STRUCTURAL AND COMPOSITIONAL REORGANIZATION IN PERMANENT CAATINGA PLOTS: EVIDENCE OF COMPENSATORY GROWTH AND REDISTRIBUTION OF DOMINANCE BETWEEN 2022 AND 2024
DOI:
https://doi.org/10.66104/pnmen722Keywords:
Caatinga, Dry forest, Forest inventory, Permanent plotsAbstract
Seasonally dry tropical forests exhibit dynamics that are strongly modulated by climatic variability and water stress, factors that simultaneously influence mortality, growth, and species composition. This study evaluated structural and compositional changes in 32 permanent plots located in the Caatinga, Northeastern Brazil, by comparing forest inventories conducted in 2022 and 2024. Variations in stem density (N), basal area (G), diameter distribution, species-specific contribution to structural increment (ΔG), Bray–Curtis dissimilarity, and multivariate patterns through NMDS ordination were analyzed.
A slight reduction in mean density per plot was observed, accompanied by a marked increase in basal area, indicating compensatory growth of the remaining individuals. Diameter class distribution showed a decline in the smallest class and an increase in intermediate classes, suggesting structural progression with limited recruitment during the study period. Basal area increment was concentrated in a few species, particularly Prosopis juliflora and Poincianella pyramidalis, indicating a reorganization of structural dominance. Dissimilarities were higher when based on basal area than on abundance, revealing stronger changes in biomass structure than in floristic composition. NMDS ordination revealed heterogeneous shifts among plots, suggesting locally differentiated responses.
The results indicate that, during the analyzed interval, the community exhibited significant structural growth accompanied by a reorganization of dominance, a pattern consistent with recent processes described for Latin American dry forests under climatic variability.
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ANDRADE, L. A.; FABRICANTE, J. R.; OLIVEIRA, F. X. Invasão biológica por Prosopis juliflora (Sw.) DC.: impactos sobre a diversidade e a estrutura do componente arbustivo-arbóreo da caatinga no estado do Rio Grande do Norte, Brasil. Acta Botanica Brasilica, v. 23, n. 4, p. 935–943, 2009. DOI: https://doi.org/10.1590/S0102-33062009000400004 DOI: https://doi.org/10.1590/S0102-33062009000400004
BÁEZ, S.; COLLINS, S. L.; POCKMAN, W. T.; JOHNSON, J. E.; SMALL, E. E. Effects of experimental rainfall manipulations on Chihuahuan Desert grassland and shrubland plant communities. Oecologia, v. 172, n. 4, p. 1117–1127, 2013. DOI: https://doi.org/10.1007/s00442-012-2552-0 DOI: https://doi.org/10.1007/s00442-012-2552-0
BELLINGHAM, P. J.; SPARROW, A. D. Resprouting as a life history strategy in woody plant communities. Oikos, v. 89, n. 2, p. 409–416, 2000. DOI: https://doi.org/10.1034/j.1600-0706.2000.890224.x DOI: https://doi.org/10.1034/j.1600-0706.2000.890224.x
CLARKE, K. R.; TWEEDLEY, J. R.; VALESINI, F. J. Simple shade plots aid better long-term choices of data pre-treatment in multivariate assemblage studies. Journal of the Marine Biological Association of the United Kingdom, v. 94, n. 1, p. 1–16, 2014. DOI: https://doi.org/10.1017/S0025315413001227 DOI: https://doi.org/10.1017/S0025315413001227
DANTAS, V. L.; PAUSAS, J. G.; BATALHA, M. A.; LOIOLA, P. P.; CIANCIARUSO, M. V. Climate control of leaf traits and wood density in seasonally dry tropical forests. Forest Ecology and Management, v. 432, p. 79 – 86, 2019.
ESQUIVEL-MUELBERT, A. et al. Compositional response of Amazon forests to climate change. Global Change Biology, v. 25, n. 1, p. 39–56, 2019. DOI: https://doi.org/10.1111/gcb.14413 DOI: https://doi.org/10.1111/gcb.14413
KORNING, J.; BALSLEV, H. Growth and mortality of trees in Amazonian tropical rain forest in Ecuador. Journal of Vegetation Science, v. 5, n. 1, p. 77–86, 1994. DOI: https://doi.org/10.2307/3235641 DOI: https://doi.org/10.2307/3235641
LEWIS, S. L. et al. Concerted changes in tropical forest structure and dynamics: evidence from 50 South American long-term plots. Philosophical Transactions of the Royal Society B, v. 359, n. 1443, p. 421–436, 2004. DOI: https://doi.org/10.1098/rstb.2003.1431 DOI: https://doi.org/10.1098/rstb.2003.1431
MA, Z. et al. Regional drought-induced reduction in the biomass carbon sink of Canada's boreal forests. Proceedings of the National Academy of Sciences, v. 109, n. 7, p. 2423–2427, 2016. DOI: https://doi.org/10.1073/pnas.1111576109 DOI: https://doi.org/10.1073/pnas.1111576109
MAO, Q. et al. Responses of understory plant physiological traits to a decade of nitrogen addition in a tropical reforested ecosystem. Forest Ecology and Management, v. 401, p. 65–74, 2017. DOI: https://doi.org/10.1016/j.foreco.2017.06.047 DOI: https://doi.org/10.1016/j.foreco.2017.06.047
MARENGO, J. A.; TORRES, R. R.; ALVES, L. M. Drought in Northeast Brazil—past, present, and future. Theoretical and Applied Climatology, v. 129, p. 1189–1200, 2017. DOI: https://doi.org/10.1007/s00704-016-1840-8 DOI: https://doi.org/10.1007/s00704-016-1840-8
MARLINE, L.; AH-PENG, C.; HEDDERSON, T. A. J. Epiphytic bryophyte diversity and range distributions along an elevational gradient in Marojejy, Madagascar. Biotropica, v. 52, p. 1–11, 2020. DOI: https://doi.org/10.1111/btp.12781 DOI: https://doi.org/10.1111/btp.12781
MARTÍNEZ-RAMOS, M. et al. Natural forest regeneration and ecological restoration in human-modified tropical landscapes. Ecology, v. 99, n. 1, p. 36–47, 2018. DOI: https://doi.org/10.1111/btp.12382 DOI: https://doi.org/10.1111/btp.12382
PHILLIPS, O. L. et al. Drought sensitivity of the Amazon rainforest. Science, v. 323, n. 5919, p. 1344–1347, 2009. DOI: https://doi.org/10.1126/science.1164033 DOI: https://doi.org/10.1126/science.1164033
PHILLIPS, O. L.; HALL, P.; GENTRY, A. H.; SAWYER, S. A.; VÁSQUEZ, R. Dynamics and species richness of tropical rain forests. Proceedings of the National Academy of Sciences, v. 91, n. 7, p. 2805–2809, 1994. DOI: https://doi.org/10.1073/pnas.91.7.2805 DOI: https://doi.org/10.1073/pnas.91.7.2805
POORTER, L. et al. Biomass resilience of Neotropical secondary forests. Nature, v. 530, n. 7589, p. 211–214, 2016. DOI: https://doi.org/10.1038/nature16512 DOI: https://doi.org/10.1038/nature16512
PRATHER, C. M.; BELOVSKY, G. E.; CANTRELL, S. A.; GONZÁLEZ, G. Tropical herbivorous phasmids, but not litter snails, alter decomposition rates by modifying litter bacteria. Ecology, v. 99, n. 4, p. 782–791, 2018. DOI: https://doi.org/10.1002/ecy.2169 DOI: https://doi.org/10.1002/ecy.2169
SÁENZ-PEDROZA, I. et al. Seasonal drought drives tree mortality and recruitment in a tropical dry forest. Journal of Vegetation Science, v. 31, n. 3, p. 420–431, 2020. DOI: https://doi.org/10.7717/peerj.9636 DOI: https://doi.org/10.7717/peerj.9636
SHEIL, D.; BURSLEM, D. F. R. P.; ALDER, D. The interpretation and misinterpretation of mortality rate measures. Journal of Ecology, v. 83, n. 2, p. 331–333, 1995. DOI: https://doi.org/10.2307/2261571 DOI: https://doi.org/10.2307/2261571
SILVA, J. M. C.; LEAL, I. R.; TABARELLI, M. Caatinga: the largest tropical dry forest region in South America. Forest Ecology and Management, v. 400, p. 1–3, 2017. DOI: https://doi.org/10.1007/978-3-319-68339-3 DOI: https://doi.org/10.1007/978-3-319-68339-3
VIEIRA, R. M. S. P. et al. Identifying areas susceptible to desertification in the Brazilian northeast. Solid Earth, v. 6, p. 347–360, 2015. DOI: https://doi.org/10.5194/se-6-347-2015 DOI: https://doi.org/10.5194/se-6-347-2015
VILANOVA, E. et al. Environmental drivers of forest structure and stem turnover across Venezuelan tropical forests. PLOS ONE, v. 13, n. 6, e0198489, 2018. DOI: https://doi.org/10.1371/journal.pone.0198489 DOI: https://doi.org/10.1371/journal.pone.0198489
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Copyright (c) 2026 Cleyton dos Santos Souza, Leandro Nicholas Albuquerque Silva, Sara Sebastiana Nogueira, Maria Gabriela do Nascimento, Elaine Cristina Alves da Silva , Jacqueline Wanessa de Lima Pereira, Maria José de Holanda Leite, Átila Bruno de Moraes Almeida, Rosilvam Ramos de Sousa, Maria Janaina Nascimento Silva

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