Journal of Threatened
Taxa | www.threatenedtaxa.org | 26 February 2026 | 18(2): 28399–28405
ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.10059.18.2.28399-28405
#10059 | Received 24 July 2025 | Final received 14 January 2026 | Finally
accepted 28 January 2026
Population status and habitat use
of Indian Grey Wolf Canis lupus pallipes in Pench Tiger
Reserve, Madhya Pradesh, India
Iqra Rabbani 1 & Sharad Kumar 2
1,2 Department of Wildlife Sciences,
Aligarh Muslim University, Aligarh, Uttar Pradesh, India.
1 rajputiqrarabbani@gmail.com, 2
sharadamu@gmail.com (corresponding author)
Editor: Murali Krishna Chatakonda, Amity University, Noida, India. Date of publication: 26 February 2026 (online & print)
Citation:
Rabbani, I. & S. Kumar (2026). Population status and habitat use of
Indian Grey Wolf Canis lupus pallipes in Pench Tiger
Reserve, Madhya Pradesh, India. Journal of
Threatened Taxa 18(2):
28399–28405. https://doi.org/10.11609/jott.10059.18.2.28399-28405
Copyright: © Rabbani & Kumar 2026. Creative Commons Attribution 4.0 International License.
JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: None.
Competing interests: The authors declare no competing interests.
Author details: Iqra Rabbani is a PhD research scholar in the Department of Wildlife Sciences at Aligarh Muslim University, Aligarh, Uttar Pradesh, India. Her research focuses on wolf ecology and habitat studies, species distribution, and conservation. Dr. Sharad Kumar is working as assistant professor in Department of Wildlife Sciences at Aligarh Muslim University. He has conducted long-term research on tiger ecology in Corbett Tiger Reserve. He has also been actively involved in various wildlife research and conservation programs across Uttarakhand, Madhya Pradesh, Gujarat, and Assam, contributing significantly to large carnivore conservation efforts in India.
Author contributions: Concept and design of study IR and SK. Supervision: SK. Data collection: IR. Analysis: IR and SK. Manuscript writing IR, Manuscript review and comments: IR and SK.
Acknowledgements: We sincerely express our gratitude to the Forest Department of Pench Tiger
Reserve for their continuous support and cooperation during my study. We are especially grateful to Shri Rajnish Singh, IFS, Deputy Director granting permission to conduct research and for his constant guidance and logistical support throughout fieldwork. We also extend our sincere thanks to Shri Sumit Rega, Shri Rahul Upadhyaya, and S.K. Ukiye from Forest Department. I (Iqra Rabbani) also thankful to all the faculty members of Department of Wildlife Sciences at Aligarh Muslim University, Aligarh, for their guidance, encouragement, and valuable teachings throughout my academic journey. Finally, I wholeheartedly thankful to Vikrant Sharma, Ananya Prasad, Nishat Fatima for their endless support and encouraging me at every step.
Abstract: Wolves, once one of the most
widely distributed carnivores on Earth, have experienced drastic population
declines and range contractions due to anthropogenic pressures. We studied the
population status and habitat utilization of the Indian Grey Wolf in Pench Tiger Reserve (PTR). Both direct and indirect
evidence were used to assess wolf presence, and Bonferroni confidence intervals
were calculated to analyze habitat utilization. Wolf distribution was found to
be restricted to the Khawasa Range of PTR, with the Khawasa Beat showing the highest encounter rate (0.154/km).
Most wolf signs were recorded in mixed habitats (miscellaneous), underscoring
the importance of these areas for the species’ long-term conservation. A
significant positive correlation was observed between tree-cutting and wolf
encounter rate (r = 0.976, p = 0.024, df = 3),
suggesting that habitat changes associated with tree removal may influence wolf
activity.
Keywords: Anthropogenic pressures,
Bonferroni confidence intervals, buffer zone, camera trap, carnivores,
correlation, direct and indirect evidence, encounter rate, grazing,
tree-cutting.
INTRODUCTION
The Grey Wolf Canis
lupus, the largest member of the canid family, inhabits a wide range of
terrestrial ecosystems (Mech 1974; Jhala & Giles
1991). Its global distribution spans across 68 countries, making it one of the
most widely distributed terrestrial mammals (Boitani
et al. 2020). Among the 10 subspecies of Grey Wolf recognized worldwide (Boitani et al. 2020; Werhahn
2020), India harbors two distinct subspecies: the Himalayan or Tibetan Wolf Canis lupus chanco
and the Indian Grey Wolf or Indian Peninsular Wolf Canis
lupus pallipes (Aggarwal et al. 2003; Sharma et
al. 2004). The Indian Grey Wolf is a keystone carnivore of India’s semi-arid
and grassland ecosystems. Despite its ecological significance, the taxon
remains one of the least studied large carnivores in the country, often
overshadowed by charismatic megafauna such as the elephant, tiger, and leopard.
In India, the Indian Grey Wolf is protected under Schedule I of the Wildlife
(Protection) Act, 1972 and is listed as ‘Vulnerable’ by the IUCN as its
populations are considered fragmented and declining due to increasing
anthropogenic pressures (IUCN 2025).
Over the past few decades, the
global decline of large carnivores has emerged as a critical conservation
issue, with many species experiencing significant range contractions and
population losses (Weber & Rabinowitz 1996; Ripple et al. 2014; Fernández-Sepúlveda & Martín 2022). The Indian Grey Wolf is no
exception, having suffered a substantial decline across much of its historical
distribution (Mech 1970). This decline has been largely attributed to habitat
degradation, increasing human-wolf negative interactions, low public awareness,
and in some areas, targeted persecution and extermination campaigns (Habib
2007). The estimated population of the Indian Grey Wolf in India is around
3,170 individuals (Jhala et al. 2022), distributed across
fragmented habitats with little to no connectivity between metapopulations.
This highlights the urgent need for region-specific conservation strategies
tailored to local ecological and sociopolitical contexts. It is estimated that India has a total of
89,138 km2 suitable habitats for breeding packs; the largest
continuous breeding habitat is located in the Central Indian landscape (Jhala et al. 2022).
The remaining populations of the Indian Grey Wolf are small, fragmented,
and increasingly isolated, making them highly vulnerable to local extinction.
Without targeted management interventions and scientific understanding of their
population status and habitat needs, the long-term viability of these
populations remains at risk (Singh & Kumara 2006;
Becker et al. 2008).
Reliable information on
population size and habitat use is essential for the effective conservation of
any threatened species (Sousa-Silva et al. 2014). Acquiring such data is
particularly challenging for species like the Indian Grey Wolf, which occur at
low densities and inhabit vast, human-dominated landscapes (Mahajan et al.
2022a). Although several studies have assessed the species’ status at local and
regional scales (Jhala & Giles 1991; Kumar & Rahmani 1997; Kumar 1998; Singh & Kumara
2006), and a few at the national level (Shahi 1982; Jhala
1993, 2003; Karanth et al. 2009; Srivathsa
et al. 2020; Jhala 2022), knowledge gaps still
persist regarding their ecological preferences across different landscapes.
Pench Tiger Reserve (PTR), located in
the Satpura-Maikal landscape of central India, is a
known stronghold for apex predators like the Bengal Tiger Panthera
tigris and Leopard Panthera
pardus. However, its role as a habitat for
lesser-known carnivores such as the Indian Grey Wolf is poorly understood.
Understanding the population status and habitat utilization patterns of the
Indian Grey Wolf in a multi-use landscape of PTR is crucial for informed conservation
and management efforts. This study aims to assess the current distribution and
habitat preferences of the Indian Grey Wolf within Pench
Tiger Reserve, Madhya Pradesh. By identifying key habitats and anthropogenic
influences, the findings will contribute to evidence-based strategies for the
conservation of this ecologically important yet vulnerable carnivore.
MATERIAL AND METHODS
Study Area
The study was conducted in PTR,
located in the central Indian state of Madhya Pradesh (Figure 1). The Reserve
spans an area of 1,179.63 km² and falls within the Seoni
and Chhindwara districts. Geographically, PTR lies
between 78.916–79.583 0E and 21.583–22.000 0N. The
elevation ranges 425–600 m. Although some areas like the Karmajhiri
Range are plains, the majority of PTR’s terrain is characterized by gently
undulating landscapes interspersed with seasonal streams and ‘nallahs’. The region experiences a wide temperature range,
from 0°C in winter to 45°C in summer (Sankar et al.
2000), with an average annual rainfall of approximately 1,300 mm. The climate
is marked by four distinct seasons: summer (March–June), monsoon (July–August),
post-monsoon (September–November), and winter (December–February).
The vegetation in Pench Tiger Reserve is predominantly composed of dry
deciduous forests, comprising pure Teak Tectona
grandis forest, Teak-mixed forest, mixed forests,
bamboo forest, and open grasslands. The reserve supports a diverse assemblage
of carnivores, including the Tiger, Leopard, Dhole Cuon
alpinus, Jungle Cat Felis
chaus, Small Indian Civet Viverricula
indica, Sloth Bear Melursus
ursinus, Golden Jackal Canis
aureus, Indian Grey Wolf, and Common Palm Civet Paradoxurus
hermaphroditus. The herbivore community includes
species such as the Sambar Rusa unicolor,
Chital or Spotted Deer Axis axis, Gaur Bos gaurus, Nilgai Boselaphus
tragocamelus, and Chousingha
or Four-horned Antelope Tetracerus quadricornis. In addition to mammals, the reserve hosts
a rich diversity of birdlife, with over 250 recorded species.
Methods
Camera-trapping data in 2019–2023
were collected from the forest department of Pench
Tiger Reserve. Data analysis revealed the presence of the Indian Grey Wolf
exclusively in the Khawasa Range of the Reserve.
Accordingly, the Khawasa Range was selected for
further data collection (January–March 2023) on population status and habitat
use of wolves. The range is a multi-use area of the Reserve and predominantly
characterized by tropical dry deciduous forest. The vegetation is dominated by
Teak along with associated species such as Mahua Madhuca
indica, Saja Terminalia
tomentosa, and Tendu Diospyros
melanoxylon. The range experiences moderate level
of human disturbance like livestock grazing, tree-lopping, and the seasonal
collection of forest products like Mahua flowers and Tendu
leaves. The range comprises nine forest beats, each of which was chosen as a
sampling unit to assess the population status and habitat utilization patterns
of the species.
Wolf status and habitat use
across forest beats were assessed by systematically searching for and recording
both direct and indirect evidences of wolves. Surveys were conducted along all
trails, roads, and nallahs within the different
beats, as these features are commonly used by wolves for movement within their
home ranges. Survey efforts involved walking 171 km² across these features.
This approach increases the probability of detecting wolf evidence compared to
random surveys (Mahajan et al. 2022b). To minimize bias arising from
misidentification, only fresh signs were recorded during the survey.
Whenever direct or indirect
evidence of wolves was encountered, data on evidence type, location, habitat,
terrain and status of anthropogenic pressures were collected. To differentiate
indirect evidence of the Indian Grey Wolf from those of related sympatric
species such as the Domestic Dog Canis familiaris and Golden Jackal Canis
aureus, we compared pugmarks, scats, and associated field signs during
surveys. Wolf pugmarks are large (7–10 cm in length), oval and symmetrical
shape with a straight posterior margin of the heel pad, whereas dog tracks are
more variable in size, often rounder and asymmetrical with prominent claw
impressions, and jackal tracks are smaller (4.5–6 cm), compact, and narrower
(Talwar & Usmani 2005; Mahajan et al. 2022b).
Scats were distinguished based on size, shape, and contents. The wolf scats are
thick (2–3 cm diameter), rope-like, and generally contained hair, bones, and
prey remains; dog scats are irregular, softer, and often contained
anthropogenic matter; jackal scats are smaller (1.5–2 cm diameter), segmented,
and frequently contained fruit seeds in addition to hair (Jhala
2003; Rather 2021; Mahajan et al. 2022b). Data from camera-trapping and
evidence surveys were used for the analysis of habitat use.
To quantify habitat conditions
and habitat use, random sampling plots were laid in each beat. For the
tree-layer assessment, a circular plot with a 10-m radius was used. Within
this, a nested 5-m radius circular plot was laid to assess the shrub layer
following Haleem & Ilyas (2023). The data collected from these plots were
used to quantify vegetation characteristics, including species density,
diversity, richness, and evenness, which were then used to understand patterns
of wolf habitat utilization. The area under different habitat types was
determined using Remote sensing and geographic information system (GIS)
analysis based on the land use and land cover (LULC) map of the study area.
Analysis
The trails were monitored once,
covering a total distance of 171 km. Beat-wise encounter rates were calculated
by dividing the total number of wolf evidence recorded in each beat by the
total distance travelled within that beat (Table 1). To evaluate the relationship
between anthropogenic pressures and wolf presence, non-parametric correlation
analysis was conducted using SPSS version 22.0 (IBM Corp 2013). Vegetation
attributes, including tree and shrub diversity, richness, and evenness, were
computed using PAST software.
Data on direct and indirect wolf
evidence were segregated by habitat type. A chi-square test was performed to
examine whether the distribution of wolf evidence differed significantly among
the various habitat types. To assess habitat use patterns
by wolves, Bonferroni confidence intervals were calculated (Neu et al. 1974;
Byres et al. 1994). Habitat preferences and avoidance were determined based on
these intervals.
RESULTS
Over the past five years, a total
of 27 camera-trap captures of the Indian Grey Wolf were recorded in the Khawasa Range. The camera trap data revealed the presence
of wolves in six out of nine beats of Khawasa range: Kothar, Amajihri, Amabari, Teliya, Vijaypani, and Khawasa. No wolf
detections were recorded in East Kohka, Mohgaon, and Pipariya beats.
Among the beats where wolves were captured, Kothar
Beat recorded the highest number of captures, while Amajihri
and Teliya had the lowest (Figure 2).
A total of 13 direct and indirect
signs of Indian Grey Wolf presence were recorded during the sign survey,
confirming their occurrence in only four out of the nine beats of the Khawasa Range. The highest encounter rate was recorded in
the Khawasa Beat (0.15 evidences/km), while the
lowest was in Pipariya Beat (0.12 evidences/km)
(Table 1). The analysis of anthropogenic pressures in beats with wolf presence
revealed varying intensities of human activities. The highest tree-lopping was
recorded in Pipariya Beat (95 trees/ha) while the
lowest was in Khawasa Beat. The highest tree-cutting
was recorded in Khawasa (81.9 trees/ha), whereas Pipariya Beat had the lowest tree-cutting. The highest
intensity of grazing was recorded in Vijaypani while
there was no grazing in Aamajhiri (Table 1). No significant correlation was observed between
the wolf encounter rate and most anthropogenic pressures, except for
tree-cutting, which showed a strong positive correlation with encounter rate (r
= 0.976, p = 0.024, df = 3).
In terms of shrub composition,
Ambari had the highest shrub diversity (1.673), while East Kohka
showed the highest shrub richness (1.593), and Ambari again had the highest
shrub evenness (0.7608). Conversely, the lowest shrub diversity was observed in
Kothar (1.022), lowest richness in Mohgaon (1.027), and lowest evenness in Kothar
(0.3968) (Table 2).
Habitat-wise comparison of
vegetation parameters revealed that the mixed habitat (Miscellaneous Forest)
had the highest tree diversity (2.84), richness (4.345) and evenness (0.5351),
which indicates species in mixed habitats are more evenly distributed than in
Teak and Teak-mixed habitat (Table 3). Analysis of 40 wolf evidences (including
camera-trap captures) across three habitat types – mixed, teak mixed, and teak
– revealed that the majority of evidence (32) was recorded from mixed habitat,
while Teak and Teak-mixed habitats each had four evidences. A chi-square test
indicated no statistically significant difference in habitat utilization by the
Indian Grey Wolf (χ² = 4.9, df = 2, p = 0.05),
although the test statistic was close to the critical value. To further assess
habitat preference, Bonferroni confidence intervals were calculated (Table 3).
The results suggested that Teak habitat was utilized less than its
availability, whereas mixed and Teak-mixed habitats were used in proportion to
their availability.
DISCUSSION
This study revealed that the
distribution of the Indian Grey Wolf in PTR is restricted to the Khawasa Range, which lies in the buffer zone, with most
sightings occurring near human settlements. Their absence from the core area
and exclusive presence in the buffer zone aligns with findings by Jhala et al. (2022), who suggest that wolves prefer
habitats with low to moderate densities of dominant predators such as tigers
and leopards. This avoidance may be attributed to the high density of tigers
and leopards in the core zone of the study area, indicating that wolves
actively avoid areas dominated by larger carnivores. The proximity of wolf
sightings to human settlements suggests opportunistic behaviour,
likely driven by availability of livestock carcasses and anthropogenic waste
near human settlements, an adaptive trait also documented in other studies (Jethva & Jhala 2004; Becker
et al. 2008; Sharma et al. 2019). By utilizing consistent and energy-efficient
food sources such as livestock carcasses and human waste, wolves may compensate
for limited access to wild prey resulting from interference or competition with
dominant carnivores (Becker et al. 2008).
Habitat composition also plays a
significant role in influencing wolf distribution in the study area. Results of
the study indicate a preference for mixed and Teak-mixed forest types, which
provide both concealment and prey opportunities. These habitats tend to support
higher densities of herbivores due to their diverse ground vegetation and
structural complexity (Karanth & Sunquist 1995), thereby indirectly benefiting wolves.
The significant positive
correlation between tree-cutting and wolf encounter rate indicates that higher
tree felling is associated with increased wolf activity. Tree-cutting creates
open spaces and such areas also have more dirt roads and trails, which may
facilitate wolf movement and improve hunting efficiency by increasing prey
visibility and accessibility. Additionally, tree-cutting can enhance the growth
of ground vegetation (shrub and herb layers). This improved ground cover may
further contribute to habitat suitability by supporting higher prey abundance
and enhancing foraging opportunities for wolves. This pattern highlights the
species’ ability to exploit human-modified habitats. Similar findings have been
reported in other studies, where wolves were observed to use logging roads,
clear-cuts, and other disturbed habitats to optimize travel and foraging
efficiency (Whittington et al. 2005; Houle et al. 2010). Therefore, the
observed relationship may reflect a functional response of wolves to
human-mediated habitat changes, demonstrating their adaptability in
human-dominated landscapes.
Study findings highlight that
buffer zones are not merely peripheral spaces but serve as critical habitats
for many wildlife species, including wolves. These areas must be recognized for
their ecological value and managed accordingly. An effective conservation
strategy should integrate habitat management, scientific research, and active
community participation to ensure the protection of wildlife across the
landscape. To ensure the long-term conservation of wolves in the region, it is
essential to adopt a landscape-level conservation approach. Given that wolf
packs require large home ranges, ranging 150–300 km2 (Jhala 2003; Habib 2007), focusing solely on small habitat
patches is insufficient. Conservation efforts should prioritize the protection
of natural habitat features and the maintenance of wildlife corridors, enabling
free movement between areas and promoting population connectivity (Sharma et
al. 2019; Gubbi et al. 2020).
Table 1. Status of
the anthropogenic pressures in beats with wolf presence in Pench Tiger Reserve.
|
Beats |
Wolf encounter rate
(evidence/km) |
Tree-lopping density (ha) |
Tree-cutting density (ha) |
Cattle dung piles density (ha) |
|
Khawasa |
0.154 |
40.9 |
81.9 |
22.7 |
|
Aamajhiri |
0.137 |
47.8 |
15.9 |
0.0 |
|
Pipariya |
0.121 |
95.5 |
15.9 |
79.6 |
|
Vijaypani |
0.141 |
63.7 |
31.8 |
111.5 |
Table 2. Habitat-wise
tree and shrub indices and
counts of wolf evidence in Pench Tiger Reserve.
|
Habitat |
Tree diversity |
Tree richness |
Tree evenness |
Shrub diversity |
Shrub richness |
Shrub evenness |
Wolf evidence |
|
Mixed |
2.84 |
4.345 |
0.5351 |
0.811 |
1.957 |
0.5144 |
32 |
|
Teak |
1.687 |
3.049 |
0.2843 |
0.8107 |
2.213 |
0.654 |
4 |
|
Teak Mixed |
2.02 |
3.717 |
0.3428 |
0.5522 |
0.9128 |
0.5508 |
4 |
Table 3. Availability
and expected proportional usage with 95% Bonferroni confidence intervals.
|
Habitat |
Observed usage |
Expected usage |
Actual proportional use (Pi) |
Expected proportional use (Pio) |
Bonferroni confidence
interval |
Remark |
|
Mixed |
32 |
26.96 |
0.8 |
0.67 |
0.654 ≤ Pi ≤ 0.945 |
0 |
|
Teak |
4 |
10.02 |
0.1 |
0.25 |
-0.009 ≤ Pi ≤ 0.209 |
- |
|
Teak mixed |
4 |
3.005 |
0.1 |
0.07 |
-0.009 ≤ Pi ≤ 0.209 |
0 |
-—Avoided | +—Preferred | 0—used
in accordance to availability.
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