In a world increasingly dominated by human demand for agricultural products, we need to understand wildlife's ability to survive in agricultural environments. We studied the interaction between humans and Javan slow lorises (Nycticebus javanicus) in Cipaganti, Java, Indonesia. After its introduction in 2013, chayote (Sechium edule), a gourd grown on bamboo lattice frames, became an important cash crop. To evaluate people's use of this crop and to measure the effect of this increase on slow loris behaviour, home ranges, and sleep sites, we conducted interviews with local farmers and analysed the above variables in relation to chayote expansion between 2011-2015. Interviews with farmers in 2011, 2013 and 2015 confirm the importance of chayote and of bamboo and slow lorises in their agricultural practises. In 2015 chayote frames covered 12% of land in Cipaganti, occupying 4% of slow loris home ranges, which marginally yet insignificantly increased in size with the increase in chayote. Slow lorises are arboreal and the bamboo frames increased connectivity within their ranges. Of the sleep sites we monitored from 2013-2016, 24 had disappeared, and 201 continued to be used by the slow lorises and processed by local people. The fast growth rate of bamboo, and the recognition of the value of bamboo by farmers, allow persistence of slow loris sleep sites. Overall introduction of chayote did not result in conflict between farmers and slow lorises, and once constructed the chayote bamboo frames proved to be beneficial for slow lorises.
Among primates, the suborder Haplorhini is considered to have evolved a consolidated monophasic sleep pattern, with diurnal species requiring a shorter sleep duration than nocturnal species. Only a few primate species have been systematically studied in their natural habitat where environmental variables, including temperature and light, have a major influence on sleep and activity patterns. Here we report the first sleep study on a nocturnal primate performed in the wild. We fitted seven wild Javan slow lorises ( Nycticebus javanicus ) in West Java, Indonesia with accelerometers that collected activity data, and installed climate loggers in each individual’s home range to collect ambient temperature readings (over 321 days in total). All individuals showed a strictly nocturnal pattern of activity and displayed a striking synchronisation of onset and cessation of activity in relation to sunset and sunrise. The longest consolidated rest episodes were typically clustered near the beginning and towards the end of the light period, and this pattern was inversely related to daily fluctuations of the ambient temperature. The striking relationship between daily activity patterns, light levels and temperature suggests a major role of the environment in shaping the daily architecture of waking and sleep. We concluded that well-known phenotypic variability in daily sleep amount and architecture across species may represent an adaptation to changes in the environment. Our data suggest that the consolidated monophasic sleep patterns shaped by environmental pressures observed in slow lorises represent phylogenetic inertia in the evolution of sleep patterns in humans.
65sleep and sleep site selection, a comparative approach is required (Elgar, Pagel and Harvey, 1988; 66 Lesku, Roth II, Amlaner and Lima, 2006;Rattenborg, Martinez-Gonzalez and Lesku, 2009). Sleep can 67 comprise more than 50% of a primate's activity budget (Campbell and Tobler, 1984 79that are self-constructed or constructed by other species. Use of nests (either self-constructed or made in 80 tree holes or hollows) and platforms as sleep sites is common among strepsirhines and great apes, and, 81 presumably, the earliest humans (Sabater, Veá and Serrallonga, 1997;Bearder et al., 2003; Fultz, Brent, 82 Breaux and Grand, 2013;Samson and Shumaker, 2015b), but are rarely used by other haplorhines. 83Samson and Nunn (2015) distinguished these assembled nests, on the basis that for larger primates, tree 84 hollows would not be a viable sleeping option, and suggest that ancestral Paleocene and Eocene 85primates probably had galago-like fixed point nest use. Since most monkeys do not use nests, nest use 86 must have evolved multiple times. To be able to infer potential sleep site patterns in early primates (i.e. 87the ones for which only morphological data are available), we also must examine how body size, forelimb 88 to hindlimb ratio, and hand dexterity combine to assist living primates in their sleep site choices (Covert, 89 2002; Gebo and Dagosto, 2004). 4To examine the question further, Kappeler (1998) Rasmussen (1986) and Ehrlich and MacBride, (1989)]. 98Regarding the paucity of field data on many primate taxa, he urged further research of wild primates to 99 understand better the evolution of sleep site selection. 105In the twenty-first century, substantial taxonomic changes have occurred for both the African and Asian 106 lorisiforms. First, the dwarf galagos of the genus Galagoides were recognized as a polyphyletic clade 107 (Pozzi et al., 2015), and now are comprised of Galagoides (western and central Africa) and Paragalago 108(eastern Africa). Paragalago is a sister taxon to the genus Galago, and Galagoides and is a sister taxon 109 to the clade containing Sciurocheirus, Otolemur, Paragalago and Galago (Masters et al., 2017 132These data can be used as a basis to understanding ancestral sleep behavior of primates that can help to 133 inform sleep patterns that occurred later in primate evolution. 135 MATERIAL AND METHODS 136We follow the taxonomy of Nekaris 174To gain insight into sleep patterns and the presence of fragmented sleep in the lorisiforms, we compiled 175 data on when individuals entered and exited sleep sites. From selected sites, we added information on 176 pre-or post-dusk waking and pre-or post-dawn sleeping. We added observations of sleep during the 177 night or non-sleep behavior during the day. 178We examined evidence of predation on lorisiforms and highlight those instances where the events 179 occurred while the animal was asleep, or where we could reasonably infer that predation had taken place 180 during the daytime. We excluded predation events by nocturnal p...
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