Assessing Avian Biodiversity and Conservation Challenges in A Semi-Arid Hill Ecosystem: A Case Study from The Harsh-Jeen Region
Abhishek Rollan¹, Dr. Nisha Siroya2, Dr. A. K. Siroya³
¹Research scholar, Department of Zoology, S.P.C. Govt. College, Ajmer (Rajasthan)
²Associate Professor, Department of Zoology, S.P.C. Govt. College, Ajmer (Rajasthan)
³Professor, Department of Zoology, S.P.C. Govt. College, Ajmer (Rajasthan)
DOI: https://doi.org/10.51244/IJRSI.2025.120600146
Received: 12 June 2025; Accepted: 20 June 2025; Published: 17 July 2025
It is critical for conservation to comprehend how elevation affects avian biodiversity, particularly in ecologically delicate and little understood semi-arid areas. In this study, the HARSH-JEEN hills of Rajasthan, which are a component of the Aravalli range, are examined for their bird population composition, distribution patterns, and anthropogenic stresses along an elevation gradient (350–800 m). We documented 42 families and 122 species using routine field surveys conducted throughout the year using line transect and point count techniques. The species richness distribution was unimodal, peaking at mid-elevations (500–650 m). Elevation specialists included a number of species of conservation interest. Zones of high religious tourism and vegetation loss were found to be significantly fragmented in low- and mid-elevation zones, according to a GIS-based land cover analysis. Initial community interviews also revealed a decline of traditional management and an increase in anthropogenic hazards. The necessity of site-specific conservation strategies, such as habitat zoning, community-based stewardship models, and sustainable ecotourism activities, is highlighted by the present research. A reproducible model for comparable dryland hill ecosystems throughout the Aravalli region is provided by these results.
Keywords: Avian biodiversity, HARSH-JEEN hills, Semi-arid ecosystem, Species richness, Habitat fragmentation, GIS mapping, Community perception, Rajasthan birds, Conservation strategy.
Particularly in areas that are under environmental stress, research on elevation-driven biodiversity patterns is critical for understanding ecological processes, species distribution, and conservation planning (Rahbek, 2005).
Mountains provide a unique chance to study these patterns because of their diverse flora kinds and microclimates. However, dry and semi-arid mountain systems have not received enough attention in this study, with most of it concentrating on tropical and temperate regions (Price et al., 2011).
A semi-arid hill habitat, the HARSH and JEEN hills are situated in Rajasthan, India’s Sikar district and are a component of the Aravalli range. Scrublands, grasslands, scant woods, and places of worship are among the many ecosystems found on these hills. Both permanent and few migratory species may be supported by a diverse avifaunal population because of their elevation variety and isolation. The richness of birds in this area is still not well recorded, despite its ecological significance. Furthermore, human activities like religious tourism, deforestation, grazing is putting more and more strain on the region. Our work closes this gap by evaluating bird biodiversity across height gradients in the HARSH-JEEN highlands and identifying critical conservation issues. Examine the functions of particular native bird species in the ecology of the HARSH-JEEN hills. Examine the ways that religious tourism affects environmental preservation and deterioration. Discuss about the connection between the region’s declining bird population and forestry practices. Provide ideas for how to engage nearby communities in conservation initiatives to save the species of birds. Emphasize the importance of HARSH-JEEN hills and effective case studies of conservation initiatives in related natural zones.
Elevation and Biodiversity Patterns: Global Foundations
Ecologists have long recognized the significance of elevation in shaping biodiversity patterns, treating elevational gradients as natural laboratories for exploring how temperature, precipitation, and vegetation structure influence species distribution (McCain, 2009; Rahbek, 1995).
These gradients offer valuable insights into how climatic variables interact with topography to shape species richness and composition. Environmental factors such as productivity, humidity, and habitat heterogeneity are key drivers of these elevational biodiversity patterns (Colwell & Lees, 2000; Körner, 2007)
In recent decades, climate change has emerged as a major factor influencing species distributions along elevational gradients. A growing body of research indicates that many species, particularly birds, are shifting their ranges upward in response to warming temperatures (Forero-Medina et al., 2011; Freeman et al., 2018).
These shifts are particularly pronounced in tropical regions where narrow thermal belts restrict lateral movement, forcing species to ascend to suitable climates. However, for many tropical mountain species with narrow altitudinal ranges, this “escalator to extinction” poses significant threats due to limited habitat at higher elevations (McCain, 2009).
Scale and Spatial Context in Biodiversity Studies
The importance of spatial scale in studying species richness has been widely acknowledged (Rahbek, 2005) emphasized the necessity of fine-scale, site-specific studies, especially in underrepresented ecosystems such as dryland mountain regions. These environments often overlooked in broad-scale conservation assessments, harbour unique species assemblages adapted to extreme and fluctuating conditions.
Indian Context: Conservation in Major and Overlooked Ranges
In India, much of the ornithological focus has traditionally been on the Himalayas and the Western Ghats-regions known for their rich biodiversity and endemic bird populations (Davidar et al., 2001; A. Rahmani et al., 2004).
These studies have laid the foundation for understanding the structure and threats to avian communities in humid mountain systems. However, more recent efforts have begun to spotlight semi-arid and dryland mountain systems, particularly those with socio-cultural importance such as sacred groves. This Studies in highlight how Rajasthan’s semi-arid landscapes-including the Aravalli range-support unique avifaunal diversity (Joshi et al., 2021; Kumar & Koli, 2024).
These regions combine climatic harshness with ecological resilience, creating niches for specialized bird communities. Importantly, many of these species exhibit altitudinal specialization, limiting their distributions to narrow elevation bands and increasing their vulnerability to environmental changes (McCain, 2009).
The HARSH-JEEN Hills: A Neglected Biodiversity Frontier
The Aravalli hills, among the oldest mountain systems in India, remain underrepresented in ornithological literature despite their ecological and geological importance. Recent studies suggest that a variety of bird species that are suited to both dry and elevated environments may be found in the HARSH-JEEN hills, which are a component of the Aravalli range. However, no recent scientific evaluations have looked closely at this field, leaving information gaps that prevent avian bird conservation.
Anthropogenic pressures, including religious tourism, agricultural expansion, and deforestation, exacerbate the vulnerability of dryland mountain birds. These human impacts often overlap with areas of high avian diversity, intensifying conservation challenges. According to this study dryland mountain forests require location-specific protection strategies due to their heightened susceptibility to such threats (Price et al., 2011).
Biotic Interactions and Elevational Shifts:
The importance of biotic interactions in determining bird diversity over elevational gradients has been brought to light by recent research. In the Indian mountain ranges, competition from Oecophylla ants at lower elevations is forcing insectivorous birds to higher altitudes, according to a 2024 research from the Indian Institute of Science. This change highlights the intricate relationship between species interactions and elevational distribution, indicating that both biotic and abiotic variables play a significant role in generating patterns of species richness in mountainous areas (Srinivasan et al., 2024).
Climate-Induced Population Dynamics in Tropical Mountains:
This research, which was carried out on KENYA’s MT. KASIGAU between 2011 and 2023, found that although several bird populations were constant, certain species had notable drops in 2015 and 2022. The fact that these variations were ascribed to environmental in the weather showed how susceptible tropical mountain birds are to changes in the climate. The results highlight the significance of on-going observation in order to comprehend and lessen the effects of climate change on mountain avifauna (Wambugu et al., 2025).
Anthropogenic Threats: Logging and Habitat Degradation:
According to this study, which was carried out in the Eaglenest Wildlife Sanctuary in Arunachal Pradesh, India, logging lowers biodiversity overall and causes the extinction of large-bodied birds that depend on old growth. The decline in foliage-dwelling insect populations in logged forests has a particularly negative impact on understory insectivores, which are niche-dependent. The results highlight how crucial it is to protect primary forests in order to lessen the impact of climate change on montane bird species (Chanda et al., 2023).
Conservation Frameworks and National Policy Insights:
The identification of Important Bird Areas (IBAs) under human stress has reinforced the need for evidence-based conservation interventions (A. Rahmani et al., 2004).
More recently, study have emphasized the role of birds as ecological indicators and cultural symbols, making them ideal subjects for assessing the health of ecosystems. The State of India’s Birds report provides detailed assessments of distribution, abundance, and threat levels across species, offering a comprehensive framework for national-level conservation efforts. (A.R.Rahmani, 2022; Rahul Kishore Talegaonkar, 2023).
The Way Forward: Filling Gaps through Site-Specific Research:
This research in note, arid regions often shows high variability in bird abundance and diversity. Some species may dominate particular habitats while others remain scarce, making habitat-specific studies critical (Sivaperuman et al., 2009).
The HARSH-JEEN hills exemplify such complexity. Despite their potential as biodiversity hotspots, they lack sufficient ornithological data. By integrating elevation data, biodiversity trends, and anthropogenic pressures, the present study aims to bridge this knowledge gap and contribute to evidence-driven habitat management in dryland mountain ecosystems.
Study Area:
The HARSH and JEEN hills, which are between 350 and 800 meters high, are situated in Rajasthan’s Sikar district. Seasonal monsoon rains have an impact on the area’s dry deciduous woodland, scrublands, grasslands, and agricultural regions.
Ecosystems Surveys:
Sampling Design:
Community Interviews:
Semi-structured interviews (n = 25) were conducted with local residents, temple staff, and forest personnel to understand:
GIS and Remote Sensing: Tools Used Sentinel-2 satellite data, QGIS
Data Analysis:
Table 1: Avian Diversity Indices across Elevation Zones in Harsh- Jeen Hills:
| Elevation Zone | Species Richness | Shannon Index | Simpson Index |
| Low (350–500 m) | 61 | 2.89 | 0.87 |
| Mid (500–650 m) | 78 | 3.61 | 0.94 |
| High (650–800 m) | 67 | 3.12 | 0.90 |
Table 2: Regression Analysis:
| Model | R² | p-value | Interpretation |
|
Species Richness~ Elevation |
0.62 | < 0.01 |
Significant positive correlation between elevation and species richness, peaking at mid-elevation.
|
The regression confirms elevation as a major factor influencing avian richness, supporting the mid-domain hypothesis.
In overall altitude zones, 122 bird species from 42 families are identified throughout the year-long investigation. In contrast to 61 species at low altitudes (350–500 m) and 67 species at high altitude (650–800 m), species richness exhibited a single-modal distribution, peaking at mid-elevations (500–650 m) with an average of 78 species. This distribution supports the mid-domain effect hypothesis, which predicts a richness peak at intermediate altitudes. Higher elevations were home to rarer and more specialized species, whereas lower elevations were dominated by generalists. Taxa with elevation restrictions showed significant niche difference.
There is clear seasonal fluctuation, with migratory species such as the pink starling showing up in the winter. Bird communities in lower and mid-elevation zones are negatively impacted by human pressures including tourism, deforestation, and land-use change. By showing how elevation affects species distribution, identifying important species with limited altitudinal ranges, recording seasonal variations, and connecting human-induced changes to biodiversity decrease, the findings support the goals of the study. These results support the necessity of context-based conservation strategies and highlight the ecological vulnerability of semi-arid hill ecosystems. Low altitudes had the lowest diversity indices (Shannon Index: 2.89; Simpson Index: 0.87), whereas middle elevations had the greatest (Shannon Index: 3.61; Simpson Index: 0.94). The mid-zone contains more heterogeneous communities and a more uniform distribution of species. Elevation was significantly correlated with species richness, according to regression analysis (R² = 0.62; p < 0.01).
Table 3: Avian Species Observed in the Harsh-Jeen Region
|
S. N. |
Common Name |
Scientific Name |
IUCN Status |
Elevation Range |
Migratory Status |
Habitat Type |
||
|
1 |
Indian Peafowl |
Pavo cristatus |
Least Concern
|
Low to High
|
Resident |
Scrubland Forest |
||
|
2 |
Rose-ringed Parakeet |
Psittacula krameri
|
Least Concern |
All Zone |
Resident |
Urban, Agricultural |
||
|
3 |
Common Myna |
Acridotheres tristis |
Least Concern |
Mid to High |
Resident |
Urban, Agricultural |
||
|
4 |
Black Drongo |
Dicrurus macocerus |
Least Concern
|
Low to High
|
Resident |
Farmland, Open Areas
|
||
|
5 |
Red-vented Bulbul |
Pycnonotus cafer |
Least Concern |
All Zone |
Resident |
Forest Edge
|
||
|
6 |
Indian Robin
|
Saxicoloides fulicatus |
Least Concern |
Mid to High |
Resident |
Rocky Areas, Grassland |
||
|
7 |
Green Bee-eater |
Merops orientalis |
Least Concern |
Low to Mid |
Resident |
Open Areas |
||
|
8 |
House Sparrow |
Passer domesticus |
Least Concern |
All Zones |
Resident |
Urban, Rural |
||
|
9 |
Common Hoopoe |
Upupa epops |
Least Concern |
Mid |
Resident |
Scrubland Grassland |
||
|
10 |
Rosy Starling |
Pastor roseus |
Least Concern |
Low |
Winter
Migrant |
Agricultural Fields |
||
|
11 |
Ashy Prinia |
Prinia socialis
|
Least Concern |
Low to Mid |
Resident |
Bushland
|
||
|
12 |
Jungle Babbler
|
Turdoides striata
|
Least Concern |
All Zones
|
Resident |
Forest, Village Edges
|
||
|
13 |
Brahminy Starling
|
Sturnia pagodarum
|
Least Concern |
Mid |
Resident |
Grassland, Farmlands |
||
|
14 |
White-throated Kingfisher
|
Halcyon smyrnensis
|
Least Concern |
All Zones
|
Resident |
Dry Deciduous Forest
|
||
|
15 |
Indian Grey Hornbill |
Ocyceros birostriss
|
Least Concern |
Low |
Resident |
Dry Deciduous Forest
|
||
|
16 |
Coppersmith Barbet
|
Psilopogon haemacephalus
|
Least Concern |
Low |
Resident |
Urban Tress |
||
|
17 |
Spotted Dove
|
Spilopelia chinensis
|
Least Concern |
All Zones
|
Resident |
Urban Agriculture |
||
|
18 |
Laughing Dove
|
Spilopelia senegalensis
|
Least Concern |
All Zones
|
Resident |
Farmlands, Scrubland |
||
|
19 |
Shikra
|
Accipiter badius
|
Least Concern |
Low to Mid |
Resident |
Forest, Open Areas
|
||
|
20 |
Indian Roller
|
Coracias benghalensis
|
Least Concern |
All Zones |
Resident |
Open Woodlands
|
||
|
21 |
Black Kite
|
Milvus migrans
|
Least Concern |
All Zones |
Resident |
Urban Scavenging Areas |
||
|
22 |
Eurasian Collared Dove
|
Streptopelia decaocto
|
Least Concern |
All Zones |
Resident |
Urban Semi- Urban
|
||
|
23 |
Rufous Treepie
|
Dendrocitta vagabunda
|
Least Concern |
High |
Resident |
Dry Forests
|
||
|
24 |
Indian Silverbill
|
Euodice malabarica
|
Least Concern |
Low |
Resident |
Grassland, Agricultural
|
||
|
25 |
Greater Coucal
|
Centropus sinensis
|
Least Concern |
Low to Mid |
Resident |
|
||
|
26 |
Tickell’s Blue Flycatcher |
Cyornis tickelliae
|
Least Concern |
Mid |
Resident |
Forested Streams
|
||
|
27 |
Brown Rock Chat
|
Oenanthe fusca
|
Least Concern |
High |
Resident |
Rocky Terrain
|
||
|
28 |
Pied Bushchat
|
Saxicola caprata
|
Least Concern |
Mid to High |
Resident |
Farmlands |
||
|
29 |
Oriental Magpie Robin
|
Copsychus saularis
|
Least Concern |
All Zones |
Resident |
Gardens, Forests
|
||
|
30 |
Common iora
|
Aegithina tiphia
|
Least Concern |
Low to Mid |
Resident |
Forest Edge Scrub |
||
|
31 |
Indian Paradise Flycatcher
|
Terpsiphone paradisi
|
Least Concern |
Mid to High |
Summer Visitor |
Forest Canopy |
||
|
32 |
Bay-backed Shrike
|
Lanius vittatus
|
Least Concern |
Low |
Resident |
Agricultural fields |
||
|
33 |
Long-tailed Shrike
|
Lanius schach
|
Least Concern |
Mid |
Resident |
Open Scrubland |
||
|
34
|
Red-wattled Lapwing
|
Vanellus indicus
|
Least Concern |
Low to Mid |
Resident |
Water Bodies |
||
|
35 |
Little Egret
|
Egretta garzetta
|
Least Concern |
Low |
Resident |
Marshes Wetland |
||
|
36 |
Indian Pond Heron
|
Ardeola grayii
|
Least Concern |
Low |
Resident |
Wetlands Fields |
||
|
37 |
Grey Francolin
|
Francolinus pondicerianus
|
Least Concern |
Low to Mid |
Resident |
Grassland, Agricultural
|
||
|
38 |
Painted Stork
|
Mycteria leucocephala
|
Least Concern |
Low |
Resident |
Wetlands
|
||
|
39 |
Common Kestrel
|
Falco tinnunculus
|
Least Concern |
High |
Winter Visitor |
Rocky Slopes |
||
|
40 |
Crested Serpent Eagle
|
Spilornis cheela
|
Least Concern |
Mid |
Resident |
Woodland, Hills
|
||
|
41 |
Yellow-eyed Babbler
|
Chrysomma sinense
|
Least Concern |
Low |
Resident |
Scrub, Grassland
|
Visual Data Representations
Chart 1: Seasonal Diversity Trends (Shannon Index):
The line graph illustrates seasonal variations in bird diversity (Shannon Index) across the three elevation zones. Bird diversity was consistently highest in the mid-elevation zone, especially during the monsoon and winter seasons. The low and high zones showed more fluctuation, suggesting higher sensitivity to seasonal changes
Chart 2: Species Richness Across Elevation Zones
Figure 1. Seasonal Diversity harsh jeen
Chart 2: Species Richness Across Elevation Zones:
This bar chart displays the total number of bird species recorded across three elevation zones in the HARSH-JEEN hills. Species richness peaked at the mid-elevation zone (500–650 m) with 78 species, followed by the high zone (67 species) and the low zone (61 species). This pattern supports a unimodal distribution, often seen in elevation biodiversity studies.
Figure 2. Species Richness Across Elevation Zones
Chart 3: Land Use Classification by Elevation Zone
This stacked bar chart shows the proportion of land cover types—forest, scrubland, agriculture, and built-up area—across elevation zones. The low zone is heavily influenced by agriculture and built-up areas, while the mid and high zones are dominated by forest and scrubland. This gradient reflects how land-use intensity decreases with elevation, aligning with observed patterns of habitat disturbance.
Figure 3. Land Use Classification by Elevation Zone
Chart 4: Community Perception of Threats
The pie chart summarizes local community responses (n=25) regarding perceived threats to bird populations. Habitat loss was the most cited concern (35%), followed by tourism pressure (25%), forest clearance (20%), and general decline in bird sightings and calls (20%). These perceptions align with observed ecological stressors in the region.
Figure 4. Community Perception of Threats
The varied bird species of the Harsh-Jeen hills is influenced by habitat type and elevation. The significance of this environment is demonstrated by the existence of species that are elevation-restricted and conservation-priority. However, there are significant risks due to growing anthropogenic forces. Elevation-specific conservation initiatives that incorporate environmentally friendly tourist regulations and community involvement are required. The study offers baseline data that are essential for long-term arid hill monitoring of biodiversity and policy development.