.
Pelèse, F., Megnegneau, B., Sotta, B., Sossountzov, L., Caboche, M., and Miginiac, E. 1989. Hormonal characterization of a nonrooting naphthalene-acetic acid tolerant tobacco tutant by an immunoenzymic method. Plant Physiol. 89:86–92.
Pilet, P. E., and Saucy, M. 1987. Effect on root growth of endogenous and applied IAA and ABA. Plant Physiol. 83:33–38.
Reigosa, M. J., Sanchez-moreiras, A., and Gonzalez, L. 1999. Ecophysiological approach in allelopathy. Crit. Rev. Plant Sci. 18:577–608.
Rice, E. L. 1972. Allelopathic effects of andropogon virginicus and its persistence in old fields. Am. J. Bot. 7:752–755.
Rietveld, W. J., Schelinger, R. C., and Kessler, K. J. 1983. Allelopathic effects of black walnut on European black alder coplanted as a nurse species. J. Chem. Ecol. 9:119–1133.
Ruprecht, E., Donath, T. W., Otte, A., and Eckstein, R. L. 2008. Chemical effects of a dominant grass on seed germination of four familial pairs of dry grassland species. Seed Sci. Res. 18:239–248.
Tilman, D. 1993. Species richness of experimental productivity gradients: how important is colonisation limitation? Ecology 74:2179–2191.
Tseng, M. H., Kuo, Y. H., and Chen, Y. M. 2003. Allelopathic Potential of Macaranga tanarius (L.)MUELL.-ARG. J. Chem. Ecol. 5:1269–1286.
Turnball, L. A., Rees, M., and Crawley, M. J. 1999. Seed mass and the competition/colonisation trade-off: a sowing experiment. J. Ecol. 87:899–912.
Vellend, M., Lechowicz, M. J., and Waterway, M. J. 2000. Germination and establishment of forest sedges (Carex, Cyperaceae): tests for home-site advantage and effects of leaf litter. Am. J. Bot. 87:1517–1525.
Venable, D. L., and Brown, J. S. 1988. The selective interactions of dispersal, dormancy, and seed size as adaptations for reducing risk in variable environments. Am. Nat. 131:361–384.
Wardle, D. A., Nicholson, K. S., and Rahman, A. 1993. Influence of plant age on the allelopathic potential of nodding thistle (Carduus nutans L.) against pasture grasses and legumes. Weed Res. 33:69–78.
Wilby, A., and Brown, V. K. 2001. Herbivory, litter and soil disturbance as determinants of vegetation dynamics during early old-field succession under set-aside. Oecologia 127:259–265.
Acknowledgements
We thank Guanhua Dai, Quan Chao, and Dingsheng Mo for field assistance; Jinrong Wu, Guimin Hu, and Wentian Wang for laboratory analyses. Xiaoyi Wei and Yanjun Du provided very helpful comments on the manuscript. We also thank Anne Bjorkman at the University of British Columbia for assistance with English language and grammatical editing of the manuscript. This research was funded by National Natural Science Foundation of China (NSFC 30670385; U0633002) and basic science foundation of Research Institute of Tropical Forestry, Chinese Academy of Forestry (RITFYWZX200905; CAFYBB2008004).
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Fig. S1
Map of the three experimental forests studied in this paper. (DOC 196 kb)
Table S1
Percentage of seed germination (%) of dominant species of all successional stages in three sample forests on culture with a gradient of ABA concentrations. Data in table are mean percent of germination ± tandard error. Different letters follow significantly different means (P<0.05). (DOC 43 kb)
Table S2
Seedling length (cm) of dominant species of all successional phases in three sample forests on culture with a gradient of ABA concentrations. Data in table are mean seedling length (shoot and root) ± standard error. Different letters follow significantly different means (P<0.05). (DOC 43 kb)
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Zhao, H., Peng, S., Chen, Z. et al. Abscisic Acid in Soil Facilitates Community Succession in Three Forests in China. J Chem Ecol 37, 785–793 (2011). https://doi.org/10.1007/s10886-011-9970-z
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DOI: https://doi.org/10.1007/s10886-011-9970-z