Rambutan Seedling Morphology Under Intact and Divided Seed Treatments With Putative Polyembryony

Authors

  • Ir. STANLEY ADRIAN F. WALINGKAS, M.P Department of Agronomy, Faculty of Agriculture, Universitas Sam Ratulangi, Manado 95115, Indonesia
  • PEMMY TUMEWU M.P Department of Agronomy, Faculty of Agriculture, Universitas Sam Ratulangi, Manado 95115, Indonesia
  • Frangky Jessy Paat Department of Agrotechnology , Faculty of Agriculture, Universitas Sam Ratulangi, Manado 95115, Indonesia

DOI:

https://doi.org/10.35791/jat.v7i4.70710

Keywords:

nursery management, polyembryony, rambutan, root dry mass, seedling morphology

Abstract

Rambutan (Nephelium lappaceum L.) propagation requires nursery planting material with adequate vegetative growth. Multiple emergence from a single seed and longitudinal seed division may influence the morphology of seedlings available for transplantation, although multiple emergence alone does not establish polyembryony. This study characterized seedlings associated with intact and divided seeds in five post-emergence groups: Z1 (one seedling from intact seed), PU2 and PU3 (two and three seedlings from intact seed), and PB2 and PB3 (two and three seedlings associated with divided seed). A four-block nursery arrangement was used, with three seeds initially planted per plot. Leaf number, seedling height, stem diameter, leaf area, and root dry mass were assessed in surviving seedlings at 12 weeks after planting. Z1 showed the highest mean leaf number (6.08), height (31.68 cm), diameter (0.395 cm), leaf area (174.07 cm²), and root dry mass (1.88 g). Within the two-seedling class, PU2 and PB2 had similar height means (26.36 and 26.86 cm), whereas PU3 and PB3 differed more clearly in leaf area (111.28 and 135.09 cm²). The results document trait-specific morphological variation but do not establish causal treatment superiority or embryological origin. Multitrait seedling assessment can support nursery selection, while propagation efficiency must be evaluated separately from individual seedling size.

References

Andrade, R. A. de, Bagatim, A. G., & Nacata, G. (2018). Rambutan seed germination: Temperature and storage. Comunicata Scientiae, 8(2), 383–388. https://doi.org/10.14295/cs.v8i2.2114

Cavalcante, Í. H. L., Segeren, A., & Martins, A. B. G. (2008). Emergence and initial growth of rambutan seedlings as a function of seed storage conditions. Fruits, 63(6), 349–355. https://doi.org/10.1051/fruits:2008031

Chandra, J., Dubey, M., Varghese, B., Sershen, & Keshavkant, S. (2021). Towards understanding the basis of desiccation-induced oxidative stress in recalcitrant seeds: The case of Madhuca latifolia Roxb. South African Journal of Botany, 142, 100–105. https://doi.org/10.1016/j.sajb.2021.06.012

Che Lah, N. H., El Enshasy, H. A., Mediani, A., Azizan, K. A., Aizat, W. M., Tan, J. K., Afzan, A., Mohd Noor, N., & Rohani, E. R. (2023). An insight into the behaviour of recalcitrant seeds by understanding their molecular changes upon desiccation and low temperature. Agronomy, 13(8), 2099. https://doi.org/10.3390/agronomy13082099

Cruz-Arvizu, O., Villegas-Monter, A., Alarcón-Zúñiga, B., Gutiérrez-Espinosa, M. A., & González-Hernández, V. A. (2025). Beyond zygotic and nucellar origins: Improving the polyembryony model in citrus. Planta, 263, 18. https://doi.org/10.1007/s00425-025-04876-x

Finch-Savage, W. E., & Bassel, G. W. (2016). Seed vigour and crop establishment: Extending performance beyond adaptation. Journal of Experimental Botany, 67(3), 567–591. https://doi.org/10.1093/jxb/erv490

Jia, H.-H., Xu, Y.-T., Yin, Z.-P., Wu, X.-M., Qing, M., Fan, Y.-J., Song, X., Xie, K.-D., Xie, Z.-Z., Xu, Q., Deng, X.-X., & Guo, W.-W. (2021). Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus. DNA Research, 28(5), dsab014. https://doi.org/10.1093/dnares/dsab014

Kijak, H., & Ratajczak, E. (2020). What do we know about the genetic basis of seed desiccation tolerance and longevity? International Journal of Molecular Sciences, 21(10), 3612. https://doi.org/10.3390/ijms21103612

Martínez-Ochoa, E. del C., Villegas-Velázquez, I., Alarcón-Zúñiga, B., González-Hernández, V. A., & Villegas-Monter, A. (2022). Polyembryony in citrus: Does the largest embryo in the seed develop a nucellar seedling? Scientia Agricola, 79(6), e20200060. https://doi.org/10.1590/1678-992X-2020-0060

Oliver, M. J., Farrant, J. M., Hilhorst, H. W. M., Mundree, S., Williams, B., & Bewley, J. D. (2020). Desiccation tolerance: Avoiding cellular damage during drying and rehydration. Annual Review of Plant Biology, 71, 435–460. https://doi.org/10.1146/annurev-arplant-071219-105542

Reed, R. C., Bradford, K. J., & Khanday, I. (2022). Seed germination and vigor: Ensuring crop sustainability in a changing climate. Heredity, 128, 450–459. https://doi.org/10.1038/s41437-022-00497-2

Tetteh, R., Aboagye, L. M., Osafo, E. A., Darko, R., Dassah, A., & Obirih-Opareh, J. (2022). Effect of tree age on fruit characteristics, seed emergence and seedling growth in rambutan (Nephelium lappaceum L.). Journal of Horticultural Sciences, 17(1), 245–248. https://doi.org/10.24154/jhs.v17i1.991

Tetteh, R., Nketiah, V., Obirih-Opareh, J., Ibrahim, A.-A., & Kotey, D. A. (2023). Exploring the growth and development of rambutan (Nephelium lappaceum L.) seedlings: The impact of fruit maturation on seed germination, seedling growth and biomass partitioning. Bhartiya Krishi Anusandhan Patrika, 38(3), 296–300. https://doi.org/10.18805/BKAP632

Underwood, C. J., & Mercier, R. (2022). Engineering apomixis: Clonal seeds approaching the fields. Annual Review of Plant Biology, 73, 201–225. https://doi.org/10.1146/annurev-arplant-102720-013958

Wang, N., Song, X., Ye, J., Zhang, S., Cao, Z., Zhu, C., Hu, J., Zhou, Y., Huang, Y., Cao, S., Liu, Z., Wu, X., Chai, L., Guo, W., Xu, Q., Gaut, B. S., Koltunow, A. M. G., Zhou, Y., & Deng, X. (2022). Structural variation and parallel evolution of apomixis in citrus during domestication and diversification. National Science Review, 9(10), nwac114. https://doi.org/10.1093/nsr/nwac114

Woo, J.-K., Park, Y. C., Lee, J. W., Yun, S.-H., Kim, M., Park, S., Lee, Y., Song, K. J., & Kim, H. B. (2019). Evaluation of polyembryony for genetic resources and efficacy of simple sequence repeat markers for the identification of nucellar and zygotic embryo-derived individuals in citrus. Applied Biological Chemistry, 62, 30. https://doi.org/10.1186/s13765-019-0437-1

Xu, Y., Jia, H., Wu, X., Koltunow, A. M. G., Deng, X., & Xu, Q. (2021). Regulation of nucellar embryony, a mode of sporophytic apomixis in Citrus resembling somatic embryogenesis. Current Opinion in Plant Biology, 59, 101984. https://doi.org/10.1016/j.pbi.2020.101984

Xu, Y., Jia, H., Tan, C., Wu, X., Deng, X., & Xu, Q. (2022). Apomixis: Genetic basis and controlling genes. Horticulture Research, 9, uhac150. https://doi.org/10.1093/hr/uhac150

Yin, P., Tang, L., Zhang, X., & Su, Y. (2022). Options for engineering apomixis in plants. Frontiers in Plant Science, 13, 864987. https://doi.org/10.3389/fpls.2022.864987

Downloads

Published

2026-11-11

How to Cite

Rambutan Seedling Morphology Under Intact and Divided Seed Treatments With Putative Polyembryony. (2026). Jurnal Agroekoteknologi Terapan, 7(4), 983-991. https://doi.org/10.35791/jat.v7i4.70710