Sustainable Pest Management Strategies Under Greenhouse Conditions in Countries of the Global South
Abstract
1. Introduction
2. Materials and Methods
2.1. Eligibility Criteria
2.2. Search Strategy and Validation
2.3. Study Selection and Location Verification
2.4. Information Management
2.5. Selection and Classification of Information
3. Results and Discussion
3.1. Biological Target
3.2. Crops of Interest
3.3. Mentions by Control Strategies
3.3.1. Biological Control
3.3.2. Extracts and Chemical Compounds
3.3.3. Cultural Control
3.3.4. Other Strategies
4. Conclusions
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
| PRISMA | Preferred Reporting Items for Systematic reviews and Meta-Analyses |
| Qty | Quantity |
| PSO | Petroleum aerosol oil |
| NPV | Nucleopolyhedrovirus |
References
- Wyckhuys, K.A.G.; Fuentes, L.S.; Niño, N.E.; Espinosa, L.; De Vis, R.; Escobar, H. Manejo Integrado de Plagas y Enfermedades. In Manual de Producción de Tomate Bajo Invernadero; Editorial Utadeo: Bogotá, Colombia, 2010; pp. 85–117. [Google Scholar]
- Qu, C.; Yao, J.; Zhan, Q.; Zhang, D.; Li, Y.; Huang, J.; Wang, R. Risk Assessment, Cross-Resistance, Biochemical Mechanism and Fitness Cost of Tetraniliprole Resistance in the Tomato Pinworm Tuta absoluta. Crop Prot. 2024, 183, 106756. [Google Scholar] [CrossRef]
- Faria, M.; Souza, D.A.; Sanches, M.M.; Schmidt, F.G.V.; Oliveira, C.M.; Benito, N.P.; Lopes, R.B. Evaluation of Key Parameters for Developing a Metarhizium rileyi -based Biopesticide against Spodoptera frugiperda (Lepidoptera: Noctuidae) in Maize: Laboratory, Greenhouse, and Field Trials. Pest Manag. Sci. 2022, 78, 1146–1154. [Google Scholar] [CrossRef]
- Rashid, B.; Husnain, T.; Riazuddin, S. Herbicides and Pesticides as Potential Pollutants: A Global Problem. In Plant Adaptation and Phytoremediation; Springer: Berlin/Heidelberg, Germany, 2010; pp. 427–447. [Google Scholar] [CrossRef]
- Khan, B.A.; Nadeem, M.A.; Nawaz, H.; Amin, M.M.; Abbasi, G.H.; Nadeem, M.; Ali, M.; Ameen, M.; Javaid, M.M.; Maqbool, R.; et al. Pesticides: Impacts on Agriculture Productivity, Environment, and Management Strategies. In Emerging Contaminants and Plants; Springer: Berlin/Heidelberg, Germany, 2023; pp. 109–134. [Google Scholar] [CrossRef]
- Sindhu, S.S.; Sehrawat, A.; Sharma, R.; Khandelwal, A. Biological Control of Insect Pests for Sustainable Agriculture. Microorg. Sustain. 2017, 4, 189–218. [Google Scholar] [CrossRef]
- Moraes Boldini, J.; Prada Millán, Y.; Padilla Osorio, J.C.; Montenegro Gómez, S.P.; Fonseca Lara, M.R.; Mosquera Mena, R.A.; Pulido Pulido, S.Y. Control Biológico. In Servicios Ecosistémicos: Un Enfoque Introductorio con Experiencias del Occidente Colombiano; Universidad Nacional Abierta y a Distancia, UNAD: Bogotá, Colombia, 2019; pp. 201–211. [Google Scholar]
- Letourneau, D.K.; Armbrecht, I.; Rivera, B.S.; Lerma, J.M.; Carmona, E.J.; Daza, M.C.; Escobar, S.; Galindo, V.; Gutiérrez, C.; López, S.D.; et al. Does Plant Diversity Benefit Agroecosystems? A Synthetic Review. Ecol. Appl. 2011, 21, 9–21. [Google Scholar] [CrossRef] [PubMed]
- Wangari Nderitu, P.; Jonsson, M.; Arunga, E.; Otieno, M.; Jamleck Muturi, J.; Wafula, G.O. Combining Host Plant Resistance, Selective Insecticides, and Biological Control Agents for Integrated Management of Tuta absoluta. Adv. Agric. 2020, 2020, 1–8. [Google Scholar] [CrossRef]
- Dados, N.; Connell, R. The Global South. Contexts 2012, 11, 12–13. [Google Scholar] [CrossRef]
- Stanghellini, C.; Vaan’t Ooster, B.V.; Heuvelink, E. Greenhouse Horticulture: Technology for Optimal Crop Production, Second Edition; Wageningen Academic: Wageningen, The Netherlands, 2024; ISBN 978-90-04-69704-1. [Google Scholar]
- van Lenteren, J.C.; Alomar, O.; Ravensberg, W.J.; Urbaneja, A. Biological Control Agents for Control of Pests in Greenhouses. In Integrated Pest and Disease Management in Greenhouse Crops; Springer International Publishing: Cham, Switzerland, 2020; pp. 409–439. [Google Scholar]
- van Lenteren, J.C. A Greenhouse without Pesticides: Fact or Fantasy? Crop Prot. 2000, 19, 375–384. [Google Scholar] [CrossRef]
- Kumar, K.S.; Tiwari, K.N.; Jha, M.K. Design and Technology for Greenhouse Cooling in Tropical and Subtropical Regions: A Review. Energy Build. 2009, 41, 1269–1275. [Google Scholar] [CrossRef]
- Syed, A.R. Pest and Disease Management for Crop Production inside Greenhouses. Acta Hortic. 2006, 710, 89–102. [Google Scholar] [CrossRef]
- Weintraub, P.G. Integrated Control of Pests in Tropical and Subtropical Sweet Pepper Production. Pest Manag. Sci. 2007, 63, 753–760. [Google Scholar] [CrossRef]
- Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 Statement: An Updated Guideline for Reporting Systematic Reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
- Zuluaga-Hernández, C.D.; Hincapié, C.A.; Osorio, M. Non-Conventional Ingredients for Tilapia (Oreochromis Spp.) Feed: A Systematic Review. Fishes 2023, 8, 556. [Google Scholar] [CrossRef]
- Rethlefsen, M.L.; Kirtley, S.; Waffenschmidt, S.; Ayala, A.P.; Moher, D.; Page, M.J.; Koffel, J.B.; Blunt, H.; Brigham, T.; Chang, S.; et al. PRISMA-S: An Extension to the PRISMA Statement for Reporting Literature Searches in Systematic Reviews. Syst. Rev. 2021, 10, 39. [Google Scholar] [CrossRef] [PubMed]
- Chouikhi, S.; Assadi, B.H.; Lebdi, K.G.; Belkadhi, M.S. Efficacy of the Entomopathogenic Fungi Beauveria bassiana and Lecanicillium muscarium in the Control of the Tomato Leaf Miner, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae). Egypt. J. Biol. Pest Control 2022, 32, 1–8. [Google Scholar] [CrossRef]
- Somoza-Vargas, C.E.; Hernández-Velásquez, V.M.; Peña-chora, G.; Torres-García, G.; Huerta-de la Peña, A.; Ortega-Martínez, L.D.; Salazar-Magallón, J.A. Interaction of Beauveria bassiana Strain HPI-019/14 and Bacillus thuringiensis Strain GP139 for the Biological Control of Bemisia tabaci in Strawberry. Bull. Insectol. 2018, 71, 201–209. [Google Scholar]
- Gulzar, S.; Wakil, W.; Shapiro-Ilan, D.I. Combined Effect of Entomopathogens against Thrips tabaci Lindeman (Thysanoptera: Thripidae): Laboratory, Greenhouse and Field Trials. Insects 2021, 12, 456. [Google Scholar] [CrossRef]
- Wakil, W.; Ghazanfar, M.U.; Usman, M.; Hunter, D.; Shi, W. Fungal-Based Biopesticide Formulations to Control Nymphs and Adults of the Desert Locust, Schistocerca gregaria Forskål (Orthoptera: Acrididae): A Laboratory and Field Cage Study. Agronomy 2022, 12, 1160. [Google Scholar] [CrossRef]
- Jaber, L.R.; Araj, S.-E. Interactions among Endophytic Fungal Entomopathogens (Ascomycota: Hypocreales), the Green Peach Aphid Myzus persicae Sulzer (Homoptera: Aphididae), and the Aphid Endoparasitoid Aphidius colemani Viereck (Hymenoptera: Braconidae). Biol. Control 2018, 116, 53–61. [Google Scholar] [CrossRef]
- Al Khoury, C.; Guillot, J.; Nemer, N. Lethal Activity of Beauvericin, a Beauveria bassiana Mycotoxin, against the Two-spotted Spider Mites, Tetranychus urticae Koch. J. Appl. Entomol. 2019, 143, 974–983. [Google Scholar] [CrossRef]
- Michereff-Filho, M.; Navia, D.; Alexopoulos Quevedo, I.; de Almeida Magalhães, M.; Wagner da Silva Melo, J.; Biaggioni Lopes, R. The Effect of Spider Mite-Pathogenic Strains of Beauveria bassiana and Humidity on the Survival and Feeding Behavior of Neoseiulus Predatory Mite Species. Biol. Control 2022, 176, 105083. [Google Scholar] [CrossRef]
- Chouikhi, S.; Assadi, B.H.; Lebdi, K.G.; Belkadhi, M.S. Efficacy of the Entomopathogenic Fungus, Beauveria bassiana and Lecanicillium muscarium against Two Main Pests, Bemisia tabaci (Genn.) and Tetranychus urticae (Koch), under Geothermal Greenhouses of Southern Tunisia. Egypt. J. Biol. Pest Control 2022, 32, 125. [Google Scholar] [CrossRef]
- Núñez-Palenius, H.G.; Orosco-Alcalá, B.E.; Espitia-Vázquez, I.; Olalde-Portugal, V.; Hoflack-Culebro, M.; Ramírez-Santoyo, L.F.; Ruiz-Aguilar, G.M.L.; Cruz-Huerta, N.; Valiente-Banuet, J.I. Biological Control of Downy Mildew and Yield Enhancement of Cucumber Plants by Trichoderma harzianum and Bacillus subtilis (Ehrenberg) under Greenhouse Conditions. Horticulturae 2022, 8, 1133. [Google Scholar] [CrossRef]
- Izquierdo-García, L.F.; Cotes, A.M.; Moreno-Velandia, C.A. Screening for Effective Microbial Consortia against Fusarium Wilt of Cape Gooseberry (Physalis peruviana). BioControl 2021, 66, 713–725. [Google Scholar] [CrossRef]
- Affokpon, A.; Djihinto, A.C.; Coffi, E.N.D.; Coyne, D.L.; Coosemans, J. Root Endophytic Status of West African Biocontrol Agents and Implications for Root-Knot Nematode Management. Nematropica 2018, 48, 92–100. [Google Scholar]
- Raj, S.N.; Shetty, N.P.; Shetty, H.S. Synergistic Effects of Trichoshield on Enhancement of Growth and Resistance to Downy Mildew in Pearl Millet. BioControl 2005, 50, 493–509. [Google Scholar] [CrossRef]
- Sabir, N.; Deka, S.; Singh, B.; Sumitha, R.; Hasan, M.; Kumar, M.; Tanwar, R.; Bambawale, O. Integrated Pest Management for Greenhouse Cucumber: A Validation under North Indian Plains. Indian J. Hortic. 2011, 68, 357–363. [Google Scholar]
- Saravanan, T.; Muthusamy, M.; Marimuthu, T. Development of Integrated Approach to Manage the Fusarial Wilt of Banana. Crop Prot. 2003, 22, 1117–1123. [Google Scholar] [CrossRef]
- Limdolthamand, S.; Songkumarn, P.; Suwannarat, S.; Jantasorn, A.; Dethoup, T. Biocontrol Efficacy of Endophytic Trichoderma Spp. in Fresh and Dry Powder Formulations in Controlling Northern Corn Leaf Blight in Sweet Corn. Biol. Control 2023, 181, 105217. [Google Scholar] [CrossRef]
- Gómez-Valderrama, J.; Cuartas-Otálora, P.; Espinel-Correal, C.; Barrera-Cubillos, G.; Villamizar-Rivero, L. Fungal and Viral Entomopathogens as a Combined Strategy for the Biological Control of Fall Armyworm Larvae in Maize. CABI Agric. Biosci. 2022, 3, 24. [Google Scholar] [CrossRef]
- Naz, I.; Khan, R.A.A.; Masood, T.; Baig, A.; Siddique, I.; Haq, S. Biological Control of Root Knot Nematode, Meloidogyne incognita, in Vitro, Greenhouse and Field in Cucumber. Biol. Control 2021, 152, 104429. [Google Scholar] [CrossRef]
- Medina-Canales, M.G.; Terroba-Escalante, P.; Manzanilla-López, R.H.; Tovar-Soto, A. Assessment of Three Strategies for the Management of Meloidogyne arenaria on Carrot in Mexico Using Pochonia chlamydosporia Var. Mexicana under Greenhouse Conditions. Biocontrol Sci. Technol. 2019, 29, 671–685. [Google Scholar] [CrossRef]
- Mejía, C.; Espinel, C. In Vitro versus in Planta: Comparing the Compatibility of Akanthomyces lecanii with Pesticides against Trialeurodes vaporariorum. J. Appl. Entomol. 2022, 146, 1272–1280. [Google Scholar] [CrossRef]
- Abo-Elyousr, K.A.M.; Seleim, M.A.A.; Abd-El-Moneem, K.M.H.; Saead, F.A. Integrated Effect of Glomus mosseae and Selected Plant Oils on the Control of Bacterial Wilt Disease of Tomato. Crop Prot. 2014, 66, 67–71. [Google Scholar] [CrossRef]
- El-Ashry, R.M.; Ali, M.A.S.; Elsobki, A.E.A.; Aioub, A.A.A. Integrated Management of Meloidogyne incognita on Tomato Using Combinations of Abamectin, Purpureocillium lilacinum, Rhizobacteria, and Botanicals Compared with Nematicide. Egypt. J. Biol. Pest Control 2021, 31, 93. [Google Scholar] [CrossRef]
- Singh, H.; Kaur, T. Pathogenicity of Entomopathogenic Fungi against the Aphid and the Whitefly Species on Crops Grown under Greenhouse Conditions in India. Egypt. J. Biol. Pest Control 2020, 30, 84. [Google Scholar]
- Poitevin, C.G.; Porsani, M.V.; Poltronieri, A.S.; Zawadneak, M.A.C.; Pimentel, I.C. Fungi Isolated from Insects in Strawberry Crops Act as Potential Biological Control Agents of Duponchelia fovealis (Lepidoptera: Crambidae). Appl. Entomol. Zool. 2018, 53, 323–331. [Google Scholar] [CrossRef]
- Canassa, F.; D’Alessandro, C.P.; Sousa, S.B.; Demétrio, C.G.; Meyling, N.V.; Klingen, I.; Delalibera, I. Fungal Isolate and Crop Cultivar Influence the Beneficial Effects of Root Inoculation with Entomopathogenic Fungi in Strawberry. Pest Manag. Sci. 2020, 76, 1472–1482. [Google Scholar] [CrossRef]
- Taping, J.M.; Borja, B.T.; Bretaña, B.L.; Tanabe, M.E.; Cabasan, M.T. Fungal Endophytes as Potential Biocontrol Agent of Panama Disease of Banana. Egypt. J. Biol. Pest Control 2023, 33, 84. [Google Scholar] [CrossRef]
- Elkelany, U.S.; El-Mougy, N.S.; Abdel-Kader, M.M. Management of Root-Knot Nematode Meloidogyne incognita of Eggplant Using Some Growth-Promoting Rhizobacteria and Chitosan under Greenhouse Conditions. Egypt. J. Biol. Pest Control 2020, 30, 134. [Google Scholar] [CrossRef]
- Thuler, R.T.; Iost Filho, F.H.; De Oliveira Charlo, H.C.; De Bortoli, S.A. Effects of Rhizobacteria on the Biology and Behavior of Plutella xylostella (Lepidoptera: Plutellidae). Rev. Colomb. Entomol. 2017, 43, 195. [Google Scholar] [CrossRef]
- Esquivel-Cervantes, L.F.; Tlapal-Bolaños, B.; Tovar-Pedraza, J.M.; Pérez-Hernández, O.; Leyva-Mir, S.G.; Camacho-Tapia, M. Efficacy of Biorational Products for Managing Diseases of Tomato in Greenhouse Production. Plants 2022, 11, 1638. [Google Scholar] [CrossRef]
- Kamalakannan, A.; Shanmugam, V. Management Approaches of Maize Downy Mildew Using Biocontrol Agents and Plant Extracts. Acta Phytopathol. Entomol. Hung. 2009, 44, 255–266. [Google Scholar] [CrossRef]
- Mekonnen, H.; Kibret, M.; Assefa, F. Plant Growth Promoting Rhizobacteria for Biocontrol of Tomato Bacterial Wilt Caused by Ralstonia solanacearum. Int. J. Agron. 2022, 2022, 1–9. [Google Scholar] [CrossRef]
- Valan Arasu, M.; Al-Dhabi, N.A. Biological Control of Root Rot Disease-Causing Rhizoctonia solani in Tomato Plant by an Endophytic Fungus and Analysis of Growth Promoting Activities in Greenhouse and Field. Physiol. Mol. Plant Pathol. 2023, 127, 102080. [Google Scholar] [CrossRef]
- Vinchira-Villarraga, D.M.; Castellanos, L.; Moreno-Sarmiento, N.; Suarez-Moreno, Z.R.; Ramos, F.A. Antifungal Activity of Marine-Derived Paenibacillus Sp. PNM200 against Fusarium oxysporum f. Sp. Lycopersici, the Causal Agent of Tomato Vascular Wilt. Biol. Control 2021, 154, 104501. [Google Scholar] [CrossRef]
- Ndereyimana, A.; Nyalala, S.; Murerwa, P.; Gaidashova, S. Potential of Entomopathogenic Nematode Isolates from Rwanda to Control the Tomato Leaf Miner, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae). Egypt. J. Biol. Pest Control 2019, 29, 57. [Google Scholar] [CrossRef]
- Gulzar, S.; Wakil, W.; Shapiro-Ilan, D.I. Potential Use of Entomopathogenic Nematodes against the Soil Dwelling Stages of Onion Thrips, Thrips tabaci Lindeman: Laboratory, Greenhouse and Field Trials. Biol. Control 2021, 161, 104677. [Google Scholar] [CrossRef]
- Gulzar, S.; Usman, M.; Wakil, W.; Wu, S.; Oliveira-Hofman, C.; Srinivasan, R.; Toews, M.; Shapiro-Ilan, D. Virulence of Entomopathogenic Nematodes to Pupae of Frankliniella fusca (Thysanoptera: Thripidae). J. Econ. Entomol. 2021, 114, 2018–2023. [Google Scholar] [CrossRef] [PubMed]
- Usman, M.; Wakil, W.; Shapiro-Ilan, D.I. Entomopathogenic Nematodes as Biological Control Agent against Bactrocera zonata and Bactrocera dorsalis (Diptera: Tephritidae). Biol. Control 2021, 163, 104706. [Google Scholar] [CrossRef]
- Li, J.; Li, Y.; Wei, X.; Cui, Y.; Gu, X.; Li, X.; Yoshiga, T.; Abd-Elgawad, M.M.; Shapiro-Ilan, D.; Ruan, W.; et al. Direct Antagonistic Effect of Entomopathogenic Nematodes and Their Symbiotic Bacteria on Root-Knot Nematodes Migration toward Tomato Roots. Plant Soil 2023, 484, 441–455. [Google Scholar] [CrossRef]
- El Aalaoui, M.; Mokrini, F.; Dababat, A.A.; Lahlali, R.; Sbaghi, M. Moroccan Entomopathogenic Nematodes as Potential Biocontrol Agents against Dactylopius opuntiae (Hemiptera: Dactylopiidae). Sci. Rep. 2022, 12, 7590. [Google Scholar] [CrossRef] [PubMed]
- Walia, A.; Verma, S.C.; Sharma, P.L.; Sharma, N.; Palial, S. Relative Preference and Demographic Parameters of Encarsia formosa Gahan against Trialeurodes vaporariorum (Westwood). Egypt. J. Biol. Pest Control 2021, 31, 79. [Google Scholar] [CrossRef]
- Walia, A.; Verma, S.C.; Sharma, P.L.; Chandel, R.S.; Palial, S.; Sharma, N. Foraging Behaviour and Mutual Interference of Encarsia formosa Gahan Parasitizing Greenhouse Whitefly, Trialeurodes vaporariorum Westwood. Int. J. Trop. Insect Sci. 2022, 42, 807–813. [Google Scholar] [CrossRef]
- Castresana, J.; Rosenbaum, J.; Gagliano, E. The Transition from Chemical Pest Control to Biological Pest Management through the Transfer of Integrated Pest Management Techniques in Greenhouse Tomatoes in Concordia-Province of Entre Ríos, Argentina. Idesia 2019, 37, 17–27. [Google Scholar] [CrossRef]
- Gontijo, L.M.; Carvalho, R.M.R. Using Life Stage-Structured Matrix Models to Determine Natural Enemy: Pest Release Ratios for Augmentative Biological Control. J. Appl. Entomol. 2020, 144, 364–372. [Google Scholar] [CrossRef]
- Cherif, A.; Mansour, R.; Attia-Barhoumi, S.; Zappalà, L.; Grissa-Lebdi, K. Effectiveness of Different Release Rates of Trichogramma cacoeciae (Hymenoptera: Trichogrammatidae) against Tuta absoluta (Lepidoptera: Gelechiidae) in Protected and Open Field Tomato Crops in Tunisia. Biocontrol Sci. Technol. 2019, 29, 149–161. [Google Scholar] [CrossRef]
- Ahmadi, S.; Poorjavad, N. Behavioral and Biological Effects of Exposure to Tuta absoluta (Lepidoptera: Gelechiidae) Sex Pheromone on Several Trichogramma (Hymenoptera: Trichogrammatidae) Populations. J. Econ. Entomol. 2018, 111, 2667–2675. [Google Scholar] [CrossRef]
- Calvo, F.J.; Torres-Ruiz, A.; Velázquez-González, J.; Rodríguez-Leyva, E.; Lomeli-Flores, J.R. Improved Sweetpotato Whitefly and Potato Psyllid Control in Tomato by Combining the Mirid Dicyphus hesperus (Heteroptera: Miridae) With Specialist Parasitic Wasps. J. Econ. Entomol. 2018, 111, 549–555. [Google Scholar] [CrossRef]
- Mama Sambo, S.; Ndlela, S.; du Plessis, H.; Obala, F.; Mohamed, S.A. Identification, Microhabitat, and Ecological Niche Prediction of Two Promising Native Parasitoids of Tuta absoluta in Kenya. Insects 2022, 13, 496. [Google Scholar] [CrossRef]
- Elimem, M.; Harbi, A.; Limem-Sellemi, E.; Ben Othmen, S.; Chermiti, B. Orius laevigatus (Insecta; Heteroptera) Local Strain, a Promising Agent in Biological Control of Frankliniella occidentalis (Insecta; Thysanoptra) in Protected Pepper Crops in Tunisia. EuroMediterr. J. Environ. Integr. 2018, 3, 5. [Google Scholar] [CrossRef]
- Kordestani, M.; Mahdian, K.; Baniameri, V.; Sheikhi Garjan, A. Effect of Three Oviposition Feeding Substrates on Biology and Life Table Parameters of Orius laevigatus. Int. J. Trop. Insect Sci. 2021, 41, 1523–1529. [Google Scholar] [CrossRef]
- Calvo, F.J.; Torres-Ruiz, A.; Velázquez-González, J.C.; Rodríguez-Leyva, E.; Lomeli-Flores, J.R. Evaluation of Dicyphus hesperus for Biological Control of Sweet Potato Whitefly and Potato Psyllid on Greenhouse Tomato. BioControl 2016, 61, 415–424. [Google Scholar] [CrossRef]
- Wang, J.; Li, S.; Yang, J.; Guo, M.; Dai, H.; Ramirez-Romero, R.; Jin, Z.; Wang, S. The Fitness of Mass Rearing Food on the Establishment of Chrysopa pallens in a Banker Plant System under Fluctuating Temperature Conditions. Insects 2021, 12, 1014. [Google Scholar] [CrossRef]
- Morales, J.A.; Muñoz, L.Y.; Rodríguez Caicedo, D.; Cantor, F. Combined Action of Sex Pheromone and Wasp Apanteles gelechiidivoris in Greenhouse Tomato Crops. Acta Biolo. Colomb. 2014, 19, 175. [Google Scholar] [CrossRef]
- Lira, R.; Nascimento, D.V.; Torres, J.B.; Siqueira, H.A.A. Predation on Diamondback Moth Larvae and Aphid by Resistant and Susceptible Lady Beetle, Eriopis Connexa. Neotrop. Entomol. 2019, 48, 909–918. [Google Scholar] [CrossRef] [PubMed]
- Dalir, S.; Hajiqanbar, H.; Fathipour, Y.; Khanamani, M. A Comprehensive Picture of Foraging Strategies of Neoseiulus cucumeris and Amblyseius swirskii on Western Flower Thrips. Pest Manag. Sci. 2021, 77, 5418–5429. [Google Scholar] [CrossRef]
- Lahiri, S.; Yambisa, A. Efficacy of a Biopesticide and Predatory Mite to Manage Chilli Thrips, Scirtothrips dorsalis Hood (Thysanoptera: Thripidae) in Strawberry. Fla. Entomol. 2021, 104, 322–324. [Google Scholar] [CrossRef]
- Nicetic, O.; Watson, D.M.; Beattie, G.A.C.; Meats, A.; Zheng, J. Integrated Pest Management of Two-Spotted Mite Tetranychus urticae on Greenhouse Roses Using Petroleum Spray Oil and the Predatory Mite Phytoseiulus persimilis. Exp. Appl. Acarol. 2001, 25, 37–53. [Google Scholar] [CrossRef]
- Ayyub, M.B.; Nawaz, A.; Gogi, M.D.; Ahmad, J.N. Comparative Toxicity Assessment of Nuclear Polyhedrosis Virus and Spinosad against Spodoptera litura (FABRICIOUS) in Semi Field Conditions. Pak. J. Agric. Sci. 2020, 57, 445–450. [Google Scholar]
- Ayyub, M.B.; Nawaz, A.; Arif, M.J.; Amrao, L. Individual and Combined Impact of Nuclear Polyhedrosis Virus and Spinosad to Control the Tropical Armyworm, Spodoptera litura (Fabricius) (Lepidoptera: Noctuidae), in Cotton in Pakistan. Egypt. J. Biol. Pest Control 2019, 29, 67. [Google Scholar] [CrossRef]
- Alves, T.J.S.; Murcia-Meseguer, A.; Azpiazu, C.; Wanumen, A.; Wanderley-Teixeira, V.; Teixeira, Á.A.C.; Ortiz, A.; Medina, P. Side Effects of a Mixture of Essential Oils on Psyttalia concolor. Ecotoxicology 2020, 29, 1358–1367. [Google Scholar] [CrossRef] [PubMed]
- Passos, L.C.; Ricupero, M.; Gugliuzzo, A.; Soares, M.A.; Desneux, N.; Campolo, O.; Carvalho, G.A.; Biondi, A.; Zappalá, L. Sublethal Effects of Plant Essential Oils toward the Zoophytophagous Mirid Nesidiocoris tenuis. J. Pest Sci. 2022, 95, 1609–1619. [Google Scholar] [CrossRef]
- Mostafiz, M.M.; Hassan, E.; Shim, J.K.; Lee, K.Y. Insecticidal Efficacy of Three Benzoate Derivatives against Aphis gossypii and Its Predator Chrysoperla carnea. Ecotoxicol. Environ. Saf. 2019, 184, 109653. [Google Scholar] [CrossRef]
- da Silva Santana, A.; Luiz Lopes Baldin, E.; Paula Santana Lima, A.; Braga dos Santos, L.; Clezia dos Santos, M.; Manzini Vieira, T.; Miller Crotti Renata Takeara, E. New Challenges Demand New Solutions: Selected Essential Oils as an Alternative to Control Bemisia tabaci MED in Brazil. Crop Prot. 2022, 2, 105909. [Google Scholar] [CrossRef]
- Jaoko, V.; Taning, C.N.T.; Backx, S.; Motti, P.; Mulatya, J.; Vandenabeele, J.; Magomere, T.; Olubayo, F.; Mangelinckx, S.; Werbrouck, S.P.O.; et al. Laboratory and Greenhouse Evaluation of Melia volkensii Extracts for Potency against African Sweet Potato Weevil, Cylas puncticollis, and Fall Armyworm, Spodoptera frugiperda. Agronomy 2021, 11, 1994. [Google Scholar] [CrossRef]
- Marouf, A.E. Efficacy of Mandarin Crust Oil, Marigold Extract and Their Nanoemulsions, on Spodoptera littoralis (Boisd.) Larvae. Pak. J. Biol. Sci. 2022, 25, 688–697. [Google Scholar] [CrossRef]
- Hassan, E.; Mostafiz, M.M.; Iramu, E.T.; George, D.; Lee, K.Y. Evaluation of the Effect of Fungatol and Gamma-T-Ol on the Emergence and Adult Parasitoid Survival of Mummies of Cotton Aphids Parasitized by Aphidius Colemani. Insects 2022, 13, 38. [Google Scholar] [CrossRef]
- de Araújo, M.J.; da Câmara, C.A.; Born, F.D.; de Moraes, M.M. Acaricidal Activity of Binary Blends of Essential Oils and Selected Constituents against Tetranychus urticae in Laboratory/Greenhouse Experiments and the Impact on Neoseiulus californicus. Exp. Appl. Acarol. 2020, 80, 423–444. [Google Scholar] [CrossRef]
- Costa, E.M.; Silva, F.E.L.; Araujo, E.L. Effect of Aqueous Neem Seed Extract via Irrigation on Larvae of Liriomyza sativae in Melon Crop. Hortic. Bras. 2018, 36, 353–356. [Google Scholar] [CrossRef]
- Kishore, G.K.; Pande, S. Integrated Management of Late Leaf Spot and Rust Diseases of Groundnut (Arachis hypogaea L.) with Prosopis juliflora Leaf Extract and Chlorothalonil. Int. J. Pest Manag. 2005, 51, 325–332. [Google Scholar] [CrossRef][Green Version]
- Marques-Francovig, C.R.; Mikami, A.Y.; Dutra, V.; Carvalho, M.G.; Picareli, B.; Ventura, M.U. Organic Fertilization and Botanical Insecticides to Control Two-Spotted Spider Mite in Strawberry. Cienc. Rural 2014, 44, 1908–1914. [Google Scholar] [CrossRef]
- Ribeiro, R.C.; Zanuncio, T.V.; de Sousa Ramalho, F.; da Silva, C.A.; Serrão, J.E.; Zanuncio, J.C. Feeding and Oviposition of Anticarsia gemmatalis (Lepidoptera: Noctuidae) with Sublethal Concentrations of Ten Condiments Essential Oils. Ind. Crops Prod. 2015, 74, 139–143. [Google Scholar] [CrossRef]
- Adolfo Montes-Molina, J.; Gutiérrez-Miceli, F.; Manuel Ruíz-Valdiviezo, V. Characteristics of Tomato Plants Treated with Leaf Extracts of Neem (Azadirachta indica A. Juss. (L.)) and Mata-Raton (Gliricidia sepium (Jacquin)): A Greenhouse Experiment. J. Environ. Biol. 2014, 35, 935. [Google Scholar]
- Sabir, N.; Deka, S.; Tanwar, R. Comparative Evaluation of Pesticides and Biorationals against Key Pests of Greenhouse Chrysanthemum. Indian J. Hortic. 2012, 69, 101–105. [Google Scholar]
- Singh, R.; Koul, O.; Rup, P.J.; Jindal, J. Oviposition and Feeding Behavior of the Maize Borer, Chilo partellus, in Response to Eight Essential Oil Allelochemicals. Entomol. Exp. Appl. 2011, 138, 55–64. [Google Scholar] [CrossRef]
- Souza, C.M.; Baldin, E.L.L.; Ribeiro, L.P.; Silva, I.F.; Morando, R.; Bicalho, K.U.; Vendramim, J.D.; Fernandes, J.B. Lethal and Growth Inhibitory Activities of Neotropical Annonaceae-Derived Extracts, Commercial Formulation, and an Isolated Acetogenin against Helicoverpa armigera. J. Pest Sci. 2017, 90, 701–709. [Google Scholar] [CrossRef]
- Hussein, H.S.; Salem, M.Z.M.; Soliman, A.M. Repellent, Attractive, and Insecticidal Effects of Essential Oils from Schinus terebinthifolius Fruits and Corymbia citriodora Leaves on Two Whitefly Species, Bemisia tabaci, and Trialeurodes ricini. Sci. Hortic. 2017, 216, 111–119. [Google Scholar] [CrossRef]
- Salgado-Garciglia, R.; Molina-Torres, J.; López-Meza, J.E.; Damián, P.; Lara, L. Effect of Crude Extract and Bioactive Compounds of Heliopsis longipes on Anthracnose Incidence, Mycorrhization, and Nodulation of Bean. Agrociencia 2008, 42, 679–688. [Google Scholar]
- Cajias, E.; Vargas, H.; Estefane, F.; Bobadilla, D.D. Biological Activity of Lonchocarpus guaricensis Pittier in the Control of Larvae of Tuta absoluta (Meyrick). Rev. Fac. Cienc. Agrar. 2013, 45, 117–125. [Google Scholar]
- Castresan, J.E.; Rosenbaum, J.; González, L.A. Study of the Effectiveness of Three Essential Oils to Control Aphids on Pepper Plants, Capsicum annuum L. Idesia 2013, 31, 49–58. [Google Scholar] [CrossRef]
- Greenhill, M.; Cole, P.; Griffin, D. Evaluation of Pyrethrum for Use in Integrated Pest Management in Protected Cropping—A Review of Recent Research in Australia. Acta Hortic. 2015, 137–142. [Google Scholar] [CrossRef]
- Hajji-Hedfi, L.; Rebai, E.; Larayedh, A.; Regaieg, H.; Horrigue-Raouani, N. Biological control of Meloidogyne javanica on tomato with Dazitol® and soil solarization. Environ. Sci. Pollut. Res. 2018, 25, 17278–17282. [Google Scholar] [CrossRef]
- Rashidi, F.; Ganbalani, G.N. Toxicity and Sublethal Effects of Selected Insecticides on Life Parameters of Encarsia formosa (Hymenoptera: Aphelinidae), a Parasitoid of Trialeurodes vaporariorum (Hemiptera: Aleyrodidae). J. Entomol. Sci. 2018, 53, 543–553. [Google Scholar] [CrossRef]
- Bashiri, M.; Moharramipour, S.; Negahban, M. Developing a Vegetable Oil Formulation as a Safe Acaricide against Tetranychus urticae. J. Agric. Sci. Technol. 2021, 23, 1281–1295. [Google Scholar]
- Balanza, V.; Mendoza, J.E.; Cifuentes, D.; Bielza, P. Genetic Improvement of Spinosad Resistance in the Biocontrol Agent Orius laevigatus. BioControl 2021, 66, 673–685. [Google Scholar] [CrossRef]
- Abd El-Ghany, N.M.; Abdel-Razek, A.S.; Djelouah, K.; Moussa, A. Efficacy of Bio-Rational Insecticides against Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) on Tomatoes. Biosci. Res. 2018, 15, 28–40. [Google Scholar]
- Farahani, S.; Bandani, A.R.; Amiri, A. Toxicity and Repellency Effects of Three Essential Oils on Two Populations of Tetranychus urticae (Acari: Tetranychidae). Persian J. Acarol. 2020, 9, 67–81. [Google Scholar] [CrossRef]
- Awad, S.E.; Salah, K.B.H.; Jghef, M.M.; Alkhaibari, A.M.; Shami, A.A.; Alghamdi, R.A.; El-Ashry, R.M.; Ali, A.A.I.; El-Maghraby, L.M.M.; Awad, A.E. Chemical Characterization of Clove, Basil and Peppermint Essential Oils; Evaluating Their Toxicity on the Development Stages of Two-Spotted Spider Mites Grown on Cucumber Leaves. Life 2022, 12, 1751. [Google Scholar] [CrossRef]
- Born, F.D.; da Camara, C.A.; de Melo, J.P.; de Moraes, M.M. Acaricidal Property of the Essential Oil from Lippia Gracilis against Tetranychus urticae and a Natural Enemy, Neoseiulus californicus, under Greenhouse Conditions. Exp. Appl. Acarol. 2018, 75, 491–502. [Google Scholar] [CrossRef] [PubMed]
- Urbaneja-Bernat, P.; Holdcraft, R.; Hernández-Cumplido, J.; Rhodes, E.M.; Liburd, O.E.; Sial, A.A.; Mafra-Neto, A.; Rodriguez-Saona, C. Field, Semi-field and Greenhouse Testing of HOOK SWD, a SPLAT-based Attract-and-kill Formulation to Manage Spotted-wing Drosophila. J. Appl. Entomol. 2022, 146, 1230–1242. [Google Scholar] [CrossRef]
- Broughton, S.; Cousins, D.A.; Rahman, T. Evaluation of Semiochemicals for Their Potential Application in Mass Trapping of Frankliniella occidentalis (Pergande) in Roses. Crop Prot. 2015, 67, 130–135. [Google Scholar] [CrossRef]
- McCormick, A.L.C.; Karlsson, M.; Ochoa, C.F.B.; Proffit, M.; Bengtsson, M.; Zuluaga, M.V.; Fukumoto, T.; Oehlschlager, C.; Prado, A.M.C.; Witzgall, P. Mating Disruption of Guatemalan Potato Moth Tecia solanivora by Attractive and Non-Attractive Pheromone Blends. J. Chem. Ecol. 2012, 38, 63–70. [Google Scholar] [CrossRef] [PubMed]
- Chouikhi, S.; Assadi, B.H.; Ettaib, R.; Lebdi, K.G.; Belkadhi, M.S. Effectiveness of Mating Disruption Applied Alone or in Combination with Bioinsecticides against Tuta absoluta in Heated Greenhouse Tomato Crops of Southern Tunisia. Phytoparasitica 2023, 51, 521–532. [Google Scholar] [CrossRef]
- Jallow, M.F.A.; Dahab, A.A.; Albaho, M.S.; Devi, V.Y.; Jacob, J.; Al-Saeed, O. Efficacy of Mating Disruption Compared with Chemical Insecticides for Controlling Tuta absoluta (Lepidoptera: Gelechiidae) in Kuwait. Appl. Entomol. Zool. 2020, 55, 213–221. [Google Scholar] [CrossRef]
- Abou-Haidar, A.; Sobh, H.; Skinner, M.; Parker, B.; Abou-Jawdah, Y. Efficacy of Phytoseiulus persimilis and Amblyseius swirskii for Integrated Pest Management for Greenhouse Cucumbers under Mediterranean Environmental Conditions. Can. Entomol. 2021, 153, 598–615. [Google Scholar] [CrossRef]
- Lai, D.T.; Khuc, H.D.; Van Nguyen, L.; Hong, K.-J.; Nguyen, H.N. Potential of Using Mineral Oils for the Control of the Mosquito Bugs Helopeltis theivora (Hemiptera: Miridae) in Cashew Plantations. J. Asia. Pac. Entomol. 2022, 25, 101947. [Google Scholar] [CrossRef]
- Steiner, M.; Spohr, L.; Barchia, I.; Goodwin, S. Rapid Estimation of Numbers of Whiteflies (Hemiptera: Aleurodidae) and Thrips (Thysanoptera: Thripidae) on Sticky Traps. Aust. J. Entomol. 1999, 38, 367–372. [Google Scholar] [CrossRef]
- Pinto-Zevallos, D.M.; Vänninen, I. Yellow Sticky Traps for Decision-Making in Whitefly Management: What Has Been Achieved? Crop Prot. 2013, 47, 74–84. [Google Scholar] [CrossRef]
- Leoni, C.; Ghini, R. Sewage Sludge Effect on Management of Phytophthora nicotianae in Citrus. Crop Prot. 2006, 25, 10–22. [Google Scholar] [CrossRef][Green Version]
- Sharma, A.; Sharma, S.; Sabir, N.; El-Sheikh, M.A.; Alyemeni, M. Impact Assessment of Karanja Deoiled Cake and Sundried Biogas Slurry as a Mixed Substrate on the Nematicidal Potential of Purpureocillium lilacinum. J. King Saud Univ. Sci. 2021, 33, 101399. [Google Scholar] [CrossRef]
- Tomazeli, V.N.; Marchese, J.A.; Danner, M.A.; Perboni, A.T.; Finatto, T.; Crisosto, C.H. Improved Resistance to Disease and Mites in Strawberry, through the Use of Acibenzolar-S-Methyl and Harpin to Enhance Photosynthesis and Phenolic Metabolism. Theor. Exp. Plant Physiol. 2016, 28, 287–296. [Google Scholar] [CrossRef]
- De Lange, E.S.; Salamanca, J.; Polashock, J.; Rodriguez-Saona, C. Genotypic Variation and Phenotypic Plasticity in Gene Expression and Emissions of Herbivore-Induced Volatiles, and Their Potential Tritrophic Implications, in Cranberries. J. Chem. Ecol. 2019, 45, 298–312. [Google Scholar] [CrossRef]
- El-Ashry, R.M.; Nader, M.M.; Shami, A.; Alduwish, M.A.; Ahmed, A.E.; Alamoud, S.A.; Allohibi, A.; Alqahtani, F.S.; Alghamdi, A.M.; Ahmed, A.I.; et al. Ecofriendly Synthesis and Nematicidal Application of Copper Nanoparticles Fabricated from Bacillus subtilis AM18, against Root-Knot Nematode of Cucumber. Eur. J. Plant Pathol. 2024, 168, 53–81. [Google Scholar] [CrossRef]
- Shenashen, M.; Derbalah, A.; Hamza, A.; Mohamed, A.; El Safty, S. Antifungal Activity of Fabricated Mesoporous Alumina Nanoparticles against Root Rot Disease of Tomato Caused by Fusarium oxysporium. Pest Manag. Sci. 2017, 73, 1121–1126. [Google Scholar] [CrossRef]
- Nunez, E.; Barbosa, L.S.; Avelino-Capistrano, F. Efficiency of Capture of Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) with Mosquito Killer Light Traps. Agron. Colomb. 2023, 41, e106193. [Google Scholar] [CrossRef]
- Chouikhi, S.; Assadi, B.H.; Abbes, K.; Bkhiti, I.; Grissa Lebdi, K.; Belkadhi, M.S. Effectiveness of Mating Disruption with TUTATEC® Dispensers against Tuta absoluta (Lepidoptera: Gelechiidae) in Heated Greenhouses in Southern Tunisia. Phytoparasitica 2023, 51, 273–283. [Google Scholar] [CrossRef]
- Solis-Sánchez, L.O.; Castañeda-Miranda, R.; García-Escalante, J.J.; Torres-Pacheco, I.; Guevara-González, R.G.; Castañeda-Miranda, C.L.; Alaniz-Lumbreras, P.D. Scale Invariant Feature Approach for Insect Monitoring. Comput. Electron. Agric. 2011, 75, 92–99. [Google Scholar] [CrossRef]
- Solis-Sánchez, L.O.; García-Escalante, J.J.; Castañeda-Miranda, R.; Torres-Pacheco, I.; Guevara-González, R. Machine Vision Algorithm for Whiteflies (Bemisia tabaci Genn.) Scouting under Greenhouse Environment. J. Appl. Entomol. 2009, 133, 546–552. [Google Scholar] [CrossRef]
- Ghaderi, S.; Fathipour, Y.; Asgari, S. Population Density and Spatial Distribution Pattern of Tuta absoluta (Lepidoptera: Gelechiidae) on Different Tomato Cultivars. J. Agric. Sci. Technol. 2018, 20, 543–556. [Google Scholar]
- Scarlato, M.; Bao, L.; Rossing, W.A.H.; Dogliotti, S.; Bertoni, P.; Bianchi, F.J.J.A. Flowering Plants in Open Tomato Greenhouses Enhance Pest Suppression in Conventional Systems and Reveal Resource Saturation for Natural Enemies in Organic Systems. Agric. Ecosyst. Environ. 2023, 347, 108389. [Google Scholar] [CrossRef]
- Albornoz, M.V.; Flores, M.F.; Calderón, E.; Bahamondes, S.A.; Verdugo, J.A. Reproductive Behavior of Trialeurodes vaporariorum (Westwood) (Hemiptera: Aleyrodidae) Relative to Different Host Plants in an Intensive Tomato Crop Region of Chile. Horticulturae 2023, 9, 697. [Google Scholar] [CrossRef]
- Hata, F.T.; Ventura, M.U.; Carvalho, M.G.; Miguel, A.L.A.; Souza, M.S.J.; Paula, M.T.; Zawadneak, M.A.C. Intercropping Garlic Plants Reduces Tetranychus urticae in Strawberry Crop. Exp. Appl. Acarol. 2016, 69, 311–321. [Google Scholar] [CrossRef]
- Peres, F.S.C.; Fernandes, O.A.; Silveira, L.C.P.; Silva, C.S.B. da Marigold as Attractive Plant for Thrips in Protected Organic Melon Cultivation. Bragantia 2009, 68, 953–960. [Google Scholar] [CrossRef]
- El-Shafei, G.M.A.; Gotoh, T. Performance of Eighteen Tetranychid Mite Species (Acari: Tetranychidae) on Borage and Strawberry. Appl. Entomol. Zool. 2010, 45, 579–585. [Google Scholar] [CrossRef][Green Version]
- Steiner, M.Y.; Spohr, L.J.; Goodwin, S. Relative Humidity Controls Pupation Success and Dropping Behaviour of Western Flower Thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae). Aust. J. Entomol. 2011, 50, 179–186. [Google Scholar] [CrossRef]
- Gil, R.; Bojacá, C.R.; Rodríguez, M.Á. Adaptation of a Leaf Wetness Duration Model for Tomato under Colombian Greenhouse Conditions. Agron. Colomb. 2015, 33, 11–19. [Google Scholar] [CrossRef]
- Nur Hasyimah, R.; Nor Atikah, A.; Yaakop, S. The Significance of Free Air CO2 Enrichment and Open Roof Ventilation Greenhouse System in a Study of Mealworm Beetle, Tenebrio molitor L. (Coleoptera: Tenebrionidae). Serangga 2018, 122–129. [Google Scholar]
- Abreu, R.A.A.; Assis, F.A.; Souza, B.H.S.; Nascimento, A.M.; Latini, A.O.; Pio, L.A.S. Effects of Silicon Application on the Biochemistry of Passion Fruit and Performance of Dione juno juno (Lepidoptera: Nymphalidae). Arthropod-Plant Interact. 2021, 15, 417–429. [Google Scholar] [CrossRef]
- Rincon, D.F.; Rivera-Trujillo, H.F.; Mojica-Ramos, L.; Borrero-Echeverry, F. Sampling Plans Promoting Farmers’ Memory Provide Decision Support in Tuta absoluta Management. Agron. Sustain. Dev. 2021, 41, 33. [Google Scholar] [CrossRef]
- Messelink, G.J.; Lambion, J.; Janssen, A.; van Rijn, P.C.J. Biodiversity in and around Greenhouses: Benefits and Potential Risks for Pest Management. Insects 2021, 12, 933. [Google Scholar] [CrossRef]
- Altieri, M.A.; Nicholls, C.I. Soil Fertility Management and Insect Pests: Harmonizing Soil and Plant Health in Agroecosystems. Soil Tillage Res. 2003, 72, 203–211. [Google Scholar] [CrossRef]
- Ohyama, K.; Fujioka, J.; Sato, T.; Matsuo, T. System for Determining the Job Status of Individual Laborers in a Large-Scale Greenhouse. Comput. Electron. Agric. 2023, 206, 107661. [Google Scholar] [CrossRef]
- Ontiveros-Guerra, J.G.; Ramírez-Barrón, S.N.; Aguirre-Uribe, L.A.; Chacon-Hernandez, J.C.; Sánchez-Vega, M.; Cerna-Chávez, E.; García-López, J.I.; Neira-Vielma, A.A.; Meléndez-Ortíz, H.I.; Hernández-Juárez, A. Effect of Gold Nanoparticles Against Tetranychus urticae and Phytoseiulus persimilis in Tomato. Agronomy 2025, 15, 1684. [Google Scholar] [CrossRef]
- Rashid, T.S. Efficacy of Trichoderma Harzianum as a Natural Biocontrol and Growth-Promoting Agent Against Selected Tomato Fungal Pathogens. J. Phytopathol. 2025, 173, e70130. [Google Scholar] [CrossRef]
- Sosa, A.L.; Girardi, N.S.; Rosso, L.C.; Salusso, F.A.; Passone, M.A. Integrated Application of Biological and Biorational Strategies for Effective Control of the “False Root-Knot Nematode” in Tomato Plants. J. Pest Sci. 2025, 98, 1699–1714. [Google Scholar] [CrossRef]
- Bahoch, S.; Elaasri, A.; Chafiki, S.; Elame, F.; Wifaya, A.; Mayad, E.H.; Bouharroud, R.; Qessaoui, R. Biocontrol Potential of Rhizobacteria Against Passalora fulva and Tuta absoluta: A Sustainable Approach for Tomato Protection. Plants 2025, 14, 2672. [Google Scholar] [CrossRef] [PubMed]
- Magallanes-Tapia, M.A.; Cid del Prado-Vera, I.; Ferris, H.; Nava-Díaz, C.; González-Camacho, J.M.; Ochoa-Martínez, D.L. Pre-Plant Biofumigation and Integrated Post-Plant Strategies for Management of Nacobbus aberrans and Meloidogyne incognita in Greenhouse Tomato. Agronomy 2025, 15, 2284. [Google Scholar] [CrossRef]
- Xie, D.; Ismoilov, K.; Hu, S.; Wang, Q.; Chen, Z.; Zhou, W.; Ricupero, M.; Biondi, A.; Krutmuang, P.; Rodriguezsaona, C.; et al. Performance-Economy-Environment Multi-Criteria Assessment on an IPM Package Involving Fertilization Manipulation and Biological Pest Control: A Semi-Field Case Study on Tomato. Entomol. Gen. 2025, 45, 1159–1166. [Google Scholar] [CrossRef]
- Kaur, S.; Thakur, N.; Yadav, A.N. Exploring the Biopesticidal Potential of Indigenous Bacillus paramycoides EU-SIRCK1266 for Sustainable Management of Greenhouse Whiteflies Trialeurodes vaporariorum. J. Crop Health 2026, 78, 23. [Google Scholar] [CrossRef]
- Hyder, M.; Ali, F.; Ghafar, M.A.; Bukero, A.A.; Ul Haq, I.; Lodhi, A.M.; Hou, Y. Toxicity of Ethanolic Plant Extracts to Aphis gossypii, Bemisia tabaci, and Frankliniella occidentalis and Selectivity to Coccinella septempunctata and Menochilus sexmaculatus. Neotrop. Entomol. 2025, 54, 87. [Google Scholar] [CrossRef]
- Adss, I.A.A.; R Bayoumi, S.; Heikal, H.M.; Sobhy, S.E.; Saleh, A.A.; Hafez, E.E. Impact of Trichoderma, Abscisic Acid and Polyamines on Resistance Tomato Cultivars against M. incognita Infection. Mol. Biol. Rep. 2025, 52, 625. [Google Scholar] [CrossRef]
- Golizadeh, A.; Afshari, F. Effects of Organic and Inorganic Fertilizers on Life History Parameters of the Tomato Leafminer, Tuta absoluta on Two Tomato Cultivars. Crop Prot. 2025, 196, 107271. [Google Scholar] [CrossRef]
- Razmjou, J.; Mardani-Talaee, M.; Perumal, V. Investigating the Alleviatory Ability of Bio-Synthesized Zinc Oxide Nanoparticles from Sargassum ilicifolium (Turner) C. Agardh on the Tomato Plants Exposed to Whitefly Infestation. Sci. Rep. 2025, 15, 44206. [Google Scholar] [CrossRef]
- Zayed, M.S.; Hegab, M.A.M.S.; SaadAllah, M.S.; Elnabawy, E.S.M.; El-Beltagi, H.S.; Abo-Ogiala, A.M.; El-Harariy, A. Non- Conventional Agents Enhance Sweet Pepper (Capsicum annuum L. Var. Annuum) Defense against Aphis gossypii, Thrips tabaci, and Their Predators Chrysoperla carnea and Orius insidiosus. Glob. Chall. 2026, 10, e00590. [Google Scholar] [CrossRef] [PubMed]
- Rezaei, A.; Khanjani, M.; Farrokhi, S. Induced Resistance in Bell Pepper by Trichoderma harzianum and Jasmonic Acid against Frankliniella occidentalis (Thysanoptera: Thripidae). J. Entomol. Soc. Iran 2025, 45, 393–407. [Google Scholar] [CrossRef]
- Caplik, D.; Küsek, M. Biocontrol Potential of Acinetobacter Lactucae and Pseudarthrobacter Polychromogenes in Managing Pepper Bacterial Spot Disease. J. Phytopathol. 2025, 173, e70140. [Google Scholar] [CrossRef]
- Mardani-Talaee, M.; Nouri-Ganblani, G.; Razmjou, J.; Hassanpour, M.; Perumal, V.; Naseri, B. Bottom-Up Effects of Various Plant Growth Promoting Treatments on Fitness Parameters of Hippodamia variegata. J. Basic Microbiol. 2025, 65, e2400486. [Google Scholar] [CrossRef] [PubMed]
- Aghazadeh, A.; Negahban, M.; Fathipour, Y. Sublethal Impacts of a Commercial Botanical Pesticide (Salpipest®) Containing Nanoencapsulated Essential Oil of Wild Pistachio on Demographic Parameters of the Predatory Mite Amblyseius swirskii Feed on Greenhouse Whitefly. Neotrop. Entomol. 2025, 54, 27. [Google Scholar] [CrossRef] [PubMed]
- Mardani-Talaee, M.; Razmjou, J.; Nouri-Ganbalani, G.; Hassanpour, M.; Naseri, B. Bottom-up Effects of Different Fertilizer on Changes in the Two Sex Life Table of the Ladybug Beetle Adalia bipunctata L. Plant Prot. 2025, 48, 33–53. [Google Scholar] [CrossRef]
- Aziz, B.A.; Marzani, Q.A. Integrated Management of Strawberry Crown and Root Rot Caused by Fusarium Solani in Greenhouse Conditions. Polytech. J. 2025, 15, 64–74. [Google Scholar] [CrossRef]
- Kallali, N.S.; El Alami, N.; Laasli, S.E.; Broulaye, S.; Benseddik, Y.; Khfif, K.; Boutaleb-Joutei, A.; Ouijja, A.; Mokrini, F.; Lahlali, R. Potential of Moroccan Entomopathogenic Nematodes in Controlling Polyphagous Fruit Flies, Drosophila melanogaster (Meigen, 1830) and D. Simulans (Sturtevant, 1919), under Variable Abiotic Conditions in Strawberry Agroecosystems. J. Nat. Pestic. Res. 2025, 14, 100153. [Google Scholar] [CrossRef]
- Riaz, M.; Kafle, L.N.; Chang, T.; Chen, W. Characterization and Virulence of Metarhizium anisopliae (Hypocreales: Clavicipitaceae) Isolates from Ecologically Distinct Soils Against Spodoptera litura (Lepidoptera: Noctuidae). J. Insect Sci. 2026, 26, ieaf113. [Google Scholar] [CrossRef]
- Shravani, V.; Govindasamy, J.; Shanthi, A.; Johnson, I.; Nallusamy, S.; Eswaran, K.; Venkatesan, P. One Fungus, Two Foes: Clonostachys rosea as a Biocontrol Agent against Root-Knot Nematode, Meloidogyne incognita and Fusarium Wilt Disease Complex in Ridge Gourd. Arch. Microbiol. 2025, 207, 209. [Google Scholar] [CrossRef] [PubMed]
- El-Qurashi, M.A.; Almasrahi, A.A.; al-Yahya, F.A. Biological Control of Root-Knot Nematodes, Meloidogyne javanica by Antagonistic Fungus Cladosporium sphaerospermum. Plant Pathol. J. 2025, 41, 643–655. [Google Scholar] [CrossRef]
- Ramos, Y.G.; Pineda-Guillermo, S.; Tamez-Guerra, P.; Valle-Mora, J.F.; Figueroa-de la Rosa, J.I.; Ramos-Ortiz, S.; Palma-Castillo, L.J.; Martínez-Castillo, A.M. Biocontrol of Fall Armyworm Larvae by Selected Mexican Metarhizium rileyi Isolates Under Greenhouse and Small-Scale Field Conditions in Maize. Insects 2025, 16, 706. [Google Scholar] [CrossRef]
- Grossi Vanacore, M.F.; Sartori, M.V.; Giordanino, F.; Barros, G.G.; García, D. Dual Role of Bacillus velezensis EM-A8 in Maize: Biocontrol of Exserohilum turcicum and Enhancement of Plant Growth. Plants 2025, 14, 3464. [Google Scholar] [CrossRef]
- Elhalag, K.M.A.; Hassan, M.G.; Hamed, A.A.; Elawady, M.E.; Hassan, A.; El Maaty, S.A.A. Antibacterial Efficacy of Streptomyces rochei Metabolites against Key Bacterial Diseases of Potato. Indian Phytopathol. 2025, 78, 713–724. [Google Scholar] [CrossRef]
- Yamada, M.; Ramos, G.S.; Araújo, A.S.; Thiesen, L.V.; Iost-Filho, F.H.; Yamamoto, P.T. Dynamics of Tetranychus urticae Koch (Acari: Tetranychidae) in the Presence of the Predatory Mite Neoseiulus californicus (McGregor) (Acari: Phytoseiidae) in Cotton Under Semi-Field Conditions. Neotrop. Entomol. 2025, 54, 65. [Google Scholar] [CrossRef] [PubMed]
- Saleh, A.A.; Jabbar, A.S.; Anter, M.A.; Arafa, E.M.; Zawrah, M.F. Bioefficacy of Some Insecticides and Biopesticides Against Aphis gossypii Glover and Its Predator, Chrysoperla carnea (Steph.), in Cucumber Greenhouses. J. Crop Health 2025, 77, 190. [Google Scholar] [CrossRef]
- Ezahidi, B.; Amir, S.; Sabour-Alaoui, S. Essential Oils of Lavandula angustifolia and Thymus vulgaris as Biocontrol Agents: Managing Dactylopius opuntiae Infestation and Associated Bacterial Infections. Sci. Rep. 2025, 15, 34158. [Google Scholar] [CrossRef]
- Jayapradha, J.; Suganthy, M.; Murugan, M.; Janaki, P.; Rajkishore, S.K.; Sharmila, D.J.S. Silica-Mediated Resistance in Cauliflower against Diamondback Moth (Plutella xylostella). Plant Sci. Today 2025, 12, 1–8. [Google Scholar] [CrossRef]
- Roberts, N.S.; Ndayiragije, J.C.; Özek, T.; Butt, T.M.; Karaca, I.; Shah, F.A.; Allen, W.L. Visual Modelling Can Optimise Sticky Trap Design for Simultaneous Monitoring of Multiple Species of Insect Pests. Sci. Rep. 2025, 15, 17280. [Google Scholar] [CrossRef] [PubMed]
- Ansari-Shiri, H.; Hajiqanbar, H.; Zalucki, M.P.; Fathipour, Y. Assessing Population Growth Potential of Phytonemus pallidus (Acari: Tarsonemidae) on Different Strawberry Cultivars Using Group-Rearing Life Table. Syst. Appl. Acarol. 2025, 30, 1223–1232. [Google Scholar] [CrossRef]
- Sabet, H.; Asadi-Gharneh, H.A.; Nasr- Esfahani, M. Butternut Pumpkin-Powdery Mildew Disease Interaction as Influenced by Sowing Type and Date. Ecol. Genet. Genom. 2025, 36, 100375. [Google Scholar] [CrossRef]
- Nouri-Miri, M.; Kheradmand, K.; Saboori, A.; Fathipour, Y. Age-Gender-Specific Functional and Age-Specific Numerical Responses of Neoseiulus californicus (Acari: Phytoseiidae) on Two-Spotted Spider Mite. Exp. Appl. Acarol. 2025, 94, 5. [Google Scholar] [CrossRef]




| PICOS Component | Inclusion Criteria | Exclusion Criteria |
|---|---|---|
| Population (P) | Crops (vegetables, small fruits, and herbs) grown under protected greenhouses located specifically in the Global South. | Open-field cultivation, forestry systems, or crops grown in the Global North. Studies on stored product pests or vectors of human diseases. |
| Intervention (I) | Sustainable pest management strategies, including biological control, cultural practices, physical barriers, botanical extracts, semiochemicals, and Integrated Pest Management programs. | Strategies that rely exclusively on synthetic chemical pesticides, without an IPM component or validation of sustainable alternatives, or GMOs. |
| Comparison (C) | Studies that include a control group (untreated check), a conventional chemical control group, or a comparison of different sustainable management strategies. | Descriptive studies lack a control group or comparative statistical analysis. |
| Outcome (O) | Quantitative data on pest population reduction, crop damage mitigation, yield impact, or economic viability of the strategy. | Studies reporting only qualitative observations, preliminary in vitro results without greenhouse validation, or non-target effects only. |
| Study Design (S) | Original peer-reviewed research articles presenting primary empirical data. | Reviews, meta-analyses, conference abstracts, book chapters, editorials, and gray literature. |
| Additional Limits | Articles published in English or Spanish between 2017 and 2024. | Articles in other languages or published outside the defined timeframe. |
| Control Strategy | Records | Sub-Type | Records | Species | Records | Source | |
|---|---|---|---|---|---|---|---|
| Biological | 101 | 54.3% | Fungi | 36 | Beauveria sp. | 8 | [20,21,22,23,24,25,26,27] |
| Trichoderma sp. | 7 | [28,29,30,31,32,33,34] | |||||
| Metarhizium sp. | 5 | [3,22,23,24,35] | |||||
| Pochonia sp. | 3 | [21,36,37] | |||||
| Lecanicillium sp. | 3 | [20,27,38] | |||||
| Aspergillus sp. | 2 | [30,36] | |||||
| Glomus sp. | 1 | [39] | |||||
| Penicillium sp. | 1 | [36] | |||||
| Purpureocillium sp. | 1 | [40] | |||||
| Others | 5 | [31,41,42,43,44] | |||||
| Bacteria | 17 | Bacillus sp. | 7 | [21,22,28,29,45,46,47] | |||
| Pseudomonas sp. | 4 | [32,33,40,48] | |||||
| Kluyvera ascorbata | 2 | [46,49] | |||||
| Azospirillium brasilense | 1 | [45] | |||||
| Azotobacter chroococcum | 1 | [45] | |||||
| Paecilomyces formosus | 1 | [50] | |||||
| Paenibacillus sp. | 1 | [51] | |||||
| Nematodes | 13 | Steinernema sp. | 7 | [22,52,53,54,55,56,57] | |||
| Heterorhabditis bacteriophora | 6 | [22,52,54,55,56,57] | |||||
| Parasitoids | 10 | Encarsia formosa | 3 | [58,59,60] | |||
| Trichograma sp. | 3 | [61,62,63] | |||||
| Eretmocerus eremicus | 1 | [64] | |||||
| Tamarixia triozae | 1 | [64] | |||||
| Stenomesius sp. | 1 | [65] | |||||
| Bracon nigricans | 1 | [65] | |||||
| Entomophagous insects | 8 | Orius laevigatus | 2 | [66,67] | |||
| Dicyphus hesperus | 2 | [64,68] | |||||
| Chrysopa pallens | 1 | [69] | |||||
| Macrolophus pygmaeus | 1 | [9] | |||||
| Apanteles gelechiidivoris | 1 | [70] | |||||
| Eriopis connexa. | 1 | [71] | |||||
| Predatory mites | 4 | Amblyseius swirskii | 2 | [72,73] | |||
| Phytoseiulus persimilis | 1 | [74] | |||||
| Neoseiulus cucumeris | 1 | [72] | |||||
| Virus | 3 | Nucleopolyhedrovirus (NPV) | 3 | [35,75,76] | |||
| Extracts and chemical compounds | 51 | 27.4% | Plant extracts | 39 | [32,33,38,39,40,47,48,59,60,73,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105] | ||
| Pheromones | 7 | [60,70,106,107,108,109,110] | |||||
| Bacteria metabolites | 3 | [102,106,111] | |||||
| Mineral oils | 2 | [74,112] | |||||
| Other strategies | 22 | 11.8% | Color traps | 5 | [60,106,107,113,114] | ||
| Plant residues Incorporation | 4 | [37,47,115,116] | |||||
| Resistance induction | 2 | [117,118] | |||||
| Nanoparticles | 2 | [119,120] | |||||
| Light traps | 2 | [60,121] | |||||
| Variety evaluation | 2 | [9,118] | |||||
| Mating techniques | 2 | [109,122] | |||||
| Math algorithms | 2 | [123,124] | |||||
| Population distribution | 1 | [125] | |||||
| Cultural practices | 12 | 6.5% | Functional biodiversity | 5 | [126,127,128,129,130] | ||
| Climate management | 4 | [26,131,132,133] | |||||
| Nutritional management | 2 | [87,134] | |||||
| Population management | 1 | [135] | |||||
| Control Strategy | Subtype | Agent/Target | Quantitative Efficacy Data | Application Method/ Mechanism of Action | Application Limitations | Source |
|---|---|---|---|---|---|---|
| Biological Control | Fungi | Metarhizium rileyi vs. Spodoptera frugiperda | 88% to 96% mortality in greenhouse trials. | The application of virulent isolates aimed at the whorls produces effective control. | Conventional spraying is ineffective. | [3] |
| Beauveria bassiana (strains ATCC and R444) vs. T. urticae | >92.86% reduction in eggs 95.1–99.4% in mobile forms. | It affects female fertility and has adverse effects on other biological parameters. | It should be applied in the early stages of infestation. | [20] | ||
| Fungi (interaction) | Penicillium chrysogenum + Pochonia chlamydosporia (Culture filtrates) vs. Meloidogyne incognita | ~100% egg hatch inhibition after 72 h. | Synergistic effect. Direct parasitism or the release of toxic metabolites. | Incompatibility between some control agents. | [36] | |
| Bacteria + fungi (interaction) | Bacillus thuringiensis (GP139) + B. bassiana (HPI-019/14) vs. Bemisia tabaci | >90% mortality against nymphs at high spore concentrations. | Additive effect. Persistent activity against different stages. | The insect molting process can eliminate the infectious fungal inoculum. | [21] | |
| Bacteria | Bacillus subtilis, Azospirilum brasilense and Azotobacter chroococcum vs. M. incognita | Egg mass reduction: B. subtilis: 95.4%. A. brasilense: 90.9%. A. chroococcum: 90.9%. | Different mechanisms: Some of them are products with bioactive substances that directly affect the nematode’s egg hatching and mobility. | Influenced by soil biota and host plant factors. | [45] | |
| B. thuringiensis subsp. kurstaki (Btk) vs. T. absoluta. | 78–91% reduction in population. | Suspension concentrate is more effective than wettable powder. Cry toxins bind to midgut receptors, causing pore formation and lysis of the gut epithelium. | Not effective against 4th instar larvae; degrades quickly under UV light. | [102] | ||
| Insect | Apanteles gelechiidivoris vs. T. absoluta | 86.38% maximum parasitism of susceptible larvae. | Larval endoparasitism; higher efficacy when combined with pheromones. | Susceptible to non-selective insecticides. | [70] | |
| Nematode + bacteria | Six nematodes species (Steinernema sp. + Heterorhabditis bacteriophora) + Xenorhabdus spp. and Photorhabdus spp. vs. T. absoluta | 80% to 100% larval mortality. | Synergistic effect with mutualistic bacteria. Nematodes penetrate the insect’s body through the mouth, anus, cuticle, or spiracles. Bacteria cause septicemia. | High susceptibility to desiccation and UV light. | [52] | |
| Nematode + fungi | H. bacteriophora + B. bassiana vs. Thrips tabaci | 94.73% pre-pupae mortality. 82.45% pupae mortality | Additive and synergistic effects. Fungi infect insects by attaching their conidia to the insect’s cuticle. Nematodes penetrate the insect’s body through the mouth, anus, cuticle, or spiracles. | Restricted by soil moisture and temperature; requires soil-dwelling life stages of the pest. | [22] | |
| H. bacteriophora + Metarhizium anisopliae vs. T. tabaci | 85.96% pre-pupae mortality. | |||||
| Steinernema feltiae + B. bassiana vs. T. tabaci | 81.57% pre-pupae mortality. 90.43% pupae mortality. | |||||
| Extracts and Compounds | Essential oil | Clove (CO), peppermint oil (PO) and basil (BO) vs. T. urticae | CO (24 h): Adult mortality 100% and immatures mortality >80% at concentrations ≥200 µLL−1 Air. PO (24 h): Adult mortality 88.6% and immatures mortality 82.2% at concentrations 400 µLL−1 Air. BO: Adult mortality 80.4% (48 h) and immatures mortality 84.6% (72 h) at concentrations 400 µLL−1 Air. | Spray application. Additive effect, as essential oils have different phenylpropanoids and monoterpenes with a wide range of mechanisms of action. | High concentrations may cause phytotoxicity to sensitive greenhouse crops. | [104] |
| Natural compound | Chitosan vs. M. incognita | 81.4% reduction in root galls. 90.9% reduction in egg mass. | Induces local/systemic resistance trough elicitation of phytoalexins, lignin, callose and other compounds. | Time-dependent. | [45] | |
| Plant extract | Azadirachtin vs. T. absoluta | 70–83% reduction in population. | Antifeedant and repellent effects. | Incompatibility with control by entomophagous insects. | [102] | |
| Bacteria metabolite | Spinosad vs. T. absoluta | 78–97% reduction in population. | Disrupts insect nervous system, leading to paralysis and death. | High risk of resistance development in field populations. | ||
| Pheromones | Synthetic sex pheromones (Isonet®T) vs. T. absoluta | 87.23% male reduction. 85.97% egg reduction. | Pheromone dispenser. Mating disruption. | High cost. | [109] | |
| Other Strategies | Math algorithm | LOSS Algorithm (Machine Vision) vs. B. tabaci | High correlation indexes in comparison with other counting methods: sticky screens (R2 = 0.97) and plant leaf images (R2 = 1.0). | Sensing the insect presence using hunting traps. | High hardware costs; and technical expertise are required. | [123,124] |
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© 2026 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Share and Cite
Ubaque, H.; Hincapié, C.A.; Osorio, M. Sustainable Pest Management Strategies Under Greenhouse Conditions in Countries of the Global South. Horticulturae 2026, 12, 273. https://doi.org/10.3390/horticulturae12030273
Ubaque H, Hincapié CA, Osorio M. Sustainable Pest Management Strategies Under Greenhouse Conditions in Countries of the Global South. Horticulturae. 2026; 12(3):273. https://doi.org/10.3390/horticulturae12030273
Chicago/Turabian StyleUbaque, Harold, Carlos A. Hincapié, and Marisol Osorio. 2026. "Sustainable Pest Management Strategies Under Greenhouse Conditions in Countries of the Global South" Horticulturae 12, no. 3: 273. https://doi.org/10.3390/horticulturae12030273
APA StyleUbaque, H., Hincapié, C. A., & Osorio, M. (2026). Sustainable Pest Management Strategies Under Greenhouse Conditions in Countries of the Global South. Horticulturae, 12(3), 273. https://doi.org/10.3390/horticulturae12030273

