Effects of black howler monkey (Alouatta caraya) seed ingestion on insect larvae

Fig (Ficus monckii) and laurel (Ocotea puberula) seeds were obtained from Alouatta caraya feces (ingested seeds) and from trees (noningested) in northeastern Argentina. Seeds were examined to detect the presence (infested) or absence (noninfested) of larvae. Sixty percent (N = 315) of noningested fig seeds were galls with insect larvae inside, while 23% (N = 331) were encountered in the ingested group. Eighty-two percent (N = 28) of noningested laurel seeds were infested, and only 19% (N = 63) of ingested seeds were infested. According to the present data, the insects' larvae are digested by howlers intaking animal protein, but the laurel seeds were not destroyed. Am. J. Primatol. 45:411–415, 1998. © 1998 Wiley-Liss, Inc.     

Current status of the habitat and population of the black howler monkey (Alouatta pigra) in Balancán, Tabasco, Mexico

We evaluated the habitat and populations of the black howler monkey (Alouatta pigra) in the municipality of Balancán, Tabasco, southeastern Mexico, using a combination of field surveys and remotely sensed data. We identified 21,937 ha of remnant vegetation composed of 1,348 fragments. Fragments separated by up to 200 m were grouped into \"clusters\" of fragments in accordance with the maximum observed open distance crossed by A. pigra. A total of 11% or 84 of the 772 clusters identified through remote sensing were selected at random, and for these we determined the vegetation type, canopy height, area, and distance to the closest human settlement. In these same 84 clusters, which included a total area of 9,817 ha, from October to June of 2006 we located a total of 1,064 black howler monkeys, including 228 troops and 49 solitary monkeys. A. pigra was found in 62 (74.7%) of all clusters visited, with a cumulative area of 6,032 ha. Troops varied in size from 2 to 15 individuals (average 6.0+/-2.9 ind/troop). Adults were 67% (n=716) of detected individuals, whereas juveniles were 20.5% (n=218) and infants were 12.5% (n=133). We found black howlers to occur at an ecological density of 10.8 ind/km(2), which is low in comparison with A. pigra in other fragmented and conserved sites. We found a statistically significant relationship between the area of clusters and the abundance of howler monkeys (r(2)=0.2, F=10.47, gl=3, P=0.002). In addition, the probability of finding A. pigra was greater in secondary vegetation, riparian vegetation, tropical dry forest, undisturbed tropical oak forest, and palm forest (F=12, gl=3, P<0.0001), as compared with disturbed tropical oak forest. Our results provide data on the distribution, abundance, and population structure of black howler monkeys in a fragmented landscape in the southeast of Mexico. These data are a necessary prerequisite for conservation planning for this species.     

Effects of forest fragmentation on the physiological stress response of black howler monkeys

Habitat loss and fragmentation can create severe environmental problems for forest species, and may ultimately lead to local population extinction. One mechanism that might play a role in this process is the physiological stress response of individuals, because animals that experience chronic stress might show reduced rates of reproduction and survival. In this study, we investigated whether black howler monkeys Alouatta pigra inhabiting forest fragments experienced greater physiological stress than those in continuous forest. Faecal cortisol metabolite levels were compared between monkeys inhabiting fragmented and continuous forests in Southern Mexico. The sex of the animals was taken into consideration, while activity patterns and aggressive events were also recorded to examine differences in behaviour and sociality. A chemiluminescent enzyme immunoassay was utilized to determine faecal cortisol metabolite levels. Our results showed that cortisol metabolite levels were higher in howler monkeys from forest fragments, and that they vary through time. Patterns of locomotion also differed between forest types, as monkeys from fragments travelled at higher frequencies, while monkeys from continuous forests performed more of their movements within tree crowns. There was no difference in the frequency of feeding, resting and social interactions between fragmented and continuous forest monkeys. Higher faecal cortisol metabolite levels in fragmented areas are likely the result of suboptimal environments and could have long-term adverse effects on monkey health, fertility and survival. We propose that faecal cortisol metabolite measurements can be a useful conservation tool for monitoring populations of long-lived species subsisting under suboptimal conditions.     

Predation by jaguar on howler monkeys (Alouatta seniculus) in Venezuela

We document the loss of all but the youngest member of a troop of six howler monkeys due to probable jaguar predation during a 7-month period in 1988. The formation of Guri Lake resulted in forest fragmentation which forced monkeys into new and unfamiliar areas and altered the balance of predator and prey populations, and may thus have contributed indirectly to the success of the jaguar. The selection of defoliated (dead) trees for sleeping sites by the howlers may have directly increased the risk of predation. © 1992 Wiley-Liss, Inc.     

Red howler monkey birth data I: Seasonal variation

A large set of birth data from a population of red howler monkeys (Alouatta seniculus) in two habitats found a consistent birth “dip,” with births occurring less frequently in early wet season (May–July) than during the remaining months. In one of two habitats, births were negatively correlated with rainfall, and viable conceptions were positively correlated with rainfall. The observed degree of within-troop birth synchrony appeared to reflect populational synchrony with environmental factors. Correlations between births and the phenology of plant foods were not striking, but there was weak support for the hypothesis that births are timed to maximize the availability of weaning foods. Reduced births in early wet season also minimize the number of Infants who would experience the transition to independent locomotion and feeding during the peak of the dry season when probable low moisture content of foods and high daytime temperatures might be disadvantageous. However, there was no relationship between season of birth and infant mortality.     

Grooming in brown howler monkeys,Alouatta fusca

The grooming behavior of a group of brown howler monkeys was studied for one year in an Atlantic forest reserve of southeastern Brazil. A total of 290 grooming bouts were recorded and analyzed. The two adult females directed most of the grooming (91%), while the adult male was the major recipient (37%). Grooming between females, and between them and their siblings, also occurred quite often. On average, the group spent 2% of its daily time grooming, with a higher frequency around noon. There were significant differences, however, in time spent grooming between seasons; grooming was more abundant during the coldest seasons (autumn–winter) and rarer in hotter ones (spring–summer). A significant negative correlation was found between grooming time and temperature, but contrary to expectations, grooming time failed to correlate with both the group' diet and the demands of food-gathering, as measured by travelling time and day range length. A comparison of grooming behavior with other species of the genus suggests that brown, red (A. seniculus), and black howler monkeys (A. caraya) are more similar to each other than to mantled howlers (A. palliata), a result that probably is linked with the differing social structure and group size of the latter species. © 1995 Wiley-Liss, Inc.     

Red howler monkey birth data II: Interannual,habitat, and sex comparisons

Data presented in this paper are derived from the births and subsequent histories of red howler infants born in two habitats. Overall the sex ratio of infants at birth was about 1:1. Infant survivorship (at 1 yr) was about 80%, and 44% of infant mortality was attributed to infanticide by males. Survivorship curves indicated a dramatic sex difference, with far fewer females than males known to be alive at age 7 yr. However, this sex difference may be inflated because emigrant males are more easily identified than emigrant females, and females may be dispersing beyond the boundaries of the study area at a higher rate. Annual birthrate varied somewhat from year to year and was positively related to rainfall. Annual birthrate tended to be higher in the habitat with lower density and higher growth rate. Consistent with the trends, in annual birthrate, variation in interbirth interval length (TBR after births of surviving infants was related primarily to habitat differences and annual variation in rainfall. Season of birth and maternal age class had no effect on IBI. Infant sex had mostly nonsignificant effects on IBI. A small sample indicated that IBI's were significantly longer after the births of females who eventually became natal breeders than after the births of females who eventually emigrated. This difference might reflect differential parental (maternal) investment of some sort.     

Fecundity in the captive howler monkey,Alouatta caraya

Seven female Black howler monkeys, Alouatta caraya, from both wild- and captive-born origins have reproduced at Riverbanks Zoological Park. Three of the five wild-born females arrived as juveniles and grew to maturity; the other two were already mature upon arrival and reproduced shortly therafter. Two females which were born within the park's collection have since reached maturity and also reproduced. The interval between the first and second young of wild-born howlers is longer than between subsequent birth intervals. Subsequent young are also more precocious than their preceding siblings. In at least one case, a socially inferior female did not reproduce until placed within a different troop situation which elevated her social status. Females born in captivity conceived when 42 and 35 months old, the former situation being linked to low social status. Young born to females housed under both seasonal and regulated conditions of photoperiod demonstrated no difference in breeding intervals and seasonality of birth does not appear to be a factor in howler monkey reproduction.     

Howler monkey tolerance to habitat shrinking: Lifetime warranty or death sentence?

Habitat loss and fragmentation are major threats to the conservation of nonhuman primates. Given that species differ in their responses to fragmented landscapes, identifying the factors that enable them to cope with altered environments or that cause their extirpation is critical to design conservation management strategies. Howler monkeys (Alouatta spp.) are good models for studying the strategies of tolerant arboreal taxa and how they cope with spatial restriction, because they live in habitats ranging from vast pristine forests to small disturbed fragments and orchards. While some aspects of their ecology and behavior are conserved, others vary in predictable ways in response to habitat shrinking and decreasing resource availability. We argue that the ability of individual howler monkeys to inhabit low-quality environments does not guarantee the long-term persistence of the small populations that live under these conditions. Their local extirpation explains why few forest fragments below a given area threshold are frequently inhabited in landscapes where recolonization and gene flow are compromised by long isolation distances or less permeable matrices. In sum, howlers’ ability to cope with habitat restriction at the individual level in the short-term may mask the inevitable fate of isolated populations, thereby compromising the persistence of the species at a regional scale in the long-term if howlers’ need for protection in large forests is undervalued.     

A study of a black howling monkey (Alouatta caraya) population in northern Argentina

A population of Alouatta caraya in northern Argentina had an ecological density of 130 animals per km². Mean troop size varied from 7.2 to 8.9 individuals, and the ratio of adult males to adult females from 0.58 to 0.51. Infants comprised from 6% to 14% of the population, juveniles from 16% to 21%. These percentages probably vary seasonally in response to a birth peak at the beginning of the dry season. Males were age-graded in multi-male troops. Sexual dimorphism was extreme in this species. Males were all black and averaged 6.7 kg; females were yellow-brown and averaged 4.4 kg. Juvenile males retained the pelage color of the female until approximately 4.5 yr of age and 5 kg in weight. No genital mimicry or exaggeration occurred in this species. Vocalizations of A. caraya were similar to those of A. seniculus, both of which tend to be lower pitched than those of A. palliata.