Ceballos, G. & Ehrlich, P. R. Mammal population losses and the extinction crisis. Science 296, 904–907 (2002).
Google Scholar
Morrison, J. C., Sechrest, W., Dinerstein, E., Wilcove, D. S. & Lamoreux, J. F. Persistence of large mammal faunas as indicators of global human impacts. J. Mammal. 88, 1363–1380 (2007).
Ripple, W. J. et al. Status and ecological effects of the world’s largest carnivores. Science 343, 1241484 (2014).
Google Scholar
Finnegan, S. P. et al. Reserve size, dispersal and population viability in wide ranging carnivores: the case of jaguars in Emas National Park, Brazil. Anim. Conserv. 24, 3–14 (2021).
Wang, T. et al. Amur tigers and leopards returning to China: direct evidence and a landscape conservation plan. Landsc. Ecol. 31, 491–503 (2016).
Gilbert, M. et al. Distemper, extinction, and vaccination of the Amur tiger. Proc. Natl. Acad. Sci. 117, 31954–31962 (2020).
Google Scholar
Smith, K. F., Acevedo-Whitehouse, K. & Pedersen, A. B. The role of infectious diseases in biological conservation. Anim. Conserv. 12, 1–12 (2009).
Wolf, C. & Ripple, W. J. Range contractions of the world’s large carnivores. R. Soc. Open Sci. 4, 170052 (2017).
Google Scholar
Courchamp, F. et al. Inverse density dependence and the Allee effect. Trends Ecol. Evol. 14, 405–410 (1999).
Google Scholar
Wittmann, M. J., Stuis, H. & Metzler, D. Genetic Allee effects and their interaction with ecological Allee effects. J. Anim. Ecol. 87, 11–23 (2018).
Google Scholar
Estes, J. A. et al. Trophic Downgrading of Planet Earth. Science 333, 301–306 (2011).
Google Scholar
Stein, A. B. et al. IUCN Red List of Threatened Species: Panthera pardus. IUCN Red List Threat. Species (2020).
Vitkalova, A. V. et al. Transboundary cooperation improves endangered species monitoring and conservation actions: A case study of the global population of Amur leopards. Conserv. Lett. 11, e12574 (2018).
Wang, T. et al. A science-based approach to guide Amur leopard recovery in China. Biol. Conserv. 210, 47–55 (2017).
Lewis, J. et al. Assessing the health risks of reintroduction: The example of the Amur leopard, Panthera pardus orientalis. Transbound. Emerg. Dis. 67, 1177–1188 (2020).
Google Scholar
Terio, K. A. & Craft, M. E. Canine distemper virus (CDV) in another big cat: should CDV be renamed carnivore distemper virus? mBio 4, e00702–e00713 (2013).
Google Scholar
Adhikari, R. B., Shrestha, M., Puri, G., Regmi, G. R. & Ghimire, T. R. Canine Distemper Virus (CDV): an emerging threat to Nepal’s wildlife. Appl. Sci. Technol. Ann. 1, 149–154 (2020).
Roelke-Parker, M. E. et al. A canine distemper virus epidemic in Serengeti lions (Panthera leo). Nature 379, 441–445 (1996).
Google Scholar
Mulia, B. H. et al. Exposure of Wild Sumatran Tiger (Panthera tigris sumatrae) to Canine Distemper Virus. J. Wildl. Dis. 57, 464–466 (2021).
Google Scholar
Gordon, C. H. et al. Canine distemper in endangered Ethiopian wolves. Emerg. Infect. Dis. 824–832 (2015) https://doi.org/10.3201/eid2105.141920.
Timm, S. F. et al. A suspected canine distemper epidemic as the cause of a catastrophic decline in Santa Catalina Island foxes (Urocyon littoralis catalinae). J. Wildl. Dis. 45, 333–343 (2009).
Google Scholar
Sulikhan, N. S. et al. Canine distemper virus in a wild Far Eastern leopard (Panthera pardus orientalis). J. Wildl. Dis. 54, 170–174 (2018).
Google Scholar
Gilbert, M. et al. Canine distemper virus as a threat to wild tigers in Russia and across their range. Integr. Zool. 10, 329–343 (2015).
Google Scholar
Almberg, E. S., Cross, P. C. & Smith, D. W. Persistence of canine distemper virus in the Greater Yellowstone Ecosystem’s carnivore community. Ecol. Appl. 20, 2058–2074 (2010).
Google Scholar
Cleaveland, S. et al. The conservation relevance of epidemiological research into carnivore viral diseases in the Serengeti. Conserv. Biol. 21, 612–622 (2007).
Google Scholar
Haydon, D. T. et al. Low-coverage vaccination strategies for the conservation of endangered species. Nature 443, 692–695 (2006).
Google Scholar
Hebblewhite, M., Miquelle, D. G., Murzin, A. A., Aramilev, V. V. & Pikunov, D. G. Predicting potential habitat and population size for reintroduction of the Far Eastern leopards in the Russian Far East. Biol. Conserv. 144, 2403–2413 (2011).
Jiang, G. et al. New hope for the survival of the Amur leopard in China. Sci. Rep. 5, 15475 (2015).
Google Scholar
Licht, D. S., Moen, R. A. & Romanski, M. Modeling viability of a potential Canada lynx reintroduction to Isle Royale national park. Nat. Areas J. 37, 170–177 (2017).
Menges, E. S. Population viability analysis for an endangered plant. Conserv. Biol. 4, 52–62 (1990).
Beissinger, S. R. & McCullough, D. R. Population viability analysis. J. Wildl. Manag. 67, 481–506 (2003).
Aresu, M. et al. Assessing the effects of different management scenarios on the conservation of small island vulture populations. Bird. Conserv. Int. 31, 111–128 (2021).
Benson, J. F. et al. Extinction vortex dynamics of top predators isolated by urbanization. Ecol. Appl. 29, e01868 (2019).
Google Scholar
Franklin, A. D., Lacy, R. C., Bauman, K. L., Traylor-Holzer, K. & Powell, D. M. Incorporating drivers of reproductive success improves population viability analysis. Anim. Conserv. 24, 386–400 (2021).
McCallum, H. Models for managing wildlife disease. Parasitology 143, 805–820 (2016).
Google Scholar
Bradshaw, C. J. A. et al. Novel coupling of individual-based epidemiological and demographic models predicts realistic dynamics of tuberculosis in alien buffalo. J. Appl. Ecol. 49, 268–277 (2012).
Shoemaker, K. T. et al. Effects of prey metapopulation structure on the viability of black-footed ferrets in plague-impacted landscapes: a metamodelling approach. J. Appl. Ecol. 51, 735–745 (2014).
Shaffer, M. L. Minimum population sizes for species conservation. BioScience 31, 131–134 (1981).
Seimon, T. A. et al. Canine distemper virus: an emerging disease in wild endangered Amur tigers (Panthera tigris altaica). mBio 4, e00410–e00413 (2013).
Google Scholar
Wang, T. et al. An introduction to Long-term Tiger-Leopard Observation Network based on camera traps in Northeast China. Biodivers. Sci. 28, 1059 (2020).
Gilbert, M. et al. Estimating the potential impact of canine distemper virus on the Amur tiger population (Panthera tigris altaica) in Russia. PLOS ONE 9, e110811 (2014).
Google Scholar
Fahrig, L. How much habitat is enough? Biol. Conserv. 100, 65–74 (2001).
Thatte, P., Joshi, A., Vaidyanathan, S., Landguth, E. & Ramakrishnan, U. Maintaining tiger connectivity and minimizing extinction into the next century: Insights from landscape genetics and spatially-explicit simulations. Biol. Conserv. 218, 181–191 (2018).
Hostetler, J. A., Onorato, D. P., Jansen, D. & Oli, M. K. A cat’s tale: the impact of genetic restoration on Florida panther population dynamics and persistence. J. Anim. Ecol. 82, 608–620 (2013).
Google Scholar
Johnson, W. E. et al. Genetic restoration of the Florida panther. Science 329, 1641–1645 (2010).
Google Scholar
Sankar, K. et al. Monitoring of reintroduced tigers in Sariska Tiger Reserve, Western India: preliminary findings on home range, prey selection and food habits. Trop. Conserv. Sci. 3, 301–318 (2010).
Kelly, P., Stack, D. & Harley, J. A review of the proposed reintroduction program for the Far Eastern leopard (Panthera pardus orientalis) and the role of conservation organizations, veterinarians, and zoos. Top. Companion Anim. Med. 28, 163–166 (2013).
Google Scholar
Hayward, M. W. & Somers, M. J. Reintroduction of top-order predators: using science to restore one of the drivers of biodiversity. in Reintroduction of Top-Order Predators 1–9 (John Wiley & Sons, Ltd, 2009). https://doi.org/10.1002/9781444312034.ch1.
Pujol, B., Zhou, S.-R., Sanchez Vilas, J. & Pannell, J. R. Reduced inbreeding depression after species range expansion. Proc. Natl Acad. Sci. 106, 15379–15383 (2009).
Google Scholar
He, C., Du, J., Zhu, D. & Zhang, L. Population viability analysis of small population: a case study for Asian elephant in China. Integr. Zool. 15, 350–362 (2020).
Google Scholar
Sugimoto, T., Aramilev, V. V., Nagata, J. & McCullough, D. R. Winter food habits of sympatric carnivores, Amur tigers and Far Eastern leopards, in the Russian Far East. Mamm. Biol. 81, 214–218 (2016).
Athreya, V., Odden, M., Linnell, J. D. C., Krishnaswamy, J. & Karanth, K. U. A cat among the dogs: leopard Panthera pardus diet in a human-dominated landscape in western Maharashtra, India. Oryx 50, 156–162 (2016).
Steinmetz, R., Seuaturien, N., Intanajitjuy, P., Inrueang, P. & Prempree, K. The effects of prey depletion on dietary niches of sympatric apex predators in Southeast Asia. Integr. Zool. 16, 19–32 (2021).
Google Scholar
Appel, M. J. G. et al. Canine distemper epizootic in lions, tigers, and leopards in North America. J. Vet. Diagn. Invest. 6, 277–288 (1994).
Google Scholar
Coltman, D. W., Pilkington, J. G., Smith, J. A. & Pemberton, J. M. Parasite-mediated selection against inbred Soay sheep in a free-living, island population. Evolution 53, 1259–1267 (1999).
Google Scholar
Fox, C. W. & Reed, D. H. Inbreeding depression increases with environmental stress: an experimental study and meta-analysis. Evolution 65, 246–258 (2011).
Google Scholar
Feng, L. et al. Collaboration brings hope for the last Amur leopards. Cat. N. 65, 20 (2017).
Lacy, R. C., Pollak, J. P., Miller, P. S., Hungerford, L. & Bright, P. Outbreak. Version 2.10. (2020).
Lacy, R. C. & Pollak, J. P. Vortex: A stochastic simulation of the extinction process. Version 10.4. (2021).
Pollak, J. P. & Lacy, R. C. Metamodel manager. Version 1.0.6. (2020).
Pacioni, C., Sullivan, S., Lees, C. M., Miller, P. S. & Lacy, R. C. Outbreak user’s manual. Version 1.1. (2020).
Roscoe, D. E. Epizootiology of canine-distemper in new-jersey raccoons. J. Wildl. Dis. 29, 390–395 (1993).
Google Scholar
Odden, M. & Wegge, P. Spacing and activity patterns of leopards Panthera pardus in the Royal Bardia National Park, Nepal. Wildl. Biol. 11, 145–152 (2005).
Stander, P. E., Haden, P. J., Kaqece, I. & Ghau, I. The ecology of asociality in Namibian leopards. J. Zool. 242, 343–364 (1997).
Huisman, J., Kruuk, L. E. B., Ellis, P. A., Clutton-Brock, T. & Pemberton, J. M. Inbreeding depression across the lifespan in a wild mammal population. Proc. Natl Acad. Sci. 113, 3585–3590 (2016).
Google Scholar
Morton, N. E., Crow, J. F. & Muller, H. J. An estimate of the mutational damage in man from data on consanguineous marriages. Proc. Natl Acad. Sci. 42, 855–863 (1956).
Google Scholar
Balme, G. A., Slotow, R. & Hunter, L. T. B. Edge effects and the impact of non-protected areas in carnivore conservation: leopards in the Phinda–Mkhuze Complex, South Africa. Anim. Conserv. 13, 315–323 (2010).
Kumbhojkar, S., Yosef, R., Mehta, A. & Rakholia, S. A camera-trap home-range analysis of the Indian leopard (Panthera pardus fusca) in Jaipur, India. Animals 10, 1600 (2020).
Google Scholar
Rozhnov, V. V. et al. Home range structure and space use of a female Amur leopard, Panthera pardus orientalis (Carnivora, Felidae). Biol. Bull. 42, 821–830 (2015).
Ralls, K., Ballou, J. D. & Templeton, A. Estimates of lethal equivalents and the cost of inbreeding in mammals. Conserv. Biol. 2, 185–193 (1988).
Hammersley, J. M. & Handscomb, D. C. General principles of the Monte Carlo method. in Monte Carlo Methods (eds. Hammersley, J. M. & Handscomb, D. C.) 50–75 (Springer Netherlands, 1964). https://doi.org/10.1007/978-94-009-5819-7_5.
Kenney, J. S., Allendorf, F. W., McDougal, C. & Smith, J. L. D. How much gene flow is needed to avoid inbreeding depression in wild tiger populations? Proc. R. Soc. B Biol. Sci. 281, 20133337 (2014).
O’Grady, J. J. et al. Realistic levels of inbreeding depression strongly affect extinction risk in wild populations. Biol. Conserv. 133, 42–51 (2006).
Miller, P. S., Lacy, R. C., Medina-Miranda, R., López-Ortiz, R. & Díaz-Soltero, H. Confronting the invasive species crisis with metamodel analysis: An explicit, two-species demographic assessment of an endangered bird and its brood parasite in Puerto Rico. Biol. Conserv. 196, 124–132 (2016).
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