Open Access Open Access  Restricted Access Subscription Access

Studies on the Maintenance of 'Self-Sustained' Mosquito Vector Population in Vaigai River, South India


Affiliations
1 Department of Plant Sciences, Madurai Kamaraj University, Madurai-625 021, India
2 Centre for Research in Medical Entomology (ICMR), Madurai-625 002, India
 

Study of mosquito species diversity and its relationship with ecosystems is essential to understand disease epidemiology and to develop control measures of vector populations in human-dominated ecosystems. In the present study, the structure and composition of immature mosquito population and associated ecological parameters were analysed in three different ecosystems (urban, semi-urban and rural) along Vaigai river, Madurai, Tamil Nadu, India. Average larval density was higher in urban than the semi-urban and rural sites during the study period. In 2012-13, immature mosquito diversity was higher in rural site during pre-monsoon and monsoon seasons, whereas mosquito larval diversity was greater in semi-urban site during the post-monsoon season. In 2013-14, mosquito larval diversity was found to be high in semi-urban site during monsoon and post-monsoon seasons. Culicine species dominated the urban areas, while Anopheline species dominated the rural and semi-urban sites during the study period. Among the mosquito species, Culex tritaeniorhynchus, Cx. geldius, Cx. vishnuvi, Cx. quinquefasciatus, Cx. bitaeniorhynchus, Anopheles subpictus and An. culicifacies were prevalent throughout the year. Filamentous algal-dominated sites showed a higher number of mosquito species (23 species) than other hydrophytes-dominated sites. Maximum number of sewage inlets was recorded in urban than the other two sites. As a result, the highest turbidity level was recorded in the urban site followed by semi-urban and rural sites. The present study shows that the immature mosquito population is maintained with the help of ecological parameters in all the study sites throughout the year. Therefore, it is essential to take steps to eradicate the mosquito vectors from the Vaigai river basin to avoid disease outbreak in the region.

Keywords

Animal Husbandry, Aquatic Vegetation, Larval Density, Sewage Inlets, Water Quality.
User
Notifications
Font Size

  • Dudgeon, D. et al., Freshwater biodiversity: importance, threats, status and conservation challenges. Biol. Rev., 2006, 81, 163–182.
  • Doll, P., Fiedler, K. and Zhang, J., Global scale analysis of river flow alteration due to water withdrawals and reservoirs. Hydrol. Earth Syst. Sci., 2009, 13, 2413–2432.
  • CPCB, Water quality status and statistics (1993 and 1994): monitoring of Indian aquatic resources (MINARS/10/1995–1996), Central Pollution Control Board, New Delhi, 1996, p. 459.
  • Nilsson, C., Reidy, C. A., Dynesius, M. and Revenga, C., Fragmentation and flow regulation of the world’s largest river system. Science, 2005, 308, 405–408.
  • Balamurugan, C. and Leena Hebsibai, L., Studies on the pollution potential of Vaigai river at Madurai, India. Asian J. Res. Chem., 2012, 5, 1108–1112.
  • Rengasamy, R., Bridges-in-Vaigai-River, 2009; http://www.scribd. com/doc/11523096/Bridges-in-Vaigai-River
  • Jeyachandran, A., Krishnan, N. and Jeyakumar, G., Observations on the loss of biomass of Eichhornia crassipes in the river bed of Vaigai, Tamil Nadu. J. Ecobiol., 1994, 6, 153–155.
  • Jeyachandran, A., Krishnan, N. and Jeyakumar, G., Performances of Ipomoea cornea in river Vaigai in relation of pollution: a quantitative morphological study. J. Ecobiol., 1993, 5, 221–223.
  • Jeyachandran, A., Krishnan, N. and Jeyakumar, G., Further studies on plants in River Vaigai, South India in relation to pollution; performances of Eichhornia crassipes. Poll. Res., 1993, 12, 113– 115.
  • Roshinebegam, K., Selvakumar, S., Murugan, K. and Indumathi, R., Analysis of water quality in different sampling sites of Vaigai river, Tamil Nadu, India. J. Biosci. Res., 2013, 4, 46–53.
  • Krishnan, N. and Sujatha, T. R., A qualitative study on facial pollution by human defaecation in a south Indian river. In Ecology of Polluted Water Vol. II (ed. Arvind Kumar), APH Corporation, New Delhi, 2002, pp. 785–791.
  • Anandavalli, M., Water Pollution in Madurai: Yesterday, Publication Division, Madurai Kamaraj University, Madurai, 1986, p. 192.
  • Nabar, B. M., Shepaal, K. B., Lele, H. M. and Lokegaonkar, S. P., Statistical survey of mosquito vectors in the vicinity of Waldhun water body, District Thane – India. West African J. Appl. Ecol., 2011, 9, 139–149.
  • Pant, C. P., Vectors of Japanese encepalitis and their bionomics. WHO/VBC/79, 1979, 732, 1–18.
  • Mwangangi, J. M. et al., Anopheles larval abundance and diversity in three rice agro-village complexes Mwea irrigation scheme, Central Kenya. Malar. J., 2010, 9, 228–238.
  • Aditya, G., Premanik, M. K. and Saha, G. K., Larval habitats and species composition of mosquitoes in Darjeeling Himalayas, India. J. Vector. Borne Dis., 2006, 43, 7–15.
  • Sattler, M. A., Mtasiwa, D., Kiama, M., Premji, Z., Tanner, M., Killeen, G. F. and Lengeler, C., Habitat characterization and spatial distribution of Anopheles sp. mosquito larvae in Dares Salaam (Tanzania) during an extended dry period. Malar. J., 2005, 4, 4–18.
  • Blaustein, L. and Kotler, B. P., Oviposition habitat selection by the mosquito Culiseta longiareolata: effects of conspecifics, food and green toad tadpoles. Ecol. Entomol., 1993, 18, 104–108.
  • Angelon, K. A. and Petranka, J. W., Chemicals of predatory mosquitofish (Gambusia affinis) influence selection of oviposition site by Culex mosquitoes. J. Chem. Ecol., 2002, 28, 797–806.
  • Manda, H., Gouagna, L. C., Foster, W. A., Jackson, R. R., Beier, J. C., Githure, J. I. and Hassanali, A., Effect of discriminative plant-sugar feeding on the survival and fecundity of Anopheles gambiae. Malar. J., 2007, 6, 103–111.
  • Stone, C. M., Jackson, B. T. and Foster, W. A., Effects of plantcommunity composition on the vectorial capacity and fitness of the malaria mosquito Anopheles gambiae. Am. J. Trop. Med. Hyg., 2012, 87, 727–736.
  • Reuben, R., Thenmozhi, V., Samuel, P., Gajanana, A. and Mani, T., Mosquito blood feeding patterns as a factor in the epidemiology of Japanese encephalitis in southern India. Am. J. Trop. Med. Hyg., 1992, 46, 654–663.
  • Ejtehadi, H., Sepehri, A. and Akefi, H. R., Measuring Way of Biodiversity, Mashhad Ferdowsi Publications University, Mashhad, Iran, 2009, p. 229.
  • Pielou, E. C., The measurement of diversity in different types of biological collections. J. Theor. Biol., 1966, 13, 131–144.
  • Margalef, R., Temporal succession and spatial heterogeneity in phytoplankton. In Perspectives in Marine Biology (ed. BuzzatiTraverso), University of California Press, Berkeley, 1958, pp. 323–347.
  • Patz, J. A., Graczyk, T. K., Geller, N. and Vittor, A. Y., Effects of environmental change on emerging parasitic diseases. Int. J. Parasitol., 2000, 30, 1395–1405.
  • Gimnig, J. E., Ombok, M., Kamau, L. and Hawley, W. A., Characteristics of larval anopheline (Diptera: Culicidae) habitats in western Kenya. J. Med. Entomol., 2001, 38, 282–288.
  • Chinery, W. A., Effects of ecological changes on the malaria vectors Anopheles funestus and the Anopheles gambiae complex of mosquitoes in Accra, Ghana. J. Trop. Med. Hyg., 1984, 87, 75–81.
  • Guo, Q. H., Ma, K. M., Yang, L., Cai, Q. H. and He, K., A comparative study of the impact of species composition on a freshwater phytoplankton community using two contrasting biotic indices. Ecol. Indic., 2010, 10, 296–302.
  • Mapira, J. and Mungwini, P., River pollution in the city of Masvingo: a complex issue. Zambezia, 2005, 32, 95–106.
  • Cole, J. J., Findlay, S. and Pace, M. L., Bacterial production in fresh and saltwater ecosystems: a cross overview. Mar. Ecol. Prog. Ser., 1988, 43, 1–10.
  • Sunish, I. P. and Reuben, R., Factors influencing the abundance of Japanese encephalitis vectors in rice fields in India. II. Biotic. J. Med. Entomol., 2002, 16, 1–9.
  • Bond, J. G., Arredondo-Jimenez, J. I., Rodriguez, M. H., QuirozMartinez, H. and Willwams, T., Oviposition habitat selection for a predator refuge and food source in a mosquito. Ecol. Entomol., 2005, 30, 255–263.
  • Gimnig, J. E. et al., Density-dependant development of Anopheles gambiae (Diptera: Culicidae) larvae in artificial habitats. J. Med. Entomol., 2002, 39, 162–172.
  • Kant, R., Pandey, S. D. and Sharma, S. K., Mosquito breeding in relation to aquatic vegetation and some physico-chemical parameters in rice fields of central Gujarat. Indian J. Malariol., 1996, 33, 30–40.
  • Rejmankova, E. et al., Environmental and regional determinants of Anopheles (Diptera: Culicidae) larval distribution in Belize, Central America. Environ. Entomol., 1993, 22, 978–992.
  • Savage, H. M., Rejmankova, E., Arredondo Jimenez, J. I., Roberts, D. R. and Rodriguez, H., Limnological and botanical characterization of larval habitats for two primary malarial vectors, Anopheles albimanus and An. pseudopunctipennis, in coastal areas of Chiapas State, Mexico. J. Am. Mosq. Control Assoc., 1990, 6, 612–620.
  • Bond, J. G., Rojas, J. C., Arredondo-Jiménez, J. I., QuirozMartínez, H., Valle, J. and Williams, T., Population control of the malaria vector Anopheles pseudopunctipennis by habitat manipulation. Proc. R. Soc. London, Ser. B, 2004, 271, 2161–2169.
  • Femandez-Salas, I., Roberts, D. R., Rodriguez, M. H. and MarinaFernandez, C., Bionomics of larval populations of Anopheles pseudopunctipennis in the Tapachula foothills area, southern Mexico. J. Am. Mosq. Control. Assoc., 1994, 10, 477–486.
  • Opoku, A. A., Ansa-Asare, O. D. and Amoako, J., The occurrences and habitat characteristics of mosquitoes in Accra, Ghana. West Afr. J. Appl. Ecol., 2007, 11, 81–86.
  • Walton, W. E., Schreiber, E. T. and Mulla, M. S., Distribution of Culex tarsalis larvae in a freshwater marsh in Orange County, California. J. Am. Mosq. Control Assoc., 1990, 6, 539–543.
  • Greenway, M., Suitability of macrophytes for nutrient removal from surface flow constructed wetlands receiving secondary treated effluent in Queensland, Australia. Water Sci. Technol., 2003, 48, 121–128.
  • Mutuku, F. M. et al., A supervised land cover classification of a western Kenya lowland endemic for human malaria: associations of land cover with larval Anopheles habitats. Int. J. Health Geogr., 2009, 8, 19–31.
  • Bhattacharyya, D. R. et al., Host feeding patterns of Culex vishnui sub group of mosquitoes in Dibrugarh district of Assam. J. Commun. Dis., 1994, 26, 133–138.
  • Arunachalam, N., Samuel, P. P., Hiriyan, J., Thenmozhi, V. and Gajanana, A., Japanese encephalitis in Kerala, South India: can Mansonia (Diptera: Culicidae) play a supplemental role in transmission? J. Med. Entomol., 2004, 41, 456–461.
  • Zinser, M., Ramberg, F. and Willott, E., Culex quinquefasciatus (Diptera: Culicidae) as a potential West Nile virus vector in Tucson, Arizona: blood meal analysis indicates feeding on both humans and birds. J. Insect Sci., 2004, 4, 1–3.
  • Hasegawa, M., Tuno, N., Yen, N. T., Nam, V. S. and Takagi, M., Influence of the distribution of host species on adult abundance of Japanese encephalitis vectors Culex vishnui subgroup and Culex gelidus in a rice-cultivating village in northern Vietnam. Am. J. Trop. Med. Hyg., 2008, 78, 159–168.

Abstract Views: 485

PDF Views: 103




  • Studies on the Maintenance of 'Self-Sustained' Mosquito Vector Population in Vaigai River, South India

Abstract Views: 485  |  PDF Views: 103

Authors

N. Kamaladhasan
Department of Plant Sciences, Madurai Kamaraj University, Madurai-625 021, India
B. K. Tyagi
Centre for Research in Medical Entomology (ICMR), Madurai-625 002, India
P. S. Swamy
Department of Plant Sciences, Madurai Kamaraj University, Madurai-625 021, India
S. Chandrasekaran
Department of Plant Sciences, Madurai Kamaraj University, Madurai-625 021, India

Abstract


Study of mosquito species diversity and its relationship with ecosystems is essential to understand disease epidemiology and to develop control measures of vector populations in human-dominated ecosystems. In the present study, the structure and composition of immature mosquito population and associated ecological parameters were analysed in three different ecosystems (urban, semi-urban and rural) along Vaigai river, Madurai, Tamil Nadu, India. Average larval density was higher in urban than the semi-urban and rural sites during the study period. In 2012-13, immature mosquito diversity was higher in rural site during pre-monsoon and monsoon seasons, whereas mosquito larval diversity was greater in semi-urban site during the post-monsoon season. In 2013-14, mosquito larval diversity was found to be high in semi-urban site during monsoon and post-monsoon seasons. Culicine species dominated the urban areas, while Anopheline species dominated the rural and semi-urban sites during the study period. Among the mosquito species, Culex tritaeniorhynchus, Cx. geldius, Cx. vishnuvi, Cx. quinquefasciatus, Cx. bitaeniorhynchus, Anopheles subpictus and An. culicifacies were prevalent throughout the year. Filamentous algal-dominated sites showed a higher number of mosquito species (23 species) than other hydrophytes-dominated sites. Maximum number of sewage inlets was recorded in urban than the other two sites. As a result, the highest turbidity level was recorded in the urban site followed by semi-urban and rural sites. The present study shows that the immature mosquito population is maintained with the help of ecological parameters in all the study sites throughout the year. Therefore, it is essential to take steps to eradicate the mosquito vectors from the Vaigai river basin to avoid disease outbreak in the region.

Keywords


Animal Husbandry, Aquatic Vegetation, Larval Density, Sewage Inlets, Water Quality.

References





DOI: https://doi.org/10.18520/cs%2Fv110%2Fi1%2F57-68