O cuidado parental é conhecido por impor um elevado custo energético às fêmeas primatas, pois, além da lactação, muitas mães primatas também provêm transporte aos filhotes. Diversos estudos têm documentado o elevado custo energético da lactação, no entanto, pouco se sabe sobre o custo energético para o transporte do filhote e seus efeitos na recuperação da condição física das mães. Nós comparamos as atividades de fêmeas muriquis (Brachyteles hypoxanthus Kuhl, 1820), durante um período de 12 meses, na RPPN Feliciano Miguel Abdala, Minas Gerais Brasil, a fim de investigar se as mães durante o ano de desmame dos filhotes se comportavam diferentemente das mães no ano pós-desmame, quando elas recomeçaram o ciclo reprodutivo e de cópulas, e quando estavam concebendo novamente. Nós não encontramos nenhuma diferença significativa no orçamento das atividades comportamentais entre as mães no ano de desmame (n = 4) versus mães no ano pós-desmame (n = 5), apesar das mães no ano de desmame terem gasto significativamente mais tempo em proximidade com seus infantes e carregado seus infantes do que as mães no ano pós-desmame. Nós sugerimos que, em fêmeas muriquis, o orçamento de energia do desmame é similar ao de pós-desmame.

Infant care is known to impose high energetic costs on female primates because in addition to lactation, most primate mothers also provide transport for their offspring. Many studies have documented the high energetic costs of lactation, but less is known about energetic costs of infant carrying and their effects on the recovery of maternal physical condition. We compared the activities of female northern muriquis (Brachyteles hypoxanthus Kuhl, 1820) over a 12-month period at the RPPN Feliciano Miguel Abdala, Minas Gerais, Brazil to investigate whether mothers during their weaning year behaved differently than mothers in their post-weaning year, when they resumed reproductive cycling and copulating, and conceived again. We found no significant differences in the behavioral activity budgets of mothers in their weaning year (n = 4) versus post-weaning year (n = 5), despite the significantly higher proportion of time that mothers in their weaning year spent in close proximity with their infants and carrying their infants compared to mothers in their post-weaning year. We suggest that the energy budgets of weaning are similar to those of post-weaning in female northern muriquis.

We assessed the genetic diversity of two northern muriqui (Brachyteles hypoxanthus Primata, Atelidae) populations, the Feliciano Miguel Abdala population (FMA, n = 108) in the Brazilian state of Minas Gerais (19°44' S, 41°49' W) and the Santa Maria de Jetibá population (SMJ, n = 18) in the Brazilian state of Espírito Santo (20°01' S, 40°44' W). Fecal DNA was isolated and PCR-RFLP analysis used to analyze 2160 bp of mitochondrial DNA, made up of an 820 bp segment of the gene cytochrome c oxidase subunit 2 (cox2, EC 1.9.3.1), an 880 bp segment of the gene cytochrome b (cytb, EC 1.10.2.2) and 460 bp of the hypervariable segment of the mtDNA control region (HVRI). The cox2 and cytb sequences were monomorphic within and between populations whereas the HVRI revealed three different population exclusive haplotypes, one unique to the SMJ population and two, present at similar frequencies, in the FMA population. Overall haplotype diversity (h = 0.609) and nucleotide diversity (pi = 0.181) were high but reduced within populations. The populations were genetically structured with a high fixation index (F ST = 0.725), possibly due to historical subdivision. These findings have conservation implications because they seem to indicate that the populations are distinct management units.

The muriqui (Brachyteles) is one of the most endangered primates in the world, however little is known about the viability of the remaining populations. We evaluated the technique of extracting DNA from wild muriqui feces for PCR applications. In order to determine the effect of the DNA in subsequent amplifications, we analyzed five different extracts. The importance of the recommended BSA and the HotStarTaq DNA polymerase was tested. The minimal conditions to successfully amplify highly degraded fecal DNA were determined, showing that the recommended reagents are not required. We envision that this method may be useful in further conservation management studies.