Influence of Fruit Availability on Ecological Overlap among Four Neotropical Primates at Tinigua National Park, Colombia 1

By P. Stevenson, M. Quinones, Jorge A. Ahumada. 2000

212 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Social Psychology

View Paper: https://www.semanticscholar.org/paper/cd4ab8036b3e42733055863aebb5e5f12ea377d0

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Citations in the corpus

A Multi-Forest Comparison of Dietary Preferences and Seed Dispersal by Ateles spp (2005, methodology): “We calculated preferences for Yasuni per both Dew (2001) and Suarez (2003) by averaging the preference index for a genus when it was consumed in both studies, or, for genera only consumed in one study, by using the preference index from that study.”
Flowering Patterns in a Seasonal Tropical Lowland Forest in Western Amazonia (2008, methodology): “In some potentially ambiguous cases additional observations from botanical vouchers and studies on primate diets were used as well (Stevenson et al. 2000a,b; Stevenson 2006).”
Effects of Seed Dispersal by Three Ateline Monkey Species on Seed Germination at Tinigua National Park, Colombia (2002, background): “Howlers (Alouatta spp.) rely more on foliage than the other members of the clade do and may eat only leaves during some periods of the year (Stevenson et al., 2000a).”
Use of Mineral Licks by White-Bellied Spider Monkeys (Ateles belzebuth) and Red Howler Monkeys (Alouatta seniculus) in Eastern Ecuador (2010, background): “(Campbell et al. 2005; De Souza et al. 2002; Dew 2005; Izawa 1993; Izawa and Lozano 1990; Stevenson et al. 2000 ).”
Foraging, Food Choice, and Food Processing by Sympatric Ripe-Fruit Specialists: Lagothrix lagotricha poeppigii and Ateles belzebuth belzebuth (2005, background): “They are diurnal canopy dwellers weighing approximately 6–8 kg and are ripe-fruit specialists, feeding primarily on fleshy fruit pulp, supplemented with young leaves, insects, and other foods (Ahumada, 1989; Cant, 1977, 1990; Castellanos and Chanin, 1996; Chapman, 1987, 1988; Defler and Defler, 1996”
Diet and Food Choice in Peruvian Red Uakaris (Cacajao calvus ucayalii): Selective or Opportunistic Seed Predation? (2011, background): “The diets of sympatric primates typically overlap considerably when ripe fruit pulp is abundant, and it is during periods of relative ripe fruit pulp scarcity that the diets of sympatric species differentiate (Stevenson et al. 2000; Terborgh 1983; Tutin et al. 1997).”
Diet, Habitat Selection and Natural History of Cacajao melanocephalus ouakary in Jaú National Park, Brazil1 (2005, background): “Seasonally-fluctuating levels of competition have been demonstrated for many other taxa (invertebrates: Vasquez et al., 1984; fish: Bouton et al. 1997; amphibians: Lynch, 1985; lizards: Lister, 1981; birds: Rosenberg et al., 1982; rodents: Llewellyn and Jenkins, 1987; bats: Heithaus et al., 1975; an”
Diets of Howler Monkeys (2015, background): “Howlers have been observed ingesting soil from the forest fl oor (from “barreiros” or “salados”: Izawa 1993 ; Stevenson et al. 2000 , 2002 ; Blake et al. 2010 ), bird nests ( Bicca-Marques and Calegaro-Marques 1994a, b, c ), and termitaria (Julliot and Sabatier 1993 ; de Souza et al. 2002 ).”
Diet and Feeding Ecology of Ateles chamek in a Bolivian Semihumid Forest: The Importance of Ficus as a Staple Food Resource (2008, background): “Virola produce lipid-rich fruit that feature prominently in diets of Ateles spp. (Dew 2005; Russo et al. 2005; Stevenson et al. 2000; van Roosmalen 1985).”
The relationship between fruit production and primate abundance in Neotropical communities (2001, unknown): “…used by the monkeys, except for seven sites,basal area of plants that are almost exclusively conwhere I used vegetation plots of forested areas rel-sumed by birds, fish or bats (Appendix 2, based on van atively nearby (<100 km), within the same rainfall andRoosmalen, 1985a; Stevenson et al., 2000).”