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Ficus benjamina L. (1767)
by Mrs. Thivya Laxshmy Raman
Newsletter
Ficus benjamina L. (1767)
by Mrs. Thivya Laxshmy Raman

In the canopies of primary forests and urban forests, the Weeping Fig (Ficus benjamina) is among the most intricate living things found in Malaysia. This species is more than just an ornamental plant; it is an ecosystem engineer that balances biodiversity through dynamic survival strategies (Ross et al., 2020). An evergreen member of the Moraceae family, it can reach heights of up to 30 meters. This species belongs to the category of hemiepiphytes, organisms that spend part of their life as epiphytes on another tree (Berg & Corner, 2005).

The diameter at breast height (DBH) of Ficus benjamina is usually between 30 cm and 60 cm. However, due to lignification, they form a compound trunk that can reach several meters in width when their aerial roots fuse. This structure provides extraordinary mechanical stability, enabling them to support a massive canopy. A critical morphological feature is the presence of white latex containing the enzyme ficin (Devaraj et al., 2008). This biochemical substance serves as a sticky, toxic chemical defence mechanism against most herbivorous insects, protecting the integrity of the tree's tissues from pest attacks (Devaraj et al., 2008).

The altitudinal range of Ficus benjamina is wide, ranging from the coast to lowland forests up to 1,300 meters above sea level. The plant's life cycle begins with seed dispersal by frugivorous animals, which carries the seeds into the plant's high tall canopy, which are 20 to 40 meters high (Laman, 1995). These plants have aerial roots that help absorb moisture directly from the humid forest atmosphere (Zimmermann et al., 1968), thereby maintaining humidity levels of 70% to 90%. This process slowly constricts the host's secondary growth and phloem (nutrient-transporting tissue), causing the host to rot and leaving a hollow core in the centre of the Fig tree (Hao et al., 2016).

Ecologically, the Ficus is considered a keystone species due to its asynchronous fruiting (Shanahan et al., 2001). Compared to the Dipterocarp tree species, which have fruits produced during masting years, Ficus benjamina can produce fruits all year round (Zainuddin & Payne, 2022). The fruits of the plant are very small, ranging from 2.0 cm to 2.5 cm. During lean seasons in the forest, the Fig becomes the sole source of energy for the survival of hornbills, primates and bats.

This mode of reproduction occurs through a symbiotic relationship with a fig wasp known as Eupristina verticillata (Zainuddin & Payne, 2022). The flowers inside the syconium (fruit's inner part) can be pollinated only by these micro-wasps that enter through the ostiole (small hole) (Zainuddin & Payne, 2022). Without this particular symbiosis, the life cycles of both organisms would come to a halt (Zainuddin & Payne, 2022).

Despite being commonly regarded as a threat to urban structures, Ficus benjamina provides many ecosystem services. Studies show that the plant is highly effective at removing air pollutants such as formaldehyde and xylene (Kim et al., 2008). Additionally, its vast canopy enables high carbon sequestration rates, while evapotranspiration effectively lowers micro temperatures in urban environments (Yang et al., 2026).

The conservation status of Ficus benjamina in Malaysia is classified as "Least Concern". However, it must not be underplayed given its role as a heart of biodiversity. The danger lies not in the extinction of the species but rather in the diminishing pollinator population associated with the plant (Harrison, 2005). By saving the Fig tree, an intricate network of life in our rainforests is maintained.

References

  1. Berg, C.C. & Corner, E.J.H. (2005). Moraceae: Ficeae. Flora Malesiana-Series 1, Spermatophyta. In Nooteboom, H.P., Berg, C.C. & Corner, E.J.H. (Eds.), Flora Malesiana. Series 1 - Seed Plants, Moraceae - Ficus, Volume 17 (2). Nationaal Herbarium Nederland, Universiteit Leiden branch, The Netherlands. pp. 1-702.
  2. Devaraj, K. B., Kumar, P. R. & Prakash, V. (2008). Purification, characterization and solvent-induced thermal stabilization of ficin from Ficus carica. Journal of Agricultural and Food Chemistry 56 (23), 11417-11423
  3. Hao, G. Y., Cao, K. F. & Goldstein, G (2016). Hemiepiphytic trees: Ficus as a model system for understanding hemiepiphytism. In Tropical Tree Physiology: Adaptations and Responses in a Changing Environment. Cham: Springer International Publishing.
  4. Harrison, R.D. (2005). Figs and the Diversity of Tropical Rainforests. BioScience 55 (12), 1053 - 1064
  5. Kim, K. J., Kil, M. J., Song, J. S., Yoo, E. H., Son, K. C. & Kays, S. J. (2008). Efficiency of volatile formaldehyde removal by indoor plants: contribution of aerial plant parts versus the root zone. Journal of the American Society for Horticultural Science 133 (4), 521-526
  6. Laman, T. G. (1995). The ecology of strangler fig seedling establishment. Selbyana, 223-229
  7. Ross, C. E., McIntyre, S., Barton, P. S., Evans, M. J., Cunningham, S. A. & Manning, A. D. (2020). A reintroduced ecosystem engineer provides a germination niche for native plant species. Biodiversity and Conservation 29 (3), 817-837
  8. Yang, X., Li, B., Li, N. & Ma, X. (2026). A study of the cooling effect of urban trees: Influencing factors, assessment methods, planning strategies, and impacts. Theoretical and Applied Climatology 157 (1), 31. https://doi.org/10.1007/s00704-025-05904-2
  9. Zainuddin, Z.Z. & Payne, J. (2022). Sabah Ficus Germplasm Centre (SFGC), Tabin Wildlife Reserve, Sabah. Malayan Nature Journal 74 (3), 401-405
  10. Zimmermann, M. H., Wardrop, A. B. & Tomlinson, P. B. (1968). Tension wood in aerial roots of Ficus benjamina L. Wood Science and Technology 2 (2), 95-104
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