119 Dohouonan et al. Int. J. Biosci. 202 5 RESEARCH PAPER RESEARCH PAPERRESEARCH PAPER RESEARCH PAPER OPEN ACCESS OPEN ACCESSOPEN ACCESS OPEN ACCESS Diversity and abundance of insects found on okra Abelmonchus esculentus cultivation in Man, Côte d’Ivoire Diabate Dohouonan *1 , Coulibaly Tenon 2 , N’guessan Ehikpa Naomie Melinand 3 , Tano Yao 4 1 Department of Agronomy and Forestry, University of Man, Côte d’Ivoire 2Department of Animal Biology, Universit Péléforo Gon Coulibaly, Korhogo, Côte d’Ivoire 3Department of Sciences and Techniques, University Alassane Ouattara, Bouaké, Côte d’Ivoire 4University Nangui Abrogoua, Abidjan, Côte d’Ivoire Key words: Abelmonchus esculentus , Amrasca biguttula , Brachymyrmex patagonicus , Auxiliary insects, Insect pests http://dx.doi.org/10.12692/ijb/26.1.119-125 Article published on January 05, 2025 Abstract Abelmonchus esculentus is an important source of vitamins and minerals. However, okra plants were damaged by insect pests. This study carried out to evaluate the diversity of insects on okra plants in Man locality, for better pest management. Insects were recorded from 21 th to 70 th Day After Sowing, on Clemson spineless okra sown on March 2 nd , 2024. A total of 12 species belonging to 6 orders (Hymenoptera, Hemiptera, Orthoptera, Diptera, Lepidoptera, Coleoptera) were collected. The relative abundances of insect pests, predators, parasitoids and pollinators were 55.13%, 17.95%, 7.26% and 19.66% respectively during the vegetative phase, and 69.34%, 17.33%, 5.78% and 7.55% during the reproductive phase, respectively. The Hemiptera Amrasca biguttula, Podagrica decolorata, Dysdercus voelkeri, Bemisia tabaci, Lepidoptera Plutella xylostella and, Orthopterans Oecanthus fultonis, Locusta migratoria and Criotettix bispinosus are pests. Sarcophaga sp (Diptera) is a parasitoid and Brachymyrmex patagonicus (Hymenoptera) is a pollinators. The Coleoptera Coccinella septempunctata, Coccinella cheilomenes and Alticini sp are predators. During the vegetative stage, B. patagonicus (42.09%) and A. biguttula (29.93%) were the most abundant. During the reproductive stage, the highest number of A. biguttula (47.6%), P. decolorata (15.13%), D. voelkeri (13.57%) and B. patagonicus (11.59%) were recorded. Shannon and Margalef indices were higher during the reproductive stage (1.645, 1.602) than those of the vegetative stage (1.589, 1.477). The equitability indices are similar (0.66) for both phases. Knowledge of okra entomofauna will help for integrated pest management. * Corresponding Author: Diabate Dohouonan
[email protected] International Journal of Biosciences | IJB | ISSN: 2220-6655 (Print) 2222-5234 (Online) http://www.innspub.net Vol. 26, No. 1, p. 119-125, 2025
120 Dohouonan et al. Int. J. Biosci. 202 5 Introduction Okra Abelmonchus esculentus accounts for around 1.5% of total vegetable production worldwide (Sathish et al., 2013). It is rich in protein, vitamins and minerals (Krishna et al., 2022). In West Africa, this crop ranks second after tomatoes (Birlouez, 2020). In Côte d'Ivoire, A. esculentus production is estimated at 185,800 tonnes per year (Soro et al., 2016). This crop supplements the population's nutritional needs, which consist exclusively of carbohydrates (Diabaté, 2016). The fruit is rich in calcium, iron, carbohydrates, proteins and vitamins (Khomsug et al., 2010). It is widely consumed in Côte d'Ivoire, particularly in the Tonkpi region. In the Tonkpi region, all parts of the okra except the roots are consumed. It is therefore of vital importance to the people of this region. Okra is also used in traditional medicine and industry (Marius et al., 1997). However, okra is attacked by a large number of insect pests, which limit its production. On the other hand, this crop is home to auxiliary insects that help pollinate the plant and limit the outbreak of insect pests. Insect pests consume okra leaves and leave holes in them, resulting in reduced photosynthesis and lower yields (Soro et al., 2016; Diabaté et al., 2024). These insects also attack okra fruits, reducing their market value and negatively influencing food security (AsareBediako et al., 2014 ; Birlouez, 2020 ; Zhussip et al., 2024). Biting-sucking insects, in particular Amrasca biguttula, Bemisia tabaci and Aphis gossypii, are major pests of okra and are responsible for over 17% of yield loss (Mandal et al., 2006; Sarkar et al., 2015). To increase okra yields, farmers use pesticides whose doses and application times are not respected. This has led to the emergence of insect resistance to a wide range of insecticides (Srinivas et al., 2004; Diabaté, 2016; Bade and Bhamare, 2023). Pest management requires a good knowledge of the organisms for targeted control. The general objective of this study was to assess the diversity of insects infested with the okra crop established in the locality of Man, for better pest management. The aim is to determine the insects that are present on okra during the vegetative and reproductive phases. Materials and methods Study site Okra, Clemson spineless variety was sown on March 2, 2024, in stacks over a quarter-hectare in the entomological plot at the University of Man (7°21'09''N and 7°36'57''W), in the Tonkpi region, west of Côte d'Ivoire. Three seeds were sown in clusters with a distance of 60 cm between rows and 60 cm between plants. After germination, the plants were separated to obtain two plants per cluster. The plot was weeded as required. The climate of this region is tropical, with one dry and one rainy seasons. The average annual temperature and rainfall were 25.0°C and 1,632 mm, respectively. Ferralitic soils of average chemical fertility were predominant (Tiessé, 2020). Insect sampling, conservation and identification The insects were recorded on okra plants from the 21 st to the 70 th day after grains sowing, from 6 a.m. to 11 a.m. weekly on 12 plants per elementary plot. During each observation, the lower and upper of the leaves were checked for the presence or absence of insect pests. Insect larvae were captured using flexible forceps. The numbers of each species were recorded. Specimens of each insect species were then preserved in small plastic jars containing 70% alcohol. Insects were identified on the basis of family recognition keys (Roth, 1974; Delvare and Aberleng, 1989). Relative abundance (AR) and frequency of occurrence (FO) of insects on okra plants The relative abundance (RA) of insects on okra plants were calculated according to the following formula: ܣܴ (%) = ∗ ଵ (1) Where, n = total number of individuals collected for a given species; N= total number of individuals collected. The occurrence frequency (Fo) of insects on okra plants were calculated using the following formula: ܨ(%) = ∗ ଵ (2)
121 Dohouonan et al. Int. J. Biosci. 202 5 Where, a = Number of plants sampled with the given insect; A = Total number of plants sampled. The species were then classified according to its frequency of occurrence. It is said to be rare (Fo < 5%), incidental (5% ≤ Fo < 25%), frequent (25% ≤ Fo <50%), constant (50% ≤ Fo < 100%) or ubiquitous (Fo = 100%) (Dajoz, 2006; Akpesse et al., 2022). Determination of species richness and diversity Specific richness (S), which is the total number of insect species collected in okra fields, is determined. Biological diversity indices were evaluated by calculating the Shannon (H'), Margalef and equitability indices. Shannon diversity index The Shannon index (H’) simultaneously takes into account the specific richness and abundance of the different insect families found on a plot. This index is calculated according to the following formula: Shannon diversity index (H')= - Σ pi ln pi (3) Where: pi = probability of encountering family i, pi=ni/N ; ni = abundance of species i, and N = total abundance. Margalef index The Margalef index is used to determine insect diversity at a given site. It is calculated according to the following formula : d = (ୗିଵ) ୪୬ (5) Where: N = total number of individuals of a species and S = species richness. Equitability index The equitability index (E) was used to determine the equitable distribution of individuals. Its aim was to observe the equilibrium of the populations. This index was determined according to the following formula: ܧ = ୌᇱ ୪୬ ௌ (4) with : H' = Shannon Diversity Index, and S = Species Richness. The value of E varies from 0 (dominance of one species) to 1 (equitable distribution of individuals). Statistical analysis The number of insects collected on okra plants was subjected to an analysis of variance (ANOVA main effects, p < 5%) using SPSS Statistic version 20 software. The means were discriminated using XLSTAT 2016 software (Fisher LSD test, p < 5%). Shannon, equitability and Margalef indices were determined using Estimate version 22.0 software (IBM, New York, USA). Results Insects diversity on okra plants A total of 11 insect species with 872 individuals were observed during the vegetative phase and 12 species with 958 individuals during the reproductive phase. The Shannon index is greater than 1.5 during the vegetative and reproductive phases of okra. It is higher during the reproductive stage, with a value of 1.65, than during the vegetative stage (1.59). This insect diversity is confirmed by the Margalef index, which showed a higher value (1.60) during the reproductive stage than during the vegetative stage (1.48). The equitability indices obtained during the vegetative and reproductive stages are equal to 0.66. These values, close to 0.5, show that there is no equitable distribution of okra-infested insects (Table 1). Table 1. Biodiversity index for okra insects Diversity indices Vegetative stage Reproductive stage Individuals 872 958 Taxa_S 11 12 Shannon_H 1. 59 1. 65 Margalef 1. 48 1. 60 Equitability_J 0. 66 0. 66 Frequency of occurrence of okra insects In the course of this study, 6 insect orders were sampled. These were the orders Hymenoptera, Hemiptera, Orthoptera, Diptera, Lepidoptera and Coleoptera. Lepidoptera were rare (Fo < 5%),
122 Dohouonan et al. Int. J. Biosci. 202 5 Diptera and Orthoptera were accessory (5% ≤ Fo < 25%), and Coleoptera and Hemiptera were frequent (25% ≤ Fo <50%) on okra plants. Their frequencies of occurrence were respectively 35.04% and 38.67% for Coleoptera, 3.85% and 3.11% for Lepidoptera, 7.26% and 5.75% for Diptera, 12.36% and 12% for Orthoptera and 21.8% and 32.89% for Hemiptera during the vegetative and reproductive stages (Fig. 1A). Fig. 1. Occurrence frequencies of insect orders (A) and their functions (B) recorded on okra plant The insects collected were grouped into 4 categories: pests, predators, parasitoids and pollinators. The frequencies of insect pests, predators, parasitoids and pollinators are 55.13%, 17.95%, 7.26% and 19.66% respectively during the vegetative phase, and 69.34%, 17.33%, 5.78% and 7.55% during the reproductive phase (Fig. 1B). The insects Amrasca biguttula (Hemiptera: Cicadellidae) (Fig. 2a), Podagrica decolorata (Hemiptera: Chrysomelidae) (Fig. 2b), Dysdercus voelkeri (Hemiptera: Pyrrhocoridae) (Figs 2c,d), Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), Plutella xylostella L. (Lepidoptera: Plutellidae) (Fig. 2e), Oecanthus fultonis (Orthoptera: Gryllidae), Locusta migratoria (Ortoptera: Acrididae) and Criotettix bispinosus (Orthoptera: Tettrigidae) are pests. Hemipterans attached to okra are sucking, biting insects. They sting leaves and stems and inject viruses, resulting in loss of raw and processed sap, reduced photosynthesis, disease outbreaks and lower yields. Sarcophaga sp (Diptera: Sarcophagidae) is a parasitoid and Brachymyrmex patagonicus (Hymenoptera: Formicidae) is a pollinator (Fig. 2f). In addition, Coccinella septempunctata (Coleoptera: Coccinellidae), Coccinella cheilomenes (Coleoptera: Coccinellidae) (Fig. 2g) and Alticini sp (Coleopera: Chrysomelidae) (Fig. 2h) are predators. Parasitoids, predators and pollinators help increase okra yields. Parasitoids and predators attack insect pests, reducing their numbers and attacks. Fig. 2. Some insects associated with okra plant (a : Amrasca biguttula , b : Podagrica decolorata , c & d : Dysdercus voelkeri, e : larve de Plutella xylostella, f : Brachymyrmex patagonicus, g : Coccinella cheilomenes, h : Alticini sp).
123 Dohouonan et al. Int. J. Biosci. 202 5 Table 2. Relative abundance and insects collected functions in the okra plants during the vegetative and reproductive phases Insects recorded Insect status Vegetative phase Reproductive phase N AR (%) N AR (%) Podagrica decolorata R 20 ± 2. 82 c 9. 18 36.25 ± 9. 25 b 15 . 13 Coccinella septempunctata Pre 5.50 ± 1. 73 d 2. 52 4.75 ± 0. 95 c 1 . 98 Coccinella cheilomenes Pre 17.75 ± 3. 94 c 8. 14 1 . 75 ± 0 . 5 c 0 . 73 Plutella xylostella R 2.25 ± 0. 95 d 1. 03 1 . 75 ± 0 . 5 c 0 . 73 Sarcophaga sp Par 4 ± 2. 58 d 1. 83 3 . 75 ± 2 . 21 c 1 . 57 Oecanthus fultonis R 3 ± 1. 41 d 1. 38 3 ± 1 . 15 c 1 . 25 Locusta migratoria R 1.75 ± 0. 95 d 0. 8 1 . 75 ± 0 . 95 c 0 . 73 Criotettix bispinosus R 3 ± 2. 30 d 1. 38 2 . 75 ± 1 . 70 c 1 . 15 Brachymyrmex patagonicus P 91.75 ± 12. 68 a 42. 09 27 . 75 ± 14 . 38 b 11 . 59 Amrasca biguttula R 65.25 ± 12. 8 b 29. 93 114 ± 22 . 46 a 47 . 6 Dysdercus voelkeri R 0 ± 0 d 0 32 . 50 ± 14 . 79 b 13 . 57 Alticini sp R 0 ± 0 d 0 9 . 50 ± 5 . 26 c 3. 97 Bemisia tabaci R 3.75 ± 2. 21 d 1. 72 0 ± 0 c 0 F 118. 495 - 48 . 767 - p 0. 000 - 0 . 000 - AR = relative abundance, N = number of insects recorded, P = pollinators, Par = parasitoids, Pre = predators, R= pests. Means with the same letter in the same column do not differ statistically from each other (Fisher LSD test, p < 0.05). Relative abundance of insects associated with okra cultivation The Coleoptera species C. septempunctata, C. cheilomenes and Alticini sp, the Lepidoptera P. xylostella, the Diptera Sarcophaga sp, the Orthoptera O. fultonis, L. migratoria, C. bispinosus, the Hymenoptera B. patagonicus and the Hemiptera A. biguttula, P. decolorata, D. voelkeri, and B. tabaci were collected from okra plants. The Hemipterans D. voelkeri and the Coleoptera Alticini sp were not observed during the vegetative stage. During the reproductive phase, B. tabaci was not observed. Then, during the vegetative stage, B. patagonicus and A. biguttula were the most abundant, with frequencies of 42.09% (91.75 individuals) and 29.93% (65.25 individuals), respectively. They were followed by P. decolorata (9.18% or 20 individuals), C. cheilomenes (8.14% or 17.75 individuals), C. septempunctata (2.52% or 5.5 individuals), Sarcophaga sp (1.83% or 4 individuals), B. tabaci (1.72% or 3.75 individuals), O. fultonis (1.38% or 3 individuals), C. bispinosus (1.38% or 3 individuals), P. xylostella (1.03% or 2.25 individuals), L. migratoria (0.8% or 1.75 individuals) (F = 118. 495; p = 0.000). During the breeding stage, A. biguttula, P. decolorata, D. voelkeri and B. patagonicus were the most abundant, with frequencies of 47.6%, 15.13%, 13.57% and 11.59%, respectively. The insects Alticini sp. (3.97%), C. septempunctata (1.98%), Sarcophaga sp (1.57%), O. fultonis (1.25%) and C. bispinosus (1.15%) were sparsely observed on okra plants during the reproductive stage. The numbers of C. cheilomenes, P. xylostella and L. migratoria were very low, below 1% on the plants. Their frequencies are identical and equal to 0.73%, i.e. 1.75 insects (F = 48.767; p = 0.000) (Table 2). Discussion The insects collected on okra plants belong to 6 orders which were the orders of Hymenoptera, Hemiptera, Orthoptera, Diptera, Lepidoptera and Coleoptera. In the vegetative phase 872 insects were recorded from 11 insect species, while the reproductive phase 958 individuals were recorded from 12 species. Similar results were obtained by Boateng et al. (2019) in Ghana. According to these authors, the orders Coleoptera, Hemiptera, Lepidoptera, Hymenoptera, Orthoptera and Mantodea are all related to okra cultivation. In addition, the families Coccinellidae, Cicadellidae, Formicidae, Chrysomelidae, Aleyrodidae and Acrididae were the most abundant. These insects belong to the pest, parasitoid, predator and pollinator groups. The insect pest A. biguttula was
124 Dohouonan et al. Int. J. Biosci. 202 5 the most numerous during the vegetative and reproductive phases. These results are in line with those of Challa et al. (2020), who showed that jassid numbers ranged from 3.5 jassids/6 leaves on day 44 after sowing to 4 jassids/leaf on day 47 after sowing. The four Hemiptera A. biguttula, P. decolorata, D. voelkeri and B. tabaci are insect pests of okra. A. biguttula, D. voelkeri and B. tabaci are sucking biters. They bite the leaves and stems of plants and inject disease-causing viruses (Ugwoke and Onyishi, 2009; Ojiako et al., 2018; Krishna et al., 2022). P. decolorata and orthopterans consume okra leaves, reducing leaf area and lowering yield (Ugwoke and Onyishi, 2009; Soro et al., 2016; Diabaté et al., 2024). Work by Mandal et al. (2006), Sarkar et al. (2015) and Ojiako et al. (2018) has shown that Podagrica spp., Dysdercus spp. and B. tabaci are the major insect pests that infest leaves and considerably reduce yield. Yield losses can reach 18%. Orthopterans sometimes cut young plants, reducing plant density. These defoliating insects destroy the plant and cause its death (Zhussip et al., 2024). According to Krishna et al. (2022), these insect pests are responsible for major yield losses in okra. Conclusion Six insect orders comprising 12 species were collected from okra plants. These were Hymenoptera (B. patagonicus), Hemiptera (A. biguttula, P. decolorata, D. voelkeri, B. tabaci), Orthoptera (O. fultonis, L. migratoria and C. bispinosus), Diptera (Sarcophaga sp.), Lepidoptera (P. xylostella) and Coleoptera (C. septempunctata, C. cheilomenes and Alticini sp.). The insects collected were divided into four groups: pests, predators, parasitoids and pollinators. During the vegetative stage, B. patagonicus and A. biguttula were the most abundant. During the reproductive stage, A. biguttula, P. decolorata, D. voelkeri and B. patagonicus were the most numerous. The Shannon and Margalef indices are 1.65 and 1.60 during the breeding stage and 1.59 and 1.48 during the vegetative stage. Equitability indices were equal to 0.66 for both phases. References Akpesse AAM, Diabaté D, Coulibaly T, Kouadja YO, Koua KH, Kouassi KP. 2022. Termitic diversity of the Dalhia Fleurs partial natural reserve (Bingerville, Côte d’Ivoire). Journal of Agricultural and Ecology Research International 23(6), 82–92. DOI: 10.9734/JAERI/2022/v23i6501. Bade AS, Bhamare VK. 2023. Insecticidal resistance in Helicoverpa armigera (Hübner) infesting chickpea. Indian Journal of Entomology, 1– 4. DOI: 10.55446/IJE.2023.1348. Birlouez E. 2020. Petite et grande histoire des légumes. Editions Quæ, Paris (France), 170p. Boateng F, Amiteye S, Appiah AS, Marri D, Offei BK, Ofori SEK, Amoatey H. 2019. Insect pest diversity and damage assessment in field grown okra (Abelmoschus esculentus (L.) Moench) in the coastal savannah agro-ecological zone of Ghana. Journal of Agriculture and Ecology Research International 18(4), 1–10. Challa M, Sharma AK, Saxena AK, Mishra YK, Rathore J. 2020. Population dynamics of major insects of okra in relation to weather parameters in Jabalpur District of Madhya Pradesh. International Journal of Current Microbiology and Applied Sciences 11, 2082–2088. Dajoz R. 2006. Précis d’écologie, 8è Edition, Ed. Dunod, Paris, France, 631p. Delvare G, Aberleng P. 1989. Les Insectes d’Afrique et d’Amérique Tropicale. Clé pour la reconnaissance des familles. Laboratoire de faunistique, Département GERDAT: Montpellier, France, 194p. Diabaté D, N’Guessan ENM, Coulibaly T, Tano Y. 2024. Diversity of Coleoptera on cucumber in the Tonkpi region of Man, Côte d’Ivoire. Indian Journal of Entomology 86(2), 351–355. DOI: 10.55446/IJE.2024.1692.
125 Dohouonan et al. Int. J. Biosci. 202 5 Diabaté D. 2016. Impact et mode d’action de quelques biopesticides et insecticides classiques en culture maraîchère dans la région du Moronou (Bongouanou, Côte d’Ivoire). Thèse unique de Doctorat, Université Félix Houphouët-Boigny, Côte d’Ivoire, 148p. Khomsug P, Thongjaroenbuangam W, Pakdeenarong N, Suttajit M, Chantiratikul P. 2010. Antioxidative activities and phenolic content of extracts from okra (Abelmoschus esculentus L.). Research Journal of Biological Sciences 5, 310–313. Krishna B, Kumar R, Choudhary JS, Kumar R, Hans H. 2022. Insect pests in okra agro-ecosystem and their integrated management. Indian Horticulture, 30–34. Mandal SK, Sah SB, Gupta SC. 2006. Efficacy and economics of biopesticide and insecticide combinations against okra pests. International Journal of Agricultural Science 2(2), 377–380. Marius C, Gerard V, Antoine G. 1997. Le gombo, Abelmoschus esculentus (L.) Moench une source possible de phospholipides. Agronomie et Biotechnologies, Oléagineux, Corps Gras, Lipides 4(5), 389–392. Ojiako FO, Ibe AE, Ogu EC, Okonkwo CC. 2018. Effect of varieties and mulch on foliar insect pests of okra (Abelmoschus esculentus L. (Moench)) in a humid tropical environment. Agrosearch 18(2), 38– 58. https://dx.doi.org/10.4314/agrosh.v18i2.4. Roth M. 1974. Initiation à la morphologie, la systématique et la biologie des insectes. Editions de l’office de la recherche scientifique outre-mer, Paris, France, 212p. Sarkar S, Patra S, Samanta A. 2015. Evaluation of bio-pesticides against red cotton bug and fruit borer of okra. The Bioscan 10(2), 601–604. Sathish KD, Eswar TD, Praveen KA, Ashok KK, Bramha SRD, Ramarao N. 2013. A review on Abelmoschus esculentus (Okra). International Research Journal of Pharmaceutical and Applied Sciences 3(4), 129–132. Soro S, Yéboué NL, Tra BCS, Zadou DA, Koné I. 2016. Dynamics of the flea beetle Podagrica decolorata Duvivier, 1892 (Insecta: Chrysomelidae) on okra crops: Implications for conservation of the Tanoe-Ehy Swamp Forests (Southeastern Ivory Coast). Journal of Animal & Plant Sciences 30, 4758– 4766. Srinivas R, Udikeri SS, Jayalakshmi SK, Sreeramulu K. 2004. Identification of factors responsible for insecticide resistance in Helicoverpa armigera. Comparative Biochemistry and Physiology Part C: Toxicology and Pharmacology 137, 261–269. Tiessé BAC. 2020. Apport de la télédétection et des SIG pour le suivi spatio-temporel de l’occupation du sol et la cartographie de la sensibilité à l’érosion hydrique dans la région montagneuse du Tonkpi (Ouest de la Côte d’Ivoire). Thèse Unique de Doctorat, Institut National Polytechnique Félix Houphouët-Boigny, Yamoussoukro, Côte d’Ivoire, 171p. Ugwoke KI, Onyishi LE. 2009. Effects of Mycorrhizae (Glomus musae), poultry manure, and okra mosaic potyvirus (OKMV) on yield of okra (Abelmoschus esculentus). Production Agriculture and Technology 5, 359–369. Zhussip M, Akhmetov K, Burkitbaeva U, Amanova G, Mazhenova L. 2024. Contribution to the diversity of leaf miners of silver birch, Betula pendula Roth in North-Eastern Kazakhstan. Journal of Insect Biodiversity and Systematics 10(3), 589–604. https://doi.org/10.61186/jibs.10.3.589.