Next Article in Journal
Genetic Characterization and Mating Disruption in Spodoptera Species, a Case Study on Spodoptera frugiperda (Lepidoptera, Noctuidae): A Systematic Review
Previous Article in Journal
Correction: Santori et al. Impact of Salmonella enteritidis Infection and Mechanical Stress on Antimicrobial Peptide Expression in Hermetia illucens. Insects 2025, 16, 692
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Sustainable Insect Pest Management Options for Rice Production in Sub-Saharan Africa

1
M’bé Research Station, Africa Rice Center (AfricaRice), Bouake 01 BP 2551, Côte d’Ivoire
2
Texas A&M AgriLife Research and Extension Center, 1509 Aggie Dr., Beaumont, TX 77713, USA
3
AfricaRice Nigeria Country Office, c/o IITA, Ibadan PMB 5320, Oyo State, Nigeria
4
IITA-Benin, Tri Postal, Cotonou 08 BP 0932, Benin
5
International Maize and Wheat Improvement Center (CIMMYT), ICRAF Campus, United Nations Avenue, Gigiri, Nairobi P.O. Box 1041-00621, Kenya
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Insects 2025, 16(11), 1175; https://doi.org/10.3390/insects16111175
Submission received: 31 August 2025 / Revised: 19 October 2025 / Accepted: 22 October 2025 / Published: 18 November 2025
(This article belongs to the Section Insect Pest and Vector Management)

Simple Summary

Major insect pests such as stem borers, leafhoppers, and rice bugs are increasingly threatening rice production in Sub-Saharan Africa (SSA). Sustainable pest management is vital to protect yields and promote agricultural sustainability. Integrated Pest Management (IPM) offers a balanced approach, combining multiple pest management strategies to reduce reliance on chemical inputs and safeguard ecosystems. Key strategies include weed and alternative host plant control, which limits pest habitats, and the use of resistant or tolerant rice varieties that naturally deter insect damage. Biopesticides—derived from natural organisms—are emerging as eco-friendly alternatives to synthetic chemicals. While chemical control remains common, its overuse can harm beneficial insects and the environment. Biological control, using predators and parasitoids, supports long-term pest suppression. A comparison between cultural, chemical, and biological methods demonstrates the value of context-specific solutions tailored to local farming systems. Advances in biotechnology, such as genetic resistance and molecular diagnostics, offer promising tools for future pest management. However, challenges persist, including limited farmer awareness, infrastructure gaps, and climate variability. Future directions should focus on farmer education, policy support, and adaptive research to strengthen sustainable pest management in SSA and ensure resilient rice production systems.

Abstract

Rice production in Sub-Saharan Africa (SSA) faces significant challenges due to insect pest infestations, which threaten food security and farmer livelihoods. This review examines the major insect pests affecting rice in SSA and highlights sustainable management strategies, drawing on successful case studies. It explores successful methods, including the use of biological control agents in Nigeria; neem-based pesticides in Tanzania; push-pull technology in Kenya; agroecological practices in Mali; resistant rice varieties in Ghana and Nigeria; integrated farming systems in Liberia, Guinea Conakry, Nigeria, Kenya and Madagascar; and farmer field schools in Zambia. Emerging technologies such as biotechnology and precision agriculture offer further additional opportunities to enhance pest control when effectively integrated within existing IPM frameworks. However, financial constraints, limited awareness, policy-related challenges, and inadequate infrastructure continue to limit widespread adoption. In this context, the review identifies critical research gaps, including the need for region-specific solutions, improved biopesticides, and long-term assessment of sustainable practices. Policy recommendations call for greater government investments, capacity-building programs, supportive regulatory environments, and stronger collaboration among researchers, development partners, and local stakeholders. Addressing these challenges can foster resilient and sustainable rice production systems across SSA.

1. Introduction

Rice is a crucial staple crop in Sub-Saharan Africa (SSA), playing an important role in food security and economic stability [1]. Insect pests are among the major challenges in rice production in SSA, causing significant yield losses and economic damage [2]. Common pests include the African rice gall midge (Orseolia oryzivora, AfRGM), rice stem borers, the grain stink bug (Aspavia armigera), and various species of planthoppers and leafhoppers [3,4,5]. These pests can reduce yields by up to 50%, severely impacting food security and farmer incomes [6]. Several factors, such as climatic conditions, cropping practices, and the availability of natural enemies, influence the presence and impact of insect pests [6]. In many regions, the absence of effective pest management tactics and lack of awareness of Integrated Pest Management (IPM) principles and practices exacerbate the problem, leading to recurrent pest outbreaks [6,7]. Additionally, the limited access to pest control resources and extension services among smallholder farmers hinders the adoption of IPM tactics. Addressing these challenges ensures that natural enemies and varietal resistance can be successfully used together during a cropping cycle to bring down pest damage to the crop.
IPM begins with accurate pest identification to learn about its biology and then build a successful management program to control it. This knowledge is essential for developing targeted, effective control strategies. Consistent monitoring of pest populations (e.g., Spodoptera frugiperda, Nymphula depunctallis, Trichispa spp., etc.) and their behaviors is vital for early detection of potential outbreaks and timely intervention to prevent large-scale damage. Furnishing farmers with knowledge, training, and skills in IPM techniques is crucial for successful implementation. IPM emphasizes the use of sustainable practices that minimize environmental impact and promote the long-term health of the agricultural system. Such sustainable practices include the combined use of biological, cultural, and mechanical control methods to minimize pest damage while reducing the reliance on synthetic pesticides [8,9]. Biological control involves the use of natural enemies, such as predators and parasitoids, to manage pest populations, while cultural practices involve the purposeful management of the crop environment to keep pest populations below harmful levels. These practices include crop rotation, intercropping, destruction of alternative host plants, and the use of resistant varieties [9,10]. Mechanical control methods, such as handpicking and the use of traps or barriers, are also employed [11]. However, the use of synthetic pesticides remains common due to their immediate effectiveness [12,13]. Their overuse and misuse have serious consequences, including the development of pesticide-resistant pest populations, environmental contamination, and health risks to farmers and consumers [14,15]. Therefore, promoting IPM practices and reducing the dependence on synthetic pesticides is crucial for sustainable pest management in rice production [16,17].
The purpose of this review is to provide a thorough review of the major insect pests affecting rice production in SSA and examine the various pest management strategies employed, with a particular focus on varietal resistance, cultural practices, biological control, IPM tactics and their effectiveness in reducing pest-related losses. Additionally, the review discusses the implications of chemical pesticide use and underscores the need to implement sustainable and environmentally friendly pest control methods. By addressing these key areas, the review seeks to support the development of effective and sustainable pest management practices, inform future policy formulation, promote the adoption of effective IPM practices, and ultimately contribute to enhance rice productivity and food security in SSA.

2. Insect Pests in SSA Rice Production

2.1. Common Insect Pests of Rice in SSA

Rice production in SSA is threatened by a wide range of insect pests, which can cause massive yield losses (10–50%), depending on the pest species, crop stage, and management practices [18,19]. Among the most damaging is the African rice gall midge (Orseolia oryzivora Harris & Gagné) which induces gall formation on rice plants, stunting growth and reducing yields [20]. Other pests include stem borers, such as the African white borer (Maliarpha separatella Ragonot) and the pink borer (Sesamia calamistis Hampson), which bore into rice stems, triggering symptoms such as deadhearts and whiteheads, both of which lead to considerable yield reductions [21,22]. Another important pest is Aspavia armigera Fabricius, also known as the shield bug (grain stink bug), which affects rice grain quality. Infestations at the milk stage can cause up to 70% loss in grain weight and a significant drop in both paddy and head rice recovery [23]. Sap-sucking insects like the brown planthopper and leafhoppers, such as the green leafhopper (Nilaparvata lugens Stal), not only cause direct damage by sucking sap from rice plants but also act as vectors for viruses, such as rice yellow mottle virus and rice tungro virus [22,24].
Defoliators, such as armyworms and cutworms, reduce photosynthetic capacity and overall plant vigor by feeding on foliage [22,25]. The warm and humid climate of many SSA regions favors the rapid multiplication of these pests, often leading to widespread infestations [26,27]. Considering the complex interplay between environmental factors and pest dynamics in the region, effective management of these pests is crucial for ensuring sustainable rice production and food security in SSA. Table 1 shows the most important insect pests that impact rice production in SSA.

2.2. Pests Impact on Rice Yield and Quality

Insect pests pose a significant threat to rice production across SSA, with economic losses that can be both extensive and devastating. While average yield reductions range from 10 to 15%, some regions experience losses of up to 90% in severe infestations [6,46,47]. These reductions in yield translate to significant financial losses for farmers who rely on rice not only as a staple crop but also as a source of income [48,49].
Beyond yield losses, insect damage also deteriorates grain quality, decreasing market value and consumer acceptance [50,51]. According to the same authors, pests such as grain stink bugs, stem borers, and planthoppers cause discoloration and broken kernels and reduce nutritional value, all of which lower the commercial appeal of harvested rice.
Several studies across SSA demonstrate the widespread effects of pest infestations and highlight the urgent need for effective management strategies. For instance:
Nigeria and Ghana: The African rice gall midge (O. oryzivora) was reported to cause yield losses of up to 60%, leading to severe farm income reductions and increased pest control expenses [52]. Similar infestations were reported in Ghana, underscoring the critical need for improved pest management [53].
Tanzania and Kenya: Stem borers such as M. separatella and S. calamistis were responsible for yield losses ranging between 10% and 50%, coupled with increased pesticide and labor costs [54]. Research in Kenya found similar results indicating widespread pest impact and reiterated the importance of IPM in mitigating insect pest losses [55].
Benin: Defoliators, including armyworm [56].
Taken together, these case studies underscore the substantial burden insect pests place on rice production and farmer livelihoods in SSA. Table 2 shows the cumulative losses from pest infestations are estimated at USD$3 billion annually for maize, wheat, and rice [57].
Several pest species induce specific damage to rice while it grows. Figure 1 depicts various insects seen in African rice fields and the damage they cause to the fields.

3. Pest Management Strategies

3.1. Cultural Practices

For centuries, people have used traditional pest management practices to maintain healthy crops and reduce pest populations, often without relying on synthetic chemicals [104]. These methods are sustainable and environmentally friendly, making them valuable components of IPM systems.

3.1.1. Crop Rotation

This method disrupts the life cycles of pests that are specific to certain crops, reducing their populations over time. Evidence of its efficacy was demonstrated in rice, where crop rotation had improved soil health, crop yield, and pest control, using big data [105]. In the context of rice production across Sub-Saharan Africa (SSA), several countries have demonstrated the value of this practice in pest control. In Nigeria, rotating rice with cowpeas significantly reduced the population of rice stem borers [106]. In Tanzania, alternating rice with maize effectively managed rice leafhoppers) [107]. In Uganda, rotating rice with groundnuts helped to control the incidence of rice yellow mottle virus, often spread by insect vectors [107]. In Kenya, rotating rice with soybeans reduced the incidence of rice gall midge [108]. In Ghana, rotating rice with cassava proved successful in managing rice hispa infestations [108]. Beyond pest suppression, crop rotation contributes to soil fertility maintenance and the mitigation of soil-borne diseases [109]. These examples demonstrate how crop rotation is not only a key pest management strategy but also improves the overall agroecosystem resilience.

3.1.2. Intercropping

Intercropping serves as a valuable strategy for pest management by creating a more complex habitat that disrupts pest behavior and reduces their ability to locate their preferred host plants [110]. This practice can also attract beneficial insects, such as predatory insects and parasitoids that prey on pests, thereby providing natural pest control [111]. For instance, intercropping maize with legumes reduces the incidence of stem borers while improving overall crop resilience [112]. Additionally, the diversity of plant species in intercropping systems suppresses weed growth, which in turn reduces habitats that harbor crop pests [113]. In the context of rice, intercropping has been successfully employed as an insect pest management strategy across SSA. In Nigeria, intercropping rice with cowpeas significantly reduced rice stem borer population [114]. According to Himmelstein et al. (2017) [115], the results from a meta-analysis reveal positive impacts of intercropping on crop yield, farmers’ income, and the effect of integrated pest management in Africa. In Uganda, intercropping rice with groundnuts reduced the incidence of rice yellow mottle virus [116]. In Kenya, the practice of intercropping rice with soybeans has reduced the prevalence of rice gall midge [117]. According to Mugisa et al.’s 2000 [118] study on upland rice in Central Uganda, the 4:3 row intercrop ratio is preferred for rice-based intercrops with beans and groundnuts, whereas 3:2 is preferred for rice-maize intercrops. For Daryanto et al. [119], in terms of sustainable agriculture, intercropping can raise soil fertility, provide soil erosion and pest/weed management, and improve soil carbon sequestration without sacrificing land productivity. This understanding is critical given the connections between biotic and abiotic elements in agroecosystems (for example, maximizing sun radiation and periods). Overall, intercropping exemplifies a synergistic approach to sustainable pest management. By naturally lowering pest pressures and encouraging biodiversity, it reduces dependency on synthetic pesticides and enhances agroecosystem resilience. These benefits are especially critical in SSA, where smallholder farmers often have limited access to expensive synthetic inputs.

3.1.3. Manual Removal

Manual pest removal is one of the simplest and most direct methods of pest control. This technique involves physically removing pests from crops by hand or using tools. It is particularly effective for managing large, visible pests such as caterpillars, beetles, and slugs. It is labor-intensive but highly effective in small-scale farming or home gardens [120]. Complementary practices like pruning, weeding, and the destruction of infested plant material further contribute to reducing pest populations and preventing the spread of diseases [121,122]. While not scalable for large commercial farms, manual removal reduces the use of chemical pesticides, which helps to preserve biodiversity, safeguard soil and water quality, and promote healthier ecosystems [123]. Embedding these approaches within broader IPM programs ensures a balance between productivity and sustainability.

3.1.4. Destruction of Alternative Hosts and Volunteer Plants

Managing alternative host plants and weeds (unwanted plants in a specific setting) is a vital cultural strategy in the control of insect pests. Many alternative plant species serve as refuges or breeding grounds for insect pests, maintaining pest populations even in the absence of rice. By reducing or eliminating these alternative host plants, the lifecycle of pests is disrupted, leading to a decrease in their population and reduces the likelihood of damage to rice crops. In addition, by removing the “safe havens” pests rely on outside the main cropping season, farmers can dramatically reducing initial pest pressure. In Africa, notable examples include managing Striga in Kenya, weed suppression in Nigeria, and aquatic weed control in Lake Victoria. Biological strategies in Ethiopia and Ghana further highlight success [124,125]. Table 3 shows a few pests damaging rice production in Africa and their host plants. In Kenya, the International Center on Insect Physiology and Ecology (ICIPE) introduced push-pull technology, which uses a combination of repellent and attractant plants to manage stem borers and striga weeds in rice fields.

3.1.5. Use of Resistant/Tolerant Rice Varieties

The use of plant breeding to develop resistant rice varieties against insect pests is a crucial strategy for sustainable rice production in SSA. By leveraging the genetic diversity found in different rice cultivars, researchers can identify and incorporate resistance genes and quantitative trait loci (QTLs) that confer protection against major insect pests. For instance, the gene Bph3 provides resistance to the brown planthopper (N. lugens) by triggering the production of toxic secondary metabolites that deter feeding [151]. Likewise, Bph14 confers resistance by reinforcing cell walls and activating defense-related genes [152]. The Pi9 gene, mainly used to combat rice blast disease (Pyricularia oryzae), indirectly helps in reducing the population of stem borers that thrive in weakened plants [153]. Notable regional applications demonstrate the effectiveness of host plant resistance. For instance, the Makassane variety in Mozambique, which carries multiple resistance genes including Pi9 and Bph3, significantly reduces the incidence of both rice blast and brown planthopper infestations [154,155]. Similarly, in Nigeria, the deployment of the NERICA (New Rice for Africa) varieties, which possess QTLs such as qBph1 and qBph2, has improved resistance to the African rice gall midge (O. oryzivora) [156]. Adoption of resistant rice varieties has led to a significant reduction in pest infestations, with a reported 30% decrease in yield losses due to pests [26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152,153,154,155,156,157]. In Ghana, the use of WITA 4 variety, harboring the Bph18 gene, has proven effective against the brown planthopper [158]. In addition, adoption of resistant rice varieties, such as NERICA (New Rice for Africa), successfully controlled the African rice gall midge, resulting in higher productivity and reduced crop losses [159]. These examples highlight the importance of using resistant or tolerant rice varieties in IPM in SSA, where environmental challenges and resource constraints limit chemical use. Moreover, the use of plant resistance aligns with climate-smart and sustainable agriculture goals, preserving biodiversity, safeguarding human health, and supporting long-term productivity. Therefore, continued investment in breeding programs and local seed dissemination is essential to expand access to these resistant varieties and strengthen food systems across the region.
Below in Table 4, are a few genes identified in rice for resistance to insect pests and the exhibited resistance mechanisms.

3.2. Chemical Control

The use of synthetic pesticides remains one of the most common and effective methods for managing agricultural pests. These substances are specifically formulated to eliminate or deter insects, weeds, and pathogens, thereby protecting crops and enhancing yields. Studies suggest that without pesticide application, global agricultural output could be reduced by over 50% due to pest and disease damage [208]. Consequently, pesticides are considered critical tools for maintaining food security and stabilizing agricultural economies, particularly in regions vulnerable to high pest pressure [209]. In many rice-growing regions of Africa, farmers rely heavily on chemical insecticides to manage major pests such as stem borers, leaf feeders, and plant hoppers. These chemicals are often applied as foliar sprays (contact or systemic) when pest levels reach visible thresholds, or sometimes in calendar-based schedules in absence of monitoring. In West Africa, carbamates (e.g., carbaryl) and pyrethroids (e.g., lambda-cyhalothrin, Deltamethrin) are common [210,211]. Moreover, in Nigeria, the application of chlorpyrifos significantly reduces the population of rice stem borers, leading to increased yields [21]. In East Africa, synthetic pyrethroids and organophosphates are widely used. For instance, in Tanzania, the use of lambda-cyhalothrin has proven effective in managing rice leafhoppers [212]. In Uganda, farmers have successfully used imidacloprid to control the incidence of rice yellow mottle virus, transmitted by insect vectors [36]. In addition, the use of chemical insecticides to control the African rice gall midge led to a 60% reduction in pest populations [213]. In Kenya, the application of carbofuran reduced the prevalence of rice gall midge, resulting in healthier crops [214]. Across several African countries, fipronil has been deployed to manage rice hispa outbreaks [215]. Overall, chemical control offers rapid and cost-effective protection against pest outbreaks, especially during periods of high infestation. Table 5 summarizes a few synthetic pesticides commonly used in SSA rice farms.

3.3. Nature-Based Control Options

Nature-based control options, such as biological control, biopesticides, and semi-ochemicals, are characterized by their low impact on non-target organisms, as well as on human, animal, and environmental health.
Biological control is an environmentally sustainable approach that uses natural predators, parasitoids, and beneficial microorganisms to regulate pest populations [262,263]. This method leverages the natural relationships between organisms to reduce pest numbers without relying on chemical pesticides. In SSA, several successful field-level applications demonstrate effectiveness in managing insect pests in rice production. In Nigeria, the introduction of Trichogramma wasps, which parasitize rice stem borer eggs, significantly reduced pest populations [38]. In addition, the use of the predatory beetles in the family Coccinellides has proven effective in managing the rice yellow mottle virus, by reducing populations of the aphids vectors, leading to increased yields [264]. In Tanzania, the use of predatory beetles in the family Coccinellidae has helped control rice leafhoppers [265]. In addition, the use of entomopathogenic fungi to control the rice weevil has shown promising results, with a 40% pest mortality [5,266]. In Tanzania, the adoption of IPM strategies, including the use of neem-based biopesticides, has reduced the reliance on synthetic pesticides and improved the sustainability of rice farming [267]. Additionally, in Zambia, the implementation of farmer field schools has empowered local farmers with knowledge and skills to manage pests using environmentally friendly methods. In Uganda and Tanzania, the introduction of pheromone traps has been effective in managing rice stem borer populations, reducing the need for synthetic pesticides and increasing rice [21]. In Uganda, the application of beneficial fungi such as Beauveria bassiana has proven successful in managing rice hispa infestations [268]. In West Africa, the release of parasitoid wasps like Anagrus spp. helped to limit the prevalence of rice gall midge [269]. In Benin and Côte d’Ivoire, the fungus Neozygites tanajoa has effectively managed the cassava green mite, demonstrating its potential for broader pest management applications [270]. In Kenya, the introduction of parasitoid wasps to control the rice yellow stem borer resulted in a 50% reduction in pest populations and a corresponding increase in rice yields [38,271].
By reducing pest populations through natural regulation, these agents help maintain biodiversity, improve crop resilience, and minimize harm to non-target organisms. Continued investment in research, farmer training, and regional adaptation of biocontrol technologies is essential for scaling up their adoption.
Table 6 provides examples of biopesticides, natural predators, parasitoids, and beneficial microorganisms used to control insect pests.

3.4. Integrated Farming System

Integrated Farming System (IFS) is an ecologically sustainable approach that integrates crops, livestock, and other agricultural components to create a balanced, self-reliant production system [399]. Its goal is to enhance productivity and profitability while minimizing environmental impact and maximizing the efficient use of available resources [399].
A well-known example is the Integrated Rice-Fish (IRF) System, which has been practiced in Southeast Asia for over 2000 years. This method combines rice cultivation with managed fish farming, creating mutual benefits that improve soil health and reduce pest pressure [400]. This model has been implemented in different agroecological zones in Sub-Saharan Africa [401,402]. The results of the study conducted on IRF in Nigeria showed that it helped to eradicate weeds and harmful insects. The author concluded that Fish in the rice field serves as a biological control to reduce insects and some rice diseases [403].
In Kenya, the incidence of rice stem-borers was significantly reduced by 40% in the IRF system compared to rice monoculture because insect pests, including stem-borers, were eaten by fish [404].
In Liberia, Tilapia nilotica (Linnaeus, 1758) was used to significantly control mosquito larvae in the rice field [405], and in Guinea, the IRF system helped to reduce crop pests like caterpillars, rats, and agouti in the field [403,406,407]. It was concluded that this model can use fish as a safe and cheaper alternative to chemical pesticides.
A similar method is rice–duck systems, which utilize ducks to manage weeds and insect pests, effectively boosting rice yields [408]. Additionally, Chinese rice–frog systems, in which frogs serve as biological pest control agents, have helped reduce reliance on chemical fertilizers and pesticides, offering an environmentally sound alternative to conventional farming [409].
By promoting nutrient recycling, natural pest control, and diversified income sources, IFS fosters long-term resilience in agricultural landscapes.

3.5. Summary of the Strengths and Limitations of Cultural, Biological, and Chemical Control

Insect pest management in rice production across SSA involves cultural, biological, and chemical control methods, each with distinct advantages and limitations.
Cultural control aims to disrupt pest life cycles and reduce pest populations by altering the environment [410,411]. This method is environmentally sustainable: they reduce reliance on synthetic inputs, supporting soil health and biodiversity. Secondly, it’s cost-effective over time and requires minimal external input once practices are well established. However, the method also presents some limitations, including delayed impact: it often takes multiple seasons before benefits are fully realized and may require significant changes in farming practices [412,413]. Behavioral and systemic barriers involve the requirement for education, training, and long-term adoption by farming communities, and Site-specific effectiveness may be a factor as it may not control pests uniformly across different agroecological zones and may require significant changes in farming practices and longer timeframes to see results.
Biological control methods involve the use of natural enemies, such as predators, parasitoids, and pathogens, to manage pest populations. This method is target-specific: natural enemies focus on specific pests, minimizing harm to beneficial organisms. Once established, populations of natural enemies can regulate pests over time. Moreover, it’s environmentally friendly, posing minimal risk to ecosystems and human health. However, the method also presents some limitations, including climate sensitivity: efficacy can be influenced by temperature, humidity, and habitat conditions [414,415]. It also has scientific complexity as it requires research, monitoring, and technical expertise for successful implementation, and a slower response as this method may not provide immediate pest suppression during outbreaks.
Chemical control methods utilize synthetic insecticides that are fast acting in suppressing pest populations. Advantages include being Fast and effective, as it delivers immediate pest knockdown, especially during high-pressure outbreaks, and widely available as products are accessible and easy to apply with existing tools and predictable results. Farmers often see measurable short-term yield gains. However, the methods present limitations, including resistance development: overuse can lead to resistant pest populations, reducing their long-term efficacy; additionally, it may cause environmental contamination, with risks including water, soil, and air pollution, and non-target effects as it can harm beneficial insects, wildlife, and human health if misused [209].
The optimal pest management strategy depends on site-specific conditions, the pest species involved, farmer resources, and long-term sustainability goals. Integrating these methods through IPM can maximize their strengths and minimize their weaknesses, leading to more effective and sustainable pest management [416,417]. Table 7 highlights the pest management methods.

3.6. Limitations of Conventional and Chemical Methods in Rice Insect Pest Management

Traditional rice insect control methods such as crop rotation, manual removal, and field sanitation often show limited effectiveness when applied in isolation [27]. Crop rotation may fail where alternative hosts of key pests persist nearby or where small landholdings constrain rotation options [418]. Manual removal and handpicking are labor-intensive and impractical for large fields or high pest infestations [419], while cultural practices like flooding or synchronized planting are influenced by water availability, labor, and farmer coordination [420]. Their success also depends on the pest’s biology, environmental conditions, and farmers’ awareness and timing of application. Similarly, reliance on chemical control presents several disadvantages: repeated use can lead to pest resistance, resurgence, and elimination of natural enemies, disrupting ecological balance. the widespread use of chemical pesticides in rice production across SSA results in a range of negative outcomes for human health, animal well-being, and environmental sustainability [421]. Inappropriate handling and overuse of pesticides—often due to limited training and lack of protective equipment—have exposed farmers to acute health issues such as headaches and respiratory disorders [422]. Yarpuz-Bozdogan 2018 [423] revealed that in Cameroon, Ethiopia, Ghana, and Nigeria, almost 33%, 14%, 28%, and 38% of people used masks during pesticide application, with the combined prevalence of glove use being 8%, 12%, 31%, and 51% in those same countries. Furthermore, about 23% of empty pesticide containers were reused in Benin, 26% in Egypt, 31% in Ethiopia, 21% in Ghana, 30% in Nigeria, and 9% in Tanzania. Beyond human exposure, pesticide runoff into nearby water bodies has been shown to harm aquatic ecosystems and reduce biodiversity, affecting fish and other non-target organisms that are vital to rural livelihoods [424]. Additionally, pesticide residues in rice pose food safety risks. Studies have detected organochlorine pesticide residues in locally processed rice in Nigeria, including compounds like endrin and aldrin, which, although within maximum residue limits, still raise concerns about chronic exposure [424]. These residues can bioaccumulate in animals and humans, potentially leading to long-term health effects such as endocrine disruption and cancer [425]. The lack of regulatory enforcement and continued use of unauthorized or highly hazardous pesticides further exacerbate these risks [426]. An integrated pest management (IPM) approach combining cultural, biological, and chemical tools is therefore essential for long-term effectiveness.

4. Innovative Approaches and Technologies

4.1. Advances in Biotechnology

Biotechnological innovations have revolutionized pest management in rice through tools such as genetic engineering, CRISPR genome editing, and RNA interference (RNAi). These technologies offer precise and durable solutions for managing insect pests, reducing reliance on synthetic pesticides. For instance, the incorporation of the Bt gene from Bacillus thuringiensis into rice has conferred resistance to stem borers [153]. CRISPR technology has enhanced pest resistance by allowing precise editing of rice genomes to knock out susceptibility genes or introduce resistance traits [187]. Additionally, RNA interference (RNAi) has been employed to silence essential genes in pests, reducing their ability to damage rice plants [427].

4.2. Precision Agriculture

Precision agriculture leverages advanced technologies such as sensors, drones, and data analytics to monitor and manage pest populations effectively. Drones with imaging technology are being deployed for rice production in Ghana, where farmer cooperatives are using drones for crop monitoring and input management [427]. Sensors placed in rice fields can detect early signs of pest infestations by monitoring environmental conditions and plant health [428,429]. Drones equipped with high-resolution cameras and multispectral sensors provide real-time aerial imagery, enabling farmers to identify pest hotspots and assess crop health [430]. Data analytics tools process this information to generate actionable insights, allowing for targeted interventions and optimized pesticide use [431]. McCarthy et al., 2023 and Raheem et al., 2021 [432,433] mentioned the use of drones by some African farmers.

4.3. Ecological Engineering

Ecological engineering involves habitat manipulation and landscape management to enhance natural pest control. By creating habitats that support natural enemies of pests, such as predators and parasitoids, farmers can reduce pest populations naturally [434]. Key practices include the use of cover crops, maintaining hedgerows, and creating buffer zones that provide refuges and alternative food sources for beneficial insects [435]. Additionally, landscape management practices, such as crop rotation and intercropping, disrupt pest life cycles and reduce their impact on rice crops [111,436]. In Mali, agroecological practices like crop rotation and intercropping with legumes have enhanced pest management by improving soil health and biodiversity, which naturally controls pest populations [437,438]. These case studies highlight the diverse and innovative approaches being used across SSA to tackle pest challenges in rice production. They align seamlessly with the principles of IPM, promoting biodiversity, reducing chemical inputs, and strengthening the resilience of agroecosystems.

5. Case Studies and Lessons Learned

Success stories from various countries in SSA offer valuable lessons and best practices for sustainable pest management. Throughout this work, we have highlighted case studies demonstrating the effective use of diverse methods and IPM strategies. Noteworthy examples include:
The push-pull technology was developed by ICIPE in Kenya, which combines trap plants to attract Spodoptera frugiperda and repellent intercrops to deter it. This technology is cited as an ideal approach for mixed farming systems, effectively reducing S. frugiperda larval density and damage to cereals crops [439].
An important yet previously unmentioned case is the use of farmer field schools in Burkina Faso, Mali, Zambia, Malawi by FAO, and IFAD to empower local farmers with the knowledge and skills needed to manage pests using environmentally friendly methods. This case highlights a critical lesson: community involvement and capacity building are fundamental to the success and sustainability of IPM. Additionally, strong collaboration between research institutions and farming communities, as seen in Nigeria, significantly enhances the adoption and effectiveness of pest management strategies [264]. These case studies emphasize the importance of a holistic and inclusive approach to pest management in SSA. Scaling these lessons across the region has the potential to strengthen low-input, resilient farming systems that uphold both food security and environmental integrity.

6. Challenges and Future Directions

6.1. Barriers to Adopting Sustainable Practices

Economically, many smallholder farmers lack the financial resources to invest in sustainable technologies and practices, such as biopesticides or pheromone traps [10]. Socially, there is often a lack of awareness and education about sustainable practices, leading to a preference for conventional chemical pesticides [440,441]. Additionally, cultural beliefs and traditional farming practices hinder the acceptance of new methods [33]. On the technical front, several obstacles remain. The availability of sustainable pest control inputs is often restricted, and distribution networks are either underdeveloped or entirely lacking in remote areas. Compounding these issues is the variability of pest pressures and environmental conditions across regions, making it difficult to design and implement one-size-fits-all strategies.

6.2. Research Gaps and Future Research Needs

Addressing the challenges of sustainable pest management in SSA requires integrating ecological, socio-economic, and health aspects using frameworks like System Thinking and Digital Twins for dynamic, data-driven pest management. A critical knowledge gap exists due to poor understanding of the factors that trigger pest outbreaks and limited tools for accurate predictions. One critical research gap lies in developing locally adapted pest control solutions that reflect the diverse ecological zones and socio-economic realities across SSA [10]. Tailored approaches are essential to ensure effectiveness and farmer acceptance. Research is also needed to improve the efficacy, affordability, and scalability of biopesticides and other eco-friendly products [440]. Many sustainable products remain out of reach for smallholder farmers due to cost or limited distribution. In Mali, a participatory framework helped farmers prioritize climate-smart IPM innovations across four rice ecologies, enhancing local adaptation and institutional support [442]. AfricaRice’s Participatory Learning and Action Research (PLAR) approach in Nigeria and Côte d’Ivoire empowered farmers to co-develop integrated rice management strategies, improving pest control and productivity in inland valleys [443]. Studies in Uganda showed that training participants effectively transferred IPM knowledge to peers, amplifying adoption and community ownership [444]. There is a need for joint participatory methods in developing and adopting IPM technologies because they foster farmer empowerment, community ownership, greater social acceptance and knowledge-intensive farming systems.

6.3. Recommendations and Policy Support Mechanisms

To accelerate the adoption of sustainable pest management practices in SSA, national governments should develop and implement enabling policies and targeted supportive mechanisms. Key recommendations include the following:
Providing financial incentives, such as subsidies for sustainable products, including biopesticides, pheromone traps, and resistant seed varieties, as well as access to low-interest loans. Such measures can help alleviate the economic burden on smallholder farmers [10].
Investment in training and extension services, which is critical to raise awareness and build the capacity of farmers to adopt and implement sustainable techniques effectively [440,445].
Support for research and development. This should be prioritized to produce context-specific, locally adapted pest control solutions and improve the accessibility of sustainable products [33,446].
Regional and international collaboration with research institutions, development agencies, and NGOs. This can facilitate knowledge exchange, innovation, and funding mobilization.
Regulatory frameworks must be strengthened to restrict the use of highly hazardous pesticides and promote safer, more sustainable alternatives.
Policy plays a pivotal role in shaping the trajectory of agricultural innovation. In SSA, where pest pressure is high and farm-level resources are often limited, these recommendations point to a roadmap for transformative change. By lowering financial hurdles and increasing farmer access to information and technologies, policymakers can empower rural communities to transition from chemical-heavy approaches to resilient, low-input farming systems. Moreover, regulation isn’t just about restriction; it’s also about direction. Clear, science-based policies can create an enabling environment where safer products reach the market, research aligns with farmer needs, and innovation is rewarded. Therefore, strengthening the link between public policy, scientific research, and grassroots practice is essential for building an agroecologically sound and food-secure future.

7. Conclusions

This review has highlighted various successful pest management practices across different regions in SSA, emphasizing the importance of IPM strategies. Studies from countries such as Kenya, Nigeria, Tanzania, Ghana, Mali, Benin, Uganda, Liberia, Guinea Conakry, Madagascar, and Zambia have demonstrated the effectiveness of diverse approaches. These practices have led to increased rice yields, reduced reliance on synthetic chemicals, and improved sustainability. However, the adoption of these practices faces economic, social, and technical challenges, ranging from limited financial resources and inadequate infrastructure to insufficient farmer awareness and education. Nevertheless, the collective evidence suggests that overcoming these barriers can unlock significant benefits in rice productivity and food security. The success stories highlighted offer a practical framework for designing and scaling effective, locally adapted pest management strategies. Integrating multiple approaches, such as combining biological controls with cultural practices, can improve system resilience and promote long-term sustainability. Looking ahead, it is critical for stakeholders to support the development and dissemination of region-specific pest control solutions. Governments should implement enabling policies that offer financial incentives, access to training, and investment in agricultural extension services. Equally important is the role of collaboration between researchers, international organizations, and local farming communities to foster innovation and knowledge exchange. Finally, strengthening regulatory frameworks to promote sustainable practices and restrict hazardous chemical use is crucial. By adopting a holistic and inclusive approach, SSA can build resilient rice production systems that support both environmental health and rural livelihoods for generations to come.

Author Contributions

E.P.: Validation, Writing—original draft, Writing—review, Funding acquisition & editing. R.B.: Resources, Writing—original draft, Validation, Writing—review & editing. G.O.: Validation, Writing—original draft. F.N.: Validation, Writing—review & editing. M.T.: Validation, Writing—review & editing. A.T.: Validation, Writing—review & editing. S.K.K.: Validation, Writing—review & editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

The authors express their profound gratitude to the AfricaRice Center (AfricaRice) for sponsoring this paper, highlighting the center’s essential efforts to disseminate knowledge and scientific innovations for reducing insect pests in rice and improving global food security. They also thank IRRI and Georg Goergen from IITA for allowing them to use their pictures of insects in this manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Wopereis, M.C.S.; Johnson, D.E.; Ahmadi, N.; Tollens, E.; Jalloh, A. Realizing Africa’s Rice Promise; CAB International: Wallingford, UK, 2013; p. 451. [Google Scholar]
  2. Bekele, B.G. Review on integrated pest management of important disease and insect pest of rice (Oryza sativa L.). World Sci. News 2018, 100, 184–196. [Google Scholar]
  3. Heinrich; Nwilene, F.; Stout, M.; Hadi, B.; Freitas, T. Rice Insect Pests and Their Management; Burleigh Dodds Science Publishing: London, UK, 2017; p. 292. [Google Scholar] [CrossRef]
  4. Joda, A.O. Developmental biology of Aspavia armigera (Fabricius, 1775) (Hemiptera: Pentatomidae) on rice (Oryza sativa L.) (Poaceae) and three other hosts in Nigeria. Pol. J. Entomol. 2019, 88, 349–361. [Google Scholar] [CrossRef]
  5. Bonaventure, J. Management Options for Rice Stem Borers in Irrigated Low Land Rice Ecosystems in Tanzania. Ph.D. Thesis, Sokoine University of Agriculture, Morogoro, Tanzania, 2020. [Google Scholar]
  6. Saito, K.; Senthilkumar, K.; Dossou-Yovo, E.R.; Ali, I.; Johnson, J.M.; Mujawamariya, G.; Rodenburg, J. Status quo and challenges of rice production in Sub-Saharan Africa. Plant Prod. Sci. 2023, 26, 320–333. [Google Scholar] [CrossRef]
  7. Heeb, L.; Jenner, E.; Cock, M.J.W. Climate-smart pest management: Building resilience of farms and landscapes to changing pest threats. J. Pest Sci. 2019, 92, 951–969. [Google Scholar] [CrossRef]
  8. Tiwari, A.K. IPM Essentials: Combining Biology, Ecology, and Agriculture for Sustainable Pest Control. J. Adv. Biol. Biotechnol. 2024, 27, 39–47. [Google Scholar] [CrossRef]
  9. Baker, B.P.; Green, T.A.; Loker, A.J. Biological control and integrated pest management in organic and conventional systems. Biol. Control 2020, 140, 104095. [Google Scholar] [CrossRef]
  10. van Huis, A. Challenges of integrated pest management in Sub-Saharan Africa. In Integrated Pest Management: Dissemination and Impact; Peshin, R., Dhawan, A.K., Eds.; Springer: Dordrecht, The Netherlands, 2009; Volume 2, pp. 395–417. [Google Scholar]
  11. Adhikari, U. Insect Pest Management: Mechanical and Physical Techniques. Rev. Food Agric. 2022, 3, 48–53. [Google Scholar] [CrossRef]
  12. Peralta, M.P.; Palma, J.L. Rice Production without Insecticide in Smallholder Farmer’s Field. Front. Environ. Sci. 2017, 5, 16. [Google Scholar] [CrossRef]
  13. Fenibo, E.O.; Ijoma, G.N.; Matambo, T. Biopesticides in Sustainable Agriculture: A Critical Sustainable Development Driver Governed by Green Chemistry Principles. Front. Sustain. Food Syst. 2021, 5, 619058. [Google Scholar] [CrossRef]
  14. Zhou, W.; Li, M.; Achal, V. A comprehensive review on environmental and human health impacts of chemical pesticide usage. Emerg. Contam. 2024, 11, 100410. [Google Scholar] [CrossRef]
  15. Abaineh, A.; Ejigu, D.; Atlabachew, M.; Dejen, E.; Tilahun, G. Pesticides in use, their application and risks on human health and ecosystems: A case of Fogera District, Ethiopia. Sustain. Environ. 2024, 10, 2298063. [Google Scholar] [CrossRef]
  16. Constantine, K.L.; Kansiime, M.K.; Mugambi, I.; Nunda, W.; Chacha, D.; Rware, H.; Makale, F.; Mulema, J.; Julien Lamontagne-Godwin, J.; Williams, F.; et al. Why don’t smallholder farmers in Kenya use more biopesticides? Pest Manag. Sci. 2020, 76, 3615–3625. [Google Scholar] [CrossRef]
  17. Rodenburg, J.; Johnson, J.M.; Dieng, I.; Senthilkumar, K.; Vandamme, E.; Akakpo, C.; Allarangaye, M.D.; Baggie, I.; Bakare, S.O.; Bam, R.K.; et al. Status quo of chemical weed control in rice in Sub-Saharan Africa. Food Secur. 2019, 11, 69–92. [Google Scholar] [CrossRef]
  18. Horgan, F.G.; Srinivasan, T.S.; Crisol-Martínez, E.; Almazan, M.L.P.; Ramal, A.F.; Oliva, R.; Quibod, I.L.; Bernal, C.C. Integrated pest management for rice in Africa: Past, present, and future. Outlooks Pest Manag. 2021, 32, 77–86. [Google Scholar]
  19. Osasona, K.K.; Akinsola, G.B.; Salami, M.F.; Adebisi, L.O.; Adebisi, O.A.; Fashola, O. Sustainable agricultural practices and related problems among rice farming households in Kwara State, Nigeria. Cercet. Agron. Mold. (Agron. Res. Mold.) 2020, 52, 399–409. [Google Scholar] [CrossRef]
  20. Ouattara, D.; Nacro, S.; Latévi, K.; Coulibaly, A.; Somda, I. Ecology of the African Rice Gall Midge, Orseolia oryzivora in Western Burkina Faso. Adv. Entomol. 2020, 8, 1–14. [Google Scholar] [CrossRef]
  21. January, B.; Rwegasira, G.M.; Tefera, T. Impacts of plant spacing and nitrogen fertiliser on incidences and density of spotted and African pink stem borers in Tanzania. Int. J. Pest Manag. 2020, 67, 241–251. [Google Scholar] [CrossRef]
  22. Akinsola, E.A.; Agyen-Sampong, M. The ecology, bionomics and control of rice stem-borers in West Africa. Int. J. Trop. Insect Sci. 1984, 5, 69–77. [Google Scholar] [CrossRef]
  23. Bhavanam, S.; Wilson, B.; Blackman, B.; Stout, M. Biology and management of the rice stink bug (Hemiptera: Pentatomidae) in rice, Oryza sativa (Poales: Poaceae). J. Integr. Pest Manag. 2021, 12, 20. [Google Scholar] [CrossRef]
  24. Iqbal, Z.; Sattar, M.N.; Naqqash, M.N. Diversity and Management of Plant Viruses Infecting Rice. In Modern Techniques of Rice Crop Production; Springer: Berlin/Heidelberg, Germany, 2022. [Google Scholar] [CrossRef]
  25. Dietzgen, R.G.; Bejerman, N.E.; Goodin, M.M.; Higgins, C.M.; Huot, O.B.; Kondo, H.; Martin, K.M.; Whitfield, A.E. Diversity and epidemiology of plant rhabdoviruses. Virus Res. 2020, 281, 197942. [Google Scholar] [CrossRef]
  26. Benjamin, J.; Idowu, O.; Babalola, O.K.; Oziegbe, E.V.; Oyedokun, D.O.; Akinyemi, A.M.; Adebayo, A. Cereal production in Africa: The threat of certain pests and weeds in a changing climate—A review. Agric. Food Secur. 2024, 13, 18. [Google Scholar] [CrossRef]
  27. Balasubramanian, V.; Sie, M.; Hijmans, R.J.; Otsuka, K. Increasing Rice Production in Sub-Saharan Africa: Challenges and Opportunities. Adv. Agron. 2007, 94, 55–133. [Google Scholar] [CrossRef]
  28. Joda, A.O.; Ewete, F.K.; Singh, B.N.; Pitan, O.O. Varietal Differences in Rice (Oryza sativa L.) Resistance to the Shield Bug, Aspavia armigera (Fabricius) (Hemiptera: Pentatomidae). J. Agric. Sci. 2015, 7, 211. [Google Scholar] [CrossRef]
  29. Heinrichs, E.A.; Barrion, A.T. Rice-Feeding Insects and Selected Natural Enemies in West Africa. Biology, Ecology, Identification; IRRI/WARDA: Los Baños, Philippines; Abidjan, Côte d’Ivoire, 2004; p. 243. [Google Scholar]
  30. Polaszek, A.; Fitton, M.G.; Bianchi, G.; Huddleston, T. The parasitoids of the African white rice borer, Maliarpha separatella Ragonot (Lepidoptera: Pyralidae). Bull. Entomol. Res. 1994, 84, 65–89. [Google Scholar] [CrossRef]
  31. Stout, M.; Hadi, B. Rice insect pests: Biology and ecology. In Achieving Sustainable Cultivation of Rice; Burleigh Dodds Science Publishing: Cambridge, UK, 2017; Volume 2, pp. 267–302. [Google Scholar]
  32. Nwilene, F.E.; Nacro, S.; Tamò, M.; Menozzi, P.; Heinrichs, E.A.; Hamadoun, A.; Dakouo, D.; Adda, C.; Togola, A. Managing insect pests of rice in Africa. In Realizing Africa’s Rice Promise; Wopereis, M.C.S., Johnson, D.E., Ahmadi, N., Tollens, E., Jalloh, A., Eds.; CABI: Wallingford, UK, 2013; Chapter 18; pp. 229–240. [Google Scholar]
  33. Bocco, R.; Gandonou, C.B.; Amoussou, P.-L.; Abou, T.; Ibnou, D.; Ndjiondjop, M.N.; Abdoulaye, P.S.; Tamo, M. Rapid phenotyping for identification of rice resistant varieties to Diopsis apicalis (Diptera: Diopsidae) Westwood. Cogent Biol. 2019, 5, 1649851. [Google Scholar] [CrossRef]
  34. Boua, M.; Coulibaly-Ouattara, Y.; Goebel, F.R. Outbreaks of the African sugarcane stalk borer Eldana saccharina Walker (Lepidoptera: Pyralidae) in sugarcane plantations of the northern Ivory Coast: Management strategies under implementation. Pak. Sugar J. 2020, 35, 880–890. [Google Scholar]
  35. Malinga, L. A Novel Approach to the Sterile Insect Technique (SIT) for Eldana saccharina Management in South Africa. Sugar Technol. 2024, 26, 629–634. [Google Scholar] [CrossRef]
  36. Heinrichs, E.A.; Muniappan, R.M. IPM for Tropical Crops: Rice; CABI Reviews: Egham, UK, 2017; pp. 1–31. [Google Scholar]
  37. van Achterberg, C.; Polaszek, A. The parasites of cereal stem borers (Lepidoptera: Cossidae, Crambidae, Noctuidae, Pyralidae) in Africa, belonging to the family Braconidae (Hymenoptera: Ichneumonoidea). Zool. Verh. 1996, 304, 1–123. [Google Scholar]
  38. Togola, A.; Boukar, O.; Tamo, M.; Chamarthi, S. Stem borers of cereal crops in Africa and their management. In Pests Control and Acarology; BoD–Books on Demand: Norderstedt, Germany, 2020; Volume 59. [Google Scholar]
  39. Horgan, F.G. The structure of rice stemborer assemblages: A review of species’ distributions, host ranges, and interspecific interactions. Insects 2023, 14, 921. [Google Scholar] [CrossRef] [PubMed]
  40. Cherry, A.J.; Lomer, C.J.; Djegui, D.; Schulthess, F. Pathogen incidence and their potential as microbial control agents in IPM of maize stem borers in West Africa. BioControl 1999, 44, 301–327. [Google Scholar] [CrossRef]
  41. Nwilene, F.E.; Sanyang, S.; Traore, A.K.; Togola, A.; Goergen, G.; Agunbiade, T.A. Rice Stem Borers: Biology, Ecology and Control—Field Guide and Technical Manual; WARDA: Cotonou, Benin, 2008; p. 28. [Google Scholar]
  42. Meijerman, L.; Ulenberg, S.A. Identification of African stemborer larvae (Lepidoptera: Noctuidae, Pyralidae) based on morphology. Bull. Entomol. Res. 1996, 86, 567–578. [Google Scholar] [CrossRef]
  43. Abdel-Rahman, E.M.; Kimathi, E.; Tawona, M.B.; Tonnang, H.E.Z.; Mongare, R.; Niassy, S.; Subramanian, E. Computational biogeographic distribution of the fall armyworm (Spodoptera frugiperda J.E. Smith) moth in eastern Africa. Heliyon 2023, 9, e16144. [Google Scholar] [CrossRef]
  44. Brévault, T.; Ndiaye, A.; Badiane, D.; Bal, A.B.; Sembène, M.; Silvie, P.; Haran, J. First records of the fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae), in Senegal. Entomol. Gen. 2018, 37, 129–142. [Google Scholar] [CrossRef]
  45. Njuguna, E.; Nethononda, P.; Maredia, K.; Mbabazi, R.; Kachapulula, P.; Rowe, A.; Ndolo, D. Experiences and perspectives on spodoptera frugiperda (Lepidoptera: Noctuidae) management in Sub-Saharan Africa. J. Integr. Pest Manag. 2021, 12, 7. [Google Scholar] [CrossRef]
  46. Gianessi, L.P. The increasing importance of herbicides in worldwide crop production. Pest Manag. Sci. 2013, 69, 1099–1105. [Google Scholar] [CrossRef]
  47. Paramasiva, I.; Rajasekhar, P.; Harathi, P.N.; Vineetha, U. Incidence of insect pests of rice as affected by organic and inorganic fertilizers. J. Entomol. Zool. Stud. 2020, 8, 638–641. [Google Scholar]
  48. Mlambo, S.; Mubayiwa, M.; Tarusikirwa, V.L.; Machekano, H.; Mvumi, B.M.; Nyamukondiwa, C. The fall armyworm and larger grain borer Pest invasions in Africa: Drivers, impacts and implications for food systems. Biology 2024, 13, 160. [Google Scholar] [CrossRef]
  49. Soul-kifouly, G.M. Economics of Biological Control of Cereal Stemborers in Eastern Africa: A Case Study of Maize and Sorghum Production in Kenya. Ph.D. Thesis, Kenyatta University, Kahawa, Kenya, 2018. [Google Scholar]
  50. Baidhe, E.; Clementson, C.L.; Senyah, J.; Hammed, A. Appraisal of Post-Harvest Drying and Storage Operations in Africa: Perspectives on Enhancing Grain Quality. AgriEngineering 2024, 6, 3030–3057. [Google Scholar] [CrossRef]
  51. Tadesse, M. Post-harvest loss of stored grain, its causes and reduction strategies. Food Sci. Qual. Manag. 2020, 96, 26–35. [Google Scholar]
  52. Ogah, E.O.; Nwilene, F.E. Biological control of African rice gall midge (Orseolia oryzivora, Harris and Gagné) in Nigeria: A review. Annu. Res. Rev. Biol. 2014, 4, 2995–3006. [Google Scholar] [CrossRef]
  53. Von, F.A.; Annor-Frempong, F.; Obeng-Mensah, A.; Omega, S. Climate Change Effects, Multi-Actor Interactions, and Effectiveness of Adaptation Activities on Rice Production in Ghana’s Northern Region. J. Advocacy Res. Educ. 2024, 11, 234–243. [Google Scholar]
  54. January, B.; Rwegasira, G.M.; Tefera, T. Rice stem borer species in Tanzania: A review. J. Basic Appl. Zool. 2020, 81, 36. [Google Scholar] [CrossRef]
  55. Benfica, R.; Davis, K.; Oulu, M.; Termote, T.; Fadda, C. The True Costs of Food Production in Kenya and Viet Nam; International Food Policy Research Institute: Washington, DC, USA, 2024. [Google Scholar]
  56. Togola, A.; Seck, P.A.; Glitho, I.A.; Diagne, A.; Adda, C.; Toure, A.; Nwilene, F.E. Economic losses from insect pest infestation on rice stored on-farm in Benin. Unpubl. Rep. 2013, 13, 278–285. [Google Scholar] [CrossRef]
  57. Botha, A.M.; Kunert, K.J.; Maling’a, J.; Foyer, C.H. Defining biotechnological solutions for insect control in Sub-Saharan Africa. Food Energy Secur. 2020, 9, e191. [Google Scholar] [CrossRef]
  58. Faheem, M.; Saeed, S.; Sajjad, A.; Wang, S.; Ali, A. Spatio-temporal variations in wheat aphid populations and their natural enemies in four agro-ecological zones of Pakistan. PLoS ONE 2019, 14, e0222635. [Google Scholar] [CrossRef] [PubMed]
  59. Dunand, R.; Saichuk, J. Rice growth and development. In Louisiana Rice Production Handbook Pub 2321; Louisiana State University: Baton Rouge, LA, USA, 2014; p. 14. [Google Scholar]
  60. Gibicsár, S.; Keszthelyi, S. Topographical based significance of sap-sucking Heteropteran in European wheat cultivations: A systematic review. Diversity 2023, 15, 109. [Google Scholar] [CrossRef]
  61. Paul, A.V. Insect pests and their management. Agriculture. 2008. Available online: https://api.semanticscholar.org/CorpusID:82699925 (accessed on 12 January 2025).
  62. Dey, S. Stem borers, an important yield reducing insect pest complex of rice in India: A review. J. Entomol. Zool. Stud. 2020, 8, 786–789. [Google Scholar]
  63. Narayan, S. Impact analysis of stem borer on rice. J. Entomol. Zool. Stud. 2018, 6, 212–215. [Google Scholar]
  64. Dutta, S.; Roy, N. Review on bionomics and management of rice stem borer. J. Entomol. Zool. Stud. 2022, 10, 301–310. [Google Scholar] [CrossRef]
  65. Rahman, M.T.; Khalequzzaman, M.; Khan, M.A.R. Assessment of infestation and yield loss by stem borers on variety of rice. J. Asia-Pac. Entomol. 2004, 7, 89–95. [Google Scholar] [CrossRef]
  66. Soren, A.; Prasad, R. Management of Rice HISPA (Dicladispa armigera) through use of neem and karanj cake as organic manures. Int. J. Curr. Microbiol. Appl. Sci. 2018, 7, 2911–2916. [Google Scholar]
  67. Chakraborty, K.; Deb, D.C. Incidence of rice hispa, Dicladispa armigera on kharif paddy in northern West Bengal, India. Glob. J. Sci. Front. Res. Biol. Sci. 2012, 12, 52–61. [Google Scholar]
  68. Bhattacharjee, P.P.; Ray, C.D. Effect of season on the development of rice hispa, Dicladispa armigera in Barak Valley of Assam. Trop. Ecol. 2017, 58, 199–203. [Google Scholar]
  69. Mitku, G. Yield Loss Quantification Due to Stalk-Eyed Fly (Diopsidae) Infestations on Rice Crops (Oryza sativa) in Fogera Plain. Middle East Res. J. Agric. Food Sci. 2024, 4, 179–185. [Google Scholar] [CrossRef]
  70. Bocco, R.; Gandonou, C.B.; Elie, D.A.; Séraphin, Z.A. Diopsids (Diopsis thoracica and D. apicalis) damaging rice production in Africa: A review. Int. J. Curr. Res. Biosci. Plant Biol. 2017, 4, 33–41. [Google Scholar] [CrossRef]
  71. Li, A.-M.; Chen, Z.-L.; Liao, F.; Zhao, Y.; Qin, C.-X.; Wang, M.; Pan, Y.-Q.; Wei, S.-L.; Huang, D.-L. Sugarcane borers: Species, distribution, damage and management options. J. Pest Sci. 2024, 97, 1171–1201. [Google Scholar] [CrossRef]
  72. Goebel, F.R.; Way, M.J. Crop Losses Due to Two Sugarcane Stem Borers in Réunion and South Africa; ISSCT: Réduit, Mauritius, 2007. [Google Scholar]
  73. Kale, S.; Mandawi, N.C.; Sahu, H. Seasonal incidence and correlation studies between the rice whorl maggot (Hydrellia philippina) and weather parameters under Bastar Plateau conditions. Int. J. Adv. Biochem. Res. 2023, 7, 250–253. [Google Scholar] [CrossRef]
  74. Litsinger, J.A.; Bandong, J.P.; Canapi, B.L.; Dela Cruz, C.G.; Pantua, P.C.; Alviola, A.L.; Batay-An, E.H., III. Evaluation of action thresholds for chronic rice insect pests in the Philippines: II. Whorl maggot and defoliators. Int. J. Pest Manag. 2006, 52, 167–180. [Google Scholar] [CrossRef]
  75. Kega, V.M.; Olubayo, F.; Kasina, M.; Nderitu, J.H. Assessment of yield loss caused by the African white rice stem borer (Maliarpha separatella Ragonot) at Mwea irrigation scheme, Kirinyaga county, Kenya. J. Entomol. 2016, 13, 19–25. [Google Scholar] [CrossRef]
  76. Heinrichs, E.A.; Adesina, A.A. Contribution of multiple-pest resistance to tropical crop production. In Economic, Environmental, and Social Benefits of Resistance in Field Crops; Entomological Society of America: Annapolis, MD, USA, 1999; p. 149. [Google Scholar] [CrossRef]
  77. Singh, S.K.; Mathur, Y.K.; Yadav, D.K. Study on Mythimna separata to establish Economic threshold level in Rice. Ann. Plant Prot. Sci. 2009, 17, 357–361. [Google Scholar]
  78. Pan, Q.; Shen, J.; Su, L.; Nie, Z.; Shikano, I.; Liu, T.X.; Chen, L. Fitness of Mythimna separata (Lepidoptera: Noctuidae) on Cultivated Wheat and a Weed, Wild Oat (Avena fatua), and Its Implications for Pest Management. Biology 2024, 13, 1037. [Google Scholar] [CrossRef]
  79. Yadav, M.; Prasad, R.; Kumar, P.; Pandey, C.; Prasad, D.; Kumar, P. Effect of date of transplanting on the incidence of green leaf hopper (Nephotettix virescens & N. nigropictus) in rice field, Jharkhand. J. Pharmacogn. Phytochem. 2018, 7, 897–900. [Google Scholar]
  80. Vidya Madhuri, E.; Rupali, J.S.; Sujatha, G.S.; Sharan, S.P.; Saicharan, D. Biochemical changes in rice plants infested by green leafhopper, Nephotettix virescens. Int. J. Adv. Biochem. Res. 2024, 8, 1306–1309. [Google Scholar] [CrossRef]
  81. Srivastava, A.; Pusuluri, M.; Balakrishnan, D.; Vattikuti, J.L.; Neelamraju, S.; Sundaram, R.M.; Mangrauthia, S.K.; Ram, T. Identification and Functional Characterization of Two Major Loci Associated with Resistance against Brown Planthoppers (Nilaparvata lugens) Derived from Oryza nivara. Genes 2023, 14, 2066. [Google Scholar] [CrossRef]
  82. Jeevanandham, N.; Raman, R.; Ramaiah, D.; Senthilvel, V.; Mookaiah, S.; Jegadeesan, R. Rice–Nilaparvata lugens interaction—Current status and future prospects of brown planthopper management. J. Plant Dis. Prot. 2023, 130, 125–141. [Google Scholar] [CrossRef]
  83. Chander, S.; Palta, R.K. Rice brown planthopper, Nilaparvata lugens outbreak in relation to weather factors. Indian J. Entomol. 2010, 72, 178–180. [Google Scholar]
  84. Sama, K.; Nacro, S.; Thiaw, C.; Dakouo, D. Incidence of the African Rice Gall Midge (Orseolia oryzivora) in relation with period of rice transplanting in the Kou Valley, Burkina Faso. Adv. Entomol. 2016, 4, 97. [Google Scholar] [CrossRef]
  85. Nwilene, F.E.; Adeoti, A.O.; Shaibu, A.A. Efficacy of Metarhizium anisopliae and Beauveria bassiana as biological control agents of African Rice Gall Midge (Orseolia oryzivora). In International Journal of Pest Management; Taylor & Francis: Abingdon, UK, 2023. [Google Scholar] [CrossRef]
  86. Baladhiya, H.C.; Sisodiya, D.B.; Pathan, N.P. A review on pink stem borer, Sesamia inferens Walker: A threat to cereals. J. Entomol. Zool. Stud. 2018, 6, 1235–1239. [Google Scholar]
  87. Singh, D.P.; Tiwari, T. Assessment of extent of damage and yield loss caused by stem borer in rice. J. Pharmacogn. Phytochem. 2019, 8, 2112–2115. [Google Scholar]
  88. Esfandiari, M.; Mossadegh, M.S.; Shishehbor, P. Sesamia botanephaga Tams & Bowden, 1953 auct. in Iran, read Sesamia nonagrioides (Lefebvre, 1827) (Lepidoptera: Noctuidae). Munis Entomol. Zool. 2011, 6, 400–403. [Google Scholar]
  89. Pallavi, D.; Sharanabasappa, G.G. Crop loss estimation of yellow stem borer Scirpophaga incertulas (Walker) damage on paddy. J. Entomol. Zool. Stud. 2017, 5, 635–638. [Google Scholar]
  90. Singh, S.; Singh, B.K. Yield loss assessment due to infestation of Scirpophaga incertulas of BPT 5204 rice variety in Patna district of Bihar, India. Int. J. Fauna Biol. Stud. 2020, 7, 125–128. [Google Scholar]
  91. Pantoja, A.; Smith, C.M.; Robinson, J.F. Effects of the Fall Armyworm (Lepidoptera: Noctuidae) on Rice Yields. J. Econ. Entomol. 1986, 79, 1324–1329. [Google Scholar] [CrossRef]
  92. Acharya, R.; Malekera, M.J.; Dhungana, S.K.; Sharma, S.R.; Lee, K.Y. Impact of rice and potato host plants is higher on the reproduction than growth of corn strain fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae). Insects 2022, 13, 256. [Google Scholar] [CrossRef]
  93. Suby, S.B.; Soujanya, P.L.; Yadava, P.; Patil, J.; Subaharan, K.; Prasad, G.S.; Rakshit, S. Invasion of fall armyworm (Spodoptera frugiperda) in India. Curr. Sci. 2020, 119, 44–51. [Google Scholar] [CrossRef]
  94. Rahimoon, M.Y.; Rahimoon, S.A. Comparative efficacy of different botanicals for controlling white stem borer, Scirpophaga innotata (Walker) under field conditions. Pure Appl. Biol. 2023, 12, 1532–1540. [Google Scholar] [CrossRef]
  95. Ghoghari, P.D.; Chavadhari, R.L.; Patil, V.A.; Kavad, N.K. Bio-efficacy of insecticides against rice stem borer, Scirpophaga spp. Int. J. Entomol. Res. 2019, 4, 59–65. [Google Scholar]
  96. Rahaman, M.M.; Islam, K.S.; Jahan, M.; Mamun, M.A.A. Relative abundance of stem borer species and natural enemies in rice ecosystem at Madhupur, Tangail, Bangladesh. J. Bangladesh Agric. Univ. 2014, 12, 267–272. [Google Scholar] [CrossRef]
  97. Viswajyothi, K.; Aggarwal, N.; Jindal, J. The biology of Sesamia inferens (Walker) (Lepidoptera: Noctuidae) on maize in the North Western plains of India. Acta Phytopathol. Entomol. Hung. 2019, 54, 69–84. [Google Scholar] [CrossRef]
  98. Ong’amo, G.; Khadioli, N.; Le Ru, B.; Mujica, N.; Carhuapoma, P. Pest Distribution and Risk Atlas for Africa. 2016. Available online: https://cipotato.org/riskatlasforafrica/current-and-potential-distribution-and-abundance-of-pests/ (accessed on 20 January 2025).
  99. Neupane, S.; Pokhrel, S.; Tiwari, S.; Bhandari, G.; Adhikari, P.; Poudel, S. Biology and Morphometrics of Fall armyworm (Spodoptera frugiperda) in Chitwan, Nepal. Int. J. Appl. Biol. 2023, 7. [Google Scholar] [CrossRef]
  100. Mashhoor, K.; Ramesh, N.; Lazar, K.V.; Shanas, S. Phylogenetic Status of Rice Dark Headed Stemborer, Chilo Polychrysus. Int. J. Pharm. Biol. Sci. 2018, 8, 768–772. [Google Scholar]
  101. De La Pava, N.; Sepulveda-Cano, P.A. Biology of black aphid (Aphis craccivora: Aphididae) on cowpea (Vigna unguiculata, Fabaceae). Acta Biológica Colomb. 2015, 20, 93–97. [Google Scholar] [CrossRef]
  102. Williams, C.T.; Harris, K.M.; Ukwungwu, M.N.; Nacro, S.; Dakouo, D.; Nwilene, F.E.; Singh, B.N.; et Okhidievbie, O. African Rice Gall Midge Research Guide; WARDA: Bouaké, Côte d’Ivoire; CABI: Wallingford, UK, 2002; 28p. [Google Scholar]
  103. Mokhtar, A.; Abdullah, S.W.R. Overview of Yellow Rice Stem Borer, Scirpophaga incertulas in Malaysia. Outlooks Pest Manag. 2024, 35, 126–131. [Google Scholar] [CrossRef]
  104. Rathore, S.; Chandola, M.; Raghuvanshi, R.; Kaur, M.; Singh, K.V. Indigenous pest management practices of indian hill farmers: Introspecting their rationale and communication pattern for secure ecosystems. Sustainability 2021, 13, 11608. [Google Scholar] [CrossRef]
  105. Cai, Y.; Zhang, Q.; Huang, H. Research on big data-driven rice crop rotation systems: Optimization strategies and virtual case studies. Adv. Resour. Res. 2024, 4, 681–702. [Google Scholar]
  106. Lella, N.; Jagadeesh, K. Ecological IPM strategies for management of pests of rice. Pharma Innov. J. 2023, 12, 3814–3818. [Google Scholar]
  107. Esuyawkal, D. Population Dynamics, Yield Loss and Management of Major Insect Pests of Rice (Oryza sativa L.) Crop: A Review. Am. J. Entomol. 2025, 9, 6–14. [Google Scholar] [CrossRef]
  108. Hajjar, M.J.; Ahmed, N.; Alhudaib, K.A.; Ullah, H. Integrated insect pest management techniques for rice. Sustainability 2023, 15, 4499. [Google Scholar] [CrossRef]
  109. Duan, H.; Li, Y.; Yuan, Y. A study on the long-term impact of crop rotation on soil health driven by big data. Geogr. Res. Bull. 2024, 3, 348–369. [Google Scholar]
  110. Josephrajkumar, A.; Mani, M.; Anes, K.M.; Mohan, C. Ecological Engineering in Pest Management in Horticultural and Agricultural Crops. In Trends in Horticultural Entomology; Mani, M., Ed.; Springer: Singapore, 2022. [Google Scholar] [CrossRef]
  111. Huss, C.P.; Holmes, K.D.; Blubaugh, C.K. Benefits and risks of intercropping for crop resilience and pest management. J. Econ. Entomol. 2022, 115, 1350–1362. [Google Scholar] [CrossRef]
  112. Agbor, D.T.; Eboh, K.S.; Sama, D.K.; Teche, L.M.; Tanyi, G.T.; Nkongho, R.N. Maize-legume intercropping and botanical piper mitigating effect on pest populations while enhancing the yield of maize. J. Nat. Pestic. Res. 2023, 6, 100060. [Google Scholar] [CrossRef]
  113. Gu, C.; Bastiaans, L.; Anten, N.P.; Makowski, D.; van Der Werf, W. Annual intercropping suppresses weeds: A meta-analysis. Agric. Ecosyst. Environ. 2021, 322, 107658. [Google Scholar] [CrossRef]
  114. Epidi, T.T.; Bassey, A.E.; Zuofa, K. Influence of intercrops on pests’ populations in upland rice (Oryza sativa L.). Afr. J. Environ. Sci. Technol. 2008, 2, 438–441. [Google Scholar]
  115. Himmelstein, J.; Ares, A.; Gallagher, D.; Myers, J. A meta-analysis of intercropping in Africa: Impacts on crop yield, farmer income, and integrated pest management effects. Int. J. Agric. Sustain. 2017, 15, 1–10. [Google Scholar] [CrossRef]
  116. Boudreau, M.A. Diseases in intercropping systems. Annu. Rev. Phytopathol. 2013, 51, 499–519. [Google Scholar] [CrossRef]
  117. Kega, V.M.; Nderitu, J.H.; Kasina, M.; Olubayo, F. Influence of cropping and irrigation systems on population fluctuation of the African white rice stem borer (Maliarpha separatella Rag) and damage on rice. J. Entomol. 2015, 12, 95–102. [Google Scholar] [CrossRef]
  118. Mugisa, I.; Fungo, B.; Kabiri, S.; Sseruwu, G.; Kabanyoro, R. Productivity optimization in rice-based intercropping systems of Central Uganda. Int. J. Environ. Agric. Biotechnol. 2020, 5, 142–149. [Google Scholar] [CrossRef]
  119. Daryanto, S.; Fu, B.; Zhao, W.; Wang, S.; Jacinthe, P.A.; Wang, L. Ecosystem service provision of grain legume and cereal intercropping in Africa. Agric. Syst. 2020, 178, 102761. [Google Scholar] [CrossRef]
  120. Ortiz, J.C.; Ruiz, A.T.; Morales-Ramos, J.A.; Thomas, M.; Rojas, M.G.; Tomberlin, J.K.; Jullien, R.L. Insect mass production technologies. In Insects as Sustainable Food Ingredients; Academic Press: Cambridge, MA, USA, 2016; pp. 153–201. [Google Scholar] [CrossRef]
  121. Raupp, M.J.; Koehler, C.S.; Davidson, J.A. Advances in implementing integrated pest management for woody landscape plants. In Handbook of Integrated Pest Management for Turf and Ornamentals; CRC Press: Boca Raton, FL, USA, 2020; pp. 125–135. [Google Scholar]
  122. Bulut, S.; Arslan, M. Plant protection methods in organic farming. Curr. Trends Nat. Sci. 2023, 12, 183–192. [Google Scholar] [CrossRef]
  123. CARE. Guidelines for Promoting Safer and More Effective Pest Management with Small Holder Farmers: A Contribution to USAID-FFP Environmental Compliance. Prepared for CARE’s FRCT by Sarah Gladstone and Allan Hruska; CARE: Atlanta, GA, USA, 2003. [Google Scholar]
  124. Rodenburg, J.; Johnson, D.E. Weed management in rice-based cropping systems in Africa. Adv. Agron. 2009, 103, 149–218. [Google Scholar]
  125. Mousseau, F. The untold success story of agroecology in Africa. Development 2015, 58, 341–345. [Google Scholar] [CrossRef]
  126. Agyen-Sampong, M.; Prakah-Asante, K.; Fomba, S.N. Rice improvement in the mangrove swamps of West Africa. In Selected Papers of the Dakar Symposium on Acid Sulphate Soils: Dakar, Senegal, January 1986; International Institute for Land Reclamation and Improvement/ILRI: Wageningen, The Netherlands, 1988; p. 163. [Google Scholar]
  127. Dakouo, D.; Bonzi, M.S.; Sawadogo, A.; Dabiré, C.L.; Nacro, S.; Thio, B. Integrated pest management in Burkina Faso. In Integrated Pest Management in the Global Arena; CABI Publishing: Wallingford, UK, 2003; pp. 109–118. [Google Scholar]
  128. Heinrichs, E.A.; Sy, A.A.; Akator, S.K.; Oyediran, I. Seasonal occurrence of rice yellow mottle virus in lowland rice in Côte d’Ivoire. Int. J. Pest Manag. 1997, 43, 291–297. [Google Scholar] [CrossRef]
  129. Getu, E.; Tadesse, A.; Negeri, M.; Tefera, T.; Tsaheye, H.; Dejene, A. Review of entomological research on maize, sorghum and millet. In Increasing Crop Production through Improved Plant Protection; Plant Protection Society of Ethiopia: Addis Ababa, Ethiopia, 2006; Volume 1, p. 167. [Google Scholar]
  130. Showler, A.T.; Reagan, T.E. Mexican rice borer, Eoreuma loftini (Dyar) (Lepidoptera: Crambidae): Range expansion, biology, ecology, control tactics, and new resistance factors in United States sugarcane. Am. Entomol. 2017, 63, 36–51. [Google Scholar] [CrossRef]
  131. Kalaisekar, A.; Padmaja, P.G.; Bhagwat, V.R.; Patil, J.V. Insect Pests of Millets: Systematics, Bionomics, and Management; Academic Press: Cambridge, MA, USA, 2016. [Google Scholar]
  132. Briggs, A.; Pryke, J.S.; Samways, M.J.; Conlong, D.E. Macrophytes promote aquatic insect conservation in artificial ponds. Aquat. Conserv. 2019, 29, 1190–1201. [Google Scholar] [CrossRef]
  133. Ratnadass, A. Trip Report: South Africa, 30 April–7 May 2005; CIRAD-CA: Montpellier, France, 2005. [Google Scholar]
  134. Kalaisekar, A.; Padmaja, P.G. Insect pests of millets and their host plant relations. In Millets and Sorghum: Biology and Genetic Improvement; John Wiley & Sons: Hoboken, NJ, USA, 2017; pp. 267–290. [Google Scholar]
  135. Abrokwah, L.A.; Torkpo, S.K.; Pereira, G.D.S.; Oppong, A.; Eleblu, J.; Pita, J.; Offei, S.K. Rice Yellow Mottle Virus (RYMV): A Review. Viruses 2024, 16, 1707. [Google Scholar] [CrossRef] [PubMed]
  136. Holkar, S.K.; Balasubramaniam, P.; Kumar, A.; Kadirvel, N.; Shingote, P.R.; Chhabra, M.L.; Kumar, S.; Kumar, P.; Viswanathan, R.; Jain, R.K.; et al. Present status and future management strategies for Sugarcane yellow leaf virus: A major constraint to the global sugarcane production. Plant Pathol. J. 2020, 36, 536. [Google Scholar] [CrossRef]
  137. Silvie, P.; Togola, A. Principaux Insectes Ravageurs du riz en Afrique et Méthodes de Lutte Non Chimiques. SupAgro, 15 Février 2013. DES Gembloux-UCL (Master Complémentaire en Protection des Cultures Tropicales et Subtropicales); CIRAD-CA: Montpellier, France, 2013. [Google Scholar]
  138. Maes, K.V.N. Superfamille Pyraloidea: Crambidae, Pyralidae. In Les Foreurs des Tiges de Céréales en Afrique: Importance Économique, Systématique, Ennemis Naturels Et Méthodes de Lutte; Editions Quae: Paris, France, 2000; p. 91. [Google Scholar]
  139. Jeanguenat, A.; Lamberth, C. Sulfur-based functional groups in agrochemistry. Pest Manag. Sci. 2023, 79, 2647–2663. [Google Scholar] [CrossRef]
  140. Rebe, M.; Van den Berg, J.; McGeoch, M.A. Growth and development of Chilo partellus (Swinhoe) (Lepidoptera: Crambidae) on cultivated and indigenous graminaceous host plants. Afr. Entomol. 2004, 12, 253–258. [Google Scholar]
  141. Kergoat, G.J.; Toussaint, E.F.; Capdevielle-Dulac, C.; Clamens, A.L.; Ong’Amo, G.; Conlong, D.; Le Ru, B. Integrative taxonomy reveals six new species related to the Mediterranean corn stalk borer Sesamia nonagrioides (Lefèbvre) (Lepidoptera: Noctuidae: Sesamiina). Zool. J. Linn. Soc. 2015, 175, 244–270. [Google Scholar] [CrossRef]
  142. Hévin, N.M.; Kergoat, G.J.; Zilli, A.; Capdevielle-Dulac, C.; Musyoka, B.K.; Sezonlin, M.; Le Ru, B. Revisiting the taxonomy and molecular systematics of Sesamia stemborers (Lepidoptera: Noctuidae: Apameini: Sesamiina): Updated classification and comparative evaluation of species delimitation methods. Arthropod Syst. Phylogeny 2024, 82, 447–501. [Google Scholar] [CrossRef]
  143. Ouaba, J.; Tchuinkam, T.; Waïmane, A.; Magara, H.J.O.; Niassy, S.; Meutchieye, F. Lepidopterans of economic importance in Cameroon: A systematic review. J. Agric. Food Res. 2022, 8, 100286. [Google Scholar] [CrossRef]
  144. Hussain, S.; Sher, A.; Nawaz, A.; Sarfraz, M.; Ijaz, M.; Ul-Allah, S.; Sattar, A. Agronomic Crops: Volume 1: Production Technologies; Springer Nature: London, UK, 2019; p. 273. [Google Scholar]
  145. Harris, K.M. Lepidopterous stem borers of cereals in Nigeria. Bull. Entomol. Res. 1962, 53, 139–171. [Google Scholar] [CrossRef]
  146. Ndemah, R.; Schulthess, F.; Le Rü, B.; Bame, I. Lepidopteran cereal stemborers and associated natural enemies on maize and wild grass hosts in Cameroon. J. Appl. Entomol. 2007, 131, 658–668. [Google Scholar] [CrossRef]
  147. Ong’amo, G.O.; Ndemah, R.; Le Ru, B.P.; Le Gall, P. Diversity and host range of lepidopteran stemborer species in Cameroon. Afr. Entomol. 2014, 22, 625–635. [Google Scholar] [CrossRef]
  148. Gouin, A.; Bretaudeau, A.; Nam, K.; Gimenez, S.; Aury, J.M.; Duvic, B.; Hilliou, F.; Durand, N.; Montagné, N.; Darboux, I.; et al. Two genomes of highly polyphagous lepidopteran pests (Spodoptera frugiperda, Noctuidae) with different host-plant ranges. Sci. Rep. 2017, 7, 11816. [Google Scholar] [CrossRef]
  149. Agravante, A.S.; Alviar, K.B.; Ramirez, A.H.A.; Yap, S.A. Biology of Spodoptera frugiperda (JE Smith) (Lepidoptera: Noctuidae) on selected weed species associated with corn in North Cotabato, Philippines. Philipp J. Sci. 2022, 151, 2011–2020. [Google Scholar] [CrossRef]
  150. Fang, M.; Lu, S.H.; Yao, L.; Li, G.T.; Zheng, R.W.; Tang, Q.F. Effects of different host-plant components on physiological indices in Spodoptera frugiperda. Interciencia 2022, 47, 335–340. [Google Scholar]
  151. Senanayake, D.M.J.B.; Cooray, W.H.K.; Nayanakantha, N.M.C.; Dhammika, W.A.R.; Sarathchandra, S.R.; Madduma, M.R.A.B.; Dissanayake, D.M.O.K.B.; Dissanayake, D.A.G.; Piyasiri, C.H.; Weerasinghe, E.A.D.N.; et al. Differential Responses of Rathu Heenati Accessions Available in Sri Lanka for Brown Planthopper [Nilaparvata lugens (Stål)] Resistance. Trop. Agric. 2023, 171, 1. [Google Scholar] [CrossRef]
  152. Cheng, X.; Zhou, G.; Chen, W.; Tan, L.; Long, Q.; Cui, F.; Tan, L.; Zou, G.; Tan, Y. Current Status of Molecular Rice Breeding for Durable and Broad-Spectrum Resistance to Major Diseases and Insect Pests. Theor. Appl. Genet. 2024, 137, 219. [Google Scholar] [CrossRef]
  153. Wang, J.; Hu, H.; Jiang, X.; Zhang, S.; Yang, W.; Dong, J.; Yang, T.; Ma, Y.; Zhou, L.; Chen, J.; et al. Pangenome-Wide Association Study and Transcriptome Analysis Reveal a Novel QTL and Candidate Genes Controlling Both Panicle and Leaf Blast Resistance in Rice. Rice 2024, 17, 27. [Google Scholar] [CrossRef]
  154. Li, A.; Zhu, P.; Kong, D.; Wang, L.; Zhang, A.; Liu, Y.; Yu, X.; Luo, L.; Wang, F. Using Marker-Assisted Selection to Develop a Drought-Tolerant Rice Line with Enhanced Resistance to Blast and Brown Planthopper. Agronomy 2024, 14, 2566. [Google Scholar] [CrossRef]
  155. Deng, Z.; Qin, P.; Liu, K.; Jiang, N.; Yan, T.; Zhang, X.; Fu, C.; He, G.; Wang, K.; Yang, Y. The Development of Multi-Resistant Rice Restorer Lines and Hybrid Varieties by Pyramiding Resistance Genes against Blast and Brown Planthopper. Agronomy 2024, 14, 878. [Google Scholar] [CrossRef]
  156. Danso Ofori, A.; Zheng, T.; Titriku, J.K.; Appiah, C.; Xiang, X.; Kandhro, A.G.; Ahmed, M.; Zheng, A. The Role of Genetic Resistance in Rice Disease Management. Int. J. Mol. Sci. 2025, 26, 956. [Google Scholar] [CrossRef]
  157. Williams, C.T.; Ukwungwu, M.N.; Singh, B.N.; Okhidievbie, O.; Nnabo, J. Farmer-Managed Trials in South-East Nigeria to Evaluate the Rice Variety Cisadane and Estimate Yield Losses Caused by the African Rice Gall Midge, Orseolia oryzivora Harris & Gagné. Int. J. Pest Manag. 1999, 45, 117–124. [Google Scholar] [CrossRef]
  158. Mutiga, S.K.; Rotich, F.; Were, V.M.; Kimani, J.M.; Mwongera, D.T.; Mgonja, E.; Onaga, G.; Konaté, K.; Razanaboahirana, C.; Bigirimana, J.; et al. Integrated Strategies for Durable Rice Blast Resistance in Sub-Saharan Africa. Plant Dis. 2021, 105, 2749–2770. [Google Scholar] [CrossRef] [PubMed]
  159. Eriksson, D.; Akoroda, M.; Azmach, G.; Labuschagne, M.; Mahungu, N.; Ortiz, R. Measuring the Impact of Plant Breeding on Sub-Saharan African Staple Crops. Outlook Agric. 2018, 47, 163–180. [Google Scholar] [CrossRef]
  160. Sharma, H.C.; Dhillon, M.K.; Manchanda, P.; Taggar, G.K.; Sarao, P.S. Molecular Markers for Insect Resistance: Potential and Limitations. In Molecular Advances in Insect Resistance of Field Crops: Modern and Applied Approaches; Springer: Cham, Switzerland, 2022; pp. 87–116. [Google Scholar]
  161. Pathak, M.; Saxena, R. Insect Resistance in Crop Plants. Comment. Plant Sci. 2013, 2, 61. [Google Scholar]
  162. Patitungkho, S.; Laead-On, K.; Patitungkho, K. Biological Investigation of Nano-Organometallic Agents Against Bacteria and Chilo polychrysus. J. Agric. Chem. Environ. 2023, 12, 238–249. [Google Scholar] [CrossRef]
  163. Chaudhary, R.C.; Khush, G.S. Breeding Rice Varieties for Resistance Against Chilo spp. of Stem Borers in Asia and Africa. Int. J. Trop. Insect Sci. 1990, 11, 659–669. [Google Scholar] [CrossRef]
  164. Ma, M.; Wu, S.; Peng, Z.; Li, K. Resistance Monitoring of Chilo suppressalis (Lepidoptera: Crambidae) to Chlorantraniliprole in Five Field Populations from Hunan, China 2013–2020. J. Entomol. Sci. 2024, 59, 49–59. [Google Scholar] [CrossRef]
  165. Wang, Y.; Ju, D.; Yang, X.; Ma, D.; Wang, X. Comparative Transcriptome Analysis Between Resistant and Susceptible Rice Cultivars Responding to Striped Stem Borer (Chilo suppressalis) Infestation. Front. Physiol. 2018, 9, 1717. [Google Scholar] [CrossRef]
  166. Srivastava, A.; Tandon, V. Screening of Rice Genotypes Against Rice Hispa Dicladispa armigera Olivier. Indian J. Entomol. 2020, 82, 678–680. [Google Scholar] [CrossRef]
  167. Mankotia, B.S.; Sharma, P.K.; Shekhar, J.; Sood, G.K.; Thakur, R.C. Upland Rice in Himachal Pradesh. In Upland Rice in India; Scientific Publishers: Berlin, Germany, 2011; p. 107. [Google Scholar]
  168. Weelar, C.G.; Lamo, J.; Otim, M.H.; Awio, B.; Ochwo-Ssemakula, M. Mode of Inheritance of Resistance to the Stalk-Eyed Fly (Diopsis longicornis) in Rice. Int. J. Agron. Agri. R. 2017, 10, 9–20. [Google Scholar]
  169. Togola, A.; Nwilene, F.E.; Agbaka, A.; Degila, F.; Tolulope, A.; Chougourou, D. Screening Upland Varieties of NERICA and Its Parents for Resistance to Stalk-Eyed Fly, Diopsis sp. (Diptera, Diopsidae) in Benin. J. Appl. Sci. 2011, 11, 145–150. [Google Scholar] [CrossRef]
  170. Weelar, C.G.; Otim, M.H.; Lamo, J.; Awio, B.; Ochwo-Ssemakula, M. Evaluation of Rice Genotypes for Resistance to the Stalk-Eyed Fly (Diopsis longicornis) in Rice in Uganda. Int. J. Agron. Agric. Res. 2016, 9, 9–21. [Google Scholar]
  171. Keeping, M.G.; Rutherford, R.S. Resistance Mechanisms of South African Sugarcane to the Stalk Borer Eldana saccharina (Lepidoptera: Pyralidae): A Review. Proc. S. Afr. Sug. Technol. Ass. 2004, 78, 307–312. [Google Scholar]
  172. Mahlanza, T.; Rutherford, R.S.; Snyman, S.J.; Watt, M.P. Eldana saccharina (Lepidoptera: Pyralidae) Resistance in Sugarcane (Saccharum sp.): Effects of Fusarium spp., Stalk Rind, Fibre and Nitrogen Content. Afr. Entomol. 2014, 22, 810–822. [Google Scholar] [CrossRef]
  173. Kumar, N.; Sah, S.B.; Gupta, R.N.; Kumar, R. Evaluation of Rice Genotypes Against Rice Leaf Folder, Cnaphalocrocis medinalis Guenee in Koshi Region of Bihar. Ann. Plant Prot. Sci. 2023, 31, 75–80. [Google Scholar] [CrossRef]
  174. Pradhan, S.K.; Behera, L.; Barik, S.R.; Sanghamitra, P.; Anandan, A.; Sah, R.P.; Meher, J. High Yielding Varieties for Increasing Rice Production of Rainfed Shallow Lowlands in Eastern India. Indian Farming 2021, 71, 4. [Google Scholar]
  175. Jackson, G. Pacific Pests & Pathogens—Full Size Fact Sheets. 2021. Available online: https://apps.lucidcentral.org/ppp/text/web_full/entities/index.htm (accessed on 12 January 2025).
  176. Mandal, N.P.; Maiti, D.; Roy, S.; Banerjee, A.; Singh, C.V.; Variar, M. Rainfed Upland Rice: Activities, Achievements and Aspirations. In National Rice Research Institute: Activities, Achievements and Aspirations; ICAR-National Rice Research Institute: Cuttack, India, 2019; p. 190. [Google Scholar]
  177. Litsinger, J.A.; Canapi, B.L.; Bandong, J.P.; Lumaban, M.D.; Raymundo, F.D.; Barrion, A.T. Insect Pests of Rainfed Wetland Rice in the Philippines: Population Densities, Yield Loss, and Insecticide Management. Int. J. Pest Manag. 2009, 55, 221–242. [Google Scholar] [CrossRef]
  178. Kega, V.M.; Kasina, M.; Olubayo, F.; Nderitu, J.H. Management of Maliarpha separatella Rag Using Effective Entomopathogenic Nematodes and Resistant Rice Cultivars. J. Entomol. 2013, 10, 103–109. [Google Scholar] [CrossRef]
  179. Malinga, Y.W.K. The Performance of Selected Rice Varieties for Relative Resistance to Stem-Borer, Maliarpha separatella (Rag.), Attack Under Field Conditions. Int. J. Trop. Insect Sci. 1985, 6, 227–231. [Google Scholar] [CrossRef]
  180. Mishra, A.; Barik, S.R.; Pandit, E.; Yadav, S.S.; Das, S.R.; Pradhan, S.K. Genetics, Mechanisms and Deployment of Brown Planthopper Resistance Genes in Rice. Crit. Rev. Plant Sci. 2022, 41, 91–127. [Google Scholar] [CrossRef]
  181. Padmakumari, A.P.; Kota, S.; Sundaram, R.M. Current Status of Host Plant Resistance to Insects in Rice and Future Perspectives. In Plant Resistance to Insects in Major Field Crops; Springer Nature: Singapore, 2024; pp. 69–122. [Google Scholar]
  182. Du, B.; Chen, R.; Guo, J.; He, G. Current Understanding of the Genomic, Genetic, and Molecular Control of Insect Resistance in Rice. Mol. Breed. 2020, 40, 24. [Google Scholar] [CrossRef]
  183. Kakde, A.M.; Patel, K.G. Varietal Screening of Rice Against Green Leaf Hopper, Nephotettix virescens Distal. Int. J. Plant Prot. 2018, 11, 46–50. [Google Scholar] [CrossRef]
  184. Wan, P.J.; Zhou, R.N.; Nanda, S.; He, J.C.; Yuan, S.Y.; Wang, W.X.; Lai, F.X.; Fu, Q. Phenotypic and Transcriptomic Responses of Two Nilaparvata lugens Populations to the Mudgo Rice Containing Bph1. Sci. Rep. 2019, 9, 14049. [Google Scholar] [CrossRef]
  185. Kumar, K.; Kaur, P.; Kishore, A.; Vikal, Y.; Singh, K.; Neelam, K. Recent Advances in Genomics-Assisted Breeding of Brown Planthopper (Nilaparvata lugens) Resistance in Rice (Oryza sativa). Plant Breed. 2020, 139, 1052–1066. [Google Scholar] [CrossRef]
  186. Shi, S.; Wang, H.; Zha, W.; Wu, Y.; Liu, K.; Xu, D.; He, G.; Zhou, L.; You, A. Recent Advances in the Genetic and Biochemical Mechanisms of Rice Resistance to Brown Planthoppers (Nilaparvata lugens Stål). Int. J. Mol. Sci. 2023, 24, 16959. [Google Scholar] [CrossRef]
  187. Ekka, R.E.; Sarawgi, A.K.; Kanwar, R.R. Genetics of Brown Plant Hopper (Nilaparvata lugens Stål.) Resistance in Elite Donors of Rice (Oryza sativa L.). J. Pharmacogn. Phytochem. 2019, 8, 1187–1191. [Google Scholar]
  188. Kiswanto, I.; Soetopo, L.; Adiredjo, A.L. Identification of Novel Candidate of Brown Planthopper Resistance Gene Bph44 in Rice (Oryza sativa L.). Genome 2022, 65, 505–511. [Google Scholar] [CrossRef]
  189. Muduli, L.; Pradhan, S.K.; Mishra, A.; Bastia, D.N.; Samal, K.C.; Agrawal, P.K.; Dash, M. Understanding Brown Planthopper Resistance in Rice: Genetics, Biochemical and Molecular Breeding Approaches. Rice Sci. 2021, 28, 532–546. [Google Scholar] [CrossRef]
  190. Ji, H.; Kim, S.R.; Kim, Y.H.; Suh, J.P.; Park, H.M.; Sreenivasulu, N.; Misra, G.; Kim, S.M.; Hechanova, S.L.; Kim, H.; et al. Map-Based Cloning and Characterization of the BPH18 Gene from Wild Rice Conferring Resistance to Brown Planthopper (BPH) Insect Pest. Sci. Rep. 2016, 6, 34376. [Google Scholar] [CrossRef]
  191. Horgan, F.G.; Ramal, A.F.; Bentur, J.S.; Kumar, R.; Bhanu, K.V.; Sarao, P.S.; Iswanto, E.H.; Chien, H.V.; Phyu, M.H.; Bernal, C.C.; et al. Virulence of Brown Planthopper (Nilaparvata lugens) Populations from South and South East Asia Against Resistant Rice Varieties. Crop Prot. 2015, 78, 222–231. [Google Scholar] [CrossRef]
  192. Heinrichs, E.A.; Pathak, P.K. Resistance to the Rice Gall Midge, Orseolia oryzae, in Rice. Int. J. Trop. Insect Sci. 1980, 1, 123–132. [Google Scholar] [CrossRef]
  193. Yao, N.; Lee, C.R.; Semagn, K.; Sow, M.; Nwilene, F.; Kolade, O.; Bocco, R.; Oyetunji, O.; Mitchell-Olds, T.; Ndjiondjop, M.N. QTL Mapping in Three Rice Populations Uncovers Major Genomic Regions Associated with African Rice Gall Midge Resistance. PLoS ONE 2016, 11, e0160749. [Google Scholar] [CrossRef]
  194. Jeevanandham, N.; Ramiah, N.; Chockalingam, V.; Jegadeesan, R. An Overview of the Bionomics, Host Plant Resistance and Molecular Perspectives of Sesamia inferens Walker in Cereals and Millets. Agronomy 2020, 10, 1705. [Google Scholar] [CrossRef]
  195. Ajala, S.O.; Aroga, R.; Odiyi, A.; Olaoye, G. Screening and Breeding for Resistance to Maize Stem Borers and Eldana in West and Central Africa. Afr. Crop Sci. Conf. Proc. 2009, 9, 559–564. [Google Scholar]
  196. Liu, Z.; Gao, Y.; Luo, J.; Lai, F.; Li, Y.; Fu, Q.; Peng, Y. Evaluating the Non-Rice Host Plant Species of Sesamia inferens (Lepidoptera: Noctuidae) as Natural Refuges: Resistance Management of Bt Rice. Environ. Entomol. 2011, 40, 749–754. [Google Scholar] [CrossRef] [PubMed]
  197. Soujanya, P.L.; Sekhar, J.C.; Karjagi, C.G.; Ratnavathi, C.V.; Venkateswarlu, R.; Yathish, K.R.; Suby, S.B.; Sunil, N.; Rakshit, S. Role of Morphological Traits and Cell Wall Components in Imparting Resistance to Pink Stem Borer, Sesamia inferens Walker in Maize. Front. Plant Sci. 2023, 14, 1167248. [Google Scholar] [CrossRef] [PubMed]
  198. Geerthana, S.; Justin, G.L.; Soundararajan, R.P.; Jeyaprakash, P. Screening of Rice Genotypes and Assessment of Biophysical Characters Conferring Resistance Against Pink Stem Borer, Sesamia inferens Walker (Lepidoptera: Noctuidae). Biol. Forum Int. J. 2022, 14, 1439–1445. [Google Scholar]
  199. Silva, C.L.T.; Correa, F.; Almeida, A.C.S.; Araújo, M.D.S.; Barrigossi, J.A.D.F.; Jesus, F.G.D. Resistance of Rice Genotypes to Fall Armyworm Spodoptera frugiperda (Lepidoptera: Noctuidae). Rev. Bras. Entomol. 2021, 65, e20210020. [Google Scholar]
  200. Haldhar, S.M.; Saha, R.K.; Nagesh, M. Souvenir-Cum-Abstract Book: National Conference on Priorities in Crop Protection for Sustainable Agriculture; Central Agricultural University: Imphal, Mamipur, 2020; pp. 1–282. [Google Scholar]
  201. Joshi, S.; Tiwari, S.N. Screening of Different Rice Germplasms Against Yellow Stem Borer (Scirpophaga incertulas). Pharma Innov. J. 2022, 11, 748–752. [Google Scholar]
  202. Paramasiva, I.; Sreelakshmi, C.; Vineetha, U.; Harathi, P.N.; Rajasekhar, P. Screening of Advanced Rice Cultures Against Stem Borer, Scirpophaga incertulas (Walker) and Leaf Folder, Cnaphalocrocis medinalis (Guenee). J. Entomol. Zool. Stud. 2021, 9, 390–393. [Google Scholar]
  203. Mackill, D.J.; Khush, G.S. IR64: A High-Quality and High-Yielding Mega Variety. Rice 2018, 11, 18. [Google Scholar] [CrossRef]
  204. Natarajan, D.; Ramaswamy, S.; Paramasiwam, J.; Palanisamy, S.R.; Gnanadhas, P.; Malaichamy, K. Ultrastructural and Morpho-Anatomical Features of Rice Plants Confer First-Level of Defense Against Yellow Stem Borer (Scirpophaga incertulas Walker) Infestation. Arthropod-Plant Interact. 2022, 16, 263–273. [Google Scholar] [CrossRef]
  205. Devasena, N.; Soundararajan, R.P.; Reuolin, S.J.; Jeyaprakash, P.; Robin, S. Evaluation of Rice Genotypes for Resistance to Yellow Stem Borer, Scirpophaga incertulas (Walker) Through Artificial Screening Methods. J. Entomol. Zool. Stud. 2018, 6, 874–878. [Google Scholar]
  206. Rajpoot, S.K.S.; Dixit, S.; Prasad, V.; Giri, S.P.; Singh, R.A.; Parkash, N.; Upadhay, A.L.; Chandra, S. Evaluation of Insecticides and Biopesticides Against Scirpophaga incertulas (Walker), Leaf Folder (Cnaphalocrocis medinalis) and Green Leafhopper in Basmati Rice. Pharma Innov. J. 2021, 10, 368–371. [Google Scholar]
  207. Sawant, V.P.; Narangalkar, A.; Varik, G. Efficacy of Chlorpyriphos 75WDG Against Rice Stem Borer, Scirpophaga incertulas Walker (Lepidoptera: Pyralidae). Int. J. Fauna Biol. Stud. 2019, 6, 41–44. [Google Scholar]
  208. Rani, L.; Thapa, K.; Kanojia, N.; Sharma, N.; Singh, S.; Grewal, A.S.; Srivastav, A.L.; Kaushal, J. An Extensive Review on the Consequences of Chemical Pesticides on Human Health and Environment. J. Clean. Prod. 2021, 283, 124657. [Google Scholar] [CrossRef]
  209. Cooper, J.; Dobson, H. The Benefits of Pesticides to Mankind and the Environment. Crop Prot. 2007, 26, 1337–1348. [Google Scholar] [CrossRef]
  210. Matowo, N.S.; Tanner, M.; Munhenga, G.; Mapua, S.A.; Finda, M.; Utzinger, J.; Ngowi, V.; Okumu, F.O. Patterns of pesticide usage in agriculture in rural Tanzania call for integrating agricultural and public health practices in managing insecticide-resistance in malaria vectors. Malar. J. 2020, 19, 257. [Google Scholar] [CrossRef]
  211. Theriault, V.; Jiang, W.; Diarra, A.; Haggblade, S.; Edmund, J.; Ipou Ipou, J.; Traore, A. Qualitative assessment of pesticide risks in West Africa. In FtF Innov. Lab Food Policy Reseach Pap; Michigan State University: East Lansing, MI, USA, 2020; 35p. [Google Scholar]
  212. Nonga, H.E.; Mdegela, R.H.; Lie, E.; Sandvik, M.; Skaare, J.J. Assessment of Farming Practices and Uses of Agrochemicals in Lake Manyara Basin, Tanzania. Afr. J. Agric. Res. 2011, 6, 2216–2230. [Google Scholar]
  213. Dhakal, A.; Poudel, S. Integrated Pest Management (IPM) and Its Application in Rice—A Review. Rev. Food Agric. 2020, 1, 39–43. [Google Scholar] [CrossRef]
  214. Bragg, D.E.; Silvia, I.R.; John, G.; Uma, S.; Abrol, D.P. Integrated Pest Management in Tropical Cereal Crops. In Integrated Pest Management in the Tropics; New India Publishing Agency: New Delhi, India, 2016; pp. 249–273. [Google Scholar]
  215. Yadav, P.K.; Sharma, S.; Sharma, A. Management Trends of Rice Insect Pests in South Asia: A Review. Food Agric. 2021, 2, 46–53. [Google Scholar] [CrossRef]
  216. Gianessi, L. Importance of Pesticides for Growing Wheat in Sub-Saharan Africa. Int. Pestic. Benefits Case Study 2014, 104, 1–4. [Google Scholar]
  217. Horgan, F.G. Revisiting Research and Methods in Stemborer-Rice Interactions for Integration into Future Breeding Programs; CABI Reviews: Egham, UK, 2023. [Google Scholar]
  218. Sallam, M.; Allsopp, P. Preparedness for Borer Incursion: SRDC Final Report BSS249; BSES: New Delhi, India, 2003. [Google Scholar]
  219. Joda, A.O.; Ewete, F.K.; Pitan, O.O.R. Evaluation of some insecticides for the control of Aspavia armigera Fabricius on rice (Oryza sativa Linn.). Moor J. Agric. Res. 2018, 19, 1. [Google Scholar]
  220. Mringi, S.E. The Potential of Field Margin Pesticidal Plants on Bean Production and Ecosystem Services in Arusha, Tanzania. Ph.D. Thesis, NM-AIST, Arusha, Tanzania, 2017. [Google Scholar]
  221. Rutikanga, A. Pesticides Use and Regulations in Rwanda: Status and Potential for Promotion of Biological Control Methods. Master’s Thesis, Université de Neuchâtel, Faculty of Science, Neuchâtel, Switzerland, 2015. [Google Scholar]
  222. Wu, J.; Ge, L.; Liu, F.; Song, Q.; Stanley, D. Pesticide-induced planthopper population resurgence in rice cropping systems. Annu. Rev. Entomol. 2020, 65, 409–429. [Google Scholar] [CrossRef] [PubMed]
  223. Badu-Apraku, B.; Fakorede, M.A.B. Breeding Maize for Insect Pest Resistance. In Advances in Genetic Enhancement of Early and Extra-Early Maize for Sub-Saharan Africa; Springer: Berlin/Heidelberg, Germany, 2017; pp. 411–425. [Google Scholar]
  224. Otim, M.H.; Alibu, S.; Asea, G.; Abalo, G.; Sserumaga, J.P.; Adumo, S.; Alupo, J.; Ochen, S.; Tefera, T.; Bruce, A.Y.; et al. Performance of Bt Maize Event MON810 in Controlling Maize Stem Borers Chilo partellus and Busseola fusca in Uganda. Crop Prot. 2022, 156, 105945. [Google Scholar] [CrossRef]
  225. Gambari, L.I.; Babatunde, S.F.; John, O.A.; Akor, R.U.; Ogbaje, S.O.; Ajuu, S.N.; Tyoapine, T.S. Effects of Azadirachta indica, Parkia biglobosa and Synthetic Insecticides on Sesamia calamistis (Hampson) on Growth and Yield of Maize (Zea mays L.) in Makurdi. FUDMA J. Sci. 2023, 7, 234–239. [Google Scholar] [CrossRef]
  226. Leslie, G.W.; Moodley, S. A Preliminary Assessment of New Insecticides for the Control of the Sugarcane Borer Eldana saccharina Walker (Lepidoptera: Pyralidae). In Proceedings of the 87th Annual Congress of the South African Sugar Technologists’ Association, Pietermaritzburg, South Africa, 20–22 August 2014. [Google Scholar]
  227. Achadian, E.M.; Goebel, F.R.; Nikpay, A. Current and Future Actions for Integrated Management of Sugarcane Stem Borers in Indonesia: A Case Study of Chilo sacchariphagus (Bojer) (Lepidoptera: Crambidae). Proc. Int. Soc. Sugar Cane Technol. 2023, 31, 989–998. [Google Scholar]
  228. Kristini, A.; Samson, I.D.P.; BSES, M.D.N.S.; BSES, M. Integrated Pest Management of Stem Borers and Insect Vectors of Viral Diseases of Sugarcane in Indonesia. In Final Report; Australian Centre for International Agricultural Research: Sydney, Australia, 2023; 68p. [Google Scholar]
  229. January, B.; Rwegasira, G.M.; Tefera, F.T. Lepidopteran Stem Borer Species Abundance and Associated Damages on Irrigated Kilombero Lowland Rice Ecosystem in Tanzania. J. Entomol. 2018, 15, 28–35. [Google Scholar] [CrossRef]
  230. Lahr, J.; Buij, R.; Katagira, F.; Van Der Valk, H. Pesticides in the Southern Agricultural Growth Corridor of Tanzania (SAGCOT): A scoping study of current and future use, associated risks and identification of actions for risk mitigation. Wageningen Environ. Res. 2016, 2760, 71. [Google Scholar]
  231. Nwonuala, A.I. Deseases and Pests of Rice and Other Factors Limiting Rice Production in Rivers State; Department of Crop/Soil Science Rivers State University of Science and Technoogy: Port Harcourt, Nigeria, 2008; Available online: https://www.researchgate.net/profile/Ann-Ikwunma-Nwonuala/publication/296676698_Diseases_and_Pests_of_Rice_and_other_Factors_Limiting_Rice_production_in_Rivers_State/links/56d7f2aa08aebe4638af24dc/Diseases-and-Pests-of-Rice-and-other-Factors-Limiting-Rice-production-in-Rivers-State (accessed on 28 March 2025).
  232. Mulcahy, M.M. Improving the Deployment of Insecticidal Seed Treatments in Louisiana Rice in Accordance with Integrated Pest Management. Ph.D. Thesis, Louisiana State University and Agricultural & Mechanical College, Baton Rouge, LA, USA, 2021. [Google Scholar]
  233. Mohammed, I.G.; Bashiru, M.; Gbadeyan, S.T.; Ehirin, B.; Bakare, S.O.; Aliyu, U.; Shema, A.M. Available online: www.ncribjare.org (accessed on 27 February 2025).
  234. January, B.; Rwegasira, G.M.; Tefera, T. Farmers’ perceptions of rice production constraints and stem borers management practices in Tanzania. J. Agric. Sci. 2018, 10. [Google Scholar] [CrossRef]
  235. Dougoud, J.; Clottey, V.; Bateman, M.; Wood, A. Étude sur la Protection des Cultures Dans les Pays où le Programme ‘Centres d’Innovations Vertes pour le Secteur Agro-Alimentaire’ est Actif. Rapport National Pour le ProCIVA au Bénin; GIZ: Cotonou, Bénin, 2018. [Google Scholar]
  236. Seni, A.; Pal, R. Comparative efficacies of insecticides and botanicals against rice gall midge, Orseolia oryzae (Wood-Mason) and their effect on the parasitoid Platygaster oryzae in rice ecosystem of Odisha, India. Entomon 2021, 46, 263–268. [Google Scholar] [CrossRef]
  237. Faheem, M.; Sajjad, A.; Shafique, R.M.; Rehman, A.; Aslam, M.N. Field evaluation of different insecticides against wheat aphids and their natural enemies in Pakistan. Asian J. Agric. Biol. 2016, 4, 126–133. [Google Scholar]
  238. Shah, F.M.; Razaq, M.; Ali, A.; Han, P.; Chen, J. Comparative role of neem seed extract, moringa leaf extract and imidacloprid in the management of wheat aphids in relation to yield losses in Pakistan. PLoS ONE 2017, 12, e0184639. [Google Scholar] [CrossRef] [PubMed]
  239. Perkins, C.M. Relationship between Aphid Infestations, Aphid Management Regimes, and the Incidence of Barley Yellow Dwarf Virus in Soft Red Winter Wheat. Master’s Thesis, University of Tennessee, Knoxville, TN, USA, 2018. [Google Scholar]
  240. Shah, M.A.; Subhash, S.; Naga, K.C.; Sharma, S. Biology and management of aphids infesting potato. In Sustainable Management of Potato Pests and Diseases; Springer: Singapore, 2022; pp. 213–245. [Google Scholar]
  241. Tariq, R.M.S.; Mukhtar, T.; Ahmad, T.; Aziz, S.; Ahmad, Z.; Akhtar, S.; Ali, A. Hordeum vulgare: Diseases, Etiology, and Management. In Sustainable Winter Fodder; CRC Press: Boca Raton, FL, USA, 2021; pp. 165–198. [Google Scholar]
  242. Gill, S.; Kunkel, B. Nursery Management of Two Major Below-Ground Feeding Plant Pests: Root Mealybug, Rhizoecus sp. and Rice Root Aphid, Rhopalosiphum rufiabdominalis (Sasaki) (Hemiptera: Pseudococcidae and Aphididae). J. Environ. Hortic. 2021, 39, 131–137. [Google Scholar] [CrossRef]
  243. Naqqash, M.N. Insect-pests of potato: Importance and management. In Potato Production Worldwide; Academic Press: Cambridge, MA, USA, 2023; pp. 133–144. [Google Scholar]
  244. Kinjale, R.S.; Jalgaonkar, V.N.; Naik, K.V.; Hatwar, N.K.; Lad, S.S. Evaluation of the Efficacy of Some Insecticides Against Rice Yellow Stem Borer, Scirpophaga incertulas (Walker). J. Entomol. Zool. Stud. 2021, 9, 123–125. [Google Scholar] [CrossRef]
  245. Katel, S.; Lamshal, B.S.; Singh Yadav, S.P.; Timsina, S.; Mandal, H.R.; Kattel, S.; Adhikari, N. Efficacy of different insecticides against the yellow stem borer (Scirpophaga incertulus Walker) (Lepidoptera: Crambidae) in spring rice cultivation. Cogent Food Agric. 2023, 9, 2218254. [Google Scholar] [CrossRef]
  246. Islam, M.S.; Shimul Das, S.D.; Islam, K.S.; Arifa Rahman, A.R.; Huda, M.N.; Dash, P.K. Evaluation of different insecticides and botanical extracts against yellow stem borer, Scirpophaga incertulas in rice field. Int. J. Biosci. 2013, 3, 117–125. [Google Scholar]
  247. Khan, R.A.; Khan, J.A.; Jamil, F.F.; Hamed, M. Resistance of Different Basmati Rice Varieties to Stem Borers Under Different Control Tactics of IPM and Evaluation of Yield. Pak. J. Bot. 2005, 37, 319. [Google Scholar]
  248. Sylvain, N.M.; Manyangarirwa, W.; Tuarira, M.; Onesime, M.K. Effect of the Lepidoptera Stem Borers, Busseola fusca (Fuller) and Chilo partellus (Swinhoe) on Green Mealies Production. Int. J. Innov. Res. Dev. 2015, 4, 366–374. [Google Scholar]
  249. Rani, D.S.; Sri, C.N.S.; Kumar, K.A.; Venkatesh, M.N. Economic Evaluation and Efficacy of Various Insecticides Against Maize Stem Borers. J. Pharmacogn. Phytochem. 2018, 7, 15–20. [Google Scholar]
  250. Deole, S.; Dubey, V.K.; Dash, D. Determination of Persistence and Residual Toxicity of Different Insecticides Against Pink Stem Borer, Sesamia inferens on Maize Plant. Int. J. Chem. Stud. 2018, 6, 2761–2764. [Google Scholar]
  251. Sidar, Y.K.; Nirmal, A.; Gajbhiye, R.K.; Bisen, M.S.; Bhargav, P. Insect Pest Succession on Hybrid Maize and Management of Pink Stem Borer, Sesamia inferens Walker. J. Pharmacogn. Phytochem. 2017, 6, 143–150. [Google Scholar]
  252. Kumbhar, C.R.; Singh, S.P.N. Efficacy of Newer Insecticides Against Rice Borer Complex Under North Bihar Condition. J. Entomol. Zool. Stud. 2020, 8, 797–801. [Google Scholar]
  253. Fernandes, F.O.; Abreu, J.A.; Christ, L.M.; Rosa, A.P.S.A. Efficacy of insecticides against Spodoptera frugiperda (Smith, 1797). J. Agric. Sci. 2019, 11, 494–503. [Google Scholar] [CrossRef]
  254. Godoy, D.N.; Pretto, V.E.; de Almeida, P.G.; Weschenfelder, M.A.; Warpechowski, L.F.; Horikoshi, R.J.; Bernardi, O. Dose Effects of Flubendiamide and Thiodicarb against Spodoptera Species Developing on Bt and Non-Bt Soybean. Insects 2023, 14, 766. [Google Scholar] [CrossRef]
  255. Jameel, M.; Alam, M.F.; Fatma, H.; Singh, D.; Khan, M.A.; Qureshi, M.A.; Siddique, H.R. Flubendiamide induced genetic and cellular damages directly influence the life cycle of the oriental leaf worm, Spodoptera litura. Pestic. Biochem. Physiol. 2023, 193, 105448. [Google Scholar] [CrossRef]
  256. Guruprasad, G.S.; Race, M.O.; Guruprasad, G.S.; Udikeri, S.S. Baseline toxicity and ovicidal action of different insecticides on new invasive insect pest into India: Fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae). Preprints, 2024. [Google Scholar] [CrossRef]
  257. do Nascimento, A.R.B.; Rodrigues, J.G.; Kanno, R.H.; de Amaral, F.S.A.E.; Malaquias, J.B.; Silva-Brandão, K.L.; Omoto, C. Susceptibility monitoring and comparative gene expression of susceptible and resistant strains of Spodoptera frugiperda to lambda-cyhalothrin and chlorpyrifos. Pest Manag. Sci. 2023, 79, 2206–2219. [Google Scholar] [CrossRef] [PubMed]
  258. Zaidi, S.W.N.; Saddiq, B.; Afzal, M.B.S.; Banazeer, A.; Serrão, J.E.; Farooq, U.; Baloch, M.A.Z. First report of resistance in Spodoptera frugiperda (Lepidoptera: Noctuidae) to lambda-cyhalothrin from Pakistan: Baseline susceptibility, selection, occurrence of cross-resistance, realized heritability, and inheritance mode of resistance. J. Econ. Entomol. 2024, 117, 1636–1647. [Google Scholar] [CrossRef]
  259. Li, X.; Wang, Q.; Wang, X.; Wang, Z. Synergistic Effects of Graphene Oxide and Pesticides on Fall Armyworm, Spodoptera frugiperda. Nanomaterials 2022, 12, 3985. [Google Scholar] [CrossRef]
  260. Song, Z.; Li, C.; Tan, Y.; Shen, S.; Gong, Y.; Wang, Y.; Zhang, Z. Chlorantraniliprole emulsified with botanical oils effectively controls invasive pest Spodoptera frugiperda larvae in corn plant. J. Pest Sci. 2023, 96, 1429–1440. [Google Scholar] [CrossRef]
  261. Li, X.; Jiang, H.; Wu, J.; Zheng, F.; Xu, K.; Lin, Y.; Xu, H. Drip application of chlorantraniliprole effectively controls invasive Spodoptera frugiperda (Lepidoptera: Noctuidae) and its distribution in maize in China. Crop Prot. 2021, 143, 105474. [Google Scholar] [CrossRef]
  262. Francis, F.; Jacquemyn, H.; Delvigne, F.; Lievens, B. From diverse origins to specific targets: Role of microorganisms in indirect pest biological control. Insects 2020, 11, 533. [Google Scholar] [CrossRef]
  263. van Lenteren, J.C.; Bolckmans, K.; Köhl, J.; Ravensberg, W.J.; Urbaneja, A. Biological control using invertebrates and microorganisms: Plenty of new opportunities. BioControl 2018, 63, 39–59. [Google Scholar] [CrossRef]
  264. Alene, A.D.; Neuenschwander, P.; Manyong, V.M.; Coulibaly, O.; Hanna, R. The impact of IITA-led biological control of major pests in Sub-Saharan African agriculture. In IMPACT; IITA: Ibadan, Nigeria, 2005. [Google Scholar]
  265. Jackline, K.M. Major Pests of African Indigenous Vegetables in Tanzania and the Effects of Plant Nutrition on Spider Mite Management. Ph.D. Thesis, Universität Hannover, Hannover, Germany, 2021. [Google Scholar]
  266. Maina, U.M.; Galadima, I.B.; Gambo, F.M.; Zakaria, D.J. A review on the use of entomopathogenic fungi in the management of insect pests of field crops. J. Entomol. Zool. Stud. 2018, 6, 27–32. [Google Scholar]
  267. Kitheka, D.M. Identification and Validation of African Indigenous Knowledge Practices on Management of Crop Pests in Kitui West Sub-County. Ph.D. Thesis, South Eastern Kenya University, Kwa Vonza, Kenya, 2023. [Google Scholar]
  268. Nasiya Beegum, A.N. Characterization, Evaluation and Formulation of Beauveria bassiana (Bals.) Strains Against Rice Bug, Leptocorisa spp. (Hemiptera: Alydidae). Ph.D. Thesis, Department of Agricultural Entomology, College of Agriculture, Vellanikkara, Thrissur, India, 2021. [Google Scholar]
  269. Stanley, J.; Babu, K.S.; Prasad, G.S.; Kalaisekar, A.; Subbarayudu, B.; Gangaiah, B. Insect Pest Management in Millet Cropping Systems. In Integrated Pest Management in Diverse Cropping Systems; Apple Academic Press: Palm Bay, FL, USA, 2023; pp. 229–258. [Google Scholar]
  270. Agboton, B.V.; Hanna, R.; von Tiedemann, A. Molecular detection of establishment and geographical distribution of Brazilian isolates of Neozygites tanajoae, a fungus pathogenic to cassava green mite, in Benin (West Africa). Exp. Appl. Acarol. 2011, 53, 235–244. [Google Scholar] [CrossRef] [PubMed]
  271. Khan, Z.R.; James, D.G.; Midega, C.A.; Pickett, J.A. Chemical ecology and conservation biological control. Biol. Control 2008, 45, 210–224. [Google Scholar] [CrossRef]
  272. Khari, N.A.M.; Hamid, S.A. Efficacy of insecticides on black-headed stem borer, Chilo polychrysus Walker (Lepidoptera: Pyralidae) in glasshouse condition. Serangga 2021, 26, 255–270. [Google Scholar]
  273. Majidi-Shilsar, F. Pathogenicity of the Entomopathogenic Fungi Beauveria bassiana and Metarhizium anisopliae to the Striped Rice Stem Borer, Chilo suppressalis. J. Agric. Vet. Sci. 2017, 4, 552–555. [Google Scholar]
  274. Liang, A.; Zhang, Y.; Xu, X.; Wang, H.; Gong, C.; Hu, J.; Li, X.; Yang, J.; Peng, A.; Wang, X. Eco-friendly chitosan base chlorantraniliprole nano-pesticides for effective control of Chilo suppressalis (Walker) through bidirectional transport. Environ. Sci. Nano 2025, 12, 1214–1229. [Google Scholar] [CrossRef]
  275. Xia, X.; Liu, B.Q.; Yu, P.H.; Yu, Z.P.; Zhang, R.; Luo, G.H.; Fang, J.C. Antibiotic feeding changes the bacterial community of Chilo suppressalis and thereby affects its pesticide tolerance. BMC Microbiol. 2024, 24, 273. [Google Scholar] [CrossRef] [PubMed]
  276. Chen, G.; Li, Q.; Zhang, C.; Zhao, W.; Jurat-Fuentes, J.L.; Zhou, X.; Chen, F.; Yang, Y.; Han, L. Synergism of Cry1Ca toxicity by gut resident Enterococcus spp. in the rice stem borer, Chilo suppressalis. Int. J. Biol. Macromol. 2024, 257, 128654. [Google Scholar] [CrossRef]
  277. Yuan, X.H.; Song, L.W.; Zhang, J.J.; Zang, L.S.; Zhu, L.; Ruan, C.C.; Sun, G.Z. Performance of four Chinese Trichogramma species as biocontrol agents of the rice striped stem borer, Chilo suppressalis, under various temperature and humidity regimes. J. Pest Sci. 2012, 85, 497–504. [Google Scholar] [CrossRef]
  278. Niyaki, A.; Radjabi, R.; Allahyari, M.S. Social factors critical for adoption of biological control agents Trichogramma spp. egg parasitoid of rice stem borer Chilo suppressalis in North of Iran. Agric. Environ. Sci. 2010, 9, 133–139. [Google Scholar]
  279. Harris, K.M. Keynote address: Bioecology of Chilo species. Int. J. Trop. Insect Sci. 1990, 11, 467–477. [Google Scholar] [CrossRef]
  280. Murali-Baskaran, R.K.; Sridhar, J.; Sharma, K.; Jain, L.; Ghosh, P. Periodic colonization of Trichogramma japonicum for bio-control of yellow stem borer (Scirpophaga incertulas) in summer low-land rice (Oryza sativa). Indian J. Agric. Sci. 2024, 94, 484–488. [Google Scholar] [CrossRef]
  281. Ogah, E.O.; Nwilene, F.E. Review article incidence of insect pests on rice in Nigeria: A review. J. Entomol. 2017, 14, 58–72. [Google Scholar] [CrossRef]
  282. Bari, M.N.; Jahan, M.; Islam, K.S. Effects of temperature on the life table parameters of Trichogramma zahiri (Hymenoptera: Trichogrammatidae), an egg parasitoid of Dicladispa armigera (Chrysomelidae: Coleoptera). Environ. Entomol. 2015, 44, 368–378. [Google Scholar] [CrossRef]
  283. Bari, M.N.; Jahan, M.; Islam, K.S.; Ali, M.P. Host egg age and supplementary diet influence the parasitism activity of Trichogramma zahiri (Hymenoptera: Trichogrammatidae). J. Econ. Entomol. 2016, 109, 1102–1108. [Google Scholar] [CrossRef]
  284. Kalyanasundaram, M.; Kamala, I.M. Parasitoids. In Ecofriendly Pest Management for Food Security; Elsevier: Amsterdam, The Netherlands, 2016; pp. 109–138. [Google Scholar]
  285. Roy, P.; Uddin, M.M.; Islam, K.S.; Das, K.R. Efficacy of different botanical and chemical insecticides against rice hispa (Dicladispa armigera). Prog. Agric. 2017, 28, 64–72. [Google Scholar] [CrossRef]
  286. Soundararajan, R.P.; Chandrasekaran, M.; Chitra, N. Botanical Plant Products against Insect Pests of Rice. In Cutting Edge Research in Agricultural Sciences; Book Publisher International: Kolkata, India, 2020. [Google Scholar]
  287. Shakir, M.M.; Ahmed, S. Incidence of rice hispa, Dicladispa armigera (Chrysomelidae: Coleoptera) on sugarcane crop and its chemical control. J. Agric. Res. 2015, 53, 49–61. [Google Scholar]
  288. Rupesh Sharma, R.S.; Lakhi Ram, L.R.; Renu Devi, R.D. Efficacy of white muscardine fungus (Beauveria bassiana) on rice hispa (Dicladispa armigera). Indian J. Agric. Res. 2017, 51, 296–298. [Google Scholar]
  289. Huigens, M.E. On the Evolution of Wolbachia-Induced Parthenogenesis in Trichogramma Wasps. Ph.D. Thesis, Wageningen University and Research, Wageningen, The Netherlands, 2003. [Google Scholar]
  290. Chiasson, H.; Hill, S.B. Population density, development and behaviour of Diopsis longicornis and D. apicalis (Diptera: Diopsidae) on rice in the Republic of Guinee. Bull. Entomol. Res. 1993, 83, 5–13. [Google Scholar] [CrossRef]
  291. Bashyala, S.; Poudela, D.; Gautamb, B. A review on cultural practice as an effective pest management approach under integrated pest management. Trop. Agroecosyst. (TAEC) 2022, 3, 34–40. [Google Scholar]
  292. Virgile, K.K.; Didier, K.K.; Félicia, J.; Jacques-Edouard, Y.K.; Nozéné, B.B.; Noël, K.K.; Daouda, K. Antiappetizing and Repellent Effect of Biopesticides ASTOUN 50 EC and NECO 50 EC on Eldana saccharina Walker (Lepidoptera: Pyralidae) under in vitro Conditions. J. Appl. Life Sci. Int. 2023, 26, 11–25. [Google Scholar] [CrossRef]
  293. van Vuuren, B.J.; Potgieter, L.; Van Vuuren, J.H. An agent-based simulation model of Eldana saccharina Walker. Nat. Resour. Model. 2018, 31, e12153. [Google Scholar] [CrossRef]
  294. SASRI. Guidelines and Recommendations for Eldana Control in the South African Sugar Industry. 2005. Available online: https://sasri.org.za/wp-content/uploads/Sugarcane-Farming/Publications/eldana-manual.pdf (accessed on 14 January 2025).
  295. Conlong, D.E. Biological control of Eldana saccharina Walker in South African sugarcane: Constraints identified from 15 years of research. Int. J. Trop. Insect Sci. 1997, 17, 69–78. [Google Scholar] [CrossRef]
  296. Conlong, D.E.; Rutherford, R.S. Conventional and new biological and habitat interventions for integrated pest management systems: Review and case studies using Eldana saccharina Walker (Lepidoptera: Pyralidae). Integr. Pest Manag. Innov. Dev. Process 2009, 1, 241–261. [Google Scholar]
  297. Singh, K.M.; Kumawat, M.M. Arthropod biodiversity and conservation biological control in rice. Indian J. Entomol. 2020, 82, 374–384. [Google Scholar] [CrossRef]
  298. Souobou, M.; Nacro, S.; Ouattara, D. Natural enemies associated with rice stemborers in the Kou Valley, Burkina Faso. Int. J. Trop. Insect Sci. 2015, 35, 164–171. [Google Scholar]
  299. Perex, M.L.; Cadapan, E.P. The Efficacy of Trichogramma Species as Biological Control Agents Against Some Rice Insect Pests. 1986. Available online: https://thephilippineentomologist.org/2021/03/31/the-efficacy-of-trichogramma-species-as-biological-control-agents-against-some-rice-insect-pests/ (accessed on 14 January 2025).
  300. Singh, B.; Chatterjee, S. Relative efficacy of some biorational and microbial insecticides against yellow stem borer and whorl maggot of boro paddy. J. Biopestic. 2021, 14, 90–96. [Google Scholar] [CrossRef]
  301. Iqbal, S. Insect, Pest and Disease Management in Rice; Austin Publication: Irving, TX, USA, 2020; p. 85. [Google Scholar]
  302. Choo, H.Y.; Rice, W.C. Evaluation of microbial agents against rice pests. In Field Manual of Techniques in Invertebrate Pathology: Application and Evaluation of Pathogens for Control of Insects and Other Invertebrate Pests; Springer: Dordrecht, The Netherlands, 2007; pp. 393–409. [Google Scholar]
  303. Katti, G. Current Status, Potential of Biopesticides in Pest Management in Rice; Scientific Publishers: Jodhpur, India, 2014; p. 474. [Google Scholar]
  304. Kartikeyan, K.; Purushothaman, S.M.; Smitha, S.G.; Ajish, P.G. Efficacy of a new insecticide combination against major pests of paddy. Indian J. Plant Prot. 2012, 40, 276–279. [Google Scholar]
  305. El-Sheikh, M.F.; Hegazy, F.H.; Hendawy, A.S. Impact of biocide, insecticides, compost and mineral fertilizers treatments on the abundance of parasitoid and predator insects in rice fields. J. Plant Prot. Pathol. 2018, 9, 225–230. [Google Scholar] [CrossRef]
  306. Ogah, E.O.; Omoloye, A.A.; Nwilene, F.E.; Nwogbaga, A.C. Effect of neem seed kernel extracts in the management of rice stem borers in the field in Nigeria. Niger. J. Biotechnol. 2011, 23, 13–21. [Google Scholar]
  307. Ghahari, H.; Belokobylskij, S.A.; Gadallah, N.S.; Quicke, D.L.; Shaw, S.R. Subfamily Doryctinae Foerster, 1863. In Braconidae of the Middle East (Hymenoptera); Academic Press: Cambridge, MA, USA, 2022; pp. 294–312. [Google Scholar]
  308. Latévi, K.; Ouattara, D.; Nwilene, F.; Onaga, G.; Gnankiné, O.; Nacro, S. Evaluation of the Effectiveness of Four Biopesticides (Bacillus thuringiensis, Trichoderma sp., Neem Oil and Jatropha curcas Oil) and a Chemical Insecticide, Deltamethrin, Against Lepidoptera Rice Stem Borers in Western Burkina Faso. 2022. Available online: https://ssrn.com/abstract=4918959 (accessed on 14 January 2025).
  309. Bhat, A.A.; Tak, H.; Ahad, I.; War, W.A.; Rasool, J.; Sheikh, S.A.; Malik, I.M. Unveiling the Impact of Mythimna separata Walker (Lepidoptera: Noctuidae) on Agriculture: Insights into Host Range Biology and Biological Control: A Review. J. Exp. Agric. Int. 2024, 46, 248–261. [Google Scholar] [CrossRef]
  310. Sharma, H.C.; Sullivan, D.J.; Bhatnagar, V.S. Population dynamics and natural mortality factors of the Oriental armyworm, Mythimna separata (Lepidoptera: Noctuidae), in South-Central India. Crop Prot. 2002, 21, 721–732. [Google Scholar] [CrossRef]
  311. Dodiya, R.D.; Barad, A.H.; Pathan, N.P.; Raghunandan, B.L. Trichogramma: A Promising Biocontrol Agent. Int. J. Econ. Plants 2023, 10, 192–199. [Google Scholar]
  312. Navik, O.; Yele, Y.; Kedar, S.C.; Sushil, S.N. Biological control of fall armyworm Spodoptera frugiperda (J.E. Smith) using egg parasitoids, Trichogramma species (Hymenoptera: Trichogrammatidae): A review. Egypt. J. Biol. Pest Control 2023, 33, 118. [Google Scholar] [CrossRef]
  313. Hou, Y.Y.; Yang, X.; Zang, L.S.; Zhang, C.; Monticelli, L.S.; Desneux, N. Effect of oriental armyworm Mythimna separata egg age on the parasitism and host suitability for five Trichogramma species. J. Pest Sci. 2018, 91, 1181–1189. [Google Scholar] [CrossRef]
  314. Myint, Y.Y.; Bai, S.; Zhang, T.; Babendreier, D.; He, K.; Wang, Z. Ovipositional preference of Trichogramma dendrolimi and Trichogramma ostriniae strains from Myanmar on different host egg ages of Asian corn borer, Ostrinia furnacalis (Lepidoptera: Crambidae). Biocontrol Sci. Technol. 2022, 32, 700–714. [Google Scholar] [CrossRef]
  315. Montecalvo, M.; Navasero, M. Susceptibility of Pre-adult Biological Stages of Mythimna separata (Walker) (Lepidoptera: Noctuidae) to Three Entomopathogenic Fungi (Hypocreales). Philipp. Agric. Sci. 2023, 106, 7–14. [Google Scholar] [CrossRef]
  316. Kulkarni, N.S.; Lingappa, S. Pathogenicity of entomopathogenic fungus, Nomuraea rileyi (Farlow) Samson on lepidopterous pests. Karnataka J. Agric. Sci. 2002, 15, 293–298. [Google Scholar]
  317. Lin, D.J.; Zhou, J.X.; Ali, A.; Fu, H.Y.; Gao, S.J.; Jin, L.; Fang, Y. Biocontrol efficiency and characterization of insecticidal protein from sugarcane endophytic Serratia marcescens (SM) against oriental armyworm Mythimna separata (Walker). Int. J. Biol. Macromol. 2024, 262, 129978. [Google Scholar] [CrossRef]
  318. Patel, L.C. Efficacy of some insecticides against green leaf hopper, Nephotettix virescens Distant (Hemiptera: Cicadellidae) and brown plant hopper, Nilaparvata lugens Stål (Hemiptera: Delphacidae) in rice with safety to natural enemies. J. Entomol. Res. 2022, 46, 780–788. [Google Scholar] [CrossRef]
  319. Zhao, X.; Wu, C.; Wang, Y.; Cang, T.; Chen, L.; Yu, R.; Wang, Q. Assessment of toxicity risk of insecticides used in rice ecosystem on Trichogramma japonicum, an egg parasitoid of rice lepidopterans. J. Econ. Entomol. 2012, 105, 92–101. [Google Scholar] [CrossRef]
  320. Reddy, N.V. Impact of Bio-Intensive Pest Management Modules on Incidence of Pest and Their Natural Enemies in Rice. Ph.D. Thesis, Indira Gandhi Krishi Vishwavidyalaya, Raipur, India, 2021. [Google Scholar]
  321. Fowler, S.V.; Claridge, M.F.; Morgan, J.C.; Peries, I.D.R.; Nugaliyadde, L. Egg mortality of the brown planthopper, Nilaparvata lugens (Homoptera: Delphacidae) and green leafhoppers, Nephotettix spp. (Homoptera: Cicadellidae), on rice in Sri Lanka. Bull. Entomol. Res. 1991, 81, 161–167. [Google Scholar] [CrossRef]
  322. Abdullah, T.; Kuswinanti, T.; Nurariaty, A.; Daud, I.D.; Nasruddin, A.; Risal, R.; Tuwo, M. Application of Beauveria bassiana (Bals.) Vuil. (Hypocreales: Cordycipitaceae) in rice seed and its effect on mortality of green leaf hopper, Nephotettix virescens (Distant) (Homoptera: Cicadellidae). IOP Conf. Ser. Earth Environ. Sci. 2020, 486, 012150. [Google Scholar] [CrossRef]
  323. Ibrahim, E.; Firmansyah, F.; Panikkai, S. The effectiveness of the entomopathogenic fungus Metarhizium anisopliae in controlling the green leaf hopper (Nephotettix virescens). IOP Conf. Ser. Earth Environ. Sci. 2021, 9115, 012061. [Google Scholar] [CrossRef]
  324. Dave, P.P.; Singh, S.; Chodvadiya, M.B.; Choudhary, H. Bioefficacy of crude polyherbal formulations against hoppers (Insecta: Hemiptera) of rice. J. Entomol. Zool. Stud. 2020, 8, 1392–1398. [Google Scholar] [CrossRef]
  325. Paul, S.; Das, S. Natural insecticidal proteins, the promising bio-control compounds for future crop protection. Nucleus 2021, 64, 7–20. [Google Scholar] [CrossRef]
  326. Li, M.; Li, S.; Xu, A.; Lin, H.; Chen, D.; Wang, H. Selection of Beauveria isolates pathogenic to adults of Nilaparvata lugens. J. Insect Sci. 2014, 14, 32. [Google Scholar] [CrossRef]
  327. Sumikarsih, E.; Herlinda, S.; Pujiastuti, Y. Conidial density and viability of Beauveria bassiana isolates from Java and Sumatra and their virulence against Nilaparvata lugens at different temperatures. Agrivita J. Agric. Sci. 2019, 41, 335–350. [Google Scholar] [CrossRef]
  328. Zhang, X.; Li, K.; Wang, P.; Ma, M.; Tang, T.; Fu, W.; Tan, X. Harnessing Lecanicillium attenuatum: A novel strategy for combatting Nilaparvata lugens in rice fields. Pestic. Biochem. Physiol. 2024, 204, 106078. [Google Scholar] [CrossRef] [PubMed]
  329. Sujeetha, J.A.R.; Sahayaraj, K. Role of entomopathogenic fungus in pest management. In Basic and Applied Aspects of Biopesticides; Springer: New Delhi, India, 2014; pp. 31–46. [Google Scholar]
  330. Lou, Y.G.; Zhang, G.R.; Zhang, W.Q.; Hu, Y.; Zhang, J. Biological control of rice insect pests in China. Biol. Control 2013, 67, 8–20. [Google Scholar] [CrossRef]
  331. Adusei, S.; Azupio, S. Neem: A novel biocide for pest and disease control of plants. J. Chem. 2022, 2022, 6778554. [Google Scholar] [CrossRef]
  332. Gao, M.Q.; Hou, S.P.; Pu, D.Q.; Shi, M.; Ye, G.Y.; Chen, X.X. Multi-generation effects of Bt rice on Anagrus nilaparvatae, a parasitoid of the nontarget pest Nilaparvata lugens. Environ. Entomol. 2010, 39, 2039–2044. [Google Scholar] [CrossRef]
  333. IRRI Rice Knowledge Bank. Rice Caseworm. Available online: http://www.knowledgebank.irri.org/training/fact-sheets/pest-management/insects/item/rice-caseworm (accessed on 29 January 2025).
  334. Ali, M.P.; Nessa, B.; Khatun, M.T.; Salam, M.U.; Kabir, M.S. A way forward to combat insect pest in rice. Bangladesh Rice J. 2021, 25, 1–22. [Google Scholar] [CrossRef]
  335. Gogoi, H.; Bora, D. Bio-efficacy potential of some ethnically important plants against Nymphula depunctalis Guenée (Lepidoptera: Pyralidae) larvae with special reference to Calotropis procera and Zanthoxylum nitidum. Natl. Acad. Sci. Lett. 2012, 35, 169–175. [Google Scholar] [CrossRef]
  336. Frei, M.; Khan, M.A.M.; Razzak, M.A.; Hossain, M.M.; Dewan, S.; Becker, K. Effects of a mixed culture of common carp, Cyprinus carpio L., and Nile tilapia, Oreochromis niloticus (L.), on terrestrial arthropod population, benthic fauna, and weed biomass in rice fields in Bangladesh. Biol. Control 2007, 41, 207–213. [Google Scholar] [CrossRef]
  337. Halwart, M.; Litsinger, J.A.; Barrion, A.T.; Viray, M.C.; Kaule, G. Efficacy of common carp and Nile tilapia as biocontrol agents of rice insect pests in the Philippines. Int. J. Pest Manag. 2012, 58, 330–346. [Google Scholar] [CrossRef]
  338. Jaipal, S.; Malik, R.K.; Yadav, A.; Gupta, R. IPM issues in zero-tillage system in rice-wheat cropping sequence. Technol. Bull. 2005, 8, 32. [Google Scholar]
  339. Sureshan, P.M.; Kumar, P.G. Chalcidoid Parasitoids. In Parasitoids in Pest Management; CRC Press: Boca Raton, FL, USA, 2023; pp. 151–188. [Google Scholar]
  340. Allesh Sinu, P.; Nasser, M.; Dharmarajan, P. Host searching behavior and potential of an aquatic ichneumonid pupal parasitoid of rice caseworm (Parapoynx stagnalis) in an upland rice paddy agro-ecosystem of the Western Ghats, India. Biocontrol Sci. Technol. 2007, 17, 1037–1045. [Google Scholar] [CrossRef]
  341. Rahman, S.; Biswas, S.K.; Barman, N.C.; Ferdous, T. Plant extract as selective pesticide for integrated pest management. Biotechnol. Res. 2016, 2, 6–10. [Google Scholar]
  342. Ooi, A.C. Common insect pests of rice and their natural biological control. An illustrated guide to the insect pests that feed on rice plants and the organisms that feed on and control those pests. Utar Agric. Sci. J. 2015, 1, 49–59. [Google Scholar]
  343. Oyetunji, O.E.; Odebode, C.; Nwilene, F.; Togola, A.; Tamo, M. Effect of Beauveria bassiana and Metarhizium anisopliae on the adult African rice gall midge (AfRGM–Orseolia oryzivora). Arch. Phytopathol. Plant Prot. 2019, 52, 906–916. [Google Scholar] [CrossRef]
  344. Ayangbemi, B.T.; Pitan, O.R.; Nwilene, F.E.; Atayese, M.O. Influence of solvent medium on the bioefficacy of ten plant materials against adult African rice gall midge (AfRGM–Orseolia oryzivora). Afr. J. Agric. Sci. 2024, 4, 186–191. [Google Scholar]
  345. Adair, R.; Aybergenov, B.A.; Sultanov, R.A.; Abilbaeva, T.B.; Borowiec, N.; Thaon, M.; Bush, S. Galling Assemblages Associated with Australian Eucalyptus and Acacia. 2023. Available online: https://www.researchgate.net/profile/Waqar-Jaleel/publication/299746787_Assessment_of_economic_and_yield_loss_of_mango_due_to_infestation_of_mango_gall_and_blossom_midges_in_Pakistan/links/5704d66f08ae44d70ee06d9f/Assessment-of-economic-and-yield-loss-of-mango-due-to-infestation-of-mango-gall-and-blossom-midges-in-Pakistan.pdf (accessed on 20 October 2025).
  346. Mahieu, C.M.; te Biesebeek, J.D.; Graven, C. Inventarisatie van Gewasbescherming Toepasbaar in de Teelt van Cannabis Binnen Het. 2020. Available online: https://www.rivm.nl/publicaties/inventarisatie-van-gewasbescherming-toepasbaar-in-teelt-van-cannabis-binnen-experiment (accessed on 20 October 2025).
  347. Messelink, G.J.; van Holstein, R.; de Groot, E.B. Praktijkproef geïntegreerde gewasbescherming in freesia. Wagening. UR Glastuinb. 2008, 172, 364867. [Google Scholar]
  348. Cranshaw, W.; Wainwright-Evans, S. Cannabis sativa as a host of rice root aphid (Hemiptera: Aphididae) in North America. J. Integr. Pest Manag. 2020, 11, 15. [Google Scholar] [CrossRef]
  349. Dara, S.K. Strawberry IPM Study 2013: Managing Insect Pests with Chemical, Botanical, and Microbial Pesticides. Available online: https://ucanr.edu/blog/e-journal-entomology-and-biologicals/article/strawberry-ipm-study-2013-managing-insect-pests (accessed on 20 October 2025).
  350. Lee, J.Y.; Kang, S.W.; Kim, S.W. Relationship between agitation speed and the morphological characteristics of Verticillium lecanii CS-625 during spore production. Biotechnol. Bioprocess Eng. 2008, 13, 1–6. [Google Scholar] [CrossRef]
  351. Qazi, S.S.; Khachatourians, G.G. Insect pests of Pakistan and their management practices: Prospects for the use of entomopathogenic fungi. Biopest Int. 2005, 1, 13–24. [Google Scholar]
  352. Pests, B.G.I. Significance to the Horticulture Industry. J. Environ. Hortic. 2021, 39, 131–137. [Google Scholar]
  353. Tang, R.; Babendreier, D.; Zhang, F.; Kang, M.; Song, K.; Hou, M.L. Assessment of Trichogramma japonicum and T. chilonis as potential biological control agents of yellow stem borer in rice. Insects 2017, 8, 19. [Google Scholar] [CrossRef]
  354. Manjunath, T.M. The egg parasitoids, Trichogramma japonicum and Telenomus dignus seem to have doubtful impact on the regulation of rice yellow stem borer, Scirpophaga incertulas—It is time for a reality check. Insect Environ. 2023, 26, 463–467. [Google Scholar]
  355. Yadav, U.; Madhu, B. Efficacy of Biopesticides for the Management of Rice Yellow Stem Borer Scirpophaga incertulas (Walker) in Rice at Prayagraj, UP, India. Int. J. Plant Soil Sci. 2023, 35, 888–893. [Google Scholar]
  356. Chatterjee, S.; Mondal, P. Management of rice yellow stem borer, Scirpophaga incertulas Walker using some biorational insecticides. J. Biopestic. 2014, 7, 143. [Google Scholar] [CrossRef]
  357. Nagaraju, M.C. Management of yellow stem borer, Scirpophaga incertulas (Walker) and enumeration of soil arthropods in natural farming approaches of paddy ecosystem. Pharma Innov. 2023, 12, 4485–4491. [Google Scholar]
  358. Deshpande, P.P.; Kulkarni, U.S.; Undirwade, D.B.; Nagdeote, V.G. Evaluation of Trichogramma spp. against yellow stem borer (Scirpophaga incertulas Walker) on paddy. Pharma Innov. 2023, 12, 1904–1907. [Google Scholar]
  359. Yunus, M. Effectiveness of Trichogramma japonicum utilization for biological control agents on Scirpophaga incertulas in Indonesia. Asian J. Crop Sci. 2018, 10, 29–31. [Google Scholar] [CrossRef]
  360. Seni, A. Impact of certain essential oils and insecticides against major insect pests and natural enemies in rice. J. Cereal Res. 2019, 11, 252–256. [Google Scholar] [CrossRef]
  361. Astrodjojo, S.; Sudjud, S.; Das, S.S. Effectiveness test of parasitization by parasitoid Trichogramma japonicum in controlling white rice stem borer (Scirpophaga innotata). Int. J. Food Agric. Nat. Resour. 2021, 2, 25–30. [Google Scholar]
  362. Rahmawasiah, R.; Abadi, A.L.; Mudjiono, G.; Rizali, A. The effect of integrated pest management on Scirpophaga innotata population and natural enemies on rice field in South Sulawesi, Indonesia. Biodiversitas J. Biol. Divers. 2022, 23. [Google Scholar] [CrossRef]
  363. Nurkomar, I.; Putra, I.L.I.; Buchori, D.; Setiawan, F. Revisiting Classical Biological Control Through the New Associations Between the Invasive Pest Spodoptera frugiperda J.E. Smith (Lepidoptera: Noctuidae) and Local Parasitoids. 2023. Available online: https://www.preprints.org/manuscript/202310.1928/v1?utm_source=researchgate (accessed on 14 January 2025).
  364. Srikanth, J. Glimpses of Research on Biocontrol of Sugarcane Pests in India: Retrospect and Prospects. 2019. Available online: https://www.researchgate.net/publication/337495420_GLIMPSES_OF_RESEARCH_ON_BIOCONTROL_OF_SUGARCANE_PESTS_IN_INDIA_RETROSPECT_AND_PROSPECTS_REVIEW_ARTICLE (accessed on 14 January 2025).
  365. Rahimoon, M.Y.; Lanjar, A.G.; Bukero, A.; Hajano, J.-u.-d.; Rahimoon, S.-e.-A.; Nahiyoon, S.A. Evaluation of various botanical extracts against white stem borer, Scirpophaga innotata (Walker) in rice crops under field conditions. Pure Appl. Biol. 2023, 12, 1532–1540. [Google Scholar] [CrossRef]
  366. Pandey, S.; Aryal, S.; Aryal, L.N.; Timsina, K.P. Plant protection measures to promote organic farming in Nepal: Prospects and challenges. J. Agric. Nat. Resour. 2022, 5, 198–212. [Google Scholar] [CrossRef]
  367. Afifah, L.; Bayfurqon, F.M.; Siriyah, S.L. Control of Rice Stem Borer Scirpophaga sp. Using Trichogramma sp. J. Pengabdian kpd. Masyarakat 2019, 5, 99–107. [Google Scholar] [CrossRef]
  368. Ateyim, S.T.S.; Obeng-Ofori, D. Some aspects of the biology and behaviour of Sesamia nonagrioides botanephaga Tams and Bowden (Lepidoptera: Noctuidae), a major stem borer pest of maize in Southern Ghana. West Afr. J. Appl. Ecol. 2005, 8, 1. [Google Scholar] [CrossRef]
  369. Olembo, N.K.; M’mboyi, F.; Nyende, B.; Oyugi, K.; Ambani, L. Status of crop biotechnology in Sub-Saharan Africa: A cross-country analysis. In African Biotechnology Stakeholders Forum (ABSF); African Biotechnology Stakeholders Forum: Nairobi, Kenya, 2010. [Google Scholar]
  370. Tesfaye, K.; Seid, J.; Getnet, M.; Mamo, G. Agriculture under a changing climate in Ethiopia: Challenges and opportunities for research. Ethiop. J. Agric. Sci. 2016, 26, 67–86. [Google Scholar]
  371. Ojumoola, O.A. Bioecology of the Fall Armyworm, Spodoptera frugiperda J.E. Smith on Maize, Zea mays L. in the South-West, Nigeria. Ph.D. Thesis, University of Ibadan, Ibadan, Nigeria, 2021. [Google Scholar]
  372. Dhawan, A.K.; Kumar, V.; Grewal, G.K. Potential of neem (Azadirachta indica Juss) (Meliaceae: Rutales) in insect pest management. In Integrated Pest Management; Scientific Publishers: Jodhpur, India, 2013; p. 370. [Google Scholar]
  373. Wahedi, J.; David, D.; Danba, E.; Yisa, S.; Zakariya, R. Yield Performance of Maize Treated with Neem Seed Extracts against Stem Borers. Am. J. Exp. Agric. 2016, 12, 1–8. [Google Scholar] [CrossRef]
  374. Yang, G.Q.; Du, S.G.; Li, L.; Jiang, L.B.; Wu, J.C. Potential positive effects of pesticides application on Sesamia inferens (Walker) (Lepidoptera: Insecta). Int. J. Insect Sci. 2014, 6, IJIS-S16485. [Google Scholar] [CrossRef]
  375. Li, C.X.; Cheng, X.; Dai, S.M. Distribution and insecticide resistance of pink stem borer, Sesamia inferens (Lepidoptera: Noctuidae), in Taiwan. Formosan Entomol. 2011, 31, 39–50. [Google Scholar]
  376. Maurya, R.P.; Koranga, R.; Samal, I.; Chaudhary, D.; Paschapur, A.U.; Sreedhar, M.; Manimala, R.N. Biological control: A global perspective. Int. J. Trop. Insect Sci. 2022, 42, 3203–3220. [Google Scholar] [CrossRef]
  377. Pavani, T.; UmaMaheswari, T.; Sekhar, J.C. Evaluation of efficacy of different insecticides and bioagents against Sesamia inferens Walker in maize. Eur. J. Zool. Res. 2013, 2, 98–102. [Google Scholar]
  378. Kfir, R.; Overholt, W.A.; Khan, Z.R.; Polaszek, A. Biology and management of economically important lepidopteran cereal stem borers in Africa. Annu. Rev. Entomol. 2002, 47, 701–731. [Google Scholar] [CrossRef]
  379. Wale, M.; Schulthess, F.; Kairu, E.W.; Omwega, C.O. Distribution and relative importance of cereal stem borers and their natural enemies in the semi-arid and cool-wet ecozones of the Amhara State of Ethiopia. Ann. Soc. Entomol. Fr. 2006, 42, 389–402. [Google Scholar] [CrossRef]
  380. Abonyo, E.A. Establishment and Efficacy of Stem Borer Biological Control Agents Released in Kenya. Ph.D. Thesis, University of Nairobi, Nairobi, Kenya, 2019. [Google Scholar]
  381. Moyal, P.; Le Rue, B.; Van Den Berg, J.; Ratnadass, A.; Cugala, D.; Matama-Kauma, T.E.D.D.Y.; Defabachew, B. Morphological reinforcement, ancient introgressive hybridization and species delimitation in African stem-borer species of the genus Sesamia Guenée (Lepidoptera: Noctuidae). Syst. Entomol. 2011, 36, 421–434. [Google Scholar] [CrossRef]
  382. Sallam, M.N. Overseas Sugarcane Quarantine and Emergency Response Planning: SRDC Final Report BSS280. 2005. Available online: https://elibrary.sugarresearch.com.au/items/9440aa3f-be60-476e-8397-676e59de9c13 (accessed on 20 October 2025).
  383. Sallam, M.N.S. A review of sugarcane stem borers and their natural enemies in Asia and Indian Ocean Islands: An Australian perspective. Ann. Soc. Entomol. Fr. 2006, 42, 263–283. [Google Scholar] [CrossRef]
  384. Hailemichael, Y.; Schulthess, F.; Smith, J.W., Jr.; Overholt, W.A. Suitability of West African gramineous stemborers for the development of Cotesia species. Int. J. Trop. Insect Sci. 1997, 17, 89–95. [Google Scholar] [CrossRef]
  385. Hailemichael, Y.; Schulthess, F.; Smith, J.W., Jr.; Overholt, W.A. Physiological suitability of six West African gramineous borers (Lepidoptera: Noctuidae, Pyralidae) for development of Cotesia species complex (Hymenoptera: Braconidae). Int. J. Trop. Insect Sci. 2009, 29, 130–140. [Google Scholar] [CrossRef]
  386. Matama-Kauma, T.; Schulthess, F.; Le Rü, B.P.; Mueke, J.; Ogwang, J.A.; Omwega, C.O. Abundance and diversity of lepidopteran stemborers and their parasitoids on selected wild grasses in Uganda. Crop Prot. 2008, 27, 505–513. [Google Scholar] [CrossRef]
  387. Nikpay, A.; Vejar-Cota, G.; Budeguer, F.; Qin, Z.Q.; Perera, M.F.; Goebel, F.R. Advances in Seed Production and Management; Springer: Berlin/Heidelberg, Germany, 2021; p. 43. [Google Scholar]
  388. Tounou, A.K.; Gounou, S.; Borgemeister, C.; Goumedzoe, Y.M.D.; Schulthess, F. Susceptibility of Eldana saccharina (Lepidoptera: Pyralidae), Busseola fusca and Sesamia calamistis (Lepidoptera: Noctuidae) to Bacillus thuringiensis Cry toxins and potential side effects on the larval parasitoid Cotesia sesamiae (Hymenoptera: Braconidae). Biocontrol Sci. Technol. 2005, 15, 127–137. [Google Scholar] [CrossRef]
  389. Mahmood, S.; Parwez, H. The repository of biocontrol agents for Spodoptera frugiperda (Smith, 1797) with emphasis on their mode of action. J. Basic Appl. Zool. 2024, 85, 18. [Google Scholar] [CrossRef]
  390. Sahana, M.; Katti, P. Evaluation of biopesticides against fall armyworm, Spodoptera frugiperda in maize during kharif season. J. Eco-Friendly Agric. 2023, 18, 298–303. [Google Scholar] [CrossRef]
  391. Kenis, M.; Du Plessis, H.; Van den Berg, J.; Ba, M.N.; Goergen, G.; Kwadjo, K.E.; Polaszek, A. Telenomus remus, a candidate parasitoid for the biological control of Spodoptera frugiperda in Africa, is already present on the continent. Insects 2019, 10, 92. [Google Scholar] [CrossRef]
  392. Jin, T.; Lin, Y.; Ma, G.; Liu, J.; Hao, Z.; Han, S.; Peng, Z. Biocontrol potential of Trichogramma species against Spodoptera frugiperda and their field efficacy in maize. Crop Prot. 2021, 150, 105790. [Google Scholar] [CrossRef]
  393. Kenis, M. Prospects for classical biological control of Spodoptera frugiperda (Lepidoptera: Noctuidae) in invaded areas using parasitoids from the Americas. J. Econ. Entomol. 2023, 116, 331–341. [Google Scholar] [CrossRef]
  394. Fallet, P.; De Gianni, L.; Machado, R.A.; Bruno, P.; Bernal, J.S.; Karangwa, P.; Turlings, T.C. Comparative screening of Mexican, Rwandan and commercial entomopathogenic nematodes to be used against invasive fall armyworm, Spodoptera frugiperda. Insects 2022, 13, 205. [Google Scholar] [CrossRef]
  395. Mwamburi, L.A. Endophytic fungi, Beauveria bassiana and Metarhizium anisopliae, confer control of the fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae), in two tomato varieties. Egypt. J. Biol. Pest Control 2021, 31, 7. [Google Scholar] [CrossRef]
  396. Freire, Í.A.; Nascimento, I.N.D.; Rocha, G.T.; Santos, P.D.L.B.D.; Cunha, B.B.D.R.; Ferreira, A.D.C.D.L.; Monnerat, R.G. Production of Bacillus thuringiensis in “On Farm” Biofactories Is So Efficient Like a Commercial Product to Control Spodoptera frugiperda (Lepidoptera: Noctuidae). Agronomy 2024, 14, 2776. [Google Scholar] [CrossRef]
  397. Priyanka, M.; Yasodha, P.; Justin, C.G.L.; Ejilane, J.; Rajanbabu, V. Biorational management of maize fall armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) using Bacillus thuringiensis (Berliner) enriched with chemical additives. J. Appl. Nat. Sci. 2021, 13, 1231–1237. [Google Scholar]
  398. Amein, N.S. Toxicological and Biochemical Aspects of Bacillus thuringiensis var. kurstaki on Fall Armyworm, Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae). Egypt. Acad. J. Biol. Sci. F Toxicol. Pest Control 2023, 15, 63–68. [Google Scholar]
  399. AgriStudoc. Integrated Farming System: 9 Models, Objectives & Advantages. Available online: https://agristudoc.com/integrated-farming-system-models-objectives/ (accessed on 30 June 2025).
  400. Li, S.-X.; Jiang, J.; Lv, W.-G.; Siemann, E.; Woodcock, B.A.; Wang, Y.-Q.; Cavalieri, A.; Ba, N.-L.; Zhang, J.-Q.; Zheng, W.-Q.; et al. Rice-fish co-culture promotes multiple ecosystem services supporting increased yields. Agric. Ecosyst. Environ. 2025, 381, 109417. [Google Scholar] [CrossRef]
  401. Dossou-Yovo, E.R.; Arouna, A.; Bryan, E.; Claudia, R.; Futakuchi, K.; Grosjean, G.; Mujawamariya, G.; Rui, B.; Sarah, F.; Yossa, R. Stakeholders prioritization of climate-smart agriculture (CSA) in the rice-based production systems of Mali. AICCRA Report. 2021, p. 23. Available online: https://hdl.handle.net/10568/117537 (accessed on 20 October 2025).
  402. Freed, S.; Eam, D.; Tchetchan, B.; Dossou-Yovo, E.; Futakuchi, K.; Yossa, R. Rice-Fish Scoping Report for AICCRA Mali; Program Report: 2023-15; WorldFish: Penang, Malaysia, 2023. [Google Scholar]
  403. Akegbejo-Samsons, Y. Rice-fish production strategies in the coastal floodplains of Ondo State, Nigeria. In Second Africa Rice Congress: Innovation and Partnerships to Realize Africa’s Rice Potential; Semantic Scholar: Bamako, Mali, 2010; Available online: https://api.semanticscholar.org/CorpusID:55610328 (accessed on 20 October 2025).
  404. Rasowo, J.; Auma, E.; Ssanyu, G.; Ndunguru, M. Does African catfish (Clarias gariepinus) affect rice in integrated rice-fish culture in Lake Victoria Basin, Kenya? Afr. J. Environ. Sci. Technol. 2008, 2, 336–341. [Google Scholar]
  405. Bolay, F.K.; Trpis, M. Control of mosquitoes with Bacillus thuringiensis var. israelensis and larvivorous fish, Tilapia nilotica, in rice fields in Liberia, West Africa. Isr. J. Entomol. 1989, 23, 77–82. [Google Scholar]
  406. Simon, D.; Benhamou, J.F. Rice-fish farming in Guinée Forestière—Outcome of a rural development project. Field Actions Sci. Rep. 2009, 2, 49–56. [Google Scholar] [CrossRef]
  407. Baba, I.I.Y.; Abudulai, M.; Dogbe, W.; Heskaya, A. Integrated rice-fish farming as a business: The case of Golinga irrigation scheme small farmers. Int. J. Adv. Res. Agric. 2013, 1, 76–84. [Google Scholar]
  408. Long, P.; Huang, H.; Liao, X.; Fu, Z.; Zheng, H.; Chen, A.; Chen, C. Mechanism and capacities of reducing ecological cost through rice–Duck cultivation. J. Sci. Food Agric. 2013, 93, 2881–2891. [Google Scholar] [CrossRef] [PubMed]
  409. Linkui, C.; Xiaomei, Y. Method 7 Integrated rice-frog co-culture system. In Agroecological Rice Production in China; United Nations: Geneva, Switzerland, 2018; pp. 63–72. [Google Scholar] [CrossRef]
  410. Zou, Y.; Liu, Z.; Chen, Y.; Wang, Y.; Feng, S. Crop Rotation and Diversification in China: Enhancing Sustainable Agriculture and Resilience. Agriculture 2024, 14, 1465. [Google Scholar] [CrossRef]
  411. National Research Council; Committee on Pest; Pathogen Control Through Management of Biological Control Agents; Enhanced Cycles; Natural Processes. Ecologically Based Pest Management: New Solutions for a New Century; National Academies Press: Washington, DC, USA, 1996. [Google Scholar]
  412. Gomiero, T.; Pimentel, D.; Paoletti, M.G. Environmental impact of different agricultural management practices: Conventional vs. organic agriculture. Crit. Rev. Plant Sci. 2011, 30, 95–124. [Google Scholar] [CrossRef]
  413. Gamage, A.; Gangahagedara, R.; Gamage, J.; Jayasinghe, N.; Kodikara, N.; Suraweera, P.; Merah, O. Role of organic farming for achieving sustainability in agriculture. Farming Syst. 2023, 1, 100005. [Google Scholar] [CrossRef]
  414. Hajek, A.E.; Eilenberg, J. Natural Enemies: An Introduction to Biological Control; Cambridge University Press: Cambridge, UK, 2018. [Google Scholar]
  415. Straub, C.S.; Finke, D.L.; Snyder, W.E. Are the conservation of natural enemy biodiversity and biological control compatible goals? Biol. Control 2008, 45, 225–237. [Google Scholar] [CrossRef]
  416. Pretty, J.; Pervez Bharucha, Z. Integrated pest management for sustainable intensification of agriculture in Asia and Africa. Insects 2015, 6, 152–182. [Google Scholar] [CrossRef] [PubMed]
  417. Sarwar, S. Advancing Sustainable Agriculture: A Comprehensive Analysis of Integrated Pest Management Strategies in Global Rice Production. Int. J. Agric. Sustain. Dev. 2024, 6, 1–14. [Google Scholar]
  418. Sumner, D.R. Crop rotation and plant productivity. In Handbook of Agricultural Productivity; CRC Press: Boca Raton, FL, USA, 2018; pp. 273–314. [Google Scholar]
  419. Pargi Sanjay, J.; Gupta, P.; Balas, P.R.; Bambhaniya, V.U. Comparison between manual harvesting and mechanical harvesting. J. Sci. Res. Rep. 2024, 30, 917–934. [Google Scholar] [CrossRef]
  420. Nega, A. Climate change impacts on agriculture: A review of plant diseases and insect pests in Ethiopia and East Africa, with adaptation and mitigation strategies. Adv. Agric. 2025, 2025, 5606701. [Google Scholar] [CrossRef]
  421. Anaduaka, E.G.; Uchendu, N.O.; Asomadu, R.O.; Ezugwu, A.L.; Okeke, E.S.; Ezeorba, T.P.C. Widespread use of toxic agrochemicals and pesticides for agricultural products storage in Africa and developing countries: Possible panacea for ecotoxicology and health implications. Heliyon 2023, 9, e15173. [Google Scholar] [CrossRef]
  422. Gesesew, H.A.; Woldemichael, K.; Massa, D.; Mwanri, L. Farmers knowledge, attitudes, practices and health problems associated with pesticide use in rural irrigation villages, Southwest Ethiopia. PLoS ONE 2016, 11, e0162527. [Google Scholar] [CrossRef]
  423. Yarpuz-Bozdogan, N. The importance of personal protective equipment in pesticide applications in agriculture. Curr. Opin. Environ. Sci. Health 2018, 4, 1–4. [Google Scholar] [CrossRef]
  424. Mengistu, D.A.; Geremew, A.; Tessema, R.A. Pesticide safety practice and its public health risk in African regions: Systematic review and meta-analysis. BMC Public Health 2024, 24, 2295. [Google Scholar] [CrossRef]
  425. Ali, S.; Ullah, M.I.; Sajjad, A.; Shakeel, Q.; Hussain, A. Environmental and health effects of pesticide residues. In Sustainable Agriculture Reviews 48: Pesticide Occurrence, Analysis and Remediation Analysis? Springer Nature: London, UK, 2020; pp. 311–336. [Google Scholar]
  426. Haggblade, S.; Diarra, A.; Traoré, A. Regulating agricultural intensification: Lessons from West Africa’s rapidly growing pesticide markets. Dev. Policy Rev. 2022, 40, e12545. [Google Scholar] [CrossRef]
  427. He, Z.; Zhang, Z.; Valè, G.; San Segundo, B.; Chen, X.; Pasupuleti, J. Disease and pest resistance in rice. Front. Plant Sci. 2023, 14, 1333904. [Google Scholar] [CrossRef]
  428. Gurr, G.M.; Scarratt, S.L.; Wratten, S.D.; Berndt, L.; Irvin, N. Ecological engineering, habitat manipulation and pest management. In Ecological Engineering for Pest Management: Advances in Habitat Manipulation for Arthropods; CABI: Wallingford, UK, 2004; pp. 1–12. [Google Scholar]
  429. Zheng, Q.; Huang, W.; Xia, Q.; Dong, Y.; Ye, H.; Jiang, H.; Huang, S. Remote sensing monitoring of rice diseases and pests from different data sources: A review. Agronomy 2023, 13, 1851. [Google Scholar] [CrossRef]
  430. Alsadik, B.; Ellsäßer, F.J.; Awawdeh, M.; Al-Rawabdeh, A.; Almahasneh, L.; Elberink, S.O.; Al Asmar, Y. Remote sensing technologies using UAVs for pest and disease monitoring: A review centered on date palm trees. Remote Sens. 2024, 16, 4371. [Google Scholar] [CrossRef]
  431. Guebsi, R.; Mami, S.; Chokmani, K. Drones in Precision Agriculture: A Comprehensive Review of Applications, Technologies, and Challenges. Drones 2024, 8, 686. [Google Scholar] [CrossRef]
  432. McCarthy, C.; Nyoni, Y.; Kachamba, D.J.; Banda, L.B.; Moyo, B.; Chisambi, C.; Banfill, J.; Hoshino, B. Can Drones Help Smallholder Farmers Improve Agriculture Efficiencies and Reduce Food Insecurity in Sub-Saharan Africa? Local Perceptions from Malawi. Agriculture 2023, 13, 1075. [Google Scholar] [CrossRef]
  433. Raheem, D.; Dayoub, M.; Birech, R.; Nakiyemba, A. The contribution of cereal grains to food security and sustainability in Africa: Potential application of UAV in Ghana, Nigeria, Uganda, and Namibia. Urban Sci. 2021, 5, 8. [Google Scholar] [CrossRef]
  434. Heong, K.L.; Lu, Z.X.; Chien, H.V.; Escalada, M.; Settele, J.; Zhu, Z.R.; Cheng, J.A. Ecological engineering for rice insect pest management: The need to communicate widely, improve farmers’ ecological literacy and policy reforms to sustain adoption. Agronomy 2011, 11, 2208. [Google Scholar] [CrossRef]
  435. Evans, A. Ecological Engineering for Pest Management. J. Agric. Sci. 2005, 143, 326. [Google Scholar] [CrossRef]
  436. Zhu, P.; Zheng, X.; Johnson, A.C.; Chen, G.; Xu, H.; Zhang, F.; Gurr, G.M. Ecological engineering for rice pest suppression in China: A review. Agron. Sustain. Dev. 2022, 42, 69. [Google Scholar] [CrossRef]
  437. Brévault, T.; Renou, A.; Vayssieres, J.F.; Amadji, G.; Assogba-Komlan, F.; Diallo, M.D.; Clouvel, P. DIVECOSYS: Bringing together researchers to design ecologically-based pest management for small-scale farming systems in West Africa. Crop Prot. 2014, 66, 53–60. [Google Scholar] [CrossRef]
  438. Ratnadass, A. Crop protection for agricultural intensification systems in Sub-Saharan Africa. Sustain. Agric. Rev. 2020, 39, 1–34. [Google Scholar]
  439. Togola, A.; Beyene, Y.; Bocco, R.; Tepa-Yotto, G.; Gowda, M.; Too, A.; Boddupalli, P. Fall armyworm (Spodoptera frugiperda) in Africa: Insights into biology, ecology and impact on staple crops, food systems and management approaches. Front. Agron. 2025, 7, 1538198. [Google Scholar] [CrossRef]
  440. Ratto, F.; Bruce, T.; Chipabika, G.; Mwamakamba, S.; Mkandawire, R.; Khan, Z.; Sait, S.M. Biological control interventions reduce pest abundance and crop damage while maintaining natural enemies in Sub-Saharan Africa: A meta-analysis. Proc. R. Soc. B 2022, 289, 20221695. [Google Scholar] [CrossRef]
  441. Mengistie, B.T.; Mol, A.P.; Oosterveer, P. Pesticide use practices among smallholder vegetable farmers in Ethiopian Central Rift Valley. Environ. Dev. Sustain. 2017, 19, 301–324. [Google Scholar] [CrossRef]
  442. Dossou-Yovo, E.R.; Arouna, A.; Benfica, R.; Mujawamariya, G.; Yossa, R. A participatory framework for prioritizing climate-smart agriculture innovations in rice-based systems: A case study of Mali. Smart Agric. Technol. 2024, 7, 100392. [Google Scholar] [CrossRef]
  443. Wopereis, M.C.S.; Defoer, T. Moving methodologies to enhance agricultural productivity of rice-based lowland systems in Sub-Saharan Africa. In Advances in Integrated Soil Fertility Management in Sub-Saharan Africa: Challenges and Opportunities; Springer: Berlin/Heidelberg, Germany, 2007; pp. 1077–1091. [Google Scholar]
  444. Tambo, J.A.; Aliamo, C.; Davis, T.; Mugambi, I.; Romney, D.; Onyango, D.O.; Kansiime, M.; Alokit, C.; Byantwale, S.T. The impact of ICT-enabled extension campaign on farmers’ knowledge and management of fall armyworm in Uganda. PLoS ONE 2019, 14, e0220844. [Google Scholar] [CrossRef] [PubMed]
  445. Morepje, M.T.; Sithole, M.Z.; Msweli, N.S.; Agholor, A.I. The influence of E-commerce platforms on sustainable agriculture practices among smallholder farmers in Sub-Saharan Africa. Sustainability 2024, 16, 6496. [Google Scholar] [CrossRef]
  446. Adenle, A.A.; Azadi, H.; Manning, L. The era of sustainable agricultural development in Africa: Understanding the benefits and constraints. Food Rev. Int. 2018, 34, 411–433. [Google Scholar] [CrossRef]
Figure 1. Insect pests of rice plants in SSA [70,97,98,99,100,101,102,103].
Figure 1. Insect pests of rice plants in SSA [70,97,98,99,100,101,102,103].
Insects 16 01175 g001
Table 1. List of a few insect pests harmful to rice production in SSA.
Table 1. List of a few insect pests harmful to rice production in SSA.
Scientific NameCommon NamesOrder: FamilyDistributionReferences
A. armigeraShield Bug or grain stink bugHemiptera: PentatomidaeAcross SSA[23,28,29]
Chilo zacconius BleszynskiStriped stem borerLepidoptera: CrambidaeBenin, Cameroon, Côte d’Ivoire, Mali, Niger, Nigeria, Senegal, Sierra Leone[30,31,32]
Diopsis longicornis Macquart, Diopsis apicalis Dalman, Diopsis collaris WestwoodStalk-eyed fliesDiptera:
Diopsidae
Benin, BurkinaFaso, Cameroon, Chad, Côte d’Ivoire, Gambia, Ghana, Guinea, Guinea-Bissau, Liberia, Mali, Mauritania, Niger, Nigeria, Senegal, Sierra Leone, Togo[32,33]
Eldana saccharinaAfrican sugarcane stalk borerPyralidaeAcross SSA[34,35]
M. separatella RagonotAfrican white borerLepidoptera: PyralidaeCôte d’Ivoire, Mali, Nigeria[22,32]
O. oryzivoraAfrican rice gall midgeCecidomyiidaeAcross SSA[20,26,31]
Rhopalosiphum rufiabdominalisAfrican rice root aphidAphididaeAcross SSA[3,36]
Scirpophaga melanoclista MeyrickYellow stem borerLepidoptera: CrambidaeCameroon, Côte d’Ivoire, Mali, Nigeria, Senegal[32,37,38,39]
S. subumbrosa MeyrickYellow stem borerLepidoptera: CrambidaeGhana, Mali[32]
Sesamia calamistis HampsonPink stalk borerLepidoptera: NoctuidaeCameroon, The Gambia, Ghana, Côte d’Ivoire, Niger, Nigeria[22,32]
Sesamia nonagriodes botanephaga Tams & BowdenPink stalk borerLepidoptera: NoctuidaeGhana, Côte d’Ivoire, Nigeria[40,41]
Sesamia n. penniseti Tams and BowdenPink stalk borerLepidoptera: NoctuidaeGhana, Côte d’Ivoire, Nigeria[32,42]
Sesamia poephaga Tams and BowdenPink stalk borerLepidoptera: NoctuidaeNigeria[32]
Spodoptera frugiperdaFall armywormNoctuidaeAcross SSA[43,44,45]
Table 2. Summary of insect pests and transmitted diseases affecting rice production in SSA and their associated losses.
Table 2. Summary of insect pests and transmitted diseases affecting rice production in SSA and their associated losses.
Target InsectsDamageAffected StagesYield LossesReferences
Aphids
Aphis craccivora
A. gossypii
Myzus persicae
Sucking sap, causing yellowing and stunted growth From 20% to 80%[58,59]
Shield Bug or grain stink bug
A. armigera
Sucking sap from grains, causing grain weight loss and quality degradationCauses the most significant damage to rice during the milk stage, where it sucks sap from developing grains, leading to substantial yield and quality lossesUp to 70%[60,61]
Dark-headed stem borer
C. polychrysus
Boring into stems, causing deadhearts and whiteheads Up to 30%[62,63,64]
Striped stem borer
C. zacconius
C. suppressalis
Boring into stems, causing deadhearts and whiteheadsPrimarily affects rice during the tillering and booting stages.Up to 30%%[62,65]
Rice hispa
Dicladispa armigera
Leaf scraping, causing reduced photosynthesisPrimarily affects rice during the vegetative stage, which includes the seedling and tillering stages.From 10% to 62%[66,67,68]
Stalk-eyed flies
D. longicornis
D. apicalis
D. collaris
Feeding on rice plants, causing stunted growth and reduced yieldPrimarily affects rice during the tillering and flowering stages.From 10% to 15%[21,33,69,70]
African sugarcane stalk borer
E. saccharina
Boring into stems, causing deadhearts and whiteheadsDuring the late growth stages, particularly during the grain filling stage.Up to 50%[71,72]
Rice whorl maggot
Hydrellia philippina
Feeding on young leaves, causing stunted growth From 20% to 30%[73,74]
African white borer
M. separatella Ragonot
Boring into stems, causing deadhearts and whiteheads From 34.3% to 90.9%[75,76]
Rice armyworm
Mythimna separata
Defoliation, feeding on leaves and stems From 3% to 70%[77,78]
Rice leafhopper
Nephotettix virescens
Sucking sap, causing yellowing and stunted growth Up to 60%[79,80]
Brown planthopper
Nilaparvata lugens
Hopper burn, wilting, plant deathPrimarily affects rice during the tillering to booting stages.From 25% to 60%[81,82,83]
African rice gall midge
O. oryzivora
Gall formation, stunted growth, reduced tilleringPrimarily affects rice during the vegetative stage, which includes the seedling and tillering stages.Up to 100%[20,84,85]
Pink stalk borer
S. calamistis
S. nonagriodes botanephaga
S. n. penniseti
S. poephaga
S. inferens
The larvae tunnel into the stems, causing significant damage such as “dead hearts” (where the central shoot dies), broken stems, and reduced yield.Early growth stages, including the seedling and early tilleringFrom 25.7% to 78.9%[86,87,88]
Yellow stem borer
S. incertulas
Boring into stems, causing deadhearts and whiteheadsIt affects rice from the seedling stage through to maturity.From 3% to 87% [87,89,90]
Fall Armyworm
S. frugiperda
Defoliation, feeding on leaves and stems From 10% to 73%[91,92,93]
White Stem Borer
S. innotata
Boring into stems, causing deadhearts and whiteheadsPrimarily affects rice during the tillering and booting stages.Up to 80%[94,95,96]
Table 3. Rice Insect Pests in SSA and their Common Alternate Host Plants.
Table 3. Rice Insect Pests in SSA and their Common Alternate Host Plants.
Insect NamesWeed Hosts (Common and Scientific Names)References
C. zacconius BleszynskiBroadleaf Signalgrass (B. platyphylla), Crabgrass (Digitaria spp.)[126,127]
D. longicornis Macquart, D. apicalis Dalman, D. collaris WestwoodGoosegrass (E. indica), Johnsongrass (S. halepense)[128,129]
E. saccharinaBarnyardgrass (E. crus-galli), Yellow Nutsedge (Cyperus esculentus)[130,131,132]
M. separatella RagonotBroadleaf Signalgrass (B. platyphylla), Crabgrass (Digitaria spp.)[133,134]
O. oryzivoraBarnyardgrass (Echinochloa crus-galli), Yellow Nutsedge (Cyperus esculentus)[26,135]
R. rufiabdominalisGoosegrass (Eleusine indica), Johnsongrass (Sorghum halepense)[131,136]
S. melanoclista MeyrickGoosegrass (E. indica), Johnsongrass (Sorghum halepense)[56,137]
S. subumbrosa MeyrickBarnyardgrass (E. crus-galli), Yellow Nutsedge (Cyperus esculentus)[138,139]
S. calamistis HampsonBarnyardgrass (Echinochloa crus-galli), Johnsongrass (Sorghum halepense)[131,140]
S. nonagriodes botanephaga Tams & BowdenBarnyardgrass (E. crus-galli), Yellow Nutsedge (Cyperus esculentus)[82,141]
S. n. penniseti Tams and BowdenBroadleaf Signalgrass (Brachiaria platyphylla), Crabgrass (Digitaria spp.)[142,143,144]
S. poephaga Tams and BowdenGoosegrass (Eleusine indica), Johnsongrass (Sorghum halepense)[145,146,147]
S. frugiperdaBroadleaf Signalgrass (Brachiaria platyphylla), Crabgrass (Digitaria spp.)[148,149,150]
Table 4. List of a few genes/QTLs identified in rice to control insects along with resistance mechanism and donors.
Table 4. List of a few genes/QTLs identified in rice to control insects along with resistance mechanism and donors.
Target InsectsResistance SourcesGenes/QTLs/Resistance MechanismReferences
A. craccivoraIR64Rag1[160]
A. gossypiiIR36Cucurbitacin C[161]
C. polychrysus
(Dark-headed stem borer)
IR36Antibiosis: phenolic compounds affect the growth and development of larvae.[64]
IR50Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[162]
IR13429-57-1Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[163]
C. zacconius
C. suppressalis
(Striped stem borer)
Lac 23Antibiosis: phenolic compounds affect the growth and development of larvae.[164]
IR 2035-120-3Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[162]
IR 4625-132-1-2Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[165]
D. armigera
(Rice hispa)
Naggar DhanAntibiosis: phenolic compounds affect the growth and development of larvae.[166]
HPR 2617Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[166]
Sukara DhanAntibiosis: flavonoid and other biochemical compounds affect larval development and survival.[166,167]
D. longicornis
D. apicalis
D. collaris
(Stalk-eyed flies)
NERICA4Antibiosis: phenolic compounds affect the growth and development of larvae.[168]
NERICA1 and CG14Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[33,169]
NERICA16Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[170]
E. saccharina
(African sugarcane stalk borer)
WAB56-104Antibiosis: phenolic compounds affect growth and development.[171]
CG14Antixenosis: tannin and other biochemical compounds reduce the plant attractiveness.[172]
ITA306Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[172]
H. philippina
(Rice whorl maggot)
Swarna-Sub 1Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[173,174]
M. separata
(Rice armyworm)
IR36, IR64, TNAU Rice, and ADT 37Antibiosis: affects insect development and survival[175,176,177]
M. separatella Ragonot
(African white borer)
BG 90-2Antibiosis: phenolic compounds affect the growth and development of larvae.[30]
Basmati 217Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[178]
M27615Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[179]
M. persicaeIR72Mi-1.2[180]
N. virescens
(Rice leafhopper)
PTB33Grh2. Antibiosis: affects the growth and development of nymphs and adults, leading to high mortality.[181,182]
IR64Grh4. Antixenosis: reduces the attractiveness of the plant to the pest, leading to fewer eggs laid and lower survival rates.[181]
APL 796Antibiosis: phenolic compounds affect the growth and development of larvae.[183]
N. lugens
(Brown planthopper)
MudgoBph1[184]
ASD7Bph2[185]
Rathu HeenatiBph3[151]
BabaweeBph4[186]
ARC 10550Bph5[187]
SwarnalataBph6[185]
BalamaweeBph9[188]
IR65482-7-216-1-2Bph10[186,189]
B5 Bph14[190,191]
IR65482-7-216-1-2Bph18[186]
O. oryzivora
(African rice gall midge)
TOG7106Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[192,193]
TOS14519Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[33,193]
S. calamistis
S. nonagriodes botanephaga
S. n. penniseti
S poephaga,
S. inferens
(Pink stalk borer)
WAB56-104Antibiosis: phenolic compounds affect growth and development.[194]
CG14Antixenosis: tannin and other biochemical compounds reduce the plant attractiveness.[194]
ITA306Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[195,196,197,198]
S. frugiperda
(Fall Armyworm)
Miúdo BrancoAntixenosis: non-preference by insects [199]
IR 64Antibiosis: affects insect development and prolongs life cycle.[199]
Bacaba BrancoAntibiosis: affects insect development and reduces nutritional indices.[199]
S. incertulas
(Yellow stem borer)
TKM6Antibiosis: phenolic compounds affect the growth and development of larvae.[200,201]
IR36Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[202,203]
PTB33Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[204,205]
S. innotata
(White Stem Borer)
KSK-456Antibiosis: phenolic compounds affect the growth and development of larvae.[95]
PK 9586-8-2Antixenosis: secondary metabolites like catechetic tannins reduce the plant attractiveness.[206]
BRRI Dhan 64Antibiosis: flavonoid and other biochemical compounds affect larval development and survival.[207]
Table 5. List of Synthetic Pesticides used to Control Pests in SSA Rice Farms.
Table 5. List of Synthetic Pesticides used to Control Pests in SSA Rice Farms.
NamesCommercial NameActive IngredientsDose and ApplicationReferences
C. zacconius Bleszynski (Striped stem borer)Regent, Karate, Bulldock, VirtakoFipronil, Lambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole0.2 L/ha, 0.5 L/ha, 0.3 L/ha, 0.15 L/ha, foliar spray[21,216,217,218]
D. longicornis Macquart
D. apicalis Dalman
D. collaris Westwood
(Stalk-eyed flies)
Karate, Bulldock, Virtako, ConfidorLambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole, Imidacloprid0.5 L/ha, 0.3 L/ha, 0.15 L/ha, 0.25 L/ha, foliar spray[115,219,220,221,222]
E. saccharina (African sugarcane stalk borer)Bulldock, Karate, Virtako, ConfidorBeta-cyfluthrin, Lambda-cyhalothrin, Chlorantraniliprole, Imidacloprid0.3 L/ha, 0.5 L/ha, 0.15 L/ha, 0.25 L/ha, foliar spray[5,216,223,224,225,226,227,228]
M. separatella Ragonot (African white borer)Karate, Bulldock, Virtako, ConfidorLambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole, Imidacloprid0.5 L/ha, 0.3 L/ha, 0.15 L/ha, 0.25 L/ha, foliar spray[115,216,229,230,231,232]
O. oryzivora
(African rice gall midge)
Karate, Bulldock, Virtako, ConfidorLambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole, Imidacloprid0.5 L/ha, 0.3 L/ha, 0.15 L/ha, 0.25 L/ha, foliar spray[115,216,233,234,235,236]
R. rufiabdominalis (African rice root aphid)Confidor, Karate, Bulldock, VirtakoImidacloprid, Lambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole0.25 L/ha, 0.5 L/ha, 0.3 L/ha, 0.15 L/ha, foliar spray[216,237,238,239,240,241,242,243]
S. melanoclista Meyrick
(Yellow stem borer)
Fipronil
Cartap Hydrochloride
Fipronil
Cartap Hydrochloride
0.3 GR at 2.5 g/m2
4% GR at 1.9 g/m2
[244,245,246]
S. subumbrosa Meyrick
(Yellow stem borer)
ChlorpyriphosChlorpyriphos 75 WDG500–533 g/ha[207]
S. calamistis. Hampson
S. nonagriodes botanephaga Tams & Bowden
S. n. penniseti Tams and Bowden
S. poephaga Tams and Bowden
(Pink stalk borer)
Karate, Bulldock, Virtako, ConfidorLambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole, Imidacloprid0.5 L/ha, 0.3 L/ha, 0.15 L/ha, 0.25 L/ha, foliar spray[5,216,234,247,248,249,250,251,252]
S. frugiperda
(Fall armyworm)
Belt, Karate, Bulldock, VirtakoFlubendiamide, Lambda-cyhalothrin, Beta-cyfluthrin, Chlorantraniliprole0.2 L/ha, 0.5 L/ha, 0.3 L/ha, 0.15 L/ha, foliar spray[216,253,254,255,256,257,258,259,260,261]
Table 6. List of selected nature-based control options.
Table 6. List of selected nature-based control options.
Scientific NameCommon NamesNature-Based Control OptionsReferences
C. polychrysusDark-headed stem borerCotesia flavipes: A parasitoid wasp that targets the larvae.
Trichogramma chilonis: An egg parasitoid that targets the eggs.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Chlorantraniliprole nano-pesticides: Eco-friendly chitosan-based formulations for effective control.
[162,272,273]
C. suppressalisStriped stem borerTrichogramma japonicum: An egg parasitoid that targets the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Chlorantraniliprole nano-pesticides: Eco-friendly chitosan-based formulations for effective control.
[274,275,276,277,278]
C. zacconius BleszynskiStriped stem borerCotesia flavipes: A parasitoid wasp that targets the larvae.
Trichogramma chilonis: An egg parasitoid that targets the eggs
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
[38,115,279,280,281]
D. armigeraRice hispaTrichogramma zahiri: An egg parasitoid wasp that targets the eggs.
Neochrysocharis spp.: An egg and larval parasitoid effective.
Scutibracon hispae: A larval and pupal parasitoid.
Neem-based products: Neem oil and neem cake have been used.
Azacel: A commercial biopesticide that has shown high efficacy.
Larvocel: Another commercial biopesticide effective in reducing the population of Dicladispa armigera.
[282,283,284,285,286,287,288]
D. longicornis Macquart
D. apicalis Dalman
D. collaris Westwood
Stalk-eyed fliesTrichogramma chilonis: An egg parasitoid that targets the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Neem-based products: Neem oil and neem cake have been used.
[289,290,291]
E. saccharinaAfrican sugarcane stalk borerCotesia flavipes: A parasitoid wasp that targets the larvae.
Trichogramma chilonis: An egg parasitoid that targets the eggs.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
ASTOUN 50 EC: A biopesticide that has shown antiappetizing and repellent effects.
NECO 50 EC: Another biopesticide tested for its effects.
[292,293,294,295,296]
H. philippinaRice whorl maggotTrichogramma spp.: Egg parasitoids that target the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Neem-based products: Neem oil and neem cake have been used.
Flubendiamide: A biopesticide effective against the larvae.
Spinosad: Another biopesticide that has shown efficacy against the larvae.
[90,297,298,299,300,301,302,303,304,305]
M. separatella RagonotAfrican white borerChelonus maudae: A parasitoid wasp that targets the larvae.
Rhaconotus carinatus: Another parasitoid wasp effective against the larvae.
Pristomerus bullis: An ichneumonid wasp that parasitizes the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
[21,30,37,117,178,301,306,307,308]
M. separataRice armywormCotesia ruficrus: A parasitoid wasp that targets the larvae.
Trichogramma chilonis: An egg parasitoid effective.
Trichogramma dendrolimi: Another egg parasitoid used.
Nomuraea rileyi: An entomopathogenic fungus that infects and kills the larvae.
Bacillus thuringiensis (Bt): A bacterial biopesticide that produces toxins specifically targeting the larvae.
[309,310,311,312,313,314,315,316,317]
N. virescensRice leafhopperTrichogramma japonicum: An egg parasitoid that targets the eggs.
Anagrus spp.: Egg parasitoids that are effective against the egg.
Beauveria bassiana: An entomopathogenic fungus used for controlling the nymphs and adults.
Neem-based products: Neem oil and neem cake have been used.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the nymphs and adults.
[216,318,319,320,321,322,323,324,325]
N. lugensBrown planthopperBeauveria bassiana: An entomopathogenic fungus used for controlling the nymphs and adults.
Lecanicillium attenuatum: Another entomopathogenic fungus that has shown significant control efficacy.
Trichogramma japonicum: An egg parasitoid that targets the eggs.
Neem-based products: Neem oil and neem cake have been used.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the nymphs and adults.
[165,186,216,286,326,327,328,329,330,331,332]
N. depunctalisRice casewormSnails: Feed on the eggs.
Hydrophilid and Dytiscid water beetles: Feed on the larvae.
Spiders, Dragonflies, and Birds: Predate on the adult caseworms.
Parasitoids: Such as Elasmus spp., Apanteles spp., Bracon spp., and Pediobius spp.
Nuclear Polyhedrosis Virus: A potential pathogen for controlling N. depunctalis.
Plant Extracts: Extracts from Calotropis procera and Zanthoxylum nitidum have demonstrated significant insecticidal properties against N. depunctalis larvae.
[333,334,335,336,337,338,339,340,341]
O. oryzivoraAfrican rice gall midgePlatygaster diplosisae: A parasitoid wasp that targets the larvae.
Aprostocetus procereae: Another parasitoid wasp effective against the larvae.
Metarhizium anisopliae: An entomopathogenic fungus used for controlling the larvae.
Beauveria bassiana: Another entomopathogenic fungus effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Eucalyptus extracts: Effective in reducing the incidence of galls caused by the larvae.
[52,85,342,343,344,345]
R. rufiabdominalisAfrican rice root aphidStratiolaelaps scimitus (syn. Hypoaspis miles): A soil-dwelling predatory mite that targets the rice root aphid.
Beauveria bassiana: An entomopathogenic fungus that infects and kills the aphids.
Verticillium lecanii (now known as Lecanicillium lecanii): Another entomopathogenic fungus effective against aphids.
Beauveria bassiana (e.g., BotaniGard 22 WP, Mycotrol WPO): These biopesticides are applied to control root aphid populations by infecting and killing them.
[242,346,347,348,349,350,351,352]
S. incertulasYellow stem borerTrichogramma japonicum: An egg parasitoid that targets the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Telenomus rowani: Another egg parasitoid effective against the eggs.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Lemongrass oil: Effective in reducing the incidence of white ear heads.
[280,286,353,354,355,356,357,358,359,360]
S. innotataWhite Stem BorerTrichogramma japonicum: An egg parasitoid that targets the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Eucalyptus oil: Effective in reducing the incidence of white ear heads.
[361,362,363,364,365,366]
S. melanoclista Meyrick
S. subumbrosa Meyrick
Yellow stem borerTrichogramma japonicum: An egg parasitoid that targets the eggs.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Neem-based products: Neem oil and neem cake have been used.
Chlorantraniliprole nano-pesticides: Eco-friendly chitosan-based formulations for effective control.
[37,95,217,355,367]
S. calamistis HampsonPink stalk borerCotesia sesamiae: A parasitoid wasp that targets the larvae of Sesamia calamistis.
Metarhizium anisopliae: An entomopathogenic fungus effective against the larvae.
Beauveria bassiana: Another entomopathogenic fungus used for controlling the larvae.
Neem-based products: Neem oil and neem cake have been used.
[269,368,369,370,371,372]
Sesamia inferensPink stem borerCotesia flavipes: A parasitoid wasp that targets the larvae.
Tetrastichus howardi: A parasitoid wasp effective against the larvae.
Trichogramma spp.: Egg parasitoids that target the eggs.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
Beauveria bassiana: An entomopathogenic fungus used for controlling the larvae.
Neem-based products: Neem oil and neem cake have been used.
[261,373,374,375,376,377]
S. nonagriodes botanephaga Tams & BowdenPink stalk borerTrichogramma spp.: Egg parasitoids that target the.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
[214,370,378,379,380]
S. n. penniseti Tams and BowdenPink stalk borerCotesia sesamiae: Effective against the larvae.
Beauveria bassiana: Used to control the larvae.
Neem-based products: Effective in managing.
[381,382,383]
S. poephaga Tams and BowdenPink stalk borerCotesia sesamiae: Effective against the larvae.
Cotesia flavipes: A parasitoid wasp that targets the larvae.
Bacillus thuringiensis (Bt): A microbial insecticide effective against the larvae.
[384,385,386,387,388]
S. frugiperdaFall ArmywormTelenomus remus: A parasitoid wasp that targets the eggs.
Trichogramma pretiosum: Another egg effective parasitoid.
Chelonus insularis: A larval parasitoid that attacks the early stages of the pest.
Steinernema riobrave: An entomopathogenic nematode that infects and kills the larvae.
Metarhizium anisopliae: An entomopathogenic fungus effective against various stages of the pest.
Bacillus thuringiensis var. kurstaki (Bt): A bacterial biopesticide that produces toxins specifically targeting the larvae.
[389,390,391,392,393,394,395,396,397,398]
Table 7. Comparison between cultural, chemical, and biological control methods.
Table 7. Comparison between cultural, chemical, and biological control methods.
ComparisonCultural MethodChemical MethodBiological Method
Common Aim to control pests and diseases
Improve crop yield
Manual practicesUse of synthetic chemicalsUse of natural predators/pathogens
Crop rotationPesticides and herbicidesBiopesticides and beneficial insects
DifferencesWater managementQuick actionEnvironmentally friendly
Labor-intensivePotential resistance developmentSustainable
Lower costHigher costModerate cost
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Pegalepo, E.; Bocco, R.; Onaga, G.; Nwilene, F.; Tamò, M.; Togola, A.; Katiyar, S.K. Sustainable Insect Pest Management Options for Rice Production in Sub-Saharan Africa. Insects 2025, 16, 1175. https://doi.org/10.3390/insects16111175

AMA Style

Pegalepo E, Bocco R, Onaga G, Nwilene F, Tamò M, Togola A, Katiyar SK. Sustainable Insect Pest Management Options for Rice Production in Sub-Saharan Africa. Insects. 2025; 16(11):1175. https://doi.org/10.3390/insects16111175

Chicago/Turabian Style

Pegalepo, Esther, Roland Bocco, Geoffrey Onaga, Francis Nwilene, Manuele Tamò, Abou Togola, and Sanjay Kumar Katiyar. 2025. "Sustainable Insect Pest Management Options for Rice Production in Sub-Saharan Africa" Insects 16, no. 11: 1175. https://doi.org/10.3390/insects16111175

APA Style

Pegalepo, E., Bocco, R., Onaga, G., Nwilene, F., Tamò, M., Togola, A., & Katiyar, S. K. (2025). Sustainable Insect Pest Management Options for Rice Production in Sub-Saharan Africa. Insects, 16(11), 1175. https://doi.org/10.3390/insects16111175

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop