Hostname: page-component-cd9895bd7-dk4vv Total loading time: 0 Render date: 2024-12-27T06:52:33.777Z Has data issue: false hasContentIssue false

Habitat use, activity patterns and use of mineral licks by five species of ungulate in south-eastern Peru

Published online by Cambridge University Press:  01 May 2009

Mathias W. Tobler*
Affiliation:
Botanical Research Institute of Texas, Andes to Amazon Biodiversity Program, 500 E 4th Street, Fort Worth, TX 76102, and Texas A&M University, Department of Wildlife and Fisheries Sciences, College Station, TX, USA
Samia E. Carrillo-Percastegui
Affiliation:
World Wildlife Fund U.S., 1250 24th Street NW, Washington, DC 20037, USA
George Powell
Affiliation:
World Wildlife Fund U.S., 1250 24th Street NW, Washington, DC 20037, USA
*
1Corresponding author. Email: matobler@brit.org

Abstract:

We studied the habitat use, activity patterns and use of mineral licks by five species of Amazonian ungulate using data from four 60-d camera trap surveys at two different sites in the lowland rain forest of Madre de Dios, Peru. Camera traps were set out in two regular grids with 40 and 43 camera stations covering an area of 50 and 65 km2, as well as at five mineral licks. Using occupancy analysis we tested the hypothesis that species are spatially separated. The results showed that the grey brocket deer (Mazama gouazoubira) occurred almost exclusively in terra firme forests, and that the white-lipped peccary (Tayassu pecari) used floodplain forest more frequently during some surveys. All other species showed no habitat preference and we did not find any spatial avoidance of species. The white-lipped peccary, the collared peccary (Pecari tajacu) as well as the grey brocket deer were strictly diurnal while the lowland tapir (Tapirus terrestris) was nocturnal. The red brocket deer (Mazama americana) was active day and night. The tapir was the species with the highest number of visits to mineral licks (average 52.8 visits per 100 d) followed by the white-lipped peccary (average 16.1 visits per 100 d) and the red brocket deer (average 17.1 visits per 100 d). The collared peccary was only recorded on three occasions and the grey brocket deer was never seen at a lick. Our results suggest that resource partitioning takes place mainly at the diet level and less at a spatial level; however, differences in small-scale habitat use are still possible.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

LITERATURE CITED

ALVARD, M. S., ROBINSON, J. G., REDFORD, K. H. & KAPLAN, H. 1997. The sustainability of subsistence hunting in the Neotropics. Conservation Biology 11:977982.CrossRefGoogle Scholar
AYALA, G. M. C. 2003. Monitoreo de Tapirus terrestris en el Izozog (Cerro Cortado) mediante el uso de telemetria como base para un plan de conservación. MSc thesis. Universidad Mayor de San Andres, Santa Cruz, Bolivia. 100 pp.Google Scholar
BECK, H. 2005. Seed predation and dispersal by peccaries throughout the Neotropics and its consequences: a review and synthesis. Pp. 77115 in Forget, P.-M., Lambert, J. E., Hulme, P. E. & Vander Wall, S. B. (eds.). Seed fate: predation, dispersal and seedling establishment. CABI Publishing, Wallingford.CrossRefGoogle Scholar
BODMER, R. E. 1990. Responses of ungulates to seasonal inundations in the Amazon floodplain. Journal of Tropical Ecology 6:191201.CrossRefGoogle Scholar
BODMER, R. E. 1991. Influence of digestive morphology on resource partitioning in Amazonian ungulates. Oecologia 85:361365.CrossRefGoogle ScholarPubMed
BODMER, R. E. 1995. Managing Amazonian wildlife – biological correlates of game choice by detribalized hunters. Ecological Applications 5:872877.CrossRefGoogle Scholar
BRANAN, W. V., WERKHOVEN, M. C. M. & MARCHINTON, R. L. 1985. Food-habits of brocket and white-tailed deer in Suriname. Journal of Wildlife Management 49:972976.CrossRefGoogle Scholar
BURNHAM, K. P. & ANDERSON, D. R. 1998. Model selection and inference: a practical information-theoretic approach. Springer, New York. 353 pp.CrossRefGoogle Scholar
CARRILLO, E., SAENZ, J. C. & FULLER, T. K. 2002. Movements and activities of white-lipped peccaries in Corcovado National Park, Costa Rica. Biological Conservation 108:317324.CrossRefGoogle Scholar
COELHO, I. P. 2006. Relações entre barreiros e a fauna de vertebrados no Pantanal, Brasil. M.Sc. thesis, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil. 56 pp.Google Scholar
DORAZIO, R. M. 2007. On the choice of statistical models for estimating occurrence and extinction from animal surveys. Ecology 88:27732782.CrossRefGoogle ScholarPubMed
DUARTE, J. M. B., GONZALEZ, S. & MALDONADO, J. E. 2008. The surprising evolutionary history of South American deer. Molecular Phylogenetics and Evolution 49:1722.CrossRefGoogle ScholarPubMed
EMMONS, L. & FEER, F. 1997. Neotropical rainforest mammals: a field guide. (Second edition). University of Chicago Press, Chicago. 307 pp.Google Scholar
EMMONS, L. H. & STARK, N. M. 1979. Elemental composition of a natural mineral lick in Amazonia. Biotropica 11:311313.CrossRefGoogle Scholar
FRAGOSO, J. M. V. 1998. Home range and movement patterns of white-lipped peccary (Tayassu pecari) herds in the northern Brazilian Amazon. Biotropica 30:458469.CrossRefGoogle Scholar
FRAGOSO, J. M. V. 1999. Perception of scale and resource partitioning by peccaries: behavioral causes and ecological implications. Journal of Mammalogy 80:9931003.Google Scholar
FRAGOSO, J. M. V. & HUFFMAN, J. M. 2000. Seed-dispersal and seedling recruitment patterns by the last Neotropical megafaunal element in Amazonia, the tapir. Journal of Tropical Ecology 16:369385.CrossRefGoogle Scholar
GAYOT, M., HENRY, O., DUBOST, G. & SABATIER, D. 2004. Comparative diet of the two forest cervids of the genus Mazama in French Guiana. Journal of Tropical Ecology 20:3143.CrossRefGoogle Scholar
GIBBS, J. P. 2000. Monitoring populations. Pp. 213252 in Boitani, L. & Fuller, T. K. (eds.). Research techniques in animal ecology: controversies and consequences. Columbia University Press, New York.Google Scholar
GÓMEZ, H., WALLACE, R. B., AYALA, G. & TEJADA, R. 2005. Dry season activity periods of some Amazonian mammals. Studies on Neotropical Fauna and Environment 40:9195.CrossRefGoogle Scholar
HARDIN, G. 1960. The competitive exclusion principle. Science 131:12921297.CrossRefGoogle ScholarPubMed
HENRY, O., FEER, F. & SABATIER, D. 2000. Diet of the lowland tapir (Tapirus terrestris L.) in French Guiana. Biotropica 32:364368.CrossRefGoogle Scholar
HOLDO, R. M., DUDLEY, J. P. & MCDOWELL, L. R. 2002. Geophagy in the African elephant in relation to availability of dietary sodium. Journal of Mammalogy 83:652664.2.0.CO;2>CrossRefGoogle Scholar
HURTADO-GONZALES, J. L. & BODMER, R. E. 2004. Assessing the sustainability of brocket deer hunting in the Tamshiyacu-Tahuayo Communal Reserve, northeastern Peru. Biological Conservation 116:17.CrossRefGoogle Scholar
JONES, R. L. & HANSON, H. C. 1985. Mineral licks, geophagy, and biogeochemistry of North American ungulates. Iowa State University Press, Ames. 301 pp.Google Scholar
JUDAS, J. & HENRY, O. 1999. Seasonal variation of home range of collared peccary in tropical rain forests of French Guiana. Journal of Wildlife Management 63:546552.CrossRefGoogle Scholar
KARANTH, K. U. & NICHOLS, J. D. 1998. Estimation of tiger densities in India using photographic captures and recaptures. Ecology 79:28522862.CrossRefGoogle Scholar
KEUROGHLIAN, A., EATON, D. P. & LONGLAND, W. S. 2004. Area use by white-lipped and collared peccaries (Tayassu pecari and Tayassu tajacu) in a tropical forest fragment. Biological Conservation 120:411425.CrossRefGoogle Scholar
KILTIE, R. A. 1982. Bite force as a basis for niche differentiation between rain-forest peccaries (Tayassu tajacu and Tayassu pecari). Biotropica 14:188195.CrossRefGoogle Scholar
KILTIE, R. A. & TERBORGH, J. 1983. Observations on the behavior of rain-forest peccaries in Peru – why do white-lipped peccaries form herds. Zeitschrift für Tierpsychologie 62:241255.CrossRefGoogle Scholar
KLAUS, G. 1998. Natural licks and geophagy (soil ingestion) by large mammal species in the rain forest of the Central African Republic. Ph.D. thesis. University of Zürich, Zürich, Switzerland.Google Scholar
KREULEN, D. A. 1985. Lick use by large herbivores – a review of benefits and banes of soil consumption. Mammal Review 15:107123.CrossRefGoogle Scholar
MACKENZIE, D. I. & NICHOLS, J. D. 2004. Occupancy as a surrogate for abundance estimation. Animal Biodiversity and Conservation 27:461467.Google Scholar
MACKENZIE, D. I., NICHOLS, J. D., LACHMAN, G. B., DROEGE, S., ROYLE, J. A. & LANGTIMM, C. A. 2002. Estimating site occupancy rates when detection probabilities are less than one. Ecology 83:22482255.CrossRefGoogle Scholar
MACKENZIE, D. I., BAILEY, L. L. & NICHOLS, J. D. 2004. Investigating species co-occurrence patterns when species are detected imperfectly. Journal of Animal Ecology 73:546555.CrossRefGoogle Scholar
MACKENZIE, D. I., NICHOLS, J. D., ROYLE, J. A., POLLOCK, K. H., BAILEY, L. L. & HINES, J. E. 2006. Occupancy estimation and modeling: inferring patterns and dynamics of species occurrence. Elsevier, Amsterdam. 324 pp.Google Scholar
MAFFEI, L. & TABER, A. B. 2003. Area de acción de Mazama americana (Cervidae) en un bosque seco de Bolivia. Ecología en Bolivia 38:179180.Google Scholar
MAFFEI, L., CUÉLLAR, E. & NOSS, A. J. 2002. Uso de trampas-cámara para la evaluacón de mamíferos en el ecotono Chaco-Chiquitanía. Revista Boliviana de Ecología y Conservación 11:5565.Google Scholar
MILLS, A. & MILEWSKI, A. 2007. Geophagy and nutrient supplementation in the Ngorongoro Conservation Area, Tanzania, with particular reference to selenium, cobalt and molybdenum. Journal of Zoology 271:110118.CrossRefGoogle Scholar
MOE, S. R. 1993. Mineral-content and wildlife use of soil licks in southwestern Nepal. Canadian Journal of Zoology 71:933936.CrossRefGoogle Scholar
MONTENEGRO, O. L. 1998. The behavior of Lowland Tapir (Tapirus terrestris) at a natural mineral lick in the Peruvian Amazon. M.Sc. thesis. University of Florida, Gainsville, Florida, USA.Google Scholar
MONTENEGRO, O. L. 2004. Natural licks as keystone resources for wildlife and people in Amazonia. Ph.D. thesis. University of Florida, Gainsville, Florida, USA.Google Scholar
PERES, C. A. 1996. Population status of white-lipped Tayassu pecari and collared peccaries T. tajacu in hunted and unhunted Amazonian forests. Biological Conservation 77:115123.CrossRefGoogle Scholar
PERES, C. A. 2000. Effects of subsistence hunting on vertebrate community structure in Amazonian forests. Conservation Biology 14:240253.CrossRefGoogle Scholar
RIVERO, K., RUMIZ, D. I. & TABER, A. B. 2004. Estimating brocket deer (Mazama gouazoubira and M. americana) abundance by dung pellet counts and other indices in seasonal Chiquitano forest habitats of Santa Cruz, Bolivia. European Journal of Wildlife Research 50:161167.CrossRefGoogle Scholar
ROYLE, J. A. & NICHOLS, J. D. 2003. Estimating abundance from repeated presence-absence data or point counts. Ecology 84:777790.CrossRefGoogle Scholar
SALAS, L. A. & FULLER, T. K. 1996. Diet of the lowland tapir (Tapirus terrestris L) in the Tabaro River valley, southern Venezuela. Canadian Journal of Zoology 74:14441451.CrossRefGoogle Scholar
SCHOENER, T. W. 1974. Resource partitioning in ecological communities. Science 185:2739.CrossRefGoogle ScholarPubMed
STARK, M. A. 1986. Analysis of 5 natural soil licks, Benoue National-Park, Cameroon, West Africa. African Journal of Ecology 24:181187.CrossRefGoogle Scholar
TANKERSLEY, N. G. & GASAWAY, W. C. 1983. Mineral lick use by moose in Alaska. Canadian Journal of Zoology 61:22422249.CrossRefGoogle Scholar
TOBLER, M. W. 2008. The ecology of the Lowland Tapir in Madre de Dios, Peru: using new technologies to study large rainforest mammals. Ph.D. thesis, Texas A&M University, College Station, Texas, USA.Google Scholar
TOBLER, M. W., CARRILLO-PERCASTEGUI, S. E., LEITE PITMAN, R., MARES, R. & POWELL, G. 2008. An evaluation of camera traps for inventorying large- and medium-sized terrestrial rainforest mammals. Animal Conservation 11:169178.CrossRefGoogle Scholar
TRACY, B. F. & MCNAUGHTON, S. J. 1995. Elemental analysis of mineral lick soils from the Serengeti National Park, the Konza Prairie and Yellowstone National Park. Ecography 18:9194.CrossRefGoogle Scholar