Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-24T18:31:17.724Z Has data issue: false hasContentIssue false

Predicted distribution of the endemic fern Elaphoglossum beddomei reveals threats to rainforests of Western Ghats of India

Published online by Cambridge University Press:  12 November 2024

R. Thulasi
Affiliation:
Department of Quality Control, National Ayurveda Research Institute for Panchakarma (under CCRAS, Ministry of AYUSH, Government of India), Thrissur, Kerala, India PG & Research Department of Botany, The Zamorin’s Guruvayurappan College (affiliated to University of Calicut), Kozhikode, Kerala 673014, India
Francois Munoz
Affiliation:
Laboratoire Interdisciplinaire de Physique, Université Grenoble-Alpes, Grenoble, France
E.R. Sreekumar
Affiliation:
Department of Wildlife Science, College of Forestry, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala 680656, India
Maya C. Nair
Affiliation:
Post Graduate & Research Department of Botany, Government Victoria College (affiliated to University of Calicut), Palakkad, Kerala 678001, India Government Arts and Science College, Tholanur (affiliated to University of Calicut), Palakkad, Kerala 678722, India
K.P. Rajesh*
Affiliation:
PG & Research Department of Botany, The Zamorin’s Guruvayurappan College (affiliated to University of Calicut), Kozhikode, Kerala 673014, India
*
Corresponding author: K. P. Rajesh; Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Pteridophytes are excellent ecological indicators of habitat quality. In this study, we built a model that predicts the habitat suitability of Elaphoglossum beddomei Sledge, an epiphytic or lithophytic and endemic pteridophyte in Southern Western Ghats, by using the technique of species distribution modelling. The occurrence data of E. beddomei from field explorations as well as from various herbaria were collected during 2018–2022. These occurrence data along with climatic data were processed by R packages. The processed data were further analysed using MaxEnt software to project the distribution of E. beddomei in future climatic scenarios. After correlation analysis, five bioclimatic variables – Mean Temperature of Wettest Quarter (bio8), Precipitation of Driest Quarter (bio17), Precipitation of Warmest Quarter (bio18), Precipitation of Wettest Quarter (bio16) and Temperature Annual Range (BIO5-BIO6) (bio7) – were selected from 19 bioclimatic variables with less correlation. Precipitation of Warmest Quarter (bio18) had the most influence in determining the distribution of E. beddomei, with a permutation importance of 83%. Conversely, Temperature Annual Range (BIO5-BIO6) (bio7) and Precipitation of Driest Quarter (bio17) showed least influence in determining the distribution of E. beddomei, and hence, the models created without these variables are considered for prediction. The habitat suitability predictions of the model indicate that the potential habitats of the species may get reduced in Southern Western Ghats in future climatic scenarios. It is in tune with the predicted expansion of drier climatic zones in Southern Western Ghats, which may reduce the suitable habitats for the E. beddomei in near future. So, it demands formulating suitable strategies for reducing the emission of greenhouse gases, regenerating forests and conserving forests by implementing more stringent policies on the environment to protect such highly habitat-specific evergreen elements.

Type
Research Article
Copyright
© The Author(s), 2024. Published by Cambridge University Press

Introduction

Pteridophytes play significant roles in ecosystems by providing suitable microhabitats for other plants and animals, preventing nutrient leaching and soil erosion, in succession and as gap fillers in most habitats (Holttum Reference Holttum1938; Walker Reference Walker1994; Sharpe et al. Reference Sharpe, Mehltreter, Walker, Mehltreter, Walker and Sharpe2010; Walker and Sharpe Reference Walker, Sharpe, Mehltretter, Walker and Sharpe2010; Walker et al. Reference Walker, Mehltretter, Sharpe, Mehltretter, Walker and Sharpe2010). They prefer specific environments with definite habitat traits to thrive and establish. Due to these differential preferences for specific ecological conditions, many of them are endemic to certain bio-geographic regions and habitats (Sharpe et al. Reference Sharpe, Mehltreter, Walker, Mehltreter, Walker and Sharpe2010; Pouteau et al. Reference Pouteau, Meyer and Blanchard2016; Karger et al. Reference Karger, Kessler and Lehnert2021b).

There are two major centres of diversity of pteridophytes in India – Western Ghats and North East India – and approximately 10% of Indian pteridophytes are endemics. Majority of the taxa are confined to the Western Ghats of the Peninsular India, due to high degree of habitat diversity, as a result of its unique geographical location and climatic features (Fraser-Jenkins, Reference Fraser-Jenkins2008).

Expansion of drier areas at a higher rate and associated changes are expected in the immediate future (Antão et al. Reference Antao, Bates, Blowes, Waldock, Supp, Magurran, Dornelas and Schipper2020) and the Western Ghats of Peninsular India is also not an exception (Munoz et al. Reference Munoz, Estopinan and Bose2021). The alterations in climatic conditions specifically affect the existence of endemics. Large-scale climatic changes due to an increase in average temperature and its influence on the vegetation of the Earth were predicted by various climate change models (Masson-Delmotte Reference Masson-Delmotte2018).

As endemics have restricted distribution in small geographical areas, they usually face serious threats to their existence. By analysing the known geographical locations of a taxon, many studies made use of Maximum Entropy (MaxEnt) modelling to get insights into patterns of species distribution, including potential areas (Bose et al. Reference Bose, Munoz and Ramesh2016; Chaitanya and Meiri Reference Chaitanya and Meiri2021; Ferreira et al. Reference Ferreira, Almeida and Quintela-Sabarís2021; Karger et al. Reference Karger, Conrad and Böhner2021a). This warrants development of specific conservation strategies for such species and this is possible only through the basic know-how on its pattern of distribution in different habitats.

The MaxEnt modelling has been widely used in India and elsewhere to predict the changes in distribution of species in response to climate changes (Phillips et al. Reference Phillips, Anderson and Schapire2006; Phillips et al. Reference Phillips, Anderson and Dudík2017; Munoz et al. Reference Munoz, Estopinan and Bose2021). It ranged from analysing the future prospects of crops such as rubber (Ray et al. Reference Ray, Behera and Jacob2014), pepper (Sen et al. Reference Sen, Gode and Ramanujam2016), Kaempferia (Raina et al. Reference Raina, Abraham and Sivaraj2015), tea (Potom and Nimasow Reference Potom and Nimasow2019), Zingiber (Huang et al. Reference Huang, Xie and Wang2019), medicinal plants – Asclepiads in Africa (Khanum et al. Reference Khanum, Mumtaz and Kumar2013), Coscinium fenestratum and Embelia ribes (Pownitha et al. Reference Pownitha, Nagaraja, Charles, Vasudeva, Aravind and Ravikanth2022), Garcinia indica (Palkar et al. Reference Palkar, Janarthanam and Sellappan2020) in Western Ghats, Taxus contorta in Himalayan region (Chauhan et al. Reference Chauhan, Ghoshal, Kanwal, Sharma and Ravikanth2022), Bauhinia vahlii in Indian subcontinent (Thakur et al. Reference Thakur, Bhat, Kumar, Ravikanth and Saikia2022), Terminalia chebula (Kailash et al. Reference Kailash, Charles, Ravikanth, Setty and Kadirvelu2022), to predict the expansion of invasive plants like Mimosa diplotricha, Mikania micrantha (Choudhury et al. Reference Choudhury, Deb and Singha2016), Parthenium (Arogoundade et al. Reference Arogoundade, Odindi and Mutanga2020), etc., and animals such as African snail (Sarma et al. Reference Sarma, Munsi and Ananthram2015), pests (Choudhary et al. Reference Choudhary, Mali and Fand2019), diseases (Escobar et al. Reference Escobar, Lira-Noriega and Medina-Vogel2014), and for conservation planning of threatened (Sreekumar et al. Reference Sreekumar, Suganthasakthivel and Sreejith2016) and endemic taxa – Calamus spp. (Joshi et al. Reference Joshi, Charles and Ravikanth2017), Rosa arabica (Abdelaal et al. Reference Abdelaal, Fois, Fenu and Bacchetta2019), etc. Species distribution modelling (SDM) studies of pteridophytes, however, are comparatively less frequent (Sharpe Reference Sharpe2019; Della and Falkenberg Reference Della and Falkenberg2019). SDMs of pteridophytes have been attempted in the island of Taiwan (Hsu et al. Reference Hsu, Tamis and Raes2012; Hsu et al. Reference Hsu, Oostermeijer and Wolf2014; Hsu et al. Reference Hsu, Wolf and Tamis2014), Neotropical region (Brummitt et al. Reference Brummitt, Aletrari and Syfert2016) and Mesoamerican region (Syfert et al. Reference Syfert, Brummitt and Coomes2018). Shreshta and Zhang (Reference Shrestha and Zhang2015) used SDM to predict the extent of distribution of Huperzia hamiltonii, a Himalayan endemic.

In the present study, the distribution of endemic fern species Elaphoglossum beddomei is predicted by using the bioclimatic variables for two time periods – current climatic regime and one future climatic regime (2041–2070). It was categorised as least concern (LC) in an earlier assessment (Kumar Reference Kumar2011). Later assessments (Chandra et al. Reference Chandra, Fraser-Jenkins and Kumari2008; Ebihara et al. Reference Ebihara, Fraser-Jenkins and Parris2012; Fraser-Jenkins et al. Reference Fraser-Jenkins, Gandhi and Kholia2021) treated the taxon as near threatened (NT). According to Karger et al. (Reference Karger, Kessler and Lehnert2021b), loss of tropical cloud forest biodiversity is at its fastest rate now, due to worldwide climate change and limited protection actions. Such loss of biodiversity in montane evergreen forests may adversely affect the existence of endemics inhabited in such specific ecosystems, like E. beddomei.

E. beddomei is a high-altitude, evergreen-shola element in the Western Ghats of Peninsular India. So, the present study is focused on finding out the potential habitat for E. beddomei in the current climatic scenario. This study also aims to find out the important bioclimatic variables that determine the habitat suitability of E. beddomei in Southern Western Ghats and an attempt is being made to figure out the habitat suitability change that should occur in the light of climate change.

Materials and methods

Distribution data of E. beddomei Sledge was tabulated from the available literature (Fraser-Jenkins et al. Reference Fraser-Jenkins, Gandhi and Kholia2021; Hassler Reference Hassler2024; Manickam and Irudayaraj Reference Manickam and Irudayaraj1992; Nayar and Geevarghese Reference Nayar and Geevarghese1993), herbaria (CALI, KFRI, MH, ZGC) and field observations (Table S 1). It is an endemic fern with simple fronds, crowded on the short creeping (0.5 cm thick) rhizome and growing in the evergreen and shola forests of the Western Ghats of Peninsular India as epiphytes or lithophytes at an elevation of 900–2200 m (see supplementary data for description of the species S1). It is sparsely distributed in the Western Ghats of the Peninsular Indian states of Kerala, Tamil Nadu and Karnataka. GPS data points were obtained from the field observations during 2018–2021 (Figure 1). Position coordinates, latitude and longitude, were recorded using a mobile phone geopositioning application. Co-located or nearby locations (Phillips et al. Reference Phillips, Anderson and Dudík2017), within 2 km, were avoided for better results, totalling 31 records of E. beddomei, including primary collection records (Figure 1).

Figure 1. The background map generated based on the evergreen forest patches in Southern Western Ghats (Indian Biodiversity Information System https://www.indiaobservatory.org.in/tool/ibis) showing the distribution locations of Elaphoglossum beddomei in Southern Western Ghats (yellow dots); predicted potential habitat of E. beddomei in current climatic regime (dark blue regions); the background with existing evergreen forest patches (light blue regions).

Environmental data

High-resolution climatic data of 19 bioclimatic variables for two time periods – 2011–2040 (current) and 2041–2070 – from the CHELSA (Climatologies at high resolution for the Earth’s land surface areas) CMIP6 by Karger et al. (2017) were selected, as environmental predictors. Two scenarios of future climate were selected as SSP126 and SSP585 representing seasonality, annual trends in climate and limiting environmental factors (Qi et al. Reference Qi, Wei and Yansui2004). The Shared Socio-economic Pathways (SSP) derive the emission scenarios under different climate policies. SSP126 stands for SSP1-RCP2.6 climate as simulated by the GCMs. Here, RCP is the Representative Concentration Pathway, which is a greenhouse gas emission trajectory by the IPCC. SSP126, RCP2.6 is the lowest in the RCPs; it assumes a decreased emission of greenhouse gases after 2100. Conversely, SSP585, SSP5-RCP8.5 climate as simulated by GCMs, represents a more pessimistic scenario of future gas emission. RCP8.5 represents the concentration of carbon, which delivers global warming at an average of 8.5 Watts/sq. metre across the earth (Karger et al. Reference Karger, Conrad and Böhner2021a). We eliminated the highly correlated – both positively and negatively correlated variables – with a Pearson correlation coefficient > 0.75, for avoiding overprediction and confounding effects in the model (Elith et al. Reference Elith, Phillips and Hastie2011; Merow et al. Reference Merow, Smith and Silander2013; Bose et al. Reference Bose, Munoz and Ramesh2016).

Background selection

The first and most crucial step in SDM is the choice of background points, or landscape selection, which should represent a broad array of possible habitats for the species (Sreekumar and Nameer, Reference Sreekumar and Nameer2021, Reference Sreekumar and Nameer2022). So in this study, the background has been selected within the evergreen and shola forest vegetation of Southern Western Ghats – representing a potential habitat for E. beddomei – from the vegetation map of Indian Institute of Remote Sensing Biodiversity Information System, Government of India (Roy et al. Reference Roy, Meiyappan and Joshi2016).

MaxEnt modelling

We used MaxEnt version 3.4.1 (Phillips and Dudik, Reference Phillips and Dudik2008) to perform a species distribution model of E. beddomei. The best model was evaluated based on True Skill Statistics (TSS) and overall accuracy, calculated using R package ENMTools (Chaitanya and Meiri, Reference Chaitanya and Meiri2021), and Area Under the receiver operating characteristic Curve (AUC) from MaxEnt output. The model that showed highest values for AUC, TSS and overall accuracy was selected as the best MaxEnt model for analysis (Table S 2).

The initial model was created using MaxEnt based on the regularisation multiplier value (rm value = 3) as calculated by the ecological niche modelling (ENM) evaluation tool. Then, based on jackknife analysis in the MaxEnt output, we calculated the contribution permutation importance of each variable and discarded the lowest valued variable (Zurell et al. Reference Zurell, Franklin and König2020) and again ran MaxEnt to get the best model with highest AUC, TSS and overall accuracy. The MaxEnt settings were given as 10-fold of cross-validation, number of background points of 10,000 and iterations of 5,000. The output file format was set as complementary log-log (c-loglog).

Future distribution prediction of E. beddomei

The current study predicted the distribution of E. beddomei in future climatic regimes (2041–2070) under different climatic change scenarios – such as SSP126 and SSP585 for 2041–2070. Here, we used five Earth System Models (ESMs) under CMIP6 (Coupled Model Intercomparison Project Phase-6) – including GFDL-ESM4, UKESM 1-OLL, MPI-ESM 1-2HR, IPSLL-CM6A LR and MRI-ESM 2-0. Then we calculated the average of these ESMs.

Evaluation of the MaxEnt model

We evaluated the MaxEnt models based on the AUC, which plots sensitivity against 1-specificity. It ranges from 0 to 1; the value near one indicates the best prediction. We also considered TSS, which is ‘sensitivity + specificity – 1’, and the overall accuracy for model performance, using R package ENMTools.

Habitat loss and gain in future simulations

We mapped suitable and unsuitable habitats of E. beddomei by considering the threshold value of maximum test sensitivity plus specificity c-loglog threshold (Max SSS) (Liu et al. Reference Liu, White and Newell2013) on the predicted probabilities, using the Raster reclassification tool in Q-GIS v. 3.61. Then, we used the raster calculator tool of Q-GIS v. 3.61 to calculate changes in suitable habitats of E. beddomei, as the difference between the current binary map and future binary maps under different conditions in future climatic regimes. Based on the prediction of potential habitats, we calculated the habitat loss and gain in the future time periods, by comparing the predicted suitable area under two climatic scenarios – SSP126 and SSP585 – of 2041–2070 and the prediction in the current time period. From this calculation, we obtained the gain of suitable habitat, loss of suitable habitat and unchanged habitats of E. beddomei in future climatic conditions.

Results

MaxEnt modelling and influenced bioclimatic variables

After correlation analysis, five bioclimatic variables – Mean Temperature of Wettest Quarter (bio8), Precipitation of Driest Quarter (bio17), Precipitation of Warmest Quarter (bio18), Precipitation of Wettest Quarter (bio16) and Temperature Annual Range (BIO5-BIO6) (bio7) – were selected from 19 bioclimatic variables with less correlation. As per the jackknife analysis, Precipitation of Warmest Quarter (bio18) had the most influence in determining the distribution of E. beddomei, with a permutation importance of 83% (Table 1). Temperature Annual Range (BIO5-BIO6) (bio7) and Precipitation of Driest Quarter (bio17) showed least influence in determining the distribution of E. beddomei, and hence, the models created without these variables were considered for prediction.

Table 1. Contribution of selected bioclimatic variables to the distribution of E. beddomei in current climatic regime

MaxEnt modelling

The predicted model had an AUC value of 0.838, TSS value of 0.6852 and overall accuracy of 0.9346. Predicted distribution in current climatic regimes represented its potential distribution along the Western Ghats (Figure 1). The results showed that the predicted suitable area for E. beddomei at present is approximately about 11,181.6 square km in Southern Western Ghats.

Predicted changes in future climatic scenarios

Here, Table 2 summarises the potential habitat gain and loss or Niche shift in the future climatic period – 2041–2070 – compared with the current climatic regime. Here in all climatic scenarios, habitat loss was more than that of habitat gain in future time periods, such as in the 2041–2070 climatic period, the average loss of suitable habitat in two scenarios was 19.769% and the average gain of suitable habitats in two scenarios was only 0.5205%. The loss of suitable habitat was greater in SSP126 (20.718%) climatic scenario of 2041–2070 time period. Niche shift of E. beddomei is very negligible in future climatic periods, as average habitat gain is 0.5205%. (Table 2).

Table 2. Habitat loss and gain in 2041–2070 time period

Discussion

At present, E. beddomei is known to occur in a narrow zone of the Western Ghats of Kerala, Tamil Nadu and Karnataka with specific cool, evergreen, climatic parameters (Manickam and Irudayaraj, Reference Manickam and Irudayaraj1992; Benniamin and Sundari, Reference Benniamin and Sundari2020; Benniamin et al. Reference Benniamin, Bhagathsingh, Sundari and Jesubalan2020). E. beddomei is known to be endemic to Southern Western Ghats of India. As per earlier IUCN Red List assessment (Kumar, Reference Kumar2011), it was considered as LC and demanded further studies to clarify its geographic distribution, and in recent assessments, the status was redesignated as NT (Benniamin et al. Reference Benniamin, Bhagathsingh, Sundari and Jesubalan2020; Fraser-Jenkins et al. Reference Fraser-Jenkins, Gandhi and Kholia2021). The global trend in forest ecosystems showed that the concentration of the evergreen forests is confined more to higher altitudes and shows drastic decline at higher rates (Laurance et al. Reference Laurance, Useche and Rendeiro2012), causing severe loss of tropical cloud forest ecosystems (Murugan et al. Reference Murugan, Shetty and Anandhi2009; Karger et al. Reference Karger, Kessler and Lehnert2021b), which may adversely affect most of the high-altitude evergreen endemic species (Munoz et al. Reference Munoz, Estopinan and Bose2021). So, E. beddomei, a species inhabiting evergreen habitat, may become more threatened in future climatic regimes due to lack of suitable habitats.

The predicted potential habitats in current climatic regimes showed a possibility of recording E. beddomei from other potential habitats of the Western Ghats. There are similar reports of rediscoveries and extended distribution records found by the analysis of occurrence of species like Micromeria serbaliana and Veronica kaiseri (Omar and Elgamal Reference Omar and Elgamal2021) in Egypt, and ferns under Rare, Endangered and Threatened (RET) categories (Williams et al., Reference Williams, Seo and Thorne2009) in the United States through distribution models. Predicted potential distribution in the future climatic regime – 2041–2070 – showed a trend of decline for E. beddomei in Southern Western Ghats (Figure 2a and b), as the average loss of potential habitats in the 2041–2070 is 19.796%. Whereas, the average gain of potential habitats or niche shifts in the climatic period – 2041–2070 – is only 0.5205%.

Figure 2. Habitat gain-unchanged-loss map of E. beddomei in 2040–2071; a. SSP126 scenario and b. SSP585 scenario – black (1) indicated habitat gain; blue (0) indicated unchanged habitat; and red (–1) indicated habitat loss.

By analysing the influence of bioclimatic variables, the distribution of E. beddomei proved limited by precipitation (Table 1). As E. beddomei is an evergreen high-altitude fern species, the temperature and precipitation characteristics of high-altitude evergreen forests determine the growth and distribution. So, the predicted future distribution reflects a change in precipitation pattern in Southern Western Ghats, which in turn should affect the existence of E. beddomei in Southern Western Ghats. It can be concluded that the suitable habitat for E. beddomei will progressively decline in future due to the variations in global temperature and precipitation.

Although the forcing level differs between the 126 and 585 SSP scenarios, it does not mean that the predicted rainfall patterns should differ much between the two scenarios. For instance, under the CNRM-CM6-1 model, we found that the variation of bio12 (annual rainfall) and bio18 (rainfall of the warmest quarter) in 2060 between the two SSP scenarios should only be about 0.8% and 5.3% on average, respectively. This is why our predictions of occurrences of Elaphoglossum are quite similar between SSP scenarios (Munoz et al. Reference Munoz, Estopinan and Bose2021).

The study of endemics in Western Ghats by Bose et al. (2015) mentioned that the variation in precipitation patterns from past climatic regimes to current climatic conditions might be the reason for higher endemicity in Western Ghats, especially in Southern Western Ghats. So, the predicted future decline of E. beddomei from Southern Western Ghats points to a drastic change in precipitation pattern in Southern Western Ghats regions. Fluctuating rainfall patterns are due to increased global warming (Murugan et al. Reference Murugan, Shetty and Anandhi2009) and it may affect the existence of evergreen species like E. beddomei of Western Ghats. Increase in temperature and fluctuating or decreasing precipitation may act as limiting factors for such strict evergreen taxa. The changes in the distribution pattern of animals, birds or plants have been used to predict the trend in future environmental conditions in India and other countries (Jose and Nameer Reference Jose and Nameer2020; Sony et al. Reference Sony, Sen and Kumar2018; Li et al. Reference Li, Cao and He2019). The expansion of the Peafowl (Pavo cristatus) population in the Peninsular Indian state of Kerala (Jose and Nameer Reference Jose and Nameer2020) has been taken as an indication of desertification and increase in temperature regimes in the state of Kerala. Similarly, a reduction in suitable habitat due to climate change is anticipated for the endemic ungulate mammal, Nilgiri Tahr (Nilgiritragus hylocrius) population in the Western Ghats (Sony et al. Reference Sony, Sen and Kumar2018). The studies on plants, especially the impact of climate change on endemics and threatened category taxa, warn for establishing proper conservation strategies, in situ as well as ex situ, for the maintenance of threshold minimum population sizes globally. The potential distribution and impact of climate change on the endangered pteridophyte genus Isoetes (Yang et al. Reference Yang, Huang and Jiang2022) in China, the rare and endangered fern species Brainea insignis (Wanga et al. Reference Wanga, Lob and Changc2012) in Taiwan and the micro-endemic plant species Cistus ladanifer subsp. sulcatus (Ferreira et al. Reference Ferreira, Almeida and Quintela-Sabarís2021) in Portugal showed the reduction of potential habitats in future climatic regimes due to drastic changes in climatic conditions. Along with these predictions addressing the impact of climate change on species existence and distribution, there are studies that predict suitable habitats for endangered lycophytes and fern species for designing suitable conservation strategies (Wang et al. Reference Wang, Wan and Zhang2016; Li et al. Reference Li, Cao and He2019). These strategies will include in situ conservation by locating potential habitats and re-establishment of the species, as well as ex situ methods like procurement of such species from natural habitats and maintaining them in botanical gardens, along with germplasm conservation through cryobanks and spore banks. Likewise, E. beddomei is a NT, endemic species to the Western Ghats (Ebihara et al. Reference Ebihara, Fraser-Jenkins and Parris2012; Chandra et al. Reference Chandra, Fraser-Jenkins and Kumari2008; Benniamin et al. Reference Benniamin, Bhagathsingh, Sundari and Jesubalan2020; Fraser-Jenkins et al. Reference Fraser-Jenkins, Gandhi and Kholia2021). The decrease in potential habitats of E. beddomei in future climatic regime is an indication of the decline in evergreen forest patches in Southern Western Ghats. So, if the climate changes to an unfavourable condition, it may adversely affect the survival of the NT species – E. beddomei.

The present study provides deep insights on the trend of distribution of Pteridophytes and warrants for formulating suitable conservation strategies for taxa such as E. beddomei. Except for some preliminary attempts of in vitro spore germination and gametophyte development studies (Benniamin et al. Reference Benniamin, Bhagathsingh, Sundari and Jesubalan2020), the protocols for mass propagation and field trials for re-introduction of this species are yet to be formulated. Suitable strategies, both short-term and long-term, such as in situ strategies targeting conservation of the endemic species in their natural habitat using the support of local people and forest personnel, raise awareness to the public about the importance of the local biodiversity and its role in their life and future generations. Ex situ conservation methods like growing the plant in gardens by providing appropriate habitat conditions are essential to ensure the conservation of this species. The case of E. beddomei is also an indication of the trend of endemics of the Southern Western Ghats in the age of climate change (see also Munoz et al. Reference Munoz, Estopinan and Bose2021).

Conclusion

The predicted species distribution and ENM of the species – E. beddomei – carried out in the present study reveal trends in climatic variations in the near future in India, especially in the Western Ghats. The distribution model predicted that there will be subsequent increase in temperature and dryness in Southern Western Ghats due to climate change, and change in precipitation pattern will lead to drastic decline of suitable habitats for evergreen taxa such as E. beddomei. It is similar to the trends predicted for Peafowl (Jose and Nameer, Reference Jose and Nameer2020) and Nilgiri Tahr (Sony et al. Reference Sony, Sen and Kumar2018) in southern India. Hence, suitable conservation strategies are essential to reduce the rate of degradation of critical habitats such as evergreen forests in Peninsular India along with protecting the micro habitats of taxa that serve as ecological indicators.

Supplementary material

The supplementary material for this article can be found at https://doi.org/10.1017/S0266467424000154

Acknowledgements

We are thankful to the authorities of the Zamorin’s Guruvayurappan College, Kozhikode, Kerala, and Government Victoria College, Palakkad, Kerala, along with the Director of Collegiate Education, Govt. of Kerala, for facilities and support. Thanks are due to the Kerala Forest and Wildlife Department for the permission and support during the field studies. The first author (TR) acknowledges the Council for Scientific and Industrial Research (CSIR), Human Resource Development Group, New Delhi, for the financial support, and the authorities of Central Council for Research in Ayurvedic Sciences (CCRAS), New Delhi, and National Ayurveda Research Institute for Panchakarma, Cheruthuruthy, Thrissur, Kerala, under CCRAS, Ministry of AYUSH, Government of India for support.

Competing interests

The author(s) declare none.

References

Abdelaal, M, Fois, M, Fenu, G and Bacchetta, G (2019) Using MaxEnt modeling to predict the potential distribution of the endemic plant Rosa arabica Crép. Egypt. Ecological Informatics 50, 6875.CrossRefGoogle Scholar
Antao, LH, Bates, AE, Blowes, SA, Waldock, C, Supp, SR, Magurran, AE, Dornelas, M and Schipper, AM (2020) Temperature-related biodiversity changes across temperate marine and terrestrial systems. Nature Ecology & Evolution 4, 927933.CrossRefGoogle ScholarPubMed
Arogoundade, AM, Odindi, J and Mutanga, O (2020) Modelling Parthenium hysterophorus invasion in KwaZulu-Natal province using remotely sensed data and environmental variables. Geocarto International 35, 14501465.CrossRefGoogle Scholar
Benniamin, A, Bhagathsingh, C, Sundari, MS and Jesubalan, D (2020) Spore germination and early gametophyte development of an endemic fern, Elaphoglossum beddomei Sledge. Indian Fern J 37, 246251.Google Scholar
Benniamin, A and Sundari, MS (2020) Pteridophytes of Western Ghats- A Pictorial Guide. Dehra Dun: Bishen Singh Mahendra Pal Singh.Google Scholar
Indian Biodiversity Information System https://www.indiaobservatory.org.in/tool/ibis.Google Scholar
Bose, R, Munoz, F, Ramesh, BR, et al. (2016) Past potential habitats shed light on the biogeography of endemic tree species of the Western Ghats biodiversity hotspot, South India. Journal of Biogeography 43, 899910.CrossRefGoogle Scholar
Brummitt, N, Aletrari, E, Syfert, MM, et al. (2016) Where are threatened ferns found? Global conservation priorities for pteridophytes. Journal of Systematics Evolution 54, 604616.CrossRefGoogle Scholar
Chaitanya, R and Meiri, S (2021) Can’t see the wood for the trees? Canopy physiognomy influences the distribution of peninsular Indian Flying lizards. Journal of Biogeography 49, 113.CrossRefGoogle Scholar
Chandra, S, Fraser-Jenkins, CR, Kumari, A, et al. (2008) A summary of the status of threatened pteridophytes of India. Taiwania 53, 170209.Google Scholar
Chauhan, S, Ghoshal, S, Kanwal, KS, Sharma, V and Ravikanth, G (2022) Ecological niche modelling for predicting the habitat suitability of endangered tree species Taxus contorta Griff. in Himachal Pradesh (Western Himalayas, India). Tropical Ecology 63(2), 300313.CrossRefGoogle Scholar
Choudhary, JS, Mali, SS, Fand, BB, et al. (2019) Predicting the invasion potential of indigenous restricted mango fruit borer, Citripestis eutraphera (Lepidoptera: Pyralidae) in India based on MaxEnt modelling. Current Science 25, 636.CrossRefGoogle Scholar
Choudhury, MR, Deb, P, Singha, H, et al. (2016) Predicting the probable distribution and threat of invasive Mimosa diplotricha Suavalle and Mikania micrantha Kunth in a protected tropical grassland. Ecological Engineering 1, 2331.CrossRefGoogle Scholar
Della, AP and Falkenberg, DD (2019) Pteridophytes as ecological indicators: an overview. Hoehnea 46, e522018.CrossRefGoogle Scholar
Ebihara, A, Fraser-Jenkins, CR, Parris, BS, et al. (2012) Rare and threatened pteridophytes of Asia 1. An enumeration of narrowly distributed taxa. Bull Natl Mus Nat Sci, Ser B 38, 93119.Google Scholar
Elith, J, Phillips, SJ, Hastie, T, et al. (2011) A statistical explanation of MaxEnt for ecologists. Diversity and Distributions 17, 4357.CrossRefGoogle Scholar
Escobar, LE, Lira-Noriega, A, Medina-Vogel, G, et al. (2014) Potential for spread of the white-nose fungus (Pseudogymnoascus destructans) in the Americas: use of MaxEnt and NicheA to assure strict model transference. Geospat 9, 221229.CrossRefGoogle ScholarPubMed
Ferreira, MR, Almeida, AM, Quintela-Sabarís, C, et al. (2021) The role of littoral cliffs in the niche delimitation on a microendemic plant facing climate change. PLoS One 16, 0258976.CrossRefGoogle ScholarPubMed
Fraser-Jenkins, CR (2008) Endemics and pseudo-endemics in Relation to the distribution patterns of Indian Pteridophytes. Taiwania 53, 264292.Google Scholar
Fraser-Jenkins, CR, Gandhi, KN, Kholia, BS, et al. (2021) An Annotated Checklist of Indian Pteridophytes Part 1. DehraDun: Bishen Singh Mahendra Pal Singh.Google Scholar
Hassler, M (2024) World Ferns. Synonymic Checklist and Distribution of Ferns and Lycophytes of the World. Version 18.4. Available at https://www.worldplants.de/ferns/ (accessed 9 October, 2024).Google Scholar
Holttum, R (1938) The ecology of tropical pteridophytes. In Verdoorn F (ed), Manualof Pteridology. DenHaag: Nijhoff.Google Scholar
Hsu, RC, Oostermeijer, JG and Wolf, JH (2014) Adaptation of a widespread epiphytic fern to simulated climate change conditions. Plant Ecol 1, 889897.CrossRefGoogle Scholar
Hsu, RC, Tamis, WL, Raes, N, et al. (2012) Simulating climate change impacts on forests and associated vascular epiphytes in a subtropical island of East Asia. Diversity and Distributions 18, 334347.CrossRefGoogle Scholar
Hsu, RC, Wolf, JH and Tamis, WL (2014) Regional and elevational patterns in vascular epiphyte richness on an East Asian island. Biotropica 46, 549555.CrossRefGoogle Scholar
Huang, Z, Xie, L, Wang, H, et al. (2019) Geographic distribution and impacts of climate change on the suitable habitats of Zingiber species in China. Industrial Crops and Products 5, 111429.CrossRefGoogle Scholar
Jose, SV and Nameer, PO (2020) The expanding distribution of the Indian Peafowl (Pavo cristatus) as an indicator of changing climate in Kerala, southern India: a modelling study using MaxEnt. Ecological Indicators 110, 105930.CrossRefGoogle Scholar
Joshi, M, Charles, B, Ravikanth, G, et al. (2017) Assigning conservation value and identifying hotspots of endemic rattan diversity in the Western Ghats, India. Plant Diversity 39, 263272.CrossRefGoogle ScholarPubMed
Kailash, BR, Charles, B, Ravikanth, G, Setty, S and Kadirvelu, K (2022) Identifying the potential global distribution and conservation areas for Terminalia chebula, an important medicinal tree species under changing climate scenario. Tropical Ecology 63(4), 584595.CrossRefGoogle Scholar
Karger, DN, Conrad, O, Böhner, J, et al. (2021a) Climatologies at high resolution for the earth’s land surface areas. Scientific Data 4, 170122.CrossRefGoogle Scholar
Karger, DN, Kessler, M, Lehnert, M, et al. (2021b) Limited protection and ongoing loss of tropical cloud forest biodiversity and ecosystems worldwide. Nature Ecology & Evolution 5, 854862.CrossRefGoogle ScholarPubMed
Khanum, R, Mumtaz, AS and Kumar, S (2013) Predicting impacts of climate change on medicinal asclepiads of Pakistan using MaxEnt modeling. Acta Oecol 49, 2331.CrossRefGoogle Scholar
Kumar, B (2011) Elaphoglossum Beddomei. Cambridge: The IUCN Red List of Threatened Species.Google Scholar
Laurance, WF, Useche, DC, Rendeiro, J, et al. (2012) Averting biodiversity collapse in tropical forest protected areas. Nature 489, 290294.CrossRefGoogle ScholarPubMed
Li, Y, Cao, W, He, X, et al. (2019) Prediction of suitable habitat for Lycophytes and Ferns in northeast China: a case study on Athyrium brevifrons . Chin Geogr Sci 29, 10111023.CrossRefGoogle Scholar
Liu, C, White, M and Newell, G (2013) Selecting thresholds for the prediction of species occurrence with presence-only data. Journal of Biogeography 40, 778789.CrossRefGoogle Scholar
Manickam, VS and Irudayaraj, V (1992) Pteridophyte Flora of the Western Ghats – South India. New Delhi: B. I. Publications Pvt. Ltd.Google Scholar
Masson-Delmotte, V (ed) (2018) Global Warming of 1.5oC: An IPCC Special Report on the Impacts of Global Warming of 1.5 C Above Pre-Industrial Levels and Related Global greenhouse Gas Emission Pathways, in the Context of Strengthening the Global Response to the Threat of Climate Change, Sustainable Development, and Efforts to Eradicate Poverty. Geneva: World Meteorological Organization.Google Scholar
Merow, C, Smith, MJ and Silander, J A (2013) A practical guide to MaxEnt for modeling species’ distributions: what it does, and why inputs and settings matter. Ecography 36, 10581069.CrossRefGoogle Scholar
Munoz, F, Estopinan, J, Bose, R, et al. (2021) Future impacts of climate change and deforestation on endemic trees of Western Ghats, South India. In On the Edge of Sixth Extinction in Biodiversity Hotspots: Facts, Needs, Solutions and Opportunities in Thailand and Adjacent Countries. Kolkata: CU Press.Google Scholar
Murugan, M, Shetty, PK, Anandhi, A, et al. (2009) Rainfall changes over tropical montane cloud forests of southern Western Ghats, India. Current Science 97, 17551760.Google Scholar
Nayar, BK and Geevarghese, KK (1993) Fern Flora of Malabar. New Delhi: Indus Publishing Company.Google Scholar
Omar, K and Elgamal, I (2021) IUCN red list and species distribution models as tools for the conservation of poorly known species: a case study of endemic plants Micromeria serbaliana and Veronica kaiseri in South Sinai, Egypt. Kew Bulletin 76, 477496.CrossRefGoogle Scholar
Palkar, RS, Janarthanam, MK and Sellappan, K (2020) Prediction of potential distribution and climatic factors influencing Garcinia indica in the Western Ghats of India using ecological niche modeling. National Academy Science Letters 43(6), 585591.CrossRefGoogle Scholar
Phillips, SJ, Anderson, RP, Dudík, M, et al. (2017) Opening the black box: an open-source release of MaxEnt. Ecography 40, 887893.CrossRefGoogle Scholar
Phillips, SJ, Anderson, RP and Schapire, RE (2006) Maximum entropy modeling of species geographic distributions. Ecological Modelling 190(3-4), 231259.CrossRefGoogle Scholar
Phillips, SJ and Dudik, M (2008) Modelling of species distributions with MaxEnt: new extensions and a comprehensive evaluation. Ecography 31, 161175.CrossRefGoogle Scholar
Potom, R and Nimasow, G (2019) Species distribution modeling of tea (Camellia sinensis) in Lohit district of Arunachal Pradesh, India. Int J Ecol Environ 45, 333344.Google Scholar
Pouteau, R, Meyer, JY, Blanchard, P, et al. (2016) Fern species richness and abundance are indicators of climate change on high-elevation islands: evidence from an elevational gradient on Tahiti (French Polynesia). Climatic Change 1, 143156.CrossRefGoogle Scholar
Pownitha, KV, Nagaraja, HPB, Charles, B, Vasudeva, R, Aravind, NA and Ravikanth, G (2022) Ecological niche modelling to identify suitable sites for cultivation of two important medicinal lianas of the Western Ghats, India. Tropical Ecology 63(3), 423432.Google Scholar
Qi, F, Wei, L, Yansui, L, et al. (2004) Impact of desertification and global warming on soil carbon in northern China. Journal of Geophysical Research, [Atmospheres] 109, D02104.Google Scholar
Raina, AP, Abraham, Z and Sivaraj, N (2015) Diversity analysis of Kaempferia galanga L. germplasm from South India using DIVA-GIS approach. Industrial Crops and Products 69, 433439.CrossRefGoogle Scholar
Ray, D, Behera, MD and Jacob, J (2014) Indian Brahmaputra valley offers significant potential for cultivation of rubber trees under changed climate. Current Science 10, 461469.Google Scholar
Roy, PS, Meiyappan, P, Joshi, PK, et al. (2016) Decadal land use and land cover classifications across India, 1985, 1995, 2005. Oak Ridge, Tennessee: ORNL DAAC.Google Scholar
Sarma, RR, Munsi, M and Ananthram, AN (2015) Effect of climate change on invasion risk of giant African snail (Achatina fulica Férussac, 1821: Achatinidae) in India. PLoS One 10, e0143724.CrossRefGoogle ScholarPubMed
Sen, S, Gode, A, Ramanujam, S, et al. (2016) Modeling the impact of climate change on wild Piper nigrum (Black Pepper) in Western Ghats, India using ecological niche models. J Plant Res 129, 10331040.CrossRefGoogle ScholarPubMed
Sharpe, JM (2019) Fern ecology and climate change. Indian Fern J 36, 179199.Google Scholar
Sharpe, JM, Mehltreter, K and Walker, LR (2010) Ecological Importance of Ferns. In Mehltreter, K, Walker, LR and Sharpe, JM (eds), Fern Ecology. Cambridge: Cambridge University Press.Google Scholar
Shrestha, N and Zhang, XC (2015) Is Huperzia hamiltonii (Spreng.) Trevis. a Himalayan endemic? An empirical evaluation using species distribution modeling. Indian Fern J 31, 154161.Google Scholar
Sony, RK, Sen, S, Kumar, S, et al. (2018) Niche models inform the effects of climate change on the endangered Nilgiri Tahr (Nilgiritragus hylocrius) populations in the southern Western Ghats, India. Ecological Engineering 1, 355363.CrossRefGoogle Scholar
Sreekumar, ER and Nameer, PO (2021) Impact of climate change on two high-altitude restricted and endemic flycatchers of the Western Ghats, India. Current Science 121, 1335.CrossRefGoogle Scholar
Sreekumar, ER and Nameer, PO (2022) A MaxEnt modelling approach to understand the climate change effects on the distributional range of White-bellied Sholakili Sholicola albiventris (Blanford, 1868) in the Western Ghats, India. Ecol 70, 101702.Google Scholar
Sreekumar, VB, Suganthasakthivel, R, Sreejith, KA, et al. (2016) Predictive distribution modelling of Calamus andamanicus Kurz, an Endemic Rattan from Andaman and Nicobar Islands, India. J For Environ Sci 32, 94–8.Google Scholar
Syfert, MM, Brummitt, NA, Coomes, DA, et al. (2018) Inferring diversity patterns along an elevation gradient from stacked SDMs: a case study on Mesoamerican ferns. Glob Ecol Conserv 16, e00433.Google Scholar
Thakur, KK, Bhat, P, Kumar, A, Ravikanth, G and Saikia, P (2022) Distribution mapping of Bauhinia vahlii Wight & Arn. in India using ecological niche modelling. Tropical Ecology 63(2), 286299.CrossRefGoogle Scholar
Walker, LR (1994) Effects of fern thickets on woodland development on landslides in Puerto Rico. Journal of Vegetation Science 5, 525532.CrossRefGoogle Scholar
Walker, LR, Mehltretter, K and Sharpe, JM (2010) Current and future directions in fern ecology. In Mehltretter, K Walker, LR and Sharpe, JM (eds), Fern Ecology. Cambridge: Cambridge University Press.Google Scholar
Walker, LR and Sharpe, JM (2010) Ferns, disturbance and succession. In Mehltretter, K Walker, LR and Sharpe, JM (eds), Fern Ecology. Cambridge: Cambridge University Press.Google Scholar
Wang, CJ, Wan, JZ, Zhang, ZX, et al. (2016) Identifying appropriate protected areas for endangered fern species under climate change. SpringerPlus 5, 112.Google ScholarPubMed
Wanga, WC, Lob, NJ, Changc, WI, et al. (2012) Modeling spatial distribution of a rare and endangered plant species (Brainea insignis) in central Taiwan. International archives of the photogrammetry, remote. Sensing and Spatial Information Sciences 39, 241246.Google Scholar
Williams, JN, Seo, C, Thorne, J, et al. (2009) Using species distribution models to predict new occurrences for rare plants. Diversity and Distributions 15, 565576.CrossRefGoogle Scholar
Yang, J, Huang, Y, Jiang, X, et al. (2022) Potential geographical distribution of the endangered plant Isoetes under human activities using MaxEnt and GARP. Global Ecology and Conservation 38, e02186.CrossRefGoogle Scholar
Zurell, D, Franklin, J, König, C, et al. (2020) A standard protocol for reporting species distribution models. Ecography 43, 12611277.CrossRefGoogle Scholar
Figure 0

Figure 1. The background map generated based on the evergreen forest patches in Southern Western Ghats (Indian Biodiversity Information System https://www.indiaobservatory.org.in/tool/ibis) showing the distribution locations of Elaphoglossum beddomei in Southern Western Ghats (yellow dots); predicted potential habitat of E. beddomei in current climatic regime (dark blue regions); the background with existing evergreen forest patches (light blue regions).

Figure 1

Table 1. Contribution of selected bioclimatic variables to the distribution of E. beddomei in current climatic regime

Figure 2

Table 2. Habitat loss and gain in 2041–2070 time period

Figure 3

Figure 2. Habitat gain-unchanged-loss map of E. beddomei in 2040–2071; a. SSP126 scenario and b. SSP585 scenario – black (1) indicated habitat gain; blue (0) indicated unchanged habitat; and red (–1) indicated habitat loss.

Supplementary material: File

Thulasi et al. supplementary material

Thulasi et al. supplementary material
Download Thulasi et al. supplementary material(File)
File 12 KB