Bund Refugia Alter Arthropod Functional Guild Structure in Lowland Rice (Oryza sativa L.): Evidence from Diversity, Evenness and Dominance Indices
Keywords:
conservation biological control, Cyrtorhinus lividipennis, ecological engineering, parasitoid guild, Sesamum indicum, Vigna radiataAbstract
Vegetation retained on earthen bunds of irrigated rice fields supplies shelter, pollen, nectar and alternative hosts, yet consequences for the arthropod community inside the crop remain unevenly documented. A randomised complete block design with three bund treatments and three replicates was used to quantify arthropod assemblages in transplanted lowland rice across nine weekly samplings (14–70 days after transplanting; DAT). Treatments were cleared bunds (T₀), bunds under spontaneous vegetation (Portulaca oleracea, Cyperus iria, Cyperus rotundus, Eleusine indica; T₁), and bunds sown with sesame (Sesamum indicum) and mungbean (Vigna radiata; T₂). Twenty-seven arthropod taxa in 20 families and 7 orders were recorded (232 individuals). Herbivore relative abundance declined from 11.90% (T₀) to 6.85% (T₁) and 5.33% (T₂), while parasitoid relative abundance rose from 14.29% to 20.55% and 30.67%, lifting the natural-enemy-to-herbivore ratio from 6.00 to 10.40 and 12.75. Shannon diversity peaked at the sixth sampling and fell to zero from 63 DAT onward; seasonal means were 0.93, 0.99 and 1.13. Because indices were computed from pooled catch, the analysis of variance is descriptive: sampling occasion dominated variability whereas bund vegetation explained little (partial η² = 0.09–0.20), with treatment confidence intervals overlapping for every index. Evenness and Simpson dominance remained low across all treatments. A composite decision-support heuristic ranked T₂ first (100.0), ahead of T₁ (49.9) and T₀ (2.3), identifying sesame–mungbean bund refugia as the most promising option for further testing.
References
Alford, L., Roudine, S., Valsami, D., Fontaine-Guenel, T., Namintraporn, T., Guedon, A., Normand, R., Lagneau, L., Le Lann, C., & Van Baaren, J. (2024). No evidence for competition over floral resources between winter-active parasitoids and pollinators in agroecosystems. Scientific Reports, 14, 2239. https://doi.org/10.1038/s41598-024-52146-9
Ali, M. P., Clemente-Orta, G., Kabir, M. M. M., Haque, S. S., Biswas, M., & Landis, D. A. (2023). Landscape structure influences natural pest suppression in a rice agroecosystem. Scientific Reports, 13, 15726. https://doi.org/10.1038/s41598-023-41786-y
Ali, M. P., Rahman, M. S., Nowrin, F., Haque, S. S., Qin, X., Haque, M. A., Uddin, M. M., Landis, D. A., & Howlader, M. T. H. (2021). Salinity influences plant–pest–predator tritrophic interactions. Journal of Economic Entomology, 114(4), 1470–1479. https://doi.org/10.1093/jee/toab133
Babendreier, D., Tang, R., & Horgan, F. G. (2022). Prospects for integrating augmentative and conservation biological control of leaffolders and stemborers in rice. Agronomy, 12(12), 2958. https://doi.org/10.3390/agronomy12122958
Basana Gowda, G., Guru Pirasanna Pandi, G., Ullah, F., Patil, N. B., Sahu, M., Adak, T., Pokhare, S., Yadav, M. K., Mahendiran, A., Mittapelly, P., Desneux, N., & Rath, P. C. (2021). Performance of Trichogramma japonicum under field conditions as a function of the factitious host species used for mass rearing. PLOS ONE, 16(8), e0256246. https://doi.org/10.1371/journal.pone.0256246
Castillo, J., Roda, A., Qureshi, J., Pérez-Hedo, M., Urbaneja, A., & Stansly, P. (2022). Sesame as an alternative host plant to establish and retain predatory mirids in open-field tomatoes. Plants, 11(20), 2779. https://doi.org/10.3390/plants11202779
Chong, H., Zhu, Y., Lai, Q., Wu, S., Jiang, T., Zhang, D., & Xiao, H. (2023). Response of spider and epigaeic beetle assemblages to overwinter planting regimes and surrounding landscape compositions. Insects, 14(12), 951. https://doi.org/10.3390/insects14120951
Colazza, S., Peri, E., & Cusumano, A. (2023). Chemical ecology of floral resources in conservation biological control. Annual Review of Entomology, 68, 13–29. https://doi.org/10.1146/annurev-ento-120220-124357
Cusumano, A., Bella, P., Peri, E., Rostás, M., Guarino, S., Lievens, B., & Colazza, S. (2023). Nectar-inhabiting bacteria affect olfactory responses of an insect parasitoid by altering nectar odors. Microbial Ecology, 86(1), 364–376. https://doi.org/10.1007/s00248-022-02078-6
Gurr, G. M., Liu, J., & Pogrebna, G. (2024). Harnessing artificial intelligence for analysing the impacts of nectar and pollen feeding in conservation biological control. Current Opinion in Insect Science, 62, 101176. https://doi.org/10.1016/j.cois.2024.101176
Herz, A., Dingeldey, E., & Englert, C. (2021). More power with flower for the pupal parasitoid Trichopria drosophilae: A candidate for biological control of the spotted wing drosophila. Insects, 12(7), 628. https://doi.org/10.3390/insects12070628
Horgan, F. G., Vu, Q., Mundaca, E. A., & Crisol-Martínez, E. (2022). Restoration of rice ecosystem services: “Ecological engineering for pest management” incentives and practices in the Mekong Delta region of Vietnam. Agronomy, 12(5), 1042. https://doi.org/10.3390/agronomy12051042
Hyder, M., Li, Y., Raza, M. F., Zhang, M., Chen, J., Mao, J., Bukero, A., & Zhang, L. (2023). Enhancing Coccinella beetle biological pest control via a floral approach in cucumber greenhouse. Life, 13(10), 2080. https://doi.org/10.3390/life13102080
Khetnon, P., Busarakam, K., Sukhaket, W., Niwaspragrit, C., Kamolsukyeunyong, W., Kamata, N., & Sanguansub, S. (2022). Mechanisms of trichomes and terpene compounds in indigenous and commercial Thai rice varieties against brown planthopper. Insects, 13(5), 427. https://doi.org/10.3390/insects13050427
Klinnert, A., Barbosa, A. L., Catarino, R., Fellmann, T., Baldoni, E., Beber, C., Hristov, J., Paracchini, M. L., Rega, C., Weiss, F., Witzke, P., & Rodriguez-Cerezo, E. (2024). Landscape features support natural pest control and farm income when pesticide application is reduced. Nature Communications, 15, 5384. https://doi.org/10.1038/s41467-024-48311-3
Layek, U., Bhandari, T., Das, A., & Karmakar, P. (2024). Floral visitors of sesame (Sesamum indicum L.): Elucidating their nectar-robbing behaviour and impacts on the plant reproduction. PLOS ONE, 19(4), e0300398. https://doi.org/10.1371/journal.pone.0300398
Liu, Q., Hu, X., Su, S., Ning, Y., Peng, Y., Ye, G., Lou, Y., Turlings, T. C. J., & Li, Y. (2021). Cooperative herbivory between two important pests of rice. Nature Communications, 12, 6772. https://doi.org/10.1038/s41467-021-27021-0
Peñalver-Cruz, A., & Horgan, F. G. (2022). Interactions between rice resistance to planthoppers and honeydew-related egg parasitism under varying levels of nitrogenous fertilizer. Insects, 13(3), 251. https://doi.org/10.3390/insects13030251
Qian, P., Bai, Y., Zhou, W., Yu, H., Zhu, Z., Wang, G., Quais, M. K., Li, F., Chen, Y., Tan, Y., Shi, X., Wang, X., Zhong, X., & Zhu, Z.-R. (2021). Diversified bund vegetation coupled with flowering plants enhances predator population and early-season pest control. Environmental Entomology, 50(4), 842–851. https://doi.org/10.1093/ee/nvab027
Ray, A., Gadratagi, B. G., Budhlakoti, N., Rana, D. K., Adak, T., Govindharaj, G. P. P., Patil, N. B., Mahendiran, A., & Rath, P. C. (2023). Functional response of an egg parasitoid, Trichogramma chilonis Ishii, to sublethal imidacloprid exposure. Pest Management Science, 79(10), 3656–3665. https://doi.org/10.1002/ps.7540
Rosida, N., Ibrahim, E., Senoaji, W., Sidik, E. A., Mugiasih, A., Khaerana, Hutasoit, R. T., Firmansyah, Praptana, R. H., Sudewi, S., & Nasruddin, A. (2025). Harnessing flowering bund plants through ecological engineering to improve biological control of tungro virus vectors in rice field agroecosystems. International Journal of Food Science, 2025, 2476370. https://doi.org/10.1155/ijfo/2476370
Seimandi-Corda, G., MacLaren, C., Tougeron, K., Forkman, J., Hood, J., Mead, A., Dixon, A., & Cook, S. M. (2026). Implementation of practices shapes the effectiveness of agricultural diversification for arthropod related ecosystem services: A meta-analysis. Agronomy for Sustainable Development, 46(2), 19. https://doi.org/10.1007/s13593-025-01082-7
Sun, J., Song, X., He, J., Chen, D., Yang, T., & Shi, A. (2025). Rice stubble provides overwintering microhabitats for spiders in winter-fallowed rice fields. Agriculture, 15(4), 381. https://doi.org/10.3390/agriculture15040381
Sun, Z., Shi, J. H., Liu, H., Yin, L. T., Abdelnabby, H., & Wang, M. Q. (2021). Phytopathogenic infection alters rice–pest–parasitoid tri-trophic interactions. Pest Management Science, 77(10), 4530–4538. https://doi.org/10.1002/ps.6491
Tian, Z., Wang, Y., Sun, T., Hu, X., Hao, W., Zhao, T., Wang, Y., Zhang, L., Jiang, X., Turlings, T. C. J., & Li, Y. (2025). An egg parasitoid assesses host egg quality from afar using oviposition-induced plant volatiles. Current Biology, 35(13), 3001–3010. https://doi.org/10.1016/j.cub.2025.04.066
Vu, Q., Dossa, G. S., Mundaca, E. A., Settele, J., Crisol-Martínez, E., & Horgan, F. G. (2022). Combined effects of soil silicon and host plant resistance on planthoppers, blast and bacterial blight in tropical rice. Insects, 13(7), 604. https://doi.org/10.3390/insects13070604
Wang, L., Wu, H., He, W., Lai, G., Li, J., Liu, S., & Zhou, Q. (2024). Diversity of parasitoid wasps and comparison of sampling strategies in rice fields using metabarcoding. Insects, 15(4), 228. https://doi.org/10.3390/insects15040228
Yao, C., Du, L., Liu, Q., Hu, X., Ye, W., Turlings, T. C. J., & Li, Y. (2022). Stemborer-induced rice plant volatiles boost direct and indirect resistance in neighboring plants. New Phytologist, 237(6), 2375–2387. https://doi.org/10.1111/nph.18548
Yele, Y., Chander, S., Suroshe, S. S., Nebapure, S., Tenguri, P., & Pattathanam Sundaran, A. (2023). Ecological engineering in low land rice for brown plant hopper, Nilaparvata lugens (Stål) management. PeerJ, 11, e15531. https://doi.org/10.7717/peerj.15531
Zhong, Y., Liao, X., & Hou, M. (2023). Predatory capacity and reproduction of Cyrtorhinus lividipennis (Hemiptera: Miridae) adults exposed to low-temperature storage and fitness of the F1 generation. Insects, 14(3), 226. https://doi.org/10.3390/insects14030226
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