Since 1982, we have studied the behavior and ecology of one group of muriquis inhabiting an 800 hectare forest in Minas Gerais, Brazil. This is the only ongoing long-term field study of this highly endangered primate. We have described the muriqui's unusual egalitarian society and pattern of female-biased dispersal and male philopatry while documenting the effects of seasonal changes in food availability on diet. Demographic records of recognized individuals have yielded the only data on basic life history variables, including age at first reproduction and interbirth intervals for this species. Correlations between reproductive events and ecological variables indicate pronounced reproductive seasonality, suggesting that components of muriqui diets may regulate their fertility. Dietary components may also link to the regulation of intestinal parasite infections. Brazilian and American collaborators are identifying muriqui parasites and analyzing plant foods for anthelminthic and phytosteroid activity. Long-term demographic and ecological data have provided the basis for a population viability analysis and recommendations for the conservation of this endangered primate. New collaborations are exploring the comparative behavioral ecology of the other sympatric primates at this site to understand the effects of life histories on reproduction and population dynamics. RESULTS Key accomplishments included insights into muriqui mating preferences and the inte-gration of muriqui behavioral ecology and conservation biology. Analyses of female sexual behavior and fecal steroid assays also provided key insights into the reproductive ecology of female muriquis. OBJECTIVE: To understand the interrelationships among behavior, ecology, and reproduction in wild muriquis (Brachyteles arachnoides) in a seasonal Atlantic forest fragment. FUTURE DIRECTIONS To continue to monitor the effects of demographic changes on the behavioral and reproductive ecology of this muriqui population. KEY WORDS reproduction, parasites, fertility 1997

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-38
Application #
6277715
Study Section
Project Start
1998-05-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
38
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Kang, HyunJun; Mesquitta, Walatta-Tseyon; Jung, Ho Sun et al. (2018) GATA2 Is Dispensable for Specification of Hemogenic Endothelium but Promotes Endothelial-to-Hematopoietic Transition. Stem Cell Reports 11:197-211
Rhoads, Timothy W; Burhans, Maggie S; Chen, Vincent B et al. (2018) Caloric Restriction Engages Hepatic RNA Processing Mechanisms in Rhesus Monkeys. Cell Metab 27:677-688.e5
Ellis-Connell, Amy L; Balgeman, Alexis J; Zarbock, Katie R et al. (2018) ALT-803 Transiently Reduces Simian Immunodeficiency Virus Replication in the Absence of Antiretroviral Treatment. J Virol 92:
Park, Mi Ae; Jung, Ho Sun; Slukvin, Igor (2018) Genetic Engineering of Human Pluripotent Stem Cells Using PiggyBac Transposon System. Curr Protoc Stem Cell Biol 47:e63
Ellis, Amy; Balgeman, Alexis; Rodgers, Mark et al. (2017) Characterization of T Cells Specific for CFP-10 and ESAT-6 in Mycobacterium tuberculosis-Infected Mauritian Cynomolgus Macaques. Infect Immun 85:
Rodrigues, Michelle A (2017) Female Spider Monkeys (Ateles geoffroyi) Cope with Anthropogenic Disturbance Through Fission-Fusion Dynamics. Int J Primatol 38:838-855
Buechler, Connor R; Bailey, Adam L; Lauck, Michael et al. (2017) Genome Sequence of a Novel Kunsagivirus (Picornaviridae: Kunsagivirus) from a Wild Baboon (Papio cynocephalus). Genome Announc 5:
Wu, Hong; Whritenour, Jessica; Sanford, Jonathan C et al. (2017) Identification of MHC Haplotypes Associated with Drug-induced Hypersensitivity Reactions in Cynomolgus Monkeys. Toxicol Pathol 45:127-133
Shackman, A J; Fox, A S; Oler, J A et al. (2017) Heightened extended amygdala metabolism following threat characterizes the early phenotypic risk to develop anxiety-related psychopathology. Mol Psychiatry 22:724-732
Kalin, Ned H (2017) Mechanisms underlying the early risk to develop anxiety and depression: A translational approach. Eur Neuropsychopharmacol 27:543-553

Showing the most recent 10 out of 528 publications