TAXONOMY & NOMENCLATURE
(McKenna & Bell 1997) (Mead et al 2007)(Rowe & Honeycutt 2002) (Wilson & Reeder 2005) (Wyss. et al 1993) (Kurtén & Anderson 1980)
Describer (Date): Linnaeus, 1766. Systema Naturae, 12th ed., 1:103
for Hydrochoerus hydrochaeris
Goldman, 1912. Smithsonian Miscellaneous Collection, 60(2):11 for H. isthmius
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Rodentia
Family: Hydrochoeridae
Genus: Hydrochaeris - Brunnich 1772
Species: Hydrochaeris hydrochaeris
Species: H. isthmius
Taxonomic History and Nomenclature
- Traditional classifications consider capybara to be in its own family, the Hydrochoeridae
- Recent genetic studies place Hydrochaeris within Caviidae, the family which includes cavies, maras and guinea pigs
- Much uncertainty regarding how capybara relate to other South American rodents
- H. isthmius a distinct species with karyotype 2n-64 and FN=104 (Mones 1991) but not recognized as separate species by other researchers (Flynn 2008)
Common Name
- Some 190 local common names most of native origins
- Kapiyva or "master of the grasses" in Amazon tribe's native language
- In Spanish: carpincho, capibara, chigüiro, maja, poncho
Scientific Name
- From Greek Hydro chaeris meaning "water hog"
Phylogeny
- Ancestors of modern capybara: cavy-like rodents (cavimorphs)
- Late Eocene to Early Oligocene (37.5 to 31.5 million years ago), Chilean Andes
- Cavimorphs perhaps arrived in South America from Africa
- True capybaras first recorded in Argentina about 9 million years ago
- As many as 56 separate fossil species, most described solely on basis of teeth
- But teeth change shape significantly as a capybara ages
- In actuality, not so many species
- Revision needed
- About 3.5 million years ago, capybara dispersed to North America across the Panamanian land bridge
- During the Pleistocene Ice Ages, capybara lived in southern U.S.
- Pleistocene fossil sites of Neochoerus pinckneyi (40% larger than modern capybara) in Florida, South Carolina, Texas
- Pleistocene fossil discovered in 1995 from Ice Ages pond sediments, San Diego County, California (Deméré 2007)
- In Pleistocene, capybara often associated with bizarre, large armored glyptodonts in wet habitats
- Only one genus and one (or two) species living today
DISTRIBUTION & HABITAT
(Herrera & Macdonald 1989) (Mones & Ojasti 1986) (Verdade &. Ferraz 2006)
Distribution
- Prehistoric distribution: North America, Central America, West Indies, South America
- Historically (before livestock introduced): riparian regions throughout South and Central America.
- Currently for H. isthmius: eastern Panama and northern coastal Colombia and Venezuela
- Currently: for H. hydrochaeris: northern South America east of the Andes from Panama to NE Argentina
- Portions of Columbia, the Guianas, Suriname
- Paraguay and Uruguay
- Northeastern Argentina
- Amazonian Ecuador, Peru, and Bolivia
- Concentrations in:
- Llanos of Venezuela
- Pantanal wetlands of western Brazil
- Taim lowlands of southern Brazil

Habitat
- Lowlands from open plains to tropical rain forests, always near water
- Swampy, marshy, grassy areas bordering rivers, ponds, streams, lakes
- Prefer nutrient-rich muddy rivers with aquatic grasses
- Need extensive meadows at low water times
- Considered a habitat specialist
- Use open water for drinking, wallowing, predator protection
- Use dry land for foraging, resting
- Grassy patches and brushy scrub both essential in extremes of dry and wet seasons
- Ecology largely unknown until 1966 when Venezuelan government began studies in Llanos region
PHYSICAL CHARACTERISTICS
(Herrera 1992) (MacDonald 1984) (Mones & Ojasti 1986) (Pereira et al 1980) (Nowak 1999)
Body Weight: Average adult 48.9 kg (108 lb); 35 to 65.5 kg (77 lb to 144 lb) in Venezula's Llano region; a record 91 kg (200 lb) in southern Brazil
Head/Body Length: 106 to 134 cm (42 to 53 in);
Shoulder Height: 60.9 cm (2 ft.)
Tail Length: Tail vestigal
General
- Largest living rodent
- Resembles a cavy but larger, with shorter body
- Barrel-shaped body
- Heavy, blunt muzzle
- Cheek teeth ever-growing
- Spends much time in water
- Eyes and small ears set high on head (can be alert while nearly underwater)
- Able to stay completely under water several minutes
- Slightly webbed toes (four on the front, three on the back)
- Water immersion helps capybara regulate body temperature
- Front legs shorter than rear legs
- Nails strong, hoof like
- Body size and mass increases with a population's increased latitude
Pelage and Skin
- Hunted for pelts in historic times
and managed on ranches today
- Between 1960 and 1969, 1.5 million skins exported from Brazil
- Coloration generally reddish brown to grayish on upper parts, yellow-brown on undercarriage; some black on the face, outer limbs and rump
- Long, course, and sparse hair may help this water-loving animal
dry when out
of water
- Thin hair makes sunburn a problem; mud caked on hair offers protection
- Low number of sweat glands in skin plus large body size make thermal stress a problem
Sexual Dimorphism
- Males more massive than females with similar length
- Males have large visible scent gland (the morrillo) on top of snout
- Morrillo used to rub on vegetation to mark territory
- May function also as status signal
- Larger morrillos associated with larger testes and greater sexual activity
- Females have same gland, but underdeveloped
Other Physical Characteristics
- Teeth of capybara grow throughout life in all dimensions; cutting and grinding surfaces become more complex as animal ages
BEHAVIOR & ECOLOGY
(Lord-Rexford 1994) (Herrera & Macdonald 1989, 1993)
(Macdonald 1981a, b) (Nowak 1999) (Ojasti 1991) (Rowe and Honeycutt 2002)(Tomazzoni et al 2005)
Activity Cycle
- Resting close together at water's edge in morning
- Most grazing late afternoon and evening; graze in short sessions at night
- Rest in water or mud during the heat of the day
- After disturbances from humans, more nocturnal and shy
- Group size fluctuates with wet/dry seasons
Territory Size
- Territories remain very stable for several years
- Along rivers groups space themselves from 100 to 500 m (.06 to .3 mi.) apart
- Groups may occupy a home range from 2 to 200 hectares (4.9 to 494 acres)
- Average group uses 5 to 20 hectares (12.4 to 49.4 acres)
- In one study, each group used a home range averaging about 79 hectares and defended a territory of 9 hectares
- Density of capybara within their territories quite high compared to other tropical herbivores of similar size
- Biomass of capybara 10 times greater than similar sized grazing Bohr's reedbucks' biomass
- Density of capybara populations reflects high primary productivity of savanna habitats in Llanos of Venezuela
Social Groups
General
- Social animals living in groups
- Dry season: up to 100 individual at water sources
- Wet season: group size up to 40 individuals
- Bonds between animals maintained by touching, grooming, scent marking, vocalizations
- High levels of sociality possibly a response to risk of predation and resource availability
- Capybara similar in this trait to South American desert and rock cavies and maras
Hierarchy
- Herds with dominant and subordinate males plus females and young
- Typical make-up of breeding groups: one male & 4 to 14 females
- Dominance positions very stable, lasting for years
- Dominant male may claim access to best water holes, parasite-eating birds, and females in estrus
- Largest males are usually dominant individuals
- Size not a factor in status among subordinate males
- Subordinate males tend to occupy positions on edges of resting groups, away from dominant male
- No bachelor groups
- Males not in groups have little protection from predators
- Outside the group, no chance for reproduction
Territorial Behavior
- Groups occupy territories that are defended
- Exception to this rule: quick unchallenged passage by neighboring capybara to reach distant territory
- Capybara bark at intruders, then if necessary, jump in river or run away
- Both sexes scent-mark using anal glands
- This behavior may also play a role in defining territories
Aggression
- Grooming lessens tension between individuals and removes parasites
- Male aggression more frequent with increasing numbers of males in group
- Harassment and chasing: main form of male/male aggression
- Subordinate males rarely retaliate
- Retaliation involves facing opponent, both animals rushing towards each other, rearing on hind legs, grappling, loser fleeing
- Subordinate males often suffer serious bites to rump as they flee
- Most commonly, dominant male walks, nudges, or "escorts" subordinate male to edge of group
Play
- Young in groups play in water, imitate males
- Like other cavy-like social rodents, individuals chase each other, play-wrestle, gallop
Communication
Visual Signs
- Greatly enlarged scent glands on top of snout in male signals status & may attract females
- Size of male's morrillo a sign of rank
- Amount of scent-marking correlates with dominance rank
Vocalization
- Infants and young constantly emit a guttural purr, perhaps to stay in touch with group; losers in aggressive matches also make this sound in appeasement
- Low clicking sounds of contentment
- Sharp prolonged whistles, squeals, short grunts
- Alarm bark or cough
- Most warning calls come from subordinate males in a group; companions react by standing alert or plunging into nearest water
- Females emit a whistle when in estrus
- Males tooth-chatter as sign of aggression
- Many other closely related species also highly vocal, especially guinea pigs and cavies
Olfaction/Scent Marking
- Both sexes scent mark with anal gland; females less frequently
- Group members may recognize each other by their unique mix of scent chemicals
Locomotion
- Excellent swimmer; good diver, can stay underwater for up to 5 minutes
- Move from place to place in short bursts of travel not more than 200 m. (.12 mi.) with long rests between
- Walks, grazing, in typical day about 700 m (.43 mi)
- Star-shaped footprints
- Rather sedentary habits allow ranchers to manage capybara without fences
- Several juveniles may ride on female's back as she swims
Interspecies Interaction - Puma & jaguar
prey on capybara
- When attacked by wild dogs, capybara group forms defensive huddle with young in center, adults facing outwards
- Juveniles preyed upon by foxes, ocelots, cayman, raptors, occasional possums (attacking infants), anaconda
- Co-exist with domestic cattle
- At least nine species of birds increase their feeding rate by associating with capybara
- Especially jacana, scarlet ibis, sharp-tailed Ibis, white Ibis, buff-necked ibis, swifts
- Egrets hunt from moving and stationary capybara's backs
- Swifts hunt low overhead or from capybara's head
- Researcher observed capybara soliciting tick-eating (Amblyomma spp.) by yellow-headed caracara
- Five bird species associated with capybara in order to find food. (Tomazzoni et al 2005)
- Southern caracara, rufous hornero, cattle tyrant, yellow-headed caracara, shiny cowbird
- Strategies of the birds included using the capybara as a perch, walking with the capybara to catch flushed prey, foraging in capybara skin
DIET & FEEDING
(Barreto and Herrera 1998) (Borges & Colares) (Nowak 1999) (Quintana et al 1998)
Anatomy and Physiology
- Digestive system similar to rabbit's
- Simple stomach
- Large intestinal pouch (caecum) with microorganisms for fermenting cellulose
- Excrete two kinds of feces
- Olive colored oval balls
- Also colorless, protein rich "paste" which is re-ingested for maximum digestion of nutrients (= coprophagy)
- Regurgitate and re-chew food while resting
- Front incisors crop native grasses too short for cattle
Feeding Strategies and Food Items
- Are selective grazers; eat approximately 3 kg/day fresh forage, mainly grasses
- Tend to be more selective when more plant species available
- 80% of diet is only 5 species of grasses (Poaceae)
- Most common plant species in areas typically the ones eaten most often, especially in winter when fewer species available
- Various estimates for amount of aquatic plants in diet from .6 % to 87 %
- As wet season advances, more reeds and water hyacinths consumed
- Capybaras raid cultivated fields for grains, melons, squashes, bananas, sweet potatoes, manioc leaves and corn
REPRODUCTION & DEVELOPMENT
(Macdonald and Herrera 2001) (Nogueira et al 1999) (Ojasti. 1968) (Paula et al 1999) (Rowlands and Weir 1974) (Weigl 2005)
Courtship
- Female estrus cycle: every 7.5 days; remain receptive only 8 hours
- In mating season, dominant males conspicuously guard females
- When female in estrus, dominant male sniffs her frequently
- Female whistles when in estrus to attract males
- Mating season year round with peak at beginning of wet season
Reproduction
- One litter/yr; two litters possible under good conditions
- Harem-based polygynous breeding (one dominant male, several females)
- Female pursued by male enters water and swims back and forth
- Pair mates in water; female often submerged for brief copulation
- Females not wanting to mate may dive deep enough to dislodge male
- Mating pair often interrupted by a second male
- Life span of male's sperm longer than that in most rodents; capybara mating system promotes sperm competition
- Group association essential for raising young; groups smaller than four adults fail to rear any young
Gestation
Life Stages
Birth
- 4 to 5 pups most common; a breeding group may have 15 pups or more at one time
- At birth young weigh about 1,500 grams (3.3 lb)
- At birth all cheek teeth already erupted, with signs of wear
(Kramarz
2002)
- Young can follow mother and eat grass shortly after being born (are precocial)
- Young nurse about 16 weeks
Infant (< 1 year old)
- Young may suckle indiscriminately from several females;
- Small groups of young move about herd, nudging females until one stands to allow nursing
- Very young ride on females' backs'
- Very young avoid water where caimen and anaconda lurk
- Females spend a lot of time caring for young of different ages
Juvenile
- Yearlings disperse from parents' group
Subadult
- By 18 mos. weigh about 40 kg (88 lb.)
Adult
- Females sexually mature age 7 to 12 mos.
- Males between 15 and 24 mos.
Longevity
- Average life span 7-10 years;
- In captivity in the Adelaide Zoo in Australia, 15 years
- One H. isthmius at the San Diego Zoo: 9 years, 6 mos.
Mortality
- Preyed upon by foxes, bush dogs, feral dogs, ocelots, cayman, jaguars, eagles, caracaras, black vultures and human hunters
- Wild capybara, especially in Venezuela, are poached and illegally hunted more intensely in the weeks before Easter, when they are a sanctioned by the Catholic Church as a substitute for fish (because of their semi-aquatic habits).
- Jaguars prey most often on young males at the periphery of the group (and furthest from the water)
- Infanticide in captive populations, but not in wild
DISEASES AND PATHOLOGY
(Labruna et al 2004, 2007) (Lord & Flores 1983)(Mones & Ojasti 1986) (Meireles et al 2007) (Saraiva 2004)
Diseases & pathogens in wild capybara
- Parasites include species of intestinal protozoa (Ciliata), spore-producing parasitic protozoa (Apicomplexa), parasitic worms or flukes (Trematoda), tapeworms (Cestoda), roundworms (Nematoda), insects and fungi.
- Rare case of natural infection with avian eye trematode Philophthalmus lachrymosus;
- This parasite also infects humans
- Carry Cryptosporidium, a protozoa causing gastro intestinal infections in humans;
- Safety of human water supplies near capybara
populations is a concern
- Bites and massive lesions from Amblyomma (Ixodidae) ticks carrying Rickettsia rickettsii bacteria
- This pathogen responsible for Brazilian Spotted Fever in humans
- In southeastern Brazil incidence this disease may be rising due to capybara populations moving into urban areas (and vice versa)
- Blood studies show capybara may host two species of a Brucella bacteria, B. suis and B. abortus
- Infect pigs and cattle
- Symptoms of this disease in capybara not known
- Carry a parasitic protosoa, Trypanosoma evansi
- Some capybara with the parasite appear in perfect health; others show signs of weight loss, apathy, lack of coordination of hindlimbs, hair loss, eye infections, enlarged spleen, death
- T. evansi reported in capybara populations in Argentina, Brazil, Panama, Paraguay
- T. evansi causes disease of horses and wildlife ("mal de caderas" in Argentina)
- Most common in first half of wet season when prolonged flooding reduces available habitat
- Anecdotal reports that trypanosomiasis is milder for horses living in areas where capybara are common
Diseases In Captivity
- Mange or scabies from mites (Sarcoptes scabiei), a common skin problem in animals without water access
- Wounds from male-male aggression a problem
- Scurvy in animals without source of Vitamin C
- Symptoms included bleeding gums and noses, tooth loss, fragile bones, disruption of reproduction in males and females, death
- Can be experimentally infected with foot-and mouth disease, but natural infection not known
MANAGED CARE
(Chapman 1991) (Nogueira et al 1999)
Captive Breeding
- Zoo-raised capybara have higher survival rate than those in wild
- Females in captivity reach sexual maturity later than in wild (26 vs. 18 months)
- Capybaras bred in many zoos and also commercially for meat and skins in South America
- Some populations managed in natural areas
- Problems with enclosed or penned individuals
- Male/male aggression when overcrowded
- Hierarchical group social structure disrupted when new individuals introduced
- Infanticide by female pen mates
- Females' lack of experience not a factor
- No infanticide when females have been raised together (are familiar with each other)
- No aggression by females except at birth of pen mate's young
POPULATION AND CONSERVATION STATUS
(Moreira & Macdonald,1996) (Ojasti 1991) (Verdade & Ferraz 2006)
Population Density
- 195 individuals/sq. km. ( 0.4 sq. mi) in southeastern Brazil wetlands
- Between 10 and 200 individuals/ sq. km.(0.4 sq mi) in Venezuelan llanos
- Status in all areas depends on management practices
- Some areas allow controlled harvest and tolerate subsistence hunting
- Elsewhere all hunting prohibited but poaching may be common
- Protections enforced in other areas
- Management for cattle may improve habitat for capybara
- Populations considered a potential nuisance in east central Sao Paulo Brazil where they often live near humans
- Blamed for crop damage
- Associated with Brazilian Spotted Fever
Conservation
1953: Hunting regulated in Venezuela
1967: Hunting prohibited in Brazil (Federal Law No. 5.197) but harvesting being considered to reduce population densities and impact on agriculture in some areas
1968: Venezuela develops management plan using studies of capybara biology and ecology
1980: Hunting prohibited in Columbia
2000: Central Suriname Nature Reserve established on North Atlantic coast of South America; 1.592 million hectares (
6,146 sq mi.)
- IUCN Status 2006:
Lower Risk; Conservation Dependent (1C).
- Locally common; farmed for meat and skin in some areas
- CITES Status:
Not listed
Threats to survival
-
Status not threatened at present, but habitat loss and hunting/farming need controls
and monitoring
- Predators' declines due to habitat loss may offer short-term benefit to capybara populations
- Hunting often removes larger and older individuals from population (large males, pregnant females)
and reduces group size
- Long-term effect: decrease in body size of hunted population
- Smaller groups mean fewer young survive per female
- Hunting drives normally savanah-dwelling animals to forested habitats where resources are not optimal
- Encroachment of human development
- Clear-cutting/burning, farming
- Human perception of their role in competing with cattle for food, as pests of sugarcane and rice mono cultures, or as carriers of diseases
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