Translator Disclaimer
1 October 2013 Altitudinal and Seasonal Variation in Drosophila Species on Mount Japfu of Nagaland, a Sub-Himalayan Hilly State of India
Bovito Achumi, Shridhar N. Hegde, Pardeshi Lal, Sarat Chandra Yenisetti
Author Affiliations +
Abstract

Drosophila (L.) (Diptera: Drosophilidae) has richly contributed to the understanding of patterns of inheritance, variation, speciation, and evolution. Drosophila, with its cosmopolitan nature and complexities in species compositions, is an excellent model for studying the eco-distributional patterns of various species. This study analyzed the altitudinal and seasonal variation in Drosophila species of Mount Japfu in Nagaland, a sub-Himalayan hilly state of northeast India, over the course of one year. A total of 4,680 Drosophila flies belonging to 19 species of 4 subgenera were collected at altitudes of 1500, 1800, 2100, 2400, and 2700 m a.s.l. The subgenus Sophophora Sturtevant was predominant, with 10 species, followed by subgenus Drosophila, with 4 species. Subgenus Dorsilopha and subgenus Scaptodrosophila were represented by 1 species each. The remaining 3 species were not identified. Cluster analysis and constancy methods were used to analyze the species occurrence qualitatively. Altitudinal changes in the population densities and relative abundances of the different species at different seasons were also studied. The diversity of the Drosophila community was assessed by applying Simpson's diversity index. At 1800 m a.s.l., the Simpson's index was low (0.09301), suggesting high Drosophila diversity at this altitude. The density of Drosophila changed significantly during different seasons (F = 26.72; df = 2; p < 0.0001). The results suggest the distributional pattern of a species or related group of species was uneven in space and time.

Introduction

The fruit fly Drosophila (L.) (Diptera: Drosophilidae) has richly contributed to the understanding of patterns of inheritance, variation, speciation, and evolution. Genus Drosophila, with its cosmopolitan nature and complexities in species compositions, is an excellent model for studying the ecodistributional patterns of various species (Carson 1965). Systematic study concerning the variations in the species compositions and the patterns of distribution of various members of the genus Drosophila in different geographical regions of the world will enable understanding of the principles underlying adaptive radiation and certain mechanisms involved in speciation (Muniyappa 1981).

Significant progress has been made in the fields of taxonomy and systematics of the family Drosophilidae in India. This family is composed of more than 3,500 species throughout the world (Bachli 1998). About 200 species belonging to 20 genera have been reported from different parts of India. However, very little is known regarding the Drosophila fauna of the northeastern region of the Indian subcontinent. This region is one of the richest repositories of biodiversity in the world, with its diverse climatic conditions, variable altitudes, deep valleys, luxuriant flora, running streams and moist surroundings. So, it provides an ideal location for the colonization of several Drosophila species (Singh and Gupta 1977; Dwivedi and Gupta 1979; Gupta and Singh 1979; Singh and Gupta 1980; Singh 1987). This region includes eight hill states, namely Assam, Arunachal Paradesh, Manipur, Meghalaya, Mizoram, Nagaland, Sikkim, and Tripura. A preliminary survey on Drosophilids of Dimapur, Medziphema, and Kohima of Nagaland state was conducted (Singh 1987). A preliminary report was published by Yenisetti et al. (2002) on Drosophilids of Mokokchung town. However, no systematic comprehensive study has been done on Drosophilids of Nagaland, a sub-Himalayan hilly state in the northeast region of India. It is possible that new Drosophila species can be identified from this region. Drosophila is a pollinator for economically important plants, such as Ceropegia (Chaturvedi 2006). It is possible that novel Drosophila pollinators for other economically important plants can be identified in these subtropical rain forests.

The ecological and biological diversity of an ecosystem determines the presence or absence of a species in an ecological niche. Apart from physical and biotic factors, the topography and season also affect animal distribution. As elevation is one of the important aspects of topography, it is important to look at animal distribution from that perspective. Efforts have been made to collect Drosophila from different altitudes, but these data were not considered with an ecological perspective (Reddy and Krishnamurthy 1977). According to Reddy and Krishnamurthy (1977), physical and biotic factors are the sole determinants of animal distribution. This idea logically denotes that elevation and season have no influence on animal distribution. In the present study, our goal was to determine if elevation affects distribution.

According to Gause's competitive exclusion theory, two related species competing for the same resources cannot co-exist together in the same ecological niche (Gause 1934). However, laboratory experiments questioned the validity of this principle (Ayala 1969). The presence of taxonomically or phylogenetically related species in an ecological niche indicates their coexistence, and absence of such related species infers competitive exclusion (Guruprasad et al. 2010). Our study sought to understand whether taxonomically or phylogenitically related Drosophila species coexist in nature. Our study also has been undertaken to understand the altitudinal and seasonal variation of Drosophila species on Mount Japfu, which is situated 15 km from Kohima, the capital of the sub-Himalayan hilly state Nagaland, India.

Materials and Methods

The altitudinal and seasonal fluctuation in Drosophila fauna was studied in five different wild localities of Mount Japfu, which has a peak altitude of about 3015.60 m a.s.l. Its slopes are covered with thick vegetation. The selected collection spots were located at 25° 11′ N latitude and 94° 55′ E longitude. Monthly collections of flies were made at the altitudes of 1500, 1800, 2100, 2400, and 2700 m a.s.l. from April 2010 to March 2011. Both bottle trapping and net sweeping methods were used. For bottle trapping, milk bottles of 200 mL capacity containing a smashed ripe banana sprayed with yeast were tied to the twigs underneath small bushes at the height of 1–1.5 m above the ground. Fifteen traps were kept at each site. After 2 days, the mouth of each bottle was plugged with cotton and removed from the bushes. The flies that were attracted by the bait and collected in the bottles were transferred to fresh bottles containing wheat cream agar medium. The medium was prepared by adding 100 g of sugar (jaggery) to 500 mL of water and boiling it. Then, 500 mL of water, 100 g of wheat powder (soji), and 8 g of agar-agar were added to the boiling sugar water mixture. When the medium turned sticky, 7.5 mL propionic acid (anti-fungal agent) was added while continuously stirring the medium.

Net sweeping was done on rotting fruits (crushed banana spread beneath shaded areas of bushes 1 day before collection). After each sweep, collected flies were transferred to bottles containing freshly prepared wheat cream agar medium.

The flies were then brought to the laboratory, isolated, identified, and sexed. Categorization of the collected Drosophila flies was made to respective taxonomic groups by employing the parameters as suggested by Sturtevant (1921), Patterson and Stone (1952), Throckmorton (1962), and Bock (1971). To study seasonal variation, the entire year was divided into three seasons: pre-monsoon, extending from January through March, monsoon, from April through September, and post-monsoon, from October through December.

Flora of the collection sites:

Following is a brief description of the flora available in each of the collection spots.

Flora at 1500 m a.s.l.: maibau, Alnus nepalensis (Don) (Fagales: Betulaceae); beggarticks, Bidens spp (Asterales: Asteraceae); bittervine, Makania spp; sow thistles, Sonchus spp; butterfly bush, Buddleja spp (Lamiales: Scrophulariaceae); brahmi booti, Centella asiatica (L.) (Apiales: Apiaceae); sirib large, Entada pursathea (Roux) (Fabales: Fabaceae); banana, Musa spp (Zingiberales: Musacae); carrion flowers, Smilax spp (Liliales: Smilacaceae); pinyin, Stemona spp (Pandanales: Stemonaceae); currant tomato, Solanum spp (Solanales: Solanaceae); marda, Termenalia elliptice (Wright & Arn) (Myrtales: Combretaceae); etc.

Flora at 1800 m a.s.l.: jackfruit, Artocarpus hetrophyllus (Lam) (Rosales: Moraceae); yellow Himalayan raspberry, Rubus spp (Rosaceae); wormwood, Artemisisia vulgaris (L.) (Asterales: Asteraceae); beggar-ticks, Bidens spp; bamboo, Bambusa spp, (Poales: Poaceae); black musale, Curculigo spp (Asparagales: Hypoxidaceae); timburni, Diospynum spp, (Ericales: Ebenaceae); deereye beans, Mucuna perita (Adans) (Fabales: Fabaceae); tapioca-root, Maninot utilissema (Crantz) (Malpighiales: Euphorbiaceae); Smilax spp; khasi pine, Pinus insularies (Gordon) (Pinales: Pinaceae); knotwood, Polygonum spp (Caryophyllales: Polygonaceae); etc. Flora at 2100 m a.s.l.: A. nepalensis (Don); khang, Acacia pinnata (Miler) (Fabales: Fabaceae); thickhead, Crossocephalum spp (Asterales: Asteraceae); Himalayan nettle, Girardinia heterophylla (Vahl) (Rosales: Urticaceae); Rubus spp; blady grass, Imperata cylindrica (Brauv) (Poales: Poaceae); Musa spp; etc.

Flora at 2400 m a.s.l.: bologi, Crossocephalum spp (Asterales: Asteraceae); A. vulgaris; white weed, Ageratum conyzoids (L.); thoroughworts, Eupatorium spp; Bidens spp; blueberry ash, Elaeocarpus spp (Oxalidales: Elaeocarpaceae); shaking brake, Pteris spp (Polypodiales: Pteridaceae); I. cylindrica; C. asiatica; P. insularies; knotwood, Polygonum spp; cowitch, Mucuna pruriens (L.) (Fabales: Fabaceae); etc.

Flora at 2700 m a.s.l.: Crossocephalum spp; Curculigo spp; I. cylindrica; kamraj, Helminthostachys zeylanica (L.) (Ophioglossales: Ophioglossaceae); Polygonum spp; Smilax spp; timburni, Dryopteris spp (Ericales: Ebenaceae); rhododendron, Rhododendron spp (Ericaceae); etc.

Data analysis

The relationship between the abundance, richness, and diversity of all groups of flies collected throughout the year was calculated by Simpson's diversity index (Simpson 1949). Simpson's diversity index (D) measures the probability that 2 individuals randomly selected from a sample will belong to the same species, and was calculated using the following formula:

Where n = the total number of organisms of a particular species, and N = the total number of fi01_01.gif organisms of all populations.

In order to verify the qualitative distribution of different species, the occurrence constancy method (Dijoz 1983) was used. The constancy value (C) was obtained by dividing the number of collections in which one species occurred by the total number of collections, and then multiplying that result by 100. Based on constancy value, the species collected were grouped as constants when C ≥ 50, accessory species when C ≥ 25 and < 50, and accidental species when C < 25. Species that occurred in only one area were considered exclusive.

To understand the difference in seasonal variation of Drosophila flies at Mount Japfu, oneway analysis of variance was performed using GraphPad Prism5 software ( www.graphpad.com).

Cluster analysis was performed using WinSTAT software ( www.winstat.com) to design, analyze, and compare different Drosophila populations, as described by Giri et al. (2007). In the cluster study, Euclidean distance was chosen to measure the similarity between different species, and Ward's strategy (Giri et al. 2007) was performed to unite two clusters.

Table 1.

The list of species of Drosophila collected, and the number of Drosophila collected at different altitudes (m a.s.l.) of Mount Japfu from April 2010 to March 2011.

t01_01.gif

Results

The list of Drosophila species collected at different altitudes of Mount Japfu from April 2010 through March 2011 and their taxonomic position are given in Table 1. A total of 19 species were collected, including 16 species of Drosophila belonging to 4 subgenera (Sophophora, Drosophila, Dorsilopha and Scaptodrosophila). The remaining 3 species were not identified. Pooled data on monthly collections of Drosophila yielded a total of 4680 individuals. Out of these, 2889 individuals (61.73%) belonged to 10 species of subgenus Sophophora, 1578 (33.71%) individuals belonged to 4 species of the subgenus Drosophila 100 (2.13%), 3 were unidentified, 62 (1.32%) individuals belonged to 1 species of subgenus Scaptodrosophila, and 51 (1.07%) belonged to 1 species of subgenus Dorsilopha.

The value of the Simpson's index, indicating the abundance, richness, and diversity of Drosophila flies at different altitudes, is given in (Table 3). At the lowest altitude (1500 m a.s.l.), the Simpson's index was 0.10903, and at the highest altitude (2700 m) it was 0.141355.

The altitudinal variation of the Drosophila population is depicted in (Figure 1). The number of Drosophila flies decreased with increasing altitude. The altitudinal variations of the most abundant Drosophila species are shown in (Figure 2).

The seasonal variation in the population density of Drosophila is depicted in Figure 3. The density was low in the pre-monsoon period, increased in the monsoon period, and then decreased in the post-monsoon period. The analysis of variance calculated for premonsoon, monsoon, and post-monsoon seasons showed significant differences among them (F = 26.72; df = 2, p < 0.0001).

Table 2.

Absolute (A) and relative abundance (r) and constancy values (c) for each species collected at different altitudes of Mount Japfu from April 2010 to March 2011.

t02_01.gif

Table 3.

Simpson's diversity index (D) according to the altitude of Mount Japfu.

t03_01.gif

The constancy value (C) of all species at all altitudes along with absolute numbers and relative abundance are presented in Table 2. Constant species (C ≥ 50) represented 36.84% of the total collected species (7 out of 19), while 8 species were considered accessory (42.10%), and 4 species were considered accidental (21.05%). Constant species were Drosophila bipectinata (Duda) (Diptera: Drosophilidae), D. eugracilis (Bock and Wheeler), D. kikkawai (Burla), D. malerkotliana (Parshad and Paika), D. takahashii (Sturtevant), D. immigrans and D. paraimmigrans; accessory species were D. jambulina (Parshad and Paika), D. parvula (Bock and Wheeler), D. rajasekari (Reddy and Krishnamurthy), D. trileuta (Bock and Wheeler), D. nasuta (Lamb), D. replete (Wollaston), D. buskii (Coquilett), and unidentified species (1); accidental species were D. agumbensis (Prakash and Reddy), D. nigra (Grimshaw), unidentified (2) and unidentified (3). In the cluster analysis (Figure 4), the accidental species stand first in the cluster, followed by the accessory species, and the bottom is occupied by constant species. D. agumbenesis, D. jambulina, D .rajasekari, D. trileuta belong to melanogaster species group of the subgenus Sophophora. D. nigra belongs to subgenus Scaptodrosophila. D. agumbenesis and D. jambulina belong to montium subgroup and D. bipectinata belongs to the ananassae subgroup. D. repleta, D. buskii of the same cluster belongs to subgenus Drosophila. In the second cluster D. eugracilis, D. kikkawai and D. parvula belong to the melanogaster species group of the subgenus Sophophora and D. paraimmigrans, D. immigrans of the same cluster belong to subgenus Drosophila. D. takahashii belongs to melanogaster species group of subgenus Sophophora.

Discussion

The density of Drosophila on Mount Japfu decreased with increasing altitude. The density was high at 1500 and1800 m a.s.l., but was low at 2700 m a.s.l. (Figure 1). The results indicate that the Drosophila community was affected by elevation. Wakahama (1961, 1962) has reported similar altitudinal variation in the distribution of Drosophila on Mt. Dakesan in Japan. He noticed that the total density of all species decreased with increasing altitude. Reddy and Krishnamurthy (1977) also noticed such altitudinal variation in Drosophila populations in the Jogimatii hills of Karnataka. Guruprasad et al. (2010) also observed seasonal and altitudinal variation in Drosophila populations of Chamundi Hill in Mysore, Karnataka, India. The reasons behind the observed phenomenon can be attributed to changes that occur as one ascends an altitudinal transect, potentially involving changes in temperature, precipitation, partial pressure of atmospheric gases, atmospheric turbulence and wind speed, and radiation input, including short-wave ultra-violet radiation at different wavelengths (Barry 1992). According to Hodkinson (2005), the above-mentioned changes are often strongly interactive and together create an environmental envelope within which insect species survive and reproduce. Hodkinson (2005) further emphasizes that the abovementioned parameters combine to produce a general decrease in the overall structural complexity of the insects' habitat with increasing altitude.

According to Hegde et al. (2000a), the growth and size of a population depends on several environmental factors in addition to genetic structure. In the present study, consideration of the common and abundant species shows that numerical variation exists in regard to these species at all five altitudes. The occurrence of the dominance of one species over the others in any given area can be correlated with the dominant species' ecological versatility to exploit the conditions available in those habitats. The present study corroborates with the work of Muniyappa and Reddy (1981), Hegde et al. (2001), and Vasudev et al. (2001). There may be many other unknown microclimatic conditions that could also affect the density of Drosophila. The results of our study are in concurrence with the work of Cooper and Dobzhansky (1956), Reddy and Krishnamurthy (1977), Hegde et al. (2001), all of which have shown the influence of microclimatic conditions on the diversity of Drosophila. The present findings are also in agreement with the work of Cooper and Dobzhansky (1956) on species of Drosophila inhabiting the Sierra Nevada Mountains of the Yosemite region of California, where some of the species occurred at all elevations at which collections were made (259-3353 m a.s.l.). The results of our study are also in agreement with the work of Guruprasad et al. (2010), who showed that the number and density of Drosophila species decreased with increasing altitude at Chamundi Hill in Mysore, Karnataka. In our study, the presence of more species at lower altitudes can be attributed to the existence of thick vegetation, which provided good sources of food, and a more congenial environment at lower altitudes than at the higher altitudes.

Significant variations in the density of Drosophila were noticed during different seasons of the year on Mount Japfu. The density was highest during monsoon season at all altitudes and lowest during the pre-monsoon season. Possible reasons for the high density during monsoon season could be the availability of adequate food in the form of rotting fruits and the congenial climate for multiplication of the flies. The fact that the fruiting season of many plants in the area coincides with the monsoon season offers support for this conclusion. The monsoon season is characterized by heavy rains, reductions in temperature, and increases in humidity. As the monsoon season recedes, rainfall and humidity decrease, leading to a dry climate. The population density also starts declining in post-monsoon season, reaching its minimum during the pre-monsoon season. Thus, the fluctuations in population size of Drosophila could be closely related to the wet and dry seasons. However, in temperate regions, the population density declines to an extremely low level during cold winter months, indicating the influence of temperature on the regulation of population size, as is the case in several Drosophila species inhabiting temperate regions (Dobzhansky 1943; Patterson and Wagur 1943; Dobzhansky and Pavan 1950; Williams and Miller 1952; Wakahama 1961).

According to the constant, accessory, and accident species, as well as the cluster analysis, our study indicates several species that coexisted had similar ecological preferences.

In Simpson's diversity index (D), 0 represents infinite diversity, and 1 represents no diversity, i.e., the greater the value of D, the lower the diversity. Applying this index to understand the measures of biodiversity of flies at different altitudes of Mount Japfu shows that the second lowest altitude studied (1800 m a.s.l.) had the lowest D-value, indicating more biodiversity compared to other altitudes. Hodkinson (2005) suggested that the altitudinal distribution of an insect species is controlled by its environmental tolerances, with maximum population size being achieved at some optimum elevation and population density declining with altitude above and below the optimum. The results of our study suggest that the optimum elevation on Mount Japfu for Drosophila diversity is at 1800 m a.s.l. From the eco-distributional analysis of Drosophila species on Mount Japfu, it is clear that the distributional pattern of a species or related group of species is uneven in space and time. The Drosophila community of Mount Japfu was highly diverse and depended on several environmental factors in addition to the genetic structure of the species present in it.

Figure 1.

Altitudinal variation in the population of Drosophila species on Mount Japfu. High quality figures are available online.

f01_01.jpg

Figure 2.

Altitudinal variation in the population of the most abundant Drosophila species on Mount Japfu. High quality figures are available online.

f02_01.jpg

Figure 3.

Seasonal variation in Drosophila flies collected from Mount Japfu (F = 26.72; df = 2; p < 0.0001). High quality figures are available online.

f03_01.jpg

Figure 4.

The cluster analysis of Drosophila species found on Mount Japfu (dendrogram using Ward's method). High quality figures are available online

f04_01.jpg

Acknowledgements

We thank the Department of Zoology Nagaland University, and the Chairman of the Department of Studies in Zoology, Manasagangatori, Mysore, India, for facilities. We also thank the University Grants Commission, New Delhi, for financial support.

References

1.

FJ Ayala . 1969. Experimental invalidation of the principle of competitive exclusion. Nature 224: 1076–1079. Google Scholar

2.

G Bachli . 1998. Family Drosophilidae. In: L Papp , B Darvas , Editors. Contributions to a manual of palearctic Diptera. III. Higher Brachteera. Science Herald. Google Scholar

3.

RG Barry . 1992. Mountain climatology and past and potential future climatic changes in mountain regions. Mountain Research and Development. 12: 71–86. Google Scholar

4.

IR Bock . 1971. Taxonomy of the Drosophila bipectinata species complex. University of Texas Publication 6: 273–280. Google Scholar

5.

HL Carson . 1965. Chromosomal polymorphism in geographically wide spread species of Drosophila. In: HG Baker , GL Stebblins , Editors. Genetics of Colonizing Species. pp. 503–531. Academic Press. Google Scholar

6.

DM Cooper , TH Dobzhansky . 1956. Studies on the ecology of Drosophila in the Yosemite region of California. 1. The occurrence of species of Drosophila in different life zones and at different seasons. Ecology 37: 526–533. Google Scholar

7.

SK Chaturvedi . 2006. Indian Ceropegias and their pollination biology. In: S Kumar , Editor. Plant Science Research in India: Challenges and Prosepects. Botanical Survey of India, Dehradun. Google Scholar

8.

TH Dobzhansky . 1943. Genetics of natural populations IX. Temporal changes in the composition of population of Drosophila pseudoabscura. Genetics 28: 168–186. Google Scholar

9.

TH Dobzhansky , C Pavan . 1950. Local and seasonal variations in relative frequencies of species of Drosophila. Brazilian Journal of Animal Ecology 19: 1–14. Google Scholar

10.

YN Dwivedi , JP Gupta . 1979. Three new Drosophilids (Diptera; Drosophilidae) from northeast India. Entomon 4(2): 183–187. Google Scholar

11.

R Dijoz . 1983. Ecologia Geral. Editora Vozes Petropolis. Google Scholar

12.

GF Gause . 1934. The struggle for existence. Williams and Wilkins. Google Scholar

13.

D Giri , VK Murthy , PR Adhikary , SN Khonal . 2007. Cluster analysis applied to atmosphere PM10 concentration data for determination of sources and spatial patterns in ambient air quality of Kathmandu valley. Current Science 93(5): 684–688. Google Scholar

14.

JP Gupta , BK Singh . 1979. Two new species of Drosophila (Diptera: Drosophilidae) from Shillong, Meghalaya. Entomon 4(2): 167–172. Google Scholar

15.

BR Guruprasad , SN Hegde , MS Krishna . 2010. Seasonal and altitudinal changes in population density of 20 species of Drosophila in Chamundi hill. Journal of Insect Science 10:123. Available online:  http://www.insectscience.org/10.123  Google Scholar

16.

SN Hegde , MK Naseerulla , MS Krishna . 2000. Variability of morphological traits in Drosophila bipectinata complex. Indian Journal of Experimental Biology 38: 797–806 Google Scholar

17.

SN Hegde , V Vasudev , MS Krishna . 2001. Biodiversity of Drosophila of South India. In: BB Hosetti , M Venkateshwarulu , Editors. Wildlife Biodiversity Conservation Management, Volume 1. pp. 55–71. Daya Publishing House. Google Scholar

18.

ID Hodkinson . 2005. Terrestrial insects along elevation gradients: species and community response to altitude. Biological Reviews 80: 489–513. Google Scholar

19.

N Muniyappa . 1981. Cytotaxonomy and population genetics of Drosophila of Coorg (Western Ghats) Karnataka. Ph.D. Thesis. University of Mysore, Mysore, India. Google Scholar

20.

N Muniyappa , GS Reddy . 1981. Description of a new species, Drosophila gangotrii (Diptera: Drosophilidae) from South India. Bombay Journal of Natural History Society 77(3): 486–490. Google Scholar

21.

JT Patterson , RP Wagur . 1943. Geographical distribution of species of the genus Drosophila in the United States and Mexico. University of Texas Publication 4313: 217–281. Google Scholar

22.

JT Patterson , WS Stone . 1952. Evolution in the genus Drosophila. Macmillan Company. Google Scholar

23.

GS Reddy , NB Krishnamurthy . 1977. Distribution of different species of Drosophila in Jogimatti hills, Chitradurga district, Karnataka, India. Drosophila Information Service 52: 105. Google Scholar

24.

EH Simpson . 1949. Measurement of diversity. Nature 163: 688–688. Google Scholar

25.

BK Singh , JP Gupta . 1977. Two new and two unrecorded species of the genus Drosophila (Diptera: Drosophilidae) from Shillong, Meghalaya. India. Proceedings of Zoological Society of Calcutta 30: 31–38. Google Scholar

26.

OP Singh , JP Gupta . 1980. Description of three new species of Drosophila (Drosophilidae) from northeast India. Oriental Insects 14(4): 503–509. Google Scholar

27.

OP Singh . 1987. Drosophilidae in North Eastern India: A preliminary survey in Nagaland. Drosophila Information Service 66: 67. Google Scholar

28.

AH Sturtevant . 1921. The North American Species of Drosophila. Carnegie Institution of Washington Publication 301: 1–141. Google Scholar

29.

LH Throckmorton . 1962. The problem of phylogeny in the genus Drosophila. University Texas Publication 6205: 207–345. Google Scholar

30.

V Vasudev , HJ Nagaraj , Nagabhushana, SN Hegde . 2001. Altitudinal and seasonal distribution of Drosophila species in North Kanara region of Western Ghats. Entomon 26 (special issue): 326–331. Google Scholar

31.

DD Williams , DD Miller . 1952. A report on Drosophila collection in Nebraska. Bulletin of the University of Nebraska State Museum 3: 1–19. Google Scholar

32.

KL Wakahama . 1961. Notes on the seasonal activity of Drosophila observed. In: M Ashburner , HL Carson , JN Thompson Jr., Editors. Genetics and Biology of Drosophila. pp. 1–97. Academic Press. Google Scholar

33.

KL Wakahama . 1962. Studies on the seasonal variation of population structure in Drosophila, I. Seasonal activity of Drosophilid flies observed on Mt. Dakesan. Annotationes Zoologicae Japonenses 35: 234–242. Google Scholar

34.

SC Yenisetti , SN Hedge , MS Krishna . 2002. A preliminary report on Drosophilids of Mokokchung (Nagaland State, India). Drosophila Information Service 85: 16–17. Google Scholar
This is an open access paper. We use the Creative Commons Attribution 3.0 license that permits unrestricted use, provided that the paper is properly attributed.
Bovito Achumi, Shridhar N. Hegde, Pardeshi Lal, and Sarat Chandra Yenisetti "Altitudinal and Seasonal Variation in Drosophila Species on Mount Japfu of Nagaland, a Sub-Himalayan Hilly State of India," Journal of Insect Science 13(117), 1-12, (1 October 2013). https://doi.org/10.1673/031.013.11701
Received: 30 March 2012; Accepted: 6 June 2013; Published: 1 October 2013
JOUR