International Journal of Primatology

, Volume 33, Issue 2, pp 305–321 | Cite as

Spatial Ecology of the Endangered Milne-Edwards’ Sifaka (Propithecus edwardsi): Do Logging and Season Affect Home Range and Daily Ranging Patterns?

  • Brian D. Gerber
  • Summer Arrigo-Nelson
  • Sarah M. Karpanty
  • Mary Kotschwar
  • Patricia C. Wright
Article

Abstract

Primates often live in human-altered habitats; Malagasy lemurs are no exception. It is important to understand if habitat alteration affects primates’ space use patterns across multiple spatial and temporal scales, as this drives population density. We quantified the daily, seasonal, and annual space-use of seven groups of Milne-Edwards’ sifaka (Propithecus edwardsi) living in unlogged and logged rain forest in Ranomafana National Park, Madagascar between December 2002 and November 2003. Concurrent data showed that sifakas consumed higher quality foods in the unlogged than in logged forests; thus we explored how space use patterns were related to energy use strategies. Sifaka groups in the logged rain forest traveled 7–13% less per day than groups in the unlogged rain forest, despite their larger home ranges (median: 46.12 and 23.52 ha, in the logged and unlogged forests, respectively). Sifakas may thus use an energy-minimizing strategy at the scale of the individual day but an energy-maximizing strategy at the annual home range scale. Sifakas exhibited fidelity to the home range across seasons, but their core area of use shifted considerably with season. We found no difference in population density between sites. However, given the interannual variability in sifaka foods, a multiyear study is needed to assess if energy strategies observed in this study are consistent across longer time periods. Our findings suggest that lemurs may persist in logged habitats by altering spatial use patterns; future work should attempt to quantify the threshold level of forest regeneration from logging that will allow lemurs to persist at similar densities as in unlogged forest.

Keywords

Daily path length Home range Lemur Logging Rain forest 

References

  1. Altmann, J. (1974). Observational study of behavior: sampling behavior. Behaviour, 49, 227–267.PubMedCrossRefGoogle Scholar
  2. Arrigo-Nelson, S. (2006). The impact of habitat disturbance on the feeding ecology of the Milne-Edwards’ sifaka (Propithecus edwardsi) in Ranomafana National Park, Madagascar. Ph.D. dissertation, State University of New York, Stony Brook.Google Scholar
  3. Arrigo-Nelson, S. J., & Randriamahaleo, S. I. (2006). The impact of habitat disturbance on sifaka resource distribution and abundance within Ranomafana National Park, Madagascar. International Journal of Primatology, 27(S1), 498.Google Scholar
  4. Balko, E. A., & Underwood, H. B. (2005). Effects of forest structure and composition on food availability for Varecia variegata at Ranomafana National Park, Madagascar. American Journal of Primatology, 66, 45–70.PubMedCrossRefGoogle Scholar
  5. Bannar-Martin, K. H. (2009). Interior versus exterior forest edges: Their effect on the home range, spatial ecology and feeding ecology of Milne-Edwards’ sifakas (Propithecus edwardsi) in Ranomafana National Park, Madagascar. M.S. thesis, University of Toronto, Toronto.Google Scholar
  6. Blundell, G. M., Maier, J. A. K., & Debevec, E. M. (2001). Linear home ranges: effects of smoothing, sample size, and autocorrelation on kernel estimates. Ecological Monographs, 71, 469–489.CrossRefGoogle Scholar
  7. Brown, K. A., & Gurevitch, J. (2004). Long-term impacts of logging on forest diversity in Madagascar. Proceedings of the National Academy of Sciences of the USA, 101, 6045–6049.PubMedCrossRefGoogle Scholar
  8. Burnham, K. P., & Anderson, D. R. (2002). Model selection and multimodel inference: A practical information-theoretic approach. New York: Springer-Verlag.Google Scholar
  9. Cade, B. S., & Richards, J. D. (2005). User manual for Blossom statistical software: U.S. Geological Survey Open-File Report 2005–1353. 1–124.Google Scholar
  10. Calenge, C. (2006). The package “adehabitat” for the R software: a tool for the analysis of space and habitat use by animals. Ecological Modelling, 197, 516–519.CrossRefGoogle Scholar
  11. Chapman, C. A., Balcomb, S. R., Gillespie, T. R., Skorupa, J. P., & Struhsaker, T. T. (2000). Long-term effects of logging on African primate communities: a 28-year comparison from Kibale National Park, Uganda. Conservation Biology, 14, 207–217.CrossRefGoogle Scholar
  12. Clutton-Brock, T. H. (1977). Some aspects of intra-specific variation in feeding and ranging behaviour in primates. In T. H. Clutton-Brock (Ed.), Primate ecology (pp. 539–556). New York: Academic Press.Google Scholar
  13. Clutton-Brock, T. H., & Harvey, P. H. (1977). Primate ecology and social organization. Journal of Zoology, 183, 1–39.CrossRefGoogle Scholar
  14. Conservation International. (2011). Center for Applied Biodiversity Science. Retrieved from https://learning.conservation.org/spatial_monitoring/Forest/Pages/default.aspx. Accessed July 27, 2011.
  15. Cowlishaw, G., Pettifor, R. A., & Isaac, N. J. B. (2009). High variability in patterns of population decline: the importance of local processes in species extinctions. Proceedings of the Royal Society B: Biological Sciences, 276, 63–69.PubMedCrossRefGoogle Scholar
  16. De Solla, S. R., Bonduriansky, R., & Brooks, R. J. (1999). Eliminating autocorrelation reduces biological relevance of home range estimates. Journal of Animal Ecology, 68, 221–234.CrossRefGoogle Scholar
  17. Dewar, R. E., & Richard, A. F. (2007). Evolution in the hypervariable environment of Madagascar. Proceedings of the National Academy of Sciences of the USA, 104, 13723–13727.PubMedCrossRefGoogle Scholar
  18. Dunham, A. E., Erhart, E. M., Overdorff, D. J., & Wright, P. C. (2008). Evaluating effects of deforestation, hunting, and El Niño events on a threatened lemur. Biological Conservation, 141, 287–297.CrossRefGoogle Scholar
  19. Erhart, E. M., & Overdorff, D. J. (2008). Spatial memory during foraging in prosimian primates: Propithecus edwardsi and Eulemur fulvus rufus. Folia Primatologica, 79, 185–196.CrossRefGoogle Scholar
  20. Fan, P.-F., Ni, Q.-Y., Sun, G.-Z., Huang, B., & Jiang, X.-L. (2008). Seasonal variations in the activity budget of Nomascus concolor jingdongensis at Mt. Wuliang, Central Yunnan, China: effects of diet and temperature. International Journal of Primatology, 29, 1047–1057.CrossRefGoogle Scholar
  21. Fieberg, J. (2007). Kernel density estimators of home range: smoothing and the autocorrelation red herring. Ecology, 88, 1059–1066.PubMedCrossRefGoogle Scholar
  22. Fieberg, J., & Kochanny, C. O. (2005). Quantifying home-range overlap: the importance of the ultization distribution. Journal of Wildlife Management, 69, 1346–1359.CrossRefGoogle Scholar
  23. Foltz, J. (2009). Structure d’une communauté de propithèques de Milne-Edwards (Propithecus edwardsi) dans une forêt fragmentée malgache : Approches démographique, génétique et comportementale. Ph.D. dissertation, Universite de Strasbourg, Strasbourg, France.Google Scholar
  24. Ganas, J., & Robbins, M. M. (2005). Ranging behavior of the mountain gorillas (Gorilla beringei beringei) in Bwindi Impenetrable National Park, Uganda: a test of the ecological constraints model. Behavioral Ecology and Sociobiology, 58, 277–288.CrossRefGoogle Scholar
  25. Glander, K. E., Wright, P. C., Daniels, P. S., & Merenlender, A. M. (1992). Morphometrics and testicle size of rain forest lemur species from southeastern Madagascar. Journal of Human Evolution, 22, 1–17.CrossRefGoogle Scholar
  26. Graham, M. H. (2003). Confronting multicollinearity in ecological multiple regression. Ecology, 84, 2809–2815.CrossRefGoogle Scholar
  27. Grant, J. W. A., Chapman, C. A., & Richardson, K. S. (1992). Defended versus undefended home range size of carnivores, ungulates and primates. Behavioral Ecology and Sociobiology, 31, 149–161.CrossRefGoogle Scholar
  28. Hemingway, C. A. (1998). Selectivity and variability in the diet of Milne-Edwards’ sifakas (Propithecus diadema edwardsi): implications for folivory and seed-eating. International Journal of Primatology, 19, 355–377.CrossRefGoogle Scholar
  29. Hemingway, C. A., & Bynum, N. (2005). The influence of seasonality on primate diet and ranging seasonality in primates. In D. K. Brockman & Schaik CPv (Eds.), Seasonality in primates studies of living and extinct human and non-human primates. Cambridge, UK: Cambridge University Press.Google Scholar
  30. Horne, J. S., & Garton, E. O. (2006). Selecting the best home range model: an information theoretic approach. Ecology, 87, 1146–1152.PubMedCrossRefGoogle Scholar
  31. Irwin, M. T. (2008). Diademed sifaka (Propithecus diadema) ranging and habitat use in continuous and fragmented forest: higher density but lower viability in fragments? Biotropica, 40, 231–240.CrossRefGoogle Scholar
  32. Isbell, L. A. (2004). Is there no place like home? Ecolgical bases of dispersal in primates and their consequences for the formation of kin groups. In B. Chapais & C. Berman (Eds.), Kinship and behavior in primates (pp. 71–108). New York: Oxford University Press.Google Scholar
  33. IUCN. (2011). IUCN Red List of Threatened Species v. 2011.1. Retrieved from http://www.iucnredlist.org. Accessed October 6, 2011.
  34. Jetz, W., Carbone, C., Fulford, J., & Brown, J. H. (2004). The scaling of animal space use. Science, 306, 266–268.PubMedCrossRefGoogle Scholar
  35. Johns, A., & Skorupa, J. (1987). Responses of rain-forest primates to habitat disturbance: a review. International Journal of Primatology, 8, 157–191.CrossRefGoogle Scholar
  36. Johnson, D. H. (1980). The comparison of usage and availability measurements for evaluating resource preference. Ecology, 61, 65–71.CrossRefGoogle Scholar
  37. Kernohan, B. J., Gitzen, R. A., & Millspaugh, J. J. (2001). Analysis of animal space use and movements. In J. J. Milspaugh & J. M. Marzluff (Eds.), Radio tracking and animal populations (pp. 125–166). New York: Academic Press.CrossRefGoogle Scholar
  38. Koenig, A., Beise, J., Chalise, M. K., & Ganzhorn, J. U. (1998). When females should contest for food—testing hypotheses about resource density, distribution, size, and quality with hanuman langurs (Presbytis entellus). Behavioral Ecology and Sociobiology, 42, 225–237.CrossRefGoogle Scholar
  39. Kotschwar, M. (2010). Variation in predator communities and anti-predator behaviors of lemurs in southeastern Madagascar. M.S. thesis, Virginia Tech, Blacksburg.Google Scholar
  40. Laver, P. (2005). Abode: Kernel home range estimation for ArcGIS using VBA and ArcObjects. Retrieved from http://fishwild.vt.edu/abode/abodeweb.html. Accessed October 6, 2011.
  41. Lewis, R. J., & Kappeler, P. M. (2005). Seasonality, body condition, and timing of reproduction in Propithecus verreauxi verreauxi in the Kirindy Forest. American Journal of Primatology, 67, 347–364.PubMedCrossRefGoogle Scholar
  42. Li, Z., & Rogers, M. E. (2005). Habitat quality and range use of white-headed langurs in Fusui, China. Folia Primatologica, 76, 185–195.CrossRefGoogle Scholar
  43. Li, B., Chen, C., Ji, W., & Ren, B. (2000). Seasonal home range changes of the Sichuan snub-nosed monkey (Rhinopithecus roxellana) in the Qinling Mountains of China. Folia Primatologica, 71, 375–386.CrossRefGoogle Scholar
  44. Meyers, D. M., & Wright, P. C. (1993). Resource tracking: Food availability and Propithecus seasonal reproduction. In P. N. Kappeler & J. U. Ganzhorn (Eds.), Lemur social systems and their ecological basis (pp. 179–192). New York: Plenum Press.Google Scholar
  45. Mielke, P. W., Jr., & Berry, K. J. (2001). Permutation methods: A distance function approach. New York: Springer-Verlag.Google Scholar
  46. Milton, K., & May, M. L. (1976). Body weight, diet and home range area in primates. Nature, 259, 459–462.PubMedCrossRefGoogle Scholar
  47. Mitani, J. C., & Rodman, P. S. (1979). Territoriality: the relation of ranging pattern and home range size to defendability, with an analysis of territoriality among primate species. Behavioral Ecology and Sociobiology, 5, 241–251.CrossRefGoogle Scholar
  48. Moorcroft, P. R., & Lewis, M. A. (2006). Mechanistic home range analysis. Princeton, NJ: Princeton University Press.Google Scholar
  49. Morales, J. M., Moorcroft, P. R., Matthiopoulos, J., Frair, J. L., Kie, J. G., Powell, R. A., et al. (2010). Building the bridge between animal movement and population dynamics. Philosophical Transactions of the Royal Society B: Biological Sciences, 365, 2289–2301.CrossRefGoogle Scholar
  50. Morelli, T. L., King, S. J., Pochron, S. T., & Wright, P. C. (2009). The rules of disengagement: takeovers, infanticide, and dispersal in a rainforest lemur, Propithecus edwardsi. Behaviour, 146, 499–523.CrossRefGoogle Scholar
  51. Nams, V. O. (2005). Using animal movement paths to measure response to spatial scale. Oecologia, 143, 179–188.PubMedCrossRefGoogle Scholar
  52. Norscia, I., Carrai, V., & Borgognini-Tarli, S. M. (2006). Influence of dry season and food quality and quantity on behavior and deeding strategy of Propithecus verreauxi in Kirindy, Madagascar. International Journal of Primatology, 27, 1001–1022.CrossRefGoogle Scholar
  53. Ostro, L. E. T., Silver, S. C., Koontz, F. W., Young, T. P., & Horwich, R. H. (1999). Ranging behavior of translocated and established groups of black howler monkeys Alouatta pigra in Belize, Central America. Biological Conservation, 87, 181–190.CrossRefGoogle Scholar
  54. Otis, D. L., & White, G. C. (1999). Autocorrelation of location estimates and the analysis of radiotracking data. Journal of Wildlife Management, 63, 1039–1044.CrossRefGoogle Scholar
  55. Pochron, S. T., Morelli, T. L., Scirbona, J., & Wright, P. C. (2005). Sex differences in scent marking in Propithecus edwardsi of Ranomafana National Park, Madagascar. American Journal of Primatology, 66, 97–110.PubMedCrossRefGoogle Scholar
  56. Pochron, S. T., Tucker, W. T., & Wright, P. C. (2004). Demography, life history, and social structure in Propithecus diadema edwardsi from 1986–2000 in Ranomafana National Park, Madagascar. American Journal of Physical Anthropology, 125, 61–72.PubMedCrossRefGoogle Scholar
  57. Powzyk, J. A. (1997). The socio-ecology of two sympatric indriids: Propithecus diadema diadema and Indri indri, a comparison of feeding strategies and their possible repercussions on species-specific behaviors. Ph.D. disseretation, Duke University, Durham.Google Scholar
  58. R Development Core Team. (2010). R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing.Google Scholar
  59. Rodgers, A. R., Carr, A. P., Beyer, H. L., Smith, L., & Kie, J. G. (2007). HRT: Home range tools for ArcGIS. Thunder Bay, Ontario: Ontario Ministry of Natural Resources, Centre for Northern Forest Ecosystem Research.Google Scholar
  60. Senft, R. L., Coughenour, M. B., Bailey, D. W., Rittenhouse, L. R., Sala, O. E., & Swift, D. M. (1987). Large herbivore foraging and ecological hierarchies. Bioscience, 37(11), 789–799.CrossRefGoogle Scholar
  61. Silverman, B. W. (1986). Density estimation for statistics and data analysis. London: Chapman and Hall.Google Scholar
  62. Steenbeek, R., & Schaik, C. Pv. (2001). Competition and group size in Thomas’s langurs (Presbytis thomasi): the folivore paradox revisited. Behavioral Ecology and Sociobiology, 49, 100–110.CrossRefGoogle Scholar
  63. Steury, T. D., McCarthy, J. E., Roth, T. C., Lima, S. L., & Murray, D. L. (2010). Evaluation of root-n bandwidth selectors for kernel density estimation. Journal of Wildlife Management, 74(3), 539–548.CrossRefGoogle Scholar
  64. Strier, K. B. (1992). Atelinae adaptations: behavioral strategies and ecological constraints. American Journal of Physical Anthropology, 88, 515–524.PubMedCrossRefGoogle Scholar
  65. Takasaki, H. (1981). Troop size, habitat quality, and home range area in Japanese macaques. Behavioral Ecology and Sociobiology, 9(4), 277–281.CrossRefGoogle Scholar
  66. van Schaik, C., & van Hooff, J. (1983). On the ultimate causes of primate social systems. Behaviour, 85, 91–117.CrossRefGoogle Scholar
  67. van Schaik, C. P., & van Noordwijk, M. A. (1985). Interannual variability in fruit abundance and the reproductive seasonality in Sumatran long-tailed macaques (Macaca fascicularis). Journal of Zoology, 206, 533–549.CrossRefGoogle Scholar
  68. Wieczkowski, J. (2005). Examination of increased annual range of a Tana mangabey (Cercocebus galeritus) group. American Journal of Physical Anthropology, 128, 381–388.PubMedCrossRefGoogle Scholar
  69. Wilson, R. R., Hooten, M. B., Strobel, B. N., & Shivik, J. A. (2010). Accounting for individuals, uncertainty, and multiscale clustering in core area estimation. Journal of Wildlife Management, 74, 1343–1352.Google Scholar
  70. Wright, P. (1995). Demography and life history of free-ranging Propithecus diadema edwardsi in Ranomafana National Park, Madagascar. International Journal of Primatology, 16, 835–854.CrossRefGoogle Scholar
  71. Wright, P. C. (1997). The future of biodiversity in Madagascar. In S. M. Goodman & B. D. Patterson (Eds.), Natural change and human impact in Madagascar (pp. 381–405). Washington, DC: Smithsonian Institution Scholarly Press.Google Scholar
  72. Wright, P. C. (1999). Lemur traits and Madagascar ecology: coping with an island environment. Yearbook of Physical Anthropology, 42, 31–72.CrossRefGoogle Scholar
  73. Wright, P. C., & Andriamihaja, B. A. (2003). The conservation value of long-term research: a case study from Parc National de Ranomafana. In S. Goodman & J. Benstead (Eds.), Natural history of Madagascar. Chicago: University of Chicago Press.Google Scholar
  74. Wright, P. C., Razafindratsita, V. R., Pochron, S. T., & Jernvall, J. (2005). The key to Madagascar frugivores. In J. L. Dew & J. P. Boubli (Eds.), Tropical fruits and frugivores (pp. 121–138). Dordrecht: Springer.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  • Brian D. Gerber
    • 1
    • 2
  • Summer Arrigo-Nelson
    • 3
  • Sarah M. Karpanty
    • 1
  • Mary Kotschwar
    • 1
  • Patricia C. Wright
    • 4
  1. 1.Department of Fish and Wildlife ConservationVirginia TechBlacksburgUSA
  2. 2.Colorado State UniversityFort CollinsUSA
  3. 3.Department of Biological & Environmental SciencesCalifornia University of PennsylvaniaCaliforniaUSA
  4. 4.Department of AnthropologyStony Brook UniversityStony BrookUSA

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