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Comparative studies of subspecies under different ecological environments offer insights into intraspecies evolutionary adaptive mechanisms. Golden snub-nosed monkeys (Rhinopithecus roxellana) include three subspecies in China classified mainly by their morphological variations: R. r. roxellana (Sichuan and Gansu province), R. r. qinlingensis (Shaanxi province) and R. r. hubeiensis (Hubei province). These three subspecies live in three isolated area with different environments. Past works focused on the last two subspecies, but little information of habitat and behaviors of the nominated subspecies (R. r. roxellana) is available to date. We conducted a two-year study on the diet, activity budget, home range and social organization of 4 herds of R. r. roxellana, based on a total of 106 days' observation in Laohegou (LHG) Nature Reserve, Sichuan province. By using scan sampling method, our results suggest that the R. r roxellana feeds predominantly on leaves (77.5%), and spends more time feeding (40.0%) and resting (27.0%) while compared to the other two subspecies. Kernel Density Estimation Method based on GPS technology confirms that R. r roxellana has relatively larger home ranges (49.1 km 2 ). The unit size (8.3 ± 3.5 individuals) of R. r roxellana is also smaller. Therefore, it is possible that differences in food availability in relation to habitats have important impacts on the feeding strategy and social system of the golden snub-nosed monkey. These results provide data to further explore intraspecific adaptations of living primates.

Rapid global deforestation has forced many of the world's primates to live in fragmented habitats, making the understanding of their behavioral responses to degraded and fragmented habitats a key challenge for their future protection and management. The black-and-white snub-nosed monkey (Rhinopithecus bieti) is an endangered species endemic to southwest China. The forest habitat ranges from near-continuous to fragmented. In this study, we investigated the activity budget and diet of a R. bieti population that live in an isolated and degraded habitat patch at Mt. Lasha in Yunnan Province, near the current southern limit of the species. We used our data along with data from six other sites in more-continuous habitats across its range to model factors that predict stress, including feeding effort and time feeding on lichens against potential predictive parameters. Models showed feeding effort across all sites increased with increasing altitude and latitude, and with decreasing food species diversity. There was also a strong positive relationship between feeding effort and time feeding lichens. The Mt. Lasha R. bieti population exploited a total of 36 food species, spending 80.2% of feeding time feeding on lichens, Bryoria spp. and Usnea longissima. These figures are more comparable to those living in the north than those living in the mid- and southern part of the species' range. Given the models for feeding effort and time feeding on lichens, the unexpectedly high time spend feeding on lichens and feeding effort relative to latitude and elevation are suggestive of a stressed population at Mt. Lasha.

Golden snub-nosed monkey (Rhinopithecus roxellana) is one of the most endangered primate species found in China, exhibiting multilevel society consisting of several one-male-females together with their offspring units (OMU), and all-male units (AMU). Female dispersal patterns of the species within herd have been well documented, whereas those of the males within or between herds are still poorly understood. Our results based a long-term observation indicate that more than half of sub-adult males, and half of the deposed males that stayed a short period in OMU disperse between herds, three of them established their own OMU in new herd after the dispersal. Smaller number of the sub-adult and adult males, compared with adult females, stayed in natal herd, implying sub-adult males started dispersing and male-biased dispersal occurred between herds. High frequencies of resident males were wounded as their OUMs were taken over, and resident males co-operation defend bachelor males were found. Mating competition among males within the herd may have contributed to the scenarios of male-biased dispersal. The results also suggest that maintaining connection between isolated herds and establishing the corridors among the fragmented habitats for the species will greatly benefit increasing its gene flow and promoting conservation status.

Seasonal variation in environmental factors is vital to the regulation of seasonal reproduction in primates. Consequently, long-term systematic data is necessary to clarify the birth seasonality and pattern of primates in highly seasonal environments. This study indicated that black-and-white snub-nosed monkeys (Rhinopithecus bieti) at Mt. Lasha exhibited strict birth seasonality with a pulse model. Infants were born with a certain degree of synchronization. Birth distribution showed three birth peaks, and the birth pattern showed a "V" style in even-numbered years and a gradual increase in odd-numbered years. The beginning date, end date and median birth date were earlier in even-numbered years than those in odd-numbered years. The higher latitude of their habitats, earlier birth date, shorter birth period, fewer birth peaks and stronger birth synchrony might be adaptations for strongly seasonal variation in climate and food resources. After the summer solstice when daylight length began to gradually shorten, R. bieti at Mt. Lasha started to breed during the period with the highest environmental temperature and food availability, which implied that photoperiod may be the proximate factor triggering the onset of estrus and mating. It appears that R. bieti coincided conception and mid-lactation with the peak in staple foods, and weaning with the peak in high quality of foods. Thus, food availability was the ultimate factor regulating reproductive seasonality, and photoperiod was the proximate factor fine-turning the coordination between seasonal breeding and food availability.

There exists very limited information on the set of scavengers that feed on the carcasses of wild primates. Here, we describe, based on information collected using a remote camera trap, carnivores consuming/scavenging the carcass of a wild golden snub-nosed monkey (Rhinopithecus roxellana) in the Laohegou Nature Reserve, Sichuan, China. During a 3 month behavioral and ecology study of a band of golden snub-nosed monkeys (March through May 2013), we encountered the carcass of an adult male (male golden snub-nosed monkeys weigh approximately 12-16 kg). After examining the dead monkey, we returned it to the death site and set out a camera trap to record the behavior and identity of scavengers. Over the course of 25 days, we collected 4145 photographs taken by the camera trap. Scavengers identified from these photographs include a masked civet (Paguma larvata), Asiatic black bear (Ursus thibetanus), large-billed crow (Corvus macrorhynchos) and the chestnut rat (Rattus fulvescens). No member of the golden snub-nosed monkey's social group, which was composed of approximately 120 individuals, was found to return to the general area of the death site. The masked civet fed principally on the face and intestines of the corpse at night, while the black bear consumed most of the body of the dead monkey during both the daytime and nighttime. These two taxa consumed virtually the entire carcass in one week. We suggest that the use of camera traps offers a powerful research tool to identify the scavenger community of a given ecosystem.

Black-and-white snub-nosed monkeys (Rhinopithecus bieti) inhabit one of the harshest habitats by any nonhuman primate. Reliable predictive cues to initiate reproduction may be particularly critical for R. bieti because they inhabit such seasonally energetically challenging environments. To better understand the seasonal distribution of and predictive cues to reproduction, we collected breeding and birth data in a population of R. bieti at Mt. Lasha in Yunling Nature Reserve, Yunnan, China, from January 2008 to May 2010, using a combination of 10-min instantaneous scans and ad libitum observations. We examined variations in temperature, rainfall, and food availability, as well as photoperiod differences between Mt. Lasha and the more northerly Xiaochangdu to identify environmental influences on the timing of reproductive events. Our data show the area exhibited distinct seasonal fluctuations in rainfall, temperature, and food availability. Mating occurred year-round, but peaked in August, coinciding with the end of the period of highest temperatures and food availability, and during the peak rainfall. Copulation frequency peaked 1 month after corresponding peaks in staple foods, rainfall, and minimum temperatures, and 3-4 months after peaks in high-quality foods. Births were significantly seasonal, with a birth peak from mid-February to early April, and a mean birth date of 14 March. Eleven births occurred in 41 days in 2009, and 16 births occurred in 52 days in 2010. Births occurred during periods of increasing temperatures and food availability. Our findings are suggestive of at least one environmental control of conception timing, and support the notion that food availability during key reproductive stages is an ultimate factor for birth seasonality, but provide no supporting evidence for photoperiod during the conception season as a proximate cue to reproduction in R. bieti.

Copulation patterns are important to understanding male mating strategies and stabilization strategies of social organizations in primates. However, information on copulation patterns of Asian primates is relatively rare. This study was undertaken to collect data on mating behavior and birth seasonality of Black-and-white Snub-nosed monkeys (Rhinopithecus bieti) using all occurrence sampling and Focal animal-scan sampling methods at Mt. Lasha, between January and December, 2011. Our study focused on observing mating frequency and birth rates. Snub-nosed monkeys mate year round, with two observable peaks: one reproductive peak during the mating season, roughly from August to October, and a second non-breeding peak during the birth season. It is unclear what biological significance this non-reproductive mating peak has. During our observation, we noted a lower ratio of mount to ejaculation and rare ejaculatory copulations, which indicated that every mating would not result in ejaculation. This study corroborates the previous view that the Rhinopithecus bieti's copulatory pattern is likely multiple-mount ejaculation (MME) or at the upper part of mating continuum of single-mount ejaculation (SME) toward MME. More ejaculatory copulations initiated by males than females indicate that MME is not only a mating strategy of males, but that males can influence the position of their copulatory pattern on the continuum between SME and MME. The mating frequencies significantly correlated with the birth rates with a delay of 6 to 7 months. Monkeys gave birth within a strict seasonality with a birth peak of March, which confirms the previous view. Infants were born with a certain degree of synchronization, but different populations displayed different modes of synchronizations.