<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "https://jats.nlm.nih.gov/publishing/1.3/JATS-journalpublishing1-3.dtd"><article xml:lang="en" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" dtd-version="1.3" article-type="research-article"><front><journal-meta><journal-id journal-id-type="issn">2089-0257</journal-id><journal-title-group><journal-title>Jurnal Entomologi Indonesia</journal-title><abbrev-journal-title>J Entomol Indones</abbrev-journal-title></journal-title-group><issn pub-type="epub">2089-0257</issn><issn pub-type="ppub">1829-7722</issn><publisher><publisher-name>Perhimpunan Entomologi Indonesia</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.5994/jei.23.2.1</article-id><article-categories></article-categories><title-group><article-title>Predatory behavior and predation efficiency of Sycanus sp. against Metisa plana Walker: Implications for biological control in oil palm</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ikhsan</surname><given-names>Zahlul</given-names></name><address><country country="ID">Indonesia</country><email>zahlulikhsan@agr.unand.ac.id</email></address><xref ref-type="aff" rid="AFF-1"></xref><xref ref-type="corresp" rid="cor-0"></xref></contrib><contrib contrib-type="author"><name><surname>Aisyah</surname><given-names>Mona</given-names></name><address><country country="ID">Indonesia</country><email>monaaisyah@gmail.com</email></address><xref ref-type="aff" rid="AFF-1"></xref></contrib><contrib contrib-type="author"><name><surname>Rozen</surname><given-names>Nalwida</given-names></name><address><country country="ID">Indonesia</country><email>nalwidarozen@agr.unand.ac.id</email></address><xref ref-type="aff" rid="AFF-2"></xref></contrib><contrib contrib-type="author"><name><surname>Heriza</surname><given-names>Sri</given-names></name><address><country country="ID">Indonesia</country><email>sriheriza@agr.unand.ac.id</email></address><xref ref-type="aff" rid="AFF-1"></xref></contrib><contrib contrib-type="author"><name><surname>Bakry</surname><given-names>Moustafa Sabry</given-names></name><address><country country="EG">Egypt</country><email>md.md_sabry@yahoo.com</email></address><xref ref-type="aff" rid="AFF-3"></xref></contrib><contrib contrib-type="author"><name><surname>Maulana</surname><given-names>Amsar</given-names></name><address><country country="ID">Indonesia</country><email>amaulanapurnomo.1005@gmail.com</email></address><xref ref-type="aff" rid="AFF-4"></xref></contrib><contrib contrib-type="author"><name><surname>Zainudin</surname><given-names>Nur Ain Izzati Mohd</given-names></name><address><country country="MY">Malaysia</country><email>ainizzati@upm.edu.my</email></address><xref ref-type="aff" rid="AFF-5"></xref></contrib></contrib-group><contrib-group><contrib contrib-type="editor"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4389-0261</contrib-id><name><surname>Nurindah</surname><given-names>Nurindah</given-names></name><address><country country="ID">Indonesia</country><email>nurindah@brin.go.id</email></address></contrib></contrib-group><aff id="AFF-1"><institution content-type="dept">Department of Agroecotechnology, Faculty of Agriculture</institution><institution-wrap><institution>Andalas University</institution><institution-id institution-id-type="ror">https://ror.org/04ded0672</institution-id></institution-wrap><addr-line>Dharmasraya, West Sumatra 27573</addr-line><country country="ID">Indonesia</country></aff><aff id="AFF-2"><institution content-type="dept">Department of Agrotechnology, Faculty of Agriculture</institution><institution-wrap><institution>Andalas University</institution><institution-id institution-id-type="ror">https://ror.org/04ded0672</institution-id></institution-wrap><addr-line>Limau Manis, Padang, West Sumatra 25163</addr-line><country country="ID">Indonesia</country></aff><aff id="AFF-3"><institution content-type="dept">Plant Protection Research Institute</institution><institution-wrap><institution>Agricultural Research Center</institution><institution-id institution-id-type="ror">https://ror.org/027m8zy97</institution-id></institution-wrap><addr-line>Nadi El-Said Street-Dokki, Giza 3751254</addr-line><country country="AZ">Azerbaijan</country></aff><aff id="AFF-4"><institution-wrap><institution>Food Safety Authority of Ireland</institution><institution-id institution-id-type="ror">https://ror.org/00bm89f36</institution-id></institution-wrap><addr-line>Research Center for Food Technology and Processing, National Research and Innovation Agency (BRIN), Jogja-Wonosari Km. 31.5 Street, Yogyakarta 55861</addr-line><country country="IE">Ireland</country></aff><aff id="AFF-5"><institution content-type="dept">Department of Biology, Faculty of Science</institution><institution-wrap><institution>Universiti Putra Malaysia</institution><institution-id institution-id-type="ror">https://ror.org/02e91jd64</institution-id></institution-wrap><addr-line>Serdang, Selangor, 43400</addr-line><country country="MY">Malaysia</country></aff><author-notes><corresp id="cor-0">Corresponding author: Zahlul Ikhsan. Email: <email>zahlulikhsan@agr.unand.ac.id</email></corresp></author-notes><pub-date date-type="pub" iso-8601-date="2026-07-31" publication-format="electronic"><day>31</day><month>07</month><year>2026</year></pub-date><pub-date date-type="collection" iso-8601-date="2026-07-31" publication-format="electronic"><day>31</day><month>07</month><year>2026</year></pub-date><volume>23</volume><issue>2</issue><issue-title>July</issue-title><fpage>91</fpage><lpage>98</lpage><history><date date-type="received" iso-8601-date="2026-02-19"><day>19</day><month>02</month><year>2026</year></date><date date-type="accepted" iso-8601-date="2026-06-22"><day>22</day><month>06</month><year>2026</year></date></history><permissions><copyright-statement>Copyright (c) 2026 Zahlul Ikhsan, Mona Aisyah, Nalwida Rozen, Sri Heriza, Moustafa Sabry Bakry, Amsar Maulana, Nur Ain Izzati Mohd Zainudin</copyright-statement><copyright-year>2026</copyright-year><copyright-holder>Zahlul Ikhsan, Mona Aisyah, Nalwida Rozen, Sri Heriza, Moustafa Sabry Bakry, Amsar Maulana, Nur Ain Izzati Mohd Zainudin</copyright-holder><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0/</ali:license_ref><license-p>This work is licensed under a Creative Commons Attribution 4.0 International License.Authors who publish with this journal agree to the following terms:Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution 4.0 International License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).</license-p></license></permissions><self-uri xlink:href="https://jurnal.pei-pusat.org/index.php/jei/article/view/995" xlink:title="995"></self-uri><abstract><p>Bagworm (Metisa plana Walker) is a major defoliating pest of oil palm, causing significant yield losses during outbreaks. Biological control using predatory insects offers an environmentally sustainable alternative to chemical insecticides. This study evaluated the predatory performance of Sycanus sp. against M. plana larvae and assessed the effect of predator density on prey suppression under laboratory conditions. A completely randomized design was used with five predator-density treatments (1, 2, 3, 4, and 5 predators per 10 larvae) and ten replications. Predator performance was evaluated based on prey-search duration, handling time, larval mortality, and prey consumption. The initial prey-search duration ranged from 2.11 to 2.25 min, while subsequent searches ranged from 1.69 to 2.04 min. Prey-handling time remained relatively constant across treatments (58.1-59.1 min). Predation by Sycanus sp. substantially reduced M. plana populations within three days, with the highest mortality occurring on the first day after predator introduction. Predator density significantly increased prey consumption, which rose from 1.26 ± 0.21 larvae at one predator to 4.43 ± 0.19 larvae at five predators. A strong positive relationship was observed between predator density and prey consumption (y = 0.795x + 0.451; R² = 0.9531). Although the highest prey suppression occurred at the greatest predator density, a ratio of two Sycanus sp. adults per ten M. plana larvae provided a favorable balance between prey suppression and predator deployment efficiency. These findings support the potential use of Sycanus sp. as a biological control agent in sustainable oil palm integrated pest management programs.</p></abstract><kwd-group><kwd>bagworm management</kwd><kwd>biological control</kwd><kwd>oil palm</kwd><kwd>predator-prey dynamics</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>File created by JATS Editor</meta-name><meta-value>https://jatseditor.com</meta-value></custom-meta><custom-meta><meta-name>issue-created-year</meta-name><meta-value>2026</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="sec-1"><title>INTRODUCTION</title><p>The oil palm (Elaeis guineensis Jacq.) has emerged as a pivotal crop in Indonesia, representing a significant investment in the agricultural sector and economic development. Indonesia cultivates more than 16 million ha of oil palm, making it the world’s largest producer <xref ref-type="bibr" rid="BIBR-5">(Statistik, 2026)</xref>. The expansion of oil palm plantations has been accompanied by a remarkable increase in production, with figures rising from 21.14 million tons in 2022 to an anticipated 23.28 million tons in 2023. This growth underscores the importance of effective agricultural practices, particularly pest management, to sustain and enhance productivity.</p><p>Pest management in oil palm cultivation is critical, as various pests can significantly hinder plant growth and reduce yields. Among these pests, the bagworm, Metisa plana Walker (Lepidoptera: Psychidae) has been identified as particularly damaging, capable of causing substantial economic losses in oil palm plantations (<xref ref-type="bibr" rid="BIBR-21">Sigalingging et al. 2025</xref>; <xref ref-type="bibr" rid="BIBR-25">Thaer et al. 2021</xref>). The impact of pests such as the oil palm leaf-eating caterpillar and other members of the Coleoptera and Lepidoptera orders has been well documented, with studies indicating that these organisms can cause production losses of 40% to 60%. The urgency of addressing pestrelated challenges in oil palm cultivation is further underscored by M. plana’s adaptive capabilities, which enable it to proliferate rapidly and spread quickly through both physical contact and wind (<xref ref-type="bibr" rid="BIBR-12">Ikhsan et al. 2024</xref>; <xref ref-type="bibr" rid="BIBR-7">Egonyu et al. 2022</xref>).</p><p>Although M. plana is known to damage oil palm plantations, there are gaps in the literature regarding its management. Current control measures, such as removal or pesticide use, have been ineffective and are likely to worsen the impact on environmental health and lead to pest resistance. Reliance on chemical control is likely to disrupt the ecological balance and is a major concern for the sustainability of farm systems <xref ref-type="bibr" rid="BIBR-19">(Priyanka et al. 2024)</xref>. For that reason, there is an urgent need to develop new sustainable strategies to manage this pest without compromising ecosystem integrity. Of the many approaches to sustainable pest management, biological control using natural enemies is among the most effective. Sycanus sp. may help control M. plana and other larvae of Lepidoptera, as this predator feeds through a unique method that sucks the hemolymph of its prey (Hendarjanti et al. 2024; <xref ref-type="bibr" rid="BIBR-24">Sucahyono et al. 2022</xref>; <xref ref-type="bibr" rid="BIBR-28">Yuliadhi et al. 2021</xref>).</p><p>Research on Sycanus spp. has focused on predation and prey consumption. Despite numerous studies, predation rates and integrated evaluations that combine prey-search behavior, handling time, temporal mortality dynamics, and density-dependent predation efficiency against M. plana remain lacking. The vast majority of studies have focused on Sycanus dichotomus Stål, where predation searching behavior, predation and prey-handling times, and patterns of predation and mortality have been poorly studied (<xref ref-type="bibr" rid="BIBR-9">Hayati et al. 2024</xref>; <xref ref-type="bibr" rid="BIBR-15">Jamian &amp; Adam 2018</xref>; <xref ref-type="bibr" rid="BIBR-3">Ahmad &amp; Kamaruddin 2016</xref>). Consequently, information remains limited regarding how behavioral processes influence predation efficiency and biological control potential. A more integrated assessment of both behavioral and quantitative predation parameters is therefore needed to improve understanding of predator–prey interactions and to support the development of effective biological control strategies for M. plana in oil palm agroecosystems.</p><p>Moreover, methodological variability in predator source and age structure complicates the interpretation of predation capacity. Field-collected predators can present substantial heterogeneity in age, physiological condition, prior feeding history, and reproductive status, potentially confounding estimates of predatory performance. Laboratoryreared, generation-standardized predators, such as first-generation (F1) females, offer a more rigorous framework for assessing intrinsic predatory traits and behavioral characteristics, enabling clearer inferences about predator efficacy in biological control programs (<xref ref-type="bibr" rid="BIBR-1">Adhikary et al. 2025</xref>; <xref ref-type="bibr" rid="BIBR-17">Melketa et al. 2022</xref>; <xref ref-type="bibr" rid="BIBR-15">Jamian &amp; Adam 2018</xref>).</p><p>To our knowledge, no previous study has simultaneously evaluated prey-search behavior, prey-handling time, mortality dynamics, and densitydependent predatory performance in laboratoryreared F1 female Sycanus spp. targeting M. plana. Understanding these elements of predatory dynamics is necessary to assess the effectiveness of predation and is crucial for developing ecologically based pest management strategies for oil palm agroecosystems.</p><p>This study provides an integrated evaluation of prey-search behavior, prey-handling time, temporal mortality dynamics, and density-dependent predation of laboratory-reared F1 female Sycanus sp. against M. plana. By combining behavioral and quantitative measures of predation, this study provides a more comprehensive understanding of predator–prey interactions and the potential application of Sycanus sp. in sustainable biological control of bagworms in oil palm ecosystems. Based on ratio-dependent predation theory <xref ref-type="bibr" rid="BIBR-4">(Arditi &amp; Ginzburg 1989)</xref>, we hypothesized that increasing predator density would increase total prey suppression but would reduce per-capita predation efficiency because multiple predators compete for the same prey resources.</p><p>This research aims to investigate Sycanus sp. predation on M. plana and the associated predatory behavior in a controlled laboratory setting. These findings could help to optimize the use of assassin bugs as biological control agents in oil palm plantations and support environmentally friendly integrated pest management.</p></sec><sec id="sec-2"><title>MATERIALS AND METHODS</title><p>The study was conducted between January and September 2024 at the Integrated Pest Management Laboratory, Faculty of Agriculture, Universitas Andalas, West Sumatra, Indonesia.</p><sec id="sec-3"><title>Collection and rearing of Sycanus sp. and M. plana</title><p>Adult Sycanus sp. and M. plana larvae were initially collected from oil palm plantations via direct field sampling, following established procedures (Cuthbert et al. 2021). The founder population of Sycanus sp. was collected from an oil palm plantation in Labuhanbatu Regency, North Sumatra province, Indonesia <inline-formula><tex-math id="math-1"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle ( 2 ^ { \circ } 0 9 ^ { \prime } \mathrm { N } , 9 9 ^ { \circ } 4 3 ^ { \prime } \mathrm { E } ) \end{document} ]]></tex-math></inline-formula> . Adult predators were commonly observed on flowering refugia plants, including Helianthus annuus, Cosmos sulphureus, Turnera subulata, and Calopogonium mucunoides. These plants serve as important habitats for natural enemies. To minimize variability typical of fieldcollected insects, all predators used in the experiment were laboratory-reared F1 Sycanus sp. derived from this parental population and used 15 days after adult emergence. Metisa plana larvae (third-fourth instars) were collected from smallholder oil palm plantations with active infestations. The larvae were carefully removed from the undersides of oil palm leaflets and maintained under laboratory conditions prior to experimentation.</p></sec></sec><sec id="sec-4"><title>Experimental design</title><p>A laboratory experiment was conducted using a completely randomized design (CRD) to evaluate the predatory interaction between Sycanus sp. and M. plana. Oil palm seedlings were used as the host plant and food source for M. plana larvae throughout the experiment. The experiment consisted of five predator-density treatments, each replicated 10 times, for a total of 50 experimental units (each an individual observation arena). All predators were laboratory-reared F1 female Sycanus sp., aged 15 days after adult emergence, standardized to minimize individual variability; only females were used to avoid sex-related behavioral differences and ensure uniform predatory performance. The five treatments comprised 1, 2, 3, 4, and 5 female Sycanus sp. (P1–P5, respectively), each with 10 M. plana larvae. Predators were then introduced into the units containing the assigned number of M. plana larvae, and predation activity and predator–prey interactions were observed.</p></sec><sec id="sec-5"><title>Observation and data analysis</title><p>Behavioral observations were conducted in transparent plastic containers (20 cm × 15 cm × 15 cm) covered with fine mesh to prevent insect escape while allowing ventilation, at <inline-formula><tex-math id="math-2"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle 2 7 \pm 2 ^ { \circ } \mathrm { C } , \end{document} ]]></tex-math></inline-formula><inline-formula><tex-math id="math-3"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle 7 0 \pm 1 0 \% \end{document} ]]></tex-math></inline-formula> relative humidity, and a 12:12 h (L:D) photoperiod. Before each observation, predators were individually isolated and starved for 12 h to standardize hunger and feeding motivation <xref ref-type="bibr" rid="BIBR-15">(Jamian &amp; Adam 2018)</xref>. Each arena then received M. plana larvae according to the assigned treatment.</p><p>Predatory performance of Sycanus sp. against M. plana was evaluated using both qualitative and quantitative observations: (a) prey search time, determined as the interval from predator introduction to the first successful prey encounter; (b) prey handling time, measured as the interval from initial contact until the prey was completely immobilized; (c) prey consumption, the number of larvae consumed during the observation period; (d) larval mortality, assessed at 24-hour intervals after predator introduction using the formula <xref ref-type="bibr" rid="BIBR-8">(Ge et al. 2019)</xref>:</p><disp-formula id="equation-1"><tex-math id="math-4"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle M = \frac{a}{a + b} \times 100, where \end{document} ]]></tex-math></disp-formula><p>M: mortality of larvae (%); a: number of dead larvae; and b: number of larvae treated.</p><p>Data were analyzed in Microsoft Excel 2016 and SPSS version 23. One-way analysis of variance (ANOVA) tested the effects of predator density on prey search duration, prey handling time, larval mortality, and prey consumption. Where treatments differed significantly, means were separated using Duncan’s multiple range test (DMRT) at <inline-formula><tex-math id="math-5"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle P = 0.05. \end{document} ]]></tex-math></inline-formula> Linear regression assessed the relationship between predator density and prey consumption.</p></sec><sec id="sec-6"><title>RESULTS</title><sec id="sec-7"><title>Prey search behavior of Sycanus sp. on M. plana</title><p>The prey-search behavior of Sycanus sp. showed clear temporal patterns throughout the experimental period (<xref ref-type="fig" rid="figure-2">Figure 2</xref>). The first search was consistently longer than later ones: the initial search for 10 M. plana larvae ranged from 2.11 to 2.25 minutes across all predator densities, with no consistent trend as predator density increased. In contrast, subsequent searches were markedly shorter (1.69 to 2.04 minutes) and decreased slightly at higher predator densities. This shortening after the first capture indicates that the predator shifted to a more efficient hunting state, possibly reflecting a higher encounter probability within the confined arena, although the underlying behavioral mechanisms were not directly quantified.</p></sec></sec><sec id="sec-8"><title>Prey handling time of Sycanus sp.</title><p>Total handling time for 10 M. plana varied across predator densities, ranging from 58.1 to 59.1 minutes (Figure 2). These minimal differences, indicate that predator density did not substantially affect the duration of the prey handling process, suggesting that Sycanus sp. requires a relatively constant time to capture, immobilize, and consume prey, regardless of the number of conspecifics present. The mechanism by which Sycanus sp. handles M. plana involves piercing the larval cuticle with its rostrum and extracting internal body fluids by sucking, leading to progressive desiccation and eventual death of the larvae. The death of M. plana was characterized by the larvae exiting their larval sacs, a clear and reliable indicator of successful predation.</p><fig id="figure-1"><label>Figure 1</label><caption><p>Sycanus sp. search time preying on Metisa plana. Different letters indicate significant differences (DMRT, P = 0.05).</p></caption><graphic xlink:href="https://www.jurnal.pei-pusat.org/index.php/jei/article/download/995/673/9636" mime-subtype="jpeg" mimetype="image"><alt-text>Figure 1</alt-text></graphic></fig><fig id="figure-2"><label>Figure 2.</label><caption><p>Handling time of Sycanus sp. from first attack to immobilization of Metisa plana. Different letters indicate significant differences (DMRT, P = 0.05).</p></caption><graphic xlink:href="https://www.jurnal.pei-pusat.org/index.php/jei/article/download/995/673/9637" mime-subtype="jpeg" mimetype="image"><alt-text>Figure 2.</alt-text></graphic></fig></sec><sec id="sec-9"><title>Mortality rates of M. plana due to predation by Sycanus sp.</title><p>Metisa plana mortality was recorded daily for three days predator introduction (days after application, DAA) until few or no larvae remained (<xref ref-type="fig" rid="figure-3">Figure 3</xref>).</p><p>Across all predator-to-prey ratios, mortality was highest on the first day (DAA = 1) and declined thereafter. On DAA = 1, the 5:10, 4:10, 3:10, 2:10, and 1:10 ratios recorded killed 9, 8, 7, 6, and 5 larvae, respectively; mortality then fell sharply to 1–3 larvae on DAA = 2, and by DAA = 3 only 0 to 1 M. plana larvae remained. Most predation therefore occurred soon after Sycanus sp. introduction, with the 5:10 ratio being most effective in achieving early elimination of M. plana.</p><sec id="sec-10"><title>Density-dependent effects on predation efficiency</title><p> Predator density had a strong positive effect on prey consumption. The mean number of larvae consumed rose steadily with density from <inline-formula><tex-math id="math-6"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle 1 . 2 6 \pm 0 . 2 1 \end{document} ]]></tex-math></inline-formula> larvae at one predator to <inline-formula><tex-math id="math-7"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle 2 . 0 5 \pm 0 . 1 8 , 2 . 7 4 \pm 0 . 1 7 , \end{document} ]]></tex-math></inline-formula> , and 3.64 ± 0.20 larvae at two, three, and four predators, and <inline-formula><tex-math id="math-8"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle 4 . 4 3 \pm 0 . 1 9 \end{document} ]]></tex-math></inline-formula> larvae at five predators per 10 larvae (<xref ref-type="fig" rid="figure-4">Figure 4</xref>). Linear regression confirmed a significant positive relationship between predator density and prey consumption, <inline-formula><tex-math id="math-9"><![CDATA[ \documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle y = 0.795x + 0.451; R^{2} = 0.9531 \end{document} ]]></tex-math></inline-formula> indicating that predator density explained about 95% of the variation in prey consumption.</p></sec></sec><sec id="sec-11"><title>DISCUSSION</title></sec><sec id="sec-12"><title>Prey search behavior</title><p>The search behavior of Sycanus sp. during the initial phase – longer durations at first, then progressively shorter intervals – in line with the previous studies on predatory insects, which report that predators often search longer while familiarizing themselves with their environment and the spatial distribution of prey. The rapid decline in search time across subsequent prey encounters suggests that, once the predator located and captured its first prey, it finds additional targets more efficiently in the same arena. This pattern is in line with optimal foraging theory, which holds that predators adjust their search tactics according to previous encounters and environmental cues (<xref ref-type="bibr" rid="BIBR-28">Yuliadhi et al. 2021</xref>; <xref ref-type="bibr" rid="BIBR-22">Srikumar et al. 2014</xref>).</p><fig id="figure-3"><label>Figure 3</label><caption><p>Daily mortality of Metisa plana from predation by Sycanus sp.</p></caption><graphic xlink:href="https://www.jurnal.pei-pusat.org/index.php/jei/article/download/995/673/9638" mime-subtype="jpeg" mimetype="image"><alt-text>Figure 3</alt-text></graphic></fig><fig id="figure-4"><label>Figure 4</label><caption><p>Relationship between predator density and prey consumption by Sycanus sp. Values are presented as mean ± SE (n = 10).</p></caption><graphic xlink:href="https://www.jurnal.pei-pusat.org/index.php/jei/article/download/995/673/9639" mime-subtype="jpeg" mimetype="image"><alt-text>Figure 4</alt-text></graphic></fig><p>The ability of Sycanus sp. to adjust its search strategy upon detecting M. plana could strengthen its role in biological pest control in oil palm plantations. Such flexibility is likely important in agricultural systems, where fluctuating pest populations may demand varied predation strategies <xref ref-type="bibr" rid="BIBR-16">(Jamian et al. 2017)</xref>. Because a predator’s search behavior can shift with environmental complexity and with successive prey encounters, further should examine how prey density and habitat affect search efficiency; more complex environments, in particular, may hinder prey detection and lengthen the search process <xref ref-type="bibr" rid="BIBR-2">(Ahmad et al. 2020)</xref>.</p><p>The initial search time is a useful indicator of predator’s potential to control a pest. The shorter search times at higher predator densities may reflect density-dependent interactions among predators, although these were not measured directly. Such effects are likely more pronounced in confined laboratory settings than in the field, where predators and prey are distributed more heterogenously (<xref ref-type="bibr" rid="BIBR-23">Stone et al. 2023</xref>; <xref ref-type="bibr" rid="BIBR-16">Jamian et al. 2017</xref>).</p></sec><sec id="sec-13"><title>Prey handling time</title><p>The narrow range of handling times across all predator densities (58.1–59.1 minutes for 10 M. plana) indicates that prey handling in Sycanus sp. is governed mainly by physiological and behavioral traits intrinsic to the predator, rather than by external factors such as intraspecific competition (<xref ref-type="bibr" rid="BIBR-26">Ullah et al. 2019</xref>; <xref ref-type="bibr" rid="BIBR-22">Srikumar et al. 2014</xref>). The mode of prey immobilization employed by Sycanus sp.—piercing the larval cuticle and extracting body fluids through rostral sucking—is characteristic of the Reduviidae family and matches the mechanisms documented for other harpactorine assassin bugs (<xref ref-type="bibr" rid="BIBR-26">Ullah et al. 2019</xref>; Hwang &amp; Weirauch 2012). This piercing-sucking action causes progressive desiccation and death, and the emergence of M. plana larvae from their sacs provides a reliable behavioral indicator of successful predation.</p><p>The stability of handling time across predator densities contrasts with reports of density-related behavioral effects in some predatory insects, where prey exploitation varies with predator abundance. This constancy suggests that prey capture and consumption are constrained mainly by the physiological processes of immobilizing and feeding on prey rather than by predator density <xref ref-type="bibr" rid="BIBR-26">(Ullah et al., 2019)</xref>. This is also seen in other reduviid predators in which handling time remains relatively constant across different prey densities (<xref ref-type="bibr" rid="BIBR-28">Yuliadhi et al. 2021</xref>; <xref ref-type="bibr" rid="BIBR-2">Ahmad et al. 2020</xref>).</p><p>Handling time has important implications for biological control. Rapid, predictable handling lets Sycanus sp. process prey quickly and sustain a high predation rate, even in the highly modified environments of oil palm plantations, which supports its integration into an oil palm pest management plan <xref ref-type="bibr" rid="BIBR-27">(Wood 2019)</xref>. Optimizing the density and release timing of the predator could further improve prey suppression. As reported, for other harpactorine reduviids such as Cydnocoris gilvus (Burmeister) preying on Helopeltis antonii Signoret, in which handling time was a key determinant of predation efficiency <xref ref-type="bibr" rid="BIBR-22">(Srikumar et al. 2014)</xref>.</p></sec><sec id="sec-14"><title>Temporal dynamics of predation and mortality</title><p>The mortality of M. plana peaked on the first DAA and decline steadily across all predator-to-prey ratios, mirroring the acclimatization of Sycanus sp. after introduction to the experimental arena. The peak was more pronounced at the highest-density, where Sycanus sp. consumed nine M. plana larvae on the first day. This early surge likely results from a combination of hunger (from the 12 h pre-experimental starvation) and the stimulus of newly presented prey in a novel setting, which together trigger exploratory and predatory behavior (<xref ref-type="bibr" rid="BIBR-14">Imboma et al. 2020</xref>; <xref ref-type="bibr" rid="BIBR-26">Ullah et al. 2019</xref>).</p><p>The subsequent decline in feeding is consistent with reports that predators feed less after initial prey exposure, owing to satiation or reduced prey availability (<xref ref-type="bibr" rid="BIBR-28">Yuliadhi et al. 2021</xref>; <xref ref-type="bibr" rid="BIBR-26">Ullah et al. 2019</xref>). This “predation surge” – elevated predation rates immediately after introduction, followed by stabilization into a more sustainable feeding rhythm– has been described for other biocontrol agents (<xref ref-type="bibr" rid="BIBR-26">Ullah et al. 2019</xref>; <xref ref-type="bibr" rid="BIBR-16">Jamian et al. 2017</xref>). It indicates Sycanus sp. Exerts its strongest suppression right after release.</p></sec><sec id="sec-15"><title>Density-dependent effects on predation efficiency</title><p>Our results indicate predator density had a strong positive effect on the consumption of M. plana larvae by Sycanus sp. As predicted by ecological theory, more predators produced greater total prey mortality, indicating substantial potential for Sycanus sp. to suppress bagworm populations in oil palm systems at adequate densities (<xref ref-type="bibr" rid="BIBR-20">Siallagan et al. 2022</xref>; <xref ref-type="bibr" rid="BIBR-16">Jamian et al. 2017</xref>). However, the increase was not proportional; prey consumption rose about 3.5- fold across a fivefold increase in predator density, suggesting density-dependent interactions among predators that may influence prey consumption at higher densities. The regression, which explained over 95% of the variation in prey consumption, indicates a highly predictable predator–prey response under the tested conditions and suggests practical value for anticipating suppression from predator abundance in managed habitats <xref ref-type="bibr" rid="BIBR-1">(Adhikary et al. 2025)</xref>.</p><p>Our findings are in line with previous work on reduviid predators, including Sycanus dichotomus Stål and Cosmolestes picticeps (Stål), in suppressing bagworm populations in oil palm ecosystems <xref ref-type="bibr" rid="BIBR-2">(Ahmad 2020)</xref>, and with reports in other predatory Hemiptera where higher predator density enhances encounter rates and prey mortality. Because the per-capita gain diminished at higher densities, the highest prey mortality (at the 5:10 ratio) did not translate into proportionally greater consumption. The intermediate ratio of 2:10 may therefore offer a practical compromise between suppression and the number of predators deployed, although this requires field validation. From a management perspective, maintaining adequate populations of Sycanus sp. could enhance M. plana suppression and support the integration of this predator into sustainable integrated pest management (IPM) programs to reduce reliance on insecticides (<xref ref-type="bibr" rid="BIBR-12">Ikhsan 2024</xref>; <xref ref-type="bibr" rid="BIBR-27">Wood 2019</xref>; <xref ref-type="bibr" rid="BIBR-18">Priwiratama et al. 2018</xref>).</p></sec><sec id="sec-16"><title>CONCLUSION</title><p>Sycanus sp. showed effective predatory performance against M. plana under laboratory conditions: search efficiency improved after first prey encounter, handling time remained relatively constant across densities, and mortality was highest on the first day after exposure. Increasing predator density enhanced both prey mortality and consumption, though individual consumption rates declined at higher predator densities. Among the densities tested, a ratio of two Sycanus sp. adults per ten M. plana larvae offer a practical balance between prey suppression and predator use. These findings clarify the behavioral mechanisms underlying predation by Sycanus sp. and support its potential as a biological control agent for sustainable bagworm in oil palm plantations. Further field-based studies are needed to validate these laboratory findings.</p><p>PLoS ONE. 7:e45523. DOI: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1371/journal.pone.0045523" xlink:title="DOI link">DOI link</ext-link></p></sec></body><back><ack><title>ACKNOWLEDGEMENT</title><p>The authors gratefully acknowledge the valuable assistance and cooperation of the farmers and colleagues who supported this research. 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