Geographic Range
Agami herons (
Agamia agami
) occur primarily in South America, with their core distribution in the Orinoco and
Amazon basins. Sightings have been recorded as far north as southern Veracruz and
Neuvo Leon, Mexico. Their range also extends from eastern Mexico in the north, through
Guatemala, Belize, El Salvador, Honduras, Nicaragua and Costa Rica. The southernmost
border of their distribution is found along the western coastal strip of South America.
Agami herons have been observed in Panama between the months of January and June,
suggesting dry season migration.
- Biogeographic Regions
- neotropical
- atlantic ocean
Habitat
Agami herons occupy inland wetland habitats. Forested swamps are particularly favored
by the herons due to its diverse, wading-friendly foraging habitat, it also provides
the trees and bushes necessary for roosting and nesting. More specifically, Agami
herons dwell in dense tropical lowland forests, typically along the margins of small
rivers, swamps and estuary streams. Studies have demonstrated that their distribution
is most closely linked to the margins of isolated bodies of water. Agami herons are
also known to use mangroves.
- Habitat Regions
- temperate
- tropical
- freshwater
- Terrestrial Biomes
- chaparral
- scrub forest
- Aquatic Biomes
- rivers and streams
- temporary pools
- brackish water
- Other Habitat Features
- estuarine
Physical Description
These herons are medium-sized; they typically weigh between 0.1 and 4.5 kg and are
0.6 to 0.76 meters tall. Agami herons are short-statured and exhibit a crouched-like
appearance. Their bill is rapier-like and is typically 13.9 cm in length, which represents
one-fifth of their total body length. Agami herons have been characterized as having
striking, dichromatic plumage. Adults have prominent, sickle-shaped plumage on each
side of their head. Their abdominal region is chestnut-brown while their wings are
dark teal, with brown streaks on both their ventral and dorsal surfaces. Their wings
are broad, spanning 100 cm, with 9 to 11 primary feathers. Their tail feathers are
short and light-brown in coloration. Males and females differ only slightly in their
coloring and size, although males do tend to have more brilliantly colored plumage.
Juveniles have darkened, cinnamon-striped abdominal plumage, which is reduced to chestnut-brown
in adulthood. Juveniles also possess light blue feathers surrounding their crown.
- Other Physical Features
- endothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
- male more colorful
- ornamentation
Reproduction
Agami herons are serially monogamous. While herons generally return to the same site
to nest year after year, it is not known if Agami herons participate in life-long
partnerships, or return to find new mates. They are known to nest in mixed or single
species colonies, classifying them as social, colonial nesters. For social nesters,
despite monogamous pairing, promiscuous mating behavior may be common. It is not known
whether Agami herons participate in extra pair copulations, however, it is suspected.
Males tend to arrive at colony sites to claim nesting territory. During the breeding
season, males display wispy, light-blue crest feathers and broad light-blue plumes
on the lower backside of their body, which they often puff out and shake to attract
potential mates. During the mating display, males lift their head to a vertical position
and bring it down abruptly in a bobbing fashion; this is often followed by snapping
their bill. Later in the nesting season, this type of communication is used between
mating pairs in social interaction and in mate recognition. Once pairs are established,
both males and females work together to build nests. Males are largely responsible
for defending the nest territory.
- Mating System
- monogamous
Agami herons nest primarily in the wet season, between the months of June and September.
Nests can be found in bushes and trees over water and under the dense cover of the
canopy. Specific locations for nests include isolated clumps of mangroves, dead tree
branches of drowned trees in artificial lakes, trees standing in water and bushes
within marshes. Agami herons prefer to keep nests well hidden within terrestrial vegetation.
Nests themselves average 15 cm in diameter and 8 cm in height and are characterized
by loose, thick, platform twigs. Clutch sizes range from 2 to 4 light blue eggs. Little
is known about their incubation period; however, the incubation time of other herons
is approximately 26 days. Time to fledgling is approximately 2 to 3 weeks and time
to independence is about 6 to 7 weeks. The exact age when sexual maturity is reached
in Agami herons is not known, however, it is estimated to be between 2 to 3 years.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Prior to fertilization, male herons participate in building nests, while building,
males defend their nesting territory. Agami herons incubate and shade their eggs during
daylight hours. Both parents take turns brooding the nest. The total brooding time
ranges from 1 to 2 weeks. One parent forages for food while the other watches over
the nest. Feeding birds leave and return to the nesting colony individually, and do
so during the night. Research suggests that nesting Agami herons leave to feed in
the swamps and savannas between the coastal mangrove forests and travel up to 100
km from their nest to feed. When returning to the nesting colony, adults make short,
loud calls, and in response, chicks give a high-pitched answer; this is known as the
"Chup" call. Incubation begins before the clutch is completed and young hatch at different
times. The oldest chick dominates over the younger chicks in competition for food.
- Parental Investment
- altricial
- male parental care
- female parental care
-
pre-fertilization
-
protecting
- male
-
protecting
-
pre-hatching/birth
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
-
pre-independence
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
Lifespan/Longevity
Little is known about the lifespan of Agami herons. It has been estimated that they
live approximately 13 years, which is common for members of family
Ardeidae
(herons, egrets). Their lifespan in captivity has not been measured. The oldest documented
individual lived 16 years.
Behavior
Little is known about the behavior of Agami herons, apart from their mating behavior.
However, they are often observed standing in a crouched position on banks, dykes,
bushes or branches overhanging the water while foraging. They also have been documented
walking slowly in shallow water at the edge of streams or ponds when hunting for fish.
They rattle off a low-pitched alarm call when threatened. They spend most of their
time, apart from nesting season, alone as solitary foragers. Due to the rare sightings
of Agami herons, it has been hypothesized that when they are not foraging, they spend
most of their time hidden in the canopies of trees. The solitary and evasive nature
of Agami herons makes them difficult to observe from long distances. Their exact migratory
patterns have yet to be documented; however, it has been proposed that they do not
take part in long distance travel due to their ability to co-exist with other species
of heron that lack their distinct bill and body morphology.
Home Range
Male Agami herons are known to show territorial behavior when guarding a specific
colonial area during mating season. The exact dimensions of the territory are not
known, however, their home ranges may be relatively large due to their solitary foraging
outside of mating season.
Communication and Perception
Agami herons are widely known for their distinct, low-pitched alarm call, which is
used in response to threats. Their alarm call may also be used between mates as communication
while nesting. In addition, males also use head-bobbing, bill clacking and calling
as methods of attracting a mate. Research suggests that the pattern of such head-bobbing
and bill clacking is used in mate to mate recognition while nesting and in defending
nest territory. Upon arrival to the colony during nesting season, adults make a short,
loud call, and in response, chicks make a high-pitched answer call. The characteristic
social call of Agami herons is a low-pitched rattle called the "Gr" call. The "Gr"
call has been characterized and described as a pig-like, low-pitched rattle.
- Communication Channels
- acoustic
Food Habits
Agami herons are specialized bank fishers. Their morphological adaptations have allowed
them to effectively forage in shallow water on grassy shores. Their short legs and
long neck give them the power to produce a long, lunging strike at prey items. They
are solitary feeders, with individuals often scattered along water courses. With their
long neck and bill, they are primarily piscivorous, feeding on a variety of fish.
Agami herons are also known to employ a wading technique of foraging, which mixes
standing still and slowly wading, usually in a deep crouch with the ventral feathers
of their neck touching the water. Agami herons consume prey ranging between 2 to 20
cm. The majority of their prey consists of characins (
Triportheus angulatus
and
Astyanax angulatus
) which are surface-swimming fishes. Less commonly, they have also been known to consume
cichlids (
Aequindens
).
- Animal Foods
- amphibians
- fish
- other marine invertebrates
Predation
Dichromatic plumage appears to help make Agami herons cryptic to predators; however,
their method of solitary foraging may expose them to predation. Their predators include
common black hawks
and
American crocodiles
.
- Anti-predator Adaptations
- cryptic
Ecosystem Roles
Little is known of the role Agami herons play in the Neotropical ecosystem. Research
suggests that all species belonging to the family
Ardeidae
contribute to the maintenance of fish diversity in streams by consuming highly abundant
surface-feeding fish. Approximately 64.8% of all birds living in Guyana possess avian
Hematazoa; however, specific parasites of Agami herons have yet to be analyzed.
Economic Importance for Humans: Positive
The ways in which humans benefit from the ecosystem functions of Agami herons is unknown.
However, humans have harvested herons' colorful plumes to sell at markets. Documents
dating back to the 1800's suggest that plumes were harvested and made into expensive
head pieces in tropical South American villages. In addition, eggs are harvested for
food by some native populations.
- Positive Impacts
- food
- body parts are source of valuable material
Economic Importance for Humans: Negative
There are no known negative economic impacts of Agami herons on humans.
Conservation Status
Current threats to Agami herons include deforestation in the Amazon basin. Deforestation
models predict that Agami herons will lose between 18.6 to 25.6% of their suitable
habitat. Conservation activity at this time has not been specified, however, proposals
have been made to conserve the herons' habitat and expand protected area networks
to be more inclusive of IBAs (Important Bird Areas). Due to the exclusivity and hidden
nature of Agami herons' habitat, conservationists are aiming to expand market pressures
for responsible land management. Limiting the use of unsuitable land for agricultural
ventures has been the main focus in maintaining the herons' habitat.
Other Comments
Herons date back to the Eocene Era, 60 to 38 million years ago. Herons are often not
represented in the fossil record prior to the Pleistocene due to the slight structure
of their skeletons. Agami herons, along with boat-billed herons (
Cochlearius cochlearius
) and tiger herons (
Tigrisoma
), are considered the remnants of the basal lineage of
Ardeidae
. Agami herons are currently recognized as the only representative of their subfamily.
Additional Links
Contributors
Wendy Forrest (author), Indiana University-Purdue University Fort Wayne, Mark Jordan (editor), Indiana University-Purdue University Fort Wayne, Leila Siciliano Martina (editor), Texas State University.
- 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.
- Atlantic Ocean
-
the body of water between Africa, Europe, the southern ocean (above 60 degrees south latitude), and the western hemisphere. It is the second largest ocean in the world after the Pacific Ocean.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- temperate
-
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
- tropical
-
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
- freshwater
-
mainly lives in water that is not salty.
- chaparral
-
Found in coastal areas between 30 and 40 degrees latitude, in areas with a Mediterranean climate. Vegetation is dominated by stands of dense, spiny shrubs with tough (hard or waxy) evergreen leaves. May be maintained by periodic fire. In South America it includes the scrub ecotone between forest and paramo.
- scrub forest
-
scrub forests develop in areas that experience dry seasons.
- brackish water
-
areas with salty water, usually in coastal marshes and estuaries.
- marsh
-
marshes are wetland areas often dominated by grasses and reeds.
- swamp
-
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
- estuarine
-
an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.
- sexual ornamentation
-
one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.
- 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.
- nomadic
-
generally wanders from place to place, usually within a well-defined range.
- solitary
-
lives alone
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- acoustic
-
uses sound to communicate
- cryptic
-
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
- food
-
A substance that provides both nutrients and energy to a living thing.
- carnivore
-
an animal that mainly eats meat
- piscivore
-
an animal that mainly eats fish
- 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.
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
References
Caldwell, G. 1986. Predation as a Selective Force on Foraging Herons: Effects of Plumage Color and Flocking. The Auk , Volume 103, Issue 3: "494-505".
Cintra, R. 2012. Ecological Gradients Influencing Waterbird Communities in Black Water Lakes in the Anavilhanas Archipelago, Central Amazonia. International Journal of Ecology , Volume 1, Issue 1: "1-21".
Dittmann, D., S. Cardiff. 2009. Herons. Pp. 59-61 in National Geographic Complete Birds of the World , Vol. 1. Washington, D.C: The National Geographic Society.
Durrant, K., J. Beadell, F. Ishtiaq. 2006. Avian Hematozoa in South America: A Comparison of Temperate and Tropic Zones. Ornithological Monographs , Volume 60: "102".
Garza-Torres, H., R. Herrera-Herrera, G. Escalona-Segura, J. Vargas-Contreras, A. Navarro. 2003. New Bird Records from Tamaulipas, Mexico. The Southwestern Naturalist , Vol. 48, Issue 4: "707-710".
Gonzalez, J. 1999. Effects of Harvesting of Waterbirds and Their Eggs by Native People in the Northeastern Peruvian Amazon. Waterbirds , Volume 22, Issue 2: "217-224".
Hancock, J., J. Kushlan. 1984. The Herons Handbook . London, England: Christopher Helm Publishers.
Hancock, J. 1999. Herons & Egrets Of The World: A Photographic Journey . San Diego: Academic Press.
Howell, S., S. Webb. 1995. A Guide to the Birds of Mexico and Northern Central America . New York, New York: Oxford University Press.
Lees, A. 2011. Integrating Spatially Explicit Habitat Projections Into Extinction Risk Assessments: A Reassessment of Amazonian Avifauna Incorporating Projected Deforestation. Diversity and Distributions , Volume 18, Issue 3: "273-281".
Marin, M. 1982. Notes on the Breeding of the Chestnut-Bellied Heron ( Agamia agami ) in Venezuela. The Auk , 99, Issue 4: "784".
Reynaud, P., J. Kushlan. 2004. Nesting of the Agami Heron. Waterbirds: The International Journal of Waterbird Biology , Vol. 17, Issue 4: "308-311".
Willard, D. 1985. Comparative Ecology of Twenty-Two Tropical Piscivores. Orinthological Monographs , Vol. 36: "788-797".
Gale, Cengage Learning. 2003. Herons and Bitterns ( Ardeidae ). Pp. "239-260" in Grizmek's Animal Life Encyclopedia , Vol. 8: Issue I, 2nd Edition. Detroit: Gale.