The American Flamingo (Phoenicopterus ruber) is a large species of flamingo closely related to the Greater Flamingo and Chilean Flamingo. It was formerly considered conspecific with the Greater Flamingo, but that treatment is now widely viewed (e.g. by the American and British Ornithologists' Unions) as incorrect due to a lack of evidence. It has also been known as the Caribbean Flamingo, but the species' presence in the Galápagos makes that name problematic. It is the only flamingo which naturally inhabits North America.
- 1 Distribution
- 2 Description
- 3 Adaptations
- 4 Osmoregulation
- 5 Circulatory System
- 6 Respiratory System
- 7 Thermoregulation
- 8 Migration
- 9 Metabolism
- 10 References
- 11 Further reading
- 12 External links
The American Flamingo breeds in the Galápagos, coastal Colombia, Venezuela and nearby islands, Trinidad and Tobago, Hispaniola, Cuba, the Turks and Caicos Islands, and along the northern coast of the Yucatán Peninsula. Most sightings in southern Florida are usually considered to be escapees, although at least one bird banded as a chick in the Yucatán Peninsula has been sighted in Everglades National Park, and others may be vagrant birds from Cuba. From a distance, untrained eyes can also confuse the Roseate Spoonbill with it.
Its preferred habitats are similar to that of its relatives: saline lagoons, mudflats, and shallow brackish coastal or inland lakes. An example specific habitat is in the Petenes mangroves ecoregion of the Yucatán.
The American Flaming, like most other mammals is a homeothermic endotherm, which is an animal that basically keeps a consistent temperature that is regulated within its body. Like all flamingos, it lays a single chalky white egg on a mud mound, between May and August; incubation until hatching takes from 28 to 32 days; both parents brood the young for a period of up to 6 years when they reach sexual maturity. Their life expectancy of 40 years is one of the longest in birds.
Adult American Flamingoes are smaller on average than Greater Flamingoes but are the largest flamingoes in the Americas. They measure from 120 to 145 cm (47 to 57 in) tall. The males weigh an average of 2.8 kg (6.2 lb), while females average 2.2 kg (4.9 lb). Most of its plumage is pink, giving rise to its earlier name of Rosy Flamingo and differentiating adults from the much paler Greater Flamingo. The wing coverts are red, and the primary and secondary flight feathers are black. The bill is pink and white with a restricted black tip, and the legs are entirely pink. The call is a goose-like honking.
It is one of the species to which the Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) applies.
From its environment, the American Flamingo has adapted ways at which it can survive. The shallow water that it is usually in, has allowed for the adaptation of its long legs, and large webbed feet in order to wade and stir up the bottom of the water bed to bring up their food source to then be retrieved. In order to feed they have specialized beaks, which are hooked downward and have a marginal lamellae on the upper jaw, and inner and outer lamellae on both the upper and lower jaw for filtering out different sized food from water. Depending on the food source in their area, will depend on the exact morphology of their beaks on what can and cannot be strained out of them. Because it submerges its head under water to retrieve its food, it may have its head under water for larger amounts of time, which requires it to hold its breath. Some factors which affect the habitat area that the American flamingos choose are environmental temperatures, water depth, food source, how accessible an area is and vegetative beds that are in the areas that they feed. If the food requirements don’t meet the needs of the flamingo or the temperatures are not comfortable to their requirements, they move to a better feeding or more temperate area.
The role of osmoregulation, that is maintaining a precise balance of solute and water concentrations within the body, is performed by a melody of bodily functions working together. In Phoenicopterus ruber, the kidney, the lower gastrointestinal tract tract, and the salt glands work together to maintain the homeostasis between ions and fluids. In mammals, the kidneys and urinary bladder are the primary organs used to control osmoregulation; birds, however, lack a urinary bladder and must compensate for this and they do so through the of mechanisms of these three systems.
Phoenicopterus ruber are salt water birds that ingest food with a high salt content and mostly drink salt water (with an osmolarity of usually 1000), hyperosmotic to the bodies cells . As well, not commonly, if the environment permits it they can drink water at near boiling temperatures from geysers for fresh drinking water. From the high salt diet that these birds mostly have, they would lose more water and have a greater salt uptake. One way in which they have adapted a way to maintain osmoregulation is through the use of a salt gland, which is found in their beaks. This salt gland helps emit excess salt from the body through the nasal openings in their beaks. When these birds consume salt, the osmolalrity increases in the blood plasma through the gut, therefore, having water move out of the cells causing an increase in extracellular fluids. Both these changes in turn activate the salt glands of the bird, but before any activity occurs in the salt glands the kidney has to reabsorbed the ingested Na from the small intestine. As seen in other salt-water birds, the fluid that is excreted has been seen to have an osmolarity greater than that of the salt water, but this varies on salt consumption and body size, compared to their bodies which would be much less.
As food and salt water is ingested during feeding sodium and water absorption begins in the gut. It is absorbed through the walls of the gut and into the extracellular fluid. Sodium is then circulated to the kidney where the plasma undergoes filtration by the renal glomerulus. Although bird’s kidneys tend to be larger in size they are inefficient in producing concentrated urine that is significantly hyperosmotic to their blood plasma. This form of secretion would cause dehydration from water loss. Therefore, sodium and water is reabsorbed into the plasma by renal tubules. This increase in osmotic plasma levels causes extracellular fluid volume to increase which triggers receptors in both the brain and heart. These receptors then stimulate salt gland secretion, and sodium is able to efficiently leave the body through the nares while maintaining a high body water level.
Flamingos, like many other marine birds, have a high saline intake, yet even with this in mind the glomular filtration rate (GFR) remains unchanged. This is because of the salt glands; high concentrations of Na is present in the renal filtrate but can be reabsorbed almost completely where it is excreted in high concentrations in the salt glands. Renal reabsorption can be increased through the output of the antidiuretic hormone called arginine vasotacin (AVT). AVT opens protein channels in the collection ducts of the kidney called aquaporins. Aquaporins increase the membrane permeability to water, as well as causes less water to move from the blood and into the kidney tubules.
Specialized Osmoregulatory Cells and Transport Mechanisms
The salt gland used by the American Flamingo (Phoencopterus ruber) has two segments, a medial and lateral segment. These segments are tube shaped glands that consist of two cell types. The first is the cuboidal – peripheral cells which are small, triangular shaped cells which have only a few mitochondria. The second specialized cells are the principal cells which are found down the length of the secretory tubules, and are rich in mitochondria. These cells are similar to the mitochondria rich cells found in teleost fish.
These cells within the salt gland employ several types or transport mechanisms that respond to osmoregulatory loads. Sodium-Potassium ATPase works with a Sodium-Chloride cotransporter (also known as the NKCC), and a basal potassium channel to secrete salt (NaCl) into secretory tubes. The ATPase uses energy from ATP to pump three sodium ions out of the cell and two potassium ions into the cell. The potassium channel allows potassium ions to diffuse out of the cell. The cotransporter pumps one sodium, potassium and two chloride ions in to the cell. The chloride ion diffuses through the apical membrane into the secretory tube and the sodium follows via a paracellular route. This is what forms the hyperosmotic solution within the salt glands.
Although there has been little investigation on the specific circulatory and cardiovascular system of the phoenicopteridae, they possess the typical features of an avian circulatory system. As is seen in other aves, the flamingo’s circulatory system is closed maintaining a separation of oxygenated and deoxygenated blood. This maximizes their efficiency to meet their high metabolic needs during flight. Due to this need for increased cardiac output, the avian heart tends to be larger in relation to body mass than what is seen in most mammals.
Heart Type and Features
The avian circulatory system is driven by a four-chambered, myogenic heart contained in a fibrous pericardial sac. This pericardial sac is filled with a serous fluid for lubrication. The heart itself is divided into a right and left half, each with an atrium and ventricle. The atrium and ventricles of each side are separated by atrioventricular valves which prevent back flow from one chamber to the next during contraction. Being myogenic, the hearts pace is maintained by pacemaker cells found in the sinoatrial node, located on the right atrium. The sinoatrial node uses calcium to cause a depolarizing signal transduction pathway from the atrium through right and left atrioventricular bundle which communicates contraction to the ventricles. The avian heart also consists of muscular arches that are made up of thick bundles of muscular layers. Much like a mammalian heart, the avian heart is composed of endocardial, myocardial and epicardial layers. The atrium walls tend to be thinner than the ventricle walls, due to the intense ventricular contraction used to pump oxygenated blood throughout the body.
Organization of Circulatory System
Similar to the atrium, the arteries are composed of thick elastic muscles to withstand the pressure of the ventricular constriction, and become more rigid as they move away from the heart. Blood moves through the arteries, which undergo vasoconstriction, and into arterioles which act as a transportation system to distribute primarily oxygen as well as nutrients to all tissues of the body. As the arterioles move away from the heart and into individual organs and tissues they are further divided to increase surface area and slow blood flow. Travelling through the arterioles blood moves into the capillaries where gas exchange can occur. Capillaries are organized into capillary beds in tissues, it is here that blood exchanges oxygen for carbon dioxide waste. In the capillary beds blood flow is slowed to allow maximum diffusion of oxygen into the tissues. Once the blood has become deoxygenated it travels through venules then veins and back to the heart. Veins, unlike arteries, are thin and rigid as they do not need to withstand extreme pressure. As blood travels through the venules to the veins a funneling occurs called vasodilation bringing blood back to the heart. Once the blood reaches the heart it moves first into the right atrium, then the left ventricle to be pumped through the lungs for further gas exchange of carbon dioxide waste for oxygen. Oxygenated blood then flows from the lungs through the left atrium to the left ventricle where it is pumped out to the body. With respect to thermoregulation, the American Flamingo has highly vascularized feet that use a countercurrent exchange system in there legs and feet. This method of thermoregulation keeps a constant gradient between the veins and arteries that are in close proximity in order to maintain heat within the core and minimize heat loss or gain in the extremities. Heat loss is minimized while wading in cold water, while heat gain is minimized in the hot temperatures during rest and flight.
Physical and Chemical Properties of Pumping Blood
Avian hearts are generally larger than mammalian hearts when compared to body mass. This adaptation allows more blood to be pumped to meet the high metabolic need associated with flight. Birds, like the flamingo, have a very efficient system for diffusing oxygen into the blood; birds have a ten times greater surface area to gas exchange volume than mammals. As a result, birds have more blood in their capillaries per unit of volume of lung than a mammal. The Flamingo’s (Phoenicopterus Ruber) four chambered heart is myogenic meaning that all the muscle cells and fibers have the ability to contract rhythmically. The rhythm of contraction is controlled by the pace maker cells which have a lower threshold for depolarization. The wave of electrical depolarization initiated here is what physically starts the heart’s contractions and begins pumping blood. Pumping blood creates variations in blood pressure and as a result, creates different thicknesses of blood vessels. The Law of LaPlace can be used to explain why arteries are relatively thick and veins are thin.
Flamingo Blood Composition
It was widely thought that avian blood had special properties which attributed to a very efficient extraction and transportation of oxygen in comparison to mammalian blood. This of course is not true; there is no real difference in the efficiency of the blood, and both mammals and birds use a hemoglobin molecule as the primary oxygen carrier with little to no difference in oxygen carrying capacity. Captivity and age have been seen to have an effect on the blood composition of the American flamingo (Phoenicopterus Ruber). A decrease in white blood cell numbers was predominate with age in both captive and free living flamingos, but captive flamingos showed a higher white blood cell count than free living flamingos. One exception occurs in free living flamingos with regards to white blood cell count. The number of eosinophils in free living birds are higher because these cells are the ones that fight off parasites which a free living bird may have more contact with than a captive one. Captive birds showed higher hematocrit and red blood cell numbers than the free living flamingos, and a blood hemoglobin increase was seen with age. An increase in hemoglobin would correspond with an adults increase in metabolic needs. A smaller mean cellular volume recorded in free living flamingos coupled with similar mean hemoglobin content between captive and free living flamingos could show different oxygen diffusion characteristics between these two groups. Plasma chemistry remains relatively stable with age but lower values of protein content, uric acid, cholesterol, triglycerides, and phospholipids were seen in free living flamingos. This trend can be attributed to shortages and variances in food intake in free living flamingos.
Blood Composition and Osmoregulation
Avian erythrocytes (red blood cells) have been shown to contain approximately ten times the amount of taurine (an amino acid) than mammal erythrocytes. Taurine has a fairly large list of physiological functions; but in birds, it can have an important influence on osmoregulation. Taurine helps the movement of ions in erythrocytes by altering the permeability of the membrane and regulating osmotic pressure within the cell. The regulation of osmotic pressure is achieved by the influx or efflux of taurine relative to changes in the osmolarity of the blood. In a hypotonic environment, cells will swell and eventually shrink; this shrinkage is due to efflux of Taurine. This process also works in the opposite way in hypertonic environments. In hypertonic environments cells tend to shrink and then enlarge; this enlargement is due to an influx in taurine, affectively changing the osmotic pressure. This adaptation allows the flamingo to regulate between differences in salinity.
Relatively few studies have focused on the flamingo respiratory system, however little to no divergences from the standard avian anatomical design have occurred in their evolutionary history. Nevertheless, some physiological differences do occur in the flamingo and structurally similar species.
The respiratory system is not only important for efficient gas exchange, but for thermoregulation and vocalization. Thermoregulation is important for flamingos as they generally live in warm habitats and their plush plumage increases body temperature. Heat loss is accomplished through thermal polypnea (panting), that is an increase in respiratory rate. It has been seen that the medulla, hypothalamus and mid-brain are involved in the control of panting, as well through the Hering-Breuer reflex that uses stretch receptors in the lungs, and the vagus nerve. This effect of the panting is accelerated by a process called gular fluttering; rapid flapping of membranes in the throat which is synchrinized with the movements of the thorax. Both of these mechanisms promote evaporative heat loss, which allows for the bird to push out warm air and water from the body. Increases in respiratory rate would normally cause respiratory alkalosis because carbon dioxide levels are rapidly dropping in the body, but the flamingo is able to bi-pass this, most likely through a shunt mechanism, which allow it to still maintain a sustainable partial pressure of carbon dioxide in the blood. Since the avian integument is not equipped with sweat glands, cutaneous cooling is minimal. Because the flamingo's respiratory system is shared with multiple functions, panting must be controlled to prevent hypoxia.
For a flamingo, having such a long neck means adapting to an unusually long trachea. Tracheas are an important area of the respiratory tract; aside from directing air in and out of the lungs, it has the largest volume of dead space in the tract. Dead space in avians is around 4.5 times higher in mammals of roughly the same size. In particular, flamingos have a trachea that is longer than its body length with 330 cartilaginous rings. As a result, they have a calculated dead space twice as high as another bird of the same size. To compensate for the elongation, they usually breathe in deep, slow patterns.
One hypothesis for the bird’s adaptation to respiratory alkalosis is tracheal coiling. Tracheal coiling is an overly long extension of the trachea and can often wrap around the bird’s body. When faced with a heat load, birds often use thermal panting and this adaptation of tracheal coiling allows ventilation of non-exchange surfaces which can enable the bird to avoid respiratory alkalosis. The flamingo uses a “flushout” pattern of ventilation where deeper breaths are essentially mixed in with shallow panting to flush out carbon dioxide and avoid alkalosis. The increased length of the trachea provides a greater ability for respiratory evaporation and cooling off without hyperventilation.
Thermoregulation is a matter of keeping a consistent body temperature regardless of the surrounding ambient temperature. Flamingos require both methods of efficient heat retention and release. Even though the American flamingo resides mainly close to the equator where there is relatively little fluctuations in temperature, seasonal and circadian variations in temperature must be accounted for.
Like all animals, flamingos maintain a relatively constant basal metabolic rate (BMR); the metabolic rate of an animal in its thermoneutral zone (TNZ) while at rest. The BMR is a static rate which changes depending on factors such as the time of day or seasonal activity. Like most other birds, basic physiological adaptations control both heat loss in warm conditions and heat retention in cooler conditions. Using a system of countercurrent blood flow, heat is efficiently recycled through the body rather than being lost through extremities such as the legs and feet.
Living in the equatorial region of the world the American Flamingo has little variation in seasonal temperature changes. However, as a homeothermic endotherm it is still faced with the challenge of maintaining a constant body temperature while being exposed to both the day (light period) and night (dark period) temperatures of its environments. The Phoenicopterus ruber have evolved a number of thermoregulatory mechanisms to keep itself cool during the light period and warm during the dark period without expending too much energy. The American Flamingo has been observed in a temperature niche between 17.8°C – 35.2°C . In order to prevent water loss through evaporation when temperatures are elevated the flamingo will employ hyperthermia as a nonevaporative heat loss method keeping its body temperature between 40°C and 42°C. This allows heat to leave the body by moving from an area of high body temperature to an area of a lower ambient temperature . Flamingos are also able to use evaporative heat loss methods such as, cutaneous evaporative heat loss and respiratory evaporative heat loss . During cutaneous heat loss, Phoenicopterus ruber relies on evaporation off of the skin to reduce its body temperature. This method is not very efficient as it requires evaporation to pass through the plumage. A more efficient way to reduce its body temperature is through respiratory evaporative heat loss, where the flamingo engages in panting to expel excessive body heat . During the dark period the flamingos tend to tuck their heads beneath their wing to conserve body heat. They may also elicit shivering as a means of muscular energy consumption to produce heat as needed.
One of the most distinctive attribute of P. ruber is its unipedal stance, or the tendency to stand on one leg. While the purpose of this iconic posture remains ultimately unanswered, strong evidence supports its function in regulating body temperature. Like most birds, the largest amount of heat is lost through the legs and feet; having long legs can be a major disadvantage when temperatures fall and heat retention is most important. By holding one leg up against the ventral surface of the body, the flamingo lowers the surface area by which heat exits the body. Moreover, it has been observed that during periods of increased temperatures such as mid-day, flamingos will stand on both legs. Holding a bipedal stance multiplies the amount of heat lost from the legs and further regulates body temperature.
Like other flamingo species, American flamingos will migrate short distances to ensure that they get enough food or because their current habitat has been disturbed in some way.One habitat disturbance that has been observed to cause flamingos to leaving their feeding grounds is elevated water levels. These conditions make it difficult for the Phoenicopterus ruber to wade, hindering their ability to access food. The flamingos will then abandon their feeding grounds in search of an alternate food source. . While the flights are not as long as other migratory birds flamingos still fly for periods without eating. 
For the most part flamingos are not all that different from other salt water wading birds. They will fast when migrating to a new habitat or the chicks may not receive food daily depending on food availability.
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|Wikimedia Commons has media related to Phoenicopterus ruber.|
- Caribbean Flamingo from the IUCN/Wetlands International Flamingo Specialist Group
- Flamingo Resource Centre - a collection of resources and information related to flamingos
- 3D computed tomographic animations showing the anatomy of the head of the Caribbean Flamingo