Food preferences of the Golden Jackal Canis aureus in the Gir National Park and Sanctuary, Gujarat, India


M. Shamshad Alam 1, Jamal A. Khan 2, Chege H. Njoroge 3, Sandeep Kumar 4 & R.L. Meena 5


1,2 Department of Wildlife Sciences, Aligarh Muslim University, Aligarh, Uttar Pradesh 202002, India

1 Present address: Regional Planner, BCRLI Project, Gir Learning Centre, Wildlife Division, Sasan-Gir, Junagadh, Gujarat 362135, India

3 Kenya Wetland Biodiversity Research Team, National Museums of Kenya, Nairobi, Kenya

4 DCF, Wildlife Division, Gujarat Forest Department, Sasan-Gir, Junagadh, Gujarat 362135, India

5 CCF, Wildlife Circle, Gujarat Forest Department, Sardarbaug, Junagadh, Gujarat 362001, India

1 (corresponding author), 2, 3, 4, 5



Abstract: The feeding habits of the Golden Jackal Canis aureus were investigated by analysis of its scat contents (n=81), collected between October 2007 and June 2008 in Gir National Park and Sanctuary, Gujarat, India. Jackal dietary habits reflected the availability of a wide variety of food items and the differential vulnerability of prey. Potential animal and plant foods available to jackal varied because of their seasonal variability. About 32.69% scats were found to have only one prey item, whereas 48.08% of scats represented two prey items. Overall, it was found that the large mammalian prey was the most important food item which was significantly supplemented by vegetative material particularly Zizyphus spp. Amongst mammalian prey, the percentage frequency of occurrence (percentage±SE) of Chital Axis axis was 25.93±2.84, Buffalo Bubalus arnee bubalis was 27.16±2.98 followed by Indian Hare Rufus nigricollis 19.75±2.15 and Sambar Rusa unicolor 11.11±1.19 while the least was found for Langur Semnopithecus entellus 2.47±0.21 and Bluebull Boselaphus tragocamelus 2.47±0.21. Although, there is substantial availability of wild prey kills, the results suggest the presence of domestic mammals and human waste matter in the scats which could be assumed as a fortification of the Jackal’s dietary spectrum, substantiating the scavenging tendency of the jackal to forage near human settlements.


Keywords: Canis aureus, food habit, Golden Jackal, Gir National Park and Sanctuary, scat analysis.






Editor: Mewa Singh, University of Mysore, Mysuru, India. Date of publication: 26 February 2015 (online & print)


Manuscript details: Ms # o3954 | Received 20 February 2014 | Final received 15 January 2015 | Finally accepted 30 January 2015


Citation: Alam, M.S., J.A. Khan, C.H. Njoroge, S. Kumar & R.L. Meena (2015). Food Preferences of the Golden Jackal Canis aureus in the Gir National Park and Sanctuary, Gujarat, India. Journal of Threatened Taxa 7(2): 6927–6933;


Copyright: © Alam et al. 2015. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use of this article in any medium, reproduction and distribution by providing adequate credit to the authors and the source of publication.


Funding: Financial support was provided by Ministry of Environment & Forest (Government of India) under Gir Hyena Ecology Project. Department of Wildlife Sciences, Aligarh Muslim University, Aligarh and Gujarat Forest Department provided institutional and logistic support, respectively.


Competing Interest: The authors declare no competing interests.


Acknowledgements: We are thankful to Ministry of Environment & Forest, Government of India for financial support, and Gujarat State Forest Department for permission to carry out the study in GNPS. We are thankful to the Department of Wildlife Sciences, Aligarh Muslim University for logistic and institutional support. We are very much thankful to three anonymous reviewers for their valuable comments and suggestions helped in improving the quality of this paper. We are also thankful to field assistants Dost Mohammad Bloch and Sabdad Bloch for help in field work.





The Golden Jackal Canis aureus, a medium-sized predator and omnivore, is one of the most widely distributed canid species, occurring in many areas of central, eastern, and southern Europe, northern Africa, and parts of Asia with a range extending from the Arabian Peninsula into western Europe and east into Turkey, the Middle East, Central Asia, the entire Indian subcontinent south to Sri Lanka, and east to Myanmar, Thailand, and parts of Indo-China (Prater 1980; Sillero-Zubiri et al. 2004; Jhala & Moehlman 2008; Katuwal & Dahal 2013). During the past about half century, its populations in many parts of its geographical range have undergone significant changes in distribution and abundance, including drastic declines (Jhala & Moehlman 2008). Over most of its distribution, the jackal is fairly common, although it is thought to be declining in many areas due to poaching, habitat loss and modification. In south-eastern Europe, the preferred habitat of the jackal consists of a mosaic of small cultivations and dense scrub as well as lowland or wetlands with adequate vegetation covers (Macdonald 1984; Giannatos 2004; Katuwal & Dahal 2013). With increasing anthropogenic pressures it is facing threats and has started disappearing from many places of its global distribution range. The causes of decline seem to be related to the limited habitat availability due to changes in human agro-pastoral activities, which resulted mainly in reduced day-cover availability and possibly reduced food base as well. Other than forest areas of different habitats and mountainous areas, agricultural habitats are also being occupied by jackal in high numbers (Russev 2010). The species is included in the Convention on International Trade in Endangered Species (CITES) Appendix III, listed as a species of ‘Least Concern’ as per the International Union for Conservation of Nature (IUCN) Red List of Threatened Species. It is a schedule III species in The Wildlife (Protection) Act, 1972 of India, receiving legal protection (Jhala & Moehlman 2008).

The jackal is an opportunistic canid species, showing high flexibility in hunting strategies according to actual food availability (Lamprecht 1978; Macdonald 1983; Demeter & Spassov 1993). Its diet pattern varies across a wide distribution whereas its food spectrum ranges from plants, arthropods and reptiles to birds, lagomorphs and rodents; it also preys upon young domestic or wild ungulates, and is also considered a scavenger (Demeter & Spassov 1993; Yom-Tov et al. 1995; Jhala & Moehlman 2008). It is a very valuable animal in the tropical ecosystem; acting in many ways in balancing the eco-cycles and keeping the environment clean (Prater 1980). In India, it is widely distributed and also marks its presence in many protected areas, but the information available on this species is scanty.

The Gir National Park and Sanctuary (GNPS) is one such protected area which supports a very high density of large predators including the Asiatic Lion Panthera leo persica and the Common Leopard Panthera pardus along with a healthy population of herbivores and livestock (Khan et al. 1996; Singh & Kamboj 1996; Singh & Gibson 2011; Meena & Kumar 2012). We assumed that large carnivores provide ample opportunity to jackal to feed in terms of providing kills and thus, supporting this species, even in the presence of a large scavenger/competitor in the form of Striped Hyena Hyena hyena (Alam 2011; Alam et al. 2014). Therefore, we investigated the feeding habits of jackal by analysing faecal scat samples. Since, no quantitative information is available on the food spectrum and feeding habits of this species in the Gir ecosystem, this study presents the first ever record of jackal feeding habits in a typical dry-deciduous forest area of the GNPS.


Materials and Methods

Study Area

The study was carried out in the GNPS, located in the Gujarat province of India (Fig. 1). GNPS (20040’21050’N & 70050’71015’E) lies around 40km away from the Arabian Sea coast in the Kathiawar or Saurashtra peninsula of Gujarat State. It stretches over a length of about 70km from west to east and about 40km from north to south. The maximum and the minimum temperature is 450C in summer and 70C in winter. The rainfall pattern is erratic and uneven, with the maximum and minimum annual rainfall being 1866mm and 199mm, respectively averaging to 980mm. There are 45 small temporary settlements of Maldhari graziers locally known as Ness.






GNPS is well known for the only wild population of the Asiatic Lion. The total area of GNPS is 1412.13km² of which the National Park comprises 258.71km² surrounded by 1153.41km² of sanctuary. It also supports a rich biodiversity, viz.: 606 recorded flowering plant species, 39 mammal species, 37 reptiles, 300 species of birds and more than 2000 species of insects (Alam 2010, 2011; Meena & Kumar 2012). According to Champion & Seth (1968), the GNPS falls under the type 5A/Cla, i.e., very dry teak forest. The area comprises low hills of volcanic origin with an altitudinal range of 83524 m.



It is difficult to determine each prey item contributing to the diet of a carnivore species by direct observations in the field. Scat analysis is, thus widely used for studying food habits of carnivores because of its non-invasive nature and easy collection and analysis (Korschgen 1980; Ackerman et al. 1984). Therefore the scat analysis method was used to determine the food habits of jackals in the GNPS.

Jackal scats are very easy to identify in the field (Majumder et al. 2011) and we found no ambiguity and confusion in differentiating jackal scats from that of the Indian Fox Vulpes bengalensis which is generally found in the fringe areas of the sanctuary. Scats were collected near identified active dens of jackals and stored in zipped polythene bags with ancillary information like place, habitat, GPS coordinates and date of the collection. The scats were collected between October 2007 and June 2008 in GNPS. Each scat was crushed very carefully avoiding any mix-up and indigestible prey remains such as hairs, bones, claws, hooves, teeth, feathers and other materials were used for identification of prey species (Lockic 1959; Korschgen 1980; Mukherjee et al. 1994; Jethva & Jhala 2003). The hairs were the most important factor used to determine the prey species in the scats. Hairs were collected randomly from each scat and treated with xylol and subsequently with xylene. From each scat, 20 hairs were taken randomly for microscopic examination using a compound stereoscopic microscope (Olympus CH 20i) under 40X magnification. The microscopic examination of hairs and their characteristics such as medullary and cuticular patterns were observed and compared with reference slides. The reference slides of all possible prey species found in the study area were prepared. The reference slides of hair samples were collected from the field as well as from Sakkarbag Zoo.

The percentage occurrence of a mammalian prey item was calculated as the number of times a specific prey item was found to occur in scat and expressed as a percentage of all prey occurrences (Floyed et al. 1978; Weaver & Fritts 1979; Ackerman et al. 1984). The frequency of occurrence of prey species in the scats was computed as the number of occurrence of each prey type divided by the total number of scat analyzed and expressed as a percentage (Leoplod & Karusman 1986; Corbett 1989; Reynold & Aebischer 1991; Jethva & Jhala 2004). The standard error (SE) was estimated from the percentage occurrence of each mammalian prey species and 95% confidence interval was obtained by multiplying the SE by 1.96 (Fowler et al. 2006). Diet content other than mammalian prey was also calculated as the number of times a specific item was found to occur in scat and expressed as a percentage of occurrences of all items other than mammalian prey. Data was visualized as bar plots using the statistical program R (R Development Core Team 2008).



Table 1 shows the occurrence of the number of prey items in the scat of the jackal in this study. The species seems to prefer one to two prey items at 80.77%, followed by three and four prey items at 17.31% and 1.92%, respectively. Figure 2 shows the overall scat content of the jackal in GNPS. A relatively large percent showed an occurrence of plant materials (Zizyphus spp. and Caparis spp.). The remains of mammalian prey items seen in the scats of jackal included those of Chital Axis axis, Sambar Rusa unicolor, Buffalo Bubalus sp., Indian Hare Rufus nigricollis, Cow Bos indicus, rodents, Hanuman Langur Semnopithecus entellus and Bluebull Boselaphus tragocamelus (Table 2). Chital, Buffalo and hare seem to be preferred mammalian prey species covering around 72.84% of the jackal diet. The contribution of wild and domestic mammalian prey in the diet of jackals in GNPS was observed as 67.9% and 32.1%, respectively.

Large mammals were the preferred prey group of the jackal, observed from the scat analysis (Fig. 3). Plant material has a relatively high frequency of occurrence compared to other food groups showing the relative importance of the plant material in the diet of the jackal in GNPS. The occurrence of plant material is not detected in all the scats of the jackal despite being a relatively important food source. This may have been due to the temporal availability of fruits in GNPS.








Scat analysis has been used in a wide variety of canid species to infer dietary composition (Schaller 1967; Jethva & Jhala 2004; Giannatos et al. 2005; Habib 2007; Szabó et al. 2010; Majumder et al. 2011). The dietary composition of jackal has been studied based on the frequency of occurrence and percentage weight of different food items in scats (Giannatos et al. 2005; Szabó et al. 2010; Majumder et al. 2011) as well as direct observations and stomach content analysis (Stoyanov 2012). All these methods have shortcomings. The percent occurrence of a particular food item in scats may differ from actual consumption. Different plant species also vary in their seed size and pulp-seed size ratio, which affects the percent weight. These methods, however, can provide useful insights into the dietary preferences of omnivore species such as the jackal.

Jackal feeds on a variety of food items including plant material like other canids (Jethva & Jhala 2004; Habib 2007). They are opportunistic omnivores and their diets may vary seasonally and geographically (Giannatos 2004; Jhala & Moehlman 2008; Majumder et al. 2011; Stoyanov 2012). In previous studies, it was also found that jackal consumed both animal and plant matter, with variation probably related to food availability (Sillero-Zubiri et al. 2004; Lanszki & Heltai 2010; Majumder et al. 2011). This also confirms the variety of food items including mammals, birds, plant materials (fruits) and human food waste in the diet of jackal.

GNPS being a dry and semi-arid tropical area, the summer starts a little early, and dry fruits left intact in trees are shed owing to a change in wind speed. These fallen dry fruits especially Zizyphus spp. which is high in nutritional value become available to any herbivore species as well as omnivores such as jackal. Similarly, other studies on jackal (Sankar 1988; Balasubramaniam & Bole 1993; Mukherjee et al. 2004; Aiyadurai & Jhala 2006; Majumder et al. 2011) also reported the same finding along with studies on other omnivores that found the occurrence of plant matter (Gopal 1991). The jackals remain active during the day, which allows them to search for food in larger areas and scavenge on carcasses of large mammals such as chital, sambar, bluebull, hare and langur. Jackals are group hunting canids (Lanszki & Heltai 2010). The observed hairs of Chital and Indian Hare in the jackal diet might also be a result of predation on chital fawn and hares. Jackals carrying hares and remains of chital fawn in daylight were observed several times during the field work in the GNPS (Image 1–3). On several occasions, groups of jackals were found chasing chital fawns. There are many Maldhari Nesses distributed throughout the Gir Sanctuary, and the observed occurrence of livestock remains in jackal scats during the study period were possibly due to scavenging on the carcasses of livestock from these Nesses and possibly also from the surrounding villages.






In GNPS, both animal and plant matter contribute to the diets of jackal. The considerable presence of plant matter in the diet of the jackal confirmed that plants might play an important role in fulfilling their nutritional requirements. The low content of birds in the scats was in accordance with the evidence of low bird consumption outside the nesting season found in most studies (Demeter & Spassov 1993). The content of rodents found in jackal scats in this study confirmed the significance of rodents as a prey item throughout the year. Utilization of small mammals by jackal was also reported in numerous studies in Asia (Demeter & Spassov 1993; Mukherjee et al. 2004; Jaeger et al. 2007), Africa (Lamprecht 1978) and European agricultural area (Lanszki et al. 2006; Lanszki & Heltai 2010), and this food type is clearly preferred by the jackal (Lanszki & Heltai 2010). The presence of domestic mammals in the scat remains also reveals the tendency of jackal to frequent human settlements and nesses in search of food reflecting dependency of these animals on human leftovers.

In conclusion, the primary food of jackal consisted of large animals (carcass of large animals are scavenged) to medium size to small animals (small animals are hunted), as well as plant material (mainly fruits) in the GNPS. A long term ecological study is required on this meso-carnivore to examine the implications of the diet profiles of different carnivore species and temporal activity for understanding resource partitioning patterns and sympatricity among them in GNPS.




Ackerman, B.B., F.G. Lindzey & T.P. Hernker (1984). Cougar food habits in southern Utah. Journal of Wildlife Management 48(1): 147– 155.

Aiyadurai, A. & Y.V. Jhala (2006). Foraging andhabitat use by Golden Jackals (Canis aureus) in the Bhal region, Gujarat India. Journal of the Bombay Natural History Society 103(1): 1.

Alam, M.S. (2010). First record of Lesser False Vampire Bat (Magaderma spasma) in Gir National Park and Sanctuary. Journal of the Bombay Natural History Society 107(2): 155–156.

Alam, M.S. (2011). Status ecology and conservation of Striped Hyena (Hyaena hyaena) in Gir National Park and Sanctuary, Gujarat. PhD Thesis. Aligarh Muslim University, Aligarh, India.

Alam, M.S., J.A. Khan, S.P.S. Kushwaha, R. Agrawal, B.J. Pathak & S. Kumar (2014). Assessment of suitable habitat of near threatened Striped Hyena (Hyaena hyaena Linnaeus, 1758) using remote sensing and geographic information system. Asian Journal of Geoinformatics 14(2): 1–10.

Balasubramaniam, P. & P.V. Bole (1993). Seed dispersal by mammals at Point Calimere Wildlife Sanctuary, Tamil Nadu. Journal of the Bombay Natural History Society 90: 33–44.

Champion, H.G. & S.K. Seth (1968). A Revised Survey of the Forest Types of India. Manager of Publications, Govt. of Indian Press, New Delhi, 404pp.

Corbett, L.K. (1989). Assessing the diet of dingoes from feces: a comparison of three methods. Journal of Wildlife Management 53(2): 343–346.

Demeter, A. & N. Spassov (1993). Canis aureus Linnaeus, 1758. Handbuch der Säugetiere Europas 5: 107–138.

Floyed, T.G., L.D. Mech & P.J. Jordan (1978). Relating wolf scat content to prey consumes. Journal of Wildlife Management 42(3): 528–532.

Fowler, J., L. Cohen & P. Jarvis (2006). Practical Statistics for Field Biology. Jhon Wiley & Sons, England, 259pp.

Giannatos, G. (2004). Conservation Action Plan for the Golden Jackal Canis aureus L. in Greece. WWF Greece, 47pp.

Giannatos, G., Y. Marinos, P. Maragou & G. Catsadorakis (2005). The status of the Golden Jackal (Canis aureus L.) in Greece. Belgian Journal of Zoology 135(2): 145–149

Gopal, R. (1991). Ethological observations on the Sloth Bear (Melursus ursinus). Indian Forestor 117: 915–920.

Habib, B. (2007). Ecology of Indian Wolf (Canis lupus pallipes Skyes, 1831) and modelling its potential habitat in the Great Indian Bustard Sanctuary, Maharashtra, India. PhD Thesis. Department of Wildlife Sciences, Aligarh Muslim University, Aligarh, India.

Jaeger, M., E. Haque, P. Sultana & R. Bruggers (2007). Daytime cover, diet and space-use of Golden Jackals (Canis aureus) in agro-ecosystems of Bangladesh. Mammalia 71: 1–10; http://dx.doi. org/10.1515/MAMM.2007.016

Jethva, B.D. & Y.V. Jhala (2003). Sample size consideration for food habits studies of wolfs from scats. Mammalia 68(4): 589–591;

Jethva, B.D. & Y.V. Jhala (2004). Foraging ecology, economics and conservation of Indian wolves in the Bhal region of Gujarat, Western India. Biological Conservation 116: 351–357.

Jhala, Y.V.& P.D. Moehlman (2008). Canis aureus. In: IUCN 2013. IUCN Red List of Threatened Species. Version 2013.2. <www.iucnredlist. org>. Downloaded on 29 January 2014.

Khan, J.A., R. Chellam, W.A. Rodgers & A.J.T. Johnsingh (1996). Ungulate density and Biomass in the tropical dry deciduous forest of Gir, Gujarat, India. Journal of Tropical Ecology 12(1): 149–162;

Korschgen, L.K. (1980). Procedure for food habits analysis, pp. 113–128. In: Schemnitz, S.D. (ed.). Wildlife Management Techniques Manual. The Wildlife Society Washington, D.C.: 113-128

Katuwal, H.B. & S. Dahal (2013). Golden Jackals in human dominated landscapes of the Manaslu Conservation Area, Nepal. Vertebrate Zoology 63(3): 329–334

Lamprecht, J. (1978). On diet, foraging behaviour and inter specific food competition of jackals in the Serengeti National Park, East Africa. Mammalian Biology 43: 210–223.

Lanszki, J., M. Heltai & L. Szabó (2006). Feeding habits and trophic niche overlap between sympatric Golden Jackal (Canis aureus) and Red Fox (Vulpes vulpes) in the Pannonian ecoregion (Hungary). Canadian Journalof Zoology 84(11): 1647–1656;

Lanszki, J. & M. Heltai (2010). Food preferences of Golden Jackals and sympatric Red Foxes in European temperate climate agricultural area (Hungary). Mammalia 74: 267–273; MAMM.2010.005

Leopold, B.D. & P.R. Krausman (1986). Diet of 3 predators in Big Bend National Park, Texas. Journal of Wildlife Management 50: 290-295.

Lockic, J.D. (1959). The estimating of the food of Foxes. Journal of Wildlife Management 23(2): 224–231.

Macdonald D.W. (1983). The ecology of carnivore social behaviour. Nature 301: 379–383;

Macdonald, D. (1984). The Encyclopaedia of Mammals. Greenwich Editions, London, 154–159pp.

Majumder, A., K. Sankar, Q. Qureshi & S. Basu (2011). Food habits and temporal activity patterns of the Golden Jackal Canis aureus and the Jungle Cat Felis chaus in Pench Tiger Reserve, Madhya Pradesh, India. Journal of Threatened Taxa 3(11): 2221–2225; http://dx.doi. org/10.11609/JoTT.o2713.2221-5

Meena, R.L. & S. Kumar (2012). Management Plan for Gir Protected Areas. Volumes 1 & 2. Gujarat Forest Department, Gujarat, India, 281pp.

Mukherjee, S., S.P. Goyal & R. Chellam (1994). Refined techniques for the analysis of Asiatic Lion Panthera leo persica scats. Acta Theriologica 39: 425–430.

Mukherjee, S., S.P. Goyal, A.J.T. Johnsingh & M.R.P.L. Pitman (2004). The importance of rodents in the diet of Jungle Cat (Felis chaus), Caracal (Caracal caracal) and Golden Jackal (Canis aureus) in Sariska Tiger Reserve, Rajasthan, India. Journal of Zoology 262(04): 405–411;

Prater, S.H. (1980). The Book of Indian Animals. Bombay Natural History Society, Oxford University Press, Bombay, 263pp.

R - Development Core Team (2008). R: A language and environment for statistical computing. R- Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0, URL http://www.R-project. org

Reynold, J.C. & N.J. Aebischer (1991). Comparison and quantification of carnivore diet by fecal analysis: a critique, with recommendation, based on study of the Fox Vulpes vulpes. Mammal Review 21(3): 97–122; http://

Russev, Y. (2010). Status of game stocks in Bulgaria. Forest 6(7): 34–36.

Sankar, K. (1988). Some observations on food habits of Jackal (Canis aureus) in Keoladeo National Park, Bharatpur, as shown by scat analysis. Journal of the Bombay Natural History Society 85(1): 185– 186.

Schaller, G.B. (1967). The deer and the tiger. A study of wildlife in India. University of Chicago Press, Chicago, IL, 70pp.

Sillero-Zubiri, C., M. Hoffmann & D.W. Macdonald (2004). Canids: Foxes, Wolves, Jackals and Dogs. Status Survey and Conservation Action Plan. IUCN/SSC Canid Specialist Group, Gland & Cambridge, 430pp.

Singh, H.S. & R.D. Kamboj (1996). Biodiversity Conservation Plane for Gir. Vol. - I. Gujarat state Forest Department, India, 242pp.

Singh, H.S. & L. Gibson (2011). A conservation success story in the otherwise dire megafauna extinction crisis: The Asiatic Lion (Panthera leo persica) of Gir forest. Biological Conservation 144(5): 1753–1757; http://

Stoyanov, S. (2012). Golden Jackal (Canis aureus) in Bulgaria: current status, distribution, demography and diet. International symposium on hunting, Мodern aspects of sustainable management of game population. Zemun-Belgrade, Serbia, 22–24.

Szabó L., M. Heltai & J. Lanszki (2010). Jackal versus livestock - Is it a real problem? Hungarian Agricultural Research 19(4): 4–10.

The Wildlife (Protection) Act (1972). As Amended up to 2002. Natraj Publishers, Dehradun.

Weaver, J. & S. Fritts (1979). Comparison of Coyote and Wolf scat diameters. Journal of Wildlife Management 43(3): 786–788

Yom-Tov Y., S. Ashkenazi & O. Viner (1995). Cattle predation by the Golden Jackal Canis aureus in the Golan Heights, Israel. Biological Conservation 7(1): 19–22;