Water Deficit Irrigation of Robusta Coffee Under Nursery Conditions in Sultan Kudarat, Philippines

Authors

  • Rhealiza C. Evasco Provincial Government of South Cotabato, City of Koronadal, South Cotabato, Philippines
  • Junito P. Marcelino Sultan Kudarat State University, EJC Montilla, Tacurong City, Philippines

DOI:

https://doi.org/10.69569/jip.2025.277

Keywords:

Drought stress, Irrigation, Robusta coffee, Water management, Water deficit

Abstract

Robusta Coffee (Coffea canephora) is sensitive to water deficit, and its production is increasingly vulnerable to climate change, requiring the selection of drought-tolerant varieties. The study aimed to evaluate the growth response of four "France de Torino" clones (FRT 07, FRT 11, FRT 23, FRT 65) developed by Nestlé's Research and Development facility and three farmer-selected varieties (FRV-B, FRV-SNA, FRV-K) under stress conditions by withholding irrigation for 7, 14, and 21 days using a completely randomized design (CRD) with factorial treatment combinations. Growth responses were assessed based on leaf scorching, plant height, stem girth, number of leaves, soil moisture content, percentage of plant recovery, and biomass accumulation. Temperature and relative humidity (RH) were monitored to assess microclimatic effects. Results showed that prolonged drought stress reduced plant height (from 43.78 ± 4.21 cm at 7 days to 29.88 ± 3.42 cm at 21 days) and number of leaves (from 28.6 ± 3.4 to 15.8 ± 2.2), and increased leaf scorching (from 5.12 ± 1.38 to 21.32 ± 2.94). Among clones, FRT 23 had the highest average plant height (27.44 cm) under stress, while FRV-SNA exhibited the most incredible resilience across metrics, including the highest recovery rate (91.67%) and biomass accumulation (wet: 37.33 g; dry: 17.83 g). ANOVA revealed that drought stress significantly affected the growth parameters (p < 0.0001), while clone type influenced stem girth and recovery rate. Environmental monitoring revealed that inside the screenhouse, temperature reached a mean of 34.09°C, with relative humidity averaging 67%. Pearson's correlation showed strong inverse relationships between RH and inside screenhouse temperature (r = -0.9279, p < 0.001). Regression analysis indicated that temperature explained 86.1% of RH variability (Adj R² = 0.8605). Plants under 50% shade netting experienced moderated microclimates, supporting better growth under stress. The results were essential to improve the variety selection and water management strategies, ensuring long-term productivity and resilience of coffee in drought-prone areas.

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References

Anim-Kwapong, E., Padi, F. K., & Danquah, E. Y. (2011). Variation and association among characters genetically related to yield and yield stability. Journal of Plant Breeding and Crop Science, 3(12), 311–320. https://doi.org/10.5897/JPBCS11.054

Arunyanark, A., Roonprapant, P., Sridokchan, W., Pakoktom, T., & Chutteang, C. (2022). Effect of water deficit and propagation methods on physiological responses of robusta coffee (Coffea canephora) varieties. Agriculture and Natural Resources, 56(6), 1123–1134. https://doi.org/10.34044/j.anres.2022.56.6.07

Avelino, J., Cristancho, M., Georgiou, S., Imbach, P., Aguilar, L., Bornemann, G., Läderach, P., Anzueto, F., Hruska, A. J., & Morales, C. (2015). The Coffee Rust Crisis in Colombia and Central America (2008–2013): Impacts, plausible causes and proposed solutions. Food Security, 7(2), 303–321. https://doi.org/10.1007/s12571-015-0446-9

Begg, J. E., & Turner, N. C. (1970). Water potential gradients in field tobacco. Plant Physiology, 46(2), 343–346. https://doi.org/10.1104/pp.46.2.343

Boston, R. C., & Sumner, A. E. (2003). STATA: A statistical analysis system for examining biomedical data. In J. A. Novotny, M. H. Green, & R. C. Boston (Eds.), Mathematical modeling in nutrition and the health sciences (Vol. 537, pp. 191–202). Springer. https://doi.org/10.1007/978-1-4419-9019-8_23

Campanha, M.M., Santos, R.H.S., de Freitas, G.B., Martinez, H.E.P., Muniz, J.A., & Finger, F.L. (2004). Growth and yield of coffee plants in agroforestry and monoculture systems in Minas Gerais, Brazil. Agroforestry Systems, 63(1), 75–82. https://doi.org/10.1023/B:AGFO.0000049435.22512.2d

Chekol, H., Warkineh, B., Shimber, T., Mierek-Adamska, A., Dąbrowska, G. B., & Degu, A. (2024). Drought stress responses in arabica coffee genotypes: Physiological and metabolic insights. Plants, 13(6), 828. https://doi.org/10.3390/plants13060828

de Souza, G. A., Baroni, D. F., Bernado, W., Santos, A. R., Barcellos, L. C., Barcelos, L. F., Correia, L. Z., de Almeida, C. M., Verdin Filho, A. C., Rodrigues, W. P., Ramalho, J. C., Rakočević, M., & Campostrini, E. (2025). Leaf to root morphological and anatomical indicators of drought resistance in Coffea canephora after two stress cycles. Agriculture, 15(6), 574. https://tinyurl.com/2aa7rrnh

dos Santos, C. S., de Freitas, A. F., da Silva, G. H., Pennacchi, J. P., Figueiredo de Carvalho, M. A., Santos, M., Junqueira de Moraes, T. S., de Rezende Abrahão, J. C., Pereira, A. A., Carvalho, G. R., Botelho, C. E., & Silva, V. A. (2023). Phenotypic plasticity index as a strategy for selecting water-stress-adapted coffee genotypes. Plants, 12(23), 4029. https://doi.org/10.3390/plants12234029

Farooq, M., Wahid, A., Kobayashi, N., Fujita, D., & Basra, S. M. A. (2009). Plant drought stress: Effects, mechanisms and management. Agronomy for Sustainable Development, 29(1), 185–212. https://doi.org/10.1051/agro:2008021

Gomez, K. A., & Gomez, A. A. (1983). Statistical procedures for agricultural research (2nd ed.). John Wiley and Sons.

Gutierrez, R. (2010). Competing-risks regression. Stata Conference, Boston, July 15–16. StataCorp.

Kramer, P.J. & Boyer, J.S. (1995). Water relations of plants and soils. Academic Press, San Diego.

Larcher, W. (2003). Physiological plant ecology: Ecophysiology and stress physiology of functional groups (4th ed.). Springer-Verlag Berlin Heidelberg

Lawlor, D. W., & Tezara, W. (2009). Causes of decreased photosynthetic rate and metabolic capacity in water-deficient leaf cells: A critical evaluation of mechanisms and integration of processes. Annals of Botany, 103(4), 561–579. https://doi.org/10.1093/aob/mcn244

Lin, B.B. (2007). Agroforestry management as an adaptive strategy against potential microclimate extremes in coffee agriculture. Agricultural and Forest Meteorology, 144(1–2), 85–94. https://doi.org/10.1016/j.agrformet.2006.12.009

Maestri, M., DaMatta, F. M., Regazzi, A. J., & Barros, R. S. (1995). Accumulation of proline and quaternary ammonium compounds in mature leaves of water-stressed coffee plants (Coffea arabica and C. canephora). Journal of Horticultural Science, 70, 229–233.

Meinzer, F. C., Saliendra, N. Z., & Crisosto, C. H. (1992). Carbon isotope discrimination and gas exchange in Coffea arabica during adjustment to different soil moisture regimes. Australian Journal of Plant Physiology, 19(2), 171–184.

O’Geen, A. T. (2013). Soil water dynamics. Nature Education Knowledge. https://tinyurl.com/y27czzp2

Poorter, H., Bühler, J., van Dusschoten, D., Climent, J., & Postma, J. A. (2012). Pot size matters: A meta-analysis of the effects of rooting volume on plant growth. Functional Plant Biology, 39(11), 839–850. https://doi.org/10.1071/FP12049

Pugnaire, F. I., Serrano, L., & Pardos, J. (1999). Constraints by water stress on plant growth. In M. Pessarakli (Ed.), Handbook of plant and crop stress (pp. 271–283). Marcel Dekker.

Ramirez-Builes, V. H., Küsters, J., Thiele, E., & Lopez-Ruiz, J. C. (2024). Physiological and agronomical response of coffee to different nitrogen forms with and without water stress. Plants, 13(10), 1387. https://doi.org/10.3390/plants13101387

Rosario, D. A., Ocampo, E. M., Sumague, A. C., & Paje, M. C. M. (1992). Adaptation of vegetable legumes to drought stress. In C. G. Kuo (Ed.), Adaptation of food crops to temperature and water stress: Proceedings of an international symposium (pp. 360–371). Asian Vegetable Research and Development Center (AVRDC).

Roonprapant, P., Arunyanark, A., & Chutteang, C. (2021). Morphological and physiological responses to water deficit stress conditions of robusta coffee (Coffea canephora) genotypes in Thailand. Agriculture and Natural Resources, 55(3). https://doi.org/10.34044/j.anres.2021.55.3.18

Sadak, M. S., Tawfik, M. M., & Bakhoum, G. S. (2021). Role of chitosan and chitosan-based nanoparticles on drought tolerance in plants: Probabilities and prospects. In Role of chitosan and chitosan-based nanomaterials in plant sciences (pp. 475–501). Elsevier. https://doi.org/10.1016/B978-0-323-85391-0.00013-7

Satake, A., Sakurai, G., & Kinoshita, T. (2015). Modeling strategies for plant survival, growth, and reproduction. Plant and Cell Physiology, 56(4), 583–585. https://doi.org/10.1093/pcp/pcv041

Silva, P. E. M., Cavatte, P. C., Morais, L. E., Medina, E. F., & DaMatta, F. M. (2013). The functional divergence of biomass partitioning, carbon gain, and water use in Coffea canephora in response to the water supply: Implications for breeding aimed at improving drought tolerance. Environmental and Experimental Botany, 87, 49–57.

Tesfaye, S. G., Ismail, M. R., Kausar, H., Marziah, M., & Ramlan, M. F. (2013). Plant water relations, crop yield, and quality in coffee (Coffea arabica L.) as influenced by partial root zone drying and deficit irrigation. Australian Journal of Crop Science, 7(9), 1361–1368.

Ullah, I., Mao, H., Rasool, G., Gao, H., Javed, Q., Sarwar, A., & Khan, M. I. (2021). Effect of deficit irrigation and reduced fertilization on plant growth, root morphology, and water use efficiency of tomato grown in soilless culture. Agronomy, 11(2), 228. https://doi.org/10.3390/agronomy11020228

Vaast, P., Bertrand, B., Perriot, J., Guyot, B., & Génard, M. (2006). Fruit thinning and shade improve bean characteristics and beverage quality of coffee (Coffea arabica L.) under optimal conditions. Journal of the Science of Food and Agriculture, 86(2), 197–204. https://doi.org/10.1002/jsfa.2338

Verslues, P. E., & Juenger, T. E. (2011). Drought, metabolites, and Arabidopsis natural variation: A promising combination for understanding adaptation to water-limited environments. Current Opinion in Plant Biology, 14(3), 240–245. https://doi.org/10.1016/j.pbi.2011.04.006

Vu, N. T., Park, J. M., Tran, A. T., Bui, T. K., Vu, D. C., & Jang, D. C. (2018). Effect of water stress on the growth and physiology of coffee plants. Journal of Agricultural Life and Environmental Sciences, 2018, 121–130.

Worku, M., & Astatkie, T. (2010). Growth responses of arabica coffee (Coffea arabica L.) varieties to soil moisture deficit at the seedling stage at Jimma, Southwest Ethiopia. Journal of Food, Agriculture and Environment, 8(1), 195–200.

Yang, S., Lan, S., & Gong, M. (2009). Hydrogen peroxide-induced proline and metabolic pathway of its accumulation in maize seedlings. Journal of Plant Physiology, 166(15), 1694–1699. https://doi.org/10.1016/j.jplph.2009.04.006

Zhou, R., Yu, X., Ottosen, C.-O., Rosenqvist, E., Zhao, L., Wang, Y., Yu, W., Zhao, T., & Wu, Z. (2017). Drought stress had a predominant effect overheat stress on three tomato cultivars subjected to combined stress. BMC Plant Biology, 17, 24. https://doi.org/10.1186/s12870-017-0974-x

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Published

2025-06-16

How to Cite

Evasco, R., & Marcelino, J. (2025). Water Deficit Irrigation of Robusta Coffee Under Nursery Conditions in Sultan Kudarat, Philippines. Journal of Interdisciplinary Perspectives, 3(7), 297–313. https://doi.org/10.69569/jip.2025.277