Uso de espacios naturales y antropizados por el pecarí de collar (Dicotyles tajacu) en la estación biológica La Selva, Costa Rica
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El objetivo de esta investigación fue analizar el uso de espacios naturales y antropizados por el pecarí de collar (Dicotyles tajacu) en la Estación Biológica La Selva (EBLS), Costa Rica. Se registraron grupos e individuos de pecaríes mediante observaciones directas e indirectas, contando un total 170 individuos adultos y 30 crías (media = 3.62, DS = 4.04). El uso del espacio a nivel de sitio difirió del uso esperado (p < 0.000, X2 observado = 134.14, X2 acumulado = 22.36). La prueba de bondad de ajuste de chi-cuadrado mostró una fuerte evidencia de que no existe un uso proporcional con el área de las categorías (X2 = 832.30, df = 10, n = 76, P > 0.0001). Los intervalos de confianza de Bonferroni (IC 95%) evidenciaron mayor proporción de uso observado con respecto al esperado para las categorías agroforestería abandonada y área con infraestructura. Estas áreas son manejadas por la administración de la EBLS y existen árboles frutales, huertos, construcciones y mayor intensidad de uso público, por lo que para los pecaríes representan zonas de alimentación, refugio y descanso.
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Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-SinDerivadas 4.0.
Revista Mexicana de Mastozoología, nueva época por Instituto de Ecología, UNAM. Se distribuye bajo una Licencia Creative Commons Atribución-NoComercial-CompartirIgual 4.0 Internacional.
Basada en una obra en http://revistamexicanademastozoologia.com.mx/ojs/index.php/rmm.
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Agrawal, A. A., D.D., Ackerly, F. Adler, A.E. Arnold, C. Cáceres, D.F. Doak, E. Post, P.J. Hudson, J. Maron, K.A. Mooney, M. Power, D. Schemske, J. Stachowicz, S. Strauss, M.G. Turner y E. Werner. 2007. Filling key gaps in population and community ecology. Frontiers in Ecology and the Enviroment, 5:145–152. https://doi.org/10.1890/1540-9295
Alldredge, J. R. y J. Griswold. 2006. Design and analysis of resource selection studies for categorical resource variables. Journal of Wildlife Management, 70:337–346. https://www.jstor.org/stable/3803679
Armstrong, A. H., A. Huth, B. Osmanoglu, G. Sun, K.J. Ranson y R. Fischer. 2020. A multi-scaled analysis of forest structure using individual-based modeling in a Costa Rican rainforest. Ecological Modelling, 433: 109226. https://doi.org/10.1016/J.ECOLMODEL.2020.109226
Arroyo-Arce, S., L. Berrondo, Y. Canto, N. Carrillo, V.G. Carrillo, C. Loaiza, M. Méndez, D. Rivera y K. Unda. 2013. Uso de dos tipos de bosque por saínos (Pecari tajacu) en estación “la selva”, Costa Rica. Cultura Científica, 0:32–39. http://www.revistasjdc.com/main/index.php/ccient/article/view/215
Beck, H. 2005. Seed predation and dispersal by peccaries throughout the neotropics and its consequences: a review and synthesis. Pp. 77–115, en: Seed fate: predation, dispersal and seedling establishment. (Forget, P.M., Lambert, J.E., Hulme, P.E., y S. B. Vander Wall, eds.). CABI Publishing. Wallingford, United Kingdom.
Beck, H. 2007. Synergistic impacts of ungulates and falling palm fronds on saplings in the Amazon. Journal of Tropical Ecology, 23:599–602.
Bellantoni, E. S. y P.R. Krausman. 1993. Habitat Use by collared peccaries in an urban environment. The Southwestern Naturalist, 38:345-351. https://doi.org/10.2307/3671613
BiotasTM. 2004. Version 2.0a Help and manual. Ecological Software Solutions LLC. https://www.ecostats.com/Biotas
Briceño-Méndez, M., E. Naranjo, M. Altrichter y S. Mandujano. 2017. Availability of two species of fruits and their influence on the social structure of Tayassu pecari and Dicotyles tajacu. Therya, 8:193–198. http://132.248.10.25/therya/index.php/THERYA/article/view/450/pdf_175
Byers, J. A. y M. Bekoff. 1981. Social, spacing, and cooperative behavior of the collared peccary, Tayassu tajacu. Journal of Mammalogy, 62:767–785. https://doi.org/10.2307/1380598
Carrillo, E., G. Wong y J.C. Sáenz. 1999. Mamíferos de Costa Rica. Instituto Nacional de Biodiversidad, Costa Rica.
Clark, D. A., D.B. Clark y S.F. Oberbauer. 2013. Field-quantified responses of tropical rainforest aboveground productivity to increasing CO2 and climatic stress, 1997–2009. Journal of Geophysical Research: Biogeosciences, 118:783–794. https://doi.org/10.1002/JGRG.20067
Clark, D. B., y D.A. Clark. 1989. The Role of Physical Damage in the Seedling Mortality Regime of a Neotropical Rain Forest. Oikos, 55:225-230.
Cromsigt, J. P. G. M., H.H.T. Prins y H. Olff. 2009. Habitat heterogeneity as a driver of ungulate diversity and distribution patterns: interaction of body mass and digestive strategy. Diversity and Distributions, 15:513–522. https://doi.org/10.1111/J.1472-4642.2008.00554.X
de Cassia Bianchi, R., R. Calixto-Campos, N.L. Xavier-Filho, N. Olifiers, M.E. Gompper y G. Mourão. 2013. Intraspecific, interspecific, and seasonal differences in the diet of three mid-sized carnivores in a large neotropical wetland. Acta Theriologica , 59:13–23. https://doi.org/10.1007/S13364-013-0137-X
de Cassia Bianchi, R., y S.L. Mendes. 2007. Ocelot (Leopardus pardalis) predation on primates in Caratinga Biological Station, Southeast Brazil. American Journal of Primatology, 69:1173–1178. https://doi.org/10.1002/AJP.20415
de Cassia Bianchi, R., S.L. Mendes y P. de Marco Júnior. 2010. Food habits of the ocelot, Leopardus pardalis, in two areas in southeast Brazil. Studies on Neotropical Fauna and Enviroment, 45:111–119. https://doi.org/10.1080/01650521.2010.514791
Delibes, M., J. Calzada, C. Chávez, E. Revilla, B.A. Ribeiro, D. Prado, C. Keller y F. Palomares. 2011. Unusual observation of an ocelot (Leopardus pardalis) eating an adult Linnaeus’s two-toed sloth (Choloepus didactylus). Mammalian Biology, 76:240–241. https://doi.org/10.1016/J.MAMBIO.2010.08.006
Ellisor, J. E. y W.F. Harwell. 1969. Mobility and home range of collared peccary in Southern Texas. The Journal of Wildlife Management, 33:425-427. https://doi.org/10.2307/3799848
Falconi-Briones, F. A., E.J. Naranjo, R. Reyna-Hurtado, M. Spínola, P. Enríquez-Rocha y R.A. Medellín, R. 2022. Habitat use and activity patterns of ungulates in a tropical rainforest of southern México. Therya, 13:171–182. https://doi.org/10.12933/THERYA-22-1167
Ferreguetti, A. C., C.L. Davis, W.M. Tomas y H.G. Bergallo. 2018. Using activity and occupancy to evaluate niche partitioning: the case of two peccary species in the Atlantic Rainforest, Brazil. Hystrix, the Italian Journal of Mammalogy, 29:168–174. https://doi.org/10.4404/HYSTRIX-00068-2018
Fragoso, J. M. 1999. Perception of scale and resource partitioning by peccaries: behavioral causes and ecological implications. Journal of Mammalogy, 80:993–1003. https://doi.org/10.2307/1383270
Green, M. C., L.A. Harveson y L.E. Loomis. 2001. Habitat selection by collared peccaries in trans-pecos Texas. Southwestern Naturalist, 46:246–251. https://doi.org/10.2307/3672541
Hartshorn, G. S. 1983. Plants. Pp. 118–157, en: Costa Rican Natural History (D. Janzen, ed.).
Jolochin, G. 2014. Patrones de nerviación foliar en Myrtaceae de la Estación Biológica La Selva, provincia de Heredia, Costa Rica. Polibotanica, 38:95–111. http://sura.ots.ac.cr/local/
Jones, P. F., A.F. Jakes, A.C. Telander, H. Sawyer, B.H. Martin y M. Hebblewhite. 2019. Fences reduce habitat for a partially migratory ungulate in the Northern Sagebrush Steppe. Ecosphere, 10:e02782. https://doi.org/10.1002/ECS2.2782
Keuroghlian, A. y D.P. Eaton, D. P. 2008. Fruit Availability and Peccary Frugivory in an Isolated Atlantic Forest Fragment: Effects on Peccary Ranging Behavior and Habitat Use. Biotropica, 40:62–70. https://doi.org/10.1111/J.1744-7429.2007.00351.X
Keuroghlian, A., D.P. Eaton y W.S. Longland. 2004. Area use by white-lipped and collared peccaries (Tayassu pecari and Tayassu tajacu) in a tropical forest fragment. Biological Conservation, 120:411–425. https://doi.org/10.1016/J.BIOCON.2004.03.016
Kuprewicz, E. K. 2013. Mammal abundances and seed traits control the seed dispersal and predation roles of terrestrial mammals in a Costa Rican Forest. Biotropica, 45:333–342. https://doi.org/10.1111/BTP.12014
Latham, S. R., A.P.K. Sirén y L.R. Reitsma. 2023. Space use and resource selection of Wood Turtles (Glyptemys insculpta) in the northeastern part of its range. Canadian Journal of Zoology, 101:20–31. https://doi.org/10.1139/CJZ-2022-0052
Martínez-Gutiérrez, P. G., E. Martínez-Meyer, F. Palomares y N. Fernández. 2017. Niche centrality and human influence predict rangewide variation in population abundance of a widespread mammal: The collared peccary (Pecari tajacu). Diversity and Distributions, 24:103–115. https://doi.org/10.1111/DDI.12662
Mcclearn, D., J.P. Arroyo-Mora, E. Castro, R.C. Coleman, J.F. Espeleta, C. García-Robledo, A. Gilman, J. González, A.T. Joyce, E. Kuprewicz, J.T. Longino, N. Michel, C.M. Rodríguez, A. Romero, C. Soto, O. Vargas, A. Wendt, S. Whitfield y R.M. Timm. 2016. The caribbean lowland evergreen moist and wet forests. Pp. 527–587, en: Costa Rica ecosystems. (M. Kepelle, ed.). University of Chicago Press.
Méndez-Figueroa, M. 2014. Densidad, relación con la vegetación, daños a cultivos agrícolas e interacción humanos-saínos (Pecari tajacu) en la Estación Biológica y fincas aledañas. Tesis de maestría, Instituto Internacional de Conservación y Manejo de Vida Silvestre, Universidad Nacional.
Michel, N. L., T.W. Sherry y W.P. Carson. 2014. The omnivorous collared peccary negates an insectivore-generated trophic cascade in Costa Rican wet tropical forest understorey. Journal of Tropical Ecology, 30:1–11. https://doi.org/10.1017/S0266467413000709
Murray, J. L. y G.L. Gardner. 1997. Leopardus pardalis. Mammalian Species, 548:1–10. https://doi.org/10.2307/3504082/2600738
Naughton-Treves, L.., J.L. Mena, A. Treves, N. Alvarez y V.C. Radeloff. 2003. Wildlife survival beyond park boundaries: the Impact of slash-and-burn agriculture and hunting on mammals in Tambopata, Peru. Conservation Biology, 17:1106–1117. https://doi.org/10.1046/J.1523-1739.2003.02045.X
Neu, C. W., C.R. Byers y J.M. Peek. 1974. A technique for analysis of utilization-availability data. The Journal of Wildlife Management, 38:541-545. https://doi.org/10.2307/3800887
O’Brien, C. S., H.M. Boyd, P.R. Krausman, W.B. Ballard, S.C. Cunningham y J.C. de Vos. 2005. Influence of wildfire and coyote presence on habitat use by collared peccaries. Wildlife Society Bulletin, 33:865–875. https://doi.org/10.2193/0091-7648(2005)33
Ontiveros, T. Y., F.M. Cappa, C.M. Campos y S.M. Giannoni. 2021. Confirmación de la presencia de pecarí de collar (Pecari tajacu) en el Parque Provincial Ischigualasto (San Juan, República Argentina). Notas Sobre Mamíferos Sudamericanos, 01:001–006. https://doi.org/10.31687/SAREMNMS.2020.0.10
Oviedo- Pérez, P. 2008. Distribución espacial de tinámidos (TINAMIFORMES) en la Estación Biológica La Selva, Costa Rica. Uniciencia, 22:93–97. https://www.redalyc.org/articulo.oa?id=475948929011
Paine, C. E. T. y H. Beck. 2007. Seed predation by neotropical rain forest mammals increases diversity in seedling recruitment. Ecology, 88:3076–3087.
Raich, J. W., D.A. Clark, L. Schwendenmann y T.E. Wood. 2014. Aboveground tree growth varies with belowground carbon allocation in a tropical rainforest environment. PLOS ONE, 9:e100275. https://doi.org/10.1371/JOURNAL.PONE.0100275
Redfern, J. V., R. Grant, H. Biggs y W. M. Getz. 2003. Surface-Water constraints on herbivore foraging in the Kruger National Park, South Africa. Ecology, 84:2092–2107. https://doi.org/10.1890/01-0625
Regolin, A. L., L.G. Oliveira-Santos, M.C. Ribeiro y L.L. Bailey. 2021. Habitat quality, not habitat amount, drives mammalian habitat use in the Brazilian Pantanal. Landscape Ecology, 36:2519–2533. https://doi.org/10.1007/S10980-021-01280-0/FIGURES/4
Reyna-Hurtado, R., I. March, E. Naranjo y S. Mandujano. 2014. Pecaríes en México. Pp. 339–362, en: Ecología y manejo de fauna silvestre en México. (Valdez, R., y J.A. Ortega, eds.). Colegio de Postgraduados and New Mexico State University.
Reyna-Hurtado, R. y G.W. Tanner. 2005. Habitat preferences of ungulates in hunted and nonhunted areas in the Calakmul Forest, Campeche, Mexico. Biotropica, 37:676–685. https://doi.org/10.1111/J.1744-7429.2005.00086.X
Robinson, C., S. Saatchi, D. Clark, J.H. Astaiza, A.F. Hubel y T.W. Gillespie. 2018. Topography and three-dimensional structure can estimate tree diversity along a tropical elevational gradient in Costa Rica. Remote Sensing, 10:629. https://doi.org/10.3390/RS10040629
Roldán, A. I. y J.A. Simonetti. 2001. Plant-Mammal Interactions in Tropical Bolivian Forests with Different Hunting Pressures. Conservation Biology, 15:617–623.
Romero, A., B.J. O’Neill, R.M. Timm, K.G. Gerow y D. McClearn. 2013. Group dynamics, behavior, and current and historical abundance of peccaries in Costa Rica’s Caribbean lowlands. Journal of Mammalogy, 94:771–791. https://doi.org/10.1644/12-MAMM-A-266.1/2/JMAMMAL-94-4-771-FIG5.JPEG
Sowls, L. 1997. Javelinas and other peccaries: their biology, management, and use. 2da. ed., University Press, Texas, EE.UU. https://www.tamupress.com/9781623490089/javelinas-and-other-peccaries
Sunquist, M., y F. Sunquist. 2002. Wild cats of the world. University of Chicago Press, Chicago, and London
Tejeda-Cruz, C., E.J. Naranjo, A.D. Cuarón, H. Perales y J.L. Cruz-Burguete. 2009. Habitat use of wild ungulates in fragmented landscapes of the Lacandon Forest, Southern Mexico. Mammalia, 73:211–219. https://doi.org/10.1515/MAMM.2009.044/MACHINEREADABLECITATION/RIS
Torrealba-Suárez, I. M. 1993. Ecología de los Grupos de sainos (Tayassu tajacu) y daños que ocasionan en los cultivos vecinos a La Estación Biológica La Selva, Costa Rica. Tesis de maestría, Instituto Internacional de Conservación y Manejo de Vida Silvestre, Universidad Nacional.