In the study of diptera diversity and distribuiton conducted in 2020-2021 we found insect species in 23 families out of 64 common individual species. Site-A Hidden Valley is considered to be the place with the highest number of individual (861nos). In this study we found that most pollination in the Nilgiris in the diptera order is done on small flowering plants. Fruit fly insect are never harmful to the fruits of the Nilgiris eg- Rhagoletis sp. Stomoxys sp, Musca sp species of insect found mostly in cattle and gaur in the Nilgiris The study was conducted in four different forest areas in the Nilgiris and in the lake area, Ooty Lake is the most associated area for humans and flies. This study is not only about this period but also about the future studies of these insects mostly because they are important for all types of ecological environment.
Keywords:Diptera, Diversity, Pollination, Environment, Nilgiris, Westernghats.
Received: 18 February 2022 / Revised: 1 April 2022 / Accepted: 15 April 2022/ Published: 6 May 2022
This study will be an important study to identify diptera species in the nilgiris and to continue further research on these insects in the future. Because studies on diptera are not much in the westernghats.
The order Diptera is one of the largest insect orders in the world. In the order documented 2,70,219 species worldwide, under 150 families [1]. Some diptera families are both beneficial and harmful to natural with human environment most flies are diurnal and may visit flower for nector include some species of syrphidae, Bombylidae and culucidae calliphora vicina more than 500 flies per week per day is an efficient and cost-effective pollinator for scale production [2]. While numerous others feed upon decaying organic matter and diverse third substances. Several groups of flies are predators on smaller insects or parasitoids as larva and adults including Asilidae, Empididae, Dolicophodidae, Syrphidae and Tachinidae. Some are found in decomposing organic substance and some groups play a major role in forensic entomology. Many dipterans are blood suckers and are harmful to humans and animals and cause economic losses. Mosquitoes are important as vectors of several tropical diseases including malaria, filariases, dengue, Japanese encephalitis and yellow fever. In temperate countries, mosquitoes and biting midges are nuisance pests than vectors. In India, fruit crops such as mango and guava suffer great economic yield losses due to the Oriental fruit fly, Bactocera dorsalis [3]. Hepatitis B is transmitted by Chrysops sp. (Family Tabanidae) and many people have been affected by this pathogen [4]. Research has been done on mosquitoes in the Nilgiri hills, but studies on other dipteran insects in the Nilgiris have not been extensive [5-10]. The Nilgiris Range boasts of a diverse array of flora and fauna, including unique wildlife and there is an important relationship between flies and animals.
This study was conducted in the Nilgiri hills covering a range of habitats such as margin of the mountain rain forest, shola forest, grass lands, lake, and endangered shola forest in the year 2020-2021. Four locations with geographical and climatical differences were studied and surveys were conducted four days a month in a year. Specimens were collected only photographs various location with a Nikon P900 camera. GPS locations were recorded with the help of Garmin GPS Location device. We identified the species with the help of key studies and books [11, 12]. The numbers of flies on the flowers, grasses, leaves and animal faeces in all seasons were counted. Study Methods: two types of calculation was conducted in the study diversity calculated on the basis of individual families, and basis of species diversity collected from four locations. Shannon-Weiner index (H’) [13] Simpson diversity index (D) [14] Margalefe index (Dmg) [15] Pielou Evenness (J’) [16]. We compiled the results of the study using these Calculation.
Figure 1. Shows the diversity indices for Diptera in Hidden Valley study site
Figure 2. Shows the diversity indices for Diptera in Valley View study site.
Figure 3. Shows the diversity indices for Diptera in Ooty Lake study site.
Figure 4. Shows the diversity indices for Diptera in Endangered shola forest study site.
2.1. Study Area
2.1.1. Site-A Coonoor – Hidden Valley
This forest area in the Coonoor range belongs to the mountain rain forest type (Lat: 11°22’07 Long: 76°47’47 Figure 5, which is a water rich area. Totally 0.76 km2 forest area has been surveyed. The region receives an annual rainfall of 70.8 inch and annual temperature is 21°C. This area is rich in wild, endemic and endangered flora and fauna.
2.1.2. Site-B Valley View
This forest is a rocky part of the mountain range (Lat: 11°23’31 Long: 76°43’23 Figure 5) with a mixture of grassy shola forest and forest plantation rich with wild, endemic and endangered flora and fauna. Totally 0.89 km2 Forest has been surveyed. The region receives an annual rainfall of 40.98 inch. Annual temperature is 17°C.
2.1.3. Site-C Ooty Lake
Ooty Lake (Lat: 11°24’90 Long: 76°41’21 (Figure 5)) is a man-made lake built by John Sullivan. The area around the lake is covered with plastic wastes, aquatic plants and sediments and also a grazing area for cattle. The lake is owned by the state tourism and fisheries department. Totally km2 area around the lake was surveyed. The region receives an annual rainfall 40.98 inch. Annual temperature is 17°C.
Figure 5. Localities surveyed in the Nilgiri hills.
2.1.4. Site-D Endangered Shola Forest Patch
This area is a small endangered shola forest (Lat: 11°23’20 Long: 76°42’11(Figure 5)) in the middle of the forest plantation in Lovedale town and it is frequented by cattle, deer and wild gaur. Totally 3.37 ha forest was surveyed. The region receives an annual rainfall of 59.6 inch. Annual temperature is 17°C.
In the study we recorded 2581 individuals belonging to 64 species in 23 families of the Order Diptera order commonly found in the Nilgiris and the Diversity Indices at the four locations are listed Table 1.
Table 1. Diversity indices for Diptera collected from four locations.
Calculation |
Site-A Hidden Valley |
Site-B Valley View |
Site-C Ooty Lake |
Site-D Endangered Shola Forest |
Dominance_D |
0.152 |
0.132 |
0.150 |
0.137 |
Simpson_1-D |
0.847 |
0.868 |
0.849 |
0.862 |
Shannon_H |
2.468 |
2.527 |
2.483 |
2.494 |
Evenness_e^H/S |
0.512 |
0.544 |
0.520 |
0.526 |
Margalef |
3.255 |
3.351 |
3.422 |
3.687 |
Individuals |
861 |
710 |
620 |
390 |
Figure 6. Diptera collected and identified in the study.
Note: 1. Episyrphus, 2. Lauxaniidae, 3. Lispe, 4. Muscidae, 5. Dolicopodidae, 6. Asarkina, 7. Bibionidae, 8. Sciaridae, 9. Anthomyiidae, 10. Stomoxys, 11. Dolicopodidae, 12. Tachinidae, 13. Phaonia, 14. Haematopota, 15. Asilidae, 16. Tabanus, 17. Gonia, 18. Nephrotoma, 19. Pselliophora laeta, 20. Dolicopodidae, 21. Chrysopilus, 22. Anthomyiidae, 23. Eristalinus arvorum, 24. Campiglossa product, 25. Haematopota, 26. Eriocera nepalensis, 27. Stratiomyidae, 28. Tipulidae, 29. Tipulidae, 30. Episyrphus, 31. Argyra, 32. Keroplatidae, 33. Muscidae, 34. Muscidae, 35. Morellia, 36. Muscoidea, 37. Prosena, 38. Sciaridae, 39. Stomoxys calcitrans, 40. Sarcophagidae, 41. Psychodidae, 42. Dexiinae, 43. Athericidae, 43. Neomyia, 44. Rhiniidae, 45.Tipulidae. 46. Hybotidae,47. Zaprionus, 48. Drosophila ananassae, 49. Baccha sp., 50. Bibio sp., 51. Asilidae, 52. Musca domestica, 53. Sarginae, 54. Tabanidae, 55. Bombyliidae, 56. Lucilia, 57. Tabanus, 58. Rhagoletis cingulata, 59. Asilidae, 60. Tachinidae, 61. Melanostoma mellinum, 62. Rioxoptilona inermis.
The images of 62 flies are featured in Figure 6. The Diptera fauna of the study area were indication good diversity index. Site-A Hidden Valley recorded the highest number of individuals (861nos) but with the lowest diversity index (>2.468) (Figure 1). Site-D Endangered Shola forest yielded the least number of individuals (390 nos) but had a high diversity and the diversity value was >2.527. Site-B also had the highest Simpson Diversity Index of >0.868 (Figure 2). The next highest diversity was found at Site-D (Diversity index ˃2.494) (Figure 4) which had the least individual counts. Site-C Ooty Lake third had the highest diversity (diversity index ˃2.483) (Figure 3). The site with the lowest diversity index value (˃2.468) had the highest individual counts. The Diversity Indices were also calculated on the basis of individual families (Table 2).
The highest number was found at Site-D (margalef index rate >3.687). Excessive evenness was seen at site-B with a Pielou evenness index of >0.5443. Shannon diversity, Margaliefs and Pielous evenness indices for the dipteran fauna of the study area were 2.953, 2.949 and 0.896, respectively, indicating their good diversity and richness [17]. Mumbai Metropolitan Region is represented by 57% (n=50) of family-level diversity of Diptera in India [18]. We found 41332 flies based on direct evidence, which is important for other inferences on the conservation of natural tropical and non-tropical environments in the world [19].
Table 2. Diversity indices calculated on the basis of individual families.
Diptera Family Name |
Common Names |
Margalefe index (Dmg) |
Simpson diversity index (D) |
Shanon-Weiner index (H’) |
Pielou Evenness (J’) |
Anthomyiidae |
Root-maggot flies |
0.581 |
0.503 |
1.034 |
0.431 |
Asilidae |
Robber flies |
0.461 |
0.247 |
0.531 |
0.242 |
Athericidae |
Athericid flies |
0.582 |
0.241 |
0.523 |
0.218 |
Bombyliidae |
Bee flies |
0.461 |
0.131 |
0.320 |
0.146 |
Bibionidae |
Fever flies |
0.574 |
0.227 |
0.535 |
0.223 |
Calliphoridae |
Blow flies |
0.587 |
0.189 |
0.455 |
0.189 |
Dolicophodiae |
Long legged flies |
0.491 |
0.142 |
0.348 |
0.158 |
Drosophilidae |
Small fruit flies |
0.593 |
0.381 |
0.882 |
0.368 |
Hybotidae |
Dance flies |
0.788 |
0.653 |
1.165 |
0.840 |
Keroplatidae |
Fungus gnats |
1.136 |
0.780 |
1.333 |
0.962 |
Lauxaniidae |
Lauxaniid flies |
0.697 |
0.666 |
1.187 |
0.856 |
Muscidae |
House flies |
0.444 |
0.729 |
1.341 |
0.967 |
Mycetophilidae |
Fungus gnats |
0.882 |
0.751 |
1.340 |
0.967 |
Rhagionidae |
Snipe flies |
0.644 |
0.682 |
1.249 |
0.901 |
Rhiniidae |
Blow flies |
0.890 |
0.716 |
1.266 |
0.913 |
Sarcophagidae |
Flash flies |
0.910 |
0.660 |
1.166 |
0.841 |
Sciaridae |
Fungus gnats |
0.824 |
0.741 |
1.325 |
0.956 |
Syrphidae |
Flower flies |
0.558 |
0.700 |
1.248 |
0.900 |
Stratiomyidae |
Soldier flies |
0.713 |
0.695 |
1.218 |
0.878 |
Tachinidae |
Tachinid flies |
0.609 |
0.700 |
1.267 |
0.914 |
Tephritoidea |
Fruit Flies |
0.824 |
0.701 |
1.240 |
0.894 |
Tabanidae |
Horse flies |
0.648 |
0.728 |
1.333 |
0.961 |
Tipulidae |
Crane flies |
0.593 |
0.749 |
1.375 |
0.992 |
Table 3. Diptera feeding habitat using flowers and decaying materials.
S.No |
Diptera Names |
Flora and other Materials |
Decaying Fauna |
|||||||||||||||
Tagetes erecta |
Bidens pilosa |
Cynoglossum Zeylanicum |
Justicia simplex |
Nicandra physalodes |
Euphorbia helioscopia |
Fruits |
Flies Predatory |
Blood Sucking |
Decaying wood/plants/mud |
wild Gaur Defecat |
Leopard Defecat |
Domestic Cattle Defecat |
BirdsDefecat |
Monkey Defecat |
WildCats Defecat |
|||
1 |
Condylostylus |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||||
2 |
Syrphidae |
• |
• |
• |
• |
• |
• |
• |
||||||||||
3 |
Gonia sp. |
• |
• |
• |
• |
• |
• |
|||||||||||
4 |
Rioxoptilona inermis |
• |
• |
|||||||||||||||
5 |
Tabanus sp. |
• |
• |
• |
• |
• |
• |
|||||||||||
6 |
Asilidae |
• |
• |
• |
• |
|||||||||||||
7 |
Tachinidae: Dexiinae |
• |
• |
• |
• |
• |
• |
|||||||||||
8 |
Melanostoma |
• |
• |
• |
• |
• |
• |
• |
||||||||||
9 |
Mydaea |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||||
10 |
Chrysotoxum sp. |
• |
• |
• |
• |
• |
||||||||||||
11 |
Tachinidae |
• |
• |
• |
• |
• |
• |
• |
||||||||||
12 |
Tabanus cf striatus |
• |
• |
• |
• |
• |
• |
|||||||||||
13 |
Bengalia sp. |
• |
• |
• |
• |
• |
• |
• |
||||||||||
14 |
Lucilia sp. |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||
15 |
Sargus sp. |
• |
• |
• |
• |
• |
||||||||||||
16 |
Haematopota |
• |
• |
|||||||||||||||
17 |
Chrysomya megacephala |
• |
• |
• |
• |
• |
• |
• |
||||||||||
18 |
Rhagionidae |
• |
• |
• |
• |
|||||||||||||
19 |
Melinda sp. |
• |
• |
• |
• |
|||||||||||||
20 |
Anthomyia sp. |
• |
• |
• |
• |
• |
• |
• |
• |
• |
||||||||
21 |
Amblypsilopus sp. |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||||
22 |
Condylastylus sp. |
• |
• |
• |
• |
• |
• |
• |
||||||||||
23 |
Dasysyrphus sp. |
• |
• |
• |
||||||||||||||
24 |
Stomoxys sp. |
• |
• |
• |
• |
• |
||||||||||||
25 |
Dexiinae |
• |
• |
• |
• |
• |
||||||||||||
26 |
Phaonia sp. |
• |
• |
• |
• |
• |
• |
|||||||||||
27 |
Nephrotoma sp. |
• |
||||||||||||||||
28 |
Pselliophora laeta |
• |
||||||||||||||||
29 |
Musca domestica |
• |
• |
• |
||||||||||||||
30 |
Bombyliidae |
• |
• |
• |
• |
• |
• |
• |
||||||||||
31 |
Rhagoletis cingulata |
• |
||||||||||||||||
32 |
Eriocera nepalensis |
• |
||||||||||||||||
33 |
Anthomyiidae |
• |
• |
• |
• |
• |
• |
• |
||||||||||
34 |
Bibionidae |
• |
• |
• |
• |
• |
• |
|||||||||||
35 |
Sciaridae |
• |
• |
• |
||||||||||||||
36 |
Chrysopilus sp. |
• |
• |
• |
• |
|||||||||||||
37 |
Asarkina sp. |
• |
• |
• |
• |
• |
• |
|||||||||||
38 |
Lauxaniidae (Homoneura sp.) |
• |
• |
• |
• |
• |
• |
|||||||||||
39 |
Muscidae |
• |
• |
• |
• |
• |
• |
|||||||||||
40 |
Bibio sp. |
• |
• |
• |
• |
|||||||||||||
41 |
Lispe sp. |
• |
• |
• |
• |
|||||||||||||
42 |
Episyrphus sp. |
• |
• |
• |
• |
• |
• |
• |
||||||||||
43 |
Rhagionidae |
• |
• |
• |
||||||||||||||
44 |
Baccha sp. |
• |
• |
• |
• |
• |
||||||||||||
45 |
Drosophila ananassae |
• |
• |
• |
||||||||||||||
46 |
Zaprionus sp. |
• |
• |
• |
• |
|||||||||||||
47 |
Hybotidae |
• |
• |
|||||||||||||||
48 |
Rhiniidae |
• |
• |
• |
• |
|||||||||||||
49 |
Neomyia sp. |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
||||
50 |
Athericidae |
• |
• |
• |
• |
|||||||||||||
51 |
Morellia sp. |
• |
• |
• |
• |
• |
• |
|||||||||||
52 |
Sarcophagidae |
• |
• |
• |
• |
• |
• |
• |
||||||||||
53 |
Dexiinae (Trichodura) |
• |
• |
• |
||||||||||||||
54 |
Musca sp. |
• |
• |
• |
• |
• |
||||||||||||
55 |
Muscidae sp. |
• |
• |
• |
• |
|||||||||||||
56 |
Muscoidea |
• |
• |
• |
• |
|||||||||||||
57 |
Prosena sp. |
• |
• |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||
58 |
Limoniidae |
• |
||||||||||||||||
59 |
Stomoxys calcitrans |
• |
• |
• |
• |
• |
• |
• |
• |
|||||||||
60 |
Sciaridae |
• |
• |
|||||||||||||||
61 |
Neoempheria sp. |
• |
• |
|||||||||||||||
62 |
Keroplatidae |
• |
• |
|||||||||||||||
63 |
Tipulidae |
• |
||||||||||||||||
64 |
Psychodidae |
• |
In this study, we have documented the habitat and food habits of 64 individuals (Table 3). Most Diptera species are seen during the winter and post-winter seasons. In this study we found 6 out of 47 species of Diptera were found on six types of flowering plants and most of these Diptera species used these flowering plants. Syrphidae, Melanostoma, Lucilia sp., Amblypsilopus, Condylastylus sp., Bombyliidae, Asarkina sp., Neomyia sp., and Prosena sp. were more common on the flowering plants which play an important role in pollination. Among all flower-visiting flies, the family Syrphidae with approximately 6000 species and 300 genera plays an important role in pollination [20]. Syrphids also act as alternative pollinators in the higher elevation landscapes of Himachal Pradesh [21]. Of the 14 families recorded study the family syrphidae having the highest number of species [22]. Syrphidae is the dominant group among the flower visiting flies of India [23]. 357 species of hover flies, more than 100 species are restricted in India. In Tamil Nadu (14.5%) widespread [24]. 21 Insect species are fruit bearing species. Rioxoptilona inermis this species was first spotted in the Nilgiris in this study and is a fruit-bearing species. Anthomyia sp, Condylastylus sp, Musca domestica, Rhagolets Cingulata, Drosophila ananassae, are the most abundant Nilgiri fruit suckers. Indicating a differential effect of density on the pollination efficiency of M. domestica and Calliphora vicina the linear trend for fly density and nonparallel regressions for the effect of fly species on seed yield per cage were significant [2]. Some species prey on small insects or their own species, in this study we observed four predatory species there are Asilidae,Hybotidae, Anthomyia sp., and Bengalia sp. A total of 6 species of blood-sucking Diptera order are commonly found in cows and domestic dogs Haematopota sp, Amblypsilopus sp, Stomoxys sp, Sarcophagidae, Dexiinae (Trichodura), Stomoxys calcitrans. We find out how many dipteran species are present in the defecations of six species of Wild and Domestic animals. In this study total of 10 flies made extensive use of animal defecates there are Stomoxys calcitrans, Neomyia sp., Muscidae, Lauxaniidae (Homoneura sp.), Stomoxys sp., Chrysomya megacephala, Bibionidae, Morellia, Musca sp., and Sarcophagidae. 15 species of blood sucking flies caught, the genus Stomoxys represented by S.Nigra and S.Calcitrans were most abundant, occurring throughout the year in large number [25]. Nectar and Cattle blood are the major food source for tabanid flies [26]. Tabanus, Chrysops, Haematopota these flies are facultative hematophagous ectoparasites, thus important from medical and veterinary point of view [27].
The flies identified in this study play an important role in the pollination of small plant species in the Nilgiris. The effect of fly pollination was significant in plants such as Tagetes erecta, Bidens pilosa, Cynoglossum zeylanicum, Justicia simplex, Nicandra physalodes, and Euphorbia helioscopia. Dipteran diversity in the Nilgiris varies from place to place but in some parts includes species harmful to human lives and animals. The Site-C Ooty Lake is a hazard to humans and animals because during the winter season, the waste water from the lake is drained and the waste soil is stagnant with the waste water. Thus Diptera is a factor in the development of certain blood-sucking insect species that are harmful to humans. Larvae of aquatic midges in the diverse water bodies of Jammu, Kashmir and Ladakh serve as food for fishes and are valuable bio-indicators of water quality [28]. In the Ooty Lake area, an important site of this study, Diptera have not been known to cause any health problems so far, as migratory birds naturally assist in controlling the high seasonal mosquitoes and blood sucking species in winter and summer. There are many medicinal plants in the valley view and hidden valley area. The family Syrphidae plays an important role in pollinating these plants. Syrphidae, Lucilia sp., and Bombyliidae pollinate most of the small flowering plants in the Nilgiris. In addition, there are some species of Diptera that feed on insects that protect them from harm by eating insects that are harmful to humans. We found a large number of species in the Hidden Valley where fly larvae are found in humid places. Keroplatidae (Orfailia fultoni, Arachnocompa spp. and Keroplatus spp.) emit a bioluminescent blue/green light as larvae. In some instances these “glow-worms” congregate in large numbers and form impressive displays [29]. Interaction with local cow breeders indicate there are no problems due to pests of This is because if the cows are exposed to any of the pests' infestations, the insects will be more likely to be found in the affected area of the cows, causing the cattle to become slightly sluggish. Stomoxys sp. and Musca sp. are found mostly in association with cattle and wild gaurs in the Nilgiris. This study suggests that these dipteran species also play an important role in climate change. Parasitize livestock and wildlife various parts of the world are transmitted by a variety of Muscid flies, including stomoxys species [30]. Although there are not many species at Site-D (Endangered Shola forest), there are more blood-sucking insects such as Haematopota sp., Amblypsilopus sp., and Stomoxys sp., due to the presence of cattle, gaur and deer. Most of the diptera insect species sit on the remains of wild and domestic cows. Cows which were left for grazing in the forest areas were the main source of blood meal for tabanid flies [31]. Orange, peach, plum, pear fruit, grapes, and guava are economically important fruits in the Nilgiris, but they are not significantly affected for yield loss by fruit flies. Genus Bactrocera are the most serious pest of guava, apricot, peach and plum [32]. Bactrocera Zonata is the predominant infesting mango fruit [33].
Funding: This study received no specific financial support. |
Competing Interests: The authors declare that they have no competing interests. |
Authors’ Contributions: Both authors contributed equally to the conception and design of the study. |
[1] T. Pape, V. Blagoderov, and M. B. Mostovski, "Order diptera linnaeus, 1758. In: Zhang, Z.-Q. (Ed.), Animal biodiversity: An outline of higher-level classification and survey of taxonomic richness," Zootaxa, vol. 3148, pp. 222-229, 2011.
[2] S. L. Clement, B. C. Hellier, L. R. Elberson, R. T. Staska, and M. A. Evans, "Flies (Diptera: Muscidae: Calliphoridae) are efficient pollinators of Allium ampeloprasum L.(Alliaceae) in field cages," Journal of Economic Entomology, vol. 100, pp. 131-135, 2007.Available at: https://doi.org/10.1093/jee/100.1.131.
[3] A. Verghese, M. Siddappaji, P. D. K. Jayanthi, and J. M. Stonehouse, "Fruit flies of economic significance in India, with special reference to Bactrocera dorsalis (Hendel). In: Barnes, B.N. (Eds.)," in Proceedings of the 6th International Symposium on Fruit Flies of Economic Importance. Stellenbosch, South Africa, 2002, p. 510.
[4] M. Kuriakose and A. Ittyachen, "An investigation into the high prevalence of hepatitis B in a rural Area of Kerala State, India: Hypothesis on Chrysops sp. (Diptera: Tabanidae) transmission," Biomed Research International, vol. 2018, pp. 1-7, 2018.Available at: https://doi.org/10.1155/2018/4612472.
[5] R. Krishnamoorthy, A. Munirathinam, K. Dhananjeyan, J. Hiriyan, T. Mariappan, P. Philip Samuel, and A. Venkatesh, "Description of a new species, toxorhynchites (Toxorhynchites) tyagii (Diptera: Culicidae), from Nilgiri hills, Western Ghats, Southern India," Zootaxa, vol. 3701, pp. 447-459, 2013.Available at: https://doi.org/10.11646/zootaxa.3701.4.4.
[6] P. Bhuyan, J. Hiriyan, P. Chandrasekaran, and C. Annadurai, "An annotated checklist of mosquito fauna with vector bionomics in Nilgiri Hills, Southern India," Journal of Evolution of Medical and Dental Sciences, vol. 2, pp. 1654-1666, 2013.Available at: https://doi.org/10.14260/jemds/440.
[7] C. Soundararajan, K. Nagarajan, and M. Arul Prakash, "Distribution of larval and pupal stages of Simulium (Diptera: Simuliidae) flies in the Nilgiris hills of Tamil Nadu," Journal of Parasitic Diseases, vol. 41, pp. 655-658, 2017.Available at: https://doi.org/10.1007/s12639-016-0861-7.
[8] R. Ravikumar, A. D. Reegan, P. Chandrasekar, and C. S. Kumar, "Distribution of dengue vectors during pre-and post-monsoon seasons in higher attitudes of nilgiri hills of Western Ghats, India," Journal of Insects, vol. 2013, pp. 1-5, 2013.Available at: https://doi.org/10.1155/2013/627304.
[9] S. Deepalakshmi and D. Jeyabalan, "Studies on mosquitocidal and biological activity of endemic plants of Nilgiris Hills against filarial vector, Culex quinquefasciatus (Say) (Insecta: Diptera: Culicidae)," International Journal of Advanced Research in Biological Sciences, vol. 4, pp. 137-151, 2017.Available at: https://doi.org/10.22192/ijarbs.2017.04.03.016.
[10] N. L. Kalra and C. Prasittisuk, "Sporadic prevalence of DF/DHF in the Nilgiri and Cardamom Hills of Western Ghats in South India: Is it a seeding from sylvatic dengue cycle – a hypothesis," Dengue Bulletin, vol. 28, pp. 44-50, 2004.
[11] H. Oldroyd, "Diptera. 1. Introduction and key to families," Handbooks for the Identification of British Insects, vol. 9, p. 49, 1954
[12] A. E. Whittington, "Manual of afrotropical Diptera. 2017. Volume 1 & 2, edited by Ashley H. Kirk-Spriggs and Bradley J. Sinclair," African Invertebrates, vol. 59, pp. 107–109, 2018.Available at: https://doi.org/10.3897/afrinvertebr.59.28076.
[13] C. E. Shannon, "A mathematical theory of communication," The Bell System Technical Journal, vol. 27, pp. 379-423, 1948.
[14] E. H. Simpson, "Measurement of diversity," Nature, vol. 163, pp. 688-688, 1949.
[15] R. Margalef, "Information theory in biology," General Systems Yearbook, vol. 3, pp. 36-71, 1958.
[16] E. C. Pielou, "Shannon's formula as a measure of specific diversity: Its use and misuse," The American Naturalist, vol. 100, pp. 463-465, 1966.Available at: https://doi.org/10.1086/282439.
[17] K. C. Sahoo, V. Sunitha, V. V. Rao, and D. S. Chary, "Diversity of diptera at agri-biodiversity Park, Hyderabad," Indian Journal of Entomology, pp. 1-4, 2021.
[18] A. H. Dhamorikar, "Flies matter: A study of the diversity of Diptera families (Insecta: Diptera) of Mumbai Metropolitan Region, Maharashtra, India, and notes on their ecological roles," Journal of Threatened Taxa, vol. 9, pp. 10865-10879, 2017.Available at: https://doi.org/10.11609/jott.2742.9.11.10865-10879.
[19] B. V. Brown, A. Borkent, P. H. Adler, D. D. S. Amorim, K. Barber, D. Bickel, S. Boucher, S. E. Brooks, J. Burger, and Z. L. Burington, "Comprehensive inventory of true flies (Diptera) at a tropical site," Communications Biology, vol. 1, pp. 1-8, 2018.
[20] A. Ssymank, C. Kearns, T. Pape, and F. C. Thompson, "Pollinating flies (Diptera): A major contribution to plant diversity and agricultural production," Biodiversity, vol. 9, pp. 86-89, 2008.Available at: https://doi.org/10.1080/14888386.2008.9712892.
[21] J. Sengupta, A. Naskar, S. Homechaudhuri, and D. Banerjee, "Diversity of hover flies (Insecta: Diptera: Syrphidae) with 3 new record from high Hill Zone of Himachal Pradesh, India," International Journal of Advancement in Life Sciences Research, vol. 2, pp. 21-37, 2019.Available at: https://doi.org/10.31632/ijalsr.2019v02i04.004.
[22] B. Mitra and P. Parui, "Diversity of true flies (Diptera: Insect A) in the Bibhutibhusan wildlife sanctuary," Records of the Zoological Survey of India, vol. 112, pp. 57-64, 2012.
[23] B. Mitra, "Diversity of flower-visiting flies (Insecta: Diptera) in India and their role in pollination," Records of the Zoological Survey of India, vol. 110, pp. 95-107, 2010.
[24] B. Mitra, S. Roy, I. Imam, and M. Ghosh, "A review of the hover flies (Syrphidae: Diptera) from India," International Journal of Fauna and Biological Studies, vol. 2, pp. 61-73, 2015.
[25] A. Ahmed, S. Okiwelu, and S. Samdi, "Species diversity, abundance and seasonal occurrence of some biting flies in Southern Kaduna, Nigeria," African Journal of Biomedical Research, vol. 8, pp. 113-118, 2005.Available at: https://doi.org/10.4314/ajbr.v8i2.35770.
[26] K. Chandra, S. Halder, A. Raha, P. Parui, and D. Banerjee, "Tabanid flies (Insecta: Diptera) from Chhattisgarh, India," Journal of Threatened Taxa, vol. 7, pp. 7720-7725, 2015.Available at: https://doi.org/10.11609/jott.o4082.7720-5.
[27] B. Narladkar and P. Shivpuje, "Fly proof net shed for livestock: A novel concept of physical barrier for integrated management of Culicoides spp.(Diptera: Ceratopogonidae)," Veterinary World, vol. 7, pp. 899-908, 2014.Available at: https://doi.org/10.14202/vetworld.2014.899-908.
[28] R. Bhagat, "Fruit fly fauna (Insecta: Diptera) of Jammu & Kashmir Himalaya, India: Check list and biodiversity," International Journal of Food, Agriculture and Veterinary Sciences, vol. 4, pp. 18-23, 2014.
[29] S. H. Jeffrey and P. Dang, "Exploring the diversity of flies (Diptera)," Biodiversity, vol. 3, pp. 3-27, 2002.Available at: https://doi.org/10.1080/14888386.2002.9712613.
[30] S. Johnson, "Stephanofilariasis-a review," in Helminthological Abstracts, Series A (Animal and Human Helminthology), 1987, pp. 287-299.
[31] R. B. Metri, G. C. Puttalakshmamma, N. L. Jaya, P. E. D’ Souza, and M. L. Satyanarayana, "Species composition, meteorological and zoogeographical aspects of the horsefly fauna (Diptera: Tabanidae) in the Western Ghats, Karnataka, India," International Journal of Current Microbiology and Applied Sciences, vol. 9, pp. 2636-2649, 2020.Available at: https://doi.org/10.20546/ijcmas.2020.907.310.
[32] J. M. Stonehouse, J. D. Mumford, and G. Mustafa, "Economic losses to tephritid fruit flies (Diptera: Tephritidae) in Pakistan," Crop Protection, vol. 17, pp. 159-164, 1998.Available at: https://doi.org/10.1016/s0261-2194(97)00091-4.
[33] J. S. Choudhary, B. Das, S. Maurya, and S. Kumar, "Diversity and population dynamic of fruit flies species in methyl eugenol based parapheromone traps in Jharkhand region of India," 2012.
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