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Percentage composition of the annual diets of Presbytis rneluphos (Pm) and P. rubicundu (Pr) 41 Plant part ": , of diet of Pm yn of diet of Pr ~.

Percentage composition of the annual diets of Presbytis rneluphos (Pm) and P. rubicundu (Pr) 41 Plant part ": , of diet of Pm yn of diet of Pr ~.

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The diets of the banded leaf monkey (Presbytis melalophos) at Kuala Lompat in the Krau Game Reserve of West Malaysia and the red leaf monkey (Presbytis rubicunda) in Sepilok Virgin Jungle Reserve, Sabah, East Malaysia have been examined in relation to plant chemistry. Both monkeys spent about half their time eating foliage, and about half their tim...

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... annual diet of both monkeys is similar in terms of plant parts ( Table 4) they ate. The items most highly favoured by both colobines are seeds and, to a lesser extent, young leaves. ...

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... Having a multiple-chambered stomach, the proboscis monkey possesses unique digestive physiology that allows the anaerobic cellulolytic bacteria in their forestomach to ferment their food, and they are capable of regurgitating like the ruminants [16,18]. Nevertheless, sugar-rich fruits are avoided as the fermentation process will increase acidity in their forestomach and cause bloating that could be fatal to them [14,19,20]. In addition, tree bark, termites and termite nest materials are also consumed, though infrequently, by the proboscis monkey for supplement mineral intake, used as a buffer to forestomach pH and removal of toxicity [14]. ...
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    ... However, contrary to earlier assumptions that colobines are almost exclusively folivores, considerable variation in their diet has been reported (Fashing 2011;Kirkpatrick 2011). Indeed, a higher reliance on fruits and/or seeds as food during periods of high fruit availability has been reported in various Asian colobines, e.g., Presbytis percura (Megantara 1989); P. melalophos (Davies et al. 1988); P. potenziani (Hadi et al. 2011); P. rubicunda (Davies 1991;Ehlers Smith et al. 2013;Hanya and Bernard 2012); P. thomasi (Gurmaya 1986); Trachypithecus obscurus (Ruslin et al. 2019); Semnopithecus vetulus (Dela 2007;Hladik 1977); Pygathrix nemaeus (Phiapalath et al. 2011;Ulibarri 2013); Rhinopithecus roxellana (Guo et al. 2007;Yiming 2006;Zhao et al. 2015) and Nasalis larvatus (Matsuda et al. 2009;Yeager 1989). Remarkably, colobines living in human-modified habitats like forests with a mosaic of village gardens and rubber plantations (Dela 2011) or urban and agro-forested areas and forest fragments (Ruslin et al. 2019) tend to consume more fruits than reported in more natural habitats. ...
    ... The study group inhabiting the human-modified forest patch consumed 29 species from 18 plant families, fewer than a conspecific inhabiting a speciesrich rainforest patch in Singapore (53 species from 33 families), though it was evaluated not only by the direct observation but also metagenomic shotgun sequencing of fecal samples (Srivathsan et al. 2016). Comparing our finding to other studies of Asian colobines, the number of plant species consumed by the study group was particularly low (e.g., Presbytis percura: 136 plant species consumed; P. melalophos: 55 species (Davies et al. 1988); P. potenziani: 118 species (Hadi et al. 2011); P. rubicunda: 64-122 species (Davies 1991;Ehlers Smith et al. 2013;Hanya and Bernard 2012); Trachypithecus obscurus: 130 species (Ruslin et al. 2019); Pygathrix nemaeus: 79 species (Ulibarri 2013); Nasalis larvatus: 188 species (Matsuda et al. 2009). Note, however, that it is impossible to directly compare the number of consumed plant species between this study and others because of differences in sampling methods and habitats. ...
    ... The study group predominantly consumed young leaves (51%); in addition, the percentage of fruits consumed (45%) is comparable to fruit consumption in other Asian colobines, e.g., T. obscurus: 40% fruit consumption (Ruslin et al. 2019); Semnopithecus vetulus: 60% (Dela 2007); P. percura: 58% (Megantara 1989); P. melalophos: 50% (Davies et al. 1988); P. potenziani: 55% (Hadi et al. 2011);P. rubicunda: 84% (Ehlers Smith et al. 2013); P. thomasi: 67% (Gurmaya 1986); Nasalis larvatus: 40% (Yeager 1989). ...
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    ... For example, most primates are described as folivores, frugivores, insectivores or some combination of these terms. Among folivores, the distinction is often made between components of young and mature foliage in the diet [1][2][3]. Young leaves are considered a higher quality food having more protein and less fibre, while low-quality mature leaves have the inverse [4]. The amount of fibre is related to the effort needed to process food because it is thought to enhance the property of toughness [5,6], which is considered the most critical variable when discussing the breakdown of leaves into digestible matter [7,8]. ...
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    The material property of leaf toughness is considered the crucial mechanical challenge facing folivorous primates. Mature leaves have higher recorded toughness values than young leaves on average, leading to many assumptions about the patterning of food breakdown that follow a tough/not-tough dichotomy. We tested three hypotheses about how leaves break down under repetitive loading cycles, predicting that mature leaves (i) experience more force during simulated occlusal loads, (ii) more effectively resist fragmentation into small pieces, and (iii) show a more gradual decline in resistance over consecutive cycles than young leaves. Under displacement control using a mechanical testing system, we subjected young and mature leaves to 20 cycles of axial loading using interlocking steel wedges, then collected and quantified the size of the leaf fragments. While we found that mature leaves experienced more overall force than young leaves ( p < 0.001), they also shattered into smaller pieces ( p = 0.004) and showed a steeper decline in their resistance to the cycles over the course of a test ( p < 0.01). These results suggest that putatively ‘tougher’ foods (i.e. mature versus young leaves) do not necessarily resist fragmentation as commonly assumed. The current tough/not-tough paradigm of primate foods may not accurately reflect how leaves break down during masticatory behaviour.