Assessing Physicochemical and Heavy Metal Levels in Drinking Water of San Francisco, Agusan del Su | InformativeBD

Physicochemical properties and heavy metal concentrations in the drinking water of San Francisco, Agusan Del Sur, Philippines

Kevin Hope Z. Salvaña,  Romeo M. Del Rosario, and  Angelo Mark P. Walag, from the different institute of Philippines. wrote a Reseach Article about, Assessing Physicochemical and Heavy Metal Levels in Drinking Water of San Francisco, Agusan del Su. Entitled, Physicochemical properties and heavy metal concentrations in the drinking water of San Francisco, Agusan Del Sur, Philippines. This research paper published by the Journal of Biodiversity and Environmental Sciences (JBES). an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

Concerned about the safety of public drinking water supply, this study delved into the drinking water system in San Francisco, Agusan del Sur, Philippines. There were two areas of concern in this study: the physicochemical properties which include alkalinity, conductivity, pH, salinity, total dissolved solids (TDS), total hardness, total suspended solids (TSS), and turbidity; and the heavy metal contaminants which include cadmium, chromium, cobalt, copper, lead, manganese, and nickel. The physicochemical properties and chemical contaminants present in both untreated and treated water were described based on their measured levels and were evaluated using the PNSDW 2017 and WHO-GDWQ. The findings showed that there is a decrease of levels in conductivity, TSS, turbidity, and manganese after the water treatment. The levels of total hardness at 303.02 mg/L fail to conform to the PNSDW 2017 and WHO-GDWQ standards while the rest of the physicochemical properties (alkalinity, conductivity, pH, salinity, TDS, total hardness, TSS, and turbidity) are under the maximum allowable level (MAL). The levels of Cadmium, Chromium, Copper, Lead, Manganese, and Nickel are lower than the MAL value of the PNSDW 2017 and WHO-GDWQ. Manganese, which has no health-associated risk but might affect water acceptability, is measured at 0.008 mg/L and is lower than the MAL at 0.4000 mg/L in both standards. Generally, the water is not acceptable for drinking due to high levels of total hardness. Other mandatory parameters for microbiological quality are recommended to determine the suitability of the drinking water for human consumption.

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Read morePhenotypic Assessment of Six Cassava Families Grown from Seed in Burkina Faso | InformativeBD

Introduction

Drinking water quality is one of the greatest factors affecting human health. However, the quality of the drinking water in many nations, particularly those that are developing, is not ideal, and this has led to an increase in the number of waterborne illnesses (Li and Wu, 2019).

Water pollution (surface and ground) may be considered as a naturally induced change in water quality or conditions induced directly by man’s numerous activities which render it unsuitable for food, human health, industry, agriculture, or leisure per suit (Dix, 1981). Toxic chemicals in water pose the greatest threat to the safety of drinking water and their effects are enormous and can cause damage to human health, crops, and aquatic organisms.

Physicochemical properties and heavy metal concentrations in the drinking water of San Francisco, Agusan Del Sur, Philippines

Synthetic chemicals such as herbicides and insecticides as well as fertilizer runoffs from agricultural farmlands and industrial discharge have the potential to impact negatively on human health since they block vital metabolic processes in the body. Runoffs from domestic houses, solid waste dumps, and commercial establishments may contain detergents and nutrients, which causes algae blooms in water bodies leading to eutrophication. Human waste excreta may contain a concentrated population of bacteria, pathogenic bacteria in untreated sewage, and may cause acute gastrointestinal illness. This phenomenon has rendered most surface water bodies polluted (Anim et al., 2010; Osei and Duker, 2008; Asante et al., 2008).

In the Philippines, water contamination of the surface water is due to exposure of chemicals which has been rampant, especially in areas exposed to industrial processes, such as but not limited to mining, agricultural processing, manufacturing, farming, and aquaculture according to Philippine Environment Monitor (Jalilov, 2017). Caraga, the mining capital of the Philippines, has more than 15 mining companies distributed in the region. Two of the mining companies are specifically located in Agusan del Sur which might have been affecting the Magdiwata Watershed which supplies water to the Municipality of San Francisco, Agusan del Sur (PSA, 2020).

The river network of Magdiwata Watershed extends from various municipalities of the province and is vulnerable to chemical contaminations. Periodic assessment of Magdiwata river networks has been conducted by the San Francisco Water District to ensure that the public water is free from waterborne microbes and chemical contaminants. However, external assessment, surveillance and/or monitoring must be done also to validate the test findings of the local supplier. Additional and external assessments for public drinking water support the integrity of water quality management.

As such, this research assessed the physicochemical properties and heavy metal contaminants in the public water system of San Francisco, Agusan del Sur before and after water treatment. Additionally, the assessment findings were evaluated against the existing and recent local and international drinking water standards which provided a picture of its general usability for drinking and utility purposes.

Reference

Anim F, Nyame FK, Armah TK. 2010. Coliform status of water bodies from two districts in Ghana, West Africa: implications for rural water resources management. Water Policy 1(12), 1–12. http://dx.doi.org/10.2166/wp.2010.013.

Asante KA, Quarcoopome T, Amevenku FYK. 2008. Water quality of the Weija Reservoir after 28 years of impoundment. West African Journal of Applied Ecology 13, 1–7.

Banana A, Gheethi A, Mohamed R, Efaq AN, Gawadi AMS. 2016. Quality of drinking water from wells and water treatment plants at West Libya. Conference paper.

Census of Population. 2015. Caraga. Total population by province, city, municipality, and barangay. PSA. Retrieved 20 June 2016.

Department of Health. 2017. Administrative Order No. 2017-0010 Re: Philippine National Standards for Drinking Water of 2017.

Department of Water, Government of Western Australia. Understanding salinity. Retrieved from wadow.clients.squiz.net.

Dix HM. 1981. Environmental pollution. John Wiley and Sons, Toronto, pp. 54–56.

Jalilov SM. 2017. Value of clean water resources: estimating the water quality improvement in Metro Manila, Philippines. Resources 7(1), 1. http://dx.doi.org/10.3390/resources7010001.

Kotoky P, Sarma B. 2017. Comparison of treatment efficiencies of the water treatment plants of Guwahati City of Assam, India. International Journal of Engineering and Technical Research 6(5), May 2017.

Lasheen MR, El-Kholy G, Sharaby CM, Elsherif IY, El-Wakeel ST. 2008. Assessment of selected heavy metals in some water treatment plants and household tap water in Greater Cairo, Egypt. Management of Environmental Quality: An International Journal 19(3), 367–376. https://doi.org/10.1108/14777830810866473.

Li P, Wu J. 2019. Drinking water quality and public health. Expo Health 11, 73–79. https://doi.org/10.1007/s12403-019-00299-8.

Osei FB, Duker AA. 2008. Spatial and demographic patterns of cholera in Ashanti region, Ghana. International Journal of Health Geographics 7, 44.

PhilAtlas. 2016. San Francisco, Province of Agusan del Sur. Retrieved from https://www.philatlas.com/mindanao/caraga/agusan-del-sur/san-francisco.html.

Philippine Statistics Authority (PSA). 2020. The Caraga asset account for mineral resources: 2015-2018. Retrieved from  https://rssocaraga.psa.gov.ph/sites/default/files/Caraga%20Asset%20Account%20for%20Mineral%20Resources%202015-2018.pdf.

San Francisco Water District (SFWD). 2020. San Francisco Water District’s technique and innovation.

Sastry S, Rao B, Nahata K. 2013. Study of parameters before and after treatment of municipal wastewater from an urban town. Global Journal of Applied Environmental Sciences 3(1), 41–48.

Water Quality Australia. 2013. Salinity and water quality. Retrieved from  https://www.waterquality.gov.au/issues/salinity.

World Health Organization. 1997. Guidelines for drinking water quality, 2nd edition, Volume 2. Health criteria and other supporting information. World Health Organization, Geneva, 9p.

World Health Organization. 2004. Guidelines for drinking water quality, 3rd edition, Volume 1.

World Health Organization. 2008. Guidelines for drinking water quality, 3rd edition – Incorporating the first and second addenda. Retrieved from www.who.int/publications/i/item/9789241547611.

World Health Organization. 2011. Guidelines for drinking water quality, 4th edition, Geneva.

World Health Organization. 2017. Guidelines for drinking water quality, 4th edition – Incorporating the first addendum. Retrieved from www.who.int/publications/i/item/9789241549950.

SourcePhysicochemical properties and heavy metal concentrations in the drinking water of SanFrancisco, Agusan Del Sur, Philippines 

 

Phenotypic Assessment of Six Cassava Families Grown from Seed in Burkina Faso | InformativeBD

Phenotypic evaluation of six cassava families (Manihot esculenta Crantz) from seed in Burkina Faso

Sawadogo O. Michel, Some Koussao, Ouedraogo M. Hamed, Tiama Djakaria, Tiendrebeogo Fidèle, Soro Monique, Tonde Wendmanegda Hermann, and Sawadogo Mahamadou, from the different institute of Burkina Faso. wrote a Reseach Article about, Phenotypic Assessment of Six Cassava Families Grown from Seed in Burkina Faso. Entitled, Phenotypic evaluation of six cassava families (Manihot esculenta Crantz) from seed in Burkina Faso. This research paper published by the International Journal of Biosciences (IJB). an open access scholarly research journal on Biosciences. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

Phenotypic markers are important in plant genetic characterisation studies. They are used in the present study to assess the phenotypic structuring of cassava genotypes obtained by biparental crossing. The plant material studied consists of 56 cassava genotypes from the third generation of vegetative reproduction following germination of seeds from six families resulting from crosses. To evaluate these genotypes, an Alpha lattice experimental design was used with three replicates and three blocks per replicate. Blocks I and II each contained 19 genotypes and block III 18 genotypes. Data was collected on 10 qualitative traits on leaves, stems and roots. All the variables evaluated presented several modalities. The frequencies showed that: the green-purple color (41%) was dominant for the apical leaf color characteristic. Stems color were predominantly light brown (30%). Green color (57%) was most common in the petioles. Genotypes showed more dichotomous ports (44%). In addition, the relative Shannon-Weaver diversity index (H’) was very high for all characters within genotypes (H’=0.90) and families (H’=0.66). The most polymorphic traits between genotypes were flowering ability (H’=1), stem color (H’=0.99), tuberous root texture (H’=0.97), apical leaf color (H’=0.96) and branching type (H’=0.93). The same index showed high intra-family diversity, family VI (H’= 0.83), family II (H’= 0.76), family IV (H’=0.69), family I (H’= 0.61), family III (H’= 0.53) and family V (H’= 0.52) showing high internal variability. ACH was used to structure the genetics into three phenotypic groups. This observed diversity can be used for cassava breeding in Burkina Faso.

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Read moreNatural Patch Power:Moringa Pods and Katakataka Leaves vs. Staphylococcus aureus | InformativeBD

Introduction

Manioc (Manihot esculenta Crantz 1766) is a perennial shrub 1 to 5 m high (Allem, 2002; Alves, 2002). It belongs to the class Dicotyledones, family Euphorbiaceae, genus Manihot and species Manihot esculenta Crantz (Isendahl, 2011; Soro, 2022). It has a diploid chromosome number of 2n=36 and a highly heterozygous genome (Alves, 2002). It is one of the most important tuberous root crops, highly valued for its starch content in tropical countries (N'Zué et al., 2014). Cassava is grown all over the world, particularly in West Africa (Agré et al., 2015). Cassava can be grown in areas with rainfall ranging from 500 mm to 8000 mm (François, 1989). Depending on the variety, production can be spread over a long period of the year, making the tuberous roots available when needed (François, 1989).

Phenotypic evaluation of six cassava families (Manihot esculenta Crantz) from seed in Burkina Faso

In recent years in Burkina Faso, climate variability has made farming very difficult. Crop diversification is very important to ensure food self-sufficiency. Tuber and root crops such as cassava can therefore be used to help achieve sustainable food security. In Burkina Faso, cassava production was estimated at around 17,081.25 tonnes in 2022 (FAOSTAT, 2024). As in all African countries, almost all cassava production in Burkina Faso is used for human and animal consumption (Amani et al., 2007). The tuberous roots are eaten raw or in the form of local dishes: boiled roots, grilled roots, placali, con'godê, attiéké and gari (Guira et al., 2017). In view of its food and nutritional potential, the quantities of cassava produced remain below national market demand, which in 2017 was estimated at around 124,917 tonnes of fresh tubers (Soro et al., 2022). In Burkina Faso, the major constraints to large-scale production are linked to several factors, namely: the long production cycle of six to 9 or even 12 months, the unsuitable quality of the soils used for its cultivation, which results in low root yields, the lack of suitable varieties, and the very narrow genetic base of cassava (Gmakouba et al., 2018). In order to meet consumer needs, production must be increased, and this requires efficient production technology based on the use of improved cassava varieties.

Phenotypic evaluation of six cassava families (Manihot esculenta Crantz) from seed in Burkina Faso

Exchanges of genetic material between producers mean that they end up with duplicates of the same cultivar (Soro et al., 2022). The reproduction of cassava, which is generally done by cuttings, leads to the spread of its bio-aggressors, which become more and more numerous and infest new fields. Studies carried out by Tiendrébéogo et al. (2009, 2012) reported the presence of Cassava Mosaic Diseases (CMD) in certain areas of Burkina Faso. Cassava is often grown under rainfed and irrigated systems in Burkina Faso. This is due to the earliness of the rains in relation to the length of the vegetative cycle and the poverty of the arable land, which means that average yields in farming areas are low, less than or equal to 15t/ha (FAOSTAT, 2024). In response to this situation, a great deal of research has been carried out by INERA through the introduction and evaluation of six (06) improved varieties, catalogued and popularised, TMS 4(2) 1425; TMS 91/02312; TMS 92/0067; TMS 92/0325; TMS 92/0427; TMS 94/0270) with potential yield (40/ha) (Gmakouba, 2018; Soro, 2022; MASA, 2014). But of these, only TMS 94/0270, commonly known as V5, is the most widely produced for its very good attiéké quality. To meet this challenge, new cassava varieties need to be developed, with a view to broadening the genetic base so as to obtain varieties that are tolerant to FGD, rich in beta-carotene, and with yields of up to 40 tonnes per hectare. It is therefore essential to assess the agro-morphological diversity of this cassava collection (Manihot esculenta Crantz) in order to better exploit the potential of these genotypes. This study was therefore carried out with the overall aim of determining the structure of the 56 genotypes obtained by biparental crossing. Specifically, the aim was (i) to determine the variability of genotypes through phenotypic traits and (ii) to identify the traits that best discriminate between genotypes and families.

Reference

Agré A, Dansi A, Rabbi I, Battachargee R, Dansi M, Melaku G. 2015. Agromorphological characterization of elite cassava (Manihot esculenta Crantz) cultivars collected in Benin. International Journal of Current Research in Biosciences and Plant Biology 2(2), 1–14. https://cgspace.cgiar.org/bitstream/handle/10568/58355/A.P.%20Agre,%20et%20al.pdf.

Alam MK. 2021. A comprehensive review of sweet potato (Ipomoea batatas [L.] Lam): Revisiting the associated health benefits. Trends in Food Science and Technology 115, 512–529. https://doi.org/10.1016/j.tifs.2021.07.001.

Allem AC. 2002. The origin and taxonomy of cassava. In: Hillocks RJ, Thresh JM, Bellotti AC, eds. Cassava: Biology, Production and Utilization. CABI Publishing, New York, 1–16. https://doi.org/10.1079/9780851995243.0001.

Alves AAC, Hillocks RJ, Thresh JM, Bellotti AC. 2002. Cassava botany and physiology. In: Cassava: Biology, Production and Utilization. CABI Publishing, London, 67–89. https://doi.org/10.1079/9780851995243.0067.

Bakayoko S, Soro D, N’dri B, Kouadio KK, Tschannen A, Nindjin C, Dao D, Girardin O. 2013. Étude de l’architecture végétale de 14 variétés améliorées de manioc (Manihot esculenta Crantz) dans le centre de la Côte d’Ivoire. Journal of Applied Biosciences 61, 4471–4477. https://doi.org/10.4314/jab.v61i0.85595.

Belhadj H, Medini M, Bouhaouel I, Amara H. 2015. Analyse de la diversité phénotypique de quelques accessions autochtones de blé dur (Triticum turgidum ssp. durum Desf.) du sud tunisien. 11.

Djirabaye N, Papa SS, Naïtormbaïdé M, Mbaïguinam JM, Guisse A. 2016. Agro-morphological characterization of cassava (Manihot esculenta Crantz) cultivars from Chad. Agricultural Sciences 7, 77049. https://doi.org/10.4236/as.2016.77049.

Elias M, McKey D, Panaud O, Anstett MC, Robert T. 2001. Gestion traditionnelle de la diversité morphologique et génétique du veuf par les Makushi Amérindiens (Guyana, Amérique du Sud): Perspectives pour la conservation à la ferme des ressources génétiques des cultures. Euphytica 120, 143–157. https://doi.org/10.1023/A:1017501017031.

FAOSTAT. 2024. Food and Agriculture Organization of the United Nations Statistics Division. https://www.fao.org/faostat/en/#home.

Fukuda WMG, Guevara CL, Kawuki R, Ferguson ME. 2010. Selected morphological and agronomic descriptors for the characterization of cassava. International Institute of Tropical Agriculture (IITA), Ibadan, Nigeria, 19.

Gashaw ET, Mekbib F, Ayana A. 2016. Genetic diversity among sugarcane genotypes based on qualitative traits. Advances in Agriculture 2016, Article ID 8909506, 8p. https://doi.org/10.1155/2016/8909506.

Gmakouba T, Some K, Traore ER, KpemouA KE, Zongo JD. 2018. Analyse de la diversité agromorphologique d’une collection de manioc (Manihot esculenta Crantz) du Burkina Faso. International Journal of Biological and Chemical Sciences 12(1), 402–421. http://www.ifgdg.org.

Guinko S. 1984. Végétation de la Haute Volta. Thèse de doctorat, Université Bordeaux III, 2 tomes, 556 p.

Guira F. 2016. Potentialités technologiques des racines de manioc à travers la production de l’attiéké: aspects nutritionnels, biochimiques, microbiologiques et moléculaires. Thèse de doctorat unique, Université Ouaga I Professeur Joseph KI-ZERBO, 173 p.

Isendahl C. 2011. The domestication and early spread of manioc (Manihot esculenta Crantz): A brief synthesis. Latin American Antiquity 22(4), 452–468.

Jain SK, Qualset CO, Bhatt GM, Wu KK. 1975. Geographical patterns of phenotypic diversity in a world collection of durum wheat. Crop Science 15, 700–704. https://doi.org/10.2135/cropsci1975.0011183X001500050026x.

Ka SL, Gueye M, Kanfany G, Diatta C, Mbaye MS, Noba K. 2020. Dynamique de levée des adventices du sorgho [Sorghum bicolor (L.) Moench] en zone soudanienne humide du Sénégal. International Review of Marine Science, Agronomy and Veterinary 8, 286–2930. http://www.ifgdg.org.

Mathura R, Dhander DG, Varma SP. 1989. Variability studies of cassava varieties on growth and yield under Tripura conditions. Journal of Root Crops 12, 25–28.

McKey D, Emperaireh L, Elias M, Pinton F, Robert T, Desmouliere S, Rival L. 2001. Gestions locales et dynamiques régionales de la diversité variétale du manioc en Amazonie, 26 p.

Médard R. 1973. Morphogénèse du manioc, Manihot esculenta Crantz, (Euphorbiacées-Crotonoidées): Étude descriptive. Adansonia 13, 483–494.

Ministère de l’Agriculture et de la Sécurité Alimentaire (MASA). 2014. Catalogue National des Espèces et Variétés Agricoles du Burkina Faso.

N’zué B, Okana M, Kouakou A, Dibi K, Zouhouri G, Essis B. 2014. Morphological characterization of cassava (Manihot esculenta Crantz) accessions collected in the centre-west, south-west, and west of Côte d’Ivoire. Greener Journal of Agricultural Sciences 4(6), 220–231. https://doi.org/10.15580/GJAS.2014.6.050614224.

Nartey F. 1978. Cassava cyanogenesis, ultrastructure, and seed germination. In: Denis R, Walter F, eds. Cassava. Copenhagen: Muksgaard, 234 p.

Raffaillac J-P, Second G. 2000. L’amélioration des plantes tropicales : le manioc.

Robooni T, Paul S, Rob M, Robert K. 2014. Combining ability analysis of storage root yield and related traits in cassava at the seedling evaluation stage of breeding. Journal of Crop Improvement 28(4), 530–546. http://www.tandfonline.com/loi/wcim20.

Sawadogo N, Naoura G, Ouoba A, Yaméogo N, Tiendrebeogo J, Ouedraogo MH. 2022. Phenotypical characteristics and genetic diversity of three types of sorghum [Sorghum bicolor (L.) Moench] cultivated in Burkina Faso based on qualitative traits. Moroccan Journal of Agricultural Sciences 3(2), 109–116. https://techagro.org/index.php/MJAS/article/view/941.

Sawadogo N. 2015. Diversité génétique des sorghos à grains sucrés [Sorghum bicolor (L.) Moench] du Burkina Faso. Thèse unique de doctorat, Université de Ouagadougou, 135 p.

Shannon CE, Weaver W. 1949. The mathematical theory of communication. University of Illinois Press, Urbana.

Soro M. 2022. Épidémiologie de la mosaïque du manioc (Manihot esculenta Crantz), diversité génétique et évaluation des accessions et variétés de manioc au Burkina Faso. Thèse unique de doctorat, Université Félix HOUPHOUËT BOIGNY, 184 p.

Tiendrébéogo F, Lefeuvre P, Hoareau M, Harimalala MA, De Bruyn A, Villemot J, Traoré VS, Konaté G, Traoré AS, Barro N, Reynaud B, Traoré O, Lett JM. 2012. Evolution of African cassava mosaic virus by recombination between bipartite and monopartite begomoviruses. Virology Journal 9(67).

Tiendrébéogo F, Lefeuvre P, Hoareau M, Traoré VSE, Barro N, Reynaud B, Traoré AS, Konaté G, Traoré O, Lett JM. 2009. Occurrence of East African cassava mosaic virus – Uganda (EACMV-UG) in Burkina Faso. Plant Pathology 58, 783.

SourcePhenotypic evaluation of six cassava families (Manihot esculenta Crantz) from seed in Burkina Faso   

Natural Patch Power: Moringa Pods and Katakataka Leaves vs. Staphylococcus aureus | InformativeBD

Moringa pods (Moringa oleifera) and katakataka leaves (Kalanchoe pinnata) extract as a natural-derived medical patch against Staphylococcus aureus

Cristine Joyce S. Buenaventura, Catherine B. Balaguer, Alexandrine Erica D. Barcelon, Ayessa Mae D. Cortes, Denise Mikaela A. Doroja, and Darylle Cesar G. Hilapo, from the different institute of Philippines. wrote a Reseach Article about, Natural Patch Power: Moringa Pods and Katakataka Leaves vs. Staphylococcus aureus. Entitled, Moringa pods (Moringa oleifera) and katakataka leaves (Kalanchoe pinnata) extract as a natural-derived medical patch against Staphylococcus aureus. This research paper published by the International journal of Microbiology and Mycology (IJMM). an open access scholarly research journal on Microbiology . under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

This study investigated the effects of Moringa pods (Moringa oleifera) and Katakataka leaves (Kalanchoe pinnata) extracts on Staphylococcus aureus (S. aureus), a bacterium often causing skin infections. The researchers prepared ten treatments using a 95% ethyl alcohol solution and dried plants, which were then tested for their inhibitory effects on S. aureus growth. The results showed that treatments with Moringa pods extract, both alone and combined with a medical patch, significantly inhibited S. aureus growth, with zones of inhibition measuring 2.4cm and 2.7cm respectively. Conversely, Katakataka leaves extract showed little to no inhibition and even seemed to facilitate S. aureus growth. Statistical analysis using One-way ANOVA and Tukey’s HSD test revealed significant differences between treatments, with those containing a higher percentage of Moringa pods extract proving more effective. This suggests that Moringa pods extract could be a potent natural-derived medical patch against S. aureus.

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Read moreControlling Fruit Fly in Bitter Gourd Using Sesame Leaf Extract | InformativeBD

Introduction

In order to keep the skin's physiological functions working, wound healing is a necessary procedure. Thus, if bacteria enter a wound and begin to multiply, an infection may develop, impeding the healing process of the wound (Leonard, 2023). The best technique for wound healing and infection control is dressing application. This lessens discomfort and improves the hypoxic environment's ability to promote healing (Nguyen et al., 2023). It also helps to maintain the environment's moisture content and temperature. Herbs have been utilized by humans for wound care since the dawn of time. According to a 2019 study by Doña et al., alternative medicine is becoming more popular due to the high cost of synthetic drugs and the possibility of genetic resistance developing in some microorganisms. Because of its uses in conventional medicine, the medicinal plant Kalanchoe pinnata is known to demonstrate antibacterial efficacy against a variety of diseases and their mechanisms of action, according to Tajudin et al. (2022).

The amazing tree of Moringa oleifera is rich in bioactive substances and a good source of pharmaceutical compounds including flavonoids, phenolic acid, and polyphenols, it is thought to have medical benefits like antioxidant, tissue protection, antiinflammatory, and analgesic (Chis et al., 2024). Natural polymers represent a potential class of materials for the development of skin wound dressings that can hasten the healing process and boost defense against infections (Ansari and Darvishi, 2024). Moreover, skin has extraordinary regenerating capabilities. When this regeneration process is occasionally disrupted and wounds heal slowly, patients face serious health risks because the available patches, dressings, and gauzes are insufficient to initiate a physiological wound healing process, which can lead to the formation of new lesions.

The purpose of this study is to investigate the possible application of Katakataka leaves (Kalanchoe pinnata) and Moringa pods (Moringa oleifera) extract as a naturally derived antibacterial medical patch.

Reference

Afolayan AJ, Bradley G, Sagbo IJ. 2017. Antioxidant, antibacterial and phytochemical properties of two medicinal plants against the wound infecting bacteria. Asian Pacific Journal of Tropical Biomedicine 7(9), 817–825.

Agustin Y, Antonius YJ, Gondokesumo M. 2023. Effectivity of patch herbal mixture composed of mangosteen peel extract and bacterial cellulose for wound healing. Pharmacognosy Journal 15(3), 461–466.

Alexey G, Ilona G, Irina S, Ivan S, Oleg P, Vladimir K. 2018. Biological activities of derived bioactive components from Moringa species: An overview. Entomology and Applied Science Letters 5(1), 82–87.

Almatrafi M, Fernandez ML, Vergara-Jiménez M. 2017. Bioactive components in Moringa oleifera leaves protect against chronic disease. Antioxidants 6(4), 91. https://doi.org/10.3390/antiox6040091

Annisa R, Ervianingsih N, Kamaruddin I, Langkong J, Mursyid M, Zahran I. 2019. Antimicrobial activity of moringa leaf (Moringa oleifera) extract against the growth of Staphylococcus epidermidis. IOP Conference Series Earth and Environmental Science 343(1), 012145. https://doi.org/10.1088/1755-1315/343/1/012145

Arvind Bharani RS, Jini Angel K, Rajsekhar PB, Rajsekhar SPV, Ramachandran M. 2016. The “wonder plant” Kalanchoe pinnata (Linn.) Pers.: A review. Journal of Applied Pharmaceutical Science 6(03), 151–158.

Athanassiou A, Bertorelli R, Fiorentini F, Grisoli P, Suarato G, Zych A. 2021. Plant-based biocomposite films as potential antibacterial patches for skin wound healing. European Polymer Journal 150, 110414. https://doi.org/10.1016/j.eurpolymj.2021.110414

Bagon A, Evales E, Granada M, Intong J, Marcos C, Munez K, Nonan C, Panare K, Parapan C, Potencioso A, Tan C. 2006. The antimicrobial activity of 100% katakataka leaf extract (Kalanchoe pinnata) against Staphylococcus aureus. Department of Science and Technology–Philippine Council for Health Research and Development Information Network. https://www.herdin.ph/index.php?view=research&cid=52752

Bhowmik D, Khosla KK, Matthew C, Matthew S. 2013. Preliminary phytochemical studies of Kalanchoe pinnata (Lam.) Pers. ResearchGate. https://www.researchgate.net/publication/304148551_Preliminary_phytochemical_studies_of_Kalanchoe_pinnata_Lam_Pers

Britto E, Nezwek T, Popowicz P, Robins M. 2023. Wound dressings. StatPearls – National Center for Biotechnology Information. https://www.ncbi.nlm.nih.gov/books/NBK470199/

Chinn R, Sehulster L. 2024. Regulated medical waste. Centers for Disease Control and Prevention 14. https://www.cdc.gov/infection-control/hcp/environmental-control/regulated-medical-waste.html

Chiș A, Cozma A, Fodor A, Hegheș S, Kamgang R, Mureșan C, Noubissi P, Orășan O, Pop O, Sitar-Tăut A, Suharoschi R, Tagne M, Vulturar R. 2023. Bioactive compounds in Moringa oleifera: Mechanisms of action, focus on their anti-inflammatory properties. Plants 13(1), 20. https://doi.org/10.3390/plants13010020

Coutinho P, Correia I, Miguel SP, Ribeiro MP, Simões D. 2018. Recent advances on antimicrobial wound dressing: A review. European Journal of Pharmaceutics and Biopharmaceutics 127, 130–141. https://doi.org/10.1016/j.ejpb.2018.02.022

Cui X, Huang W, Li J, Liu X, Shi S, Tian W, Tu P, Wang Y. 2022. Biosynthesis investigations of terpenoid, alkaloid, and flavonoid antimicrobial agents derived from medicinal plants. Antibiotics (Basel). National Library of Medicine, National Center for Biotechnology Information.

Dahikar SB, Patil DN, Pattewar SV. 2013. Antimicrobial potential of extract from leaves of Kalanchoe pinnata. International Journal of Pharmaceutical Sciences and Research 4(12), 4577–4580. https://doi.org/10.13040/IJPSR.0975-8232.4(12).4577-80

Delekta P, Hammer N, Lydic T, Mulks M, Shook J. 2018. Staphylococcus aureus utilizes host-derived lipoprotein particles as sources of fatty acids. Journal of Bacteriology 200(14). https://doi.org/10.1128/JB.00728-17

Dino KP, Doña JJ, Loyola NE. 2019. Effectiveness of Katakataka leaves extract as an antibacterial against S. epidermidis and E. coli. Ascendens Asia Journal of Multidisciplinary Research Abstracts 3(2). https://ojs.aaresearchindex.com/index.php/AAJMRA/article/view/4075

DiPietro L, Guo S. 2010. Factors affecting wound healing. Journal of Dental Research 89(3), 219–229.

Dixit S, Kumar P, Tripathi A. 2016. Medicinal properties of Moringa oleifera: A review. ResearchGate. https://www.researchgate.net/publication/304897997_MEDICINAL_PROPERTIES_OF_Moringa_oleifera_A_REVIEW

Dmitriev B, Ehlers S, Holst O, Rietschel E, Toukach F. 2004. Tertiary structure of Staphylococcus aureus cell wall murein. Journal of Bacteriology 186(21), 7140–7144. https://pubmed.ncbi.nlm.nih.gov/15489425/

Dong R, Guo B. 2021. Smart wound dressings for wound healing. Nano Today 41, 101290. https://doi.org/10.1016/j.nantod.2021.101290

Edwards R, Harding K. 2004. Skin and soft tissue infections: Bacteria and wound healing. Current Opinion in Infectious Diseases 17(2), 91–96.

Farahani M, Shafiee A. 2021. Wound healing: From passive to smart dressings. Advanced Healthcare Materials 10(16). https://doi.org/10.1002/adhm.202100477

Ferreira MGR, Guimarães MCM, Lima RA, Oliveira CLLG, Santos MRAI. 2014. Callogenesis in leaves of Kalanchoe pinnata Lam. by 2,4-D and BA action. Revista Brasileira de Plantas Medicinais 16(3 suppl 1), 760–764.

Gao B, Li M, Li X, Lu L, Yan Y, Zhang C. 2021. Research progress on antibacterial activities and mechanisms of natural alkaloids: A review. Antibiotics (Basel) 10(3), 318. https://doi.org/10.3390/antibiotics10030318

Ghomi E, Khalili S, Khorasani SN, Neisiany RE, Ramakrishna S. 2019. Wound dressings: Current advances and future directions. Journal of Applied Polymer Science 136(27), 47738. https://doi.org/10.1002/app.47738

Godinho EB, Müller I, Rossi-Bergmann B. 1993. In vitro spleen cell proliferation following in vivo treatment with a synthetic glycolipid or lipid A in three mouse strains. Immunopharmacology 25(2), 143–153.

Hakala T, Hakkarainen T, Karhukorpi J, Turtiainen J. 2014. The impact of surgical wound bacterial colonization on the incidence of surgical site infection after lower limb vascular surgery: A prospective observational study. European Journal of Vascular and Endovascular Surgery 47(4), 411–417. https://doi.org/10.1016/j.ejvs.2013.12.025

Hasan MR, Hossen F, Islam Z, Islam SMR, Karim R, Mahtab-ul-Islam K. 2021. Moringa oleifera is a prominent source of nutrients with potential health benefits. International Journal of Food Science 2021, 1–11.

Hewawasam RP, Janesha UGS, Rathnayake H, Wijayaratne WMDGB. 2020. In vitro evaluation of the antimicrobial activity of leaf extracts of Litsea iteodaphne against a selected group of bacteria including methicillin-resistant Staphylococcus aureus. Advanced Biomedical Research 9, 21.

Horswill AR, Keim KC. 2023. Staphylococcus aureus. Trends in Microbiology 31(12), 1300–1301. https://doi.org/10.1016/j.tim.2023.07.001

Ismail INA, Tajudin NJ. 2022. Antimicrobial activity of Kalanchoe pinnata: A review. Malayan Journal of Science, Health & Technology. https://oarep.usim.edu.my/jspui/bitstream/123456789/18752/1/Antimicrobial%20Activity%20of%20Kalanchoe%20Pinnata%20A%20Review.pdf

Kloos WE, Schleifer KH. 1986. Genus Staphylococcus. In: Bergey’s Manual of Systematic Bacteriology, Vol. 2, 1013–1035. Williams & Wilkins, Baltimore.

Le HNT, Le TTN, Nguyen AT, Nguyen HM, Pham TT. 2023. Biomedical materials for wound dressing: Recent advances and applications. RSC Advances 13(8), 5509–5528.

Leonard J. 2023. How to recognize and treat an infected wound. https://www.medicalnewstoday.com/articles/325040#summary

Libretexts. 2021. Safety procedures for the microbiology laboratory. Biology LibreTexts. https://bio.libretexts.org/Courses/North_Carolina_State_University/MB352_General_Microbiology_Laboratory_2021_(Lee)/01%3A_Laboratory_Safety/1.01%3A_Safety_Procedures_for_the_Microbiology_Laboratory

Malhotra SPK, Mandal TK. 2018. Phytochemical screening and in vitro antibacterial activity of Moringa oleifera Lam. leaf extract. Archives of Agriculture and Environmental Science 3(4), 367–372.

Monton C, Panrat K, Pichayakorn W, Sampaopan Y, Suksaeree J. 2022. Herbal transdermal patches made from optimized polyvinyl alcohol blended film: Herbal extraction process, film properties, and in vitro study. Journal of Drug Delivery Science and Technology 69, 103170.

National Institute of Open Schooling in India. n.d. Microbiology, pg. 34 (Lesson 3: Nutrition and Growth of Bacteria). https://nios.ac.in/media/documents/dmlt/Microbiology/Lesson-03.pdf

Nnamdi U, Okwu E. 2011. Two novel flavonoids from Bryophyllum pinnatum and their antimicrobial activity. Journal of Chemical and Pharmaceutical Research 3(2), 1–10.

Nwadinigwe A. 2011. Antimicrobial activities of methanol and aqueous extracts of the stem of Bryophyllum pinnatum Kurz (Crassulaceae). African Journal of Biotechnology 10(72). https://doi.org/10.5897/ajb11.1000

Stefanović OD. 2018. Synergistic activity of antibiotics and bioactive plant extracts: A study against Gram-positive and Gram-negative bacteria. InTech eBooks. https://doi.org/10.5772/intechopen.72026

Wilkinson BJ. 1997. The staphylococci in human disease. In: The Biology of Staphylococci, 1–38. Churchill Livingstone, New York, NY, USA.

Yan Y, Li X, Zhang C, Lv L, Gao B, Li M. 2021. Research progress on antibacterial activities and mechanisms of natural alkaloids: A review. Antibiotics (Basel) 10(3), 318. https://doi.org/10.3390/antibiotics10030318

SourceMoringa pods (Moringaoleifera) and katakataka leaves (Kalanchoe pinnata) extract as anatural-derived medical patch against Staphylococcus aureus  

Controlling Fruit Fly in Bitter Gourd Using Sesame Leaf Extract | InformativeBD

Control of fruit fly (Batrocera cucurbitae S.) with sesame leaf ethanolic extract in bitter gourd (Momordica charantia L.)

Jonathan S. Balog, Lucila V. Rocha, Artemio A. Martin Jr., Raphy A. Sugue, and Archival B. Sabado, from the different institute of Philippines. wrote a Reseach Article about, Controlling Fruit Fly in Bitter Gourd Using Sesame Leaf Extract. Entitled, Control of fruit fly (Batrocera cucurbitae S.) with sesame leaf ethanolic extract in bitter gourd (Momordica charantia L.).This research paper published by the International Journal of Agronomy and Agricultural Research (IJAAR)an open access scholarly research journal on Agronomy . under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

The increasing demand for eco-friendly agricultural practices has spurred interest in the development of botanical pesticides. The study aimed to investigate the effects of sesame leaf extract (ethanolic) to control insect pests of bitter gourd, Momordica charantia L. specifically fruit fly, Batrocera cucurbitae S. and to check its effect on the agronomics of the test crop. The study was conducted at Isabela State University – Cabagan campus for dry season C.Y. 2023 only. The treatments involved one negative control, one positive control (using commercial synthetic insecticide), pure sesame leaf extract and four treatments with varying concentration of sesame leaf ethanolic extract. Growth parameters (plant length), pest infestation rates, and yield components (number of fruits and average fruit weight) were measured. Results of the statistical analysis using Statistical Tool for Agricultural Research (STAR) software under Two-Factorial Randomized Complete Block Design revealed certain results. Hybrid variety consistently outclassed open pollinated variety on all agronomic parameters. The application of commercially available synthetic insecticide (T2) had recorded highest numbers in almost all parameters while plots applied with pure sesame leaf extract (T3) and sesame leaf ethanolic extract (T4-T7) also logged higher numbers compared to the untreated plants (T1) suggesting that the treatments employed had positive results. Economically, the use of 105ml/l sesame leaf ethanolic extract can be used hand-in-hand with commercial pesticide for better pest control especially fruit fly in bitter gourd. These results support the integration of botanical pesticides into sustainable agriculture and provide foundation for further explorations into naturally derived crop protection strategies.

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Read moreInsect Diversity in Okra Cultivation in Man, Côte d’Ivoire | InformativeBD 

Introduction

The vegetable Momordica charantia L., Cucurbitaceae, is known variously as bitter gourd, balsam pear, bitter melon, bitter cucumber, and African cucumber Bitter gourd (Behera et al., 2010) The genus Momordica is a native of the Paleotropics and comprises about 60 species. Bitter gourd grows in tropical and subtropical areas, including parts of East Africa, Asia, the Caribbean, and South America, where it is used not only as a food but also as a medicine. The plant is monoecious, annual climber with long-stalked leaves and yellow, solitary male and female flowers borne on the leaf axils. The warty and oblong or elliptical-shaped fruit is botanically a ‘pepo.’ The plant grows well in a variety of soils and begins flowering about one month after planting (Asna et al., 2020). It has been part of the Filipino diet since time immemorial. All succulent parts of the plant have been consumed as viand by Filipino households to wit it has been shown to have essential nutrients that is beneficial to humans. Due to the medicinal properties of the plant, some companies have also made herbal supplements out of this crop. 

In Isabela, the major producers of bitter gourd are the municipalities of Roxas, Aurora, Mallig, Reina Mercedes, and the Cauayan city according to the Department of Agriculture. 

Control of fruit fly (Batrocera cucurbitae S.) with sesame leaf ethanolic extract in bitter gourd (Momordica charantia L.)

Though according to the report of Philippine Statistics Authority, the regionwide production data states that the production volume of bitter gourd declines by 14% in 2020.

Bitter gourd (Momordica charantia L.) is a commercially and nutritionally important market vegetable in Asia cultivated mainly by smallholder farmers (Dhillon et al., 2018). 

Households generally purchase vegetables three times a week and predominantly from the wet market. While most households consider price as their primary criteria for purchase, quality in use is considered important. Wives continue to play a major role in the decision to purchase, cook and serve vegetables. Stakeholders in the vegetable supply chain, including smallholder farmers can focus their strategies to develop a strong domestic market for vegetables through increased consumption, and better-quality management systems to defend their products against the threat of imports (Concepcion, 2005).

Insect pests are a major constraint for increasing the production and productivity of this Bitter gourd (Momordica charantia L.). Bitter gourds are attacked by several insect pests, among them the fruit fly is one of the most destructive insect-pests (Panday et al., 2008). Melon fruit flies (Diptera: Tephritidae: Dacinae) are economically important pests of the cucurbits and are geographically distributed throughout the tropics and subtropics of the world (Chinajariyawong et al., 2003), especially in most countries of South East Asia (Allwood et al., 1999). The extent of losses varies between 30 and 100% depending on the cucurbit species and the season (Pareek and Kavadia, 1995; Kapoor, 1993; Panday et al., 2009). The melon fly has been observed on 81 host plants, with watermelon being a highly-preferred host, and has been a major limiting factor in obtaining good-quality fruits and high yield (Nath and Bhushan, 2006). 

The term pesticide covers a wide range of compounds including insecticides, fungicides, herbicides, rodenticides, molluscicides, nematicides, plant growth regulators and others.

Ideally a pesticide must be lethal to the targeted pests, but not to non-target species, including man. Unfortunately, this is not the case, so the controversy of use and abuse of pesticides has surfaced. That is aside from the fact that the cause of pesticide is also an addition to the costs of production.

As a result of the recent efforts, made by the Environmental Protection Agency, to reduce the use of harmful insecticides, especially, organophosphates, organochlorines, some carbamates and pyrethroids, in the agricultural crops, the trend has now shifted towards an integrated pest management (IPM) for the control of tephritid fruit flies (Roger et al., 2010).

A study had found that the phytochemical result of leaf and stem ethanolic extract indicated the presence of certain phytochemicals such as alkaloids, carbohydrates, cardiac glycosides, diterpenoids, flavonoids, proteins, saponins, steroids, tannins and triterpenoids that were proved to be vital in the insecticidal activity of the extracts. Thus, the stem and leaf ethanolic extracts of sesame are effective botanical insecticides against C. tomentosicollis especially at 20.00 mg/l of the leaf extract. With this result, it may also be effective to fruit fly with the same geniality and may help reduce the use of pesticides for the sustainable agriculture.

Generally, the study aims to evaluate the effectiveness of sesame leaf ethanolic extract to control fruit fly (Batrocera cucurbitae S.) on bitter gourd fruits.

Specifically, it aims to evaluate the efficacy of sesame leaf ethanolic extract on fruit fly (Batrocera cucurbitae S.), assess effect of sesame leaf ethanolic extract on fruit fly (Batrocera cucurbitae S.) on the growth and yield of bitter gourd, determine the most effective level and best method of application of sesame plant ethanolic extract responsive to Batrocera cucurbitae S. in bitter gourd and analyze the cost and return of the different treatments.

Reference

Ampalaya Production Guide. n.d. Pinoy Bisnes. https://www.pinoybisnes.com/agri-business/ampalaya-production-guide/

Ampalaya. n.d. Department of Agriculture – Cagayan Valley. https://cagayanvalley.da.gov.ph/wp-content/uploads/2018/02/Ampalaya.pdf

Asna AC, Joseph J, Joseph John K. 2020. Botanical description of bitter gourd. The bitter gourd genome, 7–31. https://link.springer.com/chapter/10.1007/978-3-030-15062-4_2

Behera TK, Behera S, Bharathi LK, John KJ, Simon PW, Staub JE. 2010. Bitter gourd: Botany, horticulture, breeding. Horticultural Reviews 37, 101–141.

Clarke AR. 1986. Fruit flies (Tephritidae): Their exploitation in agricultural systems. In: van der Werf E, De Meyer PA (eds.), Integrated fruit fly management, 1–16. Academic Press.

Concepcion SB. 2005. Consumer market segments in the Philippine vegetable industry.

Dhillon NP, Sanguansil S, Srimat S, Schafleitner R, Manjunath B, Agarwal P, McCreight JD. 2018. Cucurbit powdery mildew-resistant bitter gourd breeding lines reveal four races of Podosphaera xanthii in Asia. HortScience 53(3), 337–341.

Duvick DN. 2005. The contributions of breeding to yield advances in maize. In: Advances in Agronomy 86, 83–145. Academic Press.

Hernandez R, Ramirez A. 2010. Influence of pesticide management on the yield parameters of squash (Cucurbita pepo) crops. Journal of Agricultural and Food Chemistry 58(12), 7353–7360.

Isman AA. 2006. Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world. Annual Review of Entomology 51, 45–66.

Mishra SK, Singh P. 2012. Economic viability of botanical pesticides in integrated pest management of vegetable crops. Journal of Sustainable Agriculture 30(3), 210–219.

Mulei EW, Gichuru P. 2018. A cost-benefit analysis of botanical insecticides versus synthetic pesticides for insect pest management in maize. Journal of Agricultural Economics and Development 4(1), 45–53.

Pavela R, Benelli G. 2016. Essential oils as ecofriendly biopesticides. Chemistry Central Journal 10(1), 1–13.

Philippine Council for Agriculture, Forestry, and Natural Resources Research and Development. 2009. Enhanced yield potential and postharvest quality of bitter gourd [Final report].

Prevent losses by bagging your ampalaya fruits. 2005. PhilStar Agriculture. https://www.philstar.com/business/agriculture/2005/11/06/305486/prevent-losses-bagging-your-ampalaya-fruits

Reddy PM, Agrawal SK, Prasad D. 2011. Evaluation of insecticide treatments for the management of pest infestation in bitter gourd. Indian Journal of Agricultural Research 45(1), 45–50.

Regnault-Roger C, Vincent C, Arnason JT. 2012. Essential oils in insect control: Challenges and opportunities. Trends in Parasitology 28(7), 326–331.

Sahu PK, Sinha J. 2005. Morpho-biometrical analysis of bitter gourd (Momordica charantia L.) cultivars. Journal of Plant Breeding and Crop Science 1(2), 67–72.

Singh B, Sharma S, Gupta R. 2008. Damage assessment and symptomatology of fruit fly infestation in cucurbit crops. Indian Journal of Entomology 70(2), 150–156.

Singh N, Singh BP, Singh SK. 2002. Phenotypic variability in bitter gourd (Momordica charantia L.) for fruit yield and quality. Indian Journal of Agriculture Science 72(1), 78–81.

University of the Philippines Los Baños, Institute of Plant Breeding. n.d. Integrated pest management in cucurbits [Extension Bulletin].

Walia R, Kaur A, Singh R. 2013. Occurrence and symptom development of fruit fly infestation in bitter gourd. Journal of Pest Science 86(2), 145–152.

Source : Control of fruit fly (Batrocera cucurbitae S.) with sesame leaf ethanolic extract in bitter gourd (Momordica charantia L.)

 

 

 

Insect Diversity in Okra Cultivation in Man, Côte d’Ivoire | InformativeBD

Diversity and abundance of insects found on okra Abelmonchus esculentus cultivation in Man, Côte d’Ivoire

Diabate Dohouonan, Coulibaly Tenon, N’guessan Ehikpa Naomie Melin , and Tano Yao, from the different institute of Côte d’Ivoire. wrote a Reseach Article about, Insect Diversity in Okra Cultivation in Man, Côte d’Ivoire. Entitled, Diversity and abundance of insects found on okra Abelmonchus esculentus cultivation in Man, Côte d’Ivoire. This research paper published by the International Journal of Biosciences (IJB). an open access scholarly research journal on Biosciences. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

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 21th to 70th Day After Sowing, on Clemson spineless okra sown on March 2nd, 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.

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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.

Reference

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.

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.

Source Diversity and abundance of insects found on okra Abelmonchus esculentus cultivation in Man, Côted’Ivoire