Toque macaque

Abstract: Human and great ape milks contain a diverse array of milk oligosaccharides, but little is known about the milk oligosaccharides of other primates, and how they differ among taxa. Neutral and acidic oligosaccharides were isolated from the milk of three species of Old World or catarrhine monkeys (Cercopithecidae: rhesus macaque (Macaca mulatta), toque macaque (Macaca sinica) and Hamadryas baboon (Papio hamadryas)) and three of New World or platyrrhine monkeys (Cebidae: tufted capuchin (Cebus apella) and Bolivian squirrel monkey (Saimiri boliviensis); Atelidae: mantled howler (Alouatta palliata)). The milks of these species contained 6–8% total sugar, most of which was lactose: the estimated ratio of oligosaccharides to lactose in Old World monkeys (1:4 to 1:6) was greater than in New World monkeys (1:12 to 1:23). The chemical structures of the oligosaccharides were determined mainly by 1H-NMR spectroscopy. Oligosaccharides containing the type II unit (Gal(β1-4)GlcNAc) were found in the milk of the rhesus macaque, toque macaque, Hamadryas baboon and tufted capuchin, but oligosaccharides containing the type I unit (Gal(β1-3)GlcNAc), which have been found in human and many great ape milks, were absent from the milk of all species studied. Oligosaccharides containing Lewis x (Gal(β1-4)[Fuc(α1-3)]GlcNAc) and 3-fucosyl lactose (3-FL, Gal(β1-4)[Fuc(α1-3)]Glc) were found in the milk of the three cercopithecid monkey species, while 2-fucosyl lactose (5'-FL, Fuc(α1-2)Gal(β1-4)Glc) was absent from all species studied. All of these milks contained acidic oligosaccharides that had N-acetylneuraminic acid as part of their structures, but did not contain oligosaccharides that had N-glycolylneuraminic acid, in contrast to the milk or colostrum of great apes which contain both types of acidic oligosaccharides. Two GalNAc-containing oligosaccharides, lactose 3′-O-sulfate and lacto-N-novopentaose I (Gal(β1-3)[Gal(β1-4)GlcNAc(β1-6)]Gal(β1-4)Glc) were found only in the milk of rhesus macaque, hamadryas baboon and tufted capuchin, respectively. Further research is needed to determine the extent to which the milk oligosaccharide patterns observed among these taxa represent wider phylogenetic trends among primates and how much variation occurs among individuals or species.

Abstract: Based on study of 116 museum specimens and review of relevant literature, a new species account ofMacaca sinica, the Sri Lanka toque macaque, is presented. External and cranial characters of the species are described and analyzed. A summary of natural history of the species includes information on habitats, arboreal-terrestrial preferences, predators, diet, relations with other primate species, density, troop size and composition, home range area, and reproductive biology. Two subspecies ofM. sinica are recognized, northernM. s. sinica (Linnaeus, 1771) and southwesternM. s. aurifrons (Pocock, 1931). Geographic ranges of these two subspecies meet in a 50–200 km broad contact zone in which representatives of both subspecific phenotypes are encountered (35s. sinica phenotypes; 8s. aurifrons phenotypes in 43 contact zone specimens examined). An annotated gazetteer of known macaque localities in Sri Lanka provides information concerning available museum specimens and field reports by collectors or observers. Comparative study of three remaining species in thesinica group (M. radiata, M. assamensis, & M. thibetana) is in progress.

Abstract: The occurrence of four parasitic species of zoonotic potential, Entamoeba coli , Entamoeba histolytica / dispar , Trichuris sp. and hookworm was investigated in the toque macaque, grey langur and the purple-faced langur at 32 sites across Sri Lanka. The study was carried out during the rainy season months of February - March in both 2007 and in 2009 and in December of 2010. 93 faecal samples were collected from 49 monkey troops at representative locations in altitudinal /climatic zones across the country where toque macaques (58 samples), grey langurs (21 samples) and purple-faced langurs (14 samples) naturally occur. Overall, the most common parasitic species found in all three primates were Trichuris sp. (28 %) and E. coli (25 %). Notably, hookworms were present in 23 % of the grey langur samples and 33 % of the toque macaque samples but absent in the purple-faced langur samples collected. Statistically significant variability in the prevalence levels across altitudinal/climatic zones was noted for toque macaques. Overall, group prevalence values in toque macaques decreased with increasing altitude; the highest values were found in the intermediate to arid lowland zones, and were lowest in the upland wet zone. Only Trichuris sp. and hookworm were found (13 %, 7 %, respectively) in the highland/ wet zone. Molecular analysis will be necessary to genetically type the parasite species before drawing firm conclusions about the status of zoonotic transmission between humans and non-human primates in the country. However this study highlights the need to systematically survey the human parasite population in areas where primates are commonly found to harbour these parasite species. J.Natn.Sci.Foundation Sri Lanka 2013 41 (4):319-326 DOI: http://dx.doi.org/10.4038/jnsfsr.v41i4.6246

Abstract: Sri Lanka is a biodiversity hotspot with high human density that contributes to increasing human-monkey conflict (HMC). In 50 years of primate studies there, the development of HMC has been documented, and many workshops and interventions organized to ameliorate HMC. These activities prompted the present survey. In the extensive lowland dry zone of Sri Lanka, the affected nonhuman primates are the toque macaque, gray and purple-faced langurs and slender loris. We surveyed and evaluated the attitudes of rural residents towards these four species in an effort to contribute to an ethnoprimatological approach to conservation, i.e., promote a coexistence and sharing of habitat between humans and monkeys. We selected 13 villages near Polonnaruwa, located centrally in the dry zone. The four nonhuman primate species differ in their behavioral ecologies, and this influenced how frequently they were thought of as pests. Most HMC was with the macaque and gray langur, less with the purple-faced langur and least with the loris. The underlying sentiment among stakeholders towards monkeys was generally either neutral or positive. Nonetheless, the majority (80%) of people desired a translocation of the troublesome monkeys from their properties to protected areas, which is impractical. Few (< 1%) openly wanted monkeys destroyed. While a traditional reverence for monkeys provides a solid basis for science and media-based education, it also contributes to the feeding of monkeys and consequent unnatural population growth, and enhanced HMC. Public understanding of the underlying causes of HMC was poor, hindering effective solutions. A combination of a feeding ban, possibly contraceptive intervention at localized HMC trouble spots, and extensive education may be the only benign alternatives to the destruction of wild primates by a powerful minority. Coexistence through strengthening and expansion of exclusive suitable protected habitats for all wildlife is a priority.