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Article

Climate Change and Human Activities, the Significant Dynamic Drivers of Himalayan Goral Distribution (Naemorhedus goral)

1
Department of Ethnobotany, Institute of Botany, Ilia State University, 0162 Tbilisi, Georgia
2
Department of Botany, University of Okara, Okara 56300, Pakistan
3
National Center for Wildlife, Riyadh 11575, Saudi Arabia
4
Department of Botany, Institute of Life Sciences, State Museum of Natural History, 76133 Karlsruhe, Germany
5
Department of Botany, Government Hashmat Ali Islamia Associate College Rawalpindi, Rawalpindi 46300, Pakistan
6
Department of Botany, Pir Mehr Ali Shah Arid Agriculture University Rawalpindi, Rawalpindi 46300, Pakistan
7
School of Public Health, University of California, Berkeley, 2121 Berkeley Way, Berkeley, CA 94704, USA
8
Prince Sultan Bin Abdulaziz International Prize for Water Chair, Prince Sultan Institute for Environmental, Water and Desert Research, King Saud University, Riyadh 11451, Saudi Arabia
9
Department of Agricultural Engineering, College of Food and Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia
10
Plant Production Department, College of Food & Agriculture Sciences, King Saud University, Riyadh 11451, Saudi Arabia
*
Authors to whom correspondence should be addressed.
Biology 2023, 12(4), 610; https://doi.org/10.3390/biology12040610
Submission received: 15 March 2023 / Revised: 14 April 2023 / Accepted: 15 April 2023 / Published: 18 April 2023

Abstract

:

Simple Summary

The objective of our study was to gain a deep understanding about the role of predicted climate change on the range restricted and high-mountain dwelling animal species like the Himalayan goral (HG). To achieve this, we conducted species distribution modeling of the target species under present and predicted future climate change scenarios. Our focus was on identifying the potential suitable microhabitats of the target species using a predictive modeling and maximum entropy algorithm under current climate, and any possible range variation and shift under future climate change scenarios. Annual precipitation and elevation are important factors that affect goral distribution; the elevation between 2000 and 3000 m is thought to be the most suitable for the goral’s habitat. Additionally, a general slight range shift toward northern latitudes and along the higher elevations is observed. Our analysis shows that the suitability of the Himalayan goral’s habitat can change dramatically depending on the forecast. This work might fill the existing knowledge gap about the target species distribution in the study area and predict suitable habitats necessary for species conservation. This study might also be helpful in future planning, management, and sustainable use of available resources, and to mitigate the possible negative effects of climate change in the Himalayan region.

Abstract

The distribution of large ungulates is more often negatively impacted by the changing climate, especially global warming and species with limited distributional zones. While developing conservation action plans for the threatened species such as the Himalayan goral (Naemorhedus goral Hardwicke 1825; a mountain goat that mostly inhabits rocky cliffs), it is imperative to comprehend how future distributions might vary based on predicted climate change. In this work, MaxEnt modeling was employed to assess the habitat suitability of the target species under varying climate scenarios. Such studies have provided highly useful information but to date no such research work has been conducted that considers this endemic animal species of the Himalayas. A total of 81 species presence points, 19 bioclimatic and 3 topographic variables were employed in the species distribution modeling (SDM), and MaxEnt calibration and optimization were performed to select the best candidate model. For predicted climate scenarios, the future data is drawn from SSPs 245 and SSPs 585 of the 2050s and 2070s. Out of total 20 variables, annual precipitation, elevation, precipitation of driest month, slope aspect, minimum temperature of coldest month, slope, precipitation of warmest quarter, and temperature annual range (in order) were detected as the most influential drivers. A high accuracy value (AUC-ROC > 0.9) was observed for all the predicted scenarios. The habitat suitability of the targeted species might expand (about 3.7 to 13%) under all the future climate change scenarios. The same is evident according to local residents as species which are locally considered extinct in most of the area, might be shifting northwards along the elevation gradient away from human settlements. This study recommends additional research is conducted to prevent potential population collapses, and to identify other possible causes of local extinction events. Our findings will aid in formulating conservation plans for the Himalayan goral in a changing climate and serve as a basis for future monitoring of the species.

1. Introduction

The Himalayan ecosystem is highly susceptible to climate change, especially global warming [1]. Global hotspots of biodiversity, with high levels of species diversity and a large number of endemics, are facing the enormous threat of species extinction [2]. A recent report on global biodiversity states that nearly one million species of plants and animals are facing the threat of extinction [3]. According to the latest IUCN Red List, approximately 42,100 species are classified as threatened, making up nearly one-third of all assessed species [4]. In general, endemic species with limited geographical arrays are at higher risk of extinction than those with wide geographic range [5]. The primary causes of species extinction on a global scale are changes in climate, land use, excessive exploitation, poaching, pollution, and invasive alien species [6]. The ongoing threat to global biodiversity posed by these factors is thought to be climate change [7]. The sustained solution to address both climate change and the biodiversity crisis is believed to be the implementation of nature-based solutions that protect natural ecosystems and recover species [8].
When implementing recovery efforts, it is critical to give priority to disturbed landscapes that could enable biodiversity conservation, especially of endemic species which are more vulnerable to extinction [9]. As a result of climate change, it can be challenging for conservation managers to decide where to restore and how to recover when attempting to restore species. Species distribution modeling (SDM), a tool that determines suitable habitats and predicts range shifts under climate change projections, presents an encouraging approach to plan recovery methods for endangered endemic species in regions of high biodiversity (e.g., the Himalaya) [10]. SDM methods have recently been utilized in fields such as invasion biology, restoration ecology, and conservation ecology to forecast hotspots for the protection and cultivation of endemic and threatened taxa [11,12]. The SDM method, based on the niche conservatism theory, predicts the distribution of species along spatio-temporal gradients using a combination of climatic and other environmental variables with data on species distribution [13]. The influence of future climate change on a region of appropriate habitat for a species is frequently predicted using the niche modeling technique known as the MaxEnt (maximum entropy) model [14]. The MaxEnt model can accurately forecast a small number of species distribution ranges, making it ideal for making predictions about some threatened or endemic animals. The first challenge, to determine where to restore, can be addressed by using the projected appropriate locations as potential locations for the vulnerable species’ recovery [15]. The SDM method for identifying suitable sites considering climate only is inadequate for successful species recovery. To overcome this limitation, it is essential to evaluate the biotic and microhabitat conditions at the SDM-determined habitats as well. This will address the second challenge in recovery ecology [16]. Therefore, combining previously largely unrelated areas of research like macro-spatial SDM insights with local-scale ecology could aid in creating effective recovery strategies.
The Himalayan goral (HG) is endemic to the Himalayan Mountains in Asia, including southern Tibet in China, Bhutan, northern India (Himachal Pradesh, Arunachal Pradesh, Jammu and Kashmir, Sikkim, and Uttarakhand), northern Pakistan, Nepal, and possibly western Myanmar [17,18,19]. The subspecies N. goral bedfordi occurs in Himachal Pradesh, Jammu and Kashmir, Uttaranchal, and N. goral in Arunachal Pradesh and Sikkim [17]. Himalayan goral (N. goral bedfordi) is listed as Near Threatened [20]. Furthermore, fossil records indicate that the current Southeast Asian caprine populations represent relict groups that were once more widespread during the Pleistocene era but became limited to highlands and high-altitude mountain ranges during the Holocene interglacial period. This suggests that these caprines were abundant in tropical lowlands and may have exhibited habitat partitioning in past coexistence areas, given their close genetic relatedness [21]. High potential sites for goral distribution in Jammu and Kashmir along the Pirpanjal and Ka-zi-Nag Range comprise Shamshabari, Kazinag National Park, Limber Wildlife Sanctuary, Lachipora Wildlife Sanctuary, Naganari Conservation Reserve, Ta-takuti-Kalamuund Wildlife Sanctuary, and Khara Gali Conservation Reserve. [17,18].
The term “Himalaya” means “the abode of snow” in Sanskrit. The Himalayas were created around 50 million years ago as a result of the Indian and Eurasian plates colliding, according to the continental drift theory [22]. As a result of the collision between India and Eurasia, a complex geological wedge has been formed, where three tectonic domains have been added to the structure in a north-to-south direction. These domains are known as the High Himalaya, the Lesser Himalaya, and the Sub-Himalaya [23]. The Himalayas is warming at a relatively faster rate (0.06 °C/year) compared to the rest of the globe [24], which raises the possibility of species extinction in the area. The region may become a hotspot for species losses as a result of human and climate-related risks to wildlife. It is predicted that the Himalayas’ rapidly changing climate will increase the extinction risks in the near future, especially for endemic and threatened species. As a result, it is necessary to integrate threats caused by climate change into policies for conserving nature and species recovery practices.
This study used MaxEnt modeling to identify the Himalayan goral’s current appropriate habitats over the entire Himalayan range and estimate how their range might change in relation to various predicted future climate change scenarios. To address the recovery issues, this study asks the following questions: 1. Where are the suitable microhabitats for the Himalayan goral in the Himalayas under current and future climate change scenarios, and what are the leading environmental variables? 2. How will the predicted distribution range of the species respond under different future climate change scenarios? 3. How can the SDM predictions be used to guide the recovery efforts for Himalayan goral in the study area?

2. Materials and Methods

2.1. Study Area

The Himalayas, meaning “Abode of Snow,” is a relatively young mountain range separating the Indo-Gangetic Plain and the Tibetan Plateau. This range spans nearly 2400 km in length from Afghanistan in the west to Burma in the east (27–36° N latitude and 72-91° E longitude), it connects the Near East and Central Asia with East Asia (Figure 1). The range is shared by five countries: Nepal, India, China (Tibet), Bhutan, and Pakistan, with most of it being in the first three.

2.2. Species Presence Data

To gather the species presence data, Himalayan goral potential occurrence sites in the study area were identified using field surveys, literature, and the GBIF (Global Biodiversity Information Facility) database. From the GBIF and published data, records of species distribution from 1864 to 2019 were chosen, and duplicate records were eliminated. To avoid the spatial pseudo-replication, only GPS (global positioning system) locations with an accuracy of 15 m were selected and filtered to keep one presence point within each of 5 km2 pixel based on raster data resolution (i.e., 2.5 arc-min).
We conducted field surveys between the years 2015 and 2021 to record the Himalayan goral presence. The goral was observed with the aid of binoculars (8 × 40) and a spotting scope (15 × 45) from trails and vantage points across the potential habitat. Sightings and signs were recorded with the habitat features distance to the nearest cliff and slope attributes of ruggedness for every sighting. Locations and elevation were recorded using a handheld GPS. A questionnaire survey was prepared to interview knowledgeable local persons and various department staff about their knowledge of the possible presence of goral in the area. The observers’ knowledge was assessed through one to one interaction and by discussing the features of goral. A total of 81 distinct location points of the targeted species were used to build the SDM.

2.3. Environmental Data Collection and Variable Selection

A total of 19 bioclimatic variables (resolution: 2.5 arc-min) and elevation data (resolution 30 arc-s) was obtained from the WorlClim (ver. 2.1) (www.worldclim.org, accessed on 15 June 2022). Elevation data was further processed in ArcGIS to generate the slope and aspect variables. Additionally, the topographic data was resampled to bioclimatic data resolution. For future simulations, two shared socio-economic pathways (SSPs) including SSPs 245 and SSPs 585 of two time spans including 2041–2060 = 2050s, and 2061–2080 = 2070s of Coupled Model Intercomparison Project, Phase 6 (CMIP6) and belonging to Global Climate Model of BCC-CSM2-MR (resolution: 2.5 arc-min) were downloaded and used.
The distribution of Himalayan goral is influenced by various factors including temperature, precipitation, geographical barriers, geological formations, and other biological variables [25]. Our model used a total of 19 bioclimatic and three biophysical variables (elevation, slope, and aspect) to assess the environmental factors impacting species distribution.
To ensure independence and eliminate spatially correlated data points, this study employed the following two-step procedure. First, a preliminary model (with default setting) was run to assess the variables contribution. A threshold value of >1% was used to screen the variables. In the second step, the remaining variables (above contribution threshold) were analyzed for a pairwise Pearson’s correlation (r). A threshold value (r ≥ ±0.8) was used to further reduce the number of variables. Any two variables with an r value above the selected threshold were targeted, and those contributing less were omitted [26,27,28].

2.4. Preliminary Varaibles Processing

The threshold application and Pearson’s correlation coefficient resulted in a total of eight crucial bioclimatic and topographic variables. These include minimum temperature of coldest month, annual precipitation, precipitation of warmest quarter, annual temperature range, precipitation of driest month, aspect, slope, and elevation [29]. The pairwise correlation of the finally selected variables is also presented (Figure 2).

2.5. Model Calibration and Optimization

MaxEnt prediction model calibration and optimization is crucial in SDM to select the best candidate model. Selecting different regularization multiplier (RM) values and feature classes (FC) are generally required to tune the model for better prediction reliability. The optimal MaxEnt model settings were identified based on threshold-dependent (i.e., omission rate) evaluation metrics, in order to prevent overfitting and improve model transferability. For this, multiple combinations of both RM values (a total of eight different values with range: 1–4, and interval: 0.5) and six FCs (L, LQ, H, LQH, LQHP, and LQHPT where L = Linear, Q = Quadratic, H = Hinge, P = Product, T = Threshold) were targeted [30]. The ENMEval package in R was used to build the bias file using occurrence and environmental data to be used in the model.
The data for this study was analyzed using MaxEnt 3.4.4. to forecast the optimal habitats for Himalayan goral in the study region [31]. The MaxEnt model, based on ecological niche theory, predicts the possible distribution of a target species within a research area using presence data information [32]. MaxEnt software uses species presence data to identify the most suitable habitats for the target species with high accuracy [31] and it is one of the most advanced and promising SDM techniques [33,34]. MaxEnt has overtaken other approaches used for the aforementioned reasons due to its superior prediction accuracy [35,36].
We applied MaxEnt, a highly accurate machine-learning species distribution modeling approach, to model the connection between wildlife distributions and environmental conditions [36], to create models of the interactions between the species occurrences and climatic factors. The other MaxEnt settings for better prediction accuracy and model performance include use of 10th percentile presence probability of the species, 10-fold cross-validation method, complementary log-log (clog-log) output format, 10,000 background points, 10 replicate runs, 500 iterations, response curves development, and testing of jackknife importance in all the final optimized SDMs.

2.6. Model Evaluation and Preditions Reclassification

The evaluation of the optimized SDMs was assessed using area under curve (AUC) of the receiver-operator characteristic (ROC) curve values. The AUC-ROC value of >0.9 was considered an excellent model for predictive performance [31,33,37,38]. The AUC score evaluates the model’s capacity to discriminate between changes in species distribution under potential future climatic scenarios and reflects how well the model fits the test data [31,37]. AUC values closer to 1.0 indicate that the model performs better than chance, whilst 0.5 indicates that the model performs no better than chance [37]. The averaged MaxEnt prediction output for the possible existence of Himalayan goral in the study area varied from 0–1. The modeled outputs were classified into a total of four habitat suitability levels: 1. 0–0.2 not suitable habitat; 2. 0.21–0.5 low suitability habitat; 3. 0.51–0.8 moderately suitable habitat, and 4. 0.81–1 highly suitable habitat [39,40,41,42].

3. Results

3.1. Model Evaluation

MaxEnt generated outputs for 10 replications, which were then averaged into a single model prediction, along with response curves and the AUC graph. The average model was used to evaluate prospective migration paths and make suitability assumptions. Our findings suggest that the use of LQH as FCs in combination with an RM value of 1.5 produced the optimal candidate model with an AUC score of 0.965. The projected range of the Himalayan goral in the whole Himalaya region received a predictive habitat suitability score ranging from 0 to 0.96. The AUC value of the MaxEnt model can be used directly as a standard for model prediction performance because it can calculate the ROC curve and draw it on its own. The expected outcomes of this study’s ROC curve are displayed in Figure 3. According to the findings of the curve analysis, the model’s average AUC value was 0.965, which was much higher than the AUC value of the random prediction model (0.5), indicating that the predicted outcomes had a better degree of accuracy. This meant that the model’s anticipated distribution area and the species’ actual distribution area were a good fit.

3.2. Environmental Variables Responsible for the Distribution

The variables with a higher contribution percentage for habitat suitability of Himalayan goral includes annual precipitation, elevation, precipitation of driest month, aspect, and minimum temperature of coldest month. The variables with relatively low contribution in the SDMs of Himalayan goral included slope, precipitation of warmest quarter, and temperature annual range (Table 1). The findings revealed that the way the chosen variables characterize Himalayan goral current distribution was excellent. The jackknife test showed that the MaxEnt model’s contributions to the distribution of Himalayan goral were 38.2% and 32.2% for the annual precipitation (Bio12) and the elevation, respectively (Figure 4). We undertook a single study to show the influence of Bio12 and elevation as a single factor because of their highest contribution rates. The chance of Himalayan goral presence increased initially and then declined as annual precipitation increased (Figure 5). The probability was greater than 0.6 when annual precipitation was between the ranges of 700–1000 mm, indicating a very appropriate location, whereas the chance of presence peaked at around 1200 mm, or about 0.7. The elevation for highly suitable habitats ranged from 2000–3000 m (Figure 5).

3.3. Current Distribution

The Himalayan range encompasses seven Asian countries, including India. It occupies an area of (about) 2500 km2 over 11 states and Jammu and Kashmir (J&K) in India (Figure 1). The current suitable locations of Himalayan goral were obtained through a species distribution model that predicted their occurrence (Figure 6). The Himalayan goral is thought to reside in the Himalayan region that stretches from Nepal to northwest India, crossing via the J&K region to reach Afghanistan. However, the necessary habitats are not evenly distributed throughout the upper Himalayas. We found that high suitable and medium suitable habitats are spread in patches throughout the Himalayas from north-eastern Afghanistan to central Nepal. Along the Pakistan-Afghanistan border, in the Uttarakhand, Kashmir region, and in the Annapurna region are continuous stripes of highly suitable habitats.

3.4. Potential Habitat Suitability under Future Climate Change Scenarios

When future climate change possibilities were considered collectively, we found that existing most suitable habitat is disappearing and shifting northward as well as along the elevation gradient. In future, in all four SSPs scenarios of the 2050s and 2070s, the predicted suitable habitat might shift northward in Jammu and Kashmir, Pakistan, Uttarakhand, and Nepal, resulting in an uninterrupted distribution of extremely appropriate locations in the north section of J&K territory and their adjacent areas (Figure 7). In four scenarios, however, the availability of suitable habitat is limited. The majority of the appropriate location would be accessible in west Himachal Pradesh and Uttarakhand and moreover their surrounding region in Tibet beside the boundary of the three nations by the year 2050 (SSPs 245 and SSPs 585). The majority of the habitat would vanish between the Nepal area and the Pak-Afghan border in 2050, according to the SSPs 346 scenario, although there would be small strips of appropriate habitat in Himachal between the Kashmir region and Uttarakhand. By 2050, the Kashmir region, the Pak-Afghan border, and the Annapurna region might be devoid of suitable habitat for the Himalayan goral according to the SSPs 245 and SSPs 585 scenarios.
All the predicted highly suitable habitats near the Pakistan-Afghanistan border, Kashmir, and Himachal might be lost by 2070s under all the four considered future climate change scenarios. The Himalayan regions in the west of Uttarakhand, including the Indian, Pakistani, and Afghan Himalayas, might face the disappearance of all the existing or current suitable and highly suitable habitats in the 2050s and 2070s under scenarios SSPs 245 and SPPs 585. It is anticipated that Pakistan, Kashmir, and central Nepal might have only marginally suitable locations in the Pak-Afghan border region between 2050 and 2070.
By 2050, the habitat for Himalayan goral under the SSPs 585 scenario would have expanded more than SSPs 245 and this habitat is anticipated to be dispersed densely over west Nepal, Uttarakhand, and their connected territories in Tibet (Figure 7). By 2070, the habitat would have a similar pattern in the SSPs 245 and SSPs 585 scenarios. However, in SSPs 585 scenarios, the habitat of Himalayan goral would be enlarged in Uttarakhand, west Nepal, and their surrounding territories in Tibet.

4. Discussion

Multiple improvements in GIS technology especially during the last two decades have enabled the gathering of diverse spatial and temporal datasets, leading to better understanding of species distribution and the impact of environmental factors at multiple scales [43]. The current study is the first comprehensive analysis of the distribution, habitat appropriateness, and hotspot predictions of the Himalayan goral. According to habitat suitability classes selected in this study (Table 2), least suitable (p 0.21–0.4), moderately suitable (p 0.41–0.6), and highly suitable (p 0.61–0.8) areas for the Himalayan goral are predicted to shrink, whereas very high suitability areas (p 0.81–1.0) are predicted to expand remarkably in future. This possible shrinkage in some parts might be due to the increasing rate of existing habitat degradation based on accelerated construction, urbanization, and deforestation in the study area. Our model demonstrated exceptional performance, with strong predictive ability and highly significant predictions, as evidenced by an AUC value greater than 0.9 [44,45,46]. Our model’s AUC value for the current climate modeling was 0.965, indicating that it accurately and thoroughly characterized the Himalayan goral habitat, and significantly distinguished between the possible presence and absence of the targeted species in the Himalayan geographic range. The most recent assessment of habitat appropriateness was perfectly in line with the analysis’ utilization of the available occurrence records. Because annual precipitation (BIO 12) and minimum temperature of the coldest month (BIO 6) were two of the top bioclimate variables contributors to the model, precipitation was the most influential variable on the distribution of Himalayan goral. This is consistent with [47], who stated that annual precipitation (BIO 12) was the main factor influencing the spread of Himalayan goral found in Pakistan. Similarly, elevation was the other key characteristic to predict its habitat. The MaxEnt model results predicted that the most optimal elevation range for the Himalayan goral varies from 2000 to 3000 m above sea level (ASL). This is consistent with what is known about the species, as it is typically found at extreme elevations ranging from 1000 to 4000 m ASL. Within this elevation range, the goral may prefer areas with a mix of vegetation types, including open grasslands, shrublands, and forests. The availability of water sources, such as streams or springs, may also be an important factor in habitat selection, and directly depend on precipitation type, pattern, and amount in the study area. Many researchers reported a similar altitude range as the ideal habitat for goral in India and other native neighboring regions [43,48,49,50].
Therefore, elevation is the key factor influencing the distribution of the Himalayan goral. The SDM results in this study are aligned accordingly, and elevation is detected as the second-highest contributor, which agrees with [43], who identified altitude as one of the key elements of Himalayan goral habitat that sets it apart from other ungulates. However, the elevation range between 2000 and 3000 m ASL is regarded as the most favorable as an appropriate microhabitat in the study area. However, the local residents suggested that the Himalayan goral is probably shifting further upward along the elevation and trying to avoid the growing heat and anthropogenic disturbances. Our research confirms [43] findings that the preferred habitat for the Himalayan goral in Pakistan is the upper mid-hill to high-mountain region (more than 2000 m ASL). Under both SSPs 245 and 585 scenarios, it is projected that the Himalayan goral habitat will experience an overlap in the future, with a significant proportion of the habitat shifting. The model also showed that any future shift in habitat along the elevation gradient might mostly lean longitudinally rather than latitudinally in the study area. This demonstrates that the Himalayan goral is sedentary by nature and stays within a predetermined home range throughout the year.
In order to create efficient conservation strategies, it is essential to comprehend how animals react to climate change [51,52]. The direct effects of climate change on the ecosystems of diverse species have already been highlighted in numerous studies [51,53,54]. The current study presents the first extensive evaluation of how the distribution of Himalayan goral may vary under climate change scenarios. We used the MaxEnt modeling approach to cover the entire Himalayan region where the species is known to exist, and predicted both the current and future possible distribution using the MaxEnt modeling technique and a range of greenhouse gas emission scenarios over a number of time periods. Under SSPs 245, the currently suitable habitats decreased and shifted to eastern Himalayan regions in the years 2050 and 2070, while both the range and the suitable habitat decreased under SSPs 245 and SSPs 585 scenarios (2050s and 2070s). The distribution of large mammals is affected by climate change, but not uniformly across species. The expected habitat fluctuation during climate change differs depending on the species. The findings of [55] reveal that African mammals respond differently to scenarios of global climate change, with some species losing nearly all of their viable habitats while others remained steady or even gained new habitats. Our findings are consistent with these studies [56,57].
Our findings demonstrated that the regional distribution of Himalayan goral would decrease under the predicted climatic circumstances for the years 2050 and 2070 under the two tested SSPs (245 and 585). The simulations showed that when this species disappears from human view, the habitat range and core habitats might shift in future. The environmental envelope (precipitation and temperature) of the Himalayan goral will become less conducive to its existence, which might be the cause of the range shift. The Himalayan goral lives on isolated patches in the study area, making them more vulnerable to climate change since species with small ecological niches are more susceptible to climate change than species with broader ecological niches [58,59].
Despite their undeniable significance in defining the geographic range of many species, it is interesting to note that climatic influences are not the only ones causing species to disperse throughout any land area [14]. To forecast a more accurate image of the spatial distribution of the species, other ecological aspects such as ecological interactions, dispersal pattern and capability, habitat preference, resource distribution, and availability merit careful investigation and improved integration within SDMs [36]. The inability to completely incorporate the species ecology ideas into the modeling process due to incomplete data has added some constraints to this work. Sample size, sampling bias, the geographical resolution of the predictors, including their selections, and multi-collinearity issues are additional elements that affect the SDM’s limitations and uncertainties. These issues should be carefully considered during the modeling process [60,61]. However, MaxEnt is considered as the most appropriate tool due to its outstanding predictive strength and ability to function admirably with tiny sample sizes. Although this study tried to address the multi-collinearity problems (by removing the variables that are strongly correlated) and background sampling bias (by just using background samples from the region of occurrence records), we recognize that there may still be some uncertainty in the results as biotic interactions and dispersal capacity were not targeted. The estimated potential distribution maps of the species’ suitable habitats should be further refined in future by including the physiologically pertinent parameters in the modeling process. The predictions presented in this study for the region might warrant some serious consideration for species conservation in light of climate change, especially global warming.
The current study is the first to describe the link between ecological parameters and habitat viability, anticipate changes in habitat suitability due to predicted climate change, and model the Himalayan goral in its distributional range. The findings are in line with earlier research on climate change in the same ecosystems, and demonstrate that the habitat appropriateness of the Himalayan goral is substantially related to climate in the area [62,63,64]. With a lack of research on Himalayan goral distribution in the study area, the findings of this study strongly support additional investigation. For conservation strategies and plans, it is strongly advised to announce the expected suitable areas as nature reserves to house more diversity with few risks in both the existing and anticipated future climatic conditions.
The extinction of local species is considered a leading cause of alterations in the structure and function of the ecosystem in any area [65,66,67,68]. Our research area includes multiple biodiversity hotspots, contains a high percentage of vulnerable species, and has seen an increase in recent years in the risk of extinction, mostly as a result of habitat degradation and illegal hunting [69,70,71,72]. We have assessed and mapped the currently acceptable habitat for this species as well as projections for it under scenarios of a warming climate and changing land use. Our study also offers opportunities for protecting numerous other species that share its habitat. To help reduce biodiversity loss due to habitat degradation and loss, for instance, our suitable location map and forecasting could be utilized to pinpoint crucial habitat areas requiring instant conservation efforts. Additionally, our high-resolution maps could assist park managers and conservationists in identifying and prioritizing conservation efforts for crucial habitats, focusing on preserving threatened remnant patches and critical connecting habitats that are forecasted to vanish in the future.
Understanding the influence of climate change and human threats on Himalayan goral distribution is crucial for managing such species and mitigating potential threats. Our research provides a preliminary evaluation of the effect of climate change on the distribution of HG in its primary habitats in the Himalayan region. This assessment could aid in future analyses of HG distribution across its entire range in the Himalayas and be helpful in creating any management strategies for wildlife conservation in the face of climate change.

5. Conclusions

The current study is the first to identify Himalayan goral (HG) habitat suitability variations under multiple future climate change scenarios in its native range using the MaxEnt modeling tool. The two main environmental factors, Bio12 and elevation, were found to have major effects on HG distribution. Overall, the suitable habitat might shrink under the predicted 2050s and 2070s future climate change scenarios. The current modeling framework demonstrated habitat suitability under both the present climate and future climate change predictions based on various possible greenhouse gas emission scenarios. This study might serve as a baseline work and be useful in developing and putting into practice conservation strategies for the HG in order to lessen the effects of climate change and human disturbance. This study suggests that such an approach might make it possible to undertake more habitat assessments in conditions where semi-structured field surveys are feasible but adequate funding and statistical know-how are not immediately available.

Author Contributions

Conceptualization, S.M.H.; methodology, S.M.H., A.M.K., M.W. and R.A.; software, M.W., A.M.K. and S.M.H.; validation, S.M.H., R.A., R.W.B. and F.A.; formal analysis, S.M.H. and M.W.; investigation, S.M.H.; resources, R.C., H.O.E., A.A. and A.Z.D.; data curation, M.W. and F.A.; writing—original draft preparation, S.M.H., A.M.K., R.A., R.C., H.O.E., A.A., A.Z.D. and M.W.; writing—review and editing, M.W., A.M.K., R.W.B. and F.A.; visualization, R.W.B.; supervision, S.M.H.; project administration, S.M.H.; funding acquisition, H.O.E. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Deanship of Scientific Research, King Saud University through the Vice Deanship of Scientific Research Chairs; Research Chair of Prince Sultan Bin Abdulaziz International Prize for Water.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data are available within this publication.

Acknowledgments

The authors extend their appreciation to the Deanship of Scientific Research, King Saud University for funding through the Vice Deanship of Scientific Research Chairs; Research Chair of Prince Sultan Bin Abdulaziz International Prize for Water.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Jamwal, P.S.; Di Febbraro, M.; Carranza, M.L.; Savage, M.; Loy, A. Global change on the roof of the world: Vulnerability of Himalayan otter species to land use and climate alterations. Div. Distrib. 2022, 28, 1635–1649. [Google Scholar] [CrossRef]
  2. Negi, G.C.S.; Rawal, R.S. Himalayan biodiversity in the face of climate change. In Tropical Ecosystems: Structure, Functions and Challenges in the Face of Global Change; Springer: Singapore, 2019; pp. 263–277. [Google Scholar]
  3. Díaz, S.; Malhi, Y. Biodiversity: Concepts, patterns, trends, and perspectives. Annu. Rev. Env. Resour. 2022, 47, 31–63. [Google Scholar] [CrossRef]
  4. IUCN. The IUCN Red List of Threatened Species. Version 2022-2. Available online: https://www.iucnredlist.org/ (accessed on 10 December 2022).
  5. Cruz, C.; Santulli-Sanzo, G.; Ceballos, G. Global patterns of raptor distribution and protected areas optimal selection to reduce the extinction crises. Proc. Natl. Acad. Sci. USA 2021, 118, e2018203118. [Google Scholar] [CrossRef] [PubMed]
  6. Caro, T.; Rowe, Z.; Berger, J.; Wholey, P.; Dobson, A. An inconvenient misconception: Climate change is not the principal driver of biodiversity loss. Conserv. Lett 2022, 15, e12868. [Google Scholar] [CrossRef]
  7. Manes, S.; Costello, M.J.; Beckett, H.; Debnath, A.; Devenish-Nelson, E.; Grey, K.A.; Jenkins, R.; Khan, T.M.; Kiessling, W.; Krause, C.; et al. Endemism increases species’ climate change risk in areas of global biodiversity importance. Biol. Conserv. 2021, 257, 109070. [Google Scholar] [CrossRef]
  8. Seddon, N.; Smith, A.; Smith, P.; Key, I.; Chausson, A.; Girardin, C.; House, J.; Srivastava, S.; Turner, B. Getting the message right on nature-based solutions to climate change. Glob. Change Biol. Bioenergy 2021, 27, 1518–1546. [Google Scholar] [CrossRef]
  9. Zhang, Y.; Tariq, A.; Hughes, A.C.; Hong, D.; Wei, F.; Sun, H.; Sardans, J.; Peñuelas, J.; Perry, G.; Qiao, J.; et al. Challenges and solutions to biodiversity conservation in arid lands. Sci. Total Environ. 2022, 857, 159695. [Google Scholar] [CrossRef]
  10. Frans, V.F.; Augé, A.A.; Fyfe, J.; Zhang, Y.; McNally, N.; Edelhoff, H.; Balkenhol, N.; Engler, J.O. Integrated SDM database: Enhancing the relevance and utility of species distribution models in conservation management. Methods Ecol. Evol. 2022, 13, 243–261. [Google Scholar] [CrossRef]
  11. Hernandez, J.O.; Buot Jr, I.E.; Park, B.B. Prioritizing choices in the conservation of flora and fauna: Research trends and methodological approaches. Land 2022, 11, 1645. [Google Scholar] [CrossRef]
  12. Curd, A.; Chevalier, M.; Vasquez, M.; Boyé, A.; Firth, L.B.; Marzloff, M.P.; Bricheno, L.M.; Burrows, M.T.; Bush, L.E.; Cordier, C.; et al. Applying landscape metrics to species distribution model predictions to characterize internal range structure and associated changes. Glob. Change Biol. Bioenergy 2023, 29, 631–647. [Google Scholar] [CrossRef]
  13. Arenas-Castro, S.; Regos, A.; Martins, I.; Honrado, J.; Alonso, J. Effects of input data sources on species distribution model predictions across species with different distributional ranges. J. Biogeogr. 2022, 49, 1299–1312. [Google Scholar] [CrossRef]
  14. Arshad, F.; Waheed, M.; Fatima, K.; Harun, N.; Iqbal, M.; Fatima, K.; Umbreen, S. Predicting the suitable current and future potential distribution of the native endangered tree Tecomella undulata (Sm.) Seem. in Pakistan. Sustainability 2022, 14, 7215. [Google Scholar] [CrossRef]
  15. Dhyani, S.; Singh, S.; Kadaverugu, R.; Pujari, P.; Verma, P. Habitat suitability modelling and nature-based solutions: An efficient combination to realise the targets of Bonn challenge and SDGs in South Asia. In Nature-Based Solutions for Resilient Ecosystems and Societies; Springer: Berlin/Heidelberg, Germany, 2020; pp. 347–364. [Google Scholar]
  16. Fedriani, J.M.; Ayllón, D.; Wiegand, T.; Grimm, V. Intertwined effects of defaunation, increased tree mortality and density compensation on seed dispersal. Ecography 2020, 43, 1352–1363. [Google Scholar] [CrossRef]
  17. Duckworth, J.W.; MacKinnon, J. Naemorhedus goral . In The IUCN Red List of Threatened Species 2008; IUCN: Gland, Switzerland, 2008. [Google Scholar]
  18. Abbas, F.; Ruckstuhl, K.E.; Mian, A.; Akhtar, T.; Rooney, T.P. Distribution, population size, and structure of Himalayan grey goral Naemorhedus goral bedfordi (Cetartiodactyla: Bovidae) in Pakistan. Mammalia 2012, 76, 143–147. [Google Scholar]
  19. Sathyakumar, S. Species of the greater Himalaya. In ENVIS Bulletin: Wildlife and Protected Areas; Sathyakumar, S., Ed.; Wildlife Institute of India: Dehradun, India, 2002; pp. 44–49. [Google Scholar]
  20. Cooke, S.J. Biotelemetry and biologging in endangered species research and animal conservation: Relevance to regional, national, and IUCN Red List threat assessments. Endanger. Species Res. 2008, 4, 165–185. [Google Scholar] [CrossRef]
  21. Suraprasit, K.; Jaeger, J.J.; Shoocongdej, R.; Chaimanee, Y.; Wattanapituksakul, A.; Bocherens, H. Long-term isotope evidence on the diet and habitat breadth of Pleistocene to Holocene caprines in Thailand: Implications for the extirpation and conservation of Himalayan gorals. Front. Ecol. Evol. 2020, 8, 67. [Google Scholar] [CrossRef]
  22. Chatterjee, S.; Goswami, A.; Scotese, C.R. The longest voyage: Tectonic, magmatic, and paleoclimatic evolution of the Indian plate during its northward flight from Gondwana to Asia. Gondwana Res. 2013, 23, 238–267. [Google Scholar] [CrossRef]
  23. Yin, A.; Harrison, T.M. Geologic evolution of the Himalayan-Tibetan orogen. Annu. Rev. Earth Planet. Sci. 2000, 28, 211–280. [Google Scholar] [CrossRef]
  24. Hassan, T.; Hamid, M.; Wani, S.A.; Malik, A.H.; Waza, S.A.; Khuroo, A.A. Substantial shifts in flowering phenology of Sternbergia vernalis in the Himalaya: Supplementing decadal field records with historical and experimental evidences. Sci. Total Environ. 2021, 795, 148811. [Google Scholar] [CrossRef]
  25. Gao, X.; Liu, J.; Huang, Z. The impact of climate change on the distribution of rare and endangered tree Firmiana kwangsiensis using the Maxent modeling. Ecol. Evol. 2022, 12, e9165. [Google Scholar] [CrossRef]
  26. Bosso, L.; Di Febbraro, M.; Cristinzio, G.; Zoina, A.; Russo, D. Shedding light on the effects of climate change on the potential distribution of Xylella fastidiosa in the Mediterranean Basin. Biol. Invasions 2016, 18, 1759–1768. [Google Scholar] [CrossRef]
  27. Khattak, R.H.; Teng, L.; Ahmad, S.; Bari, F.; Rehman, E.U.; Shah, A.A.; Liu, Z. In pursuit of new spaces for threatened mammals: Assessing habitat suitability for Kashmir Markhor (Capra falconeri cashmeriensis) in the Hindukush Range. Sustainability 2022, 14, 1544. [Google Scholar] [CrossRef]
  28. Hijmans, R.J.; Cameron, S.E.; Parra, J.L.; Jones, P.G.; Jarvis, A. Very high-resolution interpolated climate surfaces for global land areas. Int. J. Climatol 2005, 25, 1965–1978. [Google Scholar] [CrossRef]
  29. Graham, M.H. Confronting multicollinearity in ecological multiple regression. Ecology 2003, 84, 2809–2815. [Google Scholar] [CrossRef]
  30. Taylor, K.E.; Stouffer, R.J.; Meehl, G.A. An overview of CMIP5 and the experiment design. Bull. Am. Meteorol. Soc. 2012, 93, 485–498. [Google Scholar] [CrossRef]
  31. Phillips, S.J.; Anderson, R.P.; Schapire, R.E. Maximum entropy modeling of species geographic distributions. Ecol. Model. 2006, 190, 231–259. [Google Scholar] [CrossRef]
  32. Bai, D.-F.; Chen, P.-J.; Atzeni, L.; Cering, L.; Li, Q.; Shi, K. Assessment of habitat Suitability of the Snow Leopard (Panthera uncia) in Qomolangma National Nature Reserve Based on MaxEnt Modeling. Zool. Res. 2018, 39, 373. [Google Scholar]
  33. Fourcade, Y.; Engler, J.O.; Rödder, D.; Secondi, J. Mapping species distributions with MAXENT using a geographically biased sample of presence data: A Performance Assessment of Methods for Correcting Sampling Bias. PLoS ONE 2014, 9, e97122. [Google Scholar] [CrossRef]
  34. Merow, C.; Smith, M.J.; Silander, J.A., Jr. A practical guide to MaxEnt for modeling species’ distributions: What it does, and why inputs and settings matter. Ecography 2013, 36, 1058–1069. [Google Scholar] [CrossRef]
  35. Summers, D.M.; Bryan, B.A.; Crossman, N.D.; Meyer, W.S. Species vulnerability to climate change: Impacts on spatial conservation priorities and species representation. Glob. Change Biol. 2012, 18, 2335–2348. [Google Scholar] [CrossRef]
  36. Elith, J.H.; Graham, C.P.; Anderson, R.; Dudík, M.; Ferrier, S.; Guisan, A.J.; Hijmans, R.; Huettmann, F.R.; Leathwick, J.; Lehmann, A. Novel methods improve prediction of species’ distributions from occurrence data. Ecography 2006, 29, 129–151. [Google Scholar] [CrossRef]
  37. Elith, J.; Phillips, S.J.; Hastie, T.; Dudík, M.; Chee, Y.E.; Yates, C.J. A statistical explanation of MaxEnt for ecologists. Divers. Distrib. 2011, 17, 43–57. [Google Scholar] [CrossRef]
  38. Phillips, S.J.; Dudík, M.; Elith, J.; Graham, C.H.; Lehmann, A.; Leathwick, J.; Ferrier, S. Sample selection bias and presence-only distribution models: Implications for background and pseudo-absence data. Ecol. Appl. 2009, 19, 181–197. [Google Scholar] [CrossRef]
  39. Deb, J.C.; Forbes, G.; MacLean, D.A. Modelling the spatial distribution of selected North American woodland mammals under future climate scenarios. Mamm. Rev. 2020, 50, 440–452. [Google Scholar] [CrossRef]
  40. Yang, X.; Kushwaha, S.; Saran, S.; Xu, J.; Roy, P. Maxent modeling for predicting the potential distribution of medicinal plant, Justicia adhatoda L. in Lesser Himalayan foothills. Ecol. Eng. 2013, 51, 83–87. [Google Scholar] [CrossRef]
  41. Vilà, M.; Gassó, N.; Thuiller, W.; Pino, J. Potential distribution range of invasive plant species in Spain. NeoBiota 2012, 12, 25–40. [Google Scholar] [CrossRef]
  42. Zhao, D.; He, H.; Wang, W.; Wang, L.; Du, H.; Liu, K.; Zong, S. Predicting wetland distribution changes under climate change and human activities in a Mid- and High-Latitude Region. Sustainability 2018, 10, 863. [Google Scholar] [CrossRef]
  43. Hirzel, A.H.; Le Lay, G. Habitat Suitability Modelling and Niche Theory. J. Appl. Ecol. 2008, 45, 1372–1381. [Google Scholar] [CrossRef]
  44. Smeraldo, S.; Di Febbraro, M.; Ćirović, D.; Bosso, L.; Trbojević, I.; Russo, D. Species distribution models as a tool to predict range expansion after reintroduction: A case study on Eurasian beavers (Castor fiber). J. Nat. Conserv. 2017, 37, 12–20. [Google Scholar] [CrossRef]
  45. Wogan, G.O. Life history traits and niche instability impact accuracy and temporal transferability for historically calibrated distribution models of North American birds. PLoS ONE 2016, 11, e0151024. [Google Scholar] [CrossRef]
  46. Domíguez-Vega, H.; Monroy-Vilchis, O.; Balderas-Valdivia, C.J.; Gienger, C.M.; Ariano-Sánchez, D. Predicting the potential distribution of the beaded lizard and identification of priority areas for conservation. J. Nat. Conserv. 2012, 20, 247–253. [Google Scholar] [CrossRef]
  47. Ahmad, S.; Yang, L.; Khan, T.U.; Wanghe, K.; Li, M.; Luan, X. Using an ensemble modelling approach to predict the potential distribution of Himalayan gray goral (Naemorhedus goral bedfordi) in Pakistan. Glob. Ecol. Conserv. 2020, 21, e00845. [Google Scholar] [CrossRef]
  48. Thapa, A.; Thapa, S.; Poudel, B.S. Habitat and distribution of Goral (Naemorhedus goral) in Mahabharat Goral Wildlife Conservation Area, Nawalparasi, Western Nepal. Nepal J. For. 2011, 14, 1. [Google Scholar]
  49. Cavallini, P. Status of goral (Naemorhaedus goral) in Himachal Pradesh, India. Caprinae News 1990, 5, 4–6. [Google Scholar]
  50. Acharya, D.; Aryal, B.; Joshi, S. Locally declared Goral Conservation Area. Conserv. Watch-Nepal. News 2008, 1, 1. [Google Scholar]
  51. Quintero, I.; Wiens, J.J. Rates of projected climate change dramatically exceed past rates of climatic niche evolution among vertebrate species. Ecol. Lett. 2013, 16, 1095–1103. [Google Scholar] [CrossRef]
  52. Warren, D.L.; Glor, R.E.; Turelli, M. Environmental niche equivalency versus conservatism: Quantitative approaches to niche evolution. Evolution: Int. J. Org. Evol. 2008, 62, 2868–2883. [Google Scholar] [CrossRef]
  53. Muñoz-Mendoza, C.; D’Elía, G.; Panzera, A.; Villalobos-Leiva, A.; Sites, J.W., Jr.; Victoriano, P.F. Geography and past climate changes have shaped the evolution of a widespread lizard from the Chilean hotspot. Mol. Phylogenet. Evol. 2017, 116, 157–171. [Google Scholar] [CrossRef]
  54. Walther, G.R.; Post, E.; Convey, P.; Menzel, A.; Parmesan, C.; Beebee, T.J.; Fromentin, J.M.; Hoegh-Guldberg, O.; Bairlein, F. Ecological responses to recent climate change. Nature 2002, 416, 389–395. [Google Scholar] [CrossRef]
  55. Thuiller, W.; Broennimann, O.; Hughes, G.; Alkemade, J.R.M.; Midgley, G.F.; Corsi, F. Vulnerability of African mammals to anthropogenic climate change under conservative land transformation assumptions. Glob. Change Biol. 2006, 12, 424–440. [Google Scholar] [CrossRef]
  56. Levinsky, I.; Skov, F.; Svenning, J.C.; Rahbek, C. Potential impacts of climate change on the distributions and diversity patterns of European mammals. Biodiv. Conserv. 2007, 16, 3803–3816. [Google Scholar] [CrossRef]
  57. Ogawa-Onishi, Y.; Berry, P.M.; Tanaka, N. Assessing the potential impacts of climate change and their conservation implications in Japan: A case study of conifers. Biol. Conserv. 2010, 143, 1728–1736. [Google Scholar] [CrossRef]
  58. Khanum, R.; Mumtaz, A.S.; Kumar, S. Predicting impacts of climate change on medicinal asclepiads of Pakistan using Maxent modeling. Acta Oecologica 2013, 49, 23–31. [Google Scholar] [CrossRef]
  59. Abolmaali, S.M.R.; Tarkesh, M.; Bashari, H. MaxEnt modeling for predicting suitable habitats and identifying the effects of climate change on a threatened species, Daphne mucronata, in central Iran. Ecol. Inf. 2018, 43, 116–123. [Google Scholar] [CrossRef]
  60. Kadmon, R.; Farber, O.; Danin, A. Effect of roadside bias on the accuracy of predictive maps produced by bioclimatic models. Ecol. Appl. 2004, 14, 401–413. [Google Scholar] [CrossRef]
  61. Segurado, P.; Araujo, M.B.; Kunin, W.E. Consequences of spatial autocorrelation for nichebased models. J. Appl. Ecol. 2006, 43, 433–444. [Google Scholar] [CrossRef]
  62. Khan, A.M.; Li, Q.; Saqib, Z.; Khan, N.; Habib, T.; Khalid, N.; Majeed, M.; Tariq, A. MaxEnt Modelling and Impact of Climate Change on Habitat Suitability Variations of Economically Important Chilgoza Pine (Pinus gerardiana Wall.) in South Asia. Forests 2022, 13, 715. [Google Scholar] [CrossRef]
  63. Ali, F.; Khan, N.; Khan, A.M.; Ali, K.; Abbas, F. Species distribution modelling of Monotheca buxifolia (Falc.) A. DC.: Present distribution and impacts of potential climate change. Heliyon 2023, 9, e13417. [Google Scholar] [CrossRef]
  64. Kabir, M.; Hameed, S.; Ali, H.; Bosso, L.; Din, J.U.; Bischof, R.; Redpath, S.; Nawaz, M.A. Habitat suitability and movement corridors of grey wolf (Canis lupus) in Northern Pakistan. PLoS ONE 2017, 12, e0187027. [Google Scholar] [CrossRef]
  65. Haq, S.M.; Yaqoob, U.; Calixto, E.S.; Kumar, M.; Rahman, I.U.; Hashem, A.; Abd_Allah, E.F.; Alakeel, M.A.; Alqarawi, A.A.; Abdalla, M.; et al. Long-term impact of transhumance pastoralism and associated disturbances in high-altitude forests of Indian Western Himalaya. Sustainability 2021, 13, 12497. [Google Scholar] [CrossRef]
  66. Haq, S.M.; Calixto, E.S.; Yaqoob, U.; Ahmed, R.; Mahmoud, A.H.; Bussmann, R.W.; Mohammed, O.B.; Ahmad, K.; Abbasi, A.M. Traditional usage of wild fauna among the local inhabitants of Ladakh, Trans-Himalayan Region. Animals 2020, 10, 2317. [Google Scholar] [CrossRef] [PubMed]
  67. Hooper, D.U.; Adair, E.C.; Cardinale, B.J.; Byrnes, J.E.K.; Hungate, B.A.; Matulich, K.L.; Gonzalez, A.; Duffy, J.E.; Gamfeldt, L.; Connor, M.I. A global synthesis reveals biodiversity loss as a major driver of ecosystem change. Nature 2012, 486, 105–108. [Google Scholar] [CrossRef] [PubMed]
  68. Haq, S.M.; Yaqoob, U.; Majeed, M.; Amjad, M.S.; Hassan, M.; Ahmad, R.; Waheed, M.; Bussmann, R.W.; Soares Calixto, E.; Proćków, J.; et al. Quantitative ethnoveterinary study on plant resource utilization by indigenous communities in high-altitude regions. Front. Vet. Sci. 2022, 9, 944046. [Google Scholar] [CrossRef]
  69. Kanagaraj, R.; Araujo, M.B.; Barman, R.; Davidar, P.; De, R.; Digal, D.K.; Gopi, G.V.; Johnsingh, A.J.T.; Kakati, K.; Kramer-Schadt, S.; et al. Predicting range shifts of Asian elephants under global change. Div. Distrib. 2019, 25, 822–838. [Google Scholar] [CrossRef]
  70. Waheed, M.; Arshad, F.; Majeed, M.; Haq, S.M.; Aziz, R.; Bussmann, R.W.; Ali, K.; Subhan, F.; Jones, D.A.; Zaitouny, A. Potential distribution of a noxious weed (Solanum viarum Du-nal), current status, and future invasion risk based on MaxEnt modeling. Geol. Ecol. Landsc. 2023, 1–16. [Google Scholar] [CrossRef]
  71. Yamaura, Y.; Higa, M.; Senzaki, M.; Koizumi, I. Can charismatic megafauna be surrogate species for biodiversity conservation? Mechanisms and a test using citizen data and a hierarchical community model. In Biodiversity Conservation Using Umbrella Species: Blakiston’s Fish Owl and the Red-Crowned Crane; Nakamura, F., Ed.; Springer: Singapore, 2018; pp. 151–179. [Google Scholar]
  72. Haq, S.M.; Hassan, M.; Jan, H.A.; Al-Ghamdi, A.A.; Ahmad, K.; Abbasi, A.M. Traditions for Future Cross-National Food Security—Food and Foraging Practices among Different Native Communities in the Western Himalayas. Biology 2022, 11, 455. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Study area showing the Himalayan mountain range and recorded presence points of the Himalayan goral in South Asia.
Figure 1. Study area showing the Himalayan mountain range and recorded presence points of the Himalayan goral in South Asia.
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Figure 2. Pearson correlation heat map showing the pairwise correlation of climatic and biophysical variables (threshold; r = ±0.8) used in the distribution modeling of Himalayan goral.
Figure 2. Pearson correlation heat map showing the pairwise correlation of climatic and biophysical variables (threshold; r = ±0.8) used in the distribution modeling of Himalayan goral.
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Figure 3. Graph depicting AUC-ROC value of the current climate (1970s–2000s) MaxEnt model. The model’s precision was 0.965.
Figure 3. Graph depicting AUC-ROC value of the current climate (1970s–2000s) MaxEnt model. The model’s precision was 0.965.
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Figure 4. MaxEnt model for Himalayan goral using the jackknife of regularized training gain to determine the predictive strength of environmental variables.
Figure 4. MaxEnt model for Himalayan goral using the jackknife of regularized training gain to determine the predictive strength of environmental variables.
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Figure 5. Response curves of highly contributing variable in the MaxEnt distribution modeling of Himalayan goral. Bio 12 (annual precipitation); elevation; bio 14 (precipitation of driest month); aspect; bio 06 (minimum temperature of the coldest month); slope; bio 18 (precipitation of warmest quarter); bio 07 (temperature annual range).
Figure 5. Response curves of highly contributing variable in the MaxEnt distribution modeling of Himalayan goral. Bio 12 (annual precipitation); elevation; bio 14 (precipitation of driest month); aspect; bio 06 (minimum temperature of the coldest month); slope; bio 18 (precipitation of warmest quarter); bio 07 (temperature annual range).
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Figure 6. MaxEnt prediction map displaying the potential habitat suitability classification of Himalayan goral in the study area under current climatic (1970s–2000s) conditions.
Figure 6. MaxEnt prediction map displaying the potential habitat suitability classification of Himalayan goral in the study area under current climatic (1970s–2000s) conditions.
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Figure 7. MaxEnt prediction maps displaying the habitat suitability classes under future climate change scenario (A = SSPs-245 of 2050s; B = SSPs-585 of 2050s; C = SSPs-245 of 2070s; D = SSPs-585 of 2070s).
Figure 7. MaxEnt prediction maps displaying the habitat suitability classes under future climate change scenario (A = SSPs-245 of 2050s; B = SSPs-585 of 2050s; C = SSPs-245 of 2070s; D = SSPs-585 of 2070s).
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Table 1. Environmental factors selected after preliminary processing and their contribution rates.
Table 1. Environmental factors selected after preliminary processing and their contribution rates.
DescriptionCodePercent Contribution
Annual Precipitationbio1238.2
Elevationelev32.2
Precipitation of Driest Monthbio1411
Aspectspect8.2
Min. Temperature of Coldest Monthbio064.6
Slopeslope2.5
Precipitation of Warmest Quarterbio182.1
Temperature Annual Rangebio071.3
Table 2. The predicted probability of habitat suitability of the Himalayan goral under different climate change scenarios.
Table 2. The predicted probability of habitat suitability of the Himalayan goral under different climate change scenarios.
Climate Change ScenarioPredicted Probability of Occurrence of Himalayan Goral under Considered Habitat Suitability Classes
Not Suitable Least Moderate High Very HighTotal Suitable Land Area (km2)
(p ≤ 0.2)(p 0.21–0.4)(p 0.41–0.6)(p 0.61–0.8)(p ≥ 0.81)
Current climate515,79925,20024,11323,595629479,201
SSPs_245_2050512,85421,12924,78115,77520,46182,146
Rate of change (%)−0.6−17.62.7−40.3117.93.7
SSPs_585_2050505,98921,81019,07620,17127,95389,011
Rate of change (%)−1.9−14.4−23.4−15.7149.111.7
SSPs_245_2070508,79219,31917,18219,64230,06586,208
Rate of change (%)−1.4−26.6−33.9−18.3156.48.5
SSPs_585_2070504,85721,03419,82921,00628,27590,143
Rate of change (%)−2.14−18.07−19.56−11.62150.2412.94
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Haq, S.M.; Waheed, M.; Ahmad, R.; Bussmann, R.W.; Arshad, F.; Khan, A.M.; Casini, R.; Alataway, A.; Dewidar, A.Z.; Elansary, H.O. Climate Change and Human Activities, the Significant Dynamic Drivers of Himalayan Goral Distribution (Naemorhedus goral). Biology 2023, 12, 610. https://doi.org/10.3390/biology12040610

AMA Style

Haq SM, Waheed M, Ahmad R, Bussmann RW, Arshad F, Khan AM, Casini R, Alataway A, Dewidar AZ, Elansary HO. Climate Change and Human Activities, the Significant Dynamic Drivers of Himalayan Goral Distribution (Naemorhedus goral). Biology. 2023; 12(4):610. https://doi.org/10.3390/biology12040610

Chicago/Turabian Style

Haq, Shiekh Marifatul, Muhammad Waheed, Riyaz Ahmad, Rainer W. Bussmann, Fahim Arshad, Arshad Mahmood Khan, Ryan Casini, Abed Alataway, Ahmed Z. Dewidar, and Hosam O. Elansary. 2023. "Climate Change and Human Activities, the Significant Dynamic Drivers of Himalayan Goral Distribution (Naemorhedus goral)" Biology 12, no. 4: 610. https://doi.org/10.3390/biology12040610

APA Style

Haq, S. M., Waheed, M., Ahmad, R., Bussmann, R. W., Arshad, F., Khan, A. M., Casini, R., Alataway, A., Dewidar, A. Z., & Elansary, H. O. (2023). Climate Change and Human Activities, the Significant Dynamic Drivers of Himalayan Goral Distribution (Naemorhedus goral). Biology, 12(4), 610. https://doi.org/10.3390/biology12040610

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