Abstract
Aquatic temperature influences the development and survival of immature Anopheles stephensi with implications for vector population trends and control strategies under climate change. Temperature was recorded from breeding habitats in Besant Nagar, Chennai, using floatable data loggers, in cemented overhead tank (cOHT), synthetic overhead tank (sOHT), shaded-well (S-Well) and non-shaded well (NS-Well). Hourly temperatures were analyzed across months and seasons. Immature survivorship experiments were carried out in biological incubators simulating habitat temperatures and compared with standard conditions. Adult mosquito longevity was assessed under simulated thatched-roof temperatures. sOHT recorded the highest temperatures, followed by cOHT, with wells recording minimum temperatures. Kruskal-Wallis tests showed significant differences in Hatching rate (HR) and Pupation rate (PR) across habitat temperatures, but not in Emergence rate (ER). Dunn’s analysis revealed better immature development under Standard and Well conditions versus cOHT and sOHT. PERMANOVA confirmed temperature’s strong influence on development, with cOHT causing the greatest survivorship variation. Adults emerging under cOHT conditions showed higher longevity than sOHT, while the adults which emerged from wells survived longest. This study demonstrates habitat-specific thermal effects on An. stephensi development and survival. Vector control through habitat modification, preventing breeding in overhead tanks, and public awareness are crucial for urban malaria elimination.
Similar content being viewed by others
Data availability
All data supporting the findings of this study, including analyzed data and supplementary files, are included in this manuscript.
References
Martens, W. J. M., Niessen, L. W., Rotmans, J. & McMichael, A. J. Potential impact of global climate change on malaria risk. Environ. Health Perspect. 103, 458–464 (1995).
Cella, W. et al. Do climate changes alter the distribution and transmission of malaria? Evidence assessment and recommendations for future studies. Rev. Soc. Bras. Med. Trop. 52, e20190308 (2019).
Murdock, C. C., Sternberg, E. D. & Thomas, M. B. Malaria transmission potential could be reduced with current and future climate change. Sci. Rep. 6, 27771 (2016).
World Malaria Report. https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2024 (2024).
Thomas, S. et al. Overhead tank is the potential breeding habitat of Anopheles stephensi in an urban transmission setting of Chennai, India. Malar. J. 15, 274 (2016).
Thomas, S. et al. Resting and feeding preferences of Anopheles stephensi in an urban setting, perennial for malaria. Malar. J. 16, 111 (2017).
National Centre for Vector Borne Diseases. Control (NCVBDC). https://ncvbdc.mohfw.gov.in/ (2025).
Health & Family Welfare Department. Government of Tamil Nadu. https://tnhealth.tn.gov.in/ (2025).
Mathanga, D. P. et al. Patterns and determinants of malaria risk in urban and peri-urban areas of Blantyre, Malawi. Malar. J. 15, 590 (2016).
Abram, P. K., Boivin, G., Moiroux, J. & Brodeur, J. Behavioural effects of temperature on ectothermic animals: unifying thermal physiology and behavioural plasticity. Biol. Rev. 92, 1859–1876 (2017).
Cator, L. J. et al. Characterizing microclimate in urban malaria transmission settings: a case study from Chennai, India. Malar. J. 12, 84 (2013).
Thomas, S. et al. Microclimate variables of the ambient environment deliver the actual estimates of the extrinsic incubation period of Plasmodium Vivax and Plasmodium falciparum: a study from a malaria-endemic urban setting, Chennai in India. Malar. J. 17, 201 (2018).
Lyimo, E. O., Takken, W. & Koella, J. C. Effect of rearing temperature and larval density on larval survival, age at pupation and adult size of Anopheles Gambiae. Entomol. Exp. Appl. 63, 265–271 (1992).
Beck-Johnson, L. M. et al. The effect of temperature on Anopheles mosquito population dynamics and the potential for malaria transmission. PLoS ONE. 8, e79276 (2013).
Christiansen-Jucht, C., Parham, P. E., Saddler, A., Koella, J. C. & Basáñez, M. G. Temperature during larval development and adult maintenance influences the survival of Anopheles Gambiae s.s. Parasite Vectors. 7, 1–10 (2014).
Paaijmans, K. P., Takken, W., Githeko, A. K. & Jacobs, A. F. G. The effect of water turbidity on the near-surface water temperature of larval habitats of the malaria mosquito Anopheles Gambiae. Int. J. Biometeorol. 52, 747–753 (2008).
Thomas, S. et al. Does fluoride influence oviposition of Anopheles stephensi in stored water habitats in an urban setting? Malar. J. 15, 549 (2016).
Kumar, D. S., Andimuthu, R., Rajan, R. & Venkatesan, M. S. Spatial trend, environmental and socioeconomic factors associated with malaria prevalence in Chennai. Malar. J. 13, 14 (2014).
Mattah, P. A. D. et al. Diversity in breeding sites and distribution of Anopheles mosquitoes in selected urban areas of Southern Ghana. Parasit. Vectors. 10, 25 (2017).
Carter, T. E. et al. First detection of Anopheles stephensi Liston, 1901 (Diptera: culicidae) in Ethiopia using molecular and morphological approaches. Acta Trop. 188, 180–186 (2018).
Balkew, M. et al. Geographical distribution of Anopheles stephensi in Eastern Ethiopia. Parasit. Vectors. 13, 35 (2020).
Surendran, S. N. et al. Molecular characterization and identification of members of the Anopheles subpictus complex in Sri Lanka. Malar. J. 12, 304 (2013).
Abubakr, M. et al. The phylodynamic and spread of the invasive Asian malaria Vectors, Anopheles stephensi, in Sudan. Biology 11, 409 (2022).
Singh, H., Gupta, S. K., Vikram, K., Saxena, R. & Sharma, A. The impact of mosquito proof lids of underground tanks Tanka on the breeding of Anopheles stephensi in a village in Western Rajasthan, India. Malar. J. 20, 412 (2021).
Agyekum, T. P. et al. A systematic review of the effects of temperature on Anopheles mosquito development and survival: implications for malaria control in a future warmer climate. Int. J. Environ. Res. Public. Health. 18, 7255 (2021).
George, L. et al. Community-Effectiveness of temephos for dengue vector control: a systematic literature review. PLoS Negl. Trop. Dis. 9, e0004006 (2015).
Mishra, R. et al. Managing malaria: a scourge on the South East Coast. Curr. Sci. 121, 00113891 (2021).
Van Eijk, A. M. et al. The burden of submicroscopic and asymptomatic malaria in India revealed from epidemiology studies at three varied transmission sites in India. Sci. Rep. 9, 145 (2019).
Nagpal, B. N., & Sharma, V. P. Indian Anophelines (Science Publishers, Inc. 1995).
Nagpal, B. N. Pictorial Identification Key for Indian Anophelines (Malaria Research Centre (ICMR), 2005).
Ravishankaran, S. et al. Does the roof type of a house influence the presence of adult Anopheles stephensi, urban malaria vector? – evidence from a few slum settings in Chennai, India. Parasitol. Res. 121, 105–114 (2022).
Ravishankaran, S. et al. Influence of household roof types on the development of Plasmodium Vivax in Anopheles stephensi mosquitoes. Am. J. Trop. Med. Hyg. 112, 286–295 (2025).
Sharma, P., Mohan, L. & Srivastava, C. N. Phytoextract-induced developmental deformities in malaria vector. Bioresour Technol. 97, 1599–1604 (2006).
Ngowo, H. S., Hape, E. E., Matthiopoulos, J., Ferguson, H. M. & Okumu, F. O. Fitness characteristics of the malaria vector Anopheles funestus during an attempted laboratory colonization. Malar. J. 20, 148 (2021).
NASA POWER. Prediction of Worldwide Energy Resources (POWER) https://power.larc.nasa.gov/ (2025).
Garamszegi, L. Z. et al. Changing philosophies and tools for statistical inferences in behavioral ecology. Behav. Ecol. 20, 1363–1375 (2009).
Thomas, S. et al. Socio-demographic and household attributes may not necessarily influence malaria: evidence from a cross-sectional study of households in an urban slum setting of Chennai, India. Malar. J. 17, 4 (2018).
Oliver, S. V. & Brooke, B. D. The effect of elevated temperatures on the life history and insecticide resistance phenotype of the major malaria vector Anopheles arabiensis (Diptera: Culicidae). Malar. J. 16, 73 (2017).
O.D., M. Effects of temperature and relative humidity on the development of Anopheles mosquitoes reared in the laboratory. Afr J. Nat. Sci. AJNS (2025).
Atieli, H. E. et al. Insecticide-treated net (ITN) ownership, usage, and malaria transmission in the highlands of Western Kenya. Parasit. Vectors. 4, 113 (2011).
Bhattacharyya, B. & Bordoloi, J. P. Effect of three different roofing materials on milk production of Jersey grade cows in different seasons: a field study in Guwahati. Res. J. Anim. Veterinary Fish. Sci. 3 (9), 1–4 (2015).
Stresman, G. H. Beyond temperature and precipitation: ecological risk factors that modify malaria transmission. Acta Trop. 116, 167–172 (2010).
Yates, W. W. Effect of temperature on the insecticldal action of mosquito larvicides. Mosq. News. 10 (4), 202–204 (1950).
Paaijmans, K. P., Wandago, M. O., Githeko, A. K. & Takken, W. Unexpected high losses of Anopheles Gambiae larvae due to rainfall. PLoS ONE. 2, e1146 (2007).
Yoshioka, M. et al. Diet and density dependent competition affect larval performance and oviposition site selection in the mosquito species Aedes albopictus (Diptera: Culicidae). Parasit. Vectors. 5, 225 (2012).
Abbasi, M. et al. The impact of Climatic variables on the population dynamics of the main malaria vector, Anopheles stephensi liston (Diptera: Culicidae), in Southern Iran. Asian Pac. J. Trop. Med. 13, 448 (2020).
Liu, Z. et al. Effect of temperature and its interactions with relative humidity and rainfall on malaria in a temperate City Suzhou, China. Environ. Sci. Pollut Res. 28, 16830–16842 (2021).
Acknowledgements
We thank the Indian Council of Medical Research and National Institute of Malaria Research for providing the necessary facilities and support. We gratefully acknowledge Mr. E. Elumalai for the help rendered in the field work and all other staff of the NIMR field unit of Chennai for their valuable support. We express our sincere gratitude to the community of Besant Nagar for permitting us to place the temperature data loggers for a year. We also thank Prof. Jane Carlton for her invaluable support and suggestions during the study period and Dr. Lalitha Ramanathapuram for the procurement of the data loggers and other support. The financial assistance of ICMR (Senior Research Fellowship), New Delhi, to Dr. Sangamithra Ravishankaran for this study is thankfully acknowledged.
Funding
This work was supported by the National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH) Grant U19AI089676, an International Center of Excellence for Malaria Research. The content of this manuscript is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Author information
Authors and Affiliations
Contributions
AE conceptualised and designed the study, oversaw its implementation and reviewed the manuscript. SR wrote the manuscript, performed data cleaning, statistical analysis and visualizations. JAJ, AA, ST, SR carried out the field work involving installation of the data loggers and subsequent fortnightly downloads, and adult vector collection. They also carried out the immature survivorship experiments. AA, KPK, and TS contributed to data analysis and edited the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Ethical approval
Clearance to conduct the scientific study was approved by the Scientific Advisory Committee of ICMR-National Institute of Malaria Research, New Delhi (NIMR/PB/2010/150) and the institutional ethical clearance of the study was also obtained from ICMR- National Institute of Malaria Research of the Indian Council of Medical Research, New Delhi (ECR/NIMR/EC/2010/100).
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Ravishankaran, S., Asokan, A., Kripa, P.K. et al. Thermal dynamics of vector breeding habitats and their impact on immature survivorship of Anopheles stephensi in Chennai, India. Sci Rep (2026). https://doi.org/10.1038/s41598-026-35819-5
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-026-35819-5


