Physicochemical Parameters of Amazah Rock Pool Habitats of Mosquito Larvae and Species Diversity of Indoor-Resting Mosquito of Nearby Lamingo Communities, Jos-North LGA of Plateau State, Nigeria


Authors : Daben, M. R.; Taiwo, M. E.; Njila, L. H.; Beshel, S. B.; Lumi, E. B.; Mwansat, G. S.

Volume/Issue : Volume 11 - 2026, Issue 2 - February


Google Scholar : https://tinyurl.com/2s4m52fs

Scribd : https://tinyurl.com/yfcuy2s3

DOI : https://doi.org/10.38124/ijisrt/26feb658

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Abstract : Mosquitoes are cosmopolitan and are mostly found in freshwater bodies such as ponds, drainages, sewages, stagnant and slow flowing rivers. The study investigated physicochemical parameters of rock-pool mosquito larval habitats of Amazah and species diversity of indoor-resting mosquitoes in Lamingo villages. Three sampling points (A, B and C) were randomly selected; and physicochemical parameters that include pH, temperature, dissolved oxygen (DO), total dissolved solids (TDS), conductivity, turbidity, salinity and depth were conducted. Adult mosquitoes were sampled from 30 households of nearby communities of the rock pool larval habitats, by pyrethrum spray. Mosquitoes collected, were identified using standard keys. The physicochemical properties results revealed significance difference (p ≤ 0.05) between Depth and TDS. Total of 252 larvae collected, belongs to Anopheline and Culicine group. Anopheles spp., were the most abundant 180, closely followed by Culex spp. (72) (t = 45.089, df = 2, p < 0.001). Anopheles larval mosquitoes spp., were commonly found in shallow pools with higher TDS levels; while Culex spp., were found in deeper pools. Anopheline species appear to prefer polluted and unclean water ponds. A total of 208 (f-ratio 14.8159. p = 0.0006) indoor-resting adult mosquitoes of nearby communities collected, belongs to 3 genera. Culex was the most dominant [RA = 47.11%; closely followed by Anopheles, RA = 44.23% and the least was Aedes, RA = 8.65%, diversity index (H) = 5.49]. The study concluded with greater health implications and the need for targeted vector control; which may involve proper environmental management strategies that can curtail prevalence of mosquito-borne diseases within the localities.

Keywords : Abundance, Diversity, Indoor-Resting, Mosquitoes, Physicochemical.

References :

  1. Adebote, D. A., Oniye, S. I., and Muhammed, Y. A. (2008). Studies on mosquitoes breeding in rock pools on inselbergs around Zaria, northern Nigeria. Journal of Vector Borne Diseases, 45: 21–28.
  2. Adebote, D. A., Oniye, S. I., and Muhammed, Y. A. (2008). Studies on mosquitoes breeding in rock pools on inselbergs around Zaria, northern Nigeria. Journal of Vector Borne Diseases, 45: 21–28.
  3. Afolab, B. B., Okoromah, C. A. N. (2004). Intramuscular arteether for treating severe malaria. Cochrane Database of Systematic Reviews. 2004 (4). DOI: 10.1002/14651858.CD004391.pub2.
  4. Afolabi, O. J., Akinneye, J. O., and Igiekhume, A. M. A. (2019). Identification, abundance, and diversity of mosquitoes in Akure South Local Government Area, Ondo State, Nigeria. The Journal of Basic and Applied Zoology, 80: 37. https://doi.org/10.1186/s41936-019-0112-4.
  5. Afrane, Y. A., Lawson, B. W., Brenya, R., Kruppa, T., and Yan, G. (2012). The ecology of mosquitoes in an irrigated vegetable farm in Kumasi, Ghana: abundance, productivity and survivorship. Parasites & Vectors, 5: 233. http://www.parasitesandvectors.com/content/5/1/233.
  6. Akeju, A. V., Olusi, T. A., and Simon‑Oke, I. A. (2022). Effect of physicochemical parameters on Anopheles mosquitoes larval composition in Akure North Local Government area of Ondo State, Nigeria. The Journal of Basic Zoology, 83: 34. https://doi.org/10.1186/s41936-022-00298-3.
  7. Akeju, A. V., Olusi, T. A., and Simon‑Oke, I. A. (2022). Effect of physicochemical parameters on Anopheles mosquitoes larval composition in Akure North Local Government area of Ondo State, Nigeria. The Journal of Basic Zoology, 83: 34. https://doi.org/10.1186/s41936-022-00298-3.
  8. Alyasiri, A. J., and Jassum, A. S. (2025). Mosquito-borne diseases: a review of the risks to humans, Iraq. Current Research in Interdisciplinary Studies, 4(2): 1–15.
  9. Attaullah, M., Gula, S., Bibia, D., Andaleeba, A., Ilahia, I., Sirajb, M., Ahmada, M., Ullaha, I., Alia, M., Ahmada, S., and Ullah, Z. (2023). Diversity, distribution and relative abundance of the mosquito fauna (Diptera: Culicidae) of Malakand and Dir Lower, Pakistan. Brazilian Journal of Biology, 83: e247374. https://doi.org/10.1590/1519-6984.247374.
  10. Avramov, M., Thaivalappil, A., Ludwig, A., Miner, L., Cullingham, C. I., Waddell, L., and Lapen, D. R. (2024). Relationships between water quality and mosquit presence and abundance: a systematic review and meta-analysis. Journal of Medical Entomology, 61(1): 1–33. https://doi.org/10.1093/jme/tjad139.
  11. Bayoh, M. N., and Lindsay, S.W. (2003). Effect of temperature on the development of the aquatic stages of Anopheles gambiae sensu stricto (Diptera: Culicidae). Bulletin of Entomological Research, 93, 375–381.
  12. Boerlijst, S.P., Johnstonc, E.S., Ummels, A.,  Krol, L., Boelee, E., van Bodegoma, P.M., and Schrama, M.J.J. (2023). Biting the hand that feeds: Anthropogenic drivers interactively make mosquitoes thrive. Science of the total Environment, 858: 159716. http://dx.doi.org/10.1016/j.scitotenv.2022.159716.
  13. Cable, J., Barber, I., Boag, B., Ellison, A. R., Morgan, E. R., Murray, K., Pascoe, E. L., Sait, S. M., Wilson, A. J., and Booth, M. (2017). Global change, parasite transmission and disease control: lesson from ecology. Philosophical Transaction R. Soc. B. 372: 20160088. https://dx.doi.org/10.1098/rstb.2016.0088.
  14. Chaves, L. S. M., BergoI, E.S., Jan E. Conn, J. E., Laporta, G. Z., Prist, P. R., and Sallum, M. A. M. (2021). Anthropogenic landscape decreases mosquito biodiversity and drives malaria vector proliferation in the Amazon rainforest. PLoS ONE Negl. Trop. Dis., 16(1): e0245087. https://doi.org/10.1371/journal.pone.0245087.
  15. Chibuike, I. F. (2022). Preliminary Study on the Ecology and Diversity of Mosquito Species in Nnamdi Azikiwe University Hostels, Awka, Anambra State. Acta Scientific Veterinary Sciences 4(7): 11-16.
  16. Doeurk, B., Leng, S., Long, Z., Maquart, P-O., and Boyer, S. (2025). Impact of temperature on survival, development and longevity of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Phnom Penh, Cambodia. Parasites & Vectors, 18:362. https://doi.org/10.1186/s13071-025-06892-y
  17. Emidi, B., Kisinza, W. N., Mmbando, B. P., Malima, R. and Mosha, F. W. (2017). Effect of physicochemical parameters on Anopheles and Culex mosquito larvae abundance in different breeding sites in a rural setting of Muheza, Tanzania. Parasites & Vectors, 10:304. DOI 10.1186/s13071-017-2238-x.
  18. Fan, Z., Zhao, T., Gu, Z., Gao, H., Zhou, X., Yu, H., Xing, D., Wang, H., and Li, C. (2025). Differences in human skin volatiles between populations with high and low attraction to mosquitoes. Parasites & Vectors, 18:183. https://doi.org/10.1186/s13071-025-06738-7.
  19. Giraldo, D., Rankin-Turner, S., Corver, A., Tauxe, G. M., Gao, A.L., Jackson, D. M., Simubali, L., Book, C., Stevenson, J. C., Thuma, P. E., McCoy, R. C., Gordus, A., Mburu, M. M., Simulundu, E., McMeniman, C. J. (2023). Human scent guides mosquito thermotaxis and host selection under naturalistic conditions. Curr Biol., 33(12): 2367-2382.
  20. Gyawali, N., Russell, T. L., Beebe, N. W., Burkot, T. R., and Devine, G. J. (2022). A morphological key to the common mosquito species in the Pacific including medically important vectors. Retrieved from https://orene.org/wp-content/uploads/2024/01/PACMOS1.pdf. Accessed: 8/22/2025.
  21. Irikannu,K. C., Onyido, A. E., Umeanaeto, P. U., Onyebueke, A.C., Nzeukwu, C. I., Ogbonna, C. U., Ezeagwuna, D. A., Ogaraku, J. C., and Asogwa, K. K. (2021). Breeding ecology and physicochemical properties of mosquito breeding sites in Awka South Local Government Area, Anambra State, Nigeria. Trends in Entomology, 17: 35-42.
  22. Joseph, A. O., Adepeju, S-O, I., and Omosalewa, O. B. (2013). Distribution, abundance and diversity of mosquitoes in Akure, Ondo State, Nigeria. Journal of Parasitology and Vector Biology, 5(10): 132-136.
  23. Juliano, S. A., and Lounibos, L. P. (2005). Ecology of invasive mosquitoes: Effects on native communities. Annual Review of Entomology, 50, 77-97.
  24. Kermelita, D., Hadi, U. K., Soviana, S., Tiuria, R., and Supriyono, S. (2024). Species diversity of mosquitoes (Diptera: Culicidae), larval habitat characteristics, and potential as vectors for lymphatic filariasis in Central Bengkulu Regency, Indonesia. Veterinary World, 17(9): 2115–2123.
  25. Li, J., Docile, H. J., · Fisher, D., Pronyuk, K., and Zhao, L. (2024). Current Status of Malaria Control and Elimination in Africa: Epidemiology, Diagnosis, Treatment, Progress and Challenges. Journal of Epidemiology and Global Health, 14: 561–579. https://doi.org/10.1007/s44197-024-00228-2.
  26. Multini, L. C., Oliveira-Christe, R., Medeiros-Sousa, A., Evangelista, E., Barrio-Nuevo, K. M., Mucci, L. F., Ceretti-Junior, W., Camargo, A. A., Wilke, A. B. B., and Marrelli, M. T. (2021). The influence of pH and salinity of water in breeding sites on the occurrence and community composition of immature mosquitoes in the green belt of the city of Sao Paulo, Brazil. Insects, 12: 797. https://doi.org/10.3390/insects12090797.
  27. Obi, O. A., Nock, I. H., and Adebote, D. A. (2019). Biodiversity of Microinvertebrates coinhabiting mosquitoes habitats in patchy rock pools on inselbergs within Kaduna State, Nigeria. The Journal of Basic Zoology, 80: 57. https://doi.org/10.1186/s41936-019-0125-z.
  28. Ortega, J. C. G., Bruno R. S. Figueiredo, B. R. S., da Graça, W. J., Agostinho, A. A., and Bini. L. M. (2020). Negative effect of turbidity on prey capture both visual and non-visual aquatic predators. Journal of Animal Ecology, 89: 2427–2439.
  29. Prasadini, M., Dayananda, D., Fernando, S., Harischandra, I., and De Silva, N. (2019). Blood Feeding Preference of Female Aedes aegypti Mosquitoes for Human Blood Group Types and Its Impact on Their Fecundity: Implications for Vector Control. American Journal of Entomology, 3(2), 43-48.
  30. Robert, V., Goff, G. L., Ariey, F., and Duchemin, J. B. (2002). A possible alternative method for collecting mosquito larvae in rice fields. Malaria Journal, 1: 1-4.
  31. Russell, T. L., Staunton, K., and Burko, T. (2022). Standard Operating Procedure for collecting resting mosquitoes with pyrethrum spray catch. https://protocols.io/view/standard-operating-procedure-for-collecting-restin-b9mur46w.   Accessed: 10/24/2025.
  32. Sengil, A.Z., Akkaya, H., Gonenc, M., Gonenc, D. And Ozkan, D. (2011). Species composition and monthly distribution of mosquito (Culicidae) larvae in the Istanbul metropolitan area, Turkey. International Journal of Biological & Medical Research, 2(1), 415-424.
  33. WHO (2024b). World malaria report 2024: addressing inequity in the global malaria response. Geneva: World Health Organization; 2024. Licence: CC BY-NC-SA 3.0 IGO. Retrieved from https://creativecommons.org/licenses/by-nc-sa/3.0/igo). Access: 8/4/2025.
  34. WHO, (2013). Malaria Entomology and Vector Control Guide for Participants Training Module on Malaria Control. World Health Organization, Geneva, Switzerland. https://apps.who.int/iris/bitstream/handle/10665/85890/9789241505819_eng.pdf Accessed March 11. Accessed: 3/11/2021.
  35. WHO, (2024a). Regional data and trends briefing kit, world Malaria report 2024. Retrieved from file:///C:/Users/Daben/Desktop/world-malaria-report-2024-regional-briefing-kit-eng.pdf. Accessed: 10/22/2025.
  36. Wilke, A. B. B., Chase, C., Vasquez, C., Carvajal, A., Medina, J., Petrie, W. D., and Beier, J. C. (2019). Urbanization creates diverse aquatic habitats for immature mosquitoes in urban areas. Scientific Reports, 9:15335 | https://doi.org/10.1038/s41598-019-51787-5.
  37. Wilke, A. B. B., Chase, C., Vasquez, C., Carvajal, A., Medina, J., Petrie, W. D., and Beier, J. C. (2019). Urbanization creates diverse aquatic habitats for immature mosquitoes in urban areas. Scientific Reports, 9:15335 | https://doi.org/10.1038/s41598-019-51787-5.
  38. Wong, S. F., Chong, Y. L., and Yeo, F. K. S. (2024). Diversity of mosquito species (Diptera: Culicidae) in the residential area and rice field of Kampung Rembus, Samarahan Division, Sarawak, Malaysia. Serangga, 29(3), 267-280.
  39. Zhao, Z., Zung, J. L., Hinze, A., Kriete, A. L., Iqbal, A., Younger, M. A., Matthews, B. J., Merhof, D., Thiberge, S., Ignell, R., Strauch, M., and McBride, C. S. (2022). Mosquito brains encode unique features of human odour to drive host seeking. Nature, 605(7911): 706–712.

Mosquitoes are cosmopolitan and are mostly found in freshwater bodies such as ponds, drainages, sewages, stagnant and slow flowing rivers. The study investigated physicochemical parameters of rock-pool mosquito larval habitats of Amazah and species diversity of indoor-resting mosquitoes in Lamingo villages. Three sampling points (A, B and C) were randomly selected; and physicochemical parameters that include pH, temperature, dissolved oxygen (DO), total dissolved solids (TDS), conductivity, turbidity, salinity and depth were conducted. Adult mosquitoes were sampled from 30 households of nearby communities of the rock pool larval habitats, by pyrethrum spray. Mosquitoes collected, were identified using standard keys. The physicochemical properties results revealed significance difference (p ≤ 0.05) between Depth and TDS. Total of 252 larvae collected, belongs to Anopheline and Culicine group. Anopheles spp., were the most abundant 180, closely followed by Culex spp. (72) (t = 45.089, df = 2, p < 0.001). Anopheles larval mosquitoes spp., were commonly found in shallow pools with higher TDS levels; while Culex spp., were found in deeper pools. Anopheline species appear to prefer polluted and unclean water ponds. A total of 208 (f-ratio 14.8159. p = 0.0006) indoor-resting adult mosquitoes of nearby communities collected, belongs to 3 genera. Culex was the most dominant [RA = 47.11%; closely followed by Anopheles, RA = 44.23% and the least was Aedes, RA = 8.65%, diversity index (H) = 5.49]. The study concluded with greater health implications and the need for targeted vector control; which may involve proper environmental management strategies that can curtail prevalence of mosquito-borne diseases within the localities.

Keywords : Abundance, Diversity, Indoor-Resting, Mosquitoes, Physicochemical.

Paper Submission Last Date
31 - March - 2026

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