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Fig. 3 in Proboscis Monkeys (Nasalis Larvatus (Wurmb, 1787)) Have Unusually High-Pitched Vocalizations

Fig. 3. Cumulative curve of mean frequencies of calls in the study. Graph omits the one call that has a frequency <2.7 kHz.

Fig. 2. A in Proboscis Monkeys (Nasalis Larvatus (Wurmb, 1787)) Have Unusually High-Pitched Vocalizations

Fig. 2. A sample spectrogram of a high frequency vocalization of the proboscis monkey, Nasalis larvatus, that shows the harmonic structure of these calls. The fundamental frequency of this call ranges from 3.4–5.4 kHz and the mean frequency is 4.9 kHz.

Fig. 3 in Nasalis larvatus (Primates: Colobini)

Fig. 3.—Nasalis larvatus is endemic to the island of Borneo in Brunei, the Malaysian states of Sarawak and Sabah and the Indonesian states of Daerah Tingkat I Kalimantan Barat, Kalimantan Tengah, Kalimantan Selatan, and Kalimantan Timur, collectively shown as Kalimantan. Some place names mentioned in the text are shown. Based on Meijaard and Nijman (2000a) and Sha et al. (2008).

Fig. 2 in Nasalis larvatus (Primates: Colobini)

Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male Nasalis larvatus. Occipitonasal length is 133 mm. Photographed by Phil Myers, Museum of Zoology, University of Michigan; used with permission of the photographer. First published by http://animaldiversity.org.

Fig. 3 in Co-infection patterns of intestinal parasites in arboreal primates (proboscis monkeys, Nasalis larvatus) in Borneo

Fig. 3. Differences in width among trichurid egg morphotypes found in proboscis monkey feces. (T1 n = 11, T2 n = 30, T3 n = 30, T4 n = 2, and T5 n = 10). Median, boxes define the 25th and 75th percentiles, whiskers extend to maximum ± 1.5 times the interquartile range (IQR = middle 50% of the records). *p = 0.05; **p = 0.001; ***p = 0.0001.

Fig. 2 in Co-infection patterns of intestinal parasites in arboreal primates (proboscis monkeys, Nasalis larvatus) in Borneo

Fig. 2. Taxonomic diversity of helminth parasites found in proboscis monkeys. The five detected helminth orders were: the order Enoplida, trichurids (morphotypes T1-T4 genus Trichuris, T5 genus Anatrichosoma), the order Strongylida (morphotypes S1 genus Trichostrongylus, S2 genus Oesophagostomum/Ternidens, S3 unknown strongylid), the order Rhabditida, genus Strongyloides (R), the order Ascaridida, genus Ascaris (with exfoliated rough brown outer shell layer) (A) and the order Oxyurida, genus Enterobius (O). Scale bars = 50 Mm. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article).

Fig. 1 in Co-infection patterns of intestinal parasites in arboreal primates (proboscis monkeys, Nasalis larvatus) in Borneo

Fig. 1. Sample collection sites along the Kinabatangan River in Borneo. The island of Borneo, South-East Asia, with position of Lot 6 on the southern riverbank in the Lower Kinabatangan Wildlife Sanctuary in Sabah, Malaysian Borneo. Map reproduced according to GPS data points collected and mapped via Garmin Map Source (version 6.16.3).

Fig. 4 in Co-infection patterns of intestinal parasites in arboreal primates (proboscis monkeys, Nasalis larvatus) in Borneo

Fig. 4. Differences in length among strongylid egg morphotypes found in proboscis monkey feces. (S1 n = 30, S2 n = 30, and S3 n = 17). Median, boxes define the 25th and 75th percentiles, whiskers extend to maximum ± 1.5 times the interquartile range (IQR = middle 50% of the records). *p = 0.05; **p = 0.001; ***p = 0.0001.

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Fig. 3. Land use and land cover data for 2014 in Population trends and conservation status of proboscis monkeys (Nasalis larvatus) in the face of habitat change in the Klias Peninsula, Sabah, Borneo, Malaysia

Fig. 3. Land use and land cover data for 2014/2015 within the 1-km buffer distance from surveyed rivers, overlaid with proboscis monkey sightings from the 2004/2005 and 2014 surveys, Protected Areas, and Production Forest Reserve boundaries.

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Fig. 2 in Population trends and conservation status of proboscis monkeys (Nasalis larvatus) in the face of habitat change in the Klias Peninsula, Sabah, Borneo, Malaysia

Fig. 2. Boxplots illustrating the variation in vegetation variables, with each point representing the values for vegetation plot in each site.

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Fig. 1 in Population trends and conservation status of proboscis monkeys (Nasalis larvatus) in the face of habitat change in the Klias Peninsula, Sabah, Borneo, Malaysia

Fig. 1. Map showing the Klias Peninsula region in western Sabah, in the northern part of Borneo (inset), Malaysia, and the research sampling sites in riverine, mangrove, and mixed mangrove-riverine forests along rivers in Padang Teratak Bird Sanctuary, Padas Damit Forest Reserve, Menumbok Forest Reserve, Binsulok Forest Reserve, Klias Forest Reserve, Kg. Hindian Forest Reserve, and Nabahan Forest Reserve, where the river surveys of the sleeping sites of proboscis monkeys were conducted.

Fig. 1. A in Proboscis Monkeys (Nasalis Larvatus (Wurmb, 1787)) Have Unusually High-Pitched Vocalizations

Fig. 1. A male proboscis monkey in the Singapore Zoological Gardens.

Fig. S1 in Proboscis Monkeys (Nasalis Larvatus (Wurmb, 1787)) Have Unusually High-Pitched Vocalizations

Fig. S1. Spectrogram of Call 2: Low frequency vocalization produced by adult male.

Fig. 4 in Nasalis larvatus (Primates: Colobini)

Fig. 4.—Leaping style of Nasalis larvatus. Photograph by Lee Harding.

Fig. 5 in Nasalis larvatus (Primates: Colobini)

Fig. 5.—Nasalis larvatus juvenile showing single-arm suspensory feeding. Photograph by Lee Harding.

Fig. 1 in Nasalis larvatus (Primates: Colobini)

Fig. 1.—Nasalis larvatus female (above) and male (below). Photographs by Lee Harding.