List of herbivorous animals explained
This is a list of herbivorous animals, organized in a roughly taxonomic manner. In general, entries consist of animal species known with good certainty to be overwhelmingly herbivorous, as well as genera and families which contain a preponderance of such species.
Herbivorous animals are heterotrophs, meaning that they consume other organisms for sustenance. The organisms which herbivores consume are primary producers, predominantly plants (including algae). Herbivores which consume land plants may eat any or all of the fruit, leaves, sap, nectar, pollen, flowers, bark, cambium, underground storage organs like roots, tubers, and rhizomes, nuts, seeds, shoots, and other parts of plants; they frequently specialize in one or a few of these parts, though many herbivores also have quite diverse diets.
List criteria
Animal diets are not inflexible, and most animals will stray from their typical diet on occasion; for instance, cattle will eat chicks,[1] and crocodiles will consume fruit.[2] Though it can be hard to determine what is a true aberration, as opposed to being a normal, but minor component of the diet, animals are still regarded as herbivores, carnivores, or otherwise as long as the vast majority of their diet reflects such a categorization.[3] Thus, several of the animals which appear on this list are commonly described as omnivores, but, where consumption of animal matter is marginal, they meet the criteria for inclusion. These cases are elaborated upon within the article.
Where quantifiable data to support such an evaluation exist, this list generally includes animals whose diets are at least ~90% herbivorous, as a simple and arbitrary minimum, though a great many listees are far more herbivorous than this; perhaps the majority are closer to 95%, and a large number are nearly purely herbivorous. However, a small selection of taxa which are not usually this herbivorous also receive mention; typically, this is done when the animal is much more herbivorous than the vast majority of close relatives. For example, the maned wolf receives mention; its diet varies from mostly carnivorous to overwhelmingly frugivorous, being mostly a fairly balanced omnivore overall, but they are still listed because no other living Canid is nearly so herbivorous. Other animals may receive mention if at least some populations of the species regularly consume very plant-heavy diets.
The issue is further complicated by variation based on region, sex, age, season, and other factors, as well as differing techniques for measuring dietary proportions and a lack of data on many species. A number of listed taxa also consume a significant quantity of fungi. On the whole, however, this list consists almost entirely of animals which are known with good certainty to be overwhelmingly herbivorous, with exceptions being noted.
Invertebrates
Insects
Herbivory is of extreme ecological importance and prevalence among insects. Perhaps one third (or 500,000) of all described species are herbivores.[4] Herbivorous insects are by far the most important animal pollinators, and constitute significant prey items for predatory animals, as well as acting as major parasites and predators of plants; parasitic species often induce the formation of galls. Herbivorous insects also form symbioses with numerous plants, animals, and fungi, including complex relationships with various species of ant, and have greatly impacted the evolution of plants.
- Larval mayflies are generally herbivorous; adults have short lifespans and do not eat at all.[5]
- Most members of the order Orthoptera; for instance, most grasshoppers and katydids are herbivores[6]
- Butterflies
- Many beetles of the Scarabaeoidea, including many scarabs, like the goliath and rhinoceros beetles (e.g., the hercules beetle), and all of the stag beetles
- The jewel beetles (family Buprestidae)[7]
- Certain ladybugs (family Coccinellidae): The subfamily Epilachninae, comprising 1/6 of all ladybug species, is entirely herbivorous, including members such as the Mexican bean beetle and the bryony ladybird.[8]
- The leaf beetles (family Chrysomelidae)[9]
- The weevils (family Curculionidae)[10]
- Almost all adult bees (clade Anthophila), including mason bees, honeybees, bumblebees, sweat bees, and carpenter bees
- All true bugs (order Hemiptera) outside of Heteroptera are herbivores, including cicadas, leafhoppers, treehoppers, planthoppers, aphids, scale insects, and whiteflies[11]
- Most Heteropterans are also herbivorous,[12] including most of the leaf-footed bugs,[13] seed bugs and their relatives,[14] plant bugs,[15] and shield, stink, and burrowing bugs and their relatives[16]
Other invertebrates
Fish
Herbivorous fish play a key role in maintaining healthy ecosystems, especially in tropical reefs, where they promote a balance between corals and macroalgae.[17] Herbivorous fish include:
- Acanthurus lineatus or lined surgeonfish (also known as blue-banded surgeonfish, blue-lined surgeonfish, clown surgeonfish, pajama tang, striped surgeonfish, and zebra surgeonfish)
- Acanthurus nigrofuscus, known as the lavender tang, brown tang, or spot-cheeked surgeonfish
- Zebrasoma scopas, known as the brown tang, two-tone tang, scopas tang or brush-tail tang.
- The unicornfishes (Nasinae) genus is primarily herbivorous.
- Most of the nearly 100 species of the parrotfish family are herbivores.[18] [19]
- Grass carp, so named for its diet of aquatic plants.
- The various genera of pacu are mostly herbivorous.
- The majority of Loricariidae, including most pleco and Otocinclus species, are predominantly or exclusively herbivorous.
Amphibians
Unusually for tetrapods, herbivory is rare among extant adult lissamphibians. There are, however, many larval and a few adult amphibians which take significant plant matter:
Reptiles
Squamates (lizards, snakes, and worm lizards)
All snakes and the majority of non-snake squamates (lizards) are carnivorous. However, some degree of herbivory is relatively common among lizards. Perhaps 12% of lizards have diets which are >10% herbivorous. Dedicated herbivory, with plants constituting >90% of the diet, occurs in perhaps ~1% of lizards, though estimates vary.[23]
- Iguanas (family Iguanidae) are overwhelmingly herbivores; members such as the rhinoceros iguana, marine iguana, green iguana, Lesser Antillean iguana, chuckwallas, desert iguana, and Galápagos land iguana are virtually exclusively herbivorous
- Members of the family Liolaemidae are herbivores
- The Panay, Northern Sierra Madre forest, and Gray's monitor lizards are the only three species of herbivorous Varanid
- Species of the Agamid genus Uromastyx, the spiny-tailed lizards, are herbivores
- Certain skinks; the Solomon Islands skink is exclusively herbivorous. King's skink is also primarily a herbivore.[24] The extinct Cape Verde giant skink was herbivorous.
Chelonians (turtles/tortoises)
- Tortoises, consisting of the family Testudinidae, are all almost exclusively herbivorous
- Adult green sea turtles are herbivorous, uniquely among sea turtles
Dinosaurs (non-avian)
Birds
Although, by some counts, only 2-3% of extant bird species are primarily herbivorous,[26] herbivorous birds are nonetheless incredibly diverse, having evolved independently within at least nine distinct lineages. Herbivorous birds include important pollinators and seed dispersers, as well as both the smallest and largest living birds (the bee hummingbird and the common ostrich, respectively). On islands with little to no mammalian colonization, large herbivorous birds frequently evolved to assume niches typically held by mammals, sometimes attaining enormous sizes; on the Hawaiian Islands, New Zealand, Madagascar, Mauritius, New Caledonia, and Fiji, birds were nearly if not the largest terrestrial herbivores, though the vast majority are now extinct. Birds which are mostly herbivorous as adults will frequently feed their young a far more insectivorous diet, though there are many exceptions.[27]
Paleognathes
- Ratites, excluding the kiwis, are often described as omnivorous, and will eat varying quantities of small animals and insects. However, the typical wild diet for non-kiwi ratites is overwhelmingly and sometimes exclusively herbivorous:[28]
- Ostrich diets can be over 99% herbivorous,[29] though this may vary, but not significantly[30]
- Rheas: the lesser rhea[31] [32] and greater rhea[33] [34] are essentially 100% herbivorous (though this can drop to 97% for greater rheas in some cases)
- Emus may be nearly 100% herbivorous in wild habitats, but can also engage in significant insectivory at times[35] [36]
- The three species of cassowary are virtually exclusively frugivorous, though the dwarf cassowary's diet can be up to 3% insect at times; cassowaries will also consume significant volumes of mushrooms[37] [38] [39]
- The (recently extinct) moas[40] (order Dinornithiformes) and elephant birds[41] [42] (order Aepyornithiformes) were herbivores
- Tinamous: although data are scarce, many tinamous are quite omnivorous, and some are primarily insectivores.[43] However, the vast majority of tinamous are primarily herbivorous,[44] sometimes nearly exclusively:
Galloanserae
the ducks and their relatives are predominantly herbivorous;[50] although a few species consume primarily animal matter and several are heavily omnivorous, at least a quarter of the 99 species included in one study were 70% herbivorous or more. Herbivorous taxa are varied, including:
- The screamers, such as the southern screamer[51] and the horned screamer,[52] are totally herbivorous
- Magpie geese are essentially purely herbivorous[53]
- The majority of Anatids range from largely to almost exclusively herbivorous (notably excluding the Mergini):
- Whistling ducks are all nearly 100% herbivorous, including the fulvous, white-faced, and black-bellied whistling ducks[54] [55] [56] [57]
- Almost all of the Anserinae, including both young and adults:
- Cape Barren geese are strict herbivores
- Swans (genus Cygnus) are all 100% herbivorous or very nearly so, including the mute,[58] black,[59] black-necked,[60] [61] tundra,[62] [63] trumpeter,[64] and whooper swans
- Black geese (genus Branta) are all exclusively herbivorous; examples include the Canada goose,[65] [66] brant,[67] [68] barnacle goose,[69] [70] and nene[71]
- True geese (genus Anser) are all essentially pure herbivores, such as the greylag,[72] [73] snow,[74] [75] bar-headed, pink-footed,[76] and swan geese[77]
- Certain Tadornines are virtually purely herbivorous (note that the circumscription of Tadorninae varies):
- Australian wood duck diets are >99% herbivorous[85] [86]
- The southern, red-crested, and rosy-billed pochard[87] are all almost exclusively herbivorous[88]
- The Brazilian teal is seasonally 83-98% herbivorous,[89] or ~93% overall
- The masked duck is heavily herbivorous, but its diet is poorly known[90]
- Certain Mareca species are seemingly nearly wholly herbivorous, such as the wigeons[91] [92] [93] [94]
- The four species of moa-nalo were herbivorous; they were large, flightless Anatids native to Hawaii and became extinct in historic times[95]
- Many other Anatid species have diets which vary seasonally; near-exclusive herbivory or carnivory are both possible at different times of year. Many are predominantly herbivorous overall, but they are not typically as herbivorous as most of the taxa listed above
- Galliformes, or the landfowl, are virtually all predominantly herbivorous,[96] [97] including:
- Although the diets of megapodes are very poorly known,[98] at least some species are quite herbivorous; the malleefowl's diet may range from 93-99% plants[99] [100]
- The cracids are nearly all highly frugivorous herbivores;[101] [102] the typical guans, piping guans, chachalacas, black guan, highland guan, horned guan, great curassow, and black curassow all have diets which typically contain <10% animal matter, and frequently almost none[103] [104]
- Many New World quails; the mountain quail's annual diet is 95-97% herbivorous,[105] [106] while the California quail is almost entirely herbivorous year-round,[107] [108] and Gambel's quail is ~95% herbivorous annually (though this can drop to 85% in summer).[109] Juveniles also tend to be exceptionally herbivorous
- A very large selection of Phasianids (though at least some insectivory is typical, especially seasonally and among females):
- Snow partridges and blood pheasants[110]
- All of the tragopans;[111] the satyr tragopan's diet is ~93% herbivorous during the post-monsoon, and otherwise nearly exclusively herbivorous;[112] Temminck's tragopan is overwhelmingly herbivorous year-round[113]
- The monal-partridges[114] [115]
- Monals[116]
- The turkeys:
- Wild turkeys are overwhelmingly herbivorous; although a few studies on annual dietary composition yield values of around 85% herbivorous, most find values at least somewhat above 90%, and values close to 100% are also common[117] [118] [119] [120]
- Ocellated turkeys are nearly 100% herbivorous[121] [122]
- Most grouse are highly herbivorous:[123]
- The ruffed grouse has an annual diet that is ~99% herbivorous, with minor seasonal insectivory[124] [125]
- Male Chinese grouse are purely herbivorous and females are >90% herbivorous;[126] hazel grouse males are purely herbivorous, but some females will consume large quantities of insects in spring (although others are nearly purely herbivorous as well);[127] both are herbivorous in winter[128]
- The sage grouse can be ~90% herbivorous in summer and around 97% herbivorous overall[129] [130]
- The blue grouse: dusky grouse are 98% herbivorous overall and a little less than 90% at lowest, in summer,[131] [132] while sooty grouse are 98-100% herbivorous year-round
- Sharp-tailed grouse are 96% herbivorous in spring and summer,[133] and most studies find them to be nearly wholly herbivorous in fall,[134] although grasshoppers can account for 1/3 of the diet in some cases;[135] they are by far the most herbivorous member of their genus
- All three species of ptarmigan are almost exclusively herbivorous year-round; though they will take insects opportunistically, they are not a major component of the overall diet, even seasonally[136] [137] [138]
- Spruce grouse are >99% herbivorous year-round;[139] [140] Siberian grouse are ~98% herbivorous but may eat some insects seasonally
- Western capercaillies are virtually exclusively herbivorous[141] [142]
- Caucasian and black grouse are 98% herbivorous or more[143] [144] [145]
- Many of the true pheasants:
- The peafowls can be quite omnivorous, and their diets are poorly studied; however, one study finds Indian peafowl diets to be 91% herbivorous overall,[152] and another finds green peafowl diets to be ~96% herbivorous[153]
- The Gallini are largely omnivores which lean moderately to very herbivorous, though a few are predominantly carnivores; their wild diets are poorly studied. Some, however, are known to be overwhelmingly herbivorous; the grey-winged francolin has a diet which is 93% plants[154]
- Several of the Coturnicini are heavily herbivorous:
- The extinct families of Sylviornithidae,[164] Gastornithidae,[165] [166] [167] and Dromornithidae[168] were very likely all herbivores. They were giant, flightless Galloanserae and included genera such as Gastornis, Dromornis, and the relatively recently extinct Genyornis, Sylviornis, and Megavitiornis
Neoaves
- The lesser flamingo[169] [170] and James's flamingo[171] feed nearly exclusively on cyanobacteria and algae (e.g. diatoms); they are the only herbivorous flamingo species and a rare example of terrestrial, filter-feeding herbivores. Their young consume mainly crop milk
- The vast majority of the >300 species of pigeon (order Columbiformes) are almost entirely herbivorous,[172] [173] [174] including young, which consume crop milk along with adult foods. Herbivorous pigeons include:
- Most of tribe Zenaidini:
- Virtually all of tribe Columbini:
- Virtually every species of Patagioenas is close to totally herbivorous, including the white-crowned pigeon,[191] [192] [193] [194] band-tailed pigeon,[195] [196] and red-billed pigeon[197] [198]
- Every species of cuckoo-dove (genera Reinwardtoena, Turacoena, and Macropygia) is essentially completely herbivorous,[199] such as the brown cuckoo-dove[200] [201]
- The collared and turtle doves are overwhelmingly to totally herbivorous,[202] such as the European turtle dove[203] [204] [205] and the Eurasian collared dove[206] [207]
- The rock dove, including the feral pigeon and domestic pigeon, is almost entirely herbivorous in both native and introduced wild habitats,[208] [209] [210] [211] though urban birds will consume human food
- All of the other Columba species are also overwhelmingly to totally herbivorous,[212] such as the speckled pigeon,[213] Nilgiri wood pigeon,[214] silvery pigeon,[215] trocaz pigeon,[216] [217] white-headed pigeon,[218] black wood pigeon,[219] [220] [221] and common wood pigeon[222] [223] [224]
- Spilopelia and Nesoenas species, such as the spotted dove,[225] [226] laughing dove,[227] and Malagasy turtle dove[228]
- American ground doves, such as the blue ground dove[229] and Columbina species such as the Inca dove,[230] [231] common ground dove,[232] [233] scaled dove,[234] and ruddy ground dove; the latter 3 are known to be >99% herbivorous annually
- Most of the Phabini are nearly totally herbivorous (though some are quite insectivorous); the white-throated ground dove,[235] bronzewings like the common bronzewing and flock bronzewing,[236] [237] [238] the crested pigeon,[239] the chestnut-quilled and white-quilled rock pigeons, all of the Geopelia doves, such as the diamond dove and zebra dove,[240] and the spinifex pigeon and partridge pigeon[241] [242] are all typically exclusively herbivorous, or nearly so (>99% where data are available, though occasionally slightly less for certain species)
- The tribe Raphini: the thick-billed ground pigeon,[243] pheasant pigeon,[244] tooth-billed pigeon,[245] [246] nicobar pigeon,[247] and crowned pigeons,[248] such as the Victoria crowned pigeon,[249] are all overwhelmingly herbivorous, though several may consume invertebrates in appreciable amounts
- Most members of tribe Turturini, including the brown doves,[250] [251] [252] the namaqua dove,[253] [254] and most Turtur doves,[250] such as the emerald-spotted wood dove,[255] are either wholly herbivorous or consume marginal quantities of invertebrates
- All of the green pigeons (genus Treron) are virtually exclusively herbivorous,[256] including species such as the pink-necked,[257] orange-breasted,[258] African,[259] Madagascar,[260] and thick-billed green pigeons;[261] they are frugivorous, with minor deviations
- Virtually all of Ptilinopini:
- All of the imperial pigeons (Ducula) are usually 100% herbivorous furgivores;[262] they include species such as the collared,[263] mountain, green, white-bellied, goliath,[264] Marquesan,[265] and Torresian imperial pigeons. Opportunistic insectivory is very rare, but reported at least once
- The fruit doves (Ptilinopus) are also frugivores, and are all close to 100% herbivorous,[266] including the rose-crowned, wompoo, superb, orange-bellied, ornate, beautiful, pink-spotted, coroneted, and black-naped fruit doves.[263] Female orange fruit doves have been observed eating caterpillars, but the species is nearly totally herbivorous overall
- The cloven-feathered dove[267] and the blue pigeons are seemingly totally herbivorous[268]
- The New Zealand pigeon,[269] topknot pigeon,[270] sombre pigeon, Papuan mountain pigeon and their relatives are all virtually totally herbivorous[271]
- All of the recently extinct species of pigeon, such as the dodo,[272] [273] the Rodrigues solitaire,[274] the passenger pigeon,[275] [276] the Viti Levu giant pigeon,[277] and the Choiseul pigeon; though their diets are generally poorly known, they were all predominantly to totally herbivorous
- All 16 species of sandgrouse (order Pterocliformes) are almost exclusively herbivorous, eating primarily small seeds.[278] [279] The pin-tailed sandgrouse and black-bellied sandgrouse may be 98% and 99% herbivorous, respectively,[280] while the Pallas's sandgrouse[281] and Namaqua sandgrouse[282] [283] are both apparently 100% herbivorous. The painted sandgrouse is herbivorous apart from minor, seasonal insect consumption
- Two lineages of Strisores:
- The oilbird (the only species in order Steatornithiformes) has a diet consisting almost entirely of fruit.[284] [285] [286] It is the only herbivorous Strisore apart from the hummingbirds, as well as the only nocturnal, frugivorous flying bird in the world; their young are also frugivores
- Virtually all of the >300 species of hummingbird (family Trochilidae) are overwhelmingly nectarivorous.[287] [288] Insectivory is widespread and nutritionally important, but the typical diet is probably about 90% nectar and 10% arthropod by mass,[287] [289] with time budget records yielding similar ratios (~5-15% of feeding time devoted to insectivory). Exceptional (including exclusive) and sustained insectivory has been documented, although these accounts have also been met with skepticism.[290] On the opposite extreme, overwhelmingly nectarivorous diets have also been documented for several species:
- Populations of shining sunbeam have been recorded spending 93-97% of total feeding time on nectar[291]
- Purple-throated caribs have had nectar feeding time budgets of >99% recorded[292] (although extremely low figures are also recorded for this species, but they are likely erroneous)
- In fiery-throated hummingbirds, insectivory accounts for a little over 1% of total feeding time in males, and ~8% in breeding females
- Cuckoos (order Cuculiformes) are largely insectivorous or omnivorous. A small number, however, are primarily frugivores,[293] including the Asian koel[294] [295] and the channel-billed cuckoo,[296] though both also consume a small but significant quantity of animal matter. The dwarf koel may be entirely frugivorous.[297] [298] Young of the former two species (which are brood parasites) will eat partially or wholly fruit diets if they are reared by frugivorous species
- All 23 species of turaco (order Musophagiformes) are either exclusively herbivorous or consume very small amounts of invertebrates;[293] they are largely fruit-eaters, though leaves and other plant parts can be important. Fruits and leaves make up 98-100% of the diets of the great blue, Rwenzori, and black-billed turacos;[299] the western plantain-eater[300] and violet turaco[301] are virtually wholly frugivorous
- The bustards (order Otidiformes) are quite omnivorous, and their diets are variable; several consume mostly animal matter, either seasonally or year-round. However, it has been suggested that the majority of bustards are predominantly herbivorous;[302] such species for which data are available include:
- The diet of the great bustard can be as low as 60% or 70% herbivorous seasonally, but is 87.5%, 93%, or nearly 100% herbivorous annually, with some populations consuming 4% animal matter at most[280] [303] [304]
- One study finds the little bustard to be 26% insectivorous in winter and ~40% otherwise; however, other studies find that the winter diet is 100% herbivorous,[305] or that the diet is 97-100% herbivorous year round[306]
- The food part of the karoo korhaan's diet is 86-87% plant matter[307]
- The hoatzin, the sole living member of Opisthocomiformes, is 100% herbivorous;[308] [309] they are largely folivorous, including young, and have unique gastrointestinal adaptations to this diet
- A selection of gruiforms are predominantly herbivorous, including:
- All three of the trumpeters (family Psophiidae) are ~90% frugivorous, with the remainder of their diets consisting of small animals[310] [311]
- Although the cranes (family Gruidae) are omnivorous to varying degrees, most are primarily herbivorous:
- The Siberian crane is predominantly and sometimes exclusively herbivorous,[312] [313] [314] though precise data are scarce
- The sandhill crane's diet varies, but has been found to be 80%,[315] 85%,[316] or over 95%[317] [318] [319] herbivorous across various seasons and locales; much lower figures (~11%) have also been recorded,[320] but are less typical
- Though precise data are lacking, the white-naped crane,[321] [322] brolga,[323] [324] [325] and sarus crane[326] are also heavily herbivorous
- Most (but not all) other cranes are overwhelmingly herbivorous, including the blue crane[327] [328] and wattled crane.[329] The common crane is >90% herbivorous in winter,[330] while the winter diet of black-necked cranes is 86% herbivorous.[331] The demoiselle crane is 80-97% herbivorous during spring and autumn migration[332] [333]
- Although exact data are lacking, the rails (family Rallidae) are mostly omnivores.[334] However, several species lean herbivorous, and a few are overwhelmingly herbivorous:
- Two lineages of Charadriiformes contain a few overwhelmingly herbivorous species:
- The palm-nut vulture is the only primarily herbivorous accipitriform in the world; its diet may be 45-65% herbivorous,[353] [354] [355] and young may be fed diets which are >90% herbivorous. They specialize in the fruits of palms, but will also consume fish and other animal matter. Many other accipitriforms will consume some plant matter,[356] but far less regularly
- All six species of mousebird are almost entirely herbivorous, with insect consumption being rarely documented;[357] they are largely frugivorous, including the white-backed mousebird[358] and speckled mousebird[359]
- All five of the quetzals in genus Pharomachrus are specialized frugivores;[360] [361] species such as the resplendent quetzal[362] [363] are almost entirely herbivorous as adults. Quetzals are the most herbivorous of the trogons, but several other species are also quite herbivorous, especially in genus Trogon
- A large number of hornbill species (family Bucerotidae) are overwhelmingly herbivorous; these species are important seed dispersers and mostly frugivorous, although they will take animals, particularly while rearing young.[364] They include such birds as:
- The black-casqued and yellow-casqued hornbills are overwhelmingly frugivorous;[365] the former has been recorded as 94% herbivorous during nesting season[366]
- All the Bycanistes hornbills: the black-and-white casqued,[367] brown-cheeked, piping, and silvery-cheeked hornbills[368] all have nesting season diets which are 90-94% herbivorous
- Every Rhyticeros hornbill: the Narcondam hornbill and Sumba hornbill have no animal food recorded in their diets (but likely consume a small amount), while the wreathed hornbill is over 95% herbivorous.[369] The red-knobbed hornbill and plain-pouched hornbill both have nesting diets which are 1% insectivorous[370] [371]
- The rufous-necked hornbill is primarily frugivorous, taking small amounts of animal matter,[372] while the Sulawesi hornbill is 85% frugivorous during nesting season.[373] The related Penelopides species are also very herbivorous[374]
- The helmeted hornbill is frugivorous with very minor animal consumption, perhaps ~1% of the diet, even during nesting.[375] [376] However, extended time dedicated to hunting has also been reported
- The hornbills of genus Buceros are extremely herbivorous: the breeding season diet of the rhinoceros hornbill is ~96% herbivorous,[377] whereas that of the great hornbill is 95-99% herbivorous[378] [379]
- The Anthracoceros hornbills are overwhelmingly herbivorous,[380] such as the Malabar pied hornbill.[381] The oriental pied hornbill may be 93% herbivorous during breeding season or nearly totally herbivorous overall
- The Ocyceros hornbills: the non-breeding diet of the Indian grey hornbill is ~92% herbivorous,[382] while the breeding diet of the Malabar grey hornbill is 86% herbivorous[383]
- Ramphastides as a whole is composed largely of herbivores, including birds such as:
- The various birds called barbets, consisting of four closely related families, are generally frugivores with some animal consumption,[384] and include many especially herbivorous species:
- Virtually every species of toucan (family Ramphastidae) is overwhelmingly frugivorous.[394] [397] Toucans are well-documented as taking diverse animal prey items, especially to feed young, but the occurrence of animals in adult diets is likely overemphasized; in one study of 32 species and 326 individual stomachs, only 5.5% contained arthropods, while only 1.2% contained vertebrates. Toucans comprise five genera:
- The green toucanets (genus Aulacorhynchus), such as the emerald toucanet, whose nestling diet is 85-97% herbivorous;[398] in one study, <1% of foraging attempts by adults entailed successful insect capture, most being fed to nestlings[399]
- The aracaris (genus Pteroglossus):[400] 30 total stomachs belonging to red-necked aracari and lettered aracari only contained plants, while the collared aracari and fiery-billed aracari are almost exclusively frugivorous, with only occasional adult consumption of animal matter.[401] The pale-mandibled aracari is only 5.6% insectivorous outside breeding season,[402] and the saffron toucanet is 7% insectivorous year-round[403]
- The dichromatic toucanets (genus Selenidera):[404] 90% of 28 golden-collared toucanet stomachs contained only fruit, while the spot-billed toucanet is 97% herbivorous annually
- The mountain toucans (genus Andigena);[405] the plate-billed mountain toucan is 98% frugivorous, mainly taking insects only for young[406] [407]
- The toucans of genus Ramphastos: the toco toucan is 95% to 97% herbivorous overall,[408] [409] while the channel-billed and red-breasted toucans may be 96% or 100% herbivorous, respectively
- Two genera of Melanerpine woodpeckers contain species which can be exceptionally herbivorous, in certain locations and seasons (but not, generally, overall):
- The genus Melanerpes:[410]
- The sapsuckers (genus Sphyrapicus): the yellow-bellied sapsucker can spend 77% of feeding time on sap in winter,[417] but is 50% herbivorous across the year[418]
- Probably all of the approximately 400 species of parrot (order Psittaciformes) are nearly totally herbivorous,[419] [420] though occasional deviations are observed for some species:
- The New Zealand parrots (Strigopidae):
- The kea is among the most omnivorous of parrots, famously taking invertebrates, small vertebrates, carrion, and even feeding from living sheep.[421] However, the overall diet is exceptionally herbivorous, with estimates ranging from 70% to 95%;[422] [423] during the fruiting season, they may be close to 100% herbivorous[424]
Mammals
Herbivory is quite common among mammals, with herbivores occurring across diverse lineages and in a large variety of sizes, bodyplans, and niches. Both large and small herbivorous mammals are often important prey species for various predators, though the largest, such as the so-called "pachyderms", are generally safe from predation as healthy adults. Large, herbivorous mammals came to dominate global ecosystems in the Cenozoic, and, though vastly reduced in number, they continue to be key features of certain modern ecosystems, such as the Maasai Mara and Kaziranga National Park.
Marsupials
- Most of the extant Diprotodonts, including:
- A relatively small number of Didelphimorphs are primarily herbivorous, such as the woolly opossums
- The recently extinct entire family of pig-footed bandicoots (Chaeropodidae, with one genus, Chaeropus) was probably herbivorous
Placental mammals
Xenarthrans
Afrotheres
Euarchontoglires
- Both species of colugo (Dermoptera) are herbivores
- The great majority of primates:
- The vast majority of lemurs are largely or exclusively herbivorous, including the ring-tailed lemur, the sifakas, the indri, and the bamboo lemurs[428]
- The three species of potto have diets which are ~90% herbivorous[429]
- Slow lorises are majority (and possibly even nearly exclusively) herbivorous, though study findings differ[430]
- Some bushbabies; needle-clawed bushbabies are gum specialists, and the Bioko Allen's bushbaby is primarily frugivorous[429]
- The vast majority of ape and monkey species (the Simiiformes) are wholly or primarily herbivorous,[431] including:
- The majority of the New World monkeys (though several taxa consume insects, some as a primary food source); predominantly or wholly herbivorous New World monkeys include the spider monkeys, muriquis, woolly monkeys, howler monkeys, sakis, and uakaris,[432] among others
- Virtually all Old World monkeys (sensu stricto, excluding apes)[433]
- Vervet monkeys[434] [435]
- Several macaques are overwhelmingly herbivorous, such as the Tibetan,[436] Japanese, Barbary,[437] and Assam macaques[438]
- Although baboons are famously regarded as omnivores and will occasionally consume animals, studies consistently find species, including the yellow,[439] olive,[440] chacma,[441] and hamadryas baboons,[442] to have diets which are ~99% herbivorous
- Mandrill[443] and drill[444] diets are both >95% herbivorous
- Geladas[445]
- All of the Colobines are (or are nearly) purely herbivorous,[446] including the black-and-white colobuses, gray langurs, snub-nosed monkeys, and the proboscis monkey
- All wild apes:
- Gibbon (family Hylobatidae) diets are ~90% herbivorous, on average[447]
- Orangutan diets are typically close to 99% herbivorous, but can range down to 90%, depending on various factors[448] [449]
- The two species of gorilla: western gorillas are ~95% herbivorous overall, while mountain gorillas are closer to 100%[450]
- The two species of chimpanzee (genus Pan):
- Although chimpanzees are well-known for both their insectivory and their hunting, and though diet varies according to several factors, most studies find their diets to be at least ~95% herbivorous and typically more, up to nearly 100%,[451] [452] [453] [454] though a few populations may consume up to >10% animal matter
- Bonobos are perhaps even more herbivorous, though they will consume small amounts of animal matter[455]
- Humans are typically omnivorous, but certain populations are herbivorous or nearly so. These include members of ideological or health movements such as veganism and vegetarianism, cultural or religious traditions such as Rastafari and many sects of the Dharmic faiths, and certain traditional tribal populations, such as the Tarahumara[456]
- A large majority of rodents (Rodentia) are overwhelmingly or exclusively herbivorous,[457] including:
- Naked mole rats[458] and mole-rats[459]
- Old World porcupines (family Hystricidae), such as the Cape porcupine[460]
- New World porcupines (family Erethizontidae) are almost all pure herbivores,[461] such as the North American and Brazilian porcupines
- Chinchillas and viscachas (family Chinchillidae)[462]
- Pacaranas[463] and extinct relatives, such as the giant rodent Josephoartigasia
- Cavies (family Caviidae),[464] such as the guinea pigs, maras, and capybaras
- Agoutis and acouchis[465]
- Pacas[466]
- Degus[467]
- Most Echimyids,[468] including the nutria, hutias, and Atlantic bamboo rat[469]
- Springhares[470]
- The large majority of Sciuromorphs, including:
- Mountain beavers[471]
- Ground squirrels (excluding chipmunks), such as the marmots (e.g., the groundhog), prairie dogs,[472] and golden-mantled ground squirrel[473]
- Chipmunks, though somewhat omnivorous, are still predominantly and often nearly exclusively herbivorous/mycophagous, including the eastern[474] and least chipmunks (though some chipmunks may eat significant quantities of invertebrates, depending on season, age, and sex)
- Sciurus squirrel species, such as the eastern gray and Eurasian red squirrels, are famously somewhat omnivorous, but in their native habitats, their diets are close to 100% herbivorous[475]
- Flying squirrels, such as the northern,[476] red giant,[477] and Japanese dwarf flying squirrels[478]
- Most Sciurids in general,[479] such as the Indian giant, Prevost's,[480] and Indian palm squirrels[481]
- Most Castorimorphs:
- All Lagomorphs;[486] rabbits, hares, and pikas
Laurasiatheres
- A significant number of bats (order Chiroptera) are frugivorous/nectarivorous:
- Herbivory among the Carnivora is quite rare; nonetheless, it occurs among diverse taxa:
- Maned wolves are omnivores whose diet is typically nearly equally split between animals and plants. However, fruits can account for 60% or more of total consumed biomass in some cases (though animals predominate in other cases), making them among the most herbivorous of living Canids[494] [495]
- A few bears:
- A few raccoon relatives (family Procyonidae): kinkajous[507] and olingos[508] are both almost entirely herbivorous
- Red pandas are essentially purely herbivorous[509]
- African palm civets are ~80% herbivorous[510]
- Many Viverrids are omnivorous, and a few are primarily herbivorous:
- All odd-toed ungulates (order Perissodactyla), including:
- All the non-whale even-toed ungulates (order Artiodactyla), including:
- Ruminants, such as deer,[513] Bovids,[514] the pronghorn,[515] musk deers,[516] the giraffes and okapi,[517] and chevrotains (though this last group includes some members that consume a degree of animal matter)[518]
- Many Suina will consume small amounts of animal matter, but they are overwhelmingly herbivorous overall:
- Wild boars, though popularly regarded as omnivores, are always predominantly herbivorous; typically over 90% of the diet is plant matter. In extreme cases, 1/3 of the diet may be animal matter, but in the native range, plants constitute 85% of the diet as a bare minimum, and very often much more, up to nearly 100%[519] [520] [521]
- Other Sus species, such as the Bornean bearded pig[522]
- Babirusas are predominantly herbivorous[523] [524]
- Bushpigs and red river hogs are predominantly herbivorous
- Giant forest hogs are overwhelmingly herbivorous[525]
- Warthogs are virtually purely herbivorous[526]
- The three peccary species are nearly totally herbivorous[527]
- Camelids,[528] such as the dromedary, wild Bactrian, and Bactrian camels, the llama and alpaca, and the guanaco and vicuña
- Hippos will occasionally consume carrion, but are essentially purely herbivorous overall[529] [530]
See also
Notes and References
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- http://www.arkive.org/tibetan-macaque/macaca-thibetana/#text=Threats Tibetan macaque videos, photos and facts – Macaca thibetana
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- Huang . Zhonghao . Huang . Chengming . 17 September 2014 . Dietary adaptations of Assamese macaques (Macaca assamensis) in limestone forests in Southwest China . American Journal of Primatology . 77 . 2 . 171–185 . 10.1002/ajp.22320 . 25231871 . 26144812 . 9 July 2023.
- Post . David G. . December 1982 . Feeding behavior of yellow baboons (Papio cynocephalusin) the Amboseli National Park, Kenya . International Journal of Primatology . 3 . 4 . 403–430 . 10.1007/BF02693741 . 7510879 . 9 July 2023.
- Swedell . Larissa . Johnson . Caley A. . 9 December 2011 . Feeding ecology of olive baboons (Papio anubis) in Kibale National Park, Uganda: preliminary results on diet and food selection . African Journal of Ecology . 50 . 3 . 367–370 . 10.1111/j.1365-2028.2011.01316.x . 9 July 2023.
- Tew . Eleanor . Landman . Marietjie . 17 April 2018 . The contribution of the chacma baboonto seed dispersal in the eastern Karoo,South Africa . African Journal of Wildlife Research . 48 . 2 . 3 . 10.3957/056.048.023002 . 91069352 . 9 July 2023.
- Swedell . Larissa . Schreier . Amy . 8 February 2008 . Composition and Seasonality of Diet in Wild Hamadryas Baboons: Preliminary Findings from Filoha . Folia Primatologica . 79 . 6 . 476–490 . 10.1159/000164431 . 18931503 . 28739928 . 9 July 2023.
- Tutin, C. E.. Ham, R. M.. White, L. J.. Harrison, M. J.. 9108968. The primate community of the Lopé Reserve, Gabon: diets, responses to fruit scarcity, and effects on biomass. 1997. 42. 1. 1–24. 10.1002/(SICI)1098-2345(1997)42:1<1::AID-AJP1>3.0.CO;2-0. American Journal of Primatology. 37902903.
- Owens . Jacob R. . Honarvar . Shaya . 16 September 2015 . From frugivore to folivore: Altitudinal variations in the diet and feeding ecology of the Bioko Island drill (Mandrillus leucophaeus poensis) . American Journal of Primatology . 77 . 12 . 1270 . 10.1002/ajp.22479 . 26375479 . 40650260 . 9 July 2023.
- Web site: Gelada . www.britannica.com . Britannica . 9 July 2023.
- Web site: Primate - Diet . www.britannica.com . Britannica . 9 July 2023.
- Book: Elder . Alice A. . The Gibbons . Hylobatid Diets Revisited: The Importance of Body Mass, Fruit Availability, and Interspecific Competition . 1 January 2009 . https://link.springer.com/chapter/10.1007/978-0-387-88604-6_8 . 133–159 . 10.1007/978-0-387-88604-6_8 . 978-0-387-88603-9 . 9 July 2023.
- Wich . S. A. . 6 December 2006 . Dietary and Energetic Responses of Pongo abelii to Fruit Availability Fluctuations . International Journal of Primatology . 27 . 6 . 1544 . 10.1007/s10764-006-9093-5 . 34096414 . 9 July 2023.
- Knott . Cheryl D. . December 1998 . Changes in Orangutan Caloric Intake, Energy Balance, and Ketones in Response to Fluctuating Fruit Availability . International Journal of Primatology . 19 . 6 . 1069 . 10.1023/A:1020330404983 . 23153018 . 9 July 2023.
- Lodwick . Jessica L. . Salmi . Roberta . 28 August 2019 . Nutritional composition of the diet of the western gorilla (Gorilla gorilla): Interspecific variation in diet quality . American Journal of Primatology . 81 . 9 . 8 . 10.1002/ajp.23044 . 31463957 . 201667142 . 9 July 2023.
- Watts . David P. . Potts . Kevin B. . 22 November 2011 . Diet of chimpanzees (Pan troglodytes schweinfurthii) at Ngogo, Kibale National Park, Uganda, 1. diet composition and diversity . American Journal of Primatology . 74 . 2 . 122 . 10.1002/ajp.21016 . 22109938 . 2027.42/90275 . 15816155 . 10 July 2023. free .
- Book: Goné Bi . Zoro . Wittig . Roman . 25 November 2019 . Long-term diet of the chimpanzees (Pan troglodytes verus) in Taï National Park: interannual variations in consumption . Long-term diet of the chimpanzees (Pan troglodytes verus) in Taï National Park: Interannual variations in consumption . https://www.cambridge.org/core/books/abs/chimpanzees-of-the-tai-forest/longterm-diet-of-the-chimpanzees-pan-troglodytes-verus-in-tai-national-park-interannual-variations-in-consumption/649D55C604337B2AF6889E557305F2F2 . 245 . Cambridge University Press . 10.1017/9781108674218.016 . 9781108674218 . 213447075 . 10 July 2023.
- Gerstner . Katie F. . Pruetz . Jill D. . 30 November 2022 . Wild Chimpanzee Welfare: A Focus on Nutrition, Foraging and Health to Inform Great Ape Welfare in the Wild and in Captivity . Animals . 12 . 23 . 3370 . 10.3390/ani12233370 . 36496890 . 9735707 . free .
- Hamad . Ibrahim . Delaporte . Eric . Raoult . Didier . Bittar . Fadi . Detection of Termites and Other Insects Consumed by African Great Apes using Molecular Fecal Analysis . Scientific Reports . 4 . 1 . 27 March 2014 . 4478 . 10.1038/srep04478 . 24675424 . 3967517 . 2014NatSR...4E4478H .
- Serckx . Adeline . Kühl . Hjalmar S. . Beudels-Jamar . Roseline C. . Poncin . Pascal . Bastin . Jean-François . Huynen . Marie-Claude . Feeding ecology of bonobos living in forest-savannah mosaics: Diet seasonal variation and importance of fallback foods . American Journal of Primatology . Wiley . 77 . 9 . 13 May 2015 . 10.1002/ajp.22425 . 948–962 . 25974229 . 7159761 .
- Connor . W. E. . Cerqueira . M. T. . Connor . R. W. . Wallace . R. B. . Malinow . M. R. . Casdorph . H. R. . The plasma lipids, lipoproteins, and diet of the Tarahumara Indians of Mexico . The American Journal of Clinical Nutrition . 31 . 7 . 1978 . 10.1093/ajcn/31.7.1131 . 1131–1142 . 665563 . 10 July 2023. free .
- Web site: Introduction to the Rodentia . Waggoner, Ben . 15 August 2000 . University of California Museum of Paleontology . 4 July 2014 . 29 April 2009 . https://web.archive.org/web/20090429075637/http://www.ucmp.berkeley.edu/mammal/rodentia/rodentia.html . live .
- Web site: Naked mole-rat . . nationalzoo.si.edu . 25 April 2016 . 10 July 2023.
- Book: Macdonald, D.. Jarvis, Jennifer U.M.. 1984. The Encyclopedia of Mammals. Facts on File. New York. 708–711. 0-87196-871-1. registration.
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- Book: Macdonald . David W. . The Encyclopedia of Mammals . Oxford University Press . 2006 . 0-19-920608-2 .
- Web site: Chinchillidae . Massiha . R. . 2023 . animaldiversity.org . Animal Diversity Web . 10 July 2023.
- Web site: Dinomys branickii . Nguyen . K. . 2001 . animaldiversity.org . Animal Diversity Web . 10 July 2023.
- Web site: Caviidae . Gorog . T. . Myers . P. . 2000 . animaldiversity.org . Animal Diversity Web . 10 July 2023.
- Web site: Dasyproctidae . Myers . P. . 2000 . animaldiversity.org . Animal Diversity Web . 10 July 2023.
- Web site: Cuniculidae . Myers . P. . 2006 . animaldiversity.org . Animal Diversity Web . 10 July 2023.
- Kenagy . G. J. . Veloso . Claudio . Bozinovic . Francisco . Francisco Bozinovic . 1999-01-01 . Daily Rhythms of Food Intake and Feces Reingestion in the Degu, an Herbivorous Chilean Rodent: Optimizing Digestion through Coprophagy . Physiological and Biochemical Zoology . 72 . 1 . 78–86 . 10.1086/316644 . 9882606 . 32432487.
- Web site: Echimyidae - spiny rats . . nhpbs.org/ . New Hampshire's PBS Station . 10 July 2023 . Most species are herbivores and eat seeds, fruit, nuts, leaves, and other plant parts. Some species may also eat insects..
- Web site: American spiny rat . www.britannica.com . Britannica . 11 July 2023.
- Web site: Pedetes capensis . Jackson . A. . 2000 . animaldiversity.org . Animal Diversity Web . 11 July 2023.
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- Carleton . William M. . Food Habits of Two Sympatric Colorado Sciurids . Journal of Mammalogy . Oxford University Press . 47 . 1 . 1966 . 91–103 . 10.2307/1378073 . 1378073 .
- Wrazen . John A. . Svendsen . Gerald E. . Feeding Ecology of a Population of Eastern Chipmunks (Tamias striatus) in Southeast Ohio . The American Midland Naturalist . University of Notre Dame . 100 . 1 . 1978 . 2424789 . 190–201 . 10.2307/2424789 . 11 July 2023.
- MOLLER . H. . Foods and foraging behaviour of Red (Sciurus vulgaris) and Grey (Sciurus carolinensis) squirrels . Mammal Review . Wiley . 13 . 2–4 . 1983 . 10.1111/j.1365-2907.1983.tb00270.x . 81–98.
- Web site: Glaucomys sabrinus . Malamuth . E. . Mulheisen . M. . 2011 . animaldiversity.org . Animal Diversity Web . 11 July 2023.
- Book: Thorington Jr., R.W. . J.L. Koprowski . M.A. Steele . J.F. Whatton . 2012 . Squirrels of the World . 116–122 . Johns Hopkins University Press . Baltimore . 978-1-4214-0469-1 .
- Web site: Pteromys momonga . Watkins . T. . 2002 . animaldiversity.org . Animal Diversity Web . 11 July 2023.
- Web site: Sciuridae - squirrels, chipmunks, marmots, prairie dogs . . nhpbs.org/ . New Hampshire's PBS Station . 11 July 2023 . Most species eat nuts and seeds. Some species may also eat fungi, insects, eggs, and small vertebrate animals..
- Web site: Callosciurus prevostii . Hoffman . H. . 2003 . animaldiversity.org . Animal Diversity Web . 11 July 2023.
- Shihan . Tahsinur R. . Food Habits of Northern Palm Squirrel Funambulus pennantii Wroughton, 1905 in Chuadanga District, Bangladesh. . Small Mammal Mail . 5 . 1 . 2003 . 14–15 . 11 July 2023.
- Book: Busher . P. . The Encyclopedia of Mammals . Hartman . G. . . 2001 . 978-0760719695 . MacDonald . D. W. . 2nd . 590–593 . Beavers.
- Web site: Heteromyidae: kangaroo rats, pocket mice, and relatives . Myers, Phil . ADW: Animal Diversity Web . University of Michigan: Museum of Zoology . 2013-09-15.
- Web site: Heteromyidae: Kangaroo Rats & Pocket Mice . Merlin, Pinau . Arizona-Sonoro Desert Museum . 2013-09-15.
- Web site: Geomyidae . Myers . P. . 2001 . animaldiversity.org . Animal Diversity Web . 11 July 2023.
- Web site: Lagomorph . www.britannica.com . 3 June 2023 . Britannica . 11 July 2023.
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- Freeman . Patricia W. . Nectarivorous feeding mechanisms in bats . Papers in Natural Resources . 20 September 2006 . 12 July 2023.
- Parolin . Lays Cherobim . Lacher . Thomas E. . Bianconi . Gledson Vigiano . Mikich . Sandra Bos . Frugivorous bats as facilitators of natural regeneration in degraded habitats: A potential global tool . Acta Oecologica . Elsevier BV . 111 . 2021 . 10.1016/j.actao.2021.103748 . 103748. 2021AcO...11103748P . 237717416 .
- Web site: Old World fruit bat . www.britannica.com . 31 May 2023 . Britannica . 11 July 2023.
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- Web site: Phyllostomidae . www.britannica.com . Britannica . 11 July 2023.
- Web site: Phyllostomidae . Burns . L. . Hutzley . V. . Laubach . Z. . 2014 . animaldiversity.org . Animal Diversity Web . 12 July 2023.
- Emons . Louise H. . 2012 . The maned wolves of Noel Kempff Mercado National Park. . Smithsonian Contributions to Zoology . 639 . 1–35 . 10.5479/si.00810282.639 . 12 July 2023.
- Motta-Junior . J. C. . Talamoni . S. A. . Lombardi . J. A. . Simokomaki . K. . Diet of the maned wolf,Chrysocyon brachyurus, in central Brazil . Journal of Zoology . Wiley . 240 . 2 . 1996 . 10.1111/j.1469-7998.1996.tb05284.x . 277–284.
- Quote: "Bamboo forms 99 percent of a panda's diet", "more than 99 percent of their diet is bamboo": p. 63 of Book: Lumpkin . Susan . Seidensticker . John . Giant Pandas . Collins . London . 2007 . 978-0-06-120578-1 . (as seen in the 2002 edition).
- Peyton . B. . Ecology, Distribution, and Food Habits of Spectacled Bears, Tremarctos ornatus, in Peru . Journal of Mammalogy . Oxford University Press . 61 . 4 . 19 December 1980 . 10.2307/1380309 . 639–652 . 1380309 . Non-plant items made up 4.1% of the total scat volume.
- Baldwin . Roger A. . Bender . Louis C. . Foods and nutritional components of diets of black bear in Rocky Mountain National Park, Colorado . Canadian Journal of Zoology . Canadian Science Publishing . 87 . 11 . 2009 . 10.1139/z09-088 . 1000–1008.
- Graber . David M. . White . Marshall . Black Bear Food Habits in Yosemite National Park . Bears: Their Biology and Management . International Association for Bear Research and Management . 5 . 1983 . 3872514 . 1–10 . 10.2307/3872514 . 12 July 2023.
- Bull . E.L. . Torgersen . T.R. . Wertz . T.L. . The importance of vegetation, insects, and neonate ungulates in black bear diet in northeastern Oregon . Northwest Science . 75 . 3 . 1 January 2001 . 244–253 . 12 July 2023.
- Juárez-Casillas . Luis Antonio . Varas . Cora . Evaluation of black bear (Ursus americanus) diet and consequences in its conservation in Sierra de Picachos, Nuevo León, Mexico . Revista Mexicana de Biodiversidad . Universidad Nacional Autonoma de Mexico . 84 . 3 . 2013 . 10.7550/rmb.33376 . 970–976. free .
- McLellan . B.N. . Implications of a high-energy and low-protein diet on the body composition, fitness, and competitive abilities of black (Ursus americanus) and grizzly (Ursus arctos) bears . Canadian Journal of Zoology . Canadian Science Publishing . 89 . 6 . 2011 . 10.1139/z11-026 . 546–558.
- Steinmetz . Robert . Garshelis . David L. . Chutipong . Wanlop . Seuaturien . Naret . Foraging ecology and coexistence of Asiatic black bears and sun bears in a seasonal tropical forest in Southeast Asia . Journal of Mammalogy . Oxford University Press . 94 . 1 . 2013 . 10.1644/11-mamm-a-351.1 . 1–18. 85684360 . free .
- Huygens . Oscar C. . Miyashita . Toshiro . Dahle . Bjørn . Carr . Meghan . Izumiyama . Shigeyuki . Sugawara . Takashi . Hayashi . Hidetake . Diet and Feeding Habits of Asiatic Black Bears in the Northern Japanese Alps . Ursus . International Association for Bear Research and Management . 14 . 2 . 2003 . 3873023 . 236–245 . 12 July 2023.
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- Sethy . Janmejay . Chauhan . Netrapal P. S. . Dietary preference of Malayan sun bearHelarctos malayanusin Namdapha Tiger Reserve, Arunachal Pradesh, India . Wildlife Biology . Wiley . 2018 . 1 . 2018 . 10.2981/wlb.00351 . 1–10. 91990376 . free .
- Kays . R. W. . Food Preferences of Kinkajous (Potos flavus): A Frugivorous Carnivore . Journal of Mammalogy . Oxford University Press . 80 . 2 . 20 May 1999 . 10.2307/1383303 . 589–599. 1383303 . free .
- Kays . R. W. . The behavior and ecology of olingos (Bassaricyon gabbii) and their competition with kinkajous (Potos flavus) in central Panama . Mammalia . Walter de Gruyter GmbH . 64 . 1 . 2000 . 10.1515/mamm.2000.64.1.1 . 1–10. 84467601 .
- Panthi . Saroj . Coogan . Sean C. P. . Aryal . Achyut . Raubenheimer . David . Diet and nutrient balance of red panda in Nepal . The Science of Nature . Springer Science and Business Media LLC . 102 . 9–10 . 28 August 2015 . 10.1007/s00114-015-1307-2 . 54. 26315537 . 2015SciNa.102...54P . 253637154 .
- Web site: Nandinia binotata (Gray, 1830) . . GBIF.org . GBIF . 12 July 2023 . In Gabon, average stomach content was about 80 % fruit and 20 % diverse prey items..
- Allam . Myka S. . Balon . Jan Lloyd I. . Fernandez . Desamarie Antonette P. . 2019 . Diet of Arctictis binturong (Viverridae, Carnivora) in Aborlan, Palawan, Philippines . Journal of Nature Studies . 21 . 1 . 1–9 . 12 July 2023.
- Mudappa . Divya . Kumar . Ajith . Chellam . Ravi . Diet and Fruit Choice of the Brown Palm Civet Paradoxurus Jerdoni, a Viverrid Endemic to the Western Ghats Rainforest, India . Tropical Conservation Science . SAGE Publications . 3 . 3 . 2010 . 10.1177/194008291000300304 . 282–300. 56356587 . free .
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- Kessler . Winifred B. . Kasworm . Wayne F. . Bodie . Walter L. . Three Methods Compared for Analysis of Pronghorn Diets . The Journal of Wildlife Management . Wiley, Wildlife Society . 45 . 3 . 1981 . 3808694 . 612–619 . 10.2307/3808694 . 13 July 2023.
- Wang . Wenxia . Zhou . Ran . He . Lan . Liu . Shuqiang . Zhou . Juntong . Qi . Lei . Li . Linhai . Hu . Defu . The progress in nutrition research of musk deer: Implication for conservation . Applied Animal Behaviour Science . Elsevier BV . 172 . 2015 . 10.1016/j.applanim.2015.09.006 . 1–8.
- Book: Bertelsen, Mads F. . Fowler's Zoo and Wild Animal Medicine, Volume 8 . Giraffidae . Elsevier . 2015 . 10.1016/b978-1-4557-7397-8.00061-x . 602–610. 9781455773978 . 215746046 .
- Cantalapiedra . Juan L. . FitzJohn . Richard G. . Kuhn . Tyler S. . Fernández . Manuel Hernández . DeMiguel . Daniel . Azanza . Beatriz . Morales . Jorge . Mooers . Arne Ø. . Dietary innovations spurred the diversification of ruminants during the Caenozoic . Proceedings of the Royal Society B: Biological Sciences . The Royal Society . 281 . 1776 . 7 February 2014 . 10.1098/rspb.2013.2746 . 20132746. 24352949 . 3871323 .
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- Web site: Baubet . Eric . Bonenfant . Christophe . Brandt . Serge . Diet of the wild boar in the French Alps . ResearchGate . 16 . 30 November 2003 . 13 July 2023.
- Web site: Diet studies of Bearded Pigs in Kayan Mentarang National Park, Borneo, Indonesia . Wulffraat, Stephan . 2006 . WWF Indonesia . 13 July 2014.
- Web site: Leus . Kristin . Morgan . C A . Analyses of diets fed to Babirusa (Babyrousa babyrussa) in captivity with respect to their nutritional requirements. . Gran Paradiso National Park . 2005 . 13 July 2023.
- Book: Ecology, Conservation and Management of Wild Pigs and Peccaries . Cambridge University Press . 21 November 2017 . 978-1-316-94123-2 . 10.1017/9781316941232 . Melletti . Meijaard . Mario . Erik .
- Web site: Hylochoerus meinertzhageni (Giant) Forest Hog . d'Huart, J. . Kingdon, J. . 13 July 2014.
- Treydte . Anna C. . Bernasconi . Stefano M. . Kreuzer . Michael . Edwards . Peter J. . Diet of the Common Warthog (Phacochoerus africanus) On Former Cattle Grounds in a Tanzanian Savanna . Journal of Mammalogy . Oxford University Press . 87 . 5 . 2006 . 10.1644/05-mamm-a-336r2.1 . 889–898. 84114930 . free .
- M . Altrichter . JC . Sáenz . E . Carrillo . TK . Fuller . Seasonal diet of Tayassu pecari (Artiodactyla: Tayassuidae) in Corcovado National Park, Costa Rica . Revista de Biología Tropical . 2000 . Rev Biol Trop . 48 . 2–3 . 689–701 . 11354977 . 13 July 2023 .
- Web site: Camelidae . Myers . P. . 2000 . animaldiversity.org . Animal Diversity Web . 13 July 2023.
- Web site: Hippopotamus amphibius . Mason . K. . 2013 . animaldiversity.org . Animal Diversity Web . 13 July 2023.
- Hendier . Alba . Chatelain . Cyrille . Du Pasquier . Pierre-Emmanuel . Paris . Monique . Ouattara . Karim . Koné . Inza . Croll . Daniel . Zuberbühler . Klaus . A new method to determine the diet of pygmy hippopotamus in Taï National Park, Côte d'Ivoire . African Journal of Ecology . Wiley . 59 . 4 . 9 June 2021 . 10.1111/aje.12888 . 809–825. 10023/25508 . 236293333 . free .