Geographic Range
White-bellied caiques, or green-thighed parrots (
Pionites leucogaster
) are native to South America. Their geographic range stretches from the Atlantic
Ocean near Belem, Brazil to central South America. White-bellied caiques are most
commonly found within Brazil, south of the Amazon River. They have been observed in
the Brazilian states of Mato Grosso, Para, from the Madeira River to the Purus River,
and from Jurua River to the South American countries of Ecuador, Peru, and Bolivia.
- Biogeographic Regions
- neotropical
Habitat
White-bellied caiques live in terrestrial lowland tropical rainforests and terra firme
forests. However, they are more commonly found in varea forests. These forests are
prone to flooding and have high humidity, which provide ideal habitat for white-bellied
caiques. These parrots are more commonly found in trees that border watercourses.
During the breeding season, they reside in hollow trees approximately 30 m above the
forest floor. Average elevation for these habitat types are around 800 m. White-bellied
caiques do not migrate seasonally.
- Habitat Regions
- tropical
- terrestrial
- Terrestrial Biomes
- rainforest
Physical Description
White-bellied caiques are short, stout parrots approximately 23 cm long, with a wingspan of 38 cm, and weighing an average of 165 g. They have white, hooked beaks with pink nostrils on their ceres, a patch of bare skin above bird beaks. They also have bare skin around their eyes, which may possess melanistic spots or red irises surrounded by grey rings. White-bellied caiques are zygodactyls, meaning they has two toes facing forward and two more directly opposite facing backwards. Their tails are square in shape.
They have orange feathers on their heads and necks are orange, bright yellow on their cheeks, and white on their ventral side. These birds have a green lower belly, legs, back feathers, and underwings, dark blue wing coverts, and blackish flight wings.
Two subspecies of white-bellied caiques exist: Pionites leucogaster xanthurus and P. l. xanthomeria . Pionites leucogaster xanthurus has paler colorations and P. l. xanthomeria has yellow thighs.
White-bellied caiques are not sexually dimporhic and require DNA analyses or blood
samples to determine sex. Immature white-bellied caiques are often confused with black-headed
caiques (
Pionites melanocephalus
) because of the black juvenile feathers on their heads. In 6 to 24 months, they molt
these black feathers.
- Other Physical Features
- endothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
Reproduction
Little is known about reproductive and nesting behaviors of white-bellied caiques.
They have been observed to be monogamous, with no known courtship behaviors. However,
paired white-bellied caiques participate in feeding and grooming one another before
mating. Eggs must be laid within 48 hours after copulation to be fertile. During the
breeding season, white-bellied caiques copulate daily, usually more than once a day.
- Mating System
- monogamous
Reproductive behavior is driven by environmental and seasonal factors, such as temperature, photoperiod, rainfall and humidity. White-bellied caiques have their breeding season from October to April in the Amazon, but they have been recorded in outdoor captivity (southern Florida) to mate from early January to June. Parrots breed once per year. Both males and females reach sexual maturity around two to three years of age and lay their first clutch by their third year, although one case showed egg-laying by the age of 11 months with unknown causes. White-bellied caiques have an average clutch size of 3 small white eggs, approximately 2.5 cm in width and 3.2 cm in length. Females lay one egg every 2 to 3 days.
In captivity, white-bellied caiques are prolific breeders, with clutch sizes of up
to 6. In captivity, breeding pairs use nest boxes; females remains inside, incubating
eggs for 26 days while their mates feed them. Chicks are born blind with sensitivity
to light and only a few downy feathers, weighing an average of 7.2 g.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Female white-bellied caiques sit on eggs until hatching. Male white-bellied caiques
bring their female mates food and provide protection during this time. After chicks
hatch, both parents take turns caring for their young. Usually, females regurgitate
digested food to feed the chicks. Parents stay with chicks through their fledgling
stage, about 11 to 12 days after being born.
- Parental Investment
- altricial
- male parental care
- female parental care
-
pre-hatching/birth
-
protecting
- female
-
protecting
-
pre-weaning/fledging
-
protecting
- female
-
protecting
Lifespan/Longevity
An average lifespan for wild white-bellied caiques is currently unknown. In captivity,
the species has been recorded to have a maximum longevity of 26 years, but is expected
to have the potential of living up to 40 years.
Behavior
In captivity, white-bellied caiques are known as the clowns of the parrot community. They exhibit playful behaviors such as hopping or frequently lying on their backs. Due to their high cognitive ability, they can be taught tricks; however, they generally lack the ability of vocal learning and are not known to imitate human languages.
White-bellied caiques live and travel in pairs or monospecific family groups of 10 or more. Their groups congregate in the forest canopy, spending most of the day feeding and resting. They participate in preening behaviors and are generally highly sociable during resting periods. While in flight, these birds fly low through the canopy, unlike many other parrot species, they fly without vocalizing.
White-bellied caiques occupy clay licks during feeding times, where predation and
competition influence their behavior. They have been observed to join small parrot/parakeet
aggregations rather than large parrot or macaw aggregations. White-bellied caiques
benefit from large mixed species groups, which serves as protection from nearby predators.
This species displays two approach behaviors while attending clay licks. They either
arrive in slow, circular flight patterns or they move deliberately through adjacent
trees to check for predators or landslides and search for other individuals to lead
the group. If a group spots any threats, or are not joined by other individuals, that
group will cease its approach or move to alternative areas.
Home Range
Currently, an exact home range or territory size for white-bellied caiques is unknown.
Communication and Perception
White-bellied caiques communicates mainly using vocalizations. Their call consists
of screeches, shrieks and squawks. In the wild they are very noisy, vocalizing repeatedly
while resting and in flight. Reports note that, in captivity, noisiness is dependent
upon the individual bird. White-bellied caiques can mimic, or imitate environmental
sounds, but cannot repeat human speech. Aside from their keen sense of hearing, white-bellied
caiques also perceive their environment through its senses of touch, taste, and sight.
They use their tongue to feel and taste their surroundings by repeatedly licking an
object. Like all bird species, white bellied caiques have four types of color-receptive
cones which allow them to distinguish colors humans cannot perceive. Three of their
cones are detect a spectrum of color similar to the human-visible spectrum, but with
a slightly more limited range of wavelengths. Their cones also have specially adapted
oil droplets that allow them to better distinguish colors by refining specific wavelengths.
Their fourth cone is ultraviolet sensitive, which allows them to see in the UV spectrum.
- Communication Channels
- acoustic
- Other Communication Modes
- mimicry
Food Habits
The diet of white-bellied caiques consists of a variety of fruits, vegetables, flowers,
low amounts of clay lick, and occasionally ants. Clay licks provide a sodium supplement
and protect white-bellied caiques from harmful dietary toxins, so it is an important
part of their diet. Lee et al. (2014) observed food consumption for a population
of caiques and found that an average diet consisted of 24% flowers, 34% seeds, 31%
pulp and 11% whole proportions of flowers, fruit pulp, seeds, and entire fruit in
the diet. The study also reported that this bird consumed 44 unique plant species
over the course of the study. Its diet is high in carbohydrates and fats for daily
energy expenditures, such as thermoregulation, body growth, and maintenance. They
consume additional protein during breeding season to promote egg health and nestling
growth. Offspring eat regurgitated food from their parents and have to eat often
– about every 1 hour, though that time lengthens with age.
White-bellied caiques select foraging sites based on food supply. They forage on the
forest floor and in the canopy in mornings due to the good lighting and cooler temperatures.
These parrots have two bouts of feeding each day — once in the morning and once in
the late evening. They use their stout legs and zygodactyl toe arrangement to hang
from tree branches and feed, using one of their feet to grab and bring food to their
beaks. White-bellied caiques have highly sensitive tongues, which they use to probe
nuts or seeds, searching for a crease or groove. They search for the most effective
entry site, then use their beaks to crack open and eat nuts or seeds. White-bellied
caiques hone, sharpen, and clean their beaks by chewing on wooden branches. This special
food behavior keeps the beak in good condition and exercises pivotal jaw muscles.
- Plant Foods
- seeds, grains, and nuts
- fruit
- nectar
- flowers
Predation
Because there are few scientific studies on white-bellied caiques, their predators
are unknown. However, they are a target of anthropogenic trapping and hunting. Because
they can fly, they are intelligent, and they live in large groups, most Amazonian
parrots do not have many predators. Potential predators include birds of prey, monkeys,
and snakes, which usually target eggs rather than mature parrots.
Ecosystem Roles
Because a significant amount of their diet is fruit, white-bellied caiques act as seed dispersers in their environment. They compete with other Amazonian parrot species for feeding and nesting habitats. They compete with blue-headed parrots ( Pionus menstruus ), orange-cheeked parrots ( Pyrilia barrabandi ), dusky-headed conures ( Aratinga weddellii ), and white-eyed conures ( Psittacara leucophthalmus ).
Like many other species in the order
Psittaciformes
, white-bellied caiques sometimes suffer from skin and feather disorders caused by
parasites, such as lice, mites, fleas, bacteria, viruses, and fungi. Parasitic infections
are common amongst birds that were recently imported or that have frequent contact
with the ground.
- Ecosystem Impact
- disperses seeds
Economic Importance for Humans: Positive
White-bellied caiques are purchased as pets, and so they serve as a major source of income for the international pet trade and pet store owners from both legal and illegal trafficking.
The illegal pet trade in Santa Cruz de la Sierra, Bolivia brings in a mass of circulating money. Traffickers face up to two years of imprisonment and a fine up to 100% of the organisms' cost. However, this penalty is rarely enforced, as Santa Cruz officials declare animal trafficking as a low priority offense.
A common disease specific for parrot species like white-bellied caiques is psittacine
beak and feather disease (PBFD). Effects of PBFD include beak and claw deformities,
loss of feathers and/or abnormalities, which result in death by immunosuppression.
Being that white-bellied caiques can carry this disease, it is a common test subject
for genetic research into the evolution of the disease and its host. Blood sampling
from white-bellied caiques is being used as a reference sequence to investigate the
genetic diversity the virus in South African parrots. This may help protection and
conservation efforts for other psittacines around the world.
- Positive Impacts
- pet trade
- research and education
Economic Importance for Humans: Negative
There are no known negative or harmful effects of white-bellied caiques on humans.
Conservation Status
White-bellied caiques are currently listed as an endangered species on the IUCN Red List. The primary threat to white-bellied caiques is increased deforestation and urbanization of the Amazonian basin. The Brazilian Forest Code is a piece of legislation listing the laws involving forestry and landownership in Brazil. Legal changes made to the Brazilian Forest Code have reduced the percentage of natural forestry required for a private landowner to own, making it easier for private landowners to contribute to deforestation. Loss of their habitat combined with poaching has caused a decrease in population.
There are no conservation actions in progress for white-bellied caiques, but there are some conservation actions being proposed. These include the management of new protected areas, the expansion of biodiversity conservation, and the expansion of protected Important Bird and Biodiversity Areas (IBAs), which are restricted areas specifically for bird conservation. There are also campaigns against the changes made on the Brazilian Forest Code.
White-bellied caiques are a social species that can adapt to captive conservation research initiatives indefinitely. This involves constant breeding, artificial incubation, and aviculture. The Palm Beach Zoo at Dreher Park in Florida and the Rare Species Conservatory Foundation partnership developed the White-bellied Caique Population Management Program. Other institutional facilities such as Beardsly Zoological Gardens, Bronx Zoo/Wildlife Conservation Park, and Central Park Zoo (WCS Conservation Center) participate in these captive conservation programs. The success of zoological institutions, private aviaries and the established White-bellied Caique Population Management Program with the genetic database and husbandry protocol serves as a template for a recovery procedure and restoration of wild flocks.
This species, along with all other parrots in
Psittaciformes
, is protected under CITES. White-bellied caiques are listed under Appendix II, which
regulates trade.
Additional Links
Contributors
Jennie Rhambarose (author), Radford University - Fall 2015, Karen Powers (editor), Radford University, April Tingle (editor), Radford University, Cari Mcgregor (editor), Radford University, Zeb Pike (editor), Radford University, Jacob Vaught (editor), Radford University, Galen Burrell (editor), Special Projects.
- Neotropical
-
living in the southern part of the New World. In other words, Central and South America.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- terrestrial
-
Living on the ground.
- rainforest
-
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
- monogamous
-
Having one mate at a time.
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- male parental care
-
parental care is carried out by males
- female parental care
-
parental care is carried out by females
- arboreal
-
Referring to an animal that lives in trees; tree-climbing.
- diurnal
-
- active during the day, 2. lasting for one day.
- motile
-
having the capacity to move from one place to another.
- sedentary
-
remains in the same area
- social
-
associates with others of its species; forms social groups.
- acoustic
-
uses sound to communicate
- mimicry
-
imitates a communication signal or appearance of another kind of organism
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
- pet trade
-
the business of buying and selling animals for people to keep in their homes as pets.
- herbivore
-
An animal that eats mainly plants or parts of plants.
- frugivore
-
an animal that mainly eats fruit
- granivore
-
an animal that mainly eats seeds
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
References
Bird, J., G. Buchanan, A. Lees, R. Clay, P. Develey, I. Yepez, S. Butchart. 2011. Integrating spatially explicit habitat projections into extinction risk: A reassessment of Amazonian avifauna incorporating projected deforestation. Diversity and Distributions , 18/3: 273-281.
BirdLife International, 2014. "Pionites leucogaster" (On-line). The IUCN Red List of Threatened Species 2014. Accessed September 11, 2015 at http://www.iucnredlist.org/details/62181308/0 .
Birdlife International, 2014. "Pionites leucogaster" (On-line). The IUCN Red List of Threatened Species 2014: e.T62181308A62181748. Accessed November 28, 2015 at http://dx.doi.org/10.2305/IUCN.UK.2014-2.RLTS.T62181308A62181748.en .
Brightsmith, D. 2005. Parrot nesting in southeastern Peru: Seasonal patterns and keystone trees. The Wilson Bulletin , 117/3: 296-305.
Buchner, T. 1983. Parrot eggs, embryos and nestlings: Patterns and energetics of growth and development. Physiological Zoology , 56/3: 465-483.
Cameron, M. 2012. Parrots: The Animal Answer Guide . Baltimore, MD: The Johns Hopkins University Press.
De Schauensee, R. 1970. A Guide to The Birds of South America . Philadelphia, PA: The Academy of Natural Sciences of Philadelphia.
Gilardi, J., C. Munn. 1998. Patterns of activity, flocking, and habitat use in parrots of the Peruvian Amazon. The Condor , 100/4: 641-653.
Greiner, E., B. Ritchie. 1994. Avian pathogenic flagellated enteric protozoa. Journal of Exotic Pet Medicine , 4/3: 112-125.
Heath, L., D. Martin, L. Warburto, M. Perrin, W. Horsfield, C. Kingsley, E. Rybicki, A. Williamson. 2004. Evidence of unique genotypes of beak and feather disease virus in southern Africa. Journal of Virology , 78/17: 9277–9284.
Herrera, M., B. Hennessey. 2007. Quantifying the illegal parrot trade in Santa Cruz de la Sierra, Bolivia, with emphasis on threatened species. Bird Conservation International , 17/4: 295-300.
Lee, A., D. Brightsmith, M. Vargas, K. Leon, A. Mejia, S. Marsden. 2014. Diet and geophagy across a western Amazonian parrot assemblage. Biotropica , 46/3: 322-330.
Lee, A., S. Marsden. 2012. The influence of habitat, season, and detectability, on abundance estimates across an Amazonian parrot assemblage. Biotropica , 44/4: 537-544.
Miyaki, C., R. Griffiths, K. Orr, L. Nahum, S. Pereira, A. Wajntal. 1998. Sex identification of parrots, toucans, and curassows by PCR: Perspectives for wild and captive populations studies. Zoo Biology , 17: 415-423.
Parker, III, T. 1982. Observations of some unusual rainforest and marsh birds in southeastern Peru. The Wilson Bulletin , 94/4: 477-493.
Rinder, M., A. Ackermann, H. Kempf, B. Kaspers, R. Korbel, P. Staeheli. 2009. Broad tissue and cell tropism of avian bornavirus in parrots with proventricular dilatation disease. Journal of Virology , 83/11: 5401-5407.
Rodriguez Mata, J., E. Francisco, M. Rumboll. 2006. Birds of South America Non-Passerines: Rheas to Woodpeckers . Princeton, NJ: Princeton University Press.
Sparks, J., T. Soper. 1990. Parrots: a Natural History . New York, NY: Facts On File Inc.
Rare Species Conservatory Foundation (Pionites lecogaster xanthomeria). A management guide for the white-bellied caique parrot. N/A. Loxahatchee, FL: Rare Species Conservatory Foundation. 1998. Accessed September 25, 2015 at http://www.rarespecies.org/wb.pdf .