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Nutrient Requirements of Nonhuman Primates: Second Revised Edition (2003)
Board on Agriculture and Natural Resources (BANR)

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Nutrient Requirements of Nonhuman Primates: Second Revised Edition, 2003

Leavesdominate other plant parts

Avahi

A. laniger

Woolly lemur

Seasonally exclusively folivorous: 91% leaves (40% mature leaves, 51% mixed mature and young), 9% flowers, rarely fruit and bark

Nocturnal, arboreal, monogamous pairs, groups 2-5 individuals

1.3 kg female, 1.0 kg male

Albignac, 1981; Ganzhorn, 1988; Ganzhorn et al., 1985; Harcourt, 1991; Kappeler, 1991; Richard & Dewar, 1991

Indri

I. indri

Indri (babakoto)

Young leaves, buds, and petioles 45% (1-75%), fruit 38% (5-75%), unripe seeds 12% (10-15%), flowers and buds 3% (1-6%), mature leaves 2% (0-3%), occasionally soil

Diurnal, arboreal, monogamous family groups 2-6 individuals

7.1 kg female, 5.8 kg male

Hladik, 1979; Mittermeier et al., 1994; Pollock, 1975, 1977

Lepilemur

L. dorsalis

L. edwardsi

L. leucopus

L. microdonc

L. mustelinus

L. ruficaudatus

L. septentrionalis

Gray-backed sportive lemur

Milne-Edwards’ sportive lemur

White-footed sportive lemur

Small-toothed sportive lemur

Weasel sportive lemur

Red-tailed sportive lemur

Northern sportive lemur

Leaves primarily, some fruit, bark, seeds, flowers; L. mustelinus can tolerate high alkaloid levels; L. ruficaudatus may practice caecotrophy and have high tolerance for toxins; L. leucopus 100% leaves

Nocturnal, arboreal, solitary or male/ female pairs, sleep 1-3; do not hibernate

544-915 g, L. edwardsi 1000g

Albignac, 1981; Charles-Dominique & Hladik, 1971; Ganzhorn, 1988; Hladik, 1979; Hladik & Charles-Dominique, 1974; Hladik et al., 1980; Kappeler, 1990, 1991; Kappeler & Ganzhorn, 1993; Nash, 1994; Silva & Downing, 1995

Propithecus

P. diadema

P. tattersalli

P. verreauxi

Diademed sifaka

Golden-crowned sifaka

Verreaux’s sifaka

P. diadema and P. tattersalli: young leaves 25% (5-44%), mature leaves 25% (0-46%), fruit, ripe or unripe 43% (0-72%), flowers 7% (0-23%); P. verreauxi: mature leaves 38% (2-70%), young leaves 40% (0-70%), fruit 7% (5-8%), flowers 10% (0-40%), bark 5% (4-9%)

Diurnal, mostly arboreal, pairs to multimale/ multifemale groups, 2-12 individuals

P. diadema: 5.6-7.2 kg, P. tattersalli: 2.1-3.8 kg, P. verreauxi: 3.5-3.6 kg

Hemingway, 1998; Hladik, 1979; Jolly, 1966; Kappeler, 1991; Meyers & Wright, 1993; Richard, 1974, 1977, 1978; Yamashita, 1996

Mostly bamboo

Hapalemur

H. aureus

H. griseus

H. simus

Golden bamboo lemur

Lesser bamboo lemur

Greater bamboo lemur

Bamboo 95% (85-98%) (shoots 89%, mature leaves 6%, young leaves 1%, petioles 1%), flowers 1%, fruit 2%, fungus 2%; H. griseus also eats phragmites leaves and shoots, Papyrus pith; H. aureus eats a bamboo containing 12 × lethal dose (for humans) of cyanide

Diurnal or cathemeral, arboreal, family 2-6 individuals; H. simus 1 male + multifemale or multimale/ multifemale groups 4-30 individuals

H. aureus 1.5 kg female, 1.7 kg male; H. griseus 800-939 g; H. simus 1.3-2.4 kg

Glander et al., 1989; Kappeler, 1990; Meier & Rumpler, 1987; Overdorff et al., 1997; Petter & Peyrieras, 1970a; Petter et al., 1975, 1977; Silva & Downing, 1995; Wright, 1986; Wright & Randrimanantena, 1989; Wright et al., 1987

Wasthought of asinsectivorousbut isomnivorous-frugivorous

Daubentonia

D. madagascariensis

Aye-aye

Seeds/nuts 47% (12-84%), nectar 8% (1-20%), larvae 20% (2-45%), canker 20% (5-42%), other (soft fruit, fungus, galls, bamboo) 5% (0-12%); larvae extracted with long thin finger; eat coconuts (0-58% where available) same way.

Nocturnal, arboreal, forage solitary, sleep 1-2

2.6 kg female, 2.8 kg male

Ancrenaz et al., 1994; Andriamasimanana, 1994; Erickson, 1995; Iwano & Iwakawa, 1985; Kappeler, 1991; Petter & Peyrieras, 1970b; Pollock et al.,1985; Sterling, 1994; Sterling et al., 1993

aDiet format: mean (range).

bBody weights in ranges whenever possible; single numbers are not averages but indicate that only one individual of the species has been weighed in the wild.

cNo data available from the wild but assumed to be similar to congenerics.

often 1 day. Usually combined with focal-animal sampling, this is an excellent but difficult method for recording foraging and feeding behavior. Start-and-stop rules, independent of the behavior being studied, are required.

  • Sequence Sampling. A sampling period starts with the beginning of a sequence of a chain of behaviors, such as foraging for insects and feeding. The sampling period ends when the observed sequence ends. This method is of lim-

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