Endangered anurans in a novel forest in the highlands of Sri Lanka
Rohan S. PethiyagodaA Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.
B Postgraduate Institute of Archaeology, University of Kelaniya, Colombo 7, Sri Lanka.
C Present address: University of Sydney Business School, Sydney, NSW 2006, Australia.
D Corresponding author. Email: sarith21@gmail.com
Wildlife Research 39(7) 641-648 https://doi.org/10.1071/WR12079
Submitted: 2 May 2012 Accepted: 20 August 2012 Published: 19 September 2012
Abstract
Context: Lands without agricultural or urban use embedded within agricultural and urban regions now account for ~35% of Earth’s terrestrial extent. Although created by human disturbances, these ‘novel ecosystems’, usually poor in native flora and often dominated by alien species, do not require human intervention for their maintenance. Given their large and increasing area, however, their ability to support native – and especially threatened – faunas warrants investigation. With 20 species already extinct and 47 of its 91 extant species assessed as Endangered or Critically Endangered, Sri Lanka’s amphibian fauna is in trouble. The 18 anurans (12 of these Endangered) occurring above 1500 m in the island’s central mountains are at particular risk from drastic declines in the extent and quality of habitat. Habitat restoration, however, is retarded by successional vegetation being arrested at least in the decadal time-frame by alien invasive species, creating a ‘novel ecosystem’.
Aim: To investigate whether such an ecosystem is able to support native anurans with a species richness and abundance comparable to that of neighbouring tropical montane cloud forest.
Methods: We surveyed 110 transects (each 20 m × 2 m) across three neighbouring locations covering three microhabitat-types, and recorded 552 specimens. One-way analyses of variance and post hoc, pair-wise Tukey’s tests were performed to test for differences in species richness and abundance among the three microhabitat types.
Key result: Of the 15 anuran species occurring in the neighbouring primary forest, 12 (eight of them Endangered) had established populations in the novel ecosystem (a former tea plantation), with abundances comparable to (or in some cases exceeding) those in primary forest.
Conclusion: Even young secondary forest dominated by alien plant species, in which native vegetation is almost wholly absent, can provide adequate habitat for most threatened highland anurans in Sri Lanka.
Implications: (1) Even if florally poor and dominated by alien species, novel ecosystems may present potential conservation opportunities for previously threatened faunas. (2) Threatened anurans exclusively dependent on primary forest and unable to utilise secondary-growth forest should receive greater conservation attention and be prioritised for in situ conservation measures. (3) Given their large and increasing extent globally, novel ecosystems should be considered as part of the area of occupancy of species able to complete their life cycles in them when assessed for conservation purposes, rather than being arbitrarily discarded as ‘degraded’.
Additional keywords: amphibian, Austroeupatorium, cloud forest, emerging ecosystem, novel ecosystem, secondary forest.
References
Bahir, M. M., Meegaskumbura, M., Manamendra-Arachchi, K., Schneider, C. J., and Pethiyagoda, R. (2005). Reproduction and terrestrial direct development in Sri Lankan shrub frogs (Amphibia: Ranidae: Rhacophorinae: Philautus). The Raffles Bulletin of Zoology 12, 339–350.Barlow, J., Gardner, T. A., Araujo, I. S., Ávila-Pires, T. C., Bonaldo, A. B., Costa, J. E., Esposito, M. C., Ferreira, L. V., Hawes, J., Hernandez, M. I. M., Hoogmoed, M. S., Leite, R. N., Lo-Man-Hung, N. F., Malcolm, J. R., Martins, M. B., Mestre, L. A. M., Miranda-Santos, R., Nunes-Gutjahr, A. L., Overal, W. L., Parry, L., Peters, S. L., Ribeiro-Junior, M. A., da Silva, M. N. F., da Silva Motta, C., and Peres, C. A. (2007). Quantifying the biodiversity value of tropical primary, secondary, and plantation forests. Proceedings of the National Academy of Sciences, USA 104, 18555–18560.
| Quantifying the biodiversity value of tropical primary, secondary, and plantation forests.Crossref | GoogleScholarGoogle Scholar |
Cincotta, R., Wisnewski, P. J., and Engelman, R. (2000). Human population in the biodiversity hotspots. Nature 404, 990–992.
| Human population in the biodiversity hotspots.Crossref | GoogleScholarGoogle Scholar |
Collins, J. P., and Crump, M. L. (2009). ‘Extinction in Our Times: Global Amphibian Decline.’ (Oxford University Press: Oxford, UK.)
Cook, W. M., Lane, K. T., Foster, B. L., and Holt, R. D. (2002). Island theory, matrix effects and species richness patterns in habitat fragments. Ecology Letters 5, 619–623.
| Island theory, matrix effects and species richness patterns in habitat fragments.Crossref | GoogleScholarGoogle Scholar |
Ewel, J. J., and Putz, F. E. (2004). A place for alien species in ecosystem restoration. Frontiers in Ecology and the Environment 2, 354–360.
| A place for alien species in ecosystem restoration.Crossref | GoogleScholarGoogle Scholar |
FPU (Forestry Planning Unit) (1995). Sri Lanka forestry sector master plan. Forestry Planning Unit, Ministry of Agriculture, Lands and Forestry, Battaramulla, Sri Lanka.
Gardner, T. A., Barlow, J., and Peres, C. A. (2007a). Paradox, presumption and pitfalls in conservation biology: the importance of habitat change for amphibians and reptiles. Biological Conservation 138, 166–179.
| Paradox, presumption and pitfalls in conservation biology: the importance of habitat change for amphibians and reptiles.Crossref | GoogleScholarGoogle Scholar |
Gardner, T. A., Ribeiro-Junior, M. A., Barlow, J., Ávila-Pires, T. C. S., Hoogmoed, M. S., and Peres, C. A. (2007b). The value of primary, secondary, and plantation forests for a Neotropical herpetofauna. Conservation Biology 21, 775–787.
| The value of primary, secondary, and plantation forests for a Neotropical herpetofauna.Crossref | GoogleScholarGoogle Scholar |
Gardner, T. A., Barlow, J., Chazdon, R., Ewers, R. M., Harvey, C. A., Peres, C. A., and Sodhi, N. S. (2009). Prospects for tropical forest biodiversity in a human-modified world. Ecology Letters 12, 561–582.
| Prospects for tropical forest biodiversity in a human-modified world.Crossref | GoogleScholarGoogle Scholar |
Gunatilleke, N., and Gunatilleke, S. (1995). Peak Wilderness and Horton Plains, Sri Lanka. In ‘Centres of Plant Diversity: a Guide and Strategy for their Conservation, vol. 2: Asia, Australasia and the Pacific’. (Eds S. D. Davis, V. H. Heywood and A. C. Hamilton.) pp. 127–131. (IUCN: Cambridge, UK.)
Hamilton, L. S., Juvik, J. O., and Scatena, F. N. (1994). The Puerto Rico Tropical Cloud Forest Symposium: Introduction and Workshop Synthesis. In ‘Tropical Montane Cloud Forests’. (Eds L. S. Hamilton, J. O. Juvik and F. N. Scatena.) pp. 1–23. (Springer Verlag: New York.)
Hobbs, R. J., Arico, S., Aronson, J., Baron, J. S., Bridgewater, P., Cramer, V. A., Epstein, P. R., Ewel, J. J., Klink, C. A., Lugo, A. E., Norton, D., Ojima, D., Richardson, D. M., Sanderson, E. W., Valladares, F., Vilà, M., Zamora, R., and Zobel, M. (2006). Novel ecosystems: theoretical and management aspects of the new ecological world order. Global Ecology and Biogeography 15, 1–7.
| Novel ecosystems: theoretical and management aspects of the new ecological world order.Crossref | GoogleScholarGoogle Scholar |
IUCN (The international Union for Conservation of Nature and Natural Resources) (2001). ‘IUCN Red List Categories and Criteria: Version 3.1.’ (IUCN Species Survival Commission, IUCN: Gland, Switzerland.)
IUCN (The international Union for Conservation of Nature and Natural Resources) (2012). ‘The IUCN Red List of Threatened Species.’ Available at http://www.iucnredlist.org/ [verified 10 October 2010].
Kudavidanage, E. P., Wanger, T. C., de Alwis, C., Sanjeewa, S., and Kotagama, S. W. (2012). Amphibian and butterfly diversity across a tropical land-use gradient in Sri Lanka; implications for conservation decision making. Animal Conservation 15, 253–265.
| Amphibian and butterfly diversity across a tropical land-use gradient in Sri Lanka; implications for conservation decision making.Crossref | GoogleScholarGoogle Scholar |
Lugo, A. E. (2009). The emerging era of novel tropical forests. Biotropica 41, 589–591.
| The emerging era of novel tropical forests.Crossref | GoogleScholarGoogle Scholar |
Lugo, A. E., and Helmer, E. (2004). Emerging forests on abandoned land: Puerto Rico’s new forests. Forest Ecology and Management 190, 145–161.
Manamendra-Arachchi, K., and Pethiyagoda, R. (2005). The Sri Lankan shrub frogs of the genus Philautus Gistel, 1848 (Ranidae: Rhacophorinae), with description of 27 new species. The Raffles Bulletin of Zoology 12, 163–303.
Manamendra-Arachchi, K., and Pethiyagoda, R. (2006). ‘Sri Lankan Amphibians.’ (WHT Publications: Colombo.) [In Sinhala]
Marris, E. (2009). Ragamuffin Earth. Nature 460, 450–453.
| Ragamuffin Earth.Crossref | GoogleScholarGoogle Scholar |
Marsh, D. M., and Haywood, L. M. B. (2010). Area-based surveys. In ‘Amphibian Ecology and Conservation’. (Ed. C. K. Dodd.) pp. 247–262. (Oxford University Press: Oxford, UK.)
Mascaro, J. K., Becklund, K., Hughes, R. F., and Schnitzer, S. A. (2008). Limited native plant regeneration in novel, exotic-dominated forests on Hawai’i. Forest Ecology and Management 256, 593–606.
| Limited native plant regeneration in novel, exotic-dominated forests on Hawai’i.Crossref | GoogleScholarGoogle Scholar |
Meegaskumbura, M., Manamendra-Arachchi, K., and Pethiyagoda, R. (2009). Two new species of shrub frogs (Rhacophoridae: Philautus) from the lowlands of Sri Lanka. Zootaxa 2122, 51–68.
Meegaskumbura, M., Manamendra-Arachchi, K., Bowatte, G., and Meegaskumbura, S. (2012). Rediscovery of Pseudophilautus semiruber, a diminutive shrub frog (Rhacophoridae: Pseudophilautus) from Sri Lanka. Zootaxa 3229, 58–68.
Melvani, K. (1997). Frog tea? Froglog 23, 2.
Perera, G. A. D. (2001). The secondary forest situation in Sri Lanka: a review. Journal of Tropical Forest Science 13, 768–785.
Pethiyagoda, R. S., and Nanayakkara, S. (2011). Invasion by Austroeupatorium inulifolium (Asteraceae) arrests succession following tea cultivation in the highlands of Sri Lanka. Ceylon Journal of Science 40, 175–181.
Ramanamanjato, J.-B., McIntyre, P. B., and Nussbaum, R. A. (2002). Reptile, amphibian, and lemur diversity of the Malahelo Forest, a biogeographical transition zone in southeastern Madagascar. Biodiversity and Conservation 11, 1791–1807.
| Reptile, amphibian, and lemur diversity of the Malahelo Forest, a biogeographical transition zone in southeastern Madagascar.Crossref | GoogleScholarGoogle Scholar |
Senaratne, P. M. (2005). ‘Forests of Sri Lanka.’ (Sarasavi: Colombo.)
Stuart, S. N., Hoffman, M., Chanson, J. S., Cox, N. A., and others (2008). ‘Threatened Amphibians of the World.’ (Lynx Edicions: Barcelona.)
Vallan, D. (2002). Effects of anthropogenic environmental changes on amphibian diversity in the rain forests of eastern Madagascar. Journal of Tropical Ecology 18, 725–742.
| Effects of anthropogenic environmental changes on amphibian diversity in the rain forests of eastern Madagascar.Crossref | GoogleScholarGoogle Scholar |
Werner, W. (2001). ‘Sri Lanka’s Magnificent Cloud Forests.’ (WHT Publications: Colombo.)
Wijesinghe, M. R., and Brooke, M. de L. (2005). Impact of habitat disturbance on the distribution of endemic species of small mammals and birds in a tropical rain forest in Sri Lanka. Journal of Tropical Ecology 21, 661–668.
| Impact of habitat disturbance on the distribution of endemic species of small mammals and birds in a tropical rain forest in Sri Lanka.Crossref | GoogleScholarGoogle Scholar |
Wikramanayake, E. D., and Gunatilleke, S. (2002). Sri Lanka’s montane rain forests. In ‘Terrestrial Ecoregions of the Indo-Pacific: a Conservation Assessment’. (Eds E. D. Wikramanayake, E. Dinerstein, C. Loucks, D. Olson, J. Morrison, J. Lamoreux, M. McKnight and P. Hedao.) pp. 290–293. (Island Press: Washington, DC.)