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Bats in a cave tourism and pilgrimage site in eastern India: conservation challenges

Published online by Cambridge University Press:  25 November 2020

Subrat Debata*
Affiliation:
Department of Biodiversity and Conservation of Natural Resources, Central University of Orissa, Koraput764021, Odisha, India, and Aranya Foundation, Panchasakha Nagar, Dumduma, Bhubaneswar, Odisha, India
*
(Corresponding author) E-mail subrat.debata007@gmail.com

Abstract

Caves and other subterranean habitats are crucial for the survival of many bat species, but often deteriorate as a result of visits by tourists. The aim of the study was to understand the conservation challenges associated with the cave dwelling bats at Gupteswar cave tourism and pilgrimage site in eastern India and to develop conservation recommendations. I counted bat populations and monitored tourist visits once per month for 12 months during September 2016–August 2017. Roosting and breeding activities of eight species of bats, including two nationally threatened species, were recorded from five caves. The number of bats counted during the 12 survey days was 785–940 individuals. Tourism activity occurred throughout the year but was higher during local festive seasons; the maximum number of tourist entries recorded in a single day was 2,769. Installation of gated entrances, scheduling of visits to control overcrowding, restriction of access to caves with maternity colonies during breeding seasons, and minimal use of electric bulbs for illumination would minimize disturbance to the bats. Installation of educational display boards would help to create awareness of the conservation importance of bats amongst the cave visitors.

Type
Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press on behalf of Fauna & Flora International

Introduction

Nature-based tourism expresses the relationship between nature and society, and the sustainability of such tourism is largely dependent upon ecosystem services such as provisioning, regulation and cultural services (Pueyo-Ros, Reference Pueyo-Ros2018). Cave tourism makes an estimated contribution of USD 100 million annually to the global economy (Cigna & Forti, Reference Cigna and Forti2013) and brings direct benefits to local communities (Pennisi et al., Reference Pennisi, Holland and Stein2004; Cousins & Compton, Reference Cousins and Compton2005). However, poorly managed tourism can pose significant threats to cave biodiversity by negatively affecting cave habitats and microclimates (Mann et al., Reference Mann, Steidl and Dalton2002; Paksuz & Özkan, Reference Paksuz and Özkan2012), for which cave dwelling organisms such as bats have specific requirements (IUCN SSC, 2014). Bats are one of the most abundant and widely distributed mammalian groups; they provide services such as pollination, seed dispersal, insect pest control, and distribute materials and nutrients (Boyles et al., Reference Boyles, Cryan, Mccracken and Kunz2011; Kunz et al., Reference Kunz, Torrenz, Bauer and Lobova2011), and are essential for maintaining cave biodiversity (Deharveng & Bedos, Reference Deharveng, Bedos, White and Culver2012). As cave ecosystems are inherently devoid of primary productivity, bat guano provides organic input that supports the survival of endemic and highly specialized cave fauna whose life cycles depend upon the nutrients from guano (Fenolio et al., Reference Fenolio, Graening, Collier and Stout2006; Deharveng & Bedos, Reference Deharveng, Bedos, White and Culver2012). Many nectarivorous bats inhabiting caves in fragmented habitats are the most important pollinators of various agricultural crops (Sritongchuay et al., Reference Sritongchuay, Kremen and Bumrungsri2016). Unfortunately, populations of many bat species, including cave dwelling species, are threatened by loss and degradation of habitat, hunting, persecution, emerging diseases and climate change (Meyer et al., Reference Meyer, Aguiar, Aguirre, Baumgarten, Clarke and Cosson2010). Of these, habitat loss and degradation are the greatest threats to bats over most of their range (Mickleburgh et al., Reference Mickleburgh, Hutson and Racey2002; Racey & Entwistle, Reference Racey, Entwistle, Kunz and Fenton2003; Jones et al., Reference Jones, Jacobs, Kunz, Willig and Racey2009; Kingston, Reference Kingston2010; Meyer et al., Reference Meyer, Aguiar, Aguirre, Baumgarten, Clarke and Cosson2010).

Globally, c. 449 species of bats prefer caves and other subterranean habitats (Luo et al., Reference Luo, Jiang, Lu, Wang, Wang and Feng2013) for roosting, hibernating, mating, aggregating and raising their young (Kunz, Reference Kunz and Kunz1982; Hutson et al., Reference Hutson, Mickleburgh and Racey2001; Kunz & Lumsden, Reference Kunz, Lumsden, Kunz and Fenton2003; Murray & Kunz, Reference Murray, Kunz, Culver and White2005). Preference of bats for such places depends on the characteristics and quality of the habitat (Murray & Kunz, Reference Murray, Kunz, Culver and White2005; Struebig et al., Reference Struebig, Kingston, Zubaid, Le Comber, Mohd-Adnan and Turner2009; Phelps et al., Reference Phelps, Jose, Labonite and Kingston2016). Human activities such as caving, tourism, guano harvesting and other deliberate or accidental disturbances in and around roosting caves put negative pressure on bats and cause declines (Özgül et al., Reference Özgül, Bilgin, Furman and Woloszyn2000; Furman & Özgül, Reference Furman and Özgül2002, Reference Furman and Özgül2004; Papadatou et al., Reference Papadatou, Butlin, Pradel and Altringham2009; Luo et al., Reference Luo, Jiang, Lu, Wang, Wang and Feng2013; IUCN SSC, 2014). Protection of caves can contribute to the conservation of bats and other cave dwelling organisms (Niu et al., Reference Niu, Wang, Zhao and Liu2007; Paksuz & Özkan, Reference Paksuz and Özkan2012; Luo et al., Reference Luo, Jiang, Lu, Wang, Wang and Feng2013). There is increasing interest from government agencies, academics, NGOs and corporate agencies in conservation of cave dwelling bats (Bat Conservation International, 2013; Furey & Racey, Reference Furey, Racey, Voigt and Kingston2016). For example, human activities have been regulated and roosting sites have been protected from disturbance in Turkey (Paksuz & Özkan, Reference Paksuz and Özkan2012), USA (Richter et al., Reference Richter, Humphrey, Cope and Brack1993; Martin et al., Reference Martin, Leslie, Payton, Puckette and Hensley2003) and Spain (Alcalde et al., Reference Alcalde, Artácoz and Meijide2012). Many organizations have developed guidelines for protection of cave roosts (Sheffield et al., Reference Sheffield, Shaw, Heidt and Mcclenaghan1992), and conservation codes for cave visitors (Hutson et al., Reference Hutson, Mickleburgh and Mitchell-Jones1988) and guano harvesters (IUCN SSC, 2014).

Nevertheless, information about the location of caves and the species they support, population estimates, local threats and conservation activities remains insufficient in most tropical regions, particularly in Asia. Information is needed to identify areas with the highest conservation needs (Furey & Racey, Reference Furey, Racey, Voigt and Kingston2016; Tanalgo et al., Reference Tanalgo, Tabora and Hughes2018). In India, human disturbance and artificial illumination in cave tourism sites are known to have caused the decline of the bat population in Borra cave in southern India (Srinivasulu & Srinivasulu, Reference Srinivasulu and Srinivasulu2003) and Kotumsar and Dandak caves in central India (Biswas et al., Reference Biswas, Shrotriya, Rajput and Sasmal2011). Here I make recommendations for conservation of bats inhabiting Gupteswar cave tourism and pilgrim site in eastern India. I gathered information on the seasonal abundance and reproductive phenology of bat species and on tourism activity. I also evaluated the knowledge and attitudes of local people and tourists towards bats inhabiting the caves.

Study area

Gupteswar cave tourism and pilgrimage site (Fig. 1) lies in the Koraput district of Odisha state, eastern India, adjoining Kanger Valley National Park of neighbouring Chhattisgarh state. The area is within the riparian zone of Gupteswar reserve forest, which is tropical mixed deciduous vegetation (Champion & Seth, Reference Champion and Seth1968). Such habitats are often characterized by a highly heterogeneous vegetation structure with multiple layers of stratification, providing a wide range of foraging niches for bats (Struebig et al., Reference Struebig, Kingston, Zubaid, Mohd-Adnan and Rossiter2008). The area receives a mean annual rainfall of 1,522 mm and temperature varies from a minimum of 12 °C during winter (January) to a maximum of 38 °C in summer (May). There are five multi-chambered and multi-entrance limestone caves (Fig. 1b; Gupteswar, Swargadwara, Parabhadi 1, Parabhadi 2 and Dhabaleswar), within 80–295 m of each other. Gupteswar and Swargadwara are illuminated with electric bulbs throughout the day and night. All five caves have sacred importance for the local villagers and therefore are major pilgrim and tourism sites. Tourists visit from both nearby areas and neighbouring states. Hunting and persecution of bats in the caves are strictly prohibited by the local people because of the associated sacred beliefs.

Fig. 1 (a) Gupteswar cave tourism and pilgrimage site in eastern India, showing the location of individual caves, villages, tourist rest houses and roads. The Saberi River acts as the boundary between the states of Odisha and Chhattisgarh. (b) The caves, showing the entrances and bat roosting and breeding sites. Cave openings without arrows are situated at a higher elevation and are not used as entrances.

Methods

Bat surveys

The study was carried out over 12 months during September 2016–August 2017, with field support from local people and volunteers. Surveys were on 2 consecutive days in each month. Estimation of the abundance of bats in each cave and investigation of their reproductive phenology was carried out on the first day, and monitoring of visits and assessment of people's knowledge of and attitude towards bat conservation were carried out on the second day.

In areas of the caves used for roosting, I captured bats using a scoop net, mounted on an extendable rod when required, recorded morphological measurements and characters for identification, and released the bats immediately afterwards. Species were identified using Bates & Harrison (Reference Bates and Harrison1997) and Srinivasulu et al. (Reference Srinivasulu, Racey and Mistry2010). I examined the reproductive status of all captured bats, following Racey (Reference Racey, Kunz and Parsons2009). Care was taken to avoid harming the bats, following the protocols described by Mitchell-Jones & McLeish (Reference Mitchell-Jones and Mcleish2004). No voucher specimens were collected. I used the direct roost count method (Thomas & Laval, Reference Thomas, Laval and Kunz1988) for counting the total number of bats in each cave. For this, I divided each cave into sections and systematically counted the number of individual bats roosting, using a spotlight to ensure no areas were missed and there was no double counting. Counting of bats was early in the morning, prior to capturing them and when they were less active and there were no visiting tourists. As I was unable to identify and count all of the individual roosting bats there may have been unintended biases in the counts. As it is difficult to identify bat species without capture, the total counts of bats in each cave were categorized by family only.

Visitation

Visitation was monitored by counting the number of groups and individuals visiting the caves. A volunteer assigned to each cave monitored tourists during 7.00–17.00 on each survey day, with a total effort of 600 hours of monitoring throughout the caves during the study period. The number of people in each group and their time of entry into the cave was recorded. The appearance of one person in each group was memorized, so that their group's exit time could be recorded and thus the time spent by that group in the cave calculated. If a group comprising N individuals visited n caves, I considered the total number of individual entries to be N × n. Activities of the visitors inside the caves were also monitored and noted.

Knowledge and attitudes

Using a semi structured questionnaire (Supplementary Material 1) I opportunistically interviewed people visiting the cave complex, if they were willing to be interviewed, to examine their knowledge of bats and their attitudes towards their conservation. Conway et al. (Reference Conway, Hernandez, Carroll, Green and Larson2015) and Debata et al. (Reference Debata, Swain, Sahu and Palei2016a) used a similar non-random selection of subjects for attitude surveys. The questionnaire included five statements (Table 1) that examined the knowledge of respondents on ecological importance, habitats and threats, and their views regarding the conservation importance of cave dwelling bats. The interview was in Odia, the local language, or in Hindi, depending on a respondent's preference. Based on the answer to the statement ‘Bats and their roosting sites should be protected in cave tourism sites’, attitudes towards bat conservation were broadly categorized as aesthetic (concerned with the physical attractiveness and symbolic appeal of animals), moralistic (strong opposition to presumed cruelty towards animals), eco-scientific (aware of the ecological importance of bats) or negative (fear, dislike, or indifference towards bats and their conservation), following Kellert & Wilson (Reference Kellert, Wilson, Kellert and Wilson1993).

Table 1 Comparison of knowledge on bats and attitude towards their conservation among 366 tourists and 76 local people visiting Gupteswar cave tourism and pilgrimage site (Fig. 1) during September 2016–August 2017. Per cent calculations are row-wise.

Data analysis

I used a one-way ANOVA to examine any differences in abundance of bats between months and seasons, the correlation coefficient to investigate the effect of tourist visitation on the abundance of bats, and the Student's t test to compare visits between festive and non-festive periods.

Results

Species richness and abundance of bats

During the entire study period I captured, and released, 140 individual bats of eight species in the five caves: Rhinolophus lepidus, Rhinolophus rouxii, Hipposideros ater, Hipposideros galeritus, Hipposideros speoris, Megaderma lyra, Megaderma spasma and Taphozous melanopogon. Five species (R. lepidus, H. ater, H. galeritus, H. speoris, T. melanopogon) were recorded in Swargadwara cave, four (R. lepidus, H. galeritus, M. lyra, T. melanopogon) in Parabhadi cave 1, three (R. lepidus, R. rouxii, H. galeritus) in Gupteswar cave, two (R. lepidus, M. spasma) in Dhabaleswar cave, and one (M. lyra) in Parabhadi cave 2. The total number of bats counted on each survey day (all caves and species combined; Table 2) did not vary significantly between months (F = 0.02, df = 11, 48, P > 0.05) or seasons (summer, monsoon and winter; F = 0.49, df = 2, 12, P > 0.05). The number of bats counted on each survey day and in each cave are provided in Supplementary Table 1.

Table 2 Mean ± SD total number of bats counted per day during the 12 survey days in the five caves at Gupteswar cave tourism and pilgrimage site (Fig. 1) during September 2016–August 2017.

Reproductive phenology

Of the eight species, breeding of five species (R. lepidus, H. ater, H. galeritus, M. lyra and T. melanopogon) was recorded, during February–July (Fig. 2). Pregnancy in R. lepidus was first observed during February–April and females carrying non-volant pups were recorded during April–June. Pregnancy was observed in H. ater and H. galeritus during February and females carrying non-volant pups were recorded during April and June–July. Pregnancy in M. lyra was observed during March–April and females carrying non-volant pups were recorded during May and July. Pregnancy in T. melanopogon was observed during February–April and females carrying non-volant pups were recorded during April–July.

Fig. 2 (a) Reproductive phenology (numbers of females pregnant and with pups) amongst the 140 bats captured, and (b) number of visitors at Gupteswar cave tourism and pilgrimage site (Fig. 1), during September 2016–August 2017.

Visitation

A total 15,942 visitor in 1,248 groups (Group size range 1–88; mean 12.77 ± SD 8.67) were recorded (Table 3). Groups comprising 1–15 people were most frequent (73% of all visits), followed by 16–30 people (25%), 31–45 people (1.5%) and > 45 people (0.5%). On average each cave was visited by 3,188.4 ± SD 326.6 individual tourists during the 12 survey days. Visits were significantly higher during local cultural festivals associated with the caves, during February–July (t = 2.66. df = 6, P < 0.05; Fig. 2), coinciding with the reproductive period of R. lepidus, H. ater, H. galeritus, M. lyra and T. melanopogon. The overall monthly bat count was not correlated with number of visitors (r = −0.29, df = 10, P > 0.05).

Table 3 Number of tourists who visited the five caves at Gupteswar cave tourism and pilgrim site (Fig. 1) in each survey day during September 2016–August 2017. Values in parentheses are the number of tourist groups. The monthly totals are presented in Fig. 2b.

Each tourist group spent a mean of 15.7 ± SD 9.4 minutes in the caves. The duration of cave visits by tourists was positively correlated with visitor group size (r = 0.53, df = 34, P < 0.01). The mean time spent by tourists inside each cave was highest (1.86 minutes) in Gupteswar, followed by Swargadwara (1.77), Parabhadi 1 (0.88), Parabhadi 2 (0.77) and Dhabaleswar (0.67). The activities of tourists inside the caves included religious and spiritual practices, photography and talking. The main purpose of the visits were cultural (317 respondents) and for leisure (49).

Knowledge and attitudes

A total of 76 local villagers and 366 tourists were interviewed. Information on their responses and demographic profiles are given in Table 1 and Table 4, respectively. Nearly 86% of respondents were not aware that bats are mammals, with 79% (62% of tourists and 93% of local people) indicating they are birds. Only 23% (27% of tourists and one local person) were aware that bats are ecologically important as controllers of insect pests, and 77% of the respondents believed bats are a nuisance, feeding in the fruit orchards and home gardens. Sixty-four per cent of all respondents (58% of tourists and 91% of local people) agreed that caves are important habitat for bats. Amongst all the respondents, only 11% agreed that human activities inside caves are a threat to bats, and 80% of respondents (78% of tourists and 89% of local people) claimed they never teased or harmed bats. Regarding the conservation of bats at Gupteswar, all the local people but only 32% of the tourists agreed that bats and their roosting sites should be protected and their attitude was mostly aesthetic (55%) followed by moralistic (24%) and eco-scientific (21%). However, 68% of the tourists had a negative attitude towards the conservation of bats in caves because of the guano and the smell.

Table 4 Demographic characteristics of the local people (n = 76) and tourists (n = 366) interviewed to assess their knowledge and attitude towards bats at Gupteswar cave tourism and pilgrim site, eastern India, during September 2016–August 2017.

Discussion

Cave tourism is becoming increasingly popular as people are motivated to visit caves for their inherent natural landscape features (Okonkwo et al., Reference Okonkwo, Afoma and Martha2017). The limestone Gupteswar caves lie within natural forest and, being associated with sacred values and accessible by road, attract tourists throughout the year. The assemblage of bats in caves is governed by two main factors; surface level disturbance, including anthropogenic activities and availability of forest, and the complexity of the caves, including availability of roosting sites, structural heterogeneity and number of entrances (Phelps et al., Reference Phelps, Jose, Labonite and Kingston2016). Gupteswar caves support at least eight species of bats, comprising 32% of the 25 species known in Odisha state (Debata et al., Reference Debata, Palita and Behera2016b).

Cave dwelling bats are often hunted for their meat and for medicinal uses (da Costa Rego et al., Reference da Costa Rego, Zeppelini, Lopez and Alves2015; Tanalgo et al., Reference Tanalgo, Teves, Salvana, Baleva and Tabora2016), but bats inhabiting sacred caves may benefit from local customary regulations and taboos (Metcalfe et al., Reference Metcalfe, Ffrench-Constant and Gordon2010; Golden & Comaroff, Reference Golden and Comaroff2015; Furey & Racey, Reference Furey, Racey, Voigt and Kingston2016; Fernandez-Llamazares et al., Reference Fernandez-Llamazares, Lopez-Baucells, Rocha, Andriamitandrina, Andriatafika and Burgas2018). Although bats roosting in the Gupteswar caves are not harmed, because of sacred beliefs associated with the caves, unregulated tourism activities inside the caves are a potential threat to the bats. As part of the development of any cave for tourism, structural modification and introduction of artificial lighting is a common intervention (Furey & Racey, Reference Furey, Racey, Voigt and Kingston2016), including at Gupteswar. Tourists visit the Gupteswar caves throughout the year, and spend more time in Gupteswar and Swargadwara, which are only artificially illuminated. Larger tourist groups spent more time inside the caves and explored more areas within the caves, increasing the likelihood of approaching close to areas with roosting sites and maternity colonies. Anthropogenic disturbance from artificial illumination, noise and human activities increase alertness in bats, leading to increases in flight activity, vocalization intensity and energy expenditure (Song et al., Reference Song, Wei and Liang2000; Mann et al., Reference Mann, Steidl and Dalton2002; Cardiff et al., Reference Cardiff, Ratrimomanarivo and Goodman2012). Structural modification and artificial lighting can weaken the ability to avoid obstacles during flight, and affect roost use pattern, emergence time, and growth and development of juveniles (Srinivasulu & Srinivasulu, Reference Srinivasulu and Srinivasulu2003; Boldogh et al., Reference Boldogh, Dobrosi and Samu2007; McGuire & Fenton, Reference Mcguire and Fenton2010). Human activities can also cause marked fluctuations in microclimatic condition of the caves by altering the temperature, relative humidity and carbon dioxide concentration (Pulido-Bosch et al., Reference Pulido-Bosch, Martin-Rosales, López-Chicano, Rodriguez-Navarro and Vallejos1997; Gunn, Reference Gunn2004), the requirements for which are specific to individual bat species. Disturbances in breeding and maternity colonies can also cause adults to drop their young, from stress, and it is difficult for the young to be retrieved (Sheffield et al., Reference Sheffield, Shaw, Heidt and Mcclenaghan1992; Petit et al., Reference Petit, Rojer and Pors2006). At Gupteswar caves visitation was highest during the reproductive period of several of the bat species present. Similarly, in Cambodia the time of year with greatest visitation to caves coincided with the breeding of several cave dwelling insectivorous bats (Lim et al., Reference Lim, Cappelle, Hoem and Furey2018).

A study using an index of bat cave vulnerability revealed that caves with high species diversity are more vulnerable to anthropogenic activities than caves with low species diversity (Tanalgo et al., Reference Tanalgo, Tabora and Hughes2018). At Gupteswar, tourism related human disturbance is the major threat to bats; without appropriate management the bat populations may potentially decline or abandon these caves. Protection of roosting sites from anthropogenic disturbances should be an essential component of any conservation strategy (Furey & Racey, Reference Furey, Racey, Voigt and Kingston2016). In India, however, there are no laws or guidelines to protect and conserve caves and their biodiversity (Walker & Molur, Reference Walker and Molur2003; Biswas, Reference Biswas2016). Bats inhabiting caves opened for tourism may be persecuted, as in Borra cave in southern India (author, pers. obs.). Although none of the bats at Gupteswar appear to be harmed, because of the sacred beliefs associated with the caves, the uncontrolled human disturbance is a major challenge. Installation of gates at entry points and scheduling of visits to control overcrowding are required, and illumination inside the cave system should be turned off at night, when there are no visitors and during non-visiting daylight hours. The areas of the caves used as maternity colonies (Fig. 1b) should not be open for visitation during breeding seasons. Such initiatives have, for example, proved effective at a cave in the Rocky Mountains of Canada (Olson et al., Reference Olson, Hobson and Pybus2011) and at the Dupnisa cave system in Turkey (Paksuz & Özkan, Reference Paksuz and Özkan2012). However, prior to installation of any gates it is important to understand the ecology and behaviour of the bat species present, as poorly designed and improperly placed gates can be detrimental to bats (Ludlow & Gore, Reference Ludlow and Gore2000; Pugh & Altringham, Reference Pugh and Altringham2005; Alcalde et al., Reference Alcalde, Artácoz and Meijide2012). Sharing of knowledge regarding the importance of bats can help to improve attitudes towards them and make people more aware of the species’ conservation needs (Pennisi & Confer, Reference Pennisi, Confer, Delamere, Randall and Robinson2005; Trewhella et al., Reference Trewhella, Rodriguez-Clark, Corp, Entwistle, Garrett and Granek2005; Kingston, Reference Kingston, Voigt and Kingston2016; García-Cegarra & Pacheco, Reference García-Cegarra and Pacheco2017). Bat watching has become a popular recreational activity in some European countries (Pennisi et al., Reference Pennisi, Holland and Stein2004). Educational display boards on the conservation importance of cave dwelling bats have already been installed at the entry area of each cave at Gupteswar, to sensitize visitors. In addition, long-term monitoring of the behaviour and population dynamics of the bats of the Gupteswar cave system is required, in particular in relation to tourism activities.

Acknowledgements

This study was carried out with financial support from Bat Conservation International, Austin, USA. I thank the Principal Chief Conservator of Forest and Chief Wildlife Warden, Odisha, for providing permission to carry out the study; T. Kar, S.K. Jena, S. Nanda, A.K. Das, S. Purohit, K.T. Samal and the local villagers for their generous help; H.S. Palei for developing the study area map; and the reviewers for their valuable suggestions.

Conflicts of interest

None.

Ethical standards

Interviews followed the ethical guidelines of the Indian Council of Medial Research, India (Mathur, Reference Mathur2017), and this research otherwise abided by the Oryx guidelines on ethical standards.

Footnotes

Supplementary material for this article is available at doi.org/10.1017/S003060531900098X

References

Alcalde, J.T., Artácoz, A. & Meijide, F. (2012) Recovery of a colony of Miniopterus schreibersii from a cave, Cueva de Ágreda, in Soria. Barbastella, 5, 3235.Google Scholar
Bat Conservation International (2013) A Five-Year Strategy for Global Bat Conservation. Bat Conservation International, Austin, USA.Google Scholar
Bates, P.J.J. & Harrison, D.L. (1997) Bats of the Indian Subcontinent. Harrison Zoological Museum, Sevenoaks, UK.Google Scholar
Biswas, J. (2016) Caving in. downtoearth.org.in/news/environment/caving-in-52339 [accessed 15 March 2019].Google Scholar
Biswas, J., Shrotriya, S., Rajput, Y. & Sasmal, S. (2011) Impacts of ecotourism on bat habitats in caves of Kanger Valley National Park, India. Research Journal of Environmental Sciences, 5, 752762.CrossRefGoogle Scholar
Boldogh, S., Dobrosi, D. & Samu, P. (2007) The effects of the illumination of buildings on house-dwelling bats and its conservation consequences. Acta Chiropterologica, 9, 527534.CrossRefGoogle Scholar
Boyles, J.G., Cryan, P.M., Mccracken, G.F. & Kunz, T.H. (2011) Economic importance of bats in agriculture. Science, 332, 4142.CrossRefGoogle ScholarPubMed
Cardiff, S.G., Ratrimomanarivo, F.H. & Goodman, S.M. (2012) The effect of tourist visits on the behavior of Rousettus madagascariensis (Chiroptera: Pteropodidae) in the caves of Ankarana, northern Madagascar. Acta Chiropterologica, 14, 479490.Google Scholar
Champion, H.G. & Seth, S.K. (1968) The Forest Types of India. Government of India Press, Nasik, India.Google Scholar
Cigna, A.A. & Forti, P. (2013) Caves: the most important geotouristic feature in the world. Tourism and Karst Areas, 6, 926.Google Scholar
Conway, A.L., Hernandez, S.A., Carroll, J.P., Green, G.T. & Larson, L. (2015) Local awareness of and attitudes towards the pygmy hippopotamus Choeropsis liberiensis in the Moa River Island Complex, Sierra Leone. Oryx, 49, 550558.CrossRefGoogle Scholar
Cousins, J.A. & Compton, S.G. (2005) The Tongan flying fox Pteropus tonganus: status, public attitudes and conservation in the Cook Islands. Oryx, 39, 196203.CrossRefGoogle Scholar
da Costa Rego, K.M., Zeppelini, C.G., Lopez, L.C.S. & Alves, R.R.N. (2015) Assessing human–bat interactions around a protected area in northeastern Brazil. Journal of Ethnobiology and Ethnomedicine, 11, 80.CrossRefGoogle Scholar
Debata, S., Swain, K.K., Sahu, H.K. & Palei, H.S. (2016a) Human–sloth bear conflict in a human-dominated landscape of northern Odisha, India. Ursus, 27, 9098.CrossRefGoogle Scholar
Debata, S., Palita, S.K. & Behera, S. (2016b) Bats of Odisha—A Pictorial Hand Book. Odisha Biodiversity Board, Bhubaneswar, Odisha, India.Google Scholar
Deharveng, L. & Bedos, A. (2012) Diversity patterns in the tropics. In Encyclopedia of Caves (eds White, W.B. & Culver, D.C.), pp. 238250. Academic Press, Chennai, India.CrossRefGoogle Scholar
Fenolio, D.B, Graening, G.O, Collier, B.A. & Stout, J.F. (2006) Coprophagy in a cave-adapted salamander; the importance of bat guano examined through nutritional and stable isotope analyses. Proceedings of the Royal Society B, 273, 439443.CrossRefGoogle Scholar
Fernandez-Llamazares, A., Lopez-Baucells, A., Rocha, R., Andriamitandrina, S.F.M., Andriatafika, Z.E., Burgas, D. et al. (2018) Are sacred caves still safe havens for the endemic bats of Madagascar? Oryx, 52, 271–275.CrossRefGoogle Scholar
Furey, N.M. & Racey, P.A. (2016) Conservation ecology of cave bats. In Bats in the Anthropocene: Conservation of Bats in a Changing World (eds Voigt, C.C. & Kingston, T.), pp. 463500. Springer, Cham, Switzerland.CrossRefGoogle Scholar
Furman, A. & Özgül, A. (2002) The distribution of cave-dwelling bats and conservation status of underground habitats in Istanbul area. Ecological Research, 17, 6977.CrossRefGoogle Scholar
Furman, A. & Özgül, A. (2004) The distribution of cave-dwelling bats and conservation status of underground habitats in northwestern Turkey. Biological Conservation, 120, 247252.CrossRefGoogle Scholar
García-Cegarra, A.M. & Pacheco, A.S. (2017) Whale-watching trips in Peru lead to increases in tourist knowledge, pro-conservation intentions and tourist concern for the impacts of whale-watching on humpback whales. Aquatic Conservation: Marine and Freshwater Ecosystems, 27, 10111020.CrossRefGoogle Scholar
Golden, C.D. & Comaroff, J. (2015) The human health and conservation relevance of food taboos in northeastern Madagascar. Ecology and Society, 20, 42.CrossRefGoogle Scholar
Gunn, J. (ed.) (2004) Encyclopedia of Caves and Karst Science. Routledge, New York, USA.CrossRefGoogle Scholar
Hutson, A.M., Mickleburgh, S.P. & Mitchell-Jones, A.J. (1988) Bats Underground, a Conservation Code. Fauna and Flora Preservation Society, Cambridge, UK, Nature Conservancy Council, Peterborough, UK and the Vincent Wildlife Trust, Ledbury, UK.Google Scholar
Hutson, A.M., Mickleburgh, S.P. & Racey, P.A. (comp.) (2001) Microchiropteran Bats: Global Status Survey and Conservation Action Plan. IUCN/SSC Chiroptera Specialist Group. IUCN, Gland, Switzerland and Cambridge, UK.CrossRefGoogle Scholar
IUCN SSC (2014) IUCN SSC Guidelines for Minimizing the Negative Impact to Bats and Other Cave Organisms from Guano Harvesting. Version 1.0. IUCN, Gland, Switzerland.Google Scholar
Jones, G., Jacobs, D., Kunz, T., Willig, M. & Racey, P. (2009) Carpe noctem: the importance of bats as bioindicators. Endangered Species Research, 8, 93115.CrossRefGoogle Scholar
Kellert, S.R. & Wilson, E.O. (1993) The biological basis of human values of nature. In The Biophilia Hypothesis (eds Kellert, S.R. & Wilson, E.O.), pp. 4267. Island Press, Washington, DC, USA.Google Scholar
Kingston, T. (2010) Research priorities for bat conservation in Southeast Asia: a consensus approach. Biodiversity and Conservation, 19, 471484.CrossRefGoogle Scholar
Kingston, T. (2016) Cute, Creepy, or Crispy—How values, attitudes, and norms shape human behavior toward bats. In Bats in the Anthropocene: Conservation of Bats in a Changing World (eds Voigt, C.C. & Kingston, T.), pp. 571595. Springer, Cham, Switzerland.CrossRefGoogle Scholar
Kunz, T.H. (1982) Roosting ecology of bats. In Ecology of Bats (ed. Kunz, T.H.), pp. 155. Plenum Press, New York, USA.CrossRefGoogle Scholar
Kunz, T.H. & Lumsden, L.F. (2003) Ecology of cavity and foliage roosting bats. In Bat Ecology (eds Kunz, T.H. & Fenton, M.B.), pp. 389. University of Chicago Press, Chicago, USA.Google Scholar
Kunz, T.H., Torrenz, E.B., Bauer, D. & Lobova, T. (2011) Ecosystem services provided by bats. Annals of the New York Academy of Sciences, 1223, 138.CrossRefGoogle ScholarPubMed
Lim, T., Cappelle, J., Hoem, T. & Furey, N. (2018) Insectivorous bat reproduction and human cave visitation in Cambodia: a perfect conservation storm? PLOS ONE, 13, e0196554.CrossRefGoogle ScholarPubMed
Ludlow, M.E. & Gore, J.A. (2000) Effects of a cave gate on emergence patterns of colonial bats. Wildlife Society Bulletin, 28, 191196.Google Scholar
Luo, J., Jiang, T., Lu, G., Wang, L., Wang, J. & Feng, J. (2013) Bat conservation in China: should protection of subterranean habitats be a priority? Oryx, 47, 526531.CrossRefGoogle Scholar
Mann, S.L., Steidl, R.J. & Dalton, V.M. (2002) Effects of cave tours on breeding Myotis velifer. Journal of Wildlife Management, 66, 618624.CrossRefGoogle Scholar
Martin, K.W., Leslie, D.M., Payton, M.E., Puckette, W.L. & Hensley, S.L. (2003) Internal cave gating for protection of colonies of the Endangered gray bat (Myotis grisescens). Acta Chiropterologica, 5, 143150.CrossRefGoogle Scholar
Mathur, R. (2017) National Ethical Guidelines for Biomedical and Health Research Involving Human Participants. Indian Council of Medical Research, New Delhi, India.Google Scholar
Mcguire, L.P. & Fenton, M.B. (2010) Hitting the wall: light affects the obstacle avoidance ability of free-flying little brown bats (Myotis lucifugus). Acta Chiropterologica, 12, 247250.CrossRefGoogle Scholar
Metcalfe, K., Ffrench-Constant, R. & Gordon, I. (2010) Sacred sites as hotspots for biodiversity: the Three Sisters Cave complex in coastal Kenya. Oryx, 44, 118123.CrossRefGoogle Scholar
Meyer, C.F.J., Aguiar, L.M.S., Aguirre, L.F., Baumgarten, J., Clarke, F.M., Cosson, J.-F. et al. (2010) Long-term monitoring of tropical bats for anthropogenic impact assessment: gauging the statistical power to detect population change. Biological Conservation, 143, 27972807.CrossRefGoogle Scholar
Mickleburgh, S.P., Hutson, A.M. & Racey, P.A. (2002) A review of the global conservation status of bats. Oryx, 36, 1834.CrossRefGoogle Scholar
Mitchell-Jones, A.J. & Mcleish, A.P. (2004) Bat Worker's Manual. 3rd edition. Joint Nature Conservation Committee, Peterborough, UK.Google Scholar
Murray, S.W. & Kunz, T.H. (2005) Bats. In Encyclopedia of Caves (eds Culver, D. & White, W.), pp. 3945. Academic Press, London, UK.Google Scholar
Niu, H., Wang, N., Zhao, L. & Liu, J. (2007) Distribution and underground habitats of cave dwelling bats in China. Animal Conservation, 10, 470477.CrossRefGoogle Scholar
Okonkwo, E.E., Afoma, E. & Martha, I. (2017) Cave tourism and its implications to tourism development in Nigeria: a case study of Agu-Owuru cave in Ezeagu. International Journal of Research in Tourism and Hospitality, 3, 1624.Google Scholar
Olson, C.R., Hobson, D.P. & Pybus, M.J. (2011) Changes in population size of bats at a hibernaculum in Alberta, Canada, in relation to cave disturbance and access restrictions. Northwestern Naturalist, 92, 224230.CrossRefGoogle Scholar
Özgül, A., Bilgin, R. & Furman, A. (2000) Cave-dwelling bats (Mammalia: Chiroptera) of Çatalca-Kocaeli region, north-western Turkey. In Proceedings of the VIIIth European Bat Research Symposium (ed. Woloszyn, B.W.), pp. 191198. Chiropterological Information Center, Krakow, Poland.Google Scholar
Paksuz, S. & Özkan, B. (2012) The protection of the bat community in the Dupnisa Cave System, Turkey, following opening for tourism. Oryx, 46, 130136.CrossRefGoogle Scholar
Papadatou, E., Butlin, R.K., Pradel, R. & Altringham, J.D. (2009) Sex-specific roost movements and population dynamics of the Vulnerable long-fingered bat, Myotis capaccinii. Biological Conservation, 142, 280289.CrossRefGoogle Scholar
Pennisi, L. & Confer, J.C. (2005) Attitudes of urban bat watchers. In Eleventh Canadian Congress on Leisure Research (eds Delamere, T., Randall, C. & Robinson, D.), pp. 469471. Department of Recreation and Tourism Management, Malaspina University College, Nanaimo, Canada.Google Scholar
Pennisi, L.A., Holland, S.M. & Stein, T.V. (2004) Achieving bat conservation through tourism. Journal of Ecotourism, 3, 195207.CrossRefGoogle Scholar
Petit, S., Rojer, A. & Pors, L. (2006) Surveying bats for conservation: the status of cave-dwelling bats on Curaçao from 1993 to 2003. Animal Conservation, 9, 207217.CrossRefGoogle Scholar
Phelps, K., Jose, R., Labonite, M. & Kingston, T. (2016) Correlates of cave-roosting bat diversity as an effective tool to identify priority caves. Biological Conservation, 201, 201209.CrossRefGoogle Scholar
Pueyo-Ros, J. (2018) The role of tourism in the ecosystem services framework. Land, 7, 111.CrossRefGoogle Scholar
Pugh, M. & Altringham, J.D. (2005) The effect of gates on cave entry by swarming bats. Acta Chiropterologica, 7, 293299.CrossRefGoogle Scholar
Pulido-Bosch, A., Martin-Rosales, W., López-Chicano, M., Rodriguez-Navarro, C.M. & Vallejos, A. (1997) Human impact in a tourist karstic cave (Aracena, Spain). Environmental Geology, 31, 142149.CrossRefGoogle Scholar
Racey, P.A. (2009) Reproductive assessment. In Behavioural and Ecological Methods for the Study of Bats (eds Kunz, T.H. & Parsons, S.), pp. 249264. The Johns Hopkins University Press, Baltimore, USA.Google Scholar
Racey, P.A. & Entwistle, A.C. (2003) Conservation ecology of bats. In Bat Ecology (eds Kunz, T.H. & Fenton, M.B.), pp. 680743. University of Chicago Press, Chicago, USA.Google Scholar
Richter, A.R., Humphrey, S.R., Cope, J.B. & Brack, V. Jr. (1993) Modified cave entrances: thermal effect on body mass and resulting decline of endangered Indiana bats (Myotis sodalis). Conservation Biology, 7, 407415.CrossRefGoogle Scholar
Sheffield, S.R., Shaw, J.H., Heidt, G.A. & Mcclenaghan, L.R. (1992) Guidelines for the protection of bat roosts. Journal of Mammalogy, 73, 707710.Google Scholar
Song, L.H., Wei, X.N. & Liang, F.Y. (2000) The influences of cave tourism on CO2 and temperature in Baiyun Cave, Hebei, China. International Journal of Speleology, 29, 7787.CrossRefGoogle Scholar
Srinivasulu, B. & Srinivasulu, C. (2003) Summary of the study on roost site characteristics of bats of Borra Cave in Visakhapatnam District, Andhra Pradesh. BAT NET—CCINSA Newsletter, 4, 35.Google Scholar
Srinivasulu, C., Racey, P.A. & Mistry, S. (2010) A key to the bats (Mammalia: Chiroptera) of South Asia. Journal of Threatened Taxa, 2, 10011076.CrossRefGoogle Scholar
Sritongchuay, T., Kremen, C. & Bumrungsri, S. (2016) Effects of forest and cave proximity on fruit set of tree crops in tropical orchards in Southern Thailand. Journal of Tropical Ecology, 32, 269279.CrossRefGoogle Scholar
Struebig, M.J., Kingston, T., Zubaid, A., Mohd-Adnan, A. & Rossiter, S.J. (2008) Conservation value of forest fragments to Paleotropical bats. Biological Conservation, 141, 21122126.CrossRefGoogle Scholar
Struebig, M.J., Kingston, T., Zubaid, A., Le Comber, S.C., Mohd-Adnan, A., Turner, A. et al. (2009) Conservation importance of limestone karst outcrops for Palaeotropical bats in a fragmented landscape. Biological Conservation, 142, 20892096.CrossRefGoogle Scholar
Tanalgo, K.C., Teves, R.D., Salvana, F.R.P., Baleva, R.E. & Tabora, J.A.G. (2016) Human–bat interactions in caves of south central Mindanao, Philippines. Wildlife Biology in Practice, 12, 114.Google Scholar
Tanalgo, K.C., Tabora, J.A.G. & Hughes, A.C. (2018) Bat cave vulnerability index (BCVI): a holistic rapid assessment tool to identify priorities for effective cave conservation in the tropics. Ecological Indicators, 89, 852860.CrossRefGoogle Scholar
Thomas, D.W. & Laval, R.K. (1988) Survey and census methods. In Ecological and Behavioral Methods for the Study of Bats (ed. Kunz, T.H.), pp. 7789. Smithsonian Institution Press, Washington, DC, USA.Google Scholar
Trewhella, W.J., Rodriguez-Clark, K.M., Corp, N., Entwistle, A., Garrett, S.R.T., Granek, E. et al. (2005) Environmental education as a component of multidisciplinary conservation programs: lessons from the conservation initiatives for Critically Endangered fruit bats in the Western Indian Ocean. Conservation Biology, 19, 7585.CrossRefGoogle Scholar
Walker, S. & Molur, S. (Comp) (2003) Summary of the Status of South Asian Chiroptera. Extracted from CAMP 2002 Report. Zoo Outreach Organisation, CBSG, South Asia and WILD, Coimbatore, India.Google Scholar
Figure 0

Fig. 1 (a) Gupteswar cave tourism and pilgrimage site in eastern India, showing the location of individual caves, villages, tourist rest houses and roads. The Saberi River acts as the boundary between the states of Odisha and Chhattisgarh. (b) The caves, showing the entrances and bat roosting and breeding sites. Cave openings without arrows are situated at a higher elevation and are not used as entrances.

Figure 1

Table 1 Comparison of knowledge on bats and attitude towards their conservation among 366 tourists and 76 local people visiting Gupteswar cave tourism and pilgrimage site (Fig. 1) during September 2016–August 2017. Per cent calculations are row-wise.

Figure 2

Table 2 Mean ± SD total number of bats counted per day during the 12 survey days in the five caves at Gupteswar cave tourism and pilgrimage site (Fig. 1) during September 2016–August 2017.

Figure 3

Fig. 2 (a) Reproductive phenology (numbers of females pregnant and with pups) amongst the 140 bats captured, and (b) number of visitors at Gupteswar cave tourism and pilgrimage site (Fig. 1), during September 2016–August 2017.

Figure 4

Table 3 Number of tourists who visited the five caves at Gupteswar cave tourism and pilgrim site (Fig. 1) in each survey day during September 2016–August 2017. Values in parentheses are the number of tourist groups. The monthly totals are presented in Fig. 2b.

Figure 5

Table 4 Demographic characteristics of the local people (n = 76) and tourists (n = 366) interviewed to assess their knowledge and attitude towards bats at Gupteswar cave tourism and pilgrim site, eastern India, during September 2016–August 2017.

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